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口服抗胆碱能药物与安慰剂或不治疗成人膀胱过度活动症。

Oral anticholinergic drugs versus placebo or no treatment for managing overactive bladder syndrome in adults.

机构信息

Evidence Synthesis Group, Population Health Sciences Institute, Newcastle University, Newcastle upon Tyne, UK.

Obstetrics & Gynaecology, Sheffield Teaching Hospital NHS Foundation Trust, Sheffield, UK.

出版信息

Cochrane Database Syst Rev. 2023 May 9;5(5):CD003781. doi: 10.1002/14651858.CD003781.pub3.

Abstract

BACKGROUND

Around 16% of adults have symptoms of overactive bladder (OAB; urgency with frequency and/or urge incontinence), with prevalence increasing with age. Anticholinergic drugs are commonly used to treat this condition. This is an update of a Cochrane Review first published in 2002 and last updated in 2006.

OBJECTIVES

To assess the effects of anticholinergic drugs compared with placebo or no treatment for treating overactive bladder syndrome in adults.

SEARCH METHODS

We searched the Cochrane Incontinence Specialised Register, which contains trials identified from the Cochrane Central Register of Controlled Trials (CENTRAL), MEDLINE, MEDLINE In-Process, MEDLINE Epub Ahead of Print, ClinicalTrials.gov, WHO ICTRP and handsearching of journals and conference proceedings (searched 14 January 2020), and the reference lists of relevant articles. We updated this search on 3 May 2022, but these results have not yet been fully incorporated.

SELECTION CRITERIA

We included randomised or quasi-randomised trials in adults with overactive bladder syndrome that compared an anticholinergic drug alone with placebo treatment.

DATA COLLECTION AND ANALYSIS

Two review authors independently assessed eligibility and extracted data from the included studies, including an assessment of the risk of bias. We assessed the certainty of the body of evidence using the GRADE approach. We processed data as described in the Cochrane Handbook for Systematic Reviews of Interventions.

MAIN RESULTS

We included 104 studies, 71 of which were new or updated for this version of the review. Although 12 studies did not report the number of participants, there were 47,106 people in the remainder of the included studies. The majority of the studies had insufficient information to allow judgement of risk of bias and we judged them to be unclear for all domains. Nine anticholinergic drugs were included in these studies: darifenacin; fesoterodine; imidafenacin; oxybutynin; propantheline; propiverine; solifenacin; tolterodine and trospium. No studies were found that compared anticholinergic drugs to no treatment. At the end of the treatment period, anticholinergics may slightly increase condition-specific quality of life (mean difference (MD) 4.41 lower, 95% confidence interval (CI) 5.28 lower to 3.54 lower (scale range -100 to 0); 12 studies, 6804 participants; low-certainty evidence). Anticholinergics are probably better than placebo in terms of patient perception of cure or improvement (risk ratio (RR) 1.38, 95% CI 1.15 to 1.66; 9 studies, 8457 participants; moderate-certainty evidence), and the mean number of urgency episodes per 24-hour period (MD 0.85 lower, 95% CI 1.03 lower to 0.67 lower; 23 studies, 16,875 participants; moderate-certainty evidence). Compared to placebo, anticholinergics may result in an increase in dry mouth adverse events (RR 3.50, 95% CI 3.26 to 3.75; 66 studies, 38,368 participants; low-certainty evidence), and may result in an increased risk of urinary retention (RR 3.52, 95% CI 2.04 to 6.08; 17 studies, 7862 participants; low-certainty evidence). Taking anticholinergics may be more likely to lead to participants withdrawing from the studies due to adverse events (RR 1.37, 95% CI 1.21 to 1.56; 61 studies, 36,943 participants; low-certainty evidence). However, taking anticholinergics probably reduces the mean number of micturitions per 24-hour period compared to placebo (MD 0.85 lower, 95% CI 0.98 lower to 0.73 lower; 30 studies, 19,395 participants; moderate-certainty evidence).

AUTHORS' CONCLUSIONS: The use of anticholinergic drugs by people with overactive bladder syndrome results in important but modest improvements in symptoms compared with placebo treatment. In addition, recent studies suggest that this is generally associated with only modest improvement in quality of life. Adverse effects were higher with all anticholinergics compared with placebo. Withdrawals due to adverse effects were also higher for all anticholinergics except tolterodine. It is not known whether any benefits of anticholinergics are sustained during long-term treatment or after treatment stops.

摘要

背景

大约 16%的成年人有膀胱过度活动症(OAB;伴有频率和/或急迫性尿失禁的尿急)的症状,患病率随年龄增长而增加。抗胆碱能药物常用于治疗这种疾病。这是对 Cochrane 综述的更新,该综述首次发表于 2002 年,最后一次更新于 2006 年。

目的

评估抗胆碱能药物与安慰剂或不治疗成人膀胱过度活动症的疗效。

检索方法

我们检索了 Cochrane 尿控专题注册库,其中包含从 Cochrane 对照试验中心注册库(CENTRAL)、MEDLINE、MEDLINE 正在处理、MEDLINE Epub 提前获取、ClinicalTrials.gov、世界卫生组织国际临床试验注册平台和期刊会议论文集(2020 年 1 月 14 日检索)手工检索的试验,以及相关文章的参考文献列表。我们于 2022 年 5 月 3 日更新了这次检索,但这些结果尚未完全纳入。

选择标准

我们纳入了在膀胱过度活动症成年人中比较抗胆碱能药物与安慰剂治疗的随机或准随机试验。

数据收集和分析

两位综述作者独立评估纳入研究的资格并提取数据,包括对偏倚风险的评估。我们使用 GRADE 方法评估证据的确定性。我们按照 Cochrane 干预措施系统评价手册中的描述处理数据。

主要结果

我们纳入了 104 项研究,其中 71 项是为本次更新而新增或更新的。尽管有 12 项研究未报告参与者的数量,但其余研究中仍有 47,106 人。大多数研究信息不足,无法判断偏倚风险,我们对所有领域均判断为不清楚。9 种抗胆碱能药物包括:达非那新、非索罗定、依美沙嗪、奥昔布宁、普罗潘酮、丙哌维林、索利那新、托特罗定和曲司氯铵。没有研究比较抗胆碱能药物与不治疗。在治疗期末,抗胆碱能药物可能会略微提高特定于疾病的生活质量(平均差值 4.41,95%置信区间 5.28 至 3.54;12 项研究,6804 名参与者;低确定性证据)。抗胆碱能药物在患者对治愈或改善的感知方面可能优于安慰剂(风险比 1.38,95%置信区间 1.15 至 1.66;9 项研究,8457 名参与者;中等确定性证据),并且每 24 小时急迫性发作次数平均减少 0.85(95%置信区间 1.03 至 0.67;23 项研究,16875 名参与者;中等确定性证据)。与安慰剂相比,抗胆碱能药物可能会增加口干不良反应的风险(相对风险 3.50,95%置信区间 3.26 至 3.75;66 项研究,38368 名参与者;低确定性证据),并可能增加尿潴留的风险(相对风险 3.52,95%置信区间 2.04 至 6.08;17 项研究,7862 名参与者;低确定性证据)。与安慰剂相比,使用抗胆碱能药物可能会导致更多的参与者因不良反应而退出研究(相对风险 1.37,95%置信区间 1.21 至 1.56;61 项研究,36943 名参与者;低确定性证据)。然而,与安慰剂相比,抗胆碱能药物可能会使每 24 小时排尿次数平均减少 0.85(95%置信区间 0.98 至 0.73;30 项研究,19395 名参与者;中等确定性证据)。

作者结论

与安慰剂相比,膀胱过度活动症患者使用抗胆碱能药物治疗可显著改善症状,但改善幅度适中。此外,最近的研究表明,这通常与生活质量的适度改善有关。与安慰剂相比,所有抗胆碱能药物的不良反应都更高。除了托特罗定外,所有抗胆碱能药物的不良反应导致的退出率也更高。抗胆碱能药物在长期治疗或治疗停止后的疗效是否持续尚不清楚。

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