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Reduced Use of Third-Generation Cephalosporins Decreases the Acquisition of Extended-Spectrum Beta-Lactamase-Producing Klebsiella pneumoniae

Published online by Cambridge University Press:  02 January 2015

Sang-Oh Lee
Affiliation:
Division of Infectious Diseases, Gil Medical Center, Gachon Medical School, Incheon, Korea
Eun Sun Lee
Affiliation:
Infection Control Unit, Gil Medical Center, Gachon Medical School, Incheon, Korea
Shin Young Park
Affiliation:
Infection Control Unit, Gil Medical Center, Gachon Medical School, Incheon, Korea
Sue-Yun Kim
Affiliation:
Division of Infectious Diseases, Gil Medical Center, Gachon Medical School, Incheon, Korea
Yiel-Hae Seo
Affiliation:
Department of Laboratory Medicine, Gil Medical Center, Gachon Medical School, Incheon, Korea
Yong Kyun Cho*
Affiliation:
Division of Infectious Diseases, Gil Medical Center, Gachon Medical School, Incheon, Korea
*
Division of Infectious Diseases, Gil Medical Center, Gachon Medical School, 1198 Guwol-dong, Namdong-gu, Incheon 405-760, Korea

Abstract

Objectives:

To identify risk factors for the respiratory acquisition of extended-spectrum beta-lactamase (ESBL)-producing Klebsiella pneumoniae among patients admitted to a neurosurgical intensive care unit (NSICU) and to modify them without changing general infection control measures.

Design:

Nested case-control and intervention study.

Setting:

A 1,200-bed, tertiary-care teaching hospital with a 17-bed NSICU.

Methods:

Sputa of all patients admitted to the NSICU were cultured weekly during the study. From October 2002 through February 2003, 29 case-patients from whose sputum ESBL-producing K. pneumoniae was isolated were detected and 59 controls-patients were randomly selected among patients without any positive isolate of ESBL-producing K. pneumoniae. After analyzing the risk factors, we intervened to modify them and compared the acquisition rate of ESBL-producing K. pneumoniae before (October 2002 to February 2003) and after (April to August 2003) the intervention.

Results:

Multivariate analysis showed that prior exposure to third-generation cephalosporins (TGCs) (OR, 6.0; CI95, 1.9 to 18.6; P= .002) was an independent risk factor of ESBL-producing K. pneumoniae acquisition. The neurosurgical team was notified of the result, and the infectious diseases specialist visited the NSICU three times a week to regulate TGC use during the intervention period. Patients admitted before the intervention were older than patients admitted after. The respiratory acquisition of ESBL-producing K. pneumoniae per 1,000 patient-days (13.5 [CI95, 8.9 to 18.1] vs 2.7 [CI95, 0.9 to 4.6]) and the antimicrobial use density of TGCs (38.2 ± 5.0 vs 17.3 ± 2.6; P < .001) decreased significantly after the intervention.

Conclusion:

Prior exposure to TGCs was an independent risk factor for the respiratory acquisition of ESBL-producing K. pneumoniae, and less use of TGCs was associated with a decrease in acquisition.

Type
Orginal Articles
Copyright
Copyright © The Society for Healthcare Epidemiology of America 2004 

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References

1. Bush, K, Jacoby, GA, Medeiros, AA. A functional classification scheme for beta-lactamases and its correlation with molecular structure. Antimicrob Agents Chemother 1995;39:12111233.10.1128/AAC.39.6.1211Google Scholar
2. Nouvellon, M, Pons, JL, Sirot, D, Combe, ML, Lemeland, JF. Clonal outbreaks of extended-spectrum beta-lactamase-producing strains of Klebsiella pneumoniae demonstrated by antibiotic susceptibility testing, beta-lactamase typing, and multilocus enzyme electrophoresis. J Clin Microbiol 1994;32:26252627.10.1128/jcm.32.10.2625-2627.1994Google Scholar
3. Rice, LB, Willey, SH, Papanicolaou, GB, et al. Outbreak of ceftazidime resistance caused by extended-spectrum beta-lactamases at a Massachusetts chronic-care facility. Antimicrob Agents Chemother 1990;34:21932199.10.1128/AAC.34.11.2193Google Scholar
4. Ayan, M, Kuzucu, C, Durmaz, R, Aktas, E, Cizmeci, Z. Analysis of three outbreaks due to Klebsiella species in a neonatal intensive care unit. Infect Control Hosp Epidemiol 2003;24:495500.10.1086/502245Google Scholar
5. Meyer, KS, Urban, C, Eagan, JA, Berger, BJ, Rahal, JJ. Nosocomial outbreak of Klebsiella infection resistant to late-generation cephalosporins. Ann Intern Med 1993;119:353358.10.7326/0003-4819-119-5-199309010-00001Google Scholar
6. Peña, C, Pujol, M, Ardanuy, C, et al. Epidemiology and successful control of a large outbreak due to Klebsiella pneumoniae producing extended-spectrum beta-lactamases. Antimicrob Agents Chemother 1998;42:5358.10.1128/AAC.42.1.53Google Scholar
7. Patterson, JE, Hardin, TC, Kelly, CA, Garcia, RC, Jorgensen, JH. Association of antibiotic utilization measures and control of multiple-drug resistance in Klebsiella pneumoniae . Infect Control Hosp Epidemiol 2000;21:455458.Google Scholar
8. Rice, LB, Eckstein, EC, DeVente, J, Shlaes, DM. Ceftazidime-resistant Klebsiella pneumoniae isolates recovered at the Cleveland Department of Veterans Affairs Medical Center. Clin Infect Dis 1996;23:118124.10.1093/clinids/23.1.118Google Scholar
9. Rahal, JJ, Urban, C, Horn, D, et al. Class restriction of cephalosporin use to control total cephalosporin resistance in nosocomial Klebsiella . JAMA 1998;280:12331237.Google Scholar
10. Asensio, A, Oliver, A, González-Diego, P, et al. Outbreak of a multiresis-tant Klebsiella pneumoniae strain in an intensive care unit: antibiotic use as risk factor for colonization and infection. Clin Infect Dis 2000;30:5560.10.1086/313590Google Scholar
11. Lin, MF, Huang, ML, Lai, SH. Risk factors in the acquisition of extended-spectrum beta-lactamase Klebsiella pneumoniae: a case-control study in a district teaching hospital in Taiwan. J Hosp Infect 2003;53:3945.10.1053/jhin.2002.1331Google Scholar
12. Pessoa-Silva, CL, Moreira, BM, Almeida, VC, et al. Extended-spectrum beta-lactamase-producing Klebsiella pneumoniae in a neonatal intensive care unit: risk factors for infection and colonization. J Hosp Infect 2003;53:198206.10.1053/jhin.2002.1373Google Scholar
13. Jarlier, V, Nicolas, MH, Fournier, G, Philippon, A. Extended broad-spectrum beta-lactamases conferring transferable resistance to newer beta-lactam agents in Enterobacteriaceae: hospital prevalence and susceptibility patterns. Rev Infect Dis 1988;10:867878.10.1093/clinids/10.4.867Google Scholar
14. National Committee for Clinical Laboratory Standards. Performance Standards for Antimicrobial Susceptibility Testing. Wayne, PA: National Committee for Clinical Laboratory Standards; 2003. Approved standard M7-A6.Google Scholar
15. Fridkin, SK, Steward, CD, Edwards, JR, et al. Surveillance of antimicrobial use and antimicrobial resistance in United States hospitals: project ICARE phase 2. Clin Infect Dis 1999;29:245252.Google Scholar
16. Garner, JS, Jarvis, WR, Emori, TG, Horan, TC, Hughes, JM. CDC definitions for nosocomial infections, 1988. Am J Infect Control 1988;16:128140.10.1016/0196-6553(88)90053-3Google Scholar
17. Rice, LB. Controlling antibiotic resistance in the ICU: different bacteria, different strategies. Cleve Clin J Med 2003;70:793800.10.3949/ccjm.70.9.793Google Scholar