Abstract |
A successful palliative arterial switch operation with arch repair in a 30-day-old infant with tricuspid atresia, ventriculoarterial discordance, subaortic stenosis, coarctation of the aorta, and aortic arch hypoplasia is reported. A concomitant Blalock-Taussig shunt was required because of insufficient pulmonary blood flow through the restrictive bulboventricular foramen. Postoperative arterial oxygen saturation was maintained around 90% and the pressure gradient between the left ventricle and the pulmonary artery was 45 mmHg according to a Doppler echocardiogram. The infant becomes free of subaortic stenosis and is awaiting the subsequent Fontan operation. This alternative palliative operation for neonates and early infants with double inlet ventricle, subaortic stenosis, and arch hypoplasia offers some advantages on the Fontan operation for avoiding pulmonary arterial distortion and subaortic stenosis followed by ventricular hypertrophy.
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Authors | M Yamagishi, K Nomura, S Kasahara, Y Nakamura |
Journal | [Zasshi] [Journal]. Nihon Kyobu Geka Gakkai
(Nihon Kyobu Geka Gakkai Zasshi)
Vol. 43
Issue 12
Pg. 1981-7
(Dec 1995)
ISSN: 0369-4739 [Print] Japan |
PMID | 8551084
(Publication Type: Case Reports, English Abstract, Journal Article)
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Topics |
- Aorta, Thoracic
(abnormalities, surgery)
- Aortic Coarctation
(complications)
- Aortic Valve Stenosis
(complications)
- Female
- Fontan Procedure
- Humans
- Infant, Newborn
- Palliative Care
- Transposition of Great Vessels
(complications)
- Tricuspid Atresia
(complications, surgery)
- Tricuspid Valve Insufficiency
(surgery)
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