Seth J H, Dowson C, Khan M S, Panicker J N, Fowler C J, Dasgupta P, Sahai A
Department of Uro-Neurology, National Hospital for Neurology and Neurosurgery, UCL Hospitals Foundation Trust, UK.
Department of Urology, Medical Research Council (MRC) Centre for Transplantation and Guy's and St Thomas' NHS Trust, King's College London, King's Health Partners, Guy's Hospital, UK.
J Clin Urol. 2013 Mar;6(2):77-83. doi: 10.1177/2051415812473096.
Botulinum toxin-A (BoNT/A) is now established second-line management for refractory overactive bladder (OAB) and recognised in many incontinence guidelines and pathways. For those with neurogenic detrusor overactivity secondary to spinal cord injury or multiple sclerosis, the toxin is currently licensed in certain parts of the world, including the UK. It is an effective treatment in those in whom antimuscarinics and conservative measures have failed who have symptoms of OAB and or detrusor overactivity (DO).
Treatment can be given in an outpatient setting and can be administered under local anaesthesia. Its efficacy lasts for between six and 12 months.
It has an acceptable safety profile with the biggest risk being urinary tract infection and difficulty emptying the bladder, necessitating clean intermittent self-catheterisation (CISC). Medium-term follow-up suggests repeated injections are also safe and efficacious.
The mechanism of action of the toxin is more complicated than originally thought, and it seems likely that it affects motor and sensory nerves of the bladder. In the last 10 years much of the progress of this treatment from early experimental trials to mainstream clinical use, and a better understanding of how it works in the bladder, are as a result of research conducted in the UK. This review summarises the significant and substantial evidence for BoNT/A to treat refractory OAB from UK centres.
肉毒杆菌毒素A(BoNT/A)现已成为难治性膀胱过度活动症(OAB)的二线治疗方法,并在许多尿失禁指南和治疗路径中得到认可。对于继发于脊髓损伤或多发性硬化症的神经源性逼尿肌过度活动患者,该毒素目前在世界某些地区(包括英国)已获许可使用。对于抗毒蕈碱药物治疗和保守治疗均无效且出现OAB症状和/或逼尿肌过度活动(DO)的患者,它是一种有效的治疗方法。
治疗可在门诊进行,且可在局部麻醉下给药。其疗效可持续6至12个月。
它具有可接受的安全性,最大风险是尿路感染和膀胱排空困难,这需要进行清洁间歇性自我导尿(CISC)。中期随访表明重复注射也是安全有效的。
该毒素的作用机制比最初认为的更为复杂,似乎它会影响膀胱的运动神经和感觉神经。在过去10年中,这种治疗方法从早期实验性试验发展到主流临床应用,并对其在膀胱中的作用方式有了更好的理解,这都归功于英国开展的研究。本综述总结了来自英国各中心关于BoNT/A治疗难治性OAB的重要且充分的证据。