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Safety and efficacy of early administration of tirofiban in patients with acute ST-segment elevation myocardial infarction undergoing primary percutaneous coronary intervention: a meta-analysis / 中华医学杂志(英文版)
Chinese Medical Journal ; (24): 1126-1132, 2014.
Article in English | WPRIM (Western Pacific) | ID: wpr-253187
Responsible library: WPRO
ABSTRACT
<p><b>BACKGROUND</b>Tirofiban has been widely used as an adjunctive pharmacologic agent for revascularization in patients undergoing percutaneous coronary intervention, and the outcomes appear attractive. However, the potential benefits from early administration of tirofiban in patients with acute ST-segment elevation myocardial infarction (STEMI) undergoing primary percutaneous coronary intervention (PPCI) remain unclear.</p><p><b>METHODS</b>We conducted a search in MEDLINE, EMBASE, and the Cochrane Central Register of Controlled Trials up to September 2012 without language restriction. A total of eight randomized trials (n = 1 577 patients) comparing early (emergency department or ambulance) versus late (catheterization laboratory) administration of tirofiban in STEMI patients undergoing PPCI were included in this meta-analysis. Risk ratio (RR) was computed from individual studies and pooled with random- or fixed-effect models.</p><p><b>RESULTS</b>There were no differences in post-procedural Thrombolysis In Myocardial Infarction (TIMI) flow grade 3 and Corrected TIMI Frame Count (RR = 1.02, 95% confidence interval (CI) 0.99-1.05, P = 0.18; weighted mean difference (WMD) = -0.93, 95% CI -5.37-3.52, P = 0.68, respectively) between the two groups. Similarly, there were no significant differences in the incidence of 30-day mortality (RR = 1.69, 95% CI 0.69-4.13, P = 0.25) and re-myocardial infarction (RR = 0.71, 95% CI 0.21-2.35, P = 0.57) between early and late administration of tirofiban. As to the safety end points, no significant difference was observed in hospital minor bleeding (RR = 1.08, 95% CI 0.54-2.14, P = 0.83) and hospital and 30-day major bleeding between the two groups (RR = 0.98, 95% CI 0.46-2.10, P = 0.96; RR = 1.32, 95% CI 0.59-2.97, P = 0.49, respectively).</p><p><b>CONCLUSIONS</b>Early administration of tirofiban in patients undergoing PPCI for STEMI was safe, but no beneficial effects on post-procedural angiographic or clinical outcomes could be identified as compared with late administration. Besides the negative finding, more high-quality randomized clinical trials are still needed to explore the efficacy of adequate, earlier administration of tirofiban in patients undergoing PPCI.</p>
Subject(s)
Full text: Available Health context: SDG3 - Target 3.4 Reduce premature mortality due to noncommunicable diseases Health problem: Cardiovascular Disease / Ischemic Heart Disease Database: WPRIM (Western Pacific) Main subject: General Surgery / Tyrosine / Thrombolytic Therapy / Therapeutic Uses / Drug Therapy / Fibrinolytic Agents / Percutaneous Coronary Intervention / Methods / Myocardial Infarction Type of study: Controlled clinical trial / Prognostic study / Systematic review Limits: Humans Language: English Journal: Chinese Medical Journal Year: 2014 Document type: Article
Full text: Available Health context: SDG3 - Target 3.4 Reduce premature mortality due to noncommunicable diseases Health problem: Cardiovascular Disease / Ischemic Heart Disease Database: WPRIM (Western Pacific) Main subject: General Surgery / Tyrosine / Thrombolytic Therapy / Therapeutic Uses / Drug Therapy / Fibrinolytic Agents / Percutaneous Coronary Intervention / Methods / Myocardial Infarction Type of study: Controlled clinical trial / Prognostic study / Systematic review Limits: Humans Language: English Journal: Chinese Medical Journal Year: 2014 Document type: Article
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