Haem - Thrombocytopenia Flashcards
What is the normal platelet range?
150-450 x10^9
What are the two categories which cause low platelets?
Decreased production
Increased destruction
What can cause reduced platelet production?
- Viral infections e.g. EBV, CMV, HIV
- B12 deficiency
- Folate deficiency
- Liver failure - reduced thrombopoietin production
- Leukaemia
- Myelodysplastic syndrome
- Chemotherapy
What can cause increased platelet destruction?
- Medications e.g sodium valproate and methotrexate
- Alcohol
- Immune thrombocytopenic purpura
- Thrombotic thrombocytopenic purpura
- Heparin-induced thrombocytopenia
- Haemolytic uraemic syndrome
How can thrombocytopenia present?
Usually when platelets under 50x10^9
- Nosebleeds
- Bleeding gums
- Heavy periods
- Easy bruising
- Haematuria
- Rectal bleeding
Platelets below 10x10^9 are at high risk of spontaneous bleeding
- Intracranial haemorrhage
- GI bleeding
What are the most likely differentials for abnormal bleeding?
Thrombocytopenia
Von Willebrand disease
Haemophilia A and B
Disseminated intravascular coagulation (usually secondary to sepsis)
What is immune thrombocytopenic purpura?
Antibodies created against platelets leading to destruction and low platelet count
Characteristically presents with purpura
How is immune thrombocytopenic purpura managed?
Monitoring platelet count, controlling BP and suppressing menstrual periods
- Prednisolone
- IV immunoglobulins
- Thrombopoietin receptor agonists
- Rituximab
- Splenectomy
What is an example of a thrombopoietin receptor agonist?
Avatrombopag
How does Rituximab work?
Targets CD20 proteins on surface of B cells
By attacking B cells and reducing their number, it reduces production of antibodies that are causing autoimmune disease
What is thrombotic thrombocytopenic purpura?
Condition where tiny thrombi develop throughout small vessels using up platelets
Microangiopathy as it effects small vessels
What does thrombotic thrombocytopenic purpura cause?
Thrombocytopenia
Purpura
Tissue ischaemia and end-organ damage
Why do thrombi develop in thrombotic thrombocytopenic purpura?
Issue with ADAMTS13 protein
Normally the protein :
- Inactivates Von Willebrand factor
- Reduced platelet adhesion to vessel walls
- Reduces clot formation
What can cause a deficiency in ADAMTS13 protein?
Inherited
Autoimmune disease, antibodies attack the protein
How is thrombotic thrombocytopenic purpura treated?
Haematologist guided
Plasma exchange
Steroids
Rituximab