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Citric Acid, Urine with Creatinine

Test Summary

This quantitative citric acid test, performed with a random urine specimen, may help assess the risk of calcium stone formation in the kidneys and inform patient management [1]. In general, 24-hour urine specimens (Citric Acid, 24-Hour Urine with Creatinine) are preferred to random urine specimens when measuring citric acid for diagnostic evaluation and monitoring of calcium nephrolithiasis [2].

Citrate inhibits calcium stone formation by binding and solubilizing calcium, which reduces supersaturation of calcium salts [1-2]. Approximately half of the patients with calcium stones have decreased urinary citrate levels [1]. Citrate is among several substances routinely screened to evaluate the risk of forming kidney stones. Low urinary citrate levels may indicate oral citrate treatment in patients with recurrent calcium nephrolithiasis [1]. Other conditions that can cause hypocitraturia include distal renal tubular acidosis, malabsorption, and urinary tract infection [1].

The urinary citric acid level cannot be used to estimate dietary intake because other factors, such as acid-base balance, may affect citrate excretion [2].

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

References
1. Delaney, PM et al. Kidney disease. In: Rifai R, et al. eds. Tietz Textbook of Laboratory Medicine. 7th ed. Elsevier Inc; 2022.
2. Williams JC Jr, et al. Urolithiasis. 2021;49(1):1-16.

Aliases

  • N/A

Specimen Collection

Special Instructions

N/A

Preferred Specimen

10 mL clean catch urine collected in a sterile screw-cap container

Minimum Volume

1.5 mL

Instructions

N/A

Patient Preparation

N/A

Storage

N/A

Transport Temperature

Refrigerated (cold packs)

Specimen Stability

  • Room temperature: 8 hours
  • Refrigerated: 30 days
  • Frozen: 60 days

Limitations

N/A

Other Acceptable Specimens

N/A

Unacceptable Specimens

Received room temperature • Acidified urine

Order Code

CITACD

EPIC (Premier) Code

LAB108

Includes

N/A

CPT Code

  • 82507
  • 82570 - This test is not available for New York patient testing.

Billing Code

  • 670202
  • 670203

CPT Statement

Methodology

Spectrophotometry (SP)

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 the U.S. Food and Drug Administration. The FDA has determined that such clearance or approval is not necessary. 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 - Saturday; Report available: 2 - 4 days

Specimen Collection

Special Instructions

N/A

Preferred Specimen

10 mL clean catch urine collected in a sterile screw-cap container

Minimum Volume

1.5 mL

Instructions

N/A

Patient Preparation

N/A

Storage

N/A

Transport Temperature

Refrigerated (cold packs)

Specimen Stability

  • Room temperature: 8 hours
  • Refrigerated: 30 days
  • Frozen: 60 days

Limitations

N/A

Other Acceptable Specimens

N/A

Unacceptable Specimens

Received room temperature • Acidified urine

Billing

CPT Code

  • 82507
  • 82570 - This test is not available for New York patient testing.

Billing Code

  • 670202
  • 670203

CPT Statement

Result Information

Methodology

Spectrophotometry (SP)

Testing Laboratory

N/A

Reference Range

See Laboratory Report

Setup Schedule / Expected Turnaround Time

Monday - Saturday; Report available: 2 - 4 days