Neutrophil Oxidative Burst, Blood




Test Mnemonic

OXBRST

CPT Codes

  • 86352 - QTY (1)

Performing Laboratory

ARUP


Specimen Requirements

Volume Type Container Collect Temperature Transport Temperature Special Instructions
3 mLWhole bloodSodium or Lithium heparin (Green) See noteCRITICAL AMBIENT. THIS TEST REQUIRES MULTIPLE SPECIMENS. Send both specimens to Cleveland Clinic Laboratories on the day of collection by 3 p.m. EST.
3 mLWhole bloodSodium or Lithium heparin (Green) See noteCRITICAL AMBIENT. THIS TEST REQUIRES MULTIPLE SPECIMENS. Collect this specimen from an unrelated healthy person; label the tube as "Control." Both tubes must be received in Cleveland Clinic Laboratories on the day of collection by 3 p.m. EST. Patient and control specimens must be collected within 48 hours of test performance. Do NOT refrigerate or freeze as live neutrophils are required.

Minimum Specimen Requirements

Volume Type Container Collect Temperature Transport Temperature Special Instructions
Other    Note: Minimum volume is 1 mL per tube (patient and control). Prefer 3 mL per tube.

Stability

Environmental Condition Description
Ambient48 hours
FrozenUnacceptable
RefrigeratedUnacceptable

Days Performed

Sun - Sat

Turnaround Time

3 - 4 days

Methodology

Name Description
Semi-Quantiative Flow Cytometry 

Reference Range

Special Info

CRITICAL AMBIENT. Patient prep: Collect control specimen from a healthy individual unrelated to patient at approximately the same time as and under similar conditions to the patient. Patient and control specimens MUST be collected within 48 hours of test performance. Do NOT refrigerate or freeze as live neutrophils are required. Ambient stability is 24 hours for New York clients. This test is New York DOH approved.

Clinical Info

Aids in screening for chronic granulomatous disease. White blood cells are incubated with dihydrorhodamine 123 (DHR) and catalase, then stimulated with Phorbol 12-Myristate 13-Acetate (PMA). Dihydrorhodamine oxidation to rhodamine by the respiratory burst of the cell is measured by flow cytometry. Results are reported as the ratio of the mean channel fluorescence of stimulated cells versus unstimulated cells, which yields a stimulation index (SI). If sample shows abnormal results when stimulated, and no control was sent, test should be resubmitted with control sample to validate the conditions of collection, processing and transport. Interpretation comparing the patient results to the client normal control and the laboratory control will be provided by the medical director.