In heparin-induced thrombocytopenia (HIT type II), thrombocytopenia occurs due to:
- A Direct toxic effect of heparin on megakaryocytes reducing platelet production
- B IgG antibodies against heparin-platelet factor 4 (PF4) complexes activating platelets via FcγRIIA receptors ✓
- C Complement-mediated lysis of platelets coated with heparin-antibody complexes
- D Consumption of platelets in microthrombi due to von Willebrand factor-rich thrombi
Explanation
HIT type II is an immune-mediated disorder: heparin binds platelet factor 4 (PF4) released from platelets, and this complex is recognized by IgG antibodies. The IgG-PF4-heparin complexes bind FcγRIIA receptors on platelets, causing platelet activation, aggregation, and thrombocytopenia, paradoxically associated with thrombosis (not just bleeding). Treatment requires stopping heparin and substituting a direct thrombin inhibitor (argatroban) or fondaparinux.
Reference: Robbins & Cotran Pathologic Basis of Disease, 10th ed.
High-yield for: NEET PGINI-CETNExTFMGEUSMLEPLABMRCP
Written and medically reviewed by the StethoPrep medical team.