Intersectoral collaboration in home-based end-of-life pediatric cancer care: A qualitative multiple-case study integrating families’ and professionals’ experiences

Author:

Hammer Nanna Maria12ORCID,Hansson Helena12,Pedersen Line Hjøllund13ORCID,Abitz Maja1,Sjøgren Per4,Schmiegelow Kjeld12,Bidstrup Pernille Envold56,Larsen Hanne Bækgaard12,Olsen Marianne17

Affiliation:

1. Department of Paediatrics and Adolescent Medicine, Copenhagen University Hospital - Rigshospitalet, Copenhagen, Denmark

2. Department of Clinical Medicine, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark

3. Survivorship and Inequality in Cancer, Danish Cancer Society Research Center, Copenhagen, Denmark

4. Department of Oncology, Copenhagen University Hospital - Rigshospitalet, Copenhagen, Denmark

5. Psychological Aspects of Cancer, Danish Cancer Society Research Center, Copenhagen, Denmark

6. Institute of Psychology, University of Copenhagen, Copenhagen, Denmark

7. Department of Pediatrics and Adolescent Medicine, Section of Pediatric Hematology and Oncology, Aalborg University Hospital, Aalborg, Denmark

Abstract

Background:Many children and adolescents with incurable cancer and their families prefer to receive end-of-life care and to die at home. This implies a transition of care from hospital to home and presupposes the establishment of a well-functioning collaboration between the family and professionals across health care sectors.Aim:To identify and explore key elements of home-based end-of-life care collaboration for children with cancer, as experienced by their parents and grandparents and the hospital- and community-based professionals involved.Design:Descriptive qualitative multiple-case study. Data were collected by semi-structured interviews and written responses to open-ended questions, and analyzed inductively across cases using qualitative content analysis.Setting/participants:Cases comprised a criterion sample of five children (aged <18 years), who died of cancer at home. Cases were represented by the children’s bereaved parents ( n = 8) and grandparents ( n = 7), and community-based professionals ( n = 16). Also, hospital-based professionals ( n = 10) were interviewed about the children’s end-of-life care through group interviews.Results:We identified five main themes, describing key elements of the end-of-life collaboration: Establishing the collaboration, Bolstering family life, Elucidating organization and integration, Managing challenges, and Closing the collaboration. These themes all came under the overarching theme: A mutual trust-based collaboration. On this basis, we developed the “Home-Based Pediatric End-of-Life Care Model for Children with Cancer.”Conclusions:By highlighting key elements in the family-centered, intersectoral and interprofessional end-of-life care collaboration, our “Home-Based Pediatric End-of-Life Care Model for Children with Cancer” offers a framework for further optimization of home-based end-of-life care services for children with cancer and their families.

Funder

Tømrermester Jørgen Holm og Hustru Elisa f. Hansens Mindelegat

Kræftens Bekæmpelse

Helsefonden

Axel Muusfeldts Fond

Dagmar Marshalls Fond

Publisher

SAGE Publications

Subject

Anesthesiology and Pain Medicine,General Medicine

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