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Test Order

Haemophilus influenzae
Identification/Confirmation/Serotyping

Pre-Approval Required

None

Supplemental Information or Form

1.    Pure, viable subculture of an isolate from a sterile body source

2.    Completed submittal form with 2 patient identifiers (e.g. name and date of birth), collection date and source, a brief but complete patient history, cultural history and submitting laboratory’s findings

3.    Documentation that indicates the role of this isolate in clinical disease

Performed on Specimens from

None

Acceptable Sample/Specimen Type for Testing

Confirmed or suspected Haemophilus influenzae isolate

Minimum Volume Required

None

Storage & Preservation of Specimen Prior to Shipping

None

Transport Medium

Tubed chocolate agar medium with a secure screw cap, labeled with patient’s name

Specimen Labeling

None

Shipping Instructions which Include Specimen Handling Requirements

1.    Grow isolate under appropriate conditions prior to shipping.

2.    Ship at ambient temperature using appropriate DOT/IATA approved shipping procedures.

Test Methodology

As needed - Biochemical testing, Serotyping by slide agglutination, Gene Sequencing by PCR, and/ or MALDI-TOF mass spectrometry. Please note that serotyping will only be performed on isolates from sterile body sites, such as blood or cerebrospinal fluid that are confirmed as Haemophilus influenzae.

Turnaround Time

1 week

Interferences & Limitations

Mixed or nonviable culture

Additional Information

Please contact the MDL Special Pathogens Unit for special consideration if any of the above criteria cannot be met.

MDL Points of Contact

Special Pathogens Unit (510) 412-3903

Monday-Friday 8 AM to 5 PM PT

Emails: margot.graves@cdph.ca.gov or robin.hogue@cdph.ca.gov

 
 
Last modified on: 10/8/2013 11:15 AM