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Introduction

Terminologies

Bone graft

History

Mechanism of bone grafting

Clinical objectives of bone grafting for periodontal regeneration

Ideal properties of grafts

Indications of periodontal bone graft

(3)
(4)

Corrolline calcium carbonate

Combination procedures

Risk of disease transmission

Conclusion

(5)

INTRODUCTION

Periodontal diseases

(6)

TERMINOLOGY

Reattachment

New attachment

Periodontal repair

Periodontal regeneration

(7)

Historically, bone grafting has consisted of:

A surgical procedure to harvest the patients own bone from a secondary site

Utilization of an organic or artificial material to replace missing bone

Structural scaffolds &

matrices for attachment &

proliferation of anchorage

(8)
(9)
(10)

Formation and development of

new bone

by viable cells

contained in the graft

(11)

Provide a biologic stimulus (proteins and growth factors) that

induces the progression of mesenchymal stem cells and other

osteoprogenitor cells toward the osteoblast lineage

(12)

Is the process by which the graft material acts as a

nonviable

scaffold

onto and within which the patients own natural bone

grows

They allow apposition from existing bone, but

do not produce

or trigger bone formation.

(13)

Osteopromotion

Osteopromotion

Osteopromotion

involves

the

enhancement

of

osteoinduction without the possession of osteoinductive

(14)

Clinical objectives of bone grafting for periodontal regeneration

In a review of animal histologic studies, Mellonig found that 75% of these

studies indicated favorable regenerative results when periodontal

defects were treated with grafting; none showed that non-graft control

sites were superior to grafted ones.

(15)

 Non-toxic-Non-antigenic with patient acceptance

 Resistant to infection

 Facilitate vascularization

 No root resorption or ankylosis

 Strong and resistant

Stimulates osteoinduction- & framework for osteoconduction

(16)

 Readily and sufficiently available

 Minimal surgical procedure with minimal post-operative sequelae

 Predictability

Completely replaced by host bone of the same quality – quantity

Induce & enhance cementogenesis.

CONTD..,

(17)

Indications of periodontal bone graft

1.Deep intraosseous defect

2.Tooth retention

3.Support for critical teeth

4.Defects

associated

with

aggressive

periodontitis

5.Esthetics

(18)

Classification

 Conge et al, 1978

 AAP 1986

 Carranza FA 1990

 Rosenberg& Rose 1998

(19)

Resorption of the graft and replacement by new bone

depends upon

Particle size

(20)

Xenografts

(21)

CALF BONE - treated by detergent, sterilized and freeze dried. Used for treatment

of osseous defects.

KIEL BONE - Calf or Ox bone denaturated with 20% H

2O2, dried with acetone, and

sterilized with ethylene oxide.

ANORGANIC BONE - Ox bone from which the organic material has been extracted by

ethylene diamine. Then sterilized by autoclaving.

Recently a natural, anorganic, microporous, bovine-derived hydroxyapatite bone

matrix, in combination with a cell-binding polypeptide that is a synthetic clone of 15

(22)

ANORGANIC BOVINE

BONE(ABB

(

New processing and purification methods have been

(23)

Osteoconductive

Chemical & physical characteristics

similar to human mineral matrix

Porosity similar to human cancellous

bone

Large mesh interconnecting pore

system

facilitates angiogenesis and

migration of osteoblasts.

(24)
(25)

USES:

1. Treatment of defect sizes up to 2 alveoli, but can be used for

defect size larger than 2 alveoli.

2. Sinus floor elevations.

3. When combined with autogenous bone, it can be used for large

ridge augmentation.

(26)

Bio – Oss Collagen

® (Osteohealth Co., Shirley, NY)

Bio Oss spongiosa granules + 10% highly purified porcine collagen

Collagen component enables

convenient handling to be easily

adapted in the defect but does not function as a barrier

(27)

Studies

Stefano Sartori et al.,

analyse the amount of Bio-Oss

ossification in a case of maxillary sinus augmentation,

recording and comparing histomorphometric data 8 months, 2

and 10 years after surgery.

Eight months after surgery they observed a mean amount of bone tissue

(including medullar spaces) of 29.8% (and 70.2% of Bio-Oss) . At 2years the

(28)

Effect of low-level laser therapy irradiation and Bio-Oss graft

material on the osteogenesis process in rabbit calvarium defects:

a double blind experimental study- Alireza Rasouli et al., 2014

The mean amount of new bone was 15.83 and 18.5 % in the controls on the

4th and 8th week; 27.66 and 25.16 % in the laser-irradiated group; 35.0

and 41.83 % in Bio-Oss and 41.83 and 47.0 % in the laser + Bio-Oss

treated specimens with significant statistical differences.

Application of

(29)

ABB plus P-15 cell binding

peptide

(pentadecapeptide)

Mimics the cell binding

domain of

type I collagen

(30)

Hanadi Baeissa

(31)

Clinical and radiographic evaluation of human periodontal

osseous defect (mandibular grade II furcation) treated with

PepGen P-15 and a bioresorbable membrane (Atrisorb)-

2012 KL

Vandana et.,al .

It can be concluded from this study that the reduction in furcation

defect using PepGen P-15 alone and a combination of PepGen P-15

and Atrisorb were equivocal. It can be suggested that the combined

use of GTR barrier and bone graft did not prove beneficial for the

clinical outcome of the mandibular grade II furcation defect

treatment. Hence, the cost effective and economical treatment of

(32)

A Novel Combination Of Platelet Rich Fibrin And Pepgen P-15

Dentascanimages acquired at 9 month interval, confirmed positive

changes in the defect morphology, with a linear bone growth of

1.5-3mm( 33 to 37 %).The volumetric analysis showed a bone fill of 55 to

(33)

Interdisciplinary Management of an Isolated Intrabony Defect- 2014

A 24 year male patient reported with the complaint of food lodgment and occasional pain in relation to right lower first molar. Clinical examination

(34)

Treatment of Intrabony Defects with Anorganic Bone Matrix/P-15

or Guided Tissue Regeneration in Patients with Aggressive

Periodontitis -2013

Treatment of intrabony periodontal defects in patients with

G-AgP with ABM/P-15 and GTR improved significantly the clinical

outcomes. The use of ABM/P-15 promoted a better

(35)

Porcine derived bone graft:

Xenografts derived from porcine cortical and cancellous bone

have also been developed to be used as bone substitutes

OsteoBiol® It is a commercially available xenograft of porcine origin.

It is heterologous cortico cancellous collagenated bone mix. It always

(36)

Advantages:

It can act as a carrier for various therapeutic agents.

The collagen present in this bio material facilitates blood clotting

and the subsequent invasion of repairing and regenerative cells thus

favouring bone formation.

(37)

Experimental Model of Bone Response to Collagenized Xenografts

of Porcine Origin (OsteoBiol® mp3): A Radiological and

Histomorphometric Study

After 4 months, radiological images revealed bone defects with

a decrease in graft volume and the complete repair of the

osseous defect.

The

biomaterial

used

proved

to be biocompatible,

bioabsorbable, and osteoconductive and as such, a possible

bone substitute that did not interfere with the bone’s normal

(38)

CORROLLINE CALCIUM CARBONATE

Biocoral is a calcium carbonate

Natural coral,

Primarily of aragonite.

It is biocompatible and resorbable

(39)

Combination procedures

A combination of autogenous bone and bone substitute is widely used in

oral surgery procedures

Systematic review recommended a proportion of 1:2 (Merkx et al. 2003).

Pripatnanont et al. (2009) assessed new bone formation generated using

three different proportions of autogenous bone (AB) and deproteinized

bovine bone (BDX) in cortical skull defects in rabbits.

(40)

In deep intrabony defects treatment, at 12 months evaluation,

the combined use of autogenous spongiosa with bovine-derived

xenograft led to significantly greater gain of clinical attachment and

hard tissue formation compared to the use of autogenous

spongiosa alone

(41)

Efficacy of Using PDGF and Xenograft With or Without Collagen

Membrane for Bone Regeneration Around Immediate Implants

With Induced Dehiscence-Type Defects: A Microcomputed

Tomographic Study in Dogs- 2013

GBR around immediate implants with dehiscence defects using PDGF

and xenograft alone resulted in higher BBT, BBV, VBH, and BIC than

(42)

A clinical and radiological evaluation of the relative efficacy of

demineralized freeze-dried bone allograft versus anorganic bovine bone

xenograft in the treatment of human infrabony periodontal defects: A 6

months follow-up study- 2014

The use of anorganic bovine bone mineral matrix combined with TGFβ-1

seemed to be effective in the treatment of intrabony defects. This showed an

improvement in the clinical outcome of periodontal therapy superior to the use

(43)

Risk of transmission of

prion mediated diseases

– bovine

spongiform encephalopahty

In humans –

Creutzfeldt – Jakob disease

WHO – bone as

type IV

(no transmission)for prion diseases

Segal and Tofe (1999)

conducted an extensive review of current

literature on the status of risk assessment of BSE transmission the

risk of disease (BSE) transmission was

negligible

(44)
(45)

CONCLUSION

Although complete periodontal regeneration is unpredictable with any

regenerative therapy currently used, periodontal bone grafts show strong

potential. Requirements for a successful graft includes Patient Selection,

material Selection, Proper Flap Reflection and Wound Stability,

Revascularization, Root Debridement, Postsurgical care .A large body of

clinical evidence clearly indicates that grafts consistently lead to better bone

fill than nongrafted controls. As more is learned about the biologic process of

periodontal regeneration, new graft materials are expected to make the task

(46)

REFERENCES

•Nasr HF, Reidy AME, Yukna RA. Bone and bone substitutes. Periodontology

2000, 1999; 19: 74-86.

•Carranza FA, Takei HH, Cochran DL. Chapter-67, Reconstructive Periodontal

Surgery. Carranza's Clinical Periodontology, 10th edition: 968-969.

•Reynolds MA, Reidy AME, Branch-May GL, Gunsolley JC. The efficacy of bone

replacement grafts in the treatment of periodontal osseous defects. Ann

Periodontol 2003; 8(1): 227-265.

•Dental & Medical Device. Product information on Osteo-Biol ®, 2008.

(47)

•Rita Singh, Lanka Mahesh. Infections Resulting from Bone Grafting Biomaterials.

International Journal of Oral Implantology and Clinical Research, May-August

2013;4(2):68-71

•A.L. Dumitrescu, Chemicals in Surgical Periodontal Therapy, Bone Grafts and

Bone Graft Substitutes in Periodontal Therapy.

•Emmings et al. Chemically modified osseous material for restoration of bone

defects. J Periodontol 1974; 45:385.

•Boyne et al. Transplantation, implantation and grafts. Dent Clin N Am 1971; 15:

434.

•Krejci et al. Osseous grafting in periodontal therapy. Part I - Osseous graft

(48)

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