Orthopaedics Department, Radboud Institute for Health Sciences, Radboud University Medical Center, Nijmegen, The Netherlands.
Centre of Precision Rehabilitation for Spinal Pain, School of Sport, Exercise and Rehabilitation Sciences, College of Life and Environmental Sciences, University of Birmingham, Birmingham, UK.
Eur Spine J. 2019 Apr;28(4):696-709. doi: 10.1007/s00586-018-5680-3. Epub 2018 Jul 11.
Lumbar spinal fusion (LSF) is frequently and increasingly used in lumbar degenerative disorders despite conflicting results and recommendations. A thorough understanding of patient outcomes after LSF is required to inform decisions regarding surgery and to improve post-surgery management. The current study aims to evaluate the course of pain and disability in patients with degenerative disorders of the lumbar spine after first-time LSF.
A systematic review and meta-analysis of pain and disability outcomes in prospective cohort studies up to 31 March 2017 is identified in four electronic databases. Two independent researchers determined study eligibility, extracted data, and assessed risk of bias (modified Quality in Prognostics tool). A random effects model (maximum likelihood) was used to calculate means and 95% confidence intervals. The primary analysis was performed on complete data, and a sensitivity analysis was performed on all data.
Twenty-five studies (n = 1777 participants) were included. The mean (95% confidence interval) Visual Analogue Scale (VAS) back pain (n = 9 studies) decreased from 64 (57-71) pre-surgery to 20 (16-24) at 24-month follow-up. Leg pain (n = 9 studies) improved from VAS 70 (65-74) pre-surgery to 17 (12-23) at 24-month interval. Disability (n = 12 studies), measured with the Oswestry Disability Index, decreased from 44.8 (40.1-49.4) pre-surgery to 17.3 (11.9-22.8) at 24-month follow-up. The sensitivity analysis yielded similar results.
There is a substantial improvement in pain and disability after first-time LSF for degenerative disorders. However, long-term outcomes indicate that leg pain might be more reduced and for a longer period of time than axial back pain and disability. Registration PROSPERO CRD42015026922. These slides can be retrieved under Electronic Supplementary Material.
尽管存在相互矛盾的结果和建议,但腰椎融合术(LSF)在腰椎退行性疾病中的应用仍越来越频繁。为了为手术决策提供信息并改善术后管理,需要全面了解 LSF 后患者的结局。本研究旨在评估首次 LSF 后退行性腰椎疾病患者的疼痛和残疾进展情况。
通过在四个电子数据库中进行系统检索和荟萃分析,确定了截至 2017 年 3 月 31 日的前瞻性队列研究中关于疼痛和残疾结局的资料。两位独立的研究者确定了研究的纳入标准,提取了数据,并评估了偏倚风险(改良预后质量工具)。采用随机效应模型(最大似然法)计算平均值和 95%置信区间。主要分析基于完整数据进行,敏感性分析基于所有数据进行。
共纳入 25 项研究(n=1777 名参与者)。24 个月随访时,视觉模拟评分(VAS)腰痛(n=9 项研究)从术前的 64(57-71)降至 20(16-24)。腿痛(n=9 项研究)从术前 VAS70(65-74)改善至 24 个月随访时的 17(12-23)。使用 Oswestry 残疾指数(ODI)测量的残疾程度(n=12 项研究)从术前的 44.8(40.1-49.4)降至 24 个月随访时的 17.3(11.9-22.8)。敏感性分析得出了相似的结果。
退行性疾病首次行 LSF 后,疼痛和残疾有明显改善。然而,长期结果表明,腿痛缓解的程度和持续时间可能优于轴向腰痛和残疾。登记号:PROSPERO CRD42015026922。这些幻灯片可在电子补充材料中获取。