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Patients' choices and opinions on chorionic villous sampling and non-invasive alternatives for prenatal testing following preimplantation genetic testing for hereditary disorders: A cross-sectional questionnaire study.
Toft, Christian L F; Diemer, Tue; Ingerslev, Hans J; Pedersen, Inge S; Adrian, Stine W; Kesmodel, Ulrik S.
Afiliación
  • Toft CLF; Department of Molecular Diagnostics, Aalborg University Hospital, Aalborg, Denmark.
  • Diemer T; Center for Preimplantation Genetic Testing, Aalborg University Hospital, Aalborg, Denmark.
  • Ingerslev HJ; Department of Clinical Medicine, Aalborg University, Aalborg, Denmark.
  • Pedersen IS; Center for Preimplantation Genetic Testing, Aalborg University Hospital, Aalborg, Denmark.
  • Adrian SW; Department of Clinical Genetics, Aalborg University Hospital, Aalborg, Denmark.
  • Kesmodel US; Center for Preimplantation Genetic Testing, Aalborg University Hospital, Aalborg, Denmark.
Prenat Diagn ; 42(2): 212-225, 2022 Feb.
Article en En | MEDLINE | ID: mdl-34997771
ABSTRACT

OBJECTIVE:

The aim of this study was to investigate choices of and reasoning behind chorionic villous sampling and opinions on non-invasive prenatal testing among women and men achieving pregnancy following preimplantation genetic testing (PGT) for hereditary disorders.

METHODS:

A questionnaire was electronically submitted to patients who had achieved a clinical pregnancy following PGT at the Center for Preimplantation Genetic Testing, Aalborg University Hospital, Denmark, between 2017 and 2020.

RESULTS:

Chorionic villous sampling was declined by approximately half of the patients. The primary reason for declining was the perceived risk of miscarriage due to the procedure. Nine out of 10 patients responded that they would have opted for a non-invasive prenatal test if it had been offered. Some patients were not aware that the nuchal translucency scan offered to all pregnant women in the early second trimester only rarely provides information on the hereditary disorder for which PGT was performed.

CONCLUSION:

Improved counseling on the array of prenatal tests and screenings available might be required to assist patients in making better informed decisions regarding prenatal testing. Non-invasive prenatal testing is welcomed by the patients and will likely increase the number of patients opting for confirmatory prenatal testing following PGT for hereditary disorders.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Muestra de la Vellosidad Coriónica / Aceptación de la Atención de Salud / Pruebas Genéticas / Diagnóstico Preimplantación / Prioridad del Paciente / Pruebas Prenatales no Invasivas / Enfermedades Genéticas Congénitas Tipo de estudio: Diagnostic_studies / Observational_studies / Prevalence_studies / Prognostic_studies / Qualitative_research / Risk_factors_studies Límite: Adult / Female / Humans / Male / Pregnancy Idioma: En Revista: Prenat Diagn Año: 2022 Tipo del documento: Article País de afiliación: Dinamarca

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Muestra de la Vellosidad Coriónica / Aceptación de la Atención de Salud / Pruebas Genéticas / Diagnóstico Preimplantación / Prioridad del Paciente / Pruebas Prenatales no Invasivas / Enfermedades Genéticas Congénitas Tipo de estudio: Diagnostic_studies / Observational_studies / Prevalence_studies / Prognostic_studies / Qualitative_research / Risk_factors_studies Límite: Adult / Female / Humans / Male / Pregnancy Idioma: En Revista: Prenat Diagn Año: 2022 Tipo del documento: Article País de afiliación: Dinamarca