<?xml version="1.0"?>
<response><item key="0"><views_conditional_field>2024 Performance Period</views_conditional_field><field_cms_id>CMS145v12</field_cms_id><field_short_name></field_short_name><field_nqf>0070e</field_nqf><field_quality_id>007</field_quality_id><body><![CDATA[<p>Percentage of patients aged 18 years and older with a diagnosis of coronary artery disease seen within a 12-month period who also have a prior MI or a current or prior LVEF &lt;=40% who were prescribed beta-blocker therapy</p>]]></body><field_definition><![CDATA[<div class="photoswipe-gallery"><p>Prescribed may include prescription given to the patient for beta-blocker therapy at one or more visits in the measurement period OR patient already taking beta-blocker therapy as documented in current medication list.</p><p>Prior Myocardial Infarction (MI) for <a href="/glossary/denominator" title="The denominator is the lower part of a fraction used to calculate a rate, proportion, or ratio. It can be the same as the initial population or a subset of the initial population to further constrain the population for the purpose of the measure. Continuous variable measures do not have a denominator, but instead define a measure population. " class="glossify-tooltip-link">denominator</a> 2 is limited to those occurring within the past 3 years.</p><p>LVEF &lt;= 40% corresponds to qualitative documentation of moderate dysfunction or severe dysfunction (LVSD). The LVSD may be determined by quantitative or <a href="/glossary/qualitative-assessment" title="A qualitative assessment uses approaches such as focus groups, in-depth interviews, detailed behavioral observations, or analysis of written or spoken text, typically to gain an understanding of motivations or opinions. " class="glossify-tooltip-link">qualitative assessment</a>, which may be current or historical. Examples of a quantitative or qualitative assessment may include an echocardiogram:</p><p>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.</p></div>]]></field_definition><field_initial_patient_population><![CDATA[<div class="photoswipe-gallery"><p>All patients aged 18 years and older with two qualifying encounters during the measurement period and a diagnosis of coronary artery disease</p></div>]]></field_initial_patient_population><field_measurepopulationexclusion></field_measurepopulationexclusion><field_numerator_state><![CDATA[<div class="photoswipe-gallery"><p>Patients who were prescribed beta-blocker therapy</p></div>]]></field_numerator_state><field_numerator_exclusions><![CDATA[<div class="photoswipe-gallery"><p>Not Applicable</p></div>]]></field_numerator_exclusions><field_denominator_statement><![CDATA[<div class="photoswipe-gallery"><p>Equals Initial Population who also have prior (within the past 3 years) MI or a current or prior LVEF &lt;=40%</p></div>]]></field_denominator_statement><field_denominator_exclusions><![CDATA[<div class="photoswipe-gallery"><p>None</p></div>]]></field_denominator_exclusions><field_denominator_exceptions><![CDATA[<div class="photoswipe-gallery"><p>Documentation 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 &lt;50, allergy, intolerance, other medical reasons).</p><p>Documentation of patient reason(s) for not prescribing beta-blocker therapy (e.g., patient declined, other patient reasons).</p></div>]]></field_denominator_exceptions><field_measure_steward><![CDATA[<a href="/measure-stewards/american-heart-association" hreflang="en">American Heart Association</a>]]></field_measure_steward><field_measuredeveloper></field_measuredeveloper><field_measure_score><![CDATA[<a href="/ecqm-measure-scoring/proportion" hreflang="en">Proportion</a>]]></field_measure_score><field_score_type><![CDATA[<a href="/ecqm-type/process" hreflang="en">Process</a>]]></field_score_type><field_improvement_notation><![CDATA[<div class="photoswipe-gallery"><p>Higher score indicates better quality</p></div>]]></field_improvement_notation><field_guidance><![CDATA[Beta-blocker therapy:- For patients with prior MI, beta-blocker therapy includes any agent within the beta-blocker drug class. As of 2015, no recommendations or evidence are cited in current stable ischemic heart disease guidelines for preferential use of specific agents- For patients with prior LVEF &lt;=40%, beta-blocker therapy includes the following: bisoprolol, carvedilol, or sustained release metoprolol succinateThe requirement of two or more visits is to establish that the eligible professional or eligible clinician has an existing relationship with the patient.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."If a patient has had a myocardial infarction (MI) within the past 3 years and a current or prior LVEF &lt;=40% (or moderate or severe LVSD), the patient should only be counted in Population Criteria 1.This eCQM is a patient-based measure.This version of the eCQM uses QDM version 5.6. Please refer to the QDM page for more information on the QDM.]]></field_guidance><field_telehealth_eligible>Yes</field_telehealth_eligible><field_rationale><![CDATA[<div class="photoswipe-gallery"><p>For patients with coronary artery disease (CAD), beta-blockers are recommended for 3 years after myocardial infarction or acute coronary syndrome. Beta-blockers, particularly carvedilol, metoprolol succinate, or bisoprolol which have been shown to reduce risk of death, are recommended indefinitely for patients with CAD and LV systolic dysfunction. These agents have proven efficacy in reducing angina onset and improving the ischemic threshold during exercise. In patients who have suffered an MI, beta-blockers significantly reduce deaths and recurrent MIs (ACCF/AHA/ACP/AATS/PCNA/SCAI/STS, 2012).</p><p>Nonadherence to cardioprotective medications is prevalent among outpatients with CAD and can be associated with a broad range of adverse outcomes, including all-cause and cardiovascular mortality, cardiovascular hospitalizations, and the need for revascularization procedures (ACC/AHA, 2002).</p><p>This measure is intended to promote beta-blocker usage in select patients with CAD.</p></div>]]></field_rationale><field_stratification><![CDATA[<div class="photoswipe-gallery"><p>None</p></div>]]></field_stratification><field_riskadjustment><![CDATA[<div class="photoswipe-gallery"><p>None</p></div>]]></field_riskadjustment><field_clinicalrecommendationstat><![CDATA[<div class="photoswipe-gallery"><p>Beta-blocker therapy should be started and continued for 3 years in all patients with normal LV function after MI or ACS (Class I, Level of Evidence: B) (ACCF/AHA/ACP/AATS/PCNA/SCAI/STS, 2012).</p><p>Beta-blocker therapy should be used in all patients with LV systolic dysfunction (EF &lt;= 40%) with heart failure or prior MI, unless contraindicated. (Use should be limited to carvedilol, metoprolol succinate, or bisoprolol, which have been shown to reduce risk of death.) (Class I, Level of Evidence: A) (ACCF/AHA/ACP/AATS/PCNA/SCAI/STS, 2012).</p></div>]]></field_clinicalrecommendationstat><field_addendum_notes></field_addendum_notes></item><item key="1"><views_conditional_field>2025 Performance Period</views_conditional_field><field_cms_id>CMS145v13</field_cms_id><field_short_name></field_short_name><field_nqf>0070e</field_nqf><field_quality_id>007</field_quality_id><body><![CDATA[<p>Percentage of patients aged 18 years and older with a diagnosis of coronary artery disease seen within a 12-month period who also have a prior MI or a current or prior left ventricular ejection fraction (LVEF) &lt;=40% who were prescribed beta-blocker therapy</p>]]></body><field_definition><![CDATA[<p>Prescribed may include prescription given to the patient for beta-blocker therapy at one or more visits in the measurement period OR patient already taking beta-blocker therapy as documented in current medication list.</p><p>Prior Myocardial Infarction (MI) for denominator 2 is limited to those occurring within the past 3 years.</p><p>LVEF &lt;= 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:</p><p>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.</p>]]></field_definition><field_initial_patient_population><![CDATA[<p>All patients aged 18 years and older with two qualifying encounters during the measurement period and a diagnosis of coronary artery disease</p>]]></field_initial_patient_population><field_measurepopulationexclusion></field_measurepopulationexclusion><field_numerator_state><![CDATA[<p>Patients who were prescribed beta-blocker therapy</p>]]></field_numerator_state><field_numerator_exclusions><![CDATA[<p>Not Applicable</p>]]></field_numerator_exclusions><field_denominator_statement><![CDATA[<p>Equals Initial Population who also have prior (within the past 3 years) MI or a current or prior LVEF &lt;=40%</p>]]></field_denominator_statement><field_denominator_exclusions><![CDATA[<p>None</p>]]></field_denominator_exclusions><field_denominator_exceptions><![CDATA[<p>Documentation 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 &lt;50, allergy, intolerance, other medical reasons).</p><p>Documentation of patient reason(s) for not prescribing beta-blocker therapy (e.g., patient declined, other patient reasons).</p>]]></field_denominator_exceptions><field_measure_steward><![CDATA[<a href="/measure-stewards/american-heart-association" hreflang="en">American Heart Association</a>]]></field_measure_steward><field_measuredeveloper></field_measuredeveloper><field_measure_score><![CDATA[<a href="/ecqm-measure-scoring/proportion" hreflang="en">Proportion</a>]]></field_measure_score><field_score_type><![CDATA[<a href="/ecqm-type/process" hreflang="en">Process</a>]]></field_score_type><field_improvement_notation><![CDATA[<p>Higher score indicates better quality</p>]]></field_improvement_notation><field_guidance><![CDATA[Beta-blocker therapy:- For patients with prior MI, beta-blocker therapy includes any agent within the beta-blocker drug class. As of 2015, no recommendations or evidence are cited in current stable ischemic heart disease guidelines for preferential use of specific agents.- For patients with prior LVEF &lt;=40%, beta-blocker therapy includes the following: bisoprolol, carvedilol, or sustained release metoprolol succinate.The requirement of two or more visits is to establish that the eligible clinician has an existing relationship with the patient.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."If a patient has had a myocardial infarction (MI) within the past 3 years and a current or prior LVEF &lt;=40% (or moderate or severe LVSD), the patient should only be counted in Population Criteria 1.This eCQM is a patient-based measure.This version of the eCQM uses QDM version 5.6. Please refer to the QDM page for more information on the QDM.]]></field_guidance><field_telehealth_eligible>Yes</field_telehealth_eligible><field_rationale><![CDATA[<p>For patients with coronary artery disease (CAD), beta-blockers are recommended for 3 years after myocardial infarction or acute coronary syndrome. Beta-blockers, particularly carvedilol, metoprolol succinate, or bisoprolol which have been shown to reduce risk of death, are recommended indefinitely for patients with CAD and LV systolic dysfunction. These agents have proven efficacy in reducing angina onset and improving the ischemic threshold during exercise. In patients who have suffered an MI, beta-blockers significantly reduce deaths and recurrent MIs (Fihn et al., 2012).</p><p>Nonadherence to cardioprotective medications is prevalent among outpatients with CAD and can be associated with a broad range of adverse outcomes, including all-cause and cardiovascular mortality, cardiovascular hospitalizations, and the need for revascularization procedures (Gibbons et al., 2002).</p><p>This measure is intended to promote beta-blocker usage in select patients with CAD.</p>]]></field_rationale><field_stratification><![CDATA[<p>None</p>]]></field_stratification><field_riskadjustment><![CDATA[<p>None</p>]]></field_riskadjustment><field_clinicalrecommendationstat><![CDATA[<p>Beta-blocker therapy should be started and continued for 3 years in all patients with normal LV function after MI or acute coronary syndrome (ACS) (Class I, Level of Evidence: B) (Fihn et al., 2012).</p><p>Beta-blocker therapy should be used in all patients with LV systolic dysfunction (EF &lt;= 40%) with heart failure or prior MI, unless contraindicated. (Use should be limited to carvedilol, metoprolol succinate, or bisoprolol, which have been shown to reduce risk of death.) (Class I, Level of Evidence: A) (Fihn et al., 2012).</p><p>In patients with chronic coronary disease (CCD) and LVEF ≤40% with or without previous MI, the use of beta-blocker therapy is recommended to reduce the risk of future Major Adverse Cardiac Events (MACE), including cardiovascular death. (Class 1, Level of Evidence: A) (Virani et al., 2023)</p>]]></field_clinicalrecommendationstat><field_addendum_notes></field_addendum_notes></item><item key="2"><views_conditional_field>2026 Performance Period</views_conditional_field><field_cms_id>CMS145v14</field_cms_id><field_short_name></field_short_name><field_nqf>0070e</field_nqf><field_quality_id>007</field_quality_id><body><![CDATA[<p>Percentage of patients aged 18 years and older with a diagnosis of coronary artery disease seen within a 12-month period who also have a prior MI or a current or prior left ventricular ejection fraction (LVEF) &lt;=40% who were prescribed beta-blocker therapy</p>]]></body><field_definition><![CDATA[<p>Prescribed may include prescription given to the patient for beta-blocker therapy at one or more visits in the measurement period OR patient already taking beta-blocker therapy as documented in current medication list.</p><p>Prior Myocardial Infarction (MI) for denominator 2 is limited to those occurring within the past 3 years.</p><p>LVEF &lt;= 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:</p><p>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.</p>]]></field_definition><field_initial_patient_population><![CDATA[<p>All patients aged 18 years and older with two qualifying encounters during the measurement period and a diagnosis of coronary artery disease</p>]]></field_initial_patient_population><field_measurepopulationexclusion></field_measurepopulationexclusion><field_numerator_state><![CDATA[<p>Patients who were prescribed beta-blocker therapy</p>]]></field_numerator_state><field_numerator_exclusions><![CDATA[<p>None</p>]]></field_numerator_exclusions><field_denominator_statement><![CDATA[<p>Equals Initial Population who also have prior (within the past 3 years) MI or a current or prior LVEF &lt;=40%</p>]]></field_denominator_statement><field_denominator_exclusions><![CDATA[<p>None</p>]]></field_denominator_exclusions><field_denominator_exceptions><![CDATA[<p>Documentation 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 &lt;50, allergy, intolerance, other medical reasons).</p><p>Documentation of patient reason(s) for not prescribing beta-blocker therapy (e.g., patient declined, other patient reasons).</p>]]></field_denominator_exceptions><field_measure_steward><![CDATA[<a href="/measure-stewards/american-heart-association" hreflang="en">American Heart Association</a>]]></field_measure_steward><field_measuredeveloper></field_measuredeveloper><field_measure_score><![CDATA[<a href="/ecqm-measure-scoring/proportion" hreflang="en">Proportion</a>]]></field_measure_score><field_score_type><![CDATA[<a href="/ecqm-type/process" hreflang="en">Process</a>]]></field_score_type><field_improvement_notation><![CDATA[<p>Higher score indicates better quality</p>]]></field_improvement_notation><field_guidance><![CDATA[Beta-blocker therapy:- For patients with prior MI, beta-blocker therapy includes any agent within the beta-blocker drug class. As of 2015, no recommendations or evidence are cited in current stable ischemic heart disease guidelines for preferential use of specific agents.- For patients with prior LVEF &lt;=40%, beta-blocker therapy includes the following: bisoprolol, carvedilol, or sustained release metoprolol succinate.The requirement of two or more visits is to establish that the eligible clinician has an existing relationship with the patient.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."If a patient has had a myocardial infarction (MI) within the past 3 years and a current or prior LVEF &lt;=40% (or moderate or severe LVSD), the patient should only be counted in Population Criteria 1.This eCQM is a patient-based measure.This version of the eCQM uses QDM version 5.6. Please refer to the QDM page for more information on the QDM.]]></field_guidance><field_telehealth_eligible>Yes</field_telehealth_eligible><field_rationale><![CDATA[<p>For patients with coronary artery disease (CAD), beta-blockers are recommended for 3 years after myocardial infarction or acute coronary syndrome. Beta-blockers, particularly carvedilol, metoprolol succinate, or bisoprolol which have been shown to reduce risk of death, are recommended indefinitely for patients with CAD and LV systolic dysfunction. These agents have proven efficacy in reducing angina onset and improving the ischemic threshold during exercise. In patients who have suffered an MI, beta-blockers significantly reduce deaths and recurrent MIs (Fihn et al., 2012).</p><p>Nonadherence to cardioprotective medications is prevalent among outpatients with CAD and can be associated with a broad range of adverse outcomes, including all-cause and cardiovascular mortality, cardiovascular hospitalizations, and the need for revascularization procedures (Gibbons et al., 2002).</p><p>This measure is intended to promote beta-blocker usage in select patients with CAD.</p>]]></field_rationale><field_stratification><![CDATA[<p>None</p>]]></field_stratification><field_riskadjustment><![CDATA[<p>None</p>]]></field_riskadjustment><field_clinicalrecommendationstat><![CDATA[<p>Beta-blocker therapy should be started and continued for 3 years in all patients with normal LV function after MI or acute coronary syndrome (ACS) (Class I, Level of Evidence: B) (Fihn et al., 2012).</p><p>Beta-blocker therapy should be used in all patients with LV systolic dysfunction (EF &lt;= 40%) with heart failure or prior MI, unless contraindicated. (Use should be limited to carvedilol, metoprolol succinate, or bisoprolol, which have been shown to reduce risk of death.) (Class I, Level of Evidence: A) (Fihn et al., 2012).</p><p>In patients with chronic coronary disease (CCD) and LVEF ≤40% with or without previous MI, the use of beta-blocker therapy is recommended to reduce the risk of future Major Adverse Cardiac Events (MACE), including cardiovascular death. (Class 1, Level of Evidence: A) (Virani et al., 2023)</p>]]></field_clinicalrecommendationstat><field_addendum_notes></field_addendum_notes></item></response>
