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聚对苯二甲酸乙二酯膝关节韧带假体的界面与生物相容性。对用于前交叉韧带手术修复的失效合成植入物进行组织学和超微结构器械取出分析。

Interface and biocompatibility of polyethylene terephthalate knee ligament prostheses. A histological and ultrastructural device retrieval analysis in failed synthetic implants used for surgical repair of anterior cruciate ligaments.

作者信息

Kock H J, Stürmer K M, Letsch R, Schmit-Neuerburg K P

机构信息

Abteilung für Unfallchirurgie, Universitätsklinikum Gesamthochschule Essen, Germany.

出版信息

Arch Orthop Trauma Surg. 1994;114(1):1-7. doi: 10.1007/BF00454727.

Abstract

In a prospective clinical study of 54 patients with acute anterior cruciate ligament instability, 56 artificial ligaments made of polyethylene terephthalate (Trevira hochfest) were implanted to restore knee stability. The average follow-up of these artificial knee ligaments was 40.2 (12-79) months; five implants (10%) had to be explanted due to failure after an average of 17.8 (6-50) months. All explants were examined by histological and ultrastructural methods in a device retrieval analysis. With regard to short- and medium-term artificial ligament failure in the human knee joint, a non-isometric surgical implantation technique, inappropriate strain during rehabilitation and implant fatigue and wear were responsible for ligament failures.

摘要

在一项针对54例急性前交叉韧带不稳定患者的前瞻性临床研究中,植入了56条由聚对苯二甲酸乙二酯(特瑞维拉高强度)制成的人工韧带以恢复膝关节稳定性。这些人工膝关节韧带的平均随访时间为40.2(12 - 79)个月;5例植入物(10%)因失败在平均17.8(6 - 50)个月后不得不取出。在器械取出分析中,所有取出物均通过组织学和超微结构方法进行检查。关于人体膝关节人工韧带的短期和中期失败,非等距手术植入技术、康复期间不适当的应变以及植入物疲劳和磨损是韧带失败的原因。

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