Assessing the needs of caregivers of children and adolescents with fetal alcohol spectrum disorders: Results from a survey among families and professionals in Germany.
Caregivers
FASD
Fetal alcohol syndrome
Health services research
Needs assessment
Journal
European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society
ISSN: 1532-2130
Titre abrégé: Eur J Paediatr Neurol
Pays: England
ID NLM: 9715169
Informations de publication
Date de publication:
Jul 2021
Jul 2021
Historique:
received:
08
12
2020
revised:
15
03
2021
accepted:
27
04
2021
pubmed:
11
5
2021
medline:
13
10
2021
entrez:
10
5
2021
Statut:
ppublish
Résumé
Caring for individuals with fetal alcohol spectrum disorders (FASD) puts a substantial and often life-long burden on affected families. Caregivers' specific needs and demands are, however, not well understood so far. We thus aimed at systematically collecting data on the needs of individuals caring for children and adolescents with FASD. Between May 2019 and November 2020, a quantitative survey among caregivers and professionals from across Germany was performed. Participants completed a questionnaire collecting information on the perceived support caregivers receive from various sources as well as the current fulfilment of caregivers' needs. Specifically, the fulfilment of a variety of specific needs summarised in five categories was rated by the participants on a scale ranging from 1 (very good) to 6 (insufficient). Both caregivers and professionals rated the overall fulfilment of needs rather poorly (mean: 3.94 and 4.27, respectively). Caregivers indicated needs concerning coordination of support (4.74) and relief services (4.44) to be fulfilled the least while needs in the relief services category also received the lowest average grade among professionals (4.57). The needs that the caregivers regarded as most sufficiently fulfilled were their own knowledge about FASD (mean: 1.95) and their knowledge about the causes of their child's problems (mean: 1.87). The results of the present study indicate that FASD caregivers are supported insufficiently, while most of their needs remain unmet. Health care planners and providers thus urgently need to identify and implement measures to better address FASD caregivers' needs and demands.
Identifiants
pubmed: 33971449
pii: S1090-3798(21)00094-5
doi: 10.1016/j.ejpn.2021.04.008
pii:
doi:
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
1-8Informations de copyright
Copyright © 2021 European Paediatric Neurology Society. Published by Elsevier Ltd. All rights reserved.
Déclaration de conflit d'intérêts
Declaration of competing interest The project ‘German Competence Centre Bavaria’ (Deutsches FASD KOMPETENZZENTRUM Bayern) within which the present study was performed receives financial support from the Bavarian State Ministry of Health and Care, the German Federal Ministry of Health, the private foundation Robert-Vogel-Stiftung (RVS), and the non-profit organisation Soziale Beratungs-und Betreuungsdienste (SBB) Bayern gGmbH. The funding bodies had no role in the study design, in the collection, analysis and interpretation of data, in the writing of the report, or in the decision to submit the article for publication. Apart from this funding, the authors declare no competing interests.