Analysis of baseline laboratory characteristics of HIV-positive patients in Bulgaria treated with bictegravir /emtricitabine/ tenofovir anafelamide (early analysis)

Strashimirov Dimitar, Yordanova Ralitsa, Grozdeva Rusina, Penchev Evgeni, Ivanov Daniel, Yancheva-Petrova Nina
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Abstract

Introduction: Bictegravir/Emtricitabine/Tenofovir Anafelamide (B/F/TAF) is a recommended single tablet regimen with good tolerability and safety as well as durability of the virologic response. From its introduction in the country of Bulgaria in April 2021 till November 2021 it was given to 82 patients, followed up and treated in the Department for HIV at the Prof. Ivan Kirov Specialized Hospital for Active Treatment of Infectious and Parasitic Diseases, in 60 (72%) of which the therapeutic regimen was changed mainly from protease – inhibitor-containing regimens. Materials and methods: We present the initial 24-week period of the application of this therapeutic regimen. Our purpose was to analyze the main reasons for a switch of the cART among patients, in which the therapeutic regimen was switched, to analyse the dynamics of the basic immunologic and virologic values of the patients, and to try to analyse the safety and efficacy of the regimen. Results: Patients of nearly all age groups were enrolled in the study. The main therapeutic regimens, from which patients were switched to B/F/TAF were protease inhibitor-based, the main reason being suboptimal viral suppression, followed by simplification of cART. Side effects were the third leading cause for the switch, mainly due to gastrointestinal symptoms. Nearly half of the patients had CD 4+ T-cell count of > 500/mm3 at the time of the switch and undetectable viral load levels. The test statistical analyses of the immunological and virologic levels before and after the administration of B/F/TAF showed statistical significance as far as the viral load was concerned. Analyses of factors of prognostic importance for maintaining stable virologic response showed that CD + T-cell values, CD4:CD8 ratio before administration, VL before administration as well as time of intake proved to be of prognostic value. Cholesterol levels in patients with hypercholesterolemia were significantly lower. Conclusion: A relatively large number of patients were enrolled for a relatively short period of time; B/F/TAF proved to be of good efficacy and safety.
保加利亚接受比特拉韦/恩曲他滨/替诺福韦胺治疗的艾滋病毒阳性患者的基线实验室特征分析(早期分析)
简介Bictegravir/Emtricitabine/Tenofovir Anafelamide(B/F/TAF)是一种推荐的单片治疗方案,具有良好的耐受性和安全性,以及病毒学应答的持久性。自 2021 年 4 月引入保加利亚至 2021 年 11 月,伊万-基洛夫教授积极治疗传染病和寄生虫病专科医院艾滋病毒科对 82 名患者进行了随访和治疗,其中 60 人(72%)的治疗方案主要是从含蛋白酶抑制剂的方案转变而来。材料和方法:我们介绍了该治疗方案最初 24 周的应用情况。我们的目的是分析更换治疗方案的患者更换 cART 的主要原因,分析患者基本免疫学和病毒学数值的动态变化,并尝试分析治疗方案的安全性和有效性。研究结果几乎所有年龄段的患者都参加了这项研究。患者转用 B/F/TAF 的主要治疗方案以蛋白酶抑制剂为主,主要原因是病毒抑制效果不理想,其次是 cART 的简化。副作用是导致转药的第三大原因,主要是胃肠道症状。近一半的患者在换药时 CD 4+ T 细胞计数大于 500/mm3,病毒载量水平检测不到。对服用 B/F/TAF前后的免疫学和病毒学水平进行的测试统计分析显示,病毒载量具有统计学意义。对保持稳定病毒学应答的重要预后因素进行的分析表明,CD + T 细胞值、用药前的 CD4:CD8 比率、用药前的 VL 以及用药时间都具有预后价值。高胆固醇血症患者的胆固醇水平明显较低。结论在相对较短的时间内招募了相对较多的患者;B/F/TAF 被证明具有良好的疗效和安全性。
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