Hepatic Failure/GI/Endocrine Emergencies
Somatostatin significantly reduces output volumes. One prospective, randomized controlled
single-center trial compared somatostatin 250 mcg/hour intravenously continuously with placebo
for patients receiving TPN. Somatostatin significantly reduced the time to achieve a 50%, 75%, and
100% reduction in fistula output compared with placebo; also, although there was no difference in
the rates of fistula closure (85% vs. 81.25%), the time to fistula closure was significantly reduced
with the use of somatostatin (13.9 days vs. 20.4 days, p<0.05).
| d. | Octreotide has been shown to decrease fistula output in some studies, though in other trials, it had |
|---|
no effect on fistula output.
One small study of 14 patients showed a beneficial effect of octreotide on output volumes.
In this crossover study, octreotide at 100 mcg subcutaneously three times daily significantly
reduced fistula output compared with placebo for the first 2 days of therapy by about 400 mL/
day. When the group that was originally randomized to receive octreotide crossed over to the
placebo arm, output increased by about 250 mL/day.
ii.
Two subsequent studies did not show similar results on fistula output. Possible reasons for
decreased efficacy with octreotide include diminished response with repeat dosing and
decreased activity at some somatostatin receptors.
Reduction in fistula output with the use of somatostatin or octreotide should occur within 48 hours.
If no noticeable response in fistula response occurs at 48 hours, treatment should be discontinued.
Refractory high-output fistula management
Acid-suppressing medications (e.g., PPIs and histamine-2 receptor antagonists) have been studied
for the treatment of refractory fistula because of their ability to decrease gastric acidity and decrease
the amount of gastric secretions. Proton pump inhibitors are more effective than histamine-2
receptor antagonists for refractory fistula output.
Antimotility agents are usually recommended (e.g., loperamide, diphenoxylate/atropine, codeine)
because of their ability to inhibit the activity of gastrointestinal tract muscles.
Loperamide has the greatest effect on fistula output. In studies, loperamide doses up to 12β24
mg per dose have been given safely for the management of high-output fistulas. However, due
to concerns for adverse reactions, caution should be advised with doses higher than 16 mg
per day. Additionally, administration of large quantities of the liquid form of loperamide may
increase fistula output.
Conservative versus surgical management
Conservative management is first line for most patients, with the primary goal being spontaneous
closure of the fistula. Several prognostic indicators improve the likelihood of spontaneous closure.
Low-output fistulas
ii.
Patients younger than 40 years
iii.
Fistula sites: Oropharyngeal, esophageal, duodenal, pancreatic, jejunal
iv.
A long fistula tract (greater than 2 cm)
Intestinal continuity maintained
Surgery is usually indicated for fistulas that fail to close spontaneously after 30β60 days. Some
causes of fistula formation (e.g., bowel injury caused by trauma or certain surgical procedures) may
require emergency surgery to repair damage.