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用于治疗关节炎的全肩关节置换术中关节盂组件的长期存活情况。

Long-term survival of the glenoid components in total shoulder replacement for arthritis.

作者信息

Gazielly Dominique F, Scarlat Marius M, Verborgt Olivier

机构信息

The Shoulder Unit, Clinique Genollier, Genollier, Switzerland.

出版信息

Int Orthop. 2015 Feb;39(2):285-9. doi: 10.1007/s00264-014-2637-y. Epub 2014 Dec 24.

Abstract

PURPOSE

Aseptic glenoid component loosening remains a common problem in total shoulder arthroplasty (TSA). This study presents long-term prospective follow-up after implantation of a glenoid component using the "cancellous compaction technique" and its effect on clinical outcome and presence and progression of radiolucent lines (RLLs).

METHOD

Thirty-nine TSAs were performed for primary osteoarthritis by one surgeon using the same technique. For the glenoid side, a keeled, polyethylene, convex-backed component was implanted using the "cancellous compaction technique" consisting of minimal reaming, compaction bone grafting of the glenoid and minimal addition of cement. Postoperative clinical outcome was analysed using Constant scores and patient's subjective evaluation. Independent observers evaluated postoperative X-rays for radiolucent lines (RLL) around the base plate and keel.

RESULTS

At an average follow-up of 8.5 years (range 4.7-12.5), the Constant score improved from 33.5 to 73.0 points (P < 0.0001). Active anterior elevation improved from an average 95 ° to 140° (P < 0.0001), and active external rotation improved from 20° to 45° (P < 0.0001). Pain score improved from 3.1 to 13.6 (P < 0.0001). Radiologically, the RLL score increased from 1.09 (range, 0-3) postoperative to 5.7 (range, 0-18) (P < 0.0001) at final follow-up. The occurrence of definite radiological glenoid loosening was 15.5 %. Constant scores deteriorated with the progression of RLLs (P = 0.006). The rate of revision surgery for glenoid loosening was 2.5 %.

CONCLUSIONS

This study showed highly satisfactory clinical outcomes and low rates of revision for glenoid loosening using a bone-saving compaction technique for implantation of an all-polyethylene glenoid component.

摘要

目的

无菌性关节盂假体松动仍是全肩关节置换术(TSA)中常见的问题。本研究报告了采用“松质骨压实技术”植入关节盂假体后的长期前瞻性随访结果,以及该技术对临床疗效、透亮线(RLLs)的出现和进展的影响。

方法

由一名外科医生采用相同技术对39例原发性骨关节炎患者进行TSA手术。对于关节盂侧,使用“松质骨压实技术”植入带龙骨的聚乙烯凸背假体,该技术包括最小限度的扩孔、关节盂的压实植骨以及最少的骨水泥添加。术后临床疗效采用Constant评分和患者主观评价进行分析。独立观察者对术后X线片进行评估,观察基板和龙骨周围的透亮线(RLL)情况。

结果

平均随访8.5年(范围4.7 - 12.5年),Constant评分从33.5分提高到73.0分(P < 0.0001)。主动前举平均从95°提高到140°(P < 0.0001),主动外旋从20°提高到45°(P < 0.0001)。疼痛评分从3.1分提高到13.6分(P < 0.0001)。影像学上,RLL评分从术后的1.09(范围0 - 3)提高到末次随访时的5.7(范围0 - 18)(P < 0.0001)。明确的影像学关节盂松动发生率为15.5%。Constant评分随RLLs的进展而恶化(P = 0.006)。关节盂松动的翻修手术率为2.5%。

结论

本研究表明,采用保留骨的压实技术植入全聚乙烯关节盂假体,临床疗效高度满意,关节盂松动翻修率低。

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