Ontology highlight
ABSTRACT: Background
Previous studies suggest that nonnucleoside reverse-transcriptase inhibitors (NNRTIs) cause faster virologic suppression, while ritonavir-boosted protease inhibitors (PI/r) recover more CD4 cells. However, individual trials have not been powered to compare clinical outcomes.Methods
We searched databases to identify randomized trials that compared NNRTI- vs PI/r-based initial therapy. A metaanalysis calculated risk ratios (RRs) or mean differences (MDs), as appropriate. Primary outcome was death or progression to AIDS. Secondary outcomes were death, progression to AIDS, and treatment discontinuation. We calculated RR of virologic suppression and MD for an increase in CD4 cells at week 48.Results
We included 29 trials with 9047 participants. Death or progre
SUBMITTER: Borges AH
PROVIDER: S-EPMC6276924 | biostudies-literature | 2016 Jul
REPOSITORIES: biostudies-literature