Patterns and Impact of Dual Antiplatelet Cessation on Cardiovascular Risk After Percutaneous Coronary Intervention in Patients With Acute Coronary Syndromes.
Acute Coronary Syndrome
/ diagnosis
Drug Administration Schedule
Drug Therapy, Combination
Female
Follow-Up Studies
Humans
Male
Middle Aged
Percutaneous Coronary Intervention
Platelet Aggregation Inhibitors
/ administration & dosage
Postoperative Period
Prognosis
Prospective Studies
Risk Factors
Withholding Treatment
Journal
The American journal of cardiology
ISSN: 1879-1913
Titre abrégé: Am J Cardiol
Pays: United States
ID NLM: 0207277
Informations de publication
Date de publication:
01 03 2019
01 03 2019
Historique:
received:
29
10
2018
revised:
21
11
2018
accepted:
26
11
2018
pubmed:
8
1
2019
medline:
18
12
2019
entrez:
8
1
2019
Statut:
ppublish
Résumé
The aim of this study was to examine the patterns and clinical impact of differing modes of dual-antiplatelet therapy (DAPT) cessation after percutaneous coronary intervention (PCI) in patients presenting with and without acute coronary syndromes (ACS). The PARIS (patterns of nonadherence to antiplatelet regimens in stented patients) registry was a multicenter study of 5,018 patients who underwent PCI. DAPT cessation was categorized as physician-recommended discontinuation, interruption, or disruption. Overall rates of 2-year DAPT discontinuation did not differ between non-ACS and ACS patients (38.8% vs 37.2%, p = 0.252). ACS patients were less likely to interrupt DAPT (8.5% vs 10.7% p<0.001), but were more likely to disrupt DAPT (16.4% vs 11.9%, p<0001). Adverse events after DAPT cessation were highest after disruption, intermediate with discontinuation, and lowest with interruption across both groups. Disruption of DAPT predicted MACE in both ACS patients (hazard ratio [HR] 2.89 [1.88 to 4.45; p<0.001]) and non-ACS patients (HR 2.08 [1.29 to 3.35; p = 0.002]). Interruption of DAPT predicated MACE in ACS patients (HR 2.72 [1.35 to 5.48]) but not in non-ACS patients (HR 0.44 [0.14 to 1.40]; p
Identifiants
pubmed: 30612724
pii: S0002-9149(18)32156-8
doi: 10.1016/j.amjcard.2018.11.051
pii:
doi:
Substances chimiques
Platelet Aggregation Inhibitors
0
Types de publication
Journal Article
Multicenter Study
Observational Study
Langues
eng
Sous-ensembles de citation
IM
Pagination
709-716Informations de copyright
Copyright © 2018. Published by Elsevier Inc.