Literature DB >> 21427205

Caring for children dying from cancer at home: a qualitative study of the experience of primary care practitioners.

Sue J Neilson1, Joe Kai, Christine Macarthur, Sheila M Greenfield.   

Abstract

BACKGROUND: The rarity of childhood cancers makes providing palliative care in the community an unusual event for primary care practitioners. Providing this care requires effective inter-professional collaboration with the team that forms to provide the care often working together for the first and only time.
OBJECTIVE: To explore the experiences of primary care practitioners following their involvement in the palliative care of a child with cancer at home.
METHODS: The study design was a community-based qualitative study. The study location was the West Midlands region. Purposeful sample of GPs and community nurses involved in providing palliative care to 12 children. One-to-one in-depth interviews with 47 primary care professionals (10 GPs and 37 community nurses) and 5 facilitated case discussions were undertaken. Field notes were documented and grounded theory data analysis undertaken: chronological comparative data analysis identifying generated themes.
RESULTS: GPs had minimal input into the preceding care of children undergoing treatment for cancer but sought to re-establish their role at the child's transition to palliative care. GPs felt they had a role to play and could add value to this phase of care, highlighted their continuing role with the child's family and acknowledged that they had gained from the experience of contributing. However, lack of specialist knowledge and uncertainty about their role within the team made this more challenging. In contrast, community nurses were routinely involved in both active treatment and palliation care phases. There was little evidence of collaboration between the specialist and primary care professionals involved. There was considerable variation in out of hours provision across cases.
CONCLUSIONS: Engaging primary care practitioners needs to be more actively anticipated and negotiated at the transition to palliation. Variation in out of hours care is another cause for concern. Enhancing inter-professional collaboration and planning during both active and palliative care phases may help.

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Year:  2011        PMID: 21427205     DOI: 10.1093/fampra/cmr007

Source DB:  PubMed          Journal:  Fam Pract        ISSN: 0263-2136            Impact factor:   2.267


  4 in total

Review 1.  The role of the GP in follow-up cancer care: a systematic literature review.

Authors:  Judith A Meiklejohn; Alexander Mimery; Jennifer H Martin; Ross Bailie; Gail Garvey; Euan T Walpole; Jon Adams; Daniel Williamson; Patricia C Valery
Journal:  J Cancer Surviv       Date:  2016-05-02       Impact factor: 4.442

2.  Staff Efficiency Trends Among Pediatric Hospices, 2002-2011.

Authors:  Melanie J Cozad; Lisa C Lindley; Sandra J Mixer
Journal:  Nurs Econ       Date:  2016 Mar-Apr       Impact factor: 1.085

3.  Pediatric Oncology Palliative Care: Experiences of General Practitioners and Bereaved Parents.

Authors:  Sue J Neilson; Faith Gibson; Sheila M Greenfield
Journal:  J Palliat Care Med       Date:  2015-03-01

4.  Children with cancer: a survey on the experience of Italian primary care pediatricians.

Authors:  Marta Minute; Giorgio Cozzi; Chiara Plotti; Giuseppe Montanari; Paolo Pecile; Giulio Andrea Zanazzo; Alessandro Ventura; Egidio Barbi
Journal:  Ital J Pediatr       Date:  2017-05-25       Impact factor: 2.638

  4 in total

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