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25例冠状静脉窦开窗患者的临床特征及手术结果

Clinical features and surgical outcome in 25 patients with fenestrations of the coronary sinus.

作者信息

Attenhofer Jost Christine H, Connolly Heidi M, Danielson Gordon K, Dearani Joseph A, Warnes Carole A, Jamil Tajik A

机构信息

Division of Cardiovascular Diseases, Mayo Clinic, Rochester, MN 55905, USA.

出版信息

Cardiol Young. 2007 Dec;17(6):592-600. doi: 10.1017/S1047951107001412. Epub 2007 Oct 24.

Abstract

OBJECTIVE

To analyze symptoms, associated anomalies, diagnostic approach, and surgical procedures in patients with partial fenestrations of the coronary sinus, a rare congenital disorder.

BACKGROUND

Partial fenestrations of the walls that usually separate the coronary sinus from the left atrium, also known as partial unroofing of the coronary sinus, may result in increased flow of blood to the lungs, cyanosis, or bidirectional shunting. The diagnosis is important, but difficult to confirm.

METHODS

We reviewed retrospectively the clinical, echocardiographic, operative, and follow-up data on 25 patients with partial fenestration of the coronary sinus. The patients had a median age of 8 years, and underwent cardiovascular surgery at Mayo Clinic between 1958 and 2003.

RESULTS

The initial diagnosis of a fenestration of the coronary sinus was made by the surgeon at repair of other congenital cardiac anomalies, by cardiac catheterization, or by echocardiography. In 14 patients, fenestration was missed during previous cardiovascular surgery. The most common associated cardiac lesions were atrial septal defects within the oval fossa, persistent left or right superior caval veins, and pulmonary or tricuspid atresia. In 7 patients, the symptoms were at least partially attributable to the fenestration, and included dyspnea, cerebral abscess, transient ischaemic attacks, and cyanosis. The fenestration was addressed surgically in 23 patients, and consisted of closure of the mouth of the coronary sinus, creation of an intra-atrial baffle, or direct repair of the fenestration. Death occurred in 1 patient due to complications unrelated to the repair. In the 24 early survivors, who have been followed up for a median of 85 months, 1 patient has died after a third reoperation for complex congenital cardiac disease.

CONCLUSIONS

Fenestrations of the coronary sinus are often missed in the preoperative evaluation of congenitally malformed hearts. When associated with right heart hypoplasia, atrial septal defect, or persistent superior caval vein, fenestrations of the coronary sinus should be considered as a possible additional finding. Once the diagnosis has been made, repair is straightforward.

摘要

目的

分析冠状静脉窦部分开窗这一罕见先天性疾病患者的症状、相关异常、诊断方法及手术操作。

背景

通常分隔冠状静脉窦与左心房的壁出现部分开窗,也称为冠状静脉窦部分未闭,可能导致肺血流量增加、发绀或双向分流。该诊断很重要,但难以确诊。

方法

我们回顾性分析了25例冠状静脉窦部分开窗患者的临床、超声心动图、手术及随访数据。这些患者的中位年龄为8岁,于1958年至2003年在梅奥诊所接受心血管手术。

结果

冠状静脉窦开窗的初步诊断是由外科医生在修复其他先天性心脏畸形时、通过心导管检查或超声心动图做出的。14例患者在之前的心血管手术中漏诊了开窗。最常见的相关心脏病变是卵圆窝内的房间隔缺损、持续左上腔静脉或右上腔静脉以及肺或三尖瓣闭锁。7例患者的症状至少部分归因于开窗,包括呼吸困难、脑脓肿、短暂性脑缺血发作和发绀。23例患者接受了手术治疗开窗,包括封闭冠状静脉窦口、创建心房内挡板或直接修复开窗。1例患者因与修复无关的并发症死亡。在24例早期存活者中,中位随访85个月,1例患者在因复杂先天性心脏病进行第三次再次手术后死亡。

结论

在先天性心脏畸形的术前评估中,冠状静脉窦开窗常被漏诊。当与右心发育不全、房间隔缺损或持续上腔静脉相关时,应考虑冠状静脉窦开窗这一可能的额外发现。一旦做出诊断,修复操作简单直接。

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