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1.
J Genet Couns ; 27(4): 894-901, 2018 08.
Artigo em Inglês | MEDLINE | ID: mdl-29247311

RESUMO

Recently, practices have begun integrating cell-free DNA-based noninvasive prenatal screening as a screening option for a variety of genetic conditions. According to the National Society of Genetic Counselors, the integration of cfDNA screening into clinical prenatal practice may "significantly shift the paradigm of prenatal testing and screening for all women." The purpose of this study was to determine whether group information sessions can feasibly serve as an alternative to extended one-on-one genetic counseling for the increasing number of women making decisions about prenatal testing and screening. This study assessed the effect of group genetic information sessions coupled with abbreviated counseling on pregnant women's knowledge about and attitudes toward prenatal testing and screening.


Assuntos
Transtornos Cromossômicos/diagnóstico , Aconselhamento Genético/métodos , Testes Genéticos/métodos , Diagnóstico Pré-Natal/métodos , Atitude Frente a Saúde , Transtornos Cromossômicos/psicologia , Tomada de Decisões , Feminino , Aconselhamento Genético/psicologia , Humanos , Gravidez , Diagnóstico Pré-Natal/psicologia
2.
J Womens Health (Larchmt) ; 26(7): 755-761, 2017 07.
Artigo em Inglês | MEDLINE | ID: mdl-28388340

RESUMO

AIMS: In September, 2015, Mayo Clinic convened a panel of national thought leaders on prenatal screening, medical genetics, and obstetrics and gynecology practice. RESULTS: During the 2-day symposium, participants discussed the implications of the shift toward broader prenatal screening using cell-free placental DNA in maternal serum (cfDNA screening). Key topics included challenges around the pace of change in the prenatal screening market, uncertainty around reimbursement, meeting the need for patient counseling, and potential challenges in interpreting and returning cfDNA screening results. INNOVATION: Here, we describe the challenges discussed and offer clinical recommendations for practices who are working to meet them. CONCLUSION: As the spread of prenatal genetic screening continues, providers will increasingly need to update their practice to accommodate new screening modalities.


Assuntos
DNA/sangue , Testes Genéticos/métodos , Genômica , Obstetrícia , Guias de Prática Clínica como Assunto , Diagnóstico Pré-Natal , Feminino , Aconselhamento Genético , Ginecologia , Humanos , Gravidez
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