Literature DB >> 17625308

Antiproteases in preventing post-ERCP acute pancreatitis.

Takeshi Tsujino1, Takao Kawabe, Masao Omata.   

Abstract

Pancreatitis remains the most common and potentially fatal complication following ERCP. Various pharmacological agents have been used in an attempt to prevent post-ERCP pancreatitis, but most randomized controlled trials have failed to demonstrate their efficacy. Antiproteases, which have been clinically used to manage acute pancreatitis, would theoretically reduce pancreatic injury after ERCP because activation of proteolytic enzymes is considered to play an important role in the pathogenesis of post-ERCP pancreatitis. Gabexate and ulinastatin have recently been evaluated regarding their efficacy in preventing post-ERCP pancreatitis. Long-term (12 hours) infusion of gabexate significantly decreased the incidence of post-ERCP pancreatitis; however, no prophylactic effect was observed for short-term infusion (2.5 and 6.5 hours). These results may be due to the short-life of gabexate (55 seconds). Since long-term infusion requires additional hospitalization, the use of gabexate in all patients at average risk of developing post-ERCP pancreatitis is an expensive strategy. Ulinastatin has a half-life of 35 minutes and can be given as a bolus infusion. Short-term (10 minutes) administration of ulinastatin showed a significant reduction in the incidence of post-ERCP pancreatitis in one randomized controlled trial. Ulinastatin is superior to gabexate in terms of cost because it does not require additional hospitalization. At present, there is no other randomized, placebo-controlled trial on ulinastatin under way. Large scale randomized controlled trials revealed that both the long-term infusion of gabexate and the short-term administration of ulinastatin may reduce pancreatic injury, but these studies involve patients at average risk of developing post-ERCP pancreatitis. Additional research is needed to confirm the preventive efficacy of these antiproteases in patients at a high risk of developing post-ERCP pancreatitis.

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Year:  2007        PMID: 17625308

Source DB:  PubMed          Journal:  JOP        ISSN: 1590-8577


  7 in total

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2.  The results of the Tokyo trial of prevention of post-ERCP pancreatitis with risperidone (Tokyo P3R): a multicenter, randomized, phase II, non-placebo-controlled trial.

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Journal:  J Gastroenterol       Date:  2012-10-24       Impact factor: 7.527

3.  Pilot study of aprepitant for prevention of post-ERCP pancreatitis in high risk patients: a phase II randomized, double-blind placebo controlled trial.

Authors:  Tilak Upendra Shah; Rodger Liddle; M Stanley Branch; Paul Jowell; Jorge Obando; Martin Poleski
Journal:  JOP       Date:  2012-09-10

4.  Urinary trypsin inhibitor attenuates lipopolysaccharide-induced neutrophil activation.

Authors:  Seong-Heon Lee; Hwi-Jin Kim; Hui-Jing Han; Mei Li; Sang-Hyun Kwak; Sanghee Park
Journal:  Korean J Anesthesiol       Date:  2012-12-14

5.  25 mg versus 50 mg dose of rectal diclofenac for prevention of post-ERCP pancreatitis in Japanese patients: a retrospective study.

Authors:  Takeo Yoshihara; Masayoshi Horimoto; Tetsuhisa Kitamura; Naoto Osugi; Tatsuro Ikezoe; Kaori Kotani; Toru Sanada; Churi Higashi; Daisuke Yamaguchi; Makiyo Ota; Tatsunori Mizuno; Yasukazu Gotoh; Yorihide Okuda; Kunio Suzuki
Journal:  BMJ Open       Date:  2015-03-20       Impact factor: 2.692

6.  The use of gabexate mesylate and ulinastatin for the prevention of post-endoscopic retrograde cholangiopancreatography pancreatitis.

Authors:  Young Wook Yoo; Sang-Woo Cha; Anna Kim; Seung Yeon Na; Young Woo Lee; Sae Hee Kim; Hyang Ie Lee; Yun Jung Lee; Hyeon Woong Yang; Sung Hee Jung
Journal:  Gut Liver       Date:  2012-04-17       Impact factor: 4.519

7.  Meta-analysis of prophylactic corticosteroid use in post-ERCP pancreatitis.

Authors:  Minghua Zheng; Jianling Bai; Bosi Yuan; Feng Lin; Jie You; Mingqin Lu; Yuewen Gong; Yongping Chen
Journal:  BMC Gastroenterol       Date:  2008-02-14       Impact factor: 3.067

  7 in total

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