Modifier and HCPCS Changes for January 2024

The following new and deleted National Level II modifiers and Healthcare Common Procedure Coding System (HCPCS) are effective for dates of service on/after January 1, 2024.

In compliance with the Health Insurance Portability and Accountability Act (HIPAA), CMS eliminated the 3-month grace period for discontinued codes in Change Request (CR) 3093 dated February 6, 2004. Effective for dates of services on/after January 1, 2010, there is no grace period for billing discontinued HCPCS codes.

Note: The inclusion of modifiers or codes on this web page do not necessarily indicate coverage. New modifiers and HCPCS identified as Durable Medical Equipment (DME) are not included in this listing.

 

New Modifiers

There are no new modifiers being implemented.

New Codes

HCPCS DESCRIPTION
A4287 Disposable collection and storage bag for breast milk, any size, any type, each
A4457 Enema tube, with or without adapter, any type, replacement only, each
A4468 Exsufflation belt, includes all supplies and accessories
A4540 Distal transcutaneous electrical nerve stimulator, stimulates peripheral nerves of the upper arm
A4541 Monthly supplies for use of device coded at e0733
A4542 Supplies and accessories for external upper limb tremor stimulator of the peripheral nerves of the wrist
A6520 Gradient compression garment, glove, padded, for nighttime use, each
A6521 Gradient compression garment, glove, padded, for nighttime use, custom, each
A6522 Gradient compression garment, arm, padded, for nighttime use, each
A6523 Gradient compression garment, arm, padded, for nighttime use, custom, each
A6524 Gradient compression garment, lower leg and foot, padded, for nighttime use, each
A6525 Gradient compression garment, lower leg and foot, padded, for nighttime use, custom, each
A6526 Gradient compression garment, full leg and foot, padded, for nighttime use, each
A6527 Gradient compression garment, full leg and foot, padded, for nighttime use, custom, each
A6528 Gradient compression garment, bra, for nighttime use, each
A6529 Gradient compression garment, bra, for nighttime use, custom, each
A6552 Gradient compression stocking, below knee, 30-40 mmhg, each
A6553 Gradient compression stocking, below knee, 30-40 mmhg, custom, each
A6554 Gradient compression stocking, below knee, 40 mmhg or greater, each
A6555 Gradient compression stocking, below knee, 40 mmhg or greater, custom, each
A6556 Gradient compression stocking, thigh length, 18-30 mmhg, custom, each
A6557 Gradient compression stocking, thigh length, 30-40 mmhg, custom, each
A6558 Gradient compression stocking, thigh length, 40 mmhg or greater, custom, each
A6559 Gradient compression stocking, full length/chap style, 18-30 mmhg, custom, each
A6560 Gradient compression stocking, full length/chap style, 30-40 mmhg, custom, each
A6561 Gradient compression stocking, full length/chap style, 40 mmhg or greater, custom, each
A6562 Gradient compression stocking, waist length, 18-30 mmhg, custom, each
A6563 Gradient compression stocking, waist length, 30-40 mmhg, custom, each
A6564 Gradient compression stocking, waist length, 40 mmhg or greater, custom, each
A6565 Gradient compression gauntlet, custom, each
A6566 Gradient compression garment, neck/head, each
A6567 Gradient compression garment, neck/head, custom, each
A6568 Gradient compression garment, torso and shoulder, each
A6569 Gradient compression garment, torso/shoulder, custom, each
A6570 Gradient compression garment, genital region, each
A6571 Gradient compression garment, genital region, custom, each
A6572 Gradient compression garment, toe caps, each
A6573 Gradient compression garment, toe caps, custom, each
A6574 Gradient compression arm sleeve and glove combination, custom, each
A6575 Gradient  compression arm sleeve and glove combination, each
A6576 Gradient  compression arm sleeve, custom, medium weight, each
A6577 Gradient  compression arm sleeve, custom, heavy weight, each
A6578 Gradient  compression arm sleeve, each
A6579 Gradient compression glove, custom, medium weight, each
A6580 Gradient  compression glove, custom, heavy weight, each
A6581 Gradient compression glove, each
A6582 Gradient compression gauntlet, each
A6583 Gradient compression wrap with adjustable straps, below knee, 30-50 mmhg, each
A6584 Gradient compression wrap with adjustable straps, not otherwise specified
A6585 Gradient pressure wrap with adjustable straps, above knee, each
A6586 Gradient pressure wrap with adjustable straps, full leg, each
A6587 Gradient pressure wrap with adjustable straps, foot, each
A6588 Gradient pressure wrap with adjustable straps, arm, each
A6589 Gradient pressure wrap with adjustable straps, bra, each
A6593 Accessory for gradient compression garment or wrap with adjustable straps, non-otherwise specified
A6594 Gradient compression bandaging supply, bandage liner, lower extremity, any size or length, each
A6595 Gradient compression bandaging supply, bandage liner, upper extremity, any size or length, each
A6596 Gradient compression bandaging supply, conforming gauze, per linear yard, any width, each
A6597 Gradient compression bandage roll, elastic long stretch, linear yard, any width, each
A6598 Gradient compression bandage roll, elastic medium stretch, per linear yard, any width, each
A6599 Gradient compression bandage roll, inelastic short stretch, per linear yard, any width, each
A6600 Gradient compression bandaging supply, high density foam sheet, per 250 square centimeters, each
A6601 Gradient compression bandaging supply, high density foam pad, any size or shape, each
A6602 Gradient compression bandaging supply, high density foam roll for bandage, per linear yard, any width, each
A6603 Gradient compression bandaging supply, low density channel foam sheet, per 250 square centimeters, each
A6604 Gradient compression bandaging supply, low density flat foam sheet, per 250 square centimeters, each
A6605 Gradient compression bandaging supply, padded foam, per linear yard, any width, each
A6606 Gradient compression bandaging supply, padded textile, per linear yard, any width, each
A6607 Gradient compression bandaging supply, tubular protective absorption layer, per linear yard, any width, each
A6608 Gradient compression bandaging supply, tubular protective absorption padded layer, per linear yard, any width, each
A6609 Gradient compression bandaging supply, not otherwise specified
A6610 Gradient compression stocking, below knee, 18-30 mmhg, custom, each
A7023 Mechanical allergen particle barrier/inhalation filter, cream, nasal, topical
A9608 Flotufolastat f 18, diagnostic, 1 millicurie
A9609 Fludeoxyglucose f18 up to 15 millicuries
C1600 Catheter, transluminal intravascular lesion preparation device, bladed, sheathed (insertable)
C1601 Endoscope, single-use (i.e. disposable), pulmonary, imaging/illumination device (insertable)
C1602 Orthopedic/device/drug matrix/absorbable bone void filler, antimicrobial-eluting (implantable)
C1603 Retrieval device, insertable, laser (used to retrieve intravascular inferior vena cava filter)
C1604 Graft, transmural transvenous arterial bypass (implantable), with all delivery system components
C7556 Bronchoscopy, rigid or flexible, with bronchial alveolar lavage and transendoscopic endobronchial ultrasound (ebus) during bronchoscopic diagnostic or therapeutic intervention(s) for peripheral lesion(s), including fluoroscopic guidance, when performed
C7557 Catheter placement in coronary artery(s) for coronary angiography, including intraprocedural injection(s) for coronary angiography, imaging supervision and interpretation with left heart catheterization including intraprocedural injection(s) for left ventriculography, when performed and intraprocedural coronary fractional flow reserve (ffr) with 3d functional mapping of color-coded ffr values for the coronary tree, derived from coronary angiogram data, for real-time review and interpretation of possible atherosclerotic stenosis(es) intervention
C7558 Catheter placement in coronary artery(s) for coronary angiography, including intraprocedural injection(s) for coronary angiography, imaging supervision and interpretation with right and left heart catheterization including intraprocedural injection(s) for left ventriculography, when performed, catheter placement(s) in bypass graft(s) (internal mammary, free arterial, venous grafts) with bypass graft angiography with pharmacologic agent administration (eg, inhaled nitric oxide, intravenous infusion of nitroprusside, dobutamine, milrinone, or other agent) including assessing hemodynamic measurements before, during, after and repeat pharmacologic agent administration, when performed
C7560 Endoscopic retrograde cholangiopancreatography (ercp) with removal of foreign body(s) or stent(s) from biliary/pancreatic duct(s) and endoscopic cannulation of papilla with direct visualization of pancreatic/common bile duct(s)
C7561 Debridement, bone (includes epidermis, dermis, subcutaneous tissue, muscle and/or fascia, if performed); first 20 sq cm or less with manual preparation and insertion of drug-delivery device(s), deep (e.g., subfascial)
C7903 Group psychotherapy service for diagnosis, evaluation, or treatment of a mental health or substance use disorder provided remotely by hospital staff who are licensed to provide mental health services under applicable state law(s), when the patient is in their home, and there is no associated professional service
C9159 Injection, prothrombin complex concentrate (human), balfaxar, per i.u. of factor ix activity
C9160 Injection, daxibotulinumtoxina-lanm, 1 unit
C9161 Injection, aflibercept hd, 1 mg
C9162 Injection, avacincaptad pegol, 0.1 mg
C9163 Injection, talquetamab-tgvs, 0.25 mg
C9164 Cantharidin for topical administration, 0.7%, single unit dose applicator (3.2 mg)
C9165 Injection, elranatamab-bcmm, 1 mg
C9793 3d predictive model generation for pre-planning of a cardiac procedure, using data from cardiac computed tomographic angiography with report
C9794 Therapeutic radiology simulation-aided field setting; complex, including acquisition of pet and ct imaging data required for radiopharmaceutical-directed radiation therapy treatment planning (i.e., modeling)
C9795 Stereotactic body radiation therapy, treatment delivery, per fraction to 1 or more lesions, including image guidance and real-time positron emissions-based delivery adjustments to 1 or more lesions, entire course not to exceed 5 fractions
D0396 3d printing of a 3d dental surface scan
D1301 Immunization counseling
D2976 Band stabilization - per tooth
D2989 Excavation of a tooth resulting in the determination of non-restorability
D2991 Application of hydroxyapatite regeneration medicament - per tooth
D6089 Accessing and retorquing loose implant screw - per screw
D7284 Excisional biopsy of minor salivary glands
D7939 Indexing for osteotomy using dynamic robotic assisted or dynamic navigation
D9938 Fabrication of a custom removable clear plastic temporary aesthetic appliance
D9939 Placement of a custom removable clear plastic temporary aesthetic appliance
D9954 Fabrication and delivery of oral appliance therapy (oat) morning repositioning device
D9955 Oral appliance therapy (oat) titration visit
D9956 Administration of home sleep apnea test
D9957 Screening for sleep related breathing disorders
E0492 Power source and control electronics unit for oral device/appliance for neuromuscular electrical stimulation of the tongue muscle, controlled by phone application
E0493 Oral device/appliance for neuromuscular electrical stimulation of the tongue muscle, used in conjunction with the power source and control electronics unit, controlled by phone application, 90-day supply
E0530 Electronic positional obstructive sleep apnea treatment, with sensor, includes all components and accessories, any type
E0678 Non-pneumatic sequential compression garment, full leg
E0679 Non-pneumatic sequential compression garment, half leg
E0680 Non-pneumatic compression controller with sequential calibrated gradient pressure
E0681 Non-pneumatic compression controller without calibrated gradient pressure
E0682 Non-pneumatic sequential compression garment, full arm
E0732 Cranial electrotherapy stimulation (ces) system, any type
E0733 Transcutaneous electrical nerve stimulator for electrical stimulation of the trigeminal nerve
E0734 External upper limb tremor stimulator of the peripheral nerves of the wrist
E0735 Non-invasive vagus nerve stimulator
E1301 Whirlpool tub, walk-in, portable
E2001 Suction pump, home model, portable or stationary, electric, any type, for use with external urine management system
E3000 Speech volume modulation system, any type, including all components and accessories
G0011 Individual counseling for pre-exposure prophylaxis (prep) by physician or qualified health care professional (qhp )to prevent human immunodeficiency virus (hiv), includes hiv risk assessment (initial or continued assessment of risk), hiv risk reduction and medication adherence, 15-30 minutes
G0012 Injection of pre-exposure prophylaxis (prep) drug for hiv prevention, under skin or into muscle
G0013 Individual counseling for pre-exposure prophylaxis (prep) by clinical staff to prevent human immunodeficiency virus (hiv), includes: hiv risk assessment (initial or continued assessment of risk), hiv risk reduction and medication adherence
G0017 Psychotherapy for crisis furnished in an applicable site of service (any place of service at which the non-facility rate for psychotherapy for crisis services applies, other than the office setting); first 60 minutes
G0018 Psychotherapy for crisis furnished in an applicable site of service (any place of service at which the non-facility rate for psychotherapy for crisis services applies, other than the office setting); each additional 30 minutes (list separately in addition to code for primary service)
G0019 Community health integration services performed by certified or trained auxiliary personnel, including a community health worker, under the direction of a physician or other practitioner; 60 minutes per calendar month, in the following activities to address social determinants of health (sdoh) need(s) that are significantly limiting the ability to diagnose or treat problem(s) addressed in an initiating visit: person-centered assessment, performed to better understand the individualized context of the intersection between the sdoh need(s) and the problem(s) addressed in the initiating visit. ++ conducting a person-centered assessment to understand patient's life story, strengths, needs, goals, preferences and desired outcomes, including understanding cultural and linguistic factors and including unmet sdoh needs (that are not separately billed). ++ facilitating patient-driven goal-setting and establishing an action plan. ++ providing tailored support to the patient as needed to accomplish the practitioner's treatment plan. practitioner, home-, and community-based care coordination. ++ coordinating receipt of needed services from healthcare practitioners, providers, and facilities; and from home- and community-based service providers, social service providers, and caregiver (if applicable). ++ communication with practitioners, home- and community-based service providers, hospitals, and skilled nursing facilities (or other health care facilities) regarding the patient's psychosocial strengths and needs, functional deficits, goals, preferences, and desired outcomes, including cultural and linguistic factors. ++ coordination of care transitions between and among health care practitioners and settings, including transitions involving referral to other clinicians; follow-up after an emergency department visit; or follow-up after discharges from hospitals, skilled nursing facilities or other health care facilities. ++ facilitating access to community-based social services (e.g., housing, utilities, transportation, food assistance) to address the sdoh need(s). health education- helping the patient contextualize health education provided by the patient's treatment team with the patient's individual needs, goals, and preferences, in the context of the sdoh need(s), and educating the patient on how to best participate in medical decision-making. building patient self-advocacy skills, so that the patient can interact with members of the health care team and related community-based services addressing the sdoh need(s), in ways that are more likely to promote personalized and effective diagnosis or treatment. health care access / health system navigation. ++ helping the patient access healthcare, including identifying appropriate practitioners or providers for clinical care and helping secure appointments with them. facilitating behavioral change as necessary for meeting diagnosis and treatment goals, including promoting patient motivation to participate in care and reach person-centered diagnosis or treatment goals. facilitating and providing social and emotional support to help the patient cope with the problem(s) addressed in the initiating visit, the sdoh need(s), and adjust daily routines to better meet diagnosis and treatment goals. leveraging lived experience when applicable to provide support, mentorship, or inspiration to meet treatment goals
G0022 Community health integration services, each additional 30 minutes per calendar month (list separately in addition to g0019)
G0023 Principal illness navigation services by certified or trained auxiliary personnel under the direction of a physician or other practitioner, including a patient navigator; 60 minutes per calendar month, in the following activities:  person-centered assessment, performed to better understand the individual context of the serious, high-risk condition. ++ conducting a person-centered assessment to understand the patient's life story, strengths, needs, goals, preferences, and desired outcomes, including understanding cultural and linguistic factors and including unmet sdoh needs (that are not separately billed). ++ facilitating patient-driven goal setting and establishing an action plan. ++ providing tailored support as needed to accomplish the practitioner's treatment plan.  identifying or referring patient (and caregiver or family, if applicable) to appropriate supportive services.  practitioner, home, and community-based care coordination. ++ coordinating receipt of needed services from healthcare practitioners, providers, and facilities; home- and community-based service providers; and caregiver (if applicable). ++ communication with practitioners, home-, and community-based service providers, hospitals, and skilled nursing facilities (or other health care facilities) regarding the patient's psychosocial strengths and needs, functional deficits, goals, preferences, and desired outcomes, including cultural and linguistic factors. ++ coordination of care transitions between and among health care practitioners and settings, including transitions involving referral to other clinicians; follow-up after an emergency department visit; or follow-up after discharges from hospitals, skilled nursing facilities or other health care facilities. ++ facilitating access to community-based social services (e.g., housing, utilities, transportation, likely to promote personalized and effective treatment of their condition.  health care access / health system navigation. ++ helping the patient access healthcare, including identifying appropriate practitioners or providers for clinical care,  and helping secure appointments with them. ++ providing the patient with information/resources to consider participation in clinical trials or clinical research as applicable.  facilitating behavioral change as necessary for meeting diagnosis and treatment goals, including promoting patient motivation to participate in care and reach person-centered diagnosis or treatment goals.  facilitating and providing social and emotional support to help the patient cope with the condition, sdoh need(s), and adjust daily routines to better meet diagnosis and treatment goals.  leverage knowledge of the serious, high-risk condition and/or lived experience when applicable to provide support, mentorship, or inspiration to meet treatment goals
G0024 Principal illness navigation services, additional 30 minutes per calendar month (list separately in addition to g0023)
G0136 Administration of a standardized, evidence-based social determinants of health risk assessment tool, 5-15 minutes
G0137 Intensive outpatient services; weekly bundle, minimum of 9 services over a 7 contiguous day period, which can include individual and group therapy with physicians or psychologists (or other mental health professionals to the extent authorized under state law); occupational therapy requiring the skills of a qualified occupational therapist; services of social workers, trained psychiatric nurses, and other staff trained to work with psychiatric patients; individualized activity therapies that are not primarily recreational or diversionary; family counseling (the primary purpose of which is treatment of the individual's condition); patient training and education (to the extent that training and educational activities are closely and clearly related to individual's care and treatment); diagnostic services; and such other items and services (excluding meals and transportation) that are reasonable and necessary for the diagnosis or active treatment of the individual's condition, reasonably expected to improve or maintain the individual's condition and functional level and to prevent relapse or hospitalization, and furnished pursuant to such guidelines relating to frequency and duration of services in accordance with a physician certification and plan of treatment (provision of the services by a medicare-enrolled opioid treatment program); list separately in addition to code for primary procedure
G0140 Principal illness navigation - peer support by certified or trained auxiliary personnel under the direction of a physician or other practitioner, including a certified peer specialist; 60 minutes per calendar month, in the following activities:  person-centered interview, performed to better understand the individual context of the serious, high-risk condition. ++ conducting a person-centered interview to understand the patient's life story, strengths, needs, goals, preferences, and desired outcomes, including understanding cultural and linguistic factors, and including unmet sdoh needs (that are not billed separately). ++ facilitating patient-driven goal setting and establishing an action plan. ++ providing tailored support as needed to accomplish the person-centered goals in the practitioner's treatment plan. identifying or referring patient (and caregiver or family, if applicable) to appropriate supportive services. practitioner, home, and community-based care communication. ++ assist the patient in communicating with their practitioners, home-, and community-based service providers, hospitals, and skilled nursing facilities (or other health care facilities) regarding the patient's psychosocial strengths and needs, goals, preferences, and desired outcomes, including cultural and linguistic factors. ++ facilitating access to community-based social services (e.g., housing, utilities, transportation, food assistance) as needed to address sdoh need(s). health education. helping the patient contextualize health education provided by the patient's treatment team with the patient's individual needs, goals, preferences, and sdoh need(s), and educating the patient (and caregiver if applicable) on how to best participate in medical decision-making. building patient self-advocacy skills, so that the patient can interact with members of the health care team and related community-based services (as needed), in ways that are more likely to promote personalized and effective treatment of their condition. developing and proposing strategies to help meet person-centered treatment goals and supporting the patient in using chosen strategies to reach person-centered treatment goals. facilitating and providing social and emotional support to help the patient cope with the condition, sdoh need(s), and adjust daily routines to better meet person-centered diagnosis and treatment goals. leverage knowledge of the serious, high-risk condition and/or lived experience when applicable to provide support, mentorship, or inspiration to meet treatment goals
G0146 Principal illness navigation - peer support, additional 30 minutes per calendar month (list separately in addition to g0140)
G9886 Behavioral counseling for diabetes prevention, in-person, group, 60 minutes
G9887 Behavioral counseling for diabetes prevention, distance learning, 60 minutes
G9888 Maintenance 5% wl from baseline weight in months 7-12
J0184 Injection, amisulpride, 1 mg
J0217 Injection, velmanase alfa-tycv, 1 mg
J0391 Injection, artesunate, 1 mg
J0402 Injection, aripiprazole (abilify asimtufii), 1 mg
J0576 Injection, buprenorphine extended-release (brixadi), 1 mg
J0688 Injection, cefazolin sodium (hikma), not therapeutically equivalent to j0690, 500 mg
J0750 Emtricitabine 200mg and tenofovir disoproxil fumarate 300mg, oral, fda approved prescription, only for use as hiv pre-exposure prophylaxis (not for use as treatment of hiv)
J0751 Emtricitabine 200mg and tenofovir alafenamide 25mg, oral, fda approved prescription, only for use as hiv pre-exposure prophylaxis (not for use as treatment of hiv)
J0799 Fda approved prescription drug, only for use as hiv pre-exposure prophylaxis (not for use as treatment of hiv), not otherwise classified
J0873 Injection, daptomycin (xellia) not therapeutically equivalent to j0878, 1 mg
J1105 Dexmedetomidine, oral, 1 mcg
J1304 Injection, tofersen, 1 mg
J1412 Injection, valoctocogene roxaparvovec-rvox, per ml, containing nominal 2 x 10^13 vector genomes
J1413 Injection, delandistrogene moxeparvovec-rokl, per therapeutic dose
J1596 Injection, glycopyrrolate, 0.1 mg
J1939 Injection, bumetanide, 0.5 mg
J2404 Injection, nicardipine, 0.1 mg
J2508 Injection, pegunigalsidase alfa-iwxj, 1 mg
J2679 Injection, fluphenazine hcl, 1.25 mg
J2799 Injection, risperidone (uzedy), 1 mg
J3401 Beremagene geperpavec-svdt for topical administration, containing nominal 5 x 10^9 pfu/ml vector genomes, per 0.1 ml
J3425 Injection, hydroxocobalamin, 10 mcg
J9052 Injection, carmustine (accord), not therapeutically equivalent to j9050, 100 mg
J9072 Injection, cyclophosphamide, (dr. reddy's), 5 mg
J9172 Injection, docetaxel (ingenus) not therapeutically equivalent to j9171, 1 mg
J9255 Injection, methotrexate (accord) not therapeutically equivalent to j9250 and j9260, 50 mg
J9258 Injection, paclitaxel protein-bound particles (teva) not therapeutically equivalent to j9264, 1 mg
J9286 Injection, glofitamab-gxbm, 2.5 mg
J9321 Injection, epcoritamab-bysp, 0.16 mg
J9324 Injection, pemetrexed (pemrydi rtu), 10 mg
J9333 Injection, rozanolixizumab-noli, 1 mg
J9334 Injection, efgartigimod alfa, 2 mg and hyaluronidase-qvfc
L3161 Foot, adductus positioning device, adjustable
L5615 Addition, endoskeletal knee-shin system, 4 bar linkage or multiaxial, fluid swing and stance phase control
L5926 Addition to lower extremity prosthesis, endoskeletal, knee disarticulation, above knee, hip disarticulation, positional rotation unit, any type
M1211 Most recent hemoglobin a1c level > 9.0%
M1212 Hemoglobin a1c level is missing, or was not performed during the measurement period (12 months)
M1213 No history of spirometry results with confirmed airflow obstruction (fev1/fvc < 70%) and present spirometry is >= 70%
M1214 Spirometry results with confirmed airflow obstruction (fev1/fvc < 70%) documented and reviewed
M1215 Documentation of medical reason(s) for not documenting and reviewing spirometry results (e.g., patients with dementia or tracheostomy)
M1216 No spirometry results with confirmed airflow obstruction (fev1/fvc < 70%) documented and/or no spirometry performed with results documented during the encounter
M1217 Documentation of system reason(s) for not documenting and reviewing spirometry results (e.g., spirometry equipment not available at the time of the encounter)
M1218 Patient has copd symptoms (e.g., dyspnea, cough/sputum, wheezing)
M1219 Anaphylaxis due to the vaccine on or before the date of the encounter
M1220 Dilated retinal eye exam with interpretation by an ophthalmologist or optometrist or artificial intelligence (ai) interpretation documented and reviewed; with evidence of retinopathy
M1221 Dilated retinal eye exam with interpretation by an ophthalmologist or optometrist or artificial intelligence (ai) interpretation documented and reviewed; without evidence of retinopathy
M1222 Glaucoma plan of care not documented, reason not otherwise specified
M1223 Glaucoma plan of care documented
M1224 Intraocular pressure (iop) reduced by a value less than 20% from the pre-intervention level
M1225 Intraocular pressure (iop) reduced by a value of greater than or equal to 20% from the pre-intervention level
M1226 Iop measurement not documented, reason not otherwise specified
M1227 Evidence-based therapy was prescribed
M1228 Patient, 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 test
M1229 Patient, 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 infection
M1230 Patient 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 given
M1231 Patient receives hcv antibody test with nonreactive result
M1232 Patient receives hcv antibody test with reactive result
M1233 Patient does not receive hcv antibody test or patient does receive hcv antibody test but results not documented, reason not given
M1234 Patient has a reactive hcv antibody test, and has a follow up hcv viral test that does not detect hcv viremia
M1235 Documentation or patient report of hcv antibody test or hcv rna test which occurred prior to the performance period
M1236 Baseline mrs > 2
M1237 Patient reason for not screening for food insecurity, housing instability, transportation needs, utility difficulties, and interpersonal safety (e.g., patient declined or other patient reasons)
M1238 Documentation 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)
M1239 Patient did not respond to the question of patient felt heard and understood by this provider and team
M1240 Patient did not respond to the question of patient felt this provider and team put my best interests first when making recommendations about my care
M1241 Patient did not respond to the question of patient felt this provider and team saw me as a person, not just someone with a medical problem
M1242 Patient did not respond to the question of patient felt this provider and team understood what is important to me in my life
M1243 Patient provided a response other than "completely true" for the question of patient felt heard and understood by this provider and team
M1244 Patient 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 care
M1245 Patient 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 problem
M1246 Patient 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 life
M1247 Patient responded "completely true" for the question of patient felt this provider and team put my best interests first when making recommendations about my care
M1248 Patient responded "completely true" for the question of patient felt this provider and team saw me as a person, not just someone with a medical problem
M1249 Patient responded "completely true" for the question of patient felt this provider and team understood what is important to me in my life
M1250 Patient responded as "completely true" for the question of patient felt heard and understood by this provider and team
M1251 Patients for whom a proxy completed the entire hu survey on their behalf for any reason (no patient involvement)
M1252 Patients 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 visit
M1253 Patients 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)
M1254 Patients who were deceased when the hu survey reached them
M1255 Patients 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)
M1256 Prior history of known cvd
M1257 Cvd risk assessment not performed or incomplete (e.g., cvd risk assessment was not documented), reason not otherwise specified
M1258 Cvd risk assessment performed, have a documented calculated risk score
M1259 Patients listed on the kidney-pancreas transplant waitlist or who received a living donor transplant within the first year following initiation of dialysis
M1260 Patients who were not listed on the kidney-pancreas transplant waitlist or patients who did not receive a living donor transplant within the first year following initiation of dialysis
M1261 Patients that were on the kidney or kidney-pancreas waitlist prior to initiation of dialysis
M1262 Patients who had a transplant prior to initiation of dialysis
M1263 Patients in hospice on their initiation of dialysis date or during the month of evaluation
M1264 Patients age 75 or older on their initiation of dialysis date
M1265 Cms medical evidence form 2728 for dialysis patients: initial form completed
M1266 Patients admitted to a skilled nursing facility (snf)
M1267 Patients not on any kidney or kidney-pancreas transplant waitlist or is not in active status on any kidney or kidney-pancreas transplant waitlist as of the last day of each month during the measurement period
M1268 Patients on active status on any kidney or kidney-pancreas transplant waitlist as of the last day of each month during the measurement period
M1269 Receiving esrd mcp dialysis services by the provider on the last day of the reporting month
M1270 Patients not on any kidney or kidney-pancreas transplant waitlist as of the last day of each month during the measurement period
M1271 Patients with dementia at any time prior to or during the month
M1272 Patients on any kidney or kidney-pancreas transplant waitlist as of the last day of each month during the measurement period
M1273 Patients who were admitted to a skilled nursing facility (snf) within one year of dialysis initiation according to the cms-2728 form
M1274 Patients who were admitted to a skilled nursing facility (snf) during the month of evaluation were excluded from that month
M1275 Patients determined to be in hospice were excluded from month of evaluation and the remainder of reporting period
M1276 Bmi documented outside normal parameters, no follow-up plan documented, no reason given
M1277 Colorectal cancer screening results documented and reviewed
M1278 Elevated or hypertensive blood pressure reading documented, and the indicated follow-up is documented
M1279 Elevated or hypertensive blood pressure reading documented, indicated follow-up not documented, reason not given
M1280 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
M1281 Blood pressure reading not documented, reason not given
M1282 Patient screened for tobacco use and identified as a tobacco non-user
M1283 Patient screened for tobacco use and identified as a tobacco user
M1284 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 consecutive days during the measurement period
M1285 Screening, diagnostic, film, digital or digital breast tomosynthesis (3d) mammography results were not documented and reviewed, reason not otherwise specified
M1286 Bmi is documented as being outside of normal parameters, follow-up plan is not completed for documented medical reason
M1287 Bmi is documented below normal parameters and a follow-up plan is documented
M1288 Documented reason for not screening or recommending a follow-up for high blood pressure
M1289 Patient 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)
M1290 Patient not eligible due to active diagnosis of hypertension
M1291 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
M1292 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
M1293 Bmi is documented above normal parameters and a follow-up plan is documented
M1294 Normal blood pressure reading documented, follow-up not required
M1295 Patients with a diagnosis or past history of total colectomy or colorectal cancer
M1296 Bmi is documented within normal parameters and no follow-up plan is required
M1297 Bmi not documented due to medical reason or patient refusal of height or weight measurement
M1298 Documentation of patient pregnancy anytime during the measurement period prior to and including the current encounter
M1299 Influenza immunization administered or previously received
M1300 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)
M1301 Patient 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)
M1302 Screening, diagnostic, film digital or digital breast tomosynthesis (3d) mammography results documented and reviewed
M1303 Hospice services provided to patient any time during the measurement period
M1304 Patient did not receive any pneumococcal conjugate or polysaccharide vaccine on or after their 19th birthday and before the end of the measurement period
M1305 Patient received any pneumococcal conjugate or polysaccharide vaccine on or after their 19th birthday and before the end of the measurement period
M1306 Patient had anaphylaxis due to the pneumococcal vaccine any time during or before the measurement period
M1307 Documentation stating the patient has received or is currently receiving palliative or hospice care
M1308 Influenza immunization was not administered, reason not given
M1309 Palliative care services provided to patient any time during the measurement period
M1310 Patient 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 user
M1311 Anaphylaxis due to the vaccine on or before the date of the encounter
M1312 Patient not screened for tobacco use
M1313 Tobacco screening not performed or tobacco cessation intervention not provided during the measurement period or in the six months prior to the measurement period
M1314 Bmi not documented and no reason is given
M1315 Colorectal cancer screening results were not documented and reviewed; reason not otherwise specified
M1316 Current tobacco non-user
M1317 Patients who are counseled on connection with a csp and explicitly opt out
M1318 Patients 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 csp
M1319 Patients who had documented contact with a csp for at least one of their screened positive hrsns within 60 days after screening
M1320 Patients who screened positive for at least 1 of the 5 hrsns
M1321 Patients 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 hg
M1322 Patients 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 eye
M1323 Patients 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 documented
M1324 Patients who had an intravitreal or periocular corticosteroid injection (e.g., triamcinolone, preservative-free triamcinolone, dexamethasone, dexamethasone intravitreal implant, or fluocinolone intravitreal implant)
M1325 Patients 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)
M1326 Patients with a diagnosis of hypotony
M1327 Patients who were not appropriately evaluated during the initial exam and/or who were not re-evaluated within 8 weeks
M1328 Patients with a diagnosis of acute vitreous hemorrhage
M1329 Patients 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 encounter
M1330 Documentation of patient reason(s) for not having a follow up exam (e.g., inadequate time for follow up)
M1331 Patients who were appropriately evaluated during the initial exam and were re-evaluated no later than 8 weeks from initial exam
M1332 Patients who were not appropriately evaluated during the initial exam and/or who were not re-evaluated within 2 weeks
M1333 Acute vitreous hemorrhage
M1334 Patients 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 encounter
M1335 Documentation of patient reason(s) for not having a follow up exam (e.g., inadequate time for follow up)
M1336 Patients who were appropriately evaluated during the initial exam and were re-evaluated no later than 2 weeks
M1337 Acute pvd
M1338 Patients 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 period
M1339 Patients 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 period
M1340 Index assessment completed using the 12-item whodas 2.0 or sds during the denominator identification period
M1341 Patients 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 period
M1342 Patients who died during the performance period
M1343 Patients who are at pam level 4 at baseline or patients who are flagged with extreme straight line response sets on the pam
M1344 Patients who did not have a baseline pam score and/or a second score within 6 to 12 month of baseline pam score
M1345 Patients who had a baseline pam score and a second score within 6 to 12 month of baseline pam score
M1346 Patients who did not have a net increase in pam score of at least 6 points within a 6 to 12 month period
M1347 Patients who achieved a net increase in pam score of at least 3 points in a 6 to 12 month period (passing)
M1348 Patients who achieved a net increase in pam score of at least 6-points in a 6 to 12 month period (excellent)
M1349 Patients who did not have a net increase in pam score of at least 3 points within 6 to 12 month period
M1350 Patients 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 encounter
M1351 Patients 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 initiation
M1352 Suicidal ideation and/or behavior symptoms based on the c-ssrs or equivalent assessment
M1353 Patients 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 encounter
M1354 Patients 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 initiation
M1355 Suicide risk based on their clinician's evaluation or a clinician-rated tool
M1356 Patients who died during the measurement period
M1357 Patients who had a reduction in suicidal ideation and/or behavior upon follow-up assessment within 120 days of index assessment
M1358 Patients who did not have a reduction in suicidal ideation and/or behavior upon follow-up assessment within 120 days of index assessment
M1359 Index 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 obtained
M1360 Suicidal ideation and/or behavior symptoms based on the c-ssrs
M1361 Suicide risk based on their clinician's evaluation or a clinician-rated tool
M1362 Patients who died during the measurement period
M1363 Patients who did not have a follow-up assessment within 120 days of the index assessment
M1364 Calculated 10-year ascvd risk score of  >= 20 percent during the performance period
M1365 Patient encounter during the performance period with hospice and palliative care specialty code 17
M1366 Focusing on women's health mips value pathway
M1367 Quality care for the treatment of ear, nose, and throat disorders mips value pathway
M1368 Prevention and treatment of infectious disorders including hepatitis c and hiv mips value pathway
M1369 Quality care in mental health and substance use disorders mips value pathway
M1370 Rehabilitative support for musculoskeletal care mips value pathway
Q0516 Pharmacy supplying fee for hiv pre-exposure prophylaxis fda approved prescription drug, per 30-days
Q0517 Pharmacy supplying fee for hiv pre-exposure prophylaxis fda approved prescription drug, per 60-days
Q0518 Pharmacy supplying fee for hiv pre-exposure prophylaxis fda approved prescription drug, per 90-days
Q4279 Vendaje ac, per square centimeter
Q4287 Dermabind dl, per square centimeter
Q4288 Dermabind ch, per square centimeter
Q4289 Revoshield + amniotic barrier, per square centimeter
Q4290 Membrane wrap-hydro, per square centimeter
Q4291 Lamellas xt, per square centimeter
Q4292 Lamellas, per square centimeter
Q4293 Acesso dl, per square centimeter
Q4294 Amnio quad-core, per square centimeter
Q4295 Amnio tri-core amniotic, per square centimeter
Q4296 Rebound matrix, per square centimeter
Q4297 Emerge matrix, per square centimeter
Q4298 Amnicore pro, per square centimeter
Q4299 Amnicore pro+, per square centimeter
Q4300 Acesso tl, per square centimeter
Q4301 Activate matrix, per square centimeter
Q4302 Complete aca, per square centimeter
Q4303 Complete aa, per square centimeter
Q4304 Grafix plus, per square centimeter
Q5132 Injection, adalimumab-afzb (abrilada), biosimilar, 10 mg

Deleted Codes

HCPCS DESCRIPTION
C9152 Injection, aripiprazole, (abilify asimtufii), 1 mg
C9153 Injection, amisulpride, 1 mg
C9154 Injection, buprenorphine extended-release (brixadi), 1 mg
C9155 Injection, epcoritamab-bysp, 0.16 mg
C9156 Flotufolastat f 18, diagnostic, 1 millicurie
C9157 Injection, tofersen, 1 mg
C9158 Injection, risperidone, (uzedy), 1 mg
C9770 Vitrectomy, mechanical, pars plana approach, with subretinal injection of pharmacologic/biologic agent
C9771 Nasal/sinus endoscopy, cryoablation nasal tissue(s) and/or nerve(s), unilateral or bilateral
C9788 Opto-acoustic imaging, breast (including axilla when performed), unilateral, with image documentation, analysis and report, obtained with ultrasound examination
C9803 Hospital outpatient clinic visit specimen collection for severe acute respiratory syndrome coronavirus  2 (sars-cov-2) (coronavirus disease [covid-19]), any specimen source
G0056 Optimizing chronic disease management mips value pathways
G2066 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
G2108 Patient 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 period
G2109 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
G2110 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
G8506 Patient receiving angiotensin converting enzyme (ace) inhibitor or angiotensin receptor blocker (arb) therapy
G8818 Patient discharge to home no later than post-operative day #7
G8825 Patient not discharged to home by post-operative day #7
G8852 Positive airway pressure therapy was prescribed
G8883 Biopsy results reviewed, communicated, tracked and documented
G8884 Clinician documented reason that patient's biopsy results were not reviewed
G8885 Biopsy results not reviewed, communicated, tracked or documented
G8941 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
G8963 Cardiac stress imaging performed primarily for monitoring of asymptomatic patient who had pci within 2 years
G8964 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)
G9192 Documentation of system reason(s) for not prescribing beta-blocker therapy (eg, other reasons attributable to the health care system)
G9229 Chlamydia, gonorrhea, and syphilis screening results not documented (patient refusal is the only allowed exception)
G9451 Patient received one-time screening for hcv infection
G9453 Documentation of patient reason(s) for not receiving one-time screening for hcv infection (e.g., patient declined, other patient reasons)
G9454 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
G9596 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
G9612 Photodocumentation of two or more cecal landmarks to establish a complete examination
G9613 Documentation of post-surgical anatomy (e.g., right hemicolectomy, ileocecal resection, etc.)
G9614 Photodocumentation of less than two cecal landmarks (i.e., no cecal landmarks or only one cecal landmark) to establish a complete examination
G9697 Documentation of patient reason(s) for not prescribing a long-acting inhaled bronchodilator
G9715 Patients who use hospice services any time during the measurement period
G9725 Patients who use hospice services any time during the measurement period
G9852 Patients who died from cancer
G9853 Patient admitted to the icu in the last 30 days of life
G9854 Patient was not admitted to the icu in the last 30 days of life
G9927 Documentation of system reason(s) for not prescribing an fda-approved anticoagulation due to patient being currently enrolled in a clinical trial related to af/atrial flutter treatment
G9995 Patients who use palliative care services any time during the measurement period
J9160 Injection, denileukin diftitox, 300 micrograms
K1001 Electronic positional obstructive sleep apnea treatment, with sensor, includes all components and accessories, any type
K1002 Cranial electrotherapy stimulation (ces) system, any type
K1003 Whirlpool tub, walk-in, portable
K1005 Disposable collection and storage bag for breast milk, any size, any type, each
K1006 Suction pump, home model, portable or stationary, electric, any type, for use with external urine management system
K1009 Speech volume modulation system, any type, including all components and accessories
K1013 Enema tube, with or without adapter, any type, replacement only, each
K1014 Addition, endoskeletal knee-shin system, 4 bar linkage or multiaxial, fluid swing and stance phase control
K1015 Foot, adductus positioning device, adjustable
K1016 Transcutaneous electrical nerve stimulator for electrical stimulation of the trigeminal nerve
K1017 Monthly supplies for use of device coded at k1016
K1018 External upper limb tremor stimulator of the peripheral nerves of the wrist
K1019 Supplies and accessories for external upper limb tremor stimulator of the peripheral nerves of the wrist
K1020 Non-invasive vagus nerve stimulator
K1021 Exsufflation belt, includes all supplies and accessories
K1022 Addition to lower extremity prosthesis, endoskeletal, knee disarticulation, above knee, hip disarticulation, positional rotation unit, any type
K1023 Distal transcutaneous electrical nerve stimulator, stimulates peripheral nerves of the upper arm
K1024 Non-pneumatic compression controller with sequential calibrated gradient pressure
K1026 Mechanical allergen particle barrier/inhalation filter, cream, nasal, topical
K1028 Power source and control electronics unit for oral device/appliance for neuromuscular electrical stimulation of the tongue muscle, controlled by phone application
K1029 Oral device/appliance for neuromuscular electrical stimulation of the tongue muscle, used in conjunction with the power source and control electronics unit, controlled by phone application, 90-day supply
K1031 Non-pneumatic compression controller without calibrated gradient pressure
K1032 Non-pneumatic sequential compression garment, full leg
K1033 Non-pneumatic sequential compression garment, half leg
M1156 Patient received active chemotherapy any time during the measurement period
M1157 Patient received bone marrow transplant any time during the measurement period
M1158 Patient had history of immunocompromising conditions prior to or during the measurement period
S0166 Injection, olanzapine, 2.5 mg
S0171 Injection, bumetanide, 0.5 mg

Source

  • Transmittal 12198, CR 13296 dated August 10, 2023
Last Updated Sep 16 , 2024