Sorbonne University, Academic Hospital Pitié-Salpétrière Paris, Paris, France.
CHU de Nantes - Hôtel Dieu, France.
Eur Urol Focus. 2021 Nov;7(6):1430-1437. doi: 10.1016/j.euf.2020.06.026. Epub 2020 Sep 7.
Real-world data that support the use of sacral neuromodulation (SNM) for lower urinary tract dysfunctions are of continued interest.
To evaluate the effectiveness, quality of life (QoL), patient-reported outcomes (PROs), and safety of SNM with the InterStim™ system in real life during 1-yr postimplant.
DESIGN, SETTING, AND PARTICIPANTS: This is a prospective, multicenter, observational study at 25 representative public and private French sites. Eligible patients received SNM therapy for overactive bladder (OAB) and non-obstructive urinary retention based on local standard of care. Overall, 320 patients were enrolled; 247 received permanent implant or replacement; 204 implanted patients completed second follow-up after mean of 10.0±3.8 mo.
Effectiveness outcomes were change in voids, leaks, and catheterizations/day. Other outcomes included validated QoL and disease severity scores as well as PROs and adverse event data. Outcomes at follow-ups were compared with baseline using the Wilcoxon signed-rank test.
Voids in urinary frequency (UF) and leaks/day in urinary urge incontinence (UI) patients were significantly reduced after 10 mo in both de novo (mean baseline voids/day UF de novo: 12.7 vs 8.6 after 10 mo; p<0.001; mean baseline leaks/day UI de novo: 4.3 vs 1.1 after 10 mo; p<0.001) and replacement patients (mean baseline voids/day UF replacement: 11.5 vs 7.9 after 10 mo; p<0.001; mean baseline leaks/day UI replacement: 5.4 vs 1.0 after 10 mo; p<0.001). Disease bother, Urinary Symptom Profile score, and Ditrovie questionnaire score were also significantly improved. Revisions postimplant occurred in 20% of patients including in 9% due to permanent explantation during a mean exposure time of 24.3 mo.
Through a real-life study, SOUNDS (Sacral neuromOdUlation with InterStim™ therapy for intractable lower uriNary tract DySfunctions) confirms the clinical effectiveness, safety, and positive effect of SNM on QoL and PROs for the treatment of OAB patients.
These analyses on French patients who received sacral neuromodulation (SNM) for retention or OAB during a 10-mo period showed that SNM improved OAB symptoms, quality of life, and reduced disease bother.
ClinicalTrials.gov: NCT02186041.
支持使用骶神经调节(SNM)治疗下尿路功能障碍的真实世界数据仍然受到关注。
评估 InterStim 系统在植入后 1 年内的真实生活中,SNM 在治疗下尿路功能障碍方面的有效性、生活质量(QoL)、患者报告的结果(PROs)和安全性。
设计、地点和参与者:这是一项在 25 个有代表性的公共和私人法国地点进行的前瞻性、多中心、观察性研究。根据当地的护理标准,接受 SNM 治疗的患者患有膀胱过度活动症(OAB)和非梗阻性尿潴留。共有 320 名患者入组;247 名患者接受了永久性植入或更换;204 名植入患者在平均 10.0±3.8 个月后完成了第二次随访。
有效性结果为排尿次数、漏尿和导尿次数/天的变化。其他结果包括经过验证的 QoL 和疾病严重程度评分以及 PROs 和不良事件数据。使用 Wilcoxon 符号秩检验比较随访时与基线时的结果。
在新诊断(平均基线每日排尿次数 UF 新诊断:12.7 与 10 个月后 8.6;p<0.001;平均基线每日漏尿次数 UI 新诊断:4.3 与 10 个月后 1.1;p<0.001)和更换患者(平均基线每日排尿次数 UF 更换:11.5 与 10 个月后 7.9;p<0.001;平均基线每日漏尿次数 UI 更换:5.4 与 10 个月后 1.0;p<0.001)中,OAB 和急迫性尿失禁患者的每日排尿量和漏尿量在 10 个月后显著减少。疾病困扰、尿症状评分和 Ditrovie 问卷评分也得到了显著改善。植入后发生了 20%的修订,包括 9%的患者因永久性植入而在平均 24.3 个月的暴露时间内永久植入。
通过真实世界的研究,SOUNDS(骶神经调节治疗难治性下尿路功能障碍的 InterStim 疗法)证实了 SNM 在治疗 OAB 患者方面的临床疗效、安全性以及对 QoL 和 PROs 的积极影响。
这些对法国患者的分析表明,接受骶神经调节(SNM)治疗尿潴留或 OAB 的患者,SNM 可改善 OAB 症状、生活质量并减轻疾病困扰。
ClinicalTrials.gov:NCT02186041。