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used to rinse bronchoscopes during reprocessing and resultant contamination of the bronchoscopes themselves. Bronchoscopy clinics, particularly those with high volume


and/or that serve immunocompromised patients, should pro- spectively review BAL cultures to identify unexpected pathogen trends. Our pseudo-outbreak may have been recognized and terminated sooner had routine surveillance of culture results from the bronchoscopy clinic been performed. The molecular data suggests that the pseudo-outbreak likely began earlier than it was clinically recognized. Endoscope-related pseudo-outbreaks, including those caused


by NTM, continue to occur despite standardized procedures for high-level disinfection of endoscopes. Mycobacterium avium and other NTM species, including M. chimaera and M. absces- sus, are known to colonize household and municipal water.10 Based on our findings, we recommend that routine maintenance schedules for AERs and endoscopes be adjusted based on usage and local water quality rather than a fixed time schedule. Additionally, new technologies, such as disposable endoscopes or endoscopes that can be sterilized, are needed to improve the safety of these devices. Our study had some limitations. First, differentiating MAC


clinical infection from colonization is challenging, particularly in lung transplant patients. Therefore, we were not able to calculate incidence rate of MAC infection in the baseline and outbreak periods. However, the significantly lower proportion of patients who received treatment for MAC disease supports the hypothesis that this was a pseudo-outbreak rather than true outbreak. Second, the filter change frequency from quarterly to monthly was instituted for all 3 filter sizes.We did not experiment with varying the timing of only the terminal filter change, nor did we confirm the exact time at which the filters failed. Finally, molecular sequencing was performed on only a convenient sample of isolates from each study period; therefore, we did not determine the true prevalence of the pseudo-epidemic clone in BALs performed throughout the study period. The molecular data show a decrease in recovery of the M. avium pseudo-epidemic clone after the adoption of monthly filter changes. We are unable to determine whether the ongoing recovery of the pseudo-epidemic clone VNTR no. 51 represents ongoing low-level contamination of rinse water or simply indicates that VNTR no. 51 is present in the local municipal water supply and causes colonization or infection in patients when patients are exposed to municipal water via other routes. In conclusion, we describe a pseudo-outbreak of a single clone of M. avium related to failure of the AER rinse water


Jessica L. Seidelman et al


filtration system. Healthcare facilities performing high-volume endoscopy procedures should be aware that AER filters may require replacement based on frequency of use or water quality rather than manufacturers’ recommendations based on time in use.


Acknowledgments. None. Financial support. No financial support was provided relevant to this article.


Conflicts of interest. All authors report no conflicts of interest relevant to this article.


References 1. Kovaleva J, Peters FT, van der Mei HC, Degener JE. Transmission of infection by flexible gastrointestinal endoscopy and bronchoscopy. Clin Microbiol Rev 2013;26:231–254.


2. Wallace RJ Jr, Brown BA, Griffith DE. Nosocomial outbreaks/pseudo- outbreaks caused by nontuberculous mycobacteria. Annu Rev Microbiol 1998;52:453–490.


3. Collins FM. Bactericidal activity of alkaline glutaraldehyde solution against a number of atypical mycobacterial species. J Appl Bacteriol 1986;61:247–251.


4. Falkinham JO 3rd. Nontuberculous mycobacteria from household plumbing of patients with nontuberculous mycobacteria disease. Emerg Infect Dis 2011;17:419–424.


5. CLSI. Laboratory Detection and Identification of Mycobacteria; Approved Guidelines. Wayne, PA: Clinical and Laboratory Standards Institute; 2008.


6. Iakhiaeva E, Howard ST, Elliott BAB, et al. Variable-number tandem- repeat analysis of respiratory and household water biofilm isolates of “Mycobacterium avium subsp. hominissuis” with establishment of a PCR database. J Clin Microbiol 2016;54:891–901.


7. Wallace RJ Jr, Zhang Y, Brown-Elliott BA, et al. Repeat positive cultures in Mycobacterium intracellulare lung disease after macrolide therapy represent new infections in patients with nodular bronchiectasis. J Infect Dis 2002;186:266–273.


8. Rosengarten D, Block C, Hidalgo-Grass C, et al. Cluster of pseudoinfec- tions with Burkholderia cepacia associated with a contaminated washer- disinfector in a bronchoscopy unit. Infect Control Hosp Epidemiol 2010;31:769–771.


9. 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;29:1088–1090.


10. Wallace RJ, Iakhiaeva E, Williams MD, et al. Absence of Mycobacterium intracellulare and presence of Mycobacterium chimaera in household water and biofilm samples of patients in the United States with Mycobacterium avium complex respiratory disease. J Clin Microbiol 2013;51:1747–1752.


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