Adjustable Lordotic Expandable Spacers: How Do They Compare to Traditional Static Spacers in Lateral Lumbar Interbody Fusion?

Y. Li, R. Frisch, Zhenggu Huang, James E. Towner, Y. Li, Amber Edsall, C. Ledonio
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Abstract

Introduction: Expandable interbody spacers with adjustable lordosis were designed to expand in situ and avoid complications such as endplate damage, excessive trialing and forceful impaction associated with static spacers. This study compares the clinical and radiographic two-year outcomes between patients treated with static or expandable interbody spacers with adjustable lordosis for Minimally Invasive Lateral Lumbar Interbody Fusion (MIS LLIF). Methods: This is a retrospective, multi-site, multi-surgeon, Institutional Review Board-exempt chart review of patients who underwent MIS LLIF using either a static (27 patients) or expandable spacer with adjustable lordosis (66 patients). Radiographs, complications and patient-reported outcomes were collected and compared from preoperative up to 24-month postoperative follow-up. Results: Mean improvement of Visual Analogue Scale back pain at 6, 12 and 24 months, as well as Oswestry Disability Index scores at 3, 6, 12, and 24 months, were significantly higher in the expandable group compared to the static group. The mean improvement of ODI scores from preoperative to 3, 6, 12, and 24 months was significantly greater in the expandable group by 55.6%, 75.6%, 77.4%, and 108.9% and by 48.2%, 34.6%, and 71.5% at 6, 12, and 24 months postoperatively for VAS pain scores, compared to the static group and (p<0.05) Disc height mean improvement from preoperative to 24 months was more significant in the static group compared to the expandable group. Implant subsidence was significantly greater in the static group (18.5%, 5/27 patients) compared to the expandable group (0/66 patients) (all p<0.05). Conclusion: This study showed significant positive clinical and radiographic outcomes for patients who underwent MIS LLIF using static or expandable interbody spacers with adjustable lordosis. Both static and expandable groups demonstrated long-term maintenance of significant radiographic improvements, with minimal complications reported and sustained significant clinical improvements at 24-month follow-up. There was a 0% subsidence rate in the expandable group, compared to an 18.5% subsidence rate in the static group. The use of expandable spacers with adjustable lordosis was safe and effective for the studied patient population.
可调节前凸膨胀性垫片:与传统的静态垫片在侧位腰椎椎体间融合中的比较?
导语:具有可调节前凸的可膨胀体间垫片设计用于原位膨胀,避免了诸如终板损伤、过度试验和与静态垫片相关的强力撞击等并发症。本研究比较了采用固定式或可伸缩式椎间间隔器进行微创侧位腰椎椎间融合术(MIS LLIF)的患者两年的临床和影像学结果。方法:这是一项回顾性的、多部位、多外科医生、机构审查委员会豁免的、使用静态(27例)或可调节前凸的可扩展间隔器(66例)接受MIS LLIF的患者的回顾性研究。收集术前至术后24个月随访期间的x线片、并发症和患者报告的结果进行比较。结果:与静态组相比,可扩展组在6、12和24个月时视觉模拟量表背部疼痛的平均改善,以及在3、6、12和24个月时的Oswestry残疾指数评分,显着高于静态组。术前至3、6、12、24个月ODI评分的平均改善,可扩组分别比静止组高55.6%、75.6%、77.4%、108.9%;术后6、12、24个月VAS疼痛评分的平均改善,分别比静止组高48.2%、34.6%、71.5% (p<0.05)。静态组(18.5%,5/27例)种植体下沉明显大于可扩展组(0/66例)(均p<0.05)。结论:该研究显示,使用静态或可伸缩前凸椎间间隔器接受MIS LLIF的患者具有显著的临床和影像学阳性结果。在24个月的随访中,静态组和可扩展组均表现出长期维持显著的放射学改善,并发症最少,并持续显著的临床改善。可膨胀组的沉降率为0%,而静态组的沉降率为18.5%。对于研究的患者群体来说,使用可调节前凸的可伸缩垫片是安全有效的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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