WO2011143198A2 - Patient circuit integrity alarm using exhaled c02 - Google Patents

Patient circuit integrity alarm using exhaled c02 Download PDF

Info

Publication number
WO2011143198A2
WO2011143198A2 PCT/US2011/035899 US2011035899W WO2011143198A2 WO 2011143198 A2 WO2011143198 A2 WO 2011143198A2 US 2011035899 W US2011035899 W US 2011035899W WO 2011143198 A2 WO2011143198 A2 WO 2011143198A2
Authority
WO
WIPO (PCT)
Prior art keywords
carbon dioxide
patient
amount
dioxide sensor
gas
Prior art date
Application number
PCT/US2011/035899
Other languages
French (fr)
Other versions
WO2011143198A3 (en
Inventor
Paul David Dixon
Terry Lee Blansfield
Original Assignee
Carefusion 207, Inc.
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Carefusion 207, Inc. filed Critical Carefusion 207, Inc.
Priority to MX2012012791A priority Critical patent/MX2012012791A/en
Priority to EP11781131.5A priority patent/EP2569036B1/en
Priority to CN201180023261.XA priority patent/CN103002939B/en
Priority to BR112012028156-9A priority patent/BR112012028156B1/en
Publication of WO2011143198A2 publication Critical patent/WO2011143198A2/en
Publication of WO2011143198A3 publication Critical patent/WO2011143198A3/en

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61MDEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M16/00Devices for influencing the respiratory system of patients by gas treatment, e.g. mouth-to-mouth respiration; Tracheal tubes
    • A61M16/0051Devices for influencing the respiratory system of patients by gas treatment, e.g. mouth-to-mouth respiration; Tracheal tubes with alarm devices
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61MDEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M16/00Devices for influencing the respiratory system of patients by gas treatment, e.g. mouth-to-mouth respiration; Tracheal tubes
    • A61M16/021Devices for influencing the respiratory system of patients by gas treatment, e.g. mouth-to-mouth respiration; Tracheal tubes operated by electrical means
    • A61M16/022Control means therefor
    • A61M16/024Control means therefor including calculation means, e.g. using a processor
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61MDEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M16/00Devices for influencing the respiratory system of patients by gas treatment, e.g. mouth-to-mouth respiration; Tracheal tubes
    • A61M16/10Preparation of respiratory gases or vapours
    • A61M16/12Preparation of respiratory gases or vapours by mixing different gases
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61MDEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M16/00Devices for influencing the respiratory system of patients by gas treatment, e.g. mouth-to-mouth respiration; Tracheal tubes
    • A61M16/20Valves specially adapted to medical respiratory devices
    • A61M16/208Non-controlled one-way valves, e.g. exhalation, check, pop-off non-rebreathing valves
    • A61M16/209Relief valves
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61MDEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M16/00Devices for influencing the respiratory system of patients by gas treatment, e.g. mouth-to-mouth respiration; Tracheal tubes
    • A61M16/06Respiratory or anaesthetic masks
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61MDEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M16/00Devices for influencing the respiratory system of patients by gas treatment, e.g. mouth-to-mouth respiration; Tracheal tubes
    • A61M16/08Bellows; Connecting tubes ; Water traps; Patient circuits
    • A61M16/0816Joints or connectors
    • A61M16/0833T- or Y-type connectors, e.g. Y-piece
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61MDEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M16/00Devices for influencing the respiratory system of patients by gas treatment, e.g. mouth-to-mouth respiration; Tracheal tubes
    • A61M16/10Preparation of respiratory gases or vapours
    • A61M16/14Preparation of respiratory gases or vapours by mixing different fluids, one of them being in a liquid phase
    • A61M16/16Devices to humidify the respiration air
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61MDEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M16/00Devices for influencing the respiratory system of patients by gas treatment, e.g. mouth-to-mouth respiration; Tracheal tubes
    • A61M16/20Valves specially adapted to medical respiratory devices
    • A61M16/201Controlled valves
    • A61M16/202Controlled valves electrically actuated
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61MDEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M16/00Devices for influencing the respiratory system of patients by gas treatment, e.g. mouth-to-mouth respiration; Tracheal tubes
    • A61M16/0003Accessories therefor, e.g. sensors, vibrators, negative pressure
    • A61M2016/0015Accessories therefor, e.g. sensors, vibrators, negative pressure inhalation detectors
    • A61M2016/0018Accessories therefor, e.g. sensors, vibrators, negative pressure inhalation detectors electrical
    • A61M2016/0021Accessories therefor, e.g. sensors, vibrators, negative pressure inhalation detectors electrical with a proportional output signal, e.g. from a thermistor
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61MDEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M16/00Devices for influencing the respiratory system of patients by gas treatment, e.g. mouth-to-mouth respiration; Tracheal tubes
    • A61M16/0003Accessories therefor, e.g. sensors, vibrators, negative pressure
    • A61M2016/0027Accessories therefor, e.g. sensors, vibrators, negative pressure pressure meter
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61MDEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M16/00Devices for influencing the respiratory system of patients by gas treatment, e.g. mouth-to-mouth respiration; Tracheal tubes
    • A61M16/0003Accessories therefor, e.g. sensors, vibrators, negative pressure
    • A61M2016/003Accessories therefor, e.g. sensors, vibrators, negative pressure with a flowmeter
    • A61M2016/0033Accessories therefor, e.g. sensors, vibrators, negative pressure with a flowmeter electrical
    • A61M2016/0036Accessories therefor, e.g. sensors, vibrators, negative pressure with a flowmeter electrical in the breathing tube and used in both inspiratory and expiratory phase
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61MDEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M16/00Devices for influencing the respiratory system of patients by gas treatment, e.g. mouth-to-mouth respiration; Tracheal tubes
    • A61M16/0003Accessories therefor, e.g. sensors, vibrators, negative pressure
    • A61M2016/003Accessories therefor, e.g. sensors, vibrators, negative pressure with a flowmeter
    • A61M2016/0033Accessories therefor, e.g. sensors, vibrators, negative pressure with a flowmeter electrical
    • A61M2016/0039Accessories therefor, e.g. sensors, vibrators, negative pressure with a flowmeter electrical in the inspiratory circuit
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61MDEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M16/00Devices for influencing the respiratory system of patients by gas treatment, e.g. mouth-to-mouth respiration; Tracheal tubes
    • A61M16/0003Accessories therefor, e.g. sensors, vibrators, negative pressure
    • A61M2016/003Accessories therefor, e.g. sensors, vibrators, negative pressure with a flowmeter
    • A61M2016/0033Accessories therefor, e.g. sensors, vibrators, negative pressure with a flowmeter electrical
    • A61M2016/0042Accessories therefor, e.g. sensors, vibrators, negative pressure with a flowmeter electrical in the expiratory circuit
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61MDEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M16/00Devices for influencing the respiratory system of patients by gas treatment, e.g. mouth-to-mouth respiration; Tracheal tubes
    • A61M16/10Preparation of respiratory gases or vapours
    • A61M16/1005Preparation of respiratory gases or vapours with O2 features or with parameter measurement
    • A61M2016/102Measuring a parameter of the content of the delivered gas
    • A61M2016/103Measuring a parameter of the content of the delivered gas the CO2 concentration
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61MDEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M2205/00General characteristics of the apparatus
    • A61M2205/13General characteristics of the apparatus with means for the detection of operative contact with patient, e.g. lip sensor
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61MDEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M2205/00General characteristics of the apparatus
    • A61M2205/18General characteristics of the apparatus with alarm
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61MDEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M2205/00General characteristics of the apparatus
    • A61M2205/58Means for facilitating use, e.g. by people with impaired vision
    • A61M2205/583Means for facilitating use, e.g. by people with impaired vision by visual feedback
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61MDEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M2230/00Measuring parameters of the user
    • A61M2230/40Respiratory characteristics
    • A61M2230/43Composition of exhalation
    • A61M2230/432Composition of exhalation partial CO2 pressure (P-CO2)

Definitions

  • Lung ventilators provide therapeutic gas (e.g., oxygen) and pressure volume support to a patient's lungs in order to facilitate gas exchange with a patient, either by supporting spontaneous breathing or by providing mandatory ventilation in the absence of spontaneous breathing.
  • the gas is provided to a patient through an inspiratory conduit and the ventilator is fluidly coupled to the lung using a patient interface such as an endotracheal tube, a nasal cannula or a mask.
  • a patient interface such as an endotracheal tube, a nasal cannula or a mask.
  • a respiratory therapy system includes an inspiratory conduit and an expiratory port.
  • a patient interface is fluidly coupled to the inspiratory conduit and the expiratory port.
  • the patient interface is further configured to be coupled to a patient.
  • a carbon dioxide sensor is fluidly coupled to the expiratory port and provides an indication of whether the patient interface is fluidly coupled to the patient.
  • a respiratory therapy system includes a ventilator configured to provide inhaled gas to a patient and receive exhaled gas from the patient.
  • the respiratory therapy system also includes a carbon dioxide sensor determining an amount of carbon dioxide in the exhaled gas and comparing the amount to a threshold.
  • a method of providing respiratory therapy to a patient includes providing a patient interface configured to be fluidly coupled to the patient. Gas is provided to the patient interface through an inspiratory conduit and exhaled gas is received from the patient. An amount of carbon dioxide is measured in the exhaled gas and an indication of fluid coupling between the patient interface and the patient is provided as a function of the amount of carbon dioxide.
  • FIG. 1 is a schematic diagram of a first embodiment of a respiratory therapy system.
  • FIG. 2 is a schematic diagram of a second embodiment of a respiratory therapy system.
  • FIG 3. is a schematic diagram of a third embodiment of a respiratory therapy system.
  • FIG. 4 is a schematic diagram of a fourth embodiment of a respiratory therapy system.
  • FIG. 5 is a schematic diagram of a mask having a carbon dioxide sensor coupled thereto.
  • FIG. 6 is a graph of carbon dioxide measured from exhaled gas of a respiratory therapy system as a function of time.
  • FIG. 1 is a schematic view of a respiratory therapy system 10 including a ventilator
  • ventilator 12 supplies gases to humidifier 14 through an initial conduit 20.
  • Humidifier 14 heats water within a humidification chamber to form water vapor, which mixes with gas provided by the ventilator 12, which is then output to patient circuit 16.
  • Patient circuit 16 includes an inspiratory conduit (or limb) 22, a y-connector 24 and an expiratory conduit (or limb) 26.
  • the y-connector 24 and/or expiratory conduit 26 can be eliminated.
  • humidifier 14 can be eliminated and thus the patient is provided with dry breathing gas.
  • Y-connector 24 includes an inspiratory port 28, a patient port 30 and an expiratory port 32.
  • Inspiratory conduit 22 is fluidly coupled to the inspiratory port 28, so that gases from ventilator 12 are transferred from the inspiratory port 28 to the patient port 30.
  • Patient port 30, is fluidly coupled to a patient interface 34 that is configured to be fluidly coupled to lungs of the patient. Exhaled gas from the patient is transmitted from patient interface 34 to expiratory port 32.
  • Expiratory port 32 is fluidly coupled to expiratory conduit 26, which transmits exhaled gas back to ventilator 12.
  • patient interface 34 is an endotracheal tube. Other patient interfaces can include masks, nasal prongs, etc.
  • ventilator 12 includes a controller 40 for operating the ventilator
  • controller 40 can provide several functions to monitor and control various parameters associated with respiratory therapy system 10. Such parameters include gas flow rate, gas temperature, carbon dioxide quantity, gas mixture percentages, etc.
  • ventilator 12 includes an air inlet 42 and a gas inlet 44 fluidly coupled to a gas mixing and flow delivery module 46.
  • controller 40 is configured to control gas mixing and flow delivery module 46 so as to provide a desired gas mixture to initial conduit 20.
  • Air inlet 42 provides air to gas mixing and flow delivery module 46 whereas gas inlet 44 provides a gas such as oxygen to gas mixing and flow delivery module 46.
  • Gas mixing and flow delivery module 46 mixes the gases from inlets 42 and 44 in order to provide a desired blend of gas.
  • ventilator 12 may operate solely with air, with a predetermined mixture of gas (e.g., a mixture of helium and oxygen) or operate with other gas inlet configurations.
  • a predetermined mixture of gas e.g., a mixture of helium and oxygen
  • the desired blend of gas from mixing and flow delivery module 46 flows through a flow sensor 48 and a pressure sensor 50, which monitor the flow and pressure, respectively, of gas flowing to initial conduit 20.
  • Flow sensor 48 and pressure sensor 50 can be coupled to controller 40 so as to provide data to controller 40 for control of ventilator 12.
  • Initial conduit 20 is fluidly coupled to ventilator 12 at a gas outlet 52.
  • ventilator 12 also receives exhaled air from the patient through expiratory port 32 and expiratory conduit 26, which can be fluidly coupled to ventilator 12 through a gas inlet 54.
  • exhaled gas flows through a flow sensor 56 and a carbon dioxide sensor 58 to an exhaust valve 60, which can both be operably coupled to controller 40.
  • Exhaust valve 60 can be operated to release gas from ventilator 12 through an exhaust 62 so as to maintain a desired pressure within patient circuit 16.
  • Flow sensor 56 measures flow of air from the patient while carbon dioxide sensor 58 determines whether the patient circuit 16 is properly coupled to the patient, for example by comparing an amount of carbon dioxide in the exhaled air to a threshold.
  • Carbon dioxide sensor 58 can be obtained from Alphasense Ltd., of Great Notley, United Kingdom, part IRC-A1, in one embodiment. In any event, the carbon dioxide sensor is fluidly coupled to expiratory port 32 so as to measure an amount of carbon dioxide from the patient.
  • a carbon dioxide sensor need not be positioned directly within ventilator 12 and can be selectively positioned in various locations so as to be fluidly coupled to an expiratory port and receive exhaled gas from the patient.
  • multiple carbon dioxide sensors can be utilized in other embodiments.
  • a first carbon dioxide sensor 70 is positioned proximate the patient and fluidly coupled directly to expiratory port 32 and y-connector 24, the carbon dioxide 70 sensor being electrically coupled to the ventilator 12 through a cable 72.
  • Carbon dioxide sensor 70 measures an amount of carbon dioxide in expiratory port 32 and provides the amount to ventilator 12.
  • the carbon dioxide sensor 70 can be coupled to controller 40.
  • a second carbon dioxide sensor 74 is fluidly coupled to inspiratory port 28 to measure an amount of carbon dioxide in the inspiratory port 28. The respective measured values from sensors 70 and 74 can be compared by controller 40 to determine whether the patient circuit 16 is fluidly coupled to the patient.
  • a flow sensor 80 and a carbon dioxide sensor 82 are both fluidly coupled to expiratory port 32 proximate the patient.
  • the carbon dioxide sensor 82 is coupled with the flow sensor 80 and measurements from the flow sensor 80 and carbon dioxide sensor 82 are provided to ventilator 12, and in particular controller 40, through a cable 84.
  • patient interface 34 is embodied as a mask 90, wherein a carbon dioxide sensor 92 is directly affixed to the mask 90 and electrically coupled to ventilator 12 though a cable 94. Expiratory conduit 26 has been eliminated and exhaled gas is released from the mask 90 through an expiratory port integrated into the mask 90. Carbon dioxide sensor 92 directly measures an amount of carbon dioxide exhaled by the patient into the mask 90.
  • FIG. 5 is a close-up view of mask 90, illustrating carbon dioxide sensor 92 and cable 94 coupled thereto. Carbon dioxide sensor is provided in an expiratory port 95 of mask 90.
  • Mask 90 also includes a safety valve 96 for releasing pressure within mask 90.
  • a photochemical carbon dioxide sensor 98 can provide further visual indication of mask 90 being fluidly coupled to the patient.
  • system 10 By fluidly coupling a carbon dioxide detector to an expiratory port, system 10, as illustrated in FIGS. 1-4 above, can detect if a patient interface is fluidly coupled to a patient.
  • Exhaled gas from a patient includes higher amounts of carbon dioxide then ambient gas or inhaled gas within inspiratory conduit 22.
  • a carbon dioxide sensor e.g., sensors 58, 70, 74, 82, 92
  • a non-dispersive infrared sensor or electrochemical sensor to analyze exhaled gas can detect presence or absence of carbon dioxide in order to provide a reliable detection for a loss of breathing circuit integrity. Stated another way, a low level of carbon dioxide for a period of time can indicate that a patient interface is not properly fluidly coupled to the patient.
  • the carbon dioxide concentration in the exhaled gas is measured by the carbon dioxide sensor and continuously compared with a threshold value.
  • the alarm 64 e.g., audible and/or visible
  • the alarm can include a red flashing lamp, an audible alarm, a textual message provided on a graphical interface and/or combinations thereof.
  • a differential value can be calculated between different carbon dioxide measurements. The differential value can further be compared to a threshold and alarm 64 operated if the value is below the threshold.
  • a photochemical carbon dioxide detector e.g., sensor 98
  • FIG. 6 is a graph of an amount carbon dioxide measured as a function of time. In periods where the patient exhales, as denoted by period 100, the amount of carbon dioxide rises. In contrast, where the patient inhales, as denoted by period 102, the amount of carbon dioxide is reduced to a small amount. In some instances, it may be appropriate to use a fixed threshold carbon dioxide concentration, for example, within a range of 1,000 to 10,000 parts per million. An example threshold 104 is indicated in FIG. 6. One example threshold would be 1,500 parts per million (i.e., 0.15%). In other applications, an algorithm may be used to select a preferred threshold value.
  • a preferred threshold may be selected within the same range, allowing more rapid detection of disconnection.
  • the value for a specified period for detection of disconnection may either be a preset preferred value, such as 30 seconds or it may be longer or shorter and determined by a clinician using knowledge of a patient's physiological status. For example, a shorter interval such as 10 seconds may be appropriate in the case of a pre-term infant, who may sustain significant harm within 20 seconds of loss of respiratory support, or the value may be at longer intervals such as one minute for an adult patient requiring some additional support for spontaneous breathing.

Abstract

A carbon dioxide sensor for use in a respiratory therapy system. The carbon dioxide sensor determines whether a patient interface is fluidly coupled to a patient.

Description

PATIENT CIRCUIT INTEGRITY ALARM USING EXHALED C02
Background
[01] Lung ventilators provide therapeutic gas (e.g., oxygen) and pressure volume support to a patient's lungs in order to facilitate gas exchange with a patient, either by supporting spontaneous breathing or by providing mandatory ventilation in the absence of spontaneous breathing. The gas is provided to a patient through an inspiratory conduit and the ventilator is fluidly coupled to the lung using a patient interface such as an endotracheal tube, a nasal cannula or a mask. There is a risk that fluid connection from the ventilator to the lung may be lost, for example due to movement of the patient causing the patient interface to become dislodged. If the patient interface is disconnected from the patient, this loss of breathing can be harmful to the patient.
[02] Current ventilators detect such loss of breathing by use of complex algorithms based on measurements of breathing circuit pressure and flow. These algorithms can be problematic in scenarios with significant leaks, such as are common in long term applications, or with high-resistance tubes such as narrow bore nasal cannulae. When a breathing tube is dislodged, it may remain occluded or partially occluded, for example, by resting against the patient's face, causing the alarm mechanism to fail. Still further, these complex algorithms can be difficult to implement within the ventilator. As a result, reliable detection methods and adequate sensitivity to breathing circuit integrity are desired.
Summary
[03] The present disclosure relates to a use of a carbon dioxide sensor to indicate whether a patient circuit is in fluid connection with a patient's lungs. In one aspect, a respiratory therapy system includes an inspiratory conduit and an expiratory port. A patient interface is fluidly coupled to the inspiratory conduit and the expiratory port. The patient interface is further configured to be coupled to a patient. A carbon dioxide sensor is fluidly coupled to the expiratory port and provides an indication of whether the patient interface is fluidly coupled to the patient. [04] In another aspect, a respiratory therapy system includes a ventilator configured to provide inhaled gas to a patient and receive exhaled gas from the patient. The respiratory therapy system also includes a carbon dioxide sensor determining an amount of carbon dioxide in the exhaled gas and comparing the amount to a threshold.
[05] In yet another aspect, a method of providing respiratory therapy to a patient includes providing a patient interface configured to be fluidly coupled to the patient. Gas is provided to the patient interface through an inspiratory conduit and exhaled gas is received from the patient. An amount of carbon dioxide is measured in the exhaled gas and an indication of fluid coupling between the patient interface and the patient is provided as a function of the amount of carbon dioxide.
Brief Description of the Drawings [06] FIG. 1 is a schematic diagram of a first embodiment of a respiratory therapy system.
[07] FIG. 2 is a schematic diagram of a second embodiment of a respiratory therapy system.
[08] FIG 3. is a schematic diagram of a third embodiment of a respiratory therapy system.
[09] FIG. 4 is a schematic diagram of a fourth embodiment of a respiratory therapy system.
[10] FIG. 5 is a schematic diagram of a mask having a carbon dioxide sensor coupled thereto.
[11] FIG. 6 is a graph of carbon dioxide measured from exhaled gas of a respiratory therapy system as a function of time.
Detailed Description
[12] FIG. 1 is a schematic view of a respiratory therapy system 10 including a ventilator
12, an optional humidifier 14 and a patient circuit 16. It is worth noting that system 10 is one exemplary embodiment for concepts presented herein. For example, other forms of respiratory therapy can be used with the concepts presented herein such as a CPAP (Continuous Positive Airway Pressure) System or other system that may add or remove one or more of the components of system 10. In the embodiment illustrated, ventilator 12 supplies gases to humidifier 14 through an initial conduit 20. Humidifier 14 heats water within a humidification chamber to form water vapor, which mixes with gas provided by the ventilator 12, which is then output to patient circuit 16. Patient circuit 16 includes an inspiratory conduit (or limb) 22, a y-connector 24 and an expiratory conduit (or limb) 26. In alternative embodiments, for example, in a CPAP system, the y-connector 24 and/or expiratory conduit 26 can be eliminated. In other embodiments, humidifier 14 can be eliminated and thus the patient is provided with dry breathing gas.
[13] Y-connector 24 includes an inspiratory port 28, a patient port 30 and an expiratory port 32. Inspiratory conduit 22 is fluidly coupled to the inspiratory port 28, so that gases from ventilator 12 are transferred from the inspiratory port 28 to the patient port 30. Patient port 30, in turn, is fluidly coupled to a patient interface 34 that is configured to be fluidly coupled to lungs of the patient. Exhaled gas from the patient is transmitted from patient interface 34 to expiratory port 32. Expiratory port 32 is fluidly coupled to expiratory conduit 26, which transmits exhaled gas back to ventilator 12. In one embodiment, patient interface 34 is an endotracheal tube. Other patient interfaces can include masks, nasal prongs, etc.
[14] In one embodiment, ventilator 12 includes a controller 40 for operating the ventilator
12. For example, the controller 40 can provide several functions to monitor and control various parameters associated with respiratory therapy system 10. Such parameters include gas flow rate, gas temperature, carbon dioxide quantity, gas mixture percentages, etc. Additionally, ventilator 12 includes an air inlet 42 and a gas inlet 44 fluidly coupled to a gas mixing and flow delivery module 46. In one embodiment, controller 40 is configured to control gas mixing and flow delivery module 46 so as to provide a desired gas mixture to initial conduit 20. Air inlet 42 provides air to gas mixing and flow delivery module 46 whereas gas inlet 44 provides a gas such as oxygen to gas mixing and flow delivery module 46. Gas mixing and flow delivery module 46 mixes the gases from inlets 42 and 44 in order to provide a desired blend of gas. In other embodiments, ventilator 12 may operate solely with air, with a predetermined mixture of gas (e.g., a mixture of helium and oxygen) or operate with other gas inlet configurations. The desired blend of gas from mixing and flow delivery module 46 flows through a flow sensor 48 and a pressure sensor 50, which monitor the flow and pressure, respectively, of gas flowing to initial conduit 20. Flow sensor 48 and pressure sensor 50 can be coupled to controller 40 so as to provide data to controller 40 for control of ventilator 12. Initial conduit 20 is fluidly coupled to ventilator 12 at a gas outlet 52.
[15] In one embodiment, ventilator 12 also receives exhaled air from the patient through expiratory port 32 and expiratory conduit 26, which can be fluidly coupled to ventilator 12 through a gas inlet 54. After entering ventilator 12, exhaled gas flows through a flow sensor 56 and a carbon dioxide sensor 58 to an exhaust valve 60, which can both be operably coupled to controller 40. Exhaust valve 60 can be operated to release gas from ventilator 12 through an exhaust 62 so as to maintain a desired pressure within patient circuit 16. Flow sensor 56 measures flow of air from the patient while carbon dioxide sensor 58 determines whether the patient circuit 16 is properly coupled to the patient, for example by comparing an amount of carbon dioxide in the exhaled air to a threshold. If the amount of carbon dioxide is below the threshold for a period of time, an alarm 64 can be operated (e.g., by controller 40). Carbon dioxide sensor 58 can be obtained from Alphasense Ltd., of Great Notley, United Kingdom, part IRC-A1, in one embodiment. In any event, the carbon dioxide sensor is fluidly coupled to expiratory port 32 so as to measure an amount of carbon dioxide from the patient.
[16] It is worth noting that in other embodiments, a carbon dioxide sensor need not be positioned directly within ventilator 12 and can be selectively positioned in various locations so as to be fluidly coupled to an expiratory port and receive exhaled gas from the patient. Moreover, multiple carbon dioxide sensors can be utilized in other embodiments. In one example illustrated in FIG. 2, a first carbon dioxide sensor 70 is positioned proximate the patient and fluidly coupled directly to expiratory port 32 and y-connector 24, the carbon dioxide 70 sensor being electrically coupled to the ventilator 12 through a cable 72. Carbon dioxide sensor 70 measures an amount of carbon dioxide in expiratory port 32 and provides the amount to ventilator 12. In one embodiment, the carbon dioxide sensor 70 can be coupled to controller 40. A second carbon dioxide sensor 74 is fluidly coupled to inspiratory port 28 to measure an amount of carbon dioxide in the inspiratory port 28. The respective measured values from sensors 70 and 74 can be compared by controller 40 to determine whether the patient circuit 16 is fluidly coupled to the patient. [17] In another embodiment, illustrated in FIG. 3, a flow sensor 80 and a carbon dioxide sensor 82 are both fluidly coupled to expiratory port 32 proximate the patient. The carbon dioxide sensor 82 is coupled with the flow sensor 80 and measurements from the flow sensor 80 and carbon dioxide sensor 82 are provided to ventilator 12, and in particular controller 40, through a cable 84.
[18] In yet a further embodiment, illustrated in FIG. 4, patient interface 34 is embodied as a mask 90, wherein a carbon dioxide sensor 92 is directly affixed to the mask 90 and electrically coupled to ventilator 12 though a cable 94. Expiratory conduit 26 has been eliminated and exhaled gas is released from the mask 90 through an expiratory port integrated into the mask 90. Carbon dioxide sensor 92 directly measures an amount of carbon dioxide exhaled by the patient into the mask 90. FIG. 5 is a close-up view of mask 90, illustrating carbon dioxide sensor 92 and cable 94 coupled thereto. Carbon dioxide sensor is provided in an expiratory port 95 of mask 90. Mask 90 also includes a safety valve 96 for releasing pressure within mask 90. In a further embodiment, a photochemical carbon dioxide sensor 98 can provide further visual indication of mask 90 being fluidly coupled to the patient.
[19] By fluidly coupling a carbon dioxide detector to an expiratory port, system 10, as illustrated in FIGS. 1-4 above, can detect if a patient interface is fluidly coupled to a patient. Exhaled gas from a patient includes higher amounts of carbon dioxide then ambient gas or inhaled gas within inspiratory conduit 22. Using a carbon dioxide sensor (e.g., sensors 58, 70, 74, 82, 92), for example a non-dispersive infrared sensor or electrochemical sensor, to analyze exhaled gas can detect presence or absence of carbon dioxide in order to provide a reliable detection for a loss of breathing circuit integrity. Stated another way, a low level of carbon dioxide for a period of time can indicate that a patient interface is not properly fluidly coupled to the patient. In one embodiment, the carbon dioxide concentration in the exhaled gas is measured by the carbon dioxide sensor and continuously compared with a threshold value. In the event that the concentration remains below a threshold value for a specified period of time, the alarm 64 (e.g., audible and/or visible) is operated to alert the caregiver. In one example, the alarm can include a red flashing lamp, an audible alarm, a textual message provided on a graphical interface and/or combinations thereof. If multiple carbon dioxide sensors are used (e.g., sensors 70 and 74) a differential value can be calculated between different carbon dioxide measurements. The differential value can further be compared to a threshold and alarm 64 operated if the value is below the threshold. In a further embodiment, a photochemical carbon dioxide detector (e.g., sensor 98) can be used to provide further visual indication of a patient interface being fluidly coupled to a patient's lungs.
[20] FIG. 6 is a graph of an amount carbon dioxide measured as a function of time. In periods where the patient exhales, as denoted by period 100, the amount of carbon dioxide rises. In contrast, where the patient inhales, as denoted by period 102, the amount of carbon dioxide is reduced to a small amount. In some instances, it may be appropriate to use a fixed threshold carbon dioxide concentration, for example, within a range of 1,000 to 10,000 parts per million. An example threshold 104 is indicated in FIG. 6. One example threshold would be 1,500 parts per million (i.e., 0.15%). In other applications, an algorithm may be used to select a preferred threshold value. For example, when a size of the patient or a tidal volume of the patient is known and the biased flow rate (e.g., the flow rate of fresh breathing gas through the circuit during isolation, and intended to sweep exhaled gas from the circuit to prevent rebreathing) is known, a preferred threshold may be selected within the same range, allowing more rapid detection of disconnection.
[21] The value for a specified period for detection of disconnection may either be a preset preferred value, such as 30 seconds or it may be longer or shorter and determined by a clinician using knowledge of a patient's physiological status. For example, a shorter interval such as 10 seconds may be appropriate in the case of a pre-term infant, who may sustain significant harm within 20 seconds of loss of respiratory support, or the value may be at longer intervals such as one minute for an adult patient requiring some additional support for spontaneous breathing.
[22] In any event, in cases where the patient interface (e.g., tubing, cannula or mask) falls out of the patient's orifice and becomes partially blocked or occluded, detection of the leak can be provided by the carbon dioxide sensor. Additionally, by monitoring carbon dioxide, other highly dangerous situations such as obstruction of the trachea or main bronchus in a patient, cardiac arrest, etc., will also operate the alarm 64.
[23] Although the present disclosure has been described with reference to preferred embodiments, workers skilled in the art will recognize that changes can be made in form and detail without departing from the spirit and scope of the present disclosure.

Claims

What is claimed is:
1. A respiratory therapy system, comprising:
an inspiratory conduit;
an expiratory port;
a patient interface fluidly coupled to the inspiratory conduit and the expiratory port, the patient interface configured to be fluidly coupled to a patient; and a carbon dioxide sensor fluidly coupled to the expiratory port and providing an indication of whether the patient interface is fluidly coupled to the patient.
2. The respiratory therapy system of claim 1, wherein the carbon dioxide sensor measures an amount of carbon dioxide and compares the amount to a threshold.
3. The respiratory therapy system of claim 1, wherein the carbon dioxide sensor is connected to the patient interface.
4. The respiratory therapy system of claim 1, wherein the carbon dioxide sensor is connected to the expiratory port.
5. The respiratory therapy system of claim 1, further comprising:
a ventilator providing gas to the inspiratory conduit and receiving exhaled gas from the expiratory port through an expiratory conduit, wherein the carbon dioxide sensor is connected to the ventilator.
6. The respiratory therapy system of claim 1, further comprising:
a second carbon dioxide sensor, wherein the first-mentioned carbon dioxide sensor is configured to determine a first amount of carbon dioxide in a first gas and the second carbon dioxide sensor determines a second amount of carbon dioxide in a second gas, the first-mentioned carbon dioxide sensor comparing the first amount to the second amount to provide the indication.
7. The respiratory therapy system of claim 1 , further comprising: an alarm coupled to the carbon dioxide sensor and configured to be operated if the carbon dioxide sensor provides an indication that the patient interface is not fluidly coupled to the patient.
8. A respiratory therapy system, comprising:
a ventilator configured to provide inhaled gas to a patient and receive exhaled gas from the patient; and
a carbon dioxide sensor determining an amount of carbon dioxide in the exhaled gas and compare the amount to a threshold.
9. The respiratory therapy system of claim 8, further comprising:
an inspiratory conduit;
an expiratory port;
a patient interface fluidly coupled to the inspiratory conduit and the expiratory port, the patient interface configured to be fluidly coupled to a patient; and wherein the carbon dioxide sensor provides an indication of whether the patient interface is fluidly coupled to the patient.
10. The respiratory therapy system of claim 9, wherein the carbon dioxide sensor is connected to the patient interface.
11. The respiratory therapy system of claim 9, wherein the carbon dioxide sensor is connected to the expiratory port.
12. The respiratory therapy system of claim 8, wherein the carbon dioxide sensor is connected to the ventilator.
13. The respiratory therapy system of claim 8, further comprising:
a second carbon dioxide sensor, wherein the first-mentioned carbon dioxide sensor is configured to determine a first amount of carbon dioxide in a first gas and the second carbon dioxide sensor deterrnines a second amount of carbon dioxide in a second gas, the first-mentioned carbon dioxide sensor comparing the first amount to the second amount to determine a difference and compare the difference to a threshold.
14. The respiratory therapy system of claim 8, further comprising:
an alarm coupled to the carbon dioxide sensor and configured to be operated if the carbon dioxide sensor provides an indication if the amount of carbon dioxide is below the threshold.
15. A method of providing respiratory therapy to a patient, comprising:
providing a patient interface configured to be coupled to the patient;
providing gas to the patient interface;
receiving exhaled gas from the patient;
measuring an amount of carbon dioxide in the exhaled gas; and
providing an indication of fluid coupling between the patient interface and the patient as a function of the amount of carbon dioxide.
16. The method of claim 15, wherein providing the indication further includes comparing the amount to a threshold.
17. The method of claim 15, further comprising:
providing a carbon dioxide sensor connected to the patient interface.
18. The method of claim 15, further comprising:
measuring a second amount of carbon dioxide in a gas other than the exhaled gas; comparing the first-mentioned amount to the second amount; and
determining if the patient interface is fluidly coupled to the patient as a function of the comparison.
19. The method of claim 15, further comprising:
operating an alarm if the patient interface is not fluidly coupled to the patient.
PCT/US2011/035899 2010-05-11 2011-05-10 Patient circuit integrity alarm using exhaled c02 WO2011143198A2 (en)

Priority Applications (4)

Application Number Priority Date Filing Date Title
MX2012012791A MX2012012791A (en) 2010-05-11 2011-05-10 Patient circuit integrity alarm using exhaled c02.
EP11781131.5A EP2569036B1 (en) 2010-05-11 2011-05-10 Patient circuit integrity alarm using exhaled c02
CN201180023261.XA CN103002939B (en) 2010-05-11 2011-05-10 Utilize patient's circuit integrity alarm of the carbon dioxide of breathing out
BR112012028156-9A BR112012028156B1 (en) 2010-05-11 2011-05-10 respiratory therapy system

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US12/777,393 2010-05-11
US12/777,393 US8905019B2 (en) 2010-05-11 2010-05-11 Patient circuit integrity alarm using exhaled CO2

Publications (2)

Publication Number Publication Date
WO2011143198A2 true WO2011143198A2 (en) 2011-11-17
WO2011143198A3 WO2011143198A3 (en) 2012-04-05

Family

ID=44910635

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/US2011/035899 WO2011143198A2 (en) 2010-05-11 2011-05-10 Patient circuit integrity alarm using exhaled c02

Country Status (6)

Country Link
US (1) US8905019B2 (en)
EP (1) EP2569036B1 (en)
CN (1) CN103002939B (en)
BR (1) BR112012028156B1 (en)
MX (1) MX2012012791A (en)
WO (1) WO2011143198A2 (en)

Families Citing this family (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20120272962A1 (en) * 2011-04-29 2012-11-01 Nellcor Puritan Bennett Llc Methods and systems for managing a ventilator patient with a capnometer
GB2510321B (en) * 2012-11-12 2018-01-31 Biosurgical S L Agitation apparatus
CA2889825C (en) * 2014-04-30 2023-11-07 Maurizio Borsari Process and apparatus for the detection of the concentration and/or amount of carbon dioxide per unit of time contained in a flow of gas to be monitored
WO2016103122A1 (en) * 2014-12-24 2016-06-30 Koninklijke Philips N.V. Systems and methods for detection of ventilator and patient disconnections using patient lung compliance estimated on both inhalation and exhalation phases of a breath
EP3302267A4 (en) * 2015-06-03 2019-01-16 The Regents of the University of California Resuscitation and ventilation monitor
DE102017124256A1 (en) * 2016-10-29 2018-05-03 Sendsor Gmbh Sensor and method for measuring the properties of the respiratory gas
CN109718449B (en) * 2018-12-29 2020-04-10 北京谊安医疗系统股份有限公司 Prompting method and system in anesthesia induction process and respiratory support machine
US20210128863A1 (en) * 2019-06-10 2021-05-06 Neotech Products Llc Nasal cannula and tubing with ventilator system
WO2022119790A1 (en) * 2020-12-01 2022-06-09 The Government Of The United States, As Represented By The Secretary Of The Army Thermogenic airway management device and methods

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6041777A (en) * 1995-12-01 2000-03-28 Alliance Pharmaceutical Corp. Methods and apparatus for closed-circuit ventilation therapy
US20050177055A1 (en) * 2000-02-22 2005-08-11 Kai Kuck Algorithms, systems, and methods for estimating carbon dioxide stores, transforming respiratory gas measurements, and obtaining accurate noninvasive pulmonary capillary blood flow and cardiac output measurements
US20050203432A1 (en) * 1996-12-19 2005-09-15 Orr Joseph A. Apparatus and method for non-invasively measuring cardiac output
US20070028921A1 (en) * 1999-06-30 2007-02-08 Banner Michael J Medical ventilator and method of controlling same

Family Cites Families (21)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4302640A (en) 1979-11-07 1981-11-24 Bourns Medical Systems, Inc. Flow detector
US5063938A (en) * 1990-11-01 1991-11-12 Beck Donald C Respiration-signalling device
US5319355A (en) * 1991-03-06 1994-06-07 Russek Linda G Alarm for patient monitor and life support equipment system
JPH0620535Y2 (en) * 1991-07-08 1994-06-01 アトム株式会社 Airway adapter
US5662099A (en) 1996-03-29 1997-09-02 Ohmeda Inc. Detection of bellows collapsed condition in medical ventilator
DK0973443T3 (en) * 1997-01-17 2006-07-24 Ino Therapeutics Gmbh Controlled gas supply system
US5881717A (en) * 1997-03-14 1999-03-16 Nellcor Puritan Bennett Incorporated System and method for adjustable disconnection sensitivity for disconnection and occlusion detection in a patient ventilator
AUPP783198A0 (en) * 1998-12-21 1999-01-21 Resmed Limited Determination of mask fitting pressure and correct mask fit
IL130371A (en) * 1999-06-08 2004-06-01 Oridion Medical Ltd Capnography waveform interpreter
US6938619B1 (en) * 2000-06-13 2005-09-06 Scott Laboratories, Inc. Mask free delivery of oxygen and ventilatory monitoring
EP1322367A4 (en) * 2000-09-28 2009-08-26 Invacare Corp Carbon dioxide-based bi-level cpap control
US7886740B2 (en) * 2003-01-28 2011-02-15 Beth Israel Deaconess Medical Center, Inc. Gas systems and methods for enabling respiratory stability
US7343917B2 (en) * 2003-09-22 2008-03-18 Resmed Limited Clear cycle for ventilation device
WO2005113045A1 (en) * 2004-04-20 2005-12-01 Crutchfield Clifton D Respirator fit-testing apparatus and method
JP5053083B2 (en) * 2004-06-24 2012-10-17 コンヴァージェント エンジニアリング インコーポレイティッド Method and apparatus for non-invasive prediction of positive end expiratory pressure (PEEPi) in a patient receiving ventilator support
EP1820528A1 (en) 2006-02-20 2007-08-22 General Electric Company Patient breathing circuit
GB0607939D0 (en) * 2006-04-21 2006-05-31 Imp College Innovations Ltd Method and device for stabilising disordered breathing
US8312879B2 (en) * 2006-10-16 2012-11-20 General Electric Company Method and apparatus for airway compensation control
CA2668055A1 (en) * 2006-11-01 2008-05-08 Joseph Fisher Portable life support apparatus
CN201286922Y (en) * 2008-10-07 2009-08-12 胡战兵 Oxygen absorption tube with respiration monitoring function
JP5758875B2 (en) * 2009-04-02 2015-08-05 ブリーズ・テクノロジーズ・インコーポレーテッド Non-invasive ventilation system

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6041777A (en) * 1995-12-01 2000-03-28 Alliance Pharmaceutical Corp. Methods and apparatus for closed-circuit ventilation therapy
US20050203432A1 (en) * 1996-12-19 2005-09-15 Orr Joseph A. Apparatus and method for non-invasively measuring cardiac output
US20070028921A1 (en) * 1999-06-30 2007-02-08 Banner Michael J Medical ventilator and method of controlling same
US20050177055A1 (en) * 2000-02-22 2005-08-11 Kai Kuck Algorithms, systems, and methods for estimating carbon dioxide stores, transforming respiratory gas measurements, and obtaining accurate noninvasive pulmonary capillary blood flow and cardiac output measurements

Also Published As

Publication number Publication date
CN103002939A (en) 2013-03-27
BR112012028156B1 (en) 2020-12-01
WO2011143198A3 (en) 2012-04-05
US8905019B2 (en) 2014-12-09
EP2569036A4 (en) 2017-08-09
EP2569036B1 (en) 2020-12-09
EP2569036A2 (en) 2013-03-20
BR112012028156A2 (en) 2016-12-06
MX2012012791A (en) 2013-05-20
CN103002939B (en) 2016-01-20
US20110277758A1 (en) 2011-11-17

Similar Documents

Publication Publication Date Title
EP2569036B1 (en) Patient circuit integrity alarm using exhaled c02
US20210308395A1 (en) System for determining airway patency
JP7067925B2 (en) System and method for advanced gas sources and / or therapeutic gas supply system and method and / or therapeutic gas supply augmentation performance verification
US8033280B2 (en) Inhalation anaesthesia delivery system and a method for leak detection in the inhalation anaesthesia delivery system
US20200360634A1 (en) Endotracheal tube extubation detection
US6668828B1 (en) System and elements for managing therapeutic gas administration to a spontaneously breathing non-ventilated patient
US20080295837A1 (en) Method to limit leak compensation based on a breathing circuit leak alarm
US20050217668A1 (en) System and elements for managing therapeutic gas administration to a spontaneously breathing non-ventilated patient
EP2383008B1 (en) Arrangement for maintaining volume of breathing gas in a desired level
JP5570853B2 (en) Ventilator
JP2017509432A (en) System and method for delivering therapeutic gas to a patient in need using enhanced breathing circuit gas (BCG) flow measurement
EP2914321B1 (en) A breathing apparatus and a method therein
US20180256837A1 (en) Gas flow indicator
US10821247B2 (en) Ventilator and operating method for a ventilator with a determination of cough attacks
CN105944201B (en) A kind of medicinal intelligent ventilator
US20240075226A1 (en) System and method for accurate estimation of intentional and unintentional leaks in flow generation systems
US8973575B2 (en) Anaesthesia machine arrangement and a method in connection with an anaesthesia machine arrangement
US11135382B2 (en) Medical device and process for alarm organization
CN114364422A (en) Supplemental gas source detection and related apparatus and methods
CN204017086U (en) No supply and monitoring device and respiratory system
CN108066865B (en) Medical device and method for determining an operating situation in a medical device
WO2020081394A1 (en) Improved continuous positive airway pressure device for neonates
WO2021240529A1 (en) Ventilation splitter device and system and method for ventilation
US20110209703A1 (en) Artificial ventilation apparatus
KR20240006502A (en) Alarm for respiratory assistance systems

Legal Events

Date Code Title Description
WWE Wipo information: entry into national phase

Ref document number: 201180023261.X

Country of ref document: CN

121 Ep: the epo has been informed by wipo that ep was designated in this application

Ref document number: 11781131

Country of ref document: EP

Kind code of ref document: A2

WWE Wipo information: entry into national phase

Ref document number: MX/A/2012/012791

Country of ref document: MX

WWE Wipo information: entry into national phase

Ref document number: 2011781131

Country of ref document: EP

NENP Non-entry into the national phase

Ref country code: DE

REG Reference to national code

Ref country code: BR

Ref legal event code: B01A

Ref document number: 112012028156

Country of ref document: BR

ENP Entry into the national phase

Ref document number: 112012028156

Country of ref document: BR

Kind code of ref document: A2

Effective date: 20121101