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用于拇指腕掌关节关节炎的缝线纽扣悬吊成形术:至少2年随访

Suture-button suspensionplasty for thumb carpometacarpal arthritis: a minimum 2-year follow-up.

作者信息

Yao Jeffrey, Song Yohan

机构信息

Department of Orthopaedic Surgery, Stanford University Medical Center, Redwood City, CA 94063, USA.

出版信息

J Hand Surg Am. 2013 Jun;38(6):1161-5. doi: 10.1016/j.jhsa.2013.02.040. Epub 2013 May 3.

Abstract

PURPOSE

To retrospectively review the results at a minimum of 2 years of suture-button plasty with partial or full trapeziectomy and suture-button suspensionplasty.

METHODS

We evaluated 21 patients who received suture-button suspensionplasty at least 2 years after surgery. We measured postoperative pinch strength, grip strength, range of motion, and metacarpal height. All patients also completed the Quick Disabilities of the Arm, Shoulder, and Hand questionnaire.

RESULTS

At an average follow-up of 2.8 ± 0.7 years, the mean Quick Disabilities of the Arm, Shoulder, and Hand score was 10 ± 9. Pinch and grip strengths were 86% and 89% of the contralateral limb, respectively. Average first trapezial height was 74% of the contralateral trapezial height. There were no major complications.

CONCLUSIONS

The favorable results of the suture-button suspensionplasty procedure confirm its usefulness in treating thumb carpometacarpal arthritis with minimal risk of complications, ineffective fixation, or loss of function. Subjective and objective outcomes measures are similar to previously described techniques. The benefit of this technique results from the implanted nature of the suspensionplasty elements that require no time to heal, so rehabilitation is begun as early as 10 days postoperatively.

TYPE OF STUDY/LEVEL OF EVIDENCE: Therapeutic IV.

摘要

目的

回顾性分析部分或全大多角骨切除术联合缝线纽扣悬吊成形术至少2年的治疗结果。

方法

我们评估了21例术后至少2年接受缝线纽扣悬吊成形术的患者。我们测量了术后捏力、握力、活动范围和掌骨高度。所有患者还完成了手臂、肩部和手部快速残疾问卷。

结果

平均随访2.8±0.7年,手臂、肩部和手部快速残疾问卷平均得分为10±9。捏力和握力分别为对侧肢体的86%和89%。第一大多角骨平均高度为对侧大多角骨高度的74%。无重大并发症。

结论

缝线纽扣悬吊成形术的良好结果证实了其在治疗拇指腕掌关节炎方面的有效性,并发症风险、固定无效或功能丧失的风险最小。主观和客观结果测量与先前描述的技术相似。该技术的优势源于悬吊成形术元件的植入特性,无需愈合时间,因此术后最早10天即可开始康复治疗。

研究类型/证据水平:治疗性IV级。

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