Jh. Gorman et al., DYNAMIC 3-DIMENSIONAL IMAGING OF THE MITRAL-VALVE AND LEFT-VENTRICLE BY RAPID SONOMICROMETRY ARRAY LOCALIZATION, Journal of thoracic and cardiovascular surgery, 112(3), 1996, pp. 712-725
Objectives, The first objective was to develop a quantitative method f
or tracking the three-dimensional geometry of the mitral valve, The se
cond was to determine the complex interrelationships of various compon
ents of the mitral valve in vivo. Methods and results. Sixteen sonomic
rometry transducers were placed around the mitral valve anulus, at the
tips and bases of both papillary muscles, at the ventricular apex, ac
ross the ventricular epicardial short axis, and on the anterior chest
wall before and during cardiopulmonary bypass in eight anesthetized sh
eep, Animals were studied later on 17 occasions, Reproducibility of de
rived chord lengths and three-dimensional coordinates from sonomicrome
try array localization, longevity of transducer signals, and the dynam
ics of the mitral valve and left ventricle were studied, Reproducibili
ty of distance measurements averages 1.6%; Procrustes analysis of thre
e-dimensional arrays of coordinate locations predicts an average error
of 2.2 mm, Duration of serial sonomicrometry array localization signa
ls ranges between 60 and 151 days (mean 114 days), Sonomicrometry arra
y localization demonstrates the saddle-shaped mitral anulus, its minim
al orifice area immediately before end-diastole, and uneven, apical de
scent during systole, Papillary muscles shorten only 3.0 to 3.5 mm, So
nomicrometry array localization demonstrates nonuniform torsion of pap
illary muscle transducers around a longitudinal axis and shows rotatio
n of papillary muscular bases toward each other during systole, Conclu
sion. Tagging of ventricular structures in experimental animals by son
omicrometry array localization images is highly reproducible and suita
ble for serial observations, In sheep the method provides unique, quan
titative information regarding the interrelationship of mitral valvula
r and left ventricular structures throughout the cardiac cycle.