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Virologic Response to First-line Efavirenz-or Nevirapine-based Antiretroviral Therapy in HIV-infected African Children

Virologic Response to First-line Efavirenz-or Nevirapine-based Antiretroviral Therapy in HIV-infected African Children

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dc.contributor.author Kekitiinwa, Adeodata
dc.contributor.author Szubert, Alexander J.
dc.contributor.author Spyer, Moira
dc.contributor.author Katuramu, Richard
dc.contributor.author Musiime, Victor
dc.contributor.author Mhute, Tawanda
dc.contributor.author Bakeera-Kitaka, Sabrina
dc.contributor.author Senfuma, Oscar
dc.contributor.author Walker, Ann Sarah
dc.contributor.author Gibb, Diana M.
dc.date 2999
dc.date.accessioned 2021-01-01T21:58:25Z
dc.date.available 2021-01-01T21:58:25Z
dc.identifier.issn 0891-3668
dc.identifier.uri http://combine.alvar.ug/handle/1/48305
dc.description.abstract Background: Poorer virologic response to nevirapine- versus efavirenz-based antiretroviral therapy (ART) has been reported in adult systematic reviews and pediatric studies. Methods: We compared drug discontinuation and viral load (VL) response in ART-naive Ugandan/Zimbabwean children >= 3 years of age initiating ART with clinician-chosen nevirapine versus efavirenz in the ARROW trial. Predictors of suppression <80, <400 and <1000 copies/mL at 36, 48 and 144 weeks were identified using multivariable logistic regression with backwards elimination (P = 0.1). Results: A total of 445 (53%) children received efavirenz and 391 (47%) nevirapine. Children receiving efavirenz were older (median age, 8.6 vs. 7.5 years nevirapine, P < 0.001) and had higher CD4% (12% vs. 10%, P = 0.05), but similar pre-ART VL (P = 0.17). The initial non-nucleoside-reverse-transcriptase-inhibitor (NNRTI) was permanently discontinued for adverse events in 7 of 445 (2%) children initiating efavirenz versus 9 of 391 (2%) initiating nevirapine (P = 0.46); at switch to second line in 17 versus 23, for tuberculosis in 0 versus 26, for pregnancy in 6 versus 0 and for other reasons in 15 versus 5. Early (36-48 weeks) virologic suppression <80 copies/mL was superior with efavirenz, particularly in children with higher pre-ART VL (P = 0.0004); longer-term suppression was superior with nevirapine in older children (P = 0.05). Early suppression was poorer in the youngest and oldest children, regardless of NNRTI (P = 0.02); longer-term suppression was poorer in those with higher pre-ART VL regardless of NNRTI (P = 0.05). Results were broadly similar for <400 and <1000 copies/mL. Conclusion: Short-term VL suppression favored efavirenz, but long-term relative performance was age dependent, with better suppression in older children with nevirapine, supporting World Health Organization recommendation that nevirapine remains an alternative NNRTI.
dc.description.sponsorship UK Medical Research CouncilMedical Research Council UK (MRC)
dc.description.sponsorship UK Department for International Development (DFID)
dc.description.sponsorship Medical Research CouncilMedical Research Council UK (MRC) [MC_EX_G0300400, MC_UU_12023/26] Funding Source: researchfish
dc.language English
dc.publisher LIPPINCOTT WILLIAMS & WILKINS
dc.relation.ispartof Pediatric Infectious Disease Journal
dc.subject Hiv
dc.subject Children
dc.subject Antiretroviral Therapy
dc.subject Viral Load
dc.subject Nnrti
dc.title Virologic Response to First-line Efavirenz-or Nevirapine-based Antiretroviral Therapy in HIV-infected African Children
dc.type Article
dc.identifier.isi 000403213800012
dc.identifier.doi 10.1097/INF.0000000000001505
dc.identifier.pmid 2815
dc.publisher.city PHILADELPHIA
dc.publisher.address TWO COMMERCE SQ, 2001 MARKET ST, PHILADELPHIA, PA 19103 USA
dc.identifier.eissn 1532-0987
dc.identifier.volume 36
dc.identifier.issue 6
dc.identifier.spage 588
dc.identifier.epage 594
dc.subject.wc Immunology
dc.subject.wc Infectious Diseases
dc.subject.wc Pediatrics
dc.subject.sc Immunology
dc.subject.sc Infectious Diseases
dc.subject.sc Pediatrics
dc.description.oa Green Accepted
dc.description.oa Green Published
dc.description.pages 7
dc.contributor.group ARROW Trial Team
dc.subject.kwp Thai Children
dc.subject.kwp Failure
dc.subject.kwp Regimens
dc.subject.kwp Adolescents
dc.subject.kwp Predictors
dc.subject.kwp Models
dc.subject.kwp Time
dc.description.affiliation Mulago Hosp, Baylor Uganda Paediat Infect Dis Clin, Kampala, Uganda
dc.description.affiliation UCL, MRC Clin Trials Unit, London, England
dc.description.affiliation Uganda Virus Res Inst, Uganda Res Unit AIDS, MRC, Entebbe, Uganda
dc.description.affiliation Joint Clin Res Ctr, Kampala, Uganda
dc.description.affiliation Makerere Univ, Coll Hlth Sci, Kampala, Uganda
dc.description.affiliation Univ Zimbabwe, Coll Hlth Sci, Harare, Zimbabwe
dc.description.email a.szubert@ucl.ac.uk
dc.description.corr Szubert, AJ (corresponding author), UCL, MRC Clin Trials Unit, Inst Clin Trials & Methodol, London WC2B 6NH, England.


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