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dc.contributor.authorAniaka, Oluchukwu Jacinta
dc.date.accessioned2012-08-29T15:13:27Z
dc.date.available2012-08-29T15:13:27Z
dc.date.issued2012-08-29
dc.identifier.urihttp://hdl.handle.net/10222/15420
dc.descriptionThe thesis is the first part of a two part plan for operationalizing patient right in Nigeriaen_US
dc.description.abstractThe notion of informed consent to medical treatment is a fundamental precept in law. It recognizes autonomy and the right to personal inviolability, irrespective of nationality, socio-economic situation and ideological orientation. A full realization of autonomy in the Nigerian legal system is severely constricted by sociological and cultural factors. Of particular concern is the impact of oppression which may arise from socialization, arbitrary disclosure practice by physicians, or as a result of legislative enactment. To remedy the elemental defects in the Nigerian Code of Medical Ethics, without addressing the impediments posed by the social environment from which a patient operates, will nuance informed consent in Nigerian health care but may not fully realize patient autonomy. A serious commitment to respecting patient autonomy may be realized through a collective effort of the State, the medical profession, the community, and patients in order to remove the impediments to full exercise of autonomy.en_US
dc.subjectInformed Consent Nigerian Health Careen_US
dc.titleMaking Informed Consent Work in Nigerian Health Careen_US
dc.typeThesisen_US
dc.date.defence2012-08-14
dc.contributor.departmentFaculty of Lawen_US
dc.contributor.degreeMaster of Lawsen_US
dc.contributor.external-examinerJoanna Erdmanen_US
dc.contributor.graduate-coordinatorStephen Coughlanen_US
dc.contributor.thesis-readerMichael Hadskisen_US
dc.contributor.thesis-supervisorElaine Gibsonen_US
dc.contributor.ethics-approvalNot Applicableen_US
dc.contributor.manuscriptsNot Applicableen_US
dc.contributor.copyright-releaseNoen_US
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