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对慢性成人牙周炎患者重复使用龈下米诺环素效果的15个月评估。

A 15-month evaluation of the effects of repeated subgingival minocycline in chronic adult periodontitis.

作者信息

van Steenberghe D, Rosling B, Söder P O, Landry R G, van der Velden U, Timmerman M F, McCarthy E F, Vandenhoven G, Wouters C, Wilson M, Matthews J, Newman H N

机构信息

Catholic University, Leuven, Belgium.

出版信息

J Periodontol. 1999 Jun;70(6):657-67. doi: 10.1902/jop.1999.70.6.657.

Abstract

BACKGROUND

A double-blind, randomized, parallel, comparative study was designed to evaluate the long-term safety and efficacy of subgingivally administered minocycline ointment versus a vehicle control.

METHODS

One hundred four patients (104) with moderate to severe adult periodontitis (34 to 64 years of age; mean 46 years) were enrolled in the study. Following scaling and root planing, patients were randomized to receive either 2% minocycline ointment or a matched vehicle control. Study medication was administered directly into the periodontal pocket with a specially designed, graduated, disposable applicator at baseline; week 2; and at months 1, 3, 6, 9, and 12. Scaling and root planing was repeated at months 6 and 12. Standard clinical variables (including probing depth and attachment level) were evaluated at baseline and at months 1, 3, 6, 9, 12, and 15. Microbiological sampling using DNA probes was done at baseline; at week 2; and at months 1, 3, 6, 9, 12, and 15.

RESULTS

Both treatment groups showed significant and clinically relevant reductions in the numbers of each of the 7 microorganisms measured during the entire 15-month study period. When differences were detected, sites treated with minocycline ointment always produced statistically significantly greater reductions than sites which received the vehicle control. For initial pockets > or =5 mm, a mean reduction in probing depth of 1.9 mm was seen in the test sites, versus 1.2 mm in the control sites. Sites with a baseline probing depth > or =7 mm and bleeding index >2 showed an average of 2.5 mm reduction with minocycline versus 1.5 mm with the vehicle. Gains in attachment (0.9 mm and 1.1 mm) were observed in minocycline-treated sites, with baseline probing depth > or =5 mm and > or =7 mm, respectively, compared with 0.5 mm and 0.7 mm gain at control sites. Subgingival administration of minocycline ointment was well tolerated.

CONCLUSIONS

Overall, the results demonstrate that repeated subgingival administration of minocycline ointment in the treatment of adult periodontitis is safe and leads to significant adjunctive improvement after subgingival instrumentation in both clinical and microbiologic variables over a 15-month period.

摘要

背景

设计了一项双盲、随机、平行、对照研究,以评估龈下应用米诺环素软膏与赋形剂对照的长期安全性和有效性。

方法

104例年龄在34至64岁(平均46岁)的中重度成人牙周炎患者纳入本研究。在进行龈上洁治和根面平整后,患者被随机分为两组,分别接受2%米诺环素软膏或匹配的赋形剂对照。研究药物在基线、第2周、第1、3、6、9和12个月时,通过专门设计的、刻度式一次性给药器直接注入牙周袋。在第6和12个月时重复进行龈上洁治和根面平整。在基线、第1、3、6、9、12和15个月时评估标准临床变量(包括探诊深度和附着水平)。在基线、第2周、第1、3、6、9、12和15个月时,使用DNA探针进行微生物采样。

结果

在整个15个月的研究期间,两个治疗组所检测的7种微生物数量均出现了显著且具有临床意义的减少。当检测到差异时,米诺环素软膏治疗的部位总是比接受赋形剂对照的部位产生统计学上显著更大的减少。对于初始袋深≥5mm的部位,试验组探诊深度平均减少1.9mm,而对照组为1.2mm。基线探诊深度≥7mm且出血指数>2的部位,米诺环素治疗组平均减少2.5mm,而赋形剂对照组为1.5mm。在米诺环素治疗的部位,基线探诊深度≥5mm和≥7mm时,附着增加分别为0.9mm和1.1mm,而对照组分别为0.5mm和0.7mm。龈下应用米诺环素软膏耐受性良好。

结论

总体而言,结果表明,在成人牙周炎治疗中重复龈下应用米诺环素软膏是安全的,并且在15个月的时间里,在临床和微生物学变量方面,龈下器械治疗后能带来显著的辅助改善。

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