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Early outcome of early-goal directed therapy for patients with sepsis or septic shock: a systematic review and meta-analysis of randomized controlled trials

机译:败血症或败血性休克患者的早期目标指导治疗的早期结果:随机对照试验的系统评价和荟萃分析

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摘要

Various trials and meta-analyses have reported conflicting results concerning the application of early goal-directed therapy (EGDT) for sepsis and septic shock. The aim of this study was to update the evidence by performing a systematic review and meta-analysis. Multiple databases were searched from initial through August, 2016 for randomized controlled trials (RCTs) which investigated the associations between the use of EGDT and mortality in patients with sepsis or septic shock. Meta-analysis was performed using random-effects model and heterogeneity was examined through subgroup analyses. The primary outcome of interest was patient all-cause mortality including hospital or ICU mortality. Seventeen RCTs including 6207 participants with 3234 in the EGDT group and 2973 in the control group were eligible for this study. Meta-analysis showed that EGDT did not significantly reduce hospital or intensive care unit (ICU) mortality (relative risk [RR] 0.89, 95% CI 0.78 to 1.02) compared with control group for patients with sepsis or septic shock. The findings of subgroup analyses stratified by study region, number of research center, year of enrollment, clinical setting, sample size, timing of EGDT almost remained constant with that of the primary analysis. Our findings provide evidence that EGDT offers neutral survival effects for patients with sepsis or septic shock. Further meta-analyses based on larger well-designed RCTs or individual patient data meta-analysis are required to explore the survival benefits of EDGT in patients with sepsis or septic shock.
机译:各种试验和荟萃分析报告了有关脓毒症和败血性休克的早期目标导向疗法(EGDT)应用的矛盾结果。这项研究的目的是通过进行系统的审查和荟萃分析来更新证据。从最初到2016年8月,针对多个随机对照试验(RCT)搜索了多个数据库,这些试验研究了EGDT的使用与败血症或败血性休克患者的死亡率之间的关系。使用随机效应模型进行荟萃分析,并通过亚组分析检查异质性。感兴趣的主要结果是患者全因死亡率,包括医院或ICU死亡率。共有17项RCT(包括6207名参与者,其中EGDT组为3234名,对照组为2973名)符合这项研究的条件。荟萃分析显示,败血症或败血性休克患者与对照组相比,EGDT并未显着降低医院或重症监护病房(ICU)的死亡率(相对危险度[RR] 0.89,95%CI 0.78至1.02)。按研究区域,研究中心数量,入组年份,临床背景,样本量,EGDT时机分层的亚组分析结果与初次分析几乎保持不变。我们的发现提供了证据,证明EGDT对败血症或败血性休克患者具有中性生存作用。为了探索败血症或败血性休克患者EDGT的生存益处,需要基于较大的设计良好的RCT进行进一步的荟萃分析或对患者进行个体数据荟萃分析。

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