COVID-19, SARS-CoV-2
Conditions
Brief summary
This is an observational cohort study to evaluate real-world vaccine effectiveness and durability of Moderna COVID-19 vaccine among a diverse population at Kaiser Permanente Southern California (KPSC). The primary objective of this study is to evaluate the vaccine effectiveness (VE) of receipt of Moderna COVID-19 vaccine in preventing SARS-CoV-2 infection and severe COVID-19 disease. SARS-CoV-2 infection will be defined as a positive antigen test result as well as a positive molecular diagnostic test among symptomatic or asymptomatic participants or a COVID-19 diagnosis code. Severe COVID-19 disease will be defined as COVID-19 hospitalization or mortality.
Detailed description
This study utilized electronic healthcare data collected within the Kaiser Permanente Southern California (KPSC) integrated healthcare system which provides care to over 4.6 million individuals. Participants in this study received vaccination and were assessed for study outcomes as part of routine care. Vaccination information and study outcome status was assessed using procedure, diagnostic, and laboratory code information. Medical chart review was conducted to assess the association of severe outcomes (hospitalization and death) with COVID-19 illness. Analyses assessing absolute vaccine effectiveness will identify participants who receive Moderna COVID vaccine from the KPSC electronic healthcare database and match them to unvaccinated participants based on age, sex, race/ethnicity, and data of vaccination (index date). Vaccinated and unvaccinated participants will then be followed-up in the database for the occurrence of study outcomes. Cox proportional hazards regression will be used to compare the relative risk of study outcomes by vaccination status. Analyses of relative vaccine effectiveness will identify participants who receive specific dose number and formulation of Moderna COVID vaccine (Group N) from the KPSC electronic healthcare database and match them to a group of vaccinated participants with a different dose/formulation type (i.e. Group n-1). Similar matching criteria will be applied. Both groups will be followed for study outcomes and cox proportional hazards regression will be used to compare the relative risk of study outcomes by vaccination status.
Interventions
None listed
Sponsors
ModernaTX, Inc.
Study design
Observational model
COHORT
Time perspective
RETROSPECTIVE
Eligibility
Sex/Gender
ALL
Age
6 Months to No maximum
Healthy volunteers
Yes
Inclusion criteria
* Aged ≥18 years at index date (participants aged 6 months through 17 years will also be included after Food and Drug Administration \[FDA\] authorization to vaccinate younger age groups) * KPSC member for ≥12 months prior to index date through 14 days after the index date (allowing a 31-day gap)
Exclusion criteria
* Receipt of a COVID-19 vaccine other than Moderna COVID-19 vaccine prior to or on the index date * Receipt of 2 doses of Moderna COVID-19 vaccine \<24 days apart for 2-dose exposed cohort * Receipt of any COVID-19 vaccine \<14 days after the index date * No health care utilization and no vaccination from the 2 years prior to the index date through the index date * Occurrence of a COVID-19 outcome \<14 days after the index date
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Number of Participants With SARS-CoV-2 Infection | Up to 3 years | SARS-CoV-2 infection is defined as a positive antigen test result as well as a positive molecular test or a COVID-19 diagnosis code. |
| Number of Participants With Severe COVID-19 Disease | Up to 3 years | Severe COVID-19 disease includes COVID-19 hospitalization (hospitalization with a SARS-CoV-2 positive test or a COVID-19 diagnosis, or a hospitalization occurring ≤7 days after a SARS-CoV-2 positive test, with chart review to confirm severe COVID-19 symptoms) and COVID-19 mortality (death during COVID-19 hospitalization). |
Countries
United States
Outcome results
None listed