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一项关于多发性硬化症患者胫后神经刺激的前瞻性观察性队列研究:设计与方法。

A prospective observational cohort study of posterior tibial nerve stimulation in patients with multiple sclerosis: design and methods.

机构信息

Department of Urology, University of Michigan, 1500 East Medical Drive, Taubman Center 3875, Ann Arbor, MI, 48109, USA.

Department of Neurology, University of Michigan, Ann Arbor, MI, USA.

出版信息

BMC Urol. 2020 May 27;20(1):58. doi: 10.1186/s12894-020-00629-y.

Abstract

BACKGROUND

Posterior tibial nerve stimulation (PTNS) is a promising treatment for lower urinary tract symptoms (LUTS) in patients with MS. However, long term data focusing on PTNS impact on health-related quality of life (HRQOL), bowel and bladder symptoms are lacking. This paper describes a study protocol that examines the extended efficacy of PTNS on MS related bladder and bowel symptoms and resulting HRQOL.

METHODS/DESIGN: This is a single-centered, prospective, longitudinal, observational cohort study of patients with MS who suffer from LUTS and are refractory to two prior treatment modalities. Participants who have elected to pursue PTNS therapy for LUTS will be eligible. The primary outcome is the median number of urinary frequency and incontinence episodes on a 3-day voiding diary at 3, 12 and 24 months compared to baseline. Secondary outcome measures will include change in total AUA-SS, M-ISI, NBSS, SF-12, SSS and BCS scores from baseline The Expanded Disability Status Scale and magnetic resonance imaging will be evaluated at baseline and annually throughout the study.

DISCUSSION

This research protocol aims to expand on the existing literature regarding outcomes of PTNS in MS. Specifically, it will provide long term follow-up data on bladder, bowel, sexual and HRQOL outcomes. The completion of this study will provide longitudinal efficacy data of the impact of PTNS in MS patients.

TRIAL REGISTRATION

NCT04063852.

摘要

背景

胫骨后神经刺激(PTNS)是治疗多发性硬化症(MS)患者下尿路症状(LUTS)的一种很有前途的方法。然而,缺乏专注于 PTNS 对健康相关生活质量(HRQOL)、肠和膀胱症状影响的长期数据。本文描述了一项研究方案,该方案检查了 PTNS 对 MS 相关膀胱和肠道症状以及由此产生的 HRQOL 的扩展疗效。

方法/设计:这是一项单中心、前瞻性、纵向、观察性队列研究,纳入患有 LUTS 且对两种先前治疗方法均无反应的 MS 患者。选择 PTNS 治疗 LUTS 的患者将符合入选条件。主要结局是与基线相比,3 天排尿日记中尿频数和失禁发作的中位数在 3、12 和 24 个月时的变化。次要结局指标将包括从基线开始时的 AUA-SS、M-ISI、NBSS、SF-12、SSS 和 BCS 评分的变化。扩展残疾状况量表和磁共振成像将在基线和研究期间每年进行评估。

讨论

本研究方案旨在扩展关于 PTNS 在 MS 中疗效的现有文献。具体而言,它将提供关于膀胱、肠道、性功能和 HRQOL 结局的长期随访数据。该研究的完成将提供 PTNS 在 MS 患者中的长期疗效数据。

试验注册

NCT04063852。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/80f7/7251681/8074223d2fd8/12894_2020_629_Fig1_HTML.jpg

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