Gabexate for the Prevention of Pancreatic Damage Related to Endoscopic Retrograde Cholangiopancreatography
Giorgio Cavallini, M.D., Alberto Tittobello, M.D., Luca Frulloni, M.D., Enzo Masci, M.D., Alberto Mariani, M.D., Vincenzo Di Francesco, M.D., for The Gabexate in Digestive Endoscopy Italian Group
Background Endoscopic retrograde cholangiopancreatography (ERCP)is associated with elevated levels of pancreatic enzymes andpancreatitis. Gabexate, a protease inhibitor, has been usedto prevent pancreatic damage related to ERCP.
Methods We conducted a multicenter, double-blind comparisonof gabexate (1 g given by intravenous infusion starting 30 to90 minutes before endoscopy and continuing for 12 hours afterward)with placebo (mannitol and sodium chloride, administered inthe same fashion). A total of 435 adults scheduled to undergoERCP and, when indicated, endoscopic sphincterotomy underwentrandomization; 17 were excluded from the final analysis forvarious reasons. The remaining 418 patients (mean age, 60.4years) 208 in the gabexate group and 210 in the placebogroup were analyzed. Acute pancreatitis was consideredto be present if serum amylase or lipase levels (or both) werefive times greater than the upper limits of normal in associationwith the onset of pancreatic pain.
Results After the procedures, 276 patients (66 percent) hadelevated pancreatic-enzyme levels; the frequency was similarin the two groups. Mean serum amylase values were higher inthe placebo group than in the gabexate group through 24 hoursof observation (P = 0.03). Twelve patients in the gabexate groupand 29 in the placebo group had abdominal pain (6 percent vs.14 percent, P = 0.009). Sixteen patients in the placebo groupand five in the gabexate group had acute pancreatitis (8 percentvs. 2 percent, P = 0.03). Two patients treated with gabexateand six given placebo had adverse events, all of which resolved.Two patients given placebo died of acute pancreatitis; one wasexcluded from the evaluation because pancreatitis was presentbefore endoscopy. One patient in the gabexate group died, froma myocardial infarction.
Conclusions Prophylactic treatment with gabexate reduced pancreaticdamage related to ERCP, as reflected by reductions in the extentbut not the frequency of elevated enzyme levels and in the frequencyof pancreatic pain and acute pancreatitis.
Source Information
From the Cattedra di Gastroenterologia, Università di Verona, Verona (G.C., L.F., V.D.F.); and Servizio di Gastroenterologia ed Endoscopia Digestiva, Ospedale S. Raffaele, Milan (A.T., E.M., A.M.) both in Italy.
Address reprint requests to Dr. Cavallini at the Cattedra di Gastroenterologia, Policlinico Borgo Roma, via delle Menegone, 37134 Verona, Italy.
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