Cause-Specific Mortality and the Contribution of Immune Reconstitution Inflammatory Syndrome in the First 3 Years after Antiretroviral Therapy Initiation in an Urban African Cohort

被引:107
作者
Castelnuovo, Barbara [1 ]
Manabe, Yukari C. [1 ,3 ]
Kiragga, Agnes [1 ]
Kamya, Moses [2 ]
Easterbrook, Philippa [4 ]
Kambugu, Andrew [1 ]
机构
[1] Makerere Univ, Infect Dis Inst, Kampala, Uganda
[2] Makerere Univ, Dept Med, Kampala, Uganda
[3] Johns Hopkins Univ, Sch Med, Div Infect Dis, Dept Med, Baltimore, MD 21205 USA
[4] Kings Coll London, London WC2R 2LS, England
基金
英国医学研究理事会;
关键词
HIV-INFECTED PATIENTS; SUB-SAHARAN AFRICA; SOUTH-AFRICA; RISK-FACTORS; CRYPTOCOCCAL ANTIGENEMIA; HIV-1-INFECTED ADULTS; TREATMENT PROGRAM; SCALE-UP; TUBERCULOSIS; SURVIVAL;
D O I
10.1086/605500
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. Although many studies have reported high early mortality among patients enrolled in antiretroviral therapy (ART) programs in sub-Saharan Africa-particularly among those individuals with advanced immunodeficiency -few studies have reported the most common causes of these early deaths Methods. We determined cause-specific mortality and the contribution of immune reconstitution inflammatory syndrome (IRIS) in a well-characterized patient cohort in Kampala, Uganda, over a 36-month period of ART. Results. In a cohort of patients who initiated antiretroviral therapy in Uganda, we observed a high early mortality rate among patients with advanced disease. The most common causes of death were tuberculosis and cryptococcal meningitis. The contribution of immune reconstitution inflammatory syndrome to mortality was limited. Conclusions. We show a significant early mortality in our ART cohort in resource-limited settings that is driven by advanced human immunodeficiency virus disease and characterized by low CD4 cell counts. In our experience, the contribution of IRIS to this observed early mortality is limited.
引用
收藏
页码:965 / 972
页数:8
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