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法洛四联症的经心房-经肺动脉矫正术:一个发展中国家的经验

Transatrial-transpulmonary correction of tetralogy of Fallot: experience of a developing country.

作者信息

Souaga Kouassi Antonin, Bonny Rebecca, Katche Eric Koutoua, KiriouaKamenan Aime Yoboua, Amani Anderson Kwadjau, Degré Jean Calaire, Niava Randolph Gnamien, Kouamé Joseph, Yapo Paul, Kendja Flavien Kouassi

机构信息

Cardiovascular Surgery Department, the Abidjan Heart Institute, Abidjan, Ivory Coast.

Anesthesia and Intensive Care Department, the Abidjan Heart Institute, Abidjan, Ivory Coast.

出版信息

Kardiochir Torakochirurgia Pol. 2022 Sep;19(3):130-134. doi: 10.5114/kitp.2022.119760. Epub 2022 Oct 8.

DOI:10.5114/kitp.2022.119760
PMID:36268491
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9574585/
Abstract

INTRODUCTION

Right ventricular dysfunction is a cause of morbidity and mortality after surgical correction of tetralogy of Fallot. The transatrial-transpulmonary approach allows preservation of right ventricular function.

AIM

To report the immediate and long-term results of surgical treatment of tetralogy of Fallot using the transatrial-transpulmonary approach.

MATERIAL AND METHODS

This is a retrospective study including cases of tetralogy of Fallot operated on by the transatrial-transpulmonary approach between April 2009 and October 2010 in our institution.

RESULTS

There were 19 patients including 10 girls and 9 boys with a mean age of 7.4 years (extremes: 3 and 19 years). All our patients benefited from closure of the ventricular septal defect by a right atrial approach and enlargement of the pulmonary pathway. In the immediate postoperative period, the pressure gradient between the pulmonary artery and the right ventricle was 18.77 mm Hg. We had 2 deaths (10.5%). Complications were dominated by conduction disorders (100%) such as right bundle branch block and pleuropulmonary complications (41.20%). After a mean follow-up of 11.43 ±0.81 years, no patient died and all were asymptomatic, without significant residual lesion.

CONCLUSIONS

Complete cure of tetralogy of Fallot by the transatrial-transpulmonary route is associated with low morbidity and mortality in our experience. The long-term results are satisfactory.

摘要

引言

右心室功能障碍是法洛四联症手术矫正后发病和死亡的一个原因。经心房-肺动脉入路可保留右心室功能。

目的

报告采用经心房-肺动脉入路手术治疗法洛四联症的近期和远期结果。

材料与方法

这是一项回顾性研究,纳入了2009年4月至2010年10月在本机构采用经心房-肺动脉入路进行手术的法洛四联症病例。

结果

共有19例患者,其中10名女孩和9名男孩,平均年龄7.4岁(范围:3至19岁)。所有患者均通过右心房入路闭合室间隔缺损并扩大了肺动脉通道。术后即刻,肺动脉与右心室之间的压力梯度为18.77毫米汞柱。我们有2例死亡(10.5%)。并发症以传导障碍(100%)如右束支传导阻滞和胸膜肺部并发症(41.20%)为主。平均随访11.43±0.81年后,无患者死亡,所有患者均无症状,无明显残余病变。

结论

根据我们的经验,经心房-肺动脉途径完全治愈法洛四联症的发病率和死亡率较低。远期结果令人满意。

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本文引用的文献

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Outcome after surgical repair of tetralogy of Fallot: A systematic review and meta-analysis.法洛四联症手术修复后的结果:一项系统评价与荟萃分析。
J Thorac Cardiovasc Surg. 2020 Jan;159(1):220-236.e8. doi: 10.1016/j.jtcvs.2019.08.127. Epub 2019 Sep 25.
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Long-term outcomes of transatrial-transpulmonary repair of tetralogy of Fallot.法洛四联症经心房-肺动脉修复术的长期疗效
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Uncorrected tetralogy of fallot in a 25-year old nigerian african.一名25岁尼日利亚裔非洲人患未经矫正的法洛四联症。
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Transatrial-transpulmonary repair of tetralogy of Fallot.法洛四联症的经心房-经肺动脉修复术
Semin Thorac Cardiovasc Surg Pediatr Card Surg Annu. 2009:48-53. doi: 10.1053/j.pcsu.2009.01.005.
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Total transatrial correction of tetralogy of Fallot: no outflow patch technique.法洛四联症的经心房全矫治术:无流出道补片技术
Ann Thorac Surg. 2006 Oct;82(4):1316-21; discussion 1321. doi: 10.1016/j.athoracsur.2006.03.115.
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Follow-up after surgical closure of congenital ventricular septal defect.先天性室间隔缺损手术闭合后的随访
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Early results after transatrial/transpulmonary repair of tetralogy of Fallot.法洛四联症经心房/经肺动脉修复术后的早期结果。
Eur J Cardiothorac Surg. 2002 Oct;22(4):582-6. doi: 10.1016/s1010-7940(02)00403-7.
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Ann Thorac Surg. 2002 Jun;73(6):1794-800; discussion 1800. doi: 10.1016/s0003-4975(02)03586-5.
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How to diminish reoperation rates after initial repair of tetralogy of Fallot?法洛四联症初次修复术后如何降低再次手术率?
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