Heparin-induced thrombocytopenia differential diagnosis

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Heparin-induced thrombocytopenia

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-In-Chief: Priyamvada Singh, M.B.B.S. [2]

Overview

Heparin-induced thrombocytopenia is diagnosed when the platelet count falls by > 50% typically after 5-10 days of heparin therapy. It should be differentiated by other causes of thrombocytopenia like hemolytic uremic syndrome, Thrombotic thrombocytopenia and others.

Differential diagnosis

Diagnosis of Heparin-induced thrombocytopenia is mainly done with the help of lab tests. A decrease in platelet count by > 50% typically after 5-10 days of heparin therapy leads to a diagnosis of HIT. Thus, it should be differentiated from other causes of thrombocytopenia like

The table below summarizes the different findings between HIT and other diseases in the differential diagnosis:

Characteristic/Parameter HIT DIC HUS ITP PTP SLE
Symptoms Bleeding, thrombosis, skin necrosis. Bleeding, thrombosis, petechiae, sepsis. Renal failure, hematuria, bleeding, microangiopathic hemolytic anemia. Petechiae, bleeding, other autoimmune diseases. Petechiae, purpura, ecchymoses. Bleeding, photosensitivity, arthritis, malar rash, discoid rash, renal failure, seizures, psychosis.
Platelet count Low but usually more than 20000 per microliter. Low. Low. Low; can be as low as 10000 per microliter. Low; can be less than 10000 per microliter; sudden onset after transfusion. Variable; usually low.
PT and PTT Does not change the pain Can increase the pain
Systemic systems Pain is worse supine or upon inspiration (breathing in) Not positional
Drug-related Sudden pain, that lasts for hours or sometimes days before a patient comes to the ER Sudden or chronically worsening pain that can come and go in paroxysms or it can last for hours before the patient decides to come to the ER
Bleeding Does not change the pain Can increase the pain

Table legend: HIT, heparin-induced thrombocytopenia; DIC, disseminated intravascular coagulation; HUS, hemolytic-uremic syndrome; ITP, immune thrombocytopenia purpura; PTP, post-transfusion purpura; SLE, systemic lupus erythematosis

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