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先天性青紫型心脏缺陷的经典分流手术。

Classic shunting operations for congenital cyanotic heart defects.

作者信息

Arciniegas E, Farooki Z Q, Hakimi M, Perry B L, Green E W

出版信息

J Thorac Cardiovasc Surg. 1982 Jul;84(1):88-96.

PMID:7087545
Abstract

A total of 297 consecutive classic systemic artery-pulmonary artery shunts were performed in 281 patients over the past 9 years. This experience includes 200 Blalock-Taussig shunts (67.3%), 84 Waterston shunts (28.2%), and 13 Potts shunts (4.3%). The overall early mortality after the Blalock-Taussig shunt (5.5%) was significantly lower (p less than 0.02) than for the Waterston shunt (13%). The early mortality after either the Blalock-Taussig or Waterston shunt was not statistically related to the age of the patient at operation. Both the Blalock-Taussig and Waterston shunts demonstrated a higher mortality (p less than 0.02) among patients in Group II (complex defects) than in patients in Group I (tetralogy of Fallot and pulmonary atresia with ventricular septal defect [VSD]). However, the Blalock-Taussig shunt had a significantly lower (p less than 0.04) probability of early postoperative death than the Waterston shunt among patients with complex lesions. The Blalock-Taussig shunt also revealed a lower incidence of important late postoperative complications and did not affect adversely the hemodynamic result after intracardiac correction, as evidenced by late postoperative cardiac catheterization. This study also confirms the feasibility of the Blalock-Taussig shunt during the neonatal period without significantly increased age-related risk of postoperative death (p = 0.13) and with good early and late long-term patency rates.

摘要

在过去9年中,共对281例患者进行了297例连续性经典体动脉-肺动脉分流术。该经验包括200例Blalock-Taussig分流术(67.3%)、84例Waterston分流术(28.2%)和13例Potts分流术(4.3%)。Blalock-Taussig分流术后的总体早期死亡率(5.5%)显著低于Waterston分流术(13%)(p<0.02)。Blalock-Taussig或Waterston分流术后的早期死亡率与手术时患者的年龄无统计学相关性。Blalock-Taussig分流术和Waterston分流术在II组(复杂缺损)患者中的死亡率均高于I组(法洛四联症和室间隔缺损[VSD]合并肺动脉闭锁)患者(p<0.02)。然而,在患有复杂病变的患者中,Blalock-Taussig分流术术后早期死亡的概率显著低于Waterston分流术(p<0.04)。Blalock-Taussig分流术还显示术后晚期重要并发症的发生率较低,且如术后晚期心导管检查所示,对心内矫正后的血流动力学结果无不良影响。本研究还证实了Blalock-Taussig分流术在新生儿期的可行性,术后死亡的年龄相关风险没有显著增加(p = 0.13),且早期和晚期长期通畅率良好。

相似文献

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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。
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引用本文的文献

1
Obstruction of the central pulmonary artery after shunt operations in patients with pulmonary atresia.肺动脉闭锁患者分流手术后中央肺动脉梗阻
Br Heart J. 1987 Jun;57(6):534-42. doi: 10.1136/hrt.57.6.534.
2
Balloon dilatation of the pulmonary valve in the first year of life in patients with tetralogy of Fallot: a preliminary study.法洛四联症患者1岁以内肺动脉瓣球囊扩张术:一项初步研究。
Br Heart J. 1988 Sep;60(3):232-5. doi: 10.1136/hrt.60.3.232.
3
Balloon dilatation of stenosed Blalock-Taussig shunts.狭窄的布莱洛克-陶西格分流术的球囊扩张术。
Br Heart J. 1989 May;61(5):432-4. doi: 10.1136/hrt.61.5.432.
4
Growth of the pulmonary artery after neonatal balloon dilatation of the right ventricular outflow tract in an infant with the tetralogy of Fallot and atrioventricular septal defect.法洛四联症合并房室间隔缺损婴儿右心室流出道新生儿球囊扩张术后肺动脉的生长情况。
Br Heart J. 1989 Jul;62(1):65-8. doi: 10.1136/hrt.62.1.65.
5
Modified versus classical Blalock-Taussig shunts for congenital cyanotic heart diseases: a comparison of long-term results.
Jpn J Surg. 1987 Nov;17(6):470-7. doi: 10.1007/BF02470751.