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[股骨内外侧假体十年经验评估——背景、数据与结果]

[Evaluation of 10 years experience with endo-exo femur prostheses - background, data and results].

作者信息

Aschoff H H, Juhnke D L

机构信息

Klinik f. Plastische, Hand- u. Rekonstruktive Chirurgie, Sana Kliniken Lübeck.

出版信息

Z Orthop Unfall. 2012 Dec;150(6):607-14. doi: 10.1055/s-0032-1327932. Epub 2012 Nov 21.

Abstract

Between 1999 and 2011 the Endo-Exo femur prosthesis has been applied to 54 patients. This comparatively new method for patient rehabilitation after upper leg amputation includes a two-step surgical procedure. The first step is an operation where the endomodule of the stem prosthesis is implanted in the bone via a press-fit technique. Then the soft tissue coat is closed to give the bone enough time for a secure osseointegration of the prosthesis. About six weeks later a stoma is cut out and the adapter for the exo-part is connected. The prosthesis is therefore intramedullary anchored and percutaneously penetrating the skin. A critical examination of this procedure has to put its main attention to the latent danger of an ascending, intramedullary infection. This may arise from the skin-penetrating stoma region at the distal stump. All data derived from patients operated in Lübeck, Germany have been evaluated focusing on reasons for objectionable operative procedures and their resulting terms of treatment. The evaluation shows that the initially high rate of stoma-associated infections of the soft tissue coat could be dramatically reduced through a change of design of the skin-penetrating parts. In between January 2009 and December 2011 (altogether 24 implants/23 patients) no operative revisions had to be undertaken because of infections of the stoma. Next to this there are more characteristics conditionally caused by the implant - like fractures of the affected extremity and other complications - presented in terms of cause-related case histories.

摘要

1999年至2011年间,Endo-Exo股骨假体应用于54例患者。这种用于大腿截肢后患者康复的相对较新的方法包括两步手术过程。第一步是通过压配技术将柄部假体的内模块植入骨内的手术。然后闭合软组织包膜,以便给骨足够的时间使假体实现牢固的骨整合。大约六周后,切开一个造口并连接外部分的适配器。因此,该假体是髓内固定并经皮穿透皮肤的。对该手术过程进行严格检查时,必须主要关注髓内感染上行的潜在风险。这可能源于远端残端的皮肤穿透造口区域。对在德国吕贝克接受手术的患者的所有数据进行了评估,重点关注不良手术操作的原因及其相应的治疗情况。评估表明,通过改变皮肤穿透部件的设计,软组织包膜最初与造口相关的感染率可大幅降低。在2009年1月至2011年12月期间(共24例植入/23例患者),没有因造口感染而进行手术翻修。除此之外,还根据与病因相关的病例记录介绍了更多由植入物引起的特征性情况,如患肢骨折和其他并发症。

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