Viraemia and HIV-1 drug resistance mutations among patients receiving antiretroviral treatment in Mozambique

被引:15
|
作者
Maldonado, F. [2 ]
Biot, M. [2 ]
Roman, F. [3 ]
Masquelier, C. [3 ]
Anapenge, M. [2 ]
Bastos, R. [4 ]
Chuquela, H. C. [5 ]
Arendt, V. [6 ]
Schmit, J. C. [3 ]
Zachariah, R. [1 ]
机构
[1] Med sans Frontieres, Med Dept Operat Res, L-1617 Luxembourg, Luxembourg
[2] Med sans Frontieres, Maputo, Mozambique
[3] Ctr Rech Publ Sante, Retrovirol Lab, L-1526 Luxembourg, Luxembourg
[4] MoH, Cent Hosp Maputo, Maputo, Mozambique
[5] City Hlth Author, Primeiro Maio Hlth Ctr, Maputo, Mozambique
[6] Cent Hosp & Trop Dis Unit, L-1210 Luxembourg, Luxembourg
关键词
HIV; Antiretroviral therapy; Viral Load; Drug resistance; Adherence support; Mozambique; RESOURCE-POOR SETTINGS; DRIED-BLOOD; THERAPY; ADHERENCE; LOAD; PREVENTION; OUTCOMES; PLASMA; BLIPS; CARE;
D O I
10.1016/j.trstmh.2008.07.014
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
This study was conducted among individuals taking first-line antiretroviral treatment (ART) for at least 12 months under programme conditions in Maputo, Mozambique in order to report on the level of detectable viraemia and the proportion and types of drug resistance mutations among those with detectable viral loads. HIV-1 RNA viral toad levels (tower detection limit <50 copies/ml) were measured, and resistance mutations were sequenced. One hundred and forty-nine consecutive patients (69% females, median age 36 years) were included after a mean follow-up time of 23 months. One hundred and seven (72%; 95% CI 64-79) had undetectable viral toad, white in 42 (28%, 95% CI 21-36) viral load was detectable (range 50-58884 copies/ml). From 15 patients with viral load >1000 copies/ml, 12 viruses were sequenced: eight were C subtypes and four were circulating recombinant forms (CRF08). Eight (5%; 95% CI 2-9) patients with detectable viral load had one or more major resistance mutations. Nucleoside reverse transcriptase inhibitor (NRTI) and non-NRTI mutations were observed. There were no major mutations for resistance to protease inhibitors. In Maputo, the level of detectable viraemia is reassuringly tow. While embarking on ART scale-up, wider surveillance is warranted to monitor programme quality and limit the development of drug resistance, which remains a major potential challenge for the future of ART in Africa. (C) 2008 Royal Society of Tropical Medicine and Hygiene. Published by Elsevier Ltd. ALL rights reserved.
引用
收藏
页码:607 / 612
页数:6
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