...
首页> 外文期刊>BMC Complementary and Alternative Medicine >Association of lumbar spine stiffness and flexion-relaxation phenomenon with patient-reported outcomes in adults with chronic low back pain – a single-arm clinical trial investigating the effects of thrust spinal manipulation
【24h】

Association of lumbar spine stiffness and flexion-relaxation phenomenon with patient-reported outcomes in adults with chronic low back pain – a single-arm clinical trial investigating the effects of thrust spinal manipulation

机译:成人慢性下腰痛的腰椎僵硬和屈曲放松现象与患者报告的结局的关系–一项单臂临床试验,研究推力脊柱操纵的影响

获取原文
           

摘要

Background Spinal manipulation (SM) is used commonly for treating low back pain (LBP). Spinal stiffness is routinely assessed by clinicians performing SM. Flexion-relaxation ratio (FRR) was shown to distinguish between LBP and healthy populations. The primary objective of this study was to examine the association of these two physiological variables with patient-reported pain intensity and disability in adults with chronic LBP (>12?weeks) receiving SM. Methods A single-arm trial provided 12 sessions of side-lying thrust SM in the lumbosacral region over 6?weeks. Inclusion criteria included 21–65?years old, Roland-Morris Disability Questionnaire (RMDQ) score?≥?6 and numerical pain rating score?≥?2. Spinal stiffness and FRR were assessed pre-treatment at baseline, after 2?weeks and after 6?weeks of treatment. Lumbar spine global stiffness (GS) were calculated from the force-displacement curves obtained using i) hand palpation, ii) a hand-held device, and iii) an automated indenter device. Lumbar FRR was assessed during trunk flexion-extension using surface electromyography. The primary outcomes were RMDQ and pain intensity measured by visual analog scale (VAS). Mixed-effects regression models were used to analyze the data. Results The mean age of the 82 participants was 45?years; 48% were female; and 84% reported LBP >1?year. The mean (standard deviation) baseline pain intensity and RMDQ were 46.1 (18.1) and 9.5 (4.3), respectively. The mean reduction (95% confidence interval) after 6?weeks in pain intensity and RMDQ were 20.1?mm (14.1 to 26.1) and 4.8 (3.7 to 5.8). There was a small change over time in the palpatory GS but not in the hand-held or automated GS, nor in FRR. The addition of each physiologic variable did not affect the model-estimated changes in VAS or RMDQ over time. There was no association seen between physiological variables and LBP intensity. Higher levels of hand-held GS at L3 and automated GS were significantly associated with higher levels of RMDQ ( p =?0.02 and 0.03, respectively) and lower levels of flexion and extension FRR were significantly associated with higher levels of RMDQ ( p =?0.02 and 0.008, respectively) across the 3 assessment time points. Conclusions Improvement in pain and disability observed in study participants with chronic LBP was not associated with the measured GS or FRR. Trial registration NCT01670292 on clinicaltrials.gov, August 2, 2012
机译:背景技术脊柱操纵(SM)通常用于治疗腰痛(LBP)。脊柱僵硬通常由执行SM的临床医生评估。屈曲松弛比(FRR)被证明可以区分LBP和健康人群。这项研究的主要目的是研究在接受LSM治疗的慢性LBP(> 12周)成人中这两个生理变量与患者报告的疼痛强度和残疾之间的关系。方法单臂试验在6周内在腰provided部提供12次侧卧式推力SM。入选标准包括21-65岁,Roland-Morris残疾问卷(RMDQ)得分≥6和数字疼痛评分得分≥2。在基线治疗前,治疗2周和6周后评估脊柱僵硬和FRR。腰椎整体刚度(GS)是根据使用i)触诊,ii)手持设备和iii)自动压头设备获得的力-位移曲线计算得出的。使用表面肌电图评估躯干屈伸过程中的腰椎FRR。主要结果是RMDQ和通过视觉模拟量表(VAS)测量的疼痛强度。混合效果回归模型用于分析数据。结果82名参与者的平均年龄为45岁。女性占48%; 84%的人认为LBP> 1?year。基线疼痛强度和RMDQ的平均值(标准差)分别为46.1(18.1)和9.5(4.3)。 6周后疼痛强度和RMDQ的平均降低幅度(95%置信区间)分别为20.1mm(14.1至26.1)和4.8(3.7至5.8)。触诊GS随时间的变化很小,但手持或自动GS或FRR都没有变化。每个生理变量的添加都不会影响模型估计的VAS或RMDQ随时间的变化。生理变量与LBP强度之间没有关联。 L3和自动GS的手持GS水平较高与RMDQ较高水平(分别为p =?0.02和0.03)显着相关,而屈曲和伸展FRR较低水平与RMDQ较高水平显着相关(p =? 3个评估时间点分别为0.02和0.008)。结论在慢性LBP研究参与者中观察到的疼痛和残疾改善与测量的GS或FRR无关。于2012年8月2日在Clinicaltrials.gov上进行NCT01670292试验注册

著录项

相似文献

  • 外文文献
  • 中文文献
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