Williams Phoebe C M, Berkley James A
a Nuffield Department of Clinical Medicine , The University of Oxford , Oxford , UK.
b Kenya Medical Research Institute (KEMRI)/Wellcome Trust Research Programme , Kilifi , Kenya.
Paediatr Int Child Health. 2018 Nov;38(sup1):S16-S31. doi: 10.1080/20469047.2017.1409452.
Background Vibrio cholerae is a highly motile Gram-negative bacterium which is responsible for 3 million cases of diarrhoeal illness and up to 100,000 deaths per year, with an increasing burden documented over the past decade. Current WHO guidelines for the treatment of paediatric cholera infection (tetracycline 12.5 mg/kg four times daily for 3 days) are based on data which are over a decade old. In an era of increasing antimicrobial resistance, updated review of the appropriate empirical therapy for cholera infection in children (taking account of susceptibility patterns, cost and the risk of adverse events) is necessary. Methods A systematic review of the current published literature on the treatment of cholera infection in accordance with the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) was undertaken. International clinical guidelines and studies pertaining to adverse effects associated with treatments available for cholera infection were also reviewed. Results The initial search produced 256 results, of which eight studies met the inclusion criteria. Quality assessment of the studies was performed as per the Grading of Recommendations Assessment, Development and Evaluation guidelines. Conclusions In view of the changing non-susceptibility rates worldwide, empirical therapy for cholera infection in paediatric patients should be changed to single-dose azithromycin (20 mg/kg), a safe and effective medication with ease of administration. Erythromycin (12.5 mg/kg four times daily for 3 days) exhibits similar bacteriological and clinical success and should be listed as a second-line therapy. Fluid resuscitation remains the cornerstone of management of paediatric cholera infection, and prevention of infection by promoting access to clean water and sanitation is paramount.
霍乱弧菌是一种高度运动性的革兰氏阴性菌,每年导致300万例腹泻病,多达10万人死亡,且在过去十年中记录的负担不断增加。世界卫生组织目前关于儿童霍乱感染治疗的指南(四环素12.5毫克/千克,每日4次,共3天)是基于十多年前的数据。在抗菌药物耐药性不断增加的时代,有必要对儿童霍乱感染的适当经验性治疗进行更新审查(考虑到药敏模式、成本和不良事件风险)。方法:根据系统评价和Meta分析的首选报告项目(PRISMA)对目前已发表的关于霍乱感染治疗的文献进行系统评价。还审查了与霍乱感染可用治疗相关的国际临床指南和不良反应研究。结果:初步检索产生256条结果,其中八项研究符合纳入标准。根据推荐分级评估、制定和评价指南对研究进行质量评估。结论:鉴于全球范围内不断变化的非敏感性率,儿童霍乱感染的经验性治疗应改为单剂量阿奇霉素(20毫克/千克),这是一种安全有效的药物,易于给药。红霉素(12.5毫克/千克,每日4次,共3天)显示出相似的细菌学和临床疗效,应列为二线治疗。液体复苏仍然是儿童霍乱感染管理的基石,通过促进获得清洁水和卫生设施来预防感染至关重要。