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Methicillin-Resistant Staphylococcus aureus (MRSA) Nasal Real-Time PCR: A Predictive Tool for Contamination of the Hospital Environment

Published online by Cambridge University Press:  05 January 2015

Daniel J. Livorsi*
Affiliation:
Richard Roudebush VA Medical Center, Indianapolis, IN Division of Infectious Diseases, Indiana University School of Medicine, Indianapolis, IN
Sana Arif
Affiliation:
Division of Infectious Diseases, Indiana University School of Medicine, Indianapolis, IN
Patricia Garry
Affiliation:
Richard Roudebush VA Medical Center, Indianapolis, IN
Madan G. Kundu
Affiliation:
Indiana University Fairbanks School of Public Health, Department of Biostatistics, Indianapolis, IN
Sarah W. Satola
Affiliation:
Division of Infectious Diseases, Emory University School of Medicine, Atlanta, GA Atlanta VA Medical Center, Decatur, GA
Thomas H. Davis
Affiliation:
Division of Microbiology, Indiana University School of Medicine, Indianapolis, IN
Byron Batteiger
Affiliation:
Richard Roudebush VA Medical Center, Indianapolis, IN Division of Infectious Diseases, Indiana University School of Medicine, Indianapolis, IN
Amy B. Kressel
Affiliation:
Division of Infectious Diseases, Indiana University School of Medicine, Indianapolis, IN
*
Address correspondence to Daniel Livorsi, MD, MSc, Assistant Professor, Division of Infectious Diseases, Indiana University School of Medicine, 545 Barnhill Drive, EH 421 Indianapolis, IN 46202 ([email protected]).

Abstract

OBJECTIVE

We sought to determine whether the bacterial burden in the nares, as determined by the cycle threshold (CT) value from real-time MRSA PCR, is predictive of environmental contamination with MRSA.

METHODS

Patients identified as MRSA nasal carriers per hospital protocol were enrolled within 72 hours of room admission. Patients were excluded if (1) nasal mupirocin or chlorhexidine body wash was used within the past month or (2) an active MRSA infection was suspected. Four environmental sites, 6 body sites and a wound, if present, were cultured with premoistened swabs. All nasal swabs were submitted for both a quantitative culture and real-time PCR (Roche Lightcycler, Indianapolis, IN).

RESULTS

At study enrollment, 82 patients had a positive MRSA-PCR. A negative correlation of moderate strength was observed between the CT value and the number of MRSA colonies in the nares (r=−0.61; P<0.01). Current antibiotic use was associated with lower levels of MRSA nasal colonization (CT value, 30.2 vs 27.7; P<0.01). Patients with concomitant environmental contamination had a higher median log MRSA nares count (3.9 vs 2.5, P=0.01) and lower CT values (28.0 vs 30.2; P<0.01). However, a ROC curve was unable to identify a threshold MRSA nares count that reliably excluded environmental contamination.

CONCLUSIONS

Patients with a higher burden of MRSA in their nares, based on the CT value, were more likely to contaminate their environment with MRSA. However, contamination of the environment cannot be predicted solely by the degree of MRSA nasal colonization.

Type
Original Articles
Copyright
© 2015 by The Society for Healthcare Epidemiology of America. All rights reserved 

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Footnotes

*

Author’s name has been corrected since original publication. An erratum notice detailing this change was also published (DOI 10.1017/ice.2015.10).

References

1.Chaberny, IF, Schwab, F, Ziesing, S, Suerbaum, S, Gastmeier, P. Impact of routine surgical ward and intensive care unit admission surveillance cultures on hospital-wide nosocomial methicillin-resistant Staphylococcus aureus infections in a university hospital: an interrupted time-series analysis. J Antimicrob Chemother 2008;62:14221429.Google Scholar
2.Huang, SS, Yokoe, DS, Hinrichsen, VL, et al. Impact of routine intensive care unit surveillance cultures and resultant barrier precautions on hospital-wide methicillin-resistant Staphylococcus aureus bacteremia. Clin Infect Dis 2006;43:971978.Google Scholar
3.Ellingson, K, Muder, RR, Jain, R, et al. Sustained reduction in the clinical incidence of methicillin-resistant Staphylococcus aureus colonization or infection associated with a multifaceted infection control intervention. Infect Control Hosp Epidemiol 2011;32:18.Google Scholar
4.Robicsek, A, Beaumont, JL, Paule, SM, et al. Universal surveillance for methicillin-resistant Staphylococcus aureus in 3 affiliated hospitals. Ann Intern Med 2008;148:409418.Google Scholar
5.Muder, RR, Cunningham, C, McCray, E, et al. Implementation of an industrial systems-engineering approach to reduce the incidence of methicillin-resistant Staphylococcus aureus infection. Infect Control Hosp Epidemiol. 2008;29:702708; 707 p following 708.Google Scholar
6.Rodriguez-Bano, J, Garcia, L, Ramirez, E, et al. Long-term control of endemic hospital-wide methicillin-resistant Staphylococcus aureus (MRSA): the impact of targeted active surveillance for MRSA in patients and healthcare workers. Infect Control Hosp Epidemiol 2010;31:786795.Google Scholar
7.Jain, R, Kralovic, SM, Evans, ME, et al. Veterans Affairs initiative to prevent methicillin-resistant Staphylococcus aureus infections. N Engl J Med 2011;364:14191430.Google Scholar
8.Boyce, JM, Havill, NL, Kohan, C, Dumigan, DG, Ligi, CE. Do infection control measures work for methicillin-resistant Staphylococcus aureus? Infect Control Hosp Epidemiol 2004;25:395401.Google Scholar
9.Boyce, JM, Potter-Bynoe, G, Chenevert, C, King, T. Environmental contamination due to methicillin-resistant Staphylococcus aureus: possible infection control implications. Infect Control Hosp Epidemiol 1997;18:622627.Google Scholar
10.Baker, SE, Brecher, SM, Robillard, E, Strymish, J, Lawler, E, Gupta, K. Extranasal methicillin-resistant Staphylococcus aureus colonization at admission to an acute care Veterans Affairs hospital. Infect Control Hosp Epidemiol 2010;31:4246.Google Scholar
11.Schechter-Perkins, EM, Mitchell, PM, Murray, KA, Rubin-Smith, JE, Weir, S, Gupta, K. Prevalence and predictors of nasal and extranasal staphylococcal colonization in patients presenting to the emergency department. Ann Emerg Med 2011;57:492499.Google Scholar
12.Shurland, SM, Stine, OC, Venezia, RA, et al. Colonization sites of USA300 methicillin-resistant Staphylococcus aureus in residents of extended care facilities. Infect Control Hosp Epidemiol 2009;30:313318.CrossRefGoogle ScholarPubMed
13.Ridley, M. Perineal carriage of Staph. aureus. Br Med J 1959;1:270273.Google Scholar
14.Rohr, U, Kaminski, A, Wilhelm, M, Jurzik, L, Gatermann, S, Muhr, G. Colonization of patients and contamination of the patients’ environment by MRSA under conditions of single-room isolation. Int J Hyg Environ Health 2009;212:209215.Google Scholar
15.Boyce, JM, Havill, NL, Otter, JA, Adams, NM. Widespread environmental contamination associated with patients with diarrhea and methicillin-resistant Staphylococcus aureus colonization of the gastrointestinal tract. Infect Control Hosp Epidemiol 2007;28:11421147.Google Scholar
16.Morgan, DJ, Rogawski, E, Thom, KA, et al. Transfer of multidrug-resistant bacteria to healthcare workers' gloves and gowns after patient contact increases with environmental contamination. Crit Care Med 2012;40:10451051.Google ScholarPubMed
17.White, A. Relation between quantitative nasal cultures and dissemination of staphylococci. J Lab Clin Med 1961;58:273277.Google ScholarPubMed
18.Chang, S, Sethi, AK, Stiefel, U, Cadnum, JL, Donskey, CJ. Occurrence of skin and environmental contamination with methicillin-resistant Staphylococcus aureus before results of polymerase chain reaction at hospital admission become available. Infect Control Hosp Epidemiol 2010;31:607612.Google Scholar
19. Methicillin-Resistant Staphylococcus Aureus (MRSA) Prevention Initiative. In: Department of Veterans Affairs VHA, ed. Vol VHA directive 2010-006. Washington, DC, 2010.Google Scholar
20.McDougal, LK, Steward, CD, Killgore, GE, Chaitram, JM, McAllister, SK, Tenover, FC. Pulsed-field gel electrophoresis typing of oxacillin-resistant Staphylococcus aureus isolates from the United States: establishing a national database. J Clin Microbiol 2003;41:51135120.Google ScholarPubMed
21.Mermel, LA, Cartony, JM, Covington, P, Maxey, G, Morse, D. Methicillin-resistant Staphylococcus aureus colonization at different body sites: a prospective, quantitative analysis. J Clin Microbiol 2011;49:11191121.Google Scholar
22.Eveillard, M, de Lassence, A, Lancien, E, Barnaud, G, Ricard, JD, Joly-Guillou, ML. Evaluation of a strategy of screening multiple anatomical sites for methicillin-resistant Staphylococcus aureus at admission to a teaching hospital. Infect Control Hosp Epidemiol 2006;27:181184.CrossRefGoogle ScholarPubMed
23.Senn, L, Basset, P, Nahimana, I, Zanetti, G, Blanc, DS. Which anatomical sites should be sampled for screening of methicillin-resistant Staphylococcus aureus carriage by culture or by rapid PCR test? Clin Microbiol Infect 2012;18:E31E33.Google Scholar
24.Matheson, A, Christie, P, Stari, T, et al. Nasal swab screening for methicillin-resistant Staphylococcus aureus—how well does it perform? A cross-sectional study. Infect Control Hosp Epidemiol 2012;33:803808.Google Scholar
25.Yu, VL, Goetz, A, Wagener, M, et al. Staphylococcus aureus nasal carriage and infection in patients on hemodialysis. Efficacy of antibiotic prophylaxis. New Engl J Med 1986;315:9196.Google Scholar
26.McConeghy, KW, Mikolich, DJ, LaPlante, KL. Agents for the decolonization of methicillin-resistant Staphylococcus aureus. Pharmacotherapy 2009;29:263280.Google Scholar
27.Stenehjem, E, Rimland, D, Crispell, EK, Stafford, C, Gaynes, R, Satola, SW. Cepheid Xpert MRSA cycle threshold in discordant colonization results and as a quantitative measure of nasal colonization burden. J Clin Microbiol 2012;50:20792081.Google Scholar
28.Wertheim, HF, Melles, DC, Vos, MC, et al. The role of nasal carriage in Staphylococcus aureus infections. Lancet Infect Dis 2005;5:751762.Google Scholar