Risk of extended viral resistance in human immunodeficiency virus-1-infected Mozambican children after first-line treatment failure
Pediatr. infect. dis. j; 28 (12), 2009
Ano de publicação: 2009
Background:
Resistant virus may be selected by sub-optimal control of HIV-1 replication during antiretroviral treatment. The incidence and profile of resistance in children receiving World Health Organization-recommended treatment remains to be evaluated on a large scale.Goals:
Assessment of the frequency and profile of resistant virus in HIV-1-infected children, treated for at least 6 months with stavudine/zidovudine + lamivudine + nevirapine and presenting virological failure in a large access program in Maputo, Mozambique.Results:
Cross-sectional evaluation of plasma HIV-1 viral load (VL) in 495 evaluable children among 512 treated for at least 6 months showed that 360 (72.7%) had a VL of <50 copies/mL of HIV-1 RNA. Genotypic resistance tests were performed in the 84 available samples from the 135 treated children with VL > or = 50 copies/mL: 92% of the viruses were resistant to lamivudine and/or nevirapine, and 15% were resistant to stavudine. Twenty children (24%) harbored virus with a extended spectrum of cross-resistance defined as resistance to the 3 drugs of the combination received by the child and/or at least 1 resistance to a drug to which the child had never been exposed (abacavir: 5%, tenofovir: 6%, didanosine: 3.5% and the new generation non nucleoside inhibitor, etravirine: 6%). The only factor identified by multivariate analysis as being associated with this extended resistance profile was the duration of treatment (aOR: 6.67 [95% CI: 1.24-35.93], P = 0.015 for treatment >24 months) with a per month increase of 1.09 (1.02-1.16) P = 0.007.
Resistência a Medicamentos, HIV-1/genética, Fármacos Anti-HIV, Infecções por HIV/sangue, Replicação Viral, Análise de Variância, HIV-1/fisiologia, Infecções por HIV/terapia, Infecções por HIV/virologia, Inibidores da Transcriptase Reversa/farmacologia, Inibidores da Transcriptase Reversa/uso terapêutico, Fármacos Anti-HIV/farmacologia, Fármacos Anti-HIV/uso terapêutico, Falha de Tratamento, Moçambique