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评价 0.05%洗必泰与 0.05%氟化钠联合应用对抑制牙菌斑形成的效果:一项双盲、交叉、菌斑再生长研究。

Evaluation of chlorhexidine 0.05% with the adjunct of fluoride 0.05% in the inhibition of plaque formation: a double blind, crossover, plaque regrowth study.

机构信息

Department of Biomedical, Surgical and Dental Sciences, Centre for Research in Oral Health, IRCCS Istituto Ortopedico Galeazzi, University of Milan, Milan, Italy.

出版信息

Int J Dent Hyg. 2013 Aug;11(3):186-90. doi: 10.1111/idh.12010. Epub 2012 Nov 26.

DOI:10.1111/idh.12010
PMID:23181710
Abstract

OBJECTIVE

The aim of this study was to evaluate the effect of mouthrinses containing 0.05% chlorhexidine + 0.05% fluoride solution on early dental plaque regrowth.

MATERIALS AND METHODS

Thirty periodontally healthy subjects were included in the study. A crossover 4-day plaque regrowth protocol was adopted. The test product was initially used in 15 patients, while a placebo was administered to the other 15 patients. Then, after a washout period, each patient used the other product. No other oral hygiene manoeuvre was allowed. Full-mouth plaque and bleeding scores (FMPS and FMBS) were evaluated at baseline and after 4 days.

RESULTS

All subjects completed the study. The mean age was 27 ± 8.4 years. Five patients were smokers with a mean daily consumption of 1 ± 2.5 cigarettes. FMPS at baseline was 8.0 ± 4.4 for control group and 7.9 ± 3.8 for test group, without significant difference. After the 4-day plaque regrowth the mean FMPS significantly increased to 31.9 ± 16.5 and 36.3 ± 16.1 for control and test group, respectively (no significant difference between the two groups).

CONCLUSIONS

The test product was safe and well tolerated by subjects. The similar outcomes of the two experimental groups suggest that the two products have an equivalent effect on early dental plaque regrowth. Studies with longer follow-up are needed to clarify whether there is a beneficial long-term effect of daily rinses with the tested solution.

摘要

目的

本研究旨在评估含 0.05%洗必泰+0.05%氟化物溶液的漱口水对早期牙菌斑再生长的影响。

材料和方法

本研究纳入 30 名牙周健康受试者。采用 4 天菌斑再生长交叉试验方案。试验产品最初用于 15 名患者,而其他 15 名患者使用安慰剂。然后,在洗脱期后,每位患者使用另一种产品。不允许进行其他口腔卫生措施。在基线和 4 天后评估全口菌斑和出血评分(FMPS 和 FMBS)。

结果

所有受试者均完成了研究。平均年龄为 27 ± 8.4 岁。5 名患者为吸烟者,平均每日吸烟 1 ± 2.5 支。对照组基线时 FMPS 为 8.0 ± 4.4,试验组为 7.9 ± 3.8,无显著差异。经过 4 天的菌斑再生长,对照组和试验组的平均 FMPS 分别显著增加至 31.9 ± 16.5 和 36.3 ± 16.1(两组间无显著差异)。

结论

试验产品安全,受试者耐受良好。两个实验组的结果相似,表明两种产品对早期牙菌斑再生长的效果相当。需要进行更长时间的随访研究,以明确每天使用测试溶液漱口是否具有有益的长期效果。

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