Electroacupuncture Versus Pelvic Floor Muscle Training Plus Solifenacin for Women With Mixed Urinary Incontinence: A Randomized Noninferiority Trial

医学 电针 索利那新 尿失禁 随机对照试验 盆底肌 膀胱过度活动 泌尿科 盆底 针灸科 内科学 外科 病理 替代医学
作者
Baoyan Liu,Yan Liu,Zongshi Qin,Kehua Zhou,Huangfang Xu,Liyun He,Ning Li,Tongsheng Su,Jianhua Sun,Zenghui Yue,Zhiwei Zang,Wei Zhang,Jiping Zhao,Zhongyu Zhou,Lian Liu,Dongning Wu,Jiani Wu,Jing Zhou,Ran Pang,Yang Wang,Jia Liu,Jinna Yu,Zhishun Liu
出处
期刊:Mayo Clinic Proceedings [Elsevier]
卷期号:94 (1): 54-65 被引量:27
标识
DOI:10.1016/j.mayocp.2018.07.021
摘要

To evaluate the efficacy and safety of electroacupuncture vs pelvic floor muscle training (PFMT) plus solifenacin for women with mixed urinary incontinence (MUI).This randomized controlled noninferiority trial was conducted at 10 hospitals in China between March 1, 2014, and October 10, 2016. Participants were randomized 1:1 to receive electroacupuncture (36 sessions) over 12 weeks with 24 weeks of follow-up or PFMT-solifenacin (5 mg/d) over 36 weeks. The primary outcome was percentage change from baseline to week 12 in mean 72-hour incontinence episode frequency (IEF) measured by the 72-hour bladder diary. It was analyzed in the per-protocol set with a prespecified noninferiority margin of 15%.Of 500 women with MUI who were randomized, 467 (239 in the electroacupuncture group and 228 in the PFMT-solifenacin group) completed treatment per protocol and were included in the primary outcome analysis. At weeks 1 through 12, the percentage of reduction from baseline in mean 72-hour IEF was 37.83% in the electroacupuncture group and 36.49% in the PFMT-solifenacin group (between-group difference, -1.34% [95% CI, -9.78% to 7.10%]; P<.001 for noninferiority), which demonstrates noninferiority; the treatment effect persisted throughout follow-up. Statistically significant improvements were found for secondary outcomes in both groups, with no meaningful difference between treatments.In women with moderate to severe MUI, electroacupuncture was not inferior to PFMT-solifenacin in decreasing the 72-hour IEF and shows promise as an effective alternative for the treatment of MUI.clinicaltrials.gov Identifier: NCT02047032.
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