Flashcards in Bleeding Disorders Deck (13)
What is Von Willebrand Disease (vWF)?
A genetic disorder characterised by missing or defective vWF.
What is the function of von Willebrand Factor (vWF)?
vWF is a protein that promotes platelet aggregation to vascular walls and subsequent clot formation.
It also plays a role in the transport of Factor VIII and in preventing its premature destruction
Describe the defect in each of the three types of vWD
Type I: Reduced levels of normal vWF
Type II: Production of defective vWF
Type III: A total lack of vWF, and a reduced level of Factor VIII.
Which of the three types of vWD are of autosomal dominant and autosomal recessive inheritance?
Type I and II are AD.
Type III is AR.
What treatment options are available for vWD?
Anti-fibrinolytic drugs - Tranexamic acid - given to reduce bleeding.
DDAVP (Desmopressin) - a synthetic vasopressin analogue. DDAVP helps release vWF and Factor VIII from stores. Not useful in Type II and III vWD.
For vWD Type II and III, give Factor VIII concentrate, FFP and cryoprecipitate if severe.
What is TTP?
Thrombotic Thrombocytopenic Purpura
What is the pathophysiology in TTP?
ADAMTS-13 deficiency, leading to increase vWF.
There is also thrombocytopenia and increased bleeding time.
What are the 5 characteristic features of TTP?
4. Neurological symptoms
5. Renal dysfunction
What clotting factors are Vitamin K dependent clotting factors?
Clotting factors II, VII, IX and X.
Which clotting factors are in the intrinsic pathway?
Clotting factors VIII, IX, XI and XII
Describe the pathophysiology of Haemophilia A and B.
Haemophilia A: Deficiency of Factor VIII
Haemophilia B: Deficiency of Factor IX
What are the diagnostic features of DIC?
Low platelet count
Prolonged PT and APTT