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LeFort I 截骨术(上颌骨前徙术)联合或不联合 ANS 降低术治疗 III 类骨骼畸形患者后鼻侧轮廓的变化:一项随机临床试验研究方案。

Nasal profile changes after LeFort I osteotomy (maxillary advancement) with and without ANS reduction in class III skeletal patients: a study protocol for a randomized clinical trial.

机构信息

Department of Oral and Maxillofacial Surgery, Dental Faculty, Tehran Medical Sciences, Islamic Azad University, Tehran, Iran.

Tehran Medical Sciences, Islamic Azad University, Tehran, Iran.

出版信息

Trials. 2024 May 27;25(1):346. doi: 10.1186/s13063-024-08162-1.

Abstract

BACKGROUND

Dentofacial malformation is a common condition that affects a significant portion of the population, resulting in functional and aesthetic defects. Orthognathic surgeries, such as LeFort I osteotomy, are performed to correct these abnormalities. However, the impact of these surgeries on nasal profile changes remains unclear. Additionally, the role of anterior nasal spine (ANS) reduction in maxillary advancement surgeries of 3-5 mm range is yet to be determined. This study aims to investigate the effect of ANS reduction on soft tissue profile changes following LeFort I osteotomy with a maxillary advancement range of 3-5 mm in class III skeletal patients. The hypothesis is that the changes in nasolabial angle and upper lip length will not significantly differ between patients who undergo LeFort I osteotomy with and without ANS reduction.

METHOD AND DESIGN

This study is designed as a randomized controlled trial. A total of 26 class III skeletal patients with maxillofacial abnormalities will be recruited from the maxillofacial clinic of Bu-Ali and Farahikhtegan Hospitals in Tehran, Iran. Patients meeting the inclusion criteria will be randomly assigned to two groups: one group will undergo LeFort I osteotomy with ANS reduction, and the other group will undergo LeFort I osteotomy without ANS reduction. The soft tissue profile changes, specifically the nasolabial angle and upper lip length, will be evaluated and compared between the two groups.

DISCUSSION

Achieving facial harmony through orthognathic surgery requires careful planning and consideration of the impact on surrounding soft tissue. The primary objective is to predict and plan for the effects on the nasolabial region. LeFort I osteotomy is a common procedure used to correct dentofacial deformities, particularly in class III patients. Maxillary advancement during this surgery can lead to changes in nasal tip position, width, and rotation, potentially due to repositioning of the anterior nasal spine and soft tissue dissection. In this study, soft tissue changes will be assessed in non-growing class III patients using cephalometric radiographs. The impact of reducing the anterior nasal spine (ANS) on nasal profile changes will be investigated for maxillary advancements of 3-5 mm. Objective measurements and patient-reported outcomes will be evaluated to gain insights into the aesthetic outcomes of orthognathic surgery. The findings will provide valuable guidance for treatment decisions and alternative options based on expected nasal profile changes.

TRIAL REGISTRATION

This project was registered at The Iranian Registry of Clinical Trials (Identifier No. IRCT20210928052625N1, Website: https://www.irct.ir/trial/59171 ) and Open Science Framework (OSF) (Registration https://doi.org/10.17605/OSF.IO/X3HD4 ). 2021-06-09.

摘要

背景

牙颌面畸形是一种常见病症,影响着相当一部分人群,导致其出现功能和美学缺陷。正颌手术,如 LeFort I 截骨术,被用于矫正这些畸形。然而,这些手术对上颌前突 3-5mm 范围内的鼻轮廓变化的影响仍不清楚。此外,在前鼻棘(ANS)减少在 3-5mm 范围内上颌骨前徙手术中的作用尚未确定。本研究旨在探讨 LeFort I 截骨术结合上颌骨前徙 3-5mm 范围内的 ANS 减少对 III 类骨骼患者软组织轮廓变化的影响。假设接受 LeFort I 截骨术联合和不联合 ANS 减少的患者,其鼻唇角和上唇长度的变化没有显著差异。

方法和设计

本研究设计为随机对照试验。总共将从伊朗德黑兰的 Bu-Ali 和 Farahikhtegan 医院的颌面诊所招募 26 名具有颌面畸形的 III 类骨骼患者。符合纳入标准的患者将被随机分配到两组:一组患者将接受 LeFort I 截骨术联合 ANS 减少,另一组患者将接受 LeFort I 截骨术不联合 ANS 减少。将评估和比较两组之间的软组织轮廓变化,特别是鼻唇角和上唇长度。

讨论

通过正颌手术实现面部和谐需要精心规划和考虑对周围软组织的影响。主要目标是预测和计划对鼻唇区域的影响。LeFort I 截骨术是一种用于矫正牙颌面畸形的常用手术,特别是在 III 类患者中。在该手术中上颌骨前徙会导致鼻尖位置、宽度和旋转的改变,这可能是由于前鼻棘和软组织解剖的重新定位所致。在本研究中,使用头颅侧位片评估非生长 III 类患者的软组织变化。将研究上颌骨前徙 3-5mm 时减少前鼻棘(ANS)对上颌前突的影响。将评估客观测量和患者报告的结果,以深入了解正颌手术的美学效果。研究结果将为治疗决策和基于预期鼻轮廓变化的替代方案提供有价值的指导。

试验注册

本项目在伊朗临床试验注册中心(注册号:IRCT20210928052625N1,网站:https://www.irct.ir/trial/59171)和开放科学框架(OSF)(注册:https://doi.org/10.17605/OSF.IO/X3HD4)进行注册。2021-06-09。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ddd2/11129358/51dca7fa6674/13063_2024_8162_Fig1_HTML.jpg

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