WO2022138083A1 - Inhalateur thérapeutique - Google Patents

Inhalateur thérapeutique Download PDF

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Publication number
WO2022138083A1
WO2022138083A1 PCT/JP2021/044547 JP2021044547W WO2022138083A1 WO 2022138083 A1 WO2022138083 A1 WO 2022138083A1 JP 2021044547 W JP2021044547 W JP 2021044547W WO 2022138083 A1 WO2022138083 A1 WO 2022138083A1
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WO
WIPO (PCT)
Prior art keywords
treatment
history information
cleaning
nebulizer
operation history
Prior art date
Application number
PCT/JP2021/044547
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English (en)
Japanese (ja)
Inventor
麻 平澤
賢吾 西山
友香 田邊
真郎 前田
美由紀 足達
Original Assignee
オムロンヘルスケア株式会社
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Application filed by オムロンヘルスケア株式会社 filed Critical オムロンヘルスケア株式会社
Publication of WO2022138083A1 publication Critical patent/WO2022138083A1/fr

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    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61M—DEVICES 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
    • A61M11/00—Sprayers or atomisers specially adapted for therapeutic purposes

Definitions

  • the present invention relates to a therapeutic inhaler.
  • Patent Document 1 describes a tubular container having a liquid pool capable of accommodating the chemical liquid and an outlet for opening the liquid pool to the outside, and a chemical liquid provided in the tubular container to atomize and atomize the chemical liquid.
  • a nebulizer equipped with an ultrasonic pump that sprays through a spout is described. This nebulizer is configured to be able to clean the spray mechanism by discarding the chemical liquid in the liquid pool, injecting distilled water for cleaning or the like into the liquid pool, and spraying the distilled water.
  • Patent Document 2 describes a mist generator that sends out a liquid such as water or lotion as a fine mist.
  • the cleaning switch is operated to reverse the operation of the chemical spraying mechanism to clean the spraying mechanism with cleaning water.
  • Treatment using a therapeutic inhaler such as a nebulizer configured to be able to inhale the atomized drug solution is required to be performed at the frequency specified by the doctor.
  • a therapeutic inhaler such as a nebulizer configured to be able to inhale the atomized drug solution
  • one treatment using a therapeutic inhaler means that an operation of inhaling the same type of drug for a predetermined time (for example, 5 minutes or the like) is performed.
  • a predetermined time for example, 5 minutes or the like
  • the liquid atomized by the atomizing portion is changed from a chemical solution to a cleaning solution, and the cleaning solution is atomized in that state to atomize.
  • a configuration for cleaning the part is assumed.
  • the cleaning operation of the atomized portion and the atomization operation of the chemical solution by the atomized portion cannot be distinguished, it becomes difficult to determine whether or not the treatment is performed at an appropriate frequency.
  • An object of the present invention is to provide a therapeutic inhaler capable of appropriately managing the history of treatment.
  • the processor is a therapeutic inhaler that changes the content of the management depending on whether the first process is performed or the second process is performed.
  • the information to be added to the operation history information is changed depending on whether the cleaning start operation is received or the treatment start operation is received, and then the information is transmitted to the external device or the treatment start operation is performed. It is possible to send the operation history information to an external device only when it is received. This makes it possible to manage the state in which the atomized portion is operated for cleaning and the state in which the atomized portion is operated for treatment. As a result, the frequency of treatment using the therapeutic inhaler can be accurately grasped, which can be useful for determining the treatment policy.
  • the processor transmits the operation history information of the atomizing unit operated by the first process to an external device, and when the second process is performed, the first process is performed.
  • a therapeutic inhaler that omits transmission of the operation history information of the atomized portion operated by the treatment to the external device.
  • the operation history information of the atomizing part for cleaning is not transmitted to the external device. Therefore, in the external device, only the operation history information of the atomized portion operated for the treatment is collected. By using this collected information, it becomes possible to accurately grasp the frequency of treatment using the therapeutic inhaler.
  • the therapeutic inhaler according to the above.
  • the processor can distinguish between the first operation history information of the atomization unit operated by the first process and the second operation history information of the atomization unit operated by the second process in an identifiable format.
  • a therapeutic inhaler that sends to an external device.
  • the therapeutic inhaler according to the above.
  • the processor is a therapeutic inhaler that adds information indicating that the second operation history information is an operation for cleaning and transmits the information to the external device.
  • the therapeutic inhaler is a therapeutic inhaler that adds information indicating that the first operation history information is an operation for treatment and transmits the information to the external device.
  • the therapeutic inhaler according to any one of (1) to (5).
  • the processor is a therapeutic inhaler that stops the atomizing portion after a predetermined time elapses when the atomizing portion is operated in response to the cleaning start operation.
  • the atomized portion when the atomized portion is washed, the atomized portion will not be operated beyond the predetermined time. As a result, it is possible to prevent the atomized portion from being operated more than necessary during cleaning, and to improve the durability of the device.
  • the therapeutic inhaler according to any one of (1) to (6).
  • the operation member is a therapeutic inhaler including a first operation member capable of performing the treatment start operation and a second operation member capable of performing the cleaning start operation.
  • FIG. 6 It is a schematic diagram which shows the schematic structure of the treatment management system. It is an exploded perspective view of the nebulizer shown in FIG. It is a vertical sectional view of the nebulizer shown in FIG. 2 as seen from the right side (direction indicated by arrow A in FIG. 2). It is a schematic diagram explaining the use state of the nebulizer shown in FIG. It is a figure which shows the block structure of the nebulizer shown in FIG. 6 is a timing chart for explaining the operation of the nebulizer control unit shown in FIG. 5 during treatment control. It is a timing chart for demonstrating the operation at the time of cleaning control of the nebulizer control unit shown in FIG.
  • FIG. 6 is a timing chart for explaining a modified example of the operation of the nebulizer control unit during treatment control shown in FIG. 5. It is a timing chart for demonstrating the modification of the operation at the time of cleaning control of the nebulizer control unit shown in FIG.
  • the nebulizer according to the embodiment of the present invention has a treatment mode in which a drug solution is atomized by an atomizing portion and a respiratory disease such as asthma is treated by inhaling the atomized drug solution, and a cleaning solution is atomized instead of the drug solution. It is equipped with a cleaning mode that cleans the atomized part by atomizing it by the part. These modes are changed by operating the operating member provided on the nebulizer.
  • the nebulizer is further configured to be communicable with an external device, has a function of managing the transmission of the operation history information of the atomizing unit to the external device, and changes the content of this management according to the mode.
  • the nebulizer transmits the operation history information of the atomized portion operated in the treatment mode to the external device, and does not transmit the operation history information of the atomized portion operated in the cleaning mode to the external device.
  • the operation history information of the atomized portion operated for the treatment is collected in the external device. Therefore, by using this collected operation history information, it becomes possible to accurately grasp the frequency and the like of the treatment performed using the nebulizer, which can be useful for the doctor to decide the treatment policy.
  • the details of the embodiment of the treatment management system including the nebulizer will be described.
  • FIG. 1 is a schematic diagram showing a schematic configuration of the treatment management system 100.
  • the treatment management system 100 includes a nebulizer 1 as a therapeutic inhaler for treating a respiratory disease by inhaling a sprayed drug solution, and an electron possessed by a user of the nebulizer 1 or a related person (for example, a parent of the user). It includes a device 3 and a management server 6.
  • the electronic device 3 is an electronic device having a communication function such as a personal computer, a smartphone, or a tablet terminal.
  • the electronic device 3 is configured to be able to communicate with the management server 6 via a network 4 such as the Internet.
  • the electronic device 3 is configured to be communicable with the nebulizer 1 based on a short-range communication standard such as Bluetooth (registered trademark) or Wi-Fi.
  • the treatment management application provided by the operator of the treatment management system 100 is installed in the electronic device 3.
  • This treatment management application information transmission / reception between the nebulizer 1 and the electronic device 3, information transmission from the electronic device 3 to the management server 6, and an electronic device for display data generated by the management server 6 are performed. It is possible to browse by 3.
  • the management server 6 includes a communication interface (IF) 61 for communicating with a device connected to the network 4, a server control unit 62, and a database 63.
  • the database 63 may be a storage externally attached to the management server 6 or a network storage connected to the network 4.
  • the server control unit 62 controls the entire management server 6 in an integrated manner, and stores a processor such as a CPU (Central Processing Unit) that executes a program and performs processing, and a ROM (Read) that stores the program or the like executed by this processor. Only Memory) and RAM (Random Access Memory) as a work memory are included.
  • a processor such as a CPU (Central Processing Unit) that executes a program and performs processing
  • ROM Read
  • Only Memory and RAM Random Access Memory
  • the structure of the processor described in the present specification is an electric circuit in which circuit elements such as semiconductor elements are combined.
  • the server control unit 62 acquires the information transmitted from the nebulizer 1 to the electronic device 3 and transferred from the electronic device 3 via the communication interface 61, and records the acquired information in the database 63. By processing the information recorded in the database 63, the server control unit 62 processes the treatment results such as the timing (treatment timing) of the treatment performed using the nebulizer 1 and the time (treatment time) of the treatment. Generate display data to display.
  • the server control unit 62 requests viewing of this display data from the electronic device 3 or another electronic device connected to the network 4 (for example, a device operated by a doctor in charge of examining the user of the nebulizer 1). Upon receiving the image, the image based on the display data is controlled to be displayed on the requesting electronic device.
  • FIG. 2 is an exploded perspective view of the nebulizer 1 shown in FIG.
  • FIG. 3 is a vertical cross-sectional view of the nebulizer 1 shown in FIG. 2 as viewed from the right side (direction indicated by an arrow A in FIG. 2).
  • the nebulizer 1 includes a main body lower portion 11 having a substantially elliptical columnar outer shape, and a main body upper portion 12 mounted detachably fitted to the main body lower portion 11 from above. It includes a main body 10, a mounting member 20 mounted on the main body upper portion 12, and a cap member 30 configured to be openable and closable with respect to the main body upper portion 12.
  • the front half portion 12F of the main body upper portion 12 has a substantially columnar outer shape
  • the latter half portion 12R of the main body upper portion 12 has a substantially trapezoidal columnar outer shape.
  • the lower portion 11 of the main body is provided with an operation member 50 including a start / end button 51 constituting the first operation member and a cleaning button 54 constituting the second operation member.
  • a recess 16 having a substantially circular planar shape opened upward so as to receive the mounting member 20 is provided on the upper surface of the front half portion 12F of the upper part 12 of the main body.
  • the recess 16 has a bottom surface 16b that is inclined with respect to the vertical direction (vertical direction) of the main body 10, and a side surface 16c that is continuous with the bottom surface 16b and gradually opens upward.
  • the ridges 19f and 19r are provided in a specific direction (front side, rear side in this example) at the edge portion 15 around the recess 16.
  • the ridge 19f on the front side has a planar shape protruding in an arc shape toward the center of the recess 16.
  • the ridge 19r on the rear side has a planar shape recessed in an arc shape when viewed from the center of the recess 16.
  • the ridges 19f and 19r are planned to be fitted to the flange portion 24 of the mounting member 20.
  • a packing 29 made of an annular elastic body is provided on the side surface 16c of the recess 16 so as to surround and contact the side wall portion 23 of the mounting member 20 in the circumferential direction.
  • a vibrating portion 40 is provided at a position corresponding to the recess 16 inside the front half portion 12F of the main body upper portion 12.
  • the vibrating portion 40 includes an ultrasonic vibrator 41 arranged at a position downwardly separated from the recess 16, a vibrating surface 43 horizontally arranged at a position corresponding to the bottom surface 16b of the recess 16, and an ultrasonic vibrator 41. It includes a horn 42 that is arranged between the vibration surface 43 and amplifies the vibration of the ultrasonic vibrator 41 and transmits the vibration to the vibration surface 43.
  • the drive voltage for the ultrasonic vibrator 41 is supplied from the lower part 11 of the main body via the contact electrode provided between the upper part 12 of the main body and the lower part 11 of the main body.
  • a liquid storage portion 17 having a substantially semicircular planar shape is provided in the latter half portion 12R of the upper portion 12 of the main body.
  • the liquid storage unit 17 has a bottom surface 17b that gradually becomes shallower toward the front side.
  • a liquid supply passage 18 for supplying a liquid (chemical solution) from the liquid storage unit 17 toward the vibrating surface 43 of the vibrating unit 40 is provided so as to be connected to the front surface side portion of the liquid storage unit 17.
  • the liquid storage unit 17 is open upward. Therefore, the user can put a liquid such as a chemical solution into the liquid storage unit 17 from above.
  • a cap member 30 forming a lid is connected to the upper edge of the latter half portion 12R of the main body upper portion 12 so as to be rotatable with respect to the main body upper portion 12 via a hinge 38.
  • the cap member 30 includes a latter half portion 30R arranged on the side close to the hinge 38 and having a substantially trapezoidal planar shape, and a front half portion 30F which is connected to the latter half portion 30R and has a substantially circular planar shape.
  • the portion 33 is provided so as to project.
  • a mesa portion 34 having a substantially trapezoidal planar shape corresponding to the planar shape of the liquid storage portion 17 is provided on the side of the latter half portion 30R of the cap member 30 facing the upper surface of the upper portion 12 of the main body.
  • the protrusion 33 works to position the mounting member 20.
  • the mesa section 34 closes the upper portion of the liquid storage section 17 to prevent the chemical solution from overflowing from the liquid storage section 17.
  • the center of the front half portion 30F of the cap member 30 is an opening 30o to which a mouthpiece or the like should be attached.
  • the leading edge 30Fe (opposite to the hinge 38) of the front half portion 30F of the cap member 30 is provided with an engaging protrusion 31 protruding inward.
  • the front half portion 12F of the upper portion 12 of the main body is provided with an engaging protrusion 14 projecting outward (forward) from the front end.
  • the mounting member 20 is mounted in the recess 16 of the upper part 12 of the main body when the nebulizer 1 is used.
  • the mounting member 20 should be connected to the flat film-like sheet 21 that should face the vibration surface 43, the bottom plate portion 22 that supports the sheet 21, and the outer edge of the bottom plate portion 22, and should face the side surface 16c of the recess 16.
  • the sheet 21 is attached to the lower surface of the bottom plate portion 22 by adhesion or welding.
  • the substantially central region of the sheet 21 constitutes the mesh portion 21a.
  • a user who intends to use the nebulizer 1 has a recess 16 having a shape that opens upward of the main body 10 with the cap member 30 open to the main body 10, as shown by an arrow D in FIG.
  • the mounting member 20 having the mesh portion 21a is mounted. With the mounting member 20 mounted, the user rotates and closes the cap member 30 with respect to the main body 10 (main body upper portion 12) via the hinge 38. Then, the engaging projection 31 of the cap member 30 engages with the engaging projection 14 of the upper portion 12 of the main body in the vertical direction. As a result, the cap member 30 is fixed to the upper portion 12 of the main body in a closed state. In this way, the nebulizer 1 is easily assembled. This state is called the assembled state.
  • nebulizer When using the nebulizer 1, the user previously puts a chemical solution in the liquid storage unit 17 of the upper part 12 of the main body. Then, as shown in FIG. 4, the user attaches, for example, the mouthpiece 80 to the opening 30o of the cap member 30 in the assembled state. Instead of the mouthpiece 80, an inhalation mask that covers the face of the user 99 may be worn.
  • the chemical solution is supplied from the liquid storage section 17 through the liquid supply path 18 toward the vibrating surface 43 of the vibrating section 40. That is, the chemical solution is supplied between the vibrating surface 43 and the mesh portion 21a.
  • the chemical solution is passed through the mesh portion 21a (more accurately, a plurality of through holes penetrating the sheet 21). 90 is atomized and spouts.
  • the vibrating portion 40 and the mesh portion 21a of the mounting member 20 constitute an atomizing unit (the atomizing unit 73 described later) for atomizing a liquid such as a chemical solution stored in the liquid storage unit 17.
  • the nebulizer 1 operates the atomizing unit 73 with a cleaning liquid such as tap water in the liquid storage unit 17 to atomize the cleaning liquid, thereby atomizing the atomizing unit 73 (more specifically, the vibration surface 43). And the mesh portion 21a) can be cleaned.
  • a cleaning liquid such as tap water in the liquid storage unit 17 to atomize the cleaning liquid, thereby atomizing the atomizing unit 73 (more specifically, the vibration surface 43).
  • the mesh portion 21a) can be cleaned.
  • FIG. 5 is a diagram showing a block configuration of the nebulizer 1.
  • the nebulizer 1 includes an operation member 50, a nebulizer control unit 71, an oscillation frequency generation unit 72, an atomization unit 73, a communication interface 74, and a notification unit 75.
  • the start / end button 51 included in the operation member 50 is a treatment start operation for instructing the nebulizer control unit 71 to start treatment (in other words, start of operation of the atomization unit 73) and an end of treatment (in other words, fog). It is a member capable of performing a treatment end operation instructing the nebulizer control unit 71 (stopping the operation of the chemical unit 73). For example, a short press operation of the start / end button 51 in a state where the atomizing unit 73 is not operating is a treatment start operation, and a short press operation of the start / end button 51 after the treatment start operation is a treatment end operation. ..
  • the start / end button 51 may be divided into two, a button for performing the treatment start operation and a button for performing the treatment end operation.
  • the cleaning button 54 included in the operation member 50 is a member capable of performing a cleaning start operation instructing the nebulizer control unit 71 to start cleaning the atomizing unit 73.
  • a short-pressing operation of the washing button 54 in a state where the atomizing unit 73 is not operating is called a washing start operation.
  • the oscillation frequency generation unit 72 applies an AC drive voltage to the ultrasonic vibrator 41 of the vibration unit 40 based on the control signal from the nebulizer control unit 71.
  • the state in which the driving voltage is applied to the ultrasonic vibrator 41 is referred to as the state in which the atomizing unit 73 is operating, and the state in which the driving voltage is not applied to the ultrasonic vibrator 41 is referred to as a state in which the atomizing unit 73 is operating. It is said that the atomization unit 73 is stopped.
  • the nebulizer control unit 71 is configured to include a processor such as a CPU, and performs various processes on this processor.
  • a processor such as a CPU
  • the nebulizer control unit 71 activates the atomization unit 73, and when the nebulizer control unit 71 detects the treatment end operation when the atomization unit 73 is operating.
  • Treatment control is performed to stop the atomizing unit 73.
  • the mode for controlling the treatment is the treatment mode described in the above outline.
  • the nebulizer control unit 71 handles the first timing (specifically, the date and time) when the treatment start operation is detected as the operation start timing of the atomization unit 73. Further, the nebulizer control unit 71 handles the second timing (specifically, the date and time) when the treatment end operation is detected as the operation end timing of the atomization unit 73. Further, the nebulizer control unit 71 handles the time from the first timing to the second timing as the operation time of the atomization unit 73. These first timing, second timing, and operation time each constitute operation history information of the atomizing unit 73 at the time of this treatment control.
  • the nebulizer control unit 71 When the nebulizer control unit 71 detects a cleaning start operation while the atomizing unit 73 is not operating, the nebulizer control unit 71 operates the atomizing unit 73, and a predetermined time (for example, 1 minute, etc.) has elapsed since the detection of the cleaning start operation. Then, the cleaning control for stopping the atomizing unit 73 is performed.
  • the mode for performing cleaning control is the cleaning mode described in the above outline.
  • the nebulizer control unit 71 may stop the atomization unit 73 if the treatment end operation is not detected for a predetermined time after the treatment start operation is detected.
  • the predetermined time in this case is set to a time longer than the above-mentioned predetermined time.
  • the user of the nebulizer 1 When the user of the nebulizer 1 performs his / her own treatment, he / she performs the treatment start operation with the drug solution charged into the liquid storage unit 17 and inhales the atomized drug solution. After that, the user performs a treatment end operation and ends the inhalation of the drug solution.
  • the user When cleaning the atomizing unit 73, the user performs a cleaning start operation with a cleaning liquid such as tap water charged into the liquid storage unit 17, and atomizes the cleaning liquid to clean the atomizing unit 73. I do.
  • the nebulizer control unit 71 When the nebulizer control unit 71 operates the atomization unit 73, the nebulizer control unit 71 manages the transmission of the operation history information of the atomization unit 73 regarding the operation to the electronic device 3.
  • the nebulizer control unit 71 manages the transmission of the operation history information of the atomization unit 73 regarding the operation to the electronic device 3.
  • FIG. 6 is a timing chart for explaining the operation of the nebulizer control unit 71 during treatment control.
  • the nebulizer control unit 71 activates the atomization unit 73 when the treatment start operation is detected at the timing t1.
  • the nebulizer control unit 71 detects the treatment end operation at the timing t2
  • the nebulizer control unit 71 stops the operation of the atomization unit 73 and generates the operation history information J1 regarding the operation of the atomization unit 73 started at the timing t1.
  • the nebulizer control unit 71 transmits the operation history information J1 to the electronic device 3 at the timing t3 after the atomization unit 73 is stopped.
  • the operation history information J1 is composed of, for example, a timing t1 (operation start timing) and a time between the timing t1 and the timing t2 (the operation time of the atomizing unit 73).
  • the operation history information J1 is composed of two timings t1 (operation start timing) and timing t2 (operation end timing), or a time (operation time) and timing t2 (operation end timing) between timing t1 and timing t2. It may be composed of two.
  • the operation history information J1 may further include information on the type of the chemical solution atomized by the atomizing unit 73.
  • the operating time of the atomizing unit 73 has a strong correlation with the amount of the drug solution inhaled by the user. Therefore, by referring to this operating time, it is possible to determine to some extent how much drug solution the user has inhaled.
  • the electronic device 3 that has received the operation history information J1 from the nebulizer 1 transfers the operation history information J1 to the management server 6.
  • this operation history information J1 is recorded in the database 63.
  • FIG. 7 is a timing chart for explaining the operation of the nebulizer control unit 71 during cleaning control.
  • the nebulizer control unit 71 operates the atomization unit 73 when the cleaning start operation is detected at the timing t4, and stops the operation of the atomization unit 73 when the timing t5 after the above-mentioned predetermined time elapses from the timing t4.
  • the nebulizer control unit 71 does not transmit the operation history information regarding the operation of the atomization unit 73 started at the timing t4 to the electronic device 3. That is, the operation history information of the atomizing unit 73 operated for cleaning is not transmitted to the management server 6. Therefore, in the management server 6, only the operation history information (the above-mentioned operation history information J1) of the atomizing unit 73 operated for the treatment is collected.
  • the nebulizer 1 of the treatment management system 100 transmits the operation history information J1 at the timing after the operation of the atomizing unit 73 is stopped. In this way, the operation history information J1 is transmitted in a state where the ultrasonic transducer 41 of the atomizing unit 73 is not operating, so that the transmission is performed without being affected by the operating noise of the atomizing unit 73. It can be done stably. Therefore, the operation history information J1 can be transmitted to the management server 6 without omission, and the treatment can be managed accurately.
  • the operation history information J1 may include at least information that can specify the treatment timing (for example, the operation start timing of the atomization unit 73 or the operation end timing of the atomization unit 73). As described above, when the operation history information J1 includes the operation time, the doctor can confirm whether or not an appropriate amount of the drug solution is aspirated at each treatment. As a result, it can be useful for deciding the treatment policy.
  • the treatment timing for example, the operation start timing of the atomization unit 73 or the operation end timing of the atomization unit 73.
  • the nebulizer 1 may transmit the operation history information of the atomizing unit 73 to the electronic device 3 (management server 6) in each of the case where the treatment control is performed and the case where the cleaning control is performed.
  • FIG. 8 is a timing chart for explaining a modified example of the operation of the nebulizer control unit 71 during treatment control.
  • FIG. 9 is a timing chart for explaining a modified example of the operation of the nebulizer control unit 71 during cleaning control.
  • the nebulizer control unit 71 operates the atomization unit 73 at the timing t1 and stops the operation of the atomization unit 73 at the timing t2. Further, when the nebulizer control unit 71 detects the treatment end operation at the timing t2, the nebulizer control unit 71 generates the same operation history information J1 (first operation history information) as described above, and adds a default treatment ID to the operation history information J1. do.
  • the treatment ID is identification information indicating that the operation is for treatment. Then, the nebulizer control unit 71 transmits the operation history information J1 to which the treatment ID is added to the electronic device 3 at the timing t3 after the atomization unit 73 is stopped.
  • the nebulizer control unit 71 operates the atomization unit 73 when the cleaning start operation is detected at the timing t4, and stops the operation of the atomization unit 73 at the timing t5. Further, when the nebulizer control unit 71 stops the operation of the atomizing unit 73 at the timing t5, the operation history information J2 (second operation history information) is generated, and the cleaning ID is added to the operation history information J2.
  • the cleaning ID is identification information indicating that the operation is for cleaning.
  • the operation history information J2 includes, for example, a timing t4 (operation start timing) and a time from the timing t4 until the atomization unit 73 stops (operation time).
  • the nebulizer control unit 71 transmits the operation history information J2 to which the cleaning ID is added to the electronic device 3 at the timing t6 after the atomization unit 73 is stopped.
  • the electronic device 3 that has received the operation history information J1 and J2 from the nebulizer 1 transfers the operation history information J1 and J2 to the management server 6.
  • the operation history information J1 and J2 are recorded in the database 63.
  • identification information is added to the first operation history information of the atomizing unit 73 operated for treatment and the second operation history information of the atomizing unit 73 operated for cleaning. In this state, it is transmitted to the management server 6. Therefore, by referring to this identification information, only the operation history information for treatment can be extracted from a large number of operation history information recorded in the database 63. Then, by referring to the data based on the extracted operation history information, it becomes possible to accurately confirm the treatment timing, treatment time, etc. of the treatment using the nebulizer 1.
  • the doctor can also determine that the symptom has not improved due to the fact that the cleaning is not performed regularly.
  • the nebulizer control unit 71 adds a treatment ID to the operation history information J1 and transmits the operation history information J2 to the management server 6 without adding identification information such as a cleaning ID to the operation history information J2. You may do so. Even in this way, only the operation history information J1 for treatment can be extracted from a large number of operation history information recorded in the database 63.
  • the nebulizer control unit 71 adds a cleaning ID to the operation history information J2 and transmits the operation history information J1 to the management server 6 without adding identification information such as a treatment ID to the operation history information J1. You may do so. Even in this way, only the operation history information J1 for treatment can be extracted from a large number of operation history information recorded in the database 63.
  • the electronic device 3 may be omitted, and the nebulizer 1 and the management server 6 may communicate with each other via the network 4. Further, the management server 6 may be omitted, and the function of the management server 6 may be realized by the treatment management application installed in the electronic device 3. That is, the electronic device 3 may be configured to record and manage the operation history information.
  • Treatment management system 100 Treatment management system 1 Nebulizer 50 Operation member 51 Start / end button 54 Wash button 71 Nebulizer control unit 73 Atomization unit 3 Electronic device 4 Network 6 Management server

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  • Health & Medical Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Anesthesiology (AREA)
  • Biomedical Technology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Hematology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Special Spraying Apparatus (AREA)

Abstract

La présente divulgation concerne un inhalateur thérapeutique capable de gérer de manière appropriée un historique de traitement.　Le nébuliseur (1) est équipé d'une opération de démarrage de traitement pour indiquer le démarrage du traitement, d'un élément d'actionnement (50) capable de réaliser une opération de démarrage de nettoyage pour indiquer le démarrage de nettoyage d'une unité d'atomisation (73), et d'une unité de commande de nébuliseur (71) pour mettre en œuvre un premier processus destiné à activer l'unité d'atomisation (73) en réponse à l'opération de démarrage de traitement, un deuxième processus destiné à activer l'unité d'atomisation (73) en réponse à l'opération de démarrage de nettoyage, et un troisième processus destiné à gérer la transmission des informations d'historique d'activation de l'unité d'atomisation (73) à un serveur de gestion (6). L'unité de commande de nébuliseur (71) modifie le contenu de la gestion ci-dessus en fonction de la mise en œuvre du premier processus ou du deuxième processus.
PCT/JP2021/044547 2020-12-23 2021-12-03 Inhalateur thérapeutique WO2022138083A1 (fr)

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Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2014018794A (ja) * 2012-08-08 2014-02-03 Hitachi Maxell Ltd ミスト発生装置
JP2019504696A (ja) * 2016-02-08 2019-02-21 パリ ファーマ ゲーエムベーハー 医療評価装置
JP2020500639A (ja) * 2016-12-09 2020-01-16 トゥルーデル メディカル インターナショナル スマートネブライザ

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2014018794A (ja) * 2012-08-08 2014-02-03 Hitachi Maxell Ltd ミスト発生装置
JP2019504696A (ja) * 2016-02-08 2019-02-21 パリ ファーマ ゲーエムベーハー 医療評価装置
JP2020500639A (ja) * 2016-12-09 2020-01-16 トゥルーデル メディカル インターナショナル スマートネブライザ

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