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Safety and Efficacy of Ticagrelor Monotherapy in Patients with Acute Coronary Syndromes Undergoing Percutaneous Coronary Intervention: An Individual Patient Data Meta-Analysis of TWILIGHT and TICO Randomized Trials

Authors
 Usman Baber  ;  Yangsoo Jang  ;  Angelo Oliva  ;  Davide Cao  ;  Birgit Vogel  ;  George Dangas  ;  Samantha Sartori  ;  Alessandro Spirito  ;  Kenneth F Smith  ;  Mattia Branca  ;  Timothy Collier  ;  Stuart Pocock  ;  Marco Valgimigli  ;  Byeong-Keuk Kim  ;  Myeong-Ki Hong  ;  Roxana Mehran 
Citation
 CIRCULATION, Vol.149(8) : 574-584, 2024-02 
Journal Title
CIRCULATION
ISSN
 0009-7322 
Issue Date
2024-02
MeSH
Acute Coronary Syndrome* / diagnosis ; Acute Coronary Syndrome* / drug therapy ; Acute Coronary Syndrome* / surgery ; Aspirin / adverse effects ; Biomarkers ; Drug Therapy, Combination ; Female ; Hemorrhage / epidemiology ; Humans ; Male ; Middle Aged ; Myocardial Infarction* / therapy ; Percutaneous Coronary Intervention* / adverse effects ; Platelet Aggregation Inhibitors / adverse effects ; Randomized Controlled Trials as Topic ; Stroke* / epidemiology ; Ticagrelor / adverse effects ; Treatment Outcome
Keywords
acute coronary syndrome ; hemorrhage ; percutaneous coronary intervention ; purinergic P2Y receptor antagonists ; ticagrelor
Abstract
Background: Dual antiplatelet therapy with a potent P2Y12 inhibitor coupled with aspirin for 1 year is the recommended treatment for patients with acute coronary syndrome (ACS) undergoing percutaneous coronary intervention (PCI). As an alternative, monotherapy with a P2Y12 inhibitor after a short period of dual antiplatelet therapy has emerged as a bleeding reduction strategy.

Methods: We pooled individual patient data from randomized trials that included patients with ACS undergoing PCI treated with an initial 3-month course of dual antiplatelet therapy followed by ticagrelor monotherapy versus continued ticagrelor plus aspirin. Patients sustaining a major ischemic or bleeding event in the first 3 months after PCI were excluded from analysis. The primary outcome was Bleeding Academic Research Consortium type 3 or 5 bleeding occurring between 3 and 12 months after index PCI. The key secondary end point was the composite of death, myocardial infarction, or stroke. Hazard ratios and 95% CIs were generated using Cox regression with a one-stage approach in the intention-to-treat population.

Results: The pooled cohort (n=7529) had a mean age of 62.8 years, 23.2% were female, and 55% presented with biomarker-positive ACS. Between 3 and 12 months, ticagrelor monotherapy significantly reduced Bleeding Academic Research Consortium 3 or 5 bleeding compared with ticagrelor plus aspirin (0.8% versus 2.1%; hazard ratio, 0.37 [95% CI, 0.24-0.56]; P<0.001). Rates of all-cause death, myocardial infarction, or stroke were not significantly different between groups (2.4% versus 2.7%; hazard ratio, 0.91 [95% CI, 0.68-1.21]; P=0.515). Findings were unchanged among patients presenting with biomarker-positive ACS.

Conclusions: Among patients with ACS undergoing PCI who have completed a 3-month course of dual antiplatelet therapy, discontinuation of aspirin followed by ticagrelor monotherapy significantly reduced major bleeding without incremental ischemic risk compared with ticagrelor plus aspirin.

Registration: URL: https://www.crd.york.ac.uk/prospero; Unique identifier: CRD42023449646.
Full Text
https://www.ahajournals.org/doi/10.1161/CIRCULATIONAHA.123.067283
DOI
10.1161/CIRCULATIONAHA.123.067283
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Internal Medicine (내과학교실) > 1. Journal Papers
Yonsei Authors
Kim, Byeong Keuk(김병극) ORCID logo https://orcid.org/0000-0003-2493-066X
Hong, Myeong Ki(홍명기) ORCID logo https://orcid.org/0000-0002-2090-2031
URI
https://ir.ymlib.yonsei.ac.kr/handle/22282913/201912
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