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Somatostatin analogues in the prevention of pancreas‐related complications after pancreatic resection
Author(s) -
Medina Antonio RamosDe la,
Sarr Michael G.
Publication year - 2006
Publication title -
journal of hepato‐biliary‐pancreatic surgery
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.63
H-Index - 60
eISSN - 1868-6982
pISSN - 0944-1166
DOI - 10.1007/s00534-005-1033-9
Subject(s) - medicine , perioperative , somatostatin , pancreatitis , pancreas , pancreatectomy , placebo , surgery , gastroenterology , randomized controlled trial , pancreatic disease , prospective cohort study , pathology , alternative medicine
Background/Purpose The Achilles' heel of operative pancreatectomies is the pancreaticoenterostomy for proximal resections and the pancreatic parenchymal closure for distal resections. Inhibition of pancreatic exocrine secretions by somatostatin analogues has been suggested to decrease pancreas‐specific complications, but this topic remains controversial. Methods We performed a randomized, prospective, placebo‐controlled, multicenter trial of the use of perioperative vapreotide, a potent somatostatin analogue, in pancreatic resections for presumed neoplasms in 381 patients without chronic pancreatitis. We also reviewed the literature on the use of somatostatin and its analogues after pancreatectomy. Results When compared to the placebo, perioperative vapreotide had no effect on overall pancreas‐specific complications (30.4% vs 26.4%), mortality (0% vs 1.4%), overall complications (40% vs 42%), and duration of hospitalization; there were no differences in complications per type of resection with use of vapreotide — proximal versus distal resection. Seven other prospective, randomized trials provide differing results. Conclusions Our study with vapreotide failed to show any benefit when administered perioperatively (and for 7 days postoperatively) on pancreas‐specific complications after major pancreatectomy in patients without chronic pancreatitis. The use of perioperative analogues that suppress pancreatic exocrine secretion seems not to be warranted as routine treatment.