Author: Yousefi, Bahman; Valizadeh, Saeid; Ghaffari, Hadi; Vahedi, Azadeh; Karbalaei, Mohsen; Eslami, Majid
Title: A global treatments for coronaviruses including COVIDâ€19 Cord-id: qxdakdk0 Document date: 2020_5_11
ID: qxdakdk0
Snippet: In late December 2019 in Wuhan, China, several patients with viral pneumonia were identified as 2019 novel coronavirus (2019â€nCoV). So far, there are no specific treatments for patients with coronavirus diseaseâ€19 (COVIDâ€19), and the treatments available today are based on previous experience with similar viruses such as severe acute respiratory syndromeâ€related coronavirus (SARSâ€CoV), Middle East respiratory syndrome coronavirus (MERSâ€CoV), and Influenza virus. In this article, we h
Document: In late December 2019 in Wuhan, China, several patients with viral pneumonia were identified as 2019 novel coronavirus (2019â€nCoV). So far, there are no specific treatments for patients with coronavirus diseaseâ€19 (COVIDâ€19), and the treatments available today are based on previous experience with similar viruses such as severe acute respiratory syndromeâ€related coronavirus (SARSâ€CoV), Middle East respiratory syndrome coronavirus (MERSâ€CoV), and Influenza virus. In this article, we have tried to reach a therapeutic window of drugs available to patients with COVIDâ€19. Cathepsin L is required for entry of the 2019â€nCoV virus into the cell as target teicoplanin inhibits virus replication. Angiotensinâ€convertingâ€enzyme 2 (ACE2) in soluble form as a recombinant protein can prevent the spread of coronavirus by restricting binding and entry. In patients with COVIDâ€19, hydroxychloroquine decreases the inflammatory response and cytokine storm, but overdose causes toxicity and mortality. Neuraminidase inhibitors such as oseltamivir, peramivir, and zanamivir are invalid for 2019â€nCoV and are not recommended for treatment but protease inhibitors such as lopinavir/ritonavir (LPV/r) inhibit the progression of MERSâ€CoV disease and can be useful for patients of COVIDâ€19 and, in combination with Arbidol, has a direct antiviral effect on early replication of SARSâ€CoV. Ribavirin reduces hemoglobin concentrations in respiratory patients, and remdesivir improves respiratory symptoms. Use of ribavirin in combination with LPV/r in patients with SARSâ€CoV reduces acute respiratory distress syndrome and mortality, which has a significant protective effect with the addition of corticosteroids. Favipiravir increases clinical recovery and reduces respiratory problems and has a stronger antiviral effect than LPV/r. currently, appropriate treatment for patients with COVIDâ€19 is an ACE2 inhibitor and a clinical problem reducing agent such as favipiravir in addition to hydroxychloroquine and corticosteroids.
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