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|
| Phenytoin, Free | ||
| Order Code: FDPH
Order Form: A-1a Therapeutic Drug Analysis or IPR Req |
Chemistry 6240 RCP 356-3527 |
|
Specimen |
Plasma | ||
Collection Medium: |
| ||
Alternate Collection Media: |
Call laboratory for additional acceptable specimen collection containers. | ||
Minimum: |
2 ml whole blood from light green top tube | ||
Testing Schedule: |
Monday-Friday, 0800-1200. | ||
Analytic Time: |
24 hours (upon receipt in laboratory) | ||
Reference Range: |
1.0-1.9 mcg/ml Average percent free is 9.6% with a range of 7.0-14.6% (N=91). Critical value: >1.9 mcg/ml | ||
Comments: |
Note: Phenytoin plasma specimens should not be drawn for 2 hours following completion of an I.V. fosphenytoin infusion or 4 hours following an I.M. fosphenytoin dose (See Fosphenytoin). To accurately determine the percentage of free phenytoin, a total phenytoin should be ordered on the same sample. | ||
Test Limitations: |
Criterion: recovery plus or minus 0.6 ug/ml of initial value at concentrations less than 6 ug/ml or plus or minus 10% of initial value at concentrations greater than 6 ug/ml. Icterus: No significant interference from bilirubin up to an I index of 30 (approximate bilirubin concentration: 60 mg/dl). Hemolysis: No significant interference from hemoglobin up to an H index of 800 (approximate hemoglobin concentration: 1000 mg/dl). Lipemia (Intralipid): No significant interference from lipemia up to an L index of 750. (approximate triglycerides concentration: 2000 mg/dl). There is poor correlation between turbidity and triglycerides concentration. | ||
Methodology: |
EIA (Enzymatic ImmunoAssay) | ||
CPT Code: |
80186 | ||
See also: Phenytoin, Plasma | |||
See Additional Information: Chemistry Critical Lab Values |
Updated: 02/28/2007
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.