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盐酸米诺环素龈下软膏治疗中重度成人慢性牙周炎:一项随机、双盲、赋形剂对照、多中心研究。

Subgingival minocycline hydrochloride ointment in moderate to severe chronic adult periodontitis: a randomized, double-blind, vehicle-controlled, multicenter study.

作者信息

van Steenberghe D, Bercy P, Kohl J, De Boever J, Adriaens P, Vanderfaeillie A, Adriaenssen C, Rompen E, De Vree H, McCarthy E F

机构信息

Catholic University Leuven, Belgium.

出版信息

J Periodontol. 1993 Jul;64(7):637-44. doi: 10.1902/jop.1993.64.7.637.

DOI:10.1902/jop.1993.64.7.637
PMID:8396177
Abstract

The safety and efficacy of subgingivally-applied 2% minocycline ointment was evaluated in a randomized, double-blind study of 103 adults with moderate to severe periodontitis. Two groups were compared; one received the test minocycline ointment and the other a vehicle control. Both groups had scaling and root planing at baseline, after which the test or control ointments were applied with an applicator into the periodontal pockets at baseline, and at 2, 4, and 6 weeks. Assessment of clinical response was made by measuring probing depth and probing attachment level and gingival bleeding. These measurements were made at baseline prior to scaling and root planing, and at weeks 4 and 12. Microbiological assessment of the subgingival flora was carried out with DNA probes at baseline, and at weeks 2, 4, 6, and 12 to identify and quantify Porphyromonas gingivalis, Prevotella intermedia, and Actinobacillus actinomycetemcomitans. Subgingival minocycline ointment resulted in statistically significantly greater reduction of P. gingivalis at weeks 2, 4, 6, and 12; P. intermedia at weeks 2, 4, 6, and 12; and A. actinomycetemcomitans at weeks 6 and 12. Probing depth reductions were seen for both groups at weeks 4 and 12; however, this reduction was statistically significantly greater in subjects treated with minocycline ointment. Reduction in gingival index and probing attachment gain were seen in both groups, however, the differences between the groups were not statistically significant.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

在一项针对103名中重度牙周炎成人的随机双盲研究中,评估了龈下应用2%米诺环素软膏的安全性和有效性。比较了两组;一组接受试验性米诺环素软膏,另一组接受赋形剂对照。两组在基线时均进行了龈上洁治和根面平整,之后在基线时以及第2、4和6周,使用涂抹器将试验性或对照软膏涂抹到牙周袋中。通过测量探诊深度、探诊附着水平和牙龈出血来评估临床反应。这些测量在龈上洁治和根面平整前的基线时以及第4周和第12周进行。在基线时以及第2、4、6和12周,使用DNA探针进行龈下菌群的微生物学评估,以鉴定和定量牙龈卟啉单胞菌、中间普氏菌和伴放线放线杆菌。龈下米诺环素软膏在第2、4、6和12周使牙龈卟啉单胞菌的减少在统计学上显著更大;在第2、4、6和12周使中间普氏菌减少;在第6和12周使伴放线放线杆菌减少。两组在第4周和第12周时探诊深度均有降低;然而,米诺环素软膏治疗的受试者中这种降低在统计学上显著更大。两组的牙龈指数均降低且探诊附着增加,然而,两组之间的差异无统计学意义。(摘要截短为250字)

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