Circulation, Vol 82, 872-878, Copyright © 1990 by American Heart Association
FG St.Goar, R Gibbons, I Schnittger, HA Valantine and RL Popp
In acute cardiac rejection, left ventricular diastolic function is altered,
and a restrictive ventricular filling pattern occurs. Doppler
echocardiographic indexes of mitral inflow have been proposed as sensitive
markers of the rejection process. As rejection progresses, the restrictive
ventricular filling pattern is reflected by a shortening of isovolumic
relaxation time and mitral valve pressure half- time and by an increase in
early transmitral filling velocity. Diastolic function is also compromised
in the nonrejecting cardiac transplant recipient during the early
postoperative period. This study examined the progression in
Doppler-derived mitral filling indexes in 25 recent cardiac transplant
recipients who demonstrated no histological evidence of transplant
rejection. Isovolumic relaxation time, mitral valve pressure half-time, and
early transmitral filling velocity were measured at postoperative weeks 1,
2, 4, and 6 on the day that surveillance right ventricular endomyocardial
biopsies were performed. The initial indexes were comparable to previously
described restrictive parameters and over the 6-week study period evolved
into a nonrestrictive filling pattern. This evolution reflects a
progressive improvement in postoperative diastolic function and a decrease
in left heart filling pressures. None of the evaluated clinical
characteristics, including preoperative pulmonary pressures, total ischemic
time of the transplanted heart, cardiopulmonary bypass time, and age of the
donor heart, correlated with this process. Given the increasing use of
Doppler echocardiography as a means of screening for transplant rejection,
it is important to have a thorough understanding of normal postoperative
changes in left ventricular diastolic function.
ARTICLES
Left ventricular diastolic function. Doppler echocardiographic changes soon after cardiac transplantation
Division of Cardiology, Stanford University School of Medicine, Calif. 94305.
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