Eclampsia
Eclampsia is the occurrence of generalised tonic-clonic seizures in a woman with pre-eclampsia, representing a life-threatening obstetric emergency requiring immediate treatment.
Key Facts
Eclampsia complicates approximately 1 in 2,000 pregnancies in the UK Magnesium sulphate is the first-line anticonvulsant (4g IV loading dose over 5-15 minutes, then 1g/hr infusion) per NICE NG133 38% of eclamptic seizures occur postpartum, 18% antepartum, and 44% intrapartum MAGPIE trial demonstrated magnesium sulphate halves the risk of eclampsia in pre-eclamptic women Labetalol is first-line antihypertensive in pregnancy (NICE NG133); target BP <150/100 mmHg Delivery is the definitive treatment; timing depends on gestation and maternal/fetal condition Recurrence risk of eclampsia in subsequent pregnancies is approximately 2-5% Monitor for magnesium toxicity: loss of patellar reflexes, respiratory depression (therapeutic range 2-4 mmol/L)
Overview
Key Facts
Eclampsia is defined as the occurrence of one or more generalised tonic-clonic seizures in association with pre-eclampsia. It is a medical emergency with significant maternal and fetal mortality if not promptly managed.
Epidemiology
- Incidence: approximately 1 in 2,000 pregnancies in the UK
- UK maternal mortality from eclampsia/pre-eclampsia: approximately 0.3 per 100,000 maternities
- More common in primigravidae, multiple pregnancies, and extremes of maternal age
- Can occur antepartum (38%), intrapartum (18%), or postpartum (44%)
Aetiology
- Arises from severe pre-eclampsia with cerebral vasospasm and endothelial dysfunction
- Risk factors include: nulliparity, pre-existing hypertension, chronic kidney disease, autoimmune disease (SLE, antiphospholipid syndrome), diabetes, BMI >35, age >40, multiple pregnancy, family history of pre-eclampsia
- Abnormal placentation with defective spiral artery remodelling is the underlying pathological process
Pathophysiology
- Inadequate trophoblastic invasion of spiral arteries leads to placental ischaemia
- Release of anti-angiogenic factors (sFlt-1, soluble endoglin) causes widespread endothelial dysfunction
- Cerebral vasospasm and blood-brain barrier disruption lead to cerebral oedema and seizures
- Posterior reversible encephalopathy syndrome (PRES) is the radiological correlate on MRI
Clinical Presentation
Typical Presentation
- Generalised tonic-clonic seizures in a pregnant or recently delivered woman
- Often preceded by symptoms of severe pre-eclampsia: severe headache, visual disturbance (blurred vision, scotomata, flashing lights), epigastric/right upper quadrant pain
- Hypertension (BP ≥140/90 mmHg) with proteinuria (≥300mg/24h or PCR ≥30mg/mmol)
Prodromal Symptoms
- Severe headache unresponsive to simple analgesia
- Visual disturbance (photopsia, scotomata, cortical blindness)
- Epigastric or right upper quadrant pain (hepatic capsule distension)
- Hyperreflexia and clonus (≥3 beats)
- Rapidly progressive oedema
Red Flags
- Seizures at any point in pregnancy or within 6 weeks postpartum
- Systolic BP >160 mmHg or diastolic >110 mmHg
- HELLP syndrome features (haemolysis, elevated liver enzymes, low platelets)
- Papilloedema
- Signs of placental abruption
- Oliguria (<0.5 mL/kg/hr)
- Glasgow Coma Scale <14
Differential Diagnosis
| Diagnosis | Key Features | Investigation |
|---|---|---|
| Epilepsy | Known history, no hypertension/proteinuria | EEG, serum prolactin |
| Cerebral venous sinus thrombosis | Headache, focal neurology, may have seizures | CT/MR venography |
| Intracranial haemorrhage | Sudden severe headache, focal neurology | CT head |
| Meningitis/encephalitis | Fever, neck stiffness, photophobia | LP, blood cultures |
| Posterior reversible encephalopathy syndrome | Visual disturbance, headache, seizures | MRI brain |
| Thrombotic thrombocytopenic purpura | Thrombocytopenia, MAHA, neurological features | Blood film, ADAMTS13 |
| Hypoglycaemia | Confusion, seizures, diaphoresis | Capillary blood glucose |
Diagnosis / Investigation
Bedside
- Blood pressure monitoring (every 15 minutes during acute phase)
- Urinalysis (proteinuria quantification - PCR or 24h collection)
- Continuous CTG for fetal monitoring
- Fluid balance chart (strict input/output)
- Capillary blood glucose
Bloods
- FBC (particularly platelet count - <100 × 10⁹/L suggests HELLP)
- U&Es (renal function - uric acid, creatinine)
- LFTs (ALT/AST elevation suggests HELLP)
- Coagulation screen (DIC screen)
- Blood film (for fragmented red cells/schistocytes)
- Group and save / crossmatch
- Serum magnesium levels (therapeutic range 2-4 mmol/L)
Imaging
- CT head if atypical features or prolonged post-ictal state
- MRI brain if suspecting PRES or other intracranial pathology
- Ultrasound for fetal assessment (growth, liquor volume, Dopplers)
Special Tests
- PlGF-based testing if <37 weeks (NICE NG133)
- Urine protein:creatinine ratio
- Arterial blood gas if respiratory compromise
Management
Non-pharmacological
- Multidisciplinary approach: obstetrics, anaesthetics, midwifery, neonatology
- Left lateral position during seizure
- Airway management and high-flow oxygen
- Monitor in high-dependency setting
- Strict fluid balance (limit IV fluids to 80 mL/hr to reduce pulmonary oedema risk)
Pharmacological
- Magnesium sulphate: 4g IV loading dose over 5-15 minutes, followed by 1g/hr infusion for 24 hours (MAGPIE trial evidence)
- Recurrent seizures: further 2g IV magnesium sulphate bolus
- Antihypertensives: Labetalol 200mg PO or 50mg IV (first-line per NICE NG133); nifedipine 10-20mg PO (second-line); hydralazine 5mg IV (third-line)
- Target BP <150/100 mmHg
- Antidote for magnesium toxicity: calcium gluconate 10% 10 mL IV over 10 minutes
Surgical/Interventional
- Delivery is the definitive treatment
- If ≥34 weeks: plan delivery within 24-48 hours
- If <34 weeks: consider corticosteroids (betamethasone 12mg IM × 2 doses, 24h apart) for fetal lung maturation if delivery can be safely delayed
- Emergency caesarean section if maternal or fetal compromise
Referral Criteria
- All cases require consultant obstetrician and anaesthetist involvement
- HDU/ITU admission for ventilatory support or multi-organ failure
- Follow-up at 6-8 weeks postpartum with BP and proteinuria check
- Referral to specialist hypertension clinic if persistent hypertension
Prognosis
- UK maternal mortality from eclampsia: approximately 1-2% (has fallen with improved management)
- Perinatal mortality: 5-12% (higher with preterm delivery)
- 35% of women develop complications: HELLP syndrome, DIC, renal failure, pulmonary oedema, ARDS
- Risk of recurrence in subsequent pregnancy: 2-5% for eclampsia, 15-25% for pre-eclampsia
- Long-term cardiovascular risk is increased: 2-4× risk of chronic hypertension, 2× risk of ischaemic heart disease
- Aspirin 75-150mg from 12 weeks in subsequent pregnancies reduces pre-eclampsia risk by 17% (NICE NG133)
Other Relevant Information
MAGPIE Trial Summary
| Feature | Detail |
|---|---|
| Population | 10,141 women with pre-eclampsia |
| Intervention | Magnesium sulphate vs placebo |
| Result | 58% reduction in eclampsia risk |
| NNT | 63 for moderate pre-eclampsia, 109 overall |
Severity Classification
| Feature | Mild Pre-eclampsia | Severe Pre-eclampsia |
|---|---|---|
| BP | 140/90 - 159/109 | ≥160/110 |
| Proteinuria | PCR 30-99 mg/mmol | PCR ≥100 mg/mmol |
| Symptoms | None | Headache, visual disturbance, epigastric pain |
| Platelets | Normal | <100 × 10⁹/L |
Magnesium Sulphate Monitoring
| Parameter | Target/Action |
|---|---|
| Patellar reflexes | Must be present (loss = toxicity) |
| Respiratory rate | >16/min |
| Urine output | >25 mL/hr |
| Serum Mg²⁺ | 2-4 mmol/L (therapeutic range) |