Pitfalls of rubella serology while on the brink of elimination: evaluation of national data, Belgium, 2017

Author:

Colman Sofie1ORCID,Vernelen Kris2,China Bernard2,Van den Bossche Dorien34,Cornelissen Laura5ORCID,Delforge Marie-Luce64,Reynders Marijke74,Berth Mario84,Depypere Melissa94,Van Gasse Natasja104,Vijgen Sara114,Van Acker Jos124,Boel An41,Padalko Elizaveta134

Affiliation:

1. Clinical Laboratory of Microbiology, OLVZ Aalst, Aalst, Belgium

2. Quality of Laboratories, Sciensano, Brussels, Belgium

3. Institute of Tropical Medicine, Antwerp, Belgium

4. Experts Committee EQA Infectious serology, Quality of Laboratories, Sciensano, Brussels, Belgium

5. Epidemiology of Infectious Diseases, Sciensano, Brussels, Belgium

6. University Hospital Erasme, Brussels, Belgium

7. General Hospital Sint-Jan Bruges, Bruges, Belgium

8. General Hospital AZ Alma, Eeklo, Belgium

9. University Hospital Leuven, Leuven, Belgium

10. Hospital Network Antwerp, Antwerp, Belgium

11. General Hospital Jessa, Hasselt, Belgium

12. General Hospital AZ Sint-Lucas, Ghent, Belgium

13. University Hospital Ghent, Ghent, Belgium

Abstract

Background In Belgium, rubella serology is frequently requested in women of childbearing age, despite high vaccination coverage and a near-absence of congenital rubella cases. Different test kits are available and should be standardised by an international standard preparation. Aim To analyse and compare rubella serology practices in Belgian laboratories. Methods As part of the mandatory External Quality Assessment programme for rubella serology in Belgium, the national public health institute, Sciensano, sent a voluntary questionnaire concerning anti-rubella IgM/IgG analyses in women aged 15 to 45 years in 2017 to 130 laboratories. Results The questionnaire response rate was 83.8% (109/130). The majority of 169,494 IgG analyses were performed on Roche (55%), Abbott (17%) and Diasorin (13%) analysers. Not all laboratories used the proposed international cut-off of 10 IU/mL. Assumed median seroprevalence ranged from 76.3% with Liaison (Diasorin) to 96.3% with Modular (Roche). Despite very low rubella incidence in Belgium, 93 laboratories performed 85,957 IgM analyses, with 748 positive and 394 grey zone results. The National Reference Centre for Measles, Mumps and Rubella virus and the National Reference Centre for Congenital infections did not confirm any positive rubella cases in 2017. Conclusion This retrospective analysis shows that rubella serology results may differ considerably according to the assay used. It is therefore important to use the same test when comparing results or performing follow-up testing. The number of anti-rubella IgM analyses was very high. Incorrect use of IgM for screening women of childbearing age can lead to unwarranted anxiety and overuse of confirmation tests.

Publisher

European Centre for Disease Control and Prevention (ECDC)

Subject

Virology,Public Health, Environmental and Occupational Health,Epidemiology

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