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Psychosocial recommendations for the care of children and adults with epidermolysis bullosa and their family: evidence based guidelines
Epidermolysis Bullosa (EB) is a group of rare genetic disorders resulting in skin fragility and other symptoms. Commissioned by DEBRA International and funded by DEBRA Norway, this evidence-bases guideline provides recommendations to optimise psychosocial wellbeing in EB. An international multidisci...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6560722/ https://www.ncbi.nlm.nih.gov/pubmed/31186066 http://dx.doi.org/10.1186/s13023-019-1086-5 |
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author | Martin, K. Geuens, S. Asche, J. K. Bodan, R. Browne, F. Downe, A. García García, N. Jaega, G. Kennedy, B. Mauritz, P. J. Pérez, F. Soon, K. Zmazek, V. Mayre-Chilton, K. M. |
author_facet | Martin, K. Geuens, S. Asche, J. K. Bodan, R. Browne, F. Downe, A. García García, N. Jaega, G. Kennedy, B. Mauritz, P. J. Pérez, F. Soon, K. Zmazek, V. Mayre-Chilton, K. M. |
author_sort | Martin, K. |
collection | PubMed |
description | Epidermolysis Bullosa (EB) is a group of rare genetic disorders resulting in skin fragility and other symptoms. Commissioned by DEBRA International and funded by DEBRA Norway, this evidence-bases guideline provides recommendations to optimise psychosocial wellbeing in EB. An international multidisciplinary panel of social and health care professionals (HCP) and people living with EB was formed. A systematic international literature review was conducted by the panel following the Scottish Intercollegiate Guidelines Network (SIGN) methodology. The resulting papers underwent systematic selection and critique processes. Included papers were allocated to 6 different outcome groups to allow data synthesis and exploration: quality of life, coping, family, wellbeing, access to HCP and pain. Based on the evidence in those papers, recommendations were made for individuals living with EB, family and caregivers and HCP working in the field. Few studies have investigated interventions and which factors lead to better outcomes, but general recommendations can be made. EB is a complex disease impacting enormously on every aspect of psychosocial life. People and families living with EB need access to multidisciplinary support, including psychological guidance, in order to improve quality of life and psychosocial wellbeing. Interventions should stimulate social participation to prevent isolation. People with EB and their families should be able to access a supportive network. HCP should be well supported and educated about the complexity of EB. They should work collaboratively with those around the individual with EB (e.g. schools, employers etc.) to provide psychosocial opportunity and care. Attention should be paid to the psychosocial impact of EB as well as physical needs. Directions for research are indicated. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13023-019-1086-5) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-6560722 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-65607222019-06-14 Psychosocial recommendations for the care of children and adults with epidermolysis bullosa and their family: evidence based guidelines Martin, K. Geuens, S. Asche, J. K. Bodan, R. Browne, F. Downe, A. García García, N. Jaega, G. Kennedy, B. Mauritz, P. J. Pérez, F. Soon, K. Zmazek, V. Mayre-Chilton, K. M. Orphanet J Rare Dis Review Epidermolysis Bullosa (EB) is a group of rare genetic disorders resulting in skin fragility and other symptoms. Commissioned by DEBRA International and funded by DEBRA Norway, this evidence-bases guideline provides recommendations to optimise psychosocial wellbeing in EB. An international multidisciplinary panel of social and health care professionals (HCP) and people living with EB was formed. A systematic international literature review was conducted by the panel following the Scottish Intercollegiate Guidelines Network (SIGN) methodology. The resulting papers underwent systematic selection and critique processes. Included papers were allocated to 6 different outcome groups to allow data synthesis and exploration: quality of life, coping, family, wellbeing, access to HCP and pain. Based on the evidence in those papers, recommendations were made for individuals living with EB, family and caregivers and HCP working in the field. Few studies have investigated interventions and which factors lead to better outcomes, but general recommendations can be made. EB is a complex disease impacting enormously on every aspect of psychosocial life. People and families living with EB need access to multidisciplinary support, including psychological guidance, in order to improve quality of life and psychosocial wellbeing. Interventions should stimulate social participation to prevent isolation. People with EB and their families should be able to access a supportive network. HCP should be well supported and educated about the complexity of EB. They should work collaboratively with those around the individual with EB (e.g. schools, employers etc.) to provide psychosocial opportunity and care. Attention should be paid to the psychosocial impact of EB as well as physical needs. Directions for research are indicated. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13023-019-1086-5) contains supplementary material, which is available to authorized users. BioMed Central 2019-06-11 /pmc/articles/PMC6560722/ /pubmed/31186066 http://dx.doi.org/10.1186/s13023-019-1086-5 Text en © The Author(s). 2019 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 | Review Martin, K. Geuens, S. Asche, J. K. Bodan, R. Browne, F. Downe, A. García García, N. Jaega, G. Kennedy, B. Mauritz, P. J. Pérez, F. Soon, K. Zmazek, V. Mayre-Chilton, K. M. Psychosocial recommendations for the care of children and adults with epidermolysis bullosa and their family: evidence based guidelines |
title | Psychosocial recommendations for the care of children and adults with epidermolysis bullosa and their family: evidence based guidelines |
title_full | Psychosocial recommendations for the care of children and adults with epidermolysis bullosa and their family: evidence based guidelines |
title_fullStr | Psychosocial recommendations for the care of children and adults with epidermolysis bullosa and their family: evidence based guidelines |
title_full_unstemmed | Psychosocial recommendations for the care of children and adults with epidermolysis bullosa and their family: evidence based guidelines |
title_short | Psychosocial recommendations for the care of children and adults with epidermolysis bullosa and their family: evidence based guidelines |
title_sort | psychosocial recommendations for the care of children and adults with epidermolysis bullosa and their family: evidence based guidelines |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6560722/ https://www.ncbi.nlm.nih.gov/pubmed/31186066 http://dx.doi.org/10.1186/s13023-019-1086-5 |
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