System and Method for Improved Treatment of Sleeping Disorders using Therapeutic Positive Airway Pressure
Abstract
Described is a method and system providing therapeutic positive airway pressure to a particular area of patient's airways. The system may include a flow generator and a processing arrangement. The flow generator supplies an airflow to an airway of the patient. The processing arrangement is connected to the flow generator to control a supply pressure at which the airflow is generated by the flow generator. The processing arrangement continuously adjusts the supply pressure to maintain a pressure in a predetermined portion of the patient's airway substantially constant. The predetermined portion of the patient's airway includes a collapsible portion of an upper airway of the patient. The processing arrangement also controls the supply pressure to maintain the pressure in the collapsible portion of the patient's airway at a value at least as great as a tissue pressure below which the collapsible portion collapses.
Claims
exact text as granted — not AI-modified1 - 22 . (canceled)
23 . A device for treatment of a sleeping disorder, comprising:
a flow generator configured to supply air to an airway of a patient at a predetermined pressure P A ; a processing arrangement operably connected to the flow generator to maintain a gas pressure within a predetermined portion of the patient's airway within a desired range by adjusting one or both of the rate of airflow and a pressure supplied by the flow generator.
24 . The device of claim 23 , wherein the processing arrangement is configured to maintain a substantially constant pressure C P within the patient's airway, the pressure C P being selected to prevent a collapse of the patient's airway.
25 . The device of claim 24 , further comprising a mask connected to the tube and configured to connect the flow generator to the airway of the patient.
26 . The device of claim 25 , further comprising a flow tube extending from the flow generator to the airway of the patient, the flow tube having a resistance R AB , wherein the value R AB is measured when the flow generator is providing the airflow and the mask is open to the atmosphere.
27 . The device of claim 26 , wherein the flow generator is configured to provide the airflow at one of a constant and a variable flow rate.
28 . The device of claim 26 , wherein the pressure P A may be continuously adjusted according to the formula: P A =C P +R AB *F S +R BC *Fp, wherein:
R BC is a resistance in the predetermined portion of the patient's airway; F s is an instantaneous rate of flow of air flowing from the flow generator to the patient; F p is an instantaneous rate of flow of air via inhalation and exhalation of the patient; wherein the values of F S and F P are negative during expiration and positive during inspiration.
29 . The device of claim 26 , wherein the pressure P A is continuously adjusted according to R AB and R BC , wherein R BC is a resistance in the predetermined portion of the patient's airway.
30 . The device of claim 28 , wherein the value of R BC may be determined from one of (a) a resistance measured from the patient, (b) a fixed standardized resistance, (c) a resistance based on a rhinometric analysis of the patient and (d) an estimated resistance based on a pathology of the patient's nose.
31 . The device of claim 29 , wherein the value of R BC may be determined from one of (a) a resistance measured from the patient, (b) a fixed standardized resistance, (c) a resistance based on a rhinometric analysis of the patient and (d) an estimated resistance based on a pathology of the patient's nose.
32 . The device of claim 24 , wherein the pressure C P is maintained substantially constant throughout one of an entire inspiratory phase and a full respiratory cycle.
33 . The device of claim 32 , wherein the pressure C P applied during the expiratory phase is lower than the pressure C P applied during the inspiratory phase.
34 . The device of claim 23 , further comprising a venting arrangement configured to prevent the patient from rebreathing exhaled gases.
35 . The device of claim 34 , wherein the venting arrangement is one of a leak port or a non-rebreathing valve.
36 . The device of claim 34 , wherein the venting arrangement vents the exhaled gas to the atmosphere.
37 . The device of claim 28 , further comprising a first pressure sensor coupled to the flow tube and configured to measure a pressure within the flow tube and provide the measured data to the processing arrangement.
38 . The device of claim 37 , further comprising a second pressure sensor configured to measure a pressure in one of the mask and the flow generator and provide the measured data to the processing arrangement.
39 . The device of claim 23 , wherein the predetermined portion of the patient's airway is a portion of the upper airway susceptible to collapse.
40 . A method for treating a sleeping disorder, comprising the steps of:
supplying an airflow to an airway of a patient at a predetermined pressure P A ; and maintaining a gas pressure within a predetermined portion of the patient's airway within a desired range by adjusting one or both of the rate of airflow and a pressure supplied by the flow generator via a processing arrangement operably connected to a flow generator.
41 . The method according to claim 40 , wherein the processing arrangement is configured to maintain a substantially constant pressure C P within the patient's airway, the pressure C P being selected to prevent a collapse of the patient's airway.
42 . The method according to claim 41 , wherein the pressure C P is maintained substantially constant in the predetermined portion throughout one of an entire inspiratory phase and a full respiratory cycle.
43 . The method according to claim 41 , further comprising the steps of:
generating the airflow using the flow generator, the flow generator being coupled to the patient's airway by a flow tube; and providing the airflow to a mask situated over at least one of a nose and a mouth of the patient via the flow tube.
44 . The method according to claim 40 , further comprising the step of:
diverting, via a venting arrangement, gases exhaled by the patient from an incoming airflow to prevent re-breathing of the exhaled gases.
45 . The method according to claim 43 , further comprising the step of:
determining a supply pressure P A according to the following formula:
P A =C P +R AB *Fs+R BC *F P
wherein, P A is the supply pressure provided by the flow generator; R AB is a resistance in the flow tube, wherein the value R AB is measured when the flow generator is providing the airflow and the mask is opened to the atmosphere; F s is an instantaneous rate of flow of air flowing from the flow generator to the patient; R BC is a resistance in the predetermined portion of the patient's airway, wherein the value of R BC may be determined from one of (a) a resistance measured from the patient, (b) a fixed standardized resistance, (c) a resistance based on a rhinometric analysis of the patient and (d) an estimated resistance based on a pathology of the patient's nose; and F P is an instantaneous rate of flow of air via inhalation and exhalation of the patient, wherein the values of F S and F P are negative during expiration and positive during inspiration.
46 . The method according to claim 45 , further comprising the steps of:
measuring, via a first sensor, a first value of pressure in the flow tube; and providing the measured data to the processing arrangement.
47 . The method according to claim 46 , further comprising the steps of:
measuring, via a second sensor, a second value of pressure within one of the flow generator and the mask; and providing the measured data to the processing arrangement.Cited by (0)
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