How do you diagnose postpartum preeclampsia?

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Last updated: July 8, 2025View editorial policy

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Diagnosing Postpartum Preeclampsia

Postpartum preeclampsia should be diagnosed in women with new-onset hypertension occurring between 48 hours to 6 weeks after delivery, accompanied by at least one feature of end-organ dysfunction, after excluding other etiologies. 1

Definition and Timing

Postpartum preeclampsia is characterized by:

  • New-onset hypertension (≥140/90 mmHg) after delivery
  • Occurs most commonly within the first 7-10 days postpartum 1
  • May develop in women with no prior history of hypertension during pregnancy (55% of cases) 2

Diagnostic Algorithm

Step 1: Blood Pressure Measurement

  • Confirm hypertension: SBP ≥140 mmHg or DBP ≥90 mmHg
  • Classify severity: Mild (140-159/90-109 mmHg) or Severe (≥160/110 mmHg) 3
  • Monitor BP at least every 4 hours while awake for at least 3 days postpartum 3

Step 2: Assess for End-Organ Dysfunction

Look for at least one of the following:

  1. Proteinuria:

    • Screen with automated dipstick urinalysis
    • Confirm with urine protein/creatinine ratio ≥30 mg/mmol (0.3 mg/mg) 3
  2. Neurological symptoms:

    • Headache (most common presenting symptom) 2, 1
    • Visual disturbances/scotomata
    • Hyperreflexia or clonus
    • Altered mental status
    • Seizures (eclampsia)
  3. Laboratory abnormalities:

    • Complete blood count: Thrombocytopenia (<100,000/μL)
    • Liver function tests: Elevated transaminases (AST, ALT)
    • Renal function: Elevated serum creatinine
    • Elevated uric acid 3
  4. Other manifestations:

    • Right upper quadrant/epigastric pain
    • Pulmonary edema
    • HELLP syndrome (Hemolysis, Elevated Liver enzymes, Low Platelets)

Step 3: Exclude Other Causes

Rule out alternative diagnoses such as:

  • Primary seizure disorder
  • Cerebral hemorrhage
  • Drug use
  • Sepsis
  • Thrombotic thrombocytopenic purpura

Diagnostic Workup

  1. Laboratory tests:

    • Complete blood count with platelets
    • Comprehensive metabolic panel (liver enzymes, creatinine, electrolytes)
    • Uric acid level
    • LDH and haptoglobin (if hemolysis suspected)
    • Urinalysis and protein/creatinine ratio 3
  2. Additional tests (based on presentation):

    • Fundoscopy
    • EKG
    • Brain imaging (CT or MRI) if severe headache, visual changes, or neurological symptoms
    • Echocardiography if heart failure or chest pain present 3

High-Risk Populations

Women with higher risk for postpartum preeclampsia include those with:

  • Older maternal age
  • Black race
  • Obesity
  • History of cesarean delivery 1
  • Severe preeclampsia during pregnancy
  • Early-onset preeclampsia during pregnancy 4

Clinical Pearls and Pitfalls

  1. Key pitfall: Assuming women without antepartum preeclampsia cannot develop postpartum preeclampsia. Over half of postpartum preeclampsia cases occur in women with no prior diagnosis during pregnancy 2.

  2. Warning: Headache is the most common prodromal symptom before seizures. All women with postpartum headaches should have their blood pressure checked 2.

  3. Caution: Not all women will present with the "classic" features. Some may have only mild hypertension with other symptoms 2.

  4. Important: Eclamptic seizures may develop for the first time in the early postpartum period, even in women who did not have preeclampsia during pregnancy 3.

  5. Monitoring: Women with preeclampsia should be considered at high risk for complications for at least 3 days postpartum and require close monitoring 3.

By following this systematic approach to diagnosis, postpartum preeclampsia can be identified promptly, allowing for timely intervention to prevent serious maternal complications.

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Research

Analysis of postpartum hypertension in women with preeclampsia.

Journal of human hypertension, 2023

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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