ANES 1501 - M8 PPT2: Asepsis and Sterile Technique
-
Upload
college-of-dupage-learning-technologies -
Category
Education
-
view
70 -
download
1
Transcript of ANES 1501 - M8 PPT2: Asepsis and Sterile Technique
HUMAN MICROBE RELATIONSHIPS
Indigenous microflora Microbes that live on the skin and inside human body “Opportunistic pathogens” Examples: bacteria, fungi, viruses, and protozoa Microflora = harmless, HOWEVER, microflora + surgical wound =
pathogen
Symbiosis Mutualism Commensalism Parasitism
PATHOGEN AND INFECTION
Pathogens Microorganisms that cause infection Commensal microbes: Opportunistic by entering through a surgical
incision Nosocomial: Urinary tract infections (UTI) Airborne viruses: Common cold
HUMAN-MICROBE RELATIONSHIPS
Mutualism: Both organisms benefit and depend on one another to a certain extent Example: Esherchia coli in the colon produces vitamin K
Synergism: Two organisms work together to achieve a result neither could obtain alone Example: Fusobacteria and spirochetes work together to cause trench mouth
Commensalism: One organism benefits but the other neither benefits nor is harmed Example: Indigenous microflora on the skin can obtain nutrients but do not
affect the skin
Parasitism: One benefits and the host is harmed Example: Intestinal worms
PATHOGENS ASSOCIATED WITH SURGICAL SITE INFECTIONS (SSI)
Bacteria Prokaryotes, binary fusion
Tuberculosis (TB) Mycobacterium tuberculosis: airborne droplet nuclei Precautions: wearing gloves, gowns, eyewear, and NIOSH-approved respirators
Viruses Non-living particles that are completely reliant on the host cell for survival Largest: 300m
Capsis: protein covering of DNA/RNA Capsomeres: the capsis is composed of protein molecules Nucleocapsid: nucleic acid-capsid combo
Smallest: 30m Poliovirus
PATHOGENS - SSI
Emerging infectious diseases Multidrug resistant strains (MDR) Strain “W” Viruses constantly mutate and evolve
Examples: ebola, dengue, Lassa
Prions Prusiner 1982 Creutzfeldt-Jakob disease (CDJ) Scrapie (“sheep disease”)
PATHOGENS – SSI
Unicellular and multicellular protozoan
Helminths: round and flat Tapeworm, flukes, and roundworms
Transmission: ingestions of contaminated food/water that contains the worm or eggs Skin, fecal-oral contamination, arthropod bite
Protozoa-unicellular eurkaryotes that are responsible for causing human diseases such as malaria and chronic sleeping sickness Amoebas, flagellates, ciliates, coccidian, and microsporidia Entamoeba histolytica: cause of amoebic dysentary
PATHOGENS – SSI: FUNGI
Mycology (study of fungi) Examples: yeast, mushrooms, and molds
Mycoses (fungal diseases) Example: Zygomycosis (bread mold) Rhinocerebral zygomycosis Increased organ transplants and immuosuppressive drugs and
antibiotics Plastic surgery and bone transplant
METHODS OF TRANSMISSION
Primary agent: bacterium, virus, fungi, or parasite
SSI: acquired at time of surgery, then after Environmental and endogenous
Personnel – WEAR PROPER ATTIRE!
Environment Fomites: inanimate objects that harbor microorganisms
Patient
FACTORS THAT INCREASE SSI
Age
Obesity
General health
Nasal carriers of S. aureus
Remote infections
Pre-op hospitalization
FACTORS AFFECTING SSI
Preexisting illness and related treatment
Pre-op hair removal
Type of procedure
Duration of procedure
SURGICAL CONSCIENCE
Surgical conscience is the practice of strict adherence to aseptic technique by ALL surgical team members, including YOU, the SURGICAL TECHNOLOGIST!
Also includes: Honesty, moral integrity, responsibility Ability to recognize and correct breaks in aseptic technique If there is hesitation and/or inability to admit = there is no place for you
in the O.R. Following all standard precautions at all times
There can be no compromise of aseptic technique
BASIC TERMINOLOGY
Antiseptic
Asepsis
Bacteriocide
Bacteriostatic
Bioburden
Contamination
Cross-contamination
BASIC TERMINOLOGY (CONT.)
Decontamination
Disinfectant
Event-related sterility
Fomite
Fungicide
Infection
Nosocomial
BASIC TERMINOLOGY (CONT.)
Sterile technique
Sterilization
Strike-through contamination
Surgically clean
Terminal disinfection
Terminal sterilization
Transient flora
Vector
Virucide
PRINCIPLES OF ASEPSIS
Principle 1: sterile field is created for each procedure
Principle 2: sterile team member must be appropriately attired prior to entering sterile field
Principle 3: movement in and around the sterile field must not compromise the sterile field
PRINCIPLE 1
Time
Instrument sets, peel packs, and wrappers
Chemical indicators
Sterile edges
Opening packages
Items that fall below table edges
Questionable sterility
Causes of contamination
PRINCIPLE 2
Sterile portion of gown
Sterile portion of table
Proper technique with arms and hands
Surface for gowning and gloving
Sitting during surgery
Platform standing
PRINCIPLE 3
Sterile to sterile
Sterile individuals keep within sterile area
Nonsterile to nonsterile
MORPHOLOGY
Bacillus- rod shape
Spirilla- spiral shape
L-Form- bacteria that lose normal shape (environmental)
NUTRITIONAL/02 REQUIREMENTS
Classifications: ex) oxygen, carbon, nitrogen
- obligate aerobes
-microaerophiles
-obligate anaerobes
-facultative anaerobes
-aerotolerant anaerobes
-capnophiles
PATHOGENICITY
Ability to cause disease
- release of exotoxins and endotoxins
- release of enzymes
- presence of a protective capsule
- attachment to host cell
METABOLISM, PROTEINS, AND GENETICS
Metabolism is the secretion of waste products
Proteins specific to bacterial species
DNA is unique to each bacteria species
SPORE FORMING
Bacterial species capable of forming spores
Unfavorable conditions = cell is enclosed in a protein capsuleto
High survival
NOT REPRODUCTION
Difficult to destroy
DISINFECTION, DECONTAMINATION, AND STERILIZATION
Disinfection process in which most but NOT ALL the microorganisms on INANIMATE
are destroyed
Decontamination Antisepsis: process in which most but NOT ALL microorganisms on
ANIMATE surfaces are destroyed Antiseptic: solutions
Sterilization destruction of ALL microorganisms, including SPORES, on inanimate
surfaces
DISINFECTION PRINCIPLES AND DISINFECTING AGENTS
Cleaning physical removal of blood and body fluids, as well as BIOBURDEN, from inanimate objects.
Disinfection high, intermediate, and low levels
Sterilization steam, chemical agents, high velocity electron bombardment, and
ultraviolet radiation critical, semi-critical, and noncritical
DISINFECTANT EFFICIENCY FACTORS
Concentration level of disinfectant solution
Number and type of microbes present
Physical factors of the solution
- temperature
- water hardness
- pH level
- exposure time
ALWAYS FOLLOW MANUFACTURER’S INSTRUCTIONS!
HIGH LEVEL DISINFECTANT COMPOUNDS
Glutaraldehyde/Cidex pH: 7.5-6.5 Best overall disinfectant/liquid sterilant Complete immersion in liquid Endoscopes Shelf life of 14 days/28 days
HIGH LEVEL DISINFECTANT COMPOUNDS
Sodium hypochlorite Household bleach Disinfectant for surfaces, floors, and equipment CDC recommended on blood and body fluid spills
INTERMEDIATE LEVEL DISINFECTANT COMPOUND
Phenol Carbolic acid Large areas and general basis
Quaternary Ammonium Compounds “quats” Bactericidal, fungicidal, pseudomonacidal Not sporicidal or tuberculocidal Common: benzalkonium chloride, dimethyl benzyl ammonium chloride
and the newer, diakyl quat
Alcohol Isopropyl and ethyl alcohol: diluted 60-70% Bactericidal, virucidal, fungicidal, tuberculocidal, NOT sporicidal
ENVIRONMENTAL DECONTAMINATION
Role: minimize microbial counts in the OR environment
Surfaces and characteristics
Pre-op, intra-op and post-op
Standard precautions and PPE
ENVIRONMENTAL SERVICES
Decontamination practices in the OR pre, intra, post, or between
Terminal cleaning
Weekly cleaning
Dirty cases
SURGICAL INSTRUMENT DECONTAMINATION PROCESS
ALL ITEMS USED ON STERILE FIELD AND/OR ON OPEN TISSUE MUST BE STERILIZED!
Decontamination is the first step Cleaning Disinfected Lubricated (if necessary) Sorted Reassembled Wrapped Sterilized Stored properly
CLEANING
Presoaking in basin Sterile water Enzymatic solution
Proteolytic enzymatic cleaner Lipolytic enzymatic cleaner
Detergent solutions Table 7-8
Rinsed and dried Chelation, enzymatic, emulsification, and solubilization
Table 7-9
MANUAL CLEANING
1. Instruments immersed in a solution. Friction will loosen organic material. With stainless steel: back and forth motion; circular can scratch.
2. Rinse in distilled water. NO TAP WATER!
3. AVOID spotting the instruments, so DRY!
DECONTAMINATION
Washer-sterilizer
Washer decontaminator
Ultrasonic washer Considerations:
Use of tray- perforated/wire mesh Heavier instruments place on the bottom Hinges left open Disassemble any instrument Concave surfaces should be placed upside down
WASHER DECONTAMINATOR
“WD”
Purpose: allows for hands-off processing
Considered “clean” but DOES NOT INCLUDE STERILIZING PHASE
WASHER STERILIZER
“WS”
Stainless steel and heat tolerated items
MUST BE CLEAN BEFORE USE!
Stainless steel must not be placed near other metals = fusion
Use free rinsing, low sudsing, neutral pH detergent
NOT USED DIRECTLY ON PATIENTS NOT A BIOLOGICALLY MONITORED PROCESS
Types of WS machines Tunnel like chamber Horizontal/cabinet type Gravity cycle of 270 degrees
ULTRASONIC CLEANER
After instruments are placed in WD or WS, they’re place in the ultrasonic cleaner
Removes small organic particles, or places that cannot be reached Box locks, serrations, and ratchets
Cavitation High frequency sound waves Molecules are forced in a rapid motion which form bubbles Implosion occurs to create a vacuum, dislodging particles
Metal mesh trays
Each cycle last 4-5 minutes