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1.
J Bioeth Inq ; 21(1): 193-208, 2024 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-38532187

RESUMO

This study's objective was to understand Colombian adolescents' experiences and preferences regarding access to sexual and reproductive health services (SRHS), either alone or accompanied. A mixed-method approach was used, involving a survey of 812 participants aged eleven to twenty-four years old and forty-five semi-structured interviews with participants aged fourteen to twenty-three. Previous research shows that adolescents prefer privacy when accessing SRHS and often do not want their parents involved. Such findings align with the longstanding tendency to frame the ethical principle of autonomy as based on independence in decision-making. However, the present study shows that such a conceptualization and application of autonomy does not adequately explain Colombian adolescent participants' preferences regarding access to SRHS. Participants shared a variety of preferences to access SRHS, with the majority of participants attaching great importance to having their parents involved, to varying degrees. What emerges is a more complex and non-homogenous conceptualization of autonomy that is not inherently grounded in independence from parental involvement in access to care. We thus argue that when developing policies involving adolescents, policymakers and health professionals should adopt a nuanced "relational autonomy" approach to better respect the myriad of preferences that Colombian (and other) adolescents may have regarding their access to SRHS.


Assuntos
Acessibilidade aos Serviços de Saúde , Autonomia Pessoal , Serviços de Saúde Reprodutiva , Humanos , Adolescente , Colômbia , Serviços de Saúde Reprodutiva/ética , Acessibilidade aos Serviços de Saúde/ética , Feminino , Masculino , Adulto Jovem , Criança , Tomada de Decisões , Pais/psicologia , Saúde Sexual , Comportamento Sexual , Privacidade
2.
J Dev Orig Health Dis ; 8(4): 436-442, 2017 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-28535841

RESUMO

The use of assisted reproductive technologies (ART) has increased significantly, allowing many coping with infertility to conceive. However, an emerging body of evidence suggests that ART could carry epigenetic risks for those conceived through the use of these technologies. In accordance with the Developmental Origins of Health and Disease hypothesis, ART could increase the risk of developing late-onset diseases through epigenetic mechanisms, as superovulation, fertilization methods and embryo culture could impair the embryo's epigenetic reprogramming. Such epigenetic risks raise ethical issues for all stakeholders: prospective parents and children, health professionals and society. This paper focuses on ethical issues raised by the consideration of these risks when using ART. We apply two key ethical principles of North American bioethics (respect for autonomy and non-maleficence) and suggest that an ethical tension may emerge from conflicting duties to promote the reproductive autonomy of prospective parents on one hand, and to minimize risks to prospective children on the other. We argue that this tension is inherent to the entire enterprise of ART and thus cannot be addressed by individual clinicians in individual cases. We also consider the implications of the 'non-identity problem' in this context. We call for additional research that would allow a more robust evidence base for policy. We also call upon professional societies to provide clinicians with guidelines and educational resources to facilitate the communication of epigenetic risks associated with ART to patients, taking into consideration the challenges of communicating risk information whose validity is still uncertain.


Assuntos
Epigênese Genética/genética , Pessoal de Saúde/ética , Autonomia Pessoal , Relações Médico-Paciente/ética , Técnicas de Reprodução Assistida/ética , Feminino , Pessoal de Saúde/normas , Humanos , Técnicas de Reprodução Assistida/normas
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