Clinical efficacy of Lopinavir-Ritonavir combined with interferon alpha in COVID-19
Q4 Medicine
Y. Wang, T. Suo, H. Fan, K. Zhao, J. Zou, D. Wu, G. Tang, G. Chen
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引用次数: 2
Abstract
Objective: To evaluate the clinical efficacy of Lopinavir-Ritonavir combined with interferon alpha on coronavirus disease 2019 (COVID-19). Methods: A prospective and real-world observational clinical research was conducted on COVID-19 cases who were admitted to the Renmin Hospital of Wuhan University from January 25, 2020 to February 12, 2020. Of the 109 cases involved, 58 cases were treated with interferon alpha (group A), while 58 cases were treated with Lopinavir-Ritonavir combined with interferon alpha (group B). The recent outcomes were compared between the two groups by Kruskal Wallis test or Chi square test. Results: The baseline data of the two groups were basically the same. On the 7th day after treatment, the lung inflammation in group B was higher than in group A, and the leukocyte count and neutrophil count in the normal range increased as compared with the baseline value in group B. On the 14th day after treatment, the leukocyte count, lymphocyte count, CD4/CD8 cell count increased as compared with the baseline value, while CRP decreased from baseline in the B group, with statistically significant differnce. Conclusion: Lopinavir-Ritonavir combined with interferon alpha can accelerate the improvement of pulmonary inflammation, and increase the levels of immune cells in COVID-19 patients. © 2021, Editorial Board of Medical Journal of Wuhan University. All right reserved.
洛匹那韦-利托那韦联合α干扰素治疗COVID-19的临床疗效观察
目的:评价洛匹那韦-利托那韦联合干扰素治疗冠状病毒病2019 (COVID-19)的临床疗效。方法:对2020年1月25日至2020年2月12日武汉大学人民医院收治的新冠肺炎病例进行前瞻性和现实观察性临床研究。109例患者中,干扰素治疗组58例(A组),洛匹那韦-利托那韦联合干扰素治疗组58例(B组)。采用Kruskal Wallis检验或卡方检验比较两组近期疗效。结果:两组患者基线资料基本相同。治疗后第7天,B组肺部炎症程度高于A组,正常范围内白细胞计数、中性粒细胞计数较B组基线值升高。治疗后第14天,B组白细胞计数、淋巴细胞计数、CD4/CD8细胞计数较基线值升高,CRP较基线值下降,差异均有统计学意义。结论:洛匹那韦-利托那韦联合干扰素可加速COVID-19患者肺部炎症的改善,提高免疫细胞水平。©2021,武汉大学医学杂志编辑委员会。版权所有。
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