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Ann Thorac Surg 2001;71:1681-1682
© 2001 The Society of Thoracic Surgeons
a Division of Thoracic and Cardiovascular Surgery, Department of Surgery, University of Louisville, Louisville, Kentucky, USA
b Division of Cardiology, T. J. Sampson Hospital, Glasgow, Kentucky, USA
Accepted for publication June 4, 2000.
Address reprint request to Dr Bousamra, Division of Thoracic and Cardiovascular Surgery, Jewish Hospital and the University of Louisville, 201 Abraham Flexner Way, Suite 1200, Louisville, KY 40202
e-mail: bousamra{at}louisville.edu
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| Introduction |
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A 49-year-old diabetic man with post infarction angina and an occluded proximal left anterior descending (LAD) artery underwent a left IMA to LAD bypass through a lateral mini-thoracotomy approach. Symptomatic relief was achieved for 3 years until the development of chest pain on exertion. Coronary arteriography documented a widely patent IMA to LAD anastomosis and the presence of a large lateral branch arising from the IMA at the second intercostal space, that had quick washout of contrast into a proximal intercostal artery. Transcatheter coil embolization was performed and deemed successful, however, 6 months later, the patient had a recurrence of the chest pain. Myocardial ischemia was documented with the finding of a reversible defect in the anterior wall during exercise on a thallium perfusion scan. Repeat angiography showed the failed coiled obliteration of the branch (unwinding of the coil) (Fig 1) and a patent left IMA to LAD anastomosis. A video assisted thoracoscopic (VATS) approach was performed to control the anomalous IMA branch. With the patient in left lateral decubitus and using single lung ventilation, a wedge of 3 cm of the 8th rib at the midaxillary line was resected to allow easier instrumentation on the anterior chest wall and an additional trocar placed at the 5th space in the posterior axillary line for the placement of the 30° angle scope. The vessel was identified emerging from the 2nd intercostal space and meandering laterally under the pleura to feed several large intercostal collaterals. The culprit artery was clipped 3 cm after the lateral end of the coil, and before the first intercostal branch. The postoperative course was uneventful and the patient remains symptom-free 4 months after surgery.
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In contrast, sporadic case reports speak to its occurrence and is typically described as chest pain on exertion with angiographic identification of the IMA branch and resolution of symptoms after occlusion of the vessel [4]. Hartz and Heuser [8] recently described a case of IMA flow steal with ischemia documented on a thallium study that resolved after coil obliteration both clinically and by the normalization of the nuclear test. In our case, resolution of symptoms were seen transiently after the endovascular procedure until recanalization occurred, with recurrence of pain that later resolved after surgical control of the culprit collateral.
In this patient, the proximity of the medial end of the coil to the main IMA would have put at risk both the IMA and the flow to the LAD, and also the success of the collateral branch obliteration. The use of VATS allowed ligation of the vessel under vision with minimal morbidity and hospital stay.
This case illustrates that IMA flow steal can occur and shows the use of VATS as a valid surgical alternative to control IMA anomalous branches in the occasional patient with a failed endovascular procedure or whenever a repeat angiography represents high risk.
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