POST-ERCP PANCREATITIS - RANDOMIZED, PROSPECTIVE-STUDY COMPARING A LOW-OSMOLALITY AND HIGH-OSMOLALITY CONTRAST AGENT

Citation
S. Sherman et al., POST-ERCP PANCREATITIS - RANDOMIZED, PROSPECTIVE-STUDY COMPARING A LOW-OSMOLALITY AND HIGH-OSMOLALITY CONTRAST AGENT, Gastrointestinal endoscopy, 40(4), 1994, pp. 422-427
Citations number
23
Categorie Soggetti
Gastroenterology & Hepatology
Journal title
ISSN journal
00165107
Volume
40
Issue
4
Year of publication
1994
Pages
422 - 427
Database
ISI
SICI code
0016-5107(1994)40:4<422:PP-RPC>2.0.ZU;2-1
Abstract
Diagnostic and therapeutic ERCPs are complicated by pancreatitis in 1% to 10% of patients, and evidence suggests that the contrast agent use d for ERCP may be important in the pathogenesis of such pancreatitis. This prospective, double-blind study was undertaken to determine wheth er the use of a low-osmolality, nonionic contrast agent (Omnipaque 300 ; iohexol, 672 mOsm/kg H2O) would reduce the frequency and severity of postprocedure pancreatitis as compared to a high-osmolality, ionic co ntrast agent (Hypaque 50%; diatrizoate sodium, 1515 mOsm/kg H2O). Six hundred ninety patients undergoing diagnostic ERCP (pancreatogram, cho langiogram, or both) either with or without sphincter of Oddi manometr y and therapy were randomized to iohexol or diatrizoate sodium. Postpr ocedure pancreatitis was diagnosed when the serum amylase or lipase le vel wits elevated to at least four times the upper limits of normal at 18 hours and was associated with increased abdominal pain persisting for at least 24 hours after the procedure that required administration of narcotic analgesics. The pancreatitis was graded as mild, moderate , or severe depending on the length of hospital stay and the need for intervention. The overall frequency (7.2% versus 7.5%) and severity (4 .3% mild, 2% moderate, 0.9% severe for the diatrizoate sodium group ve rsus 4.3% mild, 2.6% moderate, and 0.6% severe for the iohexol group) of postprocedure pancreatitis and the frequency and severity within ea ch procedure category were similar for the two contrast agent groups ( p > .05). Similarly, no statistical difference was noted (p > .05) in the incidence and severity of postprocedure pancreatitis for the two c ontrast agent groups when the data were analyzed for patients who had had a pancreatogram (8.8% versus 9%). In conclusion, the incidence and severity of postprocedure pancreatitis is not altered by the use of i ohexol. In view of the relatively high cost of this agent, its routine use for ERCP is not recommended.