Drop-of-blood technology for diagnosis and therapeutic drug monitoring in patients with infectious disease
Project Number5R21EB031401-03
Former Number1R21EB031401-01
Contact PI/Project LeaderKHISMATULLIN, DAMIR B
Awardee OrganizationTULANE UNIVERSITY OF LOUISIANA
Description
Abstract Text
PROJECT SUMMARY
The COVID-19 pandemic took lives of more than 2.5 million people globally including more than 500 thousand in the
United States in one year. Many deaths occurred after rapid health deterioration, shortly after symptoms of the disease were
manifested. Clinical evidence collected from patients with severe disease indicates that this deterioration occurred because
of the cytokine storm and resulting activation of the coagulation system, leading to uncontrolled thrombotic events in
pulmonary microvasculature and throughout the body. Similar to COVID-19, severe complications of other infectious
diseases are known to be associated with coagulation abnormalities causing disseminated intravascular coagulation, venous
thromboembolism, arterial thrombosis, or ischemic stroke. High levels of D-dimer, the test for hyperactive coagulation
system, were found to be correlated with high mortality in patients with infectious disease including COVID-19. Many of
these patients could be saved if they were properly and timely treated based on infectious disease risk assessment. However,
tests that effectively predict the severity of infectious diseases are not available yet.
The objective of this proposal is to develop a drop-of-blood test for rapid point-of-care assessment of infectious disease
severity, based on integrated quasi-static acoustic tweezing thromboelastometry (i-QATT). In this unique approach,
comprehensive coagulation analysis is done without inducing blood sample contact with artificial surfaces and by using a
single drop of blood, which volume (4-6 microliters) is nearly 100 times less the minimal sample volume currently required
for coagulation tests. For rapid assessment of infectious disease risk inside a hospital or under outpatient settings, we propose
to use this method on venous blood samples or finger prick capillary blood samples. We hypothesize that 1) i-QATT
capillary blood analysis can detect coagulation abnormalities, 2) severe complications from infectious diseases develop due
to cytokine storm-induced activation of the coagulation system, and 3) severity of infectious diseases can be assessed from
blood coagulation analysis. The technology development for infectious disease severity assessment and testing the above
hypotheses will be achieved via the following specific aims: 1) establish and standardize the acoustic tweezing technology
for coagulation measurements of capillary blood, 2) assess changes in the coagulation system induced by cytokine storm
via drop-of-blood measurements, and 3) test the feasibility of drop-of-blood acoustic tweezing technology for infectious
disease severity assessment.
Public Health Relevance Statement
PROJECT NARRATIVE
The COVID-19 pandemic that took lives of more than 500,000 U.S. citizens is the evidence that emerging infectious
diseases are a serious threat to human health. Many patients who died from COVID-19 and other infectious diseases
developed severe thrombotic complications shortly after disease symptoms were manifested, and their lives could be
saved by predictive diagnosis of disease severity and timely treatment. The goal of the proposed research is develop
technology for infectious disease severe assessment that requires only a single drop of venous or capillary blood and can
be performed inside a hospital, in a clinic or outpatient center, or at home.
National Institute of Biomedical Imaging and Bioengineering
CFDA Code
286
DUNS Number
053785812
UEI
XNY5ULPU8EN6
Project Start Date
15-July-2022
Project End Date
30-April-2025
Budget Start Date
01-May-2024
Budget End Date
30-April-2025
Project Funding Information for 2024
Total Funding
$190,000
Direct Costs
$125,000
Indirect Costs
$65,000
Year
Funding IC
FY Total Cost by IC
2024
National Institute of Biomedical Imaging and Bioengineering
$190,000
Year
Funding IC
FY Total Cost by IC
Sub Projects
No Sub Projects information available for 5R21EB031401-03
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