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ABSTRACT: Aims
The aims of this review were: (1) to obtain an overview of caregiver-reported information needs; and (2) to investigate if there are information needs that are unique for caregivers of persons with rare epilepsies.Method
We followed the scoping review framework outlined by Arksey and O'Malley and the preferred reporting items outlined by PRISMA.Results
Among the 17 articles that met the inclusion criteria, 5 included caregivers of persons with rare epilepsies. Categories of information needs: (1) Medical information; (2) Information on how to cope with emotional distress; (3) Experiential information from peers; and (4) Interdisciplinary information exchange. The need for disorder-specific information seemed particularly important for caregivers of persons with rare epilepsies.Conclusion
There is a need for further studies, particularly on formal caregivers' information needs.
SUBMITTER: Tschamper MK
PROVIDER: S-EPMC9442773 | biostudies-literature | 2022 Sep
REPOSITORIES: biostudies-literature
Tschamper Merete Kristin MK Systad Silje S
Journal of intellectual disabilities : JOID 20210517 3
<h4>Aims</h4>The aims of this review were: (1) to obtain an overview of caregiver-reported information needs; and (2) to investigate if there are information needs that are unique for caregivers of persons with rare epilepsies.<h4>Method</h4>We followed the scoping review framework outlined by Arksey and O'Malley and the preferred reporting items outlined by PRISMA.<h4>Results</h4>Among the 17 articles that met the inclusion criteria, 5 included caregivers of persons with rare epilepsies. Catego ...[more]