WO2022131436A1 - Method, device, and computer program product for providing notification according to period of use of medicine injection device - Google Patents

Method, device, and computer program product for providing notification according to period of use of medicine injection device Download PDF

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Publication number
WO2022131436A1
WO2022131436A1 PCT/KR2021/000317 KR2021000317W WO2022131436A1 WO 2022131436 A1 WO2022131436 A1 WO 2022131436A1 KR 2021000317 W KR2021000317 W KR 2021000317W WO 2022131436 A1 WO2022131436 A1 WO 2022131436A1
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WO
WIPO (PCT)
Prior art keywords
injection device
period
drug injection
time point
drug
Prior art date
Application number
PCT/KR2021/000317
Other languages
French (fr)
Korean (ko)
Inventor
전용호
이동민
Original Assignee
이오플로우(주)
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 이오플로우(주) filed Critical 이오플로우(주)
Priority to CN202180003018.5A priority Critical patent/CN114945989A/en
Publication of WO2022131436A1 publication Critical patent/WO2022131436A1/en

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    • GPHYSICS
    • G16INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR SPECIFIC APPLICATION FIELDS
    • G16HHEALTHCARE INFORMATICS, i.e. INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR THE HANDLING OR PROCESSING OF MEDICAL OR HEALTHCARE DATA
    • G16H20/00ICT specially adapted for therapies or health-improving plans, e.g. for handling prescriptions, for steering therapy or for monitoring patient compliance
    • G16H20/10ICT specially adapted for therapies or health-improving plans, e.g. for handling prescriptions, for steering therapy or for monitoring patient compliance relating to drugs or medications, e.g. for ensuring correct administration to patients
    • G16H20/17ICT specially adapted for therapies or health-improving plans, e.g. for handling prescriptions, for steering therapy or for monitoring patient compliance relating to drugs or medications, e.g. for ensuring correct administration to patients delivered via infusion or injection
    • 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
    • A61M5/00Devices for bringing media into the body in a subcutaneous, intra-vascular or intramuscular way; Accessories therefor, e.g. filling or cleaning devices, arm-rests
    • A61M5/14Infusion devices, e.g. infusing by gravity; Blood infusion; Accessories therefor
    • A61M5/142Pressure infusion, e.g. using pumps
    • 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
    • A61M5/00Devices for bringing media into the body in a subcutaneous, intra-vascular or intramuscular way; Accessories therefor, e.g. filling or cleaning devices, arm-rests
    • A61M5/14Infusion devices, e.g. infusing by gravity; Blood infusion; Accessories therefor
    • A61M5/142Pressure infusion, e.g. using pumps
    • A61M5/14244Pressure infusion, e.g. using pumps adapted to be carried by the patient, e.g. portable on the body
    • 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
    • A61M5/00Devices for bringing media into the body in a subcutaneous, intra-vascular or intramuscular way; Accessories therefor, e.g. filling or cleaning devices, arm-rests
    • A61M5/14Infusion devices, e.g. infusing by gravity; Blood infusion; Accessories therefor
    • A61M5/168Means for controlling media flow to the body or for metering media to the body, e.g. drip meters, counters ; Monitoring media flow to the body
    • 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
    • A61M5/00Devices for bringing media into the body in a subcutaneous, intra-vascular or intramuscular way; Accessories therefor, e.g. filling or cleaning devices, arm-rests
    • A61M5/14Infusion devices, e.g. infusing by gravity; Blood infusion; Accessories therefor
    • A61M5/168Means for controlling media flow to the body or for metering media to the body, e.g. drip meters, counters ; Monitoring media flow to the body
    • A61M5/16831Monitoring, detecting, signalling or eliminating infusion flow anomalies
    • 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
    • A61M5/00Devices for bringing media into the body in a subcutaneous, intra-vascular or intramuscular way; Accessories therefor, e.g. filling or cleaning devices, arm-rests
    • A61M5/14Infusion devices, e.g. infusing by gravity; Blood infusion; Accessories therefor
    • A61M5/168Means for controlling media flow to the body or for metering media to the body, e.g. drip meters, counters ; Monitoring media flow to the body
    • A61M5/172Means for controlling media flow to the body or for metering media to the body, e.g. drip meters, counters ; Monitoring media flow to the body electrical or electronic
    • GPHYSICS
    • G08SIGNALLING
    • G08BSIGNALLING OR CALLING SYSTEMS; ORDER TELEGRAPHS; ALARM SYSTEMS
    • G08B21/00Alarms responsive to a single specified undesired or abnormal condition and not otherwise provided for
    • G08B21/18Status alarms
    • 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
    • A61M5/00Devices for bringing media into the body in a subcutaneous, intra-vascular or intramuscular way; Accessories therefor, e.g. filling or cleaning devices, arm-rests
    • A61M5/14Infusion devices, e.g. infusing by gravity; Blood infusion; Accessories therefor
    • A61M5/142Pressure infusion, e.g. using pumps
    • A61M2005/14208Pressure infusion, e.g. using pumps with a programmable infusion control system, characterised by the infusion program
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61MDEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M2205/00General characteristics of the apparatus
    • A61M2205/18General characteristics of the apparatus with alarm
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61MDEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M2205/00General characteristics of the apparatus
    • A61M2205/27General characteristics of the apparatus preventing use
    • A61M2205/276General characteristics of the apparatus preventing use preventing unwanted use
    • 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
    • A61M2205/52General characteristics of the apparatus with microprocessors or computers with memories providing a history of measured variating parameters of apparatus or patient

Definitions

  • the present disclosure provides a method, an apparatus, and a computer program product for providing a notification according to the period of use of a drug injection device.
  • Diabetes mellitus is a metabolic disorder that causes signs that blood sugar is outside the normal range due to insufficient insulin secretion or normal function. Diabetes mellitus is a complex disease that has the potential to affect individual tissues of the human body due to complications such as blindness, renal failure, heart failure, and neuropathy, and the number of diabetic patients is increasing every year.
  • An object of the present invention is to provide a method, an apparatus and a computer program product for providing a notification according to the period of use of a drug injection device.
  • the technical problem to be achieved by this embodiment is not limited to the technical problems as described above, and other technical problems may be inferred from the following embodiments.
  • a first aspect of the present disclosure is a method for providing a notification according to the period of use of a drug injection device, wherein the drug injection device is operated in an inactive mode in an active mode ( determining the time to switch to active mode) as the time to start using; based on the usable period of the drug injection device and a user-set time, providing an imminent expiration notification indicating that the expiration date of the use period of the drug injection device is imminent at a first time point when a predetermined period has elapsed from the start of use; and providing an expiration notice indicating that the use period of the drug injection device has expired at a second time point when the usable period has elapsed from the start of use.
  • a second aspect of the present disclosure provides an apparatus for providing a notification according to a period of use of a drug injection device, comprising: a memory in which at least one program is stored; and a processor that performs an operation by executing the at least one program, wherein the processor determines a time when the drug injection device is switched from an inactive mode to an active mode as a use start time, and the drug injection device can be used Based on a period and a user set time, an imminent expiration notification indicating that the expiration of the use period of the drug injection device is imminent is provided at a first time point when a predetermined period has elapsed from the start of use, and the use is possible from the start of use
  • a device may be provided that provides an expiration notification indicating that the period of use of the drug injection device has expired at a second time point when the period has elapsed.
  • a third aspect of the present disclosure includes the steps of: determining a time when the drug injection device is switched from an inactive mode to an active mode as a start time of use; providing a notification of imminent replacement of the drug injection device at a first time point when a predetermined period has elapsed from the start time of use, based on a usable period of the drug injection device and a user-set time; and providing an expiration notification that the use period of the drug injection device has expired at a second time point when the usable period has passed from the start of use; one or more computer-readable recording media storing a program to perform A computer program product comprising the may be provided.
  • convenience of use is provided by determining the period of use of the drug injection device based on the storage capacity and the average daily dose of the drug injection device, and providing a notification according to the period of use can do.
  • the drug while the drug is injected from the drug injection device to the user, by determining the period of use of the drug injection device based on the material of the object maintained in the state inserted into the user's body, the drug A method for safely using an injection device may be provided.
  • FIG. 1 is a block diagram of an insulin management system including a user terminal, a controller, and a drug injection device.
  • 2A to 2B are exemplary views for explaining a method of setting a drug injection amount calculator according to an embodiment.
  • FIG. 3 is a diagram illustrating an internal configuration of a drug injection device according to an embodiment.
  • FIG. 4 is a view for explaining an example of providing a notification according to the period of use of the drug injection device according to an embodiment.
  • 5 is a view for explaining an example of providing a notification according to the period of use of the drug injection device according to an embodiment.
  • FIG. 6 is a flowchart of a method of providing a notification according to the period of use of the drug injection device according to an embodiment.
  • a time when the drug injection device is switched from an inactive mode to an active mode may be determined as a start time of use.
  • an imminent expiration notification indicating that the expiration of the use period of the drug injection device is imminent may be provided at a first time point after a predetermined period from the start of use.
  • an expiration notification indicating that the use period of the drug injection device has expired may be provided at a second time point when the usable period has elapsed from the start of use.
  • FIG. 1 is a block diagram of an insulin management system including a user terminal, a controller, and a drug injection device.
  • the user terminal 1000 refers to a communication terminal capable of using a web service in a wired/wireless communication environment.
  • the user terminal 1000 may include a smartphone, a tablet PC, a PC, a smart TV, a mobile phone, a personal digital assistant (PDA), a laptop, a media player, a micro server, a global positioning system (GPS) device, an e-book terminal, It may be a terminal for digital broadcasting, a navigation system, a kiosk, an MP3 player, a digital camera, a home appliance, a device equipped with a camera, and other mobile or non-mobile computing devices.
  • PDA personal digital assistant
  • GPS global positioning system
  • the user terminal 1000 may be a wearable device such as a watch, glasses, a hair band, and a ring having a communication function and a data processing function.
  • a terminal equipped with an application capable of Internet communication may be borrowed without limitation.
  • the user terminal 1000 may be connected one-to-one with the pre-registered controller 2000 . Also, the user terminals 1000 may receive data from the controller 2000 in order to prevent control from an external device. The user terminal 1000 may transmit setting information, for example, system time information, to the controller 2000 within a preset range.
  • the controller 2000 performs a function of transmitting and receiving data to and from the drug injection device 3000 , and transmits a control signal related to injection of a drug such as insulin to the drug injection device 3000 , and blood glucose from the drug injection device 3000 . It is possible to receive a control signal related to the measurement of a biological value, such as.
  • the controller 2000 may transmit an instruction request to measure the user's current state to the drug injection device 3000 , and receive measurement data from the drug injection device 3000 in response to the instruction request.
  • the drug injection device 3000 also performs a function of measuring the user's blood sugar value, blood pressure, heart rate, etc., but should be injected into the user insulin, glucagon, anesthetic, analgesic, dopamine, growth hormone, smoking cessation aid It also performs the function of injecting drugs, such as.
  • the drug injection device 3000 may further include a storage unit for storing a substance to be periodically injected to the user, and an injection amount to be injected may be controlled to be injected from the storage unit according to an injection signal generated by the controller.
  • the drug injection device 3000 may transmit information such as a measurement value and an injection amount to the controller 2000 .
  • the drug injection device 3000 may transmit a device status message, a biometric value measurement message, a drug injection message, and the like to the controller 2000 .
  • the drug injection device 3000 may transmit a device status message including information on the remaining battery capacity of the device, whether the device is booted successfully, whether the injection is successful, and the like to the controller 2000 .
  • Messages transmitted to the controller may be transmitted to the user terminal 1000 via the controller 2000 .
  • the controller 2000 may transmit improved data obtained by processing the received messages to the user terminal 1000 .
  • the drug injection device 3000 may also be implemented to communicate only with a pre-registered controller.
  • the drug injection device 3000 includes a hardware measuring device that performs a function of measuring a user's blood sugar level, blood pressure, heart rate, etc., and a function of injecting drugs such as insulin, glucagon, anesthetic, etc. It can be divided into an injection device that performs. That is, the measuring device and the injection device may exist independently.
  • the controller 2000 may be respectively connected to the injection device and the measurement device to generate and provide a control signal for the injection device based on a measurement value measured by the measurement device.
  • a network includes a local area network (LAN), a wide area network (WAN), a value added network (VAN), a mobile radio communication network, a satellite communication network, and their It is a data communication network in a comprehensive sense that includes a mutual combination and enables each network constituent entity to communicate smoothly with each other, and may include a wired Internet, a wireless Internet, and a mobile wireless communication network.
  • LAN local area network
  • WAN wide area network
  • VAN value added network
  • mobile radio communication network a mobile radio communication network
  • satellite communication network and their It is a data communication network in a comprehensive sense that includes a mutual combination and enables each network constituent entity to communicate smoothly with each other, and may include a wired Internet, a wireless Internet, and a mobile wireless communication network.
  • wireless communication is, for example, wireless LAN (Wi-Fi), Bluetooth, Bluetooth low energy, Zigbee, WFD (Wi-Fi Direct), UWB (ultra wideband), infrared communication (IrDA, infrared Data Association), NFC (Near Field Communication), etc. may be there, but is not limited thereto.
  • 2A to 2B are exemplary views for explaining a method of setting a drug injection amount calculator according to an embodiment.
  • a drug injection amount calculator may be mounted on the user terminal 1000 , the controller 2000 , or the drug injection device 3000 of FIG. 1 .
  • the drug injection amount calculator may be a calculator for calculating the amount of insulin to be injected to the user separately from the basal injection.
  • a medication dose calculator for example, can calculate the amount of insulin needed to lower blood sugar, which rises due to eating food or snacks.
  • the drug injection amount calculator may calculate the amount of insulin required to bring the high blood sugar into the normal blood sugar range.
  • insulin injected when food intake or high blood sugar needs to be lowered may be referred to as a bolus.
  • the drug injection amount calculator may be referred to as a bolus calculator, and the bolus calculator may calculate a bolus injection amount.
  • the bolus injection amount may be determined by various values.
  • the bolus injection amount is the current blood glucose level, carbohydrate-to-insulin ratio, correction factor, target blood glucose level, the amount of insulin remaining in body activation time during the previous bolus injection (Insulin On Board (IOB), Bolus on Board ( BOB) or Active Insulin), the correction threshold, the amount of activity, and the type and amount of food consumed.
  • IOB Insulin On Board
  • BOB Bolus on Board
  • Active Insulin Active Insulin
  • the correction factor is a measure of the blood sugar level that 1Unit of bolus insulin can lower.
  • the range of the correction factor is 1 ⁇ 400mg/dl/U, and it can be adjusted by 1mg/dl/U.
  • the calibration threshold may mean a maximum blood sugar level at which it is determined that insulin injection is necessary for blood sugar control.
  • the bolus calculator may calculate the bolus injection amount based on the user's individual bolus profile setting value, the current blood sugar value, the amount of carbohydrate consumed, and the remaining amount of insulin in the body (IOB).
  • the bolus profile setting value may be determined by a target blood sugar, a carbohydrate-to-insulin ratio, a correction factor, and an insulin duration.
  • the current blood sugar value means a blood sugar value measured within 10 minutes.
  • the user may input the current blood glucose value 210 into the drug injection amount calculator.
  • the user may omit the input of the amount of carbohydrates consumed.
  • the user may input the current blood glucose value 210 in units of mg/dl.
  • the user may input 220 mg/dl as the current blood glucose value 210 .
  • the drug injection amount calculator may calculate 2.00U as the bolus injection amount 231 based on the current blood sugar value 210 .
  • a unit that can be input as the current blood glucose value 210 may be mmol/l, but is not limited to the above-described unit example.
  • the user may input the current blood sugar value 210 and the intake amount of carbohydrate 220 into the drug injection amount calculator.
  • the user may input the current blood sugar value 210 in mg/dl unit and may input the intake carbohydrate amount 220 in g unit.
  • the user may input 220 mg/dl as the current blood sugar value 210 and input 20 g as the intake carbohydrate amount 220 .
  • the drug injection amount calculator may calculate 1.30U as the bolus injection amount 232 based on the current blood glucose value 210 and the intake carbohydrate amount 220 .
  • FIG. 3 is a diagram illustrating an internal configuration of a drug injection device according to an embodiment.
  • the drug injection device 1 may include a housing 5 covering the outside, and an attachment part 6 attached to the user's skin.
  • the drug injection device 1 has a plurality of parts disposed in the inner space between the housing 5 and the attachment part 6 .
  • the drug injection device 1 includes a base body 50, a needle assembly 100, a storage unit 201, a driving unit 300, a driving unit 400, a clutch unit 500, a trigger member 600, and a battery ( 700) may be included.
  • the base body 50 forms a basic frame of the housing 5 , and is mounted in the inner space of the housing 5 .
  • the base body 50 may be provided in plurality.
  • a first body 50a that covers upper sides of the internal parts and a second body 50b that covers lower sides of the internal parts may be provided.
  • the first body 50a and the second body 50b may be assembled to fix the internal parts of the drug injection device 1 to a preset position.
  • the base body may be formed as an integral single frame.
  • the storage unit 201 is mounted on the base body 50 and is fluidly connected to the needle assembly 100 . Inside the storage unit 201, a plunger (not shown) moves linearly, so that the drug can be discharged with the needle (N).
  • the driving unit 300 may generate a driving force and transmit the driving force to the driving unit 400 .
  • the driving force transmitted by the driving unit 400 may linearly move the plunger 230 inside the storage unit 201 to discharge the drug.
  • the driving unit 300 may be any type of pump having a drug suction power and a drug discharge power by electricity.
  • pumps such as mechanical displacement type micropumps and electromagnetic motion type micropumps can be used.
  • a mechanical displacement micropump is a pump that uses the motion of a solid or fluid, such as a gear or diagram, to generate a pressure difference to induce the flow of a fluid.
  • Electromagnetic motion micropumps are pumps that directly use electrical or magnetic energy to move a fluid.
  • the driving unit 300 rotates the driving wheel of the driving unit 400 , and the rod moves linearly with the rotation of the driving wheel, so that a plunger (not shown) ) may be moved inside the storage unit 201 .
  • the driving unit 300 may include a membrane 320 disposed inside the cover 310 .
  • the membrane 320 may divide the inner space of the driving unit 300 into a first space S1 and a second space S2 .
  • the driving unit 300 may linearly move the driving shaft 330 by a volume change of the first space S1 and the second space S2 .
  • FIG. 4 is a view for explaining an example of providing a notification according to the period of use of the drug injection device according to an embodiment.
  • the drug injection device is maintained in an inactive mode before use, and may be switched from an inactive mode to an active mode by a predetermined operation.
  • In the inactive mode of the drug injection device power may not be supplied to at least some components inside the drug injection device.
  • the active mode of the drug infusion device power may be supplied to configurations that were not powered in the inactive mode.
  • power may not be supplied to the driving unit 300 of the drug injection device 1 in the inactive mode.
  • the driving force of the driving unit 300 is required.
  • the inactive mode power is not supplied to the driving unit 300, so the drug stored in the storage unit 201 is not injected to the user.
  • the active mode as power is supplied to the driving unit 300 of the drug injection device 1 , the drug stored in the storage unit 201 may be injected to the user.
  • the predetermined operation of switching the drug injection device 1 from the inactive mode to the active mode may be a drug replenishment operation.
  • the drug injection device 1 may further include a sensor unit for detecting drug replenishment in the storage unit 201 .
  • the plunger connected to the cover of the storage unit 201 may move linearly.
  • a connector member is attached to one side of the plunger, and the connector member moves together with the plunger and may contact at least a portion of the sensor unit.
  • the drug injection device 1 may be switched from the inactive mode to the active mode.
  • the method of switching the drug injection device 1 from the inactive mode to the active mode is not limited thereto.
  • a use start time 410 represents a time point at which the drug injection device is switched from an inactive mode to an active mode. For example, a point in time when one end of the connector member contacts at least a portion of the sensor unit may be the start point of use 410 . For example, when 80 Units or more of drugs are injected from the drug injection device to the patient, the drug injection device may be switched from the inactive mode to the active mode.
  • the controller transmits and receives data to and from the drug injection device and may control the drug injection device.
  • the controller determines that the expiration of the use period of the drug injection device is imminent at the first time point 420 after a predetermined period has passed from the start time point 410 of use. Notifications can be provided.
  • the first time point 420 may be set to any time from 1 hour to 24 hours before the time when the expiration notification is provided.
  • the controller may provide an expiration notification indicating that the use period of the drug injection device has expired at a second time point 430 after the usable period has passed from the use start time 410 .
  • the usable period of the drug injection device is, while the drug is injected from the drug injection device to the user, the material of the object that is kept inserted into the user's body and the material coated on the material (eg, membrane, etc.) may be determined based on at least one of.
  • the usable period of the drug injection device may be determined based on the structure of the object maintained in a state of being inserted into the user's body while the drug is injected from the drug injection device to the user. That is, the usable period of the drug injection device may be determined according to how long the object can be maintained while being inserted into the user's body.
  • the drug injection device 1 is attached to the user.
  • the user attaches the drug injection device 1 to the user, rotates the needle assembly 100, and inserts the needle N and the cannula into the skin.
  • the needle N is inserted into the skin together with the cannula, and may induce the cannula to be inserted into the skin.
  • the needle (N) is withdrawn from the skin, maintaining a state connected to the cannula.
  • the needle N moves upward while the cannula is inserted into the skin. At least a part of the cannula and the needle (N) is connected, and forms and maintains a path through which the drug solution moves.
  • the cannula is maintained in a state inserted into the user's body, and the drug stored in the storage unit 201 may be injected to the user through the cannula.
  • the usable period of the drug injection device may be determined based on the material of the cannula. Depending on the material of the cannula, the period for which safety is ensured when the cannula is maintained in a state of being inserted into the human body may vary.
  • the material of the cannula may include Teflon, and in this case, the usable period of the drug injection device may be set to 3.5 days.
  • the controller may provide an expiration notification indicating that the use period of the drug injection device has expired.
  • Teflon when other materials as well as Teflon are included as the material of the cannula, or when a material other than Teflon is included, the usable period may be set differently.
  • the user may be provided with an imminent expiration notification by setting an arbitrary time before the usable period of the drug injection device has elapsed. For example, if the usable period of the drug injection device is set to 3.5 days (84 hours), and the user set time is 1 hour, 83 hours (84 hours - 1 hour) have elapsed from the start time 410 of use. At one time point 420 , the controller may provide an imminent expiration notification indicating that the expiration date of the use period of the drug injection device is imminent.
  • the usable period of the drug injection device has been described as being determined based on the material of the cannula, but with the needle (N) inserted into the body If maintained, the usable period of the drug injection device may be determined based on the material of the needle (N).
  • the usable period of the drug injection device may be determined based on the storage capacity and the average daily dose.
  • the storage capacity and the average daily dose may be expressed in units of units.
  • the unit unit may mean a minimum unit when the drug stored in the storage unit is injected into the human body by the driving unit pump.
  • the average daily dose may be an average daily dose calculated by the dose statistics of a plurality of patients, rather than the average daily dose for each individual patient.
  • the average daily dose may vary depending on the number of type diabetes patients calculated by the dose statistics. For example, the average daily dose of patients with type 2 diabetes may be set to be higher than the average daily dose of patients with type 1 diabetes.
  • the average daily dose may vary depending on the concentration of the drug stored in the drug injection device. For example, when a drug containing 100Unit in 1ml is administered to a patient, and when a drug containing 200Unit or 500Unit in 1ml is administered to a patient, the average daily dose may be set differently.
  • the controller may provide an expiration notification indicating that the use period of the drug injection device has expired.
  • the user may be provided with an imminent expiration notification before the usable period is reached. For example, if the usable period of the drug injection device is set to 3.5 days (84 hours), and the user set time is 1 hour, 83 hours (84 hours - 1 hour) have elapsed from the start time 410 of use. At one time point 420 , the controller may provide an imminent expiration notification indicating that the expiration date of the use period of the drug injection device is imminent.
  • the usable period of the drug injection device may vary.
  • the usable period of the drug injection device is the material of the object that remains inserted into the user's body while the drug is injected from the drug injection device to the user, the material coated on the material, and the structure of the object It may be determined based on at least one of, the storage capacity and the average daily dose.
  • the controller compares the first period in which safety is ensured when the cannula is maintained in a state inserted into the human body and the second period calculated based on the storage capacity and the average daily dose of the drug injection device. You can decide how long you can use it.
  • the second period The second time point 430 may be set to 3 days, which is the shorter period of the first period (4 days) and the second period (3 days).
  • the second time point 430 may be set to 3.5 days, which is a shorter period of the first period (3.5 days) and the second period (4 days).
  • the controller adjusts the usable period of the drug injection device in consideration of the change. can be updated.
  • the controller may provide an imminent expiration notification and an expiration notification via the drug infusion device.
  • the controller may directly provide an imminent expiration notification and an expiration notification.
  • the controller may transmit data to the user terminal and provide an imminent expiration notification and an expiration notification from the user terminal.
  • 5 is a view for explaining an example of providing a notification according to the period of use of the drug injection device according to an embodiment.
  • a timeline to which a third viewpoint 550 and a fourth viewpoint 540 are further added is shown.
  • the drug injection device may further include a service period in addition to the usable period.
  • the drug infusion device may operate in an active mode during the usable period and the service period. That is, even if the usable period has elapsed, the drug injection device may operate normally if the service period does not elapse.
  • the usable period may be a period known to the user through the manuals, whereas the service period may be a period unknown to the user.
  • the drug injection device operates normally in the active mode even during the service period and injects the drug to the user, so that the user can receive the drug from the drug injection device for a certain period even when the usable period expires.
  • the controller based on the usable period of the drug injection device, the service period, and the user set time, discards that the drug injection device is about to be discarded at a fourth time point 540 after a predetermined period has passed from the use start time 510 .
  • An imminent notification can be provided.
  • the fourth time point 540 is a time point before the usable period and the service period elapse from the use start time 510 .
  • the controller may provide a discard notification indicating that the drug injection device should be discarded at a third time point 550 after the usable period and service period from the start of use 510 .
  • the third time point 550 may be a time when 12 hours have passed since the second time point 540 .
  • the usable period and service period of the drug injection device are, while the drug is injected from the drug injection device to the user, the material of the object that remains inserted into the user's body, the material coated on the material, and the It may be determined based on at least one of the structures of the object.
  • the usable period and service period of the drug injection device may be determined based on the material of the cannula. Depending on the material of the cannula, the period for which safety is guaranteed when the cannula is maintained in the human body may vary, so the usable period and service period of the drug injection device may be set differently depending on the material of the cannula .
  • the material of the cannula may include Teflon, and in this case, the usable period and service period of the drug injection device may be set to 4 days.
  • the controller may provide a discard notification indicating that the drug injection device should be discarded.
  • the usable period may be set differently.
  • the user may be provided with an imminent disposal notification by setting an arbitrary time before the expiration of the service period after the expiration of the usable period of the drug injection device.
  • the usable period and service period of the drug injection device are set to 4 days (96 hours), and when the user set time is 1 hour, 95 hours (96 hours - 1 hour) from the start of use 510
  • the controller may provide an imminent disposal notification indicating that the expiry of the period indicating that the drug injection device is imminent is imminent.
  • the usable period and service period of the drug injection device may be determined based on the storage capacity and the average daily dose.
  • the controller may provide a discard notification indicating that the drug injection device should be discarded.
  • the user may be provided with an imminent disposal notification by setting an arbitrary time before the expiration of the service period after the expiration of the usable period of the drug injection device.
  • the usable period and service period of the drug injection device are set to 4 days (96 hours), and when the user set time is 1 hour, 96 hours (96 hours - 1 hour) from the start time of use 510
  • the controller may provide an imminent disposal notification indicating that the disposal of the drug injection device is imminent.
  • the usable period and service period of the drug injection device include the material of the object that remains inserted into the user's body while the drug is injected from the drug injection device to the user, the material coated on the material, and the It may be determined based on at least one of the subject's structures, the storage capacity, and the average daily dose.
  • the controller compares the first period in which safety is ensured when the cannula is kept inserted into the human body and the second period calculated based on the storage capacity and the average daily dose to use the drug injection device. It is possible to determine the available period and service period.
  • the second period The three time points 550 may be set to 3 days, which is the shorter period of the first period (4 days) and the second period (3 days).
  • the third time point 550 may be set to 3.5 days, which is a shorter period of the first period (3.5 days) and the second period (4 days).
  • a first time point 520 indicating that the use period of the drug injection device is about to expire and a second time point 530 for providing an expiration notification indicating that the use of the drug injection device has expired may be arbitrarily set.
  • the third time point 550 is set to 4 days (96 hours) after the use start time 510 has elapsed
  • the second time point 530 is 3.5 days (84 hours) from the use start time 510 .
  • the first time point 520 may be set after 83 hours have elapsed from the use start time point 510 .
  • the usable period of the drug infusion device is determined based on the storage capacity and the average daily dose, and the total period of the drug infusion device plus the service period is the drug from the drug infusion device to the user. This may be determined based on at least one of a material of the object maintained in a state inserted into the user's body during the injection, a material coated on the material, and a structure of the object.
  • the controller may determine a first period for which safety is ensured when the cannula is maintained in the human body as the total period, and use the second period calculated based on the storage capacity and the average daily dose period can be determined.
  • the second period The third time point 550 may be set as a first period of 4 days, and the second time point 530 may be set as a second period of 3 days.
  • Methods of providing an imminent expiration notification, an expiration notification, an imminent retirement notification, and a retirement notification may be different from each other.
  • the vibration cycle, vibration intensity, LED color display, LED blinking cycle, and notification repeat cycle of each notification may be different from each other. The user can easily determine whether the notification corresponds to an imminent expiration notification, an expiration notification, an imminent retirement notification, or a retirement notification only by the manner in which the notification is provided.
  • FIG. 6 is a flowchart of a method of providing a notification according to the period of use of the drug injection device according to an embodiment.
  • the controller may communicate with the drug injection device.
  • the controller may be a component included in a user terminal such as a smart phone or a PC, or may be a component independent of the user terminal.
  • the controller may be a component included in the drug injection device.
  • the drug injection device and the controller perform communication using a network.
  • the controller may determine a time when the drug injection device is switched from the inactive mode to the active mode as the start time of use.
  • the drug injection device may be switched from an inactive mode to an active mode by a predetermined operation.
  • the predetermined operation may be a drug replenishment operation.
  • one end of the connector member connected to the plunger may be in contact with at least a portion of the sensor unit while the plunger connected to the cover of the reservoir moves linearly.
  • the drug injection device may be switched from the inactive mode to the active mode.
  • the drug injection device may transmit an active mode switching signal to the controller.
  • the controller may determine the time when the active mode switching signal is received from the drug injection device as the start time of use.
  • a communication network between the controller and the drug injection device may not be formed.
  • the drug injection device may be switched to the active mode with the controller to transmit elapsed time information.
  • step 620 the controller provides an expiration imminent notification indicating that the expiration date of the drug injection device is imminent at a first time point when a predetermined period has passed from the start of use, based on the usable period of the drug injection device and the user set time can do.
  • the controller may provide an expiration notification indicating that the use period of the drug injection device has expired at a second time point when the usable period has passed from the start of use.
  • the usable period of the drug injection device may be determined based on the material of the object maintained in the user's body while the drug is injected from the drug injection device to the user. In another embodiment, the usable period of the drug injection device may be determined based on the storage capacity and the average daily dose. In another embodiment, the usable period of the drug injection device is based on the material of the subject, the storage capacity, and the average daily dose of the subject that remains inserted into the user's body while the drug is injected from the drug injection device to the user. can be decided.
  • the drug injection device may further include a service period in addition to the usable period.
  • the drug infusion device may operate in an active mode during the usable period and the service period. That is, even if the usable period has elapsed, the drug injection device may operate normally if the service period does not elapse.
  • the controller controls the drug at a fourth time point after a predetermined period from the start of use based on the usable period, service period, and user set time of the drug injection device.
  • An imminent disposal notification may be provided that the disposition of the injection device is imminent.
  • the fourth time point is a time point before the usable period and service period elapse from the use start time 510 .
  • the controller may provide a discard notification that the drug injection device should be discarded at a third time point after the usable period and the service period from the start of use.
  • the usable period and service period of the drug injection device may be determined based on the material of the object that is maintained in a state inserted into the user's body while the drug is injected from the drug injection device to the user. In another embodiment, the usable period and service period of the drug injection device may be determined based on the storage capacity and the average daily dose. In another embodiment, the usable period of the drug injection device is based on the material of the subject, the storage capacity, and the average daily dose of the subject that remains inserted into the user's body while the drug is injected from the drug injection device to the user. can be decided.
  • the drug injection device further includes a service period in addition to the usable period, the first time point indicating that the usage period of the drug injection device is imminent and the second time point for providing an expiration notification indicating that the use of the drug injection device has expired are arbitrarily can be set.
  • Various embodiments of the present disclosure may be implemented as software (eg, a program) including one or more instructions stored in a storage medium readable by a machine.
  • the processor of the device may call at least one of the one or more instructions stored from the storage medium and execute it. This makes it possible for the device to be operated to perform at least one function according to the called at least one command.
  • the one or more instructions may include code generated by a compiler or code executable by an interpreter.
  • the device-readable storage medium may be provided in the form of a non-transitory storage medium.
  • 'non-transitory' only means that the storage medium is a tangible device and does not contain a signal (eg, electromagnetic wave), and this term is used in cases where data is semi-permanently stored in the storage medium and It does not distinguish between temporary storage cases.
  • a signal eg, electromagnetic wave
  • the method according to various embodiments of the present disclosure may be provided by being included in a computer program product.
  • Computer program products can be traded between sellers and buyers as commodities.
  • Computer programs products are distributed in the form of a device-readable storage medium (eg compact disc read only memory (CD-ROM)), or through an application store (eg Play StoreTM) or between two user devices. It can be distributed directly or online (eg, downloaded or uploaded).
  • a device-readable storage medium eg compact disc read only memory (CD-ROM)
  • an application store eg Play StoreTM
  • It can be distributed directly or online (eg, downloaded or uploaded).
  • online distribution at least a part of a computer, a program, and a product may be temporarily stored or temporarily created in a machine-readable storage medium such as a server of a manufacturer, a server of an application store, or a memory of a relay server.
  • unit may be a hardware component such as a processor or circuit, and/or a software component executed by a hardware component such as a processor.

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Abstract

The present invention may provide a method, a device, and a computer program product for providing a notification according to the period of use of a medicine injection device. In the present invention, it is possible to determine that a time point at which the medicine injection device switches from an inactive mode to an active mode is a use start time point. Furthermore, it is possible to provide, on the basis of the usable period of the medicine injection device and a user setting time, an expiration-imminent notification indicating that the expiration of use period of the medicine injection device is imminent, at a first time point at which a predetermined period has elapsed from the use start time point. Furthermore, it is possible to provide an expiration notification indicating that the use period of the medicine injection device has expired, at a second time point at which the usable period has elapsed from the use start time point.

Description

약물 주입 장치의 사용 기간에 따른 알림을 제공하는 방법, 장치 및 컴퓨터 프로그램 제품Methods, devices and computer program products for providing reminders based on age of drug infusion devices
본 개시는 약물 주입 장치의 사용 기간에 따른 알림을 제공하는 방법, 장치 및 컴퓨터 프로그램 제품을 제공한다.The present disclosure provides a method, an apparatus, and a computer program product for providing a notification according to the period of use of a drug injection device.
당뇨병은 인슐린의 분비량이 부족하거나 정상적인 기능이 이루어지지 않아 혈당이 정상 범위를 벗어나는 징후를 일으키는 대사 장애이다. 당뇨병은 실명, 신부전, 심부전, 신경병증 등의 합병증으로 인해 인체 각 조직에 영향을 미칠 가능성이 있는 복합병이며, 당뇨병 환자 수는 매년 증가하고 있다고 한다. Diabetes mellitus is a metabolic disorder that causes signs that blood sugar is outside the normal range due to insufficient insulin secretion or normal function. Diabetes mellitus is a complex disease that has the potential to affect individual tissues of the human body due to complications such as blindness, renal failure, heart failure, and neuropathy, and the number of diabetic patients is increasing every year.
당뇨병의 경우, 혈당측정기를 이용하여 혈당을 측정하고, 식이요법, 운동 프로그램, 인슐린 주사, 경구 당뇨약 등과 같은 적절한 수단을 통해 혈당을 관리할 필요가 있다.In the case of diabetes, it is necessary to measure blood sugar using a blood glucose meter, and to manage blood sugar through appropriate means such as diet, exercise program, insulin injection, oral diabetes medication, and the like.
최근에는 당뇨병 환자에게 약물 주입 장치를 이용하여 자동으로 인슐린을 주입하는 기술이 연구되고 있으며, 약물 주입 장치의 사용 기간을 효과적으로 사용자에게 알릴 수 있는 기술이 요구되는 실정이다.Recently, a technology for automatically injecting insulin to a diabetic patient using a drug injection device has been studied, and a technology capable of effectively notifying a user of the period of use of the drug injection device is required.
본 발명은 약물 주입 장치의 사용 기간에 따른 알림을 제공하는 방법, 장치 및 컴퓨터 프로그램 제품을 제공하는데 있다. 본 실시예가 이루고자 하는 기술적 과제는 상기된 바와 같은 기술적 과제들로 한정되지 않으며, 이하의 실시예들로부터 또 다른 기술적 과제들이 유추될 수 있다.An object of the present invention is to provide a method, an apparatus and a computer program product for providing a notification according to the period of use of a drug injection device. The technical problem to be achieved by this embodiment is not limited to the technical problems as described above, and other technical problems may be inferred from the following embodiments.
상술한 기술적 과제를 달성하기 위한 기술적 수단으로서, 본 개시의 제1 측면은, 약물 주입 장치의 사용 기간에 따른 알림을 제공하는 방법에 있어서, 약물 주입 장치가 비활성 모드(inactive mode)에서 활성 모드(active mode)로 전환되는 시점을 사용 개시 시점으로 결정하는 단계; 상기 약물 주입 장치의 사용 가능 기간 및 사용자 설정 시간에 기초하여, 상기 사용 개시 시점으로부터 소정의 기간이 지난 제1 시점 에 상기 약물 주입 장치의 사용 기간 만료가 임박하였다는 만료 임박 알림을 제공하는 단계; 및 상기 사용 개시 시점으로부터 상기 사용 가능 기간이 지난 제2 시점 에 상기 약물 주입 장치의 사용 기간이 만료되었다는 만료 알림을 제공하는 단계;를 제공할 수 있다.As a technical means for achieving the above-described technical problem, a first aspect of the present disclosure is a method for providing a notification according to the period of use of a drug injection device, wherein the drug injection device is operated in an inactive mode in an active mode ( determining the time to switch to active mode) as the time to start using; based on the usable period of the drug injection device and a user-set time, providing an imminent expiration notification indicating that the expiration date of the use period of the drug injection device is imminent at a first time point when a predetermined period has elapsed from the start of use; and providing an expiration notice indicating that the use period of the drug injection device has expired at a second time point when the usable period has elapsed from the start of use.
본 개시의 제 2 측면은, 약물 주입 장치의 사용 기간에 따른 알림을 제공하는 장치에 있어서, 적어도 하나의 프로그램이 저장된 메모리; 및 상기 적어도 하나의 프로그램을 실행함으로써 연산을 수행하는 프로세서를 포함하고, 상기 프로세서는, 약물 주입 장치가 비활성 모드에서 활성 모드로 전환되는 시점을 사용 개시 시점으로 결정하고, 상기 약물 주입 장치의 사용 가능 기간 및 사용자 설정 시간에 기초하여, 상기 사용 개시 시점으로부터 소정의 기간이 지난 제1 시점에 상기 약물 주입 장치의 사용 기간 만료가 임박하였다는 만료 임박 알림을 제공하고, 상기 사용 개시 시점으로부터 상기 사용 가능 기간이 지난 제2 시점에 상기 약물 주입 장치의 사용 기간이 만료되었다는 만료 알림을 제공하는 것인, 장치를 제공할 수 있다.A second aspect of the present disclosure provides an apparatus for providing a notification according to a period of use of a drug injection device, comprising: a memory in which at least one program is stored; and a processor that performs an operation by executing the at least one program, wherein the processor determines a time when the drug injection device is switched from an inactive mode to an active mode as a use start time, and the drug injection device can be used Based on a period and a user set time, an imminent expiration notification indicating that the expiration of the use period of the drug injection device is imminent is provided at a first time point when a predetermined period has elapsed from the start of use, and the use is possible from the start of use A device may be provided that provides an expiration notification indicating that the period of use of the drug injection device has expired at a second time point when the period has elapsed.
본 개시의 제 3 측면은, 약물 주입 장치가 비활성 모드(inactive mode)에서 활성 모드(active mode)로 전환되는 시점을 사용 개시 시점으로 결정하는 단계; 상기 약물 주입 장치의 사용 가능 기간 및 사용자 설정 시간에 기초하여, 상기 사용 개시 시점으로부터 소정의 기간이 지난 제1 시점에 상기 약물 주입 장치의 교체 임박 알림을 제공하는 단계; 및 상기 사용 개시 시점으로부터 상기 사용 가능 기간이 지난 제2 시점에 상기 약물 주입 장치의 사용 기간이 만료되었다는 만료 알림을 제공하는 단계;를 수행하도록 하는 프로그램이 저장된 하나 이상의 컴퓨터로 읽을 수 있는 기록매체를 포함하는 컴퓨터 프로그램 제품을 제공할 수 있다.A third aspect of the present disclosure includes the steps of: determining a time when the drug injection device is switched from an inactive mode to an active mode as a start time of use; providing a notification of imminent replacement of the drug injection device at a first time point when a predetermined period has elapsed from the start time of use, based on a usable period of the drug injection device and a user-set time; and providing an expiration notification that the use period of the drug injection device has expired at a second time point when the usable period has passed from the start of use; one or more computer-readable recording media storing a program to perform A computer program product comprising the may be provided.
전술한 본 개시의 과제 해결 수단에 의하면, 약물 주입 장치의 저장부 용량 및 하루 평균 투여량에 기초하여 약물 주입 장치의 사용기간을 결정하고, 사용기간에 따른 알림을 제공함으로써, 사용의 편의성을 제공할 수 있다.According to the above-described problem solving means of the present disclosure, convenience of use is provided by determining the period of use of the drug injection device based on the storage capacity and the average daily dose of the drug injection device, and providing a notification according to the period of use can do.
본 개시의 다른 과제 해결 수단 중 하나에 의하면, 약물 주입 장치로부터 사용자에게 약물이 주입되는 동안, 사용자 인체에 삽입된 상태로 유지되는 대상체의 소재에 기초하여 약물 주입 장치의 사용기간을 결정함으로써, 약물 주입 장치를 안전하게 사용하는 방법을 제공할 수 있다.According to one of the other problem solving means of the present disclosure, while the drug is injected from the drug injection device to the user, by determining the period of use of the drug injection device based on the material of the object maintained in the state inserted into the user's body, the drug A method for safely using an injection device may be provided.
도 1은 사용자 단말, 컨트롤러 및 약물 주입 장치를 포함하는 인슐린 관리 시스템의 블록도이다.1 is a block diagram of an insulin management system including a user terminal, a controller, and a drug injection device.
도 2a 내지 도 2b는 일 실시예에 따른 약물 주입량 계산기의 설정 방법을 설명하기 위한 예시적인 도면이다.2A to 2B are exemplary views for explaining a method of setting a drug injection amount calculator according to an embodiment.
도 3은 일 실시예에 따른 약물 주입 장치의 내부 구성을 도시한 도면이다.3 is a diagram illustrating an internal configuration of a drug injection device according to an embodiment.
도 4는 일 실시예에 따른 약물 주입 장치의 사용 기간에 따른 알림을 제공하는 예시를 설명하기 위한 도면이다.4 is a view for explaining an example of providing a notification according to the period of use of the drug injection device according to an embodiment.
도 5는 일 실시예에 따른 약물 주입 장치의 사용 기간에 따른 알림을 제공하는 예시를 설명하기 위한 도면이다.5 is a view for explaining an example of providing a notification according to the period of use of the drug injection device according to an embodiment.
도 6은 일 실시예에 따른 약물 주입 장치의 사용 기간에 따른 알림을 제공하는 방법의 흐름도이다.6 is a flowchart of a method of providing a notification according to the period of use of the drug injection device according to an embodiment.
약물 주입 장치의 사용 기간에 따른 알림을 제공하는 방법, 장치 및 컴퓨터 프로그램 제품을 제공할 수 있다.It is possible to provide a method, an apparatus, and a computer program product for providing a notification according to the period of use of the drug injection device.
본 발명에서는, 약물 주입 장치가 비활성 모드(inactive mode)에서 활성 모드(active mode)로 전환되는 시점을 사용 개시 시점으로 결정할 수 있다. 또한, 약물 주입 장치의 사용 가능 기간 및 사용자 설정 시간에 기초하여, 사용 개시 시점으로부터 소정의 기간이 지난 제1 시점에 약물 주입 장치의 사용 기간 만료가 임박하였다는 만료 임박 알림을 제공할 수 있다. 또한, 사용 개시 시점으로부터 사용 가능 기간이 지난 제2 시점에 약물 주입 장치의 사용 기간이 만료되었다는 만료 알림을 제공할 수 있다.In the present invention, a time when the drug injection device is switched from an inactive mode to an active mode may be determined as a start time of use. In addition, based on the usable period of the drug injection device and the user-set time, an imminent expiration notification indicating that the expiration of the use period of the drug injection device is imminent may be provided at a first time point after a predetermined period from the start of use. In addition, an expiration notification indicating that the use period of the drug injection device has expired may be provided at a second time point when the usable period has elapsed from the start of use.
아래에서는 첨부한 도면을 참조하여 본 발명이 속하는 기술 분야에서 통상의 지식을 가진 자가 용이하게 실시할 수 있도록 본 발명의 실시예를 상세히 설명한다. 그러나 본 발명은 여러 가지 상이한 형태로 구현될 수 있으며 여기에서 설명하는 실시예에 한정되지 않는다. 그리고 도면에서 본 발명을 명확하게 설명하기 위해서 설명과 관계없는 부분은 생략하였으며, 명세서 전체를 통하여 유사한 부분에 대해서는 유사한 도면 부호를 붙였다. DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS Hereinafter, embodiments of the present invention will be described in detail with reference to the accompanying drawings so that those of ordinary skill in the art can easily implement them. However, the present invention may be embodied in several different forms and is not limited to the embodiments described herein. And in order to clearly explain the present invention in the drawings, parts irrelevant to the description are omitted, and similar reference numerals are attached to similar parts throughout the specification.
명세서 전체에서, 어떤 부분이 다른 부분과 "연결"되어 있다고 할 때, 이는 "직접적으로 연결"되어 있는 경우뿐 아니라, 그 중간에 다른 소자를 사이에 두고 "전기적으로 연결"되어 있는 경우도 포함한다. 또한 어떤 부분이 어떤 구성요소를 "포함"한다고 할 때, 이는 특별히 반대되는 기재가 없는 한 다른 구성요소를 제외하는 것이 아니라 다른 구성요소를 더 포함할 수 있는 것을 의미한다.Throughout the specification, when a part is "connected" with another part, this includes not only the case of being "directly connected" but also the case of being "electrically connected" with another element interposed therebetween. . Also, when a part "includes" a certain component, it means that other components may be further included, rather than excluding other components, unless otherwise stated.
이하 첨부된 도면을 참고하여 본 개시를 상세히 설명하기로 한다.Hereinafter, the present disclosure will be described in detail with reference to the accompanying drawings.
도 1은 사용자 단말, 컨트롤러 및 약물 주입 장치를 포함하는 인슐린 관리 시스템의 블록도이다. 1 is a block diagram of an insulin management system including a user terminal, a controller, and a drug injection device.
사용자 단말(1000)은 유무선 통신 환경에서 웹 서비스를 이용할 수 있는 통신 단말을 의미한다. 예를 들어, 사용자 단말(1000)은 스마트폰, 태블릿 PC, PC, 스마트 TV, 휴대폰, PDA(personal digital assistant), 랩톱, 미디어 플레이어, 마이크로 서버, GPS(global positioning system) 장치, 전자책 단말기, 디지털방송용 단말기, 네비게이션, 키오스크, MP3 플레이어, 디지털 카메라, 가전기기, 카메라가 탑재된 디바이스 및 기타 모바일 또는 비모바일 컴퓨팅 장치일 수 있다. 또한, 사용자 단말(1000)은 통신 기능 및 데이터 프로세싱 기능을 구비한 시계, 안경, 헤어 밴드 및 반지 등의 웨어러블 디바이스일 수 있다. 그러나, 상술한 바와 같이 인터넷 통신이 가능한 애플리케이션을 탑재한 단말은 제한 없이 차용될 수 있다. The user terminal 1000 refers to a communication terminal capable of using a web service in a wired/wireless communication environment. For example, the user terminal 1000 may include a smartphone, a tablet PC, a PC, a smart TV, a mobile phone, a personal digital assistant (PDA), a laptop, a media player, a micro server, a global positioning system (GPS) device, an e-book terminal, It may be a terminal for digital broadcasting, a navigation system, a kiosk, an MP3 player, a digital camera, a home appliance, a device equipped with a camera, and other mobile or non-mobile computing devices. Also, the user terminal 1000 may be a wearable device such as a watch, glasses, a hair band, and a ring having a communication function and a data processing function. However, as described above, a terminal equipped with an application capable of Internet communication may be borrowed without limitation.
사용자 단말(1000)은 미리 등록된 컨트롤러(2000)와 1대1로 연결될 수 있다. 또한, 사용자 단말들(1000)은 외부의 장치로부터의 제어를 막기 위해서, 컨트롤러(2000)로부터 데이터를 수신할 수 있다. 사용자 단말(1000)은 기 설정된 범위 안에서 설정 정보, 예를 들어 시스템 시간 정보를 컨트롤러(2000)로 전달할 수 있다. The user terminal 1000 may be connected one-to-one with the pre-registered controller 2000 . Also, the user terminals 1000 may receive data from the controller 2000 in order to prevent control from an external device. The user terminal 1000 may transmit setting information, for example, system time information, to the controller 2000 within a preset range.
컨트롤러(2000)는 약물 주입 장치(3000)와 데이터를 송수신하는 기능을 수행하며, 약물 주입 장치(3000)로 인슐린 등의 약물의 주입과 관련된 제어 신호를 전송하고, 약물 주입 장치(3000)로부터 혈당 등의 생체값의 측정과 관련된 제어 신호를 수신 받을 수 있다. The controller 2000 performs a function of transmitting and receiving data to and from the drug injection device 3000 , and transmits a control signal related to injection of a drug such as insulin to the drug injection device 3000 , and blood glucose from the drug injection device 3000 . It is possible to receive a control signal related to the measurement of a biological value, such as.
컨트롤러(2000)는 약물 주입 장치(3000)로 사용자의 현 상태를 측정하라는 지시 요청을 전송하고, 지시 요청의 응답으로 약물 주입 장치(3000)로부터 측정 데이터를 수신 받을 수 있다. The controller 2000 may transmit an instruction request to measure the user's current state to the drug injection device 3000 , and receive measurement data from the drug injection device 3000 in response to the instruction request.
이때, 약물 주입 장치(3000)는 사용자의 혈당값, 혈압, 심박수 등의 생체값을 측정하는 기능을 수행하기도 하지만, 사용자에게 주입되어야 하는 인슐린, 글루카곤, 마취제, 진통제, 도파민, 성장 호르몬, 금연 보조제 등의 약물을 주입하는 기능을 수행하기도 한다.At this time, the drug injection device 3000 also performs a function of measuring the user's blood sugar value, blood pressure, heart rate, etc., but should be injected into the user insulin, glucagon, anesthetic, analgesic, dopamine, growth hormone, smoking cessation aid It also performs the function of injecting drugs, such as.
약물 주입 장치(3000)는 사용자에게 주기적으로 주입되어야 하는 물질을 보관하는 저장부를 더 포함할 수 있으며, 컨트롤러에 의해 발생된 주입 신호에 따라 주입되어야 하는 주입량이 저장부로부터 주입되도록 제어될 수 있다. The drug injection device 3000 may further include a storage unit for storing a substance to be periodically injected to the user, and an injection amount to be injected may be controlled to be injected from the storage unit according to an injection signal generated by the controller.
이때, 약물 주입 장치(3000)는 측정값 및 주입량 등의 정보를 컨트롤러(2000)에 전달할 수 있다. 선택적으로 약물 주입 장치(3000)는 장치 상태 메시지, 생체값 측정 메시지, 약물 주입 메시지 등을 컨트롤러(2000)로 전달할 수 있다. 예를 들어, 약물 주입 장치(3000)는 장치의 잔여 배터리 용량 정보, 장치의 부팅 성공 여부, 주입 성공 여부 등을 포함하는 장치 상태 메시지를 컨트롤러(2000)에 전달할 수 있다. 컨트롤러로 전달된 메시지들은 컨트롤러(2000)를 거쳐 사용자 단말(1000)로 전달될 수 있다. 또는 컨트롤러(2000)는 수신된 메시지들을 가공한 개량 데이터를 사용자 단말(1000)로 전달할 수 있다. In this case, the drug injection device 3000 may transmit information such as a measurement value and an injection amount to the controller 2000 . Optionally, the drug injection device 3000 may transmit a device status message, a biometric value measurement message, a drug injection message, and the like to the controller 2000 . For example, the drug injection device 3000 may transmit a device status message including information on the remaining battery capacity of the device, whether the device is booted successfully, whether the injection is successful, and the like to the controller 2000 . Messages transmitted to the controller may be transmitted to the user terminal 1000 via the controller 2000 . Alternatively, the controller 2000 may transmit improved data obtained by processing the received messages to the user terminal 1000 .
약물 주입 장치(3000) 역시 미리 등록된 컨트롤러와만 통신가능하도록 구현될 수 있다. 또한, 약물 주입 장치(3000)는 하드웨어적으로, 사용자의 혈당값, 혈압, 심박수 등의 생체값을 측정하는 기능을 수행하는 측정 장치와, 인슐린, 글루카곤, 마취제, 등의 약물을 주입하는 기능을 수행하는 주입 장치로 구분될 수 있다. 즉, 측정 장치와 주입 장치가 독립적으로 존재할 수도 있다. 컨트롤러(2000)는 주입 장치 및 측정 장치와 각각 연결되어 측정 장치를 통해 측정된 측정값을 기초로 주입 장치에 대한 제어 신호를 생성하여 제공할 수 있다.The drug injection device 3000 may also be implemented to communicate only with a pre-registered controller. In addition, the drug injection device 3000 includes a hardware measuring device that performs a function of measuring a user's blood sugar level, blood pressure, heart rate, etc., and a function of injecting drugs such as insulin, glucagon, anesthetic, etc. It can be divided into an injection device that performs. That is, the measuring device and the injection device may exist independently. The controller 2000 may be respectively connected to the injection device and the measurement device to generate and provide a control signal for the injection device based on a measurement value measured by the measurement device.
한편, 사용자 단말(1000), 컨트롤러(2000) 및 약물 주입 장치(3000)는 네트워크를 이용하여 통신을 수행할 수 있다. 예를 들어, 네트워크는 근거리 통신망(Local Area Network; LAN), 광역 통신망(Wide Area Network; WAN), 부가가치 통신망(Value Added Network; VAN), 이동 통신망(mobile radio communication network), 위성 통신망 및 이들의 상호 조합을 포함하며, 각 네트워크 구성 주체가 서로 원활하게 통신을 할 수 있도록 하는 포괄적인 의미의 데이터 통신망이며, 유선 인터넷, 무선 인터넷 및 모바일 무선 통신망을 포함할 수 있다. 또한, 무선 통신은 예를 들어, 무선 랜(Wi-Fi), 블루투스, 블루투스 저 에너지(Bluetooth low energy), 지그비, WFD(Wi-Fi Direct), UWB(ultra wideband), 적외선 통신(IrDA, infrared Data Association), NFC(Near Field Communication) 등이 있을 수 있으나, 이에 한정되는 것은 아니다.Meanwhile, the user terminal 1000 , the controller 2000 , and the drug injection device 3000 may perform communication using a network. For example, a network includes a local area network (LAN), a wide area network (WAN), a value added network (VAN), a mobile radio communication network, a satellite communication network, and their It is a data communication network in a comprehensive sense that includes a mutual combination and enables each network constituent entity to communicate smoothly with each other, and may include a wired Internet, a wireless Internet, and a mobile wireless communication network. In addition, wireless communication is, for example, wireless LAN (Wi-Fi), Bluetooth, Bluetooth low energy, Zigbee, WFD (Wi-Fi Direct), UWB (ultra wideband), infrared communication (IrDA, infrared Data Association), NFC (Near Field Communication), etc. may be there, but is not limited thereto.
도 2a 내지 도 2b는 일 실시예에 따른 약물 주입량 계산기의 설정 방법을 설명하기 위한 예시적인 도면이다.2A to 2B are exemplary views for explaining a method of setting a drug injection amount calculator according to an embodiment.
도 1의 사용자 단말(1000), 컨트롤러(2000) 또는 약물 주입 장치(3000)에는 약물 주입량 계산기가 탑재될 수 있다. 약물 주입량 계산기는 기초 주입과 별도로 사용자에게 주입 되어야 하는 인슐린 양을 계산하는 계산기일 수 있다. 예를 들어 약물 주입량 계산기는, 음식이나 간식 섭취 때문에 올라가는 혈당을 내리기 위해 필요한 인슐린 양을 계산할 수 있다. 또한, 약물 주입량 계산기는 높은 혈당을 정상 혈당 범위 내로 내리기 위해 필요한 인슐린 양을 계산할 수 있다.A drug injection amount calculator may be mounted on the user terminal 1000 , the controller 2000 , or the drug injection device 3000 of FIG. 1 . The drug injection amount calculator may be a calculator for calculating the amount of insulin to be injected to the user separately from the basal injection. A medication dose calculator, for example, can calculate the amount of insulin needed to lower blood sugar, which rises due to eating food or snacks. In addition, the drug injection amount calculator may calculate the amount of insulin required to bring the high blood sugar into the normal blood sugar range.
상술한 바와 같이, 인슐린 기초 주입과는 별도로, 음식 섭취 또는 높은 혈당을 내려야 할 때에 주입하는 인슐린을 볼루스(bolus)라고 칭할 수 있다. 약물 주입량 계산기는 볼루스 계산기로 칭할 수 있고, 볼루스 계산기는 볼루스 주입량을 계산할 수 있다.As described above, apart from basal insulin injection, insulin injected when food intake or high blood sugar needs to be lowered may be referred to as a bolus. The drug injection amount calculator may be referred to as a bolus calculator, and the bolus calculator may calculate a bolus injection amount.
볼루스 주입량은 다양한 값들에 의해 결정될 수 있다. 예를 들어, 볼루스 주입량은, 현재 혈당 수치, 탄수화물 대 인슐린 비율, 교정 계수, 목표 혈당 수치, 이전 볼루스 주입량 중에 체내 활성화 시간이 남아있는 인슐린 양(Insulin On Board(IOB), Bolus on Board(BOB) 또는 Active Insulin), 교정 임계치, 활동량, 섭취한 음식의 종류와 양 등에 의해 결정될 수 있다. The bolus injection amount may be determined by various values. For example, the bolus injection amount is the current blood glucose level, carbohydrate-to-insulin ratio, correction factor, target blood glucose level, the amount of insulin remaining in body activation time during the previous bolus injection (Insulin On Board (IOB), Bolus on Board ( BOB) or Active Insulin), the correction threshold, the amount of activity, and the type and amount of food consumed.
교정 계수는 볼루스 인슐린 1Unit이 낮출 수 있는 혈당 수치를 나타낸 값입니다. 교정 계수의 범위는 1~400mg/dl/U이고, 1mg/dl/U씩 조절할 수 있다. 교정 임계치는 혈당 조절을 위해 인슐린 주입이 필요하다고 판단되는 혈당 최고치를 의미할 수 있다.The correction factor is a measure of the blood sugar level that 1Unit of bolus insulin can lower. The range of the correction factor is 1~400mg/dl/U, and it can be adjusted by 1mg/dl/U. The calibration threshold may mean a maximum blood sugar level at which it is determined that insulin injection is necessary for blood sugar control.
볼루스 계산기는 사용자 개인의 볼루스 프로필 설정 값, 현재 혈당값, 섭취한 탄수화물 양 및 체내 인슐린 잔량(IOB)에 기초하여 볼루스 주입량을 계산할 수 있다.The bolus calculator may calculate the bolus injection amount based on the user's individual bolus profile setting value, the current blood sugar value, the amount of carbohydrate consumed, and the remaining amount of insulin in the body (IOB).
구체적으로 볼루스 프로필 설정 값은, 목표 혈당, 탄수화물 대 인슐린 비율, 교정 계수, 인슐린 지속시간에 의해 결정될 수 잇다. 현재 혈당 값은 10분 이내 측정한 혈당 값을 의미한다.Specifically, the bolus profile setting value may be determined by a target blood sugar, a carbohydrate-to-insulin ratio, a correction factor, and an insulin duration. The current blood sugar value means a blood sugar value measured within 10 minutes.
도 2a를 참조하면, 사용자는 약물 주입량 계산기에 현재 혈당값(210)을 입력할 수 있다. 사용자는 섭취한 탄수화물 양에 대한 입력을 생략할 수 있다. 사용자는 mg/dl 단위로 현재 혈당값(210)을 입력할 수 있다. 예를 들어, 사용자는 현재 혈당값(210)으로 220mg/dl을 입력할 수 있다. 약물 주입량 계산기는 현재 혈당값(210)에 기초하여 볼루스 주입량(231)으로써 2.00U을 계산할 수 있다. 현재 혈당값(210)으로 입력될 수 있는 단위는 mmol/l일 수도 있으나, 상술한 단위 예시에 제한되지 않는다.Referring to FIG. 2A , the user may input the current blood glucose value 210 into the drug injection amount calculator. The user may omit the input of the amount of carbohydrates consumed. The user may input the current blood glucose value 210 in units of mg/dl. For example, the user may input 220 mg/dl as the current blood glucose value 210 . The drug injection amount calculator may calculate 2.00U as the bolus injection amount 231 based on the current blood sugar value 210 . A unit that can be input as the current blood glucose value 210 may be mmol/l, but is not limited to the above-described unit example.
도 2b를 참조하면, 사용자는 약물 주입량 계산기에 현재 혈당값(210) 및 섭취한 탄수화물 양(220)을 입력할 수 있다. 사용자는 mg/dl 단위로 현재 혈당값(210)을 입력할 수 있고, g 단위로 섭취한 탄수화물 양(220)을 입력할 수 있다. 예를 들어, 사용자는 현재 혈당값(210)으로 220mg/dl을 입력하고, 섭취한 탄수화물 양(220)으로 20g을 입력할 수 있다. 약물 주입량 계산기는 현재 혈당값(210) 및 섭취한 탄수화물 양(220)에 기초하여 볼루스 주입량(232)으로써 1.30U을 계산할 수 있다.Referring to FIG. 2B , the user may input the current blood sugar value 210 and the intake amount of carbohydrate 220 into the drug injection amount calculator. The user may input the current blood sugar value 210 in mg/dl unit and may input the intake carbohydrate amount 220 in g unit. For example, the user may input 220 mg/dl as the current blood sugar value 210 and input 20 g as the intake carbohydrate amount 220 . The drug injection amount calculator may calculate 1.30U as the bolus injection amount 232 based on the current blood glucose value 210 and the intake carbohydrate amount 220 .
도 3은 일 실시예에 따른 약물 주입 장치의 내부 구성을 도시한 도면이다.3 is a diagram illustrating an internal configuration of a drug injection device according to an embodiment.
도 3을 참조하면, 약물 주입 장치(1)는 외측을 커버하는 하우징(5), 사용자의 피부에 부착되는 부착부(6)를 구비할 수 있다. 약물 주입 장치(1)는 하우징(5)과 부착부(6) 사이의 내부 공간에 복수개의 부품이 배치된다. Referring to FIG. 3 , the drug injection device 1 may include a housing 5 covering the outside, and an attachment part 6 attached to the user's skin. The drug injection device 1 has a plurality of parts disposed in the inner space between the housing 5 and the attachment part 6 .
약물 주입 장치(1)는 베이스 바디(50), 니들 조립체(100), 저장부(201), 구동부(300), 구동 유닛(400), 클러치 유닛(500), 트리거 부재(600) 및 배터리(700)를 포함할 수 있다.The drug injection device 1 includes a base body 50, a needle assembly 100, a storage unit 201, a driving unit 300, a driving unit 400, a clutch unit 500, a trigger member 600, and a battery ( 700) may be included.
베이스 바디(50)는 하우징(5)의 기본적인 틀을 형성하며, 하우징(5)의 내부 공간에 장착된다. 베이스 바디(50)는 복수 개로 구비될 수 있다. 일 실시예로, 내부 부품들의 상측을 커버하는 제1 바디(50a)와, 내부 부품들의 하측을 커버하는 제2 바디(50b)를 구비할 수 있다. 제1 바디(50a)와 제2 바디(50b)는 조립되어, 약물 주입 장치(1)의 내부 부품을 기 설정 위치에 고정시킬 수 있다. 다른 실시예로, 베이스 바디는 일체형의 하나의 프레임으로 형성될 수 있다.The base body 50 forms a basic frame of the housing 5 , and is mounted in the inner space of the housing 5 . The base body 50 may be provided in plurality. In one embodiment, a first body 50a that covers upper sides of the internal parts and a second body 50b that covers lower sides of the internal parts may be provided. The first body 50a and the second body 50b may be assembled to fix the internal parts of the drug injection device 1 to a preset position. In another embodiment, the base body may be formed as an integral single frame.
저장부(201)는 베이스 바디(50)에 장착되며, 니들 조립체(100)와 유체적으로 연결된다. 저장부(201)의 내부에서는 플런저(미도시)가 선형 이동하여, 약물을 니들(N)로 배출할 수 있다.The storage unit 201 is mounted on the base body 50 and is fluidly connected to the needle assembly 100 . Inside the storage unit 201, a plunger (not shown) moves linearly, so that the drug can be discharged with the needle (N).
구동부(300)는 구동력을 생성하여 구동 유닛(400)에 구동력을 전달할 수 있다. 구동 유닛(400)에 의해 전달된 구동력은 플런저(230)를 저장부(201) 내부에 선형 이동시켜서, 약물을 배출할 수 있다. The driving unit 300 may generate a driving force and transmit the driving force to the driving unit 400 . The driving force transmitted by the driving unit 400 may linearly move the plunger 230 inside the storage unit 201 to discharge the drug.
구동부(300)는 전기에 의해 약물 흡입력과 약물 토출력을 갖는 모든 종류의 펌프가 사용될 수 있다. 예를 들면, 기계 변위형 마이크로펌프와 전자기운동형 마이크로펌프 등의 모든 종류의 펌프가 사용될 수 있다. 기계변위형 마이크로펌프는 유체의 흐름을 유도하기 위해 압력차를 일으키도록 기어나 다이어그램과 같은 고체 혹은 유체의 운동을 이용하는 펌프로서, 다이어프람 변위 펌프(Diaphragm displacement pump), 유체 변위 펌프(Fluid displacement pump), 회전 펌프(Rotary pump) 등이 있다. 전자기운동형 마이크로펌프는 전기적 또는 자기적 형태의 에너지를 바로 유체의 이동에 이용하는 펌프로서, 전기유체역학 펌프(Electro hydrodynamic pump, EHD), 전기삼투식 펌프(Electro osmotic pump), 자기유체역학 펌프(Magneto hydrodynamic pump), 전기습식 펌프(Electro wetting pump)등이 있다.The driving unit 300 may be any type of pump having a drug suction power and a drug discharge power by electricity. For example, all kinds of pumps such as mechanical displacement type micropumps and electromagnetic motion type micropumps can be used. A mechanical displacement micropump is a pump that uses the motion of a solid or fluid, such as a gear or diagram, to generate a pressure difference to induce the flow of a fluid. Diaphragm displacement pump, fluid displacement pump ), and a rotary pump. Electromagnetic motion micropumps are pumps that directly use electrical or magnetic energy to move a fluid. Electrohydrodynamic pumps (EHD), electroosmotic pumps, magnetohydrodynamic pumps ( Magneto hydrodynamic pump), electrowetting pump, etc.
구동부(300)는 클러치 유닛(500)에 의해서 구동 유닛(400)이 연결되면(engaged), 구동 유닛(400)의 구동 휠을 회전시키고, 구동 휠의 회전으로 로드가 선형 이동하여 플런저(미도시)가 저장부(201)의 내부에서 이동할 수 있다.When the driving unit 400 is engaged by the clutch unit 500 , the driving unit 300 rotates the driving wheel of the driving unit 400 , and the rod moves linearly with the rotation of the driving wheel, so that a plunger (not shown) ) may be moved inside the storage unit 201 .
구동부(300)는 커버(310)의 내부에 배치되는 멤브레인(320)을 구비할 수 있다. 멤브레인(320)은 구동부(300)의 내부 공간을 제1 공간(S1)과 제2 공간(S2)으로 구획할 수 있다. 구동부(300)는 제1 공간(S1)과 제2 공간(S2)의 체적 변화에 의해서 구동축(330)을 선형이동할 수 있다.The driving unit 300 may include a membrane 320 disposed inside the cover 310 . The membrane 320 may divide the inner space of the driving unit 300 into a first space S1 and a second space S2 . The driving unit 300 may linearly move the driving shaft 330 by a volume change of the first space S1 and the second space S2 .
도 4는 일 실시예에 따른 약물 주입 장치의 사용 기간에 따른 알림을 제공하는 예시를 설명하기 위한 도면이다.4 is a view for explaining an example of providing a notification according to the period of use of the drug injection device according to an embodiment.
약물 주입 장치는 사용 전 비활성 모드(inactive mode)에서 유지되고, 소정의 동작에 의해 비활성 모드에서 활성 모드(active mode)로 전환될 수 있다. 약물 주입 장치의 비활성 모드에서는, 약물 주입 장치 내부의 적어도 일부 구성에 전력이 공급되지 않을 수 있다. 약물 주입 장치의 활성 모드에서는, 비활성 모드에서 전력이 공급되지 않던 구성에 전력이 공급될 수 있다. The drug injection device is maintained in an inactive mode before use, and may be switched from an inactive mode to an active mode by a predetermined operation. In the inactive mode of the drug injection device, power may not be supplied to at least some components inside the drug injection device. In the active mode of the drug infusion device, power may be supplied to configurations that were not powered in the inactive mode.
도 3을 참조하여 설명하면, 일 실시예에서, 비활성 모드에서 약물 주입 장치(1)의 구동부(300)에는 전력이 공급되지 않을 수 있다. 저장부(201)에 저장된 약물을 배출하기 위해서는 구동부(300)의 구동력이 필요한데, 비활성 모드에서는 구동부(300)에 전력이 공급되지 않으므로 저장부(201)에 저장된 약물은 사용자에게 주입되지 않는다. 반면, 활성 모드에서는 약물 주입 장치(1)의 구동부(300)에 전력이 공급됨에 따라 저장부(201)에 저장된 약물이 사용자에게 주입될 수 있다.Referring to FIG. 3 , in one embodiment, power may not be supplied to the driving unit 300 of the drug injection device 1 in the inactive mode. In order to discharge the drug stored in the storage unit 201, the driving force of the driving unit 300 is required. In the inactive mode, power is not supplied to the driving unit 300, so the drug stored in the storage unit 201 is not injected to the user. On the other hand, in the active mode, as power is supplied to the driving unit 300 of the drug injection device 1 , the drug stored in the storage unit 201 may be injected to the user.
일 실시예에서, 약물 주입 장치(1)를 비활성 모드에서 활성 모드로 전환시키는 소정의 동작은 약물 보충 동작일 수 있다. 약물 주입 장치(1)는 저장부(201) 내 약물 보충을 감지하는 센서 유닛을 더 포함할 수 있다. 구체적으로, 저장부(201)에 약물이 보충됨에 따라 저장부(201)의 커버와 연결된 플런저가 선형 이동할 수 있다. 플런저의 일측에는 커넥터 부재가 부착되는데, 커넥터 부재는 플런저와 함께 이동하며 센서 유닛의 적어도 일부에 접촉할 수 있다. 커넥터 부재가 센서 유닛의 적어도 일부에 접촉한 경우, 약물 주입 장치(1)는 비활성 모드에서 활성 모드로 전환될 수 있다. 다만, 약물 주입 장치(1)가 비활성 모드에서 활성 모드로 전환되는 방법은 이에 제한되지 않는다.In one embodiment, the predetermined operation of switching the drug injection device 1 from the inactive mode to the active mode may be a drug replenishment operation. The drug injection device 1 may further include a sensor unit for detecting drug replenishment in the storage unit 201 . Specifically, as the drug is replenished in the storage unit 201 , the plunger connected to the cover of the storage unit 201 may move linearly. A connector member is attached to one side of the plunger, and the connector member moves together with the plunger and may contact at least a portion of the sensor unit. When the connector member contacts at least a part of the sensor unit, the drug injection device 1 may be switched from the inactive mode to the active mode. However, the method of switching the drug injection device 1 from the inactive mode to the active mode is not limited thereto.
도 4를 참조하면, 사용 개시 시점(410)은 약물 주입 장치는 비활성 모드에서 활성 모드로 전환되는 시점을 나타낸다. 예를 들어, 커넥터 부재의 일단부가 센서 유닛의 적어도 일부에 접촉한 시점이 사용 개시 시점(410)일 수 있다. 예를 들어, 약물 주입 장치로부터 환자에게 약물이 80Unit 이상 주입된 경우 약물 주입 장치는 비활성 모드에서 활성 모드로 전환될 수 있다.Referring to FIG. 4 , a use start time 410 represents a time point at which the drug injection device is switched from an inactive mode to an active mode. For example, a point in time when one end of the connector member contacts at least a portion of the sensor unit may be the start point of use 410 . For example, when 80 Units or more of drugs are injected from the drug injection device to the patient, the drug injection device may be switched from the inactive mode to the active mode.
컨트롤러는 약물 주입 장치와 데이터를 송수신하며 약물 주입 장치를 제어할 수 있다.The controller transmits and receives data to and from the drug injection device and may control the drug injection device.
컨트롤러는, 약물 주입 장치의 사용 가능 기간 및 사용자 설정 시간에 기초하여, 사용 개시 시점(410)으로부터 소정의 기간이 지난 제1 시점(420)에 약물 주입 장치의 사용 기간 만료가 임박하였다는 만료 임박 알림을 제공할 수 있다. 예를 들어, 제1 시점(420)은 만료 알림을 제공하는 시점의 1시간 전부터 24시간 전까지 중 임의의 시점으로 설정될 수 있다.Based on the usable period of the drug injection device and the user set time, the controller determines that the expiration of the use period of the drug injection device is imminent at the first time point 420 after a predetermined period has passed from the start time point 410 of use. Notifications can be provided. For example, the first time point 420 may be set to any time from 1 hour to 24 hours before the time when the expiration notification is provided.
또한, 컨트롤러는 사용 개시 시점(410)으로부터 사용 가능 기간이 지난 제2 시점(430)에 약물 주입 장치의 사용 기간이 만료되었다는 만료 알림을 제공할 수 있다.Also, the controller may provide an expiration notification indicating that the use period of the drug injection device has expired at a second time point 430 after the usable period has passed from the use start time 410 .
일 실시예에서, 약물 주입 장치의 사용 가능 기간은, 약물 주입 장치로부터 사용자에게 약물이 주입되는 동안, 사용자 인체에 삽입된 상태로 유지되는 대상체의 소재 및 상기 소재에 코팅되는 물질(예를 들어, 멤브레인 등) 중 적어도 어느 하나에 기초하여 결정될 수 있다. 다른 실시예에서, 약물 주입 장치의 사용 가능 기간은, 약물 주입 장치로부터 사용자에게 약물이 주입되는 동안, 사용자 인체에 삽입된 상태로 유지되는 대상체의 구조에 기초하여 결정될 수 있다. 즉, 약물 주입 장치의 사용 가능 기간은 대상체가 얼마나 오랜 기간 이상 없이 사용자 인체에 삽입된 상태로 유지될 수 있는지에 따라 결정될 수 있다.In one embodiment, the usable period of the drug injection device is, while the drug is injected from the drug injection device to the user, the material of the object that is kept inserted into the user's body and the material coated on the material (eg, membrane, etc.) may be determined based on at least one of. In another embodiment, the usable period of the drug injection device may be determined based on the structure of the object maintained in a state of being inserted into the user's body while the drug is injected from the drug injection device to the user. That is, the usable period of the drug injection device may be determined according to how long the object can be maintained while being inserted into the user's body.
도 3을 참조하여 설명하면, 저장부(201)에 약물이 저장된 후, 약물 주입 장치(1)는 사용자에게 부착된다. 사용자는 약물 주입 장치(1)를 사용자에게 부착하고, 니들 조립체(100)를 회전시켜, 니들(N) 및 캐뉼러를 피부에 삽입한다. 니들(N)은 캐뉼러와 함께 피부에 삽입되며, 캐뉼러가 피부에 삽입되는 것을 유도할 수 있다.Referring to FIG. 3 , after the drug is stored in the storage unit 201 , the drug injection device 1 is attached to the user. The user attaches the drug injection device 1 to the user, rotates the needle assembly 100, and inserts the needle N and the cannula into the skin. The needle N is inserted into the skin together with the cannula, and may induce the cannula to be inserted into the skin.
이후에 니들(N)은 피부에서 인출되되, 캐뉼러와 연결된 상태를 유지한다. 사용자가 니들 조립체(100)를 더 회전하면, 니들(N)은 캐뉼러가 피부에 삽입된 상태에서 상부로 이동한다. 캐뉼러 및 니들(N)은 적어도 일부가 연결되고, 약액이 이동하는 경로를 형성 및 유지한다. Afterwards, the needle (N) is withdrawn from the skin, maintaining a state connected to the cannula. When the user further rotates the needle assembly 100, the needle N moves upward while the cannula is inserted into the skin. At least a part of the cannula and the needle (N) is connected, and forms and maintains a path through which the drug solution moves.
즉, 저장부(201)로부터 사용자에게 약물이 주입되는 동안 캐뉼러는 사용자 인체에 삽입된 상태로 유지되고, 저장부(201)에 저장된 약물은 캐뉼러를 통해 사용자에게 주입될 수 있다.That is, while the drug is injected from the storage unit 201 to the user, the cannula is maintained in a state inserted into the user's body, and the drug stored in the storage unit 201 may be injected to the user through the cannula.
이처럼 사용자에게 약물이 주입되는 동안 캐뉼러가 사용자 인체에 삽입된 상태로 유지되는 경우, 약물 주입 장치의 사용 가능 기간은 캐뉼러의 소재에 기초하여 결정될 수 있다. 캐뉼러의 소재에 따라 캐뉼러가 인체에 삽입된 상태로 유지될 때 안전성이 보장되는 기간은 달라질 수 있으므로, 캐뉼러의 소재에 따라 약물 주입 장치의 사용 가능 기간은 다르게 설정될 수 있다.As such, when the cannula remains inserted into the user's body while the drug is injected to the user, the usable period of the drug injection device may be determined based on the material of the cannula. Depending on the material of the cannula, the period for which safety is ensured when the cannula is maintained in a state of being inserted into the human body may vary.
예를 들어, 캐뉼러의 소재는 테프론(Teflon)을 포함할 수 있고, 이 경우 약물 주입 장치의 사용 가능 기간은 3.5일로 설정될 수 있다. 사용 개시 시점(410)으로부터 사용 가능 기간에 해당하는 3.5일(84시간)이 지난 제2 시점(430)에, 컨트롤러는 약물 주입 장치의 사용 기간이 만료되었다는 만료 알림을 제공할 수 있다. 한편, 캐뉼러의 소재로 테프론 뿐만 아니라 다른 물질이 더 포함되거나, 테프론이 아닌 다른 물질이 포함되는 경우, 사용 가능 기간은 다르게 설정될 수 있다.For example, the material of the cannula may include Teflon, and in this case, the usable period of the drug injection device may be set to 3.5 days. At a second time point 430 after 3.5 days (84 hours), which corresponds to the usable period from the start time 410 of use, the controller may provide an expiration notification indicating that the use period of the drug injection device has expired. On the other hand, when other materials as well as Teflon are included as the material of the cannula, or when a material other than Teflon is included, the usable period may be set differently.
사용자는 약물 주입 장치의 사용 가능 기간이 도과하기 전의 임의의 시간을 설정함으로써, 만료 임박 알림을 제공받을 수 있다. 예를 들어, 약물 주입 장치의 사용 가능 기간은 3.5일(84시간)로 설정되고, 사용자 설정 시간이 1시간인 경우, 사용 개시 시점(410)으로부터 83시간(84시간-1시간)이 지난 제1 시점(420)에 컨트롤러는 약물 주입 장치의 사용 기간 만료가 임박하였다는 만료 임박 알림을 제공할 수 있다.The user may be provided with an imminent expiration notification by setting an arbitrary time before the usable period of the drug injection device has elapsed. For example, if the usable period of the drug injection device is set to 3.5 days (84 hours), and the user set time is 1 hour, 83 hours (84 hours - 1 hour) have elapsed from the start time 410 of use. At one time point 420 , the controller may provide an imminent expiration notification indicating that the expiration date of the use period of the drug injection device is imminent.
한편, 이상에서는 사용자 인체에 캐뉼러가 삽입된 채로 유지되는 것을 전제로, 약물 주입 장치의 사용 가능 기간이 캐뉼러의 소재에 기초하여 결정되는 것으로 기재하였으나, 인체에 니들(N)이 삽입된 채로 유지되는 경우 약물 주입 장치의 사용 가능 기간은 니들(N)의 소재에 기초하여 결정될 수 있다. Meanwhile, in the above description, on the premise that the cannula remains inserted into the user's body, the usable period of the drug injection device has been described as being determined based on the material of the cannula, but with the needle (N) inserted into the body If maintained, the usable period of the drug injection device may be determined based on the material of the needle (N).
다른 실시예에서, 약물 주입 장치의 사용 가능 기간은, 저장부 용량 및 하루 평균 투여량에 기초하여 결정될 수 있다.In another embodiment, the usable period of the drug injection device may be determined based on the storage capacity and the average daily dose.
저장부 용량과 하루 평균 투여량은 unit 단위로 표기될 수 있다. unit 단위는 저장부에 저장된 약물이 구동부 펌프에 의해 인체로 주입될 때의 최소 단위를 의미할 수 있다.The storage capacity and the average daily dose may be expressed in units of units. The unit unit may mean a minimum unit when the drug stored in the storage unit is injected into the human body by the driving unit pump.
하루 평균 투여량은 환자 개인별 하루 평균 투여량이 아닌 복수의 환자들의 투여량 통계에 의해 산출되는 하루 평균 투여량일 수 있다. 하루 평균 투여량은 몇 형 당뇨를 앓는 환자의 투여량 통계에 의해 산출되었는지에 따라 달라질 수 있다. 예를 들어, 1형 당뇨를 앓는 환자의 하루 평균 투여량보다 2형 당뇨를 앓는 환자의 하루 평균 투여량이 더 많게 설정될 수 있다.The average daily dose may be an average daily dose calculated by the dose statistics of a plurality of patients, rather than the average daily dose for each individual patient. The average daily dose may vary depending on the number of type diabetes patients calculated by the dose statistics. For example, the average daily dose of patients with type 2 diabetes may be set to be higher than the average daily dose of patients with type 1 diabetes.
또한, 하루 평균 투여량은 약물 주입 장치에 저장된 약물의 농도에 따라 달라질 수 있다. 예를 들어, 1ml에 100Unit 들어있는 약물이 환자에게 투여되는 경우와, 1ml에 200Unit 또는 500Unit 들어있는 약물이 환자에게 투여되는 경우, 하루 평균 투여량은 다르게 설정될 수 있다.In addition, the average daily dose may vary depending on the concentration of the drug stored in the drug injection device. For example, when a drug containing 100Unit in 1ml is administered to a patient, and when a drug containing 200Unit or 500Unit in 1ml is administered to a patient, the average daily dose may be set differently.
저장부 용량이 200 unit이고, 하루 평균 투여량이 60 unit인 경우, 약물 주입 장치의 사용 가능 기간은 3.5일(200unit/60unit=3.5)로 설정될 수 있다. 이 경우, 사용 개시 시점(410)으로부터 사용 가능 기간에 해당하는 3.5일이 지난 제2 시점(430)에, 컨트롤러는 약물 주입 장치의 사용 기간이 만료되었다는 만료 알림을 제공할 수 있다.When the storage capacity is 200 units and the average daily dose is 60 units, the usable period of the drug injection device may be set to 3.5 days (200unit/60unit=3.5). In this case, at the second time point 430 after 3.5 days corresponding to the usable period from the start time 410 of use, the controller may provide an expiration notification indicating that the use period of the drug injection device has expired.
또한, 사용자는 약물 주입 장치의 사용 가능 기간에 도달하기 전의 임의의 시간을 설정함으로써, 사용 가능 기간 도달 전에 만료 임박 알림을 제공받을 수 있다. 예를 들어, 약물 주입 장치의 사용 가능 기간은 3.5일(84시간)로 설정되고, 사용자 설정 시간이 1시간인 경우, 사용 개시 시점(410)으로부터 83시간(84시간-1시간)이 지난 제1 시점(420)에 컨트롤러는 약물 주입 장치의 사용 기간 만료가 임박하였다는 만료 임박 알림을 제공할 수 있다.In addition, by setting an arbitrary time before the usable period of the drug injection device is reached, the user may be provided with an imminent expiration notification before the usable period is reached. For example, if the usable period of the drug injection device is set to 3.5 days (84 hours), and the user set time is 1 hour, 83 hours (84 hours - 1 hour) have elapsed from the start time 410 of use. At one time point 420 , the controller may provide an imminent expiration notification indicating that the expiration date of the use period of the drug injection device is imminent.
한편, 저장부 용량과 하루 평균 투여량이 달라지는 경우, 약물 주입 장치의 사용 가능 기간은 달라질 수 있다.On the other hand, when the storage capacity and the average daily dose are different, the usable period of the drug injection device may vary.
또 다른 실시예에서, 약물 주입 장치의 사용 가능 기간은, 약물 주입 장치로부터 사용자에게 약물이 주입되는 동안 사용자 인체에 삽입된 상태로 유지되는 대상체의 소재, 상기 소재에 코팅되는 물질 및 상기 대상체의 구조 중 적어도 하나, 저장부 용량 및 하루 평균 투여량에 기초하여 결정될 수 있다.In another embodiment, the usable period of the drug injection device is the material of the object that remains inserted into the user's body while the drug is injected from the drug injection device to the user, the material coated on the material, and the structure of the object It may be determined based on at least one of, the storage capacity and the average daily dose.
구체적으로, 컨트롤러는, 캐뉼러가 인체에 삽입된 상태로 유지될 때 안전성이 보장되는 제1 기간과, 저장부 용량 및 하루 평균 투여량에 기초하여 산출된 제2 기간을 비교하여 약물 주입 장치의 사용 가능 기간을 결정할 수 있다.Specifically, the controller compares the first period in which safety is ensured when the cannula is maintained in a state inserted into the human body and the second period calculated based on the storage capacity and the average daily dose of the drug injection device. You can decide how long you can use it.
예를 들어, 캐뉼러가 인체에 삽입된 상태로 유지될 때 안전성이 보장되는 제1 기간이 4일이고, 저장부 용량 및 하루 평균 투여량에 기초하여 산출된 제2 기간이 3일인 경우, 제2 시점(430)은 제1 기간(4일)과 제2 기간(3일) 중 더 짧은 기간인 3일로 설정될 수 있다.For example, if the first period for which safety is ensured when the cannula is kept inserted into the human body is 4 days, and the second period calculated based on the storage capacity and the average daily dose is 3 days, the second period The second time point 430 may be set to 3 days, which is the shorter period of the first period (4 days) and the second period (3 days).
또는, 캐뉼러가 인체에 삽입된 상태로 유지될 때 안전성이 보장되는 제1 기간이 3.5일이고, 저장부 용량 및 하루 평균 투여량에 기초하여 산출된 제2 기간이 4일인 경우, 제2 시점(430)은 제1 기간(3.5일)과 제2 기간(4일) 중 더 짧은 기간인 3.5일로 설정될 수 있다.Alternatively, when the first period for which safety is ensured when the cannula is maintained in the human body is 3.5 days, and the second period calculated based on the storage capacity and the average daily dose is 4 days, the second time point 430 may be set to 3.5 days, which is a shorter period of the first period (3.5 days) and the second period (4 days).
한편, 사용자 인체에 삽입된 상태로 유지되는 대상체의 소재가 변경된다거나, 저장부 용량이 변경된다거나, 하루 평균 투여량이 변경될 경우, 컨트롤러는 변경 사항을 고려하여 약물 주입 장치의 사용 가능 기간을 업데이트할 수 있다.On the other hand, if the material of the object kept inserted into the user's body is changed, the storage capacity is changed, or the average daily dose is changed, the controller adjusts the usable period of the drug injection device in consideration of the change. can be updated.
컨트롤러는 약물 주입 장치를 통해 만료 임박 알림 및 만료 알림을 제공할 수 있다. 또는, 컨트롤러는 직접 만료 임박 알림 및 만료 알림을 제공할 수 있다. 또는, 컨트롤러는 사용자 단말로 데이터를 전송하고, 사용자 단말에서 만료 임박 알림 및 만료 알림을 제공할 수 있다.The controller may provide an imminent expiration notification and an expiration notification via the drug infusion device. Alternatively, the controller may directly provide an imminent expiration notification and an expiration notification. Alternatively, the controller may transmit data to the user terminal and provide an imminent expiration notification and an expiration notification from the user terminal.
도 5는 일 실시예에 따른 약물 주입 장치의 사용 기간에 따른 알림을 제공하는 예시를 설명하기 위한 도면이다.5 is a view for explaining an example of providing a notification according to the period of use of the drug injection device according to an embodiment.
도 5를 참조하면, 도 4와 비교하여, 약물 주입 장치의 사용 기간 만료가 임박하였다는 만료 임박 알림을 제공하는 제1 시점(520)과, 약물 주입 장치의 사용 기간이 만료되었다는 만료 알림을 제공하는 제2 시점(530) 외에, 제3 시점(550) 및 제4 시점(540)이 더 추가된 타임라인이 도시된다.Referring to FIG. 5 , as compared with FIG. 4 , a first time point 520 for providing an imminent expiration notification indicating that the expiration date of the drug injection device is imminent, and an expiration notification indicating that the usage period of the drug injection device has expired In addition to the second viewpoint 530 , a timeline to which a third viewpoint 550 and a fourth viewpoint 540 are further added is shown.
약물 주입 장치는 사용 가능 기간 외에 서비스 기간을 더 포함할 수 있다. 약물 주입 장치는 사용 가능 기간 및 서비스 기간 동안 활성 모드에서 동작할 수 있다. 즉, 약물 주입 장치는 사용 가능 기간이 도과하더라도 서비스 기간 동안이 도과하지 않았다면 정상적으로 동작할 수 있다. The drug injection device may further include a service period in addition to the usable period. The drug infusion device may operate in an active mode during the usable period and the service period. That is, even if the usable period has elapsed, the drug injection device may operate normally if the service period does not elapse.
사용 가능 기간은 매뉴얼 들을 통해 사용자에게 알려진 기간인 반면, 서비스 기간은 사용자에게 알려지지 않은 기간일 수 있다. 약물 주입 장치는 서비스 기간에도 활성 모드에서 정상적으로 동작하여 사용자에게 약물을 주입함으로써, 사용 가능 기간이 만료되더라도 일정 기간 동안 사용자는 약물 주입 장치로부터 약물을 주입 받을 수 있다.The usable period may be a period known to the user through the manuals, whereas the service period may be a period unknown to the user. The drug injection device operates normally in the active mode even during the service period and injects the drug to the user, so that the user can receive the drug from the drug injection device for a certain period even when the usable period expires.
컨트롤러는, 약물 주입 장치의 사용 가능 기간, 서비스 기간 및 사용자 설정 시간에 기초하여, 사용 개시 시점(510)으로부터 소정의 기간이 지난 제4 시점(540)에 약물 주입 장치의 폐기가 임박하였다는 폐기 임박 알림을 제공할 수 있다. 제4 시점(540)은 사용 개시 시점(510)으로부터 사용 가능 기간 및 서비스 기간이 도과하기 전의 시점이다.The controller, based on the usable period of the drug injection device, the service period, and the user set time, discards that the drug injection device is about to be discarded at a fourth time point 540 after a predetermined period has passed from the use start time 510 . An imminent notification can be provided. The fourth time point 540 is a time point before the usable period and the service period elapse from the use start time 510 .
또한, 컨트롤러는 사용 개시 시점(510)으로부터 사용 가능 기간 및 서비스 기간이 지난 제3 시점(550)에 약물 주입 장치가 폐기되어야 한다는 폐기 알림을 제공할 수 있다. 예를 들어, 제3 시점(550)은 제2 시점(540) 이후 12시간이 경과된 시간일 수 있다.In addition, the controller may provide a discard notification indicating that the drug injection device should be discarded at a third time point 550 after the usable period and service period from the start of use 510 . For example, the third time point 550 may be a time when 12 hours have passed since the second time point 540 .
일 실시예에서, 약물 주입 장치의 사용 가능 기간 및 서비스 기간은, 약물 주입 장치로부터 사용자에게 약물이 주입되는 동안, 사용자 인체에 삽입된 상태로 유지되는 대상체의 소재, 상기 소재에 코팅되는 물질 및 상기 대상체의 구조 중 적어도 하나에 기초하여 결정될 수 있다.In one embodiment, the usable period and service period of the drug injection device are, while the drug is injected from the drug injection device to the user, the material of the object that remains inserted into the user's body, the material coated on the material, and the It may be determined based on at least one of the structures of the object.
사용자에게 약물이 주입되는 동안 캐뉼러가 사용자 인체에 삽입된 상태로 유지되는 경우, 약물 주입 장치의 사용 가능 기간 및 서비스 기간은 캐뉼러의 소재에 기초하여 결정될 수 있다. 캐뉼러의 소재에 따라 캐뉼러가 인체에 삽입된 상태로 유지될 때 안전성이 보장되는 기간은 달라질 수 있으므로, 캐뉼러의 소재에 따라 약물 주입 장치의 사용 가능 기간 및 서비스 기간은 다르게 설정될 수 있다.When the cannula remains inserted into the user's body while the drug is being injected into the user, the usable period and service period of the drug injection device may be determined based on the material of the cannula. Depending on the material of the cannula, the period for which safety is guaranteed when the cannula is maintained in the human body may vary, so the usable period and service period of the drug injection device may be set differently depending on the material of the cannula .
예를 들어, 캐뉼러의 소재는 테프론(Teflon)을 포함할 수 있고, 이 경우 약물 주입 장치의 사용 가능 기간 및 서비스 기간은 4일로 설정될 수 있다. 사용 개시 시점(510)으로부터 사용 가능 기간 및 서비스 기간에 해당하는 4일(96시간)이 지난 제3 시점(550)에, 컨트롤러는 약물 주입 장치가 폐기되어야 한다는 폐기 알림을 제공할 수 있다. 한편, 캐뉼러의 소재로 테프론 뿐만 아니라 다른 물질이 더 포함된다거나, 테프론이 아닌 다른 물질이 포함되는 경우, 사용 가능 기간은 다르게 설정될 수 있다.For example, the material of the cannula may include Teflon, and in this case, the usable period and service period of the drug injection device may be set to 4 days. At a third time point 550 after 4 days (96 hours), which corresponds to the usable period and the service period, from the starting point of use 510, the controller may provide a discard notification indicating that the drug injection device should be discarded. On the other hand, when other materials as well as Teflon are included as the material of the cannula, or when a material other than Teflon is included, the usable period may be set differently.
사용자는 약물 주입 장치의 사용 가능 기간 도과 후 서비스 기간 도과 전의 임의의 시간을 설정함으로써, 폐기 임박 알림을 제공받을 수 있다. 예를 들어, 약물 주입 장치의 사용 가능 기간 및 서비스 기간은 4일(96시간)로 설정되고, 사용자 설정 시간이 1시간인 경우, 사용 개시 시점(510)으로부터 95시간(96시간-1시간)이 지난 제4 시점(540)에 컨트롤러는 약물 주입 장치의 폐기가 임박하였다는 기간 만료가 임박하였다는 폐기 임박 알림을 제공할 수 있다.The user may be provided with an imminent disposal notification by setting an arbitrary time before the expiration of the service period after the expiration of the usable period of the drug injection device. For example, the usable period and service period of the drug injection device are set to 4 days (96 hours), and when the user set time is 1 hour, 95 hours (96 hours - 1 hour) from the start of use 510 At this last fourth time point 540 , the controller may provide an imminent disposal notification indicating that the expiry of the period indicating that the drug injection device is imminent is imminent.
다른 실시예에서, 약물 주입 장치의 사용 가능 기간 및 서비스 기간은, 저장부 용량 및 하루 평균 투여량에 기초하여 결정될 수 있다.In another embodiment, the usable period and service period of the drug injection device may be determined based on the storage capacity and the average daily dose.
저장부 용량이 240 unit이고, 하루 평균 투여량이 60 unit인 경우, 약물 주입 장치의 사용 가능 기간은 4일(240unit/60unit=4)로 설정될 수 있다. 이 경우, 사용 개시 시점(510)으로부터 사용 가능 기간 및 서비스 기간에 해당하는 4일이 지난 제3 시점(550)에, 컨트롤러는 약물 주입 장치가 폐기되어야 한다는 폐기 알림을 제공할 수 있다.When the storage capacity is 240 units, and the average daily dose is 60 units, the usable period of the drug injection device may be set to 4 days (240unit/60unit=4). In this case, at a third time point 550 that has passed 4 days corresponding to the usable period and service period from the use start time 510 , the controller may provide a discard notification indicating that the drug injection device should be discarded.
또한, 사용자는 약물 주입 장치의 사용 가능 기간 도과 후 서비스 기간 도과 전의 임의의 시간을 설정함으로써, 폐기 임박 알림을 제공받을 수 있다. 예를 들어, 약물 주입 장치의 사용 가능 기간 및 서비스 기간은 4일(96시간)로 설정되고, 사용자 설정 시간이 1시간인 경우, 사용 개시 시점(510)으로부터 96시간(96시간-1시간)이 지난 제4 시점(540)에 컨트롤러는 약물 주입 장치의 폐기가 임박하였다는 폐기 임박 알림을 제공할 수 있다.In addition, the user may be provided with an imminent disposal notification by setting an arbitrary time before the expiration of the service period after the expiration of the usable period of the drug injection device. For example, the usable period and service period of the drug injection device are set to 4 days (96 hours), and when the user set time is 1 hour, 96 hours (96 hours - 1 hour) from the start time of use 510 At this last fourth time point 540 , the controller may provide an imminent disposal notification indicating that the disposal of the drug injection device is imminent.
또 다른 실시예에서, 약물 주입 장치의 사용 가능 기간 및 서비스 기간은, 약물 주입 장치로부터 사용자에게 약물이 주입되는 동안 사용자 인체에 삽입된 상태로 유지되는 대상체의 소재, 상기 소재에 코팅되는 물질 및 상기 대상체의 구조 중 적어도 하나, 저장부 용량 및 하루 평균 투여량에 기초하여 결정될 수 있다.In another embodiment, the usable period and service period of the drug injection device include the material of the object that remains inserted into the user's body while the drug is injected from the drug injection device to the user, the material coated on the material, and the It may be determined based on at least one of the subject's structures, the storage capacity, and the average daily dose.
구체적으로 컨트롤러는, 캐뉼러가 인체에 삽입된 상태로 유지될 때 안전성이 보장되는 제1 기간과, 저장부 용량 및 하루 평균 투여량에 기초하여 산출된 제2 기간을 비교하여 약물 주입 장치의 사용 가능 기간 및 서비스 기간을 결정할 수 있다.Specifically, the controller compares the first period in which safety is ensured when the cannula is kept inserted into the human body and the second period calculated based on the storage capacity and the average daily dose to use the drug injection device. It is possible to determine the available period and service period.
예를 들어, 캐뉼러가 인체에 삽입된 상태로 유지될 때 안전성이 보장되는 제1 기간이 4일이고, 저장부 용량 및 하루 평균 투여량에 기초하여 산출된 제2 기간이 3일인 경우, 제3 시점(550)은 제1 기간(4일)과 제2 기간(3일) 중 더 짧은 기간인 3일로 설정될 수 있다.For example, if the first period for which safety is ensured when the cannula is kept inserted into the human body is 4 days, and the second period calculated based on the storage capacity and the average daily dose is 3 days, the second period The three time points 550 may be set to 3 days, which is the shorter period of the first period (4 days) and the second period (3 days).
또는, 캐뉼러가 인체에 삽입된 상태로 유지될 때 안전성이 보장되는 제1 기간이 3.5일이고, 저장부 용량 및 하루 평균 투여량에 기초하여 산출된 제2 기간이 4일인 경우, 제3 시점(550)은 제1 기간(3.5일)과 제2 기간(4일) 중 더 짧은 기간인 3.5일로 설정될 수 있다.Alternatively, when the first period for which safety is ensured when the cannula is maintained in the human body is 3.5 days, and the second period calculated based on the storage capacity and the average daily dose is 4 days, the third time point 550 may be set to 3.5 days, which is a shorter period of the first period (3.5 days) and the second period (4 days).
한편, 약물 주입 장치의 사용 기간 만료가 임박하였다는 제1 시점(520)과, 약물 주입 장치의 사용이 만료되었다는 만료 알림을 제공하는 제2 시점(530)은 임의로 설정될 수 있다. 예를 들어, 제3 시점(550)이 사용 개시 시점(510)으로부터 4일(96시간)이 지난 후로 설정된 경우, 제2 시점(530)은 사용 개시 시점(510)으로부터 3.5일(84시간)이 지난 후로 설정되고, 제1 시점(520)은 사용 개시 시점(510)으로부터 83시간이 지난 후로 설정될 수 있다.Meanwhile, a first time point 520 indicating that the use period of the drug injection device is about to expire and a second time point 530 for providing an expiration notification indicating that the use of the drug injection device has expired may be arbitrarily set. For example, if the third time point 550 is set to 4 days (96 hours) after the use start time 510 has elapsed, the second time point 530 is 3.5 days (84 hours) from the use start time 510 . is set after the lapse of , and the first time point 520 may be set after 83 hours have elapsed from the use start time point 510 .
다른 실시예에서, 약물 주입 장치의 사용 가능 기간은 저장부 용량 및 하루 평균 투여량에 기초하여 결정되고, 약물 주입 장치의 사용 가능 기간과 서비스 기간을 더한 총 기간은, 약물 주입 장치로부터 사용자에게 약물이 주입되는 동안 사용자 인체에 삽입된 상태로 유지되는 대상체의 소재, 상기 소재에 코팅되는 물질 및 상기 대상체의 구조 중 적어도 하나에 기초하여 결정될 수 있다.In another embodiment, the usable period of the drug infusion device is determined based on the storage capacity and the average daily dose, and the total period of the drug infusion device plus the service period is the drug from the drug infusion device to the user. This may be determined based on at least one of a material of the object maintained in a state inserted into the user's body during the injection, a material coated on the material, and a structure of the object.
구체적으로 컨트롤러는, 캐뉼러가 인체에 삽입된 상태로 유지될 때 안전성이 보장되는 제1 기간을 총 기간으로 결정하고, 저장부 용량 및 하루 평균 투여량에 기초하여 산출된 제2 기간을 사용 가능 기간으로 결정할 수 있다.Specifically, the controller may determine a first period for which safety is ensured when the cannula is maintained in the human body as the total period, and use the second period calculated based on the storage capacity and the average daily dose period can be determined.
예를 들어, 캐뉼러가 인체에 삽입된 상태로 유지될 때 안전성이 보장되는 제1 기간이 4일이고, 저장부 용량 및 하루 평균 투여량에 기초하여 산출된 제2 기간이 3일인 경우, 제3 시점(550)은 제1 기간인 4일로 설정되고, 제2 시점(530)은 제2 기간은 3일로 설정될 수 있다.For example, if the first period for which safety is ensured when the cannula is kept inserted into the human body is 4 days, and the second period calculated based on the storage capacity and the average daily dose is 3 days, the second period The third time point 550 may be set as a first period of 4 days, and the second time point 530 may be set as a second period of 3 days.
즉, 본 발명에서는 저장부 내 약물이 고갈된 때 사용자에게 만료 알림을 제공하고, 인체에 삽입된 대상체의 안전성 보장 기간에 기초하여 폐기 알림을 제공함으로써, 다양한 종류의 알림을 통해 사용자에게 편의성을 제공할 수 있다.That is, in the present invention, when the drug in the storage unit is exhausted, an expiration notification is provided to the user, and a disposal notification is provided based on the safety guarantee period of the object inserted into the human body, thereby providing convenience to the user through various types of notifications. can do.
만료 임박 알림, 만료 알림, 폐기 임박 알림 및 폐기 알림을 제공하는 방식은 서로 상이할 수 있다. 각 알림의 진동 주기, 진동 세기, LED 색상 표시, LED 점멸 주기 및 알림 반복 주기 등은 서로 상이할 수 있다. 사용자는 알림이 제공되는 방식만으로도 해당 알림이 만료 임박 알림, 만료 알림, 폐기 임박 알림 및 폐기 알림 중 어느 알림에 해당하는지 용이하게 파악할 수 있다.Methods of providing an imminent expiration notification, an expiration notification, an imminent retirement notification, and a retirement notification may be different from each other. The vibration cycle, vibration intensity, LED color display, LED blinking cycle, and notification repeat cycle of each notification may be different from each other. The user can easily determine whether the notification corresponds to an imminent expiration notification, an expiration notification, an imminent retirement notification, or a retirement notification only by the manner in which the notification is provided.
도 6은 일 실시예에 따른 약물 주입 장치의 사용 기간에 따른 알림을 제공하는 방법의 흐름도이다.6 is a flowchart of a method of providing a notification according to the period of use of the drug injection device according to an embodiment.
컨트롤러는 약물 주입 장치와 통신을 수행할 수 있다. 컨트롤러는 스마트폰, PC 등과 같은 사용자 단말에 포함된 구성이거나, 사용자 단말과는 독립된 구성일 수 있다. 또는, 컨트롤러는 약물 주입 장치에 포함된 구성일 수도 있다. 이하에서는, 약물 주입 장치와 컨트롤러가 네트워크를 이용하여 통신을 수행하는 것을 전제로 한다.The controller may communicate with the drug injection device. The controller may be a component included in a user terminal such as a smart phone or a PC, or may be a component independent of the user terminal. Alternatively, the controller may be a component included in the drug injection device. Hereinafter, it is assumed that the drug injection device and the controller perform communication using a network.
단계 610에서, 컨트롤러는 약물 주입 장치가 비활성 모드에서 활성 모드로 전환되는 시점을 사용 개시 시점으로 결정할 수 있다.In operation 610, the controller may determine a time when the drug injection device is switched from the inactive mode to the active mode as the start time of use.
약물 주입 장치는 소정의 동작에 의해 비활성 모드에서 활성 모드로 전환될 수 있다. 예를 들어, 소정의 동작은 약물 보충 동작일 수 있다. 구체적으로, 저장부에 약물이 보충됨에 따라 저장부의 커버와 연결된 플런저가 선형 이동하면서 플런저와 연결된 커넥터 부재의 일단부가 센서 유닛의 적어도 일부에 접촉할 수 있다. 커넥터 부재의 일단부가 센서 유닛의 적어도 일부에 접촉한 경우, 약물 주입 장치는 비활성 모드에서 활성 모드로 전환될 수 있다.The drug injection device may be switched from an inactive mode to an active mode by a predetermined operation. For example, the predetermined operation may be a drug replenishment operation. Specifically, as the drug is replenished in the reservoir, one end of the connector member connected to the plunger may be in contact with at least a portion of the sensor unit while the plunger connected to the cover of the reservoir moves linearly. When one end of the connector member contacts at least a part of the sensor unit, the drug injection device may be switched from the inactive mode to the active mode.
약물 주입 장치는 활성 모드 전환 신호를 컨트롤러로 전송할 수 있다. 컨트롤러는 약물 주입 장치로부터 활성 모드 전환 신호를 수신한 시점을 사용 개시 시점으로 결정할 수 있다.The drug injection device may transmit an active mode switching signal to the controller. The controller may determine the time when the active mode switching signal is received from the drug injection device as the start time of use.
한편, 컨트롤러가 약물 주입 장치로부터 활성 모드 전환 신호를 수신하기 위해서는, 컨트롤러와 약물 주입 장치 간의 통신 네트워크가 형성되어야 한다. On the other hand, in order for the controller to receive the active mode switching signal from the drug injection device, a communication network between the controller and the drug injection device must be formed.
약물 주입 장치가 비활성 모드에서 활성 모드로 전환된 시점에 컨트롤러와 약물 주입 장치 간의 통신 네트워크가 형성되어 있지 않을 수 있다. 이 경우, 약물 주입 장치와 컨트롤러 간 통신 네트워크가 형성된 시점에, 약물 주입 장치는 컨트롤러로 활성 모드로 전환되어 경과된 시간 정보를 전송할 수 있다.When the drug injection device is switched from the inactive mode to the active mode, a communication network between the controller and the drug injection device may not be formed. In this case, when the communication network between the drug injection device and the controller is formed, the drug injection device may be switched to the active mode with the controller to transmit elapsed time information.
단계 620에서, 컨트롤러는 약물 주입 장치의 사용 가능 기간 및 사용자 설정 시간에 기초하여, 사용 개시 시점으로부터 소정의 기간이 지난 제1 시점에 약물 주입 장치의 사용 기간 만료가 임박하였다는 만료 임박 알림을 제공할 수 있다.In step 620, the controller provides an expiration imminent notification indicating that the expiration date of the drug injection device is imminent at a first time point when a predetermined period has passed from the start of use, based on the usable period of the drug injection device and the user set time can do.
단계 630에서, 컨트롤러는 사용 개시 시점으로부터 사용 가능 기간이 지난 제2 시점에 약물 주입 장치의 사용 기간이 만료되었다는 만료 알림을 제공할 수 있다.In operation 630 , the controller may provide an expiration notification indicating that the use period of the drug injection device has expired at a second time point when the usable period has passed from the start of use.
일 실시예에서, 약물 주입 장치의 사용 가능 기간은, 약물 주입 장치로부터 사용자에게 약물이 주입되는 동안, 사용자 인체에 삽입된 상태로 유지되는 대상체의 소재에 기초하여 결정될 수 있다. 다른 실시예에서, 약물 주입 장치의 사용 가능 기간은, 저장부 용량 및 하루 평균 투여량에 기초하여 결정될 수 있다. 또 다른 실시예에서, 약물 주입 장치의 사용 가능 기간은, 약물 주입 장치로부터 사용자에게 약물이 주입되는 동안 사용자 인체에 삽입된 상태로 유지되는 대상체의 소재, 저장부 용량 및 하루 평균 투여량에 기초하여 결정될 수 있다.In an embodiment, the usable period of the drug injection device may be determined based on the material of the object maintained in the user's body while the drug is injected from the drug injection device to the user. In another embodiment, the usable period of the drug injection device may be determined based on the storage capacity and the average daily dose. In another embodiment, the usable period of the drug injection device is based on the material of the subject, the storage capacity, and the average daily dose of the subject that remains inserted into the user's body while the drug is injected from the drug injection device to the user. can be decided.
한편, 약물 주입 장치는 사용 가능 기간 외에 서비스 기간을 더 포함할 수 있다. 약물 주입 장치는 사용 가능 기간 및 서비스 기간 동안 활성 모드에서 동작할 수 있다. 즉, 약물 주입 장치는 사용 가능 기간이 도과하더라도 서비스 기간 동안이 도과하지 않았다면 정상적으로 동작할 수 있다.Meanwhile, the drug injection device may further include a service period in addition to the usable period. The drug infusion device may operate in an active mode during the usable period and the service period. That is, even if the usable period has elapsed, the drug injection device may operate normally if the service period does not elapse.
약물 주입 장치는 사용 가능 기간 외에 서비스 기간을 더 포함하는 경우, 컨트롤러는 약물 주입 장치의 사용 가능 기간, 서비스 기간 및 사용자 설정 시간에 기초하여, 사용 개시 시점으로부터 소정의 기간이 지난 제4 시점에 약물 주입 장치의 폐기가 임박하였다는 폐기 임박 알림을 제공할 수 있다. 제4 시점은 사용 개시 시점(510)으로부터 사용 가능 기간 및 서비스 기간이 도과하기 전의 시점이다.When the drug injection device further includes a service period in addition to the usable period, the controller controls the drug at a fourth time point after a predetermined period from the start of use based on the usable period, service period, and user set time of the drug injection device. An imminent disposal notification may be provided that the disposition of the injection device is imminent. The fourth time point is a time point before the usable period and service period elapse from the use start time 510 .
또한, 컨트롤러는 사용 개시 시점으로부터 사용 가능 기간 및 서비스 기간이 지난 제3 시점에 약물 주입 장치가 폐기되어야 한다는 폐기 알림을 제공할 수 있다.In addition, the controller may provide a discard notification that the drug injection device should be discarded at a third time point after the usable period and the service period from the start of use.
일 실시예에서, 약물 주입 장치의 사용 가능 기간 및 서비스 기간은, 약물 주입 장치로부터 사용자에게 약물이 주입되는 동안, 사용자 인체에 삽입된 상태로 유지되는 대상체의 소재에 기초하여 결정될 수 있다. 다른 실시예에서, 약물 주입 장치의 사용 가능 기간 및 서비스 기간은, 저장부 용량 및 하루 평균 투여량에 기초하여 결정될 수 있다. 또 다른 실시예에서, 약물 주입 장치의 사용 가능 기간은, 약물 주입 장치로부터 사용자에게 약물이 주입되는 동안 사용자 인체에 삽입된 상태로 유지되는 대상체의 소재, 저장부 용량 및 하루 평균 투여량에 기초하여 결정될 수 있다.In an embodiment, the usable period and service period of the drug injection device may be determined based on the material of the object that is maintained in a state inserted into the user's body while the drug is injected from the drug injection device to the user. In another embodiment, the usable period and service period of the drug injection device may be determined based on the storage capacity and the average daily dose. In another embodiment, the usable period of the drug injection device is based on the material of the subject, the storage capacity, and the average daily dose of the subject that remains inserted into the user's body while the drug is injected from the drug injection device to the user. can be decided.
약물 주입 장치는 사용 가능 기간 외에 서비스 기간을 더 포함하는 경우, 약물 주입 장치의 사용 기간 만료가 임박하였다는 제1 시점과, 약물 주입 장치의 사용이 만료되었다는 만료 알림을 제공하는 제2 시점은 임의로 설정될 수 있다. When the drug injection device further includes a service period in addition to the usable period, the first time point indicating that the usage period of the drug injection device is imminent and the second time point for providing an expiration notification indicating that the use of the drug injection device has expired are arbitrarily can be set.
본 개시의 다양한 실시예들은 기기(machine) 의해 읽을 수 있는 저장 매체(storage medium)에 저장된 하나 이상의 명령어들을 포함하는 소프트웨어(예: 프로그램))로서 구현될 수 있다. 예를 들면, 기기의 프로세서는, 저장 매체로부터 저장된 하나 이상의 명령어들 중 적어도 하나의 명령을 호출하고, 그것을 실행할 수 있다. 이것은 기기가 상기 호출된 적어도 하나의 명령어에 따라 적어도 하나의 기능을 수행하도록 운영되는 것을 가능하게 한다. 상기 하나 이상의 명령어들은 컴파일러에 의해 생성된 코드 또는 인터프리터에 의해 실행될 수 있는 코드를 포함할 수 있다. 기기로 읽을 수 있는 저장매체는, 비일시적(non-transitory) 저장매체의 형태로 제공될 수 있다. 여기서, ‘비일시적’은 저장매체가 실재(tangible)하는 장치이고, 신호(signal)(예: 전자기파)를 포함하지 않는다는 것을 의미할 뿐이며, 이 용어는 데이터가 저장매체에 반영구적으로 저장되는 경우와 임시적으로 저장되는 경우를 구분하지 않는다.Various embodiments of the present disclosure may be implemented as software (eg, a program) including one or more instructions stored in a storage medium readable by a machine. For example, the processor of the device may call at least one of the one or more instructions stored from the storage medium and execute it. This makes it possible for the device to be operated to perform at least one function according to the called at least one command. The one or more instructions may include code generated by a compiler or code executable by an interpreter. The device-readable storage medium may be provided in the form of a non-transitory storage medium. Here, 'non-transitory' only means that the storage medium is a tangible device and does not contain a signal (eg, electromagnetic wave), and this term is used in cases where data is semi-permanently stored in the storage medium and It does not distinguish between temporary storage cases.
일 실시예에 따르면, 본 개시의 다양한 실시예들에 따른 방법은 컴퓨터 프로그램 제품(computer program product)에 포함되어 제공될 수 있다. 컴퓨터 프로그램 제품은 상품으로서 판매자 및 구매자 간에 거래될 수 있다. 컴퓨터 프로그램 제품은 기기로 읽을 수 있는 저장 매체(예: compact disc read only memory (CD-ROM))의 형태로 배포되거나, 또는 어플리케이션 스토어(예: 플레이 스토어TM)를 통해 또는 두 개의 사용자 장치들 간에 직접, 온라인으로 배포(예: 다운로드 또는 업로드)될 수 있다. 온라인 배포의 경우에, 컴퓨터 프로그램 제품의 적어도 일부는 제조사의 서버, 어플리케이션 스토어의 서버, 또는 중계 서버의 메모리와 같은 기기로 읽을 수 있는 저장 매체에 적어도 일시 저장되거나, 임시적으로 생성될 수 있다.According to an embodiment, the method according to various embodiments of the present disclosure may be provided by being included in a computer program product. Computer program products can be traded between sellers and buyers as commodities. Computer programs products are distributed in the form of a device-readable storage medium (eg compact disc read only memory (CD-ROM)), or through an application store (eg Play Store™) or between two user devices. It can be distributed directly or online (eg, downloaded or uploaded). In the case of online distribution, at least a part of a computer, a program, and a product may be temporarily stored or temporarily created in a machine-readable storage medium such as a server of a manufacturer, a server of an application store, or a memory of a relay server.
또한, 본 명세서에서, "부"는 프로세서 또는 회로와 같은 하드웨어 구성(hardware component), 및/또는 프로세서와 같은 하드웨어 구성에 의해 실행되는 소프트웨어 구성(software component)일 수 있다.Also, in this specification, "unit" may be a hardware component such as a processor or circuit, and/or a software component executed by a hardware component such as a processor.
본 실시예의 범위는 상기 상세한 설명보다는 후술하는 특허청구범위에 의하여 나타내어지며, 특허청구범위의 의미 및 범위 그리고 그 균등 개념으로부터 도출되는 모든 변경 또는 변형된 형태가 포함되는 것으로 해석되어야 한다.The scope of the present embodiment is indicated by the claims to be described later rather than the above detailed description, and it should be construed as including all changes or modifications derived from the meaning and scope of the claims and their equivalents.

Claims (8)

  1. 약물 주입 장치의 사용 기간에 따른 알림을 제공하는 방법에 있어서,In the method of providing a notification according to the period of use of the drug injection device,
    약물 주입 장치가 비활성 모드(inactive mode)에서 활성 모드(active mode)로 전환되는 시점을 사용 개시 시점으로 결정하는 단계;determining a time when the drug injection device is switched from an inactive mode to an active mode as a start time of use;
    상기 약물 주입 장치의 사용 가능 기간 및 사용자 설정 시간에 기초하여, 상기 사용 개시 시점으로부터 소정의 기간이 지난 제1 시점에 상기 약물 주입 장치의 사용 기간 만료가 임박하였다는 만료 임박 알림을 제공하는 단계; 및based on the usable period of the drug injection device and a user-set time, providing an imminent expiration notification indicating that the expiration date of the use period of the drug injection device is imminent at a first time point when a predetermined period has elapsed from the start of use; and
    상기 사용 개시 시점으로부터 상기 사용 가능 기간이 지난 제2 시점에 상기 약물 주입 장치의 사용 기간이 만료되었다는 만료 알림을 제공하는 단계;providing an expiration notification indicating that the use period of the drug injection device has expired at a second time point when the usable period has elapsed from the start of use;
    를 포함하는, 방법.A method comprising
  2. 제 1 항에 있어서,The method of claim 1,
    상기 방법은,The method is
    상기 제2 시점으로부터 소정의 기간이 지난 제3 시점에 상기 약물 주입 장치가 폐기되어야 한다는 폐기 알림을 제공하는 단계;providing a discard notification that the drug injection device should be discarded at a third time point when a predetermined period has elapsed from the second time point;
    를 더 포함하는, 방법.A method further comprising:
  3. 제 2 항에 있어서,3. The method of claim 2,
    상기 방법은,The method is
    상기 제2 시점과 상기 제3 시점 사이의 제4 시점에 상기 약물 주입 장치의 폐기가 임박하였다는 폐기 임박 알림을 제공하는 단계;providing a discard imminent notification indicating that the disposal of the drug injection device is imminent at a fourth time point between the second time point and the third time point;
    를 더 포함하는, 방법.A method further comprising:
  4. 제 1 항에 있어서,The method of claim 1,
    상기 사용 가능 기간은, The available period is,
    상기 약물 주입 장치로부터 사용자에게 약물이 주입되는 동안, 사용자 인체에 삽입된 상태로 유지되는 대상체의 소재, 상기 소재에 코팅되는 물질 및 구조 중 정 적어도 하나에 기초하여 결정되는 것인, 방법.While the drug is injected from the drug injection device to the user, the method is determined based on at least one of a material of the object maintained in a state inserted into the user's body, a material coated on the material, and a structure.
  5. 제 1 항에 있어서,The method of claim 1,
    상기 사용 가능 기간은, The available period is,
    상기 약물 주입 장치의 저장부 용량 및 하루 평균 투여량에 기초하여 결정되는 것인, 방법.The method of claim 1, wherein it is determined based on the storage capacity of the drug injection device and the average daily dose.
  6. 제 3 항에 있어서,4. The method of claim 3,
    상기 만료 임박 알림, 상기 만료 알림, 상기 폐기 임박 알림 및 상기 폐기 알림을 제공하는 방식은 서로 상이한 것인, 방법.and methods for providing the imminent expiration notification, the expiration notification, the imminent retirement notification, and the revocation notification are different from each other.
  7. 약물 주입 장치의 사용 기간에 따른 알림을 제공하는 장치에 있어서,In the device for providing a notification according to the period of use of the drug injection device,
    적어도 하나의 프로그램이 저장된 메모리; 및a memory in which at least one program is stored; and
    상기 적어도 하나의 프로그램을 실행함으로써 연산을 수행하는 프로세서를 포함하고,A processor for performing an operation by executing the at least one program,
    상기 프로세서는,The processor is
    약물 주입 장치가 비활성 모드에서 활성 모드로 전환되는 시점을 사용 개시 시점으로 결정하고, determining the time when the drug injection device is switched from the inactive mode to the active mode as the starting point of use;
    상기 약물 주입 장치의 사용 가능 기간 및 사용자 설정 시간에 기초하여, 상기 사용 개시 시점으로부터 소정의 기간이 지난 제1 시점에 상기 약물 주입 장치의 사용 기간 만료가 임박하였다는 만료 임박 알림을 제공하고,Based on the usable period of the drug injection device and the user set time, at a first time point when a predetermined period has elapsed from the start of use, an expiration imminent notification indicating that the expiration date of the use period of the drug injection device is imminent;
    상기 사용 개시 시점으로부터 상기 사용 가능 기간이 지난 제2 시점에 상기 약물 주입 장치의 사용 기간이 만료되었다는 만료 알림을 제공하는 것인, 장치.The device, which provides an expiration notification indicating that the use period of the drug injection device has expired at a second time point when the usable period has passed from the start of use.
  8. 약물 주입 장치가 비활성 모드(inactive mode)에서 활성 모드(active mode)로 전환되는 시점을 사용 개시 시점으로 결정하는 단계;determining a time when the drug injection device is switched from an inactive mode to an active mode as a start time of use;
    상기 약물 주입 장치의 사용 가능 기간 및 사용자 설정 시간에 기초하여, 상기 사용 개시 시점으로부터 소정의 기간이 지난 제1 시점에 상기 약물 주입 장치의 교체 임박 알림을 제공하는 단계; 및providing a notification of imminent replacement of the drug injection device at a first time point when a predetermined period has elapsed from the start time of use, based on a usable period of the drug injection device and a user-set time; and
    상기 사용 개시 시점으로부터 상기 사용 가능 기간이 지난 제2 시점에 상기 약물 주입 장치의 사용 기간이 만료되었다는 만료 알림을 제공하는 단계;를 수행하도록 하는 프로그램이 저장된 하나 이상의 컴퓨터로 읽을 수 있는 기록매체를 포함하는 컴퓨터 프로그램 제품.At least one computer-readable recording medium storing a program to perform; providing an expiration notification that the use period of the drug injection device has expired at a second time point when the usable period has passed from the start of use; computer program product.
PCT/KR2021/000317 2020-12-17 2021-01-11 Method, device, and computer program product for providing notification according to period of use of medicine injection device WO2022131436A1 (en)

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Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR100607128B1 (en) * 2003-12-03 2006-08-01 주식회사 우영메디칼 Auto dose infusion control apparatus and method of the same
JP2013188519A (en) * 2008-12-22 2013-09-26 Panasonic Corp Medicament dispensing device
JP2017507703A (en) * 2014-02-05 2017-03-23 バイオエヌテック アーゲーBioNTech AG Cannula, injection or infusion device, and method of using cannula or injection or infusion device
KR20170135362A (en) * 2016-05-31 2017-12-08 주식회사 필로시스 System for automatic management of insulin
KR20200110970A (en) * 2019-03-18 2020-09-28 주식회사 필로시스 Device and method to guide injecting medicine

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR102359279B1 (en) * 2019-06-12 2022-02-08 이오플로우 주식회사 Method for managing disbetes through user terminal

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR100607128B1 (en) * 2003-12-03 2006-08-01 주식회사 우영메디칼 Auto dose infusion control apparatus and method of the same
JP2013188519A (en) * 2008-12-22 2013-09-26 Panasonic Corp Medicament dispensing device
JP2017507703A (en) * 2014-02-05 2017-03-23 バイオエヌテック アーゲーBioNTech AG Cannula, injection or infusion device, and method of using cannula or injection or infusion device
KR20170135362A (en) * 2016-05-31 2017-12-08 주식회사 필로시스 System for automatic management of insulin
KR20200110970A (en) * 2019-03-18 2020-09-28 주식회사 필로시스 Device and method to guide injecting medicine

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