Literature DB >> 25801920

Bladder dysfunction and quality of life for people with multiple sclerosis.

Catherine Browne1, Nancy Salmon1, Maria Kehoe2.   

Abstract

PURPOSE: Bladder dysfunction affects 75% of people with multiple sclerosis (MS). People with MS are reluctant to seek treatment for this distressing symptom. This is the first-known study to explore in depth how bladder dysfunction interferes with quality of life for people with MS.
METHODS: Nineteen individual semi-structured interviews were conducted (M = 8, F = 11). Participants had a definite diagnosis of MS, aged between 37 and 64 years and had at least one bladder dysfunction symptom. The audio-recorded interviews lasted up to 90 min and were transcribed verbatim.
RESULTS: Thematic analysis within NVivo10 yielded two key themes: (1) Disruptions and loss and (2) ways of knowing. "Disruptions and Loss" explores how bladder dysfunction interrupted daily living activities and how this contributed to experiencing loss. "Ways of knowing" portrays the types of knowledge that existed around bladder dysfunction. Participants described using their experiential knowledge to self-manage bladder symptoms without advice from healthcare providers.
CONCLUSIONS: Bladder dysfunction imposes major disruptions on daily life. People with MS attempt to self-manage their bladder symptoms, despite current barriers to navigating existing healthcare infrastructure. Understanding these barriers and the individual strategies employed by people with MS are the first steps in facilitating independent management of bladder dysfunction. Implications for Rehabilitation Each individual's experience of bladder dysfunction is unique. Healthcare professionals must be prepared to discuss all disruptions and losses associated with bladder dysfunction for people with MS. People with MS have a vast range of knowledge in relation to their own bladder symptoms and healthcare professionals need to explore their existing self-management strategies during assessment. People with MS and healthcare professionals need to be educated on the wider health implications relating to bladder dysfunction.

Entities:  

Keywords:  Neurogenic bladder; participation; urinary incontinence

Mesh:

Year:  2015        PMID: 25801920     DOI: 10.3109/09638288.2015.1027007

Source DB:  PubMed          Journal:  Disabil Rehabil        ISSN: 0963-8288            Impact factor:   3.033


  9 in total

1.  How Beliefs About Bladder Dysfunction Among Health-Care Professionals Influence Clinical Practice Development: Perspectives of Allied Health Professionals, Nurses, and Managers.

Authors:  Catherine Browne; Maria Kehoe; Nancy Salmon
Journal:  Int J MS Care       Date:  2017 Jul-Aug

Review 2.  Autonomic Dysregulation in Multiple Sclerosis.

Authors:  Alexandra Pintér; Domonkos Cseh; Adrienn Sárközi; Ben M Illigens; Timo Siepmann
Journal:  Int J Mol Sci       Date:  2015-07-24       Impact factor: 5.923

Review 3.  'It struck at the heart of who I thought I was': A meta-synthesis of the qualitative literature examining the experiences of people with multiple sclerosis.

Authors:  Jane Desborough; Crystal Brunoro; Anne Parkinson; Katrina Chisholm; Mark Elisha; Janet Drew; Vanessa Fanning; Christian Lueck; Anne Bruestle; Matthew Cook; Hanna Suominen; Antonio Tricoli; Adam Henschke; Christine Phillips
Journal:  Health Expect       Date:  2020-06-24       Impact factor: 3.377

Review 4.  Comprehensive Approach to Management of Multiple Sclerosis: Addressing Invisible Symptoms-A Narrative Review.

Authors:  Lynsey Lakin; Bryan E Davis; Cherie C Binns; Keisha M Currie; Mary R Rensel
Journal:  Neurol Ther       Date:  2021-04-20

5.  Feasibility and acceptability of transcutaneous tibial nerve stimulation for the treatment of bladder storage symptoms among people with multiple sclerosis.

Authors:  Hawra B Al Dandan; Rose Galvin; Katie Robinson; Doreen McClurg; Susan Coote
Journal:  Pilot Feasibility Stud       Date:  2022-07-30

6.  Prevalence of Lower Urinary Tract Symptoms in People with Multiple Sclerosis: A Systematic Review and Meta-analysis.

Authors:  Hawra B Al Dandan; Susan Coote; Doreen McClurg
Journal:  Int J MS Care       Date:  2020 Mar-Apr

Review 7.  Patient Work and Their Contexts: Scoping Review.

Authors:  Kathleen Yin; Joshua Jung; Enrico Coiera; Liliana Laranjo; Ann Blandford; Adeel Khoja; Wan-Tien Tai; Daniel Psillakis Phillips; Annie Y S Lau
Journal:  J Med Internet Res       Date:  2020-06-02       Impact factor: 5.428

8.  Management strategies for lower urinary tract symptoms (LUTS) among people with multiple sclerosis (MS): a qualitative study of the perspectives of people with MS and healthcare professionals.

Authors:  Hawra B Al Dandan; Rose Galvin; Doreen McClurg; Susan Coote
Journal:  HRB Open Res       Date:  2019-11-18

9.  Assessment of factors associated with depression and anxiety among pwMS in Saudi Arabia.

Authors:  Safanah AlSaeed; Nuha M Alkhawajah; Mohsen Ayyash; Salman Aljarallah; Rola Alarieh; Amani Abu-Shaheen
Journal:  BMC Neurol       Date:  2022-03-25       Impact factor: 2.474

  9 in total

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