Test Directory
| Test Code | |||
| VEDLZ | |||
| Test Name | |||
| Vedolizumab | |||
| CPT Codes | |||
| 80280, 82397 | |||
| Included Tests | |||
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| Expected Turnaround Time | |||
| 5 - 8 days | |||
| Clinical Utility | |||
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Useful for assessing for primary or secondary loss of response to therapy with vedolizumab and as an aid to achieving desired serum concentrations of vedolizumab. |
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| Specimen and Container Info | |||
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Specimen Type: Serum
Preferred Collection Container: Red Top, Plain Alternate Collection Container: Gold Top, Serum Separator Desired Specimen Volume: 1.5 mL |
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| Collection Instructions | |||
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| Processing and Submission Instructions | |||
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| Patient Preparation | |||
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| Transport Instructions | |||
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Transport to the laboratory refrigerated. |
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| Stability Requirements | |||
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| Methodology | |||
| Varies By Test | |||
| Reference Intervals | |||
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See patient report. |
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| Limitations | |||
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Patients actively undergoing therapy with both vedolizumab and nivolumab (rare scenario) should not have their therapeutic vedolizumab concentration assessed using this test. If the patient has taken nivolumab in the past, they should wait for 4 weeks after therapy with nivolumab has ended before being tested for vedolizumab quantitation using this method. Samples containing more than 100 ng/mL biotin (vitamin B7) may interfere with ATV (in the form of depressed signal) for VEMAB / Vedolizumab Antibodies, Serum. |
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| Alternate Names | |||
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| Reference Lab | |||
| Mayo Clinic Laboratories | |||
| Testing Schedule | |||
| Varies | |||
The American Medical Association (AMA) Current Procedural Terminology (CPT) codes published by HNL Lab Medicine are guidelines and are intended for informational purposes only. CPT coding is the exclusive responsibility of the billing entity. View the Terms.
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