Cholestatic Liver Disease: Lived Experience Influencing Care Pathways

Description

Developed by Patient Advisory Group, this session examines the importance of the patient experience within research and clinical care with a focus on cholestatic liver disease—especially primary sclerosing cholangitis (PSC). Session themes include issues of delayed diagnosis, fragmented care, unmet symptom burdens, and ways to improve the patient experience through better care coordination.

Presentations

11:05 AM - 11:15 AM
Convention Center - Mile High Ballroom 4DEF

Overview of Unmet Needs in Cholestatic Liver Disease: Patient Pathways/The Journey From Diagnosis to Treatment

Gina Bartes, MSc, PhD | Presenter
11:15 AM - 11:30 AM
Convention Center - Mile High Ballroom 4DEF

Patient Perspective: Diagnostic Journey and Disease Impact on Daily Life

Sophie Hansen, BS | Presenter
11:30 AM - 11:45 AM
Convention Center - Mile High Ballroom 4DEF

Patient Perspective: Psychological Aspects of Early Intervention and My Patient Journey

Catarra Simmons | Presenter
11:45 AM - 11:55 AM
Convention Center - Mile High Ballroom 4DEF

Care Coordination, Symptom Management, and Patient Education

Ann Moore, FNP-C | Presenter
11:00 AM - 11:05 AM
Convention Center - Mile High Ballroom 4DEF

Setting the Stage: Introduction and Welcome to Overview of the Unmet Needs in Cholestatic Liver Disease

Bruce Luxon, MD, PhD, FAASLD | Presenter
11:55 AM - 12:25 PM
Convention Center - Mile High Ballroom 4DEF

Panel Discussion

Gina Bartes, MSc, PhD | Moderator

Objectives

  • Outline clinical challenges and evolving standards of care for cholestatic liver disease.
  • Identify key clinical and psychosocial challenges faced by patients with cholestatic liver diseases across the lifespan, particularly with primary sclerosing cholangitis (PSC).
  • Recognize opportunities to incorporate patient advocacy perspectives into clinical practice, research design, and health policy.