The goal of this research is to develop a new method of intravascular imaging, which has the possibility of identifying atherosclerotic lesions. The lesions would then be characterized as to their potential for progression to alteration or rupture. The possibility of identifying and discriminating those lesions which are at risk for rupture has great significance. The applicants proposed to use optical coherence tomography (OCT) to develop a high resolution intravascular imaging system for the diagnosis of atherosclerotic lesions. The applicants noted the analogy of OCT to B Mode ultrasound imaging. However, the use of infrared light rather than acoustical waves should provide high resolution, broad dynamic range, and easy integration into cardiovascular catheter systems. The principal focus of this application is the development of background feasibility experiments designed to assess the feasibility of this approach. These background experiments focus on identifying advantages and limitations of OCT for intravascular imaging and maximizing performance.
The specific aims are: 1) To perform imaging on a wide range of plaque morphologies and vascular components; 2) To determine the limitations associated with imaging through whole blood; 3) To identify the optimal incident wavelength for OCT imaging of the vasculature; 4) To directly compare the ability of both OCT and high frequency ultrasound (IVUS) to assess micropathology within human atherosclerotic plague in virtu; and 5) To demonstrate the ability of OCT and IVUS to perform in vivo imaging of an intravascular stent within a rabbit aorta.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
First Independent Research Support & Transition (FIRST) Awards (R29)
Project #
5R29HL055686-04
Application #
6043888
Study Section
Special Emphasis Panel (ZRG7-DMG (01))
Project Start
1996-08-01
Project End
2000-03-25
Budget Start
1999-08-01
Budget End
2000-03-25
Support Year
4
Fiscal Year
1999
Total Cost
Indirect Cost
Name
Massachusetts General Hospital
Department
Type
DUNS #
City
Boston
State
MA
Country
United States
Zip Code
02199
Brezinski, Mark E; Harjai, Kishore J (2014) Longitudinal necrotic shafts near TCFAs--a potential novel mechanism for plaque rupture to trigger ACS? Int J Cardiol 177:738-41
Giattina, Susanne D; Courtney, Brian K; Herz, Paul R et al. (2006) Assessment of coronary plaque collagen with polarization sensitive optical coherence tomography (PS-OCT). Int J Cardiol 107:400-9
Stamper, Debra; Weissman, Neil J; Brezinski, Mark (2006) Plaque characterization with optical coherence tomography. J Am Coll Cardiol 47:C69-79
Rogowska, J; Patel, N; Plummer, S et al. (2006) Quantitative optical coherence tomographic elastography: method for assessing arterial mechanical properties. Br J Radiol 79:707-11
Brezinski, Mark E (2006) Optical coherence tomography for identifying unstable coronary plaque. Int J Cardiol 107:154-65
Patel, Nirlep A; Zoeller, Jason; Stamper, Debra L et al. (2005) Monitoring osteoarthritis in the rat model using optical coherence tomography. IEEE Trans Med Imaging 24:155-9
Li, Xingde; Martin, Scott; Pitris, Costas et al. (2005) High-resolution optical coherence tomographic imaging of osteoarthritic cartilage during open knee surgery. Arthritis Res Ther 7:R318-23
Rogowska, Jadwiga; Bryant, Clifford M; Brezinski, Mark E (2003) Cartilage thickness measurements from optical coherence tomography. J Opt Soc Am A Opt Image Sci Vis 20:357-67
Patel, Nirlep A; Li, Xingde; Stamper, Debra L et al. (2003) Guidance of aortic ablation using optical coherence tomography. Int J Cardiovasc Imaging 19:171-8
Martin, S D; Patel, N A; Adams Jr, S B et al. (2003) New technology for assessing microstructural components of tendons and ligaments. Int Orthop 27:184-9

Showing the most recent 10 out of 33 publications