Contrast Media Clinical Trial
Official title:
Contrast Dynamics of the Thoracic Vasculature and Heart
In Contrast-Enhanced Magnetic Resonance Angiography (CE-MRA) a contrast agent is injected
into an arm vein using a programmable medical device called a power injector. Once the
contrast has circulated to the blood vessel of interest they can be imaged with MRI and
distinctly separated from surrounding non-vascular tissue.
This project is designed to find the best way to administer the contrast agent during CE-MRA
to produce the best images. The clinical availability of programmable power injectors
facilitates the use of variable contrast rate and volume injection protocols that are based
on patient specific parameters.
CE-MRA is a valuable imaging tool for diagnosing abnormalities of the major blood vessels in
the chest and abdomen. It is often used in conjunction with cardiac magnetic resonance (CMR)
examinations to evaluate the blood vessels of the heart and lung. CE-MRA is attractive
because 1) it does not involve radiation, and 2) the contrast agents used are not toxic to
the kidneys and can be used in patients who are at greater risk for kidney dysfunction
following iodinated contrast agents.
We plan to administer a small (1cc) test amount of contrast, taking pictures as the contrast
passes through the blood vessels, and analyze the results. Using this information, we will
administer an individually patient-tailored injection given in multiple phases (i.e., a
"multi-phasic" injection) to maintain constant contrast concentration (and therefore constant
signal intensity) throughout the scan. We believe this will reduce image blurring, and
improve the sharpness and likely the diagnostic quality of CE-MRA.
This project will build and validate a tool designed to optimize the use of magnetic
resonance (MR) contrast agents for contrast-enhanced magnetic resonance angiography (CE-MRA).
As with most angiography methods, contrast agents selectively highlight a patient's arteries
as compared to surrounding tissue. In CE-MRA the contrast agent is injected into an arm vein
using a programmable injector and transported by the body's circulation to the arteries of
interest, at which point a MR acquisition depicts the arteries distinctly from surrounding
soft tissue.
At present, the clinically accepted method of injecting the contrast agent is essentially the
same for every patient, and has not been systematically evaluated or optimized. For most
chest and abdominal CE-MRA studies contrast is injected over 5-15 seconds, and the resultant
concentration of contrast agent in the arteries over the duration of the MR acquisition is
not well known. What this concentration is and how it varies over time, however, has a large
impact on the quality and clarity of the resulting images. This project is designed to
optimize the concentration of contrast agent in the arteries during the MR scan by using the
predictive results of a small "test bolus" injection to tailor the actual contrast injection
for each individual patient such that concentration remains as high and as constant as
possible during the time of MR acquisition. This will be accomplished by developing
algorithms and software tools to tailor the optimal, patient-specific injection parameters.
The method will be validated in a preliminary clinical study.
We propose that we can predict what the contrast bolus will look like (i.e., its
"concentration vs. time") by first administering a small (1cc) test bolus, taking pictures as
the contrast passes through the blood vessels, and analyzing the results. Using this
information, we believe that an individually patient-tailored injection given in multiple
phases (i.e., a "multi-phasic" injection) can create constant contrast concentration (and
therefore constant signal intensity) throughout the scan, eliminating this source of image
blurring, and improving the sharpness and likely the diagnostic quality of first-pass CE-MRA.
Moreover, by tailoring the contrast to the duration of the scan, the contrast agent is used
most efficiently and not wasted outside the acquisition duration, potentially recouping any
contrast-to-noise ratio (CNR) loss. It is important to note the results of this study are
generalizable to CT Angiography (CTA) as well, where similar efficient use of the contrast
will reduce cost and excessive patient exposure to iodinated contrast. We plan to compare an
"optimized" multiphasic contrast administration to a standard single phase contrast
administration.
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