Learning Objectives
Upon completion of this activity, participants should be able to:
- Describe the results of studies investigating the use of boosted PIs in the treatment of pregnant HIV-infected women
- Discuss whether the rate of initial viral decay is associated with long-term virologic outcomes of therapy
- Summarize the results of recent studies utilizing FDA-approved and investigational antiretrovirals as first-line regimens in HIV-infected patients
- Specify considerations that may influence the choice of first-line antiretroviral regimens in resource-limited settings
- Describe recent data on the predictive value of viral load in determining CD4+ cell count decline and disease progression
Topics covered include:
- Use of Boosted PIs in HIV-Infected Pregnant Women
- TMC278 vs Efavirenz Among Treatment-Naive Patients
- Viral Decay With Efavirenz- vs Lopinavir/Ritonavir-Based Therapy in ACTG 5142
- Observational Comparisons of Efavirenz- vs Lopinavir/Ritonavir-Based Regimens
- Once-Daily vs Twice-Daily Lopinavir/Ritonavir in Treatment-Naive Patients
- Tshepo Study: Directly Observed HAART Among Treatment-Naive HIV-Infected Individuals in Botswana
- NORA Study: Abacavir- vs Nevirapine-Based Treatment in Uganda
- GESIDA 3903: Didanosine/Lamivudine vs Zidovudine/Lamivudine With Efavirenz
- Early Virologic Failure With Once-Daily Regimen of Lamivudine, Tenofovir, and Nevirapine
- Baseline Viral Load as a Predictor of HIV Disease Progression
- Influence of Race and Sex on Treatment Outcomes
- Conclusion: Current Directions in First-Line Therapy