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改善右房异构的手术治疗结果。

Improving outcomes of the surgical management of right atrial isomerism.

机构信息

Department of Cardiovascular Surgery, Mt. Fuji Shizuoka Children's Hospital, Shizuoka, Japan.

出版信息

Ann Thorac Surg. 2012 Mar;93(3):832-8; discussion 838-9. doi: 10.1016/j.athoracsur.2011.05.110. Epub 2011 Nov 23.

Abstract

BACKGROUND

Patients with right atrial isomerism (RAI) have several cardiac malformations historically resulting in significant morbidity and mortality. We sought to assess whether current surgical strategies have improved the outcomes of patients with RAI.

METHODS

A retrospective review of our database from 1997 to 2010 identified 60 consecutive patients with RAI who underwent initial palliation at Mt. Fuji Shizuoka Children's Hospital. All of the patients had a functional single ventricle. Of the 60 patients, 33 patients (51.7%) had obstructed total anomalous pulmonary venous drainage (TAPVD), 23 patients (40.3%) had significant (more than moderate) atrioventricular valvular regurgitation (AVVR), 7 patients (12.3%) had hiatus hernia, and 4 patients (6.7%) had major aortopulmonary collateral arteries. Pulmonary outflow atresia was present in 39 of the patients (65%), and 46 patients had systemic-to-pulmonary artery shunts. Of the 33 patients with TAPVD, 18 underwent repair of the condition at initial palliation, 9 others at the time of a Glenn operation, 2 more through a Fontan operation, and 4 at the interstage between palliative surgeries. Eight of the 23 patients with significant AVVR underwent atrioventricular valve repair at initial palliation, 8 others at the time of Glenn operation, 4 others at the time of Fontan operation, and 3 during the interstage between operations. An initial neonatal surgical procedure was performed in 30 patients (50%). The mean follow-up period for patients in the study was 53.1 months.

RESULTS

Operative mortality after initial palliation was 15.4% (4 of 26 patients) before 2003 and 17.6% (6 of 34 patients) after 2004 (p=NS). Five-year survival was 53.8% before 2003 and 81.7% after 2004 (p=0.035, log-rank test). A multivariate analysis identified persistent AVVR of more than moderate degree (p=0.04) as a factor associated with late mortality.

CONCLUSIONS

The outcomes of surgery for RAI are improving. Neonatal palliative surgery for RAI carries a high operative risk of early mortality, and persistent significant AVVR remains a risk factor for late mortality.

摘要

背景

右房异构(RAI)患者既往存在多种心脏畸形,由此导致较高的发病率和死亡率。我们旨在评估当前的外科治疗策略是否改善了 RAI 患者的结局。

方法

我们对 1997 年至 2010 年富士山静冈儿童病院数据库进行回顾性分析,共纳入 60 例行初始姑息性治疗的 RAI 患者。所有患者均存在功能性单心室。60 例患者中,33 例(51.7%)存在完全性肺静脉异位引流(TAPVD)梗阻,23 例(40.3%)存在明显(中度以上)房室瓣反流(AVVR),7 例(12.3%)存在膈疝,4 例(6.7%)存在大型体肺侧支循环。39 例(65%)患者存在肺动脉瓣闭锁,46 例患者行体肺分流术。33 例 TAPVD 患者中,18 例在初始姑息性治疗时修复 TAPVD,9 例在 Glenn 手术时修复,2 例在 Fontan 手术时修复,4 例在姑息性手术间修复。23 例 AVVR 患者中,8 例在初始姑息性治疗时行房室瓣修复,8 例在 Glenn 手术时修复,4 例在 Fontan 手术时修复,3 例在手术间修复。30 例(50%)患者在新生儿期行初次手术。本研究患者的平均随访时间为 53.1 个月。

结果

2003 年前初次姑息性治疗后手术死亡率为 15.4%(26 例中的 4 例),2004 年后为 17.6%(34 例中的 6 例)(p=NS)。2003 年前 5 年生存率为 53.8%,2004 年后为 81.7%(p=0.035,log-rank 检验)。多变量分析显示,持续存在中重度 AVVR(p=0.04)是导致晚期死亡的因素。

结论

RAI 手术的结局正在改善。新生儿期行 RAI 姑息性手术的早期死亡率较高,持续存在的明显 AVVR 仍然是晚期死亡的危险因素。

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