Heparin-induced thrombocytopenia differential diagnosis: Difference between revisions
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==Differential diagnosis== | ==Differential diagnosis== | ||
The table below summarizes the different findings between HIT and other diseases in the differential diagnosis | The table below summarizes the different findings between HIT and other diseases in the differential diagnosis. Please scroll down to view the table. | ||
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! scope="col" | Characteristic/Parameter | ! scope="col" | Characteristic/Parameter |
Revision as of 21:45, 29 July 2017
Heparin-induced thrombocytopenia |
Differentiating Heparin-induced thrombocytopenia from other Diseases |
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Diagnosis |
Treatment |
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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] 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 and others.
Differential diagnosis
The table below summarizes the different findings between HIT and other diseases in the differential diagnosis. 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.