RESEARCH ARTICLE


https://doi.org/10.5005/jp-journals-10005-2120
International Journal of Clinical Pediatric Dentistry
Volume 15 | Special Issue 1 | Year 2022

Treatment Outcomes of Pulpotomy with Propolis in Comparison with MTA in Human Primary Molars: A 24-month Follow-up Randomized Controlled Trial


Kakarla Sri RojaRamya1, Rayala Chandrasekhar2, KS Uloopi3, C Vinay4

1-4Department of Pedodontics and Preventive Dentistry, Vishnu Dental College, Bhimavaram, Andhra Pradesh, India

Corresponding Author: Kakarla Sri RojaRamya, Department of Pedodontics and Preventive Dentistry, Vishnu Dental College, Bhimavaram, Andhra Pradesh, India, Phone: +91 8985774540, e-mail: rojachowdary28@gmail.com

ABSTRACT

Aim and objective: To evaluate the clinical efficacy of propolis as pulpotomy medicament in human primary molars.

Materials and methods: This randomized controlled trial is a two-arm, parallel group study with blinded outcome assessment. The study included a total of 60 primary molars that require pulpotomy treatment in 4- 8-year old children. Teeth were assigned to two groups randomly: Propolis (Test group); Mineral trioxide aggregate (MTA) (Control group). All the pulpotomized teeth were given stainless steel crowns and the teeth were evaluated clinically and radiographically at 6, 12, and 24 months to grade them as either success or failure. Chi-square test was employed to analyze the data.

Results: Success rates of pulpotomy with propolis and MTA were 80% and 93.1% respectively at 24 months of follow-up interval. Propolis has shown success rates of 90% and 80% at 6- and 12-month follow-up, while MTA has shown a consistent success rate of 93.1% at all the follow-up intervals. The difference in success rate between the groups at all the time intervals is statistically nonsignificant.

Conclusion: Propolis has demonstrated a clinically acceptable success rate comparable to MTA as pulpotomy medicament in primary teeth.

Clinical significance: Biocompatible materials with regenerative potential have drawn the momentum in vital pulp therapy. In this regard, MTA has been emerged as most successful material, but its high cost has limited its use. Hence, there is an absolute need of cost-effective pulpotomy material with regenerative potential. This study provides an evidence that propolis has clinically acceptable success rate as pulpotomy medicament. Considering its low cost and ready availability, it can be recommended as a cost-effective alternative for primary teeth pulpotomy.

How to cite this article: RojaRamya KS, Chandrasekhar R, Uloopi KS, et al. Treatment Outcomes of Pulpotomy with Propolis in Comparison with MTA in Human Primary Molars: A 24-month Follow-up Randomized Controlled Trial. Int J Clin Pediatr Dent 2022;15(S-1):S3-S7.

Source of support: Nil

Conflict of interest: None

Keywords: MTA, Propolis, Primary teeth, Pulpotomy, Randomized controlled trial, Vital pulp therapy

INTRODUCTION

In pediatric dentistry, pulpal infection is the most commonly encountered treatment challenge. Pulpotomy is the indicated treatment if infection is confined to the coronal pulp tissue and radicular pulp is healthy. This procedure maintains the radicular pulp’s vitality and allows the tooth to be retained in the arch. The outcome of pulpotomy is mostly determined by the medicament used.

For the past 70 years, formocresol has been the most preferred pulpotomy medicament for primary molars. However, due to its undesirable consequences such as mutagenicity and carcinogenicity, the usage of formocresol has been questioned.1 Owing to these concerns, various other medicaments such as glutaraldehyde, ferric sulfate, mineral trioxide aggregate as well as methods such as electrosurgery and laser were tested and have shown a varied clinical success.

The paradigm shift from mere preservation to regeneration in endodontics has promoted MTA as an alternative vital pulp therapy medicament. MTA has been successfully used for permanent tooth apexogenesis and apexification treatments, root perforation repairs, and other procedures. MTA is also being popularly used in primary teeth as pulpotomy medicament and has shown promising results. However, high cost and poor handling characteristics have limited its use.

Nowadays, use of natural plant products for therapeutic purposes, the phytotherapy, is gaining popularity. Propolis is a bee hive product that honey bees produce from the substances gathered from tree buds, leaf buds, and plant resinous secretions. It has potent antibacterial,2 anti-inflammatory,3 and tissue-regenerative properties.4,5 Based on the literature evidence of these beneficial properties, we tested propolis as pulpotomy medicament in comparison with MTA in human primary molars.

MATERIALS AND METHODS

Study Design

This randomized controlled trial is a two-arm, parallel group study with blinded outcome assessment and 1:1 allocation. The study was approved by Institutional Ethical Committee (VDC/IEC/2014-17) and is enlisted in Clinical trials registry-India (CTRI/2018/04/013352). The experimental protocol adhered to the ethical standards of the human experimentation, Declaration of Helsinki.

Participants Details

The study comprised 60 primary molars indicated for pulpotomy in 4- 8-year old children attending out-patient department of Pediatric Dentistry and the participants were followed up for 24 months.

Eligibility Criteria

Primary molars with deep caries lesion without spontaneous or persistent pain, teeth with at least two-thirds of root length intact, and restorable with stainless steel crowns in children who are nonallergic to propolis were included in the study. Teeth exhibiting the signs and symptoms of chronic infection such as sinus tract, swelling and mobility, teeth showing radiographic evidence of pathologic root resorption, inter-radicular bone loss, periapical pathology, and calcifications in the canal were excluded.

Primary Outcome

The success of propolis and MTA pulpotomies in primary molars at 6, 12, and 24 months of follow-up is the primary outcome.

Sample Size

Based on the previous studies, setting the significance level at 5%, power 80%, and difference 25%, the required sample size was calculated as 24 per group by substituting in the formula n = [(Zα/2 + Zβ)2×{(p1 (1-p1)) + (p2 (1-p2))}] /(p1 - p2)2,6,7 However, considering the sample dropout rate of 20%, final sample size needed for each group was estimated to be 30.

Randomization and Allocation Concealment

With a 1:1 allocation and block randomization of block sizes 2 and 4, a randomization sequence was generated using Excel, 2007 by an independent doctor. Allocation details were noted on the cards and sealed in opaque envelopes, which were then numbered, so that the investigator was concealed about the allocation. Generation of random allocation sequence, enrollment, and assignment of participants to intervention were done by an independent doctor who is not involved in the clinical trial.

Blinding

Participants, outcome assessor, and data analyst were blinded to the sample distribution, whereas the operator could not be blinded because of the difference in the physical form of interventions, one is liquid and the other one is powder and liquid.

Interventions and Procedure

After obtaining the written informed consent from the parents, 60 teeth, 30 in each group, were assigned randomly to the test group (propolis) or the control group (MTA). Children allocated to test group (propolis) were subjected to patch test to rule out any allergic tendencies to propolis. After confirming that patient is nonallergic, pulpotomy procedure was carried out under strict aseptic conditions.

In both the groups, anesthesia was given to the teeth and rubber dam was applied for isolation. After removing all the carious debris, a number 4 round bur was used with high-speed handpiece and water spray to get access to the pulp chamber. After that, the pulp chamber was deroofed with a number 330 bur, pulp tissue in the coronal part was scooped out with a sharp spoon excavator, and then saline was flushed to clear off the debris. After achieving hemostasis, respective pulpotomy agent was placed.

In test group, cotton pellet soaked in propolis (Brazilian green propolis alcohol free 60%, Uniflora Health foods, Brazil) was applied on the remaining radicular pulp stumps for 5 minutes, observed for hemostasis, and then restored with glass-ionomer cement (GIC). In control group, MTA (Angelus white, Angelus Industria de Produtos Odontologicos Ltd, Brazil) mixed in 3:1 proportion was placed over the exposed pulp and then restored with GIC. All the treated teeth were given stainless steel crowns and the children were instructed to inform if there is any pain or swelling. For postoperative evaluation, the patients were followed up at 6, 12, and 24 months of interval.

In the recall visits, all the teeth were evaluated to grade them as either success or failure depending on the clinical and radiographic outcomes. The treatment outcome was considered as success when there was no pain, tenderness, sinus opening, and mobility clinically, and no signs of widening of periodontal ligament space, periapical or inter-radicular radiolucency, and internal or external pathological root resorptions radiographically. Any tooth which showed any signs or symptoms of failure was treated with pulpectomy. All the follow-up evaluations were done by a blinded clinician.

Statistical Methods

The collected data was statistically analyzed using nonparametric Chi-square test in IBM SPSS Statistics, version 21 (IBM Corp., Armonk, New York, USA). For all the tests, a ˝p˝ value of 0.05 or less was set for statistical significance.

RESULTS

Participation of subjects through the trial is illustrated in CONSORT flow diagram (Flowchart 1). Out of 60 children, 30 children were randomly assigned to propolis group and 30 to MTA group. All the children received the interventions without any losses or exclusions. Participants were on average 6 years old (range: 4- 8 years). There were almost similar numbers of boys and girls. At the 6-month evaluation period, one boy in the MTA group did not turn up for follow-up, as the family migrated to other state. Hence, the final sample consisted of 59 children.

Flowchart 1: CONSORT flow diagram

Overall success rate of pulpotomy with propolis and MTA at the end of 24 months was found to be 80% (n = 24) and 93.1% (n = 27) respectively and no significant difference was noted between the groups (p = 0.142) (Table 1).

Table 1: Treatment outcome of propolis and MTA at different follow-up intervals
Groups Follow-up intervals
6 months 12 months 24 months
Success Failure Success Failure Success Failure
Propolis 90%(n = 27) 10%(n = 3) 80%(n = 24) 20%(n = 6) 80%(n = 24) 20%(n = 6)
MTA 93.1%(n = 27) 6.9%(n = 2) 93.1%(n = 27) 6.9%(n = 2) 93.1%(n = 27) 6.9%(n = 2)
p = 0.669, NS p = 0.142, NS p = 0.142, NS

Chi-square test; NS: not significant.

At 6 months of follow-up, 59 teeth were evaluated. Three failures were seen in propolis group, whereas MTA group has shown two failures. Propolis and MTA have demonstrated a success rate of 90% (n = 27) and 93.1% (n = 27) respectively and this difference was of no statistical significance (p = 0.669) (Table 1).

At 12 months of interval, the success rate of propolis group reduced to 80% (n = 24) with three more failures, whereas the success rate of MTA remained the same with no more failures and the difference was of no significance (p = 0.142) (Table 1).

Finally at 24 months, no further failures were reported in either of the groups and the success rate remained same as 12 months of interval (Table 1).

Radiographs of cases treated with propolis and MTA are illustrated in Figures 1 and 2 respectively which show no pathological signs at any of the follow-up intervals.

Figs. 1A to D: Radiographs of tooth 74 treated with propolis; (A) Preoperative image; (B) 6-month follow-up image; (C) 12-month follow-up image; (D) 24-month follow-up image

Figs. 2A to D: Radiographs of tooth 74 treated with MTA; (A) Preoperative image; (B) 6-month follow-up image; (C) 12-month follow-up image; (D) 24-month follow-up image

DISCUSSION

Primary teeth with coronally inflamed pulps can be managed with pulpotomy, a vital pulp therapy technique. Pulpotomy in the primary dentition is classified into three categories: devitalization; preservation; and regeneration.8 Among these three lines, preservation and regeneration are the most desirable approaches to preserve the vitality of radicular pulp.

Biocompatible materials with regenerative potential have drawn the momentum in vital pulp therapy. MTA has emerged as most popular material because of its well-accepted biocompatibility, quality biological seal, and tissue regenerative properties. Several studies have tested MTA as pulpotomy medicament in primary molars and reported high success rates when compared to conventional pulpotomy medicaments.6,7,9,10 Hence, in the present study, we preferred MTA as control group.

Propolis is a natural, resinous bee hive extract, and has gained the attention of researchers in recent times because of its antibacterial, anti-inflammatory, antioxidant, and tissue-regenerative properties. Propolis has wide range of applications in medicine and dentistry. In dentistry, it has been tested for root canal irrigation,11 direct and indirect pulp capping,4,12 mouth rinsing,13 and as storage medium for avulsed tooth.14 Owing to the beneficial properties of propolis, it has been considered as test group.

MTA had a high success rate of 93.1% at 24 months of follow-up in the current trial and similar success rates ranging from 94 to 100% at 12- 74 months of follow-up period have been reported by various authors.6,7,9,10 The high success rate of MTA is perhaps as a result of its biocompatibility,15 excellent sealing ability,16,17 alkalinity,15 and its unique ability to induce tissue regeneration when it is placed on the dental pulp.18,19 Although high success rates are reported with MTA, the factors limiting the routine use of MTA are its high cost, technique sensitivity of the material, and difficulty in re-entry into the canal in cases of pulp canal obliteration in teeth indicated for further pulp therapy.

In the present study, propolis demonstrated a success rate of 80% at 24 months of follow-up. The clinical success rates of 84% at 9 months of follow-up and 88.2% at 12 months of follow-up were reported by previous clinical trials.20,21 A higher short-term success rate of 93.3% was reported by Hugar et al. at 6 months of follow-up22 and similar trend has been observed in the present study too.

The success of propolis could be attributed to its antibacterial,2 anti-inflammatory properties3 as well as its biocompatibility,23 ability of dentin bridge formation4,5 and wound healing augmentation.24 Several studies have demonstrated the significant antibacterial efficacy of propolis against E. faecalis , S. mutans, and Lactobacillus .11,25,26 Antimicrobial activity of propolis is due to its components flavonoids, cinnamic acid, caffeic acid, and benzoic acid, which perhaps act on the microbial membrane, inflicting structural, and functional damage.27

It has been reported that propolis inhibits inflammation by regulating cytokines and inflammatory mediators.28 A significant anti-inflammatory effect of Albanian propolis has been demonstrated after 3 months of pulpotomy in piglets.29 Propolis demonstrated superior biocompatibility and cell viability similar to MTA.23 Propolis also enhances wound healing of the underlying radicular tissue at the pulpotomized site. Constituents of propolis increase the production of transforming growth factor-ß, which stimulates the production of collagen by cells.30

Propolis also favors the hard tissue dentin bridge formation when used for direct pulp capping and pulpotomy. Studies have demonstrated the formation of continuous and thicker dentine bridge along with the adjoining well aligned odontoblast-like cell layer.4,5 Meto et al. demonstrated significantly greater regenerative effect and dentin barrier formation with Albanian propolis after 3 months of pulpotomy in piglets.29 An immune-histochemical evaluation of Fibronectin and Tenascin, the markers of dentinogenesis, following direct pulp capping with propolis in dog’s teeth found an increase in the expression of fibronectin and tenascin from 7 to 30 days interval, which suggests the hard tissue barrier formation.31

In the present study, alcohol-free propolis has demonstrated a clinically acceptable success rate as pulpotomy medicament both in short term and long term. Considering its low cost and ready availability, it can be recommended as a pulpotomy medicament for primary teeth. This study gives a further scope to carry out clinical trials with large sample size to authenticate the success of propolis.

CONCLUSION

Propolis has demonstrated a clinically acceptable success rate comparable to MTA as pulpotomy medicament in primary teeth and hence it could be considered as cost-effective option for primary teeth pulpotomy.

REFERENCES

1. Lewis BB Chestner SB. Formaldehyde in dentistry: A review of mutagenic and carcinogenic potential. J Am Dent Assoc 1981;103(03):429-434. DOI: 10.14219/jada.archive.1981.0341

2. Ferreira FB Torres SA Rosa OP et al. Antimicrobial effect of propolis and other substances against selected endodontic pathogens. Oral Surg Oral Med Oral Pathol Oral Radiol Endod 2007;104(05):709-716. DOI: 10.1016/j.tripleo.2007.05.019

3. Tan-No K Nakajima T Shoji T et al. Anti-inflammatory effect of propolis through inhibition of nitric oxide production on carrageenin-induced mouse paw edema. Biol Pharm Bull. 2006;29(01):96-99. DOI: 10.1248/bpb.29.96

4. Parolia A Kundabala M Rao NN et al. A comparative histological analysis of human pulp following direct pulp capping with Propolis, mineral trioxide aggregate and Dycal. Aust Dent J 2010;55(01):59-64. DOI: 10.1111/j.1834-7819.2009.01179.x

5. Ozorio JE Carvalho LF de Oliveira DA et al. Standardised propolis extract and calcium hydroxide as pulpotomy agents in primary pig teeth. J Dent for child (Chic) 2012;79(02):53-58.

6. Farsi N Alamoudi N Balto K et al. Success of mineral trioxide aggregate in pulpotomized primary molars. J Clin Pediatr Dent 2005;29(04):307-311. DOI: 10.17796/jcpd.29.4.n80t77w625118k7

7. Oliveira TM Moretti AB Sakai VT et al. Clinical, radiographic and histologic analysis of the effects of pulp capping materials used in pulpotomies of human primary teeth. Eur Arch Paediatr Dent 2013;14(02):65-71. DOI: 10.1007/s40368-013-0015-x

8. Ranly DM. Pulpotomy therapy in primary teeth: New modalities for old rationales. Pediatr Dent 1994;16(06):403-409.

9. Holan G Eidelman E Fuks AB. Long-term evaluation of pulpotomy in primary molars using mineral trioxide aggregate or formocresol. Pediatr Dent 2005;27(02):129-136.

10. Jabbarifar SE Khademi AA Ghasemi D. Success rate of formocresol pulpotomy versus mineral trioxide aggregate in human primary molar tooth. J Res Med Sci 2004;9(6):304-307.

11. Verma MK Pandey RK Khanna R et al. The antimicrobial effectiveness of 25% Propolis extract in root canal irrigation of primary teeth. J Indian Soc Pedod Prev Dent 2014;32(02):120-124. DOI: 10.4103/0970-4388.130786

12. Sabir A Tabbu CR Agustiono P et al. Histological analysis of rat dental pulp tissue capped with propolis. J Oral Sci 2005;47(03):135-138. DOI: 10.2334/josnusd.47.135

13. Dodwad V Kukreja BJ. Propolis mouthwash: A new beginning. J Indian Soc Periodontol 2011:15(02):121-125. DOI: 10.4103/0972-124X.84379

14. Ozan F Polat ZA Er K et al. Effect of propolis on survival of periodontal ligament cells: new storage media for avulsed teeth. J Endod 2007;33(05):570-573. DOI: 10.1016/j.joen.2006.12.021

15. Torabinejad M Hong CU McDonald F et al. Physical and chemical properties of a new root-end filling material. J Endod 1995a;21(07):349-353. DOI: 10.1016/S0099-2399(06)80967-2

16. Sarkar NK Caicedo R Ritwik P et al. Physicochemical basis of biological properties of mineral trioxide aggregate. J Endod 2005;31(02):97-100. DOI: 10.1097/01.don.0000133155.04468.41

17. Shipper G Grossman ES Botha AJ et al. Marginal adaptation of mineral trioxide aggregate (MTA) compared with amalgam as a root- end filling material: a low vacuum (LV) versus high vacuum (HV) SEM study. Int Endod J 2004;37(05):325-336. DOI: 10.1111/j.0143-2885.2004.00806.x

18. Salako N Joseph B Ritwik P et al. Comparison of bioactive glass, Mineral trioxide aggregate, ferric sulfate and formocresol as pulpotomy agents in rat molar. Dent Traumatol 2003;19(06):314-320. DOI: 10.1046/j.1600-9657.2003.00204.x

19. Agamy HA Bakry NS Mounir MM et al. Comparison of mineral trioxide aggregate and formocresol as pulp capping agents in pulpotomized primary teeth. Pediatr Dent 2004;26(04):302-309.

20. Kusum B Rakesh K Richa K. Clinical and radiographical evaluation of mineral trioxide aggregate, biodentine and propolis as pulpotomy medicaments in primary teeth. Restor Dent Endod 2015;40(04):276-285. DOI: 10.5395/rde.2015.40.4.276

21. Alolofi H EI-Saved M Taha S. Clinical and radiographical evaluation of propolis and thymus vulgaris extracts compared with formocresol pulpotomy in human primary molars. BDJ Open 2016;29;2:16005.

22. Hugar SM Kukreja P Hugar SS et al. Comparative evaluation of Clinical and Radiographic Success of Formocresol, Propolis, Turmeric Gel and Calcium Hydroxide on Pulpotomized Primary molars: A preliminary study. Int J Clin Pediatr Dent 2017;10(01):18-23. DOI: 10.5005/jp-journals-10005-1400

23. Al-Haj Ali SN. In vitro toxicity of propolis in comparison with other primary teeth pulpotomy agents on human fibroblasts. J Investig Clin Dent 2016;7(03):308-313. DOI: 10.1111/jicd.12157

24. Bretz WA Chiego DJ Marcucci MC et al. Preliminary report on the effects of propolis on wound healing in the dental pulp. Z Naturforsch C 1998;53(11-12):1045-1048. DOI: 10.1515/znc-1998-11-1217

25. Elbaz GA Elsayad II. Comparison of the antimicrobial effect of Egyptian propolis vs New Zealand Propolis on Streptococcus mutants and Lactobacilli in Saliva. Oral Health Prev Dent 2012;10(02):155-160

26. Mattigatti S Ratnakar P Moturi S et al. Antimicrobial Effect of Conventional Root Canal Medicaments vs Propolis against Enterococcus faecalis, Staphylococcus aureus and Candida albicans. J Contemp Dent Pract 2012;13(03):305-309. DOI: 10.5005/jp-journals-10024-1142

27. Mirzoeva OK Grishanin RN Calder PC. Antimicrobial action of propolis and some of its components: the effects on growth, membrane potential and motility of bacteria. Microbiol Res 1997;152(03):239-346. DOI: 10.1016/S0944-5013(97)80034-1

28. Gebara ECE Lima LA Mayer MPA. Propolis antimicrobial activity against periodontopathic bacteria. Braz J Microbiol 2002;33(4):365-369. DOI: 10.1590/S1517-83822002000400018

29. Meto A Meto A Bimbari B et al. Anti-Inflammatory and Regenerative Effects of Albanian Propolis in Experimental Vital Amputations. Eur J Prosthodont Restor Dent 2016;24(03):145-151. DOI: 10.1922/EJPRD_1492Meto07

30. Ansorge S Reinhold D Lendeckel U. Propolis and some of its constituents down-regulate DNA synthesis and inflammatory cytokine production but induce TGF-beta1 production of human immune cells. Z Naturforsch 2003;58(7-8):580-589. DOI: 10.1515/znc-2003-7-823

31. Moradi S Saghravanian N Moushekhian S et al. Immuno-histochemical Evaluation of Fibronectin and Tenascin Following Direct Pulp Capping with Mineral Trioxide Aggregate, Platelet-Rich Plasma and Propolis in Dogs Teeth. Iran Endod J 2015;10(03):188-192. DOI: 10.7508/iej.2015.03.009

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