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An outbreak of Pseudomonas aeruginosa infections associated with flexible bronchoscopes
Arjun Srinivasan1, Linda L Wolfenden, Xiaoyan Song
1Department of Hospital Epidemiology and Infection Control, Johns Hopkins Medical Institutions, Baltimore, Md, USA.
Background:
Endoscopes, including bronchoscopes, are the medical devices most frequently associated with outbreaks of nosocomial infections. We investigated an outbreak of Pseudomonas aeruginosa infections after bronchoscopic procedures.
Methods:
Microbiologic results were reviewed to determine the rates of recovery of P. aeruginosa from bronchoalveolar-lavage specimens. Environmental samples from endoscopes and the endoscopy suite were cultured. Medical records were reviewed to identify infections in the 14 days after a bronchoscopy.
Results:
The rate of recovery of P. aeruginosa from bronchoalveolar-lavage specimens obtained with use of endoscopy-suite bronchoscopes increased from 10.4 percent at base line to 31.0 percent during the outbreak (relative risk, 2.97; 95 percent confidence interval, 2.28 to 3.90). Cultures of samples from three bronchoscopes grew P. aeruginosa, whereas cultures of samples from the environment, instrument-cleaning machines, and gastrointestinal endoscopes did not. The three bronchoscopes had been part of a nationwide recall. A total of 414 patients underwent bronchoscopy during the outbreak, and there were 48 respiratory tract and bloodstream infections among 39 of these patients (9.4 percent). In 32 infections (66.7 percent), P. aeruginosa was confirmed as a potentially causative organism. Exposure to a potentially contaminated bronchoscope may have had a role in the death of three patients. The rate of recovery of P. aeruginosa returned to base line after the instruments were removed from service.
Conclusions:
This large outbreak of P. aeruginosa infections related to bronchoscopy was apparently caused by a loose biopsy-port cap in the bronchoscopes. Instrument safety and surveillance methods for bronchoscopy must be improved, and better recall procedures are needed for medical devices.
Insights
A Pseudomonas aeruginosa outbreak linked to bronchoscopes caused increased infections and deaths. Contaminated bronchoscopes, possibly due to a faulty cap, led to 9.4% of patients developing infections. Improved device safety and recalls are crucial.
Area of Science:
- Infectious Diseases
- Medical Device Safety
- Epidemiology
Background:
- Endoscopes, particularly bronchoscopes, are frequently implicated in nosocomial infection outbreaks.
- This study investigated a specific outbreak of Pseudomonas aeruginosa infections following bronchoscopic procedures.
Purpose of the Study:
- To investigate an outbreak of Pseudomonas aeruginosa infections associated with bronchoscopy.
- To identify the source and contributing factors of the outbreak.
Main Methods:
- Reviewed microbiologic data to assess P. aeruginosa recovery rates from bronchoalveolar-lavage specimens.
- Cultured environmental samples from endoscopes and the endoscopy suite.
- Examined medical records to identify patient infections post-bronchoscopy.
Main Results:
- P. aeruginosa recovery rates significantly increased during the outbreak (31.0% vs. 10.4% baseline).
- Three bronchoscopes tested positive for P. aeruginosa; these were part of a nationwide recall.
- 9.4% of patients (39/414) developed infections, with P. aeruginosa confirmed in 66.7% of cases. Three deaths were potentially linked to contaminated bronchoscopes.
Conclusions:
- A loose biopsy-port cap on bronchoscopes was the likely cause of this large P. aeruginosa outbreak.
- Enhanced instrument safety, surveillance, and medical device recall procedures are necessary for bronchoscopy.
- Removing contaminated instruments returned P. aeruginosa recovery rates to baseline.
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