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Pathology · Haemodynamics: antithrombin deficiency
Sample itemA 30-year-old woman with extensive iliofemoral thrombosis has an aPTT that barely rises despite escalating intravenous unfractionated heparin doses. Her father also had recurrent thromboses. Which deficiency best explains the heparin resistance?
Original practice item, not a recalled exam question. Nothing here is recorded.
The answer and the reasoning
A. Antithrombin
Heparin acts by binding antithrombin and greatly enhancing its inhibition of thrombin and factor Xa. When antithrombin is inherited at low levels, heparin has little to potentiate, so the aPTT does not prolong and thrombosis recurs. Treatment may need antithrombin replacement or direct inhibitors.
Option by option
A. Antithrombin (correct)
Correct. Heparin needs antithrombin to work, so low levels cause resistance.
B. Protein S
Protein S deficiency causes thrombophilia but does not affect heparin response.
C. Factor XII
Factor XII deficiency prolongs aPTT without bleeding and is not a heparin target.
D. Plasminogen
Plasminogen deficiency impairs fibrinolysis and gives ligneous conjunctivitis, not heparin resistance.
Source note: Original NextPrep sample item — pending expert review. This item is original practice material awaiting independent expert review, so confirm important facts in a standard textbook.
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