Thrombocytopenia Flashcards
Causes of thrombocytopenia
Decreased production
- BM dysfunction
- Drugs
- Megaloblastic anaemia
- Inherited platelet disorders
Increased destruction and consumption
- ITP
- Alloimmune
- Drugs
- HITTs
- DIC
- TTP
- Hypersplenism
- Malaria
- Snake venom
ITP pathogenesis and presentation
Antibody mediated destruction of platelets by the liver and spleen
F»>M
May present with mucocutaneous bleeding
Isolated thrombocytopenia
Associated with AIHA, CLL, SLE and RA, HCV
ITP management
Aim to maintain platelets >30
Prednisone
IVIG
Splenectomy
Romiplostim - TPO receptor agonist
Eltrombopeg - TPO mimetic
Immunosuppression
DIC pathogenesis
Thrombocytopenia and abnormal coagulation profile
- Increased PT and ApTT
- Reduced fibrinogen
- High D-dimer
Fibrin deposition
Microvascular dysfunction
Consumption of platelets and coagulation proteins with increased bleeding risk
DIC management
Identify and manage underlying cause
Bleeding:
- Platelet transfusion
- FFP
- Cyroprecipitate
HITTS Pathogenesis
Caused by formation of IgG antibody that recognises heparin-PF4 complexes
Heparin-PF4 complexes bind to platelet surfaces –> platelet activation and consumption
PROTHROMBOTIC STATE
Develops 5-14 days after exposure to heparin
Platelets fall by >50% rarely <15
High risk of thrombosis
HITTS diagnosis and management
HIT pretest probability
Immunoassay to detect HIT antibody that binds PF4
Functional assay - serotonin release assay or heparin induced platelet aggregation
Cease heparin
Direct thrombin inhibitor or Xa inhibitor
Avoid warfarin
Thrombocytopenia in pregnancy
Gestational thrombocytopenia - platelets >80
ITP in pregnancy
HELLP