Clinical Endoscopy

The Korean Society of Gastrointestinal Endoscopy (대한소화기내시경학회)
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Infectious transmission from Savary dilators is uncommon: retrospective review from a large tertiary academic center

  • Received : 2021.01.18
  • Accepted : 2021.03.21
  • Published : 2022.09.30
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Abstract

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References

  1. Wendorf KA, Kay M, Baliga C, et al. Endoscopic retrograde cholangiopancreatography-associated AmpC Escherichia coli outbreak. Infect Control Hosp Epidemiol 2015;36:634-642. https://doi.org/10.1017/ice.2015.66
  2. Kenters N, Huijskens EGW, Meier C, et al. Infectious diseases linked to cross-contamination of flexible endoscopes. Endosc Int Open 2015;3:E259-E265. https://doi.org/10.1055/s-0034-1392099
  3. Rutala WA, Weber DJ; the Healthcare Infection Control Practices Advisory Committee (HICPAC). Guideline for disinfection and sterilization in healthcare facilities, 2008 [Internet]. Atlanta (GA): Centers for Disease Control and Prevention; 2008 [updated 2019 May 24; cited 2021 Apr 6]. Available from: https://www.cdc.gov/infectioncontrol/guidelines/disinfection/index.html.
  4. Alfa MJ, Sepehri S, Olson N, et al. Establishing a clinically relevant bioburden benchmark: a quality indicator for adequate reprocessing and storage of flexible gastrointestinal endoscopes. Am J Infect Control 2012;40:233-236. https://doi.org/10.1016/j.ajic.2011.02.023
  5. Bisset L, Cossart YE, Selby W, et al. A prospective study of the efficacy of routine decontamination for gastrointestinal endoscopes and the risk factors for failure. Am J Infect Control 2006;34:274-280. https://doi.org/10.1016/j.ajic.2005.08.007
  6. Centers for Disease Control and Prevention (CDC). A rational approach to disinfection and sterilization [Internet]. Atlanta (GA): CDC; 2016 [updated 2016 Sep 18; cited 2021 Apr 6]. Available from: https://www.cdc.gov/infectioncontrol/guidelines/disinfection/rational-approach.html.
  7. US Food and Drug Administration (FDA). Reprocessing medical devices in health care settings: validation methods and labeling [Internet]. Silver Spring (MD): FDA; 2015 [updated 2018 Mar 6; cited 2021 Apr 6]. Available from: https://www.fda.gov/regulatory-information/search-fda-guidance-documents/reprocessing-medical-devices-health-care-settings-validation-methods-and-labeling/.
  8. Beilenhoff U, Neumann CS, Rey JF, et al. ESGE-ESGENA guideline for quality assurance in reprocessing: microbiological surveillance testing in endoscopy. Endoscopy 2007;39:175-181. https://doi.org/10.1055/s-2006-945181
  9. Reprocessing Guideline Task Force, Petersen BT, Cohen J, et al. Multisociety guideline on reprocessing flexible GI endoscopes: 2016 update. Gastrointest Endosc 2017;85:282-294. https://doi.org/10.1016/j.gie.2016.10.002
  10. The Association for the Advancement of Medical Instrumentation (AMMI). Standards Spotlight: AAMI TIR99 to provide much-needed guidance for reprocessing dilators and probes [Internet]. Arlington (VA): AMMI; 2018 [updated 2018 Oct 1; cited 2021 Apr 6]. Available from: https://www.aami.org/news/article/StandardsSpotlight-AAMI-TIR99-to-Provide-Much-Needed-Guidance-for-Reprocessing-Dilators-and-Probes-71335.