Department of Cardiothoracic Surgery, Shanghai Children's Medical Center, Shanghai Jiaotong University School of Medicine, Shanghai, China.
Department of Cardiothoracic Surgery, Shanghai Children's Medical Center, Shanghai Jiaotong University School of Medicine, Shanghai, China.
J Thorac Cardiovasc Surg. 2016 Oct;152(4):1123-1130.e1. doi: 10.1016/j.jtcvs.2016.04.093. Epub 2016 May 10.
Isolated congenital coronary artery fistula is a rare condition, and the surgical experience for treating this condition is limited.
This was a retrospective review of 47 patients who underwent surgical repair of isolated congenital coronary artery fistula from January 2001 to March 2015.
All but 1 patient presented with no symptoms. The median age at operation was 3.9 years (range, 0.4-15.2 years), and the median weight was 15.2 kg (range, 6.3-77.0 kg). Right coronary artery to right ventricle fistula was the most common pattern, which was present in 16 patients. Epicardial ligation without cardiopulmonary bypass was used to treat 4 patients, whereas cardiopulmonary bypass was used in the remaining 43 patients. Surgical techniques included transcoronary closure in 20 patients, transcameral or transpulmonary closure in 20 patients, a combination of both transcameral and transcoronary closure in 2 patients, and a conversion from transcameral closure to epicardial ligation in 1 patient. There were no deaths during our study period. Injury to the mitral valve occurred in 1 patient. Residual shunt was observed in 8 patients, 2 of which closed spontaneously during the follow-up. Extracardiac repair was associated with a higher risk of recanalization (P = .004). Freedom from recanalization was 89.4%, 85.1%, 83.0%, and 83.0% at discharge, 6 months, 1 year, and 5 years postsurgery, respectively. Two patients required transcatheter closure for residual shunts.
Surgical repair of isolated congenital coronary artery fistula in pediatric patients can be performed with low mortality and morbidity. Careful evaluation after surgery is necessary to monitor the occurrence of residual shunt.
孤立性先天性冠状动脉瘘是一种罕见的疾病,其治疗经验有限。
这是一项回顾性研究,共纳入了 2001 年 1 月至 2015 年 3 月期间接受手术治疗的 47 例孤立性先天性冠状动脉瘘患者。
除 1 例患者外,所有患者均无明显症状。手术时的中位年龄为 3.9 岁(范围:0.415.2 岁),中位体重为 15.2kg(范围:6.377.0kg)。右冠状动脉至右心室瘘是最常见的类型,共 16 例。4 例患者采用心外膜结扎术,不使用体外循环,其余 43 例患者采用体外循环。手术技术包括 20 例经冠状动脉封堵术、20 例经心腔或经肺封堵术、2 例同时采用经心腔和经冠状动脉封堵术、1 例由经心腔封堵术改为心外膜结扎术。研究期间无死亡病例。1 例患者二尖瓣受损。8 例患者存在残余分流,其中 2 例在随访期间自行闭合。心外修补与再通风险增加相关(P=0.004)。术后出院时、术后 6 个月、1 年和 5 年的无再通率分别为 89.4%、85.1%、83.0%和 83.0%。2 例患者残余分流需行经导管封堵。
小儿孤立性先天性冠状动脉瘘的手术治疗可获得较低的死亡率和发病率。术后需仔细评估以监测残余分流的发生。