Nakai Chie, Miwa Kosei, Kitagawa Yasuhide, Kikuchi Moemi, Namiki Sanae, Kikuchi Mina, Kawase Kota, Iinuma Koji, Tobisawa Yuki, Nakane Keita, Koie Takuya
Department of Urogynecology, Japanese Red Cross Gifu Hospital, Gifu 5028511, Japan.
Department of Urology, Komatsu Municipal Hospital, Komatsu 9238560, Japan.
J Clin Med. 2025 Jun 11;14(12):4151. doi: 10.3390/jcm14124151.
Intradetrusor botulinum toxin injection is a well-established third-line therapy for patients with refractory overactive bladder (OAB) and detrusor overactivity (DO). Botulinum toxin type A (BoNT-A) is most commonly used due to its prolonged therapeutic duration. We aimed to evaluate the effectiveness of intradetrusor BoNT-A injection therapy in managing refractory OAB by performing a urodynamic study (UDS). : The patients were prospectively enrolled between February 2020 and March 2021. The patients received treatment regimens comprising behavioral modification therapy, pelvic floor muscle physiotherapy, and/or OAB medications for at least three months. The UDS procedure was carried out by a single examiner, in accordance with the International Continence Society standards for good urodynamic practice. A total of 100 units of BoNT-A was dissolved in 10 mL of saline, and 0.5 mL (5 units) was injected at 20 sites on the posterior wall of the bladder. The primary endpoint was the change in DO, which was measured using the UDS from the baseline to two months after treatment with BoNT-A. : Prior to treatment initiation, DO was observed in all the patients during the UDS. The occurrence of DO during the filling phase demonstrated a significant decrease following treatment, with DO no longer identified in 27.3% of the patients. The first sensation of bladder filling, maximum cystometric capacity, DO, and terminal DO all demonstrated significant improvement after intradetrusor BoNT-A injection, based on the UDS. The OAB symptom scores also significantly decreased after BoNT-A therapy. : The present study demonstrated that intradetrusor BoNT-A injection significantly improved symptoms in patients with OAB who had been unresponsive to various treatments. This study also demonstrated the usefulness of performing a UDS before and after treatment to prove the efficacy of BoNT-A.
膀胱逼尿肌内注射肉毒杆菌毒素是治疗难治性膀胱过度活动症(OAB)和逼尿肌过度活动(DO)患者的一种成熟的三线治疗方法。由于A型肉毒杆菌毒素(BoNT-A)的治疗持续时间较长,因此最为常用。我们旨在通过进行尿动力学研究(UDS)来评估膀胱逼尿肌内注射BoNT-A治疗难治性OAB的有效性。:患者于2020年2月至2021年3月前瞻性入组。患者接受了包括行为矫正治疗、盆底肌物理治疗和/或OAB药物治疗在内的治疗方案,为期至少三个月。UDS程序由一名检查者按照国际尿控协会良好尿动力学实践标准进行。将总共100单位的BoNT-A溶解在10 mL生理盐水中,在膀胱后壁的20个部位注射0.5 mL(5单位)。主要终点是DO的变化,通过UDS从基线测量至BoNT-A治疗后两个月。:在开始治疗前,所有患者在UDS期间均观察到DO。充盈期DO的发生率在治疗后显著降低,27.3%的患者未再检测到DO。基于UDS,膀胱充盈的首次感觉、最大膀胱测压容量、DO和终末DO在膀胱逼尿肌内注射BoNT-A后均有显著改善。BoNT-A治疗后OAB症状评分也显著降低。:本研究表明,膀胱逼尿肌内注射BoNT-A可显著改善对各种治疗无反应的OAB患者的症状。本研究还证明了在治疗前后进行UDS以证明BoNT-A疗效的有用性。