Evidence map›Paper›PMID 40500254›Full record

ArticleInternational journal of qualitative studies on health and well-being2025

What matters to patients with cancer receiving home care at the end of life? A qualitative study comparing patients' and healthcare professionals' views.

Lisbeth Thoresen, Eline Aas, Nikki McCaffrey, Lidia Engel, Nina Løkkevik, Yvonne Anne Michel, Gudrun Maria Waaler Bjørnelv

Abstract readComparative Study
In one paragraph

Article in International journal of qualitative studies on health and well-being, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Lisbeth ThoresenDepartment for Interdisciplinary Health Science, Faculty of Medicine, University of Oslo, Oslo, Norway.ORCID 0000-0003-3617-9770
Eline AasDepartment of Health Management and Health Economics, University of Oslo, Oslo, Norway.ORCID 0000-0002-9878-6165
Nikki McCaffreyDeakin Health Economics, School of Health & Social Development, Institute for Health Transformation, Faculty of Health, Deakin University, Burwood, Australia.ORCID 0000-0003-3684-3723
Lidia EngelHealth Economics Group, School of Public Health and Preventive Medicine, Monash University, Melbourne, Australia.ORCID 0000-0002-7959-3149
Nina LøkkevikResearch and Development Department, Moss, Norway.
Yvonne Anne MichelFaculty of Social Sciences, University of Applied Sciences Zittau/Görlitz, Görlitz, Germany.ORCID 0009-0002-4133-654X
Gudrun Maria Waaler BjørnelvDepartment of Health Management and Health Economics, University of Oslo, Oslo, Norway.ORCID 0000-0003-4997-5426

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeTo improve care for patients in the last phase of life, healthcare professionals (HCPs) need to understand what matters to them in terms of care and follow-up. Therefore, in our study, we investigated how patients with cancer in Norway who are receiving home care perceive their situations and what matters to them at the end of life and compared it with HCPs' views on what matters to such patients.

methodsFollowing a qualitative design, we conducted in-depth interviews with eight patients with late-stage cancer living at home and four focus group interviews with 21 hCPs, mainly nurses. Patients and HCPs were recruited from two municipalities in Southeast and mid-Norway. The study period lasted from December 2020 to October 2022. We performed reflexive, thematic analyses of both data sets.

resultsThe views of all eight patients and all 21 hCPs were interpreted according to five themes: cancer impacts all aspects of life, navigating the healthcare system, living with dying, the paramount importance of relationships, and dying at home.

conclusionEntering the end of life, patients feel exhausted, lonely, and abandoned. They lack confidence in HCPs and the healthcare system. HCPs characterized plans and predictability as being important during end-of-life care, whereas patients were often hesitant to talk about and plan for the last phase of life.

Indexed as

Attitude of Health PersonnelHealth PersonnelHome Care ServicesNeoplasmsTerminal CareAdultAgedAged, 80 and overFemaleFocus GroupsHumansMaleMiddle AgedNorwayQualitative ResearchCancerend-of-life carehealthcare professionalhome carepatients’ experiencequalitative

Identifiers

PMID40500254
PMCPMC12160323

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.