Evidence map›Paper›PMID 40175825›Full record

ArticleJournal of community genetics2025

Experience of people with Biochemical Genetic Disorders and their families accessing Genetic Counselling and Genetic Testing in the Irish Republic.

Arnott C, Ward Aj, Lambert Dm, Butterly D, McGrath V, Lynch Sa, O 'Byrne Jj

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

7 authors.

Arnott CSchool of Medicine, University College Dublin, Dublin, Ireland.
Ward AjSchool of Medicine, University College Dublin, Dublin, Ireland. alanaward@btinternet.com.ORCID http://orcid.org/0009-0003-6486-0421
Lambert DmSchool of Medicine, University College Dublin, Dublin, Ireland.ORCID http://orcid.org/0000-0003-0967-0476
Butterly DSchool of Medicine, University College Dublin, Dublin, Ireland.
McGrath VRare Diseases Ireland, Dublin, Ireland.
Lynch SaSchool of Medicine, University College Dublin, Dublin, Ireland.ORCID http://orcid.org/0000-0003-3540-1333
O 'Byrne JjSchool of Medicine, University College Dublin, Dublin, Ireland.ORCID http://orcid.org/0000-0003-3162-2411

Funding

Adelaide Health Foundation R22808Irish Society of Human Genetics 2024 Summer Research Studentship
6 · The paper itself

Abstract

backgroundNational and international reports recommend that genetic counselling should be made available to parents of children living with inherited rare diseases; and to patients themselves upon turning 16-18 years old. Long wait times of up to two years for genetic counselling through Children's Health Ireland contributed to a lack of accessibility for adult patients with inherited metabolic disorders (IMDs). At the time of the study, the National Centre for Inherited Metabolic Disorders (NCIMD) Mater, which takes care of ~ 1400 adult patients with genetic disorders primarily affecting biochemical pathways, did not have direct access to a genetic counsellor. OBJECTIVES AND

methodsAn online survey was conducted to investigate the genetic testing and counselling experiences of adult patients with rare IMDs and their families within the Republic of Ireland.

resultsThe NCIMD-Mater survey highlighted a lack of patient knowledge of and access to genetic counselling services; with some patients unaware of and others incorrectly understanding the role of genetic counselling. Most patients who underwent genetic testing were tested by a non-genetic healthcare professional. Satisfaction levels of genetic counselling services were mixed with some patients reporting delaying personal life and family plans due to wait times for genetic counselling.

conclusionThis study highlights deficiencies in the genetic testing and counselling experience of Irish IMD patients. Embedding genetic counselling into multidisciplinary IMD teams would increase access to genetics education for patients and families and improve the clinical service. This study may be utilized to measure the impact of integrating genetic counsellors into NCIMD-Mater.

Indexed as

BackgroundGenetic counsellingGenetic testingPatient experienceRare metabolic disease

Identifiers

PMID40175825
PMCPMC12401831

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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.