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Ineffectiveness of Hospital Disinfectants Against Bacteria: A Collaborative Study

Published online by Cambridge University Press:  02 January 2015

William A. Rutala*
Affiliation:
Division of Infectious Diseases, Department of Medicine, University of North Carolina, School of Medicine, Chapel Hill Department of Hospital Epidemiology, North Carolina Memorial Hospital, Chapel Hill, North Carolina
Eugene C. Cole
Affiliation:
Division of Infectious Diseases, Department of Medicine, University of North Carolina, School of Medicine, Chapel Hill
*
Division of Infectious Diseases, UNC School of Medicine, 547 Clinical Sciences Bldg. 229H, Chapel Hill, NC 27514

Abstract

A collaborative study was undertaken to assess the degree of variability in disinfectant efficacy test results among laboratories that routinely perform the Association of Official Analytical Chemists (AOAC) Use-Dilution Method. Eighteen laboratories tested identical samples of six EPA-registered, hospital-grade disinfectants (three phenolics and three quaternaries) at the manufacturers' recommended use-dilution using only those modifications of the method approved by the AOAC Use-Dilution Task Force. Each laboratory processed 60 penicylinders for each of the 6 randomly selected disinfectants and 3 test organisms. The current EPA pass criterion for a disinfectant requires a test result of ≤1 positive penicyIinder/60 replicates tested. When compared with the 1 positive/60 replicate criterion, the test results of the 6 disinfectants were: 86 trials (80%) passed and 22 trials (20%) failed against Salmonella choleraesuis ATCC 10708; 71 (66%) passed and 37 (34%) failed against Staphylococcus aureus ATCC 6538; and 41 (38%) passed while 67 (62%) failed against Pseudomonas aeruginosa ATCC 15442. Four laboratories unknowingly tested their own product, and three of the four failed their product against one or more of the test organisms. These results show the inability to reproduce the manufacturers' bactericidal label claims for 6 disinfectants against the 3 AOAC test bacteria. In addition, extreme variability of test results among laboratories testing identical products questions the use of the AOAC Use-Dilution Method for enforcement action.

Type
Original Articles
Copyright
Copyright © The Society for Healthcare Epidemiology of America 1987

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