Acoustic damping for blower in cpap device / pap device with noise reducing enclosure
US-2017182270-A1 · Jun 29, 2017 · US
US11278698B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-11278698-B2 |
| Application number | US-201515122951-A |
| Country | US |
| Kind code | B2 |
| Filing date | Feb 4, 2015 |
| Priority date | Mar 4, 2014 |
| Publication date | Mar 22, 2022 |
| Grant date | Mar 22, 2022 |
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The present disclosure pertains to a system configured to amplify the pressure and/or flow rate of a pressurized flow of breathable gas by entraining oxygen gas and/or ambient air with an air amplifier and a venturi valve at or near a blending gas source, distally (e.g., remotely) from an interface appliance of a subject interface (e.g., away from the face of the subject) to reduce noise from the system heard by the subject. The system is configured to provide this pressure support and/or ventilation with oxygen therapy. The system is configured to deliver ventilatory and/or pressure support with oxygen therapy while decreasing output requirements of the blending gas source and/or pressure generator.
Opening claim text (preview).
The invention claimed is: 1. A system configured to deliver a blending gas enriched pressurized flow of breathable gas to the airway of a subject, the system comprising: a pressure generator configured to generate compressed gas; a blending gas source configured to provide blending gas; an air amplifier configured to receive the compressed gas from the pressure generator and the blending gas from the blending gas source into the pressurized flow of breathable gas, and amplify a pressure of the pressurized flow of breathable gas that includes the blending gas; a venturi valve configured to receive the pressurized flow of breathable gas from the air amplifier and entrain ambient air into the pressurized flow of breathable gas during inhalation of the subject; an interface appliance coupled to, and in direct communication with, the venturi valve by a flexible conduit, the interface appliance being configured to communicate the pressurized flow of breathable gas communicated from the venturi valve via the conduit to the airway of the subject; one or more sensors configured to generate output signals conveying information related to one or more gas parameters of the pressurized flow of breathable gas; and one or more physical computer processors configured by computer readable instructions to control the pressure generator, the blending gas source, and the air amplifier to deliver the pressurized flow of breathable gas to the subject according to a bi-level positive pressure support therapy regime based on the output signals, wherein the pressure generator, the blending gas source, the air amplifier, and the venturi valve are provided in a grouping located remotely from the interface appliance to reduce noise from the pressure generator, the blending gas source, the air amplifier, and/or the venturi valve heard by the subject. 2. The system of claim 1 , wherein the blending gas source is configured such that the blending gas is oxygen, and wherein the blending gas source is an oxygen concentrator, bottled compressed oxygen, or liquid oxygen. 3. The system of claim 1 , wherein the one or more physical computer processors are configured such that controlling the pressure generator, the blending gas source, and the air amplifier to deliver the pressurized flow of breathable gas to the subject according to the bi-level positive pressure support therapy regime includes: determining inhalation phases and/or exhalation phases during breathing of the subject based on the output signals; controlling the pressure generator to adjust a positive end expiratory pressure in the subject based on the output signals, the inhalation and/or exhalation phase determinations, and the bi-level pressure support therapy regime; and controlling the blending gas source to adjust an amount of the blending gas in the pressurized flow of breathable gas based on the output signals, the inhalation and/or exhalation phase determinations, and the bi-level pressure support therapy regime. 4. The system of claim 1 , wherein the grouping is positioned within a portable bag while the blending gas enriched pressurized flow of breathable gas is delivered to the airway of the subject. 5. The system of claim 4 , wherein the portable bag is structured to be carried on the subject while the blending gas enriched pressurized flow of breathable gas is delivered to the airway of the subject. 6. The system of claim 4 wherein the portable bag is structured to be carried on the subject about the hips of the subject while the blending gas enriched pressurized flow of breathable gas is delivered to the airway of the subject. 7. The system of claim 1 , wherein the interface appliance comprises one of: a nasal cannula, a nasal mask, a nasal/oral mask, a full face mask, or a total face mask. 8. A method for delivering a blending gas enriched pressurized flow of breathable gas with a delivery system, the system comprising: a pressure generator, a blending gas source, an air amplifier, one or more sensors, one or more physical computer processors, a venturi valve, a flexible conduit, and an interface appliance configured to communicate the pressurized flow of breathable gas to the airway of the subject, the method comprising: locating the pressure generator, the blending gas source, the air amplifier, and the venturi valve in a grouping remote from the interface appliance to reduce noise from the pressure generator, the blending gas source, the air amplifier, and/or the venturi valve heard by the subject; coupling the pressure generator, the blending gas source, the air amplifier, and the venturi valve with the interface appliance via the flexible conduit, with the venturi valve being in direct communication with the interface appliance; generating compressed gas with the pressure generator; providing blending gas with the blending gas source; receiving the compressed gas from the pressure generator with the air amplifier; receiving the blending gas from the blending gas source with the air amplifier; amplifying a pressure of the pressurized flow of breathable gas that includes the blending gas with the air amplifier; receiving, with the venturi valve, the pressurized flow of breathable gas from the air amplifier and entraining ambient air into the pressurized flow of breathable gas during inhalation of the subject; generating, with the one or more sensors, output signals conveying information related to one or more gas parameters of the pressurized flow of breathable gas; and controlling, with the one or more physical computer processors, the pressure generator, the blending gas source, and the air amplifier to deliver the pressurized flow of breathable gas to the subject according to a bi-level positive pressure support therapy regime based on the output signals. 9. The method of claim 8 , wherein the blending gas is oxygen, and wherein the blending gas source is an oxygen concentrator, bottled compressed oxygen, or liquid oxygen. 10. The method of claim 8 , wherein controlling the pressure generator, the blending gas source, and the air amplifier to deliver the pressurized flow of breathable gas to the subject according to the bi-level positive pressure support therapy regime includes: determining inhalation phases and/or exhalation phases during breathing of the subject based on the output signals; controlling the pressure generator to adjust a positive end expiratory pressure in the subject based on the output signals, the inhalation and/or exhalation phase determinations, and the bi-level pressure support therapy regime; and controlling the blending gas source to adjust an amount of the blending gas in the pressurized flow of breathable gas based on the output signals, the inhalation and/or exhalation phase determinations, and the bi-level pressure support therapy regime. 11. The method of claim 8 , wherein the grouping is positioned within a portable bag while the pressurized flow of breathable gas is delivered to the subject.
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