Cardiovascular Journal of Africa: Vol 23 No 2 (March 2012) - page 76

CARDIOVASCULAR JOURNAL OF AFRICA • Vol 23, No 2, March 2012
e10
AFRICA
genous flap from the pulmonary artery decreases the risk of
reoperation in the future.
The main disadvantage of this technique is the necessity for
a non-hypoplastic main pulmonary artery. Continuity between
the right ventriculotomy and the main pulmonary artery was
achieved through the flap produced from the main pulmonary
artery. Therefore the posterior wall of the main pulmonary artery
must be preserved for the integrity of the artery. This will ensure
sewing of the pericardial patch to both pulmonary arteries (the
flap and the
in-situ
posterior pulmonary artery).
In long-term follow up of TOF operations, intractable malign
arrhythmias and pulmonary insufficiency leading to right
ventricular dysfunction are the main problems that surgeons
face. Although the follow up in our patients was not long enough,
we detected pulmonary insufficiency in the short term. However,
we did not observe right ventricular dysfunction or arrhythmia in
any of our patients.
Conclusion
The ‘double-outflow’ technique is appropriate for TOF patients
with coronary artery anomalies, since it is easy to perform, has
no additional cost or the need for a conduit. The technique has
highly favorable outcomes; reoperation rates are low due to the
use of a tissue conduit which has the potential to grow. The tech-
nique can be applied to infants, so they are protected from the
deleterious effects of hypoxia.
References
1.
Humes RA, Driscoll JD, Danielson GK,
et al
. Tetralogy of Fallot
with anomalous origin of the left anterior descending artery: surgical
options.
J Thorac Cardiovasc Surg
1987;
94
: 784– 787.
2.
Klara S, Sharma R, Choudhary SK
et al.
Right ventricular outflow tract
after non-conduit repair of tetralogy of Fallot with coronary anomaly.
Ann Thorac Surg
2000;
70
(3): 723–726.
3.
Daskalopoulos DA, Edwards WD, Driscoll DJ,
et al.
Coronary artery
compression with fatal myocardial ischemia. A rare complication of
valved extracardiac conduits in children with congenital heart disease.
J Thorac Cardiovasc Surg
1983;
85
(4): 546–551.
4.
Van Son JA. Repair of tetralogy of Fallot with anomalous origin of left
anterior descending coronary artery.
J Thorac Cardiovasc Surg
1995;
110
(2): 561–562.
5.
Asano M, Saito T, Nomura N, Mishima A. Double-outlet technique
for tetralogy of Fallot-type disease with an anomalous coronary artery.
Pediatr Cardiol
2005;
26
(5): 710–712.
6.
Dandolu BR, Baldwin HS, Norwood WI Jr., Jacobs ML. Tetralogy of
Fallot with anomalous coronary artery: double outflow technique.
Ann
Thorac Surg
2000;
67
(4): 1178–1180.
7.
Dabizzi RP, Caprioli G, Aiazzi L,
et al
. Distribution and anomalies
of coronary arteries in tetralogy of Fallot.
Circulation
1980;
61
(1):
95–102.
8.
Omay O, Vuran AC, Gönen H,
et al
. Double-outlet technique for tetral-
ogy of Fallot-type diseases with an anomalous coronary artery: case
report. Turkish Clinics.
J Cardiovasc Sci
2010;
22
(2): 266–269.
9.
Cobanoglu A, Schultz JM. Total correction of tetralogy of Fallot in the
first year of life: Late results.
Ann Thorac Surg
2002;
74
: 133–138.
10. Pigula FA, Khalil PN, Mayer JE,
et al.
Repair of tetralogy of Fallot in
neonates and young infants.
Circulation
1999;
100
(19 suppl): 157–161.
1...,66,67,68,69,70,71,72,73,74,75 77,78,79,80
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