Birhan Tilahun Yemanu, Gezie Lemma Derseh, Teshome Destaw Fetene, Sisay Malede Mequanent
Department of Epidemiology and Biostatistics, Institute of Public Health, College of Medicine & Health Sciences, University of Gondar, Gondar, Ethiopia.
Trop Med Health. 2020 May 22;48:37. doi: 10.1186/s41182-020-00224-9. eCollection 2020.
Human immunodeficiency virus (HIV) infection results in a gradual depletion of immune function, particularly CD4 cells. The CD4 assessment plays a significant role in assessing treatment responses and clinical decision-making for patients on combination antiretroviral therapy (ART) in resource-limited settings. However, new data on CD4 count changes are scarce; the volatility of CD4 counts after initiation of ART over time remains largely uncharacterized. This study aimed to identify the predictors of CD4 changes over time among HIV-infected children who began ART in Amhara, Ethiopia.
A retrospective follow-up study was performed. A total of 983 HIV-infected children who initiated ART in government hospitals in the Amhara region between 2010 and 2016 were included using a simple random sampling technique. Data were extracted using a structured checklist. An exploratory data analysis was carried out to explain individual and average profile plots. The linear mixed model was used to identify the CD4 change count predictors over time. Variables with value < 0.05 were considered statistically significant in a multivariable linear mixed regression analysis.
The mean CD4 count of the participants was 465.1 cells/mm with an average CD4 count increase of 30.06 cells/mm over 6 months from baseline CD4 count and ART initiation. Childhood age ( = - 0.015; 95% Cl - 0.021, - 0.009), opportunistic infection at ART initiation ( = - 0.044, 95% CI - 0.085, - 0.004), hemoglobin level ( = 0.013; 95% CI 0.004, 0.022), and baseline WHO clinical stage II ( = - 0.046, 95% CI - 0.091, - 0.0003) were significant predictors of CD4 changes over time.
The average CD4 count increase was sufficient in HIV patients who began combined antiretroviral therapy over time. The younger age of the infant, the higher baseline level of hemoglobin, the baseline WHO clinical stage II, and opportunistic infections led to changes in CD4 counts. As a result, timely diagnosis and treatment of opportunistic infections will reduce the risk of opportunistic infections.
人类免疫缺陷病毒(HIV)感染会导致免疫功能逐渐耗竭,尤其是CD4细胞。在资源有限的环境中,CD4评估对于评估接受联合抗逆转录病毒疗法(ART)的患者的治疗反应和临床决策具有重要作用。然而,关于CD4计数变化的新数据很少;ART开始后CD4计数随时间的波动情况在很大程度上仍未得到描述。本研究旨在确定在埃塞俄比亚阿姆哈拉地区开始接受ART的HIV感染儿童中,CD4随时间变化的预测因素。
进行了一项回顾性随访研究。采用简单随机抽样技术,纳入了2010年至2016年期间在阿姆哈拉地区政府医院开始接受ART的983名HIV感染儿童。使用结构化检查表提取数据。进行探索性数据分析以解释个体和平均概况图。使用线性混合模型确定CD4随时间变化计数的预测因素。在多变量线性混合回归分析中,P值<0.05的变量被认为具有统计学意义。
参与者的平均CD4计数为465.1个细胞/mm³,从基线CD4计数和开始接受ART起的6个月内,平均CD4计数增加了30.06个细胞/mm³。儿童年龄(P = -0.015;95%置信区间 -0.021,-0.009)、开始接受ART时的机会性感染(P = -0.044,95%置信区间 -0.085,-0.004)、血红蛋白水平(P = 0.013;95%置信区间 0.004,0.022)以及基线WHO临床分期II(P = -0.046,95%置信区间 -0.091,-0.0003)是CD4随时间变化的显著预测因素。
随着时间推移,开始接受联合抗逆转录病毒疗法的HIV患者的平均CD4计数增加是足够的。婴儿年龄越小、血红蛋白基线水平越高、基线WHO临床分期II以及机会性感染会导致CD4计数发生变化。因此,及时诊断和治疗机会性感染将降低机会性感染的风险。