Mehrvarzfar Payman, Esnashari Ehsan, Salmanzadeh Reyhaneh, Fazlyab Mahta, Fazlyab Mahyar
Department of Endodontics, Dental Branch, Islamic Azad University of Medical Sciences, Tehran, Iran.
Dentist, Tehran, Iran.
Iran Endod J. 2016 Fall;11(4):261-266. doi: 10.22037/iej.2016.2.
The aim of this randomized-controlled clinical trial was to assess the effect of intraligamentary (PDL) injection of dexamethasone on onset and severity of post-treatment pain in patients with symptomatic irreversible pulpitis.
A total number of 60 volunteers were included according to the inclusion criteria and were assigned to three groups (=20). After administration of local anesthesia and before treatment, group 1 (control) PDL injection was done with syringe containing empty cartridge, while in groups 2 and 3 the PDL injection was done with 0.2 mL of 2% lidocaine or dexamethasone (8 mg/2 mL), respectively. Immediately after endodontic treatment patients were requested to mark their level of pain on a visual analogue scale (VAS) during the next 48 h (on 6, 12, 24 and 48-h intervals). They were also asked to mention whether analgesics were taken and its dosage. Considering the 0-170 markings on the VAS ruler, the level of pain was scored as follows: (mild pain; 0-56), (moderate pain; 57-113) and (severe pain; 114-170). The data were analyzed using the Kruskal-Wallis and the Chi-square tests and the level of significance was set at 0.05.
After 6 and 12 h, group 1 and group 3 had the highest and lowest pain values, respectively (<0.01 and <0.001 for 6 and 12 h, respectively). However, after 24 and 48 h the difference in the pain was not significant between groups 1 and 2 (<0.6) but group 3 had lower pain levels (<0.01 and <0.8 for 24 and 48 h, respectively).
Pretreatment PDL injection of dexamethasone can significantly reduce the post-treatment endodontic pain in patients with symptomatic irreversible pulpitis.
本随机对照临床试验的目的是评估在有症状的不可复性牙髓炎患者中,韧带内(牙周膜)注射地塞米松对治疗后疼痛的发作及严重程度的影响。
根据纳入标准共纳入60名志愿者,并将其分为三组(每组 = 20人)。在局部麻醉给药后且治疗前,第1组(对照组)使用装有空针筒的注射器进行牙周膜注射,而第2组和第3组分别使用0.2 mL 2%利多卡因或地塞米松(8 mg/2 mL)进行牙周膜注射。根管治疗结束后,立即要求患者在接下来的48小时内(每隔6、12、24和48小时)在视觉模拟量表(VAS)上标记其疼痛程度。还要求他们提及是否服用了镇痛药及其剂量。考虑到VAS标尺上的0 - 170个标记,疼痛程度评分如下: (轻度疼痛;0 - 56), (中度疼痛;57 - 113)和 (重度疼痛;114 - 170)。使用Kruskal - Wallis检验和卡方检验对数据进行分析,显著性水平设定为0.05。
6小时和12小时后,第1组和第3组分别具有最高和最低疼痛值(6小时和12小时时分别为<0.01和<0.001)。然而,24小时和48小时后,第1组和第2组之间的疼痛差异不显著(<0.6)但第3组的疼痛水平较低(24小时和48小时时分别为<0.01和<0.8)。
治疗前牙周膜注射地塞米松可显著减轻有症状的不可复性牙髓炎患者治疗后的根管治疗疼痛。