Abstract | BACKGROUND: METHODS: In this prospective cross-sectional study, patients with ACS between 2009 and 2016 and with available LDL-c at one year were considered. We defined three mutually exclusive groups of patients according to eligibility for PCSK9i: "not eligible", "currently eligible", and "newly eligible". We explored the control of cardiovascular risk factors and health behaviors. RESULTS: Out of 3025 patients who had an ACS one year ago, 1071 (35.4%) were not eligible for PCSK9i, 415 (13.7%) were currently eligible, and 1539 (50.9%) were newly eligible. The proportion of patients with uncontrolled hypertension in the not eligible group was lower than in the group currently eligible (27.6% vs 33.6%, p = 0.02), but similar to the group newly eligible (27.6% vs 28.2%, p = 0.73). The proportion of smokers in the not eligible group was lower than in the group currently eligible (21.2% vs 28.0%, p = 0.02), but similar to the group newly eligible (21.2% vs 22.5%, p = 0.51). CONCLUSIONS: More than half of patients with ACS would be additionally eligible for PCSK9i if prescription is extended from current guidelines to all patients with LDL-c equal or above 1.8 mmol/l. Patients currently eligible for PCSK9i one year after an ACS had a worst control of cardiovascular risk factors than patients potentially newly eligible.
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Authors | Audrey Butty, Baris Gencer, Konstantinos C Koskinas, David Carballo, Lorenz Räber, Roland Klingenberg, Christian M Matter, Thomas F Lüscher, Stephan Windecker, Olivier Muller, Nicolas Rodondi, François Mach, David Nanchen |
Journal | International journal of cardiology
(Int J Cardiol)
Vol. 299
Pg. 289-295
(01 15 2020)
ISSN: 1874-1754 [Electronic] Netherlands |
PMID | 31668506
(Publication Type: Journal Article, Observational Study)
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Copyright | Copyright © 2019 Elsevier B.V. All rights reserved. |
Chemical References |
- Cardiovascular Agents
- Enzyme Inhibitors
- PCSK9 Inhibitors
- PCSK9 protein, human
- Proprotein Convertase 9
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Topics |
- Acute Coronary Syndrome
(drug therapy, enzymology)
- Aged
- Cardiovascular Agents
(administration & dosage)
- Cardiovascular Diseases
(drug therapy, enzymology)
- Cross-Sectional Studies
- Enzyme Inhibitors
(administration & dosage)
- Female
- Health Behavior
(drug effects, physiology)
- Humans
- Male
- Middle Aged
- PCSK9 Inhibitors
- Proprotein Convertase 9
(metabolism)
- Prospective Studies
- Risk Factors
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