Pain Management Center, Harvard Medical School, Brigham and Women's Hospital, Chestnut Hill, Massachusetts, U.S.A.
Pain Pract. 2019 Jun;19(5):466-475. doi: 10.1111/papr.12764. Epub 2019 Feb 4.
This controlled trial examined the benefit of a high-frequency transcutaneous electrical nerve stimulation (hfTENS) device (the Quell, NeuroMetrix, Inc., Waltham, MA, U.S.A.) for patients with chronic low back pain (CLBP).
Thirty-five (n = 35) participants were randomly assigned to use the device each day for 3 months (experimental group) and were compared with 33 subjects without the device (treatment-as-usual control group). All patients were instructed to complete baseline questionnaires and were assessed on thresholds of pressure pain and mechanical temporal summation as part of standardized quantitative sensory testing (QST). The subjects also uploaded smartphone applications (apps) for tracking use of the hfTENS and for daily pain assessment. Each participant completed weekly phone interviews, was prompted to complete daily pain app assessments, and was asked to repeat the baseline questionnaires again after 6 weeks and 3 months.
Sixty percent of the subjects were female, 77.9% were Caucasian, and the average age was 46.2 years. Significant reductions in pain intensity (P < 0.01) and activity interference (P < 0.025) and significant improvements in pain catastrophizing (P < 0.025) were noted in the experimental group compared with the control group. No group differences were found on depression, anxiety, or pain-related disability. Older subjects with a longer duration of pain tended to use the hfTENS more often. Subjects who showed greater sensitivity based on QST results revealed increased use of the hfTENS (P < 0.025) and tended to believe that the hfTENS was more helpful in reducing their back pain, but these findings did not reach significance (P = 0.09).
These results suggest that hfTENS can have a moderate effect in reducing pain and improving quality of life in low back pain patients. Further trials designed to determine the mechanism of action of the hfTENS are needed.
本对照试验旨在研究高频经皮神经电刺激(hfTENS)设备(美国马萨诸塞州沃尔瑟姆市 NeuroMetrix 公司的 Quell)对慢性腰痛(CLBP)患者的益处。
35 名(n=35)参与者被随机分配每天使用该设备 3 个月(实验组),并与 33 名未使用该设备的受试者(常规治疗对照组)进行比较。所有患者均被要求完成基线问卷,并进行压力痛觉阈值和机械时间总和的定量感觉测试(QST)。受试者还上传了智能手机应用程序(app),用于跟踪 hfTENS 的使用情况和日常疼痛评估。每位参与者完成每周电话访谈,被提示完成每日疼痛 app 评估,并在 6 周和 3 个月后再次完成基线问卷。
60%的受试者为女性,77.9%为白种人,平均年龄为 46.2 岁。与对照组相比,实验组的疼痛强度(P < 0.01)和活动干扰(P < 0.025)显著降低,疼痛灾难化(P < 0.025)显著改善。在抑郁、焦虑或疼痛相关残疾方面,两组间无差异。疼痛持续时间较长的老年患者更倾向于使用 hfTENS。根据 QST 结果显示敏感性更高的受试者增加了 hfTENS 的使用(P < 0.025),并倾向于认为 hfTENS 更有助于减轻腰痛,但这些发现没有达到显著水平(P = 0.09)。
这些结果表明,hfTENS 可在一定程度上减轻腰痛患者的疼痛并提高生活质量。需要进一步的试验来确定 hfTENS 的作用机制。