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Characteristics of Congenital Coronary Artery Fistulas Complicated with Infective Endocarditis: Analysis of 25 Reported Cases

机译:先天性冠状动脉瘘并发感染性心内膜炎的特征:报道的25例病例的分析

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Congenital coronary artery fistulas (CAFs) are infrequent congenital coronary artery anomalies. Complications such as left-to-right shunt, congestive heart failure, myocardial infarction, pericardial effusion, aneurysm formation, rupture, hemopericardium, pulmonary hypertension, infective endocarditis (IE), syncope, stroke, and sudden death may occur with a variable low frequency. To describe the clinical characteristics of patients with CAFs complicated by IE. A search was conducted through PubMed using the terms "CAFs" and "IE." Papers with a full description of the fistula characteristics and detailed data regarding bacterial endocarditis were included for evaluation. In the overall group of reviewed subjects (n = 25, 9 females), the mean patient age was 42.5 years (range: 16 and 87). The right coronary artery (RCA) and left coronary artery (LCA) contributed equally to fistula formation. Terminations into the right heart side occurred in 19 (76%) fistulas. The majority of the fistulas (92%) were unilateral. The cultured microorganism was Streptococcus in 14 (56%) and Staphylococcus in 4 (16%) of the reviewed subjects. Echocardiographic single or multiple valvular regurgitation was found in 8 (32%) of the reviewed subjects. Small and large intracardiac vegetations were detected in 18 patients (72%). Antibiotic therapy was initiated in 20 (80%) subjects and 16 fistulas were treated surgically. During surgery, spontaneous closure of the fistula was observed in one patient. Percutaneous therapeutic embolization (PTE) was successfully performed in two subjects. CAFs complicated by IE may affect all age groups with a slight male preponderance. Unilateral fistulas, either arising from the right or left coronary artery, are predominant, draining mainly into the right heart side. It is emphasized that antibiotic prophylaxis is strongly advised for pediatric and adult patients with congenital CAFs.
机译:先天性冠状动脉瘘(CAF)是罕见的先天性冠状动脉异常。从左向右分流,充血性心力衰竭,心肌梗塞,心包积液,动脉瘤形成,破裂,出血性心包积血,肺动脉高压,感染性心内膜炎(IE),晕厥,中风和猝死等并发症可能会以可变的低频发生。描述并发IE的CAF患者的临床特征。通过PubMed使用“ CAFs”和“ IE”这两个词进行了搜索。评价中包括完整描述瘘管特征的论文和有关细菌性心内膜炎的详细数据。在全部受检对象中(n = 25,9位女性),平均患者年龄为42.5岁(范围:16和87)。右冠状动脉(RCA)和左冠状动脉(LCA)对瘘管形成的贡献相同。终止于右心脏一侧的有19例(76%)瘘管。多数瘘管(92%)是单侧的。培养的微生物是14例(56%)的链球菌和4例(16%)的葡萄球菌。超声心动图单瓣或多瓣膜反流被发现在8(32%)的审查对象。在18例患者中检出了大小不一的心内植被(72%)。在20名(80%)受试者中开始了抗生素治疗,并对16例瘘进行了手术治疗。在手术过程中,观察到一名患者的瘘管自发闭合。在两个受试者中成功进行了经皮治疗栓塞(PTE)。伴有IE的CAF可能会影响所有年龄段,男性占优势。右侧或左侧冠状动脉产生的单侧瘘管占主导地位,主要排入右侧心脏侧。需要强调的是,强烈建议对先天性CAF的儿科和成年患者进行抗生素预防。

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