Pronunciation:
(MAN i tole)
U.S. Brand Names:
Osmitrol®; Resectisol®
Synonyms:
D-Mannitol
Generic Available:
Yes
Canadian Brand Names:
Osmitrol®
Use:
Reduction of increased intracranial pressure associated with cerebral edema; promotion of diuresis in the prevention and/or treatment of oliguria or anuria due to acute renal failure; reduction of increased intraocular pressure; promoting urinary excretion of toxic substances; genitourinary irrigant in transurethral prostatic resection or other transurethral surgical procedures
Pregnancy Risk Factor:
C
Lactation:
Excretion in breast milk unknown
Contraindications:
Hypersensitivity to mannitol or any component or the formulation; severe renal disease (anuria); dehydration; active intracranial bleeding; severe pulmonary edema or congestion
Warnings/Precautions:
Should not be administered until adequacy of renal function and urine flow is established; cardiovascular status should also be evaluated; do not administer electrolyte-free mannitol solutions with blood
Adverse Reactions:
Frequency not defined.
Cardiovascular: Circulatory overload, CHF
Central nervous system: Headache, convulsions, headache, chills, dizziness
Dermatologic: Rash
Endocrine & metabolic: Fluid and electrolyte imbalance, water intoxication, dehydration and hypovolemia secondary to rapid diuresis, hyponatremia
Gastrointestinal: Nausea, vomiting, xerostomia
Genitourinary: Polyuria, dysuria
Local: Tissue necrosis
Ocular: Blurred vision
Respiratory: Pulmonary edema
Miscellaneous: Allergic reactions
Overdosage/Toxicology:
Symptoms of overdose include polyuria, hypotension, cardiovascular collapse, pulmonary edema, hyponatremia, hypokalemia, oliguria, and seizures. Increased electrolyte excretion and fluid overload can occur. Hemodialysis will clear mannitol and reduce osmolality.
Drug Interactions:
Lithium toxicity (with diuretic-induced hyponatremia)
Stability:
Should be stored at room temperature (15°C to 30°C) and protected from freezing; crystallization may occur at low temperatures; do not use solutions that contain crystals, heating in a hot water bath and vigorous shaking may be utilized for resolubilization; cool solutions to body temperature before using
Compatibility:
Y-site administration: Compatible: Allopurinol, amifostine, amphotericin B cholesteryl sulfate complex, aztreonam, cisatracurium, cladribine, docetaxel, etoposide, fludarabine, fluorouracil, gatifloxacin, gemcitabine, idarubicin, linezolid, melphalan, ondansetron, paclitaxel, piperacillin/tazobactam, propofol, remifentanil, sargramostim, teniposide, thiotepa, vinorelbine. Incompatible: Cefepime, doxorubicin liposome, filgrastim
Compatibility when admixed: Compatible: Amikacin, bretylium, cefamandole, cefoxitin, cimetidine, cisplatin, dopamine, fosphenytoin, furosemide, gentamicin, metoclopramide, nizatidine, ofloxacin, ondansetron, sodium bicarbonate, tobramycin, verapamil. Incompatible: Imipenem/cilastatin, meropenem. Variable (consult detailed reference): Etoposide with cisplatin and potassium chloride, potassium chloride
Mechanism of Action:
Increases the osmotic pressure of glomerular filtrate, which inhibits tubular reabsorption of water and electrolytes and increases urinary output
Pharmacodynamics/Kinetics:
Onset of action: Diuresis: Injection: 1-3 hours; Reduction in intracerebral pressure: ~15 minutes
Duration: Reduction in intracerebral pressure: 3-6 hours
Distribution: Remains confined to extracellular space (except in extreme concentrations); does not penetrate the blood-brain barrier
Metabolism: Minimally hepatic to glycogen
Half-life elimination: 1.1-1.6 hours
Excretion: Primarily urine (as unchanged drug)
Dosage:
I.V.:
Children:
Test dose (to assess adequate renal function): 200 mg/kg over 3-5 minutes to produce a urine flow of at least 1 mL/kg for 1-3 hours
Initial: 0.5-1 g/kg
Maintenance: 0.25-0.5 g/kg given every 4-6 hours
Adults:
Test dose (to assess adequate renal function): 12.5 g (200 mg/kg) over 3-5 minutes to produce a urine flow of at least 30-50 mL of urine per hour over the next 2-3 hours
Initial: 0.5-1 g/kg
Maintenance: 0.25-0.5 g/kg every 4-6 hours; usual adult dose: 20-200 g/24 hours
Intracranial pressure: Cerebral edema: 1.5-2 g/kg/dose I.V. as a 15% to 20% solution over 30 minutes; maintain serum osmolality 310-320 mOsm/kg
Preoperative for neurosurgery: 1.5-2 g/kg administered 1-1.5 hours prior to surgery
Transurethral irrigation: Use urogenital solution as required for irrigation
Administration:
In-line 5-micron filter set should always be used for mannitol infusion with concentrations 20%; administer test dose (for oliguria) I.V. push over 3-5 minutes; avoid extravasation; for cerebral edema or elevated ICP, administer over 20-30 minutes; crenation and agglutination of red blood cells may occur if administered with whole blood
Monitoring Parameters:
Renal function, daily fluid I & O, serum electrolytes, serum and urine osmolality; for treatment of elevated intracranial pressure, maintain serum osmolality 310-320 mOsm/kg
Patient Education:
This medication can only be given by infusion. Report immediately any muscle weakness, numbness, tingling, acute headache, nausea, dizziness, blurred vision, eye pain, respiratory difficulty, chest pain, or pain at infusion site. Pregnancy/breast-feeding precautions: Inform prescriber if you are pregnant. Consult prescriber if breast-feeding.
Additional Information:
May autoclave or heat to redissolve crystals; mannitol 20% has an approximate osmolarity of 1100 mOsm/L and mannitol 25% has an approximate osmolarity of 1375 mOsm/L
Anesthesia and Critical Care Concerns/Other Considerations:
Mannitol may autoclave or heat to redissolve crystals.
Mannitol 20% has an approximate osmolarity of 1100 mOsm/L.
Mannitol 25% has an approximate osmolarity of 1375 mOsm/L.
Dental Health: Effects on Dental Treatment:
No significant effects or complications reported
Dental Health: Vasoconstrictor/Local Anesthetic Precautions:
No information available to require special precautions
Mental Health: Effects on Mental Status:
May cause dizziness
Mental Health: Effects on Psychiatric Treatment:
Has been used to treat lithium toxicity/overdose but its overall effect in lowering serum lithium level is minimum; if toxicity is severe, hemodialysis is the treatment of choice
Dosage Forms:
Injection, solution: 5% [50 mg/mL] (1000 mL); 10% [100 mg/mL] (500 mL, 1000 mL); 15% [150 mg/mL] (500 mL); 20% [200 mg/mL] (150 mL, 250 mL, 500 mL); 25% [250 mg/mL] (50 mL)
Osmitrol®: 5% [50 mg/mL] (1000 mL); 10% [100 mg/mL] (500 mL, 1000 mL); 15% [150 mg/mL] (500 mL); 20% [200 mg/mL] (250 mL, 500 mL)
Solution, urogenital (Resectisol®): 5% [50 mg/mL] (2000 mL, 4000 mL)
International Brand Names:
Apir Manitol® (ES); Intramed Mannitol Infusion® (ZA); Isotol® (IT); Manit® (HR, SI); Manitol Baxter® (ES); Manitol® (ID, RO); Manitol Mein® (ES); Manitol Vitulia® (ES); Maniton® (TH); Mannisol A® (HU); Mannisol B® (HU); Mannistol® (IT); Mannite Saprochi® (CH); Mannit Fresenius® (AT); Mannit Mayrhofer® (AT); Mannitol ANB® (TH); Mannitol Baxter® (DK, LU); Mannitol Baxter Kalbe® (ID); Mannitol Baxter Viaflo® (SE); Mannitol B.Braun® (CH, FI); Mannitol® (BG, GB, IN, NO, PL, RO, TR, YU); Mannitol Bichsel® (CH); Mannitol Bieffe® (HU); Mannitol Chi Sheng® (TH); Mannitol Fresenius Kabi® (DK, SE); Mannitolo® (IT); Mannitol SAD® (DK); Mannitol Thai Otsuka® (TH); Mannitol Vioser® (RO); Mede-Prep® (AU); Osmitrol® (CA); Osmofundina® (ES); Osmofundin-N® (LU); Osmorin® (EC); Osmosteril® (LU); Resectisol® (TR); Soluciones Parenterales® (AR, CL)
References
Al-Sarraf M, Fletcher W, Oishi N, et al, "Cisplatin Hydration With and Without Mannitol Diuresis in Refractory Disseminated Malignant Melanoma: A Southwest Oncology Group Study,"Cancer Treat Rep, 1982, 66(1):31-5.
Gadallah MF, Lynn M, and Work J, "Case Report: Mannitol Nephrotoxicity Syndrome: Role of Hemodialysis and Postulate of Mechanisms,"Am J Med Sci, 1995, 309(4):219-22.
Goodwin WE and Latta H, "Focal Osmotic Nephrosis Due to Therapeutic Use of Mannitol: A Case of Perirenal Hematoma After Renal Biopsy,"J Urol, 1970, 103(1):11-4.
Holdener EE, Park CH, Belt RJ, et al, "Effect of Mannitol and Plasma on the Cytotoxicity of Cisplatin,"Eur J Cancer Clin Oncol, 1983, 19(4):515-8.
Huff JS, "Acute Mannitol Intoxication in a Patient With Normal Renal Function,"Am J Emerg Med, 1990, 8(4):338-9.
Jahns BE, Avula S, Lipscomb JW, et al, "Mannitol for Severe Ciguatera Intoxication,"J Toxicol Clin Toxicol, 1995, 33(5):496.
Moses FM, "Colonic Perforation Due to Oral Mannitol,"JAMA, 1988, 260(5):640.
Ostrow S, Egorin MJ, Hahn D, et al, "High-Dose Cisplatin Therapy Using Mannitol Versus Furosemide Diuresis: Comparative Pharmacokinetics and Toxicity,"Cancer Treat Rep, 1981, 65(1-2):73-8.
Palmquist KL, Quattrocchi FP, and Looney LA, "Compatibility of Furosemide With 20% Mannitol,"Am J Health Syst Pharm, 1995, 52(6):648,50.
Shapiro WR and Shapiro JR, "Principles of Brain Tumor Chemotherapy,"Semin Oncol, 1986, 13(1):56-69.