Therapeutic gas conserver and control

• US 20030140924A1
• Filed: 11/05/2002
• Published: 07/31/2003
• Est. Priority Date: 11/06/2001
• Status: Abandoned Application

• Current Assignee: Air Motion Technologies, LLC
• Original Assignee: Air Motion Technologies, LLC
• Inventors: Aylsworth, Alonzo C., Miller, Gregory R.
• Application Number:
  US10/287,899
• Publication Number:
  US 20030140924A1
• Time in Patent Office: Days
• US Class Current: 128/204.26
• CPC Class Codes: A61M 16/0051 with alarm devices
• CPC Class Codes: A61M 16/024 including calculation means, e.g. using a processor
• CPC Class Codes: A61M 16/0677 Gas-saving devices therefor
• CPC Class Codes: A61M 16/101 using an oxygen concentrator
• CPC Class Codes: A61M 16/1055 bacterial
• CPC Class Codes: A61M 16/107 in the inspiratory path
• CPC Class Codes: A61M 2016/0021 with a proportional output signal, e.g. from a thermistor
• CPC Class Codes: A61M 2016/0039 in the inspiratory circuit
• CPC Class Codes: A61M 2205/70 with testing or calibration facilities
• CPC Class Codes: A61M 2230/04 Heartbeat characteristics, e.g. ECG, blood pressure modulation
• CPC Class Codes: A61M 2230/205 partial oxygen pressure (P-O2)
• CPC Class Codes: A61M 2230/40 Respiratory characteristics
• CPC Class Codes: A61M 2230/42 Rate

Abstract

A method and device for sensing inhalations and controlling the delivery of oxygen or other therapeutic gases to a patient. A flow-through sensor is adapted to provide a method and device to monitor various parameters of a patient'"'"'s breathing and/or pulse oxygen saturation. Adjustments are made to the bolus delivery from a source of therapeutic gas to efficiently provide appropriate levels of therapeutic gas to the patient and to economically conserve therapeutic gas.

Claims

1. A therapeutic gas conserver and control device for a source of therapeutic gas comprised of:

a supply valve having a first side, a second side, and a supply side, wherein said supply side of said supply valve is connected to said source of therapeutic gas;

a flow-through sensor having a first side and a second side, wherein said second side of said sensor is connected to said first side of said supply valve;

a cal valve having a first side and a vent side, wherein said first side of said cal valve is connected to said first side of said flow-through sensor; and

the said vent side is open to atmospheric air;

a patient outlet having a first side and a second side, wherein said first side of said patient outlet is connected to said second side of said supply valve;

at least one cannula having a first side and a second side, wherein said first side of said at least one cannula is connected to said second side of said patient outlet; and

a processor in electrical communication with said supply valve, said cal valve, and said flow-through sensor, wherein said processor provides a signal to control delivery of a portion of said source of therapeutic gas to a patient through said second side of said at least one cannula,

wherein said device delivers therapeutic gas to a patient.

2. The device in claim 1 wherein said at least one cannula is a dual lumen cannula.

3. The device in claim 1 further comprising:

an extension tube connected between said second side of said patient outlet and said first side of said at least one cannula.

4. The device of claim 1 further comprising:

at least one bacterial filter connected between said second side of said patient outlet and said first side of said at least one cannula.

5. The device of claim 1 further comprising:

an alarm in electrical contact with said processor.

6. The device of claim 5, wherein said alarm provides an auditory signal through said at least one cannula.

7. The device of claim 5 wherein said alarm provides a pulse of a gas signal through said at least one cannula.

8. The device of claim 1 further comprising:

a pulse oximetry measurement device in electrical communication with said processor.

9. The device of claim 1 further comprising:

a pressure transducer connected between said second side of said supply valve and said first side of said patient outlet, wherein said pressure transducer measures a pressure of delivery of said bolus of oxygen.

10. The device of claim 9 wherein said pressure transducer is in electrical communication with said processor.

11. The device of claim 1 further comprising:

a bypass, wherein said bypass provides a connection between said source of oxygen and said patient outlet.

12. The bypass of claim 11 wherein said bypass is in electrical communication with said processor.

13. The bypass of claim 12 wherein said bypass is controlled by said processor.

14. The device of claim 12 wherein said bypass is a manually set pneumatic switch.

15. The device of claim 12 wherein said bypass is a valve.

16. The device of claim 12 wherein said bypass is an orifice.

17. The device of claim 16 wherein said orifice is a selectable orifice.

18. The device of claim 16 wherein said orifice is a proportional orifice.

19. The device of claim 1 wherein said supply valve allows a desired quantity of said source of oxygen to continuously flow through said supply valve.

20. The device of claim-1 further comprising a supply compressor connected between said source of oxygen and said supply side of said supply valve, wherein said supply compressor raises the pressure of a supply of oxygen through said supply valve.

21. The supply compressor of claim 20 wherein said supply compressor is pneumatically powered.

22. The supply compressor of claim 20 wherein said supply compressor is electrically powered.

23. The supply compressor of claim 20 wherein said supply compressor is in electrical communication with said processor.

24. The supply compressor of claim 20 wherein said supply compressor is controlled by said processor.

25. The device of claim 1 further comprising a bypass compressor connected between said source of therapeutic gas and said first side of said patient outlet, wherein said bypass compressor raises the pressure of a supply of oxygen through said patient outlet.

26. The bypass compressor of claim 25 wherein said bypass compressor is pneumatically powered.

27. The bypass compressor of claim 25 wherein said bypass compressor is electrically powered.

28. The bypass compressor of claim 25 wherein said bypass compressor is in electrical communication with said processor.

29. The bypass compressor of claim 28 wherein said bypass compressor is controlled by said processor.

30. The device of claim 1 wherein said source of therapeutic gas is oxygen.

31. The device of claim 30 wherein said source of oxygen is an oxygen supply line from a centralized reservoir of oxygen.

32. The device of claim 30 wherein said source of oxygen is a tank of compressed oxygen.

33. The device of claim 30 wherein said source of oxygen is an oxygen generator.

34. The device of claim 33 wherein said oxygen generator is a ceramic oxygen generator.

35. The device of claim 1 whereas said at least one cannula is a pneumatic circuit terminated at a point of a patient inspiratory device.

36. The device in claim 1 further comprising:

a vent tube having a first end, a second end, and a tube volume, wherein said first end of said vent tube is open to atmospheric air and said second end of said vent tube is connected to said vent side of said cal valve;

wherein a volume of gas displaced during respiration of said patient is less than said vent tube volume.

37. The device in claim 1 further comprising:

a vent tube having a first end, a second end, and a tube volume, wherein said first end of said vent tube is connected to said first end of said cal valve and said second end of vent tube is connected to said first end of the flow through sensor;

wherein a volume of gas displaced during respiration of said patient is less than said vent tube volume.

38. The device in claim 1 whereas the processor is battery powered.

39. The device of claim 32 further comprising:

a backup supply of oxygen, wherein said backup supply of oxygen is connected to said supply side of said supply valve.

40. The device of claim 1 further comprising:

a backup supply of oxygen, wherein said backup supply of oxygen is connected to said first side of said patient outlet.

92. The device of claim 1 wherein said supply valve is remotely located near said patient and, said supply valve is in electrical communication with said processor, and said communication method between said supply valve and said processor is through electrical wires within said cannula.

93. The device of claim 1 wherein said flow-through sensor is remotely located near said patient.

94. The device of claim 93 wherein said electrical wires conduct modulated signals to said flow-through sensor and said supply valve along said electrical wires.

95. The device of claim 93 wherein the electrical wires are the power supply wires.

41. A therapeutic gas conserver and control device for a source of therapeutic gas comprised of:

A therapeutic gas supply system;

a flow-through sensor connected to said therapeutic gas supply system;

a vent system connected to said flow-through sensor; and

a processor in electrical communication with said therapeutic gas supply system, and said flow-through sensor, and said vent system.

42. The device of claim 41 wherein said vent system is comprised of:

a cal valve; and

a vent tube connected to said cal valve.

43. The device of claim 41 wherein said therapeutic gas supply system is comprised of:

a supply valve; and

a patient outlet connected to said supply valve.

44. The device of claim 43 wherein said therapeutic gas supply system is further comprised of:

a bypass connected between said source of therapeutic gas and said patient outlet.

45. The device of claim 44 wherein said bypass is in electrical communication with said processor.

46. The device of claim 44 wherein said therapeutic gas supply system is further comprised of:

at least one cannula connected to said patient outlet.

47. The device of claim 46 wherein said therapeutic gas supply system is further comprised of:

an extension tube connected between said patient outlet and said at least one cannula.

48. The device of claim 46 wherein said therapeutic gas supply system is further comprised of:

a pressure transducer connected between said supply valve and said at least one cannula, wherein said pressure transducer is in electrical communication with said processor.

49. The device of claim 46 wherein said therapeutic gas supply system is further comprised of:

a bacterial filter connected between said supply valve and said at least one cannula.

50. The device of claim 41 further comprised of:

an alarm in electrical contact with said processor.

51. The device of claim 41 further comprised of:

a pulse oximetry measurement device in electrical contact with said processor.

52. The device of claim 41 further comprised of:

a supply compressor connected between said source of therapeutic gas and said therapeutic gas supply system.

53. The device of claim 52 wherein said supply compressor is in electrical communication with said processor.

54. The device of claim 53 wherein said supply compressor is controlled by said processor.

55. The device of claim 41 further comprising:

a backup supply of therapeutic gas connected to said therapeutic gas supply system.

73. The device of claim 41 wherein said therapeutic gas source is atmospheric air under pressure.

74. The device of claim 41 wherein said therapeutic gas source is oxygen under pressure.

56. A method of conserving and controlling the delivery of a source of therapeutic gas to a patient, the steps comprised of:

providing a flow-through sensor in electrical communication with a processor;

providing a therapeutic gas supply system in electrical communication with said processor;

measuring at least one parameter of respiration of said patient;

providing an algorithm for said processor to evaluate said measured at least one parameter of respiration;

adjusting delivery of at least one bolus of therapeutic gas from said source of therapeutic gas to said patient in response to said evaluation of said at least one measured parameter of respiration.

57. The method of claim 56 wherein said at least one parameter of respiration is selected from the group consisting of respiratory effort, respiratory rate, activity, blood oxygen level, minute volume, heart rate, apnea, and hypopnea.

58. The method of claim 56 further comprising:

providing an algorithm for said processor to calibrate and configure use of said source of therapeutic gas, said flow-through sensor, and said therapeutic gas supply system.

59. The method of claim 58 whereas said calibration is in response to at least one environmental condition.

60. The method of claim 56 further comprising:

providing an algorithm for said processor to periodically calibrate use of said source of therapeutic gas, said flow-through sensor, and said therapeutic gas supply system.

61. The method of claim 56 further comprising:

automatically activating said measurement of at least one parameter of respiration from a signal by said flow-through sensor sent to said processor.

62. The method of claim 56 further comprising:

providing an algorithm for said processor to estimate at least one parameter of delivery of subsequent said at least one bolus of therapeutic gas from said source of therapeutic gas to said patient; and

delivering said at least one bolus of therapeutic gas according to said at least one estimated parameter of delivery.

63. The method of claim 62 wherein said parameter of delivery is selected from the group consisting of time, frequency, duration, volume, and pressure.

64. The method of claim 56 further comprising:

providing an algorithm for said processor to determine the occurrence of apnea events by evaluation of said measured at least one parameter of respiration.

65. The method of claim 64 further comprising:

communicating information of said apnea events determined by said processor to a receiving device.

66. The method of claim 64 further comprising:

communicating an alarm signal of said apnea events determined by said processor.

67. The method of claim 64 further comprising:

storing data of said apnea events determined by said processor.

68. The method of claim 56 further comprising:

providing an algorithm for said processor to evaluate and reject a rhythmic artifact.

69. The method of claim 56 further comprising:

providing an algorithm for said processor to provide a lockout time, whereby signals from said flow-through sensor are disregarded for a duration of time.

70. The method of claim 56 further comprising:

providing an algorithm for said processor to provide reset hysteresis.

71. The method of claim 70 whereas said lockout time is a percentage of the time between at least two previous patient inspirations.

72. The method in claim 56 wherein said therapeutic gas is pressurized atmospheric air.

75. A method of conserving and controlling the delivery of a source of therapeutic gas to a patient, the steps comprised of:

providing a diaphragm-based sensor in electrical communication with a processor;

providing a therapeutic gas supply system in electrical communication with said processor;

measuring at least one parameter of respiration of said patient;

providing an algorithm for said processor to evaluate said measured at least one parameter of respiration;

adjusting delivery of at least one bolus of therapeutic gas from said source of therapeutic gas to said patient in response to said evaluation of said at least one measured parameter of respiration.

76. The method of claim 75 wherein said at least one parameter of respiration is selected from the group consisting of respiratory effort, respiratory rate, activity, blood oxygen level, minute volume, heart rate, apnea, and hypopnea.

77. The method of claim 75 further comprising:

providing an algorithm for said processor to calibrate and configure use of said source of therapeutic gas, said diaphragm-based sensor, and said therapeutic gas supply system.

78. The method of claim 77 whereas said calibration is in response to at least one environmental condition.

79. The method of claim 75 further comprising:

providing an algorithm for said processor to periodically calibrate use of said source of therapeutic gas, said diaphragm-based sensor, and said therapeutic gas supply system.

80. The method of claim 75 further comprising:

automatically activating said measurement of at least one parameter of respiration from a signal by said diaphragm-based sensor sent to said processor.

81. The method of claim 75 further comprising:

providing an algorithm for said processor to estimate at least one parameter of delivery of subsequent said at least one bolus of therapeutic gas from said source of therapeutic gas to said patient; and

delivering said at least one bolus of therapeutic gas according to said at least one estimated parameter of delivery.

82. The method of claim 81 wherein said parameter of delivery is selected from the group consisting of time, frequency, duration, volume, and pressure.

83. The method of claim 75 further comprising:

providing an algorithm for said processor to determine the occurrence of apnea events by evaluation of said measured at least one parameter of respiration.

84. The method of claim 83 further comprising:

communicating information of said apnea events determined by said processor to a receiving device.

85. The method of claim 83 further comprising:

communicating an alarm signal of said apnea events determined by said processor.

86. The method of claim 83 further comprising:

storing data of said apnea events determined by said processor.

87. The method of claim 75 further comprising:

providing an algorithm for said processor to evaluate and reject a rhythmic artifact.

88. The method of claim 75 further comprising:

providing an algorithm for said processor to provide a lockout time, whereby signals from said flow-through sensor are disregarded for a duration of time.

89. The method of claim 75 further comprising:

providing an algorithm for said processor to provide reset hysteresis.

90. The method of claim 88 whereas said lockout time is a percentage of the time between at least two previous patient inspirations.

91. The method in claim 75 wherein said therapeutic gas is pressurized atmospheric air.