Division of Pediatric Cardiology, Medical College of Wisconsin, Milwaukee, Wis.
Division of Cardiothoracic Surgery, Medical College of Wisconsin, Milwaukee, Wis.
J Thorac Cardiovasc Surg. 2018 Apr;155(4):1760-1768. doi: 10.1016/j.jtcvs.2017.11.003. Epub 2017 Nov 10.
Intramural anomalous aortic origin of a coronary artery (AAOCA) is associated with an increased risk of sudden cardiac death. This is amenable to surgical coronary unroofing, but outcomes studies are lacking.
To perform a comprehensive review of our institutional experience with pediatric patients with AAOCA who underwent surgical repair with unroofing of the intramural segment, focusing on preoperative and postoperative course and testing as well as intraoperative findings.
A retrospective cohort study was conducted to evaluate patients with AAOCA status post-coronary unroofing at Children's Hospital of Wisconsin. Data extraction included symptoms, preoperative and postoperative imaging and testing, surgical findings, and postoperative clinical course.
From January 1999 to December 12, 2015, 63 patients underwent unroofing at a median age of 13 years (0.5-18 years). The majority underwent unroofing of an intramural right coronary (79%); 21% had an intramural left AAOCA. Symptoms suggestive of possible ischemia were present in about 50%. Additional structural cardiac anomalies were present in 33%. Transthoracic echocardiography was diagnostic in 60 of 63 (95%) and correlated with surgical findings in all cases. There was no surgical mortality associated with the unroofing, and no additional coronary reinterventions were performed. The median duration of postoperative follow-up was 3.1 years (7 days to 13.6 years). Symptoms either persisted or developed in 46% postoperatively. Postoperative exercise stress testing, stress echocardiography, and cardiac magnetic resonance imaging were performed in 76%, 8%, and 20%, respectively, of the cohort. None identified findings consistent with reversible coronary ischemia. Three patients had sudden cardiac arrest (1 death) after surgery without an identified residual coronary abnormality.
Transthoracic echocardiography, with carefully designed coronary imaging protocols, can be diagnostic in accurately identifying intramural AAOCA in pediatric patients. Unroofing can be performed safely with no early morbidity, but symptoms can persist (including rare life-threatening events) without evidence of ischemia by postoperative provocative testing.
壁内异常起源的冠状动脉(AAOCA)与心脏性猝死风险增加有关。这种情况可以通过外科冠状动脉开窗术治疗,但缺乏相关的预后研究。
对我院接受冠状动脉开窗术治疗壁内 AAOCA 的儿科患者的手术修复经验进行全面回顾,重点关注术前和术后的病程及检查结果,以及术中发现。
对在威斯康星州儿童医院接受冠状动脉开窗术治疗的 AAOCA 患者进行回顾性队列研究。数据提取包括症状、术前和术后影像学和检查、手术发现和术后临床病程。
1999 年 1 月至 2015 年 12 月 12 日,63 例患者在中位年龄 13 岁(0.5-18 岁)时接受了冠状动脉开窗术。大多数患者接受了壁内右冠状动脉开窗术(79%);21%患者存在壁内左 AAOCA。约 50%的患者有提示可能存在缺血的症状。33%的患者存在其他结构性心脏畸形。63 例患者中有 60 例(95%)经胸超声心动图诊断,并与所有病例的手术发现相吻合。冠状动脉开窗术无手术相关死亡,也无进一步的冠状动脉介入治疗。术后中位随访时间为 3.1 年(7 天至 13.6 年)。46%的患者术后症状持续或出现。该队列中分别有 76%、8%和 20%的患者进行了术后运动应激试验、负荷超声心动图和心脏磁共振成像检查。这些检查均未发现可逆性冠状动脉缺血的表现。术后 3 例患者发生心脏骤停(1 例死亡),无明确残留冠状动脉异常。
经胸超声心动图,结合精心设计的冠状动脉成像方案,可准确诊断小儿患者的壁内 AAOCA。冠状动脉开窗术可安全进行,无早期并发症,但症状可持续存在(包括罕见的危及生命的事件),术后激发试验无缺血证据。