Sterilization – In General What’s the process? –Decontamination – removes > 80% of microbes –Sterilization – Kills/inactivates the remaining microbes What.

Slides:



Advertisements
Similar presentations
Basic Refrigeration, Its Components, and Its Cycle
Advertisements

Culturing Microbes.
Validating Sterilization of Medical Devices
1 The Short Story on Long Cycles Why the length of your steam sterilization cycle may effect your sterility assurance.
CESO Education Day November 30, 2004 Shawn Kenny Manager, Central Processing Department University Health Network – Toronto General Hospital.
Chemical Indicators: Class 5 Integrating Indicators
Kinetics Class #4 OB: reactions that are in dynamic equilibrium and how to “push” them forward, or reverse using LeChatelier's Principle.
ETHYLENE OXIDE STERILIZATION VALIDATION
Disinfection and Sterilization
Clean? Disinfect? Sterilize? What does it all mean??
MEDICAL DEVICE STERILIZATION
DENT 1260 IC Unit 5 Unit 5 Sterilization 1. 3 methods of HEAT Sterilization Autoclave- steam under pressure Chemclave- chemical heated under pressure.
Autoclave Use and Safety
STERILIZATION HEALTHCARE Steam Sterilizers Operation and Preventative Maintenance.
Gas Turbine Power Plant
Good Hygiene Practices Managing Hygiene through Temperature Control Sub-Module 5.3, Section 2.
Cleaning, Packaging & Sterilization of Dental Instruments
Sterilization Methods
Disinfection and Sterilization.
Physical and Chemical Control of Microorganisms
Autoclave. What is an Autoclave? Autoclave is a pressurized device designed to heat aqueous solutions above their boiling point at normal atmospheric.
Monitoring the Sterilization Process
Specific heat and phase changes
Lab 5: Atmospheric Moisture.
Physical and Chemical Control of Microorganisms. Control of Microorganisms by Physical and Chemical Agents.
CHEMISTRY 2000 Topic #3: Thermochemistry and Electrochemistry – What Makes Reactions Go? Spring 2012 Dr. Susan Lait.
INTRODUCTION TO FREEZE-DRYING.
Sterilizers.  Definition of sterile  Free of microorganisms (bacteria) Bacteria  Bacteria can be broken down into two groups  Pathogenic - cause disease.
Sterilization of Medical Devices: Bodhisatwa Das.
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.
A Basic Introduction & Some Cool Stuff
Reaction Rates Chapter 17 Honors Chemistry Red  Blue Reaction Rates.
WFHSS 2015 Lille/France Klaus Roth SMP GmbH Prüfen Validieren Forschen Hechingerstrasse Tuebingen Germany Validation of hydrogene peroxide Sterilizers.
Power Plant Engineering
Sterilization and Disinfections. Sterilization Freeing of an environment from all living microorganisms includes bacteria and their spores, fungi, parasites.
The Control of Microbial Growth
Chemical Sterilization
Infection Control and Medical Asepsis
STRILIZATION AND DISINFECTION IN A DENTAL CLINIC
Water in the Atmosphere Chapter 18, Section 1. Water in the Atmosphere  Precipitation – any form of water that falls from a cloud  When it comes to.
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.
Sterilization Lab 3 Abeer Saati.
Describing Reaction Rates Kinetics How fast does the reaction go? Reaction Rate : the change in the amount of reactant or product per unit time.
1 Chapter 1 Chemistry: The Study of Matter. 2 What is Chemistry?  The study of the matter, its composition, properties, and the changes it undergoes.
Chemical Kinetics. The branch of Physical chemistry which deals with the rate of reactions is called chemical kinetics. The study of chemical kinetics.
Agricultural microbiology course
Biotechnology 2.  The method of choice for sterilization in most labs is autoclaving; using pressurized steam to heat the material to be sterilized.
Laboratory equipment Lecture (5).
Sterilization Types & Control
به نام خدایی که در این نزدیکی است
Natural Gas Production Chapter 5 Dehydration of Natural Gas
Processing Food by Heat
Practical Medical Bacteriology
NYC APIC Monthly Meeting Questions and Answers
Sterilization process
Progress Test 4 Review Part B.
How to Conduct a Sterilization Failure Investigation
Sterilization September 2018.
CS Cheat Sheet.
Welcome To study the principle and application of important instrument used in the microbiology laboratory.
Sterilization and disinfection
Dental Assisting DNT 354 (Sterilization)
Antimicrobial Agents and Immunology
 Define: The stirring heating plate or heated stirring heating plate has been developed to heat and mix fluids contained in laboratory receptacles such.
Presentation transcript:

Sterilization – In General What’s the process? –Decontamination – removes > 80% of microbes –Sterilization – Kills/inactivates the remaining microbes What are the Sterilants? –Saturated Steam –Ethylene Oxide –Ozone –Hydrogen Peroxide –High Level Disinfectants (Glutaraldehyde, OPA, PAA)

Sterilization – In General What’s the process? –Decontamination – removes > 80% of microbes –Sterilization – Kills/inactivates the remaining microbes What are the Sterilants? –Saturated Steam –Ethylene Oxide –Ozone –Hydrogen Peroxide –High Level Disinfectants (Glutaraldehyde, OPA, PAA)

Steam Sterilization “Critical” Variables –Time. –Temperature. –Saturated Steam. (Depends on Temperature and Pressure) Other Variables (Incomplete List) –Loading –Sterilant contact with items to be sterilized –Outside weather changes –Boiler Chemicals –Wrapping Materials –Etc, etc, etc…….

Saturated Steam Wet Steam/ Liquid Water Superheated Steam

Saturated Steam – What is it? It is a colourless gas, containing < 3% liquid water Depends on temperature and pressure It will condense if it cools down a fraction of a degree It releases latent or potential heat energy as it condenses It is the latent or potential heat transferred to microbes that kills/inactivates them

Latent Heat = Potential Energy 16 Tons 16 Ton weight is sitting on the floor It has zero Potential energy Researcher knows the 16 ton weight has zero Potential energy. She is not afraid.

Latent Heat = Potential Energy 16 Tons 2 meters 16 ton weight is now 2 meters off the ground. It has quite a lot of potential energy with respect to the researcher The researcher is now very afraid of the 16 ton weight’s potential energy

Latent Heat = Potential Energy 16 Tons 2 meters Latent or Potential energy from the 16 ton weight is now realized. Especially by the late Researcher.

Latent Heat = Potential Energy 16 Tons 16 Tons Steam (Gas) Water (Liquid)

The “Experiment” Generating Saturated Steam at 1 Atmosphere Temp Time 100ºC All the energy is now going in To creating “latent” heat in the steam With no increase in temperature It takes 150 KJoules to heat 1 lb of water from 20ºC to 100ºC and 1023 Kjoules to convert 1 lb of water from liquid to gas at 100ºC

Typical Steam Sterilizer

Sterilization Monitoring We monitor the Process not sterility of items Because the process is validated (by the manufacturer of the sterilizer) we assume that, if the process functions correctly, the goods in the process will be sterile.

Process Monitors for Steam Sterilization 3 Major types used: Biological Indicators: –Monitor all variables in the process Chemical Indicators: –Monitor one or more of the critical variables Mechanical Indicators: –Monitor one of the critical variables

Process Monitors for Steam Sterilization Individually they provide information, but only together do they tell the whole story! A failure in any one of the monitors implies the process is incomplete in one or more necessary variables

Biological Indicators Large # (> 10 5 or 10 6 ) of resistant spores Usually “Self-contained” type Placed in a normally loaded sterilizer At least one per day per cycle (CSA) Final Readout made at 1, 3, 24 or 48 hours Test the process to ensure it is capable of killing microorganisms

Vial SporeStrip Ampoule + Growth media & Indicators Filter Cap Self-contained Biological Indicator

How do they Work? Colour change indication: –If spore survives, it is incubated –Spore consumes nutrients, excretes acid –Spore creates subsequent generations that also consume nutrients and excrete acids –Purple (or other) dye is acid sensitive –If enough acid is produced, dye will change from purple to yellow (or other colour change) –Process can take up to 48 hours to get reliable prediction of kill

How do they Work? Rapid Read BIs –Spore survives the sterilization cycle and is incubated –Nutrients are “tagged” with a U.V. fluorescent dye –As spore consumes nutrients the dye is released and begins to fluoresce –Fluorescence is detected electronically –Process takes up 3 hours to get reliable prediction of kill

What bout these “Extended Cycles”? G.stearothermophilus will still be the test spore. Requires a new Process Challenge Device (test pack) not a new BI Extended cycle required because bigger. Heavier more complex sets protect microbes better PCD must provide the same protection to the BI

BIs and CIs All current sterilization standards (AAMI, CSA and ISO) require the use of Biological indicators. Chemical Indicators cannot replace Biological indicators because: –Biologics are far more complex –Biologics have the potential to recover after serious damage –Chemistries only approximate the response of Biologics –Chemical kinetics are far simpler than biologic kinetics –Chemical indicators only measure the critical variables of the process. Biologics integrate all the variables of microbial death

Understanding Chemical Indicators To fully understand Chemical indicators one must understand: –BIER/CIER Vessels/Test methods used by manufacturers –Stated Values (SVs) –ISO/AAMI Classifications of Chemical Indicators –How it all relates to YOUR sterilization process –What a pass/fail result really means

Test Methods for Testing Chemical Indicators Must be reproducible, controlled and consistent Based on standard test “Sterilizers” called BIER or CIER vessels BIER = Biological Indicator Experimental Resistometer CIER = Chemical Indicator Experimental Resistometer BIER/CIER vessels performance specified by ISO BIER/CIER Vessels behave very differently from a typical health care sterilizer

BIER/CIER Vessels Very Small Chamber Very tight controls Highly reproducible results Basis for all Biological and Chemical indicator testing All CI “Stated Values” are based on this vessel

Some Requirements of CIER Vessels Come-up time < 10 seconds Come-down time < 10 seconds Vacuum air removal < 2 minutes No steam allowed during air removal Set Temperature within 0.5ºC Set Time within 1 second Pressure within 3.5 Torr One data point recorded per second

Contrast CIER Vessel to Health Care Sterilizer Come-up time 5 to 15 minutes Come-down time 5 to 15 minutes Vacuum air removal 5 to 15 minutes Steam used during air removal Set Temperature within 2ºC (?) Set Time within ?? Pressure within ?? One data point recorded per 30 seconds

Test Methods for Chemical Indicators All testing done in a CIER Vessel Must meet requirements of ISO ISO is written for Manufacturers not end users Specifications are broken in to 6 categories Only need to show the ability to reach the stated values.

Stated Values: What are they? For any given chemical indicator to be compliant with ISO , it must have “Stated Values” for the parameters it measures. Example: For a Class 3 Chemical Indicator, it must have a stated value for temperature. This is the temperature at which we can expect to see the change in the CIER vessel.

Stated Values and ISO The standard uses the “Stated Values” to define how the indicator will perform. Example: A Class 4 Indicator Stated Values: –134ºC –4 Minutes ISO allows a range: Colour change (Pass result) must be seen at 134ºC, after 4 minutes exposure in the CIER vessel. A fail (no colour change) result must be seen at 132ºC after only 3 minutes exposure. No additional testing is required at points in between.

Stated Values and ISO A Class 6 example: Stated Values: –134ºC, 4 Minutes (Saturated steam) –A pass result must be seen ( in the CIER vessel) after 4 minutes exposure at 134ºC –A Fail result must be seen at 133ºC after 3 min 45 second exposure in a CIER vessel. –No additional testing of points in between is required.

Stated Values and ISO The BIG QUESTION So, if a chemical indicator shows a “pass” result in your sterilizer does it mean that the Stated Values given for that particular chemical indicator have been achieved?

Chemical Indicators Changes (reactions that cause colour change) start at temperatures well below the stated values for the CI Temperature at which the reaction starts is the initiation temperature Changes (reactions) will continue once initiated and the temperature is above the initiation temperature

Rates of Reaction and Initiation Energies In our house my wife allows me the honour of pressing my own shirts. As part of that process I have learned a lot about the chemistry of burning fabrics.

Rates of Reaction and Initiation Energies For example, I discovered that if I place an unplugged (cool) iron on a shirt, I can leave it there indefinitely and it will not scorch the shirt. That’s because the energy imparted to the shirt from the cool iron is well below the initiation energy required to start the burning reaction of the fabric. It also doesn’t remove wrinkles

Rates of Reaction and Initiation Energies I’ve also learned that I can leave an iron on its lowest setting on the shirt indefinitely and it will not scorch the shirt either. I guess the low setting still doesn’t deliver enough energy to start the burning reaction

Rates of Reaction and Initiation Energies Of course, an iron on medium setting will scorch the shirt, but it takes quite a few minutes to do so, On high setting, the wrinkles go, but if I leave the iron on the shirt for even a short time, it will scorch.

The Scorched Shirt Example

Chemical Indicators Example (Theoretical) CI has stated values of 134ºC, 4 minutes: Initiation temperature may be 100ºC and reaction (change) will start to occur at that temperature and continue while the temperature remains over 100ºC. The rate of change will vary with temperature once initiated. Usually faster as temperature increases

BIER/CIER Vessel Testing

Same CI in a Health Care Sterilizer

Next Big Question(s) If chemical indicators start to react below the stated values: –How fast do they react at lower temperatures? –Will they change if they spend sufficient time at lower temperatures? –What does that mean for monitoring my sterilizer?

Extended Cycle Time Temperature Plot: Set Points 132ºC, 18 min)

Conclusions so far….. Stated Values cannot be duplicated in Health Care Sterilizers Stated values can be used only for comparative purposes between Chemical Indicators of the same class Stated Values are used by Manufacturers of Chemical Indicators to make CSA/ISO or AAMI Classification claims.

CSA/ISO/AAMI Classification of Chemical Indicators All follow the ISO 11140, 6 tier classification structure All state the class has no hierarchical significance. (i.e. a Class 2 is not “better” than a Class 3 or a Class 6 is not “better” than a Class 5.) Classification structure is to provide specifications and targets for manufacturers of chemical indicators It may be used by users for comparing CIs within the same class

Definitions Critical Variable –For steam sterilization Time, Temperature and Saturated Steam –For Ethylene Oxide: EtO concentration, humidity, time, temperature Critical Parameter –A set value of a critical variable that must be attained Stated Values –The critical parameters measured by a Chemical Indicator in a CIER vessel

CSA/ISO/AAMI Classification Class 1 – Process Indicators –Autoclave tapes, built-in CIs on peel pouches –Simply identify processed from unprocessed packages Class 2 – Special Indicators –Bowie-Dick Type Tests Class 3, 4, 5, and 6 are all Internal Indicators

Classes Class 3 Indicator: –Measures only one of the critical variables of the process Class 4 Indicator: –Measures 2 or more of the critical variables of the process –E.g. Time and temperature, or time saturated steam.

Classes Class 5 Integrating Indicator –Measures all critical variables of the process, and correlates with the test spore for that process across a range of sterilization conditions –For steam sterilization, the Class 5 must correlate with G.stearothermophilus at 121ºC, 128ºC* and 135ºC –Has a known response over a range of sterilization temperatures * May be other temperatures within the range of ºC

Class 5 Integrating Indicator Response

Class Class 6 Emulating Indicator –Measures all critical variables of the process –Tightest specifications of all indicators –Stated Values are for a specific time and temperature for steam sterilization

Class 6 Emulating Indicator Response

Conclusions: Saturated Steam is critical to the sterilization process Non-condensable gases (air, CO 2, N 2 ) are poor heat transfer media and poor sterilants It is the latent heat of saturated steam, not the temperature that kills the microbes

Conclusions All process monitors must agree that the cycle was successful A failure in any one of the 3 types of monitor (Biological, chemical or mechanical) means the process was insufficient and processed goods are suspect

Conclusions Biological Indicators are the only indicator to integrate all the variables of he sterilization process They are the only direct measure of the lethality of the process The BI response can be approximated by chemical indicators, but CIs cannot replace BIs

Conclusions The basis for classification of Chemical Indicators in Canada is CANISO This standard is written for manufacturers of chemical indicators. The standard has no hierarchical significance Stated values are only realizable in the test vessel (CIER vessel)

Conclusions Selection of biological indicators and chemical indicators must be made considering patient safety, the information needed from the indicators, the standard requirements, best practices and economic considerations. No single indicator will likely accommodate every circumstance