Test Entry - Detail


Q Fever Diagnostic Serology


General
  Clinical Use: Diagnostic testing for Coxiella burnettii infection (Q fever). All specimens are screened with qualitative C. burnettii phase 2 IgG enzyme immunoassay and qualitative IgM indirect fluorescent antibody test (IFA). Specimens with detectable phase 2 IgG have supplementary testing with phase 2 IgG IFA which is reported as a titre. Specimens with a high phase 2 IgG titre have further testing with phase 1 IgG IFA, reported as a titre. Specimens may be referred to Pathology West, NSW, for phase 1 IgA IFA testing if required, provided phase 1 IgG titres are high.
  Availability: Samples are batched and tested twice a week.
  Aliases/Synonyms: Coxiella burnetii Diagnostic Serology ,   Coxiella burnetii Pre-Vaccination Serology,   Q Fever Pre-Vaccination Serology,  
  Code: SEQFV
  Handling Instructions (to laboratory): Send sample chilled.
  Hyperlink:
  Reference Interval:
Refer to report or laboratory


Collection Requirements
  Container: Serum Sep. Tube-SST (GOLD),  
  Sample Type: See container
  Minimum Collection Volume: 3mL
  Collection Instructions:


Processing Requirements
  Alternate Containers:
Serum, no gel (RED)
  Processing Instructions:
  Minimum Assay Volume: 1mL
  Stability: 2 days chilled
  Transport Instructions (to testing laboratory): Send sample chilled.


Testing Locations
  Performed at:
Section Department Site Contact Phone
Serology Microbiology QEII Medical Centre 6383 4427


Last Updated : 07-10-2025 11:59