Preeclampsia
Early Identification & Evidence-Based Management
MFM Clinical Update 2025
Epidemiology & Impact
- 2–8% of pregnancies in the United States
- Leading cause of maternal morbidity and mortality worldwide
- Disproportionate burden: Black women 60% higher risk
- Associated with preterm birth, IUGR, placental abruption
- Long-term cardiovascular risk for mother and offspring
ACOG Practice Bulletin #222, 2020
Pathophysiology
- Stage 1 (Early pregnancy): Abnormal placentation
• Inadequate trophoblast invasion
• Failure of spiral artery remodeling
- Stage 2 (Mid-late pregnancy): Maternal syndrome
• Endothelial dysfunction (↓ VEGF, ↑ sFlt-1, ↑ sEng)
• Systemic inflammation and oxidative stress
• Hypertension and end-organ damage
sFlt-1/PlGF ratio increasingly used for diagnosis and prediction
Diagnostic Criteria (ACOG 2019)
Blood Pressure
SBP ≥140 or DBP ≥90 mmHg on two occasions at least 4 hours apart after 20 weeks in previously normotensive woman
Plus ONE of:
- Proteinuria ≥300 mg/24h or protein/creatinine ≥0.3
- Thrombocytopenia (platelets <100,000)
- Renal insufficiency (Cr >1.1 or doubling of baseline)
- Elevated liver enzymes (2× upper limit)
- Pulmonary edema
- New-onset headache or visual symptoms
Preeclampsia with Severe Features
- Severe hypertension: SBP ≥160 or DBP ≥110 mmHg
- Thrombocytopenia: Platelets <100,000/μL
- Liver dysfunction: Transaminases 2× normal, RUQ pain
- Renal dysfunction: Creatinine >1.1 mg/dL or doubling
- Pulmonary edema
- Cerebral or visual symptoms: Persistent headache, scotomata
Severe features warrant closer monitoring and earlier delivery
Risk Stratification
High-Risk Factors (>8% risk)
- Prior preeclampsia (especially <34 weeks)
- Multifetal gestation
- Chronic hypertension
- Type 1 or 2 diabetes
- Renal disease
- Autoimmune disease (SLE, APS)
Moderate-Risk Factors
Nulliparity, obesity (BMI >30), family history, age ≥35, prior adverse pregnancy outcome, IVF, low socioeconomic status
First-Trimester Screening
FMF Algorithm (11-13+6 weeks)
- Maternal characteristics + history
- Mean arterial pressure (MAP)
- Uterine artery Doppler (pulsatility index)
- Serum PAPP-A and PlGF
Detection rate: ~75% for early preeclampsia (<37 weeks) with 10% false positive rate
ASPRE trial demonstrated effectiveness of this approach
Aspirin Prophylaxis
USPSTF & ACOG Recommendations (2021)
- Dose: 81-162 mg daily (consider 162 mg for high-risk)
- Timing: Initiate before 16 weeks (ideally 12 weeks)
- Continue until delivery
- Indication: ≥1 high-risk factor OR ≥2 moderate-risk factors
NNT: 72 to prevent one case of preeclampsia
ASPRE trial: 62% reduction in early preeclampsia with 150mg at bedtime
Antenatal Surveillance
Preeclampsia Without Severe Features
- BP monitoring 2× weekly (can be outpatient)
- Weekly labs (CBC, LFTs, creatinine)
- Fetal testing: NST/BPP 1-2× weekly starting at diagnosis
- Growth ultrasound every 3 weeks
Preeclampsia With Severe Features
- Inpatient management at ≥34 weeks
- Consider expectant management 23-33+6 weeks at tertiary center
- Daily labs, continuous or frequent BP monitoring
- Daily fetal testing
Acute Severe Hypertension Management
Goal: SBP 140-150 mmHg, DBP 90-100 mmHg within 30-60 minutes
First-Line Agents
| Medication |
Dose |
Notes |
| Labetalol IV |
20 mg → 40 mg → 80 mg q10min |
Max 220 mg total |
| Hydralazine IV |
5-10 mg q20min |
Max 20 mg total |
| Nifedipine PO |
10-20 mg q20min |
Immediate release |
ACOG recommends treating sustained SBP ≥160 or DBP ≥110 mmHg
Magnesium Sulfate for Seizure Prophylaxis
Indications
- Preeclampsia with severe features
- During labor and 24-48 hours postpartum
- Treatment and prevention of eclamptic seizures
Dosing
Loading: 4-6 g IV over 15-20 minutes
Maintenance: 2 g/hour continuous infusion
Monitoring
• Deep tendon reflexes (discontinue if absent)
• Respiratory rate >12/min
• Urine output >25 mL/hour
• Serum magnesium levels if renal insufficiency (goal 4-7 mEq/L)
Timing of Delivery
| Clinical Scenario |
Timing |
| Preeclampsia without severe features |
37 0/7 weeks |
| Preeclampsia with severe features |
34 0/7 weeks |
| HELLP syndrome |
34 0/7 weeks |
| Eclampsia |
Deliver after stabilization |
| Severe features + maternal instability |
Immediate delivery |
Betamethasone recommended <34 weeks; consider up to 36+6 weeks
HELLP Syndrome
Diagnostic Criteria
- Hemolysis (↑ LDH, ↑ bilirubin, ↓ haptoglobin, schistocytes)
- Elevated Liver enzymes (AST/ALT >2× normal)
- Low Platelets (<100,000/μL)
Management
- 10-20% may present without hypertension or proteinuria
- Delivery indicated at ≥34 weeks
- Consider dexamethasone if <34 weeks and expectant management attempted
- Monitor for DIC, liver hematoma/rupture, acute renal failure
Postpartum Management
Immediate Postpartum (0-72 hours)
- Continue magnesium sulfate 24-48 hours
- Monitor BP closely (peaks 3-6 days postpartum)
- Treat severe hypertension aggressively
- Monitor for postpartum preeclampsia/eclampsia
Preferred Antihypertensives
• Labetalol, nifedipine (safe for breastfeeding)
• Avoid methyldopa (slow onset), ACE-I/ARBs (use with caution in breastfeeding)
NSAIDs
Use with caution; may worsen hypertension and renal function
Long-Term Cardiovascular Risk
- 2-4× increased risk of cardiovascular disease
- 2× increased risk of stroke
- Risk of chronic hypertension, metabolic syndrome, diabetes
- Earlier age of cardiovascular events (40s-50s)
Postpartum Counseling
- Discuss long-term cardiovascular risk
- Recommend BP check at 7-10 days, 6 weeks, and annually
- Lifestyle modifications: diet, exercise, weight management
- Consider cardiology referral for early preeclampsia or recurrent disease
AHA 2021: Preeclampsia is independent CV risk factor
Recurrence Risk & Future Pregnancy
| Prior Outcome |
Recurrence Risk |
| Preeclampsia at term |
5-7% |
| Preeclampsia <34 weeks |
25-65% |
| Preeclampsia in 2 pregnancies |
32% |
| Severe preeclampsia |
Up to 40% |
Preconception Counseling
• Optimize chronic conditions
• Aspirin prophylaxis starting <16 weeks
• Consider first-trimester screening
• Enhanced surveillance in subsequent pregnancy
Clinical Pearls
- Diagnosis doesn't require proteinuria – other end-organ findings sufficient
- Headache + hyperreflexia doesn't predict seizure; magnesium still indicated
- BP can normalize between readings; don't dismiss diagnosis
- Platelets often first to fall – trend labs serially
- Postpartum hypertension peaks days 3-6, not immediately after delivery
- Delivery is curative for fetus, but maternal disease may progress 48-72h
Summary & Clinical Action Items
- Screen early: Risk stratify at first prenatal visit
- Prevent when possible: Aspirin <16 weeks for high-risk patients
- Diagnose accurately: New hypertension + end-organ involvement
- Manage severe features: Control BP, give MgSO4, deliver appropriately
- Time delivery correctly: Balance maternal/fetal risks
- Follow long-term: Counsel on cardiovascular risk, ensure ongoing care
Evidence-based care can significantly reduce maternal morbidity and improve outcomes