Exhaled gas measurement compensation during high flow respiratory therapy
US-2024398255-A1 · Dec 5, 2024 · US
US9931484B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9931484-B2 |
| Application number | US-201013319113-A |
| Country | US |
| Kind code | B2 |
| Filing date | May 11, 2010 |
| Priority date | Jun 9, 2009 |
| Publication date | Apr 3, 2018 |
| Grant date | Apr 3, 2018 |
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An interface appliance is configured to deliver a flow of fluid to the airway of a subject. The generation of the flow of fluid may be controlled to provide a therapeutic benefit to the subject. The interface appliance is configured to carry one or more sensors ( 24 ) configured to detect one or more parameters related to the flow of fluid on the subject. The one or more parameters may then be used to control the generation and/or delivery of the flow of fluid.
Opening claim text (preview).
The invention claimed is: 1. A system configured to measure one or more parameters, the system comprising: a nasal cannula comprising a main conduit, a pair of sleeves, a protrusion, and a pair of hollow prongs that extend from the main conduit, wherein the hollow prongs are configured to be inserted into the nostrils of a subject such that a flow of fluid in the main conduit is communicated to the nostrils of the subject through the hollow prongs, the pair of sleeves extend from the main conduit adjacent to the pair of hollow prongs such that a first sleeve is formed integrally with one of the hollow prongs, and a second sleeve is formed by the protrusion, wherein the pair of sleeves, the one of the hollow prongs, and a portion of the main conduit are a monolithic part in the nasal cannula, the protrusion extending away from the main conduit such that during use of the nasal cannula, the first sleeve is inserted in one of the nostrils of the subject and the second sleeve is outside of the one of the nostrils of the subject; and a base removably received by the main conduit of the nasal cannula, the base comprising: one or more sensors disposed on the base such that at least a portion of the one or more sensors is disposed on or directly adjacent to at least one of the hollow prongs, the one or more sensors being configured to generate one or more output signals that convey information related to at least one parameter related to the flow of fluid between the nostrils of the subject and the nasal cannula; wherein the at least one parameter is associated with pulse oximetry, and wherein the one or more sensors comprise a pulse oximeter, the pulse oximeter comprising: an electromagnetic radiation source configured to emit electromagnetic radiation incident on a wall of one of the nostrils of the subject responsive to the hollow prongs being inserted into the nostrils of the subject; and a photosensitive detector configured to receive a portion of the electromagnetic radiation emitted by the electromagnetic radiation source that propagates through the wall of the nostril; wherein the electromagnetic radiation source and the photosensitive detector are configured to be positioned on an inner nostril wall and an outer nostril wall located on the exterior surface of the nose of the subject during use of the nasal cannula; and a first electronic interface disposed on a coupling portion of the base in electronic contact with a corresponding second electronic interface disposed on the nasal cannula between the pair of sleeves, wherein the one or more output signals generated by the one or more sensors are output via the first electronic interface. 2. The system of claim 1 , further comprising: a pressure generator configured to generate a flow of fluid; and wherein a processor is configured to control the pressure generator such that one or more gas parameters of the gas in the flow of fluid is controlled in a feedback manner based on the one or more output signals of the one or more sensors. 3. The system of claim 1 , wherein the at least one parameter further comprises the flow rate within the nasal cannula. 4. The system of claim 1 , wherein the base is removable from the nasal cannula such that the base can be reused with another nasal cannula. 5. The system of claim 1 , wherein the base is generally U-shaped including a first distal end, and a second distal end, such that the first distal end is in contact with the first sleeve and the second distal end is in contact with the second sleeve, and wherein the first electronic interface is disposed on the coupling portion of the base. 6. The system of claim 1 , wherein the at least one parameter further comprises one or more physiological parameters of the subject. 7. The system of claim 6 , wherein the first electronic interface includes one or more wireless transmitters and or receivers to communicate the output signals wirelessly. 8. A method of determining a parameter with a nasal cannula comprising a main conduit; a pair of hollow prongs configured to be inserted into the nostrils of a subject; a protrusion; and a pair of sleeves extending from the main conduit such that a first sleeve is formed integrally with one of the hollow prongs, and a second sleeve is formed by the protrusion, wherein the pair of sleeves, the one of the hollow prongs, and a portion of the main conduit are a monolithic part in the nasal cannula, the protrusion extending away from the main conduit such that during use of the nasal cannula, the first sleeve is inserted in one of the nostrils of the subject a protrusion and the second sleeve is outside of the one of the nostrils, the method comprising: communicating a flow of fluid with the nostrils of the subject through the nasal cannula; generating one or more output signals that convey information related to at least one parameter related to the flow of fluid between the nostrils of the subject and the nasal cannula, wherein the one or more output signals are generated by one or more sensors disposed on a base such that at least a portion of the one or more sensors is disposed on or directly adjacent to at least one of the hollow prongs; wherein the at least one parameter is associated with pulse oximetry, and wherein generating one or more output signals that convey information related to the at least one parameter comprises: emitting electromagnetic radiation onto a wall of one of the nostrils of the subject; receiving a portion of the electromagnetic radiation emitted by the electromagnetic radiation source that propagates through the wall of the nostril; and generating an output signal that conveys information related to one or more radiation parameters of the received electromagnetic radiation; wherein the electromagnetic radiation source and the photosensitive detector are configured to be positioned on an inner nostril wall and an outer nostril wall located on the exterior surface of the nose of the subject during use of the nasal cannula; and communicating the one or more output signals generated by the one or more sensors via a first electronic interface disposed on the base, wherein the first electronic interface is in electronic contact with a corresponding second electronic interface disposed on the nasal cannula between. 9. The method of claim 8 , further comprising: generating the flow of fluid; and controlling one or more aspects of the generation of the flow of fluid in a feedback manner based on the one or more output signals of the one or more sensors. 10. The method of claim 8 , wherein the at least one parameter further comprises the flow rate of gas within the nasal cannula. 11. The method of claim 8 , wherein the base is removable from the nasal cannula such that the base can be reused with another nasal cannula. 12. The method of claim 8 , wherein the base is generally U-shaped including a first distal end, a second distal end, and a coupling portion such that the first distal end is in contact with the first sleeve and the second distal end is in contact with the second sleeve, and wherein the first electronic interface is disposed on the coupling portion of the base. 13. The method of claim 8 , wherein the at least one parameter further comprises one or more physiological parameters of the subject. 14. The method of claim 13 , further comprising wirelessly communicating the output signals generated by the one or more sensors via the first electronic interface wherein the first electronic interface includes one or more wireless transmitters and or receivers. 15. A system configured to determine a parameter, the
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used specific wavelengths · CPC title
with microprocessors or computers · CPC title
in the breathing tube and used in both inspiratory and expiratory phase · CPC title
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