Literature DB >> 24950521

Discontinuity of care at end of life: a qualitative exploration of OOH end of life care.

Geraldine M Leydon1, Narinder K Shergill, Charles Campion-Smith, Helen Austin, Caroline Eyles, Jenny Baverstock, Julia Addington-Hall, Richard Sloan, Carol Davis, Michael V Moore.   

Abstract

OBJECTIVE: This study aimed to understand the experiences of palliative care patients when accessing or making decisions about out of hours (OOH) services. It also aimed to illuminate barriers and enablers to accessing appropriate and timely care following the introduction of the 2004 New General Medical Services Contract.
METHOD: Longitudinal prospective qualitative study using semi-structured interviews and telephone interviews over 6 months and analysed for thematic content. 32 patients defined as receiving palliative care in six General Practices and three hospices selected on the basis of size and rural/urban location in Southern England were recruited.
RESULTS: Continuity of care was highly valued. Participants described the importance of being known by the healthcare team, and the perceived positive implications continuity could have for the quality of care they received and the trust they had in their care. Various factors prevented participants from seeking help or advice from OOH services, despite having health concerns that may have benefitted from medical assistance. Prior poor experience, limited knowledge of services and knowing who to call and, indeed, when to call were all factors that reportedly shaped participants' use of OOH services.
CONCLUSIONS: Interpersonal or relationship continuity and management continuity are vital to the process of optimising the patient experience of OOH palliative care. While recent service innovations are tackling some of the issues highlighted, this research reinforces the value patients with palliative care needs places on continuity and the need to improve this aspect of care management.

Entities:  

Keywords:  Palliative; Qualitative

Mesh:

Year:  2013        PMID: 24950521     DOI: 10.1136/bmjspcare-2012-000266

Source DB:  PubMed          Journal:  BMJ Support Palliat Care        ISSN: 2045-435X            Impact factor:   3.568


  8 in total

1.  Events Leading to Hospital-Related Disenrollment of Home Hospice Patients: A Study of Primary Caregivers' Perspectives.

Authors:  Veerawat Phongtankuel; Shawn Paustian; Manney Carrington Reid; Amanda Finley; Angela Martin; John Delfs; Rosemary Baughn; Ronald D Adelman
Journal:  J Palliat Med       Date:  2016-11-28       Impact factor: 2.947

2.  Out-of-hours primary care use at the end of life: a descriptive study.

Authors:  Rebecca Fr Fisher; Daniel Lasserson; Gail Hayward
Journal:  Br J Gen Pract       Date:  2016-07-05       Impact factor: 5.386

3.  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

4.  Providing end-of-life care in general practice: findings of a national GP questionnaire survey.

Authors:  Sarah Mitchell; Joelle Loew; Catherine Millington-Sanders; Jeremy Dale
Journal:  Br J Gen Pract       Date:  2016-07-05       Impact factor: 5.386

5.  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

6.  Utilisation of after-hours telephone support in a home-based hospice service.

Authors:  Poh-Heng Chong; Jasmin Lee; Zhi-Zheng Yeo; Raymond Qishun Ang
Journal:  BMC Palliat Care       Date:  2022-09-16       Impact factor: 3.113

7.  Patient-provider disconnect: A qualitative exploration of understanding and perceptions to care integration.

Authors:  Yi Feng Lai; Andrew Yew Wai Lum; Emily Tse Lin Ho; Yee Wei Lim
Journal:  PLoS One       Date:  2017-10-27       Impact factor: 3.240

8.  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

  8 in total

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