Hostname: page-component-cd9895bd7-gxg78 Total loading time: 0 Render date: 2024-12-22T22:07:48.108Z Has data issue: false hasContentIssue false

Successful Control of an Outbreak of Klebsiella pneumoniae Carbapenemase—Producing K. pneumoniae at a Long-Term Acute Care Hospital

Published online by Cambridge University Press:  02 January 2015

L. Silvia Munoz-Price*
Affiliation:
Division of Infectious Diseases, University of Miami, Florida Jackson Memorial Hospital, Miami, Florida Munster, Alverno Laboratories, Hammond, Indiana
Mary K. Hayden
Affiliation:
Rush University, Chicago, Illinos
Karen Lolans
Affiliation:
Rush University, Chicago, Illinos
Sarah Won
Affiliation:
Rush University, Chicago, Illinos Stroger (Cook County) Hospital, Chicago, Illinos
Michael Lin
Affiliation:
Rush University, Chicago, Illinos
Alexander Sterner
Affiliation:
Munster, Alverno Laboratories, Hammond, Indiana
Robert A. Weinstein
Affiliation:
Rush University, Chicago, Illinos Stroger (Cook County) Hospital, Chicago, Illinos
*
Jackson Memorial Hospital, Park Plaza West L-302, 1611 Northwest 12th Avenue, Miami, PL 33136-1096 ([email protected])

Abstract

Objective.

To determine the effect of a bundle of infection control interventions on the horizontal transmission of Klebsiella pneumoniae carbapenemase (KPC)-producing K. pneumoniae during an outbreak.

Design.

Quasi-experimental study.

Setting.

Long-term acute care hospital.

Intervention.

On July 23,2008, a bundled intervention was implemented: daily 2% Chlorhexidine gluconate baths for patients, enhanced environmental cleaning, surveillance cultures at admission, serial point prevalence surveillance (PPS), isolation precautions, and training of personnel. Baseline PPS was performed before the intervention was implemented. Any gram-negative rod isolate suspected of KPC production underwent a modified Hodge test and, if results were positive, confirmatory polymerase chain reaction testing. Clinical cases were defined to occur for patients whose samples yielded KPC-positive gram-negative rods in clinical cultures.

Results.

Baseline PPS performed on June 17, 2008, showed a prevalence of colonization with KPC-producing isolates of 21% (8 of 39 patients screened). After implementation of the intervention, monthly PPS was performed 5 times, which showed prevalences of colonization with KPC-producing isolates of 12%, 5%, 3%, 0%, and 0% (P < .001). From January 1, 2008, until the intervention, 8 KPC-positive clinical cases—suspected to be due to horizontal transmission—were detected. From implementation of the intervention through December 31, 2008, only 2 KPC-positive clinical cases, both in August 2008, were detected. From January 1 through December 31, 2008, 8 patients were detected as carriers of KPC-producing isolates at admission to the institution, 4 patients before and 4 patients after the intervention.

Conclusion.

A bundled intervention was successful in preventing horizontal spread of KPC-producing gram-negative rods in a long-term acute care hospital, despite ongoing admission of patients colonized with KPC producers.

Type
Original Articles
Copyright
Copyright © The Society for Healthcare Epidemiology of America 2010

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

1. Yigit, H, Queenan, AM, Anderson, GJ, et al. Novel carbapenem-hydro-lyzing β-lactamase, KPC-1, from a carbapenem-resistant strain of Klebsiella pneumoniae . Antimicrob Agents Chemother 2001;45:11511161.CrossRefGoogle ScholarPubMed
2. Villegas, MV, Lolans, K, Correa, A, Kattan, JN, Lopez, JA, Quinn, JP. First identification of Pseudomonas aeruginosa isolates producing a KPC-type carbapenem-hydrolyzing β-lactamase. Antimicrob Agents Chemother 2007;51:15531555.Google Scholar
3. Bratu, S, Brooks, S, Burney, S, et al. Detection and spread of Escherichia coli possessing the plasmid-borne carbapenemase KPC-2 in Brooklyn, New York. Clin Infect Dis 2007;44:972975.Google Scholar
4. Bratu, S, Landman, D, Alam, M, Tolentino, E, Quale, J. Detection of KPC carbapenem-hydrolyzing enzymes in Enterobacter spp. from Brooklyn, New York. Antimicrob Agents Chemother 2005;49:776778.Google Scholar
5. Miriagou, V, Tzouvelekis, LS, Rossiter, S, Tzelepi, E, Angulo, FJ, Whichard, JM. Imipenem resistance in a Salmonella clinical strain due to plasmid-mediated class A carbapenemase KPC-2. Antimicrob Agents Chemother 2003;47:12971300.CrossRefGoogle Scholar
6. Cai, JC, Zhou, HW, Zhang, R, Chen, GX. Emergence of Serratia marcescens, Klebsiella pneumoniae, and Escherichia coli isolates possessing the plas-mid-mediated carbapenem-hydrolyzing β-lactamase KPC-2 in intensive care units of a Chinese hospital. Antimicrob Agents Chemother 2008;52: 20142018.Google Scholar
7. Bratu, S, Mooty, M, Nichani, S, et al. Emergence of KPC-possessing Klebsiella pneumoniae in Brooklyn, New York: epidemiology and recommendations for detection. Antimicrob Agents Chemother 2005;49:30183020.CrossRefGoogle ScholarPubMed
8. Chmelnitsky, I, Navon-Venezia, S, Strahilevitz, J, Carmeli, Y. Plasmid-me-diated qnrB2 and carbapenemase gene bla(KPC-2) carried on the same plasmid in carbapenem-resistant ciprofloxacin-susceptible Enterobacter cloacae isolates. Antimicrob Agents Chemother 2008;52:29622965.CrossRefGoogle ScholarPubMed
9. Bratu, S, Tolaney, P, Karumudi, U, et al. Carbapenemase-producing Klebsiella pneumoniae in Brooklyn, NY: molecular epidemiology and in vitro activity of polymyxin B and other agents. J Antimicrob Chemother 2005;56:128132.Google Scholar
10. Moland, ES, Hanson, ND, Herrera, VL, et al. Plasmid-mediated, carba-penem-hydrolysing β-lactamase, KPC-2, in Klebsiella pneumoniae isolates. J Antimicrob Chemother 2003;51:711714.CrossRefGoogle Scholar
11. Bradford, PA, Bratu, S, Urban, C, et al. Emergence of carbapenem-resistant Klebsiella species possessing the class A carbapenem-hydrolyzing KPC-2 and inhibitor-resistant TEM-30 β-lactamases in New York City. Clin Infect Dis 2004;39:5560.Google Scholar
12. Bratu, S, Landman, D, Haag, R, et al. Rapid spread of carbapenem-resistant Klebsiella pneumoniae in New York City: a new threat to our antibiotic armamentarium. Arch Intern Med 2005;165:14301435.Google Scholar
13. Deshpande, LM, Rhomberg, PR, Sader, HS, Jones, RN. Emergence of serine carbapenemases (KPC and SME) among clinical strains of Enterobac-teriaceae isolated in the United States Medical Centers: report from the MYSTIC Program (1999-2005). Diagn Microbiol Infect Dis 2006;56:367372.CrossRefGoogle Scholar
14. Urban, C, Bradford, PA, Tuckman, M, et al. Carbapenem-resistant Escherichia coli harboring Klebsiella pneumoniae carbapenemase β-lactamases associated with long-term care facilities. Clin Infect Dis 2008;46:e127e130.Google Scholar
15. Villegas, MV, Lolans, K, Correa, A, et al. First detection of the plasmid-mediated class A carbapenemase KPC-2 in clinical isolates of Klebsiella pneumoniae from South America. Antimicrob Agents Chemother 2006;50: 28802882.CrossRefGoogle Scholar
16. Cuzon, G, Naas, T, Demachy, MC, Nordmann, P. Plasmid-mediated carbapenem-hydrolyzing β-lactamase KPC-2 in Klebsiella pneumoniae isolate from Greece. Antimicrob Agents Chemother 2008;52:796797.CrossRefGoogle ScholarPubMed
17. Monteiro, J, Santos, AF, Asensi, MD, Peirano, G, Gales, AC. First report of KPC-2-producing Klebsiella pneumoniae strains in Brazil. Antimicrob Agents Chemother 2009;53:333334.Google Scholar
18. Naas, T, Nordmann, P, Vedel, G, Poyart, C. Plasmid-mediated carbapenem-hydrolyzing β-lactamase KPC in a Klebsiella pneumoniae isolate from France. Antimicrob Agents Chemother 2005;49:44234424.CrossRefGoogle Scholar
19. Won, S, Munoz-Price, LS, Lolans, K, et al. Multi-facility emergence and rapid spread of KPC+ Enterobacteriaceae in northwest Indiana (NWI) and Illinois (IL). In: Programs and Abstracts of the 19th Annual Scientific Meeting of the Society for Healthcare Epidemiology of America (San Diego). Arlington, VA: Society for Healthcare Epidemiology of America; 2009; Abstract 67.Google Scholar
20. Munoz-Price, LS. Long-term acute care hospitals. Clin Infect Dis 2009;49: 438443.CrossRefGoogle ScholarPubMed
21. Gould, CV, Rothenberg, R, Steinberg, JP. Antibiotic resistance in long-term acute care hospitals: the perfect storm. Infect Control Hosp Epidemiol 2006;27:920925.Google Scholar
22. Anderson, KF, Lonsway, DR, Rasheed, JK, et al. Evaluation of methods to identify the Klebsiella pneumoniae carbapenemase in Enterobacteriaceae. J Clin Microbiol 2007;45:27232725.Google Scholar
23. Matushek, MG, Bonten, MJ, Hayden, MK. Rapid preparation of bacterial DNA for pulsed-field gel electrophoresis. J Clin Microbiol 1996;34:25982600.Google Scholar
24. Tenover, FC, Arbeit, RD, Goering, R, et al. Interpreting chromosomal DNA restriction patterns produced by pulsed-fieid gel electrophoresis: criteria for bacterial strain typing. J Clin Microbiol 1995;33:22332239.Google Scholar
25. Munoz-Price, LS, Hota, B, Stermer, A, Weinstein, RA. Prevention of bloodstream infections using daily Chlorhexidine baths at a long-term acute care hospital. Infect Control Hosp Epidemiol 2009;30:10311035.Google Scholar
26. Siegel, JD, Rhinehart, E, Jackson, M, Chiarello, L. 2007 Guideline for isolation precautions: preventing transmission of infectious agents in health care settings. Am J Infect Control 2007;35(10 Suppl 2):S65S164.CrossRefGoogle ScholarPubMed
27. Guidance for control of infections with carbapenem-resistant or carbape-nemase-producing Enterobacteriaceae in acute care facilities. MMWR Morb Mortal Wkly Rep 2009;58:256260.Google Scholar
28. Vernon, MO, Hayden, MK, Trick, WE, Hayes, RA, Blom, DW, Weinstein, RA. Chlorhexidine gluconate to cleanse patients in a medical intensive care unit: the effectiveness of source control to reduce the bioburden of vancomycin-resistant enterococci. Arch Intern Med 2006;166:306312.Google Scholar
29. Larson, EL, Cimiotti, JP, Haas, J, et al. Gram-negative bacilli associated with catheter-associated and non-catheter-associated bloodstream infections and hand carriage by healthcare workers in neonatal intensive care units. Pediatr Crit Care Med 2005;6:457461.CrossRefGoogle ScholarPubMed