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Mannitol

Steven Tenny; Roshan Patel; William Thorell.

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Last Update: November 21, 2021.

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Continuing Education Activity


Mannitol can be used for the reduction of intracranial pressure and brain mass, to reduce
intraocular pressure if this is not achievable by other means, to promote diuresis for acute renal
failure to prevent or treat the oliguric phase before irreversible damage, and to promote diuresis
to promote excretion of toxic substances, materials, and metabolites. There are also multiple uses
of mannitol that are not FDA-approved. This activity will highlight the mechanism of action,
adverse event profile, pharmacology, monitoring, and relevant interactions of mannitol, pertinent
for interprofessional team members in treating patients with conditions where it is of clinical
value.
Objectives:
 Identify the FDA-approved indications for mannitol.
 Explain the mechanism of action for mannitol for each of the four FDA-approved
indications.
 Review the adverse effects and contraindications for using mannitol.
 Summarize interprofessional team strategies for improving care coordination and
communication to advance mannitol and improve outcomes.
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Indications
Mannitol has four Food and Drug Administration (FDA)-approved uses.
1. Mannitol has approval for the reduction of intracranial pressure and brain mass.[1]
2. Mannitol is approved to reduce intraocular pressure if this is not achievable by other
means.[2]
3. Mannitol can promote diuresis for acute renal failure to prevent or treat the oliguric phase
before irreversible damage.[3] 
4. Mannitol can also promote diuresis to promote the excretion of toxic substances,
materials, and metabolites.[4]
 There are multiple uses of mannitol that are not FDA-approved. 
 Mannitol may be used to prime a heart and lung machine before putting the patient on a
heart-lung bypass. The mannitol may help to preserve renal function as the kidneys have
decreased blood flow.  The mannitol is suspected to decrease renal cell swelling. 
 Mannitol works to protect sharp objects as they get introduced into a vascular space. A
mannitol cap on a pacemaker wire will protect the tip from becoming dulled while a
clinician introduces it into the vascular system then the mannitol will readily dissolve
away with minimal effect.
 Mannitol may have utility as a challenge test for diagnosing asthma.[5]
 Mannitol is a sweetener for diabetic food products. Mannitol is sugar but increases blood
glucose to a lesser extent than some other sugars such as sucrose.
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Mechanism of Action
Mannitol is a six-carbon, linear, simple sugar that is only mildly metabolized by the body and
primarily excreted rapidly by the kidneys when given intravenously and poorly absorbed when
taken orally. 
The FDA-approved indications for mannitol are all for intravenous mannitol and are
detailed below.
Mannitol for Increased Intracranial Pressure
Mannitol may be used for the reduction of intracranial pressure. In this indication, mannitol
administration is intravenous. Mannitol then constitutes a new solute in the plasma, which
increases the tonicity of the plasma. Since mannitol cannot cross the intact blood-brain barrier,
the increased tonicity from the manni
tol draws water out of the brain parenchyma and into the intravascular space. The water then
travels with the mannitol to the kidneys, where it gets excreted in the urine.[4]
The mannitol causes the cells in the brain to dehydrate mildly. The water inside the brain cells
(intracellular water) leaves the cells and enters the bloodstream as the mannitol draws it out of
the cells and into the bloodstream. Once in the bloodstream, the extra water is whisked out of the
skull.  When the mannitol gets to the kidneys, the kidneys filter the mannitol into the urine. The
mannitol again draws the water with it, and diuresis (increased urination) ensues.
Mannitol to Reduce Intraocular Pressure
Mannitol may be used to reduce intraocular pressure when given intravenously. The mannitol is
a new solute in the intravascular space, which increases the tonicity of the blood plasma. The
increased tonicity of the blood plasma draws water out of the vitreous humor of the eye and into
the intravascular space. Once in the intravascular space, the mannitol and associated water are
excreted by the kidney. The decreased water of the vitreous humor lowers the intraocular
pressure.[6]
The mannitol dehydrates the vitreous humor. The mannitol draws water out of the vitreous
humor and into the blood vessels as it passes by. When the vitreous humor has less water, after
being dehydrated by the mannitol, it has less mass and thus creates less pressure. The lower
pressure is less likely to damage the retina. The mannitol remains in the blood vessels and is
excreted in the urine with its associated water.
Mannitol to Promote Diuresis in Acute Renal Failure
Mannitol can be used in acute renal failure to help prevent or treat the oliguric phase. During the
oliguric phase, urine output decreases to less than 0.5 mg/kg/hour for children and less than 400
mL/day for adults. The fluid which does not get excreted remains in the body and causes fluid
overload. Fluid overload causes issues such as decreased oxygenation and ventilation, electrolyte
abnormalities, swelling, encephalopathy, and cardiac arrest. An individual with acute renal
failure can sometimes be given intravenous mannitol. Even during acute renal failure, much of
mannitol excretion is done by the kidneys. As the mannitol gets excreted, it draws water with it,
increasing the water excretion of the patient and helping avoid or treat the fluid overload caused
by oliguria in acute renal failure. However, mannitol causes significant osmotic injury to tubules
leading to ATN(acute tubular necrosis), so its use for this indication is almost obsolete.
Mannitol to Excrete Toxic Materials
Much like mannitol given for oliguria of acute renal failure, mannitol can be given to increase
the excretion of toxic materials, substances, and drugs. The kidneys excrete mannitol, which is
poorly reabsorbed once excreted and thus draws extra water with it into the renal collecting
ducts. The excess water in the renal collecting ducts can help increase the excretion of water-
soluble toxic materials, substances, and drugs.
Mannitol to Prevent Intradialytic Hypotension
Intradialytic hypotension and dialysis disequilibrium symptoms are common in hemodialysis
patients.  This is due to a drop in intradialytic osmolality. Mannitol can be used to prevent
intradialytic hypotension by raising serum osmolality.[7]
Additional Mechanisms of Action
Since mannitol is a sugar and it provides a sweet taste when ingested orally. Mannitol also
mostly passes through the intestine and is excreted in the feces as the small intestine absorbs it
poorly. Thus, mannitol is used as a sweetener in food for diabetic patients as mannitol can
provide sweetness to the food without increasing the blood sugar as much as sucrose.
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Administration
When using mannitol for medical purposes, it is given intravenously. Mannitol can be found in
varying concentrations from 5% mannitol (5 gm mannitol dissolved in 100 mL of fluid) up to
25% mannitol (25 gm of mannitol dissolved in 100 mL of fluid). A
commonly encountered solution is 20% mannitol (20 grams of mannitol dissolved in 100 mL of
fluid).[2]
 For increased intracranial pressure, dosages typically range from 0.25 g/kg to 2 g/kg
administered intravenously over 30 to 60 minutes with effect within 5 to 10 minutes and
lasting up to approximately 6 hours.
 For increased intraocular pressure, dosages typically range from 0.25 g/kg to 2 g/kg
administered intravenously over 30 to 60 minutes with effect within 5 to 10 minutes and
lasting up to approximately 6 hours.
 For prevention or treatment of oliguria, a test dose should be strongly considered of
around 0.2 g/kg intravenous to ensure a response to urine output. The mannitol infusion
can be adjusted to provide a urine flow rate of at least 30 mL/hour to 50 mL/hour in
adults.
 For excretion of toxic materials, the clinician may consider a dose of 0.25 g/kg to 2 g/kg
to observe its effects. If the patient receives more than 200 gm of mannitol without
benefit, mannitol use should be discontinued.
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Adverse Effects
There are multiple adverse effects that mannitol can cause, including:
 Masking or worsening dehydration as it causes diuresis
 Precipitate heart failure due to the rapid fluid shifts as water enters the intravascular
compartment
 Cause or worsen electrolyte abnormalities due to the shift of free water into the
intravascular space. Electrolyte abnormalities may include but are not limited to
hyponatremia, hypokalemia, and hypocalcemia.[8]
 Precipitate into crystals at low temperatures, which can cause vascular and end-organ
damage
 Worsen cerebral edema. Although mannitol poorly crosses the vessel wall, it does cross
to some degree, and mannitol more easily crosses injured vessels such as patients with
intracranial hemorrhage. Frequent doses of mannitol can cause mannitol to leach across
the blood-brain barrier and worsen cerebral edema as the mannitol, which has leached
into the brain, draws water into instead of out of the brain. Patients, especially children
with cerebral hyperemia, may have worsening cerebral edema with mannitol
administration.[8]
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Contraindications
There are multiple contraindications to giving mannitol, including:
 Established anuria due to renal disease
 Pulmonary edema or severe pulmonary congestion
 Active intracranial bleeding except for during a current craniotomy
 Severe dehydration
 Progressive heart failure
 Known mannitol hypersensitivity
 Renal damage caused by mannitol
 Patients with impaired renal function: If the patient has impaired renal function, a small
test dose should be given, and the patient observed for a response. If there is no response,
a small test dose is repeatable, but the clinician should administer no more than two test
doses.[9]
 Electrolyte abnormalities. As mannitol works, it first increases the intravascular free
water content, which can worsen electrolyte abnormalities, including hyponatremia. In
the second phase of action, mannitol gets excreted in the urine with excess free water,
potentially causing hypernatremia due to the induced diuresis. Electrolytes should be
monitored carefully with mannitol use.[9]
 Mannitol may worsen intracranial hypertension in patients, especially children with
hyperemia, which can be fatal.
 Repeated frequent doses of mannitol can leach into the brain and worsen cerebral edema
in the long term. Thus, mannitol is frequently recommended as a bolus spaced apart every
6 to 8 hours, limiting the number of boluses given.
 Mannitol can worsen renal function and precipitate renal failure.[10]
 Mannitol should only be given intravenously and never given intramuscularly or
subcutaneously.
 Mannitol should not be administered with whole blood.
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Monitoring
When giving mannitol, it is essential to monitor cardiac function as the fluid shifts can
precipitate heart failure. Additional electrolytes, including sodium, potassium, and osmolality, all
require monitoring. The clinician should stop mannitol if significant electrolyte abnormalities
develop or the osmolality reaches 320 mOsm or higher. Finally, urine output also requires
monitoring; failure for urine output to increase after administration of mannitol should prompt
cessation of mannitol and evaluation for possible renal or genitourinary issues.[9]
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Toxicity
Dialysis partially removes mannitol. Repeated doses of mannitol lead to the build-up of mannitol
even with dialysis.[11]
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Enhancing Healthcare Team Outcomes


An interprofessional team approach is an optimal approach with mannitol administration. It is
essential to monitor cardiac function as the fluid shifts can precipitate heart failure. Additional
electrolytes, including sodium, potassium, and osmolality, require monitoring by the nurses and
physicians. Abnormalities in these laboratory values necessitate prompt communication to all
members of the team. Mannitol administration should stop if significant electrolyte abnormalities
develop or the osmolality reaches 320 mOsm or higher. When mannitol is used to treat cerebral
edema, serum osmolality should be checked every 4 to 6 hours. If serum osmolality is more than
320 mOsm, alternative agents like the hypertonic solution should be used.
The nursing staff should pay particular attention to urine output and monitor it carefully,
reporting any concerns to the treating clinician. The pharmacist can verify dosing and perform
medication reconciliation and alert the team if any interactions are present. They can also
collaborate with the treating physician regarding potential alternative therapies in the event of
therapeutic failure or intolerance of mannitol. With open interprofessional communication
between all healthcare team members, any treatment, including mannitol, has the best chance at
optimal results. [Level 5]
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Review Questions
 Access free multiple choice questions on this topic.
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References
1.
Mesghali E, Fitter S, Bahjri K, Moussavi K. Safety of Peripheral Line Administration of
3% Hypertonic Saline and Mannitol in the Emergency Department. J Emerg Med. 2019
Apr;56(4):431-436. [PubMed]
2.
Alnemari AM, Krafcik BM, Mansour TR, Gaudin D. A Comparison of Pharmacologic
Therapeutic Agents Used for the Reduction of Intracranial Pressure After Traumatic
Brain Injury. World Neurosurg. 2017 Oct;106:509-528. [PubMed]
3.
Pasarikovski CR, Alotaibi NM, Al-Mufti F, Macdonald RL. Hypertonic Saline for
Increased Intracranial Pressure After Aneurysmal Subarachnoid Hemorrhage: A
Systematic Review. World Neurosurg. 2017 Sep;105:1-6. [PubMed]
4.
Wakai A, McCabe A, Roberts I, Schierhout G. Mannitol for acute traumatic brain
injury. Cochrane Database Syst Rev. 2013 Aug 05;(8):CD001049. [PMC free article]
[PubMed]
5.
Sverrild A, Leadbetter J, Porsbjerg C. The use of the mannitol test as an outcome
measure in asthma intervention studies: a review and practical recommendations. Respir
Res. 2021 Nov 07;22(1):287. [PMC free article] [PubMed]
6.
Weber AC, Blandford AD, Costin BR, Perry JD. Effect of mannitol on globe and orbital
volumes in humans. Eur J Ophthalmol. 2018 Mar;28(2):163-167. [PubMed]
7.
Mc Causland FR, Prior LM, Heher E, Waikar SS. Preservation of blood pressure stability
with hypertonic mannitol during hemodialysis initiation. Am J Nephrol. 2012;36(2):168-
74. [PMC free article] [PubMed]
8.
Rossi S, Picetti E, Zoerle T, Carbonara M, Zanier ER, Stocchetti N. Fluid Management in
Acute Brain Injury. Curr Neurol Neurosci Rep. 2018 Sep 11;18(11):74. [PubMed]
9.
Koenig MA. Cerebral Edema and Elevated Intracranial Pressure. Continuum (Minneap
Minn). 2018 Dec;24(6):1588-1602. [PubMed]
10.
Karajala V, Mansour W, Kellum JA. Diuretics in acute kidney injury. Minerva
Anestesiol. 2009 May;75(5):251-7. [PubMed]
11.
Boulanger EF, Sabag-Daigle A, Thirugnanasambantham P, Gopalan V, Ahmer BMM.
Sugar-Phosphate Toxicities. Microbiol Mol Biol Rev. 2021 Dec
15;85(4):e0012321. [PMC free article] [PubMed]

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