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用于法洛四联症合并肺动脉闭锁双侧肺动脉重建的蚌式切口。

The clamshell incision for bilateral pulmonary artery reconstruction in tetralogy of Fallot with pulmonary atresia.

作者信息

Luciani G B, Wells W J, Khong A, Starnes V A

机构信息

Division of Cardiothoracic Surgery, Children's Hospital Los Angeles, Calif, USA.

出版信息

J Thorac Cardiovasc Surg. 1997 Mar;113(3):443-52. doi: 10.1016/S0022-5223(97)70356-8.

Abstract

BACKGROUND

Patients with tetralogy of Fallot/pulmonary atresia often have bilateral pulmonary artery lesions, including diminutive central and peripheral vessels, major aortopulmonary collaterals, and distortion from previous operations. Staged procedures through lateral thoracotomies and median sternotomies have traditionally been used for repair.

METHODS

Between October 1993 and December 1995, 10 patients 3 months to 15 years old with complex tetralogy of Fallot/pulmonary atresia underwent repair via a clamshell approach. Nine had undergone a mean of 2.8 +/- 0.8 previous operations (range 1 to 4). Indications for operation were repair of pulmonary artery arborization anomalies in 10 (4 unilateral, 6 bilateral), with unifocalization in 6 (2 unilateral, 4 bilateral).

RESULTS

Eight of 10 patients had concomitant complete repair. There were no deaths at a mean follow-up of 17.1 +/- 4.0 months (range 12 to 26). Mean ventilation time was 3.7 +/- 2.1 days (range 1 to 14) and hospital stay 8.7 +/- 4.6 days (range 4 to 19). At follow-up, the peak right ventricular/left ventricular pressure ratio in patients who received complete repair was 0.44 +/- 0.13 (0.30 to 0.67). One patient (10%) required reoperation because of pseudoaneurysm of the main pulmonary artery 14 months after repair, and one had successful stent placement because of recurrent left and right pulmonary artery stenosis 8 months after repair. Two infants who underwent complete unifocalization and central pulmonary artery reconstruction are awaiting completion of repair.

CONCLUSIONS

The clamshell approach to complex tetralogy of Fallot/ pulmonary atresia provides simultaneous exposure of bilateral central and peripheral pulmonary artery lesions and intracardiac pathologic conditions. This procedure appears safe and may decrease the number of operations required to complete repair of tetralogy of Fallot/pulmonary atresia in selected patients.

摘要

背景

法洛四联症/肺动脉闭锁患者常伴有双侧肺动脉病变,包括中央和外周血管细小、主要体肺侧支血管以及既往手术造成的结构扭曲。传统上通过侧开胸和正中开胸分期手术进行修复。

方法

1993年10月至1995年12月,10例年龄3个月至15岁的复杂法洛四联症/肺动脉闭锁患者通过蛤壳式手术入路进行修复。9例患者既往平均接受过2.8±0.8次手术(范围1至4次)。手术指征为修复10例肺动脉分支异常(4例单侧,6例双侧),其中6例(2例单侧,4例双侧)进行了单灶化处理。

结果

10例患者中有8例同时进行了完全修复。平均随访17.1±4.0个月(范围12至26个月),无死亡病例。平均通气时间为3.7±2.1天(范围1至14天),住院时间为8.7±4.6天(范围4至19天)。随访时,接受完全修复患者的右心室/左心室压力峰值比为0.44±0.13(0.30至0.67)。1例患者(10%)在修复后14个月因主肺动脉假性动脉瘤需要再次手术,1例患者在修复后8个月因左右肺动脉反复狭窄成功置入支架。2例接受完全单灶化和中央肺动脉重建的婴儿正在等待完成修复。

结论

蛤壳式手术入路用于复杂法洛四联症/肺动脉闭锁可同时暴露双侧中央和外周肺动脉病变以及心内病理状况。该手术似乎安全,且可能减少部分患者完成法洛四联症/肺动脉闭锁修复所需的手术次数。

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