Department of Orthopaedic Surgery, University Medical Center Utrecht, Utrecht, the Netherlands.
Department of Orthopaedic Surgery, University Medical Center Utrecht, Utrecht, the Netherlands.
Spine J. 2021 Apr;21(4):671-681. doi: 10.1016/j.spinee.2020.11.007. Epub 2020 Nov 20.
Current surgical treatment options for early onset scoliosis (EOS), with distraction- or growth-guidance implants, show limited growth and high complication rates during follow-up. We developed a novel implant concept, which uses compressed helical springs positioned around the rods of a growth-guidance construct. This spring distraction system (SDS) provides continuous corrective force to stimulate spinal growth, can be easily contoured, and can be used with all standard spinal instrumentation systems.
To assess curve correction and -maintenance, spinal growth, complication rate, and health-related quality of life following SDS treatment.
Prospective cohort study.
All skeletally immature EOS patients with an indication for growth-friendly surgery and without bone- or soft tissue weakness were eligible to receive SDS. For this study, all included patients with at least 2-year follow-up were analyzed.
Coronal Cobb angle, sagittal parameters, T1-T12, T1-S1, and instrumented (ie, bridged segment) spinal height and freehand length, complications and re-operations, and the 24-Item Early Onset Scoliosis Questionnaires (EOSQ-24) score.
All primary- and conversion patients (conversion from failed other systems) with SDS and ≥2 years follow-up were included. Radiographic parameters were compared preoperatively, postoperatively and at latest follow-up. Spinal length increase was expressed as mm/year.
Twenty-four skeletally immature EOS patients (18 primary and 6 conversion cases) were included. There were five idiopathic, seven congenital, three syndromic, and nine neuromuscular EOS patients. Mean age at implantation was 9.1 years (primary: 8.4; conversion: 11.2). Major curve improved from 60.3° to 35.3°, and was maintained at 40.6° at latest follow-up. Mean spring length increase during follow-up was 10.4 mm/year. T1-S1 height increased 9.9mm/year and the instrumented segment height showed a mean increase of 0.7 mm/segment/year. EOSQ-24 scores dropped after surgery from 75.6 to 67.4 but recovered to 75.0 at latest follow-up. In total, 17 reoperations were performed. Ten reoperations were performed to treat 9 implant-related complications. In addition, 7 patients showed spinal growth that exceeded expected growth velocity; their springs were retensioned during a small reoperation.
The 2-year follow-up results from this prospective cohort study indicate that the concept of spring distraction may be feasible as an alternative to current growing spine solutions. Curve correction and growth could be maintained satisfactory without the need for repetitive lengthening procedures. However, as in all growth-friendly implants, complications and reoperations could not be prevented, which emphasizes the need for further improvement.
目前用于早发性脊柱侧凸(EOS)的手术治疗选择,包括使用牵引或生长导向植入物,在随访过程中显示出有限的生长和高并发症发生率。我们开发了一种新型植入物概念,该概念使用围绕生长导向结构的棒材定位的压缩螺旋弹簧。这种弹簧牵引系统(SDS)提供持续的矫正力以刺激脊柱生长,可以轻松塑形,并可与所有标准脊柱器械系统一起使用。
评估 SDS 治疗后曲线矫正和维持、脊柱生长、并发症发生率和健康相关生活质量。
前瞻性队列研究。
所有骨骼未成熟的 EOS 患者,均有生长友好型手术指征,且无骨骼或软组织薄弱,均有资格接受 SDS。在本研究中,对所有至少有 2 年随访的纳入患者进行了分析。
冠状 Cobb 角、矢状参数、T1-T12、T1-S1、器械(即桥接节段)脊柱高度和徒手长度、并发症和再手术以及 24 项早发性脊柱侧凸问卷(EOSQ-24)评分。
所有接受 SDS 治疗且随访时间≥2 年的原发性和转换患者(从其他系统失败的病例中转换)均被纳入。术前、术后和最新随访时比较影像学参数。脊柱长度增加以毫米/年表示。
共纳入 24 例骨骼未成熟的 EOS 患者(原发性 18 例,转换病例 6 例)。其中特发性 5 例,先天性 7 例,综合征 3 例,神经肌肉性 9 例。植入时的平均年龄为 9.1 岁(原发性:8.4 岁;转换:11.2 岁)。主要曲线从 60.3°改善至 35.3°,并在最新随访时维持在 40.6°。随访期间,弹簧长度平均增加 10.4 毫米/年。T1-S1 高度增加 9.9 毫米/年,器械节段高度平均每年增加 0.7 毫米/节段。EOSQ-24 评分在手术后从 75.6 降至 67.4,但在最新随访时恢复至 75.0。共进行了 17 次再手术。10 次再手术用于治疗 9 例与植入物相关的并发症。此外,7 名患者的脊柱生长速度超过预期,他们的弹簧在小手术中被重新固定。
这项前瞻性队列研究的 2 年随访结果表明,弹簧牵引的概念可能是当前生长脊柱解决方案的一种可行替代方案。无需重复延长手术即可维持满意的曲线矫正和生长。然而,与所有生长友好型植入物一样,并发症和再手术无法避免,这强调了需要进一步改进。