Critical Advances in the Management of Immune Thrombocytopenic Purpura
Summaries of Lectures From a Satellite Symposium Held in Conjunction With the 50th ASH Annual Meeting and Exposition
San Francisco, CA
December 6-9, 2008
Release Date: May 23, 2009
Expiration Date: May 23, 2010
PER Editorial Staff
Immune thrombocytopenic purpura (ITP) is an autoimmune disease characterized by a low platelet count and mucocutaneous bleeding. The low platelet count seen in patients with ITP is the result of accelerated platelet destruction mediated by antiplatelet antibodies and, in some cases, impaired platelet production. The goal of ITP management is to raise and maintain platelet counts in order to prevent life-threatening bleeding events and to improve patient quality of life. Treatment standards for ITP have not changed substantially in > 10 years. Corticosteroids have long been the standard first-line therapy for adults with ITP. Other initial treatment options include intravenous immunoglobulin and anti-D. Splenectomy remains a viable option for patients with refractory ITP, and the anti-CD20 antibody rituximab also has efficacy in this setting. The development of thrombopoietin receptor agonists (TPO-RAs) has provided a new and effective treatment option for the management of patients with refractory ITP.
The purpose of this activity is to update physicians on the treatment of patients with ITP.
This educational activity is intended for medical oncologists and hematologists involved in the care of patients with ITP. No specific skills or knowledge other than a basic training in oncology is required for successful participation in this activity.
Upon completion of this educational activity, you should be able to:
You will be permitted 2 attempts to successfully complete the Posttest.