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原发性髋关节置换假体及其证据基础:文献系统综述。

Primary hip replacement prostheses and their evidence base: systematic review of literature.

机构信息

University Hospitals Birmingham NHS Foundation Trust, The Old Queen Elizabeth Hospital, Edgbaston, Birmingham B15 2TH, UK.

出版信息

BMJ. 2013 Dec 19;347:f6956. doi: 10.1136/bmj.f6956.

Abstract

OBJECTIVE

To determine the extent to which prostheses with no readily available evidence to support their use are being implanted in primary total hip arthroplasty.

DESIGN

Systematic review of the literature.

DATA SOURCES

The 9th annual report of the National Joint Registry of England and Wales (NJR) was analysed to identify prostheses with an Orthopaedic Data Evaluation Panel rating of "unclassified" or "pre-entry" used in primary total hip arthroplasty in 2011. A systematic review of those prostheses was carried out using PubMed, Cochrane, Embase, OVID, and Google databases.

STUDY SELECTION

Prostheses used in primary total hip arthroplasty as published in the NJR's 9th annual report were analysed. Only literature that included the name of the prosthesis was included. Literature yielded in the search results was excluded if it reported animal, non-orthopaedic, non-total hip arthroplasty, or non-device related studies.

RESULTS

The systematic review found that 24% (57/235) of all hip replacement implants available to surgeons in the UK have no evidence for their clinical effectiveness. It also shows that 10,617 (7.8%) of the 136,593 components used in primary hip replacements in 2011 were implanted without readily identifiable evidence of clinical effectiveness. These comprised 157 cemented stems (0.5% of 34,655 implanted), 936 (2.8% of 33,367) uncemented stems, 1732 (7.1% of 24,349) cemented cups, and 7577 (17.1% of 44,222) uncemented cups.

CONCLUSIONS

This study shows that a considerable proportion of prostheses available to orthopaedic surgeons have no readily available evidence of clinical effectiveness to support their use. Concern exists about the current system of device regulation, and the need for a revised process for introducing new orthopaedic devices is highlighted.

摘要

目的

确定在初次全髋关节置换术中使用的假体中,有多少是没有现成证据支持其使用的。

设计

文献系统评价。

资料来源

对英格兰和威尔士国家关节登记处(NJR)的第 9 份年度报告进行了分析,以确定 2011 年在初次全髋关节置换术中使用的、具有矫形数据评估小组“未分类”或“预进入”评级的假体。使用 PubMed、Cochrane、Embase、OVID 和 Google 数据库对这些假体进行了系统评价。

研究选择

对 NJR 第 9 份年度报告中公布的初次全髋关节置换术中使用的假体进行了分析。仅包括文献中包含假体名称的文献。如果搜索结果中报告的是动物、非矫形、非全髋关节置换术或非器械相关的研究,则将其排除在外。

结果

系统评价发现,英国外科医生可使用的所有髋关节置换植入物中有 24%(57/235)没有临床有效性的证据。它还表明,2011 年初次髋关节置换术中使用的 136593 个部件中有 10617 个(7.8%)是在没有明确临床有效性证据的情况下植入的。这些包括 157 个骨水泥柄(34655 个植入物中的 0.5%)、936 个(33367 个中的 2.8%)非骨水泥柄、1732 个(24349 个中的 7.1%)骨水泥杯和 7577 个(44222 个中的 17.1%)非骨水泥杯。

结论

这项研究表明,相当一部分可供矫形外科医生使用的假体没有现成的临床有效性证据支持其使用。人们对当前的器械监管制度表示关注,并强调需要对引入新的矫形器械的过程进行修订。

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