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Impact of prenatal exome sequencing for fetal genetic diagnosis on maternal psychological outcomes and decisional conflict in a prospective cohort.
Talati, Asha N; Gilmore, Kelly L; Hardisty, Emily E; Lyerly, Anne D; Rini, Christine; Vora, Neeta L.
Afiliação
  • Talati AN; Department of Obstetrics and Gynecology, Division of Maternal-Fetal Medicine University of North Carolina School of Medicine, Chapel Hill, NC, USA. asha_talati@med.unc.edu.
  • Gilmore KL; Department of Obstetrics and Gynecology, Division of Maternal-Fetal Medicine University of North Carolina School of Medicine, Chapel Hill, NC, USA.
  • Hardisty EE; Department of Obstetrics and Gynecology, Division of Maternal-Fetal Medicine University of North Carolina School of Medicine, Chapel Hill, NC, USA.
  • Lyerly AD; Department of Social Medicine and Center for Bioethics, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.
  • Rini C; Department of Medical Social Sciences, Northwestern University Feinberg School of Medicine and the Robert H. Lurie Comprehensive Cancer Center of Northwestern University, Chicago, IL, USA.
  • Vora NL; Department of Obstetrics and Gynecology, Division of Maternal-Fetal Medicine University of North Carolina School of Medicine, Chapel Hill, NC, USA.
Genet Med ; 23(4): 713-719, 2021 04.
Article em En | MEDLINE | ID: mdl-33214710
ABSTRACT

PURPOSE:

To evaluate associations between prenatal trio exome sequencing (trio-ES) and psychological outcomes among women with an anomalous pregnancy.

METHODS:

Trio-ES study enrolling patients with major fetal anomaly and normal microarray. Women completed self-reported measures and free response interviews at two timepoints pre- (1) and post- (2) sequencing. Pre-sequencing responses were compared with post-sequencing responses; post-sequencing responses were stratified by women who received trio-ES results that may explain fetal findings, secondary findings (medically actionable or couples with heterozygous variants for the same recessive disorder), or negative results.

RESULTS:

One hundred fifteen trios were enrolled. Of those, 41/115 (35.7%) received results from trio-ES, including 36 (31.3%) who received results that may explain the fetal phenotype. These women had greater post-sequencing distress compared with women who received negative results, including generalized distress (p = 0.03) and test-related distress (p = 0.2); they also had worse psychological adaptation to results (p = 0.001). Genomic knowledge did not change from pre- to post-sequencing (p = 0.51).

CONCLUSION:

Women show more distress after receiving trio-ES results compared with those who do not, suggesting that women receiving results may need additional support or counseling to inform current and future reproductive decisions.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Ultrassonografia Pré-Natal / Exoma Tipo de estudo: Diagnostic_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Female / Humans / Pregnancy Idioma: En Revista: Genet Med Assunto da revista: GENETICA MEDICA Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Ultrassonografia Pré-Natal / Exoma Tipo de estudo: Diagnostic_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Female / Humans / Pregnancy Idioma: En Revista: Genet Med Assunto da revista: GENETICA MEDICA Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Estados Unidos