Schomaker Michael, Davies Mary-Ann, Malateste Karen, Renner Lorna, Sawry Shobna, N'Gbeche Sylvie, Technau Karl-Günter, Eboua François, Tanser Frank, Sygnaté-Sy Haby, Phiri Sam, Amorissani-Folquet Madeleine, Cox Vivian, Koueta Fla, Chimbete Cleophas, Lawson-Evi Annette, Giddy Janet, Amani-Bosse Clarisse, Wood Robin, Egger Matthias, Leroy Valeriane
From the aCentre for Infectious Disease Epidemiology and Research, University of Cape Town, Cape Town, South Africa; bInstitute of Epidemiology and Public Health, University of Bordeaux, Bordeaux, France; cUniversity of Ghana Medical School, Accra, Ghana; dWits Reproductive Health and HIV Institute, Harriet Shezi Children's Clinic, Chris Hani Baragwanath Academic Hospital, University of the Witwatersrand, Soweto, South Africa; eCentre de Prise en Charge de Recherche et de Formation Enfants, Abidjan, Côte d'Ivoire; fEmpilweni Service and Research Unit, Rahima Moosa Mother and Child Hospital and University of the Witwatersrand, Johannesburg, South Africa; gYopougon University Hospital, Abidjan, Côte d'Ivoire; hAfrica Centre for Health and Population Studies, University of KwaZulu-Natal, Somkhele, South Africa; iAlbert Royer Hospital, Dakar, Senegal; jLighthouse Trust Clinic, Kamuzu Central Hospital, Lilongwe, Malawi; kUniversity of North Carolina, Chapel Hill, NC; lFélix Houphouët Boigny University Hospital, Abidjan, Côte d'Ivoire; mMédecins Sans Frontiéres South Africa, CapeTown, South Africa; nKhayelitsha ART Programme, Khayelitsha, Cape Town, South Africa; oCharles de Gaulle University Hospital, Ouagadougou, Burkina Faso; pNewlands Clinic, Harare, Zimbabwe; qHospital du Tokoin, Lomé, Togo; rSinikithemba Clinic, McCord Hospital, Durban, South Africa; sMTCT-Plus Center, Abidjan, Côte d'Ivoire; tDesmond Tutu HIV Centre, Cape Town, South Africa; uInstitute of Infectious Diseases and Molecular Medicine, University of Cape Town, Cape Town, South Africa; vInstitute of Social and Preventive Medicine, University of Bern, Bern, Switzerland; and wInserm, U897, Epidémiologie-Biostatistiques, Université Bordeaux, Bordeaux, France.
Epidemiology. 2016 Mar;27(2):237-46. doi: 10.1097/EDE.0000000000000412.
There is limited evidence regarding the optimal timing of initiating antiretroviral therapy (ART) in children. We conducted a causal modeling analysis in children ages 1-5 years from the International Epidemiologic Databases to Evaluate AIDS West/Southern-Africa collaboration to determine growth and mortality differences related to different CD4-based treatment initiation criteria, age groups, and regions.
ART-naïve children of ages 12-59 months at enrollment with at least one visit before ART initiation and one follow-up visit were included. We estimated 3-year growth and cumulative mortality from the start of follow-up for different CD4 criteria using g-computation.
About one quarter of the 5,826 included children was from West Africa (24.6%).The median (first; third quartile) CD4% at the first visit was 16% (11%; 23%), the median weight-for-age z-scores and height-for-age z-scores were -1.5 (-2.7; -0.6) and -2.5 (-3.5; -1.5), respectively. Estimated cumulative mortality was higher overall, and growth was slower, when initiating ART at lower CD4 thresholds. After 3 years of follow-up, the estimated mortality difference between starting ART routinely irrespective of CD4 count and starting ART if either CD4 count <750 cells/mm³ or CD4% <25% was 0.2% (95% CI = -0.2%; 0.3%), and the difference in the mean height-for-age z-scores of those who survived was -0.02 (95% CI = -0.04; 0.01). Younger children ages 1-2 and children in West Africa had worse outcomes.
Our results demonstrate that earlier treatment initiation yields overall better growth and mortality outcomes, although we could not show any differences in outcomes between immediate ART and delaying until CD4 count/% falls below 750/25%.
关于儿童开始抗逆转录病毒治疗(ART)的最佳时机,证据有限。我们对来自国际流行病学数据库以评估艾滋病西/南部非洲合作项目中1至5岁的儿童进行了因果模型分析,以确定与基于不同CD4的治疗起始标准、年龄组和地区相关的生长和死亡率差异。
纳入了入组时年龄为12至59个月、在开始ART前至少有一次就诊且有一次随访就诊的未接受过ART的儿童。我们使用g计算法从随访开始时估计不同CD4标准下的3年生长情况和累积死亡率。
纳入的5826名儿童中约四分之一来自西非(24.6%)。首次就诊时CD4%的中位数(第一四分位数;第三四分位数)为16%(11%;23%),年龄别体重z评分和年龄别身高z评分的中位数分别为-1.5(-2.7;-0.6)和-2.5(-3.5;-1.5)。当在较低的CD4阈值开始ART时,总体估计累积死亡率较高,生长较慢。随访3年后,无论CD4计数如何常规开始ART与当CD4计数<750个细胞/mm³或CD4%<25%时开始ART之间的估计死亡率差异为0.2%(95%CI=-0.2%;0.3%),存活者的年龄别身高z评分均值差异为-0.02(95%CI=-0.04;0.01)。1至2岁的幼儿和西非的儿童预后较差。
我们的结果表明,更早开始治疗总体上能产生更好的生长和死亡率结果,尽管我们未能显示立即开始ART与延迟至CD4计数/%降至750/25%以下之间在结果上有任何差异。