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Resistance testing also can help guide treatment decisions for patients with suboptimal viral load reduction
            (AII). Virologic failure in the setting of combination ART is, for certain patients, associated with resistance
            to only one component of the regimen. 44-46  In that situation, substituting individual drugs in a failing regimen
            might be possible, although this concept will require clinical validation. (See Virologic and Immunologic
            Failure.)
            Genotypic testing is generally preferred for virologic failure or suboptimal viral load reduction in persons
            failing their first or second ARV drug regimen because of lower cost, faster turnaround time, and greater
            sensitivity for detecting mixtures of wild-type and resistant virus (AIII). Addition of phenotypic to genotypic
            testing is generally preferred for persons with known or suspected complex drug-resistance mutation
            patterns, particularly to PIs (BIII).

            In patients failing INSTI-based regimens, testing for INSTI resistance should be considered to determine
            whether to include drugs from this class in subsequent regimens; genotypic testing is preferred (BIII).
            Although it is not a drug-resistance assay, a coreceptor tropism assay should be performed whenever the use
            of a CCR5 antagonist is being considered (AI). Coreceptor tropism testing should also be considered for
            patients who exhibit virologic failure on a CCR5 antagonist (CIII). However, such testing may be of limited
            value because the absence of detectable CXCR4-using virus does not exclude the possibility that CCR5
            antagonist resistance may have developed. Assays for detecting resistance to CCR5 antagonists are not yet
                                  47
            commercially available. (See Coreceptor Tropism Assays.)
            Use of Resistance Assays in Pregnant Women
            In pregnant women, the goal of ART is to maximally reduce plasma HIV RNA to provide appropriate
            maternal therapy and prevent mother-to-child transmission (MTCT) of HIV. Genotypic resistance testing is
            recommended for all pregnant women prior to initiation of therapy (AIII) and for those entering pregnancy
            with detectable HIV RNA levels while on therapy (AI). Phenotypic testing may provide additional
            information in those found to have complex drug-resistance mutation patterns, particularly to PIs (BIII).
            Optimal prevention of perinatal transmission may require initiation of ART while results of resistance testing
            are pending. Once the results are available, the ARV regimen can be changed as needed.





































            Guidelines for the Use of Antiretroviral Agents in HIV-1-Infected Adults and Adolescents        C-11

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