Favipiravir therapy for patients with covid-19 pneumonia: An observational study

Pneumonia in patients with COVID-19 is sometimes severe and life-threatening, and currently there is no specific effective drug approved for COVID-19 treatment. Favipiravir is a pyrazine analog inhibiting RNA virus RNA dependent RNA polymerase with antiviral activity against SARS-CoV-2. An observati...

Full description

Saved in:
Bibliographic Details
Main Authors: Supawadee Suppadungsuk, Thananya Wongsinin, Sirawat Srichatrapimuk, Suppachok Kirdlarp, Kulapong Jayanama, Kanin Thammavaranucupt, Dhanesh Pitidhammabhorn, Sithakom Phusanti, Nithita Nanthatanti, Somnuek Sungkanuparph
Other Authors: Faculty of Medicine Ramathibodi Hospital, Mahidol University
Format: Article
Published: 2022
Subjects:
Online Access:https://repository.li.mahidol.ac.th/handle/123456789/78454
Tags: Add Tag
No Tags, Be the first to tag this record!
Institution: Mahidol University
id th-mahidol.78454
record_format dspace
spelling th-mahidol.784542022-08-04T18:01:02Z Favipiravir therapy for patients with covid-19 pneumonia: An observational study Supawadee Suppadungsuk Thananya Wongsinin Sirawat Srichatrapimuk Suppachok Kirdlarp Kulapong Jayanama Kanin Thammavaranucupt Dhanesh Pitidhammabhorn Sithakom Phusanti Nithita Nanthatanti Somnuek Sungkanuparph Faculty of Medicine Ramathibodi Hospital, Mahidol University Medicine Pneumonia in patients with COVID-19 is sometimes severe and life-threatening, and currently there is no specific effective drug approved for COVID-19 treatment. Favipiravir is a pyrazine analog inhibiting RNA virus RNA dependent RNA polymerase with antiviral activity against SARS-CoV-2. An observational study was conducted in confirmed COVID-19 pneumonia patients admitted to a university hospital in Thailand on effectiveness and safety of favipiravir prescribed on a compassionate-use basis. Among COVID-19 patients with pneumonia (n = 37), 54 and 46% had severe and non-severe pneumonia, respectively. Mean ± SD age was 48 ± 3 years, 62% were male and diabetes mellitus and hypertension were the most common comorbidities. Median period from initiation of favipiravir treatment to clinical improvement of patients with severe and non-severe pneumonia was 17 days (95% confidence interval (CI): 9-25) and 9 days (95% CI: 7-11) respectively. Ninety-five percent of patients completely recovered and were discharged within 39 days following admittance; unfortunately, the remaining patients succumbed to severe acute respiratory distress syndrome and multi-organ failure. In conclusion, favipiravir holds promise as a potential drug for treatment of COVID-19 pneumonia, but a larger randomized trial is warranted to confirm its efficacy. 2022-08-04T11:01:02Z 2022-08-04T11:01:02Z 2021-02-04 Article Southeast Asian Journal of Tropical Medicine and Public Health. Vol.52, No.1 (2021), 161-174 26975718 01251562 2-s2.0-85119835401 https://repository.li.mahidol.ac.th/handle/123456789/78454 Mahidol University SCOPUS https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85119835401&origin=inward
institution Mahidol University
building Mahidol University Library
continent Asia
country Thailand
Thailand
content_provider Mahidol University Library
collection Mahidol University Institutional Repository
topic Medicine
spellingShingle Medicine
Supawadee Suppadungsuk
Thananya Wongsinin
Sirawat Srichatrapimuk
Suppachok Kirdlarp
Kulapong Jayanama
Kanin Thammavaranucupt
Dhanesh Pitidhammabhorn
Sithakom Phusanti
Nithita Nanthatanti
Somnuek Sungkanuparph
Favipiravir therapy for patients with covid-19 pneumonia: An observational study
description Pneumonia in patients with COVID-19 is sometimes severe and life-threatening, and currently there is no specific effective drug approved for COVID-19 treatment. Favipiravir is a pyrazine analog inhibiting RNA virus RNA dependent RNA polymerase with antiviral activity against SARS-CoV-2. An observational study was conducted in confirmed COVID-19 pneumonia patients admitted to a university hospital in Thailand on effectiveness and safety of favipiravir prescribed on a compassionate-use basis. Among COVID-19 patients with pneumonia (n = 37), 54 and 46% had severe and non-severe pneumonia, respectively. Mean ± SD age was 48 ± 3 years, 62% were male and diabetes mellitus and hypertension were the most common comorbidities. Median period from initiation of favipiravir treatment to clinical improvement of patients with severe and non-severe pneumonia was 17 days (95% confidence interval (CI): 9-25) and 9 days (95% CI: 7-11) respectively. Ninety-five percent of patients completely recovered and were discharged within 39 days following admittance; unfortunately, the remaining patients succumbed to severe acute respiratory distress syndrome and multi-organ failure. In conclusion, favipiravir holds promise as a potential drug for treatment of COVID-19 pneumonia, but a larger randomized trial is warranted to confirm its efficacy.
author2 Faculty of Medicine Ramathibodi Hospital, Mahidol University
author_facet Faculty of Medicine Ramathibodi Hospital, Mahidol University
Supawadee Suppadungsuk
Thananya Wongsinin
Sirawat Srichatrapimuk
Suppachok Kirdlarp
Kulapong Jayanama
Kanin Thammavaranucupt
Dhanesh Pitidhammabhorn
Sithakom Phusanti
Nithita Nanthatanti
Somnuek Sungkanuparph
format Article
author Supawadee Suppadungsuk
Thananya Wongsinin
Sirawat Srichatrapimuk
Suppachok Kirdlarp
Kulapong Jayanama
Kanin Thammavaranucupt
Dhanesh Pitidhammabhorn
Sithakom Phusanti
Nithita Nanthatanti
Somnuek Sungkanuparph
author_sort Supawadee Suppadungsuk
title Favipiravir therapy for patients with covid-19 pneumonia: An observational study
title_short Favipiravir therapy for patients with covid-19 pneumonia: An observational study
title_full Favipiravir therapy for patients with covid-19 pneumonia: An observational study
title_fullStr Favipiravir therapy for patients with covid-19 pneumonia: An observational study
title_full_unstemmed Favipiravir therapy for patients with covid-19 pneumonia: An observational study
title_sort favipiravir therapy for patients with covid-19 pneumonia: an observational study
publishDate 2022
url https://repository.li.mahidol.ac.th/handle/123456789/78454
_version_ 1763488457100886016