Key Points
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Mineral trioxide aggregate (MTA) was assessed in pulpotomised primary molars.
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The clinical and radiographic success rate of MTA was recorded at 24 months follow-up.
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This clinical trial study showed the success of white MTA in primary molars.
Abstract
Purpose The aim of this study was to compare the effect of white mineral trioxide aggregate (MTA) to that of formocresol (FC) as pulp dressing agents in pulpotomised primary molars.
Methods In this clinical trial study, 60 lower second primary molars of 46 children were treated by a conventional pulpotomy technique. The teeth were randomly assigned to the MTA (experimental) and FC (control) groups by random numbered table. Following removal of the coronal pulp and haemostasis, the pulp stumps were covered with an MTA paste in the experimental group. In the control group, FC was placed with a cotton pellet over the pulp stumps. The teeth of both groups were restored with stainless steel crowns. Children arrived for clinical and radiographic follow-up evaluation after 6, 12 and 24 months.
Results The treated teeth in FC group (n = 18) were clinically and radiographically successful after 24 months. The radiographic follow-up evaluation revealed one failure (furcation involvement) in 18 molars treated with MTA after 24 months. The treated teeth in MTA group were clinically successful 24 months postoperatively. Pulp canal obliteration was observed in one of the teeth treated with MTA and four of the teeth treated with FC.
Conclusion MTA could be used as a safe medicament for pulpotomy in cariously exposed primary molars and could be a substitute for FC.
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Introduction
Recent progress in understanding the molecular and cellular changes during tooth development and how they are mimicked during tissue repair, offers the opportunity to assess the biologic validity of the various vital pulp treatments. Under this light, indirect pulp treatment can be an acceptable procedure for primary teeth with reversible pulp inflammation, provided that this diagnosis is based on a good history, a proper clinical and radiographic examination, and the tooth had been sealed with a leakage-free restoration.1 Direct pulp capping of carious exposures in young permanent teeth is an accepted procedure, but in primary teeth it is contraindicated.2 In younger children, pulpotomy is indicated for any carious or traumatic pulp exposures in primary teeth.2 Formocresol (FC) has been the most popular pulp dressing material for pulpotomised primary molars for many years but, due to its deleterious effect,3,4 the use of FC is decreasing considerably worldwide. Ferric sulphate has been proposed as a substitute for FC, and its success rates are comparable to those of FC.5,6,7
More recently, considerably better results have been obtained with MTA (mineral trioxide aggregate).8,9,10 MTA was introduced to endodontics by Torabinejad et al. in 1993.11 MTA is marketed in grey and white preparations. In recent years, the use of the white (tooth-coloured) preparation has become more popular in incisor teeth due to the discolouration using grey MTA.12,13,14 MTA is a powder that consists of fine hydrophilic particles that in the presence of water, or moisture, forms a colloidal gel that solidifies to form hard cement within approximately four hours. The principal components of the grey-coloured formula are tricalcium oxide, tricalcium silicate, bismuth oxide, dicalcium silicate, tricalcium aluminate, tetracalcium aluminoferrite and calcium sulfate dihydrate.15,16,17,18 The more aesthetic white-coloured preparation lacks the tetracalcium aluminoferrite.19,20 Lately, MTA has been used as a pulpotomy medicament in primary molars and it was found to be a successful material.13,21,22
The objective of this study was to clinically and radiographically evaluate the effects of tooth-coloured (white) MTA as a pulp dressing agent in pulpotomised lower second primary molars for 24 months and compare them to those of FC.
Methods and materials
The procedure and its possible discomfort and benefits were explained fully to the parents of the children involved and their written consent was obtained prior to the investigation. Also, the approval of the Undersecretary for Research at Zahedan University of Medical Sciences was obtained prior to the study.
Forty-six Iranian children (29 boys,17 girls) were selected for clinical and radiographic study from patients attending the clinic of the Paediatric Dentistry Department, Faculty of Dentistry, Zahedan University of Medical Sciences. Their ages ranged between 5-7 years, with a mean age of 6.08. The children had no systemic diseases. The suitability of the teeth for pulpotomy was assessed by the author who also performed the procedures. The criteria for selection of the teeth to be included in the study were: 1) symptomless exposure of vital pulp by caries; 2) no clinical or radiographic evidence of pulp degeneration, such as excessive bleeding from the root canal, internal root resorption, interradicular and/or periapical bone destruction, swelling or sinus tract; and 3) the possibility of proper restoration of the teeth.
Sixty lower second primary molars were treated by a conventional pulpotomy technique. The teeth were randomly assigned to either the control or experimental group (30 teeth each) by random numbered table. In case a child had two molars needing pulpotomy, the second tooth was assigned to the alternative group.
All molars were treated with inferior alveolar nerve block anaesthesia and rubber dam isolation. After caries removal, coronal access was obtained with a 330 high-speed bur with water spray to expose the pulp chamber. Following removal of the coronal pulp with a round bur and haemostasis, the pulp stumps in the experimental group were covered with an MTA paste, obtained by mixing MTA powder with distilled water in a 3:1 powder/water ratio, according to the manufacturer's recommendations. The MTA used in this study was tooth-coloured (white) MTA (Dentsply, Tulsa Dental). The choice of white MTA was made purely because it was the newest product. In this group a cotton pellet moistened with normal saline was placed over the MTA paste and the tooth was temporarily restored using fast-setting zinc oxide-eugenol (ZOE), because the MTA hardened within approximately four hours.
In the control group, a cotton pellet moistened with 1:5 diluted FC (Buckleys) was placed for five minutes on the pulp stumps and then the pulps were covered with zinc oxide-eugenol (ZOE) paste. In both groups, teeth were restored with stainless steel crown (in MTA group after 24 hours and in FC group immediately).
The children were recalled for clinical and radiographic examination after 6, 12 and 24 months. When a patient did not respond or cancelled an appointment, further attempts were made to contact the parents and a follow-up examination was rescheduled. The children were examined clinically and radiographically at follow-up by the author who was blind to which treatment group the subject belonged. The dental assistant recorded the name, code of file, residence and telephone number of patients on a separate follow-up index card for 6, 12 and 24 months.
Teeth were scored as clinical successes if they had no pain symptoms, tenderness to percussion, swelling, fistulation or pathologic mobility. Teeth were scored as radiographic successes if they showed no evidence of radicular radiolucency, internal or external root resorption, or periodontal ligament space widening. The treatment was regarded as a failure when one or more of the following signs were present: internal root resorption, furcation radiolucency, periapical bone destruction, pain, swelling, or sinus tract. Pulp canal obliteration (PCO) was not regarded as a failure.
The data were analysed to assess the success rate of the treatment at the various follow-up periods. The differences were statistically analysed using the Fisher's exact test.
Results
Six months follow-up: 43 children with 56 teeth arrived for postoperative evaluation. All the treated teeth in the two groups (FC = 27, MTA = 29) were clinically and radiographically successful.
Twelve months follow-up: 41 children with 53 teeth arrived for clinical and radiographic examination. The treated teeth in the FC group (n = 24) were clinically and radiographically successful. The treated teeth in the MTA group (n = 29) were clinically successful but the radiographic follow-up evaluation revealed one failure, furcation involvement, in molars treated with MTA (Fig. 1).
Twenty-four months follow-up: 27 children with 36 teeth arrived for postoperative evaluation. The treated teeth in the FC group (n = 18) were clinically and radiographically successful (Fig. 2). The treated teeth in the MTA group (n = 18) were clinically successful. Figure 3 shows the radiographic success in a molar treated with MTA. The radiographic follow-up evaluation revealed one failure, furcation involvement, in another of the molars treated with MTA (Fig. 4).
All the teeth were scored as clinical successes at the 6, 12 and 24-month postoperative evaluations. The radiographic assessments of the teeth are shown in Table 1.
Pulp canal obliteration was observed in one of the teeth treated with MTA and four of the teeth treated with FC. The time of detection of obliteration was 12 months after treatment.
Discussion
This study examined the clinical and radiographic success rate of pulpotomies with MTA in comparison with FC and showed the samples treated with MTA had the same success rate as those treated with FC.
The retention of pulpally involved primary teeth in a healthy state until the time of normal exfoliation remains one of the challenges for paedodontists. Concerns have been raised about the toxicity and potential carcinogenicity of the popular pulpotomy medicament (FC) and alternatives have been proposed to maintain partial pulp vitality.
MTA has been proposed as a potential medicament for various pulpal procedures in permanent teeth, eg pulp capping, apexification, repair of root perforations etc, and has had successful results.20,21,22,23,24 With due attention to the biocompatibility and biological seal of MTA, several studies have been performed to evaluate its efficacy as a pulpotomy medicament in primary molars.8,9,10,13,21
Eidelman et al.8 showed MTA pulpotomies in primary molars that were followed up for 6-30 months were clinically and radiographically successful. In the studies of Naik9 and Maroto et al.,13 the clinical and radiographic evaluations were done at six months after pulpotomy in primary molars. Their studies also showed that MTA was a successful material. Agamy et al.10 compared the success of grey MTA, white MTA and FC as pulp dressings in pulpotomised primary teeth using clinical, radiographic and histologic examinations. They concluded that grey MTA appears to be superior to white MTA and FC in pulpotomised primary teeth and confirmed that the biocompatibility of MTA was similar to that found in other in vivo and in vitro studies.23,26,27
The results of this study showed that all the treated teeth in the MTA and FC groups were clinically successful. Also, the radiographic success of the FC group was complete within the 6 to 24 months follow-up time. The radiographic evaluation revealed one failure at 12 months postoperatively and one failure at 24 months postoperatively in molars treated with white MTA. The present study did not see the failure rate in white MTA pulpotomies that Agamy et al.10 found. One reason may be that the present study treated second primary molars only, while the above-mentioned studies treated all primary molars. Vij28 found that first primary molar pulpotomies had a 61% success rate while the success rate for second molars was 83%.
Farsi et al.21 reported a significant difference between the two groups (MTA and FC pulpotomies in primary molars) after 24 months of radiographic evaluation, but the results of this study were not statistically significant and agree with the study of Holan et al.22 In their study, MTA showed a higher (though not statistically significant) long-term clinical and radiographic success rate than formocresol.22
In spite of the similarity of success rates of FC and MTA in this study, one clinical disadvantage of MTA compared to FC is the fact that the tooth has to be restored after 24 hours to allow time for the MTA to set. In addition, MTA is more expensive and more difficult to prepare than FC.
In the present study there was a high drop-out rate after 24 months (12 out of 30 teeth in two groups) and it is possible that the some of failures have not returned. Therefore further studies with a larger sample size and longer follow-up periods are recommended.
Pulp canal obliteration has been reported as a common radiographic finding in pulpotomised teeth treated with FC,8 MTA8,10 and ferric sulfate.29 In the present study pulp canal obliteration was present in the two groups. The obliteration is the result of odontoblastic activity and suggests that the tooth is retaining some degree of vitality30 and therefore was not regarded as failure.
Conclusion
Based on the present study, MTA could be used as a safe medicament for pulpotomy in cariously exposed primary teeth and could be a substitute for FC.
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Noorollahian, H. Comparison of mineral trioxide aggregate and formocresol as pulp medicaments for pulpotomies in primary molars. Br Dent J 204, E20 (2008). https://doi.org/10.1038/sj.bdj.2008.319
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DOI: https://doi.org/10.1038/sj.bdj.2008.319
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