Test Id : HIPA
Hippuric Acid, Urine
Method Name
A short description of the method used to perform the test
Colorimetry (C)
High Performance Liquid Chromatography/Tandem Mass Spectrometry (LC-MS/MS)
NY State Available
Indicates the status of NY State approval and if the test is orderable for NY State clients.
Reporting Name
Lists a shorter or abbreviated version of the Published Name for a test
Aliases
Lists additional common names for a test, as an aid in searching
Benzyl Alcohol Metabolite
Hippurate
Hippuric Acid, Urine
n-Benzoylglycine
Toluene Metabolite
Specimen Type
Describes the specimen type validated for testing
Urine
Specimen Required
Defines the optimal specimen required to perform the test and the preferred volume to complete testing
***Must submit one specimen per order. Specimens cannot be shared between multiple orders.***
Specimen Type: Urine
Container/Tube: Plastic preservative-free urine container
Specimen Volume: 3 mL
Collection Instructions: Collect 3 mL random urine specimen at end of shift. Send specimen refrigerated in a plastic, preservative-free urine container.
Specimen Minimum Volume
Defines the amount of sample necessary to provide a clinically relevant result as determined by the testing laboratory. The minimum volume is sufficient for one attempt at testing.
1.1 mL
Reject Due To
Identifies specimen types and conditions that may cause the specimen to be rejected
Specimen Stability Information
Provides a description of the temperatures required to transport a specimen to the performing laboratory, alternate acceptable temperatures are also included
| Specimen Type | Temperature | Time | Special Container |
|---|---|---|---|
| Urine | Refrigerated (preferred) | 30 days | |
| Ambient | 5 days | ||
| Frozen | 30 days |
Reference Values
Describes reference intervals and additional information for interpretation of test results. May include intervals based on age and sex when appropriate. Intervals are Mayo-derived, unless otherwise designated. If an interpretive report is provided, the reference value field will state this.
Reporting limit determined each analysis
Creatinine (mg/L):
U.S. Population (10th – 90th percentiles, median)
All participants:
335 - 2370 mg/L, median: 1180 (n=22,245)
Males:
Females:
273 - 2170 mg/L, median 994 (n=11,635)
Hippuric Acid (g/L)
Normal for unexposed populations is generally less than 1.6 g/L.
Hippuric Acid (Creatinine corrected) (g/g Creat)
Normal for unexposed populations is generally less than 1.5 g/g creatinine.
Specific Gravity Confirmation
Physiologic range: 1.010 - 1.030
PDF Report
Indicates whether the report includes an additional document with charts, images or other enriched information
Day(s) Performed
Outlines the days the test is performed. This field reflects the day that the sample must be in the testing laboratory to begin the testing process and includes any specimen preparation and processing time before the test is performed. Some tests are listed as continuously performed, which means that assays are performed multiple times during the day.
Monday through Sunday
Report Available
The interval of time (receipt of sample at Mayo Clinic Laboratories to results available) taking into account standard setup days and weekends. The first day is the time that it typically takes for a result to be available. The last day is the time it might take, accounting for any necessary repeated testing.
Specimen Retention Time
Outlines the length of time after testing that a specimen is kept in the laboratory before it is discarded
Performing Laboratory Location
Indicates the location of the laboratory that performs the test
Fees :
Several factors determine the fee charged to perform a test. Contact your U.S. or International Regional Manager for information about establishing a fee schedule or to learn more about resources to optimize test selection.
- Authorized users can sign in to Test Prices for detailed fee information.
- Clients without access to Test Prices can contact Customer Service 24 hours a day, seven days a week.
- Prospective clients should contact their account representative. For assistance, contact Customer Service.
Test Classification
Provides information regarding the medical device classification for laboratory test kits and reagents. Tests may be classified as cleared or approved by the US Food and Drug Administration (FDA) and used per manufacturer instructions, or as products that do not undergo full FDA review and approval, and are then labeled as an Analyte Specific Reagent (ASR) product.
This test was developed and its performance characteristics determined by NMS Labs. It has not been cleared or approved by the U.S. Food and Drug Administration.
CPT Code Information
Provides guidance in determining the appropriate Current Procedural Terminology (CPT) code(s) information for each test or profile. The listed CPT codes reflect Mayo Clinic Laboratories interpretation of CPT coding requirements. It is the responsibility of each laboratory to determine correct CPT codes to use for billing.
CPT codes are provided by the performing laboratory.
CPT codes are provided by the performing laboratory.
82570
83921
81002 (if appropriate)
LOINC® Information
Provides guidance in determining the Logical Observation Identifiers Names and Codes (LOINC) values for the order and results codes of this test. LOINC values are provided by the performing laboratory.
| Test Id | Test Order Name | Order LOINC Value |
|---|---|---|
| HIPA | Hippuric Acid, U | Not Provided |
| Result Id | Test Result Name |
Result LOINC Value
Applies only to results expressed in units of measure originally reported by the performing laboratory. These values do not apply to results that are converted to other units of measure.
|
|---|---|---|
| Z1305 | Creatinine | 2161-8 |
| Z1341 | Reporting Limit | 19147-8 |
| Z1309 | Hippuric Acid | 6709-0 |
| Z1342 | Reporting Limit | 19147-8 |
| Z1306 | Hippuric Acid(Creatinine corrected) | 13754-7 |
| Z1343 | Reporting Limit | 19147-8 |
| Z2513 | Specific Gravity Confirmation | In Process |