Neutrophil Function, Oxidative Burst

Neutrophil Function, Oxidative Burst

Test Code

37523
86352
37523
86352
In-home collection may be available in your area for purchase through Quest Mobile.

Clinical Significance

Neutrophil Function, Oxidative Burst - This assay measures the capability of neutrophils (PMN) to undergo oxidative metabolism to produce superoxide anion and hydrogen peroxide, as detected by oxidation of dihydrorhodamine (DHR). Patients with chronic granulomatous disease (CGD) are unable to oxidize DHR due to defects in oxidative capacity slowly decreases as the specimen age (hours post collection) increases. It is thus important that the reference range value appropriate for the specimen age be utilized when assessing the reported results.

Test Resources

None found for this test
Please visit our Clinical Education Center to stay informed on any future publications, webinars, or other education opportunities.

Test Details

Methodology

Flow Cytometry (FC)

Assay Category

This test was developed and its analytical performance characteristics have been determined by Quest Diagnostics. It has not been cleared or approved by FDA. This assay has been validated pursuant to the CLIA regulations and is used for clinical purposes.

Reference Range(s)

%Oxidation Pos Neutrophils

24 Hours ≥93%
48 Hours ≥83%
72 Hours ≥82%

LOINC® Codes, Performing Laboratory

Methodology

Flow Cytometry (FC)
This test was developed and its analytical performance characteristics have been determined by Quest Diagnostics. It has not been cleared or approved by FDA. This assay has been validated pursuant to the CLIA regulations and is used for clinical purposes.

Reference Range(s)

%Oxidation Pos Neutrophils
24 Hours ≥93%
48 Hours ≥83%
72 Hours ≥82%

Preferred Specimen(s)

3 mL whole blood collected in a sodium heparin (green-top) tube

Minimum Volume

2 mL

Collection Instructions

Specimen must arrive at the referral laboratory within 72 hours of collection in order to meet sample stability requirements. Specimens are accepted <72 hours post collection. No other preservatives are acceptable. Specify time of day specimen was collected.
Clients may send 4 mL whole blood in sodium heparin from a healthy donor unrelated to the patient, drawn at the same time as the patient sample to run in parallel with the patient's specimen. The outermost label of the tube must be clearly labeled as "Transport Control". If the draw date is not indicated on the specimen, the client must be called and this information obtained.

Clients: Contact the lab prior to ordering for special logistics arrangements.
PSC: Follow short stability Protocol.

Test available by prior arrangement only. Special sample collection and transportation arrangements must be made prior to ordering the test. Contact your local Customer Service Department for specific instructions.

Submit Monday-Thursday only. Do not draw the day before a holiday.
Draw the specimens prior to the last FedEx pick up. Make arrangements with FedEx in advance for same day pick up. Collect and label the specimen(s) according to test requirements. Place the specimen(s) and paperwork into the short stability specimen kit. Use one kit per patient. Use the pre-printed FedEx shipping airbill (provided with the kit) for FedEx Express overnight shipment to Quest Diagnostics Nichols Institute in San Juan Capistrano, CA.

Request Item #170903

Samples received >72 hours after collection will be rejected. Date and time of draw are required and must be provided.

Transport Container

Sodium heparin (green-top) tube

Transport Temperature

Room temperature

Specimen Stability

  • Room temperature: 72 hours
  • Refrigerated: Unacceptable
  • Frozen: Unacceptable

Reject Criteria

Hemolysis • Lipemia • Icterus • Clotted specimens • Received refrigerated • Received frozen

Setup Schedule

3 mL whole blood collected in a sodium heparin (green-top) tube
2 mL
Specimen must arrive at the referral laboratory within 72 hours of collection in order to meet sample stability requirements. Specimens are accepted <72 hours post collection. No other preservatives are acceptable. Specify time of day specimen was collected.
Clients may send 4 mL whole blood in sodium heparin from a healthy donor unrelated to the patient, drawn at the same time as the patient sample to run in parallel with the patient's specimen. The outermost label of the tube must be clearly labeled as "Transport Control". If the draw date is not indicated on the specimen, the client must be called and this information obtained.

Clients: Contact the lab prior to ordering for special logistics arrangements.
PSC: Follow short stability Protocol.

Test available by prior arrangement only. Special sample collection and transportation arrangements must be made prior to ordering the test. Contact your local Customer Service Department for specific instructions.

Submit Monday-Thursday only. Do not draw the day before a holiday.
Draw the specimens prior to the last FedEx pick up. Make arrangements with FedEx in advance for same day pick up. Collect and label the specimen(s) according to test requirements. Place the specimen(s) and paperwork into the short stability specimen kit. Use one kit per patient. Use the pre-printed FedEx shipping airbill (provided with the kit) for FedEx Express overnight shipment to Quest Diagnostics Nichols Institute in San Juan Capistrano, CA.

Request Item #170903

Samples received >72 hours after collection will be rejected. Date and time of draw are required and must be provided.
Sodium heparin (green-top) tube
Room temperature
Room temperature: 72 hours
Refrigerated: Unacceptable
Frozen: Unacceptable
Hemolysis • Lipemia • Icterus • Clotted specimens • Received refrigerated • Received frozen
In-home collection may be available in your area for purchase through Quest Mobile.
Test Details

Clinical Significance

Test Resources

Reference ranges are provided as general guidance only. To interpret test results use the reference range in the laboratory report.

The CPT codes provided are based on AMA guidance and are for informational purposes only. CPT coding is the sole responsibility of the billing party. Please direct any questions regarding coding to the payer being billed.

This material contains content from LOINC® (http://loinc.org). The LOINC Table, LOINC Table Core are copyright © 1995-2019, Regenstrief Institute, Inc. and the Logical Observation Identifiers Names and Codes (LOINC) Committee and is available at no cost under the license at http://loinc.org/license.

The tests listed by specialty and category are a select group of tests offered. For a complete list of Quest Diagnostics tests, please adjust the filter options chosen, or refer to our Directory of Services.