CONAL ANATOMY IN 119 PATIENTS WITH D-LOOP TRANSPOSITION OF THE GREAT-ARTERIES AND VENTRICULAR SEPTAL-DEFECT - AN ECHOCARDIOGRAPHIC AND PATHOLOGICAL-STUDY
L. Pasquini et al., CONAL ANATOMY IN 119 PATIENTS WITH D-LOOP TRANSPOSITION OF THE GREAT-ARTERIES AND VENTRICULAR SEPTAL-DEFECT - AN ECHOCARDIOGRAPHIC AND PATHOLOGICAL-STUDY, Journal of the American College of Cardiology, 21(7), 1993, pp. 1712-1721
Objectives. We sought to study the range of conal morphology in transp
osition of the great arteries with ventricular septal defect and their
embryologic and surgical implications. Background. Conal anatomy in t
ransposition of the great arteries and ventricular septal defect is va
riable and might affect surgical repair. Methods. Conal anatomy was ex
plored using two-dimensional echocardiography in 119 patients with tra
nsposition of the great arteries and a large ventricular septal defect
who presented between 1984 and 1991. The influence of conal anatomy o
n surgical technique was determined by review of the operative reports
. Specimens of transposition of the great arteries with unusual conal
anatomy were selected from the Cardiac Registry for comparison with th
e echocardiograms. Results. One hundred five patients (88.2%) had suba
ortic conus only with no subpulmonary conus (Group 1). Subarterial con
us was present bilaterally in eight patients (6.7%) (Group 2). Four pa
tients (3.4%) had only subpulmonary conus with no (or minimal) subaort
ic conus (Group 3). Among these four patients, the aorta was posterior
to the pulmonary artery in one patient, side by side relative to the
pulmonary artery in two patients and slightly anterior in the fourth p
atient. Subarterial conus was absent bilaterally in two patients (1.7%
) (Group 4); the aorta was slightly posterior in one and side by side
with the pulmonary artery in the other. Conclusions. This variability
of conal anatomy in transposition of the great arteries with ventricul
ar septal defect implies four mechanisms by which transposition can oc
cur. The conal anatomy appeared to affect surgical repair in Groups 1
and 2 insofar as it influenced ventricular outflow tract obstruction.
In Groups 3 and 4, an arterial switch operation was performed in four
of the six patients. The posterior location of the aorta obviated the
need for the Lecompte maneuver in two of these four patients. In the r
emaining two cases in Groups 3 and 4, the condition was repaired by di
recting the left ventricular outflow across the ventricular septal def
ect to the aorta using a patch, with or without placement of a conduit
from the right ventricle to the pulmonary artery.