A prospective study of prophylactic long-acting octreotide in high-risk patients undergoing pancreaticoduodenectomy

Am J Surg. 2011 Apr;201(4):481-5. doi: 10.1016/j.amjsurg.2010.06.038.

Abstract

Background: Postoperative pancreatic fistula (postoperative pancreatic fistula [POPF]) is the most common complication after pancreaticoduodenectomy. Despite some studies showing little effect of octreotide in unselected patients, we hypothesized that in high-risk patients depot octreotide may reduce the risk of POPF.

Methods: Sixty-eight patients were prospectively evaluated for inclusion in the current study. Two groups were identified: pancreatic ducts ≤3 mm (high risk) and those with ducts >3 mm (low risk). Thirty-two patients were low risk, whereas 36 patients were high risk. High-risk patients were treated preoperatively with depot octreotide and begun on an intravenous drip for 24 hours. Low-risk patients underwent pancreaticoduodenectomy without pharmacologic intervention. In contrast, the control cohort represents 106 retrospectively analyzed patients who underwent a pancreaticoduodenectomy without depot octreotide injection without regard to low- or high-risk status.

Results: Overall, POPF was 11 of 68 (16%). Nine of 36 high risk patients treated with depot octreotide developed POPF (25%), and 2 of 32 low risk patients developed POPF (6%). In the control cohort of high-risk patients, 9 of 44 (20%) and 3 of 62 (5%) low-risk patients developed POPF (P = .628 when comparing the development of POPF in high-risk patients with or without pharmacologic intervention).

Conclusions: Prophylactic use of depot octreotide in high-risk patients does not result in reduced incidence of POPF. Duct size has a significant impact on the occurrence of POPF.

MeSH terms

  • Delayed-Action Preparations / therapeutic use
  • Gastrointestinal Agents / therapeutic use*
  • Humans
  • Octreotide / therapeutic use*
  • Pancreatic Fistula / epidemiology
  • Pancreatic Fistula / prevention & control*
  • Pancreaticoduodenectomy / adverse effects*
  • Premedication*
  • Prospective Studies
  • Retrospective Studies
  • Risk Assessment
  • Treatment Outcome

Substances

  • Delayed-Action Preparations
  • Gastrointestinal Agents
  • Octreotide