A Descriptive Cohort Study of Drug Utilization Patterns Among Patients Hospitalized With Coronavirus Disease 2019 in the United States, January 2021-February 2022.

COVID-19 Janus kinase inhibitors drug utilization interleukin-6 inhibitors

Journal

Open forum infectious diseases
ISSN: 2328-8957
Titre abrégé: Open Forum Infect Dis
Pays: United States
ID NLM: 101637045

Informations de publication

Date de publication:
Jul 2023
Historique:
received: 17 01 2023
accepted: 06 07 2023
pmc-release: 10 07 2024
medline: 27 7 2023
pubmed: 27 7 2023
entrez: 27 7 2023
Statut: epublish

Résumé

There is a dearth of drug utilization studies for coronavirus disease 2019 (COVID-19) treatments in 2021 and beyond after the introduction of vaccines and updated guidelines; such studies are needed to contextualize ongoing COVID-19 treatment effectiveness studies during these time periods. This study describes utilization patterns for corticosteroids, interleukin-6 (IL-6) inhibitors, Janus kinase inhibitors, and remdesivir among hospitalized adults with COVID-19, over the entire hospitalization, and within hospitalization periods categorized by respiratory support requirements. This descriptive cohort study included United States adults hospitalized with COVID-19 admitted from 1 January 2021 through 1 February 2022; data included HealthVerity claims and hospital chargemaster. The number and distribution of patients were reported for the first 3 drug regimen lines initiated. The cohort included 51 066 patients; the most common initial drug regimens were corticosteroids (23.4%), corticosteroids plus remdesivir (25.1%), and remdesivir (4.4%). IL-6 inhibitors and Janus kinase inhibitors were included in later drug regimens and were more commonly administered with both corticosteroids and remdesivir than with corticosteroids alone. IL-6 inhibitors were more commonly administered than Janus kinase inhibitors when patients received high-flow oxygen or ventilation. These findings provide important context for comparative studies of COVID-19 treatments with study periods extending into 2021 and later. While prescribing generally aligned with National Institutes of Health COVID-19 treatment guidelines during this period, these findings suggest that prescribing preference, potential confounding by indication, and confounding by prior/concomitant use of other therapeutics should be considered in the design and interpretation of comparative studies.

Sections du résumé

Background UNASSIGNED
There is a dearth of drug utilization studies for coronavirus disease 2019 (COVID-19) treatments in 2021 and beyond after the introduction of vaccines and updated guidelines; such studies are needed to contextualize ongoing COVID-19 treatment effectiveness studies during these time periods. This study describes utilization patterns for corticosteroids, interleukin-6 (IL-6) inhibitors, Janus kinase inhibitors, and remdesivir among hospitalized adults with COVID-19, over the entire hospitalization, and within hospitalization periods categorized by respiratory support requirements.
Methods UNASSIGNED
This descriptive cohort study included United States adults hospitalized with COVID-19 admitted from 1 January 2021 through 1 February 2022; data included HealthVerity claims and hospital chargemaster. The number and distribution of patients were reported for the first 3 drug regimen lines initiated.
Results UNASSIGNED
The cohort included 51 066 patients; the most common initial drug regimens were corticosteroids (23.4%), corticosteroids plus remdesivir (25.1%), and remdesivir (4.4%). IL-6 inhibitors and Janus kinase inhibitors were included in later drug regimens and were more commonly administered with both corticosteroids and remdesivir than with corticosteroids alone. IL-6 inhibitors were more commonly administered than Janus kinase inhibitors when patients received high-flow oxygen or ventilation.
Conclusions UNASSIGNED
These findings provide important context for comparative studies of COVID-19 treatments with study periods extending into 2021 and later. While prescribing generally aligned with National Institutes of Health COVID-19 treatment guidelines during this period, these findings suggest that prescribing preference, potential confounding by indication, and confounding by prior/concomitant use of other therapeutics should be considered in the design and interpretation of comparative studies.

Identifiants

pubmed: 37496608
doi: 10.1093/ofid/ofad339
pii: ofad339
pmc: PMC10368445
doi:

Types de publication

Journal Article

Langues

eng

Pagination

ofad339

Informations de copyright

Published by Oxford University Press on behalf of Infectious Diseases Society of America 2023.

Déclaration de conflit d'intérêts

Potential conflicts of interest. S. E. V., P. G., A. B., E. B., E. M. G., N. M. G., and V. F. are employees of Aetion, Inc, with stock options. All other authors report no potential conflicts.

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Auteurs

Sarah E Vititoe (SE)

Aetion, Inc, Scientific Research and Strategy, New York, New York, USA.

Priya Govil (P)

Aetion, Inc, Scientific Research and Strategy, New York, New York, USA.

Aidan Baglivo (A)

Aetion, Inc, Scientific Research and Strategy, New York, New York, USA.

Elisha Beebe (E)

Aetion, Inc, Scientific Research and Strategy, New York, New York, USA.

Elizabeth M Garry (EM)

Aetion, Inc, Scientific Research and Strategy, New York, New York, USA.

Nicolle M Gatto (NM)

Aetion, Inc, Scientific Research and Strategy, New York, New York, USA.

Tamar Lasky (T)

Office of the Commissioner, US Food and Drug Administration, Silver Spring, Maryland, USA.

Aloka Chakravarty (A)

Office of the Commissioner, US Food and Drug Administration, Silver Spring, Maryland, USA.

Marie C Bradley (MC)

Division of Epidemiology, Office of Surveillance and Epidemiology, Center for Drug Evaluation and Research, US Food and Drug Administration, Silver Spring, Maryland, USA.

Silvia Perez-Vilar (S)

Division of Epidemiology, Office of Surveillance and Epidemiology, Center for Drug Evaluation and Research, US Food and Drug Administration, Silver Spring, Maryland, USA.

Donna R Rivera (DR)

Oncology Center of Excellence, US Food and Drug Administration, Silver Spring, Maryland, USA.

Kenneth Quinto (K)

Office of Medical Policy, Center for Drug Evaluation and Research, US Food and Drug Administration, Silver Spring, Maryland, USA.

Andrew Clerman (A)

Division of Pulmonology, Allergy, and Critical Care, Office of Immunology and Inflammation, Office of New Drugs, Center for Drug Evaluation and Research, US Food and Drug Administration, Silver Spring, Maryland, USA.

Anil Rajpal (A)

Division of Rheumatology and Transplant Medicine, Office of Immunology and Inflammation, Office of New Drugs, Center for Drug Evaluation and Research, US Food and Drug Administration, Silver Spring, Maryland, USA.

Vera Frajzyngier (V)

Aetion, Inc, Scientific Research and Strategy, New York, New York, USA.

Classifications MeSH