Safety and efficacy of antiplatelet regimens after percutaneous coronary intervention using drug eluting stents: A network meta-analysis of randomized controlled trials.


Journal

Progress in cardiovascular diseases
ISSN: 1873-1740
Titre abrégé: Prog Cardiovasc Dis
Pays: United States
ID NLM: 0376442

Informations de publication

Date de publication:
Historique:
received: 29 03 2020
accepted: 29 03 2020
pubmed: 6 4 2020
medline: 18 8 2020
entrez: 6 4 2020
Statut: ppublish

Résumé

We aimed to determine the efficacy and safety of different anti-platelet regimens after percutaneous coronary intervention (PCI) with drug eluting stent (DES) implantation using a network meta-analysis of randomized controlled trials (RCTs). RCTs comparing shorter duration (≤6 months) of dual antiplatelet therapy (S-DAPT) with either aspirin (ASA) or P2Y12 inhibitor monotherapy against longer duration (≥12 months) DAPT (L-DAPT) after PCI were searched in the MEDLINE, EMBASE and COCHRANE databases. End-points of interest were all-cause death, cardiovascular (CV) death, myocardial infarction (MI), stent thrombosis (ST), major bleeding and major or minor bleeding. Network meta-analyses were performed using frequentist approach. Eighteen RCTs with total of 57,942 patients met the inclusion and exclusion criteria. This included 14 RCTs (N = 28,853) of S-DAPT with ASA monotherapy and 4 RCTs (N = 29,089) with P2Y12 inhibitor monotherapy. Compared with L-DAPT, the odds of MI were higher with S-DAPT with ASA monotherapy [OR 1.23; 95% CI 1.01-1.48], but not with P2Y12 inhibitor monotherapy [0.98; 0.85-1.14]. Both S-DAPT regimens lowered rates of major bleeding when compared with L-DAPT; ASA monotherapy [0.70; 0.49-1.00] and P2Y12 monotherapy [0.67; 0.45-0.98]. There were no differences in risks of all-cause or CV death between either regimen of S-DAPT and L-DAPT. However, in the acute coronary syndrome subgroup, ASA monotherapy was associated with increased risk of ST [1.55; 1.021-2.36] but P2Y12 monotherapy was not [0.93; 0.58-1.48]. Amongst patients undergoing DES implantation, S-DAPT with P2Y12 inhibitor monotherapy reduces bleeding without increased risk of MI or ST compared with L-DAPT. Prospective trials are needed to evaluate if S-DAPT with P2Y12 monotherapy is superior to S-DAPT with ASA monotherapy for ischemic protection.

Identifiants

pubmed: 32247786
pii: S0033-0620(20)30072-4
doi: 10.1016/j.pcad.2020.03.018
pii:
doi:

Substances chimiques

Platelet Aggregation Inhibitors 0

Types de publication

Journal Article Meta-Analysis Systematic Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

243-248

Informations de copyright

Copyright © 2020 Elsevier Inc. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of competing interest None declared.

Auteurs

Aakash Garg (A)

Division of Cardiology, Newark Beth Israel Medical Center, NJ, USA; Cardiovascular Institute, Rutgers Robert Wood Johnson Medical School, NJ, USA.

Amit Rout (A)

Department of Medicine, Sinai Hospital, Baltimore, MD, USA.

Abhishek Sharma (A)

Section of Cardiovascular Medicine, Gundersen Health System, WI, USA. Electronic address: abhisheksharma4mamc@gmail.com.

Davit Sargsyan (D)

Cardiovascular Institute, Rutgers Robert Wood Johnson Medical School, NJ, USA.

Traymon Beavers (T)

Cardiovascular Institute, Rutgers Robert Wood Johnson Medical School, NJ, USA.

Udaya Tantry (U)

Department of Medicine, Sinai Hospital, Baltimore, MD, USA.

Paul Gurbel (P)

Department of Medicine, Sinai Hospital, Baltimore, MD, USA.

Sunil V Rao (SV)

Duke Clinical Research Institute, Durham, NC, USA.

John B Kostis (JB)

Cardiovascular Institute, Rutgers Robert Wood Johnson Medical School, NJ, USA.

Marc Cohen (M)

Division of Cardiology, Newark Beth Israel Medical Center, NJ, USA.

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH