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["植入物的“混合”,一个基本问题"]

["Mixing" of implants, a basic problem].

作者信息

Baumgart F

机构信息

AO-Stiftung, Produkteinformation, Davos.

出版信息

Helv Chir Acta. 1990 Nov;57(3):495-513.

PMID:2269639
Abstract

The so-called "mixing" of implants and instruments of different producers in hospitals leads to some risks. The use of standardized implant materials (e.g. stainless steel ISO 5832/1) by different producers is necessary but not sufficient for combining an osteosynthesis plate and a bone screw from different sources. The design, the dimensions and tolerances, the manufacturing, the quality control, the well tested applicational technique can be different too for the implants and the necessary instruments as well. This may lead to damage, failure or fracture of the biomechanical system called "osteosynthesis", that means failure of the therapy. Finally the patient pays for the problems. Some examples illustrate the potential problems for the involved staff or institutions. The use of a unique consistent well tested and approved set of implants and instruments must be recommended strongly to avoid any additional risk.

摘要

医院中不同生产商的植入物和器械的所谓“混用”会带来一些风险。不同生产商使用标准化的植入材料(如不锈钢ISO 5832/1)对于组合不同来源的接骨板和骨螺钉来说是必要的,但并不充分。植入物和所需器械的设计、尺寸和公差、制造、质量控制以及经过充分测试的应用技术也可能不同。这可能导致被称为“骨接合术”的生物力学系统受损、故障或断裂,即治疗失败。最终,患者要为这些问题买单。一些例子说明了相关工作人员或机构可能面临的潜在问题。必须强烈推荐使用一套经过充分测试和批准的、独特且一致的植入物和器械,以避免任何额外风险。

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