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A retrospective study of neuromuscular electrical stimulation for treating women with post-stroke incontinence

This retrospective study evaluated the effect of using neuromuscular electrical stimulation (NMES) for the treatment of post-stroke urinary incontinence (PSUI) among female population in China. A total of 163 eligible patients with PSUI were included in this study. Of these, 103 patients were assign...

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Autores principales: Shen, Shu-Xia, Liu, Yun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6039598/
https://www.ncbi.nlm.nih.gov/pubmed/29952999
http://dx.doi.org/10.1097/MD.0000000000011264
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author Shen, Shu-Xia
Liu, Yun
author_facet Shen, Shu-Xia
Liu, Yun
author_sort Shen, Shu-Xia
collection PubMed
description This retrospective study evaluated the effect of using neuromuscular electrical stimulation (NMES) for the treatment of post-stroke urinary incontinence (PSUI) among female population in China. A total of 163 eligible patients with PSUI were included in this study. Of these, 103 patients were assigned to a treatment group, and 60 subjects were assigned to a control group. All patients in both groups received bladder training. In addition, patients in the treatment group also received NMES. All patients were treated for a total of 8 weeks. The outcome measurements included the amount of urine leakage, urinary symptoms and quality of life. The urinary symptoms were measured by the Bristol Female Urinary Symptoms Questionnaire (BFUSQ) score, and the quality of life was assessed by the International Consultation on Incontinence Questionnaire-Short Form (ICIQ-SF) score. In addition, adverse events were also documented in this study. After 4-week treatment, patients who received NMES did not exert better outcomes in the amount of urine leakage, urinary symptoms, measured by BFUSQ scale, and the quality of life, assessed by ICIQ-SF scale. However, after 8-week treatment, patients in the treatment group showed greater effect in reducing the amount of urine leakage (P < .01), enhancing urinary symptoms, as measured by BFUSQ scale (P < .01), and improving the quality of life, as assessed by ICIQ-SF scale (P < .01), compared with patients in the control group. In addition, no adverse event was recorded during the period of 8-week treatment in this study. The results of this study indicated that NMES may benefit for patients with PSUI after 8-week treatment. Future studies should focus on warranting the results of this study.
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spelling pubmed-60395982018-07-16 A retrospective study of neuromuscular electrical stimulation for treating women with post-stroke incontinence Shen, Shu-Xia Liu, Yun Medicine (Baltimore) Research Article This retrospective study evaluated the effect of using neuromuscular electrical stimulation (NMES) for the treatment of post-stroke urinary incontinence (PSUI) among female population in China. A total of 163 eligible patients with PSUI were included in this study. Of these, 103 patients were assigned to a treatment group, and 60 subjects were assigned to a control group. All patients in both groups received bladder training. In addition, patients in the treatment group also received NMES. All patients were treated for a total of 8 weeks. The outcome measurements included the amount of urine leakage, urinary symptoms and quality of life. The urinary symptoms were measured by the Bristol Female Urinary Symptoms Questionnaire (BFUSQ) score, and the quality of life was assessed by the International Consultation on Incontinence Questionnaire-Short Form (ICIQ-SF) score. In addition, adverse events were also documented in this study. After 4-week treatment, patients who received NMES did not exert better outcomes in the amount of urine leakage, urinary symptoms, measured by BFUSQ scale, and the quality of life, assessed by ICIQ-SF scale. However, after 8-week treatment, patients in the treatment group showed greater effect in reducing the amount of urine leakage (P < .01), enhancing urinary symptoms, as measured by BFUSQ scale (P < .01), and improving the quality of life, as assessed by ICIQ-SF scale (P < .01), compared with patients in the control group. In addition, no adverse event was recorded during the period of 8-week treatment in this study. The results of this study indicated that NMES may benefit for patients with PSUI after 8-week treatment. Future studies should focus on warranting the results of this study. Wolters Kluwer Health 2018-06-29 /pmc/articles/PMC6039598/ /pubmed/29952999 http://dx.doi.org/10.1097/MD.0000000000011264 Text en Copyright © 2018 the Author(s). Published by Wolters Kluwer Health, Inc. http://creativecommons.org/licenses/by-nc/4.0 This is an open access article distributed under the terms of the Creative Commons Attribution-Non Commercial License 4.0 (CCBY-NC), where it is permissible to download, share, remix, transform, and buildup the work provided it is properly cited. The work cannot be used commercially without permission from the journal. http://creativecommons.org/licenses/by-nc/4.0
spellingShingle Research Article
Shen, Shu-Xia
Liu, Yun
A retrospective study of neuromuscular electrical stimulation for treating women with post-stroke incontinence
title A retrospective study of neuromuscular electrical stimulation for treating women with post-stroke incontinence
title_full A retrospective study of neuromuscular electrical stimulation for treating women with post-stroke incontinence
title_fullStr A retrospective study of neuromuscular electrical stimulation for treating women with post-stroke incontinence
title_full_unstemmed A retrospective study of neuromuscular electrical stimulation for treating women with post-stroke incontinence
title_short A retrospective study of neuromuscular electrical stimulation for treating women with post-stroke incontinence
title_sort retrospective study of neuromuscular electrical stimulation for treating women with post-stroke incontinence
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6039598/
https://www.ncbi.nlm.nih.gov/pubmed/29952999
http://dx.doi.org/10.1097/MD.0000000000011264
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