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在南非开始抗逆转录病毒治疗的HIV-1感染儿童的预后:治疗项目的合作分析

Prognosis of children with HIV-1 infection starting antiretroviral therapy in Southern Africa: a collaborative analysis of treatment programs.

作者信息

Davies Mary-Ann, May Margaret, Bolton-Moore Carolyn, Chimbetete Cleophas, Eley Brian, Garone Daniela, Giddy Janet, Moultrie Harry, Ndirangu James, Phiri Sam, Rabie Helena, Technau Karl-Günter, Wood Robin, Boulle Andrew, Egger Matthias, Keiser Olivia

机构信息

From the *School of Public Health and Family Medicine, University of Cape Town, Cape Town, South Africa; †School of Social and Community Medicine, University of Bristol, Bristol, United Kingdom; ‡Centre for Infectious Disease Research in Zambia, Lusaka, Zambia; §University of North Carolina, Chapel Hill, NC; ¶Newlands clinic, Harare, Zimbabwe; ‖Red Cross Children's Hospital and School of Child and Adolescent Health, University of Cape Town; **Médecins Sans Frontières (MSF) South Africa and Khayelitsha ART Programme, Cape Town; ††Sinikithemba Clinic, McCord Hospital, Durban; ‡‡Wits Reproductive Health and HIV Institute, University of the Witwatersrand, Johannesburg; §§Harriet Shezi Children's Clinic, Chris Hani Baragwanath Hospital, Soweto; ¶¶Africa Centre for Health and Population Studies, University of Kwazulu-Natal, Somkhele, South Africa; ‖‖Lighthouse Trust Clinic, Kamuzu Central Hospital, Lilongwe, Malawi and Liverpool School of Tropical Medicine, Liverpool, United Kingdom; ***Tygerberg Academic Hospital, University of Stellenbosch, Stellenbosch; †††Empilweni Services and Research Unit, Rahima Moosa Mother and Child Hospital, and University of the Witwatersrand, Johannesburg; ‡‡‡Gugulethu ART Programme and Desmond Tutu HIV Centre, University of Cape Town, Cape Town, South Africa; and §§§Institute of Social and Preventive Medicine (ISPM), University of Bern, Switzerland.

出版信息

Pediatr Infect Dis J. 2014 Jun;33(6):608-16. doi: 10.1097/INF.0000000000000214.

Abstract

BACKGROUND

Prognostic models for children starting antiretroviral therapy (ART) in Africa are lacking. We developed models to estimate the probability of death during the first year receiving ART in Southern Africa.

METHODS

We analyzed data from children ≤10 years of age who started ART in Malawi, South Africa, Zambia or Zimbabwe from 2004 to 2010. Children lost to follow up or transferred were excluded. The primary outcome was all-cause mortality in the first year of ART. We used Weibull survival models to construct 2 prognostic models: 1 with CD4%, age, World Health Organization clinical stage, weight-for-age z-score (WAZ) and anemia and the other without CD4%, because it is not routinely measured in many programs. We used multiple imputation to account for missing data.

RESULTS

Among 12,655 children, 877 (6.9%) died in the first year of ART. We excluded 1780 children who were lost to follow up/transferred from main analyses; 10,875 children were therefore included. With the CD4% model probability of death at 1 year ranged from 1.8% [95% confidence interval (CI): 1.5-2.3] in children 5-10 years with CD4% ≥10%, World Health Organization stage I/II, WAZ ≥ -2 and without severe anemia to 46.3% (95% CI: 38.2-55.2) in children <1 year with CD4% < 5%, stage III/IV, WAZ< -3 and severe anemia. The corresponding range for the model without CD4% was 2.2% (95% CI: 1.8-2.7) to 33.4% (95% CI: 28.2-39.3). Agreement between predicted and observed mortality was good (C-statistics = 0.753 and 0.745 for models with and without CD4%, respectively).

CONCLUSIONS

These models may be useful to counsel children/caregivers, for program planning and to assess program outcomes after allowing for differences in patient disease severity characteristics.

摘要

背景

非洲缺乏针对开始抗逆转录病毒治疗(ART)的儿童的预后模型。我们开发了模型来估计南部非洲接受ART的第一年期间的死亡概率。

方法

我们分析了2004年至2010年在马拉维、南非、赞比亚或津巴布韦开始接受ART的10岁及以下儿童的数据。失访或转院的儿童被排除。主要结局是ART第一年的全因死亡率。我们使用威布尔生存模型构建了2个预后模型:1个模型纳入了CD4%、年龄、世界卫生组织临床分期、年龄别体重Z评分(WAZ)和贫血情况,另一个模型未纳入CD4%,因为许多项目中未常规测量该指标。我们使用多重填补法处理缺失数据。

结果

在12,655名儿童中,877名(6.9%)在ART的第一年死亡。我们将1780名失访/转院的儿童排除在主要分析之外;因此纳入分析的儿童有10,875名。对于包含CD4%的模型,1岁时的死亡概率在5至10岁、CD4%≥10%、世界卫生组织I/II期、WAZ≥ -2且无重度贫血的儿童中为1.8%[95%置信区间(CI):1.5 - 2.3],在年龄<1岁、CD4%<5%、III/IV期、WAZ< -3且有重度贫血的儿童中为46.3%(95%CI:38.2 - 55.2)。不包含CD4%的模型的相应范围为2.2%(95%CI:1.8 - 2.7)至33.4%(95%CI:28.2 - 39.3)。预测死亡率与观察到的死亡率之间的一致性良好(包含CD4%和不包含CD4%的模型的C统计量分别为0.753和0.745)。

结论

在考虑患者疾病严重程度特征差异后,这些模型可能有助于为儿童/照顾者提供咨询、进行项目规划以及评估项目结果。

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