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A meta-ethnography to understand the experience of living with urinary incontinence: ‘is it just part and parcel of life?’

BACKGROUND: Urinary incontinence (UI) is highly prevalent and affects the lives of many men and women. We aimed to conduct a qualitative evidence synthesis (QES) to explore the experience of living with UI and to develop a conceptual model that can help us to understand this experience, and the pote...

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Autores principales: Toye, Francine, Barker, Karen L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6964106/
https://www.ncbi.nlm.nih.gov/pubmed/31941470
http://dx.doi.org/10.1186/s12894-019-0555-4
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author Toye, Francine
Barker, Karen L.
author_facet Toye, Francine
Barker, Karen L.
author_sort Toye, Francine
collection PubMed
description BACKGROUND: Urinary incontinence (UI) is highly prevalent and affects the lives of many men and women. We aimed to conduct a qualitative evidence synthesis (QES) to explore the experience of living with UI and to develop a conceptual model that can help us to understand this experience, and the potential barriers to appropriate healthcare. METHODS: We used the methods of meta-ethnography developed by Noblit and Hare and recently refined for larger studies. Meta-ethnography involves identifying concepts from the studies and abstracting these concepts into a line of argument. We searched for studies that explored the experience of adults with UI. We used the GRADE-CERQual framework to assess confidence in review findings. RESULTS: We screened 2307 titles, 429 abstracts, 107 full texts and included 41 studies (36 unique samples) in the synthesis. We organised the concepts into 26 conceptual categories, which we further abstracted into 6 themes: (1) Am I ill or is this normal? (2) It effects who I am and how I feel; (3) I feel stigmatised, ashamed and guilty; (4) talking can be difficult but it can help; (5) keeping incontinence under control; (6) have I got to the point that I need help? Our model conceptualises living with UI as navigating antagonists: Is UI normal or am I ill? Do I need help or am I managing? Do I keep UI to myself (and manage alone) or do I tell other people (and get the support that I need)? Do I use control strategies that focus on concealing (avoid risky situations, wear pads) versus, I use strategies that focus on improving the bodily function to improve continence. Our model highlights the experience of stigma, shame and guilt which exert a pull towards concealment. CONCLUSIONS: The culture of secrecy and profound sense of shame is barrier to seeking help. An environment which reduces the shame and stigma of UI may help people to switch the focus to strategies that will improve continence, rather than conceal incontinence.
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spelling pubmed-69641062020-01-22 A meta-ethnography to understand the experience of living with urinary incontinence: ‘is it just part and parcel of life?’ Toye, Francine Barker, Karen L. BMC Urol Research Article BACKGROUND: Urinary incontinence (UI) is highly prevalent and affects the lives of many men and women. We aimed to conduct a qualitative evidence synthesis (QES) to explore the experience of living with UI and to develop a conceptual model that can help us to understand this experience, and the potential barriers to appropriate healthcare. METHODS: We used the methods of meta-ethnography developed by Noblit and Hare and recently refined for larger studies. Meta-ethnography involves identifying concepts from the studies and abstracting these concepts into a line of argument. We searched for studies that explored the experience of adults with UI. We used the GRADE-CERQual framework to assess confidence in review findings. RESULTS: We screened 2307 titles, 429 abstracts, 107 full texts and included 41 studies (36 unique samples) in the synthesis. We organised the concepts into 26 conceptual categories, which we further abstracted into 6 themes: (1) Am I ill or is this normal? (2) It effects who I am and how I feel; (3) I feel stigmatised, ashamed and guilty; (4) talking can be difficult but it can help; (5) keeping incontinence under control; (6) have I got to the point that I need help? Our model conceptualises living with UI as navigating antagonists: Is UI normal or am I ill? Do I need help or am I managing? Do I keep UI to myself (and manage alone) or do I tell other people (and get the support that I need)? Do I use control strategies that focus on concealing (avoid risky situations, wear pads) versus, I use strategies that focus on improving the bodily function to improve continence. Our model highlights the experience of stigma, shame and guilt which exert a pull towards concealment. CONCLUSIONS: The culture of secrecy and profound sense of shame is barrier to seeking help. An environment which reduces the shame and stigma of UI may help people to switch the focus to strategies that will improve continence, rather than conceal incontinence. BioMed Central 2020-01-16 /pmc/articles/PMC6964106/ /pubmed/31941470 http://dx.doi.org/10.1186/s12894-019-0555-4 Text en © The Author(s). 2020 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Toye, Francine
Barker, Karen L.
A meta-ethnography to understand the experience of living with urinary incontinence: ‘is it just part and parcel of life?’
title A meta-ethnography to understand the experience of living with urinary incontinence: ‘is it just part and parcel of life?’
title_full A meta-ethnography to understand the experience of living with urinary incontinence: ‘is it just part and parcel of life?’
title_fullStr A meta-ethnography to understand the experience of living with urinary incontinence: ‘is it just part and parcel of life?’
title_full_unstemmed A meta-ethnography to understand the experience of living with urinary incontinence: ‘is it just part and parcel of life?’
title_short A meta-ethnography to understand the experience of living with urinary incontinence: ‘is it just part and parcel of life?’
title_sort meta-ethnography to understand the experience of living with urinary incontinence: ‘is it just part and parcel of life?’
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6964106/
https://www.ncbi.nlm.nih.gov/pubmed/31941470
http://dx.doi.org/10.1186/s12894-019-0555-4
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