Acute pancreatitis is caused by the activation of digestive enzymes in
the pancreas and a possible treatment, therefore, is the inhibition o
f enzyme secretion. This approach is somewhat controversial, however,
as it is not clear whether pancreatic secretion continues to occur dur
ing the course of acute pancreatitis. Animal studies show an appreciab
le reduction of secretion in the inflamed pancreas, but studies in hum
ans are not conclusive. The use of somatostatin or its analogue, octre
otide, has been investigated in several clinical studies. A meta analy
sis of six individual studies in which somatostatin was given for acut
e pancreatitis showed that somatostatin significantly reduces mortalit
y. A trial in patients with moderate to severe acute pancreatitis show
ed a lower rate (although not statistically significant) of complicati
ons in patients treated with 3 X 200 and 3 X 500 mu g/day octreotide,
compared with controls and patients receiving a lower dose of octreoti
de. A further study showed a significant reduction in patient controll
ed analgesics in patients treated with octreotide compared with contro
ls. Pain is the important clinical symptom of chronic pancreatitis, po
ssibly resulting fi om an increased intraductal pressure during secret
ion. The effect on pain of the inhibition of pancreatic secretion by o
ctreotide has been investigated in two studies. One showed no signific
ant reduction in pain after treatment with octreotide for three days.
In the other, in which octreotide was used for three weeks, significan
tly less pain and analgesic use was recorded during octreotide treatme
nt than during placebo. The most common complication of chronic pancre
atitis is the formation of pseudocysts. There is some evidence that oc
treotide may be useful in their treatment.