Page 112 - HIV/AIDS Guidelines
P. 112

Discontinuation or Interruption of Antiretroviral Therapy (Last updated January 10, 2011; last
            reviewed January 10, 2011)

            Discontinuation of antiretroviral therapy (ART) may result in viral rebound, immune decompensation, and
            clinical progression. Unplanned interruption of ART may become necessary because of severe drug toxicity,
            intervening illness, surgery that precludes oral therapy, or unavailability of antiretroviral (ARV) medication.
            Some investigators have studied planned treatment discontinuation strategies in situations or for reasons that
            include: in patients who achieve viral suppression and wish to enhance adherence; to reduce inconvenience,
            long-term toxicities, and costs for patients; or in extensively treated patients who experience treatment failure
            due to resistant HIV, to allow reversion to wild-type virus. Potential risks and benefits of interruption vary
            according to a number of factors, including the clinical and immunologic status of the patient, the reason for
            the interruption, the type and duration of the interruption, and the presence or absence of resistant HIV at the
            time of interruption. Below are brief discussions on what is currently known about the risks and benefits of
            treatment interruption in some of these circumstances.

            Short-Term Therapy Interruptions
            Reasons for short-term interruption (days to weeks) of ART vary and may include drug toxicity; intercurrent
            illnesses that preclude oral intake, such as gastroenteritis or pancreatitis; surgical procedures; or
            unavailability of drugs. Stopping ARV drugs for a short time (i.e., <1 to 2 days) due to medical/surgical
            procedures can usually be done by holding all drugs in the regimen. Recommendations for some other
            scenarios are listed below:

            Unanticipated Need for Short-Term Interruption

            •  When a patient experiences a severe or life-threatening toxicity or unexpected inability to take oral
               medications—all components of the drug regimen should be stopped simultaneously, regardless of drug
               half-life.
            Planned Short Term Interruption (>2–3 days)

            •  When all regimen components have similar half-lives and do not require food for proper
               absorption—all drugs may be given with a sip of water, if allowed; otherwise, all drugs should be
               stopped simultaneously. All discontinued regimen components should be restarted simultaneously.
            •  When all regimen components have similar half-lives and require food for adequate absorption,
               and the patient cannot take anything by mouth for a sustained period of time—temporary
               discontinuation of all drug components is indicated. The regimen should be restarted as soon as the
               patient can resume oral intake.

            •  When the ARV regimen contains drugs with differing half-lives—stopping all drugs simultaneously
               may result in functional monotherapy with the drug with the longest half-life (typically a non-nucleoside
               reverse transcriptase inhibitor [NNRTI]). Options in this circumstance are discussed below. (See
               Discontinuation of efavirenz, etravirine, or nevirapine.)

            Interruption of Therapy after Pregnancy
            ARV drugs for prevention of perinatal transmission of HIV are recommended for all pregnant women,
            regardless of whether they have indications for ART for their own health. Following delivery, considerations
            regarding continuation of the ARV regimen for maternal therapeutic indications are the same as for other
            nonpregnant individuals. The decision of whether to continue therapy after delivery should take into account
            current recommendations for initiation of ART, current and nadir CD4 T-cell counts and trajectory, HIV RNA
            levels, adherence issues, and patient preference.


            Guidelines for the Use of Antiretroviral Agents in HIV-1-Infected Adults and Adolescents        H-19

                            Downloaded from http://aidsinfo.nih.gov/guidelines on 12/8/2012 EST.
   107   108   109   110   111   112   113   114   115   116   117