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Chronic Coronary Disease 2023

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24 Treatment 4.2.6. Lipid Management COR LOE Recommendations Cost Value Statement: High Value B-NR 6. In patients with CCD, addition of generic ezetimibe to maximally tolerated statin therapy in appropriately selected patients is projected to be of high economic value at US prices. 2a A 7. In patients with CCD who are judged to be at very high risk (Table 10) and who have an LDL-C level ≥70 mg/ dL (≥1.8 mmol/L), or a non–high-density lipoprotein cholesterol (HDL-C) level ≥100 mg/dL (≥2.6 mmol/L), on maximally tolerated statin and ezetimibe, a PCSK9 monoclonal antibody can be beneficial to further reduce the risk of MACE.* Cost Value Statement: Uncertain B-NR 8. In patients with CCD who are very high risk, the use of PCSK9 monoclonal antibodies is projected to be of uncertain economic value at US prices. 2b B-R 9. In patients with CCD on maximally tolerated statin therapy with an LDL-C level <100 mg/dL (<2.6 mmol/L) and a persistent fasting triglyceride level of 150 to 499 mg/ dL (1.7–5.6 mmol/L) after addressing secondary causes, icosapent ethyl may be considered to further reduce the risk of MACE and cardiovascular death. 2b B-R 10. In patients with CCD who are not at very high risk and on maximally tolerated statin therapy with an LDL-C level ≥70 mg/dL (≥1.8 mmol/L), it may be reasonable to add ezetimibe to further reduce the risk of MACE.* 2b B-R 11. In patients with CCD on maximally tolerated statin therapy who have an LDL-C level ≥70 mg/dL (≥1.8 mmol/L), and in whom ezetimibe and PCSK9 monoclonal antibody are deemed insufficient or not tolerated, it may be reasonable to add bempedoic acid or inclisiran (in place of PCSK9 monoclonal antibody) to further reduce LDL-C levels. 3: No Benefit B-R 12. In patients with CCD receiving statin therapy, adding niacin, or fenofibrate or dietary supplements containing omega-3 fatty acids, are not beneficial in reducing cardiovascular risk. * Modified from the 2018 AHA/ACC/Multisociety guideline on the management of blood cholesterol. Grundy SM, et al. J Am Coll Cardiol. 2019;73:e285-e350. (cont'd)

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