首页> 外文期刊>The clinical journal of pain >Validity of cross-friction algometry procedure in referred muscle pain syndromes: preliminary results of a new referred pain provocation technique with the aid of a Fischer pressure algometer in patients with nonspecific low back pain.
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Validity of cross-friction algometry procedure in referred muscle pain syndromes: preliminary results of a new referred pain provocation technique with the aid of a Fischer pressure algometer in patients with nonspecific low back pain.

机译:交叉摩擦法测量方法在参考性肌肉疼痛综合征中的有效性:借助非费力腰痛患者的Fischer压力计,一项新的参考疼痛激发技术的初步结果。

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OBJECTIVES: Deep cross-friction pressure with a finger or an elbow in the proximal gluteal region causes a sciaticlike pain along the side of the thigh and the leg as a clinical presence of referred pain (RP) in patients with nonspecific low back pain (LBP). This study investigated the reliability and discriminative ability of experimentally provoked RP as a result of deep cross-friction with the aid of a Fischer algometer. The new clinical examination method measures the provoked RP threshold resulting in an outcome, expressed in kg/cm2. METHODS: Forty two patients with subacute LBP (3 to 12 wk) participated in a prospective clinical trial. The outcome was assessed by means of the standard (perpendicular) pressure pain thresholds (PPT) measured with the aid of a Fischer algometer on both sides of the gluteus medius, the provoked RP pain thresholds (PPT-RP) at the location of the medial superior cluneal nerve, the Oswestry Disability Index , and the McGill Pain Questionnaire. The diagnostic criteria for the clinical presence of RP were determined by the patient on the pain chart drawings of the McGill Pain Questionnaire. The criteria for provoked RP were determined by means of PPT-RP with the aid of a Fischer algometer until the patient pointed out the RP zone in the thigh and/or the leg. RESULTS: The interobserver reliability was sufficient for both sides with and without RP (intraclass correlation coefficient>0.97). The test-retest performed independently of the observers ranking, showed a perfect reliability of the PPT-RP measurements (intraclass correlation coefficient>0.98). The PPT-RP at the level of the medial superior cluneal nerve in the subgroup with a clinical presence of RP (N=20) was significantly higher (3.5 kg/cm2) than in the subgroup patients without RP (N=22). The correlation between the factor RP and the PPT-RP was high (R=0.91, P<0.001). The clinically important difference between provoked and clinical presence of RP was found to be higher or lower than 5.6 kg/cm2. The standard PPT measurement of the gluteus medius revealed no significant differences between the subgroups with and without RP. CONCLUSIONS: This clinical study support the reliability and discriminative ability of a new method of experimentally provoked RP, using deep cross-friction pressure with the aid of a Fischer algometer in patients with LBP. The experimentally "provoked referred pain threshold" (PPT-RP) values lower than 6 kg/cm correspond clinically with the presence of a referred muscle pain area in the thigh and/or the leg. Further studies of a similar kind are nevertheless needed to confirm those conclusions and to assess the responsiveness of the provoked RP measurements in different treatment follow-up periods.
机译:目的:在非特异性下背痛(LBP)患者中,在大腿和小腿附近用手指或肘部施加较大的交叉摩擦压力会导致大腿和小腿侧面发生坐骨神经痛)。这项研究调查了通过费歇尔(Fischer)测力计进行深度交叉摩擦后,实验激发的RP的可靠性和判别能力。新的临床检查方法测量诱发的RP阈值,以产生结果,以kg / cm2表示。方法:42例亚急性LBP(3至12周)患者参加了一项前瞻性临床试验。通过在臀中侧两侧的Fischer血压计测量的标准(垂直)压力疼痛阈值(PPT),在内侧位置引起的RP疼痛阈值(PPT-RP)来评估结果阴唇上神经,Oswestry残疾指数和McGill疼痛问卷。 RP在临床上的诊断标准由患者在McGill疼痛问卷的疼痛图表上确定。借助Fischer血凝仪通过PPT-RP确定激发RP的标准,直到患者指出大腿和/或腿部的RP区。结果:观察者之间的可靠性对于有和没有RP的双方都足够(组内相关系数> 0.97)。独立于观察者排名的重测,显示了PPT-RP测量的完美可靠性(类内相关系数> 0.98)。临床上存在RP的亚组(N = 20)的内侧上腓神经的PPT-RP显着高于无RP的亚组患者(N = 22)(3.5 kg / cm2)。因子RP与PPT-RP之间的相关性很高(R = 0.91,P <0.001)。发现诱发性和临床存在的RP之间的重要临床差异高于或低于5.6 kg / cm2。臀中肌的标准PPT测量显示,有和没有RP的亚组之间无显着差异。结论:这项临床研究支持一种新的实验性RP方法的可靠性和判别能力,该方法是通过深费摩压力在Fischer algometer的帮助下对LBP患者采用深摩擦力。低于6 kg / cm的实验性“诱发性参考疼痛阈值”(PPT-RP)值在临床上对应于大腿和/或腿中存在参考肌肉疼痛区域。尽管如此,仍需要进行类似类型的进一步研究,以证实这些结论并评估在不同的治疗随访期内激发的RP测量的反应性。

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