# US 9,750,908 B2 · System, apparatus and methods for supplying gases

> Agents: this data is available as JSON from the patentgrep API and MCP server — see https://patentgrep.com/llms.txt

- Number: US 9,750,908 B2
- Document ID: US9750908B2
- Status: Granted
- Kind: B2
- Application number: 14/378,924
- Filed: 2013-02-15
- Published: 2016-01-21
- Granted: 2017-09-05
- Earliest claimed: 2012-02-15
- Assignees: Fisher & Paykel Healthcare Limited; New York University
- Applicants: Fisher & Paykel Healthcare Limited
- Inventors: Donald Roy Kuriger; David Cumin; David M. Rapoport; Christopher Earl Nightingale; Sujeewa Wannigama; Mark John Arrowsmith; Vitaly Kapelevich
- Web page: https://patentgrep.com/patent/US9750908B2

## CPC

- A61M 16/0069: {the speed thereof being controlled by respiratory parameters, e.g. by inhalation}
- A61B 5/4818: {Sleep apnoea}
- A61M 16/0051: {with alarm devices}
- A61M 16/06: Respiratory or anaesthetic masks
- A61M 16/1075: {by influencing the temperature (A61M16/1045 takes precedence)}
- A61M 16/109: {the humidifying liquid or the beneficial agent}
- A61M 16/16: Devices to humidify the respiration air {(A61M16/1045 takes precedence)}
- A61M 16/20: Valves specially adapted to medical respiratory devices
- A61M 16/202: {electrically actuated}
- A61M 16/204: {used for inhalation control}
- A61M 16/205: {used for exhalation control}
- A61M 16/208: {Non-controlled one-way valves, e.g. exhalation, check, pop-off non-rebreathing valves}
- A61M 16/22: Carbon dioxide-absorbing devices {; Other means for removing carbon dioxide}(cartridges with absorbing substances for respiratory apparatus A62B19/00)
- A61M 2016/0027: {pressure meter}
- A61M 2016/003: {with a flowmeter}
- A61M 2016/0039: {in the inspiratory circuit}
- A61M 2205/14: Detection of the presence or absence of a tube, a connector or a container in an apparatus
- A61M 2205/3303: Using a biosensor
- A61M 2205/3334: Measuring or controlling the flow rate
- A61M 2205/42: Reducing noise
- A61M 2205/50: with microprocessors or computers
- A61M 2205/6054: Magnetic identification systems
- A61M 2230/42: Rate
- A61M: DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY (introducing media into or onto the bodies of animals A61D7/00; means for inserting tampons A61F13/26; devices for administering food or medicines orally A61J; containers for collecting, storing or administering blood or medical fluids A61J1/05); DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY (surgery A61B; chemical aspects of surgical articles A61L); DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR {(Electrotherapy, e.g. producing anaesthesia by the use of alternating or intermittent currents A61N1/36021)}
- A61B: DIAGNOSIS; SURGERY; IDENTIFICATION (usefulness limited to only animals A61D)

## Abstract

A system, apparatus and methods are provided for supplying gases to a user. The supply includes a sub-therapeutic mode and a pressure support mode for delivering therapy to a user. A flow diversion device or valve switches from a first mode corresponding with the sub-therapeutic mode of the system to a second mode corresponding with the pressure support mode of the system. In the first mode, the valve opens a larger flow path between the interior of the user interface and ambient air than in the second mode.

## Claims

### Claim 1

A system for supplying respiratory gases to a user wearing a user interface, the system comprising:
a flow generator;
a controller controlling operation of the flow generator, the controller configured to:
operate the flow generator in a therapeutic mode to create a first pressure;
operate the flow generator in a subtherapeutic mode to create a second pressure, wherein the first pressure is higher than the second pressure;
determine a sleep state of the user during the supply of respiratory gases;
change the operation of the flow generator to the therapeutic mode based on the determination of the sleep state indicating that the user is asleep;
determine a change in the sleep state indicating that the user is awake based on a continuous monitoring of the user during the operation of the flow generator in the therapeutic mode;
change the operation of the flow generator to the subtherapeutic mode based on the determination of the change in the sleep state indicating the user is awake;
determine an average flow rate after changing the operation of the flow generator to the subtherapeutic mode and in response to the determination of the change in the sleep state indicating the user is awake;
compare, during the subtherapeutic mode, the average flow rate with a low flow threshold and a high flow threshold;
maintain, during the subtherapeutic mode, the average flow rate within the low flow threshold and the high flow threshold based on an adjustment of an input parameter to the flow generator after the comparison of the average flow rate;
compare, during the subtherapeutic mode, a pressure supplied to the user with a pressure threshold; and
change the operation of the flow generator from the subtherapeutic mode to the therapeutic mode based on the comparison of the average flow rate indicating that the average flow rate is less than the low flow threshold and the comparison of the pressure supplied indicating that the pressure supplied is above the pressure threshold; and
a valve, wherein the valve is configured to transition from the subtherapeutic mode to the therapeutic mode in synchrony with an inhalation of the user.

### Claim 2 (depends on 1)

The system of claim 1, wherein the valve transitions from the second mode to the first mode in synchrony with an exhalation of the user.

### Claim 3 (depends on 1)

The system of claim 1, wherein the controller is further configured to determine the user to be sleeping based upon detection of sleep disordered breathing events.

### Claim 4 (depends on 1)

The system of claim 1, wherein the controller is further configured to increase pressure in synchrony with inhalation of the user in the second mode.

### Claim 5 (depends on 1)

The system of claim 1, wherein the controller is further configured to decrease pressure in synchrony with exhalation of the user in the second mode.

### Claim 6 (depends on 1)

The system of claim 1, further comprising a port to ambient and the valve assuming a first position and a second position, when in the second position, the valve substantially closing the port, the port being positioned between the user and the flow generator.

### Claim 7 (depends on 6)

The system of claim 6, wherein the valve transitions from the first position to the second position comprises changing position of a valve member.

### Claim 8

A method for supplying respiratory gases with a flow generator to a user wearing a user interface, the method comprising:
initiating the flow generator in a subtherapeutic mode to create a second pressure lower than a first pressure of a therapeutic mode;
determining a sleep state of the user during the supply of respiratory gases;
changing the operation of the flow generator to the therapeutic mode based on the determination of the sleep state indicating that the user is asleep;
determining a change in the sleep state indicating that the user is awake based on a continuous monitoring of the user during the operation of the flow generator in the therapeutic mode;
changing the operation of the flow generator to the subtherapeutic mode based on the determination of the change in the sleep state indicating the user is awake;
determining an average flow rate after changing the operation of the flow generator to the subtherapeutic mode and in response to the determination of the change in the sleep state indicating the user is awake;
comparing, during the subtherapeutic mode, the average flow rate with a low flow threshold and a high flow threshold;
maintaining, during the subtherapeutic mode, the average flow rate within the low flow threshold and the high flow threshold based on an adjustment of an input parameter to the flow generator after the comparison of the average flow rate;
comparing, during the subtherapeutic mode, a pressure supplied to the user with a pressure threshold; and
changing the operation of the flow generator from the subtherapeutic mode to the therapeutic mode based on the comparison of the average flow rate indicating that the average flow rate is less than the low flow threshold and the comparison of the pressure supplied indicating that that pressure supplied is above the pressure threshold.