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1
Greatest challenges to the integrity 
of the developing tooth 
2
Primary goal 
Maintain pulp vitality 
Normal tooth development 
3
History 
• 1746 - Philip Pfaff a dentist to King Frederick of Prussia first mentioned capping an 
exposed pulp before inserting a filling 
• 1800’s, - clinicians utilized metal-caps covered with chlora-percha as a temporary 
“stopping” agent to clinically treat an exposed pulp 
• 1826 - Koecker recommended that an exposed pulp be cauterized with a red-hot 
wire before covering with gold leaf and the cavity filled with gold 
• 1900- Jack gave the name “direct pulp capping”, came from the clinical placement 
of small metal caps over an exposed pulp 
• 1920 – Hermann – Ca(OH)2 
4
Key responses of the dentin-pulp to caries / injury 
Tertiary dentin 5
Reactionary dentinogenesis 
Caries 
Odontoblasts 
Dentin 
Tertiary, reactionary dentin laid 
6
Reparative dentinogenesis 
Tertiary, 
reparative dentin 
7
Remaining Dentinal Thickness/ Effective Depth 
• RDT is a key determinant of pulp survival after cavity preparation & avoiding pulp 
exposure has been considered advantageous. 
Int Endod J 41:389, 2008. 
8
9
Determining the pulpal status of cariously involved teeth involves the following: 
1. Visual & tactile examination of carious dentin and associated periodontium 
2. Radiographic examination 
3. History of spontaneous unprovoked pain 
4. Pain from percussion 
5. Pain from mastication 
6. Degree of mobility 
7. Palpation of surrounding soft tissues 
8. Size, appearance & amount of hemorrhage associated with pulp exposures 
10 
Endodontics : Ingle 5th edi
The outcome of VPT depends on: 
- Type of injury 
- age of the pt 
- size & location of the pulp exposure 
- bacterial contamination 
- pulp capping material & 
- quality of the final restoration 
11
12 
Vital pulp therapy 
Indirect pulp 
capping 
Direct pulp 
capping 
Pulpotomy
13
Indirect pulp capping 
Definition: IPC is a procedure wherein the deepest layer of the remaining 
affected carious dentin is covered with a layer of biocompatible material in order 
to prevent pulpal exposure & further trauma to the pulp. 
Aims of indirect pulp capping : 
• To arrest the carious process, 
• Provide conditions conducive to the formation of reactionary 
dentin, and 
• Promote remineralization of the altered dentin that was left. 
• Promote pulpal healing & preserve/maintain the vitality of the pulp. 
14
• When pulpal inflammation has been judged to be minimal & complete removal of 
caries would cause pulp exposure. 
• Mild pain associated with eating. 
• Negative history of spontaneous, extreme pain. 
• When there is a definite layer of affected dentin after removal of infected dentin. 
• Deep carious lesion, which are close to, but not involving pulp in vital primary or young 
permanent teeth 
15
• Any signs of pulpal or periapical pathology. 
• Soft leathery dentin covering a very large area of the cavity, in a non restorable tooth. 
• Sharp, penetrating pulpalgia 
• Prolonged night pain. 
• Mobility of the tooth. 
• Discoloration of the tooth. 
• Definite pulp exposure. 
• Interrupted or broken lamina dura. 
• Radiolucency about the apices of the roots 
16
• Hard setting Ca(OH)2 
• ZOE 
• GIC (Glass ionomer caries control approach) 
• Resin modified glass ionomer 
• Bonded composite 
• MTA 
17
• IPC studies show success rates of 90% or greater over time with differing 
techniques and medicaments. 
IPT medicaments Success 
(%) 
Time (mo) Sample 
(N) 
J Endod Vol 34, No 7S, July 2008 
Nirschl and Avery 
1983 
Calcium hydroxide 94 6 33 
Al-Zayer et al. 2003 Calcium hydroxide 95 14 (median) 187 
Vij et al. 2004 Glass ionomer 94 40 108 
Farooqet al. 2000 Glass ionomer 93 50 55 
18
• To manage lesions in primary molars (that are 
symptom free and free from radiographic signs of 
periradicular pathology) by cementing a preformed 
metal (stainless steel) crown in place without local 
anaesthesia, tooth preparation, or any attempt at 
caries removal. 
Innes NP, Stirrups DR, Evans DJ, Hall N, Leggate M: A novel technique 
using preformed metal crowns for managing carious primary molars in 
general practice–a retrospective analysis. Br Dent J 200:451, 2006 
• After a review period of 2 years, comparing the 
teeth managed using Hall preformed metal 
(stainless steel) crowns with conventional 
restorations, the “Hall crowns” showed better 
treatment outcomes for both pulpal health and 
restoration longevity. 
Innes NP, Evans JP, Stirrups DR: The Hall technique; a randomized 
controlled clinical trial of a novel method of managing carious primary 
molars in general dental practice: acceptability of the technique and 
outcomes at 23 months. BMC Oral Health 7:18, 2007. 19
• Two appointment technique 
• One appointment technique 
20
• Researchers continue to investigate the role of antimicrobial treatments, 
including 
• Ozone fumigation, Eur J Oral Sci 114:349, 2006 
• Photo-activated disinfection (PAD), and 
• Antimicrobial resins in sterilizing deep layers of affected dentin & creating the 
conditions for arresting and remineralisation. 
Int Endod J 40:58, 2007. 
• Considerable interest has also focused on the active upregulation of reactionary 
dentinogenesis by applying bioactive agents such as the TGF-β family of 
molecules to the depths of cavity preparations. 
Caries Res 38:314, 2004. 
21
Guideline on Restorative Dentistry 
Recommendations 
American Academy of Pediatric Dentistry (AAPD) & American Association of Endodontists (AAE) 
1. There is evidence from randomized controlled trails and systematic reviews that 
incomplete caries excavation in primary and permanent teeth with normal 
pulps or reversible pulpitis, either partial (one step) or stepwise (two step) 
excavation, results in fewer pulp exposures and fewer signs and symptoms of 
pulpal disease than complete excavation. 
2. There is evidence that partial excavation (one step) followed by placement of 
final restoration leads to higher success in maintaining pulp vitality in 
permanent teeth than stepwise (two-step) excavation. 
22 
2014
23
Def: Direct pulp capping involves the 
placement of a biocompatible agent on 
healthy pulp tissue that has been 
inadvertently exposed from caries 
excavation or traumatic injury. 
Oral Surg 1972;34:477. 
Objective: To seal the pulp against bacterial leakage, 
encourage the pulp to wall off the exposure site by initiating a dentin 
bridge, and maintain the vitality of the underlying pulp tissue regions. 
24
1. Small pin point mechanical exposures of diameter < 1.0mm 
2. Pulp exposed without previous symptoms of pulpitis. 
25
(1) Spontaneous & nocturnal toothaches. 
(2) Excessive tooth mobility. 
(3) Thickening of the PDL. 
(4) Radiographic evidence of furcal or periradicular degeneration. 
(5) Uncontrollable hemorrhage at the time of exposure, and 
(6) purulent or serous exudate from the exposure. 
26
• Ca(OH)2 
• ZOE 
• Corticosteroids & Antibiotics 
• Polycarboxylate cements 
• Collagen fibers 
• Formocresol 
• Bonding agents 
• MTA 
• Biodentine 
• Calcium enriched mixture 
• Bioactive glass 
• Enamel matrix derivates 
• Bioactive molecules 
• Miscellaneous 
27
Calcium Hydroxide - gold standard 
Hermann (1920) - introduced the use of 
CaOH2 as a clinical procedure to stimulate pulp 
healing and dentin bridge formation.
Mechanism: 
CH – high alkaline medium 
Coagulation necrosis of the surface of the 
enzyme alkaline 
phosphatase 
pulp 
Inorganic phosphate and calcium from the 
blood (Pisanti & Sciaky 1964) 
Precipitation of calcium 
phosphate
Disadvantages of Ca(OH)2 
 Presence of tunnel defects in dentin barrier. 
 Extensive dentin formation. 
 High solubility in oral fluids. 
 Lack of adhesion & degradation after acid etching. 
Asgary et al, 2008, 
Cox et al, 1985, 
Pitt ford, Roberts 1991 
30
• Pulp capping with MTA is recommended for teeth with carious pulp exposures specially immature teeth 
with high potential for healing. 
Farsi N, et al 2006 
• MTA is superior in terms of dentin bridge formation during the early healing process in human dental 
pulp. 
Min et al, 2008 
• MTA seemed to heal the pulp tissue at a faster rate than CH cement in human teeth. 
Accornite et al, 2008 
• MTA was clinically easier to use as a direct pulp capping agent and resulted in less pulpal inflammation 
and more predictable hard tissue barrier formation than Dycal. 
Nair PN et al, 2009 
• It has excellent sealing ability. 
Torabinejad et al, 1993, 1994, Bates et al, 1996, Fischer et al, 1998, Wu et al, 1998. 
• Biocompatibility. 
Kettering & Torabinejad 1995, Torabinejad et al, 1997, 1998, Holland et al, 1999, Mitchell et al, 1999, Keiser et al, 
2000 
31
Mechanism……………………… 
Calcium oxide present in MTA + tissue fluids calcium hydroxide 
calcite crystals 
attract fibronectin, which is responsible for cellular 
adhesion and differentiation 
(“Holland et al 1999”) 
Calcium ions released from MTA + phosphate in tissue fluid hydroxapatite
initial deep caries and immature apices 
Pulpal exposure 
Five-minute application of 5.25% sodium hypochlorite 
hemostasis, on two 1.5- to 2.0-mm exposures 
33
Radiograph of molar with MTA after 
initial visit 
Radiograph taken at the 5.5-year recall 
appointment showing permanent 
restoration and evidence of complete 
root formation. 
(From Bogen G, Kim JS, Bakland LK: Direct pulp capping with mineral trioxide 
aggregate. An observational study. J Am Dent Assoc 139:305-315, 2008. 34
• On the biological level, it is perfectly biocompatible & capable of inducing the apposition of reactionary 
35 
dentin by stimulating odontoblast activity & reparative dentin, by induction of cell differentiation . 
Laurent et al., 2008., 
Goldberg et al., 2009., 
Shayegan et al., 2010 
• It is an effective dentin substitute that can be used as a coronal restoration material (for indirect pulp 
capping), but can also be placed in contact with the pulp. 
• Its faster setting time allows either immediate crown restoration, or to make it directly intraorally 
“functional” without fear of the material deteriorating. 
Tran et al., 2008 
• Biodentine™ significantly increased TGF- β1 secretion from pulp cells independently of the contact 
surface compared to the increase by Ca(OH)2 & MTA. 
Laurent P, Camps J, About I: Int Endod J; May 2012, Vol. 45 Issue 5, p439-448.
Clinical view Distal pulp horn involvement 
After removal of restoration Biodentine placement 
36
Post--‐operative clinical view Post‐operative X‐ray follow‐up image 
Ceramic onlay, final restoration 
after 2 months 
Post ‐operative X‐ray follow‐up image 
37 
Courtsey: Dr. Lucile Goupy
• Antibacterial effect comparable to CH & superior to MTA 
Asgary S, Kamrani FA 2008 
• Sealing ability similar to MTA 
Asgary S, Eghbal MJ, Parirokh M 2008 
• Biologic response of pulp to MTA & CEM cement - similar in dogs’ teeth. 
Asgary S et al, 2008 
• CEM cement provides an endogenous source of calcium & phosphate ions that accelerates 
hydroxyapatite (HA) crystal formation as a second-seal on its surface even in normal saline storage 
media. 
Aust Endod J 2009;35:147–52. 
• Set form of CEM cement is similar to dentin. 
J Endod 2009;35:243–50. 
38
• Hench – 1969 
• Bioglass® 45S5  45wt% SiO2, 24.5wt% Na2O & CaO, and 6wt% P2O5. 
• React with aqueous solutions & produce a carbonated apatite layer. 
dentin 
• BAG can be the material of choice for pulp capping & periapical bone healing because it is 
biocompatible & has antibacterial property. 
Schepers et al, 1991 
• BAG produce Less inflammation, dentin bridge formation & no internal resorption, necrosis or abscess 
compared to Ca(OH)2 
Journal of Dentistry, Tehran University of Medical Sciences, Tehran, Iran (329007)
• Enamel Matrix Derivative (EMD) is a rich Amelogenin & Amelin biomaterial that has been 
demonstrated to induce a reparative process similar to normal odontogenesis when placed in 
contact with pulp tissue. 
• MTA produced a better quality reparative hard tissue response with the adjunctive use of Emdogain, 
when compared with the use of calcium hydroxide. 
J Endod 35 , Pages 667-672, May 2011 
40 
Amelogenins form a matrix layer on the surface. 
Contact to cells of the healthy part of the dentin 
The cells secrete natural and specific cytokines and autokrine 
substances, which promote the required proliferation 
Adduction and proliferation of mesenchymal cells from the 
healthy part of the dentin 
Attraction and differentiation of odontoblasts, begin the 
formation of the matrix
• Consists of Calcium silicates, Monobasic calcium phosphate, zirconium oxide, tantalum oxide 
• Hirschman et al compared Cytotoxicity of MTA-Angelus, Brasseler Endosequence Root Repair 
Putty (ERRP), Dycal & Ultra-blend Plus (UBP)-(light curable Ca(OH)2 & concluded that ERRP & 
UBP are less cytotoxic 
J Endod 2012 
41
• Light-cured resin-modified calcium silicate pulp protectant 
• Immediate placement & condensation. 
• TheraCal displayed higher calcium-releasing ability & lower solubility than either ProRoot 
MTA or Dycal. 
• The capability of TheraCal to be cured to a depth of 1.7 mm may avoid the risk of untimely 
dissolution. 
Int Endod J , 45: 571–579, June 2012. 
42
Bioactive molecules 
1. Bone Sialoprotein (BSP) 
2. Bone Morphogenetic Protein-7 (BMP-7), also termed 
Osteogenic Protein-1 (OP-1) 
“M. Goldberg et al - Adv Dent Res August 2001”
44 
BSP & BMP 
implanted in the pulp 
recruitment of cells bearing an osteoblastic phenotype 
(i.e which differentiate into osteoblast like cells ) 
Produces a mineralizing extracellular matrix. 
Atubular Dentin dense layer.
Miscellaneous 
• TGF-b1 
 Enhances reparative dentin formation 
Hu et al - J Endod. 1998 
• Recombinant Insulin Like Growth Factor-I 
 rhIGF-I in rat molars resulted dentin bridge formation equal to dycal 
after 28 days 
Lovschall H, et al - J Endod. 2008 
• Odontogenic Ameloblast Associated Protein (ODAM) 
 rODAM accelerates reactionary dentin formation close to the pulp exposure area, 
thereby preserving normal odontoblasts in the remaining pulp 
Yang IS et al - J Endod. 2010 
45
46
Def: “amputation of the affected or infected coronal portion of the dental pulp, 
preserving the vitality & function of all or part of the remaining radicular 
pulp”. 
AAPD guidelines 2014 
47
• Caries removal results in pulp exposure in a primary tooth with a normal pulp or 
reversible pulpitis or after a traumatic pulp exposure. 
• Radicular tissue is judged to be vital without suppuration, purulence, necrosis, or 
• Excessive hemorrhage that cannot be controlled by a damp cotton pellet after several 
minutes, 
• No radiographic signs of infection or pathologic re-sorption. 
48
According to Mejare: 
• Resorption exceeding >1/3rd of the root length 
• Nonrestorable tooth crown 
• Highly viscous, sluggish, or absent hemorrhage at the radicular canal orifices 
• Marked tenderness to percussion 
• Mobility with locally aggravated gingivitis associated with partial or total radicular pulp 
necrosis 
• Radiolucency in the furcal or periradicular areas 
• Persistent toothaches & coronal pus 
49
CLASSIFICATION 
 Amount of pulpal tissue involved 
 Cervical / Complete Pulpotomy 
 Partial pulpotomy [Cvek’s pulpotomy] 
 Type of medicament employed 
Grossman’s Endodontic Practice 12th Edition
CLASSIFICATION 
Pedodontics – Shobha Tandon 2nd Edition 
51 
Types Other name Features Examples 
Devitalization 
Preservation 
Regeneration 
Mummification, 
cauterization 
Minimal 
devitalization, 
noninductive 
Inductive, 
reparative 
It is intended to 
destroy or mummify the 
vital tissue. 
This implies maintaining 
the maximum vital 
tissue,with no induction 
of reparative dentin. 
This has formation of 
dentin bridge. 
Single sitting 
Formocresol 
Electrosurgery 
Laser 
Two stage 
Gysi triopaste 
Easlick’s formaldehyde 
Paraform devitalizing paste 
ZnO Eugenol 
Glutaraldehyde 
Ferric sulphate 
Ca(OH)2 
Bone morphogenic protein 
Mineral trioxide aggregate 
Enriched collagen 
Freezed dried bone 
Osteogenic protein
Agents for 
pulpotomy 
Pharmacotherapeutic 
Formocresol 
Glutaraldehyde 
Calcium hydroxide 
Collagen 
Ferric sulfate 
CaPo4 cement 
Hydroxyapatite 
BMP 2 & 4 
Freeze dried bone 
MTA 
CEM 
Biodentine 
Non-pharmacologic 
Electro surgery 
Lasers 
52
MTA & Formocresol 
JOE—Volume 34, Number 7, July 2008 
53
Ferric sulphate & Formocresol 
JOE—Volume 34, Number 7, July 2008 
54
CH & FC 
JOE—Volume 34, Number 7, July 2008 
55
Laser vs FC 
56 
Clinical (%) Radiograhic (%) 
Nd:YAG laser 97 94 
FC 85 78 
• The permanent successors of the laser-treated teeth erupted without any 
complications. 
J Endod, 2006: 32:404-7
NaOCl vs FS 
Vargas et al, 2006 
Duration Ferric sulphate NaOCl 
Paediatr Dent 2006, 28: 511-7 
Clinical 
success 
Radiographic 
success 
Clinical 
success 
Radiographic 
success 
At 6 months 100% 68% 100% 91% 
At 12 months 85% 62% 100% 79% 
57
• Case reports showing successful pulpotomy with MTA 
18 month 
19 month 
58 
JADA, Vol. 137 May 2006
Case report showing successful pulpotomy with 
CEM cement in permanent molar with irreversible 
pulpitis & condensing apical periodontitis: 
Saeed Asgary. J Conser Dent 2011, 14: 90-93 
6 months 
1 year 2 years 
59
60

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Vital Pulp Therapy

  • 1. 1
  • 2. Greatest challenges to the integrity of the developing tooth 2
  • 3. Primary goal Maintain pulp vitality Normal tooth development 3
  • 4. History • 1746 - Philip Pfaff a dentist to King Frederick of Prussia first mentioned capping an exposed pulp before inserting a filling • 1800’s, - clinicians utilized metal-caps covered with chlora-percha as a temporary “stopping” agent to clinically treat an exposed pulp • 1826 - Koecker recommended that an exposed pulp be cauterized with a red-hot wire before covering with gold leaf and the cavity filled with gold • 1900- Jack gave the name “direct pulp capping”, came from the clinical placement of small metal caps over an exposed pulp • 1920 – Hermann – Ca(OH)2 4
  • 5. Key responses of the dentin-pulp to caries / injury Tertiary dentin 5
  • 6. Reactionary dentinogenesis Caries Odontoblasts Dentin Tertiary, reactionary dentin laid 6
  • 8. Remaining Dentinal Thickness/ Effective Depth • RDT is a key determinant of pulp survival after cavity preparation & avoiding pulp exposure has been considered advantageous. Int Endod J 41:389, 2008. 8
  • 9. 9
  • 10. Determining the pulpal status of cariously involved teeth involves the following: 1. Visual & tactile examination of carious dentin and associated periodontium 2. Radiographic examination 3. History of spontaneous unprovoked pain 4. Pain from percussion 5. Pain from mastication 6. Degree of mobility 7. Palpation of surrounding soft tissues 8. Size, appearance & amount of hemorrhage associated with pulp exposures 10 Endodontics : Ingle 5th edi
  • 11. The outcome of VPT depends on: - Type of injury - age of the pt - size & location of the pulp exposure - bacterial contamination - pulp capping material & - quality of the final restoration 11
  • 12. 12 Vital pulp therapy Indirect pulp capping Direct pulp capping Pulpotomy
  • 13. 13
  • 14. Indirect pulp capping Definition: IPC is a procedure wherein the deepest layer of the remaining affected carious dentin is covered with a layer of biocompatible material in order to prevent pulpal exposure & further trauma to the pulp. Aims of indirect pulp capping : • To arrest the carious process, • Provide conditions conducive to the formation of reactionary dentin, and • Promote remineralization of the altered dentin that was left. • Promote pulpal healing & preserve/maintain the vitality of the pulp. 14
  • 15. • When pulpal inflammation has been judged to be minimal & complete removal of caries would cause pulp exposure. • Mild pain associated with eating. • Negative history of spontaneous, extreme pain. • When there is a definite layer of affected dentin after removal of infected dentin. • Deep carious lesion, which are close to, but not involving pulp in vital primary or young permanent teeth 15
  • 16. • Any signs of pulpal or periapical pathology. • Soft leathery dentin covering a very large area of the cavity, in a non restorable tooth. • Sharp, penetrating pulpalgia • Prolonged night pain. • Mobility of the tooth. • Discoloration of the tooth. • Definite pulp exposure. • Interrupted or broken lamina dura. • Radiolucency about the apices of the roots 16
  • 17. • Hard setting Ca(OH)2 • ZOE • GIC (Glass ionomer caries control approach) • Resin modified glass ionomer • Bonded composite • MTA 17
  • 18. • IPC studies show success rates of 90% or greater over time with differing techniques and medicaments. IPT medicaments Success (%) Time (mo) Sample (N) J Endod Vol 34, No 7S, July 2008 Nirschl and Avery 1983 Calcium hydroxide 94 6 33 Al-Zayer et al. 2003 Calcium hydroxide 95 14 (median) 187 Vij et al. 2004 Glass ionomer 94 40 108 Farooqet al. 2000 Glass ionomer 93 50 55 18
  • 19. • To manage lesions in primary molars (that are symptom free and free from radiographic signs of periradicular pathology) by cementing a preformed metal (stainless steel) crown in place without local anaesthesia, tooth preparation, or any attempt at caries removal. Innes NP, Stirrups DR, Evans DJ, Hall N, Leggate M: A novel technique using preformed metal crowns for managing carious primary molars in general practice–a retrospective analysis. Br Dent J 200:451, 2006 • After a review period of 2 years, comparing the teeth managed using Hall preformed metal (stainless steel) crowns with conventional restorations, the “Hall crowns” showed better treatment outcomes for both pulpal health and restoration longevity. Innes NP, Evans JP, Stirrups DR: The Hall technique; a randomized controlled clinical trial of a novel method of managing carious primary molars in general dental practice: acceptability of the technique and outcomes at 23 months. BMC Oral Health 7:18, 2007. 19
  • 20. • Two appointment technique • One appointment technique 20
  • 21. • Researchers continue to investigate the role of antimicrobial treatments, including • Ozone fumigation, Eur J Oral Sci 114:349, 2006 • Photo-activated disinfection (PAD), and • Antimicrobial resins in sterilizing deep layers of affected dentin & creating the conditions for arresting and remineralisation. Int Endod J 40:58, 2007. • Considerable interest has also focused on the active upregulation of reactionary dentinogenesis by applying bioactive agents such as the TGF-β family of molecules to the depths of cavity preparations. Caries Res 38:314, 2004. 21
  • 22. Guideline on Restorative Dentistry Recommendations American Academy of Pediatric Dentistry (AAPD) & American Association of Endodontists (AAE) 1. There is evidence from randomized controlled trails and systematic reviews that incomplete caries excavation in primary and permanent teeth with normal pulps or reversible pulpitis, either partial (one step) or stepwise (two step) excavation, results in fewer pulp exposures and fewer signs and symptoms of pulpal disease than complete excavation. 2. There is evidence that partial excavation (one step) followed by placement of final restoration leads to higher success in maintaining pulp vitality in permanent teeth than stepwise (two-step) excavation. 22 2014
  • 23. 23
  • 24. Def: Direct pulp capping involves the placement of a biocompatible agent on healthy pulp tissue that has been inadvertently exposed from caries excavation or traumatic injury. Oral Surg 1972;34:477. Objective: To seal the pulp against bacterial leakage, encourage the pulp to wall off the exposure site by initiating a dentin bridge, and maintain the vitality of the underlying pulp tissue regions. 24
  • 25. 1. Small pin point mechanical exposures of diameter < 1.0mm 2. Pulp exposed without previous symptoms of pulpitis. 25
  • 26. (1) Spontaneous & nocturnal toothaches. (2) Excessive tooth mobility. (3) Thickening of the PDL. (4) Radiographic evidence of furcal or periradicular degeneration. (5) Uncontrollable hemorrhage at the time of exposure, and (6) purulent or serous exudate from the exposure. 26
  • 27. • Ca(OH)2 • ZOE • Corticosteroids & Antibiotics • Polycarboxylate cements • Collagen fibers • Formocresol • Bonding agents • MTA • Biodentine • Calcium enriched mixture • Bioactive glass • Enamel matrix derivates • Bioactive molecules • Miscellaneous 27
  • 28. Calcium Hydroxide - gold standard Hermann (1920) - introduced the use of CaOH2 as a clinical procedure to stimulate pulp healing and dentin bridge formation.
  • 29. Mechanism: CH – high alkaline medium Coagulation necrosis of the surface of the enzyme alkaline phosphatase pulp Inorganic phosphate and calcium from the blood (Pisanti & Sciaky 1964) Precipitation of calcium phosphate
  • 30. Disadvantages of Ca(OH)2  Presence of tunnel defects in dentin barrier.  Extensive dentin formation.  High solubility in oral fluids.  Lack of adhesion & degradation after acid etching. Asgary et al, 2008, Cox et al, 1985, Pitt ford, Roberts 1991 30
  • 31. • Pulp capping with MTA is recommended for teeth with carious pulp exposures specially immature teeth with high potential for healing. Farsi N, et al 2006 • MTA is superior in terms of dentin bridge formation during the early healing process in human dental pulp. Min et al, 2008 • MTA seemed to heal the pulp tissue at a faster rate than CH cement in human teeth. Accornite et al, 2008 • MTA was clinically easier to use as a direct pulp capping agent and resulted in less pulpal inflammation and more predictable hard tissue barrier formation than Dycal. Nair PN et al, 2009 • It has excellent sealing ability. Torabinejad et al, 1993, 1994, Bates et al, 1996, Fischer et al, 1998, Wu et al, 1998. • Biocompatibility. Kettering & Torabinejad 1995, Torabinejad et al, 1997, 1998, Holland et al, 1999, Mitchell et al, 1999, Keiser et al, 2000 31
  • 32. Mechanism……………………… Calcium oxide present in MTA + tissue fluids calcium hydroxide calcite crystals attract fibronectin, which is responsible for cellular adhesion and differentiation (“Holland et al 1999”) Calcium ions released from MTA + phosphate in tissue fluid hydroxapatite
  • 33. initial deep caries and immature apices Pulpal exposure Five-minute application of 5.25% sodium hypochlorite hemostasis, on two 1.5- to 2.0-mm exposures 33
  • 34. Radiograph of molar with MTA after initial visit Radiograph taken at the 5.5-year recall appointment showing permanent restoration and evidence of complete root formation. (From Bogen G, Kim JS, Bakland LK: Direct pulp capping with mineral trioxide aggregate. An observational study. J Am Dent Assoc 139:305-315, 2008. 34
  • 35. • On the biological level, it is perfectly biocompatible & capable of inducing the apposition of reactionary 35 dentin by stimulating odontoblast activity & reparative dentin, by induction of cell differentiation . Laurent et al., 2008., Goldberg et al., 2009., Shayegan et al., 2010 • It is an effective dentin substitute that can be used as a coronal restoration material (for indirect pulp capping), but can also be placed in contact with the pulp. • Its faster setting time allows either immediate crown restoration, or to make it directly intraorally “functional” without fear of the material deteriorating. Tran et al., 2008 • Biodentine™ significantly increased TGF- β1 secretion from pulp cells independently of the contact surface compared to the increase by Ca(OH)2 & MTA. Laurent P, Camps J, About I: Int Endod J; May 2012, Vol. 45 Issue 5, p439-448.
  • 36. Clinical view Distal pulp horn involvement After removal of restoration Biodentine placement 36
  • 37. Post--‐operative clinical view Post‐operative X‐ray follow‐up image Ceramic onlay, final restoration after 2 months Post ‐operative X‐ray follow‐up image 37 Courtsey: Dr. Lucile Goupy
  • 38. • Antibacterial effect comparable to CH & superior to MTA Asgary S, Kamrani FA 2008 • Sealing ability similar to MTA Asgary S, Eghbal MJ, Parirokh M 2008 • Biologic response of pulp to MTA & CEM cement - similar in dogs’ teeth. Asgary S et al, 2008 • CEM cement provides an endogenous source of calcium & phosphate ions that accelerates hydroxyapatite (HA) crystal formation as a second-seal on its surface even in normal saline storage media. Aust Endod J 2009;35:147–52. • Set form of CEM cement is similar to dentin. J Endod 2009;35:243–50. 38
  • 39. • Hench – 1969 • Bioglass® 45S5  45wt% SiO2, 24.5wt% Na2O & CaO, and 6wt% P2O5. • React with aqueous solutions & produce a carbonated apatite layer. dentin • BAG can be the material of choice for pulp capping & periapical bone healing because it is biocompatible & has antibacterial property. Schepers et al, 1991 • BAG produce Less inflammation, dentin bridge formation & no internal resorption, necrosis or abscess compared to Ca(OH)2 Journal of Dentistry, Tehran University of Medical Sciences, Tehran, Iran (329007)
  • 40. • Enamel Matrix Derivative (EMD) is a rich Amelogenin & Amelin biomaterial that has been demonstrated to induce a reparative process similar to normal odontogenesis when placed in contact with pulp tissue. • MTA produced a better quality reparative hard tissue response with the adjunctive use of Emdogain, when compared with the use of calcium hydroxide. J Endod 35 , Pages 667-672, May 2011 40 Amelogenins form a matrix layer on the surface. Contact to cells of the healthy part of the dentin The cells secrete natural and specific cytokines and autokrine substances, which promote the required proliferation Adduction and proliferation of mesenchymal cells from the healthy part of the dentin Attraction and differentiation of odontoblasts, begin the formation of the matrix
  • 41. • Consists of Calcium silicates, Monobasic calcium phosphate, zirconium oxide, tantalum oxide • Hirschman et al compared Cytotoxicity of MTA-Angelus, Brasseler Endosequence Root Repair Putty (ERRP), Dycal & Ultra-blend Plus (UBP)-(light curable Ca(OH)2 & concluded that ERRP & UBP are less cytotoxic J Endod 2012 41
  • 42. • Light-cured resin-modified calcium silicate pulp protectant • Immediate placement & condensation. • TheraCal displayed higher calcium-releasing ability & lower solubility than either ProRoot MTA or Dycal. • The capability of TheraCal to be cured to a depth of 1.7 mm may avoid the risk of untimely dissolution. Int Endod J , 45: 571–579, June 2012. 42
  • 43. Bioactive molecules 1. Bone Sialoprotein (BSP) 2. Bone Morphogenetic Protein-7 (BMP-7), also termed Osteogenic Protein-1 (OP-1) “M. Goldberg et al - Adv Dent Res August 2001”
  • 44. 44 BSP & BMP implanted in the pulp recruitment of cells bearing an osteoblastic phenotype (i.e which differentiate into osteoblast like cells ) Produces a mineralizing extracellular matrix. Atubular Dentin dense layer.
  • 45. Miscellaneous • TGF-b1  Enhances reparative dentin formation Hu et al - J Endod. 1998 • Recombinant Insulin Like Growth Factor-I  rhIGF-I in rat molars resulted dentin bridge formation equal to dycal after 28 days Lovschall H, et al - J Endod. 2008 • Odontogenic Ameloblast Associated Protein (ODAM)  rODAM accelerates reactionary dentin formation close to the pulp exposure area, thereby preserving normal odontoblasts in the remaining pulp Yang IS et al - J Endod. 2010 45
  • 46. 46
  • 47. Def: “amputation of the affected or infected coronal portion of the dental pulp, preserving the vitality & function of all or part of the remaining radicular pulp”. AAPD guidelines 2014 47
  • 48. • Caries removal results in pulp exposure in a primary tooth with a normal pulp or reversible pulpitis or after a traumatic pulp exposure. • Radicular tissue is judged to be vital without suppuration, purulence, necrosis, or • Excessive hemorrhage that cannot be controlled by a damp cotton pellet after several minutes, • No radiographic signs of infection or pathologic re-sorption. 48
  • 49. According to Mejare: • Resorption exceeding >1/3rd of the root length • Nonrestorable tooth crown • Highly viscous, sluggish, or absent hemorrhage at the radicular canal orifices • Marked tenderness to percussion • Mobility with locally aggravated gingivitis associated with partial or total radicular pulp necrosis • Radiolucency in the furcal or periradicular areas • Persistent toothaches & coronal pus 49
  • 50. CLASSIFICATION  Amount of pulpal tissue involved  Cervical / Complete Pulpotomy  Partial pulpotomy [Cvek’s pulpotomy]  Type of medicament employed Grossman’s Endodontic Practice 12th Edition
  • 51. CLASSIFICATION Pedodontics – Shobha Tandon 2nd Edition 51 Types Other name Features Examples Devitalization Preservation Regeneration Mummification, cauterization Minimal devitalization, noninductive Inductive, reparative It is intended to destroy or mummify the vital tissue. This implies maintaining the maximum vital tissue,with no induction of reparative dentin. This has formation of dentin bridge. Single sitting Formocresol Electrosurgery Laser Two stage Gysi triopaste Easlick’s formaldehyde Paraform devitalizing paste ZnO Eugenol Glutaraldehyde Ferric sulphate Ca(OH)2 Bone morphogenic protein Mineral trioxide aggregate Enriched collagen Freezed dried bone Osteogenic protein
  • 52. Agents for pulpotomy Pharmacotherapeutic Formocresol Glutaraldehyde Calcium hydroxide Collagen Ferric sulfate CaPo4 cement Hydroxyapatite BMP 2 & 4 Freeze dried bone MTA CEM Biodentine Non-pharmacologic Electro surgery Lasers 52
  • 53. MTA & Formocresol JOE—Volume 34, Number 7, July 2008 53
  • 54. Ferric sulphate & Formocresol JOE—Volume 34, Number 7, July 2008 54
  • 55. CH & FC JOE—Volume 34, Number 7, July 2008 55
  • 56. Laser vs FC 56 Clinical (%) Radiograhic (%) Nd:YAG laser 97 94 FC 85 78 • The permanent successors of the laser-treated teeth erupted without any complications. J Endod, 2006: 32:404-7
  • 57. NaOCl vs FS Vargas et al, 2006 Duration Ferric sulphate NaOCl Paediatr Dent 2006, 28: 511-7 Clinical success Radiographic success Clinical success Radiographic success At 6 months 100% 68% 100% 91% At 12 months 85% 62% 100% 79% 57
  • 58. • Case reports showing successful pulpotomy with MTA 18 month 19 month 58 JADA, Vol. 137 May 2006
  • 59. Case report showing successful pulpotomy with CEM cement in permanent molar with irreversible pulpitis & condensing apical periodontitis: Saeed Asgary. J Conser Dent 2011, 14: 90-93 6 months 1 year 2 years 59
  • 60. 60

Editor's Notes

  1. Dr Norna Hall - scotland
  2. First method of capping exposed pulps, using gold foils was described by Pfaff in 1756.
  3. 1993 by Torabinejad Pitt Ford et al, 1996 - pulp capping – monkey teeth
  4. Tricalcium & Dicalcium silicate & Calcium carbonte ., Zirconium oxide Liquid – Calcium chloride with an admixture of modified polycarboxylate 30s – triturator 12 – 15mins - ST
  5. The protein in emdogain is of porcine origin with very high homogeneity to human amelogenins