Le SIDA au Ghana (serveur d'exploration)

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CULTURE AND VOLUNTARY INFORMED CONSENT IN AFRICAN HEALTH CARE SYSTEMS

Identifieur interne : 000C06 ( Main/Curation ); précédent : 000C05; suivant : 000C07

CULTURE AND VOLUNTARY INFORMED CONSENT IN AFRICAN HEALTH CARE SYSTEMS

Auteurs : Augustine Frimpong-Mansoh [États-Unis]

Source :

RBID : ISTEX:4174DA9ED53BB939224B1365863EC0F4FC69A6D6

Descripteurs français

English descriptors

Abstract

This paper discusses how to apply a collective decision model of the principle of voluntary informed consent in African communitarian culture, in a culturally sensitive way, in order to protect research candidates from potential exploitations and abuses. Dismissing cultural and ethical skepticism surrounding the global application of the principle of voluntary informed consent, the paper ultimately concludes that international collaboration on diagnostic and therapeutic medical research in Africa, especially HIV vaccine trials, is a moral imperative.

Url:
DOI: 10.1111/j.1471-8847.2006.00181.x

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ISTEX:4174DA9ED53BB939224B1365863EC0F4FC69A6D6

Le document en format XML

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<term>Human beings</term>
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<term>Human virus</term>
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<term>Individual patient</term>
<term>Individual patients</term>
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<term>Bioethical</term>
<term>Bioethical principle</term>
<term>Bioethics</term>
<term>Biomedical ethics</term>
<term>Blackwell</term>
<term>Blackwell publishing</term>
<term>Chronic diseases</term>
<term>Clinical trials</term>
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<term>Communitarian values</term>
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<term>Contemporary africa</term>
<term>Contemporary societies</term>
<term>Cultural beliefs</term>
<term>Cultural norms</term>
<term>Cultural sensitivity</term>
<term>Cultural space</term>
<term>Cultural values</term>
<term>Cultural variations</term>
<term>Effective implementation</term>
<term>Empirical reality</term>
<term>Ethical acceptability</term>
<term>Ethical guidelines</term>
<term>Ethical imperialism</term>
<term>Ethical skepticism</term>
<term>Global application</term>
<term>Health care</term>
<term>Health care systems</term>
<term>Hopeless health conditions</term>
<term>Human beings</term>
<term>Human nature</term>
<term>Human research subjects</term>
<term>Human rights</term>
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<term>Human virus</term>
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<term>Individual members</term>
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<term>Individual patients</term>
<term>Individual person</term>
<term>Individual persons</term>
<term>Individual rights</term>
<term>Individualistic values</term>
<term>International covenant</term>
<term>International research</term>
<term>Intrinsic respect</term>
<term>Jacquelyn kegley</term>
<term>Journal compilation</term>
<term>Keymanthri moodley</term>
<term>Local community</term>
<term>Medical decisions</term>
<term>Medical patients</term>
<term>Medical research</term>
<term>National bioethics</term>
<term>Nuremberg code</term>
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<term>Personal autonomy</term>
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<term>Potential research candidates</term>
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<div type="abstract" xml:lang="en">This paper discusses how to apply a collective decision model of the principle of voluntary informed consent in African communitarian culture, in a culturally sensitive way, in order to protect research candidates from potential exploitations and abuses. Dismissing cultural and ethical skepticism surrounding the global application of the principle of voluntary informed consent, the paper ultimately concludes that international collaboration on diagnostic and therapeutic medical research in Africa, especially HIV vaccine trials, is a moral imperative.</div>
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