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  3. Ticagrelor Monotherapy or Dual Antiplatelet Therapy After Drug-Eluting Stent Implantation: Per-Protocol Analysis of the GLOBAL LEADERS Trial.
 

Ticagrelor Monotherapy or Dual Antiplatelet Therapy After Drug-Eluting Stent Implantation: Per-Protocol Analysis of the GLOBAL LEADERS Trial.

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BORIS DOI
10.48350/166332
Date of Publication
May 17, 2022
Publication Type
Article
Division/Institute

Institut für Sozial- ...

Clinical Trials Unit ...

Universitätsklinik fü...

Contributor
Gragnano, Felice
Zwahlen, Marcelorcid-logo
Institut für Sozial- und Präventivmedizin (ISPM)
Vranckx, Pascal
Heg, Dierik Hansorcid-logo
Clinical Trials Unit Bern (CTU)
Schmidlin, Kurt
Institut für Sozial- und Präventivmedizin (ISPM)
Hamm, Christian
Steg, Philippe Gabriel
Gargiulo, Giuseppe
McFadden, Eugene P
Onuma, Yoshinobu
Chichareon, Ply
Benit, Edouard
Möllmann, Helge
Janssens, Luc
Leonardi, Sergio
Zurakowski, Aleksander
Arrivi, Alessio
Van Geuns, Robert Jan
Huber, Kurt
Slagboom, Ton
Calabrò, Paolo
Serruys, Patrick W
Jüni, Peter
Valgimigli, Marco
Windecker, Stephan
Universitätsklinik für Kardiologie
Subject(s)

600 - Technology::610...

300 - Social sciences...

Series
Journal of the American Heart Association
ISSN or ISBN (if monograph)
2047-9980
Publisher
American Heart Association
Language
English
Publisher DOI
10.1161/JAHA.121.024291
PubMed ID
35229616
Uncontrolled Keywords

DAPT P2Y12 inhibitor ...

Description
Background In the GLOBAL LEADERS trial, ticagrelor monotherapy beyond 1 month compared with standard antiplatelet regimens after coronary stent implantation did not improve outcomes at intention-to-treat analysis. Considerable differences in treatment adherence between the experimental and control groups may have affected the intention-to-treat results. In this reanalysis of the GLOBAL LEADERS trial, we compared the experimental and control treatment strategies in a per-protocol analysis of patients who did not deviate from the study protocol. Methods and Results Baseline and postrandomization information were used to classify whether and when patients were deviating from the study protocol. With logistic regressions, we derived time-varying inverse probabilities of nondeviation from protocol to reconstruct the trial population without protocol deviation. The primary end point was a composite of all-cause mortality or nonfatal Q-wave myocardial infarction at 2 years. At 2-year follow-up, 1103 (13.8%) of 7980 patients in the experimental group and 785 (9.8%) of 7988 patients in the control group qualified as protocol deviators. At per-protocol analysis, the rate ratio for the primary end point was 0.88 (95% CI, 0.75-1.03; P=0.10) on the basis of 274 versus 325 events in the experimental versus control group. The rate ratio for the key safety end point of major bleeding was 1.00 (95% CI, 0.79-1.26; P=0.99). The per-protocol and intention-to-treat effect estimates were overall consistent. Conclusions Among patients who complied with the study protocol in the GLOBAL LEADERS trial, ticagrelor plus aspirin for 1 month followed by ticagrelor monotherapy was not superior to 1-year standard dual antiplatelet therapy followed by aspirin alone at 2 years after coronary stenting. Registration URL: https://www.clinicaltrials.gov; Unique identifier: NCT01813435.
Handle
https://boris-portal.unibe.ch/handle/20.500.12422/68029
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Gragnano_JAmHeartAssoc_2022.pdftextAdobe PDF1.59 MBpublishedOpen
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