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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

Published online by Cambridge University Press:  02 January 2015

Margaret M. Williams*
Affiliation:
National Center for Emerging and Zoonotic Infectious Diseases, Division of Healthcare Quality Promotion, Centers for Disease Control and Prevention (CDC), Atlanta, Georgia
Tai-Ho Chen
Affiliation:
Office of Surveillance, Epidemiology, and Laboratory Services/Epidemiology Investigative Service Program, CDC, Atlanta, Georgia Pennsylvania Department of Health, Harrisburg, Pennsylvania
Tim Keane
Affiliation:
Environmental Infection Control Consultants, Chalfont, Pennsylvania
Nadege Toney
Affiliation:
National Center for Emerging and Zoonotic Infectious Diseases, Division of Healthcare Quality Promotion, Centers for Disease Control and Prevention (CDC), Atlanta, Georgia
Sean Toney
Affiliation:
National Center for HIV/AIDS, Viral Hepatitis, STD, and TB Prevention, Division of Tuberculosis Elimination, CDC, Atlanta, Georgia
Catherine R. Armbruster
Affiliation:
National Center for Emerging and Zoonotic Infectious Diseases, Division of Healthcare Quality Promotion, Centers for Disease Control and Prevention (CDC), Atlanta, Georgia
W. Ray Butler
Affiliation:
National Center for HIV/AIDS, Viral Hepatitis, STD, and TB Prevention, Division of Tuberculosis Elimination, CDC, Atlanta, Georgia
Matthew J. Arduino
Affiliation:
National Center for Emerging and Zoonotic Infectious Diseases, Division of Healthcare Quality Promotion, Centers for Disease Control and Prevention (CDC), Atlanta, Georgia
*
1600 Clifton Road, MS-C16, Atlanta, GA, 30333 ([email protected])

Abstract

Background.

Healthcare-associated outbreaks and pseudo-outbreaks of rapidly growing mycobacteria (RGM) are frequently associated with contaminated tap water. A pseudo-outbreak of Mycobacterium chelonae–M. abscessus in patients undergoing bronchoscopy was identified by 2 acute care hospitals. RGM was identified in bronchoscopy specimens of 28 patients, 25 of whom resided in the same skilled nursing facility (SNF). An investigation ruled out bronchoscopy procedures, specimen collection, and scope reprocessing at the hospitals as sources of transmission.

Objective.

To identify the reservoir for RGM within the SNF and evaluate 2 water system treatments, hyperchlorination and point-of-use (POU) membrane filters, to reduce RGM.

Design.

A comparative in situ study of 2 water system treatments to prevent RGM transmission.

Setting.

An SNF specializing in care of patients requiring ventilator support.

Methods.

RGM and heterotrophic plate count (HPC) bacteria were examined in facility water before and after hyperchlorination and in a subsequent 24-week assessment of filtered water by colony enumeration on Middlebrook and R2A media.

Results.

Mycobacterium chelonae was consistently isolated from the SNF water supply. Hyperchlorination reduced RGM by 1.5 log10 initially, but the population returned to original levels within 90 days. Concentration of HPC bacteria also decreased temporarily. RGM were reduced below detection level in filtered water, a 3-log10 reduction. HPC bacteria were not recovered from newly installed filters, although low quantities were found in water from 2-week-old filters.

Conclusion.

POU membrane filters may be a feasible prevention measure for healthcare facilities to limit exposure of sensitive individuals to RGM in potable water systems.

Type
Original Articles
Copyright
Copyright © The Society for Healthcare Epidemiology of America 2011

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References

1.Chroneou, A, Zimmerman, SK, Cook, S, et al.Molecular typing of Mycobacterium chelonae isolates from a pseudo-outbreak involving an automated bronchoscope washer. Infect Control Hosp Epidemiol 2008;29(11):10881090.Google Scholar
2.Cox, R, deBorja, K, Bach, MC. A pseudo-outbreak of Mycobacterium chelonae infections related to bronchoscopy. Infect Control Hosp Epidemiol 1997;18(2):136137.Google Scholar
3.Kressel, AB, Kidd, F. Pseudo-outbreak of Mycobacterium chelonae and Methylobacterium mesophilicum caused by contamination of an automated endoscopy washer. Infect Control Hosp Epidemiol 2001;22(7):414418.CrossRefGoogle ScholarPubMed
4.Phillips, MS, von Reyn, CF. Nosocomial infections due to non-tuberculous mycobacteria. Clin Infect Dw200T;33(8):13631374.Google Scholar
5.Wallace, RJ Jr, Brown, BA, Griffith, DE. Nosocomial outbreaks/pseudo-outbreaks caused by nontuberculous mycobacteria. Annu Rev Microbiol 1998;52:453490.Google Scholar
6.Griffith, DE, Aksamit, T, Brown-Elliott, BA, et al.An official ATS/IDSA statement: diagnosis, treatment and prevention of non-tuberculous mycobacterial diseases. Am J Respir Crit Care Med 2007;175:367416.Google Scholar
7.Chen, T, Dettinger, L, Waller, K, et al.Investigation of Mycobacterium chelonae/abscessus in three healthcare facilities: Pennsylvania 2002-2006. Poster presented at: 56th Annual Epidemic Intelligence Service Conference, 2007; Atlanta, GA.Google Scholar
8.Arnow, PM, Bakir, M, Thompson, K, Bova, JL. Endemic contamination of clinical specimens by Mycobacterium gordonae. Clin Infect Dis 2000;31(2):472476.CrossRefGoogle ScholarPubMed
9.Bettiker, RL, Axelrod, PI, Fekete, T, et al.Delayed recognition of a pseudo-outbreak of Mycobacterium terrae. Am J Infect Control 2006;34(6):343347.CrossRefGoogle ScholarPubMed
10.Blossom, DB, Alelis, KA, Chang, DC, et al.Pseudo-outbreak of Mycobacterium abscessus infection caused by laboratory contamination. Infect Control Hosp Epidemiol 2008;29(1):5762.Google Scholar
11.El Sahly, HM, Septimus, E, Soini, H, et al.Mycobacterium simiae pseudo-outbreak resulting from a contaminated hospital water supply in Houston, Texas. Clin Infect Dis 2002;35(7):802807.CrossRefGoogle ScholarPubMed
12.Esteban, J, Fernández-Roblas, R, Ortiz, A, García-Cía, JI. Pseudo-outbreak of Mycobacterium gordonae. usefulness of randomly amplified polymorphic DNA analysis to assess the clonality of the isolates. Clin Microbiol Infect 2006;12(7):677679.Google Scholar
13.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(1):3238.Google Scholar
14.Lai, KK, Brown, BA, Westerling, JA, Fontecchio, SA, Zhang, Y, Wallace, RJ Jr.Long-term laboratory contamination by Mycobacterium abscessus resulting in two pseudo-outbreaks: recognition with use of random amplified polymorphic DNA (RAPD) polymerase chain reaction. Clin Infect Dis 1998;27(1):169175.Google Scholar
15.Lalande, V, Barbut, F, Varnerot, A, et al.Pseudo-outbreak of Mycobacterium gordonae associated with water from refrigerated fountains. J Hosp Infect 2001;48(1):7679.Google Scholar
16.Maloney, S, Welbel, S, Daves, B, et al.Mycobacterium abscessus pseudo-infection traced to an automated endoscope washer: utility of epidemiologic and laboratory investigation.J Infect Dis 1994;169(5):11661169.Google Scholar
17.Ortiz, A, Esteban, J, Zamora, N. Molecular identification by random amplified polymorphic DNA analysis of a pseudo-outbreak of Mycobacterium fortuitum due to cross-contamination of clinical samples. J Med Microbiol 2007;56(6):871872.Google Scholar
18.Sniadack, DH, Ostroff, SM, Karlix, MA, et al.A nosocomial pseudo-outbreak of Mycobacterium xenopi due to a contaminated potable water supply: lessons in prevention. Infect Control Hosp Epidemiol 1993;14(11):636641.Google Scholar
19.Wang, SH, Pancholi, P, Stevenson, K, et al.Pseudo-outbreak of “Mycobacterium parajfinicum” infection and/or colonization in a tertiary care medical center. Infect Control Hosp Epidemiol 2009;30(9):848853.Google Scholar
20.Eaton, AD, Clesceri, LS, Rice, EW, Greenberg, AE, eds. Standard Methods for the Examination of Water and Wastewater. 21st ed. Washington, DC: American Public Health Association; 2005.Google Scholar
21.Kent, PT, Kubica, GRPublic Health Laboratory: A Guide for the Level III Laboratory. US Department of Health and Human Services publication no. 86-8230. Atlanta, GA: Centers for Disease Control and Prevention; 1985.Google Scholar
22.Butler, WR, Floyd, MM, Silcox, V, et al.Standardized Method for HPLC Identification of Mycobacteria. Atlanta, GA: Centers for Disease Control and Prevention; 1996. http://www.cdc.gov/nci-dod/publications/hplcpdf. Accessed July 14, 2011.Google Scholar
23.Butler, WR, Guthertz, LS. Mycolic acid analysis by high-performance liquid chromatography for identification of Mycobacterium species. Clin Microbiol Rev 2001;14:704726.Google Scholar
24.Telenti, A, Marchesi, F, Balz, M, Bally, F, Bottger, EC, Bodmer, T. Rapid identification of mycobacteria to the species level by polymerase chain reaction and restriction enzyme analysis. J Clin Microbiol 1993;31(2):175178.Google Scholar
25.Häfner, B, Haag, H, Geiss, H, Nolte, O. Different molecular methods for the identification of rarely isolated non-tuberculous mycobacteria and description of new hsp65 restriction fragment length polymorphism patterns. Mol Cell Probes 2004;18(1):5965.Google Scholar
26.Adékambi, T, Colson, P, Drancourt, M. rpoB-based identification of nonpigmented and late-pigmenting rapidly growing mycobacteria. J Clin Microbiol 2003;41:56995708.CrossRefGoogle ScholarPubMed
27.Adékambi, T, Drancourt, M. Dissection of phylogenetic relationships among 19 rapidly growing Mycobacterium species by 16S rRNA, hsp65, recA and rpoB gene sequencing. Int J Syst Evol Microbiol 2004;54:20952105.Google Scholar
28.US Environmental Protection Agency. The Safe Water Drinking Act, 1974 (amended in 1986 and 1996). Current regulations available at http://water.epa.gov/drinWcontaminants/index.cfrn. Accessed November 17, 2010.Google Scholar
29.Manuel, CM, Nunes, OC, Melo, LEDynamics of drinking water biofilm in flow/non-flow conditions. Wat Res 2010;41(3):551562.Google Scholar
30.Makin, T, Hart, CA. The efficacy of control measures for eradicating legionellae in showers. J Hosp Inf 1990;16:17.Google Scholar
31.Srinivasan, A, Bova, G, Ross, T, et al.A 17-month evaluation of a chlorine dioxide water treatment system to control Legionella species in a hospital water supply. Infect Control Hosp Epidemiol 2003;24:575579.Google Scholar
32.LeDantec, C, Duguet, JP, Montiel, A, Dumoutier, N, Dubrou, S, Vincent, V. Chlorine disinfection of atypical mycobacteria isolated from a water distribution system. Appi Environ Microbiol 2002;68:10251032.Google Scholar
33.Norton, CD, LeChevallier, M, Falkinham, JO. Survival of Mycobacterium avium in a model distribution system. Wat Res 2004;38:14571466.Google Scholar
34.Pepper, IL, Rusin, P, Quintanar, DR, Haney, C, Josephson, KL, Gerba, CP. Tracking the concentration of heterotrophic plate count bacteria from the source to the consumer's tap. Int J Food Miaobiol 2004;92:289295.Google Scholar
35.Covert, TC, Rodgers, MR, Reyes, AL, Stelma, GN Jr.Occurrence of nontuberculous mycobacteria in environmental samples. Appi Environ Microbiol 1999;65:24922496.CrossRefGoogle ScholarPubMed
36.Howard, ST, Rhoades, E, Recht, J, et al.Spontaneous reversion of Mycobacterium abscessus from a smooth to a rough morphotype is associated with reduced expression of glycopepti-dolipid and reacquisition of an invasive phenotype. Microbiology 2006;152:15811590.CrossRefGoogle ScholarPubMed
37.Gomila, M, Ramirez, A, Gaseo, J, Lalucat, J. Mycobacterium llatz-erense sp. nov., a facultatively autotrophic, hydrogen-oxidizing bacterium isolated from haemodialysis water. Int J Syst Evol Mkrobiol 2008;58(12):27692773.Google Scholar
38.Cooksey, RC, Jhung, MA, Yakrus, MA, et al.Multiphasic approach reveals genetic diversity of environmental and patient isolates of Mycobacterium mucogenicum and Mycobacterium phocaicum associated with an outbreak of bacteremias at a Texas hospital. Appi Environ Microbiol 2008;74(8):24802487.Google Scholar
39.LaBombardi, VJ, O'Brien, AM, Kislak, JW. Pseudo-outbreak of Mycobacterium fortuitum due to contaminated ice machines. Am J Infect Control 2002;30(3):184186.Google Scholar
40.Manangan, LP, Anderson, RL, Arduino, MJ, Bond, WW. Sanitary care and maintenance of ice-storage chests and ice-making machines in health care facilities. Am J Infect Control 1998;26:111112.Google Scholar