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Measure: CMS144

Heart Failure (HF): Beta-Blocker Therapy for Left Ventricular Systolic Dysfunction (LVSD)

Measure Versions

eMeasure Code Measure Year Full Version Number Title
CMS144v12 2024 12.0.000 Heart Failure (HF): Beta-Blocker Therapy for Left Ventricular Systolic Dysfunction (LVSD)
CMS144v11 2023 11 Heart Failure (HF): Beta-Blocker Therapy for Left Ventricular Systolic Dysfunction (LVSD)
CMS144v10 2022 10.0.000 Heart Failure (HF): Beta-Blocker Therapy for Left Ventricular Systolic Dysfunction (LVSD)
CMS144v9 2021 9.2.000 Heart Failure (HF): Beta-Blocker Therapy for Left Ventricular Systolic Dysfunction (LVSD)
CMS144v8 2020 8.1.000 Heart Failure (HF): Beta-Blocker Therapy for Left Ventricular Systolic Dysfunction (LVSD)
CMS144v7 2019 7.1.000 Heart Failure (HF): Beta-Blocker Therapy for Left Ventricular Systolic Dysfunction (LVSD)
CMS144v6 2018 6.0.000 Heart Failure (HF): Beta-Blocker Therapy for Left Ventricular Systolic Dysfunction (LVSD)
CMS144v5 2017 5.2.000 Heart Failure (HF): Beta-Blocker Therapy for Left Ventricular Systolic Dysfunction (LVSD)

Description

Percentage of patients aged 18 years and older with a diagnosis of heart failure (HF) with a current or prior left ventricular ejection fraction (LVEF) <= 40% who were prescribed or already taking beta-blocker therapy during the measurement period

Guidance

This eCQM is to be reported as patient-based. To satisfy this measure, it must be reported for all heart failure patients at least once during the measurement period. A range value should satisfy the logic requirement for 'Ejection Fraction' as long as the ranged observation value clearly meets the less than or equal to 40% threshold noted in the denominator logic. A range that is greater than 40% would not meet the measure requirement. In order for the Ejection Fraction result pathway to be recognized as below 40%, the result must be reported as a number with unit of %. A text string of "below 40%" or "ejection fraction between 35 and 40%" will not be recognized through electronic data capture. Although, this criteria can also be met using the Diagnosis pathway if specified as "Moderate or Severe." Beta-blocker therapy: -For patients with prior LVEF <= 40%, beta-blocker therapy should include bisoprolol, carvedilol, or sustained release metoprolol succinate. The requirement of two or more visits is to establish that the eligible professional or eligible clinician has an existing relationship with the patient. This version of the eCQM uses QDM version 5.6. Please refer to the eCQI resource center (https://ecqi.healthit.gov/qdm) for more information on the QDM.

Patient Group Definitions

Group Description Instructions Links
Initial PopulationAll patients aged 18 years and older with two qualifying encounters during the measurement period and a diagnosis of heart failureWebchart Instructions
DenominatorEquals Initial Population with a current or prior LVEF <= 40%Webchart Instructions
Denominator ExclusionsPatients with a history of heart transplant or with a Left Ventricular Assist Device (LVAD) prior to the end of the outpatient encounter with Moderate or Severe LVSDWebchart Instructions
NumeratorPatients who were prescribed or already taking beta-blocker therapy during the measurement periodWebchart Instructions
Numerator ExclusionsNot ApplicableWebchart Instructions
Denominator ExceptionsDocumentation of medical reason(s) for not prescribing beta-blocker therapy (e.g., arrhythmia, asthma, bradycardia, hypotension, patients with atrioventricular block without cardiac pacer, observation of consecutive heart rates <50, allergy, intolerance, other medical reasons). Documentation of patient reason(s) for not prescribing beta-blocker therapy (e.g., patient declined, other patient reasons).Webchart Instructions

Details

Full eMeasure Code eMeasure Identifier Measure Year Version NQF # GUID
CMS144v12 2024 12.0.000 0083e 8439f671-2932-4d4c-88ca-ea5faeacc89a
Steward Developer Endorsed By
American Medical Association (AMA) American Heart Association National Quality Forum
Scoring Method Measure Type Stratification Risk Adjustment
Proportion PROCESS None None

Rate Aggregation

None

Improvement Notation

Higher score indicates better quality

Rationale

Beta blockers improve survival and reduce hospitalization for patients with stable heart failure and reduced LVEF (HFrEF). Treatment should be initiated as soon as a patient is diagnosed with reduced LVEF and does not have prohibitively low systemic blood pressure, fluid overload, or recent treatment with an intravenous positive inotropic agent. Beta blockers have also been shown to lessen the symptoms of heart failure, improve the clinical status of patients, and reduce future clinical deterioration. Despite these benefits, use of beta blockers in eligible patients remains suboptimal.

Clinical Recommendation Statement

In patients with HFrEF, with current or previous symptoms, use of 1 of the 3 beta blockers proven to reduce mortality (e.g., bisoprolol, carvedilol, sustained-release metoprolol succinate) is recommended to reduce mortality and hospitalizations (Class I, Level of Evidence A) (ACC/AHA/HFSA, 2022). 

Drugs Commonly Used for Stage C HFrEF (abbreviated to align with focus of measure to include only Beta-blocker therapy)
Drug                               Initial Daily Dose(s)       Target Dose(s)        Mean Doses Achieved in Clinical Trials
                                                                                                                                                
Beta Blockers
Bisoprolol                         1.25 mg once               10 mg once                  8.6 mg/d
Carvedilol                         3.125 mg twice            25-50 mg twice             37 mg/d
Carvedilol CR                  10 mg once                  80 mg once                   N/A
Metoprolol succinate        12.5 to 25 mg once      200 mg once                159 mg/d
extended release
(metoprolol CR/XL)

Definition

LVEF <=40% corresponds to qualitative documentation of moderate dysfunction or severe dysfunction (LVSD). The LVSD may be determined by quantitative or qualitative assessment, which may be current or historical. Examples of a quantitative or qualitative assessment may include an echocardiogram: 1) that provides a numerical value of LVSD or 2) that uses descriptive terms such as moderately or severely depressed left ventricular systolic function. Any current or prior ejection fraction study documenting LVSD can be used to identify patients.

Transmission Format

TBD

Applicable Value Sets

Category Value Set OID
Allergy/Intolerance Beta Blocker Therapy Ingredient 2.16.840.1.113883.3.526.3.1493
Diagnosis Allergy to Beta Blocker Therapy 2.16.840.1.113883.3.526.3.1177
Diagnosis Arrhythmia 2.16.840.1.113883.3.526.3.366
Diagnosis Asthma 2.16.840.1.113883.3.526.3.362
Diagnosis Atrioventricular Block 2.16.840.1.113883.3.526.3.367
Diagnosis Bradycardia 2.16.840.1.113883.3.526.3.412
Diagnosis Cardiac Pacer in Situ 2.16.840.1.113883.3.526.3.368
Diagnosis Heart Failure 2.16.840.1.113883.3.526.3.376
Diagnosis Heart Transplant Related Diagnoses 2.16.840.1.113762.1.4.1178.56
Diagnosis Hypotension 2.16.840.1.113883.3.526.3.370
Diagnosis Intolerance to Beta Blocker Therapy 2.16.840.1.113883.3.526.3.1178
Diagnosis Left Ventricular Assist Device Related Diagnoses 2.16.840.1.113762.1.4.1178.58
Diagnosis Moderate or Severe LVSD 2.16.840.1.113883.3.526.3.1090
Diagnostic Study, Performed Ejection Fraction 2.16.840.1.113883.3.526.3.1134
Encounter, Performed Care Services in Long-Term Residential Facility 2.16.840.1.113883.3.464.1003.101.12.1014
Encounter, Performed Home Healthcare Services 2.16.840.1.113883.3.464.1003.101.12.1016
Encounter, Performed Nursing Facility Visit 2.16.840.1.113883.3.464.1003.101.12.1012
Encounter, Performed Office Visit 2.16.840.1.113883.3.464.1003.101.12.1001
Encounter, Performed Outpatient Consultation 2.16.840.1.113883.3.464.1003.101.12.1008
Encounter, Performed Patient Provider Interaction 2.16.840.1.113883.3.526.3.1012
Medication, Active Beta Blocker Therapy for LVSD 2.16.840.1.113883.3.526.3.1184
Medication, Not Ordered Beta Blocker Therapy for LVSD 2.16.840.1.113883.3.526.3.1184
Medication, Order Beta Blocker Therapy for LVSD 2.16.840.1.113883.3.526.3.1184
Patient Characteristic Ethnicity Ethnicity 2.16.840.1.114222.4.11.837
Patient Characteristic Payer Payer 2.16.840.1.114222.4.11.3591
Patient Characteristic Race Race 2.16.840.1.114222.4.11.836
Patient Characteristic Sex ONC Administrative Sex 2.16.840.1.113762.1.4.1
Physical Exam, Performed Heart Rate 2.16.840.1.113883.3.526.3.1176
Procedure, Performed Cardiac Pacer 2.16.840.1.113762.1.4.1178.53
Procedure, Performed Heart Transplant 2.16.840.1.113762.1.4.1178.33
Procedure, Performed Left Ventricular Assist Device Placement 2.16.840.1.113762.1.4.1178.61

References

CITATIONHeidenreich, P.A., Bozkurt, B, Aguilar, D., ... Allen, L. A. (2022). 2022 AHA/ACC/HFSA Guideline for the Management of Heart Failure A report of the American College of Cardiology/American Heart Association Joint Committee on Clinical Practice Guidelines. Circulation, 145(18), e895-e1032. doi: 10.1161/CIR.0000000000001063

Disclaimer

The Measure is not a clinical guideline, does not establish a standard of medical care, and has not been tested for all potential applications. The Measure, while copyrighted, can be reproduced and distributed, without modification, for noncommercial purposes, e.g., use by health care providers in connection with their practices. Commercial use is defined as the sale, license, or distribution of the Measure for commercial gain, or incorporation of the Measure into a product or service that is sold, licensed or distributed for commercial gain. Commercial uses of the Measure require a license agreement between the user and the American College of Cardiology (ACC) or the American Heart Association (AHA). Neither the ACC, nor AHA, nor their members shall be responsible for any use of the Measure. ACC and AHA encourage use of the Measure by other health care professionals, where appropriate. THE MEASURE AND SPECIFICATIONS ARE PROVIDED "AS IS" WITHOUT WARRANTY OF ANY KIND. Limited proprietary coding is contained in the Measure specifications for convenience. Users of the proprietary code sets should obtain all necessary licenses from the owners of these code sets. The ACC and AHA and their members disclaim all liability for use or accuracy of any Current Procedural Terminology (CPT[R]) or other coding contained in the specifications. CPT(R) contained in the Measure specifications is copyright 2004-2022 American Medical Association. LOINC(R) is copyright 2004-2022 Regenstrief Institute, Inc. This material contains SNOMED Clinical Terms(R) (SNOMED CT[R]) copyright 2004-2022 International Health Terminology Standards Development Organisation. ICD-10 is copyright 2022 World Health Organization. All Rights Reserved. The American Medical Association’s and the PCPI(R) Foundation’s significant past efforts and contributions to the performance measure are gratefully acknowledged. Due to technical limitations, registered trademarks are indicated by (R) or [R].

Copyright

Copyright 2023 American College of Cardiology and American Heart Association. All Rights Reserved.

Source: https://ecqi.healthit.gov/ecqm/measures/cmsv1