magnesium sulfate (parenteral)
General
High Alert Medication: This medication bears a heightened risk of causing significant patient harm when it is used in error.
Pronunciation:
mag-nee-zhum sul-fate
Ther. Class.
mineral and electrolyte replacements/supplements
Pharm. Class.
minerals electrolytes
Indications
- Treatment/prevention of hypomagnesemia.
- Prevention and treatment of seizures associated with severe eclampsia or pre-eclampsia.
Unlabeled Use(s):
- Treatment of torsades de pointes.
- Adjunctive treatment for bronchodilation in moderate to severe acute asthma.
Action
- Essential for the activity of many enzymes.
- Plays an important role in neurotransmission and muscular excitability.
Therapeutic Effect(s):
- Replacement in deficiency states.
- Resolution of eclampsia.
Pharmacokinetics
Absorption: IV administration results in complete bioavailability; well absorbed from IM sites.
Distribution: Widely distributed to tissues
Metabolism and Excretion: Excreted primarily by the kidneys.
Half-life: Unknown.
TIME/ACTION PROFILE (anticonvulsant effect)
ROUTE | ONSET | PEAK | DURATION |
---|---|---|---|
IM | 60 min | unknown | 3–4 hr |
IV | immediate | unknown | 30 min |
Contraindication/Precautions
Contraindicated in:
- Hypermagnesemia;
- Hypocalcemia;
- Anuria;
- Heart block.
Use Cautiously in:
- Renal impairment;
- OB: Avoid using for more than 5–7 days for preterm labor (may ↑ risk of hypocalcemia and bone changes in newborn); avoid continuous use during active labor or within 2 hr of delivery due to potential for magnesium toxicity in newborn;
- Geri: Older adults may require ↓ dosage due to age-related ↓ in renal function.
Adverse Reactions/Side Effects
CV: arrhythmias, bradycardia, hypotension
Derm: flushing, sweating
GI: diarrhea
Metabolic: hypothermia
MS: muscle weakness
Neuro: drowsiness
Resp: ↓ respiratory rate
* CAPITALS indicate life-threatening.
Underline indicate most frequent.
Interactions
Drug-Drug
May potentiate calcium channel blockers and neuromuscular blocking agents.
Route/Dosage
Treatment of Deficiency
IM IV (Adults): Severe deficiency: 8–12 g/day in divided doses; Mild deficiency: 1 g every 6 hr for 4 doses or 250 mg/kg over 4 hr.
IM IV (Children >1 mo): 25–50 mg/kg/dose every 4–6 hr for 3–4 doses (max single dose = 2 g).
IV (Neonates): 25–50 mg/kg/dose every 8–12 hr for 2–3 doses.
Seizures Associated With Eclampsia/Pre-Eclampsia
IV (Adults): 4–6 g loading dose over 15–30 min at onset of labor or induction/cesarean delivery, followed by 1–2 g/hr continuous infusion for ≥24 hr after delivery (max infusion rate = 3 g/hr). If seizure occurs while receiving magnesium, an additional bolus of 2–4 g may be administered over ≥5 min. Max dose = 40 g/24 hr.
IM (Adults): 10 g loading dose administered as 5 g in each buttock at onset of labor or induction/cesarean delivery, followed by 5 g every 4 hr for ≥24 hr after delivery.
Torsades de Pointes
IV (Adults): 1–2 g over 15 min. If no response or torsade de pointes recurs, may repeat dose up to a total of 4 g in 1 hr; may follow with a continuous IV infusion of 0.5–1 g/hr.
IV (Infants and Children): 25–50 mg/kg/dose (max dose = 2 g).
Bronchodilation
IV (Adults): 2 g single dose.
IV (Children): 25 mg/kg/dose (max dose = 2 g).
Parenteral Nutrition
IV (Adults): 4–24 mEq/day.
IV (Children): 0.25–0.5 mEq/kg/day.
Availability (generic available)
Solution for injection (8.1 mEq Mg/g): 500 mg/mL (50%)
Premixed infusion: 1 g/100 mL, 2 g/50 mL, 4 g/50 mL, 4 g/100 mL, 20 g/500 mL, 40 g/1000 mL
Assessment
- Hypomagnesemia/Anticonvulsant: Monitor BP, HR, respirations, and ECG frequently during administration. Respirations should be >16/min before each dose.
- Monitor neurologic status before and throughout therapy. Institute seizure precautions. Patellar reflex (knee jerk) should be tested before each dose. If response is absent, no additional doses should be administered until positive response is obtained.
- Pedi: Monitor newborn for hypotension, hyporeflexia, and respiratory depression if mother has received magnesium sulfate.
Lab Test Considerations:
Monitor serum magnesium levels and renal function periodically.
Implementation
- High Alert: Accidental overdose of IV magnesium has resulted in serious patient harm and death. Have second practitioner independently double-check original order, dose calculations, and infusion pump settings. Do not confuse milligram (mg), gram (g), or milliequivalent (mEq) doses.
- IM IM route should only be used when unable to establish venous access. Administer deep IM. Administer subsequent injections in alternate sides. Dilute to a concentration of 200 mg/mL before injection.
IV Administration
- Vesicant: Magnesium sulfate is a vesicant. If extravasation occurs, immediately stop infusion. Leave needle/cannula in place temporarily but do not flush the line. Gently aspirate extravasated solution; then remove needle/cannula. Elevate patient's extremity and apply dry cold compresses.
- IV Push: Dilution: 50% solution must be diluted in 0.9% NaCl or D5W to a concentration of ≤20% prior to administration. Concentration: ≤20%.
- Rate: Administer over several min at a rate not to exceed 150 mg/min. In patients not in cardiac arrest, rapid administration may cause hypotension and asystole.
- Intermittent Infusion: Dilution: 50% solution must be diluted in 0.9% NaCl or D5W to a concentration of ≤20% prior to administration. Concentration: ≤20%.
- Rate: For ventricular tachycardia/torsade: Infuse over 10–20 min; rapid infusion may cause hypotension. For severe asthma exacerbation: Infuse over 15–60 min.
- Continuous Infusion: Dilution: Dilute in D5W, 0.9% NaCl, or LR. Concentration: 0.5 mEq/mL (60 mg/mL) (may use max concentration of 1.6 mEq/mL) (200 mg/mL) in fluid-restricted patients.
- Rate: Infuse over 2–4 hr. Do not exceed a rate of 1 mEq/kg/hr (125 mg/kg/hr). When rapid infusions are needed (severe asthma or torsade de pointes), may infuse over 10–20 min.
- Y-Site Compatibility:
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- potassium acetate
- potassium chloride
- procainamide
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- aminophylline
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- calcium chloride
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Patient/Family Teaching
- Explain purpose of medication to patient and caregivers.
- Rep: Monitor vital signs, oxygen saturation, respiration, deep tendon reflexes, level of consciousness, fetal HR, maternal uterine activity, and renal function when used during pregnancy. Monitor magnesium concentrations every 4 hr in patients with renal impairment (every 2 hr if serum magnesium is elevated). Breast milk concentrations are ↑ for only 24 hr after end of therapy.
Evaluation/Desired Outcomes
- Replacement in deficiency states.
- Resolution of eclampsia.