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超声引导下类固醇注射治疗肩部疼痛的对照试验。

A controlled trial of the benefits of ultrasound-guided steroid injection for shoulder pain.

机构信息

Service de rhumatologie, DAL, CHUV, avenue Pierre-Decker 4, 1011 Lausanne, Switzerland.

出版信息

Joint Bone Spine. 2012 Mar;79(2):166-9. doi: 10.1016/j.jbspin.2011.04.001. Epub 2011 May 25.

Abstract

OBJECTIVES

We studied the value of ultrasound (US) to define shoulder pathology and guide local steroid injection in comparison with a standard injection in the management of the acute painful shoulder.

METHODS

Seventy consecutive patients with acute shoulder pain were assessed clinically and by US. Patients were randomized to receive either a standard subacromial infiltration of 7 mg of betamethasone or a US-guided injection according to the US diagnosis. Follow-up evaluations were performed by an independent assessor who was blinded to the results of the initial US and clinical assessments.

RESULTS

Sixty-seven patients completed the study. Both groups showed a significant reduction in both daytime and night pain compared to baseline. The US injection group had significantly less pain at rest at 2 and 6 weeks (NRS: 1.6 vs 3.3, P<0.005; 3 vs 4.2, P<0.04). The percentage of good responders was significantly higher in US group at 2 weeks, (81% vs 54%, P<0.005) and 6 weeks (64% vs 38%, P<0.05). At 2 and 6 weeks, responder rate and activity pain scores as well as Constant score were in favour of US, though did not reach statistical significance.

CONCLUSION

Local steroid injection for shoulder pain leads to significant improvements in pain and function for up to 12 weeks. An US examination to define the origin of shoulder pain as well as to guide injection provides significant additional benefits for up to 6 weeks. We recommend routine US examination as part of the management of acute shoulder pain.

摘要

目的

我们研究了超声(US)在定义肩部病变和指导局部皮质类固醇注射方面的价值,并与标准注射方法在急性肩部疼痛患者中的管理进行了比较。

方法

连续评估 70 例急性肩部疼痛患者的临床和 US 表现。患者随机接受标准肩峰下注射(7mg 倍他米松)或根据 US 诊断进行 US 引导下注射。由一位独立评估者进行随访评估,该评估者对初始 US 和临床评估结果均不知情。

结果

67 例患者完成了研究。两组患者在日间和夜间疼痛方面均较基线时显著减轻。US 注射组在 2 周和 6 周时静息时疼痛明显减轻(NRS:1.6 对 3.3,P<0.005;3 对 4.2,P<0.04)。US 组在 2 周(81%对 54%,P<0.005)和 6 周(64%对 38%,P<0.05)时的良好反应者比例明显更高。在 2 周和 6 周时,反应率、活动疼痛评分和 Constant 评分均有利于 US 组,但未达到统计学意义。

结论

局部皮质类固醇注射治疗肩部疼痛可显著改善疼痛和功能,持续 12 周。US 检查可明确肩部疼痛的来源并指导注射,可在 6 周内提供显著的额外益处。我们建议将常规 US 检查作为急性肩部疼痛管理的一部分。

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