Direct versus fully digital indirect bracket bonding: a split-mouth randomized clinical trial on accuracy

支架 医学 随机对照试验 临床试验 口腔正畸科 临床意义 牙科 物理疗法 外科 内科学 结构工程 工程类
作者
Pauline M J Hoekstra-van Hout,J. Hoekstra,Robin Bruggink,Ewald M. Bronkhorst,Edwin M. Ongkosuwito
出处
期刊:Clinical Oral Investigations [Springer Nature]
卷期号:28 (10)
标识
DOI:10.1007/s00784-024-05950-6
摘要

Abstract Objectives The primary aim is to assess differences in accuracy of orthodontic bracket positioning between fully digital indirect bracket bonding (IDB) and conventional direct bracket bonding (DBB). The secondary aims are to assess differences in bracket bonding failures, bracket repositioning need, clinician experience and patient satisfaction. Materials and methods This prospective study was designed as a split-mouth randomized clinical trial. In total, 35 patients were analyzed with a six month follow-up period. Translational and orientational deviations from the planned bracket position were determined. Clinician experience and patient satisfaction were evaluated by means of a survey. Results The difference in translation was 0.34 mm (95% CI: 0.238–0.352, p = 0.017), the difference in orientation was 4.80˚ (95% CI: 3.858–5.727, p < 0.001), both in favour of IDB. IDB showed significantly more immediate (IDB: 3.9%, DBB: 0%) and late (IDB: 5.4%, DBB: 2.5%, p = 0.008) bonding failures. Clinicians and patients experienced a shorter clinical chair time with indirect bonding over direct bonding. Conclusions IDB bracket positioning leads to significant smaller translation and orientation deviations from digital IDB planning, than DBB bracket positioning. However, IDB leads to more immediate bonding failures than DBB. The majority of patients preferred IDB over DBB, due to a shorter clinical chair time. Clinical relevance This study adds to the knowledge of IDB in orthodontics and contributes to evidence on this technique. This evidence is applicable in everyday orthodontics, with respect to patient satisfaction and technical limits of IDB. The trial was registered in the Dutch Trial Register and the International Clinical Trials Registry Platform (ICTRP) of the World Health Organization (WHO), number NL9411.
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