Pain and Functional Outcomes Following Vertebroplasty for Vertebral Compression Fractures: A Tertiary Center Experience

Q Medicine
S. Mukherjee, J. Yeh, H. Ellamushi
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引用次数: 0

Abstract

Introduction:There is a dearth of comparative outcome data on vertebroplasty for the treatment of vertebral compression fractures (VCF) according to vertebral level, number of levels, and etiology. The aim of this study was to investigate improvement of pain and function following vertebroplasty for a heterogenous cohort of patients with medically refractory VCF. Materials and Methods:A prospective observational study was conducted on a cohort of consecutive patients undergoing vertebroplasty following at least 4 weeks of failed medical management, between April 2007 and March 2012 at a single Neurosurgical center. Pain Visual Analogue Scale (VAS) scores, Oswestry Disability Index (ODI) scores, analgesic usage, and complications were recorded preoperatively and at 1 day, 1 week, 1 month, 6 months, and 1 year postoperatively. Intraoperative vertebral body biopsy was performed routinely. Results:202 levels were augmented in 147 patients. The most common levels augmented were T12 (17%), L1 (18%), and L4 (10%). Significant reductions in pain VAS and ODI scores were evident at day 1 and sustained at up to 1 year postoperatively (P<0.001). They were not dependent on the level of fracture (T3-10, T11-L2, L3-S1) (P>0.05), number of levels treated (single level, 2 levels, >2 levels) (P>0.05), or etiology of VCF (P>0.05). At 1 year postoperatively, 79% (113/142) had no or reduced analgesic usage. The complication rate was 6% (9/147). There were 5 mortalities, none of which were directly related to surgery. Conclusions:Vertebroplasty for medically refractory VCF may offer sustained improvement in pain and function. The procedure is associated with low morbidity and mortality.
椎体压缩性骨折椎体成形术后的疼痛和功能结果:三级中心经验
根据椎体水平、水平数和病因,椎体成形术治疗椎体压缩性骨折(VCF)的比较结果数据缺乏。本研究的目的是调查一组难治性VCF患者椎体成形术后疼痛和功能的改善。材料和方法:在2007年4月至2012年3月间,在一个神经外科中心对连续接受椎体成形术的患者进行了一项前瞻性观察性研究,这些患者在至少4周的医疗管理失败后接受了椎体成形术。术前、术后1天、1周、1个月、6个月和1年分别记录疼痛视觉模拟评分(VAS)、Oswestry残疾指数(ODI)评分、镇痛药使用情况和并发症。术中常规进行椎体活检。结果:147例患者中202个水平升高。最常见的是T12(17%)、L1(18%)和L4(10%)。疼痛VAS和ODI评分在术后第1天明显降低,并持续到术后1年(P0.05),治疗水平(单水平,2水平,>水平)(P>0.05),或VCF病因(P>0.05)。术后1年,79%(113/142)患者没有或减少使用镇痛药。并发症发生率为6%(9/147)。有5例死亡,没有一例与手术直接相关。结论:椎体成形术治疗难治性VCF可持续改善疼痛和功能。该手术的发病率和死亡率较低。
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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来源期刊
Neurosurgery Quarterly
Neurosurgery Quarterly 医学-神经科学
CiteScore
0.08
自引率
0.00%
发文量
0
审稿时长
6-12 weeks
期刊介绍: Neurosurgery Quarterly synthesizes the broad wealth of material on international developments in the diagnosis, management, and surgical treatment of neurological disorders. By encompassing viewpoints from worldwide sources, the journal provides information in greater depth than is usually found in the medical literature.
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