Ordering Recommendation

Investigate primary and secondary aldosteronism. Distinguish between bilateral idiopathic hyperaldosteronism (IHA) and aldosterone-producing adenomas (APA).

New York DOH Approval Status

This test is New York state approved.

Specimen Required

Patient Preparation

Adrenal venous sampling procedure is required.

Collect

Serum Separator Tube (SST) or Plain Red.

Specimen Preparation

Separate from cells ASAP or within 2 hours of collection. Transfer 1 mL serum to an ARUP Standard Transport Tube. (Min: 0.5 mL)

Storage/Transport Temperature

Frozen.

Unacceptable Conditions

EDTA plasma.

Remarks
Stability

After separation from cells: Ambient: 8 hours; Refrigerated: 5 days; Frozen: 1 month

Methodology

Quantitative Chemiluminescent Immunoassay

Performed

Sun-Sat

Reported

Within 24 hours

Reference Interval

Interpretive Data



Compliance Category

FDA

Note

Refer to the Additional Technical Information for Endocrine Society recommendations for patient preparation, specimen collection, medications for hypertension control during confirmatory testing for primary aldosteronism, and factors that may lead to false-positive or false-negative aldosterone-renin ratio (ARR) results.

Hotline History

N/A

CPT Codes

82088

Components

Component Test Code* Component Chart Name LOINC
3000489 Aldosterone_Right Adrenal Vein 92897-8
* Component test codes cannot be used to order tests. The information provided here is not sufficient for interface builds; for a complete test mix, please click the sidebar link to access the Interface Map.

Aliases

Aldosterone Right Adrenal Vein