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[部分性肺静脉异位引流的外科治疗]

[Surgical treatment of partial anomalous pulmonary venous drainage].

作者信息

Cabrera A, Idígoras G, Sarrionandía M J, Martínez P, Rumoroso J R, Alcíbar J

机构信息

Servicios de Cardiología Pediátrica, Hospital Infantil de Cruces, Baracaldo, Vizcaya.

出版信息

Rev Esp Cardiol. 1996 Feb;49(2):130-5.

PMID:8948723
Abstract

OBJECTIVES

We studied all patients operated for partial anomalous pulmonary venous drainage and half-time follow-up.

MATERIALS AND METHODS

Twenty-eight patients with a mean age of 5 +/- 5 years (5 patients were less than 1 year old). There were sixteen male and twelve female patients. Thirteen patients were symptomatic (47%). The drainage was to the superior vena cava in thirteen cases, to the inferior vena cava in eight cases, to the right atrium in five cases, mixed (to the superior vena cava and to the inferior vena cava) in one case and to the innominate vein in one patient. The diagnosis was made through echocardiography and catheterization in 25 patients, whereas nuclear magnetic resonance was performed in the last five patients. All cases were corrected through medium thoracotomy, except for the single case in which the drainage was to the innominate vein). In 27 patients, the pulmonary veins were guided to the left atrium through an enlarged present atrial septal defect or through a created atrial septal defect. In one case a direct connection was performed from the veins to the left atrium. After the surgical correction, all patients underwent a color-coded Doppler echocardiography study and a nuclear magnetic resonance study was performed in five patients.

RESULTS

Twenty-seven patients survived after surgical correction. The patient with a mixed drainage developed an obstruction of the superior vena cava, the pressure gradient was 9 mmHg. He required a second surgical procedure followed with angioplasty on two occasions during a six month period. Two patients showed an ectopic atrial rhythm at some late time. The patient who died was one month old and had an associated pulmonary parenchymal sequestration.

CONCLUSION

Partial anomalous venous connection is a congenital heart disease which has an easy surgical correction. Complications may arise after the surgical correction, among them obstruction of the superior vena cava and arrythmias are most frequently found. Obstruction is present when 50% of the caval area is occupied by the patch. The arrythmias occur following all surgical techniques. In order to decrease the arrythmias it is necessary to perform a good hemosthasis at the site of the patch, to leave the sinus node free of compression and to perform the atrial incision at the posterior wall. The diagnosis and the follow-up can be performed with non-invasive procedures.

摘要

目的

我们对所有接受部分性肺静脉异位引流手术的患者进行了研究并进行了中期随访。

材料与方法

28例患者,平均年龄5±5岁(5例患者年龄小于1岁)。男性16例,女性12例。13例患者有症状(47%)。肺静脉引流至上腔静脉13例,至下腔静脉8例,至右心房5例,混合性(至上腔静脉和下腔静脉)1例,至无名静脉1例。25例患者通过超声心动图和心导管检查确诊,最后5例患者进行了核磁共振检查。除1例引流至无名静脉的患者外,所有病例均通过正中开胸手术进行矫正。27例患者中,肺静脉通过扩大的卵圆孔未闭或人工制造的房间隔缺损引导至左心房。1例患者进行了静脉与左心房的直接连接。手术矫正后,所有患者均接受了彩色编码多普勒超声心动图检查,5例患者进行了核磁共振检查。

结果

27例患者手术矫正后存活。混合性引流的患者发生了上腔静脉梗阻,压力阶差为9 mmHg。他在6个月内需要进行第二次手术,并两次进行血管成形术。2例患者在后期出现异位心律。死亡患者为1个月大,合并肺实质隔离症。

结论

部分性肺静脉异位连接是一种先天性心脏病,手术矫正容易。手术矫正后可能出现并发症,其中最常见的是上腔静脉梗阻和心律失常。当上腔静脉区域50%被补片占据时会出现梗阻。所有手术技术后都会发生心律失常。为了减少心律失常,有必要在补片部位进行良好的止血,使窦房结不受压迫,并在心房后壁进行心房切口。诊断和随访可以通过非侵入性检查进行。

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