Coxiella burnetii antibodies (Q-fever)

Which test do we use?

Immunofluorescence test to detect phase I and phase II IgG and IgM antibodies.

 

Due to problems with the immunofluorescence assay, we are temporarily using an ELISA for the determination of C. burnetii phase II IgM antibodies.

Nothing will change in terms of billing.

Sampling instructions

For 1 or 2 serological analyses: at least 1 ml serum
For 3 to 5 serological analyses: at least 2 ml serum

Storage conditions

The serum can be sent at room temperature, but the duration of transportation must be reduced as much as possible (avoid weekends or holidays).

Important advice

Without clinical information and the date of the onset of the symtoms, interpretation of this test is impossible.

Frequence

1-2x / week

Reference values

Negative

Delivery time of the result

On average: 3 days

Accredited

Yes
ISO 15189 – Belac 147-MED

RIZIV-code

551176 / 551180

Loinc-code

fase I IgG:           9708-9

fase II IgG:          9709-7

fase I IgM:          9710-5

fase II IgM:         9711-3

Laatste wijziging op: 26/06/2023