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超声引导下肌腱干针松解与切开松解治疗慢性肱骨外上髁炎的随机对照研究

Treatment of chronic lateral epicondylosis: a randomized trial comparing the efficacy of ultrasound-guided tendon dry needling and open-release surgery.

机构信息

Department of Radiology, Centre hospitalier de l'Université de Montréal (CHUM), 1000 rue Saint-Denis, Montreal, Quebec, H2X 0C1, Canada.

Research Center, Centre hospitalier de l'Université de Montréal (CHUM), 900 rue Saint-Denis, Montreal, Quebec, H2X 0A9, Canada.

出版信息

Eur Radiol. 2022 Nov;32(11):7612-7622. doi: 10.1007/s00330-022-08794-4. Epub 2022 Apr 28.

Abstract

OBJECTIVE

Evaluate the efficacy of ultrasound-guided dry needling and open-release surgery in reducing pain and improving function in workers with lateral epicondylosis refractory to at least 6 months of nonsurgical management.

METHODS

We randomly assigned participants in a 1:1 ratio to receive dry needling or surgery. The primary outcome was the Patient Rated Tennis Elbow Evaluation (PRTEE) score at 6 months. Secondary outcome measures examined the impact of these techniques on professional activity, grip strength, and Global Rating of Change and Satisfaction scales. Statistical analyses included mixed-effects models and Fisher's exact tests.

RESULTS

From October 2016 through June 2019, we enrolled 64 participants. Two participants were excluded, and data from 62 participants (48 ± 8 years, 33 men) with a mean duration of symptoms of 23 ± 21 months were analyzed. Baseline characteristics were similar in both groups. In the intention-to-treat analysis, no treatment-by-time interaction was observed (F = 0.72; p = .58). The least-squares mean difference from baseline in PRTEE scores at 6 months was 33.4 (CI 25.2 - 41.5) in the surgery group and 26.9 (CI 19.4 - 34.4) in the dry needling group (p = .25). The proportion of successful treatment was 83% (CI 63 - 95%) and 81% (CI 63 - 93%) in the surgery and dry needling groups, respectively (p = 1.00). Changes in secondary outcomes were in the same direction as those of the primary outcome. No adverse event occurred.

CONCLUSIONS

Ultrasound-guided dry needling resulted in comparable improvement in outcome scores on scales of pain, physical function, and global assessment of change and satisfaction than open-release surgery.

TRIAL REGISTRATION

ClinicalTrials.gov Identifier: NCT02710682 KEY POINTS: • In patients with chronic lateral epicondylosis, ultrasound-guided tendon dry needling provides comparable therapeutic efficacy to open-release surgery. • Ultrasound-guided tendon dry needling allows for an earlier return to work and may be less costly than open-release surgery. • Care management guidelines should recommend treatment by ultrasound-guided tendon dry needling before open-release surgery.

摘要

目的

评估超声引导下干针松解术与开放式松解手术在减轻疼痛和改善功能方面的疗效,这些患者患有外侧肱骨上髁炎,且对至少 6 个月的非手术治疗无反应。

方法

我们将参与者随机分配为 1:1 比例接受干针松解术或手术治疗。主要结局是 6 个月时的患者自评网球肘评估(PRTEE)评分。次要结局指标检查了这些技术对职业活动、握力和总体变化和满意度量表的影响。统计分析包括混合效应模型和 Fisher 精确检验。

结果

2016 年 10 月至 2019 年 6 月,我们共纳入 64 名参与者。排除了 2 名参与者,对 62 名参与者(48±8 岁,33 名男性)的数据进行了分析,这些参与者的症状持续时间平均为 23±21 个月。两组的基线特征相似。在意向治疗分析中,未观察到治疗与时间的交互作用(F=0.72,p=0.58)。手术组 6 个月时 PRTEE 评分的最小二乘均数差值为 33.4(CI 25.2-41.5),干针松解组为 26.9(CI 19.4-34.4)(p=0.25)。手术组和干针松解组的治疗成功率分别为 83%(CI 63-95%)和 81%(CI 63-93%)(p=1.00)。次要结局的变化方向与主要结局相同。没有不良事件发生。

结论

超声引导下干针松解术在疼痛、身体功能和整体变化和满意度量表上的疗效与开放式手术相当。

试验注册

ClinicalTrials.gov 标识符:NCT02710682

要点

  • 在患有慢性外侧肱骨上髁炎的患者中,超声引导下肌腱干针松解术与开放式松解手术相比,提供了相当的治疗效果。

  • 超声引导下肌腱干针松解术允许更早地恢复工作,并且可能比开放式松解手术更具成本效益。

  • 护理管理指南应建议在开放式松解手术之前进行超声引导下肌腱干针松解术治疗。

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