Evidence map›Paper›PMID 42362800›Full record

ArticleEuropean journal of human genetics : EJHG2026

How parents decide whether to have genomic newborn screening: experiences from BabyScreen.

Anaita Kanga-Parabia, Erin Tutty, Nathasha Kugenthiran, Jade Caruana, Lilian Downie, Clara Gaff, Nitzan Lang, Sebastian Lunke, Katrina Scarff, Zornitza Stark and 2 more

Abstract read
PubMed Publisher
In one paragraph

Article in European journal of human genetics : EJHG, 2026. 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

12 authors.

Anaita Kanga-ParabiaUniversity of Melbourne, Melbourne, VIC, Australia.ORCID http://orcid.org/0000-0003-4656-9246
Erin TuttyUniversity of Melbourne, Melbourne, VIC, Australia.
Nathasha KugenthiranUniversity of Melbourne, Melbourne, VIC, Australia.ORCID http://orcid.org/0009-0003-3575-4347
Jade CaruanaMurdoch Children's Research Institute, Parkville, VIC, Australia.ORCID http://orcid.org/0000-0003-0335-6224
Lilian DownieUniversity of Melbourne, Melbourne, VIC, Australia.ORCID http://orcid.org/0000-0003-3914-5592
Clara GaffUniversity of Melbourne, Melbourne, VIC, Australia.
Nitzan LangVictorian Clinical Genetics Services, Murdoch Children's Research Institute, Parkville, VIC, Australia.
Sebastian LunkeUniversity of Melbourne, Melbourne, VIC, Australia.ORCID http://orcid.org/0000-0002-7168-0723
Katrina ScarffVictorian Clinical Genetics Services, Murdoch Children's Research Institute, Parkville, VIC, Australia.ORCID http://orcid.org/0000-0002-5195-9727
Zornitza StarkUniversity of Melbourne, Melbourne, VIC, Australia.
Stephanie BestUniversity of Melbourne, Melbourne, VIC, Australia. Stephanie.best@unimelb.edu.au.ORCID http://orcid.org/0000-0002-1107-8976
Alison D ArchibaldUniversity of Melbourne, Melbourne, VIC, Australia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Education and consent processes for genomic newborn screening (gNBS) must be informed by evidence about parental decision-making. BabyScreen+ piloted gNBS for 1000 newborns in Victoria, Australia. Prospective parents consented online with genetic counselling available on request. We aimed to explore how BabyScreen+ participants (n = 1139) made decisions about gNBS using a convergent parallel mixed methods design. Demographic (n = 1080), survey (n = 1010), and interview (n = 24) data were analysed using descriptive statistics, logistic regression, and deductive content analysis mapped to the Health Belief Model (domains indicated in italics). Most participants perceived low susceptibility of having a child with a genetic condition and found it difficult to conceptualise severity. Participants were motivated to consider gNBS due to benefits such as information about their child's health, reassurance, and research contributions. Some perceived barriers included inequitable access to gNBS information, difficulty navigating high chance results, and potential data misuse. Most participants (987/1139, 87%) proceeded with gNBS because they believed barriers were outweighed by benefits or were manageable due to high self-efficacy. Remaining participants (152/1139, 13%) did not proceed with gNBS because benefits were unclear, or due to low self-efficacy. Experiences were modified by sociodemographic factors and the BabyScreen+ model of care. This research provides timely evidence about parental gNBS decision-making. It supports acceptability and feasibility of the BabyScreen+ model of care. Moving forward, education and consent processes must be equitable, tailored to individual context, and designed to foster self-efficacy. Such considerations will support decision-making and reduce psychological impacts for parents considering gNBS in the future.

Identifiers

PMID42362800

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.