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婴儿期完全性肺静脉异位连接。十年经验,包括术后心室功能研究。

Total anomalous pulmonary venous connection in infancy. Ten years' experience including studies of postoperative ventricular function.

作者信息

Hammon J W, Bender H W, Graham T P, Boucek R J, Smith C W, Erath H G

出版信息

J Thorac Cardiovasc Surg. 1980 Oct;80(4):544-51.

PMID:7421289
Abstract

The surgical experience with total anomalous pulmonary venous connection (TAPVC) at the Venderbilt Hospital between the years 1969 and 1979 was reviewed. Twenty-five patients with TAPVC were studied. All but one patient presented at less than 1 year of age, and 11 patients were operated upon in the first 2 weeks of life. Operative mortality rate was 20% (5/25). Four of the five deaths were in critically ill neonates requiring preoperative ventilatory support. All operative deaths were in patients with pulmonary venous obstruction. All operative survivors have been followed for a mean 4.5 years (6 months to 10 years). There have been no late deaths or cases of symptomatic pulmonary venous obstruction. All children have had normal growth patterns. Ten patients have been recatheterized. Pulmonary artery systolic pressure, which was markedly elevated prior to operation, fell to normal levels after operation. Ventricular function has been evaluated by quantitative angiocardiography in nine patients before and after operation. Left ventricular size and function were markedly depressed preoperatively and rose to normal levels in postoperative survivors. Left atrial maximal volume was found to be 94% of normal values. These data support the contention that preoperative pulmonary venous obstruction is the single risk factor predicting higher risk of operative death. The presence of severe depression of left ventricular size and function preoperatively does not predict a higher operative risk, and postoperative survivors can expect normal ventricular function.

摘要

回顾了范德比尔特医院1969年至1979年间完全性肺静脉异位连接(TAPVC)的外科治疗经验。研究了25例TAPVC患者。除1例患者外,所有患者就诊时年龄均小于1岁,11例患者在出生后2周内接受了手术。手术死亡率为20%(5/25)。5例死亡患者中有4例是需要术前通气支持的危重新生儿。所有手术死亡患者均存在肺静脉梗阻。所有手术存活者均已接受平均4.5年(6个月至10年)的随访。无晚期死亡病例或有症状的肺静脉梗阻病例。所有儿童生长发育模式均正常。10例患者接受了再次心导管检查。术前明显升高的肺动脉收缩压术后降至正常水平。9例患者术前和术后通过定量心血管造影评估了心室功能。术前左心室大小和功能明显降低,术后存活者升至正常水平。左心房最大容积为正常值的94%。这些数据支持以下观点,即术前肺静脉梗阻是预测手术死亡高风险的单一危险因素。术前左心室大小和功能严重降低并不能预测更高的手术风险,术后存活者可预期心室功能正常。

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Total anomalous pulmonary venous connection in infancy. Ten years' experience including studies of postoperative ventricular function.婴儿期完全性肺静脉异位连接。十年经验,包括术后心室功能研究。
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引用本文的文献

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Unobstructive total anomalous pulmonary venous return: impact of early elective repair on the need for prolonged mechanical ventilatory support.无梗阻性完全性肺静脉异位引流:早期择期修复对延长机械通气支持需求的影响
Pediatr Cardiol. 2010 Nov;31(8):1191-7. doi: 10.1007/s00246-010-9788-4. Epub 2010 Sep 17.
2
[Surgical treatment of total anomalous pulmonary venous connection--clinical aspects of pulmonary venous obstruction].完全性肺静脉异位连接的外科治疗——肺静脉梗阻的临床情况
Jpn J Thorac Cardiovasc Surg. 1998 Nov;46(11):1126-32. doi: 10.1007/BF03217887.
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"Superimposition" digital subtraction angiography: evaluation of total anomalous pulmonary venous connection.
“叠加”数字减影血管造影:完全性肺静脉异位连接的评估
Pediatr Cardiol. 1993 Jan;14(1):47-8. doi: 10.1007/BF00794846.
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Total anomalous pulmonary venous connection. Repair using deep hypothermia and circulatory arrest in 44 consecutive infants.完全性肺静脉异位连接。44例连续婴儿采用深低温停循环进行修复。
Br Heart J. 1982 Sep;48(3):249-54. doi: 10.1136/hrt.48.3.249.
5
The value of early repair for total anomalous pulmonary venous drainage.
Pediatr Cardiol. 1985;6(2):77-81. doi: 10.1007/BF02282742.