Primary biliary cholangitis: assessment and management strategies

Author:

Abbas S Nadir1,Jones David2,Kallis Yiannis3,Maher Laura4,Patanwala Imran5

Affiliation:

1. Specialist Registrar in Gastroenterology and Research, Fellow in Hepatology, Liver Unit, Queen Elizabeth Hospital, Birmingham and Department of Immunology, University of Birmingham

2. Professor of Liver Immunology, Newcastle University

3. Consultant Hepatologist and Gastroenterologist, and Honorary Senior Lecturer, Barts and the London, School of Medicine and Dentistry, Queen Mary University of London

4. Advanced Nurse Specialist Hepatology, Hepatology, Non-medical Prescibing, York Teaching Hospital NHS Foundation Trust

5. Consultant Gastroenterologist and Hepatologist, Liverpool University Hospitals NHS Foundation Trust

Abstract

Primary biliary cholangitis (PBC) is an autoimmune disease resulting in permanent damage to the bile ducts in the liver, often leading to symptoms including fatigue and itch that significantly impair patient quality of life. PBC is often diagnosed in its early stages and can generally be treated effectively with first-line treatment. Patients who do not respond to this should be referred to the hub centre of their local operational delivery network for assessment and prescription of second-line treatment. These patient treatment pathways are based on national guidance. This supplement summarises the key components of the guidance on the assessment, diagnosis and treatment of patients with PBC.

Publisher

Mark Allen Group

Subject

Advanced and Specialized Nursing,Medical–Surgical Nursing

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