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Intermittent colonic exoperistalsis for chronic constipation in spinal cord-injured individuals. A long-term structured patient feedback survey to evaluate home care use

STUDY DESIGN: Structured patient feedback survey evaluating real-world home care use. OBJECTIVES: To assess the long-term effectiveness, tolerability, and satisfaction with the intermittent colonic exoperistalsis (ICE) treatment device MOWOOT in spinal cord-injured (SCI) individuals with chronic con...

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Autores principales: Bremer, Jana, Bremer, Jörn, König, Maike, Koßmehl, Peter, Kurze, Ines, Obereisenbuchner, Jeannette, Weinschenk, Elisabeth, Herrero-Fresneda, Immaculada
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10387045/
https://www.ncbi.nlm.nih.gov/pubmed/37516745
http://dx.doi.org/10.1038/s41394-023-00597-z
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author Bremer, Jana
Bremer, Jörn
König, Maike
Koßmehl, Peter
Kurze, Ines
Obereisenbuchner, Jeannette
Weinschenk, Elisabeth
Herrero-Fresneda, Immaculada
author_facet Bremer, Jana
Bremer, Jörn
König, Maike
Koßmehl, Peter
Kurze, Ines
Obereisenbuchner, Jeannette
Weinschenk, Elisabeth
Herrero-Fresneda, Immaculada
author_sort Bremer, Jana
collection PubMed
description STUDY DESIGN: Structured patient feedback survey evaluating real-world home care use. OBJECTIVES: To assess the long-term effectiveness, tolerability, and satisfaction with the intermittent colonic exoperistalsis (ICE) treatment device MOWOOT in spinal cord-injured (SCI) individuals with chronic constipation. SETTING: Four specialized German hospitals. METHODS: SCI individuals with chronic constipation were invited to use MOWOOT 10–20 min daily and answer a questionnaire about their bowel situation before treatment (feedback 1, F1) and after ≥10 months of use (feedback 2, F2). Collected variables were device use, bowel function effectiveness, chronic constipation symptoms, concomitant use of laxatives and evacuation aids, and satisfaction with bowel function and management, which were compared between time points. At F2, participants reported efficacy, tolerability/side effects, and ease of use. RESULTS: Eleven participants used the device for a mean (SD) of 13.27 (4.03) months. From F1 to F2, mean time per evacuation decreased by 24.5 min (p = 0.0076) and the number of failed attempts to evacuate/week, by 1.05 (p = 0.0354) with a tendency toward increased bowel movements and softer stool consistency, and decreased incomplete bowel movements. Participants experienced decreased difficulty/strain (p = 0.0055), abdominal pain (p = 0.0230), bloating (p = 0.0010), abdominal cramps (p = 0.0019), and spasms (p = 0.0198), without significant changes in the use of laxatives and evacuation aids. Satisfaction with bowel function and management improved (p = 0.0095) and more participants reported being very satisfied/satisfied (p = 0.0300). Most reported tolerability, efficacy, and ease of use as very good/good. CONCLUSION: Long-term in-home ICE treatment improved bowel function and chronic constipation symptoms in SCI individuals, providing clinical benefits to this population. SPONSORSHIP (MOWOOT DEVICES LENDING): 4 M Medical GmbH, Norderstedt, Germany.
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spelling pubmed-103870452023-07-31 Intermittent colonic exoperistalsis for chronic constipation in spinal cord-injured individuals. A long-term structured patient feedback survey to evaluate home care use Bremer, Jana Bremer, Jörn König, Maike Koßmehl, Peter Kurze, Ines Obereisenbuchner, Jeannette Weinschenk, Elisabeth Herrero-Fresneda, Immaculada Spinal Cord Ser Cases Article STUDY DESIGN: Structured patient feedback survey evaluating real-world home care use. OBJECTIVES: To assess the long-term effectiveness, tolerability, and satisfaction with the intermittent colonic exoperistalsis (ICE) treatment device MOWOOT in spinal cord-injured (SCI) individuals with chronic constipation. SETTING: Four specialized German hospitals. METHODS: SCI individuals with chronic constipation were invited to use MOWOOT 10–20 min daily and answer a questionnaire about their bowel situation before treatment (feedback 1, F1) and after ≥10 months of use (feedback 2, F2). Collected variables were device use, bowel function effectiveness, chronic constipation symptoms, concomitant use of laxatives and evacuation aids, and satisfaction with bowel function and management, which were compared between time points. At F2, participants reported efficacy, tolerability/side effects, and ease of use. RESULTS: Eleven participants used the device for a mean (SD) of 13.27 (4.03) months. From F1 to F2, mean time per evacuation decreased by 24.5 min (p = 0.0076) and the number of failed attempts to evacuate/week, by 1.05 (p = 0.0354) with a tendency toward increased bowel movements and softer stool consistency, and decreased incomplete bowel movements. Participants experienced decreased difficulty/strain (p = 0.0055), abdominal pain (p = 0.0230), bloating (p = 0.0010), abdominal cramps (p = 0.0019), and spasms (p = 0.0198), without significant changes in the use of laxatives and evacuation aids. Satisfaction with bowel function and management improved (p = 0.0095) and more participants reported being very satisfied/satisfied (p = 0.0300). Most reported tolerability, efficacy, and ease of use as very good/good. CONCLUSION: Long-term in-home ICE treatment improved bowel function and chronic constipation symptoms in SCI individuals, providing clinical benefits to this population. SPONSORSHIP (MOWOOT DEVICES LENDING): 4 M Medical GmbH, Norderstedt, Germany. Nature Publishing Group UK 2023-07-29 /pmc/articles/PMC10387045/ /pubmed/37516745 http://dx.doi.org/10.1038/s41394-023-00597-z Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Bremer, Jana
Bremer, Jörn
König, Maike
Koßmehl, Peter
Kurze, Ines
Obereisenbuchner, Jeannette
Weinschenk, Elisabeth
Herrero-Fresneda, Immaculada
Intermittent colonic exoperistalsis for chronic constipation in spinal cord-injured individuals. A long-term structured patient feedback survey to evaluate home care use
title Intermittent colonic exoperistalsis for chronic constipation in spinal cord-injured individuals. A long-term structured patient feedback survey to evaluate home care use
title_full Intermittent colonic exoperistalsis for chronic constipation in spinal cord-injured individuals. A long-term structured patient feedback survey to evaluate home care use
title_fullStr Intermittent colonic exoperistalsis for chronic constipation in spinal cord-injured individuals. A long-term structured patient feedback survey to evaluate home care use
title_full_unstemmed Intermittent colonic exoperistalsis for chronic constipation in spinal cord-injured individuals. A long-term structured patient feedback survey to evaluate home care use
title_short Intermittent colonic exoperistalsis for chronic constipation in spinal cord-injured individuals. A long-term structured patient feedback survey to evaluate home care use
title_sort intermittent colonic exoperistalsis for chronic constipation in spinal cord-injured individuals. a long-term structured patient feedback survey to evaluate home care use
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10387045/
https://www.ncbi.nlm.nih.gov/pubmed/37516745
http://dx.doi.org/10.1038/s41394-023-00597-z
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