Complications associated with percutaneous closure devices - 08/09/11
Abstract |
Background: In an effort to reduce time to hemostasis after angiography, several closure devices have been marketed. We report some of their complications.
Methods: A retrospective review was conducted.
Results: Over an 8-month study period, 2,181 diagnostic and interventional procedures were performed. Closure devices were used in 408 (19%) of these patients. The Angio-Seal closure device is composed of a collagen sponge and an absorbable polymer anchor that compresses the hole in the arteriotomy. The ProstarXL sealing device consists of a rotating barrel that deploys 4 needles through the arteriotomy, and then individual knots are extracorporeally tied. The Duett device consists of a balloon occluding catheter and injectable collagen and thrombin. Ten of the patients developed a complication from the closure device (2.5%). Four of these were subcutaneous abscesses. Two of these patients had expanding pseudaneurysms, 2 had lower extremity ischemia, and 1 patient had an acute bleed. These complications were all managed surgically. Another patient developed a retroperitoneal bleed that was managed nonoperatively.
Conclusions: As the use of these devices increase, these complications will become more common.
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Vol 178 - N° 3
P. 209-211 - septembre 1999 Retour au numéroBienvenue sur EM-consulte, la référence des professionnels de santé.
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