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Contributors: GTL, JNK, and STH conceived the study, developed the protocol, and obtained funding. JB was the trial manager. JG was responsible for the statistical design and randomisation, and PP for the analysis. All authors were jointly involved in writing the paper. STH will act as guarantor.
To evaluate whether electrodermal testing for environmental allergies can distinguish between volunteers who had previously reacted positively on skin prick tests for allergy to house dust mite or cat dander and volunteers who had reacted negatively to both allergens.
Double blind, randomised block design.
A general practice in southern England.
15 volunteers who had a positive result and 15 volunteers who had a negative result on a previous skin prick test for allergy to house dust mite or cat dander.
Each participant was tested with 6 items by each of 3 operators of the Vegatest electrodermal testing device in 3 separate sessions (a total of 54 tests per participant). For each participant the 54 items comprised 18 samples each of house dust mite, cat dander, and distilled water, though these were randomly allocated among the operators in each session. A research nurse sat with the participant and operator in all sessions to ensure blinding and adherence to the protocol and to record the outcome of each test.
The presence or absence of an allergy according to the standard protocol for electrodermal testing.
All the non-atopic participants completed all 3 testing sessions (810 individual tests); 774 (95.5%) of the individual tests conducted on the atopic participants complied with the testing protocol. The results of the electrodermal tests did not correlate with those of the skin prick tests. Electrodermal testing could not distinguish between atopic and non-atopic participants. No operator of the Vegatest device was better than any other, and no single participant's atopic status was consistently correctly diagnosed.
Electrodermal testing cannot be used to diagnose environmental allergies.
Unconventional allergy tests such as electrodermal testing are used widely in complementary and alternative medicine. We wanted to compare the reliability of one common method of electrodermal testing for IgE dependent allergy, the Vegatest, with that of the gold standard for evaluating allergies, skin prick testing. The protocol for the Vegatest has been outlined elsewhere.1
Electrodermal testing was developed as an aid in prescribing homoeopathic remedies1 but is now widely used to assess an individual's allergic status to foods and aeroallergens. It is based on the observation that small changes in electrical impedance in the skin occur on an acupuncture point in response to substances placed in an electrical circuit (fig (fig1).1).
We estimate that more than 500 electrodermal devices are currently being used in the United Kingdom to assess sensitivity to potential allergens (see BMJ 's website for further details). We have no reliable information on the use of electrodermal testing in other countries or the extent to which it is used to detect food allergens rather than aeroallergens. Electrodermal testing for allergic and intolerance responses to dietary and environmental allergens—for which there are several different devices—has become increasingly popular, possibly because of its safety, non-invasive nature, and simplicity; therefore rigorous evaluation of electrodermal testing is important. The suggested mechanisms range from pressure changes over the acupuncture point that are produced unconsciously by the examiner to more objective mechanisms that are independent of the operator and are summarised as “quantum biology.”2,3
There have been several scientifically inadequate studies of electrodermal testing as a potential means of evaluating “allergy.”4–9 Because the evidence base for using electrodermal testing to diagnose IgE dependent allergy is limited in quality and size, we undertook a clinical trial to test the hypothesis that electrodermal testing distinguishes between individuals who are sensitised to aeroallergens, as determined by skin prick tests, and non-atopic people.
The study was carried out at a general practice, the Hythe Medical Centre, in Southampton. The volunteers were recruited through advertisements and from a departmental database. Volunteers were entered if they were aged between 18 and 65 but were excluded if they had any uncontrolled systemic disease, had taken part in any drug trial in the previous 30 days, had taken oral corticosteroids in the previous month or H1 antihistamines one week before electrodermal testing, or were pregnant. Those who reacted positively to a skin prick test for allergy to house dust mite or cat dander were entered as atopic. The skin prick test compares the effects of the test substance and a negative control when the skin is pricked through a drop of each substance. We defined a positive result as a wheal that 10 minutes after the puncture was 3 mm greater in diameter than that made by the control substance. The first 15 eligible volunteers were entered into each of the atopic and non-atopic groups. Skin prick testing, a method of evaluating allergic status that is reproducible and remains stable over a four month period,10,11 was carried out under a standard protocol12 between 2 and 16 weeks before the electrodermal testing sessions. Ethical approval was obtained from the Southampton and south west Hampshire joint research ethics committee.
The operators were experienced electrodermal testers, each having used this procedure in a clinical setting for over 10 years. The four operators provided their own Vegatest machines (Vega Medizinische Geräte, Schiltach, Germany). The machines were set up in the standard manner for evaluating allergic responses,1 with four ampoules of homoeopathic epiphysis D26 and one ampoule of homoeopathic histamine D60 in the testing honeycomb (figure (figure1).1). The individual to be tested held a hand electrode, and the “Vega probe” was placed on the terminal acupuncture point on the lateral aspect of the third toe (the spleen/pancreas meridian).1 In each test the operator measured the skin impedance at this point as indicated in arbitrary units on the galvanometer while the patient held the hand electrode to complete the electrical circuit. Each time a new glass ampoule containing the experimental substance was placed in the Vegatest honeycomb, the operator again measured the skin impedance.
At the beginning of each testing session, each operator adjusted the baseline recording on the galvanometer so that the scale registered 100 units. The operator then placed an ampoule containing a toxic substance (the disorder control), such as mercury or paraquat, into the honeycomb in accordance with the standard Vegatest protocol.1 If the galvanometer reading was 60-70 units, the participant was diagnosed as “allergic,” and the operator instructed the research assistant to note that the individual being tested was sensitive to the substance within the ampoule. If the galvanometer read 100 units, the classification “not allergic” was recorded. The magnitude of the readings is not considered to be proportional to the extent of allergic sensitisation. If the operator was unable to define the individual's allergic status on more than two ampoules tested at any testing session, that person's data were not included in the analysis.
The measured outcome was the operator's assessment of the presence or absence of “allergy” for each of the ampoules tested on each individual participant. From previous reports,7–9 we expected that the sensitivity of the Vegatest would be about 0.7 and the false positive rate 0.15, with little variation among participants. Assigning 12 people to each of the two groups would achieve a statistical power of 90% (a two sided normal test at a 5% level of significance) even if the variance among participants was as high as 0.14. Thus, to compensate for dropout we recruited 15 volunteers to each group. The statistician (PP) processed the data before breaking the randomisation codes.
A pool of four operators performed the electrodermal tests over three fixed dates and a fourth flexible date for those who had difficulty attending one of the prebooked sessions. On each day three of the four operators attended the sessions at the clinic. At each session the participants were tested by each operator for their allergic reaction to six ampoules. Each participant was therefore evaluated for their response to 18 individualampoules at each visit. The contents of the test ampoules were changed for each operator on each day. Each ampoule contained only one item, either an allergen extract (house dust mite or cat dander; Bayer Dome Hollister Stier, Washington, DC) or a non-allergen (distilled water). Over all the tests in each session each participant was tested with six ampoules containing house dust mite extract, six of cat dander extract, and six of distilled water, but the contents of each individual set of six ampoules were randomised (fig (fig2).2).
The order of testing and the specific content of the ampoules was determined by random numbers generated by a computer. The order of presentation of the ampoules was randomised for each participant individually, and the order of testing was randomised in blocks of six ampoules. The sets of ampoules were made up at an independent homoeopathic dispensary (the Centre for the Study of Complementary Medicine, Southampton) with numerical codes on each of the bottles. The ampoules containing the two allergens could not be distinguished from one another or from the distilled water. To ensure complete blinding the trial manager was not present at any of the individual testing sessions. A research assistant stayed with the operators throughout each session to ensure that they did not question the participants on their medical history. The research assistant also placed each ampoule to be tested into the Vegatest honeycomb and recorded the operator's identification of the participant as either allergic or not allergic. The research assistant then returned the set of six ampoules to the trial manager at the end of each clinical session.
A total of 1596 individual tests were completed. All 15 non-atopic participants completed all the tests and complied with the testing protocol (810 tests). The atopic participants completed 786 tests, of which 774 complied with the protocol (figure (figure2).2). The percentages of “allergic” and “non-allergic” participants as determined by the operators are shown in table table1.1. Overall the operators reported a positive (allergic) response (a reading of 60-70 units of the scale) in a quarter of the tests and a negative (non-allergic) response in nearly three quarters; they were unable to assess 1.0% of the responses as either allergic or non-allergic.
The Vegatest readings from the atopic group did not differ significantly from those of the non-atopic groups. The mean percentage of Vegatest results that accorded with the results of the skin prick tests was normally distributed, and the Vegatest was unable to differentiate between atopic and non-atopic groups for each of the allergens: 24% of atopic participants versus 22% of non-atopic participants were diagnosed by the Vegatest operators as being sensitive to cat dander; 28% versus 29% to house dust mite, and 26% versus 23% to distilled water. No individual participant's allergic status as determined by skin prick testing was consistently correctly diagnosed by all the Vegatest operators.
We also analysed each operator's results for each substance tested in both groups of participants and found no significant differences from the overall patterns. The operators' overall results are shown in table table2.2. There was no difference in reliability among the operators, no significant differences in the accuracy of individual operators, and no significant positive or negative correlation between the results of the Vegatest and those of the skin prick test for any operator (data not shown). Analysis of false positive and false negative data did not show any significant differences among the operators or any significant correlation between the results of the Vegatest and those of the skin prick test.
This double blind, randomised block design study, which comprised over 1500 observations, showed that electrodermal testing could not distinguish atopic from non-atopic individuals. No operator was more reliable than any other, and no participants were consistently correctly diagnosed.
As IgE dependent food allergy—for example, to milk, eggs, or nuts—has the same pathophysiological basis as mucosal responses to aeroallergens, we conclude that the Vegatest is an inappropriate tool for diagnosing any form of immediate hypersensitivity. However, we recognise that electrodermal testing, when used to assess “antigens” in a non-blinded manner, is usually used to evaluate food intolerance rather than to diagnose allergies in the traditional sense of the term.8 We did not investigate food intolerance, partly because there is no universally recognised conventional test for food intolerance against which to evaluate electrodermal testing. Nevertheless, it should be possible to design an appropriate trial to study the diagnostic usefulness of the Vegatest for food intolerance reported by patients, although it is difficult to envisage a unifying mechanism to explain how the test would be able to detect this heterogeneous group of disorders. Furthermore, we recognise that electrodermal testing was developed to aid the prescription of homoeopathic and herbal remedies and not primarily as an allergy test; we made no attempt to evaluate these claims.1 The phenomena involved in electrodermal testing may make it difficult to evaluate in an entirely blind manner, as the person conducting the test may be an important part of the process.2,3 Such issues can be addressed by appropriate randomised, controlled trials. We conclude that electrodermal testing cannot diagnose allergy to common aeroallergens such as cat dander and house dust mite—allergens that have a strong association with atopic respiratory disorders such as asthma, rhinitis, eczema, and conjunctivitis.
Unconventional testing for allergy, such as electrodermal testing, is widely available
Few clinical trials have evaluated unconventional testing
Electrodermal testing cannot distinguish between atopic and non-atopic individuals as previously determined by skin prick tests
We thank Jackie Burnham for her help in preparing the manuscript, all the volunteers and the operators who gave up their time so willingly, and the doctors and practice manager at Hythe Medical Centre who made space and time available to us.
Funding: The study was supported by funding from Vega Grieshaber, the Asthma Allergy and Inflammation Research Trust, and the Foundation for Integrated Medicine.
Competing interests: GTL and JNK formerly had interests in a company involved in the distribution of Vega Grieshaber products and both have received fees for speaking at a seminar on the Vegatest.
Further details of electrodermal tests are available on the BMJ's website