Population-Based Surveillance of HIV Drug Resistance Emerging on Treatment and Associated Factors at Sentinel Antiretroviral Therapy Sites in Namibia

被引:13
作者
Hong, Steven Y. [1 ,2 ]
Jonas, Anna [3 ]
DeKlerk, Michael [3 ]
Shiningavamwe, Andreas [4 ]
Desta, Tiruneh [3 ]
Badi, Alfons [3 ]
Morris, Lynn [5 ]
Hunt, Gillian M. [5 ]
Ledwaba, Johanna [5 ]
Sheehan, Heidi B. [1 ]
Lau, Kiger [1 ]
Trotter, Andrew [1 ,2 ]
Tang, Alice M. [1 ]
Wanke, Christine [1 ,2 ]
Jordan, Michael R. [1 ,2 ]
机构
[1] Tufts Univ, Sch Med, Dept Publ Hlth & Community Med, Boston, MA 02111 USA
[2] Tufts Med Ctr, Div Geog Med & Infect Dis, Boston, MA USA
[3] Republ Namibia Minist Hlth & Social Serv, Windhoek, Namibia
[4] Namibia Inst Pathol, Mol Diag Unit, Windhoek, Namibia
[5] Natl Inst Communicable Dis, Ctr HIV & STIs, HIV Virol Sect, Johannesburg, South Africa
基金
美国国家卫生研究院;
关键词
HIV; AIDS; Africa; antiretroviral therapy; drug resistance; adherence; VIROLOGICAL FAILURE; PREVENTION; MUTATIONS;
D O I
10.1097/QAI.0000000000000509
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Objective: The World Health Organization (WHO) prospective surveys of acquired HIV drug resistance (HIVDR) evaluate HIVDR emerging after the first year of antiretroviral therapy (ART) and associated factors. Methods: Consecutive ART starters in 2009 were enrolled at 3 sentinel sites in Namibia. Genotyping was performed at start and after 12 months in patients with HIV viral load (VL) >1000 copies per mL. HIVDR outcomes were: HIVDR prevention (VL <= 1000 copies/mL), possible HIVDR (VL >1000 copies/mL without detectable HIVDR or loss to follow-up or ART stop), and HIVDR (VL>1000 copies/mL with detectable HIVDR). Adherence was assessed using medication possession ratio (MPR). Results: Of 394 starters, at 12 months, 80% were on first-line ART, 1% died, 4% transferred out, 1% stopped ART, <1% switched to second-line, and 15% were lost to follow-up. Among patients on first-line, 77% had VL testing, and 94% achieved VL <= 1000 copies per mL. At baseline, 7% had HIVDR. After 12 months, among patients with VL testing, 5% had HIVDR. A majority of patients failing therapy had high-level resistance to nonnucleoside reverse transcriptase inhibitors but none to protease inhibitors. All sites achieved the WHO target of >= 70% HIVDR prevention. Factors associated with not achieving HIVDR prevention were: baseline resistance to nonnucleoside reverse transcriptase inhibitors [odds ratio (OR) 3.0, P = 0.023], WHO stage 3 or 4 at baseline (OR 2.0, P = 0.012), and MPR,75% (OR 4.9, P = 0.021). Conclusions: Earlier ART initiation and removal of barriers to on-time drug pickups may help to prevent HIVDR. These data inform decisions at national and global levels on the effectiveness of first- and second-line regimens.
引用
收藏
页码:463 / 471
页数:9
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