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Revision as of 14:46, 28 October 2016
Template:Hypercholesterolemia Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]
Summary of Key Recommendations for the Treatment of Blood Cholesterol to Reduce ASCVD Risk in Adults[1]
A. Heart-healthy lifestyle habits should be encouraged for all individuals
B. The appropriate intensity of statin therapy should be initiated or continued
Class I |
"1.Clinical ASCVD*
|
"2.Primary prevention – Primary LDL-C ‡190 mg/dL
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"3.Primary prevention - Diabetes 40–75 years of age and LDL-C 70–189 mg/dL
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"4. Primary prevention – No diabetes 40–75 years of age and LDL-C 70–189 mg/dL
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Class IIa |
"1.Primary prevention – Primary LDL-C ‡190 mg/dL
|
"2. Primary prevention - Diabetes 40–75 years of age and LDL-C 70–189 mg/dL
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"3. Primary prevention – No diabetes 40–75 years of age and LDL-C 70–189 mg/dL
|
Class IIb |
"1.Primary prevention – Primary LDL-C ‡190 mg/dL
|
"2.Primary prevention – No diabetes 40–75 years of age and LDL-C 70–189 mg/dL
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"3.Primary prevention when LDL-C <190 mg/dL and age <40 or >75 y, or <5% 10-y ASCVD risk
|
Class III |
"1.Statin therapy is not routinely recommended for individuals with NYHA class II-IV heart failure or who are receiving maintenance hemodialysis " |
C. Regularly monitor adherence to lifestyle and drug therapy with lipid and safety assessments
Class I |
"1.Assess adherence, response to therapy, and adverse effects within 4–12 wk following statin initiation or change in therapy
|
Class IIa |
"1.Assess adherence, response to therapy, and adverse effects within 4–12 wk following statin initiation or change in therapy
|
Class IIb |
"1.Assess adherence, response to therapy, and adverse effects within 4–12 wk following statin initiation or change in therapy
|
D. In individuals intolerant of the recommended intensity of statin therapy, use the maximally tolerated intensity of statin
Class I |
"1. If there are muscle or other symptoms, establish that they are related to the statin (Level of Evidence: A) " |
Class IIa |
"1.For specific recommendations on managing muscle symptoms please click here (Level of Evidence: B)" |
*Clinical ASCVD includes acute coronary syndromes, history of MI, stable or unstable angina, coronary or other arterial revascularization, stroke, TIA, or peripheral arterial disease presumed to be of atherosclerotic origin.
†Estimated 10-year or “hard” ASCVD risk includes first occurrence of nonfatal MI, CHD death, and nonfatal and fatal stroke as used by the Risk Assessment Work Group in developing the Pooled Cohort Equations.
‡These factors may include primary LDL-C !160 mg/dL or other evidence of genetic hyperlipidemias; family history of premature ASCVD with onset <55 years of age in a first-degree male relative or <65 years of age in a first-degree female relative; hs-CRP ≥2 mg/L; CAC score ≥300 Agatston units or ≥75th percentile for age, sex, and ethnicity (for additional information, see http://www.mesa-nhlbi.org/ CACReference.aspx); ABI <0.9; or lifetime risk of ASCVD. Additional factors that might aid in individual risk assessment could be identified in the future.
∞High-risk individuals include those with clinical ASCVD, an untreated LDL-C !190 mg/dL suggesting genetic hypercholesterolemia, or individuals with diabetes 40 to 75 years of age and LDL-C 70 to 189 mg/dL.
References
- ↑ 2013 ACC/AHA Guideline on the Treatment of Blood Cholesterol to Reduce Atherosclerotic Cardiovascular Risk in Adults. http://ac.els-cdn.com/S0735109713060282/1-s2.0-S0735109713060282-main.pdf?_tid=06f509a0-9c67-11e6-b670-00000aab0f01&acdnat=1477587879_04fcb2e98e9d9b3a556253eefd0247d2 Accessed on October 27, 2016