Long-term photogrammetric outcomes of midface advancement in Apert syndrome: are we nearing normal?

IF 1.3 4区 医学 Q4 CLINICAL NEUROLOGY Child's Nervous System Pub Date : 2024-09-13 DOI:10.1007/s00381-024-06611-5
Meagan Wu, Benjamin B. Massenburg, Dillan F. Villavisanis, Jinggang J. Ng, Dominic J. Romeo, Connor S. Wagner, Scott P. Bartlett, Jordan W. Swanson, Jesse A. Taylor
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Abstract

Background

The aesthetic goals of midface surgery in Apert syndrome are to correct the multi-planar midface deficiency and normalize facial ratios. This study characterizes the long-term photogrammetric outcomes of midface advancement in Apert syndrome.

Methods

Patients with Apert syndrome who underwent midface distraction from 2000 to 2023 were retrospectively reviewed. Soft tissue measurements were applied to preoperative (T0), short-term postoperative (T1), and long-term postoperative (T2) photographs. Long-term changes were compared between subcranial and transcranial procedures, segmental and non-segmental osteotomies, and individual techniques. Frontal facial dimensions at time T2 were compared to age- and sex-matched normal controls from the NIMH-ChEFS face database.

Results

Twenty patients had postoperative follow-up of T1 = 0.6 ± 0.4 and T2 = 4.7 ± 1.1 years and were compared to 40 normal controls. From time T0 to T2, middle facial third height increased (26.1 ± 3.0% to 27.8 ± 2.6%, p = 0.026), canthal tilt improved (− 7.6° ± 3.7° to − 3.9° ± 4.4°, p < 0.001), and facial convexity increased (182.9° ± 6.2° to 167.9° ± 8.6°, p < 0.001). From time T1 to T2, facial convexity flattened (159.4° ± 10.1° to 167.9° ± 8.6°, p < 0.001). Compared to controls, patients at time T2 had shorter middle facial third height (27.8 ± 2.6% vs. 32.0 ± 1.9%, p < 0.001) and reverse canthal tilt (− 3.9° ± 4.4° vs. 5.4° ± 2.6°, p < 0.001).

Conclusions

A tailored treatment approach to the Apert midface yields varying degrees of resolution of central midfacial shortening, canthal tilt, and facial concavity at 5 years postoperatively. A slight reduction in facial convexity over time, likely reflecting pseudorelapse in the setting of sagittal overcorrection, should be anticipated. Greater utilization of segmental osteotomies may bring facial third ratios and canthal tilt closer to normal morphometric values.

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阿博特综合征面中部前移的长期摄影测量结果:我们接近正常了吗?
背景阿博特综合征的中面部手术的美学目标是矫正多平面的中面部缺损并使面部比例正常化。本研究对阿博特综合征患者接受中面牵引术的长期摄影测量结果进行了分析。方法回顾性分析了 2000 年至 2023 年期间接受中面牵引术的阿博特综合征患者。对术前(T0)、术后短期(T1)和术后长期(T2)照片进行软组织测量。比较了颅下手术和经颅手术、分段截骨和非分段截骨以及不同技术之间的长期变化。结果20名患者的术后随访时间分别为T1 = 0.6 ± 0.4年和T2 = 4.7 ± 1.1年,并与40名正常对照组进行了比较。从 T0 到 T2,面部中间三分之一高度增加(26.1 ± 3.0% 到 27.8 ± 2.6%,p = 0.026),眼轮匝肌倾斜度改善(- 7.6° ± 3.7° 到 - 3.9° ± 4.4°,p <0.001),面部凸度增加(182.9° ± 6.2° 到 167.9° ± 8.6°,p <0.001)。从 T1 时间到 T2 时间,面部凸度变平(159.4° ± 10.1° 到 167.9° ± 8.6°,p < 0.001)。与对照组相比,患者在 T2 时的面中部三分之一高度较短(27.8 ± 2.6% vs. 32.0 ± 1.9%,p < 0.001),并且面颊部反向倾斜(- 3.9° ± 4.4° vs. 5.4° ± 2.6°,p < 0.001)。随着时间的推移,面部凸度会略有下降,这可能反映了矢状面过度矫正过程中的假性下垂。更多地使用节段截骨术可能会使面部三分之一比率和眼窝倾斜度更接近正常形态测量值。
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来源期刊
Child's Nervous System
Child's Nervous System 医学-临床神经学
CiteScore
3.00
自引率
7.10%
发文量
322
审稿时长
3 months
期刊介绍: The journal has been expanded to encompass all aspects of pediatric neurosciences concerning the developmental and acquired abnormalities of the nervous system and its coverings, functional disorders, epilepsy, spasticity, basic and clinical neuro-oncology, rehabilitation and trauma. Global pediatric neurosurgery is an additional field of interest that will be considered for publication in the journal.
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