SAInT 研究:使用前外侧与后侧方法注射类固醇治疗肩峰下疼痛综合征的随机对照试验方案。

IF 2.8 Q1 ORTHOPEDICS
Charalambos P Charalambous, John T Hirst, Tariq Kwaees, Suzanne Lane, Clare Taylor, Nilesh Solanki, Alex Maley, Rebecca Taylor, Laura Howell, Stephen Nyangoma, Francis L Martin, Maqsood Khan, Muhammad N Choudhry, Vishwanath Shetty, Rayaz A Malik
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引用次数: 0

摘要

目的:类固醇注射用于治疗肩峰下疼痛综合征,可通过前外侧或后侧方法注射到肩峰下间隙。目前尚不清楚哪种方法能更好地改善临床症状和功能。这是一项随机对照试验(RCT)的方案,目的是比较通过前外侧或后侧方法在肩峰下间隙注射类固醇的临床效果:肩峰下间隙注射试验(SAInT)是一项单中心、平行、双臂随机对照试验。参与者将按 1:1 的比例被分配到通过前外侧或后侧方法进行肩峰下间隙类固醇注射。然后,两个试验组的参与者都将接受物理治疗,作为治疗肩峰下疼痛综合征的标准护理方法。主要分析将比较注射后三个月牛津肩关节评分(OSS)的变化。次要结果包括注射后 6 个月和 12 个月时牛津肩关节评分的变化,以及注射后 3 个月、6 个月和 1 年时疼痛数字评定量表(0 = 无痛,10 = 疼痛最严重)、手臂、肩部和手部残疾问卷 (DASH) 和 36 项短式健康调查 (SF-36) (RAND)。还将对注射过程中的疼痛进行评估。至少将招募 86 名患者,以获得 80% 的力量来检测注射后三个月时两组患者在 OSS 变化上 6 个点的最小重要差异:这项试验的结果将证明肩峰下疼痛综合征患者在肩峰下间隙注射类固醇后,前外侧入路与后侧入路在肩部疼痛和功能方面是否存在差异。这将有助于指导肩峰下疼痛综合征患者的治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The SAInT study: a protocol for a randomized controlled trial of steroid injection for subacromial pain syndrome using the anterolateral versus posterior approach.

Aims: Steroid injections are used for subacromial pain syndrome and can be administered via the anterolateral or posterior approach to the subacromial space. It is not currently known which approach is superior in terms of improving clinical symptoms and function. This is the protocol for a randomized controlled trial (RCT) to compare the clinical effectiveness of a steroid injection given via the anterolateral or the posterior approach to the subacromial space.

Methods: The Subacromial Approach Injection Trial (SAInT) study is a single-centre, parallel, two-arm RCT. Participants will be allocated on a 1:1 basis to a subacromial steroid injection via either the anterolateral or the posterior approach to the subacromial space. Participants in both trial arms will then receive physiotherapy as standard of care for subacromial pain syndrome. The primary analysis will compare the change in Oxford Shoulder Score (OSS) at three months after injection. Secondary outcomes include the change in OSS at six and 12 months, as well as the Pain Numeric Rating Scale (0 = no pain, 10 = worst pain), Disabilities of Arm, Shoulder and Hand questionnaire (DASH), and 36-Item Short-Form Health Survey (SF-36) (RAND) at three months, six months, and one year after injection. Assessment of pain experienced during the injection will also be determined. A minimum of 86 patients will be recruited to obtain an 80% power to detect a minimally important difference of six points on the OSS change between the groups at three months after injection.

Conclusion: The results of this trial will demonstrate if there is a difference in shoulder pain and function after a subacromial space steroid injection between the anterolateral versus posterior approach in patients with subacromial pain syndrome. This will help to guide treatment for patients with subacromial pain syndrome.

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来源期刊
Bone & Joint Open
Bone & Joint Open ORTHOPEDICS-
CiteScore
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8 weeks
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