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A rapid review of rapid HIV antibody tests

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TLDR
The operating and performance characteristics, quality assurance and laboratory requirements, and HIV counseling implications of the currently available rapid HIV tests are reviewed.
Abstract
Rapid HIV antibody tests recently approved by the Food and Drug Administration can help reduce unrecognized infections by improving access to testing in both clinical and nonclinical settings and increase the proportion of those tested who learn their results. Four rapid HIV antibody tests are now available in the United States; two are approved for use at point-of-care sites outside a traditional laboratory. All four tests are interpreted visually. Sites offering rapid HIV testing must periodically run external controls (known HIV-positive and HIV-negative specimens) and provide persons who undergo rapid testing a subject information sheet. This paper reviews the operating and performance characteristics, quality assurance and laboratory requirements, and HIV counseling implications of the currently available rapid HIV tests.

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References
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Journal ArticleDOI

HIV Prevalence and Associated Risks in Young Men Who Have Sex With Men

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Journal ArticleDOI

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TL;DR: Ambulatory care visits made to physician offices in the United States are described on selected characteristics of the physician's practice, the patient, and the visit, which highlights visits to primary care specialties.
Book

No Time to Lose: Getting More from HIV Prevention

TL;DR: The No Time to Lose framework as discussed by the authors is a framework for a national prevention strategy to prevent new HIV infections in the United States, based on the Institute of Medicine's No Time To Lose framework.
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Rapid HIV-1 testing during labor: a multicenter study.

TL;DR: Rapid HIV testing is feasible and delivers accurate and timely test results for women in labor, proven to reduce perinatal HIV transmission, and may be particularly applicable to higher-risk populations.
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