Pseudo-outbreak of Stenotrophomonas maltophilia due to contamination of bronchoscope

We noticed an abrupt increase in the isolation of Stenotrophomonas maltophilia from bronchoalveolar lavage (BAL) specimens collected at Chosun University Hospital. We performed surveillance cultures in order to identify the source of what appeared to be a pseudo-outbreak. To investigate a possible n...

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Veröffentlicht in:Taehan Chindan Kŏmsa Ŭihakhoe chi 2007-06, Vol.27 (3), p.205-209
Hauptverfasser: Ahn, Gyun Yeol, Yu, Feng Nan, Jang, Sook Jin, Kim, Dong-Min, Park, Geon, Moon, Dae Soo, Park, Young Jin
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container_title Taehan Chindan Kŏmsa Ŭihakhoe chi
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creator Ahn, Gyun Yeol
Yu, Feng Nan
Jang, Sook Jin
Kim, Dong-Min
Park, Geon
Moon, Dae Soo
Park, Young Jin
description We noticed an abrupt increase in the isolation of Stenotrophomonas maltophilia from bronchoalveolar lavage (BAL) specimens collected at Chosun University Hospital. We performed surveillance cultures in order to identify the source of what appeared to be a pseudo-outbreak. To investigate a possible nosocomial outbreak of S. maltophilia, we performed culture of 11 environmental specimens obtained from a bronchoscopy room and two bronchoscopes. Pulsed-field gel electrophoresis (PFGE) was used to examine the genetic relatedness among the strains of S. maltophilia recovered from BAL specimens of 3 patients and 1 environmental sample, as well as 9 unrelated strains of S. maltophilia as a control. During a 7 day-period in March 2006, S. maltophilia was isolated from the BAL specimens of 7 of 13 (54%) patients, compared to only 5 of 188 (2.6%) patients during the 6-month period prior to that period. S. maltophilia was isolated from 1 of the 11 environmental samples, which was obtained from a fiberoptic bronchoscope suction channel. All 7 patient isolates and one environmental isolate exhibited similar antibiotic susceptibility patterns. PFGE analysis of the genomic DNA from epidemic strains demonstrated an identical banding pattern, whereas each of epidemiologically unrelated strains showed a unique electrophoretic pattern. Apparently one of the hospital bronchoscopes became contaminated with S. maltophilia during a bronchoscopic procedure. It is likely that subsequent specimen contamination occurred because the bronchoscope had been inadequately cleaned and disinfected. The pseudo-outbreak was controlled successfully by removing the source of infection.
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PFGE analysis of the genomic DNA from epidemic strains demonstrated an identical banding pattern, whereas each of epidemiologically unrelated strains showed a unique electrophoretic pattern. Apparently one of the hospital bronchoscopes became contaminated with S. maltophilia during a bronchoscopic procedure. It is likely that subsequent specimen contamination occurred because the bronchoscope had been inadequately cleaned and disinfected. 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PFGE analysis of the genomic DNA from epidemic strains demonstrated an identical banding pattern, whereas each of epidemiologically unrelated strains showed a unique electrophoretic pattern. Apparently one of the hospital bronchoscopes became contaminated with S. maltophilia during a bronchoscopic procedure. It is likely that subsequent specimen contamination occurred because the bronchoscope had been inadequately cleaned and disinfected. 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We performed surveillance cultures in order to identify the source of what appeared to be a pseudo-outbreak. To investigate a possible nosocomial outbreak of S. maltophilia, we performed culture of 11 environmental specimens obtained from a bronchoscopy room and two bronchoscopes. Pulsed-field gel electrophoresis (PFGE) was used to examine the genetic relatedness among the strains of S. maltophilia recovered from BAL specimens of 3 patients and 1 environmental sample, as well as 9 unrelated strains of S. maltophilia as a control. During a 7 day-period in March 2006, S. maltophilia was isolated from the BAL specimens of 7 of 13 (54%) patients, compared to only 5 of 188 (2.6%) patients during the 6-month period prior to that period. S. maltophilia was isolated from 1 of the 11 environmental samples, which was obtained from a fiberoptic bronchoscope suction channel. All 7 patient isolates and one environmental isolate exhibited similar antibiotic susceptibility patterns. PFGE analysis of the genomic DNA from epidemic strains demonstrated an identical banding pattern, whereas each of epidemiologically unrelated strains showed a unique electrophoretic pattern. Apparently one of the hospital bronchoscopes became contaminated with S. maltophilia during a bronchoscopic procedure. It is likely that subsequent specimen contamination occurred because the bronchoscope had been inadequately cleaned and disinfected. The pseudo-outbreak was controlled successfully by removing the source of infection.</abstract><cop>Korea (South)</cop><pmid>18094577</pmid><doi>10.3343/kjlm.2007.27.3.205</doi><tpages>5</tpages></addata></record>
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source KoreaMed Synapse; MEDLINE; KoreaMed Open Access; EZB-FREE-00999 freely available EZB journals; Alma/SFX Local Collection
subjects Aged
Aged, 80 and over
Bronchoalveolar Lavage Fluid - microbiology
Bronchoscopes - microbiology
Disease Outbreaks
Electrophoresis, Gel, Pulsed-Field
Equipment Contamination
Gram-Negative Bacterial Infections - diagnosis
Gram-Negative Bacterial Infections - epidemiology
Gram-Negative Bacterial Infections - transmission
Humans
Male
Microbial Sensitivity Tests
Middle Aged
Stenotrophomonas maltophilia - genetics
Stenotrophomonas maltophilia - isolation & purification
title Pseudo-outbreak of Stenotrophomonas maltophilia due to contamination of bronchoscope
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