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Serum Osmolality
Serum Osmolality
Used to assess the concentration of solutes in blood and helps evaluate fluid balance, electrolyte disturbances, and toxin ingestion

Serum Osmolality
Serum Osmolality
Used to assess the concentration of solutes in blood and helps evaluate fluid balance, electrolyte disturbances, and toxin ingestion
Instructions
To calculate, input serum sodium, glucose, and blood urea nitrogen (BUN) into the standard formula. Direct measurement can also be done via laboratory osmometry. Always compare the measured and calculated values to check for an osmolal gap, which can indicate the presence of unmeasured solutes such as toxic alcohols.
Overview
When to use
Why use
Evidences
Interpretation
Serum osmolarity = (2 × Na + (BUN / 2.8) + (glucose / 18))
Comparative analyses indicate the simple formula 2×Na + glucose/18 + BUN/2.8 performs as well as more complex equations for plasma osmolality estimation across general populations, supporting its use at the bedside
https://www.sciencedirect.com/science/article/abs/pii/S000991201500082X
Osmolal gap = measured osmolality (osmometer) − calculated osmolality. A normal gap is typically <10 mOsm/kg; larger gaps suggest unmeasured osmoles (e.g., toxic alcohols, mannitol, glycols, ketones), though lab and patient factors can affect the gap
https://pmc.ncbi.nlm.nih.gov/articles/PMC10166247/
Emergency/toxicology literature emphasizes that all alcohols, including ethanol, alter the osmolal gap; large gaps (>20) warrant evaluation for toxic alcohol ingestion along with anion gap and acid–base status
https://www.sciencedirect.com/science/article/abs/pii/S0196064424013039
During hyperosmolar therapy (mannitol or hypertonic saline), calculated osmolality may deviate from measured values; several studies show variable agreement depending on the formula used, advocating direct osmometry or validated formulas and attention to the osmolal gap when monitoring therapy
Overview
When to use
Why use
Evidences
Serum osmolality reflects the number of dissolved particles in plasma and is a key indicator of the body’s hydration and electrolyte status. It plays a critical role in maintaining osmotic equilibrium between intracellular and extracellular compartments, guided primarily by sodium, glucose, and urea levels.
The osmolal gap is the difference between measured and calculated osmolality. A gap >10–15 mOsm/kg typically indicates unmeasured solutes, most importantly toxic alcohols.
Clinically, serum osmolality is used in the evaluation of hyponatremia, hypernatremia, suspected poisoning, and altered mental status. It helps guide fluid therapy and the management of electrolyte imbalances. Its utility spans emergency medicine, nephrology, toxicology, and endocrinology.
Overview
When to use
Why use
Evidences
Interpretation
Serum osmolarity = (2 × Na + (BUN / 2.8) + (glucose / 18))
Comparative analyses indicate the simple formula 2×Na + glucose/18 + BUN/2.8 performs as well as more complex equations for plasma osmolality estimation across general populations, supporting its use at the bedside
https://www.sciencedirect.com/science/article/abs/pii/S000991201500082X
Osmolal gap = measured osmolality (osmometer) − calculated osmolality. A normal gap is typically <10 mOsm/kg; larger gaps suggest unmeasured osmoles (e.g., toxic alcohols, mannitol, glycols, ketones), though lab and patient factors can affect the gap
https://pmc.ncbi.nlm.nih.gov/articles/PMC10166247/
Emergency/toxicology literature emphasizes that all alcohols, including ethanol, alter the osmolal gap; large gaps (>20) warrant evaluation for toxic alcohol ingestion along with anion gap and acid–base status
https://www.sciencedirect.com/science/article/abs/pii/S0196064424013039
During hyperosmolar therapy (mannitol or hypertonic saline), calculated osmolality may deviate from measured values; several studies show variable agreement depending on the formula used, advocating direct osmometry or validated formulas and attention to the osmolal gap when monitoring therapy
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