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髋关节和膝关节置换植入物通用仿制品的制造:它受到监管吗?能省钱吗?

The manufacture of generic replicas of implants for arthroplasty of the hip and knee: is it regulated and will it save money?

作者信息

Atrey A, Heylen S, Gosling O, Porteous M J L, Haddad F S

机构信息

West Suffolk Hospital, Hardwick Ln, Bury St Edmunds, Suffolk, IP33 2QZ, UK.

University Hospital Antwerp, Antwesp, Belgium.

出版信息

Bone Joint J. 2016 Jul;98-B(7):892-900. doi: 10.1302/0301-620X.98B7.37016.

Abstract

Joint replacement of the hip and knee remain very satisfactory operations. They are, however, expensive. The actual manufacturing of the implant represents only 30% of the final cost, while sales and marketing represent 40%. Recently, the patents on many well established and successful implants have expired. Companies have started producing and distributing implants that purport to replicate existing implants with good long-term results. The aims of this paper are to assess the legality, the monitoring and cost saving implications of such generic implants. We also assess how this might affect the traditional orthopaedic implant companies. Cite this article: Bone Joint J 2016;98-B:892-900.

摘要

髋关节和膝关节置换术仍然是非常令人满意的手术。然而,它们成本高昂。植入物的实际制造成本仅占最终成本的30%,而销售和营销成本占40%。最近,许多成熟且成功的植入物专利已经到期。一些公司开始生产和销售声称能复制现有植入物且长期效果良好的植入物。本文旨在评估此类通用植入物的合法性、监测情况以及成本节约的影响。我们还评估了这可能如何影响传统的骨科植入物公司。引用本文:《骨与关节杂志》2016年;98 - B:892 - 900。

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