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| Funder | NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES |
|---|---|
| Recipient Organization | William Beaumont Hospital Research Inst |
| Country | United States |
| Start Date | Jan 11, 2021 |
| End Date | Dec 31, 2025 |
| Duration | 1,815 days |
| Number of Grantees | 1 |
| Roles | Principal Investigator |
| Data Source | NIH (US) |
| Grant ID | 10750955 |
Incorporation of multilevel ontologies of adverse events and vaccines for vaccine safety surveillance PROJECT SUMMARY Vaccines face tougher safety standards than most pharmaceutical products because they are given to healthy people, often children. Effective and rigorous analyses of post-vaccination adverse events
(AEs) is critical to ensure the safety of vaccines. The Vaccine Adverse Event Reporting System (VAERS) is a national vaccine safety surveillance program which contains spontaneous reports from 1990 to present. Statistical approaches have been used on VAERS to extract important signals hidden in this large, complex database and offer a hypothesis-free view of the safety characteristics in
the underlying data. However, existing methods may miss detecting serious AEs due to modeling under the false assumption of independence between different types of AEs. In response to the FOA, PA-18-873, this proposal addresses the specific objective: “creation/evaluation of statistical methodologies for analyzing data on vaccine safety, including data
available from existing data sources such as passive reporting systems or healthcare databases.” We propose to develop a series of methods for vaccine safety surveillance while incorporating adverse event ontology as well as vaccine ontology. Specifically, we will use the Medical Dictionary for Regulatory Activities (MedDRA) and the vaccine ontology (VO) to form the basis of our models for
systematically mining and monitoring safety signals. To the best of our knowledge, this is the first attempt to directly incorporate AE and vaccine ontologies in the signal detection method. Multiple AEs may individually be rare enough to go undetected, but if they are related, they can borrow strength
from each other to increase the chance of being flagged. Furthermore, borrowing strength induces shrinkage of related AEs, thereby also reducing headline-grabbing false positives. Additionally, multiple AEs may collectively point to an underlying adverse cause, combined with additional expert knowledge from the vaccine ontology, such as vaccine components, we will be able to understand the
root cause of different types of AEs. 1
William Beaumont Hospital Research Inst
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