Rahman Shahla, Spencer R James, Littlewood Simon J, O'Dywer Lian, Barber Sophy K, Russell Joanne S
a Specialist Orthodontist, Private Practice, Howard Marshall Dentistry, London, UK.
b Consultant Orthodontist, Pinderfields Hospital, Wakefield, UK.
Angle Orthod. 2016 Jan;86(1):149-56. doi: 10.2319/112414-838.1. Epub 2015 Mar 26.
To compare pain experience between self-ligating and conventional preadjusted edgewise appliance systems with a two-arm parallel trial.
A prospective multicenter randomized controlled clinical trial was conducted in three hospital orthodontic departments. Subjects were randomly allocated to receive treatment with either a self-ligating (3M SmartClip™) or conventional (3M Victory™) bracket system with stratification for operator and center. Standardized protocol was followed for bracket bonding procedure and archwire sequence. Subject pain was recorded using a Verbal Rating Scale to assess discomfort felt on the teeth and soft tissues at the time of the appointment and 1, 3, and 5 days after each archwire change up to the working archwire. Multilevel modeling was used to analyze the data by blinded assessors.
One hundred thirty-eight subjects (mean age 14 years 11 months) were enrolled in the study, of which 135 subjects (97.8%) completed the study and 113 (82%) returned the required data regarding pain/discomfort. Perceived pain was statistically higher with the SmartClip™ system compared to the Victory™ system, but this difference was not deemed to be clinically significant. Discomfort was greatest after placement of the initial 0.014-inch nickel-titanium archwire, compared with subsequent wires, and was greatest on day 1, less on day 3, and much less on day 5 after each archwire change. Age and gender did not affect the level of discomfort experienced by subjects undergoing fixed appliance treatment.
No clinically significant difference in pain experience was found between patients treated with a self-ligating bracket system compared to those treated with a conventional ligation system.
通过双臂平行试验比较自锁式和传统预成直丝弓矫治器系统的疼痛体验。
在三个医院的正畸科进行了一项前瞻性多中心随机对照临床试验。受试者被随机分配接受自锁式(3M SmartClip™)或传统(3M Victory™)托槽系统治疗,并按操作者和中心进行分层。托槽粘结程序和弓丝序列遵循标准化方案。使用视觉模拟评分法记录受试者的疼痛情况,以评估每次预约时以及每次更换弓丝直至工作弓丝后的第1、3和5天牙齿和软组织的不适程度。由盲法评估者使用多水平模型分析数据。
138名受试者(平均年龄14岁11个月)参与了该研究,其中135名受试者(97.8%)完成了研究,113名(82%)返回了有关疼痛/不适的所需数据。与Victory™系统相比,SmartClip™系统的疼痛感知在统计学上更高,但这种差异在临床上不被认为具有显著性。与后续弓丝相比,初始0.014英寸镍钛弓丝放置后的不适程度最大,并且在每次更换弓丝后的第1天不适程度最大,第3天减轻,第5天则大大减轻。年龄和性别不影响接受固定矫治器治疗的受试者的不适程度。
与接受传统结扎系统治疗的患者相比,接受自锁托槽系统治疗的患者在疼痛体验方面未发现临床上的显著差异。