SYSTEMS AND METHODS FOR CONCURRENT AIRWAY STABILIZATION AND PULMONARY STRETCH RECEPTOR ACTIVATION

Abstract

Concurrent treatment of obstructive sleep apnea and hypertension in a patient, via a pressure generating device, includes providing a flow of treatment gas to an airway of a patient in accordance with an initial set of flow parameters with respect to an obstructive sleep apnea mode. Responsive to determining that the patient has achieved stable breathing while receiving the flow of treatment gas, the flow parameters are increased above the initial set of flow parameters with respect to a hyper-ventilation mode. The flow of treatment gas is then provided to the airway of the patient in accordance with the increased flow parameters for a predetermined period of time. The increased flow parameters are configured to bring the patient's breath into accordance with target patient breath parameters configured to inflate the patient's lungs beyond a threshold for activating pulmonary stretch receptors of the airway of the patient.

Claims

1. A method for concurrent treatment of obstructive sleep apnea and hypertension in a patient, the method comprising: a) providing a flow of treatment gas, via a gas flow generator and a controller coupled to the gas flow generator, to a patient airway, via a patient circuit coupled to the gas flow generator, in accordance with an initial set of flow parameters associated with an obstructive sleep apnea mode of the treatment; b) determining an achievement of a stable breathing condition, via the controller, while providing the flow of treatment gas in accordance with the initial set of flow parameters; c) increasing the flow parameters above the initial set of flow parameters, via the controller, to a set of increased flow parameters associated with a hyper-ventilation mode of the treatment, in response to determining the achievement of the stable breathing condition; and d) providing the flow of treatment gas, via the gas flow generator and the controller, to the patient airway, via the patient circuit, in accordance with the set of increased flow parameters associated with the hyper-ventilation mode so to trigger stretch receptors in patient lungs and reduce hypertension.

2. The method of claim 1, wherein providing the flow of treatment gas in accordance with the increased flow parameters comprises providing the flow of treatment gas until a predetermined period of time has elapsed, the increased flow parameters further being configured to bring the patient's breath into accordance with target patient breath parameters configured to inflate the patient's lungs by an additional 50-400% of nominal tidal volume beyond a first threshold for activating pulmonary stretch receptors of the airway of the patient and triggering a reflex, governed by the patient's autonomic nervous system, to dilate peripheral blood vessels.

3. The method of claim 2, further comprising: e) further increasing the flow parameters above the increased flow parameters in response to the predetermined period of time having elapsed; and f) providing the flow of treatment gas, via the gas flow generator and the controller, to the airway of the patient, via the patient circuit, in accordance with the further increased flow parameters for another predetermined period of time, the further increased flow parameters being associated with a continuation in the hyper-ventilation mode of the pressure generating device and further configured to bring the patient's breath into accordance with the target patient breath parameters configured to further inflate the patient's lungs by an additional 50-400% of the nominal tidal volume beyond a second threshold, different from the first threshold, for re-activating pulmonary stretch receptors of the airway of the patient and further re-triggering the reflex, governed by the patient's autonomic nervous system, to further dilate peripheral blood vessels, up to a maximum hyperinflation threshold that should not be exceeded.

4. The method of claim 3, further comprising repeatedly performing steps d) and e) until the controller determines an occurrence of an exit indicator indicative of exiting the hyper-ventilation mode.

5. The method of claim 4, further comprising providing the flow of treatment gas, via the gas flow generator and the controller, to the airway of the patient, via the patient circuit, in accordance with the initial set of flow parameters in response to determining, via the controller, the occurrence of the exit indicator.

6. The method of claim 5, wherein determining the occurrence of the exit indicator comprises determining, via the controller, an expiration of an overall time limit for the hyper-ventilation mode.

7. The method of claim 1, wherein increasing the flow parameters comprises increasing the flow parameters above the initial set of flow parameters by a first predetermined increment.

8. The method of claim 7, further comprising determining, via the controller, an occurrence of a stop condition while providing the flow of treatment gas, and responsive to determining the occurrence of the stop condition: decreasing the flow parameters, via the controller, below the increased flow parameters or below a set of further increased flow parameters; and providing the flow of treatment gas, via the gas flow generator and the controller, to the airway of the patient, via the patient circuit, in accordance with the decreased flow parameters.

9. The method of claim 8, wherein decreasing the flow parameters comprises decreasing the flow parameters below the increased flow parameters or below the further increased flow parameters by a second predetermined increment.

10. The method of claim 9, wherein the second predetermined increment is less than the first predetermined increment.

11. The method of claim 8, further comprising, determining, via the controller, a ceasing of the stop condition, and responsive to determining the ceasing of the stop condition: increasing the flow parameters, via the controller, above the decreased flow parameters; and providing the flow of treatment gas, via the gas flow generator and the controller, to the airway of the patient, via the patient circuit, in accordance with the increased flow parameters above the decreased flow parameters.

12. The method of claim 8, further comprising, determining, via the controller, a non-ceasing of the stop condition, and responsive to determining the non-ceasing of the stop condition: further decreasing the flow parameters, via the controller, below the decreased flow parameters; and providing the flow of treatment gas, via the gas flow generator and the controller, to the airway of the patient, via the patient circuit, in accordance with the further decreased flow parameters.

13. An airway pressure support system configured for concurrent treatment of obstructive sleep apnea and hypertension in a patient, comprising a gas flow generator; and a controller, wherein the controller is programmed to carry out the method of claim 1.

14. A non-transitory machine readable medium encoded with instructions executable by a controller for causing the controller to carry out the method of claim 1 for concurrent treatment of obstructive sleep apnea and hypertension in a patient.

15. A method for concurrent treatment of obstructive sleep apnea and hypertension in a patient, the method comprising: a) providing a flow of treatment gas, via a gas flow generator a controller coupled to the gas flow generator, to an airway of the patient, via a patient circuit coupled to the gas flow generator, in accordance with an initial set of flow parameters associated with an obstructive sleep apnea mode of the treatment; b) determining an achievement of a stable breathing condition, via the controller, while providing the flow of treatment gas in accordance with the initial set of flow parameters; c) increasing the flow parameters above the initial set of flow parameters, via the controller, to a set of increased flow parameters associated with a hyper-ventilation mode of the treatment, in response to determining the achievement of the stable breathing condition; d) providing the flow of treatment gas, via the gas flow generator and the controller, to the airway of the patient, via the patient circuit, in accordance with the increased flow parameters associated with a hyper-ventilation mode so to trigger stretch receptors in patient lungs and reduce hypertension for a predetermined period of time; e) determining, via the controller, whether a stop increasing indicator has occurred within the predetermined period of time, wherein, responsive to determining an occurrence of the stop increasing indicator, further determining, via the controller, whether an exit hyper-ventilation mode indicator has occurred, wherein, (i) responsive to determining an occurrence of the exit hyper-ventilation mode indicator, then exiting the hyper-ventilation mode and providing the flow of treatment gas, via the gas flow generator and the controller, to the airway of the patient in accordance with the initial set of flow parameters, otherwise, (ii) responsive to not determining the occurrence of the exit hyper-ventilation mode indicator, then returning to the act of providing the flow of treatment gas, via the gas flow generator and the controller, to the airway of the patient in accordance with the increased flow parameters, and wherein, responsive to not determining the occurrence of the stop increasing indicator, then further increasing the flow parameters above the increased flow parameters, via the gas flow generator and the controller, to the airway of the patient, via the patient circuit, in accordance with the further increased flow parameters for another predetermined period of time in a continuation of the hyper-ventilation mode so to re-trigger the stretch receptors in the patient lungs and continue to reduce hypertension.

16. The method of claim 15, further comprising determining, via the controller, an occurrence of a stop condition while providing the flow of treatment gas, and responsive to determining the occurrence of the stop condition: decreasing the flow parameters, via the controller, below the increased flow parameters or below the further increased flow parameters; and providing the flow of treatment gas, via the gas flow generator and the controller, to the airway of the patient, via the patient circuit, in accordance with the decreased flow parameters.

17. The method of claim 16, wherein increasing the flow parameters comprises increasing the flow parameters above the initial set of flow parameters by a first predetermined increment, wherein decreasing the flow parameters comprises decreasing the flow parameters below the increased flow parameters by a second predetermined increment, and wherein the second predetermined increment is less than the first predetermined increment.

18. The method of claim 16, further comprising, determining, via the controller, a non-ceasing of the stop condition, and responsive to determining the non-ceasing of the occurrence of the stop condition: further decreasing the flow parameters, via the controller, below the decreased flow parameters; and providing the flow of treatment gas, via the gas flow generator and the controller, to the airway of the patient, via the patient circuit, in accordance with the further decreased flow parameters.

19. The method of claim 16, further comprising, determining, via the controller, a ceasing of the stop condition, and responsive to determining the ceasing of the stop condition: determining, via the controller, whether a stable breathing condition of the patient has occurred, while providing the flow of treatment gas in accordance with the decreased flow parameters, wherein, responsive to determining that the stable breathing condition of the patient has occurred, then determining, via the controller, whether the stop increasing indicator has occurred and proceeding with the act e), and wherein, responsive to determining that the stable breathing condition of the patient has not occurred, then continuing with the act of providing the flow of treatment gas, via the gas flow generator and the controller, to the airway of the patient, via the patient circuit, in accordance with the decreased flow parameters.

20. The method of claim 15, further comprising determining, via the controller, an occurrence of an exit indicator, the exit indicator configured to indicate an expiration of an overall time limit for the hyper-ventilation mode, wherein responsive to determining the occurrence of the exit indicator, then providing the flow of treatment gas, via the gas flow generator and the controller, to the airway of the patient, via the patient circuit, in accordance with the initial set of flow parameters, otherwise, repeatedly performing the acts of d) and e) until the controller determines the occurrence of the exit indicator.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

[0022] FIG. 1 is a schematic diagram showing an airway pressure support system according to an exemplary embodiment of the present invention;

[0023] FIG. 2 is a schematic diagram of the pressure generating device of the pressure support system of FIG. 1;

[0024] FIG. 3 is a flowchart showing a method for concurrently stabilizing the airway of a patient and treating hypertension according to an exemplary embodiment of the present invention; and

[0025] FIG. 4 is a flowchart showing a method for concurrently stabilizing the airway of a patient and treating hypertension according to another exemplary embodiment of the present invention.

DETAILED DESCRIPTION OF EXEMPLARY EMBODIMENTS

[0026] 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, “directly coupled” means that two elements are directly in contact with each other. As used herein, “fixedly coupled” or “fixed” means that two components are coupled so as to move as one while maintaining a constant orientation relative to each other.

[0027] As used herein, the word “unitary” means a component is created as a single piece or unit. That is, a component that includes pieces that are created separately and then coupled together as a unit is not a “unitary” component or body. As employed herein, the statement that two or more parts or components “engage” one another shall mean that the parts exert a force against one another either directly or through one or more intermediate parts or components. As employed herein, the term “number” shall mean one or an integer greater than one (i.e., a plurality).

[0028] As used herein, “minute ventilation” or “MV” for short, refers to the volume of air breathed by a patient in a minute.

[0029] As used herein, “breath rate” or “BR” for short, refers to quantity of breaths a patient takes in a minute.

[0030] As used herein, “tidal volume” or “TV” for short, refers to the volume of air displaced by a patient during one of an inhalation or an exhalation.

[0031] As used herein, “lung compliance” or “LC” for short, refers generally to the stiffness of the patient's lungs.

[0032] As used herein, a breath “tail” of a patient, refers to the time between an exhalation and a subsequent inhalation by the patient.

[0033] 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.

[0034] Pulmonary stretch receptors are afferent nerve endings located throughout the airway (trachea, bronchi, and bronchioles). These nerve endings are attached to smooth muscle, collagen, and elastin fibers in the tissue membranes. Pulmonary stretch receptors are activated when the tissue is stretched, but slowly deactivate if the stretch is maintained. During normal breathing, these receptors are activated to some degree during each inspiration since the tissue is stretched/un-stretched cyclically over the course of each breath cycle. Stretching these receptors beyond the threshold of a typical breath (e.g., by inflating the lung by an additional 50-300% of nominal tidal volume) triggers a reflex, governed by the autonomic nervous system, to dilate peripheral blood vessels, which results in reduced blood pressure, especially in hypertensive patients. Embodiments of the present invention utilize such receptors to simultaneously and effectively treat both obstructive sleep apnea (OSA) and hypertension.

[0035] FIG. 1 shows a schematic diagram of an airway pressure support system 2 according to one particular, non-limiting exemplary embodiment of the present invention. Airway pressure support system 2 includes a pressure generating device 4, a schematic diagram of which is shown in FIG. 2. Referring to FIGS. 1 and 2, pressure generating device 4 includes a gas flow generator 6, such as a blower used in a conventional CPAP or bi-level pressure support device. Gas flow generator 6 receives breathing gas, generally indicated by arrow C, from the ambient atmosphere and generates a flow of breathing gas therefrom for delivery to an airway of a patient 10 at relatively higher and lower pressures, i.e., generally equal to or above ambient atmospheric pressure. In the exemplary embodiment, gas flow generator 6 is capable of providing a flow of breathing gas ranging in pressure from 3-30 cmH2O. The pressurized flow of breathing gas from gas flow generator 6, generally indicated by arrow D, is delivered via a delivery conduit 12 to a patient interface device 14 of any known construction, which is typically worn by or otherwise attached to patient 10 to communicate the flow of breathing gas to the airway of patient 10. Delivery conduit 12 and patient interface device 14 are typically collectively referred to as a patient circuit.

[0036] Pressure support system 2 shown in FIG. 1 is what is known as a single-limb system, meaning that the patient circuit includes only delivery conduit 12 connecting patient 10 to pressure support system 2. As such, an exhaust vent (not numbered) is provided in patient interface device 14 for venting exhaled gases from the system. It should be noted that the exhaust vent can be provided at other locations in addition to or instead of in patient interface device 14, such as in delivery conduit 12. It should also be understood that the exhaust vent can have a wide variety of configurations depending on the desired manner in which gas is to be vented from pressure support system 2.

[0037] The present invention also contemplates that pressure support system 2 can be a two-limb system, having a delivery conduit and an exhaust conduit connected to patient 10. In a two-limb system (also referred to as a dual-limb system), the exhaust conduit carries exhaust gas from patient 10 and includes an exhaust valve at the end distal from patient 10. The exhaust valve in such an embodiment is typically actively controlled to maintain a desired level of pressure in the system, which is commonly known as positive end expiratory pressure (PEEP).

[0038] In the illustrated embodiment, pressure generating device 4 includes a pressure controller in the form of a valve 16 provided in an internal delivery conduit 18 provided in pressure generating device 4. Valve 16 controls the pressure of the flow of breathing gas from gas flow generator 6 that is delivered to patient 10. For present purposes, gas flow generator 6 and valve 16 are collectively referred to as a pressure generating system because they act in concert to control the pressure and/or flow of gas delivered to patient 10. However, it should be apparent that other techniques for controlling the pressure of the gas delivered to patient 10, such as varying the blower speed of gas flow generator 6, either alone or in combination with a pressure control valve, are contemplated by the present invention. Thus, valve 16 is optional depending on the technique used to control the pressure of the flow of breathing gas delivered to patient 10. If valve 16 is eliminated, the pressure generating system corresponds to gas flow generator 6 alone, and the pressure of gas in the patient circuit is controlled, for example, by controlling the motor speed of gas flow generator 6.

[0039] Pressure generating device 4 further includes a flow sensor 20 that measures the flow of the breathing gas within delivery conduit 18 and delivery conduit 12. In the particular embodiment shown in FIG. 2, flow sensor 20 is interposed in line with delivery conduits 18 and 12, most preferably downstream of valve 16. Flow sensor 20 generates a flow signal, QMEASURED, that is provided to a controller 22 and is used by controller 22 to determine the flow of gas at patient 10 (QPATIENT).

[0040] Techniques for calculating QPATIENT based on QMEASURED are well known, and take into consideration the pressure drop of the patient circuit, known leaks from the system, i.e., the intentional exhausting of gas from the circuit as described herein, and unknown (unintentional) leaks from the system, such as leaks at the mask/patient interface. The present invention contemplates using any known or hereafter developed technique for calculating total leak flow QLEAK, and using this determination in calculating QPATIENT based on QMEASURED (and for other purposes as described elsewhere herein). Examples of such techniques are taught by U.S. Pat. Nos. 5,148,802; 5,313,937; 5,433,193; 5,632,269; 5,803,065; 6,029,664; 6,539,940; 6,626,175; and 7,011,091, the contents of each of which are incorporated by reference into the present invention.

[0041] Of course, other techniques for measuring the respiratory flow of patient 10 are contemplated by the present invention, such as, without limitation, measuring the flow directly at patient 10 or at other locations along delivery conduit 12, measuring patient flow based on the operation of gas flow generator 6, and measuring patient flow using a flow sensor upstream of valve 16. Patient flow can be integrated during inspiration to produce a tidal volume.

[0042] Controller 22 includes a processing portion which may be, for example, a microprocessor, a microcontroller or some other suitable processing device, and a memory portion that may be internal to the processing portion or operatively coupled to the processing portion and that provides a storage medium for data and software executable by the processing portion for controlling the operation of pressure support system 2.

[0043] An input/output device 23 is provided for setting various parameters used by airway pressure support system 2, as well as for displaying and outputting information and data to a user, such as a clinician or caregiver.

[0044] Furthermore, in the illustrated embodiment, pressure generating device 4 also includes a humidifier 24. Alternatively, humidifier 24 may be separate from and located external to pressure generating device 4. Humidifier 24 is controlled by controller 22. Humidifier 24 further improves comfort by providing moisture in the supplied gas. In the exemplary embodiment, humidifier 24 is a passover type humidifier. U.S. Patent Application Publication No. 2007/0169776, incorporated herein by reference in its entirety, discloses an exemplary humidifier device suitable for use in the present invention. Humidifier devices having alternative designs, such as a non-passover type humidifier that employs nebulization, atomization, vaporization or a combination thereof, may also be used.

[0045] Pressure generating device 4 also includes a pressure sensor 26 that measures the pressure of the breathing gas within delivery conduit 18 and delivery conduit 12. In the particular embodiment shown in FIG. 2, pressure sensor 26 is interposed in line with delivery conduits 18 and 12, downstream of valve 16. Pressure sensor 26 generates a pressure signal (not labeled), that is provided to controller 22 and is used by controller 22 in carrying out the methods described further herein.

[0046] In the exemplary embodiment, patient interface device 14 includes a patient sealing assembly 28, which in the illustrated embodiment is a full face mask. However, other types of patient interface devices, such as, without limitation, a nasal mask, a nasal/oral mask, or a nasal cushion, which facilitate the delivery of the flow of breathing gas to the airway of a patient may be substituted for patient sealing assembly 28 while remaining within the scope of the present invention. A fluid coupling conduit 30 having an exhaust vent (not numbered) is coupled to an opening in patient sealing assembly 28 to allow the flow of breathing gas from pressure generating device 4 to be communicated to an interior space defined by patient sealing assembly 28, and then to the airway of a patient. Patient interface device 14 also includes a headgear component 32 for securing patient sealing assembly 28 to the head of patient 10. It will be understood that the patient interface device 14 described herein is meant to be exemplary only, and that other arrangements are also possible without varying from the scope of the present invention.

[0047] In the illustrated, non-limiting exemplary embodiment of the present invention, airway pressure support system 2 essentially functions as a pressure support system, and, therefore, includes all of the capabilities necessary in such systems in order to provide appropriate pressure levels to patient 10. This includes receiving the necessary parameters, via input commands, signals, instructions or other information, for providing appropriate pressure, such as maximum and minimum pressure settings. It should be understood that this is meant to be exemplary only, and that other pressure support methodologies, including, but not limited to, CPAP, BiPAP AutoSV, AVAPS, Auto CPAP, and BiPAP Auto, are within the scope of the present invention.

[0048] FIG. 3 is a flowchart showing a method 100 that may be implemented in conjunction with pressure support system 2 for concurrently stabilizing the airway of patient 10 (e.g., without limitation, such as for treating OSA) while also treating hypertension. Method 100 begins at step 102, when patient 10 begins their CPAP therapy such as by securing patient interface device 14 on their head and powering up/starting pressure generating device 4. Next, as shown at step 104, a flow of treatment gas is provided (e.g., via pressure generating device 4 of FIG. 1) to the patient in accordance with a first set of flow parameters. In an example embodiment utilizing the system 2 such as shown in FIG. 1, pressure generating device 4 is operated in a “default CPAP mode”. If auto titrating, then EPAP is adjusted by pressure generating device 4 as needed until airway patency is achieved. As shown in step 106, the flow of breathing gas is provided in accordance with the first set of flow parameters (e.g., in default CPAP mode) until it is determined that the patient has achieved stable breathing. Such determination may be made by considering one or more of several characteristics of the patient's breathing. For example, consistent minute ventilation (MV), breath rate (BR), tidal volume (TV), and/or lung compliance may be used to indicate that stable breathing has been achieved. It is to be appreciated that mechanisms and methods for determining and analyzing such characteristics are well known in the art and may be utilized without varying from the scope of the present invention. Accordingly, a detailed description of such mechanisms/techniques has not been provided herein.

[0049] Once it is determined at step 106 that the patient has achieved stable breathing, the method moves on to step 108 where lung hyper-ventilation mode is initiated. Next, as an initial step of hyper-ventilation mode, breath data (e.g., MV, BR, TV, LC) is collected at step 110 from which target patient breath parameters are then calculated, such as shown at step 112. As previously discussed, in order to effectively activate the patient's pulmonary stretch receptors, the patient's lungs generally need to be inflated beyond the threshold of a typical breath. Accordingly, the target patient breath parameters aim to inflate the lungs of the patient by an additional 50-400% of nominal tidal volume. For example, in one embodiment in which target TV is 200% of baseline TV, the target BR is approximately 50% of the baseline BR, so as to generally maintain the patient's MV. The collection of patient breath data at step 110 typically occurs over a few minutes, although such time may be varied without varying from the scope of the present invention. It is to be appreciated that mechanisms and methods for collecting and analyzing patient breath data (e.g., via pressure generating device 4) are well known in the art and may be utilized without varying from the scope of the present invention. Accordingly, a detailed description of such mechanisms/techniques has not been provided herein.

[0050] After the patient breath data has been collected at step 110 and target patient breath parameters are calculated/determined therefrom at step 112, the flow of breathing gas (e.g., the inspiratory positive airway pressure (IPAP) provided by pressure generating device 4) is adjusted (e.g., by controller 22) to a different set of flow parameters to attempt to bring the patient's breath (i.e., patient breath data) into accordance with the target patient breath parameters previously calculated in step 112. Such adjustment may be carried out: gradually over a predetermined period of time (e.g., without limitation, a few minutes); gradually over a predetermined number of breaths (e.g., without limitation 10 breaths); abruptly; or via any other timing or event arrangement (e.g., without limitation, receiving a signal from an external sensor that the patient is asleep).

[0051] After the flow of breathing gas has been adjusted to the different set of flow parameters, the patient's breathing is monitored so as to obtain new breath data, such as show at step 115. If from such monitoring it is determined, at step 116, that the new patient breath data accords with the target patient breathing parameters, the method moves on to step 117, wherein the patient is continued to be provided with the flow of treatment gas in accordance with the different set of flow parameters. However, if at step 116 it is determined that the patient's breath data, as monitored at step 115, does not accord with the target patient breath parameters, the method returns to step 114 and the flow of treatment gas to the patient is adjusted to yet another different set of flow parameters to try to bring the patient's breathing into accord with the target patient breath parameters.

[0052] While the flow of breathing gas is continued to be provided to the patient in accordance with the different set of flow parameters, such as shown at step 117, the occurrence/presence of one or more stop “stop conditions” is monitored, such as shown at step 118. The flow of treatment gas in accordance with the different set of flow parameters is continued to be provided to the patient until it is determined, at step 120, that a stop condition has occurred. As used herein, the term “stop condition”, refers to any condition which indicates that pressure generating device 4 is to cease operating in hyper-ventilation mode and either return to the operating mode prior to hyper-ventilation mode (i.e., provide the flow of treatment gas in accordance with the first set of flow parameters) or to power off. For example, in order to avoid causing a central apnea in the patient, the patient's breath tail could be monitored. If the breath tail exceeds a predetermined length of time (e.g., 8 seconds) a stop condition could be indicated and pressure generating device would discontinue hyper-ventilation mode and return to normal operation. Other examples of such stop conditions include, without limitation, a breathing instability (e.g., variable breathing, dsynchronous breaths) and changes in lung compliance (LC) which would potentially indicate that the patient is fighting treatment, and an indication that the treatment is disturbing the patient (e.g., causing restlessness, etc.). In the case of LC, as LC is the ratio of tidal volume to pressure support (i.e. IPAP-EPAP), as the IPAP is increased to achieve the target breath parameters (e.g. tidal volume) the ratio of tidal volume to pressure support is monitored. If this ratio starts to change (e.g. decrease) it means that the tidal volume that is achieved with a given amount of pressure support has decreased (i.e. the patient's body is resisting what the device is trying to do) which could be a sign that the patient is fighting the device or could be a sign that the patient's lungs are over-inflated. In addition to the aforementioned conditions, the passage of a predetermined amount of time could signify a stop event. For example, it may be desirable for a patient to only receive hyper-ventilation treatment for a portion of the time that a CPAP treatment is provided.

[0053] Once it has been determined at step 120 that a stop condition has occurred (and not a power off indication), hyper-ventilation mode ceases and the flow of treatment gas is provided to the patient in accordance with the first set of parameters (e.g., default CPAP mode), such as shown at step 122. Such transition from hyper-ventilation mode back to the first set of parameters may be abrupt (e.g., in an emergency) or may be gradual (e.g., to not disrupt a patient's sleep). The flow of breathing gas is provided in accordance with the first set of parameters until it is determined at step 124 that the stop condition previously determined at step 120 has ceased. Then, at step 126, if it is determined that the patient has once again achieved stable breathing, method 100 returns to step 117 and the patient is once again provided with the flow of breathing gas in accordance with the different set of flow parameters. However, if it is determined at step 126 that the patient has not achieved stable breathing, the flow of breathing gas is continued to be supplied in accordance with the first set of parameters.

[0054] FIG. 4 is a flowchart showing another method 200 that may be implemented in conjunction with pressure support system 2 for concurrently stabilizing the airway of patient 10 (e.g., without limitation, such as for treating OSA) while also treating hypertension. Similar to method 100, method 200 utilizes an increase in the flow of treatment gas beyond regular treatment levels to activate pulmonary stretch receptors. However, unlike method 100 which only increases the flow a single predetermined amount, method 200 carefully increases the flow incrementally without a predetermined maximum (aside from a potential safety ceiling). By safely increasing the flow beyond a predetermined set point, method 200 maximizes the effective treatment. When combined with an adaptive treatment for sleep apnea such as Auto CPAP, it should be understood that control schemas for both therapies (lung hyperinflation and Auto CPAP) can run in parallel with the Auto CPAP controller automatically titrating the EPAP to achieve an open and stable airway while the lung hyperinflation controller automatically titrates pressure support (IPAP-EPAP) to increase tidal volume flow.

[0055] Method 200 begins at step 202, when patient 10 begins their CPAP therapy such as by securing patient interface device 14 on their head and powering up/starting pressure generating device 4. Next, as shown at step 204, a flow of treatment gas is provided (e.g., via pressure generating device 4 of FIG. 1) to the patient in accordance with an initial set of flow parameters. In an example embodiment utilizing the system 2 such as shown in FIG. 1, pressure generating device 4 is operated in a “default CPAP mode”. If auto titrating, then EPAP is adjusted by pressure generating device 4 as needed until airway patency is achieved. The flow of breathing gas is provided in accordance with the initial set of flow parameters (e.g., in default CPAP mode) until it is determined, at step 206, that one or more initial condition(s) of the patient have been met. Such initial condition(s) may include, for example without limitation, stable breathing by the patient. Stable breathing may be determined by considering one or more of several characteristics of the patient's breathing. For example, consistent minute ventilation (MV), breath rate (BR), tidal volume (TV), and/or lung compliance may be used to indicate that stable breathing has been achieved. Also, stable breathing is achieved when there are no sleep-disordered breathing events (e.g. apnea, hypopnea, periodic breathing, or respiratory effort-related arousal). It is to be appreciated that mechanisms and methods for determining and analyzing such characteristics are well known in the art and may be utilized without varying from the scope of the present invention. Accordingly, a detailed description of such mechanisms/techniques has not been provided herein. Such initial condition(s) may also include determining sleep onset by the patient which may be carried out via any suitable means.

[0056] Once it is determined at step 206 that the initial condition(s) have been met, the method moves on to step 208 where lung hyper-ventilation (HV) mode is initiated. Next, as initial steps of hyper-ventilation mode: an overall timer which records the time spent in hyper-ventilation mode is started (from zero), as shown in step 210 and the flow parameters are increased by a predetermined amount, as shown in step 212. Such predetermined amount is typically in the range of 0.5-2.0 cmH2O, although other amounts may be employed without varying form the scope of the present invention. Such amount could be determined by a default value, adjustable machine setting, current amount of pressure support (e.g. could increase pressure support more aggressively at the beginning and then increase it more slowly as it approaches the max pressure support). Also, the amount could be based on previous nights' experience (e.g. it could step more aggressively up to a level, or near a level, that the patient has successfully achieved on previous nights).

[0057] As further initial steps of hyper-ventilation mode: a stop condition (SC) counter is set to zero, as shown in step 214; a sub-timer is set to zero and started, as shown in step 216; and the flow of breathing gas is provided to the patient in accordance with the increased flow parameters (i.e., increased from the initial flow parameters), as shown in step 220. Although described in a particular order, it is to be appreciated that steps 210-220 are carried out in a very short timeframe and may generally be carried out in any order and/or carried out concurrently without varying from the scope of the present invention. It is also to be appreciated that the increase in flow of breathing gas to the patient may be carried out: gradually over a predetermined period of time (e.g., without limitation, a few minutes); gradually over a predetermined number of breaths (e.g., without limitation 10 breaths); abruptly; or via any other timing or event arrangement (e.g., without limitation, receiving a signal from an external sensor that the patient is asleep), preferably in a manner which is most comfortable to the patient and which does not interrupt sleep.

[0058] While the flow of breathing gas is provided to the patient in accordance with the increased flow parameters, such as shown at step 220, the occurrence/presence of one or more stop “stop conditions” (SC) is monitored while the flow of treatment gas is continued to be provided to the patient in accordance with the increased set of flow parameters until one of two potential events occurs: i) it is determined at step 222 that a stop condition (such as previously discussed in regard to FIG. 3) has occurred; or ii) it is determined at step 226 that the sub-timer has reached a predetermined time (e.g., without limitation, 1-10 minutes). As an alternative to using a period of time, a particular number of breaths (e.g., without limitation, 10 breaths) may be used.

[0059] If at step 222 it is determined that a stop condition has occurred, the stop condition counter is incremented in step 228, the flow parameters are decreased by a predetermined amount (e.g., without limitation, by 0.5-1.0 cmH2O or other suitable amount) as shown in step 230, and the flow of treatment gas is provided to the patient in accordance with the decreased flow parameters, as shown in step 232. Such transition of the flow to the decreased flow parameters may be abrupt or may be gradual (e.g., to not disrupt a patient's sleep). As shown in step 236, while receiving treatment gas in accordance with the reduced flow parameters, the patient is monitored for the presence of a stop condition and if it is determined that the stop condition is still present, then the method loops back to steps 230 and 232 where the flow parameters are further decreased by a predetermined amount and the flow of treatment gas is provided to the patient in accordance with the (further) decreased flow parameters. Accordingly, steps 230 and 232 are repeated, and thus the flow of treatment gas provided to the patient is reduced, until it is determined at step 236 that the stop condition has ceased, and further in step 238 that initial conditions (e.g., the same or similar to those previously discussed in regard to step 206) have also been met. If at step 238 it is determined that initial condition have been met, the method then moves on to step 240 which will be discussed further below.

[0060] If it is determined at steps 222 and 226 that a stop condition has not occurred and that the sub-timer has reached a predetermined time (thus indicating the patient has received the elevated level of treatment gas for a predetermined time), the method then proceeds to step 240.

[0061] In step 240, a determination is made as to whether a stop increasing indicator has occurred and/or is present. Such stop increasing indicator signifies that no further increases to the flow parameters should be made. Such a stop increasing indicator may be a threshold indicating that stop conditions have been met. For example, such threshold may indicate that attempts have been made to increase the pressure support a certain amount of times and such increase causes a stop condition each time. As another example, such stop increasing indicator could be a maximum pressure support threshold based on safety and machine capabilities that should not be exceeded. As yet another example, such stop increasing indicator could be a maximum hyperinflation threshold based on efficacious range (e.g. 400%) that should not be exceeded. If it is determined in step 240 that no stop increasing indicator has occurred and/or is present, the method returns to step 212 where the flow parameters are once again increased and the method progresses to 214 and beyond as previously discussed.

[0062] Conversely, if it is determined in step 240 that a stop increasing indicator has occurred and/or is present, the method moves on to step 242 where the a determination is made as to whether or not an exit hyper-ventilation mode indicator has occurred and/or is present. Such exit hyper-ventilation mode indicator signifies that the system should end hyper-ventilation mode and return to regular therapy mode. Such exit hyper-ventilation mode indicator may include, for example, without limitation, one or more of: the overall timer reaching a predetermined amount (e.g., without limitation, a time in the range of several minutes to hours), thus indicating the hyper-ventilation treatment session has been provided for a desired treatment time; the stop condition counter has reached a predetermined count, thus indicating that the patient has exhibited a predetermined maximum safe number of stop conditions; or other desired indicator.

[0063] If it is determined in step 242 that no exit hyper-ventilation mode indicator has occurred and/or is present, the method returns to step 220 where patient is provided the flow of treatment gas in accordance with the flow parameters are once again increased and the method progresses to 214 and beyond as previously discussed.

[0064] Conversely, if it is determined in step 242 that an exit hyper-ventilation mode indicator has occurred and/or is present, the method moves on to step 244 where hyper-ventilation mode is exited, and then onto step 246 where the patient is once again provided with the flow of treatment gas in accordance with the initial set of flow parameters (similar to step 204) until the therapy session ends (e.g., when the patient wakes in the morning) such as shown in step 248.

[0065] From the foregoing description it is to be appreciated that the present invention provides for the combined treatment of both OSA and hypertension with a single respiratory therapy mode. It is also to be appreciated that such approach ensures that patient physiology is not adversely affected by lung-hyperventilation and ensures that patient comfort is maintained.

[0066] In the claims, any reference signs placed between parentheses shall not be construed as limiting the claim. The word “comprising” or “including” does not exclude the presence of elements or steps other than those listed in a claim. In a device claim enumerating several means, several of these means may be embodied by one and the same item of hardware. The word “a” or “an” preceding an element does not exclude the presence of a plurality of such elements. In any device claim enumerating several means, several of these means may be embodied by one and the same item of hardware. The mere fact that certain elements are recited in mutually different dependent claims does not indicate that these elements cannot be used in combination.

[0067] Although the invention has been described in detail for the purpose of illustration based on what is currently considered to be the most practical and preferred embodiments, it is to be understood that such detail is solely for that purpose and that the invention is not limited to the disclosed embodiments, but, on the contrary, is intended to cover modifications and equivalent arrangements that are within the spirit and scope of the appended claims. For example, it is to be understood that the present invention contemplates that, to the extent possible, one or more features of any embodiment can be combined with one or more features of any other embodiment.