What are the diagnostic criteria for Hellp (Hemolysis, Elevated Liver enzymes, and Low Platelet count) syndrome?

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HELLP Syndrome Diagnostic Criteria

HELLP syndrome is diagnosed by the presence of three components: hemolysis (evidenced by schistocytes on peripheral smear, elevated LDH, or low haptoglobin), elevated liver enzymes (AST/ALT), and thrombocytopenia with platelet count below 100,000/mm³. 1, 2

Core Diagnostic Components

Hemolysis

  • Microangiopathic hemolytic anemia must be confirmed by peripheral blood smear showing schistocytes (fragmented red blood cells) resulting from endothelial damage with fibrin deposition 3
  • Elevated LDH serves as a dual marker reflecting both hemolysis extent and hepatic dysfunction 1, 3
  • Additional supportive findings include elevated indirect bilirubin or low serum haptoglobin levels 2

Elevated Liver Enzymes

  • AST, ALT, LDH, and total bilirubin are the most useful markers for following disease progression and correlate with adverse maternal outcomes 1
  • Significant elevation in liver enzymes must be present, though specific thresholds vary by classification system 2

Low Platelet Count

  • Platelet count below 100,000/mm³ is the threshold established by ACOG for diagnosis and indicates severe thrombocytopenia with significant maternal risk 1, 2
  • The degree of thrombocytopenia directly correlates with severity of liver dysfunction and predicts adverse maternal outcomes 4, 1, 3
  • Platelet count serves as one of the two most important clinical tools for disease assessment alongside LDH 3, 5

Clinical Context and Timing

  • HELLP syndrome typically develops in the third trimester in patients with severe preeclampsia, though approximately 30% of cases occur or worsen postpartum (within 48-72 hours after delivery) 1, 6, 7
  • The syndrome can occur in the absence of classic preeclampsia or eclampsia features, making diagnosis challenging 5, 6
  • Laboratory abnormalities peak 24 hours after delivery and may take up to 10 days to fully resolve 3

Associated Severe Features Requiring Urgent Intervention

When HELLP syndrome is present, look for these additional severe manifestations that mandate immediate delivery 4:

  • Blood pressure exceeding 160/90 mmHg
  • Proteinuria >5 g/24 hours
  • Oliguria <400 mL/24 hours
  • Cerebral signs or symptoms
  • Pulmonary edema
  • Right upper quadrant or epigastric pain (present in 65% of symptomatic patients) - this should immediately trigger imaging to rule out subcapsular hematoma or hepatic rupture 1

Critical Diagnostic Pitfalls

  • Do not wait for all three components to be severely abnormal - partial HELLP syndrome exists and still carries significant risk 2, 7
  • Do not confuse with other conditions including acute fatty liver of pregnancy, idiopathic thrombocytopenia, hemolytic uremic syndrome, or appendicitis 6
  • Obtain abdominal imaging (ultrasound or CT) when hepatic involvement is suspected to rule out hepatic hemorrhage, infarct, or rupture 1

Essential Preoperative Laboratory Workup

Before any surgical intervention, obtain 4:

  • Platelet count, white blood cell count, PCV
  • Partial thromboplastin time, fibrinogen, fibrin degradation products
  • Peripheral blood smear
  • Liver function tests (AST, ALT, LDH, bilirubin)
  • Serum creatinine, urea, and uric acid
  • Chest X-ray to exclude pulmonary edema
  • ECG examination

References

Guideline

Management of HELLP Syndrome

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Guideline

Pathogenesis and Clinical Implications of HELLP Syndrome

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Research

HELLP syndrome--a pregnancy disorder with poor prognosis.

Nepal Medical College journal : NMCJ, 2008

Research

The HELLP syndrome.

Acta clinica Belgica, 2010

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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