Autor: |
George Samson, Thomas Carrigan, Kevin J. Weatherwax, Charles Newman, Archie C Brown, Denis Foo Kune, Balasundaram Lavan, Kim A. Eagle, Nathan Sovitch, Ed Goldman, Hakan Oral, Daniel Alyesh, Thomas Crawford, Sandra Lach Arlinghaus, Craig Allmendinger, Andrew B. Hughey, Timir S. Baman, Sheldon Davis, Karman Tandon, Jay Snell, Pat Sovitch, Daniel Lautenbach, Noah Klugman, Brad Wasserman |
Rok vydání: |
2017 |
Předmět: |
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Zdroj: |
JACC: Clinical Electrophysiology. 3:623-631 |
ISSN: |
2405-500X |
DOI: |
10.1016/j.jacep.2016.12.007 |
Popis: |
Objectives This study sought to develop a validated, reproducible sterilization protocol, which could be used in the reprocessing of cardiac implantable electronic devices (CIEDs). Background Access to cardiac CIED therapy in high-income and in low- and middle-income countries varies greatly. CIED reuse may reduce this disparity. Methods A cleaning and sterilization protocol was developed that includes washing CIEDs in an enzymatic detergent, screw cap and set screw replacement, brushing, inspection, and sterilization in ethylene oxide. Validation testing was performed to assure compliance with accepted standards. Results With cleaning, the total mean bioburden for each of 3 batches of 10 randomly chosen devices was reduced from 754 to 10.1 colony-forming units. After sterilization with ethylene oxide, with 3 half-cycle and 3 full-cycle processes, none of the 90 biological indicator testers exhibited growth after 7 days. Through cleaning and sterilization, protein and hemoglobin concentrations were reduced from 99.2 to 1.42 μg/cm 2 and from 21.4 to 1.03 μg/cm 2 , respectively. Mean total organic carbon residual was 1.44 parts per million (range 0.36 to 2.9 parts per million). Endotoxin concentration was not detectable at the threshold of Conclusions CIEDs can be cleaned and sterilized according to a standardized protocol achieving a 12-log reduction of inoculated product, resulting in sterility assurance level of 10 –6 . |
Databáze: |
OpenAIRE |
Externí odkaz: |
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