Evidence map›Paper›PMID 40457393›Full record

ArticleBMC medical ethics2025

Mapping ethical issues encompassing end-of-life care for persons experiencing severe and persistent mental illness: a qualitative study.

Loïc Moureau, Monica Verhofstadt, Caressa Van Hoe, Joris Vandenberghe, Chantal Van Audenhove, Axel Liégeois

Abstract read
In one paragraph

Article in BMC medical ethics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

Loïc MoureauFaculty of Theology and Religious Studies, KU Leuven, Sint-Michielsstraat 4 bus 3100, Leuven, Belgium. loic.moureau@kuleuven.be.
Monica VerhofstadtFaculty of Medicine, UGent, Gent, Belgium.
Caressa Van HoeFaculty of Theology and Religious Studies, KU Leuven, Sint-Michielsstraat 4 bus 3100, Leuven, Belgium.
Joris VandenbergheFaculty of Medicine, KU Leuven, Leuven, Belgium.
Chantal Van AudenhoveFaculty of Medicine, KU Leuven, Leuven, Belgium.
Axel LiégeoisFaculty of Theology and Religious Studies, KU Leuven, Sint-Michielsstraat 4 bus 3100, Leuven, Belgium.

Funding

the KU Leuven Special Research Fund (BOF) grant number: ebc7b31d-c18d-4d94-9639-cfdb561abcdf
6 · The paper itself

Abstract

backgroundPersons experiencing severe and persistent mental illness (SPMI) represent a small but vulnerable group in mental health care and society. Research on this population is limited, despite significant ethical challenges in their care. These challenges include the severity of their illness, limited social networks, communication difficulties, impaired decision-making capacity, and, at times, disruptive behavior. PURPOSE: This study aims to explore the ethical themes that emerge in the care of persons experiencing SPMI, both in general and at the end of life. Specifically, we examine which issues arise, how care teams address ethical dilemmas, who is involved in decision-making, and what ethical frameworks or practices are utilized.

methodsWe conducted 73 in-depth qualitative interviews with care users, family members, caregivers, care managers, and experts from the Flemish region of Belgium. The data were analyzed through content analysis to identify recurring themes and reflect on ethical practices.

resultsThe findings reveal that while many facilities have ethical guidelines or advisory structures such as ethics committees, these are often not well known or not perceived as easily accessible to frontline staff. Ethical dilemmas are predominantly addressed at the team level, with some organizations employing a reference person ethics in the unit, "ethics pubs", or peer support mechanisms for challenging situations. The most frequently mentioned ethical issue was euthanasia, whereas others included neglect in home settings, prolonged delays in initiating palliative care, and maintaining autonomy for care users. Resource allocation, both at the organizational and societal levels, was also identified as an ethical concern. Caregivers described tensions between creative, individualized care and institutional policies, whereas families emphasized the shared responsibility in finding appropriate care.

conclusionEthical care for persons experiencing SPMI demands attention to autonomy, collaboration, and resource distribution. Greater accessibility to ethical support systems and tailored approaches are needed to balance recovery-oriented care with a palliative care approach, ensuring dignity and respect for this vulnerable group. CLINICAL TRIAL NUMBER: Not applicable.

Indexed as

Decision MakingMental DisordersTerminal CareAdultAgedBelgiumCaregiversFamilyFemaleHumansMaleMiddle AgedPalliative CareQualitative ResearchSocial SupportEnd-of-life careEthicsSevere and persistent mental illness (SPMI)

Identifiers

PMID40457393
PMCPMC12128549

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

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.