POST-ERP PANCREATITIS AS A MODEL FOR CYTOKINE-INDUCED ACUTE-PHASE RESPONSE IN ACUTE-PANCREATITIS

Citation
H. Messmann et al., POST-ERP PANCREATITIS AS A MODEL FOR CYTOKINE-INDUCED ACUTE-PHASE RESPONSE IN ACUTE-PANCREATITIS, Gut, 40(1), 1997, pp. 80-85
Citations number
26
Categorie Soggetti
Gastroenterology & Hepatology
Journal title
GutACNP
ISSN journal
00175749
Volume
40
Issue
1
Year of publication
1997
Pages
80 - 85
Database
ISI
SICI code
0017-5749(1997)40:1<80:PPAAMF>2.0.ZU;2-8
Abstract
Background/Aims-By contrast with animal models, in most cases it is no t possible to examine the systemic response in patients in the first h ours after onset of acute pancreatitis. The aim was to determine wheth er endoscopic retrograde cholangiopancreaticography (ERP)-induced panc reatitis can be used as a human model for the study of cytokine releas e and acute phase response in the first hours of the disease. Patients and methods-Seventy consecutive patients undergoing ERP for different reasons were prospectively evaluated by sampling blood before and 0, 1, 4, 12, 24, and 48 hours after ERP and, in patients who developed an acute post-ERP pancreatitis, daily until C reactive protein (CRP) was within normal range. A post-ERP pancreatitis was defined as a threefo ld increase of amylase or lipase and at least two of the clinical symp toms: abdominal pain, nausea, vomiting, and peritonism during 24 hours after ERP. Results-Nine out of 70 patients developed an acute pancrea titis. Cytokines and other biochemical variables were measured in thos e nine and in 34 patients out of the 61 not developing pancreatitis. I n the nine patients amylase and lipase increased within the first hour after ERP with maximum values between four and 12 hours. Interleukin- 6 increased to maximal concentrations after 24-48 hours and the highes t CRP concentrations were found 72 hours after ERP. Tumour necrosis fa ctor did not change. Conclusion-Post-ERP pancreatitis is an ideal mode l in which to examine the initial cytokine and acute phase response in the first hours after the initiation of the disease.