Subantimicrobial dose doxycycline as an adjunct to scaling and root planing: post-treatment effects

被引:64
作者
Caton, JG
Ciancio, SG
Blieden, TM
Bradshaw, M
Crout, RJ
Hefti, AF
Massaro, JM
Polson, AM
Thomas, J
Walker, C
机构
[1] Univ Rochester, Eastman Dent Ctr, Rochester, NY 14620 USA
[2] SUNY Buffalo, Dept Periodont, Buffalo, NY 14260 USA
[3] Icon Clin Res, Norristown, PA USA
[4] W Virginia Univ, Med Ctr, Off Dent Res, Morgantown, WV 26506 USA
[5] Ohio State Univ, Coll Dent, Columbus, OH 43210 USA
[6] Boston Univ, Sch Publ Hlth, Boston, MA USA
[7] Univ Penn, Dept Periodont, Philadelphia, PA 19104 USA
[8] W Virginia Univ, Dept Pathol, Morgantown, WV USA
[9] Univ Florida, Periodontal Dis Res Ctr, Gainesville, FL USA
关键词
doxycycline; subantimicrobial; matrix metalloproteinases; periodontitis; scaling and root planing; post-treatment;
D O I
10.1034/j.1600-051X.2001.280810.x
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
Background/objective: Subantimicrobial dose doxycycline (SDD 20 mg bid) plus scaling and root planing (SRP) significantly improved clinical attachment level (CAL) and reduced probing depth (PD) compared with placebo plus SRP in a double-blind, placebo-controlled, multicenter study of patients with adult periodontitis (AP). In a study conducted as a follow-up, the post-treatment effects of SDD were assessed in patients who completed the SRP study. Methods: The SRP study was a 9-month, active-treatment study and the followup was a 3-month, no-treatment study. In the SRP study, tooth sites in qualifying quadrants were scaled and root planed and patients were randomized to receive twice daily SDD 20 mg or placebo. In the follow-up, patients received no study drug; investigators and patients remained blinded to the previous treatment group assignments. Efficacy measures included the change in CAL and PD from baseline values determined at the start of the SRP study in tooth sites stratified by baseline PD (i.e., 0-3 mm, 4-6 mm, greater than or equal to7 mm). Safety was evaluated using adverse event data and the results of clinical laboratory tests, oral pathology examinations, and microbiological assessments. Results: Within each disease stratum, the incremental improvements in PD and CAL demonstrated in the SDD group over 9 months of active treatment were maintained through 3 additional months of no treatment. Treatment cessation did not result in an accelerated regression of periodontal health. No differences in the incidence of adverse events (including those related to infection) or laboratory or microbiological parameters were noted between the SDD group and the placebo group. Conclusions: The administration of SDD 20 mg bid for a period of up to 9 months is not associated with rebound effects or delayed or negative aftereffects for a 3-month period after cessation of therapy.
引用
收藏
页码:782 / 789
页数:8
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