When compared with the standard approach of continuing lopinavir/ritonavir-based therapy, switching to an efavirenz-based regimen was safe and did not compromise virologic suppression.
Lopinavir/ritonavir therapy is the currently recommended first-line treatment for HIV-infected children. Lopinavir/r syrup, which is administered twice daily, tastes unpleasant, requires cold storage, and can result in metabolic toxicities with long-term use. In a randomized, open-label, noninferiority trial conducted in South Africa, researchers assessed whether HIV-infected children who had previously been exposed to nevirapine for prevention of mother-to-child transmission and had achieved suppression on lopinavir/r-based therapy could be transitioned to an efavirenz-based regimen without increased risk for virologic failure.
By 48 weeks, 3% (4/150) of efavirenz-group children and 2% (3/148) of lopinavir/r-group children had experienced v…
Reviewing Author
DisclosuresConsultant/Advisory BoardUNAIDS; WHO; Bill and Melinda Gates Foundation, Population Council
Grant/Research SupportNIH; National Institute of Allergy and Infectious Diseases; Tides Foundation/MAC AIDS Fund; USAID; South African National Research Foundation; European Union; South African Medical Research Council
Editorial BoardsNew England Journal of Medicine; AIDS Reviews; AIDS Research and Human Retroviruses; mBio; Indian Journal of Medical Research; JAIDS: Journal of Acquired Immune Deficiency Syndromes
DisclosuresConsultant/Advisory BoardUNAIDS; WHO; Bill and Melinda Gates Foundation, Population Council
Grant/Research SupportNIH; National Institute of Allergy and Infectious Diseases; Tides Foundation/MAC AIDS Fund; USAID; South African National Research Foundation; European Union; South African Medical Research Council
Editorial BoardsNew England Journal of Medicine; AIDS Reviews; AIDS Research and Human Retroviruses; mBio; Indian Journal of Medical Research; JAIDS: Journal of Acquired Immune Deficiency Syndromes