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High-dose allopurinol for prevention of post-ERCP pancreatitis: a prospective randomized double-blind controlled trial
- Source :
- Gastrointestinal Endoscopy. 61:407-415
- Publication Year :
- 2005
- Publisher :
- Elsevier BV, 2005.
-
Abstract
- Pancreatitis is the most common major complication of diagnostic and therapeutic ERCP. Allopurinol, a xanthine oxidase inhibitor that blocks generation of oxygen-derived free radicals, potentially may prevent post-ERCP pancreatitis. This study assessed the efficacy of high-dose oral allopurinol for prevention of post-ERCP pancreatitis.A prospective, double-blind, placebo-controlled trial was conducted in 250 patients undergoing ERCP. Patients were randomized to receive allopurinol (600 mg) or placebo orally at 15 and 3 hours before the procedure. Patients were clinically evaluated, and serum amylase levels were determined before ERCP and at 6 and 24 hours thereafter. Standardized criteria were used to diagnose and to grade the severity of post-ERCP pancreatitis.A total of 243 patients were included in the analysis. The two groups were similar with regard to age; gender; underlying disease; indication for treatment; ERCP findings; and type of treatment, except for biliary sphincterotomy. Only 43 patients in the allopurinol group underwent biliary sphincterotomy vs. 87 in the placebo group ( p0.001). The frequency of acute pancreatitis was significantly lower in the allopurinol vs. the placebo group in the final multinomial regression analysis: allopurinol group, 4/125 (3.2%), with all 4 cases graded as mild, vs. placebo group, 21/118 (17.8%), of which 8/118 (6.8%) were graded as mild, 11/118 (9.3%) as moderate, and 2/118 (1.6%) as severe with fatal outcome ( p0.001). The protective effect of allopurinol was also apparent in the diagnostic ERCP and the biliary sphincterotomy subgroups when the frequency of post-ERCP pancreatitis was analyzed after stratification by procedure. The mean duration of hospitalization for pancreatitis was significantly shorter in the allopurinol compared with the placebo group (2.5 vs. 5.67 days; p0.001).Pretreatment with high-dose, orally administered allopurinol decreases the frequency of post-ERCP pancreatitis. Despite the promising results of this prospective, randomized trial, further studies are needed to verify these observations before allopurinol can be recommended for routine clinical use.
- Subjects :
- Adult
Male
medicine.medical_specialty
Pancreatic disease
medicine.drug_class
Allopurinol
Placebo
Gastroenterology
law.invention
Double-Blind Method
Randomized controlled trial
law
Internal medicine
medicine
Humans
Radiology, Nuclear Medicine and imaging
Prospective Studies
Prospective cohort study
Xanthine oxidase inhibitor
Aged
Aged, 80 and over
Cholangiopancreatography, Endoscopic Retrograde
business.industry
Free Radical Scavengers
Middle Aged
medicine.disease
digestive system diseases
Surgery
Clinical trial
surgical procedures, operative
Pancreatitis
Female
business
medicine.drug
Subjects
Details
- ISSN :
- 00165107
- Volume :
- 61
- Database :
- OpenAIRE
- Journal :
- Gastrointestinal Endoscopy
- Accession number :
- edsair.doi.dedup.....36296c3a9c3726cc2fc31081e92a6659
- Full Text :
- https://doi.org/10.1016/s0016-5107(04)02647-1