Control of Low-Density Lipoprotein Cholesterol in Secondary Prevention of Coronary Artery Disease in Real-Life Practice: The DAUSSET Study in French Cardiologists
- PMID: 34945235
- PMCID: PMC8707804
- DOI: 10.3390/jcm10245938
Control of Low-Density Lipoprotein Cholesterol in Secondary Prevention of Coronary Artery Disease in Real-Life Practice: The DAUSSET Study in French Cardiologists
Abstract
Introduction: Patients with established coronary artery disease (CAD) are at very high risk for cardiovascular events.
Methods: The DAUSSET study is a national, multicenter, non-interventional study that included very high-risk CAD patients followed by French cardiologists. It aimed to describe real-life clinical practices for low-density lipoprotein (LDL) cholesterol control in the secondary prevention of CAD.
Results: A total of 912 patients (mean age, 65.4 years; men, 76.1%; myocardial infarction, 69.4%; first episode, 80.1%) were analyzed. The LDL cholesterol goal was 70 mg/dL in most cases (84.9%). The LDL cholesterol goal <70 mg/dL was achieved in 41.7% of patients. Of the 894 (98.0%) patients who received lipid-lowering therapy, 81.2% had been treated more intensively after the cardiac event, 27.0% had been treated less intensively and 13.1% had been maintained. Participating cardiologists were very satisfied or satisfied with treatment response in 72.6% of patients. Moderate satisfaction or dissatisfaction with lipid-lowering therapy was related to not achieving objectives (100%), treatment inefficacy (53.7%), treatment intolerance (23.4%) and poor adherence (12.3%).
Conclusion: These real-world results show that lipid control in very high-risk patients remains insufficient. More than half of the patients did not achieve the LDL cholesterol goal. Prevention of cardiovascular events in these very high-risk patients could be further improved by better education and more intensive lipid-lowering therapy.
Keywords: coronary artery disease; dyslipidemia; guidelines adherence; hypercholesterolemia; myocardial infarction; secondary prevention.
Conflict of interest statement
J. Ferrières has received consulting fees from Amgen, Akcea, Boehringer, Sanofi and Servier. F. Roubille has received consulting fees from Abbott, Air Liquide, Amgen, AstraZeneca, Bayer, Boehringer, Medtronic, Novonordisk, Pfizer, Sanofi, Servier and Zoll, and research grants from AstraZeneca. M. Farnier has received consulting fees from Abbott, Amarin, Amgen, AstraZeneca, Austell, Merck, Mylan, Pfizer, Sanofi and Servier. P. Jourdain has nothing to declare. D. Angoulvant has received consulting fees from Amgen, Alnylam, Astra Zeneca, Bayer, Boehringer, BMS, Novartis, Novo Nordisk, Pfizer, Sanofi and Servier. F. Boccara has received consulting fees from Amgen, Gilead, MSD, Sanofi, Servier and ViiV Healthcare. N. Danchin reports having received grants, speaking fees, consulting fees or non-financial support from Amgen, AstraZeneca, Bayer, BMS, Boehringer-Ingelheim, Intercept, MSD, Novo-Nordisk, Pfizer, Sanofi, Servier, UCB and Vifor.
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