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Test Code OSMOF Osmolality, Feces

Additional Codes

Cerner NextGen
Osmolality Feces Osmolality Feces

 


Ordering Guidance


This test is only clinically valid if performed on watery specimens. In the event a formed fecal specimen is submitted, the test will not be performed.



Specimen Required


Patient Preparation: No barium, laxatives, or enemas may be used for 96 hours prior to start of, or during, collection.

Supplies: Stool containers - 24, 48, 72 Hour Kit (T291)

Container/Tube: Stool container

Specimen Volume: 10 g

Collection Instructions: Collect a very liquid stool specimen.


Secondary ID

606758

Useful For

Measurement of osmolality for the workup of cases of chronic diarrhea

 

Diagnosis of factitious diarrhea (where patient adds fluid to stool to simulate diarrhea)

Method Name

Freezing Point Depression

Reporting Name

Osmolality, F

Specimen Type

Fecal

Specimen Minimum Volume

5 g

Specimen Stability Information

Specimen Type Temperature Time Special Container
Fecal Frozen (preferred) 14 days
  Refrigerated  7 days
  Ambient  48 hours

Reject Due To

All specimens will be evaluated at Mayo Clinic Laboratories for test suitability.

Clinical Information

The concentration of electrolytes in fecal water and their rate of excretion are dependent upon 3 factors:

-Normal daily dietary intake of electrolytes

-Passive transport from serum and other vascular spaces to equilibrate fecal osmotic pressure with vascular osmotic pressure

-Electrolyte transport into fecal water due to exogenous substances and rare toxins (eg, cholera toxin)

 

Fecal osmolality is normally in equilibrium with vascular osmolality, and sodium is the major effector of this equilibrium. Fecal osmolality is normally 2 x (sodium + potassium) unless there are exogenous factors inducing a change in composition, such as the presence of other osmotic agents (magnesium sulfate, saccharides) or drugs inducing secretions, such as phenolphthalein or bisacodyl.

 

Differentiating osmotic from non-osmotic causes of diarrhea is the goal of liquid stool testing.(1,2) The primary way this is accomplished is through the measurement of sodium and chloride and calculation of the osmotic gap, which uses an assumed normal osmolality of 290 mOsm/kg rather than direct measurement of the osmolality.

Measurement of osmolality can be useful in the evaluation of chronic diarrhea to help identify whether a specimen has been diluted with hypotonic fluid to simulate diarrhea.(1,3)

Reference Values

An interpretive report will be provided

Interpretation

Stool osmolality below 220 mOsm/kg indicates dilution with a hypotonic fluid.(1)

Specimen Retention Time

7 days

Performing Laboratory

Mayo Clinic Laboratories in Rochester

Test Classification

This test has been modified from the manufacturer's instructions. Its performance characteristics were determined by Mayo Clinic in a manner consistent with CLIA requirements. This test has not been cleared or approved by the US Food and Drug Administration.

CPT Code Information

84999

LOINC Code Information

Test ID Test Order Name Order LOINC Value
OSMOF Osmolality, F 2693-0

 

Result ID Test Result Name Result LOINC Value
OSMOF Osmolality, F 2693-0

Day(s) Performed

Monday, Thursday

Report Available

1 to 3 days
Fairbanks Memorial Hospital Additional Information: