Viremia and drug resistance among HIV-1 patients on antiretroviral treatment: a cross-sectional study in Soweto, South Africa

被引:95
|
作者
El-Khatib, Ziad [1 ,2 ]
Ekstrom, Anna Mia [1 ]
Ledwaba, Johanna [2 ]
Mohapi, Lerato [3 ]
Laher, Fatima [3 ]
Karstaedt, Alan [4 ,5 ]
Charalambous, Salome [6 ]
Petzold, Max [1 ,7 ]
KatzensteinG, David [8 ]
Morris, Lynn [2 ]
机构
[1] Karolinska Inst, Div Global Hlth IHCAR, SE-17177 Stockholm, Sweden
[2] NICD, AIDS Virus Res Unit, Johannesburg, South Africa
[3] Univ Witwatersrand, PHRU, Soweto, South Africa
[4] Chris Hani Baragwanath Hosp, Div Infect Dis, Johannesburg, South Africa
[5] Univ Witwatersrand, Johannesburg, South Africa
[6] Aurum Inst Hlth, Johannesburg, South Africa
[7] Nord Sch Publ Hlth NHV, Gothenburg, Sweden
[8] Stanford Univ, Div Infect Dis, Stanford, CA 94305 USA
关键词
adherence; antiretroviral therapy; HIV; HIV drug resistance; South Africa; viral failure; SUB-SAHARAN AFRICA; VIROLOGICAL FAILURE; INFECTED ADULTS; THERAPY; ADHERENCE; RISK; CARE;
D O I
10.1097/QAD.0b013e32833a097b
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background: We assessed risk factors for viremia and drug resistance among long-term recipients of antiretroviral therapy (ART) in South Africa. Methods: In 2008, we conducted a cross-sectional study among patients receiving ART for 12 months or more. Genotypic resistance testing was performed on individuals with a viral load higher than 400 RNA copies/ml. Multiple logistic regression analysis was used to assess associations. Results: Of 998 participants, 75% were women with a median age of 41 years. Most (64%) had been on treatment for more than 3 years. The prevalence of viremia was 14% (n=139): 12% (102/883) on first-line [i.e. nonnucleoside reverse-transcriptase inhibitor (NNRTI)-based regimen] and 33% (37/115) on second-line (i.e. protease inhibitor (PI)-based regimen) ART. Of viremic patients, 78% had drug resistance mutations. For NRTIs, NNRTIs and PIs, the prevalence of mutations was 64, 81 and 2%, respectively, among first-line failures and 29, 54 and 6%, respectively, among second-line failures. M184V/I, K103N and V106A/M were the most common mutations. Significant risk factors associated with viremia on first-line regimen included concurrent tuberculosis treatment [odds ratio (OR) 6.4, 95% confidence interval (CI) 2.2-18.8, P<0.01] and a recent history of poor adherence (OR 2.7, 1.3-5.6, P=0.01). Among second-line failures, attending a public clinic (OR 4.6, 95% CI 1.8-11.3, P<0.01) and not having a refrigerator at home (OR 6.7, 95% CI 1.2-37.5, P=0.03) were risk factors for virological failure. Conclusion: Risk factors for viral failure were line regimen dependent. Second-line ART recipients had a higher rate of viremia, albeit with infrequent PI drug resistance mutations. Measures to maintain effective virologic suppression should include increased adherence counseling, attention to concomitant tuberculosis treatment and heat-stable formulations of second-line ART regimens. (C) 2010 Wolters Kluwer Health vertical bar Lippincott Williams & Wilkins
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页码:1679 / 1687
页数:9
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