Evidence map›Paper›PMID 41918215›Full record

ArticlePalliative & supportive care2026

A qualitative study exploring the pros and cons of universal pediatric palliative care referral at diagnosis for children with cancer.

Leeat Granek, S C M Veldhuijzen van Zanten, Dave Lysecki, Adam Rapoport, Natasha Datoo, Fyeza Hasan, Sumit Gupta, Lori Wiener, Kimberley Widger, Anthony Chan and 4 more

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Article in Palliative & supportive care, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Not yet cited in PubMed.

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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

14 authors.

Leeat GranekSchool of Health Policy and Management, York University, Toronto, Ontario, Canada.ORCID https://orcid.org/0000-0001-9936-2826
S C M Veldhuijzen van ZantenPalliative Care, Children's Hospital of Eastern Ontario, Toronto, Ontario, Canada.
Dave LyseckiDivision of Palliative Medicine, Department of Pediatrics, McMaster University, Toronto, Ontario, Canada.
Adam RapoportPaediatric Advanced Care Team, The Hospital for Sick Children, Toronto, Ontario, Canada.
Natasha DatooDivision of Haematology/Oncology, BC Children's Hospital, Toronto, Ontario, Canada.
Fyeza HasanDivision of Haematology/Oncology, Hospital for Sick Children, Toronto, Ontario, Canada.
Sumit GuptaDivision of Haematology/Oncology, Hospital for Sick Children, Toronto, Ontario, Canada.
Lori WienerCenter for Cancer Research, National Cancer Institute, NIH, Toronto, Ontario, USA.ORCID https://orcid.org/0000-0002-9573-8870
Kimberley WidgerLawrence Bloomberg Faculty of Nursing, University of Toronto, Toronto, Ontario, Canada.
Anthony ChanDivision of Palliative Medicine, Department of Pediatrics, McMaster University, Toronto, Ontario, Canada.
Alisha KassamDepartment of Paediatrics, Southlake Hospital, Toronto, Ontario, Canada.
Karen FergusDepartment of Psychology, Faculty of Health, York University, Toronto, Ontario, Canada.
Emily McCulloghSchool of Health Policy and Management, York University, Toronto, Ontario, Canada.
Donna JohnstonDivision of Haematology/Oncology, Children's Hospital of Eastern Ontario, Toronto, Ontario, Canada.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundEarly integration of pediatric palliative care (PPC) offers significant benefits for children with cancer, yet referrals often occur late in the child's cancer trajectory.

objectivesAs part of a larger project looking at barriers and facilitators to early integration of PPC, this study explored the perspectives of healthcare providers (HCPs) on the pros and cons of a universal referral system where all children with cancer are referred to PPC at diagnosis.

methodsUsing the grounded theory method, semi-structured interviews were conducted with 66 oncology and PPC providers across 4 tertiary cancer centers in Canada. Interviews were coded line-by-line to explore patterns and themes across the dataset.

resultsThree key benefits emerged that included: reducing stigma and normalizing PPC as standard care, fostering early relationship building with patients and families, and minimizing HCP subjectivity in making PPC referrals. Cons included the idea that universal referral was a poor use of resources, particularly for children with curable cancers, and that this system lacked usefulness for patients and families. SIGNIFICANCE OF

resultsUniversal referral can promote equitable, timely, and family-centered integration of PPC in pediatric oncology. However, these types of referral systems face substantial challenges, particularly around resources. There was also wide variation of opinions and acceptability of universal referral among providers. The adoption of standardized or tiered referral criteria, guided by disease risk, prognosis, or symptom burden, may represent a practical middle ground. Future work should evaluate the impact of such criteria-based referral models on patient and family outcomes, provider experiences, and healthcare resource use.

Indexed as

NeoplasmsPalliative CarePediatricsReferral and ConsultationCanadaChildFemaleGrounded TheoryHumansInterviews as TopicMaleQualitative Researchchildcommunicationhealth personnelneoplasmsPalliative carepatient referralqualitative researchsymptom managementterminal care

Identifiers

PMID41918215
PMCPMC13166708

What OpenQuestion holds

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LicenceCC BY
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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.