Comparable rates of lumbar disc degeneration at long-term following adolescent idiopathic scoliosis spinal fusion extended to L3 or L4: systematic review and meta-analysis.

IF 1.6 Q3 CLINICAL NEUROLOGY Spine deformity Pub Date : 2024-07-01 Epub Date: 2024-03-28 DOI:10.1007/s43390-024-00849-4
Alberto Ruffilli, Matteo Traversari, Marco Manzetti, Giovanni Viroli, Elena Artioli, Simone Ottavio Zielli, Antonio Mazzotti, Cesare Faldini
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引用次数: 0

Abstract

Purpose: Surgical treatment of adolescent idiopathic scoliosis (AIS) requires a careful choice of fusion levels. The usual recommendation for the selection of the lowest instrumented vertebra (LIV) for double major or thoracolumbar/lumbar (TL/L) curves falls on L3 or L4. The aim of the present study is to assess if the spinal fusion with LIV selection of L3 or L4 in AIS patients has a clinical or radiological impact in terms of degenerative disc disease (DDD) in distal unfused segments at long-term follow-up.

Methods: A systematic search of electronic databases from eligible articles was conducted. Only studies regarding long-term follow-up of AIS patients treated with spinal fusion were included. Clinical and radiographic outcomes were extracted and summarized. Meta-analysis on long-term follow-up MRI studies was performed. p value < 0.05 was considered significant.

Results: Fourteen studies were included, for a total of 1264 patients. Clinical assessment of included patients showed a slight tendency to have worse clinical outcomes if spinal fusion is extended to L4 rather than L3. Despite that, meta-analysis could not be performed on clinical parameters because of heterogeneity of evaluated PROMs in included studies. Magnetic resonance imaging (MRI) evaluation at long-term follow-up showed no significant difference in terms of disc degeneration rate at overall meta-analysis (p = 0.916) between patients fused to L3 and L4.

Conclusion: The LIV selection of L3 rather than L4, according to current literature, does not prevent disc degeneration in distal unfused segments over the long term. Long-term studies of patients treated with contemporary spinal instrumentation are needed.

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青少年特发性脊柱侧凸脊柱融合术延伸至 L3 或 L4 后,长期腰椎间盘变性的发生率相当:系统综述和荟萃分析。
目的:青少年特发性脊柱侧凸(AIS)的手术治疗需要谨慎选择融合水平。对于双大弯或胸腰椎/腰椎(TL/L)弯,通常建议选择最低的器械椎体(LIV),即 L3 或 L4。本研究旨在评估 AIS 患者选择 L3 或 L4 作为最低器械椎体的脊柱融合术在长期随访中是否会对远端未融合节段的椎间盘退行性病变(DDD)产生临床或放射学影响:方法:对电子数据库中符合条件的文章进行了系统检索。方法:对电子数据库中符合条件的文章进行了系统性检索,仅纳入了对接受脊柱融合术治疗的 AIS 患者进行长期随访的研究。提取并总结了临床和影像学结果。对长期随访的 MRI 研究进行了 Meta 分析:共纳入 14 项研究,共计 1264 例患者。对纳入研究的患者进行的临床评估显示,如果脊柱融合术延伸至 L4 而不是 L3,则临床结果略有恶化趋势。尽管如此,由于纳入研究的 PROMs 评估存在异质性,因此无法对临床参数进行荟萃分析。长期随访的磁共振成像(MRI)评估显示,在总体荟萃分析中,L3和L4融合患者的椎间盘退变率无显著差异(P = 0.916):结论:根据目前的文献,LIV选择L3而非L4并不能防止远端未融合节段的椎间盘长期退化。需要对使用现代脊柱器械治疗的患者进行长期研究。
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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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