Kunihira D M, Caine F A, Palcanis K G, Best A M, Ranney R R
J Periodontol. 1985 Jun;56(6):352-8. doi: 10.1902/jop.1985.56.6.352.
A double-blind clinical trial of oral penicillin as an adjunct to conventional treatment of localized juvenile periodontitis (JP) was conducted. Sixteen subjects with JP were paired on the basis of general similarity of disease, and within each pair the persons were assigned randomly, one to a placebo group and one to a penicillin group. Neither patients nor therapist/examiner were aware of whether placebo or penicillin was being taken. All subjects received an initial scaling and root planing of all teeth and flap surgery of all affected sites. Every 12 weeks after surgery through Week 62 of the study, root planing and oral hygiene instructions were repeated. Phenoxymethyl penicillin (250 mg qid) or placebo was started the day of surgery and each recall visit and lasted for 10 days. Clinical measurements were made at the beginning of the study and at each recall visit. In both groups there was a significant decrease in plaque scores, gingival inflammation, gingival bleeding and probeable depths for all sites and for affected sites. Similarly there was a significant increase in attachment level and radiographic bone height, and a total elimination of suppuration. The favorable changes were apparent at the first postsurgical recall (Week 26 of the study) and remained essentially the same through Week 62. The magnitude of change in these parameters was similar to that reported by others for treatment regimes including tetracycline therapy. However, there were no differences in any parameters between the placebo and penicillin groups. Half of the subjects (4 in each group) were continued in the study for another 9 months (Week 98).(ABSTRACT TRUNCATED AT 250 WORDS)
开展了一项双盲临床试验,研究口服青霉素作为局限性青少年牙周炎(JP)常规治疗辅助手段的效果。16名JP患者根据疾病的总体相似性进行配对,在每一对中,两人被随机分配,一人进入安慰剂组,一人进入青霉素组。患者和治疗师/检查者均不知道服用的是安慰剂还是青霉素。所有受试者均接受了全口牙齿的初始洁治和根面平整以及所有患部的翻瓣手术。在手术后至研究第62周期间,每12周重复进行根面平整和口腔卫生指导。苯氧甲基青霉素(250毫克,每日四次)或安慰剂在手术当天及每次复诊时开始服用,持续10天。在研究开始时和每次复诊时进行临床测量。两组中,所有部位和患部的菌斑评分、牙龈炎症、牙龈出血和可探及深度均显著降低。同样,附着水平和影像学骨高度显著增加,化脓现象完全消除。这些有利变化在术后首次复诊时(研究第26周)就很明显,并在第62周基本保持不变。这些参数的变化幅度与其他包括四环素治疗在内的治疗方案所报告的相似。然而,安慰剂组和青霉素组在任何参数上均无差异。一半的受试者(每组4人)继续参与研究另外9个月(第98周)。(摘要截选至250字)