Xia Ting, Long Cynthia R, Vining Robert D, Gudavalli Maruti R, DeVocht James W, Kawchuk Gregory N, Wilder David G, Goertz Christine M
Palmer Center for Chiropractic Research, Palmer College of Chiropractic, 741 Brady Street, Davenport, IA, 52803, USA.
Department of Physical Therapy, University of Alberta, Edmonton, AB, Canada.
BMC Complement Altern Med. 2017 Jun 9;17(1):303. doi: 10.1186/s12906-017-1821-1.
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.
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.
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.
Improvement in pain and disability observed in study participants with chronic LBP was not associated with the measured GS or FRR.
NCT01670292 on clinicaltrials.gov, August 2, 2012.
脊柱推拿(SM)常用于治疗腰痛(LBP)。临床医生在进行脊柱推拿时会常规评估脊柱僵硬程度。研究表明,屈伸松弛率(FRR)可区分腰痛患者和健康人群。本研究的主要目的是探讨这两个生理变量与接受脊柱推拿的慢性腰痛(>12周)成人患者自我报告的疼痛强度和功能障碍之间的关联。
一项单臂试验在6周内提供12次腰骶部侧卧推法脊柱推拿。纳入标准包括年龄在21 - 65岁之间、罗兰·莫里斯功能障碍问卷(RMDQ)评分≥6且数字疼痛评分≥2。在治疗前的基线、治疗2周后和6周后评估脊柱僵硬程度和FRR。腰椎整体僵硬程度(GS)通过使用以下方法获得的力 - 位移曲线计算得出:i)手部触诊、ii)手持设备、iii)自动压头设备。在躯干屈伸过程中使用表面肌电图评估腰椎FRR。主要结局指标为RMDQ和视觉模拟量表(VAS)测量的疼痛强度。使用混合效应回归模型分析数据。
82名参与者的平均年龄为45岁;48%为女性;84%报告腰痛>1年。平均(标准差)基线疼痛强度和RMDQ分别为46.1(18.1)和9.5(4.3)。6周后疼痛强度和RMDQ的平均降低值(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随时间有小的变化,但手持或自动GS以及FRR没有变化。添加每个生理变量均未影响模型估计的VAS或RMDQ随时间的变化。生理变量与腰痛强度之间未发现关联。在三个评估时间点,L3处较高水平的手持GS和自动GS分别与较高水平的RMDQ显著相关(p分别为0.02和0.03),较低水平的屈伸FRR分别与较高水平的RMDQ显著相关(p分别为0.02和0.008)。
慢性腰痛研究参与者中观察到的疼痛和功能障碍改善与测量的GS或FRR无关。
clinicaltrials.gov上的NCT01670292,2012年8月2日。