|
|
| Tacrolimus | ||
| Order Code: TACRO
Order Form: A-1a Therapeutic Drug Analysis or IPR Req |
Chemistry 6240 RCP 356-3527 |
|
Specimen |
Whole Blood | ||
Collection Medium: |
| ||
Alternate Collection Media: |
Call laboratory for additional acceptable specimen collection containers. | ||
Minimum: |
Preferred minimum: 3 mL whole blood in lavendar top tube (EDTA), mix well. Absolute minimum: 1 mL whole blood | ||
Specimen Instructions: |
Collect before next dose. | ||
Testing Schedule: |
Availability: one batch per day. Cutoff time for same day service is 0900. Results available 1200 daily. | ||
Analytic Time: |
24 hours (upon receipt in laboratory) | ||
Reference Range: |
Therapeutic range 5-15 ng/ml | ||
Test Limitations: |
The immunoassays are nonspecific and cross react with metabolites. When elimination of tacrolimus is impaired (e.g. during cholestasis), tacrolimus metabolites may accumulate. The immunoassay may overestimate the concentration of tacrolimus. In such cases, the use of a specific assay (e.g. HPLC/MS/MS) could be considered. Specimens from patients who have received preparations of mouse monoclonal antibodies for diagnosis or therapy may contain human anti-mouse antibodies (HAMA). Such specimens may show either falsely elevated or depressed values when tested with assay kits which utilize mouse monoclonal antibodies. These specimens should not be assayed with the IMx Tacrolimus II assay. | ||
Methodology: |
MEIA (Microparticle Enzymatic ImmunoAssay) | ||
CPT Code: |
80197 |
Updated: 04/16/2008
Note: The information contained in this handbook is for use by personnel of University of Iowa Health Care. No other use is implied or intended.