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肉毒杆菌毒素在神经泌尿学中的应用。

Botulinum Toxin Use in Neurourology.

作者信息

Peyronnet Benoit, Gamé Xavier, Vurture Gregory, Nitti Victor W, Brucker Benjamin M

机构信息

Department of Urology, University of Rennes Rennes, France.

Department of Urology, New York University New York, NY.

出版信息

Rev Urol. 2018;20(2):84-93. doi: 10.3903/riu0792.

DOI:10.3903/riu0792
PMID:30288145
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6168325/
Abstract

The use of botulinum toxin A (BTX-A) has revolutionized the treatment of neurogenic lower urinary tract dysfunction (NLUTD) over the past three decades. Initially, it was used as a sphincteric injection for detrusor sphincter dyssynergia but now is used mostly as intradetrusor injection to treat neurogenic detrusor overactivity (NDO). Its use is supported by high-level-of-evidence studies and it has become the gold-standard treatment for patients with NDO refractory to anticholinergics. Several novelties have emerged in the use of BTX-A in neurourology over the past few years. Although onabotulinumtoxinA (BOTOX, Allergan, Inc., Irvine, CA) remains the only BTX-A for which use is supported by large, multicenter, randomized, controlled trials (RCT), and is therefore the only one to be licensed in the United States and Europe, a second BTX-A, abobotulinumtoxinA (Dysport, Ipsen Biopharmaceuticals, Basking Ridge, NJ), is also supported by high-level-of-evidence studies. Other innovations in the use of BTX-A in neurourology during the past few years include the BTX switch (from abobotulinumtoxinA to onabotulinumtoxinA or the opposite) as a rescue option for primary or secondary failures of intradetrusor BTX-A injection and refinements in intradetrusor injection techniques (number of injection sites, injection into the trigone). There is also a growing interest in long-term failure of BTX-A for NDO and their management, and a possible new indication for urethral sphincter injections.

摘要

在过去三十年里,肉毒杆菌毒素A(BTX-A)的使用彻底改变了神经源性下尿路功能障碍(NLUTD)的治疗方式。最初,它被用作治疗逼尿肌括约肌协同失调的括约肌注射药物,但现在主要用作膀胱逼尿肌内注射来治疗神经源性逼尿肌过度活动(NDO)。其应用得到了高证据水平研究的支持,并且已成为抗胆碱能药物治疗无效的NDO患者的金标准治疗方法。在过去几年中,BTX-A在神经泌尿学中的应用出现了一些新进展。尽管注射用A型肉毒毒素(保妥适,艾尔建公司,加利福尼亚州欧文市)仍然是唯一一种得到大型、多中心、随机、对照试验(RCT)支持其使用的BTX-A,因此也是在美国和欧洲唯一获得许可的一种,但另一种BTX-A,即A型肉毒杆菌毒素(达力士,益普生生物制药公司,新泽西州巴斯金里奇),也得到了高证据水平研究的支持。过去几年中,BTX-A在神经泌尿学应用中的其他创新包括BTX转换(从A型肉毒杆菌毒素转换为注射用A型肉毒毒素或相反),作为膀胱逼尿肌内BTX-A注射原发性或继发性失败的挽救选择,以及膀胱逼尿肌内注射技术的改进(注射部位数量、三角区注射)。人们对BTX-A治疗NDO的长期失败及其管理也越来越感兴趣,并且尿道括约肌注射可能有新的适应证。

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本文引用的文献

1
[Efficacy of botulinum toxin A injections in the urethral sphincter in patients with difficulties to perform self-intermittent catherization].A型肉毒杆菌毒素注射尿道括约肌对自我间歇性导尿困难患者的疗效
Prog Urol. 2018 Jun;28(7):370-376. doi: 10.1016/j.purol.2018.04.001.
2
Failures and long-term discontinuations of intradetrusor botulinum toxin injections for neurogenic detrusor overactivity: A new challenge in neurourology.用于神经源性逼尿肌过度活动的膀胱逼尿肌内注射肉毒杆菌毒素的失败及长期停药:神经泌尿学中的一项新挑战。
Neurourol Urodyn. 2018 Mar;37(3):1182-1183. doi: 10.1002/nau.23424. Epub 2017 Oct 9.
3
Is repeat Botulinum Toxin A injection valuable for neurogenic detrusor overactivity-A systematic review and meta-analysis.重复注射肉毒毒素 A 治疗神经原性逼尿肌过度活动症是否有价值——系统评价和荟萃分析。
Neurourol Urodyn. 2018 Feb;37(2):542-553. doi: 10.1002/nau.23354. Epub 2017 Jul 26.
4
Long-term outcomes and risks factors for failure of intradetrusor onabotulinumtoxin A injections for the treatment of refractory neurogenic detrusor overactivity.膀胱内注射A型肉毒毒素治疗难治性神经源性逼尿肌过度活动的长期疗效及失败风险因素
Neurourol Urodyn. 2018 Feb;37(2):799-806. doi: 10.1002/nau.23352. Epub 2017 Jul 26.
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Disease-Specific Outcomes of Botulinum Toxin Injections for Neurogenic Detrusor Overactivity.肉毒杆菌毒素注射治疗神经源性逼尿肌过度活动的疾病特异性结局
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Neurourol Urodyn. 2018 Jan;37(1):291-297. doi: 10.1002/nau.23291. Epub 2017 Apr 21.
8
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Neurourol Urodyn. 2017 Apr;36(4):1104-1107. doi: 10.1002/nau.23052. Epub 2016 Jun 10.
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Neurourol Urodyn. 2017 Mar;36(3):557-564. doi: 10.1002/nau.23025. Epub 2016 May 17.
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Botulinum Toxin A and Lower Urinary Tract Dysfunction: Pathophysiology and Mechanisms of Action.A型肉毒毒素与下尿路功能障碍:病理生理学及作用机制
Toxins (Basel). 2016 Apr 21;8(4):120. doi: 10.3390/toxins8040120.