What is the hemolysis cutoff for diagnosing HELLP (Hemolysis, Elevated Liver enzymes, and Low Platelet count) syndrome according to William's 26th edition?

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Last updated: June 26, 2025View editorial policy

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From the Guidelines

According to the provided evidence, the hemolysis cutoff for diagnosing HELLP syndrome is not explicitly stated in terms of a specific numerical value for lactate dehydrogenase (LDH) level or other markers of hemolysis in the context of William's 26th edition. However, the diagnosis of HELLP syndrome involves evidence of microangiopathic hemolytic anemia, which can be indicated by an abnormal peripheral blood smear showing schistocytes, and elevated liver enzymes, along with low platelet count. The elevated LDH level, as mentioned in some studies, reflects tissue damage and hemolysis but a specific cutoff value is not provided in the given references. Key points to consider in the diagnosis and management of HELLP syndrome include:

  • Evidence of microangiopathic hemolytic anemia
  • Elevated liver enzymes (such as AST or ALT)
  • Low platelet count
  • Prompt diagnosis and management are crucial, typically involving delivery of the fetus and supportive care. Given the severity of HELLP syndrome and its potential for significant morbidity and mortality, clinicians should prioritize prompt recognition and management based on clinical presentation and laboratory findings, even in the absence of a specific hemolysis cutoff value 1.

From the Research

Hemolysis Cutoff for HELLP Syndrome

According to the provided studies, the hemolysis cutoff for diagnosing HELLP syndrome is not explicitly stated in the context of William's 26th edition. However, the studies provide some insights into the laboratory criteria for diagnosing HELLP syndrome:

  • A study published in 1998 2 mentions that the most reliable laboratory tests for the diagnosis of HELLP are a complete blood count with peripheral smear, lactate dehydrogenase, serum transaminases, and urinalysis.
  • Another study published in 2016 3 found that lactate dehydrogenase ≥ 600 U/L was a useful biomarker for hemolysis in patients with HELLP syndrome.
  • A study published in 2004 4 states that the diagnosis of HELLP syndrome requires the presence of hemolysis based on examination of the peripheral smear, elevated indirect bilirubin levels, or low serum haptoglobin levels in association with significant elevation in liver enzymes and a platelet count below 100,000/mm(3).
  • A study published in 2007 5 found that the level of total bilirubin (indicating the degree of hemolysis) was a useful indicator of the progression of HELLP syndrome.

Key Laboratory Criteria

Some key laboratory criteria for diagnosing HELLP syndrome include:

  • Lactate dehydrogenase ≥ 600 U/L 3
  • Elevated indirect bilirubin levels 4
  • Low serum haptoglobin levels 4
  • Platelet count below 100,000/mm(3) 4
  • Total bilirubin levels (indicating the degree of hemolysis) 5

William's 26th Edition

Unfortunately, there is no direct reference to William's 26th edition in the provided studies, and therefore, it is not possible to determine the hemolysis cutoff for HELLP syndrome according to this specific edition.

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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