What is the management approach for a pregnant woman diagnosed with pre-eclampsia?

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Management of Preeclampsia

All women diagnosed with preeclampsia at ≥37 weeks' gestation should undergo immediate delivery after maternal stabilization, while those with severe features require urgent blood pressure control with IV antihypertensives (target 110-140/85 mmHg) and magnesium sulfate for seizure prophylaxis regardless of gestational age. 1, 2, 3

Initial Assessment and Risk Stratification

Diagnostic Confirmation

  • Preeclampsia is defined as new-onset hypertension (≥140/90 mmHg) after 20 weeks' gestation, and while proteinuria was historically required, it is no longer mandatory for diagnosis 4, 5
  • Proteinuria is confirmed by ≥300 mg/24 hours, spot urine protein/creatinine ratio ≥30 mg/mmol (or 0.3 mg/mg), or ≥1+ on dipstick testing 4, 1
  • All cases of preeclampsia should be treated as potentially severe, as rapid progression to life-threatening complications can occur even with initially mild presentations 1, 3

Severity Assessment

Severe features include any of the following 1, 3, 5:

  • Severe hypertension: BP ≥160/110 mmHg on two occasions at least 15 minutes apart
  • Thrombocytopenia: platelets <100,000/μL
  • Elevated liver transaminases: >2 times upper limit of normal
  • Renal dysfunction: creatinine >1.1 mg/dL or doubling of baseline
  • Pulmonary edema
  • New-onset persistent severe headache unresponsive to medication
  • Visual disturbances (scotomata, cortical blindness)
  • Epigastric or right upper quadrant pain (suggests hepatic capsule distension or HELLP syndrome) 3, 5

Immediate Stabilization for Severe Preeclampsia

Blood Pressure Management

Urgent antihypertensive therapy must be initiated immediately when BP ≥160/110 mmHg persists for >15 minutes to prevent maternal cerebral hemorrhage 1, 3

First-line IV antihypertensive options 1, 3:

  • IV labetalol: 20 mg IV bolus, then 40 mg after 10 minutes, then 80 mg every 10 minutes (maximum cumulative dose 220 mg)
  • IV hydralazine: 5-10 mg IV every 20 minutes as needed
  • Oral nifedipine immediate-release: 10-20 mg orally, repeat in 20 minutes if needed (for non-severe hypertension or when IV access unavailable)

Target blood pressure: Systolic 110-140 mmHg and diastolic 85 mmHg (or at minimum <160/105 mmHg) 1, 3

Critical medication warnings 3:

  • Short-acting oral nifedipine should be avoided when combined with magnesium sulfate due to risk of uncontrolled hypotension
  • Sodium nitroprusside should only be used as last resort due to risk of fetal cyanide poisoning
  • ACE inhibitors, ARBs, and direct renin inhibitors are absolutely contraindicated due to severe fetotoxicity 3

Seizure Prophylaxis with Magnesium Sulfate

Magnesium sulfate must be administered immediately to all patients with severe preeclampsia or those with proteinuria plus severe hypertension or any neurological symptoms 1, 3, 6

Dosing regimen 6:

  • Loading dose: 4-5 g IV over 5 minutes (diluted in 250 mL of 5% dextrose or 0.9% normal saline)
  • Maintenance: 1-2 g/hour continuous IV infusion
  • Alternative regimen: After 4 g IV loading dose, give 4-5 g IM (10 mL of 50% solution) into each buttock, then 4-5 g IM into alternate buttocks every 4 hours as needed

Therapeutic serum magnesium level: 4-7.5 mEq/L (6 mg/100 mL is optimal for seizure control) 6

Critical monitoring for magnesium toxicity 3, 6:

  • Deep tendon reflexes before each dose (reflexes disappear at ~10 mEq/L)
  • Respiratory rate (respiratory paralysis may occur at ~10 mEq/L)
  • Urine output: maintain ≥100 mL/4 hours or >35 mL/hour via Foley catheter 3
  • Have calcium gluconate 1 g (10 mL of 10% solution) at bedside as antidote for magnesium toxicity 6

Important limitation: Continuous maternal administration beyond 5-7 days can cause fetal abnormalities 6

Comprehensive Laboratory and Fetal Assessment

Initial Laboratory Workup

Obtain immediately at diagnosis 1, 3:

  • Complete blood count with focus on hemoglobin and platelet count
  • Comprehensive metabolic panel: liver transaminases (AST/ALT), creatinine, uric acid
  • Peripheral blood smear if HELLP syndrome suspected (hemolysis, elevated liver enzymes, low platelets)
  • Spot urine protein/creatinine ratio

Ongoing monitoring: Repeat labs at least twice weekly, or more frequently with clinical deterioration 3

Fetal Assessment

Initial ultrasound evaluation 1, 2:

  • Fetal biometry to assess for growth restriction
  • Amniotic fluid volume assessment
  • Umbilical artery Doppler velocimetry

Ongoing fetal surveillance 1, 3:

  • Continuous electronic fetal heart rate monitoring
  • Repeat ultrasound every 2 weeks if initial assessment normal, more frequently if fetal growth restriction present
  • Daily fetal movement counts

Maternal Monitoring Requirements

Continuous assessment includes 1, 3:

  • Blood pressure monitoring (hourly in acute phase)
  • Oxygen saturation on room air (maternal early warning if <95%)
  • Hourly urine output via Foley catheter (target ≥100 mL/4 hours)
  • Assessment for symptoms: severe headache, visual changes, epigastric pain, shortness of breath
  • Clinical examination: deep tendon reflexes, clonus, mental status changes

Delivery Timing: Gestational Age-Based Algorithm

≥37 Weeks' Gestation

Immediate delivery is indicated after maternal stabilization 1, 2, 3

  • Induction of labor is preferred and associated with improved maternal outcomes 3, 7
  • Vaginal delivery is preferred unless cesarean indicated for standard obstetric reasons 2, 3

34-37 Weeks' Gestation

Without severe features: Expectant management with close monitoring is appropriate 1, 3

With severe features: Deliver after maternal stabilization 3, 5

  • Administer antenatal corticosteroids for fetal lung maturity if not previously given 5

<34 Weeks' Gestation

Conservative expectant management at a center with Maternal-Fetal Medicine expertise 3, 7

  • Administer antenatal corticosteroids for fetal lung maturity 5
  • Average prolongation is 7-10 days in carefully selected patients 7
  • This approach improves neonatal outcomes but requires intensive maternal and fetal monitoring 7

<24 Weeks' Gestation

Counsel regarding pregnancy termination 3

  • Expectant management is associated with high maternal morbidity with limited perinatal benefit 3, 7

Absolute Indications for Immediate Delivery (Any Gestational Age)

Deliver immediately regardless of gestational age if any of the following occur 1, 3, 7:

  • Inability to control BP despite ≥3 classes of antihypertensives in appropriate doses
  • Progressive thrombocytopenia or progressively abnormal liver/renal function tests
  • Pulmonary edema
  • Severe intractable headache, repeated visual scotomata, or eclamptic seizures
  • Placental abruption
  • Non-reassuring fetal status on continuous monitoring
  • Maternal oxygen saturation deterioration (<90%)
  • HELLP syndrome with deteriorating maternal condition

Special Considerations and Critical Pitfalls

HELLP Syndrome Recognition

HELLP syndrome is defined by 3, 5:

  • Hemolysis (peripheral blood smear, elevated LDH, decreased haptoglobin)
  • Elevated Liver enzymes (AST/ALT >2 times upper limit)
  • Low Platelets (<100,000/μL)

Maternal mortality rate is 3.4% 3

  • Epigastric or right upper quadrant pain is a hallmark symptom 3
  • Monitor glucose intraoperatively as severe hypoglycemia can occur 3

Management of Pulmonary Edema

Drug of choice: IV nitroglycerin (glycerol trinitrate) starting at 5 mcg/min, gradually increased every 3-5 minutes to maximum 100 mcg/min 3

  • Plasma volume expansion is NOT recommended routinely 1, 3

Common Pitfalls to Avoid

  • Do not underestimate disease severity based on "mild" classification—all preeclampsia can rapidly progress 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
  • Do not use serum uric acid or level of proteinuria as indication for delivery 1, 3
  • Do not delay delivery at ≥37 weeks based on non-reactive NST—delivery is indicated regardless of fetal testing results 2
  • Do not reduce antihypertensives if diastolic BP falls <80 mmHg 3
  • Do not use diuretics routinely—they further reduce plasma volume which is already contracted in preeclampsia 3

Postpartum Considerations

  • Continue magnesium sulfate for 24-48 hours postpartum in severe cases 8, 9
  • Continue antihypertensive therapy as needed postpartum
  • Preeclampsia is a risk factor for developing cardiovascular disease later in life and mandates long-term follow-up 5

Transfer and Coordination

For severe preeclampsia, consider transfer to specialized obstetric center 3:

  • Initiate magnesium sulfate and blood pressure control prior to transport
  • Coordinate with obstetric and anesthetic-intensivist teams at receiving facility
  • Involve emergency medical assistance service for medicalized transport

References

Guideline

Initial Management of Pre-eclampsia

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Guideline

Management of Mild Preeclampsia at 37 Weeks

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Guideline

Management of Severe Preeclampsia

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Research

Preeclampsia: an update.

Acta anaesthesiologica Belgica, 2014

Research

Management of preeclampsia.

Pregnancy hypertension, 2014

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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