Home / HCPCS / M codes

HCPCS M codes: Medical services

451 active HCPCS Level II codes beginning with M, from the CMS October 2026 quarterly file. "Added" is the year the code first appeared in the HCPCS file.

CodeLong descriptionShort descriptionAdded
M0001Advancing cancer care mips value pathwaysAdvancing cancer care mvp2023
M0002Optimal care for kidney health mips value pathwaysOpt care kidney hlth mvp2023
M0004Quality care for patients with neurological conditions mips value pathwayQual care neurologic cnd mvp2023
M0005Value in primary care mips value pathwayValue in primary care mvp2023
M0010Enhancing oncology model (eom) monthly enhanced oncology services (meos) payment for eom enhanced servicesEom meos payment2023
M0075Cellular therapyCellular therapy1986
M0076ProlotherapyProlotherapy1986
M0100Intragastric hypothermia using gastric freezingIntragastric hypothermia1986
M0201Administration of pneumococcal, influenza, hepatitis b, and/or covid-19 vaccine inside a patient's home; reported only once per individual home per date of service when such vaccine administration(s) are performed at the patient's homePne flu hepb cov home admin2021
M0224Intravenous infusion, pemivibart, for the pre-exposure prophylaxis only, for certain adults and adolescents (12 years of age and older weighing at least 40 kg) with no known sars-cov-2 exposure, who either have moderate-to-severe immune compromise due to a medical condition or receipt of immunosuppressive medications or treatments, includes infusion and post administration monitoringPemivibart infusion2024
M0231Intravenous infusion, tocilizumabbavi, for hospitalized adult patients with covid-19 who are receiving systemic corticosteroids and require supplemental oxygen, non-invasive or invasive mechanical ventilation, or extracorporeal membrane oxygenation only, includes infusion and post administration monitoring, first doseInf tocilizumab-bavi 1st dos2026
M0232Intravenous infusion, tocilizumabbavi, for hospitalized adult patients with covid-19 who are receiving systemic corticosteroids and require supplemental oxygen, non-invasive or invasive mechanical ventilation, or extracorporeal membrane oxygenation only, includes infusion and post administration monitoring, second doseInf tocilizumab-bavi 2nd dos2026
M0233Intravenous infusion, tocilizumab-aazg, for hospitalized adult patients with covid-19 who are receiving systemic corticosteroids and require supplemental oxygen, non-invasive or invasive mechanical ventilation, or extracorporeal membrane oxygenation (ecmo) only, includes infusion and post administration monitoring, first doseIntra inf, toci, first dose2026
M0234Intravenous infusion, tocilizumab-aazg, for hospitalized adult patients with covid-19 who are receiving systemic corticosteroids and require supplemental oxygen, non-invasive or invasive mechanical ventilation, or extracorporeal membrane oxygenation (ecmo) only, includes infusion and post administration monitoring, second doseIntra inf, toci, second dos2026
M0235Intravenous infusion, monoclonal antibody products with an indication for post-exposure prophylaxis or treatment of covid-19, for hospitalized adults and/or pediatric patients who are receiving systemic corticosteroids and require supplemental oxygen, non-invasive or invasive mechanical ventilation, or extracorporeal membrane oxygenation (ecmo) only, includes infusion and post administration monitoring, not otherwise classified, first doseIntrav inf, mon anti, fir do2025
M0236Intravenous infusion, monoclonal antibody products with an indication for post-exposure prophylaxis or treatment of covid-19, for hospitalized adults and/or pediatric patients who are receiving systemic corticosteroids and require supplemental oxygen, non-invasive or invasive mechanical ventilation, or extracorporeal membrane oxygenation (ecmo) only, includes infusion and post administration monitoring, not otherwise classified, second doseIntrav inf, mon anti, sec do2025
M0237Intravenous infusion, tocilizumab-anoh, for hospitalized adult patients with covid-19 who are receiving systemic corticosteroids and require supplemental oxygen, non-invasive or invasive mechanical ventilation, or extracorporeal membrane oxygenation (ecmo) only, includes infusion and post administration monitoring, first doseIntrav inf, toci, first dose2025
M0238Intravenous infusion, tocilizumab-anoh, for hospitalized adult patients with covid-19 who are receiving systemic corticosteroids and require supplemental oxygen, non-invasive or invasive mechanical ventilation, or extracorporeal membrane oxygenation (ecmo) only, includes infusion and post administration monitoring, second doseIntrav inf, toci, second dos2025
M0249Intravenous infusion, tocilizumab, for hospitalized adults and pediatric patients (2 years of age and older) with covid-19 who are receiving systemic corticosteroids and require supplemental oxygen, non-invasive or invasive mechanical ventilation, or extracorporeal membrane oxygenation (ecmo) only, includes infusion and post administration monitoring, first doseAdm tocilizu covid-19 1st2021
M0250Intravenous infusion, tocilizumab, for hospitalized adults and pediatric patients (2 years of age and older) with covid-19 who are receiving systemic corticosteroids and require supplemental oxygen, non-invasive or invasive mechanical ventilation, or extracorporeal membrane oxygenation (ecmo) only, includes infusion and post administration monitoring, second doseAdm tocilizu covid-19 2nd2021
M0300Iv chelation therapy (chemical endarterectomy)Iv chelationtherapy1986
M0301Fabric wrapping of abdominal aneurysmFabric wrapping of aneurysm1986
M1003Tb screening performed and results interpreted within twelve months prior to initiation of first-time biologic and/or immune response modifier therapyTb scr 12 mo pri fst bio dz2019
M1004Documentation of medical reason for not screening for tb or interpreting results (i.e., patient positive for tb and documentation of past treatment; patient who has recently completed a course of anti-tb therapy)Doc med rsn no srn tb2019
M1005Tb screening not performed or results not interpreted, reason not givenTb scr no perf2019
M1006Disease activity not assessed, reason not givenDz not ases, no rsn2019
M1007>=50% of total number of a patient's outpatient ra encounters assessed>=50% total pt outpt ra enct2019
M1008<50% of total number of a patient's outpatient ra encounters assessed<50% total pt outpt ra encts2019
M1009Discharge/discontinuation of the episode of care documented in the medical recordDc eoc doc med rec2019
M1010Discharge/discontinuation of the episode of care documented in the medical recordDc eoc doc med rec2019
M1011Discharge/discontinuation of the episode of care documented in the medical recordDc eoc doc med rec2019
M1012Discharge/discontinuation of the episode of care documented in the medical recordDc eoc doc med rec2019
M1013Discharge/discontinuation of the episode of care documented in the medical recordDc eoc doc med rec2019
M1014Discharge/discontinuation of the episode of care documented in the medical recordDc epi care doc medrec2019
M1016Female patients unable to bear childrenPt dx meop or sur steri2019
M1018Patients with an active diagnosis or history of cancer (except basal cell and squamous cell skin carcinoma), patients who are heavy tobacco smokers, lung cancer screening patientsPt dx hst cr pt sk lg cr scr2019
M1019Adolescent patients 12 to 17 years of age 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 5Adl pt mj dep ds rs 12 phq<52019
M1020Adolescent patients 12 to 17 years of age 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 5Adl pt mj dep ds no rs 12 mo2019
M1021Patient had only urgent care visits during the performance periodPt uc in pp2019
M1027Imaging of the head (ct or mri) was obtainedImg head (ct or mri) obtnd2019
M1028Documentation of patients with primary headache diagnosis and imaging other than ct or mri obtainedDoc of pt prm hda dx and otr2019
M1029Imaging of the head (ct or mri) was not obtained, reason not givenDoc sysm rsn img hd2019
M1032Adults currently taking pharmacotherapy for oudAdt tkng pharmthry for oud2019
M1034Adults who have at least 180 days of continuous pharmacotherapy with a medication prescribed for oud without a gap of more than seven daysAdt 180 dys pharmthry oud2019
M1035Adults who are deliberately phased out of medication assisted treatment (mat) prior to 180 days of continuous treatmentAdt pd out mat pr 180 dys tx2019
M1036Adults who have not had at least 180 days of continuous pharmacotherapy with a medication prescribed for oud without a gap of more than seven daysAdt no 180 dys pharmthry oud2019
M1037Patients with a diagnosis of lumbar spine region cancer at the time of the procedurePt dx lum sp reg cacr2019
M1038Patients with a diagnosis of lumbar spine region fracture at the time of the procedurePt dx lum sp reg fract2019
M1039Patients with a diagnosis of lumbar spine region infection at the time of the procedurePt dx lum sp reg inf2019
M1040Patients with a diagnosis of lumbar idiopathic or congenital scoliosisPt dx lum idi or cong scol2019
M1041Patient had cancer, acute fracture or infection related to the lumbar spine or patient had neuromuscular, idiopathic or congenital lumbar scoliosisPt cr ft inf lm or pt id sl2019
M1043Functional status was not measured by the oswestry disability index (odi version 2.1a) at one year (9 to 15 months) postoperativelyFs no odi 9-15mo2019
M1045Functional status measured by the oxford knee score (oks) at one year (9 to 15 months) postoperatively was greater than or equal to 37 or knee injury and osteoarthritis outcome score joint replacement (koos, jr.) was greater than or equal to 71Fs oks 9-15mo >= 37 >= 712019
M1046Functional status measured by the oxford knee score (oks) at one year (9 to 15 months) postoperatively was less than 37 or the knee injury and osteoarthritis outcome score joint replacement (koos, jr.) was less than 71 postoperativelyFs oks 9-15mo < 37 < 712019
M1049Functional status was not measured by the oswestry disability index (odi version 2.1a) at three months (6 - 20 weeks) postoperativelyFs wth scr no odi pre and p2019
M1051Patient had cancer, acute fracture or infection related to the lumbar spine or patient had neuromuscular, idiopathic or congenital lumbar scoliosisPt w/cancer scoliosis2019
M1052Leg pain was not measured by the visual analog scale (vas) or numeric pain scale at one year (9 to 15 months) postoperativelyLg pn not meas w/ vas 1yr po2019
M1054Patient had only urgent care visits during the performance periodPt uc in pp2019
M1055Aspirin or another antiplatelet therapy usedAspirin used2019
M1056Prescribed anticoagulant medication during the performance period, history of gi bleeding, history of intracranial bleeding, bleeding disorder and specific provider documented reasons: allergy to aspirin or anti-platelets, use of non-steroidal anti-inflammatory agents, drug-drug interaction, uncontrolled hypertension > 180/110 mmhg or gastroesophageal reflux diseasePresc antico med in pp2019
M1057Aspirin or another antiplatelet therapy not used, reason not givenAspirin not used, no rsn2019
M1058Patient was a permanent nursing home resident at any time during the performance periodPt prm nurs hm res in pp2019
M1059Patient was in hospice or receiving palliative care at any time during the performance periodPt no prm nurs hm res in pp2019
M1060Patient died prior to the end of the performance periodPt died in pp2019
M1067Hospice services for patient provided any time during the measurement periodHspc pt prv time meam per2019
M1068Adults who are not ambulatoryPt not ambulatory2019
M1069Patient screened for future fall riskPt scr ft fall rsk2019
M1070Patient not screened for future fall risk, reason not givenPt not scrn fut fall no rsn2019
M1106The start of an episode of care documented in the medical recordStart eoc doc med rec2020
M1107Documentation stating patient has a diagnosis of a degenerative neurological condition such as als, ms, or parkinson's diagnosed at any time before or during the episode of careDocu dx degen neuro2020
M1108Ongoing care not clinically indicated because the patient needed a home program only, referral to another provider or facility, or consultation only, as documented in the medical recordOc ni pt home prog2020
M1109Ongoing care not medically possible because the patient was discharged early due to specific medical events, documented in the medical record, such as the patient became hospitalized or scheduled for surgeryOc ni pt dc2020
M1110Ongoing care not possible because the patient self-discharged early (e.g., financial or insurance reasons, transportation problems, or reason unknown)Oc not p pt selfdc2020
M1111The start of an episode of care documented in the medical recordStart eoc doc med rec2020
M1112Documentation stating patient has a diagnosis of a degenerative neurological condition such as als, ms, or parkinson's diagnosed at any time before or during the episode of careDocu dx degen neuro2020
M1113Ongoing care not clinically indicated because the patient needed a home program only, referral to another provider or facility, or consultation only, as documented in the medical recordOc ni pt home prog2020
M1114Ongoing care not medically possible because the patient was discharged early due to specific medical events, documented in the medical record, such as the patient became hospitalized or scheduled for surgeryOc ni pt dc2020
M1115Ongoing care not possible because the patient self-discharged early (e.g., financial or insurance reasons, transportation problems, or reason unknown)Oc ni pt selfdc2020
M1116The start of an episode of care documented in the medical recordStart eoc doc med rec2020
M1117Documentation stating patient has a diagnosis of a degenerative neurological condition such as als, ms, or parkinson's diagnosed at any time before or during the episode of careDocu dx degen neuro2020
M1118Ongoing care not clinically indicated because the patient needed a home program only, referral to another provider or facility, or consultation only, as documented in the medical recordOc ni pt home prog2020
M1119Ongoing care not medically possible because the patient was discharged early due to specific medical events, documented in the medical record, such as the patient became hospitalized or scheduled for surgeryOc ni pt dc2020
M1120Ongoing care not possible because the patient self-discharged early (e.g., financial or insurance reasons, transportation problems, or reason unknown)Oc ni pt selfdc2020
M1121The start of an episode of care documented in the medical recordStart eoc doc med rec2020
M1122Documentation stating patient has a diagnosis of a degenerative neurological condition such as als, ms, or parkinson's diagnosed at any time before or during the episode of careDocu dx degen neuro2020
M1123Ongoing care not clinically indicated because the patient needed a home program only, referral to another provider or facility, or consultation only, as documented in the medical recordOc ni pt home prog2020
M1124Ongoing care not medically possible because the patient was discharged early due to specific medical events, documented in the medical record, such as the patient became hospitalized or scheduled for surgeryOc ni pt dc 1-2 vis2020
M1125Ongoing care not possible because the patient self-discharged early (e.g., financial or insurance reasons, transportation problems, or reason unknown)Oc ni pt selfdc 1-2 vis2020
M1126The start of an episode of care documented in the medical recordStart eoc doc med rec2020
M1127Documentation stating patient has a diagnosis of a degenerative neurological condition such as als, ms, or parkinson's diagnosed at any time before or during the episode of careDocu dx degen neuro2020
M1128Ongoing care not clinically indicated because the patient needed a home program only, referral to another provider or facility, or consultation only, as documented in the medical recordOc ni pt home prog2020
M1129Ongoing care not medically possible because the patient was discharged early due to specific medical events, documented in the medical record, such as the patient became hospitalized or scheduled for surgeryOc ni pt dc2020
M1130Ongoing care not possible because the patient self-discharged early (e.g., financial or insurance reasons, transportation problems, or reason unknown)Oc ni pt selfdc2020
M1131Documentation stating patient has a diagnosis of a degenerative neurological condition such as als, ms, or parkinson's diagnosed at any time before or during the episode of careDocu dx degen neuro2020
M1132Ongoing care not clinically indicated because the patient needed a home program only, referral to another provider or facility, or consultation only, as documented in the medical recordOc ni pt home prog2020
M1133Ongoing care not medically possible because the patient was discharged early due to specific medical events, documented in the medical record, such as the patient became hospitalized or scheduled for surgeryOc ni pt dc2020
M1134Ongoing care not possible because the patient self-discharged early (e.g., financial or insurance reasons, transportation problems, or reason unknown)Oc ni pt selfdc2020
M1135The start of an episode of care documented in the medical recordStart eoc doc med rec2020
M1141Functional status was not measured by the oxford knee score (oks) or the knee injury and osteoarthritis outcome score joint replacement (koos, jr.) at one year (9 to 15 months) postoperativelyFs no oks2020
M1142Emergent casesEmerge cases2020
M1143Initiated episode of rehabilitation therapy, medical, or chiropractic care for neck impairmentNi rehab med chiro2020
M1146Ongoing care not clinically indicated because the patient needed a home program only, referral to another provider or facility, or consultation only, as documented in the medical recordOngoing care not ind2021
M1147Ongoing care not medically possible because the patient was discharged early due to specific medical events, documented in the medical record, such as the patient became hospitalized or scheduled for surgeryCare not poss med rsn2021
M1148Ongoing care not possible because the patient self-discharged early (e.g., financial or insurance reasons, transportation problems, or reason unknown)Pt self dschg2021
M1149Patient unable to complete the neck fs prom at initial evaluation and/or discharge due to blindness, illiteracy, severe mental incapacity or language incompatibility, and an adequate proxy is not availableNo neck fs prom incap2021
M1150Current or prior left ventricular ejection fraction (lvef) less than or equal to 40% or documentation of moderately or severely depressed left ventricular systolic functionLvef <=40% or mod/sev l vsf2023
M1151Patients with a history of heart transplant or with a left ventricular assist device (lvad)Pt w/ hx trnsplt or lvad2023
M1152Patients with a history of heart transplant or with a left ventricular assist device (lvad)Pt w/ hx trnsplt or lvad2023
M1153Patient with diagnosis of osteoporosis on date of encounterPt w/ dx osteo doe2023
M1159Hospice services provided to patient any time during the measurement periodHospc serv dur meas pd2023
M1160Patient had anaphylaxis due to the meningococcal vaccine any time on or before the patient's 13th birthdayPt anphx due to mengb bef 132023
M1161Patient had anaphylaxis due to the tetanus, diphtheria or pertussis vaccine any time on or before the patient's 13th birthdayPt anphx due to dtp bef 132023
M1162Patient had encephalitis due to the tetanus, diphtheria or pertussis vaccine any time on or before the patient's 13th birthdayPt enceph due to dtp bef 132023
M1163Patient had anaphylaxis due to the hpv vaccine any time on or before the patient's 13th birthdayPt anphx due to hpv bef 132023
M1164Patients with dementia any time during the patient's history through the end of the measurement periodPt w/ dementia any time2023
M1165Patients who use hospice services any time during the measurement periodPt use hspc dur meas pd2023
M1166Pathology report for tissue specimens produced from wide local excisions or re-excisionsPath rpt tis spec wle/reexc2023
M1167In hospice or using hospice services during the measurement periodHspc dur meas pd2023
M1168Patient received an influenza vaccine on or between july 1 of the year prior to the measurement period and june 30 of the measurement periodPt recd flu vax 7/1-6/302023
M1169Documentation of medical reason(s) for not administering influenza vaccine (e.g., prior anaphylaxis due to the influenza vaccine)Doc med rsn no flu vax2023
M1170Patient 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 periodPt w/o flu vax 7/1-6/302023
M1171Patient received at least one td vaccine or one tdap vaccine between nine years prior to the encounter and the end of the measurement periodPt recd 1 td/tdap 9yrs prior2023
M1172Documentation of medical reason(s) for not administering td or tdap vaccine (e.g., prior anaphylaxis due to the td or tdap vaccine or history of encephalopathy within seven days after a previous dose of a td-containing vaccine)Doc med rsn no td/tdap2023
M1173Patient did not receive at least one td vaccine or one tdap vaccine between nine years prior to the encounter and the end of the measurement periodPt no rec td/tdap 9yrs prior2023
M1174Patient received at least two doses of the herpes zoster recombinant vaccine (at least 28 days apart) on october 20, 2017, through the end of the measurement periodPt w/ 2 hzv 10/2017 - mp2023
M1175Documentation of medical reason(s) for not administering zoster vaccine (e.g., prior anaphylaxis due to the zoster vaccine)Doc med rsn no hzv2023
M1176Patient did not receive two doses of the herpes zoster recombinant vaccine (at least 28 days apart) on october 20, 2017, through the end of the measurement periodNo 2 hzv 10/2017-meas pd2023
M1177Patient received any pneumococcal conjugate or polysaccharide vaccine on or after their 19th birthday and before the end of the measurement periodPt recd pcv on/aft 192023
M1178Documentation of medical reason(s) for not administering pneumococcal vaccine (e.g., prior anaphylaxis due to the pneumococcal vaccine)Doc med rsn no pcv2023
M1179Patient did not receive any pneumococcal conjugate or polysaccharide vaccine, on or after their 19th birthday and before or during measurement periodNo pcv recd2023
M1180Patients on immune checkpoint inhibitor therapyPt imm ckpt inhib therapy2023
M1181Grade 2 or above diarrhea and/or grade 2 or above colitisGr 2 or> dia or gr2 or> col2023
M1182Patients not eligible due to pre-existing inflammatory bowel disease (ibd) (e.g., ulcerative colitis, crohn's disease)Not elg pre ex ibd/uc/crohn2023
M1183Documentation of immune checkpoint inhibitor therapy held and corticosteroids or immunosuppressants prescribed or administeredDoc imm ckpt inhib hld2023
M1184Documentation of medical reason(s) for not prescribing or administering corticosteroid or immunosuppressant treatment (e.g., allergy, intolerance, infectious etiology, pancreatic insufficiency, hyperthyroidism, prior bowel surgical interventions, celiac disease, receiving other medication, awaiting diagnostic workup results for alternative etiologies, other medical reasons/contraindication)Doc med rsn no cst/ist rx2023
M1185Documentation of immune checkpoint inhibitor therapy not held and/or corticosteroids or immunosuppressants prescribed or administered was not performed, reason not givenImm ckpt inhib not hld no rx2023
M1186Patients who have an order for or are receiving hospice or palliative carePt w/ rx for hspc/plltv care2023
M1187Patients with a diagnosis of end stage renal disease (esrd)Pt w/ esrd2023
M1188Patients with a diagnosis of chronic kidney disease (ckd) stage 5Pt w/ ckd stg 52023
M1189Documentation of a kidney health evaluation defined by an estimated glomerular filtration rate (egfr) and urine albumin-creatinine ratio (uacr) performedDoc khe pef w/efgr/uacr2023
M1190Documentation of a kidney health evaluation was not performed or defined by an estimated glomerular filtration rate (egfr) and urine albumin-creatinine ratio (uacr)Doc khe not pef w/efgr/uacr2023
M1191Hospice services provided to patient any time during the measurement periodHspc svc any time in meas pd2023
M1192Patients with an existing diagnosis of squamous cell carcinoma of the esophagusPt w/ dx sq cell ca of esoph2023
M1193Surgical pathology reports that contain impression or conclusion of or recommendation for testing of mmr by immunohistochemistry, msi by dna-based testing status, or bothRpts w/ imp/con mmr/msi2023
M1194Documentation of medical reason(s) surgical pathology reports did not contain impression or conclusion of or recommendation for testing of mmr by immunohistochemistry, msi by dna-based testing status, or both tests were not included (e.g., patient will not be treated with checkpoint inhibitor therapy, no residual carcinoma is present in the sample [tissue exhausted or status post neoadjuvant treatment], insufficient tumor for testing)Med rsn no imp/con mmr/msi2023
M1195Surgical pathology reports that do not contain impression or conclusion of or recommendation for testing of mmr by immunohistochemistry, msi by dna-based testing status, or both, reason not givenRpt wo imp/con mmr/msi2023
M1196Initial (index visit) numeric rating scale (nrs), visual rating scale (vrs), or itchyquant assessment score of greater than or equal to 4Ixv nrs vrs iqa >=42023
M1197Itch severity assessment score is reduced by 3 or more points from the initial (index) assessment score to the follow-up visit scoreIsa reduced >=3 fr ixv2023
M1198Itch severity assessment score was not reduced by at least 3 points from initial (index) score to the follow-up visit score or assessment was not completed during the follow-up encounterIsa not red 3pts /no assess2023
M1199Patients receiving rrtPt rec'g rrt2023
M1200Ace inhibitor (ace-i) or arb therapy prescribed during the measurement periodAce-i/arb rx2023
M1201Documentation of medical reason(s) for not prescribing ace inhibitor (ace-i) or arb therapy during the measurement period (e.g., pregnancy, history of angioedema to ace-i, other allergy to ace-i and arb, hyperkalemia or history of hyperkalemia while on ace-i or arb therapy, acute kidney injury due to ace-i or arb therapy), other medical reasons)Med rsn no ace-i/arb rx2023
M1202Documentation of patient reason(s) for not prescribing ace inhibitor or arb therapy during the measurement period, (e.g., patient declined, other patient reasons)Pt rsn no ace-i/arb rx2023
M1203Ace inhibitor or arb therapy not prescribed during the measurement period, reason not givenNo rsn ace-i/arb rx2023
M1204Initial (index visit) numeric rating scale (nrs), visual rating scale (vrs), or itchyquant assessment score of greater than or equal to 4Ixv nrs vrs iqa >=42023
M1205Itch severity assessment score is reduced by 3 or more points from the initial (index) assessment score to the follow-up visit scoreIsa reduced >=32023
M1206Itch severity assessment score was not reduced by at least 3 points from initial (index) score to the follow-up visit score or assessment was not completed during the follow-up encounterIsa not red 3pts/no assess2023
M1207Patient is screened for food insecurity, housing instability, transportation needs, utility difficulties, and interpersonal safetyPt scrn sdoh2023
M1208Patient is not screened for food insecurity, housing instability, transportation needs, utility difficulties, and interpersonal safetyPt no scrn sdoh2023
M1209At least two orders for high-risk medications from the same drug class, (table 4), without appropriate diagnoses>=2 same hi-rsk med w/o diag2023
M1210At least two orders for high-risk medications from the same drug class, (table 4), not ordered>=2 same meds tbl4 not ord2023
M1211Most recent glycemic status assessment (hba1c or gmi) level > 9.0%Gsa level>9.0%2024
M1212Glycemic status assessment (hba1c or gmi) level is missing, or was not performed during the measurement periodMissing gsa not perf2024
M1213No history of spirometry results with confirmed airflow obstruction (fev1/fvc < 70%) and present spirometry is >= 70%No hx spiro prs spiro>=70%2024
M1214Spirometry results with confirmed airflow obstruction (fev1/fvc < 70%) documented and reviewedSpiro results wth obs doc2024
M1215Documentation of medical reason(s) for not documenting and reviewing spirometry results (e.g., patients with dementia or tracheostomy)Med rsn for no doc spiro2024
M1216No spirometry results with confirmed airflow obstruction (fev1/fvc < 70%) documented and/or no spirometry performed with results documented during the encounterNo spiro doc no res doc2024
M1217Documentation of system reason(s) for not documenting and reviewing spirometry results (e.g., spirometry equipment not available at the time of the encounter)Sys rsn no doc spiro2024
M1218Patient has copd symptoms (e.g., dyspnea, cough/sputum, wheezing)Pt copd symptoms2024
M1220Dilated retinal eye exam with interpretation by an ophthalmologist or optometrist or artificial intelligence (ai) interpretation documented and reviewed; with evidence of retinopathyDre wth interp rtnopthy2024
M1221Dilated retinal eye exam with interpretation by an ophthalmologist or optometrist or artificial intelligence (ai) interpretation documented and reviewed; without evidence of retinopathyDre w/o rtnopthy2024
M1222Glaucoma plan of care not documented, reason not otherwise specifiedGlaucoma pln of care not doc2024
M1223Glaucoma plan of care documentedGlaucoma plan of care doc2024
M1224Intraocular pressure (iop) reduced by a value less than 20% from the pre-intervention levelIop dec <20% from base2024
M1225Intraocular pressure (iop) reduced by a value of greater than or equal to 20% from the pre-intervention levelIop dec>=20% from base2024
M1226Iop measurement not documented, reason not otherwise specifiedIop not doc2024
M1227Evidence-based therapy was prescribedEb therapy prescribed2024
M1228Patient, who has a reactive hcv antibody test, and has a follow up hcv viral test that detected hcv viremia, has hcv treatment initiated within 3 months of the reactive hcv antibody testPt + hcv aby +vir w/ rx 3 mo2024
M1229Patient, who has a reactive hcv antibody test, and has a follow up hcv viral test that detected hcv viremia, is referred within 1 month of the reactive hcv antibody test to a clinician who treats hcv infectionPt w/ +hcv +vir ref win 1 mo2024
M1230Patient has a reactive hcv antibody test and does not have a follow up hcv viral test, or patient has a reactive hcv antibody test and has a follow up hcv viral test that detects hcv viremia and is not referred to a clinician who treats hcv infection within 1 month and does not have hcv treatment initiated within 3 months of the reactive hcv antibody test, reason not givenPt hcv rctv aby no f/u tst2024
M1231Patient receives hcv antibody test with nonreactive resultPt hcv tst no reactive res2024
M1232Patient receives hcv antibody test with reactive resultPt hcv tst reactive result2024
M1233Patient does not receive hcv antibody test or patient does receive hcv antibody test but results not documented, reason not givenPt no hcv aby or result2024
M1234Patient has a reactive hcv antibody test, and has a follow up hcv viral test that does not detect hcv viremiaPt hcv rctv aby f/u neg2024
M1235Documentation or patient report of hcv antibody test or hcv rna test which occurred prior to the performance periodDoc pt hcv aby rna tst2024
M1236Baseline mrs > 2Baseline mrs > 22024
M1237Patient reason for not screening for food insecurity, housing instability, transportation needs, utility difficulties, and interpersonal safety (e.g., patient declined or other patient reasons)Pt rsn no scrn2024
M1238Documentation that administration of second recombinant zoster vaccine could not occur during the performance period due to the recommended 2-6 month interval between doses (i.e, first dose received after october 31)Doc 2nd recom hzv 2-6 mo int2024
M1239Patient did not respond to the question of patient felt heard and understood by this provider and teamPt no resp heard2024
M1240Patient did not respond to the question of patient felt this provider and team put my best interests first when making recommendations about my carePt no resp best int2024
M1241Patient did not respond to the question of patient felt this provider and team saw me as a person, not just someone with a medical problemPt no resp seen as person2024
M1242Patient did not respond to the question of patient felt this provider and team understood what is important to me in my lifePt no resp imprt to me2024
M1243Patient provided a response other than "completely true" for the question of patient felt heard and understood by this provider and teamPt othr thn true heard2024
M1244Patient provided a response other than "completely true" for the question of patient felt this provider and team put my best interests first when making recommendations about my carePt othr thn true best int2024
M1245Patient provided a response other than "completely true" for the question of patient felt this provider and team saw me as a person, not just someone with a medical problemPt othr thn true person2024
M1246Patient provided a response other than "completely true" for the question of patient felt this provider and team understood what is important to me in my lifePt othr thn true imprt to me2024
M1247Patient responded "completely true" for the question of patient felt this provider and team put my best interests first when making recommendations about my carePt resp true best int2024
M1248Patient responded "completely true" for the question of patient felt this provider and team saw me as a person, not just someone with a medical problemPt resp true seen as person2024
M1249Patient responded "completely true" for the question of patient felt this provider and team understood what is important to me in my lifePt resp true imprt to me2024
M1250Patient responded as "completely true" for the question of patient felt heard and understood by this provider and teamPt resp true heard2024
M1251Patients for whom a proxy completed the entire hu survey on their behalf for any reason (no patient involvement)Pts proxy cmplt hu surv2024
M1252Patients who did not complete at least one of the four patient experience hu survey items and return the hu survey within 60 days of the ambulatory palliative care visitPts no cmplt hu survey2024
M1253Patients who respond on the patient experience hu survey that they did not receive care by the listed ambulatory palliative care provider in the last 60 days (disavowal)Pts hu surv no amb plltv2024
M1254Patients who were deceased when the hu survey reached themPts deceased prior hu surv2024
M1255Patients who have another reason for visiting the clinic [not prenatal or postpartum care] and have a positive pregnancy test but have not established the clinic as an ob provider (e.g., plan to terminate the pregnancy or seek prenatal services elsewhere)Pts w/ othr rsn vst,+prg tst2024
M1256Prior history of known cvdPrior history of known cvd2024
M1257Cvd risk assessment not performed or incomplete (e.g., cvd risk assessment was not documented), reason not otherwise specifiedCvd risk assess not perf2024
M1258Cvd risk assessment performed, have a documented calculated risk scoreCvd risk assess perf2024
M1259Patient status documented within the first year of initiating dialysisPt stat doc <= 1 yr dialysis2024
M1260Patient status not documented within the first year of initiating dialysisPt not doc <= 1 yr dialysis2024
M1261Patients that were on the kidney or kidney-pancreas waitlist prior to initiation of dialysisPts on wtlist bef dialysis2024
M1262Patients who had a transplant prior to initiation of dialysisPts transplt bef dialysis2024
M1263Patients in hospice on their initiation of dialysis date or during the month of evaluationPts hosp dialysis dt2024
M1265Cms medical evidence form 2728 for dialysis patients: initial form completedCms 2728 completed2024
M1266Patients admitted to a skilled nursing facility (snf)Pts admit snf2024
M1267Patients not observed in active status on any kidney or kidney-pancreas transplant waitlist as of the last day of each month during the measurement periodPt no act kid transplt wtlst2024
M1268Patients observed in active status on any kidney or kidney-pancreas transplant waitlist as of the last day of each month during the measurement periodPt ac stat kid trnsplt wtlst2024
M1269Receiving esrd mcp dialysis services by the provider on the last day of the reporting monthRec'd esrd mcp lst day of mo2024
M1270Patients not on any kidney or kidney-pancreas transplant waitlist as of the last day of each month during the measurement periodPts no kid transplt wtlst2024
M1271Patients with dementia at any time prior to or during the monthPts dem any time/dur mo2024
M1272Patients observed on any kidney or kidney-pancreas transplant waitlist as of the last day of each month during the measurement periodPts kid transplt wtlst2024
M1273Patients who were admitted to a skilled nursing facility (snf) within one year of dialysis initiation according to the cms-2728 formPts snf 1 yr dialysis2024
M1274Patients who were admitted to a skilled nursing facility (snf) during the month of evaluation were excluded from that monthPts snf exl mo2024
M1275Patients determined to be in hospice were excluded from month of evaluation and the remainder of reporting periodPts hosp exl2024
M1276Bmi documented outside normal parameters, no follow-up plan documented, no reason givenCalc bmi out nrm param nof/u2024
M1277Colorectal cancer screening results documented and reviewedColorectal ca screen doc rev2024
M1278Elevated or hypertensive blood pressure reading documented, and the indicated follow-up is documentedPre-htn or htn doc, f/u indc2024
M1279Elevated or hypertensive blood pressure reading documented, indicated follow-up not documented, reason not givenPre-htn/htn, no f/u, not gvn2024
M1280Women 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 mastectomyBilat mast/hx bi /unilat mas2024
M1281Blood pressure reading not documented, reason not givenBp scrn no perf at interval2024
M1282Patient screened for tobacco use and identified as a tobacco non-userPt scrn tbco id as non user2024
M1283Patient screened for tobacco use and identified as a tobacco userPt scrn tbco and id as user2024
M1284Patients 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 consecutive days during the measurement periodPt 66+ snp or ltc pos > 90d2024
M1285Screening, diagnostic, film, digital or digital breast tomosynthesis (3d) mammography results were not documented and reviewed, reason not otherwise specifiedScrn mam perf rslts not doc2024
M1286Bmi is documented as being outside of normal parameters, follow-up plan is not completed for documented medical reasonBmi doc onl fup not cmpltd2024
M1287Bmi is documented below normal parameters and a follow-up plan is documentedCalc bmi blw low param f/u2024
M1288Documented reason for not screening or recommending a follow-up for high blood pressureDoc rsn no hbp scrn or f/u2024
M1289Patient identified as tobacco user did not receive tobacco cessation intervention during the measurement period or in the six months prior to the measurement period (counseling and/or pharmacotherapy)No pt tbco cess interv rng2024
M1290Patient not eligible due to active diagnosis of hypertensionPt not eli d/t act dig htn2024
M1291Patients 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 periodPt 66+ frailty and med dem2024
M1292Patients 66 years of age and older with at least one claim/encounter for frailty during the measurement period and an advanced illness diagnosis during the measurement period or the year prior to the measurement periodPt 66+ frail inpt adv ill2024
M1293Bmi is documented above normal parameters and a follow-up plan is documentedCalc bmi abv up param f/u2024
M1294Normal blood pressure reading documented, follow-up not requiredBp scrn perf rec interval2024
M1295Patients with a diagnosis or past history of total colectomy or colorectal cancerPt hx tot col or colon ca2024
M1296Bmi is documented within normal parameters and no follow-up plan is requiredCalc bmi norm parameters2024
M1297Bmi not documented due to medical reason or patient refusal of height or weight measurementBmi not doc medrsn ptref2024
M1298Documentation of patient pregnancy anytime during the measurement period prior to and including the current encounterDoc pt preg dur msrmt pd2024
M1299Influenza immunization administered or previously receivedFlu immunize order/admin2024
M1300Influenza 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 rea2024
M1301Patient identified as a tobacco user received tobacco cessation intervention during the measurement period or in the six months prior to the measurement period (counseling and/or pharmacotherapy)Pt recv tbco cess interv2024
M1302Screening, diagnostic, film digital or digital breast tomosynthesis (3d) mammography results documented and reviewedScrn mam perf rslts doc2024
M1303Hospice services provided to patient any time during the measurement periodHospc serv dur meas pd2024
M1304Patient did not receive any pneumococcal conjugate or polysaccharide vaccine on or after their 19th birthday and before the end of the measurement periodNo pneum vax admin 19+2024
M1305Patient received any pneumococcal conjugate or polysaccharide vaccine on or after their 19th birthday and before the end of the measurement periodPneum vax admin 19+2024
M1306Patient had anaphylaxis due to the pneumococcal vaccine any time during or before the measurement periodPt anphx due to pneum2024
M1307Documentation stating the patient has received or is currently receiving palliative or hospice careDoc pt pal or hospice2024
M1308Influenza immunization was not administered, reason not givenFlu immunize no admin2024
M1309Palliative care services provided to patient any time during the measurement periodPall serv during meas2024
M1310Patient screened for tobacco use and received tobacco cessation intervention during the measurement period or in the six months prior to the measurement period (counseling, pharmacotherapy, or both), if identified as a tobacco userPt scr tob & cess int2024
M1311Anaphylaxis due to the vaccine on or before the date of the encounterAphlx to vax bef enc2024
M1312Patient not screened for tobacco useNo pt tbco scrn rng2024
M1313Tobacco screening not performed or tobacco cessation intervention not provided during the measurement period or in the six months prior to the measurement periodNo tob scr/cess int2024
M1314Bmi not documented and no reason is givenBmi not calculated2024
M1315Colorectal cancer screening results were not documented and reviewed; reason not otherwise specifiedCrc no doc no rsn2024
M1316Current tobacco non-userTobacco non-user2024
M1317Patients who are counseled on connection with a csp and explicitly opt outPts counsl cpt opt out2024
M1318Patients who did not have documented contact with a csp for at least one of their screened positive hrsns within 60 days after screening or documentation that there was no contact with a cspPts no csp doc contact2024
M1319Patients who had documented contact with a csp for at least one of their screened positive hrsns within 60 days after screeningPts csp doc contact2024
M1320Patients who screened positive for at least 1 of the 5 hrsnsPts scrn + hrsn2024
M1321Patients who were not seen within 7 weeks following the date of injection for follow up or who did not have a documented iop or no plan of care documented if the iop was >25 mm hgPts no 7wk inj,no iop,iop>252024
M1322Patients seen within 7 weeks following the date of injection and are screened for elevated intraocular pressure (iop) with tonometry with documented iop =<25 mm hg for injected eyePts 7wk inj, scrn iop =<252024
M1323Patients seen within 7 weeks following the date of injection and are screened for elevated intraocular pressure (iop) with tonometry with documented iop >25 mm hg and a plan of care was documentedPts 7wk inj, scrn iop >252024
M1324Patients who had an intravitreal or periocular corticosteroid injection (e.g., triamcinolone, preservative-free triamcinolone, dexamethasone, dexamethasone intravitreal implant, or fluocinolone intravitreal implant)Pts intravitreal/pci2024
M1325Patients who were not seen for reasons documented by clinician for patient or medical reasons (e.g., inadequate time for follow-up, patients who received a prior intravitreal or periocular steroid injection within the last six (6) months and had a subsequent iop evaluation with iop <25mm hg within seven (7) weeks of treatment)Doc med rsn not seen2024
M1326Patients with a diagnosis of hypotonyPts dx hypotony2024
M1327Patients who were not appropriately evaluated during the initial exam and/or who were not re-evaluated within 8 weeksPts no eval ini xm no 8 wks2024
M1328Patients with a diagnosis of acute vitreous hemorrhagePts dx acute vitreous hem2024
M1329Patients with a post-operative encounter of the eye with the acute pvd within 2 weeks before the initial encounter or 8 weeks after initial acute pvd encounterPts act pvd 2 wks 8 wks2024
M1330Documentation of patient reason(s) for not having a follow up exam (e.g., inadequate time for follow up)Doc pts rsn no f/u xm2024
M1331Patients who were appropriately evaluated during the initial exam and were re-evaluated no later than 8 weeks from initial examPts eval ini xm 8 wks2024
M1332Patients who were not appropriately evaluated during the initial exam and/or who were not re-evaluated within 2 weeksPts no eval ini xm no 2 wks2024
M1333Acute vitreous hemorrhageAcute vitreous hemorrhage2024
M1334Patients with a post-operative encounter of the eye with the acute pvd within 2 weeks before the initial encounter or 2 weeks after initial acute pvd encounterPts act pvd 2 wks 2 wks2024
M1335Documentation of patient reason(s) for not having a follow up exam (e.g., inadequate time for follow up)Doc pts rsn no f/u xm2024
M1336Patients who were appropriately evaluated during the initial exam and were re-evaluated no later than 2 weeksPts eval ini xm 2 wks2024
M1337Acute pvdAcute pvd2024
M1338Patients who had follow-up assessment 30 to 180 days after the index assessment who did not demonstrate positive improvement or maintenance of functioning scores during the performance periodPt f/u 30-180 dys no + imprv2024
M1339Patients who had follow-up assessment 30 to 180 days after the index assessment who demonstrated positive improvement or maintenance of functioning scores during the performance periodPts f/u 30-180 dys + improv2024
M1340Index assessment completed using the 12-item whodas 2.0 or sds during the denominator identification periodIndx whodas 2.0 or sds2024
M1341Patients who did not have a follow-up assessment or did not have an assessment within 30 to 180 days after the index assessment during the performance periodPt no f/u 30-180 dys2024
M1342Patients who died during the performance periodPts died perf per2024
M1343Patients who are at pam level 4 at baseline or patients who are flagged with extreme straight line response sets on the pam or with excessive missing responsesPt pam lvl 4 base or srt lin2024
M1344Patients who did not have a baseline pam score and/or a second score within 4 to 12 months of baseline pam scoreNo bsln/2nd pam score 4-12mo2024
M1345Patients who had a baseline pam score and a second score within 4 to 12 month of baseline pam scorePt bsln pam, 2nd scr 4-12 mo2024
M1346Patients who did not have a net increase in pam score of at least 6 points within a 4 to 12 month periodNo pam inc 6 pts 4-12 mo2024
M1347Patients who achieved a net increase in pam score of at least 3 points in a 4 to 12 month period (passing)Pt pam incr 3 pt 4-12 mo2024
M1348Patients who achieved a net increase in pam score of at least 6-points in a 4 to 12 month period (excellent)Pam incr 6 pt 4-12 mo2024
M1349Patients who did not have a net increase in pam score of at least 3 points within a 4 to 12 month periodNo pam inc 3 pts 4-12 mo2024
M1350Patients who had a completed suicide safety plan initiated, reviewed or updated in collaboration with their clinician (concurrent or within 24 hours) of the index clinical encounterPt w/ suic saf pln init rev2024
M1351Patients who had a suicide safety plan initiated, reviewed, or updated and reviewed and updated in collaboration with the patient and their clinician concurrent or within 24 hours of clinical encounter and within 120 days after initiationPt cmplt suicd saf pln 120dy2024
M1352Suicidal ideation and/or behavior symptoms based on the c-ssrs or equivalent assessmentSuicd c-ssrs assessment, equ2024
M1353Patients who did not have a completed suicide safety plan initiated, reviewed or updated in collaboration with their clinician (concurrent or within 24 hours) of the index clinical encounterPts no cmplt suicd saf pln2024
M1354Patients who did not have a suicide safety plan initiated, reviewed, or updated or reviewed and updated in collaboration with the patient and their clinician concurrent or within 24 hours of clinical encounter and within 120 days after initiationPt no suicd saf pln 120dy2024
M1355Suicide risk based on their clinician's evaluation or a clinician-rated toolSuicd based cln eval2024
M1356Patients who died during the measurement periodPt died dur meas pd2024
M1357Patients who had a reduction in suicidal ideation and/or behavior upon follow-up assessment within 120 days of index assessmentPt w/red suic idea 120 days2024
M1358Patients who did not have a reduction in suicidal ideation and/or behavior upon follow-up assessment within 120 days of index assessmentPts no <suicd idea 120 dys2024
M1359Index assessment during the denominator period when the suicidal ideation and/or behavior symptoms or increased suicide risk by clinician determination occurs and a non-zero c-ssrs score is obtainedIndx suicd idea, no 0 scr2024
M1360Suicidal ideation and/or behavior symptoms based on the c-ssrsSuicd c-ssrs assessment2024
M1361Suicide risk based on their clinician's evaluation or a clinician-rated toolSuicd based cln eval2024
M1362Patients who died during the measurement periodPt died dur meas pd2024
M1363Patients who did not have a follow-up assessment within 120 days of the index assessmentPts no f/u 120 dys2024
M1364Calculated 10-year ascvd risk score of >= 20 percent during the performance periodAscvd risk >=20pct2024
M1365Patient encounter during the performance period with hospice and palliative care specialty code 17Hosp+pall care spec code 172024
M1366Focusing on women's health mips value pathwayFocus on women's health mvp2024
M1367Quality care for the treatment of ear, nose, and throat disorders mips value pathwayQual care ent disorder mvp2024
M1368Prevention and treatment of infectious disorders including hepatitis c and hiv mips value pathwayPrev trt inf d/o hiv/hep mvp2024
M1369Quality care in mental health and substance use disorders mips value pathwayQualcare mental hlth/sud mvp2024
M1370Rehabilitative support for musculoskeletal care mips value pathwayRehab support msk care mvp2024
M1371Most recent glycemic status assessment (hba1c or gmi) level < 7.0%Mst rec gsa<72025
M1372Most recent glycemic status assessment (hba1c or gmi) level >= 7.0% and < 8.0%Mst rec gsa >=7 and<82025
M1373Most recent glycemic status assessment (hba1c or gmi) level >= 8.0% and <= 9.0%Mst rec gsa >=8 and <=92025
M1374An additional encounter with an ra diagnosis during the performance period or prior performance period that is at least 90 days before or after an encounter with an ra diagnosis during the performance periodRa dx enc 90 days dur per pd2025
M1375An additional encounter with an ra diagnosis during the performance period or prior performance period that is at least 90 days before or after an encounter with an ra diagnosis during the performance periodRa dx enc 90 days dur per pd2025
M1376An additional encounter with an ra diagnosis during the performance period or prior performance period that is at least 90 days before or after an encounter with an ra diagnosis during the performance periodRa dx enc 90 days dur per pd2025
M1377Recommended follow-up interval for repeat colonoscopy of 10 years documented in colonoscopy report and communicated with patientFu colscop 10 yr doc w/ disc2025
M1378Documentation of medical reason(s) for not recommending 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, other medical reasons)Med rsn no 10 yr fu colscope2025
M1379A 10 year follow-up interval for colonoscopy not recommended, reason not otherwise specified10 yr fu no rec rsn not giv2025
M1380Filled at least two prescriptions during the performance period for any combination of the qualifying oral antipsychotic medications listed under "denominator note" or the long-acting injectable antipsychotic medications listed under "denominator note"2 rx in perf pd any com meds2025
M1381Patients with secondary stroke (e.g., a subsequent stroke that may occur with vasospasm in the setting of subarachnoid hemorrhage) within 5 days of the initial procedurePt sec strk wthin 5 days2025
M1382Patient encounter during the performance period with place of service code 11Enc dur perf pd pos 112025
M1383Acute pvdAcute pvd2025
M1384Patients who died during the performance periodPt died dur perf pd2025
M1385Documentation of patient reasons for patients who were not seen for the second pam survey (e.g., less than four months between baseline pam assessment and follow-upPt rsn not seen 2nd pam2025
M1386Patients with an excisional surgery for melanoma or melanoma in situ in the past 5 years with an initial ajcc staging of 0, i, or ii at the start of the performance periodExc sx melmn or mlnm is2025
M1387Patients who died during the performance periodPt died dur perf pd2025
M1388Patients with documentation of an exam performed for recurrence of melanomaPt doc exm rec melmn2025
M1390Patients who do not have a documented exam performed for recurrence of melanoma or no documentation within the performance periodPt no doc exm for rec2025
M1391All patients who were diagnosed with recurrent melanoma during the current performance periodAll pt dx w/ rec mlnm2025
M1392Documentation of patient reasons for no examination, i.e., refusal of examination or lost to follow-up (documentation must include information that the clinician was unable to reach the patient by phone, mail or secure electronic mail - at least one method must be documented)Pt rsn no exm or lst to fu2025
M1393Patients who were not diagnosed with recurrent melanoma during the current performance periodPr no dx rec mlnm2025
M1394Stages i-iii breast cancerStg i-iii br ca2025
M1395Patients receiving an initial chemotherapy regimen with a defined duration with the eligible clinician or groupInit chemo w/def dur ec grp2025
M1396Patients on a therapeutic clinical trialPt ther clin trial2025
M1397Patients with recurrence/disease progressionPt w/ recur/prog2025
M1398Patients with baseline and follow-up promis surveys documented in the medical recordBslne and fu promis doc2025
M1399Patients who leave the practice during the follow-up periodPt lve prac2025
M1400Patients who died during the follow-up periodPt died dur perf pd2025
M1401Stages i-iii breast cancerStg i-iii br ca2025
M1402Patients receiving an initial chemotherapy regimen with a defined duration with the eligible clinician or groupInit chemo w/def dur ec grp2025
M1403Patients with baseline and follow-up promis surveys documented in the medical recordBslne and fu promis doc2025
M1404Patients on a therapeutic clinical trialPt ther clin trial2025
M1405Patients with recurrence/disease progressionPt w/ recur/prog2025
M1406Patients who leave the practice during the follow-up periodPt lve prac2025
M1407Patients who died during the follow-up periodPt died dur perf pd2025
M1408Patients who have germline brca testing completed before diagnosis of epithelial ovarian, fallopian tube, or primary peritoneal cancerGmln brca bef dx ca2025
M1409Patients who received germline testing for brca1 and brca2 or genetic counseling completed within 6 months of diagnosisRecd gmln brca1/brca2 couns2025
M1410Patients who did not have germline testing for brca1 and brca2 or genetic counseling completed within 6 months of diagnosisNo gmln brca1/brca2 couns2025
M1411Currently on first-line immune checkpoint inhibitors without chemotherapy1st ln ici no chemo2025
M1412Patients with metastatic nsclc with epidermal growth factor receptor (egfr) mutations, alk genomic tumor aberrations, or other targetable genomic abnormalities with approved first-line targeted therapy, such as nsclc with ros1 rearrangement, braf v600e mutation, ntrk 1/2/3 gene fusion, met ex14 skipping mutation, and ret rearrangementMet nsclc w/ egfr alk oth ab2025
M1413Patients who had a positive pd-l1 biomarker expression test result prior to the initiation of first-line immune checkpoint inhibitor therapyPos pdl1 bef init ici tx2025
M1414Documentation of medical reason(s) for not performing the pd-l1 biomarker expression test prior to initiation of first-line immune checkpoint inhibitor therapy (e.g., patient is in an urgent or emergent situation where delay of treatment would jeopardize the patient's health status; other medical reasons/contraindication)Med rsn no pdl1 bef 1st ther2025
M1415Patients who did not have a positive pd-l1 biomarker expression test result prior to the initiation of first-line immune checkpoint inhibitor therapyNo pos pdl1 bef ici ther2025
M1416Patient received hospice services any time during the performance periodPt rec hosp2025
M1417Patients who are up to date on their covid-19 vaccinations as defined by cdc recommendations on current vaccinationPt up to date cov2025
M1418Patients who are not up to date on their covid-19 vaccinations as defined by cdc recommendations on current vaccination because of a medical contraindication documented by clinicianMed rsn not up to date cov2025
M1419Patients who are not up to date on their covid-19 vaccinations as defined by cdc recommendations on current vaccinationPt not up to date cov2025
M1420Complete ophthalmologic care mips value pathwayComplete ophthalmologic mvp2025
M1421Dermatological care mips value pathwayDermatological care mvp2025
M1422Gastroenterology care mips value pathwayGastroenterology care mvp2025
M1423Optimal care for patients with urologic conditions mips value pathwayOpt care urologic cnd mvp2025
M1424Pulmonology care mips value pathwayPulmonology care mvp2025
M1425Surgical care mips value pathwaySurgical care mvp2025
M1426Encounters conducted via telehealthTelehealth enc2026
M1427Documentation of medical reason(s) for performing a bone scan (including documented pain related to prostate cancer, salvage therapy, other medical reasons)Doc med rsn bone scn2026
M1428Patients who have bilateral absence of eyes any time during the patient's history through the end of the measurement periodBilateral absence of eyes2026
M1429Retinal exam finding with evidence of retinopathy in left, right or both eyes with severity level documentedRetinopathy in od, os, ou2026
M1430Retinal exam finding without evidence of retinopathy in both eyes with severity level documented (in measurement year or in the prior year)Ret exm ou no retinopthy doc2026
M1431Encounters conducted via telehealthTelehealth enc2026
M1432Encounters conducted via telehealthTelehealth enc2026
M1433Patient on oral chemotherapy on or within 30 days before denominator eligible encounterOral chemo wthn 30 days enc2026
M1434Patient on oral chemotherapy on or within 30 days after denominator eligible encounterOrl chemo wthn 30 d post enc2026
M1435Patient on oral chemotherapy during the performance periodOral chemo in perf pd2026
M1436Encounters conducted via telehealthTelehealth enc2026
M1437Encounters conducted via telehealthTelehealth enc2026
M1438Time last known well to hospital arrival less than or equal to 3.5 hours (<= 210 minutes)Lst knwn well <=210 min2026
M1439Significant ocular conditions that impact the visual outcome of surgerySig ocu cond imp surg out2026
M1440Encounters conducted via telehealthTelehealth enc2026
M1441Encounter corresponds to initial diagnosis of sleep apnea or first contact with sleep apnea diagnosed patientInit dx slp apn = 1st enc2026
M1442Encounters conducted via telehealthTelehealth enc2026
M1443Encounters conducted via telehealthTelehealth enc2026
M1444Delivery at < 39 weeks of gestationDel < 39 weeks gest2026
M1445Postpartum care visit before or at 12 weeks of giving birthPp care visit by 12 weeks2026
M1446Patients who died any time prior to the end of the measure assessment periodPt died bef end meas pd2026
M1447Patients with an active diagnosis of bipolar disorder any time prior to the end of the measure assessment periodPt dx bd bef end meas pd2026
M1448Patients with an active diagnosis of personality disorder any time prior to the end of the measure assessment periodPt dx pd bef end meas pd2026
M1449Patients with an active diagnosis of schizophrenia or psychotic disorder any time prior to the end of the measure assessment periodPt dx scz/pys bef end msr pd2026
M1450Patients who received hospice or palliative care service any time during denominator identification period or the measure assessment periodPt hos/pal care dur id/pf pd2026
M1451Patients with an active diagnosis of pervasive developmental disorder any time prior to the end of the measure assessment periodPt dx ppd dur id/pf pd2026
M1452Patient ever had a diagnosis of dementiaPt dx dementia ever2026
M1453Patients with a pre-operative visual acuity better than 20/40Preop vis acu > 20/402026
M1454New ciedNew cied2026
M1455Replaced or revised ciedRep/rev cied2026
M1456Patient had a heart transplantPt had htx2026
M1457Patient had a diagnosis of asthma with any contact during the current or prior performance period or had asthma present on an active problem list any time during the performance periodDx asth dur crnt/prv perf pd2026
M1458Patient died prior to the end of the performance periodPt died bef end meas pd2026
M1459Patient was in hospice or receiving palliative care services at any time during the performance periodPt hosp/pal care dur perf pd2026
M1460Diagnosis for chronic obstructive pulmonary disease, emphysema, cystic fibrosis, or acute respiratory failureDx copd, cf, or arf2026
M1461Patient diagnosis for chronic hepatitis cPt dx chron hepc2026
M1462Patients with clinical indications for imaging of the headPt clin ind hd image2026
M1463Documentation of at least two attempts to follow up with patient within 180 days of treatment2 f/u wthn 180 day rx atmp2026
M1464No documentation of at least two attempts to follow up with patient within 180 days of treatmentNo record of f/u by 180 days2026
M1465Patient follow up more than 180 days after treatmentF/u > 180 days after rx2026
M1466Patient had a lumbar fusion on the same date as the discectomy/laminectomy procedurePt disc/lam proc same day2026
M1467Patients with an existing diagnosis of lynch syndromePt dx lynch syn2026
M1468Patient received recommended doses of hepatitis b vaccination based on ageHep b vaccine received2026
M1469Patient has a history of hepatitis b illness or received a hepatitis b surface antigen, hepatitis b surface antibody, or total antibody to hepatitis b core antigen test with a positive result any time before or during the measurement periodHx of hep b, or pos bld test2026
M1470Documentation of medical reason(s) for not administering hepatitis b vaccine (e.g., prior anaphylaxis due to the hepatitis b vaccine)Hep b vac not rec'd med rsn2026
M1471Documentation that patient is a medicare fee-for-service beneficiary and without additional supplementary insurance coverage for whom hep b vaccination is not reimbursable under current medicare part b coverage rulesFfs hep b not covered2026
M1472Patient did not receive recommended doses of hepatitis b vaccination based on ageHep b vaccine not received2026
M1473Patient situations, at any point during the denominator identification period, where the patient's functional capacity or motivation (or lack thereof) to improve may impact the accuracy of results of validated tools, such as delirium, dementia, intellectual disabilities, and pervasive and specific development disordersPt func cap not allow impr2026
M1474Patients with diagnosis of dementiaPt dx dementia2026
M1475Patients with diagnosis of huntington's diseasePt dx huntington2026
M1476Patients with diagnosis of cognitive impairment or alzheimer's diseasePt dx cog imp or ad2026
M1477Diagnosis of deliriumDx delirium2026
M1478Psychoactive substance abusePsychoactive sub abuse2026
M1479Patients whose functional capacity or motivation (or lack thereof) to improve may impact the accuracy of results of validated tools such as delirium, dementia, intellectual disabilities, and pervasive and specific development disordersPt func cap not allow impr2026
M1480Patients whose functional capacity or motivation (or lack thereof) to improve may impact the accuracy of results of validated tools such as delirium, dementia, intellectual disabilities, and pervasive and specific development disordersPt func cap not allow impr2026
M1481Patients receiving hospice or palliative care or who died during the measurement periodPt in hosp/pal care who died2026
M1482Positive/detectable hepatitis c virus quantitative or qualitative rna test result during the denominator identification periodPos quan hep c or qual rna2026
M1483Patients who achieve sustained virological response as identified by an hcv rna test (cpt 87522) or (cpt 87521) with a negative/undetectable hcv rna result that occurred 20 weeks to 12 months after the first positive/detectable hcv rna test result within the denominator identification periodNeg quan hep c or qual rna2026
M1484Patients who did not have a repeat hcv rna labs performed for medical reasons documented by clinician (e.g., patient with limited life expectancy, delay in treatment of hcv related to treatment of hiv, hbv, hepatocellular carcinoma, decompensated cirrhosis)No rpt hcv rna perf med rsn2026
M1485Patients who did not achieve sustained virological response as identified by an hcv rna test (cpt 87522) or (cpt 87521) with a negative/undetectable hcv rna result that occurred 20 weeks to 12 months after the first positive/detectable hcv rna test result within the denominator identification periodNeg viro resp hep c/qual rna2026
M1486Patients admitted to a skilled nursing facility (snf) during the period of evaluationPt admitted to snf dur eval2026
M1487Patients in hospice in the year before or during the period of evaluationPt adm to hospice dur eval2026
M1488Patients with a diagnosis for dementia in the year before or during the period of evaluationDx dementia in msr timeframe2026
M1489Patient status documentedPt status doc2026
M1490Patient status not documentedPt status not doc2026
M1491Receiving esrd mcp dialysis services by the provider during the performance periodRec'd esrd mcp dur perf pd2026
M1492Patients who did not report a fallNo reported fall2026
M1493Documentation of falls not performed due to medical reasons (e.g., syncope, vertigo and related disorders, restless leg syndrome, tourette syndrome/tic disorder, back pain, concussion/mild traumatic brain injury (mtbi), cervical dystonia, or epilepsy)No fall doc med rsn2026
M1494Patients that reported a fall since the last visitFall rep since last visit2026
M1495Patients that reported a fall occurred who had a plan of care for falls documented or patients that did not report a fallFall w/ poc, no fall2026
M1496Patients that had a fall who did not have a plan of care for falls documented or do not have documentation of being assessed for fallsNo doc of fall or poc2026
M1497Documentation of falls not performed due to medical reasons (e.g., syncope, vertigo and related disorders, restless leg syndrome, tourette syndrome/tic disorder, back pain, concussion/mild traumatic brain injury (mtbi), cervical dystonia, or epilepsy)No doc fall med rsn2026
M1498Diagnostic radiology mips value pathwayDiagnostic radiology mvp2026
M1499Interventional radiology mips value pathwayInterventional radiology mvp2026
M1500Neuropsychology mips value pathwayNeuropsychology mvp2026
M1501Pathology mips value pathwayPathology mvp2026
M1502Podiatry mips value pathwayPodiatry mvp2026
M1503Vascular surgery mips value pathwayVascular surgery mvp2026
Advertisement