谨慎乐观

Samuel A. Taylor
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This early enthusiasm has more recently been tempered by studies reporting significantly higher revision rates for ACL reconstructions performed with allograft compared with autograft tissue. The MOON group determined that use of allograft was a predictor of worse outcomes for the IKDC (International Knee Documentation Committee) questionnaire and KOOS (Knee injury and Osteoarthritis Outcome Score) and that the odds of revision were four times higher among those who underwent ACL reconstruction with allograft compared with autograft. A meta-analysis of 5182 patients reported a threefold increase in the rerupture rate for BTB (bone-patellar tendon-bone) allograft reconstruction (12.7%) compared with BTB autograft (4.4%). A Canadian study involving nearly 13,000 ACL reconstructions indicated that allograft use was an independent risk factor for revision within five years. Another study of 122 military cadets who had undergone ACL reconstruction prior to matriculation demonstrated that those who underwent allograft reconstruction were 7.7 times more likely to undergo subsequent revision. When reading the above studies, it is important to remember that these were often mixed cohorts with regard to graft fixation and, perhaps more importantly, allograft processing. The critical question remains: Is the problem the allograft tissue itself or the manner in which it is processed? Although this answer remains elusive, the authors of the present study have made a valiant effort to address this question. It would appear that processing does play a role in graft failure. For example, high-dose gamma irradiation has been demonstrated to have detrimental effects on the biomechanical properties of grafts. In response, some surgeons have traded the biomechanical risk for infection and immunologic risks—turning to fresh-frozen, nonirradiated, allograft tissue. 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Guo et al. identified three cases of acute synovitis that they believed were secondary to immunologic rejection among thirty-three patients who underwent fresh-frozen allograft ACL reconstruction. Is there a compromise that could reduce infection and immunogenicity while preserving mechanical properties? Perhaps e-beam irradiation is the solution. In fact, e-beam irradiation was shown previously to more closely preserve graft properties compared with gamma irradiation. The follow-up study, however, demonstrated adverse biomechanical effects of high-dose e-beam irradiation in an in vivo sheep ACL model. 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引用次数: 6

摘要

外科医生必须平衡新鲜冷冻同种异体移植组织的感染风险与终末辐照组织潜在的生物力学劣势。本研究的作者在确定不育性和稳定性之间的折衷方面取得了长足的进步。然而,我们建议读者,这些是来自实验室的生物力学结果,并不代表患者的结果。因此,在实施电子束(电子束)灭菌策略之前,应该研究体内动物模型的生物力学耐久性和组织学结合。ACL(前交叉韧带)重建涉及同种异体移植组织,在使用、接受和兴奋方面有明显的波动。最初,同种异体移植似乎是减少围手术期疼痛、限制发病率和加速恢复的答案。这种早期的热情最近因研究报道同种异体移植比自体移植组织进行ACL重建的翻修率明显更高而有所缓和。MOON小组确定,使用同种异体移植物是IKDC(国际膝关节文献委员会)问卷和oos(膝关节损伤和骨关节炎结局评分)结果较差的预测因素,并且与自体移植物相比,同种异体移植物进行ACL重建的患者翻修的几率高4倍。5182例患者的荟萃分析报告BTB(骨-髌腱-骨)异体移植重建的再破裂率(12.7%)比BTB自体移植(4.4%)增加了三倍。加拿大一项涉及近13000例ACL重建的研究表明,同种异体移植是5年内翻修的独立危险因素。另一项对122名在入学前接受过ACL重建的军校学员的研究表明,接受同种异体移植重建的学员接受后续翻修的可能性高出7.7倍。在阅读上述研究时,重要的是要记住,这些研究通常是关于移植物固定和更重要的同种异体移植物处理的混合队列。关键的问题仍然存在:问题是同种异体移植组织本身还是它的处理方式?虽然这个答案仍然难以捉摸,但本研究的作者已经做出了勇敢的努力来解决这个问题。看来,加工确实在移植物失败中起作用。例如,高剂量伽马辐射已被证明对移植物的生物力学特性有有害影响。因此,一些外科医生放弃了感染和免疫风险的生物力学风险,转而采用新鲜冷冻、未辐照的同种异体移植组织。最近的几项临床结果研究支持了这种外流。例如,一项系统综述显示自体移植物与非化学处理、非辐照的同种异体移植物之间没有差异。Mariscalco等人确定了9项前瞻性或回顾性比较研究,比较了自体移植物与未辐照的同种异体ACL重建,但未能确定移植物类型在失败、器械松弛或主观结果测量方面的任何显著差异。另一项针对年轻人群(小于25岁)的研究回顾性比较了53例自体BTB移植患者和28例未经处理的同种异体BTB移植重建患者,也没有发现上述结果测量的差异。Guo等人在33例接受新鲜冷冻同种异体ACL重建的患者中发现了3例急性滑膜炎,他们认为这是继发于免疫排斥反应。在保持机械性能的同时,是否存在一种可以减少感染和免疫原性的折衷方案?也许电子束照射是解决办法。事实上,与伽玛辐照相比,电子束辐照先前已被证明能更紧密地保持接枝性能。然而,后续研究表明,高剂量电子束辐照在羊ACL体内模型中具有不利的生物力学效应。其他研究人员发现,在实验室中,低剂量、中等剂量甚至高剂量的伽马辐射治疗的同种异体移植物与未处理的同种异体移植物具有相当的生物力学特性,但患者的临床结果不支持这种方法用于同种异体移植物灭菌。e142 (1)
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Cautious Optimism
Surgeons must balance the infection risk associated with fresh-frozen allograft tissue with the potential biomechanical inferiority of terminally irradiated tissue. The authors of the present study have made strides toward identifying a compromise between sterility and stability. We would suggest to the readers, however, that these are biomechanical results from the laboratory and do not represent patient outcomes. Thus, before the implementation of electron beam (e-beam) sterilization strategies, in vivo animal models should be investigated for biomechanical durability and histologic incorporation. ACL (anterior cruciate ligament) reconstruction involving allograft tissue has seen marked fluctuation with regard to use, acceptance, and excitement. Initially, allografts seemed to be the answer to reducing perioperative pain, limiting morbidity, and hastening recovery. This early enthusiasm has more recently been tempered by studies reporting significantly higher revision rates for ACL reconstructions performed with allograft compared with autograft tissue. The MOON group determined that use of allograft was a predictor of worse outcomes for the IKDC (International Knee Documentation Committee) questionnaire and KOOS (Knee injury and Osteoarthritis Outcome Score) and that the odds of revision were four times higher among those who underwent ACL reconstruction with allograft compared with autograft. A meta-analysis of 5182 patients reported a threefold increase in the rerupture rate for BTB (bone-patellar tendon-bone) allograft reconstruction (12.7%) compared with BTB autograft (4.4%). A Canadian study involving nearly 13,000 ACL reconstructions indicated that allograft use was an independent risk factor for revision within five years. Another study of 122 military cadets who had undergone ACL reconstruction prior to matriculation demonstrated that those who underwent allograft reconstruction were 7.7 times more likely to undergo subsequent revision. When reading the above studies, it is important to remember that these were often mixed cohorts with regard to graft fixation and, perhaps more importantly, allograft processing. The critical question remains: Is the problem the allograft tissue itself or the manner in which it is processed? Although this answer remains elusive, the authors of the present study have made a valiant effort to address this question. It would appear that processing does play a role in graft failure. For example, high-dose gamma irradiation has been demonstrated to have detrimental effects on the biomechanical properties of grafts. In response, some surgeons have traded the biomechanical risk for infection and immunologic risks—turning to fresh-frozen, nonirradiated, allograft tissue. This exodus is supported by several recent clinical outcomes studies. A systematic review, for example, revealed no difference between autograft and non-chemically processed, nonirradiated allograft. Mariscalco et al. identified nine prospective or retrospective comparative studies that compared autograft with nonirradiated allograft ACL reconstruction and failed to identify any significant differences between graft types with regard to failure, instrumented laxity, or subjective outcome measures. Another study of a younger population (less than twenty-five years old) retrospectively compared fifty-three patients who underwent BTB autograft with twenty-eight patients who underwent nonprocessed BTB allograft reconstruction and also found no difference with regard to the aforementioned outcome measures. Guo et al. identified three cases of acute synovitis that they believed were secondary to immunologic rejection among thirty-three patients who underwent fresh-frozen allograft ACL reconstruction. Is there a compromise that could reduce infection and immunogenicity while preserving mechanical properties? Perhaps e-beam irradiation is the solution. In fact, e-beam irradiation was shown previously to more closely preserve graft properties compared with gamma irradiation. The follow-up study, however, demonstrated adverse biomechanical effects of high-dose e-beam irradiation in an in vivo sheep ACL model. Other investigators found that allografts treated with low, moderate, and even high-dose gamma irradiation had comparable biomechanical properties to nonprocessed allograft in the laboratory, but the clinical outcomes in patients have not supported this method for allograft sterilization. e142(1)
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