Empitu Maulana, Jayanthi Ruthvika, Yasin Muhammad Nabhan, Bouqoufi Afaf
Faculty of Medicine, Airlangga University, Surabaya, East Java, Indonesia
Faculty of Health, Medicine, and Natural Sciences, Airlangga University, Banyuwangi, East Java, Indonesia.
BMJ Open. 2025 May 14;15(5):e100159. doi: 10.1136/bmjopen-2025-100159.
Atypical Haemolytic Uremic Syndrome (aHUS) is a rare but life-threatening thrombotic microangiopathy. If inadequately managed, aHUS can lead to progressive kidney failure, cardiovascular complications and multiorgan dysfunction, resulting in high healthcare costs and a substantial impact on patients' quality of life. Novel complement inhibitors offer potential advantages, yet comprehensive evidence comparing their efficacy and safety is limited. This protocol elaborates the systematic review plans to evaluate the effectiveness and the drug safety of complement inhibitors in aHUS.
A systematic search will be conducted across PubMed, Embase, Cochrane Library, Web of Science and Scopus to identify relevant studies. Eligible studies include randomised controlled trials (RCTs), observational studies and case series with at least three aHUS patients treated with novel complement inhibitors. Two independent reviewers will perform data extraction and quality assessment using standardised tools, including the Risk of Bias Tool 2 for RCTs and the Newcastle-Ottawa Scale for observational studies. A meta-analysis will be conducted if feasible, utilising a random-effects model to account for study heterogeneity.
Ethical approval is not required as only previously published data will be used. Results will be disseminated via peer-reviewed journals and conferences, targeting healthcare professionals and policymakers to support evidence-based decision-making in aHUS management.
CRD42025629879.
非典型溶血性尿毒症综合征(aHUS)是一种罕见但危及生命的血栓性微血管病。如果管理不当,aHUS可导致进行性肾衰竭、心血管并发症和多器官功能障碍,从而导致高昂的医疗费用,并对患者的生活质量产生重大影响。新型补体抑制剂具有潜在优势,但比较其疗效和安全性的全面证据有限。本方案详细阐述了系统评价计划,以评估补体抑制剂在aHUS中的有效性和药物安全性。
将在PubMed、Embase、Cochrane图书馆、Web of Science和Scopus上进行系统检索,以识别相关研究。符合条件的研究包括随机对照试验(RCT)、观察性研究和病例系列,其中至少有三名aHUS患者接受新型补体抑制剂治疗。两名独立的评审员将使用标准化工具进行数据提取和质量评估,包括用于RCT的偏倚风险工具2和用于观察性研究的纽卡斯尔-渥太华量表。如果可行,将进行荟萃分析,使用随机效应模型来考虑研究的异质性。
由于仅使用以前发表的数据,因此无需伦理批准。研究结果将通过同行评审期刊和会议进行传播,目标受众为医疗保健专业人员和政策制定者,以支持aHUS管理中的循证决策。
PROSPERO注册号:CRD42025629879。