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  3. Eligibility for PCSK9 Inhibitors According to American College of Cardiology (ACC) and European Society of Cardiology/European Atherosclerosis Society (ESC/EAS) Guidelines After Acute Coronary Syndromes.
 

Eligibility for PCSK9 Inhibitors According to American College of Cardiology (ACC) and European Society of Cardiology/European Atherosclerosis Society (ESC/EAS) Guidelines After Acute Coronary Syndromes.

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BORIS DOI
10.7892/boris.107400
Date of Publication
November 9, 2017
Publication Type
Article
Division/Institute

Universitätsklinik fü...

Berner Institut für H...

Clinical Trials Unit ...

Contributor
Gencer, Baris
Koskinas, Konstantinos
Universitätsklinik für Kardiologie
Räber, Lorenz
Universitätsklinik für Kardiologie
Karagiannis Voules, Alexios
Clinical Trials Unit Bern (CTU)
Institut für Sozial- und Präventivmedizin (ISPM)
Nanchen, David
Auer, Reto
Berner Institut für Hausarztmedizin (BIHAM)
Carballo, David
Carballo, Sebastian
Klingenberg, Roland
Heg, Dierik Hansorcid-logo
Clinical Trials Unit Bern (CTU)
Institut für Sozial- und Präventivmedizin (ISPM)
Matter, Christian M
Lüscher, Thomas F
Rodondi, Nicolas
Berner Institut für Hausarztmedizin (BIHAM)
Clinic of General Internal Medicine
Mach, François
Windecker, Stephan
Universitätsklinik für Kardiologie
Subject(s)

600 - Technology::610...

300 - Social sciences...

Series
Journal of the American Heart Association
ISSN or ISBN (if monograph)
2047-9980
Publisher
American Heart Association
Language
English
Publisher DOI
10.1161/JAHA.117.006537
PubMed ID
29122809
Uncontrolled Keywords

PCSK9 lipids secondar...

Description
BACKGROUND

The American College of Cardiology (ACC) and European Society of Cardiology/European Atherosclerosis Society (ESC/EAS) have recently published recommendations for the use of proprotein convertase subtilisin/kexin-9 (PCSK9) inhibitors in situations of very high risk. We aim to assess in the real world the suitability of PCSK9 inhibitors for acute coronary syndromes.

METHODS AND RESULTS

We analyzed a prospective Swiss cohort of 2023 patients hospitalized for acute coronary syndromes between 2009 and 2014 with available data for low-density lipoprotein cholesterol and lipid-lowering therapy at 1 year. Clinical familial hypercholesterolemia was defined using the Dutch Lipid Clinic Network algorithm as unlikely, possible, probable, or definite. We simulated a fixed relative reduction of 24% in low-density lipoprotein cholesterol levels at 1 year in all patients not treated with ezetimibe, irrespective of the low-density lipoprotein cholesterol levels and statin regimen. At 1 year, 94.3% of patients were treated with statin, 5.8% with ezetimibe, and 35.8% of patients had on-target low-density lipoprotein cholesterol levels (<1.8 mmol/L); 25.6% met criteria for possible or probable/definite familial hypercholesterolemia. After a simulation of the lipid-lowering effect of ezetimibe, the proportion of patients who would be eligible for PCSK9 inhibitors at 1 year was 13.4% using American College of Cardiology criteria and 2.7% using European Society of Cardiology/European Atherosclerosis Society criteria. Patients with possible or probable/definite familial hypercholesterolemia were more eligible for PCSK9 inhibitors compared with their non-familial hypercholesterolemia counterparts: 27.6% versus 8.8% according to American College of Cardiology criteria and 6.6% versus 1.8% according to European Society of Cardiology/European Atherosclerosis Society criteria (P<0.001).

CONCLUSIONS

Recommendations made by the American College of Cardiology guidelines would lead to 5-fold higher eligibility rates for PCSK9 inhibitors compared to the European Society of Cardiology/European Atherosclerosis Society consensus statement in acute coronary syndrome patients.
Handle
https://boris-portal.unibe.ch/handle/20.500.12422/155801
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FileFile TypeFormatSizeLicensePublisher/Copright statementContent
Gencer JAmHeartAssoc 2017.pdftextAdobe PDF1.18 MBAttribution-NonCommercial (CC BY-NC 4.0)publishedOpen
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