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本文引用的文献

1
or resolved urgency and urgency urinary incontinence after midurethral sling operations: How can we properly counsel our patients?经尿道中段吊带术后急迫性尿失禁或急迫性尿失禁缓解:我们应如何正确为患者提供咨询?
Investig Clin Urol. 2019 Sep;60(5):373-379. doi: 10.4111/icu.2019.60.5.373. Epub 2019 Aug 8.
2
Fundamentals of terminology in lower urinary tract function.下尿路功能术语基础。
Neurourol Urodyn. 2018 Aug;37(S6):S13-S19. doi: 10.1002/nau.23768.
3
Urinary Incontinence in Women: A Review.女性尿失禁:综述。
JAMA. 2017 Oct 24;318(16):1592-1604. doi: 10.1001/jama.2017.12137.
4
Can incontinence be cured? A systematic review of cure rates.大小便失禁能治愈吗?治愈率的系统评价。
BMC Med. 2017 Mar 24;15(1):63. doi: 10.1186/s12916-017-0828-2.
5
Midurethral slings: evidence-based medicine vs the medicolegal system.尿道中段吊带:循证医学与医疗法律体系。
Am J Obstet Gynecol. 2016 Jun;214(6):708.e1-5. doi: 10.1016/j.ajog.2016.04.018. Epub 2016 Apr 19.
6
Mirabegron as Add-On Treatment to Solifenacin in Patients with Incontinent Overactive Bladder and an Inadequate Response to Solifenacin Monotherapy: Responder Analyses and Patient-Reported Outcomes from the BESIDE Study [corrected].米拉贝隆作为索利那新单药治疗无效的膀胱过度活动症伴尿急患者的附加治疗:BESIDE 研究的应答者分析和患者报告结局[更正]。
J Urol. 2016 Sep;196(3):809-18. doi: 10.1016/j.juro.2016.03.174. Epub 2016 Apr 8.
7
Efficacy and Safety of Mirabegron Add-on Therapy to Solifenacin in Incontinent Overactive Bladder Patients with an Inadequate Response to Initial 4-Week Solifenacin Monotherapy: A Randomised Double-blind Multicentre Phase 3B Study (BESIDE).米拉贝隆附加治疗对初始 4 周索利那新单药治疗反应不足的失禁型逼尿过度活动症患者的疗效和安全性:一项随机双盲多中心 3B 期研究(BESIDE)。
Eur Urol. 2016 Jul;70(1):136-145. doi: 10.1016/j.eururo.2016.02.030. Epub 2016 Mar 8.
8
The safety and efficiency of onabotulinumtoxinA for the treatment of overactive bladder: a systematic review and meta-analysis.A型肉毒毒素治疗膀胱过度活动症的安全性和有效性:一项系统评价与荟萃分析
Int Urol Nephrol. 2015 Nov;47(11):1779-88. doi: 10.1007/s11255-015-1125-7. Epub 2015 Oct 3.
9
Female urinary stress incontinence.女性压力性尿失禁
Climacteric. 2015;18 Suppl 1:30-6. doi: 10.3109/13697137.2015.1090859.
10
Mid-urethral sling operations for stress urinary incontinence in women.女性压力性尿失禁的中段尿道吊带手术
Cochrane Database Syst Rev. 2015 Jul 1(7):CD006375. doi: 10.1002/14651858.CD006375.pub3.

一项评估肉毒毒素 A 注射联合中尿道吊带术治疗尿失禁患者疗效的对照观察性研究。

A Comparative Observational Study to Evaluate the Efficacy of Mid-Urethral Sling with Botulinum Toxin A Injection in Urinary Incontinence Patients.

机构信息

Department of Urology, China Medical University Hospital, Taichung 40447, Taiwan.

School of Medicine, China Medical University, Taichung 40402, Taiwan.

出版信息

Toxins (Basel). 2020 Jun 2;12(6):365. doi: 10.3390/toxins12060365.

DOI:10.3390/toxins12060365
PMID:32498306
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7354459/
Abstract

This study aimed to evaluate and compare the efficacy and safety of mid-urethral sling (MUS) with botulinum toxin A (BoNT-A) versus MUS only in women with mixed urinary incontinence. This was a comparative observational study, and total of 73 patients were enrolled. A total of 38 and 35 patients received MUS only and MUS with BoNT-A injection, respectively. The efficacy outcome included change in Urinary Incontinence Outcome Scores (UIOS), change in Overactive Bladder Symptom Score (OABSS), and use of antimuscarinic agent or beta-3 agonist. Safety assessments included adverse events including urinary retention, increased postvoid residual volumes, and urinary tract infection. MUS with BoNT-A injection was insignificantly better than MUS only in urinary incontinence outcome (88% vs. 71%, respectively, = 0.085) at week three. Among the 33 patients with detrusor overactivity (DO), patients who received BoNT-A had a higher cure rate of incontinence (88% vs. 41%, = 0.01) and less required antimuscarinic agent or beta-3 agonist (31% vs. 94%, < 0.001) compared to patients who did not receive BoNT-A injection. There was no significant difference in the incidences of adverse events between two groups. BoNT-A injection with MUS demonstrated efficacy and safety in the treatment of mixed urinary incontinence, specifically for women with DO.

摘要

本研究旨在评估和比较中尿道吊带(MUS)联合肉毒毒素 A(BoNT-A)与单独 MUS 在混合性尿失禁女性中的疗效和安全性。这是一项比较观察性研究,共纳入 73 例患者。共有 38 例和 35 例患者分别接受了单独的 MUS 和 MUS 联合 BoNT-A 注射治疗。疗效结局包括尿失禁结局评分(UIOS)的变化、膀胱过度活动症症状评分(OABSS)的变化以及抗毒蕈碱药物或 β3 激动剂的使用。安全性评估包括包括尿潴留、残余尿量增加和尿路感染等不良事件。在第 3 周时,MUS 联合 BoNT-A 注射在尿失禁结局方面略优于单独使用 MUS(分别为 88%和 71%, = 0.085)。在 33 例逼尿肌过度活动(DO)患者中,接受 BoNT-A 治疗的患者失禁治愈率更高(88%比 41%, = 0.01),需要抗毒蕈碱药物或 β3 激动剂的比例更低(31%比 94%, < 0.001),与未接受 BoNT-A 注射的患者相比。两组不良事件的发生率无显著差异。MUS 联合 BoNT-A 注射在治疗混合性尿失禁方面具有疗效和安全性,特别是对 DO 女性。