Last updated on 28-2-2025 by Amber Van Laer
Description of tests
- RNA of rubella virus is detected by real-time PCR on amniotic fluid.
- The sensitivity of this PCR for the diagnosis of congenital Rubella is estimated to be 90%.
Purpose of testing
To detect Rubella virus on amniotic fluid in a pregnant woman to diagnose possible congenital Rubella infection in the foetus.
Criteria for performing this test
- The reference centre performs PCR on amniotic fluid from pregnant patients at risk of congenital Rubella.
- Application forms must be completed in full.
Instructions for samples and transport
Amniotic fluid: 2 ml, stored at 4°C; ship at room temperature no later than the day after collection.
Unacceptable requests
- Incomplete request form
- Sample not suitable for analysis
- Incorrect transport/storage.
Turn around time
Response time: 1 to 5 working days (contact the laboratory in case of emergency)
Reporting of test results
The laboratory reports the results and comments and sends it to the requesting laboratory by post or fax.
Accreditation
Is the analysis accredited?
Materials and methods
Material(s):
Method reference:
-
Turnaround time and time slots
Turnaround time:
7 days
Request forms
Analysis categories
Medical
