Minimally-invasive lateral thoracic and lumbar interbody fusion (LLIF) with expandable interbody cages – Considerations, complications & outcomes

IF 1.9 Q3 CLINICAL NEUROLOGY Brain & spine Pub Date : 2024-01-01 DOI:10.1016/j.bas.2024.102870
Martin N. Stienen , Gregor Fischer , Linda Bättig , Anand Veeravagu , Benjamin Martens
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Abstract

Introduction

Reports about lateral lumbar or thoracic interbody fusion (LLIF) using expandable interbody spacers are sparse.

Research question

To report our experience with the use of expandable spacers for LLIF.

Material and methods

We reviewed all consecutive LLIF patients with use of an expandable titanium interbody implant (ELSA® Expandable Integrated LLIF Spacer, Globus Medical Inc, PA (USA)) between September 2018 and January 2024.

Results

We identified 503 patients, in which we performed LLIF at 732 levels. In 63 patients (12.5%) and 70 levels (9.6%) an expandable spacer was used. The mean age was 61.4 years, 57.1% were females. LLIF was performed between T11/12 – L4/5 in the setting of fusion procedures (mono-/bisegmental (20; 28.6%), 3–7 segments (29; 41.4%); >7 segments (21; 30.0%)), of which 21 (33.3%), 20 (31.8%) and 22 (34.9%) were for traumatic, deformity/revision and other diagnoses. Surgery included release of the anterior longitudinal ligament in 30 cases (42.9%). Intraoperative adverse events (AEs) were noted in 2 (3.2%), postoperative AEs in 27 (42.9%) at discharge, 17 (27.0%) at 3 months and 14 (22.2%) at 12 months. Segmental sagittal Cobb angle changed from 1.3° (preoperative) to 13.0° at discharge (p < 0.001), 12.7° at 3 months (p < 0.001) and 13.3° at 12 months (p < 0.001). Functional outcome was excellent/good in 43 (68.3%; 5 missing) at 3 months and in 37 (58.7%; 10 missing) at 12 months.

Discussion and conclusion

The use of LLIF with an expandable spacer was safe, promoted solid fusion and enabled powerful correction of sagittal segmental Cobb angle, which was maintained during follow-up.

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使用可扩张椎间融合器的微创侧胸椎和腰椎椎间融合术(LLIF)--注意事项、并发症和结果
材料和方法我们回顾了 2018 年 9 月至 2024 年 1 月期间使用可膨胀钛椎间植入物(ELSA® 可膨胀一体化 LLIF 椎间间隔,Globus Medical Inc,宾夕法尼亚州(美国))的所有连续 LLIF 患者。其中 63 例患者(12.5%)和 70 个水平(9.6%)使用了可扩张间隔器。患者平均年龄为61.4岁,57.1%为女性。LLIF手术在T11/12-L4/5之间的融合手术中进行(单节段/双节段(20例;28.6%)、3-7节段(29例;41.4%);7节段(21例;30.0%)),其中21例(33.3%)、20例(31.8%)和22例(34.9%)用于外伤、畸形/翻修和其他诊断。30例(42.9%)手术包括前纵韧带松解术。2例(3.2%)出现术中不良反应,27例(42.9%)在出院时出现术后不良反应,17例(27.0%)在3个月时出现术后不良反应,14例(22.2%)在12个月时出现术后不良反应。节段矢状面 Cobb 角度从术前的 1.3° 变为出院时的 13.0°(p <0.001)、3 个月时的 12.7°(p <0.001)和 12 个月时的 13.3°(p <0.001)。3个月时有43人(68.3%;5人缺失)的功能结果为优秀/良好,12个月时有37人(58.7%;10人缺失)的功能结果为优秀/良好。
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来源期刊
Brain & spine
Brain & spine Surgery
CiteScore
1.10
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0.00%
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审稿时长
71 days
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