van Veen Felice E E, Schotman Martje, 't Hoen Lisette A, Blok Bertil F M, Scheepe Jeroen R
Department of Urology and Pediatric Urology, Sophia Children's Hospital, Erasmus MC, Rotterdam, the Netherlands.
Department of Urology and Pediatric Urology, Sophia Children's Hospital, Erasmus MC, Rotterdam, the Netherlands.
J Pediatr Urol. 2023 Dec;19(6):753.e1-753.e8. doi: 10.1016/j.jpurol.2023.08.015. Epub 2023 Aug 19.
Neurogenic lower urinary tract dysfunction (NLUTD) in children can cause renal failure and urinary incontinence if not treated sufficiently. Antimuscarinics (AM) and intradetrusor botulinum toxin injections (BoNT-A) with clean intermittent catheterization (CIC) are widely used treatment options for children with NLUTD. However, a considerable number will become refractory to these treatment options. This study aimed to evaluate the efficacy and long-term outcomes of mirabegron in children with NLUTD as an add-on and as a stand-alone treatment.
Patients under 18 years of age with NLUTD who were refractory to AM and/or BoNT-A and were treated with mirabegron 50 mg were retrospectively studied. Mirabegron was either used as monotherapy or in addition to AM and/or BoNT-A. Video-urodynamic studies (VUDSs) were performed before and after treatment with mirabegron. Changes in video-urodynamic parameters, the need for other NLUTD therapy during follow-up, patient-reported side effects, and urinary incontinence were outcomes of interest.
A total of 34 patients with NLUTD were included. All patients were on CIC and the median age was 13.1 years (IQR 15.9-10.3). Median follow-up was 31.4 months (IQR 57.4-11.4). Bladder compliance improved by 89.9%, from 14.9 to 28.3 ml/cm HO (p-value<0.001). Maximum cystometric capacity, end-filling detrusor pressure, volume at first detrusor overactivity, vesicoureteral reflux, and urinary incontinence significantly improved after mirabegron. The add-on therapy group showed more significant improvements in video-urodynamic outcomes compared to the monotherapy group. The median time of requiring other NLUTD therapy was 25.5 months (IQR 39.8-14.8). None of the included patients reported side effects.
Mirabegron is an effective treatment for children with therapy-refractory NLUTD with an average efficacy of 2 years after which additional therapy is required. Despite the retrospective character of this study, our results confirm the beneficial effect of mirabegron in children with therapy-refractory NLUTD, in particular when mirabegron is used as add-on therapy in those with low-compliance bladders.
儿童神经源性下尿路功能障碍(NLUTD)若未得到充分治疗,可导致肾衰竭和尿失禁。抗毒蕈碱药物(AM)、膀胱逼尿肌内注射肉毒杆菌毒素(BoNT-A)联合间歇性清洁导尿(CIC)是治疗儿童NLUTD的常用方法。然而,相当一部分患者会对这些治疗方法产生耐药性。本研究旨在评估米拉贝隆作为附加治疗和单一治疗对儿童NLUTD的疗效及长期预后。
对18岁以下难治性AM和/或BoNT-A治疗的NLUTD患者进行回顾性研究,这些患者接受50mg米拉贝隆治疗。米拉贝隆可单独使用,也可与AM和/或BoNT-A联合使用。在米拉贝隆治疗前后进行影像尿动力学检查(VUDS)。影像尿动力学参数的变化、随访期间其他NLUTD治疗的需求、患者报告的副作用以及尿失禁情况是研究的关注点。
共纳入34例NLUTD患者。所有患者均接受CIC治疗,中位年龄为13.1岁(四分位间距15.9 - 10.3)。中位随访时间为31.4个月(四分位间距57.4 - 11.4)。膀胱顺应性提高了89.9%,从14.9ml/cm H₂O提高到28.3ml/cm H₂O(p值<0.001)。米拉贝隆治疗后,最大膀胱测压容量、充盈末期逼尿肌压力、首次逼尿肌过度活动时的容量、膀胱输尿管反流和尿失禁均有显著改善。与单一治疗组相比,联合治疗组在影像尿动力学结果方面的改善更为显著。需要其他NLUTD治疗的中位时间为25.5个月(四分位间距39.8 - 14.8)。纳入的患者均未报告副作用。
米拉贝隆是治疗难治性儿童NLUTD的有效药物,平均疗效为2年,之后需要额外治疗。尽管本研究具有回顾性,但我们的结果证实了米拉贝隆对难治性儿童NLUTD的有益作用,特别是在膀胱顺应性低的患者中作为附加治疗使用时。