WO2014196068A1 - Dispositif, système et procédé de gestion d'informations de médicament - Google Patents

Dispositif, système et procédé de gestion d'informations de médicament Download PDF

Info

Publication number
WO2014196068A1
WO2014196068A1 PCT/JP2013/065736 JP2013065736W WO2014196068A1 WO 2014196068 A1 WO2014196068 A1 WO 2014196068A1 JP 2013065736 W JP2013065736 W JP 2013065736W WO 2014196068 A1 WO2014196068 A1 WO 2014196068A1
Authority
WO
WIPO (PCT)
Prior art keywords
information
drug
side effect
medicine
registered
Prior art date
Application number
PCT/JP2013/065736
Other languages
English (en)
Japanese (ja)
Inventor
昭二 岩本
智則 望月
Original Assignee
テルモ株式会社
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 テルモ株式会社 filed Critical テルモ株式会社
Priority to PCT/JP2013/065736 priority Critical patent/WO2014196068A1/fr
Publication of WO2014196068A1 publication Critical patent/WO2014196068A1/fr

Links

Images

Classifications

    • G—PHYSICS
    • G16—INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR SPECIFIC APPLICATION FIELDS
    • G16H—HEALTHCARE INFORMATICS, i.e. INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR THE HANDLING OR PROCESSING OF MEDICAL OR HEALTHCARE DATA
    • G16H40/00—ICT specially adapted for the management or administration of healthcare resources or facilities; ICT specially adapted for the management or operation of medical equipment or devices
    • G16H40/60—ICT specially adapted for the management or administration of healthcare resources or facilities; ICT specially adapted for the management or operation of medical equipment or devices for the operation of medical equipment or devices
    • G16H40/63—ICT specially adapted for the management or administration of healthcare resources or facilities; ICT specially adapted for the management or operation of medical equipment or devices for the operation of medical equipment or devices for local operation
    • G—PHYSICS
    • G16—INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR SPECIFIC APPLICATION FIELDS
    • G16H—HEALTHCARE INFORMATICS, i.e. INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR THE HANDLING OR PROCESSING OF MEDICAL OR HEALTHCARE DATA
    • G16H20/00—ICT specially adapted for therapies or health-improving plans, e.g. for handling prescriptions, for steering therapy or for monitoring patient compliance
    • G16H20/10—ICT 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
    • G—PHYSICS
    • G16—INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR SPECIFIC APPLICATION FIELDS
    • G16H—HEALTHCARE INFORMATICS, i.e. INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR THE HANDLING OR PROCESSING OF MEDICAL OR HEALTHCARE DATA
    • G16H70/00—ICT specially adapted for the handling or processing of medical references
    • G16H70/40—ICT specially adapted for the handling or processing of medical references relating to drugs, e.g. their side effects or intended usage

Definitions

  • the present invention relates to a drug information management device, a drug information management system, and a drug information management method, for example, which are held by an individual who takes a drug or the like and manages information such as the drug to be taken.
  • Such a “medicine notebook” is configured by filling medicine information in a paper notebook or pasting a prescription, etc., and as such, there is a problem that it is difficult to handle bulky information.
  • a “medicine notebook using electronic paper” or the like that is stored and stored is proposed (for example, Patent Document 1).
  • the present invention provides a drug information management device, a drug information management system, and a drug information management method that can easily and reliably report side effect information and the like related to a drug of the patient to medical personnel such as a doctor. With the goal.
  • the above object is a drug information management device comprising various information input units that can input various types of information from outside and various information output units that output various types of information, Stores drug information including drug identification information, which is information for specifying a prescribed drug, and drug side effect occurrence information, which is information on occurrence of side effects, as the already registered drug information, and then the various information input unit
  • drug information including drug identification information, which is information for specifying a prescribed drug
  • drug side effect occurrence information which is information on occurrence of side effects
  • the drug information management device has already stored drug information including drug identification information such as a drug name that is information for specifying a prescribed drug and drug side effect occurrence information that is information on occurrence of the side effect. It is stored as registered drug information. After that, when the drug specifying information input from various information input units matches the drug specifying information of the already registered drug information, whether or not the already registered drug information is associated with the drug side effect occurrence information. Are associated with each other, the fact that the drug specifying information is accompanied by drug side effect occurrence information is output to various information output units.
  • drug identification information such as a drug name that is information for specifying a prescribed drug
  • drug side effect occurrence information that is information on occurrence of the side effect. It is stored as registered drug information.
  • the side-effect determination standard information of a specific drug acquires pre-dose biometric information that is patient biometric information before taking the specific drug, and includes patient biometric information after taking the specific drug. It also obtains certain biometric information after taking, determines the presence or absence of side effects related to the specific drug based on the change information of both and the side effect determination criteria information, and when it is determined that a side effect has occurred, the side effect of the drug A feature is that the generation information is generated.
  • the above configuration it is configured to determine whether or not a side effect related to the specific drug has occurred, and to generate drug side effect occurrence information when it is determined that a side effect has occurred. For this reason, even when the patient takes the first medicine, if a side effect occurs by taking the medicine, the fact can be automatically judged and stored. Therefore, the fact that a side effect has occurred can be automatically stored in relation to the drug without the patient or the like operating the drug management device and inputting the information “drug side effect”, so that it is easy to use. It becomes a management device.
  • the side effect determination criterion information is generated based on a specific wording regarding a side effect indicated in the precaution information regarding the drug specifying information input from the various information input units. .
  • the drug information management apparatus can automatically grasp the side effect that occurs for the drug, for example, information such as fever. Therefore, even if the patient refers to the package insert, etc., operates the drug information management device, and does not input the information on the “side effect (fever etc.)” that occurs, the content of the side effect is automatically related to the drug. Therefore, the medicine information management device is easy to use.
  • the potency of the same type of drug is higher than that of the already registered drug information.
  • it is configured to output that the medicinal effect is reduced to the various information output units.
  • medical agent specific information is the same kind drugs, such as a generic drug different from the chemical
  • a medicine information management system comprising: the medicine information management apparatus; and a medical institution side medicine management apparatus arranged to be communicable with the medicine information management apparatus, wherein the medicine information is associated with patient identification information.
  • the identification information and the drug information are transmitted from the drug information management device to the medical institution side drug management device and recorded in an electronic medical record arranged in the medical institution side drug management device.
  • the medicine information stored in the medicine information management apparatus can be automatically stored in the electronic medical record of the medical institution side medicine management apparatus, the medical institution stores the medicine information stored in the medicine information management apparatus.
  • the process of inputting to the medical institution side medicine management apparatus can be omitted. Therefore, the system is easy to use for medical institutions.
  • the drug identification information including the drug identification information for identifying the prescribed drug and the drug side effect occurrence information as the occurrence information of the side effect are registered in the present invention.
  • the drug specifying information input from various information input units that can input various information from the outside coincides with the drug specifying information of the registered drug information. It is determined whether or not the already registered drug information is associated with the drug side effect occurrence information.
  • various information indicating that the drug specifying information is accompanied with the drug side effect occurrence information is displayed. This is achieved by a medicine information management method characterized in that the information is output to various information output units.
  • a drug information management device As described above, according to the present invention, a drug information management device, a drug information management system, and drug information that can easily and reliably report side effect information and the like related to a drug of the patient to medical personnel such as a doctor.
  • a management method can be provided.
  • FIG. 1 is a schematic diagram showing, for example, a medicine notebook management system 1 which is a medicine information management system of the present invention.
  • the medicine notebook management system 1 has, for example, an activity meter 10 which is a medicine information management device.
  • the activity meter 10 has, for example, a three-axis acceleration sensor and the like, and is a device that measures vital data such as intensity of activity and biological information such as total daily calories consumed such as sleep, walk, work, housework, etc. is there.
  • the activity meter 10 since the activity meter 10 is always carried by a user such as a patient due to its nature, not only the total calorie consumption is measured, but also the “drug name” and It has a function of storing drug information such as “side effect information”.
  • “activity meter 10” is shown as a drug information management device that stores drug information and the like.
  • the drug information management device of the present invention is not limited to the activity meter 10, and such information is available. Any medium can be used as long as it can be stored, is convenient for carrying, and has a GUI (Graphical User Interface) function.
  • it may be a portable terminal such as a cellular phone, a data card, a clock, a key, or the like.
  • the activity meter 10 carried by the patient has a thermometer 3, a sphygmomanometer 4, and a blood glucose meter 5 that are always provided in the patient home 2 when the patient is in the patient home 2.
  • the short-range wireless communication is possible on the condition that they are arranged within a certain distance.
  • the activity meter 10 is configured to acquire biometric data such as body temperature, blood pressure value, blood glucose level, and the like from the thermometer 3, blood pressure meter 4 and blood glucose meter 5 by wireless communication.
  • Examples of short-range wireless communication include non-contact communication means for short distances up to about 10 cm (for example, power-saving IC communication technology of ISO / IEC 14443, communication technology of ISO / IEC 18092, FeliCa (Sony Corporation) (Registered trademark)), Bluetooth (registered trademark of Bluetooth SIG), and the like.
  • FeliCa communication technology communication is performed using radio waves of 13.56 MHz, and communication of 100 to 400 kbps is performed in a very close range up to about 10 cm.
  • Bluetooth can communicate at a maximum speed of 24 Mbps using radio waves in the 2.45 GHz band.
  • the activity meter 10 has, for example, activity meter side input devices 11a, 11b, and 11c which are various information input units.
  • the activity meter side input devices 11a, 11b, and 11c are button-like protrusions, switches for inputting signals when pressed, and the like, which are operated by a patient or the like.
  • the activity meter 10 also includes, for example, an activity meter-side communication device 12 that is various information input units capable of short-range wireless communication with an external device or the like.
  • the activity meter 10 includes, for example, an activity meter-side display 13 that is various information output units, and is configured to display various information described later.
  • the medical institution side drug management device For example, the communication with the hospital server 60 is possible. Specifically, as shown in FIG. 1, short-range wireless communication is performed via a “hospital server side read / write device 61” connected to the hospital server 60.
  • the activity meter 10 is connected via the “pharmacy server side read / write device 71”. It has a configuration capable of distance wireless communication.
  • the activity meter 10, the hospital server 60, the pharmacy server 70, the thermometer 3, the sphygmomanometer 4, the blood glucose meter 5 and the like shown in FIG. 1 have computers, and the computer includes a CPU (Central Processing Unit), a RAM (not shown), and a RAM. (Random Access Memory), ROM (Read Only Memory), etc., which are connected via a bus.
  • a CPU Central Processing Unit
  • RAM Random Access Memory
  • ROM Read Only Memory
  • FIG. 2 is a schematic block diagram showing the main configuration of the hospital server 60 of FIG.
  • the hospital server 60 has a hospital server control unit 62.
  • the hospital server control unit 62 stores a hospital server side communication device 63 for communicating with the hospital server side read / write device 61, various data.
  • a hospital server side display 64 to be displayed and a hospital server side input device 65 for inputting various data are controlled.
  • the hospital server control unit 62 also controls a “medicine information storage unit 66”, an “electronic medical record information storage unit 67”, and the like shown in FIG.
  • FIG. 3 is a schematic block diagram showing the main configuration of the activity meter 10 of FIG.
  • the activity meter 10 includes an activity meter control unit 14, and the activity meter control unit 14 includes the activity meter side communication device 12, the activity meter side display 13, and the activity amount.
  • the meter side input devices 11a, 11b11c and the like are controlled.
  • the activity meter control unit 14 also controls the “first various information storage unit 20” and the “second various information storage unit 30” shown in FIG.
  • FIGS. 4 and 5 are schematic block diagrams showing main configurations of the “first various information storage unit 20” and the “second various information storage unit 30” in FIG. 3, respectively. Specific contents thereof will be described later.
  • FIGS. 1 to 5 are schematic flowcharts showing main steps of the medicine notebook management system 1.
  • a patient who is a user of this system always carries the activity meter 10 of FIG. 1 in order to measure his / her activity.
  • the activity meter 10 exhibits the function of the conventional “medicine notebook”, it is always carried when the patient visits the hospital 6 or the pharmacy 7.
  • step ST (hereinafter referred to as “ST”) 1 in FIG.
  • a doctor in charge prescribes a drug to a patient at the hospital 6, and the prescription information is stored in the “drug information storage unit 66” of FIG. 2 together with “patient ID number” that is identification information of the patient.
  • the hospital server 60 is based on the information in the “electronic medical record information storage unit 67”, for example, “pharmaceutical name information” and “attached document information (an example of precautionary note information)” that are drug specifying information of a prescribed drug. Is extracted from the “drug information storage unit 66” and transmitted to the activity meter 10.
  • this transmission is executed via the “hospital server side read / write device 61” in FIG.
  • the “side effect information” eg, fever, blood pressure increase, blood pressure decrease, etc.
  • This “side effect information” is an example of side effect judgment criterion information.
  • the process proceeds to ST2.
  • the “activity meter 10” stores the received “drug information” in the “drug information storage unit 21” of FIG. 4 as “drug information 21a”. That is, the received “attached document” and “side effect information (fever etc.)” are stored in association with the drug name A or the like.
  • the process proceeds to ST3.
  • the “first side effect detection unit (program) 22” in FIG. 4 operates, refers to the “attached document” in the “drug information 21a” in FIG. ”Or“ blood pressure increase ”or the like (an example of specific wording), and after that, it is determined whether or not there is a keyword such as“ possible ”or“ recognized ”.
  • the process then proceeds to ST6.
  • the “second side effect detection unit (program) 23” of FIG. 4 operates, refers to “attached document” of “drug information 21a” of FIG. 4, and includes the wording of “side effect” in the title of “attached document”. It is determined whether there is a keyword such as “fever” or “blood pressure lowering” as side effects in the paragraph below the title.
  • ST6 If a corresponding keyword exists in ST6, the process proceeds to ST7.
  • the corresponding “fever”, “blood pressure reduction”, etc. are stored as “side effect information” in “drug information 21a” in FIG.
  • “side effect information (fever etc.)” stored in “drug information 21a” in FIG. 4 is displayed on the activity meter side display 13 in FIG.
  • side effect information is input in ST3, the process proceeds to ST9.
  • the inputted “side effect information (fever etc.)” is stored in “drug information 21a” of FIG. 4 and the stored “side effect information” is displayed on the activity meter side display 13.
  • the activity meter 10 obtains “side effect information” from the attached document or the like. Since it is automatically extracted, the activity meter 10 is easy to use for patients and the like.
  • the active mass meter 10 determines from the “thermometer 3”, “blood pressure meter 4”, “blood glucose meter 5”, etc. in FIG. 1 to “body temperature information”, “blood pressure information”, “blood glucose level information”, etc. before taking the drug. Is stored in the “pre-medicinal vital information storage unit 24” of FIG. “Pre-drug vital information” such as body temperature information stored in the “pre-medical vital information storage unit 24” is an example of pre-dose biometric information.
  • the process proceeds to ST11.
  • the active mass meter 10 displays on the “active mass meter side display 13” a screen “whether or not a medicine has been taken” and “input name of medicine taken”.
  • the process proceeds to ST12.
  • it is determined whether or not an input of a drug name and a signal indicating that the drug has been taken have been input.
  • the process proceeds to ST13.
  • the active mass meter 10 uses the “medical name information”, “thermometer 3”, “blood pressure meter 4”, “blood glucose meter 5”, etc. taken from the “medical temperature information”, “blood pressure information” and “ The “blood glucose level information” is acquired and stored in the “post-medical vital information storage unit 25” in FIG. 4 as “post-medical vital information”.
  • This post-drug vital information is an example of post-dose biometric information.
  • the process proceeds to ST14.
  • the “side effect occurrence determination unit (program) 26” of FIG. 4 operates, and “pre-medicine vital information” and “post-medical vital information storage unit 25” of the “pre-medicine vital information storage unit 24”. Are compared with each other, and it is determined whether or not the difference is recognized as a side effect of the drug based on the “side effect threshold information” in the “side effect threshold information storage unit 31” in FIG.
  • the side effect threshold information includes specific threshold information in which “body temperature”, “blood pressure increase”, “blood pressure decrease” and the like are recognized as side effects.
  • the process proceeds to ST15.
  • the process proceeds to ST16.
  • the activity meter 10 stores the drug as “provisional side effect drug” in “drug information 21a” of the “drug information storage unit 21” in FIG. I have a higher body temperature. It may have caused side effects.
  • This “provisional side effect drug” information is an example of drug side effect occurrence information.
  • the activity meter 10 automatically determines that a side effect may have occurred in the medicine taken by the patient carrying the activity meter 10 and stores the fact. .
  • the device since it is not necessary for the patient to input the occurrence of a side effect, the device is easy to use.
  • the process proceeds to ST17.
  • the occurrence of a side effect is a tentative provisional determination, and therefore, in ST17 and subsequent steps, a process for seeking a determination by a doctor in charge is requested.
  • the doctor in charge or the like determines the data determined by the activity meter 10 as “provisional side effect drug” and similarly determines that it is “side effect”, and waits for the “confirmation signal” from the hospital server 60. It is a process. Specifically, this is a case where the patient carries his / her active mass meter 10, goes to the hospital for medical examination, and shows the “side effect” data to the doctor in charge. When the doctor in charge who sees this data determines that it is a side effect, a “confirmation signal” is input directly or via the hospital server 60.
  • a “confirmation signal”, that is, a “confirmed side effect drug” signal is input in ST17, the process proceeds to ST18.
  • the drug in the “drug information storage unit 21” is stored as a “confirmed side effect drug”. Therefore, this confirms that the drug is a “side effect drug” that caused side effects for the patient.
  • the occurrence of a side effect is temporarily estimated and notified to a patient or the like, but since the decision information is awaited by a specialist doctor or the like, the decision information is highly reliable information. It has become.
  • the “determined side effect drug” is also an example of drug side effect occurrence information.
  • the process proceeds to ST19.
  • the “activity meter 10” transmits the “confirmed side effect information” of the drug information 21a to the hospital server 60, and the hospital server 60 stores it in the “electronic medical record information storage unit 67” of FIG. Therefore, the latest side effect information of the patient is automatically reflected in the “electronic medical record” of the hospital, and the doctor in charge or the like can always make an accurate judgment when selecting the medicine.
  • the process proceeds to ST20.
  • ST20 it is determined whether or not there is a cancellation signal of “provisional side effect drug” in the drug information 21a from the hospital server 60 or a doctor in charge directly. If there is a cancel signal, the process proceeds to ST21.
  • ST21 since no side effect has occurred in the drug, the information of “provisional side effect drug” of the drug in the drug information storage unit 21 is deleted. In this way, in this embodiment, information that is not supported by the doctor in charge is quickly deleted, and it is possible to prevent misunderstandings and the like from occurring in patients and the like.
  • FIG. 9 is a schematic flowchart showing an operation example when a patient carries his / her own activity meter 10 and receives a medical examination by a doctor who does not regularly visit, that is, when he / she visits a travel destination. is there.
  • a patient or the like who sees a doctor or the like shows his / her activity meter 10 to the doctor or the like.
  • doctors and the like operate the activity meter 10 shown in FIG. 1 and input a request for viewing “drug information 21a” in order to know what drugs the patient takes and side effects. To do.
  • ST31 when there is an input of a request for viewing “medicine information 21a”, the process proceeds to ST32.
  • the “ordinary side effect drug” or “determined side effect drug” is stored in the “medicine information 21a” of FIG. Is displayed on the activity meter side display 13 as a “side effect drug”. Further, “medicine” that is not “provisional side effect drug” or “confirmed side effect drug” is displayed as “ordinary drug”.
  • FIGS. 12 and 13 are schematic diagrams illustrating an operation example and a display example of the activity meter 10.
  • the doctor or the like can use, for example, the switch 11c of the activity meter side input device 11c. Press.
  • FIG. 12A a list of drug names classified into the above-mentioned “ordinary drugs” in the “drug information 21a” is displayed on the activity meter side display 13.
  • the activity meter side input devices 11a and 11b of FIG. 12A are operated, the screen scrolls up and down, and all “normal medicines” can be easily visually recognized.
  • doctors and the like can obtain necessary information, for example, names of side effect drugs and details of side effects, quickly and accurately by a simple operation.
  • ST33 “medicine information” related to the prescription is transmitted to the activity meter 10 from the hospital-side read / write device 61 of the hospital server 60 of the hospital 6 where the patient is consulting.
  • drug information or the like is transmitted from the pharmacy read / write device 71 of the pharmacy server 70 of the pharmacy 7 to the activity meter 10.
  • the process proceeds to ST34.
  • the “activity meter 10” stores the received “drug information” in the “drug information storage unit 21” of FIG.
  • the process proceeds to ST35.
  • the “side effect drug corresponding determination unit (program) 33” in FIG. 5 operates, and it is determined whether or not the input “drug name” matches “side effect drug” in “drug information 21a” in FIG. to decide.
  • the process proceeds to ST42.
  • the “activity meter 10” stores the received “drug information” in the “drug information storage unit 21” of FIG.
  • the process proceeds to ST43.
  • ST43 it is determined whether or not the input “drug name” is a new drug name, that is, the same as the drug name stored in “drug information 21a” in FIG.
  • the process proceeds to ST44.
  • ST44 it is determined whether or not the new drug name is a generic drug of the same type as the drug name registered in the “medicine information 21a” of FIG. If it is determined in ST44 that the drug is a generic drug, the process proceeds to ST45.
  • the activity meter 10 acquires “body temperature information”, “blood pressure information”, and “blood glucose level information” before taking the drug from the “thermometer”, “blood pressure meter”, “blood glucose meter”, etc. Stored in the “pre-medicine vital information storage unit 24”.
  • Step 46 “whether or not a new medicine has been taken” and “input of the name of a new medicine taken” screen are displayed on the “activity meter side display 13”.
  • ST47 it is determined whether or not a signal indicating that a new medicine has been taken has been input. If it has been input, the process proceeds to ST48.
  • the active mass meter 10 uses the “medicine name information”, “thermometer”, “blood pressure meter”, “blood glucose meter”, etc. taken from the “medical temperature information”, “blood pressure information” and “blood glucose level information” after taking the drug. Is acquired and stored in the “post-medical vital information storage unit 25” in FIG.
  • ST49 the “medicine efficacy comparison / determination unit (program) 34” of FIG. 5 operates, and the “pre-medicine vital information storage unit 24” and the “pre-medicinal vital information storage unit 24” Compare the “post-drug vital information”, obtain the difference, and refer to the “regular drug efficacy information storage unit 35” in FIG. 5 to determine whether the drug efficacy is inferior to that of the same type of drug. to decide.
  • the “regular drug efficacy information storage unit 35” stores past drug efficacy information of a drug corresponding to the same type of drug stored as “drug information”. For example, in the case of an antihypertensive agent, information about a decrease in blood pressure is stored. Therefore, “regular drug efficacy information” is an example of drug efficacy information of already registered drug information.
  • ST50 If it is determined in ST50 that the generic drug is inferior to the existing “normal drug”, the process proceeds to ST51.
  • ST 51 “Warning: Drug efficacy has been reduced by changing the normal medicine” is displayed on the activity meter side display 13.
  • SYMBOLS 1 Medicine notebook management system, 2 ... Patient home, 3 ... Thermometer, 4 ... Blood pressure meter, 5 ... Blood glucose meter, 6 ... Hospital, 7 ... Pharmacy, 10 ... Activity meter, 11a, 11b, 11c ... Activity meter side input device, 12 ... Activity meter side communication device, 13 ... Activity meter side display, 14 ... Activity meter Control part, 20 ... 1st various information storage part, 21 ... Drug information storage part, 21a ... Drug information, 22 ... 1st side effect detection part (program), 23 ... 2nd side effect Discovery unit (program), 24 ... pre-drug vital information storage unit, 25 ... post-drug vital information storage unit, 26 ...
  • side effect occurrence determination unit program
  • 30 second type Information storage unit
  • 31 Side effect threshold information storage unit
  • 32 (Program)
  • 33 ... side effect medicine corresponding judgment part (program)
  • 34 ... medicinal efficacy comparison judgment part (program)
  • 35 ... regular medicine medicinal information storage part, 60 ... hospital server, 61 ... Hospital server side read / write device, 70 ... pharmacy server, 71 ... pharmacy server side read / write device

Landscapes

  • Engineering & Computer Science (AREA)
  • Health & Medical Sciences (AREA)
  • Medical Informatics (AREA)
  • Public Health (AREA)
  • Primary Health Care (AREA)
  • Epidemiology (AREA)
  • General Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Chemical & Material Sciences (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Biomedical Technology (AREA)
  • General Business, Economics & Management (AREA)
  • Business, Economics & Management (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Toxicology (AREA)
  • Medical Treatment And Welfare Office Work (AREA)

Abstract

Le problème décrit par la présente invention est de fournir un dispositif de gestion d'informations de médicament, etc., selon lequel il est possible d'avertir de manière facile et fiable des praticiens médicaux, etc., tels que des médecins, d'informations d'effet secondaire, etc., se rapportant à un médicament d'un patient. La solution selon l'invention consiste en un dispositif (10) de gestion d'informations de médicament, qui comprend des unités d'entrée pour diverses informations (11a, 11b, 11c) qui sont susceptibles de recevoir une entrée de diverses informations depuis une source externe, et une unité de sortie pour diverses informations (13) qui produit diverses informations. Les informations (21a) de médicament sont mémorisées sous la forme d'informations de médicament préenregistrées, comprenant au moins des informations de spécification du médicament qui sont des informations permettant de spécifier un médicament prescrit et des informations de survenue d'effets secondaires de médicament, qui sont des informations concernant la survenue d'un effet secondaire de celui-ci. Lorsque des informations de spécification de médicament qui sont entrées par la suite par l'intermédiaire des unités d'entrée pour diverses informations correspondent aux informations de spécification de médicament des informations de médicament préenregistrées, une détermination est faite concernant la liaison ou non des informations de médicament préenregistrées aux informations de survenue d'effets secondaires de médicament et, si elles sont liées, les informations selon lesquelles les informations de spécification de médicament possèdent les informations de survenue d'effets secondaires de médicament associées à celles-ci sont envoyées à l'unité de sortie pour diverses informations.
PCT/JP2013/065736 2013-06-06 2013-06-06 Dispositif, système et procédé de gestion d'informations de médicament WO2014196068A1 (fr)

Priority Applications (1)

Application Number Priority Date Filing Date Title
PCT/JP2013/065736 WO2014196068A1 (fr) 2013-06-06 2013-06-06 Dispositif, système et procédé de gestion d'informations de médicament

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
PCT/JP2013/065736 WO2014196068A1 (fr) 2013-06-06 2013-06-06 Dispositif, système et procédé de gestion d'informations de médicament

Publications (1)

Publication Number Publication Date
WO2014196068A1 true WO2014196068A1 (fr) 2014-12-11

Family

ID=52007740

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/JP2013/065736 WO2014196068A1 (fr) 2013-06-06 2013-06-06 Dispositif, système et procédé de gestion d'informations de médicament

Country Status (1)

Country Link
WO (1) WO2014196068A1 (fr)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2019128665A (ja) * 2018-01-22 2019-08-01 株式会社富士通アドバンストエンジニアリング 服薬支援プログラム、装置、及び方法
JP2021047821A (ja) * 2019-09-20 2021-03-25 株式会社Ｗｉｎｄｙ 調剤薬局側システムに蓄積された患者服薬関連情報を活用した医師診療支援システム及び方法

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2005100454A (ja) * 2004-11-18 2005-04-14 Mitsui Sumitomo Insurance Co Ltd 健康情報管理サーバ及びプログラム
JP2005266853A (ja) * 2004-03-16 2005-09-29 Nec Corp 薬情報管理端末、薬情報管理システムおよび薬情報管理プログラム
JP2007188149A (ja) * 2006-01-11 2007-07-26 Sharp Corp 服薬情報提供システム、服薬情報提供サーバ、服用者端末、並びにプログラムおよび記録媒体
JP2010009536A (ja) * 2008-06-30 2010-01-14 Higashi Nihon Medicom Kk 調剤システム
JP2010218439A (ja) * 2009-03-18 2010-09-30 Fujitsu Ltd 処方オーダ発行プログラム、処方オーダ発行装置及び方法

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2005266853A (ja) * 2004-03-16 2005-09-29 Nec Corp 薬情報管理端末、薬情報管理システムおよび薬情報管理プログラム
JP2005100454A (ja) * 2004-11-18 2005-04-14 Mitsui Sumitomo Insurance Co Ltd 健康情報管理サーバ及びプログラム
JP2007188149A (ja) * 2006-01-11 2007-07-26 Sharp Corp 服薬情報提供システム、服薬情報提供サーバ、服用者端末、並びにプログラムおよび記録媒体
JP2010009536A (ja) * 2008-06-30 2010-01-14 Higashi Nihon Medicom Kk 調剤システム
JP2010218439A (ja) * 2009-03-18 2010-09-30 Fujitsu Ltd 処方オーダ発行プログラム、処方オーダ発行装置及び方法

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2019128665A (ja) * 2018-01-22 2019-08-01 株式会社富士通アドバンストエンジニアリング 服薬支援プログラム、装置、及び方法
JP2021047821A (ja) * 2019-09-20 2021-03-25 株式会社Ｗｉｎｄｙ 調剤薬局側システムに蓄積された患者服薬関連情報を活用した医師診療支援システム及び方法

Similar Documents

Publication Publication Date Title
Bhardwaj et al. IoT-based smart health monitoring system for COVID-19
Nedungadi et al. Personalized health monitoring system for managing well-being in rural areas
KR101903407B1 (ko) 원격 건강 관리 솔루션에서 비디오를 기반으로 한 헬스 케어 시스템 및 헬스 케어 서비스 제공방법
Latif et al. I-CARES: advancing health diagnosis and medication through IoT
US20160377592A1 (en) Single-use handheld diagnostic test device, and an associated system and method for testing biological and environmental test samples
KR100914633B1 (ko) 환자 맞춤형 건강관리 시스템 및 그 방법
TW587929B (en) Medical checkup network system
US20070027367A1 (en) Mobile, personal, and non-intrusive health monitoring and analysis system
US20100169220A1 (en) Wearing health on your sleeve
US20140081087A1 (en) Mobile device system actively capturing physiological parameters
KR20060124082A (ko) 건강 측정 장치 및 그를 이용한 건강 관리 방법 및 그시스템
US20140310024A1 (en) Wifi cloud electronic vital-sign monitoring system
KR20140053142A (ko) 건강관리 동기부여를 위한 자가 인지 리마인더를 제공하는 헬스 케어 서비스 제공방법
KR20010095395A (ko) 원격 건강 관리 시스템 및 이 시스템용 각종 개인 건강정보 측정용 단말기
KR20090065869A (ko) 생체 신호 검출을 기반으로 하는 건강 관리 서비스 시스템및 이의 모니터링 방법
TWI668664B (zh) Method for dynamically analyzing blood sugar level, system thereof and computer program product
JPWO2014119575A1 (ja) 管理装置、管理システム及び管理方法
WO2014196068A1 (fr) Dispositif, système et procédé de gestion d'informations de médicament
JP2007286947A (ja) 健康維持管理システム
KR20140062659A (ko) 헬스아바타를 이용한 ｕ-헬스케어 시스템 및 ｕ-헬스케어 정보 제공 방법
Briggs et al. M-health review: joining up healthcare in a wireless world
Isravel et al. A novel framework for quality care in assisting chronically impaired patients with ubiquitous computing and ambient intelligence technologies
US11317290B2 (en) Information processing apparatus, server, and data transmission system
JP2006048670A (ja) 医療情報処理システム、医療情報処理用記憶媒体および医療情報処理用読取装置
Ulle Challenges and Opportunities for IoT Deployment in India’s Healthcare Sector

Legal Events

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

Ref document number: 13886488

Country of ref document: EP

Kind code of ref document: A1

NENP Non-entry into the national phase

Ref country code: DE

122 Ep: pct application non-entry in european phase

Ref document number: 13886488

Country of ref document: EP

Kind code of ref document: A1

NENP Non-entry into the national phase

Ref country code: JP