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Viral load versus CD4⁺ monitoring and 5-year outcomes of antiretroviral therapy in HIV-positive children in Southern Africa: a cohort-based modelling study.

机译:南部非洲HIV阳性儿童的病毒载量与CD4⁺监​​测以及抗逆转录病毒疗法的5年结局:基于队列的模型研究。

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摘要

OBJECTIVESududMany paediatric antiretroviral therapy (ART) programmes in Southern Africa rely on CD4⁺ to monitor ART. We assessed the benefit of replacing CD4⁺ by viral load monitoring.ududDESIGNududA mathematical modelling study.ududMETHODSududA simulation model of HIV progression over 5 years in children on ART, parameterized by data from seven South African cohorts. We simulated treatment programmes with 6-monthly CD4⁺ or 6- or 12-monthly viral load monitoring. We compared mortality, second-line ART use, immunological failure and time spent on failing ART. In further analyses, we varied the rate of virological failure, and assumed that the rate is higher with CD4⁺ than with viral load monitoring.ududRESULTSududAbout 7% of children were predicted to die within 5 years, independent of the monitoring strategy. Compared with CD4⁺ monitoring, 12-monthly viral load monitoring reduced the 5-year risk of immunological failure from 1.6 to 1.0% and the mean time spent on failing ART from 6.6 to 3.6 months; 1% of children with CD4⁺ compared with 12% with viral load monitoring switched to second-line ART. Differences became larger when assuming higher rates of virological failure. When assuming higher virological failure rates with CD4⁺ than with viral load monitoring, up to 4.2% of children with CD4⁺ compared with 1.5% with viral load monitoring experienced immunological failure; the mean time spent on failing ART was 27.3 months with CD4⁺ monitoring and 6.0 months with viral load monitoring. Conclusion: Viral load monitoring did not affect 5-year mortality, but reduced time on failing ART, improved immunological response and increased switching to second-line ART.
机译:目标 ud ud南部非洲的许多儿科抗逆转录病毒疗法(ART)计划都依靠CD4⁺来监测ART。我们评估了通过病毒载量监测来替代CD4 the的益处。 ud udDESIGN ud ud数学建模研究。 ud udMETHODS ud udA儿童5年以上艾滋病毒进展的模拟模型,参数来自七个南非队列。我们模拟了每月6次CD4⁺或6个月或12个月病毒载量监测的治疗方案。我们比较了死亡率,二线抗逆转录病毒疗法的使用,免疫功能衰竭和失败的时间。在进一步的分析中,我们改变了病毒学失败的发生率,并假设CD4⁺的发生率高于病毒载量监测。 ud udRESULTS ud ud预计约有7%的儿童在5年内死亡,与监控策略。与CD4⁺监​​测相比,每12个月一次病毒载量监测将5年免疫功能衰竭的风险从1.6%降低到1.0%,平均ART失败时间从6.6个月降低到3.6个月; 1%的CD4⁺儿童与12%的病毒载量监测改为二线抗逆转录病毒疗法。当假设病毒学失败率更高时,差异会更大。当假定CD4⁺的病毒学失败率高于病毒载量监测时,高达4.2%的CD4⁺儿童发生免疫学失败的比例为1.5%,而病毒载量监测则为1.5%。通过CD4⁺监​​测,ART失败的平均时间为27.3个月,通过病毒载量监测为6.0个月。结论:病毒载量监测并没有影响5年死亡率,但减少了ART失败的时间,改善了免疫反应,并增加了向二线ART的转换。

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