Evidence map›Paper›PMID 19265722›Full record

ArticleGenetics in medicine : official journal of the American College of Medical Genetics2009

Factors influencing parental decision about genetics evaluation for their deaf or hard-of-hearing child.

Christina G S Palmer, Jason T Lueddeke, Jin Zhou

Abstract read
In one paragraph

Article in Genetics in medicine : official journal of the American College of Medical Genetics, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed, 2 pooled it
–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

16 citing papers in PubMed, 2 syntheses or guidelines pooled it.

  1. Pooled it
  2. Genetic counseling and testing for Asian Americans: a systematic review.Genetics in medicine : official journal of the American College of Medical Genetics · 2021
    Pooled it
  3. Article
  4. Article
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  6. Review
  7. Prevalence ofExperimental and therapeutic medicine · 2021
    Article
  8. Article
  9. Article
  10. A proposal for comprehensive newborn hearing screening to improve identification of deaf and hard-of-hearing children.Genetics in medicine : official journal of the American College of Medical Genetics · 2019
    Article
  11. Public awareness of ear health and hearing loss in Jeddah, Saudi Arabia.The South African journal of communication disorders = Die Suid-Afrikaanse tydskrif vir Kommunikasieafwykings · 2019
    Article
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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

3 authors.

Christina G S PalmerDepartment of Psychiatry and Biobehavioral Sciences, University of California, Los Angeles, California, USA. cpalmer@mednet.ucla.edu
Jason T Lueddeke
Jin Zhou

Funding

Outcomes of Cx26 Testing in Deaf/Hard of Hearing AdultsR01HG003871 · NHGRI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI PALMER, CHRISTINA GERMAINE · 2006 to 2009
$2.1M
Connexin 26 Testing in InfantsR01DC005663 · NIDCD · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI PALMER, CHRISTINA GERMAINE · 2002 to 2005
$1.4M
NHGRI NIH HHS R01 HG003871NIDCD NIH HHS R01 DC0055663NIDCD NIH HHS R01 DC005663
6 · The paper itself

Abstract

purposeTo identify factors that are associated with why parents of deaf children who have had GJB2/GJB6 testing as part of a genetics research study do or do not take their children for genetics evaluation.

methodsSelf-administered questionnaire was completed by parents of a deaf child participating in a GJB2/GJB6 testing study.

resultsA total of 30 parents (representing 24 children) completed the questionnaire; 11 of 24 children (46%) underwent a genetics evaluation. Compared with parents who did not take their child for a genetics evaluation, those who did were more likely to (1) have supportive pediatricians, (2) feel it was important or would be helpful to their child, (3) recall the recommendation for evaluation, (4) have family members who wanted the child to have an evaluation, and (5) be Hispanic or Asian. Genetic test results, knowledge of genetics evaluation, psychosocial factors, language concerns, or structural factors were not substantively associated with attending a genetics evaluation.

conclusionParental perceptions, family environment, and pediatricians play a role in decisions regarding genetics evaluation. Because genetic testing for deafness likely will occur outside of traditional genetics clinics and without comprehensive genetics evaluation, efforts to increase pediatricians' awareness of the usefulness of genetics evaluation may be essential to ensure appropriate care for deaf and hard-of-hearing children as recommended by the American College of Medical Genetics.

Indexed as

Surveys and QuestionnairesAttitude to HealthChild, PreschoolConnexin 26Connexin 30ConnexinsDeafnessDecision MakingFather-Child RelationsFemaleGenetic Predisposition to DiseaseGenetic TestingHearing LossHumansMaleParentsConnexin 26Connexin 30ConnexinsGJB2 protein, humanGJB6 protein, human

Identifiers

PMID19265722
PMCPMC2822638

What OpenQuestion holds

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LicenceTDM
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.