Evidence map›Paper›PMID 39822264›Full record

ArticleGenetics in medicine open2024

Frequency and reasons that parents decline genetic testing for critically ill neonates.

Katharine Press Callahan, Rebecca Mueller, Karen Crew, Kyle Brothers, David Munson, Steven Joffe, Chris Feudtner

Abstract read
In one paragraph

Article in Genetics in medicine open, 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
–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

2 citing papers in PubMed.

  1. Article
  2. Parents' perceptions of the utility of genetic testing in the NICU.Genetics in medicine : official journal of the American College of Medical Genetics · 2025
    Article
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.

Katharine Press CallahanThe Children's Hospital of Philadelphia, Philadelphia, PA.
Rebecca MuellerDepartment of Medical Ethics and Health Policy, The Perelman School of Medicine at the University of Pennsylvania, Philadelphia, PA.
Karen CrewThe Children's Hospital of Philadelphia, Philadelphia, PA.
Kyle BrothersNorton Children's Research Institute Affiliated with the University of Louisville School of Medicine, Louisville, KY.
David MunsonThe Children's Hospital of Philadelphia, Philadelphia, PA.
Steven JoffeThe Children's Hospital of Philadelphia, Philadelphia, PA.
Chris FeudtnerThe Children's Hospital of Philadelphia, Philadelphia, PA.

Funding

The Penn Postdoctoral Training Program in the Ethical, Legal and Social Implications of Genetics and GenomicsT32HG009496 · NHGRI · UNIVERSITY OF PENNSYLVANIA · PI Steven Joffe · 2017 to 2026
$3.4M
Managing the Uncertainty of Genetic Information in NeonatesK01HG013114 · NHGRI · CHILDREN'S HOSP OF PHILADELPHIA · PI Katharine Press Callahan · 2023 to 2026
$664k
NHGRI NIH HHS K01 HG013114NHGRI NIH HHS T32 HG009496
6 · The paper itself

Abstract

Purpose: Current literature reports strong support among parents for genetic testing for ill neonates; yet, some parents decline this testing for unknown reasons. We aimed to document the proportion of parents who decline, describe their clinical and demographic characteristics, and categorize their rationales. Methods: We reviewed medical records to collect and compare clinical and demographic information for patients whose parents consented to and declined recommended genetic testing. We also conducted brief interviews with parents who declined testing to discover their rationales. Results: Fifty-one of 247 parents (21%) declined recommended genetic testing. The most common reason for declining, cited by 83% of parents interviewed, was that the testing felt irrelevant to the problems they saw as most important. The second most common reason, cited by 63%, was worrying that the testing might yield unwanted information. Compared with parents who consented, those who declined were more likely to be making the decision for a child with a prenatally diagnosed condition ( Conclusion: Parents who decline genetic testing for ill neonates provide an alternate appraisal of benefits and harms which should be incorporated into informing future parents considering these tests.

Indexed as

BioethicsCritical careEthicsGeneticsNeonatology

Identifiers

PMID39822264
PMCPMC11736172

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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.