A 55-year-old woman was recently diagnosed with HIV, with an initial CD4 count of 349 cells/mm3 and an HIV RNA level of 158,780 copies/mL. She is now being seen in clinic 4 weeks later and the plan is to start antiretroviral therapy. There is no evidence of resistance on the baseline genotype resistance assay. You are considering using either tenofovir DF-emtricitabine, tenofovir alafenamide-emtricitabine, or abacavir-lamivudine as the nucleoside reverse transcriptase inhibitor (NRTI) backbone, in combination with a third anchor drug.
Which one of the following is TRUE regarding the NRTI backbone options for this patient as part of the initial antiretroviral therapy regimen?
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Question Last Updated
January 28th, 2025
January 28th, 2025
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Darunavir-Cobicistat-Tenofovir alafenamide-Emtricitabine Symtuza
Dolutegravir-Abacavir-Lamivudine Triumeq
Dolutegravir-Lamivudine Dovato
Dolutegravir-Rilpivirine Juluca
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Efavirenz-Tenofovir DF-Emtricitabine Atripla
Elvitegravir-Cobicistat-Tenofovir alafenamide-Emtricitabine Genvoya
Elvitegravir-Cobicistat-Tenofovir DF-Emtricitabine Stribild
Rilpivirine-Tenofovir alafenamide-Emtricitabine Odefsey
Rilpivirine-Tenofovir DF-Emtricitabine Complera
Fostemsavir Rukobia
Ibalizumab Trogarzo
Maraviroc Selzentry
Dolutegravir Tivicay
Raltegravir Isentress
Tenofovir alafenamide-Emtricitabine Descovy
Tenofovir DF-Emtricitabine Truvada and Multiple Generics
Doravirine Pifeltro
Efavirenz Sustiva
Etravirine Intelence
Rilpivirine Edurant