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DENTAL IMPLANTS
SANGEETA ROY
INTRODUCTION
• Dental Implant:- “Agraft or insert set firmly or deeply into
or onto the alveolar process that may be prepared for its
insertion"
HISTORY 1. First evidence in Incas &
Mayans(600 BC)
2. 2500 BC Egyptians nailed
Copper studs with seashells
(carving like teeth)
3. 1809-Maggiolo-Gold Implant
4. 1913 FIRST Implant system by
greenfield
5. 1939-Strock-Vitallium screw in
root form
6. 1943- Dahl- Intramucosal
implant (Button insert)
7. 1946- Goldberg & Gershkoff-
Subperiosteal Implant
8. 1964- Linkow- Blade implant
9. 1970- Roberts- Ramus implant
10. Per Ingvar Branemark- 1965- 1st
used pureTi implant
1982- osseointegration
proposed
11. 1988- National institute of
health recognized dental implant
subperiosteal
Blade
Ramus
INDICATION
1. Complete denture patient with
advanced residual ridge
resorption
2. Partially edentulous where RPD
is contraindicated (i.e. reduced
masticatory efficacy)
3. Single tooth replacement
CONTRAINDICATION
• Uncontrolled or controlled
diabetes/ medically
compromised
• Smoking
• Chronic steroid therapy.
• alcohol abuse
• High dose irradiation
• Pathologic conditions of the hard
and soft tissues
• Presence of untreated or
unsuccessfully treated
periodontal diseases.
ADVANTAGE 1. Preservation of bone
2. Improved function
3. Aesthetic
4. Stability & retention
5. Comfortable to patient
DISADVANTAGE
1. Expensive
2. Cant be used in medically
compromised patient
3. Longer duration of treatement
4. Anatomic limitation
RATIONALE 1. Loss of tooth cause atrophy of
surrounding bone, Dental
implant maintain the bone
levels by applying direct forces
on bone.
2. Allow the pt to use there
muscles of mastication, prevent
atrophy of muscles
3. Closest replacement of natural
teeth- boost self confidence
4. Becomes a part of body after
osseointegration
1. IMPLANT BODY( FIXURE)
PARTS OF
IMPLANT
Crest module
Body
Apex region
2. HEALING SCREW( COVER
SCREW): prevent growth of tissue
over implant edge.
given during first stage surgery
3. HEALING CAPS( GINGIVAL
FORMER): projected into oral
cavity, prevent overgrowth of tissue
given after healing in second stage
surgery
4. ABUTMENT: For retention of
prosthesis, resemble prepared
tooth.
may be: screw retention,
cement retention, to retain
Removable prosthesis
CLASSIFICATION
• DEPENDING ON PLACEMENT
WITHINTHETISSUE
1. Subperiosteal: receive primary
bone support resting on it
2. Transosteal: penetrate both
cortical plate & passes through
entire thickness of alveolar
bone
3. Endosteal: penetrate only one
cortical plate
Basal implant : if take support from
basal bone
Endosteal implant Root form( vertical )
Cylindrical : microscopic retention
Press fit form
Screw root form( threaded)
Combination
Plate form( horizontal)
Flat & narrow in facio-lingual direction
4. Ramus frame
5. Intramucosal
6. Endodontal
• DEPENDING ON SHAPE
1. Screw form
2. Bullet shaped
3. Basket form
4. Root form
5. Plates / blades
Bullet shaped
Basket shaped
Blade form
• DEPENDING ONTHE MATERIAL USED
1. Metallic & metallic alloy
2. Non metallic
3. Polymer
4. Composite
Titanium
Silver
Co-Cr-Mo
Fe- Cr- Ni
Ti- Al-VnCeramic HA
Al- oxide
Carbon
HA
Titanium
Ceramic Carbon
• DEPENDING ON REACTIONTO
BONE
1. Biotolerant : Polymers
2. Bioinert :Ti , Zirconia
3. Bioactive : Glass ceramic
• BASED ON MACROSCOPIC
BODY DESIGN
1. Hollow
2. Cylindrical
3. Vented
4. Threaded
• BASED ONTHE SURFACE
1. Machined surface
2. Textured surface (Acid etched )
3. Coated surface
• DEPENDING UPON
SURGICAL PROCEDURE
1. Single stage surgery procedure
2. Two stage surgery procedure
3. Direct single stage
• DEPENDING UPON
HISTOLOGICAL FEATURES
1. Osseo integration
2. Fibro-osseous integration
COMPONENTS
OF IMPLANT
DESIGN
• DIAMETER: ranging from 1.2-
2mm for mini implants upto 7
mm for wide diameter implants
 min 3.25 mm diameter is
required for strength
Most implants are of 4mm
diameter
• LENGTH: distance between
implant platform & apex
Commonly 8-13 mm
BASIC THREAD TERMINOLOGY
IMPLANT ABUTMENT
ATTACHMENT
SURFACE
MODIFICATION
• Passivation
• Ion implantation
• Surface texturing
BONE
CLASSIFICATION • MISCH’S CLASSIFICATION (based
on bone density)
• D1: dense cortical bone
• D2: thick dense to porous
cortical bone on the crest and
coarse trabecular bone within.
• D3: thin porous cortical bone on crest
and fine trabecular bone within.
• D4: fine trabecular bone
• D5: immature, non-mineralized bone.
• D1: > 1250 HU; D2: 850 to 1250 HU;
D3: 350 to 850 HU; D4: 150 to 350
HU; and D5: < 150 HU.
IMPLANT –
BONE
INTERFACE
• There are two basic
theories regarding the
bone-implant interface.
a)Fibro-osseous integration
b) Osseointegration
• Greek word osteon: bone,
and the Latin integrare : to
make whole.
FACTORS
AFFECTING
BONE
IMPLANT
INTERFACE
• Implant biocompatibility
• Implant surface/dimension
• Implant bed
• Loading condition
• Primary implant stability
• implant length and diameter.
• Surgical technique
• Bone quality and quantity
Implant
biocompatibility
• Materials used are:
• Cp titanium (commercially pure
titanium)
• Titanium alloy (titanium-
6aluminum-4vanadium)
• Zirconium
• Hydroxyapatite (HA), one type of
calcium phosphate ceramic
material
• Implant surface
• Pitch, is an important factor in implant
osseointegration.
• Increased depth between individual threads allows for
improved contact area between bone and implant.
• Moderately rough surfaces with 1.5µm also, improve
contact area between bone and implant surface.
• Reactive implant surface by anodizing (Oxide layer),
acid etching or HA coating enhanced osseointegration
• Implant bed
Primary
implant
stability
• micromotion of less than 30 μm
– no effect on osteointegration
• adequate‟ insertion torque
• the additional torque used to
secure or evaluate fixation of an
implant in
• bone (30-35Nw)
• But may actually result in
pressure necrosis and/or increase
the strain magnitude at the
interface and therefore increase
the amount of damage.
• implant length - > length better
successrate
• less than 10 mm – 50% failure
DISTANCE
BETWEEN
TWO
IMPLANTS
Surgical technique • 47°C at less than 1 minute to
avoid overheating the bone The
Heat generated is related to
• The presence and temperature
of irrigation
• Amount of bone being prepared
• Drill sharpness and design
• Time of preparation
• Depth of the osteotomy
• Pressure on the drill
• Drill speed
• Variation in cortical thickness.
Drill speed
• The speed of drills may be adjusted in relation to the quality of the bone being
prepared.
• D3 – 800 rpm
• D1- 2500 rpm proceed without exerting excessive pressure .
• Time of preparation
• pause approximately every 5 to 10 seconds.
• Pressure on the drill
• The average force placed on a hand piece during preparation of an osteotomy is
1. 2Kg. Enough pressure should be used to proceed at least 1 mm every 5
seconds
Bone quality
and
quantity
• The lower the modulus and the
less amount of bone–implant
contact will be there
• These factors are critically
important in relation to the
success or failure of
osseointegration
• Based on the above, there is a
general agreement among
clinicians that the mandibular
interforaminal area contains the
best qualitybone
OSSEOINTEGRATION
• Branemark in 1982 proposed that
implants integrate with bone
such that the bone is laid very
close to the implant material
without an intervening
connective tissue.
• Osseointegration is defined as “
the process and resultant
apparent direct connection of the
endogenous material surface &
the host bone tissues without
intervening connective tissue.”
• To obtain a successful osseointegration
Branemark and coworkers proposed
numerous factors.
• According to the proponents the oxide
layer should not be contaminated or
else inflammatory reaction follows
resulting in granulation tissue
formation.
• The temperature during drilling should
be controlled by copious irrigation, if
not can inhibit alkaline calcium synthesis
there by preventing osseointegration.
• The first month after fixture insertion is
the critical time period for initial healing
period.When loads are applied to the
fixture during this period primary
fixation is destroyed.
FIBRO-OSSEOUS
INTEGRATION
• CharlesWeiss, 1980’s stated that
fibroosseous ligament is formed
between the implant & the bone
& this is equivalent to PDL found
in gomphosis.
• Fibroosseous integration may
show initial success but failed to
show long term stability.
OSSEOINTEGRATION
VS BIO INTEGRATION • Meffert et al, (1987) redefined and
subdivided the term
osseointegration into “adaptive
osseointegration” and
“biointegration”.
• “Adaptive osseointegration” has
osseous tissue approximating the
surface of implant without apparen
soft tissue interface at the light
microscopic level.
• “Biointegration” is a direct
biochemical bone surface
attachment confirmed at the
electron microscopic level.
• Dr.charlesWeiss, stated that the collagen fibers invest the implant,
originating at the trabeculae of cancellous bone on one side,
weaving around the implant, and reinserting into a trabeculae on the
other side
• no real evidence to suggest that these fibers functioned in the mode
of periodontal ligament.
• the forces applied resulted in widening fibrous encapsulation,
inflammatory reactions, and gradual bone resorption there by
leading to failure.
Immediate
loading
• Implantplacement with primary
stabilityand prosthetic loading
with a provisional prosthetic
tooth at the same clinical visit or
With in 2 wks
Early
loading
• Implants placed with primary
stability and loaded with a
provisional prosthesis at a
subsequent clinical visit .
• should follow the onset of
osteogenesis since bone
formation is enhanced by
mechanical stimulation.
Therefore, early loading should
occur only after approximately 3
weeks of healing
Conventional
loading
• Implant placement (typically
achieving primary stability) and
healing for 3 to 6 months in a
submerged or non-submerged
mucosal orientation.
• This time frame reflects the
requirement for osteogenesis
and woven bone remodelling to
load-bearing lamellar bone and
acknowledges the original
recommendations of Brånemark
.
DIAGNOSIS
• Clinical examination of the
jawbone consists of palpation and
probing through the soft tissue
(intra oral bone mapping) to
assess the thickness of the soft
tissue at the proposed surgical
site.
CLINICAL
RADIOGRAPHICAL
Radiographic
analysis
• Types of imaging modalities:
• Periapical radiograph
• Occlusal
• OPG
• Cephalometric
• CT – 3 dimentional
• CBCT
• Phase 1:
• Pre surgical imaging:
• Identify disease
• Determine bone quality and quantity
• Determine implant position and orientation
• Phase 2:
• Surgical and intra operative imaging:
• Focused on assisting in surgical and prosthetic
intervention in pt
• Phase 3:
• Post prosthetic implant imaging –
• to evaluate long term maintenance of implant
and function
IMPORTANCE OF BONE
DENSITY
Type advantage disadvantage
D1
Anterior mandible
, 5 months healing time
dense lamellar bone with
complete haversian
systems
Less stresses -near crest
More BIC
fewer blood vessels
slower rate of 0.6 um /day
more difficult to prepare
Bone is easily overheated
D2-anterior mandible, followed by
the posterior mandible. Occasionally
ant .maxilla
bone healing within 4 month
bone provides excellent
BIC
intrabony blood supply –
reduce overheating
Improve primary stability
due to apical engage
Stress - around the crest greater
magnitude
D3- ant- maxilla post.either arch
TPS/HA
Maximum use of bone width
May need sinus grafting,additional
implant
Minimal osteotomy
Good blood supply
the stripping of the thin facial plates
during the osteotomy
More delecate to manage
less than 1500 rpm
<50% BIC
6month healing
D4-posterior maxilla
Need bone grafting
Maximum use of bone length
little or no cortical crestal bone
<25% BIC
to 8 months of undisturbed healing
IMPLANT SITE
PREPARATION
• Alveolar ridge reconstruction with
preprosthetic surgery
• Alveolarbone preservation
following tooth extraction
(immediate implants, GBR,
osseous grafting etc.)
• Sinus lift/ grafting procedures
• Alveolar ridge augmentation
• Implant site development using
ridge splitting technique
• Alveolar ridge development using
distraction osteogenesis
• Growth factors for implant site
development
TREATMENT
PLANNING 1 .prosthesis design
2. patient force factors
3. Bone density/availability in
edentulous site
4. Key implant position and number
5 .Implant size
6.Implant design
• PROSTHESIS DESIGN: Implant supported denture , ovrer denture,
fixed denture
• PATIENT FORCE FACTORS: parafunctional habit (bruxism,
clenching)
• the force applied to the restoration differs by magnitude ,
duration, type and pre disposing factor may need
1) additional implants that are wider in diameter
2)proper incisal guidance
3) narrow posterior occlusal table
4)enameloplasty of opposite natural teeth.
• CROWN HEIGHT SPACE- should be between 8-12mm when not
in range-
1) shorten cantilever length
2 )Increase number and diameter of implant and splint them
3) Fabricate removable restoration that incorporate soft tissue
support Remove them at night
• BONE DENSITY- softer bone Increase number and diameter of
implant with more and deeper threads. As more stress over crest
so implant diameter is more significant then length.
• Minimum bone height for initial fixation & loading in
• D1=7mm, D2=9mm,D3=12mm, D4->12mmm
IMPLANT
POSITION
• Ideally occlusal force should be
directed through the long axis of
the implants.Therefore ,the
angle of the osseous ridge crest
is a key determinant of implant
angulation
• Maxilla anterior – 12 degree
• Mandible premolar - 10-15
degree
• Molar – 20-25 degree
SURGICAL
PROCEDURE
• Implant site evaluation:
• Minimum bucco –lingual
width– 7mm
• Mesio –distal 6.5mm
• Height – 11mm
• Soft tissue reflection – mid
crestal incision with a margin
of 1.5mm keratinized tissue
buccally extending to the sulcus
of adjacent teeth
• Implant osteotomy:
• Start with 2mm end cutting drill at the center of crest with 2500
rpm and copious irrrigtion upto 7-9mm
• Assess for proper position ,If incorrect position then side cutting
drill is used to stretch the osteotomy site.
• IOPA ensure the proper position with measuring tool
• Osteotomy proceeds with increasing size of twist drill bit shorter
than the size of desired implant
• Final implant position should clear the adjacent tooth and the
outer crestal cortical plate by 1.5mm.
• Implant placement:
• After final osteotomy, the site is lavaged and aspirated to
remove debris and blood
• The implant is rotated with 30 rpm (not more than 35 rpm) by
low speed high torque hand piece /hand ratchet
• The implant should inserted slightly above (one stage) or
below (Two stage). It should be rigid with no mobility on slight
compression
• Post insertion radiograph should be made to evaluate the
position , adjacent vital structure, crest module position.Any
correction can be made at this time. Low profile cover screw
is inserted into the implant body. Flaps most often
approximated with 4-0 suture material.
• If implant position is not within the ideal range, it may be
removed and reinserted.
IMPLANT
MAINTENANCE
• The principle is to detect peri implant
infections as early as possible
• The basis is a regular recall and repeated
assessment of the following key
parameters around each implant.
• Check the presence of-
 plaque
 bleeding tendency of the peri implant
tissue
 Suppuration
 Presence of peri implant pockets
 Radiological evidence of bone loss.
• If plaque and /or an increased tendency to bleed are detected
 implants are mechanically cleaned using a rubber cup and
polishing paste.
 Oral hygiene practices should be checked, and the proper plaque
control technique should be instructed and reinforced
• In the presence of pus or if first signs of peri-implant
tissue destruction are detected (pockets 4-5 mm &
slight bone loss)
 Oral hygiene practices combined with application of a
local antiseptic.
 The periimplant pockets are irrigated with 0.2%
Chlorhexidene and the patient is advised to rinse twice
daily with 0.12%Chlorhexidene.
• If pocket depth > 5mm, radiograph is taken.
If there is clear evidence of bone loss:
 then a microbiological sample is taken.
 If evidence of anaerobic flora found:
 Oral hygiene practices combined with application of a local
antiseptic & systemic antimicrobial therapy
• If the bone destruction is advanced:
 surgical intervention to correct the tissue morphology & GBR
techniques may be necessary
COMPLICATIONS • Inferior alveolar nerve injury
• Incision line opening
• Implant exposure: Partial/
complete
• Implant failure:
• Mobility of implant during healing
period
• Pain , infection
• Radiolucency around implant
whatever the cause, the implant
should be removed. Grafting and
reinsertion can be done after 8-
10wks.
CONCLUSION
• Dental implants have overall had high success rates, but their
placement and restoration still have the boundaries of both
biomedical science and art.
• The effectiveness of different designs of implant-supported
prostheses as well as associated treatment modalities,
prostheses retention and stability, leads to improvement in
speech, function and quality of life trials

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Implant

  • 2. INTRODUCTION • Dental Implant:- “Agraft or insert set firmly or deeply into or onto the alveolar process that may be prepared for its insertion"
  • 3. HISTORY 1. First evidence in Incas & Mayans(600 BC) 2. 2500 BC Egyptians nailed Copper studs with seashells (carving like teeth) 3. 1809-Maggiolo-Gold Implant 4. 1913 FIRST Implant system by greenfield 5. 1939-Strock-Vitallium screw in root form 6. 1943- Dahl- Intramucosal implant (Button insert)
  • 4. 7. 1946- Goldberg & Gershkoff- Subperiosteal Implant 8. 1964- Linkow- Blade implant 9. 1970- Roberts- Ramus implant 10. Per Ingvar Branemark- 1965- 1st used pureTi implant 1982- osseointegration proposed 11. 1988- National institute of health recognized dental implant subperiosteal Blade Ramus
  • 5. INDICATION 1. Complete denture patient with advanced residual ridge resorption 2. Partially edentulous where RPD is contraindicated (i.e. reduced masticatory efficacy) 3. Single tooth replacement
  • 6. CONTRAINDICATION • Uncontrolled or controlled diabetes/ medically compromised • Smoking • Chronic steroid therapy. • alcohol abuse • High dose irradiation • Pathologic conditions of the hard and soft tissues • Presence of untreated or unsuccessfully treated periodontal diseases.
  • 7. ADVANTAGE 1. Preservation of bone 2. Improved function 3. Aesthetic 4. Stability & retention 5. Comfortable to patient
  • 8. DISADVANTAGE 1. Expensive 2. Cant be used in medically compromised patient 3. Longer duration of treatement 4. Anatomic limitation
  • 9. RATIONALE 1. Loss of tooth cause atrophy of surrounding bone, Dental implant maintain the bone levels by applying direct forces on bone. 2. Allow the pt to use there muscles of mastication, prevent atrophy of muscles 3. Closest replacement of natural teeth- boost self confidence 4. Becomes a part of body after osseointegration
  • 10. 1. IMPLANT BODY( FIXURE) PARTS OF IMPLANT Crest module Body Apex region
  • 11. 2. HEALING SCREW( COVER SCREW): prevent growth of tissue over implant edge. given during first stage surgery 3. HEALING CAPS( GINGIVAL FORMER): projected into oral cavity, prevent overgrowth of tissue given after healing in second stage surgery
  • 12. 4. ABUTMENT: For retention of prosthesis, resemble prepared tooth. may be: screw retention, cement retention, to retain Removable prosthesis
  • 13. CLASSIFICATION • DEPENDING ON PLACEMENT WITHINTHETISSUE 1. Subperiosteal: receive primary bone support resting on it 2. Transosteal: penetrate both cortical plate & passes through entire thickness of alveolar bone 3. Endosteal: penetrate only one cortical plate Basal implant : if take support from basal bone
  • 14. Endosteal implant Root form( vertical ) Cylindrical : microscopic retention Press fit form Screw root form( threaded) Combination Plate form( horizontal) Flat & narrow in facio-lingual direction
  • 15. 4. Ramus frame 5. Intramucosal 6. Endodontal
  • 16. • DEPENDING ON SHAPE 1. Screw form 2. Bullet shaped 3. Basket form 4. Root form 5. Plates / blades Bullet shaped Basket shaped Blade form
  • 17. • DEPENDING ONTHE MATERIAL USED 1. Metallic & metallic alloy 2. Non metallic 3. Polymer 4. Composite Titanium Silver Co-Cr-Mo Fe- Cr- Ni Ti- Al-VnCeramic HA Al- oxide Carbon HA Titanium Ceramic Carbon
  • 18. • DEPENDING ON REACTIONTO BONE 1. Biotolerant : Polymers 2. Bioinert :Ti , Zirconia 3. Bioactive : Glass ceramic
  • 19. • BASED ON MACROSCOPIC BODY DESIGN 1. Hollow 2. Cylindrical 3. Vented 4. Threaded
  • 20. • BASED ONTHE SURFACE 1. Machined surface 2. Textured surface (Acid etched ) 3. Coated surface
  • 21. • DEPENDING UPON SURGICAL PROCEDURE 1. Single stage surgery procedure 2. Two stage surgery procedure 3. Direct single stage
  • 22. • DEPENDING UPON HISTOLOGICAL FEATURES 1. Osseo integration 2. Fibro-osseous integration
  • 23. COMPONENTS OF IMPLANT DESIGN • DIAMETER: ranging from 1.2- 2mm for mini implants upto 7 mm for wide diameter implants  min 3.25 mm diameter is required for strength Most implants are of 4mm diameter • LENGTH: distance between implant platform & apex Commonly 8-13 mm
  • 24.
  • 27. SURFACE MODIFICATION • Passivation • Ion implantation • Surface texturing
  • 28. BONE CLASSIFICATION • MISCH’S CLASSIFICATION (based on bone density) • D1: dense cortical bone • D2: thick dense to porous cortical bone on the crest and coarse trabecular bone within. • D3: thin porous cortical bone on crest and fine trabecular bone within. • D4: fine trabecular bone • D5: immature, non-mineralized bone. • D1: > 1250 HU; D2: 850 to 1250 HU; D3: 350 to 850 HU; D4: 150 to 350 HU; and D5: < 150 HU.
  • 29. IMPLANT – BONE INTERFACE • There are two basic theories regarding the bone-implant interface. a)Fibro-osseous integration b) Osseointegration • Greek word osteon: bone, and the Latin integrare : to make whole.
  • 30. FACTORS AFFECTING BONE IMPLANT INTERFACE • Implant biocompatibility • Implant surface/dimension • Implant bed • Loading condition • Primary implant stability • implant length and diameter. • Surgical technique • Bone quality and quantity
  • 31. Implant biocompatibility • Materials used are: • Cp titanium (commercially pure titanium) • Titanium alloy (titanium- 6aluminum-4vanadium) • Zirconium • Hydroxyapatite (HA), one type of calcium phosphate ceramic material
  • 32. • Implant surface • Pitch, is an important factor in implant osseointegration. • Increased depth between individual threads allows for improved contact area between bone and implant. • Moderately rough surfaces with 1.5µm also, improve contact area between bone and implant surface. • Reactive implant surface by anodizing (Oxide layer), acid etching or HA coating enhanced osseointegration • Implant bed
  • 33. Primary implant stability • micromotion of less than 30 μm – no effect on osteointegration • adequate‟ insertion torque • the additional torque used to secure or evaluate fixation of an implant in • bone (30-35Nw) • But may actually result in pressure necrosis and/or increase the strain magnitude at the interface and therefore increase the amount of damage. • implant length - > length better successrate • less than 10 mm – 50% failure
  • 34.
  • 35.
  • 37. Surgical technique • 47°C at less than 1 minute to avoid overheating the bone The Heat generated is related to • The presence and temperature of irrigation • Amount of bone being prepared • Drill sharpness and design • Time of preparation • Depth of the osteotomy • Pressure on the drill • Drill speed • Variation in cortical thickness.
  • 38. Drill speed • The speed of drills may be adjusted in relation to the quality of the bone being prepared. • D3 – 800 rpm • D1- 2500 rpm proceed without exerting excessive pressure . • Time of preparation • pause approximately every 5 to 10 seconds. • Pressure on the drill • The average force placed on a hand piece during preparation of an osteotomy is 1. 2Kg. Enough pressure should be used to proceed at least 1 mm every 5 seconds
  • 39. Bone quality and quantity • The lower the modulus and the less amount of bone–implant contact will be there • These factors are critically important in relation to the success or failure of osseointegration • Based on the above, there is a general agreement among clinicians that the mandibular interforaminal area contains the best qualitybone
  • 40. OSSEOINTEGRATION • Branemark in 1982 proposed that implants integrate with bone such that the bone is laid very close to the implant material without an intervening connective tissue. • Osseointegration is defined as “ the process and resultant apparent direct connection of the endogenous material surface & the host bone tissues without intervening connective tissue.”
  • 41.
  • 42. • To obtain a successful osseointegration Branemark and coworkers proposed numerous factors. • According to the proponents the oxide layer should not be contaminated or else inflammatory reaction follows resulting in granulation tissue formation. • The temperature during drilling should be controlled by copious irrigation, if not can inhibit alkaline calcium synthesis there by preventing osseointegration. • The first month after fixture insertion is the critical time period for initial healing period.When loads are applied to the fixture during this period primary fixation is destroyed.
  • 43. FIBRO-OSSEOUS INTEGRATION • CharlesWeiss, 1980’s stated that fibroosseous ligament is formed between the implant & the bone & this is equivalent to PDL found in gomphosis. • Fibroosseous integration may show initial success but failed to show long term stability.
  • 44. OSSEOINTEGRATION VS BIO INTEGRATION • Meffert et al, (1987) redefined and subdivided the term osseointegration into “adaptive osseointegration” and “biointegration”. • “Adaptive osseointegration” has osseous tissue approximating the surface of implant without apparen soft tissue interface at the light microscopic level. • “Biointegration” is a direct biochemical bone surface attachment confirmed at the electron microscopic level.
  • 45. • Dr.charlesWeiss, stated that the collagen fibers invest the implant, originating at the trabeculae of cancellous bone on one side, weaving around the implant, and reinserting into a trabeculae on the other side • no real evidence to suggest that these fibers functioned in the mode of periodontal ligament. • the forces applied resulted in widening fibrous encapsulation, inflammatory reactions, and gradual bone resorption there by leading to failure.
  • 46. Immediate loading • Implantplacement with primary stabilityand prosthetic loading with a provisional prosthetic tooth at the same clinical visit or With in 2 wks
  • 47. Early loading • Implants placed with primary stability and loaded with a provisional prosthesis at a subsequent clinical visit . • should follow the onset of osteogenesis since bone formation is enhanced by mechanical stimulation. Therefore, early loading should occur only after approximately 3 weeks of healing
  • 48. Conventional loading • Implant placement (typically achieving primary stability) and healing for 3 to 6 months in a submerged or non-submerged mucosal orientation. • This time frame reflects the requirement for osteogenesis and woven bone remodelling to load-bearing lamellar bone and acknowledges the original recommendations of Brånemark .
  • 49. DIAGNOSIS • Clinical examination of the jawbone consists of palpation and probing through the soft tissue (intra oral bone mapping) to assess the thickness of the soft tissue at the proposed surgical site. CLINICAL RADIOGRAPHICAL
  • 50. Radiographic analysis • Types of imaging modalities: • Periapical radiograph • Occlusal • OPG • Cephalometric • CT – 3 dimentional • CBCT
  • 51. • Phase 1: • Pre surgical imaging: • Identify disease • Determine bone quality and quantity • Determine implant position and orientation • Phase 2: • Surgical and intra operative imaging: • Focused on assisting in surgical and prosthetic intervention in pt • Phase 3: • Post prosthetic implant imaging – • to evaluate long term maintenance of implant and function
  • 53. Type advantage disadvantage D1 Anterior mandible , 5 months healing time dense lamellar bone with complete haversian systems Less stresses -near crest More BIC fewer blood vessels slower rate of 0.6 um /day more difficult to prepare Bone is easily overheated D2-anterior mandible, followed by the posterior mandible. Occasionally ant .maxilla bone healing within 4 month bone provides excellent BIC intrabony blood supply – reduce overheating Improve primary stability due to apical engage Stress - around the crest greater magnitude D3- ant- maxilla post.either arch TPS/HA Maximum use of bone width May need sinus grafting,additional implant Minimal osteotomy Good blood supply the stripping of the thin facial plates during the osteotomy More delecate to manage less than 1500 rpm <50% BIC 6month healing D4-posterior maxilla Need bone grafting Maximum use of bone length little or no cortical crestal bone <25% BIC to 8 months of undisturbed healing
  • 54. IMPLANT SITE PREPARATION • Alveolar ridge reconstruction with preprosthetic surgery • Alveolarbone preservation following tooth extraction (immediate implants, GBR, osseous grafting etc.) • Sinus lift/ grafting procedures • Alveolar ridge augmentation • Implant site development using ridge splitting technique • Alveolar ridge development using distraction osteogenesis • Growth factors for implant site development
  • 55.
  • 56. TREATMENT PLANNING 1 .prosthesis design 2. patient force factors 3. Bone density/availability in edentulous site 4. Key implant position and number 5 .Implant size 6.Implant design
  • 57. • PROSTHESIS DESIGN: Implant supported denture , ovrer denture, fixed denture • PATIENT FORCE FACTORS: parafunctional habit (bruxism, clenching) • the force applied to the restoration differs by magnitude , duration, type and pre disposing factor may need 1) additional implants that are wider in diameter 2)proper incisal guidance 3) narrow posterior occlusal table 4)enameloplasty of opposite natural teeth.
  • 58. • CROWN HEIGHT SPACE- should be between 8-12mm when not in range- 1) shorten cantilever length 2 )Increase number and diameter of implant and splint them 3) Fabricate removable restoration that incorporate soft tissue support Remove them at night • BONE DENSITY- softer bone Increase number and diameter of implant with more and deeper threads. As more stress over crest so implant diameter is more significant then length. • Minimum bone height for initial fixation & loading in • D1=7mm, D2=9mm,D3=12mm, D4->12mmm
  • 59. IMPLANT POSITION • Ideally occlusal force should be directed through the long axis of the implants.Therefore ,the angle of the osseous ridge crest is a key determinant of implant angulation • Maxilla anterior – 12 degree • Mandible premolar - 10-15 degree • Molar – 20-25 degree
  • 60. SURGICAL PROCEDURE • Implant site evaluation: • Minimum bucco –lingual width– 7mm • Mesio –distal 6.5mm • Height – 11mm • Soft tissue reflection – mid crestal incision with a margin of 1.5mm keratinized tissue buccally extending to the sulcus of adjacent teeth
  • 61. • Implant osteotomy: • Start with 2mm end cutting drill at the center of crest with 2500 rpm and copious irrrigtion upto 7-9mm • Assess for proper position ,If incorrect position then side cutting drill is used to stretch the osteotomy site. • IOPA ensure the proper position with measuring tool • Osteotomy proceeds with increasing size of twist drill bit shorter than the size of desired implant • Final implant position should clear the adjacent tooth and the outer crestal cortical plate by 1.5mm.
  • 62. • Implant placement: • After final osteotomy, the site is lavaged and aspirated to remove debris and blood • The implant is rotated with 30 rpm (not more than 35 rpm) by low speed high torque hand piece /hand ratchet • The implant should inserted slightly above (one stage) or below (Two stage). It should be rigid with no mobility on slight compression
  • 63. • Post insertion radiograph should be made to evaluate the position , adjacent vital structure, crest module position.Any correction can be made at this time. Low profile cover screw is inserted into the implant body. Flaps most often approximated with 4-0 suture material. • If implant position is not within the ideal range, it may be removed and reinserted.
  • 64. IMPLANT MAINTENANCE • The principle is to detect peri implant infections as early as possible • The basis is a regular recall and repeated assessment of the following key parameters around each implant. • Check the presence of-  plaque  bleeding tendency of the peri implant tissue  Suppuration  Presence of peri implant pockets  Radiological evidence of bone loss.
  • 65. • If plaque and /or an increased tendency to bleed are detected  implants are mechanically cleaned using a rubber cup and polishing paste.  Oral hygiene practices should be checked, and the proper plaque control technique should be instructed and reinforced
  • 66. • In the presence of pus or if first signs of peri-implant tissue destruction are detected (pockets 4-5 mm & slight bone loss)  Oral hygiene practices combined with application of a local antiseptic.  The periimplant pockets are irrigated with 0.2% Chlorhexidene and the patient is advised to rinse twice daily with 0.12%Chlorhexidene.
  • 67. • If pocket depth > 5mm, radiograph is taken. If there is clear evidence of bone loss:  then a microbiological sample is taken.  If evidence of anaerobic flora found:  Oral hygiene practices combined with application of a local antiseptic & systemic antimicrobial therapy • If the bone destruction is advanced:  surgical intervention to correct the tissue morphology & GBR techniques may be necessary
  • 68. COMPLICATIONS • Inferior alveolar nerve injury • Incision line opening • Implant exposure: Partial/ complete • Implant failure: • Mobility of implant during healing period • Pain , infection • Radiolucency around implant whatever the cause, the implant should be removed. Grafting and reinsertion can be done after 8- 10wks.
  • 69. CONCLUSION • Dental implants have overall had high success rates, but their placement and restoration still have the boundaries of both biomedical science and art. • The effectiveness of different designs of implant-supported prostheses as well as associated treatment modalities, prostheses retention and stability, leads to improvement in speech, function and quality of life trials