Golla, Heidrun, Mammeas, Stephanie, Galushko, Maren, Pfaff, Holger ORCID: 0000-0001-9154-6575 and Voltz, Raymond (2015). Unmet needs of caregivers of severely affected multiple sclerosis patients: A qualitative study. Palliat. Support Care, 13 (6). S. 1685 - 1694. NEW YORK: CAMBRIDGE UNIV PRESS. ISSN 1478-9523

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Abstract

Objective: Multiple sclerosis (MS) patients' caregivers are sometimes considered as hidden patients. How much more this might be true for caregivers of severely affected MS patients has so far been scarcely studied. Palliative care also addressing relatives' needs might therefore be very relevant for these caregivers. However, we do not yet know which unmet needs they have and how these could be met. Our aim was to gain an insight into the subjectively unmet needs of caregivers of severely affected MS patients in Germany. Method: The study employed a qualitative cross-sectional approach for assessing unmet needs. Twelve caregivers of severely affected MS patients were recruited using a convenience sampling approach. Face-to-face interviews were conducted, audiotaped, and transcribed verbatim, followed by qualitative content analysis. Results: Unmet needs were sorted into the following categories: relationship to physician, individual support by the healthcare system, relationship to the individual severely affected by MS, end-of-life issues, self-care, and higher awareness of MS. Caregivers tended to group the unmet needs of their care recipients with their own and rarely focused on their own wishes and restrictions. Significance of Results: A close patient-caregiver dyad makes it difficult to differentiate unmet caregiver needs. However, the palliative care approach might help caregivers of severely affected MS patients by answering questions on disease progress and end-of-life issues, as well as by offering respite care, support for self-care, and help in preserving one's identity, and also anticipating the time to come after the death.

Item Type: Journal Article
Creators:
CreatorsEmailORCIDORCID Put Code
Golla, HeidrunUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Mammeas, StephanieUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Galushko, MarenUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Pfaff, HolgerUNSPECIFIEDorcid.org/0000-0001-9154-6575UNSPECIFIED
Voltz, RaymondUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
URN: urn:nbn:de:hbz:38-385479
DOI: 10.1017/S1478951515000607
Journal or Publication Title: Palliat. Support Care
Volume: 13
Number: 6
Page Range: S. 1685 - 1694
Date: 2015
Publisher: CAMBRIDGE UNIV PRESS
Place of Publication: NEW YORK
ISSN: 1478-9523
Language: English
Faculty: Unspecified
Divisions: Unspecified
Subjects: no entry
Uncontrolled Keywords:
KeywordsLanguage
PALLIATIVE CARE NEEDS; OF-LIFE; HEALTH-PROFESSIONALS; PEOPLE; EXPERIENCES; BURDEN; IMPACT; CONSEQUENCES; INDIVIDUALS; PARTNERSMultiple languages
Health Policy & ServicesMultiple languages
URI: http://kups.ub.uni-koeln.de/id/eprint/38547

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