What is the role of intravenous (IV) magnesium sulphate in the management of eclampsia?

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Last updated: July 10, 2025View editorial policy

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Role of Intravenous Magnesium Sulphate in Eclampsia Management

Intravenous magnesium sulphate is the first-line treatment for eclampsia, both for treating active seizures and preventing recurrent seizures, with clear evidence showing it approximately halves the seizure rate compared to other anticonvulsants. 1

Indications and Mechanism

Magnesium sulphate is indicated for:

  • Treatment of active eclamptic seizures
  • Prevention of recurrent seizures in women with eclampsia
  • Seizure prophylaxis in severe pre-eclampsia

Magnesium works primarily through:

  • Central nervous system depression
  • Peripheral neuromuscular blockade
  • Cerebral vasodilation

Dosing Regimen

The FDA-approved dosing for eclampsia includes 2:

Initial Loading Dose

  • 4-5g IV in 250mL of 5% Dextrose or 0.9% Sodium Chloride infused over 15-20 minutes

Maintenance Options

  1. IV Continuous Infusion:

    • 1-2g/hour by controlled infusion pump
    • Continue until 24 hours after delivery or last seizure
  2. IM Regimen (Pritchard):

    • 10g IM initially (5g in each buttock) following IV loading dose
    • Then 5g IM every 4 hours in alternating buttocks

The ISSHP recommends using dosing regimens from the Eclampsia and MAGPIE trials 1.

Therapeutic Monitoring

Careful monitoring is essential to prevent toxicity 2, 3:

  • Therapeutic range: 1.8-3.0 mmol/L (4.5-7.5 mg/dL)
  • Monitor:
    • Deep tendon reflexes (patellar reflex) - first sign of toxicity when lost
    • Respiratory rate (should be >12/min)
    • Urine output (should be >30 mL/hour)
    • Level of consciousness

Toxicity Warning Signs

Serum Mg Level Clinical Manifestation
3.5-5 mmol/L Loss of patellar reflex
5-6.5 mmol/L Respiratory depression
>7.5 mmol/L Cardiac conduction abnormalities
>12.5 mmol/L Cardiac arrest

Duration of Treatment

  • Continue MgSO₄ for 24 hours after delivery or last seizure 1
  • Some evidence suggests that shorter duration may be sufficient if the patient has received at least 8g before delivery, but most guidelines still recommend 24 hours postpartum 1

Concurrent Management

  • Control blood pressure with IV labetalol or oral nifedipine to maintain BP <160/105 mmHg 1
  • Limit total fluid intake to 60-80 mL/hour to prevent pulmonary edema 1
  • Monitor fetal heart rate (caution with labetalol: cumulative dose should not exceed 800 mg/24h to prevent fetal bradycardia) 1
  • Consider delivery after maternal stabilization 1

Efficacy Compared to Other Agents

Magnesium sulphate is superior to other anticonvulsants:

  • Compared to phenytoin: 66% reduction in recurrent seizures (RR 0.34) 4
  • Better maternal and fetal outcomes than diazepam or phenytoin 4, 5

Common Pitfalls and Caveats

  1. Renal function monitoring: Magnesium is primarily excreted by kidneys; dose adjustment needed in renal impairment 2

  2. Calcium gluconate availability: Always have 10% calcium gluconate (10mL) readily available as antidote for magnesium toxicity

  3. Prolonged use risks: Continuous administration beyond 5-7 days can cause fetal bone abnormalities 2

  4. Aluminum toxicity: Contains aluminum that may reach toxic levels with prolonged administration in patients with impaired kidney function 2

  5. Drug interactions: Enhanced effects with CNS depressants, muscle relaxants, and calcium channel blockers

  6. Monitoring gaps: Failure to monitor reflexes, respiration, and urine output can lead to undetected toxicity

  7. Alternative regimens: Low-dose IV regimens (0.6g/hour) may be equally effective with potentially fewer side effects 6

Magnesium sulphate remains the cornerstone of eclampsia management, with strong evidence supporting its efficacy and safety when properly administered and monitored.

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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