TY - JOUR
T1 - Parameterization of left ventricular wall motion for detection of regional ischemia
AU - Herz, Susan L.
AU - Ingrassia, Christopher M.
AU - Homma, Shunichi
AU - Costa, Kevin D.
AU - Holmes, Jeffrey W.
N1 - Funding Information:
This work was funded by National Science Foundation grant BES-02-01617 (PI JWH, Co-PI KDC). SLH was supported by a Louis Morin Fellowship. Dr. Andrew McCulloch at the University of California, San Diego, provided the finite element software Continuity through the National Biomedical Computation Resource (NIH P41RR08605). In addition, the authors thank Drs. Todd Pulerwitz (Medicine) and Elsa Angelini (Biomedical Engineering) for their ideas and input regarding this project.
PY - 2005/7
Y1 - 2005/7
N2 - While qualitative wall motion analysis has proven valuable in clinical cardiology practice, quantitative analyses remain too time-consuming for routine clinical use. Our long-term goal is therefore to develop automated methods for quantitative wall motion analysis. In this paper, we utilize a finite element model of the regionally ischemic canine left ventricle to demonstrate a new approach based on parameterization of the left ventricular endocardial surface in prolate spheroidal coordinates. The parameterization provided a substantial data reduction and enabled simple definition, calculation, and display of three-dimensional fractional shortening (3DFS), a quantitative measure of wall motion analogous to the fractional shortening measure used in 2D analysis. The endocardial surface area displaying akinesis or dyskinesis by 3DFS corresponded closely to simulated ischemic region size and 3DFS identified appropriate wall motion abnormalities during experimental coronary occlusion in a canine pilot study. 3DFS therefore appears to be a reasonable candidate for clinical tests to determine its utility in identifying and quantifying acute regional ischemia in patients. By linking state of the art finite element models to the clinically relevant framework of wall motion analysis, the methods presented here will facilitate formulation, in silico prescreening, and clinical testing of additional candidate measures of wall motion.
AB - While qualitative wall motion analysis has proven valuable in clinical cardiology practice, quantitative analyses remain too time-consuming for routine clinical use. Our long-term goal is therefore to develop automated methods for quantitative wall motion analysis. In this paper, we utilize a finite element model of the regionally ischemic canine left ventricle to demonstrate a new approach based on parameterization of the left ventricular endocardial surface in prolate spheroidal coordinates. The parameterization provided a substantial data reduction and enabled simple definition, calculation, and display of three-dimensional fractional shortening (3DFS), a quantitative measure of wall motion analogous to the fractional shortening measure used in 2D analysis. The endocardial surface area displaying akinesis or dyskinesis by 3DFS corresponded closely to simulated ischemic region size and 3DFS identified appropriate wall motion abnormalities during experimental coronary occlusion in a canine pilot study. 3DFS therefore appears to be a reasonable candidate for clinical tests to determine its utility in identifying and quantifying acute regional ischemia in patients. By linking state of the art finite element models to the clinically relevant framework of wall motion analysis, the methods presented here will facilitate formulation, in silico prescreening, and clinical testing of additional candidate measures of wall motion.
KW - Cardiac mechanics
KW - Computer models
KW - Finite element
KW - Prolate spheroidal coordinates
KW - Stress echocardiography
KW - Ultrasound
UR - http://www.scopus.com/inward/record.url?scp=22344441328&partnerID=8YFLogxK
U2 - 10.1007/s10439-005-3312-7
DO - 10.1007/s10439-005-3312-7
M3 - Article
C2 - 16060531
AN - SCOPUS:22344441328
SN - 0090-6964
VL - 33
SP - 912
EP - 919
JO - Annals of Biomedical Engineering
JF - Annals of Biomedical Engineering
IS - 7
ER -