使用预后量表评估新型冠状病毒感染中度和重度病程患者使用抗细胞因子药物的效果

S. V. Nagumanov, A. T. Abdrashitova, E. A. Popov
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引用次数: 0

摘要

目的在一项单中心回顾性队列研究中,根据预后量表对新冠状病毒感染中重度病程患者的临床结果进行预测,分析抗细胞因子药物(托珠单抗、奥洛珠单抗和沙利单抗)的使用效果。回顾性队列研究包括三组患者,分别使用托珠单抗(65 例)、奥洛珠单抗(56 例)和沙利单抗(26 例)。所有患者均于2021年1月至8月期间在Аlexandro-Mariinskaya地区临床医院基础上为COVID-19患者改建的传染病医院接受治疗。入院时和用药 2 天后,使用预后量表预测患者的病程严重程度和预后:4C 死亡率评分、COVID-GRAM、SHOCS-COVID。使用 4C 死亡率评分表对抗细胞因子药物的使用效果进行比较分析后发现,接受托珠单抗(p = 0.002)和沙利单抗(p = 0.031)治疗组的临床预后进一步恶化。在使用 COVID-GRAM 预测量表时,托西珠单抗组(p = 0.004)和奥利珠单抗组(p = 0.005)的预后也进一步恶化。SHOCS-COVID量表显示,托西珠单抗组的预后进一步恶化(p = 0,001)。结论:对中重度COVID-19患者使用抗IL-6及其受体的单克隆抗体药物,在用药2天后,临床预后并没有明显的积极变化。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The use of prognostic scales to assess the effectiveness of the use of anti-cytokine drugs in patients with moderate and severe course of a new coronavirus infection
The aim. To analyze the effectiveness of the use of anti-cytokine drugs (tocilizumab, olokizumab and sarilumab) in a single-center retrospective cohort study based on the prediction of clinical outcomes using prognostic scales, with a single administration in patients with moderate to severe course of a new coronavirus infection.Materials and methods. The retrospective cohort study included three groups of patients with single administration of tocilizumab (65 patients), olokizumab (56 patients) and sarilumab (26 patients). All patients were treated in a repurposed infectious diseases hospital for patients with COVID-19 on the basis of Аlexandro-Mariinskaya Regional Clinical Hospital in the period January- August 2021. Upon admission to the hospital and 2 days after administration of the drug, patients were predicted the severity of the course and outcome using prognostic scales: 4C Mortality Score, COVID-GRAM, SHOCS-COVID.Results. A comparative analysis of the effectiveness of the use of anti-cytokine drugs using the 4C Mortality Score scale revealed a further deterioration in the prognosis of clinical outcome in the groups receiving tocilizumab (p = 0,002) and sarilumab (p = 0,031). When using the COVID-GRAM predictive scale, further deterioration of the prognosis was also noted in the tocilizumab (p = 0,004) and olokizumab (p = 0,005) groups. The SHOCS-COVID scale showed a further deterioration in the prognosis in the tocilizumab group (p = 0,001).Conclusion. The use of drugs based on monoclonal antibodies against IL-6 and its receptors in patients with moderate to severe COVID-19 did not reveal significant positive dynamics in changing the prognosis of clinical outcome 2 days after administration of these drugs.
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