Literature DB >> 21457601

The experiences and needs of people seeking palliative health care out-of-hours: a qualitative study.

Suzanne H Richards1, Rachel Winder, Clare Seamark, David Seamark, Sarah Avery, James Gilbert, Angela Barwick, John L Campbell.   

Abstract

AIM: To explore the experiences of people with advanced cancer and/or their caregivers accessing out-of-hours care.
BACKGROUND: The organisation and delivery of out-of-hours in the United Kingdom has undergone major reforms over the past three decades culminating in the new General Medical Service contract in 2004. There are concerns around continuity of care for patients with complex needs under the new arrangements.
DESIGN: A qualitative interview study was undertaken recruiting patients from two primary care trusts in Southwest England. Semi-structured interviews were conducted with 28 people with advanced cancer and/or their caregivers who had recently requested out-of-hours care. Interviews were recorded, transcribed and analysed thematically.
FINDINGS: Two main themes were identified including the legitimacy of seeking help and continuities of care. Most participants were reluctant to seek help, finding it difficult to decide whether their needs were sufficient to contact services. The degree to which services legitimised participants' requests mediated their experiences. Distress arose when services were dismissive of their needs, whereas respondents were appreciative of clinicians who provided them with reassurance. Participants reported a lack of relational and informational continuity of care. Consulting with an unfamiliar clinician out-of-hours raised doubts in some participants' minds about the quality of care. Some participants recounted episodes in which there were problems with pain management. While the themes suggest that the delivery of out-of-hours care as a whole was not always perfect, around-the-clock access to professional sources of support and reassurance was highly valued. However, the transfer of information to out-of-hours providers remains a key challenge; participants did not understand why out-of-hours providers could not access more information on their medical histories given the level of computerisation within the National Health Service. The findings highlight the need to improve continuity between in-hours and out-of-hours services for patients with complex needs.

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Year:  2011        PMID: 21457601     DOI: 10.1017/S1463423610000459

Source DB:  PubMed          Journal:  Prim Health Care Res Dev        ISSN: 1463-4236            Impact factor:   1.458


  6 in total

1.  Utilising out-of-hours primary care for assistance with cancer pain: a semi-structured interview study of patient and caregiver experiences.

Authors:  Rosalind Adam; Maria Giatsi Clausen; Susan Hall; Peter Murchie
Journal:  Br J Gen Pract       Date:  2015-11       Impact factor: 5.386

2.  Dying at home: a qualitative study of family carers' views of support provided by GPs community staff.

Authors:  David Seamark; Susan Blake; Sarah G Brearley; Christine Milligan; Carol Thomas; Mary Turner; Xu Wang; Sheila Payne
Journal:  Br J Gen Pract       Date:  2014-12       Impact factor: 5.386

3.  Impact of informational and relational continuity for people with palliative care needs: a mixed methods rapid review.

Authors:  Briony F Hudson; Sabine Best; Patrick Stone; Thomas Bill Noble
Journal:  BMJ Open       Date:  2019-05-29       Impact factor: 2.692

4.  An Innovative Approach for Improving Information Exchange between Palliative Care Providers in Slovenian Primary Health-A Qualitative Analysis of Testing a New Tool.

Authors:  Erika Zelko; Jozica Ramsak Pajk; Nevenka Krčevski Škvarč
Journal:  Healthcare (Basel)       Date:  2022-01-22

Review 5.  Barriers to palliative care in sexual and gender minority patients with cancer: A scoping review of the literature.

Authors:  Kelly Haviland; Chasity Burrows Walters; Susan Newman
Journal:  Health Soc Care Community       Date:  2020-08-07

6.  Impact of electronic palliative care coordination systems (EPaCCS) on care at the end of life across multiple care sectors, in one clinical commissioning group area, in England: a realist evaluation protocol.

Authors:  Lucy Pocock; Lydia French; Michelle Farr; Richard Morris; Sarah Purdy
Journal:  BMJ Open       Date:  2020-03-31       Impact factor: 2.692

  6 in total

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