Assessment of Cardiac Allograft Vasculopathy With Optical Coherence Tomography



Status:Completed
Conditions:Cardiology
Therapuetic Areas:Cardiology / Vascular Diseases
Healthy:No
Age Range:18 - Any
Updated:5/5/2014
Start Date:August 2011
End Date:August 2013
Contact:Rebecca E Nelson
Email:nelson.rebecca@mayo.edu
Phone:507-288-8388

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Assessment of Cardiac Allograft Vasculopathy With Optical Coherence Tomography as Compared to Intravascular Ultrasound-Virtual Histology

Cardiac allograft vasculopathy (CAV) is a progressive disease of the coronary arteries in
transplanted hearts which is a significant cause of morbidity and mortality. The broad
objective of this research study is to advance our ability to diagnose as early as possible
the presence of CAV and to non-invasively predict those patients at increased risk of CAV
with novel techniques. Optical coherence tomography (OCT) is a novel intracoronary imaging
technique using an optical analog of ultrasound with a resolution 10 times greater
resolution than intravascular ultrasound (IVUS). Endothelial progenitor cells (EPCs) in
peripheral blood have been shown to play a role in the pathogenesis of atherosclerosis and
peripheral arterial tonometry is a clinical tool used to predict endothelial dysfunction (a
precursor of atherosclerosis) which has been validated in non-transplant patients. Patients
scheduled for routine cardiac catheterization with IVUS at the Mayo Clinic Rochester, MN
that reach inclusion and exclusion criteria for the study will be approached on the day to
get informed consent to perform OCT, blood sampling and peripheral endothelial function
testing. The investigators aim to 1) compare the frequency and plaque type of CAV as defined
with OCT versus IVUS-Virtual Histology (IVUS-VH), 2) predict the presence and severity of
CAV with absolute counts of EPCs and 3) with peripheral endothelial function scores.


Inclusion Criteria:

- patients aged 18 or older

- patients with cardiac transplant undergoing routine CAV surveillance

Exclusion Criteria:

- patients < 18 years old

- patients with acute rejection

- patients with active infection

- patients with chronic renal insufficiency with a GFR < 30ml/min

- patients not able to give informed consent
We found this trial at
1
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200 First Street SW
Rochester, Minnesota 55905
507-284-2511
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