ONE STAGE REPAIR OF AORTIC-ARCH ANOMALIES AND INTRACARDIAC DEFECTS

被引:26
作者
HAZEKAMP, MG
QUAEGEBEUR, JM
SINGH, S
HARDJOWIJONO, R
BOGERS, AJJC
OTTENKAMP, J
ROHMER, J
WITSENBURG, M
HESS, J
BOS, E
HUYSMANS, HA
机构
[1] Departments of Cardiothoracic Surgery and Pediatric Cardiology, University Hospital Rotterdam, Rotterdam
[2] Departments of Cardiothoracic Surgery and Pediatric Cardiology, University Hospital, Leiden
[3] Departments of Cardiothoracic Surgery and Pediatric Cardiology, University Hospital, Leiden
[4] Departments of Cardiothoracic Surgery and Pediatric Cardiology, University Hospital Rotterdam, Rotterdam
关键词
CONGENITAL HEART DISEASE; INTERRUPTED AORTIC ARCH; COARCTATION; CARDIAC SURGERY; ONE STAGE REPAIR;
D O I
10.1016/1010-7940(91)90036-J
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Between August 1985 and May 1990, 27 neonates and infants underwent combined correction of intracardiac and aortic arch anomalies through a median sternotomy. Coarctation (CoA) was combined with VSD (6), AVSD (2), Taussig-Bing (TB) heart (5), transposition of the great arteries (TGA) (1), TGA + VSD (2), congenitally corrected TGA + VSD (1) and VSD + myxoid stenotic outlet valves (1). Interrupted aortic arch (IAA) was combined with VSD (10) and TB heart (1). Two patients had IAA type B as well as CoA. Age at operation varied from 2 to 243 days with a mean age of 51 days. Twenty patients (70%) were younger than 30 days. One TGA + VSD and all TB hearts had malaligned outlet septum and right ventricular outflow tract obstruction (RVOTO). Posterior outlet septum deviation and left ventricular outflow tract obstruction (LVOTO) occurred in 8 patients with malalignment VSD and IAA (7) or CoA (1). Aortic arch reconstruction was performed using extended end-to-end anastomoses. In 3 patients, arch hypoplasia necessitated patch implantation. VSDs were closed through the right atrium unless the anatomy dictated otherwise. One TB heart was reconstructed with a Kawashima procedure. All other TB hearts and all TGAs were corrected with arterial switch operation. Obstructing outlet septum was resected whenever necessary. Follow-up was complete and included echo-Doppler control. Eleven patients had postoperative heart catheterisation. Early mortality was 18.5% (5 patients). Persisting LVOTO or RVOTO was responsible. There was no late mortality. Five patients were reoperated upon: 3 for stenotic anastomoses and 2 for a subaortic membranous stenosis. Successful balloon dilatation of recoarctation was performed four times. Two patients with malaligned septum remain with significant LVOTO. Final results are good in the other 20 patients. One stage repair gives good results and will benefit the patient in the immediate postoperative course as well as in its further development. RVOTO in TB anomaly or TGA must be carefully corrected. Persisting LVOTO continues to be a major problem in patients with malalignment VSD.
引用
收藏
页码:283 / 287
页数:5
相关论文
共 19 条
[1]  
Baratt-Boyes B.G., Nicholls T.T., Brandt P., Neutze J.M., Aortic arch interruption associated with patent ductus arteriosus, ventricular septal defect, and total anomalous pulmonary venous connection: Total correction in an 8-day old infant by means of profound hypothermia and limited cardiopulmonary bypass, J Thorac Cardiovasc Surg, 63, pp. 367-373, (1972)
[2]  
Braunlin E.A., Lock J.E., Foker J.E., Repair of type B interruption of the aortic arch, J Thorac Cardiovasc Surg, 86, pp. 920-925, (1983)
[3]  
Fishman N.H., Bronstein M.H., Berman W., Roe B.B., Edmunds L.H., Robinson S.J., Rudolph A.M., Surgical management of severe aortic coarctation and interrupted aortic arch in neonates, J Thorac Cardiovasc Sing, 71, pp. 35-48, (1976)
[4]  
Hammon J.W., Merrill W.H., Prager R.L., Graham T.P., Bender H.W., Repair of interrupted aortic arch and associated malformations in infancy: Indications for complete or partial repair, Ann Thorac Surg, 42, pp. 17-21, (1986)
[5]  
Kanter K., Erson R.H., Lincoln C., Rigby M.L., Shineboum E.A., Anatomic correction for complete transposition and double outlet right ventricle, J Thorac Cardiovasc Surg, 90, pp. 690-699, (1985)
[6]  
Kirklin J.K., Blackstone E.M., Kirklin J.W., McKay R., Pacifico A.D., Bargeron L.M., Intracardiac surgery in infants under age 3 months: Incremental risk factors for hospital mortality, Am J Cardiol, 48, pp. 500-506, (1981)
[7]  
Kron I.L., Rheuban K.S., Carpenter M.S., Nolan S.P., Interrupted aortic arch: A conservative approach for the sick neonate, J Thorac Cardiovasc Surg, 86, pp. 37-40, (1983)
[8]  
Leoni F., Hukta J.C., Douglas J., McKay R., Deleval M.R., McCartney F.J., Stark J., Effect of prostaglandin on surgical mortality in obstructive lesions of the systemic circulation, Br Heart J, 52, pp. 654-659, (1984)
[9]  
Moene R.J., Ottenkamp J., Oppenheimer-Dekker A., Bartelings M.M., Transposition of the great arteries and narrowing of the aortic arch: Emphasis on right ventricular obstruction, Br Heart J, 53, pp. 58-63, (1985)
[10]  
Moller J.R., Edwards J.E., Interruption of aortic arch: Anatomic patterns and associated cardiac malformations, AJR, 95, pp. 557-563, (1965)