Search our extensive Laboratory Test Directory to find test codes, ordering recommendations, specimen stability information, Test Fact Sheets, and more.
Recommendations when to order or not order the test. May include related or preferred tests.
First-line test in suspected pheochromocytoma.
New York DOH Approval Status
Indicates whether a test has been approved by the New York State Department of Health.
This test is New York state approved.
Specimen Required
Patient PreparationInstructions patient must follow before/during specimen collection.
If possible, abstain from medications for 72 hours prior to collection.
CollectSpecimen type to collect. May include collection media, tubes, kits, etc.
24-hour or random urine. Refrigerate 24-hour specimen during collection.
Specimen PreparationInstructions for specimen prep before/after collection and prior to transport.
Thoroughly mix entire collection (24-hour or random) in one container. Transfer a 4 mL aliquot to an ARUP standard transport tube. (Min: 2.5 mL) A pH lower than 2 can cause assay interference. Record total volume and collection time interval on transport tube and test request form. Specimen preservation can be extended to 1 month refrigerated by performing one of the following: Option 1: Transfer a 4 mL aliquot to an ARUP standard transport tube. (Min: 2.5 mL) Adjust pH to 2.0-4.0 with 6M HCl. Option 2: Transfer a 4 mL aliquot to an ARUP standard transport tube containing 20 mg sulfamic acid (ARUP Supply #48098), available online through eSupply using ARUP Connect™ or contact ARUP Client Services at 800-522-2787. (Min: 2.5 mL)
Storage/Transport TemperaturePreferred temperatures for storage prior to and during shipping to ARUP. See Stability for additional info.
Refrigerated. Also acceptable: Frozen.
Unacceptable ConditionsCommon conditions under which a specimen will be rejected.
Specimens preserved with boric acid or acetic acid.
RemarksAdditional specimen collection, transport, or test submission information.
StabilityAcceptable times/temperatures for specimens. Times include storage and transport time to ARUP.
Quantitative High Performance Liquid Chromatography-Tandem Mass Spectrometry
Performed
Days of the week the test is performed.
Sun-Sat
Reported
Expected turnaround time for a result, beginning when ARUP has received the specimen.
1-5 days
Reference Interval
Normal range/expected value(s) for a specific disease state. May also include abnormal ranges.
Test Number
Components
Reference Interval
Creatinine, Urine - per 24h
Age
Male (mg/d)
Female (mg/d)
3-8 years
140-700
140-700
9-12 years
300-1300
300-1300
13-17 years
500-2300
400-1600
18-50 years
1000-2500
700-1600
51-80 years
800-2100
500-1400
81 years and older
600-2000
400-1300
Metanephrine, Urine - per 24h
Age
Male (µg/d)
Female (µg/d)
0-6 years
Not Applicable
Not Applicable
7-12 years
45-273
40-209
13-17 years
56-298
40-209
18 years and older
55-320
36-229
Metanephrine, Urine - ratio to CRT
Age
µg/g CRT
0-3 months
0-700
4-6 months
0-650
7-11 months
0-650
1 year
0-530
2-5 years
0-500
6-17 years
0-320
18 years and older
0-300
Normetanephrine, Urine - per 24h
Age
Male (µg/d)
Female (µg/d)
0-6 years
Not Applicable
Not Applicable
7-12 years
58-670
48-474
13-17 years
82-553
65-406
18-29 years
81-667
18 years and older: 95-650
30 years and older
114-865
Not Applicable
Normetanephrine, Urine - ratio to CRT
Age
µg/g CRT
0-3 months
0-3400
4-6 months
0-2200
7-11 months
0-1100
1 year
0-1300
2-5 years
0-610
6-17 years
0-450
18 years and older
0-400
Interpretive Data
May include disease information, patient result explanation, recommendations, or details of testing.
Smaller increases in metanephrine and/or normetanephrine concentrations (less than two times the upper reference limit) usually are the result of physiological stimuli, drugs, or improper specimen collection. Essential hypertension is often associated with slight elevations (metanephrine less than 400 ug/d and normetanephrine less than 900 ug/d). Elevated concentrations may be due to intense physical activity, life-threatening illness, and drug interferences.
Significant elevation of one or both metanephrines (three or more times the upper reference limit) is associated with an increased probability of a neuroendocrine tumor.
Per 24h calculations are provided to aid interpretation for collections with a duration of 24 hours and an average daily urine volume. For specimens with notable deviations in collection time or volume, ratios of analytes to a corresponding urine creatinine concentration may assist in result interpretation.
Compliance Category
Laboratory Developed Test (LDT)
Note
Additional information related to the test.
Hotline History
N/A
CPT Codes
The American Medical Association Current Procedural Terminology (CPT) codes published in ARUP's Laboratory Test Directory are provided for informational purposes only. The codes reflect our interpretation of CPT coding requirements based upon AMA guidelines published annually. CPT codes are provided only as guidance to assist clients with billing. ARUP strongly recommends that clients confirm CPT codes with their Medicare administrative contractor, as requirements may differ. CPT coding is the sole responsibility of the billing party. ARUP Laboratories assumes no responsibility for billing errors due to reliance on the CPT codes published.
* 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.