DYNAMICS OF MITRAL REGURGITANT FLOW AND ORIFICE AREA - PHYSIOLOGICAL APPLICATION OF THE PROXIMAL FLOW CONVERGENCE METHOD - CLINICAL-DATA AND EXPERIMENTAL TESTING
E. Schwammenthal et al., DYNAMICS OF MITRAL REGURGITANT FLOW AND ORIFICE AREA - PHYSIOLOGICAL APPLICATION OF THE PROXIMAL FLOW CONVERGENCE METHOD - CLINICAL-DATA AND EXPERIMENTAL TESTING, Circulation, 90(1), 1994, pp. 307-322
Background The proximal how convergence method, a quantitative color D
oppler flow technique, has been validated recently for calculating reg
urgitant flow and orifice area. We investigated the potential of the m
ethod as a tool to study different pathophysiological mechanisms of mi
tral valve incompetence by assessing the time course of regurgitant fl
ow and orifice area and analyzed the implications for quantification o
f mitral regurgitation. Methods and Results Fifty-six consecutive pati
ents with mitral regurgitation of different etiologies were studied. T
he instantaneous regurgitant flow rate Q((t)) was computed from color
M-mode recordings of the proximal flow convergence region and divided
by the corresponding orifice velocity V-(t) to obtain the instantaneou
s orifice area A((t)). Regurgitant stroke volume (RSV) was obtained by
integrating Q((t)). Mean regurgitant flow rate Qm( )was calculated by
RSV divided by regurgitation time. Peak-to-mean regurgitant flow rate
s Q(p)/Q(m) and orifice areas A(p)/A(m) were calculated to assess the
phasic character of Q((t)) and P-(t) In the first 24 patients (group 1
), computation of Q(m) and RSV from the color Doppler recordings was c
ompared with the conventional pulsed Doppler method (r=.94, SEE=29.4 m
L/s and r=.95, SEE=9.7 mL) as well as with angiography (r(s)=.93 and r
(s)=.94, P<.001). The temporal variation of Q((t)) and A((t)) was stud
ied in the next 32 patients (group 2): In functional regurgitation in
dilated cardiomyopathy (n=12), there was a constant decrease in A((t))
throughout systole with an increase during left ventricular relaxatio
n; A(p)/A(m) was 5.49+/-3.17. In mitral valve prolapse (n=6), A((t)) w
as small in early systole, increasing substantially in midsystole, and
decreasing mildly during left ventricular relaxation; A(p)/A(m) was 2
.48+/-0.26. In rheumatic mitral regurgitation (n=14), a roughly consta
nt regurgitant orifice area during most of systole was found in 4 pati
ents. In the other patients there was significant variation of A((t))
and the time of its maximum; A(p)/A(m) was 1.81+/-0.56. ANOVA demonstr
ated that the differences in A(p)/A(m) were related to the etiology of
mitral regurgitation (P<.0001). To verify that the calculated variati
on in regurgitant orifice area during the cardiac cycle reflects an ac
tual variation, the ability of the method to predict a constant orific
e area throughout systole was tested experimentally in a canine model
of mitral regurgitation. Five flow stages were produced by implanting
fixed grommet orifices of different sizes into the anterior mitral lea
flet. A constant regurgitant orifice area was correctly predicted thro
ughout systole with a mean percent error of -1.8+/-4% (from -6.9% to 5.8%); the standard deviation of the individual curves calculated at 1
0% intervals during systole averaged 13.3% (from 3.6% to 19.6%). In ad
dition, functional mitral regurgitation caused by ventricular dysfunct
ion was produced pharmacologically in five dogs, and the color M-mode
recordings of the proximal flow convergence region were obtained with
the transducer placed directly on the heart instead of the chest, thus
ruling out a significant effect of translational motion on the observ
ed flow pattern. The pattern of regurgitant how variation was identica
l to that observed in patients. Conclusions The proximal flow converge
nce method demonstrates that regurgitant flow and orifice area vary th
roughout systole in distinct patterns characteristic of the underlying
mechanism of mitral incompetence. Therefore, in addition to the poten
tial of the method as a tool to quantify mitral regurgitation, it allo
ws analysis of the pathophysiology of regurgitation in the individual
patient, which may be helpful in clinical decision making. Calculating
mitral regurgitant flow rate and volume from the time-varying proxima
l how field tie, without assuming a constant orifice area that would p
roduce overestimation in individual patients) provides excellent agree
ment with independent techniques and agrees well with angiography.