Department of Paediatrics, Harriet Shezi Children's Clinic, Faculty of Health Sciences, University of the Witwatersrand, Johannesburg, South Africa.
Pediatr Infect Dis J. 2011 Nov;30(11):974-9. doi: 10.1097/INF.0b013e31822539f6.
Antiretroviral therapy (ART) access with successful outcomes for children is expanding in resource-limited countries. The aim of this study was to determine treatment responses of children in a routine setting where first-line therapy with lopinavir/ritonavir is routinely included for young children.
Outpatient records of children who initiated ART between April 2004 and March 2008 at a government clinic in Soweto were reviewed. Children <3 years initiated ART with lopinavir/ritonavir and those ≥ 3 years initiated with efavirenz-containing regimens.
ART was initiated at a median age of 4.3 years, 28.6% also received tuberculosis treatment. During 3155 child-years of follow-up (median follow-up 17 months), 132 children (6%) died giving a mortality rate of 4.2 (95% confidence interval: 3.5, 5.0) deaths per 100 child-years. By 12 and 24 months, 84% and 96% of children achieved virologic suppression. The proportion of children with viral rebound increased from 5.4% to 16.3% at 24 and 36 months from start of ART. Younger children (receiving lopinavir/ritonavir-based first-line therapy) with higher viral loads suppressed more slowly and were more likely to die. Children who were started on treatment for tuberculosis at the time of viral suppression were more likely to have virologic rebound.
Despite good treatment outcomes overall, children with advanced disease at ART initiation had poorer outcomes, particularly those <3 years of age, most of whom were treated with lopinavir/ritonavir-containing therapy. The increasing risk of viral rebound over time for the whole cohort is concerning, given currently limited available treatment options for children.
在资源有限的国家,抗逆转录病毒疗法(ART)的应用已取得成功,为儿童带来了益处。本研究旨在确定在常规环境下的儿童治疗反应,在此环境中,洛匹那韦/利托那韦一线治疗通常适用于幼儿。
对 2004 年 4 月至 2008 年 3 月期间在索韦托的一家政府诊所接受 ART 的儿童的门诊记录进行了回顾性分析。<3 岁的儿童采用洛匹那韦/利托那韦启动 ART,≥3 岁的儿童采用含依非韦伦的方案。
ART 的中位起始年龄为 4.3 岁,28.6%的患儿同时接受结核病治疗。在 3155 儿童年的随访期间(中位随访时间为 17 个月),有 132 名儿童(6%)死亡,死亡率为每 100 儿童年 4.2(95%置信区间:3.5,5.0)例。在 12 和 24 个月时,84%和 96%的儿童达到病毒学抑制。从 ART 开始的第 24 和 36 个月,病毒反弹的儿童比例从 5.4%增加到 16.3%。病毒载量较高的年幼儿童(接受洛匹那韦/利托那韦为基础的一线治疗)抑制速度较慢,死亡风险更高。在病毒学抑制时开始治疗结核病的儿童更有可能出现病毒学反弹。
尽管总体上治疗结果良好,但在 ART 启动时患有晚期疾病的儿童预后较差,尤其是<3 岁的儿童,其中大多数接受了含洛匹那韦/利托那韦的治疗。考虑到目前儿童可用的治疗选择有限,整个队列中病毒反弹的风险随着时间的推移而增加令人担忧。