EP3962612A1 - Appareil d'exercice respiratoire - Google Patents

Appareil d'exercice respiratoire

Info

Publication number
EP3962612A1
EP3962612A1 EP20723374.3A EP20723374A EP3962612A1 EP 3962612 A1 EP3962612 A1 EP 3962612A1 EP 20723374 A EP20723374 A EP 20723374A EP 3962612 A1 EP3962612 A1 EP 3962612A1
Authority
EP
European Patent Office
Prior art keywords
air
mouthpiece
branch
valve
training device
Prior art date
Legal status (The legal status 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 status listed.)
Pending
Application number
EP20723374.3A
Other languages
German (de)
English (en)
Inventor
Christina SPENGLER
Corina SCHAER
Diego Stutzer
Damien MAURER
Adrian SALLAZ
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Idiag
Original Assignee
Idiag
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 Idiag filed Critical Idiag
Publication of EP3962612A1 publication Critical patent/EP3962612A1/fr
Pending legal-status Critical Current

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
    • A61M16/0057Pumps therefor
    • A61M16/0078Breathing bags
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B5/00Measuring for diagnostic purposes; Identification of persons
    • A61B5/08Detecting, measuring or recording devices for evaluating the respiratory organs
    • A61B5/083Measuring rate of metabolism by using breath test, e.g. measuring rate of oxygen consumption
    • A61B5/0836Measuring rate of CO2 production
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B5/00Measuring for diagnostic purposes; Identification of persons
    • A61B5/08Detecting, measuring or recording devices for evaluating the respiratory organs
    • A61B5/087Measuring breath flow
    • A61B5/0878Measuring breath flow using temperature sensing means
    • 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
    • A61M16/0006Accessories therefor, e.g. sensors, vibrators, negative pressure with means for creating vibrations in patients' airways
    • 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
    • A61M16/0045Means for re-breathing exhaled gases, e.g. for hyperventilation treatment
    • 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
    • A61M16/08Bellows; Connecting tubes ; Water traps; Patient circuits
    • A61M16/0866Passive resistors therefor
    • 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
    • A61M16/20Valves specially adapted to medical respiratory devices
    • A61M16/201Controlled valves
    • A61M16/202Controlled valves electrically actuated
    • A61M16/203Proportional
    • A61M16/204Proportional used for inhalation control
    • 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
    • A61M16/203Proportional
    • A61M16/205Proportional used for exhalation control
    • AHUMAN NECESSITIES
    • A63SPORTS; GAMES; AMUSEMENTS
    • A63BAPPARATUS FOR PHYSICAL TRAINING, GYMNASTICS, SWIMMING, CLIMBING, OR FENCING; BALL GAMES; TRAINING EQUIPMENT
    • A63B21/00Exercising apparatus for developing or strengthening the muscles or joints of the body by working against a counterforce, with or without measuring devices
    • A63B21/00196Exercising apparatus for developing or strengthening the muscles or joints of the body by working against a counterforce, with or without measuring devices using pulsed counterforce, e.g. vibrating resistance means
    • AHUMAN NECESSITIES
    • A63SPORTS; GAMES; AMUSEMENTS
    • A63BAPPARATUS FOR PHYSICAL TRAINING, GYMNASTICS, SWIMMING, CLIMBING, OR FENCING; BALL GAMES; TRAINING EQUIPMENT
    • A63B21/00Exercising apparatus for developing or strengthening the muscles or joints of the body by working against a counterforce, with or without measuring devices
    • A63B21/008Exercising apparatus for developing or strengthening the muscles or joints of the body by working against a counterforce, with or without measuring devices using hydraulic or pneumatic force-resisters
    • AHUMAN NECESSITIES
    • A63SPORTS; GAMES; AMUSEMENTS
    • A63BAPPARATUS FOR PHYSICAL TRAINING, GYMNASTICS, SWIMMING, CLIMBING, OR FENCING; BALL GAMES; TRAINING EQUIPMENT
    • A63B21/00Exercising apparatus for developing or strengthening the muscles or joints of the body by working against a counterforce, with or without measuring devices
    • A63B21/008Exercising apparatus for developing or strengthening the muscles or joints of the body by working against a counterforce, with or without measuring devices using hydraulic or pneumatic force-resisters
    • A63B21/0085Exercising apparatus for developing or strengthening the muscles or joints of the body by working against a counterforce, with or without measuring devices using hydraulic or pneumatic force-resisters using pneumatic force-resisters
    • AHUMAN NECESSITIES
    • A63SPORTS; GAMES; AMUSEMENTS
    • A63BAPPARATUS FOR PHYSICAL TRAINING, GYMNASTICS, SWIMMING, CLIMBING, OR FENCING; BALL GAMES; TRAINING EQUIPMENT
    • A63B23/00Exercising apparatus specially adapted for particular parts of the body
    • A63B23/18Exercising apparatus specially adapted for particular parts of the body for improving respiratory function
    • AHUMAN NECESSITIES
    • A63SPORTS; GAMES; AMUSEMENTS
    • A63BAPPARATUS FOR PHYSICAL TRAINING, GYMNASTICS, SWIMMING, CLIMBING, OR FENCING; BALL GAMES; TRAINING EQUIPMENT
    • A63B24/00Electric or electronic controls for exercising apparatus of preceding groups; Controlling or monitoring of exercises, sportive games, training or athletic performances
    • A63B24/0087Electric or electronic controls for exercising apparatus of groups A63B21/00 - A63B23/00, e.g. controlling load
    • 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
    • A61M16/0057Pumps therefor
    • 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
    • A61M16/0841Joints or connectors for sampling
    • A61M16/085Gas sampling
    • 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
    • A61M16/0841Joints or connectors for sampling
    • A61M16/0858Pressure sampling ports
    • 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
    • A61M16/0003Accessories 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
    • A61M16/10Preparation 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
    • A61M2205/33Controlling, regulating or measuring
    • A61M2205/3331Pressure; Flow
    • A61M2205/3344Measuring or controlling pressure at the body treatment site
    • 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
    • A61M2205/36General characteristics of the apparatus related to heating or cooling
    • A61M2205/3653General characteristics of the apparatus related to heating or cooling by Joule effect, i.e. electric resistance
    • 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
    • A61M2205/50General characteristics of the apparatus with microprocessors or computers
    • A61M2205/502User interfaces, e.g. screens or keyboards
    • A61M2205/505Touch-screens; Virtual keyboard or keypads; Virtual buttons; Soft keys; Mouse touches
    • 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
    • A61M2206/00Characteristics of a physical parameter; associated device therefor
    • A61M2206/10Flow characteristics
    • A61M2206/11Laminar flow
    • 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
    • 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)
    • AHUMAN NECESSITIES
    • A63SPORTS; GAMES; AMUSEMENTS
    • A63BAPPARATUS FOR PHYSICAL TRAINING, GYMNASTICS, SWIMMING, CLIMBING, OR FENCING; BALL GAMES; TRAINING EQUIPMENT
    • A63B24/00Electric or electronic controls for exercising apparatus of preceding groups; Controlling or monitoring of exercises, sportive games, training or athletic performances
    • A63B24/0062Monitoring athletic performances, e.g. for determining the work of a user on an exercise apparatus, the completed jogging or cycling distance
    • A63B2024/0068Comparison to target or threshold, previous performance or not real time comparison to other individuals
    • AHUMAN NECESSITIES
    • A63SPORTS; GAMES; AMUSEMENTS
    • A63BAPPARATUS FOR PHYSICAL TRAINING, GYMNASTICS, SWIMMING, CLIMBING, OR FENCING; BALL GAMES; TRAINING EQUIPMENT
    • A63B24/00Electric or electronic controls for exercising apparatus of preceding groups; Controlling or monitoring of exercises, sportive games, training or athletic performances
    • A63B24/0062Monitoring athletic performances, e.g. for determining the work of a user on an exercise apparatus, the completed jogging or cycling distance
    • A63B2024/0071Distinction between different activities, movements, or kind of sports performed
    • AHUMAN NECESSITIES
    • A63SPORTS; GAMES; AMUSEMENTS
    • A63BAPPARATUS FOR PHYSICAL TRAINING, GYMNASTICS, SWIMMING, CLIMBING, OR FENCING; BALL GAMES; TRAINING EQUIPMENT
    • A63B24/00Electric or electronic controls for exercising apparatus of preceding groups; Controlling or monitoring of exercises, sportive games, training or athletic performances
    • A63B24/0087Electric or electronic controls for exercising apparatus of groups A63B21/00 - A63B23/00, e.g. controlling load
    • A63B2024/0093Electric or electronic controls for exercising apparatus of groups A63B21/00 - A63B23/00, e.g. controlling load the load of the exercise apparatus being controlled by performance parameters, e.g. distance or speed
    • AHUMAN NECESSITIES
    • A63SPORTS; GAMES; AMUSEMENTS
    • A63BAPPARATUS FOR PHYSICAL TRAINING, GYMNASTICS, SWIMMING, CLIMBING, OR FENCING; BALL GAMES; TRAINING EQUIPMENT
    • A63B71/00Games or sports accessories not covered in groups A63B1/00 - A63B69/00
    • A63B71/06Indicating or scoring devices for games or players, or for other sports activities
    • A63B71/0619Displays, user interfaces and indicating devices, specially adapted for sport equipment, e.g. display mounted on treadmills
    • A63B2071/065Visualisation of specific exercise parameters
    • AHUMAN NECESSITIES
    • A63SPORTS; GAMES; AMUSEMENTS
    • A63BAPPARATUS FOR PHYSICAL TRAINING, GYMNASTICS, SWIMMING, CLIMBING, OR FENCING; BALL GAMES; TRAINING EQUIPMENT
    • A63B2220/00Measuring of physical parameters relating to sporting activity
    • A63B2220/50Force related parameters
    • A63B2220/51Force
    • AHUMAN NECESSITIES
    • A63SPORTS; GAMES; AMUSEMENTS
    • A63BAPPARATUS FOR PHYSICAL TRAINING, GYMNASTICS, SWIMMING, CLIMBING, OR FENCING; BALL GAMES; TRAINING EQUIPMENT
    • A63B2220/00Measuring of physical parameters relating to sporting activity
    • A63B2220/50Force related parameters
    • A63B2220/56Pressure
    • AHUMAN NECESSITIES
    • A63SPORTS; GAMES; AMUSEMENTS
    • A63BAPPARATUS FOR PHYSICAL TRAINING, GYMNASTICS, SWIMMING, CLIMBING, OR FENCING; BALL GAMES; TRAINING EQUIPMENT
    • A63B2220/00Measuring of physical parameters relating to sporting activity
    • A63B2220/70Measuring or simulating ambient conditions, e.g. weather, terrain or surface conditions
    • A63B2220/75Humidity
    • AHUMAN NECESSITIES
    • A63SPORTS; GAMES; AMUSEMENTS
    • A63BAPPARATUS FOR PHYSICAL TRAINING, GYMNASTICS, SWIMMING, CLIMBING, OR FENCING; BALL GAMES; TRAINING EQUIPMENT
    • A63B2220/00Measuring of physical parameters relating to sporting activity
    • A63B2220/80Special sensors, transducers or devices therefor
    • A63B2220/83Special sensors, transducers or devices therefor characterised by the position of the sensor
    • A63B2220/833Sensors arranged on the exercise apparatus or sports implement
    • AHUMAN NECESSITIES
    • A63SPORTS; GAMES; AMUSEMENTS
    • A63BAPPARATUS FOR PHYSICAL TRAINING, GYMNASTICS, SWIMMING, CLIMBING, OR FENCING; BALL GAMES; TRAINING EQUIPMENT
    • A63B2225/00Miscellaneous features of sport apparatus, devices or equipment
    • A63B2225/01Special aerodynamic features, e.g. airfoil shapes, wings or air passages
    • AHUMAN NECESSITIES
    • A63SPORTS; GAMES; AMUSEMENTS
    • A63BAPPARATUS FOR PHYSICAL TRAINING, GYMNASTICS, SWIMMING, CLIMBING, OR FENCING; BALL GAMES; TRAINING EQUIPMENT
    • A63B2225/00Miscellaneous features of sport apparatus, devices or equipment
    • A63B2225/64Heated
    • AHUMAN NECESSITIES
    • A63SPORTS; GAMES; AMUSEMENTS
    • A63BAPPARATUS FOR PHYSICAL TRAINING, GYMNASTICS, SWIMMING, CLIMBING, OR FENCING; BALL GAMES; TRAINING EQUIPMENT
    • A63B2230/00Measuring physiological parameters of the user
    • A63B2230/20Measuring physiological parameters of the user blood composition characteristics
    • A63B2230/205P-CO2, i.e. partial CO2 value
    • A63B2230/206P-CO2, i.e. partial CO2 value used as a control parameter for the apparatus
    • AHUMAN NECESSITIES
    • A63SPORTS; GAMES; AMUSEMENTS
    • A63BAPPARATUS FOR PHYSICAL TRAINING, GYMNASTICS, SWIMMING, CLIMBING, OR FENCING; BALL GAMES; TRAINING EQUIPMENT
    • A63B2230/00Measuring physiological parameters of the user
    • A63B2230/40Measuring physiological parameters of the user respiratory characteristics
    • AHUMAN NECESSITIES
    • A63SPORTS; GAMES; AMUSEMENTS
    • A63BAPPARATUS FOR PHYSICAL TRAINING, GYMNASTICS, SWIMMING, CLIMBING, OR FENCING; BALL GAMES; TRAINING EQUIPMENT
    • A63B2230/00Measuring physiological parameters of the user
    • A63B2230/40Measuring physiological parameters of the user respiratory characteristics
    • A63B2230/405Measuring physiological parameters of the user respiratory characteristics used as a control parameter for the apparatus
    • AHUMAN NECESSITIES
    • A63SPORTS; GAMES; AMUSEMENTS
    • A63BAPPARATUS FOR PHYSICAL TRAINING, GYMNASTICS, SWIMMING, CLIMBING, OR FENCING; BALL GAMES; TRAINING EQUIPMENT
    • A63B2230/00Measuring physiological parameters of the user
    • A63B2230/40Measuring physiological parameters of the user respiratory characteristics
    • A63B2230/43Composition of exhaled air
    • A63B2230/433Composition of exhaled air partial CO2 value
    • AHUMAN NECESSITIES
    • A63SPORTS; GAMES; AMUSEMENTS
    • A63BAPPARATUS FOR PHYSICAL TRAINING, GYMNASTICS, SWIMMING, CLIMBING, OR FENCING; BALL GAMES; TRAINING EQUIPMENT
    • A63B2230/00Measuring physiological parameters of the user
    • A63B2230/40Measuring physiological parameters of the user respiratory characteristics
    • A63B2230/43Composition of exhaled air
    • A63B2230/433Composition of exhaled air partial CO2 value
    • A63B2230/435Composition of exhaled air partial CO2 value used as a control parameter for the apparatus
    • AHUMAN NECESSITIES
    • A63SPORTS; GAMES; AMUSEMENTS
    • A63BAPPARATUS FOR PHYSICAL TRAINING, GYMNASTICS, SWIMMING, CLIMBING, OR FENCING; BALL GAMES; TRAINING EQUIPMENT
    • A63B2230/00Measuring physiological parameters of the user
    • A63B2230/50Measuring physiological parameters of the user temperature
    • AHUMAN NECESSITIES
    • A63SPORTS; GAMES; AMUSEMENTS
    • A63BAPPARATUS FOR PHYSICAL TRAINING, GYMNASTICS, SWIMMING, CLIMBING, OR FENCING; BALL GAMES; TRAINING EQUIPMENT
    • A63B71/00Games or sports accessories not covered in groups A63B1/00 - A63B69/00
    • A63B71/06Indicating or scoring devices for games or players, or for other sports activities
    • A63B71/0619Displays, user interfaces and indicating devices, specially adapted for sport equipment, e.g. display mounted on treadmills
    • A63B71/0622Visual, audio or audio-visual systems for entertaining, instructing or motivating the user
    • GPHYSICS
    • G01MEASURING; TESTING
    • G01FMEASURING VOLUME, VOLUME FLOW, MASS FLOW OR LIQUID LEVEL; METERING BY VOLUME
    • G01F1/00Measuring the volume flow or mass flow of fluid or fluent solid material wherein the fluid passes through a meter in a continuous flow
    • G01F1/68Measuring the volume flow or mass flow of fluid or fluent solid material wherein the fluid passes through a meter in a continuous flow by using thermal effects

Definitions

  • the invention relates to a device for training the respiratory function.
  • Respiratory training devices are used in particular to train the respiratory muscles, in particular for therapeutic purposes or to increase respiratory performance, for example for competitive sports.
  • a respiratory training device of this type is known from WO 02/081034. It has a branched air duct starting from a mouthpiece.
  • a first branch has a piston valve and is used to suck in fresh air or to discharge stale air.
  • a second branch is connected to a flexible air bag. When you exhale, the air bag is first filled with exhaled air. Only when this is full and a certain overpressure, which can be set on the piston valve, has been reached inside the device, the piston valve opens and more air flows outside via the first branch. Conversely, when inhaling, the air from the air bag is inhaled first, and only when there is a negative pressure in the device does the piston valve open, whereby ambient air is sucked in.
  • the first branch has two piston valves, one of which is used to control the amount of fresh air entering the air duct, and one is used to control the amount of stale air exiting the air duct.
  • the design of the breathing training device with an air bag serves to prevent the CCh concentration in the blood of the person exercising from decreasing too much during endurance training (hyperventilation).
  • Adaptation to the characteristics of the exercising person - in particular the capacity of the lungs of the exercising person - is determined by the choice of the size of the air bag.
  • US 2018/0120245 relates to a sensor for breathing air with which a CCL content of the air can be measured, among other things, by measuring thermal conductivities.
  • a breathing training device of the type taught in WO 02/081034, in which a first branch is open to the atmosphere and a second branch is provided with an air bag.
  • a processor module can adjust the concentration of the carbon dioxide content of the inhaled air by measurements on both branches in order to avoid hyperventilation.
  • Document EP 3 141 289 also shows a respiratory training device.
  • this has two channels following a mouthpiece, one of which can only be flown through by exhaled air and the other only by air that is inhaled, for which there are check valves.
  • the channel for the air to be inhaled is provided with a connection for a breathing air mixture, for example with special substances, and an outlet into a breathing air bag.
  • the channel for the air to be inhaled is provided with an outlet to the atmosphere and an inlet from the breathing air bag.
  • a plurality of sensors can be present in each of the channels, for example pressure sensors, gas composition sensors, flow sensors. This allows the flow mixtures of the inhaled and exhaled air to be regulated individually.
  • the devices presented in US 2018/0120245 and in EP 3 141 289 are potentially complex in terms of construction and control.
  • a respiratory training device which has an air guiding arrangement with a mouthpiece and a branched air duct adjoining the mouthpiece with a mouthpiece branch to which the mouthpiece is attached, a first branch and a second branch.
  • the first branch has an inlet / outlet opening and is used for the entry of fresh air and the discharge of used air.
  • the second branch has a flexible air container, for example a flexible air bag, which is used to store exhaled air so that the user can inhale it again.
  • the respiratory training device is characterized in that it has a first electrically controlled valve and a second electrically controlled valve, the first and the second valve being arranged so that the airway between the mouthpiece and the inlet / outlet opening and the air path between the mouthpiece and the air container can each be opened or closed independently of one another and a flow resistance can be set at least between the mouthpiece and the inlet / outlet opening.
  • At least one of the two valves is an adjustable valve.
  • both valves can be adjustable.
  • the term “adjustable valve” generally refers to a control element through which the volume flow of a fluid, that is to say a liquid or a gas, can be controlled.
  • the term “adjustable valve” is therefore to be understood in accordance with the English meaning “control valve” and does not mean a restriction to a specific design of the control element.
  • the adjustable valve can also be manufactured in one of the types that are sometimes referred to as “flap”, “slide”, “cock” or “valve in the narrower sense of the word” etc.
  • the divisibility can be continuous in the narrower sense of the word or approximately continuous by making available many levels.
  • An example of an approximately continuously adjustable valve is a valve with a flap or another control element that is moved between two extreme positions by a stepper motor.
  • Adjustable valves differ from “on / off” valves, which only allow a setting between two switching states, for example “open” and “closed”.
  • the mouthpiece branch means a part of the air ducting arrangement that is not branched in itself and forms a coherent volume that extends to the branch between the first and the second branch.
  • the mouthpiece branch is so designed and arranged that all exhaled air flows through the mouthpiece branch and from there into the first and / or second branch, and that all air to be inhaled coming from the first and / or second branch through the Mouthpiece branch goes.
  • all of the air to be inhaled and, in particular, all of the exhaled air necessarily passes through the volume which the sensors present in or on the mouthpiece are present.
  • the first and second valves are controlled by a control unit which, in addition to controlling the valves, can also have other functions and which in particular also reads out the sensors, etc.
  • the control unit is to be understood as a functional unit in this text. It can be a physical entity, for example a chip or a circuit board with several chips and / or other electronic components. However, it can also be designed to be physically distributed over different devices, for example by a sensor chip (or similar) partially assuming functions that are assigned to the control unit here.
  • first and second adjustable io valve are conceivable:
  • the first adjustable valve is in the first branch and the second adjustable valve (or possibly a second valve, which is not adjustable but an "on / off") Valve is) arranged in the second branch, ie Both valves are arranged on the far side of the branching of the air guide arrangement as seen from the mouthpiece.
  • Both adjustable valves 15 can then be controlled in a simple manner by increasing or decreasing the flow cross-section - up to a closed state with a flow cross-section 0.
  • a first adjustable valve is located in front of the branch in relation to the mouthpiece and can control a total st) flow cross section.
  • a second adjustable valve is then designed as a directional valve and, in a state in which it releases a connection between the first branch and the mouthpiece branch and blocks a connection between the second branch and the mouthpiece branch, a state in which it allows both connections, in a state in which it blocks a connection between the first branch and the mouthpiece branch 25 and releases a connection between the second branch and mouthpiece branch, as well as being brought into states lying in between.
  • the first adjustable valve is such a directional control valve and the second adjustable valve is a valve in one of the two branches that controls the flow cross section. Such an arrangement also ultimately allows the two airways mentioned to be opened or closed independently through the interaction of the two adjustable valves.
  • a pressure relief valve can be present, for example. This makes particular sense in the second branch, for example, because external pressure on the flexible container can greatly increase the pressure in the interior of the air duct arrangement in a desired or undesired manner.
  • a pressure relief valve protects the components used from damage.
  • the breathing training device can be operated in various operating modes by the valves that can be controlled by the control unit. This can be particularly advantageous in combination with a CCh sensor, a flow sensor and / or a pressure sensor.
  • the respiratory training device can be set up to operate them.
  • the breathing training device also has means to carry out this operation.
  • Such means include programming of the respiratory training device and specifically of its control unit, either permanently or in the form of a loadable software module.
  • the airway between the mouthpiece and flexible container can be at least partially open, while the airway between the mouthpiece and the inlet / outlet opening is partially closed (ie the flow resistance is high and / or this airway is completely closed at times).
  • the user is enabled to inhale and exhale at a high breathing rate without hypocapnia occurring, since in this mode of operation a large part of the exhaled air is inhaled again.
  • the proportion of this air and the fresh air can be controlled by setting at least the flow resistance on the air path between the mouthpiece and the inlet / outlet opening and, for example, in particular by individually setting the flow resistance through both branches. It is particularly favorable if a control loop is formed via the control unit in which the measured CCh content (for example expiratory, in particular end expiratory, see also the comments below) is used as the controlled variable.
  • the airway between the mouthpiece and the flexible container is closed, and the airway between the mouthpiece and the inlet / outlet opening is either completely closed until a certain pressure is reached (threshold value), or partially closed so that the Flow resistance is significant.
  • training and / or measurements can relate to both expiration and inspiration.
  • the flow resistances during expiration and inspiration can also be selected differently.
  • the control unit is therefore set up in particular to control the valves mentioned both during an inspiration phase and during an expiration phase. This can be done in particular on the basis of values measured only during the inspiration phase, especially on the basis of CO2 concentration determined only during the inspiration phase.
  • a special way of using the advantages of the procedure according to the invention with the at least one valve that can be controlled and adjusted by the control unit is to provide a vibration mode. It has been shown that vibration breathing training is particularly advantageous when releasing mucus in the airways.
  • vibration mode the adjustable valve or at least one of the adjustable valves or both adjustable valves are operated in a vibration mode in which the flow resistance is periodically changed in a vibration frequency, for example between a very high value (flow cross-section 0 or close to 0) and a moderate value. This enables an oscillating pressure amplitude during exhalation or inhalation with a corresponding vibration frequency, which brings the mentioned advantageous properties with it.
  • Frequencies below 50 Hz but above 5 Hz have proven to be favorable vibration frequencies; Frequencies around 20 Hz to 25 Hz are particularly favorable.
  • both valves are adjustable, in particular both valves can vibrate in the vibration training mode, preferably in unison.
  • a flow sensor is present, a total volume of the air exhaled during a single expiratory phase or also over several expiratory phases can be determined and a spirometric measurement can be carried out.
  • the procedure according to the invention with the at least one valve controllable and adjustable by the control unit also enables operating modes as required, for example the “interval training” operating mode with operating parameters changing at adjustable intervals, or user-defined operating modes.
  • the adjustable valve or at least one of the adjustable valves can be a flap valve; in particular, both valves (i.e. the first and the second controllable valve) can be flap valves.
  • Flap valves of the type described here have a flap which can be pivoted about an axis of rotation within the air guide arrangement and in this way can close the flow cross-section of airways or continuously / gradually increase or decrease it.
  • Flap valves have been found to be particularly favorable, the axis of rotation of which leads approximately through the center of gravity of the flap, which is thus arranged approximately in the middle of the flap. With these no inertial mass has to be shifted for actuation of the respective valve, so that they run particularly smoothly and are particularly suitable for very quick adjustments of the flow cross-section or for very quick opening / closing of the airway.
  • Such flap valves with an axis of rotation through the center of gravity are particularly suitable for arrangements in which they are each arranged in a tube section - with a round or non-circular cross section of the lumen in the tube, the tube cross section, for example, immediately in front of and immediately behind the flap, for example constant is.
  • flap valves are particularly suitable for embodiments which, among other things, provide operating modes in which the flow cross-sections change very quickly and / or very often, for example the vibration training mode mentioned.
  • flap valves with an axis of rotation due to the center of gravity are particularly suitable for designs in which the first valve is arranged in the first branch and the second valve is arranged in the second branch.
  • the flap valve is driven in particular electrically, via a suitable motor. Stepper motors have proven to be particularly suitable.
  • the respiratory training device has, for example, a CCk sensor.
  • a CCk sensor should in particular be set up and arranged accordingly to measure the CCk content of the exhaled and / or possibly the inhaled air. The measurement does not have to result in a numerical value for the percentage CCk content. It is sufficient if a measured value is determined which clearly correlates with the C0 2 content and which enables the adjustable valve (s ) to be regulated so that the C0 2 content can be regulated within a certain range.
  • measurements that produce a value that correlates with the C0 2 content also not necessarily a numerical value for the percentage of C0 2 in the air, are also referred to as measurements of the C0 2 content.
  • C0 2 sensors are known per se, and the present invention is suitable for the use of C0 2 sensors of various types. According to special embodiments, however, the invention makes use of a relationship existing for devices of the type according to the invention and proposes using the device with a CO 2 sensor of a particularly economical, newly developed type.
  • These embodiments are based firstly on the knowledge that the thermal conductivity of air saturated with moisture depends on the CCh concentration in this air. Second, it is based on the knowledge that the exhaled air (especially, but not only end-expiratory) has both a known humidity (of 100%) and a known temperature (body temperature). If all other parameters are kept constant, the heat dissipated from or supplied to a heated or cooled body will therefore depend on the CCL content of the air.
  • the heat dissipated by a heating wire will depend on this CCL content.
  • a measuring cell then contains a heating element, for example a heating wire. The heating element is heated during the measurement.
  • the required heating power in relation to the temperature reached in a steady state is a measure of the convection cooling to which the heating element is subjected when the exhaled air flows through it at a constant flow.
  • the temperature of the heating element can be measured directly or regulated to a specific desired value, or also indirectly, for example by the electrical resistance being a measure of the cooling.
  • the result of the measurement can be used as a measure of the C0 2 content.
  • the power can be kept constant and the electrical resistance (measure for the temperature) used as a measured variable, or conversely, the current flow through the heating element can be regulated so that after a short start ramp the electrical resistance as a measure for the temperature is constant is maintained and the required power (measure for the heat transfer) is used as a measured variable.
  • this method of measuring the CC content requires that the flow of the diverted air portion is constant - otherwise the required power also depends - critically - on the flow through the measuring cell. This is achieved by firstly keeping a flow opening through which the air enters the side branch with the measuring cell so that pressure fluctuations in the relevant branch (e.g. mouthpiece branch) of the air duct arrangement are not reflected in flow changes. On the other hand, this can be done by additionally conveying the air through the side branch by a pump, the pump having a constant pumping capacity.
  • Such a pump runs, for example, constantly or only during a measurement phase.
  • a measurement phase is selected in particular so that the CCh content is measured in each case in the end expiratory phase.
  • This point in time can be determined by the control unit, in particular using the results of the flow measurement, which will be explained below.
  • the flow measurement firstly allows a clear differentiation between the inspiration and expiration phase and secondly it enables the determination of the point in time at which the expired air flow decreases at the end of the expiration phase.
  • the C0 2 sensor can in particular be arranged in the mouthpiece branch (or mouthpiece); an arrangement on the mouthpiece branch or mouthpiece, for example via a branched-off side branch with constant flow that functions as mentioned, is also meant.
  • the arrangement of the CC sensor in the mouthpiece branch / mouthpiece as the only CC sensor enables a particularly efficient and simple structure. It has been shown in particular that a single CC sensor in the mouthpiece is sufficient to regulate the device in such a way that hypocapnia can be prevented.
  • the CCh concentration of the inhaled air in the mouthpiece branch is not easy to determine because neither the humidity nor the temperature are known, as the mixing ratio is also not known.
  • the prior art therefore suggests measuring the C0 2 concentration where it is known exactly where the air is coming from, and then adjusting the mixing ratio to a desired value.
  • embodiments of the present invention are based on the knowledge that, firstly, the C0 2 concentration of the exhaled air in the mouthpiece branch can be better determined in contrast to the inhaled air and, secondly, that this is suitable as a control variable, even if the concentration is ultimately in the inhaled air determines what the user breathes.
  • the CCL concentration of the exhaled air is meaningful in this regard.
  • the arrangement in the mouthpiece branch is based on the above-mentioned approach of taking the measurements expiratory, for which the device can be appropriately equipped and programmed. This is in contrast, for example, to the approach according to US 2018/0120245.
  • the controlled variable is then the C0 2 content of the exhaled air or another variable that is dependent on it and also takes other values into account. It has been shown that this indirect procedure using the exhaled air is just as suitable as a regulation directly from the CC content of the air to be inhaled, which requires more complex sensors.
  • the device preferably also has a flow sensor.
  • a flow sensor can be based on any of the many known measuring principles for measuring the gas flow.
  • the flow sensor corresponds to a principle similar to the aforementioned C0 2 sensor (whereby the measuring principles of the flow sensor and the C0 2 sensor can be selected independently of one another, that is, for example, both sensors do not have to be based on this measuring principle, but that can also be the case for only one or the other of the two or for none at all.
  • the flow sensor has a heating element, for example a heating wire, which is heated with a known, predetermined or measured power.
  • a heating element for example a heating wire
  • the heating power required to maintain a known (directly or indirectly measured or controlled) temperature depends primarily on the flow, provided the flow is laminar.
  • An additional dependence on the CO2 concentration, which can be used in the possible CCL sensor, can be viewed as negligible according to a first option, since changes in the heating power caused by flow changes in relation to the temperature are much more significant than those caused by changes in the C0 2 concentration in the area of interest.
  • this dependency can be compensated arithmetically, in embodiments in which a value characteristic of the C0 2 concentration is known from the C0 2 measurement.
  • the device has, for example, a laminarization device connected upstream of it, which laminarizes the air flow as it flows through the flow sensor by preventing any vortex formation.
  • laminarization devices can, in particular, have structures made up of many parallel tubular elements, for example in the form of a honeycomb.
  • the device according to the invention has, for example, a pressure sensor in embodiments.
  • a pressure sensor in embodiments.
  • Such a device can be designed in a manner known per se and, for example, be arranged in the mouthpiece branch or in a (further) side branch branched off from it.
  • control unit can in particular also have or enable a user interface.
  • a user interface For this purpose it has, for example, an interface via which you can communicate with an external device - typically a computer (server, desktop, laptop, tablet, smartphone, etc.) - and / or with a dedicated user interface, for example a screen for the Display of user feedback, can communicate.
  • an external device typically a computer (server, desktop, laptop, tablet, smartphone, etc.)
  • a dedicated user interface for example a screen for the Display of user feedback
  • FIG. 1 shows a view of a device according to the invention
  • 2 shows a schematic cross-sectional illustration of a
  • Device 3 and 4 show the device according to FIG. 2 in different states during the expiratory phase and during the inspiration phase;
  • Fig. 5 is a block diagram of a device; 6-8 schematically each an alternative device; 9 schematically shows a detail of a C0 2 sensor; 10 shows a detail of a pressure sensor; and FIG. 11 shows a feedback display for force measurements.
  • FIG. 1 shows a respiratory training device 1 of the type according to the invention in a view.
  • An air duct assembly 10 is a system of branched pipes.
  • the tubes form a mouthpiece branch 11, which starts from a mouthpiece 21, a first branch 12 and a second branch 13.
  • the second branch opens into a flexible air reservoir 31.
  • elements of a control system which are described in greater detail below, and possibly also elements of the sensor system also described below are arranged.
  • the first branch 12 forms an inlet / outlet opening 45 which can also be provided with a filter (not shown in the figures) or similar.
  • a filter not shown in the figures
  • the adjustable valves are designed as flap valves, ie they each have a flap 48 which is rotated around an axis of rotation 49 between a corresponding branch releasing state and a locking state is pivotable. It is also possible to adopt states between these two extremes, so that the cross section available for the air flow can be set, which enables the volume flow to be set (with a given pressure difference).
  • the flap valves are designed such that the axis of rotation lies on the center of gravity of the flaps, which brings the advantages explained above with it.
  • FIG. 2 shows a configuration in which the first flap valve opens only slightly and thus only allows a small flow, while the second flap valve 42 is fully open. Shown is the configuration while the user is exhaling, whereby the exhaled air for the most part flows into the flexible container 31 and a small part flows out of the device through the inlet / outlet opening 45.
  • Figure 4 shows a configuration in which both adjustable valves 41, 42 are partially open during the process of inhalation by the user. The two partially open flap valves ensure a certain ratio between used and fresh inhaled air, which can be adjusted by the position of the flaps, whereby, as described in more detail below, the C0 2 content in the air can be regulated using a suitable sensor.
  • a CCk sensor 51, a pressure sensor 52 and a flow sensor 53 are also shown schematically in FIG.
  • a lamination arrangement 57 in the mouthpiece can, for example, have an arrangement of walls running parallel to the flow direction, which have a honeycomb structure form, ie form a pattern of hexagonal cells in a section perpendicular to the direction of flow (ie also perpendicular to the plane of the drawing in FIG. 2).
  • the laminarization device - which can also have a physical structure other than a honeycomb structure - laminarizes the flow of the exhaled air, which, as described in this text, contributes to the measurability of the gas flow.
  • An optional bacteria filter 56 is also visible in FIG. 2.
  • the sensors mentioned are connected to a control unit of the device and they are read out via this. This can be done by feeding the sensor signal into the control unit with or without prior A / D conversion and evaluating it there. This includes the possibility that electronic components are assigned to the sensors, which steps carry out this evaluation themselves and which are therefore assigned to the control unit 60 in terms of their function.
  • FIG. 5 shows a schematic structure of the control and regulation components.
  • the control unit 60 is to be understood as a functional unit. It can be a physical entity, for example a chip or a circuit board with several chips and / or other electronic components. However, it can also be designed to be physically distributed over different devices, for example by a sensor chip (or similar) forming part of the control unit by producing a control signal directly, for example.
  • the control unit controls stepper motors 47, by means of which the flaps 48 of the flap valves 41, 42 are moved.
  • the control unit has an interface 61 for communication with an external device, for example a computer 63 (desktop, laptop, tablet, smartphone, etc.) with appropriate software, a dedicated operating console or a user interface.
  • there is also a user display 64 which, for example, via the computer (or the operating console) or also directly from the control unit coming from, a feedback for the user of the breathing training device can be presented.
  • the adjustable valves (flap valves 41, 42 in the example shown) are set during exhalation in such a way that a large part of the exhaled air (initially all of the exhaled air) is collected in the flexible container 31. If the flexible container 31 is filled - also depending on the container size - an overpressure and underpressure valve 71, which is attached between the flexible container 31 and the valve 41 of the corresponding arm, opens, and the further exhaled air flows out, as in FIG. 3 shown. When inhaling, conversely, due to the setting of the adjustable valves, the air present in the container is at least for the most part inhaled again, supplemented by fresh air from the inlet / outlet opening 45 (FIG. 4).
  • the adjustable valves are set in such a way that the measured end-expiratory CCh concentration is set to a value that is, for example, in the normocapnic range (4.5-6% CO2 end-expiratory). If the air in the flexible bag is insufficient for inhalation, the overpressure and underpressure valve 71 opens so as not to change the flow resistance.
  • the device thus forms a control loop in which the controlled variable is the CCL concentration, the setting of the first adjustable valve (first flap valve 41 in the example shown) or the settings of both adjustable valves that form the manipulated variable (s).
  • the second valve 42 can also be constantly open in the “endurance training” operating mode and therefore does not have to be an adjustable valve.
  • the second valve is also an adjustable valve, which makes it easier to adjust the proportions of used and fresh air during an entire breath is made possible.
  • feedback displayed in real time via the user display 64 can moreover be particularly valuable in order to regulate the breathing depth, breathing rate and the duration of the training.
  • overpressure valve and the underpressure valve are implemented in the described embodiment in a single element, the overpressure and underpressure valve 71 mentioned. But they can also be implemented by an independent pressure relief or vacuum valve.
  • Strength training In the "strength training" operating mode, the second adjustable valve (second flap valve 42) is closed.
  • the first adjustable valve is set, for example, in such a way that it offers a certain, relatively large flow resistance at least during exhalation.
  • the first adjustable valve can in particular also be operated in such a way that it closes completely during strength training and only opens a little when the measured pressure exceeds a threshold value (threshold value training).
  • feedback displayed in real time via user display 64 can also be particularly valuable.
  • the pressure reached can be displayed in relation to the threshold pressure to be achieved via a suitable bar symbol with a bar that grows or shrinks according to the pressure, so that the user can see when he is getting close to the threshold pressure to be reached.
  • the flow resistance is high, the pressure to be achieved and the current pressure can be displayed.
  • Spirometry In the "Spirometry" operating mode, at least the first adjustable valve is open. The second adjustable valve can be closed. The flow of the Exhaled air is recorded by the flow sensor and the volume of exhaled air is determined through integration.
  • Maximum respiratory muscle strength In this operating mode, the maximum inspiratory and expiratory strength can be measured. Both adjustable valves are completely closed. Through explosive exhalation or inhalation with completely full or empty lungs, the maximum strength of the respiratory muscles can be measured by the pressure sensor.
  • Vibration Based on the "Endurance training" operating mode and / or the "Strength training” operating mode and / or the “Interval training” operating mode (see below), at least one of the adjustable valves, for example both adjustable valves (for endurance vibration training), is operated to vibrate.
  • the vibration frequency can be between 5 Hz and 50 Hz, for example between 15 Hz and 35 Hz, in particular between approx. 20 Hz and approx. 30 Hz. It has been shown that vibration breathing training is particularly beneficial when releasing mucus from the airways.
  • the approach according to the invention with the two valves enables vibration training by the same device, which can also be used for endurance training and also protection against hyperventilation (via the CCL measurement and a corresponding control), the ability to set various parameters (respiratory volume resistance, etc. .) and the feedback function also apply to the "Vibration" operating mode.
  • Interval training In particular in combination with feedback via the user display 64, interval training can also be provided.
  • a specification (a level displayed via the user display, for example in relation to the current performance and / or force) and / or the resistances imposed on the user (by Settings of the adjustable valves) change at specified intervals.
  • CC regulation takes place in the same way as the 'endurance training' operating mode.
  • Step test In the 'step test' operating mode, the endurance strength of the respiratory muscles is tested.
  • the breathing depth and the breathing rate are regulated via the user display 64.
  • the flow resistance is regulated using the two valves so that, in combination with the respiratory volume and the respiratory frequency, the work of breathing can be gradually increased until the respiratory muscles tire (analogous to a bicycle step test of the known type).
  • a typical protocol could be as follows: The breathing depth is a constant 60% of the vital capacity measured previously (see operating mode, spirometry 4 ), and the breathing frequency is increased by two breaths per minute every two minutes, starting with 16 breaths per minute.
  • the breathing resistance By setting the breathing resistance with the two valves 41, 42 and, for example, also setting the breathing rate, the work of breathing is increased by 10% every two minutes until the breathing muscles get tired.
  • other step test protocols can also be implemented.
  • the CCh regulation takes place as in the operating mode, endurance training.
  • Customized Training Any profiles and sequences of training and / or measuring steps useful for the current user can be programmed via the interface.
  • FIGS. 2-4 has a particularly favorable arrangement of the at least two adjustable valves.
  • Other arrangements are shown schematically in Figures 6-8.
  • Fig. 6 shows an arrangement that is easy to handle in the control, like the embodiment of Figs. 2-4, with the first adjustable valve 41 in the mouthpiece branch 11.
  • This first adjustable valve makes the overall Flow cross-section controllable, ie the first adjustable valve alone sets the resistance (inspiratory and expiratory) against which the user has to breathe.
  • the first valve 41 can also close completely, particularly in the “strength training” operating mode. In the "Vibration" operating mode, it may be sufficient if only the first valve vibrates.
  • the second adjustable valve 42 is designed as an adjustable directional valve and can switch between a state in which it releases a connection between the first branch and mouthpiece branch and blocks a connection between the second branch and mouthpiece branch, and a state in which there is a connection between first branch and mouthpiece branch blocks and a connection between the second branch and mouthpiece branch releases, movable. Conditions in between enable one
  • Fig. 6 the second adjustable valve is illustrated schematically as a pivotable flap.
  • both the flow cross-section between the mouthpiece and the air container and the flow cross-section between the mouthpiece and the inlet / outlet opening can each be set between 0 and a maximum value and can be selected independently of one another.
  • a C0 2 regulation as described above with reference to the operating mode, endurance training is also possible in this way.
  • the CC sensor 51 can be based on a principle known for CCh sensors.
  • CCh sensors are known which function as infrared sensors and use the known fact that CO2 is an efficient IR absorber.
  • CO2 is an efficient IR absorber.
  • Such sensors are reliable and can be placed directly in the respiratory flow however, the disadvantage that they are relatively complex to manufacture and operate and correspondingly expensive.
  • the CCh sensor 51 can also be based on the new, alternative functional principle mentioned, according to which a portion of the exhaled air is branched off with a constant flow.
  • a measuring cell 83 then contains a heating element, for example a heating wire. The heating element is heated during the measurement.
  • the required heating power in relation to the temperature reached in a steady state is, as explained above, a measure for the convection cooling and thus, given constant other parameters, a measure for the CCL content.
  • FIG. 9 schematically illustrates the principle of such a possible CCh sensor.
  • a CC sensor side branch 82 branched off particularly from the mouthpiece branch or 11, possibly directly from the mouthpiece, air is sucked in via a connection opening 81 with a small cross section during expiration, in particular at the end of the expiratory phase, for example by a small pump 84 constant delivery rate.
  • the side branch for example, also has a small cross section of, for example, between 0.7 mm and 1.5 mm.
  • the branched off air reaches the measuring cell 83 before or after passing through the pump 84, where measurement is carried out according to the principle explained above.
  • the control unit will, for example, use the flow measurement to determine the time of the CCh measurement.
  • control unit can initiate the CCh measurement towards the end of the expiratory phase, when the flow caused by expiration through the mouthpiece branch decreases again.
  • the pump 84 can deliver constantly or at the mentioned times of the CO2 measurement; the same applies to the heating of the heating element.
  • the pressure measurement - with, for example, a conventional pressure sensor element 92 - can optionally take place on a branch 91 branched off from the mouthpiece branch 11 or possibly from the mouthpiece, as shown in FIG.
  • the flow measurement can be done with any suitable flow sensor.
  • flow sensors of various types on the market for this purpose and the present invention does not exclude any of the various measuring principles.
  • the flow sensor 53 in the embodiment illustrated here is based on the following measuring principle, which is analogous to the CC sensor described above:
  • a heating element for example a heating wire, is heated with a known heating power.
  • the heating power required to maintain a certain temperature is a measure of the heat dissipated by the flow air, which in turn is a measure of the flow at constant (defined) air temperature and humidity and with laminar flow.
  • the amount of heat dissipated per unit of time also depends on the CCL content. However, if the CCL content is kept approximately constant by the control, this influence is small compared to the influence of the flow, i.e. a possible measurement error would not be great. Second, if a particularly precise measurement is required, it can also be corrected mathematically, since the CCL content is known from the CCL measurement carried out in parallel.
  • the measurement of the flow through the flow sensor is carried out by the control unit during expiration.
  • Exhaled air has a known temperature and humidity.
  • the air flow of the exhaled is laminar due to the laminarization device.
  • the flow can be corrected mathematically based on the measured pressure. Therefore, the measurement described above gives meaningful measured values.
  • a value for the flow can be determined from the measurement and a value for the exhaled volume can be determined through integration over time.
  • the relationship between temperature (or electrical resistance) on the one hand and heating power in the steady state on the other hand can be used for this purpose.
  • FIG. 11 illustrates another optional feature of the feedback display for the user via the user display 64, which is also optionally available.
  • a threshold value display 101 is activated. This shows the current pressure reached by the user in relation to a threshold 103 to be reached via a display element, for example a bar 102 or similar, and thus gives the user an immediate impression of the goal still to be reached.
  • Other feedback displays are of course also possible.

Landscapes

  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Pulmonology (AREA)
  • Veterinary Medicine (AREA)
  • Engineering & Computer Science (AREA)
  • Biomedical Technology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Animal Behavior & Ethology (AREA)
  • Public Health (AREA)
  • Emergency Medicine (AREA)
  • Anesthesiology (AREA)
  • Hematology (AREA)
  • Physical Education & Sports Medicine (AREA)
  • Biophysics (AREA)
  • Orthopedic Medicine & Surgery (AREA)
  • Physiology (AREA)
  • Physics & Mathematics (AREA)
  • Pathology (AREA)
  • Medical Informatics (AREA)
  • Molecular Biology (AREA)
  • Surgery (AREA)
  • Obesity (AREA)
  • Measurement Of The Respiration, Hearing Ability, Form, And Blood Characteristics Of Living Organisms (AREA)

Abstract

L'invention concerne selon un aspect un appareil d'exercice respiratoire, qui renferme un ensemble de guidage d'air pourvu d'un embout (21) et d'un canal d'air raccordé à l'embout, formant un embranchement. Ce dernier forme une branche (11) d'embout, sur laquelle l'embout est installé, une première branche (12) et une deuxième branche (13). La première branche (12) comporte une ouverture d'entrée/de sortie (45) et sert à l'entrée d'air frais et à la distribution d'air vicié. La deuxième branche (13) comporte un contenant d'air (31) flexible, par exemple un sachet d'air flexible, lequel sert au stockage d'air expiré aux fins d'une nouvelle inspiration de celui-ci par l'utilisateur. L'appareil comporte une première soupape (41) à pilotage électrique et une seconde soupape (42) à pilotage électrique. La première et la seconde soupape sont disposées de telle sorte que la voie entre l'embout (21) et l'ouverture d'entrée/de sortie (45) et la voie entre l'embout (21) et le contenant d'air (31) peuvent être ouvertes ou fermées respectivement indépendamment l'une de l'autre, et une résistance à l'écoulement au moins entre l'embout (21) et l'ouverture d'entrée/de sortie (45) peut être réglée.
EP20723374.3A 2019-05-02 2020-04-30 Appareil d'exercice respiratoire Pending EP3962612A1 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
CH00587/19A CH716144A1 (de) 2019-05-02 2019-05-02 Atemtrainingsgerät.
PCT/EP2020/062058 WO2020221872A1 (fr) 2019-05-02 2020-04-30 Appareil d'exercice respiratoire

Publications (1)

Publication Number Publication Date
EP3962612A1 true EP3962612A1 (fr) 2022-03-09

Family

ID=66589144

Family Applications (1)

Application Number Title Priority Date Filing Date
EP20723374.3A Pending EP3962612A1 (fr) 2019-05-02 2020-04-30 Appareil d'exercice respiratoire

Country Status (3)

Country Link
EP (1) EP3962612A1 (fr)
CH (1) CH716144A1 (fr)
WO (1) WO2020221872A1 (fr)

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE102021002014A1 (de) 2021-04-19 2022-10-20 Guido Kohler Atemtrainingsgerät und Verfahren zur Durchführung eines Atemtrainings
CN114392533A (zh) * 2022-01-09 2022-04-26 朱国彪 一种提高肺等呼吸系统功能的方法及饮水杯
CN115155013B (zh) * 2022-07-05 2023-05-16 宁波大学医学院附属医院 一种慢阻肺患者便携式肺功能康复训练装置
CN116392777B (zh) * 2023-04-25 2024-08-13 卫宁健康科技集团股份有限公司 一种肺功能训练装置及训练数据处理方法

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1254288C (zh) * 2001-04-10 2006-05-03 埃迪亚格公司 呼吸功能的训练机及其使用时对新鲜空气供入的监控方法
UA107438C2 (xx) * 2014-05-06 2014-12-25 Mykola Hryhorovych Liapko Тренажер дихальний (варіанти)
US10852261B2 (en) * 2016-10-29 2020-12-01 Sendsor Gmbh Sensor and method for measuring respiratory gas properties
CN109646783A (zh) * 2018-12-18 2019-04-19 湖南明康中锦医疗科技发展有限公司 呼吸阀、具有呼吸肌锻炼模式的呼吸支持设备及控制方法

Also Published As

Publication number Publication date
WO2020221872A1 (fr) 2020-11-05
CH716144A1 (de) 2020-11-13

Similar Documents

Publication Publication Date Title
EP3962612A1 (fr) Appareil d'exercice respiratoire
DE60212703T2 (de) Gasidentifikationssystem und volumetrisch korrigiertes gasabgabesystem
DE3636669C2 (de) Anordnung zur Zufuhr von Aerosol zu den Luftwegen und/oder Lungen eines Patienten
DE69811803T2 (de) Beatmungstubus
DE69936170T2 (de) Beatmungsgerät
EP1960025B1 (fr) Systeme de conduits flexibles pour appareils respiratoires
EP1377347B1 (fr) Appareil d'entraînement de la fonction respiratoire et procédé de commande d'admission d'air frais
DE19958532C1 (de) Beatmungsgerät mit einem Atemkreis
DE2314356A1 (de) Beatmungsgeraet
DE60116828T2 (de) Atembeutel für manuelle Beatmung
EP2563443A1 (fr) Procédé et dispositif pour administrer au moins un gaz médical à un patient sous assistance respiratoire au moyen d'un appareil d'assistance respiratoire
DE69911706T2 (de) Vorrichtung zur Unterstützung der Atmungsfunktion
DE112014007299T5 (de) Verfahren und Vorrichtung zur Messung von Atemweg-Widerstand und Lungennachgiebigkeit
EP2953692A1 (fr) Dispositif et procédé permettant de mettre en oeuvre un entraînement respiratoire
DE2910094A1 (de) Automatisches beatmungsgeraet mit leistungskontrolle, insbesondere fuer wiederbelebungs- und anaesthesie-zwecke
DE60317309T2 (de) Beatmungsvorrichtung
DE202023106692U1 (de) Dynamisch adaptiver Atemwegsstabilisator
DE4023108C1 (fr)
EP3261698B1 (fr) Dispositif respiratoire
EP4141846A1 (fr) Système de simulation de la respiration d'un organisme vivant
DE102010035167A1 (de) Respirator
DE2424025B1 (de) Beatmungsgerät
EP2704680B1 (fr) Procédé de commande d'un appareil d'entraînement
DE102021113642A1 (de) Verbindungs-Anordnung mit einem Volumenfluss-Sensor und einer Homogenisierungseinheit zur künstlichen Beatmung eines Patienten sowie ein Herstellungsverfahren
WO2022053094A1 (fr) Procédé et dispositif de mesure de la teneur en au moins un gaz dans l'air expiré

Legal Events

Date Code Title Description
STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: UNKNOWN

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: THE INTERNATIONAL PUBLICATION HAS BEEN MADE

PUAI Public reference made under article 153(3) epc to a published international application that has entered the european phase

Free format text: ORIGINAL CODE: 0009012

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: REQUEST FOR EXAMINATION WAS MADE

17P Request for examination filed

Effective date: 20211026

AK Designated contracting states

Kind code of ref document: A1

Designated state(s): AL AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HR HU IE IS IT LI LT LU LV MC MK MT NL NO PL PT RO RS SE SI SK SM TR

DAV Request for validation of the european patent (deleted)
DAX Request for extension of the european patent (deleted)
STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: EXAMINATION IS IN PROGRESS

17Q First examination report despatched

Effective date: 20240201

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: THE APPLICATION IS DEEMED TO BE WITHDRAWN