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A Sustained Outbreak ofClostridium difficile in a General Hospital: Persistance of a Toxigenic Clone in Four Units

Published online by Cambridge University Press:  02 January 2015

Swapan K. Nath*
Affiliation:
Department of Laboratory Medicine, Henderson General Hospital Hamilton, Ontario, Canada
James H. Thornley
Affiliation:
Department of Laboratory Medicine, Henderson General Hospital Hamilton, Ontario, Canada
Mary Kelly
Affiliation:
Department of Laboratory Medicine, Henderson General Hospital Hamilton, Ontario, Canada
Bernadette Kucera
Affiliation:
Department of Infection Control, Henderson General Hospital Hamilton, Ontario, Canada
Stephen L.W. On
Affiliation:
National Collection of Type Cultures, Central Public Health Laboratory, London, England
Barry Holmes
Affiliation:
National Collection of Type Cultures, Central Public Health Laboratory, London, England
Menelaos Costas
Affiliation:
National Collection of Type Cultures, Central Public Health Laboratory, London, England
*
Department of Laboratory Medicine, Henderson General Hospital, Hamilton, Ontario, Canada, L8V 1C3

Abstract

Objective:

To evaluate the endemicity and epidemiology of toxigenic Clostridium difficile in a sustained outbreak of antibiotic-associated diarrhea.

Setting:

University-affiliated, 465-bed tertiary care teaching hospital with adjacent cancer clinic in Hamilton, Ontario.

Design:

From August 8, 1991, through August 31, 1993, a total of 187 cases were investigated for epidemiologic analysis of toxigenic C difficile from stool cultures, to identify the endemic clone(s). To assess the nature of contamination, cultures of inanimate surfaces in the patient environment from the four most affected units (medical teaching, nonteaching medical, hematologic oncology, and the intensive care unit) were processed for C difficile. The 229 clinical strains and 24 environmental strains isolated were typed by numerical analysis of SDS-PAGE protein patterns.

Results:

A majority (81%) of cases in the epidemiologic analysis were associated with a toxigenic electrophoretic (EP) type 1 C difficile that was identical to the strain first isolated from an index case that occurred 18 months before the start of this study. Culture and typing of the C difficile strains from the inanimate surfaces in the four most affected units showed that the patient environment was contaminated with the toxigenic EP type 1 organism. Six other strains that occurred infrequently among cases also were found in the environment.

Conclusions:

A single predominant toxigenic clone has been implicated in a sustained outbreak of antibiotic-associated diarrhea that affected elderly patients. The “endemic” clone transmitted for the 25-month study period was linked to an index case shedding a toxigenic EP type 1 strain that occurred 21 months prior to the initial outbreak on the medical teaching unit. The patient environment in the affected units was found to be contaminated with the same clone, possibly due to shedding of organisms by fecally incontinent symptomatic patients. The extrinsic factors contributing to the endemic transmission of this one clone still are not well understood

Type
Original Articles
Copyright
Copyright © The Society for Healthcare Epidemiology of America 1994

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References

1. Tedesco, FJ. Pseudomembranous colitis: pathogenesis and therapy. Med Clin North Am 1982;66:655664.Google Scholar
2. Peterson, LR, Kelly, PJ. The role of clinical microbiology laboratory in the management of Clostridium difficile-associated diarrhea. Infect Dis Clin North Am 1993;7:277294.Google Scholar
3. Brown, E, Talbot, GH, Axelrod, P, Provencher, M, Hoegg, C. Risk factors for Clostridium difficile toxin-associated diarrhea. Infect Control Hosb Ebidemiol 1990;11:283290.CrossRefGoogle ScholarPubMed
4. Thibault, A, Miller, MA, Gaese, C. Risk factors for the developement of Clostridium difficile-associated diarrhea during a hospital outbreak. Infect Control Hosp Ebidemiol 1991;12:345348.CrossRefGoogle Scholar
5. Pierce, PF, Wilson, R, Silva, J, et al: Antibiotic-associated pseudomembranous colitis: an epidemiologic investigation of a cluster of cases. J Infect Dis 1982;145:269274.Google Scholar
6. Wust, J, Sullivan, NM, Hardegger, V, Wilkins, TD. Investigation of an outbreak of antibiotic-associated colitis by various typing methods. J Clin Microbial 1982;16:10961101.Google Scholar
7. Nolan, NPM, Kelly, CP, Humphreys, JFH, et al. An epidemic of pseudomembranous colitis: importance of person-to-person spread. Gut 1987;28:14671473.Google Scholar
8. Heard, SR, Wren, B, Bamett, MJ, Thomas, JM, Tabaqchah, S. Clostridium dificile infection in patients with hematological malignant disease: risk factors, fecal toxins and pathogenic strains. EPidemiol Infect 1988;100:6372.CrossRefGoogle Scholar
9. Heard, Sk, O'Farrell, S, Holland, D, Crook, S, Bamett, MJ, Tabaqchali, S. The epidemiology of Clostridium dificile with use of a typing scheme: nosocomial acquisition and cross-infection among immunocompromised patients. J Infect Dis 1986;153:159162.CrossRefGoogle Scholar
10. Savage, AM, Alford, RH. Nosocomial spread of C dificile . Infect Control 1983;4:3133.Google Scholar
11. Malamou-Ladas, H, O'Farrell, S, Nash, JQ, Tabaqchali, S. Isolation of Clostridium difficile from patients and the environment of hospital wards. J Clin Pathol 1983;36:8892.Google Scholar
12. Mulligan, ME, George, WL, Rolfe, RD, Finegold, SM. Epidemiological aspects of Clostridium difficile-induced diarrhea and colitis. Am J Clin Nutr 1980;33:(suppl 11):25332538.CrossRefGoogle ScholarPubMed
13. Mulligan, ME, Rolfe, RD, Finegold, SM, George, WL. Contamination of a hospital environment by Clostridium dificile . Current Microbiology 1979;3:173175.CrossRefGoogle Scholar
14. Kim, K-H, Fekety, R, Batts, DH, et al. Isolation of Clostridium difficile from the environment and contacts of patients with antibiotic-associated colitis. J Infect Dis 1981;143:4250.CrossRefGoogle ScholarPubMed
15. Fekety, R, Kim, K-H, Brown, D, et al. Epidemiology of antibiotic-associated colitis: isolation ofClostridium difficile from the hospital environment. Am J Med 1981;70:906908.CrossRefGoogle Scholar
16. McFarland, LV, Mulligan, ME, Kwok, Rw, Stamm, WE. Nosocomial acquisition of Clostridium dificile infection. N Engl J Med 1989;320:204210.CrossRefGoogle Scholar
17. Costas, M, Holmes, B, On, SLW, Ganner, M, Kelly, MC, Nath, SK. Investigation of an outbreak of Clostridium dificile infection in a general hospital by numerical analysis of SDS-PAGE protein patterns. J Clin Microbial 1994;32:759765.CrossRefGoogle Scholar
18. Albert, R, Condi, F. Handwashing patterns in medical intensive-care units. N Engl J Med 1981:304:14651466.Google Scholar
19. George, WL, Sutter, VL, Citron, D, Finegold, S. Selective and differential medium for isolation of Clostridium dificile . J Clin Microbial 1979;9:214219.CrossRefGoogle Scholar
20. Holdeman, LV, Cato, EP, Moore, WEC. Anaerobe Laboratory Manual 4th ed. Blacksburg, VA Virginia Polytechnic Institute and State University; 1977.Google Scholar
21. Donta, ST, Shafter, SJ. Effects of Clostridium difficile toxin on tissue-cultured cells. J Infect Dis 1980;141:218227.CrossRefGoogle ScholarPubMed
22. Donta, ST, Sullivan, N, Willkins, TD. Differential effects of Clostridium dificile toxins on tissue-cultured cells. J Clin Microbiol 1982;15:11571158.CrossRefGoogle Scholar
23. Kaatz, GW, Gitlin, SD, Schaberg, DR, et al. Acquisition of Clostridium difficile from the hospital environment. Am J Epidemiol 1988;127:129194.Google Scholar
24. Delmée, M, Avesani, V. Virulence of ten serogroups of Clostridium dificile in hamsters. J Med Microbial 1990;33:8590.Google Scholar
25. Meisel-Mikolajczyk, F, Sokol, B. New Clostridium difficile serotypes in Poland. Eur J Epidemiol 1991;7:434436.Google Scholar
26. Toma, S, Lesiak, G, Magus, M, Lo, H-L, Delmée, M. Serotyping of Clostridium dificile. J Clin Microbial 1988;26:426428.CrossRefGoogle Scholar
27. Clabots, CR, Johnson, S, Bettin, KM, et al. Development of a rapid and efficient restriction endonuclease analysis typing system for Clostridium dificile with other typing systems. J Clin Microbial 1993;31:18701875.CrossRefGoogle Scholar
28. Delmée, M, Laroche, Y, Avesani, V, Cornelis, G. Comparison of serogrouping and polyacrylamide gel electrophoresis-for typing Clostridium difficile . I Clin Microbial 1986:24:991994.CrossRefGoogle ScholarPubMed
29. McFarland, LV, Elmer, GW, Stamm, WE, Mulligan, ME. Correlation of immunoblot type, enterotoxin production, and cytotoxin production with clinical manifestations of Clostridium difficile infection in cohort of hospitalized patients. Infect Immun 1991;59:24562462.CrossRefGoogle ScholarPubMed