IP Library › Granted Patent US 11,833,301
Granted Patent B2
US 11,833,301 · App. 15/250,834 · Granted Dec 5, 2023

High flow therapy device utilizing a non-sealing respiratory interface and related methods

Inventors: Robert M Landis (Mountainside, NJ); Charles A Lewis (Carrabelle, FL); Louis Javier Collazo (Pompano Beach, FL)
A61M16/0069A61J11/0005A61M16/0051A61M16/0057A61M16/0493A61M16/0666A61M16/0677A61M16/085A61M16/0858A61M16/107A61M16/109A61M16/1075A61M16/1095A61M16/12A61M16/125A61M16/142A61M16/16A61M16/20A61M16/203A61M16/0066A61M16/18A61M2016/0024A61M2016/0027A61M2016/103A61M2016/1025A61M2202/0208A61M2205/18A61M2205/3334A61M2205/3368A61M2205/3653A61M2205/50A61M2230/005A61M2230/42A61M2230/432A61M2230/435A61M2230/50
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Quick Facts
Patent No.
US 11,833,301
App. No.
15/250,834
Filed
Aug 29, 2016
Granted
Dec 5, 2023
Kind
B2
Art Unit
3785
USPC
424/725
Abstract

A high flow therapy system for delivering heated and humidified respiratory gas to an airway of a patient includes a respiratory gas flow pathway for delivering the respiratory gas to the airway of the patient by way of a non-sealing respiratory interface; wherein flow rate of the respiratory gas is controlled by a microprocessor, a mixing area for mixing a first gas and a second gas in the respiratory gas flow pathway, a humidification area downstream of the mixing area and configured for humidifying respiratory gas in the respiratory gas flow pathway, and a heated delivery conduit for minimizing condensation of humidified respiratory gas.

Claims (60)

1. A high flow therapy system for delivering heated and humidified respiratory gas to an airway of a patient, the system comprising:

a microprocessor;

a respiratory gas flow pathway for delivering the respiratory gas to the airway of the patient by way of a non-sealing respiratory interface, wherein flow rate of the respiratory gas is controlled by the microprocessor;

a mixing area for mixing oxygen and air in the respiratory gas flow pathway;

a humidification area downstream of the mixing area and configured for humidifying respiratory gas in the respiratory gas flow pathway; and

a heated delivery conduit for minimizing condensation of humidified respiratory gas;

wherein the non-sealing respiratory interface is configured to form a passageway for exhaled gas of the patient to pass to ambient atmosphere without passing through a remainder of the system,

wherein the non-sealing respiratory interface includes:

a tubular base portion;

at least one nozzle defining at least one inlet; and

at least one outlet member defining an outlet, the at least one outlet member being substantially parallel to the at least one nozzle, the at least one outlet member and the at least one nozzle positioned on opposite sides of the base portion,

wherein the at least one inlet is in gaseous communication with the outlet.

2. The high flow therapy system of claim 1 , wherein at least one of respiration rate, tidal volume and minute volume are calculated by the microprocessor.

3. The high flow therapy system of claim 1 , wherein the microprocessor is configured to control at least one of temperature of the gas, humidity of the gas, mixture of the gas, the flow rate of the gas, and volume of the gas delivered to the patient.

4. The high flow therapy system of claim 1 , wherein the microprocessor is configured to adjust flow rates based on at least one of a pre-programmed algorithm and a setting inputted by an operator.

5. The high flow therapy system of claim 1 , wherein the system is configured to signal an alarm when conditions deviate from pre-determined criteria.

6. The high flow therapy system of claim 1 , wherein the system is configured to control the flow rate of the respiratory gas delivered to the patient based on a respiratory phase of the patient during use.

7. The high flow therapy system of claim 1 , wherein the system is configured to deliver the respiratory gas to the patient at different airway pressures based on a respiratory phase of the patient during use.

8. The high flow therapy system of claim 1 , further comprising a gas analyzer.

9. The high flow therapy system of claim 1 , further comprising a display.

10. The high flow therapy system of claim 1 , further comprising a proportional valve.

11. The high flow therapy system of claim 1 , wherein the non-sealing respiratory interface includes a nasal cannula.

12. The high flow therapy system of claim 1 , further comprising a gas inlet configured to connect to an external source of gas.

13. The high flow therapy system of claim 1 , wherein the non-sealing respiratory interface includes at least one conduit configured to extend from the inlet through the at least one nozzle, through the base portion, and to the outlet.

14. The high flow therapy system of claim 1 , wherein the at least one inlet is connected to a conduit that is configured to route gas to a sensor.

15. The high flow therapy system of claim 1 , wherein the at least one inlet includes:

a first inlet that is connected to a first conduit configured to route gas to a first sensor; and

a second inlet that is connected to a second conduit configured to route gas to a second sensor, wherein the second conduit is physically separate from the first conduit.

16. The high flow therapy system of claim 1 , wherein the outlet is located at an end of the at least one outlet member.

17. The high flow therapy system of claim 1 , wherein the at least one outlet member is configured to connect to a sensor via accessory tubing.

18. The high flow therapy system of claim 1 , further comprising a blower.

19. The high flow therapy system of claim 18 , wherein the blower is configured for providing a patient with gas flow rates of up to 60 liters per minute.

20. The high flow therapy system of claim 1 , wherein the non-sealing respiratory interface includes a sensor mounted thereon configured to measure a pressure in the airway of the patient, and wherein the sensor is configured to monitor the airway of the patient.

21. The high flow therapy system of claim 20 , wherein the sensor communicates information on the monitored airway of the patient to the microprocessor.

22. The high flow therapy system of claim 20 , wherein the sensor is configured to measure at least one of inspiration pressure and expiration pressure of the patient.

23. The high flow therapy system of claim 20 , wherein the sensor is at least partially enclosed within the respiratory gas flow pathway.

24. A high flow therapy system for delivering heated and humidified respiratory gas to an airway of a patient, the system comprising:

a microprocessor;

a respiratory gas flow pathway for delivering the respiratory gas to the airway of the patient by way of a non-sealing respiratory interface, wherein flow rate of the respiratory gas is controlled by the microprocessor;

a blower controlled by the microprocessor;

a mixing area for mixing a first gas and a second gas in the respiratory gas flow pathway;

a humidification area downstream of the mixing area and for humidifying respiratory gas in the respiratory gas flow pathway; and

a heated delivery conduit for minimizing condensation of humidified respiratory gas; and wherein the non-sealing respiratory interface is configured to form a passageway for exhaled gas of the patient to pass to ambient atmosphere without passing through a remainder of the system.

wherein the non-sealing respiratory interface includes:

a tubular base portion;

at least one nozzle defining at least one inlet; and

at least one outlet member defining an outlet, the at least one outlet member being substantially parallel to the at least one nozzle, the at least one outlet member and the at least one nozzle positioned on opposite sides of the base portion,

wherein the at least one inlet is in gaseous communication with the outlet.

25. A high flow therapy system for delivering heated and humidified respiratory gas to an airway of a patient, the system comprising:

a microprocessor;

a respiratory gas flow pathway for delivering the respiratory gas to the airway of the patient by way of a non-sealing respiratory interface, wherein flow rate of the respiratory gas is controlled by the microprocessor located within a housing;

a mixing area located within the housing for mixing a first gas and a second gas in the respiratory gas flow pathway;

a humidification area downstream of the mixing area and located outside of the housing for humidifying respiratory gas in the respiratory gas flow pathway;

a heating element in thermal communication with the humidification area; and

a heated delivery conduit for minimizing condensation of humidified respiratory gas; wherein the non-sealing respiratory interface is configured to form a passageway for exhaled gas of the patient to pass to ambient atmosphere without passing through a remainder of the system.

wherein the non-sealing respiratory interface includes:

a tubular base portion;

at least one nozzle defining at least one inlet; and

at least one outlet member defining an outlet, the at least one outlet member being substantially parallel to the at least one nozzle, the at least one outlet member and the at least one nozzle positioned on opposite sides of the base portion,

wherein the at least one inlet is in gaseous communication with the outlet.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 9, 2020
From: MERGENET MEDICAL, INC.
To: RESMED PTY LTD
Reel/Frame 053719/0900 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 9, 2020
From: LANDIS, ROBERT M.; LEWIS, CHARLES A.; COLLAZO, LOUIS JAVIER
To: MERGENET MEDICAL, INC.
Reel/Frame 054172/0486 →
Continuity (7)
Continuation 13717442 · Dec 17, 2012
Continuation 11638981 · Dec 14, 2006
Continuation In Part 11520490 · Sep 12, 2006
Provisional Application 60716776 · Sep 12, 2005
Provisional Application 60792711 · Apr 18, 2006
Provisional Application 60750063 · Dec 14, 2005
Related Publication 20160367776A1 · Dec 22, 2016