Infliximab
Ordering Info & Methodology
Test Code
Cerner Synonyms
IFXB
Remicade Level, Infliximab (Reflexes to antibodies-to-infliximab), Remicade, Inflectra, Renflexis, infliximab-dyyb, infliximab-abda, anti-infliximab antibodies, anti-drug antibodies, ATI, IFX
Turn Around Time
Methodology
Analysis performed weekly. Not available as a STAT order.
Infliximab measured by a laboratory-developed mass spectrometry method; Total antibodies-to-infliximab measured by a semi-quantitative ELISA (Immunodiagnostik)
Ordering Guide
IFXB
Specimen Requirements
Sample Type
Collection Container
Alternate Collection Containers
Serum
Red
Gold
2 mL
Add on stability
This is the length of time after sample collection that this analyte is stable. Test can be added to a previously collected sample if the time since collection is less than the add on stability time.
Minimum Volume
Add On Stability
Collection and Shipping Requirements
Collect at trough (immediately prior to the next infusion); Make at least a 2 mL aliquot of serum; Referred-in sites: freeze aliquots and ship on dry ice to St. Paul’s Hospital. The completed requisition MUST be sent with the specimen.
Reference Intervals
Female Reference Interval
Age Category | Reference Interval | units |
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Male Reference Interval
Age Category | Reference Interval | units |
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Additional Notes
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Measurement Uncertainty (MU)
Every laboratory value is an estimate of the true concentration of substance. MU is the 95% confidence interval around that estimate. 95% of the time, the true concentration will be within the range of the reported value ±MU. This value is based on analytical variability (precision) and does not reflect other factors such as sample collection and handling which may also affect the result.
Example
Reported sodium = 140 mmol/L
Sodium MU = 1%
Expanded uncertainty = 140 mmol/L ± 1% or 140mmol/L ± 1.4 mmol/L
Interpretation - the true value of sodium in the sample is in the range 138.6-141.4 mmol/L, with 95% confidence.
Measurement Uncertainty
Requirements
Specimen collected at trough
Completed requisition: Requisition (issued Sept 2018)
Test ordered and requisition signed by specialist (e.g. gastroenterologist or internist)
Optional
For non-standard collections and special circumstances, complete “Clinical scenario” section of the requisition to expedite test approval, prevent delays in test reporting and facilitate appropriate test interpretation.
Documents
Requisition (issued Sept 2018)
Medical Bulletin - New Methods (issued Aug 2019)
Technical Bulletin for Infusion Sites and Referring-In Labs (issued Aug 2019)