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. |
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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 |
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dc.language |
English |
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dc.publisher |
LIPPINCOTT WILLIAMS & WILKINS |
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dc.relation.ispartof |
Pediatric Infectious Disease Journal |
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dc.subject |
Hiv |
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dc.subject |
Children |
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dc.subject |
Antiretroviral Therapy |
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dc.subject |
Viral Load |
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dc.subject |
Nnrti |
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dc.title |
Virologic Response to First-line Efavirenz-or Nevirapine-based Antiretroviral Therapy in HIV-infected African Children |
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dc.type |
Article |
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dc.identifier.isi |
000403213800012 |
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dc.identifier.doi |
10.1097/INF.0000000000001505 |
|
dc.identifier.pmid |
2815 |
|
dc.publisher.city |
PHILADELPHIA |
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dc.publisher.address |
TWO COMMERCE SQ, 2001 MARKET ST, PHILADELPHIA, PA 19103 USA |
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dc.identifier.eissn |
1532-0987 |
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dc.identifier.volume |
36 |
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dc.identifier.issue |
6 |
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dc.identifier.spage |
588 |
|
dc.identifier.epage |
594 |
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dc.subject.wc |
Immunology |
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dc.subject.wc |
Infectious Diseases |
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dc.subject.wc |
Pediatrics |
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dc.subject.sc |
Immunology |
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dc.subject.sc |
Infectious Diseases |
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dc.subject.sc |
Pediatrics |
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dc.description.oa |
Green Accepted |
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dc.description.oa |
Green Published |
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dc.description.pages |
7 |
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dc.contributor.group |
ARROW Trial Team |
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dc.subject.kwp |
Thai Children |
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dc.subject.kwp |
Failure |
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dc.subject.kwp |
Regimens |
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dc.subject.kwp |
Adolescents |
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dc.subject.kwp |
Predictors |
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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 |
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dc.description.corr |
Szubert, AJ (corresponding author), UCL, MRC Clin Trials Unit, Inst Clin Trials & Methodol, London WC2B 6NH, England. |
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