Respiratory aid apparatus and method

• US 7,562,659 B2
• Filed: 07/22/2003
• Issued: 07/21/2009
• Est. Priority Date: 07/22/2002
• Status: Expired due to Fees

• Current Assignee: Intellibreathe, Ltd.
• Original Assignee: Hasdi Matarasso
• Inventors: Matarasso, Hasdi
• Primary Examiner(s): Yu; Justine R
• Assistant Examiner(s): OSTRUP, CLINTON T
• Application Number:
  US10/522,073
• Publication Number:
  US 20060011198A1
• Time in Patent Office: 2,191 Days
• Field of Search: 128/204.25, 128/200.24, 128/202.24, 128/204.18, 128/204.21, 128/204.22, 128/204.26, 128/205.11, 128/205.23, 128/205.24, 128/205.25, 128/206.22, 128/207.18
• US Class Current: 128/207.18
• CPC Class Codes: A61M 16/0012 by Venturi means
• CPC Class Codes: A61M 16/0063 Compressors
• CPC Class Codes: A61M 16/0066 Blowers or centrifugal pumps
• CPC Class Codes: A61M 16/0069 the speed thereof being controlled by respiratory parameters, e.g. by inhalation
• CPC Class Codes: A61M 16/0493 with means for protecting the tube from damage caused by the patient's teeth, e.g. bite block
• CPC Class Codes: A61M 16/06 Respiratory or anaesthetic masks
• CPC Class Codes: A61M 16/0666 Nasal cannulas or tubing devices for improving normal breathing through the nose A61F5/08; nose filters A62B23/06; outside holding devices A61M25/02
• CPC Class Codes: A61M 16/127 by Venturi effect, i.e. entrainment mixers
• CPC Class Codes: A61M 16/16 Devices to humidify the respiration air A61M16/1045 takes precedence
• CPC Class Codes: A61M 16/161 with means for measuring the humidity
• CPC Class Codes: A61M 2016/0021 with a proportional output signal, e.g. from a thermistor
• CPC Class Codes: A61M 2205/3368 Temperature
• CPC Class Codes: A61M 2205/3375 Acoustical, e.g. ultrasonic, measuring means
• CPC Class Codes: A61M 2205/8225 using incorporated gas cartridges for the driving gas

Abstract

A system and method are disclosed for the provision of assisted breathing by the delivery of a controlled pressurized airflow to the pulmonary airway of a user with breathing disorders. The system comprises a source of compressed respiratory gas (112), a user interface unit (115) including at least one Venturi device (120) and a thin flexible tubing (116) connecting between the source of high pressure gas (112) and the Venturi device. The system and method provide a regulated and controlled flow of air to the user (105) in accordance with the user needs. The invention further discloses a novel small light-weight user interface for replacing prior art breathing masks.

Claims

1. A portable respiratory aid system for administrating a regulated flow of air to a person suffering from sleep apnea, the respiratory aid system comprising:

a source of high pressure air;

an air delivery nasal interface comprising two air delivery units configured for delivering a flow of air each to a respective nostril of said person, the two air delivery units being pivotally mounted on opposite ends of a flat elongated flexible member configured to be placed above the upper lip of said person, wherein each of said two air delivery units comprises a Venturi device, said Venturi device comprising a hollow member defining a central space and an inlet which opens into said central space, a first open end opens to surrounding ambient air and a second open end being provided with a nasal adaptor attachable to a nostril of said person, wherein said first inlet is configured for receiving a flow of high pressure air via a thin flexible tubing and for directing said flow of high pressure air toward said second open end; and

a thin flexible tubing bifurcating into two branches for delivering a flow of high pressure air from said source of high pressure air to said inlet of each Venturi device, said tubing being configured for serving as strapping means for strapping said air delivery nasal interface to said person'"'"'s head;

at least one sensor for monitoring breathing of said person;

and

a control unit operably connected to said at least one sensor for regulating said flow of high pressure air in accordance with said monitored breathing, the control unit comprising a microprocessor and a memory device configured for monitoring a breathing pattern over time, thereby enabling a real-time regulation of said flow of air in accordance with respiratory cycles of said person and a long term regulation in accordance with said monitored breathing pattern.

2. The respiratory aid system of claim 1 wherein the thin tubing diameter is in the range of 2 to 5 mm and wherein said source of high pressure air has an output pressure in the range of 2 to 6 Atmospheres.

3. The respiratory aid system of claim 1 wherein said source of high pressure air is a portable container of compressed air.

4. The respiratory aid system of claim 1 wherein said source of high pressure air is an oil-less air compressor.

5. The respiratory aid system of claim 4 wherein said control unit is operably connected to said oil-less compressor.

6. The respiratory aid system of claim 1 wherein said at least one sensor is a sound transducer or a temperature detector.

7. The respiratory aid system of claim 1 wherein said at least one sensor is a pressure detector.

8. The respiratory aid system of claim 1 further comprising a controllable valve operably connected to said control unit, said controllable valve is interposed between said source of high pressure air and said first inlet of the at least one Venturi device.

9. The respiratory aid system of claim 8 wherein said controllable valve is an on/off valve.

10. The respiratory aid system of claim 8 wherein said controllable valve is a flow regulation valve.

11. The respiratory aid system of claim 1 further comprising a chest-mounted sensor adapted for detecting expansion and contraction of the chest of the person.

12. The respiratory aid system of claim 1 wherein at least one of said Venturi device further comprises a second inlet which opens into said central space and wherein said second inlet is configured for receiving a flow of high pressure air and for directing said flow of high pressure air toward said first open end.

13. The respiratory air system of claim 1 wherein said long term regulation in accordance with said monitored breathing pattern comprises turning on said flow of high pressure air upon detection of a breathing disorder and turning it off upon detection of a regular non-obstructive breathing.

14. An air delivery nasal interface comprising:

two air delivery units configured for delivering a flow of air to one of a pair of nostrils of a person, said two air delivery units being pivotally mounted on opposite ends of a flat elongated flexible member configured to be placed above the upper lip of said person, wherein each of said two air delivery units comprises a Venturi device, wherein each of said Venturi devices comprises a hollow chamber defining a central space, and an inlet which opens into said central space, said hollow member having a first open end which opens to surrounding ambient air and a second open end provided with a nasal adaptor, wherein the inlet of each of said Venturi devices is configured to receive a flow of high pressure air via a thin tubing and to direct said flow of high pressure air toward said second open end, wherein said flow of high pressure air upon entering said central space acts as a driving force for drawing ambient air through said first end toward said second open end;

a thin flexible tubing bifurcating into two branches for connecting a source of high pressure air to each of said inlets of said two air delivery units, said tubing being configured for serving as strapping means for strapping said air delivery nasal interface to a person'"'"'s head; and

at least one sensor for monitoring breathing of a person using the air delivery nasal interface.

15. The air delivery nasal interface of claim 14 wherein said at least one sensor is a sound transducer or a temperature detector.

16. The air delivery nasal interface of claim 14 wherein said at least one sensor is a pressure detector.

17. The air delivery nasal interface of claim 14 further comprising a controllable valve interposed upstream of the two first inlets of said two air delivering units.

18. The air delivery nasal interface of claim 14 wherein the at least one Venturi devices further comprises a second inlet which opens into said central space and wherein said second inlet is configured for receiving a flow of high pressure air and to direct said flow of high pressure air toward said first open end.

19. The air delivery nasal interface of claim 18 further comprising a controllable valve operably interposed between said first and second inlets, the controllable valve is configured for allowing direction of flow to either the first inlet or to the second inlet.

20. A method for administrating a controlled flow of air to a person suffering from sleep apnea, in accordance with the real-time needs of said person, the method comprising:

connecting a portable source of high pressure air by means of a thin tubing to an air delivery nasal interface wherein the air delivery nasal interface comprises two air delivery units configured for delivering a flow of air each to a respective nostril of said person, the two air delivery units being pivotally mounted on opposite ends of a flat elongated flexible member configured to be placed above the upper lip of said person, wherein each of said two air delivery units comprises a Venturi device, both Venturi devices, comprising a hollow member defining a central space, an inlet that opens into said central space, each hollow member having a first open end that opens into surrounding ambient air and a second open end provided with a nasal adaptor attachable to a person'"'"'s nostril, each of said Venturi devices being configured to receive a flow of high pressure air through said inlet and to direct said flow of high pressure air toward said second end, thereby drawing ambient air from said first open end toward said second open end and reducing said high pressure to a pressure of lower value;

monitoring the breathing of said person by means of a sensor; and

delivering a flow of high pressure air from said source of high pressure air via said thin tubing to said air delivery nasal interface via the inlets of said Venturi devices; and

automatically regulating said flow of high pressure air in accordance with the monitored breathing so as to administer a flow of a desired pressure to said person when an apneic breathing pattern is detected and turning off the flow of high pressure air upon detection of a regular non-obstructed breathing.

21. The method of claim 20 wherein said source of high pressure air is a container of high pressure air.

22. The method of claim 20 wherein said source of high pressure air is an oil-less air compressor.

23. The method of claim 20, wherein said regulating the flow of air in accordance with the monitored breathing comprises the steps of:

automatically turning off the flow of high pressure during exhalation phase; and

automatically turning on the flow of high pressure air during inhalation phase.