Literature DB >> 33128404

Personalized prenatal genomic testing: Couples' experience with choice regarding uncertain and adult-onset findings from chromosomal-microarray-analysis.

Talya Millo1, Liza Douiev1, Dov Popper1, Shiri Shkedi-Rafid1,2.   

Abstract

BACKGROUND: Chromosomal-microarray-analysis (CMA) can identify variants of uncertain clinical significance, susceptibility-loci for neurodevelopmental conditions, and risk for adult-onset conditions. We explored choices made by couples undergoing prenatal CMA, their understanding of these findings, reasons for and against receiving them, and whether they believe parents or professionals should decide which are disclosed.
METHODS: Semi-structured interviews were conducted with women (n = 27) or their partners (n = 15) during the week following prenatal CMA testing and analyzed using grounded theory.
RESULTS: Over half the interviewees (55%) recalled at least two of the three types of CMA results they chose whether to receive. Sixty-four percent found the choice simple, whereas 36% found it difficult. All participants could clearly explain their choices, which were based on the perceived actionability and psychological impact of the information. Sixty percent viewed their choice favorably, whereas ~21% would have preferred clinicians to decide for them. More women than men, and more decisive than indecisive participants supported parental choice.
CONCLUSION: Overall, expectant parents can make informed choices about which uncertain findings about their fetuses they wish to receive, and value the opportunity to tailor results to their values and wishes. Arguments presented provide the basis for a decision-aid tool for expecting parents.
© 2020 John Wiley & Sons Ltd.

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Year:  2020        PMID: 33128404     DOI: 10.1002/pd.5856

Source DB:  PubMed          Journal:  Prenat Diagn        ISSN: 0197-3851            Impact factor:   3.050


  4 in total

1.  Postpartum women's attitudes to disclosure of adult-onset conditions in pregnancy.

Authors:  Vitalia Libman; Michal Macarov; Yechiel Friedlander; Sidra Goldman-Mellor; Salomon Israel; Drorith Hochner-Celnikier; Yishai Sompolinsky; Uri Pinchas Dior; Michael Osovsky; Lina Basel-Salmon; Arnon Wiznitzer; Yehuda Neumark; Vardiella Meiner; Ayala Frumkin; Shiri Shkedi-Rafid; Hagit Hochner
Journal:  Prenat Diagn       Date:  2022-05-04       Impact factor: 3.242

2.  Views of Israeli healthcare professionals regarding communication of genetic variants of uncertain significance to patients.

Authors:  Alma Levin Fridman; Aviad Raz; Stefan Timmermans; Shiri Shkedi-Rafid
Journal:  J Genet Couns       Date:  2022-02-04       Impact factor: 2.717

3.  Fragmented responsibility: views of Israeli HCPs regarding patient recontact following variant reclassification.

Authors:  Alma Levin Fridman; Aviad Raz; Stefan Timmermans; Shiri Shkedi-Rafid
Journal:  J Community Genet       Date:  2021-10-05

Review 4.  Molecular Approaches in Fetal Malformations, Dynamic Anomalies and Soft Markers: Diagnostic Rates and Challenges-Systematic Review of the Literature and Meta-Analysis.

Authors:  Gioia Mastromoro; Daniele Guadagnolo; Nader Khaleghi Hashemian; Enrica Marchionni; Alice Traversa; Antonio Pizzuti
Journal:  Diagnostics (Basel)       Date:  2022-02-23
  4 in total

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