1 The Short Story on Long Cycles Why the length of your steam sterilization cycle may effect your sterility assurance.

Slides:



Advertisements
Similar presentations
Pest Risk Analysis (PRA) Training
Advertisements

Basic Principles of GMP
MSc Dissertation Writing
1 Drafting a Standard n Establish the requirements n Agree the process n Draft the Standard n Test the Standard n Implement the Standard.
AS9102 First Article Inspection Report
Biopharmaceutical Quality
Validating Sterilization of Medical Devices
1 Procuring a Design Project engineers perspective on starting the design process and establishing the A/E scope of work Frank C. Quigley General Engineer.
Dr Casey Wilson, 2009 Panels and Reviews. 1 st year Panels Dr C. Wilson, 2009 Format: (check details with your Dept) Chair, supervisor(s) and at least.
CESO Education Day November 30, 2004 Shawn Kenny Manager, Central Processing Department University Health Network – Toronto General Hospital.
Irradiator Specification Installation Qualification (IQ) + Software validation Operational Qualification (OQ) Performance Qualification (PQ) Demonstrate.
Variation in Sterilization Cycles: The continued need for load monitoring devices.
VALIDATION – ARE WE DOING ENOUGH David McNamara Manager – CSSD Holy Spirit Northside Private Hospital SRACA (NSW) Conference 10 th November 2011.
SAFE-ITSM STANDARDS.
Chemical Indicators: Class 5 Integrating Indicators
Large Taper Files. Engine-driven files Hand-Using Large Taper Files.
Cleaning, Packaging & Sterilization of Surgical Instruments
STEAM Sterilization Issues (Extended Cycles & Flashing)
1 MANUFACTURING AND PRODUCTION OF BIOLOGICAL PRODUCTS (ERT 455) HAZARD ANALYSIS AND CRITICAL CONTROL POINT (HACCP) SYSTEM Munira Mohamed Nazari School.
ETHYLENE OXIDE STERILIZATION VALIDATION
Disinfection and Sterilization of Patient-Care Equipment
MEDICAL DEVICE STERILIZATION
Sterilized, Validated, Documented and Pyrogen Tested Wipers
Good hygienic practices
Autoclave Validation Presented by Paul Yeatman BSc. Microbiologist.
Huzairy Hassan School of Bioprocess Engineering UniMAP.
HACCP Training Guide
STERILIZATION HEALTHCARE Steam Sterilizers Operation and Preventative Maintenance.
CLINICAL ENGINEERING part(3) Dr. Dalia H. Elkamchouchi.
Cleaning, Packaging & Sterilization of Dental Instruments
Disinfection and Sterilisation Practical Aspects.
8.02 Aseptic Techniques Implement aseptic technique to maintain equipment Images courtesy of google images.
FLASHTITE INSTRUCTIONS FOR USE Copyright 2010 © Case Medical Inc.
Monitoring the Sterilization Process
Part F Blood and fluid exposure Exposure? Injury with sharp object. Contamination of open wound with blood or body fluid. Eye or mucosal splash with.
9 - 2 Hazard Analysis Critical Control Point 9 - The HACCP Philosophy 3 Prevented Eliminated Reduced to safe levels If significant biological, chemical,
Leukocyte-Reduced Blood Components Lore Fields MT(ASCP)SBB Consumer Safety Officer, DBA, OBRR, CBER September 16, 2009.
CENTRAL STERILE PROCESSING
Errors & Power. 2 Results of Significant Test 1. P-value < alpha 2. P-value > alpha Reject H o & conclude H a in context Fail to reject H o & cannot conclude.
Play Instructions: 1) Divide into Teams 2) Ask a Question to a Team 3) If correct, click the Spin Wheel Button to choose the number of points that team.
ST220 Concorde Career College. Objectives List the three phases of the instrument cycle, identify the tasks performed during each phase, and describe.
© Institute for International Research, Inc All rights reserved. Module 6: Manufacturing Throughput.
Network design Topic 6 Testing and documentation.
WFHSS 2015 Lille/France Klaus Roth SMP GmbH Prüfen Validieren Forschen Hechingerstrasse Tuebingen Germany Validation of hydrogene peroxide Sterilizers.
Chemical Sterilization
Biological indicators role in CSSD equipment qualification and monitoring Paulo Roberto Laranjeira 1.
STRILIZATION AND DISINFECTION IN A DENTAL CLINIC
Felicia Krizman BSN, CRCST  Infection control/ Patient Safety specialist/ Central supply supervisor.
Wet Packs: Strategies for Prevention and Resolution
 * Sterilization: Complete destruction of all transmission m.o (bacteria,virus) * Disinfection: remove only organisms that cause disease.
NANCY CHOBIN, RN, AAS, ACSP, CSPM, CFER CHOBIN & ASSOCIATES CONSULTING HOT TOPICS IN STERILIZATION AND DISINFECTION.
SteriTite Instructions for use
Warm-Up In your journal, write a minimum, 5 sentence paragraph that describes what you just watched in the video.
Quality control and Innovation in cleaning and sterilisation indicators Denys Dhiver Albert BROWNE Ltd.
HOLD-TIME STUDIES.
World Health Organization
Sterilization Types & Control
به نام خدایی که در این نزدیکی است
Author: Nurul Azyyati Sabri
Lesson 5: BRITE Seminar: GMP II
Presented by: Healthmark Industries
Cleaning Verification
Sterilization process
Progress Test 4 Review Part B.
What is a Material Safety Data Sheet (MSDS)?
How to Conduct a Sterilization Failure Investigation
Sterilization September 2018.
יוסי שדמתי רק איכות מניהול סיכונים לאימות ותיקוף תהליכי הרכבה From Risk Management to Processes Validation יוסי.
Current Practice Re-Usable Sharps Why are hospitals making this change? How does it work? Program Benefits Next Steps.
PRODUCT FAMILY – Another Perspective
Presentation transcript:

1 The Short Story on Long Cycles Why the length of your steam sterilization cycle may effect your sterility assurance

2 A Canadian Standard Cycle? CSA does not recognize a standard steam cycle length Most common pre-vacuum cycle in Canada is a 4 minute exposure at o C Scientific evidence that 2 minutes of exposure kills highly resistant bacterial spores (Geobacillus stearothermophillus)

3 Who Determines Cycle Length? CSA-Z (Sterilization of medical devices) states: This standard specifies requirements for the information to be provided by the medical device manufacturer, so that the medical device can be processed safely and will continue to meet its performance specification. Requirements are specified for processing that consists of all or some of the following activities: –preparation at the point of use; –preparation, cleaning, disinfection; –drying; –inspection, maintenance and testing; –packaging; –sterilization; –storage.

4 Why Longer Cycles? Increased weight, density and complexity of instrument trays (particularly for orthopedic instrument sets) European validation studies at cycles that are not typical in North America (i.e. 8 min, 10 min, 12 min, 15 min, 18 min or longer!)

5 What is the Problem? Extended cycles lead to decreased throughput in the department (partial loads and longer flow times) Frequent changing of sterilizer cycles may lead to errors More information required for the processing staff to remember CSA Standards require chemical and biological monitoring of steam sterilizer cycles, but current monitoring devices are intended for use in 4 minute cycles

6 Performance Validation If the monitoring devices fails to function normally in extended cycles, the results cannot be trusted Potential for false positives and false negatives Will your chemical indicators delaminate? Is the growth media in your BI able to support normal growth after exposure to an extended cycle? Has the manufacturer validated this information?

7 What is Being Done? AAMI/CSA are considering establishment of 2-3 standard cycle lengths (i.e. 4 min, 10 min, and 20 min) Medical device manufactures re-validating their products for 4 minute cycles Hospitals are breaking down heavy and complex sets to allow sterilization in 4 minutes (with manufacturer validation)

8 What Shouldnt be Done Run 4 minute cycles for devices requiring longer cycles and assume (hope!) that sterilization has occurred Attempt in-house validation of sterility at 4 minutes - hospitals do not have the facilities to make this confirmation

9 Recommended Steps 1.Standardize to two or fewer extended cycles (i.e. 10 min and 20 min) and require device manufactures to validate to them. 2.Dedicate one sterilizer to be used for extended cycles, reducing the chance of an error 3.Specify a performance validated test pack for monitoring sterilizer loads with extended cycle Confirm the validation has been completed by independent laboratories and follows industry-accepted protocol 4.Require performance validated Class 5 chemical indicators to be placed in the trays in the most challenging locations

10 Stay Informed! Attend industry association meetings and education seminars Read relevant journal articles Ask questions of your vendors and require documentation Dont accept the status quo!