A Prospective, Randomized Comparison of Duodenoscope Reprocessing Surveillance Methods

Author:

De Wolfe Travis J.12ORCID,Safdar Nasia234,Meller Megan2,Marx John3,Pfau Patrick R.5,Nelsen Eric M.5ORCID,Benson Mark E.5,Soni Anurag5,Reichelderfer Mark5,Duster Megan2,Gopal Deepak V.5ORCID

Affiliation:

1. Department of Biomedical Informatics, University of Pittsburgh School of Medicine, Pittsburgh 15219, PA, USA

2. Department of Medicine, Division of Infectious Disease, University of Wisconsin—Madison, Madison 53705, WI, USA

3. Infection Control, University of Wisconsin Hospitals and Clinics, Madison 53705, WI, USA

4. William S. Middleton Memorial Veterans Hospital, Madison 53705, WI, USA

5. Division of Gastroenterology and Hepatology, Department of Medicine, University of Wisconsin School of Medicine and Public Health, Madison 53705, WI, USA

Abstract

Duodenoscope use in healthcare facilities has been associated with transmission of multidrug resistant pathogens between patients. To assist healthcare facilities in monitoring the quality of their duodenoscope reprocessing procedures and limit patient risk of infection, the Centers for Disease Control and Prevention (CDC) deployed voluntary interim duodenoscope sampling and culturing surveillance protocols in 2015. Though the interim methods were widely adopted, alternative surveillance protocols were developed and implemented at individual institutions. Here, we compared two sampling methods—the 2015 CDC interim protocol and an alternative protocol developed by the University of Wisconsin Hospitals and Clinics (UWHC). We hypothesized that the UWHC protocol would detect a higher incidence of bacterial contamination from reprocessed duodenoscopes. A total of 248 sampling events were performed at UWHC. The CDC protocol (n = 129 sampling events) required culturing samples collected from each duodenoscope after brushing its terminal end and flushing its lumen with sterile water. The UWHC protocol (n = 119 sampling events) required culturing samples collected from each duodenoscope after swabbing its elevator, immersing its terminal end into broth and flushing its lumen with saline. With the CDC method, 8.53% (n = 11) of the duodenoscopes sampled were positive for bacterial growth with 15 isolates recovered. Using the UWHC method, 15.13% (n = 18) of cultures were positive for bacterial growth with 20 isolates recovered. The relative risk of identifying a contaminated duodenoscope using the CDC interim method, however, was not different than when using the UWHC protocol. Mean processing time (27.35 and 5.11 minutes, p<0.001) and total cost per sample event ($17.87 and $15.04) were lower using the UWHC method. As the UWHC protocol provides similar detection rates as the CDC protocol, the UWHC method is useful, provided the shorter processing time and lower cost to perform.

Funder

National Institutes of Health

Publisher

Hindawi Limited

Subject

Gastroenterology,Hepatology,General Medicine

Cited by 4 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. Circular economy for medical devices: Barriers, opportunities and best practices from a design perspective;Resources, Conservation and Recycling;2024-09

2. Bacterial bioburden of duodenoscope elevator mechanism in different reprocessing stages;American Journal of Infection Control;2023-10

3. Technological review: developments in innovative duodenoscopes;Gastrointestinal Endoscopy;2022-01

4. Flexible and semi-rigid endoscope processing in health care facilities;ANSI/AAMI ST91:2021; Flexible and semi-rigid endoscope processing in health care facilities;2021-10

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