Ulinastatin shows preventive effect on post-endoscopic retrograde cholangiopancreatography pancreatitis in a multicenter prospective randomized study

被引:68
作者
Fujishiro, Hirofumi
Adachi, Kyoichi
Imaoka, Tomonori
Hashimoto, Tomoyuki
Kohge, Naruaki
Moriyama, Nobuyuki
Suetsugu, Hiroshi
Kawashima, Kousaku
Komazawa, Yoshinori
Ishimura, Norihisa
Ishihara, Shunji
Amano, Yuji
Kinoshita, Yoshikazu
机构
[1] Shimane Med Univ, Sch Med, Dept Gastroenterol & Hepatol, Izumo, Shimane 6938501, Japan
[2] Shimane Prefectural Cent Hosp, Dept Gastrointestinal Dis, Izumo, Shimane, Japan
[3] Unnan Gen Hosp, Dept Internal Med, Unnan, Japan
关键词
endoscopic retrograde cholangiopancreatography; gabexate mesilate; pancreatitis; ulinastatin;
D O I
10.1111/j.1440-1746.2006.04085.x
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background and Aim: Endoscopic retrograde cholangiopancreatography (ERCP) is a useful diagnostic and therapeutic procedure; however, ERCP occasionally causes post-ERCP pancreatitis. The administration of gabexate mesilate has been reported to be effective for the prevention for post-ERCP pancreatitis when given during and after the procedure. The aim of the present study was to investigate the preventive effect of the novel protease inhibitor ulinastatin on post-ERCP pancreatitis. Methods: One hundred and thirty-nine patients who underwent the ERCP procedure were studied. These patients were randomly divided into three groups based on the agent and dose given during and following the ERCP procedure: gabexate mesilate (900 mg), high-dose ulinastatin (450 000 units) and low-dose ulinastatin (150 000 units). Serum amylase, interleukin (IL)-6 and IL-8 levels and plasma polymorphonuclear leukocyte elastase (PMN-E) activity were measured after ERCP. In addition, post-ERCP hyperamylasemia and post-ERCP pancreatitis were recorded. Results: There were no significant differences in serum amylase, IL-6 and IL-8 levels and PMN-E activity after ERCP procedure between the three groups. Post-ERCP pancreatitis was observed in two (4.3%), three (6.5%) and four (8.5%) cases in the gabexate mesilate, high-dose ulinastatin and low-dose ulinastatin groups, respectively. Multiple logistic regression analysis showed that the addition of endoscopic sphincterotomy during the ERCP procedure was the only significant risk factor for the development of post-ERCP hyperamylasemia and post-ERCP pancreatitis (P = 0.03 and P = 0.04, respectively), but there was no significant difference in the occurrence of post-ERCP hyperamylasemia and post-ERCP pancreatitis between the three groups receiving different preventative treatments. Conclusion: The administration of low- and high-dose ulinastatin has similar effects to high-dose gabexate in the prevention of post-ERCP pancreatitis. (c) 2006 Blackwell Publishing Asia Pty Ltd.
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页码:1065 / 1069
页数:5
相关论文
共 34 条
[1]
Mechanism of pancreatitis caused by ERCP [J].
Akashi, R ;
Kiyozumi, T ;
Tanaka, T ;
Sakurai, K ;
Oda, Y ;
Sagara, K .
GASTROINTESTINAL ENDOSCOPY, 2002, 55 (01) :50-54
[2]
Gabexate or somatostatin administration before ERCP in patients at high risk for post-ERCP pancreatitis: a multicenter, placebo-controlled, randomized clinical trial [J].
Andriulli, A ;
Clemente, R ;
Solmi, L ;
Terruzzi, V ;
Suriani, R ;
Sigillito, A ;
Leandro, G ;
Leo, P ;
De Maio, G ;
Perri, F .
GASTROINTESTINAL ENDOSCOPY, 2002, 56 (04) :488-495
[3]
Pharmacologic treatment can prevent pancreatic injury after ERCP: a meta-analysis [J].
Andriulli, A ;
Leandro, G ;
Niro, G ;
Mangia, A ;
Festa, V ;
Gambassi, G ;
Villani, MR ;
Facciorusso, D ;
Conoscitore, P ;
Spirito, F ;
De Maio, G .
GASTROINTESTINAL ENDOSCOPY, 2000, 51 (01) :1-7
[4]
A prospective, randomized, placebo-controlled trial of prednisone and allopurinol in the prevention of ERCP-induced pancreatitis [J].
Budzynska, A ;
Marek, T ;
Nowak, A ;
Kaczor, R ;
Nowakovska-Dulawa, E .
ENDOSCOPY, 2001, 33 (09) :766-772
[5]
Gabexate for the prevention of pancreatic damage related to endoscopic retrograde cholangiopancreatography [J].
Cavallini, G ;
Tittobello, A ;
Frulloni, L ;
Masci, E ;
Mariani, A ;
DiFrancesco, V ;
Angelini, GP ;
Casarini, MB ;
Bedogni, G ;
Conigliaro, R ;
Bonardi, L ;
Khajekini, MTA ;
Cipolletta, L ;
Bianco, MA ;
Costamagna, G ;
Perri, V ;
Dobrilla, G ;
DePretis, G ;
Familiari, L ;
Giacobbe, G ;
Fratton, A ;
Carone, N ;
Loriga, P ;
Muscas, A ;
Mazzeo, F ;
Gaeta, L ;
Miglioli, M ;
Pezzilli, R ;
Morelli, A ;
Santucci, L ;
Naccarato, R ;
DelFavero, G ;
Orlandi, F ;
Macarri, GP ;
Russo, A ;
Virgilio, C ;
Uomo, G ;
Manes, G .
NEW ENGLAND JOURNAL OF MEDICINE, 1996, 335 (13) :919-923
[6]
Post-ERCP pancreatitis and hyperamylasemia: Patient-related and operative risk factors [J].
Christoforidis, E ;
Goulimaris, I ;
Kanellos, I ;
Tsalis, K ;
Demetriades, C ;
Betsis, D .
ENDOSCOPY, 2002, 34 (04) :286-292
[7]
Selective cannulation of the common bile duct: a prospective randomized trial comparing standard catheters with sphincterotomes [J].
Cortas, GA ;
Mehta, SN ;
Abraham, NS ;
Barkun, AN .
GASTROINTESTINAL ENDOSCOPY, 1999, 50 (06) :775-779
[8]
ENDOSCOPIC SPHINCTEROTOMY COMPLICATIONS AND THEIR MANAGEMENT - AN ATTEMPT AT CONSENSUS [J].
COTTON, PB ;
LEHMAN, G ;
VENNES, J ;
GEENEN, JE ;
RUSSELL, RCG ;
MEYERS, WC ;
LIGUORY, C ;
NICKL, N .
GASTROINTESTINAL ENDOSCOPY, 1991, 37 (03) :383-393
[9]
Proinflammatory cytokine release by peripheral blood mononuclear cells from patients with acute pancreatitis [J].
deBeaux, AC ;
Ross, JA ;
Maingay, JP ;
Fearon, JP ;
Fearon, KCH ;
Carter, DC .
BRITISH JOURNAL OF SURGERY, 1996, 83 (08) :1071-1075
[10]
ENDO S, 1990, CLIN THER, V12, P323