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On-Demand Webinar

Exploring Treatment Options in Fabry Disease to Address Management Gaps and Improve Patient Outcomes

Release Date

January 9, 2023

Expiration Date

January 10, 2024

Credits

1.25 On-Demand

Topics

Rare Diseases

Program Description

Fabry disease is a rare, X-linked, lysosomal storage disease caused by a deficiency in the lysosomal enzyme α-galactosidase (α-GAL). α-Gal A is responsible for the breakdown of glycolipids, specifically globotriaosylceramide (GL-3 or Gb3). This enzyme deficiency results in a continuous build-up of GL-3/Gb3 and related glycolipids in the body’s cells, leading to cell abnormalities and organ dysfunction that affects small blood vessels, the heart, and kidneys. Enzyme replacement therapy has been shown to decrease disease complications and slow progression, but its frequent administration and adverse reactions present therapeutic challenges for patients. Pharmacists in specialty practice settings are well positioned to facilitate access to emerging drug therapies and provide support to the multidisciplinary care team by helping navigate treatment selection, monitoring and managing drug-drug interactions, and providing guidance for dose adjustments. This webinar will provide an introduction to Fabry disease with a look at the role of adjunctive and emerging therapies. Educational points for pharmacists to share with patients regarding goals of treatment, adverse effects, and preparation and administration of drug therapies will also be reviewed.


Target audience: Health-system, managed care, retail, and specialty pharmacists

Type of activity: Application
Release date: January 9, 2023
Expiration date: January 9, 2024

Time to complete activity: 1.25 hour
Fee: Free

Educational Objectives

At the completion of this activity, participants will be able to:

  • Investigate the pathophysiology, phenotypes, and clinical manifestations of Fabry disease
  • Explore the efficacy and safety of current and emerging drug therapies for Fabry disease
  • Determine evidence-based strategies for treatment as new data become available
  • Identify methods to overcome treatment challenges in Fabry disease and implement individualized care strategies
Exploring Treatment Options in Fabry Disease to Address Management Gaps and Improve Patient Outcomes

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This activity is supported by educational grants from Chiesi and Intellisphere LLC.

What's Included
  • Access your activities anytime, anywhere, with a computer, tablet or smartphone
  • Free access with a PTCE account
  • Pharmacy education designed to improve patient care

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Exploring Treatment Options in Fabry Disease to Address Management Gaps and Improve Patient Outcomes

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