Best practices for integrating
human immunodeficiency virus (HIV) testing and antiretroviral interventions for
prevention and treatment are suggested based on research evidence and existing
normative guidance. The goal is to provide high-impact prevention services
during periods of substantial risk. Antiretroviral medications are recommended
for postexposure prophylaxis (PEP), pre-exposure prophylaxis (PrEP), and
treatment of HIV infection. We reviewed research evidence and current normative
guidelines to identify best practices for integrating these high-impact
prevention strategies. More sensitive HIV tests used for screening enable
earlier diagnosis and treatment of HIV infection, more appropriate counseling,
and help limit drug resistance. A fully suppressive PEP regimen should be initiated
based on exposure history or physical findings when sensitive diagnostic
testing is delayed or not available and antibody tests are negative.
Transitions from PEP to PrEP are often warranted because HIV exposure events
may continue to occur. This algorithmic approach to integrating PEP, PrEP, and
early treatment decisions may increase the uptake of these interventions by a
greater number and diversity of knowledgeable healthcare providers.
Below: An integrated postexposure
prophylaxis (PEP), pre-exposure prophylaxis (PrEP), and treatment transition
algorithm. In people reporting mucosal exposure to fluids likely to be infected
with human immunodeficiency virus (HIV) in the past 72 hours, start PEP with a
3-drug regimen while awaiting the results of HIV testing. In people with
repeated HIV exposures, a negative HIV antibody test, and no signs or symptoms
consistent with acute HIV infection, start PrEP with emtricitabine/tenofovir
disoproxil fumarate (FTC/TDF). A negative test for HIV nucleic acids or antigen
is preferred, especially if there are signs or symptoms of an acute viral
syndrome. If any HIV test is positive, initiate antiretroviral therapy without
delay and send specimens for HIV-confirmatory and drug-resistance testing as
soon as possible.
Below: Sequence of appearance of
laboratory markers of human immunodeficiency virus (HIV) infection. The figure
is from the updated Centers for Disease Control and Prevention (CDC) guidelines
for HIV testing and was adapted from prior publications [36–41].
Full article
at: http://goo.gl/mA1WlW
By: Robert M. Grant1,2 and Dawn K. Smith3
1Gladstone Institutes and University of
California, San Francisco
2San Francisco AIDS Foundation, California
3Division of HIV/AIDS Prevention, Centers
for Disease Control and Prevention, Atlanta, Georgia
Correspondence: Robert M. Grant, MD, MPH, Gladstone
Institutes and University of California, San Francisco, 1650 Owens St., San
Francisco, CA 94158 (Email: ude.fscu@tnarg.trebor
More at: https://twitter.com/hiv_insight


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