Department of Periodontology, Dental Research Division, Guarulhos University, Guarulhos, São Paulo, Brazil.
J Clin Periodontol. 2017 Aug;44(8):822-832. doi: 10.1111/jcpe.12721. Epub 2017 Jul 26.
To evaluate the clinical effects of different dosages of metronidazole (MTZ) and durations of MTZ + amoxicillin (AMX) in the treatment of generalized chronic periodontitis (GChP).
Subjects with severe GChP were randomly assigned to receive scaling and root planing (SRP)-only, or combined with 250 or 400 mg of MTZ + AMX (500 mg) thrice a day (TID), for 7 or 14 days. Subjects were monitored for 1 year.
One hundred and nine subjects were enrolled. At 1 year, 61.9% and 63.6% of the subjects receiving AMX + 250 or 400 mg of MTZ for 14 days, respectively, reached the clinical endpoint for treatment (≤4 sites with probing depth ≥5 mm), against 31.8% of those taking 250 or 400 mg of MTZ for 7 days (p < .05) and 13.6% of those receiving SRP-only (p < .05). Fourteen days of MTZ + AMX was the only significant predictor of subjects reaching the clinical endpoint at 1 year (OR, 5.26; 95% CI, 2.3-12.1, p = .0000). The frequency of adverse events did not differ among treatment groups (p > .05).
The adjunctive use of 400 or 250 mg of MTZ plus 500 mg of AMX/TID/14 days offers statistically significant and clinically relevant benefits over those achieved with SRP alone in the treatment of severe GChP. The added benefits of the 7-days regimen in this population were less evident. (ClinicalTrials.gov NCT02735395).
评估不同剂量甲硝唑(MTZ)和 MTZ+阿莫西林(AMX)联合治疗时间(7 天或 14 天)对广泛性慢性牙周炎(GChP)的临床疗效。
将患有严重 GChP 的受试者随机分为仅接受牙周基础治疗(SRP)组,或联合使用 250 或 400mg MTZ+AMX(500mg),每天三次(TID),持续 7 或 14 天。受试者随访 1 年。
共纳入 109 名受试者。在 1 年时,分别有 61.9%和 63.6%接受 AMX+250 或 400mg MTZ 治疗 14 天的受试者达到了治疗的临床终点(≤4 个位点的探诊深度≥5mm),而接受 250 或 400mg MTZ 治疗 7 天的受试者分别为 31.8%(p<0.05),仅接受 SRP 的受试者为 13.6%(p<0.05)。MTZ+AMX 治疗 14 天是受试者在 1 年时达到临床终点的唯一显著预测因素(OR,5.26;95%CI,2.3-12.1,p=0.0000)。各组不良反应发生率无差异(p>0.05)。
在治疗严重 GChP 方面,与单独使用 SRP 相比,联合使用 400 或 250mg MTZ+500mg AMX/TID/14 天在统计学上和临床上均有显著获益。该人群中 7 天疗程的附加益处不太明显。(ClinicalTrials.gov NCT02735395)