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Guided by Presented by Prof. Neelam Mittal Dr. Isha Narang Dean and Head Junior resident Faculty of dental sciences Deptt. Of Endodontics IMS, BHU IMS , BHU VARANASI VARANASI
Regenerative endodontics is the creation and delivery of tissues to replace the diseased, missing and traumatized dental tissues.
Biologically based procedures designed to replace damaged structures, including dentin and root structures, as well as cells of pulp-dentin complex.
3
Regenerative endodontics has become a reality…. Approaches –Root-canal revascularizationPost-natal (adult) stem cell therapyPulp implantScaffold implantInjectable scaffolds Three-dimensional cell printing andGene therapy
REVASCULARIZATION
Introduced by Ostby in 1961 and reintroduced in 1966 by Rule and Winter.
Biologically based treatment regimen that offers, potential for continuous hard tissue formation in young permanent tooth with necrotic root canal system in addition to incompletely developed root
(Hargreaves et al 2008).
Why do we need Revascularization in Endodontics.
DENTAL TRAUMA
DENTAL CARIES
Poor crown root ratioThin dentinal walls
Calcium Hydroxide Apexification MTA apexification
Advantages
Revascularization
1] Elongation of root 2] Thickening of dentinal walls
PRINCIPLEThis is a ‘Tissue Engineering Concept’ (Nakashima & Akamine 2005).
Steps in Revascularization Disinfection of the root canal and periapical
area using Triple antibiotic paste Laceration of the periapical tissues Blood clot formation with the resultant
increase in growth factors like VEGF and platelet derived growth factors.
Huang GT, Lin LM. Letter to editor. J Endod 2008
Platelet concentrates are comprised of increased concentrations of TGF-β1 and are capable of increasing cell proliferation over time when compared with a blood clot (Lance et al 2010)
TGF-β and PDGF-AB
Soft tissue healing through collagen production Hard tissue healing through initiation of callus
formation and mineralization (Bolander 1992 and Cromack et al 1990).
SOURCES OF CONCENTRATED PLATELETS IN HAEMATOLOGY
It is further activated by adding bovine thrombin and calcium chloride for the activation.
METHOD OF PREPARATION
Division of blood sample in three layers:A base of red blood cells at the bottom, Acellular plasma on the topA clot of PRF in the middle
• In 2007, a new device for the preparation and standardization of leukocyte- and platelet-rich fibrin (L-PRF) clots and membranes was invented by Dr. Joseph Choukroun: the PRF Box (Process, Nice, France) (Ehrenfest 2010).
FIBRIN MESH OR MEMBRANE
ADVANTAGE
• No use of anticoagulants, thrombin and calcium chloride activators leads to formation of natural optimized fibrin clot.
(Tsay et al 2005).
PRF PRP
Significant release of 81% of cytokines within the first day with decreased release at 3, 7, and 14 days
Release occurs before
the initiation of outgrowth of osteoblasts
Slow continuous increase of cytokines like TGF-β1 and PDGF-AB
Peak level at 14 days coninciding with the cell ingrowth
TGF-β1 levels of PRP at day 1 were statistically higher than that of PRF at day 1 (P < .05).
STUDY ON RAT CALVARIA OSTEOBLASTS
EFFECT ON CELL NUMBER WITH DAYS PRF PRP
cell mineralization at point of day 14 (P < .05)
PRF PRP
Clinical application of PRPPRP mediated regeneration of vital tissues in
teeth with necrotic pulp and periapical radiolucency has been done
Torabinezad M. Revitalization of tooth with necrotic pulp and open apex by using Platelet rich plasma: A case report. J endod 2011;37:65-8.
INFERENCE The huge potential of concentrated growth
factors in the form of PRF may provide standardized degrees of hard and soft tissue healing in the periapical region matching the biochemical criteria of the clinical situation.
CASE REPORT 1
CONCLUSION
The huge potential of PRF must be understood as it helps in tissue healing in a fast, continuous and well controlled manner.