Telephone advice lines for adults with advanced illness and their family carers: a qualitative analysis and novel practical framework

Author:

Pask Sophie12ORCID,Omoruyi Allen1,Mohamed Ahmed1,Chambers Rachel L2ORCID,McFarlane Phillippa G2ORCID,Johansson Therese2ORCID,Kumar Rashmi2,Woodhead Andy2,Okamoto Ikumi3,Barclay Stephen3,Higginson Irene J24ORCID,Sleeman Katherine E24ORCID,Murtagh Fliss EM12ORCID

Affiliation:

1. Wolfson Palliative Care Research Centre, Hull York Medical School, University of Hull, Hull, UK

2. Cicely Saunders Institute of Palliative Care, Policy & Rehabilitation, King’s College London, London, UK

3. Department of Public Health and Primary Care, University of Cambridge, Cambridge, UK

4. King’s College Hospital NHS Foundation Trust, London, UK

Abstract

Background: Telephone advice lines have been recommended internationally to support around-the-clock care for people living at home with advanced illness. While they undoubtedly support care, there is little evidence about what elements are needed for success. A national picture is needed to understand, improve and standardise service delivery/care. Aim: To explore telephone advice lines for people living at home with advanced illness across the four UK nations, and to construct a practical framework to improve services. Design: A cross-national evaluation of telephone advice lines using structured qualitative interviews. A patient and public involvement workshop was conducted to refine the framework. Setting/participants: Professionals with responsibilities for how palliative care services are delivered and/or funded at a local or regional level, were purposively sampled. Results: Seventy-one interviews were conducted, covering 60 geographical areas. Five themes were identified. Availability: Ten advice line models were described. Variation led to confusion about who to call and when. Accessibility, awareness and promotion: It was assumed that patients/carers know who to call out-of-hours, but often they did not. Practicalities: Call handlers skills/expertise varied, which influenced how calls were managed. Possible responses ranged from signposting to organising home visits. Integration/continuity of care: Integration between care providers was limited by electronic medical records access/information sharing. Service structure/commissioning: Sustained funding was often an issue for charitably funded organisations. Conclusions: Our novel evidence-based practical framework could be transformative for service design/delivery, as it presents key considerations relating to the various elements of advice lines that may impact on the patient/carer experience.

Funder

Marie Curie

Publisher

SAGE Publications

Reference65 articles.

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