ARUP's Laboratory Test Directory

Posaconazole, Quantitation by LC-MS/MS : 2001739
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Additional Technical Information
  


Mnemonic: POSACON AF

Methodology: Quantitative High Performance Liquid Chromatography-Tandem Mass Spectrometry
Performed: Tue, Thu, Sat
Reported: 1-6 days
Specimen Required: Patient Prep: Blood levels may be affected by other concurrent medications, patient conditions, fat intake at dosing, and other factors.

Collect: Plain red, lavender (EDTA), or green (sodium or lithium heparin).

Specimen Preparation: Transfer 1 mL serum to an ARUP Standard Transport Tube and freeze. (Min: 0.6 mL)

Storage/Transport Temperature: Frozen.

Unacceptable Conditions: Serum separator tubes. Hemolyzed or lipemic specimens.

Stability (collection to initiation of testing): After separation from cells: Ambient: 48 hours; Refrigerated: 48 hours; Frozen: 6 months

Reference Interval:
Effective August 15, 2011

Therapeutic Range (trough): Greater than 0.7 µg/mL
Interpretive Data:

See Compliance Statement B: www.aruplab.com/CS
CPT Code(s): 80299
Cross References: Noxafil (Posaconazole, Quantitation by LC-MS/MS), Posanconazole (Posaconazole, Quantitation by LC-MS/MS)