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聚维酮碘-固定化血液灌流与脓毒症/感染性休克成年危重症患者死亡率:系统评价与荟萃分析及试验序贯分析。

Polymyxin B-immobilized hemoperfusion and mortality in critically ill adult patients with sepsis/septic shock: a systematic review with meta-analysis and trial sequential analysis.

机构信息

Department of Epidemiology and Preventive Medicine, Kyoto University Graduate School of Medicine, Yoshida Hon-machi, Sakyo-ku, Kyoto, Japan.

Japan Society for the Promotion of Science, 5-3-1 Kojimachi, Chiyoda-ku, Tokyo, Japan.

出版信息

Intensive Care Med. 2018 Feb;44(2):167-178. doi: 10.1007/s00134-017-5004-9. Epub 2017 Dec 4.

Abstract

PURPOSE

Polymyxin B-immobilized hemoperfusion (PMX-HP) is an adjuvant therapy for sepsis or septic shock that clears circulating endotoxin. Prior trials have shown that PMX-HP improves surrogate endpoints. We aimed to conduct an evidence synthesis to evaluate the efficacy and safety of PMX-HP in critically ill adult patients with sepsis or septic shock.

METHODS

We searched for randomized controlled trials (RCTs) in MEDLINE, EMBASE, the Cochrane Library, the Health Technology Assessment Database, CINAHL, "Igaku Chuo Zasshi", the National Institute of Health Clinical Trials Register, the World Health Organization International Clinical Trials Registry Platform, the University Hospital Medical Information Network Clinical Trials Registry, the reference lists of retrieved articles, and publications by manufacturers of PMX-HP. The primary outcomes were 28-day all-cause mortality, the number of patients with at least one serious adverse event, and organ dysfunction scores. The GRADE methodology for the certainty of evidence was used.

RESULTS

Six trials (857 participants; weighted mean age 62.5 years) proved eligible. Patient-oriented primary outcomes were assessed. The pooled risk ratio (RR) for 28-day mortality associated with PMX-HP was 1.03 [95% confidence interval (CI) 0.78-1.36; I  = 25%; n = 797]. The pooled RR for adverse events was 2.17 (95% CI 0.68-6.94; I  = 0%; n = 717). Organ dysfunction scores over 24-72 h after PMX-HP treatment did not change significantly (standardized mean difference - 0.26; 95% CI - 0.64 to 0.12; I  = 78%; n = 797). The certainty of the body of evidence was judged as low for both benefit and harm using the GRADE methodology.

CONCLUSIONS

There is currently insufficient evidence to support the routine use of PMX-HP to treat patients with sepsis or septic shock.

REGISTRATION

PROSPERO International Prospective Register of Systematic Reviews (CRD42016038356).

摘要

目的

多黏菌素 B 免疫吸附血液灌流(PMX-HP)是一种辅助治疗败血症或感染性休克的方法,可清除循环内毒素。先前的试验表明,PMX-HP 可改善替代终点。我们旨在进行一项证据综合评估,以评估 PMX-HP 对患有败血症或感染性休克的危重症成年患者的疗效和安全性。

方法

我们在 MEDLINE、EMBASE、Cochrane 图书馆、卫生技术评估数据库、CINAHL、“Igaku Chuo Zasshi”、美国国立卫生研究院临床试验注册处、世界卫生组织国际临床试验注册平台、大学医院医疗信息网络临床试验注册处、检索文章的参考文献列表以及 PMX-HP 制造商的出版物中搜索随机对照试验(RCT)。主要结局为 28 天全因死亡率、至少有一个严重不良事件的患者数量和器官功能障碍评分。使用 GRADE 方法评估证据的确定性。

结果

六项试验(857 名参与者;加权平均年龄 62.5 岁)被证明符合条件。评估了以患者为中心的主要结局。PMX-HP 相关 28 天死亡率的合并风险比(RR)为 1.03 [95%置信区间(CI)0.78-1.36;I²=25%;n=797]。不良事件的合并 RR 为 2.17(95%CI 0.68-6.94;I=0%;n=717)。PMX-HP 治疗后 24-72 小时器官功能障碍评分无明显变化(标准化均数差-0.26;95%CI-0.64 至 0.12;I²=78%;n=797)。使用 GRADE 方法,证据体的获益和危害确定性均被判定为低质量。

结论

目前尚无足够证据支持常规使用 PMX-HP 治疗败血症或感染性休克患者。

注册

PROSPERO 国际前瞻性系统评价注册库(CRD42016038356)。

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