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  Vol. 301 No. 3, January 21, 2009 TABLE OF CONTENTS
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CDC Recommendations for Opt-Out HIV Testing

Since this article does not have an abstract, we have provided the first 150 words of the full text and any section headings.

To the Editor: In their Special Communication, Dr Bartlett and colleagues1 noted that the benefits and harms of the Centers for Disease Control and Prevention (CDC) recommendations for opt-out testing for human immunodeficiency virus (HIV) in health care settings have yet to be systematically assessed. Although the authors listed some possible metrics, their suggestions did not emphasize several critical potential outcomes and effects of opt-out testing.

I believe that the metrics must include the following: (1) percentage of persons living with HIV aware of their serostatus; (2) percentage of persons newly diagnosed with HIV receiving high-quality, comprehensive health care that includes, but is not limited to, HIV-specific services; (3) percentage of persons testing positive who receive evidence-based, patient-centered HIV prevention services to avoid transmission; (4) percentage of persons testing HIV seronegative but at imminent risk of infection who receive evidence-based, patient-centered HIV prevention services; (5) percentage of persons (stratified by . . . [Full Text of this Article]

David R. Holtgrave, PhD
dholtgrave@jhsph.edu
Department of Health, Behavior and Society
Johns Hopkins Bloomberg School of Public Health
Baltimore, Maryland



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RELATED ARTICLE

Opt-Out Testing for Human Immunodeficiency Virus in the United States: Progress and Challenges
John G. Bartlett, Bernard M. Branson, Kevin Fenton, Benjamin C. Hauschild, Veronica Miller, and Kenneth H. Mayer
JAMA. 2008;300(8):945-951.
ABSTRACT | FULL TEXT  

RELATED LETTERS

CDC Recommendations for Opt-Out HIV Testing
Lawrence Corey
JAMA. 2009;301(3):274-275.
EXTRACT | FULL TEXT  

CDC Recommendations for Opt-Out HIV Testing—Reply
John G. Bartlett and Kenneth Hugh Mayer
JAMA. 2009;301(3):275-276.
EXTRACT | FULL TEXT  






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