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1.
J Bioeth Inq ; 14(1): 109-121, 2017 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-27761875

RESUMO

New-born screening programs for congenital disorders and chronic disease are expanding worldwide and children "at risk" are identified by nationwide tracking systems at the earliest possible stage. These practices are never neutral and raise important social and ethical questions. An emergent concern is that a reflexive professionalism should interrogate the ever earlier interference in children's lives. The Flemish community of Belgium was among the first to generalize the screening for hearing loss in young children and is an interesting case to study the public justification of early interventions for families with deaf children. This article uses a critical lens to study the archive of the government child healthcare organization in Flanders in order to uncover underlying constructions of childhood, deafness, and preventive health. We focus on two interrelated themes. The first is the notion of exclusion of the human factor through the mediation of technology. The second is the idea of deafness as endangering a healthy development, an impairment that can nevertheless be treated if detected early enough. It is argued that, since deafness cannot be viewed as a life-threatening condition, the public interest which is implicitly defended is not the rescue of deaf children rather the exclusion of otherness.


Assuntos
Correção de Deficiência Auditiva/ética , Surdez/diagnóstico , Intervenção Educacional Precoce/ética , Triagem Neonatal/ética , Fatores Etários , Bélgica , Surdez/congênito , Surdez/terapia , Diagnóstico Precoce , Humanos , Recém-Nascido , Programas de Rastreamento/ética , Avaliação de Programas e Projetos de Saúde
2.
Am Ann Deaf ; 155(3): 339-52, 2010.
Artigo em Inglês | MEDLINE | ID: mdl-21138046

RESUMO

Factors contributing to parents' decision when they choose between cochlear implantation (CI) and traditional hearing aids for their child were examined. The subjects were children with severe/profound hearing loss, born 1999-2001, registered in the universal neonatal hearing screening program in the Flanders region of Belgium. Qualitative data collected retrospectively from parents were subjected to thematic content analysis. In their responses to professional advice, parents were segmented into 3 groups: (a) those whose primary considerations were the importance of oral language development and the relative potential of CI and traditional hearing aids; (b) those for whom alternative factors (e.g., medical risks, ethical issues) were paramount, even in the face of professional advocacy of CI; (c) those who followed professional advice against CI. The researchers conclude that care professionals should be sensitive to the impact of their advice and other factors in parental decision making.


Assuntos
Implante Coclear/instrumentação , Implantes Cocleares , Correção de Deficiência Auditiva/psicologia , Tomada de Decisões , Auxiliares de Audição , Pais/psicologia , Pessoas com Deficiência Auditiva/psicologia , Pessoas com Deficiência Auditiva/reabilitação , Atitude do Pessoal de Saúde , Bélgica , Criança , Pré-Escolar , Comportamento de Escolha , Implante Coclear/efeitos adversos , Implante Coclear/psicologia , Feminino , Conhecimentos, Atitudes e Prática em Saúde , Humanos , Masculino , Relações Profissional-Família , Pesquisa Qualitativa , Estudos Retrospectivos , Medição de Risco , Inquéritos e Questionários
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