A comparison of cangrelor, prasugrel, ticagrelor, and clopidogrel in patients undergoing percutaneous coronary intervention: A network meta-analysis. - 2016

Available in print through MWHC library: 2002 - present

BACKGROUND: Newer P2Y12 inhibitors have more rapid onset of platelet inhibition compared with clopidogrel, especially the intravenous P2Y12 inhibitor cangrelor. Direct comparisons between cangrelor and oral P2Y12 inhibitors ticagrelor and prasugrel do not exist. Thus, we performed a network meta-analysis to directly and indirectly compare different P2Y12 inhibitors in patients undergoing percutaneous coronary intervention (PCI). CONCLUSION: Despite rapid platelet inhibition provided by cangrelor, newer oral P2Y12 inhibitors such as ticagrelor and prasugrel have comparable clinical outcomes. Copyright (c) 2016 Elsevier Inc. All rights reserved. METHODS: MEDLINE/PubMed and ClinicalTrials.gov were searched for randomized controlled trials (RCTs) that compared at least two P2Y12 inhibitors including cangrelor, clopidogrel, prasugrel, and ticagrelor. Network meta-analysis with a Bayesian approach was performed to directly and indirectly compare the effects of the aforementioned P2Y12 inhibitors on clinical outcomes. Odds ratios with credible intervals (OR [CrIs]) were generated with random-effects models to compare outcomes. RESULTS: This analysis included 15 RCTs with 54,025 patients randomized to cangrelor (n=12,475), clopidogrel (n=26,903), prasugrel (n=7455), or ticagrelor (n=7192) at time of PCI. Patients had a mean age of 63+/-10, 74% were male, and 82% underwent PCI for acute coronary syndrome. No significant differences between cangrelor and clopidogrel were found with respect to cardiovascular death (OR 1.01 [CrI 0.23-4.39]), myocardial infarction (OR 0.94 [CrI 0.69-1.25]), major adverse cardiac events (OR 0.91 [CrI 0.69-1.18]), stent thrombosis (OR 0.66 [CrI 0.37-1.19]), or major bleeding (OR 1.52 [CrI 0.79-2.98]). Rank probability data suggested that ticagrelor and prasugrel were better than cangrelor for reducing ischemic events, though these differences were not significant.


English

1878-0938


*Adenosine Monophosphate/aa [Analogs & Derivatives]
*Adenosine/aa [Analogs & Derivatives]
*Percutaneous Coronary Intervention
*Platelet Aggregation Inhibitors/tu [Therapeutic Use]
*Prasugrel Hydrochloride/tu [Therapeutic Use]
*Purinergic P2Y Receptor Antagonists/tu [Therapeutic Use]
*Ticlopidine/aa [Analogs & Derivatives]
Adenosine Monophosphate/ae [Adverse Effects]
Adenosine Monophosphate/tu [Therapeutic Use]
Adenosine/ae [Adverse Effects]
Adenosine/tu [Therapeutic Use]
Humans
Myocardial Infarction/dt [Drug Therapy]
Network Meta-Analysis
Percutaneous Coronary Intervention/mt [Methods]
Platelet Aggregation Inhibitors/ad [Administration & Dosage]
Prasugrel Hydrochloride/ae [Adverse Effects]
Purinergic P2Y Receptor Antagonists/ae [Adverse Effects]
Ticlopidine/ae [Adverse Effects]
Ticlopidine/tu [Therapeutic Use]
Treatment Outcome


MedStar Heart & Vascular Institute


Journal Article