首页> 美国卫生研究院文献>British Medical Journal >Comparison of fluoroscopically guided and blind corticosteroid injections for greater trochanteric pain syndrome: multicentre randomised controlled trial
【2h】

Comparison of fluoroscopically guided and blind corticosteroid injections for greater trochanteric pain syndrome: multicentre randomised controlled trial

机译:荧光镜引导下和盲目的皮质类固醇激素注射治疗大转子转子疼痛综合征的比较:多中心随机对照试验

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

>Objective To determine whether fluoroscopic guidance improves outcomes of injections for greater trochanteric pain syndrome.>Design Multicentre double blind randomised controlled study.>Setting Three academic and military treatment facilities in the United States and Germany.>Participants 65 patients with a clinical diagnosis of greater trochanteric pain syndrome.>Interventions Injections of corticosteroid and local anaesthetic into the trochanteric bursa, using fluoroscopy (n=32) or landmarks (that is, “blind” injections; n=33) for guidance.>Main outcome measures Primary outcome measures: 0-10 numerical rating scale pain scores at rest and with activity at one month (positive categorical outcome predefined as ≥50% pain reduction either at rest or with activity, coupled with positive global perceived effect). Secondary outcome measures included Oswestry disability scores, SF-36 scores, reduction in drug use, and patients’ satisfaction.>Results No differences in outcomes occurred favouring either the fluoroscopy or blind treatment groups. One month after injection the average pain scores were 2.7 at rest and 5.0 with activity in the fluoroscopy group compared with 2.2 and 4.0 in the blind injection group. Three months after the injection, 15 (47%) patients in the blind group and 13 (41%) in the fluoroscopy group continued to have a positive outcome.>Conclusion Although using fluoroscopic guidance dramatically increases treatment costs for greater trochanteric pain syndrome, it does not necessarily improve outcomes.>Trial registration Clinical trials
机译:>目的:确定透视指导是否可以改善大转子转子疼痛综合征的注射效果。>设计多中心双盲随机对照研究。>设置三项学术和军事意义美国和德国的治疗机构。>参与者 65例临床诊断为股骨转子大疼痛综合征的患者。>干预用荧光检查法将皮质类固醇和局部麻醉剂注入股骨转子(n = 32)或界标(即“盲注”; n = 33)作为指导。>主要结局指标主要结局指标:0-10个数字量表,分别用于休息和运动时的疼痛评分在一个月内(积极的分类结果预定义为在休息或活动时疼痛减轻≥50%,加上积极的整体感知效果)。次要结果指标包括Oswestry残疾评分,SF-36评分,药物使用减少和患者满意度。>结果无论是透视检查还是盲法治疗,结果均无差异。注射后一个月,透视组的平均疼痛评分为休息时为2.7,活动时为5.0,而盲注组为2.2和4.0。注射后三个月,盲组的15例患者(47%)和透视检查组的13例患者(41%)继续取得了积极的结果。>结论股骨转子疼痛综合征,并不一定能改善预后。>试验注册临床试验

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号