Mh. Yacoub et al., ANATOMIC CORRECTION OF THE SYNDROME OF PROLAPSING RIGHT CORONARY AORTIC CUSP, DILATATION OF THE SINUS OF VALSALVA, AND VENTRICULAR SEPTAL-DEFECT, Journal of thoracic and cardiovascular surgery, 113(2), 1997, pp. 253-260
Background: Although the syndrome of ventricular septal defect and aor
tic regurgitation was described a long time ago, there is still no agr
eement about the anatomic and functional components of the syndrome an
d the optimal methods of management, Objective: Our objective was to d
escribe a new simple technique of anatomic correction of all the compo
nents of the syndrome, based on redefining the salient anatomic and fu
nctional features of the syndrome, Methods: Anatomic correction of the
syndrome is achieved through a transaortic approach with the placemen
t of a series of pledget-supported mattress sutures using autogenous p
ericardium, The sutures are used to close the ventricular septal defec
t, plicate the aortic sinus, and correct the outward and downward disp
lacement of the anulus of the aortic valve, The technique is designed
to correct all the anatomic functional components including severe aor
tic regurgitation when present, Results: Between 1972 and 1996, 46 pat
ients with this syndrome underwent surgical treatment, The current tec
hnique was used in most of the patients operated on before 1981 and in
all patients since that date, There were no early or late deaths duri
ng a follow-up period varying from 3 months to 24 years (mean 8.4 year
s), Aortic regurgitation was abolished in 16 and improved in the remai
ning patients, The hemodynamic results have been maintained except in
five patients operated on early in the series, in whom additional proc
edures on the cusps were performed, Conclusions: Anatomic correction o
f all the components of the syndrome of prolapsing right coronary cusp
, dilatation of the sinus of Valsalva, and ventricular septal defect,
can be achieved by a very simple technique, This technique can be appl
ied in young children and prevents progression and secondary changes,
Early correction in all patients with this syndrome is warranted.