Test Detail
Haemophilus influenzae Isolate Identification/Serotyping
Back to Test DirectoryTest Description |
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This test detects Haemophilus influenzae from isolates. If H. influenzae is detected, serotyping is performed for serotypes A-F. Test performed by the Minnesota Department of Health Public Health Laboratory, St. Paul, MN. | |||||
Performed | Avg. Turnaround Time | Method | |||
Coralville, 8 a.m. - 5 p.m., M-F |
7 - 10 business days | Polymerase Chain Reaction (PCR) | |||
Fee | CPT Code(s) | ||||
No charge | 87149 | ||||
Specimen Requirements | |||||
Specimen Type: | Bacterial isolate specimen | ||||
Collection Instructions: | Actively growing organism in pure culture in a sealed agar plate or slant. Specimen source required. | ||||
Temperature and Stability: | Room Temperature; stable for 72 hours. | ||||
Unacceptable Conditions: | Mixed cultures or non-viable organisms. An additional processing fee will be billed for all mixed cultures. | ||||
Expected Results: | |||||
Haemophilus influenzae Serotype: Final report attached electronically. MDH Sample ID. | |||||
Shipping: | |||||
Wrap specimen container in absorbent material and place inside a biohazard bag. Transport specimen overnight at room temperature. Ship to the Coralville location. | |||||
Comments | |||||
A processing fee will be billed for all organisms submitted that are not in pure culture, as indicated in under Unacceptable Conditions. This test was developed and its performance characteristics determined by the Minnesota Department of Health Public Health Laboratory, 601 North Robert Street, St. Paul, MN 55155 (CLIA Certificate: 24D0651409). It has not been cleared or approved by the US Food and Drug Administration: 21CFR 809.30(e). The FDA has determined that such clearance is not necessary. |