Endoscopy 1988; 20: 179-183
DOI: 10.1055/s-2007-1018172
© Georg Thieme Verlag KG Stuttgart · New York

Biliary Dyskinesia

W. J. Hogan1 , J. E. Geenen2
  • 1Professor of Medicine, Director, GI Diagnostic Labs, Medical College of Wisconsin, Milwaukee, Wisconsin
  • 2Clinical Professor of Medicine, Medical College of Wisconsin, Milwaukee, Wisconin, Director, Digestive Disease Center St. Luke's Hospital, Racine, Wisconsin
Further Information

Publication History

Publication Date:
17 March 2008 (online)

Summary

Delivery of bile into the duodenum involves a series of complex interrelationships between hepatic secretion of bile and pressure differentials generated within the gallbladder, cystic duct and sphincter of Oddi. Theoretically, functional disorders of bile flow may arise from a disturbance of any one of the above factors. A brief review of our present knowledge of the physiology of bile flow and the spectrum of functional biliary tract disorders will be outlined to help explain possible factors which may be involved in biliary tract dysmotility disturbances.

The sphincter of Oddi (SO) mechanism is dedicated to maintaining a low pressure system within the hepatic ducts which allows hepatic secretion to proceed irrespective of bile flow rate. Partial obstruction at the SO segment can give rise to intermittent or persistent upper abdominal pain.

We classify sphincter of Oddi (SO) motor dysfunction into two broad categories: 1. SO stenosis: defined as a structural narrowing of part or all of the SO segment, and 2) SO dyskinesia: defined as a primary disorder of SO tonic/phasic motor activity. We have attempted to deal with an overlap in etiology of SO motor dysfunction by developing patient group classifications. Biliary I-patients with biliary-type pain, abnormal liver function tests (SGOT; al PO4 > 2 × normal) documented on 2 or more occasions, delayed drainage of ERCP contrast > 45 min, and dilated CBD > 12 mm diameter; Biliary II-patients with biliary-type pain but only 1 or 2 of the above criteria; Biliary III-patients with only biliary-type pain and no other abnormalities. A few of these patients may have primary SO dyskinasia.

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