Frequency of pancreatitis after endoscopic retrograde cholangiopancreatography with iopromid or iotrolan: a randomized trial

Citation
C. Goebel et al., Frequency of pancreatitis after endoscopic retrograde cholangiopancreatography with iopromid or iotrolan: a randomized trial, EUR RADIOL, 10(4), 2000, pp. 677-680
Citations number
22
Categorie Soggetti
Radiology ,Nuclear Medicine & Imaging
Journal title
EUROPEAN RADIOLOGY
ISSN journal
09387994 → ACNP
Volume
10
Issue
4
Year of publication
2000
Pages
677 - 680
Database
ISI
SICI code
0938-7994(2000)10:4<677:FOPAER>2.0.ZU;2-3
Abstract
Blood isotone contrast media is-considered to be less toxic to vascular and pancreatic duct endothelium than high-osmolar contrast media. In this stud y we assessed the impact of a low-osmolar contrast agent compared with a bl ood isotone product on pancreatic damage induced by endoscopic retrograde c holangiopancreatography (ERCP) and endoscopic retrograde sphincterotomy (ES T). In a prospective trial 42 consecutive ERCP/EST patients were randomized to receive either iopromid, a low-osmolar non-ionic contrast agent (770 mo smol/kg H2O), or iotrolan, a blood-isotone non-ionic product (320 mosmol/kg H2O). The endoscopies were performed by two experienced endoscopists. Fort y patients were included in the study. Blood samples were collected before and 40 min, 2, 4, 6 and 24 h after the endoscopic procedure. Samples were a nalysed for pancreatic serum enzymes, acute-phase proteins and blood counts . A clinical pain score was investisgated. Post-ERCP pancreatitis was diagn osed in 2 patients in the iopromid group and in 5 patients in the iotrolan group. There was no significant difference between groups in the time cours e of pancreatic serum enzymes, acute-phase proteins or in the pain score. D ue to the small number of patients in this study, only stronger differences caused by the two contrast media could have led to statistically significa nt results. We did not observe statistically significant differences in com paring iotrolan and iopromid concerning ERCP/EST-induced pancreatic damage.