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1.
Disabil Health J ; 16(2): 101401, 2023 04.
Artigo em Inglês | MEDLINE | ID: mdl-36463093

RESUMO

While prenatal screening and testing have expanded substantially over the past decade and provide access to more genetic information, expectant parents are more likely to describe the diagnosis experience as negative than positive. In addition, the conversations that take place during these experiences sometimes reflect unconscious bias against people with disabilities. Consequently, an interdisciplinary committee of experts, including people with disabilities, family members, disability organization leaders, healthcare and genetics professionals, and bioethicists, reviewed selected published and gray literature comparing the current state of the administration of prenatal testing to the ideal state. Subsequently, the interdisciplinary team created recommendations for clinicians, public health agencies, medical organizations, federal agencies, and other stakeholders involved with administering prenatal screening and testing to create better patient experiences; conduct training for healthcare professionals; create, enforce, and fund policies and guidelines; and engage in more robust data collection and research efforts.


Assuntos
Pessoas com Deficiência , Gravidez , Feminino , Humanos , Diagnóstico Pré-Natal , Pessoal de Saúde , Saúde Pública , Avaliação de Resultados da Assistência ao Paciente
2.
Intellect Dev Disabil ; 54(2): 84-93, 2016 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-27028250

RESUMO

Since the dawn of prenatal testing in the 1970s, concerns have been raised over its administration to respect a mother's autonomy as well as the expressive critique against those with the tested-for condition. Advances in prenatal testing have made it such that more mothers than ever are given a test result of Down syndrome, yet are not provided the rest of the information recommended by professional guidelines. In response, first federal legislation and then, increasingly, state legislation is requiring that this information be provided to expectant mothers. Though receiving broad bipartisan support in passage, some of the statutes have received criticism. These public policy measures will be surveyed and evaluated as to their relative merits and limitations.


Assuntos
Síndrome de Down/diagnóstico , Síndrome de Down/genética , Aconselhamento Genético/ética , Diagnóstico Pré-Natal/ética , Política Pública , Feminino , Aconselhamento Genético/legislação & jurisprudência , Humanos , Autonomia Pessoal , Gravidez , Diagnóstico Pré-Natal/métodos , Política Pública/legislação & jurisprudência , Estados Unidos
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