eCQM Title | Statin Therapy for the Prevention and Treatment of Cardiovascular Disease |
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eCQM Identifier (Measure Authoring Tool) | 347 | eCQM Version Number | 8.1.000 |
CBE Number | Not Applicable | GUID | 5375d6a9-203b-4fff-b851-afa9b68d2ac2 |
Measurement Period | January 1, 20XX through December 31, 20XX | ||
Measure Steward | Centers for Medicare & Medicaid Services (CMS) | ||
Measure Developer | Mathematica | ||
Endorsed By | None | ||
Description |
Percentage of the following patients - all considered at high risk of cardiovascular events - who were prescribed or were on statin therapy during the measurement period: - All patients who were previously diagnosed with or currently have a diagnosis of clinical atherosclerotic cardiovascular disease (ASCVD), including an ASCVD procedure; OR - Patients aged 20 to 75 years who have ever had a low-density lipoprotein cholesterol (LDL-C) level >= 190 mg/dL or were previously diagnosed with or currently have an active diagnosis of familial hypercholesterolemia; OR - Patients aged 40-75 years with a diagnosis of diabetes; OR - Patients aged 40 to 75 with a 10-year ASCVD risk score of >= 20 percent. |
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Copyright |
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. CPT(R) contained in the Measure specifications is copyright 2004-2023 American Medical Association. LOINC(R) is copyright 2004-2023 Regenstrief Institute, Inc. This material contains SNOMED Clinical Terms(R) (SNOMED CT[R]) copyright 2004-2023 International Health Terminology Standards Development Organisation. ICD-10 is copyright 2023 World Health Organization. All Rights Reserved. |
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Disclaimer |
These performance measures are not clinical guidelines and do not establish a standard of medical care, and have not been tested for all potential applications. THE MEASURES AND SPECIFICATIONS ARE PROVIDED "AS IS" WITHOUT WARRANTY OF ANY KIND. Due to technical limitations, registered trademarks are indicated by (R) or [R] and unregistered trademarks are indicated by (TM) or [TM]. |
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Measure Scoring | Proportion | ||
Measure Type | Process | ||
Stratification |
None |
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Risk Adjustment |
None |
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Rate Aggregation |
This measure is intended to have one reporting rate, which aggregates the following populations into a single performance rate for reporting purposes: Population 1: All patients who were previously diagnosed with or currently have a diagnosis of clinical ASCVD, including an ASCVD procedure. Population 2: Patients aged 20 to 75 years at the beginning of the measurement period who have ever had a laboratory result of LDL-C >= 190 mg/dL or were previously diagnosed with or currently have an active diagnosis of familial hypercholesterolemia. Population 3: Patients aged 40 to 75 years at the beginning of the measurement period with an active diagnosis of Type 1 or Type 2 diabetes at any time during the measurement period. Population 4: Patients aged 40 to 75 at the beginning of the measurement period with a 10-year ASCVD risk score of > = 20 percent during the measurement period. For the purposes of this measure, a single performance rate can be calculated as follows: Performance Rate = (Numerator 1 + Numerator 2 + Numerator 3 + Numerator 4)/ [(Denominator 1 - Denominator Exclusions 1- Denominator Exceptions 1) + (Denominator 2 - Denominator Exclusions 2 - Denominator Exceptions 2) + (Denominator 3 - Denominator Exclusions 3 - Denominator Exceptions 3) + (Denominator 4 - Denominator Exclusions 4 - Denominator Exceptions 4)] |
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Rationale |
"Cardiovascular disease (CVD) is the leading cause of death in the United States, causing approximately 1 of every 3 deaths in the United States in 2015. In 2015, stroke caused approximately 1 of every 19 deaths in the United States and the estimated annual costs for CVD and stroke were $329.7 billion, including $199.2 billion in direct costs (hospital services, physicians and other professionals, prescribed medications, home health care, and other medical durables) and $130.5 billion in indirect costs from lost future productivity (cardiovascular and stroke premature deaths). CVD costs more than any other diagnostic group" (Benjamin et al., 2018). Data collected between 2011 and 2014 indicates that more than 94.6 million U.S. adults, 20 years or older, had total cholesterol levels equal to 200 mg/dL or more, while almost 28.5 million had levels 240 mg/dL or more (Benjamin et al., 2018). Elevated blood cholesterol is a major risk factor for CVD and statin therapy has been associated with a reduced risk of CVD. Numerous randomized trials have demonstrated that treatment with a statin reduces LDL-C and reduces the risk of major cardiovascular events by approximately 20 percent (Ference, 2015). In 2018, updated guidelines on the treatment of blood cholesterol to reduce atherosclerotic cardiovascular risk in adults were published (Grundy et al., 2019). This guideline was published by an Expert Panel, which synthesized evidence from randomized controlled trials to identify people most likely to benefit from cholesterol-lowering therapy. The American College of Cardiology (ACC)/American Heart Association (AHA)/Multi-society (MS) Guideline recommendations are intended to provide a strong evidence-based foundation for the treatment of blood cholesterol for the primary and secondary prevention and treatment of ASCVD in patients of all ages. The document concludes that the addition of statin therapy reduces the risk of ASCVD among high-risk individuals, defined as follows: individuals with clinical ASCVD, with LDL-C >= 190 mg/dL, with diabetes, or individuals with >= 20 percent risk of ASCVD as determined via use of an ASCVD risk estimator derived from the Pooled Cohort Equations (Grundy et al., 2019). One study surveying U.S. cardiology, primary care, and endocrinology practices found that 1 in 4 guideline-eligible patients were not on a statin and less than half were on the recommended statin intensity. Untreated and undertreated patients had significantly higher LDL-C levels than those receiving guideline-directed statin treatment (Navar et al., 2017). In a follow-up study authored by Nanna et al., the same clinics were divided into tertiles based on the percentage of patients with guideline-recommended statin use. The researchers found that patients in the high-tertile clinics were more likely to achieve target LDL-C levels than patients at the low- or mid-tertile clinics, and this held true when patients were stratified by primary and secondary prevention (Nanna et al., 2019a). Research also indicates that certain populations are far less likely to receive guideline-recommended statin therapy than others. A retrospective study of the National Health and Nutrition Examination Survey found that Black and Hispanic race or ethnicity, low income, lack of health insurance coverage, poor health care access, young age, and female gender are predictors of lower statin utilization (Gu et al., 2018). In particular, there is extensive evidence that women are far less likely than men to be prescribed guideline-recommended statin therapy (Nanna et al., 2019b), despite research showing that female patients with cardiovascular disease derive the same or greater benefit from statin therapy as male patients with cardiovascular disease (Puri et al., 2014). The Statin Safety Expert Panel that participated in a National Lipid Association (NLA) Statin Safety Task Force meeting in October 2013 reaffirms the general safety of statin therapy. The panel members concluded that for most patients requiring statin therapy, the potential benefits of statin therapy outweigh the potential risks. In general terms, the benefits of statins to prevent non-fatal myocardial infarction, revascularization, stroke, and CVD mortality, far outweigh any potential harm related to the drug (Jacobson, 2014). |
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Clinical Recommendation Statement |
This electronic clinical quality measure is intended to align with the 2018 ACC/AHA/MS Guideline on the Management of Blood Cholesterol (Grundy et al., 2019), which indicates the use of statins as the first line of cholesterol-lowering medication therapy to lower the risk of ASCVD among at-risk populations. Recommendations for Management of Blood Cholesterol to Reduce Atherosclerotic Cardiovascular Risk in Adults - Statin Treatment: Secondary Prevention: 1. In patients who are 75 years of age or younger with clinical ASCVD, high-intensity statin therapy should be initiated or continued with the aim of achieving a 50 percent or greater reduction in LDL-C levels (Class I Recommendation), (Grundy et al., 2019). 2. In patients with clinical ASCVD in whom high-intensity statin therapy is contraindicated or who experience statin-associated side effects, moderate-intensity statin therapy should be initiated or continued with the aim of achieving a 30 to 49 percent reduction in LDL-C levels (Class I Recommendation), (Grundy et al., 2019). 3. In patients older than 75 years of age with clinical ASCVD, it is reasonable to initiate moderate- or high-intensity statin therapy after evaluation of the potential for ASCVD risk reduction, adverse effects, and drug–drug interactions, as well as patient frailty and patient preferences (Class IIa Recommendation), (Grundy et al., 2019). Primary Prevention 1. In patients 20 to 75 years of age with an LDL-C level of 190 mg/dL or higher (>= 4.9 mmol/L), maximally tolerated statin therapy is recommended. (Class I Recommendation), (Grundy et al., 2019). 2. In adults 40 to 75 years of age with diabetes mellitus, regardless of estimated 10-year ASCVD risk, moderate-intensity statin therapy is indicated (Class I Recommendation), (Grundy et al., 2019). 3. To facilitate decisions about preventive interventions, it is recommended to screen for traditional ASCVD risk factors and apply the race- and sex-specific Pooled Cohort Equations (PCE) to estimate 10-year ASCVD risk for asymptomatic adults 40 to 75 years of age. The higher the estimated risk, the more likely the patient is to benefit from statin treatment (Grundy et al., 2019). The US Preventive Services Task Force (USPSTF) concludes with moderate certainty that statin use for the prevention of CVD events and all-cause mortality in adults aged 40 to 75 years with no history of CVD and who have 1 or more of these CVD risk factors and an estimated 10-year CVD event risk of 7.5 percent to less than 10 percent has at least a small net benefit (USPSTF 2022). Statin Safety and Statin-Associated Side Effects A clinician–patient risk discussion is recommended before initiation of statin therapy to review net clinical benefit, weighing the potential for ASCVD risk reduction against the potential for statin-associated side effects, statin–drug interactions, and safety, while emphasizing that side effects can be addressed successfully (Class I Recommendation), (Grundy et al., 2019). |
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Improvement Notation |
Higher score indicates better quality |
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Reference |
Reference Type: CITATION Reference Text: 'Benjamin, E. J., Virani, S. S., Callaway, C. W., Chamberlain, A. M., Chang, A. R., Cheng, S., …Munter, P. (2018). Heart disease and stroke statistics—2018 update: A report from the American Heart Association. Circulation, 137(12), e67-e492. doi.10.1161/CIR.0000000000000558' |
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Reference |
Reference Type: CITATION Reference Text: 'Ference, B.A. (2015). Statins and the risk of developing new-onset Type 2 diabetes: Expert analysis. Retrieved from https://www.acc.org/latest-in-cardiology/articles/2015/03/10/08/10/statins-and-the-risk-of-developing-new-onset-type-2-diabetes' |
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Reference |
Reference Type: CITATION Reference Text: 'Grundy, S. M., Stone, N. J., Bailey, A. L., Beam, C., Birtcher, K. K., Blumenthal, R. S., Braun, L. T., …Yeboah, J. (2019) 2018 AHA/ACC/AACVPR/AAPA/ABC/ACPM/ADA/AGS/APhA/ASPC/NLA/PCNA Guideline on the Management of Blood Cholesterol. Journal of the American College of Cardiology, 73(24), e286-e343. doi.10.1016/j.jacc.2018.11.003' |
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Reference |
Reference Type: CITATION Reference Text: 'Gu, A., Kamat, S., Argulian, E. (2018). Trends and disparities in statin use and low-density lipoprotein cholesterol levels among US patients with diabetes, 1999–2014. Diabetes Research and Clinical Practice, 139, 1-10. doi:10.1016/j.diabres.2018.02.019' |
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Reference |
Reference Type: CITATION Reference Text: 'Jacobson, T. A. (2014). Executive summary: NLA Task Force on Statin Safety—2014 update. Journal of Clinical Lipidology, 8(3 Suppl.), S1-S4. doi:10.1016/jacl.2014.03.002' |
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Reference |
Reference Type: CITATION Reference Text: 'Nanna, M. G., Navar, A. M., Wang, Y. T., Li, S., Virani, S. S., Li, Z., … Peterson, E. D. (2019a). Practice-Level Variation in Statin use and Low-Density Lipoprotein Cholesterol Control in the United States: Results from the Patient and Provider Assessment of Lipid Management (PALM) Registry. American Heart Journal, 214, 113–124. doi:10.1016/j.ahj.2019.05.009' |
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Reference |
Reference Type: CITATION Reference Text: 'Nanna, M. G., Wang, T. Y., Xiang, Q., Goldberg, A. C., Robinson, J. G., Roger, V. L., … Navar, A. M. (2019b). Sex Differences in the use of Statins in Community Practice. Circulation. Cardiovascular Quality & Outcomes, 12(8), e005562. doi:10.1161/CIRCOUTCOMES.118.005562' |
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Reference |
Reference Type: CITATION Reference Text: 'Navar, M., Wang, T. Y., Li, S.,Robinson, J. G., Goldberg, A. C., Virani, S., …Peterson, E. D. (2017). Lipid management in contemporary community practice: Results from the Provider Assessment of Lipid Management (PALM) Registry. American Heart Journal, 193, 84-92. doi.10.1016/j.ahj.2017.08.005' |
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Reference |
Reference Type: CITATION Reference Text: 'Puri, R., Nissen, S. E., Shao, M., Ballantyne, C. M., Barter, P. J., Chapman, M. J., … Nicholls, S. J. (2014). Sex-related differences of coronary atherosclerosis regression following maximally intensive statin therapy: insights from SATURN. JACC. Cardiovascular imaging, 7(10), 1013–1022. doi:10.1016/j.jcmg.2014.04.019' |
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Reference |
Reference Type: CITATION Reference Text: 'U.S. Preventive Services Task Force (USPSTF) (2022). Statin Use for the Primary Prevention of Cardiovascular Disease in Adults: US Preventive Services Task Force Recommendation Statement. Journal of American Medical Association; 328(8):746-753. doi:10.1001/jama.2022.13044' |
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Definition |
Clinical atherosclerotic cardiovascular disease (ASCVD) includes: - Acute coronary syndromes - History of myocardial infarction - Stable or unstable angina - Coronary or other arterial revascularization - Stroke or transient ischemic attack (TIA) - Peripheral arterial disease of atherosclerotic origin Lipoprotein density cholesterol (LDL-C) result: - A fasting or non-fasting LDL-C laboratory test performed and direct or calculated test result documented in the medical record. When both direct and calculated test results are available on the same day, the direct LDL-C test result should be used. Statin therapy: - Administration of one or more of a group of medications that are used to lower plasma lipoprotein levels in the treatment of hyperlipoproteinemia. Statin Medication Therapy List (NOTE: List does NOT include dosage): [Generic name] (Brand or trade name) and (-) Medication type, if applicable: [Atorvastatin] (Lipitor) - Statin [Fluvastatin] (Lescol XL or Lescol) - Statin [Lovastatin (Mevinolin)](Mevacor or Altoprev) - Statin [Pitavastatin] (Livalo or Zypitamag or Nikita) - Statin [Pravastatin Sodium] (Pravachol) - Statin [Rosuvastatin Calcium] (Crestor) - Statin [Simvastatin] (Zocor) - Statin [Amlodipine Besylate/Atorvastatin Calcium] (Caduet) – Fixed Dose Combination [Ezetimibe / Rosuvastatin] (Roszet) – Fixed Dose Combination [Ezetimibe/Simvastatin] (Vytorin) – Fixed Dose Combination Statin-Associated Muscle Symptoms (SAMS) – The 2018 ACC/AHA/MS Guideline (Grundy et al., 2019) includes the following SAMS: myalgias, myositis, myopathy, or statin-associated autoimmune myopathy. Patients who experience significant or repeated statin-associated muscle symptoms may prefer not to take or continue statin therapy and therefore may be removed from the denominator. |
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Guidance |
Initial Population Guidance: The initial population covers four distinct populations. Use the following process to prevent counting patients more than once. Initial Population 1: All patients who were previously diagnosed with or currently have a diagnosis of clinical ASCVD, including an ASCVD procedure before the end of the measurement period. - If YES, meets Initial Population 1 risk category. - If NO, screen for next risk category. Initial Population 2: Patients aged 20 to 75 years at the beginning of the measurement period who have ever had a laboratory test result of LDL-C >= 190 mg/dL or were previously diagnosed with or currently have an active diagnosis of familial hypercholesterolemia. - If YES, meets Initial Population 2 risk category. - If NO, screen for next risk category. Initial Population 3: Patients aged 40 to 75 years at the beginning of the measurement period with an active diagnosis of Type 1 or Type 2 diabetes at any time during the measurement period. - If YES, meets Initial Population 3 risk category. - If NO, screen for next risk category. Initial Population 4: Patients aged 40 to 75 at the beginning of the measurement period with a 10-year ASCVD risk score of >= 20 percent during the measurement period. - If YES, meets Initial Population 4 risk category. - If NO, patient does NOT meet Initial Population criteria and is NOT eligible for measure inclusion. Initial Population Guidance for Encounter: In order for the patient to be included in the Initial Population, the patient must have ONE initial population-eligible visit, defined as follows: outpatient visit, initial or established office visit, face-to-face interaction, preventive care services, or annual wellness visit. LDL-C Laboratory test result options: The measure can be reported for all patients with a documented LDL-C level recorded as follows: To meet Initial Population 1: There is no LDL-C result required. To meet Initial Population 2: If a patient has ANY previous laboratory result of LDL-C >= 190 mg/dL, report the highest value >= 190 mg/dL. To meet Initial Population 3: There is no LDL-C result required. To meet Initial Population 4: There is no LDL-C result required. The 10-year ASCVD risk assessment options: The 10-year ASCVD risk score is calculated using the Pooled Cohort Equations: 1) the 2013 ACC/AHA ASCVD Risk Estimator (maps to LOINC Code 79423-0) OR 2) the ACC Risk Estimator Plus (maps to LOINC Code 99055-6). If your EHR does not have either of these risk calculators, we recommend that you use the on-line versions. The 10-year ASCVD risk score (quantitative result, i.e., result.value, "%") must be documented in a structured field. The 10-year ASCVD risk assessment must be performed during the measurement period. Numerator instructions and guidance: - Current statin therapy use must be documented in the patient's current medication list or ordered during the measurement period. - ONLY statin therapy meets the measure Numerator criteria (NOT other cholesterol lowering medications). - Prescription or order does NOT need to be linked to an encounter or visit; it may be called to the pharmacy. - Statin medication "samples" provided to patients can be documented as "current statin therapy" if documented in the medication list in health/medical record. - Patients who meet the denominator criteria for inclusion, but are not prescribed or using statin therapy, will NOT meet performance for this measure unless they have an allowable denominator exception. Patients with an allowable denominator exception should be removed from the denominator of the measure and reported as a valid exception. - There is only one performance rate calculated for this measure: the weighted average of the four populations. - Adherence to statin therapy is not calculated in this measure. - It may not be appropriate to prescribe statin therapy for some patients (see exceptions and exclusions for the complete list). Intensity of statin therapy in primary and secondary prevention: The expert panel of the 2018 ACC/AHA/MS Guidelines (Grundy et al., 2019) defines recommended intensity of statin therapy on the basis of the average expected LDL-C response to specific statin and dose. Although intensity of statin therapy is important in managing cholesterol, this measure assesses prescription of ANY statin therapy, irrespective of intensity. Assessment of appropriate intensity and dosage documentation added too much complexity to allow inclusion of statin therapy intensity in the measure at this time. Lifestyle modification coaching: A healthy lifestyle is important for the prevention of cardiovascular disease. However, lifestyle modification monitoring and documentation added too much complexity to allow its inclusion in the measure at this time. Millimoles per liter (mmol/L) should be converted to milligrams per deciliter (mg/dL) for reporting this measure. This eCQM is a patient-based measure. 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. |
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Transmission Format |
TBD |
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Initial Population |
Population 1: All patients who were previously diagnosed with or currently have a diagnosis of clinical ASCVD, including an ASCVD procedure. Population 2: Patients aged 20 to 75 years at the beginning of the measurement period who have ever had a laboratory result of LDL-C >=190 mg/dL or were previously diagnosed with or currently have an active diagnosis of familial hypercholesterolemia. Population 3: Patients aged 40 to 75 years at the beginning of the measurement period with Type 1 or Type 2 diabetes. Population 4: Patients aged 40 to 75 at the beginning of the measurement period with a 10-year ASCVD risk score (i.e., 2013 ACC/AHA ASCVD Risk Estimator or the ACC Risk Estimator Plus) of >= 20 percent during the measurement period. |
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Denominator |
Equals Initial Population |
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Denominator Exclusions |
Patients who are breastfeeding at any time during the measurement period. Patients who have a diagnosis of rhabdomyolysis at any time during the measurement period. |
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Numerator |
Patients who are actively using or who receive an order (prescription) for statin therapy at any time during the measurement period |
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Numerator Exclusions |
Not Applicable |
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Denominator Exceptions |
Patients with statin-associated muscle symptoms or an allergy to statin medication. Patients who are receiving palliative or hospice care. Patients with active liver disease or hepatic disease or insufficiency. Patients with end-stage renal disease (ESRD). Patients with documentation of a medical reason for not being prescribed statin therapy. |
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Supplemental Data Elements |
For every patient evaluated by this measure also identify payer, race, ethnicity and sex |
exists "ASCVD Diagnosis or Procedure before End of Measurement Period" and exists "Qualifying Encounter during Day of Measurement Period"
"Initial Population 1"
exists ( ( ["Diagnosis": "Breastfeeding"] union ["Diagnosis": "Rhabdomyolysis"] ) ExclusionDiagnosis where ExclusionDiagnosis.prevalencePeriod overlaps day of "Measurement Period" )
exists "Statin Therapy Ordered during Measurement Period" or exists "Medication Active during the Measurement Period"
None
"Has Allergy to Statin" or Hospice."Has Hospice Services" or PalliativeCare."Has Palliative Care in the Measurement Period" or "Has Hepatitis or Liver Disease Diagnosis" or "Has Statin Associated Muscle Symptoms" or "Has ESRD Diagnosis" or "Has Adverse Reaction to Statin" or "Has Medical Reason for Not Ordering Statin Therapy"
None
"Patients Age 20 to 75 with LDL Cholesterol Result Greater than or Equal to 190 or Hypercholesterolemia without ASCVD" and exists "Qualifying Encounter during Day of Measurement Period"
"Initial Population 2"
exists ( ( ["Diagnosis": "Breastfeeding"] union ["Diagnosis": "Rhabdomyolysis"] ) ExclusionDiagnosis where ExclusionDiagnosis.prevalencePeriod overlaps day of "Measurement Period" )
exists "Statin Therapy Ordered during Measurement Period" or exists "Medication Active during the Measurement Period"
None
"Has Allergy to Statin" or Hospice."Has Hospice Services" or PalliativeCare."Has Palliative Care in the Measurement Period" or "Has Hepatitis or Liver Disease Diagnosis" or "Has Statin Associated Muscle Symptoms" or "Has ESRD Diagnosis" or "Has Adverse Reaction to Statin" or "Has Medical Reason for Not Ordering Statin Therapy"
None
"Patients Age 40 to 75 Years with Diabetes without ASCVD or LDL Greater than 190 or Hypercholesterolemia" and exists "Qualifying Encounter during Day of Measurement Period"
"Initial Population 3"
exists ( ( ["Diagnosis": "Breastfeeding"] union ["Diagnosis": "Rhabdomyolysis"] ) ExclusionDiagnosis where ExclusionDiagnosis.prevalencePeriod overlaps day of "Measurement Period" )
exists "Statin Therapy Ordered during Measurement Period" or exists "Medication Active during the Measurement Period"
None
"Has Allergy to Statin" or Hospice."Has Hospice Services" or PalliativeCare."Has Palliative Care in the Measurement Period" or "Has Hepatitis or Liver Disease Diagnosis" or "Has Statin Associated Muscle Symptoms" or "Has ESRD Diagnosis" or "Has Adverse Reaction to Statin" or "Has Medical Reason for Not Ordering Statin Therapy"
None
"Patients Age 40 to 75 Years and have a 10 Year CVD Risk of High without ASCVD and High LDL and Diabetes" and exists "Qualifying Encounter during Day of Measurement Period"
"Initial Population 4"
exists ( ( ["Diagnosis": "Breastfeeding"] union ["Diagnosis": "Rhabdomyolysis"] ) ExclusionDiagnosis where ExclusionDiagnosis.prevalencePeriod overlaps day of "Measurement Period" )
exists "Statin Therapy Ordered during Measurement Period" or exists "Medication Active during the Measurement Period"
None
"Has Allergy to Statin" or Hospice."Has Hospice Services" or PalliativeCare."Has Palliative Care in the Measurement Period" or "Has Hepatitis or Liver Disease Diagnosis" or "Has Statin Associated Muscle Symptoms" or "Has ESRD Diagnosis" or "Has Adverse Reaction to Statin" or "Has Medical Reason for Not Ordering Statin Therapy"
None
( ( ["Diagnosis": "Myocardial Infarction"] union ["Diagnosis": "Subsequent non-ST elevation (NSTEMI) myocardial infarction"] union ["Diagnosis": "Cerebrovascular Disease Stroke or TIA"] union ["Diagnosis": "Atherosclerosis and Peripheral Arterial Disease"] union ["Diagnosis": "Ischemic Heart Disease or Related Diagnoses"] union ["Diagnosis": "Stable and Unstable Angina"] ) ASCVDDiagnosis where ASCVDDiagnosis.prevalencePeriod starts on or before day of end of "Measurement Period" ) union ( ( ["Procedure, Performed": "PCI"] union ["Procedure, Performed": "CABG Surgeries"] union ["Procedure, Performed": "Carotid Intervention"] union ["Procedure, Performed": "CABG or PCI Procedure"] ) ASCVDProcedure where Global."NormalizeInterval" ( ASCVDProcedure.relevantDatetime, ASCVDProcedure.relevantPeriod ) starts on or before day of end of "Measurement Period" )
"Initial Population 1"
"Initial Population 2"
"Initial Population 3"
"Initial Population 4"
"Has Allergy to Statin" or Hospice."Has Hospice Services" or PalliativeCare."Has Palliative Care in the Measurement Period" or "Has Hepatitis or Liver Disease Diagnosis" or "Has Statin Associated Muscle Symptoms" or "Has ESRD Diagnosis" or "Has Adverse Reaction to Statin" or "Has Medical Reason for Not Ordering Statin Therapy"
exists ( ( ["Diagnosis": "Breastfeeding"] union ["Diagnosis": "Rhabdomyolysis"] ) ExclusionDiagnosis where ExclusionDiagnosis.prevalencePeriod overlaps day of "Measurement Period" )
exists ["Adverse Event": "Statin Allergen"] StatinReaction where StatinReaction.relevantDatetime during day of "Measurement Period"
exists ["Allergy/Intolerance": "Statin Allergen"] StatinAllergy where StatinAllergy.prevalencePeriod overlaps day of "Measurement Period"
exists ( ["Diagnosis": "Diabetes"] Diabetes where Diabetes.prevalencePeriod overlaps day of "Measurement Period" )
exists ( ["Diagnosis": "End Stage Renal Disease"] ESRD where ESRD.prevalencePeriod overlaps day of "Measurement Period" )
exists ( ( ["Diagnosis": "Hepatitis A"] union ["Diagnosis": "Hepatitis B"] union ["Diagnosis": "Liver Disease"] ) HepatitisLiverDisease where HepatitisLiverDisease.prevalencePeriod overlaps day of "Measurement Period" )
exists ( ( ["Medication, Not Ordered": "Low Intensity Statin Therapy"] union ["Medication, Not Ordered": "Moderate Intensity Statin Therapy"] union ["Medication, Not Ordered": "High Intensity Statin Therapy"] ) NoStatinTherapyOrdered with "Qualifying Encounter during Day of Measurement Period" QualifyingEncounter such that NoStatinTherapyOrdered.authorDatetime during day of QualifyingEncounter.relevantPeriod where NoStatinTherapyOrdered.negationRationale in "Medical Reason" )
exists ( ["Diagnosis": "Statin Associated Muscle Symptoms"] StatinMuscleSymptom where StatinMuscleSymptom.prevalencePeriod overlaps day of "Measurement Period" )
exists ( ["Encounter, Performed": "Encounter Inpatient"] InpatientEncounter where ( InpatientEncounter.dischargeDisposition ~ "Discharge to home for hospice care (procedure)" or InpatientEncounter.dischargeDisposition ~ "Discharge to healthcare facility for hospice care (procedure)" ) and InpatientEncounter.relevantPeriod ends during day of "Measurement Period" ) or exists ( ["Encounter, Performed": "Hospice Encounter"] HospiceEncounter where HospiceEncounter.relevantPeriod overlaps day of "Measurement Period" ) or exists ( ["Assessment, Performed": "Hospice care [Minimum Data Set]"] HospiceAssessment where HospiceAssessment.result ~ "Yes (qualifier value)" and Global."NormalizeInterval" ( HospiceAssessment.relevantDatetime, HospiceAssessment.relevantPeriod ) overlaps day of "Measurement Period" ) or exists ( ["Intervention, Order": "Hospice Care Ambulatory"] HospiceOrder where HospiceOrder.authorDatetime during day of "Measurement Period" ) or exists ( ["Intervention, Performed": "Hospice Care Ambulatory"] HospicePerformed where Global."NormalizeInterval" ( HospicePerformed.relevantDatetime, HospicePerformed.relevantPeriod ) overlaps day of "Measurement Period" ) or exists ( ["Diagnosis": "Hospice Diagnosis"] HospiceCareDiagnosis where HospiceCareDiagnosis.prevalencePeriod overlaps day of "Measurement Period" )
( ["Diagnosis": "Familial Hypercholesterolemia"] Hypercholesterolemia where Hypercholesterolemia.prevalencePeriod starts on or before day of end of "Measurement Period" )
exists "ASCVD Diagnosis or Procedure before End of Measurement Period" and exists "Qualifying Encounter during Day of Measurement Period"
"Patients Age 20 to 75 with LDL Cholesterol Result Greater than or Equal to 190 or Hypercholesterolemia without ASCVD" and exists "Qualifying Encounter during Day of Measurement Period"
"Patients Age 40 to 75 Years with Diabetes without ASCVD or LDL Greater than 190 or Hypercholesterolemia" and exists "Qualifying Encounter during Day of Measurement Period"
"Patients Age 40 to 75 Years and have a 10 Year CVD Risk of High without ASCVD and High LDL and Diabetes" and exists "Qualifying Encounter during Day of Measurement Period"
["Laboratory Test, Performed": "LDL Cholesterol"] LDL190 where LDL190.result >= 190 'mg/dL' and Global."NormalizeInterval" ( LDL190.relevantDatetime, LDL190.relevantPeriod ) starts on or before day of end of "Measurement Period"
( ["Medication, Active": "Low Intensity Statin Therapy"] union ["Medication, Active": "Moderate Intensity Statin Therapy"] union ["Medication, Active": "High Intensity Statin Therapy"] ) ActiveStatin where Global."NormalizeInterval" ( ActiveStatin.relevantDatetime, ActiveStatin.relevantPeriod ) overlaps day of "Measurement Period"
exists "Statin Therapy Ordered during Measurement Period" or exists "Medication Active during the Measurement Period"
exists ( ["Assessment, Performed": "Functional Assessment of Chronic Illness Therapy - Palliative Care Questionnaire (FACIT-Pal)"] PalliativeAssessment where Global."NormalizeInterval" ( PalliativeAssessment.relevantDatetime, PalliativeAssessment.relevantPeriod ) overlaps day of "Measurement Period" ) or exists ( ["Diagnosis": "Palliative Care Diagnosis"] PalliativeDiagnosis where PalliativeDiagnosis.prevalencePeriod overlaps day of "Measurement Period" ) or exists ( ["Encounter, Performed": "Palliative Care Encounter"] PalliativeEncounter where PalliativeEncounter.relevantPeriod overlaps day of "Measurement Period" ) or exists ( ["Intervention, Performed": "Palliative Care Intervention"] PalliativeIntervention where Global."NormalizeInterval" ( PalliativeIntervention.relevantDatetime, PalliativeIntervention.relevantPeriod ) overlaps day of "Measurement Period" )
"Patients Aged 20 to 75 at Start of Measurement Period" and exists ( "LDL Result Greater Than or Equal To 190" union "Hypercholesterolemia Diagnosis" ) and not exists "ASCVD Diagnosis or Procedure before End of Measurement Period"
AgeInYearsAt(date from start of "Measurement Period") in Interval[40, 75] and "Ten Year CVD Risk is High" and not ( exists "ASCVD Diagnosis or Procedure before End of Measurement Period" or exists "Hypercholesterolemia Diagnosis" or exists "LDL Result Greater Than or Equal To 190" or "Has Diabetes Diagnosis" )
AgeInYearsAt(date from start of "Measurement Period") in Interval[40, 75] and "Has Diabetes Diagnosis" and ( not exists "ASCVD Diagnosis or Procedure before End of Measurement Period" and not exists "LDL Result Greater Than or Equal To 190" and not exists "Hypercholesterolemia Diagnosis" )
AgeInYearsAt(date from start of "Measurement Period") in Interval[20, 75]
( ["Encounter, Performed": "Annual Wellness Visit"] union ["Encounter, Performed": "Office Visit"] union ["Encounter, Performed": "Outpatient Consultation"] union ["Encounter, Performed": "Outpatient Encounters for Preventive Care"] union ["Encounter, Performed": "Preventive Care Services Established Office Visit, 18 and Up"] union ["Encounter, Performed": "Unlisted preventive medicine service"] union ["Encounter, Performed": "Preventive Care Services Individual Counseling"] union ["Encounter, Performed": "Preventive Care Services Initial Office Visit, 18 and Up"] ) ValidEncounter where ValidEncounter.relevantPeriod during day of "Measurement Period"
["Patient Characteristic Ethnicity": "Ethnicity"]
["Patient Characteristic Payer": "Payer Type"]
["Patient Characteristic Race": "Race"]
["Patient Characteristic Sex": "ONC Administrative Sex"]
( ["Medication, Order": "Low Intensity Statin Therapy"] union ["Medication, Order": "Moderate Intensity Statin Therapy"] union ["Medication, Order": "High Intensity Statin Therapy"] ) StatinOrdered where StatinOrdered.authorDatetime during day of "Measurement Period"
( exists ( ["Assessment, Performed": "Cardiovascular disease 10Y risk [Likelihood]"] union ["Assessment, Performed": "Cardiovascular disease 10Y risk [Likelihood] ACC-AHA Pooled Cohort by Goff 2013"] ) AtRiskCVD where AtRiskCVD.result as Quantity >= 20 '%' and Global."NormalizeInterval" ( AtRiskCVD.relevantDatetime, AtRiskCVD.relevantPeriod ) during day of "Measurement Period" )
if pointInTime is not null then Interval[pointInTime, pointInTime] else if period is not null then period else null as Interval<DateTime>
["Patient Characteristic Ethnicity": "Ethnicity"]
["Patient Characteristic Payer": "Payer Type"]
["Patient Characteristic Race": "Race"]
["Patient Characteristic Sex": "ONC Administrative Sex"]
Measure Set |
None |
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