Skip directly to local search Skip directly to A to Z list Skip directly to navigation Skip directly to site content Skip directly to page options
CDC Home

Volume 16, Number 5—May 2010

Dispatch

Multihospital Outbreak of Clostridium difficile Infection, Cleveland, Ohio, USA

Robin L.P. Jump, Michelle M. Riggs, Ajay K. Sethi, Michael J. Pultz, Tracie Ellis-Reid, William Riebel, Dale N. Gerding, Robert A. Salata, and Curtis J. DonskeyComments to Author 
Author affiliations: University Hospitals of Cleveland, Cleveland, Ohio, USA (R.L.P. Jump, R.A. Salata); Cleveland Veterans Affairs Medical Center, Cleveland (M.M. Riggs, M.J. Pultz, T. Ellis-Reid, C.J. Donskey); Case Western Reserve University, Cleveland (A.K. Sethi); Lakewood Hospital, Lakewood, Ohio, USA (W. Riebel); Hines Veterans Affairs Hospital, Hines, Illinois, USA (D.N. Gerding); Loyola University Chicago Stritch School of Medicine, Maywood, Illinois, USA (D.N. Gerding)

Suggested citation for this article

Abstract

To determine whether a multihospital Clostridium difficile outbreak was associated with epidemic strains and whether use of particular fluoroquinolones was associated with increased infection rates, we cultured feces from C. difficile–infected patients. Use of fluoroquionolones with enhanced antianaerobic activity was not associated with increased infection rates.

Recent outbreaks of Clostridium difficile infection have been attributed to the emergence of an epidemic strain characterized as North American pulsed-field gel electrophoresis type 1 (NAP1) or restriction endonuclease assay group BI (1,2). Fluoroquinolone resistance is a hallmark of epidemic C. difficile isolates (1), and fluoroquinolone use has been associated with C. difficile infection (29). Because the C-8 methoxy fluoroquinolones gatifloxacin and moxifloxacin have enhanced antianaerobic activity, they might promote C. difficile infection to a greater degree than ciprofloxacin and levofloxacin (10). In 3 studies, substitution of gatifloxacin or moxifloxacin for levofloxacin was associated with an increase in C. difficile infection (6,8,9); in 2 of the 3 studies, a formulary change back to levofloxacin was associated with reduced C. difficile infection (6,9). However, ciprofloxacin and levofloxacin also have been associated with C. difficile infection (25,7).

Beginning in 2002, outbreaks of C. difficile infection occurred in several hospitals in the Cleveland, Ohio, USA, area. In response, the Ohio Department of Health (ODH) made C. difficile infection a reportable disease in 2006. One objective of the current study was to examine the magnitude of the outbreaks in Cuyahoga County, which comprises Cleveland and the surrounding area, and to determine whether the outbreaks were associated with epidemic BI/NAP1strains. A second objective was to examine whether use of gatifloxacin and/or moxifloxacin was associated with increased rates of C. difficile infection in healthcare facilities and to assess whether outbreaks correlated with formulary changes in fluoroquinolones.

The Study

We used the ODH website (www.odh.state.oh.us) to obtain rates (cases/10,000 patient-days) of initial C. difficile infections during January–December 2006 for the 22 hospitals in Cuyahoga County. All healthcare facilities in Ohio were required to submit C. difficile infection rates by using a standardized method of reporting. An initial case was defined as a first positive laboratory diagnostic test for C. difficile, pseudomembranes on endoscopy, or confirmatory histologic features from surgical or autopsy specimen. An infection that occurred >6 months after a previous infection was classified as an initial infection.

For a subset of 5 hospitals, up to 20 consecutive stool samples from individual patients with C. difficile infection were cultured for C. difficile (11). C. difficile isolates were tested for in vitro cytotoxin production and moxifloxacin susceptibility and analyzed for binary toxin gene cdtB and partial deletions of the tcdC gene (1113). Molecular typing was performed by using PCR ribotyping (11). The 5 hospitals were 1 community hospital, 3 tertiary care facilities, and 1 Veterans Affairs hospital. Three of the hospitals had experienced large outbreaks of C. difficile infection in 2002–2003 (i.e., their C. difficile incidence doubled and their peak incidence was >20 cases per 1,000 discharges); the other 2 reported an increase in the proportion of cases that were fulminant. The infection control departments of each institution provided information about C. difficile infection rates, fluoroquinolones on formulary, and infection control measures for C. difficile during January 2000–December 2006.

Rates of C. difficile infection for 2006 were compared among hospitals with moxifloxacin or gatifloxacin versus those with levofloxacin on formulary as primarily fluoroquinolones used to treat respiratory infections. In addition, for 2 hospitals in the molecular typing analysis that had a formulary change from 1 respiratory fluoroquinolone to another, we used Poisson analysis to compare rates of C. difficile infection during the 12 months before and after the formulary change, with a lag of 1 month after the change. We analyzed data using SPSS statistical software version 10.0 (SPSS Inc., Chicago, IL, USA) and STATA 9.1 (StataCorp, College Station, TX, USA).

For the 18 adult acute-care hospitals and 4 long-term acute-care (LTAC) facilities in Cuyahoga County, the median C. difficile infection rate in 2006 was 7.3 (range 4.2–63.1 cases/10,000 patient-days). The highest rates were observed in 2 LTAC facilities. Six facilities (3 acute care hospitals and 3 LTACs) had higher C. difficile infection rates than did each of the 5 hospitals in the molecular typing analysis.

A total of 64 toxigenic C. difficile isolates were cultured from feces samples obtained from 5 hospitals. Features of 42 (66%) isolates were consistent with epidemic BI/NAP1 strains (range 55%–83% for each facility), including amplification of the binary toxin gene cdtB and partial deletions in tcdC and resistance to moxifloxacin (MICs >32 µg/mL). By PCR ribotyping, we observed a characteristic banding pattern for isolates with features of the epidemic strain; 6 isolates with this banding pattern were confirmed as BI strains in the laboratory of D.G.

Of the 22 facilities, 8 used moxifloxacin as the primary respiratory fluoroquinolone, 13 used levofloxacin, and 1 did not have a respiratory fluoroquinolone on formulary. The C. difficile infection rate did not differ between facilities with levofloxacin (8.5 cases/10,000 patient-days, 95% confidence interval [CI] 7.8–9.3) and moxifloxacin (8.5 cases/10,000 patient-days, 95% CI 7.8–9.2) on formulary (p = 1) (Table). The facility that did not have a respiratory fluoroquinolone on formulary had a lower rate of C. difficile infection than the median rates for facilities that used levofloxacin or moxifloxacin. However, 8 facilities had lower C. difficile infection rates than did this institution.

Figure

Thumbnail of Rates of Clostridium difficile infection for hospital 1 (A) and hospital 2 (B). Arrows indicate the timing of the formulary changes in fluoroquinolone antimicrobial drugs.

Figure. Rates of Clostridium difficile infection for hospital 1 (A) and hospital 2 (B). Arrows indicate the timing of the formulary changes in fluoroquinolone antimicrobial drugs.

Two of the 5 hospitals in the molecular typing analysis changed their formulary fluoroquinolones during the study period (Figure). Both hospitals made formulary changes from levofloxacin to gatifloxacin; however, the increase in C. difficile infection rates preceded the formulary change in each hospital. C. difficile infection rates did not differ significantly in the 12 months before and after the change from levofloxacin to gatifloxacin (relative risk [RR] 1.0, 95% CI 0.97–0.86; p = 0.973). For hospital 2 (Figure, panel B), a subsequent formulary change from gatifloxacin to levofloxacin was associated with a reduction in C. difficile infection (RR 0.59, 95% CI 0.51–0.70; p<0.001); an intervention to improve environmental cleaning with a 10% bleach solution occurred at the time of the formulary change.

Conclusions

Our findings provide further evidence that emergence of epidemic NAP1/BI strains in a geographic region may be associated with large multihospital outbreaks of C. difficile infection. Before the ODH decision to require mandatory reporting, many area hospitals were either not collecting surveillance data about C. difficile infection or were reluctant to share their rates. Therefore, we believe that mandatory public reporting of C. difficile infection rates provided a valuable tool to examine the full magnitude of the outbreaks and an incentive for hospitals with high rates to increase efforts to control infection. One area hospital recently reported that the ODH database underestimated the incidence of C. difficile infection (14), but this observation does not affect our conclusions because all facilities used the same surveillance definitions. Our findings do not support the hypothesis that use of moxifloxacin or gatifloxacin is associated with higher rates of C. difficile infection than is use of levofloxacin or ciprofloxacin.

Our analysis of formulary fluoroquinolones and C. difficile infection has several limitations. First, data on the amount of the fluoroquinolones used in the hospitals were not available. Second, analysis of hospital formularies does not account for the effects of fluoroquinolones used in long-term care facilities and among outpatients. Third, we did not assess confounding factors, such as use of other classes of antimicrobial drugs and differing patient populations. Finally, studies that evaluate group-level effects may not reflect the biological effects at the individual-patient level. Additional studies are needed to evaluate the risk for C. difficile infection associated with different fluoroquinolones.

Dr Jump is an infectious diseases fellow at University Hospitals in Cleveland, Ohio. Her research interests include intestinal immunology and C. difficile.

Acknowledgment

This study was supported by an Advanced Research Career Development Award from the Department of Veterans Affairs to C.J.D. Restriction endonuclease assay typing was provided by Susan Sambol under a Department of Veterans Affairs Research Service grant to D.N.G.

References

  1. McDonald LC, Killgore GE, Thompson A, Owens RC, Kazakova SV, Sambol SP, An epidemic, toxin gene–variant strain of Clostridium difficile.N Engl J Med. 2005;353:243341. DOIPubMed
  2. Loo VG, Poirier L, Miller MA, Oughton M, Libman MD, Michaud S, A predominantly clonal multi-institutional outbreak of Clostridium difficile–associated diarrhea with high morbidity and mortality.N Engl J Med. 2005;353:24429. DOIPubMed
  3. Muto CA, Pokrywka M, Shutt K, Mendelsohn AB, Nouri K, Posey K, A large outbreak of Clostridium difficile–associated disease with an unexpected proportion of deaths and colectomies at a teaching hospital following increased fluoroquinolone use.Infect Control Hosp Epidemiol. 2005;26:27380. DOIPubMed
  4. Yip C, Loeb M, Salama S, Moss L, Olde J. Quinolone use as a risk factor for nosocomial Clostridium difficile–associated diarrhea.Infect Control Hosp Epidemiol. 2001;22:5725. DOIPubMed
  5. McCusker ME, Harris AD, Perencevich E, Roghmann MC. Fluoroquinolone use and Clostridium difficile–associated diarrhea.Emerg Infect Dis. 2003;9:7303.PubMed
  6. Gaynes R, Rimland D, Killum E, Lowery K, Johnson TM, Kilgore G, Outbreak of Clostridium difficile infection in a long-term care facility: association with gatifloxacin use.Clin Infect Dis. 2004;28:6405. DOIPubMed
  7. Pepin J, Saheb N, Coulombe M, Alary ME, Corriveau MP, Authier S, Emergence of fluoroquinolones as the predominant risk factor for Clostridium difficile–associated diarrhea: a cohort study during an epidemic in Quebec.Clin Infect Dis. 2005;41:125460. DOIPubMed
  8. Biller P, Shank B, Lind L, Brennan M, Tkatch L, Killgore G, Moxifloxacin therapy as a risk factor for Clostridium difficile–associated disease during an outbreak: attempts to control a new epidemic strain.Infect Control Hosp Epidemiol. 2007;28:198201. DOIPubMed
  9. von Baum H, Sigge A, Bommer M, Kern WV, Marre R, Dohner H, Moxifloxacin prophylaxis in neutropenic patients.J Antimicrob Chemother. 2007;58:8914. DOIPubMed
  10. Adams DA, Riggs MM, Donskey CJ. Effect of fluoroquinolone treatment on growth of and toxin production by epidemic and non-epidemic Clostridium difficile strains in the cecal contents of mice.Antimicrob Agents Chemother. 2007;51:26748. DOIPubMed
  11. Al-Nassir W, Riggs MM, Bobulsky G, Donskey CJ. A comparison of clinical and microbiological response to therapy of Clostridium difficile infection with metronidazole versus vancomycin.Clin Infect Dis. 2008;47:5662. DOIPubMed
  12. Terhes G, Urban E, Soki J, Hamid KA, Nagy E. Community-acquired Clostridium difficile diarrhea caused by binary toxin, toxin A, and toxin B gene-positive isolates in Hungary.J Clin Microbiol. 2004;42:43168. DOIPubMed
  13. Spigaglia P, Mastrantonio P. Molecular analysis of the pathogenicity locus and polymorphism in the putative negative regulator of toxin production (TcdC) among Clostridium difficile isolates.J Clin Microbiol. 2002;40:34705. DOIPubMed
  14. Fraser T, Fatica C, Gordon SM. Public reporting of Clostridium difficile associated diarrhea (CDAD): in-house vs. mandated definitions. In: Abstracts of the 17th Annual Scientific Meeting of The Society for Healthcare Epidemiology of America; Baltimore, Maryland; 2007 April 14–17; Abstract 168. Arlington (VA): Society for Healthcare Epidemiology of America; 2007.

Figure

Table

Suggested citation for this article: Jump RLP, Riggs MM, Sethi AK, Pultz MJ, Ellis-Reid T, Riebel W, et al. Multihospital outbreak of Clostridium difficile infection, Cleveland, Ohio, USA. Emerg Infect Dis [serial on the Internet]. 2010 May [date cited]. http://wwwnc.cdc.gov/eid/article/16/5/07-1606.htm

DOI: 10.3201/eid1605.071606

Top of Page

Table of Contents – Volume 16, Number 5—May 2010

Comments to the Authors

Please use the form below to submit correspondence to the authors or contact them at the following address:

Curtis J. Donskey, Infectious Diseases Section, Cleveland Veterans Affairs Medical Center, 10701 East Blvd, Cleveland, OH 44106, USA





characters(s) remaining.

Comment submitted successfully, thank you for your feedback.

Comments to the EID Editors

Please contact the EID Editors via our Contact Form.

 

Past Issues

Select a Past Issue:

Art in Science - Selections from Emerging Infectious Diseases
Now available for order



CDC 24/7 – Saving Lives, Protecting People, Saving Money. Learn More About How CDC Works For You…

USA.gov: The U.S. Government's Official Web PortalDepartment of Health and Human Services
Centers for Disease Control and Prevention   1600 Clifton Rd. Atlanta, GA 30333, USA
800-CDC-INFO (800-232-4636) TTY: (888) 232-6348 - Contact CDC–INFO