Department of Periodontology, Academic Centre for Dentistry Amsterdam, Amsterdam, The Netherlands.
J Clin Periodontol. 2012 Dec;39(12):1159-65. doi: 10.1111/jcpe.12007. Epub 2012 Oct 21.
Various laser systems are currently available for intra-oral use. Neodymium:Yttrium-Aluminium Garnet lasers(Nd:YAG) have been approved by the US Food and Drug Administration for soft tissue treatment in the oral cavity.
The aim of this study was to test whether the use of a water-cooled Nd:YAG laser during a maintenance care programme as an adjunct to supragingival and subgingival debridement (scaling and root planing, SRP) with hand and ultrasonic instruments results in clinical improvement compared with SRP alone.
This study was an examiner-blind, randomized and controlled clinical trial using a split-mouth design. Thirty subjects were selected, originally diagnosed with moderate to severe generalized periodontitis, following a periodontal maintenance care programme (PMC). Immediately after SRP in two randomly assigned contra-lateral quadrants, all pockets ≥5 mm were additionally treated with a Nd:YAG laser (1064 nm, 4W, 250-μsec pulse). Clinical assessments [probing pocket depth PPD, bleeding on pocket probing (BOPP)] were performed pre-treatment and at 6 months. Based on these assessments, the periodontal inflamed surface area (PISA) was calculated.
At 6 months, the clinical parameters had significantly improved for both regimens. No statistically significant differences between treatment modalities were observed for PPD and BOPP scores at any time. PISA scores supported these findings.
In residual pockets ≥5 mm, treated in a PMC, the adjunctive use of an Nd:YAG laser does not provide a clinically significant additional advantage.
目前有多种激光系统可用于口腔内使用。钕:钇铝石榴石激光(Nd:YAG)已获得美国食品和药物管理局批准,可用于口腔软组织治疗。
本研究旨在测试在维持性护理计划中使用水冷 Nd:YAG 激光作为龈上和龈下清创(刮治和根面平整,SRP)的辅助手段,与单独使用 SRP 相比,是否会导致临床改善。
这是一项 examiner-blind、随机对照临床试验,采用 split-mouth 设计。选择 30 名最初被诊断为中重度广泛性牙周炎的受试者,在接受牙周维持性护理计划(PMC)后。在随机分配的两个对侧象限中,所有≥5mm 的袋均在 SRP 后立即用 Nd:YAG 激光(1064nm,4W,250-μsec 脉冲)进行额外治疗。临床评估[探诊袋深度 PPD、探诊袋出血(BOPP)]在治疗前和 6 个月进行。基于这些评估,计算了牙周炎表面面积(PISA)。
在 6 个月时,两种治疗方案的临床参数均显著改善。在任何时候,两种治疗方法的 PPD 和 BOPP 评分均无统计学差异。PISA 评分支持这些发现。
在 PMC 中治疗的残留≥5mm 袋中,附加使用 Nd:YAG 激光并不能提供临床显著的额外优势。