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多西环素预防高危患者复发性牙周炎的随机对照试验:抗菌活性及胶原酶抑制作用

Randomized controlled trial of doxycycline in prevention of recurrent periodontitis in high-risk patients: antimicrobial activity and collagenase inhibition.

作者信息

McCulloch C A, Birek P, Overall C, Aitken S, Lee W, Kulkarni G

机构信息

Faculty of Dentistry, University of Toronto, Ontario, Canada.

出版信息

J Clin Periodontol. 1990 Oct;17(9):616-22.

PMID:2174446
Abstract

82 patients with a recent history of periodontal abscesses and/or loss of gingival attachment (GAL) despite active periodontal therapy were enrolled in a double-blind, randomized, placebo-controlled trial. Clinical measurements and subgingival scaling were performed every 2 months. If any site exhibited greater than or equal to 2 mm loss of GAL or a periodontal abscess, patients were administered either 100 mg Doxycycline per day for 3 weeks or placebo. During 12 months of monitoring, 55 patients exhibited recurrent active disease and were then randomly assigned to either the Doxycycline or placebo groups. Clinical measurements of GAL and microbiological culture of subgingival bacteria were made at intervals between 1 week and 7 months after completion of the drug regime. Within 7 months, 15 out of 19 patients on placebo exhibited recurrent disease compared to 13 out of 29 patients on Doxycycline, a relative risk reduction of 43% (p less than 0.05) for Doxycycline compared to placebo. Minimal inhibitory concentrations of Doxycycline for subgingival plaque samples from active sites ranged between 25-100 micrograms/ml, which are several fold higher than reported crevicular fluid concentrations for this drug. However gingival crevicular fluid collagenase was inhibited in vitro at concentrations of 5-10 micrograms/ml Doxycycline. These data indicate that Doxycycline provides significant risk reduction of recurrent periodontitis in patients with active disease.

摘要

82例近期有牙周脓肿病史和/或尽管接受了积极的牙周治疗仍有牙龈附着丧失(GAL)的患者参加了一项双盲、随机、安慰剂对照试验。每2个月进行一次临床测量和龈下刮治。如果任何部位的GAL丧失大于或等于2mm或出现牙周脓肿,则患者每天服用100mg强力霉素,持续3周或服用安慰剂。在12个月的监测期间,55例患者出现复发性活动性疾病,然后被随机分配到强力霉素组或安慰剂组。在完成药物治疗后的1周和7个月之间的间隔时间进行GAL的临床测量和龈下细菌的微生物培养。在7个月内,安慰剂组的19例患者中有15例出现复发性疾病,而强力霉素组的29例患者中有13例出现复发性疾病,与安慰剂相比,强力霉素的相对风险降低了43%(p<0.05)。来自活动部位的龈下菌斑样本对强力霉素的最低抑菌浓度在25-100微克/毫升之间,这比该药物报道的龈沟液浓度高几倍。然而,在体外,5-10微克/毫升的强力霉素浓度可抑制龈沟液中的胶原酶。这些数据表明,强力霉素可显著降低活动性疾病患者复发性牙周炎的风险。

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