Treatment of annular disc tears and “leaky disc syndrome” with fibrin sealant

Kevin Pauza MD , Carrie Wright BS , Adam Fairbourn BS
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引用次数: 1

Abstract

The surfaces of annulus fibrosus tears are known harbingers of inflammatory constituents within intervertebral discs, stimulating sensitized nocioceptors within those tears. Other current treatment options of internal disc disruption neglect to specifically address the surface of these tears. Therefore, this investigation answers the question: does nonautologous fibrin sealant applied to the surface of annulus fibrosus tears mechanically glue and seal annular tears? Regarding this query, results suggest nonautologous concentrated fibrin successfully seals annulus fibrosus tears with a “suture-like mechanical sealant,” serving as a safe option for treating symptomatic or nonsymptomatic intervertebral disc tears. Sealing tears prevents pain-generating chemicals of the nucleus pulposus from leaking through annular tears. More specifically, fibrin sealant minimizes or eliminates extravasation of nucleus pulposus through tears and voids within the annulus fibrosus. Moreover, an investigation subjecting discs to an “internal pressure challenge” objectively affirms fibrin׳s ability to seal torn and degenerated discs against a pressure challenge. (1 psi = 6.89476 kPs (disc mean pressure pretreatment = 75.84 kPs; post-treatment = 179.3 kPs: (n = 347, P < 0.001). Therefore, sealing annular tears serves to minimize extravasation of nucleus pulposus through annular tears, thus potentially treating symptoms caused by internal disc disruption, “Leaky Disc Syndrome,” and chemical radiculopathy. Additionally, sealing annular tears potentially allows adjunctive regenerative biologics such as mesenchymal precursor cells, platelet rich plasma, and growth factors to remain within discs, thus, potentially optimizing their efficacy. A prior in vivo investigation demonstrated the vast majority of mesenchymal stem cells leaked from animal intravertebral discs, and another demonstrated radiolabeled mesenchymal stem cells leaked from degenerated discs and were subsequently found within new exuberant osteophytes adjacent to the degenerated disc. Intra-annular nonautologous concentrated fibrin shares a benefit of other intradiscal biologics in that fibrin does not cause aberrant detrimental mechanical forces on adjacent discs, compared with surgical fusion and disc arthrodesis, which both cause aberrant, potentially damaging mechanical forces on adjacent segments. The mean number of morphologically abnormal lumbar intervertebral discs in this population with chronic low back pain was 3.21 discs.

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纤维蛋白密封剂治疗椎间盘环裂及“漏椎间盘综合征”
纤维环撕裂的表面是椎间盘炎症成分的已知先兆,刺激撕裂内敏感的伤害感受器。目前其他治疗内椎间盘破裂的选择忽视了具体解决这些撕裂的表面。因此,本研究回答了一个问题:应用于纤维环表面的非自体纤维蛋白密封剂是否会机械粘合并密封环撕裂?关于这个问题,结果表明非自体浓缩纤维蛋白成功地用“缝合线式机械密封剂”密封纤维环撕裂,作为治疗有症状或无症状椎间盘撕裂的安全选择。封闭裂口可以防止髓核中产生疼痛的化学物质通过环形裂口泄漏。更具体地说,纤维蛋白密封剂减少或消除髓核通过纤维环内的撕裂和空隙外渗。此外,一项对椎间盘进行“内部压力挑战”的调查客观地证实了纤维蛋白变化对压力挑战密封撕裂和退变椎间盘的能力。1 psi = 6.89476 kPs(阀瓣平均压力预处理= 75.84 kPs;后处理= 179.3 kPs:(n = 347, P <0.001)。因此,封闭环裂口有助于减少髓核通过环裂口外渗,从而有可能治疗由椎间盘破裂、“漏椎间盘综合征”和化学神经根病引起的症状。此外,封闭环状撕裂可能允许辅助再生生物制剂(如间充质前体细胞、富血小板血浆和生长因子)留在椎间盘内,从而潜在地优化其疗效。先前的一项体内研究表明,绝大多数间充质干细胞从动物椎间盘中渗出,另一项研究表明,放射性标记的间充质干细胞从退变椎间盘中渗出,随后在退变椎间盘附近的新生旺盛的骨赘中发现。与手术融合术和椎间盘融合术相比,环内非自体浓缩纤维蛋白与其他椎间盘内生物制剂有相同的优点,即纤维蛋白不会对相邻椎间盘造成异常的有害机械力,而手术融合术和椎间盘融合术会对相邻节段造成异常的、潜在的破坏性机械力。在这群慢性腰痛患者中,形态异常的腰椎间盘平均数目为3.21个。
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