Protocol for a Series of Systematic Reviews and Network Meta-analyses of Randomized Controlled Trials of Medications for Patients with Overactive Bladder Symptoms

IF 3.2 3区 医学 Q1 UROLOGY & NEPHROLOGY
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Abstract

Multiple randomized controlled trials (RCTs) have examined first-line pharmacological agents such as anticholinergics and β3 agonists for the management of overactive bladder symptoms (OAB). Although earlier systematic reviews and (network) meta-analyses aimed to summarize the evidence, a substantial number of trials were not included, so a comprehensive and methodologically rigorous evaluation of the comparative effectiveness of all first-line pharmacological treatments is lacking. We aim to conduct a series of systematic reviews and network meta-analyses (NMAs) for a comprehensive assessment of the effectiveness and safety of first-line pharmacological treatments for OAB. Eligible studies will include RCTs comparing anticholinergics and β3 agonists to one another or to placebo in adults with OAB or detrusor overactivity. Pairs of reviewers with methodological training will independently evaluate candidate studies to determine eligibility and extract relevant data. We will incorporate patient-important outcomes, including urinary urgency episodes, urgency incontinence episodes, any type of incontinence episodes, urinary frequency, nocturia, and adverse events. We will conduct the NMAs using a frequentist framework and a graph theory model for each outcome. Analysis will follow rigorous methodologies, including handling of missing data and assessment of the risk of bias. We will conduct sensitivity and subgroup analyses and will apply the Grading of Recommendations Assessment, Development, and Evaluation (GRADE) approach to rate evidence certainty. Our approach aims to address the knowledge gap in the treatment of OAB by synthesizing evidence from RCTs worldwide. We will employ robust statistical methods, including frequentist NMA, to general clinically relevant and patient-important insights. Sensitivity and subgroup analyses will enhance the robustness and generalizability of our findings. Our reviews strive to inform evidence-based decisions in the management of OAB, to ultimate improve patient outcomes. Our study results may guide health policy decisions, such as reimbursement policies, and future studies in functional urology.
The protocol for the review series is registered on PROSPERO as CRD42023266915.
膀胱过度活动症患者药物治疗随机对照试验的系列系统综述和网络元分析规程
多项随机对照试验(RCT)研究了抗胆碱能药和β3受体激动剂等一线药物治疗膀胱过度活动症(OAB)的效果。尽管早期的系统综述和(网络)荟萃分析旨在总结证据,但有大量试验未被纳入,因此缺乏对所有一线药物治疗的比较效果进行全面、方法严谨的评估。我们的目标是进行一系列系统综述和网络荟萃分析(NMA),以全面评估 OAB 一线药物治疗的有效性和安全性。符合条件的研究将包括在成人 OAB 或逼尿肌过度活动患者中比较抗胆碱能药物和 β3 激动剂彼此或安慰剂的 RCT。一对受过方法学培训的评审员将独立评估候选研究,以确定是否符合条件并提取相关数据。我们将纳入患者重要的结果,包括尿急发作、尿急失禁发作、任何类型的失禁发作、尿频、夜尿和不良事件。我们将采用频数主义框架和图论模型对每种结果进行 NMA 分析。分析将遵循严格的方法,包括处理缺失数据和评估偏倚风险。我们将进行敏感性和亚组分析,并将采用建议评估、发展和评价分级法(GRADE)来评定证据的确定性。我们的方法旨在通过综合全球范围内的 RCT 证据来填补 OAB 治疗方面的知识空白。我们将采用稳健的统计方法,包括频数主义 NMA,以获得与临床相关且对患者重要的一般见解。敏感性和亚组分析将增强我们研究结果的稳健性和可推广性。我们的综述旨在为基于证据的 OAB 管理决策提供信息,以最终改善患者的治疗效果。我们的研究结果可为医疗政策决策(如报销政策)和功能性泌尿外科的未来研究提供指导。该系列综述的协议已在 PROSPERO 上注册,编号为 CRD42023266915。
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来源期刊
European Urology Open Science
European Urology Open Science UROLOGY & NEPHROLOGY-
CiteScore
3.40
自引率
4.00%
发文量
1183
审稿时长
49 days
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