MEDICAL TREATMENT DEVICE AND METHOD OF OPERATION THEREOF

Abstract

There is disclosed a system for providing transcutaneous electrical stimulation to the vagus nerve of an individual comprising: an electrode unit mountable within the auricle of the individual and having at least a first electrode and a second electrode for applying the transcutaneous electrical stimulation at the cymba conchae and the tragus of the individual's auricle, and a controller for controlling the transcutaneous electrical impulse delivered by each of the first electrode and second electrode.

Claims

1. A system for providing transcutaneous electrical stimulation to the vagus nerve of an individual comprising: an electrode unit mountable within the auricle of the individual and having at least a first electrode and a second electrode for applying the transcutaneous electrical stimulation at the cymba conchae and the tragus of the individual's auricle; a controller for controlling the transcutaneous electrical impulse delivered by each of the first electrode and second electrode.

2. A system according to claim 1, wherein the transcutaneous electrical stimulation is applied to the auricular branch of the vagus nerve of the ear.

3. A system according to claim 2, wherein the electrical stimulation includes transmission of the electrical impulse applied to the auricular branch of the vagus nerve of the ear to central brain projections

4. A system according to claim 1, wherein the waveform of the electrical stimulation supplied by the controller is asymmetric.

5. A system according to claim 2, wherein the waveform of the electrical stimulation supplied by the controller is biphasic.

6. A system according to claim 5, wherein the waveform of the electrical stimulation supplied by the controller is sinusoidal.

7. A system according to claim 1, wherein the controller is able to control the pulse rate of the electrical stimulation applied by the electrodes.

8. A system according to claim 7, wherein the controller is able to control the pulse width of the electrical stimulation applied by the electrodes.

9. A system according to claim 1, wherein the controller is able to control the pulse amplitude of the electrical stimulation.

10. A system according to claim 1, wherein the electrode unit comprises a moulded body configured to be mounted within the auricle of the individual

11. A system according to claim 10, wherein the first electrode and the second electrode are mounted within the moulded body.

12. A system according to claim 10, wherein each of the first electrode and second electrode are mounted within a housing that is movably mounted to the moulded body to facilitate adjustment of the position of the first and second electrodes with respect to the vagus nerve.

13. A system according to claim 11, wherein the moulded body is made of a semi-flexible material.

14. A system according to claim 12, wherein the moulded body is formed in a variety of different sizes to accommodate different sized auricles.

15. A system according to claim 10, wherein the molded body is made of a material including silicone.

16. A system according to claim 10, wherein the moulded body includes a first and a second recess for receiving the first and second electrode respectively.

17. A system according to claim 10, wherein the moulded body has at least one projecting portion for projecting into the ear of the individual to aid in retaining the electrode unit in position.

18. A system according to claim 15, wherein the at least one projecting portion projects into the ear canal of the ear of the individual.

19. A method of stimulating the auricular branch of the vagus nerve of an individual for treatment of a medical condition comprising: positioning a first stimulator adjacent a cymba conchae of the individual; positioning a second stimulator adjacent an inner surface of a tragus of the individual; applying electrical stimulation between the first and the second stimulators at a predetermined frequency and pulse duration for a predetermined period.

20. A method according to claim 19, wherein the electrical stimulation is applied between the first and second stimulators at a frequency of 25 Hz, pulse duration of 500 μs with an alternating cycle for a period of 10 minutes.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

[0028] The invention may be better understood from the following non-limiting description of preferred embodiments, in which:

[0029] FIG. 1 is a view of an auricle of a user suitable for using the present invention;

[0030] FIG. 2 is a view of the auricle of FIG. 1 with an electrode unit in accordance with an embodiment of the present invention in position;

[0031] FIG. 3 is a view of a system for providing transcutaneous electrical stimulation to the vagus nerve in accordance with an embodiment of the present invention;

[0032] FIG. 4 is a perspective view of an embodiment of an electrode unit in accordance with the present invention; and

[0033] FIG. 5 is a different perspective view of the top view of the electrode unit depicted in FIG. 4.

DETAILED DESCRIPTION OF THE DRAWINGS

[0034] Preferred features of the present invention will now be described with particular reference to the accompanying drawings. However, it is to be understood that the features illustrated in and described with reference to the drawings are not to be construed as limiting on the scope of the invention.

[0035] The system and method of the present invention will be described below in relation to a non-invasive device for applying therapeutic stimulation of the vagus nerve via the external ear. However, it will be appreciated that the system and method of the present invention could also be achieved by applying stimulation to the vagus nerve at other sites, using either an invasive or minimally invasive stimulation system.

[0036] The present invention is primarily directed towards addressing inflammation issues in the human body. It is based on an understanding that communication between the immune system and the brain is vital for controlling inflammation. The inflammatory reflex is a centrally integrated physiological mechanism in which afferent vagus nerve signalling, activated by cytokines or pathogen-derived products, is functionally associated with efferent vagus nerve-mediated output to regulate pro-inflammatory cytokine production and inflammation. The present invention utilises this physiological reflex and system and stimulates the regions of the brain responsible for this reflex, actively regulating pro-inflammatory cytokines.

[0037] Referring to FIG. 1, an auricle or external ear 10 of a human is depicted for use with the present invention. The vagus nerve is one of the cranial nerves that connects the brain to the body and can be generally thought of as a circuit that links the neck, heart, lungs and abdomen to the brain. Whilst located internally, the vagus nerve has an auricular branch that supplies afferent sensory innervation from the auricle 10, ear canal 12 and tragus 14. In this regard, the auricular branch of the vagus nerve is distributed to the skin at the back of the auricle and to the posterior part of the ear canal as is shown in FIG. 1. This results in the distribution of the Auricular Branch of the Vagus Nerve (ABVN) to the cymba conchae, and a portion of the area surrounding the auditory meatus, including the inner/antero-medial aspect of the tragus. For the purposes of the present invention reference is also made to the cymba conchae 16 which also provides direct access to the auricular branch of the vagus nerve.

[0038] In accordance with the present invention, in order to best access the vagus nerve, it is considered ideal to apply electrical stimulation to the surface of the auricle adjacent the cymba conchae 16 and the inner surface of the tragus 14, as depicted in FIG. 1. To achieve this, an electrode unit 20 of FIG. 2 is provided.

[0039] The electrode unit 20 is in the form of a silicone body 25 adapted to be worn in the external ear 10 of the individual. The silicone body 25 is a mouldable body that is configured to fit within the outer ear of the user in a manner that automatically aligns incorporated electrodes 22, 24 with the tragus 14 and cymba conchae 16 respectively, when the electrode unit 20 is worn. As will be discussed in more detail below, the body 25 has a portion that is adapted to be received within the ear canal 12 of the wearer so as to be retained in position during use in a comfortable and effective manner. In this regard, the body 25 of the electrode unit 20 may be moulded to conform with the outer ear of the user or may be formed in a generic manner with sufficient variability to be used by any individual so as to be effectively and comfortable worn with minimal adaptation.

[0040] The electrodes 22 and 24 are in the form of discrete electrode discs positioned at the surface of the body 25 such that when the electrode unit 20 is positioned for use, the electrodes 22, 24 are in contact with the skin surface at the tragus 14 and the cymba conchae 16 for delivery of the stimulation regime to the vagus nerve. Each electrode 22, 24 has a wire 26 connected thereto which extends from a cord 27 to a remotely located stimulator unit 28 which controls and regulates the stimulation applied by the electrodes 22, 24, as shown in FIG. 3. The wires 26 are embedded within the body 25 by way of dedicated tunnels formed therein, as will be described in more detail below.

[0041] Alternatively, the electrodes 22, 24 may comprise a transmitter/receiver unit (not shown) to wirelessly connect with a stimulator unit 28 to receive and process the control signals received by the stimulator unit 28 for application. In such an embodiment, the transmitter/receiver unit may also be embedded within the body adjacent the electrodes 22, 24.

[0042] In another embodiment, each of the electrodes 22, 24 may be mounted within a housing that is pivotally attached to the body 25 to enable a degree of adjustment by the wearer to correctly position the electrodes 22, 24 at the desired stimulation site. The electrodes 22, 24 may be mounted to an extremity of the housing so as to be positioned directly against the wearer's skin.

[0043] The stimulator unit 28 may be in the form of a conventional TENS/EMS control unit that is capable of controlling the frequency and amplitude of the stimulation applied by each electrode 22, 24 and may be programmed or adjusted according to the individual user's requirements.

[0044] Referring to FIGS. 4 and 5, alternative views of the electrode unit 20 are shown detailing the manner in which the electrode discs are positioned for use. As is shown, the body 25 is moulded from a silicone or similar material to have recesses 22a, 24a formed at the appropriate locations to receive and hold the electrodes for use. A projection 30 is formed on the body 25 to be located at least partially within the ear canal 12 of the user to locate and orientate the body 25 in position. When in this position, the electrodes 22, 24 are positioned immediately in contact with the surface of the user's ear adjacent the tragus 14 and cymba concha 16 respectively. This enables the electrical stimulation to be delivered from the electrode surface and to the vagus nerve. Tunnels or channels 32 are formed within the body 25 to accommodate the leads 26 connecting the electrodes 22, 24. The leads 26 each exit the body 25 at a substantially common point to ensure that the unit 20 is comfortably secured in position for use.

[0045] It will be appreciated that the body 25 whilst having a common configuration, will be supplied in a variety of sizes to accommodate different sized ears and different ages of users. In such instances, the electrode positions 22, 24 will be the same within the body 25, but the body 25 will be sized differently. It will be appreciated that given the nature of the material used and the shape of the body 25, once it has been appropriately positioned within the user's ear it will be maintained in position due to the fitted interaction of the unit 20 with the user's ear.

[0046] The system of the present invention is primarily directed towards providing concentrated vagus nerve stimulation for the treatment of those suffering from inflammation type conditions, including, but not limited to, headache/migraine and inflammatory autoimmune conditions, or any other condition impacted by a disruption of the normal vagus nerve tone, including such conditions as recurrent laryngeal paralysis, traumatic brain injury, mood disorders, and nausea.

[0047] The remote controller will be body worn or carried by the user and will be programmable to deliver a biphasic asymmetric sinusoidal stimulation signal via the duel electrodes of the electrode unit 20 to the auricular branch of the vagus nerve. The controller may be configured to enable the user the ability to vary the stimulation pattern being applied but to prevent the user from altering the stimulation pattern beyond their predetermined conditions pre-set for the user. This may prevent the user from altering the waveform of the stimulus to ensure that the stimulation being applied is within acceptable limits. The controller may control the pulse rate of the stimulation and the pulse width of the stimulation.

[0048] The preferred pulse rate of the stimulation applied by the system may be around 25 Hz, with a range of between 1-200 Hz. The pulse width of the stimulation may be around 500 μs with a range varying from between about 10 μs-500 μs. It has been found that the wider the pulse rate the more preferable the body response, as the body seems to habituate at smaller pulse widths. It is difficult to maintain pulse widths greater than 500 μs, and it has been found that a pulse rate of between 400-500 μs is the “sweet spot” for activation. Similarly, the pulse amplitude should be around 0-90 mA and usually under 10 mA. An example of an optimized stimulation regime program for a patient may include applying stimulation between the stimulation sites at a frequency of 25 Hz, pulse duration of 500 μs with an alternating cycle for a period of 10 minutes.

[0049] The stimulation may be applied by the electrodes 22, 24 simultaneously to the different regions of the auricular branch of the vagus nerve. Alternatively, the stimulation may be applied sequentially by the electrodes 22, 24, or in a predetermined pattern. By targeting both the cymba conchae and the inner portion of the tragus, more targeted stimulation is achievable as the auricular branch of the vagus nerve (ABVN) supplies both of these structures.

[0050] The controller will preferably be portable and will be powered by a rechargeable or replaceable 9V power pack or battery. The duration of use may vary from user to user and will largely be dependent on the guidelines provided with the device. In another embodiment, the controller may by a dedicated software application uploaded to the user's smart phone. The user may control the electrode unit 20 by controls provided within the software application which can be regularly updated as required.

[0051] It will be appreciated that the present invention provides a system and apparatus for providing a targeted stimulation of the vagus nerve to address a number of well-established conditions. Through the use of both the cymba conchae and the inner portion of the tragus as a stimulation site, more targeted stimulation is achievable as the auricular branch of the vagus nerve (ABVN) supplies both of these structures. By targeting these locations and performing targeted stimulation between these sites, a wider range of conductivity is able to be utilized to ensure optimal stimulation.

[0052] The present invention has been found to facilitate decreases in the activity of second-order nociceptive neurons in the spinothalamic and spinoreticular tracts of the spinal cord, as well as in the trigeminal nuclear complex. Central brain projections also have a significant effect on modulating sympathetic and parasympathetic activity (or vagal tone, which when higher, is associated with an increased heart rate variability), reducing oxidative stress and stimulating the release of neurotransmitters including norepinephrine and serotonin.

[0053] Throughout the specification and claims the word “comprise” and its derivatives are intended to have an inclusive rather than exclusive meaning unless the contrary is expressly stated or the context requires otherwise. That is, the word “comprise” and its derivatives will be taken to indicate the inclusion of not only the listed components, steps or features that it directly references, but also other components, steps or features not specifically listed, unless the contrary is expressly stated or the context requires otherwise.

[0054] It will be appreciated by those skilled in the art that many modifications and variations may be made to the methods of the invention described herein without departing from the spirit and scope of the invention.