The invention relates to an electrical stimulation device including a stimulator containing a generator for generating electrical stimulation pulses with defined stimulation parameters and a voltage supply for supplying the generator with electrical energy, and at least two needle electrodes for insertion into the skin surface of an area to be stimulated, which needle electrodes are connected to the stimulator.
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The electrical stimulation device in question is, in particular, applicable in the electrical acupuncture therapy of humans and even animals. The device is, in particular, suitable for using the electrical stimulation of acupuncture points in the region of the ear. Applications range from pain management to wound healing, to therapies of circulatory disorders, e.g. in diabetics.
An electrical stimulation device of the present type is, for instance, known from AT 395 106 B and EP 1 335 774 B1. There, the stimulator is glued to the skin surface by a pressure-sensitive adhesive in the vicinity of the area to be stimulated, and the needle electrodes, which are fixedly connected to the stimulator, are placed on the desired points. Also the needle electrodes can be fixed to the skin surface by appropriate adhesive elements. Especially during extended treatment periods, the stimulator or the needle electrodes may frequently detach, thus interrupting the electrical stimulation. It is, in particular, generally not possible to successfully fix the stimulator, which is larger and heavier than the needle electrodes, to the skin surface of a patient over extended periods of up to several days.
The aim of the present invention is to provide an above-identified electrical stimulation device that avoids the drawbacks of known stimulation devices and allows for simple and quick application and safe stimulation even over several days. The device is to be producible as simply and cost-effectively as possible so as to even enable its economical application as a disposable product.
The object of the invention is achieved in that the needle electrodes are arranged in a common electrode housing and connected to the stimulator via a line. In accordance with the invention, the mass electrode and the at least one stimulation electrode are thus arranged in a common electrode housing, which facilitates and accelerates its application, i.e. insertion into the skin surface, yet also improve the adherence to the skin surface or attachment to the skin surface. As a function of the respective application, at least one mass electrode and at least one stimulation electrode are arranged in the electrode housing. The needle electrodes are likewise adapted to the respective application, yet also to the patient undergoing treatment, or the animal undergoing treatment. For an electrical acupuncture in the region of the ear of a human being, the needle electrodes have diameters of a few tenths of millimeters and insertion depths of few millimeters. In order to achieve a length compensation and an increase in the mobility of a patient, it may be advantageous to configure the line as a coiled cable.
In order to be able to achieve the detachment of the needle electrodes from the stimulator and, for instance, take off the stimulator during showering, it is advantageous if the line is provided with at least one plug for the detachable connection to a respective socket provided on the stimulator or on the electrode housing. This will enable the patient or a nursing attendant to simply separate the electrode housing from the stimulator and reconnect it thereto. The line can be fixedly connected to the electrode housing, and the plug can be fastened to the end of the line, and the stimulator can be equipped with an appropriate socket. It is also possible to fixedly connect the line to the stimulator, and to arrange the plug on the end of the line and the associated socket on the electrode housing.
In an advantageous manner, the needle electrodes are arranged on a common board within the electrode housing. A suitable board will thus comprise a number of openings that corresponds to the number of needle electrodes, for inserting the needle electrodes, and conductive tracks that are connected to connecting points for the line, for connecting to the stimulator or a respective socket in the electrode housing.
In an advantageous manner, the needle electrodes are connected to the board by a conductive adhesive. This will enable rapid and cost-effective production.
The line can be connected to the board by a solder or screw connection. Solder connections are particularly advantageous with especially small-structured electrode housings.
The needle electrodes are made of an electrically conductive material, in particular a metal such as titanium, stainless steel or the like. The insertion electrodes can be produced by lathing. In addition to metals, conductive synthetics are also conceivable for the production of the needle electrodes, the materials having to exhibit the respective biocompatibility and avoid allergic reactions.
The electrode housing is advantageously designed to be water-proof, which will enable the temporary separation of the electrode housing from the stimulator, and hence the patient to even take, for instance, a shower.
In order to improve the fixation of the electrode housing to the skin surface, a fastening element, preferably an adhesive element, may be provided. Besides the adhesive element, other fastening methods, e.g. via elastic bands or the like, are conceivable as a function of the location of stimulation and the patient or animal, respectively.
The fastening element, which is preferably designed as an adhesive element, can already be integrated in the electrode housing. This will further facilitate its application, since the patient or the physician does not need to position the fastening element on the electrode housing, but merely needs to pull off, for instance, a cover foil from an adhesive layer.
On the side of the electrode housing opposite the needle electrodes, a handling element may be arranged to facilitate the application of the electrode housing, and the needle electrodes disposed therein, on the desired site, e.g. on the ear.
Such a handling element can be formed by a substantially cylindrical handle, which is preferably produced in one piece with the electrode housing. Such a handling element can be very simply produced by injection molding, in particular with usual electrode housings made of synthetic material.
The handling element can also be formed by a depression or hole in the electrode housing, in which a respectively designed counter-piece of a handling instrument can be arranged. In this respect, cylindrical, spherical or conical depressions are, for instance, applied.
Since the needle electrodes are inserted into the skin surface, it will be advantageous if the electrode housing with the needle electrodes contained therein is arranged in a package, optionally together with the line fastened to the electrode housing. Contamination will thus be avoided. The components are preferably sterilized before or after packaging.
In order to achieve an elevated wearing comfort of the stimulation device, the stimulator can be coupled to a lanyard, which can be worn around the neck like a halter neck, or over the shoulder. The lanyard can at least partially be configured as a line for connecting to the electrode housing and provided with a socket or a plug for connecting to the line attached to the electrode housing. Other options for fastening the stimulator, for instance by the aid of fastening elements in the form of ear clips, can also be envisaged.
The generator of the stimulator is preferably configured to generate stimulation pulses having a repetition frequency of 0.5 to 100 Hz, preferably 1 Hz, and a duty cycle of 10 to 90%, preferably 50%. These stimulation parameters have turned out to be preferred in pain therapy or wound healing.
Since the impedance of the skin comprises large variations, it will be advantageous if the stimulation pulses are generated at a constant current amplitude. To this end, the stimulator comprises an appropriate control device. The control device may be comprised of a suitable microcontroller.
Where the control device is coupled to operating elements for changing the stimulation parameters, manual adjustment and change of the stimulation parameters may be provided. Where no operating elements are provided, the respective adjustment of the stimulation parameters can be performed by programming the control device. To this end, the stimulator preferably comprises a suitable interface for connecting to a control computer.
A switch or the like can be provided to activate the stimulator. Alternatively, the activation can, for instance, also be realized by removing an insulator on the battery constituting the voltage supply.
In order to give a feedback on the operation of the stimulation device to the patient or the physician, an operation indicator, e.g. a light-emitting diode, can be provided in the stimulator. In addition to an optical operation indicator, an acoustic indicator of the proper operation or proper start-up can also be provided.
Advantageously, a memory for recording the stimulation parameters as a function of time is provided to enable the performance of a quality control check or check of the proper operation.
The present invention also relates to an above-identified electrode housing including at least two needle electrodes with optional lines to connect to the stimulator. Such an electrode housing can also be marketed separately, unless the stimulator is sold together with the electrode and designed as a disposable product. If the stimulation device is designed as a disposable product, the stimulator is packed together with the electrode housing and the needle electrodes arranged therein, whereby, in particular, the needle electrodes will be protected from contamination, e.g. by a separately provided blister package.
The present invention will be explained in more detail by way of the accompanying drawings. Therein:
As is apparent from the sectional illustration according to
Furthermore, an appropriate clock generator 20, which may, for instance, be formed by a quartz crystal, is coupled to the control device 15. If the stimulator 2 comprises a memory 21, the stimulation parameters can be recorded as a function of time for subsequent examinations or for quality control. The memory 21 can be read out by an appropriate computer via the interface 16.
To indicate the proper functioning of the stimulation device 1 and the stimulator 2, respectively, an appropriate operation indicator 22 can be provided, which may, for instance, be formed by a light-emitting diode.
As already described in
Number | Date | Country | Kind |
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GM 414/2010 | Jun 2010 | AT | national |
This application is the National Stage of International Application No. PCT/AT2011/000218, filed on 9 May 2011 claiming the priority of AT GM 414/2010, filed on 30 Jun. 2010, the content of each of which is incorporated by reference herein.
Filing Document | Filing Date | Country | Kind | 371c Date |
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PCT/AT11/00218 | 5/9/2011 | WO | 00 | 2/26/2013 |