Hostname: page-component-586b7cd67f-2brh9 Total loading time: 0 Render date: 2024-11-22T06:49:52.105Z Has data issue: false hasContentIssue false

Pseudo-outbreak of Mycobacterium gordonae Following the Opening of a Newly Constructed Hospital at a Chicago Medical Center

Published online by Cambridge University Press:  18 December 2014

Kavitha Prabaker*
Affiliation:
University of Colorado, Aurora, CO, USA
Chethra Muthiah
Affiliation:
Metro Infectious Disease Consultants, Chicago, IL, USA
Mary K. Hayden
Affiliation:
Rush University Medical Center, Chicago, IL, USA
Robert A. Weinstein
Affiliation:
Rush University Medical Center, Chicago, IL, USA Cook County Health and Hospital Systems, Chicago, IL, USA
Jyothirmai Cheerala
Affiliation:
Rush University Medical Center, Chicago, IL, USA
Mary L. Scorza
Affiliation:
Rush University Medical Center, Chicago, IL, USA
John Segreti
Affiliation:
Rush University Medical Center, Chicago, IL, USA
Mary A. Lavin
Affiliation:
Saint Anthony Hospital, Chicago, IL, USA
Barbara A. Schmitt
Affiliation:
Rush University Medical Center, Chicago, IL, USA
Sharon F. Welbel
Affiliation:
Cook County Health and Hospital Systems, Chicago, IL, USA
Kathleen G. Beavis
Affiliation:
University of Chicago, Chicago, IL, USA
Gordon M. Trenholme
Affiliation:
Rush University Medical Center, Chicago, IL, USA
*
Address correspondence to Kavitha Prabaker, MD, 1635 Aurora Ct, Box B163, Aurora, CO 80045 ([email protected]).

Abstract

OBJECTIVE

To identify the source of a pseudo-outbreak of Mycobacterium gordonae

DESIGN

Outbreak investigation.

SETTING

University Hospital in Chicago, Ilinois.

PATIENTS

Hospital patients with M. gordonae-positive clinical cultures.

METHODS

An increase in isolation of M. gordonae from clinical cultures was noted immediately following the opening of a newly constructed hospital in January 2012. We reviewed medical records of patients with M. gordonae-positive cultures collected between January and December 2012 and cultured potable water specimens in new and old hospitals quantitatively for mycobacteria.

RESULTS

Of 30 patients with M. gordonae-positive clinical cultures, 25 (83.3%) were housed in the new hospital; of 35 positive specimens (sputum, bronchoalveolar lavage, gastric aspirate), 32 (91.4%) had potential for water contamination. M. gordonae was more common in water collected from the new vs. the old hospital [147 of 157 (93.6%) vs. 91 of 113 (80.5%), P=.001]. Median concentration of M. gordonae was higher in the samples from the new vs. the old hospital (208 vs. 48 colony-forming units (CFU)/mL; P<.001). Prevalence and concentration of M. gordonae were lower in water samples from ice and water dispensers [13 of 28 (46.4%) and 0 CFU/mL] compared with water samples from patient rooms and common areas [225 of 242 (93%) and 146 CFU/mL, P<.001].

CONCLUSIONS

M. gordonae was common in potable water. The pseudo-outbreak of M. gordonae was likely due to increased concentrations of M. gordonae in the potable water supply of the new hospital. A silver ion-impregnated 0.5-μm filter may have been responsible for lower concentrations of M. gordonae identified in ice/water dispenser samples. Hospitals should anticipate that construction activities may amplify the presence of waterborne nontuberculous mycobacterial contaminants.

Infect Control Hosp Epidemiol 2014;00(0): 1–6

Type
Original Articles
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

These data were presented in part at ID Week 2013, San Francisco, CA, October 2–6, 2013.

References

1. Falkinham, JO 3rd, Norton, CD, LeChevallier, MW. Factors influencing numbers of Mycobacterium avium, Mycobacterium intracellulare, and other mycobacteria in drinking water distribution systems. Appl Envir Microbiol 2001;67:12251231.Google Scholar
2. Mullis, SN, Falkinham, JO 3rd. Adherence and biofilm formation of Mycobacterium avium, Mycobacterium intracellulare and Mycobacterium abscessus to household plumbing materials. J Appl Microbiol 2013;115:908914.Google Scholar
3. Williams, MM, Armbruster, CR, Arduino, MJ. Plumbing of hospital premises is a reservoir for opportunistically pathogenic microorganisms: a review. Biofouling 2013;29:147162.Google Scholar
4. Arnow, PM, Bakir, M, Thompson, K, Bova, JL. Endemic contamination of clinical specimens by Mycobacterium gordonae . Clin Infect Dis 2000;31:472476.Google Scholar
5. Lalande, V, Barbut, F, Varnerot, A, et al. Pseudo-outbreak of Mycobacterium gordonae associated with water from refrigerated fountains. J Hosp Infect 2001;48:7679.Google Scholar
6. Panwalker, AP, Fuhse, E. Nosocomial Mycobacterium gordonae pseudoinfection from contaminated ice machines. Infect Control 1986;7:6770.Google Scholar
7. Stine, TM, Harris, AA, Levin, S, Rivera, N, Kaplan, RL. A pseudoepidemic due to atypical mycobacteria in a hospital water supply. JAMA 1987;258:809811.Google Scholar
8. Tokars, JI, McNeil, MM, Tablan, OC, et al. Mycobacterium gordonae pseudoinfection associated with a contaminated antimicrobial solution. J Clin Microbiol 1990;28:27652769.Google Scholar
9. Fujita, J, Nanki, N, Negayama, K, Tsutsui, S, Taminato, T, Ishida, T. Nosocomial contamination by Mycobacterium gordonae in hospital water supply and super-oxidized water. J Hosp Infect 2002;51:6568.Google Scholar
10. Gubler, JG, Salfinger, M, von Graevenitz, A. Pseudoepidemic of nontuberculous mycobacteria due to a contaminated bronchoscope cleaning machine. Report of an outbreak and review of the literature. Chest 1992;101:12451249.Google Scholar
11. Saukkonen, JJ, Cohn, DL, Jasmer, RM, et al. An official ATS statement: hepatotoxicity of antituberculosis therapy. Am J Respir Crit Care Med 2006;174:935952.Google Scholar
12. Griffith, DE, Aksamit, T, Brown-Elliott, BA, et al. An official ATS/IDSA statement: diagnosis, treatment, and prevention of nontuberculous mycobacterial diseases. Am J Respir Crit Care Med 2007;175:367416.Google Scholar
13. Doebbeling, BN, Wenzel, RP. The epidemiology of Legionella pneumophila infections. Semin Respir Infect 1987;2:206221.Google Scholar
14. Krøjgaard, LH, Krogfelt, KA, Albrechtsen, HJ, Uldum, SA. Cluster of Legionnaires disease in a newly built block of flats, Denmark, December 2008 – January 2009. Euro Surveill 2011;16:19759.Google Scholar
15. Shih, HY, Lin, YE. Efficacy of copper-silver ionization in controlling biofilm- and plankton-associated waterborne pathogens. Appl Environ Microbiol 2010;76:20322035.Google Scholar
16. Gebo, KA, Srinivasan, A, Perl, TM, Ross, T, Groth, A, Merz, WG. Pseudo-outbreak of Mycobacterium fortuitum on a human immunodeficiency virus ward: transient respiratory tract colonization from a contaminated ice machine. Clin Infect Dis 2002;35:3238.CrossRefGoogle ScholarPubMed
17. Williams, MM, Chen, TH, Keane, T, et al. Point-of-use membrane filtration and hyperchlorination to prevent patient exposure to rapidly growing mycobacteria in the potable water supply of a skilled nursing facility. Infect Control Hosp Epidemiol 2011;32:837844.CrossRefGoogle ScholarPubMed