Gao Xiaofang, Ma Chunxia, Ma Yujie, Wang Xiaoqi, Wei Jianhua, Feng Tao, Zhao Guixia, Xu Lin, Zhou Wei, Zheng Xiwei, Zhao Qian, Cao Xiangyuan
Department of Intensive Care Unit, People's Hospital of Ningxia Hui Autonomous Region, Yinchuan 750001, Ningxia Hui Autonomous Region, China.
General Hospital of Ningxia Medical University, Yinchuan 750004, Ningxia Hui Autonomous Region, China.
Zhonghua Wei Zhong Bing Ji Jiu Yi Xue. 2020 Dec;32(12):1423-1427. doi: 10.3760/cma.j.cn121430-20201019-00679.
To investigate the clinical efficacy and short-term and long-term adverse reactions for different antiviral regiments for coronavirus disease 2019 (COVID-19) in Ningxia Hui Autonomous Region during hospitalization and follow-up in 3 months.
A single-center retrospective study was conducted to enroll the COVID-19 patients in isolation ward of the only designated hospital to receive COVID-19 patients (the Fourth People's Hospital of Ningxia Hui Autonomous Region) when the authors were assigned by the Ningxia Health Commission as experts from January 20, 2020 to March 15, 2020. According to the antiviral regimen, the patients were divided into conventional antiviral group and unconventional antiviral group. The conventional antiviral group received α-interferon combined with Lopinavir/Ritonavir (LPV/R). The unconventional antiviral group was given α-interferon combined with LPV/R and Abidor or Ribavirin or Chloroquine. The patients were divided into mild (13 cases), ordinary (45 cases), severe (14 cases) and critical (1 case) types. The clinical data, length of hospital stay, the first 2019 novel coronavirus (2019-nCoV) nucleic acid negative recovery time, cost of hospitalization, 2019-nCoV nucleic acid positive reversal after 14 days of discharge, and the combination of hormones and antibiotics were collected. The differences in blood routine, liver function, blood lipid level and adverse reactions of antiviral drugs during hospitalization were compared between the two groups at 1, 3 and 7 days after admission and 1 and 3 months after discharge.
(1) General information: a total of 75 patients with confirmed COVID-19 were admitted, and 73 patients were eventually enrolled, including 47 cases in the conventional antiviral group and 26 cases in the unconventional antiviral group. Patients with different clinical classification were analyzed, the higher the clinical classification and the patients' age, the higher the proportion of primary diseases and the cost of treatment, and the longer the length of hospital stay. Compared with conventional antiviral group, in unconventional antiviral group the percentage of severe and critical patients were higher [34.6% (9/26) vs. 10.6% (5/47), 3.8% (1/26) vs. 0 (0/47)], the length of hospital stay (days: 16.1±5.6 vs. 11.6±3.3), first nucleic acid negative recovery time (days: 12.4±4.5 vs. 10.0±3.5) were longer, and hospitalization cost was higher [Yuan: 11 984.2 (9 000.6, 24 424.7) vs. 8 140.4 (6 715.7,9 707.7)], with statistically significant differences (all P < 0.05). There were no significant differences in gender, age, proportion of patients with primary diseases and nucleic acid positive reversal rate after 14 days of discharge between the unconventional and conventional antiviral groups (all P > 0.05). (2) Laboratory tests: during the hospitalization, white blood cell count (WBC), platelet count (PLT), total bilirubin (TBil) and three acyl glycerin (TG) levels were first increased and then reduced, lymphocyte count (LYM) was first decreased and then increased in two groups. In the unconventional antiviral group, WBC [(6.53±2.78)×10/L], PLT [(250.77±96.12)×10/L], and TG [(1.94±0.96) μmol/L] all reached their peak values at 7 days after admission. TBil peaked at 3 days after admission, which was (23.69±12.14) μmol/L, and LYM reached the peak 1 month after discharge, which was (1.82±0.50)×10/L; however, there was no statistical significance among the above indicators between two groups. There were no statistically significant differences in alanine aminotransferase (ALT), aspartate aminotransferase (AST) and total cholesterol (TC) between the two groups at each time point. (3) The ratio of combined use of hormones in the non-antiviral group was significantly higher than that in the conventional antiviral group [26.9% (7/26) vs. 4.3% (2/47), P < 0.05].
Age and associated primary diseases are related to the severity of COVID-19 patients. Unconventional antiviral treatment regimens are mostly used for severe COVID-19 patients whose ucleic acid did not turn negative for a long time. Individual antiviral therapy can be used based on the patients' response and tolerance to drugs.
探讨宁夏回族自治区2019冠状病毒病(COVID-19)不同抗病毒方案在住院期间及3个月随访中的临床疗效及短期和长期不良反应。
采用单中心回顾性研究,纳入2020年1月20日至2020年3月15日宁夏回族自治区卫生健康委指派作者作为专家时,在唯一指定收治COVID-19患者的医院(宁夏回族自治区第四人民医院)隔离病房的COVID-19患者。根据抗病毒方案,将患者分为常规抗病毒组和非常规抗病毒组。常规抗病毒组接受α-干扰素联合洛匹那韦/利托那韦(LPV/R)治疗。非常规抗病毒组给予α-干扰素联合LPV/R及阿比多尔或利巴韦林或氯喹。将患者分为轻型(13例)、普通型(45例)、重型(14例)和危重型(1例)。收集患者的临床资料、住院时间、首次新型冠状病毒(2019-nCoV)核酸转阴时间、住院费用、出院14天后2019-nCoV核酸复阳情况以及激素和抗生素联合使用情况。比较两组患者入院后1、3、7天及出院后1、3个月时血常规、肝功能、血脂水平及住院期间抗病毒药物不良反应的差异。
(1)一般资料:共收治确诊COVID-19患者75例,最终纳入73例,其中常规抗病毒组47例,非常规抗病毒组26例。对不同临床分型患者进行分析,临床分型越高、患者年龄越大,基础疾病比例及治疗费用越高,住院时间越长。与常规抗病毒组相比,非常规抗病毒组重型和危重型患者比例更高[34.6%(9/26)比10.6%(5/47),3.8%(1/26)比0(0/47)],住院时间(天:16.1±5.6比11.6±3.3)、首次核酸转阴时间(天:12.4±4.5比10.0±3.5)更长,住院费用更高[元:11 984.2(9 000.6,24 424.7)比8 140.4(6 715.7,9 707.7)],差异均有统计学意义(均P<0.05)。非常规抗病毒组与常规抗病毒组在性别、年龄、基础疾病患者比例及出院14天后核酸复阳率方面差异均无统计学意义(均P>0.05)。(2)实验室检查:住院期间,两组白细胞计数(WBC)、血小板计数(PLT)、总胆红素(TBil)和三酰甘油(TG)水平均先升高后降低,淋巴细胞计数(LYM)先降低后升高。非常规抗病毒组WBC[(6.53±2.78)×10⁹/L]、PLT[(250.77±96.12)×10⁹/L]和TG[(1.94±0.96)μmol/L]均在入院后7天达到峰值。TBil在入院后3天达到峰值,为(23.69±12.14)μmol/L,LYM在出院后1个月达到峰值,为(1.82±0.50)×10⁹/L;但上述指标两组间差异均无统计学意义。两组各时间点丙氨酸氨基转移酶(ALT)、天冬氨酸氨基转移酶(AST)和总胆固醇(TC)差异均无统计学意义。(3)非常规抗病毒组激素联合使用比例显著高于常规抗病毒组[26.9%(7/26)比4.3%(2/47),P<0.05]。
年龄及基础疾病与COVID-19患者病情严重程度相关。非常规抗病毒治疗方案多用于核酸长时间未转阴的重型COVID-19患者。可根据患者对药物的反应及耐受性采用个体化抗病毒治疗。