Efficacy and safety of Optilume® paclitaxel-coated urethral dilatation balloon in real-life: experience in a Spanish multicenter study

C. Ballesteros Ruiz , F. Campos-Juanatey , I. Povo Martín , S. Mitjana Biosca , Ó. Gorría Cardesa , J.F. Aguilar Guevara , N. García Formoso , E. Fernández Pascual , J.I. Martínez Salamanca , S. Martínez Pérez , J.M. Alonso Dorrego , E. Ríos González , S. San Cayetano Talegón , A.M. Araujo Suarez , E. Moran Pascual , M.Á. Bonillo García , J. Medina Polo , L. Viver Clotet , A.J. Vicens Morton , J. Arce Gil , L. Martínez-Piñeiro Lorenzo
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Abstract

Introduction

The Optilume® Paclitaxel-coated urethral dilatation balloon is an alternative to conventional endoscopic treatments that combines mechanical dilatation with local delivery of paclitaxel.

Objective

To describe the success rate and analyze the safety of the device in real clinical practice. To evaluate possible predictors of treatment failure.

Materials and methods

Retrospective multicenter study in patients diagnosed with urethral stricture and treated with an Optilume® balloon in routine clinical practice. Data were collected from flowmetry, questionnaires (PROM and IPSS) and cystoscopy before surgery, and 3, 6 and 12 months after the procedure, according to standard practice. Surgical success was defined as the absence of subsequent urethral manipulation and a Qmax >10 ml/s.

Results

238 patients treated with Optilume® in 12 Spanish hospitals between May 2021 and April 2024 were included in the study. Of these, 156 who had a minimum follow-up of 3 months, were analyzed. Median stricture length: 1.5 cm (0.5–5.3), mainly in bulbar urethra (87.7%). Of the total, 12.8% of patients had a history of pelvic radiotherapy, and 81.4% had undergone prior urethral manipulation. Postoperative complications were reported in 14.2% of the total. The treatment success rate was 73.8%, with a median follow-up of 8 months (5–12). No predictors of stricture recurrence were identified. Recurrence rates were higher in strictures located in the posterior versus anterior urethra (42.9% vs. 24.6%, p = 0.126). No significant differences were observed between patients with and without prior urethral manipulation.

Conclusion

Treatment with Optilume® has been shown to be safe and effective in short-term routine clinical practice.
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Optilume® 紫杉醇涂层尿道扩张球囊在现实生活中的有效性和安全性:西班牙多中心研究的经验。
简介:Optilume® 紫杉醇涂层尿道扩张球囊是传统内窥镜治疗的替代方法,它将机械扩张与紫杉醇局部给药相结合:描述该设备在实际临床实践中的成功率并分析其安全性。评估治疗失败的可能预测因素:回顾性多中心研究,对象是在常规临床实践中被诊断为尿道狭窄并接受 Optilume® 球囊治疗的患者。按照标准做法,在术前、术后 3 个月、6 个月和 12 个月通过流量计、问卷调查(PROM 和 IPSS)和膀胱镜检查收集数据。手术成功的定义是没有后续的尿道操作,Qmax > 10 ml/s。结果:2021 年 5 月至 2024 年 4 月期间,在西班牙 12 家医院接受 Optilume® 治疗的 238 名患者被纳入研究。对其中至少随访 3 个月的 156 名患者进行了分析。中位狭窄长度:1.5 厘米(0.5 - 5.3),主要位于球部尿道(87.7%)。其中,12.8%的患者曾接受过盆腔放疗,81.4%的患者曾接受过尿道操作。据报告,14.2%的患者出现了术后并发症。治疗成功率为 73.8%,中位随访时间为 8 个月(5-12 个月)。没有发现狭窄复发的预测因素。位于后尿道的狭窄复发率高于前尿道(42.9% 对 24.6%,P = 0.126)。结论:使用 Optilume® 治疗尿道狭窄的效果良好:结论:在短期常规临床实践中,使用 Optilume® 治疗已被证明是安全有效的。
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