VIBRATORY INTRA-ORAL BIOFEEDBACK APPARATUS

Abstract

A vibratory intra-oral biofeedback apparatus for the treatment of orofacial pain and temporo-mandibular dysfunction by providing a stimulus in response to involuntary or parafunctional contraction of the chewing muscles above a pre-set limit, comprising at least one active device formed by a set of functional elements, the latter comprising a vibrator, at least one sensor, batteries, and processor. Said device is sealingly inserted in a plate made of synthetic resin which in the preferred embodiments is configured according to the contour of the dental arches in which it fits. The stimulation in the form of vibration is triggered when the force of involuntary contraction of the chewing muscles reaches a threshold which generally ranges from 20 N to 70 N. The apparatus may comprise two active devices located on the left and right side of the arch or just an active device, located on one side, left or right, of the arch.

Claims

1. A vibratory intra-oral biofeedback apparatus for treating orofacial pain and temporo-mandibular dysfunction by providing a stimulus in response to involuntary or parafunctional contraction of the chewing muscles above a pre-set threshold, consisting of an autonomous apparatus containing at least an active device composed of a set of functional elements comprising at least one vibrator, at least one sensor, at least one battery and a processor, said set of functional elements being sealingly inserted in a synthetic resin mouth guard, wherein said pre-set threshold is adjustable between the values of 20 N and 70 N and in that it comprises two modes of installation in the oral cavity of the patient, the first consisting of the installation by the dentist at the dentist's office and the second consisting in the installation performed by the patient.

2. An apparatus as claimed in claim 1, wherein it comprises a unit located at the frontal portion of the dental arch, said active device being embedded in said unit.

3. An apparatus as claimed in claim 1, wherein the adjustment of said threshold is performed during the manufacture of the apparatus.

4. An apparatus as claimed in claim 1, wherein the adjustment of said threshold is performed in the dental office by the dentist.

5. An apparatus as claimed in claim 1, wherein it comprises two mouth guards respectively fitted in the upper and lower dental arches, one of which contains, sealingly inserted therein, at least such an active device.

6. An apparatus as claimed in claim 5, wherein the lower mouth guard includes said active device which comprises at least one vibrator at least one sensor, at least on battery and a processor, said at least one sensor being selected from the group comprising mechanical switches, strain gages, load cells, conductive rubber or piezoelectric sensors.

7. An apparatus as claimed in claim 5, wherein the upper mouth guard includes said active device which comprises at least one vibrator at least one sensor, at least on battery and a processor, said at least one sensor being selected from the group comprising mechanical switches, strain gages, load cells, conductive rubber or piezoelectric sensors.

8. An apparatus as claimed in claim 6, wherein the top mouth guard comprises at least one protrusion, positioned coincidentally and in opposition to said at least one sensor.

9. An apparatus as claimed in claim 7, wherein the lower mouth guard comprises at least one protrusion, positioned coincidentally and in opposition to said at least one sensor.

10. An apparatus as claimed in claim 1, wherein it comprises two active devices located, one on the left side and one on the right side of the dental arch.

11. An apparatus as claimed in claim 1, wherein it comprises a single active device located either on the left or on the right side of the dental arch.

12. An apparatus according to claim 1, wherein the adjustment of said threshold is provided by digitally encoded signals, transferred between an external programming unit and said active device by proximity inductive coupling of a first coil located in said programming unit and a second coil installed in the mouth guard containing the active device.

13. An apparatus according to claim 1, wherein the active device is embedded in a thermo-activated synthetic resin.

Description

DESCRIPTION OF THE FIGURES

[0032] Further advantages and features of the invention will become more apparent from the description of preferred exemplary embodiments and corresponding figures, given as non-limiting examples, wherein:

[0033] FIGS. 1, 2 and 3 show previous art devices for treating bruxism.

[0034] FIGS. 4-a and 4-b show a first embodiment of the device, according to the principles of the present invention.

[0035] FIGS. 5-a, 5-b and 5-c show a second embodiment of the device, according to the principles of the present invention.

[0036] FIGS. 6-a, 6-b and 6-c show a third embodiment of the device, according to the principles of the present invention.

[0037] FIG. 7 shows a detailed view of the device placement on the dental arch.

[0038] FIG. 8 shows a fourth embodiment of the device, according to the principles of the present invention.

DETAILED DESCRIPTION OF THE INVENTION

[0039] By filling in the gaps of the existing options, the poposed device, which is based on an innovative principle, elicits a quite favorable reaction on the part of the patient.

[0040] As mentioned, nocturnal involuntary muscle contraction is usually responsible for morning headaches, migraine aggravation, TMJ overload and lesions, facial pain, tooth sensitivity, and finally, overload off the masticatory system comprising muscles, joints, nerves and blood vessels.

[0041] Firstly, the device of the invention reduces the strength of muscle contraction, also reducing joint compression and arterial and venous overload in the region. Such a reduction has an analgesic and myo-relaxing effect and even an anti-inflammatory effect from the mechanical point of view. After the symptoms subside, the constant or eventual use of the device can prevent the return of symptoms, being an effective substitute for physiotherapy and even psychotherapy, as it teaches the patient good postural mouth customs. By preventing the problem from getting worse, it can avoid the need for future surgery.

[0042] According to FIGS. 4-a and 4-b, the apparatus comprises an upper mouth guard 11 and a lower mouth guard 12, made of synthetic resin, respectively fitted in the upper and lower dental arches 13 and 14. In the embodiment shown, the lower mouth guard is provided with an active device comprising the sensors 15, which may comprise mechanical switches, strain gages, load cells, conductive rubber or piezoelectric sensors. Said active device also comprises a microprocessor (not shown), batteries 17 and at least one vibrating element 18 of a known type, connected to each other and to said sensors.

[0043] The upper mouth guard 11 is passive and comprises a set of protrusions 16, positioned coincidentally and in opposition to said sensors 15, so that, upon occlusion, as exemplified in FIG. 4-b, said protrusions press the sensors which produce an electrical signal whose intensity is proportional to the biting force. Said signal is analyzed by the microprocessor; if such magnitude indicates a biting force above a preset threshold, a vibrator 18 is triggered. This embodiment of the invention employs the vibratory action to treat snoring and apnea associated with protrusion of the mandible, in order to result in muscle relaxation at the same time.

[0044] These vibrations or buzzing are perceived consciously or unconsciously by the patient, causing the reflex arc mechanism to interrupt the muscle contraction. Vibration will be triggered every time the biting force exceeds the preset limit, inducing a reduction of muscle contraction during the period in which the apparatus is used. The threshold value of the biting force between the opposing teeth which results in actuation of the apparatus can generally be set between 20 N and 70 N, with 40 N being the default value. Such a threshold can be pre-programmed during manufacturing, depending on the characteristics of the user, evaluated by the health professional. In another embodiment of the invention, the adjustment may be performed in the dentist's office.

[0045] The material used in the manufacturing of the mouth guards is preferably a synthetic resin comprising plastics of various types (polyurethanes, polycarboxylates, PET, silicone, and so on) which, in addition to providing electrical insulation between the elements, provides the watertight sealing of the assembly, a feature that is necessary in view of the conditions found in the oral cavity.

[0046] Of course, the functions of the said mouth guards can be reversed, with the active device, containing the electronic components, installed in the upper component, and the passive elements, i.e. the pressing projections 16 being provided in the lower component. Said reversal will not change the operating principles of the apparatus.

[0047] According to the invention, the apparatus may be unilateral (i.e. associated with only one side of the mouth) or bilateral, upper or lower, anterior or posterior, covering the whole or only part the dental arches. Moreover, the elements of the apparatus may be integrated in a single piece, or comprising separate parts joined by a fixed or adjustable isthmus, covering partially any region of the dental arches, from a single tooth up to all teeth.

[0048] FIGS. 5-a, 5-b and 5-c show an embodiment of the invention in which the sensors, instead of being located on the sides of the dental arch as exemplified in FIG. 4-a, are embedded in a unit 21 placed in the front portion of the same, that is, associated with the incisor teeth. This embodiment uses only one active device placed next to the inner region of the teeth 13, in which the sensor 15, the microprocessor (not shown) and the electronic elements 17, are located. The operating principle is the same as previously described, the sensor 15 being pressed by the upper edges of the lower incisors.

[0049] Another embodiment of the invention is shown in FIGS. 6-a, 6-b and 6-c. According to these figures, this embodiment employs only the lower mouth guard 22, which is installed in the lower dental arch of the patient. The sensor element 15, which covers the upper edges of the lower dental arch incisors, is electrically connected to the electronic components 17, 18, which operate in the manner described above in connection with the embodiments of FIGS. 4 and 5.

[0050] Although FIG. 6-a shows two active devices, located on the right and left sides of the dental arch, the apparatus may employ only one of these active devices, positioned either on the left or on the right side. Such an embodiment is shown in FIG. 8, employing only one active device situated, in this example, on the right-hand side 23a of the mouth guard 23. As shown in this figure, the mouth guard comprises a left-side branch extension 23b in order to provide a balanced occlusion.

[0051] The invention provides two ways of installing the apparatus into the patient's mouth. In a first embodiment, shown in FIG. 7, the engagement of one or both of the mouth guards is done by the dentist, using heavy or light silicone resins of addition or condensation such as acryline resin, resilient resins, or other materials available for the relining of prostheses.

[0052] In the case of installation by the patient, thermo-activated plastics will be used and, after preheating, can be molded in the mouth as is done with sports mouth guards such as, for example, those used in boxing. In such an embodiment of the invention, wherein the patient himself makes the installation, the active device is embedded in a thermo-activated synthetic resin, which is a material that softens when immersed in hot water. Once softened, the user can manipulate it in order to adapt it to his dental arch, and the apparatus will remain fixed after cooling.

[0053] While the present invention has been described in connection with preferred embodiments, it is to be understood that the invention is not to be limited to those particular embodiments. Rather, it is intended to cover all possible alternatives, modifications and equivalents within the spirit and scope of the invention.