Literature DB >> 17542006

Assessing parental attitudes toward genetic testing for childhood hearing loss: before and after genetic consultation.

Yuelin Li1, Annie G Steinberg, Lisa Bain, Dinah Yaeger, Ari Bieler, Rachel Ewing, Girija Kaimal, Ian Krantz.   

Abstract

We report on the development of a Genetic Attitude Assessment Tool (GAAT) to measure parental attitudes in contemplating genetic testing for childhood hearing loss, and to examine the differences in assessments made before and after genetic counseling. The GAAT tool was administered to a convenient sample of 119 parents of children with bilateral sensorineural hearing loss. The respondents completed the survey either before (n = 77) or after (n = 42) genetic counseling. Exploratory Factor Analysis was applied to identify and quantify the underlying psychosocial structure. Our results showed the validated 54-item GAAT instrument contains six subscales: (1) "test intention," (2) "beliefs in non-genetic causes of hearing loss," (3) "deferral of decision to undergo genetic testing," (4) "appropriate use of genetic testing results," (5) "beliefs in the benefits," and (6) "concerns about stigma." The respondents who answered the survey after genetic counseling had higher "test intention" (P = 0.017) and endorsed to a greater extent "beliefs in the benefits" (P < 0.001). They believed to a lesser extent that childhood hearing loss was due to "non-genetic causes" (P < 0.001) and were less inclined to prefer "decision deferral" (P = 0.031). Respondents who themselves had a hearing loss expressed a significantly weaker belief in "non-genetic causes" of hearing loss (P < 0.0001). In conclusion the validated GAAT instrument is responsive to changes in parental attitudes after genetic counseling. The GAAT may be used to monitor parental attitudes serially, to further understand how parental attitudes change from pre genetic counseling, post genetic counseling, to post test result disclosure. (c) 2007 Wiley-Liss, Inc

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Year:  2007        PMID: 17542006     DOI: 10.1002/ajmg.a.31730

Source DB:  PubMed          Journal:  Am J Med Genet A        ISSN: 1552-4825            Impact factor:   2.802


  6 in total

1.  Genetic testing and counseling for hereditary neurological diseases in Mali.

Authors:  Katherine Gloria Meilleur; Souleymane Coulibaly; Moussa Traoré; Guida Landouré; Alison La Pean; Modibo Sangaré; Fanny Mochel; Siona Traoré; Kenneth H Fischbeck; Hae-Ra Han
Journal:  J Community Genet       Date:  2011-02-22

2.  Opinions of hearing parents about the causes of hearing impairment of their children with biallelic GJB2 mutations.

Authors:  Aisen V Solovyev; Lilya U Dzhemileva; Olga L Posukh; Nikolay A Barashkov; Marita S Bady-Khoo; Semen L Lobov; Natalya Yu Popova; Georgii P Romanov; Nikolay N Sazonov; Alexander A Bondar; Igor V Morozov; Mikhail I Tomsky; Sardana A Fedorova; Elza K Khusnutdinova
Journal:  J Community Genet       Date:  2017-03-21

Review 3.  Ethical and social implications of genetic testing for communication disorders.

Authors:  Kathleen S Arnos
Journal:  J Commun Disord       Date:  2008-03-25       Impact factor: 2.288

4.  A prospective, longitudinal study of the impact of GJB2/GJB6 genetic testing on the beliefs and attitudes of parents of deaf and hard-of-hearing infants.

Authors:  Christina G S Palmer; Ariadna Martinez; Michelle Fox; Jin Zhou; Nina Shapiro; Yvonne Sininger; Wayne W Grody; Lisa A Schimmenti
Journal:  Am J Med Genet A       Date:  2009-06       Impact factor: 2.802

5.  Non-syndromic sensorineural prelingual deafness: the importance of genetic counseling in demystifying parents' beliefs about the cause of their children's deafness.

Authors:  Fidjy Rodrigues; Milena Paneque; Cláudia Reis; Margarida Venâncio; Jorge Sequeiros; Jorge Saraiva
Journal:  J Genet Couns       Date:  2013-01-26       Impact factor: 2.537

6.  Willingness of women to participate in obstetrical and pediatric research involving biobanks.

Authors:  Renate D Savich; Beth B Tigges; Lisbeth Iglesias Rios; Joanne McCloskey; Kristine Tollestrup; Robert D Annett
Journal:  J Community Genet       Date:  2019-11-28
  6 in total

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