Evans T J, Jones M L, Newcombe R G
Department of Dental Health and Development, University of Wales College of Medicine, Cardiff, UK.
Am J Orthod Dentofacial Orthop. 1998 Jul;114(1):32-9. doi: 10.1016/s0889-5406(98)70234-3.
To clinically evaluate three commonly used orthodontic tooth aligning arch wires: 016 x 022 inch active martensitic medium force nickel titanium, 016 x 022 inch graded force active martensitic nickel titanium, and 0.0155 inch multistrand stainless steel.
A prospective randomized clinical trial.
Measured serial study casts of dental arches for 112 assigned arch wires from 56 consecutive patients. Analysis based on completed records for 98 arch wires and 51 patients.
A consecutive sample of 56 patients requiring both upper and lower fixed appliance therapy were randomly allocated two different arch wires from a possible three under trial. Good quality impressions were taken of the dental arches at the designated serial stages of alignment (start, T0; 4 weeks, T4; 8 weeks, T8). The resultant casts were measured on a Reflex Microscope to record the change in individual tooth alignment both in three and two dimensions (horizontal plane only).
The measurement error was within acceptable limits (range, 0.05 to 0.09 mm) and showed no significant bias. ANOVA statistical models were fitted to the data to adjust for a number of variables. No significant difference in aligning capability (p > 0.05), in either two or three dimensions, was demonstrated between the three arch wires in the trial.
Heat activated nickel titanium arch wires failed to demonstrate a better performance than the cheaper multistrand stainless steel wires in this randomized clinical trial. The failure to demonstrate in vivo superiority at the clinical level may be due to the confounding effects of large variations in individual metabolic response. Alternatively, it may be that in routine clinical practice NiTi-type wires are not sufficiently deformed to allow their full superelastic properties to come in to play during initial alignment.
临床评估三种常用的正畸牙齿排齐弓丝:0.016×0.022英寸活性马氏体中等力量镍钛丝、0.016×0.022英寸渐变力量活性马氏体镍钛丝和0.0155英寸多股不锈钢丝。
一项前瞻性随机临床试验。
对连续56例患者的112根指定弓丝的牙弓进行测量的系列研究模型。基于98根弓丝和51例患者的完整记录进行分析。
连续抽取56例需要上下固定矫治器治疗的患者作为样本,从三种受试弓丝中随机分配两种不同的弓丝。在排齐的指定系列阶段(开始,T0;4周,T4;8周,T8)对牙弓进行高质量印模。在反射显微镜上对所得模型进行测量,以记录单个牙齿在三维和二维(仅水平面)上的排齐变化。
测量误差在可接受范围内(范围为0.05至0.09毫米),且无明显偏差。对数据拟合ANOVA统计模型以调整多个变量。试验中的三种弓丝在二维或三维排齐能力方面均未显示出显著差异(p>0.05)。
在这项随机临床试验中,热激活镍钛弓丝未能表现出比更便宜的多股不锈钢丝更好的性能。在临床水平上未能证明体内优越性可能是由于个体代谢反应的巨大差异的混杂效应。或者,可能是在常规临床实践中,镍钛型弓丝没有充分变形,以至于在初始排齐过程中无法充分发挥其完全超弹性性能。