What is the emergency management for a pregnant woman at ≥20 weeks gestation presenting with preeclampsia?

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Emergency Management of Preeclampsia

Women presenting with preeclampsia at ≥20 weeks gestation require immediate assessment for severe features, urgent blood pressure control if BP ≥160/110 mmHg, magnesium sulfate for seizure prophylaxis when severe features are present, and delivery planning based on gestational age and disease severity. 1

Immediate Stabilization and Assessment

Blood Pressure Management

  • Initiate urgent antihypertensive therapy immediately when BP ≥160/110 mmHg persists for >15 minutes to prevent maternal cerebral hemorrhage. 1, 2
  • First-line IV options include:
    • IV labetalol: 20 mg IV bolus, then 40 mg after 10 minutes, then 80 mg every 10 minutes (maximum cumulative dose 220 mg) 1
    • IV hydralazine: 5-10 mg IV every 20 minutes as needed 1
    • Oral nifedipine is preferred for urgent BP control when IV access is not immediately available 2
  • Target BP: systolic 110-140 mmHg and diastolic 85 mmHg (or at minimum <160/105 mmHg). 1, 2, 3
  • For non-severe hypertension (BP 140-159/90-109 mmHg), use oral agents: methyldopa, labetalol, or nifedipine 1

Seizure Prophylaxis with Magnesium Sulfate

  • Administer magnesium sulfate immediately to all patients with severe preeclampsia, proteinuria plus severe hypertension, or any neurological symptoms (headache, visual changes). 1, 2, 3
  • Loading dose: 4-5 g IV over 5 minutes (diluted in 250 mL of 5% dextrose or 0.9% normal saline) 1
  • Maintenance: 1-2 g/hour continuous IV infusion 1
  • Continue for 24 hours postpartum, as eclampsia can occur in the postpartum period 2

Identify Severe Features Requiring Urgent Intervention

Severe features include any of the following: 1, 2

  • Severe hypertension: BP ≥160/110 mmHg on two occasions at least 15 minutes apart
  • Thrombocytopenia: platelets <100,000/μL
  • Renal dysfunction: creatinine >1.1 mg/dL or doubling of baseline
  • Liver involvement: elevated transaminases (AST/ALT ≥2x upper limit of normal) 1
  • Neurological symptoms: severe headache, visual disturbances (scotomata, cortical blindness), altered mental status
  • Pulmonary edema 1, 2
  • Epigastric or right upper quadrant pain (hallmark of HELLP syndrome) 1, 2

Comprehensive Laboratory Assessment

Obtain immediately: 1, 2, 3

  • Complete blood count with focus on hemoglobin and platelet count
  • Comprehensive metabolic panel: liver transaminases (AST/ALT), creatinine, uric acid
  • Spot urine protein/creatinine ratio (≥30 mg/mmol confirms proteinuria, though proteinuria is no longer mandatory for diagnosis) 1

Fetal Assessment

  • Continuous electronic fetal heart rate monitoring to assess for non-reassuring fetal status 2, 3
  • Biophysical profile including ultrasound assessment of fetal biometry, amniotic fluid volume, fetal breathing movements, body movements, and tone 3
  • Non-reassuring fetal status is an absolute indication for immediate delivery regardless of gestational age 1, 2

Delivery Timing: Gestational Age-Based Algorithm

At ≥37 Weeks Gestation

  • Deliver immediately after maternal stabilization regardless of severity or laboratory values. 1, 3
  • Do not delay delivery based on non-reactive NST—delivery is indicated regardless of fetal testing results 3

At 34-37 Weeks Gestation

  • Without severe features: expectant management with close monitoring is appropriate 1
  • With severe features: deliver after maternal stabilization 1, 3

At <34 Weeks Gestation

  • Expectant management is possible in select cases under intensive monitoring 4, 5
  • Administer corticosteroids for fetal lung maturity between 24-34 weeks 4

Absolute Indications for Immediate Delivery (Any Gestational Age)

Deliver immediately regardless of gestational age if: 1, 2

  • Inability to control BP despite ≥3 classes of antihypertensives in appropriate doses
  • Eclamptic seizures (after maternal stabilization with magnesium sulfate)
  • Progressive thrombocytopenia (declining platelet counts on serial measurements) 1
  • Progressively abnormal liver or renal function tests (worsening trends, not static elevations) 1
  • Placental abruption
  • Non-reassuring fetal status on continuous monitoring
  • Pulmonary edema
  • Maternal oxygen saturation deterioration (<90%)

Special Considerations for HELLP Syndrome

  • HELLP syndrome is defined by hemolysis, elevated liver enzymes (AST/ALT ≥2x upper limit), and low platelets (<100,000/μL) 1
  • Maternal mortality rate is 3.4% in HELLP syndrome 1, 2
  • Epigastric or right upper quadrant pain is the hallmark symptom 1, 2
  • Monitor glucose intraoperatively as severe hypoglycemia can occur 1
  • HELLP syndrome should be managed as severe preeclampsia with immediate delivery planning 1

Management of Pulmonary Edema

  • Drug of choice is IV nitroglycerin (glycerol trinitrate) starting at 5 mcg/min, gradually increased every 3-5 minutes to maximum 100 mcg/min 1, 6
  • Limit fluid balance to 60-80 mL/hour to avoid worsening pulmonary edema, with target urine output of 0.5-1 mL/kg/hour 2
  • Plasma volume expansion is NOT recommended routinely 1

Monitoring Protocol

Maternal Monitoring

  • Blood pressure: at least every 4 hours while awake, or continuously if severe features present 1, 2
  • Laboratory tests: repeat at least twice weekly (hemoglobin, platelets, liver enzymes, creatinine, uric acid) 1
  • Assess for visual disturbances, epigastric/right upper quadrant pain, headache 2
  • Monitor fluid balance and urine output 2, 6

Setting of Care

  • Women with severe features should be managed in facilities with appropriate obstetrical care, maternal intensive care capabilities, and NICU for premature infants. 1

Critical Pitfalls to Avoid

  • Do not underestimate disease severity based on "mild" classification—all preeclampsia can rapidly progress to life-threatening complications 1, 2, 3
  • Blood pressure alone is not a reliable indicator of disease severity—serious organ dysfunction can develop at relatively mild levels of hypertension 1, 3
  • Do not use serum uric acid or level of proteinuria as indication for delivery 1
  • Do not delay delivery at ≥37 weeks based on non-reactive NST—delivery is indicated regardless of fetal testing results 3
  • Do not reduce antihypertensives if diastolic BP falls <80 mmHg 1
  • Do not use diuretics routinely—they further reduce plasma volume which is already contracted in preeclampsia 1
  • Avoid NSAIDs for postpartum analgesia unless other analgesics are not working, especially if renal disease or placental abruption are present 2

Postpartum Management

  • Continue magnesium sulfate for 24 hours postpartum 2
  • Monitor BP at least every 4-6 hours for at least 3 days postpartum 2
  • Continue neurological monitoring as postpartum eclampsia remains a risk 2
  • Repeat laboratory tests the day after delivery and then every other day until stable 2
  • Review all women at 3 months postpartum to ensure BP, urinalysis, and laboratory abnormalities have normalized 1

References

Guideline

Management of Preeclampsia

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2026

Guideline

Management of Eclampsia

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2026

Guideline

Management of Mild Preeclampsia at 37 Weeks

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Research

[Treatment of severe preeclampsia and HELLP syndrome].

Zentralblatt fur Gynakologie, 2004

Research

Severe pre-eclampsia and hypertensive crises.

Best practice & research. Clinical obstetrics & gynaecology, 2013

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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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