The present invention relates generally to an interface system. More particularly, the present invention relates to an interface system, and a method for monitoring and controlling respiratory function of a user during a sleep session.
During medical treatments, it may be sometimes desirable to deliver a flow of breathing gas non-invasively to an airway of a patient, i.e., without intubating the patient or surgically inserting a tracheal tube in their trachea. For example, it is known to ventilate a patient using a technique known as non-invasive ventilation. It is also known to deliver continuous positive airway pressure (CPAP) or variable airway pressure, which varies with the patient's respiratory cycle, to treat a medical disorder, such as sleep apnea syndrome, in particular, obstructive sleep apnea (OSA).
Non-invasive ventilation and pressure support therapies may involve the placement of a patient interface device in combination with a tubing assembly on a head of the patient. The patient interface device may comprise, without limitation, a nasal mask that covers the patient's nose, a nasal cushion having nasal prongs that are received within the patient's nares/nostrils, a nasal/oral mask that covers the nose and mouth, or a full-face mask that covers the patient's face. The patient interface device interfaces the ventilator or pressure support device with the airway of the patient, so that a flow of breathing gas can be delivered from a pressure/flow generating device to the airway of the patient.
During a sleep session, a person usually progresses through some stages of non-rapid eye movement (NREM) sleep and then enters REM sleep. Some patients suffering from OSA tend to open their mouths during the sleep session as they try to breathe in more amount of oxygen. Particularly, due to relaxing of muscles in deep sleep stages, a frequency of mouth opening is increased in deep sleep stages comprising one or more NREM sleep stages and REM stage. A positive air pressure in the mouth during the relaxing of the muscles may also provide an additional force for opening the mouth in the deep sleep stages. The opening of mouth may compromise an effectiveness of the CPAP therapy used by the patients suffering from OSA. For the sleep apnea patients, mouth opening during deep sleep may cause air provided by the CPAP therapy to leak out of the mouth, thereby leading to sore mouth and drying of sinuses, mouth, and throat. In some cases, a patient may wake up due to air leakage when the mouth is open in the sleep session.
The leakage due to relaxing muscles can be prevented by using a full-face mask that covers the nose and mouth of the patient. However, many people find a full-face mask unattractive because of the mask leaks, inconvenience of sleeping on side, and claustrophobic experience for a user. The main applications of the current invention are in mask types that do not cover the mouth of the user, for example, so called nasal masks or nasal pillow masks.
In nasal masks, the conventional ways to prevent the mouth from opening during deep sleep include use of a fixed chin strap to keep the mouth closed during the sleep session. Another conventional way is to use a medical tape to close the lips of the sleep apnea patient in order to prevent the mouth from opening. The conventional ways may be uncomfortable for the sleep apnea patient. Moreover, the conventional ways to prevent the mouth from opening may create a feeling of claustrophobia and a fear of suffocation for the sleep apnea patient if the airflow through the nose is interrupted or obstructed for some reason (e.g., functional faults in tubing assembly, nasal masks, compressor of the CPAP, etc.). Therefore, the conventional ways to prevent the mouth from opening in the sleep apnea patients during deep sleep may be uncomfortable and counterproductive.
Accordingly, a first aspect of the present invention relates to an interface system for a user. The interface system comprises an interface unit configured to engage and selectively apply a force on a lower jaw of the user. The interface system further comprises an actuating unit operatively coupled to the interface unit. The actuating unit is configured to actuate the interface unit in order to selectively apply and adjust the force on the lower jaw of the user. The interface system further comprises one or more sensors configured to generate output signals conveying information related to sleep stages of the user during a sleep session. The interface system further comprises a processor communicably coupled to the one or more sensors and the actuating unit. The processor is configured to receive the output signals from the one or more sensors and determine a current sleep stage of the user during the sleep session. The processor is further configured to control the actuating unit based on the current sleep stage of the user to adjust the force applied by the interface unit on the lower jaw of the user, thereby adjusting a degree of mouth opening of the user.
Accordingly, a second aspect of the present invention relates to a method for monitoring and controlling respiratory function of a user during a sleep session. The method comprises engaging a lower jaw of the user with an interface unit. The interface unit is configured to selectively apply a force on a lower jaw of the user. The method further comprises providing an actuating unit operatively coupled to the interface unit. The actuating unit is configured to actuate the interface unit in order to selectively apply and adjust the force on the lower jaw of the user. The method further comprises receiving, via the processor, output signals from one or more sensors conveying information related to sleep stages of the user during the sleep session. The method further comprises determining, via the processor, a current sleep stage of the user based on the output signals received from the one or more sensors. The method further comprises controlling, via the processor, the actuating unit based on the current sleep stage of the user to adjust the force applied by the interface unit on the lower jaw of the user, thereby adjusting a degree of mouth opening of the user.
A third aspect of the present invention relates to an interface system for monitoring and controlling respiratory function of a user. The interface system comprises interface means for engaging and selectively applying a force on a lower jaw of the user. The interface system further comprises actuating means for actuating the interface unit in order to selectively apply and adjust the force on the lower jaw of the user. The interface system further comprises sensor means for generating output signals conveying information related to sleep stages of the user during a sleep session. The interface system further comprises processing means for determining a current sleep stage of the user based on the output signals received from the sensor means. The processing means further controls the actuating means based on the current sleep stage of the user to adjust the force applied by the interface means on the lower jaw of the user, thereby adjusting a degree of mouth opening of the user.
A general object of the present invention is to provide an interface system for a user. The interface system is used during a sleep session to adjust a degree of mouth opening of the user during the sleep session based on a current sleep stage of the user. The degree of mouth opening of the user is controlled by selectively applying and adjusting a force applied by the interface system on a lower jaw of the user.
These and other objects, features, and characteristics of the present invention, as well as the methods of operation and functions of the related elements of structure and the combination of parts and economies of manufacture, will become more apparent upon consideration of the following description and the appended claims with reference to the accompanying drawings, all of which form a part of this specification, wherein like reference numerals designate corresponding parts in the various figures. It is to be expressly understood, however, that the drawings are for the purpose of illustration and description only and are not intended as a definition of the limits of the scope of the appended claims.
Exemplary embodiments disclosed herein may be more completely understood in consideration of the following detailed description in connection with the following figures. The figures are not necessarily drawn to scale. Like numbers used in the figures refer to like components. However, it will be understood that the use of a number to refer to a component in a given figure is not intended to limit the component in another figure labeled with the same number.
In the following description, reference is made to the accompanying figures that form a part thereof and in which various embodiments are shown by way of illustration. It is to be understood that other embodiments are contemplated and may be made without departing from the scope or spirit of the appended claims. The following detailed description, therefore, is not to be taken in a limiting sense.
As used herein, the singular form of “a”, “an”, and “the” include plural references unless the context clearly dictates otherwise. As used herein, the statement that two or more parts or components are “coupled” shall mean that the parts are joined or operate together either directly or indirectly, i.e., through one or more intermediate parts or components, so long as a link occurs. As used herein, the phrase “sealingly engage” shall mean elements which contact each other in a manner such that a generally air-tight seal is formed therebetween.
Directional phrases used herein, such as, for example and without limitation, top, bottom, left, right, upper, lower, front, back, and derivatives thereof, relate to the orientation of the elements shown in the drawings and are not limiting upon the claims unless expressly recited therein.
Referring to
Pressure generating device 16 may comprise, without limitation, ventilators, constant pressure support devices (such as a continuous positive airway pressure device, or CPAP device), variable pressure devices (e.g., BiPAP®, Bi-Flex®, or C-Flex™ devices manufactured and distributed by Philips Respironics of Murrysville, Pa.), and auto-titration pressure support devices. Conduit 18, tubing assembly 14, and respiratory interface device 12 are often collectively referred to as a user circuit.
Respiratory interface device 12 comprises a respiratory sealing element 13. In an exemplary embodiment, respiratory sealing element 13 may comprise a nasal cushion made of a soft, flexible material, such as, without limitation, silicone, an appropriately soft thermoplastic elastomer, a closed-cell foam, or any other suitable material or combination of such materials. It is to be appreciated, however, that any type of respiratory sealing element 13, such as a nasal/oral mask, a nasal pillow, or a full-face mask, which may facilitate a delivery of the flow of breathing gas to the airway of user 10, may be used in respiratory interface device 12. It should be noted that tubing assembly 14, in conjunction with additional attachments, may allow coupling of different types of respiratory interface devices, without any limitations.
Interface system 100 further comprises one or more sensors 106 configured to generate output signals 108 conveying information related to sleep stages of user 10 during a sleep session. In various exemplary embodiments, one or more sensors 106 may be interchangeably referred to as “sensor means 106”. Therefore, interface system 100 comprises sensor means 106 for generating output signals 108 conveying information related to sleep stages of user 10 during the sleep session. Output signals 108 conveying information related to sleep stages of user 10 may include information related to brain activity in user 10, cardiac activity in user 10, and/or other physiological activity in user 10. As such, one or more sensors 106 are configured to generate output signals 108 conveying information related to brain activity, cardiac activity, and/or other activity in user 10. In various exemplary embodiments, one or more sensors 106 are configured to generate output signals 108 conveying information related to stimulation provided to user 10 during sleep sessions. In other embodiments, information conveyed by output signals 108 from one or more sensors 106 may be used to control a sensory stimulator to provide sensory stimulation to user 10.
In the illustrated embodiment of
In various exemplary embodiments, one or more sensors 106 comprise at least one of an electroencephalogram (EEG) sensor, an electrocardiogram (ECG) sensor, a photoplethysmography (PPG) sensor, an air flow sensor, a microphone, a humidity sensor, a carbon dioxide sensor, an accelerometer, a bioimpedance sensor, and an image sensor.
In various exemplary embodiments, one or more sensors 106 may generate output signals 108 that directly convey information related to brain activity of user 10. For example, one or more sensors 106 may include EEG electrodes configured to detect electrical activity along the scalp of user 10 resulting from current flows within the brain of user 10. In various exemplary embodiments, one or more sensors 106 may generate output signals 108 that indirectly convey information related to brain activity of user 10. For example, one or more sensors 106 may comprise a heart rate sensor that generates an output based on a heart rate of user 10 (e.g., a sensor 106 may be a heart rate sensor than can be located on the chest of user 10, and/or be configured as a bracelet on a wrist of user 10, and/or be located on another limb of user 10). In various exemplary embodiments, one or more sensors 106 may generate output signals 108 based on a movement of user 10, a respiration of user 10, and/or other characteristics of user 10.
In various exemplary embodiments, one or more sensors 106 comprising the accelerometer may be carried or disposed on a wearable device, such as a bracelet around the wrist and/or ankle of user 10, such that sleep may be analyzed using actigraphy signals. In various exemplary embodiments, one or more sensors 106 comprising the bioimpedance sensor enable measuring important physiological parameters required to determine the current sleep stage of user 10. For example, the bioimpedance sensor may be used to perform brain and pulmonary function monitoring, impedance cardiography, pneumography, and so on.
In various exemplary embodiments, one or more sensors 106 may comprise an electrooculogram (EOG) electrode, an actigraphy sensor, an ECG electrode, a respiration sensor, a pressure sensor, a vital signs camera, a functional near infra-red sensor (fNIR), a temperature sensor, and/or other sensors configured to generate output signals 108 related to (e.g., the quantity, frequency, intensity, and/or other characteristics) the stimulation provided to user 10, the brain activity of user 10, the cardiac activity of user 10, and/or any other physiological parameter of user 10.
In various exemplary embodiments, one or more sensors 106 may be grouped into one or more singular devices. For example, one or more sensors 106 may be included in a headset and/or other garments worn by user 10. Such a headset may include, for example, sensing electrodes, a reference electrode, and one or more devices associated with an EEG. The reference electrode may be located behind the ear of user 10 or in other locations. In this example, the sensing electrodes may be configured to generate output signals 108 conveying information related to brain activity of user 10, and sleep stages of user 10 during the sleep session.
In various exemplary embodiments, at least one of one or more sensors 106 is configured to detect a degree of mouth opening of user 10. For example, one or more sensors 106 comprising the accelerometer may detect changes in mouth opening of user 10 during the sleep session.
Interface system 100 further comprises a processor 20 communicably coupled to one or more sensors 106. Processor 20 may be a programmable analog and/or digital device that can store, retrieve, and process data. In an application, processor 20 may be a controller, a control circuit, a computer, a workstation, a microprocessor, a microcomputer, a central processing unit, a server, or any suitable device or apparatus. Processor 20 may comprise one or more of a digital processor, an analog processor, a digital circuit designed to process information, an analog circuit designed to process information, a state machine, and/or other mechanisms for electronically processing information. In other embodiments, processor 20 may comprise a plurality of processing units. These processing units may be physically located within interface system 100, or the processing units may be located remotely from interface system 100. In various exemplary embodiments, processor 20 may be interchangeably referred to as “processing means 20”.
Processor 20 is configured to receive output signals 108 from one or more sensors 106 and determine a current sleep stage of user 10 during the sleep session. In other words, interface system 100 comprises processing means 20 for determining the current sleep stage of user 10 based on output signals 108 received from sensor means 106. Processor 20 may detect and/or predict the current sleep stage of user 10 based on various methods. For example, one of the methods to detect the current sleep stage of user 10 is provided in U.S. patent application Ser. No. 16/724,536, filed Dec. 23, 2019, entitled “System and method for enhancing rem sleep with sensory stimulation”, the contents of which are incorporated herein by reference.
Initially, according to the method, a machine learning model is trained by using historical sleep stage information associated with one or more users. In various exemplary embodiments, the machine learning model is trained by providing the historical sleep stage information as an input to the machine learning model. In various exemplary embodiments, the machine learning model may be and/or include mathematical equations, algorithms, plots, charts, networks (e.g., neural networks), and/or other tools, and machine learning model components. For example, the machine learning model may be and/or include one or more neural networks having an input layer, an output layer, and one or more intermediate or hidden layers, and/or any other supervised machine learning algorithms. In various exemplary embodiments, the one or more neural networks and/or any other supervised machine learning algorithms may be and/or include deep neural networks (e.g., neural networks that have one or more intermediate or hidden layers between the input and output layers). Therefore, processor 20 may detect the current sleep stage of user 10 based on output signals 108 and the machine learning model comprising neural networks.
The current sleep stage detected by processor 20 may be associated with REM sleep, non-rapid eye movement (NREM) sleep, and/or other sleep. For example, the current sleep stage detected by processor 20 may be a first NREM sleep stage N1 (shown in
With reference to
One may consider that force F is applied to lower jaw 22 and another, equivalent counterforce is applied to the skull to keep it immobilized. Similarly, one may consider that the same angular momentum on the hinge may be created by applying a force to the skull and a support to lower jaw 22. The effect on the temporomandibular joint in both cases is an angular momentum, which acts towards closing of the mouth. In a case of a strap, we have a full duality, and these two interpretations are equivalent. In the following description and the claims we state, for brevity, that the “force is applied to the lower jaw” but it should be clear based on elementary physics that equivalent dual interpretations of the directions of the acting forces is possible.
In various exemplary embodiments, force F may be applied to electrically stimulate the mandibular branch of the trigeminal nerve. The electrical stimulation of the mandibular branch may further cause the masseter muscle to contract which acts towards closing of the mouth.
In various exemplary embodiments, interface unit 102 may be interchangeably referred to as “interface means 102”. Therefore, interface system 100 comprises interface means 102 for engaging and selectively applying force F on lower jaw 22 of user 10. In the illustrated embodiment of
In
With reference to
In various exemplary embodiments, interface unit 102 further comprises a headband 210 (shown in
In various exemplary embodiments, one or more sensors 106 comprise a set of first sensors 106A disposed on first lateral portion 206 of strap 202 and a set of second sensors 106B disposed on second lateral portion 208 of strap 202. In other embodiments, one or more sensors 106 may further comprise additional sets of sensors disposed on various locations on strap 202. In other embodiments, one or more sensors 106 may further comprise additional sets of sensors 106 disposed in other locations outside strap 202 or interface unit 102.
Interface system 100 further comprises an actuating unit 104 operatively coupled to interface unit 102. Specifically, actuating unit 104 is configured to actuate interface unit 102 in order to selectively apply and adjust force F on lower jaw 22 of user 10. In various exemplary embodiments, actuating unit 104 may be interchangeably referred to as “actuating means 104”. Therefore, interface system 100 comprises actuating means 104 for actuating interface unit 102 in order to selectively apply and adjust force F on lower jaw 22 of user 10. Actuating unit 104 is schematically shown in
Processor 20 is communicably coupled to actuating unit 104. Processor 20 (or processing means 20) is further configured to control actuating unit 104 (or actuating means 104) based on the current sleep stage of user 10 to adjust force F applied by interface unit 102 on lower jaw 22 of user 10, thereby adjusting a degree of mouth opening of user 10. Therefore, processor 20 is configured to control actuating unit 104 based on the degree of mouth opening of user 10. In the illustrated embodiment of
Actuating unit 104 further comprises a head spring 310 configured to be disposed on head 30 of user 10 and coupled to each of first lateral spring 306 and second lateral spring 308. Head spring 310 is coupled to headband 210. In various exemplary embodiments, each of head spring 310, first lateral spring 306, and second lateral spring 308 is directly or indirectly coupled to each other via a string 309. In various exemplary embodiments, each of head spring 310, first lateral spring 306, and second lateral spring 308 may be a coil spring.
Actuating unit 104 further comprises a first motor mechanism 312 operatively coupled to first lateral spring 306 and configured to extend or compress first lateral spring 306. Actuating unit 104 further comprises a second motor mechanism 314 operatively coupled to second lateral spring 308 and configured to extend or compress second lateral spring 308. Processor 20 is communicably coupled to each of first motor mechanism 312 and second motor mechanism 314.
Extension or compression of each of first lateral spring 306 and second lateral spring 308 causes a corresponding compression or extension of head spring 310. In the illustrated embodiment of
Further, first motor mechanism 312 and second motor mechanism 314 are configured to extend or compress first lateral spring 306 and second lateral spring 308, respectively, by adjusting a tension in string 309. For example, first motor mechanism 312 and second motor mechanism 314 are configured to compress first lateral spring 306 and second lateral spring 308, respectively, by pulling string 309. Compression of first lateral spring 306 and second lateral spring 308 results in extension of head spring 310.
In various exemplary embodiments, each of first motor mechanism 312 and second motor mechanism 314 may comprise at least a rotor, a stator surrounding the rotor, an output shaft, and a winding. Components of first motor mechanism 312 and second motor mechanism 314 are not shown in
In the illustrated embodiment of
Referring to
In various exemplary embodiments, processor 20 is further configured to increase force F applied by interface unit 102 in a stepwise manner to a first force level F1 from idle force level F0 corresponding to awake state A1 upon detection of first NREM sleep stage N1. In other words, once user 10 transitions from awake state A1 to first NREM sleep stage N1 during the sleep session, processor 20 receives output signals 108 conveying information related to first NREM sleep stage N1, and force F applied by interface unit 102 is increased from idle force level FO to first force level F1. Specifically, upon detection of first NREM sleep stage N1, processor 20 controls actuating unit 104, such that force F applied by interface unit 102 equals first force level F1. With reference to
Processor 20 is further configured to increase force F applied by interface unit 102 in a stepwise manner to a second force level F2 from first force level F1 upon detection of second NREM sleep stage N2. In other words, once user 10 transitions from first NREM sleep stage N1 to second NREM sleep stage N2 during the sleep session, processor 20 receives output signals 108 conveying information related to second NREM sleep stage N2, and force F applied by interface unit 102 is increased from first force level F1 to second force level F2. Specifically, upon detection of second NREM sleep stage N2, processor 20 controls actuating unit 104, such that force F applied by interface unit 102 equals second force level F2. With reference to
Processor 20 is further configured to increase force F applied by interface unit 102 in a stepwise manner to a third force level F3 from second force level F2 upon detection of REM sleep stage R1. In other words, once user 10 transitions from second NREM sleep stage N2 to REM sleep stage R1 during the sleep session, processor 20 receives output signals 108 conveying information related to REM sleep stage R1, and force F applied by interface unit 102 is increased from second force level F2 to third force level F3. Specifically, upon detection of REM sleep stage R1, processor 20 controls actuating unit 104, such that force F applied by interface unit 102 equals third force level F3. With reference to
From graph 400, it can be concluded that force F applied by interface unit 102 on lower jaw 22 is greater in REM sleep stage R1 and second NREM sleep stage N2 as compared to force F applied by interface unit 102 in first NREM sleep stage N1 and awake state of user 10. With reference to
In various embodiments, processor 20 is further configured to progressively increase force F applied by interface unit 102 on lower jaw 22 based on a progression of the sleep stages of user 10 from awake state A1 to REM sleep stage R1. Upon progression of the sleep stages of user 10 from awake state Al to REM sleep stage R1, processor 20 controls actuating unit 104 to actuate interface unit 102, such that force F applied by interface unit 102 on lower jaw 22 is progressively increased from idle force level F0 to third force level F3. With reference to
In various exemplary embodiments, during the sleep session, processor 20 controls actuating unit 104, such that mouth opening of user 10 in each of second NREM sleep stage N2 and REM sleep stage R1 is substantially the same as the mouth opening of user 10 in first NREM sleep stage N1, or awake state A1 of user 10.
Referring to
In various exemplary embodiments, processor 20 is further configured to close the mouth of user 10 upon detection of REM sleep stage R1. Once processor 20 receives output signals 108 conveying information related to REM sleep stage R1, processor 20 controls actuating unit 104 (i.e., first and second motor mechanisms 312, 314) in order to adjust (i.e., increase) force F applied by strap 202 on lower jaw 22 of user 10. Specifically, upon receiving output signals 108 conveying information related to REM sleep stage R1, processor 20 controls actuating unit 104 in order to increase the tightness of strap 202 and prevent the mouth of user 10 from opening.
In various exemplary embodiments, processor 20 is further configured to remove force F applied by interface unit 102 upon detection of awake state A1 of user 10 or an emergency medical event. With reference to
In various exemplary embodiments, processor 20 is further configured to decrease force F applied by interface unit 102 upon detection of a transition from REM sleep stage R1 to another sleep stage. In an example, upon detection of a transition from REM sleep stage R1 to at least one of awake state A1, first NREM sleep stage N1, and second NREM sleep stage N2, processor 20 controls actuating unit 104 to decrease force F applied by interface unit 102 on lower jaw 22 of user 10. With reference to
In various exemplary embodiments, processor 20 is further configured to decrease force F applied by interface unit 102 upon detection of a bruxism event during the sleep session. In other words, upon detection of the bruxism event during the sleep session, processor 20 controls actuating unit 104 to decrease force F applied by interface unit 102 on lower jaw 22 of user 10. With reference to
In various exemplary embodiments, user 10 may be a sleep apnea patient. With reference to
Moreover, by adjusting the degree of mouth opening of user 10 during the sleep session, the CPAP therapy may also benefit user 10 effectively. Hence, if the mouth opening of user 10 is controlled by interface system 100, there may be minimal leakage of air (provided by the CPAP therapy) out of the mouth of user 10, which may otherwise cause dryness in the sinuses, throat, and mouth. Further, due to minimal air leakage out of the mouth of user 10, user 10 may not wake up during the sleep session, which could have otherwise happened in case of air leakage in the absence of interface system 100. In this way, interface system 100 comprising interface unit 102 monitors and controls respiratory function of user 10 during the sleep session.
As the degree of mouth opening of user 10 is adjusted during the deep sleep (i.e., second NREM sleep stage N2 and REM sleep stage R1), user 10 may not feel uncomfortable in contrast to the conventional ways of preventing the mouth opening by using a medical tape or a fixed chain strap. Actuating unit 104 is configured to tighten strap 202 for preventing the mouth of user 10 from opening only when user 10 tends to open the mouth during the deep sleep. Therefore, user 10 may not feel uncomfortable while wearing interface unit 102 during the sleep session and receiving the air from the CPAP therapy. Moreover, force F (shown in
While interface unit 102 is preventing the mouth of user 10 from opening during the deep sleep, one or more sensors 106 continuously measure critical parameters of user 10. For example, the PPG sensors continuously measure blood oxygen saturation of user 10. In case of any emergency situation or emergency medical condition, such as abnormal blood oxygen levels, congestion, nasal obstruction, lack of air, and functional faults in the CPAP therapy, processor 20 receives corresponding output signals 108 from one or more sensors 106, and thereby controls actuating unit 104 to adjust or reduce force F applied by interface unit 102 on lower jaw 22 of user 10. In case of emergency situations, interface system 100 does not apply force F to close the mouth opening of user 10 in the deep sleep. Hence, user 10 may not experience a feeling of claustrophobia and a fear of suffocation if there is any fault in the CPAP therapy that would affect the supply of air to user 10.
In various exemplary embodiments, robotic arm 602 may be configured to apply force F (shown in
Typically, a mouthguard may help in relieving obstructive sleep apnea in a person. In various exemplary embodiments, in interface system 700, actuating unit 104 may comprise motor mechanism 604 (shown in
At step 802, method 800 comprises engaging lower jaw 22 (shown in
There is thus provided an interface system and a method for monitoring and controlling respiratory function of a user, which overcomes the existing problems. While the invention has been illustrated and described in detail in the drawings and foregoing description, such illustration and description are to be considered illustrative or exemplary and not restrictive; the invention is not limited to the disclosed embodiments. Other variations to the disclosed embodiments can be understood and effected by those skilled in the art in practicing the claimed invention, from a study of the drawings, the disclosure, and the appended claims.
In the claims, the word “comprising” does not exclude other elements or steps, and the indefinite article “a” or “an” does not exclude a plurality. The mere fact that certain measures are recited in mutually different dependent claims does not indicate that a combination of these measures cannot be used to advantage.
In the present invention, the expression “at least one of A, B and C” means “A, B, and/or C”, and that it suffices if, for example, only B is present. A single element or other unit may fulfill the functions of several items recited in the claims. The mere fact that certain measures are recited in mutually different dependent claims does not indicate that a combination of these measures cannot be used to advantage. Any reference signs placed between parentheses in the claims should not be construed as limiting the scope of the appended claims.
This patent application claims the priority benefit under 35 U.S.C. § 119(e) of U.S. Provisional Application No. 62/286,680, filed on Dec. 7, 2021, the contents of which are herein incorporated by reference.
Number | Date | Country | |
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63286680 | Dec 2021 | US |