Flores-Mir Carlos
School of Dentistry, University of Alberta, Edmonton, AB, Canada.
Evid Based Dent. 2024 Sep;25(3):136-137. doi: 10.1038/s41432-024-01038-y. Epub 2024 Jul 30.
The Cochrane Central Register of Controlled Trials (CENTRAL), PubMed, Scopus, Web of Science, Google Scholar, Trip, CINAHL via EBSCO, EMBASE via OVID and ProQuest searched up to June 2023. Any clinical study with parallel arms and matched malocclusion severity should include permanent dentition participants with mild to mild-to-moderate anterior crowding. Participants should have undergone orthodontic treatment with either orthodontic labial fixed appliances or removable clear aligners. Total treatment time (primary outcome), chair time, number of appointments, and emergency visits (secondary outcomes) should also be reported.
Two reviewers selected the studies to be considered in two stages. If needed, a third reviewer was included to solve discrepancies. Endnote and Rayyan software supported the process.
The same two reviewers independently extracted the required data from the included studies. If needed, a third reviewer was included to solve discrepancies. Endnote and Rayyan software supported the process.
Ten studies were finally included (six RCTs and four non-RCTs). Only one included samples in which teeth were extracted due to crowding. The total included sample was 718 participants (aged 20-29 years). Only one study did not report crowding equivalency between groups.
Based on low to very low certainty levels, treatment duration is likely similar, chair time and emergency visits are less frequent, and the number of appointments is increased with clear aligners.
截至2023年6月,检索了Cochrane对照试验中央注册库(CENTRAL)、PubMed、Scopus、科学网、谷歌学术、Trip、通过EBSCO检索的护理学与健康领域数据库(CINAHL)、通过OVID检索的EMBASE以及ProQuest。任何具有平行组且错牙合严重程度匹配的临床研究均应纳入恒牙列、有轻度至轻度到中度前牙拥挤的参与者。参与者应接受过正畸唇侧固定矫治器或可摘式透明矫治器的正畸治疗。还应报告总治疗时间(主要结局)、椅旁时间、预约次数和急诊就诊次数(次要结局)。
两名评审员分两个阶段选择要纳入的研究。如有需要,纳入第三名评审员以解决分歧。Endnote和Rayyan软件辅助该过程。
同样由这两名评审员独立从纳入研究中提取所需数据。如有需要,纳入第三名评审员以解决分歧。Endnote和Rayyan软件辅助该过程。
最终纳入10项研究(6项随机对照试验和4项非随机对照试验)。只有1项研究纳入了因拥挤而拔牙的样本。纳入的样本总数为718名参与者(年龄在20 - 29岁之间)。只有1项研究未报告组间拥挤程度的等效性。
基于低至极低的确信度,使用透明矫治器时,治疗持续时间可能相似,椅旁时间和急诊就诊次数较少,而预约次数会增加。