R. Mazhari et al., REGIONAL MYOCARDIAL PERFUSION AND MECHANICS - A MODEL-BASED METHOD OFANALYSIS, Annals of biomedical engineering, 26(5), 1998, pp. 743-755
A new parametric model-based method has been developed that allows epi
cardial strain distributions to be computed on the left ventricular fr
ee wall in normal and ischemic myocardium and integrated with the regi
onal distributions of anatomic and physiological measurements so that
underlying relationships can be explored. An array of radiopaque marke
rs was sewn on the anterior wall of the left ventricle (LV) in three a
nesthetized open-chest canines, and their positions were recorded usin
g biplane video fluoroscopy before and 2 min after occlusion of the le
ft anterior descending coronary artery. The three-dimensional (3D) ana
tomy of the LV and epicardial fiber angles were measured post-mortem u
sing a 3D probe. A prolate spheroidal finite element model was fitted
to the epicardial surface points (with <0.2 mm accuracy) and fiber ang
les (<5 degrees error). Regional myocardial blood flows (MBFs) were me
asured using fluorescent microspheres and fitted into the model (<0.3
ml min(-1) g(-1) error). Epicardial fiber and cross-fiber strain distr
ibutions were computed by allowing the model to deform from end-diasto
le to end-systole according to the recorded motion of the surface mark
ers. Systolic fiber strain varied from -0.05 to 0.01 within the region
of the markers during baseline, and regional MBF varied from 1.5 to 2
.0 ml min(-1) g(-1). During 2 min ischemia, regional MBF was less than
0.3 ml min(-1) g(-1) in the ischemic region and 1.0 ml min(-1) g(-1)
in the nonischemic region, and fiber strain ranged from 0.05 in the ce
ntral ischemic zone to - 0.025 in the remote nonischemic tissue. This
analysis revealed a zone of impaired fiber shortening extending into t
he normally perfused myocardium that was significantly wider at the ba
se than the apex. A validation analysis showed that a regularizing fun
ction can be optimized to minimize both fitting errors and numerical o
scillations in the computed strain fields. (C) 1998 Biomedical Enginee
ring Society. [S0090-6964(98)01505-7].