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last
update February 2003
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| General
Guidelines |
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The
following recommendations are based on our current understanding
of the pathophysiology of HIV disease and the results of clinical
trials. They reflect updated guidelines of US Department of Health
and Human Services (DHHS) and the International AIDS Society USA
Panel (see links below).
- The primary goal of antiretroviral
therapy should be "to keep the viral load as low as possible for
as long as possible."
- Maximal suppression of the virus makes it
more difficult for resistance to develop.
- Partial suppression results in the
emergence of "quasi-species," which are pre-existing, resistant
mutant strains in the viral population; these arise because of the
rapid turnover of HIV and the many random errors made during
replication.
- Approximately two-thirds of patients on
combination antiretroviral therapy have an undetectable viral load
in response to initial treatment; second and subsequent attempts
at viral suppression are less often successful.
- Current antiretroviral drugs are not
thought to be curative because of the persistence of HIV in latent
CD4 lymphocytes and "sanctuary sites," which are regions of the
body, such as the central nervous system and gonads, in which some
agents do not penetrate well.
- Combination antiretroviral therapy is now
considered the standard of care for HIV infection.
- Sixteen antiretroviral agents have been approved to date
by the Food and Drug Administration.
- Antiretroviral agents (Table
1) are classified by their mode of action against the virus
into the following categories:
- nucleoside reverse transcriptase
inhibitors (NRTIs)
- non-nucleoside reverse transcriptase
inhibitors (NNRTIs)
- protease inhibitors (PIs)
- Antiretroviral agents vary considerably in their dosing
and frequency of administration; how they should be given
(with food or when fasting); their side-effect profiles; and
their potential interactions with other drugs.
DHHS
HIV/AIDS Treatment Information Service
International AIDS
Society
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