Venous thromboembolism (VTE) manifests as deep vein thrombosis (DVT) of the leg and its complication, pulmonary embolism (PE). VTE is a major health problem with over 400,000 VTE events in the US annually. VTE costs more than $8 billion per year to our health care system and causes more than 100,000 deaths per year in the US alone. Despite administration of chemoprophylaxis to trauma patients during hospitalization, about 5% of patients still develop symptomatic VTE prior to discharge and more alarmingly, about 40-60% of patients develop symptomatic VTE after discharge. Hence, we need a personalized and individualized VTE risk score for acutely injured patients and to address the NIH initiative of defining the ?role of laboratory monitoring? to help better define those at risk of bleeding and thrombosis.? Our specific aims will address current gaps in knowledge by:
(Aim 1) validation of a VTE risk prediction tool for the individual with acute trauma using clinical data, novel plasma biomarkers, and (Aim 2) to assess if addition of genotype data (i.e., F5 rs6025 [Factor V Leiden], F2 rs1799963 [Prothrombin G20210A], and ABO rs8176719 [non-O blood type]) improve the accuracy of the prediction tool. Successful completion of our study aims will provide a validated, generalizable, clinically-applicable risk assessment tool for stratifying risk of VTE in the individual trauma patient. This risk tool, which incorporates easily obtainable clinical risk factors, as well as the individual patient's prothrombotic phenotype and genotype, will more accurately predict the occurrence of symptomatic VTE after injury.

Public Health Relevance

Relevance Almost one-half million people suffer venous thromboembolism annually in the United States, and one-third die from this disease. Massive bleeding from injury accounts for half of early deaths after trauma. This study aims to prevent the deaths and suffering associated with venous thromboembolism and bleeding by identifying the individual person at high risk of these complications in order to take preventive measures.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
5R01GM126086-03
Application #
9942485
Study Section
Special Emphasis Panel (ZRG1)
Program Officer
Zhao, Xiaoli
Project Start
2018-09-05
Project End
2023-05-31
Budget Start
2020-06-01
Budget End
2021-05-31
Support Year
3
Fiscal Year
2020
Total Cost
Indirect Cost
Name
Mayo Clinic, Rochester
Department
Type
DUNS #
006471700
City
Rochester
State
MN
Country
United States
Zip Code
55905