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Experiences of nonpregnant couples after receiving reproductive genetic carrier screening results in Belgium.
Van Steijvoort, Eva; Peeters, Hilde; Vandecruys, Hilde; Verguts, Jasper; Peeraer, Karen; Matthijs, Gert; Borry, Pascal.
Afiliação
  • Van Steijvoort E; Department of Public Health and Primary Care, KU Leuven, Leuven, Belgium. eva.vansteijvoort@kuleuven.be.
  • Peeters H; Department of Human Genetics, KU Leuven, Leuven, Belgium.
  • Vandecruys H; Department of Gynecology and Obstetrics, Jessa Ziekenhuis Hasselt, Hasselt, Belgium.
  • Verguts J; Department of Gynecology and Obstetrics, Jessa Ziekenhuis Hasselt, Hasselt, Belgium.
  • Peeraer K; Department of Development and Regeneration, KU Leuven, Leuven, Belgium.
  • Matthijs G; Department of Human Genetics, KU Leuven, Leuven, Belgium.
  • Borry P; Department of Public Health and Primary Care, KU Leuven, Leuven, Belgium.
Eur J Hum Genet ; 31(6): 696-702, 2023 06.
Article em En | MEDLINE | ID: mdl-36788144
Reproductive genetic carrier screening (RGCS) allows for the identification of couples who have an increased likelihood of conceiving a child with a particular autosomal recessive or X-linked condition. The aim of this study was to assess the level of satisfaction, anxiety, knowledge retention, psychosocial and counseling-related aspects among couples who chose to have RGCS. Participants were initially informed about their screening results by telephone. After obtaining a written report of test results, participants were asked to complete an individual self-administered questionnaire. All participants (n = 67) felt they had enough information to make an informed choice. None of the participants regretted their choice to have RGCS. Test results were most often shared with parents (61%) or siblings (37%). Our findings demonstrate that the information/counseling and reporting strategy that was used in the context of this study led to high participant satisfaction, an increase in knowledge over time and favorable psychosocial and counseling-related outcomes.
Assuntos

Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Testes Genéticos / Aconselhamento Genético Tipo de estudo: Diagnostic_studies / Prognostic_studies / Screening_studies Limite: Child / Humans País/Região como assunto: Europa Idioma: En Revista: Eur J Hum Genet Assunto da revista: GENETICA MEDICA Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Bélgica

Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Testes Genéticos / Aconselhamento Genético Tipo de estudo: Diagnostic_studies / Prognostic_studies / Screening_studies Limite: Child / Humans País/Região como assunto: Europa Idioma: En Revista: Eur J Hum Genet Assunto da revista: GENETICA MEDICA Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Bélgica