Zhao Bing, Liu Min, Liu Ping, Peng Yibing, Huang Jun, Li Mengjiao, Wang Yihui, Xu LiLi, Sun Silei, Qi Xing, Ling Yun, Li Jian, Zhang Wenhong, Mao Enqiang, Qu Jieming
Department of Emergency of Ruijin Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.
Department of Gastroenterology, Shanghai Public Health Clinical Center, Shanghai, China.
Front Pharmacol. 2021 Apr 22;12:638556. doi: 10.3389/fphar.2021.638556. eCollection 2021.
Coronavirus disease 2019 (COVID-19) pandemic is continuing to impact multiple countries worldwide and effective treatment options are still being developed. In this study, we investigate the potential of high-dose intravenous vitamin C (HDIVC) in the prevention of moderate COVID-19 disease aggravation. In this retrospective before-after case-matched clinical study, we compare the outcome and clinical courses of patients with moderate COVID-19 patients who were treated with an HDIVC protocol (intravenous injection of vitamin C, 100 mg/kg/day, 1 g/h, for 7 days from admission) during a one-month period (between March 18 and april 18, 2020, HDIVC group) with a control group treated without the HDIVC protocol during the preceding two months (January 18 to March 18, 2020). Patients in the two groups were matched in a 1:1 ratio according to age and gender. The HDIVC and control groups each comprised 55 patients. For the primary outcomes, there was a significant difference in the number of patients that evolved from moderate to severe type between the two groups (HDIVC: 4/55 vs. control: 12/55, relative risk [RR] = 0.28 [0.08, 0.93], = 0.03). Compared to the control group, there was a shorter duration of systemic inflammatory response syndrome (SIRS) ( = 0.0004) during the first week and lower SIRS occurrence (2/21 vs 10/22, = 0.0086) on Day 7 (6-7 days after admission). In addition, HDIVC group had lower C-reactive protein levels ( = 0.005) and higher number of CD4 T cells from Day 0 (on admission) to Day 7 ( = 0.04)." The levels of coagulation indicators, including activated partial thromboplastin time and D-dimer were also improved in the HDIVC compared to the control group on Day 7. HDIVC may be beneficial in limiting disease aggravation in the early stage of COVID-19 pneumonia, which may be related to its improvements on the inflammatory response, immune function and coagulation function. Further randomized controlled trials are required to augment these findings.
2019冠状病毒病(COVID-19)大流行仍在持续影响全球多个国家,有效的治疗方案仍在研发中。在本研究中,我们调查了高剂量静脉注射维生素C(HDIVC)预防中度COVID-19病情加重的潜力。在这项回顾性前后病例匹配临床研究中,我们比较了中度COVID-19患者的结局和临床病程,这些患者在一个月期间(2020年3月18日至4月18日,HDIVC组)接受了HDIVC方案治疗(静脉注射维生素C,100mg/kg/天,1g/小时,从入院起持续7天),并与前两个月(2020年1月18日至3月18日)未接受HDIVC方案治疗的对照组进行比较。两组患者按年龄和性别以1:1的比例匹配。HDIVC组和对照组各有55例患者。对于主要结局,两组之间从中度发展为重度类型的患者数量存在显著差异(HDIVC组:4/55 vs.对照组:12/55,相对风险[RR]=0.28[0.08,0.93],P=0.03)。与对照组相比,第一周全身炎症反应综合征(SIRS)的持续时间更短(P=0.0004),且在第7天(入院后6 - 7天)SIRS的发生率更低(2/21 vs 10/22,P=0.0086)。此外,从第0天(入院时)到第7天,HDIVC组的C反应蛋白水平更低(P=0.005),CD4 T细胞数量更多(P=0.04)。与对照组相比,HDIVC组在第7天的凝血指标水平,包括活化部分凝血活酶时间和D - 二聚体也有所改善。HDIVC可能有助于限制COVID-19肺炎早期的病情加重,这可能与其对炎症反应、免疫功能和凝血功能的改善有关。需要进一步的随机对照试验来加强这些发现。