TY - JOUR
T1 - Prasugrel vs Ticagrelor for DAPT in Patients with ACS Undergoing PCI
T2 - A Systematic Review and Meta-Analysis of Randomized Controlled Trials
AU - Al-Abdouh, Ahmad
AU - Barbarawi, Mahmoud
AU - Abusnina, Waiel
AU - Amr, Mahmoud
AU - Zhao, Di
AU - Savji, Nazir
AU - Hasan, Rani K.
AU - Michos, Erin D.
N1 - Publisher Copyright:
© 2020 Elsevier Inc.
PY - 2020/12
Y1 - 2020/12
N2 - Introduction: Dual antiplatelet therapy (DAPT) with a P2Y12 inhibitor added to aspirin is considered the standard of care for patients with acute coronary syndrome (ACS) undergoing percutaneous intervention (PCI). Prasugrel and ticagrelor are commonly used P2Y12 inhibitors, and a few head-to-head randomized control trials (RCTs) have been performed. We performed a systematic review and meta-analysis of these RCTs to compare the efficacy and adverse effects between these two agents when used in patients with ACS undergoing PCI. Methods: We searched PubMed/MEDLINE and Cochrane library for RCTs comparing prasugrel to ticagrelor in ACS. The primary endpoint was major adverse cardiovascular events (MACE). Secondary outcomes were all-cause mortality, cardiovascular mortality, myocardial infarction (MI), stent thrombosis, major bleeding, and all bleeding event. Estimates were calculated as random effects risk ratios (RRs) with 95% confidence intervals (CI). Results: Six trials with 6807 patients were included. There were no significant difference of MACE (RR 0.93; 95% CI [0.72–1.20]; p = 0.59; I2 = 26%), all-cause mortality (RR 0.92; 95% CI [0.73–1.17]; p = 0.51; I2 = 0%), cardiovascular mortality (RR 0.99; 95% CI [0.75–1.31]; p = 0.96; I2 = 0%), MI (RR 0.87; 95% CI [0.60–1.27]; p = 0.48; I2 = 27%), stent thrombosis (RR 0.64; 95% CI [0.39–1.04]; p = 0.07; I2 = 0%), major bleeding (RR 0.94; 95% CI [0.70–1.26]; p = 0.68; I2 = 6%), and all bleeding event (RR 0.92; 95% CI [0.77–1.09]; p = 0.32; I2 = 0%) for prasugrel compared with ticagrelor. Conclusion: There are no significant difference of MACE, all-cause mortality, cardiovascular mortality, MI, stent thrombosis, and bleeding between prasugrel and ticagrelor when added to aspirin among patients with ACS undergoing PCI.
AB - Introduction: Dual antiplatelet therapy (DAPT) with a P2Y12 inhibitor added to aspirin is considered the standard of care for patients with acute coronary syndrome (ACS) undergoing percutaneous intervention (PCI). Prasugrel and ticagrelor are commonly used P2Y12 inhibitors, and a few head-to-head randomized control trials (RCTs) have been performed. We performed a systematic review and meta-analysis of these RCTs to compare the efficacy and adverse effects between these two agents when used in patients with ACS undergoing PCI. Methods: We searched PubMed/MEDLINE and Cochrane library for RCTs comparing prasugrel to ticagrelor in ACS. The primary endpoint was major adverse cardiovascular events (MACE). Secondary outcomes were all-cause mortality, cardiovascular mortality, myocardial infarction (MI), stent thrombosis, major bleeding, and all bleeding event. Estimates were calculated as random effects risk ratios (RRs) with 95% confidence intervals (CI). Results: Six trials with 6807 patients were included. There were no significant difference of MACE (RR 0.93; 95% CI [0.72–1.20]; p = 0.59; I2 = 26%), all-cause mortality (RR 0.92; 95% CI [0.73–1.17]; p = 0.51; I2 = 0%), cardiovascular mortality (RR 0.99; 95% CI [0.75–1.31]; p = 0.96; I2 = 0%), MI (RR 0.87; 95% CI [0.60–1.27]; p = 0.48; I2 = 27%), stent thrombosis (RR 0.64; 95% CI [0.39–1.04]; p = 0.07; I2 = 0%), major bleeding (RR 0.94; 95% CI [0.70–1.26]; p = 0.68; I2 = 6%), and all bleeding event (RR 0.92; 95% CI [0.77–1.09]; p = 0.32; I2 = 0%) for prasugrel compared with ticagrelor. Conclusion: There are no significant difference of MACE, all-cause mortality, cardiovascular mortality, MI, stent thrombosis, and bleeding between prasugrel and ticagrelor when added to aspirin among patients with ACS undergoing PCI.
KW - Clinical trial
KW - Complete
KW - Culprit
KW - Infarct related artery
KW - Revascularization
KW - STEMI
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U2 - 10.1016/j.carrev.2020.05.038
DO - 10.1016/j.carrev.2020.05.038
M3 - Review article
C2 - 32513604
AN - SCOPUS:85085950921
SN - 1553-8389
VL - 21
SP - 1613
EP - 1618
JO - Cardiovascular Revascularization Medicine
JF - Cardiovascular Revascularization Medicine
IS - 12
ER -