Electrical Stimulation and Cutaneous Wound Healing: A Review of Clinical Evidence

Sara Ud-Din, Ardeshir Bayat, Sara Ud-Din, Ardeshir Bayat

Abstract

Electrical stimulation (ES) has been shown to have beneficial effects in wound healing. It is important to assess the effects of ES on cutaneous wound healing in order to ensure optimization for clinical practice. Several different applications as well as modalities of ES have been described, including direct current (DC), alternating current (AC), high-voltage pulsed current (HVPC), low-intensity direct current (LIDC) and electrobiofeedback ES. However, no one method has been advocated as the most optimal for the treatment of cutaneous wound healing. Therefore, this review aims to examine the level of evidence (LOE) for the application of different types of ES to enhance cutaneous wound healing in the skin. An extensive search was conducted to identify relevant clinical studies utilising ES for cutaneous wound healing since 1980 using PubMed, Medline and EMBASE. A total of 48 studies were evaluated and assigned LOE. All types of ES demonstrated positive effects on cutaneous wound healing in the majority of studies. However, the reported studies demonstrate contrasting differences in the parameters and types of ES application, leading to an inability to generate sufficient evidence to support any one standard therapeutic approach. Despite variations in the type of current, duration, and dosing of ES, the majority of studies showed a significant improvement in wound area reduction or accelerated wound healing compared to the standard of care or sham therapy as well as improved local perfusion. The limited number of LOE-1 trials for investigating the effects of ES in wound healing make critical evaluation and assessment somewhat difficult. Further, better-designed clinical trials are needed to improve our understanding of the optimal dosing, timing and type of ES to be used.

Keywords: current; electrical stimulation; electrobiofeedback; treatment; wound healing; wounds.

Figures

Figure 1
Figure 1
A diagram to demonstrate some of the available treatment strategies for the management of chronic wounds including; compression bandaging, wound dressings, negative pressure wound therapy, ultrasound, debridement, skin substitute therapy and electrical stimulation.
Figure 2
Figure 2
Electrical stimulation (ES), in the form of alternating current (AC), direct current (DC) and pulsed current (PC), has been shown to have beneficial effects on cutaneous wound healing in chronic wounds. When ES is applied to a chronic wound, this produces beneficial effects throughout the three phases of wound healing: inflammation, proliferation and remodelling phases. Inflammatory phase: ES increases blood flow, tissue oxygenation and stimulates fibroblasts whilst reducing oedema and providing an increased antibacterial effect. Proliferative phase: ES increases membrane transport, collagen matrix organization, wound contraction and the stimulation of DNA and protein synthesis. Remodelling phase: ES increases epidermal cell proliferation, and migration as well as stimulation of fibroblasts thus enabling enhanced wound closure [19,20,21,22,23,24,25,26,27].
Figure 3
Figure 3
Electrical stimulation (ES), in the form of biofeedback ES, direct current (DC) and pulsed current (PC), has been shown to have beneficial effects on cutaneous wound healing in acute wounds. When ES is applied to an acute wound, this produces beneficial effects throughout the three phases of wound healing: inflammation, proliferation and remodelling phases. Inflammatory phase: ES increases blood flow, skin temperature and vasodilation. Proliferative phase: ES increases keratinocyte proliferation and wound contraction. Remodelling phase: ES advances the remodelling face and increases re-epithelialisation enabling enhanced wound healing [28,29,30,31,32,33,34].
Figure 4
Figure 4
The current of injury is thought to be significant in initiating repair. Undamaged human skin has an endogenous electrical potential and a transcutaneous current potential of 20–50 mV. This is generated by the movement of sodium ions through Na+/K+ ATPase pumps in the epidermis. The current of injury is generated through epithelial disruption. Following an injury to the skin, a flow of current through the wound pathway generates a lateral electrical field and this is termed the “current of injury” or “skin battery” effect.
Figure 5
Figure 5
Diagram demonstrating the various modes of application of electrical stimulation (ES). (a) Application of ES by electrodes placed near or on the wound site and connected to a device (this is the most common application of ES) [40]; (b) Application of a bioelectric dressing to the wound site [41]; (c) Wireless application of ES to a wound [42]; (d) Practitioner application of ES in the form electro biofeedback by the use of a device with an electrode placed in different areas around the wound site [43].
Figure 6
Figure 6
Illustrations showing one example of each of the various electrical waveforms available for the treatment of acute and chronic cutaneous wounds including alternating current, direct current, pulsed current and degenerate wave (please note that there are other subtypes of each of these waveforms).
Figure 7
Figure 7
A flowchart demonstrating the methodology and process of selecting relevant articles for review.
Figure 8
Figure 8
Graphical representation of the three phases of acute cutaneous wound healing and where the different waveforms of electrical stimulation are effective in each phase: inflammatory, proliferative and remodelling.

References

    1. Monaco J.L., Lawrence W.T. Acute wound healing: An overview. Clin. Plast. Surg. 2003;30:1–12. doi: 10.1016/S0094-1298(02)00070-6.
    1. Greaves N.S., Iqbal S.A., Baguneid M., Bayat A. The role of skin substitutes in the management of chronic cutaneous wounds. Wound Repair Regen. 2013;21:194–210. doi: 10.1111/wrr.12029.
    1. Fonder M.A., Lazarus G.S., Cowan D.A., Aronson-Cook B., Kohli A.R., Mamelak A.J. Treating the chronic wound: A practical approach to the care of nonhealing wounds and wound care dressings. J. Am. Acad. Dermatol. 2008;58:185–206. doi: 10.1016/j.jaad.2007.08.048.
    1. Singh A., Halder S., Chumber S., Misra M.C., Sharma L.K., Srivastava A. Meta-analysis of randomized controlled trials on hydrocolloid occlusive dressing versus conventional gauze dressing in the healing of chronic wounds. Asian J. Surg. 2004;27:326–332. doi: 10.1016/S1015-9584(09)60061-0.
    1. Posnett J., Franks P.J. The burden of chronic wounds in the UK. Nurs. Times. 2008;104:44–45.
    1. Mustoe T.A., O’Shaughnessy K., Kloeters O. Chronic wound pathogenesis and current treatment strategies: A unifying hypothesis. Plast. Reconstr. Surg. 2006;117:35S–41S. doi: 10.1097/01.prs.0000225431.63010.1b.
    1. Vileikyte L. Diabetic foot ulcers: A quality of life issue. Diabetes Metab. Res. Rev. 2001;17:246–249. doi: 10.1002/dmrr.216.
    1. Amsler F., Willenberg T., Blättler W. In search of optimal compression therapy for venous leg ulcers: A meta-anlysis of studies comparing divers bandages with specially designed stockings. J. Vasc. Surg. 2009;50:668–674. doi: 10.1016/j.jvs.2009.05.018.
    1. Carter J.M., Tingley-Kelley K., Warriner I.R.A. Silver treatments and silver-impregnated dressings for the healing of leg wounds and ulcers: A systematic review and meta-analysis. J. Am. Acad. Dermatol. 2010;63:668–679. doi: 10.1016/j.jaad.2009.09.007.
    1. Armstrong D.G., Marston W.A., Reyzelman A.M., Kirsner R.S. Comparison of negative pressure wound therapy with an ultraportable mechanically powered device vs. traditional electrically powered device for the treatment of chronic lower extremity ulcers: A multicenter randomized- controlled trial. Wound Repair Regen. 2011;19:173–180. doi: 10.1111/j.1524-475X.2010.00658.x.
    1. Cullum N.A., Al-Kurdi D., Bell-Syer S.E. Therapeutic ultrasound for venous leg ulcers. Cochrane Database Syst. Rev. 2010 doi: 10.1002/14651858.CD001180.pub3.
    1. Dumville J.C., Worthy G., Soares M.O., Bland J.M., Cullum N., Dowson C., Iglesias C., McCaughan D., Mitchell J.L., Nelson E.A., et al. VenUS II: A randomised controlled trial of larval therapy in the management of leg ulcers. Health Technol. Assess. 2009;13:1–206. doi: 10.3310/hta13550.
    1. Greaves N.S., Benatar B., Baguneid M., Bayat A. Single-stage application of a novel decellularized dermis for treatment-resistant lower limb ulcers: Positive outcomes assessed by SIAscopy, laser perfusion, and 3D imaging, with sequential timed histological analysis. Wound Repair Regen. 2013;21:813–822. doi: 10.1111/wrr.12113.
    1. Snyder R.J., Kirsner R.S., Warriner R.A., Lavery L.A., Hanft J.R., Sheehan P. Consensus recommendations on advancing the standard of care for treating neuropathic foot ulcers in patients with diabetes. Ostomy Wound Manag. 2010;56:S1–S24.
    1. Suh H., Petrofsky J., Fish A., Hernandez V., Mendoza E., Collins K., Yang T., Abdul A., Batt J., Lawson D. A new electrode design to improve outcomes in the treatment of chronic non-healing wounds in diabetes. Diabetes Technol. Ther. 2009;11:315–322. doi: 10.1089/dia.2008.0092.
    1. Petrofsky J., Lawson D., Prowse M., Suh H.J. Effects of a 2-, 3- and 4-electrode stimulator design on current dispersion on the surface and into the limb during electrical stimulation in controls and patients with wounds. J. Med. Eng. Technol. 2008;32:485–497. doi: 10.1080/03091900701574407.
    1. Jünger M., Arnold A., Zuder D., Stahl H.W., Heising S. Local therapy and treatment costs of chronic, venous leg ulcers with electrical stimulation (Dermapulse): A prospective, placebo controlled, double blind trial. Wound Repair Regen. 2008;16:480–487. doi: 10.1111/j.1524-475X.2008.00393.x.
    1. Isseroff R.R., Dahle S.E. Electrical stimulation therapy and wound healing: Where are we now? Adv. Wound Care. 2012;1:238–243. doi: 10.1089/wound.2011.0351.
    1. Reger S.I., Hyodo A., Negami S., Kambic H.E., Sahgal V. Experimental wound healing with electrical stimulation. Artif. Organs. 1999;23:460–462. doi: 10.1046/j.1525-1594.1999.06365.x.
    1. Gagnier K.A., Manix N., Baker L. The effects of electrical stimulation on cutaneous oxygen supply in paraplegics. Phys. Ther. 1988;68:835–839.
    1. Peters E.J., Armstrong D.G., Wunderlich R.P., Bosma J., Stacpoole-Shea S., Lavery L.A. The benefit of electrical stimulation to enhance perfusion in persons with diabetes mellitus. J. Foot Ankle Surg. 1998;37:396–400. doi: 10.1016/S1067-2516(98)80048-3.
    1. Rouabhia M., Park H., Meng S., Derbali H., Zhang Z. Electrical stimulation promotes wound healing by enhancing dermal fibroblast activity and promoting myofibroblast transdifferentiation. PLoS One. 2013;8:e71660. doi: 10.1371/journal.pone.0071660.
    1. Young S., Hampton S., Tadej M. Study to evaluate the effect of low-intensity pulsed electrical currents on levels of oedema in chronic non-healing wounds. J. Wound Care. 2011;20:370–373. doi: 10.12968/jowc.2011.20.8.368.
    1. Daeschlein G., Assadian O., Kloth L.C., Meinl C., Ney F., Kramer A. Antibacterial activity of positive and negative polarity low-voltage pulsed current (LVPC) on six typical gram-positive and gram-negative bacterial pathogens of chronic wounds. Wound Repair Regen. 2007;15:399–403. doi: 10.1111/j.1524-475X.2007.00242.x.
    1. Alvarez O.M., Mertz P.M., Smerbeck R.V., Eaglstein W.H. The healing of superficial skin wounds is stimulated by external electrical current. J. Invest. Dermatol. 1983;81:144–148. doi: 10.1111/1523-1747.ep12543498.
    1. Bourguignon G.J., Bourguignon L.Y. Electric stimulation of protein and DNA synthesis in human fibroblasts. FASEB J. 1987;1:398–402.
    1. Bassett C.A.L., Herrmann I. The effect of electrostatic fields on macromolecular synthesis by fibroblasts in vitro. J. Cell Biol. 1968;9:39.
    1. Cramp A.F.L., Gilsenan C., Lowe A.S., Walsh D.M. The effect of high- and low-frequency transcutaneous electrical nerve stimulation upon cutaneous blood flow and skin temperature in healthy subjects. Clin. Physiol. 2000;20:150–157. doi: 10.1046/j.1365-2281.2000.00240.x.
    1. Cramp A.F., Noble J.G., Lowe A.S., Walsh D.M. Transcutaneous electrical nerve stimulation (TENS): The effect of electrode placement upon cutaneous blood flow and skin temperature. Acupunct. Electrother. Res. 2001;26:25–37.
    1. Cramp F.L., McCullough G.R., Lowe A.S., Walsh D.M. Transcutaneous electric nerve stimulation: The effect of intensity on local and distal cutaneous blood flow and skin temperature in healthy subjects. Arch. Phys. Med. Rehabil. 2002;83:5–9. doi: 10.1053/apmr.2002.27478.
    1. Kaada B., Olsen E., Eielsen O. In search of mediators of skin vasodilation induced by transcutaneous nerve stimulation: III. Increase in plasma VIP in normal subjects and in Raynaud’s disease. Gen. Pharmacol. 1984;15:107–113. doi: 10.1016/0306-3623(84)90091-0.
    1. Kaada B., Helle K.B. In search of mediators of skin vasodilation induced by transcutaneous nerve stimulation: IV. In vitro bioassay of the vasoinhibitory activity of sera from patients suffering from peripheral ischemia. Gen. Pharmacol. 1984;15:115–122.
    1. Abram S.E., Asiddao C.B., Reynolds A.C. Increased skin temperature during transcutaneous electrical stimulation. Anesth. Analg. 1980;59:22–25.
    1. Sebastian A., Syed F., Perry D., Balamurugan V., Colthurst J., Chaudhry I.H., Bayat A. Acceleration of cutaneous healing by electrical stimulation: Degenerate electrical waveform down-regulates inflammation, up-regulates angiogenesis and advances remodelling in temporal punch biopsies in a human volunteer study. Wound Repair Regen. 2011;19:693–708. doi: 10.1111/j.1524-475X.2011.00736.x.
    1. Szuminky N.J., Albers A.C., Unger P., Eddy J.G. Effect of narrow, pulsed high voltages on bacterial viability. Phys. Ther. 1994;74:660–667.
    1. Foulds I.S., Barker A.T. Human skin battery potentials and their possible role in wound healing. Br. J. Dermatol. 1983;109:515–522. doi: 10.1111/j.1365-2133.1983.tb07673.x.
    1. McGinnis M.E., Vanable J.W., Jr. Voltage gradients in newt limb stumps. Prog. Clin. Biol. Res. 1986;210:213–238.
    1. Barker A.T., Jaffe L.F., Vanable J.W., Jr. The glabrous epidermis of cavies contains a powerful battery. Am. J. Physiol. 1982;242:R358–R366.
    1. Thakral G., Lafontaine J., Najafi B., Talal T.K., Kim P., Lavery L.A. Electrical stimulation to accelerate wound healing. Diabet. Foot Ankle. 2013 doi: 10.3402/dfa.v4i0.22081.
    1. Atalay C., Yilmaz K.B. The effect of transcutaneous electrical nerve stimulation on postmastectomy skin flap necrosis. Breast Cancer Res. Treat. 2009;117:611–614. doi: 10.1007/s10549-009-0335-z.
    1. Blount A.L., Foster S., Rapp D.A., Wilcox R. The use of bioelectric dressings in skin graft harvest sites: A prospective case series. J. Burn Care Res. 2012;33:354–357. doi: 10.1097/BCR.0b013e31823356e4.
    1. Wirsing P.G., Habrom A.D., Zehnder T.M., Friedli S., Blatti M. Wireless micro current stimulation—An innovative electrical stimulation method for the treatment of patients with leg and diabetic foot ulcers. Int. Wound J. 2013 doi: 10.1111/iwj.12204.
    1. Ud-Din S., Perry D., Giddings P., Colthurst J., Zaman K., Cotton S., Whiteside S., Morris J., Bayat A. Electrical stimulation increases blood flow and haemoglobin levels in acute cutaneous wounds without affecting wound closure time: Evidenced by non-invasive assessment of temporal biopsy wounds in human volunteers. Exp. Dermatol. 2012;21:758–764. doi: 10.1111/j.1600-0625.2012.00361.x.
    1. Stillings D. A survey of the history of electrical stimulation for pain to 1900. Med. Instrum. 1975;9:255–259.
    1. Kloth L.C., Feedar J.A. Acceleration of wound healing with high voltage, monophasic, pulsed current. Phys. Ther. 1988;68:503–508.
    1. Carley P.J., Wainapel S.F. Electrotherapy for acceleration of wound healing: Low intensity direct current. Arch. Phys. Med. Rehabil. 1985;66:443–446.
    1. Sebastian A., Syed F., McGrouther D.A., Colthurst J., Paus R., Bayat A. A novel in vitro assay for electrophysiological research on human skin fibroblasts: Degenerate electrical waves downregulate collagen I expression in keloid fibroblasts. Exp. Dermatol. 2011;20:64–68. doi: 10.1111/j.1600-0625.2010.01150.x.
    1. Perry D., Colthurst J., Giddings P., McGrouther D.A., Morris J., Bayat A. Treatment of symptomatic abnormal skin scars with electrical stimulation. J. Wound Care. 2010;19:447–453.
    1. Kloth L.C. Electrical stimulation technologies for wound healing. Adv. Wound Care. 2014;3:81–90. doi: 10.1089/wound.2013.0459.
    1. Feedar J.A., Kloth L.C., Gentzkow G.D. Chronic dermal ulcer healing enhanced with monophasic pulsed electrical stimulation. Phys. Ther. 1991;71:639–649.
    1. Gentzkow G.D., Alon G., Taler G.A., Eltorai I.M., Montroy R.E. Healing of refactory stage III and IV pressure ulcers by a new electrical stimulation device. Wounds. 1993;5:160–172.
    1. Baker L.L., Chanbers R., Demuth S.K., Villar F. Effects of electrical stimulation on wound healing in patients with diabetic ulcers. Diabetes Care. 1997;20:405–412. doi: 10.2337/diacare.20.3.405.
    1. Franek A., Kostur R., Polak A., Taradaj J., Szlachta Z., Blaszczak E., Dolibog P., Dolibog P., Koczy B., Kucio C. Using high voltage electrical stimulation in the treatment of recalcitrant pressure ulcers: Results of a randomised, controlled clinical study. Ostomy Wound Manag. 2012;58:30–44.
    1. Griffin J.W., Tooms R.E., Mendius R.A., Clifft J.K., Vander Zwaag R., el-Zeky F. Efficacy of high voltage pulsed current for healing of pressure ulcers in patients with spinal cord injury. Phys. Ther. 1991;71:433–442.
    1. Houghton P.E., Campbell K.E., Fraser C.H., Harris C., Keast D.H., Potter P.J., Hayes K.C., Woodbury M.G. Electrical stimulation therapy increases rate of healing of pressure ulcers in community-dwelling people with spinal cord injury. Arch. Phys. Med. Rehabil. 2010;91:669–678. doi: 10.1016/j.apmr.2009.12.026.
    1. Peters E.J., Lavery L.A., Armstrong D.G., Fleischli J.G. Electric stimulation as an adjunct to heal diabetic foot ulcers: A randomized clinical trial. Arch. Phys. Med. Rehabil. 2001;82:721–725. doi: 10.1053/apmr.2001.23780.
    1. Houghton P.E., Kincaid C.B., Lovell M., Campbell K.E., Keast D.H., Woodbury M.G., Harris K.A. Effect of electrical stimulation on chronic leg ulcer size and appearance. Phys. Ther. 2003;83:17–28.
    1. Burdge J.J., Hartman J.F., Wright M.L. A study of HVPC as an adjunctive therapy in limb salvage for chronic diabetic wounds of the lower extremity. Ostomy Wound Manag. 2009;55:30–38.
    1. Goldman R., Rosen M., Brewley B., Golden M. Electrotherapy promotes healing and microcirculation of infrapopliteal ischemic wounds: A prospective pilot study. Adv. Skin Wound Care. 2004;17:284–294. doi: 10.1097/00129334-200407000-00010.
    1. Ahmad E.T. High-voltage pulsed galvanic stimulation: Effect of treatment duration on healing of chronic pressure ulcers. Mediterr. Counc. Burn. Fire Disasters. 2008;21:124–128.
    1. Gault W.R., Gatens P.F., Jr. Use of low intensity direct current in management of ischemic skin ulcers. Phys. Ther. 1976;56:265–269.
    1. Wood J.M., Evans P.E., 3rd, Schallreuter K.U., Jacobson W.E., Sufit R., Newman J., White C., Jacobson M. A multicenter study on the use of pulsed low-intensity direct current for healing chronic stage II and stage III decubitus ulcers. Arch. Dermatol. 1993;129:999–1009. doi: 10.1001/archderm.1993.01680290071011.
    1. Nolan M.F., Hartsfield J.K., Witters D.M., Wason P.J. Failure of transcutaneous electrical nerve stimulation in the conventional and burst modes to alter digital skin temperature. Arch. Phys. Med. Rehabil. 1993;74:182–187.
    1. Simpson K.H., Ward J. A Randomized, double-blind, crossover study of the use of transcutaneous spinal electroanalgesia in patients with pain from chronic critical limb ischemia. J. Pain Symptom Manag. 2004;28:511–516.
    1. Wikstrom S.O., Svedman P., Svensson H., Tanweer A.S. Effect of transcutaneous nerve stimulation on microcirculation in intact skin and blister wounds in healthy volunteers. Scand. J. Plast. Reconstr. Surg. Hand Surg. 1999;33:195–201. doi: 10.1080/02844319950159451.
    1. Janković A., Binić I. Frequency rhythmic electrical modulation system in the treatment of chronic painful leg ulcers. Arch. Dermatol. Res. 2008;300:377–383. doi: 10.1007/s00403-008-0875-9.
    1. Santamato A., Panza F., Fortunato F., Portincasa A., Frisardi V., Cassatella G., Valente M., Seripa D., Ranieri M., Fiore P. Effectiveness of the frequency rhythmic electrical modulation system for the treatment of chronic and painful venous leg ulcers in older adults. Rejuvenation Res. 2012;15:281–287. doi: 10.1089/rej.2011.1236.
    1. Ud-Din S., Giddings P., Colthurst J., Whiteside S., Morris J., Bayat A. Significant reduction of symptoms of scarring with electrical stimulation: Evaluated with subjective and objective assessment tools. Wounds. 2013;25:212–224.
    1. Hampton S., King L. Healing an intractable wound using bio-electric stimulation therapy. Br. J. Nurs. 2005;14:S30–S32. doi: 10.12968/bjon.2005.14.Sup3.18608.
    1. Hampton S., Collins F. Treating a pressure ulcer with bio-electric stimulation therapy. Br. J. Nurs. 2006;15:S14–S18. doi: 10.12968/bjon.2006.15.Sup1.20687.
    1. Franek A., Taradaj J., Polak A., Cierpka L., Blaszczak E. Efficacy of high voltage stimulation for healing of venous leg ulcers in surgically and conservatively treated patients. Phlebologie. 2006;35:127–133.
    1. Kloth L.C. Wound healing with conductive electrical stimulation—It’s the dosage that counts. J. Wound Technol. 2009;6:30.
    1. Ramadan A., Elsaidy M., Zyada R. Effect of low-intensity direct current on the healing of chronic wounds: A literature review. J. Wound Care. 2008;17:292–296. doi: 10.12968/jowc.2008.17.7.30520.
    1. Newton R.A., Karselis T.C. Skin pH following high voltage pulsed galvanic stimulation. Phys. Ther. 1983;63:1593–1596.
    1. Ojingwa J.C., Isseroff R.R. Electrical stimulation of wound healing. J. Investig. Dermatol. 2003;121:1–12. doi: 10.1046/j.1523-1747.2003.12454.x.
    1. Adunsky A., Ohry A. Decubitus direct current treatment (DDCT) of pressure ulcers: Results of a randomized double-blinded placebo controlled study. Arch. Gerontol. Geriatr. 2005;41:261–269. doi: 10.1016/j.archger.2005.04.004.
    1. Chen C., Johnson M.I. A comparison of transcutaneous electrical nerve stimulation (TENS) at 3 and 80 pulses per second on cold-pressor pain in healthy human participants. Clin. Physiol. Funct. Imaging. 2010;30:260–268. doi: 10.1111/j.1475-097X.2010.00936.x.
    1. Liebano R.E., Rakel B., Vance C.G., Walsh D.M., Sluka K.A. An investigation of the development of analgesic tolerance to TENS in humans. Pain. 2011;152:335–342. doi: 10.1016/j.pain.2010.10.040.
    1. Kjartansson J., Lundeberg T., Körlof B. Transcutaneous electrical nerve stimulation (TENS) in ischemic tissue. Plast. Reconstr. Surg. 1988;81:813–815.
    1. Johnson M.I. Transcutaneous Electrical Nerve Stimulation (TENS) In: Watson T., editor. Electrotherapy: Evidence-Based Practice. 12th ed. Elsevier; Toronto, ON, Canada: 2008.
    1. Sherry J.E., Oehrlein K.M., Hegge K.S., Morgan B.J. Effect of burst-mode transcutaneous electrical nerve stimulation on peripheral vascular resistance. Phys. Ther. 2001;81:1183–1191.
    1. Colthurst J., Giddings P. A retrospective case note review of the Fenzian electrostimulation system: A novel non-invasive, non-pharmacological treatment. Pain Clin. 2007;19:7–14. doi: 10.1179/016911107X217446.
    1. Guo A., Song B., Reid B., Gu Y., Forrester J.V., Jahoda C.A., Zhao M. Effects of physiological electric fields on migration of human dermal fibroblasts. J. Investig. Dermatol. 2010;130:2320–2327. doi: 10.1038/jid.2010.96.
    1. Talebi G., Torkaman G., Firoozabadi M., Shariat S. Effect of anodal and cathoda microamperage direct current electrical stimulation on injury potential and wound size in guinea pigs. J. Rehabil. Res. Dev. 2008;45:153–159. doi: 10.1682/JRRD.2007.05.0068.
    1. Koel G., Houghton P.E. Electrostimulation: Current status, strength of evidence guidelines, and meta-analysis. Adv. Wound Care (New Rochelle) 2014;3:118–126. doi: 10.1089/wound.2013.0448.

Source: PubMed

3
Iratkozz fel