Heparin-induced thrombocytopenia differential diagnosis
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-In-Chief: Priyamvada Singh, M.B.B.S. [2] Shyam Patel [3]
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, disseminated intravascular coagulation, post-transfusion purpura, and systemic lupus erythematosis.
Differential diagnosis
HIT must be differentiated from other diseases that present with thrombocytopenia. Please scroll down to view the table.
Characteristic/Parameter | HIT | DIC | HUS[1] | Atypical HUS | ITP | PTP | SLE |
---|---|---|---|---|---|---|---|
Symptoms | Bleeding, thrombosis, skin necrosis | Bleeding, thrombosis, petechiae, sepsis | Renal failure, hematuria, bleeding, microangiopathic hemolytic anemia | 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 | 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 | Normal | Elevated | Normal | Normal | Normal | Normal | Usually normal |
Etiology | Heparin exposure | Sepsis, delivery of fetus, acute promyelocytic leukemia, other malignancy | E.coli strain O157:H7; Shiga-like toxin | Dysregulation of complement activation; mutation in complement factor H | Idiopathic; can be secondary to chronic lymphocytic leukemia, HIV, viral hepatitis, H. pylori | Exposure to transfused products | Autoimmunity with development of antibodies to DNA |
Drug-related | Yes, always | Possible | No | No | Yes | No; transfusion-related | Possible; drug-induced lupus can be caused by medications like hydralazine or isoniazid |
Bleeding | Possible | Usually | Usually | Usually | Yes; spontaneous bleeding if platelet count < 10000 per microliter | Yes; spontaneous bleeding if platelet count < 10000 per microliter | Rare |
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
Reference
- ↑ Jokiranta TS (2017). "HUS and atypical HUS". Blood. 129 (21): 2847–2856. doi:10.1182/blood-2016-11-709865. PMC 5445567. PMID 28416508.