STERIS offers sterile processing accessories that help healthcare teams stay organized, maintain critical tools, and ensure protection of essential medical equipment.
One major cause that dramatically impacts patient safety is the use of unclean reusable medical equipment (RME), delivered from a sterile processing department (SPD). Unfortunately, current reprocessing practice is mostly driven by human labour and control, which is error-prone and inefficient. In ...
Sterile Processing Decontamination Sinks When medical instruments and equipment return from surgery, it's up to the Sterile Processing Department (SPD) to clean, sterilize, and prep these instruments for their next use. Without a properly equipped sterilization department, operating rooms would cease to...
This digital issue explores the challenges associated with proper cleaning and disinfection in the sterile processing department (SPD), which can be one of the most contaminated areas in the hospital, due to the nature of the work performed there -- especially in the decontamination section. ...
Service-Oriented Architecture for SPDFLOW: A Healthcare Workflow System for Sterile Processing Departments 来自 ResearchGate 喜欢 0 阅读量: 9 作者: Xiaoyu Ma,Shiyong Lu,Kai Yang 展开 摘要: Healthcare workflow has recently become an enabling technology in the healthcare industry to automate ...
A major reason is because sterile processing is truly a support department and is a non-revenue generating department. Revenue-generating departments often receive the most attention from hospital executives. Sterile processing is also still relatively unfamiliar to the public, resulting in lac...
5 closely with the department contact, understand each department professional characteristics, infection and its reasons, common hospital equipment, special requirements of products processing and opinions; 6 Master suddenly without water, power outages, equipment failure and accidentemergency measures. Profic...
Sample Processing and Protein Digestion Bradford protein assay A protein assay (Bradford assay) was performed using 10 μL of each of the 3 FFT filtrate samples; the results from this test were below the limit of detection for the assay. SDS–polyacrylamide gel electrophoresis stack gel Aliquots...
Before that time, the formal sterility-test failure investigation did not exist; rather, sterility-test positives were considered more like a minor glitch on the road to release than as a potential processing failure. Actually, my firm did take the occurrence of a sterility positive seriously, an...
Sterile is not sterile if clean is not clean." This is axiomatic in thesterile processing (SP) profession. Yet an honest appraisal of common industrypractice would conclude that the cleaning process lacks the rigorous testing,validation, verification and documentation employed in the sterilizationproces...