Prognosis of patients with HIV-1 infection starting antiretroviral therapy in sub-Saharan Africa: a collaborative analysis of scale-up programmes

被引:190
作者
May, Margaret [2 ]
Boulle, Andrew [3 ]
Phiri, Sam [6 ]
Messou, Eugene [7 ,8 ]
Myer, Landon [3 ,4 ,5 ]
Wood, Robin [9 ]
Keiser, Olivia [1 ]
Sterne, Jonathan A. C. [2 ]
Dabis, Francois [10 ]
Egger, Matthias [1 ]
机构
[1] Univ Bern, Inst Social & Prevent Med, CH-3012 Bern, Switzerland
[2] Univ Bristol, Dept Social Med, Bristol, Avon, England
[3] Univ Cape Town, Sch Publ Hlth & Family Med, Ctr Infect Dis Epidemiol & Res, ZA-7925 Cape Town, South Africa
[4] Columbia Univ, Int Ctr AIDS Care & Treatment Programs, New York, NY USA
[5] Columbia Univ, Mailman Sch Publ Hlth, Dept Epidemiol, New York, NY USA
[6] Lighthouse Trust Kamuzu Cent Hosp, Lilongwe, Malawi
[7] CEPREF Clin, Abidjan, Cote Ivoire
[8] Programme PAC CI, Abidjan, Cote Ivoire
[9] Univ Cape Town, Fac Hlth Sci, Inst Infect Dis & Mol Med, Desmond Tutu HIV Ctr, ZA-7925 Cape Town, South Africa
[10] Univ Victor Segalen, ISPED, INSERM, U897, Bordeaux, France
基金
瑞士国家科学基金会; 美国国家卫生研究院; 英国医学研究理事会;
关键词
HIV-1-INFECTED PATIENTS; POSITIVE PATIENTS; SURVIVAL; ANEMIA; MORTALITY; ADULTS; SETTINGS; GENDER; MODEL; ERA;
D O I
10.1016/S0140-6736(10)60666-6
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background Prognostic models have been developed for patients infected with HIV-1 who start combination antiretroviral therapy (ART) in high-income countries, but not for patients in sub-Saharan Africa. We developed two prognostic models to estimate the probability of death in patients starting ART in sub-Saharan Africa. Methods We analysed data for adult patients who started ART in four scale-up programmes in Cote d'Ivoire, South Africa, and Malawi from 2004 to 2007. Patients lost to follow-up in the first year were excluded. We used Weibull survival models to construct two prognostic models: one with CD4 cell count, clinical stage, bodyweight, age, and sex (CD4 count model); and one that replaced CD4 cell count with total lymphocyte count and severity of anaemia (total lymphocyte and haemoglobin model), because CD4 cell count is not routinely measured in many African ART programmes. Death from all causes in the first year of ART was the primary outcome. Findings 912 (8.2%) of 11 153 patients died in the first year of ART. 822 patients were lost to follow-up and not included in the main analysis; 10331 patients were analysed. Mortality was strongly associated with high baseline CD4 cell count (>= 200 cells per mu L vs <25; adjusted hazard ratio 0.21, 95% CI 0.17-0.27), WHO clinical stage (stages III-IV vs I-II; 3.45, 2.43-4.90), bodyweight (60 kg vs <45 kg; 0.23, 0.18-0.30), and anaemia status (none vs severe: 0.27, 0.20-0.36). Other independent risk factors for mortality were low total lymphocyte count, advanced age, and male sex. Probability of death at 1 year ranged from 0.9% (95% CI 0.6-1.4) to 52.5% (43.8-61.7) with the CD4 model, and from 0.9% (0.5-1.4) to 59.6% (48.2-71.4) with the total lymphocyte and haemoglobin model. Both models accurately predict early mortality in patients starting ART in sub-Saharan Africa compared with observed data. Interpretation Prognostic models should be used to counsel patients, plan health services, and predict outcomes for patients with HIV-1 infection in sub-Saharan Africa.
引用
收藏
页码:449 / 457
页数:9
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