1994
DOI: 10.1086/646914
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STERIS SYSTEM 1 in Germany

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Cited by 3 publications
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“…Sterilization of a flexible endoscope may, on occasion, be possible, but the medical literature suggests it cannot be achieved reliably and consistently. [12][13][14][15][16][17][18][19][20][21][22][23][24]47 No standardized method for verifying either sterilization or disinfection in the internal channels of intact flexible endoscopes is available currently. 18 Without dismantling the endoscope to collect microbiologic samples from all of its inner surfaces, the validity of the data used to evaluate the effectiveness (or ineffectiveness) of either process may be questioned.…”
Section: Resultsmentioning
confidence: 99%
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“…Sterilization of a flexible endoscope may, on occasion, be possible, but the medical literature suggests it cannot be achieved reliably and consistently. [12][13][14][15][16][17][18][19][20][21][22][23][24]47 No standardized method for verifying either sterilization or disinfection in the internal channels of intact flexible endoscopes is available currently. 18 Without dismantling the endoscope to collect microbiologic samples from all of its inner surfaces, the validity of the data used to evaluate the effectiveness (or ineffectiveness) of either process may be questioned.…”
Section: Resultsmentioning
confidence: 99%
“…9-11 Any disinfection or sterilization process is likely to fail if the instrument is not cleaned thoroughly first. 3,[12][13][14][15][16][17] Heat and ethylene oxide gas (EtO) are the two most commonly used sterilizing agents for reprocessing medical instruments. Pressurized steam is the optimal choice for sterilization because of its reliability, availability, and cost-effectiveness.…”
Section: High-level Disinfection and Sterilizationmentioning
confidence: 99%
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