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300毫瓦、830纳米激光对慢性颈部疼痛的影响:一项双盲、随机、安慰剂对照研究。

The effect of 300 mW, 830 nm laser on chronic neck pain: a double-blind, randomized, placebo-controlled study.

作者信息

Chow Roberta T, Heller Gillian Z, Barnsley Les

机构信息

Castle Hill Medical Centre, 269-271 Old Northern Road, Castle Hill, NSW 2154, Australia.

出版信息

Pain. 2006 Sep;124(1-2):201-10. doi: 10.1016/j.pain.2006.05.018. Epub 2006 Jun 27.

Abstract

A randomized, double-blind, placebo-controlled study of low-level laser therapy (LLLT) in 90 subjects with chronic neck pain was conducted with the aim of determining the efficacy of 300 mW, 830 nm laser in the management of chronic neck pain. Subjects were randomized to receive a course of 14 treatments over 7 weeks with either active or sham laser to tender areas in the neck. The primary outcome measure was change in a 10 cm Visual Analogue Scale (VAS) for pain. Secondary outcome measures included Short-Form 36 Quality-of-Life questionnaire (SF-36), Northwick Park Neck Pain Questionnaire (NPNQ), Neck Pain and Disability Scale (NPAD), the McGill Pain Questionnaire (MPQ) and Self-Assessed Improvement (SAI) in pain measured by VAS. Measurements were taken at baseline, at the end of 7 weeks' treatment and 12 weeks from baseline. The mean VAS pain scores improved by 2.7 in the treated group and worsened by 0.3 in the control group (difference 3.0, 95% CI 3.8-2.1). Significant improvements were seen in the active group compared to placebo for SF-36-Physical Score (SF36 PCS), NPNQ, NPAD, MPQVAS and SAI. The results of the SF-36 - Mental Score (SF36 MCS) and other MPQ component scores (afferent and sensory) did not differ significantly between the two groups. Low-level laser therapy (LLLT), at the parameters used in this study, was efficacious in providing pain relief for patients with chronic neck pain over a period of 3 months.

摘要

对90名慢性颈部疼痛患者进行了一项随机、双盲、安慰剂对照的低强度激光疗法(LLLT)研究,目的是确定300毫瓦、830纳米激光治疗慢性颈部疼痛的疗效。受试者被随机分为两组,在7周内接受14次治疗,分别使用活性激光或假激光照射颈部的压痛部位。主要结局指标是10厘米视觉模拟量表(VAS)疼痛评分的变化。次要结局指标包括36项简短生活质量问卷(SF-36)、诺斯威克公园颈部疼痛问卷(NPNQ)、颈部疼痛与残疾量表(NPAD)、麦吉尔疼痛问卷(MPQ)以及通过VAS测量的自我评估疼痛改善情况(SAI)。在基线、7周治疗结束时以及基线后12周进行测量。治疗组的VAS疼痛平均评分改善了2.7分,而对照组恶化了0.3分(差异为3.0,95%CI为3.8 - 2.1)。与安慰剂组相比,活性组在SF-36身体评分(SF36 PCS)、NPNQ、NPAD、MPQ-VAS和SAI方面有显著改善。两组之间的SF-36心理评分(SF36 MCS)以及其他MPQ成分评分(传入和感觉)没有显著差异。在本研究中使用的参数下,低强度激光疗法(LLLT)在3个月内为慢性颈部疼痛患者提供疼痛缓解方面是有效的。

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