Successful biventricular repair after initial Norwood operation for interrupted aortic arch with severe left ventricular outflow tract obstruction

Annals of Thoracic Surgery

Volumn 71, Issue 6, 2001, Pages 1974-1977

  Erez, Eldad ^a   Tam, Vincent K H ^a,b   Kanter, Kirk R ^a   Fyfe, Derek A ^a  

^a EMORY UNIVERSITY SCHOOL OF MEDICINE   (United States)

^b EMORY CLINIC   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

AORTA ARCH ANOMALY; ARTICLE; BALLOON DILATATION; CLINICAL ARTICLE; DISEASE SEVERITY; ECHOCARDIOGRAPHY; FOLLOW UP; HEART LEFT VENTRICLE OUTFLOW TRACT OBSTRUCTION; HUMAN; INFANT; NEWBORN; PRIORITY JOURNAL; SURGICAL TECHNIQUE;

AORTIC COARCTATION; FEMALE; FOLLOW-UP STUDIES; HEART VENTRICLES; HUMANS; INFANT; INFANT, NEWBORN; MALE; POSTOPERATIVE COMPLICATIONS; REOPERATION; SURVIVAL RATE; VENTRICULAR OUTFLOW OBSTRUCTION;

EID: 0034979731     PISSN: 00034975     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0003-4975(01)02591-7     Document Type: Article

References (19)

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8. Results of Norwood's operation for lesions other than hypoplastic left heart syndrome
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13. Survival in neonatal biventricular repair of left sided cardiac obstructive lesions associated with hypoplastic left ventricle
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15. The management of severe subaortic stenosis, ventricular septal defect, and aortic arch obstruction in the neonate
16. Biventricular repair for aortic atresia or hypoplasia and ventricular septal defect
17. Does left ventricular outflow tract obstruction influence outcome in interrupted aortic arch repair?
18. Early changes in ventricular geometry and ventricular septal defect size following Rastelli operation or intraventricular baffle repair for conotruncal anomaly: A cause for development of subaortic stenosis
19. The Philadelphia story: The 22q11.2 deletion: Report on 250 patients