What laboratory tests are recommended for a pregnant woman suspected of having preeclampsia and what is the rationale for each test?

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Laboratory Tests for Preeclampsia

When preeclampsia is suspected, obtain a comprehensive laboratory panel including complete blood count with platelets, liver transaminases, serum creatinine, and urine protein quantification, as these tests directly assess end-organ damage that determines disease severity and guides delivery timing. 1, 2

Essential Initial Laboratory Tests

Proteinuria Assessment

  • Screen with automated dipstick urinalysis; if ≥1+, quantify with spot urine protein/creatinine ratio 1
  • Rationale: Proteinuria ≥30 mg/mmol (0.3 mg/mg) confirms renal involvement and is a diagnostic criterion for preeclampsia, though its absence does not exclude the diagnosis 1, 3
  • A urine albumin-to-creatinine ratio <30 mg/mmol effectively excludes significant proteinuria 1
  • Important caveat: The magnitude of proteinuria does not predict severity or complications and should never be used alone to determine delivery timing 2, 3, 4

Complete Blood Count

  • Hemoglobin and hematocrit to assess for hemoconcentration or hemolysis 1, 2
  • Platelet count is critical—thrombocytopenia <100,000/μL indicates severe features and progressive decline mandates delivery 1, 2, 3
  • Rationale: Platelet consumption reflects endothelial damage and microangiopathic process; progressive thrombocytopenia signals worsening disease requiring immediate delivery regardless of gestational age 1, 2

Liver Function Tests

  • Serum transaminases (AST/ALT) to detect hepatocellular injury 1, 2, 3
  • Lactate dehydrogenase (LDH) for hemolysis assessment 1
  • Rationale: Elevated liver enzymes >2 times upper limit of normal, especially with right upper quadrant or epigastric pain, indicate HELLP syndrome risk and are an indication for delivery 1, 2, 3
  • Liver enzyme elevation correlates with acute clinical deterioration and fetal compromise 5

Renal Function Tests

  • Serum creatinine to assess kidney function—levels ≥1.1 mg/dL or doubling from baseline indicate severe features 2, 3
  • Serum uric acid is associated with worse maternal and fetal outcomes 1, 2
  • Rationale: Progressive elevation in creatinine signals acute kidney injury and is a key indicator for delivery 2
  • Critical pitfall: Uric acid should never be used alone as an indication for delivery 1, 2

Additional Hemolysis Markers (if HELLP suspected)

  • Haptoglobin (decreased in hemolysis) 1
  • Peripheral blood smear for schistocytes 1
  • Rationale: These confirm microangiopathic hemolytic anemia component of HELLP syndrome, which requires immediate treatment and delivery 1

Monitoring Frequency

Perform laboratory testing at minimum twice weekly (every 3-4 days) for all women with diagnosed preeclampsia 1, 2, 3

  • Initial complete panel at diagnosis establishes baseline values 2
  • Repeat hemoglobin, platelets, liver enzymes, and creatinine twice weekly if stable 1, 2
  • Increase to daily or every 48 hours with clinical deterioration, severe features, or any change in maternal condition 2, 3
  • Common pitfall: Inadequate monitoring frequency may miss rapid disease progression—preeclampsia can deteriorate within hours 2, 3

Laboratory-Based Indications for Immediate Delivery

Deliver immediately if any of the following occur, regardless of gestational age 1, 2:

  • Progressive thrombocytopenia (declining platelet count) 1, 2
  • Progressively abnormal liver enzymes 1, 2
  • Worsening renal function (rising creatinine) 1, 2
  • Severe hypertension ≥160/110 mmHg unresponsive to three antihypertensive agents 1, 2

Specialized Testing (Not Routine)

Angiogenic Markers

  • sFlt-1/PlGF ratio can rule out preeclampsia when <38 in clinically suspected cases 1
  • Rationale: Low ratio has strong negative predictive value for short-term absence of preeclampsia 1
  • Current recommendation: Not for routine clinical use; should remain within clinical trials 1, 6

Coagulation Studies

  • Fibrinogen if DIC suspected or severe HELLP syndrome 1
  • Rationale: Assesses for consumptive coagulopathy in severe cases 1

Critical Clinical Pitfalls to Avoid

  • Never classify preeclampsia as "mild" versus "severe" clinically—all cases can rapidly become emergencies 1, 2
  • Do not use proteinuria levels or uric acid alone to determine delivery timing—these do not predict outcomes 1, 2, 3
  • Do not wait for proteinuria to diagnose preeclampsia—approximately 25% of cases lack proteinuria but have other organ dysfunction 3
  • Do not dismiss symptoms without severe blood pressure elevation—34% of eclamptic women had diastolic BP ≤100 mmHg 3
  • Edema is not diagnostic or predictive—should not be used for diagnosis or severity assessment 3

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Guideline

Preeclampsia Diagnosis and Management

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Guideline

Diagnosis and Management of Preeclampsia

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Research

Major changes in diagnosis and management of preeclampsia.

Journal of midwifery & women's health, 2014

Research

Advances in preeclampsia testing.

Advances in clinical chemistry, 2023

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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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