Effect of post-primary percutaneous coronary intervention bivalirudin infusion on net adverse clinical events and mortality: A comprehensive pairwise and network meta-analysis of randomized controlled trials

被引:8
作者
Shah, Rahman [1 ,2 ]
Matin, Khalid [3 ]
Rogers, Kelly C. [4 ]
Rao, Sunil V. [5 ]
机构
[1] Univ Tennessee, Sect Cardiol, Sch Med, Memphis, TN USA
[2] Vet Affairs Med Ctr, Memphis, TN USA
[3] Virginia Commonwealth Univ, Sect Hematol, Richmond, VA USA
[4] Univ Tennessee, Coll Pharm, Memphis, TN USA
[5] Duke Clin Res Inst, Durham, NC USA
关键词
bivalirudin; primary percutaneous coronary intervention; mortality; ACUTE STENT THROMBOSIS; HEPARIN; CLOPIDOGREL; OUTCOMES; IMPACT; PLUS;
D O I
10.1002/ccd.26859
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
ObjectiveTo compare the efficacies of various post-percutaneous coronary intervenetion (PCI) bivalirudin doses on net adverse clinical events (NACEs) and mortality. BackgroundIn primary PCI, lower risk of bleeding with bivalirudin (vs. unfractionated heparin [UFH]) is counterbalanced by an increased risk of acute stent thrombosis (ST). Several randomized clinical trials (RCTs) and a recent meta-analysis suggest that acute ST risk may be eliminated without compromising the bleeding benefit, but only if the full dose, not a low dose, of bivalirudin is continued post-PCI. However, it is not known whether this improved risk leads to lower rates of NACEs and mortality. MethodsScientific databases and Web sites were searched for RCTs. Trials were included if study patients were undergoing primary PCI for acute ST-segment elevation myocardial infarction and were randomly assigned to bivalirudin or UFH treatment. The bivalirudin arm was divided based on post-PCI bivalirudin dosage: The Biv-Full group received 1.75 mg/kg/h, the Biv-Low group, 0.25 mg/kg/h, and the Biv-No group, none. ResultsSix RCTs involving 16,842 patients were found. In pairwise meta-analysis, bivalirudin improved 30-day all-cause mortality by 35% and cardiac mortality by 32%, but did not yield a NACE rate better than that achieved with UFH. Subgroup analysis showed the Biv-Full group had a 46% lower NACE rate and 47% lower all-cause mortality than UFH. These effects were not seen in the other two groups. Network meta-analysis yielded similar results. At treatment ranking, the Biv-Full group yielded the best treatment efficacy. ConclusionsIn primary PCI, full-dose bivalirudin infusion for 3-4 hr after PCI appeared to improve NACE rates compared to UFH. It also seemed to be the most effective strategy for improving cardiac mortality and all-cause mortality. (c) 2016 Wiley Periodicals, Inc.
引用
收藏
页码:196 / 204
页数:9
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