Learning Objectives
Upon completion of this activity, participants should be able to:
Discuss treatment outcomes observed in patients initiating antiretroviral therapy in resource-limited countries.
Explain the results of trials investigating outcomes in patients modifying antiretroviral therapy to manage toxicity.
Describe recent data on immunologic parameters for initiation of antiretroviral therapy.
Recount key efficacy and safety data from recent clinical trials comparing first-line antiretroviral regimens.
Topics covered include:
- When to Start
- GS 934: Tenofovir + Emtricitabine vs Zidovudine/Lamivudine for HAART Initiation
- Zidovudine/Lamivudine Plus Tenofovir
- Response to Therapy in Brazil
- GS 903e Extension Study
- OK Study: Maintenance With Lopinavir/Ritonavir Monotherapy
- SWAN Study: Switch to Atazanavir
- Immunologic Responses to Therapy