Open AccessGlobal left ventricular function and regional wall motion in pure mitral stenosis‐Left ventricular function in pure mitral stenosis
Author(s) -
Colle J. P.,
Rahal S.,
Ohayon J.,
Bonnet J.,
Le Goff G.,
Besse P.,
Bricaud H.
Publication year - 1984
Publication title -
clinical cardiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.263
H-Index - 72
eISSN - 1932-8737
pISSN - 0160-9289
DOI - 10.1002/clc.4960071103
Subject(s) - medicine , ventricle , cardiology , ejection fraction , stenosis , diastole , contraction (grammar) , cardiac cycle , systole , mitral valve , blood pressure , heart failure
Global left ventricular function (LVF) and scgmental wall motion of the left ventricle are registered in 113 patients presenting a pure mitral stenosis (MS) and in a control group of 50 individuals. The segmental wall motion is measured on the end‐diastolic‐end‐systolic frames of the left ventricle, obtained from right anterior oblique (RAO) monoplane cineangiography. Measurement of the segmental wall shortening is performed using the Stanford method. Group 1 includes 68 patients (60% of the total number of patients studied). These patients show no pathological contraction abnormality. In this group, the global LVF is not different from the control group. Group 2 includes 45 patients (40% of the total) for whom contraction abnormalities are present: anterior hypokinesis in 20% of the cases (anterior area mean shortening (AAS) = 18±8%; p<0.001 vs. group 1 and control group), and posterior hypokinesis in 20% of the cases (posterior area mean shortening (PAS) = 9.8 ±5.8%, p<0.001 vs. group 1 and control group). In this group, global LVF is impaired; ejection fraction (EF) = 0.57±0.1% (p<0.001 vs. group 1); velocity of circumferential fiber shortening (Vcf) = l±0.3 circ/s (p<0.001 vs. group 1); end‐diastolic pressure (EDP) = 11±5 mmHg (p<0.01 vs. group 1). Segmental contraction abnormalities appear to be the main factor involved in the global LVF impairment. Segmental wall motion abnormalities could be related to subvalvular fibrosis, or LV filling difficulties, or principally, to a possible interplay between the right and the left ventricles.