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How reliable are test results from 17 laboratories on the basis of EN 1500 for a hand rub based on 80% (w/w)?
Suchomel, M; Kampf, G; Gebel, J; Droop, F; Christiansen, B; Roesch, K-M.
Afiliación
  • Suchomel M; Institute for Hygiene and Applied Immunology, Medical University of Vienna, Vienna, Austria. Electronic address: miranda.suchomel@meduniwien.ac.at.
  • Kampf G; University Medicine Greifswald, Greifswald, Germany.
  • Gebel J; Institute for Hygiene and Public Health, University Hospital Bonn, Bonn, Germany.
  • Droop F; Institute for Hygiene and Public Health, University Hospital Bonn, Bonn, Germany.
  • Christiansen B; Association for Applied Hygiene, c/o Institute for Hygiene and Public Health, University Hospital Bonn, Bonn, Germany.
  • Roesch KM; Institute for Hygiene and Public Health, University Hospital Bonn, Bonn, Germany.
J Hosp Infect ; 147: 188-196, 2024 May.
Article en En | MEDLINE | ID: mdl-38373530
ABSTRACT

INTRODUCTION:

A ring trial organized by the Association of Applied Hygiene (VAH) on the bactericidal efficacy of an ethanol-based hand rub was carried out in 17 laboratories according to EN 1500 with the aim of describing the variability of test results and fulfilment of the methodological acceptance criteria.

METHOD:

As a test product, a hand rub based on 80% ethanol (w/w) was tested in comparison with the reference alcohol (60% iso-propanol, v/v) in a crossover design. After pre-washing and contamination following the norm, hands were treated either with the reference alcohol (2 × 3 mL for 2 × 30 s) or the test product (3 mL in 30 s). Post-decontamination values were determined immediately after the rub-in period. Validated neutralizers were used. The arithmetic means of all individual log10 pre-values, post-values and reduction values were calculated per laboratory. Non-inferiority was assumed when the Hodges-Lehmann 97.5% confidence limit was <0.6 in comparison with the reference. A z-score was calculated to determine the laboratory performance.

RESULTS:

Two laboratories did not meet the acceptance criteria and were excluded from the analysis. The bactericidal efficacy of the test product was non-inferior to the reference product in four laboratories and not non-inferior in 11 laboratories. The z-score for the Hodges-Lehmann 97.5% confidence limit indicated a satisfactory performance in all laboratories.

CONCLUSION:

We consider the EN 1500 test method to be robust in terms of the variability of test results. For products of borderline efficacy, the evaluation should be based on more than one test.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Desinfección de las Manos / Estudios Cruzados / Etanol Límite: Humans Idioma: En Revista: J Hosp Infect Año: 2024 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Desinfección de las Manos / Estudios Cruzados / Etanol Límite: Humans Idioma: En Revista: J Hosp Infect Año: 2024 Tipo del documento: Article