Osmometry: Difference between revisions
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Osmometry measures the osmotic strength of the particles within a sample. In clinical labs, this is most commonly performed using freezing point depression methodology. | Osmometry measures the osmotic strength of the particles within a sample. In clinical labs, this is most commonly performed using freezing point depression methodology. | ||
Uses | === Methodologies === | ||
Various techniques can be used to measure osmolality. | |||
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!Technique | |||
!Mechanism | |||
!Strengths | |||
!Limitations | |||
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|Freezing Point | |||
|Measures solute by freezing the sample and determining the freezing point. | |||
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* Accurate | |||
* Can be used to measure volatile solutes | |||
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|Vapour Pressure | |||
|Measures the decrease in vapour pressure when more solute is present. | |||
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|Unreliable when measuring volatile compounds (e.g., alcohols, acetone, etc.) | |||
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=== Uses === | |||
There are a variety of uses for osmometry and made include serum osmolality, urine osmolality, or both. | |||
* Investigating suspected toxin ingestion: | |||
**Alcohols (ethanol, methanol, isopropanol) | |||
**Ethylene and propylene glycol (antifreeze) | |||
**ASA and other salicylic acids | |||
**Paraldehyde | |||
* Investigation of renal function | |||
* Investigation of diabetes mellitus or diabetes insipidus | |||
*Monitoring osmotically active compounds: | |||
**Mannitol (as treatment for cerebral edema or when used for surgical irrigation) | |||
*Assessment of hyponatremia | |||
**Can differentiate true hyponatremia from pseudohyponatremia | |||
{| class="wikitable" | {| class="wikitable" | ||
! rowspan="2" |Serum Osmolality | ! rowspan="2" |Serum Osmolality | ||
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|Toxin ingestion: | |Toxin ingestion: | ||
* | *Alcohols (ethanol, methanol, isopropanol) | ||
* | *Ethylene and propylene glycol (antifreeze) | ||
*ASA and other salicylic acids | |||
*Paraldehyde | |||
Monitoring osmotically active compounds: | |||
* Mannitol (as treatment for cerebral edema) | |||
** Therapeutic: osmolar gap ~10 mOsm/kg | |||
** Renal toxicity: osmolar gap ≥50 mOsm/kg | |||
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Latest revision as of 23:44, 2 February 2026
Osmometry measures the osmotic strength of the particles within a sample. In clinical labs, this is most commonly performed using freezing point depression methodology.
Methodologies
Various techniques can be used to measure osmolality.
| Technique | Mechanism | Strengths | Limitations |
|---|---|---|---|
| Freezing Point | Measures solute by freezing the sample and determining the freezing point. |
|
|
| Vapour Pressure | Measures the decrease in vapour pressure when more solute is present. | Unreliable when measuring volatile compounds (e.g., alcohols, acetone, etc.) | |
Uses
There are a variety of uses for osmometry and made include serum osmolality, urine osmolality, or both.
- Investigating suspected toxin ingestion:
- Alcohols (ethanol, methanol, isopropanol)
- Ethylene and propylene glycol (antifreeze)
- ASA and other salicylic acids
- Paraldehyde
- Investigation of renal function
- Investigation of diabetes mellitus or diabetes insipidus
- Monitoring osmotically active compounds:
- Mannitol (as treatment for cerebral edema or when used for surgical irrigation)
- Assessment of hyponatremia
- Can differentiate true hyponatremia from pseudohyponatremia
| Serum Osmolality | RI: 275 - 295 mOsm/kg | |
|---|---|---|
| ▲ Increased | ▼ Decreased | |
| Conditions | Toxin ingestion:
Monitoring osmotically active compounds:
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| Lab Interferences | ||
| Other Factors |
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