WO2014162486A1 - Medical-information management device and medical-information management method - Google Patents

Abstract

[Problem] To provide a medical-information management device or the like which is capable of automatically changing whether or not to provide a display or the like of a "clinical advisory," which is information such as a "warning" pertaining to drug information, according to the frequency at which such an alert occurs. [Solution] A medical-information management device (10) for providing drug information to a medical device (70a), the medical-information management device (10) being configured so as to be capable of associating and providing warning information pertaining to the drug information when providing said drug information, and being configured so as to determine whether the provision of warning information is necessary or not on the basis of occurrence-frequency information (77a) for the alert information for actual occurrences pertaining to said drug.

Description

Medical information management apparatus and medical information management method

The present invention relates to a medical information management apparatus and a medical information management method for managing medical information such as drug information used in hospitals, for example.

Conventionally, in hospitals and the like, infusion pumps and the like have been used in order to appropriately administer drugs to patients (for example, Patent Document 1).
In recent years, such infusion pumps and the like have a high function of holding and using drug information. Moreover, in such an infusion pump, when the said drug tends to generate | occur | produce various errors in the past about the chemical | medical agent which the said pump delivers, etc., the fact is alert | reported to the user of the said infusion pump, and attention is drawn. The “clinical advisory” function is also available.
Specifically, information on “attention” is displayed in association with the medicine displayed on the display of the infusion pump.

JP 2011-87678 A

However, depending on the medicine, as the use proceeds, the occurrence of alerts such as various errors has already been reduced, and the above-mentioned “warning” display may be unnecessary. However, once the alert information is registered, the alert pump is always displayed on the display such as the infusion pump in relation to the drug. To change the display, re-register it. Etc. are required, forcing the user to perform complicated operations.
On the other hand, after a complicated operation and changing registration, many alerts such as errors are generated again, and it may be necessary to change again.

Accordingly, the present invention provides medical information that can automatically change whether or not to provide a display such as “Clinical Advisory” that is information such as “Awareness” related to drug information, depending on the frequency of occurrence of the alert, etc. An object is to provide a management apparatus and a medical information management method.

In the present invention, the object is a medical information management device that provides drug information to a medical device, and can provide alert information related to the drug information in association with the drug information when the drug information is provided. In addition, the provision of the alert information is configured to determine whether or not the provision of the alert information is necessary based on the occurrence frequency information of the actually generated warning information regarding the drug. Achieved by the device.

According to the said structure, provision of alerting | reporting information becomes a structure by which the necessity is judged about the said chemical | medical agent based on the frequency information of the warning information which generate | occur | produced actually.
For this reason, when the use of medicine progresses, the occurrence of alerts such as various errors has already been reduced, and the provision of “warning information” is unnecessary, the provision is automatically stopped.
Thereafter, when the occurrence of alarms such as various errors increases again, provision of “warning information” is automatically started.
Therefore, it is an easy-to-use medical information management apparatus that does not require the user to perform complicated operations such as registration and change as to whether or not the “warning information” needs to be provided.

Preferably, the necessity of providing the alert information is determined based on occurrence frequency information of the warning information generated in the medical device.

According to the above configuration, since it is determined whether or not it is necessary to provide the alert information based on the frequency information of the warning information generated in the medical device, the generation of warning information such as an alert in the medical device is generated. Based on the frequency, it is possible to determine whether or not it is necessary to provide “warning information”.

Preferably, the occurrence frequency information of the warning information includes time zone information of the occurrence, and the alert information is provided to the medical device when the warning information corresponds to time zone information having a high occurrence frequency of the warning information. It is the structure.

According to the above configuration, since the alert information is provided to the medical device when it corresponds to the time zone information with a high occurrence frequency of the alert information, it is possible to provide detailed “notice information”.

Preferably, the occurrence frequency information of the warning information is collected for each medical device, and the alert information is provided to the medical device having a high occurrence frequency. .

According to the above configuration, the occurrence frequency information of the warning information is collected for each medical device, and the alert information is provided to the medical device with the high occurrence frequency, so it is provided to the detailed “attention information” Is possible.

In the present invention, the object is a medical information management method for providing drug information to a medical device, and can be provided in association with alert information relating to the drug information when the drug information is provided. In addition, the provision of the alert information is configured to determine whether or not the provision of the alert information is necessary based on the occurrence frequency information of the warning information that has actually occurred. Achieved by management method.

As described above, according to the present invention, the presence / absence of display of “clinical advisory” or the like, which is information such as “attention” regarding drug information, is automatically determined based on the occurrence frequency of the alert or the like. It is possible to provide a medical information management device and a medical information management method that can be changed to

It is the schematic which shows the "medicine library system" provided with the "medicine library server" which is the "medical information management apparatus" of this invention, for example. It is a schematic block diagram which shows the infusion pump shown in FIG. It is a schematic block diagram which shows the chemical | medical agent library server shown in FIG. It is a schematic block diagram which shows the content of the "1st various information storage part" of FIG. It is a schematic block diagram which shows the content of the "2nd various information storage part" of FIG. It is a schematic block diagram which shows the content of the "3rd various information storage part" of FIG. 3 is a schematic flowchart showing a main operation example of the “drug library system” shown in FIG. 1. 7 is another schematic flowchart showing a main operation example of the “drug library system” shown in FIG. 1. 7 is another schematic flowchart showing a main operation example of the “drug library system” shown in FIG. 1. 7 is another schematic flowchart showing a main operation example of the “drug library system” shown in FIG. 1. 7 is another schematic flowchart showing a main operation example of the “drug library system” shown in FIG. 1.

Preferred embodiments of the present invention will be described below in detail with reference to the accompanying drawings.
The embodiments described below are preferred specific examples of the present invention, and thus various technically preferable limitations are given. However, the scope of the present invention is particularly limited in the following description. Unless otherwise stated, the present invention is not limited to these embodiments.

FIG. 1 is a schematic diagram showing a “medicine library system 1” including a “medicine library server 10”, which is a “medical information management apparatus” of the present invention.
As shown in FIG. 1, the “drug library system 1” has a “medical device”, for example, an “infusion pump 70a”, in addition to the “drug library server 10” that stores various information related to drugs. These are communicably connected.

These infusion pumps 70a and the like are for administering the drug A and the like to the patient. That is, the infusion pump 70a and the like have a configuration in which a tube (not shown) that feeds a drug solution such as the drug A can be disposed therein, and performs operations such as pressing by pressing the tube. Thus, the flow rate of the chemical solution fed in the tube is controlled.

In addition, the infusion pump 70a and the like have, for example, an “infusion pump side display 71” that is a display unit that displays various information, and also an “infusion pump side input device 72” that is an input unit that inputs various information. ing.
Specifically, the “infusion pump side input device 72” is a dial, an input button, or the like.

When a drug is administered to a patient using such an infusion pump 70a or the like, the infusion pump displays “medicine library”, which is drug information transmitted from the drug library server 10, on the infusion pump side display 71. The
Therefore, the medical staff such as a nurse who operates can easily and definitely administer the medicine.
In the present embodiment, the “drug library” displayed on the “infusion pump-side display 71” includes not only information such as “soft limit” that is restriction information such as prescription of the drug itself, but also at the time of administration. The “warning information (clinical advisory information)” that alerts the user is displayed as necessary. Details will be described later.

Incidentally, the infusion pump 70a and the like and the drug library server 10 shown in FIG. 1 have a computer, and the computer has a CPU (Central Processing Unit), a RAM (Random Access Memory), a ROM (Read Only Memory), and the like (not shown). These are connected via a bus.

FIG. 2 is a schematic block diagram showing the infusion pump 70a and the like shown in FIG.
As shown in FIG. 2, the infusion pump 70 a and the like have an “infusion pump control unit 73”. The infusion pump control unit 73 controls the “infusion pump side input device 72” and the “infusion pump side display 71” shown in FIG. 1, and communicates with the “medicine library server 10” in FIG. The “infusion pump main body 75” that performs the original operation of the “pump-side communication device 74”, the infusion pump 70a, and the like is controlled. Further, the “infusion pump control unit 73” is, for example, “alert signal generator 76” or “pump side alert” that generates “alert” that is “warning information” when an error or the like occurs in the infusion pump 70a or the like. The information storage unit 77 "and the like are also controlled.
The alert includes, for example, “soft limit” exceeding the restriction information on the administration of medicines, “hard limit” conflicting that is the absolute administration range information on the administration of medicines, and the like.
The contents of the “pump-side alert information storage unit 77” will be described later.

FIG. 3 is a schematic block diagram showing the drug library server 10 shown in FIG.
As illustrated in FIG. 3, the drug library server 10 includes a “server control unit 11”. The “server control unit 11” includes a “server-side input device 12” that inputs various information, a “server-side display 13” that displays various information, and the “server-side communication device 14” that communicates with the infusion pump 70a of FIG. And the “first various storage units 20”, “second various storage units 30”, and “third various storage units 40” shown in FIG.
4 to 6 are schematic block diagrams showing the contents of “first various information storage unit 20”, “second various information storage unit 30”, and “third various information storage unit 40” in FIG. 3, respectively. . These contents will be described later.

7 to 11 are schematic flowcharts showing main operation examples of the “drug library system 1” shown in FIG. Hereinafter, the operation and the like will be described according to the flowcharts of FIGS. 7 to 11, and the configuration and the like of FIGS. 1 to 6 will be described.

First, using FIG. 7 and FIG. 8, whether or not the infusion pump 70a of FIG. 1 has issued an alert signal during administration of a specific medicine A, etc., and whether the frequency of the alert signal is high. The process of determining will be described.

First, in step ST (hereinafter referred to as “ST”) 1 in FIG. 7, the infusion pump 70 a and the like in FIG. 1 is medicine information such as medicine A displayed on the “infusion pump side display 71”. The “medicine library” is displayed, and the liquid feeding operation of the specific medicine A is executed.

Next, the process proceeds to ST2. In ST2, it is determined whether or not an alert signal is issued by the “alert signal generator 76” of FIG. 2 such as the infusion pump 70a during the liquid feeding operation.
Specifically, the soft limit excess, hard limit conflict, etc. of the drug.

When an “alert signal” is issued in ST2, the process proceeds to ST3. In ST3, the pump number of the infusion pump 70a (for example, 70a), the date and time when the alert occurred, the alert content (for example, soft limit exceeded, etc.), the medicine name (A), etc. are shown in “Pump-side alert information storage unit 77” in FIG. Is stored as “pump side alert information 77a”.
This “pump-side alert information 77a” is an example of “occurrence frequency information”.

Then proceed to ST4. In ST4, the infusion pump 70a and the like transmit “pump-side alert information” in the “pump-side alert information storage unit 77” in FIG. 2 to the drug library server 10 via the “infusion pump-side communication device 74”.

Next, proceed to ST5. In ST5, the drug library server 10 stores the received “pump-side alert information” as “server-side alert information 21a” of the “server-side alert information storage unit 21” in FIG.

Next, the process proceeds to ST6. In ST6, the “alert occurrence level determination unit (program) 22” of FIG. 4 operates and refers to the “server side alert information storage unit 21” and “alert occurrence level reference information storage unit 23” of FIG.
In the “alert occurrence level reference information storage unit 23”, the following reference information is stored.
1) Reference information on the level of alert generation for each infusion pump 70a and the like (information on how much the infusion pump 70a etc. determines to be “high” when an alert is issued in one month).
2) Standard information on the level of occurrence of general alerts by month for each drug (information on how much it is determined to be “high” when an alert is issued per month for each drug A, etc.).
3) How often an alert is issued per month for each drug and every time period (6 o'clock to 12 o'clock, etc.) Information).

Then, the number of alerts per month for the drug is calculated from the information on the number of alerts accumulated in the “server-side alert information 21a” in FIG. 4 and the occurrence date / time information, and the number of alerts and “alert occurrence level reference information storage” are calculated. Section 23 "is compared with the monthly general alert occurrence level reference information for each drug, and" alert occurrence level information "of" general alert occurrence count / month "is generated, with" alert occurrence level information "in FIG. It is stored as a part of the “medicine library 24a with alert occurrence height information” in the “medicine library storage unit 24”.
Specifically, it is stored as “high / low” information of “general alert occurrence count / month” in “drug library with alert occurrence height information 24a”.

In the present embodiment, in the “drug library 24a with alert occurrence level information” in FIG. 4, the drug name A is determined based on the criteria of the “alert occurrence level reference information storage unit 23” for the number of alerts per month. , “High (alert frequency is high)”.

In ST6, since the alert time information accumulated in the “server-side alert information 21a” in FIG. 4 and the occurrence date and time information thereof can be grasped, the alert occurrence time zone information can be obtained. The time zone information in the drug library with high and low information 24a is, for example, “number of alerts generated from 6:00 to 12: 00 / month”, “number of alerts generated from 12:00 to 18: 00 / month” and “18:00 to The number of occurrences of the alert for each “24 o'clock alert occurrence / month” is calculated and stored.
Then, the number of occurrences / month of alerts for each time period and the “reference information for alert occurrence level for each time of each drug” in the “alert occurrence level reference information storage unit 23” are compared, and “high / low” is determined. And remember.
For example, in the example of FIG. 4, since the “number of occurrences of alerts from 6 o'clock to 12 o'clock / month” of drug B is “high”, drug B has a high occurrence of alerts during this time period. .

As shown in FIG. 4, the “drug library with alert occurrence height information” 24a includes information on the above-mentioned alert in the drug information (soft limit information, etc.) of the drug library for each drug A, B, and C. In addition to being associated with each other, color information such as “red” is also associated with the difference in efficacy and utility of each drug.
Therefore, when the drug information is displayed on the “infusion pump side display 71” such as the infusion pump 70a, the color information such as red is also displayed.

This color information indicates the degree to which the drug has a strong effect and effect and requires attention for administration. For example, “red” is a group of drugs that require the most attention.
Therefore, when a nurse or the like refers to the drug library information on the “infusion pump side display 71” such as the infusion pump 70a, the color information such as red is also visually recognized at the same time. It is configured so that it can be easily grasped whether to pay.

Next, the process proceeds to ST7. In ST7, the “alert occurrence level determination unit (program) 22” of FIG. 4 operates, and refers to the pump number (70a etc.) and “alert occurrence date / time information” of “server side alert information 21a” of FIG. The number of alert occurrences / month for each infusion pump 70a is calculated. Then, “high / low” is determined by comparing with “reference information of alert generation high / low for each infusion pump 70a” in “alert generation high / low standard information storage unit 23” of FIG.
Thereafter, “per-pump alert occurrence height information 31a” of FIG. 5 is generated and stored in the “pump alert occurrence height information storage unit 31” in association with the “high / low” information together with the “pump number” information and the number of alert occurrences / month.

In the above process, the “drug library 24a with alert occurrence level information” in FIG. 4 stores “high” or “low” information of the alert occurrence frequency for each drug, and the alert for each time zone of each drug. Information on “high” or “low” occurrence frequency is stored.
In addition, “high / low” information on the alert occurrence frequency for each pump number of the infusion pump 70a and the like is stored in ““ Alert occurrence level information 31a for each pump ”in FIG.

Based on these information, in the next step, when the drug library is displayed on the “infusion pump side display 71” such as the infusion pump 70a, it is determined whether or not the “warning” information is displayed at the same time. Become.

By the way, after ST7, the process proceeds to ST8 in FIG. 8, and it is determined whether or not the liquid feeding operation of the infusion pump 70a and the like is completed.

Next, display / non-display of the “calling attention” information will be described in detail with reference to FIGS. 9 to 11.
First, in ST11 in FIG. 9, the “communicable pump identification unit (program) 32” in FIG. 5 operates and an infusion pump number (identification information) such as the infusion pump 70a that can communicate with the drug library server 10 in FIG. For example, 70a and the like are stored in the “communicable infusion pump information storage unit 32” as “communicable infusion pump information” in FIG.

Then, before sending the drug information such as the drug library to the infusion pump 70a or the like, it is determined whether or not “warning” information is displayed on the “infusion pump side display 71” in the following steps.
That is, in ST12, the “first alert information display availability determination unit (program) 34” operates and refers to the “high / low” information of “general alert occurrence count / month” in the “drug library with alert occurrence height information 24a”. To do. As the “high / low” information, the high / low information is set to “high” when, for example, XX% is higher than the average of “general alert occurrence count / month”. Preferably, the “high” information is automatically updated every week or every month.

Next, the process proceeds to ST13. In ST13, it is determined whether or not the high / low information of “general alert occurrence count / month” in “drug library with alert occurrence height information 24a” is “high”.
In ST13, when there is a drug name whose height information is “high”, for example, A, the process proceeds to ST14.
In ST14, the drug name (for example, A) whose level information is “high” is associated with “warning information” as the alert frequency is high and attention should be paid, and the “medical drug with first attention information” in FIG. Library information 35a "is generated and stored in" drug library information storage unit 35 with first alert information ".

On the other hand, in ST13, when there is no drug name having high / low information of “high”, the process proceeds to ST15.
In ST15, “drug library information 35b with first alert information” shown in FIG. 5 is generated without associating the drug name A and the like with “notice information”, and “drug library information storage unit with first alert information” is generated. 35 ".

Next, proceed to ST16. In ST16, the “second alerting information display availability determination unit (program) 41” in FIG. 6 operates, and “6-12 o'clock occurrence count / month” in the “drug library with alert occurrence level information” in FIG. Refer to the "high and low" information of the time zone information.

Then, in ST17, it is determined whether or not there is time zone information such as “6-12 o'clock occurrence count / month” where the height information is “high”.
In ST17, when there is time zone information whose height information is “high”, for example, in the “drug library with alert occurrence height information 24a” in FIG. The time zone information of is “high” and exists.

In this case, the “warning information” is associated with the drug name B having “time zone information” such as “6-10 o'clock occurrence count / month” whose height information is “high”, Such information is added to the “drug library information 35a, 35b” to generate “drug library information 35a-a, 35b-a with second alert information” in FIG. 6, and “drug library information with second alert information”. The data is stored in the storage unit 42 ”as shown in FIG.

That is, “drug library information 35a-a with second alert information” in FIG. 6 adds “attention information” of “time zone information” to “drug library information 35a with first alert information” in FIG. It is a thing. Further, “drug library information 35b-a with second alert information” is obtained by adding “notice information” of “time zone information” to “drug library information 35b with first alert information” in FIG. is there.

On the other hand, if it is determined in ST17 that there is no “high” time zone information of the height information, the process proceeds to ST19. In ST19, the “drug library information 35a, 35b with first alert information” in FIG. 5 is not associated with the “notice information” in the time zone information, and the “drug library information 35a with second alert information” in FIG. -B, 35b-b "is generated and stored in the" drug library information storage unit 42 with second alert information ".

As described above, the information of “drug library information 35a-a, 35b-a, 35a-b, 35b-b with second alert information” in FIG. 6 is “drug library 24a with alert occurrence height information” in FIG. The “general alert occurrence count / month” “high / low” information and “6-10 o'clock occurrence count / month” etc. “time zone information” “high / low” information are combined as examples.

Next, proceed to ST20. In ST20, the “third alerting information display availability determination unit (program) 43” of FIG. 6 operates, and the “per-pump alert occurrence level information storage unit 31” of FIG. Refer to “High / Low” information.

Next, proceed to ST21. In ST21, it is determined whether or not “high” “pump number” is included in the high and low information of “per-pump alert occurrence height information 31a” in FIG.

If it is determined in ST21 that the “pump number” of “high” is included in the height information of “alert pump height information 31a” of FIG. 5, the process proceeds to ST22.
In ST22, “warning information” is associated with “pump number (for example, 70c)” whose height information is “high”. Then, with reference to the “library 24a with alert occurrence height information” in FIG. 4, “drug library information with third alert information 44a” as shown in FIG. 6 is generated, and “drug library with third alert information” It memorize | stores in the information storage part 44 ".

The “drug library information 44a with third alerting information” includes the “pump number (70c) whose level information is“ high ”and the“ drug name (A, B) ”of the“ library 24a with alert occurrence level information ”in FIG. , C) "," drug information "," color information ", and further," information for alerting ".

That is, the “drug library information 44a with the third alert information” includes the drug name, the drug information, the color information, and the alert information that can be handled by the pump number (70c) whose alert occurrence frequency is “high”. The information is associated with “pump number (70c)”.

Next, the process proceeds to ST23. In ST23, the “communicable infusion pump information storage unit 33” and the “drug library information storage unit 44 with third alert information” in FIG. 5 are referred to.
In ST24, does the pump number (70a, 70b, 70c) of the “communicable infusion pump information storage unit 33” match the pump number (70c) of the “drug library information storage unit 44 with third alert information”? Judge whether or not.

When the pump numbers match in ST24, the process proceeds to ST25. In ST25, the drug name, the drug information, and the color information are associated with the alert information based on “the drug library information with the third alert information 44a” in the “third drug alert information with the alert information 44” of FIG. It is displayed on the infusion pump 70c and the like.

In other words, in the present embodiment, when the “third drug alert information-added drug library information 44a” is applicable, the infusion pump 70c is assumed to be an infusion pump with a high occurrence frequency of alerts. “Awareness” information is displayed in association with all drug names and the like displayed on the display 71 ”, and the nurse or the like is alerted.

On the other hand, when the pump number of the infusion pump 70 does not match in ST24, the process proceeds to ST26 in FIG. In ST26, the pump number (70a, 70b, 70c) of the “communicable infusion pump information storage unit 33” and the pump number (70c) of the “drug library information storage unit 44 with third alert information” do not match. It is determined that the infusion pump is not an infusion pump having a high alert frequency, and the “drug library information storage unit 42 with second alert information” in FIG. 6 is referred to.

Next, proceed to ST27. In ST27, whether or not “time zone information” associated with the “warning information” is specified in “drug library information with second alert information” in “second drug alert information storage section with second alert information” 42. Determine whether.

In the example of “drug library information with second alert information” in FIG. 6, for example, “drug library information with a second alert information 35a-a” is “6-12 o'clock” for drug B The information is associated with “warning information”.
Therefore, in the case of this example, it is assumed that “attention” information and “time zone information” are associated with each other, and the process proceeds to ST28.

In ST28, it is determined whether or not the current time corresponds to this “time zone information”, and “6-12 o'clock” in the above example.
If it is determined in ST28 that it corresponds, the process proceeds to ST29. In ST29, the drug name (A, B, C), drug information, and color information shown in “drug library information 35a-a with second alert information” in FIG. 6 are displayed, and drug name A and drug name B are displayed. Since the alert is frequently generated, “alert” information is associated and displayed on the “infusion pump-side display 71” such as the infusion pump 70a.

As described above, in the present embodiment, the alert information is not displayed in association with all drug names or the like, but a drug with a high occurrence frequency of an alert and / or a drug has a high occurrence frequency period. Select and display. The infusion pump is selected and displayed.
For this reason, the “Warning” information is not displayed for all drug names, etc., and is displayed by selecting the necessary cases. Therefore, effective “cautions” that do not make nurses and other users feel annoying the display. "Arouse" can be displayed.

On the other hand, in ST27, when “time zone information” associated with “warning information” is not specified in “medical drug library information with second alert information”, “with second alert information” in the example of FIG. In the case of the “drug library information 35a-b”, it is displayed on the “infusion pump side display 71” such as the infusion pump 70a as per the information (ST30).

That is, the medicine name (A, B, C), the medicine information, and the color information are displayed, and only the medicine A is displayed in association with the “warning” information.
In the case of “drug library information 35b-b with second alert information” in the example of “drug library information storage unit 42 with second alert information” in FIG. 6, the “notice” information is not displayed. An example.

As described above, in the present embodiment, the case where the frequency of occurrence of alerts is high is divided into cases according to the infusion pump, the drug name, the time zone, and the like, and is determined in detail. And when displaying these information on the infusion pump 70a etc., it is set as the structure which performs this display, only when "attention alert" is required, respectively.
Therefore, it is possible to accurately “warn” a medical staff such as a nurse who operates the infusion pump 70a and the like, and the nurse or the like is not bothered by an unnecessary display.

Further, in the present embodiment, as shown in FIGS. 7 and 8, etc., alert information generated during the operation of the infusion pump 70a, etc. is automatically acquired, and it is necessary to display “warning” based on these alert information. It is the structure which judges a new case and updates.
Therefore, even if the alert occurrence frequency is set to be high or low once and the “warning” information is displayed or hidden, it is automatically hidden or displayed depending on the subsequent alert occurrence frequency. The configuration is changed.
Thus, in this embodiment, since it is not necessary for a nurse or the like to access the drug library server or the like to change the display or non-display of the “warning” information, the drug library system 1 and the extremely easy to use It has become.

By the way, the present invention is not limited to the above-described embodiment. In the present embodiment, the infusion pump 70a and the like have been described as an example of the medical device, but the present invention is not limited to this, and can be suitably applied to other medical devices such as a syringe pump.

DESCRIPTION OF SYMBOLS 1 ... Drug library system, 10 ... Drug library server, 11 ... Server control part, 12 ... Server side input device, 13 ... Server side display, 14 ... Server side communication apparatus, DESCRIPTION OF SYMBOLS 20 ... 1st various information storage part, 21 ... Server side alert information storage part, 21a ... Server side alert information, 22 ... Alert generation level judgment part (program), 23 ... Alert generation High and low reference information storage unit, 24... Alert generating drug information storage unit with high and low information, 24 a... Alert generating chemical library with high and low information, 30... Second various storage units, 31. Height information storage unit, 31a... Alert generation level information for each pump, 32... Communicable pump identification unit (program), 33. Information storage unit, 34... First alert information display availability determination unit (program), 35... Drug library information storage unit with first alert information, 35 a, 35 b .. Drug with first alert information Library information, 35a-a, 35b-a, 35a-b, 35b-b ... Drug library information with second alert information, 40 ... Third various information storage unit, 41 ... Second alert Information display availability determination unit (program), 42 ... medicine library information storage unit with second alert information, 43 ... third alert information display availability determination unit (program), 44 ... third alert Drug library information storage unit with information, 44a ... Drug library information with third alert information, 70a, 70b, 70c ... Infusion pump, 71 ... Infusion pump side display, 72 ... Infusion pump side input device, 73 ... Infusion pump control unit, 74 ... Infusion pump side communication device, 75 ... Infusion pump body unit, 76 ... Alert signal generator, 77 ... Pump side alert Information storage unit, 77a ... Alert information on the pump side

Claims (5)

1. A medical information management device for providing drug information to a medical device,
   When providing the drug information, the alert information regarding the drug information can be provided in association with the drug information,
   The medical information management apparatus according to claim 1, wherein the provision of the alert information is configured to determine whether or not it is necessary based on occurrence frequency information of warning information that has actually occurred regarding the medicine.
2. The medical information management apparatus according to claim 1, wherein whether or not it is necessary to provide the alert information is determined based on occurrence frequency information of the warning information generated in the medical device. .
3. The occurrence frequency information of the warning information includes the time zone information of the occurrence, and the alert information is provided to the medical device when it corresponds to the time zone information with the high occurrence frequency of the warning information. The medical information management apparatus according to claim 1, wherein the medical information management apparatus is a medical information management apparatus.
4. The occurrence frequency information of the warning information is collected for each medical device, and the alert information is provided to the medical device having a high occurrence frequency. The medical information management apparatus according to any one of claims 3 to 3.
5. A medical information management method for providing drug information to a medical device,
   When providing the drug information, the alert information regarding the drug information can be provided in association with the drug information,
   The provision of the alert information is configured to determine whether or not the provision of the alert information is necessary based on the occurrence frequency information of the warning information that has actually occurred.

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