TY - JOUR
T1 - P2Y12 Inhibitor or Aspirin Monotherapy for Secondary Prevention of Coronary Events
AU - PANTHER Collaboration
AU - Gragnano, Felice
AU - Cao, Davide
AU - Pirondini, Leah
AU - Franzone, Anna
AU - Kim, Hyo Soo
AU - von Scheidt, Moritz
AU - Pettersen, Alf Åge R.
AU - Zhao, Qiang
AU - Woodward, Mark
AU - Chiarito, Mauro
AU - McFadden, Eugene P.
AU - Park, Kyung Woo
AU - Kastrati, Adnan
AU - Seljeflot, Ingebjørg
AU - Zhu, Yunpeng
AU - Windecker, Stephan
AU - Kang, Jeehoon
AU - Schunkert, Heribert
AU - Arnesen, Harald
AU - Bhatt, Deepak L.
AU - Steg, Philippe Gabriel
AU - Calabrò, Paolo
AU - Pocock, Stuart
AU - Mehran, Roxana
AU - Valgimigli, Marco
N1 - Publisher Copyright:
© 2023 American College of Cardiology Foundation
PY - 2023/7/11
Y1 - 2023/7/11
N2 - Background: Aspirin is the only antiplatelet agent with a Class I recommendation for long-term prevention of cardiovascular events in patients with coronary artery disease (CAD). There is inconsistent evidence on how it compares with alternative antiplatelet agents. Objectives: This study compared P2Y12 inhibitor monotherapy vs aspirin in patients with CAD. Methods: We conducted a patient-level meta-analysis of randomized trials comparing P2Y12 inhibitor monotherapy vs aspirin monotherapy for the prevention of cardiovascular events in patients with established CAD. The primary outcome was the composite of cardiovascular death, myocardial infarction, and stroke. Prespecified key secondary outcomes were major bleeding and net adverse clinical events (the composite of the primary outcome and major bleeding). Data were pooled in a 1-step meta-analysis. Results: Patient-level data were obtained from 7 trials. Overall, 24,325 participants were available for analysis, including 12,178 patients assigned to receive P2Y12 inhibitor monotherapy (clopidogrel in 7,545 [62.0%], ticagrelor in 4,633 [38.0%]) and 12,147 assigned to receive aspirin. Risk of the primary outcome was lower with P2Y12 inhibitor monotherapy compared with aspirin over 2 years (HR: 0.88; 95% CI: 0.79-0.97; P = 0.012), mainly owing to less myocardial infarction (HR: 0.77; 95% CI: 0.66-0.90; P < 0.001). Major bleeding was similar (HR: 0.87; 95% CI: 0.70-1.09; P = 0.23) and net adverse clinical events were lower (HR: 0.89; 95% CI: 0.81-0.98; P = 0.020) with P2Y12 inhibitors. The treatment effect was consistent across prespecified subgroups and types of P2Y12 inhibitors. Conclusions: Given its superior efficacy and similar overall safety, P2Y12 inhibitor monotherapy might be preferred over aspirin monotherapy for long-term secondary prevention in patients with established CAD.
AB - Background: Aspirin is the only antiplatelet agent with a Class I recommendation for long-term prevention of cardiovascular events in patients with coronary artery disease (CAD). There is inconsistent evidence on how it compares with alternative antiplatelet agents. Objectives: This study compared P2Y12 inhibitor monotherapy vs aspirin in patients with CAD. Methods: We conducted a patient-level meta-analysis of randomized trials comparing P2Y12 inhibitor monotherapy vs aspirin monotherapy for the prevention of cardiovascular events in patients with established CAD. The primary outcome was the composite of cardiovascular death, myocardial infarction, and stroke. Prespecified key secondary outcomes were major bleeding and net adverse clinical events (the composite of the primary outcome and major bleeding). Data were pooled in a 1-step meta-analysis. Results: Patient-level data were obtained from 7 trials. Overall, 24,325 participants were available for analysis, including 12,178 patients assigned to receive P2Y12 inhibitor monotherapy (clopidogrel in 7,545 [62.0%], ticagrelor in 4,633 [38.0%]) and 12,147 assigned to receive aspirin. Risk of the primary outcome was lower with P2Y12 inhibitor monotherapy compared with aspirin over 2 years (HR: 0.88; 95% CI: 0.79-0.97; P = 0.012), mainly owing to less myocardial infarction (HR: 0.77; 95% CI: 0.66-0.90; P < 0.001). Major bleeding was similar (HR: 0.87; 95% CI: 0.70-1.09; P = 0.23) and net adverse clinical events were lower (HR: 0.89; 95% CI: 0.81-0.98; P = 0.020) with P2Y12 inhibitors. The treatment effect was consistent across prespecified subgroups and types of P2Y12 inhibitors. Conclusions: Given its superior efficacy and similar overall safety, P2Y12 inhibitor monotherapy might be preferred over aspirin monotherapy for long-term secondary prevention in patients with established CAD.
KW - P2Y inhibitor
KW - aspirin
KW - coronary artery disease
KW - meta-analysis
KW - myocardial infarction
UR - http://www.scopus.com/inward/record.url?scp=85162885269&partnerID=8YFLogxK
U2 - 10.1016/j.jacc.2023.04.051
DO - 10.1016/j.jacc.2023.04.051
M3 - Article
AN - SCOPUS:85162885269
SN - 0735-1097
VL - 82
SP - 89
EP - 105
JO - Journal of the American College of Cardiology
JF - Journal of the American College of Cardiology
IS - 2
ER -