Method and apparatus for treating sleep apnea
An oral appliance provides electrical stimulation to a patient's tongue in a manner that prevents collapse of the tongue and/or soft palate during sleep. More specifically, the appliance may induce a reversible current or currents in a lateral direction across the tongue in a manner that shortens the patient's Palatoglossus muscle, which in turn pulls the patient's soft palate downward towards a base of the tongue, and/or decreases a volume of the tongue.
1. A device configured to provide electrical stimulation to an oral cavity of a patient, the device comprising:
an appliance including a body having first and second lateral arms each terminating in a posterior-most free end;
a first electrode including a first portion directly attached to a lingual side of the posterior-most free end of the first lateral arm and including a second portion extending posteriorly beyond the posterior-most free end of the first lateral arm;
a second electrode including a first portion directly attached to a lingual side of the posterior-most free end of the second lateral arm and including a second portion extending posteriorly beyond the posterior-most free end of the second lateral arm, wherein the first and second electrodes are configured to be angularly oriented with respect to a floor of the patient's mouth such that the first and second electrodes are adapted to face opposite lateral sides of the patient's tongue; and
a control circuit coupled to the appliance and to the electrodes, the control circuit configured to induce a current in a lateral direction across the tongue via the first and second electrodes to generate the electrical stimulation.
2. The device of claim 1 , wherein at least one of the electrodes is further configured to sense a respiration function of the patient.
3. The device of claim 2 , wherein the control circuit is further configured to:
provide one or more first signals to the at least one of the electrodes during a first mode, the one or more first signals configured to induce the current; and
receive a second signal from the at least one of the electrodes during a second mode, the second signal indicative of the patient's respiration function.
4. The device of claim 3 , wherein the control circuit is further configured to dynamically adjust the one or more first signals in response to the second signal.
5. The device of claim 1 , wherein the induced current comprises one or more reversible currents configured to flow in one or more substantially lateral directions across the tongue.
6. The device of claim 5 , wherein at least one of the reversible currents comprises a zero-sum waveform.
7. The device of claim 5 , wherein a pulse length of at least one of the reversible currents is configured according to a resistive-capacitive (RC) time constant model associated with the tongue.
8. The device of claim 1 , further comprising:
a power supply, mounted on the appliance, to provide power to the control circuit.
9. The device of claim 8 , wherein the appliance, the electrodes, the control circuit, and the power supply comprise a unitary device adapted to fit entirely within the patient's oral cavity.
10. The device of claim 1 , wherein the electrodes are configured to induce the current by providing a voltage differential across the tongue.
11. The device of claim 1 , wherein the first and second electrodes are adapted to be in contact with opposite sides of the patient's tongue proximate to lateral points at which a Palatoglossus muscle inserts into the tongue when the appliance is inserted within the oral cavity.
12. The device of claim 1 , wherein the electrodes are responsive to one or more signals generated by the control circuit.
13. The device of claim 1 , wherein the induced current is configured to shorten the patient's Palatoglossus muscle without targeting the patient's Hypoglossal nerve.
14. The device of claim 1 , wherein the induced current is configured to pull the patient's Palatoglossal arch in a downward direction towards a base of the tongue.
15. The device of claim 1 , wherein the induced current is configured to decrease a volume of the tongue without moving the tongue in an anterior direction.
16. The device of claim 1 , wherein one or more of the electrodes comprises an electromyogram (EMG) sensor configured to detect electrical activity of muscles within or connected to the patient's tongue.
17. The device of claim 1 , wherein the electrical stimulation is configured to avoid targeting a genioglossus muscle of the patient.
18. The device of claim 1 , wherein the electrical stimulation is configured to avoid targeting a hypoglossal nerve of the patient.
19. The device of claim 1 , wherein the device is removable.
20. The device of claim 1 , wherein at least one of the electrodes is further configured to detect snoring in the patient.
21. The device of claim 1 , wherein at least a portion of each of the first and second electrodes is adapted to be positioned posterior to a last molar location of the patient when the appliance is inserted within the oral cavity.
22. An appliance adapted to fit at least partially within and configured to provide electrical stimulation to a patient's oral cavity, the appliance comprising:
a body having first and second lateral arms each terminating in a posterior-most free end;
a first electrode including a first portion directly attached to a lingual side of the posterior-most free end of the first lateral arm and including a second portion extending posteriorly beyond the posterior-most free end of the first lateral arm;
a second electrode including a first portion directly attached to a lingual side of the posterior-most free end of the second lateral arm and including a second portion extending posteriorly beyond the posterior-most free end of the second lateral arm, wherein the first and second electrodes are configured to be angularly oriented with respect to a floor of the patient's mouth such that the first and second electrodes are adapted to contact opposite sublingual sides of the patient's tongue proximate to lateral points at which a Palatoglossus muscle inserts into the tongue; and
a control circuit coupled to the appliance and to the electrodes, the control circuit configured to induce a current in a lateral direction across the tongue via the first and second electrodes to generate the electrical stimulation.
23. The appliance of claim 22 , wherein at least one of the electrodes is further configured to sense a respiration function of the patient.
24. The appliance of claim 23 , wherein the control circuit is further configured to:
provide one or more first signals to the at least one of the electrodes during a first mode; and
receive a second signal from the at least one of the electrodes during a second mode, the second signal indicative of the patient's respiration function.
25. The appliance of claim 24 , wherein the control circuit is further configured to dynamically adjust the one or more first signals in response to the second signal.
26. The appliance of claim 22 , wherein the induced current comprises a reversible current.
27. The appliance of claim 26 , wherein the reversible current is configured to decrease a volume of the tongue.
28. The appliance of claim 26 , wherein the reversible current comprises a zero-sum waveform.
29. The appliance of claim 26 , wherein a pulse length of the reversible current is configured according to a resistive-capacitive (RC) time constant model associated with the tongue.
30. The appliance of claim 22 , wherein the first and second electrodes are adapted to substantially face opposite lateral sides of the tongue.
31. The appliance of claim 22 , wherein the electrical stimulation is configured to target the patient's Palatoglossus muscle.
32. The appliance of claim 22 , wherein the electrical stimulation is configured to avoid targeting a hypoglossal nerve of the patient.
33. The appliance of claim 22 , wherein the device is removable.
34. The appliance of claim 22 , wherein at least one of the electrodes is further configured to detect snoring in the patient.
35. The appliance of claim 22 , wherein at least a portion of each of the first and second electrodes is adapted to be positioned posterior to a last molar location of the patient when the appliance is inserted within the oral cavity.