A New Combined Protocol to Treat the Dentin Hypersensitivity Associated with Non-Carious Cervical Lesions: A Randomized Controlled Trial

被引:24
|
作者
Femiano, Felice [1 ]
Femiano, Rossella [1 ]
Femiano, Luigi [1 ]
Nucci, Ludovica [1 ]
Minervini, Giuseppe [1 ]
Antonelli, Alessandro [2 ]
Bennardo, Francesco [2 ]
Barone, Selene [2 ]
Scotti, Nicola [3 ]
Sorice, Vittoria [4 ]
Sorice, Rossella [1 ]
机构
[1] Univ Study Campania, Multidisciplinary Dept Med Surg & Dent Specialtie, Luigi Vanvitelli, Via Crecchio 6, I-83138 Naples, Italy
[2] Magna Graecia Univ Catanzaro, Sch Dent, Dept Hlth Sci, I-88100 Catanzaro, Italy
[3] Univ Turin, Dept Surg Sci, I-10125 Turin, Italy
[4] Univ Derby, Chesterfield Royal Hosp Fdn Trust, Kedleston Rd, Derby DE221 GB, England
来源
APPLIED SCIENCES-BASEL | 2021年 / 11卷 / 01期
关键词
dentin hypersensitivity; non-carious cervical lesions; diode laser; LLLT; high-power laser therapy; DIODE-LASER THERAPY; CLINICAL-EVALUATION; NDYAG LASER; ER; CR/YSGG; EFFICACY; PAIN;
D O I
10.3390/app11010187
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The goal of this research is to assess the desensitizing effect of a diode laser on non-carious cervical lesions (NCCLs) responsible for dentin hypersensitivity (DH) in two separate output forces implemented both independently and in sequential combination modalities. A randomized controlled trial for this study was applied. Sixty-nine NCCLs responsible for DH pain with severity between 6 and 9 on the VAS scale were considered. Three study groups were developed using just one lesion from three different quadrants of the oral cavity of each patient. All treatment procedures were conducted using a laser diode (810 nm, 5 W) with varying power outputs used separately or in combination. The pain by DH was evaluated at baseline, at treatment completion, and at 15 days and 3 months after each laser procedure. Data analysis was performed using a Wilcoxon test for paired samples, a one-way ANOVA test, and an unpaired t-test. The significant reduction of the mean VAS score was estimated in each study group immediately and at 15 days and 3 months after the end of treatment and compared with the baseline mean VAS score (p-value < 0.0001). The best result concerning the improvement of DH symptomatology was assessed when a combined protocol of two different output powers of the diode laser was used. The authors conclude that the diode laser (810 nm) therapy procedure combining two separate output forces (low and high power) can improve the painful symptoms of DH from NCCLs.
引用
收藏
页码:1 / 10
页数:10
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