Early Aspirin Discontinuation After Coronary Stenting: A Systematic Review and Meta-Analysis.
Aspirin
/ administration & dosage
Coronary Restenosis
/ prevention & control
Dual Anti-Platelet Therapy
/ methods
Duration of Therapy
Hemorrhage
/ chemically induced
Humans
Percutaneous Coronary Intervention
/ adverse effects
Risk Assessment
Stents
Withholding Treatment
/ statistics & numerical data
aspirin
coronary artery disease
meta‐analysis
stent
Journal
Journal of the American Heart Association
ISSN: 2047-9980
Titre abrégé: J Am Heart Assoc
Pays: England
ID NLM: 101580524
Informations de publication
Date de publication:
19 01 2021
19 01 2021
Historique:
pubmed:
8
1
2021
medline:
15
10
2021
entrez:
7
1
2021
Statut:
ppublish
Résumé
Background The clinical impact of early aspirin discontinuation compared with dual antiplatelet therapy (DAPT) in patients undergoing percutaneous coronary intervention with stenting remains poorly studied. We investigated the clinical outcomes of patients assigned to either early aspirin discontinuation or DAPT after percutaneous coronary intervention with stenting. Methods and Results We performed a meta-analysis of aggregate data from randomized clinical trials enrolling participants receiving a percutaneous coronary intervention with stenting and assigned to either early aspirin discontinuation or DAPT. Scientific databases were searched from inception through March 30, 2020. Trial-level hazard ratios (HRs) and 95% CIs were pooled using a random effects model with inverse variance weighting. The primary outcome was all-cause death. Secondary outcomes were myocardial infarction, stent thrombosis, stroke, and major bleeding. Overall, 36 206 participants were allocated to either early aspirin discontinuation (experimental therapy, n=18 088) or DAPT (control therapy, n=18 118) in 7 trials. Median follow-up was 12 months. All-cause death occurred in 2.5% of patients assigned to experimental and 2.9% of patients assigned control therapy (hazard ratio [HR], 0.91, 95% CI, 0.75-1.11;
Identifiants
pubmed: 33410332
doi: 10.1161/JAHA.120.018304
pmc: PMC7955304
doi:
Substances chimiques
Aspirin
R16CO5Y76E
Types de publication
Journal Article
Meta-Analysis
Systematic Review
Langues
eng
Sous-ensembles de citation
IM
Pagination
e018304Références
PLoS One. 2013;8(3):e59202
pubmed: 23544056
JAMA. 1999 Sep 15;282(11):1054-60
pubmed: 10493204
N Engl J Med. 2016 Dec 22;375(25):2423-2434
pubmed: 27959713
J Am Heart Assoc. 2021 Jan 19;10(2):e018304
pubmed: 33410332
N Engl J Med. 1996 Apr 25;334(17):1084-9
pubmed: 8598866
BMJ. 2002 Jan 12;324(7329):71-86
pubmed: 11786451
Circulation. 2019 Dec 3;140(23):1921-1932
pubmed: 31557056
N Engl J Med. 2019 Nov 21;381(21):2032-2042
pubmed: 31556978
Ann Intern Med. 2009 Aug 18;151(4):264-9, W64
pubmed: 19622511
JAMA. 2019 Jun 25;321(24):2428-2437
pubmed: 31237645
Lancet. 2019 Oct 12;394(10206):1335-1343
pubmed: 31492505
Nat Rev Cardiol. 2018 Aug;15(8):480-496
pubmed: 29973709
Eur Heart J. 2018 Jan 14;39(3):213-260
pubmed: 28886622
Lancet. 2018 Sep 15;392(10151):940-949
pubmed: 30166073
J Am Coll Cardiol. 1997 Jan;29(1):28-34
pubmed: 8996291
Lancet. 2013 Mar 30;381(9872):1107-15
pubmed: 23415013
BMJ Open. 2016 Jul 12;6(7):e010247
pubmed: 27406637
BMJ. 2011 Oct 18;343:d5928
pubmed: 22008217
N Engl J Med. 2017 Oct 19;377(16):1513-1524
pubmed: 28844193
N Engl J Med. 2019 Apr 18;380(16):1509-1524
pubmed: 30883055
JAMA. 2019 Jun 25;321(24):2414-2427
pubmed: 31237644
JAMA. 2019 Jan 22;321(3):277-287
pubmed: 30667501
Circulation. 2020 Oct 13;142(15):1425-1436
pubmed: 32795096