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在非设计中心使用埃克塞特V40骨水泥型股骨柄至少十年的结果。

Outcomes of the Exeter V40 cemented femoral stem at a minimum of ten years in a non-designer centre.

作者信息

Mahon John, McCarthy Cathal Jack, Sheridan Gerard A, Cashman James P, O'Byrne John M, Kenny Paddy

机构信息

Cappagh National Orthopaedic Hospital, Dublin, Ireland.

Connolly Hospital Blanchardstown, Dublin, Ireland.

出版信息

Bone Jt Open. 2020 Dec 7;1(12):743-748. doi: 10.1302/2633-1462.112.BJO-2020-0163.R1.

Abstract

AIMS

The Exeter V40 cemented femoral stem was first introduced in 2000. The largest single-centre analysis of this implant to date was published in 2018 by Westerman et al. Excellent results were reported at a minimum of ten years for the first 540 cases performed at the designer centre in the Exeter NHS Trust, with stem survivorship of 96.8%. The aim of this current study is to report long-term outcomes and survivorship for the Exeter V40 stem in a non-designer centre.

METHODS

All patients undergoing primary total hip arthroplasty using the Exeter V40 femoral stem between 1 January 2005 and 31 January 2010 were eligible for inclusion. Data were collected prospectively, with routine follow-up at six to 12 months, two years, five years, and ten years. Functional outcomes were assessed using Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC) scores. Outcome measures included data on all components in situ beyond ten years, death occurring within ten years with components in situ, and all-cause revision surgery.

RESULTS

A total of 829 stems in 745 patients were included in the dataset; 155 patients (20.8%) died within ten years, and of the remaining 664 stems, 648 stems (97.6%) remained in situ beyond ten years. For the 21 patients (2.5%) undergoing revision surgery, 16 femoral stems (1.9%) were revised and 18 acetabular components (2.2%) were revised. Indications for revision in order of decreasing frequency were infection (n = 6), pain (n = 6), aseptic component loosening (n = 3), periprosthetic fracture (n = 3), recurrent dislocation (n = 2), and noise production (ceramic-on-ceramic squeak) (n = 1). One patient was revised for aseptic stem loosening. The mean preoperative WOMAC score was 61 (SD 15.9) with a mean postoperative score of 20.4 (SD 19.3) (n = 732; 88.3%).

CONCLUSION

The Exeter V40 cemented femoral stem demonstrates excellent functional outcomes and survival when used in a high volume non-designer centre. Outcomes are comparable to those of its serially validated predecessor, the Exeter Universal stem.Cite this article: 2020;1-12:743-748.

摘要

目的

埃克塞特V40骨水泥型股骨柄于2000年首次推出。迄今为止,对该植入物最大规模的单中心分析由韦斯特曼等人于2018年发表。报告显示,在埃克塞特国民保健服务信托基金的设计中心进行的前540例手术中,至少随访十年的结果优异,股骨柄生存率为96.8%。本研究的目的是报告在非设计中心使用埃克塞特V40股骨柄的长期结果和生存率。

方法

所有在2005年1月1日至2010年1月31日期间使用埃克塞特V40股骨柄进行初次全髋关节置换术的患者均符合纳入标准。前瞻性收集数据,常规随访时间为6至12个月、2年、5年和10年。使用西安大略和麦克马斯特大学骨关节炎指数(WOMAC)评分评估功能结果。结果指标包括超过十年仍在位的所有组件的数据、组件在位时十年内发生的死亡以及全因翻修手术。

结果

数据集中共纳入了745例患者的829个股骨柄;155例患者(20.8%)在十年内死亡,在其余664个股骨柄中,648个股骨柄(97.6%)超过十年仍在位。在接受翻修手术的21例患者(2.5%)中,16个股骨柄(1.9%)进行了翻修,18个髋臼组件(2.2%)进行了翻修。翻修指征按频率递减顺序为感染(n = 6)、疼痛(n = 6)、无菌性组件松动(n = 3)、假体周围骨折(n = 3)、复发性脱位(n = 2)和产生噪音(陶瓷对陶瓷摩擦声)(n = 1)。1例患者因无菌性股骨柄松动进行了翻修。术前WOMAC评分平均为61(标准差15.9),术后平均评分为20.4(标准差19.3)(n = 732;88.3%)。

结论

埃克塞特V40骨水泥型股骨柄在高容量非设计中心使用时显示出优异的功能结果和生存率。结果与其经过系列验证的前身埃克塞特通用股骨柄相当。引用本文:2020;1 - 12:743 - 748。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/191c/7750737/e1783c69e6cf/BJO-1-743-g0001.jpg

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