Natural history of primary biliary cirrhosis

Clin Liver Dis. 2008 May;12(2):277-88; viii. doi: 10.1016/j.cld.2008.02.012.

Abstract

Primary biliary cirrhosis is an insidious disease that progresses through the clinical phases: preclinical, asymptomatic, symptomatic, and liver insufficiency. The outlook of patients diagnosed with PBC has improved significantly over the past 2 decades because more patients are being diagnosed earlier in the disease process and being treated with UDCA. A need remains to better define and predict the course of symptomatic and asymptomatic patients on and off UDCA in order to better evaluate outcomes of clinical trials.

Publication types

  • Review

MeSH terms

  • Cholagogues and Choleretics / therapeutic use
  • Humans
  • Liver Cirrhosis, Biliary / complications*
  • Liver Cirrhosis, Biliary / pathology*
  • Liver Cirrhosis, Biliary / therapy
  • Ursodeoxycholic Acid / therapeutic use

Substances

  • Cholagogues and Choleretics
  • Ursodeoxycholic Acid