Differences in spine growth potential for Sanders maturation stages 7A and 7B have implications for treatment of idiopathic scoliosis.

IF 1.6 Q3 CLINICAL NEUROLOGY Spine deformity Pub Date : 2024-05-01 Epub Date: 2024-02-19 DOI:10.1007/s43390-024-00829-8
Yusuke Hori, Burak Kaymaz, Luiz Carlos Almeida da Silva, Kenneth J Rogers, Petya K Yorgova, Peter G Gabos, Suken A Shah
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Abstract

Purpose: This study aimed to clarify the differences in spine and total body height growth and curve progression between Sanders maturation stage (SMS) 7A and 7B in patients with adolescent idiopathic scoliosis (AIS).

Methods: This retrospective case-control study involving patients with AIS at SMS 7 evaluated the differential gains in the spine (T1-S1) and total body height and curve progression between SMS 7A and 7B. A validated formula was used to calculate the corrected height, accounting for height loss due to scoliosis. A multivariable non-linear and logistic regression model was applied to assess the distinct growth and curve progression patterns between the SMS 7 subtypes, adjusting for potential confounders.

Results: A total of 231 AIS patients (83% girls, mean age 13.9 ± 1.2 years) were included, with follow-up averaging 3.0 years. Patients at SMS 7A exhibited larger gains in spine height (9.9 mm vs. 6.3 mm) and total body height (19.8 mm vs. 13.4 mm) compared with SMS 7B. These findings remained consistent even after adjustments for curve magnitude. Non-linear regression models showed continued spine and total body height increases plateauing after 2 years, significantly greater in SMS 7A. More SMS 7A patients had curve progression over 10°, with an adjusted odds ratio of 3.31.

Conclusion: This study revealed that patients staged SMS 7A exhibited more spine and total body growth and a greater incidence of substantial curve progression than those at 7B. These findings imply that delaying brace discontinuation until reaching 7B could be beneficial, particularly for those with larger curves.

Level of evidence: Level III (Case-control study).

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桑德斯成熟阶段 7A 和 7B 的脊柱生长潜力差异对特发性脊柱侧凸的治疗具有重要意义。
目的:本研究旨在阐明青少年特发性脊柱侧弯症(AIS)患者在桑德斯成熟阶段(SMS)7A和7B之间脊柱和全身身高增长及曲线进展的差异:这项回顾性病例对照研究涉及SMS 7期的特发性脊柱侧弯症患者,评估了SMS 7A和7B期患者脊柱(T1-S1)和全身身高的不同增长以及曲线进展情况。研究采用了一个经过验证的公式来计算校正身高,其中考虑了脊柱侧弯造成的身高损失。采用多变量非线性和逻辑回归模型评估 SMS 7 亚型之间不同的生长和曲线进展模式,并对潜在的混杂因素进行调整:共纳入231名AIS患者(83%为女孩,平均年龄(13.9 ± 1.2)岁),平均随访3.0年。与 SMS 7B 相比,SMS 7A 患者的脊柱高度(9.9 毫米对 6.3 毫米)和全身高度(19.8 毫米对 13.4 毫米)增长幅度更大。即使对曲线幅度进行调整后,这些结果仍保持一致。非线性回归模型显示,脊柱和全身高度在 2 年后继续增加,并趋于平稳,而 SMS 7A 的增幅明显更大。更多 SMS 7A 患者的曲线发展超过 10°,调整后的几率比为 3.31:本研究显示,SMS 7A 分期患者的脊柱和全身生长速度快于 SMS 7B 分期患者,且出现大幅度弯度进展的几率更高。这些研究结果表明,将支具停用时间推迟到 7B 阶段可能是有益的,尤其是对于那些曲线较大的患者:证据等级:三级(病例对照研究)。
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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.
期刊最新文献
Goldenhar syndrome associated with increased risk of respiratory failure and reoperations following spinal deformity surgery. Delayed neurological deficit due to a medially misplaced thoracic pedicle screw during adolescent idiopathic scoliosis correction: a complication 6 years in the making. Correction: Surgical outcome of scoliosis in patients with Marfan syndrome. Editorial. Historical perspectives-Eduardo R. Luque.
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