Trueness evaluation of three intraoral scanners for the recording of maximal intercuspal position.

Siyu Wang, Zheqing Zhou, Quan Yuan, Li Yue, Shengtao Yang
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Abstract

OBJECTIVES This clinical study aimed to assess the trueness of three intraoral scanners for the recor-ding of the maximal intercuspal position (MIP) to provide a reference for clinical practice. METHODS Ten participants with good occlusal relationship and healthy temporomandibular joint were recruited. For the control group, facebow transferring procedures were performed, and bite registrations at the MIP were used to transfer maxillary and mandibular casts to a mechanical articulator, which were then scanned with a laboratory scanner to obtain digital cast data. For the experimental groups, three intraoral scanners (Trios 3, Carestream 3600, and Aoralscan 3) were used to obtain digital casts of the participants at the MIP following the scanning workflows endorsed by the corresponding manufacturers. Subsequently, measurement points were marked on the control group's digital casts at the central incisors, canines, and first molars, and corresponding distances between these points on the maxillary and mandibular casts were measured to calculate the sum of measured distances (DA). Distances between measurement points in the incisor (DI), canine (DC), and first molar (DM) regions were also calculated. The control group's maxillary and mandibular digital casts with the added measurement points were aligned with the experimental group's casts, and DA, DI, DC, and DM values of the aligned control casts were determined. Statistical analysis was performed on DA, DI, DC, and DM obtained from both the control and experimental groups to evaluate the trueness of the three intraoral scanners for the recording of MIP. RESULTS In the control group, DA, DI, DC, and DM values were (39.58±6.40), (13.64±3.58), (14.91±2.85), and (11.03±1.56) mm. The Trios 3 group had values of (38.99±6.60), (13.42±3.66), (14.55±2.87), and (11.03±1.69) mm. The Carestream 3600 group showed values of (38.57±6.36), (13.56±3.68), (14.45±2.85), and (10.55±1.41) mm, while the Aoralscan 3 group had values of (38.16±5.69), (13.03±3.54), (14.23±2.59), and (10.90±1.54) mm. Analysis of variance revealed no statistically significant differences between the experimental and control groups for overall deviation DA (P=0.96), as well as local deviations DI (P=0.98), DC (P=0.96), and DM (P=0.89). CONCLUSIONS With standardized scanning protocols, the three intraoral scanners demonstrated comparable trueness to traditional methods in recording MIP, fulfilling clinical requirements.
对三种口内扫描仪记录最大牙间隙位置的真实性进行评估。
方法招募了十名咬合关系良好、颞下颌关节健康的参与者作为对照组。对照组进行面弓转移术,在MIP处进行咬合记录,将上颌和下颌铸模转移到机械关节器上,然后用实验室扫描仪对铸模进行扫描,获得数字化铸模数据。实验组则使用三台口内扫描仪(Trios 3、Carestream 3600 和 Aoralscan 3),按照相应制造商认可的扫描工作流程,在 MIP 处获取参与者的数字化模型。随后,在对照组的数字铸模上的中切牙、犬齿和第一磨牙处标记测量点,并测量上颌和下颌铸模上这些点之间的相应距离,以计算测量距离总和(DA)。此外,还计算了门齿(DI)、犬齿(DC)和第一磨牙(DM)区域测量点之间的距离。将添加了测量点的对照组上颌和下颌数字铸模与实验组铸模对齐,并确定对齐后的对照组铸模的 DA、DI、DC 和 DM 值。结果 对照组的 DA、DI、DC 和 DM 值分别为(39.58±6.40)、(13.64±3.58)、(14.91±2.85)和(11.03±1.56)mm。Trios 3 组的数值为(38.99±6.60)、(13.42±3.66)、(14.55±2.87)和(11.03±1.69)毫米。Carestream 3600 组的数值为(38.57±6.36)、(13.56±3.68)、(14.45±2.85)和(10.55±1.41)毫米,而 Aoralscan 3 组的数值为(38.16±5.69)、(13.03±3.54)、(14.23±2.59)和(10.90±1.54)毫米。方差分析显示,实验组和对照组在总体偏差 DA(P=0.96)以及局部偏差 DI(P=0.98)、DC(P=0.96)和 DM(P=0.89)方面无显著统计学差异。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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