Device and method for artificial respiration in emergencies
10188813 ยท 2019-01-29
Assignee
Inventors
Cpc classification
A61M16/0003
HUMAN NECESSITIES
International classification
A61M16/00
HUMAN NECESSITIES
Abstract
A device and a method for artificial respiration in emergencies are proposed. The device comprises respiratory mask (40) which can be placed onto the nose and mouth section of a person to be provided with artificial respiration, a mouth section mouthpiece (41), through which respiratory air from an aider can be supplied, a flow tube (2) disposed between the respiratory mask (40) and the mouthpiece (41), which flow tube forms a continuous flow channel for the supplied respiratory air from the mouthpiece (41) to the respiratory mask (40), at least one sensor (10) disposed in the flow channel of the flow tube (2), which sensor measures parameters of the gases flowing through the flow channel, a processor disposed on the flow tube (2) and an output device (124). Here, the processor processes the mass or volumetric flow registered by the flow sensor (19) to form an output signal. The output device (124) emits the output signal.
Claims
1. A device for artificial respiration of a person in a medical emergency situation, comprising a respiratory mask which can be placed on the nose and mouth section of the person, a mouthpiece, through which respiratory air can be supplied by an aider, a flow tube disposed between the respiratory mask and the mouthpiece, which flow tube forms a continuous flow channel from the mouthpiece to the respiratory mask, at least one flow sensor disposed in the flow channel of the flow tube, wherein the at least one flow sensor can determine a mass or volumetric flow of a gas flowing through the flow channel, a processor designed to generate a characteristic penetration depth signal from the mass or volumetric flow registered by the at least one flow sensor for air flowing out of the nose and/or mouth of the person and through the flow channel during a cardiac massage as a result of a compression of the person's thorax down to a penetration depth, an output device configured to emit the characteristic penetration depth signal, and a push-on part configured to be connected detachably to the flow tube such that the push-on part encompasses the flow tube at least in part when connected to the flow tube, the processor and the output device being arranged in the push-on part; wherein the push-on part is configured to be selectively attached to the flow tube and configured to be selectively fastened to an arm of the aider during cardiac massage; and wherein the mass or volumetric flow is determined when the push-on part is selectively attached to the flow tube.
2. The device according to claim 1, further comprising a first vital signs sensor configured to register a proportion of oxygen and carbon dioxide in the air flowing through the flow channel, and wherein the processor is designed to process the registered proportion of oxygen and carbon dioxide into a vital signs output signal, which is emitted by the output device.
3. The device according to claim 2, further comprising a second vital signs sensor that registers a pressure difference in the flow channel as a vital sign of the person.
4. The device according to claim 1, wherein the output device comprises an optical display device.
5. The device according to claim 4, wherein the optical display device comprises an optically active surface on which the output signal is displayed, and wherein the optically active surface is a convex surface or essentially a flat surface, and wherein the flat optically active surface includes an angle of more than 0 and less than 90 with a longitudinal direction of the flow tube, where the longitudinal direction essentially corresponds to a direction of flow of the gas flowing through the flow channel.
6. The device according to claim 4, wherein the optical display device comprises several light-emitting diodes (LEDs).
7. The device according to claim 1, wherein the output device has an acoustic output device.
8. The device according to claim 1, further comprising an interface, wherein a mass or volumetric flow value registered by the at least one flow sensor or data derived therefrom can be emitted over the interface to an external device for emergency care, to a medical device, to a computer and/or to a mobile telecommunications device.
9. The device according to claim 1, wherein a filter is arranged in the flow channel between the mouthpiece and the at least one flow sensor and/or a filter is arranged in the flow channel between the respiratory mask and the at least one flow sensor.
10. The device according to claim 1, wherein the output device is designed to indicate whether the mass or volumetric flow registered or the characteristic penetration depth signal derived from the mass or volumetric flow or another parameter derived from the mass or volumetric flow lies within a specified range for resuscitation.
11. The device according to claim 1, wherein the push-on part comprises an arm fastening device configured to fasten the device to the arm of the aider, and wherein the push-on part comprises an acceleration sensor-configured to register an acceleration of the arm during a cardiac massage when the push-on part is fastened to the arm of the aider.
12. The device according to claim 11, wherein the processor is designed to generate an acceleration output signal from the acceleration registered by the acceleration signal, which acceleration output signal can be emitted by the output device.
13. A method for artificial respiration of a person in a medical emergency situation, using a device comprising a respiratory mask, a mouthpiece, a flow tube connecting the mouthpiece with the respiratory mask, a flow sensor arranged on the flow tube, a processor, an output device, and a push-on part connected detachably to the flow tube such that the push-on part encompasses the flow tube at least in part, the processor and the output device being arranged in the push-on part, wherein the push-on part is configured to be selectively attached to the flow tube and configured to be selectively fastened to an arm of an aider during cardiac massage; the method comprising process steps of: fitting the respiratory mask onto the nose and mouth section of the person, starting a cardiac massage of the person via compressing a thorax of the person down to a penetration depth and then allowing the thorax to decompress, registering, via the flow sensor, a mass or volumetric flow of a gas flowing out of the nose and/or mouth and flowing through the flow tube as a result of the cardiac massage while the push-on part is selectively attached to the flow tube, processing, via the processor, the mass or volumetric flow registered by the flow sensor to obtain a characteristic penetration depth signal for the penetration depth, and emitting, via the output device, the characteristic penetration depth signal.
14. The method according to claim 13, further comprising: registering, via an additional sensor, a proportion of oxygen and carbon dioxide in the gas flowing through the flow tube, processing, via the processor, the proportion of oxygen and carbon dioxide registered into a vital signs output signal, and emitting, via the output device, the vital signs output signal.
15. The method according to claim 13, further comprising: indicating, via the output device, whether the mass or volumetric flow registered or the characteristic penetration depth signal derived from the mass or volumetric flow or another parameter derived from the mass or volumetric flow lies within a specified range for resuscitation.
16. The method according to claim 13, further comprising: registering, via the flow sensor, an initial mass or volumetric flow of air flowing out of the nose and/or mouth of the person before the cardiac massage starts, and emitting, via the output device, whether the initial mass or volumetric flow registered is within a specified range for spontaneous breathing.
17. The method according to claim 13, further comprising: detaching the push-on part from the flow tube such that the push-on part no longer surrounds the flow tube, fastening the push-on part to the arm of the aider, registering, via an acceleration sensor of the push-on part, an acceleration with which the thorax is compressed during the compression of the thorax when the push-on part is fastened to the arm of the aider, determining a further characteristic penetration depth signal for the penetration depth from the acceleration determined, emitting, via the output device, the further characteristic penetration depth signal, and indicating, via the output device, whether the acceleration registered or the further characteristic penetration depth signal derived from the acceleration or another parameter derived from the acceleration lies within a specified range for resuscitation.
18. The method according to claim 17, wherein the push-on part is fastened to the wrist of the aider.
Description
DRAWING
(1) Model embodiments of the invention are represented in the drawing. Illustrations:
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DESCRIPTION OF THE MODEL EMBODIMENTS
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(19) The sensor section 9 is limited by four side walls 15, 16, 17, 18. The two side walls 15 and 17 are flat and run at an angle of 5 to each other. The angle can also lie between 2 and 20. The side wall 16 is likewise flat. It is adjacent to the two side walls 15 and 17. The fourth side wall 18 can likewise be flat or convex. If the fourth side wall 18 is flat in design, it is preferably parallel to the side wall 16. The four side walls 15, 16, 17, 18 produce the form of a truncated pyramid. The cross-section of the sensor section 9 is thus smaller at the end facing the cylindrical end section 5 of the flow tube 2 than at the end facing the cylindrical end section 6 of the flow tube 2. This is especially discernible in
(20) A first filter 19 and a second filter 20 are discernible in
(21) The push-on part 3 exhibits a housing 23. The housing 23 has a U-shape. It encompasses the sensor section 9 of the flow tube 2 from three sides so that the flat side walls 15, 16 and 17 are entirely covered by the push-on part. To that end, the push-on part exhibits three corresponding, flat side walls 24, 25 and 26 that rest on the side walls 15, 16 and 17. This is discernible in
(22) In the housing 23 of the push-on part 3 there are circuit boards 27 and 28 on which electrical and electronic components are arranged. These are in particular a memory device and a processor. In addition an analog-to-digital converter and a DC voltage source can be arranged on the circuit boards. A connector socket not discernible in the drawing and into which the upper end of the circuit board 11 of the sensor 10 is inserted is arranged on the side wall 25. The connector socket is connected to the circuit boards 27, 28. It forms the interface to the sensor 10. In addition a connector socket 29 that forms an interface with an external readernot represented in the drawingis arranged on the front side of the housing 23. A display device can in addition be integrated into a cover 30 of the housing 23.
(23) The two outer housing sections 31 and 32 cover the circuit boards 27, 28. They in addition exhibit handle elements 33, 34 that protrude outwards. These are equipped with grip recesses 35, 36 on their underside. The handle elements 33, 34 and the handle recesses 35, 36 facilitate pushing the push-on part 3 onto the flow tube 2 and lifting push-on part 3 off the flow tube 2.
(24) To provide artificial respiration for a person in an emergency situation, the respiratory mask 40 is fitted over the nose and mouth of the person in an emergency situation and secured to the head of the person in an emergency situation with the straps 43, 44. The sensor is either already activated or is specifically activated. It determines the gases flowing through the flow tube 2. These gases are analyzed by the processor to obtain measured values. The processor matches the measured values up with a corresponding instruction that is stored in the storage device. This is displayed on the display device and emitted to the aider. The determination of the parameters for the gases flowing in the flow tube also continues during first aid. As a result, the instructions given to the aider during the course of first aid can be adapted continually to any changes in the condition of the person in an emergency situation.
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(26) The surface of the push-on part 103 facing the viewer in
(27) The push-on part 103 exhibits two handle elements 127 at the side on the housing 123. The push-on part 103 can be removed from the flow tube 2 with the help of these handle elements.
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(30) The push-on part 103 is represented in the
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(32) To measure the mass or volumetric flow of a person, the device 103 with the respiratory mask 40 is placed onto the mouth and nose of the person. Using the input device 125, it is selected which group of people the person belongs to. The flow sensor in the flow tube determines the mass or volumetric flow of the air flowing out of the person. The mass or volumetric flow registered is displayed with the output device 124. If the mass or volumetric flow is too low, the aider administers a cardiac massage. If necessary the aider supplies air via the mouthpiece 41. In the cardiac massage, the mass or volumetric flow of the air flowing out of the person is determined. If no mass or volumetric flow is identified even though the penetration depth is increased, this is a sign of obstructed airways. In this case the aider can remove the push-on part 103 from the flow tube 2 and fasten it to their arm with the help of the arm fastening device 130. The penetration depth is now registered with the help of the acceleration sensor integrated into the housing 123. If the airways are not obstructed, the mass or volumetric flow of the air flowing out of the person can be continuously registered with every compression of the person's thorax and displayed on the display device. The mass or volumetric flow is a measure of the penetration depth in the cardiac massage. The aider learns from the display device whether the penetration depth was too low, sufficient or too high. They can modify the penetration depth accordingly in the next compression.
(33) All features of the invention can be material to the invention both individually and in any combination.
REFERENCE NUMBERS
(34) 1 Device for artificial respiration in emergencies
(35) 2 Flow tube
(36) 3 Push-on part
(37) 4 Longitudinal axis
(38) 5 End of the flow tube
(39) 6 End of the flow tube
(40) 7 First face end of the flow tube
(41) 8 Second face end of the flow tube
(42) 9 Sensor section
(43) 10 Sensor
(44) 10a Sensor fixture device
(45) 11 Sensor circuit board
(46) 12 Sensor sleeve
(47) 13 Sensor sleeve
(48) 14 Sensor opening
(49) 15 Side wall
(50) 16 Side wall
(51) 17 Side wall
(52) 18 Side wall
(53) 19 First filter
(54) 20 Second filter
(55) 21 Sleeve
(56) 22 Sleeve
(57) 23 Housing
(58) 24 Side wall
(59) 25 Side wall
(60) 26 Side wall
(61) 27 Circuit board
(62) 28 Circuit board
(63) 29 Connector socket
(64) 30 Cover
(65) 31 Outer housing part
(66) 32 Outer housing part
(67) 33 Handle element
(68) 34 Handle element
(69) 35 Grip recess
(70) 36 Grip recess
(71) 40 Respiratory mask
(72) 41 Mouthpiece
(73) 42 Elastic edge
(74) 43 Strap
(75) 44 Strap
(76) 101 Device for artificial respiration in emergencies
(77) 103 Push-on part
(78) 123 Housing
(79) 124 Output device
(80) 125 Input device
(81) 126 Optically active surface
(82) 127 Handle element
(83) 128 Recess
(84) 129 Arm
(85) 130 Arm fastening device