School of Dentistry, Paulo Picanço School of Dentistry, Fortaleza, Ceará, Brazil.
State University of Ponta Grossa, Ponta Grossa, Paraná, Brazil.
J Evid Based Dent Pract. 2020 Jun;20(2):101406. doi: 10.1016/j.jebdp.2020.101406. Epub 2020 Feb 4.
To evaluate if the topical application of 10% potassium nitrate applied before in-office bleaching is effective to reduce the risk and intensity of tooth sensitivity (TS), as well as to evaluate if its application can jeopardize color change.
A randomized, split-mouth triple-blind clinical trial was conducted on 43 young patients with incisors A2 or darker. Half of the patient's upper arch received either the application of a 10% potassium nitrate or placebo gel for 10 min in a university setting. In-office bleaching was performed in three 15-min applications in two clinical sessions (1-week interval) using 35% hydrogen peroxide. Risk and intensity of TS was recorded with a 0-4 Numeric Rating Scale and a 0-10 Visual Analogue Scale during bleaching, 1 hour, 24 hours, and 48 hours after bleaching. Color was evaluated before and 1 month after bleaching with shade guides (Vita Classical and Vita Bleachedguide) and a spectrophotometer. The risk of TS (McNemar's test) and intensity of TS (Wilcoxon signed-rank for Numeric Rating Scale and paired t-test for Visual Analogue Scale) were statistically evaluated. Color change was compared using paired t-test. Significant level was set at 5%.
No significant difference was observed in the absolute risks of TS between groups (RR = 1.11; 95% CI 0.97 to 1.27; P = .12), which exceeded 87% for both groups. Similarly, no difference in TS intensities was detected (P > .05). Significant whitening was observed with all color measurement instruments with no difference between groups (P > .05).
The topical application of 10% potassium nitrate, before in-office bleaching, did not reduce the risk and intensity of TS and did not jeopardize color change.
评估在诊室漂白前局部应用 10%硝酸钾是否可以降低牙齿敏感(TS)的风险和强度,以及评估其应用是否会影响颜色变化。
在一所大学环境中,对 43 名 A2 或更暗切牙的年轻患者进行了一项随机、分口、三盲临床试验。患者上颌的一半分别接受 10%硝酸钾或安慰剂凝胶应用 10 分钟。诊室漂白在两次临床就诊中进行了三次 15 分钟的应用(间隔 1 周),使用 35%过氧化氢。在漂白过程中、漂白后 1 小时、24 小时和 48 小时,使用 0-4 数字评分量表和 0-10 视觉模拟量表记录 TS 的风险和强度。使用比色板(Vita Classical 和 Vita Bleachedguide)和分光光度计在漂白前和漂白后 1 个月评估颜色。使用配对 t 检验比较颜色变化。显著性水平设为 5%。
两组间 TS 的绝对风险无显著差异(RR=1.11;95%CI 0.97 至 1.27;P=0.12),两组均超过 87%。同样,TS 强度也无差异(P>0.05)。所有颜色测量仪器均观察到明显的增白效果,两组间无差异(P>0.05)。
在诊室漂白前局部应用 10%硝酸钾不会降低 TS 的风险和强度,也不会影响颜色变化。