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Use of a cohorting-unit and systematic surveillance cultures to control a Klebsiella pneumoniae carbapenemase (KPC)–producing Enterobacteriaceae outbreak

Published online by Cambridge University Press:  14 May 2019

Allison E. Reeme
Affiliation:
Department of Infection Prevention and Control, Froedtert Memorial Lutheran Hospital, Milwaukee, Wisconsin
Sarah L. Bowler
Affiliation:
Division of Infectious Diseases, University of Pittsburgh, Pittsburgh, Pennsylvania
Blake W. Buchan
Affiliation:
Department of Pathology, Medical College of Wisconsin, Milwaukee, Wisconsin
Mary Beth Graham
Affiliation:
Division of Infectious Diseases, Department of Medicine, Medical College of Wisconsin, Milwaukee, Wisconsin
Elizabeth Behrens
Affiliation:
Froedtert Memorial Lutheran Hospital, Milwaukee, Wisconsin
Siddhartha Singh
Affiliation:
Division of General Medicine, Medical College of Wisconsin, Milwaukee, Wisconsin
Johnny C. Hong
Affiliation:
Division of Transplant Surgery, Department of Surgery, Medical College of Wisconsin, Milwaukee, Wisconsin
Jennifer Arvan
Affiliation:
Department of Infection Prevention and Control, Froedtert Memorial Lutheran Hospital, Milwaukee, Wisconsin
Joshua W. Hyke
Affiliation:
Department of Infection Prevention and Control, Froedtert Memorial Lutheran Hospital, Milwaukee, Wisconsin
Louis Palen
Affiliation:
Department of Infection Prevention and Control, Froedtert Memorial Lutheran Hospital, Milwaukee, Wisconsin
Sabrina Savage
Affiliation:
Department of Infection Prevention and Control, Froedtert Memorial Lutheran Hospital, Milwaukee, Wisconsin
Heather Seliger
Affiliation:
Department of Infection Prevention and Control, Froedtert Memorial Lutheran Hospital, Milwaukee, Wisconsin
Susan Huerta
Affiliation:
Froedtert Memorial Lutheran Hospital, Milwaukee, Wisconsin
Nathan A. Ledeboer
Affiliation:
Department of Pathology, Medical College of Wisconsin, Milwaukee, Wisconsin
Shireen Kotay
Affiliation:
Division of Infectious Diseases, University of Virginia, Charlottesville, Virginia
Amy J. Mathers
Affiliation:
Division of Infectious Diseases, University of Virginia, Charlottesville, Virginia
Vaughn S. Cooper
Affiliation:
Department of Microbiology and Molecular Genetics, University of Pittsburgh, Pittsburgh, Pennsylvania
Mustapha Munir Mustapha
Affiliation:
Division of Infectious Diseases, University of Pittsburgh, Pittsburgh, Pennsylvania
Roberta T. Mettus
Affiliation:
Division of Infectious Diseases, University of Pittsburgh, Pittsburgh, Pennsylvania
Yohei Doi
Affiliation:
Division of Infectious Diseases, University of Pittsburgh, Pittsburgh, Pennsylvania
L. Silvia Munoz-Price*
Affiliation:
Division of Infectious Diseases, Department of Medicine, Medical College of Wisconsin, Milwaukee, Wisconsin
*
Author for correspondence: L. Silvia Munoz-Price, Email: [email protected]

Abstract

Objective:

Describe the epidemiological and molecular characteristics of an outbreak of Klebsiella pneumoniae carbapenemase (KPC)–producing organisms and the novel use of a cohorting unit for its control.

Design:

Observational study.

Setting:

A 566-room academic teaching facility in Milwaukee, Wisconsin.

Patients:

Solid-organ transplant recipients.

Methods:

Infection control bundles were used throughout the time of observation. All KPC cases were intermittently housed in a cohorting unit with dedicated nurses and nursing aids. The rooms used in the cohorting unit had anterooms where clean supplies and linens were placed. Spread of KPC-producing organisms was determined using rectal surveillance cultures on admission and weekly thereafter among all consecutive patients admitted to the involved units. KPC-positive strains underwent pulsed-field gel electrophoresis and whole-genome sequencing.

Results:

A total of 8 KPC cases (5 identified by surveillance) were identified from April 2016 to April 2017. After the index patient, 3 patients acquired KPC-producing organisms despite implementation of an infection control bundle. This prompted the use of a cohorting unit, which immediately halted transmission, and the single remaining KPC case was transferred out of the cohorting unit. However, additional KPC cases were identified within 2 months. Once the cohorting unit was reopened, no additional KPC cases occurred. The KPC-positive species identified during this outbreak included Klebsiella pneumoniae, Enterobacter cloacae complex, and Escherichia coli. blaKPC was identified on at least 2 plasmid backbones.

Conclusions:

A complex KPC outbreak involving both clonal and plasmid-mediated dissemination was controlled using weekly surveillances and a cohorting unit.

Type
Original Article
Copyright
© 2019 by The Society for Healthcare Epidemiology of America. All rights reserved 

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References

Antibiotic resistance. World Health Organization website. http://www.who.int/news-room/fact-sheets/detail/antibiotic-resistance. Published 2016. Accessed July 18, 2018.Google Scholar
Nordmann, P, Cuzon, G, Naas, T. The real threat of Klebsiella pneumoniae carbapenemase-producing bacteria. Lancet Infect Dis 2009;9:228236.CrossRefGoogle ScholarPubMed
Tracking CRE. Centers for Disease Control and Prevention website. https://www.cdc.gov/hai/organisms/cre/trackingcre.html. Published 2017. Accessed July 18, 2018.Google Scholar
Logan, LK, Weinstein, RA. The epidemiology of carbapenem-resistant Enterobacteriaceae: the impact and evolution of a global menace. J Infect Dis 2017;215:S28S36.CrossRefGoogle ScholarPubMed
CRE control and prevention toolkit. Agency for Healthcare Research and Quality website. https://www.ahrq.gov/professionals/quality-patient-safety/patient-safety-resources/resources/cretoolkit/index.html. Published 2014. Accessed July 18, 2018.Google Scholar
Multiplex real-time PCR detection of Klebsiella pneumoniae carbapenemase (KPC) and New Delhi metallo-β-lactamase (NDM-1) genes. Centers for Disease Control and Prevention website. https://www.cdc.gov/hai/pdfs/labsettings/KPC-NDM-protocol-2011.pdf. Published 2011. Accessed July 18, 2018.Google Scholar
Mathers, AJ, Vegesana, K, German Mesner, I, et al. Intensive care unit wastewater interventions to prevent transmission of multi-species Klebsiella pneumoniae carbapenemase (KPC) producing organisms. Clin Infect Dis 2018;67:171178.CrossRefGoogle Scholar
Kim, YA, Qureshi, ZA, Adams-Haduch, JM, Park, YS, Shutt, KA, Doi, Y. Features of infections due to Klebsiella pneumoniae carbapenemase-producing Escherichia coli: emergence of sequence type 131. Clin Infect Dis 2012;55:224231.CrossRefGoogle ScholarPubMed
Bueno, MFC, Francisco, GR, O’Hara, JA, De Oliveira Garcia, D, Doi, Y. Coproduction of 16S rRNA methyltransferase RmtD or RmtG with KPC-2 and CTX-M group extended-spectrum β-lactamases in Klebsiella pneumoniae. Antimicrob Agents Chemother 2013;57:23972400.CrossRefGoogle ScholarPubMed
Munoz-Price, LS, Hayden, MK, Lolans, K, et al. Successful control of an outbreak of Klebsiella pneumoniae carbapenemase-producing K. pneumoniae at a long-term acute care hospital. Infect Control Hosp Epidemiol 2010;4:341347.CrossRefGoogle Scholar
Munoz-Price, LS, De La Cuesta, C, Adams, S, et al. Successful eradication of a monoclonal strain of Klebsiella pneumoniae during a K. pneumoniae carbapenemase-producing K. pneumoniae outbreak in a surgical intensive care unit in Miami, Florida. Infect Control Hosp Epidemiol 2010;10:10741077.CrossRefGoogle Scholar
Gohil, SK, Singh, R, Chang, J, et al. Emergence of carbapenem-resistant Enterobacteriaceae in Orange County, California, and support for early regional strategies to limit spread. Am J Infect Control 2017;45:11771182.CrossRefGoogle ScholarPubMed
Khan, AS, Dancer, SJ, Humphreys, H. Priorities in the prevention and control of multidrug-resistant Enterobacteriaceae in hospitals J Hosp Infect 2012;82:8593.CrossRefGoogle ScholarPubMed
Palmore, TN, Henderson, DK. Managing transmission of carbapenem-resistant enterobacteriaceae in healthcare settings: a view from the trenches. Clin Infect Dis 2013;57:15931599.CrossRefGoogle ScholarPubMed
Munoz-Price, LS, Quinn, JP. Deconstructing the infection control bundles for the containment of carbapenem-resistant Enterobacteriaceae. Curr Opin Infect Dis 2013;26:378387.CrossRefGoogle ScholarPubMed
Kotay, S, Chai, W, Guilford, W, Barry, K, Mathers, AJ. Spread from the sink to the patient: In situ study using green fluorescent protein (GFP)-expressing Escherichia coli to model bacterial dispersion from hand-washing sink-trap reservoirs. Appl Environ Microbiol 2017;83:e0332716.CrossRefGoogle ScholarPubMed
Kizny Gordon, AE, Mathers, AJ, Cheong, EYL, et al. The hospital water environment as a reservoir for carbapenem-resistant organisms causing hospital-acquired infections—a systematic review of the literature. Clin Infect Dis 2017;64:14351444.CrossRefGoogle ScholarPubMed
Naas, T, Bonnin, RA, Cuzon, G, Villegas, MV, Nordmann, P. Complete sequence of two KPC-harbouring plasmids from Pseudomonas aeruginosa. J Antimicrob Chemother 2013;68:17571762.CrossRefGoogle ScholarPubMed
Yao, Y, Lazaro-Perona, F, Falgenhauer, L, et al. Insights into a novel blaKPC-2-Encoding IncP-6 plasmid reveal carbapenem-resistance circulation in several Enterobacteriaceae species from wastewater and a hospital source in Spain. Front Microbiol 2017;8:1143.CrossRefGoogle Scholar
Kukla, R, Chudejova, K, Papagiannitsis, CC, et al. Characterization of KPC-encoding plasmids from enterobacteriaceae isolated in a Czech hospital. Antimicrob Agents Chemother 2018;62:e0215217.Google Scholar
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