青少年特发性脊柱侧凸的椎体前方系带术:我们最初十年的临床经验。

IF 1.6 Q3 CLINICAL NEUROLOGY
Spine deformity Pub Date : 2024-09-01 Epub Date: 2024-05-26 DOI:10.1007/s43390-024-00897-w
John T Braun, Sofia C Federico, David M Lawlor, Nikolaos J Paschos, Daniel P Croitoru, Brian E Grottkau
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引用次数: 0

摘要

背景:椎体前系带术(AVT)是治疗青少年特发性脊柱侧弯症(AIS)的融合手术的微创替代方法,它为脊柱侧弯症的彻底治疗提供了可能性,并能保护脊柱的生长、运动、功能和整体健康。本研究是我们使用 AVT 治疗 AIS 的第一个十年:在这项回顾性研究中,我们分析了 2010-2020 年使用 AVT 治疗的首批 74 例 AIS 患者。结果:在 74 名连续接受 AVT 治疗的 AIS 患者中,有 1 名患者的骨骼成熟度为 Risser -1 至 5:结果:在 74 名接受反向旋转手术治疗的连续 AIS 患者中,有 52 名患者(47 名女性,5 名男性)接受了为期两年的随访。这 52 名患者中有 46 人(88%)的 65 个曲线(35T、30TL/L)经 AVT 治疗后效果令人满意,曲线矫正从术前 48.6°(范围 33°-70°)(年龄 15.1 岁(范围 9.2-18.8))和骨骼成熟度 Risser 2.8(范围 -1-5)到术后 23.2°(范围 0°-54°)和随访 3.3 年(范围 2-10 年)最终 24.0°(范围 0°-49°)。从术前到术后以及从术前到最终的曲线校正均有显著意义(P 结论:AIS 在术后和最终的曲线校正均有显著意义:在这项研究中,大多数患者在不同的曲线幅度、曲线类型和骨骼成熟度下,都能通过反向旋转手术获得满意的 AIS 治疗效果。虽然因过度矫正、矫正不足或系带断裂而进行后期翻修手术的情况并不少见,但通过对适应症的改进,我们在最初的十名患者中消除了过度矫正的并发症:证据等级:IV。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Anterior vertebral tethering for adolescent idiopathic scoliosis: our initial ten year clinical experience.

Background: Anterior vertebral tethering (AVT) is a minimally invasive alternative to fusion surgery for adolescent idiopathic scoliosis (AIS) that offers the potential for definitive scoliosis treatment with the possibility of preservation of the growth, motion, function and overall health of the spine. This study represents our first ten years using AVT to treat AIS.

Methods: In this retrospective review we analyzed our first 74 AIS patients treated with AVT 2010-2020. Multiple Lenke curve types 33-70° were treated with skeletal maturity spanning Risser -1 to 5.

Results: Of 74 consecutive AIS patients treated with AVT, 52 patients (47 female, 5 male) had sufficient 2-year follow-up for inclusion. Forty-six of these 52 patients (88%) with 65 curves (35T, 30TL/L) were satisfactorily treated with AVT demonstrating curve correction from 48.6° pre-op (range 33°-70°) at age 15.1 years (range 9.2-18.8) and skeletal maturity of Risser 2.8 (range -1 to 5) to 23.2° post-op (range 0°-54°) and 24.0° final (range 0°-49°) at 3.3 years follow-up (range 2-10 years). Curve corrections from pre-op to post-op and pre-op to final were both significant (p < 0.001). The 0.8° change from post-op to final was not significant but did represent good control of scoliosis correction over time. Thoracic kyphosis and lumbar lordosis were maintained in a normal range throughout while axial rotation demonstrated a slight trend toward improvement. Skeletal maturity of Risser 4 or greater was achieved in all but one patient. Four of the 52 patients (8%) required additional procedures for tether rupture (3 replacements) or overcorrection (1 removal) to achieve satisfactory treatment status after AVT. An additional 6 of the 52 patients (12%), however, were not satisfactorily treated with AVT, requiring fusion for overcorrection (2) or inadequate correction (4).

Conclusions: In this study, AIS was satisfactorily treated with AVT in the majority of patients over a broad range of curve magnitudes, curve types, and skeletal maturity. Though late revision surgery for overcorrection, inadequate correction, or tether rupture was not uncommon, the complication of overcorrection was eliminated after our first ten patients by a refinement of indications.

Level of evidence: IV.

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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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