Inter-Professional Caring for Children Who Are Relatives of Cancer Patients in Palliative Care: Perspectives of Doctors and Social Workers.

A palliative cancer diagnosis in a parent has a major impact on many aspects of patients' children. This article aims to explore how doctors and social workers met children as relatives of a parent with cancer in order to understand the possibilities and difficulties in supporting children in specia...

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Published in:British Journal of Social Work Vol. 49; no. 3; pp. 595 - 615
Main Authors: Karidar, Hakima, Glasdam, Stinne
Format: research tables/charts Journal Article
Published: Oxford University Press / USA Apr2019
Online Access:View this record in EBSCOhost
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      dt: Apr2019
      vid: 49
      iid: 3
      pid: 622
      pub: Oxford University Press / USA
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        136161057
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        10.1093/bjsw/bcy080
        136161057
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        atl: Inter-Professional Caring for Children Who Are Relatives of Cancer Patients in Palliative Care: Perspectives of Doctors and Social Workers.
      aug:
        au:
          Karidar, Hakima
          Glasdam, Stinne
        affil: Integrative Health Research, Department of Health Sciences, Lund University, Lund, Sweden
      sug:
        subj:
          Neoplasms
          Support, Psychosocial
          Physician Attitudes
          Social Worker Attitudes
          Interprofessional Relations
          Professional-Family Relations
          Human
          Sweden
          Semi-Structured Interview
          Family
          Palliative Care
          Physicians
          Social Workers
          Conceptual Framework
          Child
          Meetings
          Collaboration
          Professional Role
          Parent-Child Relations
          Child Welfare
          Access to Information
          Child: 6-12 years
      ab: A palliative cancer diagnosis in a parent has a major impact on many aspects of patients' children. This article aims to explore how doctors and social workers met children as relatives of a parent with cancer in order to understand the possibilities and difficulties in supporting children in specialised palliative homecare in Sweden. Qualitative, semi-structured interviews of doctors and social workers were conducted, inspired by Bourdieu. The findings showed that professionals had limited contact with patients' children. Mono- and inter-professional meetings were organising structures for working days of doctors and social workers. Due to hierarchy positions, doctors often set the agenda in inter-professional teamwork. Doctors seldom met patients' children, only when information about parents' cancer diseases were needed. Social workers were responsible for psycho-social issues, but mostly only special vulnerable families and their children were prioritised. Meetings between children and professionals were conditional on the parents' permission and, even if permission was given, meetings seldom took place. Doctors and social workers were subject to the structural frame and a medical logic, which limited their interactions with children of the patients. Children were dependent on both their parents and professionals, who had the power to include or exclude them from parents' illness situation.
      pubtype: Academic Journal
      doctype:
        research
        tables/charts
        Journal Article
      ougenre: Article
    language: English
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