The Journal of hospital infection
October 1, 2026 · via Europe PMC
Efficacy of 'sporicidal' ready-to-use disinfectant wipes against Clostridioides difficile: comparison of standard and modified EN 17846 wiping procedures.
Rausch M, Berreßem B, Mosel KM, +11 more, Gebel J.
AI summary — for doctors, generated from the abstract only
Not all 'sporicidal' wipes pass C. difficile efficacy testing; those confirmed in two labs passed both suspension and surface tests.
What was studied
Laboratory evaluation of five wipes using EN 17126 and EN 17846, with standard and modified wiping.
Key findings
- Products confirmed in two labs met criteria in both tests
- Some products without confirmation showed activity while others failed
- Wiping trajectory was compared
Clinical relevance
Product claims should be checked against independent data.
Who should care
Limitations
Lab study; abstract truncated.
Choose wipes with independently confirmed sporicidal activity.
This is an AI-generated summary of the published abstract, not a clinical recommendation. It may not reflect the full text or subsequent updates — verify against the original source before acting on it.
Abstract
Background
Sporicidal surface disinfection is essential for preventing the transmission of Clostridioides difficile in healthcare settings. However, not all products with marketed sporicidal claims have demonstrated consistent efficacy. Standardized evaluation of sporicidal efficacy is based on both quantitative suspension testing (EN 17126) and the practice-oriented 4-field surface test with mechanical action (EN 17846). While these methods are well established, methodological aspects related to wiping trajectories are under discussion.
Methods
Five ready-to-use disinfectant wipes with sporicidal claims were evaluated against C. difficile spores using EN 17126 suspension tests and EN 17846 4-field surface tests. In the surface test, both the standard wiping trajectory and a modified linear wiping procedure were applied.
Results
Products with sporicidal efficacy confirmed in two independent laboratories fulfilled the efficacy criteria in both suspension and surface tests. Among products without such confirmation, sporicidal activity was observed, whereas others failed to meet efficacy requirements. The modified wiping procedure resulted in lower reductions on the primary field and increased transfer to secondary fields in the water control. While products with clearly effective or ineffective profiles were not meaningfully affected, borderline-performing products showed reduced efficacy under the modified procedure.
Conclusion
Comparative evaluation under standard and modified EN 17846 conditions demonstrated that increased methodological stringency affects the results of borderline-performing products, while clearly effective products remain consistently effective. These findings indicate that wiping trajectory is a relevant methodological parameter in EN 17846 testing, particularly for products performing close to the efficacy threshold.
DOI
10.1016/j.jhin.2026.09.024
PMID
42822780
Research metadata (titles, abstracts, authors, publication dates) is sourced from Europe PMC, which aggregates content from PubMed/MEDLINE, PubMed Central, and other providers under the U.S. National Library of Medicine (NLM/NCBI). NLM does not claim copyright on abstracts; the original journal publishers or authors may hold rights to the full articles. AI-generated summaries are derived only from the abstract, never the full text, and are always labeled as AI-generated.
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