Department of Urology, Eberhard-Karls-University, Hoppe-Seyler-Street 3, 72076, Tübingen, Germany.
World J Urol. 2012 Jun;30(3):367-73. doi: 10.1007/s00345-011-0736-6. Epub 2011 Aug 13.
To document the videourodynamic changes and the efficacy and safety profile of botulinum toxin A (BoNT-A, Dysport(®)) in neurogenic bladder dysfunction (NBD) including neurogenic detrusor overactivity, low-compliance and break-low-compliance and idiopathic detrusor overactivity (IDO), in patients refractory to drug treatment.
Sixty-four patients with NBD and 170 patients with IDO were treated between 2002 and 2007. Diagnostic approach included medical history, bladder diary, standardised questionnaire rating quality of life, sonography, videourodynamic and temporary sacral nerve block. All patients received BoNT-A-injection under local anaesthesia. Patients with NBD received 500 mouse units (MU) and patients with IDO received 250 MU BoNT-A, injected into ten sites including the trigonum. Patients were followed up 6 weeks after injection.
For NBD, 58/64 (91%) patients achieved satisfactory continence during the day as well as significant reduction in incontinence episodes and improvement in quality of life. For IDO, 158/170 (93%) were responders with regard to urgency and urge incontinence. Urodynamical changes included significant improvement in the following parameters in both groups: increase in maximum cystometric capacity and decrease in detrusor pressure. BoNT-A was well tolerated; no drug-related side effects were documented. No de novo vesicoureteral reflux was induced. Long-term follow-up revealed a mean duration effect of BoNT-A of 5.7 months in NBD and 4.9 months in IDO.
BoNT-A is highly effective in NBD as well as in IDO suggesting that this is a good treatment option for patients with detrusor overactivity. Furthermore, intratrigonal injection is safe and not associated with vesicoureteral reflux.
记录神经原性膀胱功能障碍(NBD)患者(包括神经原性逼尿肌过度活动、顺应性低和低顺应性膀胱破裂、特发性逼尿肌过度活动(IDO))接受肉毒毒素 A(BoNT-A,Dysport®)治疗后的尿动力学变化、疗效和安全性。
2002 年至 2007 年间,64 名 NBD 患者和 170 名 IDO 患者接受了治疗。诊断方法包括病史、膀胱日记、标准化问卷评估生活质量、超声检查、尿动力学和临时骶神经阻滞。所有患者均在局部麻醉下接受 BoNT-A 注射。NBD 患者接受 500 个小鼠单位(MU),IDO 患者接受 250 MU BoNT-A,注射到十个部位,包括三角区。患者在注射后 6 周进行随访。
对于 NBD,58/64(91%)名患者白天达到满意的控尿,失禁发作次数显著减少,生活质量得到改善。对于 IDO,158/170(93%)名患者对尿急和急迫性尿失禁有反应。尿动力学变化包括两组患者以下参数的显著改善:最大膀胱容量增加,逼尿肌压力降低。BoNT-A 耐受性良好;无药物相关副作用。未诱发新的膀胱输尿管反流。长期随访显示,BoNT-A 在 NBD 中的平均持续作用时间为 5.7 个月,在 IDO 中的平均持续作用时间为 4.9 个月。
BoNT-A 对 NBD 和 IDO 均有效,表明这是治疗逼尿肌过度活动患者的一种较好的治疗选择。此外,三角区注射是安全的,不会引起膀胱输尿管反流。