Real-world experience with molnupiravir during the period of SARS-CoV-2 Omicron variant dominance.

COVID-19 Molnupiravir Omicron Real-world experience SARS-CoV-2 Treatment

Journal

Pharmacological reports : PR
ISSN: 2299-5684
Titre abrégé: Pharmacol Rep
Pays: Switzerland
ID NLM: 101234999

Informations de publication

Date de publication:
Dec 2022
Historique:
received: 28 06 2022
accepted: 17 08 2022
revised: 12 08 2022
pubmed: 25 8 2022
medline: 15 12 2022
entrez: 24 8 2022
Statut: ppublish

Résumé

The real-world effectiveness of molnupiravir (MOL) during the dominance of Omicron SARS-CoV-2 lineage is urgently needed since the available data relate to the period of circulation of other viral variants. Therefore, this study assessed the efficacy of MOL in patients hospitalized for COVID-19 in a real-world clinical practice during the wave of Omicron infections. Among 11,822 patients hospitalized after 1 March 2020 and included in the SARSTer national database, 590 were treated between 1 January and 30 April 2022, a period of dominance of the Omicron SARS-CoV-2 variant. MOL was administered to 203 patients, whereas 387 did not receive any antiviral regimen. Both groups were similar in terms of sex, BMI and age allowing for direct comparisons. Patients who did not receive antiviral therapy significantly more often required the use of Dexamethasone and Baricitinib. Treatment with MOL resulted in a statistically significant reduction in mortality during the 28-day follow-up (9.9 vs. 16.3%), which was particularly evident in the population of patients over 80 years of age treated in the first 5 days of the disease (14.6 vs. 35.2%). MOL therapy did not affect the frequency of the need for mechanical ventilation, but patients treated with MOL required oxygen supplementation less frequently than those without antivirals (31.7 vs. 49.2%). The time of hospitalization did not differ between groups. The use of molnupiravir in patients hospitalized for COVID-19 during the dominance of Omicron variant reduced mortality. This effect is particularly evident in patients over 80 years of age.

Sections du résumé

BACKGROUND BACKGROUND
The real-world effectiveness of molnupiravir (MOL) during the dominance of Omicron SARS-CoV-2 lineage is urgently needed since the available data relate to the period of circulation of other viral variants. Therefore, this study assessed the efficacy of MOL in patients hospitalized for COVID-19 in a real-world clinical practice during the wave of Omicron infections.
METHODS METHODS
Among 11,822 patients hospitalized after 1 March 2020 and included in the SARSTer national database, 590 were treated between 1 January and 30 April 2022, a period of dominance of the Omicron SARS-CoV-2 variant. MOL was administered to 203 patients, whereas 387 did not receive any antiviral regimen. Both groups were similar in terms of sex, BMI and age allowing for direct comparisons.
RESULTS RESULTS
Patients who did not receive antiviral therapy significantly more often required the use of Dexamethasone and Baricitinib. Treatment with MOL resulted in a statistically significant reduction in mortality during the 28-day follow-up (9.9 vs. 16.3%), which was particularly evident in the population of patients over 80 years of age treated in the first 5 days of the disease (14.6 vs. 35.2%). MOL therapy did not affect the frequency of the need for mechanical ventilation, but patients treated with MOL required oxygen supplementation less frequently than those without antivirals (31.7 vs. 49.2%). The time of hospitalization did not differ between groups.
CONCLUSIONS CONCLUSIONS
The use of molnupiravir in patients hospitalized for COVID-19 during the dominance of Omicron variant reduced mortality. This effect is particularly evident in patients over 80 years of age.

Identifiants

pubmed: 36001284
doi: 10.1007/s43440-022-00408-6
pii: 10.1007/s43440-022-00408-6
pmc: PMC9400562
doi:

Substances chimiques

molnupiravir YA84KI1VEW
Hydroxylamines 0
Antiviral Agents 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1279-1285

Commentaires et corrections

Type : ErratumIn

Informations de copyright

© 2022. The Author(s).

Références

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Auteurs

Robert Flisiak (R)

Department of Infectious Diseases and Hepatology, Medical University of Białystok, 15-540, ul. Żurawia 14, Białystok, Poland. robert.flisiak1@gmail.com.

Dorota Zarębska-Michaluk (D)

Department of Infectious Diseases, Jan Kochanowski University, Kielce, Poland.
Provincial Hospital, Kielce, Poland.

Magdalena Rogalska (M)

Department of Infectious Diseases and Hepatology, Medical University of Białystok, 15-540, ul. Żurawia 14, Białystok, Poland.

Justyna Anna Kryńska (JA)

Department of Infectious Diseases and Hepatology, Medical University of Białystok, 15-540, ul. Żurawia 14, Białystok, Poland.

Justyna Kowalska (J)

Department of Adults' Infectious Diseases, Medical University of Warsaw, Warsaw, Poland.

Ewa Dutkiewicz (E)

ZOZ, Busko Zdroj, Poland.
Jan Kochanowski University, Collegium Medicum, Kielce, Poland.

Krystyna Dobrowolska (K)

Department of Infectious Diseases, Jan Kochanowski University, Kielce, Poland.

Jerzy Jaroszewicz (J)

Department of Infectious Diseases and Hepatology, Medical University of Silesia, Katowice, Poland.

Anna Moniuszko-Malinowska (A)

Department of Infectious Diseases and Neuroinfections, Medical University of Białystok, Białystok, Poland.

Marta Rorat (M)

Department of Forensic Medicine, Wrocław Medical University, Wrocław, Poland.

Regina Podlasin (R)

IV-th Department, Hospital for Infectious Diseases, Warsaw, Poland.

Olga Tronina (O)

Department of Transplantation Medicine, Nephrology, and Internal Diseases, Medical University of Warsaw, Warsaw, Poland.

Piotr Rzymski (P)

Department of Environmental Medicine, Poznan University of Medical Sciences, Poznan, Poland.

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