内镜洗消现状及洗消机课件.pptVIP

谢 谢！ The most common referenced document utilized in the development of policies and procedures for endoscope processing is: Standards of Infection Control in Reprocessing of Flexible Gastrointestinal Endoscopes. This is the primary document used by healthcare facilities. It covers all the requirements that should be met and goes step by step through the scope reprocessing procedure. It is very clear and easy to understand and there is an accompanying video module. A good companion to the above is the Guideline for the Use of High-Level Disinfectants and Sterilants for Reprocessing of Flexible Gastrointestinal Endoscopes. Both of these documents are written by the Society of Gastrointestinal Nurses and Associates. QUALITY ASSURANCE Each endoscopy setting should have in place an effective quality assurance program to assure adherence of endoscope reprocessing standards, availability of appropriate equipment and supplies, and procedures for reporting infections. Supervisory personnel must be familiar with current endoscope reprocessing practices to properly train and monitor staff compliance to reprocessing protocols. High-level disinfectants should be monitored daily for minimum effective concentrations daily and recorded. HLD should be changed when they fail to meet MEC or they exceed the manufacturers’ recommended use life. High-level disinfectant vapor levels should be monitored annually. A preventative maintenance plan should be in place for all AER’s and quality controls recommended by the manufacturers should be followed . PROCEDURE ROOMS Areas of the procedures rooms where scopes, accessories or specimens are handles should be designated as contaminated, and kept separate from clean areas. These areas must be cleaned with a hospital grade disinfectant between patients. Procedure rooms with negative pressure are HEPA (high efficiency particulate air) filters should be used for patients with known or suspected tuberculosis. Mayo诊所的洗消间设计被SGNA视