CN117954127B - Reasonable medication judgment method, medication rule data processing method and system - Google Patents
Reasonable medication judgment method, medication rule data processing method and system Download PDFInfo
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Abstract
The invention discloses a reasonable medication judgment method and a medication rule data processing method and system, and relates to the technical field of electronic information. The method comprises the steps that a first terminal logs in a prescription form issuing module of a service system, fills in prescription form information and sends out a medication verification request, a reasonable medication database reads medication characteristics in the prescription form information, invokes a custom medication rule with a user ID tag and a medication rule with a platform ID tag stored in the reasonable medication database according to a user ID and a user associated platform ID in the medication request information, traverses the medication rule, verifies the medication characteristics, and sends out a medication reasonable judgment notification to the first terminal if the medication characteristics are verified to have the consistent medication rule; otherwise, a notice of unreasonable medication judgment is sent to the first terminal. In the invention, a doctor can create a custom medication rule and store the custom medication rule in a reasonable medication database, so that the problem that the medication rule can only output unqualified conclusions when the application is out of range is avoided.
Description
Technical Field
The invention relates to the technical field of electronic information, in particular to a reasonable medication judgment method, a medication rule data processing method and a system.
Background
The concept of rational medication refers to the selection of the optimal drugs and their formulations according to the disease type, patient condition and pharmacological theory, and the formulation or adjustment of the dosage regimen in order to effectively, safely and economically prevent and cure the disease. Firstly, it is required to make accurate diagnosis of the disease, so that optimum medicine is selected according to the cause of disease and main symptoms, proper dosage is given through proper medication route, and proper treatment course is completed according to reasonable time interval, so as to achieve the expected treatment goal.
Along with the development of internet medical treatment, reasonable medication related technologies have also been developed. The reasonable medication judgment refers to that medication information is input into a medication rule, and the medication rule outputs whether medication is reasonable or not to assist in decision making.
Some main application scenarios of the existing reasonable medicine are: 1. the medical insurance system judges whether the medication is reasonable; 2. the prescribing doctor is used for assisting the self-decision to judge whether the medication is reasonable or not and helping the self-reminding self-prescribing problem.
According to the conventional reasonable medication judging method, a system developer develops a related reasonable medication system for authorized users to use, and a judgment result of whether the medication is reasonable or not is output to a corresponding user through inputting information into the reasonable medication system by a medication rule, so that the decision of the user is assisted. For example, chinese patent document cn202211428782.X discloses a system for checking and serving pharmacy rules based on a knowledge base, where an application scenario is to provide services for a medical insurance system, and a corresponding user is the medical insurance system. The reasonable medication system is developed by a system developer and provided for the medical insurance system to be called.
For example, chinese patent document CN202310497176.1 discloses a method, a system and an intelligent pharmacy for intelligent monitoring of big data prescription based on internet of things, which provides a medication monitoring module for a pharmacist in a medication scene, and a system developer develops the medication monitoring module.
Therefore, in the method in the prior art, the system developer is mainly relied on to provide the medication rule of reasonable medication, and the system developer is generally a worker related to the software development field, and is not well aware of medical knowledge, so that the created medication rule is created based on the medication rule constrained by the medicine specification, but in the practical application in the medical field, there are many medicine applications beyond the specification range, and the result output by adopting the medication rule is unreasonable.
The Chinese patent document CN201610799959.5 discloses a method for processing the medication information of the super instruction book, wherein a medication specification database of the super instruction book is established to supplement a reasonable medication database of the instruction book, and in the technology, an auditing step is required to be introduced in an auditing process to carry out auditing on the rule of the super instruction book medication, and the real-time supplement and update of the medication database cannot be realized reasonably so as to meet the requirements of first-line doctors.
Disclosure of Invention
The invention aims to provide a reasonable medication judgment method, a medication rule data processing method and a system, which can create a custom medication rule only for self use, wherein the custom medication rule can also be pushed to a platform and popularized and used by the platform.
In order to achieve the above object, the present invention adopts the following technical scheme:
the reasonable medication judgment method comprises the following steps:
the method comprises the steps that a first terminal logs in a prescription form issuing module of a service system, fills in prescription form information and sends out a medication verification request, a reasonable medication database reads medication characteristics in the prescription form information, invokes a custom medication rule with a user ID tag and a medication rule with a platform ID tag stored in the reasonable medication database according to a user ID and a user associated platform ID in the medication request information, traverses the medication rule, verifies the medication characteristics, and sends out a medication reasonable judgment notification to the first terminal if the medication characteristics are verified to have the consistent medication rule; otherwise, sending out a notice of unreasonable medication judgment to the first terminal;
The prescription information comprises a user ID, a user association platform ID, patient basic information, patient disease information and patient medication information; the basic information of the patient comprises the name, age, sex, past medical history and allergy history of the patient; the disease information is disease name, and the disease medication information comprises medicine name, medication period, medication frequency and medication amount;
The medication characteristics comprise patient basic information, patient disease information and patient medication information;
The medication rule comprises a drug name and a rule formula associated with the drug name; the rule formula constrains the application range and application method of the medicine; the application range refers to the disease, sex, age, past medical history and allergic history; the medication method refers to the aimed medication period, medication frequency and medication quantity;
The first terminal is a user side used by an associated doctor under the medical platform;
the implementation method of the drug administration rule with the platform ID tag comprises the following steps:
the second terminal logs in the service system, acquires user rights and configures platform information, configures medication rules used by the platform from a reasonable medication database, extracts configurator features from reasonable medication data, and marks the configured medication rules with platform ID tags; the second terminal is a management end used by a medical platform manager;
the implementation method for the drug administration rule with the user ID tag comprises the following steps:
The doctor user logs in a rule editing module of the service system through the first terminal, configures a self-defined medication rule, marks a user ID tag by the self-defined medication rule and stores the user ID tag in a reasonable medication database.
The medication rule data processing method comprises the following steps:
Storing medication rules with different labels in a reasonable medication database, wherein the implementation comprises the following steps:
the general drug administration rules created by the developer are stored in a reasonable drug administration database, the characteristics of the creator are extracted from the reasonable drug administration database, and the general label is marked on the drug administration rules;
The platform configures a medication rule set from a reasonable medication database through the second terminal, wherein the medication rule set comprises a plurality of medication rules which are common to platform-associated users, the reasonable medication database extracts configurator characteristics, and the configured medication rules are marked with platform ID labels;
The user self-defines the medication rule through the first terminal and stores the medication rule into a reasonable medication database, the reasonable medication database extracts creator characteristics, and the user ID tag is marked on the self-defined medication rule;
Further, the implementation method for storing the medication rules with the universal label and the platform ID label in the reasonable medication database comprises the following steps:
Step A1: the second terminal logs in a service system, acquires user rights and configures platform information; the platform information includes a platform ID;
step A2: the second terminal logs in a rule configuration interface of the service system, and the rule configuration interface maps the medication rules with universal labels in the reasonable medication database; the second platform configuration platform adopts a medication rule set, a reasonable medication database extracts configurator characteristics, and all medication rules with universal labels in the medication rule set are marked with platform ID labels;
Further, the implementation method for storing the medication rules with the platform ID tag and the user ID tag in the reasonable medication database comprises the following steps:
step B1: the method comprises the steps that a first terminal logs in a service system, obtains user rights and configures user information; the user information comprises a user ID, a user association platform ID and a medical department to which the user belongs.
Step B2: the method comprises the steps that a rule editing module of a first terminal logging in a business system creates a self-defined medication rule and stores the self-defined medication rule into a reasonable medication database, the reasonable medication database extracts creator characteristics, and a user ID label is marked on the self-defined medication rule;
Step B3: the method comprises the steps of calling a medication rule with a general label and a custom medication rule with a user ID label in a reasonable medication database, and mapping and pushing the medication rule to a rule configuration module of a second terminal corresponding to a user association platform;
Step B4: the second terminal logs in a rule configuration module of the service system, a configuration platform adopts a medication rule set, the configured medication rule set comprises a user-defined medication rule, a reasonable medication database extracts characteristics of a configurator, and the user-defined medication rule is marked with an ID label of the platform.
As a preferable technical scheme, a medicine rule with a general label is obtained by a developer through a crawler mode, and the general medicine rule is created by extracting data according to a set medicine rule format.
In the step B3, a reasonable medication database reads the custom medication rules, records the storage quantity of the same custom medication rules with different user ID tags in the reasonable medication database, calculates the autonomous creation rate P of the custom medication rules, and pushes the custom medication rule mapping to a rule configuration module pushed to all the second terminals when the autonomous creation rate P of the custom medication rules reaches a threshold.
As a preferred technical solution, the autonomous creation rate p=the storage number N of the same custom medication rules of different user ID tags/the number T of users of the medical department to which the custom medication rules belong;
The method for acquiring the number T of users in the medical department to which the self-defined medication rule belongs comprises the following steps:
extracting keywords of disease names in the self-defined medication rules, and matching medical departments according to the keywords; medical department information is stored in the reasonable medication database, and comprises medical department descriptions and medical department indications, medical department indications and medical department indications labels, wherein the medical department descriptions and the medical department indications are related to medical departments;
and according to the medical department, invoking user information stored in a reasonable medication database to obtain the registered user quantity T of the medical department.
The medication rule data processing system comprises a business system and a reasonable medication database; the business system interacts with the reasonable medication database information; the business system comprises a user management module, a platform management module, a prescription issuing module, a rule configuration module and a rule editing module;
the user management module is used for enabling a user to configure user information and store the user information into the reasonable medication database, authenticating and logging in and verifying a user account, verifying credentials provided by the user and authorizing the user to access;
The platform management module is used for configuring platform information, managing the authority and roles of the user account, distributing and controlling the access authority of the user to different resources and functions of the system, and adjusting and updating the authority according to the requirement;
The prescription form issuing module is used for filling prescription form information and sending a verification request to the reasonable medication database by a user;
the rule configuration module displays a rule configuration interface, maps the medication rules in the reasonable medication database, and configures the medication rules adopted by the platform through the login of the second terminal by the platform manager, so as to configure the medication rule set adopted by the platform;
The rule editing module is used for providing a rule editing guide bar and guiding a user to edit the medication rule according to a specified format;
The reasonable medication database stores medication rules, platform information, user information and medical department information; the reasonable medication database receives the verification request, extracts medication characteristics in prescription information and invokes medication rules to verify the medication characteristics; the reasonable medication database reads the characteristics of the creator and the characteristics of the configurator of the medication rules and marks the medication rules with labels; the reasonable medication database counts the same self-defined medication rule data and counts the number of registered users of the medical department to which the self-defined medication rule belongs, and the autonomous creation rate of the self-defined medication rule is calculated based on the data. .
Compared with the prior art, the invention has the following beneficial effects:
The doctor can create the custom medication rules and store the custom medication rules into the database, and when the prescription medication inspection is performed, the reasonable medication database can verify the custom medication rules of the doctor and the general medication rules of the platform, so that the problem that the medication rules can only output unqualified conclusions when the application is out of range is avoided.
The doctor can configure the customized rule through the first terminal, the same medication rule data customized by different doctors are counted, the autonomous creation rate is calculated, and the second terminal can be pushed by a developer according to the fact that the autonomous creation rate is equivalent to the examination of multiple doctors completing the customized medication rule, so that the same customized rule is configured to a certain proportion. On the basis, a doctor can establish a self-defined risk rule in real time for self-checking, the established self-defined risk rule is also stored in a reasonable medication database and is supplemented to the proper medication database in real time, when the same self-defined risk rule under different user ID labels reaches a threshold value, the self-defined risk rule can be popularized and used, the self-defined risk rule is updated and supplemented in real time, and the multi-doctor real-time examination is carried out in a mode of the self-defined risk rule.
Drawings
FIG. 1 is a flow chart of a rational medication judgment method in the present invention;
FIG. 2 is a flow chart of the user-defined medication rule with both user ID tag and platform ID tag according to the present invention.
Detailed Description
The technical solutions of the embodiments of the present invention will be clearly and completely described below in conjunction with the embodiments of the present invention, and it is apparent that the described embodiments are only some embodiments of the present invention, not all embodiments. All other embodiments, which can be made by those skilled in the art based on the embodiments of the invention without making any inventive effort, are intended to be within the scope of the invention.
Example 1
As shown in FIG. 1, a reasonable medication judgment method is realized by the following steps:
the method comprises the steps that a first terminal logs in a prescription form issuing module of a service system, fills in prescription form information and sends out a medication verification request, a reasonable medication database reads medication characteristics in the prescription form information, invokes a custom medication rule with a user ID tag and a medication rule with a platform ID tag stored in the reasonable medication database according to a user ID and a user associated platform ID in the medication request information, traverses the medication rule, verifies the medication characteristics, and sends out a medication reasonable judgment notification to the first terminal if the medication characteristics are verified to have the consistent medication rule; otherwise, sending out a notice of unreasonable medication judgment to the first terminal;
The prescription information comprises a user ID, a user association platform ID, patient basic information, patient disease information and patient medication information; the basic information of the patient comprises the name, age, sex, past medical history and allergy history of the patient; the disease information is disease name, and the disease medication information comprises medicine name, medication period, medication frequency and medication amount;
The medication characteristics comprise patient basic information, patient disease information and patient medication information;
The medication rule comprises a drug name and a rule formula associated with the drug name; the rule formula constrains the application range and application method of the medicine; the application range includes symptoms, gender, age, past medical history and allergy history; the administration method comprises administration period, administration frequency and administration amount;
the first terminal is a user side used by an associated doctor under the medical platform.
The medication rule data processing method is characterized by comprising the following steps:
marking a plurality of medication rules with different labels and storing in a rational medication database, the implementation comprising:
the general drug administration rules created by the developer are stored in a reasonable drug administration database, the characteristics of the creator are extracted from the reasonable drug administration database, and the general label is marked on the drug administration rules;
The platform configures a medication rule set from a reasonable medication database through the second terminal, wherein the medication rule set comprises a plurality of medication rules which are common to platform-associated users, the reasonable medication database extracts configurator characteristics, and the configured medication rules are marked with platform ID labels;
The user self-defines the medication rule through the first terminal and stores the medication rule into a reasonable medication database, the reasonable medication database extracts creator characteristics, and the user ID tag is marked on the self-defined medication rule;
the method for realizing the medication rule with the universal label and the platform ID label simultaneously stored in the reasonable medication database comprises the following steps:
Step A1: the second terminal logs in a service system, acquires user rights and configures platform information; the platform information includes a platform ID;
step A2: the second terminal logs in a rule configuration interface of the service system, and the rule configuration interface maps the medication rules with universal labels in the reasonable medication database; the second platform configuration platform adopts a medication rule set, a reasonable medication database extracts configurator characteristics, and all medication rules with universal labels in the medication rule set are marked with platform ID labels;
as shown in fig. 2, the implementation method for storing the medication rules with the platform ID tag and the user ID tag in the reasonable medication database includes the following steps:
Step B1: the method comprises the steps that a first terminal logs in a service system, obtains user rights and configures user information; the user information comprises a user ID, a user association platform ID and a medical department to which the user belongs;
Step B2: the method comprises the steps that a rule editing module of a first terminal logging in a business system creates a self-defined medication rule and stores the self-defined medication rule into a reasonable medication database, the reasonable medication database extracts creator characteristics, and a user ID label is marked on the self-defined medication rule;
Step B3: the method comprises the steps of calling a medication rule with a general label and a custom medication rule with a user ID label in a reasonable medication database, and mapping and pushing the medication rule to a rule configuration module of a second terminal corresponding to a user association platform;
Step B4: the second terminal logs in a rule configuration module of the service system, a configuration platform adopts a medication rule set, the configured medication rule set comprises a user-defined medication rule, a reasonable medication database extracts characteristics of a configurator, and the user-defined medication rule is marked with an ID label of the platform.
In some possible embodiments, the medication rules with the universal label are obtained by a developer through a crawler mode, and the data are extracted to create the universal medication rules according to the set medication rule format.
Custom medication rules are custom medication rules that are not created by the developer, but are used by the physician according to his own clinical experience, use experience, and medical trends.
Of course, the customized medication rule used by the doctor can be pushed to the associated platform management side, the management side can judge the rule and judge whether the rule is suitable for the platform, if so, the rule can be configured as the rule used by the platform, and therefore the customized medication rule of the doctor can be popularized to the whole platform.
Because a plurality of doctor users belonging to the platform exist under one platform, a scene that a plurality of users respectively establish a self-defined medication rule set under one platform can appear, and the self-defined medication rules established by different users have the same rule in the scene. And respectively creating custom medication rules at doctor users belonging to different platforms, wherein the created custom medication rules have the same custom medication rules.
The higher the autonomous creation rate of the same custom medication rules, the higher the actual application rate of the non-standard medication scheme. Based on this:
In some possible embodiments, in the step B3, the reasonable medication database reads the custom medication rules, records the storage number of the same custom medication rules with different user ID tags in the reasonable medication database, calculates the autonomous creation rate P of the custom medication rules, and when the autonomous creation rate P of the custom medication rules reaches a threshold, the reasonable medication database pushes the custom medication rule mapping to the rule configuration modules pushed to all the second terminals.
In some possible embodiments, the autonomous creation rate p=the stored number N of the same custom medication rules for different user ID tags/the number T of users of the medical department to which the custom medication rules pertain;
in some possible embodiments, the method for obtaining the number T of users in the medical department to which the custom medication rule belongs includes the following steps:
extracting keywords of disease names in the self-defined medication rules, and matching medical departments according to the keywords; medical department information is stored in the reasonable medication database, and comprises medical department information including medical department specifications and medical department indications associated with medical departments, and medical department indications and medical condition tags;
and according to the medical department, invoking user information stored in a reasonable medication database to obtain the registered user quantity T of the medical department.
Autonomous creation rate p=autonomous creation rate p=the stored number N of the same custom medication rules for different user ID tags/the number T of users of the medical department to which the custom medication rules pertain. Because the registered users of the whole system comprise various medical fields, the number of the registered users in different medical fields is different, and therefore, when the autonomous creation rate p of the medication rule is calculated, the number of the adopted users is the number of the registered users of the system of the medical department associated with the rule, so that the actual clinical application condition of the custom medication rule is more accurate.
Compared with the prior art, the self-defined medication rule data is a self-use standard which is automatically created by a user according to own working experience and clinical experience, and the self-use rule data is pushed to the second terminal according to the creation rate of the same self-use standard for the platform to perform reference configuration.
The whole self-defined reasonable medication database is updated in real time all the time in the actual work of doctors, the reasonable medication database provides medication rules for the doctors, and the doctors are continuously supplementing the reasonable medication database, so that the relevance between the whole medication rule database and the first-line actual clinical work is stronger, and the medication rules are updated in real time.
When the autonomous creation rate of the medication rule reaches a certain proportion, the actual use of the medication rule is shown to reach a certain degree, which is equivalent to that when doctors autonomously create the medication rule, the same medication rule is created, namely, equivalent to that different doctors mutually audit the medication rule, and the medication rule can be directly pushed to all platforms for configuration.
In the invention, whether the custom medication rule can be pushed to a platform or used by a full platform is judged, and the occurrence times of the same rule are automatically created by a doctor, so that whether the custom medication rule in a risk database can be configured for the full platform is judged, and whether the custom medication rule can be popularized to the full platform for configuration is judged without introducing a special team, so that the medication rule which can be pushed to the full platform for configuration in the reasonable medication database of the whole system can be automatically updated.
The medication rule is in the format of: a plurality of rules formulas associated with medication names;
the multiple regular formulas are constrained by logical operators and (sum).
The rule formula is: conditional label + conditional operator + conditional feature. Inputting a medicine name and a rule formula associated with the medicine name in a rule editing module, and providing a guide bar for editing the rule formula by the rule editing module;
Specifically, the condition labels include a base label and an optional label; the basic label is constraint information which is contained in each medication rule, and the optional label is constraint information which is optional in the medication rule;
The base label includes: sex, allergy history, diagnostic conditions, drug name, drug type, route of administration, upper limit of number of days of administration, upper limit of single dose, upper limit of frequency, lower limit of number of days of administration, lower limit of single dose, lower limit of frequency, age-limited minimum, age-limited maximum.
Optional labels include, but are not limited to: the upper limit of the number of administration days of the prescription box, the lower limit of the number of administration days of the prescription box, the prior medical history, whether pregnancy is present, liver function, kidney function.
The conditional operators include: = (equal to), ⊇ (inclusive), ++ ⊇ (exclusive), ∈ (belonging to), ∉ (not belonging to), > (greater than), < (less than), > = (greater than or equal to), <= (less than or equal to).
The condition features include: male, female, yes, no, external use, oral use, numbers referring to time, age, number, frequency, etc., and condition names, etc.
The associated medication rules of the same medicament are constrained by a logical operator or. The plurality of medication rules include general medication rules and custom medication rules.
The medication rule data processing system comprises a business system and a reasonable medication database; the business system interacts with the reasonable medication database information; the business system comprises a user management module, a platform management module, a prescription issuing module, a rule configuration module and a rule editing module;
the user management module is used for enabling a user to configure user information and store the user information into the reasonable medication database, authenticating and logging in and verifying a user account, verifying credentials provided by the user and authorizing the user to access;
The platform management module is used for configuring platform information, managing the authority and roles of the user account, distributing and controlling the access authority of the user to different resources and functions of the system, and adjusting and updating the authority according to the requirement;
The prescription form issuing module is used for filling prescription form information and sending a verification request to the reasonable medication database by a user;
the rule configuration module displays a rule configuration interface, maps the medication rules in the reasonable medication database, and configures the medication rules adopted by the platform through the login of the second terminal by the platform manager, so as to configure the medication rule set adopted by the platform;
The rule editing module is used for providing a rule editing guide bar and guiding a user to edit the medication rule according to a specified format;
The reasonable medication database stores medication rules, platform information, user information and medical department information; the reasonable medication database receives the verification request, extracts medication characteristics in prescription information and invokes medication rules to verify the medication characteristics; the reasonable medication database reads the characteristics of the creator and the characteristics of the configurator of the medication rules and marks the medication rules with labels; the reasonable medication database counts the same self-defined medication rule data and counts the number of registered users of the medical department to which the self-defined medication rule belongs, and the autonomous creation rate of the self-defined medication rule is calculated based on the data.
Thus, various embodiments of the present disclosure have been described in detail. In order to avoid obscuring the concepts of the present disclosure, some details known in the art are not described. How to implement the solutions disclosed herein will be fully apparent to those skilled in the art from the above description. It will be understood by those skilled in the art that the foregoing embodiments may be modified and equivalents substituted for elements thereof without departing from the scope and spirit of the disclosure. The scope of the present disclosure is defined by the appended claims.
Claims (1)
1. A reasonable medicine use judging method is characterized by comprising the following steps:
the method comprises the steps that a first terminal logs in a prescription form issuing module of a service system, fills in prescription form information and sends out a medication verification request, a reasonable medication database reads medication characteristics in the prescription form information, invokes a custom medication rule with a user ID tag and a medication rule with a platform ID tag stored in the reasonable medication database according to a user ID and a user associated platform ID in the medication request information, traverses the medication rule, verifies the medication characteristics, and sends out a medication reasonable judgment notification to the first terminal if the medication characteristics are verified to have the consistent medication rule; otherwise, sending out a notice of unreasonable medication judgment to the first terminal;
The prescription information comprises a user ID, a user association platform ID, patient basic information, patient disease information and patient medication information; the basic information of the patient comprises the name, age, sex, past medical history and allergy history of the patient; the disease information is disease name, and the disease medication information comprises medicine name, medication period, medication frequency and medication amount;
The medication characteristics comprise patient basic information, patient disease information and patient medication information;
The medication rule comprises a drug name and a rule formula associated with the drug name; the rule formula constrains the application range and application method of the medicine; the application range includes symptoms, gender, age, past medical history and allergy history; the administration method comprises administration period, administration frequency and administration amount;
The first terminal is a user side used by an associated doctor under the medical platform;
the data processing method of the medication rule comprises the following steps:
marking a plurality of medication rules with different labels and storing in a rational medication database, the implementation comprising:
the general drug administration rules created by the developer are stored in a reasonable drug administration database, the characteristics of the creator are extracted from the reasonable drug administration database, and the general label is marked on the drug administration rules;
The platform configures a medication rule set from a reasonable medication database through the second terminal, wherein the medication rule set comprises a plurality of medication rules which are common to platform-associated users, the reasonable medication database extracts configurator characteristics, and the configured medication rules are marked with platform ID labels;
the second terminal is a management end used by a medical platform manager;
The user self-defines the medication rule through the first terminal and stores the medication rule into a reasonable medication database, the reasonable medication database extracts creator characteristics, and the user ID tag is marked on the self-defined medication rule;
the method for realizing the medication rule with the universal label and the platform ID label simultaneously stored in the reasonable medication database comprises the following steps:
Step A1: the second terminal logs in a service system, acquires user rights and configures platform information; the platform information includes a platform ID;
step A2: the second terminal logs in a rule configuration interface of the service system, and the rule configuration interface maps the medication rules with universal labels in the reasonable medication database; the second platform configuration platform adopts a medication rule set, a reasonable medication database extracts configurator characteristics, and all medication rules with universal labels in the medication rule set are marked with platform ID labels;
the implementation method for storing the medication rules with the platform ID tag and the user ID tag in the reasonable medication database comprises the following steps:
Step B1: the method comprises the steps that a first terminal logs in a service system, obtains user rights and configures user information; the user information comprises a user ID, a user association platform ID and a medical department to which the user belongs;
Step B2: the method comprises the steps that a rule editing module of a first terminal logging in a business system creates a self-defined medication rule and stores the self-defined medication rule into a reasonable medication database, the reasonable medication database extracts creator characteristics, and a user ID label is marked on the self-defined medication rule;
Step B3: the method comprises the steps of calling a medication rule with a general label and a custom medication rule with a user ID label in a reasonable medication database, and mapping and pushing the medication rule to a rule configuration module of a second terminal corresponding to a user association platform;
step B4: the second terminal logs in a rule configuration module of the service system, a configuration platform adopts a medication rule set, the configured medication rule set comprises a user-defined medication rule, a reasonable medication database extracts the characteristics of a configurator, and the user-defined medication rule is marked with an ID label of the platform;
The medicine rule with the universal label is obtained by a developer through a crawler mode, and the general medicine rule is created by extracting the data according to a set medicine rule format;
In the step B3, the reasonable medication database reads the custom medication rules, records the storage quantity of the same custom medication rules with different user ID tags in the reasonable medication database, calculates the autonomous creation rate P of the custom medication rules, and pushes the custom medication rule mapping to the rule configuration module pushed to all the second terminals when the autonomous creation rate P of the custom medication rules reaches a threshold;
the autonomous creation rate p=the storage number N of the same custom medication rules of different user ID tags/the number T of users of the medical department to which the custom medication rules belong;
The method for acquiring the number T of users in the medical department to which the self-defined medication rule belongs comprises the following steps:
extracting keywords of disease names in the self-defined medication rules, and matching medical departments according to the keywords; medical department information is stored in the reasonable medication database, and comprises medical department descriptions and medical department indications, medical department indications and medical department indications labels, wherein the medical department descriptions and the medical department indications are related to medical departments;
and according to the medical department, invoking user information stored in a reasonable medication database to obtain the registered user quantity T of the medical department.
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