[W7] Bleeding disorders Flashcards
(27 cards)
What are primary haemostatic disorders?
Disorders affecting platelets (number/function).
What is a secondary haemostatic disorder?
Disorders affecting the coagulation cascade.
What is thrombocytopenia?
Platelet count <150×10⁹/L.
Name immune and non-immune causes of thrombocytopenia.
- Immune: ITP
- Non-immune: TTP, DIC
What antibody is found in ITP?
Anti-αIIbβ3.
What is first-line treatment for chronic ITP?
- Corticosteroids
- IVIG
- Splenectomy
What enzyme is deficient in TTP?
ADAMTS13.
What is the classic blood film finding in TTP?
Schistocytes (fragmented RBCs).
What lab features indicate DIC?
- ↓ platelets
- ↑ D-dimer
- Prolonged PT/aPTT
Name 2 DIC triggers.
- Sepsis
- Malignancy
What is the most common inherited platelet disorder?
von Willebrand Disease (VWD).
What test is abnormal in VWD?
Platelet aggregation to ristocetin.
What causes Glanzmann’s thrombasthenia?
GPIIb/IIIa defect → no fibrinogen binding.
How does aspirin affect platelets?
Irreversibly inhibits cyclooxygenase (COX-1).
Why does renal failure cause bleeding?
Uraemia impairs platelet-vessel wall interaction.
What factor is deficient in Haemophilia A?
Factor VIII.
How is Haemophilia A inherited?
X-linked recessive.
What is the treatment for mild Haemophilia A?
- DDAVP
- FVIII concentrate
What disorder is common in Ashkenazi Jews?
Factor XI deficiency.
What vitamin is essential for coagulation?
Vitamin K.
What drug inhibits Vitamin K recycling?
Warfarin.
What causes acquired haemophilia?
Autoantibody against FVIII.
↓ Platelets + Normal PT/aPTT + large platelets = ?
ITP (Immune thrombocytopenia)
Immune thrombocytopenia is a condition characterized by a low platelet count due to immune-mediated destruction.