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Vital Pulp Therapy

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Page 1: Vital Pulp Therapy

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Greatest challenges to the integrity

of the developing tooth

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Primary goal

Maintain pulp vitality

Normal tooth development

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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

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Key responses of the dentin-pulp to caries / injury

Tertiary dentin 5

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Reactionary dentinogenesis

Caries

Odontoblasts

Dentin

Tertiary, reactionary dentin laid

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Reparative dentinogenesis

Tertiary,

reparative dentin

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• RDT is a key determinant of pulp survival after cavity preparation & avoiding pulp

exposure has been considered advantageous.Int Endod J 41:389, 2008.

Remaining Dentinal Thickness/ Effective Depth

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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

Endodontics : Ingle 5th edi10

Determining the pulpal status of cariously involved teeth involves the following:

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- Type of injury

- age of the pt

- size & location of the pulp exposure

- bacterial contamination

- pulp capping material &

- quality of the final restoration

The outcome of VPT depends on:

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Vital pulp therapy

Indirect pulp capping

Direct pulp capping

Pulpotomy

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• 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.

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 :

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• 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

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• 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 roots16

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• Hard setting Ca(OH)2

• ZOE

• GIC (Glass ionomer caries control approach)

• Resin modified glass ionomer

• Bonded composite

• MTA

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• IPC studies show success rates of 90% or greater over time with differing

techniques and medicaments.

J Endod Vol 34, No 7S, July 2008

IPT medicaments Success

(%)

Time (mo) Sample

(N)

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

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• 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

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• Two appointment technique

• One appointment technique

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• 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.

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Guideline on Restorative Dentistry

Recommendations

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.

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American Academy of Pediatric Dentistry (AAPD) & American Association of Endodontists (AAE)

2014

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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.

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1. Small pin point mechanical exposures of diameter < 1.0mm

2. Pulp exposed without previous symptoms of pulpitis.

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(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.

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• 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

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Calcium Hydroxide - gold standard

Hermann (1920) - introduced the use of

CaOH2 as a clinical procedure to stimulate pulp

healing and dentin bridge formation.

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Mechanism:

enzyme alkaline

phosphatase

CH – high alkaline medium

Coagulation necrosis of the surface of the

pulp

Inorganic phosphate and calcium from the

blood (Pisanti & Sciaky 1964)

Precipitation of calcium

phosphate

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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

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• 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

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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

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initial deep caries and immature apices

Five-minute application of 5.25% sodium hypochlorite

hemostasis, on two 1.5- to 2.0-mm exposures

Pulpal exposure

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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

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• On the biological level, it is perfectly biocompatible & capable of inducing the apposition of reactionary

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.

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Clinical view Distal pulp horn involvement

After removal of restoration Biodentine placement

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Post--‐operative clinical view Post‐operative X‐ray follow‐up image

Ceramic onlay, final restoration

after 2 monthsPost ‐operative X‐ray follow‐up image

Courtsey: Dr. Lucile Goupy

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• 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.

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• Hench – 1969

• Bioglass® 45S5 45wt% SiO2, 24.5wt% Na2O & CaO, and 6wt% P2O5.

• React with aqueous solutions & produce a carbonated apatite layer.

• 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 (2007)39

dentin

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• 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

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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 autokrinesubstances, 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

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• 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

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• 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.

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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”

Bioactive molecules

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BSP & BMP

implanted in the pulp

recruitment of cells bearing an osteoblastic phenotype

(i.e which differentiate into osteoblast like cells )

Atubular Dentin dense layer.

Produces a mineralizing extracellular matrix.

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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 daysLovschall 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

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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

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• 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.

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• 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

According to Mejare:

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CLASSIFICATION

Amount of pulpal tissue involved

Cervical / Complete Pulpotomy

Partial pulpotomy [Cvek’s pulpotomy]

Type of medicament employed

Grossman’s Endodontic Practice 12th Edition

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CLASSIFICATION

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Pedodontics – Shobha Tandon 2nd Edition

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 sittingFormocresolElectrosurgeryLaser Two stageGysi triopasteEaslick’s formaldehydeParaform devitalizing paste

ZnO EugenolGlutaraldehydeFerric sulphate

Ca(OH)2 Bone morphogenic proteinMineral trioxide aggregateEnriched collagenFreezed dried bone Osteogenic protein

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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

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MTA & Formocresol

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JOE—Volume 34, Number 7, July 2008

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Ferric sulphate & Formocresol

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JOE—Volume 34, Number 7, July 2008

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CH & FC

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JOE—Volume 34, Number 7, July 2008

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Laser vs FC

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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

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NaOCl vs FS

Vargas et al, 2006

Paediatr Dent 2006, 28: 511-7

Duration Ferric sulphate NaOCl

Clinical

success

Radiographic

success

Clinical

success

Radiographic

success

At 6 months 100% 68% 100% 91%

At 12 months 85% 62% 100% 79%

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• Case reports showing successful pulpotomy with MTA

JADA, Vol. 137 May 2006

18 month

19 month

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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

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