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家用药物治疗牙本质过敏症:不同测量方法的临床疗效评估

Home-use agents in the treatment of dentin hypersensitivity: clinical effectiveness evaluation with different measurement methods.

作者信息

Ayan Gizem, Mіsіllі Tuğba, Buldur Mehmet

机构信息

Faculty of Dentistry, Department of Restorative Dentistry, Çanakkale Onsekiz Mart University, Çanakkale, 17100, Turkey.

出版信息

Clin Oral Investig. 2025 Jan 15;29(1):63. doi: 10.1007/s00784-025-06155-1.

Abstract

OBJECTIVES

This study aimed to evaluate the effectiveness of home-use desensitizing agents over an 8-week period by comparing them using different measurement methods.

METHODS

A randomized, controlled clinical trial was conducted with 180 individuals aged between 18 and 70 who clinically diagnosed dentin hypersensitivity (DH) in two or more non-adjacent teeth. Subjects who met the inclusion criteria (n = 164) were randomly allocated into five test groups-using Casein phosphopeptide-amorphous calcium phosphate (CPP-ACP), Arginine, Novamin, Propolis, and Potassium nitrate-and a control group using standard fluoride toothpaste. The status of DH was assessed at week 4 and week 8 by the same independent examiner. Changes from baseline in Dentine Hypersensitivity Experience Questionnaire-15 (DHEQ-15), Schiff Sensitivity Scale (SSS) and Visual Analog Scale (VAS) were analysed using ANOVA and Kruskall-Wallis tests.

RESULTS

All test groups showed statistically significant improvements in DH at weeks 4 and 8 compared to baseline in the DHEQ-15, VAS, and SSS assessments (p < 0.005). In the control group, significant improvements were observed only in the VAS and SSS measurements from baseline to weeks 8 (p < 0.005). The CPP-ACP group demonstrated the greatest reduction in scores by the end of week 8 compared to baseline, with DHEQ-15 (56.68 ± 17.87), VAS (6.52 ± 1.48), and SSS (2.32 ± 0.56).

CONCLUSIONS

Among the tested agents, the CPP-ACP group demonstrated the most notable reduction in DH symptoms by week 8, highlighting its potential as an effective method for alleviating DH symptoms in a home-use agents.

CLINICAL RELEVANCE

Home-use desensitizing agents are effective in the treatment of DH, improving the daily activities of patients who cannot access clinical care and ensuring the relief of DH before clinical invasive procedures.

TRIAL REGISTRATION

ClinicalTrials.gov Identifier: NCT06216262.

摘要

目的

本研究旨在通过使用不同测量方法进行比较,评估家用脱敏剂在8周内的有效性。

方法

对180名年龄在18至70岁之间、临床上诊断为两颗或更多非相邻牙齿牙本质过敏(DH)的个体进行了一项随机对照临床试验。符合纳入标准的受试者(n = 164)被随机分为五个试验组,分别使用酪蛋白磷酸肽 - 无定形磷酸钙(CPP - ACP)、精氨酸、诺瓦敏、蜂胶和硝酸钾,以及一个使用标准含氟牙膏的对照组。由同一位独立检查者在第4周和第8周评估DH的状况。使用方差分析和克鲁斯卡尔 - 沃利斯检验分析牙本质过敏体验问卷 - 15(DHEQ - 15)、希夫敏感量表(SSS)和视觉模拟量表(VAS)相对于基线的变化。

结果

与基线相比,在DHEQ - 15、VAS和SSS评估中,所有试验组在第4周和第8周的DH均有统计学显著改善(p < 0.005)。在对照组中,仅在从基线到第8周的VAS和SSS测量中观察到显著改善(p < 0.005)。与基线相比,到第8周结束时,CPP - ACP组的得分下降幅度最大,DHEQ - 15为(56.68 ± 17.87),VAS为(6.52 ± 1.48),SSS为(2.32 ± 0.56)。

结论

在测试的药剂中,CPP - ACP组在第8周时DH症状减轻最为显著,突出了其作为家用药剂缓解DH症状的有效方法的潜力。

临床意义

家用脱敏剂在治疗DH方面有效,可改善无法获得临床护理的患者的日常活动,并确保在临床侵入性操作前缓解DH。

试验注册

ClinicalTrials.gov标识符:NCT06216262。

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