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Arbidol/IFN-α2b therapy for patients with corona virus disease 2019: a retrospective multicenter cohort study
The spread of COVID-19 is accelerating. At present, there is no specific antiviral drugs for COVID-19 outbreak. This is a multicenter retrospective cohort study of patients with laboratory-confirmed COVID-19 infection pneumonia from 3 hospitals in Hubei and Guangdong province, 141 adults (aged ≥18 y...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Published by Elsevier Masson SAS on behalf of Institut Pasteur.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7238991/ https://www.ncbi.nlm.nih.gov/pubmed/32445881 http://dx.doi.org/10.1016/j.micinf.2020.05.012 |
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author | Xu, Ping Huang, Jianping Fan, Zhao Huang, Wendi Qi, Minghua Lin, Xuwen Song, Weidong Yi, Li |
author_facet | Xu, Ping Huang, Jianping Fan, Zhao Huang, Wendi Qi, Minghua Lin, Xuwen Song, Weidong Yi, Li |
author_sort | Xu, Ping |
collection | PubMed |
description | The spread of COVID-19 is accelerating. At present, there is no specific antiviral drugs for COVID-19 outbreak. This is a multicenter retrospective cohort study of patients with laboratory-confirmed COVID-19 infection pneumonia from 3 hospitals in Hubei and Guangdong province, 141 adults (aged ≥18 years) without ventilation were included. Combined group patients were given Arbidol and IFN-α2b, monotherapy group patients inhaled IFN-α2b for 10–14 days. Of 141 COVID-19 patients, baseline clinical and laboratory characteristics were similar between combined group and monotherapy group, that 30% of the patients leucocytes counts were below the normal range and 36.4% of the patients experienced lymphocytopenia. The duration of viral RNA of respiratory tract in the monotherapy group was not longer than that in the combined therapy group. There was no significant differences between two groups. The absorption of pneumonia in the combined group was faster than that in the monotherapy group. We inferred that Arbidol/IFN - 2 b therapy can be used as an effective method to improve the COVID-19 pneumonia of mild patients, although it helpless with accelerating the virus clearance. These results should be verified in a larger prospective randomized environment. |
format | Online Article Text |
id | pubmed-7238991 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Published by Elsevier Masson SAS on behalf of Institut Pasteur. |
record_format | MEDLINE/PubMed |
spelling | pubmed-72389912020-05-20 Arbidol/IFN-α2b therapy for patients with corona virus disease 2019: a retrospective multicenter cohort study Xu, Ping Huang, Jianping Fan, Zhao Huang, Wendi Qi, Minghua Lin, Xuwen Song, Weidong Yi, Li Microbes Infect Article The spread of COVID-19 is accelerating. At present, there is no specific antiviral drugs for COVID-19 outbreak. This is a multicenter retrospective cohort study of patients with laboratory-confirmed COVID-19 infection pneumonia from 3 hospitals in Hubei and Guangdong province, 141 adults (aged ≥18 years) without ventilation were included. Combined group patients were given Arbidol and IFN-α2b, monotherapy group patients inhaled IFN-α2b for 10–14 days. Of 141 COVID-19 patients, baseline clinical and laboratory characteristics were similar between combined group and monotherapy group, that 30% of the patients leucocytes counts were below the normal range and 36.4% of the patients experienced lymphocytopenia. The duration of viral RNA of respiratory tract in the monotherapy group was not longer than that in the combined therapy group. There was no significant differences between two groups. The absorption of pneumonia in the combined group was faster than that in the monotherapy group. We inferred that Arbidol/IFN - 2 b therapy can be used as an effective method to improve the COVID-19 pneumonia of mild patients, although it helpless with accelerating the virus clearance. These results should be verified in a larger prospective randomized environment. Published by Elsevier Masson SAS on behalf of Institut Pasteur. 2020 2020-05-20 /pmc/articles/PMC7238991/ /pubmed/32445881 http://dx.doi.org/10.1016/j.micinf.2020.05.012 Text en © 2020 Published by Elsevier Masson SAS on behalf of Institut Pasteur. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active. |
spellingShingle | Article Xu, Ping Huang, Jianping Fan, Zhao Huang, Wendi Qi, Minghua Lin, Xuwen Song, Weidong Yi, Li Arbidol/IFN-α2b therapy for patients with corona virus disease 2019: a retrospective multicenter cohort study |
title | Arbidol/IFN-α2b therapy for patients with corona virus disease 2019: a retrospective multicenter cohort study |
title_full | Arbidol/IFN-α2b therapy for patients with corona virus disease 2019: a retrospective multicenter cohort study |
title_fullStr | Arbidol/IFN-α2b therapy for patients with corona virus disease 2019: a retrospective multicenter cohort study |
title_full_unstemmed | Arbidol/IFN-α2b therapy for patients with corona virus disease 2019: a retrospective multicenter cohort study |
title_short | Arbidol/IFN-α2b therapy for patients with corona virus disease 2019: a retrospective multicenter cohort study |
title_sort | arbidol/ifn-α2b therapy for patients with corona virus disease 2019: a retrospective multicenter cohort study |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7238991/ https://www.ncbi.nlm.nih.gov/pubmed/32445881 http://dx.doi.org/10.1016/j.micinf.2020.05.012 |
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