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Patient Priorities in Autoimmune Hepatitis: The Need for Better Treatments, More Education and Challenging Stigma
BACKGROUND: Data show that patients with autoimmune hepatitis have significantly reduced quality-of-life and that corticosteroids carry marked side effects. AIMS: This study explored patients’ experiences of autoimmune hepatitis and its treatments; key aspects for developing safe and effective new a...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer US
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9112273/ https://www.ncbi.nlm.nih.gov/pubmed/35579795 http://dx.doi.org/10.1007/s10620-022-07525-5 |
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author | Lloyd, Charlotte Leighton, Jessica Wong, Lin Lee Goulding, Anna Brownlee, Ann Gray, Penney Culver, Emma Halliday, Neil Thorburn, Doug Heneghan, Michael A. Jones, David E. J. Exley, Catherine Dyson, Jessica K. |
author_facet | Lloyd, Charlotte Leighton, Jessica Wong, Lin Lee Goulding, Anna Brownlee, Ann Gray, Penney Culver, Emma Halliday, Neil Thorburn, Doug Heneghan, Michael A. Jones, David E. J. Exley, Catherine Dyson, Jessica K. |
author_sort | Lloyd, Charlotte |
collection | PubMed |
description | BACKGROUND: Data show that patients with autoimmune hepatitis have significantly reduced quality-of-life and that corticosteroids carry marked side effects. AIMS: This study explored patients’ experiences of autoimmune hepatitis and its treatments; key aspects for developing safe and effective new approaches to therapy. METHODS: An anonymised, internet-based survey collected data including patient demographics, treatments, side-effects, impact on day-to-day life, sources of support and attitudes towards autoimmune hepatitis between December 2019–January 2020. Semi-structured interviews were conducted with 13 patients to further explore their support networks, treatment experiences and health priorities. Descriptive and quantitative analyses were undertaken using R and free text responses were subject to thematic analysis. RESULTS: In total, 270 survey responses were received (median age 55 years and 94% female). Perceived medication side-effects were reported by 66% (169/257) and 73% responded negatively about their experience of corticosteroids. The majority (62·3% [(109/175]) would ‘definitely’ or ‘probably’ consider clinical trial participation to improve their care. Only 18·7% (31/166) reported access to a specialist liver nurse and nearly half were involved in support groups. Interview and survey data suggested that major issues were stigma, loss of control and fatigue. CONCLUSIONS: This study provides insights into the realities of living with autoimmune hepatitis with clear issues around lack of support networks, need for patient empowerment and stigma surrounding liver disease. Patient priorities are better therapies to slow disease progression, avoiding corticosteroids and minimising side-effects. Patient willingness to participate in trials suggests that they are achievable provided they have the right design and clinical endpoints. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s10620-022-07525-5. |
format | Online Article Text |
id | pubmed-9112273 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Springer US |
record_format | MEDLINE/PubMed |
spelling | pubmed-91122732022-05-17 Patient Priorities in Autoimmune Hepatitis: The Need for Better Treatments, More Education and Challenging Stigma Lloyd, Charlotte Leighton, Jessica Wong, Lin Lee Goulding, Anna Brownlee, Ann Gray, Penney Culver, Emma Halliday, Neil Thorburn, Doug Heneghan, Michael A. Jones, David E. J. Exley, Catherine Dyson, Jessica K. Dig Dis Sci Original Article BACKGROUND: Data show that patients with autoimmune hepatitis have significantly reduced quality-of-life and that corticosteroids carry marked side effects. AIMS: This study explored patients’ experiences of autoimmune hepatitis and its treatments; key aspects for developing safe and effective new approaches to therapy. METHODS: An anonymised, internet-based survey collected data including patient demographics, treatments, side-effects, impact on day-to-day life, sources of support and attitudes towards autoimmune hepatitis between December 2019–January 2020. Semi-structured interviews were conducted with 13 patients to further explore their support networks, treatment experiences and health priorities. Descriptive and quantitative analyses were undertaken using R and free text responses were subject to thematic analysis. RESULTS: In total, 270 survey responses were received (median age 55 years and 94% female). Perceived medication side-effects were reported by 66% (169/257) and 73% responded negatively about their experience of corticosteroids. The majority (62·3% [(109/175]) would ‘definitely’ or ‘probably’ consider clinical trial participation to improve their care. Only 18·7% (31/166) reported access to a specialist liver nurse and nearly half were involved in support groups. Interview and survey data suggested that major issues were stigma, loss of control and fatigue. CONCLUSIONS: This study provides insights into the realities of living with autoimmune hepatitis with clear issues around lack of support networks, need for patient empowerment and stigma surrounding liver disease. Patient priorities are better therapies to slow disease progression, avoiding corticosteroids and minimising side-effects. Patient willingness to participate in trials suggests that they are achievable provided they have the right design and clinical endpoints. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s10620-022-07525-5. Springer US 2022-05-17 2023 /pmc/articles/PMC9112273/ /pubmed/35579795 http://dx.doi.org/10.1007/s10620-022-07525-5 Text en © The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature 2022 This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic. |
spellingShingle | Original Article Lloyd, Charlotte Leighton, Jessica Wong, Lin Lee Goulding, Anna Brownlee, Ann Gray, Penney Culver, Emma Halliday, Neil Thorburn, Doug Heneghan, Michael A. Jones, David E. J. Exley, Catherine Dyson, Jessica K. Patient Priorities in Autoimmune Hepatitis: The Need for Better Treatments, More Education and Challenging Stigma |
title | Patient Priorities in Autoimmune Hepatitis: The Need for Better Treatments, More Education and Challenging Stigma |
title_full | Patient Priorities in Autoimmune Hepatitis: The Need for Better Treatments, More Education and Challenging Stigma |
title_fullStr | Patient Priorities in Autoimmune Hepatitis: The Need for Better Treatments, More Education and Challenging Stigma |
title_full_unstemmed | Patient Priorities in Autoimmune Hepatitis: The Need for Better Treatments, More Education and Challenging Stigma |
title_short | Patient Priorities in Autoimmune Hepatitis: The Need for Better Treatments, More Education and Challenging Stigma |
title_sort | patient priorities in autoimmune hepatitis: the need for better treatments, more education and challenging stigma |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9112273/ https://www.ncbi.nlm.nih.gov/pubmed/35579795 http://dx.doi.org/10.1007/s10620-022-07525-5 |
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