首页> 外文期刊>European spine journal: official publication of the European Spine Society, the European Spinal Deformity Society, and the European Section of the Cervical Spine Research Society >Can we predict response to the McKenzie method in patients with acute low back pain? A secondary analysis of a randomized controlled trial
【24h】

Can we predict response to the McKenzie method in patients with acute low back pain? A secondary analysis of a randomized controlled trial

机译:我们可以预测急性下腰痛患者对McKenzie方法的反应吗?随机对照试验的次要分析

获取原文
获取原文并翻译 | 示例
           

摘要

Purpose: To evaluate whether patients' treatment preferences, characteristics, or symptomatic response to assessment moderated the effect of the McKenzie method for acute low back pain (LBP). Methods: This study involved a secondary analysis of a previous RCT on the effect of adding the McKenzie method to the recommended first-line care for patients with acute non-specific LBP. 148 patients were randomized to the First-line Care Group (recommended first-line care alone) or the McKenzie Group (McKenzie method in addition to the first-line care) for a 3-week course of treatment. The primary outcome was pain intensity at 3 weeks. The ability of six patient characteristics to identify those who respond best to McKenzie method was assessed using interaction terms in linear regression models. Results: The six investigated potential effect modifiers for response to the McKenzie method did not predict a more favorable response to this treatment. None of the point estimates for effect modification met our pre-specified criterion of clinical importance of a 1 point greater improvement in pain. For five of the six predictors, the 95% CI did not include our criterion for meaningful clinical improvement. Conclusion: We were unable to find any clinically useful effect modifiers for patients with acute LBP receiving the McKenzie method.
机译:目的:评估患者的治疗偏好,特征或对评估的症状反应是否减轻了McKenzie方法对急性下背痛(LBP)的影响。方法:本研究包括对先前的RCT的辅助分析,该分析涉及在急性非特异性LBP患者的推荐一线治疗中添加McKenzie方法的效果。 148例患者被随机分为一线护理组(仅推荐一线护理)或麦肯齐组(除一线护理外采用麦肯锡方法),为期3周。主要结局是3周时的疼痛强度。使用线性回归模型中的交互项评估了六个患者特征识别对McKenzie方法最有效的患者的能力。结果:研究的六种对McKenzie方法反应的潜在效应修饰剂并未预测对该治疗有更好的反应。效果改善的得分估计均未达到我们预先指定的临床重要性标准,即疼痛改善1分。对于六个预测变量中的五个,95%CI不包括我们有意义的临床改善的标准。结论:我们没有发现任何接受McKenzie方法治疗的急性LBP患者的临床有用的调节剂。

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

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