Criteria
Laboratory criteria for HELLP syndrome
The following laboratory criteria should be met for a diagnosis of HELLP syndrome:[1][10][30]
Hemolysis, as evidenced by the presence of schistocytes, burr cells, and polychromasia on a peripheral smear. However, peripheral blood smears are not routinely performed in clinical practice, and sufficient evidence of hemolysis can be gained from:
Elevated LDH (>600 IU/L or twice the upper limit of normal concentration)
Elevated bilirubin (>1.2 mg/dL)
Low serum haptoglobin (rarely performed in practice)
Elevated liver transaminases: aspartate aminotransferase and/or alanine aminotransferase >70 IU/L, or twice the upper limit of normal concentration not accounted for by alternative diagnoses
Thrombocytopenia: platelets <100,000/mm³.
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