Vascular access and contrast media.
J Infus Nurs. 2011 Mar-Apr;34(2):97-105
Authors: Earhart A, McMahon P
Over the past several years, the Food and Drug Administration (FDA) has received more than 250 adverse event reports in which vascular access devices have ruptured when used with power injectors. The adverse events include rupture and device fragmentation. The outcome of these events affects both the patient and the care provider.
PMID: 21399455 [PubMed - indexed for MEDLINE]