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1.
Hum Reprod ; 35(12): 2643-2649, 2020 12 01.
Artículo en Inglés | MEDLINE | ID: mdl-33326998

RESUMEN

Uterus Transplantation (UTx) is an experimental vascular composite allograft designed to provide women with absolute uterine factor infertility with the opportunity to gestate and give birth to their future offspring. The number of UTx procedures performed worldwide now stands at ≥70 and as the number of cases performed increases so too does the volume of potential data that may be gathered to inform the development, practice and regulation of UTx. Given the value of this data, and the challenges associated with keeping track of cases and outcomes where data remains unpublished and/or scattered, scientists and academics conducting research into UTx have increasingly called for the swift creation, implementation and management of an international registry for Uterus Transplantation (IRUTx). This article explores and provides practical guidance regarding the potential benefits the IRUTx may provide to stakeholders, as well as the legal and ethical challenges that its creation may pose in terms of dataset design, consent, privacy, researcher compliance and governance.


Asunto(s)
Infertilidad Femenina , Trasplante de Órganos , Femenino , Humanos , Sistema de Registros , Trasplante Homólogo , Útero
2.
Med Law Rev ; 23(4): 588-619, 2015.
Artículo en Inglés | MEDLINE | ID: mdl-26232721

RESUMEN

The Report of the Committee of Inquiry into Human Fertilisation and Embryology, the Warnock Report, forms the basis of the UK legislation on embryo research, and its influence continues to be felt, even though over 30 years have passed since its publication. The Warnock Committee was the first of its kind to consider how advancements in human fertilisation and embryology should be regulated. This article examines the evidence submitted to the Warnock Committee, upon which its members ultimately reached their conclusions. With ongoing debate as to the status of the human embryo, it is important to recognise that the legislative position is one that was reached after extensive consultation and consideration of submitted evidence by the Warnock Committee. This article considers the differing ethical viewpoints that were expressed by organisations both prior and post-publication of the Warnock Report, and how the Committee used that evidence to reach their conclusions, and ultimately calls for a new Warnock-style committee.


Asunto(s)
Comienzo de la Vida Humana/ética , Investigaciones con Embriones/legislación & jurisprudencia , Evaluación de la Tecnología Biomédica/legislación & jurisprudencia , Comités Consultivos , Bioética , Investigaciones con Embriones/ética , Regulación Gubernamental , Humanos , Consentimiento Informado/ética , Personeidad , Religión y Medicina , Evaluación de la Tecnología Biomédica/ética , Evaluación de la Tecnología Biomédica/métodos , Reino Unido
4.
J Bioeth Inq ; 14(4): 461-468, 2017 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-29110172

RESUMEN

This discussion follows a series of high profile cases involving a terminally ill child, Charlie Gard. These cases are significant as they trace the complexities that arise when parents and medical teams do not agree as well as addressing the question of whether there is a right to access experimental treatment.


Asunto(s)
Toma de Decisiones/ética , Accesibilidad a los Servicios de Salud/ética , Derechos Humanos , Padres , Médicos/ética , Enfermo Terminal , Terapias en Investigación , Niño , Ética Médica , Accesibilidad a los Servicios de Salud/legislación & jurisprudencia , Humanos , Participación del Paciente , Médicos/legislación & jurisprudencia , Relaciones Profesional-Familia , Enfermo Terminal/legislación & jurisprudencia , Privación de Tratamiento/ética , Privación de Tratamiento/legislación & jurisprudencia
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