Minaz Anmol, Alam Ridwa, Jiwani Uswa, Vadsaria Khadija, Khan Ahmad, Ishaq Aqsa, Sultan Samar, Mohsin Marium, Sharif Ashraf, Nisar Yasir Bin, Das Jai K, Soofi Sajid, Ariff Shabina
Centre of Excellence in Women and Child Health, Aga Khan University, Karachi, Pakistan.
University Library, Aga Khan University, Karachi, Pakistan.
J Glob Health. 2024 Dec 20;14:04236. doi: 10.7189/jogh.14.04236.
Numerous studies have investigated the efficacy of probiotics in treating acute and persistent diarrhoea. However, probiotics have not been established as a recommended management option for diarrhoeal illness by the World Health Organization (WHO). Therefore, we conducted a systematic review of randomised controlled trials to assess the efficacy of probiotics for the management of acute and persistent diarrhoea in children.
A systematic search on PubMed, CINAHL, Wiley Cochrane Library, Scopus, Clinicaltrials.gov, and WHO International Clinical Trials Registry Platform (ICTRP) was performed. All studies published in the year 2000 and onwards that assessed the use of probiotics in the management of acute and persistent diarrhoea in children aged 0-10 years were included. The risk of bias was assessed using the Cochrane Risk of Bias II (RoB-2) tool and the quality of evidence was assessed using the Grading of Recommendations, Assessment, Development, and Evaluations (GRADE) approach. This review was commissioned by WHO for revision of their guidelines for childhood diarrhoea management.
The review included 98 studies with a total of 17 236 participants. Studies were categorised based on the WHO definition of diarrhoea or author-specified definition. In studies considering the WHO definition of diarrhoea, the probiotics group was more likely to achieve clinical cure (risk ratio = 1.12 (95% confidence interval (CI) = 1.01, 1.24, studies = 14)) and reduce the duration of diarrhoea (mean difference = -13.27 hours (95% CI = -16.72, -9.83, studies = 33)) than the control group in children with acute diarrhoea. However, the effect size was small, and statistical heterogeneity was very high, leading to low certainty of evidence. In children with persistent diarrhoea, probiotics reduced the duration of diarrhoea by 95 hours (mean difference = -96.45 (95% CI = -110.53, -82.37, studies = 2)), but the certainty of the evidence was very low.
The results from this systematic review suggest low certainty of evidence for the effect of probiotics on clinical cure and duration of diarrhoea in children. There was significant diversity in the genus, species, dosages, and duration of treatment in the trial and administration. High levels of heterogeneity reduced the certainty of evidence. Large-scale randomised clinical trials are needed to evaluate specific probiotic strains and doses. In addition, cost-effective analysis studies are needed to be explored in future research.
The protocol for this review was registered with the International Prospective Register of Systematic Reviews (PROSPERO: CRD42023449200).
众多研究探讨了益生菌治疗急性和持续性腹泻的疗效。然而,世界卫生组织(WHO)尚未将益生菌确立为腹泻疾病的推荐管理选项。因此,我们进行了一项随机对照试验的系统评价,以评估益生菌治疗儿童急性和持续性腹泻的疗效。
在PubMed、CINAHL、Wiley Cochrane图书馆、Scopus、Clinicaltrials.gov和WHO国际临床试验注册平台(ICTRP)上进行了系统检索。纳入了2000年及以后发表的所有评估益生菌用于0至10岁儿童急性和持续性腹泻管理的研究。使用Cochrane偏倚风险II(RoB - 2)工具评估偏倚风险,并使用推荐分级、评估、制定和评价(GRADE)方法评估证据质量。本评价由WHO委托进行,以修订其儿童腹泻管理指南。
该评价纳入了98项研究,共17236名参与者。研究根据WHO腹泻定义或作者指定的定义进行分类。在考虑WHO腹泻定义的研究中,与急性腹泻儿童的对照组相比,益生菌组更有可能实现临床治愈(风险比 = 1.12(95%置信区间(CI)= 1.01,1.24,研究 = 14))并缩短腹泻持续时间(平均差 = -13.27小时(95% CI = -16.72,-9.83,研究 = 33))。然而,效应量较小,统计异质性非常高,导致证据的确定性较低。在持续性腹泻儿童中,益生菌使腹泻持续时间缩短了95小时(平均差 = -96.45(95% CI = -110.53,-82.37,研究 = 2)),但证据的确定性非常低。
该系统评价的结果表明,关于益生菌对儿童临床治愈和腹泻持续时间影响的证据确定性较低。试验和给药中益生菌的属、种、剂量和治疗持续时间存在显著差异。高水平的异质性降低了证据的确定性。需要进行大规模随机临床试验来评估特定的益生菌菌株和剂量。此外,未来研究需要探索成本效益分析研究。
本评价方案已在国际前瞻性系统评价注册库(PROSPERO:CRD42023449200)注册。