Assessing the Burden and Cost of COVID-19 Across Variants in Commercially Insured Immunocompromised Populations in the United States: Updated Results and Trends from the Ongoing EPOCH-US Study.

COVID-19 Cancer Chronic kidney disease Epidemiology Healthcare resource utilization Immune suppression Immunocompromised Primary immunodeficiency Transplant

Journal

Advances in therapy
ISSN: 1865-8652
Titre abrégé: Adv Ther
Pays: United States
ID NLM: 8611864

Informations de publication

Date de publication:
13 Jan 2024
Historique:
received: 21 09 2023
accepted: 28 11 2023
medline: 13 1 2024
pubmed: 13 1 2024
entrez: 12 1 2024
Statut: aheadofprint

Résumé

EPOCH-US is an ongoing, retrospective, observational cohort study among individuals identified in the Healthcare Integrated Research Database (HIRD These updated results showed a 2.9% prevalence of immune compromise in the population. From April 2020 through December 2022, the overall IR of COVID-19 was 115.7 per 1000 patient-years in the composite IC cohort and 77.8 per 1000 patient-years in the HIRD cohort. The composite IC cohort had a 15.4% hospitalization rate with an average cost of $42,719 for first COVID-19 hospitalization. Comparatively, the HIRD cohort had a 3.7% hospitalization rate with an average cost of $28,848 for first COVID-19 hospitalization. Compared to the general population, IC individuals had 4.3 to 23 times greater risk of hospitalization with first diagnosis of COVID-19. Between January and December 2022, hospitalizations associated with first COVID-19 diagnosis cost over $1 billion, with IC individuals (~ 3% of the population) generating $310 million (31%) of these costs. While only 2.9% of the population, IC individuals had a higher risk of COVID-19 hospitalization and incurred higher healthcare costs across variants. They also disproportionately accounted for over 30% of total costs for first COVID-19 hospitalization in 2022, amounting to ~ $310 million. These data highlight the need for additional preventive measures to decrease the risk of developing severe COVID-19 outcomes in vulnerable IC populations.

Identifiants

pubmed: 38216825
doi: 10.1007/s12325-023-02754-0
pii: 10.1007/s12325-023-02754-0
doi:

Types de publication

Journal Article

Langues

eng

Informations de copyright

© 2024. The Author(s).

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Auteurs

Amita Ketkar (A)

Carelon Research, Wilmington, DE, USA. amitagirish.ketkar@carelon.com.

Vincent Willey (V)

Carelon Research, Wilmington, DE, USA.

Lisa Glasser (L)

AstraZeneca, Biopharmaceuticals Medical, Wilmington, DE, USA.

Casey Dobie (C)

Xcenda, a Cencora company, Conshohocken, PA, USA.

Cachet Wenziger (C)

Carelon Research, Wilmington, DE, USA.

Chia-Chen Teng (CC)

Carelon Research, Wilmington, DE, USA.

Christine Dube (C)

AstraZeneca, Biopharmaceuticals Medical, Wilmington, DE, USA.

Sunny Hirpara (S)

AstraZeneca, Biopharmaceuticals Medical, Wilmington, DE, USA.

Dennis Cunningham (D)

Henry Ford Health, Detroit, MI, USA.

Monica Verduzco-Gutierrez (M)

UT Health San Antonio, San Antonio, TX, USA.

Classifications MeSH