使用 Tritanium C 前路颈椎固定架与 PEEK 固定架进行前路颈椎椎间盘切除术和融合术的临床疗效对比。

IF 1.2 Q3 SURGERY Spine Surgery and Related Research Pub Date : 2024-02-14 eCollection Date: 2024-07-27 DOI:10.22603/ssrr.2023-0140
Andrew J Croft, Abigail J Wiedel, Anthony M Steinle, Omar Zakieh, Jacquelyn S Pennings, Claudia Davidson, Scott L Zuckerman, Amir M Abtahi, Byron F Stephens
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引用次数: 0

摘要

导言:前路颈椎椎间盘切除融合术(ACDF)已被证明是治疗颈椎退行性病变患者的一种临床有效且经济有效的方法。目前正在开发新的椎间植入产品,以改善融合和稳定性,同时减少并发症。本研究评估了 Tritanium C(Tri-C)前路颈椎笼(史赛克)与聚醚醚酮(PEEK)颈椎笼相比在治疗颈椎椎间盘退行性病变(DDD)方面的有效性:利用从两家机构收集的前瞻性数据进行了回顾性队列分析。方法:利用从两家机构收集的前瞻性数据进行了回顾性队列分析,确定了使用 Tri-C 骨架或 PEEK 骨架接受 ACDF 治疗 DDD 的患者。收集了患者的人口统计学特征、合并症、手术变量和基线患者报告结果(PROs)。患者报告结果包括颈部残疾指数(NDI)以及颈部和手臂疼痛的数字评分量表(NRS)。主要结果包括 3 个月和 12 个月的患者报告结果以及 90 天再入院率、90 天再次手术率和围术期并发症率。放射学结果包括12个月内的下沉率、骨笼移动率和成功融合率。多变量线性回归模型用于确定预测12个月PROs的变量:本研究共纳入了 275 名接受 ACDF 的患者,并将其分为两组:PEEK组(213人)和Tri-C组(62人)。两组患者的颈部和手臂疼痛以及术后 NDI 均有所改善。对 Tri-C 和 PEEK 进行比较后发现,颈部或手臂疼痛或 NDI 在 3 个月或 12 个月后的变化无明显差异。此外,90 天再入院率、90 天再次手术率和围术期并发症率也没有差异。回归分析显示,Tri-C与PEEK对任何结果都没有显著的预测作用:结论:我们的研究结果表明,在 ACDFs 中使用多孔钛 Tri-C 骨架是治疗颈椎 DDD 的一种有效方法,它可以改善患者的 PROs、围手术期发病率和放射学参数。使用Tri-C保持架进行ACDF手术的患者与使用PEEK保持架的患者在临床结果上没有明显差异:证据等级:III。
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Clinical Effectiveness of Anterior Cervical Discectomy and Fusion Using Tritanium C Anterior Cervical Cage vs. PEEK Cage.

Introduction: Anterior cervical discectomy and fusion (ACDF) has proven to be a clinically efficient and cost-effective method for treating patients with degenerative cervical spine conditions. New intervertebral implant products are being developed to improve fusion and stability while decreasing complications. This study assesses the effectiveness of Tritanium C (Tri-C) Anterior Cervical Cage (Stryker) in the treatment of degenerative disk disease (DDD) of the cervical spine compared with polyetheretherketone (PEEK) cages.

Methods: A retrospective cohort analysis was conducted using data prospectively collected from two institutions. Patients who underwent ACDFs for DDD using either the Tri-C cage or PEEK cage were identified. The patients' demographics, comorbidities, operative variables, and baseline patient-reported outcomes (PROs) were collected. PROs included the Neck Disability Index (NDI) and numeric rating scale (NRS) for neck and arm pain. The primary outcomes included 3- and 12-month PROs as well as the rates of 90-day readmission, 90-day reoperation, and perioperative complication. The radiographic outcomes included rates of subsidence, cage movement, and successful fusion within 12 months. Multivariate linear regression models were run to identify variables predictive of 12-month PROs.

Results: A total of 275 patients who underwent ACDF were included in this study and were divided into two groups: PEEK (n=213) and Tri-C (n=62). Both groups showed improvement in neck and arm pain and NDI postoperatively. When Tri-C and PEEK were compared, no significant differences were observed in the 3- or 12-month changes in neck or arm pain or NDI. Furthermore, there were no differences in the rates of 90-day readmission, 90-day reoperation, and perioperative complication. Regression analysis revealed that Tri-C vs. PEEK was not a significant predictor of any outcome.

Conclusions: Our results indicate that the use of porous titanium Tri-C cage during ACDFs is an effective method for managing cervical DDD in terms of PROs, perioperative morbidity, and radiologic parameters. No significant difference was observed in any clinical outcome between patients undergoing ACDF using the Tri-C cage and those in whom the PEEK cage was used.

Level of evidence: III.

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