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Bridge-Enhanced ACL Repair: A Review of the Science and the Pathway through FDA Investigational Device Approval

机译:增强桥梁的ACL维修:审查科学和FDA批准研究器械的途径

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摘要

Injuries to the anterior cruciate ligament (ACL) are currently treated with replacement of the torn ligament with a graft of tendon harvested from elsewhere in the knee. This procedure, called "ACL reconstruction," is excellent for restoring gross stability to the knee; however, there are relatively high graft failure rates in adolescent patients,, , and the ACL reconstruction procedure does not prevent the premature osteoarthritis seen in patients after an ACL injury., , Thus, new solutions are needed for ACL injuries. Researchers have been investigating the use of scaffolds, growth factors and cells to supplement a suture repair of the ACL (bio-enhanced repair). In this paper, we will review the varied approaches, which have been investigated for stimulating ACL healing and repair in preclinical models and how one of these technologies was able to move from promising preclinical results to FDA acceptance of an Investigational Device Exemption (IDE) application for a first-in-human study.
机译:前交叉韧带(ACL)的损伤目前可通过用从膝盖其他地方收获的肌腱移植物代替撕裂的韧带来治疗。此过程称为“ ACL重建”,非常适合恢复膝盖的总体稳定性。然而,青少年患者的移植失败率较高,,并且ACL重建手术不能预防ACL损伤后的患者发生过早的骨关节炎。因此,需要针对ACL损伤的新解决方案。研究人员一直在研究使用支架,生长因子和细胞来补充ACL的缝合修复(生物增强修复)。在本文中,我们将回顾各种刺激临床前模型中ACL愈合和修复的方法,以及这些技术中的一种如何能够从有希望的临床前结果转变为FDA对研究器械豁免(IDE)应用的接受进行首次人类研究。

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