Liu Jingyuan, Jiang Yuyong, Liu Yao, Pu Lin, Du Chunjing, Li Yuxin, Wang Xiaojing, Ren Jie, Liu Wei, Yang Zhiyun, Chen Zhihai, Song Rui, Xie Wen, Wang Xianbo
Department of Critical Care Medicine, Beijing Ditan Hospital, Capital Medical University, Beijing, China.
Center of Integrative Medicine, Beijing Ditan Hospital, Capital Medical University, Beijing, China.
Front Pharmacol. 2021 Feb 5;11:634266. doi: 10.3389/fphar.2020.634266. eCollection 2020.
Granules (YDJDG) have been newly prescribed as a Chinese herbal formula. This study aimed to compare the efficacy of YDJDG and lopinavir-ritonavir in the treatment of coronavirus disease 2019 (COVID-19). Overall, 131 patients with COVID-19 were included in this study. In addition to standard care, 60 of these patients received YDJDG (YDJDG group) and 71 received lopinavir-ritonavir (lopinavir-ritonavir group). Propensity score matching (PSM) was used to match the characteristics of individuals in the two groups, while the Kaplan-Meier method was used to compare the proportion recovery observed. Cox analysis revealed that YDJDG and CD4 ≥ 660 cells/µL were independent predictive factors of proportion recovery. At baseline, disease types differed between the YDJDG and lopinavir-ritonavir treatment groups. Furthermore, no significant adverse effects or toxicities relevant to YDJDG were observed. The median recovery time was 21 days in the YDJDG group and 27 days in the lopinavir-ritonavir group. After PSM (1:1), 50 patient pairs, YDJDG vs. lopinavir-ritonavir, were analyzed. In the YDJDG group, the proportion of recovered patients was remarkably higher than that observed in the lopinavir-ritonavir group ( = 0.0013), especially for those presenting mild/moderate disease type and CD4 < 660 cells/µL. In the YDJDG group, the mean duration of fever and pulmonary exudative lesions was significantly shorter than that observed in the lopinavir-ritonavir group ( = 0.0180 and = 0.0028, respectively). YDJDG reveals the potential to hasten the recovery period in COVID-19 patients with mild/moderate disease type or CD4 < 660 cells/µL by shortening the mean duration of fever and pulmonary exudative lesions.
颗粒剂(YDJDG)是一种新开具的中药配方。本研究旨在比较YDJDG与洛匹那韦 - 利托那韦治疗2019冠状病毒病(COVID - 19)的疗效。总体而言,本研究纳入了131例COVID - 19患者。除标准治疗外,其中60例患者接受YDJDG(YDJDG组),71例接受洛匹那韦 - 利托那韦(洛匹那韦 - 利托那韦组)。采用倾向评分匹配(PSM)来匹配两组个体的特征,同时使用Kaplan - Meier方法比较观察到的恢复比例。Cox分析显示,YDJDG和CD4≥660个细胞/μL是恢复比例的独立预测因素。在基线时,YDJDG组和洛匹那韦 - 利托那韦治疗组的疾病类型不同。此外,未观察到与YDJDG相关的显著不良反应或毒性。YDJDG组的中位恢复时间为21天,洛匹那韦 - 利托那韦组为27天。经过PSM(1:1)后,分析了50对患者,即YDJDG组与洛匹那韦 - 利托那韦组。在YDJDG组中,恢复患者的比例显著高于洛匹那韦 - 利托那韦组(= 0.0013),尤其是对于那些表现为轻度/中度疾病类型且CD4 < 660个细胞/μL的患者。在YDJDG组中,发热和肺部渗出性病变的平均持续时间明显短于洛匹那韦 - 利托那韦组(分别为= 0.0180和= 0.0028)。YDJDG显示出通过缩短发热和肺部渗出性病变的平均持续时间,加速轻度/中度疾病类型或CD4 < 660个细胞/μL的COVID - 19患者恢复期的潜力。