Medical term:
Resectisol
mannitol
[man´ĭ-tol]mannitol
Pharmacologic class: Osmotic diuretic
Therapeutic class: Diuretic
Pregnancy risk category C
Action
Increases osmotic pressure of plasma in glomerular filtrate, inhibiting tubular reabsorption of water and electrolytes (including sodium and potassium). These actions enhance water flow from various tissues and ultimately decrease intracranial and intraocular pressures; serum sodium level rises while potassium and blood urea levels fall. Also protects kidneys by preventing toxins from forming and blocking tubules.
Availability
Injection: 5%, 10%, 15%, 20%, 25%
Solution: 5 g/100 ml
Indications and dosages
➣ Test dose for marked oliguria or suspected inadequate renal function
Adults: 0.2 g/kg I.V. infusion (approximately 50 ml of 25% solution, 75 ml of 20% solution, or 100 ml of 15% solution) over 3 to 5 minutes. If urine flow doesn't increase, second dose may be given; if response is inadequate after second dose, reevaluate patient.
➣ To prevent oliguria during cardiovascular and other surgeries
Adults: 50 to 100 g I.V. infusion as 5% to 15% solution
➣ Acute oliguria
Adults: Up to 100 g I.V. infusion as 15% to 25% solution
Children: 0.25 to 2 g/kg I.V. or 60 mg/m2 as 15% to 20% solution over 2 to 6 hours
➣ To reduce intracranial pressure and brain mass
Adults: 0.5 to 2 g/kg I.V. infusion as 15% to 25% solution given over 30 to 60 minutes
Children: 1 to 2 g/kg I.V. or 30 to 60 g/m2 over 30 to 60 minutes. Small or debilitated patients may require smaller dose of 500 mg/kg.
➣ To reduce intraocular pressure
Adults: 0.5 to 2 g/kg I.V. infusion as 15% to 25% solution given over 30 to 60 minutes. For preoperative use, give 60 to 90 minutes before surgery.
Children: 1 to 2 g/kg I.V. or 30 to 60 g/m2 over 30 to 60 minutes. Small or debilitated patients may require smaller dose of 500 mg/kg.
➣ To promote diuresis in drug toxicity
Adults: 5% to 25% solution by I.V. infusion given continuously to maintain high urine output
Children: 2 g/kg I.V. of 5% to 10% solution given continuously to maintain high urine output
➣ Irrigation during transurethral resection of prostate
Adults: 2.5% to 5% solution instilled into bladder via indwelling urethral catheter, as needed
Contraindications
• Active intracranial bleeding (except during craniotomy)
• Anuria secondary to severe renal disease
• Progressive heart failure, pulmonary congestion, renal damage, or renal dysfunction after mannitol therapy begins
• Severe pulmonary congestion or pulmonary edema
• Severe dehydration
Precautions
Use cautiously in:
• severe renal disease, heart failure, mild to moderate dehydration
• pregnant or breastfeeding patients.
Administration
☞ Withhold drug until adequate renal function and urinary output are established.
• When administering for drug toxicity, give fluids and electrolytes to match fluid loss.
• Be aware that at low temperatures, solution may crystallize (especially concentrations above 15%). If crystals form, warm bottle in hot-water bath or dry-heat oven or autoclave, then cool to body temperature or lower before giving.
• Don't give electrolyte-free mannitol solutions with blood; when giving blood with mannitol, add 20 mEq or more of sodium chloride solution to each liter of mannitol solution to avoid pseudoagglutination.
• Know that drug may be given as continuous or intermittent I.V. infusion. Infuse at prescribed rate using infusion device and in-line filter. Give single I.V. dose over 30 to 90 minutes in adults.
☞ Avoid extravasation, because it may cause local edema and tissue necrosis.
Adverse reactions
CNS: dizziness, headache, seizures
CV: chest pain, hypotension, hypertension, tachycardia, thrombophlebitis, heart failure, vascular overload
EENT: blurred vision, rhinitis
GI: nausea, vomiting, diarrhea, dry mouth
GU: polyuria, urinary retention, osmotic nephrosis
Metabolic: dehydration, water intoxication, hypernatremia, hyponatremia, hypovolemia, hypokalemia, hyperkalemia, metabolic acidosis
Respiratory: pulmonary congestion
Skin: rash, urticaria
Other: chills, fever, thirst, edema, extravasation with edema and tissue necrosis
Interactions
Drug-drug. Digoxin: increased risk of digoxin toxicity
Diuretics: increased therapeutic effects of mannitol
Lithium: increased urinary excretion of lithium
Drug-diagnostic tests. Electrolytes: increased or decreased levels
Patient monitoring
☞ Monitor I.V. site carefully to avoid extravasation and tissue necrosis.
• In comatose patient, insert indwelling urinary catheter as ordered to monitor urine output.
• Monitor renal function tests, urinary output, fluid balance, central venous pressure, and electrolyte levels (especially sodium and potassium).
☞ Watch for excessive fluid loss and signs and symptoms of hypovolemia and dehydration.
☞ Assess for evidence of circulatory overload, including pulmonary edema, water intoxication, and heart failure.
Patient teaching
• Teach patient about importance of monitoring exact urinary output.
☞ Advise patient to report pain at infusion site as well as adverse reactions, such as increased shortness of breath or pain in back, legs, or chest.
• Tell patient drug may cause thirst or dry mouth. Emphasize that fluid restrictions are necessary, but that frequent mouth care should ease these symptoms.
• As appropriate, review all other significant and life-threatening adverse reactions and interactions, especially those related to the drugs and tests mentioned above.
mannitol
(măn′ĭ-tôl′, -tōl′, -tŏl′)mannitol
A hexahydric sugar alcohol, which is used clinically as an osmotic diuretic to reduce brain swelling and intracranial pressure and to manage oliguric renal failure. It is also used to prime heart-lung pumps, to increase hydration of the upper airways in patients with cystic fibrosis and bronchiectasis, for acute glaucoma in veterinary medicine, and as a laxative.mannitol
A sugar sometimes given by injection as a concentrated solution to draw water from the brain in cases of ENCEPHALITIS or head injury. The drug is on the WHO official list.hyperosmotic agent
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