J. Broertjes , E.C. van Overbeek , T. Ten Doesschate , K. Slieker , E. Hazenberg , S.P.M. Lutgens , E. Kolwijck , A.C.A.P. Leenders , P.C. Wever
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Recently, we have had three unexpected cases in which <em>Brucella</em> spp. were cultured at our clinical microbiology laboratory: one <em>Brucella canis</em> case and two <em>Brucella melitenis</em> cases. The <em>B. canis</em> and the first <em>B. melitenis</em> cases prompted the introduction of a biosafety software pop-up, which is presented in this paper.</p></div><div><h3>Methods</h3><p>Here, we describe the two <em>B. melitensis</em> cases and the introduction of a biosafety pop-up. The software pop-up parameters are a time-to-positivity (TTP) of more than 48 h, in an aerobic blood culture bottle, and a Gram stain appearance as Gram-negative bacteria. The software pop-up warns the technician through the laboratory information system (LIS) to further process the specimen in the Class 2 biological safety cabinet. To assess the number of false-positive pop-ups we can expect and resulting additional workload, we retrospectively analyzed laboratory data from the last seven years.</p></div><div><h3>Results</h3><p>The biosafety pop-up prevented laboratory exposure in the second <em>B. melitensis</em> case. Based on the retrospective analysis of laboratory data, we estimated the resulting additional workload of implementation of the biosafety pop-up to be less than one blood culture bottle per week on average to be processed in a Class 2 biological safety cabinet.</p></div><div><h3>Conclusion</h3><p>Our experience demonstrates that implementation of the biosafety software pop-up can reduce the risk of laboratory exposure to <em>Brucella</em> spp. This intervention provides a feasible approach even in a setting where <em>Brucella</em> spp. are normally only encountered every few years.</p></div>","PeriodicalId":48593,"journal":{"name":"Microbial Risk Analysis","volume":null,"pages":null},"PeriodicalIF":3.0000,"publicationDate":"2024-05-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2352352224000185/pdfft?md5=74593f8378bd026a2ca07c1f5a2680aa&pid=1-s2.0-S2352352224000185-main.pdf","citationCount":"0","resultStr":"{\"title\":\"Implementation of a biosafety software pop-up after two Brucella laboratory exposures\",\"authors\":\"J. 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The <em>B. canis</em> and the first <em>B. melitenis</em> cases prompted the introduction of a biosafety software pop-up, which is presented in this paper.</p></div><div><h3>Methods</h3><p>Here, we describe the two <em>B. melitensis</em> cases and the introduction of a biosafety pop-up. The software pop-up parameters are a time-to-positivity (TTP) of more than 48 h, in an aerobic blood culture bottle, and a Gram stain appearance as Gram-negative bacteria. The software pop-up warns the technician through the laboratory information system (LIS) to further process the specimen in the Class 2 biological safety cabinet. To assess the number of false-positive pop-ups we can expect and resulting additional workload, we retrospectively analyzed laboratory data from the last seven years.</p></div><div><h3>Results</h3><p>The biosafety pop-up prevented laboratory exposure in the second <em>B. melitensis</em> case. 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Implementation of a biosafety software pop-up after two Brucella laboratory exposures
Introduction
Brucellosis is rare in non-endemic countries where it mainly occurs as an imported or travel-related disease. In rare cases, Brucella species (spp.) are present in clinical specimens processed by clinical microbiology laboratories. These pathogens pose a risk to laboratory technicians, due to the high virulence, a low-infectious dose and ease of aerosol formation. Due to the low incidence in non-endemic countries, clinical samples are routinely processed on laboratory benches outside laminar flow cabinets. Recently, we have had three unexpected cases in which Brucella spp. were cultured at our clinical microbiology laboratory: one Brucella canis case and two Brucella melitenis cases. The B. canis and the first B. melitenis cases prompted the introduction of a biosafety software pop-up, which is presented in this paper.
Methods
Here, we describe the two B. melitensis cases and the introduction of a biosafety pop-up. The software pop-up parameters are a time-to-positivity (TTP) of more than 48 h, in an aerobic blood culture bottle, and a Gram stain appearance as Gram-negative bacteria. The software pop-up warns the technician through the laboratory information system (LIS) to further process the specimen in the Class 2 biological safety cabinet. To assess the number of false-positive pop-ups we can expect and resulting additional workload, we retrospectively analyzed laboratory data from the last seven years.
Results
The biosafety pop-up prevented laboratory exposure in the second B. melitensis case. Based on the retrospective analysis of laboratory data, we estimated the resulting additional workload of implementation of the biosafety pop-up to be less than one blood culture bottle per week on average to be processed in a Class 2 biological safety cabinet.
Conclusion
Our experience demonstrates that implementation of the biosafety software pop-up can reduce the risk of laboratory exposure to Brucella spp. This intervention provides a feasible approach even in a setting where Brucella spp. are normally only encountered every few years.
期刊介绍:
The journal Microbial Risk Analysis accepts articles dealing with the study of risk analysis applied to microbial hazards. Manuscripts should at least cover any of the components of risk assessment (risk characterization, exposure assessment, etc.), risk management and/or risk communication in any microbiology field (clinical, environmental, food, veterinary, etc.). This journal also accepts article dealing with predictive microbiology, quantitative microbial ecology, mathematical modeling, risk studies applied to microbial ecology, quantitative microbiology for epidemiological studies, statistical methods applied to microbiology, and laws and regulatory policies aimed at lessening the risk of microbial hazards. Work focusing on risk studies of viruses, parasites, microbial toxins, antimicrobial resistant organisms, genetically modified organisms (GMOs), and recombinant DNA products are also acceptable.