基于移动设备的3D扫描在评估青少年特发性脊柱侧凸方面优于脊柱侧凸计。

IF 1.6 Q3 CLINICAL NEUROLOGY
Yousi Oquendo, Ian Hollyer, Clayton Maschhoff, Christian Calderon, Malcolm DeBaun, Joanna Langner, Nadine Javier, Xochitl Bryson, Ann Richey, Hiba Naz, Kali Tileston, Michael Gardner, John S Vorhies
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引用次数: 0

摘要

目的:青少年特发性脊柱侧凸(AIS)的筛查目前依赖于训练有素的从业人员的临床评估,最常用的是使用脊柱侧凸计。现代结构光3D扫描可以使用移动设备生成高质量的表面解剖3D表示。我们假设,与脊柱侧弯计相比,基于移动的3D扫描系统可以提供准确的畸形评估。方法:纳入2020年8月至2022年6月期间在我们诊所接受AIS评估的10-18岁患者,这些患者在临床评估后30天内获得脊柱侧凸x线片,无脊柱手术史。患者在直立和前屈位置进行3D扫描,并通过脊柱侧弯计测量躯干旋转的最大角度(ATR)。采用图像处理软件分析直立体位的躯干位移(TS)、冠状平衡(CB)、锁骨角(CL)以及前屈体位的最大ATR。三维和脊柱侧弯测量与主要曲线的大小相关。在控制人口统计协变量的情况下,基于3D和脊柱侧弯仪测量创建了多个逻辑回归模型。结果:258例患者纳入本研究。平均冠状动脉大弯曲幅度为25.7°(范围0-100),59%为胸大弯曲。TS、CB和CL的3D和影像学测量之间存在良好到极好的相关性(r = 0.79, rs = 0.80和r = 0.64)。结论:在该人群中,基于移动设备的TS、CB和TS 3D扫描可识别临床相关的脊柱侧凸畸形,并且比脊柱侧凸计更能预测影像学曲线大小。这种新模式可以通过减少对训练有素的人员或专用设备和临床空间进行筛查试验的需求来促进脊柱侧凸筛查。证据水平:II。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Mobile device-based 3D scanning is superior to scoliometer in assessment of adolescent idiopathic scoliosis.

Purpose: Screening for adolescent idiopathic scoliosis (AIS) currently relies on clinical evaluations by trained practitioners, most commonly using a scoliometer. Modern structured light 3D scanning can generate high-quality 3D representations of surface anatomy using a mobile device. We hypothesized that a mobile-based 3D scanning system would provide accurate deformity assessments compared to a scoliometer.

Methods: Between August 2020 and June 2022, patients 10-18 years being evaluated for AIS in our clinic with a scoliosis radiograph obtained within 30 days of clinic evaluation and no history of spinal surgery were enrolled. Patients had 3D scans taken in the upright and forward bend positions, and the largest angle of trunk rotation (ATR) was measured by a scoliometer. Image processing software was used to analyze trunk shift (TS), coronal balance (CB), and clavicle angle (CL) in the upright position and the largest ATR in the forward bend position. 3D and scoliometer measurements were correlated to major curve magnitude. Multiple logistic regression models were created based on 3D and scoliometer measurements, controlling for demographic covariates.

Results: Two hundred and fifty-eight patients were included in this study. Mean coronal major curve magnitude was 25.7° (range 0-100), and 59% had a thoracic major curve. There were good-to-excellent correlations between 3D and radiographic measures of TS, CB, and CL (r = 0.79, rs = 0.80, and r = 0.64, respectively, p < 0.001). Correlations between 3D and radiographic measures of largest lumbar and thoracic ATR also demonstrated good correlations (r = 0.64 for both, p < 0.001). Using Akaike's Information Criterion (AIC), a multivariable logistic regression model based on 3D scanning outperformed a scoliometer model.

Conclusions: Mobile device-based 3D scanning of TS, CB, and TS identifies clinically relevant scoliotic deformity and is more predictive of radiographic curve magnitude than scoliometer in this population. This new modality may facilitate scoliosis screening by decreasing the need for trained personnel or dedicated equipment and clinical space to perform screening tests.

Level of evidence: II.

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来源期刊
CiteScore
3.20
自引率
18.80%
发文量
167
期刊介绍: Spine Deformity the official journal of the?Scoliosis Research Society is a peer-refereed publication to disseminate knowledge on basic science and clinical research into the?etiology?biomechanics?treatment?methods and outcomes of all types of?spinal deformities. The international members of the Editorial Board provide a worldwide perspective for the journal's area of interest.The?journal?will enhance the mission of the Society which is to foster the optimal care of all patients with?spine?deformities worldwide. Articles published in?Spine Deformity?are Medline indexed in PubMed.? The journal publishes original articles in the form of clinical and basic research. Spine Deformity will only publish studies that have institutional review board (IRB) or similar ethics committee approval for human and animal studies and have strictly observed these guidelines. The minimum follow-up period for follow-up clinical studies is 24 months.
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