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lüll Meta-analysis of somatostatin, octreotide and gabexate mesilate in the therapy of acute pancreatitis Andriulli A; Leandro G; Clemente R; Festa V; Caruso N; Annese V; Lezzi G; Lichino E; Bruno F; Perri FAliment Pharmacol Ther 1998[Mar]; 12 (3): 237-45BACKGROUND: Autodigestion of the pancreas, secondary to the activation of digestive enzymes, is the pathogenetic mechanism of acute pancreatitis (AP). AIM: Clinical trials in which somatostatin (SS), octreotide (OCT) and gabexate mesilate (FOY) were used to treat patients with AP, were submitted to a meta-analytical evaluation. Five end-points were evaluated: early and overall mortality, patients with complications, complication rate, and patients who needed surgery. RESULTS: In mild AP, no agent proved of value. In severe AP, both SS and OCT were beneficial in improving the overall mortality: the odds ratios (OR) were, respectively, 0.36 (95% CI: 0.20-0.64, P = 0.001) and 0.57 (95% CI: 0.35-0.88, P = 0.006). FOY had no effect on either early or overall mortality, but was effective in improving complication rate (OR = 0.70, 95% CI: 0.56-0.88, P = 0.02), number of patients with complications (OR = 0.61, 95% CI: 0.41-0.91, P = 0.01), and number of cases submitted to surgery (OR = 0.60, 95% CI: 0.39-0.92, P = 0.01). SS and OCT had no effect on these latter outcomes. CONCLUSIONS: Antisecretory agents, such as SS and OCT, are able to reduce mortality without affecting complications, whereas antiproteases, such as FOY, have no effect on mortality but do reduce complications. A trial exploring the efficacy of combining antisecretory agents with antiproteases would be of great benefit in patients with severe AP.|Acute Disease[MESH]|Anticoagulants/*therapeutic use[MESH]|Clinical Trials as Topic[MESH]|Gabexate/*therapeutic use[MESH]|Hormone Antagonists/*therapeutic use[MESH]|Hormones/*therapeutic use[MESH]|Humans[MESH]|Octreotide/*therapeutic use[MESH]|Pancreatitis/*drug therapy[MESH]|Somatostatin/*therapeutic use[MESH]|Statistics as Topic[MESH]|Treatment Outcome[MESH] |