Randomized Double-Blind Sham-Controlled Crossover Study of Short-Term Effect of Percutaneous Electrical Nerve Stimulation in Neuropathic Pain

被引:19
作者
Raphael, Jon H. [1 ]
Raheem, Tarek A.
Southall, Jane L. [2 ]
Bennett, Alan [3 ]
Ashford, Robert L.
Williams, Sharon [3 ]
机构
[1] Birmingham City Univ, Fac Hlth, Grad Sch, Birmingham B15 3TN, W Midlands, England
[2] Russells Hall Hosp, Dudley, England
[3] Kidderminster Treatment Ctr, Kidderminster, England
关键词
Chronic Pain; CRPS; Percutaneous Electrical Nerve Stimulation (PENS); Neuromodulation; Neuropathic Pain; LOW-BACK-PAIN; ANALGESIC RESPONSE; NEUROMODULATION THERAPY; OLDER-ADULTS; MANAGEMENT; EFFICACY;
D O I
10.1111/j.1526-4637.2011.01215.x
中图分类号
R614 [麻醉学];
学科分类号
100217 ;
摘要
Background. Percutaneous electrical nerve stimulation (PENS) is an electrical neuromodulation technique that has shown its therapeutic potential in various chronic pain conditions over the past few years, but well-blinded controlled studies are lacking. Patients and Methods. A randomized double-blind sham-controlled crossover trial on 31 patients with chronic pain with surface hyperalgesia to investigate the efficacy of PENS. Results. For the active PENS therapies, the median numerical rating scale (NRS) for pain changed from 7.5 (standard deviation [SD] +/- 1) (range 6-10) before therapy to 0.5 (range 0-8.5) after therapy (Z = -4.206, P < 0.0005 [two-tailed]). The mean pain pressure threshold (PPT) measured with the von Frey aesthesiometer changed from 202 gm (SD +/- 137 gm) (range 55-800 gm) before therapy to 626 gm (SD +/- 228 gm) (range 45-800 gm) after therapy (Z = -4.373, P < 0.0005 [two-tailed]). There was a statistically significant difference between the changes in NRS for the active (3.9 [+/- 3.2] [0-8]) compared with the sham (0.1 [+/- 0.4] [0-1.5]) therapies, U = 40, Z = -3.484, P < 0.0001 (two-tailed). There was a statistically significant difference between the changes in PPT for the active (310 gm [+/- 267 gm] [0-670 gm]) compared with the sham (8 gm [+/- 4 gm] [0-15 gm]) therapies, U = 48.5, Z = -2.699, P = 0.007 (two-tailed). Conclusion. PENS therapy appears to be effective in providing short-term pain relief in chronic pain conditions. Studies, involving larger sample sizes and longer follow-up are recommended.
引用
收藏
页码:1515 / 1522
页数:8
相关论文
共 16 条
[1]   Use of percutaneous electrical nerve stimulation (PENS) in the short-term management of headache [J].
Ahmed, HE ;
White, PF ;
Craig, WF ;
Hamza, MA ;
Ghoname, ESA ;
Gajraj, NM .
HEADACHE, 2000, 40 (04) :311-315
[2]   Percutaneous electrical nerve stimulation: An alternative to antiviral drugs for acute herpes zoster [J].
Ahmed, HE ;
Craig, WF ;
White, PF ;
Ghoname, ESA ;
Hamza, MA ;
Gajraj, NM ;
Taylor, SM .
ANESTHESIA AND ANALGESIA, 1998, 87 (04) :911-914
[3]  
Borg-Stein Joanne, 2003, Pain Pract, V3, P125, DOI 10.1046/j.1533-2500.2003.03019.x
[4]   The effect of stimulus frequency on the analgesic response to percutaneous electrical nerve stimulation in patients with chronic low back pain [J].
Ghoname, EA ;
Craig, WF ;
White, PF ;
Ahmed, HE ;
Hamza, MA ;
Gajraj, NM ;
Vakharia, AS ;
Noe, CE .
ANESTHESIA AND ANALGESIA, 1999, 88 (04) :841-846
[5]   Percutaneous electrical nerve stimulation: an alternative to TENS in the management of sciatica [J].
Ghoname, EA ;
White, PF ;
Ahmed, HE ;
Hamza, MA ;
Craig, WF ;
Noe, CE .
PAIN, 1999, 83 (02) :193-199
[6]   Percutaneous electrical nerve stimulation for low back pain - A randomized crossover study [J].
Ghoname, ESA ;
Craig, WF ;
White, PF ;
Ahmed, HE ;
Hamza, MA ;
Henderson, BN ;
Gajraj, NM ;
Huber, PJ ;
Gatchel, RJ .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1999, 281 (09) :818-823
[7]  
GOLDSTEIN A, 1989, MOL PHARMACOL, V36, P265
[8]   Percutaneous electrical nerve stimulation - A novel analgesic therapy for diabetic neuropathic pain [J].
Hamza, MA ;
White, PF ;
Craig, WF ;
Ghoname, EA ;
Ahmed, HE ;
Proctor, TJ ;
Noe, CE ;
Vakharia, AS ;
Gajraj, N .
DIABETES CARE, 2000, 23 (03) :365-370
[9]  
Johnson M., 2002, Electrotherapy: evidence-based practice, V11th, P259
[10]  
SEROUSSI RE, 2003, PAIN PRACT, V3, P22