首页> 外文期刊>Annals of the Rheumatic Diseases: A Journal of Clinical Rheumatology and Connective Tissue Research >Steroid injection for inferior heel pain: A randomised controlled trial
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Steroid injection for inferior heel pain: A randomised controlled trial

机译:适用于较低的鞋跟疼痛的类固醇注射:随机对照试验

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摘要

Background: Plantar fasciitis is a common cause of heel pain. The aim of this study was twofold: to compare steroid injection with placebo injection and to compare ultrasound guided with unguided steroid injection in the management of this condition. Methods: 65 patients with inferior heel pain were recruited between November 2008 and June 2011. Heel pain was measured using a visual analogue scale (VAS) at baseline and follow-up 6 and 12 weeks after injection. Results: 22 patients were randomised to ultrasound guided steroid injection, 21 patients to palpation guided steroid injection and 22 to ultrasound guided placebo injection. There was a significant difference in VAS scores between the groups at 6 and 12 weeks (p=0.018 and p=0.004, respectively). There was a 19.7 (95% CI 2.5 to 37.0) difference in mean VAS scores at 6 weeks between the ultrasound guided steroid group and the placebo group and a 24.0 (95% CI 6.6 to 41.3) difference between the unguided steroid group and the placebo group at 6 weeks. At 12 weeks, the mean difference was 25.1 (95% CI 6.5 to 43.6) and 28.4 (95% CI 11.1 to 45.7) respectively between both steroid injection groups and the placebo group. There was no difference in VAS scores following steroid injection between the ultrasound guided and the unguided groups at either time point. Plantar fascia thickness was significantly reduced after injection in both active treatment groups ( p=0.00). Conclusions: In this study, steroid injection showed a clear benefit over placebo at 6 weeks and this difference was maintained at 12 weeks. Trial Registration No ISRCTN79628180 (www.controlled-trials.com).
机译:背景:跖筋炎是脚跟疼痛的常见原因。本研究的目的是双重的:将类固醇注射与安慰剂注射进行比较,并在这种情况下使用无导体类固醇注入比较超声波引导。方法:2008年11月至2011年6月招聘了65例较低的鞋跟疼痛患者。使用基线的视觉模拟量表(VAS)测量后跟疼痛,并在注射后的后续6和12周。结果:22例患者被随机分为超声引导类固醇注射,21例患者触诊引导类固醇注射和22例超声引导安慰剂注射。在6和12周的组之间存在群体之间的VAS分数存在显着差异(P = 0.018和P = 0.004)。在超声引导类固醇组和安慰剂组之间的6周内,平均VAS分数有19.7(95%CI 2.5至37.0)差异,并在非控剂类固醇组和安慰剂之间的24.0(95%CI 6.6至41.3)之间的差异小组在6周。在12周,在类固醇注射组和安慰剂组之间,平均差异分别为25.1(95%CI 6.5至43.6)和28.4(95%CI 11.1至45.7)。在超声引导和在任一时点的非控件组之间的类固醇注射后VAS分数没有差异。在术中注射后,跖筋厚度明显减少(P = 0.00)。结论:在本研究中,类固醇注射在6周内对安慰剂进行了明显的益处,并且在12周内保持这种差异。试验登记没有ISRCTN79628180(www.controlled-trials.com)。

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    Department of Rheumatology Musgrave Park Hospital Belfast BT9 7JB United Kingdom;

    Department of Podiatry Belfast City Hospital Belfast United Kingdom;

    Centre for Public Health Queens' University Belfast Belfast United Kingdom;

    Department of Rheumatology Musgrave Park Hospital Belfast BT9 7JB United Kingdom;

    Department of Rheumatology Altnagelvin Area Hospital Londonderry United Kingdom;

    Department of Rheumatology Musgrave Park Hospital Belfast BT9 7JB United Kingdom;

    Department of Rheumatology Musgrave Park Hospital Belfast BT9 7JB United Kingdom;

    Department of Rheumatology Chapel Allerton Hospital Leeds United Kingdom;

    Department of Rheumatology Musgrave Park Hospital Belfast BT9 7JB United Kingdom;

    Department of Rheumatology Musgrave Park Hospital Belfast BT9 7JB United Kingdom;

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  • 正文语种 eng
  • 中图分类 免疫性疾病;
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