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Abul Hasan Muhammad Bashar
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Ann Thorac Surg 2006;81:2079-2083
© 2006 The Society of Thoracic Surgeons


Original article: Cardiovascular

Total Aortic Arch Replacement in Patients With Arch Vessel Anomalies

Kazuchika Suzuki, MD, PhD * , Teruhisa Kazui, MD, PhD, Abul Hasan Muhammad Bashar, MBBS, PhD, Katsushi Yamashita, MD, PhD, Hitoshi Terada, MD, PhD, Naoki Washiyama, MD, PhD, Takayasu Suzuki, MD

First Department of Surgery, Hamamatsu University School of Medicine, Hamamatsu, Japan

Accepted for publication December 20, 2005.

* Address correspondence to Dr K. Suzuki, The First Department of Surgery, Hamamatsu University School of Medicine, 1-20-1 Handayama, Hamamatsu, 431-3192, Japan. (Email: kazuchi{at}fj9.so-net.ne.jp).

BACKGROUND: The presence of anomalous arch vessels has considerable impact on aortic arch reconstruction techniques and cerebral protection methods when the separated graft technique is adopted to perform total arch replacement. We analyzed our experience of total arch replacement in patients with arch vessel anomalies.

METHODS: Among the 220 patients undergoing total arch replacement at our institution, 21 patients (9.5%) had various arch vessel anomalies. Common brachiocephalic trunk was found in 8 patients (3.6%); an isolated left vertebral artery in 9 (4.1%); aberrant right subclavian artery in 3 (1.4%); and coexistent common brachiocephalic trunk and isolated left vertebral artery in 1 (0.5%). In 4 of the 9 patients with isolated left vertebral artery, preoperative diagnosis was possible with magnetic resonance angiography or three-dimensional computed tomography. In cases with common brachiocephalic trunk, total arch replacement could be performed with the usual techniques after separating the innominate and left common carotid arteries from each other. The isolated left vertebral artery was anastomosed to the left subclavian artery graft in 7 patients and to the native left subclavian artery in 2. In the aberrant right subclavian artery variety, a distal aortic anastomosis was performed distal to the orifice of this anomalous artery. The aberrant vessel was reconstructed on the right side of the trachea and esophagus.

RESULTS: There was no early or in-hospital mortality. No neurologic complication attributable to the arch vessel anomalies was found.

CONCLUSIONS: A precise preoperative diagnosis is very important for the selection of an appropriate surgical strategy in patients with arch vessel anomalies. Magnetic resonance angiography and three-dimensional computed tomography may be useful diagnostic tools in these patients.




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