3.9 Article

Therapeutic endovascular treatments for traumatic carotid artery injuries

Journal

JOURNAL OF TRAUMA-INJURY INFECTION AND CRITICAL CARE
Volume 58, Issue 6, Pages 1159-1166

Publisher

LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1097/01.TA.0000171550.01402.ED

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Objective: The diagnosis and management of traumatic carotid vessel injuries continue to be controversial, with direct surgical repair with parent artery preservation still presenting difficulties. The purpose of this report is to review the endovascular therapy of patients with traumatic carotid vessel injuries for preservation of the parent artery, and to determine the safety and efficacy of endovascular therapy. Methods: Ten patients with traumatic carotid lesions were treated using therapeutic endovascular methods. Endovascular therapy was accomplished by implanting balloons, porous or polytetraflu-oroethylene-covered stents, and/or embolic materials including coils or glue. Results: All fistulas and pseudoaneurysms were successfully embolized with no periprocedural complications including vessel disruption/rupture, distal embolization, or new neurologic deficits. The parent arteries of all patients except one were preserved. The reason for the parent artery sacrifice was a thrombus formation due to coil migration into the parent artery. No additional surgical procedures for vascular lesions were required. There were no delayed neurologic or vascular complications, and no lesions recurred during the follow-up periods (mean 203 months). Conclusion: The goal of endovascular therapy is the selective elimination of the vascular pathology with the normal patency of the cerebral arteries. The authors' experience demonstrates that endovascular therapy using stents, balloons, and coils is both feasible and safe for treatment of traumatic carotid injuries. Of these endovascular methods, the stent can be used to exclude the aneurysm or fistula from the circulation and preserve the parent artery in selective cases. Longterm follow-up review of these repairs will be necessary to provide a full evaluation of the safety and efficacy of these devices.

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