Mannitol
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Last updated: June 2025
For educational purposes only
Clinical Reference
# Mannitol
## Overview
- **Classification**: Osmotic Diuretic
- **Mechanism**: Increases plasma osmolarity, drawing water from extravascular spaces (including brain) into the intravascular space, increasing blood volume and renal blood flow.
## Primary Indications
1. **Reduction of Intracranial Pressure (ICP)** - Due to cerebral edema
2. **Reduction of Intraocular Pressure (IOP)** - Prior to ophthalmic surgery
3. **Promotion of Diuresis** - In prevention and treatment of oliguric phase of acute renal failure
## Adult Dosing
### Standard Dosing
**Reduction of ICP/IOP**
- **Dose**: **0.25-1 g/kg** (typically as 20% solution)
- **Frequency**: Every **6-8 hours** as needed
- **Route**: Intravenous infusion over **30-60 minutes**
- **Maximum**: **200 g/24 hours**
**Promotion of Diuresis (Oliguria Prophylaxis/Treatment)**
- **Test Dose**: **0.2 g/kg** IV over **3-5 minutes**
- **If diuresis occurs (30-50 mL/hr for 2-3 hours)**:
- **Dose**: **0.2-0.5 g/kg**
- **Frequency**: Every **4-6 hours** as needed
- **Route**: Intravenous infusion over **30-60 minutes**
- **Maximum**: **100 g/24 hours**
### Dose Adjustments
- **Renal Impairment**:
- **CrCl < 30 mL/min**: Use with extreme caution or contraindicated. Risk of accumulation and worsening heart failure.
- If used, start with a test dose. Discontinue if diuresis does not occur.
- **Hepatic Impairment**: No specific dose adjustments required.
- **Elderly Patients**:
- Start at lower end of dosing range due to potential for decreased renal function.
- Monitor closely for dehydration and electrolyte imbalance.
## Pediatric Dosing
### Neonates (0-28 days)
- **Indication**: Rarely used, consider only in life-threatening cerebral edema.
- **Dose**: **0.25-0.5 g/kg/dose** (e.g., 20% solution)
- **Frequency**: Every **6-8 hours** if absolutely necessary
- **Route**: Intravenous infusion over **20-30 minutes**
- **Maximum**: **1 g/kg/day**
- **Special Notes**: High risk of IVH, rebound ICP, and electrolyte disturbances due to immature blood-brain barrier. Monitor vital signs and fluid status diligently.
### Infants (1-12 months)
- **Indication**: Cerebral edema/increased ICP.
- **Test Dose**: **0.2 g/kg** IV over **3-5 minutes**
- **Full Dose**: **0.25-1 g/kg/dose** (e.g., 20% solution)
- **Frequency**: Every **6-8 hours** as needed
- **Route**: Intravenous infusion over **30-60 minutes**
- **Maximum**: **1.5 g/kg/day** or **50 g/day**, whichever is less.
### Children (1-12 years)
- **Indication**: Cerebral edema/increased ICP.
- **Test Dose**: **0.2 g/kg** IV over **3-5 minutes**
- **Full Dose**: **0.25-1 g/kg/dose** (e.g., 20% solution)
- **Frequency**: Every **6-8 hours** as needed
- **Route**: Intravenous infusion over **30-60 minutes**
- **Maximum**: **1.5 g/kg/day** or **100 g/day**, whichever is less.
### Adolescents (13-18 years)
- **Dose**: Generally follow adult dosing for respective indications.
- **Route**: Intravenous infusion over **30-60 minutes**
- **Maximum**: **200 g/24 hours** for ICP/IOP; **100 g/24 hours** for diuresis.
## Safety Information
### Contraindications
- **Absolute**: Anuria (unless test dose is negative), severe dehydration, active intracranial bleeding (unless prior to craniotomy), severe pulmonary congestion or edema, progressive heart failure.
- **Relative**: Severe renal disease, significant fluid/electrolyte imbalance.
### Common Adverse Effects
- **Very Common (>10%)**: Fluid/electrolyte imbalance (dehydration, hyponatremia, hypernatremia, hyperkalemia), thirst, headache, nausea, vomiting.
- **Common (1-10%)**: Dizziness, blurred vision, chills, hypotension, skin rash.
- **Serious but Rare**: Rebound ICP, acute kidney injury (osmotic nephrosis), congestive heart failure, pulmonary edema, anaphlaxis.
### Key Drug Interactions
- **Loop Diuretics**: Enhanced diuretic and natriuretic effects. Monitor for excessive fluid/electrolyte loss.
- **Nephrotoxic Drugs**: May increase risk of renal toxicity, especially with prolonged use. Monitor renal function closely.
- **Digoxin**: Mannitol-induced hypokalemia can potentiate digoxin toxicity. Monitor potassium and digoxin levels.
## Monitoring & Follow-up
- **Before Treatment**: Baseline serum electrolytes (Na, K), renal function (BUN, Cr), serum osmolality, and fluid status.
- **During Treatment**:
- **ICP/IOP**: Neurological status, ICP measurements (if available), IOP.
- **Fluid Balance**: Strict intake and output, daily weights.
- **Electrolytes**: Serum Na, K, Mg, Cl, serum osmolality every **4-6 hours** or as clinically indicated.
- **Renal Function**: BUN, Cr daily.
- **Clinical Signs**: Watch for signs of dehydration (e.g., dry mucous membranes, decreased skin turgor), worsening pulmonary edema (e.g., dyspnea, crackles), or rebound ICP (e.g., deteriorating mental status, pupillary changes).
## Clinical Pearls
- 💡 **Filter Required**: Always administer mannitol solutions (especially 20% or 25%) using a **filter needle** during preparation and an **in-line filter** during infusion to prevent infusion of mannitol crystals.
- 💡 **Warm to Dissolve**: If crystals are present, warm the solution in a warm water bath and shake vigorously. Cool to body temperature before administration.
- 💡 **Rebound Effect**: Monitor for rebound increases in ICP 6-10 hours post-dose, especially if blood-brain barrier is disrupted.
- 💡 **Fluid Status**: Carefully assess hydration status and correct dehydration before mannitol administration. Over-rapid infusion can exacerbate hypotension.
> **⚠️ Important**: This information is for educational purposes only. Always consult current prescribing information, local guidelines, and clinical judgment before prescribing.