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The purpose of this study was to determine the most painful site of infiltration injection in the anterior part of maxilla.
This single-blinded clinical trial was conducted on thirty healthy volunteers. The participants received three maxillary infiltrations injected at the region of central and lateral incisors as well as canines at three separated appointments with a 2-week interval. The outcome variable was pain that measured immediately after needle insertion (time = 0) and during injection of anesthetic solution in 5, 30, and 55 s by a visual analog scale. Data were analyzed by SPSS software version 16 using Friedman test.
There was no statistically significant difference in terms of needle insertion pain and during injection (time = 0, 5, 30, and 55 s) (P = 0.319,P= 0.849,P= 0.627, and P= 0.939, respectively) in the three injection sites.
The pain intensity of infiltration was not associated with injection sites in the anterior maxilla.
Providing an effective, safe, and painless anesthesia is one of the most important skills of a dentist. Anesthetic injection is probably the most significant cause of patients' fear, and an inability to favorably control the pain with minimal discomfort in patients has still remained a noticeable challenge for dentists. Providing a proper anesthesia depends on sufficient knowledge about the anatomy of nervous system, familiarity with the anesthetics, and recognition of existing techniques.
Pain is an unpleasant sensation and an exciting experience accompanied by actual or possible tissue damages.
Injection site has been reported as a factor affecting the pain perceived by the patient.
It is necessary to identify painful injection sites and to make an attempt to minimize the pain on injection clinically. To our knowledge, few studies have been conducted about the effect of injection site on pain intensity.
This single-blinded clinical trial was carried out on thirty volunteered samples. The participants were called over and selected based on the inclusion criteria of a clinical trial. This study was approved by the Regional Bioethics Committee of Kermanshah University of Medical Sciences and has been registered in the Iran Registry for Clinical Trial (IRCT2014091714333n20). All clinical analyses were carried out at the Endodontic Department of Kermanshah School of Dentistry, Kermanshah, Iran, from June to September, 2014. Participants in the study were volunteers and were allowed to quit at any stage of the study. Informed consent was also taken from the participants.
The inclusion criteria of the present study were general health, lack of allergy to lidocaine and epinephrine, no use of any anesthetic, sedatives, and antidepressants over the past 2 weeks, having at least six healthy maxillary anterior teeth without restoration and with proper response to vital tests, not feeling of pain in these six teeth in response to percussion and palpation stimuli, and no history of surgery on the anterior maxilla. The diagnosis of healthy pulp was performed via responses to electrical pulp tester (Parkell, Farmington, USA).
Infiltration was performed on each participant in one of the three regions adjacent to the apex of the maxillary central and lateral incisors and canines over three separated appointments with a 2-week interval. Fifteen participants received injection in the right maxilla and the other 15 participants received injection in the left maxilla. The selection of injection sites, whether right or left region, in each time and classification of participants were carried out randomly (simple method).
A cartridge containing 1.8 mL of 2% lidocaine and 1:80,000 epinephrine (persocaine-E, Daru Pakhsh, Tehran, Iran) was used for anesthetic administration. Needle 27 G (C-K JECT Korea) was used. The injections were performed in the vestibule at the root of maxillary central and lateral incisors and canines under similar conditions (beveled tip of the needle toward the bone, needle penetration depth of 4 mm, and cartridge discharge time of 1 min). The injection speed for all cases was the same (1.8 mL/1 min), and all injections were performed by one person (RSH).
Immediately after needle insertion, the perceived pain level was evaluated in participants through a visual analog scale (VAS) with 0 (no pain) to 10 (maximum pain) calibration by another person (PB) 5, 30, and 55 s during administration of anesthetic solution.
Descriptive and bivariate statistics were computed by SPSS 16 (SPSS Inc., Chicago, IL, USA) using Friedman test with P = 0.05.
This study was performed on thirty healthy volunteers (17 male and 13 female) with the age range of 25–40 years during three stages with 2-week interval. There were no significant differences in pain level immediately after needle insertion between central incisors, lateral incisors, and canines [P = 0.319,
Level of pain during the injection on central incisors, lateral incisors, and canines at the three time periods.
The main aim of this study was to determine the most painful site of maxillary anterior infiltrations. Administration of anesthetics prior to dental treatments is one of the most common procedures during dental treatments, which can basically, due to induction of pain, prevent the patient from visiting the dentist, or cause the incidence of such problems as anxiety during treatment. Several methods have been introduced to reduce the pain due to anesthetic injection, including the use of topical anesthetic gel such as benzocaine,
The findings of the present study showed a similar pain level immediately after injection (0 time) and infiltration in the central and lateral incisors and canines, indicating no significant difference between them. Given the lack of similar studies in this regard, it was not possible to compare the results with other studies. Primosch and Robinson
Pain perception is different in various areas of oral cavity, which depends on the distribution of nerve fibers of pain perception. For instance, oral mucosa and periodontal ligament contain the highest amount of nerve terminals, but the number of these nerve terminals is significantly low in submucosal areas.
The findings also showed that the maximum level of pain was in 5 s of injection, followed by a reduction in 30 and 55 s in central incisors, lateral incisors, and canine areas, which was statistically significant. To explain the reduction trend of pain over time, Kudo
Furthermore, the findings of this study indicated no difference between infiltration of maxillary central and lateral incisors and canines in terms of needle insertion pain and pain level during infiltration. It seems that selection of any of these areas for injection depends on the ability and skill of the dentist and clinical condition of the patient.
One of the limitations of this study was that although the study was conducted with a cross-over design, the anxiety level of the patients, which could affect the pain as a confounding factor, was not evaluated, and their psychological reaction to the anxiety resulting from injection or their compatibility with study conditions might be different during the three stages of the study.
The pain intensity of infiltration was not associated with injection sites in the anterior portion of the maxilla.
This article is based on a thesis submitted to the graduate studies office in fulfillment of requirements for the degree of dentistry at the School of Dentistry, Kermanshah University of Medical Sciences, Iran.
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Conflicts of interest
The authors of this manuscript declare that they have no conflicts of interest, real or perceived, financial or non.financial in this article.