感染艾滋病毒的儿童和青少年抗逆转录病毒治疗的病毒学失败及相关的社会和临床因素

A. Y. Sambyalova, T. Bairova, T. L. Manaenkova, A. Belskikh, Y. Plotnikova, L. V. Rychkov
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引用次数: 0

摘要

根据世界卫生组织,在感染艾滋病毒/艾滋病的儿童和青少年中,应实现90%的持续病毒学抑制,这使得评估抗逆转录病毒治疗的病毒学失败的流行情况变得重要。本研究的目的是确定病毒学失败的患病率和与之相关的临床因素,以及按病毒载量水平分组的儿童和青少年艾滋病毒感染者的治疗药物监测。材料和方法:对184名接受抗逆转录病毒治疗并在伊尔库茨克预防和控制艾滋病和传染病区域中心登记的儿童和青少年的医疗记录进行了回顾性分析。该研究包括172名1-18岁的围产期艾滋病毒感染儿童。根据病毒载量水平将患者分为3组:1 ~ 21例患者病毒载量> 1000拷贝/ml血浆,2 ~ 42例患者病毒载量50 ~ 1000拷贝/ml血浆,3 ~ 109例患者病毒载量检测不到(< 50拷贝/ml)。所有患者都按照治疗儿童艾滋病毒感染的临床指南进行了标准检测,并进行了治疗性药物监测。结果。在持续抗逆转录病毒治疗的背景下,大量患者21 / 172(12.2%)出现病毒学失败。不完全抑制HIV复制的儿童和青少年比例为42 / 172(24.4%)。通过改变ART治疗方案,差异有统计学意义(p = 0.031)。在第一组中,改变治疗方案的患者比例为7 / 21(33.3%),比零病毒载量组的70 / 109(64.2%)少2倍。在三个对照组中,利托那韦和洛匹那韦零浓度的儿童和青少年比例存在差异(p = 0,020和p = 0,012)。利托那韦零浓度患者分布如下:第一组为3 / 17(17.6%),第二组为8/37(21.6%),第三组为4/80 (5%);洛匹那韦分别为4/17(23.5%)、6/36(16.7%)、3/80(3.8%)。结论。这项研究表明,在接受抗逆转录病毒治疗的儿童和青少年中,病毒学失败的发生率仍然很高。为了在服用蛋白酶抑制剂方案的儿童和青少年中实现持续的病毒学抑制,必须增加对治疗的依从性。治疗药物监测可以作为评估依从性的方法之一。
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Virological failure of antiretroviral therapy and associated social and clinical factors in children and adolescents living with HIV
   According to the World Health Organization, sustained virological suppression of 90 % should be achieved among children and adolescents living with HIV / AIDS, which makes it important to assess the prevalence of virological failure of antiretroviral therapy.   The aim of this study was to determine the prevalence of virological failure and the clinical factors associated with it, as well as therapeutic drug monitoring in groups divided by the viral load level among children and adolescents with HIV.   Materials and Methods: A retrospective analysis of the medical records of 184 children and adolescents receiving antiretroviral therapy and registered at the Irkutsk Regional Center for the Prevention and Control of AIDS and Infectious Diseases, Irkutsk, was carried out. The study included 172 children aged 1-18 years with perinatal HIV infection. Patients were divided into groups depending on the level of viral load: group 1 – 21 patients with viral load > 1000 copies/ml of plasma, group 2 – 42 patients with viral load 50– 1000 copies/ml of plasma, group 3 – 109 patients with undetectable viral load (< 50 copies/ml). All patients underwent standard tests in accordance with clinical guidelines for the treatment of HIV infection in children, as well as therapeutic drug monitoring.   Results. Against the background of ongoing antiretroviral therapy, a significant number of patients 21 / 172 (12,2 %) experienced virological failure. The proportion of children and adolescents with incomplete suppression of HIV replication is 42 / 172 (24,4 %). Statistically significant differences were obtained by changing the ART regimen (p = 0,031). In the first group, the proportion of patients who changed the therapy regimen is 7 / 21 (33,3 %), which is two times less than in the group with a zero viral load of 70 / 109 (64,2 %). There are differences in the proportion of children and adolescents with zero concentrations of ritonavir and lopinavir (p = 0,020 and p = 0,012) in the three compared groups. The distribution of patients with zero concentrations was as follows: for ritonavir in the first group 3 / 17 (17,6 %), in the second – 8/37 (21,6 %), in the third group – 4/80 (5 %); for lopinavir – 4/17 (23,5 %), 6/36 (16,7 %), 3/80 (3,8 %), respectively.   Conclusion. This study demonstrates that the prevalence of virological failure among children and adolescents receiving ART remains high. To achieve sustained virological suppression in children and adolescents taking a protease inhibitor regimen, adherence to therapy must be increased. As one of the methods for assessing adherence, therapeutic drug monitoring can be used.
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