What is the management of preeclampsia?

Medical Advisory BoardAll articles are reviewed for accuracy by our Medical Advisory Board
Educational purpose only • Exercise caution as content is pending human review
Article Review Status
Submitted
Under Review
Approved

Last updated: December 17, 2025View editorial policy

Personalize

Help us tailor your experience

Which best describes you? Your choice helps us use language that's most understandable for you.

Management of Preeclampsia

Delivery is the only definitive treatment for preeclampsia, but the timing depends on gestational age, disease severity, and maternal-fetal status—with immediate delivery indicated for severe features at ≥34 weeks or any gestational age if maternal or fetal deterioration occurs. 1, 2

Initial Assessment and Hospitalization

  • All women with newly diagnosed preeclampsia require initial hospitalization to confirm diagnosis, assess severity, and establish monitoring protocols 1
  • Preeclampsia is diagnosed by new-onset hypertension (≥140/90 mmHg) after 20 weeks of gestation with either proteinuria (≥300 mg/24h or spot protein/creatinine ratio ≥30 mg/mmol) or evidence of end-organ damage 1, 3
  • Proteinuria is no longer required for diagnosis if other features of end-organ dysfunction are present (thrombocytopenia, renal insufficiency, liver involvement, neurological symptoms, or fetal growth restriction) 3

Blood Pressure Management

Severe Hypertension (≥160/110 mmHg)

Severe hypertension requires urgent treatment within 15 minutes in a monitored setting to prevent maternal cerebral hemorrhage while maintaining uteroplacental perfusion. 1, 2

First-line IV antihypertensive options: 1, 2

  • Labetalol: 20 mg IV bolus, then 40 mg after 10 minutes, followed by 80 mg every 10 minutes to maximum 220 mg
  • Nifedipine (oral): 10 mg, repeat every 20 minutes to maximum 30 mg
  • Nicardipine (IV): Start at 5 mg/h, increase by 2.5 mg/h every 5-15 minutes to maximum 15 mg/h

Target blood pressure: Systolic 110-140 mmHg and diastolic 85 mmHg (or at minimum <160/105 mmHg) 1, 2

Non-Severe Hypertension (140-159/90-109 mmHg)

  • Treat with oral antihypertensives targeting diastolic BP of 85 mmHg and systolic BP between 110-140 mmHg 1
  • Acceptable oral agents include methyldopa, labetalol, and long-acting nifedipine 4

Critical Contraindications

  • ACE inhibitors and ARBs are absolutely contraindicated during second and third trimesters due to fetal renal dysgenesis 5, 2
  • Avoid sublingual nifedipine due to risk of precipitous blood pressure drops causing maternal myocardial infarction or fetal distress 1
  • Sodium nitroprusside should only be used as last resort in extreme emergencies due to risk of fetal cyanide poisoning 2
  • Do not combine IV magnesium sulfate with calcium channel blockers due to risk of severe hypotension and myocardial depression 1, 4

Magnesium Sulfate for Seizure Prophylaxis

Magnesium sulfate must be administered for seizure prophylaxis in all women with severe preeclampsia or those with neurological symptoms. 1, 2, 6

Dosing Regimens 6

IV Regimen (preferred when infusion pumps available):

  • Loading dose: 4-5 g IV over 5 minutes (diluted in 250 mL of 5% dextrose or 0.9% saline)
  • Maintenance: 1-2 g/hour continuous IV infusion

Combined IV/IM Regimen (Pritchard):

  • Loading dose: 4 g IV over 3-4 minutes PLUS 10 g IM (5 g in each buttock) for total of 14 g
  • Maintenance: 5 g IM into alternate buttocks every 4 hours

Duration: Continue for 24 hours after delivery or last seizure, whichever is later 4, 6

Monitoring for Magnesium Toxicity 1, 2, 6

  • Assess deep tendon reflexes (patellar) before each dose—loss indicates toxicity
  • Monitor respiratory rate continuously—respiratory depression occurs at toxic levels
  • Maintain urine output ≥100 mL over 4 hours (or >35 mL/hour via Foley catheter)
  • Therapeutic serum magnesium level: 4-7 mEq/L (optimal for seizure control: 6 mg/100 mL) 6
  • Have injectable calcium gluconate or calcium chloride immediately available to reverse toxicity 4

Critical Warnings 6

  • Do not administer magnesium sulfate continuously beyond 5-7 days as it causes fetal skeletal demineralization, osteopenia, and neonatal fractures
  • Maximum total daily dose: 30-40 g in 24 hours 6
  • In severe renal insufficiency, maximum dose is 20 g/48 hours with frequent serum level monitoring 6

Fluid Management

Strictly limit total fluid intake to 60-80 mL/hour to prevent pulmonary edema. 1, 2, 4

  • Replace insensible losses (30 mL/hour) plus anticipated urinary output (0.5-1 mL/kg/hour) 4
  • Preeclamptic women have capillary leak and reduced plasma volume, making them highly susceptible to pulmonary edema with excessive fluids 4
  • Diuretics are contraindicated as plasma volume is already reduced 1, 4
  • Aim for euvolemia; avoid "running dry" as this increases acute kidney injury risk 1

Maternal Monitoring

Clinical Assessment 1, 2

  • Blood pressure every 4 hours (more frequently if severe features present)
  • Hourly urine output via Foley catheter with target ≥100 mL/4 hours
  • Oxygen saturation on room air (maternal early warning if <95%)
  • Assess for severe headache, visual disturbances, epigastric or right upper quadrant pain
  • Monitor for clonus, altered mental status, shortness of breath

Laboratory Monitoring 1, 2

At least twice weekly (more frequently with clinical deterioration):

  • Complete blood count (hemoglobin, platelet count)
  • Liver transaminases (AST, ALT)
  • Serum creatinine and uric acid
  • Peripheral blood smear if HELLP syndrome suspected

Fetal Monitoring

  • Initial ultrasound assessment: fetal biometry, amniotic fluid volume, umbilical artery Doppler 1
  • Repeat ultrasound every 2 weeks if initial assessment normal, more frequently if fetal growth restriction present 1, 2
  • Continuous or intermittent fetal heart rate monitoring depending on severity 2

Timing of Delivery

Delivery Indications by Gestational Age 1, 2

≥37 weeks: Deliver after maternal stabilization with magnesium sulfate and blood pressure control

34-37 weeks:

  • Expectant conservative management appropriate if maternal and fetal status stable
  • Deliver if any maternal or fetal deterioration occurs

<34 weeks:

  • Conservative expectant management at center with Maternal-Fetal Medicine expertise
  • Administer corticosteroids for 48 hours to accelerate fetal lung maturation 5, 1

<24 weeks:

  • Expectant management associated with high maternal morbidity with limited perinatal benefit
  • Counsel regarding pregnancy termination 2

Absolute Indications for Immediate Delivery (Any Gestational Age) 1, 2, 4

  • Inability to control blood pressure despite ≥3 classes of antihypertensives in appropriate doses
  • Progressive thrombocytopenia or HELLP syndrome
  • Progressively abnormal liver or renal function tests
  • Pulmonary edema
  • Severe intractable headache, repeated visual scotomata, or eclamptic seizures
  • Placental abruption
  • Non-reassuring fetal status
  • Maternal pulse oximetry deterioration

Mode of Delivery 5, 1

  • Vaginal delivery is preferred and associated with improved maternal outcomes
  • Cesarean delivery reserved for standard obstetric indications
  • Epidural analgesia strongly recommended in absence of thrombocytopenia 3

Special Management Considerations

HELLP Syndrome Recognition 2

  • Characterized by hemolysis, elevated liver enzymes (>2× normal), and low platelets (<100,000/μL) 3
  • Epigastric or right upper quadrant pain is hallmark symptom suggesting hepatic capsule distension 2
  • Maternal mortality rate 3.4% 2
  • Monitor glucose intraoperatively as severe hypoglycemia can occur 2

Pulmonary Edema Management 2

  • Drug of choice: IV nitroglycerin starting at 5 mcg/min, gradually increased every 3-5 minutes to maximum 100 mcg/min
  • Plasma volume expansion not recommended routinely

Postpartum Management

  • Continue magnesium sulfate for 24 hours after delivery or last seizure 4, 6
  • Close monitoring for at least 3 days postpartum as 25-30% of eclamptic seizures occur postpartum 1, 4
  • Monitor blood pressure every 4-6 hours for at least 3 days 4
  • Continue antihypertensives; taper slowly only after days 3-6 postpartum unless BP <110/70 mmHg 4
  • Avoid NSAIDs in women with preeclampsia/eclampsia, especially with acute kidney injury—use alternative analgesia 4
  • Check blood pressure and urine at 6 weeks postpartum 4
  • Assess for secondary causes of hypertension in women under 40 with persistent hypertension 4

Prevention Strategies for High-Risk Women

Low-dose aspirin (75-162 mg/day) should be initiated before 16 weeks' gestation (definitely before 20 weeks) for women with strong clinical risk factors. 5, 1

  • Evidence shows 15% reduction in preeclampsia incidence and 7% reduction in preterm deliveries 5
  • Supplemental calcium (1.2-2.5 g/day) if dietary intake likely low (<600 mg/day) 1

Common Pitfalls to Avoid

  • Do not attempt to diagnose "mild versus severe" preeclampsia clinically—all cases may become emergencies rapidly 2
  • Do not use serum uric acid or level of proteinuria as sole indication for delivery 2
  • Do not reduce antihypertensives if diastolic BP falls <80 mmHg 2
  • Do not use hydralazine as first-line agent as it was found inferior to other agents 5

Long-Term Counseling

  • Women with preeclampsia have increased lifetime cardiovascular risk and require long-term follow-up 1, 7
  • Regular exercise during pregnancy may help reduce likelihood of hypertension 1
  • Pregnancy serves as a window for identifying future cardiovascular health risks 7

References

Guideline

Management of Pre-eclampsia

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Guideline

Management of Severe Preeclampsia

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Research

Preeclampsia: an update.

Acta anaesthesiologica Belgica, 2014

Guideline

Management of Eclampsia

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Research

Pre-eclampsia.

Lancet (London, England), 2016

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.

Have a follow-up question?

Our Medical A.I. is used by practicing medical doctors at top research institutions around the world. Ask any follow up question and get world-class guideline-backed answers instantly.