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法洛四联症和异常冠状动脉:使用人造管道已经过时。

Tetralogy of Fallot and abnormal coronary artery: use of a prosthetic conduit is outdated.

机构信息

Department of Pediatric Cardiac Surgery, Necker Sick Children Hospital-M3C, University Paris Descartes, Paris, France.

Department of Pediatric Cardiology, Necker Sick Children Hospital-M3C, University Paris Descartes, Paris, France.

出版信息

Eur J Cardiothorac Surg. 2019 Jul 1;56(1):94-100. doi: 10.1093/ejcts/ezz030.

Abstract

OBJECTIVES

Repair of tetralogy of Fallot (ToF) can be challenging in the presence of an abnormal coronary artery (CA) in 5-12% of cases. The aim of this study was to report our experience with ToF repair without the systematic use of a right ventricle-to-pulmonary artery (RV-PA) conduit.

METHODS

We conducted a monocentric retrospective study from 2000 to 2016, including 943 patients with ToF who underwent biventricular repair, of whom 8% (n = 76) presented with an abnormal CA. Mean follow-up time was 50 months (1 month-18 years).

RESULTS

The most frequent CA anomaly was the left descending artery arising from the right CA (n = 47, 61.8%). The median age at repair was 7.7 months (1.8 months-16 years). Thirteen patients (17%) required prior palliation, mostly systemic pulmonary shunts for anoxic spells in the neonatal period. Surgical repair allowed us to preserve the annulus in 40 patients (53%) by combining PA trunk plasty, commissurotomy and infundibulotomy under the abnormal CA. If the annulus had to be opened (n = 35, 46%), a transannular patch was inserted after a vertical incision of the PA trunk and extended obliquely on the RV over the anomalous crossing CA (with an infundibulotomy under the abnormal CA). Three patients (4%) required the insertion of an RV-PA conduit (1 valved tube and 2 RV-PA GORE-TEX tubes with annulus conservation). The early mortality rate was 4% (n = 3); none of the deaths was coronary related. Four patients (5%) required reoperation (2 early and 2 late reoperations) for residual pulmonary stenosis, 3 of whom had annulus preservation during the initial repair. The mean RV/left ventricle (LV) pressure ratio and an RV/LV pressure ratio >2/3 were identified as risk factors for right ventricular outflow tract (RVOT) reinterventions (P = 0.0026, P = 0.0085, respectively), RVOT reoperations (P = 0.0002 for both) and reoperation for RVOT residual stenosis (P = 0.0002, P = 0.0014, respectively). Two patients underwent pulmonary valve replacement. Freedom from late reoperation was 100% at 1 year, 97% at 5 years and 84% at 10 and 15 years.

CONCLUSIONS

Repair of ToF and abnormal CA can be performed without an RV-PA conduit, with an acceptable low reintervention rate. The high early mortality rate in this series remains a concern. If any doubt remains about the surgical relief of the RVOT obstruction, the RV/LV pressure ratio should always be measured in the operating room.

摘要

目的

在 5-12%的病例中,异常冠状动脉(CA)的存在会给法洛四联症(ToF)的修复带来挑战。本研究的目的是报告我们在不系统使用右心室至肺动脉(RV-PA)管道的情况下进行 ToF 修复的经验。

方法

我们进行了一项 2000 年至 2016 年的单中心回顾性研究,包括 943 例接受双心室修复的 ToF 患者,其中 8%(n=76)存在异常 CA。平均随访时间为 50 个月(1 个月至 18 年)。

结果

最常见的 CA 异常是左降支发自右 CA(n=47,61.8%)。修复时的中位年龄为 7.7 个月(1.8 个月至 16 岁)。13 名患者(17%)需要先前的姑息治疗,主要是新生儿期缺氧发作的体肺分流术。手术修复允许我们在 40 名患者(53%)中通过在异常 CA 下结合肺动脉干成形术、交界切开术和漏斗切开术来保留瓣环。如果必须打开瓣环(n=35,46%),则在肺动脉干垂直切开后插入跨瓣环补片,并在 RV 上斜向延伸越过异常交叉 CA(在异常 CA 下进行漏斗切开术)。3 名患者(4%)需要插入 RV-PA 管道(1 个带瓣管和 2 个 RV-PA GORE-TEX 管,带瓣环保留)。早期死亡率为 4%(n=3);无死亡与冠状动脉相关。4 名患者(5%)需要再次手术(2 例早期再次手术和 2 例晚期再次手术),以治疗残余的肺动脉瓣狭窄,其中 3 例在初次修复时保留了瓣环。RV/左心室(LV)压力比和 RV/LV 压力比>2/3 被确定为 RVOT 再干预(P=0.0026,P=0.0085)、RVOT 再次手术(两者均为 P=0.0002)和 RVOT 残余狭窄再次手术(P=0.0002,P=0.0014)的风险因素。2 名患者接受了肺动脉瓣置换术。1 年时无晚期再手术率为 100%,5 年时为 97%,10 年和 15 年时分别为 84%。

结论

在不使用 RV-PA 管道的情况下,可以对 ToF 和异常 CA 进行修复,且再干预率可接受。该系列中较高的早期死亡率仍令人担忧。如果对 RVOT 梗阻的手术缓解仍有任何疑问,应始终在手术室测量 RV/LV 压力比。

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