TY - JOUR
T1 - Comprehensive comparative efficacy and safety of potent P2Y12 inhibitors in patients undergoing coronary intervention: A systematic review and meta-analysis
AU - Huang, Chien-Lung
AU - Tsao, Ting-Ping
AU - Yin, Wei-Hsian
AU - Huang, Wen-Bin
AU - Huang , Hsu-Lung
AU - Lin, Chang-Chyi
AU - Chang , Chung-Yi
AU - Hsu, Ching-Hwa
N1 - © 2024 The Author(s).
PY - 2024/4
Y1 - 2024/4
N2 - Potent P2Y
12 receptor antagonists have been used widely for patients undergoing percutaneous coronary intervention with different results. Benefits from different regimens various between trials. Randomized controlled trials (RCTs) have restrictive inclusion and exclusion criteria; thus, they may limit the generalizability of the findings to a broader population. This study was aimed to comprehensively investigate the outcomes of potent P2Y
12 inhibitors in patients undergoing PCI, including RCTs and real-world evidence (RWE) studies. Multiple electronic databases were systemically reviewed and searched on compared potent P2Y
12 inhibitors with clopidogrel. The primary efficacy end point was composite ischemic cardiovascular event and primary safety endpoint was major bleeding. Overall estimates of proportions and incidence rates with 95 % confidence intervals (CI) were calculated using fixed-effects models. Total 24 studies (140,986 patients) underwent coronary intervention were included in this
meta-analysis, including 18 RCTs and 6 large cohort studies with propensity score matching. The potent P2Y
12 inhibitors including cangrelor, prasugrel, and ticagrelor, significantly decreased the risk of composite adverse cardiovascular ischemic events (95 % CI 0.89-0.96,
p < 0.001), but increased major bleeding (95 % CI 1.15-1.33,
p < 0.001) or any bleeding (95 % CI 1.21-1.33,
p < 0.001) compared with Clopidogrel. This
meta-analysis merges RCTs and RWE studies and comprehensively evidences newer potent P2Y
12 inhibitors are significantly more effective than clopidogrel in reduction of composite adverse thrombotic events, but the incidence of major or any bleeding was higher compared with clopidogrel.
AB - Potent P2Y
12 receptor antagonists have been used widely for patients undergoing percutaneous coronary intervention with different results. Benefits from different regimens various between trials. Randomized controlled trials (RCTs) have restrictive inclusion and exclusion criteria; thus, they may limit the generalizability of the findings to a broader population. This study was aimed to comprehensively investigate the outcomes of potent P2Y
12 inhibitors in patients undergoing PCI, including RCTs and real-world evidence (RWE) studies. Multiple electronic databases were systemically reviewed and searched on compared potent P2Y
12 inhibitors with clopidogrel. The primary efficacy end point was composite ischemic cardiovascular event and primary safety endpoint was major bleeding. Overall estimates of proportions and incidence rates with 95 % confidence intervals (CI) were calculated using fixed-effects models. Total 24 studies (140,986 patients) underwent coronary intervention were included in this
meta-analysis, including 18 RCTs and 6 large cohort studies with propensity score matching. The potent P2Y
12 inhibitors including cangrelor, prasugrel, and ticagrelor, significantly decreased the risk of composite adverse cardiovascular ischemic events (95 % CI 0.89-0.96,
p < 0.001), but increased major bleeding (95 % CI 1.15-1.33,
p < 0.001) or any bleeding (95 % CI 1.21-1.33,
p < 0.001) compared with Clopidogrel. This
meta-analysis merges RCTs and RWE studies and comprehensively evidences newer potent P2Y
12 inhibitors are significantly more effective than clopidogrel in reduction of composite adverse thrombotic events, but the incidence of major or any bleeding was higher compared with clopidogrel.
KW - Coronary intervention
KW - Potent P2Y inhibitor
KW - Randomized control trial
KW - Real-world evidence
UR - https://www.scopus.com/pages/publications/85185161181
U2 - 10.1016/j.ijcha.2024.101359
DO - 10.1016/j.ijcha.2024.101359
M3 - Review article
C2 - 38371311
VL - 51
SP - 101359
JO - International Journal of Cardiology Heart and Vasculature
JF - International Journal of Cardiology Heart and Vasculature
M1 - 101359
ER -