Short-term clinical outcomes and safety of the SpineJack implant system for the treatment of pathological vertebral compression fractures in cancer patients: A retrospective analysis.

IF 2.5 3区 医学 Q2 ANESTHESIOLOGY
Pain Practice Pub Date : 2025-03-01 DOI:10.1111/papr.70020
Jason Parmar, Aila Malik, Gelilla Zemmedhun, Saba Javed
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引用次数: 0

Abstract

Background: The SpineJack implant system is an FDA-approved treatment modality for vertebral compression fractures (VCFs) with reported clinical efficacy comparable to the gold-standard balloon kyphoplasty. Specifically, there is insufficient literature regarding the treatment and safety outcomes of the SpineJack when analyzing a specific subset of patients such as the cancer population.

Methods: This is an institutional-level retrospective study at a cancer center on the SpineJack implant consisting of 67 cancer patients (mean age 64 ± 13 years) undergoing a total of 94 SpineJack implantations inserted at 15 thoracolumbar vertebral levels for the treatment of pathologic vertebral compression fractures. The primary outcome of the study was the change in pain score based on the Numeric Rating Scale (NRS) and the secondary outcome was the change in opioid requirement based on morphine milligram equivalents (MME). The average follow-up period was 2 weeks.

Results: Post-procedure, a statistically significant decrease in pain severity was observed, with the mean pain score improving from 7.72 ± 2.29 points to 3.45 ± 2.55 points (p-value < 0.0001). Additionally, a reduction in opioid requirement was noted, with a decrease in MME from 66.42 ± 92.66 mg preoperatively to 43.1 ± 60.78 mg (p-value < 0.0001) postoperatively. There was a 1.5% (N = 1) incidence of adjacent level fracture (ALF) reported over an average of 2-week follow-up. The most common intraoperative complication reported was cement extravasation.

Conclusion: Overall, treatment of cancer patients with pathologic fractures using the SpineJack procedure resulted in remarkably decreased pain scores, overall decreased MME requirements, a significantly low incidence of ALF (s), and minor intraoperative complications without long-term consequences. The SpineJack procedure is a clinically effective, low-risk treatment option for cancer patients with symptomatic, pathologic VCFs.

背景:SpineJack 植入系统是美国食品及药物管理局(FDA)批准的一种治疗椎体压缩性骨折(VCF)的方法,据报道其临床疗效与黄金标准的球囊椎体后凸成形术相当。具体而言,在分析特定患者群体(如癌症患者)时,有关 SpineJack 的治疗和安全性结果的文献不足:这是一项在癌症中心进行的关于 SpineJack 植入物的机构级回顾性研究,共有 67 名癌症患者(平均年龄为 64 ± 13 岁)接受了共 94 次 SpineJack 植入术,植入的椎体位于 15 个胸腰椎水平,用于治疗病理性椎体压缩骨折。研究的主要结果是基于数字评分量表(NRS)的疼痛评分变化,次要结果是基于吗啡毫克当量(MME)的阿片类药物需求变化。平均随访时间为 2 周:结果:手术后,疼痛严重程度出现了统计学意义上的显著下降,平均疼痛评分从 7.72 ± 2.29 分降至 3.45 ± 2.55 分(P 值 结论:手术后,疼痛严重程度出现了统计学意义上的显著下降,平均疼痛评分从 7.72 ± 2.29 分降至 3.45 ± 2.55 分(P 值 结论):总体而言,使用 SpineJack 手术治疗病理性骨折的癌症患者,疼痛评分明显降低,所需 MME 总体减少,ALF(s)发生率明显降低,术中并发症较少,且无长期后果。对于有症状的病理性 VCF 癌症患者来说,SpineJack 手术是一种临床有效、低风险的治疗方案。
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来源期刊
Pain Practice
Pain Practice ANESTHESIOLOGY-CLINICAL NEUROLOGY
CiteScore
5.60
自引率
3.80%
发文量
92
审稿时长
6-12 weeks
期刊介绍: Pain Practice, the official journal of the World Institute of Pain, publishes international multidisciplinary articles on pain and analgesia that provide its readership with up-to-date research, evaluation methods, and techniques for pain management. Special sections including the Consultant’s Corner, Images in Pain Practice, Case Studies from Mayo, Tutorials, and the Evidence-Based Medicine combine to give pain researchers, pain clinicians and pain fellows in training a systematic approach to continuing education in pain medicine. Prior to publication, all articles and reviews undergo peer review by at least two experts in the field.
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