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袢利尿剂用于伴有液体超负荷的成年重症监护患者:一项包含荟萃分析和试验序贯分析的随机临床试验系统评价

Loop diuretics in adult intensive care patients with fluid overload: a systematic review of randomised clinical trials with meta-analysis and trial sequential analysis.

作者信息

Wichmann Sine, Barbateskovic Marija, Liang Ning, Itenov Theis Skovsgaard, Berthelsen Rasmus Ehrenfried, Lindschou Jane, Perner Anders, Gluud Christian, Bestle Morten Heiberg

机构信息

Department of Anaesthesiology, Copenhagen University Hospital - North Zealand, Dyrehavevej 29, 3400, Hillerød, Denmark.

Copenhagen Trial Unit, Centre for Clinical Intervention Research, Copenhagen University Hospital-Rigshospitalet, Blegdamsvej 9, 2100, Copenhagen, Denmark.

出版信息

Ann Intensive Care. 2022 Jun 13;12(1):52. doi: 10.1186/s13613-022-01024-6.

DOI:10.1186/s13613-022-01024-6
PMID:35696008
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9192894/
Abstract

BACKGROUND

Fluid overload is a risk factor for organ dysfunction and death in intensive care unit (ICU) patients, but no guidelines exist for its management. We systematically reviewed benefits and harms of a single loop diuretic, the predominant treatment used for fluid overload in these patients.

METHODS

We conducted a systematic review with meta-analysis and Trial Sequential Analysis (TSA) of a single loop diuretic vs. other interventions reported in randomised clinical trials, adhering to our published protocol, the Cochrane Handbook, and PRISMA statement. We assessed the risks of bias with the ROB2-tool and certainty of evidence with GRADE. This study was registered in the International Prospective Register of Systematic Reviews (PROSPERO) (CRD42020184799).

RESULTS

We included 10 trials (804 participants), all at overall high risk of bias. For loop diuretics vs. placebo/no intervention, we found no difference in all-cause mortality (relative risk (RR) 0.72, 95% confidence interval (CI) 0.49-1.06; 4 trials; 359 participants; I = 0%; TSA-adjusted CI 0.15-3.48; very low certainty of evidence). Fewer serious adverse events were registered in the group treated with loop diuretics (RR 0.81, 95% CI 0.66-0.99; 6 trials; 476 participants; I = 0%; very low certainty of evidence), though contested by TSA (TSA-adjusted CI 0.55-1.20).

CONCLUSIONS

The evidence is very uncertain about the effect of loop diuretics on mortality and serious adverse events in adult ICU patients with fluid overload. Loop diuretics may reduce the occurrence of these outcomes, but large randomised placebo-controlled trials at low risk of bias are needed.

摘要

背景

液体超负荷是重症监护病房(ICU)患者发生器官功能障碍和死亡的一个危险因素,但目前尚无针对其管理的指南。我们系统回顾了单一袢利尿剂(这些患者中用于治疗液体超负荷的主要药物)的益处和危害。

方法

我们按照已发表的方案、Cochrane手册和PRISMA声明,对随机临床试验中报道的单一袢利尿剂与其他干预措施进行了系统回顾,并进行了荟萃分析和试验序贯分析(TSA)。我们使用ROB2工具评估偏倚风险,使用GRADE评估证据的确定性。本研究已在国际前瞻性系统评价注册库(PROSPERO)中注册(注册号:CRD42020184799)。

结果

我们纳入了10项试验(804名参与者),所有试验总体偏倚风险较高。对于袢利尿剂与安慰剂/无干预措施的比较,我们发现全因死亡率无差异(相对风险(RR)0.72,95%置信区间(CI)0.49 - 1.06;4项试验;359名参与者;I² = 0%;TSA调整后的CI 0.15 - 3.48;证据确定性极低)。接受袢利尿剂治疗的组中登记的严重不良事件较少(RR 0.81,95% CI 0.66 - 0.99;6项试验;476名参与者;I² = 0%;证据确定性极低),不过TSA对此提出了质疑(TSA调整后的CI 0.55 - 1.20)。

结论

关于袢利尿剂对成年液体超负荷ICU患者死亡率和严重不良事件的影响,证据非常不确定。袢利尿剂可能会降低这些结局的发生率,但需要开展大量偏倚风险低的随机安慰剂对照试验。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b41d/9192894/b98861651484/13613_2022_1024_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b41d/9192894/20d1358f28ee/13613_2022_1024_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b41d/9192894/c37d8dbc428b/13613_2022_1024_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b41d/9192894/b98861651484/13613_2022_1024_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b41d/9192894/20d1358f28ee/13613_2022_1024_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b41d/9192894/c37d8dbc428b/13613_2022_1024_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b41d/9192894/b98861651484/13613_2022_1024_Fig3_HTML.jpg

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