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单心室姑息术后不平衡型房室管缺损的双心室转换。

Biventricular conversion after single-ventricle palliation in unbalanced atrioventricular canal defects.

机构信息

Department of Cardiac Surgery, Children's Hospital Boston and Harvard Medical School, Boston, Massachusetts, USA.

出版信息

Ann Thorac Surg. 2013 Jun;95(6):2086-95; discussion 2095-6. doi: 10.1016/j.athoracsur.2013.01.075. Epub 2013 Apr 18.

Abstract

BACKGROUND

Management of unbalanced common atrioventricular canal (UCAVC) defect by a single-ventricle (SV) approach frequently results in poor outcomes, especially in trisomy 21 patients. In this report we describe our results with conversion to biventricular circulation in UCAVC patients with SV palliation.

METHODS

Retrospective review of patients with UCAVC undergoing biventricular conversion from prior SV palliation between 2003 and 2011 was conducted. Mortality and freedom from reinterventions were analyzed using nonparametric methods.

RESULTS

Sixteen children with UCAVC (8 patients [50%] were left dominant) and prior SV palliation underwent conversion to biventricular circulation between 2003 and 2011. Median follow-up was 18 months (range, 3 to 94 months). Surgical indications included worsening cyanosis, severe atrioventricular valve regurgitation, or failing bidirectional Glenn or Fontan physiology. All patients had either unequal distribution of the common atrioventricular valve of greater than 60% or one hypoplastic ventricle. By magnetic resonance imaging or computed tomography, 8 patients with right dominant atrioventricular canal had a median left ventricular end-diastolic volume of 32 mL/m(2) (range, 22 to 35 mL/m(2)). Eight patients with a left dominant atrioventricular canal had a median right ventricular end-diastolic volume of 42 mL/m(2) (range, 26 to 64 mL/m(2)). Eleven patients (69%) had trisomy 21, and 3 patients (19%) had heterotaxy. Stages of palliation included stage I in 2 patients, bidirectional Glenn in 10 patients, hemi-Fontan in 2 patients, and Fontan in 2 patients. There was 1 (6%) operative (right ventricle dominant) and 1 (6%) late death (left ventricle dominant). Eight patients required reinterventions, 3 (19%) surgical and 6 (38%) catheter-based. On follow-up, all had improvement in cyanosis and symptoms.

CONCLUSIONS

Biventricular conversion from failing SV palliation in UCAVC can be accomplished with an acceptable early and late morbidity and mortality, although need for reintervention was not uncommon.

摘要

背景

采用单心室(SV)方法治疗不均衡性共同房室管(UCAVC)缺陷,通常会导致不良结局,尤其是在 21 三体患者中。在本报告中,我们描述了对接受 SV 姑息治疗的 UCAVC 患者进行双心室转换的结果。

方法

对 2003 年至 2011 年间接受过双心室转换的 UCAVC 患者进行了回顾性研究。采用非参数方法分析死亡率和无再干预率。

结果

16 例 UCAVC 患者(8 例患者[50%]为左优势型)和先前接受过 SV 姑息治疗的患者在 2003 年至 2011 年间进行了双心室转换。中位随访时间为 18 个月(范围为 3 至 94 个月)。手术指征包括紫绀加重、严重房室瓣反流、双向 Glenn 或 Fontan 生理功能失败。所有患者均存在共同房室瓣分布不均,大于 60%或一个心室发育不良。通过磁共振成像或计算机断层扫描,8 例右优势型房室管患者的左心室舒张末期容积中位数为 32mL/m2(范围为 22 至 35mL/m2)。8 例左优势型房室管患者的右心室舒张末期容积中位数为 42mL/m2(范围为 26 至 64mL/m2)。11 例(69%)患者患有 21 三体综合征,3 例(19%)患者患有心脏异位。姑息性治疗分期包括 2 例Ⅰ期、10 例双向 Glenn、2 例半 Fontan 和 2 例 Fontan。手术死亡率为 1 例(6%)(右心室优势),晚期死亡率为 1 例(6%)(左心室优势)。8 例患者需要再次介入治疗,3 例(19%)为手术,6 例(38%)为导管介入。随访时,所有患者的紫绀和症状均有改善。

结论

从 UCAVC 失败的 SV 姑息治疗进行双心室转换可获得可接受的早期和晚期发病率和死亡率,尽管需要再次干预并不罕见。

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