Istanbul Medipol University, School of Dentistry, Department of Orthodontics, Istanbul, Turkey.
J Appl Oral Sci. 2019 Jan 7;27:e20180003. doi: 10.1590/1678-7757-2018-0003.
The aim of this study was to evaluate patients' pain levels during four different debonding procedures. The null hypothesis was that the pain perception of the patients undergoing four different debonding applications was not statistically significant different.
One hundred and twenty orthodontic patients who underwent orthodontic debonding were included in this study. The patients were randomly divided into 4 groups according to technique used in the patients. Debonding groups were as follows: Group 1) Conventional debonding group, Group 2) Medication group (acetaminophen was given 1 hour before debonding), Group 3) Soft bite wax group, and Group 4) Soft acrylic bite wafer group. The patients' levels of anxiety and fear of pain were evaluated before debonding, and Numerical Rating Scale (NRS) was applied to evaluate their pain perception during debonding. Mann-Whitney U and Kruskal-Wallis tests were used to evaluate non-normally distributed data. Categorical data analysis were carried by chi-square and McNemar tests. The significance level was set at p<0.05.
Anxiety scores of the patients were not statistically significant between both genders and debonding groups. In the quadrants in which the patients were perceived, the highest pain level was in the left side of the mandible. The teeth in which the highest pain level was perceived were the lower left and upper right lateral incisors. Although there was no statistically significant difference among the pain scores of the patients in each group, quadrant scores of female patients showed significant differences, being the lowest scores in the soft bite wax group.
Majority of the patients had no fear of pain before debonding. Pain levels of the patients in the conventional debonding group were not significantly different from those of the other groups, except quadrant scores of females in the soft bite wax group. The null hypothesis was accepted.
本研究旨在评估四种不同去带环过程中患者的疼痛程度。零假设是,接受四种不同去带环应用的患者的疼痛感知在统计学上没有显著差异。
本研究纳入了 120 名接受正畸去带环的正畸患者。根据患者所采用的技术,将患者随机分为 4 组。去带环组如下:第 1 组)常规去带环组、第 2 组)药物组(在去带环前 1 小时给予对乙酰氨基酚)、第 3 组)软咬蜡组和第 4 组)软丙烯酸咬垫组。在去带环前评估患者的焦虑和疼痛恐惧程度,并使用数字评分量表(NRS)评估他们在去带环过程中的疼痛感知。使用 Mann-Whitney U 和 Kruskal-Wallis 检验评估非正态分布数据。使用卡方和 McNemar 检验分析分类数据。显著性水平设为 p<0.05。
患者的焦虑评分在性别和去带环组之间没有统计学意义。在患者感知的象限中,下颌左侧的疼痛水平最高。感知疼痛水平最高的牙齿是左下和右上侧切牙。虽然各组患者的疼痛评分无统计学差异,但女性患者的象限评分存在显著差异,软咬蜡组的评分最低。
大多数患者在去带环前没有疼痛恐惧。常规去带环组患者的疼痛水平与其他组无显著差异,除了软咬蜡组女性患者的象限评分。零假设被接受。