Complications of arterial closure devices
As of July 2000, there were 4 closure devices with Food and Drug Administration (FDA) approval. The devices are successfully deployed in 89% to 98% of cases, and the complication rates are comparable to those seen with manual compression. Minor access site complications are defined as bleeding not r...
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Veröffentlicht in: | Techniques in vascular and interventional radiology 2003-06, Vol.6 (2), p.103-106 |
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Sprache: | eng |
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