4.00
(1 Rating)

AL Amyloidosis: Identifying Patients, Implementing Care

Wishlist Share
Share Course
Page Link
Share On Social Media

About Course

Program Description

Light chain (AL) amyloidosis, a rare clonal plasma cell disorder characterized by organ deposition of amyloid protein, results in progressive organ damage that is usually irreversible. Prompt treatment is critical to achieving the best possible outcomes, but rapid initiation of treatment requires early, accurate diagnosis, which is often delayed because of the nonspecific nature of the symptoms. Unfortunately, delayed diagnosis is a grave concern, as the median survival rate among some untreated patients is approximately 6 months following symptom onset.

A high index of suspicion and appropriate testing are needed to make a diagnosis of AL amyloidosis, but the significant delays and multiple physician visits patients typically encounter (many patients report seeing at least five physicians, including cardiologists and nephrologists, before receiving a diagnosis) indicate that clinicians continue to be confounded by this condition’s highly variable clinical presentation.

Therapies for AL amyloidosis target the aberrant plasma/B-cell clone and have traditionally been based on regimens adapted from the expanding treatment options available for multiple myeloma; however, in January 2021 the FDA approved a therapy specifically for use in patients with AL amyloidosis.

This activity features a roundtable discussion with a multidisciplinary panel of experts on the latest information on evidence-based diagnosis and treatment guidelines for patients with AL amyloidosis.

Educational Objectives

Upon completion, participants should be able to:

  • Recognize the clinical presentations that should raise suspicion of AL amyloidosis
  • Utilize optimal diagnostic testing to minimize delays in treatment initiation
  • Outline current and emerging treatment options that are available to treat patients with AL amyloidosis, using supporting clinical trial data

Intended Audience

This activity is designed to meet the educational needs of hematologist-oncologists, medical oncologists, oncology nurses, cardiologists, nephrologists, and other health care providers involved in the diagnosis and treatment of patients with AL amyloidosis.

Commercial Supporter

This activity is supported by educational grants from The Binding Site and Janssen Biotech Inc., administered by Janssen Scientific Affairs, LLC.

Max Credits

  • 1.00 / AMA PRA Category 1 Credit(s)
  • 1.00 / ABIM MOC Part II Points
  • 1.00 / CNE Contact Hour(s)

Expires: June 6, 2023

Show More

What Will You Learn?

  • Become a UX designer.
  • You will be able to start earning money from your XD Skills.
  • You will be able to add UX designer to your CV
  • Build a UX project from beginning to end.
  • Become a UI designer.
  • Build & test a full mobile app.

Student Ratings & Reviews

4.0
Total 1 Rating
5
0 Rating
4
1 Rating
3
0 Rating
2
0 Rating
1
0 Rating
6 years ago
Just completed the course:) Thank you so much, it was easy to follow and a big step, onwards and upwards, I also got your course on dreamweaver and I'm looking forward to getting stuck in. I'm sure will be as helpful and laid back as the last, really happy thank you.