ACG Clinical Guideline: Primary Sclerosing Cholangitis

Am J Gastroenterol. 2015 May;110(5):646-59; quiz 660. doi: 10.1038/ajg.2015.112. Epub 2015 Apr 14.

Abstract

Primary sclerosing cholangitis is a chronic cholestatic liver disease that can shorten life and may require liver transplantation. The cause is unknown, although it is commonly associated with colitis. There is no approved or proven therapy, although ursodeoxycholic acid is used by many on an empiric basis. Complications including portal hypertension, fat-soluble vitamin deficiency, metabolic bone diseases, and development of cancers of the bile duct or colon can occur.

Publication types

  • Practice Guideline

MeSH terms

  • Anti-Infective Agents / therapeutic use
  • Cholagogues and Choleretics / therapeutic use
  • Cholangiopancreatography, Endoscopic Retrograde*
  • Cholangitis, Sclerosing / complications
  • Cholangitis, Sclerosing / diagnosis*
  • Cholangitis, Sclerosing / epidemiology
  • Cholangitis, Sclerosing / therapy*
  • Digestive System Neoplasms / diagnosis*
  • Gallstones
  • Humans
  • Immunosuppressive Agents / therapeutic use
  • Inflammatory Bowel Diseases / diagnosis*
  • Inflammatory Bowel Diseases / epidemiology
  • Liver Transplantation
  • Ursodeoxycholic Acid / therapeutic use

Substances

  • Anti-Infective Agents
  • Cholagogues and Choleretics
  • Immunosuppressive Agents
  • Ursodeoxycholic Acid