Early antiviral therapy of abidol combined with lopinavir/ritonavir and recombinant interferon α-2b for patients with COVID-19 in Zhejiang: A multicenter prospective study
10.3760/cma.j.issn.1674-2397.2020.01.003
- VernacularTitle:浙江省新型冠状病毒肺炎患者早期阿比多尔+洛匹那韦/利托那韦+重组干扰素α-2b联合抗病毒治疗的多中心、前瞻性研究
- Author:
Runan WEI
1
;
Nanhong ZHENG
;
Xiangao JIANG
;
Chunlian MA
;
Xiaowei XU
;
Shourong LIU
;
Yongping CHEN
;
Kaijin XU
;
Hainv GAO
;
Jiansheng ZHU
;
Qiang SHU
;
Jifang SHENG
;
Xiaoqiang ZHANG
;
Minghui LI
;
Yan ZHANG
;
Mengjie MA
;
Xuan ZHANG
;
Shibo LI
;
Qiujing WANG
;
Lingjun YING
;
Yongjun ZHANG
;
Yunzhen SHI
;
Lingyan FAN
;
Wanjun YU
;
Huaying WANG
;
Dandan SUN
;
Xiaodong WANG
;
Jichan SHI
;
Yinghu CHEN
;
Xinsheng XIE
;
Yunqing CHEN
;
Weihong WANG
;
Zhaowei TONG
;
Lingling TANG
;
Mengfei ZHU
;
Lingjian ZHANG
;
Lanjuan LI
Author Information
1. 浙江大学医学院附属第一医院 传染病诊治国家重点实验室;杭州 310003
- From:
Chinese Journal of Clinical Infectious Diseases
2020;13(1):9-15
- CountryChina
- Language:Chinese
-
Abstract:
Objective:To compare the efficacy of the combination of abidol, lopinavir/ritonavir plus recombinant interferon α-2b (rIFNα-2b) and the combination of lopinavir/ritonavir plus rIFNα-2b for patients with COVID-19 in Zhejiang province.Methods:A multicenter prospective study was carried out to compare the efficacy of triple combination antiviral therapy and dual combination antiviral therapy in 15 medical institutions of Zhejiang province during January 22 to February 16, 2020. All patients were treated with rIFNα-2b (5 million U, 2 times/d) aerosol inhalation, in addition 196 patients were treated with abidol (200 mg, 3 times/d) + lopinavir/ritonavir (2 tablets, 1 time/12 h) (triple combination group) and 41 patients were treated with lopinavir/ritonavir (2 tablets, 1 time/12 h) (dual combination group). The patients who received triple combination antiviral therapy were further divided into three subgroups: <48 h, 3-5 d and >5 d according the time from the symptom onset to medication starting. The therapeutic efficacy was compared between triple combination group and dual combination group, and compared among 3 subgroups of patients receiving triple combination antiviral therapy. SPSS 17.0 software was used to analyze the data.Results:The virus nucleic acid-negative conversion time in respiratory tract specimens was (12.2±4.7) d in the triple combination group, which was shorter than that in the dual combination group [(15.0±5.0) d] ( t=6.159, P<0.01). The length of hospital stay in the triple combination group [12.0 (9.0, 17.0) d] was also shorter than that in the dual combination group [15.0 (10.0, 18.0) d] ( H=2.073, P<0.05). Compared with the antiviral treatment which was started within after the symptom onset of in the triple combination group, the time from the symptom onset to the viral negative conversion was 13.0 (10.0, 17.0), 17.0 (13.0, 22.0) and 21.0 (18.0, 24.0) d in subgroups of 48 h, 3-5 d and >5 d, respectively ( Z=32.983, P<0.01), while the time from antiviral therapy to viral negative conversion was (11.8±3.9), (13.5±5.1) and (11.2±4.3) d, respectively( Z=6.722, P<0.05). Conclusions:The triple combination antiviral therapy of abidol, lopinavir/litonavir and rIFNα-2b shows shorter viral shedding time and shorter hospitalization time, compared with the dual combination antiviral therapy; and the earlier starting triple combination antiviral therapy will result in better antiviral efficacy.