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When a child dies: parents' experiences of palliative care-an integrative literature review.
Mittuniversitetet.ORCID iD: 0000-0001-9623-5813
2014 (English)In: Journal of Pediatric Nursing: Nursing Care of Children and Families, ISSN 0882-5963, E-ISSN 1532-8449, Vol. 29, no 6, p. 660-9, article id S0882-5963(14)00192-4Article in journal (Refereed) Published
Abstract [en]

The aim of this integrative review was to increase knowledge about parents' experiences of palliative care when their child is dying or has died due to illness using Whittemore and Knafl (2005) analysis process. Computerized databases were used to search the literature. Nine papers met the inclusion criteria. The analysis resulted in five categories: genuine communication, sincere relationships, respect as an expert, and alleviation of suffering and need of support, including 15 subcategories. Health professionals need education to provide high-quality pediatric palliative care. They especially need training concerning existential issues, and further studies need to be performed.

Place, publisher, year, edition, pages
2014. Vol. 29, no 6, p. 660-9, article id S0882-5963(14)00192-4
Keywords [en]
Communication, Family, Literature review, Palliative care, Pediatrics, Support
National Category
Nursing
Identifiers
URN: urn:nbn:se:esh:diva-7422DOI: 10.1016/j.pedn.2014.06.009PubMedID: 25038375OAI: oai:DiVA.org:esh-7422DiVA, id: diva2:1305409
Available from: 2019-04-16 Created: 2019-04-16 Last updated: 2019-04-17Bibliographically approved

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Melin-Johansson, Christina
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