Literature DB >> 19148409

Pulpotomies with Portland cement in human primary molars.

Taísa Regina Conti1, Vivien Thiemy Sakai, Ana Paula Camolese Fornetti, Ana Beatriz Silveira Moretti, Thais Marchini Oliveira, Natalino Lourenço Neto, Maria Aparecida Andrade Moreira Machado, Ruy Cesar Camargo Abdo.   

Abstract

Two clinical cases in which Portland cement (PC) was applied as a medicament after pulpotomy of mandibular primary molars in children are presented. Pulpotomy using PC was carried out in two mandibular first molars and one mandibular second molar, which were further followed-up. At the 3, 6 and 12-month follow-up appointments, clinical and radiographic examinations of the pulpotomized teeth and their periradicular area revealed that the treatments were successful in maintaining the teeth asymptomatic and preserving pulpal vitality. Additionally, the formation of a dentin bridge immediately below the PC could be observed in the three molars treated. PC may be considered as an effective alternative for primary molar pulpotomies, at least in a short-term period. Randomized clinical trials with human teeth are required in order to determine the suitability of PC before unlimited clinical use can be recommended.

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Year:  2009        PMID: 19148409      PMCID: PMC4327617          DOI: 10.1590/s1678-77572009000100013

Source DB:  PubMed          Journal:  J Appl Oral Sci        ISSN: 1678-7757            Impact factor:   2.698


INTRODUCTION

Pulpotomy is the most widely accepted clinical procedure for treating primary teeth with inflammation of the coronal pulp caused by caries with no involvement of the radicular pulp. This technique consists of removing the coronal pulp and healing the radicular pulp with a medicament. The purpose is to remove the bacterial infection leaving the treated tooth asymptomatic until its exfoliation13,24. Medicaments applied to radicular pulp tissue after pulpotomy have included formocresol1,13, ferric sulphate13, calcium hydroxide30, and mineral trioxide aggregate (MTA)1,2,4,12,22,23,28. Recently, great interest has been focused on the evolution of Portland cement (PC) as an alternative to MTA, and several studies have compared both materials3,6,8,9,11,15–17,31 PC differs from MTA by the absence of bismuth ions5,11,18,26 and the presence of potassium ions25. Both materials have comparable antibacterial activity11 and almost identical properties macroscopically, microscopically and by X-ray diffraction analysis16,26,31. It has also been shown that PC and MTA have similar effect on pulpal cells when used for direct pulp capping in rat teeth31. Holland, et al.16 studied the rat subcutaneous connective tissue response to implanted dentin tubes filled with MTA, PC and calcium hydroxide and found very similar mechanisms of action. In addition, both MTA and PC allowed for dentin bridge formation after pulpotomy was performed in dogs15. Finally, Min, et al.21 observed that PC allowed the expression of mRNAs of a dentin-specific protein and a noncollagenous protein involved in mineralization in cultured human pulp cells. Taking into account the low cost and apparently similar properties of PC in comparison to MTA, it is reasonable to consider PC as a possible substitute for MTA in endodontic applications9,10,20,25,31. Therefore, this paper presents two clinical cases in which PC was applied as a medicament after pulpotomy of mandibular primary molars in children.

CASE REPORTS

A 7-year old boy and a 6-year old girl were referred to our institution with a request for dental care because of the presence of caries lesion. They had no systemic pathology or known allergies to latex, topical or local anesthetics or to the compounds from which PC is made. The following findings were observed in mandibular primary molars: need for a pulpotomy treatment due to caries; no previous treatment; no signs of radicular pulp degeneration (abscesses of associated fistulous tracts); no radiographic signs of furcation involvement, internal or external pathological root resorption, or pathological thickening of the periodontal membrane; no increased mobility; two thirds or more of root length and possibility of restoration using resin modified glass ionomer cement19 (Figures 1a and 2a).
FIGURE 1A

Preoperative periapical radiograph of the mandibular right primary first molar of a 7-year old boy, which presented an extensive caries lesion, more than two thirds of root length and no signs of periapical lesion

FIGURE 2A

Preoperative periapical radiograph of the mandibular left primary molars of a 6-year old girl, which presented extensive caries lesions, two thirds or more of root length, and no signs of periapical lesion. Agenesis of the mandibular left permanent second premolar was observed

The pulpotomy procedure using PC was carried out on two mandibular first molars and one mandibular second molar. Although one could consider a risk the use PC in humans, it is worth mentioning that its use was assessed by Brazilian Health Ministry and further approved by the Research Ethics Committee of the Bauru School of Dentistry, University of São Paulo (Protocol # 34/2005), thus validating the execution of the present clinical cases in human primary teeth. In both cases, rubber dam isolation was used. Under local anesthesia, the teeth were excavated using handpiece with a bud bur. The opening of the pulp chambers was conducted with carbide bur, followed by irrigation with saline solution. The coronal pulp tissues were removed manually with an excavator. Drying and controlled bleeding of the remaining pulp tissues were obtained using slight pressure with a sterile cotton pellet, and then PC (Votorantim-Cimentos, São Paulo, SP, Brazil) was used. 0.16 g of PC was previously sterilized with ethylene oxide, mixed with sterile water to produce a homogenous paste and applied into the pulp chambers with a spatula. A layer of reinforced zinc oxide-eugenol (IRM®; Dentsply Ind. e Com. Ltda, Petrópolis, RJ, Brazil) was placed prior to restoration with resin modified glass ionomer cement (Vitremer®, 3M/ESPE, St. Paul, MN, USA). Immediate postoperative radiographs were taken. Periodic follow-up examinations were carried out 3 (Figures 1b and 2b), 6 (Figures 1c and 2c) and 12 months (Figures 1d and 2d) after the end of the treatment. Each checkup involved a clinical and radiographic examination of the pulpotomized teeth and their periradicular area, revealing that the treatments were successful in maintaining the teeth asymptomatic and preserving pulpal vitality. Additionally, the radiographic examinations revealed formation of a bridge, presumably dentin, immediately below the PC in the three molars treated.
FIGURE 1B

3-month follow-up periapical radiograph suggesting the initial formation of a dentin bridge immediately below the Portland cement in the mesial root (arrow) and absence of periapical lesion in the pulpotomized mandibular right primary first molar

FIGURE 2B

3-month follow-up periapical radiograph suggesting the initial formation of a dentin bridge immediately below the Portland cement in the distal root (arrow) of the pulpotomized mandibular left second molar and absence of periapical lesion in both pulpotomized mandibular left primary molars

FIGURE 1C

6-month follow-up periapical radiograph suggesting the presence of the dentin bridge immediately below the Portland cement in the mesial root (arrow) of the pulpotomized mandibular right primary first molar

FIGURE 2C

6-month follow-up periapical radiograph suggesting the presence of the dentin bridge immediately the Portland cement in the distal root (arrow) of the pulpotomized mandibular left second molar

FIGURE 1D

12-month follow-up periapical radiograph suggesting the presence of the dentin bridge immediately below the Portland cement in the mesial root (arrow) of the pulpotomized mandibular right primary first molar

FIGURE 2D

12-month follow-up periapical radiograph suggesting the initial radicular pulp obliteration of the mandibular right primary first molar

The patients will be monitored quarterly in order to follow-up the pulpotomized molars and the eruption of all permanent teeth.

DISCUSSION

Several studies have reported excellent results when using MTA in endodontic treatments1,2,12,19,20,22,23,28,29. The factor responsible for the beneficial effects in MTA is also found in PC27. This has resulted in a significant body of research that shows that PC appears to be a useful substitute for MTA9,10,20,25,27,31. However, only four studies reported the use of PC in conservative pulp therapy with considerable success in rats31 and dogs15,17,20. In humans, there is only one work showing the use of PC in order to create an apical plug in the root of an immature tooth7. To the best of our knowledge, the case reports presented here is the first to describe the use of PC as a medicament after pulpotomy in human primary teeth. After 3-month follow-up, a hard tissue barrier could be observed immediately below the PC, which was confirmed at the 6-month follow-up appointment. The ability of this material to induce the formation of a dentin bridge may be due to its mechanisms of action. PC has calcium oxide that forms calcium hydroxide when mixed with water. The reaction of the calcium from calcium hydroxide with the carbon dioxide from the pulp tissue produces calcite crystals. Then, a rich extracellular network of fibronectin in close contact with these crystals can be observed, strongly supporting the role of calcite crystals and fibronectin as an initiating step in the formation of a hard tissue barrier15. Moreover, PC has an excellent sealing ability and fast setting, thus preventing the diffusion of the material into the tissues, and reducing microleakage during the pulp healing period20. Danesh, et al.6 showed that MTA displayed superior material properties than PC, which was significantly more soluble, reached lower microhardness values and was less radiopaque. The lack of radiopacity in pure PC is due to the absence of bismuth, a chemically inert radiopacifier, in its composition5. However, this feature does not compromise the execution of pulpotomy procedures with PC and their follow-up assessments, which is untrue when this material is used for root-end fillings. In these situations, a radiopacifier is necessary to enable the peri- and postoperative assessment of the cement placement reaching the end of the root. A major concern regarding the use of water-based cements is the amount of leachable arsenic and lead present in the material. Arsenic and lead are impurities of limestone that is used in the manufacture of PC17. Duarte, et al.10 showed that the concentration of arsenic is low in PC and closely similar to that present in MTA, demonstrating no contraindication of the use of that material in clinical practice concerning the presence of this chemical element. However, no study has compared the lead content in these cements17. In the cases presented here, the use of a stainless steel crown to restore the teeth was considered. Even though, a provisional and faster restoration with glass ionomer cement was chosen. Glass ionomer cement has good sealing properties and it is easy to handle14,22. Adhesion properties of this material impart adequate retention even if mechanical undercuts are absent. Coverage of exposed dentin and sharp margins with glass ionomer cement to provide patient comfort is accomplished with minimal chair time14,22. It is important that the absence of evidence for glass ionomer cement should not be misinterpreted as evidence for its lack of efficacy. The present cases revealed that PC may be considered as an effective and economic alternative medicament to formocresol and mineral trioxide aggregate for primary molar pulpotomies since the treated teeth were retained asymptomatic in the oral cavity and dentin barriers could be observed immediately below the material. Although our results are very encouraging, randomized clinical trials with human teeth need to be conducted in order to determine the suitability of PC before unlimited clinical use can be recommended.
  29 in total

1.  Reaction of rat connective tissue to implanted dentin tube filled with mineral trioxide aggregate, Portland cement or calcium hydroxide.

Authors:  R Holland; V de Souza; M J Nery; I M Faraco Júnior; P F Bernabé; J A Otoboni Filho; E Dezan Júnior
Journal:  Braz Dent J       Date:  2001

2.  Mineral trioxide aggregate as a pulpotomy agent in primary molars: an in vivo study.

Authors:  S Naik; A H Hegde
Journal:  J Indian Soc Pedod Prev Dent       Date:  2005-03

3.  Comparison of the physical and mechanical properties of MTA and portland cement.

Authors:  Intekhab Islam; Hui Kheng Chng; Adrian U Jin Yap
Journal:  J Endod       Date:  2006-03       Impact factor: 4.171

4.  A prospective clinical study of mineral trioxide aggregate for partial pulpotomy in cariously exposed permanent teeth.

Authors:  Kefah Mahmood Barrieshi-Nusair; Muawia Abdulla Qudeimat
Journal:  J Endod       Date:  2006-06-23       Impact factor: 4.171

5.  Chemical analysis of powder and set forms of Portland cement, gray ProRoot MTA, white ProRoot MTA, and gray MTA-Angelus.

Authors:  Jin-Seon Song; Francis K Mante; William J Romanow; Syngcuk Kim
Journal:  Oral Surg Oral Med Oral Pathol Oral Radiol Endod       Date:  2006-04-21

6.  Effect of bismuth oxide radioopacifier content on the material properties of an endodontic Portland cement-based (MTA-like) system.

Authors:  Kristian S Coomaraswamy; Philip J Lumley; Michael P Hofmann
Journal:  J Endod       Date:  2007-03       Impact factor: 4.171

7.  Mineral trioxide aggregate pulpotomies: a case series outcomes assessment.

Authors:  David E Witherspoon; Joel C Small; Gary Z Harris
Journal:  J Am Dent Assoc       Date:  2006-05       Impact factor: 3.634

8.  Sealing ability of a mineral trioxide aggregate when used as a root end filling material.

Authors:  M Torabinejad; T F Watson; T R Pitt Ford
Journal:  J Endod       Date:  1993-12       Impact factor: 4.171

9.  Cytotoxicity of MTA and Portland cement on human ECV 304 endothelial cells.

Authors:  G De Deus; R Ximenes; E D Gurgel-Filho; M C Plotkowski; T Coutinho-Filho
Journal:  Int Endod J       Date:  2005-09       Impact factor: 5.264

10.  Current concepts in vital primary pulp therapy.

Authors:  A B Fuks
Journal:  Eur J Paediatr Dent       Date:  2002-09       Impact factor: 2.231

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  7 in total

1.  Clinical, radiographic and histologic analysis of the effects of pulp capping materials used in pulpotomies of human primary teeth.

Authors:  T M Oliveira; A B S Moretti; V T Sakai; N Lourenço Neto; C F Santos; M A A M Machado; R C C Abdo
Journal:  Eur Arch Paediatr Dent       Date:  2013-04-03

2.  Comparison of mineral trioxide aggregate and diluted formocresol in pulpotomized human primary molars: 42-month follow-up and survival analysis.

Authors:  Sarah E Mettlach; Cameron M Zealand; Tatiana M Botero; James R Boynton; Robert F Majewski; Jan ChingChun Hu
Journal:  Pediatr Dent       Date:  2013 May-Jun       Impact factor: 1.874

3.  Healing of apical rarefaction of three nonvital open apex anterior teeth using a white portland cement apical plug.

Authors:  Amitabha Chakraborty; Bibhas Dey; Reema Dhar; Prabir Sardar
Journal:  Contemp Clin Dent       Date:  2012-09

Review 4.  Cytotoxicity and biocompatibility of direct and indirect pulp capping materials.

Authors:  Karin Cristina da Silva Modena; Leslie Caroll Casas-Apayco; Maria Teresa Atta; Carlos Alberto de Souza Costa; Josimeri Hebling; Carla Renata Sipert; Maria Fidela de Lima Navarro; Carlos Ferreira Santos
Journal:  J Appl Oral Sci       Date:  2009 Nov-Dec       Impact factor: 2.698

5.  Portland cement use in dental root perforations: a long term followup.

Authors:  Alvaro Henrique Borges; Matheus Coelho Bandeca; Mateus Rodrigues Tonetto; Luis Augusto Faitaroni; Elibel Reginna de Siqueira Carvalho; Juliane Maria Guerreiro-Tanomaru; Mário Tanomaru Filho
Journal:  Case Rep Dent       Date:  2014-03-03

Review 6.  A review on vital pulp therapy in primary teeth.

Authors:  Iman Parisay; Jamileh Ghoddusi; Maryam Forghani
Journal:  Iran Endod J       Date:  2014-12-24

7.  Clinical and Radiographic Evaluations of Biodentine™ Pulpotomies in Mature Primary Molars (Stage 2).

Authors:  Hitaf Nasrallah; Balsam El Noueiri; Charles Pilipili; Fouad Ayoub
Journal:  Int J Clin Pediatr Dent       Date:  2018 Nov-Dec
  7 in total

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