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Reducing Lumbar Discogenic Back Pain and Disability with Intradiscal Injection of Bone Marrow Concentrate: 5-year Follow-up 椎间盘内注射骨髓浓缩液减轻腰椎间盘源性背痛和残疾:5年随访
Pub Date : 2018-10-01 DOI: 10.5923/J.AJSCR.20180201.01
Kenneth Pettine M. D., M. Dordevic, Michael Hasz M. D.
Background Context: Surgical treatments of discogenic lumbar back pain are fusion or lumbar artificial disc replacement. Studies comparing lumbar fusion with nonsurgical treatment found no difference in clinical results. Studies comparing lumbar fusion with lumbar artificial disc replacement have had mixed results. In a study with 12-month follow-up, our colleagues reported that intradiscal injections of autologous bone marrow concentrated cells resulted in substantial reductions in pain and disability without treatment complications or other adverse events. Purpose: This article reports a 5-year follow-up of treating lumbar discogenic back pain and disability with bone marrow concentrate. Study Design/Setting: Prospective, open-label, single-center case series. Patient Sample: The initial 26 participants were all surgical candidates according to their history of low back pain, nonsurgical treatment, and measurements of pain, disability, and disc degeneration. Outcome Measures: Visual Analog Scale of pain, and Oswestry Disability Index. Methods: Study design and clinical protocol, bone marrow collection and processing, and intradiscal injection were as previously described in the initial report. The study did not receive any outside funding. The disposable aspiration kits for the BMC injections, which cost about $20 each, were provided without charge by Celling Biosciences, Austin, Texas. Results: Of the initial 26 participants, six proceeded to surgery within 3 years of follow up. Of the remaining 20, 19 were available for follow-up at 5 years. Absolute and percentage reductions in pain and disability scores were sustained through the 5-year follow-up. No adverse events were reported through the 5 years. Conclusions: It may be reasonable to consider injecting participants who have discogenic back pain at one or two levels with bone marrow concentrate before they proceed to surgery.
背景:椎间盘源性腰背痛的手术治疗是融合术或人工腰椎间盘置换术。比较腰椎融合术与非手术治疗的研究发现临床结果没有差异。比较腰椎融合术与腰椎人工椎间盘置换术的研究结果好坏参半。在一项为期12个月的随访研究中,我们的同事报告了椎间盘内注射自体骨髓浓缩细胞可显著减少疼痛和残疾,且无治疗并发症或其他不良事件。目的:本文报道了用骨髓浓缩液治疗腰椎间盘源性背痛和残疾的5年随访。研究设计/设置:前瞻性、开放标签、单中心病例系列。患者样本:最初的26名参与者根据他们的腰痛史、非手术治疗、疼痛、残疾和椎间盘退变的测量都是手术候选人。结果测量:视觉模拟疼痛量表和Oswestry残疾指数。方法:研究设计和临床方案,骨髓收集和处理,以及椎间盘内注射如先前在初始报告中所述。这项研究没有获得任何外部资助。BMC注射剂的一次性吸吸包每个售价约20美元,由德克萨斯州奥斯汀的塞林生物科学公司免费提供。结果:在最初的26名参与者中,有6人在3年的随访中进行了手术。在剩下的20人中,有19人可以在5年后进行随访。在5年的随访中,疼痛和残疾评分的绝对和百分比都持续下降。5年无不良事件报告。结论:对于有椎间盘源性背痛的患者,在进行手术前,考虑给他们注射骨髓浓缩物可能是合理的。
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引用次数: 8
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American Journal of Stem Cell Research
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