Inherited Bleeding Disorders

Key considerations

The lecture duration is 21min.

0.5 CPD Points, 0.5 CEUs, 0.5 CME credits approval pending.
Accredited by CPDUK, CBRN and Provider Pending.

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Thomas DeLoughery
Healthcare Professional at Divisions of Hematology/Oncology and Laboratory Medicine, Oregon Health & Science University, Portland, Oregon, USA
Lecture Summary

This talk goes over the most common causes of inhirted bleeding disorders. There are two major types of hemophilia – deficiency in factor VIII and IX – which predominant occur in men. Hemophilia A is deficiency of factor VIII and is the most common form of hemophilia treated with factor concentrate. Hemophilia B is less common but treatment principles are the same. There are multiple types of von Willebrand Disease as this is a complex molecular that both carries factor VIII and forms large multimers essential for platelet function. Mild forms of vWD can be treated by desmopressin but von Willebrand factor is needed for more severe types.

Target Audience

Emergency Medicine Doctors
Emergency Medicine Nurses
Paramedics
Rural GP's

Learning Objectives:

Upon completion of this activity, you should be able to:

  • Understand the patterns of bleeding in hemophilia
  • Learn how to dose clotting factor for hemophilia
  • Understand the different types of von Willebrand Diseases and their treatments