G0000–G9999: Procedures/Professional Services

HCPC SEQNUM RECID LONG DESCRIPTION SHORT DESCRIPTION
G0008 0010 3 Administration of influenza virus vaccine Admin influenza virus vac
G0009 0010 3 Administration of pneumococcal vaccine Admin pneumococcal vaccine
G0010 0010 3 Administration of hepatitis b vaccine Admin hepatitis b vaccine
G0027 0010 3 Semen analysis; presence and/or motility of sperm excluding huhner Semen analysis
G0068 0010 3 Professional services for the administration of anti-infective, pain management, chelation, pulmonary hypertension, and/or inotropic infusion drug(s) for each infusion drug administration calendar day in the individual’s home, each 15 minutes Adm of infusion drug in home
G0069 0010 3 Professional services for the administration of subcutaneous immunotherapy for each infusion drug administration calendar day in the individual’s home, each 15 minutes Adm of immune drug in home
G0070 0010 3 Professional services for the administration of chemotherapy for each infusion drug administration calendar day in the individual’s home, each 15 minutes Adm of chemo drug in home
G0071 0010 3 Payment for communication technology-based services for 5 minutes or more of a virtual (non-face-to-face) communication between an rural health clinic (rhc) or federally qualified health center (fqhc) practitioner and rhc or fqhc patient, or 5 minutes or more of remote evaluation of recorded video and/or images by an rhc or fqhc practitioner, occurring in lieu of an office visit; rhc or fqhc only Comm svcs by rhc/fqhc 5 min
G0076 0010 3 Brief (20 minutes) care management home visit for a new patient. for use only in a medicare-approved cmmi model. (services must be furnished within a beneficiary’s home, domiciliary, rest home, assisted living and/or nursing facility) Care manag h vst new pt 20 m
G0077 0010 3 Limited (30 minutes) care management home visit for a new patient. for use only in a medicare-approved cmmi model. (services must be furnished within a beneficiary’s home, domiciliary, rest home, assisted living and/or nursing facility) Care manag h vst new pt 30 m
G0078 0010 3 Moderate (45 minutes) care management home visit for a new patient. for use only in a medicare-approved cmmi model. (services must be furnished within a beneficiary’s home, domiciliary, rest home, assisted living and/or nursing facility) Care manag h vst new pt 45 m
G0079 0010 3 Comprehensive (60 minutes) care management home visit for a new patient. for use only in a medicare-approved cmmi model. (services must be furnished within a beneficiary’s home, domiciliary, rest home, assisted living and/or nursing facility) Care manag h vst new pt 60 m
G0080 0010 3 Extensive (75 minutes) care management home visit for a new patient. for use only in a medicare-approved cmmi model. (services must be furnished within a beneficiary’s home, domiciliary, rest home, assisted living and/or nursing facility) Care manag h vst new pt 75 m
G0081 0010 3 Brief (20 minutes) care management home visit for an existing patient. for use only in a medicare-approved cmmi model. (services must be furnished within a beneficiary’s home, domiciliary, rest home, assisted living and/or nursing facility) Care man h v ext pt 20 mi
G0082 0010 3 Limited (30 minutes) care management home visit for an existing patient. for use only in a medicare-approved cmmi model. (services must be furnished within a beneficiary’s home, domiciliary, rest home, assisted living and/or nursing facility) Care man h v ext pt 30 m
G0083 0010 3 Moderate (45 minutes) care management home visit for an existing patient. for use only in a medicare-approved cmmi model. (services must be furnished within a beneficiary’s home, domiciliary, rest home, assisted living and/or nursing facility) Care man h v ext pt 45 m
G0084 0010 3 Comprehensive (60 minutes) care management home visit for an existing patient. for use only in a medicare-approved cmmi model. (services must be furnished within a beneficiary’s home, domiciliary, rest home, assisted living and/or nursing facility) Care man h v ext pt 60 m
G0085 0010 3 Extensive (75 minutes) care management home visit for an existing patient. for use only in a medicare-approved cmmi model. (services must be furnished within a beneficiary’s home, domiciliary, rest home, assisted living and/or nursing facility) Care man h v ext pt 75 m
G0086 0010 3 Limited (30 minutes) care management home care plan oversight. for use only in a medicare-approved cmmi model. (services must be furnished within a beneficiary’s home, domiciliary, rest home, assisted living and/or nursing facility) Care man home care plan 30 m
G0087 0010 3 Comprehensive (60 minutes) care management home care plan oversight. for use only in a medicare-approved cmmi model. (services must be furnished within a beneficiary’s home, domiciliary, rest home, assisted living and/or nursing facility) Care man home care plan 60 m
G0101 0010 3 Cervical or vaginal cancer screening; pelvic and clinical breast examination Ca screen;pelvic/breast exam
G0102 0010 3 Prostate cancer screening; digital rectal examination Prostate ca screening; dre
G0103 0010 3 Prostate cancer screening; prostate specific antigen test (psa) Psa screening
G0104 0010 3 Colorectal cancer screening; flexible sigmoidoscopy Ca screen;flexi sigmoidscope
G0105 0010 3 Colorectal cancer screening; colonoscopy on individual at high risk Colorectal scrn; hi risk ind
G0106 0010 3 Colorectal cancer screening; alternative to g0104, screening sigmoidoscopy, barium enema Colon ca screen;barium enema
G0108 0010 3 Diabetes outpatient self-management training services, individual, per 30 minutes Diab manage trn per indiv
G0109 0010 3 Diabetes outpatient self-management training services, group session (2 or more), per 30 minutes Diab manage trn ind/group
G0117 0010 3 Glaucoma screening for high risk patients furnished by an optometrist or ophthalmologist Glaucoma scrn hgh risk direc
G0118 0010 3 Glaucoma screening for high risk patient furnished under the direct supervision of an optometrist or ophthalmologist Glaucoma scrn hgh risk direc
G0120 0010 3 Colorectal cancer screening; alternative to g0105, screening colonoscopy, barium enema. Colon ca scrn; barium enema
G0121 0010 3 Colorectal cancer screening; colonoscopy on individual not meeting criteria for high risk Colon ca scrn not hi rsk ind
G0122 0010 3 Colorectal cancer screening; barium enema Colon ca scrn; barium enema
G0123 0010 3 Screening cytopathology, cervical or vaginal (any reporting system), collected in preservative fluid, automated thin layer preparation, screening by cytotechnologist under physician supervision Screen cerv/vag thin layer
G0124 0010 3 Screening cytopathology, cervical or vaginal (any reporting system), collected in preservative fluid, automated thin layer preparation, requiring interpretation by physician Screen c/v thin layer by md
G0127 0010 3 Trimming of dystrophic nails, any number Trim nail(s)
G0128 0010 3 Direct (face-to-face with patient) skilled nursing services of a registered nurse provided in a comprehensive outpatient rehabilitation facility, each 10 minutes beyond the first 5 minutes Corf skilled nursing service
G0129 0010 3 Occupational therapy services requiring the skills of a qualified occupational therapist, furnished as a component of a partial hospitalization treatment program, per session (45 minutes or more) Partial hosp prog service
G0130 0010 3 Single energy x-ray absorptiometry (sexa) bone density study, one or more sites; appendicular skeleton (peripheral) (e.g., radius, wrist, heel) Single energy x-ray study
G0141 0010 3 Screening cytopathology smears, cervical or vaginal, performed by automated system, with manual rescreening, requiring interpretation by physician Scr c/v cyto,autosys and md
G0143 0010 3 Screening cytopathology, cervical or vaginal (any reporting system), collected in preservative fluid, automated thin layer preparation, with manual screening and rescreening by cytotechnologist under physician supervision Scr c/v cyto,thinlayer,rescr
G0144 0010 3 Screening cytopathology, cervical or vaginal (any reporting system), collected in preservative fluid, automated thin layer preparation, with screening by automated system, under physician supervision Scr c/v cyto,thinlayer,rescr
G0145 0010 3 Screening cytopathology, cervical or vaginal (any reporting system), collected in preservative fluid, automated thin layer preparation, with screening by automated system and manual rescreening under physician supervision Scr c/v cyto,thinlayer,rescr
G0147 0010 3 Screening cytopathology smears, cervical or vaginal, performed by automated system under physician supervision Scr c/v cyto, automated sys
G0148 0010 3 Screening cytopathology smears, cervical or vaginal, performed by automated system with manual rescreening Scr c/v cyto, autosys, rescr
G0151 0010 3 Services performed by a qualified physical therapist in the home health or hospice setting, each 15 minutes Hhcp-serv of pt,ea 15 min
G0152 0010 3 Services performed by a qualified occupational therapist in the home health or hospice setting, each 15 minutes Hhcp-serv of ot,ea 15 min
G0153 0010 3 Services performed by a qualified speech-language pathologist in the home health or hospice setting, each 15 minutes Hhcp-svs of s/l path,ea 15mn
G0154 0010 3 Direct skilled nursing services of a licensed nurse (lpn or rn) in the home health or hospice setting, each 15 minutes Hhcp-svs of rn,ea 15 min
G0155 0010 3 Services of clinical social worker in home health or hospice settings, each 15 minutes Hhcp-svs of csw,ea 15 min
G0156 0010 3 Services of home health/hospice aide in home health or hospice settings, each 15 minutes Hhcp-svs of aide,ea 15 min
G0157 0010 3 Services performed by a qualified physical therapist assistant in the home health or hospice setting, each 15 minutes Hhc pt assistant ea 15
G0158 0010 3 Services performed by a qualified occupational therapist assistant in the home health or hospice setting, each 15 minutes Hhc ot assistant ea 15
G0159 0010 3 Services performed by a qualified physical therapist, in the home health setting, in the establishment or delivery of a safe and effective physical therapy maintenance program, each 15 minutes Hhc pt maint ea 15 min
G0160 0010 3 Services performed by a qualified occupational therapist, in the home health setting, in the establishment or delivery of a safe and effective occupational therapy maintenance program, each 15 minutes Hhc occup therapy ea 15
G0161 0010 3 Services performed by a qualified speech-language pathologist, in the home health setting, in the establishment or delivery of a safe and effective speech-language pathology maintenance program, each 15 minutes Hhc slp ea 15 min
G0162 0010 3 Skilled services by a registered nurse (rn) for management and evaluation of the plan of care; each 15 minutes (the patient’s underlying condition or complication requires an rn to ensure that essential non-skilled care achieves its purpose in the home health or hospice setting) Hhc rn e&m plan svs, 15 min
G0163 0010 3 Skilled services of a licensed nurse (lpn or rn) for the observation and assessment of the patient’s condition, each 15 minutes (the change in the patient’s condition requires skilled nursing personnel to identify and evaluate the patient’s need for possible modification of treatment in the home health or hospice setting) Hhc lpn/rn obs/asses ea 15
G0164 0010 3 Skilled services of a licensed nurse (lpn or rn), in the training and/or education of a patient or family member, in the home health or hospice setting, each 15 minutes Hhc lis nurse train ea 15
G0166 0010 3 External counterpulsation, per treatment session Extrnl counterpulse, per tx
G0168 0010 3 Wound closure utilizing tissue adhesive(s) only Wound closure by adhesive
G0173 0010 3 Linear accelerator based stereotactic radiosurgery, complete course of therapy in one session Linear acc stereo radsur com
G0175 0010 3 Scheduled interdisciplinary team conference (minimum of three exclusive of patient care nursing staff) with patient present Opps service,sched team conf
G0176 0010 3 Activity therapy, such as music, dance, art or play therapies not for recreation, related to the care and treatment of patient’s disabling mental health problems, per session (45 minutes or more) Opps/php;activity therapy
G0177 0010 3 Training and educational services related to the care and treatment of patient’s disabling mental health problems per session (45 minutes or more) Opps/php; train & educ serv
G0179 0010 3 Physician re-certification for medicare-covered home health services under a home health plan of care (patient not present), including contacts with home health agency and review of reports of patient status required by physicians to affirm the initial implementation of the plan of care that meets patient’s needs, per re-certification period Md recertification hha pt
G0180 0010 3 Physician certification for medicare-covered home health services under a home health plan of care (patient not present), including contacts with home health agency and review of reports of patient status required by physicians to affirm the initial implementation of the plan of care that meets patient’s needs, per certification period Md certification hha patient
G0181 0010 3 Physician supervision of a patient receiving medicare-covered services provided by a participating home health agency (patient not present) requiring complex and multidisciplinary care modalities involving regular physician development and/or revision of care plans, review of subsequent reports of patient status, review of laboratory and other studies, communication (including telephone calls) with other health care professionals involved in the patient’s care, integration of new information into the medical treatment plan and/or adjustment of medical therapy, within a calendar month, 30 minutes or more Home health care supervision
G0182 0010 3 Physician supervision of a patient under a medicare-approved hospice (patient not present) requiring complex and multidisciplinary care modalities involving regular physician development and/or revision of care plans, review of subsequent reports of patient status, review of laboratory and other studies, communication (including telephone calls) with other health care professionals involved in the patient’s care, integration of new information into the medical treatment plan and/or adjustment of medical therapy, within a calendar month, 30 minutes or more Hospice care supervision
G0186 0010 3 Destruction of localized lesion of choroid (for example, choroidal neovascularization); photocoagulation, feeder vessel technique (one or more sessions) Dstry eye lesn,fdr vssl tech
G0202 0010 3 Screening mammography, bilateral (2-view study of each breast), including computer-aided detection (cad) when performed Scr mammo bi incl cad
G0204 0010 3 Diagnostic mammography, including computer-aided detection (cad) when performed; bilateral Dx mammo incl cad bi
G0206 0010 3 Diagnostic mammography, including computer-aided detection (cad) when performed; unilateral Dx mammo incl cad uni
G0219 0010 3 Pet imaging whole body; melanoma for non-covered indications Pet img wholbod melano nonco
G0235 0010 3 Pet imaging, any site, not otherwise specified Pet not otherwise specified
G0237 0010 3 Therapeutic procedures to increase strength or endurance of respiratory muscles, face to face, one on one, each 15 minutes (includes monitoring) Therapeutic procd strg endur
G0238 0010 3 Therapeutic procedures to improve respiratory function, other than described by g0237, one on one, face to face, per 15 minutes (includes monitoring) Oth resp proc, indiv
G0239 0010 3 Therapeutic procedures to improve respiratory function or increase strength or endurance of respiratory muscles, two or more individuals (includes monitoring) Oth resp proc, group
G0245 0010 3 Initial physician evaluation and management of a diabetic patient with diabetic sensory neuropathy resulting in a loss of protective sensation (lops) which must include: (1) the diagnosis of lops, (2) a patient history, (3) a physical examination that consists of at least the following elements: (a) visual inspection of the forefoot, hindfoot and toe web spaces, (b) evaluation of a protective sensation, (c) evaluation of foot structure and biomechanics, (d) evaluation of vascular status and skin integrity, and (e) evaluation and recommendation of footwear and (4) patient education Initial foot exam pt lops
G0246 0010 3 Follow-up physician evaluation and management of a diabetic patient with diabetic sensory neuropathy resulting in a loss of protective sensation (lops) to include at least the following: (1) a patient history, (2) a physical examination that includes: (a) visual inspection of the forefoot, hindfoot and toe web spaces, (b) evaluation of protective sensation, (c) evaluation of foot structure and biomechanics, (d) evaluation of vascular status and skin integrity, and (e) evaluation and recommendation of footwear, and (3) patient education Followup eval of foot pt lop
G0247 0010 3 Routine foot care by a physician of a diabetic patient with diabetic sensory neuropathy resulting in a loss of protective sensation (lops) to include, the local care of superficial wounds (i.e. superficial to muscle and fascia) and at least the following if present: (1) local care of superficial wounds, (2) debridement of corns and calluses, and (3) trimming and debridement of nails Routine footcare pt w lops
G0248 0010 3 Demonstration, prior to initiation of home inr monitoring, for patient with either mechanical heart valve(s), chronic atrial fibrillation, or venous thromboembolism who meets medicare coverage criteria, under the direction of a physician; includes: face-to-face demonstration of use and care of the inr monitor, obtaining at least one blood sample, provision of instructions for reporting home inr test results, and documentation of patient’s ability to perform testing and report results Demonstrate use home inr mon
G0249 0010 3 Provision of test materials and equipment for home inr monitoring of patient with either mechanical heart valve(s), chronic atrial fibrillation, or venous thromboembolism who meets medicare coverage criteria; includes: provision of materials for use in the home and reporting of test results to physician; testing not occurring more frequently than once a week; testing materials, billing units of service include 4 tests Provide inr test mater/equip
G0250 0010 3 Physician review, interpretation, and patient management of home inr testing for patient with either mechanical heart valve(s), chronic atrial fibrillation, or venous thromboembolism who meets medicare coverage criteria; testing not occurring more frequently than once a week; billing units of service include 4 tests Md inr test revie inter mgmt
G0251 0010 3 Linear accelerator based stereotactic radiosurgery, delivery including collimator changes and custom plugging, fractionated treatment, all lesions, per session, maximum five sessions per course of treatment Linear acc based stero radio
G0252 0010 3 Pet imaging, full and partial-ring pet scanners only, for initial diagnosis of breast cancer and/or surgical planning for breast cancer (e.g., initial staging of axillary lymph nodes) Pet imaging initial dx
G0255 0010 3 Current perception threshold/sensory nerve conduction test, (snct) per limb, any nerve Current percep threshold tst
G0257 0010 3 Unscheduled or emergency dialysis treatment for an esrd patient in a hospital outpatient department that is not certified as an esrd facility Unsched dialysis esrd pt hos
G0259 0010 3 Injection procedure for sacroiliac joint; arthrography Inject for sacroiliac joint
G0260 0010 3 Injection procedure for sacroiliac joint; provision of anesthetic, steroid and/or other therapeutic agent, with or without arthrography Inj for sacroiliac jt anesth
G0268 0010 3 Removal of impacted cerumen (one or both ears) by physician on same date of service as audiologic function testing Removal of impacted wax md
G0269 0010 3 Placement of occlusive device into either a venous or arterial access site, post surgical or interventional procedure (e.g., angioseal plug, vascular plug) Occlusive device in vein art
G0270 0010 3 Medical nutrition therapy; reassessment and subsequent intervention(s) following second referral in same year for change in diagnosis, medical condition or treatment regimen (including additional hours needed for renal disease), individual, face to face with the patient, each 15 minutes Mnt subs tx for change dx
G0271 0010 3 Medical nutrition therapy, reassessment and subsequent intervention(s) following second referral in same year for change in diagnosis, medical condition, or treatment regimen (including additional hours needed for renal disease), group (2 or more individuals), each 30 minutes Group mnt 2 or more 30 mins
G0276 0010 3 Blinded procedure for lumbar stenosis, percutaneous image-guided lumbar decompression (pild) or placebo-control, performed in an approved coverage with evidence development (ced) clinical trial Pild/placebo control clin tr
G0277 0010 3 Hyperbaric oxygen under pressure, full body chamber, per 30 minute interval Hbot, full body chamber, 30m
G0278 0010 3 Iliac and/or femoral artery angiography, non-selective, bilateral or ipsilateral to catheter insertion, performed at the same time as cardiac catheterization and/or coronary angiography, includes positioning or placement of the catheter in the distal aorta or ipsilateral femoral or iliac artery, injection of dye, production of permanent images, and radiologic supervision and interpretation (list separately in addition to primary procedure) Iliac art angio,cardiac cath
G0279 0010 3 Diagnostic digital breast tomosynthesis, unilateral or bilateral (list separately in addition to 77065 or 77066) Tomosynthesis, mammo
G0281 0010 3 Electrical stimulation, (unattended), to one or more areas, for chronic stage iii and stage iv pressure ulcers, arterial ulcers, diabetic ulcers, and venous stasis ulcers not demonstrating measurable signs of healing after 30 days of conventional care, as part of a therapy plan of care Elec stim unattend for press
G0282 0010 3 Electrical stimulation, (unattended), to one or more areas, for wound care other than described in g0281 Elect stim wound care not pd
G0283 0010 3 Electrical stimulation (unattended), to one or more areas for indication(s) other than wound care, as part of a therapy plan of care Elec stim other than wound
G0288 0010 3 Reconstruction, computed tomographic angiography of aorta for surgical planning for vascular surgery Recon, cta for surg plan
G0289 0010 3 Arthroscopy, knee, surgical, for removal of loose body, foreign body, debridement/shaving of articular cartilage (chondroplasty) at the time of other surgical knee arthroscopy in a different compartment of the same knee Arthro, loose body + chondro
G0293 0010 3 Noncovered surgical procedure(s) using conscious sedation, regional, general or spinal anesthesia in a medicare qualifying clinical trial, per day Non-cov surg proc,clin trial
G0294 0010 3 Noncovered procedure(s) using either no anesthesia or local anesthesia only, in a medicare qualifying clinical trial, per day Non-cov proc, clinical trial
G0295 0010 3 Electromagnetic therapy, to one or more areas, for wound care other than described in g0329 or for other uses Electromagnetic therapy onc
G0296 0010 3 Counseling visit to discuss need for lung cancer screening using low dose ct scan (ldct) (service is for eligibility determination and shared decision making) Visit to determ ldct elig
G0297 0010 3 Low dose ct scan (ldct) for lung cancer screening Ldct for lung ca screen
G0299 0010 3 Direct skilled nursing services of a registered nurse (rn) in the home health or hospice setting, each 15 minutes Hhs/hospice of rn ea 15 min
G0300 0010 3 Direct skilled nursing services of a licensed practical nurse (lpn) in the home health or hospice setting, each 15 minutes Hhs/hospice of lpn ea 15 min
G0302 0010 3 Pre-operative pulmonary surgery services for preparation for lvrs, complete course of services, to include a minimum of 16 days of services Pre-op service lvrs complete
G0303 0010 3 Pre-operative pulmonary surgery services for preparation for lvrs, 10 to 15 days of services Pre-op service lvrs 10-15dos
G0304 0010 3 Pre-operative pulmonary surgery services for preparation for lvrs, 1 to 9 days of services Pre-op service lvrs 1-9 dos
G0305 0010 3 Post-discharge pulmonary surgery services after lvrs, minimum of 6 days of services Post op service lvrs min 6
G0306 0010 3 Complete cbc, automated (hgb, hct, rbc, wbc, without platelet count) and automated wbc differential count Cbc/diffwbc w/o platelet
G0307 0010 3 Complete (cbc), automated (hgb, hct, rbc, wbc; without platelet count) Cbc without platelet
G0328 0010 3 Colorectal cancer screening; fecal occult blood test, immunoassay, 1-3 simultaneous Fecal blood scrn immunoassay
G0329 0010 3 Electromagnetic therapy, to one or more areas for chronic stage iii and stage iv pressure ulcers, arterial ulcers, diabetic ulcers and venous stasis ulcers not demonstrating measurable signs of healing after 30 days of conventional care as part of a therapy plan of care Electromagntic tx for ulcers
G0333 0010 3 Pharmacy dispensing fee for inhalation drug(s); initial 30-day supply as a beneficiary Dispense fee initial 30 day
G0337 0010 3 Hospice evaluation and counseling services, pre-election Hospice evaluation preelecti
G0339 0010 3 Image-guided robotic linear accelerator-based stereotactic radiosurgery, complete course of therapy in one session or first session of fractionated treatment Robot lin-radsurg com, first
G0340 0010 3 Image-guided robotic linear accelerator-based stereotactic radiosurgery, delivery including collimator changes and custom plugging, fractionated treatment, all lesions, per session, second through fifth sessions, maximum five sessions per course of treatment Robt lin-radsurg fractx 2-5
G0341 0010 3 Percutaneous islet cell transplant, includes portal vein catheterization and infusion Percutaneous islet celltrans
G0342 0010 3 Laparoscopy for islet cell transplant, includes portal vein catheterization and infusion Laparoscopy islet cell trans
G0343 0010 3 Laparotomy for islet cell transplant, includes portal vein catheterization and infusion Laparotomy islet cell transp
G0364 0010 3 Bone marrow aspiration performed with bone marrow biopsy through the same incision on the same date of service Bone marrow aspirate &biopsy
G0365 0010 3 Vessel mapping of vessels for hemodialysis access (services for preoperative vessel mapping prior to creation of hemodialysis access using an autogenous hemodialysis conduit, including arterial inflow and venous outflow) Vessel mapping hemo access
G0372 0010 3 Physician service required to establish and document the need for a power mobility device Md service required for pmd
G0378 0010 3 Hospital observation service, per hour Hospital observation per hr
G0379 0010 3 Direct admission of patient for hospital observation care Direct refer hospital observ
G0380 0010 3 Level 1 hospital emergency department visit provided in a type b emergency department; (the ed must meet at least one of the following requirements: (1) it is licensed by the state in which it is located under applicable state law as an emergency room or emergency department; (2) it is held out to the public (by name, posted signs, advertising, or other means) as a place that provides care for emergency medical conditions on an urgent basis without requiring a previously scheduled appointment; or (3) during the calendar year immediately preceding the calendar year in which a determination under 42 cfr 489.24 is being made, based on a representative sample of patient visits that occurred during that calendar year, it provides at least one-third of all of its outpatient visits for the treatment of emergency medical conditions on an urgent basis without requiring a previously scheduled appointment) Lev 1 hosp type b ed visit
G0381 0010 3 Level 2 hospital emergency department visit provided in a type b emergency department; (the ed must meet at least one of the following requirements: (1) it is licensed by the state in which it is located under applicable state law as an emergency room or emergency department; (2) it is held out to the public (by name, posted signs, advertising, or other means) as a place that provides care for emergency medical conditions on an urgent basis without requiring a previously scheduled appointment; or (3) during the calendar year immediately preceding the calendar year in which a determination under 42 cfr 489.24 is being made, based on a representative sample of patient visits that occurred during that calendar year, it provides at least one-third of all of its outpatient visits for the treatment of emergency medical conditions on an urgent basis without requiring a previously scheduled appointment) Lev 2 hosp type b ed visit
G0382 0010 3 Level 3 hospital emergency department visit provided in a type b emergency department; (the ed must meet at least one of the following requirements: (1) it is licensed by the state in which it is located under applicable state law as an emergency room or emergency department; (2) it is held out to the public (by name, posted signs, advertising, or other means) as a place that provides care for emergency medical conditions on an urgent basis without requiring a previously scheduled appointment; or (3) during the calendar year immediately preceding the calendar year in which a determination under 42 cfr 489.24 is being made, based on a representative sample of patient visits that occurred during that calendar year, it provides at least one-third of all of its outpatient visits for the treatment of emergency medical conditions on an urgent basis without requiring a previously scheduled appointment) Lev 3 hosp type b ed visit
G0383 0010 3 Level 4 hospital emergency department visit provided in a type b emergency department; (the ed must meet at least one of the following requirements: (1) it is licensed by the state in which it is located under applicable state law as an emergency room or emergency department; (2) it is held out to the public (by name, posted signs, advertising, or other means) as a place that provides care for emergency medical conditions on an urgent basis without requiring a previously scheduled appointment; or (3) during the calendar year immediately preceding the calendar year in which a determination under 42 cfr 489.24 is being made, based on a representative sample of patient visits that occurred during that calendar year, it provides at least one-third of all of its outpatient visits for the treatment of emergency medical conditions on an urgent basis without requiring a previously scheduled appointment) Lev 4 hosp type b ed visit
G0384 0010 3 Level 5 hospital emergency department visit provided in a type b emergency department; (the ed must meet at least one of the following requirements: (1) it is licensed by the state in which it is located under applicable state law as an emergency room or emergency department; (2) it is held out to the public (by name, posted signs, advertising, or other means) as a place that provides care for emergency medical conditions on an urgent basis without requiring a previously scheduled appointment; or (3) during the calendar year immediately preceding the calendar year in which a determination under 42 cfr 489.24 is being made, based on a representative sample of patient visits that occurred during that calendar year, it provides at least one-third of all of its outpatient visits for the treatment of emergency medical conditions on an urgent basis without requiring a previously scheduled appointment) Lev 5 hosp type b ed visit
G0389 0010 3 Ultrasound b-scan and/or real time with image documentation; for abdominal aortic aneurysm (aaa) screening Ultrasound exam aaa screen
G0390 0010 3 Trauma response team associated with hospital critical care service Trauma respons w/hosp criti
G0396 0010 3 Alcohol and/or substance (other than tobacco) abuse structured assessment (e.g., audit, dast), and brief intervention 15 to 30 minutes Alcohol/subs interv 15-30mn
G0397 0010 3 Alcohol and/or substance (other than tobacco) abuse structured assessment (e.g., audit, dast), and intervention, greater than 30 minutes Alcohol/subs interv >30 min
G0398 0010 3 Home sleep study test (hst) with type ii portable monitor, unattended; minimum of 7 channels: eeg, eog, emg, ecg/heart rate, airflow, respiratory effort and oxygen saturation Home sleep test/type 2 porta
G0399 0010 3 Home sleep test (hst) with type iii portable monitor, unattended; minimum of 4 channels: 2 respiratory movement/airflow, 1 ecg/heart rate and 1 oxygen saturation Home sleep test/type 3 porta
G0400 0010 3 Home sleep test (hst) with type iv portable monitor, unattended; minimum of 3 channels Home sleep test/type 4 porta
G0402 0010 3 Initial preventive physical examination; face-to-face visit, services limited to new beneficiary during the first 12 months of medicare enrollment Initial preventive exam
G0403 0010 3 Electrocardiogram, routine ecg with 12 leads; performed as a screening for the initial preventive physical examination with interpretation and report Ekg for initial prevent exam
G0404 0010 3 Electrocardiogram, routine ecg with 12 leads; tracing only, without interpretation and report, performed as a screening for the initial preventive physical examination Ekg tracing for initial prev
G0405 0010 3 Electrocardiogram, routine ecg with 12 leads; interpretation and report only, performed as a screening for the initial preventive physical examination Ekg interpret & report preve
G0406 0010 3 Follow-up inpatient consultation, limited, physicians typically spend 15 minutes communicating with the patient via telehealth Inpt/tele follow up 15
G0407 0010 3 Follow-up inpatient consultation, intermediate, physicians typically spend 25 minutes communicating with the patient via telehealth Inpt/tele follow up 25
G0408 0010 3 Follow-up inpatient consultation, complex, physicians typically spend 35 minutes communicating with the patient via telehealth Inpt/tele follow up 35
G0409 0010 3 Social work and psychological services, directly relating to and/or furthering the patient’s rehabilitation goals, each 15 minutes, face-to-face; individual (services provided by a corf-qualified social worker or psychologist in a corf) Corf related serv 15 mins ea
G0410 0010 3 Group psychotherapy other than of a multiple-family group, in a partial hospitalization setting, approximately 45 to 50 minutes Grp psych partial hosp 45-50
G0411 0010 3 Interactive group psychotherapy, in a partial hospitalization setting, approximately 45 to 50 minutes Inter active grp psych parti
G0412 0010 3 Open treatment of iliac spine(s), tuberosity avulsion, or iliac wing fracture(s), unilateral or bilateral for pelvic bone fracture patterns which do not disrupt the pelvic ring includes internal fixation, when performed Open tx iliac spine uni/bil
G0413 0010 3 Percutaneous skeletal fixation of posterior pelvic bone fracture and/or dislocation, for fracture patterns which disrupt the pelvic ring, unilateral or bilateral, (includes ilium, sacroiliac joint and/or sacrum) Pelvic ring fracture uni/bil
G0414 0010 3 Open treatment of anterior pelvic bone fracture and/or dislocation for fracture patterns which disrupt the pelvic ring, unilateral or bilateral, includes internal fixation when performed (includes pubic symphysis and/or superior/inferior rami) Pelvic ring fx treat int fix
G0415 0010 3 Open treatment of posterior pelvic bone fracture and/or dislocation, for fracture patterns which disrupt the pelvic ring, unilateral or bilateral, includes internal fixation, when performed (includes ilium, sacroiliac joint and/or sacrum) Open tx post pelvic fxcture
G0416 0010 3 Surgical pathology, gross and microscopic examinations, for prostate needle biopsy, any method Prostate biopsy, any mthd
G0417 0010 3 Surgical pathology, gross and microscopic examination, for prostate needle biopsy, any method, 21-40 specimens Sat biopsy prostate 21-40
G0418 0010 3 Surgical pathology, gross and microscopic examination, for prostate needle biopsy, any method, 41-60 specimens Sat biopsy prostate 41-60
G0419 0010 3 Surgical pathology, gross and microscopic examination, for prostate needle biopsy, any method, >60 specimens Sat biopsy prostate: >60
G0420 0010 3 Face-to-face educational services related to the care of chronic kidney disease; individual, per session, per one hour Ed svc ckd ind per session
G0421 0010 3 Face-to-face educational services related to the care of chronic kidney disease; group, per session, per one hour Ed svc ckd grp per session
G0422 0010 3 Intensive cardiac rehabilitation; with or without continuous ecg monitoring with exercise, per session Intens cardiac rehab w/exerc
G0423 0010 3 Intensive cardiac rehabilitation; with or without continuous ecg monitoring; without exercise, per session Intens cardiac rehab no exer
G0424 0010 3 Pulmonary rehabilitation, including exercise (includes monitoring), one hour, per session, up to two sessions per day Pulmonary rehab w exer
G0425 0010 3 Telehealth consultation, emergency department or initial inpatient, typically 30 minutes communicating with the patient via telehealth Inpt/ed teleconsult30
G0426 0010 3 Telehealth consultation, emergency department or initial inpatient, typically 50 minutes communicating with the patient via telehealth Inpt/ed teleconsult50
G0427 0010 3 Telehealth consultation, emergency department or initial inpatient, typically 70 minutes or more communicating with the patient via telehealth Inpt/ed teleconsult70
G0428 0010 3 Collagen meniscus implant procedure for filling meniscal defects (e.g., cmi, collagen scaffold, menaflex) Collagen meniscus implant
G0429 0010 3 Dermal filler injection(s) for the treatment of facial lipodystrophy syndrome (lds) (e.g., as a result of highly active antiretroviral therapy) Dermal filler injection(s)
G0431 0010 3 Drug screen, qualitative; multiple drug classes by high complexity test method (e.g., immunoassay, enzyme assay), per patient encounter Drug screen multiple class
G0432 0010 3 Infectious agent antibody detection by enzyme immunoassay (eia) technique, hiv-1 and/or hiv-2, screening Eia hiv-1/hiv-2 screen
G0433 0010 3 Infectious agent antibody detection by enzyme-linked immunosorbent assay (elisa) technique, hiv-1 and/or hiv-2, screening Elisa hiv-1/hiv-2 screen
G0434 0010 3 Drug screen, other than chromatographic; any number of drug classes, by clia waived test or moderate complexity test, per patient encounter Drug screen multi drug class
G0435 0010 3 Infectious agent antibody detection by rapid antibody test, hiv-1 and/or hiv-2, screening Oral hiv-1/hiv-2 screen
G0436 0010 3 Smoking and tobacco cessation counseling visit for the asymptomatic patient; intermediate, greater than 3 minutes, up to 10 minutes Tobacco-use counsel 3-10 min
G0437 0010 3 Smoking and tobacco cessation counseling visit for the asymptomatic patient; intensive, greater than 10 minutes Tobacco-use counsel>10min
G0438 0010 3 Annual wellness visit; includes a personalized prevention plan of service (pps), initial visit Ppps, initial visit
G0439 0010 3 Annual wellness visit, includes a personalized prevention plan of service (pps), subsequent visit Ppps, subseq visit
G0442 0010 3 Annual alcohol misuse screening, 15 minutes Annual alcohol screen 15 min
G0443 0010 3 Brief face-to-face behavioral counseling for alcohol misuse, 15 minutes Brief alcohol misuse counsel
G0444 0010 3 Annual depression screening, 15 minutes Depression screen annual
G0445 0010 3 High intensity behavioral counseling to prevent sexually transmitted infection; face-to-face, individual, includes: education, skills training and guidance on how to change sexual behavior; performed semi-annually, 30 minutes High inten beh couns std 30m
G0446 0010 3 Annual, face-to-face intensive behavioral therapy for cardiovascular disease, individual, 15 minutes Intens behave ther cardio dx
G0447 0010 3 Face-to-face behavioral counseling for obesity, 15 minutes Behavior counsel obesity 15m
G0448 0010 3 Insertion or replacement of a permanent pacing cardioverter-defibrillator system with transvenous lead(s), single or dual chamber with insertion of pacing electrode, cardiac venous system, for left ventricular pacing Place perm pacing cardiovert
G0451 0010 3 Development testing, with interpretation and report, per standardized instrument form Devlopment test interpt&rep
G0452 0010 3 Molecular pathology procedure; physician interpretation and report Molecular pathology interpr
G0453 0010 3 Continuous intraoperative neurophysiology monitoring, from outside the operating room (remote or nearby), per patient, (attention directed exclusively to one patient) each 15 minutes (list in addition to primary procedure) Cont intraop neuro monitor
G0454 0010 3 Physician documentation of face-to-face visit for durable medical equipment determination performed by nurse practitioner, physician assistant or clinical nurse specialist Md document visit by npp
G0455 0010 3 Preparation with instillation of fecal microbiota by any method, including assessment of donor specimen Fecal microbiota prep instil
G0456 0010 3 Negative pressure wound therapy, (e.g. vacuum assisted drainage collection) using a mechanically-powered device, not durable medical equipment, including provision of cartridge and dressing(s), topical application(s), wound assessment, and instructions for ongoing care, per session; total wounds(s) surface area less than or equal to 50 square centimeters Neg pre wound <=50 sq cm
G0457 0010 3 Negative pressure wound therapy, (e.g. vacuum assisted drainage collection) using a mechanically-powered device, not durable medical equipment, including provision of cartridge and dressing(s), topical application(s), wound assessment, and instructions for ongoing care, per session; total wounds(s) surface area greater than 50 square centimeters Neg pres wound >50 sq cm
G0458 0010 3 Low dose rate (ldr) prostate brachytherapy services, composite rate Ldr prostate brachy comp rat
G0459 0010 3 Inpatient telehealth pharmacologic management, including prescription, use, and review of medication with no more than minimal medical psychotherapy Telehealth inpt pharm mgmt
G0460 0010 3 Autologous platelet rich plasma for chronic wounds/ulcers, including phlebotomy, centrifugation, and all other preparatory procedures, administration and dressings, per treatment Autologous prp for ulcers
G0461 0010 3 Immunohistochemistry or immunocytochemistry, per specimen; first single or multiplex antibody stain Immunohisto/cyto chem 1st st
G0462 0010 3 Immunohistochemistry or immunocytochemistry, per specimen; each additional single or multiplex antibody stain (list separately in addition to code for primary procedure) Immunohisto/cyto chem add
G0463 0010 3 Hospital outpatient clinic visit for assessment and management of a patient Hospital outpt clinic visit
G0464 0010 3 Colorectal cancer screening; stool-based dna and fecal occult hemoglobin (e.g., kras, ndrg4 and bmp3) Colorec ca scr, sto bas dna
G0466 0010 3 Federally qualified health center (fqhc) visit, new patient; a medically-necessary, face-to-face encounter (one-on-one) between a new patient and a fqhc practitioner during which time one or more fqhc services are rendered and includes a typical bundle of medicare-covered services that would be furnished per diem to a patient receiving a fqhc visit Fqhc visit new patient
G0467 0010 3 Federally qualified health center (fqhc) visit, established patient; a medically-necessary, face-to-face encounter (one-on-one) between an established patient and a fqhc practitioner during which time one or more fqhc services are rendered and includes a typical bundle of medicare-covered services that would be furnished per diem to a patient receiving a fqhc visit Fqhc visit, estab pt
G0468 0010 3 Federally qualified health center (fqhc) visit, ippe or awv; a fqhc visit that includes an initial preventive physical examination (ippe) or annual wellness visit (awv) and includes a typical bundle of medicare-covered services that would be furnished per diem to a patient receiving an ippe or awv Fqhc visit, ippe or awv
G0469 0010 3 Federally qualified health center (fqhc) visit, mental health, new patient; a medically-necessary, face-to-face mental health encounter (one-on-one) between a new patient and a fqhc practitioner during which time one or more fqhc services are rendered and includes a typical bundle of medicare-covered services that would be furnished per diem to a patient receiving a mental health visit Fqhc visit, mh new pt
G0470 0010 3 Federally qualified health center (fqhc) visit, mental health, established patient; a medically-necessary, face-to-face mental health encounter (one-on-one) between an established patient and a fqhc practitioner during which time one or more fqhc services are rendered and includes a typical bundle of medicare-covered services that would be furnished per diem to a patient receiving a mental health visit Fqhc visit, mh estab pt
G0471 0010 3 Collection of venous blood by venipuncture or urine sample by catheterization from an individual in a skilled nursing facility (snf) or by a laboratory on behalf of a home health agency (hha) Ven blood coll snf/hha
G0472 0010 3 Hepatitis c antibody screening, for individual at high risk and other covered indication(s) Hep c screen high risk/other
G0473 0010 3 Face-to-face behavioral counseling for obesity, group (2-10), 30 minutes Group behave couns 2-10
G0475 0010 3 Hiv antigen/antibody, combination assay, screening Hiv combination assay
G0476 0010 3 Infectious agent detection by nucleic acid (dna or rna); human papillomavirus (hpv), high-risk types (e.g., 16, 18, 31, 33, 35, 39, 45, 51, 52, 56, 58, 59, 68) for cervical cancer screening, must be performed in addition to pap test Hpv combo assay ca screen
G0477 0010 3 Drug test(s), presumptive, any number of drug classes; any number of devices or procedures, (e.g., immunoassay) capable of being read by direct optical observation only (e.g., dipsticks, cups, cards, cartridges), includes sample validation when performed, per date of service Drug test presump optical
G0478 0010 3 Drug test(s), presumptive, any number of drug classes; any number of devices or procedures, (e.g., immunoassay) read by instrument-assisted direct optical observation (e.g., dipsticks, cups, cards, cartridges), includes sample validation when performed, per date of service Drug test presump opt inst
G0479 0010 3 Drug test(s), presumptive, any number of drug classes; any number of devices or procedures by instrumented chemistry analyzers utilizing immunoassay, enzyme assay, tof, maldi, ldtd, desi, dart, ghpc, gc mass spectrometry), includes sample validation when performed, per date of service Drug test presump not opt
G0480 0010 3 Drug test(s), definitive, utilizing (1) drug identification methods able to identify individual drugs and distinguish between structural isomers (but not necessarily stereoisomers), including, but not limited to gc/ms (any type, single or tandem) and lc/ms (any type, single or tandem and excluding immunoassays (e.g., ia, eia, elisa, emit, fpia) and enzymatic methods (e.g., alcohol dehydrogenase)), (2) stable isotope or other universally recognized internal standards in all samples (e.g., to control for matrix effects, interferences and variations in signal strength), and (3) method or drug-specific calibration and matrix-matched quality control material (e.g., to control for instrument variations and mass spectral drift); qualitative or quantitative, all sources, includes specimen validity testing, per day; 1-7 drug class(es), including metabolite(s) if performed Drug test def 1-7 classes
G0481 0010 3 Drug test(s), definitive, utilizing (1) drug identification methods able to identify individual drugs and distinguish between structural isomers (but not necessarily stereoisomers), including, but not limited to gc/ms (any type, single or tandem) and lc/ms (any type, single or tandem and excluding immunoassays (e.g., ia, eia, elisa, emit, fpia) and enzymatic methods (e.g., alcohol dehydrogenase)), (2) stable isotope or other universally recognized internal standards in all samples (e.g., to control for matrix effects, interferences and variations in signal strength), and (3) method or drug-specific calibration and matrix-matched quality control material (e.g., to control for instrument variations and mass spectral drift); qualitative or quantitative, all sources, includes specimen validity testing, per day; 8-14 drug class(es), including metabolite(s) if performed Drug test def 8-14 classes
G0482 0010 3 Drug test(s), definitive, utilizing (1) drug identification methods able to identify individual drugs and distinguish between structural isomers (but not necessarily stereoisomers), including, but not limited to gc/ms (any type, single or tandem) and lc/ms (any type, single or tandem and excluding immunoassays (e.g., ia, eia, elisa, emit, fpia) and enzymatic methods (e.g., alcohol dehydrogenase)), (2) stable isotope or other universally recognized internal standards in all samples (e.g., to control for matrix effects, interferences and variations in signal strength), and (3) method or drug-specific calibration and matrix-matched quality control material (e.g., to control for instrument variations and mass spectral drift); qualitative or quantitative, all sources, includes specimen validity testing, per day; 15-21 drug class(es), including metabolite(s) if performed Drug test def 15-21 classes
G0483 0010 3 Drug test(s), definitive, utilizing (1) drug identification methods able to identify individual drugs and distinguish between structural isomers (but not necessarily stereoisomers), including, but not limited to gc/ms (any type, single or tandem) and lc/ms (any type, single or tandem and excluding immunoassays (e.g., ia, eia, elisa, emit, fpia) and enzymatic methods (e.g., alcohol dehydrogenase)), (2) stable isotope or other universally recognized internal standards in all samples (e.g., to control for matrix effects, interferences and variations in signal strength), and (3) method or drug-specific calibration and matrix-matched quality control material (e.g., to control for instrument variations and mass spectral drift); qualitative or quantitative, all sources, includes specimen validity testing, per day; 22 or more drug class(es), including metabolite(s) if performed Drug test def 22+ classes
G0490 0010 3 Face-to-face home health nursing visit by a rural health clinic (rhc) or federally qualified health center (fqhc) in an area with a shortage of home health agencies; (services limited to rn or lpn only) Home visit rn, lpn by rhc/fq
G0491 0010 3 Dialysis procedure at a medicare certified esrd facility for acute kidney injury without esrd Dialysis acu kidney no esrd
G0492 0010 3 Dialysis procedure with single evaluation by a physician or other qualified health care professional for acute kidney injury without esrd Md/oth eval acut kid no esrd
G0493 0010 3 Skilled services of a registered nurse (rn) for the observation and assessment of the patient’s condition, each 15 minutes (the change in the patient’s condition requires skilled nursing personnel to identify and evaluate the patient’s need for possible modification of treatment in the home health or hospice setting) Rn care ea 15 min hh/hospice
G0494 0010 3 Skilled services of a licensed practical nurse (lpn) for the observation and assessment of the patient’s condition, each 15 minutes (the change in the patient’s condition requires skilled nursing personnel to identify and evaluate the patient’s need for possible modification of treatment in the home health or hospice setting) Lpn care ea 15min hh/hospice
G0495 0010 3 Skilled services of a registered nurse (rn), in the training and/or education of a patient or family member, in the home health or hospice setting, each 15 minutes Rn care train/edu in hh
G0496 0010 3 Skilled services of a licensed practical nurse (lpn), in the training and/or education of a patient or family member, in the home health or hospice setting, each 15 minutes Lpn care train/edu in hh
G0498 0010 3 Chemotherapy administration, intravenous infusion technique; initiation of infusion in the office/clinic setting using office/clinic pump/supplies, with continuation of the infusion in the community setting (e.g., home, domiciliary, rest home or assisted living) using a portable pump provided by the office/clinic, includes follow up office/clinic visit at the conclusion of the infusion Chemo extend iv infus w/pump
G0499 0010 3 Hepatitis b screening in non-pregnant, high risk individual includes hepatitis b surface antigen (hbsag), antibodies to hbsag (anti-hbs) and antibodies to hepatitis b core antigen (anti-hbc), and is followed by a neutralizing confirmatory test, when performed, only for an initially reactive hbsag result Hepb screen high risk indiv
G0500 0010 3 Moderate sedation services provided by the same physician or other qualified health care professional performing a gastrointestinal endoscopic service that sedation supports, requiring the presence of an independent trained observer to assist in the monitoring of the patient’s level of consciousness and physiological status; initial 15 minutes of intra-service time; patient age 5 years or older (additional time may be reported with 99153, as appropriate) Mod sedat endo service >5yrs
G0501 0010 3 Resource-intensive services for patients for whom the use of specialized mobility-assistive technology (such as adjustable height chairs or tables, patient lift, and adjustable padded leg supports) is medically necessary and used during the provision of an office/outpatient, evaluation and management visit (list separately in addition to primary service) Resource-inten svc during ov
G0502 0010 3 Initial psychiatric collaborative care management, first 70 minutes in the first calendar month of behavioral health care manager activities, in consultation with a psychiatric consultant, and directed by the treating physician or other qualified health care professional, with the following required elements: outreach to and engagement in treatment of a patient directed by the treating physician or other qualified health care professional; initial assessment of the patient, including administration of validated rating scales, with the development of an individualized treatment plan; review by the psychiatric consultant with modifications of the plan if recommended; entering patient in a registry and tracking patient follow-up and progress using the registry, with appropriate documentation, and participation in weekly caseload consultation with the psychiatric consultant; and provision of brief interventions using evidence-based techniques such as behavioral activation, motivational interviewing, and other focused treatment strategies Init psych care manag, 70min
G0503 0010 3 Subsequent psychiatric collaborative care management, first 60 minutes in a subsequent month of behavioral health care manager activities, in consultation with a psychiatric consultant, and directed by the treating physician or other qualified health care professional, with the following required elements: tracking patient follow-up and progress using the registry, with appropriate documentation; participation in weekly caseload consultation with the psychiatric consultant; ongoing collaboration with and coordination of the patient’s mental health care with the treating physician or other qualified health care professional and any other treating mental health providers; additional review of progress and recommendations for changes in treatment, as indicated, including medications, based on recommendations provided by the psychiatric consultant; provision of brief interventions using evidence-based techniques such as behavioral activation, motivational interviewing, and other focused treatment strategies; monitoring of patient outcomes using validated rating scales; and relapse prevention planning with patients as they achieve remission of symptoms and/or other treatment Subseq psych care man,60mi
G0503 0020 4 goals and are prepared for discharge from active treatment  
G0504 0010 3 Initial or subsequent psychiatric collaborative care management, each additional 30 minutes in a calendar month of behavioral health care manager activities, in consultation with a psychiatric consultant, and directed by the treating physician or other qualified health care professional (list separately in addition to code for primary procedure); (use g0504 in conjunction with g0502, g0503) Init/sub psych care add 30 m
G0505 0010 3 Cognition and functional assessment using standardized instruments with development of recorded care plan for the patient with cognitive impairment, history obtained from patient and/or caregiver, in office or other outpatient setting or home or domiciliary or rest home Cog/func assessment outpt
G0506 0010 3 Comprehensive assessment of and care planning for patients requiring chronic care management services (list separately in addition to primary monthly care management service) Comp asses care plan ccm svc
G0507 0010 3 Care management services for behavioral health conditions, at least 20 minutes of clinical staff time, directed by a physician or other qualified health care professional, per calendar month, with the following required elements: initial assessment or follow-up monitoring, including the use of applicable validated rating scales; behavioral health care planning in relation to behavioral/psychiatric health problems, including revision for patients who are not progressing or whose status changes; facilitating and coordinating treatment such as psychotherapy, pharmacotherapy, counseling and/or psychiatric consultation; and continuity of care with a designated member of the care team Care manage serv minimum 20
G0508 0010 3 Telehealth consultation, critical care, initial , physicians typically spend 60 minutes communicating with the patient and providers via telehealth Crit care telehea consult 60
G0509 0010 3 Telehealth consultation, critical care, subsequent, physicians typically spend 50 minutes communicating with the patient and providers via telehealth Crit care telehea consult 50
G0511 0010 3 Rural health clinic or federally qualified health center (rhc or fqhc) only, general care management, 20 minutes or more of clinical staff time for chronic care management services or behavioral health integration services directed by an rhc or fqhc practitioner (physician, np, pa, or cnm), per calendar month Ccm/bhi by rhc/fqhc 20min mo
G0512 0010 3 Rural health clinic or federally qualified health center (rhc/fqhc) only, psychiatric collaborative care model (psychiatric cocm), 60 minutes or more of clinical staff time for psychiatric cocm services directed by an rhc or fqhc practitioner (physician, np, pa, or cnm) and including services furnished by a behavioral health care manager and consultation with a psychiatric consultant, per calendar month Cocm by rhc/fqhc 60 min mo
G0513 0010 3 Prolonged preventive service(s) (beyond the typical service time of the primary procedure), in the office or other outpatient setting requiring direct patient contact beyond the usual service; first 30 minutes (list separately in addition to code for preventive service) Prolong prev svcs, first 30m
G0514 0010 3 Prolonged preventive service(s) (beyond the typical service time of the primary procedure), in the office or other outpatient setting requiring direct patient contact beyond the usual service; each additional 30 minutes (list separately in addition to code g0513 for additional 30 minutes of preventive service) Prolong prev svcs, addl 30m
G0515 0010 3 Development of cognitive skills to improve attention, memory, problem solving (includes compensatory training), direct (one-on-one) patient contact, each 15 minutes Cognitive skills development
G0516 0010 3 Insertion of non-biodegradable drug delivery implants, 4 or more (services for subdermal rod implant) Insert drug del implant, >=4
G0517 0010 3 Removal of non-biodegradable drug delivery implants, 4 or more (services for subdermal implants) Remove drug implant
G0518 0010 3 Removal with reinsertion, non-biodegradable drug delivery implants, 4 or more (services for subdermal implants) Remove w insert drug implant
G0659 0010 3 Drug test(s), definitive, utilizing drug identification methods able to identify individual drugs and distinguish between structural isomers (but not necessarily stereoisomers), including but not limited to gc/ms (any type, single or tandem) and lc/ms (any type, single or tandem), excluding immunoassays (e.g., ia, eia, elisa, emit, fpia) and enzymatic methods (e.g., alcohol dehydrogenase), performed without method or drug-specific calibration, without matrix-matched quality control material, or without use of stable isotope or other universally recognized internal standard(s) for each drug, drug metabolite or drug class per specimen; qualitative or quantitative, all sources, includes specimen validity testing, per day, any number of drug classes Drug test def simple all cl
G0908 0010 3 Most recent hemoglobin (hgb) level > 12.0 g/dl Hgb > 12 g/dl
G0909 0010 3 Hemoglobin level measurement not documented, reason not given Hbg not doc
G0910 0010 3 Most recent hemoglobin level <= 12.0 g/dl Hgb <= 12 g/dl
G0913 0010 3 Improvement in visual function achieved within 90 days following cataract surgery Improve visual funct
G0914 0010 3 Patient care survey was not completed by patient Survey not complete
G0915 0010 3 Improvement in visual function not achieved within 90 days following cataract surgery No improve visual funct
G0916 0010 3 Satisfaction with care achieved within 90 days following cataract surgery Satisfy with care
G0917 0010 3 Patient satisfaction survey was not completed by patient Satisfy survey not complete
G0918 0010 3 Satisfaction with care not achieved within 90 days following cataract surgery No satisfy with care
G0919 0010 3 Influenza immunization ordered or recommended (to be given at alternate location or alternate provider); vaccine not available at time of visit Flu immunize not avail
G0920 0010 3 Type, anatomic location, and activity all documented Type loc act doc
G0921 0010 3 Documentation of patient reason(s) for not being able to assess (e.g., patient refuses endoscopic and/or radiologic assessment) Doc pt reas no assess
G0922 0010 3 No documentation of disease type, anatomic location, and activity, reason not given Type loc act not doc
G1000 0010 3 Clinical decision support mechanism applied pathways, as defined by the medicare appropriate use criteria program Cdsm applied pathways
G1001 0010 3 Clinical decision support mechanism evicore, as defined by the medicare appropriate use criteria program Cdsm evicore
G1002 0010 3 Clinical decision support mechanism medcurrent, as defined by the medicare appropriate use criteria program Cdsm medcurrent
G1003 0010 3 Clinical decision support mechanism medicalis, as defined by the medicare appropriate use criteria program Cdsm medicalis
G1004 0010 3 Clinical decision support mechanism national decision support company, as defined by the medicare appropriate use criteria program Cdsm ndsc
G1005 0010 3 Clinical decision support mechanism national imaging associates, as defined by the medicare appropriate use criteria program Cdsm nia
G1006 0010 3 Clinical decision support mechanism test appropriate, as defined by the medicare appropriate use criteria program Cdsm test approp
G1007 0010 3 Clinical decision support mechanism aim specialty health, as defined by the medicare appropriate use criteria program Cdsm aim
G1008 0010 3 Clinical decision support mechanism cranberry peak, as defined by the medicare appropriate use criteria program Cdsm cranberry pk
G1009 0010 3 Clinical decision support mechanism sage health management solutions, as defined by the medicare appropriate use criteria program Cdsm sage health
G1010 0010 3 Clinical decision support mechanism stanson, as defined by the medicare appropriate use criteria program Cdsm stanson
G1011 0010 3 Clinical decision support mechanism, qualified tool not otherwise specified, as defined by the medicare appropriate use criteria program Cdsm qualified nos
G2000 0010 3 Blinded administration of convulsive therapy procedure, either electroconvulsive therapy (ect, current covered gold standard) or magnetic seizure therapy (mst, non-covered experimental therapy), performed in an approved ide-based clinical trial, per treatment session Blinded conv. tx mdd clin tr
G2001 0010 3 Brief (20 minutes) in-home visit for a new patient post-discharge. for use only in a medicare-approved cmmi model. (services must be furnished within a beneficiary’s home, domiciliary, rest home, assisted living and/or nursing facility within 90 days following discharge from an inpatient facility and no more than 9 times.) Post d/c h vst new pt 20 m
G2002 0010 3 Limited (30 minutes) in-home visit for a new patient post-discharge. for use only in a medicare-approved cmmi model. (services must be furnished within a beneficiary’s home, domiciliary, rest home, assisted living and/or nursing facility within 90 days following discharge from an inpatient facility and no more than 9 times.) Post-d/c h vst new pt 30 m
G2003 0010 3 Moderate (45 minutes) in-home visit for a new patient post-discharge. for use only in a medicare-approved cmmi model. (services must be furnished within a beneficiary’s home, domiciliary, rest home, assisted living and/or nursing facility within 90 days following discharge from an inpatient facility and no more than 9 times.) Post-d/c h vst new pt 45 m
G2004 0010 3 Comprehensive (60 minutes) in-home visit for a new patient post-discharge. for use only in a medicare-approved cmmi model. (services must be furnished within a beneficiary’s home, domiciliary, rest home, assisted living and/or nursing facility within 90 days following discharge from an inpatient facility and no more than 9 times.) Post-d/c h vst new pt 60 m
G2005 0010 3 Extensive (75 minutes) in-home visit for a new patient post-discharge. for use only in a medicare-approved cmmi model. (services must be furnished within a beneficiary’s home, domiciliary, rest home, assisted living and/or nursing facility within 90 days following discharge from an inpatient facility and no more than 9 times.) Post-d/c h vst new pt 75 m
G2006 0010 3 Brief (20 minutes) in-home visit for an existing patient post-discharge. for use only in a medicare-approved cmmi model. (services must be furnished within a beneficiary’s home, domiciliary, rest home, assisted living and/or nursing facility within 90 days following discharge from an inpatient facility and no more than 9 times.) Post-d/c h vst ext pt 20 m
G2007 0010 3 Limited (30 minutes) in-home visit for an existing patient post-discharge. for use only in a medicare-approved cmmi model. (services must be furnished within a beneficiary’s home, domiciliary, rest home, assisted living and/or nursing facility within 90 days following discharge from an inpatient facility and no more than 9 times.) Post-d/c h vst ext pt 30 m
G2008 0010 3 Moderate (45 minutes) in-home visit for an existing patient post-discharge. for use only in a medicare-approved cmmi model. (services must be furnished within a beneficiary’s home, domiciliary, rest home, assisted living and/or nursing facility within 90 days following discharge from an inpatient facility and no more than 9 times.) Post-d/c h vst ext pt 45 m
G2009 0010 3 Comprehensive (60 minutes) in-home visit for an existing patient post-discharge. for use only in a medicare-approved cmmi model. (services must be furnished within a beneficiary’s home, domiciliary, rest home, assisted living and/or nursing facility within 90 days following discharge from an inpatient facility and no more than 9 times.) Post-d/c h vst ext pt 60 m
G2010 0010 3 Remote evaluation of recorded video and/or images submitted by an established patient (e.g., store and forward), including interpretation with follow-up with the patient within 24 business hours, not originating from a related e/m service provided within the previous 7 days nor leading to an e/m service or procedure within the next 24 hours or soonest available appointment Remot image submit by pt
G2011 0010 3 Alcohol and/or substance (other than tobacco) abuse structured assessment (e.g., audit, dast), and brief intervention, 5-14 minutes Alcohol/sub abuse assess
G2012 0010 3 Brief communication technology-based service, e.g. virtual check-in, by a physician or other qualified health care professional who can report evaluation and management services, provided to an established patient, not originating from a related e/m service provided within the previous 7 days nor leading to an e/m service or procedure within the next 24 hours or soonest available appointment; 5-10 minutes of medical discussion Brief check in by md/qhp
G2013 0010 3 Extensive (75 minutes) in-home visit for an existing patient post-discharge. for use only in a medicare-approved cmmi model. (services must be furnished within a beneficiary’s home, domiciliary, rest home, assisted living and/or nursing facility within 90 days following discharge from an inpatient facility and no more than 9 times.) Post-d/c h vst ext pt 75 m
G2014 0010 3 Limited (30 minutes) care plan oversight. for use only in a medicare-approved cmmi model. (services must be furnished within a beneficiary’s home, domiciliary, rest home, assisted living and/or nursing facility within 90 days following discharge from an inpatient facility and no more than 9 times.) Post-d/c care plan overs 30m
G2015 0010 3 Comprehensive (60 mins) home care plan oversight. for use only in a medicare-approved cmmi model. (services must be furnished within a beneficiary’s home, domiciliary, rest home, assisted living and/or nursing facility within 90 days following discharge from an inpatient facility.) Post-d/c care plan overs 60m
G2021 0010 3 Health care practitioners rendering treatment in place (tip) Hea care pract tx in place
G2022 0010 3 A model participant (ambulance supplier/provider), the beneficiary refuses services covered under the model (transport to an alternate destination/treatment in place) Benef refuses service, mod
G2058 0010 3 Chronic care management services, each additional 20 minutes of clinical staff time directed by a physician or other qualified health care professional, per calendar month (list separately in addition to code for primary procedure). (do not report g2058 for care management services of less than 20 minutes additional to the first 20 minutes of chronic care management services during a calendar month). (use g2058 in conjunction with 99490). (do not report 99490, g2058 in the same calendar month as 99487, 99489, 99491)). Ccm add 20min
G2061 0010 3 Qualified nonphysician healthcare professional online assessment, for an established patient, for up to seven days, cumulative time during the 7 days; 5-10 minutes Qual nonmd est pt 5-10m
G2062 0010 3 Qualified nonphysician healthcare professional online assessment service, for an established patient, for up to seven days, cumulative time during the 7 days; 11-20 minutes Qual nonmd est pt 11-20m
G2063 0010 3 Qualified nonphysician qualified healthcare professional assessment service, for an established patient, for up to seven days, cumulative time during the 7 days; 21 or more minutes Qual nonmd est pt 21>min
G2064 0010 3 Comprehensive care management services for a single high-risk disease, e.g., principal care management, at least 30 minutes of physician or other qualified health care professional time per calendar month with the following elements: one complex chronic condition lasting at least 3 months, which is the focus of the care plan, the condition is of sufficient severity to place patient at risk of hospitalization or have been the cause of a recent hospitalization, the condition requires development or revision of disease-specific care plan, the condition requires frequent adjustments in the medication regimen, and/or the management of the condition is unusually complex due to comorbidities Md mang high risk dx 30
G2065 0010 3 Comprehensive care management for a single high-risk disease services, e.g. principal care management, at least 30 minutes of clinical staff time directed by a physician or other qualified health care professional, per calendar month with the following elements: one complex chronic condition lasting at least 3 months, which is the focus of the care plan, the condition is of sufficient severity to place patient at risk of hospitalization or have been cause of a recent hospitalization, the condition requires development or revision of disease-specific care plan, the condition requires frequent adjustments in the medication regimen, and/or the management of the condition is unusually complex due to comorbidities Clin mang h risk dx 30
G2066 0010 3 Interrogation device evaluation(s), (remote) up to 30 days; implantable cardiovascular physiologic monitor system, implantable loop recorder system, or subcutaneous cardiac rhythm monitor system, remote data acquisition(s), receipt of transmissions and technician review, technical support and distribution of results Inter devc remote 30d
G2067 0010 3 Medication assisted treatment, methadone; weekly bundle including dispensing and/or administration, substance use counseling, individual and group therapy, and toxicology testing, if performed (provision of the services by a medicare-enrolled opioid treatment program) Med assist tx meth wk
G2068 0010 3 Medication assisted treatment, buprenorphine (oral); weekly bundle including dispensing and/or administration, substance use counseling, individual and group therapy, and toxicology testing if performed (provision of the services by a medicare-enrolled opioid treatment program) Med assist tx bupre oral
G2069 0010 3 Medication assisted treatment, buprenorphine (injectable); weekly bundle including dispensing and/or administration, substance use counseling, individual and group therapy, and toxicology testing if performed (provision of the services by a medicare-enrolled opioid treatment program) Med assist tx inject
G2070 0010 3 Medication assisted treatment, buprenorphine (implant insertion); weekly bundle including dispensing and/or administration, substance use counseling, individual and group therapy, and toxicology testing if performed (provision of the services by a medicare-enrolled opioid treatment program) Med assist tx implant
G2071 0010 3 Medication assisted treatment, buprenorphine (implant removal); weekly bundle including dispensing and/or administration, substance use counseling, individual and group therapy, and toxicology testing if performed (provision of the services by a medicare-enrolled opioid treatment program) Med tx remove implant
G2072 0010 3 Medication assisted treatment, buprenorphine (implant insertion and removal); weekly bundle including dispensing and/or administration, substance use counseling, individual and group therapy, and toxicology testing if performed (provision of the services by a medicare-enrolled opioid treatment program) Med tx insert/remove imp
G2073 0010 3 Medication assisted treatment, naltrexone; weekly bundle including dispensing and/or administration, substance use counseling, individual and group therapy, and toxicology testing if performed (provision of the services by a medicare-enrolled opioid treatment program) Med tx naltrexone
G2074 0010 3 Medication assisted treatment, weekly bundle not including the drug, including substance use counseling, individual and group therapy, and toxicology testing if performed (provision of the services by a medicare-enrolled opioid treatment program) Med assist tx no drug
G2075 0010 3 Medication assisted treatment, medication not otherwise specified; weekly bundle including dispensing and/or administration, substance use counseling, individual and group therapy, and toxicology testing, if performed (provision of the services by a medicare-enrolled opioid treatment program) Med tx meds nos
G2076 0010 3 Intake activities, including initial medical examination that is a complete, fully documented physical evaluation and initial assessment by a program physician or a primary care physician, or an authorized healthcare professional under the supervision of a program physician qualified personnel that includes preparation of a treatment plan that includes the patient’s short-term goals and the tasks the patient must perform to complete the short-term goals; the patient’s requirements for education, vocational rehabilitation, and employment; and the medical, psycho- social, economic, legal, or other supportive services that a patient needs, conducted by qualified personnel (provision of the services by a medicare-enrolled opioid treatment program); list separately in addition to code for primary procedure Intake act w/med exam
G2077 0010 3 Periodic assessment; assessing periodically by qualified personnel to determine the most appropriate combination of services and treatment (provision of the services by a medicare-enrolled opioid treatment program); list separately in addition to code for primary procedure Periodic assessment
G2078 0010 3 Take-home supply of methadone; up to 7 additional day supply (provision of the services by a medicare-enrolled opioid treatment program); list separately in addition to code for primary procedure Take-home meth
G2079 0010 3 Take-home supply of buprenorphine (oral); up to 7 additional day supply (provision of the services by a medicare-enrolled opioid treatment program); list separately in addition to code for primary procedure Take-hom buprenorphine
G2080 0010 3 Each additional 30 minutes of counseling in a week of medication assisted treatment, (provision of the services by a medicare-enrolled opioid treatment program); list separately in addition to code for primary procedure Add 30 mins counsel
G2081 0010 3 Patients age 66 and older in institutional special needs plans (snp) or residing in long-term care with a pos code 32, 33, 34, 54 or 56 for more than 90 days during the measurement period Pt 66+ snp or ltc pos > 90d
G2082 0010 3 Office or other outpatient visit for the evaluation and management of an established patient that requires the supervision of a physician or other qualified health care professional and provision of up to 56 mg of esketamine nasal self-administration, includes 2 hours post-administration observation Visit esketamine 56m or less
G2083 0010 3 Office or other outpatient visit for the evaluation and management of an established patient that requires the supervision of a physician or other qualified health care professional and provision of greater than 56 mg esketamine nasal self-administration, includes 2 hours post-administration observation Visit esketamine, > 56m
G2086 0010 3 Office-based treatment for opioid use disorder, including development of the treatment plan, care coordination, individual therapy and group therapy and counseling; at least 70 minutes in the first calendar month Off base opioid tx 70min
G2087 0010 3 Office-based treatment for opioid use disorder, including care coordination, individual therapy and group therapy and counseling; at least 60 minutes in a subsequent calendar month Off base opioid tx, 60 m
G2088 0010 3 Office-based treatment for opioid use disorder, including care coordination, individual therapy and group therapy and counseling; each additional 30 minutes beyond the first 120 minutes (list separately in addition to code for primary procedure) Off base opioid tx, add30
G2089 0010 3 Most recent hemoglobin a1c (hba1c) level 7.0 to 9.0% A1c level 7 to 9%
G2090 0010 3 Patients 66 years of age and older with at least one claim/encounter for frailty during the measurement period and a dispensed medication for dementia during the measurement period or the year prior to the measurement period Pt 66+ frailty and med dem
G2091 0010 3 Patients 66 years of age and older with at least one claim/encounter for frailty during the measurement period and either one acute inpatient encounter with a diagnosis of advanced illness or two outpatient, observation, ed or nonacute inpatient encounters on different dates of service with an advanced illness diagnosis during the measurement period or the year prior to the measurement period Pt 66+ frailty and adv ill
G2092 0010 3 Angiotensin converting enzyme (ace) inhibitor or angiotensin receptor blocker (arb) or angiotensin receptor-neprilysin inhibitor (arni) therapy prescribed or currently being taken Ace arb arni
G2093 0010 3 Documentation of medical reason(s) for not prescribing ace inhibitor or arb or arni therapy (e.g., hypotensive patients who are at immediate risk of cardiogenic shock, hospitalized patients who have experienced marked azotemia, allergy, intolerance, other medical reasons) Med doc rsn no ace arn arni
G2094 0010 3 Documentation of patient reason(s) for not prescribing ace inhibitor or arb or arni therapy (e.g., patient declined, other patient reasons) Pt rsn no ace arn arni
G2095 0010 3 Documentation of system reason(s) for not prescribing ace inhibitor or arb or arni therapy (e.g., other system reasons) Sys rsn no ace arn arni
G2096 0010 3 Angiotensin converting enzyme (ace) inhibitor or angiotensin receptor blocker (arb) or angiotensin receptor-neprilysin inhibitor (arni) therapy was not prescribed, reason not given No rsn ace arb arni
G2097 0010 3 Children with a competing diagnosis for upper respiratory infection within three days of diagnosis of pharyngitis (e.g., intestinal infection, pertussis, bacterial infection, lyme disease, otitis media, acute sinusitis, acute pharyngitis, acute tonsillitis, chronic sinusitis, infection of the pharynx/larynx/tonsils/adenoids, prostatitis, cellulitis, mastoiditis, or bone infections, acute lymphadenitis, impetigo, skin staph infections, pneumonia/gonococcal infections, venereal disease (syphilis, chlamydia, inflammatory diseases [female reproductive organs]), infections of the kidney, cystitis or uti Child dx uri 3d of other dx
G2098 0010 3 Patients 66 years of age and older with at least one claim/encounter for frailty during the measurement period and a dispensed medication for dementia during the measurement period or the year prior to the measurement period Pt 66+ frailty and med dem
G2099 0010 3 Patients 66 years of age and older with at least one claim/encounter for frailty during the measurement period and either one acute inpatient encounter with a diagnosis of advanced illness or two outpatient, observation, ed or nonacute inpatient encounters on different dates of service with an advanced illness diagnosis during the measurement period or the year prior to the measurement period Pt 66+ frailty and adv ill
G2100 0010 3 Patients 66 years of age and older with at least one claim/encounter for frailty during the measurement period and a dispensed medication for dementia during the measurement period or the year prior to the measurement period Pt 66+ frailty and med dem
G2101 0010 3 Patients 66 years of age and older with at least one claim/encounter for frailty during the measurement period and either one acute inpatient encounter with a diagnosis of advanced illness or two outpatient, observation, ed or nonacute inpatient encounters on different dates of service with an advanced illness diagnosis during the measurement period or the year prior to the measurement period Pt 66+ frailty and adv ill
G2102 0010 3 Dilated retinal eye exam with interpretation by an ophthalmologist or optometrist documented and reviewed Dil retinal eye exam
G2103 0010 3 Seven standard field stereoscopic photos with interpretation by an ophthalmologist or optometrist documented and reviewed 7 stereo photos interpret
G2104 0010 3 Eye imaging validated to match diagnosis from seven standard field stereoscopic photos results documented and reviewed Eye img valid w/7 stereo
G2105 0010 3 Patients age 66 or older in institutional special needs plans (snp) or residing in long-term care with pos code 32, 33, 34, 54 or 56 for more than 90 days during the measurement period Pt 66+ lt ints > 90
G2106 0010 3 Patients 66 years of age and older with at least one claim/encounter for frailty during the measurement period and a dispensed medication for dementia during the measurement period or the year prior to the measurement period Pt 66+ lt ints > 90
G2107 0010 3 Patients 66 years of age and older with at least one claim/encounter for frailty during the measurement period and either one acute inpatient encounter with a diagnosis of advanced illness or two outpatient, observation, ed or nonacute inpatient encounters on different dates of service with an advanced illness diagnosis during the measurement period or the year prior to the measurement period Pt 66+ frailty and adv ill
G2108 0010 3 Patients age 66 or older in institutional special needs plans (snp) or residing in long-term care with pos code 32, 33, 34, 54 or 56 for more than 90 days during the measurement period Pt 66+ lt ints > 90
G2109 0010 3 Patients 66 years of age and older with at least one claim/encounter for frailty during the measurement period and a dispensed medication for dementia during the measurement period or the year prior to the measurement period Pt 66+ frailty and med dem
G2110 0010 3 Patients 66 years of age and older with at least one claim/encounter for frailty during the measurement period and either one acute inpatient encounter with a diagnosis of advanced illness or two outpatient, observation, ed or nonacute inpatient encounters on different dates of service with an advanced illness diagnosis during the measurement period or the year prior to the measurement period Pt 66+ frailty and adv ill
G2112 0010 3 Patient receiving <=5 mg daily prednisone (or equivalent), or ra activity is worsening, or glucocorticoid use is for less than 6 months Pred<=5 mg ra glu <6m
G2113 0010 3 Patient receiving >5 mg daily prednisone (or equivalent) for longer than 6 months, and improvement or no change in disease activity Pred>5 mg >6m, no chg da
G2114 0010 3 Patients 66-80 years of age with at least one claim/encounter for frailty during the measurement period and a dispensed medication for dementia during the measurement period or the year prior to the measurement period Pt 66-80 frailty and med dem
G2115 0010 3 Patients 66 years of age and older with at least one claim/encounter for frailty during the measurement period and a dispensed medication for dementia during the measurement period or the year prior to the measurement period Pt 66+ frailty and med dem
G2116 0010 3 Patients 66 years of age and older with at least one claim/encounter for frailty during the measurement period and either one acute inpatient encounter with a diagnosis of advanced illness or two outpatient, observation, ed or nonacute inpatient encounters on different dates of service with an advanced illness diagnosis during the measurement period or the year prior to the measurement period Pt 66+ frailty and adv ill
G2117 0010 3 Patients 66-80 years of age with at least one claim/encounter for frailty during the measurement period and either one acute inpatient encounter with a diagnosis of advanced illness or two outpatient, observation, ed or nonacute inpatient encounters on different dates of service with an advanced illness diagnosis during the measurement period or the year prior to the measurement period Pt 66-80 frailty and adv ill
G2118 0010 3 Patients 81 years of age and older with a evidence of frailty during the measurement period Pt 81+ frailty
G2119 0010 3 Within the past 2 years, calcium and/or vitamin d optimization has been ordered or performed Calc vitd opt
G2120 0010 3 Within the past 2 years, calcium and/or vitamin d optimization has not been ordered or performed No calc vitd opt
G2121 0010 3 Psychosis, depression, anxiety, apathy, and impulse control disorder assessed Psy dep anx ap and icd asse
G2122 0010 3 Psychosis, depression, anxiety, apathy, and impulse control disorder not assessed Psy/dep/anx/apandicd noasse
G2123 0010 3 Patients 66-80 years of age and had at least one claim/encounter for frailty during the measurement period and either one acute inpatient encounter with a diagnosis of advanced illness or two outpatient, observation, ed or nonacute inpatient encounters on different dates of service with an advanced illness diagnosis during the measurement period or the year prior to the measurement period Pt 66-80 frailty med dem
G2124 0010 3 Patients 66-80 years of age and had at least one claim/encounter for frailty during the measurement period and a dispensed dementia medication Pt 66-80 frailty adv ill
G2125 0010 3 Patients 81 years of age and older with evidence of frailty during the measurement period Pt 81+ frailty
G2126 0010 3 Patients 66 years of age or older and had at least one claim/encounter for frailty during the measurement period and either one acute inpatient encounter with a diagnosis of advanced illness or two outpatient, observation, ed or nonacute inpatient encounters on different dates of service with an advanced illness diagnosis during the measurement period or the year prior to the measurement period Pt 66+ frailty adv ill
G2127 0010 3 Patients 66 years of age or older and had at least one claim/encounter for frailty during the measurement period and a dispensed dementia medication Pt 66+ frailty med dem
G2128 0010 3 Documentation of medical reason(s) for not on a daily aspirin or other antiplatelet (e.g. history of gastrointestinal bleed, intra-cranial bleed, blood disorders, idiopathic thrombocytopenic purpura (itp), gastric bypass or documentation of active anticoagulant use during the measurement period) No aspirin med rsn
G2129 0010 3 Procedure-related bp’s not taken during an outpatient visit. examples include same day surgery, ambulatory service center, g.i. lab, dialysis, infusion center, chemotherapy No bp outpt
G2130 0010 3 Patients age 66 or older in institutional special needs plans (snp) or residing in long-term care with pos code 32, 33, 34, 54 or 56 for more than 90 days during the measurement period Pt 66+ lt inst > 90
G2131 0010 3 Patients 81 years and older with a diagnosis of frailty Pt 81+ frailty
G2132 0010 3 Patients 66-80 years of age with at least one claim/encounter for frailty during the measurement period and a dispensed medication for dementia during the measurement period or the year prior to the measurement period Pt 66-80 frailty and med dem
G2133 0010 3 Patients 66-80 years of age with at least one claim/encounter for frailty during the measurement period and either one acute inpatient encounter with a diagnosis of advanced illness or two outpatient, observation, ed or nonacute inpatient encounters on different dates of service with an advanced illness diagnosis during the measurement period or the year prior to the measurement period Pt 66-80 frailty and adv ill
G2134 0010 3 Patients 66 years of age or older with at least one claim/encounter for frailty during the measurement period and a dispensed medication for dementia during the measurement period or the year prior to the measurement period Pt 66+ frailty and med dem
G2135 0010 3 Patients 66 years of age or older with at least one claim/encounter for frailty during the measurement period and either one acute inpatient encounter with a diagnosis of advanced illness or two outpatient, observation, ed or nonacute inpatient encounters on different dates of service with an advanced illness diagnosis during the measurement period or the year prior to the measurement period Pt 66+ frailty and adv ill
G2136 0010 3 Back pain measured by the visual analog scale (vas) at three months (6 ? 20 weeks) postoperatively was less than or equal to 3.0 or back pain measured by the visual analog scale (vas) within three months preoperatively and at three months (6 ? 20 weeks) postoperatively demonstrated an improvement of 5.0 points or greater Bk pain vas 6-20wk = 3
G2137 0010 3 Back pain measured by the visual analog scale (vas) at three months (6 ? 20 weeks) postoperatively was greater than 3.0 and back pain measured by the visual analog scale (vas) within three months preoperatively and at three months (6 ? 20 weeks) postoperatively demonstrated a change of less than an improvement of 5.0 points Bk pain vas 6-20wk > 3
G2138 0010 3 Back pain as measured by the visual analog scale (vas) at one year (9 to 15 months) postoperatively was less than or equal to 3.0 or back pain measured by the visual analog scale (vas) within three months preoperatively and at one year (9 to 15 months) postoperatively demonstrated a change of 5.0 points or greater Bk pain vas 9-15mo = 3
G2139 0010 3 Back pain measured by the visual analog scale (vas) pain at one year (9 to 15 months) postoperatively was greater than 3.0 and back pain measured by the visual analog scale (vas) within three months preoperatively and at one year (9 to 15 months) postoperatively demonstrated a change of less than 5.0 Bk pain vas 9-20mo > 3
G2140 0010 3 Leg pain measured by the visual analog scale (vas) at three months (6 ? 20 weeks) postoperatively was less than or equal to 3.0 or leg pain measured by the visual analog scale (vas) within three months preoperatively and at three months (6 - 20 weeks) postoperatively demonstrated an improvement of 5.0 points or greater Leg pain vas 6-20wk = 3
G2141 0010 3 Leg pain measured by the visual analog scale (vas) at three months (6 ? 20 weeks) postoperatively was greater than 3.0 and leg pain measured by the visual analog scale (vas) within three months preoperatively and at three months (6 - 20 weeks) postoperatively demonstrated less than an improvement of 5.0 points Leg pain vas 6-20wk > 3
G2142 0010 3 Functional status measured by the oswestry disability index (odi version 2.1a) at one year (9 to 15 months) postoperatively was less than or equal to 22 or functional status measured by the odi version 2.1a within three months preoperatively and at one year (9 to 15 months) postoperatively demonstrated a change of 30 points or greater Fs odi 9-15mo postop<= 22
G2143 0010 3 Functional status measured by the oswestry disability index (odi version 2.1a) at one year (9 to 15 months) postoperatively was greater than 22 and functional status measured by the odi version 2.1a within three months preoperatively and at one year (9 to 15 months) postoperatively demonstrated a change of less than 30 points Fs odi 9-15mo > 22
G2144 0010 3 Functional status measured by the oswestry disability index (odi version 2.1a) at three months (6 ? 20 weeks) postoperatively was less than or equal to 22 or functional status measured by the odi version 2.1a within three months preoperatively and at three months (6 - 20 weeks) postoperatively demonstrated a change of 30 points or greater Fs odi 6-20wk postop > 22
G2145 0010 3 Functional status measured by the oswestry disability index (odi version 2.1a) at three months (6 ? 20 weeks) postoperatively was greater than 22 and functional status measured by the odi version 2.1a within three months preoperatively and at three months (6 - 20 weeks) postoperatively demonstrated a change of less than 30 points Fsodi 6-20wk >22 or chg 30pt
G2146 0010 3 Leg pain as measured by the visual analog scale (vas) at one year (9 to 15 months) postoperatively was less than or equal to 3.0 or leg pain measured by the visual analog scale (vas) within three months preoperatively and at one year (9 to 15 months) postoperatively demonstrated an improvement of 5.0 points or greater Leg pain vas 9-15mo <= 3
G2147 0010 3 Leg pain measured by the visual analog scale (vas) at one year (9 to 15 months) postoperatively was greater than 3.0 and leg pain measured by the visual analog scale (vas) within three months preoperatively and at one year (9 to 15 months) postoperatively demonstrated less than an improvement of 5.0 points Leg pain vas 9-15mo > 3
G2148 0010 3 Performance met: multimodal pain management was used Mpm used
G2149 0010 3 Documentation of medical reason(s) for not using multimodal pain management (e.g., allergy to multiple classes of analgesics, intubated patient, hepatic failure, patient reports no pain during pacu stay, other medical reason(s)) No mpm med rsn
G2150 0010 3 Performance not met: multimodal pain management was not used No mpm
G2151 0010 3 Patients with diagnosis of a degenerative neurological condition such as als, ms, parkinson’s diagnosed at any time before or during the episode of care Dx degen neuro
G2152 0010 3 Performance met: the residual change score is equal to or greater than 0 Res change sc =0
G2153 0010 3 In hospice or using hospice services during the measurement period Hosp dur meas pd
G2154 0010 3 Patient received at least one td vaccine or one tdap vaccine between nine years prior to the start of the measurement period and the end of the measurement period Td 9 yrs start end meas
G2155 0010 3 Patient had history of at least one of the following contraindications any time during or before the measurement period: anaphylaxis due to tdap vaccine, anaphylaxis due to td vaccine or its components; encephalopathy due to tdap or td vaccination (post tetanus vaccination encephalitis, post diphtheria vaccination encephalitis or post pertussis vaccination encephalitis.) Hist contraindications
G2156 0010 3 Patient did not receive at least one td vaccine or one tdap vaccine between nine years prior to the start of the measurement period and the end of the measurement period; or have history of at least one of the following contraindications any time during or before the measurement period: anaphylaxis due to tdap vaccine, anaphylaxis due to td vaccine or its components; encephalopathy due to tdap or td vaccination (post tetanus vaccination encephalitis, post diphtheria vaccination encephalitis or post pertussis vaccination encephalitis.) No prior td or hx contra
G2157 0010 3 Patients received both the 13-valent pneumococcal conjugate vaccine and the 23-valent pneumococcal polysaccharide vaccine at least 12 months apart, with the first occurrence after the age of 60 before or during the measurement period Pneum vacc 12 mo 60+
G2158 0010 3 Patient had prior pneumococcal vaccine adverse reaction any time during or before the measurement period Pneum vacc adv rx
G2159 0010 3 Patient did not receive both the 13-valent pneumococcal conjugate vaccine and the 23-valent pneumococcal polysaccharide vaccine at least 12 months apart, with the first occurrence after the age of 60 before or during measurement period; or have prior pneumococcal vaccine adverse reaction any time during or before the measurement period No pneum vacc 12 mo 60+
G2160 0010 3 Patient received at least one dose of the herpes zoster live vaccine or two doses of the herpes zoster recombinant vaccine (at least 28 days apart) anytime on or after the patient’s 50th birthday before or during the measurement period Herpzos 50+
G2161 0010 3 Patient had prior adverse reaction caused by zoster vaccine or its components any time during or before the measurement period Adv rx zos
G2162 0010 3 Patient did not receive at least one dose of the herpes zoster live vaccine or two doses of the herpes zoster recombinant vaccine (at least 28 days apart) anytime on or after the patient’s 50th birthday before or during the measurement period; or have prior adverse reaction caused by zoster vaccine or its components any time during or before the measurement period No herpzos 50+
G2163 0010 3 Patient received an influenza vaccine on or between july 1 of the year prior to the measurement period and june 30 of the measurement period Infl vacc 07/01 to 06/30
G2164 0010 3 Patient had a prior influenza virus vaccine adverse reaction any time before or during the measurement period Adv rx infl vacc
G2165 0010 3 Patient did not receive an influenza vaccine on or between july 1 of the year prior to the measurement period and june 30 of the measurement period; or did not have a prior influenza virus vaccine adverse reaction any time before or during the measurement period No infl vacc 07/01 to 06/30
G2166 0010 3 Patient refused to participate at admission and/or discharge; patient unable to complete the neck fs prom at admission or discharge due to cognitive deficit, visual deficit, motor deficit, language barrier, or low reading level, and a suitable proxy/recorder is not available; patient self-discharged early; medical reason No pt adm dx no neck fs prom
G2167 0010 3 Performance not met: the residual change score is less than 0 Res change sc < 0
G3001 0010 3 Administration and supply of tositumomab, 450 mg Admin + supply, tositumomab
G6001 0010 3 Ultrasonic guidance for placement of radiation therapy fields Echo guidance radiotherapy
G6002 0010 3 Stereoscopic x-ray guidance for localization of target volume for the delivery of radiation therapy Stereoscopic x-ray guidance
G6003 0010 3 Radiation treatment delivery, single treatment area,single port or parallel opposed ports, simple blocks or no blocks: up to 5 mev Radiation treatment delivery
G6004 0010 3 Radiation treatment delivery, single treatment area,single port or parallel opposed ports, simple blocks or no blocks: 6-10 mev Radiation treatment delivery
G6005 0010 3 Radiation treatment delivery, single treatment area,single port or parallel opposed ports, simple blocks or no blocks: 11-19 mev Radiation treatment delivery
G6006 0010 3 Radiation treatment delivery, single treatment area,single port or parallel opposed ports, simple blocks or no blocks: 20 mev or greater Radiation treatment delivery
G6007 0010 3 Radiation treatment delivery, 2 separate treatment areas, 3 or more ports on a single treatment area, use of multiple blocks: up to 5 mev Radiation treatment delivery
G6008 0010 3 Radiation treatment delivery, 2 separate treatment areas, 3 or more ports on a single treatment area, use of multiple blocks: 6-10 mev Radiation treatment delivery
G6009 0010 3 Radiation treatment delivery, 2 separate treatment areas, 3 or more ports on a single treatment area, use of multiple blocks: 11-19 mev Radiation treatment delivery
G6010 0010 3 Radiation treatment delivery, 2 separate treatment areas, 3 or more ports on a single treatment area, use of multiple blocks: 20 mev or greater Radiation treatment delivery
G6011 0010 3 Radiation treatment delivery,3 or more separate treatment areas, custom blocking, tangential ports, wedges, rotational beam, compensators, electron beam; up to 5 mev Radiation treatment delivery
G6012 0010 3 Radiation treatment delivery,3 or more separate treatment areas, custom blocking, tangential ports, wedges, rotational beam, compensators, electron beam; 6-10 mev Radiation treatment delivery
G6013 0010 3 Radiation treatment delivery,3 or more separate treatment areas, custom blocking, tangential ports, wedges, rotational beam, compensators, electron beam; 11-19 mev Radiation treatment delivery
G6014 0010 3 Radiation treatment delivery,3 or more separate treatment areas, custom blocking, tangential ports, wedges, rotational beam, compensators, electron beam; 20 mev or greater Radiation treatment delivery
G6015 0010 3 Intensity modulated treatment delivery, single or multiple fields/arcs,via narrow spatially and temporally modulated beams, binary, dynamic mlc, per treatment session Radiation tx delivery imrt
G6016 0010 3 Compensator-based beam modulation treatment delivery of inverse planned treatment using 3 or more high resolution (milled or cast) compensator, convergent beam modulated fields, per treatment session Delivery comp imrt
G6017 0010 3 Intra-fraction localization and tracking of target or patient motion during delivery of radiation therapy (eg,3d positional tracking, gating, 3d surface tracking), each fraction of treatment Intrafraction track motion
G6018 0010 3 Ileoscopy, through stoma; with transendoscopic stent placement (includes predilation) Ileoscopy w/stent
G6019 0010 3 Colonoscopy through stoma; with ablation of tumor(s), polyp(s), or other lesion(s) not amenable to removal by hot biopsy forceps, bipolar cautery or snare technique Colonoscopy lesion removal
G6020 0010 3 Colonoscopy through stoma; with transendoscopic stent placement (includes predilation) Colonoscopy w/stent
G6021 0010 3 Unlisted procedure, intestine Unlisted px small intestine
G6022 0010 3 Sigmoidoscopy, flexible; with ablation of tumor(s), polyp(s), or other lesions(s) not amenable to removal by hot biopsy forceps, bipolar cautery or snare technique Sigmoidoscopy w/ablate tumr
G6023 0010 3 Sigmoidoscopy, flexible; with transendoscopic stent placement (includes predilation) Sigmoidoscopy w/stent
G6024 0010 3 Colonoscopy, flexible; proximal to splenic flexure; with ablation of tumor(s), polyp(s), or other lesion(s) not amenable to removal by hot biopsy forceps, bipolar cautery or snare technique Lesion removal colonoscopy
G6025 0010 3 Colonoscopy, flexible, proximal to splenic flexure; with transendoscopic stent placement (includes predilation) Colonoscopy w/stent
G6027 0010 3 Anoscopy, high resolution (hra) (with magnification and chemical agent enhancement); diagnostic, including collection of specimen(s) by brushing or washing when performed Anoscopy hra w/spec collect
G6028 0010 3 Anoscopy, high resolution (hra) (with magnification and chemical agent enhancement); with biopsy(ies) Anoscopy hra w/biopsy
G6030 0010 3 Amitriptyline Assay of amitriptyline
G6031 0010 3 Benzodiazepines Assay of benzodiazepines
G6032 0010 3 Desipramine Assay of desipramine
G6034 0010 3 Doxepin Assay of doxepin
G6035 0010 3 Gold Assay of gold
G6036 0010 3 Assay of imipramine Assay of imipramine
G6037 0010 3 Nortriptyline Assay of nortiptyline
G6038 0010 3 Salicylate Assay of salicylate
G6039 0010 3 Acetaminophen Assay of acetaminophen
G6040 0010 3 Alcohol (ethanol); any specimen except breath Assay of ethanol
G6041 0010 3 Alkaloids, urine, quantitative Assay of urine alkaloids
G6042 0010 3 Amphetamine or methamphetamine Assay of amphetamines
G6043 0010 3 Barbiturates, not elsewhere specified Assay of barbiturates
G6044 0010 3 Cocaine or metabolite Assay of cocaine
G6045 0010 3 Dihydrocodeinone Assay of dihydrocodeinone
G6046 0010 3 Dihydromorphinone Assay of dihydromorphinone
G6047 0010 3 Dihydrotestosterone Assay of dihydrotestosterone
G6048 0010 3 Dimethadione Assay of dimethadione
G6049 0010 3 Epiandrosterone Asssay of epiandrosterone
G6050 0010 3 Ethchlorvynol Assay of ethchlorvynol
G6051 0010 3 Flurazepam Assay of flurazepam
G6052 0010 3 Meprobamate Assay of meprobamate
G6053 0010 3 Methadone Assay of methadone
G6054 0010 3 Methsuximide Assay of methsuximide
G6055 0010 3 Nicotine Assay of nicotine
G6056 0010 3 Opiate(s), drug and metabolites, each procedure Assay of opiates
G6057 0010 3 Phenothiazine Assay of phenothiazine
G6058 0010 3 Drug confirmation, each procedure Drug confirmation
G8126 0010 3 Patient with a diagnosis of major depression documented as being treated with antidepressant medication during the entire 84 day (12 week) acute treatment phase Pt treat w/antidepress12wks
G8127 0010 3 Patient with a diagnosis of major depression not documented as being treated with antidepressant medication during the entire 84 day (12 week) acute treatment phase Pt not treat w/antidepres12w
G8128 0010 3 Clinician documented that patient was not an eligible candidate for antidepressant medication during the entire 12 week acute treatment phase measure Pt inelig for antidepres med
G8395 0010 3 Left ventricular ejection fraction (lvef) >= 40% or documentation as normal or mildly depressed left ventricular systolic function Lvef>=40% doc normal or mild
G8396 0010 3 Left ventricular ejection fraction (lvef) not performed or documented Lvef not performed
G8397 0010 3 Dilated macular or fundus exam performed, including documentation of the presence or absence of macular edema and level of severity of retinopathy Dil macula/fundus exam/w doc
G8398 0010 3 Dilated macular or fundus exam not performed Dil macular/fundus not perfo
G8399 0010 3 Patient with documented results of a central dual-energy x-ray absorptiometry (dxa) ever being performed Pt w/dxa results document
G8400 0010 3 Patient with central dual-energy x-ray absorptiometry (dxa) results not documented, reason not given Pt w/dxa no results doc
G8401 0010 3 Clinician documented that patient was not an eligible candidate for screening Pt inelig osteo screen measu
G8404 0010 3 Lower extremity neurological exam performed and documented Low extemity neur exam docum
G8405 0010 3 Lower extremity neurological exam not performed Low extemity neur not perfor
G8406 0010 3 Clinician documented that patient was not an eligible candidate for lower extremity neurological exam measure Pt inelig lower extrem neuro
G8410 0010 3 Footwear evaluation performed and documented Eval on foot documented
G8415 0010 3 Footwear evaluation was not performed Eval on foot not performed
G8416 0010 3 Clinician documented that patient was not an eligible candidate for footwear evaluation measure Pt inelig footwear evaluatio
G8417 0010 3 Bmi is documented above normal parameters and a follow-up plan is documented Calc bmi abv up param f/u
G8418 0010 3 Bmi is documented below normal parameters and a follow-up plan is documented Calc bmi blw low param f/u
G8419 0010 3 Bmi documented outside normal parameters, no follow-up plan documented, no reason given Calc bmi out nrm param nof/u
G8420 0010 3 Bmi is documented within normal parameters and no follow-up plan is required Calc bmi norm parameters
G8421 0010 3 Bmi not documented and no reason is given Bmi not calculated
G8422 0010 3 Bmi not documented, documentation the patient is not eligible for bmi calculation Pt inelig bmi calculation
G8427 0010 3 Eligible clinician attests to documenting in the medical record they obtained, updated, or reviewed the patient’s current medications Docrev cur meds by elig clin
G8428 0010 3 Current list of medications not documented as obtained, updated, or reviewed by the eligible clinician, reason not given Cur meds not document
G8430 0010 3 Eligible clinician attests to documenting in the medical record the patient is not eligible for a current list of medications being obtained, updated, or reviewed by the eligible clinician Ec at doc medrec pt not elig
G8431 0010 3 Screening for depression is documented as being positive and a follow-up plan is documented Pos clin depres scrn f/u doc
G8432 0010 3 Depression screening not documented, reason not given Dep scr not doc, rng
G8433 0010 3 Screening for depression not completed, documented reason Scr for dep not cpt doc rsn
G8442 0010 3 Pain assessment not documented as being performed, documentation the patient is not eligible for a pain assessment using a standardized tool at the time of the encounter Doc pain as nt perf, not elg
G8450 0010 3 Beta-blocker therapy prescribed Beta-bloc rx pt w/abn lvef
G8451 0010 3 Beta-blocker therapy for lvef < 40% not prescribed for reasons documented by the clinician (e.g., low blood pressure, fluid overload, asthma, patients recently treated with an intravenous positive inotropic agent, allergy, intolerance, other medical reasons, patient declined, other patient reasons, or other reasons attributable to the healthcare system) Pt w/abn lvef inelig b-bloc
G8452 0010 3 Beta-blocker therapy not prescribed Pt w/abn lvef b-bloc no rx
G8458 0010 3 Clinician documented that patient is not an eligible candidate for genotype testing; patient not receiving antiviral treatment for hepatitis c during the measurement period (e.g. genotype test done prior to the reporting period, patient declines, patient not a candidate for antiviral treatment) Pt inelig geno no antvir tx
G8460 0010 3 Clinician documented that patient is not an eligible candidate for quantitative rna testing at week 12; patient not receiving antiviral treatment for hepatitis c Pt inelig rna no antvir tx
G8461 0010 3 Patient receiving antiviral treatment for hepatitis c during the measurement period Pt rec antivir treat hep c
G8464 0010 3 Clinician documented that prostate cancer patient is not an eligible candidate for adjuvant hormonal therapy; low or intermediate risk of recurrence or risk of recurrence not determined Pt inelig; lo to no dter rsk
G8465 0010 3 High or very high risk of recurrence of prostate cancer High risk recurrence pro ca
G8473 0010 3 Angiotensin converting enzyme (ace) inhibitor or angiotensin receptor blocker (arb) therapy prescribed Ace/arb thxpy rx’d
G8474 0010 3 Angiotensin converting enzyme (ace) inhibitor or angiotensin receptor blocker (arb) therapy not prescribed for reasons documented by the clinician (e.g., allergy, intolerance, pregnancy, renal failure due to ace inhibitor, diseases of the aortic or mitral valve, other medical reasons) or (e.g., patient declined, other patient reasons) or (e.g., lack of drug availability, other reasons attributable to the health care system) Ace/arb not rx’d; doc reas
G8475 0010 3 Angiotensin converting enzyme (ace) inhibitor or angiotensin receptor blocker (arb) therapy not prescribed, reason not given Ace/arb thxpy not rx’d
G8476 0010 3 Most recent blood pressure has a systolic measurement of < 140 mmhg and a diastolic measurement of < 90 mmhg Bp sys <140 and dias <90
G8477 0010 3 Most recent blood pressure has a systolic measurement of >= 140 mmhg and/or a diastolic measurement of >= 90 mmhg Bp sys>=140 and/or dias >=90
G8478 0010 3 Blood pressure measurement not performed or documented, reason not given Bp not performed/doc
G8482 0010 3 Influenza immunization administered or previously received Flu immunize order/admin
G8483 0010 3 Influenza immunization was not administered for reasons documented by clinician (e.g., patient allergy or other medical reasons, patient declined or other patient reasons, vaccine not available or other system reasons) Flu imm no admin doc rea
G8484 0010 3 Influenza immunization was not administered, reason not given Flu immunize no admin
G8485 0010 3 I intend to report the diabetes mellitus (dm) measures group Report, diabetes measures
G8486 0010 3 I intend to report the preventive care measures group Report, prev care measures
G8487 0010 3 I intend to report the chronic kidney disease (ckd) measures group Report ckd measures
G8489 0010 3 I intend to report the coronary artery disease (cad) measures group Cad measures grp
G8490 0010 3 I intend to report the rheumatoid arthritis (ra) measures group Ra measures grp
G8491 0010 3 I intend to report the hiv/aids measures group Hiv/aids measures grp
G8492 0010 3 I intend to report the perioperative care measures group Periop care measures grp
G8493 0010 3 I intend to report the back pain measures group Back pain measures grp
G8494 0010 3 All quality actions for the applicable measures in the diabetes mellitus (dm) measures group have been performed for this patient Dm meas qual act perform
G8495 0010 3 All quality actions for the applicable measures in the chronic kidney disease (ckd) measures group have been performed for this patient Ckd meas qual act perform
G8496 0010 3 All quality actions for the applicable measures in the preventive care measures group have been performed for this patient Prev care mg qual act perfrm
G8497 0010 3 All quality actions for the applicable measures in the coronary artery bypass graft (cabg) measures group have been performed for this patient Cabg meas qual act perform
G8498 0010 3 All quality actions for the applicable measures in the coronary artery disease (cad) measures group have been performed for this patient Cad meas qual act perform
G8499 0010 3 All quality actions for the applicable measures in the rheumatoid arthritis (ra) measures group have been performed for this patient Ra meas qual act perform
G8500 0010 3 All quality actions for the applicable measures in the hiv/aids measures group have been performed for this patient Hiv meas qual act perform
G8501 0010 3 All quality actions for the applicable measures in the perioperative care measures group have been performed for this patient Perio meas qual act perform
G8502 0010 3 All quality actions for the applicable measures in the back pain measures group have been performed for this patient Back pain mg qual act perfrm
G8506 0010 3 Patient receiving angiotensin converting enzyme (ace) inhibitor or angiotensin receptor blocker (arb) therapy Pt rec ace/arb
G8509 0010 3 Pain assessment documented as positive using a standardized tool, follow-up plan not documented, reason not given Pos pain assess no f/u doc
G8510 0010 3 Screening for depression is documented as negative, a follow-up plan is not required Scr dep neg, no plan reqd
G8511 0010 3 Screening for depression documented as positive, follow-up plan not documented, reason not given Scr dep pos, no plan doc rng
G8530 0010 3 Autogenous av fistula received Auto av fistula recd
G8531 0010 3 Clinician documented that patient was not an eligible candidate for autogenous av fistula Pt inelig; auto av fistula
G8532 0010 3 Clinician documented that patient received vascular access other than autogenous av fistula, reason not given No auto av fistula; no reas
G8535 0010 3 Elder maltreatment screen not documented; documentation that patient is not eligible for the elder maltreatment screen at the time of the encounter Eld maltreatment not doc
G8536 0010 3 No documentation of an elder maltreatment screen, reason not given No doc elder mal scrn
G8539 0010 3 Functional outcome assessment documented as positive using a standardized tool and a care plan based on identified deficiencies on the date of functional outcome assessment, is documented Doc funct and care plan
G8540 0010 3 Functional outcome assessment not documented as being performed, documentation the patient is not eligible for a functional outcome assessment using a standardized tool at the time of the encounter Foa not doc as being perf
G8541 0010 3 Functional outcome assessment using a standardized tool not documented, reason not given No doc cur funct assess
G8542 0010 3 Functional outcome assessment using a standardized tool is documented; no functional deficiencies identified, care plan not required Doc funct no deficiencies
G8543 0010 3 Documentation of a positive functional outcome assessment using a standardized tool; care plan not documented, reason not given Cur funct asses; no care pln
G8544 0010 3 I intend to report the coronary artery bypass graft (cabg) measures group Cabg measures grp
G8545 0010 3 I intend to report the hepatitis c measures group Hepc measures grp
G8547 0010 3 I intend to report the ischemic vascular disease (ivd) measures group Ivd measures grp
G8548 0010 3 I intend to report the heart failure (hf) measures group Hf measures grp
G8549 0010 3 All quality actions for the applicable measures in the hepatitis c measures group have been performed for this patient Hepc mg qual act perform
G8551 0010 3 All quality actions for the applicable measures in the heart failure (hf) measures group have been performed for this patient Hf mg qual act perform
G8552 0010 3 All quality actions for the applicable measures in the ischemic vascular disease (ivd) measures group have been performed for this patient Ivd mg qual act perform
G8559 0010 3 Patient referred to a physician (preferably a physician with training in disorders of the ear) for an otologic evaluation Pt ref doc oto eval
G8560 0010 3 Patient has a history of active drainage from the ear within the previous 90 days Pt hx act drain prev 90 days
G8561 0010 3 Patient is not eligible for the referral for otologic evaluation for patients with a history of active drainage measure Pt inelig for ref oto eval
G8562 0010 3 Patient does not have a history of active drainage from the ear within the previous 90 days Pt no hx act drain 90 d
G8563 0010 3 Patient not referred to a physician (preferably a physician with training in disorders of the ear) for an otologic evaluation, reason not given Pt no ref oto reas no spec
G8564 0010 3 Patient was referred to a physician (preferably a physician with training in disorders of the ear) for an otologic evaluation, reason not specified) Pt ref oto eval
G8565 0010 3 Verification and documentation of sudden or rapidly progressive hearing loss Ver doc hear loss
G8566 0010 3 Patient is not eligible for the “referral for otologic evaluation for sudden or rapidly progressive hearing loss” measure Pt inelig ref oto eval
G8567 0010 3 Patient does not have verification and documentation of sudden or rapidly progressive hearing loss Pt no doc hear loss
G8568 0010 3 Patient was not referred to a physician (preferably a physician with training in disorders of the ear) for an otologic evaluation, reason not given Pt no ref otolo no spec
G8569 0010 3 Prolonged postoperative intubation (> 24 hrs) required Prol intubation req
G8570 0010 3 Prolonged postoperative intubation (> 24 hrs) not required No prol intub req
G8571 0010 3 Development of deep sternal wound infection/mediastinitis within 30 days postoperatively Ster wd ifx 30 d postop
G8572 0010 3 No deep sternal wound infection/mediastinitis No ster wd ifx
G8573 0010 3 Stroke following isolated cabg surgery Stk cabg
G8574 0010 3 No stroke following isolated cabg surgery No strk cabg
G8575 0010 3 Developed postoperative renal failure or required dialysis Postop ren fail
G8576 0010 3 No postoperative renal failure/dialysis not required No postop ren fail
G8577 0010 3 Re-exploration required due to mediastinal bleeding with or without tamponade, graft occlusion, valve dysfunction or other cardiac reason Reop req bld grft oth
G8578 0010 3 Re-exploration not required due to mediastinal bleeding with or without tamponade, graft occlusion, valve dysfunction or other cardiac reason No reop req bld grft oth
G8579 0010 3 Antiplatelet medication at discharge Antplt med disch
G8580 0010 3 Antiplatelet medication contraindicated Antplt med contraind
G8581 0010 3 No antiplatelet medication at discharge No antplt med disch
G8582 0010 3 Beta-blocker at discharge Bblock disch
G8583 0010 3 Beta-blocker contraindicated Bblock contraind
G8584 0010 3 No beta-blocker at discharge No bblock disch
G8585 0010 3 Anti-lipid treatment at discharge Antilipid treat disch
G8586 0010 3 Anti-lipid treatment contraindicated Antlip disch contra
G8587 0010 3 No anti-lipid treatment at discharge No antlipid treat disch
G8593 0010 3 Lipid profile results documented and reviewed (must include total cholesterol, hdl-c, triglycerides and calculated ldl-c) Lipid pn results
G8594 0010 3 Lipid profile not performed, reason not given No lipid prof perf
G8595 0010 3 Most recent ldl-c < 100 mg/dl Ldl < 100
G8597 0010 3 Most recent ldl-c >= 100 mg/dl Ldl >= 100
G8598 0010 3 Aspirin or another antiplatelet therapy used Asa/antiplat ther used
G8599 0010 3 Aspirin or another antiplatelet therapy not used, reason not given No asa/antiplat ther use rng
G8600 0010 3 Iv t-pa initiated within three hours (<= 180 minutes) of time last known well Tpa initi w/in 3 hrs
G8601 0010 3 Iv t-pa not initiated within three hours (<= 180 minutes) of time last known well for reasons documented by clinician No elig tpa init w/in 3 hrs
G8602 0010 3 Iv t-pa not initiated within three hours (<= 180 minutes) of time last known well, reason not given No tpa init w/in 3 hrs
G8627 0010 3 Surgical procedure performed within 30 days following cataract surgery for major complications (e.g., retained nuclear fragments, endophthalmitis, dislocated or wrong power iol, retinal detachment, or wound dehiscence) Surg proc w/in 30 days
G8628 0010 3 Surgical procedure not performed within 30 days following cataract surgery for major complications (e.g., retained nuclear fragments, endophthalmitis, dislocated or wrong power iol, retinal detachment, or wound dehiscence) No surg proc w/in 30 days
G8629 0010 3 Documentation of order for prophylactic parenteral antibiotic to be given within one hour (if fluoroquinolone or vancomycin, two hours) prior to surgical incision (or start of procedure when no incision is required) Doc antibio order b/4 surg
G8630 0010 3 Documentation that administration of prophylactic parenteral antibiotics was initiated within one hour (if fluoroquinolone or vancomycin, two hours) prior to surgical incision (or start of procedure when no incision is required), as ordered Doc antibio given b/4 surg
G8631 0010 3 Clinician documented that patient was not an eligible candidate for ordering prophylactic parenteral antibiotics to be given within one hour (if fluoroquinolone or vancomycin, two hours) prior to surgical incision (or start of procedure when no incision is required) Pt no elg 4 order antbi give
G8632 0010 3 Prophylactic parenteral antibiotics were not ordered to be given or given within one hour (if fluoroquinolone or vancomycin, two hours) prior to the surgical incision (or start of procedure when no incision is required), reason not given Doc no antibi order b/4 surg
G8633 0010 3 Pharmacologic therapy (other than minierals/vitamins) for osteoporosis prescribed Pharm ther osteo rx
G8634 0010 3 Clinician documented patient not an eligible candidate to receive pharmacologic therapy for osteoporosis Pt no elg phar ther osteo
G8635 0010 3 Pharmacologic therapy for osteoporosis was not prescribed, reason not given No pharm ther osteo rx
G8645 0010 3 I intend to report the asthma measures group Asthma measures grp
G8646 0010 3 All quality actions for the applicable measures in the asthma measures group have been performed for this patient Asthma mg qual act perform
G8647 0010 3 Risk-adjusted functional status change residual score for the knee impairment successfully calculated and the score was equal to zero (0) or greater than zero (> 0) Rafscrs ki scor >= 0
G8648 0010 3 Risk-adjusted functional status change residual score for the knee impairment successfully calculated and the score was less than zero (< 0) Rafscrs ki scor < 0
G8649 0010 3 Risk-adjusted functional status change residual score for the knee impairment not measured because the patient did not complete the fs status survey near discharge, patient not appropriate Rafscrs ki no scor
G8650 0010 3 Risk-adjusted functional status change residual score for the knee impairment not measured because the patient did not complete the knee fs prom at initial evaluation and/or near discharge, reason not given Rafs crs ki no scor no surv
G8651 0010 3 Risk-adjusted functional status change residual score for the hip impairment successfully calculated and the score was equal to zero (0) or greater than zero (> 0) Rafscrs hi scor >=0
G8652 0010 3 Risk-adjusted functional status change residual score for the hip impairment successfully calculated and the score was less than zero (< 0) Rafscrs hi scor < 0
G8653 0010 3 Risk-adjusted functional status change residual scores for the hip impairment not measured because the patient did not complete the fs status survey near discharge, patient not appropriate Rafscrs hi no scor
G8654 0010 3 Risk-adjusted functional status change residual score for the hip impairment not measured because the patient did not complete the fs intake survey on admission and/or follow up fs status survey near discharge, reason not given Rafs crs hi no scor no surv
G8655 0010 3 Risk-adjusted functional status change residual score for the lower leg, foot or ankle impairment successfully calculated and the score was equal to zero (0) or greater than zero ( > 0) Rafscrs llfai scor >= 0
G8656 0010 3 Risk-adjusted functional status change residual score for the lower leg, foot or ankle impairment successfully calculated and the score was less than zero (< 0) Rafscrs llfai scor < 0
G8657 0010 3 Risk-adjusted functional status change residual score for the lower leg, foot or ankle impairment not measured because the patient did not complete the fs status survey near discharge, patient not appropriate Rafscrs llfai no scor
G8658 0010 3 Risk-adjusted functional status change residual score for the lower leg, foot or ankle impairment not measured because the patient did not complete the fs intake survey on admission and/or follow up fs status survey near discharge, reason not given Rafscrs llfai no scor + surv
G8659 0010 3 Risk-adjusted functional status change residual score for the low back impairment successfully calculated and the score was equal to zero (0) or greater than zero (> 0) Rafscrs lbi scor >= 0
G8660 0010 3 Risk-adjusted functional status change residual score for the low back impairment successfully calculated and the score was less than zero (< 0) Rafscrs lbi scor < 0
G8661 0010 3 Risk-adjusted functional status change residual score for the low back impairment not measured because the patient did not complete the fs status survey near discharge, patient not appropriate Rafscrs lbi no scor
G8662 0010 3 Risk-adjusted functional status change residual score for the low back impairment not measured because the patient did not complete the low back fs prom at initial evaluation and/or near discharge, reason not given Rafs crs lbi no scor no surv
G8663 0010 3 Risk-adjusted functional status change residual score for the shoulder impairment successfully calculated and the score was equal to zero (0) or greater than zero (> 0) Rafscrs si scor >= 0
G8664 0010 3 Risk-adjusted functional status change residual score for the shoulder impairment successfully calculated and the score was less than zero (< 0) Rafscrs si scor < 0
G8665 0010 3 Risk-adjusted functional status change residual score for the shoulder impairment not measured because the patient did not complete the fs status survey near discharge, patient not appropriate Rafscrs si no scor
G8666 0010 3 Risk-adjusted functional status change residual score for the shoulder impairment not measured because the patient did not complete the shoulder fs prom at initial evaluation and/or near discharge, reason not given Rafs crs si no scor no surv
G8667 0010 3 Risk-adjusted functional status change residual score for the elbow, wrist or hand impairment successfully calculated and the score was equal to zero (0) or greater than zero (> 0) Rafscrs ewh scor >= 0
G8668 0010 3 Risk-adjusted functional status change residual score for the elbow, wrist or hand impairment successfully calculated and the score was less than zero (< 0) Rafscrs ewh scor < 0
G8669 0010 3 Risk-adjusted functional status change residual score for the elbow, wrist or hand impairment not measured because the patient did not complete the fs status survey near discharge, patient not appropriate Rafscrs
G8670 0010 3 Risk-adjusted functional status change residual score for the elbow, wrist or hand impairment not measured because the patient did not complete the elbow/wrist/hand fs prom at initial evaluation and/or near discharge, reason not given Rafs crs ewh no scor no surv
G8671 0010 3 Risk-adjusted functional status change residual score for the neck, cranium, mandible, thoracic spine, ribs or other general orthopedic impairment successfully calculated and the score was equal to zero (0) or greater than zero (> 0) Rafscrs goi scor >= 0
G8672 0010 3 Risk-adjusted functional status change residual score for the neck, cranium, mandible, thoracic spine, ribs or other general orthopedic impairment successfully calculated and the score was less than zero (< 0) Rafscrs goi scor < 0
G8673 0010 3 Risk-adjusted functional status change residual score for the neck, cranium, mandible, thoracic spine, ribs or other general orthopedic impairment not measured because the patient did not complete the fs status survey near discharge, patient not appropriate Rafscrs goi no scor
G8674 0010 3 Risk-adjusted functional status change residual score for the neck, cranium, mandible, thoracic spine, ribs or other general orthopedic impairment not measured because the patient did not complete the general orthopedic fs prom at initial evaluation and/or near discharge, reason not given Rafscrs neck, no msr/no foto
G8682 0010 3 Lvf testing documented as being performed prior to discharge or in the previous 12 months Lvg test perf
G8683 0010 3 Lvf testing not performed prior to discharge or in the previous 12 months for a medical or patient documented reason Pt not elig for lvf test
G8685 0010 3 Lvf testing not documented as being performed prior to discharge or in the previous 12 months, reason not given Lvf test not perf
G8694 0010 3 Left ventricular ejection fraction (lvef) < 40% Lvef <40%
G8696 0010 3 Antithrombotic therapy prescribed at discharge Antithromb thx presc
G8697 0010 3 Antithrombotic therapy not prescribed for documented reasons (e.g., patient had stroke during hospital stay, patient expired during inpatient stay, other medical reason(s)); (e.g., patient left against medical advice, other patient reason(s)) Antithromb no presc doc reas
G8698 0010 3 Antithrombotic therapy was not prescribed at discharge, reason not given Antithromb no presc no reas
G8699 0010 3 Rehabilitation services (occupational, physical or speech) ordered at or prior to discharge Rehab ordered disch
G8700 0010 3 Rehabilitation services (occupational, physical or speech) not indicated at or prior to discharge Rehab not indicated disch
G8701 0010 3 Rehabilitation services were not ordered, reason not otherwise specified Rehab not ordered
G8702 0010 3 Documentation that prophylactic antibiotics were given within 4 hours prior to surgical incision or intraoperatively Antiobiotics 4 hr prior surg
G8703 0010 3 Documentation that prophylactic antibiotics were neither given within 4 hours prior to surgical incision nor intraoperatively Antibiotics not prior surg
G8704 0010 3 12-lead electrocardiogram (ecg) performed Ecg performed
G8705 0010 3 Documentation of medical reason(s) for not performing a 12-lead electrocardiogram (ecg) Med reas no ecg
G8706 0010 3 Documentation of patient reason(s) for not performing a 12-lead electrocardiogram (ecg) Pt reas no ecg
G8707 0010 3 12-lead electrocardiogram (ecg) not performed, reason not given Ecg not performed
G8708 0010 3 Patient not prescribed or dispensed antibiotic Antibiotic not pres
G8709 0010 3 Patient prescribed or dispensed antibiotic for documented medical reason(s) within three days after the initial diagnosis of uri (e.g., intestinal infection, pertussis, bacterial infection, lyme disease, otitis media, acute sinusitis, acute pharyngitis, acute tonsillitis, chronic sinusitis, infection of the pharynx/larynx/tonsils/adenoids, prostatitis, cellulitis, mastoiditis, or bone infections, acute lymphadenitis, impetigo, skin staph infections, pneumonia/gonococcal infections, venereal disease (syphilis, chlamydia, inflammatory diseases (female reproductive organs)), infections of the kidney, cystitis or uti, and acne) Pt presc doc med rsn id uri
G8710 0010 3 Patient prescribed or dispensed antibiotic Pt pres antibiotic
G8711 0010 3 Prescribed or dispensed antibiotic Pres antibiotic
G8712 0010 3 Antibiotic not prescribed or dispensed Not pres antibiotic
G8713 0010 3 Spkt/v greater than or equal to 1.2 (single-pool clearance of urea [kt] / volume [v]) Spkt/v great 1.2 kt/v
G8714 0010 3 Hemodialysis treatment performed exactly three times per week for > 90 days Hemodialysis 3 times week
G8717 0010 3 Spkt/v less than 1.2 (single-pool clearance of urea [kt] / volume [v]), reason not given Less 1.2 kt/v
G8718 0010 3 Total kt/v greater than or equal to 1.7 per week (total clearance of urea [kt] / volume [v]) Great 1.7 kt/v per week
G8720 0010 3 Total kt/v less than 1.7 per week (total clearance of urea [kt] / volume [v]) Less 1.7 kt/v per week
G8721 0010 3 Pt category (primary tumor), pn category (regional lymph nodes), and histologic grade were documented in pathology report Pt, pn, hist grade doc
G8722 0010 3 Documentation of medical reason(s) for not including the pt category, the pn category or the histologic grade in the pathology report (e.g., re-excision without residual tumor; non-carcinomasanal canal) Med reas pt, pn, not doc
G8723 0010 3 Specimen site is other than anatomic location of primary tumor Spec sit not prim tumor
G8724 0010 3 Pt category, pn category and histologic grade were not documented in the pathology report, reason not given Pt, pn, hist grade not doc
G8725 0010 3 Fasting lipid profile performed (triglycerides, ldl-c, hdl-c and total cholesterol) Lipid profile perf doc
G8726 0010 3 Clinician has documented reason for not performing fasting lipid profile (e.g., patient declined, other patient reasons) Doc reas no lipid profile
G8728 0010 3 Fasting lipid profile not performed, reason not given Lipid profile not perf
G8730 0010 3 Pain assessment documented as positive using a standardized tool and a follow-up plan is documented Pain doc pos and plan
G8731 0010 3 Pain assessment using a standardized tool is documented as negative, no follow-up plan required Pain neg no plan
G8732 0010 3 No documentation of pain assessment, reason not given No doc of pain
G8733 0010 3 Elder maltreatment screen documented as positive and a follow-up plan is documented Doc pos elder mal scrn plan
G8734 0010 3 Elder maltreatment screen documented as negative, no follow-up required Doc neg elder mal no plan
G8735 0010 3 Elder maltreatment screen documented as positive, follow-up plan not documented, reason not given Eld mal scrn pos no plan
G8736 0010 3 Most current ldl-c <100mg/dl Ldl-c <100mg/dl
G8737 0010 3 Most current ldl-c >=100mg/dl Ldl-c >=100mg/dl
G8738 0010 3 Left ventricular ejection fraction (lvef) < 40% or documentation of severely or moderately depressed left ventricular systolic function Lvef < 40%
G8739 0010 3 Left ventricular ejection fraction (lvef) >= 40% or documentation as normal or mildly depressed left ventricular systolic function Lvef >= 40%
G8740 0010 3 Left ventricular ejection fraction (lvef) not performed or assessed, reason not given Lvef not perfrmd
G8749 0010 3 Absence of signs of melanoma (tenderness, jaundice, localized neurologic signs such as weakness, or any other sign suggesting systemic spread) or absence of symptoms of melanoma (cough, dyspnea, pain, paresthesia, or any other symptom suggesting the possibility of systemic spread of melanoma) No signs melanoma
G8751 0010 3 Smoking status and exposure to second hand smoke in the home not assessed, reason not given Smkg status not assess
G8752 0010 3 Most recent systolic blood pressure < 140 mmhg Sys bp less 140
G8753 0010 3 Most recent systolic blood pressure >= 140 mmhg Sys bp > or = 140
G8754 0010 3 Most recent diastolic blood pressure < 90 mmhg Dias bp less 90
G8755 0010 3 Most recent diastolic blood pressure >= 90 mmhg Dias bp > or = 90
G8756 0010 3 No documentation of blood pressure measurement, reason not given No bp measure doc
G8757 0010 3 All quality actions for the applicable measures in the chronic obstructive pulmonary disease (copd) measures group have been performed for this patient Copd mg qual act perform
G8758 0010 3 All quality actions for the applicable measures in the inflammatory bowel disease (ibd) measures group have been performed for this patient Ibd mg qual act perform
G8759 0010 3 All quality actions for the applicable measures in the sleep apnea measures group have been performed for this patient Osa mg qual act perform
G8761 0010 3 All quality actions for the applicable measures in the dementia measures group have been performed for this patient Dementia mg qual act perform
G8762 0010 3 All quality actions for the applicable measures in the parkinson’s disease measures group have been performed for this patient Pd mg qual act perform
G8763 0010 3 All quality actions for the applicable measures in the hypertension (htn) measures group have been performed for this patient Hyperten mg qual act perform
G8764 0010 3 All quality actions for the applicable measures in the cardiovascular prevention measures group have bee performed for this patient Car prev mg qual act perform
G8765 0010 3 All quality actions for the applicable measures in the cataract measures group have been performed for this patient Cataract mg qual act perform
G8767 0010 3 Lipid panel results documented and reviewed (must include total cholesterol, hdl-c, triglycerides and calculated ldl-c) Lipid panel res doc rev
G8768 0010 3 Documentation of medical reason(s) for not performing lipid profile (e.g., patients with palliative goals or for whom treatment of hypertension with standard treatment goals is not clinically appropriate) Doc med reas no lipid profle
G8769 0010 3 Lipid profile not performed, reason not given Lipid profile not perform
G8770 0010 3 Urine protein test result documented and reviewed Urine protein test doc rev
G8771 0010 3 Documentation of diagnosis of chronic kidney disease Doc dx ckd
G8772 0010 3 Documentation of medical reason(s) for not performing urine protein test (e.g., patients with palliative goals or for whom treatment of hypertension with standard treatment goals is not cllinically appropriate) Doc med reas no urine protn
G8773 0010 3 Urine protein test was not performed, reason not given No urine protein test
G8774 0010 3 Serum creatinine test result documented and reviewed Serum creatinine doc rev
G8775 0010 3 Documentation of medical reason(s) for not performing serum creatinine test (e.g., patients with palliative goals or for whom treatment of hypertension with standard treatment goals is not clinically appropriate) Doc med reas no serum crtn
G8776 0010 3 Serum creatinine test not performed, reason not given No serum creatinine test
G8777 0010 3 Diabetes screening test performed Diabetes screen
G8778 0010 3 Documentation of medical reason(s) for not performing diabetes screening test (e.g., patients with a diagnosis of diabetes, or with palliative goals or for whom treatment of hypertension with standard treatment goals is not clinically appropriate) Doc med reas no diabete scrn
G8779 0010 3 Diabetes screening test not performed, reason not given No diabetes screen
G8780 0010 3 Counseling for diet and physical activity performed Counsel diet phys activity
G8781 0010 3 Documentation of medical reason(s) for patient not receiving counseling for diet and physical activity (e.g., patients with palliative goals or for whom treatment of hypertension with standard treatment goals is not clinically appropriate) Doc med reas no counsel diet
G8782 0010 3 Counseling for diet and physical activity not performed, reason not given No counsel diet phys act
G8783 0010 3 Normal blood pressure reading documented, follow-up not required Bp scrn perf rec interval
G8784 0010 3 Patient not eligible (e.g., documentation the patient is not eligible due to active diagnosis of hypertension, patient refuses, urgent or emergent situation) Pt no elig for bp assess
G8785 0010 3 Blood pressure reading not documented, reason not given Bp scrn no perf at interval
G8797 0010 3 Specimen site other than anatomic location of esophagus Specimen site not esophagus
G8798 0010 3 Specimen site other than anatomic location of prostate Specimen site not prostate
G8806 0010 3 Performance of trans-abdominal or trans-vaginal ultrasound and pregnancy location documented Perf ultrsnd to lct preg doc
G8807 0010 3 Trans-abdominal or trans-vaginal ultrasound not performed for reasons documented by clinician (e.g., patient has visited the ed multiple times within 72 hours, patient has a documented intrauterine pregnancy [iup]) No ta tv ultrasnd
G8808 0010 3 Trans-abdominal or trans-vaginal ultrasound not performed, reason not given Ultrasound not perf, rng
G8809 0010 3 Rh-immunoglobulin (rhogam) ordered Rh-immunoglobulin order
G8810 0010 3 Rh-immunoglobulin (rhogam) not ordered for reasons documented by clinician (e.g., patient had prior documented receipt of rhogam within 12 weeks, patient refusal) Doc reas no rh-immuno
G8811 0010 3 Documentation rh-immunoglobulin (rhogam) was not ordered, reason not given No rh-immunoglobulin order
G8815 0010 3 Documented reason in the medical records for why the statin therapy was not prescribed (i.e., lower extremity bypass was for a patient with non-artherosclerotic disease) Doc reas no statin therapy
G8816 0010 3 Statin medication prescribed at discharge Statin med pres at disch
G8817 0010 3 Statin therapy not prescribed at discharge, reason not given Doc reas no statin med disch
G8818 0010 3 Patient discharge to home no later than post-operative day #7 Pt disch to home by day#7
G8825 0010 3 Patient not discharged to home by post-operative day #7 Pt not disch to home day#7
G8826 0010 3 Patient discharge to home no later than post-operative day #2 following evar Pt disch home day #2 evar
G8833 0010 3 Patient not discharged to home by post-operative day #2 following evar Pt not disch home day#2 evar
G8834 0010 3 Patient discharged to home no later than post-operative day #2 following cea Pt disch home day #2 cea
G8838 0010 3 Patient not discharged to home by post-operative day #2 following cea Not disch home by day #2
G8839 0010 3 Sleep apnea symptoms assessed, including presence or absence of snoring and daytime sleepiness Sleep apnea assess
G8840 0010 3 Documentation of reason(s) for not documenting an assessment of sleep symptoms (e.g., patient didn’t have initial daytime sleepiness, patient visited between initial testing and initiation of therapy) Doc reas no sleep apnea
G8841 0010 3 Sleep apnea symptoms not assessed, reason not given No sleep apnea assess
G8842 0010 3 Apnea hypopnea index (ahi) or respiratory disturbance index (rdi) measured at the time of initial diagnosis Ahi or rdi initial dx
G8843 0010 3 Documentation of reason(s) for not measuring an apnea hypopnea index (ahi) or a respiratory disturbance index (rdi) at the time of initial diagnosis (e.g., psychiatric disease, dementia, patient declined, financial, insurance coverage, test ordered but not yet completed) Doc reas no ahi or rdi
G8844 0010 3 Apnea hypopnea index (ahi) or respiratory disturbance index (rdi) not measured at the time of initial diagnosis, reason not given No ahi or rdi initial dx
G8845 0010 3 Positive airway pressure therapy prescribed Pos airway press prescribed
G8846 0010 3 Moderate or severe obstructive sleep apnea (apnea hypopnea index (ahi) or respiratory disturbance index (rdi) of 15 or greater) Mod or severe osa
G8848 0010 3 Mild obstructive sleep apnea (apnea hypopnea index (ahi) or respiratory disturbance index (rdi) of less than 15) Mild osa
G8849 0010 3 Documentation of reason(s) for not prescribing positive airway pressure therapy (e.g., patient unable to tolerate, alternative therapies use, patient declined, financial, insurance coverage) Doc reas no pos air press
G8850 0010 3 Positive airway pressure therapy not prescribed, reason not given No pap prescribed
G8851 0010 3 Objective measurement of adherence to positive airway pressure therapy, documented Adhere pos air press therapy
G8852 0010 3 Positive airway pressure therapy prescribed Pos air press prescribe
G8853 0010 3 Positive airway pressure therapy not prescribed Pos air press not prescribe
G8854 0010 3 Documentation of reason(s) for not objectively measuring adherence to positive airway pressure therapy (e.g., patient didn’t bring data from continous positive airway pressure [cpap], therapy not yet initiated, not available on machine) Reas no adhere pos air pres
G8855 0010 3 Objective measurement of adherence to positive airway pressure therapy not performed, reason not given Pos air press adhere no perf
G8856 0010 3 Referral to a physician for an otologic evaluation performed Ref for oto eval
G8857 0010 3 Patient is not eligible for the referral for otologic evaluation measure (e.g., patients who are already under the care of a physician for acute or chronic dizziness) No elig ref for oto eval
G8858 0010 3 Referral to a physician for an otologic evaluation not performed, reason not given Not ref for oto eval
G8859 0010 3 Patient receiving corticosteroids greater than or equal to 10mg/day for 60 or greater consecutive days Corticosteroids 10mg 60 days
G8860 0010 3 Patients who have received dose of corticosteroids greater than or equal to 10mg/day for 60 or greater consecutive days Corticosteroid 10 mg 60 days
G8861 0010 3 Within the past 2 years, central dual-energy x-ray absorptiometry (dxa) ordered and documented, review of systems and medication history or pharmacologic therapy (other than minerals/vitamins) for osteoporosis prescribed Dxa ordered for osteo
G8862 0010 3 Patients not receiving corticosteroids greater than or equal to 10mg/day for 60 or greater consecutive days No corticostrd 10mg 60 days
G8863 0010 3 Patients not assessed for risk of bone loss, reason not given No assess bone loss
G8864 0010 3 Pneumococcal vaccine administered or previously received Pneumococcal vaccine admin
G8865 0010 3 Documentation of medical reason(s) for not administering or previously receiving pneumococcal vaccine (e.g., patient allergic reaction, potential adverse drug reaction) Doc med reas no pneumococcal
G8866 0010 3 Documentation of patient reason(s) for not administering or previously receiving pneumococcal vaccine (e.g., patient refusal) Doc pt reas no pneumococcal
G8867 0010 3 Pneumococcal vaccine not administered or previously received, reason not given No pneumococcal admin
G8868 0010 3 Patients receiving a first course of anti-tnf therapy 1st course antitnf
G8869 0010 3 Patient has documented immunity to hepatitis b and initiating anti-tnf therapy Doc immune hep b antitnf
G8870 0010 3 Hepatitis b vaccine injection administered or previously received and is receiving a first course of anti-tnf therapy Hepb admin 1st antitnf
G8871 0010 3 Patient not receiving a first course of anti-tnf therapy No 1st antitnf
G8872 0010 3 Excised tissue evaluated by imaging intraoperatively to confirm successful inclusion of targeted lesion Intraop image confirm excise
G8873 0010 3 Patients with needle localization specimens which are not amenable to intraoperative imaging such as mri needle wire localization, or targets which are tentatively identified on mammogram or ultrasound which do not contain a biopsy marker but which can be verified on intraoperative inspection or pathology (e.g., needle biopsy site where the biopsy marker is remote from the actual biopsy site) Specimen not intraop image
G8874 0010 3 Excised tissue not evaluated by imaging intraoperatively to confirm successful inclusion of targeted lesion Tissue not image intraop
G8875 0010 3 Clinician diagnosed breast cancer preoperatively by a minimally invasive biopsy method Breast cancer dx min invsive
G8876 0010 3 Documentation of reason(s) for not performing minimally invasive biopsy to diagnose breast cancer preoperatively (e.g., lesion too close to skin, implant, chest wall, etc., lesion could not be adequately visualized for needle biopsy, patient condition prevents needle biopsy [weight, breast thickness, etc.], duct excision without imaging abnormality, prophylactic mastectomy, reduction mammoplasty, excisional biopsy performed by another physician) Doc reas no min inv dx
G8877 0010 3 Clinician did not attempt to achieve the diagnosis of breast cancer preoperatively by a minimally invasive biopsy method, reason not given No brst cncr dx min invasive
G8878 0010 3 Sentinel lymph node biopsy procedure performed Sent lymph node biopsy
G8879 0010 3 Clinically node negative (t1n0m0 or t2n0m0) invasive breast cancer Node neg inv brst cncr
G8880 0010 3 Documentation of reason(s) sentinel lymph node biopsy not performed (e.g., reasons could include but not limited to; non-invasive cancer, incidental discovery of breast cancer on prophylactic mastectomy, incidental discovery of breast cancer on reduction mammoplasty, pre-operative biopsy proven lymph node (ln) metastases, inflammatory carcinoma, stage 3 locally advanced cancer, recurrent invasive breast cancer, clinically node positive after neoadjuvant systemic therapy, patient refusal after informed consent, patient with significant age, comorbidities, or limited life expectancy and favorable tumor; adjuvant systemic therapy unlikely to change) Sen lym p node biop not perf
G8881 0010 3 Stage of breast cancer is greater than t1n0m0 or t2n0m0 Brst cncr stage > t1n0m0
G8882 0010 3 Sentinel lymph node biopsy procedure not performed, reason not given No sent lymph node biopsy
G8883 0010 3 Biopsy results reviewed, communicated, tracked and documented Rev, comm, track, doc biopsy
G8884 0010 3 Clinician documented reason that patient’s biopsy results were not reviewed Doc reas biopsy not review
G8885 0010 3 Biopsy results not reviewed, communicated, tracked or documented No rev, comm, track biopsy
G8886 0010 3 Most recent blood pressure under control Bp under control
G8887 0010 3 Documentation of medical reason(s) for most recent blood pressure not being under control (e.g., patients with palliative goals or for whom treatment of hypertension with standard treatment goals is not clinically appropriate) Doc med reas bp not control
G8888 0010 3 Most recent blood pressure not under control, results documented and reviewed Bp not under control
G8889 0010 3 No documentation of blood pressure measurement, reason not given No doc bp
G8890 0010 3 Most recent ldl-c under control, results documented and reviewed Ldl-c under control
G8891 0010 3 Documentation of medical reason(s) for most recent ldl-c not under control (e.g., patients with palliative goals for whom treatment of hypertension with standard treatment goals is not clinically appropriate) Doc med reas no ldl-c contrl
G8892 0010 3 Documentation of medical reason(s) for not performing ldl-c test (e.g. patients with palliative goals or for whom treatment of hypertension with standard treatment goals is not clinically appropriate) Doc med reas no ldl-c test
G8893 0010 3 Most recent ldl-c not under control, results documented and reviewed Ldl-c not under control
G8894 0010 3 Ldl-c not performed, reason not given Ldl-c not performed
G8895 0010 3 Oral aspirin or other antithrombotic therapy prescribed Antrom prescribe
G8896 0010 3 Documentation of medical reason(s) for not prescribing oral aspirin or other antithrombotic therapy (e.g., patient documented to be low risk or patient with terminal illness or treatment of hypertension with standard treatment goals is not clinically appropriate, or for whom risk of aspirin or other antithrombotic therapy exceeds potential benefits such as for individuals whose blood pressure is poorly controlled) Doc med reas no antihtrom
G8897 0010 3 Oral aspirin or other antithrombotic therapy was not prescribed, reason not given Antithrom not prescribe
G8898 0010 3 I intend to report the chronic obstructive pulmonary disease (copd) measures group Copd measures group
G8899 0010 3 I intend to report the inflammatory bowel disease (ibd) measures group Inflammatory bowel dis mg
G8900 0010 3 I intend to report the sleep apnea measures group Obstructive sleep apnea mg
G8902 0010 3 I intend to report the dementia measures group Dementia measures group
G8903 0010 3 I intend to report the parkinson’s disease measures group Parkinson’s disease mg
G8904 0010 3 I intend to report the hypertension (htn) measures group Hypertension mg
G8905 0010 3 I intend to report the cardiovascular prevention measures group Cardiovascular prevention mg
G8906 0010 3 I intend to report the cataract measures group Cataract measures group
G8907 0010 3 Patient documented not to have experienced any of the following events: a burn prior to discharge; a fall within the facility; wrong site/side/patient/procedure/implant event; or a hospital transfer or hospital admission upon discharge from the facility Pt doc no events on discharg
G8908 0010 3 Patient documented to have received a burn prior to discharge Pt doc w burn prior to d/c
G8909 0010 3 Patient documented not to have received a burn prior to discharge Pt doc no burn prior to d/c
G8910 0010 3 Patient documented to have experienced a fall within asc Pt doc to have fall in asc
G8911 0010 3 Patient documented not to have experienced a fall within ambulatory surgical center Pt doc no fall in asc
G8912 0010 3 Patient documented to have experienced a wrong site, wrong side, wrong patient, wrong procedure or wrong implant event Pt doc with wrong event
G8913 0010 3 Patient documented not to have experienced a wrong site, wrong side, wrong patient, wrong procedure or wrong implant event Pt doc no wrong event
G8914 0010 3 Patient documented to have experienced a hospital transfer or hospital admission upon discharge from asc Pt trans to hosp post d/c
G8915 0010 3 Patient documented not to have experienced a hospital transfer or hospital admission upon discharge from asc Pt not trans to hosp at d/c
G8916 0010 3 Patient with preoperative order for iv antibiotic surgical site infection (ssi) prophylaxis, antibiotic initiated on time Pt w iv ab given on time
G8917 0010 3 Patient with preoperative order for iv antibiotic surgical site infection (ssi) prophylaxis, antibiotic not initiated on time Pt w iv ab not given on time
G8918 0010 3 Patient without preoperative order for iv antibiotic surgical site infection (ssi) prophylaxis Pt w/o preop order iv ab pro
G8923 0010 3 Left ventricular ejection fraction (lvef) < 40% or documentation of moderately or severely depressed left ventricular systolic function Lvef < 40% or lvsd
G8924 0010 3 Spirometry test results demonstrate fev1/fvc < 70%, fev < 60% predicted and patient has copd symptoms (e.g., dyspnea, cough/sputum, wheezing) Spir fev1/fvc<70%,fev<60%
G8925 0010 3 Spirometry test results demonstrate fev1 >= 60% fev1/fvc >= 70%, predicted or patient does not have copd symptoms Spir fev1/fvc>=60% & no copd
G8926 0010 3 Spirometry test not performed or documented, reason not given Spiro no perf or doc
G8927 0010 3 Adjuvant chemotherapy referred, prescribed or previously received for ajcc stage iii, colon cancer Adj chem pres ajcc iii
G8928 0010 3 Adjuvant chemotherapy not prescribed or previously received, for documented reasons (e.g., medical co-morbidities, diagnosis date more than 5 years prior to the current visit date, patient’s diagnosis date is within 120 days of the end of the 12 month reporting period, patient’s cancer has metastasized, medical contraindication/allergy, poor performance status, other medical reasons, patient refusal, other patient reasons, patient is currently enrolled in a clinical trial that precludes prescription of chemotherapy, other system reasons) Adj chem not pres rsn spec
G8929 0010 3 Adjuvant chemotherapy not prescribed or previously received, reason not given Adj cmo not pres rsn not gvn
G8930 0010 3 Assessment of depression severity at the initial evaluation Assess of dep @ initial eval
G8931 0010 3 Assessment of depression severity not documented, reason not given Asses of dep not documented
G8932 0010 3 Suicide risk assessed at the initial evaluation Suicd rsk assessed init eval
G8933 0010 3 Suicide risk not assessed at the initial evaluation, reason not given Suicide risk not assessed
G8934 0010 3 Left ventricular ejection fraction (lvef) <40% or documentation of moderately or severely depressed left ventricular systolic function Lvef <40% or dep lv sys fcn
G8935 0010 3 Clinician prescribed angiotensin converting enzyme (ace) inhibitor or angiotensin receptor blocker (arb) therapy Rx ace or arb therapy
G8936 0010 3 Clinician documented that patient was not an eligible candidate for angiotensin converting enzyme (ace) inhibitor or angiotensin receptor blocker (arb) therapy (eg, allergy, intolerance, pregnancy, renal failure due to ace inhibitor, diseases of the aortic or mitral valve, other medical reasons) or (eg, patient declined, other patient reasons) or (eg, lack of drug availability, other reasons attributable to the health care system) Pt not eligible ace/arb
G8937 0010 3 Clinician did not prescribe angiotensin converting enzyme (ace) inhibitor or angiotensin receptor blocker (arb) therapy, reason not given No rx ace/arb therapy
G8938 0010 3 Bmi is documented as being outside of normal limits, follow-up plan is not documented, documentation the patient is not eligible Bmi doc onl fup nt doc
G8939 0010 3 Pain assessment documented as positive, follow-up plan not documented, documentation the patient is not eligible at the time of the encounter Pain as doc positive, no f/u
G8940 0010 3 Screening for depression documented as positive, a follow-up plan not completed, documented reason Scr dep pos, no plan done
G8941 0010 3 Elder maltreatment screen documented as positive, follow-up plan not documented, documentation the patient is not eligible for follow-up plan at the time of the encounter Eld maltreatment doc as pos
G8942 0010 3 Functional outcomes assessment using a standardized tool is documented within the previous 30 days and care plan, based on identified deficiencies on the date of the functional outcome assessment, is documented Doc fcn/care plan w/30 days
G8943 0010 3 Ldl-c result not present or not within 12 months prior Ldlc not pres w/i 12 mo prir
G8944 0010 3 Ajcc melanoma cancer stage 0 through iic melanoma Ajcc mel cnr stg 0 - iic
G8946 0010 3 Minimally invasive biopsy method attempted but not diagnostic of breast cancer (e.g., high risk lesion of breast such as atypical ductal hyperplasia, lobular neoplasia, atypical lobular hyperplasia, lobular carcinoma in situ, atypical columnar hyperplasia, flat epithelial atypia, radial scar, complex sclerosing lesion, papillary lesion, or any lesion with spindle cells) Mibm but no dx of breast ca
G8947 0010 3 One or more neuropsychiatric symptoms 1 or more neuropsych
G8948 0010 3 No neuropsychiatric symptoms No neuropsych symptoms
G8949 0010 3 Documentation of patient reason(s) for patient not receiving counseling for diet and physical activity (e.g., patient is not willing to discuss diet or exercise interventions to help control blood pressure, or the patient said he/she refused to make these changes) Doc pt reas on counsel diet
G8950 0010 3 Pre-hypertensive or hypertensive blood pressure reading documented, and the indicated follow-up is documented Pre-htn or htn doc, f/u indc
G8951 0010 3 Pre-hypertensive or hypertensive blood pressure reading documented, indicated follow-up not documented, documentation the patient is not eligible Pre-htn/htn doc, no pt f/u
G8952 0010 3 Pre-hypertensive or hypertensive blood pressure reading documented, indicated follow-up not documented, reason not given Pre-htn/htn, no f/u, not gvn
G8953 0010 3 All quality actions for the applicable measures in the oncology measures group have been performed for this patient Oncology mg qual act perform
G8955 0010 3 Most recent assessment of adequacy of volume management documented Most recent assess vol mgmt
G8956 0010 3 Patient receiving maintenance hemodialysis in an outpatient dialysis facility Pt rcv hedia outpt dyls fac
G8957 0010 3 Patient not receiving maintenance hemodialysis in an outpatient dialysis facility Pt no hedia in outpt fac
G8958 0010 3 Assessment of adequacy of volume management not documented, reason not given Assess vol mgmt not doc
G8959 0010 3 Clinician treating major depressive disorder communicates to clinician treating comorbid condition Clin tx mdd comm to tx clin
G8960 0010 3 Clinician treating major depressive disorder did not communicate to clinician treating comorbid condition, reason not given Clin tx mdd not comm
G8961 0010 3 Cardiac stress imaging test primarily performed on low-risk surgery patient for preoperative evaluation within 30 days preceding this surgery Csit lowrisk surg pts preop
G8962 0010 3 Cardiac stress imaging test performed on patient for any reason including those who did not have low risk surgery or test that was performed more than 30 days preceding low risk surgery Csit on pt any reas 30 days
G8963 0010 3 Cardiac stress imaging performed primarily for monitoring of asymptomatic patient who had pci within 2 years Csi per asx pt w/pci 2 yrs
G8964 0010 3 Cardiac stress imaging test performed primarily for any other reason than monitoring of asymptomatic patient who had pci within 2 years (e.g., symptomatic patient, patient greater than 2 years since pci, initial evaluation, etc) Csi any other than pci 2 yr
G8965 0010 3 Cardiac stress imaging test primarily performed on low chd risk patient for initial detection and risk assessment Csit perf on low chd rsk
G8966 0010 3 Cardiac stress imaging test performed on symptomatic or higher than low chd risk patient or for any reason other than initial detection and risk assessment Csit perf sx or high chd rsk
G8967 0010 3 Warfarin or another fda approved oral anticoagulant is prescribed Warf or other fda drug presc
G8968 0010 3 Documentation of medical reason(s) for not prescribing warfarin or another fda-approved anticoagulant (e.g., atrial appendage device in place) Doc med not presb
G8969 0010 3 Documentation of patient reason(s) for not prescribing warfarin or another fda-approved oral anticoagulant that is fda approved for the prevention of thromboembolism (e.g., patient choice of having atrial appendage device placed) Doc pt rsn no presc warf/fda
G8970 0010 3 No risk factors or one moderate risk factor for thromboembolism No rsk fac or 1 mod risk te
G8971 0010 3 Warfarin or another oral anticoagulant that is fda approved not prescribed, reason not given Warfrn or othr antcog no rx
G8972 0010 3 One or more high risk factors for thromboembolism or more than one moderate risk factor for thromboembolism 1>=risk or>= mod risk for te
G8973 0010 3 Most recent hemoglobin (hgb) level < 10 g/dl Mst rcnt hbb < 10g/dl
G8974 0010 3 Hemoglobin level measurement not documented, reason not given Hgb not doc rns not gvn
G8975 0010 3 Documentation of medical reason(s) for patient having a hemoglobin level < 10 g/dl (e.g., patients who have non-renal etiologies of anemia [e.g., sickle cell anemia or other hemoglobinopathies, hypersplenism, primary bone marrow disease, anemia related to chemotherapy for diagnosis of malignancy, postoperative bleeding, active bloodstream or peritoneal infection], other medical reasons) Hgb <10g/dl, med rsn
G8976 0010 3 Most recent hemoglobin (hgb) level >= 10 g/dl Hgb >= 10 g/dl
G8977 0010 3 I intend to report the oncology measures group Oncology measures grp
G8978 0010 3 Mobility: walking & moving around functional limitation, current status, at therapy episode outset and at reporting intervals Mobility current status
G8979 0010 3 Mobility: walking & moving around functional limitation, projected goal status, at therapy episode outset, at reporting intervals, and at discharge or to end reporting Mobility goal status
G8980 0010 3 Mobility: walking & moving around functional limitation, discharge status, at discharge from therapy or to end reporting Mobility d/c status
G8981 0010 3 Changing & maintaining body position functional limitation, current status, at therapy episode outset and at reporting intervals Body pos current status
G8982 0010 3 Changing & maintaining body position functional limitation, projected goal status, at therapy episode outset, at reporting intervals, and at discharge or to end reporting Body pos goal status
G8983 0010 3 Changing & maintaining body position functional limitation, discharge status, at discharge from therapy or to end reporting Body pos d/c status
G8984 0010 3 Carrying, moving & handling objects functional limitation, current status, at therapy episode outset and at reporting intervals Carry current status
G8985 0010 3 Carrying, moving and handling objects, projected goal status, at therapy episode outset, at reporting intervals, and at discharge or to end reporting Carry goal status
G8986 0010 3 Carrying, moving & handling objects functional limitation, discharge status, at discharge from therapy or to end reporting Carry d/c status
G8987 0010 3 Self care functional limitation, current status, at therapy episode outset and at reporting intervals Self care current status
G8988 0010 3 Self care functional limitation, projected goal status, at therapy episode outset, at reporting intervals, and at discharge or to end reporting Self care goal status
G8989 0010 3 Self care functional limitation, discharge status, at discharge from therapy or to end reporting Self care d/c status
G8990 0010 3 Other physical or occupational therapy primary functional limitation, current status, at therapy episode outset and at reporting intervals Other pt/ot current status
G8991 0010 3 Other physical or occupational therapy primary functional limitation, projected goal status, at therapy episode outset, at reporting intervals, and at discharge or to end reporting Other pt/ot goal status
G8992 0010 3 Other physical or occupational therapy primary functional limitation, discharge status, at discharge from therapy or to end reporting Other pt/ot d/c status
G8993 0010 3 Other physical or occupational therapy subsequent functional limitation, current status, at therapy episode outset and at reporting intervals Sub pt/ot current status
G8994 0010 3 Other physical or occupational therapy subsequent functional limitation, projected goal status, at therapy episode outset, at reporting intervals, and at discharge or to end reporting Sub pt/ot goal status
G8995 0010 3 Other physical or occupational therapy subsequent functional limitation, discharge status, at discharge from therapy or to end reporting Sub pt/ot d/c status
G8996 0010 3 Swallowing functional limitation, current status at therapy episode outset and at reporting intervals Swallow current status
G8997 0010 3 Swallowing functional limitation, projected goal status, at therapy episode outset, at reporting intervals, and at discharge or to end reporting Swallow goal status
G8998 0010 3 Swallowing functional limitation, discharge status, at discharge from therapy or to end reporting Swallow d/c status
G8999 0010 3 Motor speech functional limitation, current status at therapy episode outset and at reporting intervals Motor speech current status
G9001 0010 3 Coordinated care fee, initial rate Mccd, initial rate
G9002 0010 3 Coordinated care fee, maintenance rate Mccd,maintenance rate
G9003 0010 3 Coordinated care fee, risk adjusted high, initial Mccd, risk adj hi, initial
G9004 0010 3 Coordinated care fee, risk adjusted low, initial Mccd, risk adj lo, initial
G9005 0010 3 Coordinated care fee, risk adjusted maintenance Mccd, risk adj, maintenance
G9006 0010 3 Coordinated care fee, home monitoring Mccd, home monitoring
G9007 0010 3 Coordinated care fee, scheduled team conference Mccd, sch team conf
G9008 0010 3 Coordinated care fee, physician coordinated care oversight services Mccd,phys coor-care ovrsght
G9009 0010 3 Coordinated care fee, risk adjusted maintenance, level 3 Mccd, risk adj, level 3
G9010 0010 3 Coordinated care fee, risk adjusted maintenance, level 4 Mccd, risk adj, level 4
G9011 0010 3 Coordinated care fee, risk adjusted maintenance, level 5 Mccd, risk adj, level 5
G9012 0010 3 Other specified case management service not elsewhere classified Other specified case mgmt
G9013 0010 3 Esrd demo basic bundle level i Esrd demo bundle level i
G9014 0010 3 Esrd demo expanded bundle including venous access and related services Esrd demo bundle-level ii
G9016 0010 3 Smoking cessation counseling, individual, in the absence of or in addition to any other evaluation and management service, per session (6-10 minutes) [demo project code only] Demo-smoking cessation coun
G9017 0010 3 Amantadine hydrochloride, oral, per 100 mg (for use in a medicare-approved demonstration project) Amantadine hcl 100mg oral
G9018 0010 3 Zanamivir, inhalation powder, administered through inhaler, per 10 mg (for use in a medicare-approved demonstration project) Zanamivir,inhalation pwd 10m
G9019 0010 3 Oseltamivir phosphate, oral, per 75 mg (for use in a medicare-approved demonstration project) Oseltamivir phosphate 75mg
G9020 0010 3 Rimantadine hydrochloride, oral, per 100 mg (for use in a medicare-approved demonstration project) Rimantadine hcl 100mg oral
G9033 0010 3 Amantadine hydrochloride, oral brand, per 100 mg (for use in a medicare-approved demonstration project) Amantadine hcl oral brand
G9034 0010 3 Zanamivir, inhalation powder, administered through inhaler, brand, per 10 mg (for use in a medicare-approved demonstration project) Zanamivir, inh pwdr, brand
G9035 0010 3 Oseltamivir phosphate, oral, brand, per 75 mg (for use in a medicare-approved demonstration project) Oseltamivir phosp, brand
G9036 0010 3 Rimantadine hydrochloride, oral, brand, per 100 mg (for use in a medicare-approved demonstration project) Rimantadine hcl, brand
G9050 0010 3 Oncology; primary focus of visit; work-up, evaluation, or staging at the time of cancer diagnosis or recurrence (for use in a medicare-approved demonstration project) Oncology work-up evaluation
G9051 0010 3 Oncology; primary focus of visit; treatment decision-making after disease is staged or restaged, discussion of treatment options, supervising/coordinating active cancer directed therapy or managing consequences of cancer directed therapy (for use in a medicare-approved demonstration project) Oncology tx decision-mgmt
G9052 0010 3 Oncology; primary focus of visit; surveillance for disease recurrence for patient who has completed definitive cancer-directed therapy and currently lacks evidence of recurrent disease; cancer directed therapy might be considered in the future (for use in a medicare-approved demonstration project) Onc surveillance for disease
G9053 0010 3 Oncology; primary focus of visit; expectant management of patient with evidence of cancer for whom no cancer directed therapy is being administered or arranged at present; cancer directed therapy might be considered in the future (for use in a medicare-approved demonstration project) Onc expectant management pt
G9054 0010 3 Oncology; primary focus of visit; supervising, coordinating or managing care of patient with terminal cancer or for whom other medical illness prevents further cancer treatment; includes symptom management, end-of-life care planning, management of palliative therapies (for use in a medicare-approved demonstration project) Onc supervision palliative
G9055 0010 3 Oncology; primary focus of visit; other, unspecified service not otherwise listed (for use in a medicare-approved demonstration project) Onc visit unspecified nos
G9056 0010 3 Oncology; practice guidelines; management adheres to guidelines (for use in a medicare-approved demonstration project) Onc prac mgmt adheres guide
G9057 0010 3 Oncology; practice guidelines; management differs from guidelines as a result of patient enrollment in an institutional review board approved clinical trial (for use in a medicare-approved demonstration project) Onc pract mgmt differs trial
G9058 0010 3 Oncology; practice guidelines; management differs from guidelines because the treating physician disagrees with guideline recommendations (for use in a medicare-approved demonstration project) Onc prac mgmt disagree w/gui
G9059 0010 3 Oncology; practice guidelines; management differs from guidelines because the patient, after being offered treatment consistent with guidelines, has opted for alternative treatment or management, including no treatment (for use in a medicare-approved demonstration project) Onc prac mgmt pt opt alterna
G9060 0010 3 Oncology; practice guidelines; management differs from guidelines for reason(s) associated with patient comorbid illness or performance status not factored into guidelines (for use in a medicare-approved demonstration project) Onc prac mgmt dif pt comorb
G9061 0010 3 Oncology; practice guidelines; patient’s condition not addressed by available guidelines (for use in a medicare-approved demonstration project) Onc prac cond noadd by guide
G9062 0010 3 Oncology; practice guidelines; management differs from guidelines for other reason(s) not listed (for use in a medicare-approved demonstration project) Onc prac guide differs nos
G9063 0010 3 Oncology; disease status; limited to non-small cell lung cancer; extent of disease initially established as stage i (prior to neo-adjuvant therapy, if any) with no evidence of disease progression, recurrence, or metastases (for use in a medicare-approved demonstration project) Onc dx nsclc stgi no progres
G9064 0010 3 Oncology; disease status; limited to non-small cell lung cancer; extent of disease initially established as stage ii (prior to neo-adjuvant therapy, if any) with no evidence of disease progression, recurrence, or metastases (for use in a medicare-approved demonstration project) Onc dx nsclc stg2 no progres
G9065 0010 3 Oncology; disease status; limited to non-small cell lung cancer; extent of disease initially established as stage iii a (prior to neo-adjuvant therapy, if any) with no evidence of disease progression, recurrence, or metastases (for use in a medicare-approved demonstration project) Onc dx nsclc stg3a no progre
G9066 0010 3 Oncology; disease status; limited to non-small cell lung cancer; stage iii b- iv at diagnosis, metastatic, locally recurrent, or progressive (for use in a medicare-approved demonstration project) Onc dx nsclc stg3b-4 metasta
G9067 0010 3 Oncology; disease status; limited to non-small cell lung cancer; extent of disease unknown, staging in progress, or not listed (for use in a medicare-approved demonstration project) Onc dx nsclc dx unknown nos
G9068 0010 3 Oncology; disease status; limited to small cell and combined small cell/non-small cell; extent of disease initially established as limited with no evidence of disease progression, recurrence, or metastases (for use in a medicare-approved demonstration project) Onc dx sclc/nsclc limited
G9069 0010 3 Oncology; disease status; small cell lung cancer, limited to small cell and combined small cell/non-small cell; extensive stage at diagnosis, metastatic, locally recurrent, or progressive (for use in a medicare-approved demonstration project) Onc dx sclc/nsclc ext at dx
G9070 0010 3 Oncology; disease status; small cell lung cancer, limited to small cell and combined small cell/non-small; extent of disease unknown, staging in progress, or not listed (for use in a medicare-approved demonstration project) Onc dx sclc/nsclc ext unknwn
G9071 0010 3 Oncology; disease status; invasive female breast cancer (does not include ductal carcinoma in situ); adenocarcinoma as predominant cell type; stage i or stage iia-iib; or t3, n1, m0; and er and/or pr positive; with no evidence of disease progression, recurrence, or metastases (for use in a medicare-approved demonstration project) Onc dx brst stg1-2b hr,nopro
G9072 0010 3 Oncology; disease status; invasive female breast cancer (does not include ductal carcinoma in situ); adenocarcinoma as predominant cell type; stage i, or stage iia-iib; or t3, n1, m0; and er and pr negative; with no evidence of disease progression, recurrence, or metastases (for use in a medicare-approved demonstration project) Onc dx brst stg1-2 noprogres
G9073 0010 3 Oncology; disease status; invasive female breast cancer (does not include ductal carcinoma in situ); adenocarcinoma as predominant cell type; stage iiia-iiib; and not t3, n1, m0; and er and/or pr positive; with no evidence of disease progression, recurrence, or metastases (for use in a medicare-approved demonstration project) Onc dx brst stg3-hr, no pro
G9074 0010 3 Oncology; disease status; invasive female breast cancer (does not include ductal carcinoma in situ); adenocarcinoma as predominant cell type; stage iiia-iiib; and not t3, n1, m0; and er and pr negative; with no evidence of disease progression, recurrence, or metastases (for use in a medicare-approved demonstration project) Onc dx brst stg3-noprogress
G9075 0010 3 Oncology; disease status; invasive female breast cancer (does not include ductal carcinoma in situ); adenocarcinoma as predominant cell type; m1 at diagnosis, metastatic, locally recurrent, or progressive (for use in a medicare-approved demonstration project) Onc dx brst metastic/ recur
G9077 0010 3 Oncology; disease status; prostate cancer, limited to adenocarcinoma as predominant cell type; t1-t2c and gleason 2-7 and psa < or equal to 20 at diagnosis with no evidence of disease progression, recurrence, or metastases (for use in a medicare-approved demonstration project) Onc dx prostate t1no progres
G9078 0010 3 Oncology; disease status; prostate cancer, limited to adenocarcinoma as predominant cell type; t2 or t3a gleason 8-10 or psa > 20 at diagnosis with no evidence of disease progression, recurrence, or metastases (for use in a medicare-approved demonstration project) Onc dx prostate t2no progres
G9079 0010 3 Oncology; disease status; prostate cancer, limited to adenocarcinoma as predominant cell type; t3b-t4, any n; any t, n1 at diagnosis with no evidence of disease progression, recurrence, or metastases (for use in a medicare-approved demonstration project) Onc dx prostate t3b-t4noprog
G9080 0010 3 Oncology; disease status; prostate cancer, limited to adenocarcinoma; after initial treatment with rising psa or failure of psa decline (for use in a medicare-approved demonstration project) Onc dx prostate w/rise psa
G9083 0010 3 Oncology; disease status; prostate cancer, limited to adenocarcinoma; extent of disease unknown, staging in progress, or not listed (for use in a medicare-approved demonstration project) Onc dx prostate unknwn nos
G9084 0010 3 Oncology; disease status; colon cancer, limited to invasive cancer, adenocarcinoma as predominant cell type; extent of disease initially established as t1-3, n0, m0 with no evidence of disease progression, recurrence, or metastases (for use in a medicare-approved demonstration project) Onc dx colon t1-3,n1-2,no pr
G9085 0010 3 Oncology; disease status; colon cancer, limited to invasive cancer, adenocarcinoma as predominant cell type; extent of disease initially established as t4, n0, m0 with no evidence of disease progression, recurrence, or metastases (for use in a medicare-approved demonstration project) Onc dx colon t4, n0 w/o prog
G9086 0010 3 Oncology; disease status; colon cancer, limited to invasive cancer, adenocarcinoma as predominant cell type; extent of disease initially established as t1-4, n1-2, m0 with no evidence of disease progression, recurrence, or metastases (for use in a medicare-approved demonstration project) Onc dx colon t1-4 no dx prog
G9087 0010 3 Oncology; disease status; colon cancer, limited to invasive cancer, adenocarcinoma as predominant cell type; m1 at diagnosis, metastatic, locally recurrent, or progressive with current clinical, radiologic, or biochemical evidence of disease (for use in a medicare-approved demonstration project) Onc dx colon metas evid dx
G9088 0010 3 Oncology; disease status; colon cancer, limited to invasive cancer, adenocarcinoma as predominant cell type; m1 at diagnosis, metastatic, locally recurrent, or progressive without current clinical, radiologic, or biochemical evidence of disease (for use in a medicare-approved demonstration project) Onc dx colon metas noevid dx
G9089 0010 3 Oncology; disease status; colon cancer, limited to invasive cancer, adenocarcinoma as predominant cell type; extent of disease unknown, staging in progress, or not listed (for use in a medicare-approved demonstration project) Onc dx colon extent unknown
G9090 0010 3 Oncology; disease status; rectal cancer, limited to invasive cancer, adenocarcinoma as predominant cell type; extent of disease initially established as t1-2, n0, m0 (prior to neo-adjuvant therapy, if any) with no evidence of disease progression, recurrence, or metastases (for use in a medicare-approved demonstration project) Onc dx rectal t1-2 no progr
G9091 0010 3 Oncology; disease status; rectal cancer, limited to invasive cancer, adenocarcinoma as predominant cell type; extent of disease initially established as t3, n0, m0 (prior to neo-adjuvant therapy, if any) with no evidence of disease progression, recurrence, or metastases (for use in a medicare-approved demonstration project) Onc dx rectal t3 n0 no prog
G9092 0010 3 Oncology; disease status; rectal cancer, limited to invasive cancer, adenocarcinoma as predominant cell type; extent of disease initially established as t1-3, n1-2, m0 (prior to neo-adjuvant therapy, if any) with no evidence of disease progression, recurrence or metastases (for use in a medicare-approved demonstration project) Onc dx rectal t1-3,n1-2noprg
G9093 0010 3 Oncology; disease status; rectal cancer, limited to invasive cancer, adenocarcinoma as predominant cell type; extent of disease initially established as t4, any n, m0 (prior to neo-adjuvant therapy, if any) with no evidence of disease progression, recurrence, or metastases (for use in a medicare-approved demonstration project) Onc dx rectal t4,n,m0 no prg
G9094 0010 3 Oncology; disease status; rectal cancer, limited to invasive cancer, adenocarcinoma as predominant cell type; m1 at diagnosis, metastatic, locally recurrent, or progressive (for use in a medicare-approved demonstration project) Onc dx rectal m1 w/mets prog
G9095 0010 3 Oncology; disease status; rectal cancer, limited to invasive cancer, adenocarcinoma as predominant cell type; extent of disease unknown, staging in progress, or not listed (for use in a medicare-approved demonstration project) Onc dx rectal extent unknwn
G9096 0010 3 Oncology; disease status; esophageal cancer, limited to adenocarcinoma or squamous cell carcinoma as predominant cell type; extent of disease initially established as t1-t3, n0-n1 or nx (prior to neo-adjuvant therapy, if any) with no evidence of disease progression, recurrence, or metastases (for use in a medicare-approved demonstration project) Onc dx esophag t1-t3 noprog
G9097 0010 3 Oncology; disease status; esophageal cancer, limited to adenocarcinoma or squamous cell carcinoma as predominant cell type; extent of disease initially established as t4, any n, m0 (prior to neo-adjuvant therapy, if any) with no evidence of disease progression, recurrence, or metastases (for use in a medicare-approved demonstration project) Onc dx esophageal t4 no prog
G9098 0010 3 Oncology; disease status; esophageal cancer, limited to adenocarcinoma or squamous cell carcinoma as predominant cell type; m1 at diagnosis, metastatic, locally recurrent, or progressive (for use in a medicare-approved demonstration project) Onc dx esophageal mets recur
G9099 0010 3 Oncology; disease status; esophageal cancer, limited to adenocarcinoma or squamous cell carcinoma as predominant cell type; extent of disease unknown, staging in progress, or not listed (for use in a medicare-approved demonstration project) Onc dx esophageal unknown
G9100 0010 3 Oncology; disease status; gastric cancer, limited to adenocarcinoma as predominant cell type; post r0 resection (with or without neoadjuvant therapy) with no evidence of disease recurrence, progression, or metastases (for use in a medicare-approved demonstration project) Onc dx gastric no recurrence
G9101 0010 3 Oncology; disease status; gastric cancer, limited to adenocarcinoma as predominant cell type; post r1 or r2 resection (with or without neoadjuvant therapy) with no evidence of disease progression, or metastases (for use in a medicare-approved demonstration project) Onc dx gastric p r1-r2noprog
G9102 0010 3 Oncology; disease status; gastric cancer, limited to adenocarcinoma as predominant cell type; clinical or pathologic m0, unresectable with no evidence of disease progression, or metastases (for use in a medicare-approved demonstration project) Onc dx gastric unresectable
G9103 0010 3 Oncology; disease status; gastric cancer, limited to adenocarcinoma as predominant cell type; clinical or pathologic m1 at diagnosis, metastatic, locally recurrent, or progressive (for use in a medicare-approved demonstration project) Onc dx gastric recurrent
G9104 0010 3 Oncology; disease status; gastric cancer, limited to adenocarcinoma as predominant cell type; extent of disease unknown, staging in progress, or not listed (for use in a medicare-approved demonstration project) Onc dx gastric unknown nos
G9105 0010 3 Oncology; disease status; pancreatic cancer, limited to adenocarcinoma as predominant cell type; post r0 resection without evidence of disease progression, recurrence, or metastases (for use in a medicare-approved demonstration project) Onc dx pancreatc p r0 res no
G9106 0010 3 Oncology; disease status; pancreatic cancer, limited to adenocarcinoma; post r1 or r2 resection with no evidence of disease progression, or metastases (for use in a medicare-approved demonstration project) Onc dx pancreatc p r1/r2 no
G9107 0010 3 Oncology; disease status; pancreatic cancer, limited to adenocarcinoma; unresectable at diagnosis, m1 at diagnosis, metastatic, locally recurrent, or progressive (for use in a medicare-approved demonstration project) Onc dx pancreatic unresectab
G9108 0010 3 Oncology; disease status; pancreatic cancer, limited to adenocarcinoma; extent of disease unknown, staging in progress, or not listed (for use in a medicare-approved demonstration project) Onc dx pancreatic unknwn nos
G9109 0010 3 Oncology; disease status; head and neck cancer, limited to cancers of oral cavity, pharynx and larynx with squamous cell as predominant cell type; extent of disease initially established as t1-t2 and n0, m0 (prior to neo-adjuvant therapy, if any) with no evidence of disease progression, recurrence, or metastases (for use in a medicare-approved demonstration project) Onc dx head/neck t1-t2no prg
G9110 0010 3 Oncology; disease status; head and neck cancer, limited to cancers of oral cavity, pharynx and larynx with squamous cell as predominant cell type; extent of disease initially established as t3-4 and/or n1-3, m0 (prior to neo-adjuvant therapy, if any) with no evidence of disease progression, recurrence, or metastases (for use in a medicare-approved demonstration project) Onc dx head/neck t3-4 noprog
G9111 0010 3 Oncology; disease status; head and neck cancer, limited to cancers of oral cavity, pharynx and larynx with squamous cell as predominant cell type; m1 at diagnosis, metastatic, locally recurrent, or progressive (for use in a medicare-approved demonstration project) Onc dx head/neck m1 mets rec
G9112 0010 3 Oncology; disease status; head and neck cancer, limited to cancers of oral cavity, pharynx and larynx with squamous cell as predominant cell type; extent of disease unknown, staging in progress, or not listed (for use in a medicare-approved demonstration project) Onc dx head/neck ext unknown
G9113 0010 3 Oncology; disease status; ovarian cancer, limited to epithelial cancer; pathologic stage ia-b (grade 1) without evidence of disease progression, recurrence, or metastases (for use in a medicare-approved demonstration project) Onc dx ovarian stg1a-b no pr
G9114 0010 3 Oncology; disease status; ovarian cancer, limited to epithelial cancer; pathologic stage ia-b (grade 2-3); or stage ic (all grades); or stage ii; without evidence of disease progression, recurrence, or metastases (for use in a medicare-approved demonstration project) Onc dx ovarian stg1a-b or 2
G9115 0010 3 Oncology; disease status; ovarian cancer, limited to epithelial cancer; pathologic stage iii-iv; without evidence of progression, recurrence, or metastases (for use in a medicare-approved demonstration project) Onc dx ovarian stg3/4 noprog
G9116 0010 3 Oncology; disease status; ovarian cancer, limited to epithelial cancer; evidence of disease progression, or recurrence, and/or platinum resistance (for use in a medicare-approved demonstration project) Onc dx ovarian recurrence
G9117 0010 3 Oncology; disease status; ovarian cancer, limited to epithelial cancer; extent of disease unknown, staging in progress, or not listed (for use in a medicare-approved demonstration project) Onc dx ovarian unknown nos
G9123 0010 3 Oncology; disease status; chronic myelogenous leukemia, limited to philadelphia chromosome positive and/or bcr-abl positive; chronic phase not in hematologic, cytogenetic, or molecular remission (for use in a medicare-approved demonstration project) Onc dx cml chronic phase
G9124 0010 3 Oncology; disease status; chronic myelogenous leukemia, limited to philadelphia chromosome positive and/or bcr-abl positive; accelerated phase not in hematologic cytogenetic, or molecular remission (for use in a medicare-approved demonstration project) Onc dx cml acceler phase
G9125 0010 3 Oncology; disease status; chronic myelogenous leukemia, limited to philadelphia chromosome positive and/or bcr-abl positive; blast phase not in hematologic, cytogenetic, or molecular remission (for use in a medicare-approved demonstration project) Onc dx cml blast phase
G9126 0010 3 Oncology; disease status; chronic myelogenous leukemia, limited to philadelphia chromosome positive and/or bcr-abl positive; in hematologic, cytogenetic, or molecular remission (for use in a medicare-approved demonstration project) Onc dx cml remission
G9128 0010 3 Oncology; disease status; limited to multiple myeloma, systemic disease; smoldering, stage i (for use in a medicare-approved demonstration project) Onc dx multi myeloma stage i
G9129 0010 3 Oncology; disease status; limited to multiple myeloma, systemic disease; stage ii or higher (for use in a medicare-approved demonstration project) Onc dx mult myeloma stg2 hig
G9130 0010 3 Oncology; disease status; limited to multiple myeloma, systemic disease; extent of disease unknown, staging in progress, or not listed (for use in a medicare-approved demonstration project) Onc dx multi myeloma unknown
G9131 0010 3 Oncology; disease status; invasive female breast cancer (does not include ductal carcinoma in situ); adenocarcinoma as predominant cell type; extent of disease unknown, staging in progress, or not listed (for use in a medicare-approved demonstration project) Onc dx brst unknown nos
G9132 0010 3 Oncology; disease status; prostate cancer, limited to adenocarcinoma; hormone-refractory/androgen-independent (e.g., rising psa on anti-androgen therapy or post-orchiectomy); clinical metastases (for use in a medicare-approved demonstration project) Onc dx prostate mets no cast
G9133 0010 3 Oncology; disease status; prostate cancer, limited to adenocarcinoma; hormone-responsive; clinical metastases or m1 at diagnosis (for use in a medicare-approved demonstration project) Onc dx prostate clinical met
G9134 0010 3 Oncology; disease status; non-hodgkin’s lymphoma, any cellular classification; stage i, ii at diagnosis, not relapsed, not refractory (for use in a medicare-approved demonstration project) Onc nhlstg 1-2 no relap no
G9135 0010 3 Oncology; disease status; non-hodgkin’s lymphoma, any cellular classification; stage iii, iv, not relapsed, not refractory (for use in a medicare-approved demonstration project) Onc dx nhl stg 3-4 not relap
G9136 0010 3 Oncology; disease status; non-hodgkin’s lymphoma, transformed from original cellular diagnosis to a second cellular classification (for use in a medicare-approved demonstration project) Onc dx nhl trans to lg bcell
G9137 0010 3 Oncology; disease status; non-hodgkin’s lymphoma, any cellular classification; relapsed/refractory (for use in a medicare-approved demonstration project) Onc dx nhl relapse/refractor
G9138 0010 3 Oncology; disease status; non-hodgkin’s lymphoma, any cellular classification; diagnostic evaluation, stage not determined, evaluation of possible relapse or non-response to therapy, or not listed (for use in a medicare-approved demonstration project) Onc dx nhl stg unknown
G9139 0010 3 Oncology; disease status; chronic myelogenous leukemia, limited to philadelphia chromosome positive and/or bcr-abl positive; extent of disease unknown, staging in progress, not listed (for use in a medicare-approved demonstration project) Onc dx cml dx status unknown
G9140 0010 3 Frontier extended stay clinic demonstration; for a patient stay in a clinic approved for the cms demonstration project; the following measures should be present: the stay must be equal to or greater than 4 hours; weather or other conditions must prevent transfer or the case falls into a category of monitoring and observation cases that are permitted by the rules of the demonstration; there is a maximum frontier extended stay clinic (fesc) visit of 48 hours, except in the case when weather or other conditions prevent transfer; payment is made on each period up to 4 hours, after the first 4 hours Frontier extended stay demo
G9143 0010 3 Warfarin responsiveness testing by genetic technique using any method, any number of specimen(s) Warfarin respon genetic test
G9147 0010 3 Outpatient intravenous insulin treatment (oivit) either pulsatile or continuous, by any means, guided by the results of measurements for: respiratory quotient; and/or, urine urea nitrogen (uun); and/or, arterial, venous or capillary glucose; and/or potassium concentration Outpt iv insulin tx any mea
G9148 0010 3 National committee for quality assurance - level 1 medical home Medical home level 1
G9149 0010 3 National committee for quality assurance - level 2 medical home Medical home level ii
G9150 0010 3 National committee for quality assurance - level 3 medical home Medical home level iii
G9151 0010 3 Mapcp demonstration - state provided services Mapcp demo state
G9152 0010 3 Mapcp demonstration - community health teams Mapcp demo community
G9153 0010 3 Mapcp demonstration - physician incentive pool Mapcp demo physician
G9156 0010 3 Evaluation for wheelchair requiring face to face visit with physician Evaluation for wheelchair
G9157 0010 3 Transesophageal doppler measurement of cardiac output (including probe placement, image acquisition, and interpretation per course of treatment) for monitoring purposes Transesoph doppl cardiac mon
G9158 0010 3 Motor speech functional limitation, discharge status, at discharge from therapy or to end reporting Motor speech d/c status
G9159 0010 3 Spoken language comprehension functional limitation, current status at therapy episode outset and at reporting intervals Lang comp current status
G9160 0010 3 Spoken language comprehension functional limitation, projected goal status at therapy episode outset, at reporting intervals, and at discharge or to end reporting Lang comp goal status
G9161 0010 3 Spoken language comprehension functional limitation, discharge status, at discharge from therapy or to end reporting Lang comp d/c status
G9162 0010 3 Spoken language expression functional limitation, current status at therapy episode outset and at reporting intervals Lang express current status
G9163 0010 3 Spoken language expression functional limitation, projected goal status at therapy episode outset, at reporting intervals, and at discharge or to end reporting Lang express goal status
G9164 0010 3 Spoken language expression functional limitation, discharge status at discharge from therapy or to end reporting Lang express d/c status
G9165 0010 3 Attention functional limitation, current status at therapy episode outset and at reporting intervals Atten current status
G9166 0010 3 Attention functional limitation, projected goal status at therapy episode outset, at reporting intervals, and at discharge or to end reporting Atten goal status
G9167 0010 3 Attention functional limitation, discharge status at discharge from therapy or to end reporting Atten d/c status
G9168 0010 3 Memory functional limitation, current status at therapy episode outset and at reporting intervals Memory current status
G9169 0010 3 Memory functional limitation, projected goal status at therapy episode outset, at reporting intervals, and at discharge or to end reporting Memory goal status
G9170 0010 3 Memory functional limitation, discharge status at discharge from therapy or to end reporting Memory d/c status
G9171 0010 3 Voice functional limitation, current status at therapy episode outset and at reporting intervals Voice current status
G9172 0010 3 Voice functional limitation, projected goal status at therapy episode outset, at reporting intervals, and at discharge or to end reporting Voice goal status
G9173 0010 3 Voice functional limitation, discharge status at discharge from therapy or to end reporting Voice d/c status
G9174 0010 3 Other speech language pathology functional limitation, current status at therapy episode outset and at reporting intervals Speech lang current status
G9175 0010 3 Other speech language pathology functional limitation, projected goal status at therapy episode outset, at reporting intervals, and at discharge or to end reporting Speech lang goal status
G9176 0010 3 Other speech language pathology functional limitation, discharge status at discharge from therapy or to end reporting Speech lang d/c status
G9186 0010 3 Motor speech functional limitation, projected goal status at therapy episode outset, at reporting intervals, and at discharge or to end reporting Motor speech goal status
G9187 0010 3 Bundled payments for care improvement initiative home visit for patient assessment performed by a qualified health care professional for individuals not considered homebound including, but not limited to, assessment of safety, falls, clinical status, fluid status, medication reconciliation/management, patient compliance with orders/plan of care, performance of activities of daily living, appropriateness of care setting; (for use only in the meidcare-approved bundled payments for care improvement initiative); may not be billed for a 30-day period covered by a transitional care management code Bpci home visit
G9188 0010 3 Beta-blocker therapy not prescribed, reason not given Beta not given no reason
G9189 0010 3 Beta-blocker therapy prescribed or currently being taken Beta pres or already taking
G9190 0010 3 Documentation of medical reason(s) for not prescribing beta-blocker therapy (eg, allergy, intolerance, other medical reasons) Medical reason for no beta
G9191 0010 3 Documentation of patient reason(s) for not prescribing beta-blocker therapy (eg, patient declined, other patient reasons) Pt reason for no beta
G9192 0010 3 Documentation of system reason(s) for not prescribing beta-blocker therapy (eg, other reasons attributable to the health care system) System reason for no beta
G9193 0010 3 Clinician documented that patient with a diagnosis of major depression was not an eligible candidate for antidepressant medication treatment or patient did not have a diagnosis of major depression Doc not eligible for dep med
G9194 0010 3 Patient with a diagnosis of major depression documented as being treated with antidepressant medication during the entire 180 day (6 month) continuation treatment phase Mdd pt treated for 180d
G9195 0010 3 Patient with a diagnosis of major depression not documented as being treated with antidepressant medication during the entire 180 day (6 months) continuation treatment phase Mdd pt not treated for 180d
G9196 0010 3 Documentation of medical reason(s) for not ordering a first or second generation cephalosporin for antimicrobial prophylaxis (e.g., patients enrolled in clinical trials, patients with documented infection prior to surgical procedure of interest, patients who were receiving antibiotics more than 24 hours prior to surgery [except colon surgery patients taking oral prophylactic antibiotics], patients who were receiving antibiotics within 24 hours prior to arrival [except colon surgery patients taking oral prophylactic antibiotics], other medical reason(s)) Med reason for no ceph
G9197 0010 3 Documentation of order for first or second generation cephalosporin for antimicrobial prophylaxis Order for ceph
G9198 0010 3 Order for first or second generation cephalosporin for antimicrobial prophylaxis was not documented, reason not given No order for ceph no reason
G9199 0010 3 Venous thromboembolism (vte) prophylaxis not administered the day of or the day after hospital admission for documented reasons (eg, patient is ambulatory, patient expired during inpatient stay, patient already on warfarin or another anticoagulant, other medical reason(s) or eg, patient left against medical advice, other patient reason(s)) Doc reason for no vte
G9200 0010 3 Venous thromboembolism (vte) prophylaxis was not administered the day of or the day after hospital admission, reason not given No reason for no vte
G9201 0010 3 Venous thromboembolism (vte) prophylaxis administered the day of or the day after hospital admission Vte given upon admission
G9202 0010 3 Patients with a positive hepatitis c antibody test Hep c aby pos
G9203 0010 3 Rna testing for hepatitis c documented as performed within 12 months prior to initiation of antiviral treatment for hepatitis c Hep c rna done prior to med
G9204 0010 3 Rna testing for hepatitis c was not documented as performed within 12 months prior to initiation of antiviral treatment for hepatitis c, reason not given No reason for no hep c rna
G9205 0010 3 Patient starting antiviral treatmentfor hepatitis c during the measurement period Hep c antiviral started
G9206 0010 3 Patient starting antiviral treatment for hepatitis c during the measurement period Hep c therapy started
G9207 0010 3 Hepatitis c genotype testing documented as performed within 12 months prior to initiation of antiviral treatment for hepatitis c Hep c genotype prior to med
G9208 0010 3 Hepatitis c genotype testing was not documented as performed within 12 months prior to initiation of antiviral treatment for hepatitis c, reason not given No reason for no hep c geno
G9209 0010 3 Hepatitis c quantitative rna testing documented as performed between 4-12 weeks after the initiation of antiviral treatment Hep c rna 4to12 wk after med
G9210 0010 3 Hepatitis c quantitative rna testing not performed between 4-12 weeks after the initiation of antiviral treatment for documented reason(s) (e.g., patients whose treatment was discontinued during the testing period prior to testing, other medical reasons, patient declined, other patient reasons) No hepc rna after med docrsn
G9211 0010 3 Hepatitis c quantitative rna testing was not documented as performed between 4-12 weeks after the initiation of antiviral treatment, reason not given No hepc rna after med no rsn
G9212 0010 3 Dsm-ivtm criteria for major depressive disorder documented at the initial evaluation Doc of dsm-iv init eval
G9213 0010 3 Dsm-iv-tr criteria for major depressive disorder not documented at the initial evaluation, reason not otherwise specified No doc of dsm-iv
G9214 0010 3 Cd4+ cell count or cd4+ cell percentage results documented Cd4 count documented
G9215 0010 3 Cd4+ cell count or percentage not documented as performed, reason not given No cd4 count no reason
G9216 0010 3 Pcp prophylaxis was not prescribed at time of diagnosis of hiv, reason not given No pcp proph at dx no reason
G9217 0010 3 Pcp prophylaxis was not prescribed within 3 months of low cd4+ cell count below 200 cells/mm3, reason not given No pcp proph low cd4 norsn
G9218 0010 3 Pcp prophylaxis was not prescribed within 3 months oflow cd4+ cell count below 500 cells/mm3 or a cd4 percentage below 15%, reason not given No pcp prop low at cd4 norsn
G9219 0010 3 Pneumocystis jiroveci pneumonia prophylaxis not prescribed within 3 months of low cd4+ cell count below 200 cells/mm3 for medical reason (i.e., patient’s cd4+ cell count above threshold within 3 months after cd4+ cell count below threshold, indicating that the patient’s cd4+ levels are within an acceptable range and the patient does not require pcp prophylaxis) No oder pjp for med reason
G9220 0010 3 Pneumocystis jiroveci pneumonia prophylaxis not prescribed within 3 months of low cd4+ cell count below 500 cells/mm3 or a cd4 percentage below 15% for medical reason (i.e., patient’s cd4+ cell count above threshold within 3 months after cd4+ cell count below threshold, indicating that the patient’s cd4+ levels are within an acceptable range and the patient does not require pcp prophylaxis) No order for pjp for medrsn
G9221 0010 3 Pneumocystis jiroveci pneumonia prophlaxis prescribed Pjp proph prescribed
G9222 0010 3 Pneumocystis jiroveci pneumonia prophylaxis prescribed wthin 3 months of low cd4+ cell count below 200 cells/mm3 Pjp proph ordered low cd4
G9223 0010 3 Pneumocystis jiroveci pneumonia prophylaxis prescribed within 3 months of low cd4+ cell count below 500 cells/mm3 or a cd4 percentage below 15% Pjp proph ordered cd4 low
G9224 0010 3 Documentation of medical reason for not performing foot exam (e.g., patient with bilateral foot/leg amputation) Medrsn no foot exam
G9225 0010 3 Foot exam was not performed, reason not given Norsn no foot exam
G9226 0010 3 Foot examination performed (includes examination through visual inspection, sensory exam with 10-g monofilament plus testing any one of the following: vibration using 128-hz tuning fork, pinprick sensation, ankle reflexes, or vibration perception threshold, and pulse exam; report when all of the 3 components are completed) 3 comp foot exam completed
G9227 0010 3 Functional outcome assessment documented, care plan not documented, documentation the patient is not eligible for a care plan at the time of the encounter Foa doc, care plan not doc
G9228 0010 3 Chlamydia, gonorrhea and syphilis screening results documented (report when results are present for all of the 3 screenings) Gc chl syp documented
G9229 0010 3 Chlamydia, gonorrhea, and syphilis screening results not documented (patient refusal is the only allowed exception) Ptrsn no gc chl syp test
G9230 0010 3 Chlamydia, gonorrhea, and syphilis not screened, reason not given Norsn for gc chl syp test
G9231 0010 3 Documentation of end stage renal disease (esrd), dialysis, renal transplant before or during the measurement period or pregnancy during the measurement period Doc esrd dia trans preg
G9232 0010 3 Clinician treating major depressive disorder did not communicate to clinician treating comorbid condition for specified patient reason (e.g., patient is unable to communicate the diagnosis of a comorbid condition; the patient is unwilling to communicate the diagnosis of a comorbid condition; or the patient is unaware of the comorbid condition, or any other specified patient reason) Ptrsn no comm comorbid
G9233 0010 3 All quality actions for the applicable measures in the total knee replacement measures group have been performed for this patient Tkr composite
G9234 0010 3 I intend to report the total knee replacement measures group Tkr intent
G9235 0010 3 All quality actions for the applicable measures in the general surgery measures group have been performed for this patient Gs mg composite
G9236 0010 3 All quality actions for the applicable measures in the optimizing patient exposure to ionizing radiation measures group have been performed for this patient Op rad mg composite
G9237 0010 3 I intend to report the general surgery measures group Gs mg intent
G9238 0010 3 I intend to report the optimizing patient exposure to ionizing radiation measures group Op rad mg intent
G9239 0010 3 Documentation of reasons for patient initiating maintenance hemodialysis with a catheter as the mode of vascular access (e.g., patient has a maturing arteriovenous fistula (avf)/arteriovenous graft (avg), time-limited trial of hemodialysis, other medical reasons, patient declined avf/avg, other patient reasons, patient followed by reporting nephrologist for fewer than 90 days, other system reasons) Doc rsn hemod & cath acc
G9240 0010 3 Patient whose mode of vascular access is a catheter at the time maintenance hemodialysis is initiated Doc pt w cath maint dia
G9241 0010 3 Patient whose mode of vascular access is not a catheter at the time maintenance hemodialysis is initiated Doc pt w out cath maint dia
G9242 0010 3 Documentation of viral load equal to or greater than 200 copies/ml or viral load not performed Doc viral load >=200
G9243 0010 3 Documentation of viral load less than 200 copies/ml Doc viral load <200
G9244 0010 3 Antiretroviral thereapy not prescribed Antiviral not ordered
G9245 0010 3 Antiretroviral therapy prescribed Antiviral ordered
G9246 0010 3 Patient did not have at least one medical visit in each 6 month period of the 24 month measurement period, with a minimum of 60 days between medical visits No med visit in 24mo
G9247 0010 3 Patient had at least one medical visit in each 6 month period of the 24 month measurement period, with a minimum of 60 days between medical visits 1 med visit in 24mo
G9248 0010 3 Patient did not have a medical visit in the last 6 months No med visit 6mo
G9249 0010 3 Patient had a medical visit in the last 6 months Med visit w in 6mo
G9250 0010 3 Documentation of patient pain brought to a comfortable level within 48 hours from initial assessment Doc of pain comfort 48hr
G9251 0010 3 Documentation of patient with pain not brought to a comfortable level within 48 hours from initial assessment Doc no pain comfort 48hr
G9252 0010 3 Adenoma(s) or other neoplasm detected during screening colonoscopy Neo detect scrn colo
G9253 0010 3 Adenoma(s) or other neoplasm not detected during screening colonoscopy No neo detect scrn colo
G9254 0010 3 Documentation of patient discharged to home later than post-operative day 2 following cas Doc pt dischg >2d
G9255 0010 3 Documentation of patient discharged to home no later than post operative day 2 following cas Doc pt dischg <=2d
G9256 0010 3 Documentation of patient death following cas Doc of pat death after cas
G9257 0010 3 Documentation of patient stroke following cas Doc of pat stroke after cas
G9258 0010 3 Documentation of patient stroke following cea Doc of pat stroke after cea
G9259 0010 3 Documentation of patient survival and absence of stroke following cas Survive/no stroke post cas
G9260 0010 3 Documentation of patient death following cea Doc of pat death after cea
G9261 0010 3 Documentation of patient survival and absence of stroke following cea Survive/no stroke post cea
G9262 0010 3 Documentation of patient death in the hospital following endovascular aaa repair Doc of death post-aaa repair
G9263 0010 3 Documentation of patient discharged alive following endovascular aaa repair Doc of disch post-aaa repair
G9264 0010 3 Documentation of patient receiving maintenance hemodialysis for greater than or equal to 90 days with a catheter for documented reasons (e.g., other medical reasons, patient declined arteriovenous fistula (avf)/arteriovenous graft (avg), other patient reasons) Doc rsn hemod w/cath >=90d
G9265 0010 3 Patient receiving maintenance hemodialysis for greater than or equal to 90 days with a catheter as the mode of vascular access Doc cath >90d for maint dia
G9266 0010 3 Patient receiving maintenance hemodialysis for greater than or equal to 90 days without a catheter as the mode of vascular access Norsn pt cath >=90d
G9267 0010 3 Documentation of patient with one or more complications or mortality within 30 days Doc comp or mort w in 30d
G9268 0010 3 Documentation of patient with one or more complications within 90 days Doc comp or mort w in 90d
G9269 0010 3 Documentation of patient without one or more complications and without mortality within 30 days Doc no comp or mort w in 30d
G9270 0010 3 Documentation of patient without one or more complications within 90 days Doc no comp or mort w in 90d
G9271 0010 3 Ldl value < 100 Ldl under 100
G9272 0010 3 Ldl value >= 100 Ldl 100 and over
G9273 0010 3 Blood pressure has a systolic value of < 140 and a diastolic value of < 90 Sys<140 and dia<90
G9274 0010 3 Blood pressure has a systolic value of =140 and a diastolic value of = 90 or systolic value < 140 and diastolic value = 90 or systolic value = 140 and diastolic value < 90 Bp out of nrml limits
G9275 0010 3 Documentation that patient is a current non-tobacco user Doc of non tobacco user
G9276 0010 3 Documentation that patient is a current tobacco user Doc of tobacco user
G9277 0010 3 Documentation that the patient is on daily aspirin or anti-platelet or has documentation of a valid contraindication or exception to aspirin/anti-platelet; contraindications/exceptions include anti-coagulant use, allergy to aspirin or anti-platelets, history of gastrointestinal bleed and bleeding disorder; additionally, the following exceptions documented by the physician as a reason for not taking daily aspirin or anti-platelet are acceptable (use of non-steroidal anti-inflammatory agents, documented risk for drug interaction, uncontrolled hypertension defined as >180 systolic or >110 diastolic or gastroesophageal reflux) Doc daily aspirin or contra
G9278 0010 3 Documentation that the patient is not on daily aspirin or anti-platelet regimen Doc no daily aspirin
G9279 0010 3 Pneumococcal screening performed and documentation of vaccination received prior to discharge Pne scrn done doc vac done
G9280 0010 3 Pneumococcal vaccination not administered prior to discharge, reason not specified Pne not given norsn
G9281 0010 3 Screening performed and documentation that vaccination not indicated/patient refusal Pne scrn done doc not ind
G9282 0010 3 Documentation of medical reason(s) for not reporting the histological type or nsclc-nos classification with an explanation (e.g., biopsy taken for other purposes in a patient with a history of non-small cell lung cancer or other documented medical reasons) Doc medrsn no histo type
G9283 0010 3 Non small cell lung cancer biopsy and cytology specimen report documents classification into specific histologic type or classified as nsclc-nos with an explanation Hist type doc on report
G9284 0010 3 Non small cell lung cancer biopsy and cytology specimen report does not document classification into specific histologic type or classified as nsclc-nos with an explanation No hist type doc on report
G9285 0010 3 Specimen site other than anatomic location of lung or is not classified as non small cell lung cancer Site not small cell lung ca
G9286 0010 3 Antibiotic regimen prescribed within 10 days after onset of symptoms Antibio rx w in 10d of sympt
G9287 0010 3 Antibiotic regimen not prescribed within 10 days after onset of symptoms No antibio w in 10d of sympt
G9288 0010 3 Documentation of medical reason(s) for not reporting the histological type or nsclc-nos classification with an explanation (e.g., a solitary fibrous tumor in a person with a history of non-small cell carcinoma or other documented medical reasons) Doc medrsn no hist type rpt
G9289 0010 3 Non small cell lung cancer biopsy and cytology specimen report documents classification into specific histologic type or classified as nsclc-nos with an explanation Doc type nsm lung ca
G9290 0010 3 Non small cell lung cancer biopsy and cytology specimen report does not document classification into specific histologic type or classified as nsclc-nos with an explanation No doc type nsm lung ca
G9291 0010 3 Specimen site other than anatomic location of lung, is not classified as non small cell lung cancer or classified as nsclc-nos Not nsm lung ca
G9292 0010 3 Documentation of medical reason(s) for not reporting pt category and a statement on thickness and ulceration and for pt1, mitotic rate (e.g., negative skin biopsies in a patient with a history of melanoma or other documented medical reasons) Medrsn no pt category
G9293 0010 3 Pathology report does not include the pt category and a statement on thickness and ulceration and for pt1, mitotic rate No pt category on report
G9294 0010 3 Pathology report includes the pt category and a statement on thickness and ulceration and for pt1, mitotic rate Pt cat and thck on report
G9295 0010 3 Specimen site other than anatomic cutaneous location Non cutaneous loc
G9296 0010 3 Patients with documented shared decision-making including discussion of conservative (non-surgical) therapy (e.g., nsaids, analgesics, weight loss, exercise, injections) prior to the procedure Doc share dec prior proc
G9297 0010 3 Shared decision-making including discussion of conservative (non-surgical) therapy (e.g., nsaids, analgesics, weight loss, exercise, injections) prior to the procedure, not documented, reason not given No doc share dec prior proc
G9298 0010 3 Patients who are evaluated for venous thromboembolic and cardiovascular risk factors within 30 days prior to the procedure (e.g., history of dvt, pe, mi, arrhythmia and stroke) Eval risk vte card 30d prior
G9299 0010 3 Patients who are not evaluated for venous thromboembolic and cardiovascular risk factors within 30 days prior to the procedure including (e.g., history of dvt, pe, mi, arrhythmia and stroke, reason not given) No eval riskk vte card prior
G9300 0010 3 Documentation of medical reason(s) for not completely infusing the prophylactic antibiotic prior to the inflation of the proximal tourniquet (e.g., a tourniquet was not used) Doc medrsn no compl antibio
G9301 0010 3 Patients who had the prophylactic antibiotic completely infused prior to the inflation of the proximal tourniquet Doc compl inf antibio
G9302 0010 3 Prophylactic antibiotic not completely infused prior to the inflation of the proximal tourniquet, reason not given Norsn incomp inf antibio
G9303 0010 3 Operative report does not identify the prosthetic implant specifications including the prosthetic implant manufacturer, the brand name of the prosthetic implant and the size of each prosthetic implant, reason not given Norsn no pros info op rpt
G9304 0010 3 Operative report identifies the prosthetic implant specifications including the prosthetic implant manufacturer, the brand name of the prosthetic implant and the size of each prosthetic implant Pros info op rpt
G9305 0010 3 Intervention for presence of leak of endoluminal contents through an anastomosis not required No interv req for leak
G9306 0010 3 Intervention for presence of leak of endoluminal contents through an anastomosis required Interv req for leak
G9307 0010 3 No return to the operating room for a surgical procedure, for complications of the principal operative procedure, within 30 days of the principal operative procedure No ret for surg w in 30d
G9308 0010 3 Unplanned return to the operating room for a surgical procedure, for complications of the principal operative procedure, within 30 days of the principal operative procedure Unpl ret or w/compl w/in 30d
G9309 0010 3 No unplanned hospital readmission within 30 days of principal procedure No unplnd hosp readm in 30d
G9310 0010 3 Unplanned hospital readmission within 30 days of principal procedure Unplnd hosp readm in 30d
G9311 0010 3 No surgical site infection No surg site infection
G9312 0010 3 Surgical site infection Surgical site infection
G9313 0010 3 Amoxicillin, with or without clavulanate, not prescribed as first line antibiotic at the time of diagnosis for documented reason Amoxic not presc as 1st line
G9314 0010 3 Amoxicillin, with or without clavulanate, not prescribed as first line antibiotic at the time of diagnosis, reason not given Norsn not first line amox
G9315 0010 3 Documentation amoxicillin, with or without clavulanate, prescribed as a first line antibiotic at the time of diagnosis Doc first line amox
G9316 0010 3 Documentation of patient-specific risk assessment with a risk calculator based on multi-institutional clinical data, the specific risk calculator used, and communication of risk assessment from risk calculator with the patient or family Doc comm risk calc
G9317 0010 3 Documentation of patient-specific risk assessment with a risk calculator based on multi-institutional clinical data, the specific risk calculator used, and communication of risk assessment from risk calculator with the patient or family not completed No doc comm risk calc
G9318 0010 3 Imaging study named according to standardized nomenclature Image std nomenclature
G9319 0010 3 Imaging study not named according to standardized nomenclature, reason not given Image not std nomenclature
G9320 0010 3 Documentation of medical reason(s) for not naming ct studies according to a standardized nomenclature provided (eg, ct studies performed for radiation treatment planning or image-guided radiation treatment delivery) Medrsn no std nomenclature
G9321 0010 3 Count of previous ct (any type of ct) and cardiac nuclear medicine (myocardial perfusion) studies documented in the 12-month period prior to the current study Doc count of ct in 12mo
G9322 0010 3 Count of previous ct and cardiac nuclear medicine (myocardial perfusion) studies not documented in the 12-month period prior to the current study, reason not given No doc count of ct in 12mo
G9323 0010 3 Documentation of medical reason(s) for not counting previous ct and cardiac nuclear medicine (myocardial perfusion) studies (eg, ct studies performed for radiation treatment planning or image-guided radiation treatment delivery) Mdrsn no doc cnt of ct
G9324 0010 3 All necessary data elements not included, reason not given Not all data norsn
G9325 0010 3 Ct studies not reported to a radiation dose index registry due to medical reasons (eg, ct studies performed for radiation treatment planning or image-guided radiation treatment delivery) Medrsn no ct rpt to reg
G9326 0010 3 Ct studies performed not reported to a radiation dose index registry that is capable of collecting at a minimum all necessary data elements, reason not given Ct done no rad ds index, nrg
G9327 0010 3 Ct studies performed reported to a radiation dose index registry that is capable of collecting at a minimum all necessary data elements Ct done rad ds index
G9328 0010 3 Dicom format image data availability not documented in final report due to medical reasons (eg, ct studies performed for radiation treatment planning or image-guided radiation treatment delivery) Medrsn no dicom format doc
G9329 0010 3 Dicom format image data available to non-affiliated external healthcare facilities or entities on a secure, media free, reciprocally searchable basis with patient authorization for at least a 12-month period after the study not documented in final report, reason not given Norsn no dicom format doc
G9340 0010 3 Final report documented that dicom format image data available to non-affiliated external healthcare facilities or entities on a secure, media free, reciprocally searchable basis with patient authorization for at least a 12-month period after the study Dicom format doc on rpt
G9341 0010 3 Search conducted for prior patient ct studies completed at non-affiliated external healthcare facilities or entities within the past 12-months and are available through a secure, authorized, media-free, shared archive prior to an imaging study being performed Srch for ct w in 12 mos
G9342 0010 3 Search not conducted prior to an imaging study being performed for prior patient ct studies completed at non-affiliated external healthcare facilities or entities within the past 12-months and are available through a secure, authorized, media-free, shared archive, reason not given No srch for ct in 12mo norsn
G9343 0010 3 Due to medical reasons, search not conducted for dicom format images for prior patient ct imaging studies completed at non-affiliated external healthcare facilities or entities within the past 12 months that are available through a secure, authorized, media-free, shared archive (e.g., ct studies performed for radiation treatment planning or image-guided radiation treatment delivery) Medrsn no dicom srch
G9344 0010 3 Due to system reasons search not conducted for dicom format images for prior patient ct imaging studies completed at non-affiliated external healthcare facilities or entities within the past 12 months that are available through a secure, authorized, media-free, shared archive (e.g., non-affiliated external healthcare facilities or entities does not have archival abilities through a shared archival system) Sysrsn no dicom srch
G9345 0010 3 Follow-up recommendations documented according to recommended guidelines for incidentally detected pulmonary nodules (e.g., follow-up ct imaging studies needed or that no follow-up is needed) based at a minimum on nodule size and patient risk factors Follow up pulm nod
G9346 0010 3 Follow-up recommendations not documented according to recommended guidelines for incidentally detected pulmonary nodules due to medical reasons (e.g., patients with known malignant disease, patients with unexplained fever, ct studies performed for radiation treatment planning or image-guided radiation treatment delivery) No follow up pulm nod
G9347 0010 3 Follow-up recommendations not documented according to recommended guidelines for incidentally detected pulmonary nodules, reason not given No follow up pulm nod norsn
G9348 0010 3 Ct scan of the paranasal sinuses ordered at the time of diagnosis for documented reasons Doc rsn for ord ct scan
G9349 0010 3 Ct scan of the paranasal sinuses ordered at the time of diagnosis or received within 28 days after date of diagnosis Ct within 28 days
G9350 0010 3 Ct scan of the paranasal sinuses not ordered at the time of diagnosis or received within 28 days after date of diagnosis No doc sinus ct 28d or dx
G9351 0010 3 More than one ct scan of the paranasal sinuses ordered or received within 90 days after diagnosis Doc >1 sinus ct w 90d dx
G9352 0010 3 More than one ct scan of the paranasal sinuses ordered or received within 90 days after the date of diagnosis, reason not given Not >1 sinus ct w 90d dx
G9353 0010 3 More than one ct scan of the paranasal sinuses ordered or received within 90 days after the date of diagnosis for documented reasons (eg, patients with complications, second ct obtained prior to surgery, other medical reasons) Medrsn >1 sinus ct w 90d dx
G9354 0010 3 One ct scan or no ct scan of the paranasal sinuses ordered within 90 days after the date of diagnosis 1 or no ct sinus w/in 90d dx
G9355 0010 3 Early elective delivery or early induction not performed (less than 39 weeks gestation) No early ind/delivery
G9356 0010 3 Early elective delivery or early induction performed (less than 39 week gestation) Early ind/delivery
G9357 0010 3 Post-partum screenings, evaluations and education performed Pp eval/edu perf
G9358 0010 3 Post-partum screenings, evaluations and education not performed Pp eval/edu not perf
G9359 0010 3 Documentation of negative or managed positive tb screen with further evidence that tb is not active prior to the treatment with a biologic immune response modifier Neg mgd pos tb notact
G9360 0010 3 No documentation of negative or managed positive tb screen No doc of neg or man pos tb
G9361 0010 3 Medical indication for induction [documentation of reason(s) for elective delivery (c-section) or early induction (e.g., hemorrhage and placental complications, hypertension, preeclampsia and eclampsia, rupture of membranes-premature or prolonged, maternal conditions complicating pregnancy/delivery, fetal conditions complicating pregnancy/delivery, late pregnancy, prior uterine surgery, or participation in clinical trial)] Doc rsn elect c-sec/induct
G9362 0010 3 Duration of monitored anesthesia care (mac) or peripheral nerve block (pnb) without the use of general anesthesia during an applicable procedure 60 minutes or longer, as documented in the anesthesia record Mac or pnb w/o genanes >60m
G9363 0010 3 Duration of monitored anesthesia care (mac) or peripheral nerve block (pnb) without the use of general anesthesia during an applicable procedure or general or neuraxial anesthesia less than 60 minutes, as documented in the anesthesia record Mac or pnb w/o genanes <60m
G9364 0010 3 Sinusitis caused by, or presumed to be caused by, bacterial infection Sinus caus bac inx
G9365 0010 3 One high-risk medication ordered 1high risk med ord
G9366 0010 3 One high-risk medication not ordered 1high risk no ord
G9367 0010 3 At least two orders for the same high-risk medication >= 2 same hi-rsk med ord
G9368 0010 3 At least two orders for the same high-risk medications not ordered >= 2 same hi-rsk med not ord
G9369 0010 3 Individual filled at least two prescriptions for any antipsychotic medication and had a pdc of 0.8 or greater Fill 2 rx antipsych
G9370 0010 3 Individual who did not fill at least two prescriptions for any antipsychotic medication or did not have a pdc of 0.8 or greater Not fill 2 rx antipsych
G9376 0010 3 Patient continued to have the retina attached at the 6 months follow up visit (+/- 1 month) following only one surgery Contd ret attach at 6mth f/u
G9377 0010 3 Patient did not have the retina attached after 6 months following only one surgery No ret attach after 6mt
G9378 0010 3 Patient continued to have the retina attached at the 6 months follow up visit (+/- 1 month) Contd ret attach f/u vis
G9379 0010 3 Patient did not achieve flat retinas six months post surgery No acheive flat ret 6mth
G9380 0010 3 Patient offered assistance with end of life issues during the measurement period Off assis eol iss
G9381 0010 3 Documentation of medical reason(s) for not offering assistance with end of life issues (e.g., patient in hospice care, patient in terminal phase) during the measurement period Doc med reas no offer eol
G9382 0010 3 Patient not offered assistance with end of life issues during the measurement period No off assis eol
G9383 0010 3 Patient received screening for hcv infection within the 12 month reporting period Recd scrn hcv infec
G9384 0010 3 Documentation of medical reason(s) for not receiving annual screening for hcv infection (e.g., decompensated cirrhosis indicating advanced disease [i.e., ascites, esophageal variceal bleeding, hepatic encephalopathy], hepatocellular carcinoma, waitlist for organ transplant, limited life expectancy, other medical reasons) Doc med rsn no hcv scrn
G9385 0010 3 Documentation of patient reason(s) for not receiving annual screening for hcv infection (e.g., patient declined, other patient reasons) Doc pt reas not rec hcv srn
G9386 0010 3 Screening for hcv infection not received within the 12 month reporting period, reason not given Scrn hcv infec not recd
G9389 0010 3 Unplanned rupture of the posterior capsule requiring vitrectomy during cataract surgery Unpln rup post cap
G9390 0010 3 No unplanned rupture of the posterior capsule requiring vitrectomy during cataract surgery No unpln rup post cap
G9391 0010 3 Patient achieves refraction +-1 d for the eye that underwent cataract surgery, measured at the one month follow up visit Achv refrac +1d
G9392 0010 3 Patient does not achieve refraction +-1 d for the eye that underwent cataract surgery, measured at the one month follow up visit Not achv refrac +1d
G9393 0010 3 Patient with an initial phq-9 score greater than nine who achieves remission at twelve months as demonstrated by a twelve month (+/- 30 days) phq-9 score of less than five Ini phq9 >9 remiss <5
G9394 0010 3 Patient who had a diagnosis of bipolar disorder or personality disorder, death, permanent nursing home resident or receiving hospice or palliative care any time during the measurement or assessment period Dx bipol, death, nhres, hosp
G9395 0010 3 Patient with an initial phq-9 score greater than nine who did not achieve remission at twelve months as demonstrated by a twelve month (+/- 30 days) phq-9 score greater than or equal to five Ini phq9 >9 no remiss >=5
G9396 0010 3 Patient with an initial phq-9 score greater than nine who was not assessed for remission at twelve months (+/- 30 days) Ini phq9 >9 not assess
G9399 0010 3 Documentation in the patient record of a discussion between the physician/clinician and the patient that includes all of the following: treatment choices appropriate to genotype, risks and benefits, evidence of effectiveness, and patient preferences toward the outcome of the treatment Doc disc tx choices
G9400 0010 3 Documentation of medical or patient reason(s) for not discussing treatment options; medical reasons: patient is not a candidate for treatment due to advanced physical or mental health comorbidity (including active substance use); currently receiving antiviral treatment; successful antiviral treatment (with sustained virologic response) prior to reporting period; other documented medical reasons; patient reasons: patient unable or unwilling to participate in the discussion or other patient reasons Doc reas no disc tx opt
G9401 0010 3 No documentation of a discussion in the patient record of a discussion between the physician or other qualfied healthcare professional and the patient that includes all of the following: treatment choices appropriate to genotype, risks and benefits, evidence of effectiveness, and patient preferences toward treatment No disc tx choices
G9402 0010 3 Patient received follow-up on the date of discharge or within 30 days after discharge Recd f/u w/in 30d disch
G9403 0010 3 Clinician documented reason patient was not able to complete 30 day follow-up from acute inpatient setting discharge (e.g., patient death prior to follow-up visit, patient non-compliant for visit follow-up) Doc reas no 30 day f/u
G9404 0010 3 Patient did not receive follow-up on the date of discharge or within 30 days after discharge No 30 day f/u
G9405 0010 3 Patient received follow-up within 7 days after discharge Recd f/u w/in 7d dc
G9406 0010 3 Clinician documented reason patient was not able to complete 7 day follow-up from acute inpatient setting discharge (i.e patient death prior to follow-up visit, patient non-compliance for visit follow-up) Doc reas no 7d f/u
G9407 0010 3 Patient did not receive follow-up on or within 7 days after discharge No 7d f/u
G9408 0010 3 Patients with cardiac tamponade and/or pericardiocentesis occurring within 30 days Card tamp w/in 30d
G9409 0010 3 Patients without cardiac tamponade and/or pericardiocentesis occurring within 30 days No card tamp e/in 30d
G9410 0010 3 Patient admitted within 180 days, status post cied implantation, replacement, or revision with an infection requiring device removal or surgical revision Admit w/in 180d req remov
G9411 0010 3 Patient not admitted within 180 days, status post cied implantation, replacement, or revision with an infection requiring device removal or surgical revision No admit w/in 180d req remov
G9412 0010 3 Patient admitted within 180 days, status post cied implantation, replacement, or revision with an infection requiring device removal or surgical revision Admit w/in 180d req surg rev
G9413 0010 3 Patient not admitted within 180 days, status post cied implantation, replacement, or revision with an infection requiring device removal or surgical revision No admit req surg rev
G9414 0010 3 Patient had one dose of meningococcal vaccine (serogroups a, c, w, y) on or between the patient’s 11th and 13th birthdays 1dose menig vac btwn 11 & 13
G9415 0010 3 Patient did not have one dose of meningococcal vaccine on or between the patient’s 11th and 13th birthdays No 1dose meni vac btwn 11&13
G9416 0010 3 Patient had one tetanus, diphtheria toxoids and acellular pertussis vaccine (tdap) on or between the patient’s 10th and 13th birthdays Pt 1 tdap betw 10-13 yrs
G9417 0010 3 Patient did not have one tetanus, diphtheria toxoids and acellular pertussis vaccine (tdap) on or between the patient’s 10th and 13th birthdays Pt not 1 tdap betw 10-13 yrs
G9418 0010 3 Primary non-small cell lung cancer biopsy and cytology specimen report documents classification into specific histologic type or classified as nsclc-nos with an explanation Lungcx bx rpt docs class
G9419 0010 3 Documentation of medical reason(s) for not including the histological type or nsclc-nos classification with an explanation (e.g., biopsy taken for other purposes in a patient with a history of primary non-small cell lung cancer or other documented medical reasons) Med reas not incl histo type
G9420 0010 3 Specimen site other than anatomic location of lung or is not classified as primary non-small cell lung cancer Spec site no lung
G9421 0010 3 Primary non-small cell lung cancer biopsy and cytology specimen report does not document classification into specific histologic type or classified as nsclc-nos with an explanation Lung cx bx rpt no doc class
G9422 0010 3 Primary lung carcinoma resection report documents pt category, pn category and for non-small cell lung cancer, histologic type (squamous cell carcinoma, adenocarcinoma and not nsclc-nos) Rpt doc class histo type
G9423 0010 3 Documentation of medical reason for not including pt category, pn category and histologic type [for patient with appropriate exclusion criteria (e.g., metastatic disease, benign tumors, malignant tumors other than carcinomas, inadequate surgical specimens)] Med reas rpt no histo type
G9424 0010 3 Specimen site other than anatomic location of lung, or classified as nsclc-nos Site no lung or lung cx
G9425 0010 3 Primary lung carcinoma resection report does not document pt category, pn category and for non-small cell lung cancer, histologic type (squamous cell carcinoma, adenocarcinoma) Spec rpt no doc class histo
G9426 0010 3 Improvement in median time from ed arrival to initial ed oral or parenteral pain medication administration performed for ed admitted patients Impr med time edarr pain med
G9427 0010 3 Improvement in median time from ed arrival to initial ed oral or parenteral pain medication administration not performed for ed admitted patients No impro med time pain med
G9428 0010 3 Pathology report includes the pt category and a statement on thickness, ulceration and mitotic rate Patho rpt incl pt ctg
G9429 0010 3 Documentation of medical reason(s) for not including pt category and a statement on thickness, ulceration and mitotic rate (e.g., negative skin biopsies in a patient with a history of melanoma or other documented medical reasons) Doc med rsn no pt cat
G9430 0010 3 Specimen site other than anatomic cutaneous location Spec site no cutaneous
G9431 0010 3 Pathology report does not include the pt category and a statement on thickness, ulceration and mitotic rate Patho rpt no pt ctg
G9432 0010 3 Asthma well-controlled based on the act, c-act, acq, or ataq score and results documented Asth controlled
G9433 0010 3 Death, permanent nursing home resident or receiving hospice or palliative care any time during the measurement period Death, nhres, hospice
G9434 0010 3 Asthma not well-controlled based on the act, c-act, acq, or ataq score, or specified asthma control tool not used, reason not given Asth not controlled
G9435 0010 3 Aspirin prescribed at discharge Asp presc disch
G9436 0010 3 Aspirin not prescribed for documented reasons (e.g., allergy, medical intolerance, history of bleed) Asp not presc doc reas
G9437 0010 3 Aspirin not prescribed at discharge Asp not presc disch
G9438 0010 3 P2y inhibitor prescribed at discharge P2y inhib presc
G9439 0010 3 P2y inhibitor not prescribed for documented reasons (e.g., allergy, medical intolerance, history of bleed) P2y inhib not presc doc reas
G9440 0010 3 P2y inhibitor not prescribed at discharge P2y inhib not presc
G9441 0010 3 Statin prescribed at discharge Statin presc disch
G9442 0010 3 Statin not prescribed for documented reasons (e.g., allergy, medical intolerance) Statin not presc doc reas
G9443 0010 3 Statin not prescribed at discharge Statin not presc disch
G9448 0010 3 Patients who were born in the years 1945?1965 Born 1945-1965
G9449 0010 3 History of receiving blood transfusions prior to 1992 Hx bld transf b/f 1992
G9450 0010 3 History of injection drug use Hx injec drug use
G9451 0010 3 Patient received one-time screening for hcv infection 1x scrn hcv infect
G9452 0010 3 Documentation of medical reason(s) for not receiving one-time screening for hcv infection (e.g., decompensated cirrhosis indicating advanced disease [ie, ascites, esophageal variceal bleeding, hepatic encephalopathy], hepatocellular carcinoma, waitlist for organ transplant, limited life expectancy, other medical reasons) Doc med reas no scrn hcv
G9453 0010 3 Documentation of patient reason(s) for not receiving one-time screening for hcv infection (e.g., patient declined, other patient reasons) Pt reas no hcv infect
G9454 0010 3 One-time screening for hcv infection not received within 12-month reporting period and no documentation of prior screening for hcv infection, reason not given No scr hcv inf 12 mth rp
G9455 0010 3 Patient underwent abdominal imaging with ultrasound, contrast enhanced ct or contrast mri for hcc Abd imag w/us, ct or mri
G9456 0010 3 Documentation of medical or patient reason(s) for not ordering or performing screening for hcc. medical reason: comorbid medical conditions with expected survival < 5 years, hepatic decompensation and not a candidate for liver transplantation, or other medical reasons; patient reasons: patient declined or other patient reasons (e.g., cost of tests, time related to accessing testing equipment) Doc med pt reas no hcc scrn
G9457 0010 3 Patient did not undergo abdominal imaging and did not have a documented reason for not undergoing abdominal imaging in the submission period Pt no abd img no doc rsn
G9458 0010 3 Patient documented as tobacco user and received tobacco cessation intervention (must include at least one of the following: advice given to quit smoking or tobacco use, counseling on the benefits of quitting smoking or tobacco use, assistance with or referral to external smoking or tobacco cessation support programs, or current enrollment in smoking or tobacco use cessation program) if identified as a tobacco user Tob user recd cess interv
G9459 0010 3 Currently a tobacco non-user Tob non-user
G9460 0010 3 Tobacco assessment or tobacco cessation intervention not performed, reason not given No tob assess or cess inter
G9463 0010 3 I intend to report the sinusitis measures group Sinusitis intent
G9464 0010 3 All quality actions for the applicable measures in the sinusitis measures group have been performed for this patient Sinusitis comp
G9465 0010 3 I intend to report the acute otitis externa (aoe) measures group Aoe intent
G9466 0010 3 All quality actions for the applicable measures in the aoe measures group have been performed for this patient Aoe comp
G9467 0010 3 Patient who have received or are receiving corticosteroids greater than or equal to 10 mg/day of prednisone equivalents for 60 or greater consecutive days or a single prescription equating to 600 mg prednisone or greater for all fills within the last twelve months Recd cortico >=10mg/day >60d
G9468 0010 3 Patient not receiving corticosteroids greater than or equal to 10 mg/day of prednisone equivalents for 60 or greater consecutive days or a single prescription equating to 600 mg prednisone or greater for all fills No recd cortico>=10mg/d >60d
G9469 0010 3 Patients who have received or are receiving corticosteroids greater than or equal to 10 mg/day of prednisone equivalents for 90 or greater consecutive days or a single prescription equating to 900 mg prednisone or greater for all fills Rec cortico>90d or 1rx 900mg
G9470 0010 3 Patients not receiving corticosteroids greater than or equal to 10 mg/day of prednisone equivalents for 60 or greater consecutive days or a single prescription equating to 600 mg prednisone or greater for all fills No rec cortico>60d 1rx 600mg
G9471 0010 3 Within the past 2 years, central dual-energy x-ray absorptiometry (dxa) not ordered or documented W/in 2yr dxa not order
G9472 0010 3 Within the past 2 years, central dual-energy x-ray absorptiometry (dxa) not ordered and documented, no review of systems and no medication history or pharmacologic therapy (other than minerals/vitamins) for osteoporosis prescribed No dxa no med hx no rv sx
G9473 0010 3 Services performed by chaplain in the hospice setting, each 15 minutes Chap services at hospice
G9474 0010 3 Services performed by dietary counselor in the hospice setting, each 15 minutes Diet counsel at hospice
G9475 0010 3 Services performed by other counselor in the hospice setting, each 15 minutes Other counselor at hospice
G9476 0010 3 Services performed by volunteer in the hospice setting, each 15 minutes Volun service at hospice
G9477 0010 3 Services performed by care coordinator in the hospice setting, each 15 minutes Care coord at hospice
G9478 0010 3 Services performed by other qualified therapist in the hospice setting, each 15 minutes Othe therapist at hospice
G9479 0010 3 Services performed by qualified pharmacist in the hospice setting, each 15 minutes Pharmacist at hospice
G9480 0010 3 Admission to medicare care choice model program (mccm) Admission to mccm
G9481 0010 3 Remote in-home visit for the evaluation and management of a new patient for use only in a medicare-approved cms innovation center demonstration project, which requires these 3 key components: a problem focused history; a problem focused examination; and straightforward medical decision making, furnished in real time using interactive audio and video technology. counseling and coordination of care with other physicians, other qualified health care professionals or agencies are provided consistent with the nature of the problem(s) and the needs of the patient or the family or both. usually, the presenting problem(s) are self limited or minor. typically, 10 minutes are spent with the patient or family or both via real time, audio and video intercommunications technology Remote e/m new pt 10mins
G9482 0010 3 Remote in-home visit for the evaluation and management of a new patient for use only in a medicare-approved cms innovation center demonstration project, which requires these 3 key components: an expanded problem focused history; an expanded problem focused examination; straightforward medical decision making, furnished in real time using interactive audio and video technology. counseling and coordination of care with other physicians, other qualified health care professionals or agencies are provided consistent with the nature of the problem(s) and the needs of the patient or the family or both. usually, the presenting problem(s) are of low to moderate severity. typically, 20 minutes are spent with the patient or family or both via real time, audio and video intercommunications technology Remote e/m new pt 20mins
G9483 0010 3 Remote in-home visit for the evaluation and management of a new patient for use only in a medicare-approved cms innovation center demonstration project, which requires these 3 key components: a detailed history; a detailed examination; medical decision making of low complexity, furnished in real time using interactive audio and video technology. counseling and coordination of care with other physicians, other qualified health care professionals or agencies are provided consistent with the nature of the problem(s) and the needs of the patient or the family or both. usually, the presenting problem(s) are of moderate severity. typically, 30 minutes are spent with the patient or family or both via real time, audio and video intercommunications technology Remote e/m new pt 30mins
G9484 0010 3 Remote in-home visit for the evaluation and management of a new patient for use only in a medicare-approved cms innovation center demonstration project, which requires these 3 key components: a comprehensive history; a comprehensive examination; medical decision making of moderate complexity, furnished in real time using interactive audio and video technology. counseling and coordination of care with other physicians, other qualified health care professionals or agencies are provided consistent with the nature of the problem(s) and the needs of the patient or the family or both. usually, the presenting problem(s) are of moderate to high severity. typically, 45 minutes are spent with the patient or family or both via real time, audio and video intercommunications technology Remote e/m new pt 45mins
G9485 0010 3 Remote in-home visit for the evaluation and management of a new patient for use only in a medicare-approved cms innovation center demonstration project, which requires these 3 key components: a comprehensive history; a comprehensive examination; medical decision making of high complexity, furnished in real time using interactive audio and video technology. counseling and coordination of care with other physicians, other qualified health care professionals or agencies are provided consistent with the nature of the problem(s) and the needs of the patient or the family or both. usually, the presenting problem(s) are of moderate to high severity. typically, 60 minutes are spent with the patient or family or both via real time, audio and video intercommunications technology Remote e/m new pt 60mins
G9486 0010 3 Remote in-home visit for the evaluation and management of an established patient for use only in a medicare-approved cms innovation center demonstration project, which requires at least 2 of the following 3 key components: a problem focused history; a problem focused examination; straightforward medical decision making, furnished in real time using interactive audio and video technology. counseling and coordination of care with other physicians, other qualified health care professionals or agencies are provided consistent with the nature of the problem(s) and the needs of the patient or the family or both. usually, the presenting problem(s) are self limited or minor. typically, 10 minutes are spent with the patient or family or both via real time, audio and video intercommunications technology Remote e/m est. pt 10mins
G9487 0010 3 Remote in-home visit for the evaluation and management of an established patient for use only in a medicare-approved cms innovation center demonstration project, which requires at least 2 of the following 3 key components: an expanded problem focused history; an expanded problem focused examination; medical decision making of low complexity, furnished in real time using interactive audio and video technology. counseling and coordination of care with other physicians, other qualified health care professionals or agencies are provided consistent with the nature of the problem(s) and the needs of the patient or the family or both. usually, the presenting problem(s) are of low to moderate severity. typically, 15 minutes are spent with the patient or family or both via real time, audio and video intercommunications technology Remote e/m est. pt 15mins
G9488 0010 3 Remote in-home visit for the evaluation and management of an established patient for use only in a medicare-approved cms innovation center demonstration project, which requires at least 2 of the following 3 key components: a detailed history; a detailed examination; medical decision making of moderate complexity, furnished in real time using interactive audio and video technology. counseling and coordination of care with other physicians, other qualified health care professionals or agencies are provided consistent with the nature of the problem(s) and the needs of the patient or the family or both. usually, the presenting problem(s) are of moderate to high severity. typically, 25 minutes are spent with the patient or family or both via real time, audio and video intercommunications technology Remote e/m est. pt 25mins
G9489 0010 3 Remote in-home visit for the evaluation and management of an established patient for use only in a medicare-approved coms innovation center demonstration project, which requires at least 2 of the following 3 key components: a comprehensive history; a comprehensive examination; medical decision making of high complexity, furnished in real time using interactive audio and video technology. counseling and coordination of care with other physicians, other qualified health care professionals or agencies are provided consistent with the nature of the problem(s) and the needs of the patient or the family or both. usually, the presenting problem(s) are of moderate to high severity. typically, 40 minutes are spent with the patient or family or both via real time, audio and video intercommunications technology Remote e/m est. pt 40mins
G9490 0010 3 Cms innovation center models, home visit for patient assessment performed by clinical staff for an individual not considered homebound, including, but not necessarily limited to patient assessment of clinical status, safety/fall prevention, functional status/ambulation, medication reconciliation/management, compliance with orders/plan of care, performance of activities of daily living, and ensuring beneficiary connections to community and other services. (for use only in medicare-approved cms innovation center models); may not be billed for a 30 day period covered by a transitional care management code Cmmi mod home visit
G9496 0010 3 Documentation of reason for not detecting adenoma(s) or other neoplasm. (e.g., neoplasm detected is only diagnosed as traditional serrated adenoma, sessile serrated polyp, or sessile serrated adenoma Doc rsn no adeno/neopl detec
G9497 0010 3 Received instruction from the anesthesiologist or proxy prior to the day of surgery to abstain from smoking on the day of surgery Rec inst no smoke day surg
G9498 0010 3 Antibiotic regimen prescribed Abx reg prescribed
G9499 0010 3 Patient did not start or is not receiving antiviral treatment for hepatitis c during the measurement period No start/rec antvir tx hep c
G9500 0010 3 Radiation exposure indices, or exposure time and number of fluorographic images in final report for procedures using fluoroscopy, documented Rad expos ind/exp tm doc
G9501 0010 3 Radiation exposure indices, or exposure time and number of fluorographic images not documented in final report for procedure using fluoroscopy, reason not given Rad expos ind/exp tm no doc
G9502 0010 3 Documentation of medical reason for not performing foot exam (i.e., patients who have had either a bilateral amputation above or below the knee, or both a left and right amputation above or below the knee before or during the measurement period) Med reas no perf foot exam
G9503 0010 3 Patient taking tamsulosin hydrochloride Pt tk tams hcl
G9504 0010 3 Documented reason for not assessing hepatitis b virus (hbv) status (e.g., patient not initiating anti-tnf therapy, patient declined) prior to initiating anti-tnf therapy Doc rsn hep b stat not asses
G9505 0010 3 Antibiotic regimen prescribed within 10 days after onset of symptoms for documented medical reason Abx pres w/in 10 dys of symp
G9506 0010 3 Biologic immune response modifier prescribed Bio imm resp mod presc
G9507 0010 3 Documentation that the patient is on a statin medication or has documentation of a valid contraindication or exception to statin medications; contraindications/exceptions that can be defined by diagnosis codes include pregnancy during the measurement period, active liver disease, rhabdomyolysis, end stage renal disease on dialysis and heart failure; provider documented contraindications/exceptions include breastfeeding during the measurement period, woman of child-bearing age not actively taking birth control, allergy to statin, drug interaction (hiv protease inhibitors, nefazodone, cyclosporine, gemfibrozil, and danazol) and intolerance (with supporting documentation of trying a statin at least once within the last 5 years or diagnosis codes for myostitis or toxic myopathy related to drugs) Doc reas on statin or contra
G9508 0010 3 Documentation that the patient is not on a statin medication Doc pt not on statin
G9509 0010 3 Adult patients 18 years of age or older with major depression or dysthymia who reached remission at twelve months as demonstrated by a twelve month (+/-60 days) phq-9 or phq-9m score of less than 5 Adit mdd dys rem 12 mnths
G9510 0010 3 Adult patients 18 years of age or older with major depression or dysthymia who did not reach remission at twelve months as demonstrated by a twelve month (+/-60 days) phq-9 or phq-9m score of less than 5. either phq- 9 or phq-9m score was not assessed or is greater than or equal to 5 Remis12m not phq-9 score <5
G9511 0010 3 Index event date phq-9 or phq-9m score greater than 9 documented during the twelve month denominator identification period Idx evt dte phq>9 doc 12 mo
G9512 0010 3 Individual had a pdc of 0.8 or greater Indiv pdc > 0.8
G9513 0010 3 Individual did not have a pdc of 0.8 or greater Indiv pdc not > 0.8
G9514 0010 3 Patient required a return to the operating room within 90 days of surgery Req ret or w/in 90d of surg
G9515 0010 3 Patient did not require a return to the operating room within 90 days of surgery No reas, no ret or w/in 90d
G9516 0010 3 Patient achieved an improvement in visual acuity, from their preoperative level, within 90 days of surgery Impr vis acuit w/in 90d
G9517 0010 3 Patient did not achieve an improvement in visual acuity, from their preoperative level, within 90 days of surgery, reason not given No impr vis acuit w/in 90d
G9518 0010 3 Documentation of active injection drug use Doc active inj drug use
G9519 0010 3 Patient achieves final refraction (spherical equivalent) +/- 1.0 diopters of their planned refraction within 90 days of surgery Final ref +/- 1.0 w/in 90d
G9520 0010 3 Patient does not achieve final refraction (spherical equivalent) +/- 1.0 diopters of their planned refraction within 90 days of surgery Refract not +/- 1.0 w/in 90d
G9521 0010 3 Total number of emergency department visits and inpatient hospitalizations less than two in the past 12 months Er and ip hosp <2 in 12 mos
G9522 0010 3 Total number of emergency department visits and inpatient hospitalizations equal to or greater than two in the past 12 months or patient not screened, reason not given Er/ip hosp =/>2 in 12 mos
G9523 0010 3 Patient discontinued from hemodialysis or peritoneal dialysis D/c hemo or perit dialysis
G9524 0010 3 Patient was referred to hospice care Refer to hospice
G9525 0010 3 Documentation of patient reason(s) for not referring to hospice care (e.g., patient declined, other patient reasons) Doc pt reas no hospice refer
G9526 0010 3 Patient was not referred to hospice care, reason not given No reason, no refer hospice
G9529 0010 3 Patient with minor blunt head trauma had an appropriate indication(s) for a head ct Minor blunt trauma w/head ct
G9530 0010 3 Patient presented with a minor blunt head trauma and had a head ct ordered for trauma by an emergency care provider Pt mbht hd ct ord ec prov
G9531 0010 3 Patient has documentation of ventricular shunt, brain tumor, multisystem trauma, or is currently taking an antiplatelet medication including: abciximab, anagrelide, cangrelor, cilostazol, clopidogrel, dipyridamole, eptifibatide, prasugrel, ticlopidine, ticagrelor, tirofiban, or vorapaxar Pt doc
G9532 0010 3 Patient had a head ct for trauma ordered by someone other than an emergency care provider or was ordered for a reason other than trauma Pt hd ct ord
G9533 0010 3 Patient with minor blunt head trauma did not have an appropriate indication(s) for a head ct Indic for head ct not valid
G9534 0010 3 Advanced brain imaging (cta, ct, mra or mri) was not ordered Adv brain image not ordered
G9535 0010 3 Patients with a normal neurological examination Normal neuro exam
G9536 0010 3 Documentation of medical reason(s) for ordering an advanced brain imaging study (i.e., patient has an abnormal neurological examination; patient has the coexistence of seizures, or both; recent onset of severe headache; change in the type of headache; signs of increased intracranial pressure (e.g., papilledema, absent venous pulsations on funduscopic examination, altered mental status, focal neurologic deficits, signs of meningeal irritation); hiv-positive patients with a new type of headache; immunocompromised patient with unexplained headache symptoms; patient on coagulopathy/anti-coagulation or anti-platelet therapy; very young patients with unexplained headache symptoms) Doc med reas adv brain image
G9537 0010 3 Documentation of system reason(s) for obtaining imaging of the head (ct or mri) (i.e., needed as part of a clinical trial; other clinician ordered the study) Doc sysm rsn img hd
G9538 0010 3 Advanced brain imaging (cta, ct, mra or mri) was ordered Adv brain image ordered
G9539 0010 3 Intent for potential removal at time of placement Intent pot remv time placemt
G9540 0010 3 Patient alive 3 months post procedure Pt alive 3 mos post proc
G9541 0010 3 Filter removed within 3 months of placement Filter rem 3 mon plmt
G9542 0010 3 Documented re-assessment for the appropriateness of filter removal within 3 months of placement Doc reass appr remo filt 3ms
G9543 0010 3 Documentation of at least two attempts to reach the patient to arrange a clinical re-assessment for the appropriateness of filter removal within 3 months of placement Doc 2x re-assess filt remov
G9544 0010 3 Patients that do not have the filter removed, documented re-assessment for the appropriateness of filter removal, or documentation of at least two attempts to reach the patient to arrange a clinical re-assessment for the appropriateness of filter removal within 3 months of placement No filt remov w/in 3mos plcm
G9547 0010 3 Cystic renal lesion that is simple appearing (bosniak i or ii) , or adrenal lesion less than or equal to 1.0 cm or adrenal lesion greater than 1.0 cm but less than or equal to 4.0 cm classified as likely benign by unenhanced ct or washout protocol ct, or mri with in- and opposed-phase sequences or other equivalent institutional imaging protocols Cys ren les or adren
G9548 0010 3 Final reports for imaging studies stating no follow-up imaging is recommended No f/u rec image study
G9549 0010 3 Documentation of medical reason(s) that follow-up imaging is indicated (e.g., patient has lymphadenopathy, signs of metastasis or an active diagnosis or history of cancer, and other medical reason(s)) Doc med rsn for f/u imag
G9550 0010 3 Final reports for imaging studies with follow-up imaging recommended Imag rec
G9551 0010 3 Final reports for imaging studies without an incidentally found lesion noted Imag no les
G9552 0010 3 Incidental thyroid nodule < 1.0 cm noted in report Inc thyr node <1.0 in rpt
G9553 0010 3 Prior thyroid disease diagnosis Prior thyroid dise dx
G9554 0010 3 Final reports for ct, cta, mri or mra of the chest or neck or ultrasound of the neck with follow-up imaging recommended Ct/cta/mri/a chst foll rec
G9555 0010 3 Documentation of medical reason(s) for recommending follow up imaging (e.g., patient has multiple endocrine neoplasia, patient has cervical lymphadenopathy, other medical reason(s)) Doc med rsn for follup image
G9556 0010 3 Final reports for ct, cta, mri or mra of the chest or neck or ultrasound of the neck with follow-up imaging not recommended Ct/cta/mri/a no follup imag
G9557 0010 3 Final reports for ct, cta, mri or mra studies of the chest or neck or ultrasound of the neck without an incidentally found thyroid nodule < 1.0 cm noted or no nodule found Ct/cta/mri/a no thyr <1.0cm
G9558 0010 3 Patient treated with a beta-lactam antibiotic as definitive therapy Tx beta-lactam abx therapy
G9559 0010 3 Documentation of medical reason(s) for not prescribing a beta-lactam antibiotic (e.g., allergy, intolerance to beta-lactam antibiotics) Doc med reas no abx therapy
G9560 0010 3 Patient not treated with a beta-lactam antibiotic as definitive therapy, reason not given No beta-lactam abx ther, rng
G9561 0010 3 Patients prescribed opiates for longer than six weeks Presc opiates >6 wks
G9562 0010 3 Patients who had a follow-up evaluation conducted at least every three months during opioid therapy Foll-up eval q3mo opiod tx
G9563 0010 3 Patients who did not have a follow-up evaluation conducted at least every three months during opioid therapy No f/u eval q3mo opiod tx
G9572 0010 3 Index date phq-score greater than 9 documented during the twelve month denominator identification period Phq-scr >9 doc in 12m time
G9573 0010 3 Adult patients 18 years of age or older with major depression or dysthymia who did not reach remission at six months as demonstrated by a six month (+/-60 days) phq-9 or phq-9m score of less than five Adl pt md or dys rem 6 mon
G9574 0010 3 Adult patients 18 years of age or older with major depression or dysthymia who did not reach remission at six months as demonstrated by a six month (+/-60 days) phq-9 or phq-9m score of less than five; either phq-9 or phq-9m score was not assessed or is greater than or equal to five Adl pt md dys no rem 6 mon
G9577 0010 3 Patients prescribed opiates for longer than six weeks Presc opiates >6 wks
G9578 0010 3 Documentation of signed opioid treatment agreement at least once during opioid therapy Doc opioid tx 1x during ther
G9579 0010 3 No documentation of signed an opioid treatment agreement at least once during opioid therapy No doc opioid tx 1x at ther
G9580 0010 3 Door to puncture time of less than 2 hours Door to punc time <2hrs
G9581 0010 3 Door to puncture time of greater than 2 hours for reasons documented by clinician (e.g., patients who are transferred from one institution to another with a known diagnosis of cva for endovascular stroke treatment; hospitalized patients with newly diagnosed cva considered for endovascular stroke treatment) Md doc, door to punc tm >2hr
G9582 0010 3 Door to puncture time of greater than 2 hours, no reason given Door to punc time >2hr, nrg
G9583 0010 3 Patients prescribed opiates for longer than six weeks Presc opiates >6 wks
G9584 0010 3 Patient evaluated for risk of misuse of opiates by using a brief validated instrument (e.g., opioid risk tool, soapp-r) or patient interviewed at least once during opioid therapy Eval opioid use instr/pt int
G9585 0010 3 Patient not evaluated for risk of misuse of opiates by using a brief validated instrument (e.g., opioid risk tool, soapp-r) or patient not interviewed at least once during opioid therapy No eval opi use instr/intv
G9593 0010 3 Pediatric patient with minor blunt head trauma classified as low risk according to the pecarn prediction rules Low pecarn ped head trauma
G9594 0010 3 Patient presented with a minor blunt head trauma and had a head ct ordered for trauma by an emergency care provider Pt mbht hd ct ord ec prov
G9595 0010 3 Patient has documentation of ventricular shunt, brain tumor, or coagulopathy Doc shnt/tum/coag
G9596 0010 3 Pediatric patient had a head ct for trauma ordered by someone other than an emergency care provider or was ordered for a reason other than trauma Ped pt hd ct ord
G9597 0010 3 Pediatric patient with minor blunt head trauma not classified as low risk according to the pecarn prediction rules No low pecarn ped head traum
G9598 0010 3 Aortic aneurysm 5.5 - 5.9 cm maximum diameter on centerline formatted ct or minor diameter on axial formatted ct Aor ane 5.5-5.9 cm max diam
G9599 0010 3 Aortic aneurysm 6.0 cm or greater maximum diameter on centerline formatted ct or minor diameter on axial formatted ct Aor ane >=6.0 cm max diam
G9600 0010 3 Symptomatic aaas that required urgent/emergent (non-elective) repair Symp aaa urgent repair
G9601 0010 3 Patient discharge to home no later than post-operative day #7 Pt dchg home post op day 7
G9602 0010 3 Patient not discharged to home by post-operative day #7 Pt no dchg home postop day 7
G9603 0010 3 Patient survey score improved from baseline following treatment Pt surv improv bsline tx
G9604 0010 3 Patient survey results not available Pt surv results not avail
G9605 0010 3 Patient survey score did not improve from baseline following treatment Surv score no improv w/tx
G9606 0010 3 Intraoperative cystoscopy performed to evaluate for lower tract injury Intraop cyst eval trac inj
G9607 0010 3 Documented medical reasons for not performing intraoperative cystoscopy (e.g., urethral pathology precluding cystoscopy, any patient who has a congenital or acquired absence of the urethra) or in the case of patient death Doc med rsn not perf cystosc
G9608 0010 3 Intraoperative cystoscopy not performed to evaluate for lower tract injury Intraop cyst eval not done
G9609 0010 3 Documentation of an order for anti-platelet agents Doc order anti-plat
G9610 0010 3 Documentation of medical reason(s) in the patient’s record for not ordering anti-platelet agents Doc md rsn no antipla
G9611 0010 3 Order for anti-platelet agents was not documented in the patient’s record, reason not given No doc order anti-plat rng
G9612 0010 3 Photodocumentation of two or more cecal landmarks to establish a complete examination Phodoc 2 mr cec lndmk
G9613 0010 3 Documentation of post-surgical anatomy (e.g., right hemicolectomy, ileocecal resection, etc.) Doc post surg anatomy
G9614 0010 3 Photodocumentation of less than two cecal landmarks (i.e., no cecal landmarks or only one cecal landmark) to establish a complete examination Photodoc < 2 cec lndmk
G9615 0010 3 Preoperative assessment documented Pre-op asst doc
G9616 0010 3 Documentation of reason(s) for not documenting a preoperative assessment (e.g., patient with a gynecologic or other pelvic malignancy noted at the time of surgery) Doc rsn no preop assmt
G9617 0010 3 Preoperative assessment not documented, reason not given Pre-op asst not doc, rng
G9618 0010 3 Documentation of screening for uterine malignancy or those that had an ultrasound and/or endometrial sampling of any kind Doc scr uter mal or us/samp
G9619 0010 3 Documentation of reason(s) for not screening for uterine malignancy (e.g., prior hysterectomy) Doc rsn no scr uter malig
G9620 0010 3 Patient not screened for uterine malignancy, or those that have not had an ultrasound and/or endometrial sampling of any kind, reason not given No scr utr malig/us/samp rng
G9621 0010 3 Patient identified as an unhealthy alcohol user when screened for unhealthy alcohol use using a systematic screening method and received brief counseling Scr unheal etoh w/counsel
G9622 0010 3 Patient not identified as an unhealthy alcohol user when screened for unhealthy alcohol use using a systematic screening method No unheal etoh user
G9623 0010 3 Documentation of medical reason(s) for not screening for unhealthy alcohol use (e.g., limited life expectancy, other medical reasons) Doc med rsn no scr etoh use
G9624 0010 3 Patient not screened for unhealthy alcohol use using a systematic screening method or patient did not receive brief counseling if identified as an unhealthy alcohol user, reason not given Pt not scrn or no counseling
G9625 0010 3 Patient sustained bladder injury at the time of surgery or discovered subsequently up to 30 days post-surgery Pt bl srg 30 day pst srg
G9626 0010 3 Documented medical reason for not reporting bladder injury (e.g., gynecologic or other pelvic malignancy documented, concurrent surgery involving bladder pathology, injury that occurs during urinary incontinence procedure, patient death from non-medical causes not related to surgery, patient died during procedure without evidence of bladder injury) Med rsn no rpt baldder inj
G9627 0010 3 Patient did not sustain bladder injury at the time of surgery nor discovered subsequently up to 30n days post-surgery Pt no bl srg 30 day pst srg
G9628 0010 3 Patient sustained bowel injury at the time of surgery or discovered subsequently up to 30 days post-surgery Pt bwli srg 30 day pst srg
G9629 0010 3 Documented medical reasons for not reporting bowel injury (e.g., gynecologic or other pelvic malignancy documented, planned (e.g., not due to an unexpected bowel injury) resection and/or re-anastomosis of bowel, or patient death from non-medical causes not related to surgery, patient died during procedure without evidence of bowel injury) Med rsn no rpt bowel inj
G9630 0010 3 Patient did not sustain a bowel injury at the time of surgery nor discovered subsequently up to 30 days post-surgery Pt no bwli srg 30 day srg
G9631 0010 3 Patient sustained ureter injury at the time of surgery or discovered subsequently up to 30 days post-surgery Pt ui srg 30 day pst srg
G9632 0010 3 Documented medical reasons for not reporting ureter injury (e.g., gynecologic or other pelvic malignancy documented, concurrent surgery involving bladder pathology, injury that occurs during a urinary incontinence procedure, patient death from non-medical causes not related to surgery, patient died during procedure without evidence of ureter injury) Med rsn for no rpt uret inj
G9633 0010 3 Patient did not sustain ureter injury at the time of surgery nor discovered subsequently up to 30 days post-surgery Pt no ui srg 30 day pst srg
G9634 0010 3 Health-related quality of life assessed with tool during at least two visits and quality of life score remained the same or improved Qual life tool 2x same/impr
G9635 0010 3 Health-related quality of life not assessed with tool for documented reason(s) (e.g., patient has a cognitive or neuropsychiatric impairment that impairs his/her ability to complete the hrqol survey, patient has the inability to read and/or write in order to complete the hrqol questionnaire) No doc rsn do qual life assm
G9636 0010 3 Health-related quality of life not assessed with tool during at least two visits or quality of life score declined No life asst 2x same/decr
G9637 0010 3 Final reports with documentation of one or more dose reduction techniques (e.g., automated exposure control, adjustment of the ma and/or kv according to patient size, use of iterative reconstruction technique) Doc >1 dose reduc tech
G9638 0010 3 Final reports without documentation of one or more dose reduction techniques (e.g., automated exposure control, adjustment of the ma and/or kv according to patient size, use of iterative reconstruction technique) No doc >1 dose reduc tech
G9639 0010 3 Major amputation or open surgical bypass not required within 48 hours of the index endovascular lower extremity revascularization procedure Amp no reqd in48h ieler proc
G9640 0010 3 Documentation of planned hybrid or staged procedure Doc plan hybrid/stage proc
G9641 0010 3 Major amputation or open surgical bypass required within 48 hours of the index endovascular lower extremity revascularization procedure Amp reqd w/in 48h ieler proc
G9642 0010 3 Current smokers (e.g., cigarette, cigar, pipe, e-cigarette or marijuana) Current smoker
G9643 0010 3 Elective surgery Elective surgery
G9644 0010 3 Patients who abstained from smoking prior to anesthesia on the day of surgery or procedure No smok b/4 anes day of surg
G9645 0010 3 Patients who did not abstain from smoking prior to anesthesia on the day of surgery or procedure Had smoke b/4 anes day surg
G9646 0010 3 Patients with 90 day mrs score of 0 to 2 Pt w/90d mrs 0-2
G9647 0010 3 Patients in whom mrs score could not be obtained at 90 day follow-up No mrs score in 90d followup
G9648 0010 3 Patients with 90 day mrs score greater than 2 Pt w/90d mrs >2
G9649 0010 3 Psoriasis assessment tool documented meeting any one of the specified benchmarks (e.g., (pga; 5-point or 6-point scale), body surface area (bsa), psoriasis area and severity index (pasi) and/or dermatology life quality index) (dlqi)) Psor as doc spc bm
G9650 0010 3 Documentation that the patient declined therapy change or has documented contraindications (e.g., experienced adverse effects or lack of efficacy with all other therapy options) in order to achieve better disease control as measured by pga, bsa, pasi, or dlqi Doc pt no ther chg or contra
G9651 0010 3 Psoriasis assessment tool documented not meeting any one of the specified benchmarks (e.g., (pga; 5-point or 6-point scale), body surface area (bsa), psoriasis area and severity index (pasi) and/or dermatology life quality index) (dlqi)) or psoriasis assessment tool not documented Psor as doc no spc bm
G9652 0010 3 Patient has been treated with a systemic or biologic medication for psoriasis for at least six months Pt tx sys bio med psori 6mth
G9653 0010 3 Patient has not been treated with a systemic or biologic medication for psoriasis for at least six months Pt no tx sys bio rx 6 mths
G9654 0010 3 Monitored anesthesia care (mac) Mon anesth care
G9655 0010 3 A transfer of care protocol or handoff tool/checklist that includes the required key handoff elements is used Toc tool incl key elem
G9656 0010 3 Patient transferred directly from anesthetizing location to pacu or other non-icu location Pt trans from anest to pacu
G9657 0010 3 Transfer of care during an anesthetic or to the intensive care unit Toc dur aneth to icu
G9658 0010 3 A transfer of care protocol or handoff tool/checklist that includes the required key handoff elements is not used Toc tool incl elem not used
G9659 0010 3 Patients greater than 85 years of age who did not have a history of colorectal cancer or valid medical reason for the colonoscopy, including: iron deficiency anemia, lower gastrointestinal bleeding, crohn’s disease (i.e., regional enteritis), familial adenomatous polyposis, lynch syndrome (i.e., hereditary non-polyposis colorectal cancer), inflammatory bowel disease, ulcerative colitis, abnormal finding of gastrointestinal tract, or changes in bowel habits >85y no hx colo ca/rsn scope
G9660 0010 3 Documentation of medical reason(s) for a colonoscopy performed on a patient greater than 85 years of age (e.g., last colonoscopy incomplete, last colonoscopy had inadequate prep, iron deficiency anemia, lower gastrointestinal bleeding, crohn’s disease (i.e., regional enteritis), familial history of adenomatous polyposis, lynch syndrome (i.e., hereditary non-polyposis colorectal cancer), inflammatory bowel disease, ulcerative colitis, abnormal finding of gastrointestinal tract, or changes in bowel habits) Doc med rsn scope pt >85y
G9661 0010 3 Patients greater than 85 years of age who received a routine colonoscopy for a reason other than the following: an assessment of signs/symptoms of gi tract illness, and/or the patient is considered high risk, and/or to follow-up on previously diagnosed advance lesions >85y scope othr rsn
G9662 0010 3 Previously diagnosed or have an active diagnosis of clinical ascvd Prior dx/active clin ascvd
G9663 0010 3 Any fasting or direct ldl-c laboratory test result <= 190 mg/dl Fast/dir ldl <= 190 mg/dl
G9664 0010 3 Patients who are currently statin therapy users or received an order (prescription) for statin therapy Taking statin or rec’d order
G9665 0010 3 Patients who are not currently statin therapy users or did not receive an order (prescription) for statin therapy No statin/no order statin
G9666 0010 3 The highest fasting or direct ldl-c laboratory test result of 70-189 mg/dl in the measurement period or two years prior to the beginning of the measurement period Fas/dir ldl 70-189mg/dl mst
G9667 0010 3 Documentation of medical reason(s) for not currently being a statin therapy user or receive an order (prescription) for statin therapy (e.g., patient with adverse effect, allergy or intolerance to statin medication therapy, patients who have an active diagnosis of pregnancy or who are breastfeeding, patients who are receiving palliative care, patients with active liver disease or hepatic disease or insufficiency, patients with end stage renal disease (esrd), and patients with diabetes who have a fasting or direct ldl-c laboratory test result < 70 mg/dl and are not taking statin therapy) Doc med rsn no stat tx/presc
G9669 0010 3 I intend to report the multiple chronic conditions measures group Intend rpt mult chr msr grp
G9670 0010 3 All quality actions for the applicable measures in the multiple chronic conditions measures group have been performed for this patient Qty act mcc mg perf
G9671 0010 3 I intend to report the diabetic retinopathy measures group Intend rpt dia retin msr grp
G9672 0010 3 All quality actions for the applicable measures in the diabetic retinopathy measures group have been performed for this patient Qty act diab retin mg perf
G9673 0010 3 I intend to report the cardiovascular prevention measures group Intend rpt card prev msr grp
G9674 0010 3 Patients with clinical ascvd diagnosis Pt w/clin ascvd dx
G9675 0010 3 Patients who have ever had a fasting or direct laboratory result of ldl-c = 190 mg/dl Pt w/fast/dir lab ldl-c >190
G9676 0010 3 Patients aged 40 to 75 years at the beginning of the measurement period with type 1 or type 2 diabetes and with an ldl-c result of 70?189 mg/dl recorded as the highest fasting or direct laboratory test result in the measurement year or during the two years prior to the beginning of the measurement period 40-75y w/type 1/2 w/ldl-c rs
G9677 0010 3 All quality actions for the applicable measures in the cardiovascular prevention measures group have been performed for this patient Qty act card prev mg perf
G9678 0010 3 Oncology care model (ocm) monthly enhanced oncology services (meos) payment for ocm enhanced services. g9678 payments may only be made to ocm practitioners for ocm beneficiaries for the furnishment of enhanced services as defined in the ocm participation agreement Oncology care model service
G9679 0010 3 This code is for onsite acute care treatment of a nursing facility resident with pneumonia; may only be billed once per day per beneficiary Acute care pneumonia
G9680 0010 3 This code is for onsite acute care treatment of a nursing facility resident with chf; may only be billed once per day per beneficiary Acute care congestive heart
G9681 0010 3 This code is for onsite acute care treatment of a resident with copd or asthma; may only be billed once per day per beneficiary Acute care chronic obstruct
G9682 0010 3 This code is for the onsite acute care treatment a nursing facility resident with a skin infection; may only be billed once per day per beneficiary Acute care skin infection
G9683 0010 3 Facility service(s) for the onsite acute care treatment of a nursing facility resident with fluid or electrolyte disorder. (may only be billed once per day per beneficiary). this service is for a demonstration project Acute fluid/electro disorder
G9684 0010 3 This code is for the onsite acute care treatment of a nursing facility resident for a uti; may only be billed once per day per beneficiary Acute care urinary tract inf
G9685 0010 3 Physician service or other qualified health care professional for the evaluation and management of a beneficiary’s acute change in condition in a nursing facility. this service is for a demonstration project Acute nursing facility care
G9686 0010 3 Onsite nursing facility conference, that is separate and distinct from an evaluation and management visit, including qualified practitioner and at least one member of the nursing facility interdisciplinary care team Nursing facility conference
G9687 0010 3 Hospice services provided to patient any time during the measurement period Hospice anytime msmt per
G9688 0010 3 Patients using hospice services any time during the measurement period Pt w/hosp anytime msmt per
G9689 0010 3 Patient admitted for performance of elective carotid intervention Inpt elect carotid intervent
G9690 0010 3 Patient receiving hospice services any time during the measurement period Pt in hos
G9691 0010 3 Patient had hospice services any time during the measurement period Pt hosp dur msmt period
G9692 0010 3 Hospice services received by patient any time during the measurement period Hosp recd by pt dur msmt per
G9693 0010 3 Patient use of hospice services any time during the measurement period Pt use hosp during msmt per
G9694 0010 3 Hospice services utilized by patient any time during the measurement period Hosp srv used pt in msmt per
G9695 0010 3 Long-acting inhaled bronchodilator prescribed Long act inhal bronchdil pre
G9696 0010 3 Documentation of medical reason(s) for not prescribing a long-acting inhaled bronchodilator Med rsn no presc bronchdil
G9697 0010 3 Documentation of patient reason(s) for not prescribing a long-acting inhaled bronchodilator Pt rsn no presc bronchdil
G9698 0010 3 Documentation of system reason(s) for not prescribing a long-acting inhaled bronchodilator Sys rsn no presc bronchdil
G9699 0010 3 Long-acting inhaled bronchodilator not prescribed, reason not otherwise specified Long inhal bronchdil no pres
G9700 0010 3 Patients who use hospice services any time during the measurement period Pt is w/hosp during msmt per
G9701 0010 3 Children who are taking antibiotics in the 30 days prior to the date of the encounter during which the diagnosis was established Child anbx 30 prior dx estab
G9702 0010 3 Patients who use hospice services any time during the measurement period Pt use hosp during msmt per
G9703 0010 3 Children who are taking antibiotics in the 30 days prior to the diagnosis of pharyngitis Child anbx 30 prior dx phary
G9704 0010 3 Ajcc breast cancer stage i: t1 mic or t1a documented Ajcc br ca stg i: t1 mic/t1a
G9705 0010 3 Ajcc breast cancer stage i: t1b (tumor > 0.5 cm but <= 1 cm in greatest dimension) documented Ajcc br ca stg ib
G9706 0010 3 Low (or very low) risk of recurrence, prostate cancer Low recur prost ca
G9707 0010 3 Patient received hospice services any time during the measurement period Pt had hosp dur msmt per
G9708 0010 3 Women who had a bilateral mastectomy or who have a history of a bilateral mastectomy or for whom there is evidence of a right and a left unilateral mastectomy Bilat mast/hx bi /unilat mas
G9709 0010 3 Hospice services used by patient any time during the measurement period Hosp srv used pt in msmt per
G9710 0010 3 Patient was provided hospice services any time during the measurement period Pt prov hosp srv msmt per
G9711 0010 3 Patients with a diagnosis or past history of total colectomy or colorectal cancer Pt hx tot col or colon ca
G9712 0010 3 Documentation of medical reason(s) for prescribing or dispensing antibiotic (e.g., intestinal infection, pertussis, bacterial infection, lyme disease, otitis media, acute sinusitis, acute pharyngitis, acute tonsillitis, chronic sinusitis, infection of the pharynx/larynx/tonsils/adenoids, prostatitis, cellulitis/ mastoiditis/bone infections, acute lymphadenitis, impetigo, skin staph infections, pneumonia, gonococcal infections/venereal disease (syphilis, chlamydia, inflammatory diseases [female reproductive organs]), infections of the kidney, cystitis/uti, acne, hiv disease/asymptomatic hiv, cystic fibrosis, disorders of the immune system, malignancy neoplasms, chronic bronchitis, emphysema, bronchiectasis, extrinsic allergic alveolitis, chronic airway obstruction, chronic obstructive asthma, pneumoconiosis and other lung disease due to external agents, other diseases of the respiratory system, and tuberculosis Doc med rsn presc anbx
G9713 0010 3 Patients who use hospice services any time during the measurement period Pt use hosp during msmt per
G9714 0010 3 Patient is using hospice services any time during the measurement period Pt is w/hosp during msmt per
G9715 0010 3 Patients who use hospice services any time during the measurement period Pt w/hosp anytime msmt per
G9716 0010 3 Bmi is documented as being outside of normal limits, follow-up plan is not completed for documented reason Bmi doc onl fup not cmpltd
G9717 0010 3 Documentation stating the patient has an active diagnosis of depression or has a diagnosed bipolar disorder, therefore screening or follow-up not required Doc pt dx dep/bp f/u nt req
G9718 0010 3 Hospice services for patient provided any time during the measurement period Hospice anytime msmt per
G9719 0010 3 Patient is not ambulatory, bed ridden, immobile, confined to chair, wheelchair bound, dependent on helper pushing wheelchair, independent in wheelchair or minimal help in wheelchair Pt not ambul/immob/wc
G9720 0010 3 Hospice services for patient occurred any time during the measurement period Hospice anytime msmt per
G9721 0010 3 Patient not ambulatory, bed ridden, immobile, confined to chair, wheelchair bound, dependent on helper pushing wheelchair, independent in wheelchair or minimal help in wheelchair Pt not ambul/immob/wc
G9722 0010 3 Documented history of renal failure or baseline serum creatinine = 4.0 mg/dl; renal transplant recipients are not considered to have preoperative renal failure, unless, since transplantation the cr has been or is 4.0 or higher Doc hx renal fail or cr+ >4
G9723 0010 3 Hospice services for patient received any time during the measurement period Hosp recd by pt dur msmt per
G9724 0010 3 Patients who had documentation of use of anticoagulant medications overlapping the measurement year Pt w/doc use anticoag mst yr
G9725 0010 3 Patients who use hospice services any time during the measurement period Pt w/hosp anytime msmt per
G9726 0010 3 Patient refused to participate Refused to participate
G9727 0010 3 Patient unable to complete the knee fs prom at initial evaluation and/or discharge due to blindness, illiteracy, severe mental incapacity or language incompatibility and an adequate proxy is not available Pt unable cmplt knee fs prom
G9728 0010 3 Patient refused to participate Refused to participate
G9729 0010 3 Patient unable to complete the hip fs prom at initial evaluation and discharge due to blindness, illiteracy, severe mental incapacity or language incompatibility and an adequate proxy is not available Pt unbl cmplt hip fs prom
G9730 0010 3 Patient refused to participate Refused to participate
G9731 0010 3 Patient unable to complete the ankle/foot fs prom at initial evaluation and/or discharge due to blindness, illiteracy, severe mental incapacity or language incompatibility and an adequate proxy is not available Pt unbl cmplt ft/ank fs prom
G9732 0010 3 Patient refused to participate Refused to participate
G9733 0010 3 Patient unable to complete the low back fs prom at initial evaluation and/or discharge due to blindness, illiteracy, severe mental incapacity or language incompatibility and an adequate proxy is not available Pt unbl cmplt lb fs prom
G9734 0010 3 Patient refused to participate Refused to participate
G9735 0010 3 Patient unable to complete the shoulder fs prom at initial evaluation and/or discharge due to blindness, illiteracy, severe mental incapacity or language incompatibility and an adequate proxy is not available Pt unbl cmplt shld fs prom
G9736 0010 3 Patient refused to participate Refused to participate
G9737 0010 3 Patient unable to complete the elbow/wrist/hand fs prom at initial evaluation and/or discharge due to blindness, illiteracy, severe mental incapacity or language incompatibility and an adequate proxy is not available Pt unbl cmplt ewh fs prom
G9738 0010 3 Patient refused to participate Refused to participate
G9739 0010 3 Patient unable to complete the general orthopedic fs prom at initial evaluation and/or discharge due to blindness, illiteracy, severe mental incapacity or language incompatibility and an adequate proxy is not available Pt unbl cmplt go fs prom
G9740 0010 3 Hospice services given to patient any time during the measurement period Hosp srv to pt dur msmt per
G9741 0010 3 Patients who use hospice services any time during the measurement period Pt w/hosp anytime msmt per
G9742 0010 3 Psychiatric symptoms assessed Psych sympt assessed
G9743 0010 3 Psychiatric symptoms not assessed, reason not otherwise specified Psych symp not assessed, rns
G9744 0010 3 Patient not eligible due to active diagnosis of hypertension Pt not eli d/t act dig htn
G9745 0010 3 Documented reason for not screening or recommending a follow-up for high blood pressure Doc rsn no hbp scrn or f/u
G9746 0010 3 Patient has mitral stenosis or prosthetic heart valves or patient has transient or reversible cause of af (e.g., pneumonia, hyperthyroidism, pregnancy, cardiac surgery) Mit sten, valve or trans af
G9747 0010 3 Patient is undergoing palliative dialysis with a catheter Pall dialysis with catheter
G9748 0010 3 Patient approved by a qualified transplant program and scheduled to receive a living donor kidney transplant App transpl lvg kidney donor
G9749 0010 3 Patient is undergoing palliative dialysis with a catheter Pall dialysis with catheter
G9750 0010 3 Patient approved by a qualified transplant program and scheduled to receive a living donor kidney transplant App transpl lvg kidney donor
G9751 0010 3 Patient died at any time during the 24-month measurement period Pt died w/in 24 mos rpt time
G9752 0010 3 Emergency surgery Urgent surgery
G9753 0010 3 Documentation of medical reason for not conducting a search for dicom format images for prior patient ct imaging studies completed at non-affiliated external healthcare facilities or entities within the past 12 months that are available through a secure, authorized, media-free, shared archive (e.g., trauma, acute myocardial infarction, stroke, aortic aneurysm where time is of the essence) Doc no dicom, ct other fac
G9754 0010 3 A finding of an incidental pulmonary nodule Incid pulm nodule
G9755 0010 3 Documentation of medical reason(s) for not including a recommended interval and modality for follow-up or for no follow-up, and source of recommendations (e.g., patients with unexplained fever, immunocompromised patients who are at risk for infection) Doc med rsn no fllw up
G9756 0010 3 Surgical procedures that included the use of silicone oil Surg proc w/silicone oil
G9757 0010 3 Surgical procedures that included the use of silicone oil Surg proc w/silicone oil
G9758 0010 3 Patient in hospice at any time during the measurement period Pt in hos
G9759 0010 3 History of preoperative posterior capsule rupture Hx preop post cap rup
G9760 0010 3 Patients who use hospice services any time during the measurement period Pt w/hosp anytime msmt per
G9761 0010 3 Patients who use hospice services any time during the measurement period Pt w/hosp anytime msmt per
G9762 0010 3 Patient had at least two hpv vaccines (with at least 146 days between the two) or three hpv vaccines on or between the patient’s 9th and 13th birthdays Pt had >= 2-3 hpv vaccines
G9763 0010 3 Patient did not have at least two hpv vaccines (with at least 146 days between the two) or three hpv vaccines on or between the patient’s 9th and 13th birthdays Pt not have 2-3 hpv vaccines
G9764 0010 3 Patient has been treated with a systemic medication for psoriasis vulgaris Pt treatd w/oral syst or bio
G9765 0010 3 Documentation that the patient declined change in medication or alternative therapies were unavailable, has documented contraindications, or has not been treated with a systemic medication for at least six consecutive months (e.g., experienced adverse effects or lack of efficacy with all other therapy options) in order to achieve better disease control as measured by pga, bsa, pasi, or dlqi Doc pat declined therapy
G9766 0010 3 Patients who are transferred from one institution to another with a known diagnosis of cva for endovascular stroke treatment Cva stroke dx tx transf fac
G9767 0010 3 Hospitalized patients with newly diagnosed cva considered for endovascular stroke treatment Hosp new dx cva consid evst
G9768 0010 3 Patients who utilize hospice services any time during the measurement period Pt w/hosp anytime msmt per
G9769 0010 3 Patient had a bone mineral density test in the past two years or received osteoporosis medication or therapy in the past 12 months Bn den 2yr/got ost med/ther
G9770 0010 3 Peripheral nerve block (pnb) Perip nerve block
G9771 0010 3 At least 1 body temperature measurement equal to or greater than 35.5 degrees celsius (or 95.9 degrees fahrenheit) achieved within the 30 minutes immediately before or the 15 minutes immediately after anesthesia end time Anes end, 1 temp >35.5(95.9)
G9772 0010 3 Documentation of medical reason(s) for not achieving at least 1 body temperature measurement equal to or greater than 35.5 degrees celsius (or 95.9 degrees fahrenheit) within the 30 minutes immediately before or the 15 minutes immediately after anesthesia end time (e.g., emergency cases, intentional hypothermia, etc.) Doc med rsn no temp >= 35.5
G9773 0010 3 At least 1 body temperature measurement equal to or greater than 35.5 degrees celsius (or 95.9 degrees fahrenheit) not achieved within the 30 minutes immediately before or the 15 minutes immediately after anesthesia end time, reason not given 1 bod temp >=35.5
G9774 0010 3 Patients who have had a hysterectomy Pt had hyst
G9775 0010 3 Patient received at least 2 prophylactic pharmacologic anti-emetic agents of different classes preoperatively and/or intraoperatively Recd 2 anti-emet pre/intraop
G9776 0010 3 Documentation of medical reason for not receiving at least 2 prophylactic pharmacologic anti-emetic agents of different classes preoperatively and/or intraoperatively (e.g., intolerance or other medical reason) Doc med rsn no proph antiem
G9777 0010 3 Patient did not receive at least 2 prophylactic pharmacologic anti-emetic agents of different classes preoperatively and/or intraoperatively Pt no antiemet pre/intraop
G9778 0010 3 Patients who have a diagnosis of pregnancy Pts dx w/pregn
G9779 0010 3 Patients who are breastfeeding Pts breastfeeding
G9780 0010 3 Patients who have a diagnosis of rhabdomyolysis Pts dx w/rhabdomyolysis
G9781 0010 3 Documentation of medical reason(s) for not currently being a statin therapy user or receive an order (prescription) for statin therapy (e.g., patient with adverse effect, allergy or intolerance to statin medication therapy, patients who are receiving palliative or hospice care, patients with active liver disease or hepatic disease or insufficiency, and patients with end stage renal disease (esrd)) Doc rsn no statin
G9782 0010 3 History of or active diagnosis of familial or pure hypercholesterolemia Hx dx fam/pure hypercholes
G9783 0010 3 Documentation of patients with diabetes who have a most recent fasting or direct ldl- c laboratory test result < 70 mg/dl and are not taking statin therapy Doc dx dm, fast <70, no stat
G9784 0010 3 Pathologists/dermatopathologists providing a second opinion on a biopsy Path/derm prov 2nd biop opin
G9785 0010 3 Pathology report diagnosing cutaneous basal cell carcinoma, squamous cell carcinoma, or melanoma (to include in situ disease) sent from the pathologist/ dermatopathologist to the biopsying clinician for review within 7 days from the time when the tissue specimen was received by the pathologist Path report sent
G9786 0010 3 Pathology report diagnosing cutaneous basal cell carcinoma, squamous cell carcinoma, or melanoma (to include in situ disease) was not sent from the pathologist/ dermatopathologist to the biopsying clinician for review within 7 days from the time when the tissue specimen was received by the pathologist Path report not sent
G9787 0010 3 Patient alive as of the last day of the measurement year Pt alive
G9788 0010 3 Most recent bp is less than or equal to 140/90 mm hg Most rct bp </= 140/90
G9789 0010 3 Blood pressure recorded during inpatient stays, emergency room visits, urgent care visits, and patient self-reported bp’s (home and health fair bp results) Record bp ip, er, urg/self
G9790 0010 3 Most recent bp is greater than 140/90 mm hg, or blood pressure not documented Most rct bp >/= 140/90
G9791 0010 3 Most recent tobacco status is tobacco free Most rct tob stat free
G9792 0010 3 Most recent tobacco status is not tobacco free Most rct tob stat not free
G9793 0010 3 Patient is currently on a daily aspirin or other antiplatelet Pt on daily asa/antiplat
G9794 0010 3 Documentation of medical reason(s) for not on a daily aspirin or other antiplatelet (e.g., history of gastrointestinal bleed, intra-cranial bleed, idiopathic thrombocytopenic purpura (itp), gastric bypass or documentation of active anticoagulant use during the measurement period) Doc med rsn no daily aspirin
G9795 0010 3 Patient is not currently on a daily aspirin or other antiplatelet Pt no daily asa/antiplat
G9796 0010 3 Patient is currently on a statin therapy Pt not currently on statin
G9797 0010 3 Patient is not on a statin therapy Pt currently on statin
G9798 0010 3 Discharge(s) for ami between july 1 of the year prior measurement period to june 30 of the measurement period D/c ami btw 7/1-6/30 meas pd
G9799 0010 3 Patients with a medication dispensing event indicator of a history of asthma any time during the patient’s history through the end of the measure period Med disp evt indic hx asth
G9800 0010 3 Patients who are identified as having an intolerance or allergy to beta-blocker therapy Pt id intol/alleg beta-block
G9801 0010 3 Hospitalizations in which the patient was transferred directly to a non-acute care facility for any diagnosis Nonacut transf from inpt
G9802 0010 3 Patients who use hospice services any time during the measurement period Pt w/hosp anytime msmt per
G9803 0010 3 Patient prescribed at least a 135 day treatment within the 180-day measurement interval with beta-blockers post-discharge for ami Pt presc 135 day trmt
G9804 0010 3 Patient was not prescribed at least a 135 day treatment within the 180-day measurement interval with beta-blockers post-discharge for ami Pt not presc 135 day trmt
G9805 0010 3 Patients who use hospice services any time during the measurement period Pt w/hosp anytime msmt per
G9806 0010 3 Patients who received cervical cytology or an hpv test Pt recd cerv cyto/hpv
G9807 0010 3 Patients who did not receive cervical cytology or an hpv test Pt no recd cerv cyto/hpv
G9808 0010 3 Any patients who had no asthma controller medications dispensed during the measurement year Pt no asthm cont med mst per
G9809 0010 3 Patients who use hospice services any time during the measurement period Pt w/hosp anytime msmt per
G9810 0010 3 Patient achieved a pdc of at least 75% for their asthma controller medication Pdc 75% w/asth cont med
G9811 0010 3 Patient did not achieve a pdc of at least 75% for their asthma controller medication No pdc 75% w/asth cont med
G9812 0010 3 Patient died including all deaths occurring during the hospitalization in which the operation was performed, even if after 30 days, and those deaths occurring after discharge from the hospital, but within 30 days of the procedure Pt died during inpt/30d aft
G9813 0010 3 Patient did not die within 30 days of the procedure or during the index hospitalization Pt not died w/in 30d of proc
G9814 0010 3 Death occurring during the index acute care hospitalization Death during index hosp
G9815 0010 3 Death did not occur during the index acute care hospitalization Death not during index hosp
G9816 0010 3 Death occurring after discharge from the hospital but within 30 days post procedure Death <30 day post discharge
G9817 0010 3 Death did not occur after discharge from the hospital within 30 days post procedure No death 30-days post-disch
G9818 0010 3 Documentation of sexual activity Doc sex activity
G9819 0010 3 Patients who use hospice services any time during the measurement period Pt w/hosp anytime msmt per
G9820 0010 3 Documentation of a chlamydia screening test with proper follow-up Doc chlam scr test w/follow
G9821 0010 3 No documentation of a chlamydia screening test with proper follow-up No doc chlam scr ts w/follow
G9822 0010 3 Women who had an endometrial ablation procedure during the year prior to the index date (exclusive of the index date) Endo abl proc yr prev ind dt
G9823 0010 3 Endometrial sampling or hysteroscopy with biopsy and results documented Endo smpl/hyst bx res doc
G9824 0010 3 Endometrial sampling or hysteroscopy with biopsy and results not documented Endo smpl/hyst bx res no doc
G9825 0010 3 Her-2/neu negative or undocumented/unknown Her-2 neg,undoc/unkn
G9826 0010 3 Patient transferred to practice after initiation of chemotherapy Transf pract aft init chemo
G9827 0010 3 Her2-targeted therapies not administered during the initial course of treatment Her-2 targ ther no init tx
G9828 0010 3 Her2-targeted therapies administered during the initial course of treatment Her-2 targ ther dur init tx
G9829 0010 3 Breast adjuvant chemotherapy administered Breast adj chemo admin
G9830 0010 3 Her-2/neu positive Her-2 pos
G9831 0010 3 Ajcc stage at breast cancer diagnosis = ii or iii Ajcc stg brt ca dx ii or iii
G9832 0010 3 Ajcc stage at breast cancer diagnosis = i (ia or ib) and t-stage at breast cancer diagnosis does not equal = t1, t1a, t1b Brt ca dx i, no t1/t1a/t1b
G9833 0010 3 Patient transfer to practice after initiation of chemotherapy Transf pract aft init chemo
G9834 0010 3 Patient has metastatic disease at diagnosis Pt met dis at dx
G9835 0010 3 Trastuzumab administered within 12 months of diagnosis Trastuz given w/in 12 mos dx
G9836 0010 3 Reason for not administering trastuzumab documented (e.g. patient declined, patient died, patient transferred, contraindication or other clinical exclusion, neoadjuvant chemotherapy or radiation not complete) Rsn no trast given doc
G9837 0010 3 Trastuzumab not administered within 12 months of diagnosis Trastuz not in 12 mos dx
G9838 0010 3 Patient has metastatic disease at diagnosis Pt met dis at dx
G9839 0010 3 Anti-egfr monoclonal antibody therapy Anti-egfr mon anti ther
G9840 0010 3 Ras (kras and nras) gene mutation testing performed before initiation of anti-egfr moab Gene testing performed
G9841 0010 3 Ras (kras and nras) gene mutation testing not performed before initiation of anti-egfr moab Gene testing not performed
G9842 0010 3 Patient has metastatic disease at diagnosis Pt met dis at dx
G9843 0010 3 Ras (kras or nras) gene mutation Kras or nras gene mutation
G9844 0010 3 Patient did not receive anti-egfr monoclonal antibody therapy Pt no recd anti-egfr ther
G9845 0010 3 Patient received anti-egfr monoclonal antibody therapy Pt recd anti-egfr ther
G9846 0010 3 Patients who died from cancer Pt died from cancer
G9847 0010 3 Patient received chemotherapy in the last 14 days of life Pt recd chemo last 14d life
G9848 0010 3 Patient did not receive chemotherapy in the last 14 days of life Pt no chemo last 14d life
G9849 0010 3 Patients who died from cancer Pt died from cancer
G9850 0010 3 Patient had more than one emergency department visit in the last 30 days of life 1/more ed last 30d life
G9851 0010 3 Patient had one or less emergency department visits in the last 30 days of life 1/no ed visit last 30d life
G9852 0010 3 Patients who died from cancer Pt died from cancer
G9853 0010 3 Patient admitted to the icu in the last 30 days of life Icu stay last 30d life
G9854 0010 3 Patient was not admitted to the icu in the last 30 days of life No icu stay last 30d life
G9855 0010 3 Patients who died from cancer Pt died from cancer
G9856 0010 3 Patient was not admitted to hospice Pt no hospice
G9857 0010 3 Patient admitted to hospice Pt admit hospice
G9858 0010 3 Patient enrolled in hospice Pt enroll hospice
G9859 0010 3 Patients who died from cancer Pt died from cancer
G9860 0010 3 Patient spent less than three days in hospice care Pt less 3d hospice
G9861 0010 3 Patient spent greater than or equal to three days in hospice care Pt more than 3d hospice
G9862 0010 3 Documentation of medical reason(s) for not recommending at least a 10 year follow-up interval (e.g., inadequate prep, familial or personal history of colonic polyps, patient had no adenoma and age is = 66 years old, or life expectancy < 10 years old, other medical reasons) Doc rsn no 10 yr follow
G9868 0010 3 Receipt and analysis of remote, asynchronous images for dermatologic and/or ophthalmologic evaluation, for use under the next generation aco model, less than 10 minutes Next gen aco model <10min
G9869 0010 3 Receipt and analysis of remote, asynchronous images for dermatologic and/or ophthalmologic evaluation, for use under the next generation aco model, 10-20 minutes Next gen aco model 10-20min
G9870 0010 3 Receipt and analysis of remote, asynchronous images for dermatologic and/or ophthalmologic evaluation, for use under the next generation aco model, 20 or more minutes Next gen aco model >20min
G9873 0010 3 First medicare diabetes prevention program (mdpp) core session was attended by an mdpp beneficiary under the mdpp expanded model (em). a core session is an mdpp service that: (1) is furnished by an mdpp supplier during months 1 through 6 of the mdpp services period; (2) is approximately 1 hour in length; and (3) adheres to a cdc-approved dpp curriculum for core sessions 1 em core session
G9874 0010 3 Four total medicare diabetes prevention program (mdpp) core sessions were attended by an mdpp beneficiary under the mdpp expanded model (em). a core session is an mdpp service that: (1) is furnished by an mdpp supplier during months 1 through 6 of the mdpp services period; (2) is approximately 1 hour in length; and (3) adheres to a cdc-approved dpp curriculum for core sessions 4 em core sessions
G9875 0010 3 Nine total medicare diabetes prevention program (mdpp) core sessions were attended by an mdpp beneficiary under the mdpp expanded model (em). a core session is an mdpp service that: (1) is furnished by an mdpp supplier during months 1 through 6 of the mdpp services period; (2) is approximately 1 hour in length; and (3) adheres to a cdc-approved dpp curriculum for core sessions 9 em core sessions
G9876 0010 3 Two medicare diabetes prevention program (mdpp) core maintenance sessions (ms) were attended by an mdpp beneficiary in months (mo) 7-9 under the mdpp expanded model (em). a core maintenance session is an mdpp service that: (1) is furnished by an mdpp supplier during months 7 through 12 of the mdpp services period; (2) is approximately 1 hour in length; and (3) adheres to a cdc-approved dpp curriculum for maintenance sessions. the beneficiary did not achieve at least 5% weight loss (wl) from his/her baseline weight, as measured by at least one in-person weight measurement at a core maintenance session in months 7-9 2 em core ms mo 7-9 no wl
G9877 0010 3 Two medicare diabetes prevention program (mdpp) core maintenance sessions (ms) were attended by an mdpp beneficiary in months (mo) 10-12 under the mdpp expanded model (em). a core maintenance session is an mdpp service that: (1) is furnished by an mdpp supplier during months 7 through 12 of the mdpp services period; (2) is approximately 1 hour in length; and (3) adheres to a cdc-approved dpp curriculum for maintenance sessions. the beneficiary did not achieve at least 5% weight loss (wl) from his/her baseline weight, as measured by at least one in-person weight measurement at a core maintenance session in months 10-12 2 em core ms mo 10-12 no wl
G9878 0010 3 Two medicare diabetes prevention program (mdpp) core maintenance sessions (ms) were attended by an mdpp beneficiary in months (mo) 7-9 under the mdpp expanded model (em). a core maintenance session is an mdpp service that: (1) is furnished by an mdpp supplier during months 7 through 12 of the mdpp services period; (2) is approximately 1 hour in length; and (3) adheres to a cdc-approved dpp curriculum for maintenance sessions.the beneficiary achieved at least 5% weight loss (wl) from his/her baseline weight, as measured by at least one in-person weight measurement at a core maintenance session in months 7-9 2 em core ms mo 7-9 wl
G9879 0010 3 Two medicare diabetes prevention program (mdpp) core maintenance sessions (ms) were attended by an mdpp beneficiary in months (mo) 10-12 under the mdpp expanded model (em). a core maintenance session is an mdpp service that: (1) is furnished by an mdpp supplier during months 7 through 12 of the mdpp services period; (2) is approximately 1 hour in length; and (3) adheres to a cdc-approved dpp curriculum for maintenance sessions. the beneficiary achieved at least 5% weight loss (wl) from his/her baseline weight, as measured by at least one in-person weight measurement at a core maintenance session in months 10-12 2 em core ms mo 10-12 wl
G9880 0010 3 The mdpp beneficiary achieved at least 5% weight loss (wl) from his/her baseline weight in months 1-12 of the mdpp services period under the mdpp expanded model (em). this is a one-time payment available when a beneficiary first achieves at least 5% weight loss from baseline as measured by an in-person weight measurement at a core session or core maintenance session Em 5 percent wl
G9881 0010 3 The mdpp beneficiary achieved at least 9% weight loss (wl) from his/her baseline weight in months 1-24 under the mdpp expanded model (em). this is a one-time payment available when a beneficiary first achieves at least 9% weight loss from baseline as measured by an in-person weight measurement at a core session, core maintenance session, or ongoing maintenance session Em 9 percent wl
G9882 0010 3 Two medicare diabetes prevention program (mdpp) ongoing maintenance sessions (ms) were attended by an mdpp beneficiary in months (mo) 13-15 under the mdpp expanded model (em). an ongoing maintenance session is an mdpp service that: (1) is furnished by an mdpp supplier during months 13 through 24 of the mdpp services period; (2) is approximately 1 hour in length; and (3) adheres to a cdc-approved dpp curriculum for maintenance sessions. the beneficiary maintained at least 5% weight loss (wl) from his/her baseline weight, as measured by at least one in-person weight measurement at an ongoing maintenance session in months 13-15 2 em ongoing ms mo 13-15 wl
G9883 0010 3 Two medicare diabetes prevention program (mdpp) ongoing maintenance sessions (ms) were attended by an mdpp beneficiary in months (mo) 16-18 under the mdpp expanded model (em). an ongoing maintenance session is an mdpp service that: (1) is furnished by an mdpp supplier during months 13 through 24 of the mdpp services period; (2) is approximately 1 hour in length; and (3) adheres to a cdc-approved dpp curriculum for maintenance sessions. the beneficiary maintained at least 5% weight loss (wl) from his/her baseline weight, as measured by at least one in-person weight measurement at an ongoing maintenance session in months 16-18 2 em ongoing ms mo 16-18 wl
G9884 0010 3 Two medicare diabetes prevention program (mdpp) ongoing maintenance sessions (ms) were attended by an mdpp beneficiary in months (mo) 19-21 under the mdpp expanded model (em). an ongoing maintenance session is an mdpp service that: (1) is furnished by an mdpp supplier during months 13 through 24 of the mdpp services period; (2) is approximately 1 hour in length; and (3) adheres to a cdc-approved dpp curriculum for maintenance sessions. the beneficiary maintained at least 5% weight loss (wl) from his/her baseline weight, as measured by at least one in-person weight measurement at an ongoing maintenance session in months 19-21 2 em ongoing ms mo 19-21 wl
G9885 0010 3 Two medicare diabetes prevention program (mdpp) ongoing maintenance sessions (ms) were attended by an mdpp beneficiary in months (mo) 22-24 under the mdpp expanded model (em). an ongoing maintenance session is an mdpp service that: (1) is furnished by an mdpp supplier during months 13 through 24 of the mdpp services period; (2) is approximately 1 hour in length; and (3) adheres to a cdc-approved dpp curriculum for maintenance sessions. the beneficiary maintained at least 5% weight loss (wl) from his/her baseline weight, as measured by at least one in-person weight measurement at an ongoing maintenance session in months 22-24 2 em ongoing ms mo 22-24 wl
G9890 0010 3 Bridge payment: a one-time payment for the first medicare diabetes prevention program (mdpp) core session, core maintenance session, or ongoing maintenance session furnished by an mdpp supplier to an mdpp beneficiary during months 1-24 of the mdpp expanded model (em) who has previously received mdpp services from a different mdpp supplier under the mdpp expanded model. a supplier may only receive one bridge payment per mdpp beneficiary Em bridge payment
G9891 0010 3 Mdpp session reported as a line-item on a claim for a payable mdpp expanded model (em) hcpcs code for a session furnished by the billing supplier under the mdpp expanded model and counting toward achievement of the attendance performance goal for the payable mdpp expanded model hcpcs code (this code is for reporting purposes only) Em session reporting
G9892 0010 3 Documentation of patient reason(s) for not performing a dilated macular examination Doc pt rsn no dil mac exam
G9893 0010 3 Dilated macular exam was not performed, reason not otherwise specified No mac exam
G9894 0010 3 Androgen deprivation therapy prescribed/administered in combination with external beam radiotherapy to the prostate Adr dep thrpy prescribed
G9895 0010 3 Documentation of medical reason(s) for not prescribing/administering androgen deprivation therapy in combination with external beam radiotherapy to the prostate (e.g., salvage therapy) Doc med rsn no adr dep thrpy
G9896 0010 3 Documentation of patient reason(s) for not prescribing/administering androgen deprivation therapy in combination with external beam radiotherapy to the prostate Doc pt rsn no adr dep thrpy
G9897 0010 3 Patients who were not prescribed/administered androgen deprivation therapy in combination with external beam radiotherapy to the prostate, reason not given Pt nt prsc adr dep thrpy rng
G9898 0010 3 Patient age 65 or older in institutional special needs plans (snp) or residing in long-term care with pos code 32, 33, 34, 54, or 56 for more than 90 days during the measurement period Pt 66+ snp or ltc pos
G9899 0010 3 Screening, diagnostic, film, digital or digital breast tomosynthesis (3d) mammography results documented and reviewed Scrn mam perf rslts doc
G9900 0010 3 Screening, diagnostic, film, digital or digital breast tomosynthesis (3d) mammography results were not documented and reviewed, reason not otherwise specified Scrn mam perf rslts not doc
G9901 0010 3 Patient age 65 or older in institutional special needs plans (snp) or residing in long-term care with pos code 32, 33, 34, 54, or 56 for more than 90 days during the measurement period Pt 66+ snp or ltc pos
G9902 0010 3 Patient screened for tobacco use and identified as a tobacco user Pt scrn tbco and id as user
G9903 0010 3 Patient screened for tobacco use and identified as a tobacco non-user Pt scrn tbco id as non user
G9904 0010 3 Documentation of medical reason(s) for not screening for tobacco use (e.g., limited life expectancy, other medical reason) Doc med rsn no tbco scrn
G9905 0010 3 Patient not screened for tobacco use, reason not given No pt tbco scrn rng
G9906 0010 3 Patient identified as a tobacco user received tobacco cessation intervention (counseling and/or pharmacotherapy) Pt recv tbco cess interv
G9907 0010 3 Documentation of medical reason(s) for not providing tobacco cessation intervention (e.g., limited life expectancy, other medical reason) Doc med rsn no tbco interv
G9908 0010 3 Patient identified as tobacco user did not receive tobacco cessation intervention (counseling and/or pharmacotherapy), reason not given No pt tbco cess interv rng
G9909 0010 3 Documentation of medical reason(s) for not providing tobacco cessation intervention if identified as a tobacco user (eg, limited life expectancy, other medical reason) Doc med rsn no tbco interv
G9910 0010 3 Patients age 66 or older in institutional special needs plans (snp) or residing in long-term care with pos code 32, 33, 34, 54 or 56 for more than 90 days during the measurement period Pt 66+ snp or ltc pos
G9911 0010 3 Clinically node negative (t1n0m0 or t2n0m0) invasive breast cancer before or after neoadjuvant systemic therapy Node neg pre/post syst ther
G9912 0010 3 Hepatitis b virus (hbv) status assessed and results interpreted prior to initiating anti-tnf (tumor necrosis factor) therapy Hbv status assesed and int
G9913 0010 3 Hepatitis b virus (hbv) status not assessed and results interpreted prior to initiating anti-tnf (tumor necrosis factor) therapy, reason not given No hbv status assesd and int
G9914 0010 3 Patient receiving an anti-tnf agent Pt receiving anti-tnf agent
G9915 0010 3 No record of hbv results documented No documntd hbv results rcd
G9916 0010 3 Functional status performed once in the last 12 months Funct status past 12 months
G9917 0010 3 Documentation of advanced stage dementia and caregiver knowledge is limited Adv dem crgvr limited
G9918 0010 3 Functional status not performed, reason not otherwise specified No funct stat perf, rsn nos
G9919 0010 3 Screening performed and positive and provision of recommendations Scrn nd pos nd prov of rec
G9920 0010 3 Screening performed and negative Scrning perf and negative
G9921 0010 3 No screening performed, partial screening performed or positive screen without recommendations and reason is not given or otherwise specified No or part scrn nd rng or os
G9922 0010 3 Safety concerns screen provided and if positive then documented mitigation recommendations Sfty cncrns scrn nd mit recs
G9923 0010 3 Safety concerns screen provided and negative Safty cncrns scrn and neg
G9924 0010 3 Documentation of medical reason(s) for not providing safety concerns screen or for not providing recommendations, orders or referrals for positive screen (e.g., patient in palliative care, other medical reason) Doc med rsn no scrn or recs
G9925 0010 3 Safety concerns screening not provided, reason not otherwise specified No scrn prov rsn nos
G9926 0010 3 Safety concerns screening positive screen is without provision of mitigation recommendations, including but not limited to referral to other resources Sfty cncrns scrn but no recs
G9927 0010 3 Documentation of system reason(s) for not prescribing warfarin or another fda-approved anticoagulation due to patient being currently enrolled in a clinical trial related to af/atrial flutter treatment Doc no warf /fda pt trial
G9928 0010 3 Warfarin or another fda-approved anticoagulant not prescribed, reason not given No warf or fda drug presc
G9929 0010 3 Patient with transient or reversible cause of af (e.g., pneumonia, hyperthyroidism, pregnancy, cardiac surgery) Trs/rev af
G9930 0010 3 Patients who are receiving comfort care only Com care
G9931 0010 3 Documentation of cha2ds2-vasc risk score of 0 or 1 No chad or chad scr 0 or 1
G9932 0010 3 Documentation of patient reason(s) for not having records of negative or managed positive tb screen (e.g., patient does not return for mantoux (ppd) skin test evaluation) Doc pt rsn no tb scrn recrds
G9933 0010 3 Adenoma(s) or colorectal cancer detected during screening colonoscopy Canc detectd during col scrn
G9934 0010 3 Documentation that neoplasm detected is only diagnosed as traditional serrated adenoma, sessile serrated polyp, or sessile serrated adenoma Doc rsn not detecting cancer
G9935 0010 3 Adenoma(s) or colorectal cancer not detected during screening colonoscopy Canc not detectd during srcn
G9936 0010 3 Surveillance colonoscopy - personal history of colonic polyps, colon cancer, or other malignant neoplasm of rectum, rectosigmoid junction, and anus Pmh plyp/neo co/rect/jun/ans
G9937 0010 3 Diagnostic colonoscopy Dig or surv colsco
G9938 0010 3 Patients age 66 or older in institutional special needs plans (snp) or residing in long-term care with pos code 32, 33, 34, 54, or 56 for more than 90 days during the measurement period Pt 66+ snp or ltc pos
G9939 0010 3 Pathologists/dermatopathologists is the same clinician who performed the biopsy Same path/derm perf biopsy
G9940 0010 3 Documentation of medical reason(s) for not on a statin (e.g., pregnancy, in vitro fertilization, clomiphene rx, esrd, cirrhosis, muscular pain and disease during the measurement period or prior year) Doc reas no statin therapy
G9941 0010 3 Back pain was measured by the visual analog scale (vas) within three months preoperatively and at three months (6 - 20 weeks) postoperatively Pre and post vas wthn 3 mos
G9942 0010 3 Patient had any additional spine procedures performed on the same date as the lumbar discectomy/laminectomy Adtl spine proc on same date
G9943 0010 3 Back pain was not measured by the visual analog scale (vas) within three months preoperatively and at three months ( 6 - 20 weeks) postoperatively Bk pn nt msr vas scl pre/pst
G9944 0010 3 Back pain was measured by the visual analog scale (vas) within three months preoperatively and at one year (9 to 15 months) postoperatively Vas 3 mon pre and 1 yr post
G9945 0010 3 Patient had cancer, fracture or infection related to the lumbar spine or patient had idiopathic or congenital scoliosis Pt w/cancer scoliosis
G9946 0010 3 Back pain was not measured by the visual analog scale (vas) within three months preoperatively and at one year (9 to 15 months) postoperatively Bk pain no vas
G9947 0010 3 Leg pain was measured by the visual analog scale (vas) within three months preoperatively and at three months (6 to 20 weeks) postoperatively Pre and post vas wthn 3 mos
G9948 0010 3 Patient had any additional spine procedures performed on the same date as the lumbar discectomy/laminectomy Adtl spine proc on same date
G9949 0010 3 Leg pain was not measured by the visual analog scale (vas) at three months (6 ? 20 weeks) postoperatively Leg pain no vas
G9954 0010 3 Patient exhibits 2 or more risk factors for post-operative vomiting Pt >2 rsk fac post-op vomit
G9955 0010 3 Cases in which an inhalational anesthetic is used only for induction Inhlnt anesth only for induc
G9956 0010 3 Patient received combination therapy consisting of at least two prophylactic pharmacologic anti-emetic agents of different classes preoperatively and/or intraoperatively Combo thrpy of >= 2 prophly
G9957 0010 3 Documentation of medical reason for not receiving combination therapy consisting of at least two prophylactic pharmacologic anti-emetic agents of different classes preoperatively and/or intraoperatively (e.g., intolerance or other medical reason) Doc med rsn no combo thrpy
G9958 0010 3 Patient did not receive combination therapy consisting of at least two prophylactic pharmacologic anti-emetic agents of different classes preoperatively and/or intraoperatively No combo prohpyl thrp for pt
G9959 0010 3 Systemic antimicrobials not prescribed Systemic antimicro not presc
G9960 0010 3 Documentation of medical reason(s) for prescribing systemic antimicrobials Med rsn sys antimi nt rx
G9961 0010 3 Systemic antimicrobials prescribed Systemic antimicro presc
G9962 0010 3 Embolization endpoints are documented separately for each embolized vessel and ovarian artery angiography or embolization performed in the presence of variant uterine artery anatomy Embolization doc separatly
G9963 0010 3 Embolization endpoints are not documented separately for each embolized vessel or ovarian artery angiography or embolization not performed in the presence of variant uterine artery anatomy Embolization not doc separat
G9964 0010 3 Patient received at least one well-child visit with a pcp during the performance period Pt recv >=1 well-chld visit
G9965 0010 3 Patient did not receive at least one well-child visit with a pcp during the performance period No well-chld vist recv by pt
G9966 0010 3 Children who were screened for risk of developmental, behavioral and social delays using a standardized tool with interpretation and report Scrn, inter, report child
G9967 0010 3 Children who were not screened for risk of developmental, behavioral and social delays using a standardized tool with interpretation and report No scrn, inter, reprt child
G9968 0010 3 Patient was referred to another provider or specialist during the performance period Pt refrd 2 pvdr/spclst in pp
G9969 0010 3 Provider who referred the patient to another provider received a report from the provider to whom the patient was referred Pvdr rfrd pt rprt rcvd
G9970 0010 3 Provider who referred the patient to another provider did not receive a report from the provider to whom the patient was referred Pvdr rfrd pt no rprt rcvd
G9974 0010 3 Dilated macular exam performed, including documentation of the presence or absence of macular thickening or geographic atrophy or hemorrhage and the level of macular degeneration severity Mac exam perf
G9975 0010 3 Documentation of medical reason(s) for not performing a dilated macular examination Doc med rsn no dil mac exam
G9978 0010 3 Remote in-home visit for the evaluation and management of a new patient for use only in a medicare-approved bundled payments for care improvement advanced (bpci advanced) model episode of care, which requires these 3 key components: a problem focused history; a problem focused examination; and straightforward medical decision making, furnished in real time using interactive audio and video technology. counseling and coordination of care with other physicians, other qualified health care professionals or agencies are provided consistent with the nature of the problem(s) and the needs of the patient or the family or both. usually, the presenting problem(s) are self limited or minor. typically, 10 minutes are spent with the patient or family or both via real time, audio and video intercommunications technology Remote e/m new pt 10mins
G9979 0010 3 Remote in-home visit for the evaluation and management of a new patient for use only in a medicare-approved bundled payments for care improvement advanced (bpci advanced) model episode of care, which requires these 3 key components: an expanded problem focused history; an expanded problem focused examination; straightforward medical decision making, furnished in real time using interactive audio and video technology. counseling and coordination of care with other physicians, other qualified health care professionals or agencies are provided consistent with the nature of the problem(s) and the needs of the patient or the family or both. usually, the presenting problem(s) are of low to moderate severity. typically, 20 minutes are spent with the patient or family or both via real time, audio and video intercommunications technology Remote e/m new pt 20mins
G9980 0010 3 Remote in-home visit for the evaluation and management of a new patient for use only in a medicare-approved bundled payments for care improvement advanced (bpci advanced) model episode of care, which requires these 3 key components: a detailed history; a detailed examination; medical decision making of low complexity, furnished in real time using interactive audio and video technology. counseling and coordination of care with other physicians, other qualified health care professionals or agencies are provided consistent with the nature of the problem(s) and the needs of the patient or the family or both. usually, the presenting problem(s) are of moderate severity. typically, 30 minutes are spent with the patient or family or both via real time, audio and video intercommunications technology Remote e/m new pt 30 mins
G9981 0010 3 Remote in-home visit for the evaluation and management of a new patient for use only in a medicare-approved bundled payments for care improvement advanced (bpci advanced) model episode of care, which requires these 3 key components: a comprehensive history; a comprehensive examination; medical decision making of moderate complexity, furnished in real time using interactive audio and video technology. counseling and coordination of care with other physicians, other qualified health care professionals or agencies are provided consistent with the nature of the problem(s) and the needs of the patient or the family or both. usually, the presenting problem(s) are of moderate to high severity. typically, 45 minutes are spent with the patient or family or both via real time, audio and video intercommunications technology Remote e/m new pt 45mins
G9982 0010 3 Remote in-home visit for the evaluation and management of a new patient for use only in a medicare-approved bundled payments for care improvement advanced (bpci advanced) model episode of care, which requires these 3 key components: a comprehensive history; a comprehensive examination; medical decision making of high complexity, furnished in real time using interactive audio and video technology. counseling and coordination of care with other physicians, other qualified health care professionals or agencies are provided consistent with the nature of the problem(s) and the needs of the patient or the family or both. usually, the presenting problem(s) are of moderate to high severity. typically, 60 minutes are spent with the patient or family or both via real time, audio and video intercommunications technology Remote e/m new pt 60mins
G9983 0010 3 Remote in-home visit for the evaluation and management of an established patient for use only in a medicare-approved bundled payments for care improvement advanced (bpci advanced) model episode of care, which requires at least 2 of the following 3 key components: a problem focused history; a problem focused examination; straightforward medical decision making, furnished in real time using interactive audio and video technology. counseling and coordination of care with other physicians, other qualified health care professionals or agencies are provided consistent with the nature of the problem(s) and the needs of the patient or the family or both. usually, the presenting problem(s) are self limited or minor. typically, 10 minutes are spent with the patient or family or both via real time, audio and video intercommunications technology Remote e/m est. pt 10mins
G9984 0010 3 Remote in-home visit for the evaluation and management of an established patient for use only in a medicare-approved bundled payments for care improvement advanced (bpci advanced) model episode of care, which requires at least 2 of the following 3 key components: an expanded problem focused history; an expanded problem focused examination; medical decision making of low complexity, furnished in real time using interactive audio and video technology. counseling and coordination of care with other physicians, other qualified health care professionals or agencies are provided consistent with the nature of the problem(s) and the needs of the patient or the family or both. usually, the presenting problem(s) are of low to moderate severity. typically, 15 minutes are spent with the patient or family or both via real time, audio and video intercommunications technology Remote e/m est. pt 15mins
G9985 0010 3 Remote in-home visit for the evaluation and management of an established patient for use only in a medicare-approved bundled payments for care improvement advanced (bpci advanced) model episode of care, which requires at least 2 of the following 3 key components: a detailed history; a detailed examination; medical decision making of moderate complexity, furnished in real time using interactive audio and video technology. counseling and coordination of care with other physicians, other qualified health care professionals or agencies are provided consistent with the nature of the problem(s) and the needs of the patient or the family or both. usually, the presenting problem(s) are of moderate to high severity. typically, 25 minutes are spent with the patient or family or both via real time, audio and video intercommunications technology Remote e/m est. pt 25mins
G9986 0010 3 Remote in-home visit for the evaluation and management of an established patient for use only in a medicare-approved bundled payments for care improvement advanced (bpci advanced) model episode of care, which requires at least 2 of the following 3 key components: a comprehensive history; a comprehensive examination; medical decision making of high complexity, furnished in real time using interactive audio and video technology. counseling and coordination of care with other physicians, other qualified health care professionals or agencies are provided consistent with the nature of the problem(s) and the needs of the patient or the family or both. usually, the presenting problem(s) are of moderate to high severity. typically, 40 minutes are spent with the patient or family or both via real time, audio and video intercommunications technology Remote e/m est. pt 40mins
G9987 0010 3 Bundled payments for care improvement advanced (bpci advanced) model home visit for patient assessment performed by clinical staff for an individual not considered homebound, including, but not necessarily limited to patient assessment of clinical status, safety/fall prevention, functional status/ambulation, medication reconciliation/management, compliance with orders/plan of care, performance of activities of daily living, and ensuring beneficiary connections to community and other services; for use only for a bpci advanced model episode of care; may not be billed for a 30-day period covered by a transitional care management code Bpci advanced in home visit