Liu P R, Leong K H, Lee P C, Chen Y T
Department of Surgery, Taichung Veterans General Hospital, Taiwan, R.O.C.
Zhonghua Yi Xue Za Zhi (Taipei). 1994 Sep;54(3):160-5.
Congenital coronary artery fistula is a rare heart defect. Symptoms of the patient and characteristics of the fistula were investigated and the role of surgical treatment was evaluated.
Fourteen patients with congenital coronary artery fistulae were diagnosed here between January, 1983, and December, 1991. Only one patient was asymptomatic, but diagnosis was suspected from clinical presentation of a continuous murmur. In the 13 symptomatic patients, angina and exertional dyspnea were the most common symptoms. Congestive heart failure and subacute bacterial endocarditis were rare complications. Cardiac catheterization with selective coronary angiography was performed in all of these patients. The left anterior descending coronary artery was most commonly involved in this series. Findings, different from those in other literature, were the right coronary artery has more usually been reported. Fistulous communication was most often found in the pulmonary artery, right ventricle and right atrium. The mean ratio of pulmonary-to-systemic flow was 1.67 in 10 patients, and the shunt flow of another 4 accidentally diagnosed patients was trivial. Six patients, including all 4 patients, age < 20 years at diagnosis, underwent surgical correction; only 1 patient was not given an aid of cardiopulmonary bypass.
The six patients who received surgical treatment, one died of pneumonia and respiratory failure and the other five patients had no evidence of residual fistula. All five were asymptomatic during a mean follow-up period of five years. The symptoms were slowly progressive, and functional status worsened in two who refused operation and in two high risk patients. In four patients with accidentally diagnosed small fistulae, the symptoms remained unchanged during six years of follow-up.
The objective of surgical treatment was closure of the fistula tract without compromise of normal flow through the coronary artery. Surgical intervention was recommended for all symptomatic patients and asymptomatic young patients as well, to prevent the development of fistula-related complications.
先天性冠状动脉瘘是一种罕见的心脏缺陷。对患者的症状及瘘管特征进行了研究,并评估了手术治疗的作用。
1983年1月至1991年12月期间,在此诊断出14例先天性冠状动脉瘘患者。仅1例患者无症状,但根据连续性杂音的临床表现怀疑有诊断。在13例有症状的患者中,心绞痛和劳力性呼吸困难是最常见的症状。充血性心力衰竭和亚急性细菌性心内膜炎是罕见的并发症。所有这些患者均进行了选择性冠状动脉造影的心脏导管检查。在本系列中,左前降支冠状动脉最常受累。与其他文献不同的是,本研究发现右冠状动脉受累更为常见。瘘管最常出现在肺动脉、右心室和右心房。10例患者的肺循环与体循环血流量平均比值为1.67,另外4例意外诊断患者的分流流量很小。6例患者,包括所有4例诊断时年龄<20岁的患者,接受了手术矫正;仅1例患者未使用体外循环辅助。
接受手术治疗的6例患者中,1例死于肺炎和呼吸衰竭,另外5例患者无残余瘘管迹象。在平均5年的随访期内,所有5例患者均无症状。症状呈缓慢进展,2例拒绝手术的患者和2例高危患者的功能状态恶化。4例意外诊断为小瘘管的患者,在6年的随访期间症状未变。
手术治疗的目的是闭合瘘管,同时不影响冠状动脉的正常血流。建议对所有有症状的患者以及无症状的年轻患者进行手术干预,以预防与瘘管相关并发症的发生。