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挪威联合登记处。

The Norwegian Joint Registry.

作者信息

Havelin L I

机构信息

Department of Orthopaedic Surgery at Haukeland University Hospital, Bergen, Norway.

出版信息

Bull Hosp Jt Dis. 1999;58(3):139-47.

Abstract

The Norwegian Orthopaedic Association established The Norwegian Arthroplasty Register in 1987, first as a hip prosthesis register, but from January 1994 it was extended to include all artificial joints. The main aim has been to survey the results of joint replacement surgery. The orthopaedic surgeons in all hospitals in the country of Norway have agreed to participate. More than 60,000 total hip replacements have been registered so far. Both primary operations and revisions are reported, and by using the patients' national identification numbers, we can link the revisions to the primary operation and perform survival analysis of the implants, with adjustment for potential confounding by factors such as age, gender, and diagnosis. As the prosthesis components are registered on an individual basis, survival of components such as the cup or the stem can be calculated separately, with revision used as an end-point. The reason for revision is registered, and we can assess the rate of revision due to aseptic loosening of the stem or cup, infection, dislocation, wear, osteolysis, or other reasons. For the safety of the surgeons, and to obtain a complete reporting of failures, we do not register the name of the surgeons and we keep the individual hospitals' results confidential. The operating costs of register are covered by the state and the register is not dependent on grants from the industry. The cost per registered implant is approximately $18 (US). With this system we have been able to detect inferior results of implants as early as after three years of use. Several brands of uncemented prostheses and two brands of cement have been withdrawn from the market mainly based on our findings.

摘要

挪威骨科协会于1987年设立了挪威关节置换登记处,最初是作为髋关节假体登记处,但从1994年1月起扩展到包括所有人工关节。主要目的是调查关节置换手术的结果。挪威全国所有医院的骨科医生都同意参与。到目前为止,已经登记了超过60,000例全髋关节置换手术。初级手术和翻修手术都有报告,通过使用患者的国家身份证号码,我们可以将翻修手术与初级手术联系起来,并对植入物进行生存分析,同时对年龄、性别和诊断等潜在混杂因素进行调整。由于假体组件是逐个登记的,髋臼或股骨柄等组件的生存率可以单独计算,以翻修作为终点。翻修原因会被登记,我们可以评估由于股骨柄或髋臼无菌性松动、感染、脱位、磨损、骨溶解或其他原因导致的翻修率。为了外科医生的安全,并获得完整的失败报告,我们不登记外科医生的姓名,并对各个医院的结果保密。登记处的运营成本由国家承担,登记处不依赖行业拨款。每个登记植入物的成本约为18美元(美国)。通过这个系统,我们能够早在使用三年后就检测到植入物的不良结果。几个品牌的非骨水泥假体和两个品牌的骨水泥已主要根据我们的调查结果退出市场。

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