Optimal duration and combination of antiplatelet therapies following percutaneous coronary intervention: a meta-analysis.


Journal

Vascular pharmacology
ISSN: 1879-3649
Titre abrégé: Vascul Pharmacol
Pays: United States
ID NLM: 101130615

Informations de publication

Date de publication:
06 2021
Historique:
received: 25 11 2020
revised: 22 12 2020
accepted: 17 03 2021
pubmed: 24 3 2021
medline: 27 11 2021
entrez: 23 3 2021
Statut: ppublish

Résumé

The ideal duration of dual antiplatelet therapy (DAPT) following percutaneous coronary intervention (PCI) is still unknown. In this meta-analysis, we aimed to compare very short-term (1-3 months), short-term (6 months), standard-term (12 months) and long-term (>12 months) DAPT durations for efficacy and safety. Overall DAPT comparisons were classified as "any shorter-term"/"any longer-term" DAPT. The primary outcome was a composite of major adverse cardiovascular events (MACE: non-fatal myocardial infarction, non-fatal stroke and cardiovascular death). The primary safety outcome was major bleeding. Twenty-six studies comprising 103.394 patients were included. Compared with standard-term DAPT duration, very short-term DAPT duration with subsequent drop of aspirin (RR 1.06, 95% CI, 0.95-1.18, p = 0.26) or drop of the P2Y DAPT may be shortened to 1-3 months in patients with low ischemic but high bleeding risk followed by aspirin or P2Y CRD42020163719.

Identifiants

pubmed: 33753284
pii: S1537-1891(21)00030-6
doi: 10.1016/j.vph.2021.106858
pii:
doi:

Substances chimiques

Platelet Aggregation Inhibitors 0

Types de publication

Journal Article Meta-Analysis Research Support, Non-U.S. Gov't Systematic Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

106858

Informations de copyright

Copyright © 2021 The Authors. Published by Elsevier Inc. All rights reserved.

Auteurs

Georg Gelbenegger (G)

Department of Clinical Pharmacology, Medical University of Vienna, Vienna, Austria.

Ummahan Erari-Canyurt (U)

Department of Internal Medicine II, Division of Cardiology, Medical University of Vienna, Vienna, Austria.

Jürgen Grafeneder (J)

Department of Emergency Medicine, Medical University of Vienna, Vienna, Austria.

Bernd Jilma (B)

Department of Clinical Pharmacology, Medical University of Vienna, Vienna, Austria.

Maciej Lesiak (M)

1st Department of Cardiology, Poznan University of Medical Sciences, Poznan, Poland.

Anna Komosa (A)

1st Department of Cardiology, Poznan University of Medical Sciences, Poznan, Poland.

Raffaele de Caterina (R)

University of Pisa, Pisa, Italy; Fondazione Villa Serena per la Ricerca, Città S. Angelo, Pescara, Italy.

Marek Postula (M)

Department of Experimental and Clinical Pharmacology, Centre for Preclinical Research and Technology (CEPT), Medical University of Warsaw, Warsaw, Poland.

Jolanta M Siller-Matula (JM)

Department of Internal Medicine II, Division of Cardiology, Medical University of Vienna, Vienna, Austria; Department of Experimental and Clinical Pharmacology, Centre for Preclinical Research and Technology (CEPT), Medical University of Warsaw, Warsaw, Poland. Electronic address: Jolanta.siller-matula@meduniwien.ac.at.

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