经导管冠状动脉瘘闭合:单中心经验

H. Mahla, Jayaranganath Mahimarangaiah, Usha Mandikal Kodanda Rama Sastry, S. Chikkaswamy, P. Bhat, C. Manjunath
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引用次数: 1

摘要

背景:经导管冠状动脉瘘闭合已成为手术的替代方法。冠状动脉瘘的治疗是复杂的,建议是基于轶事病例或非常小的回顾性系列。目的:本研究的目的是确定经导管冠状动脉瘘闭合术的安全性、可行性以及即时和中期随访结果。方法:回顾2011年1月至2014年5月期间所有出现显著冠状动脉瘘的患者的记录。那些有其他复杂心脏疾病需要手术治疗的患者被排除在研究之外。在2011年1月至2014年3月期间,共有9例11个月至58岁的先天性冠状动脉瘘患者采用各种装置经皮经导管闭合。立即关闭结果和临床随访使用数据库或电话到中心的信息进行审查。结果:右冠状动脉瘘4例(44.4%),左旋冠状动脉瘘3例(33.3%),左前降支瘘2例(22.2%)。引流部位为右心房5例(55.6%),右心室2例(22.2%),左心室1例(11.1%),冠状窦1例(11.1%)。所有患者(100%)使用各种装置成功完成了经导管闭合。器械部署后的血管造影显示7例患者(77.7%)完全闭塞,2例患者(22.2%)轻微至轻度残留血流。2例患者(22.2%)术后出现短暂性ST-T波改变。4例(44.4%)患者使用Amplatzer血管塞II, 3例(33.3%)患者使用Amplatzer导管闭塞器II, 2例(22.2%)患者使用Lifetech导管闭塞器。术后1个月左室舒张末期容积从平均基线值82.77±4.55 ml/ m2降至77.22±3.49 ml/ m2 (P = 0.001),术后2个月所有患者均恢复正常。在随访1个月时,心胸比从平均基线值0.57±0.035降至0.53±0.02,随访2个月时进一步降至0.50±0.007 (P < 0.001)。随访100%完成,随访时间为2个月至3年(平均= 1.44±0.79年)。没有早死或晚死。所有患者在关闭后1个月无症状,除了1例患者(11%)在随访3个月前有轻微的残余分流,并在药物治疗下用力呼吸困难。1例患者(11%)伴有第二口房间隔缺损,经皮缝合。结论:经导管封堵冠状动脉瘘是可行且安全的,对大多数患者来说是一种有希望的替代手术的方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Transcatheter closure of coronary arterial fistula: A single-center experience
Background: Transcatheter closure of coronary artery fistula has emerged as an alternative to surgery. The management of coronary artery fistula is complicated, and recommendations have been based on anecdotal cases or very small retrospective series. Objective: The objective of this study is to determine the safety, feasibility, and immediate and intermediate follow-up results of the transcatheter closure of coronary arterial fistula. Methods: We reviewed the records of all patients presenting with significant coronary arterial fistulae between January 2011 and May 2014. Those with additional complex cardiac disease requiring surgical management were excluded from the study. A total of nine patients aged 11 months to 58 years with congenital coronary arterial fistulae underwent percutaneous transcatheter closure using various devices between January 2011 and March 2014. The immediate closure results and clinical follow-up were reviewed using information from a database or telephone calls to the center. Results: Fistulae originated from the right coronary artery in 4 patients (44.4%), left circumflex coronary artery in 3 patients (33.3%), and left anterior descending coronary artery in 2 patients (22.2%). The drainage site was the right atrium in 5 patients (55.6%), right ventricle in 2 patients (22.2%), left ventricle in 1 patient (11.1%), and coronary sinus in 1 patient (11.1%). All of the patients (100%) underwent successful transcatheter closure using the various devices. Angiography after device deployment revealed complete occlusion in 7 patients (77.7%) and trivial to mild residual flow in 2 patients (22.2%). Two patients (22.2%) had transient ST-T wave changes after the procedure. The Amplatzer Vascular Plug II was used in four patients (44.4%), Amplatzer Duct Occluder II was used in three patients (33.3%), and Lifetech Duct Occluder was used in two patients (22.2%). The left ventricular end-diastolic volume decreased from a mean baseline value of 82.77 ± 4.55 ml/m 2 to 77.22 ± 3.49 ml/m 2 at 1 month after the procedure (P = 0.001) and had normalized in all of the patients at 2 months postprocedure. The cardiothoracic ratio decreased from a mean baseline value of 0.57 ± 0.035 to 0.53 ± 0.02 at the 1-month follow-up and further decreased to 0.50 ± 0.007 at 2 months (P < 0.001). Follow-up was 100% complete and ranged from 2 months to 3 years (mean = 1.44 ± 0.79 years). There were no early or late deaths. All of the patients were asymptomatic at 1 month postclosure, except one patient (11%) who had a mild residual shunt until 3 months of follow-up and dyspnea on exertion that was medically managed. One patient (11%) had an associated ostium secundum atrial septal defect that was percutaneously closed. Conclusion: Transcatheter closure of coronary arterial fistula is feasible and safe in anatomically suitable vessels and is a promising alternative to surgery in most patients.
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