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Test Directory

Sodium, Feces

Order Code: NAFEC

Test Summary

This test measures sodium in liquid stool. Measurements of electrolytes and osmotic gap in liquid stool help differentiate between secretory and osmotic diarrhea and, thus, guide further evaluation of chronic diarrhea [1,2].

Diarrhea can be categorized as secretory or osmotic depending on how the water content of stool is drawn in the intestine lumen. Secretory diarrhea is caused by defective electrolyte absorption that increases the stool's electrolyte levels. Conditions associated with secretory diarrhea include infection, neuroendocrine tumors, congenital chloridorrhea, intestinal resection, and diffuse mucosal disease [1]. Osmotic diarrhea is caused by the osmotic effect of a substance that retains water in the intestine lumen and leads to decreased electrolyte levels in the stool. Conditions associated with osmotic diarrhea include ingesting poorly absorbed solutes (eg, sorbitol, mannitol, and laxatives containing magnesium) and enzyme dysfunction (eg, lactose intolerance) [2].

Stool sodium level is often measured in conjunction with stool potassium level to calculate osmotic gap, which is the difference between the stool osmolality and twice the sum of the stool sodium and potassium levels. Osmotic gap is useful in assessing the contribution of stool electrolytes to osmolality and differentiating between secretory and osmotic diarrhea [1,2].

The results of this test should be interpreted in the context of pertinent clinical and family history and physical examination findings.

References
1. Schiller LR. Pract Res Clin Gastroenterol. 2012;26(5):551-562.
2. Block DR, et al. Body fluids. In: Rifai R, et al. eds. Tietz Textbook of Laboratory Medicine. 7th ed. Elsevier Inc; 2022.

Aliases

  • N/A

Specimen Collection

Order Code

NAFEC

EPIC (Premier) Code

LAB3686

Includes

N/A

CPT Code

  • 84302

Billing Code

  • 670348

CPT Statement

Methodology

Flame Photometric

FDA Status

This test was developed and its analytical performance characteristics have been determined by Quest Diagnostics. It has not been cleared or approved by FDA. This assay has been validated pursuant to the CLIA regulations and is used for clinical purposes.

Physician Attestation of Informed Consent

N/A

Testing Laboratory

Quest Diagnostics Nichols Institute
14225 Newbrook Drive
Chantilly VA, 20153

Department

Reference Testing

Reference Range

See Laboratory Report

Setup Schedule / Expected Turnaround Time

Monday - Friday, Sunday evening Report available: 3 days

Specimen Collection

Billing

CPT Code

  • 84302

Billing Code

  • 670348

CPT Statement

Result Information

Methodology

Flame Photometric

Testing Laboratory

N/A

Reference Range

See Laboratory Report

Setup Schedule / Expected Turnaround Time

Monday - Friday, Sunday evening Report available: 3 days