Hostname: page-component-586b7cd67f-rcrh6 Total loading time: 0 Render date: 2024-11-29T00:43:53.108Z Has data issue: false hasContentIssue false

A National Intervention to Prevent the Spread of Carbapenem-Resistant Enterobacteriaceae in Israeli Post-Acute Care Hospitals

Published online by Cambridge University Press:  10 May 2016

Debby Ben-David*
Affiliation:
National Center for Infection Control, Israel Ministry of Health, Tel Aviv, Israel
Samira Masarwa
Affiliation:
National Center for Infection Control, Israel Ministry of Health, Tel Aviv, Israel
Amos Adler
Affiliation:
National Center for Infection Control, Israel Ministry of Health, Tel Aviv, Israel
Hagit Mishali
Affiliation:
National Center for Infection Control, Israel Ministry of Health, Tel Aviv, Israel
Yehuda Carmeli
Affiliation:
National Center for Infection Control, Israel Ministry of Health, Tel Aviv, Israel
Mitchell J. Schwaber
Affiliation:
National Center for Infection Control, Israel Ministry of Health, Tel Aviv, Israel
*
National Center for Infection Control, Israel Ministry of Health, 6 Weizmann Street, Tel Aviv 64239, Israel ([email protected]).

Extract

Objective

Patients hospitalized in post-acute care hospitals (PACHs) constitute an important reservoir of antimicrobial-resistant bacteria. High carriage prevalence of carbapenem-resistant Enterobacteriaceae (CRE) has been observed among patients hospitalized in PACHs. The objective of the study is to describe the impact of a national infection control intervention on the prevalence of CRE in PACHs.

Design

A prospective cohort interventional study.

Setting

Thirteen PACHs in Israel.

Intervention

A multifaceted intervention was initiated between 2008 and 2011 as part of a national program involving all Israeli healthcare facilities. The intervention has included (1) periodic on-site assessments of infection control policies and resources, using a score comprised of 16 elements; (2) assessment of risk factors for CRE colonization; (3) development of national guidelines for CRE control in PACHs involving active surveillance and contact isolation of carriers; and (4) 3 cross-sectional surveys of rectal carriage of CRE that were conducted in representative wards.

Results

The infection control score increased from 6.8 to 14.0 (P < .001) over the course of the study period. A total of 3,516 patients were screened in the 3 surveys. Prevalence of carriage among those not known to be carriers decreased from 12.1% to 7.9% (P = .008). Overall carrier prevalence decreased from 16.8% to 12.5% (P = .013). Availability of alcohol-based hand rub, appropriate use of gloves, and a policy of CRE surveillance at admission to the hospital were independently associated with lower new carrier prevalence.

Conclusion

A nationwide infection control intervention was associated with enhanced infection control measures and a reduction in the prevalence of CRE in PACHs.

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

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.)

Footnotes

a

Members of the Post-Acute Care Hospital Carbapenem-Resistant Enterobacteriaceae Working Group are listed at the end of the text.

References

1. Gould, CV, Rothenberg, R, Steinberg, JP. Antibiotic resistance in long-term acute care hospitals: the perfect storm. Infect Control Hosp Epidemiol 2006;27(9):920925.Google Scholar
2. Munoz-Price, LS. Long-term acute care hospitals. Clin Infect Dis 2009;49(3):438443.Google Scholar
3. Furuno, JP, Hebden, JN, Standiford, HC, et al. Prevalence of methicillin-resistant Staphylococcus aureus and Acinetobacter baumannii in a long-term acute care facility. Am J Infect Control 2008;36(7):468471.Google Scholar
4. Stephens, C, Francis, SJ, Abell, V, DiPersio, JR, Wells, P. Emergence of resistant Acinetobacter baumannii in critically ill patients within an acute care teaching hospital and a long-term acute care hospital. Am J Infect Control 2007;35(4):212215.Google Scholar
5. Barnes, SL, Harris, AD, Golden, BL, Wasil, EA, Furuno, JP. Contribution of interfacility patient movement to overall methicillin-resistant Staphylococcus aureus prevalence levels. Infect Control Hosp Epidemiol 2011;32(11):10731078.Google Scholar
6. Munoz-Price, LS, Stemer, A. Four years of surveillance cultures at a long-term acute care hospital. Infect Control Hosp Epidemiol 2010;31(1):5963.CrossRefGoogle Scholar
7. Kahn, JM, Benson, NM, Appleby, D, Carson, SS, Iwashyna, TJ. Long-term acute care hospital utilization after critical illness. JAMA 2010;303(22):22532259.Google Scholar
8. Nicolle, LE. Infection control in long-term care facilities. Clin Infect Dis 2000;31(3):752756.CrossRefGoogle ScholarPubMed
9. Roup, BJ, Roche, JC, Pass, M. Infection control program disparities between acute and long-term care facilities in Maryland. Am J Infect Control 2006;34(3):122127.Google Scholar
10. Jones, M, Samore, MH, Carter, M, Rubin, MA. Long-term care facilities in Utah: a description of human and information technology resources applied to infection control practice. Am J Infect Control 2012;40(5):446450.Google Scholar
11. Schwaber, MJ, Carmeli, Y. Carbapenem-resistant Enterobacteriaceae: a potential threat. JAMA 2008;300(24):29112913.Google Scholar
12. Nordmann, P, Naas, T, Poirel, L. Global spread of carbapenemase-producing Enterobacteriaceae. Emerg Infect Dis 2011;17(10):17911798.Google Scholar
13. Cuzon, G, Naas, T, Truong, H, et al. Worldwide diversity of Klebsiella pneumoniae that produce beta-lactamase blaKPC-2 gene. Emerg Infect Dis 2010;16(9):13491356.Google Scholar
14. Nordmann, P, Cuzon, G, Naas, T. The real threat of Klebsiella pneumoniae carbapenemase-producing bacteria. Lancet Infect Dis 2009;9(4):228236.Google Scholar
15. Navon-Venezia, S, Leavitt, A, Schwaber, MJ, et al. First report on a hyperepidemic clone of KPC-3-producing Klebsiella pneumoniae in Israel genetically related to a strain causing outbreaks in the United States. Antimicrob. Agents Chemother 2009;53(2):818820.CrossRefGoogle ScholarPubMed
16. Sisto, A, D’Ancona, F, Meledandri, M, et al. Carbapenem non-susceptible Klebsiella pneumoniae from Micronet network hospitals, Italy, 2009 to 2012. Euro Surveill 2012;17(33). pii: 20247.CrossRefGoogle ScholarPubMed
17. Samra, Z, Ofir, O, Lishtzinsky, Y, Madar-Shapiro, L, Bishara, J. Outbreak of carbapenem-resistant Klebsiella pneumoniae producing KPC-3 in a tertiary medical centre in Israel. Int J Antimicrob Agents 2007;30(6):525529.Google Scholar
18. Souli, M, Galani, I, Giamarellou, H. Emergence of extensively drug-resistant and pandrug-resistant gram-negative bacilli in Europe. Euro Surveill 2008;13(47). pii: 19045.Google Scholar
19. Schwaber, MJ, Lev, B, Israeli, A, et al. Containment of a country-wide outbreak of carbapenem-resistant Klebsiella pneumoniae in Israeli hospitals via a nationally implemented intervention. Clin Infect Dis 2011;52(7):848855.Google Scholar
20. Ben-David, D, Masarwa, S, Navon-Venezia, S, et al. Carbapenem-resistant Klebsiella pneumoniae in post-acute-care facilities in Israel. Infect Control Hosp Epidemiol 2011;32(9):845853.Google Scholar
21. Clinical and Laboratory Standards Institute. Performance standards for antimicrobial susceptibility testing; 20th informational supplement. Approved standard MS100-S20. Wayne, PA: Clinical and Laboratory Standards Institute, 2010.Google Scholar
22. Pittet, D, Allegranzi, B, Boyce, J; World Health Organization World Alliance for Patient Safety First Global Patient Safety Challenge Core Group of Experts. The World Health Organization guidelines on hand hygiene in health care and their consensus recommendations. Infect Control Hosp Epidemiol 2009;30(7):611622.CrossRefGoogle Scholar
23. Siegel, JD, Rhinehart, E, Jackson, M, Chiarello, L; Health Care Infection Control Practices Advisory Committee. 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
24. Ostrowsky, BE, Trick, WE, Sohn, AH, et al. Control of vancomycin-resistant enterococcus in health care facilities in a region. N Engl J Med 2001;344(19):14271433.CrossRefGoogle ScholarPubMed
25. Chitnis, AS, Caruthers, PS, Rao, AK, et al. Outbreak of carbapenem-resistant Enterobacteriaceae at a long-term acute care hospital: sustained reductions in transmission through active surveillance and targeted interventions. Infect Control Hosp Epidemiol 2012;33(10):984992.CrossRefGoogle Scholar
26. Oteo, J, Navarro, C, Cercenado, E, et al. Spread of Escherichia coli strains with high-level cefotaxime and ceftazidime resistance between the community, long-term care facilities, and hospital institutions. J Clin Microbiol 2006;44(7):23592366.Google Scholar
27. Viau, RA, Hujer, AM, Marshall, SH, et al. “Silent” dissemination of Klebsiella pneumoniae isolates bearing K. pneumoniae carbapenemase in a long-term care facility for children and young adults in northeast Ohio. Clin Infect Dis 2012;54(9):13141321.Google Scholar
28. Won, SY, Munoz-Price, LS, Lolans, K, Hota, B, Weinstein, RA, Hayden, MK. Emergence and rapid regional spread of Klebsiella pneumoniae carbapenemasea producing Enterobacteriaceae. Clin Infect Dis 2011;53(6):532540.Google Scholar
29. Carbapenem-resistant Klebsiella pneumoniae associated with a long-term care facility, West Virginia, 2009–2011. MMWR Morb Mortal Wkly Rep 2011;60(41):14181420.Google Scholar
30. Marchaim, D, Chopra, T, Bogan, C, et al. The burden of multidrug-resistant organisms on tertiary hospitals posed by patients with recent stays in long-term acute care facilities. Am J Infect Control 2012;40(8):760765.Google Scholar
31. Prabaker, K, Lin, MY, McNally, M, et al. Transfer from high-acuity long-term care facilities is associated with carriage of Klebsiella pneumoniae carbapenemase-producing Enterobacteriacea: a multihospital study. Infect Control Hosp Epidemiol 2012;33(12):11931199.Google Scholar
32. Schwaber, MJ, Carmeli, Y. An ongoing national intervention to contain the spread of carbapenem-resistant Enterobacteriaceae. Clin Infect Dis 2014;58(5):697703 Google Scholar
33. Jarlier, V, Trystram, D, Brun-Buisson, C, et al. Curbing methicillin-resistant Staphylococcus aureus in 38 French hospitals through a 15-year institutional control program. Arch Intern Med 2010;170(6):552559.Google Scholar
34. Nicolle, LE. Antimicrobial resistance in long-term care facilities. Future Microbiol 2012;7(2):171174.Google Scholar
35. Calfee, D, Jenkins, SG. Use of active surveillance cultures to detect asymptomatic colonization with carbapenem-resistant Klebsiella pneumoniae in intensive care unit patients. Infect Control Hosp Epidemiol 2008;29(10):966968.Google Scholar
36. Ben-David, D, Maor, Y, Keller, N, et al. Potential role of active surveillance in the control of a hospital-wide outbreak of carbapenem-resistant Klebsiella pneumoniae infection. Infect Control Hosp Epidemiol 2010;31(6):620626.Google Scholar
37. Ciobotaro, P, Oved, M, Nadir, E, Bardenstein, R, Zimhony, O. An effective intervention to limit the spread of an epidemic carbapenem-resistant Klebsiella pneumoniae strain in an acute care setting: from theory to practice. Am J Infect Control 2011;39(8):671677.Google Scholar
38. Kochar, S, Sheard, T, Sharma, R, et al. Success of an infection control program to reduce the spread of carbapenem-resistant Klebsiella pneumoniae . Infect Control Hosp Epidemiol 2009;30(5):447452.Google Scholar
39. Thurlow, CJ, Prabaker, K, Lin, MY, Lolans, K, Weinstein, RA, Hayden, MK. Anatomic sites of patient colonization and environmental contamination with Klebsiella pneumoniae carbapenemase-producing Enterobacteriaceae at long-term acute care hospitals. Infect Control Hosp Epidemiol 2013;34(1):5661.Google Scholar