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  1. HIV prevention research and global inequality: steps towards improved standards of care.K. Shapiro - 2005 - Journal of Medical Ethics 31 (1):39-47.
    Next SectionIntensification of poverty and degradation of health infrastructure over recent decades in countries most affected by HIV/AIDS present formidable challenges to clinical research. This paper addresses the overall standard of health care (SOC) that should be provided to research participants in developing countries, rather than the narrow definition of SOC that has characterised the international debate on standards of health care. It argues that contributing to sustainable improvements in health by progressively ratcheting the standard of care upwards for research (...)
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  • Public Health Ethics: Mapping the Terrain.James F. Childress, Ruth R. Faden, Ruth D. Gaare, Lawrence O. Gostin, Jeffrey Kahn, Richard J. Bonnie, Nancy E. Kass, Anna C. Mastroianni, Jonathan D. Moreno & Phillip Nieburg - 2002 - Journal of Law, Medicine and Ethics 30 (2):170-178.
    Public health ethics, like the field of public health it addresses, traditionally has focused more on practice and particular cases than on theory, with the result that some concepts, methods, and boundaries remain largely undefined. This paper attempts to provide a rough conceptual map of the terrain of public health ethics. We begin by briefly defining public health and identifying general features of the field that are particularly relevant for a discussion of public health ethics.Public health is primarily concerned with (...)
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  • Facing Ethical Challenges in Rolling Out Antiretroviral Treatment in Resource-Poor Countries: Comment on “They Call It ‘Patient Selection’ in Khayelitsha”.Solomon Benatar - 2006 - Cambridge Quarterly of Healthcare Ethics 15 (3):322-330.
    It is widely acknowledged that the HIV and AIDS pandemic is a global emergency and that cheap, effective treatment should be provided for as many people as possible worldwide. But there are many challenges to rolling out antiretroviral treatment in resource-poor settings. These include the cost of drugs, sustaining their supply and distribution, the complexity of treatment regimens, selection of patients for treatment, shortage of medical and nursing personnel, inadequacy of healthcare facilities, the need for uninterrupted, lifelong treatment, and monitoring (...)
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  • Inclusion: The Politics of Difference in Medical Research.Steven Epstein - 2008 - International Journal of Feminist Approaches to Bioethics 1 (2):174-178.
     
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  • Participation in biomedical research: The consent process as viewed by children, adolescents, young adults, and physicians.John C. Fletcher - forthcoming - Research Ethics.
     
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