PURPOSE: To determine the safety and diagnostic accuracy of a provocat
ive protocol with heparin and urokinase to induce bleeding and determi
ne the source in patients with chronic gastrointestinal hemorrhage. MA
TERIALS AND METHODS: Nine patients had gastrointestinal bleeding from
an indeterminate source and had negative results from esophagogastrodu
odenoscopy, colonoscopy, small-bowel examination, and angiography. Ten
provocative bleeding studies were performed prospectively. Patients h
ad no clinical evidence of bleeding within 2 days before the study. In
travenous administration of heparin and urokinase was performed system
ically during a 4-hour period while scintigraphy was performed continu
ously. Mesenteric angiography was performed immediately in patients in
whom substantial gastrointestinal bleeding was detected at scintigrap
hy. RESULTS: The provocative protocol was successful in inducing scint
igraphically detectable hemorrhage in four (40%) studies within 4 hour
s. In two of these four studies, the source of hemorrhage was determin
ed and treated with embolization or surgery. Three (30%) studies demon
strated scintigraphic evidence of hemorrhage only at delayed imaging (
8-24 hours after initiation of the study). The remaining three (30%) s
tudies did not show active bleeding. No complications occurred, includ
ing hemodynamic instability or uncontrollable decreases in hematocrit.
CONCLUSION: Since this protocol with heparin and urokinase enabled de
termination of the bleeding source in only two of 10 studies, protocol
modifications are necessary before this intervention is used widely.