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Reply to Widmer and Tschudin-Sutter

Published online by Cambridge University Press:  22 April 2015

Venkata C. K. Sunkesula
Affiliation:
Division of Infectious Diseases, Department of Medicine, Case Western Reserve University School of Medicine, Cleveland, Ohio
Sirisha Kundrapu
Affiliation:
Division of Infectious Diseases, Department of Medicine, Case Western Reserve University School of Medicine, Cleveland, Ohio
David R. Macinga
Affiliation:
Research and Development, GOJO Industries, Akron, Ohio Department of Integrative Medical Sciences, Northeastern Ohio Medical University, Rootstown, Ohio
Curtis J. Donskey*
Affiliation:
Division of Infectious Diseases, Department of Medicine, Case Western Reserve University School of Medicine, Cleveland, Ohio Geriatric Research, Education, and Clinical Center, Cleveland Veterans Affairs Medical Center, Cleveland, Ohio.
*
Address correspondence to Curtis J. Donskey, MD, Geriatric Research, Education, and Clinical Center, Cleveland Veterans Affairs Medical Center, 10701 East Blvd, Cleveland, Ohio 44106 (curtisd123@yahoo.com).
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Abstract

Type
Letters to the Editor
Copyright
© 2015 by The Society for Healthcare Epidemiology of America. All rights reserved 

To the Editor—We appreciate the interest in our recent articleReference Sunkesula, Kundrapu, Macinga and Donskey 1 and would like to respond to issues raised by Widmer and Tschudin-SutterReference Widmer and Tschudin-Sutter 2 as possible explanations why 2 mL of a 70% alcohol handrub product did not completely eradicate methicillin-resistant Staphylococcus aureus (MRSA) from the hands of colonized patients. First, the assertion that the handrub used in the study did not meet the European Standards (EN 1500) requirements within 30 seconds of application is inaccurate. Although a product of the same brand name was evaluated by Kramer et al,Reference Kramer, Rudolph, Kampf and Pittet 3 that was a previous formulation based on 62% (vol/vol) ethanol. The product used in the current study is based on 70% (vol/vol) ethanol and meets both the EN 1500 efficacy requirements within 30 seconds and the US Food and Drug Administration Healthcare Personnel Handwash requirements at a 2 mL application.Reference Edmonds, Macinga and Mays-Suko 4 Therefore incomplete MRSA eradication cannot be attributed to a lack of efficacy of the handrub product. Second, we acknowledge that a larger volume of product may have been more effective because handrub efficacy is highly dependent on application volume. Further studies to investigate the impact of product volume on clinical efficacy are warranted. We point out, however, that there is a practical limit to the volume of product end users will apply, which is largely influenced by dry-time. The volume of handrub used in this study (2 mL) takes approximately 30 seconds to rub dry and is consistent with World Health Organization recommendations; in contrast, a volume of 3 mL typically remains wet longer than 30 seconds and can take as long as 90 seconds to dry on hands.Reference Macinga, Shumaker and Werner 5 Third, as stated in our article, patients were asked to rub their hands for 30 seconds with coaching to ensure proper technique according to World Health Organization recommendations. A majority of participants studied were elderly and some displayed diminished hand dexterity, which may have impacted our results. However, there is still debate whether the 6-step technique outlined by the World Health Organization provides an efficacy benefit.Reference Kampf, Reichel, Feil, Eggerstedt and Kaulfers 6 , Reference Widmer and Dangel 7 We agree that the ability of handrub products to meet established efficacy requirements, as well as product application volume and good technique to ensure adequate hand coverage, are all important variables that influence clinical efficacy. However, we caution against the generalization of the results obtained with this specific population of MRSA-colonized patients to make predictions on the ability of alcohol handrub products to eliminate transient MRSA from the hands of healthcare workers.

Acknowledgments

Financial support. Department of Veterans Affairs.

Potential conflicts of interest. C.J.D. reports that he has received research grants from Steris, Pfizer, 3M, Clorox, and GOJO, and has served on scientific advisory boards for 3M and Merck. D.R.M. reports that he is an employee of GOJO. All other authors report no conflicts of interest relevant to this article.

References

1. Sunkesula, V, Kundrapu, S, Macinga, DR, Donskey, CJ. Efficacy of alcohol gel for removal of methicillin-resistant Staphylococcus aureus from hands of colonized patients. Infect Control Hosp Epidemiol 2015;36:229231.Google Scholar
2. Widmer, AF, Tschudin-Sutter, S. Letter to the editor regarding “Efficacy of alcohol gel for removal of methicillin-resistant Staphylococcus aureus from hands of colonized patients.” Infect Control Hosp Epidemiol 2015; doi:10.1017/ice.2015.94.Google Scholar
3. Kramer, A, Rudolph, P, Kampf, G, Pittet, D. Limited efficacy of alcohol-based hand gels. Lancet 2002;359:14891490.Google Scholar
4. Edmonds, SL, Macinga, DR, Mays-Suko, P, et al. Comparative efficacy of commercially available alcohol-based hand rubs and WHO-recommended hand rubs: formulation matters. Am J Infect Control 2012;40:521525.Google Scholar
5. Macinga, DR, Shumaker, DJ, Werner, H-P, et al. The relative influences of product volume, delivery format and alcohol concentration on dry-time and efficacy of alcohol-based hand rubs. BMC Infect Dis 2014;14:511.Google Scholar
6. Kampf, G, Reichel, M, Feil, Y, Eggerstedt, S, Kaulfers, PM. Influence of rub-in technique on required application time and hand coverage in hygienic hand disinfection. BMC Infect Dis 2008;8:149.Google Scholar
7. Widmer, AE, Dangel, M. Alcohol-based handrub: evaluation of technique and microbiological efficacy with international infection control professionals. Infect Control Hosp Epidemiol 2004;25:207209.Google Scholar