Evidence map›Paper›PMID 37344570›Full record

ArticleEuropean journal of human genetics : EJHG2024

A survey of genetic and palliative care health professionals' views of integrating genetics into palliative care.

Stephanie White, Erin Turbitt, Kris Rogers, Kathy Tucker, Alison McEwen, Megan Best, Jane L Phillips, Chris Jacobs

Open access · hybridAbstract read
In one paragraph

Article in European journal of human genetics : EJHG, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
1.6field-weighted citation impact, top 15% of its field
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

2 citing papers in PubMed, 5 citations in OpenAlex.

  1. Article
  2. Managing genetic information sharing at family and population level.European journal of human genetics : EJHG · 2024
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors at 4 institutions in 1 country.

Stephanie WhiteGraduate School of Health, University of Technology Sydney, Ultimo, NSW, Australia. stephanie.white@uts.edu.au.ORCID 0000-0002-5550-6397
Erin TurbittGraduate School of Health, University of Technology Sydney, Ultimo, NSW, Australia.ORCID 0000-0002-6650-9702
Kris RogersGraduate School of Health, University of Technology Sydney, Ultimo, NSW, Australia.
Kathy TuckerHereditary Cancer Centre, Nelune Comprehensive Cancer Centre, Prince of Wales Hospital, Randwick, NSW, Australia.ORCID 0000-0002-7180-6576
Alison McEwenGraduate School of Health, University of Technology Sydney, Ultimo, NSW, Australia.ORCID 0000-0001-8705-1190
Megan BestInstitute for Ethics and Society, University of Notre Dame Australia, Sydney, NSW, Australia.ORCID 0000-0003-1570-8872
Jane L PhillipsSchool of Nursing, Faculty of Health, Queensland University of Technology, Brisbane, QLD, Australia.
Chris JacobsGraduate School of Health, University of Technology Sydney, Ultimo, NSW, Australia.ORCID 0000-0002-9557-9080
University of Technology Sydney · AUNew South Wales Department of Health · AUQueensland University of Technology · AUThe University of Notre Dame Australia · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Genetic counselling and testing have utility for people with palliative care needs and their families. However, genetic and palliative care health professionals have described difficulties initiating palliative-genetic discussions. Between March and July 2022, we received n = 73 surveys (6% response rate) from genetic and palliative care health professionals in Australia and New Zealand that assessed and compared barriers and facilitators. The main perceived barrier to both groups was palliative care health professionals' lack of genetic knowledge (44%). Most palliative care health professionals were 'not at all confident' performing several activities, including discussing DNA banking (52%) and knowing their legal responsibilities when sharing genetic information (58%). The most frequently selected facilitator for genetic health professionals was fostering close relationships with palliative care health professionals (52%), while palliative care health professionals indicated a genetic referral template (51%) would be of assistance. Almost all participants agreed genetic discussions do not undermine the central ethos of palliative care (87%). Fewer palliative care health professionals considered themselves well situated to have genetic discussions with a palliative patient's family compared to genetic health professionals (p = 0.014). Our results suggest that genetic and palliative care health professionals support integrating genetics into palliative care, although refinement of the palliative care health professionals' role in this process is required. We have identified intervention targets to overcome barriers related to knowledge and confidence, which ought to be integrated into future interventions designed to support health professionals deliver the benefits of genetic information to people with palliative care needs and their families.

Indexed as

Health PersonnelPalliative CareAttitude of Health PersonnelAustraliaHumansQualitative Research

Identifiers

PMID37344570
PMCPMC10772073
OpenAlexW4381597710

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.