Optimum time to start antiretroviral therapy during HIV-associated opportunistic infections

被引:43
作者
Lawn, Stephen D. [1 ,2 ]
Toeroek, M. Estee [3 ]
Wood, Robin [1 ]
机构
[1] Univ Cape Town, Fac Hlth Sci, Inst Infect Dis & Mol Med, Desmond Tutu HIV Ctr, ZA-7925 Cape Town, South Africa
[2] London Sch Hyg & Trop Med, Dept Infect & Trop Dis, Clin Res Unit, London WC1, England
[3] Cambridge Univ Hosp NHS Fdn Trust, Dept Infect Dis, Cambridge, England
基金
英国惠康基金; 美国国家卫生研究院;
关键词
antiretroviral; HIV; opportunistic infection; timing; when to start; RECONSTITUTION INFLAMMATORY SYNDROME; SUB-SAHARAN AFRICA; HIGH-INCOME COUNTRIES; EARLY MORTALITY; SOUTH-AFRICA; HIV-1-INFECTED PATIENTS; COLLABORATIVE ANALYSIS; VIROLOGICAL RESPONSE; TUBERCULOSIS THERAPY; TREATMENT OUTCOMES;
D O I
10.1097/QCO.0b013e3283420f76
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Purpose of review We review recently published literature concerning the optimum time to start antiretroviral therapy (ART) in patients with HIV-associated opportunistic infections. Recent findings In addition to data from observational studies, results from six randomized controlled clinical trials were available by July 2010. The collective findings of these trials were that patients with CD4 cell counts less than 200 cells/mu l who start ART within the first 2 weeks of treatment for opportunistic infections including Pneumocystis jirovecii pneumonia, serious bacterial infections or pulmonary tuberculosis have lower mortality when compared to patients starting ART at later time-points. Moreover, patients with pulmonary tuberculosis and CD4 counts of 200-500 cells/mu l who started ART during tuberculosis (TB) treatment had improved survival compared to those who deferred ART until after the end of treatment. In contrast, in two separate studies, immediate ART conferred no survival benefit in patients with TB meningitis and was associated with substantially higher mortality risk in patients with cryptococcal meningitis. Summary Initiation of ART during the first 2 weeks of treatment for serious opportunistic infections has been shown to be associated with improved survival with the exception of patients with tuberculous meningitis and cryptococcal meningitis. Further clinical trials are ongoing.
引用
收藏
页码:34 / 42
页数:9
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