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Methicillin-resistant Staphylococcus aureus (MRSA) screening upon inpatient hospital admission: Is there concordance between nasal swab results and samples taken from skin and soft tissue?

Published online by Cambridge University Press:  12 August 2020

Natasha J. Petry
Affiliation:
Department of Pharmacy Practice, North Dakota State University School of Pharmacy, Fargo, North Dakota
Anna D. Montgomery*
Affiliation:
Fargo Veterans’ Affairs Health Care System, Fargo, North Dakota Department of Public Health, North Dakota State University, Fargo, North Dakota
Kimberly D. P. Hammer
Affiliation:
Fargo Veterans’ Affairs Health Care System, Fargo, North Dakota Department of Internal Medicine, University of North Dakota School of Medicine and Health Sciences, Fargo, North Dakota
Tze Shien Lo
Affiliation:
Fargo Veterans’ Affairs Health Care System, Fargo, North Dakota Department of Internal Medicine, University of North Dakota School of Medicine and Health Sciences, Fargo, North Dakota
*
Author for correspondence: Anna D. Montgomery, E-mail: Anna.montgomery2@va.gov

Abstract

Background:

Methicillin-resistant Staphylococcus aureus (MRSA) infections are associated with increased mortality and healthcare costs. In 2007, a Veterans’ Affairs (VA) hospital implemented a MRSA nasal screening program, following a nationwide VA mandate, in an effort to reduce healthcare-associated MRSA infections.

Objective:

To evaluate the correlation between the nasal screening results for MRSA and culture results of wound and tissue sites.

Methods:

This retrospective study was conducted on inpatients at our VA hospital. Patients were included if they had undergone nasal screening for MRSA plus culture of a wound or tissue site within 30 days of hospital admission.

Results:

In total, 337 patients underwent nasal screening and wound culture and 211 underwent nasal screening and wound and tissue cultures. The prevalence of MRSA nasal colonization was 14.2% for wound samples and 15.2% for tissue samples. The sensitivities of MRSA nasal screening for detecting MRSA were 64.6% for wound cultures and 65.5% for tissue cultures. Specificities were 86.2% and 88.8% for wound and tissue cultures, respectively. The positive predictive values (PPVs) were 43.7% and 51.2% for wound and tissue cultures, respectively, and the negative predictive values (NPVs) were high at 93.6% and 93.5%, respectively.

Conclusions:

In cases of wound or tissue samples for which culture results are pending, a negative MRSA nasal swab may be a component of the decision to withhold or discontinue MRSA-active agents.

Type
Original Article
Copyright
© 2020 by The Society for Healthcare Epidemiology of America. All rights reserved.

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References

Keene, A, Vavagiakis, P, Lee, MH, et al. Staphylococcus aureus colonization and the risk of infection in critically ill patients. Infect Control Hosp Edidemiol 2005;26:622628.10.1086/502591CrossRefGoogle ScholarPubMed
Peterson, LR, Boehm, S, Beaumont, JL, et al. Reduction of methicillin-resistant Staphylococcus aureus infection in long-term care is possible while maintaining patient socialization: a prospective randomized clinical trial. Am J Infect Control 2016;44:16221627.10.1016/j.ajic.2016.04.251CrossRefGoogle ScholarPubMed
Marshall, C, Richards, M, Mcbryde, E. Do active surveillance and contact precautions reduce MRSA acquisition? A prospective interrupted time series. PLoS One 2013;8(3):e58112.10.1371/journal.pone.0058112CrossRefGoogle ScholarPubMed
Dantes, R, Mu, Y, Belflower, R. National burden of invasive methicillin-resistant Staphylococcus aureus infections, United States, 2011. JAMA Intern Med 2013;173:19701978.Google ScholarPubMed
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;49:11191121.10.1128/JCM.02601-10CrossRefGoogle ScholarPubMed
Jarvis, WR, Jarvis, AA, Chinn, RY. National prevalence of methicillin-resistant Staphylococcus aureus in inpatients at United States healthcare facilities, 2010. Am J Infect Control 2012;40:194200.10.1016/j.ajic.2012.02.001CrossRefGoogle Scholar
Bisaga, A, Paquette, K, Sabatini, L, Lovell, EO. A prevalence study of methicillin-resistant Staphylococcus aureus colonization in emergency department healthcare workers. Ann Emerg Med 2008;52:525.10.1016/j.annemergmed.2008.03.019CrossRefGoogle Scholar
Suffoletto, BP, Cannon, EH, Ilkhanipour, K, Yealy, DM. Prevalence of Staphylococcus aureus nasal colonization in emergency department personnel. Ann Emerg Med 2008;52:529.10.1016/j.annemergmed.2008.03.020CrossRefGoogle ScholarPubMed
Davis, KA, Stewart, JJ, Crouch, HK, Florez, CE, Hospenthal, DR. Methicillin-resistant Staphylococcus aureus (MRSA) nares colonization at hospital admission and its effect on subsequent MRSA infection. Clin Infect Dis 2004;39:776782.10.1086/422997CrossRefGoogle ScholarPubMed
Jinadatha, C, Hussain, Z, Erickson, TA, Villamaria, FC, Copeland, LA, Huber, TW. Origin of methicillin-resistant Staphylococcus aureus healthcare-associated infections: evaluation of the role of anterior nares. Am J Inf Con 2015;43:11251127.10.1016/j.ajic.2015.05.026CrossRefGoogle ScholarPubMed
Jain, R, Kralovic, SM, Evans, ME, et al. Veterans’ Affairs initiative to prevent methicillin-resistant Staphylococcus aureus infections. N Engl J Med 2011;364:14191430.10.1056/NEJMoa1007474CrossRefGoogle Scholar
Radigan, K. Nasal screening for MRSA: the new basis for de-escalation of empiric antibiotics? Critical Care Alert 2015;23:34.Google Scholar
Tilahun, B, Faust, AC, McCorstin, P, Ortegon, A. Nasal colonization and lower respiratory tract infections with methicillin-resistant Staphylococcus aureus . Am J Crit Care 2015;24:812.10.4037/ajcc2015102CrossRefGoogle ScholarPubMed
Dangerfield, B, Chung, A, Webb, B, Seville, MT. Predictive value of methicillin-resistant Staphylococcus aureus (MRSA) nasal swab PCR assay for MRSA pneumonia. Antimicrob Agents Chemother 2014;58:859864.10.1128/AAC.01805-13CrossRefGoogle ScholarPubMed
Hiett, J, Patel, RK, Tate, V, Smulian, G, Kelly, A. Using active methicillin-resistant Staphylococcus aureus surveillance nasal swabs to predict clinical respiratory culture results. Am J Health Syst Pharm 2015;72(11 suppl 1): S20S24.10.2146/ajhp140820CrossRefGoogle ScholarPubMed
Lachenbruch, PA. McNemar Test. Wiley StatsRef: Statistics Reference Online. 2014. doi: 10.1002/9781118445112.CrossRefGoogle Scholar
Donovan, TM, Bayes’ Theorem, Mickey RM.. Bayesian Statist 2019:2936.10.1093/oso/9780198841296.003.0003CrossRefGoogle Scholar
MRSA screening. American Association of Clinical Chemistry website. http://labtestsonline.org/tests/mrsa-screening. Updated December 6, 2006. Accessed June 17, 2020.Google Scholar
Johnson, JA, Wright, ME, Sheperd, LA, Musher, DM, Dang, BN. Nasal methicillin-resistant Staphylococcus aureus polymerase chain reaction: a potential use in guiding antibiotic therapy for pneumonia. Perm J 2015;19:3436.10.7812/TPP/14-101CrossRefGoogle ScholarPubMed
Robicsek, A, Suseno, M, Beaumont, JL, Thomson, RB Jr, Peterson, LR. Prediction of methicillin-resistant Staphylococcus aureus involvement in disease sites by concomitant nasal sampling. J Clin Microbiol 2008;46:588592.10.1128/JCM.01746-07CrossRefGoogle ScholarPubMed
Gunderson, CG, Holleck, JL, Chang, JJ, Merchant, N, Lin, S, Gupta, S. Diagnostic accuracy of methicillin-resistant Staphylococcus aureus nasal colonization to predict methicillin-resistant S aureus soft-tissue infections. Am J Infect Control 2016;44:11761177.10.1016/j.ajic.2016.03.039CrossRefGoogle ScholarPubMed