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Comparison of heparin, bivalirudin, and different glycoprotein IIb/IIIa inhibitor regimens for anticoagulation during percutaneous coronary intervention: A network meta-analysis.
- Source :
-
Cardiovascular revascularization medicine : including molecular interventions [Cardiovasc Revasc Med] 2016 Dec; Vol. 17 (8), pp. 535-545. Date of Electronic Publication: 2016 Sep 30. - Publication Year :
- 2016
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Abstract
- Background/purpose: Numerous GPIs are available for PCI. Although they were tested in randomized controlled trials, a comparison between the different GPI strategies is lacking. Thus, we performed a Bayesian network meta-analysis to compare different glycoprotein IIb/IIIa inhibitor (GPI) strategies with heparin and bivalirudin for percutaneous coronary intervention (PCI).<br />Methods: MEDLINE, Cochrane CENTRAL, and ClinicalTrials.gov were searched by two independent reviewers for randomized controlled trials comparing high-dose bolus tirofiban, abciximab, eptifibatide, heparin with provisional glycoprotein IIb/IIIa inhibitors, and bivalirudin with provisional GPI that reported clinical outcomes. Mixed treatment comparison model generation was performed to directly and indirectly compare between different anticoagulation strategies for all-cause mortality, myocardial infarction, major adverse cardiovascular events, major bleeding, minor bleeding, need for transfusion, and thrombocytopenia.<br />Results: A total of 41 randomized controlled trials with 38,645 patients were included in the analysis, among which 2654 were randomized to high-dose bolus tirofiban, 6752 to abciximab, 1669 to eptifibatide, 16,500 to heparin, and 11,070 to bivalirudin. Mean age was 64±11years, 75% were male, 91% were treated with stenting, 71% with clopidogrel, and 74% for acute coronary syndrome. High-dose bolus tirofiban was associated with a significant reduction in all-cause mortality compared with heparin (OR 0.57 [credible intervals 0.37, 0.9]) and eptifibatide (OR 0.44 [credible intervals 0.19, 1.0]). GPI regimens had less myocardial infarction and major adverse cardiovascular events but greater bleeding compared with heparin and bivalirudin. There was no difference among the GPI therapies for other outcomes, including myocardial infarction, major adverse cardiovascular events, and major bleeding.<br />Conclusions: Our network meta-analysis of 38,645 patients demonstrated that GPI regimens were associated with a reduction in recurrent myocardial infarction or major adverse cardiovascular events for PCI, while bivalirudin was associated with the lowest risk of bleeding.<br /> (Copyright © 2016. Published by Elsevier Inc.)
- Subjects :
- Aged
Anticoagulants adverse effects
Bayes Theorem
Blood Transfusion
Coronary Thrombosis diagnosis
Coronary Thrombosis etiology
Coronary Thrombosis mortality
Drug Therapy, Combination
Female
Hemorrhage chemically induced
Hemorrhage therapy
Heparin adverse effects
Hirudins adverse effects
Humans
Male
Middle Aged
Myocardial Infarction diagnosis
Myocardial Infarction etiology
Myocardial Infarction mortality
Peptide Fragments adverse effects
Percutaneous Coronary Intervention adverse effects
Percutaneous Coronary Intervention mortality
Platelet Aggregation Inhibitors adverse effects
Recombinant Proteins administration & dosage
Recombinant Proteins adverse effects
Risk Assessment
Risk Factors
Thrombocytopenia chemically induced
Thrombocytopenia therapy
Time Factors
Treatment Outcome
Anticoagulants administration & dosage
Coronary Thrombosis prevention & control
Heparin administration & dosage
Hirudins administration & dosage
Myocardial Infarction prevention & control
Peptide Fragments administration & dosage
Platelet Aggregation Inhibitors administration & dosage
Platelet Glycoprotein GPIIb-IIIa Complex antagonists & inhibitors
Subjects
Details
- Language :
- English
- ISSN :
- 1878-0938
- Volume :
- 17
- Issue :
- 8
- Database :
- MEDLINE
- Journal :
- Cardiovascular revascularization medicine : including molecular interventions
- Publication Type :
- Academic Journal
- Accession number :
- 27842901
- Full Text :
- https://doi.org/10.1016/j.carrev.2016.09.011