Outcome of HIV-associated tuberculosis in the era of highly active antiretroviral therapy

被引:153
|
作者
Dheda, K [1 ]
Lampe, FC
Johnson, MA
Lipman, MC
机构
[1] Royal Free & UCL, Sch Med, Dept HIV & Thorac Med, London NW3 2QG, England
[2] Royal Free & UCL, Sch Med, Dept Primary Care & Populat Sci, London NW3 2QG, England
来源
JOURNAL OF INFECTIOUS DISEASES | 2004年 / 190卷 / 09期
关键词
D O I
10.1086/424676
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 benefit of highly active antiretroviral therapy (HAART) in the treatment of patients coinfected with tuberculosis ( TB) and human immunodeficiency virus (HIV) is unclear because of concerns about treatment-related complications. Methods. We compared outcomes in patients starting TB treatment during the pre-HAART era ( before 1996; n = 36) with those in patients starting treatment during the HAART era ( during or after 1996;). Results. During a median of 3.6 years of follow-up, 49 patients died or had an AIDS event. Compared with patients in the pre-HAART group, those in the HAART group had a lower risk of death ( cumulative at 4 years, 43% vs. 22%; P = .012) and of death or having an AIDS event (69% vs. 43%; P = .023). Event risk within the Pp. 012 Pp. 023 first 2 months of TB treatment was exceptionally high in patients with CD4(+) cell counts <100 cells/mm(3) and declined thereafter. HAART use during follow-up was associated with a marked reduction in event risk ( adjusted hazard ratio, 0.38 [95% confidence interval, 0.16 - 0.91]). Conclusions. HAART substantially reduces new AIDS events and death in coinfected patients. Those with a CD4(+) cell count <100 cells/mm(3) have a high event risk during the intensive phase of anti-TB treatment. These data should be taken into account when deciding to delay HAART in coinfected patients with CD4(+) cell counts < 100 cells/mm(3).
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收藏
页码:1670 / 1676
页数:7
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