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Methicillin-Resistant Staphylococcus aureus: Site of Acquisition and Strain Variation in High-Risk Nursing Home Residents with Indwelling Devices

Published online by Cambridge University Press:  10 May 2016

Kristen E. Gibson
Affiliation:
University of Michigan School of Public Health, Ann Arbor, Michigan
Sara E. McNamara
Affiliation:
Division of Geriatric and Palliative Care Medicine, University of Michigan Medical School, Ann Arbor, Michigan
Marco Cassone
Affiliation:
Division of Geriatric and Palliative Care Medicine, University of Michigan Medical School, Ann Arbor, Michigan
Mary Beth Perri
Affiliation:
Henry Ford Health System, Detroit, Michigan
Marcus Zervos
Affiliation:
Henry Ford Health System, Detroit, Michigan Wayne State University School of Medicine, Detroit, Michigan
Lona Mody*
Affiliation:
Division of Geriatric and Palliative Care Medicine, University of Michigan Medical School, Ann Arbor, Michigan Geriatrics Research Education and Clinical Center, Veterans Affairs Ann Arbor Healthcare System, Ann Arbor, Michigan
on behalf of the Targeted Infection Prevention (TIP) Study Team, Ann Arbor, Michigan
Affiliation:
Geriatrics Research Education and Clinical Center, Veterans Affairs Ann Arbor Healthcare System, Ann Arbor, Michigan
*
University of Michigan Medical School Division of Geriatric and Palliative Care Medicine, 300 North Ingalls Road, Room 905, Ann Arbor, MI 48109 (lonamody@.umich.edu).

Abstract

Objective.

Characterize the clinical and molecular epidemiology of new methicillin-resistant Staphylococcus aureus (MRSA) acquisitions at nasal and extranasal sites among high-risk nursing home (NH) residents.

Design.

Multicenter prospective observational study.

Setting.

Six NHs in southeast Michigan.

Participants.

A total of 120 NH residents with an indwelling device (feeding tube and/or urinary catheter).

Methods.

Active surveillance cultures from the nares, oropharynx, groin, perianal area, wounds (if present), and device insertion site(s) were collected upon enrollment, at day 14, and monthly thereafter. Pulsed-field gel electrophoresis and polymerase chain reaction for SCCmec, agr, and Panton-Valentine leukocidin were performed.

Results.

Of 120 participants observed for 16,290 device-days, 50 acquired MRSA (78% transiently, 22% persistently). New MRSA acquisitions were common in extranasal sites, particularly at device insertion, groin, and perianal areas (27%, 23%, and 17.6% of all acquisitions, respectively). Screening extranasal sites greatly increases the detection of MRSA colonization (100% of persistent carriers and 97.4% of transient carriers detected with nares, groin, perianal, and device site sampling vs 54.5% and 25.6%, respectively, for nares samples alone). Colonization at suprapubic urinary catheter sites generally persisted. Healthcare-associated MRSA (USA100 and USA100 variants) were the dominant strains (79.3% of all new acquisition isolates). Strain diversity was more common in transient carriers, including acquisition of USA500 and USA300 strains.

Conclusion.

Indwelling device insertion sites as well as the groin and perianal area are important sites of new MRSA acquisitions in NH residents and play a role in the persistency of MRSA carriage. Clonal types differ among persistent and transient colonizers.

Type
Original Article
Copyright
© 2014 by The Society for Healthcare Epidemiology of America. All rights reserved.

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References

1. Centers for Medicare and Medicaid Services. Nursing Home Data Compendium 2012. http://www.cms.gov/Medicare/Provider-Enrollment-and-Certification/CertificationandComplianc/downloads/nursinghomedatacompendium_508.pdf. Accessed September 10, 2013.Google Scholar
2. Bradley, SF, Terpenning, MS, Ramsey, MA, et al. Methicillin-resistant Staphylococcus aureus: colonization and infection in a long-term care facility. Ann Intern Med 1991;115:417422.Google Scholar
3. O’Sullivan, NP, Keane, CT. Risk factors for colonization with methicillin-resistant Staphylococcus aureus among nursing home residents. J Hosp Infect 2000;45:206210.Google Scholar
4. Muder, RR, Brennen, C, Wagener, MM, et al. Methicillin-resistant staphylococcal colonization and infection in a long-term care facility. Ann Intern Med 1991;114:107112.Google Scholar
5. Mody, L, Maheshwari, S, Galecki, A, Kauffman, CA, Bradley, SF. Indwelling device use and antibiotic resistance in nursing homes: identifying a high-risk group. J Am Geriatr Soc 2007;55:19211926.CrossRefGoogle ScholarPubMed
6. Dommeti, P, Wang, L, Flannery, EL, Symons, K, Mody, L. Patterns of ciprofloxacin-resistant gram-negative bacteria colonization in nursing home residents. Infect Control Hosp Epidemiol 2011;32:177180.Google Scholar
7. Kluytmans, J, van Belkum, A, Verbrugh, H. Nasal carriage of Staphylococcus aureus: epidemiology, underlying mechanisms, and associated risks. Clin Microbiol Rev 1997;10:505520.Google Scholar
8. Vandenbergh, MF, Yzerman, EP, van Belkum, A, et al. Follow-up of Staphylococcus aureus nasal carriage after 8 years: redefining the persistent carrier state. J Clin Microbiol 1999;37:31333140.Google Scholar
9. Mody, L, Bradley, SF, Galecki, A, et al. Conceptual model for reducing infections and antimicrobial resistance in skilled nursing facilities: focusing on residents with indwelling devices. Clin Infect Dis 2011;52:654661.CrossRefGoogle ScholarPubMed
10. 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 Scholar
11. Lina, G, Piemont, Y, Godail-Gamot, F, et al. Involvement of Panton-Valentine leukocidin-producing Staphylococcus aureus in primary skin infections and pneumonia. Clin Infect Dis 1999;29:11281132.Google Scholar
12. Okuma, K, Iwakawa, K, Turnidge, JD, et al. Dissemination of new methicillin-resistant Staphylococcus aureus clones in the community. J Clin Microbiol 2002;40:42894294.Google Scholar
13. Kondo, Y, Ito, T, Ma, XX, et al. Combination of multiplex PCRs for staphylococcal cassette chromosome mec type assignment: rapid identification system for mec, ccr, and major differences in junkyard regions. Antimicrob Agents Chemother 2007;51:264274.Google Scholar
14. Witte, W, Enright, M, Schmitz, FJ, Cuny, C, Braulke, C, Heuck, D. Characteristics of a new epidemic MRSA in Germany ancestral to United Kingdom EMRSA 15. Int J Med Microbiol 2001;290:677682.Google Scholar
15. Strommenger, B, Cuny, C, Werner, G, Witte, W. Obvious lack of association between dynamics of epidemic methicillin-resistant Staphylococcus aureus in Central Europe and agr specificity groups. Eur J Clin Microbiol Infect Dis 2004;23:1519.Google Scholar
16. Zhang, K, McClure, J, Elsayed, S, Louie, T, Conly, JM. Novel multiplex PCR assay for characterization and concomitant subtyping of staphylococcal cassette chromosome mec types I to V in methicillin-resistant Staphylococcus aureus. J Clin Microbiol 2005;43:50265033.Google Scholar
17. Tenover, FC, McDougal, LK, Goering, RV, et al. Characterization of a strain of community-associated methicillin-resistant Staphylococcus aureus widely disseminated in the United States. J Clin Microbiol 2006;44:108111.Google Scholar
18. Cohen, AL, Calfee, D, Fridkin, SK, et al. Recommendations for metrics for multidrug-resistant organisms in healthcare settings: SHEA/HICPAC position paper. Infect Control Hosp Epidemiol 2008;29:901913.Google Scholar
19. Martinez-Capolino, C, Reyes, K, Johnson, L, et al. Impact of active surveillance on meticillin-resistant Staphylococcus aureus transmission and hospital resource utilization. J Hosp Infect 2010;74:232237.Google Scholar
20. Wang, L, Lansing, B, Symons, K, et al. Infection rate and colonization with antibiotic-resistant organisms in skilled nursing facility residents with indwelling devices. Eur J Clin Microbiol Infect Dis 2012;31(8):17971804.Google Scholar
21. Fisch, J, Lansing, B, Wang, L, et al. New acquisitions of antibiotic-resistant organisms in skilled nursing facilities. J Clin Microbiol 2012;50(5):16981703.Google Scholar
22. Kluytmans, JA, Wertheim, HF. Nasal carriage of Staphylococcus aureus and prevention of nosocomial infections. Infection 2005;33:38.Google Scholar
23. McKinnell, JA, Huang, SS, Eells, SJ, Cui, E, Miller, LG. Quantifying the impact of extra-nasal testing body sites for MRSA colonization at the time of hospital or intensive care unit admission. Infect Control Hosp Epidemiol 2013;34:161170.CrossRefGoogle ScholarPubMed
24. Mody, L, Kauffman, CA, Donabedian, S, Zervos, M, Bradley, SF. Patterns of nasal and extra-nasal colonization with S. aureus in nursing homes. Clin Infect Dis 2008;46:13681373.Google Scholar
25. Nouwen, J, Boelens, H, van Belkum, A, Verbrugh, H. Human factor in Staphylococcus aureus nasal carriage. Infect Immun 2004;72:66856688.Google Scholar
26. Nouwen, JL, Ott, A, Kluytmans-Vandenbergh, MF, et al. Predicting the Staphylococcus aureus nasal carrier state: derivation and validation of a “culture rule.” Clin Infect Dis 2004;39:806811.Google Scholar
27. Hudson, LO, Reynolds, C, Spratt, BG, et al. Diversity of methicillin-resistant Staphylococcus aureus strains isolated from residents of 26 nursing homes in Orange County, California. J Clin Microbiol 2013;51:37883795.Google Scholar
28. Yang, ES, Tan, J, Eells, S, Rieg, G, Tagudar, G, Miller, LG. Body site colonization in patients with community-associated methicillin-resistant Staphylococcus aureus and other types of S. aureus skin infections. Clin Microbiol Infect 2010;16:425431.Google Scholar
29. Stone, ND, Lewis, DR, Lowery, HK, et al. Importance of bacterial burden among methicillin-resistant Staphylococcus aureus carriers in a long-term care facility. Infect Control Hosp Epidemiol 2008;29:143148.Google Scholar
30. Lederer, SR, Riedelsdorf, G, Schiffl, H. Nasal carriage of methicillin-resistant Staphylococcus aureus: the prevalence, patients at risk and the effect of elimination on outcomes among outclinic haemodialysis patients. Eur J Med Res 2007;12:284288.Google Scholar
31. Stone, ND, Lewis, DR, Johnson, TM, et al. Methicillin-resistant Staphylococcus aureus (MRSA) nasal carriage in residents of Veterans Affairs long-term care facilities: role of antimicrobial exposure and MRSA acquisition. Infect Control Hosp Epidemiol 2012;33:551557.Google Scholar