Haematology · 5-min blitz

0 / 0
Bleeding Thrombophilia / haemolysis Systemic disease Lymphoma / myeloma / CLL tap a card to reveal
Decoderskeep these in your head — they solve most of the cases

Clotting screen → which pathway

PT / INRExtrinsic + common (VII). Prolonged by warfarin, factor VII, liver disease, vit K deficiency. Monitors warfarin.
APTTIntrinsic + common (VIII, IX, XI, XII). Prolonged by heparin, haemophilia A/B, vWD, lupus anticoagulant. Monitors unfractionated heparin.
TTFibrinogen → fibrin. Prolonged by low/abnormal fibrinogen and heparin.
Mixing 50/50Corrects = factor deficiency  ·  Fails to correct = inhibitor (antibody).
Vit K factorsII, VII, IX, X + protein C & S.

Schistocytes + low platelets (MAHA) → which one

HELLPPregnant, on pre-eclampsia background → deranged LFTs + haemolysis + low platelets.
TTPPentad: MAHA, ↓platelets, fever, renal, neuro. Normal coag screen. ADAMTS13 deficiency → treat with plasma exchange.
HUSMAHA + ↓platelets + acute kidney injury. Child, post E. coli O157 diarrhoea.
DIC↑PT + ↑APTT + ↓fibrinogen + ↑D-dimer. Sepsis, trauma, malignancy, obstetric.
Trap: never give platelet transfusion in TTP unless life-threatening bleed — it fuels thrombosis.

Cytopenia thresholds

Platelets <50spontaneous bleeding risk begins
Platelets <10prophylactic platelet transfusion (no bleeding)
Neutrophils <0.5severe infection risk
Neutrophils <0.1 >5 daysbacterial then fungal infection common