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Efficacy of an experimental 3% potassium nitrate mouthwash in providing long-term relief from dentin hypersensitivity: An 8-week randomized controlled study (Study 2)

机译:实验3%硝酸钾漱口水的功效在牙本质蛋白超敏反应中提供长期浮雕:8周随机对照研究(研究2)

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Purpose: To evaluate the efficacy of an experimental mouthwash containing 3% potassium nitrate (KNO3) in the relief of dentin hypersensitivity when used as an adjunct to brushing with fluoride toothpaste compared with the use of the same toothpaste alone. Methods: This was a randomized, two-treatment, examiner-blind, parallel-design single-center, 8-week study in healthy subjects with self-reported and clinically diagnosed dentin hypersensitivity. Subjects were randomized to receive either fluoride toothpaste plus 3.0% KNO3 mouthwash or the same fluoride toothpaste alone, and instructed to use their allocated treatment twice daily for the next 8 weeks. Dentin hypersensitivity was evaluated at baseline and following 4 and 8 weeks of treatment through assessment of responses to evaporative (air) and tactile stimuli [measured by the Schiff sensitivity scale/a visual rating scale (VRS) and tactile threshold, respectively], and using the Dentin Hypersensitivity Experience Questionnaire (DHEQ; a validated quality-of-life instrument for dentin hypersensitivity). Results: A total of 135 subjects were randomized and all completed the study. Both treatment groups demonstrated statistically significant improvements in sensitivity from baseline for each clinical measure of sensitivity (P 0.0001) at Week 4 and Week 8. The toothpaste plus mouthwash group showed greater reductions in sensitivity at both timepoints for all clinical measures; between-treatment differences were only statistically significant for responses to an evaporative (air) stimulus (Schiff sensitivity score and VRS) at Week 4. There was evidence of an improvement in dentin hypersensitivity-associated quality of life as measured by changes from baseline in several DHEQ parameters for both treatment groups, but there were no statistically significant differences between treatments.
机译:目的:评估含有3%硝酸钾(KNO3)的实验漱口水中的功效(KNO3)在用作氟化物牙膏的辅助时用作荧光牙膏的辅助,与单独使用相同的牙膏相比。方法:这是一项随机,双治疗,审查,并行设计单中心,在健康受试者的8周的8周的研究中,具有自我报告和临床诊断的牙本质过敏。受试者被随机接受氟化物牙膏加上3.0%KnO3漱口水或同一氟化物牙膏,并指示在未来8周每天每天两次分配治疗。通过评估蒸发(空气)和触觉速度测量(VRS)和触觉阈值(触觉阈值)和使用的触觉(空气)和触觉刺激的反应进行基线和治疗后4和8周治疗牙本质过敏。牙本质素超敏反应经验问卷(DHEQ;牙本质过敏的验证的寿命质量仪器)。结果:总共135名受试者随机化,全部完成该研究。两种治疗组在第4周和第8周的每种临床敏感性临床措施(P< 0.000)的基线上表现出统计学上显着的改善。牙膏加漱口水组表现出所有临床措施的时间点的敏感性更大的敏感性;治疗差异在第4周对蒸发(空气)刺激(Schiff敏感度和VRS)的反应的统计学意义仅对蒸发(空气)刺激(Schiff敏感度得分和VRS)进行统计学意义。有证据表明牙本质素超敏关系相关的生活质量有所改善,从几个基线中的变化测量两种治疗组的DHEQ参数,但治疗之间没有统计学上显着的差异。

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