Routine screening: Informed consent, stigma and the waning of HIV exceptionalism
American Journal of Bioethics 6 (4):5 – 8 (2006)
| Abstract | The Centers for Disease Control and Prevention (CDC) recently recommended that HIV screening should become routine for all adults in the United States. Implicit in the CDC proposal is the notion that pre-test counseling would be more limited than at present, and that written informed consent to screening would no longer be required. If widely implemented, routine testing would mark a tremendous shift in the US HIV screening strategy. There are a number of considerations used to determine what screening tests should be routine, and HIV fits the bill in almost every regard. Yet the stigma associated with HIV infection remains, making the CDC's recommendation highly controversial. Will minimizing requirements for pre-test counseling and special written informed consent lead to unexpected or unwanted HIV testing, or do these stringent counseling and consent requirements needlessly scare people away? Will widespread and routine testing be associated with declining stigmatization, or will it drive some patients away from seeking desperately needed health care? These are high stakes questions, and we're about to find out the answers. | |||||||||
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Sofia Gruskin, Shahira Ahmed & Laura Ferguson (2008). Provider-Initiated Hiv Testing and Counseling in Health Facilities – What Does This Mean for the Health and Human Rights of Pregnant Women? Developing World Bioethics 8 (1):23–32.
Timothy F. Murphy (1994). Health Care Workers with Hiv and a Patient's Right to Know. Journal of Medicine and Philosophy 19 (6):553-569.
P. de Zulueta & M. Boulton (2007). Routine Antenatal HIV Testing: The Responses and Perceptions of Pregnant Women and the Viability of Informed Consent. A Qualitative Study. Journal of Medical Ethics 33 (6):329-336.
David J. Mayo, Frank S. Rhame & Martin Gunderson (1996). Routine HIV Testing of Hospital Patients and Pregnant Women: Informed Consent in the Real World. Kennedy Institute of Ethics Journal 6 (2):161-182.
Loretta M. Kopelman (1994). Informed Consent and Anonymous Tissue Samples: The Case of Hiv Seroprevalence Studies. Journal of Medicine and Philosophy 19 (6):525-552.
Michael Waxman, Roland Merchant, M. Celada & Melissa Clark (2011). Perspectives on the Ethical Concerns and Justifications of the 2006 Centers for Disease Control and Prevention HIV Testing Recommendations. BMC Medical Ethics (1):24-.
R. Bennett (2007). Routine Antenatal HIV Testing and Informed Consent: An Unworkable Marriage? Journal of Medical Ethics 33 (8):446-448.
Thaddeus Metz (2005). The Ethics of Routine HIV Testing: A Respect-Based Analysis. South African Journal on Human Rights 21 (3):370-405.
Matthew W. Pierce, Suzanne Maman, Allison K. Groves, Elizabeth J. King & Sarah C. Wyckoff (2011). Testing Public Health Ethics: Why the CDC's HIV Screening Recommendations May Violate the Least Infringement Principle. Journal of Law, Medicine and Ethics 39 (2):263-271.
Martin Gunderson, David J. Mayo & Frank S. Rhame (1996). Routine HIV Testing of Hospital Patients and Pregnant Women: Informed Consent in the Real World. Kennedy Institute of Ethics Journal 6 (2).
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