How continuity of care is experienced within the context of integrated palliative care: A qualitative study with patients and family caregivers in five European countries

Author:

den Herder-van der Eerden Marlieke1,Hasselaar Jeroen1,Payne Sheila2,Varey Sandra2,Schwabe Sven3,Radbruch Lukas3,Van Beek Karen4,Menten Johan4,Busa Csilla5,Csikos Agnes5,Vissers Kris1,Groot Marieke1

Affiliation:

1. Department of Anesthesiology, Pain and Palliative Care, Radboud University Medical Center, Nijmegen, The Netherlands

2. Division of Health Research, International Observatory on End of Life Care, Lancaster University, Lancaster, UK

3. Klinik für Palliativmedizin, Universitätsklinikum Bonn, Bonn, Germany

4. Department of Radiation Oncology and Palliative Care, University Hospital Leuven, Leuven, Belgium

5. Department of Primary Health Care, Medical School, University of Pecs (UP), Pécs, Hungary

Abstract

Background: Patients with advanced diseases often experience deficient continuity of care. Although integrated palliative care promotes continuity of care, it is not clear how it can be optimized to improve continuity of care experiences. Aim: To examine how relational, informational and management continuity of care are experienced by patients with advanced diseases and their family caregivers receiving care from several integrated palliative care initiatives in five European countries. Design: We adopted a longitudinal qualitative study design including two interviews (interval 3 months) with patients and family caregivers focusing on how health care professionals responded to their needs. Interviews were audio-recorded and transcribed verbatim. Analysis involved a two-step qualitative content approach. Setting/participants: A total of 22 integrated palliative care initiatives (established local palliative care collaborations) were selected in Belgium, Germany, Hungary, the Netherlands and the United Kingdom. We recruited 152 patients (63% cancer, 24% chronic obstructive pulmonary disease, 13% heart failure; life expectancy <1 year; mean age 68 years, 56% female) and 92 family caregivers (mean age 61 years, 66% female). Results: Trusted relationships with a small number of key health care professionals to receive tailored care and easily access help were essential. Relational continuity was often deficient, especially with general practitioners. Although informational and management continuity was often lacking in care provision, collaborative integrated palliative care initiatives were related to consistent and coherent care. Conclusion: Patients and family caregivers most likely experience continuity of care by having a small number of trusted health care professionals who are available, provide multidisciplinary care and regularly transfer information to all health care professionals involved. Optimizing continuity of care requires further integration of integrated palliative care initiatives with other health care professionals involved in the patients’ care networks.

Publisher

SAGE Publications

Subject

Anesthesiology and Pain Medicine,General Medicine

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