Meta-Analysis of Randomized Controlled Trials Comparing Risk of Major Adverse Cardiac Events and Bleeding in Patients With Prasugrel Versus Clopidogrel

The use of prasugrel in patients with coronary artery disease (CAD) has been associated with decreased major adverse cardiac events (MACEs) compared with clopidogrel but with an increased risk of bleeding. However, it remains unclear if the risks of bleeding outweigh those of MACEs in patients on pr...

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Veröffentlicht in:The American journal of cardiology 2015-08, Vol.116 (3), p.384-392
Hauptverfasser: Chen, Hai-Bin, MD, Zhang, Xin-Lu, MD, Liang, Hong-Bin, MD, Liu, Xue-Wei, MD, Zhang, Xin-Yu, MD, Huang, Bao-Yi, MD, Xiu, Jiancheng, MD, PhD
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container_title The American journal of cardiology
container_volume 116
creator Chen, Hai-Bin, MD
Zhang, Xin-Lu, MD
Liang, Hong-Bin, MD
Liu, Xue-Wei, MD
Zhang, Xin-Yu, MD
Huang, Bao-Yi, MD
Xiu, Jiancheng, MD, PhD
description The use of prasugrel in patients with coronary artery disease (CAD) has been associated with decreased major adverse cardiac events (MACEs) compared with clopidogrel but with an increased risk of bleeding. However, it remains unclear if the risks of bleeding outweigh those of MACEs in patients on prasugrel treatment. We systematically reviewed randomized controlled trials comparing prasugrel with clopidogrel in patients with CAD. We performed a literature search of PubMed, EMBASE, and Cochrane Central Register of Controlled Trial databases from inception to November 25, 2014, and reviewed the reference lists of retrieved articles. A comparative estimate was made for the combined rates of MACEs and bleeding from the same trials in the framework of this meta-analysis and expressed as odds ratios (ORs) and 95% confidence intervals (CIs) in both random- and fixed-effects models. Nine studies involving 25,214 patients were included in our meta-analysis. In both the random- and fixed-effects models, the risks of MACEs outweighed those of major bleeding (OR 7.48, 95% CI 3.75 to 14.94, p 
doi_str_mv 10.1016/j.amjcard.2015.04.054
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However, it remains unclear if the risks of bleeding outweigh those of MACEs in patients on prasugrel treatment. We systematically reviewed randomized controlled trials comparing prasugrel with clopidogrel in patients with CAD. We performed a literature search of PubMed, EMBASE, and Cochrane Central Register of Controlled Trial databases from inception to November 25, 2014, and reviewed the reference lists of retrieved articles. A comparative estimate was made for the combined rates of MACEs and bleeding from the same trials in the framework of this meta-analysis and expressed as odds ratios (ORs) and 95% confidence intervals (CIs) in both random- and fixed-effects models. Nine studies involving 25,214 patients were included in our meta-analysis. In both the random- and fixed-effects models, the risks of MACEs outweighed those of major bleeding (OR 7.48, 95% CI 3.75 to 14.94, p &lt;0.0001, random effects) and of minor bleeding (OR 3.77, 95% CI 1.73 to 8.22, p = 0.009, random effects). Results were corroborated in a standard-dose clopidogrel subgroup analysis (OR 7.46, 95% CI 3.54 to 15.68, p &lt;0.0001, and OR 6.44, 95% CI 2.80 to 14.80, p &lt;0.0001, random effects, respectively). In conclusion, despite the increased risk of bleeding associated with prasugrel treatment compared with clopidogrel, the risk of MACEs far outweighed the risk of bleeding.</description><identifier>ISSN: 0002-9149</identifier><identifier>EISSN: 1879-1913</identifier><identifier>DOI: 10.1016/j.amjcard.2015.04.054</identifier><identifier>PMID: 26051379</identifier><identifier>CODEN: AJCDAG</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Bias ; Cardiology ; Cardiovascular ; Clinical trials ; Collaboration ; Confidence intervals ; Coronary Artery Disease - drug therapy ; Global Health ; Heart attacks ; Hemorrhage - chemically induced ; Hemorrhage - epidemiology ; Humans ; Incidence ; Piperazines - adverse effects ; Piperazines - therapeutic use ; Platelet Aggregation Inhibitors - adverse effects ; Platelet Aggregation Inhibitors - therapeutic use ; Prasugrel Hydrochloride ; Purinergic P2Y Receptor Antagonists - adverse effects ; Purinergic P2Y Receptor Antagonists - therapeutic use ; Randomized Controlled Trials as Topic ; Regression analysis ; Risk Factors ; Studies ; Thiophenes - adverse effects ; Thiophenes - therapeutic use ; Ticlopidine - adverse effects ; Ticlopidine - analogs &amp; derivatives ; Ticlopidine - therapeutic use</subject><ispartof>The American journal of cardiology, 2015-08, Vol.116 (3), p.384-392</ispartof><rights>Elsevier Inc.</rights><rights>2015 Elsevier Inc.</rights><rights>Copyright © 2015 Elsevier Inc. All rights reserved.</rights><rights>Copyright Elsevier Limited Aug 1, 2015</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c518t-fe5b04355fcfa0655f8043d57dd3e1e08ea79c869e5826427c283ae1b9466b413</citedby><cites>FETCH-LOGICAL-c518t-fe5b04355fcfa0655f8043d57dd3e1e08ea79c869e5826427c283ae1b9466b413</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0002914915012527$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27903,27904,65309</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26051379$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Chen, Hai-Bin, MD</creatorcontrib><creatorcontrib>Zhang, Xin-Lu, MD</creatorcontrib><creatorcontrib>Liang, Hong-Bin, MD</creatorcontrib><creatorcontrib>Liu, Xue-Wei, MD</creatorcontrib><creatorcontrib>Zhang, Xin-Yu, MD</creatorcontrib><creatorcontrib>Huang, Bao-Yi, MD</creatorcontrib><creatorcontrib>Xiu, Jiancheng, MD, PhD</creatorcontrib><title>Meta-Analysis of Randomized Controlled Trials Comparing Risk of Major Adverse Cardiac Events and Bleeding in Patients With Prasugrel Versus Clopidogrel</title><title>The American journal of cardiology</title><addtitle>Am J Cardiol</addtitle><description>The use of prasugrel in patients with coronary artery disease (CAD) has been associated with decreased major adverse cardiac events (MACEs) compared with clopidogrel but with an increased risk of bleeding. However, it remains unclear if the risks of bleeding outweigh those of MACEs in patients on prasugrel treatment. We systematically reviewed randomized controlled trials comparing prasugrel with clopidogrel in patients with CAD. We performed a literature search of PubMed, EMBASE, and Cochrane Central Register of Controlled Trial databases from inception to November 25, 2014, and reviewed the reference lists of retrieved articles. A comparative estimate was made for the combined rates of MACEs and bleeding from the same trials in the framework of this meta-analysis and expressed as odds ratios (ORs) and 95% confidence intervals (CIs) in both random- and fixed-effects models. Nine studies involving 25,214 patients were included in our meta-analysis. In both the random- and fixed-effects models, the risks of MACEs outweighed those of major bleeding (OR 7.48, 95% CI 3.75 to 14.94, p &lt;0.0001, random effects) and of minor bleeding (OR 3.77, 95% CI 1.73 to 8.22, p = 0.009, random effects). Results were corroborated in a standard-dose clopidogrel subgroup analysis (OR 7.46, 95% CI 3.54 to 15.68, p &lt;0.0001, and OR 6.44, 95% CI 2.80 to 14.80, p &lt;0.0001, random effects, respectively). In conclusion, despite the increased risk of bleeding associated with prasugrel treatment compared with clopidogrel, the risk of MACEs far outweighed the risk of bleeding.</description><subject>Bias</subject><subject>Cardiology</subject><subject>Cardiovascular</subject><subject>Clinical trials</subject><subject>Collaboration</subject><subject>Confidence intervals</subject><subject>Coronary Artery Disease - drug therapy</subject><subject>Global Health</subject><subject>Heart attacks</subject><subject>Hemorrhage - chemically induced</subject><subject>Hemorrhage - epidemiology</subject><subject>Humans</subject><subject>Incidence</subject><subject>Piperazines - adverse effects</subject><subject>Piperazines - therapeutic use</subject><subject>Platelet Aggregation Inhibitors - adverse effects</subject><subject>Platelet Aggregation Inhibitors - therapeutic use</subject><subject>Prasugrel Hydrochloride</subject><subject>Purinergic P2Y Receptor Antagonists - adverse effects</subject><subject>Purinergic P2Y Receptor Antagonists - therapeutic use</subject><subject>Randomized Controlled Trials as Topic</subject><subject>Regression analysis</subject><subject>Risk Factors</subject><subject>Studies</subject><subject>Thiophenes - adverse effects</subject><subject>Thiophenes - therapeutic use</subject><subject>Ticlopidine - adverse effects</subject><subject>Ticlopidine - analogs &amp; 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However, it remains unclear if the risks of bleeding outweigh those of MACEs in patients on prasugrel treatment. We systematically reviewed randomized controlled trials comparing prasugrel with clopidogrel in patients with CAD. We performed a literature search of PubMed, EMBASE, and Cochrane Central Register of Controlled Trial databases from inception to November 25, 2014, and reviewed the reference lists of retrieved articles. A comparative estimate was made for the combined rates of MACEs and bleeding from the same trials in the framework of this meta-analysis and expressed as odds ratios (ORs) and 95% confidence intervals (CIs) in both random- and fixed-effects models. Nine studies involving 25,214 patients were included in our meta-analysis. In both the random- and fixed-effects models, the risks of MACEs outweighed those of major bleeding (OR 7.48, 95% CI 3.75 to 14.94, p &lt;0.0001, random effects) and of minor bleeding (OR 3.77, 95% CI 1.73 to 8.22, p = 0.009, random effects). Results were corroborated in a standard-dose clopidogrel subgroup analysis (OR 7.46, 95% CI 3.54 to 15.68, p &lt;0.0001, and OR 6.44, 95% CI 2.80 to 14.80, p &lt;0.0001, random effects, respectively). In conclusion, despite the increased risk of bleeding associated with prasugrel treatment compared with clopidogrel, the risk of MACEs far outweighed the risk of bleeding.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>26051379</pmid><doi>10.1016/j.amjcard.2015.04.054</doi><tpages>9</tpages></addata></record>
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subjects Bias
Cardiology
Cardiovascular
Clinical trials
Collaboration
Confidence intervals
Coronary Artery Disease - drug therapy
Global Health
Heart attacks
Hemorrhage - chemically induced
Hemorrhage - epidemiology
Humans
Incidence
Piperazines - adverse effects
Piperazines - therapeutic use
Platelet Aggregation Inhibitors - adverse effects
Platelet Aggregation Inhibitors - therapeutic use
Prasugrel Hydrochloride
Purinergic P2Y Receptor Antagonists - adverse effects
Purinergic P2Y Receptor Antagonists - therapeutic use
Randomized Controlled Trials as Topic
Regression analysis
Risk Factors
Studies
Thiophenes - adverse effects
Thiophenes - therapeutic use
Ticlopidine - adverse effects
Ticlopidine - analogs & derivatives
Ticlopidine - therapeutic use
title Meta-Analysis of Randomized Controlled Trials Comparing Risk of Major Adverse Cardiac Events and Bleeding in Patients With Prasugrel Versus Clopidogrel
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