Refer to Specimen Stability criteria as shown below
Ambient
72 hours
Refrigerated
7 days
Frozen
14 days
Unacceptable Conditions
Specimens that exceed stated stability, unlabeled/mislabeled/mismatched specimens, specimens submitted in leaking containers
Special Instructions
Collecting sample just before the next dose will be adequate for monitoring purposes. Optimal response to Everolimus is usually associated with the trough blood concentration (i.e., the minimum concentration experienced just before the next dose).
CPT Codes
80169
Synonyms
Zortress
Afinitor
Certican
Methodology
Liquid Chromatography/Tandem Mass Spectrometry (LCMS/MS)
Performing Location
Chemistry (Toxicology)
Reported STAT
2 hours
Reported Routine
6 hours
Additional Information
This test was performed using liquid chromatography tandem mass spectrometry. This test was developed and its performance characteristics were determined by the University of California Irvine Medical Center, Department of Pathology and Laboratory Medicine. It has not been approved by the FDA, however, approval is not required for clinical use.
Test set up frequency
Daily (Cut-off time 12:00 Noon)
Reference Interval
Reference Range: 3.0-8.0 ng/mL
Therapeutic Ranges:
Kidney Transplant (in combination with Cyclosporine): 3-8 ng/mL
Liver Transplant ( in combination with Cyclosporine): 3-8 ng/mL
Critical Value (automatic call-back):
Toxic Value: Greater than 15 ng/mL
Additional Information
This test was performed using liquid chromatography tandem mass spectrometry. This test was developed and its performance characteristics were determined by the University of California Irvine Medical Center, Department of Pathology and Laboratory Medicine. It has not been approved by the FDA, however, approval is not required for clinical use.
Collection
Collect
3.0 mL whole blood in lavender-top (EDTA) tube(s)
Specimen Required
1.0 mL whole blood
Specimen Min Vol
0.5 mL Whole Blood
Specimen Preparation
None
Storage/Transport Temperature
Refer to Specimen Stability criteria as shown below
Ambient
72 hours
Refrigerated
7 days
Frozen
14 days
Unacceptable Conditions
Specimens that exceed stated stability, unlabeled/mislabeled/mismatched specimens, specimens submitted in leaking containers
Special Instructions
Collecting sample just before the next dose will be adequate for monitoring purposes. Optimal response to Everolimus is usually associated with the trough blood concentration (i.e., the minimum concentration experienced just before the next dose).
Test Info
CPT Codes
80169
Synonyms
Zortress
Afinitor
Certican
Methodology
Liquid Chromatography/Tandem Mass Spectrometry (LCMS/MS)
Performing Location
Chemistry (Toxicology)
Reported STAT
2 hours
Reported Routine
6 hours
Additional Information
This test was performed using liquid chromatography tandem mass spectrometry. This test was developed and its performance characteristics were determined by the University of California Irvine Medical Center, Department of Pathology and Laboratory Medicine. It has not been approved by the FDA, however, approval is not required for clinical use.
Test set up frequency
Daily (Cut-off time 12:00 Noon)
Result Interpretation
Reference Interval
Reference Range: 3.0-8.0 ng/mL
Therapeutic Ranges:
Kidney Transplant (in combination with Cyclosporine): 3-8 ng/mL
Liver Transplant ( in combination with Cyclosporine): 3-8 ng/mL
Critical Value (automatic call-back):
Toxic Value: Greater than 15 ng/mL
Additional Information
This test was performed using liquid chromatography tandem mass spectrometry. This test was developed and its performance characteristics were determined by the University of California Irvine Medical Center, Department of Pathology and Laboratory Medicine. It has not been approved by the FDA, however, approval is not required for clinical use.
