Evidence map›Paper›PMID 41225466›Full record

ArticleBMC palliative care2025

"We're teetering on unsteady ground" parents' experiences of accessing 24/7 paediatric end-of-life care: a qualitative study.

Laura Barrett, Lorna Fraser, Lucy Ziegler, Stuart Jarvis, Susan Picton, Julia Hackett

Abstract read
In one paragraph

Article in BMC palliative care, 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.

Laura BarrettPaediatric Palliative Care Research Group, Department of Health Science, University of York, York, UK. Laura.barrett@york.ac.uk.ORCID http://orcid.org/0000-0001-8721-8886
Lorna FraserCicely Saunders Institute, Dept of Women's and Children's Health, King's College London, London, UK.ORCID http://orcid.org/0000-0002-1360-4191
Lucy ZieglerAcademic Unit of Palliative Care, University of Leeds, Clarendon Way, Leeds, UK.ORCID http://orcid.org/0000-0001-9563-5014
Stuart JarvisPaediatric Palliative Care Research Group, Department of Health Science, University of York, York, UK.ORCID http://orcid.org/0000-0001-8447-0306
Susan PictonLeeds Teaching Hospitals NHS Trust, Beckett Street, Leeds, UK.
Julia HackettCicely Saunders Institute, Dept of Women's and Children's Health, King's College London, London, UK.ORCID http://orcid.org/0000-0003-1720-6665

Funding

Marie Curie MC-21-805
6 · The paper itself

Abstract

backgroundProviding high quality around-the-clock care, is key to supporting families in their preferred place of care. Changing symptoms and parents' distress cannot wait for 'opening hours'. Yet in the UK, 24/7 children's end-of-life care remains a significant postcode lottery. To inform equitable service development this study explored parents' experiences accessing 24/7 paediatric palliative care, their expectations and needs.

methodsQualitative study using in-depth interviews, analysed using thematic analysis. Parents in one region of England, were eligible if their child had a life-limiting condition and end-of-life care was planned, or if they were bereaved parents whose child had died within the previous 3-36 months.

resultsTwenty-six parents were interviewed, 13 currently caring for their child and 13 bereaved parents. Two themes were developed: "Scaffolded for uncertainty and crisis" and "Falling through the service gaps". Most parents want seamless 24/7 end-of-life care for their child at home and to avoid hospital admissions. Despite being desperate to be home and feeling unsafe in hospital, service gaps mean, for some families, there is no option other than their child dying as an inpatient.

conclusionThe study found marked inequity in parent's experiences. Parents are confident when supported by a trusted 24/7 team with experience delivering palliative care, that provides phone support, face-to-face nursing and access to specialist advice. Hospital staff need improved training and consistent support from specialist palliative care teams. Further research with professionals is needed to understand the local and regional barriers that are preventing this support being available to all families.

Indexed as

Health Services AccessibilityParentsPediatricsTerminal CareAdultChildChild, PreschoolEnglandFemaleHumansInfantInterviews as TopicMaleMiddle AgedPalliative CareQualitative ResearchCare pathwaysGuidelinesPaediatric care servicesPaediatric end of life carePalliative careQualitative research

Identifiers

PMID41225466
PMCPMC12613421

What OpenQuestion holds

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Registered trials

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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.