AI Article Synopsis

  • A study involving 19 patients with acute pancreatitis compared high-dose octreotide treatment (9 patients) to a control group that received standard care (10 patients).
  • The octreotide group showed a significant reduction in the need for pain relief and developed fewer poor prognostic indicators after 48 hours, such as drops in hematocrit and serum albumin levels.
  • Overall, high-dose octreotide appeared to improve various measures of disease severity, suggesting it may help reduce the severity of acute pancreatitis.

Article Abstract

Nineteen consecutive patients with acute pancreatitis were sequentially allocated to treatment with high-dose octreotide (N = 9) or to act as controls (N = 10). All other aspects of treatment were similar and were according to a strict treatment protocol. There was no significant difference between the two groups on admission with regard to recognized criteria of poor prognosis. The octreotide-treated group required significantly less analgesia and after 48 hr developed significantly fewer poor prognostic indicators, including falls in hematocrit of > 10%, in serum albumin to < 32 g/liter, and in serum calcium to < 2.00 mmol/liter. Falls in arterial PO2 to < 10 kPa, in serum albumin of > 20%, and in hemoglobin of > 2 g/dl were also significantly less frequent. There was a trend towards improvement in the octreotide-treated group in every other physiological and radiological indicator of disease severity. High-dose octreotide may reduce the severity of acute pancreatitis.

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http://dx.doi.org/10.1007/BF01316794DOI Listing

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