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用于登革热感染的皮质类固醇。

Corticosteroids for dengue infection.

作者信息

Zhang Fan, Kramer Christine V

机构信息

School of Public Health and Management, Chongqing Medical University, No. 1, Yi Xue Yuan Road, Chongqing, China, 400016.

出版信息

Cochrane Database Syst Rev. 2014 Jul 1;2014(7):CD003488. doi: 10.1002/14651858.CD003488.pub3.

DOI:10.1002/14651858.CD003488.pub3
PMID:24984082
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6555473/
Abstract

BACKGROUND

Dengue is a common and important mosquito-borne viral infection. In many low- and middle-income countries it is endemic and is an important public health problem. Severe dengue is an important cause of death in children. There is no specific treatment for dengue, but observational studies suggest corticosteroids may have a benefit in dengue-related shock, and some people believe corticosteroids may prevent the progression to severe illness if given early in the course of the illness.

OBJECTIVES

To compare treatment of dengue with and without use of corticosteroids or placebo in relation to preventing shock-related death and disease progression in children and adults.

SEARCH METHODS

We searched the Cochrane Infectious Disease Group Centralized Register; CENTRAL; MEDLINE; EMBASE; and LILACS, up to 6 January 2014. We screened reference lists and contacted the relevant study authors for additional information where required.

SELECTION CRITERIA

Randomized controlled trials or quasi-randomized controlled trials comparing corticosteroids with placebo or no corticosteroids in patients diagnosed with dengue-related shock, or patients in an early symptomatic state of dengue with positive serology.

DATA COLLECTION AND ANALYSIS

Two researchers independently screened eligibility of records, extracted data and assessed quality of the studies. We presented findings in meta-analysis and summary of findings tables and evaluated the quality of evidence using GRADE.

MAIN RESULTS

We included eight studies enrolling 948 participants in this review. Paitents with dengue-related shock Four studies enrolled children younger than 15 years with dengue-related shock at hospitals in Southeast Asia and evaluated intravenous corticosteroids. The trials did not detect an effect on death (four trials, 284 participants, very low quality evidence), the need for blood transfusion (two trials, 89 participants, very low quality evidence), pulmonary haemorrhage (one trial, 63 participants, very low quality evidence), convulsions (one trial, 63 participants, very low quality evidence), or duration of hospitalization (one trial, 63 participants, very low quality evidence). The body of evidence is too small to confidently prove or exclude clinically important effects. Furthermore, the trials are more than 20 years old with several methodological limitations. Patients with dengue at an early stage Four studies enrolled 664 children and adults with dengue at an early stage of infection (without shock) in Columbia, India, Sri Lanka and Vietnam. In these participants there were no evidence of effects of oral or intravenous corticosteroids on mortality (four trials, 664 participants, low quality evidence), or on the development of complications of severe dengue such as shock (two trials, 286 participants, very low quality evidence), severe bleeding (two trials, 425 participants, very low quality evidence), severe thrombocytopaenia (one trial, 225 participants, very low quality evidence), ascites (one trial, 178 participants, very low quality evidence) and intensive care unit (ICU) admissions (two trials, 286 participants, very low quality evidence).

AUTHORS' CONCLUSIONS: The evidence from trials using corticosteroids in dengue is inconclusive and the quality of evidence is low to very low. This applies to both the use of corticosteroids in dengue-related shock and for dengue at an early stage. There is insufficient evidence to evaluate the effects of corticosteroids in the treatment of early stage dengue fever and dengue-related shock outside of the context of a randomized controlled trial.

摘要

背景

登革热是一种常见且重要的蚊媒病毒感染。在许多低收入和中等收入国家,它呈地方性流行,是一个重要的公共卫生问题。重症登革热是儿童死亡的重要原因。登革热没有特效治疗方法,但观察性研究表明,皮质类固醇可能对登革热相关休克有益,一些人认为如果在病程早期给予皮质类固醇,可能会预防病情发展为重症。

目的

比较在儿童和成人中使用与不使用皮质类固醇或安慰剂治疗登革热在预防休克相关死亡和疾病进展方面的效果。

检索方法

我们检索了Cochrane传染病组中央注册库、CENTRAL、MEDLINE、EMBASE和LILACS,检索截止至2014年1月6日。我们筛选了参考文献列表,并在需要时联系相关研究的作者以获取更多信息。

选择标准

随机对照试验或半随机对照试验,比较皮质类固醇与安慰剂或不使用皮质类固醇在诊断为登革热相关休克的患者,或血清学阳性的登革热早期症状患者中的疗效。

数据收集与分析

两名研究人员独立筛选记录的合格性、提取数据并评估研究质量。我们在Meta分析和结果总结表中呈现研究结果,并使用GRADE评估证据质量。

主要结果

本综述纳入了8项研究,共948名参与者。登革热相关休克患者:4项研究纳入了东南亚医院中15岁以下患有登革热相关休克的儿童,并评估了静脉注射皮质类固醇的效果。这些试验未发现对死亡(4项试验,284名参与者,极低质量证据)、输血需求(2项试验,89名参与者,极低质量证据)、肺出血(1项试验,63名参与者,极低质量证据)、惊厥(1项试验,63名参与者,极低质量证据)或住院时间(1项试验,63名参与者,极低质量证据)有影响。证据体量过小,无法确定地证明或排除临床重要影响。此外,这些试验已有20多年历史,存在若干方法学局限性。登革热早期患者:4项研究纳入了哥伦比亚、印度、斯里兰卡和越南664名处于感染早期(无休克)的登革热儿童和成人。在这些参与者中,没有证据表明口服或静脉注射皮质类固醇对死亡率(4项试验,664名参与者,低质量证据),或对重症登革热并发症的发生,如休克(2项试验,286名参与者,极低质量证据)、严重出血(2项试验,425名参与者,极低质量证据)、严重血小板减少症(1项试验,225名参与者,极低质量证据)、腹水(1项试验,178名参与者,极低质量证据)和重症监护病房(ICU)收治(2项试验,286名参与者,极低质量证据)有影响。

作者结论

使用皮质类固醇治疗登革热的试验证据尚无定论,证据质量低至极低。这适用于皮质类固醇在登革热相关休克和登革热早期的使用。在随机对照试验背景之外,没有足够的证据来评估皮质类固醇在治疗早期登革热发热和登革热相关休克中的效果。

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