Pre-Eclampsia & Eclampsia
Hypertensive disorders of pregnancy are major causes of maternal morbidity and mortality. In ED: recognise early, control BP, prevent seizures, and arrange urgent obstetric management.
Pregnancy + BP ≥ 140/90
Ask about headache & visual change
Think HELLP
Magnesium = anti-seizure drug of choice
Foundations & Definitions
BasicsHypertension occurs in ~8% of pregnancies. Key categories:
- Gestational hypertension: new BP ≥ 140/90 mmHg after 20 weeks’ gestation, no proteinuria, normal labs.
- Pre-eclampsia: gestational hypertension + evidence of organ involvement, classically proteinuria (>300 mg/24 h) but may also be thrombocytopenia, renal or liver dysfunction, pulmonary oedema, or neurological symptoms.
- Severe features: BP ≥ 160/110 mmHg and/or significant organ dysfunction (severe headache, visual disturbance, epigastric/RUQ pain, oliguria, pulmonary oedema, low platelets, elevated LFTs).
- Eclampsia: generalised tonic–clonic seizures in a woman with pre-eclampsia (antepartum, intrapartum or postpartum).
- Chronic hypertension: known before pregnancy or noted before 20 weeks or persisting > 6 weeks postpartum; may have superimposed pre-eclampsia.
Key ED rule: Any pregnant or postpartum woman with headache, visual symptoms, epigastric pain, or seizure must have BP checked and urine protein considered.
Pathophysiology & Major Complications
Why It’s DangerousPathophysiology
- Abnormal placentation → endothelial dysfunction, vasospasm and leaky capillaries.
- Systemic vasoconstriction and microthrombosis → multi-organ injury (brain, liver, kidney, placenta).
- Eclampsia involves cerebral oedema, ischaemia and loss of autoregulation → seizures.
Complications
- HELLP syndrome: Haemolysis, Elevated Liver enzymes, Low Platelets – variant of severe pre-eclampsia.
- Placental abruption, intra-uterine growth restriction, fetal distress and prematurity.
- Cerebral haemorrhage, pulmonary oedema, renal failure, DIC.
- Maternal death or severe long-term morbidity if not recognised early.
Clinical Features
Presentation- Pre-eclampsia (without severe features):
- BP ≥ 140/90 mmHg after 20 weeks on at least two readings.
- Proteinuria or other evidence of organ involvement may be minimal.
- Often asymptomatic or mild symptoms (mild headache, oedema).
- Pre-eclampsia with severe features:
- BP ≥ 160/110 mmHg.
- Severe or persistent headache, visual disturbances (“flashing lights”, blurring), hyperreflexia or clonus.
- Epigastric or right upper quadrant pain (capsular stretch from liver involvement).
- Oliguria, rising creatinine, pulmonary oedema, low platelets, rising LFTs.
- Eclampsia: generalised tonic–clonic seizure (before, during or after delivery), often preceded by severe headache, visual symptoms or agitation.
Red flags: BP ≥ 160/110, severe headache, visual symptoms, RUQ pain, altered mental status, hyperreflexia/clonus,
platelets dropping, or any seizure → treat as severe pre-eclampsia/eclampsia and escalate immediately.
ED Algorithm
Flow- Assess ABC, place in left lateral position; give high-flow oxygen if unwell; attach monitoring (BP, pulse, SpO₂).
- Check gestational age and obstetric history; confirm pregnancy or recent delivery (up to 6 weeks postpartum).
- Measure BP correctly; repeat to confirm. Check urine (dipstick protein if lab unavailable).
- Take bloods: FBC, platelets, U&E/creatinine, LFTs, coagulation profile; consider magnesium level if on MgSO₄.
- If seizure or very high BP:
- Protect airway, give oxygen, manage seizure (MgSO₄ – see below).
- Start rapid-acting antihypertensive if BP ≥ 160/110 mmHg.
- Call obstetrics/anaesthetics early – definitive treatment is delivery of the fetus and placenta at an appropriate facility.
- Consider urgent transfer to higher level of care/ICU if available and safe.
Diagnostic Workup
Investigations- Vital signs including BP trend; strict input/output charting (urine catheter if severe).
- Urine dipstick for protein; 24-hour protein or protein–creatinine ratio if available (not ED-urgent but note if done).
- Bloods:
- FBC & platelets (look for anaemia, thrombocytopenia, HELLP).
- U&E/creatinine (renal involvement).
- LFTs (AST/ALT, LDH – liver involvement/HELLP).
- Coagulation profile if severe disease, HELLP, or abruption suspected.
- Consider CT head/MRI if atypical features, focal neurology or poor recovery after seizure to exclude haemorrhage or thrombosis (once stable and in consultation with obstetrics/neurology).
Acute Blood Pressure Control
AntihypertensivesGoal in ED: rapidly reduce dangerously high BP (≥ 160 systolic or ≥ 110 diastolic) to safer levels (e.g. < 150/100) without dropping perfusion abruptly.
- Labetalol (IV)
- Common first-line agent (if no asthma, heart block, or severe bradycardia).
- Example regimen: 20 mg IV bolus over 2 minutes; if insufficient, repeat with 40 mg then 80 mg at 10–20 minute intervals as needed, up to a protocol-defined maximum.
- Hydralazine (IV)
- Alternative or used where labetalol unavailable/contraindicated.
- Example: 5–10 mg IV slowly; repeat every 20–30 minutes as needed, guided by BP and fetal status.
- Nifedipine (oral)
- Short-acting oral nifedipine (e.g. 10 mg) may be used where IV access or IV agents are not immediately available; monitor BP closely.
- Always follow your local obstetric/anaesthetic protocol for exact doses and targets.
Important: Avoid dropping BP too low or too quickly – aim for controlled reduction, maintaining uteroplacental perfusion.
Eclampsia & Magnesium Sulfate
SeizuresMagnesium sulfate (MgSO₄) is the drug of choice to prevent and treat eclamptic seizures.
Initial Seizure Management
- Position patient in left lateral position; protect airway and prevent injury.
- Give oxygen; suction as needed; prepare for intubation if prolonged or recurrent seizures, or low GCS.
Magnesium Sulfate Regimen (example)
- Loading dose: 4–6 g IV over 15–20 minutes.
- Maintenance: 2–3 g/hour IV infusion, usually for at least 24 hours after last seizure or delivery (follow local protocol).
- Monitor:
- Respiratory rate, oxygen saturation.
- Patellar reflexes.
- Urine output (> 25–30 mL/hour).
- Signs of magnesium toxicity: loss of reflexes, respiratory depression, bradycardia.
- Antidote for toxicity: 10 mL of 10% calcium gluconate IV given slowly (as per local protocol) and stop infusion.
Benzodiazepines may be used if seizures persist while arranging MgSO₄, but magnesium remains the primary agent.
Fluids & Supportive Care
Balance- Fluids: use cautiously – pre-eclamptic patients are intravascularly depleted but leaky; at risk of pulmonary oedema.
- Avoid routine diuretics; reserve for pulmonary oedema under specialist guidance.
- Typical approach: controlled IV fluids (e.g. ~80–100 mL/hour) with strict input/output charting – follow local protocol.
- Consider ICU/HDU admission for severe disease, eclampsia, HELLP, or organ failure.
Definitive Management & Disposition
Next Steps- Definitive treatment of pre-eclampsia/eclampsia is delivery of the fetus and placenta at an appropriate facility.
- Timing and mode of delivery depend on gestational age, maternal and fetal condition – decided by obstetric team.
- ED role:
- Resuscitate and stabilise (BP control, MgSO₄, airway/fluids).
- Initiate investigations to identify severity and complications.
- Communicate clearly with obstetrics/anaesthetics/ICU and prepare for transfer if needed.
- Remember postpartum eclampsia can occur up to 6 weeks after delivery – treat the same way (MgSO₄ + BP control + obstetric review).
Check BP in all pregnant/postpartum patients with headache or seizure
BP ≥ 160/110 → treat urgently
Magnesium sulfate prevents and treats seizures
Definitive treatment = delivery
Documentation & Handover
Safety- Record:
- Gestational age, parity, key antenatal history.
- Serial BP readings, symptoms (headache, visual change, RUQ pain, oedema, seizures).
- Medications given (antihypertensives, MgSO₄: dose and time), fluids, and investigation results.
- Provide a structured handover to obstetric/ICU teams, including trends and response to treatment.