Journal of Conservative Dentistry
Home About us Editorial Board Instructions Submission Subscribe Advertise Contact e-Alerts Login 
Users Online: 792
Print this page  Email this page Bookmark this page Small font sizeDefault font sizeIncrease font size

Table of Contents   
Year : 2022  |  Volume : 25  |  Issue : 1  |  Page : 9-19
Analgesic efficacy of corticosteroids and nonsteroidal anti-inflammatory drugs through oral route in the reduction of postendodontic pain: A systematic review

1 Department of Conservative Dentistry and Endodontics, Saveetha Dental College, Saveetha Institute of Medical and Technical Sciences, Chennai, Tamil Nadu, India
2 Department of Conservative Dentistry and Endodontics, Mamata Institute of Dental Sciences, Bachupally, Hyderabad, Telangana State, India

Click here for correspondence address and email

Date of Submission15-Jan-2021
Date of Decision16-Feb-2021
Date of Acceptance19-Feb-2021
Date of Web Publication02-May-2022


Analgesic medications in dentistry are indicated for the relief of acute pain, postoperative pain, chronic pain as well as controlling adjunctive intraoperative pain. The use of nonsteroidal anti-inflammatory drugs (NSAIDs) has shown an effective reduction of postendodontic pain by action on the cyclooxygenase pathway. Another medication which is used recently is corticosteroid which enables the reduction of pain. They are hormones secreted from the adrenal gland and have strong anti-inflammatory actions. This review aims to compare the analgesic efficacy of NSAIDs and corticosteroids when administered through oral route for reducing postendodontic pain. The secondary objective was to assess the anesthetic effect of the nerve block when an oral premedication of NSAIDs or corticosteroids was administered. The databases of PubMed, ScienceDirect, LILACS, and Cochrane were searched for related topics from 1983 to April 2020. Bibliographies of clinical studies were identified in the electronic search. Clinical studies with postendodontic pain reduction using NSAIDs and corticosteroids were selected. Clinical studies that met all inclusion criteria were reviewed. Data extraction was performed independently by two reviewers. All individuals who administered single dose analgesic (NSAID or corticosteroid) before initiating root canal treatment were taken into inclusion criteria. All the relevant data were extracted from the selected studies were reviewed by two independent reviewers using a standardized data collection form, and in case of disagreement, a third reviewer was enquired to achieve a consensus. Risk of bias of the selected studies was done using Cochrane Risk of Bias Tool (version 1). Mean pain score levels at various time intervals showed an increased analgesic success rate for corticosteroids (32-1) in comparison to NSAIDs (32-21.4). Anesthetic effect of the nerve block administered was seen to be better when an oral premedication of corticosteroids (38.2%–80.8%) was given in comparison to NSAID (25.5%–73.1%). From the present study, it can be concluded that oral administration of corticosteroids provides a better analgesic efficacy when compared to NSAIDs as an oral premedication for postoperative pain reduction. It can also be concluded that corticosteroids when used as an oral premedication provide a better anesthetic effect of the nerve block administered when compared to NSAIDs given as an oral premedication. These findings could help the clinician determine which pretreatment analgesic would have a better effect in reduction of pain posttreatment as well as increasing the anesthetic efficacy of administered block. Systematic Review Registration Number: CRD42021235394.

Keywords: Adrenal cortex hormones; analgesics; anti-inflammatory agents; nerve block; pain

How to cite this article:
Jose J, Teja KV, Palanivelu A, Khandelwal A, Siddique R. Analgesic efficacy of corticosteroids and nonsteroidal anti-inflammatory drugs through oral route in the reduction of postendodontic pain: A systematic review. J Conserv Dent 2022;25:9-19

How to cite this URL:
Jose J, Teja KV, Palanivelu A, Khandelwal A, Siddique R. Analgesic efficacy of corticosteroids and nonsteroidal anti-inflammatory drugs through oral route in the reduction of postendodontic pain: A systematic review. J Conserv Dent [serial online] 2022 [cited 2022 Aug 12];25:9-19. Available from:

   Introduction Top

The primary reason people seek endodontic treatment is for the reduction of tooth pain.[1] In endodontic practice, posttreatment pain is a continuous problem faced by dental professionals. Persistent pain associated with teeth after nonsurgical endodontic treatment has been used as an indicator of treatment failure.[2] Patients who exhibit postoperative pain have shown to be about 80%, with pain levels shown to be moderate-to-severe levels.[3] Pain is a subjective experience and is influenced by various factors such as personality, physical, age, and psychological factors. An individual's ability to cope with pain depends on the individual's resistance to infection, which is varied among different individuals. Postendodontic pain occurs in an individual by stimulation of the various pain receptors. The pain signals are conducted via thin fibers containing unmyelinated C-fibers and myelinated A-δ fibers of primary sensory neurons and secondary order neurons in the spinal cord.[4]

Pain is a subjective experience that is shown to experience in different ways in different individuals. It is seen to have multifactorial sources such as microbial causes, host factors, or mechanical factors.[5] All these factors have a direct influence on the intensity of pain the individual experiences. During the treatment procedure, various factors have a confounding effect on the cause of postoperative pain. For instance, Manfredi et al.[6] came to a conclusion that single-visit and multi-visit endodontic therapies have shown a similar level of pain occurrence posttreatment in individuals and are often done by the operator to reduce chairside time. Pulpal status is one of the crucial factors to be considered during endodontic therapy and is innervated by trigeminal afferent axons.[7] Pain is seen to occur in pulp status diagnosed with symptomatic pulpitis and periodontitis and mostly is seen due to infection origin.[8] This is due to different neuropeptides released when different nerve endings are excited in the tooth such as A-fibers and C-fibers.[9] Intracanal irrigants and medicaments commonly are employed to reduce the microbial load in the canal and are used in conjugation with instrumentation process ultimately providing an inert environment for an effect three-dimensional seal.[10] Sodium hypochlorite (NaOCl) is one of the most commonly used intracanal irrigants and has been shown to influence the postoperative pain levels. Farzaneh et al.[11] in their study evaluated different concentrations of NaOCl for reduction of postoperative pain and came to a conclusion that 5.25% NaOCl was much in reduction of pain in comparison to 2.5% NaOCl. Similarly, intracanal medicaments are also shown to influence postoperative pain levels with double antibiotic paste and calcium hydroxide having similar pain reduction levels in individuals undergoing endodontic therapy.[12]

The major cause of pain for endodontic patients is the release of inflammatory mediators that activate sensory nociceptors surrounding the tooth.[13] Various pathways have shown effective pain reduction by its action on the various pathways present. During this process, chemical mediators are seen to be released at the site such as Toll-like receptors and other inflammatory mediators such as interleukin (IL)-8, IL-6, and IL-1.[14] Cell injury is one of the factors which release pain mediators such as potassium, hydron, histamine, bradykinin, serotonin (5HT), adenosine triphosphate, and nitric acid which act at the variety of receptor site causing the release of arachidonic acid from the cell membranes and metabolized by multiple pathways to a variety of prostanoids.

The use of analgesics has long been used in endodontic practice and is given frequently after an endodontic treatment. The use of nonsteroidal anti-inflammatory drugs (NSAIDs) has been used by practitioners for a long period of time to relieve pain of patients. These are a heterogeneous group of drugs with analgesic, antipyretic, and anti-inflammatory properties with less known side effects with many of the drugs considered as over-the-counter drugs. Its primary mechanism of action is competitive inhibition of cyclooxygenase (COX) enzyme which is responsible for the transformation of arachidonic acid metabolites which helps in transformation into prostaglandins (PGs) and thromboxane.

COX pathway is divided into two main categories: COX-1 is found in most organs and tissues, whereas COX-2 is selective and found only in response to certain stimuli. The inhibition of these COX-2 receptors has shown a great deal of effectiveness in reducing pain and giving an anti-inflammatory effect without any undesirable side effects.[15] Though this is the preferred mechanism of action for all the NSAIDs. It varies based on the NSAID administered; for instance, aspirin, sodium salicylate, and ibuprofen are shown to inhibit the PG synthesis by inhibition of the arachnoid acid production having a central effect. Paracetamol (acetaminophen) is shown to have centrally acting properties as well as weak inhibitors of both COX-1 and COX-2.[16] Other NSAIDs such as mefenamic acid, diclofenac sodium, and piroxicam (oxicam derivatives) are shown to possess both analgesic and anti-inflammatory effects by acting on both PGs and COX pathway (COX-1 and COX-2). Indomethacin is shown to have sufficient anti-inflammatory effect but analgesic action acting on both COX-1 and COX-2 sites, but its use should be warranted since it is shown to have various adverse effects.[17] Certain NSAIDs are shown to affect only COX sites; for instance, meloxicam is shown to have lesser inhibitory effect on PGs but more on COX pathway, mainly COX-2 than COX-1.[18] Celecoxib and rofecoxib (coxib derivatives) are shown to be selective COX-2 inhibitors only with the same analgesic, antipyretic, and anti-inflammatory action with decreased incidence of side effects such as gastric ulcerations during long-term administration compared to other NSAIDs.[19]

Corticosteroids, on the other hand, have multiple action sites with its primary mechanism, seen to reduce PG synthesis which is responsible for inflammation and reducing vascular permeability. These are considered lipophilic molecules with the ability to cross the blood–brain barrier and have various disadvantages, such as fluid retention. Dexamethasone is the most commonly used corticosteroid for pain reduction, with others being prednisone, and prednisolone can also be used.[20] One of the major advantages of dexamethasone is less fluid retention than other steroids and has less mineralocorticoid effect. Glucocorticoids are hormones which are seen to be released from adrenal glands and can have a side effect.[21] Dexamethasone, prednisone, and prednisolone reduce pain in individuals by acting on the PG synthesis which is responsible for inflammation and pain pathway to form. Steroid receptors are also seen in peripheral receptors and central receptors and are responsible for pain conduction; these are also inhibited by the corticosteroids and hence reduce pain. There is no literature till date which has described about the direct comparison of reduction of postendodontic pain of NSAIDs and corticosteroids when administered through oral route. Hence, this systematic review aims to compare the analgesic efficacy of NSAIDs and corticosteroids consumed through oral route for postoperative pain reduction.

Structured question

Do NSAIDs bring about a better analgesic effect when compared to corticosteroids in the reduction of postoperative pain when taken through oral route?

   Materials and Methods Top

This review was conducted and reported in accordance with Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines and was registered in PROSPERO database with registration number CRD42021235394. Detailed search strategies were used for the databases for the identification of studies considered.

A research question was formulated based on the PICO principle: Population: Adult population undergoing endodontic therapy, Intervention: NSAIDs, Comparison: Corticosteroids, and Outcome: Postendodontic pain reduction.

The primary outcome assessment to be done was postoperative pain reduction with NSAIDs and corticosteroids using the Visual Analog Scale (VAS) or Numerical Rating Scale (NRS) at different time intervals. The search databases used were PubMed CENTRAL, LILACS, Google Scholar, and ScienceDirect were searched from 1983 to April 2020 using MeSH words, and all fields with the incorporation of Boolean operators “OR” and “AND” were used for database. The complete search methodology is described in [Table 1].
Table 1: Search strategy of all the databases used

Click here to view

In addition to this, additional hand searching was done in the following journals: International Endodontic Journal, Journal of Endodontics, Journal of Conservative Dentistry, and Restorative Dentistry and Endodontics. No limiters were applied for the search. Reference lists of the reviews and the identified studies were also checked for possible additional studies. The following criteria were followed.

Inclusion criteria

  • Randomized clinical trials (RCTs)
  • Patients of age >15 years indicated for endodontic therapy
  • Clinical trials in which NSAIDs and corticosteroids have been used as comparative groups and administered directly through oral route
  • Trials in which root canal treatment was done with diagnosis of symptomatic, asymptomatic irreversible pulpitis, nonvital pulp in single or multirooted teeth
  • Trials in which pain assessment scale was used such as VAS or NRS for pain evaluation in individuals with intervals up to 2 days
  • Preoperative pain scores of 2 and above.

Exclusion criteria

  • Studies in which no placebo group was used
  • Studies in which incomplete data were seen
  • Trials in which individuals exhibited with apical periodontitis or periapical abscess.

Data extraction

Data extracted consisted of the following:

  • Article identification information – authors and publication year
  • Baseline demographic data – age, sex of participants, and preoperative pulpal status
  • Study characteristics – sample size, number of visits, and the number of groups
  • Intervention feature – NSAIDs and corticosteroids
  • Outcome of interest – postoperative pain scale.

   Results Top

[Figure 1] shows the flowchart of the search strategy followed according to the PRISMA guideline. The main finding of this study was to see to reduction of postendodontic pain using NSAIDs and corticosteroids for the reduction of postendodontic pain. Despite the broad time frame search (1985–2020), only recently have the use of corticosteroids been used in endodontics for postendodontic pain reduction. Shahi et al.[22] in 2013 had conducted the first study to clinically administer an oral dose of corticosteroids for the reduction of postendodontic pain. A recent study by Konagala et al.[23] in 2019 was had used orally administered corticosteroid being dexamethasone and deflazacort with piroxicam for the reduction of postendodontic pain. [Table 2] denotes the list of included studies based on the strict inclusion/exclusion criteria. [Table 3] denotes the summary of the eligible RCT studies, and [Table 4] shows the excluded studies with the reason for exclusion. A total of 1719 articles were identified through various databases such as PubMed, LILACS, ScienceDirect, and Google Scholar. The duplicates were excluded, and 58 articles were identified. Out of these 58 articles, they were assessed thoroughly by going through the title and abstract and excluded. A total of 27 articles were selected based on full-text eligibility and were assessed by two independent examiners (J. J and A. P) according to the inclusion and exclusion criteria and were taken into consideration. In case of disagreement, a third reviewer (A. K) was consulted for consensus. From the selected 27 articles, only 5 articles were considered for the qualitative analysis. Each of the articles was assessed independently by two examiners to avoid bias.
Figure 1: Preferred Reporting Items for Systematic Reviews and Meta-Analyses flowchart of the included studies

Click here to view
Table 2: List of studies included based on criteria selected

Click here to view
Table 3: Summary of the eligible RCT studies

Click here to view
Table 4: List of studies excluded based on the criteria

Click here to view

Risk of bias

The risk of bias of all the included studies[22],[23],[24],[25],[26] was assessed these assessed using the Cochrane risk of bias assessment tool.[27] This tool was used since it is shown to have a high sensitivity rate and is shown to give a comprehensive method to assess the potential risk of bias, especially in randomized control trial studies.[28] From the included studies, seven domains were assessed: random sequence generation, allocation concealment, blinding of participants and personnel, blinding of outcome assessment, attrition bias, reporting bias, and any other bias which could affect the results of the study. In the assessment, Jorge-Araujo et al.[24] showed an overall good quality since it satisfied all the assessed domains and overall considered to have a low risk of bias whereas Konagala et al.[23] showed an overall poor quality since it had more than two assessed domains in high bias. Rest most of the studies were classified as unclear bias. The risk of bias summary and graph was generated using Review Manager 5 software (Cochrane, London).

[Figure 2] shows the summary of the risk of bias of the included studies, and [Figure 3] shows the graph for risk of bias assessment. [Table 5] shows the risk of bias based on the major criteria, and [Table 6] shows the risk of bias based on the minor criteria. Randomization of all the participants in the included studies were discussed with significant detail with the evaluation methodology of sample size mentioned. Allocation concealment is a methodology to prevent selection bias among the study groups and was discussed with detail in three of the five included studies.[23],[24],[25] None of the included studies mentioned any methodology error which could affect the results of the study. Blinding is an important feature of RCTs which could minimize bias as well as maximize the validity of the results achieved from the study.[29] In regard to blinding procedure followed, three of the five included studies[24],[25],[26] explained with sufficient detail. The remaining two studies did not provide data if the operators treating patients were blinded on which analgesic was administered to the patients. Dropouts of the participants is a crucial factor to be considered and have a detrimental role on the results achieved from the study. Only three out the five included studies discussed about dropouts of the participants with significant detail.[23],[24],[25]
Figure 2: Risk of bias assessment – Summary

Click here to view
Figure 3: Risk of bias assessment – Graph

Click here to view
Table 5: Risk of bias - Major criteria

Click here to view
Table 6: Risk of bias - Minor criteria

Click here to view

   Discussion Top

Pain management is a fundamental aspect to be considered during the treatment of endodontic pain and is vital for the operator to control this for successful endodontic therapy. The assessment of pain is a critical factor in all these studies with various pain scales present to analyze the degree of pain experienced by the patients for the endodontic procedure, such as the NRS, Verbal Rating Scale, and VAS. Most of these scales are verbally or graphically delivered and have different scale ranges.[30] Jensen[31] showed the use of VAS for assessment of pain. It is most commonly used as a 100-mm line with verbal descriptors ranging from “no pain” to “worst imaginable pain.” Many researchers advocate using VAS and NRS because of its greater sensitivity and are highly reproducible, unaffected by any gender, and are much simpler for the patients to use with its failure rate seen to be 4%–11%.[32] From the included studies, all the studies[22],[23],[24],25],[26] have used the VAS for pain assessment except for Jorge-Araújo et al.,[24] who used NRS for the assessment of pain. Some studies[22],[23],[26] have done a preassessment of pain using the pain assessment scale, and the other studies[24],[25] have only done a postendodontic pain evaluation.

In the present review, two out of five included studies[24],[25] had an overall “low” risk of bias with all domains assessed being under low risk. Bidar et al.[26] and Shahi et al.[22] showed an overall “unclear” bias with allocation concealment, blinding, and outcome data not explained with adequate detail in their study. Kongala et al.[23] showed an overall “high” risk of bias since domains such as random sequence generation, allocation concealment, and blinding of participants and personnel were not mentioned adequately considering them as high risk. Overall, most of the studies showed a low risk, and the results of this study can be followed to an extent.

The use of pretreatment analgesia for postendodontic pain is a well-quantified method with numerous studies, proving that pretreatment analgesia has shown a significant decrease in postendodontic pain preoperatively compared to administration postoperatively.[33] Oral prescription of analgesics is the most commonly used method since it is clinically useful and convenient for the patient and the researcher than other modes of administration, such as intramuscular/intravenous injection.[34] All the included studies have used only oral analgesics at various times, followed by which pain assessment was done. NSAIDs for conditions such as irreversible pulpitis have been shown to reduce inflammatory mediators such as PGE2, which has an overall effect in the reduction of postendodontic pain.[35] The first use of corticosteroids in endodontics is by intracanal administration of corticosteroids for pain reduction.[36] Pochapski et al.[37] had initially used an oral administration of corticosteroids as a pretreatment analgesic which had shown to have a significant reduction of postendodontic pain compared to the placebo group. Followed by this study, various authors had different groups to assess the analgesic efficacy of corticosteroids. All the included studies have followed the protocol of administration of pretreatment analgesia.[22],[23],[24],[25],[26] However, the time interval of the administration of the analgesic varied for different authors who could have an effect on the pain score given by the subjects of the study, with all the subjects in all the studies reporting a better tolerance and pain reduction postendodontic treatment after pretreatment analgesic administration.

All the included studies had done a pulp sensibility testing before the endodontic treatment procedure. The different pulp sensibility testing used are cold tests, heat tests, electric pulp testing, test cavity preparation, and local anesthetic test.[38] The most advocated pulp testing method employed by practitioners is cold testing which is ideally done in conjugation with electric pulp testing for accurate results and used to differentiate between reversible and irreversible pulpitis. This is due to the stimulation of the Aδ nerve fibers within the pulp dentinal complex.[39] It is an inexpensive test and used by many clinicians in conjugation with electrical pulp testing. In the present study, most of the authors[22],[24],[25],[26] have used cold test to assess the pulpal status of the tooth with some studies using electrical pulp testing for the confirmation of the assessment.[24],[25] Konagala et al.[23] though had made a pulpal diagnosis for the assessment of pulpal status; the method of assessment has not been mentioned since the thermal tests used are seen to give different response perceptions for the patients.[40] Although their study had combined clinical examination, radiographic findings, and dental history, no mentioning of the thermal test used could have an influence on the selection of the samples and was considered as a bias in our evaluation.

The use of NSAIDs has long been advocated for management of endodontic pain. There are some instances in which the patients have reported side effects such as GI disorders and cardiovascular problems on long-term usage.[41] This, however, did not inhibit the use of NSAIDs for these patients since the side effects exhibited are quite negligible. The use of corticosteroids has shown a high anti-inflammatory action by reduction of the release of arachidonic acid by inhibiting the action of phospholipase-A2.[42] Isett et al.[43] had proven that reducing inflammatory mediators such as PGE2 and IL-8 seen only in cases of irreversible pulpitis had reduced after the administration of corticosteroids. Although it has high inflammatory action, the side effects of the use of corticosteroids are common. Some of them being gastrointestinal bleeding, insomnia, and proximal muscle weakness[44] should not be used continuously for long periods. Even with all these side effects, the usage of corticosteroids as an analgesic has not been hindered since its usage is not limited to a single-frequency consumption. Instead, multiple frequencies of consumption by the same individual show increased side effects. One of the significant factors to be taken notice of is the increased chances of gastric ulcers, as reported by Piper et al.[45] by the drug interaction between corticosteroids and NSAIDs. In spite of this, none of the included studies had patients reported with a problem even after administration of rescue medication.

Two of the included studies by Shahi et al.[22] and Bidar et al.[26] though used NSAIDs and corticosteroids as a premedication, the primary outcome of both the studies was to evaluate the anesthetic efficacy of the inferior alveolar nerve block nevertheless these articles were considered since it followed all the inclusion/exclusion parameters.

The administration of an oral premedication of an analgesic has a direct effect on the anesthetic effect of the nerve block administrated as reported by the included studies in this review. The two included studies[22],[26] followed all the inclusion criteria of the present study though the primary outcome of these studies was to assess the success of the administered nerve anesthetic block. It has been reported that the success rate of nerve blocks decreases by several factors such as anxiety and is drastically decreased in the case of irreversible pulpitis.[46] This is due to the nociceptors by inflammatory mediators such as PGs, which decrease the anesthetic effect of the administered drug.[47] From the included studies, corticosteroids have shown to have a better success rate when administered as an oral premedication than NSAIDs showing a 30% increased success rate when compared to an oral premedication of NSAIDs. The anesthetic efficacy of the nerve block administered was significantly improved when an oral premedication of corticosteroids was given in comparison to NSAIDs.

   Conclusions Top

Most of the studies in the present review showed an overall “low” and “unclear” risk; it can be concluded that oral consumption of corticosteroids has a better analgesic effect when compared to NSAIDs. Although the onset of action of NSAIDs is much better than when compared to corticosteroids, the analgesic effect produced by corticosteroids has a sustained effect for an extended period producing a better analgesic effect. Oral premedication of corticosteroids has a better anesthetic efficacy when compared to NSAIDs. One of the limitations for this review is the number of studies included. The inclusion of studies satisfying the inclusion criteria was limited. It is necessary to do more drug efficacy clinical studies, which can show much better results on the analgesic efficacy of NSAIDs and corticosteroids in postendodontic pain reduction.

Financial support and sponsorship


Conflicts of interest

There are no conflicts of interest.

   References Top

O'Keefe EM. Pain in endodontic therapy: Preliminary study. J Endod 1976;2:315-9.  Back to cited text no. 1
Nixdorf DR, Moana-Filho EJ, Law AS, McGuire LA, Hodges JS, John MT. Frequency of persistent tooth pain following root canal therapy: A systematic review and meta-analysis. J Endod 2010;36:224-30.  Back to cited text no. 2
Marshall JG. Consideration of steroids for endodontic pain. Endod Top 2002;3:41-51.  Back to cited text no. 3
Sacerdote P, Levrini L. Peripheral mechanisms of dental pain: The role of substance P. Mediators Inflamm 2012;2012:951920.  Back to cited text no. 4
Jayakodi H, Kailasam S, Kumaravadivel K, Thangavelu B, Mathew S. Clinical and pharmacological management of endodontic flare-up. J Pharm Bioallied Sci 2012;4:S294-8.  Back to cited text no. 5
Manfredi M, Figini L, Gagliani M, Lodi G. Single versus multiple visits for endodontic treatment of permanent teeth. Cochrane Database Syst Rev 2016;12:CD005296.  Back to cited text no. 6
Byers MR, Närhi MV. Dental injury models: Experimental tools for understanding neuroinflammatory interactions and polymodal nociceptor functions. Crit Rev Oral Biol Med 1999;10:4-39.  Back to cited text no. 7
Estrela C, Guedes OA, Silva JA, Leles CR, Estrela CR, Pécora JD. Diagnostic and clinical factors associated with pulpal and periapical pain. Braz Dent J 2011;22:306-11.  Back to cited text no. 8
Jain N, Gupta A. An insight into neurophysiology of pulpal pain: Facts and hypotheses. The Korean journal of pain 2013;26:347.  Back to cited text no. 9
Glickman GN, Koch KA. 21st-Century endodontics. J Am Dent Assoc 2000;131 Suppl: 39S-46S.  Back to cited text no. 10
Farzaneh S, Parirokh M, Nakhaee N, Abbott PV. Effect of two different concentrations of sodium hypochlorite on postoperative pain following single-visit root canal treatment: A triple-blind randomized clinical trial. Int Endod J 2018;51 Suppl 1:e2-11.  Back to cited text no. 11
Samir Abouelenien S, Mohamed Ibrahim S, Gameel Shaker O, Mohamed Ahmed G. Evaluation of postoperative pain in infected root canals after using double antibiotic paste versus calcium hydroxide as intra-canal medication: A randomized controlled trial. F1000Res 2018;7:1768.  Back to cited text no. 12
Nguyen V, Chen YW, Johnson JD, Paranjpe A. In vivo evaluation of effect of preoperative ibuprofen on proinflammatory mediators in irreversible pulpitis cases. J Endod 2020;46:1210-6.  Back to cited text no. 13
Rechenberg DK, Galicia JC, Peters OA. Biological markers for pulpal inflammation: A systematic review. PLoS One 2016;11:e0167289.  Back to cited text no. 14
Poveda Roda R, Bagán JV, Jiménez Soriano Y, Gallud Romero L. Use of nonsteroidal antiinflammatory drugs in dental practice. A review. Med Oral Patol Oral Cir Bucal 2007;12:E10-8.  Back to cited text no. 15
Hargreaves K, Abbott PV. Drugs for pain management in dentistry. Aust Dent J 2005;50:S14-22.  Back to cited text no. 16
Parirokh M, Ashouri R, Rekabi AR, Nakhaee N, Pardakhti A, Askarifard S, et al. The effect of premedication with ibuprofen and indomethacin on the success of inferior alveolar nerve block for teeth with irreversible pulpitis. J Endod 2010;36:1450-4.  Back to cited text no. 17
Nekoofar MH, Sadeghipanah M, Dehpour AR. Evaluation of meloxicam (A cox-2 inhibitor) for management of postoperative endodontic pain: A double-blind placebo-controlled study. J Endod 2003;29:634-7.  Back to cited text no. 18
Jeske AH. COX-2 inhibitors and dental pain control. J Gt Houst Dent Soc 1999;71:39-40.  Back to cited text no. 19
Vyvey M. Steroids as pain relief adjuvants. Can Fam Physician 2010;56:1295-7.  Back to cited text no. 20
Iranmanesh F, Parirokh M, Haghdoost AA, Abbott PV. Effect of corticosteroids on pain relief following root canal treatment: A systematic review. Iran Endod J 2017;12:123-30.  Back to cited text no. 21
Shahi S, Mokhtari H, Rahimi S, Yavari HR, Narimani S, Abdolrahimi M, et al. Effect of premedication with ibuprofen and dexamethasone on success rate of inferior alveolar nerve block for teeth with asymptomatic irreversible pulpitis: A randomized clinical trial. J Endod 2013;39:160-2.  Back to cited text no. 22
Konagala RK, Mandava J, Pabbati RK, Anupreeta A, Borugadda R, Ravi R. Effect of pretreatment medication on postendodontic pain: A double-blind, placebo-controlled study. J Conserv Dent 2019;22:54-8.  Back to cited text no. 23
Jorge-Araújo AC, Bortoluzzi MC, Baratto-Filho F, Santos FA, Pochapski MT. Effect of premedication with anti-inflammatory drugs on post-endodontic pain: A randomized clinical trial. Braz Dent J 2018;29:254-60.  Back to cited text no. 24
Praveen R, Thakur S, Kirthiga M. Comparative evaluation of premedication with ketorolac and prednisolone on postendodontic pain: A double-blind randomized controlled trial. J Endod 2017;43:667-73.  Back to cited text no. 25
Bidar M, Mortazavi S, Forghani M, Akhlaghi S. Comparison of effect of oral premedication with ibuprofen or dexamethasone on anesthetic efficacy of inferior alveolar nerve block in patients with irreversible pulpitis: A prospective, randomized, controlled, double-blind study. Bull Tokyo Dent Coll 2017;58:231-6.  Back to cited text no. 26
Higgins JP, Altman DG, Gøtzsche PC, Jüni P, Moher D, Oxman AD, et al. The Cochrane Collaboration's tool for assessing risk of bias in randomised trials. BMJ 2011;343:d5928.  Back to cited text no. 27
Jørgensen L, Paludan-Müller AS, Laursen DR, Savović J, Boutron I, Sterne JA, et al. Evaluation of the Cochrane tool for assessing risk of bias in randomized clinical trials: Overview of published comments and analysis of user practice in Cochrane and non-Cochrane reviews. Syst Rev 2016;5:80.  Back to cited text no. 28
Karanicolas PJ, Farrokhyar F, Bhandari M. Blinding: Who, what, when, why, how? Can J Surg 2010;53:345-8.  Back to cited text no. 29
Williamson A, Hoggart B. Pain: A review of three commonly used pain rating scales: Pain rating scales. J Clin Nurs 2005;14:798-804.  Back to cited text no. 30
Jensen M. Interpretation of visual analog scale ratings and change scores: A reanalysis of two clinical trials of postoperative pain. J Pain 2003;4:407-14.  Back to cited text no. 31
Kremer E, Atkinson HJ, Ignelzi RJ. Measurement of pain: Patient preference does not confound pain measurement. Pain 1981;10:241-8.  Back to cited text no. 32
Attar S, Bowles WR, Baisden MK, Hodges JS, McClanahan SB. Evaluation of pretreatment analgesia and endodontic treatment for postoperative endodontic pain. J Endod 2008;34:652-5.  Back to cited text no. 33
Barnhill BJ, Holbert MD, Jackson NM, Erickson RS. Using pressure to decrease the pain of intramuscular injections. J Pain Symptom Manage 1996;12:52-8.  Back to cited text no. 34
Rood JP, Pateromichelakis S. Inflammation and peripheral nerve sensitisation. Br J Oral Surg 1981;19:67-72.  Back to cited text no. 35
Moskow A, Morse DR, Krasner P, Furst ML. Intracanal use of a corticosteroid solution as an endodontic anodyne. Oral Surg Oral Med Oral Pathol 1984;58:600-4.  Back to cited text no. 36
Pochapski MT, Santos FA, de Andrade ED, Sydney GB. Effect of pretreatment dexamethasone on postendodontic pain. Oral Surg Oral Med Oral Pathol Oral Radiol Endod 2009;108:790-5.  Back to cited text no. 37
Alghaithy RA, Qualtrough AJ. Pulp sensibility and vitality tests for diagnosing pulpal health in permanent teeth: A critical review. Int Endod J 2017;50:135-42.  Back to cited text no. 38
Gopikrishna V, Pradeep G, Venkateshbabu N. Assessment of pulp vitality: A review. Int J Paediatr Dent 2009;19:3-15.  Back to cited text no. 39
Salgar AR, Singh SH, Podar RS, Kulkarni GP, Babel SN. Determining predictability and accuracy of thermal and electrical dental pulp tests: An in vivo study. J Conserv Dent 2017;20:46-9.  Back to cited text no. 40
[PUBMED]  [Full text]  
Ho KY, Gwee KA, Cheng YK, Yoon KH, Hee HT, Omar AR. Nonsteroidal anti-inflammatory drugs in chronic pain: Implications of new data for clinical practice. J Pain Res 2018;11:1937-48.  Back to cited text no. 41
Liesinger A, Marshall FJ, Marshall JG. Effect of variable doses of dexamethasone on posttreatment endodontic pain. J Endod 1993;19:35-9.  Back to cited text no. 42
Isett J, Reader A, Gallatin E, Beck M, Padgett D. Effect of an intraosseous injection of depo-medrol on pulpal concentrations of PGE2 and IL-8 in untreated irreversible pulpitis. J Endod 2003;29:268-71.  Back to cited text no. 43
Alexander RE, Throndson RR. A review of perioperative corticosteroid use in dentoalveolar surgery. Oral Surg Oral Med Oral Pathol Oral Radiol Endod 2000;90:406-15.  Back to cited text no. 44
Piper JM, Ray WA, Daugherty JR, Griffin MR. Corticosteroid use and peptic ulcer disease: Role of nonsteroidal anti-inflammatory drugs. Ann Intern Med 1991;114:735-40.  Back to cited text no. 45
Potočnik I, Bajrović F. Failure of inferior alveolar nerve block in endodontics. Dent Traumatol 1999;15:247-51.  Back to cited text no. 46
Ferreira SH. Peripheral analgesic sites of action of anti-inflammatory drugs. International journal of clinical practice. Supplement. 2002;(128):2-10.  Back to cited text no. 47

Correspondence Address:
Dr. Jerry Jose
Department of Conservative Dentistry and Endodontics, Saveetha Dental College, Saveetha Institute of Medical and Technical Sciences, Saveetha University, Chennai - 600 077, Tamil Nadu
Login to access the Email id

Source of Support: None, Conflict of Interest: None

DOI: 10.4103/jcd.jcd_30_21

Rights and Permissions


  [Figure 1], [Figure 2], [Figure 3]

  [Table 1], [Table 2], [Table 3], [Table 4], [Table 5], [Table 6]


    Similar in PUBMED
   Search Pubmed for
   Search in Google Scholar for
 Related articles
    Email Alert *
    Add to My List *
* Registration required (free)  

    Materials and Me...
    Article Figures
    Article Tables

 Article Access Statistics
    PDF Downloaded30    
    Comments [Add]    

Recommend this journal