المملكة العربية السعودية وزارة الصحة اإلدارة العامة لمكافحة عدوى المنشئات الصحية

Similar documents
THE BASICS OF DECONTAMINATION

STERITITE INSTRUCTIONS FOR USE

Christina Bradley Laboratory Manager Hospital Infection Research Laboratory Queen Elizabeth Hospital Birmingham, UK

DRAFT. Module 4. Decontamination & Environmental Cleaning

When you sterilize an instrument set, you know what the standards are.

CLEANING INSTRUCTIONS

PERFORM Operating Document

Best Practice Guidelines For Cleaning, Disinfection and Sterilization of Critical and Semi-critical Medical Devices

CLEANING AND HANDLING OF WRIGHT INSTRUMENTS

2015 Myco Industries, Inc Fax:

INSTRUCTIONS FOR CLEANING AND STERILIZATION OF ALL B.BRAUN AESCULAP HAND HELD SURGICAL INSTRUMENTS AND POWER PRODUCTS (UNITED KINGDOM REQUIREMENTS)

Accessories. Maybachstraße. Symmetry Fax: Revised 10/15

SKLAR COATED SURGICAL INSTRUMENTS RECOMMENDED CARE & CLEANING INSTRUCTIONS

SterilContainer S for use in the Steris V-PRO 60 Low Temperature Sterilization System

Cleaning & Sterilization

Instructions for Use Spinal Punches IFU

Fiona Collins Liliana Donatelli Andrew Smith

AMSCO STERILIZATION CONTAINER SYSTEM User s Guide

I.F.U Re/Processing Reusable Medical Devices

Operating / User Manual

PICNet CONFERENCE 2013

ULTRASONIC (SONIC) CLEANING ENHANCES THE INSTRUMENT

INSTRUCTIONS FOR CLEANING AND STERILISING HUMECA MEDICAL EQUIPMENT FOR BOTH ELECTRIC AND MANUAL DEVICES

CLEANING OF INSTRUMENTS

The Do's and Don ts in the Instrument Sterilisation Process

Cleaning and Sterilization for Instruments & Posts

HOMES AND SENIORS SERVICES. APPROVAL DATE: April 2004 REVISION DATE: March 2016 REVISION DATE: March 2017 REVIEW DATE: November 2018

Central Sterile Services Department will receive, decontaminate, process, store and/or dispense sterile and non-sterile to departments requesting.

SUBJECT: Monitoring the performance of a sonic cleaners and/or automatic washers cleaning ability for lumens/cannulated items daily.

CONVENTUS CAGE TM - DR Procedure Instruments Instrument Tray. Equipment Cleaning and Sterilization

Instructions for care, maintenance, cleaning and sterilization of Smith & Nephew orthopaedic devices

CONVENTUS CAGE TM PH Procedure Instruments Instrument Tray Cleaning and Sterilization

Housekeeping and Laundry Ulrika Ransjö

The Principles, The Process, and The Results:

Cleaning and Sterilisation for Burs, accessories and filling material

Processing instructions for the Ligamys suture forceps

MARSHALLTOWN MEDICAL AND SURGICAL CENTER LAUNDRY/LINEN SERVICES. SUBJECT: Infection Control POLICY NO: 106

Principles and Techniques of Instrument Processing and Sterilization

AS Medizintechnik GmbH Sattlerstrasse 15, Tuttlingen, Germany Tel 07461/ Fax 07461/

Commit 2 Clean TM/MC. Bloodborne Pathogens Awareness Program

CONVENTUS CAGE TM PH Procedure Instruments Instrument Tray Cleaning and Sterilization

Manual Pre-disinfection/Cleaning and Sterilization Instructions for SATELEC Tips and Files

CLEANING FOR EXTENDED TOOL LIFE & IMPROVED TABLET QUALITY. natoli.com

PROFESSIONAL USER GUIDELINES FOR PRACTICE INFECTION CONTROL AND HYGIENE IN VETERINARY EQUINE PRACTICE

Rigid Reusable & Single use Sigmoidoscopes, Anoscopes, and Accessories ENGLISH 1. Perform reprocessing immediately after each use.

Manual Pre-disinfection/Cleaning and Sterilization Instructions for SATELEC Tips and Files

FLASH PAK STERILIZATION CONTAINER SYSTEM

THE ULTRASONIC DISRUPTION OF ORGANIC SOIL ON COMPLEX INSTRUMENTATION

SUGGESTED POLICY FOR THE MONITORING AN ULTRASONIC CLEANER DAILY

CODE OF PRACTICE. No 11 CLEANING OF EQUIPMENT AND PREMISES

EZ9Plus & EZ11Plus Instructions on: Operating

PROFESSIONAL USER GUIDELINES FOR PRACTICE INFECTION CONTROL AND HYGIENE IN VETERINARY EQUINE PRACTICE

User Guide for Reprocessing of the SUPER VIEW Wide Angle Viewing System Sterilizable Components and Accessories

EMERGENCY RESPONSE GUIDE IMMEDIATE EMERGENCY PROCEDURES

Purpose. Team Roles and Responsibilities. System Requirements. Instrument Processing Training

Wet Loads presentation Tim Galekop Abstract 2006

Steam Sterilization and Sterility Assurance in Health Care Facilities ANSI/AAMI ST79. Suzanne Latta, CSPDT. Education Materials Coordinator

4/8/2014 GOAL PATIENT EQUIPMENT

CLEANING FOR INFECTION CONTROL Ultrasonic Cleaners. Ultrasonic Cleaners. Copyright Quality Medical Innovations P/L & Majac Medical Products P/L

Made in USA. Sunoptic Technologies 6018 Bowdendale Avenue Jacksonville, FL 32216, USA (904)

Dianne Harrison, Supervisor QA Lab

AS Medizintechnik GmbH Sattlerstrasse 15, Tuttlingen, Germany Tel 07461/ Fax 07461/

Ultrasonic From delicate microsurgery instruments to heavy duty sets

Rapid Heat Sterilizers with 6, 8, and 12 Minute Sterilization Cycle Times

GETINGE CLEAN DETERGENT RANGE GET MAXIMUM PERFORMANCE VALIDATED

Manual Pre-disinfection/Cleaning and Sterilization Instructions for SATELEC wrenches

The Hydrim C51wd Washer Disinfector. Perfectly prepares instruments for sterilisation in as little as 19 minutes.

RECOMMENDATIONS FOR CLEANING DEVICES

WORLD LEADERS IN ADVANCED SURGICAL INSTRUMENT REPROCESSING TECHNOLOGY

Effective Date: 0 8 / 1 0 / 1 7. Replaces: 08/11/16. Formulated:1997 SPECIAL (MEDICAL) WASTE MANAGEMENT

CLEANING AND SANITATION Policy Owner: Erica Tennessen Policy Originated by (program or department): Program Applicable Programs: All Programs

Reprocessing Reusable Medical and Dental Equipment: Policy and Protocols First Nations and Inuit Health Alberta Region

Infection Control Manual Residential Care Part 3 Infection Control Standard IC9: Environmental

Operator s Manual. Video Laryngoscope. ( Instructions for use ) Doc no: Revision 1.1 8th January 2013

Cleaning and disinfecting

Veterinary Autoclave

Recommendations for cleaning, decontamination and sterilisation. devices

Manual Cleaning? SOBECC Round Table: Manual and Automated Cleaning Methods th July 2012

RAP-hip Hip stem extraction set

Corporate. Laundry SOP. Document Control Summary

WORK IN THE DISINFECTION ROOM WITH WASHER-DISINFECTORS

Jennings Street School

Safe Use of a Class II Biological Safety Cabinet

INSTRUCTIONS EVIS EXERA II DUODENOVIDEOSCOPE

Accurately With HSE COP PT 1 5

Institute of Decontamination Sciences Blackburn House, Redhouse Road, Seafield, Bathgate, West Lothian EH47 7AQ


Harvey Chemiclave 5000 Owner And Operator Guide

AS Medizintechnik GmbH Sattlerstrasse 15, Tuttlingen, Germany Tel 07461/ Fax 07461/

STERILIZATION IS A KEY RESPONSIBILITY OF THE INSTRUMENT

Aesculap Implant Systems

Operating Manual "Mark II" Solid-State Digital Automatic Controlled Sterilizers

Integra Salto Talaris and Integra XT Non-Sterile Device Reprocessing. Instructions for Use. 4. Manual Cleaning Instructions

EMAX 2 PLUS AND XMAX CLEANING AND STERILIZATION BASKET. Mechanical/Automated Cleaning and Sterilization Guide in a Variety of Applications

Cleaning and Sanitation Procedures Module Deli

HTM made easy. Testing Explained... in fact everything you need to know about HTM but were too afraid to ask!

PROFESSIONAL USER GUIDELINES FOR PRACTICE INFECTION CONTROL AND HYGIENE IN COMPANION ANIMAL VETERINARY CLINICS/HOSPITALS

DEVICES THAT HAVE NOT BEEN ADEQUATELY CLEANED CANNOT

HYGIENE AND SANITATION

Transcription:

1. POLICY STATEMENT: Cleaning, decontamination and sterilization method should be done in CSSD service facility not in the end user department side. 2. PURPOSE: To ensure the proper way of collections, decontamination, cleaning and Sterilization of all instruments in CSSD. 3. SCOPE: This policy is applied to all CSSD personnel. 4. DEFINITIONS: 4.1 Cleaning: is the removal of all foreign material (dirt and organic matter) from The object being reprocessed? 4.2 Decontamination: the physical or chemical methods to remove inactive, or destroy microorganisms, rendering them safe for handling. 4.3 Sterilization: is a process which all viable forms of microorganisms (including Spores) are destroyed. 5. RESPONSIBILITIES: The following functions are performed the CSSD Staff. 6. PROCEDURES 6.1 Cleaning 6.1. 1.Two key components of cleaning are friction to remove foreign matter and fluids to remove or rinse away contamination. 6.1. 2.Thorough cleaning will remove most organisms from a surface and should always precede disinfection and sterilization procedures 6.1.3. If instruments and other items have not been cleaned, sterilization and disinfection may not be effective because microorganisms trapped in organic material may survive after sterilization or disinfection 6. 1.4.Cleaning is normally accomplished the use of water, detergents and mechanical actions via many types of brushes (do select the suitable one ) 6. 1.5. Detergent is essential to dissolve proteins and oil that can reside on instruments and equipment after use. 6.1.6. All personnel who clean or reprocess equipment should use appropriate protective Page 1 of 5

barriers for the procedure being performed (i.e. gowns, gloves, goggles, masks, etc). This may vary according to the cleaning disinfectant agent or the item being reprocessed. 6.2. Mechanical Cleaning Mechanical cleaning facilitates cleaning and decontamination of some items. 6.2.1.Washing disinfectors (Common Criteria ) The washing machine gives a cold rinse followed a hot wash at 71 C for 2 minutes. This is followed a 10-second hot water rinse at 80-90 C and then drying a heater or a fan at 50-75 C. See ST-07. 6.2.2. Ultrasonic cleaner Ultrasonic cleaning removes soil a process called cavitation in which waves of acoustic energy are propagated to disrupt bonds that hold particular matter to surfaces, see ST-08. 6.3. Manual Cleaning 6.4.1. All items requiring disinfection or sterilization should be dismantled before cleaning. Warm water is preferred; it will remove most of the protein materials (blood, sputum, etc.) that would be coagulated heat and would subsequently be difficult to remove. The most simple, cost-effective method is to thoroughly brush the item while keeping the brush below the surface of the water in order to prevent the release of aerosols. 6.4.2. The brush shall be decontaminated after use and shall be dried. Finally, items shall be rinsed in clean water and then should be dried. Items are then ready for use (non-critical items) or for disinfection (semi-critical items) or for sterilization (critical items). 6.4.3 Manual cleaning is necessary when: 6.4.3.1. Mechanical cleaning facilities are not working. 6.4.3.2.Delicate instruments have to be cleaned; 6.4.3.3.Complex instruments need to be taken apart to be cleaned; 6.4.3.4. Items with narrow lumens need to be cleaned (endoscopes). 6.5 Manual or hand-cleaning must be done with extreme caution 6.5.1 Wear heavy-duty rubber gloves, a plastic apron, eye protection, and mask during cleaning. 6.5.2 Soak the instruments in normal tab water containing a detergent. Page 2 of 5

6.5.3 Scrub instruments and other items vigorously to completely remove all foreign material using a soft brush or special brush, detergent, and water. Hold items under the surface of the water while scrubbing and cleaning to avoid splashing. Disassemble instruments and other items with multiple parts, and be sure to brush in the grooves, teeth, and joints to items where organic material can collect and stick. 6.5. 4. Flush through lumens with an adapted water jet. 6.5.5. Rinse items thoroughly with clean water to remove all detergent. Any detergent left on the items can reduce the effectiveness of further processing 6.5.6. Inspect items to confirm that they are clean. 6.5.7..Allow items to air dry or dry them with dryer or a clean towel (in case of dryer M/C not available) if chemical disinfection is going to be used. This is to avoid diluting the chemical solutions used after cleaning. Items that will be high- Level disinfected then will be treated boiling or steaming does not need to be dried. 6.6 Recommendations for Packaging Supplies to be Sterilized 6.6.1They must withstand the physical conditions of the sterilization process chosen for the device. 6.6.2. They must allow for adequate air removal. 6.6.3. They must be easily penetrated the saturated steam. 6.6.4. It must be possible to seal them in such a way that tampering will be evident. 6.6.5. It must be adapted to the size and shape of the item to be packed. 6.6.6. They must resist tearing and puncturing under ordinary conditions of use. 6.6.7. They must protect the package contents from physical damage. Page 3 of 5

6.6.8. They must allow aseptic removal of the contents. 6.6.9. External chemical indicators should be placed on the outside of the packaging material. They may be used as a form of closure for the package such as indicator tape. Use the Bowie/Deck test and the Biological Indicator as per the manufacturer recommendation and ISO 11138 and ISO 11140 standards. 6.6.10. The appropriate internal chemical indicator should be placed in the center of the package in the center of the tray. If the internal chemical indicator does not indicate that the item has been sterilized, it should be reported with the load control number to the Manager/Director of the Sterile Processing Department and the item(s) should be reprocessed and sterilized before use. 6.7 Sterilization Steps for steam sterilization as following :-. 6.7.1 Arrange all labeled packs, containers, or unwrapped items in the chamber of the autoclave in a way that allows the steam to circulate freely. 6.7.2 Follow the manufacturer instruction for operating the autoclave. Adjust time, temperature and pressure according to the table. 6.7.3 If the autoclave is automatic, the heat will shut off and the pressure will begin to fall off once the sterilization cycle is complete 6.7.4 If the autoclave is not automatic, turn off the autoclave after achieving the required time. 6.7.5 Wait until the pressure gauge reads 0 to open the autoclave. Open the lid or door to allow remaining steam to escape. Leave all items in the autoclave until they dry completely. It may take up to 30 minutes. 6.7.6 Remove packs, containers, or unwrapped items from the autoclave using sterile pick-ups to handle unwrapped items. The packs of equipment should come out of the autoclave dry. Wet packs must be considered non-sterile. Do not store packs, containers or wrapped items until they cool to room temperature. Page 4 of 5

7. REVISION AND AUDIT: This Policy will be reviewed every two years or when necessary. 8. REFERENCES: Association for the Advancement of Medical Instrumentation Advanced AAMI 2011, The International Association of Healthcare Central Service Materiel Management IAHCSMM 7 th Edition, CDC Disinfection and sterilization Guide lines 2009, APIC Guidelines 2009 Chapter 55. Policy Number ST-06 Prepared Reviewed Approved Approval Date : Revision Date : Page 5 of 5