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INDIAN DENTAL ACADEMY
Leader in continuing dental education
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STERILIZATION
IN
ORTHODONTICS
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INTRODUCTION


KNOWLEDGE AND PRACTICE OF METHODS
USED FOR KILLING, REMOVING, OR
EXCLUDING MICROORGANISMS IS THE KEY
TO PREVENTION OF CROSS INFECTION IN
THE DENTAL CLINIC.
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STERILIZATION


Process by which all forms of
microorganisms including

viruses,bacteria fungi and spores over
articles or surfaces are destroyed.


Articles that are free of living organisms
are termed STERILE.
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DEFINITIONS --•ASEPSIS-a condition free of germs from
infection &any form of life.

•DISINFECT-To free from infection by physical
or chemical means.
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•DISINFECTION-Is used to describe a
process which reduces the number of
contaminating microorganisms particularly
those liable to cause infections,to a level
which is deemed no longer harmful to health.

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•ANTI SEPSIS-a term used to describe
disinfectant applied to living tissue such as a
wound.

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MODES OF TRANSMISSION
•FROM PATIENT TO PRACTITONER.
•FROM PRACTITONER TO PATIENT.

•FROM ONE PATIENT TO
ANOTHER(CROSS INFECTION).
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ROUTE OF TRANSMISSION
1.

INOCULATION –accidental self injury with a
contaminated needle,sharp insruments.
microorganisms transmitted –
HBV,HCV, HDV, HSV I ,HSV II, HIV,
NEISSERIA GONORRHOEA, TREPONEMA

PALLEDUM, CLOSTRIDIUM TETANI.

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2. INHALATION :INHALATION OF MICROORGANISMS
AEROSOLIZED FROM A PATIENT’S BLOOD OR SALIVA
OCCURS WHEN USING HIGH SPEED OR ULTRASONIC
EQUIPMENT.

Eg :VARICELLA ZOSTER ,CYTOMEGALOVIRUS ,RUBEOLA
& MUMPS VIRUS ,RUBELLA VIRUS , MYCOBACTERIUM

TUBERCULOSIS, CANDIDA ALBICANS.

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AREAS OF INFECTION CONTROL

•INFECTION CONTROL IN THE
CLINICAL AREA.
•INFECTION CONTROL IN THE
LABORATORY SET UP.

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INFECTION CONTROL IN CLINICAL AREA.

•PERSONAL PROTECTION EQUIPMENTS(PPE).
•ENVIRONMENTAL SURFACE CLEANING
&DISINFECTION .
•INSTRUMENT STERILIZATION.
•DISPOSAL OF WASTE.
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PERSONNEL PROTECTION EQUIPMENT
(PPE)
•Protective clothing.
•Gloves.
•Masks.
•Protective eyewear.
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CATEGORIES OF PERSONEL
•CAT 1-personnel routinely performs tasks that
involve exposure to blood or other potentially

infectious materials.
•CAT 2-are personnel who on occasion may

perform tasks that involve exposure to blood
and other potentially infectious materials.
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PROTECTIVE CLOTHING
•Primary function- Protect worker from exposure to
contaminated materials
•Fluid resistant.
•Minimal skin exposures,ie.long sleeves.
•Cuff of the sleeve covered by the band of the
•glove.

•High risk procedures need have at least knee length when
seated.
•Buttons ,zippers,should be hidden and not exposed.
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GUIDE LINES
•Protective clothing not to be worn outside
the dental office.
•Change at least daily.
•Incase soiled, change immediately.

•Remove while relaxing esp. in the cafeteria
while eating or drinking.
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GLOVES


Gloves should be used while touching ----

1.

Blood and body fluids.

2.

Mucous membrane.

3.

Non intact skin of the patient.

4.

Items or surfaces soiled with blood or body

fluids.

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Types of gloves
1.

2.

3.

4.

5.

Vinyl or latex sterile, single use surgical procedure.
Vinyl or latex - non sterile, single use examination procedure.

Rubber / plastic material - non
sterile,multiple use - over gloving.
Polyethylene - non-sterile,multiple use over gloving.
Nylon glove – non sterile ,multiple use –
using beneath gloves.
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General precautions to be
taken while using gloves








Wear gloves for all dental procedures
Discard gloves whenever they have
been contaminated.
Do not leave the clinic or walk around
wearing gloves.
Wash hands after removing gloves.
Used needles should not be recapped.
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REPROCESSING OF GLOVES







Rinse your gloved hands thoroughly in a
hypochlorite solution.
Then in clear water to remove the disinfectant.

Wash with soap and water and rinse
thoroughly.
Remove the gloves and hang them up by the
cuffs to dry



Dust glove powder on the inside of the gloves .



Test for holes in the house before reuse.



Autoclave the gloves.
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MASKS






Surgical masks / chin length plastic face
shields must be worn to protect the face.
Should have at least 95% filtration efficiency
for particles 3-5 micrometer in diameter.
Should be changed for each patient since its
efficiency decreases as it traps moisture
during dental procedures.

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EYE PROTECTION


The eyes of a dental professional are
particularly susceptible to physical &
microbial injury by virtue of their
limited vascularity and diminished
immune capacities.



Eyes must be protected during
operative procedures by spectacles.
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HAND WASHING

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•First scrub hands with warm water.
•Get soap under the nails and clean with brush.

•Rinse hands with cold water.
•Wipe hands with paper towel or dry with

warm air.
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AGENTS OF HAND CLEANING
•Substituted phenol preparations like
chlorhexidine gluconate and
parachlorometaxylenol (pcmx).
•4% chlorhexidine & 3% PCMX are equally
sufficient.

•Both remain in the tissues in an active form for
prolonged periods thus maintaining a residual
activity for prolonged periods.
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Method of sterilization


Moist heat (autoclaving)



Dry heat



Chemicals (chemiclaving)

(hot air oven)

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Moist heat
•Moist heat denatures & coagulates the
protein of microbes.
•Better than dry heat because of its higher
efficiency of penetration.
•Due to latent heat of vaporization present in
moist heat.
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TYPES OF AUTOCLAVES
POROUS LOAD AUTOCLAVES :

1.

Autocycled high pressure vacuum models



.


Air is evacuated from the metal chamber
by vacuum suction.



1210 C , AT 20 lb pressure for 30 min.



Towels ,suture materials,cotton rolls,
rubber gloves ,root canal instruments.
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SMALL BENCH TOP AUTOMATIC
AUTOCLAVE


Work on the principle of downward
displacement of air as a consequence of
steam entering at the top of the
chamber.



Temp of 136oc ,at 32 lb pressure for 5
min

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STERILIZATION CYCLE
Temperature

Time

Pressure

Unwrapped
instruments

134oc

3 min

30 psi

Wrapped
instruments

1210c

15-20
min

15 psi

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DRY HEAT


Less effective than moist heat



Higher temperatures ,longer periods &longer

heating up time required for sterilization (45 min
to reach 160oc).


Should have a time clock on the door ,so items
cannot be added or removed during the cycle & a
fan to distribute the heat evenly.
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CHEMICAL STERILIZATION


Combination of formaldehyde,alcohol,acetone,ketone &steam at
20 psi serves as an effective sterilizing agent.



biocidal action of formaldehyde depends on its alkylation of
microbial nucleic acids,which control protein synthesis.



Takes longer time than an autoclave (30 min)for packaged
instruments (shorter than hot air oven)

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Advantage of chemiclave :


Shorter cycle



Lack of corrosion of instruments /burs.



Adequate ventilation must be provided
in order to expel the residual fumes

released on opening the chamber at the
end of the cycle.
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Ethylene oxide gas
sterilization.


A flammable ,explosive and toxic gas to which
all types of microbes are susceptible.



Biocidal activity is due to alkylation and hence

causes denaturation of microbial nucleic acid.


Biocidal activity increases in the presence of
moisture.



Plastic ,metal,rubber or cloth can be sterilized
without damage.



Equipment is costly & gas is toxic.
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STERILIZATION BY GAMMA
IRRADIATION :
 Used for needle,sutures ,gloves etc
GLASS BEAD STERILIZATION :


Heating glass beads in a chamber into
which instrument is inserted for 10-30
sec.



2100c –230 0c .



Suitable for very small instruments like
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R.C.T instruments ,burs ,pliers etc.
Water boilers…
•does not achieve sterilization as many spores
can with stand it.
•Cross infection from contaminated water
containing bacterial spores not killing by
boiling.
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Monitoring sterilization
Three forms


physical monitoring.



Chemical monitoring.



Biological monitoring.

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

PHYSICAL MONITORING :Refers to periodical observation of

displays or gauges on the sterilizer
during a cycle to ensure the sterilization
process.
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Chemical monitoring.
1.

2.

Two types are available
process indicators :- consist of colour
changing material (liquid /paper) which
changes color upon exposure to appropriate
sterilization cycle.
TST strips (TIME ,STEAM,TEMPERATURE)
change color when all parameters have
been adequately achieved in the
sterilization cycle.

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BIOLOGICAL MONITORING.


Indicator used are heat resistant
bacterial spores (bacillus

stearothermophillus ,bacillus
subtilis )


If the spores are killed ,then less
resistant microbes are killed more
readily and sterility is achieved.
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Classification of instruments to
be sterilized


Critical



Semi critical



Non- critical

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Critical


Surgical other instruments used to penetrate
soft tissue / bone.



Should be sterilized after each use.
eg :-forceps ,scalpels,bone chisels,scaling
instruments,surgical burs.

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Semi critical


Instrument that do not penetrate soft tissue /
bone but contact oral tissues.
eg :-mirrors ,plastic instruments,burs etc.

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

Non critical :Items which do not come into contact

with body fluids.
eg:-light cure tips,glass slab,cement

spatula,orthodontic pliers,dapen
dish.

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Procedure before sterilization

•Pre soaking of instruments.
•Pre sterilization cleaning
•

manual

•

ultrasonic
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Presoaking
•Keeps instruments wet.
•Prevents drying of saliva &blood on the
instruments.
•Facilitating easy cleaning.

•solution used may be phenol or
gluteraldehyde.
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Pre sterilization cleaning.
1.
2.








Manual cleaning
Ultrasonic cleaning :Employ piezo-electric oscillators situated underneath
S.S enclosures to create oscillations in a fluid filled
tank.
Oscillations are transformed into a series of high
frequency sound waves, which cause intense
microscopic cavitation in the fluid.
Large number of these tiny bubbles collapse creating
minute vacuum areas which are responsible for the
scrubbing effect.
2 – 20 min
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ADVANTAGE OF ULTRASONIC CLEANING
OVER MANUAL CLEANING

•Increased efficacy.
•Reduced danger of aerosolization.
•Reduced incidence of instrument injuries.
•Increased tarnish removal and cleanliness.
•Reduction in manual labour.
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Sterilization trays
Three types
1.

Fully closed system.(with individually
packed items in commercially available
sterilization bags)

2.

Perforated trays.(with fitted covers wrapped
with sterilization paper)

3.

Open tray system.(sealed with a see
through sterilization bag)
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Cold sterilization





process of disinfecting instruments /
equipment by using a liquid chemical
germicide is called cold sterilization.
Used for heat sensitive instruments.
Aseptic rinsing with sterile water and drying
should follow this disinfection process.

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Disinfectants used in dentistry





Glutaraldehydes.
Chlorine compounds.
Iodophors.
Synthetic phenolics.

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Chemical disinfectants effective in
inactivating HIV


SODIUM HYPOCHLORITE (0.1 -0.5%)



CHLORAMINE 2% (TOSYL CHLORAMIDE SODIUM)



ETHANOL 70%



2 –PROPANOL 70% (ISOPROPYL ALCOHOL)



PROVIDONE IODINE 2.5%



FORMALDEHYDE 4%



GLUTARAL 2% (GLUTARALDEHYDE)



HYDROGEN PEROXIDE 6%

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GLUTARALDEHYDE


20 min. immersion in a 2% alkaline glutaraldehyde solution
- disinfection.



6 -10 hours immersion – sterilization.
properties :-



high biocidal activity.



Broad antimicrobial spectrum within 10-30 min.



Sporicial after 7-10 hrs. of exposure at room temperature.



Noncorrosive.



Penetrates blood, pus & organic debris.



Induces severe tissue irritation upon prolonged contact.



Discolors nickel coated impression trays & carbon steel
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Quaternary ammonium compounds.

Advantages :

Bactericidal against gram positive bacteria.



Non –irritating.



Economical.



Pleasant odor.
Disadvantages:-



inactivated by organic matter.



Can sometimes support gram negative bacteria.



Easily inactivated by presence of anionic detergents, soaps
&hard water.
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Chlorine compounds
Advantages :

Rapid antimicrobial action.



Effective in dilute solution.



Economical



Sodium hypochlorite is useful as a broad spectrum
bactericidal, virrucidal, tuberculocidal surface
disinfectant.
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Disadvantage:•Sporicidal effects noted only at high
concentration.
•Prepared solution has only limited shelf life.
•Activity diminished by presence of organic matter
& altered pH


Unpleasant odor



Irritates skin &eyes.



Can degrade plastic & rubber coated instruments.
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Chlorine dioxide
Advantages :

Instrument and environmental surface disinfectant
/sterilant



Rapid 3 min. disinfection ,6 hrs. sterilization.



Non-irritating and non-toxic.
Disadvantage:-



Must be prepared daily



Does not readily penetrate organic debris.



Only 24 hrs shelf life.
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Iodophors
Advantages:1.

Broad spectrum disinfectant, especially effective
against heavy viral contamination.

2.

Biocidal activity occurs within 3-30 min.

3.

Effective in dilute solution.

Disadvantages:1.

Not a sterilant.

2.

Unstable at high temperature.

3.

Must prepare daily.

4.

Inactivated by hard water.

5.

May discolor some light colored surfaces.

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Alcohols (70% isopropyl alcohol &70%
ethyl alcohol)
Advantages :1.

Rapidly bactericidal against most gram positive & gram
negative bacteria.

2.

Active against many lipophilic viruses

3.

Economical.

Disadvantages :1.

Ineffective against bacterial spores.

2.

Diminished activity in organic matter and tissue debris.

3.

Bactericidal activity diminished greatly.
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Synthetic phenols



They act as a protoplasmic poison which precipitate the
protein and destroy the cell wall.
Advantages:-

1.

synergistic effect instead of additive.

2.

Broad antimicrobial spectrum.

3.

Can be used on metal, glass, rubber &plastic.

4.

Less toxic & corrosive.

5.

Economical.

Disadvantages:1.

Not a sterilant

2.

No re-use life.

3.

Irritates skin & eyes.

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Two methods of surface asepsis.

• Cleaning & disinfecting the
contaminated surface.
• Preventing the surface from becoming
contaminated.

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Surface cover.
• Materials impervious to moisture.
• On surfaces difficult to clean.
• To be changed between patients.
(impervious- backed paper, aluminium foil /
plastic covers )
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Spray – wipe spray technique.
• Spray the surface.

• Wipe in systematic pattern contacting each
surface at least twice.
• Spray again.
• Allow solution to dry and then wipe in 10
minutes for proper disinfection.
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• The disinfectant used must be a hospital level

disinfectant ie.it should inactivate the Polio 2 virus and
Mycobacterium Tuberculosis .

• Isopropyl alcohol and quaternary ammonium
compounds are not recommended as they achieve less

level of surface wettability compared to that of water
based disinfectants.
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Disinfecting dental equipments.

• Hand piece
• 3 way syringe tips
• HVE tips

• aspirators

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Hand pieces
• Most are autoclavable.
• Depends on manufacturers guidelines.
• Prior cleaning and lubrication is mandatory.
• Hand piece is placed in autoclavable pouch
with TST strips.

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Steps for proper sterilization of hand pieces.
• Decontamination inside n outside.
• Rinse .
• Flush lines.

• Dry .
• Sterilize .

• Lubricate and run hand piece.
• Bag wrap.
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Suck –back devices / check valves on hand pieces



Suck –back devices prevent any residual water left in
the line from the previous patient, from going into next
patient’s operating field when the procedure starts.



Check valve is a simple gadget that will tell you
immediately if any retained water is coming back out of
the hand piece.



Both these devices can be fitted on to an older hand
pieces.
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Three way syringe tips / high velocity
evacuation tips / aspirators






3 –way syringe should be treated in the same manner as
hand piece.

HVE tips –metal tips are autoclavable. Plastic tips must
be disposed off after single use.
Aspirators –disinfectant flushes for the aspirators should
be done after each patient.

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Sterilization & disinfection of
individual articles.
Disinfection of dental impressions :ALGINATE:-iodophores / glutaraldehyde – 15 min.

LYSOL spray – 10 min.

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Burs
ethylene oxide 4-12 hours

autoclave.
carbon steel instruments
chemical vapour---20 min at 270 °f
ethylene oxide ----4-12hours
dry heat oven---60-120 min at 320°f

tungsten carbide instruments
chemical vapour---20 min at 270 °f
dry heat oven---60-120 min at 320°f
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Corrosion of instruments.
corrosion is an electrolytic process in which the contact of
two dissimilar metals sets up a potential difference
resulting in an electron flow.This flow leaves behind reactive
ions that readily combines with atmospheric oxygen to
form oxides (rust).
Corrosion resistance of orthodontic grade steel is directly
proportional to its carbon content and the chromium content
( PASSIVATION EFFECT)
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Sterilization in orthodontics.
David Drake(1997)JCO







Plastic items & heat sterilizable
cheek retractors – immerse in procide
(strelalization solution whish turns milky after
autoclaving)
Hand pieces & photographic mirrors – sterilized in a
kavo-klave
Plier racks & instruments are placed in a wire basket
& run through an ultrasonic cleaner containing rust
inhibiting non-ionic multipurpose ultrasonic cleaner .
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









Ultra-sonic solution should be changed
daily & covered during cleaning to
reduce aerosols.
Dried blood must be scrubbed off &
repeat ultrasonic cleaning .
Heavy duty nitril gloves are required for
handling contaminated instruments.
After cleaning instruments are dipped in
a sodium nitrite rust inhibitor
Auto clave for 20 min &20 min for
cooling.
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STERILIZATION OF NiTi WIRES


Heat sterilization is the most reliable method -

(Steam autoclaving at 1210C,15-20psi for 20
min)


Chemical sterilization are corrosive &attack

metals immersed in them
(2% acidic Glutaraldehyde)

•

STERILIZATION OF ORTHODONTIC BANDS:-15 SECONDS OF

GLASS BEAD STERILIZATION.(SMITH et
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al 1986 AJO)
CAUSES OF STERILIZATION
FAILURE (GEORGE 1993 JCO)


CYCLE TIME TOO SHORT



TEMPERATURE TOO LOW



FAILURE TO PREHEAT



FAULTY STERILIZER



INTERRUPTING OF CYCLE



OVERLOADING OF CHAMBER



INADEQUATE STAFF TRAINING



IMPROPER PRECLEANING, PACKAGING



FAILURE TO USE BIOLOGICAL INDICATOR
TESTING.
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Disposal of waste
•Its should be disposed in tamper proof
containers/ boxes.

•Its should be labeled as BIOHAZARD.
•Should be in tune with the existing laws of the
area.
•Sharp material should be stored in hard walled
leak proof containers ,red in color.
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Color coding for waste disposal
•Yellow

--- waste for incineration .

•Yellow with ---

waste for land fill .

black stripes
•Light blue--- for autoclaving before disposal

•Red

---human anatomical wastes.

•Black

---normal household wastes.
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CONCLUSION
PREVENTION IS BETTER THAN CURE

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Thank you
For more details please visit
www.indiandentalacademy.com

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Sterilization in orthodontics

  • 1. INDIAN DENTAL ACADEMY Leader in continuing dental education www.indiandentalacademy.com STERILIZATION IN ORTHODONTICS www.indiandentalacademy.com
  • 2. INTRODUCTION  KNOWLEDGE AND PRACTICE OF METHODS USED FOR KILLING, REMOVING, OR EXCLUDING MICROORGANISMS IS THE KEY TO PREVENTION OF CROSS INFECTION IN THE DENTAL CLINIC. www.indiandentalacademy.com
  • 3. STERILIZATION  Process by which all forms of microorganisms including viruses,bacteria fungi and spores over articles or surfaces are destroyed.  Articles that are free of living organisms are termed STERILE. www.indiandentalacademy.com
  • 4. DEFINITIONS --•ASEPSIS-a condition free of germs from infection &any form of life. •DISINFECT-To free from infection by physical or chemical means. www.indiandentalacademy.com
  • 5. •DISINFECTION-Is used to describe a process which reduces the number of contaminating microorganisms particularly those liable to cause infections,to a level which is deemed no longer harmful to health. www.indiandentalacademy.com
  • 6. •ANTI SEPSIS-a term used to describe disinfectant applied to living tissue such as a wound. www.indiandentalacademy.com
  • 7. MODES OF TRANSMISSION •FROM PATIENT TO PRACTITONER. •FROM PRACTITONER TO PATIENT. •FROM ONE PATIENT TO ANOTHER(CROSS INFECTION). www.indiandentalacademy.com
  • 8. ROUTE OF TRANSMISSION 1. INOCULATION –accidental self injury with a contaminated needle,sharp insruments. microorganisms transmitted – HBV,HCV, HDV, HSV I ,HSV II, HIV, NEISSERIA GONORRHOEA, TREPONEMA PALLEDUM, CLOSTRIDIUM TETANI. www.indiandentalacademy.com
  • 9. 2. INHALATION :INHALATION OF MICROORGANISMS AEROSOLIZED FROM A PATIENT’S BLOOD OR SALIVA OCCURS WHEN USING HIGH SPEED OR ULTRASONIC EQUIPMENT. Eg :VARICELLA ZOSTER ,CYTOMEGALOVIRUS ,RUBEOLA & MUMPS VIRUS ,RUBELLA VIRUS , MYCOBACTERIUM TUBERCULOSIS, CANDIDA ALBICANS. www.indiandentalacademy.com
  • 10. AREAS OF INFECTION CONTROL •INFECTION CONTROL IN THE CLINICAL AREA. •INFECTION CONTROL IN THE LABORATORY SET UP. www.indiandentalacademy.com
  • 11. INFECTION CONTROL IN CLINICAL AREA. •PERSONAL PROTECTION EQUIPMENTS(PPE). •ENVIRONMENTAL SURFACE CLEANING &DISINFECTION . •INSTRUMENT STERILIZATION. •DISPOSAL OF WASTE. www.indiandentalacademy.com
  • 12. PERSONNEL PROTECTION EQUIPMENT (PPE) •Protective clothing. •Gloves. •Masks. •Protective eyewear. www.indiandentalacademy.com
  • 13. CATEGORIES OF PERSONEL •CAT 1-personnel routinely performs tasks that involve exposure to blood or other potentially infectious materials. •CAT 2-are personnel who on occasion may perform tasks that involve exposure to blood and other potentially infectious materials. www.indiandentalacademy.com
  • 14. PROTECTIVE CLOTHING •Primary function- Protect worker from exposure to contaminated materials •Fluid resistant. •Minimal skin exposures,ie.long sleeves. •Cuff of the sleeve covered by the band of the •glove. •High risk procedures need have at least knee length when seated. •Buttons ,zippers,should be hidden and not exposed. www.indiandentalacademy.com
  • 15. GUIDE LINES •Protective clothing not to be worn outside the dental office. •Change at least daily. •Incase soiled, change immediately. •Remove while relaxing esp. in the cafeteria while eating or drinking. www.indiandentalacademy.com
  • 16. GLOVES  Gloves should be used while touching ---- 1. Blood and body fluids. 2. Mucous membrane. 3. Non intact skin of the patient. 4. Items or surfaces soiled with blood or body fluids. www.indiandentalacademy.com
  • 17. Types of gloves 1. 2. 3. 4. 5. Vinyl or latex sterile, single use surgical procedure. Vinyl or latex - non sterile, single use examination procedure. Rubber / plastic material - non sterile,multiple use - over gloving. Polyethylene - non-sterile,multiple use over gloving. Nylon glove – non sterile ,multiple use – using beneath gloves. www.indiandentalacademy.com
  • 19. General precautions to be taken while using gloves      Wear gloves for all dental procedures Discard gloves whenever they have been contaminated. Do not leave the clinic or walk around wearing gloves. Wash hands after removing gloves. Used needles should not be recapped. www.indiandentalacademy.com
  • 20. REPROCESSING OF GLOVES     Rinse your gloved hands thoroughly in a hypochlorite solution. Then in clear water to remove the disinfectant. Wash with soap and water and rinse thoroughly. Remove the gloves and hang them up by the cuffs to dry  Dust glove powder on the inside of the gloves .  Test for holes in the house before reuse.  Autoclave the gloves. www.indiandentalacademy.com
  • 21. MASKS    Surgical masks / chin length plastic face shields must be worn to protect the face. Should have at least 95% filtration efficiency for particles 3-5 micrometer in diameter. Should be changed for each patient since its efficiency decreases as it traps moisture during dental procedures. www.indiandentalacademy.com
  • 22. EYE PROTECTION  The eyes of a dental professional are particularly susceptible to physical & microbial injury by virtue of their limited vascularity and diminished immune capacities.  Eyes must be protected during operative procedures by spectacles. www.indiandentalacademy.com
  • 24. •First scrub hands with warm water. •Get soap under the nails and clean with brush. •Rinse hands with cold water. •Wipe hands with paper towel or dry with warm air. www.indiandentalacademy.com
  • 26. AGENTS OF HAND CLEANING •Substituted phenol preparations like chlorhexidine gluconate and parachlorometaxylenol (pcmx). •4% chlorhexidine & 3% PCMX are equally sufficient. •Both remain in the tissues in an active form for prolonged periods thus maintaining a residual activity for prolonged periods. www.indiandentalacademy.com
  • 27. Method of sterilization  Moist heat (autoclaving)  Dry heat  Chemicals (chemiclaving) (hot air oven) www.indiandentalacademy.com
  • 28. Moist heat •Moist heat denatures & coagulates the protein of microbes. •Better than dry heat because of its higher efficiency of penetration. •Due to latent heat of vaporization present in moist heat. www.indiandentalacademy.com
  • 29. TYPES OF AUTOCLAVES POROUS LOAD AUTOCLAVES : 1. Autocycled high pressure vacuum models  .  Air is evacuated from the metal chamber by vacuum suction.  1210 C , AT 20 lb pressure for 30 min.  Towels ,suture materials,cotton rolls, rubber gloves ,root canal instruments. www.indiandentalacademy.com
  • 30. SMALL BENCH TOP AUTOMATIC AUTOCLAVE  Work on the principle of downward displacement of air as a consequence of steam entering at the top of the chamber.  Temp of 136oc ,at 32 lb pressure for 5 min www.indiandentalacademy.com
  • 31. STERILIZATION CYCLE Temperature Time Pressure Unwrapped instruments 134oc 3 min 30 psi Wrapped instruments 1210c 15-20 min 15 psi www.indiandentalacademy.com
  • 32. DRY HEAT  Less effective than moist heat  Higher temperatures ,longer periods &longer heating up time required for sterilization (45 min to reach 160oc).  Should have a time clock on the door ,so items cannot be added or removed during the cycle & a fan to distribute the heat evenly. www.indiandentalacademy.com
  • 33. CHEMICAL STERILIZATION  Combination of formaldehyde,alcohol,acetone,ketone &steam at 20 psi serves as an effective sterilizing agent.  biocidal action of formaldehyde depends on its alkylation of microbial nucleic acids,which control protein synthesis.  Takes longer time than an autoclave (30 min)for packaged instruments (shorter than hot air oven) www.indiandentalacademy.com
  • 34. Advantage of chemiclave :  Shorter cycle  Lack of corrosion of instruments /burs.  Adequate ventilation must be provided in order to expel the residual fumes released on opening the chamber at the end of the cycle. www.indiandentalacademy.com
  • 35. Ethylene oxide gas sterilization.  A flammable ,explosive and toxic gas to which all types of microbes are susceptible.  Biocidal activity is due to alkylation and hence causes denaturation of microbial nucleic acid.  Biocidal activity increases in the presence of moisture.  Plastic ,metal,rubber or cloth can be sterilized without damage.  Equipment is costly & gas is toxic. www.indiandentalacademy.com
  • 36. STERILIZATION BY GAMMA IRRADIATION :  Used for needle,sutures ,gloves etc GLASS BEAD STERILIZATION :  Heating glass beads in a chamber into which instrument is inserted for 10-30 sec.  2100c –230 0c .  Suitable for very small instruments like www.indiandentalacademy.com R.C.T instruments ,burs ,pliers etc.
  • 37. Water boilers… •does not achieve sterilization as many spores can with stand it. •Cross infection from contaminated water containing bacterial spores not killing by boiling. www.indiandentalacademy.com
  • 38. Monitoring sterilization Three forms  physical monitoring.  Chemical monitoring.  Biological monitoring. www.indiandentalacademy.com
  • 39.  PHYSICAL MONITORING :Refers to periodical observation of displays or gauges on the sterilizer during a cycle to ensure the sterilization process. www.indiandentalacademy.com
  • 40. Chemical monitoring. 1. 2. Two types are available process indicators :- consist of colour changing material (liquid /paper) which changes color upon exposure to appropriate sterilization cycle. TST strips (TIME ,STEAM,TEMPERATURE) change color when all parameters have been adequately achieved in the sterilization cycle. www.indiandentalacademy.com
  • 41. BIOLOGICAL MONITORING.  Indicator used are heat resistant bacterial spores (bacillus stearothermophillus ,bacillus subtilis )  If the spores are killed ,then less resistant microbes are killed more readily and sterility is achieved. www.indiandentalacademy.com
  • 42. Classification of instruments to be sterilized  Critical  Semi critical  Non- critical www.indiandentalacademy.com
  • 43. Critical  Surgical other instruments used to penetrate soft tissue / bone.  Should be sterilized after each use. eg :-forceps ,scalpels,bone chisels,scaling instruments,surgical burs. www.indiandentalacademy.com
  • 44. Semi critical  Instrument that do not penetrate soft tissue / bone but contact oral tissues. eg :-mirrors ,plastic instruments,burs etc. www.indiandentalacademy.com
  • 45.  Non critical :Items which do not come into contact with body fluids. eg:-light cure tips,glass slab,cement spatula,orthodontic pliers,dapen dish. www.indiandentalacademy.com
  • 46. Procedure before sterilization •Pre soaking of instruments. •Pre sterilization cleaning • manual • ultrasonic www.indiandentalacademy.com
  • 47. Presoaking •Keeps instruments wet. •Prevents drying of saliva &blood on the instruments. •Facilitating easy cleaning. •solution used may be phenol or gluteraldehyde. www.indiandentalacademy.com
  • 48. Pre sterilization cleaning. 1. 2.     Manual cleaning Ultrasonic cleaning :Employ piezo-electric oscillators situated underneath S.S enclosures to create oscillations in a fluid filled tank. Oscillations are transformed into a series of high frequency sound waves, which cause intense microscopic cavitation in the fluid. Large number of these tiny bubbles collapse creating minute vacuum areas which are responsible for the scrubbing effect. 2 – 20 min www.indiandentalacademy.com
  • 49. ADVANTAGE OF ULTRASONIC CLEANING OVER MANUAL CLEANING •Increased efficacy. •Reduced danger of aerosolization. •Reduced incidence of instrument injuries. •Increased tarnish removal and cleanliness. •Reduction in manual labour. www.indiandentalacademy.com
  • 50. Sterilization trays Three types 1. Fully closed system.(with individually packed items in commercially available sterilization bags) 2. Perforated trays.(with fitted covers wrapped with sterilization paper) 3. Open tray system.(sealed with a see through sterilization bag) www.indiandentalacademy.com
  • 51. Cold sterilization    process of disinfecting instruments / equipment by using a liquid chemical germicide is called cold sterilization. Used for heat sensitive instruments. Aseptic rinsing with sterile water and drying should follow this disinfection process. www.indiandentalacademy.com
  • 52. Disinfectants used in dentistry     Glutaraldehydes. Chlorine compounds. Iodophors. Synthetic phenolics. www.indiandentalacademy.com
  • 53. Chemical disinfectants effective in inactivating HIV  SODIUM HYPOCHLORITE (0.1 -0.5%)  CHLORAMINE 2% (TOSYL CHLORAMIDE SODIUM)  ETHANOL 70%  2 –PROPANOL 70% (ISOPROPYL ALCOHOL)  PROVIDONE IODINE 2.5%  FORMALDEHYDE 4%  GLUTARAL 2% (GLUTARALDEHYDE)  HYDROGEN PEROXIDE 6% www.indiandentalacademy.com
  • 55. GLUTARALDEHYDE  20 min. immersion in a 2% alkaline glutaraldehyde solution - disinfection.  6 -10 hours immersion – sterilization. properties :-  high biocidal activity.  Broad antimicrobial spectrum within 10-30 min.  Sporicial after 7-10 hrs. of exposure at room temperature.  Noncorrosive.  Penetrates blood, pus & organic debris.  Induces severe tissue irritation upon prolonged contact.  Discolors nickel coated impression trays & carbon steel www.indiandentalacademy.com
  • 56. Quaternary ammonium compounds. Advantages : Bactericidal against gram positive bacteria.  Non –irritating.  Economical.  Pleasant odor. Disadvantages:-  inactivated by organic matter.  Can sometimes support gram negative bacteria.  Easily inactivated by presence of anionic detergents, soaps &hard water. www.indiandentalacademy.com
  • 57. Chlorine compounds Advantages : Rapid antimicrobial action.  Effective in dilute solution.  Economical  Sodium hypochlorite is useful as a broad spectrum bactericidal, virrucidal, tuberculocidal surface disinfectant. www.indiandentalacademy.com
  • 58. Disadvantage:•Sporicidal effects noted only at high concentration. •Prepared solution has only limited shelf life. •Activity diminished by presence of organic matter & altered pH  Unpleasant odor  Irritates skin &eyes.  Can degrade plastic & rubber coated instruments. www.indiandentalacademy.com
  • 59. Chlorine dioxide Advantages : Instrument and environmental surface disinfectant /sterilant  Rapid 3 min. disinfection ,6 hrs. sterilization.  Non-irritating and non-toxic. Disadvantage:-  Must be prepared daily  Does not readily penetrate organic debris.  Only 24 hrs shelf life. www.indiandentalacademy.com
  • 60. Iodophors Advantages:1. Broad spectrum disinfectant, especially effective against heavy viral contamination. 2. Biocidal activity occurs within 3-30 min. 3. Effective in dilute solution. Disadvantages:1. Not a sterilant. 2. Unstable at high temperature. 3. Must prepare daily. 4. Inactivated by hard water. 5. May discolor some light colored surfaces. www.indiandentalacademy.com
  • 61. Alcohols (70% isopropyl alcohol &70% ethyl alcohol) Advantages :1. Rapidly bactericidal against most gram positive & gram negative bacteria. 2. Active against many lipophilic viruses 3. Economical. Disadvantages :1. Ineffective against bacterial spores. 2. Diminished activity in organic matter and tissue debris. 3. Bactericidal activity diminished greatly. www.indiandentalacademy.com
  • 62. Synthetic phenols  They act as a protoplasmic poison which precipitate the protein and destroy the cell wall. Advantages:- 1. synergistic effect instead of additive. 2. Broad antimicrobial spectrum. 3. Can be used on metal, glass, rubber &plastic. 4. Less toxic & corrosive. 5. Economical. Disadvantages:1. Not a sterilant 2. No re-use life. 3. Irritates skin & eyes. www.indiandentalacademy.com
  • 63. Two methods of surface asepsis. • Cleaning & disinfecting the contaminated surface. • Preventing the surface from becoming contaminated. www.indiandentalacademy.com
  • 65. Surface cover. • Materials impervious to moisture. • On surfaces difficult to clean. • To be changed between patients. (impervious- backed paper, aluminium foil / plastic covers ) www.indiandentalacademy.com
  • 68. Spray – wipe spray technique. • Spray the surface. • Wipe in systematic pattern contacting each surface at least twice. • Spray again. • Allow solution to dry and then wipe in 10 minutes for proper disinfection. www.indiandentalacademy.com
  • 70. • The disinfectant used must be a hospital level disinfectant ie.it should inactivate the Polio 2 virus and Mycobacterium Tuberculosis . • Isopropyl alcohol and quaternary ammonium compounds are not recommended as they achieve less level of surface wettability compared to that of water based disinfectants. www.indiandentalacademy.com
  • 71. Disinfecting dental equipments. • Hand piece • 3 way syringe tips • HVE tips • aspirators www.indiandentalacademy.com
  • 72. Hand pieces • Most are autoclavable. • Depends on manufacturers guidelines. • Prior cleaning and lubrication is mandatory. • Hand piece is placed in autoclavable pouch with TST strips. www.indiandentalacademy.com
  • 73. Steps for proper sterilization of hand pieces. • Decontamination inside n outside. • Rinse . • Flush lines. • Dry . • Sterilize . • Lubricate and run hand piece. • Bag wrap. www.indiandentalacademy.com
  • 74. Suck –back devices / check valves on hand pieces  Suck –back devices prevent any residual water left in the line from the previous patient, from going into next patient’s operating field when the procedure starts.  Check valve is a simple gadget that will tell you immediately if any retained water is coming back out of the hand piece.  Both these devices can be fitted on to an older hand pieces. www.indiandentalacademy.com
  • 77. Three way syringe tips / high velocity evacuation tips / aspirators    3 –way syringe should be treated in the same manner as hand piece. HVE tips –metal tips are autoclavable. Plastic tips must be disposed off after single use. Aspirators –disinfectant flushes for the aspirators should be done after each patient. www.indiandentalacademy.com
  • 78. Sterilization & disinfection of individual articles. Disinfection of dental impressions :ALGINATE:-iodophores / glutaraldehyde – 15 min. LYSOL spray – 10 min. www.indiandentalacademy.com
  • 79. Burs ethylene oxide 4-12 hours autoclave. carbon steel instruments chemical vapour---20 min at 270 °f ethylene oxide ----4-12hours dry heat oven---60-120 min at 320°f tungsten carbide instruments chemical vapour---20 min at 270 °f dry heat oven---60-120 min at 320°f www.indiandentalacademy.com
  • 80. Corrosion of instruments. corrosion is an electrolytic process in which the contact of two dissimilar metals sets up a potential difference resulting in an electron flow.This flow leaves behind reactive ions that readily combines with atmospheric oxygen to form oxides (rust). Corrosion resistance of orthodontic grade steel is directly proportional to its carbon content and the chromium content ( PASSIVATION EFFECT) www.indiandentalacademy.com
  • 81. Sterilization in orthodontics. David Drake(1997)JCO    Plastic items & heat sterilizable cheek retractors – immerse in procide (strelalization solution whish turns milky after autoclaving) Hand pieces & photographic mirrors – sterilized in a kavo-klave Plier racks & instruments are placed in a wire basket & run through an ultrasonic cleaner containing rust inhibiting non-ionic multipurpose ultrasonic cleaner . www.indiandentalacademy.com
  • 82.      Ultra-sonic solution should be changed daily & covered during cleaning to reduce aerosols. Dried blood must be scrubbed off & repeat ultrasonic cleaning . Heavy duty nitril gloves are required for handling contaminated instruments. After cleaning instruments are dipped in a sodium nitrite rust inhibitor Auto clave for 20 min &20 min for cooling. www.indiandentalacademy.com
  • 83. STERILIZATION OF NiTi WIRES  Heat sterilization is the most reliable method - (Steam autoclaving at 1210C,15-20psi for 20 min)  Chemical sterilization are corrosive &attack metals immersed in them (2% acidic Glutaraldehyde) • STERILIZATION OF ORTHODONTIC BANDS:-15 SECONDS OF GLASS BEAD STERILIZATION.(SMITH et www.indiandentalacademy.com al 1986 AJO)
  • 84. CAUSES OF STERILIZATION FAILURE (GEORGE 1993 JCO)  CYCLE TIME TOO SHORT  TEMPERATURE TOO LOW  FAILURE TO PREHEAT  FAULTY STERILIZER  INTERRUPTING OF CYCLE  OVERLOADING OF CHAMBER  INADEQUATE STAFF TRAINING  IMPROPER PRECLEANING, PACKAGING  FAILURE TO USE BIOLOGICAL INDICATOR TESTING. www.indiandentalacademy.com
  • 85. Disposal of waste •Its should be disposed in tamper proof containers/ boxes. •Its should be labeled as BIOHAZARD. •Should be in tune with the existing laws of the area. •Sharp material should be stored in hard walled leak proof containers ,red in color. www.indiandentalacademy.com
  • 87. Color coding for waste disposal •Yellow --- waste for incineration . •Yellow with --- waste for land fill . black stripes •Light blue--- for autoclaving before disposal •Red ---human anatomical wastes. •Black ---normal household wastes. www.indiandentalacademy.com
  • 89. CONCLUSION PREVENTION IS BETTER THAN CURE www.indiandentalacademy.com
  • 90. Thank you For more details please visit www.indiandentalacademy.com www.indiandentalacademy.com