The Effect of Recombinant Human Interferon Alpha Nasal Drops to Pre-vent COVID-19 Pneumonia for Medical Staff in an Epidemic Area

被引:31
作者
Meng, Zhongji [1 ,2 ,3 ]
Wang, Tongyu [4 ,5 ]
Chen, Li [1 ]
Chen, Xinhe [1 ]
Li, Longti [1 ]
Qin, Xueqin [1 ]
Li, Hai [4 ,5 ]
Luo, Jie [1 ]
机构
[1] Hubei Univ Med, Taihe Hosp, Novel Coronavinis Pneumonia Prevent & Control Tea, Shiyan 442000, Hubei, Peoples R China
[2] Hubei Univ Med, Taihe Hosp, Inst Biomed Res, Shiyan 442000, Hubei, Peoples R China
[3] Hubei Clin Res Ctr Precise Diag & Treatment Liver, Shiyan 442000, Hubei, Peoples R China
[4] Shanghai Jiao Tong Univ, Sch Med, Dept Gastroenterol, Renji Hosp, Shanghai 200127, Peoples R China
[5] Shanghai Jiao Tong Univ, Chinese Minist Hlth, Shanghai Inst Digest Dis, Key Lab Gastroenterol & Hepatol, Shanghai 200127, Peoples R China
关键词
Coronavirus disease 2019 (COVID-19); respiratory syndrome; prophylaxis; medical staff; thymosin-alpha; 1; IFN-alpha nasal drops;
D O I
10.2174/1568026621666210429083050
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Background: Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), known as Coronavirus disease-2019 (COVID-19), has caused the sixth world's public health emergency. Healthcare staff, as the frontline population fighting the pandemic, are exposed to a high risk of infection. Therefore, developing a protective intervention for medical staff is of significant importance. Objective: The aim of the study was to explore the effectiveness and safety of recombinant human interferon alpha (rhIFN-alpha) nasal drops for the prevention of coronavirus disease 2019 (COVID-19) through administering it to medical staff. Methods: This was a prospective open-label clinical trial with parallel intervention assignment conducted on 2944 medical staff including both doctors and nurses from Taihe Hospital, Shiyan City, Hubei Province, China from January 21, 2020 to July 30, 2020. The participants were bifurcated into two groups of low risk and high risk groups according to the level of direct exposure to COVID-19 patients. The individuals of the low-risk group received rhIFN-alpha nasal drops for one month in addition to first level protection, and the high-risk group received a combination of rhIFN-alpha nasal drops coupled with thymosin-alpha 1 with either second or third-level protection protocol. Moreover, the new-outset of COVID-19 pneumonia diagnosed by chest computed tomography (CT), after thirty days, was the primary outcome. The adverse reactions were recorded in all participants. Results: 2415 of 2944 individuals belonged to the low-risk group, while 529 to the high-risk group. There was no COVID-19 pneumonia in either of the group after thirty days. The pulmonary CT scans were negative for COVID-19 pneumonia in both the groups with no new clinical symptoms. No serious adverse event was observed during the course of the intervention. Conclusion: The rhIFN-alpha nasal drops along with augmented safeguards based on standard physical isolation could effectively protect medical staff against COVID-19 pneumonia.
引用
收藏
页码:920 / 927
页数:8
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