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Sterilization & Disinfection
1
Outline
• Overview of disinfection
and sterilization.
• Various methods.
• Important perspectives.
Definitions
3
Sterilization: complete killing of all forms of
microorganisms, including bacterial spores.
Disinfection: killing or removing of harmful
vegetative microorganisms.
Antiseptic: disinfectant that can be safely used
on living tissues.
Definitions
4
Bacteriocide
kill microbes
also germicide, fungicide, virucide
Bacteriostatic
Prevents or stops microbial growth
also fungistatic, virustatic
Aseptic(Asepsis)
Prevent contamination of person or object
by microbes
Definitions
• Sanitize
–Removal of pathogens from inanimate
objects
–Mechanical or chemical cleaning
–need not sterilize of disinfect
• Contamination
–Presence of living microbes on object
History
• In 1862, Louis Pasteur
developed pasteurization
process.
• Joseph Lister,
in 1867, used a carbolic
solution spray on the
wounds of his patients.
• Charles Chamberland,
developed the first
pressure steam sterilizer,
or autoclave in 1876.
Getting from here…
7
Back To Here:
8
Survival of Pathogens on
Surfaces
Pathogen Survival
MRSA 7 days – 7 months
VRE 5 days – 4 months
Acinetobacter 3 days -5 months
C. difficile (spores) 5 months
Norovirus 12 – 28 days
HIV Minutes to hours
HBV 7 days
HCV 16 hours – 4 days
Order of resistance
10
Hardest to Kill
•Prions
•Spores
•Mycobacteria
•Non-enveloped viruses
•Fungi
•Vegetative bacteria
•Enveloped viruses
Easiest to Kill
Methods of sterilization
and disinfection
PHYSICAL METHODS CHEMICAL METHODS
•SUNLIGHT
• DRYING
• DRY HEAT
• MOIST HEAT
• FILTRATION
• RADIATION
•ULTRASONIC AND
SONIC
VIBRATIONS
•ALCOHOLS
• ALDEHYDES
• DYES
• HALOGENS
• PHENOLS
•SURFACE-ACTIVE
AGENTS
• METALLIC SALTS
• GASES
Choice of Method
• Method to be used will
depend on:
–Device’s intended use
–Risk of infection
–Degree of soilage
• Process must not damage
the device
Spaulding Classification
Management of
contaminated items
14
Contaminated reusable items
should be:
•Handled as little as possible
•Staff should wear appropriate
PPE
•Gross debris removed at point
of use
•Soiled items removed
immediately after use
It all starts with cleaning
15
Items can’t be
or
disinfected
sterilized unless
they are properly
cleaned.
Cleaning instruments
16
•Soak in enzymatic or non-
enzymatic detergent
•Wear the appropriate PPE
•Keep instruments submerged
in solution and scrub with
brush
•Thoroughly rinse the
instrument
•Allow instrument to dry
Automated cleaning
17
Types:
• Ultrasonic cleaner
• Instrument washer
Benefits:
• Improved efficacy
• Reduced employee
exposure to splash and
sharps
Disinfectants
Activity of disinfectants
19
•Contamination
•Concentration
•Temperature
•Time
•Range of action
High-Level Disinfectants
Germicide Concentration
Glutaraldhyde (Cidex) ≥ 2.0%
Ortho-phthaladehyde (Cidex OPA) 0.55%
Hydrogen Peroxide* (Sporox) 7.5%
Hydrogen Peroxide and peracetic acid* (Peract) 1.0% / 0.08%
Hydrogen Peroxide and peracetic acid* (Endospore
+)
7.5% / 0.23%
Hypochlorite (free chlorine)* (Sterilox ©) 650-675 ppm
Accelerated hydrogen peroxide (Resert XL) 2.0%
Peracetic Acid (Steris 20) 0.2%
Glutaraldehyde and Isopropanol (Aldahol III) 3.4% / 26%
Glutaraldehyde and phenol/phenate (Sporicidin) 1.21% / 1.93%
Liquid Disinfectants
Disinfectant Agent Use Concentration
Ethyl or isopropyl alcohol 70% - 90%
Chlorine (bleach) 100 ppm
Phenolic UD
Iodophor UD
Quaternary ammonium
compound (QUAT)
UD
Improved/Accelerated hydrogen
peroxide
0.5%, 1.4%
Sterilization
Dry Heat Sterilisation
• Require hot-air ovens
• For glassware, metallic items, powders and
oil/grease
• Time two hours at 160°C and one hour at
180°C
• Plastics, rubber, paper and cloth cannot be
placed in them due to fire risk
Dry Heat Sterilisation
Advantages
• Can be used for powders, anhydrous oils
• Inexpensive
• No corrosive effect on instruments
Disadvantages
• High temperature damages some items
• Penetration of heat slow, uneven
Autoclave
Pressure
(psi)
Temperature
(°C)
Time
(mins)
15 121 15
20 126 10
20 134 3
Types of autoclave
• Downward displacement
• Positive pressure
displacement
• Negative pressure
displacement
• Triple vacuum autoclave
Gravity Displacement
Autoclaves
• Steam introduced to purge
out air and build pressure
• Raise temperature normally
to 121°C at 15 pounds/square
inch and maintain it for 15-45
minutes
• For sterilising liquids and
items in wraps that steam can
penetrate
High-Vacuum Autoclaves
• Air is first vacuumed out and
then steam introduced
• Faster and better penetration
throughout the load
• Pressure and temperature
higher; 134°C at about at 30
pounds/inch2
• Processing time about three
minutes
• Not suited for liquids due to
need for vacuum
Low-Temperature
Sterilization
• Mixture of steam (50-80°C) and
formaldehyde vapour
• Toprocess heat-resistant or heat-
sensitive medical devices in
specialised equipment
• Devices pre-cleaned and wrapped in
standard material and processed in
a three-hour cycle
• Cannot be used for liquids
• Formaldehyde must be purged/
neutralised well
Flash Sterilisation
Only to process a critical surgical
item:
in an emergency
when accidentally
contaminated, or
when other means of
sterilisation unavailable
Never to be used for implantable
items or to compensate for
shortage of key instruments
Ethylene Oxide Gas
Sterilisation
• Used for heat or
moisture
sensitive items
• Prevents normal
cellular
metabolism and
replication
Hydrogen Peroxide Gas Plasma
• Highly reactive/charged particles
from hydrogen peroxide generated
under vacuum
• Can be used to sterilise heat- and
moisture-sensitive items
– Some plastics, electrical/electronic
devices, and corrosion-susceptible
metal alloys
• Special wrapping required
Fumigation
• For rooms contaminated with some
pathogens
– Such as MRSA and Clostridium difficile
• Release of hydrogen peroxide, chlorine
dioxide gas or possibly ozone in sealed
rooms
• Spore strips (biological indicators)
placed strategically to monitor process
• Special equipment required
• Risk of damage to sensitive items
Pasteurisation and Boiling
• Semi-critical items can be
pasteurised
– 65-77°C, 30 min
– Example: respiratory therapy
equipment
• Must be retrieved carefully for
safe transport and storage
Filtration
• Removal of microbes from air
or heat-sensitive liquids
• Disinfectant-impregnated
filters may inactivate trapped
microorganisms
• Example: High-efficiency
particulate air (HEPA) filters
• All filters must be checked for
integrity and replaced as
necessary
Ultraviolet (UV) Light
• UV lamps useful for
chemical-free
disinfection of air and
water and also possibly
for decontamination of
environmental surfaces
• Broad-spectrum
microbicidal action
• Require regular cleaning
and periodic
replacement
Microwaves
• Heating from rapid rotation of
water molecules
• Limited use except for disinfecting
soft contact lenses and urinary
catheters for intermittent self-
catheterisation
• May be used in emergencies to
treat water for drinking or to
‘disinfect’ small water-immersible
plastic or glass items
Wrapped or Packaged
Instrument Sets in
Autoclave
39
Item Time Temperature Pressure Notes
Small wrapped
or
packaged loads
15 minutes
Add 5 min to
allow for
reaching
parameters
270° F (132°C) 30 psi Drying time 15-30 min
No drying time – packs
must be handled with
sterile gloves
*Not recommended without use of minimum drying times
Instrument wrap
40
• Should be square wrap with
a 6 inch border around each
side of the pan.
• Alternative wrap: 140-
thread count, 100% cotton
muslin.
Wet packs?
41
Cause Solution
Over packed autoclave Run smaller loads
Dehydrated wrap Launder wrap after each
use
Short drying time Extend drying times
Stored on solid cool
surface
Store on wire mesh
shelving
Storage of Sterile Items
42
•A well-ventilated area that provides
protection against dust, moisture, and
temperature and humidity extremes.
•Sterile items should be stored so that
packaging is not compromised.
•Label sterilized items with a load
number that indicates the sterilizer
used, the cycle or load number, the
date of sterilization, and if applicable
the expiration date.
Monitoring
43
Autoclave tape – external
indicator
Chemical indicator – internal
indicator
Indicators should be checked prior to using any item.
No color change – do not use and return for proper sterilization.
Biological monitors
METHOD OF
STERILIZATION
BIOLOGICAL CONTROL
•Hot Air Oven Bacillus subtilis subsp. Niger
Clostridium tetani
• Autoclave Bacillus stearothermophilus
•Filtration Serratia marcescens,
Pseudomonas diminuta
• Ionizing Radiation
Bacillus pumilis
Dental Surgery Perspective
45
Gigasept which contains
succindialdehyde and
dimethoxytetrahydrofuran
are used for disinfection
of plastic and rubber
materials eg: dental chair
Asepsis of surgical theaters
Fumigation is done by
two methods:
• Electric boiler
method
• Potassium
permanganate
BIOPSY SPECIMEN
Biopsy collection &
transportation can also be a
source of infection.
• It should be kept in sturdy
containers with secure lid.
• Avoid contaminating the
external surface of the
container.
• Swab used for collecting micro-
organisms should be
transferred slowly and carefully
to the swab container
Impression Trays
Impression trays are sterilized as follows
• metallic - autoclave
• plastic – ethylene oxide
Disinfection of alginate impressions –
Methods
• - Spraying
• - Immersion
• Iodophors, sodium hypochlorite (1:10
concentration ) ,
• phenols, formaldehyde, glutaraldehyde.
DENTAL CASTS
Spraying until wet or
Immersing in a 1:10
dilution of sodium
hypochlorite or an
iodophor then rinse
Casts to be disinfected
should be fully set (i.e.
stored for at least 24
hours
ROTARY INSTRUMENTS - BURS
Diamond and carbide burs:
After use they are placed in 0.2%
gluteraldehyde and sodium phenate (Eg.
Sporicidin) for at least 10 minutes,
cleaned with a bur brush or in an ultrasonic
bath.
Sterilize in an autoclave or dry heat
Steel burs:
May get damaged by autoclaving. Can be
sterilized by using a chemical vapor sterilizer or
glass bead sterilizer at 2300C for 20-30 seconds.
INSTRUMENTS
Sharp instruments are ideally sterilized by :
conventional hot air oven
BUT NOT BY:
Boiling
Autoclave
2% glutaraldehyde
Blunt instruments are sterilized by
Autoclave
Sutures
Sutures are pre sterilized by
gamma radiation
Sutures are re- sterilized by two
recommended methods
1. Soak for a full 10 minutes
completely immersed in
povidone iodine 10% solution,
then rinse in sterile
saline/water.
2. Ethylene Oxide – gas
sterilisation.
ENDODONTIC INSTRUMENTS
• Glass Bead or salt sterilizer
• Gutta percha points are pre-
sterilized.
• Contaminated points are
sterilized by 5.25% sodium
hypochlorite(1 min immersion).
Then rinse with hydrogen peroxide
& dry it.
IMPLANTS
Pre sterilized with Gamma
radiation
In case the implants needs to be
re-sterilized conventional
sterilization techniques are not
satisfactory
Steam / Dry heat sterilization
should not be used
Radio frequency glow discharge
technique (RFGDT) or Plasma
cleaning is used.
Take home points
55
Cleaning, disinfection, and sterilisation are
the backbone of infection prevention and
control
Proper cleaning is essential before any
disinfection or sterilisation process
Take home points
56
Steam sterilisation is effective only when
preceded by
Thorough pre-cleaning, proper
packaging/loading, and careful
monitoring of autoclaves.
Chemical disinfectants must be selected,
used, and discarded to minimise harm.
References
• Yoo JH. Principle and perspective of healthcare-associated infection control. J Korean Med Assoc. 2018;61:5–12.
• Stokes HW,Gillings MR. Gene flow, mobile genetic elements and the recruitment of antibiotic resistance genes into
Gram-negative pathogens. FEMS Microbiol Rev. 2011;35:790–819.
• Rutala WA, Weber DJ. Disinfection, sterilization, and antisepsis: An overview. Am J Infect
Control. 2016;44(Suppl):e1–e6.
• McDonnell G, Russell AD. Antiseptics and disinfectants: activity, action, and resistance. Clin Microbiol
Rev. 1999;12:147–179.
• Rutala WA, Weber DJ. Disinfection and sterilization in health care facilities: what clinicians need to know. Clin Infect
Dis. 2004;39:702–709.
• Rutala WA, Weber DJ. Disinfection and sterilization in health care facilities: an overview and current issues. Infect
Dis Clin North Am. 2016;30:609–637.
• Cadenas E. Biochemistry of oxygen toxicity. Annu Rev Biochem. 1989;58:79–110.
• Hayyan M, Hashim MA, AlNashef IM. Superoxide ion: generation and chemical implications. Chem
Rev. 2016;116:3029–3085.
• Russell AD. Bacterial spores and chemical sporicidal agents. Clin Microbiol Rev. 1990;3:99–119.
• Alexander’s Care of the Patient in Surgery, Jane C. Rothrock, 15th edition, Mosby Elsevier, 2015.
• Berry & Kohn’s Operating Room Technique, Nancymarie Phillips, 12th edition, Mosby Elsevier, 2012.
• Essentials of Perioperative Nursing, Goodman and Spry, 5th edition, Jones and Bartlett Learning, 2014.
• Perioperative Standards and Recommended Practice, Association of Perioperative Registered Nurses (AORN), 2014
edition.
• Surgical Technology for the Surgical Technologist: A Positive Care Approach, American Association of Surgical
Technologist (AST), 4th edition, Delmar, 2012.
Questions ?

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sterilization & disinfectiono- lecture 5.pptx

  • 2. Outline • Overview of disinfection and sterilization. • Various methods. • Important perspectives.
  • 3. Definitions 3 Sterilization: complete killing of all forms of microorganisms, including bacterial spores. Disinfection: killing or removing of harmful vegetative microorganisms. Antiseptic: disinfectant that can be safely used on living tissues.
  • 4. Definitions 4 Bacteriocide kill microbes also germicide, fungicide, virucide Bacteriostatic Prevents or stops microbial growth also fungistatic, virustatic Aseptic(Asepsis) Prevent contamination of person or object by microbes
  • 5. Definitions • Sanitize –Removal of pathogens from inanimate objects –Mechanical or chemical cleaning –need not sterilize of disinfect • Contamination –Presence of living microbes on object
  • 6. History • In 1862, Louis Pasteur developed pasteurization process. • Joseph Lister, in 1867, used a carbolic solution spray on the wounds of his patients. • Charles Chamberland, developed the first pressure steam sterilizer, or autoclave in 1876.
  • 9. Survival of Pathogens on Surfaces Pathogen Survival MRSA 7 days – 7 months VRE 5 days – 4 months Acinetobacter 3 days -5 months C. difficile (spores) 5 months Norovirus 12 – 28 days HIV Minutes to hours HBV 7 days HCV 16 hours – 4 days
  • 10. Order of resistance 10 Hardest to Kill •Prions •Spores •Mycobacteria •Non-enveloped viruses •Fungi •Vegetative bacteria •Enveloped viruses Easiest to Kill
  • 11. Methods of sterilization and disinfection PHYSICAL METHODS CHEMICAL METHODS •SUNLIGHT • DRYING • DRY HEAT • MOIST HEAT • FILTRATION • RADIATION •ULTRASONIC AND SONIC VIBRATIONS •ALCOHOLS • ALDEHYDES • DYES • HALOGENS • PHENOLS •SURFACE-ACTIVE AGENTS • METALLIC SALTS • GASES
  • 12. Choice of Method • Method to be used will depend on: –Device’s intended use –Risk of infection –Degree of soilage • Process must not damage the device
  • 14. Management of contaminated items 14 Contaminated reusable items should be: •Handled as little as possible •Staff should wear appropriate PPE •Gross debris removed at point of use •Soiled items removed immediately after use
  • 15. It all starts with cleaning 15 Items can’t be or disinfected sterilized unless they are properly cleaned.
  • 16. Cleaning instruments 16 •Soak in enzymatic or non- enzymatic detergent •Wear the appropriate PPE •Keep instruments submerged in solution and scrub with brush •Thoroughly rinse the instrument •Allow instrument to dry
  • 17. Automated cleaning 17 Types: • Ultrasonic cleaner • Instrument washer Benefits: • Improved efficacy • Reduced employee exposure to splash and sharps
  • 20. High-Level Disinfectants Germicide Concentration Glutaraldhyde (Cidex) ≥ 2.0% Ortho-phthaladehyde (Cidex OPA) 0.55% Hydrogen Peroxide* (Sporox) 7.5% Hydrogen Peroxide and peracetic acid* (Peract) 1.0% / 0.08% Hydrogen Peroxide and peracetic acid* (Endospore +) 7.5% / 0.23% Hypochlorite (free chlorine)* (Sterilox ©) 650-675 ppm Accelerated hydrogen peroxide (Resert XL) 2.0% Peracetic Acid (Steris 20) 0.2% Glutaraldehyde and Isopropanol (Aldahol III) 3.4% / 26% Glutaraldehyde and phenol/phenate (Sporicidin) 1.21% / 1.93%
  • 21. Liquid Disinfectants Disinfectant Agent Use Concentration Ethyl or isopropyl alcohol 70% - 90% Chlorine (bleach) 100 ppm Phenolic UD Iodophor UD Quaternary ammonium compound (QUAT) UD Improved/Accelerated hydrogen peroxide 0.5%, 1.4%
  • 23. Dry Heat Sterilisation • Require hot-air ovens • For glassware, metallic items, powders and oil/grease • Time two hours at 160°C and one hour at 180°C • Plastics, rubber, paper and cloth cannot be placed in them due to fire risk
  • 24. Dry Heat Sterilisation Advantages • Can be used for powders, anhydrous oils • Inexpensive • No corrosive effect on instruments Disadvantages • High temperature damages some items • Penetration of heat slow, uneven
  • 26. Types of autoclave • Downward displacement • Positive pressure displacement • Negative pressure displacement • Triple vacuum autoclave
  • 27. Gravity Displacement Autoclaves • Steam introduced to purge out air and build pressure • Raise temperature normally to 121°C at 15 pounds/square inch and maintain it for 15-45 minutes • For sterilising liquids and items in wraps that steam can penetrate
  • 28. High-Vacuum Autoclaves • Air is first vacuumed out and then steam introduced • Faster and better penetration throughout the load • Pressure and temperature higher; 134°C at about at 30 pounds/inch2 • Processing time about three minutes • Not suited for liquids due to need for vacuum
  • 29. Low-Temperature Sterilization • Mixture of steam (50-80°C) and formaldehyde vapour • Toprocess heat-resistant or heat- sensitive medical devices in specialised equipment • Devices pre-cleaned and wrapped in standard material and processed in a three-hour cycle • Cannot be used for liquids • Formaldehyde must be purged/ neutralised well
  • 30. Flash Sterilisation Only to process a critical surgical item: in an emergency when accidentally contaminated, or when other means of sterilisation unavailable Never to be used for implantable items or to compensate for shortage of key instruments
  • 31. Ethylene Oxide Gas Sterilisation • Used for heat or moisture sensitive items • Prevents normal cellular metabolism and replication
  • 32. Hydrogen Peroxide Gas Plasma • Highly reactive/charged particles from hydrogen peroxide generated under vacuum • Can be used to sterilise heat- and moisture-sensitive items – Some plastics, electrical/electronic devices, and corrosion-susceptible metal alloys • Special wrapping required
  • 33. Fumigation • For rooms contaminated with some pathogens – Such as MRSA and Clostridium difficile • Release of hydrogen peroxide, chlorine dioxide gas or possibly ozone in sealed rooms • Spore strips (biological indicators) placed strategically to monitor process • Special equipment required • Risk of damage to sensitive items
  • 34. Pasteurisation and Boiling • Semi-critical items can be pasteurised – 65-77°C, 30 min – Example: respiratory therapy equipment • Must be retrieved carefully for safe transport and storage
  • 35. Filtration • Removal of microbes from air or heat-sensitive liquids • Disinfectant-impregnated filters may inactivate trapped microorganisms • Example: High-efficiency particulate air (HEPA) filters • All filters must be checked for integrity and replaced as necessary
  • 36. Ultraviolet (UV) Light • UV lamps useful for chemical-free disinfection of air and water and also possibly for decontamination of environmental surfaces • Broad-spectrum microbicidal action • Require regular cleaning and periodic replacement
  • 37. Microwaves • Heating from rapid rotation of water molecules • Limited use except for disinfecting soft contact lenses and urinary catheters for intermittent self- catheterisation • May be used in emergencies to treat water for drinking or to ‘disinfect’ small water-immersible plastic or glass items
  • 38. Wrapped or Packaged Instrument Sets in Autoclave 39 Item Time Temperature Pressure Notes Small wrapped or packaged loads 15 minutes Add 5 min to allow for reaching parameters 270° F (132°C) 30 psi Drying time 15-30 min No drying time – packs must be handled with sterile gloves *Not recommended without use of minimum drying times
  • 39. Instrument wrap 40 • Should be square wrap with a 6 inch border around each side of the pan. • Alternative wrap: 140- thread count, 100% cotton muslin.
  • 40. Wet packs? 41 Cause Solution Over packed autoclave Run smaller loads Dehydrated wrap Launder wrap after each use Short drying time Extend drying times Stored on solid cool surface Store on wire mesh shelving
  • 41. Storage of Sterile Items 42 •A well-ventilated area that provides protection against dust, moisture, and temperature and humidity extremes. •Sterile items should be stored so that packaging is not compromised. •Label sterilized items with a load number that indicates the sterilizer used, the cycle or load number, the date of sterilization, and if applicable the expiration date.
  • 42. Monitoring 43 Autoclave tape – external indicator Chemical indicator – internal indicator Indicators should be checked prior to using any item. No color change – do not use and return for proper sterilization.
  • 43. Biological monitors METHOD OF STERILIZATION BIOLOGICAL CONTROL •Hot Air Oven Bacillus subtilis subsp. Niger Clostridium tetani • Autoclave Bacillus stearothermophilus •Filtration Serratia marcescens, Pseudomonas diminuta • Ionizing Radiation Bacillus pumilis
  • 44. Dental Surgery Perspective 45 Gigasept which contains succindialdehyde and dimethoxytetrahydrofuran are used for disinfection of plastic and rubber materials eg: dental chair
  • 45. Asepsis of surgical theaters Fumigation is done by two methods: • Electric boiler method • Potassium permanganate
  • 46. BIOPSY SPECIMEN Biopsy collection & transportation can also be a source of infection. • It should be kept in sturdy containers with secure lid. • Avoid contaminating the external surface of the container. • Swab used for collecting micro- organisms should be transferred slowly and carefully to the swab container
  • 47. Impression Trays Impression trays are sterilized as follows • metallic - autoclave • plastic – ethylene oxide Disinfection of alginate impressions – Methods • - Spraying • - Immersion • Iodophors, sodium hypochlorite (1:10 concentration ) , • phenols, formaldehyde, glutaraldehyde.
  • 48. DENTAL CASTS Spraying until wet or Immersing in a 1:10 dilution of sodium hypochlorite or an iodophor then rinse Casts to be disinfected should be fully set (i.e. stored for at least 24 hours
  • 49. ROTARY INSTRUMENTS - BURS Diamond and carbide burs: After use they are placed in 0.2% gluteraldehyde and sodium phenate (Eg. Sporicidin) for at least 10 minutes, cleaned with a bur brush or in an ultrasonic bath. Sterilize in an autoclave or dry heat Steel burs: May get damaged by autoclaving. Can be sterilized by using a chemical vapor sterilizer or glass bead sterilizer at 2300C for 20-30 seconds.
  • 50. INSTRUMENTS Sharp instruments are ideally sterilized by : conventional hot air oven BUT NOT BY: Boiling Autoclave 2% glutaraldehyde Blunt instruments are sterilized by Autoclave
  • 51. Sutures Sutures are pre sterilized by gamma radiation Sutures are re- sterilized by two recommended methods 1. Soak for a full 10 minutes completely immersed in povidone iodine 10% solution, then rinse in sterile saline/water. 2. Ethylene Oxide – gas sterilisation.
  • 52. ENDODONTIC INSTRUMENTS • Glass Bead or salt sterilizer • Gutta percha points are pre- sterilized. • Contaminated points are sterilized by 5.25% sodium hypochlorite(1 min immersion). Then rinse with hydrogen peroxide & dry it.
  • 53. IMPLANTS Pre sterilized with Gamma radiation In case the implants needs to be re-sterilized conventional sterilization techniques are not satisfactory Steam / Dry heat sterilization should not be used Radio frequency glow discharge technique (RFGDT) or Plasma cleaning is used.
  • 54. Take home points 55 Cleaning, disinfection, and sterilisation are the backbone of infection prevention and control Proper cleaning is essential before any disinfection or sterilisation process
  • 55. Take home points 56 Steam sterilisation is effective only when preceded by Thorough pre-cleaning, proper packaging/loading, and careful monitoring of autoclaves. Chemical disinfectants must be selected, used, and discarded to minimise harm.
  • 56. References • Yoo JH. Principle and perspective of healthcare-associated infection control. J Korean Med Assoc. 2018;61:5–12. • Stokes HW,Gillings MR. Gene flow, mobile genetic elements and the recruitment of antibiotic resistance genes into Gram-negative pathogens. FEMS Microbiol Rev. 2011;35:790–819. • Rutala WA, Weber DJ. Disinfection, sterilization, and antisepsis: An overview. Am J Infect Control. 2016;44(Suppl):e1–e6. • McDonnell G, Russell AD. Antiseptics and disinfectants: activity, action, and resistance. Clin Microbiol Rev. 1999;12:147–179. • Rutala WA, Weber DJ. Disinfection and sterilization in health care facilities: what clinicians need to know. Clin Infect Dis. 2004;39:702–709. • Rutala WA, Weber DJ. Disinfection and sterilization in health care facilities: an overview and current issues. Infect Dis Clin North Am. 2016;30:609–637. • Cadenas E. Biochemistry of oxygen toxicity. Annu Rev Biochem. 1989;58:79–110. • Hayyan M, Hashim MA, AlNashef IM. Superoxide ion: generation and chemical implications. Chem Rev. 2016;116:3029–3085. • Russell AD. Bacterial spores and chemical sporicidal agents. Clin Microbiol Rev. 1990;3:99–119. • Alexander’s Care of the Patient in Surgery, Jane C. Rothrock, 15th edition, Mosby Elsevier, 2015. • Berry & Kohn’s Operating Room Technique, Nancymarie Phillips, 12th edition, Mosby Elsevier, 2012. • Essentials of Perioperative Nursing, Goodman and Spry, 5th edition, Jones and Bartlett Learning, 2014. • Perioperative Standards and Recommended Practice, Association of Perioperative Registered Nurses (AORN), 2014 edition. • Surgical Technology for the Surgical Technologist: A Positive Care Approach, American Association of Surgical Technologist (AST), 4th edition, Delmar, 2012.