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Evaluation of the new Vidia® toxoplasmosis IgG and IgM assays in women of childbearing age

Abstract number: 1733_53

Zufferey J., Di Mito C., Auckenthaler R.

Objectives: The aim of the present study was to evaluate the performance of the new VIDIA® Toxoplasmosis IgG and IgM assays (bioMérieux, France), using the VIDIA® system easy to use with a high level of traceability, with clinical specimens prospectively collected in women of childbearing age.

Methods: A total of 1000 fresh serum samples consecutively obtained from 1000 women aged 18–44 years (median 30) during a period of 4 weeks were tested with ADVIA® CentaurTM Toxoplasma IgG and IgM assays according to routine conditions. Serum aliquots stored at + 4°C were blindly rechecked within 24 hours with the VIDIA system for the same parameters. Discrepancies of results between both methods were resolved considering avidity test, direct agglutination (Toxo-Screen DA, bioMérieux), ISAGA (bioMérieux) and when available, the analysis of previous drawn serum samples.

Results: Among the 1000 women screened with VIDIA, 89.4% had non detectable IgG and IgM (T. gondii seronegative) and 8.2% had a pattern of past acquired infection (positive IgG and no detectable IgM). Positive IgM were detected in 1.1% of them with VIDIA system versus 2% with ADVIA Centaur. Equivocal rate was 0.9% for VIDIA TOXO IgG and 0.5% for VIDIA TOXO IgM (versus 0.9% and 1.1%, respectively for the compared method).

For VIDIA TOXO IgG the relative sensitivity and specificity were 96.7% and 99.7%, respectively. After the resolution of discrepancies, the sensitivity as well as the specificity was 100%.

For VIDIA TOXO IgM the initial relative sensitivity and specificity were 64.7% and 100%, respectively. In fact, 4 of the 6 negative samples with VIDIA and positive with the compared method were found with high avidity index and the remaining two samples were negative with the reference test (ISAGA-IgM). Taking this into account, the absolute sensitivity was found 100%.

Conclusion: The two evaluated assays VIDIA TOXO IgG and TOXO IgM have shown an excellent sensitivity and specificity and are well adapted to the routine screening of toxoplasmosis in pregnant women.

Session Details

Date: 31/03/2007
Time: 00:00-00:00
Session name: European Society of Clinical Microbiology and Infectious Diseases
Subject:
Location: ICC, Munich, Germany
Presentation type:
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