Bigler Marius Reto, Huber Adrian Thomas, Räber Lorenz, Gräni Christoph
Department of Cardiology, Inselspital, Bern University Hospital, University of Bern, Freiburgstrasse 18, CH-3010 Bern, Switzerland.
Department of Diagnostic, Interventional and Paediatric Radiology, Inselspital, Bern University Hospital, University of Bern, Bern, Switzerland.
Eur Heart J Case Rep. 2021 Mar 4;5(3):ytab081. doi: 10.1093/ehjcr/ytab081. eCollection 2021 Mar.
Anomalous aortic origin of a coronary artery (AAOCA) is a rare congenital disease associated with an increased risk of myocardial ischaemia, ventricular arrhythmias, and heart failure.
A 75-year-old Caucasian man was referred for invasive coronary angiography (ICA) due to atypical chest pain. Invasive coronary angiography demonstrated non-significant atherosclerotic disease of the left coronary artery and an anomalous origin of the right coronary artery (RCA); without selective intubation. Coronary computed tomography angiography (CCTA) revealed a right-AAOCA with interarterial and intramural course, and a soft plaque in the distal RCA. Subsequent physical-stress single-photon emissions computed tomography (SPECT) showed exercise-induced inferoapical myocardial ischaemia, giving a Class IC level of evidence for surgical correction of the AAOCA. Repeated ICA with selective R-AAOCA intubation confirmed an 80% distal atherosclerotic stenosis, which was treated with direct stenting. Subsequent invasive physiologic evaluation under maximal dobutamine-volume challenge (gradually increasing dose of dobutamine max. 40 μg/kg per body weight/min, 3000 mL ringer lactate and 1 mg atropine was given until the patient reached a maximum of 145 b.p.m.), revealed a haemodynamically non-relevant anomalous segment with a fractional flow reserve (FFR) of 0.91. A follow-up SPECT was normal, and the patient was completely symptom-free at 1 month.
We present the sequential diagnostic approach in a symptomatic patient with a right anomalous coronary artery and concomitant atherosclerotic disease. Using this approach, the patient could be deferred from guideline recommended open-heart surgery of the AAOCA, as direct invasive dobutamine/volume FFR revealed haemodynamic non-relevance of the anomalous segment after stenting the concomitant atherosclerotic stenosis in the distal segment within the same coronary artery.
冠状动脉异常起源(AAOCA)是一种罕见的先天性疾病,与心肌缺血、室性心律失常和心力衰竭风险增加相关。
一名75岁的白种男性因非典型胸痛被转诊进行有创冠状动脉造影(ICA)。有创冠状动脉造影显示左冠状动脉存在非显著性动脉粥样硬化疾病,右冠状动脉(RCA)起源异常;未进行选择性插管。冠状动脉计算机断层扫描血管造影(CCTA)显示为右AAOCA,走行于动脉间和壁内,并在RCA远端有一个软斑块。随后的运动负荷单光子发射计算机断层扫描(SPECT)显示运动诱发下壁心尖部心肌缺血,为AAOCA手术矫正提供了IC类证据水平。重复进行ICA并对R-AAOCA进行选择性插管,证实存在80%的远端动脉粥样硬化狭窄,采用直接支架置入术进行治疗。随后在最大多巴酚丁胺-容量负荷挑战下(多巴酚丁胺剂量逐渐增加,最大为40μg/kg体重/分钟,给予3000mL乳酸林格液和1mg阿托品,直至患者心率达到最大145次/分钟)进行有创生理评估,结果显示该异常节段血流动力学无显著意义,血流储备分数(FFR)为0.91。随访SPECT正常,患者在1个月时完全无症状。
我们展示了一名有症状的右冠状动脉异常并伴有动脉粥样硬化疾病患者的序贯诊断方法。采用这种方法,该患者可不必接受指南推荐的AAOCA心脏直视手术,因为在同一冠状动脉远端节段对伴发的动脉粥样硬化狭窄进行支架置入后,直接有创多巴酚丁胺/容量FFR显示该异常节段血流动力学无显著意义。