Compound
D-mannitol
A diuretic and renal diagnostic aid related to sorbitol. It has little significant energy value as it is largely eliminated from the body before any metabolism can take place. It can be used to treat oliguria associated with kidney failure or other manifestations of inadequate renal function and has been used for determination of glomerular filtration rate. Mannitol is also commonly used as a research tool in cell biological studies, usually to control osmolarity.
Structure
Loading the model…
- Class
- Organic compound
- Formula
- C6H14O6
- Mass
- 182.172 g/mol
- Charge
- 0
- InChIKey
- FBPFZTCFMRRESA-KVTDHHQDSA-N
- SMILES
- OC[C@@H](O)[C@@H](O)[C@H](O)[C@H](O)CO
- Look it up
- ChEBIPubChemBy InChIKey
Identity from ChEBI, geometry from PubChem. Not evidence.
What it touches on the way
Mechanistic reach
1 entity
1 entities reached.
0 reported hops1 assembled from the scaffold
What the reference databases state
Statements
9 statements
9 statements · 1 reference database · Subject: D-mannitol · Sources: Rhea
- D-mannitol is converted to D-fructoseCompoundRhea RHEA:16765Inferred only
- D-mannitol is converted to D-fructoseCompoundRhea RHEA:12084Inferred only
- D-fructose is converted to D-mannitolCompoundRhea RHEA:12084Inferred only
- D-fructose is converted to D-mannitolCompoundRhea RHEA:16765Inferred only
- D-mannose is converted to D-mannitolCompoundRhea RHEA:18513Inferred only
- D-mannose is converted to D-mannitolCompoundRhea RHEA:15029Inferred only
- D-mannitol is converted to D-mannoseCompoundRhea RHEA:18513Inferred only
- D-mannitol is converted to D-mannoseCompoundRhea RHEA:15029Inferred only
- D-mannitol is transported by AQP9ProteinRhea RHEA:81355Inferred only
Reactions
9 reactions
D-mannitol+NAD(1-)D-fructose+NADH(2-)+hydron
Reaction pageDirection not assertedBalanced
Rhea RHEA:12084CC BY 4.0Reference data
D-mannitol+NAD(1-)D-mannose+NADH(2-)+hydron
Reaction pageDirection not assertedBalanced
Rhea RHEA:15029CC BY 4.0Reference data
D-mannitol+NADP(3-)D-fructose+NADPH(4-)+hydron
Reaction pageDirection not assertedBalanced
Rhea RHEA:16765CC BY 4.0Reference data
D-mannitol+2Fe(III)-[cytochrome c]D-fructose+2Fe(II)-[cytochrome c]+2hydron
Reaction pageDirection not assertedBalance undeterminable
Rhea RHEA:17597CC BY 4.0Reference data
D-mannitol+dioxygenD-mannose+hydrogen peroxide
Reaction pageDirection not assertedBalanced
Rhea RHEA:18513CC BY 4.0Reference data
CHEBI:61381+waterD-mannitol+hydrogenphosphate
Reaction pageDirection not assertedBalanced
Rhea RHEA:19537CC BY 4.0Reference data
D-mannitol+N(pros)-phospho-L-histidyl-[protein]CHEBI:61381+L-histidyl-[protein]
Reaction pageDirection not assertedBalance undeterminable
Rhea RHEA:33363CC BY 4.0Reference data
Transported by AQP9
Reaction pageDirection not assertedBalanced
Rhea RHEA:81355CC BY 4.0Reference data
CHEBI:231796+D-mannitolCHEBI:206556+diphosphate(3-)
Reaction pageDirection not assertedBalanced
Rhea RHEA:82587CC BY 4.0Reference data
On the label
Labelled products
20 products
Source: NIH DSLD · Ingredient: D-mannitol · 20 products · Declared amount per serving: 0.3–3 Gram(s) (10 products)
18 labels state an amount2 do not
- BulkSupplements.comMannitol3 Gram(s)per 3 Gram(s)DSLD:252699
- BulkSupplements.comMannitol3 Gram(s)per 3 Gram(s)DSLD:253990
- BulkSupplements.comMannitol3 Gram(s)per 3 Gram(s)DSLD:253992
- BulkSupplements.comMannitol3 Gram(s)per 3 Gram(s)DSLD:253993
- BulkSupplements.comMannitol3 Gram(s)per 3 Gram(s)DSLD:311029
- BulkSupplements.comMannitol3 Gram(s)per 3 Gram(s)DSLD:311030
- BulkSupplements.comMannitol3 Gram(s)per 3 Gram(s)DSLD:311031
- BulkSupplements.comMannitol3 Gram(s)per 3 Gram(s)DSLD:311032
- Health Products DistributorsRejuvenate! Plusamount not statedper 31.2 Gram(s)DSLD:254933
- Herbs SRADiuret+16 mgper 2 Capsule(s)DSLD:316145
- MetagenicsOxygenics25 mgper 1 Tablet(s)DSLD:27676
- MetagenicsOxygenics25 mgper 1 Tablet(s)DSLD:27677
Show the remaining 8
- PerqueActivated B-12 Guard295 mgper 1 Lozenge(s)DSLD:240619
- PerqueActivated B-12 Guard Lozenges295 mgper 1 Lozenge(s)DSLD:18693
- PerqueLife Guard Chewables200 mgper 1 Chewable Tablet(s)DSLD:240860
- PerqueVessel Health Guard181 mgper 1 Lozenge(s)DSLD:241007
- PerqueZinc & Throat Guard Lozenges200 mgper 1 Lozenge(s)DSLD:241012
- TwinlabMega B-12 Dots 5000 mcgamount not statedper 1 Microlozenge(s)DSLD:17850
- Z Natural FoodsCordyceps Mushroom Extract0.3 Gram(s)per 2.8 Gram(s)DSLD:299847
- Z Natural FoodsCordyceps Mushroom Extract Powder0.3 Gram(s)per 2.8 Gram(s)DSLD:299848
Label record: NIH Office of Dietary Supplements · CC0
Registered, and not reported
- Source
- ClinicalTrials.gov
- Intervention
- D-mannitol
- Status
- Completed, terminated or suspended
- Results posted
- No
Trials without posted results
277 trials
277 registered trials without posted results · Overdue (FDAAA 801): 104 · Showing 120 of 277
104 past the window16 within it, or no actual date
- NCT01386710suspended— PI left previous institution study will reopen at new institution.expected 2027-12a university or hospital
- NCT04386070suspended— Lack of IMP availability - may resume.expected 2026-12-31a university or hospital
- NCT03895567suspended— The study was suspended while the researchers secured new funding.expected 2026-12a university or hospital
- NCT03105843completed2026-07-31a university or hospital
- NCT07605260completed2026-06-30a university or hospital
- NCT07090824completed2026-05-29a university or hospital
- NCT06884514completed2026-05-13a university or hospital
- NCT06905652completed2026-05-12a university or hospital
- NCT07675356completed2026-04-30a university or hospital
- NCT05962606completed2026-03-16industry
- NCT05902819completed2026-03-02a university or hospital
- NCT07089329completed2026-02-25a university or hospital
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- NCT02148796completed2026-01-30a university or hospital
- NCT06644534completed2026-01-12industry
- NCT07064720completed2025-12-22a university or hospital
- NCT06414330completed2025-11-12a university or hospital
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- NCT05277636completed2024-01-13a university or hospitalpast the reporting window
- NCT05034367completed2023-12-31a university or hospitalpast the reporting window
- NCT05979727terminated— The trial was closed due to futility2023-12-10industrypast the reporting window
- NCT06681415completed2023-12-01a university or hospitalpast the reporting window
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- NCT04293744terminated— Slow recruitment2023-08-31industrypast the reporting window
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- NCT04227756completed2022-09-02a university or hospitalpast the reporting window
- NCT04140773terminated— Poor participant recruitment2022-08-31a university or hospitalpast the reporting window
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- NCT05199142terminated— Development plan changed2022-03-11industrypast the reporting window
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- NCT04321850terminated— Health restrictions due to the COVID-19 pandemic2020-06-30a government bodypast the reporting window
- NCT02728687completed2020-03-30a university or hospitalpast the reporting window
- NCT03545997terminated— lack of recruitment2020-03-20a university or hospitalpast the reporting window
- NCT04468854terminated— Corona-Virus Lockdown (16th March in Switzerland)2020-03-15a university or hospitalpast the reporting window
- NCT03620422completed2020-01-31a university or hospitalpast the reporting window
- NCT04205045completed2020-01-24a university or hospitalpast the reporting window
- NCT04094168completed2019-12-15a university or hospitalpast the reporting window
- NCT03573999completed2019-10-31a university or hospitalpast the reporting window
- NCT04004923completed2019-10-25a university or hospitalpast the reporting window
- NCT04188353completed2019-08-24a university or hospitalpast the reporting window
- NCT01858922completed2019-08-12a university or hospitalpast the reporting window
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- NCT06773429completed2019-07-31a university or hospitalpast the reporting window
- NCT03321136completed2019-07-05a university or hospitalpast the reporting window
- NCT02991781completed2019-06a university or hospitalpast the reporting window
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- NCT03639727completed2018-12-31a university or hospitalpast the reporting window
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- NCT03933787completed2018-07-18a university or hospitalpast the reporting window
- NCT02603822completed2018-07-17a university or hospitalpast the reporting window
Where it reaches
3 systems, 3 regions, 7 tissues, 7 transporter routes — routes, not measurements: transporters known to carry D-mannitol are expressed there, and no source reports it arriving.
Loading the model…
Papers screened
640 papers
- Compound
- D-mannitol
- Screened
- 640
- Admitted
- 0
- Discarded
- 250
- Not read
- 390
- Showing
- 200 of 640
Discarded: the wrong intervention152 papers
- PMID:10695605cited by PMID:20395849; not about the subject it would be filed under2026-10-13
- PMID:10926839cited by PMID:20395849; not about the subject it would be filed under2026-10-13
- PMID:11251042cited by PMID:20395849; not about the subject it would be filed under2026-10-13
- PMID:11804845cited by PMID:20395849; not about the subject it would be filed under2026-10-13
- PMID:1181664cited by PMID:20395849; not about the subject it would be filed under2026-10-13
- PMID:12409280cited by PMID:20395849; not about the subject it would be filed under2026-10-13
- PMID:12899695cited by PMID:20395849; not about the subject it would be filed under2026-10-13
- PMID:1310242cited by PMID:20395849; not about the subject it would be filed under2026-10-13
- PMID:15479938cited by PMID:20395849; not about the subject it would be filed under2026-10-13
- PMID:15601832cited by PMID:20395849; not about the subject it would be filed under2026-10-13
- PMID:15851691cited by PMID:20395849; not about the subject it would be filed under2026-10-13
- PMID:1616036cited by PMID:20395849; not about the subject it would be filed under2026-10-13
and 140 more.
Discarded: another reason, stated per paper26 papers
- PMID:3084067no claim extracted — subject_absent — DOSED: Paper is about macrophage-induced thioguanine resistance (HGPRT loss) in mouse mammary tumor cells; mannitol is never mentioned in the abstract | Macrophage coculture inducing thioguanine-resistant variants in mouse mammary tumor cells; the abstract never mentions mannitol2026-10-12
and 25 more.
Discarded: no comparator24 papers
and 24 more.
Discarded: no extractable result22 papers
- PMID:20395849claims extracted but the two passes did not agree2026-10-12
- PMID:925708no claim extracted — no_quantitative_result2026-10-12
and 20 more.
Discarded: an endpoint this vocabulary does not hold16 papers
- PMID:10727667no claim extracted — no_outcome_node — measured: NF-kappaB reporter activity in cultured vascular smooth muscle cells, cis-reporter plasmid | NF-kappaB cis-reporter activity in cultured vascular smooth muscle cells2026-10-12
- PMID:1117429no claim extracted — no_outcome_node — measured: net water transport across everted hamster jejunal segments in vitro | net water absorption in everted hamster jejunal sacs, in vitro2026-10-12
- PMID:19628223no claim extracted — no_outcome_node — measured: renal perfusion pressure in isolated perfused rat kidney, constant pressure mode | renal perfusion pressure in an isolated perfused rat kidney, constant-pressure perfusion2026-10-12
- PMID:22023943no claim extracted — vocabulary gap, passes disagreed: no_outcome_node / endpoint_near_miss — measured: kidney tissue oxidative stress markers (MDA, MPO, SOD, reduced glutathione) and histopathological acute renal injury score in rat ischemia/reperfusion | kidney tissue malondialdehyde, biochemical assay of harvested kidneys (the node is circulating MDA in plasma, serum or whole blood)2026-10-12
and 12 more.
Discarded: not retrievable10 papers
- PMID:4949350no PMID parsed, abstract under 200 characters, or no record returned by efetch2026-10-13
- PMID:8832789no PMID parsed, abstract under 200 characters, or no record returned by efetch2026-10-13
- PMID:9388700no PMID parsed, abstract under 200 characters, or no record returned by efetch2026-10-13
- PMID:6038078no PMID parsed, abstract under 200 characters, or no record returned by efetch2026-10-07
- PMID:6401883no PMID parsed, abstract under 200 characters, or no record returned by efetch2026-10-07
and 5 more.
Not read yet390 papers
- PMID:100700582026-10-13
- PMID:21166772026-10-13
- PMID:109192832026-10-08
- PMID:105856312026-10-06
- PMID:89307582026-10-06
- PMID:114307072026-10-05
- PMID:124962272026-10-05
- PMID:172295352026-10-05
- PMID:108156792026-09-29
- PMID:124226252026-09-29
- PMID:125152912026-09-29
- PMID:126917962026-09-29
and 378 more.
Measured, not recorded
- Compound
- D-mannitol
- Endpoints measured
- 253 endpoints
- Recorded as a finding
- No
Show what was measured
Glutathione (GSH) level after 48 h
decreases
A 48-h incubation with high glucose substantially reduced glutathione (GSH) levels compared with normoglycemic VSMCs
PMID:10727667 · one of two readings recorded this
Glutathione (GSH) level after 48 h
increases
whereas mannitol significantly increased GSH levels
PMID:10727667 · one of two readings recorded this
NF-kappaB activity (reporter), acute
increases
Within 3-h incubation, high glucose (27.5 or 55 mmol/l) alone induced an increase in NF-kappaB activity in VSMCs
PMID:10727667 · one of two readings recorded this
NF-kappaB activity (reporter), acute
increases
this increase was mimicked by mannitol given to deliver the same osmolar stress to the cells
PMID:10727667 · one of two readings recorded this
TNFalpha-induced NF-kappaB activation
decreases
An antioxidant N-acetyl-L-cysteine and a selective protein kinase C (PKC) inhibitor GF109203X significantly suppressed the TNFalpha-induced NF-kappaB activation
PMID:10727667 · one of two readings recorded this
TNFalpha-stimulated NF-kappaB activation after 48 h
increases
Incubation with high glucose for 48 h followed by stimulation with TNFalpha led to a marked potentiation of NF-kappaB activation compared with normoglycemic (5.5 mmol/l) VSMCs exposed to TNFalpha
PMID:10727667 · one of two readings recorded this
TNFalpha-stimulated NF-kappaB activation after 48 h
decreases
while mannitol attenuated this effect
PMID:10727667 · one of two readings recorded this
TNFalpha-stimulated NF-kappaB activity, acute
increases
High glucose or mannitol also enhanced TNFalpha-stimulated NF-kappaB activity
PMID:10727667 · one of two readings recorded this
all-cause mortality (death)
RR for death = 0.83; 95% CI 0.47 to 1.46 (ICP-directed therapy vs standard care)
One trial compared ICP-directed therapy to 'standard care' (RR for death= 0.83; 95% CI 0.47;1.46).
PMID:10796744 · one of two readings recorded this
all-cause mortality, ICP-directed therapy versus standard care
RR for death= 0.83; 95% CI 0.47-1.46
One trial compared ICP-directed therapy to 'standard care' (RR for death= 0.83; 95% CI 0.47;1.46).
PMID:10796744 · one of two readings recorded this
all-cause mortality, mannitol versus other ICP-lowering agents
No trials compared mannitol to other ICP lowering agents.
PMID:10796744 · one of two readings recorded this
all-cause mortality, mannitol versus pentobarbital and other approaches to intracranial-pressure-lowering therapy after acute traumatic brain injury
RR for death = 0.85; 95% CI 0.52-1.38, mannitol versus pentobarbital
Not recorded as a finding: the comparison was against another active treatment
One trial compared mannitol to pentobarbital (RR for death = 0.85; 95% CI 0. 52;1.38).
PMID:10796744 · one of two readings recorded this
all-cause mortality, mannitol versus pentobarbital
RR for death = 0.85; 95% CI 0.52-1.38
One trial compared mannitol to pentobarbital (RR for death = 0.85; 95% CI 0. 52;1.38).
PMID:10796744 · one of two readings recorded this
all-cause mortality, pre-hospital mannitol versus placebo
RR for death=1.59; 95% CI 0.44-5.79
One trial tested the effectiveness of pre-hospital administration of mannitol against placebo (RR for death=1.59; 95% CI 0.44;5.79).
PMID:10796744 · one of two readings recorded this
intracranial pressure control (guideline recommendation on mannitol use, not a discrete quantitative endpoint)
decreases
Not recorded as a finding: a design this vocabulary does not classify
Mannitol is effective in reducing ICP, and its use is recommended as a guideline in the management of traumatic intracranial hypertension.
PMID:10937895 · one of two readings recorded this
intracranial pressure (ICP) control / effectiveness of mannitol, guideline recommendation without primary trial data reported
decreases
Not recorded as a finding: a design this vocabulary does not classify
Mannitol is effective in reducing ICP, and its use is recommended as a guideline in the management of traumatic intracranial hypertension.
PMID:10937895 · one of two readings recorded this
case fatality, dependency, and side effects after acute stroke
Case fatality, the proportion of dependent patients, and side effects were not reported and were not available from the investigators.
PMID:11062300 · one of two readings recorded this
case fatality, proportion of dependent patients, and side effects after acute ischemic stroke or cerebral parenchymal hemorrhage treated with mannitol
Not recorded as a finding: no estimate is reported anywhere
As a result of lack of appropriate randomized trials, currently no conclusion can be drawn on the effects of mannitol in acute stroke.
PMID:11062300 · one of two readings recorded this
contractile rate, ileum (dogs)
decreases
decreases in the ileum occurred primarily by a decrease in contractile rate
PMID:1117429 · one of two readings recorded this
force per contraction, antrum (dogs)
decreases
antral decreases could be attributed primarily to a decrease in force per contraction
PMID:1117429 · one of two readings recorded this
net water absorption (everted hamster jejunum)
decreases
Magnesium sulfate, like mannitol, only reduced net water absorption when present as a component of a hypertonic mucosal solution
PMID:1117429 · one of two readings recorded this
net water absorption (everted hamster jejunum)
decreases
Magnesium sulfate, like mannitol, only reduced net water absorption when present as a component of a hypertonic mucosal solution
PMID:1117429 · one of two readings recorded this
net water and electrolyte absorption in everted segments of hamster jejunum, in vitro, isotonic versus hypertonic mannitol
decreases
Not recorded as a finding: this platform holds no node for the endpoint
Magnesium sulfate, like mannitol, only reduced net water absorption when present as a component of a hypertonic mucosal solution.
PMID:1117429 · one of two readings recorded this
net water transport (everted hamster jejunum)
decreases, p = 0.01
Sodium ricinoleate (2.0 mM) reduced net water transport by 48 percent (P smaller than .01)
PMID:1117429 · one of two readings recorded this
proximal colonic activity (dogs)
decreases
Proximal colonic activity tended to decrease after laxatives and feeding
PMID:1117429 · one of two readings recorded this
total contractile activity, antrum and ileum (dogs)
decreases
Decreases in total activity were found for both cathartics in the antrum and ileum
PMID:1117429 · one of two readings recorded this
case fatality and dependency after acute ischaemic stroke or cerebral parenchymal haemorrhage, mannitol versus placebo or open control
Not recorded as a finding: no estimate is reported anywhere
Neither beneficial nor harmful effects of mannitol could be proved.
PMID:11279707 · one of two readings recorded this
case fatality and dependency after acute ischaemic stroke or cerebral parenchymal haemorrhage
n = 77
The number of included patients was small (36 treated and 41 controls) and the follow up was short.
PMID:11279707 · one of two readings recorded this
case fatality and dependency after acute stroke
n = 77
Neither beneficial nor harmful effects of mannitol could be proved.
PMID:11279707 · one of two readings recorded this
short and long-term case fatality and dependency after acute ischaemic stroke or cerebral parenchymal haemorrhage
n = 77
Not recorded as a finding: no estimate is reported anywhere
The number of included patients was small (36 treated and 41 controls) and the follow up was short.
PMID:11279707 · one of two readings recorded this
all-cause mortality and death-or-severe-disability, high-dose versus conventional-dose mannitol, in patients with acute intracranial haemorrhage managed pre-operatively
decreases, RR = 0.55; 95% CI 0.36-0.84 for mortality and RR = 0.58; 95% CI 0.45-0.74 for death or severe disability, high-dose versus conventional-dose mannitol
Not recorded as a finding: the comparison was against another active treatment
In the pre-operative management of patients with acute intracranial haemorrhage the administration of high-dose mannitol resulted in reduced mortality (RR=0.55; 95%CI 0.36, 0.84) and reduced death and severe disability (RR=0.58; 95%CI 0.45, 0.74) when compared with conventional-dose mannitol.
PMID:12804397 · one of two readings recorded this
all-cause mortality (death)
decreases, RR = 0.55; 95% CI 0.36 to 0.84 (high-dose vs conventional-dose mannitol)
In the pre-operative management of patients with acute intracranial haemorrhage the administration of high-dose mannitol resulted in reduced mortality (RR=0.55; 95%CI 0.36, 0.84) and reduced death and severe disability (RR=0.58; 95%CI 0.45, 0.74) when compared with conventional-dose mannitol.
PMID:12804397 · one of two readings recorded this
all-cause mortality, high-dose versus conventional-dose mannitol
decreases, RR = 0.55; 95% CI 0.36-0.84
In the pre-operative management of patients with acute intracranial haemorrhage the administration of high-dose mannitol resulted in reduced mortality (RR=0.55; 95%CI 0.36, 0.84) and reduced death and severe disability (RR=0.58; 95%CI 0.45, 0.74) when compared with conventional-dose mannitol.
PMID:12804397 · one of two readings recorded this
all-cause mortality, ICP-directed therapy versus standard care
RR for death= 0.83; 95%CI 0.47-1.46
One trial compared ICP-directed therapy to 'standard care' (RR for death= 0.83; 95%CI 0.47,1.46).
PMID:12804397 · one of two readings recorded this
all-cause mortality, mannitol versus other ICP-lowering agents
No trials compared mannitol to other ICP-lowering agents.
PMID:12804397 · one of two readings recorded this
all-cause mortality, mannitol versus pentobarbital
RR for death = 0.85; 95% CI 0.52-1.38
One trial compared mannitol to pentobarbital (RR for death = 0.85; 95% CI 0.52, 1.38).
PMID:12804397 · one of two readings recorded this
all-cause mortality, pre-hospital mannitol versus placebo
RR for death=1.75; 95% CI 0.48-6.38
One trial tested the effectiveness of pre-hospital administration of mannitol against placebo (RR for death=1.75; 95% CI 0.48, 6.38).
PMID:12804397 · one of two readings recorded this
death and severe disability composite
decreases, RR = 0.58; 95% CI 0.45 to 0.74 (high-dose vs conventional-dose mannitol)
In the pre-operative management of patients with acute intracranial haemorrhage the administration of high-dose mannitol resulted in reduced mortality (RR=0.55; 95%CI 0.36, 0.84) and reduced death and severe disability (RR=0.58; 95%CI 0.45, 0.74) when compared with conventional-dose mannitol.
PMID:12804397 · one of two readings recorded this
death or severe disability, high-dose versus conventional-dose mannitol
decreases, RR = 0.58; 95% CI 0.45-0.74
In the pre-operative management of patients with acute intracranial haemorrhage the administration of high-dose mannitol resulted in reduced mortality (RR=0.55; 95%CI 0.36, 0.84) and reduced death and severe disability (RR=0.58; 95%CI 0.45, 0.74) when compared with conventional-dose mannitol.
PMID:12804397 · one of two readings recorded this
case fatality and treatment outcomes in children and adults with cerebral malaria given mannitol or urea as adjunct therapy
Not recorded as a finding: no estimate is reported anywhere
We identified no randomized or quasi-randomized controlled trials to support or refute the use of mannitol or urea as adjuncts for treating cerebral malaria in clinical practice.
PMID:15495121 · one of two readings recorded this
case fatality / treatment outcomes with mannitol or urea adjunct therapy for cerebral malaria
We identified no randomized or quasi-randomized controlled trials to support or refute the use of mannitol or urea as adjuncts for treating cerebral malaria in clinical practice.
PMID:15495121 · one of two readings recorded this
clinical outcome of treating cerebral malaria with mannitol or urea as adjunct therapy
No trials met the inclusion criteria.
PMID:15495121 · one of two readings recorded this
all-cause mortality, ICP-directed therapy versus standard care
RR for death= 0.83; 95% CI 0.47-1.46
One trial compared ICP-directed therapy to 'standard care' (RR for death= 0.83; 95% CI 0.47 to 1.46).
PMID:16235278 · one of two readings recorded this
all-cause mortality, mannitol versus hypertonic saline
RR for death= 1.25; 95% CI 0.47-3.33
One trial compared mannitol to hypertonic saline (RR for death= 1.25; 95% CI 0.47 to 3.33).
PMID:16235278 · one of two readings recorded this
all-cause mortality, mannitol versus pentobarbital
RR for death= 0.85; 95% CI 0.52-1.38
One trial compared mannitol to pentobarbital (RR for death= 0.85; 95% CI 0.52 to 1.38).
PMID:16235278 · one of two readings recorded this
all-cause mortality, pre-hospital mannitol versus placebo
RR for death= 1.75; 95% CI 0.48-6.38
One trial tested the effectiveness of pre-hospital administration of mannitol against placebo (RR for death= 1.75; 95% CI 0.48 to 6.38).
PMID:16235278 · one of two readings recorded this
all-cause mortality (death)
RR for death = 0.85; 95% CI 0.52 to 1.38 (mannitol vs pentobarbital)
One trial compared mannitol to pentobarbital (RR for death = 0.85; 95% CI 0.52 to 1.38).
PMID:17253453 · one of two readings recorded this
all-cause mortality following different mannitol therapy regimens, mannitol compared with other intracranial-pressure-lowering agents, and mannitol given at different times after acute traumatic brain injury
RR for death = 0.85; 95% CI 0.52-1.38, mannitol versus pentobarbital
Not recorded as a finding: the comparison was against another active treatment
One trial compared mannitol to pentobarbital (RR for death = 0.85; 95% CI 0.52 to 1.38).
PMID:17253453 · one of two readings recorded this
all-cause mortality, ICP-directed therapy versus standard care
RR for death = 0.83; 95% CI 0.47-1.46
One trial compared ICP-directed therapy to 'standard care' (RR for death = 0.83; 95% CI 0.47 to 1.46).
PMID:17253453 · one of two readings recorded this
all-cause mortality, mannitol versus hypertonic saline
RR for death = 1.25; 95% CI 0.47-3.33
One trial compared mannitol to hypertonic saline (RR for death = 1.25; 95% CI 0.47 to 3.33).
PMID:17253453 · one of two readings recorded this
all-cause mortality, mannitol versus pentobarbital
RR for death = 0.85; 95% CI 0.52-1.38
One trial compared mannitol to pentobarbital (RR for death = 0.85; 95% CI 0.52 to 1.38).
PMID:17253453 · one of two readings recorded this
all-cause mortality, pre-hospital mannitol versus placebo
RR for death = 1.75; 95% CI 0.48-6.38
One trial tested the effectiveness of pre-hospital administration of mannitol against placebo (RR for death = 1.75; 95% CI 0.48 to 6.38).
PMID:17253453 · one of two readings recorded this
case fatality (death) and functional worsening/dependency in acute ischaemic stroke and intracerebral haemorrhage, individual trial comparisons narrated rather than pooled
no effect
Not recorded as a finding: a review that discusses its trials without pooling them
Case fatality did not differ between the mannitol and control groups in the ICH trials.
PMID:17636655 · one of two readings recorded this
case fatality (death), mannitol vs control, in intracerebral haemorrhage trials
no effect
Not recorded as a finding: a review that discusses its trials without pooling them
Case fatality did not differ between the mannitol and control groups in the ICH trials.
PMID:17636655 · one of two readings recorded this
change in intracranial pressure (delta ICP) as a function of mannitol dose, meta-regression across dose-response studies
delta ICP = 6.6 x dose - 1.1, weak linear relationship, R2 = 0.05, p = 0.27
Not recorded as a finding: this platform holds no node for the endpoint
Meta-regression found a weak linear relationship between change in ICP (delta ICP) and dose (delta ICP = 6.6 x dose - 1.1; p = 0.27, R(2) = 0.05).
PMID:18173314 · one of two readings recorded this
intracranial pressure change (delta ICP) in relation to mannitol dose, meta-regression across 18 studies
delta ICP = 6.6 x dose - 1.1; p = 0.27, R(2) = 0.05, p = 0.27
Not recorded as a finding: this platform holds no node for the endpoint
Meta-regression found a weak linear relationship between change in ICP (delta ICP) and dose (delta ICP = 6.6 x dose - 1.1; p = 0.27, R(2) = 0.05).
PMID:18173314 · one of two readings recorded this
contrast-induced nephropathy, defined as a 0.5-mg/dL absolute or 25% relative increase in creatinine within 48 hours of coronary angiography
increases, Contrast-induced nephropathy occurred in 23 (50%) intervention patients versus 13 (28%) controls (relative risk, 1.77; 95% confidence interval, 1.03 to 3.05; P = 0.03; adjusted odds ratio, 3.73; P = 0.03)., p = 0.03, n = 92
Not recorded as a finding: the intervention held more than the compound
Contrast-induced nephropathy occurred in 23 (50%) intervention patients versus 13 (28%) controls (relative risk, 1.77; 95% confidence interval, 1.03 to 3.05; P = 0.03; adjusted odds ratio, 3.73; P = 0.03).
PMID:19535188 · one of two readings recorded this
contrast-induced nephropathy incidence, defined by a rise in serum creatinine of at least 0.5 mg/dL or 25%, within 48 hours of coronary angiography
increases, relative risk 1.77 (95% CI 1.03 to 3.05), P = 0.03; adjusted odds ratio 3.73, P = 0.03, p = 0.03, n = 92
Not recorded as a finding: the intervention held more than the compound
Contrast-induced nephropathy occurred in 23 (50%) intervention patients versus 13 (28%) controls (relative risk, 1.77; 95% confidence interval, 1.03 to 3.05; P = 0.03; adjusted odds ratio, 3.73; P = 0.03).
PMID:19535188 · one of two readings recorded this
Pancreas and renal perfusion pressure
increases
Pancreas and renal perfusion pressures increased by >50% in the ischemia group immediately upon reperfusion
PMID:19628223 · one of two readings recorded this
Perfusion pressure
no effect
Conversely, perfusion pressure in the treatment group was not significantly different from the control
PMID:19628223 · one of two readings recorded this
Reduced glutathione level and xanthine oxidase
increases
The reduced glutathione level increased significantly, as did XO, immediately upon starting reperfusion in both organs appertaining to the ischemic group
PMID:19628223 · one of two readings recorded this
Urine output
decreases
Urine output was severely reduced in the IR kidneys
PMID:19628223 · one of two readings recorded this
alpha-gustducin mRNA regional variation
modulates, p = 0.006
as did α-gustducin (P = 0.006, peaking in midsmall bowel)
PMID:20395849 · one of two readings recorded this
GLUT2 mRNA and total cell protein
no effect, p = 0.17
This response was specific to SGLT1, with no measured change in the levels of facilitated glucose transporter GLUT2 mRNA or total cell protein (P ≥ 0.17, Fig. 1B)
PMID:20395849 · one of two readings recorded this
SGLT1 expression after D-glucose infusion
unclear, p = 0.093
however, the increase did not reach significance, indicating that the response is more modest in the distal segments (2.2 ± 0.5-fold up-regulation, P = 0.093 vs. water, P = 0.35 vs. glucose)
PMID:20395849 · one of two readings recorded this
SGLT1 expression after D-glucose infusion
increases, p = 0.012
with a 2.7 ± 0.4-fold up-regulation in SGLT1 expression (P = 0.012 compared with whole intestinal infusion of water, P = 0.76 compared with whole intestinal infusion of glucose)
PMID:20395849 · one of two readings recorded this
SGLT1 expression after D-glucose infusion
increases, p = 0.0029
Infusion of proximal jejunum gave similar results, with 2.9 ± 0.2-fold up-regulation of SGLT1 (P = 0.0029 vs. water, P = 0.94 vs. glucose)
PMID:20395849 · one of two readings recorded this
SGLT1 mRNA
no effect, p = 0.29
This was mediated by post-transcriptional mechanisms as there was no observed change in mRNA signal (0.85 ± 0.1-fold change, P = 0.29, Fig. 1A)
PMID:20395849 · one of two readings recorded this
SGLT1 protein signal in rat jejunal mucosa after 3-hour intestinal infusion, Western blot densitometry
no effect, indistinguishable from water infusion, p = 0.63
Not recorded as a finding: this platform holds no node for the endpoint
Mannitol infusion yielded an SGLT1 protein signal indistinguishable from water infusion (P = 0.63, Fig. 1C).
PMID:20395849 · one of two readings recorded this
SGLT1 protein
increases, p = 0.0035
Infusion of 250 mM D-fructose led to an up-regulation of SGLT1 protein similar to D-glucose, with a 2.3 ± 0.2-fold increase in SGLT1 expression after 3-hour (: P = 0.0035 vs. water; P = 0.42 vs. D-glucose)
PMID:20395849 · one of two readings recorded this
SGLT1 protein
no effect, p = 0.63
Mannitol infusion yielded an SGLT1 protein signal indistinguishable from water infusion (P = 0.63, Fig. 1C)
PMID:20395849 · one of two readings recorded this
SGLT1 response to D-glucose infusion
no effect, p = 0.98
De-afferentation of the vagus entirely blocked the response to D-glucose infusion (1.0 ± 0.2-fold change, P = 0.98)
PMID:20395849 · one of two readings recorded this
SGLT1 response to D-glucose infusion
no effect, p = 0.14
with D-glucose infusion in the presence of ondansetron inducing a nonsignificant 1.8± 0.4-fold increase in SGLT1 (P = 0.14) compared with water infusion under the same conditions
PMID:20395849 · one of two readings recorded this
SGLT1 total cellular protein
increases, p = 0.013
Infusion of the intestine with D-glucose for 3 hours during normal fasting periods led to a rapid up-regulation of total cellular SGLT1 (2.9 ± 0.6-fold increase, P = 0.013) compared with infusion of water alone
PMID:20395849 · one of two readings recorded this
SGLT1 whole cell protein
increases, p = 0.003
Infusion of 0.3% saccharin induced a 2.2 ± 0.2-fold increase in SGLT1 whole cell protein expression (: P = 0.003 vs. water; P = 0.29 vs. D-glucose)
PMID:20395849 · one of two readings recorded this
T1R2 mRNA regional variation
no effect, p = 0.081
T1R2 was also predominantly expressed in the proximal bowel, although this variation in expression topography did not reach significance (P = 0.081)
PMID:20395849 · one of two readings recorded this
T1R3 mRNA regional variation
modulates, p = 0.034
T1R3 showed a clear regional variation, peaking in proximal jejunum (P = 0.0340, Kruskal-Wallis ANOVA)
PMID:20395849 · one of two readings recorded this
mannitol crystallization yield from fermentation broth
180 g l(-1) crystallized
Not recorded as a finding: a review that discusses its trials without pooling them
Mannitol at 180 g l(-1) can be crystallized out from the fermentation broth by cooling crystallization.
PMID:21063702 · one of two readings recorded this
mannitol production yield from fermentation broth
180 g l(-1) crystallized
Mannitol at 180 g l(-1) can be crystallized out from the fermentation broth by cooling crystallization.
PMID:21063702 · one of two readings recorded this
onset of acute oliguric renal failure
developed within 3.5 +/- 1.1 days, n = 8
In the present series, acute oliguric renal failure developed within 3.5 +/- 1.1 (mean +/- SD) days after receiving daily and total mannitol doses of 189 +/- 64 g and 626 +/- 270 g, respectively, over 3.5 +/- 1.5 days.
PMID:2111870 · one of two readings recorded this
peak serum creatinine in patients with mannitol-induced acute renal failure
5.7 +/- 2.7 mg/dl
Not recorded as a finding: the paper never states the instrument the node requires
The peak serum creatinine was 5.7 +/- 2.7 mg/dl and peak osmolal gap was 74 +/- 39 mOsm/kg water.
PMID:2111870 · one of two readings recorded this
peak serum creatinine
5.7 +/- 2.7 mg/dl
The peak serum creatinine was 5.7 +/- 2.7 mg/dl and peak osmolal gap was 74 +/- 39 mOsm/kg water.
PMID:2111870 · one of two readings recorded this
major neurological sequelae in children surviving cerebral malaria
no effect
Not recorded as a finding: no outcome node exists for neurological sequelae of cerebral malaria
No difference in mortality, time to regain consciousness, or neurological sequelae were detected.
PMID:21491391 · one of two readings recorded this
mortality, time to regain consciousness, and neurological sequelae, mannitol 20% vs saline placebo, in children with cerebral malaria
no effect, n = 156
Not recorded as a finding: the supporting sentence never names the compound
No difference in mortality, time to regain consciousness, or neurological sequelae were detected.
PMID:21491391 · one of two readings recorded this
time to regain consciousness in children with cerebral malaria
no effect
Not recorded as a finding: no outcome node exists for recovery-of-consciousness time
No difference in mortality, time to regain consciousness, or neurological sequelae were detected.
PMID:21491391 · one of two readings recorded this
sensitivity and specificity of mannitol challenge versus standard exercise challenge testing for diagnosing exercise-induced bronchoconstriction
sensitivity ranged 58-96%, specificity ranged 65-78%
In the 3 diagnostic cross-sectional studies that evaluated mannitol, the sensitivity and specificity ranged from 58 to 96% and 65 to 78%, respectively.
PMID:21875541 · one of two readings recorded this
sensitivity and specificity of the mannitol challenge test for diagnosing exercise-induced bronchoconstriction, against standard exercise challenge testing
sensitivity 58%-96%, specificity 65%-78%
In the 3 diagnostic cross-sectional studies that evaluated mannitol, the sensitivity and specificity ranged from 58 to 96% and 65 to 78%, respectively.
PMID:21875541 · one of two readings recorded this
ARI score (tubular necrosis and acute inflammation)
decreases, p = 0.043
whereas phlebotomy or/and mannitol treatments significantly decreased tubular necrosis and inflammatory infiltration (p values for group [I/R] versus group [P], [M], and [P + M] were 0.043, 0.043, and 0.003, respectively)
PMID:22023943 · one of two readings recorded this
ARI score (tubular necrosis and acute inflammation)
decreases, p = 0.003
whereas phlebotomy or/and mannitol treatments significantly decreased tubular necrosis and inflammatory infiltration (p values for group [I/R] versus group [P], [M], and [P + M] were 0.043, 0.043, and 0.003, respectively)
PMID:22023943 · one of two readings recorded this
ARI score (tubular necrosis and acute inflammation)
decreases, p = 0.043
whereas phlebotomy or/and mannitol treatments significantly decreased tubular necrosis and inflammatory infiltration (p values for group [I/R] versus group [P], [M], and [P + M] were 0.043, 0.043, and 0.003, respectively)
PMID:22023943 · one of two readings recorded this
ARI score (tubular necrosis and acute inflammation)
increases, p = 0.012
Histological evaluation of ARI score showed that aortic I/R significantly increased (p value for group [S] versus group [I/R] was 0.012)
PMID:22023943 · one of two readings recorded this
Kidney MDA level
increases, p = 0.05
Aortic I/R significantly increased the level of MDA (reflecting lipid peroxidation), SOD (enzymatic endogenous antioxidant), and MPO (reflecting neutrophil infiltration) activity (p < 0.05)
PMID:22023943 · one of two readings recorded this
Kidney MDA level
decreases, p = 0.05
Phlebotomy or/and mannitol treatments significantly decreased the level of MDA, SOD, and MPO activity and increased glutathione level (nonenzymatic antioxidant in the kidney tissues) (p < 0.05)
PMID:22023943 · one of two readings recorded this
Kidney MPO activity
increases, p = 0.05
Aortic I/R significantly increased the level of MDA (reflecting lipid peroxidation), SOD (enzymatic endogenous antioxidant), and MPO (reflecting neutrophil infiltration) activity (p < 0.05)
PMID:22023943 · one of two readings recorded this
Kidney MPO activity
decreases, p = 0.05
Phlebotomy or/and mannitol treatments significantly decreased the level of MDA, SOD, and MPO activity and increased glutathione level (nonenzymatic antioxidant in the kidney tissues) (p < 0.05)
PMID:22023943 · one of two readings recorded this
Kidney reduced glutathione level
increases, p = 0.05
Phlebotomy or/and mannitol treatments significantly decreased the level of MDA, SOD, and MPO activity and increased glutathione level (nonenzymatic antioxidant in the kidney tissues) (p < 0.05)
PMID:22023943 · one of two readings recorded this
Kidney SOD activity
increases, p = 0.05
Aortic I/R significantly increased the level of MDA (reflecting lipid peroxidation), SOD (enzymatic endogenous antioxidant), and MPO (reflecting neutrophil infiltration) activity (p < 0.05)
PMID:22023943 · one of two readings recorded this
Kidney SOD activity
decreases, p = 0.05
Phlebotomy or/and mannitol treatments significantly decreased the level of MDA, SOD, and MPO activity and increased glutathione level (nonenzymatic antioxidant in the kidney tissues) (p < 0.05)
PMID:22023943 · one of two readings recorded this
kidney tissue malondialdehyde, superoxide dismutase and myeloperoxidase activity, reduced glutathione, and histological ARI score after lower-limb ischaemia/reperfusion in rats
decreases
Not recorded as a finding: a node exists but the paper states a different instrument or population
Phlebotomy or/and mannitol treatments significantly decreased the level of MDA, SOD, and MPO activity and increased glutathione level (nonenzymatic antioxidant in the kidney tissues) (p < 0.05).
PMID:22023943 · one of two readings recorded this
differences between hydration regimens after iopromide
no effect
After iopromide, the differences between the hydration regimens were much less, as iopromide increased urine flow rates much more than iodixanol
PMID:22353855 · one of two readings recorded this
glomerular filtration rate and urine viscosity in rats after contrast medium
Not recorded as a finding: the intervention held more than the compound
By virtue of its stronger diuretic effect, the Mannit-Gluc regimen greatly diminished the increase in urine viscosity and completely prevented the transient decrease in GFR caused by iodixanol with the NaCl regimen.
PMID:22353855 · one of two readings recorded this
increase in urine viscosity after iodixanol
decreases
By virtue of its stronger diuretic effect, the Mannit-Gluc regimen greatly diminished the increase in urine viscosity
PMID:22353855 · one of two readings recorded this
transient decrease in GFR after iodixanol
decreases
completely prevented the transient decrease in GFR caused by iodixanol with the NaCl regimen
PMID:22353855 · one of two readings recorded this
urine flow rate
increases
The Mannit-Gluc regimen resulted in higher urine flow rates than the standard NaCl regimen, yet maintained a good volume status
PMID:22353855 · one of two readings recorded this
intracranial pressure reduction (mm Hg), mannitol versus hypertonic sodium solutions in traumatic brain injury
The weighted mean difference in ICP reduction, using hypertonic sodium solutions compared with mannitol, was 1.39 mm Hg (95% CI -0.74 to 3.53).
Not recorded as a finding: the comparison was against another active treatment
The weighted mean difference in ICP reduction, using hypertonic sodium solutions compared with mannitol, was 1.39 mm Hg (95% CI -0.74 to 3.53).
PMID:23811861 · one of two readings recorded this
pooled mean reduction in intracranial pressure (ICP) by weighted mean difference, mannitol vs hypertonic sodium solutions in traumatic brain injury
weighted mean difference in ICP reduction, hypertonic sodium solutions vs mannitol, 1.39 mm Hg (95% CI -0.74 to 3.53), n = 171
Not recorded as a finding: the comparison was against another active treatment
The weighted mean difference in ICP reduction, using hypertonic sodium solutions compared with mannitol, was 1.39 mm Hg (95% CI -0.74 to 3.53).
PMID:23811861 · one of two readings recorded this
all-cause mortality (RR for death), pre-hospital administration of mannitol versus placebo trial
RR for death = 1.75; 95% CI 0.48 to 6.38
Not recorded as a finding: the paper never states the instrument the node requires
One trial tested the effectiveness of pre-hospital administration of mannitol against placebo (RR for death = 1.75; 95% CI 0.48 to 6.38).
PMID:23918314 · one of two readings recorded this
death (all-cause mortality) by relative risk, mannitol vs pentobarbital, in acute traumatic brain injury
RR for death = 0.85 (95% CI 0.52 to 1.38), mannitol vs pentobarbital
Not recorded as a finding: the comparison was against another active treatment
One trial compared mannitol to pentobarbital (RR for death = 0.85; 95% CI 0.52 to 1.38).
PMID:23918314 · one of two readings recorded this
anaphylactic/allergic reaction to mannitol
increases
We present a case report of a patient who experienced an anaphylactic response to mannitol and review the literature.
PMID:24060838 · one of two readings recorded this
anaphylactic hypersensitivity reaction to mannitol in a single patient, case report
increases, anaphylactic response occurred, n = 1
Not recorded as a finding: no estimate is reported anywhere
We present a case report of a patient who experienced an anaphylactic response to mannitol and review the literature.
PMID:24060838 · one of two readings recorded this
anaphylactic/hypersensitivity reaction to mannitol
increases, anaphylactic response occurred, n = 1
We present a case report of a patient who experienced an anaphylactic response to mannitol and review the literature.
PMID:24060838 · both readings recorded this
anaphylactic reaction to mannitol in a single patient (case report)
increases
Not recorded as a finding: this platform holds no node for the endpoint
We present a case report of a patient who experienced an anaphylactic response to mannitol and review the literature.
PMID:24060838 · one of two readings recorded this
Anaphylactic reaction
increases, n = 1
We present a case report of a patient who experienced an anaphylactic response to mannitol and review the literature.
PMID:24060838 · one of two readings recorded this
serum creatinine, overall pooled across all AKI-risk subgroups
no effect, MD 1.63, 95% CI -6.02 to 9.28
Not recorded as a finding: The sentence carrying the pooled null result does not name the compound or the outcome on its own ("Overall, there was no significant difference between the experimental group and control group") — both live in the preceding sentence ("Eight studies reported the outcome of SCr change"), so it is not self-supporting. Only the radiocontrast subgroup had a self-supporting sentence, and that was claimed instead.
Overall, there was no significant difference between the experimental group and control group (MD 1.63, 95% CI −6.02 to 9.28; I2 = 63%, P = 0.008).
PMID:24454783 · one of two readings recorded this
serum creatinine (SCr) change, overall
no effect, MD 1.63, 95% CI -6.02 to 9.28
Overall, there was no significant difference between the experimental group and control group (MD 1.63, 95% CI −6.02 to 9.28; I2 = 63%, P = 0.008).
PMID:24454783 · one of two readings recorded this
urinary volume change (ml/24h)
no effect, MD -140.56, 95% CI -650.05 to 368.93
Not recorded as a finding: No outcome node in the closed list covers urine output volume, and separately the sentence reporting this null result does not itself name mannitol (the subject lives in the preceding sentence, "Change of urinary volume can be extracted from five comparisons in four RCTs").
There was no difference in change of urine output (MD −140.56, 95% CI −650.05 to 368.93), but the heterogeneity was significant across studies (I2 = 71%, P = 0.008).
PMID:24454783 · one of two readings recorded this
urine output change (ml/24h)
no effect, MD -140.56, 95% CI -650.05 to 368.93
There was no difference in change of urine output (MD −140.56, 95% CI −650.05 to 368.93), but the heterogeneity was significant across studies (I2 = 71%, P = 0.008).
PMID:24454783 · one of two readings recorded this
acute renal failure (osmotic nephrosis)
Large doses/massive infusions of mannitol have been found to be associated with acute renal failure (MI-ARF), that is, osmotic nephrosis.
PMID:24941319 · one of two readings recorded this
intraoperative brain relaxation (brain bulge / tense brain)
increases, RR 0.60 (95% CI 0.44 to 0.83) favouring hypertonic saline
The risk ratio for brain bulge or tense brain in the hypertonic saline group was 0.60 (95% confidence interval (CI) 0.44 to 0.83, low-quality evidence).
PMID:25019296 · one of two readings recorded this
urinary lactulose:mannitol ratio (L:M), assessing intestinal permeability and absorption
The most commonly used test has been the urinary lactulose to mannitol ratio (L:M), which primarily assesses gut leakiness, and which also measures absorption.
PMID:25305289 · one of two readings recorded this
urinary lactulose to mannitol ratio (L:M), gut permeability and absorption
The most commonly used test has been the urinary lactulose to mannitol ratio (L:M), which primarily assesses gut leakiness, and which also measures absorption.
PMID:25305289 · one of two readings recorded this
all-cause mortality
n = 191
Studies were underpowered to detect a significant difference in mortality or neurological outcomes.
PMID:26825644 · both readings recorded this
all-cause mortality, neurological disability, ICP change from baseline, ICP treatment failure, and serious adverse events, pooled across randomised trials comparing hypertonic saline and mannitol in severe traumatic brain injury with elevated ICP
increases, risk ratio (RR) = 0.39; 95% CI 0.18-0.81 favoring hypertonic saline over mannitol for ICP treatment failure
Not recorded as a finding: the comparison was against another active treatment
No difference between HTS and mannitol was observed for mean ICP reduction; however, risk of ICP treatment failure favored HTS (risk ratio [RR] = 0.39; 95% CI = 0.18-0.81).
PMID:26825644 · one of two readings recorded this
ICP treatment failure
risk ratio [RR] = 0.39; 95% CI = 0.18-0.81, favoring hypertonic sodium solutions over mannitol
No difference between HTS and mannitol was observed for mean ICP reduction; however, risk of ICP treatment failure favored HTS (risk ratio [RR] = 0.39; 95% CI = 0.18-0.81).
PMID:26825644 · both readings recorded this
mean ICP reduction
no effect
No difference between HTS and mannitol was observed for mean ICP reduction; however, risk of ICP treatment failure favored HTS (risk ratio [RR] = 0.39; 95% CI = 0.18-0.81).
PMID:26825644 · one of two readings recorded this
mean intracranial pressure (ICP) reduction
no effect
No difference between HTS and mannitol was observed for mean ICP reduction; however, risk of ICP treatment failure favored HTS (risk ratio [RR] = 0.39; 95% CI = 0.18-0.81).
PMID:26825644 · one of two readings recorded this
globe and orbital volume by computed tomography before and after intravenous mannitol administration
decreases, globe volume decreased 186 mm3 (-2.5%) after mannitol administration, p = 0.02
Not recorded as a finding: this platform holds no node for the endpoint
Average globe volume decreased 186 mm3 (-2.5%, p = 0.02) after mannitol administration, while average orbital volume increased 353 mm3 (+3.5%, p = 0.04).
PMID:28777386 · one of two readings recorded this
globe and orbital volume by CT imaging before and after intravenous mannitol administration
decreases, -186 mm3 (-2.5%) globe volume, p = 0.02, n = 14
Not recorded as a finding: this platform holds no node for the endpoint
Average globe volume decreased 186 mm3 (-2.5%, p = 0.02) after mannitol administration, while average orbital volume increased 353 mm3 (+3.5%, p = 0.04).
PMID:28777386 · one of two readings recorded this
globe volume and orbital volume by CT imaging, before and after intravenous mannitol administration in neurosurgical ICU patients
decreases, -2.5% (globe volume), +3.5% (orbital volume), p = 0.02
Not recorded as a finding: the result compares a group with itself, not with a control
Average globe volume decreased 186 mm3 (-2.5%, p = 0.02) after mannitol administration, while average orbital volume increased 353 mm3 (+3.5%, p = 0.04).
PMID:28777386 · one of two readings recorded this
globe volume and orbital volume by CT imaging before and after intravenous mannitol administration
decreases, -186 mm3 (-2.5%) globe volume, p = 0.02
Not recorded as a finding: this platform holds no node for the endpoint
Average globe volume decreased 186 mm3 (-2.5%, p = 0.02) after mannitol administration, while average orbital volume increased 353 mm3 (+3.5%, p = 0.04).
PMID:28777386 · one of two readings recorded this
globe volume by CT imaging, before vs after intravenous mannitol
decreases, -186 mm3 (-2.5%), p = 0.02, n = 14
Average globe volume decreased 186 mm3 (-2.5%, p = 0.02) after mannitol administration, while average orbital volume increased 353 mm3 (+3.5%, p = 0.04).
PMID:28777386 · one of two readings recorded this
Globe volume by CT imaging
decreases, -2.5%, p = 0.02, n = 14
Average globe volume decreased 186 mm3 (-2.5%, p = 0.02) after mannitol administration, while average orbital volume increased 353 mm3 (+3.5%, p = 0.04).
PMID:28777386 · both readings recorded this
orbital volume by CT imaging, before vs after intravenous mannitol
increases, +353 mm3 (+3.5%), p = 0.04, n = 14
Average globe volume decreased 186 mm3 (-2.5%, p = 0.02) after mannitol administration, while average orbital volume increased 353 mm3 (+3.5%, p = 0.04).
PMID:28777386 · one of two readings recorded this
Orbital volume by CT imaging
increases, +3.5%, p = 0.04, n = 14
Average globe volume decreased 186 mm3 (-2.5%, p = 0.02) after mannitol administration, while average orbital volume increased 353 mm3 (+3.5%, p = 0.04).
PMID:28777386 · both readings recorded this
blood-brain barrier (BBB) permeability to gentamicin, guinea pig sampling
no effect, did not reach statistical significance, p = 0.581
Not recorded as a finding: no outcome node exists for barrier permeability to a co-administered drug
Mannitol increased the rate of entry and egress of gentamicin through BLB significantly (p = 0.0044) but the effects on the BBB did not reach statistical significance (p = 0.581).
PMID:29228990 · one of two readings recorded this
blood-brain barrier (BBB) permeability to gentamicin
no effect, did not reach statistical significance, p = 0.581
Mannitol increased the rate of entry and egress of gentamicin through BLB significantly (p = 0.0044) but the effects on the BBB did not reach statistical significance (p = 0.581).
PMID:29228990 · both readings recorded this
blood-brain barrier permeability to gentamicin
no effect, p = 0.581, p = 0.581
Not recorded as a finding: reports a permeability rate change, not a listed outcome node and not a named PK parameter eligible for exposure_claims
Mannitol increased the rate of entry and egress of gentamicin through BLB significantly (p = 0.0044) but the effects on the BBB did not reach statistical significance (p = 0.581).
PMID:29228990 · one of two readings recorded this
blood-labyrinth barrier (BLB) permeability to gentamicin, guinea pig perilymph/CSF sampling
increases, increased rate of entry and egress through BLB, p = 0.0044
Not recorded as a finding: no outcome node exists for barrier permeability to a co-administered drug
Mannitol increased the rate of entry and egress of gentamicin through BLB significantly (p = 0.0044) but the effects on the BBB did not reach statistical significance (p = 0.581).
PMID:29228990 · one of two readings recorded this
Blood-labyrinth barrier (BLB) permeability to gentamicin (rate of entry/egress)
increases, p = 0.0044
Mannitol increased the rate of entry and egress of gentamicin through BLB significantly (p = 0.0044) but the effects on the BBB did not reach statistical significance (p = 0.581).
PMID:29228990 · one of two readings recorded this
blood-labyrinth barrier (BLB) permeability to gentamicin
increases, increased rate of entry and egress through BLB, p = 0.0044
Mannitol increased the rate of entry and egress of gentamicin through BLB significantly (p = 0.0044) but the effects on the BBB did not reach statistical significance (p = 0.581).
PMID:29228990 · one of two readings recorded this
blood-labyrinth barrier permeability to gentamicin (rate of entry/egress)
increases, p = 0.0044, p = 0.0044
Not recorded as a finding: reports a permeability rate change, not a listed outcome node and not a named PK parameter (AUC/Cmax/clearance) eligible for exposure_claims
Mannitol increased the rate of entry and egress of gentamicin through BLB significantly (p = 0.0044) but the effects on the BBB did not reach statistical significance (p = 0.581).
PMID:29228990 · one of two readings recorded this
gentamicin blood-labyrinth barrier (BLB) and blood-brain barrier (BBB) permeability, rate of entry and egress
increases, p = 0.0044
Not recorded as a finding: two different barriers reported in one sentence with distinct significance levels; the cleaner renal-clearance finding (pk_parameter clearance) was recorded as the exposure claim from this paper, so this mixed two-barrier finding was set aside rather than force it into one pk_parameter/estimate pairing
Mannitol increased the rate of entry and egress of gentamicin through BLB significantly (p = 0.0044) but the effects on the BBB did not reach statistical significance (p = 0.581).
PMID:29228990 · one of two readings recorded this
permeability of the blood-brain barrier (BBB) to gentamicin
no effect, the effects on the BBB did not reach statistical significance, p = 0.581
Mannitol increased the rate of entry and egress of gentamicin through BLB significantly (p = 0.0044) but the effects on the BBB did not reach statistical significance (p = 0.581).
PMID:29228990 · one of two readings recorded this
permeability of the blood-labyrinth barrier (BLB) to gentamicin
increases, Mannitol increased the rate of entry and egress of gentamicin through BLB significantly, p = 0.0044
Mannitol increased the rate of entry and egress of gentamicin through BLB significantly (p = 0.0044) but the effects on the BBB did not reach statistical significance (p = 0.581).
PMID:29228990 · one of two readings recorded this
rate of entry and egress of gentamicin through the blood-brain barrier (BBB)
no effect, the effects on the BBB did not reach statistical significance, p = 0.581
Not recorded as a finding: no outcome/pk node exists for blood-brain barrier permeability; effect not statistically significant
Mannitol increased the rate of entry and egress of gentamicin through BLB significantly (p = 0.0044) but the effects on the BBB did not reach statistical significance (p = 0.581).
PMID:29228990 · one of two readings recorded this
rate of entry and egress of gentamicin through the blood-labyrinth barrier (BLB)
increases, Mannitol increased the rate of entry and egress of gentamicin through BLB significantly, p = 0.0044
Not recorded as a finding: no outcome/pk node exists for blood-labyrinth barrier permeability
Mannitol increased the rate of entry and egress of gentamicin through BLB significantly (p = 0.0044) but the effects on the BBB did not reach statistical significance (p = 0.581).
PMID:29228990 · one of two readings recorded this
renal clearance of gentamicin from blood
no effect, p = 0.433, p = 0.433
Mannitol did not alter renal clearance of gentamicin from the blood (p = 0.433).
PMID:29228990 · both readings recorded this
urinary mannitol concentration after dietary sweetener use
increases, about 14 mg/mL after up to 20 g/day
It is also shown that the use of mannitol as a sweetener in amounts of up to 20 g per day results in a urinary concentration of about 14 mg/mL.
PMID:30548818 · one of two readings recorded this
urinary mannitol concentration in an athlete reference population, and following dietary mannitol sweetener intake, by anti-doping laboratory analysis
increases, about 14 mg/mL urinary concentration after up to 20 g/day dietary intake
Not recorded as a finding: this platform holds no node for the endpoint
It is also shown that the use of mannitol as a sweetener in amounts of up to 20 g per day results in a urinary concentration of about 14 mg/mL.
PMID:30548818 · one of two readings recorded this
urinary mannitol concentration in athlete doping-control reference population, by mass-spectrometry-based urinalysis
mean 72 ± 140 μg/mL, median 41 μg/mL (n = 6407), n = 6407
Not recorded as a finding: this platform holds no node for the endpoint
Urinary mannitol concentrations demonstrate larger variation with the mean value of 72 ± 140 μg/mL and median at 41 μg/mL (n = 6407).
PMID:30548818 · one of two readings recorded this
urinary mannitol concentration in athlete reference population
mean value of 72 ± 140 μg/mL and median at 41 μg/mL, n = 6407
Urinary mannitol concentrations demonstrate larger variation with the mean value of 72 ± 140 μg/mL and median at 41 μg/mL (n = 6407).
PMID:30548818 · one of two readings recorded this
urinary mannitol concentration in doping-control reference population
mean 72 ± 140 μg/mL, median 41 μg/mL (n = 6407), n = 6407
Urinary mannitol concentrations demonstrate larger variation with the mean value of 72 ± 140 μg/mL and median at 41 μg/mL (n = 6407).
PMID:30548818 · one of two readings recorded this
urinary mannitol concentration (population reference range)
mean 72 ± 140 μg/mL, median 41 μg/mL, n = 6407
Not recorded as a finding: descriptive population reference range, not a listed outcome node
Urinary mannitol concentrations demonstrate larger variation with the mean value of 72 ± 140 μg/mL and median at 41 μg/mL (n = 6407).
PMID:30548818 · one of two readings recorded this
urinary mannitol concentration reference range in athletes and its effect on urine specific gravity
increases, mannitol present in mg/mL quantities significantly increases urine specific gravity
Not recorded as a finding: this platform holds no node for the endpoint
An important observation is that mannitol present in mg/mL quantities significantly increases urine specific gravity, which makes a widely accepted normalization approach not applicable.
PMID:30548818 · one of two readings recorded this
Urinary mannitol concentration
increases, mean 72 ± 140 μg/mL, median 41 μg/mL, 99.7th percentile 1094 μg/mL; about 14 mg/mL after up to 20 g/day dietary intake, n = 6407
Urinary mannitol concentrations demonstrate larger variation with the mean value of 72 ± 140 μg/mL and median at 41 μg/mL (n = 6407).
PMID:30548818 · one of two readings recorded this
urine specific gravity in samples with elevated urinary mannitol
increases, significantly increases urine specific gravity
An important observation is that mannitol present in mg/mL quantities significantly increases urine specific gravity, which makes a widely accepted normalization approach not applicable.
PMID:30548818 · one of two readings recorded this
urine specific gravity
increases
Not recorded as a finding: not a listed outcome node
An important observation is that mannitol present in mg/mL quantities significantly increases urine specific gravity, which makes a widely accepted normalization approach not applicable.
PMID:30548818 · one of two readings recorded this
urine specific gravity
increases, mannitol present in mg/mL quantities significantly increases urine specific gravity
An important observation is that mannitol present in mg/mL quantities significantly increases urine specific gravity, which makes a widely accepted normalization approach not applicable.
PMID:30548818 · one of two readings recorded this
Detection of increased numbers of variants by macrophage:tumor cell ratio
increases
Detection of increased numbers of variants depended upon the macrophage:tumor cell ratio, with 50:1 or greater being necessary
PMID:3084067 · one of two readings recorded this
Frequency of thioguanine-resistant variants
increases
an increase in the frequency of thioguanine-resistant variants which arose following macrophage coculture to levels at least 5- to 10-fold above the spontaneous frequency
PMID:3084067 · one of two readings recorded this
Induction of drug-resistant variants with oxygen radical scavengers
decreases
The induction of drug-resistant variants could be inhibited by oxygen radical scavengers
PMID:3084067 · one of two readings recorded this
Loss of HGPRT activity in macrophage-induced thioguanine-resistant variants
decreases, n = 6
In six of the six macrophage-induced variants tested, resistance was associated with loss of hypoxanthine-guanine phosphoribosyl transferase activity
PMID:3084067 · one of two readings recorded this
post-operative acute kidney injury (AKI) or renal end points/surrogates
Given the available evidence, the peri-operative use of mannitol to prevent AKI cannot be considered an evidence based intervention in cardiac surgery, partial nephrectomy, and/or other major surgery.
PMID:31078413 · one of two readings recorded this
sensitivity and specificity of the mannitol bronchial challenge test for diagnosing asthma
sensitivity 8%-100%, specificity 75%-100% overall; sensitivity 19%-91%, specificity 75%-100% excluding case-control studies conducted in a clinical setting, n = 4589
Overall sensitivity and specificity ranged from 8% (95% confidence interval [CI] 1-27) to 100% (95% CI 93-100) and 75% (95% CI 67-82) to 100% (95% CI 85-100).
PMID:31476241 · one of two readings recorded this
sensitivity and specificity of the mannitol bronchial challenge test in diagnosing asthma
Overall sensitivity and specificity ranged from 8% to 100% and 75% to 100% across included studies, n = 4589
A total of 27 studies (4589 individuals, age 6-85 years, cross-sectional [n = 18] and case-controlled [n = 9] study design) were included.
PMID:31476241 · one of two readings recorded this
cerebral perfusion pressure (CPP) change
increases, pooled difference in means = 0.54 (95% CI: 0.15-0.92, P =.007), p = 0.007
The pooled difference in means = 0.54 (95% CI: 0.15–0.92, P =.007) indicated that 3% hypertonic saline is more effective than 20% mannitol in increasing CPP.
PMID:32871879 · one of two readings recorded this
duration of continuous ICP reduction
decreases, pooled difference in means = 0.84 (95% CI: 0.64-1.05, P <.00001)
The pooled difference in means = 0.84 (95% CI: 0.64–1.05, P <.00001) indicated that 3% hypertonic saline lasts longer time for ICP reduction than 20% mannitol.
PMID:32871879 · one of two readings recorded this
intracranial pressure (ICP) reduction after osmotic infusion
decreases, pooled difference in means = -0.19 (95% CI: -0.37 to -0.02, P =.03), p = 0.03
Not recorded as a finding: the comparison was against another active treatment
The pooled difference in means = −0.19 (95% CI: −0.37 to −0.02, P =.03) indicated that mannitol reduces ICP more than hypertonic saline.
PMID:32871879 · one of two readings recorded this
intracranial pressure (ICP) reduction
decreases, pooled difference in means = -0.19 (95% CI: -0.37 to -0.02, P =.03), p = 0.03
The pooled difference in means = −0.19 (95% CI: −0.37 to −0.02, P =.03) indicated that mannitol reduces ICP more than hypertonic saline.
PMID:32871879 · one of two readings recorded this
onset time of ICP reduction
no effect, pooled difference in means = 0.05 (95% CI: -0.14 to 0.23, P =.64), p = 0.64
The pooled difference in means = 0.05 (95% CI: −0.14 to 0.23, P =.64) indicated that There was no significant difference in onset time between 3% hypertonic saline and 20% mannitol.
PMID:32871879 · one of two readings recorded this
intracranial pressure (ICP), mean arterial blood pressure (MABP) and cerebral perfusion pressure (CPP), mean differences pooled from 8 studies, half-molar sodium lactate vs mannitol in severe traumatic brain injury
no effect
Not recorded as a finding: the comparison was against another active treatment
From the results of data analysis, the two treatment groups of mannitol and half-molar sodium lactate did not show any significant differences.
PMID:34344615 · one of two readings recorded this
intracranial pressure (ICP), mean arterial blood pressure (MABP), and cerebral perfusion pressure (CPP), pooled mean differences between mannitol and half-molar sodium lactate groups
no effect
Not recorded as a finding: the comparison was against another active treatment
From the results of data analysis, the two treatment groups of mannitol and half-molar sodium lactate did not show any significant differences.
PMID:34344615 · one of two readings recorded this
diagnostic sensitivity and specificity of the LMR test for coeliac disease
increases, pooled sensitivity 0.829 (95% CI 0.682-0.976), pooled specificity 0.700 (95% CI 0.551-0.849), pooled AUC 0.88 (95% CI 0.85-0.91)
Pooled specificity (Additional file 1: Fig S5A) was calculated as 0.700 (95% CI: 0.551–0.849), and pooled sensitivity (Additional file 1: Fig S5B) was calculated as 0.829 (95% CI: 0.682–0.976).
PMID:35012471 · one of two readings recorded this
lactulose:mannitol ratio (LMR) in healthy controls vs coeliac/Crohn's disease
increases, pooled LMR: healthy 0.014 (95% CI 0.006-0.022), untreated coeliac 0.133 (95% CI 0.089-0.178), active Crohn's 0.093 (95% CI 0.031-0.156)
Pooled analysis of gut permeability results in healthy subjects analysed in 24 studies revealed a LMR value of 0.014 (95% CI: 0.006 to 0.022).
PMID:35012471 · one of two readings recorded this
callose deposition in soybean seedlings under osmotic stress and flg22
increases, callose induced
The data show that callose is induced by both osmotic stress and flagellin 22 (flg22) and is related to the activity of β-1,3-glucanases.
PMID:36811487 · one of two readings recorded this
callose deposition in soybean seedlings
increases, callose is induced by both osmotic stress and flagellin 22 (flg22)
The data show that callose is induced by both osmotic stress and flagellin 22 (flg22) and is related to the activity of β-1,3-glucanases.
PMID:36811487 · one of two readings recorded this
GmGSL gene family expression (including GmGSL23) in soybean roots by RT-qPCR
increases, upregulated
The GmGSL23 gene was upregulated in seedlings treated with osmotic stress or flg22, showing the essential role of this gene in the soybean defense response to pathogenic organisms and osmotic stress.
PMID:36811487 · one of two readings recorded this
GmGSL23 gene expression and callose deposition in soybean seedling roots under osmotic stress (mannitol) treatment, by RT-qPCR
increases, GmGSL23 upregulated under osmotic stress or flg22
Not recorded as a finding: the supporting sentence never names the compound
The GmGSL23 gene was upregulated in seedlings treated with osmotic stress or flg22, showing the essential role of this gene in the soybean defense response to pathogenic organisms and osmotic stress.
PMID:36811487 · one of two readings recorded this
GmGSL23 gene expression (RT-qPCR) in soybean roots
increases, GmGSL23 gene was upregulated in seedlings treated with osmotic stress or flg22
The GmGSL23 gene was upregulated in seedlings treated with osmotic stress or flg22, showing the essential role of this gene in the soybean defense response to pathogenic organisms and osmotic stress.
PMID:36811487 · both readings recorded this
GmGSL23 (glucan synthase-like gene) expression, RT-qPCR
increases
The GmGSL23 gene was upregulated in seedlings treated with osmotic stress or flg22, showing the essential role of this gene in the soybean defense response to pathogenic organisms and osmotic stress.
PMID:36811487 · one of two readings recorded this
chromosomal aberration (CA) and micronucleus (MN) frequency, mitotic index (MI) and nuclear division index (NDI) in human peripheral lymphocytes exposed to mannitol in vitro
decreases, mannitol significantly decreased the MI compared to the control at almost all concentrations and treatment times
Not recorded as a finding: this platform holds no node for the endpoint
However, mannitol (except at concentrations of 500 and 1000 μg/mL) and lactitol (except at 250 μg/mL) significantly decreased the MI compared to the control at almost all concentrations and treatment times.
PMID:38060281 · one of two readings recorded this
Chromosomal aberration (CA) and micronucleus (MN) frequency; nuclear division index (NDI)
no effect
The results indicated that both polyols did not affect CA and MN frequency, and did not cause a significant change in NDI at all treatment concentratoins.
PMID:38060281 · one of two readings recorded this
chromosomal aberration (CA) frequency in human peripheral lymphocytes
no effect, did not affect CA frequency
The results indicated that both polyols did not affect CA and MN frequency, and did not cause a significant change in NDI at all treatment concentratoins.
PMID:38060281 · one of two readings recorded this
chromosomal aberration (CA) frequency
no effect, did not affect CA frequency
The results indicated that both polyols did not affect CA and MN frequency, and did not cause a significant change in NDI at all treatment concentratoins.
PMID:38060281 · one of two readings recorded this
chromosomal aberration (CA) frequency
no effect
The results indicated that both polyols did not affect CA and MN frequency, and did not cause a significant change in NDI at all treatment concentratoins.
PMID:38060281 · one of two readings recorded this
chromosomal aberration frequency, micronucleus frequency, mitotic index and nuclear division index in human peripheral lymphocytes exposed to mannitol in vitro
no effect, no significant genotoxic effect at tested concentrations
Not recorded as a finding: this platform holds no node for the endpoint
In conclusion, it was observed that mannitol and lactitol did not have a significant genotoxic effect at the concentrations used in human lymphocytes in vitro.
PMID:38060281 · one of two readings recorded this
micronucleus (MN) frequency in human peripheral lymphocytes
no effect, did not affect MN frequency
The results indicated that both polyols did not affect CA and MN frequency, and did not cause a significant change in NDI at all treatment concentratoins.
PMID:38060281 · one of two readings recorded this
micronucleus (MN) frequency
no effect, did not affect MN frequency
The results indicated that both polyols did not affect CA and MN frequency, and did not cause a significant change in NDI at all treatment concentratoins.
PMID:38060281 · one of two readings recorded this
micronucleus (MN) frequency
no effect
The results indicated that both polyols did not affect CA and MN frequency, and did not cause a significant change in NDI at all treatment concentratoins.
PMID:38060281 · one of two readings recorded this
mitotic index (MI), chromosomal aberration (CA) frequency, micronucleus (MN) frequency, and nuclear division index (NDI) in human peripheral lymphocytes exposed to mannitol in vitro
decreases
Not recorded as a finding: this platform holds no node for the endpoint
However, mannitol (except at concentrations of 500 and 1000 μg/mL) and lactitol (except at 250 μg/mL) significantly decreased the MI compared to the control at almost all concentrations and treatment times.
PMID:38060281 · one of two readings recorded this
mitotic index (MI) in human peripheral lymphocytes
decreases, significantly decreased MI at almost all concentrations, except 500 and 1000 μg/mL for mannitol
However, mannitol (except at concentrations of 500 and 1000 μg/mL) and lactitol (except at 250 μg/mL) significantly decreased the MI compared to the control at almost all concentrations and treatment times.
PMID:38060281 · one of two readings recorded this
Mitotic index (MI)
decreases
However, mannitol (except at concentrations of 500 and 1000 μg/mL) and lactitol (except at 250 μg/mL) significantly decreased the MI compared to the control at almost all concentrations and treatment times.
PMID:38060281 · one of two readings recorded this
mitotic index (MI)
decreases
However, mannitol (except at concentrations of 500 and 1000 μg/mL) and lactitol (except at 250 μg/mL) significantly decreased the MI compared to the control at almost all concentrations and treatment times.
PMID:38060281 · one of two readings recorded this
nuclear division index (NDI) in human peripheral lymphocytes
no effect, no significant change at all treatment concentrations
The results indicated that both polyols did not affect CA and MN frequency, and did not cause a significant change in NDI at all treatment concentratoins.
PMID:38060281 · one of two readings recorded this
nuclear division index (NDI)
no effect, did not cause a significant change in NDI at all treatment concentrations
The results indicated that both polyols did not affect CA and MN frequency, and did not cause a significant change in NDI at all treatment concentratoins.
PMID:38060281 · one of two readings recorded this
nuclear division index (NDI)
no effect
The results indicated that both polyols did not affect CA and MN frequency, and did not cause a significant change in NDI at all treatment concentratoins.
PMID:38060281 · one of two readings recorded this
duration of the ICP-reducing effect
decreases, MD = -0.67, 95% CI = [-1.00, -0.33], p < 0.01
The duration of the effect was shorter in the mannitol group than in the HS group (MD = -0.67, 95% CI = [-1.00, -0.33], p < 0.01).
PMID:38825027 · one of two readings recorded this
favorable neurological outcome (Glasgow Outcome Scale)
no effect, RR = 0.92, 95% CI = [0.11, 7.96], p = 0.94, p = 0.94
In terms of favorable neurological outcomes, there was no significant difference between the two agents (RR = 0.92, 95% CI = [0.11, 7.96], p = 0.94).
PMID:38825027 · one of two readings recorded this
ICU length of stay
increases, MD = 1.18, 95% CI = [0.44, 1.92], p < 0.01
The length of stay in the ICU was significantly shorter in the HS group (MD = 1.18, 95% CI = [0.44, 1.92], p < 0.01).
PMID:38825027 · one of two readings recorded this
mortality, ICU/hospital length of stay, Glasgow Outcome Scale, and duration of ICP-reduction effect in severe traumatic brain injury
no effect, RR = 1.55; 95% CI = [0.98, 2.47], p = 0.06
Not recorded as a finding: the comparison was against another active treatment
The mortality in the mannitol group was not statistically different compared to the HS group (RR = 1.55; 95% CI = [0.98, 2.47], p = 0.06).
PMID:38825027 · one of two readings recorded this
Other names
11 names
Resolves to: D-mannitol
- Also called
- (2R,3R,4R,5R)-hexane-1,2,3,4,5,6-hexaol(2R,3R,4R,5R)-hexane-1,2,3,4,5,6-hexolD-(-)-MannitoldulciteE 421E-421E421manna sugarmannitemannitol
- Sold as
- Osmitrol