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“It means you are grounded” – caregivers’ perspectives on the rehabilitation of children with neurodisability in Malawi

Purpose: Rates of childhood disability are estimated to be high in African settings; however, services to provide information and support are limited. This study aims to explore perspectives and experiences of caregivers of children with disabilities (CWD) from acquired brain injury to inform the de...

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Autores principales: Paget, Amelia, Mallewa, Macpherson, Chinguo, Dorothy, Mahebere-Chirambo, Chawanangwa, Gladstone, Melissa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4720048/
https://www.ncbi.nlm.nih.gov/pubmed/25879468
http://dx.doi.org/10.3109/09638288.2015.1035458
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author Paget, Amelia
Mallewa, Macpherson
Chinguo, Dorothy
Mahebere-Chirambo, Chawanangwa
Gladstone, Melissa
author_facet Paget, Amelia
Mallewa, Macpherson
Chinguo, Dorothy
Mahebere-Chirambo, Chawanangwa
Gladstone, Melissa
author_sort Paget, Amelia
collection PubMed
description Purpose: Rates of childhood disability are estimated to be high in African settings; however, services to provide information and support are limited. This study aims to explore perspectives and experiences of caregivers of children with disabilities (CWD) from acquired brain injury to inform the development of training packages for health-workers (HW) in hospital settings. Methods: The study was conducted in a tertiary hospital using qualitative methods. Fourteen in-depth interviews (IDIs) were conducted with parents/carers (PC), and 10 IDIs and 4 focus-group discussions (FGDs) with HW. Data were audio-recorded, transcribed, translated and analysed using thematic approaches. Results: HWs and PCs held varying perspectives on aetiology and prognosis for CWD. HWs raised concerns about impact on families, risks of neglect and abuse. Barriers to care and support included prioritisation of acute illness, lack of HW knowledge and confidence, stigma, poor communication, focus on physical disability, and poor availability of services. Among ideas for improvement, good communication and counselling was seen as a priority but not often achieved. Conclusion: A range of family, health service and wider contextual factors affect care for CWD. Training for HW should emphasise disability rights, access to services, a range of disabilities and specific training on counselling. IMPLICATIONS FOR REHABILITATION: To create good training programmes for workers who manage children with neurodisability, workers’ views on their training needs, as well parents’ views of what feel they need to know most, must be taken into account. The need for training regarding communication skills is a priority for health-workers (HW), who manage children with neurodisability in Malawi and confidence in this area is likely to be vital in providing support for these families. Disability rights and inclusion should be imperative in any training programme for managing children with neurodisability in hospital settings. Even in low-resource settings such as Malawi, it is vital that the links between hospital management and the limited resources in the community are updated and maintained.
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spelling pubmed-47200482016-02-05 “It means you are grounded” – caregivers’ perspectives on the rehabilitation of children with neurodisability in Malawi Paget, Amelia Mallewa, Macpherson Chinguo, Dorothy Mahebere-Chirambo, Chawanangwa Gladstone, Melissa Disabil Rehabil Research Paper Purpose: Rates of childhood disability are estimated to be high in African settings; however, services to provide information and support are limited. This study aims to explore perspectives and experiences of caregivers of children with disabilities (CWD) from acquired brain injury to inform the development of training packages for health-workers (HW) in hospital settings. Methods: The study was conducted in a tertiary hospital using qualitative methods. Fourteen in-depth interviews (IDIs) were conducted with parents/carers (PC), and 10 IDIs and 4 focus-group discussions (FGDs) with HW. Data were audio-recorded, transcribed, translated and analysed using thematic approaches. Results: HWs and PCs held varying perspectives on aetiology and prognosis for CWD. HWs raised concerns about impact on families, risks of neglect and abuse. Barriers to care and support included prioritisation of acute illness, lack of HW knowledge and confidence, stigma, poor communication, focus on physical disability, and poor availability of services. Among ideas for improvement, good communication and counselling was seen as a priority but not often achieved. Conclusion: A range of family, health service and wider contextual factors affect care for CWD. Training for HW should emphasise disability rights, access to services, a range of disabilities and specific training on counselling. IMPLICATIONS FOR REHABILITATION: To create good training programmes for workers who manage children with neurodisability, workers’ views on their training needs, as well parents’ views of what feel they need to know most, must be taken into account. The need for training regarding communication skills is a priority for health-workers (HW), who manage children with neurodisability in Malawi and confidence in this area is likely to be vital in providing support for these families. Disability rights and inclusion should be imperative in any training programme for managing children with neurodisability in hospital settings. Even in low-resource settings such as Malawi, it is vital that the links between hospital management and the limited resources in the community are updated and maintained. Taylor & Francis 2016-01-30 2015-04-16 /pmc/articles/PMC4720048/ /pubmed/25879468 http://dx.doi.org/10.3109/09638288.2015.1035458 Text en © 2015 The Author(s). Published by Taylor & Francis. http://creativecommons.org/licenses/by/4.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Paper
Paget, Amelia
Mallewa, Macpherson
Chinguo, Dorothy
Mahebere-Chirambo, Chawanangwa
Gladstone, Melissa
“It means you are grounded” – caregivers’ perspectives on the rehabilitation of children with neurodisability in Malawi
title “It means you are grounded” – caregivers’ perspectives on the rehabilitation of children with neurodisability in Malawi
title_full “It means you are grounded” – caregivers’ perspectives on the rehabilitation of children with neurodisability in Malawi
title_fullStr “It means you are grounded” – caregivers’ perspectives on the rehabilitation of children with neurodisability in Malawi
title_full_unstemmed “It means you are grounded” – caregivers’ perspectives on the rehabilitation of children with neurodisability in Malawi
title_short “It means you are grounded” – caregivers’ perspectives on the rehabilitation of children with neurodisability in Malawi
title_sort “it means you are grounded” – caregivers’ perspectives on the rehabilitation of children with neurodisability in malawi
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4720048/
https://www.ncbi.nlm.nih.gov/pubmed/25879468
http://dx.doi.org/10.3109/09638288.2015.1035458
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