Isoniazid preventive therapy, HAART and tuberculosis risk in HIV-infected adults in South Africa: a prospective cohort

被引:179
|
作者
Golub, Jonathan E. [1 ,2 ]
Pronyk, Paul [3 ,4 ,5 ]
Mohapi, Lerato
Thsabangu, Nkeko
Moshabela, Mosa [4 ,5 ]
Struthers, Helen
Gray, Glenda E.
McIntyre, James A.
Chaisson, Richard E. [1 ,2 ]
Martinson, Neil A. [1 ]
机构
[1] Johns Hopkins Univ, Sch Med, Baltimore, MD 21231 USA
[2] Johns Hopkins Univ, Bloomberg Sch Publ Hlth, Baltimore, MD USA
[3] London Sch Hyg & Trop Med, London WC1, England
[4] Univ Witwatersrand, Sch Publ Hlth, Johannesburg, South Africa
[5] Univ Witwatersrand, Perinatal HIV Res Unit, Johannesburg, South Africa
基金
美国国家卫生研究院;
关键词
HAART; isoniazid; preventive treatment; sub-Saharan Africa; tuberculosis; ACTIVE ANTIRETROVIRAL THERAPY; HUMAN-IMMUNODEFICIENCY-VIRUS; RIO-DE-JANEIRO; CONTROLLED-TRIALS; PROPHYLAXIS; IMPACT; BRAZIL;
D O I
10.1097/QAD.0b013e328327964f
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: The World Health Organization recommends isoniazid preventive therapy (IPT) for preventing tuberculosis in HIV-infected adults, although few countries have instituted this policy. Both IPT and highly active antiretroviral therapy (HAART) used separately result in reductions in tuberculosis risk. There is less information on the combined effect of IPT and HAART. We assessed the effect of IPT, HAART or both IPT and HAART on tuberculosis incidence in HIV-infected adults in South Africa. Methods: Two clinical cohorts of HIV-infected patients were studied. Primary exposures were receipt of IPT and/or HAART and the primary outcome was incident tuberculosis. Crude incident rates and incident rate ratios were calculated and Cox proportional hazards models investigated associations with tuberculosis risk. Results: Among 2778 HIV-infected patients followed for 4287 person-years, 267 incident tuberculosis cases were diagnosed [incidence rate ratio (IRR) = 6.2/100 person-years; 95% CI 5.5-7.0]. For person-time without IPT or HAART, the IRR was 7.1/100 person-years (95% CI 6.2-8.2); for person-time receiving HAART but without IPT, the IRR was 4.6/100 person-years (95% CI 3.4-6.2); for person-time after IPT but prior to HAART, the IRR was 5.2/100 person-years (95%, CI 3.4-7.8); during follow-up in patients treated with HAART after receiving IPT the IRR was 1.1/100 person-years (95% CI 0.02-7.6). Compared to treatment-naive patients, HAART-only patients had a 64% decreased hazard for tuberculosis [adjusted hazard ratio (aHR) = 0.36; 95% Cl 0.25-0.51], and patients receiving HAART after IPT had a 89% reduced hazard (aHR=0.11; 95% CI 0.02-0.78). Conclusion: Tuberculosis risk is significantly reduced by IPT in HAART-treated adults in a high-incidence operational setting in South Africa. IPT is an inexpensive and cost-effective strategy and our data strengthen calls for the implementation of IPT in conjunction with the roll-out of HAART. (c) 2009 Wolters Kluwer Health | Lippincott Williams & Wilkins
引用
收藏
页码:631 / 636
页数:6
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