Inserm, U897 & Institut de Santé Publique, Epidémiologie et Développement (ISPED), Université Victor Segalen Bordeaux 2, Bordeaux, France.
BMC Infect Dis. 2011 Jun 23;11:182. doi: 10.1186/1471-2334-11-182.
Clinical evolution of HIV-infected children who have not yet initiated antiretroviral treatment (ART) is poorly understood in Africa. We describe severe morbidity and mortality of untreated HIV-infected children.
All HIV-infected children enrolled from 2004-2009 in a prospective HIV programme in two health facilities in Abidjan, Côte d'Ivoire, were eligible from their time of inclusion. Risks of severe morbidity (the first clinical event leading to death or hospitalisation) and mortality were documented retrospectively and estimated using cumulative incidence functions. Associations with baseline characteristics were assessed by competing risk regression models between outcomes and antiretroviral initiation.
405 children were included at a median age of 4.5 years; at baseline, 66.9% were receiving cotrimoxazole prophylaxis, and 27.7% met the 2006 WHO criteria for immunodeficiency by age. The risk of developing a severe morbid event was 14% (95%CI: 10.7 - 17.8) at 18 months; this risk was lower in children previously exposed to any prevention of mother-to-child-transmission (PMTCT) intervention (adjusted subdistribution hazard ratio [sHR]: 0.16, 95% CI: 0.04 - 0.71) versus those without known exposure. Cumulative mortality reached 5.5% (95%CI: 3.5 - 8.1) at 18 months. Mortality was associated with immunodeficiency (sHR: 6.02, 95% CI: 1.28-28.42).
Having benefited from early access to care minimizes the severe morbidity risk for children who acquire HIV. Despite the receipt of cotrimoxazole prophylaxis, the risk of severe morbidity and mortality remains high in untreated HIV-infected children. Such evidence adds arguments to promote earlier access to ART in HIV-infected children in Africa and improve care interventions in a context where treatment is still not available to all.
在非洲,尚未开始抗逆转录病毒治疗(ART)的 HIV 感染儿童的临床演变情况了解甚少。我们描述了未经治疗的 HIV 感染儿童的严重发病率和死亡率。
在科特迪瓦阿比让的两个卫生机构,2004 年至 2009 年期间,所有入组的 HIV 感染儿童都符合条件。使用累积发病率函数回顾性记录严重发病(导致死亡或住院的第一个临床事件)和死亡率,并评估其与基线特征的相关性。通过竞争风险回归模型,在结局和抗逆转录病毒治疗开始之间评估与基线特征的关联。
405 名儿童中位年龄为 4.5 岁;基线时,66.9%接受复方新诺明预防,27.7%按年龄符合 2006 年世卫组织免疫缺陷标准。18 个月时,发生严重疾病事件的风险为 14%(95%CI:10.7-17.8);与未知 PMTCT 暴露的儿童相比,之前接受任何 PMTCT 干预的儿童(调整后的亚分布危险比[sHR]:0.16,95%CI:0.04-0.71)风险较低。18 个月时,累积死亡率达到 5.5%(95%CI:3.5-8.1)。死亡率与免疫缺陷有关(sHR:6.02,95%CI:1.28-28.42)。
早期获得治疗可最大程度降低获得 HIV 的儿童的严重发病风险。尽管接受了复方新诺明预防,未经治疗的 HIV 感染儿童仍存在严重发病和死亡的高风险。此类证据为在非洲促进 HIV 感染儿童更早获得 ART 提供了依据,并在尚未为所有人提供治疗的情况下,改善了治疗干预措施。