HIV Center, National Institute of Hematology and Infectious Diseases, South Pest Central Hospital, Budapest, Hungary.
Department of Adults' Infectious Diseases, Hospital for Infectious Diseases, Medical University of Warsaw, Warsaw, Poland.
HIV Med. 2022 Jul;23(6):693-700. doi: 10.1111/hiv.13214. Epub 2021 Dec 3.
The aim of this international multicentre study was to review potential drug-drug interactions (DDIs) for real-life coadministration of combination antiretroviral therapy (cART) and coronavirus disease 2019 (COVID-19)-specific medications.
The Euroguidelines in Central and Eastern Europe Network Group initiated a retrospective, observational cohort study of HIV-positive patients diagnosed with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection. Data were collected through a standardized questionnaire and DDIs were identified using the University of Liverpool's interaction checker.
In total, 524 (94.1% of 557) patients received cART at COVID-19 onset: 117 (22.3%) were female, and the median age was 42 (interquartile range 36-50) years. Only 115 (21.9%) patients were hospitalized, of whom 34 required oxygen therapy. The most frequent nucleoside reverse transcriptase inhibitor (NRTI) backbone was tenofovir disoproxil fumarate (TDF)/tenofovir alafenamide (TAF) with lamivudine or emtricitabine (XTC) (79.3%) along with an integrase strand transfer inhibitor (INSTI) (68.5%), nonnucleoside reverse transcriptase inhibitor (NNRTI) (17.7%), protease inhibitor (PI) (13.7%) or other (2.5%). In total, 148 (28.2%) patients received COVID-19-specific treatments: corticosteroids (15.7%), favipiravir (7.1%), remdesivir (3.1%), hydroxychloroquine (2.7%), tocilizumab (0.6%) and anakinra (0.2%). In total, 62 DDI episodes were identified in 58 patients (11.8% of the total cohort and 41.9% of the COVID-19-specific treatment group). The use of boosted PIs and elvitegravir accounted for 43 DDIs (29%), whereas NNRTIs were responsible for 14 DDIs (9.5%).
In this analysis from the Central and Eastern European region on HIV-positive persons receiving COVID-19-specific treatment, it was found that potential DDIs were common. Although low-dose steroids are mainly used for COVID-19 treatment, comedication with boosted antiretrovirals seems to have the most frequent potential for DDIs. In addition, attention should be paid to NNRTI coadministration.
本国际多中心研究旨在回顾在联合使用抗逆转录病毒疗法(cART)和新型冠状病毒病(COVID-19)特异性药物的真实情况下,潜在的药物相互作用(DDI)。
东欧和中欧 Euroguidelines 指南网络组启动了一项回顾性观察队列研究,纳入了诊断为严重急性呼吸综合征冠状病毒 2(SARS-CoV-2)感染的 HIV 阳性患者。通过标准化问卷收集数据,并使用利物浦大学的相互作用检查器识别 DDI。
共 524 例(557 例的 94.1%)患者在 COVID-19 发病时接受 cART:117 例(22.3%)为女性,中位年龄为 42(四分位间距 36-50)岁。仅有 115 例(21.9%)患者住院,其中 34 例需要氧疗。最常见的核苷逆转录酶抑制剂(NRTI)骨干是替诺福韦二吡呋酯(TDF)/替诺福韦艾拉酚胺(TAF)联合拉米夫定或恩曲他滨(XTC)(79.3%),同时联合整合酶链转移抑制剂(INSTI)(68.5%)、非核苷逆转录酶抑制剂(NNRTI)(17.7%)、蛋白酶抑制剂(PI)(13.7%)或其他(2.5%)。共有 148 例(28.2%)患者接受 COVID-19 特异性治疗:皮质类固醇(15.7%)、法匹拉韦(7.1%)、瑞德西韦(3.1%)、羟氯喹(2.7%)、托珠单抗(0.6%)和阿那白滞素(0.2%)。共发现 58 例患者(总队列的 11.8%和 COVID-19 特异性治疗组的 41.9%)发生 62 例 DDI 事件。使用增效型 PI 和艾维雷韦导致 43 例 DDI(29%),而 NNRTI 导致 14 例 DDI(9.5%)。
在这项来自东欧和中欧地区的 HIV 阳性患者接受 COVID-19 特异性治疗的分析中,发现潜在的 DDI 很常见。虽然低剂量皮质类固醇主要用于 COVID-19 治疗,但与增效型抗逆转录病毒药物合用似乎最有可能发生潜在的 DDI。此外,应注意 NNRTI 合用。