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抗凝血酶III用于危重症患者:一项系统评价、荟萃分析及试验序贯分析

Antithrombin III for critically ill patients: a systematic review with meta-analysis and trial sequential analysis.

作者信息

Allingstrup Mikkel, Wetterslev Jørn, Ravn Frederikke B, Møller Ann Merete, Afshari Arash

机构信息

Department of Anaesthesia, Køge Sygehus, Copenhagen University Hospital, Copenhagen, Denmark.

Department of Paediatric and Obstetric Anaesthesia, Rigshospitalet, Copenhagen University Hospital, Copenhagen, Denmark.

出版信息

Intensive Care Med. 2016 Apr;42(4):505-520. doi: 10.1007/s00134-016-4225-7. Epub 2016 Feb 9.

Abstract

PURPOSE

Antithrombin III (AT III) is an anticoagulant with anti-inflammatory properties. We assessed the benefits and harms of AT III in critically ill patients.

METHODS

We searched from inception to 27 August 2015 in CENTRAL, MEDLINE, EMBASE, CAB, BIOSIS and CINAHL. We included randomized controlled trials (RCTs) irrespective of publication status, date of publication, blinding status, outcomes published or language.

RESULTS

We included 30 RCTs with a total of 3933 participants. The majority of included trials were at high risk of bias. Combining all trials, regardless of bias, showed no statistically significant effect of AT III on mortality (RR 0.95, 95% CI 0.88-1.03, I (2) = 0%, fixed-effect model, 29 trials, 3882 participants). Among those with severe sepsis and disseminated intravascular coagulation (DIC), AT III showed no impact on mortality (RR 0.95, 95% Cl 0.88-1.03, I (2) = 0%, fixed-effect model, 12 trials, 2858 participants). We carried out multiple subgroup and sensitivity analyses to assess the benefits and harms of AT III and to examine the impact of risk of bias. AT III significantly increased bleeding events (RR 1.58, 95% CI 1.35-1.84, I (2) = 0%, fixed-effect model, 11 trials, 3019 participants). However, for all other outcome measures and analyses, the results did not reach statistical significance.

CONCLUSIONS

There is insufficient evidence to support AT III substitution in any category of critically ill participants including those with sepsis and DIC. AT III did not show an impact on mortality, but increased the risk of bleeding.

摘要

目的

抗凝血酶III(AT III)是一种具有抗炎特性的抗凝剂。我们评估了AT III在重症重症危重症患者中的利弊。

方法

我们检索了从数据库建库至2015年8月27日的CENTRAL、MEDLINE、EMBASE、CAB、BIOSIS和CINAHL数据库。我们纳入了随机对照试验(RCT),无论其发表状态、发表日期、盲法状态、已发表的结局或语言如何。

结果

我们纳入了30项RCT,共3933名参与者。纳入的试验大多存在高偏倚风险。合并所有试验,无论有无偏倚,结果显示AT III对死亡率无统计学显著影响(风险比[RR]0.95,95%置信区间[CI]0.88 - 1.03,I² = 0%,固定效应模型,29项试验,3882名参与者)。在患有严重脓毒症和弥散性血管内凝血(DIC)的患者中,AT III对死亡率无影响(RR 0.95,95% CI 0.88 - 1.03,I² = 0%,固定效应模型,12项试验,2858名参与者)。我们进行了多项亚组分析和敏感性分析,以评估AT III的利弊,并检验偏倚风险的影响。AT III显著增加出血事件(RR 1.58,95% CI 1.35 - 1.84,I² = 0%,固定效应模型,11项试验,3019名参与者)。然而,对于所有其他结局指标和分析,结果均未达到统计学显著性。

结论

没有足够的证据支持在任何类型的危重症参与者(包括脓毒症和DIC患者)中使用AT III替代治疗。AT III对死亡率无影响,但增加了出血风险。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c220/7095103/dc34910b5474/134_2016_4225_Fig1_HTML.jpg

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