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完全浸渍羟基磷灰石聚醚醚酮椎间融合器在前路颈椎手术中融合的有效性

Effectiveness of a Fully Impregnated Hydroxyapatite Polyetheretherketone Cage on Fusion in Anterior Cervical Spine Surgery.

作者信息

Chin Kingsley R, Gohel Nishant N, Aloise Daniel M, Seale Jason A, Pandey Deepak K, Pencle Fabio J

机构信息

Orthopedics, Florida International University, Miami, USA.

Orthopedics, Less Exposure Surgery (LES) Clinic, Hollywood, USA.

出版信息

Cureus. 2021 Aug 26;13(8):e17457. doi: 10.7759/cureus.17457. eCollection 2021 Aug.

Abstract

Introduction Anterior cervical discectomy and fusion (ACDF) is the gold standard for the treatment of cervical spondylosis. However, new techniques, technologies, and improved implants have aided surgeons in reducing operative time with enhanced patient outcomes. Impregnated hydroxyapatite polyetheretherketone (HA PEEK) cages (Arena-C HA®, LESspine Inc. Malden, MA) are one such option that has aimed to increase the fusion rate. The authors herein aimed to assess the use of HA PEEK interbody cages by looking at outcomes, complications, and radiographic fusion.  Methods The medical records of 41 consecutive patients undergoing single-level ACDF with impregnated HA PEEK cages (group 1) were compared to the control group of 47 patients who had single-level ACDF without impregnated HA PEEK cages (group 2). Outcomes assessed included Visual Analog Scale (VAS) neck, Neck Disability Index (NDI) scores, radiographic fusion, and complication rates.  Results Of the 41 patients in group 1 (HA PEEK), 48% were female population with a mean age of 58.5+/- 1.7 years and BMI 29.7+/-1.2 kg/m. Of the 47 patients in group 2 (non-HA PEEK), 53% were female with a mean age of 54.3+/- 1.2 years and BMI 27.8+/-0.8 kg/m. Using t-test, there was a statistically significant intergroup difference in two-year VAS neck and NDI scores, p=0.007, and p=0.001, respectively. Radiographic fusion occurred as early as three months in the HA PEEK group.  Conclusions This study has demonstrated the equivalence of impregnated HA PEEK cages in single-level ACDF. Significant improvements were seen in VAS and NDI scores in the HA PEEK group. There was no incidence of heterotopic bone formation or reaction to HA PEEK cages. Additionally, a trend toward fusion was seen in HA PEEK patients as early as three to five months compared to seven to eight months for the ACDF group. We conclude that HA PEEK cages can be safely placed with excellent outcomes. However, further studies are required to look at added benefits.

摘要

引言 颈椎前路椎间盘切除融合术(ACDF)是治疗颈椎病的金标准。然而,新技术、新工艺以及改良的植入物有助于外科医生缩短手术时间并改善患者预后。含浸羟基磷灰石聚醚醚酮(HA PEEK)椎间融合器(Arena-C HA®,LESspine公司,马尔登,马萨诸塞州)就是旨在提高融合率的一种选择。本文作者旨在通过观察疗效、并发症及影像学融合情况来评估HA PEEK椎间融合器的使用效果。

方法 将41例连续接受单节段ACDF并使用含浸HA PEEK椎间融合器的患者(第1组)的病历与47例接受单节段ACDF但未使用含浸HA PEEK椎间融合器的患者(第2组)的病历进行比较。评估的疗效指标包括视觉模拟量表(VAS)颈部评分、颈部功能障碍指数(NDI)评分、影像学融合情况及并发症发生率。

结果 在第1组(HA PEEK)的41例患者中,48%为女性,平均年龄58.5±1.7岁,体重指数29.7±1.2kg/m²。在第2组(非HA PEEK)的47例患者中,53%为女性,平均年龄54.3±1.2岁,体重指数27.8±0.8kg/m²。使用t检验,两组在术后两年的VAS颈部评分和NDI评分上存在统计学显著差异,p值分别为0.007和0.001。HA PEEK组最早在术后三个月出现影像学融合。

结论 本研究证明了含浸HA PEEK椎间融合器在单节段ACDF中的等效性。HA PEEK组的VAS和NDI评分有显著改善。未发生异位骨形成或对HA PEEK椎间融合器的反应。此外,与ACDF组术后七至八个月相比,HA PEEK组患者在术后三至五个月就出现了融合趋势。我们得出结论,HA PEEK椎间融合器可以安全植入并取得良好疗效。然而,需要进一步研究以探讨其更多益处。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fc9b/8475745/2ab03dd37ce1/cureus-0013-00000017457-i04.jpg

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