Evidence map›Paper›PMID 41251905›Full record

ArticleJournal of community genetics2025

Universal newborn screening for familial hypercholesterolaemia-insights from healthcare professionals in Queensland, Australia.

Caroline Bachmeier, Deborah Johnston, Karam Kostner, Andrew Kassianos

Abstract read
In one paragraph

Article in Journal of community genetics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

4 authors.

Caroline BachmeierUniversity of Queensland, Brisbane, QLD, Australia. c.bachmeier@uq.edu.au.ORCID http://orcid.org/0000-0003-0510-7264
Deborah JohnstonSchool of Population Health, Faculty of Medicine and Health, University of New South Wales, Sydney, NSW, Australia.
Karam KostnerUniversity of Queensland, Brisbane, QLD, Australia.
Andrew KassianosKidney Health Service, Royal Brisbane and Women's Hospital, Brisbane, QLD, Australia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background Familial hypercholesterolaemia is a common disorder leading to premature atherosclerotic cardiovascular disease. Despite available treatment options and guideline recommendations for early screening and intervention, fewer than 10% (1 in 10) of individuals with familial hypercholesterolaemia have been identified. Objective To assess if healthcare providers in Queensland, Australia, support introduction of newborn screening for familial hypercholesterolaemia with a focus on benefits, concerns, barriers, and solutions. Methods A survey consisting of 16 items was conducted. Healthcare providers in Endocrinology, Cardiology, Chemical Pathology, Genetic Pathology, Clinical Genetics, General Practice and Genetic Counselling were invited to participate. Results 69 individuals completed the survey. There was strong support for newborn screening for familial hypercholesterolaemia including via genetic testing. Perceived benefits of genetic testing included early diagnosis, prevention of heart disease, reverse cascade screening, robust screening methodology and family planning. Concerns included access to insurance, technical understanding of genetics, parental anxiety, burden to the healthcare system, genetic discrimination, non-paternity, impact on the psychological health of children, child-parent bonding, and delay from diagnosis to initiation of pharmacotherapy during childhood. Main perceived barriers were cost and burden to the healthcare system, lack of a formal consent process and follow-up pathways. A multidisciplinary approach with appropriate funding, education, a formalized consent process and follow-up pathways with local pilot testing were perceived as important steps to overcome these barriers. Conclusion There was widespread support for newborn screening for familial hypercholesterolaemia in a diverse group of healthcare professionals. Further work is required to address concerns and barriers prior to introduction of newborn screening for familial hypercholesterolaemia.

Identifiers

PMID41251905
PMCPMC12627328

What OpenQuestion holds

Textmetadata
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.