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Anatomical Repair Conversion After Bidirectional Cavopulmonary Shunt for Complex Cardiac Anomalies: Palliation is Not a One-Way Path

机译:双向心脏分流后的解剖修复转化为复杂心肌异常:Palliation不是单向路径

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摘要

Abstract Complex cardiac anomalies are sometimes channeled toward Fontan palliation for various reasons. Nevertheless, anatomical repair after bidirectional cavopulmonary shunt may be another option with theoretical benefits. In this study, we report our experience with anatomical repair conversion in challenging patients who had been palliated with bidirectional cavopulmonary shunt. Retrospective review was conducted in patients who underwent anatomical repair conversion from prior bidirectional cavopulmonary shunt palliation between January 2008 and March 2016. Patients who underwent a planned staged 1?-ventricular repair were excluded. Twenty-three patients underwent anatomical repair conversion at a median age of 6.5?years (range 2.7–20.0?years). The interval time between palliation and conversion was 4.6?±?2.4?years (range 0.9–12.4). Indications for conversion were high-risk Fontan candidates ( n ?=?11) and preference for biventricular anatomy ( n ?=?12). In eight of the patients, bidirectional cavopulmonary shunts were taken down and superior vena cava was reconnected to the right atrium with Gore-Tex tube or bovine jugular venous tube. Mean cardiopulmonary bypass and aortic cross-clamp times were 225.6?±?107.0 and 138.3?±?76.6?min, respectively. After a mean follow-up of 2.7?±?2.2?years, there was no mortality and reoperation. No patients presented sinoatrial node dysfunction and superior venous cave stenosis. All the patients were in the New York Heart Association functional class I or II. Patients with previous bidirectional cavopulmonary shunt should be re-evaluated before completion of Fontan and, if cardiac anatomy allows, anatomical repair conversion may be considered, especially in patients with high-risk Fontan completion. Initial bidirectional cavopulmonary shunt palliation should not be considered as a one-way path to Fontan. Although technically challenging, early- and mid-term clinical results of anatomical repair conversion were satisfactory.
机译:摘要复杂心脏异常有时被引导到Fontan Palliation的原因。然而,双向肺胆总分流后的解剖修复可能是理论益处的另一种选择。在这项研究中,我们在挑战性患者中报告了我们在挑战性的患者中进行了解剖修复转化的经验。回顾性审查是在2008年1月至2016年1月至2016年3月至3月至3月至2016年3月的先前双向肺胆总分流姑息的患者进行解剖修复转化的患者中进行的审查。被排除在进行计划上演的患者1? - 诊断。二十三名患者在6.5年龄的中位数的中位数进行解剖修复转换,年龄(范围2.7-20.0?年)。间隔和转化之间的间隔时间为4.6?±2.4?年(范围0.9-12.4)。转化的适应症是高风险的Fontan候选者(N?=?11),并且偏好对五腹部解剖学(n?=?12)。在八个患者中,将双向肺胆总分流分流器抑制,并且通过血红蛋子或牛颈静脉管重新连接到右心房。平均心肺旁路和主动脉交叉钳位时间为225.6?±107.0和138.3?±76.6?min。平均随访2.7?±2.2?年,没有死亡率和重新进步。没有患者呈现鼻窦节点功能障碍和优异的静脉洞狭窄。所有患者都在纽约心脏关联功能级I或II中。患有先前双向肺胆管分流的患者应在完成Fontan之前重新评估,如果心脏解剖允许,可以考虑解剖修复转化,特别是在高风险的Fontan完成患者中。初始双向空穴分流间隙不应被视为Fontan的单向路径。虽然技术上挑战,初期和中期的解剖修复转化的临床结果令人满意。

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  • 来源
    《Pediatric cardiology》 |2018年第3期|共6页
  • 作者单位

    Pediatric Cardiac Surgery Center Fuwai Hospital National Center for Cardiovascular Disease;

    Pediatric Cardiac Surgery Center Fuwai Hospital National Center for Cardiovascular Disease;

    Pediatric Cardiac Surgery Center Fuwai Hospital National Center for Cardiovascular Disease;

    Pediatric Cardiac Surgery Center Fuwai Hospital National Center for Cardiovascular Disease;

    Pediatric Cardiac Surgery Center Fuwai Hospital National Center for Cardiovascular Disease;

    Pediatric Cardiac Surgery Center Fuwai Hospital National Center for Cardiovascular Disease;

    Pediatric Cardiac Surgery Center Fuwai Hospital National Center for Cardiovascular Disease;

    Pediatric Cardiac Surgery Center Fuwai Hospital National Center for Cardiovascular Disease;

    Pediatric Cardiac Surgery Center Fuwai Hospital National Center for Cardiovascular Disease;

  • 收录信息
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 儿科学;
  • 关键词

    Complex congenital heart defects; Glenn shunt; Single ventricle; Biventricular repair;

    机译:复杂的先天性心脏缺陷;格伦分流;单脑室;五年级修复;

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