Early Use of Remdesivir and Risk of Disease Progression in Hospitalized Patients With Mild to Moderate COVID-19.


Journal

Clinical therapeutics
ISSN: 1879-114X
Titre abrégé: Clin Ther
Pays: United States
ID NLM: 7706726

Informations de publication

Date de publication:
03 2022
Historique:
received: 20 10 2021
revised: 08 01 2022
accepted: 10 01 2022
pubmed: 6 2 2022
medline: 28 4 2022
entrez: 5 2 2022
Statut: ppublish

Résumé

Preliminary data suggest that remdesivir may influence the course of COVID-19 according to the duration of pre-admission symptoms. We aim to evaluate whether early use of remdesivir is associated with a reduced COVID-19 progression in a homogeneous cohort of patients with mild to moderate COVID-19. This prospective, observational study included patients with COVID-19 pneumonia treated with remdesivir at the University Hospital of Pisa (Italy) from September 2020 to January 2021. According to national recommendations, remdesivir was prescribed in patients with pneumonia who required oxygen supplementation by nasal cannula or mask but without the need for high-flow nasal cannula, non-invasive or invasive mechanical ventilation and had symptoms from no more than 10 days. Patients who received early (≤5 days from onset of symptoms) versus late (>5 days from onset of symptoms) remdesivir were compared. The primary outcome was a composite of high-flow nasal cannula, non-invasive or invasive mechanical ventilation, or death. A multivariate logistic regression analysis was performed to identify factors independently associated with the composite endpoint. Among 312 consecutive patients with COVID-19 pneumonia who received remdesivir, 90 (28.8%) received early remdesivir, whereas 222 (71.2%) received late remdesivir. Twenty-nine patients (32.2%) in the early-remdesivir group versus 104 patients (46.8%) in the late-remdesivir group met the primary end point (P = 0.018). On multivariate analysis, a history of dyspnea at home (odds ratio = 2.53; 95% CI, 1.55-4.12; P < 0.001) was the strongest factor independently associated with the progression to severe COVID-19, whereas early-remdesivir use was a protective factor (odds ratio = 0.49; 95% CI, 0.27-0.87; P = 0.015). The delayed admission to the hospital was associated with a delayed administration of remdesivir. The early use of remdesivir (<5 days from symptoms onset) may reduce COVID-19 progression. The identification of patients who need early hospitalization and early remdesivir may provide clinical benefit in patients with COVID-19.

Identifiants

pubmed: 35120742
pii: S0149-2918(22)00012-1
doi: 10.1016/j.clinthera.2022.01.007
pmc: PMC8761549
pii:
doi:

Substances chimiques

remdesivir 3QKI37EEHE
Adenosine Monophosphate 415SHH325A
Alanine OF5P57N2ZX

Types de publication

Journal Article Observational Study Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

364-373

Informations de copyright

Copyright © 2022 Elsevier Ltd. All rights reserved.

Références

Clin Infect Dis. 2022 Apr 28;74(8):1450-1458
pubmed: 34265054
Lancet. 2020 May 16;395(10236):1569-1578
pubmed: 32423584
J Antimicrob Chemother. 2021 Nov 12;76(12):3296-3302
pubmed: 34473275
N Engl J Med. 2022 Jan 27;386(4):305-315
pubmed: 34937145
N Engl J Med. 2021 Mar 4;384(9):795-807
pubmed: 33306283
Clin Microbiol Infect. 2021 Mar;27(3):389-395
pubmed: 33359375
Sci Adv. 2021 Jan 1;7(1):
pubmed: 33187978
N Engl J Med. 2020 Nov 5;383(19):1813-1826
pubmed: 32445440
N Engl J Med. 2021 Feb 25;384(8):693-704
pubmed: 32678530
N Engl J Med. 2021 Feb 11;384(6):497-511
pubmed: 33264556
JAMA. 2020 Sep 15;324(11):1048-1057
pubmed: 32821939
Lancet. 2021 May 01;397(10285):1637-1645
pubmed: 33933206
Open Forum Infect Dis. 2020 Nov 19;7(12):ofaa563
pubmed: 33365358
Clin Infect Dis. 2022 Aug 24;75(1):e450-e458
pubmed: 34596223
Infect Dis Ther. 2021 Dec;10(4):2479-2488
pubmed: 34435337

Auteurs

Marco Falcone (M)

Infectious Diseases Unit, Department of Clinical and Experimental Medicine, Azienda Ospedaliera Universitaria Pisana, Pisa, Italy. Electronic address: marco.falcone@unipi.it.

Lorenzo Roberto Suardi (LR)

Infectious Diseases Unit, Department of Clinical and Experimental Medicine, Azienda Ospedaliera Universitaria Pisana, Pisa, Italy.

Giusy Tiseo (G)

Infectious Diseases Unit, Department of Clinical and Experimental Medicine, Azienda Ospedaliera Universitaria Pisana, Pisa, Italy.

Chiara Barbieri (C)

Infectious Diseases Unit, Department of Clinical and Experimental Medicine, Azienda Ospedaliera Universitaria Pisana, Pisa, Italy.

Lisa Giusti (L)

Infectious Diseases Unit, Department of Clinical and Experimental Medicine, Azienda Ospedaliera Universitaria Pisana, Pisa, Italy.

Valentina Galfo (V)

Infectious Diseases Unit, Department of Clinical and Experimental Medicine, Azienda Ospedaliera Universitaria Pisana, Pisa, Italy.

Arianna Forniti (A)

Infectious Diseases Unit, Department of Clinical and Experimental Medicine, Azienda Ospedaliera Universitaria Pisana, Pisa, Italy.

Claudio Caroselli (C)

Infectious Diseases Unit, Department of Clinical and Experimental Medicine, Azienda Ospedaliera Universitaria Pisana, Pisa, Italy.

Leonardo Della Sala (L)

Infectious Diseases Unit, Department of Clinical and Experimental Medicine, Azienda Ospedaliera Universitaria Pisana, Pisa, Italy.

Sara Tempini (S)

Infectious Diseases Unit, Department of Clinical and Experimental Medicine, Azienda Ospedaliera Universitaria Pisana, Pisa, Italy.

Chukwuma Okoye (C)

Geriatrics Unit, Department of Clinical and Experimental Medicine, University of Pisa, Pisa, Italy.

Fabio Monzani (F)

Geriatrics Unit, Department of Clinical and Experimental Medicine, University of Pisa, Pisa, Italy.

Francesco Menichetti (F)

Infectious Diseases Unit, Department of Clinical and Experimental Medicine, Azienda Ospedaliera Universitaria Pisana, Pisa, Italy.

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH