• Palliative medicine · Apr 2018

    Patients' and carers' perspectives of palliative care in general practice: A systematic review with narrative synthesis.

    • Emilie Green, Selena Knight, Merryn Gott, Stephen Barclay, and Patrick White.
    • 1 Department of Primary Care & Public Health Sciences, Division of Health & Social Care Research, King's College London, London, UK.
    • Palliat Med. 2018 Apr 1; 32 (4): 838-850.

    BackgroundGeneral practitioners have overall responsibility for community care, including towards end of life. Current policy places generalists at the centre of palliative care provision. However, little is known about how patients and carers understand the general practitioner's role.AimsTo explore patient and carer perspectives of (1) the role of the general practitioner in providing palliative care to adult patients and (2) the facilitators and barriers to the general practitioner's capacity to fulfil this perceived role.DesignSystematic literature review and narrative synthesis.Data SourcesSeven electronic databases (MEDLINE, Embase, PsycINFO, BNI, CINAHL, Cochrane and HMIC) were searched from inception to May 2017. Two reviewers independently screened papers at title, abstract and full-text stages. Grey literature, guideline, hand searches of five journals and reference list/citation searches of included papers were undertaken. Data were extracted, tabulated and synthesised using narrative, thematic analysis.ResultsA total of 25 studies were included: 14 employed qualitative methods, 8 quantitative survey methods and 3 mixed-methods. Five key themes were identified: continuity of care, communication between primary and secondary care, contact and accessibility, communication between general practitioner and patient, and knowledge and competence.ConclusionAlthough the terminology and context of general practice vary internationally, themes relating to the perceived role of general practitioners were consistent. General practitioners are considered well placed to provide palliative care due to their breadth of clinical responsibility, ongoing relationships with patients and families, and duty to visit patients at home and coordinate healthcare resources. These factors, valued by service users, should influence future practice and policy development.

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