Microcurrent Stimulation for Macular Degeneration

Microcurrent stimulation is a technique to apply electrical stimulation to nerve fibers using cutaneous electrodes. Microcurrent stimulation of the macula has been used to treat patients with age-related macular degeneration (AMD), utilizing currents on the order of 50 to 500 microamperes. This procedure is also known as transcutaneous electrical stimulation of the macula (TESMAC). A primary purpose of electrical stimulation, using higher millicurrents as in transcutaneous electrical nerve stimulation (TENS) treatment, has been to relieve pain. It has also been reported in use for increasing circulation, promoting closure of bone fractures and improving wound healing.

CONCLUSIONS

The Task Force on Complementary Therapies believes that, based on available evidence in the peer-reviewed literature, strong scientific evidence has not been found to demonstrate the effectiveness of microcurrent stimulation for AMD. Long-term studies with larger samples of patients, well-described patient selection criteria, adequate control groups, and standardized follow-up and outcome measures are critical to establishing a base of evidence regarding effectiveness.

BENEFITS

There are two uncontrolled studies published in a non-peer reviewed journal comprising 71 patients with AMD, who were treated with both nutritional supplements and electrical stimulation and one uncontrolled study published in a non-peer reviewed journal of 43 patients with macular degeneration treated only with electrical stimulation. The studies reported that some patients had improved visual acuity after treatment.

RISKS

Overall, the rate of adverse effects from microcurrent stimulation or TENS is reported as low. Adverse incidents are related to electrode placement. There may be a significant financial risk associated with the costs of these treatments over a long period of time.

INFORMATION FOR PATIENTS

Physicians can advise their patients contemplating microcurrent stimulation for AMD to ask the following questions of their provider:

  • Is the treatment being provided as part of an FDA-authorized study?
  • What are the results and benefits compared to a control group (a group not receiving microcurrent stimulation)?
  • What other treatment options are available and how do they compare?
  • Is lifelong treatment with microcurrent stimulation necessary to maintain benefits?

REPORT

DESCRIPTION OF THE TECHNOLOGY

Microcurrent stimulation is a technique to apply electrical stimulation to nerve fibers using cutaneous electrodes. Microcurrent stimulation for macular degeneration is described as applying 200 microamperes of electricity from a nine-volt battery to eight points around the eye. This technique utilizes lower currents, on the order of 50 to 500 microamperes. The device controller provides the microcurrent using two different waveforms and four frequencies.

In comparison, transcutaneous electrical nerve stimulation (TENS) is a technique to apply millicurrents to nerve fibers using cutaneous electrodes. Short pulses of electrical current last from 9 to 350 microseconds, and are applied at frequencies of 0.3 to 294 MHz. The device controls provide for adjustment in the pulse parameters. The primary application of TENS in health care has been to relieve pain. Other reported uses include increasing circulation, enhancing closure of bone fractures, and improving wound healing.

MECHANISM OF ACTION

For age-related macular degeneration (AMD), the postulated mechanism is that microcurrent stimulation improves membrane permeability, nerve conduction velocity, protein synthesis, and adenosine triphosphate (ATP) levels. In a very small experimental study (n= 9), microcurrent stimulation was shown to increase microcirculatory blood flow in intact skin and blister wounds, as measured by red blood cell velocity.[1] In an animal study, direct electric currents were shown to increase ATP concentrations in tissues and stimulate amino acid transport into rat skin.[2]

DEFINITION OF THE PROBLEM

Microcurrent stimulation of the macula has been proposed as treatment for patients with AMD. Age-related macular degeneration is the leading cause of irreversible severe central visual loss in Caucasian Americans 50 years and older. Typically, patients who progress to the neovascular form of the disease or have geographic atrophy involving the foveal center tend to develop severe vision loss. Laser photocoagulation, photodynamic therapy with verteporfin, and specific nutritional supplements are treatments that have demonstrated efficacy in randomized controlled trials for certain stages of AMD.

FDA STATUS

Although it has been reported by VisionWorks, Inc. (New Paltz, NY) that the Macular Degeneration Foundation plans to propose an industry-sponsored double-masked, randomized and multisite clinical trial for microcurrent stimulation of the macula for submittal to the U.S. Food and Drug Administration (FDA), this is not confirmed by the Macular Degeneration Foundation website.

Microcurrent stimulation devices currently marketed in the U.S. do not have FDA premarket approval for the indication of macular degeneration. At this time, any research studies in the U.S. using microcurrent stimulation for macular degeneration require FDA authorization and Institutional Review Board approval.[3]

SUMMARY OF EVIDENCE

Search Methods and Study Selection

In August 2000, the Academy searched through MEDLINE and EMBASE in the English language from January 1970 to August 2000 for articles relating to TENS, microcurrent stimulation, and ocular conditions. No articles were identified, but a bibliographic search of related articles identified one study for the application of electrical stimulation in patients with AMD.[4] This article was found in a non-peer reviewed journal.

To update the assessment, in March 2004 a search of MEDLINE and EMBASE was conducted for the period January 1968 through February 2004, with the same search strategy. No new citations were identified. Using the author names from the paper identified earlier, an Internet search using the Google search engine, located another paper in a non-peer reviewed journal.[5] The Internet search found a web site (www.mdsupport.org) which contained a discussion of microcurrent stimulation. Through this source an additional paper was identified.[6]

Statistical Issues and Study Design

Two studies found were case series, one with 25 patients[4] and the other with 46 patients.[5] The treatment in both studies was microcurrent stimulation and nutritional supplements. Another case series was of 43 patients treated with microcurrent stimulation. These studies have the following limitations: small study population, no control population, lack of detailed documentation on patient selection and patients who declined treatment, and lack of standardized outcome measures other than visual acuity. The two studies of microcurrent stimulation and nutritional supplements also have the limitation of insufficient methodology to distinguish between the results of antioxidant supplementation and microcurrent stimulation.

Information about the effect of an intervention should be obtained by comparing a treated group with an untreated control group similar in all the important respects. One way to assure similarity between the two groups is to use randomization. Because case series have no control group and do not use randomization, there is no way to estimate how an intervention might have changed an outcome. In addition, case series usually describe a small number of patients. Small sample sizes can lead to patient-selection bias as well as a higher likelihood that the observed effect was a result of chance. Properly documented case series can provide important insights into the potential utility of a new treatment and be valuable for those designing appropriate controlled clinical trials. Necessary documentation includes details about the patient selection criteria, the number of patients who declined surgery, and how the enrolled patients compared to the patients who refused treatment. Use of standardized follow-up intervals and outcomes assessment would further improve the quality of information, as would comparisons to the natural history of the remaining, untreated patient population. There should be appropriate study controls, such as using sham microcurrent stimulation treatment or using the fellow eye as a control.

BENEFITS

The proposed benefits are that visual acuity is improved. In order to maintain the effects, microcurrent stimulation therapy is presumed to be ongoing or lifelong, although maintenance intervals are proposed to be less frequent than the initial treatment phase.

One study of 25 patients with AMD, aged 48 to 79 years, reported the results of both nutritional supplementation and electrical stimulation.[4] Patients were treated for varying intervals, from 2 years to 7 years with a daily multivitamin and mineral supplement, and a monthly administration of electrical treatment of 200 microamperes on the closed eyelid for 7 minutes for each eye. There was no control population for comparison purposes.

The study reported the following results: 15 patients improved their visual acuity, and 10 patients had reduced acuity. The overall group lost an average of 0.30 letters of visual acuity over an average treatment period of 4.0 years.[4]

A second paper reported on two series of patients.[5] One series of 12 patients with AMD, aged 60 to 89 years, were followed for up to 6 years and treated with nutritional supplements and microcurrent stimulation once a week for 6 weeks. The second series of 34 patients with AMD, aged 61 to 87 years, were followed for up to 6 years and treated with nutritional supplements and microcurrent stimulation several times a week. There was no control population in either series for comparison purposes. The machines used delivered 200 microamperes at ±9 volts of alternating, square wave current. The series of 12 patients showed an average loss of 3 letters of visual acuity over a 2-year period. The series of 34 patients had an average gain of 8.5 letters of acuity per eye.[5]

A third paper reported on a series of 43 patients (65 eyes) with macular degeneration treated with direct microcurrent of 200 microamperes for 20 minutes for 36 sessions.[6] The treatment was applied for 10 minutes per eye three to four times a week. No details of patients’ ages or length of time of follow up was given. Thirty-five of 65 eyes (54%) had a 1 to 4 line improvement in visual acuity, 35% had no improvement, and 8% had a decline.

RISKS

The overall rate of adverse effects from electrical stimulation appears to be low. In the studies of AMD and microcurrent stimulation, there were no reported adverse effects from the electrical stimulation. Adverse effects could include: electrical burns if electrodes are not coupled to conductive gel, dermatitis, and skin irritation at the electrode sites with repeated application. Some materials reviewed during the Internet search indicate that patients may self-apply the electrical stimulation, in which case there may be risks of incorrect application. There may also be risks if the current applied is higher than what has been studied. There may be a significant financial risk associated with the costs of these treatments over a long period of time.

QUESTIONS FOR SCIENTIFIC INQUIRY

  • What is the biological basis for microcurrent stimulation for treating AMD?
  • Does microcurrent stimulation reduce visual loss caused by AMD, using randomized controlled clinical trials in larger, well-designed studies with adequate statistical analyses, standardized outcome measures and sufficient follow-up intervals?
  • How effective is microcurrent stimulation compared to standard therapies for AMD, i.e., laser surgery and photodynamic therapy?

INFORMATION FOR PATIENTS

Physicians can advise their patients contemplating microcurrent stimulation for AMD to ask the following questions of their provider:

  • Is the treatment being provided as part of an FDA-authorized study?
  • What are the results and benefits compared to a control group (a group not receiving microcurrent stimulation)?
  • What other treatment options are available and how do they compare?
  • Is lifelong treatment with microcurrent stimulation necessary to maintain benefits?

CONCLUSIONS

Based on available evidence in the peer-reviewed scientific literature, the Task Force on Complementary Therapies believes that strong scientific evidence has not been found to demonstrate the effectiveness of microcurrent stimulation treatment of AMD compared to standard therapies. Long-term studies with larger samples of patients, well-described patient selection criteria, adequate control groups, and standardized follow-up and outcome measures are critical to establishing a base of evidence regarding effectiveness.

DEVELOPMENT OF COMPLEMENTARY THERAPY ASSESSMENTS

Complementary, or alternative therapies, are a growing part of health care in America. Americans spend an estimated $14 billion a year on alternative treatments. Mainstream medicine is recognizing a need to learn more about alternative therapies and determine their true value. Most medical schools in the United States offer courses in alternative therapies. The editors of the Journal of the American Medical Association announced that publishing research on alternative therapies will be one of its priorities. The National Institutes of Health National Center for Complementary and Alternative Medicine has broadly defined complementary and alternative medicine as those treatments and health care practices not taught widely in medical schools, not generally used in hospitals, and not usually reimbursed by medical insurance companies. More scrutiny and scientific objectivity is being applied to determine whether evidence supporting their effectiveness exists.

In the fall of 1998, the Board of Trustees appointed a Task Force on Complementary Therapy to evaluate complementary therapies in eye care and develop an opinion on their safety and effectiveness, based on available scientific evidence, in order to inform ophthalmologists and their patients. A scientifically grounded analysis of the data will help ophthalmologists and patients evaluate the research and thus make more rational decisions on appropriate treatment choices.

The Academy believes that complementary therapies should be evaluated similarly to traditional medicine: evidence of safety, efficacy, and effectiveness should be demonstrated.[7,8] Many therapies used in conventional medical practice also have not been as rigorously tested as they should be. Given the large numbers of patients affected and the health care expenditures involved it is important that data and scientific information be used to base all treatment recommendations. In this way, we can encourage high-quality, rigorous research on complementary therapies.[9-11]

Ideally, a study of efficacy compares a treatment to a placebo or another treatment, using a double-masked controlled trial and well-defined protocol. Reports should describe enrollment procedures, eligibility criteria, clinical characteristics of the patients, methods for diagnosis, randomization method, definition of treatment, control conditions, and length of treatment. They should also use standardized outcomes and appropriate statistical analyses.

The goal of these assessments is to provide objective information of complementary therapies and provide a scientific basis for physicians to advise their patients, when asked.

To accomplish these goals, the assessments, in general, are intended to do the following:

  • Describe the scientific rationale or mechanism for action for the complementary therapy.
  • Describe the methods and basis for collecting evidence.
  • Describe the relevant evidence.
  • Summarize the benefits and risks of the complementary therapy.
  • Pose questions for future research inquiry.
  • Summarize the evidence on safety and effectiveness.

REFERENCES

  1. Wikstrom SO, Svedman P, Svensson H, Tanweer AS. 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.
  2. Cheng N, Van Hoof H, Bock E et al. The effects of electric currents on ATP generation, protein synthesis and membrane transport in rat skin. Clinical Orthopedics and Related Research 1982: 71:264-71.
  3. Rosenthal AR. FDA Position on Microcurrent Stimulation. Letter to the Editor. EyeNet Magazine 2004;1:8.
  4. Michael LD, Allen MJ. Nutritional supplementation, electrical stimulation and age-related macular degeneration. J of Orthomolecular Medicine 1993; 8:168-71.
  5. Allen MJ, Jarding JB, Zehner R. Macular degeneration treatment with nutrients and micro current electricity. J of Orthomolecular Medicine 1998;13:211-14.
  6. Wallace L. The treatment of macular degeneration and other retinal diseases using bioelectromagnetics therapy. J of Optometric Phototherapy March 1997;4-5.
  7. Fontanarosa PB, Lundberg GD. Alternative medicine meets science (editorial). JAMA 1998; 280: 1618-19.
  8. DeAngelis CD, Fontanarosa PB. Drugs alias dietary supplements. JAMA 2003;290:1519-20.
  9. Marcus DM, Grollman AP. Botanical medicines–the need for new regulations. N Engl J Med 2002;347:2073-6.
  10. Margolin A, Avants SK, Kleber HD. Investigating alternative medicine therapies in randomized controlled trials (editorial). JAMA 1998; 280:1626-8.
  11. Miller FG, Emanuel EJ, Rosenstein, DL, Straus SE. Ethical issues concerning research in complementary and alternative medicine. JAMA 2004;291:599-604.

Prepared by the American Academy of Ophthalmology Complementary Therapy Task Force

  • Ivan R. Schwab, MD, Chair William F. Mieler, MD
  • Roger Husted, MD Sayoko E. Moroi, MD, PhD
  • Jeffrey Todd Liegner, MD Denise Satterfield, MD
  • Harold P. Koller, MD Peter R. Holyk, MD, Consultant

Academy Staff:

  • Flora C. Lum, MD
  • Nancy Collins, RN, MPH

Approved by the Quality of Care Secretariat September 15, 2000

Approved by the Quality of Care and Knowledge Base Development Secretariat March 31, 2004

Copyright © 2000, 2004

American Academy of Ophthalmology

All rights reserved.

Microcurrent Facial Toning – What is it & How Does it Work?

As “baby boomers” age, more advancements are being made in anti-aging products to meet their needs. Electronic facial machines, which are designed to tighten and tone sagging facial muscles, are no exception.

The latest facial toning machines use “microcurrent” technology and are one of the hottest things in the anti-aging industry right now. There’s a good reason that these machines are so popular. Using microcurrent impulses, they give almost instant, visible results to tighten, tone, and firm aging skin. In fact, the results from microcurrent facial toning are so dramatic that they are often referred to as “non surgical face lifts”.

Just how does microcurrent facial toning work? To understand that, we first need to understand what causes our facial skin to wrinkle and sag. As we age, our muscles become accustomed to certain expressions and tend to “stick” in these positions. A great example of this is the furrow between the eyebrows that many people get. At the same time, other muscles in our face are hardly ever used, and they begin to atrophy, which leads to sagging. An example of this can often be seen around our jaw lines, chins and necks where we tend to develop sagging or loss of definition as we get older.

Microcurrent facial toning machines sends safe, painless impulses to the muscles in your face that help overly-tightened muscles to relax and helps under worked muscles to regain strength. In essence, microcurrent facial toning “re-educates” the facial muscles and restores them back almost to their original shape.

When this happens the visible results are quite dramatic and the face is lifted, firmed and toned back to a much more youthful appearance. At the same time, the microcurrents improve circulation to your face which stimulates production of collagen, improves tone and texture, and improves or eliminates fine lines.

Besides the fact that it really works, one of the things that makes microcurrent facial toning so popular is that most people see visible results after just a single treatment. This gives “instant gratification” which is seen so rarely as a result of other anti-aging products or techniques. In fact, the results are so noticeable that if you only treat half your face one time you can see a visible difference between the half you treated and the half you didn’t.

Microcurrent facial toning is cumulative as well, which means that the more treatments you have, the more improvement you will see in your face. The treatments are rather expensive, at an average cost of $110/treatment. Most people get at least 7-12 treatments to get their desired results.

Although microcurrent facial toning is the current “buzzword” in anti-aging, the technology is not new. It has over 50 years of historical data and clinical trials that back up its anti-aging benefits. That’s great piece of mind that shows not only will it work, but also that it is safe and does not have long term side effects.

Microcurrent facial toning is a great alternative to getting a face lift since it is non-invasive, does not require any recovery time, gives instant results, and does not have the same potential for harmful complications as surgery does.

by: Beth Larson

Anti aging center uses Microcurrent to treat aging skin

Baby boomers concerned about those inevitable lines and wrinkles that come with age now have another local treatment option.

Sharon Hladik, a licensed esthetician, has opened The Anti-Aging Skin Clinique at 40 Woodstock Avenue.

Unlike Botox treatments that require needle injections, Hladik offers non-invasive, alternative treatments to help reduce signs of aging.

Hladik uses various natural methods for body cleansing or detoxification, which includes the removal of stored toxic products from the blood, bowel, liver, kidneys and a significant amount stored in body fat.

The non-evasive treatment starts with what’s called micro-current therapy. Hladik said it’s a natural treatment that involves the delivery of micro current to the face and body using conducting wands that are applied to acupuncture points.

She said the method eliminates toxins in the skin, helping to speed cellular metabolism and increase the body chemical that fuels cells by as much as 500 percent and reconstituting the two major proteins in the skin, collagen and elastin.

Hladik said that her treatment is especially desirable for people who want to avoid the evasive procedure that accompanies Botox treatments. But unlike botox, she said her micro-current treatment isn’t a quick fix. “It’s just that it takes longer over time but is safe and effective,” said Hladik, a graduate of the Artistic Academy of Hair & Aesthetics in Morris Plains, N.J.

She said her clients typically undergo 10 to 15 weekly sessions. That’s followed by booster sessions every six to eight weeks.

Clients also have to do their part through diet and exercise, she said.

Hladik said most of her clients are part of the baby boom generation, those born between 1946 and 1964.

“Men and women are concerned about their looks,” she said. “We live in a very vain world.”

The Anti-Aging Skin Clinque offers a foot cleanse with micro-current ionic stimulation. It’s a half-hour foot bath that helps release toxins from the body. Hladik also provides nutritional assessments, facials, body waxing, eyelash and brow tinting, massage and reflexology.

Fat burning Microcurrent used in weight loss

With the holidays quickly approaching, some of us may be thinking of ways to look great for social gatherings that may come up.  For women there’s Spanks, Shape FX and many other body contouring items to help us look great in our clothing.

Unfortunately there’s nothing really for men.  But that can possibly change. 

This 26-year-old juggles being a wife, mom, and full-time college student.  On the brink of a new career, she’s taking on an attempt at a new body transformation.

“I’ve considered plastic surgery in the past but didn’t know when I could ever have it done.”

But what she’s on the verge of trying is different.  You see the Transformation Clinic claims to melt away your fat anywhere on your body, from the knees up.  It requires no downtime due to the use of micro-current technology.

How does it work?

Don Shanklin of the Transformation Clinic said, “The first part of the procedure is to liquefy the fat and the contents go thru a cell wall of the body.  Then you excrete it through the natural process.”

The second part of the session tones muscle.  And after one hour doctors say it’s almost like you just left the gym.

“You’ll have done the equivalent of 1000 sit ups.”

What about pain and discomfort?  It varies among the sexes.

“He didn’t like the first part.  I think with women being the ones to bear the babies we can take the pain,” said specialist Linda Shanklin.

“It wasn’t painful,” said this male client.

And after nine sessions of body contouring the results, “Girlfriend, you have lost 17 and a half inches.  Oh my gosh.”

The client lost eight inches off her upper waist, nine around her waist and a half of an inch around her lower.

“I’m very happy with it.  I don’t have the rectangle body.  I have an hour glass.  I can tell there is a major difference.”

She did reshape her body, but only lost five pounds.  What’s more important?  You decide.

Source:cbs42.com