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Completed NON-SBIR/STTR RPGS NIH (US)

Incorporation of multilevel ontologies of adverse events and vaccines for vaccine safety surveillance

$3.75M USD

Funder NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES
Recipient Organization University of Michigan At Ann Arbor
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 10174317
Grant Description

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

All Grantees

University of Michigan At Ann Arbor

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