• FluTrackers.com Inc. does not provide medical advice. Information on this web site is collected from various internet resources, and the FluTrackers board of directors makes no warranty to the safety, efficacy, correctness or completeness of the information posted on this site by any author or poster. The information collated here is for instructional and/or discussion purposes only and is NOT intended to diagnose or treat any disease, illness, or other medical condition. Every individual reader or poster should seek advice from their personal physician/healthcare practitioner before considering or using any interventions that are discussed on this website. By continuing to access this website you agree to consult your personal physican before using any interventions posted on this website, and you agree to hold harmless FluTrackers.com Inc., the board of directors, the members, and all authors and posters for any effects from use of any medication, supplement, vitamin or other substance, device, intervention, etc. mentioned in posts on this website, or other internet venues referenced in posts on this website.
  • We are not asking for any donations. Do not donate to any entity who says they are raising funds for us.

J Infect Chemother . Early favipiravir treatment was associated with early defervescence in non-severe COVID-19 patients

tetano

Editor, Senior Moderator
J Infect Chemother


. 2021 Apr 17;S1341-321X(21)00120-3.
doi: 10.1016/j.jiac.2021.04.013. Online ahead of print.
Early favipiravir treatment was associated with early defervescence in non-severe COVID-19 patients


Satoshi Fujii[SUP] 1 [/SUP], Yuta Ibe[SUP] 2 [/SUP], Tomoyuki Ishigo[SUP] 2 [/SUP], Hirotoshi Inamura[SUP] 2 [/SUP], Yusuke Kunimoto[SUP] 2 [/SUP], Yoshihiro Fujiya[SUP] 3 [/SUP], Koji Kuronuma[SUP] 4 [/SUP], Hiromasa Nakata[SUP] 2 [/SUP], Masahide Fukudo[SUP] 2 [/SUP], Satoshi Takahashi[SUP] 3 [/SUP]



Affiliations

Abstract

Introduction: The antiviral drug favipiravir has been shown to have in vitro antiviral activity against severe-acute-respiratory-syndrome-coronavirus-2 (SARS-CoV-2). In this study, we investigated the clinical benefits and initiation of favipiravir treatment in patients with non-severe coronavirus-disease-2019 (COVID-19).
Methods: This study was a single-center retrospective cohort study. Receiver operating characteristic curves were drawn to calculate the area under the curve, and the optimal cut-off values for the time to initiate favipiravir treatment were calculated to predict defervescence within seven days. Univariate and multivariate Cox regression analyses were performed to identify potential influencing factors of defervescence. This was defined as a body temperature of less than 37 ?C for at least 2 days.
Results: Data from 41 patients were used for the efficacy assessment. The days from the onset of fever to defervescence showed a positive correlation with the duration from the onset of fever to initiation of favipiravir treatment (r = 0.548, P < 0.001). The optimal cut-off value was the administration of favipiravir on day 4. Patients were assigned to two groups based on the optimal cut-off value from onset to initiation of favipiravir treatment: early treatment group (within 4-days) and late treatment group (more than 4-days). In the multivariate analysis, when adjusted for age, sex, and days from onset to initiation of favipiravir treatment, the significant factors were male sex and days of initiation of the favipiravir treatment.
Conclusions: We recommend that if favipiravir is to be used for treatment, it should be initiated as early as possible.

Keywords: COVID-19; Defervescence; Early treatment; Favipiravir; SARS-CoV-2.
 
Back
Top Bottom