Haem Flashcards
Autoimmune haemolytic anaemia
Steroid- prednisolone 1mg/kg of prednisolone daily
Folic acid
B than major
Regular transfusion programme to maintain Hb 95-105
Iron overload
250mg of iron per unit of red cells
Chronic anaemia drives increased iron absorption
NOT VENESECTION (already anaemic)
Iron chelation e.g. desferrioxamine
Sickle crisis
Opiate analgesia
Hydration, rest, oxygen
Antibiotics (if infection)
Red cell exchange transfusion is severe
Long term management of sickling disorder
Hyposplenism- prophylactic penicillin, vaccination
Folic acid supplements
Hydroxycarbamide (increased HbF production)
Haemophilia
Infusions of missing factor
The infusions last for 2 days (major complication of the infusion is the formation of autoantibodies)
Hypersensitivity reaction
Lie patient flat Administer adrenaline Administer chlorampheniramine Administer salbutamol Adminsiter corticosteroids
Incompatible blood type
Exclude major transfusion reaction
Ensure the patients details matched the blood being transfused
Slow the transfusion
Give paracetamol
Instruct nurses to watch the patient closely
Fluid overload
Furosemide to encourage a diuresis and reduce hydrostatic pressure
Venous thrombosis
Heparin/Warfarin/NOACs (anticoagulation)
Arterial thrombosis
Aspirin and other antiplatelets
Modify RF for atherosclerosis
Hereditary thrombolphilias
Avoid risk
Short term prophylaxis
Short term anticoagulant- to prevent thrombotic effect
Long term anticoagulation
Antiphospholipid antibody syndrome
Aspirin and Warfarin
HUS
Dialysis for AKI
Plasma exchange for severe persistent cases
ITP
Prednisolone mainstay
Acute leukaemia
Multi-agent chemotherapy
Pancytopenia
Treat neutropenic fever promptly without waiting for microbiology results
Primary- Chemotherapy, bone marrow transplant or immunosuppression depending on cause
Secondary- Stop drugs, treat virus, replace b12/folate or red cell transfusion
Consider splenectomy
Myeloma
Combination chemotherapy (high dose corticosteroids + alkylating agents)
High dose chemo/autologous stem cell transplant
If cast nephropathy then hydration and stop neophrotoxic drugs
Relapse in inevitable
AL amyloidosis
Chemo
Waldenstroms macroglobinaemia (IgM paraprotein)
Chemotherapy
Plasmapheresis
Chronic myeloid leukaemia
Imatinab
Polycythaemia rubra vera
Take out all of patient blood–> Get the HCT level down to 0.45–> Put it all back in
Give aspirin
Give cytotoxic oral chemo e.g. hydroxycarbomide
Essential thrombocytopenia
Aspirin
Cytoreduction therapy to control proliferation –> hydroxycarbamide, anagrelide, INF alpha
Myelofibrosis
Supportive care- blood transfusion, antibiotics, platelets
Allogenic stem cells transplantation in selected patients (curative but high mortality)
Splenectomy
JAK2 inhibits