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Needs of informal caregivers across the caregiving course in amyotrophic lateral sclerosis: a qualitative analysis
OBJECTIVES: Amyotrophic lateral sclerosis (ALS), also known as motor neuron disease (MND), is a debilitating terminal condition. Informal caregivers are key figures in ALS care provision. The physical, psychological and emotional impact of providing care in the home requires appropriate assistance a...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BMJ Publishing Group
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5829772/ https://www.ncbi.nlm.nih.gov/pubmed/29374665 http://dx.doi.org/10.1136/bmjopen-2017-018721 |
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author | Galvin, Miriam Carney, Sile Corr, Bernie Mays, Iain Pender, Niall Hardiman, Orla |
author_facet | Galvin, Miriam Carney, Sile Corr, Bernie Mays, Iain Pender, Niall Hardiman, Orla |
author_sort | Galvin, Miriam |
collection | PubMed |
description | OBJECTIVES: Amyotrophic lateral sclerosis (ALS), also known as motor neuron disease (MND), is a debilitating terminal condition. Informal caregivers are key figures in ALS care provision. The physical, psychological and emotional impact of providing care in the home requires appropriate assistance and support. The objective of this analysis is to explore the needs of informal ALS caregivers across the caregiving course. DESIGN: In an open-ended question as part of a semistructured interview, caregivers were asked what would help them in their role. Interviews took place on three occasions at 4-month to 6-month intervals. Demographic, burden and quality of life data were collected, in addition to the open-ended responses. We carried out descriptive statistical analysis and thematic analysis of qualitative data. SETTING AND PARTICIPANTS: Home interviews at baseline (n=81) and on two further occasions (n=56, n=41) with informal caregivers of people with ALS attending the National ALS/MND Clinic at Beaumont Hospital, Dublin, Ireland. RESULTS: The majority of caregivers were family members. Hours of care provided and caregiver burden increased across the interview series. Thematic analysis identified what would help them in their role, and needs related to external support and services, psychological-emotional factors, patient-related behaviours, a cure and ‘nothing’. Themes were interconnected and their prevalence varied across the interview time points. CONCLUSION: This study has shown the consistency and adaptation in what caregivers identified as helpful in their role, across 12–18 months of a caregiving journey. Support needs are clearly defined, and change with time and the course of caregiving. Caregivers need support from family, friends and healthcare professionals in managing their tasks and the emotional demands of caregiving. Identifying the specific needs of informal caregivers should enable health professionals to provide tailored supportive interventions. |
format | Online Article Text |
id | pubmed-5829772 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BMJ Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-58297722018-03-05 Needs of informal caregivers across the caregiving course in amyotrophic lateral sclerosis: a qualitative analysis Galvin, Miriam Carney, Sile Corr, Bernie Mays, Iain Pender, Niall Hardiman, Orla BMJ Open Health Services Research OBJECTIVES: Amyotrophic lateral sclerosis (ALS), also known as motor neuron disease (MND), is a debilitating terminal condition. Informal caregivers are key figures in ALS care provision. The physical, psychological and emotional impact of providing care in the home requires appropriate assistance and support. The objective of this analysis is to explore the needs of informal ALS caregivers across the caregiving course. DESIGN: In an open-ended question as part of a semistructured interview, caregivers were asked what would help them in their role. Interviews took place on three occasions at 4-month to 6-month intervals. Demographic, burden and quality of life data were collected, in addition to the open-ended responses. We carried out descriptive statistical analysis and thematic analysis of qualitative data. SETTING AND PARTICIPANTS: Home interviews at baseline (n=81) and on two further occasions (n=56, n=41) with informal caregivers of people with ALS attending the National ALS/MND Clinic at Beaumont Hospital, Dublin, Ireland. RESULTS: The majority of caregivers were family members. Hours of care provided and caregiver burden increased across the interview series. Thematic analysis identified what would help them in their role, and needs related to external support and services, psychological-emotional factors, patient-related behaviours, a cure and ‘nothing’. Themes were interconnected and their prevalence varied across the interview time points. CONCLUSION: This study has shown the consistency and adaptation in what caregivers identified as helpful in their role, across 12–18 months of a caregiving journey. Support needs are clearly defined, and change with time and the course of caregiving. Caregivers need support from family, friends and healthcare professionals in managing their tasks and the emotional demands of caregiving. Identifying the specific needs of informal caregivers should enable health professionals to provide tailored supportive interventions. BMJ Publishing Group 2018-01-27 /pmc/articles/PMC5829772/ /pubmed/29374665 http://dx.doi.org/10.1136/bmjopen-2017-018721 Text en © Article author(s) (or their employer(s) unless otherwise stated in the text of the article) 2018. All rights reserved. No commercial use is permitted unless otherwise expressly granted. This is an Open Access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/ |
spellingShingle | Health Services Research Galvin, Miriam Carney, Sile Corr, Bernie Mays, Iain Pender, Niall Hardiman, Orla Needs of informal caregivers across the caregiving course in amyotrophic lateral sclerosis: a qualitative analysis |
title | Needs of informal caregivers across the caregiving course in amyotrophic lateral sclerosis: a qualitative analysis |
title_full | Needs of informal caregivers across the caregiving course in amyotrophic lateral sclerosis: a qualitative analysis |
title_fullStr | Needs of informal caregivers across the caregiving course in amyotrophic lateral sclerosis: a qualitative analysis |
title_full_unstemmed | Needs of informal caregivers across the caregiving course in amyotrophic lateral sclerosis: a qualitative analysis |
title_short | Needs of informal caregivers across the caregiving course in amyotrophic lateral sclerosis: a qualitative analysis |
title_sort | needs of informal caregivers across the caregiving course in amyotrophic lateral sclerosis: a qualitative analysis |
topic | Health Services Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5829772/ https://www.ncbi.nlm.nih.gov/pubmed/29374665 http://dx.doi.org/10.1136/bmjopen-2017-018721 |
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