Acclimization therapy for first time CPAP and NIV users

US11730906B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-11730906-B2
Application numberUS-202017038039-A
CountryUS
Kind codeB2
Filing dateSep 30, 2020
Priority dateJun 14, 2005
Publication dateAug 22, 2023
Grant dateAug 22, 2023

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  1. Title

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  2. Abstract

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  3. Assignees and inventors

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  4. Key dates

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  5. First independent claim

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  6. CPC / IPC classifications

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  7. Citations and related patents

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Abstract

Official abstract text for this publication.

A method of acclimatizing a patient to provide continuous positive airway pressure (CPAP) therapy, including operating a device for treating sleep disordered breathing (SDB). The device provides continuous positive airway pressure to the patient during sleep via a mask configured to provide a seal with respect to airways of the patient. The method comprises applying full therapeutic pressure during a first session, monitoring a mask pressure during application of the full therapeutic pressure, calculating a difference between the full therapeutic pressure and the mask pressure, comparing the difference to a threshold representing an acceptable level of leak, generating a first signal in response to said comparing, and in response to said first signal indicating a fault in the seal, decreasing an applied pressure to below the full therapeutic pressure during the first session in order to improve the seal of the mask against the patient's face.

First claim

Opening claim text (preview).

The invention claimed is: 1. A method of acclimatizing a patient to provide continuous positive airway pressure (CPAP) therapy, including operating a device comprising a blower and a controller for treating sleep disordered breathing (SDB), wherein said device provides continuous positive airway pressure to the patient during sleep via a mask configured to provide a seal with respect to airways of the patient, the method comprising: applying therapeutic pressure at a first therapeutic pressure during a treatment session; monitoring a mask pressure within the mask during application of the first therapeutic pressure; calculating a difference between the first therapeutic pressure and the mask pressure; comparing the difference to a first threshold representing an acceptable level of leak; generating a first signal in response to said comparing and indicative of performance of the seal; in response to said first signal indicating a fault in the seal, increasing the applied therapeutic pressure above the first therapeutic pressure during the treatment session; and based on a difference between the mask pressure at the applied first therapeutic pressure and the mask pressure at the applied increased therapeutic pressure being less than a second threshold, decreasing the applied therapeutic pressure to below the first therapeutic pressure during the treatment session in order to improve the seal of the mask against the patient's face. 2. The method according to claim 1 , the method further comprising maintaining the applied pressure below the first therapeutic pressure for a predetermined period of time, and returning the applied pressure to the first therapeutic pressure during the treatment session after the predetermined period of time has elapsed. 3. The method according to claim 2 , wherein the predetermined period of time is 15 minutes. 4. The method according to claim 2 , wherein the predetermined period of time is between 15-60 seconds. 5. The method according to claim 1 , wherein the applied pressure is maintained below the first therapeutic pressure for a remainder of the treatment session. 6. The method according to claim 1 , wherein the first threshold is static during the treatment session. 7. The method according claim 1 , wherein the first threshold fluctuates during the treatment session, and the first threshold is a function of a patient sleep phase indicator, a flow flattening indicator, a snoring indicator, apneas or hypopneas indicators, and/or an Apnea Hypopnea Index (AHI). 8. The method according to claim 1 , further comprising alerting the patient at a conclusion of the treatment session that the fault in the seal was detected. 9. The method according to claim 1 , further comprising: monitoring the mask pressure within the mask during application of the increased therapeutic pressure; calculating a difference between the mask pressure at the applied first therapeutic pressure and the mask pressure at the applied increased therapeutic pressure; based on the difference between the mask pressure at the applied first therapeutic pressure and the mask pressure at the applied increased therapeutic pressure being greater than the second threshold, continue applying the increased therapeutic pressure during the treatment session. 10. The method according to claim 1 , further comprising after decreasing the applied pressure to below the first therapeutic pressure, progressively increasing the applied pressure back up to the first therapeutic pressure based on detecting arousal of the patient. 11. A positive airway pressure (PAP) device comprising: a mask configured to seal against a patient's face; a blower configured to deliver pressurized air at a treatment pressure to the patient's airways via the mask; a controller in communication with the blower and configured to control the treatment pressure of the pressurized air, the controller configured to be programmed to cause the blower to deliver the pressurized air at an applied therapeutic pressure having a first therapeutic pressure during a treatment session; wherein, the controller is configured to: calculate a difference between the first therapeutic pressure and a mask pressure within the mask; compare the difference to a first threshold representing an acceptable level of leak; and in response to the difference being greater than the first threshold, cause the blower to deliver the pressurized air at a higher pressure above the first therapeutic pressure during the treatment session; and based on a difference between the mask pressure at the applied first therapeutic pressure and the mask pressure at the applied increased therapeutic pressure being less than a second threshold, cause the blower to deliver the pressurized air at a lower pressure below the first therapeutic pressure during the treatment session in order to improve the seal of the mask against the patient's face. 12. The PAP device according to claim 11 , wherein the controller is configured to: based on the difference between the mask pressure at the applied first therapeutic pressure and the mask pressure at the applied increased therapeutic pressure being greater than the second threshold, continue applying the increased therapeutic pressure during the treatment session. 13. The PAP device according to claim 11 , wherein the controller is configured to cause the blower to deliver the pressurized air at the lower pressure for a remainder of the treatment session. 14. The PAP device according to claim 11 , wherein the controller is configured to cause the blower to deliver the pressurized air at progressively increasing pressures until the treatment pressure has returned to the first therapeutic pressure during the treatment session. 15. The PAP device according to claim 14 , wherein the controller is configured to cause the blower to deliver the pressurized air at progressively increasing pressures after a predetermined period of time has elapsed. 16. The PAP device according to claim 15 , wherein the predetermined period of time is 15-60 seconds. 17. The PAP device according to claim 11 , wherein the controller is configured receive an input indicating a value for the first threshold, and the controller is configured to keep the value static during the treatment session. 18. The PAP device according to claim 11 , further comprising a sensor configured to monitor the patient's sleep phase and/or flow limitations in the patient's breathing, the controller configured to vary the first threshold during the treatment session based on the monitored sleep phase and/or flow limitations. 19. The PAP device according to claim 11 , wherein the controller is configured to alert the patient at a conclusion of the treatment session that a fault in the seal was detected. 20. The PAP device according to claim 11 , wherein the controller is configured to: calculate a differential between the treatment pressure at the lower pressure and the mask pressure within the mask when the blower is delivering the pressurized air at the lower pressure; compare the differential to the first threshold; and in response to the differential being less than the first threshold, cause the blower to deliver the pressurized air at progressively increasing pressures until the treatment pressure has returned to the first therapeutic pressure during the treatment session.

Assignees

Inventors

Classifications

  • with alarm devices · CPC title

  • Blowers or centrifugal pumps · CPC title

  • the speed thereof being controlled by respiratory parameters, e.g. by inhalation · CPC title

  • including calculation means, e.g. using a processor · CPC title

  • Respiratory or anaesthetic masks · CPC title

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What does patent US11730906B2 cover?
A method of acclimatizing a patient to provide continuous positive airway pressure (CPAP) therapy, including operating a device for treating sleep disordered breathing (SDB). The device provides continuous positive airway pressure to the patient during sleep via a mask configured to provide a seal with respect to airways of the patient. The method comprises applying full therapeutic pressure du…
Who is the assignee on this patent?
ResMed Pty Ltd
What technology area does this patent fall under?
Primary CPC classification A61M16/0051. Mapped technology areas include Human Necessities.
When was this patent published?
Publication date Tue Aug 22 2023 00:00:00 GMT+0000 (Coordinated Universal Time) (B2). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 3 related publications on this page (citations in our corpus or others sharing the same primary CPC).