Key result
Standardizing serological outcomes across different laboratories and assays altered seroprevalence estimates by an average of 3.2%, with differences up to 16% for specific antigens like hepatitis A.
Observational
Yes
Standardization of serological outcomes across different laboratories and assays is necessary, as crude estimates can differ significantly (up to 16%) compared to standardized estimates.
Answers are grounded in this paper and cite their sources.
May warrant assay standardization in multi-country serosurveys to limit up to 16% estimate shifts; leaves open effects on vaccination policy.
The aim of the European Sero-Epidemiology Network 2 (ESEN2) project was to estimate age-specific seroprevalence for a number of vaccine-preventable diseases in Europe. To achieve this serosurveys were collected by 22 national laboratories. To adjust for a variety of laboratory methods and assays, all quantitative results were transformed to a reference laboratory's units and were then classified as positive or negative to obtain age-specific seroprevalence. The aim of this study was to assess the value of standardization by comparing the crude and standardized seroprevalence estimates. Seroprevalence was estimated for measles, mumps, rubella, diphtheria, varicella zoster and hepatitis A virus (HAV) and compared before and after serological results had been standardized. The results showed that if no such adjustment had taken place, seroprevalence would have differed by an average of 3·2% (95% bootstrap interval 2·9-3·6) although this percentage varied substantially by antigen. These differences were as high as 16% for some serosurveys (HAV) which means that standardization could have a considerable impact on seroprevalence estimates and should be considered when comparing serosurveys performed in different laboratories using different assay methods.
No takes yet. Share an insight, caveat, or question.
Kafatos et al. (2014) conducted an observational in Vaccine-preventable infections (measles, mumps, rubella, diphtheria, varicella zoster, hepatitis A). Standardization of serological outcomes vs. Crude (non-standardized) seroprevalence estimates was evaluated on Mean seroprevalence difference before and after standardization (3.2%, 95% CI 2.9-3.6). Standardizing serological outcomes across different laboratories and assays altered seroprevalence estimates by an average of 3.2%, with differences up to 16% for specific antigens like hepatitis A.
Synapse has enriched 10 related papers. Consider them for comparative context: