Drug resistance is widespread among children who receive long-term antiretroviral treatment at a rural Tanzanian hospital

被引:20
作者
Bratholm, Clara [1 ,2 ]
Johannessen, Asgeir [1 ]
Naman, Ezra [3 ]
Gundersen, Svein G. [4 ,5 ]
Kivuyo, Sokoine L. [6 ]
Holberg-Petersen, Mona [7 ]
Ormaasen, Vidar [1 ]
Bruun, Johan N. [1 ,8 ,9 ]
机构
[1] Oslo Univ Hosp, Dept Infect Dis, Oslo, Norway
[2] Univ Oslo, Fac Med, Oslo, Norway
[3] Haydom Lutheran Hosp, HIV Care & Treatment Ctr, Mbulu, Tanzania
[4] Sorlandet Hosp HF, Res Unit, Kristiansand, Norway
[5] Univ Agder, Ctr Dev Studies, Kristiansand, Norway
[6] Natl Inst Med Res, Dar Es Salaam, Tanzania
[7] Oslo Univ Hosp, Dept Microbiol, Oslo, Norway
[8] Univ Tromso, Inst Clin Med, Tromso, Norway
[9] Univ Hosp N Norway, Dept Med, Tromso, Norway
关键词
HIV infections; antiretroviral therapy; sub-Saharan Africa; child; HIV-1-INFECTED CHILDREN; THERAPY; EFFICACY;
D O I
10.1093/jac/dkq234
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Objectives: To assess long-term virological efficacy and the emergence of drug resistance in children who receive antiretroviral treatment (ART) in rural Tanzania. Patients and methods: Haydom Lutheran Hospital has provided ART to HIV-infected individuals since 2003. From February through May 2009, a cross-sectional virological efficacy survey was conducted among children (, 15 years) who had completed >= 6 months of first-line non-nucleoside reverse transcriptase inhibitor (NNRTI)-based ART. Genotypic resistance was determined in those with a viral load of >200 copies/mL. Results: Virological response was measured in 19 of 23 eligible children; 8 of 19 were girls and median age at ART initiation was 5 years (range 2-14 years). Median duration of ART at the time of the survey was 40 months (range 11-61 months). Only 8 children were virologically suppressed (<= 40 copies/mL), whereas 11 children had clinically relevant resistance mutations in the reverse transcriptase gene. The most frequent mutations were M184V (n=11), conferring resistance to lamivudine and emtricitabine, and Y181C (n=4), G190A/S (n=4) and K103N (n=4), conferring resistance to NNRTIs. Of concern, three children had thymidine analogue mutations, associated with cross-resistance to all nucleoside reverse transcriptase inhibitors. Despite widespread resistance, however, only one child experienced a new WHO stage 4 event and none had a CD4 cell count of <200 cells/mm(3). Conclusions: Among children on long-term ART in rural Tanzania, >50% harboured drug resistance. Results for children were markedly poorer than for adults attending the same programme, underscoring the need for improved treatment strategies for children in resource-limited settings.
引用
收藏
页码:1996 / 2000
页数:5
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