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儿童短期口服皮质类固醇毒性的系统评价

Systematic review of the toxicity of short-course oral corticosteroids in children.

作者信息

Aljebab Fahad, Choonara Imti, Conroy Sharon

机构信息

Division of Medical Sciences & Graduate Entry Medicine, School of Medicine, University of Nottingham, Royal Derby Hospital Centre, Derby, UK.

出版信息

Arch Dis Child. 2016 Apr;101(4):365-70. doi: 10.1136/archdischild-2015-309522. Epub 2016 Jan 14.

Abstract

BACKGROUND

Short-course oral corticosteroids are commonly used in children but are known to be associated with adverse drug reactions (ADRs). This review aimed to identify the most common and serious ADRs and to determine their relative risk levels.

METHODS

A literature search of EMBASE, MEDLINE, International Pharmaceutical Abstracts, CINAHL, Cochrane Library and PubMed was performed with no language restrictions to identify studies in which oral corticosteroids were administered to patients aged 28 days to 18 years of age for up to and including 14 days of treatment. Each database was searched from their earliest dates to December 2013. All studies providing clear information on ADRs were included.

RESULTS

Thirty-eight studies including 22 randomised controlled trials (RCTs) met the inclusion criteria. The studies involved a total of 3200 children in whom 850 ADRs were reported. The three most frequent ADRs were vomiting, behavioural changes and sleep disturbance, with respective incidence rates of 5.4%, 4.7% and 4.3% of patients assessed for these ADRs. Infection was one of the most serious ADRs; one child died after contracting varicella zoster. When measured, 144 of 369 patients showed increased blood pressure; 21 of 75 patients showed weight gain; and biochemical hypothalamic-pituitary-adrenal axis suppression was detected in 43 of 53 patients.

CONCLUSIONS

Vomiting, behavioural changes and sleep disturbance were the most frequent ADRs seen when short-course oral corticosteroids were given to children. Increased susceptibility to infection was the most serious ADR.

TRIAL REGISTRATION NUMBER

CRD42014008774. By PROSPERO International prospective register of systematic reviews.

摘要

背景

短疗程口服糖皮质激素常用于儿童,但已知会引发药物不良反应(ADR)。本综述旨在确定最常见和最严重的ADR,并确定其相对风险水平。

方法

对EMBASE、MEDLINE、国际药学文摘、护理学与健康领域数据库(CINAHL)、Cochrane图书馆和PubMed进行文献检索,无语言限制,以确定对年龄在28天至18岁的患者给予口服糖皮质激素治疗长达14天(包括14天)的研究。每个数据库从最早日期检索至2013年12月。纳入所有提供ADR明确信息的研究。

结果

38项研究(包括22项随机对照试验)符合纳入标准。这些研究共涉及3200名儿童,报告了850例ADR。三种最常见的ADR是呕吐、行为改变和睡眠障碍,接受这些ADR评估的患者发生率分别为5.4%、4.7%和4.3%。感染是最严重的ADR之一;1名儿童感染水痘带状疱疹后死亡。在接受测量的患者中,369例中有144例血压升高;75例中有21例体重增加;53例中有43例检测到生化下丘脑-垂体-肾上腺轴抑制。

结论

对儿童给予短疗程口服糖皮质激素时,呕吐、行为改变和睡眠障碍是最常见的ADR。感染易感性增加是最严重的ADR。

试验注册号

CRD42014008774。由PROSPERO国际系统评价前瞻性注册库提供。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8f57/4819633/bf7e358d3ca6/archdischild-2015-309522f01.jpg

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