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Survival after systemic to pulmonary arterial shunts in infants less than 30 days old with obstructive lesions of the right heart chambers.

作者信息

Aziz K U, Olley P M, Rowe R D, Trusler G A, Mustard W T

出版信息

Am J Cardiol. 1975 Oct 6;36(4):476-83. doi: 10.1016/0002-9149(75)90897-8.

DOI:10.1016/0002-9149(75)90897-8
PMID:1190053
Abstract

Ninety-seven infants less than 30 days old with obstructive lesions of the right heart chambers underwent palliative surgery from 1950 through 1972. The diagnosis was made at cardiac catheterization and confirmed at operation or subsequent autopsy. Because of unavailability of complete preoperative studies and sufficient blood gas data, 36 patients presenting between 1950 and 1965 (Group I) were analyzed for surgical risk only. In 61 patients who underwent palliative procedures between 1966 and 1972 (Group II) a more detailed analysis was done. In this group, 31 had a Potts shunt, 29 a Waterston shunt and 1 a Blalock-Taussig shunt. The most frequently encountered malformation was severe tetralogy of Fallot (30 percent) with or without pulmonary atresia, followed by pulmonary atresia with intact ventricular septum (25 percent). The overall surgical mortality rate in patients seen after 1965 (Group II) was 34 percent compared with the 78 percent mortality rate in patients seen earlier (Group I). The surgical mortality in infants operated on during the 1st week of life was double that of those operated on in the 2nd through 4th weeks. Survivors were compared with nonsurvivors for timing of surgery, age at presentation and clinical profile. Only two significant differences were found. Preoperative continuous murmurs were more common in those who survived operation (13 of 40 patients) than in those who died (2 of 21). Arterial pH during cardiac catheterization was the best predictor of subsequent survival, nonsurvivors having significantly greater metabolic acidosis. Palliation of these severe lesions still carries a high mortality rate to which must be added the risk of subsequent repair. Our data suggest that primary repair is to be preferred if it can be undertaken with a risk approximating that of palliative procedures.

摘要

相似文献

1
Survival after systemic to pulmonary arterial shunts in infants less than 30 days old with obstructive lesions of the right heart chambers.
Am J Cardiol. 1975 Oct 6;36(4):476-83. doi: 10.1016/0002-9149(75)90897-8.
2
Systemic-pulmonary shunts in infants and children. Early and late results.婴幼儿的体肺分流。早期和晚期结果。
J Thorac Cardiovasc Surg. 1984 Jul;88(1):76-81.
3
Classic versus modified Blalock-Taussig shunts in neonates and infants.新生儿和婴儿的经典与改良布莱洛克-陶西格分流术
Circulation. 1985 Sep;72(3 Pt 2):II35-44.
4
The modified Blalock-Taussig shunt: clinical impact and morbidity in Fallot's tetralogy in the current era.改良布莱洛克-陶西格分流术:当代法洛四联症中的临床影响及发病率
J Thorac Cardiovasc Surg. 1997 Jul;114(1):25-30. doi: 10.1016/S0022-5223(97)70113-2.
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Modified Blalock-Taussig shunt in newborn infants.新生儿改良布莱洛克-陶西格分流术
J Thorac Cardiovasc Surg. 1984 Nov;88(5 Pt 1):770-5.
6
Classic shunting operations for congenital cyanotic heart defects.先天性青紫型心脏缺陷的经典分流手术。
J Thorac Cardiovasc Surg. 1982 Jul;84(1):88-96.
7
The Blalock-Taussig shunt. Low risk, effective palliation, and pulmonary artery growth.布莱洛克-陶西格分流术。低风险、有效的姑息治疗以及肺动脉生长。
J Thorac Cardiovasc Surg. 1983 Jun;85(6):917-22.
8
A comparison of Blalock-Taussig, Waterston, and polytetrafluoroethylene shunts in children less than two weeks of age.
Ann Thorac Surg. 1984 Jul;38(1):26-30. doi: 10.1016/s0003-4975(10)62180-7.
9
The Blalock-Taussig shunt in the first two years of life: a safe and effective procedure.出生后两年内的布莱洛克-陶西格分流术:一种安全有效的手术。
Ann Thorac Surg. 1978 Jul;26(1):38-41. doi: 10.1016/s0003-4975(10)63627-2.
10
Thirty-year follow-up of superior vena cava-pulmonary artery (Glenn) shunts.上腔静脉-肺动脉(格林)分流术30年随访
J Thorac Cardiovasc Surg. 1990 Nov;100(5):662-70; discussion 670-1.

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Pediatr Cardiol. 1983 Jul-Sep;4(3):183-8. doi: 10.1007/BF02242253.
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Use of saphenous vein allografts for aortopulmonary artery anastomoses in neonates with complex cyanotic congenital heart disease.
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