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OSSEOINTEGRATION - PART I
Dr Heenal Adhyaru
Seminar No: 14
CONTENT
 INTRODUCTION
 DEFINITIONS
 BONE PHYSIOLOGY
 TISSUE RESPONSE
 MECHANISM OF OSSEOINTEGRATION
 FACTORS AFFECTING OSSEOINTEGRAION
 BIOMATERIALS
 DESIGN CHARATERITICS
 IMPLANT SURFACE
 BONE DENSITY
 SURGICAL TECHNIQUE
 EVALUTION OF OSSEOINTEGRATION
 CONCLUSION
2
INTRODUCTION
 Per-Ingvar Branemark in 1964
 Dental implants for replacement of missing teeth.
 Comparison with direct fracture healing.
3
DEFINITION
 “Direct structural and functional connection between
ordered, living bone and surface of a load carrying implant”
by Branemark et al. in 1977 .
 “Functional ankylosis” by Schroeder et al. in 1981.
 “A biomechanical phenomenon whereby clinically
asymptomatic rigid fixation of the implant is achieved and
maintained in bone during functional loading.” by
Albrektson and Johansson in 2001.
4
BONE PHYSIOLOGY
5
6
Bone
Cells
Osteoblasts
Osteoclasts
osteocytes
Intercellular
substances
Inorganic
substances:
Bone mineral
Organic
substances :
Osteiod
7
8
S
9
TISSUE RESPONSE
 Biological response to the host tissue following the
placement of the implant:
1. Cellular injury
2. Inflammation and Coagulation
3. Repair and Regeneration
10
CELLULAR INJURY
injury: oxygen deprivation
reversible injury: cellular swelling
irreversible injury: point of no return
11
Najjar T. FONSECA: oral and maxillofacial surgery. Reconstructive and Implant
surgery
12
Najjar T. FONSECA: oral and maxillofacial surgery. Reconstructive and Implant
surgery
 Injured mesenchymal cells at the surgical site are not
conductive for osseointegration of the implant.
 The aim is to reduce ischemia and anoxia to a minimal
degree and for a very short duration during the surgical
phase of implant placement.
13
Najjar T. FONSECA: oral and maxillofacial surgery. Reconstructive and Implant
surgery
INFLAMMATION AND COAGULATION
14
15
 The micro-thrombin that are formed immediately after
surgery at the implant bone interface constitute the
framework for osseointegration to take place.
16
Najjar T. FONSECA: oral and maxillofacial surgery. Reconstructive and Implant
surgery
REPAIR AND REGENERATION
Branemark PI. Tissue-integrated prosthesis: osseointegration in clinical
dentistry Chicago: Quintessence Publishing Co.; 1985.
17
 Bone may react in three different ways as a response to the
necrosis
 Conditions for bone repair at an implant site depend on the
presence of:
1. Adequate cells
2. Adequate nutrition to these cells
3. Adequate stimulus for bone repair
18
Branemark PI. Tissue-integrated prosthesis: osseointegration in clinical
dentistry Chicago: Quintessence Publishing Co.; 1985.
ADEQUATE CELLS
 Osteoclasts Creeping substitution Osteoblasts
 Osteoclasts propagates at a rate of 50ɥm per day
 Undifferentiated mesenchymal cells
19
Branemark PI. Tissue-integrated prosthesis: osseointegration in clinical
dentistry Chicago: Quintessence Publishing Co.; 1985.
ADEQUATE BONE CELL NUTRITION
 Diffusion mechanism/ Angiogenesis
 Cancellous bone: 100ɥm
 Maximal vascular penetration rate:
 Cancellous bone: 0.5mm/ day
 Cortical bone: 0.05mm/ day
20
Branemark PI. Tissue-integrated prosthesis: osseointegration in clinical
dentistry Chicago: Quintessence Publishing Co.; 1985.
ADEQUATE STIMULUS FOR BONE REPAIR
21
Branemark PI. Tissue-integrated prosthesis: osseointegration in clinical
dentistry Chicago: Quintessence Publishing Co.; 1985.
STAGES OF OSSEOINTEGRATION
1. Incorporation by woven bone formation
2. Adaptation of bone mass to load (lamellar and parallel
fibered bone deposition)
3. Adaptation of bone mass structure to load (bone
remodeling)
22
Schenk RK. Osseointegration: a reality. Periodontology 2000. 1998; 17: p. 22-
35.
WOVEN BONE FORMATION
 The first bone tissue formed is woven bone. It is
characterized by a random, felt-like orientation of its
collagen fibrils, numerous, irregularly shaped osteocytes
and, at the beginning, a relatively low mineral density
 It grows by forming a scaffold of rods and plates and
thus is able to spread out into the surrounding tissue at a
relatively rapid rate.
 Woven bone formation clearly dominates the scene within
the first 4 to 6 weeks after surgery.
23
Schenk RK. Osseointegration: a reality. Periodontology 2000. 1998; 17: p. 22-
35.
LAMELLAR AND PARALLEL FIBERED BONE
DEPOSITION
Lamellar bone deposition Parallel fibered bone
deposition
24
 The linear apposition rate:
 1-1.5 ɥm/day  3-5 times larger than lamellar
bone
Schenk RK. Osseointegration: a reality. Periodontology 2000. 1998; 17: p. 22-
35.
 Both types of bone grow by apposition on a preformed solid
base.
 Three surfaces are qualified as a solid base for deposition of
parallel- fibered and lamellar bone:
 Woven bone formed in the first period of osseointegration
 Pre-existing or pristine bone surface
 The implant surface.
25
Schenk RK. Osseointegration: a reality. Periodontology 2000. 1998; 17: p. 22-
35.
BONE REMODELING
 It starts around the third month and after several weeks of
increasingly high activity, slow down again, but continues for
the rest of life.
 In cortical, as well as in cancellous bone, remodeling occurs
in discrete units, often called a bone multicellular unit, as
proposed by Frost.
 Remodeling starts with osteoclastic resorption, followed by
lamellar bone deposition.
26
Schenk RK. Osseointegration: a reality. Periodontology 2000. 1998; 17: p. 22-
35.
 Remodeling in the third stage of osseointegration
contributes; to an adaptation of bone structure to load in two
ways:
 It improves bone quality by replacing pre-existing, necrotic bone
and/or initially formed more primitive woven bone with mature, viable
lamellar bone.
 It leads to a functional adaptation of the bone structure to load by
changing the dimension and orientation of the supporting elements.
 Continuous replacement of old bone by new bone prevents
accumulation of micro-damage and fatigue as one possible
cause of aseptic implant loosening.
27
Schenk RK. Osseointegration: a reality. Periodontology 2000. 1998; 17: p. 22-
35.
MECHANISM OF INTEGRATION
OSBORN AND NEWESLEY – 1980
Distance osteogenesis Contact osteogenesis
28
Davies J. Mechanisms of Endosseous Integration. The International Journal of
Prosthodontics. 1998; 11(5): p. 391-401.
MECHANISM OF INTEGRATION
DAVIES - 1998
 Contact osteogenesis:
 Osteoconduction
 De novo bone formation
 Bone remodeling at discrete sites
29
Davies J. Mechanisms of Endosseous Integration. The International Journal of
Prosthodontics. 1998; 11(5): p. 391-401.
OSTEOCONDUCTION
30
Davies J. Mechanisms of Endosseous Integration. The International Journal of
Prosthodontics. 1998; 11(5): p. 391-401.
 Osborn (1979)categorized this bio-response into
the following three groups:
 Biotolerant type: characterized by distance
osteogenesis, the implant is not rejected from the
tissue, but it is surrounded by a fibrous connective
tissue
 Bioinert type: characterized by contact
osteogenesis, the osteogenic cells migrate directly to
the surface where they will establish de novo bone
formation, and
 Bioreactive type: the implant allows new bone
formation around itself, thereby exchanging ions to
create a chemical bond with the bone.
31
Davies J. Mechanisms of Endosseous Integration. The International Journal of
Prosthodontics. 1998; 11(5): p. 391-401.
DE NOVO BONE FORMATION
32
Secretion of two collagenous
proteins: osteopontin and
bone sialoprotein
Calcium phosphate
nucleation at the calcium
binding sites of one or more
of this protein.
Crystal growth phase
Collagen production and
subsequent collagen
mineralization
Davies J. Mechanisms of Endosseous Integration. The International Journal of
Prosthodontics. 1998; 11(5): p. 391-401.
 Initial protein layer with arginine-glycine-aspartic acid motif
adhesion. (Fibronectin, vitronectin, laminin, serum albumin
and collagen)
 Osteogenic cells attached to these binding motif using
membrane receptors (Integrins)
 Binding will provoke integrin-mediated cellular signaling
cascades and results in migration, proliferation and
differentiation of osteogenic cells. (Sawyer 2005)
33
Davies J. Mechanisms of Endosseous Integration. The International Journal of
Prosthodontics. 1998; 11(5): p. 391-401.
TIME COURSE OF INTERFACE DEVELOPMENT FOR
ENDOSSEOUS IMPLANTS IN CORTICAL BONE
Surface modeling
Stage 1: Woven callus 6 weeks
Stage 2: Lamellar compaction 18 weeks
Remodeling, maturation
Stage 3: interface remodeling 18 weeks
Stage 4: compact bone maturation 54 weeks
Misch C. Contemporary Implant Dentistry, 3e. 3rd ed.; 2008.
34
VIDEO
 Cell-to-Cell Communication - Osseointegration [Low,
240p].flv
35
REFERENCES
36
 Najjar T. FONSECA: oral and maxillofacial surgery. Reconstructive and
Implant surgery
 Branemark PI. Tissue-integrated prosthesis: osseointegration in clinical
dentistry Chicago: Quintessence Publishing Co.; 1985.
 Davies J. Mechanisms of Endosseous Integration. The International
Journal of Prosthodontics. 1998; 11(5): p. 391-401.
 Ramazanoglu M. Osseointegration and Bioscience of Implant Surfaces -
Current Concepts at Bone-Implant Interface, Implant Dentistry- A
Rapidly Evolving Practice Turkyilmaz PI, editor.: Intech; 2001.
 Misch C. Contemporary Implant Dentistry, 3e. 3rd ed.; 2008.

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Osseointegration part 1

  • 1. OSSEOINTEGRATION - PART I Dr Heenal Adhyaru Seminar No: 14
  • 2. CONTENT  INTRODUCTION  DEFINITIONS  BONE PHYSIOLOGY  TISSUE RESPONSE  MECHANISM OF OSSEOINTEGRATION  FACTORS AFFECTING OSSEOINTEGRAION  BIOMATERIALS  DESIGN CHARATERITICS  IMPLANT SURFACE  BONE DENSITY  SURGICAL TECHNIQUE  EVALUTION OF OSSEOINTEGRATION  CONCLUSION 2
  • 3. INTRODUCTION  Per-Ingvar Branemark in 1964  Dental implants for replacement of missing teeth.  Comparison with direct fracture healing. 3
  • 4. DEFINITION  “Direct structural and functional connection between ordered, living bone and surface of a load carrying implant” by Branemark et al. in 1977 .  “Functional ankylosis” by Schroeder et al. in 1981.  “A biomechanical phenomenon whereby clinically asymptomatic rigid fixation of the implant is achieved and maintained in bone during functional loading.” by Albrektson and Johansson in 2001. 4
  • 6. 6
  • 8. 8
  • 9. S 9
  • 10. TISSUE RESPONSE  Biological response to the host tissue following the placement of the implant: 1. Cellular injury 2. Inflammation and Coagulation 3. Repair and Regeneration 10
  • 11. CELLULAR INJURY injury: oxygen deprivation reversible injury: cellular swelling irreversible injury: point of no return 11 Najjar T. FONSECA: oral and maxillofacial surgery. Reconstructive and Implant surgery
  • 12. 12 Najjar T. FONSECA: oral and maxillofacial surgery. Reconstructive and Implant surgery
  • 13.  Injured mesenchymal cells at the surgical site are not conductive for osseointegration of the implant.  The aim is to reduce ischemia and anoxia to a minimal degree and for a very short duration during the surgical phase of implant placement. 13 Najjar T. FONSECA: oral and maxillofacial surgery. Reconstructive and Implant surgery
  • 15. 15
  • 16.  The micro-thrombin that are formed immediately after surgery at the implant bone interface constitute the framework for osseointegration to take place. 16 Najjar T. FONSECA: oral and maxillofacial surgery. Reconstructive and Implant surgery
  • 17. REPAIR AND REGENERATION Branemark PI. Tissue-integrated prosthesis: osseointegration in clinical dentistry Chicago: Quintessence Publishing Co.; 1985. 17  Bone may react in three different ways as a response to the necrosis
  • 18.  Conditions for bone repair at an implant site depend on the presence of: 1. Adequate cells 2. Adequate nutrition to these cells 3. Adequate stimulus for bone repair 18 Branemark PI. Tissue-integrated prosthesis: osseointegration in clinical dentistry Chicago: Quintessence Publishing Co.; 1985.
  • 19. ADEQUATE CELLS  Osteoclasts Creeping substitution Osteoblasts  Osteoclasts propagates at a rate of 50ɥm per day  Undifferentiated mesenchymal cells 19 Branemark PI. Tissue-integrated prosthesis: osseointegration in clinical dentistry Chicago: Quintessence Publishing Co.; 1985.
  • 20. ADEQUATE BONE CELL NUTRITION  Diffusion mechanism/ Angiogenesis  Cancellous bone: 100ɥm  Maximal vascular penetration rate:  Cancellous bone: 0.5mm/ day  Cortical bone: 0.05mm/ day 20 Branemark PI. Tissue-integrated prosthesis: osseointegration in clinical dentistry Chicago: Quintessence Publishing Co.; 1985.
  • 21. ADEQUATE STIMULUS FOR BONE REPAIR 21 Branemark PI. Tissue-integrated prosthesis: osseointegration in clinical dentistry Chicago: Quintessence Publishing Co.; 1985.
  • 22. STAGES OF OSSEOINTEGRATION 1. Incorporation by woven bone formation 2. Adaptation of bone mass to load (lamellar and parallel fibered bone deposition) 3. Adaptation of bone mass structure to load (bone remodeling) 22 Schenk RK. Osseointegration: a reality. Periodontology 2000. 1998; 17: p. 22- 35.
  • 23. WOVEN BONE FORMATION  The first bone tissue formed is woven bone. It is characterized by a random, felt-like orientation of its collagen fibrils, numerous, irregularly shaped osteocytes and, at the beginning, a relatively low mineral density  It grows by forming a scaffold of rods and plates and thus is able to spread out into the surrounding tissue at a relatively rapid rate.  Woven bone formation clearly dominates the scene within the first 4 to 6 weeks after surgery. 23 Schenk RK. Osseointegration: a reality. Periodontology 2000. 1998; 17: p. 22- 35.
  • 24. LAMELLAR AND PARALLEL FIBERED BONE DEPOSITION Lamellar bone deposition Parallel fibered bone deposition 24  The linear apposition rate:  1-1.5 ɥm/day  3-5 times larger than lamellar bone Schenk RK. Osseointegration: a reality. Periodontology 2000. 1998; 17: p. 22- 35.
  • 25.  Both types of bone grow by apposition on a preformed solid base.  Three surfaces are qualified as a solid base for deposition of parallel- fibered and lamellar bone:  Woven bone formed in the first period of osseointegration  Pre-existing or pristine bone surface  The implant surface. 25 Schenk RK. Osseointegration: a reality. Periodontology 2000. 1998; 17: p. 22- 35.
  • 26. BONE REMODELING  It starts around the third month and after several weeks of increasingly high activity, slow down again, but continues for the rest of life.  In cortical, as well as in cancellous bone, remodeling occurs in discrete units, often called a bone multicellular unit, as proposed by Frost.  Remodeling starts with osteoclastic resorption, followed by lamellar bone deposition. 26 Schenk RK. Osseointegration: a reality. Periodontology 2000. 1998; 17: p. 22- 35.
  • 27.  Remodeling in the third stage of osseointegration contributes; to an adaptation of bone structure to load in two ways:  It improves bone quality by replacing pre-existing, necrotic bone and/or initially formed more primitive woven bone with mature, viable lamellar bone.  It leads to a functional adaptation of the bone structure to load by changing the dimension and orientation of the supporting elements.  Continuous replacement of old bone by new bone prevents accumulation of micro-damage and fatigue as one possible cause of aseptic implant loosening. 27 Schenk RK. Osseointegration: a reality. Periodontology 2000. 1998; 17: p. 22- 35.
  • 28. MECHANISM OF INTEGRATION OSBORN AND NEWESLEY – 1980 Distance osteogenesis Contact osteogenesis 28 Davies J. Mechanisms of Endosseous Integration. The International Journal of Prosthodontics. 1998; 11(5): p. 391-401.
  • 29. MECHANISM OF INTEGRATION DAVIES - 1998  Contact osteogenesis:  Osteoconduction  De novo bone formation  Bone remodeling at discrete sites 29 Davies J. Mechanisms of Endosseous Integration. The International Journal of Prosthodontics. 1998; 11(5): p. 391-401.
  • 30. OSTEOCONDUCTION 30 Davies J. Mechanisms of Endosseous Integration. The International Journal of Prosthodontics. 1998; 11(5): p. 391-401.
  • 31.  Osborn (1979)categorized this bio-response into the following three groups:  Biotolerant type: characterized by distance osteogenesis, the implant is not rejected from the tissue, but it is surrounded by a fibrous connective tissue  Bioinert type: characterized by contact osteogenesis, the osteogenic cells migrate directly to the surface where they will establish de novo bone formation, and  Bioreactive type: the implant allows new bone formation around itself, thereby exchanging ions to create a chemical bond with the bone. 31 Davies J. Mechanisms of Endosseous Integration. The International Journal of Prosthodontics. 1998; 11(5): p. 391-401.
  • 32. DE NOVO BONE FORMATION 32 Secretion of two collagenous proteins: osteopontin and bone sialoprotein Calcium phosphate nucleation at the calcium binding sites of one or more of this protein. Crystal growth phase Collagen production and subsequent collagen mineralization Davies J. Mechanisms of Endosseous Integration. The International Journal of Prosthodontics. 1998; 11(5): p. 391-401.
  • 33.  Initial protein layer with arginine-glycine-aspartic acid motif adhesion. (Fibronectin, vitronectin, laminin, serum albumin and collagen)  Osteogenic cells attached to these binding motif using membrane receptors (Integrins)  Binding will provoke integrin-mediated cellular signaling cascades and results in migration, proliferation and differentiation of osteogenic cells. (Sawyer 2005) 33 Davies J. Mechanisms of Endosseous Integration. The International Journal of Prosthodontics. 1998; 11(5): p. 391-401.
  • 34. TIME COURSE OF INTERFACE DEVELOPMENT FOR ENDOSSEOUS IMPLANTS IN CORTICAL BONE Surface modeling Stage 1: Woven callus 6 weeks Stage 2: Lamellar compaction 18 weeks Remodeling, maturation Stage 3: interface remodeling 18 weeks Stage 4: compact bone maturation 54 weeks Misch C. Contemporary Implant Dentistry, 3e. 3rd ed.; 2008. 34
  • 35. VIDEO  Cell-to-Cell Communication - Osseointegration [Low, 240p].flv 35
  • 36. REFERENCES 36  Najjar T. FONSECA: oral and maxillofacial surgery. Reconstructive and Implant surgery  Branemark PI. Tissue-integrated prosthesis: osseointegration in clinical dentistry Chicago: Quintessence Publishing Co.; 1985.  Davies J. Mechanisms of Endosseous Integration. The International Journal of Prosthodontics. 1998; 11(5): p. 391-401.  Ramazanoglu M. Osseointegration and Bioscience of Implant Surfaces - Current Concepts at Bone-Implant Interface, Implant Dentistry- A Rapidly Evolving Practice Turkyilmaz PI, editor.: Intech; 2001.  Misch C. Contemporary Implant Dentistry, 3e. 3rd ed.; 2008.

Editor's Notes

  1. Modelling: net change in size and shape Remodelling: turnover or internal restructing Osteocytes: helps to control calcium and phosphate levels in the microenviroment and detect mechanical forces and translate them into biological activity- process called mechnao-transduction.
  2. Modelling / Remodelling Macrophage colony stimulating factor (M-CSF) precusor cell to osteoclasts Osteoclasts arise from hematopoietic precursors of monocytes/ macrophage lineage. Receptor activated nuclear factor KB All three belong to TNF superfamily
  3. The degree on injury depends on duration and degree of surgical trauma
  4. Oxygen deprivation: caused due to ischemia and activation of partially reduced oxygen species
  5. Increased intracellualer Ca. released for intracelluar stores, activity of protease and phospholipase, membrane damage-influx of extracelluar Ca, Ca leads to paralysis of ATP driven sodium pump…accumulation of intracelluar Na and diffusion of Potassium. Iso-osmotic gain of water Hypoxia continue…worsening mitochondria fun…increase permeability…..point of no return.
  6. Activation of clotting system, complement and kinin system
  7. Burheads The repair of the cortical necrotic border zone around an implant will to a large extent depends on one particular type of coupled osteoclasts/osteoblasts action called creeping substitution
  8. Cortical bone: Haversian canal (Alinged along long axis of the bone) Volkmann’s canal: perpendicular
  9. Burwell in 1966: dying cells differentiate mesenchymal cells or some differentiated cells remain alive Urist 1968 Yasuda 1953: Piezoelectric forces acted over the fracture gap and stimulate the bone healing
  10. Lamellar bone Packing of the collagen fibrils into parallel layers with alternating course gives it the highest ultimate strength Parallel-fibered bone is an intermediate between woven and lamellar bone: the collagen fibrils run parallel to the surface but without a preferential orientation in that plane
  11. . The term “Osteoconduction” refers to the migration of these cells to the proposed site. derived at bone remodeling sites from undifferentiated peri-vascular connective tissue cells. Fibrin retraction Fibrin the reaction product of thrombin and fibrinogen…adhere to implant surface and via which osteogenic cells migrate.
  12. 4 stages: Cement lines: non collagenous protein….interface between new and old bone….0.5micro meter thick Bonding of collagen and implant surface: interdigitation with chemically active surface….micromechanical interlocking.