CN116421817A - Infusion pump control method, infusion apparatus, and storage medium - Google Patents

Infusion pump control method, infusion apparatus, and storage medium Download PDF

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Publication number
CN116421817A
CN116421817A CN202310336389.6A CN202310336389A CN116421817A CN 116421817 A CN116421817 A CN 116421817A CN 202310336389 A CN202310336389 A CN 202310336389A CN 116421817 A CN116421817 A CN 116421817A
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China
Prior art keywords
information
user
infusion pump
authority
display
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CN202310336389.6A
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Chinese (zh)
Inventor
李萍
唐亚洲
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Medcaptain Medical Technology Co Ltd
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Medcaptain Medical Technology Co Ltd
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Priority to CN202310336389.6A priority Critical patent/CN116421817A/en
Publication of CN116421817A publication Critical patent/CN116421817A/en
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    • G—PHYSICS
    • G06—COMPUTING; CALCULATING OR COUNTING
    • G06F—ELECTRIC DIGITAL DATA PROCESSING
    • G06F21/00—Security arrangements for protecting computers, components thereof, programs or data against unauthorised activity
    • G06F21/30—Authentication, i.e. establishing the identity or authorisation of security principals
    • G06F21/31—User authentication
    • G06F21/32—User authentication using biometric data, e.g. fingerprints, iris scans or voiceprints
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M5/00—Devices for bringing media into the body in a subcutaneous, intra-vascular or intramuscular way; Accessories therefor, e.g. filling or cleaning devices, arm-rests
    • A61M5/14—Infusion devices, e.g. infusing by gravity; Blood infusion; Accessories therefor
    • A61M5/142—Pressure infusion, e.g. using pumps
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M5/00—Devices for bringing media into the body in a subcutaneous, intra-vascular or intramuscular way; Accessories therefor, e.g. filling or cleaning devices, arm-rests
    • A61M5/14—Infusion devices, e.g. infusing by gravity; Blood infusion; Accessories therefor
    • A61M5/168—Means for controlling media flow to the body or for metering media to the body, e.g. drip meters, counters ; Monitoring media flow to the body
    • A61M5/16831—Monitoring, detecting, signalling or eliminating infusion flow anomalies
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M5/00—Devices for bringing media into the body in a subcutaneous, intra-vascular or intramuscular way; Accessories therefor, e.g. filling or cleaning devices, arm-rests
    • A61M5/14—Infusion devices, e.g. infusing by gravity; Blood infusion; Accessories therefor
    • A61M5/168—Means for controlling media flow to the body or for metering media to the body, e.g. drip meters, counters ; Monitoring media flow to the body
    • A61M5/16886—Means for controlling media flow to the body or for metering media to the body, e.g. drip meters, counters ; Monitoring media flow to the body for measuring fluid flow rate, i.e. flowmeters
    • A61M5/1689—Drip counters
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M5/00—Devices for bringing media into the body in a subcutaneous, intra-vascular or intramuscular way; Accessories therefor, e.g. filling or cleaning devices, arm-rests
    • A61M5/36—Devices for bringing media into the body in a subcutaneous, intra-vascular or intramuscular way; Accessories therefor, e.g. filling or cleaning devices, arm-rests with means for eliminating or preventing injection or infusion of air into body
    • A61M5/365—Air detectors
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M2205/00—General characteristics of the apparatus
    • A61M2205/18—General characteristics of the apparatus with alarm
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M2205/00—General characteristics of the apparatus
    • A61M2205/33—Controlling, regulating or measuring
    • A61M2205/3331—Pressure; Flow
    • A61M2205/3334—Measuring or controlling the flow rate
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M2205/00—General characteristics of the apparatus
    • A61M2205/50—General characteristics of the apparatus with microprocessors or computers
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P90/00—Enabling technologies with a potential contribution to greenhouse gas [GHG] emissions mitigation
    • Y02P90/02—Total factory control, e.g. smart factories, flexible manufacturing systems [FMS] or integrated manufacturing systems [IMS]

Abstract

The application provides an infusion pump control method, an infusion device and a storage medium. The method comprises the following steps: acquiring first user information through an authentication information acquisition module; acquiring stored user authority information; and determining display information output by the display module according to the acquired first user information and user authority information. In the method, the display information output by the display module corresponds to the current user, so that the current user can only check the display information within the authority range of the current user, the user is prevented from checking the infusion pump at will, and the safety of the infusion process is improved.

Description

Infusion pump control method, infusion apparatus, and storage medium
Technical Field
The present application relates to the field of medical technology, and in particular, to an infusion pump control method, an infusion apparatus, and a storage medium.
Background
In the process of infusion of a patient, the infusion conditions such as the infusion state of the patient, the infusion parameters of the medicine and the like can closely influence the treatment effect of the patient, seriously damage even life, so that the operation of the infusion pump in the process of infusion can not be controlled by professionals, and other people can not operate at will.
However, in the prior art, an unrelated user can randomly check related information of the infusion pump, so that the possibility of stopping infusion or modifying a treatment scheme exists in the process of infusing the patient, and the safety of the patient in the process of infusing is low.
Disclosure of Invention
The application provides an infusion pump control method, infusion equipment and a storage medium, which are used for solving the problem that in the prior art, an irrelevant user checks related information of an infusion pump at will, so that the safety in the infusion process is lower.
In a first aspect, the present application provides a method for controlling an infusion pump, applied to an infusion pump, the infusion pump including: the infusion pump control method comprises the following steps of:
acquiring first user information through an authentication information acquisition module;
acquiring stored user authority information;
and determining display information output by the display module according to the acquired first user information and user authority information.
In a second aspect, the present application provides a method for controlling an infusion pump, applied to the infusion pump, the infusion pump comprising: the infusion pump control method comprises the following steps of:
Acquiring first user information through the authentication information acquisition module;
acquiring stored user authority information;
receiving an operation request of the user through the input module;
and judging that the operation request does not meet the operation authority according to the acquired first user information and user authority information, and outputting prompt information and/or not executing operation processing corresponding to the operation instruction through the output module.
In a third aspect, the present application provides an infusion device comprising: a processor, a memory having code stored therein, the processor executing the code stored in the memory to perform the infusion pump control method of any one of the first or second aspects.
In a fourth aspect, the present application provides a computer readable storage medium having stored therein computer executable instructions which when executed by a processor are adapted to carry out the infusion pump control method of any of the first or second aspects.
In a fifth aspect, the present application provides a computer program product comprising a computer program which, when executed by a processor, implements the infusion pump control method of any one of the first or second aspects.
The application provides an infusion pump control method, an infusion device and a storage medium, wherein the method comprises the following steps: and acquiring first user information through an authentication information acquisition module, and acquiring stored user authority information. And determining display information output by the display module according to the acquired first user information and user authority information. The display information output by the display module corresponds to the current user, so that the current user can only check the information within the authority range of the current user, thereby effectively avoiding the check of the infusion pump by unrelated users and improving the safety of the infusion process.
Drawings
The accompanying drawings, which are incorporated in and constitute a part of this specification, illustrate embodiments consistent with the application and together with the description, serve to explain the principles of the application.
Fig. 1 is a schematic structural diagram of an infusion pump according to an embodiment of the present disclosure;
fig. 2 is a schematic view of a scenario of a user-operated infusion pump according to an embodiment of the present disclosure;
FIG. 3 is a flowchart illustrating a method for controlling an infusion pump according to an embodiment of the present disclosure;
fig. 4 is a flowchart two of an infusion pump control method according to an embodiment of the present disclosure;
fig. 5 is a schematic diagram of a triggering process of a secondary authentication operation instruction according to an embodiment of the present application;
Fig. 6 is a schematic diagram of a triggering process of a primary authentication operation instruction according to an embodiment of the present application;
fig. 7 is a flowchart III of a method for controlling an infusion pump according to an embodiment of the present disclosure;
FIG. 8 is a schematic diagram I of an infusion device according to an embodiment of the present disclosure;
fig. 9 is a schematic diagram II of an infusion device according to an embodiment of the present disclosure;
fig. 10 is a schematic diagram III of an infusion device according to an embodiment of the present disclosure.
Specific embodiments thereof have been shown by way of example in the drawings and will herein be described in more detail. These drawings and the written description are not intended to limit the scope of the inventive concepts in any way, but to illustrate the concepts of the present application to those skilled in the art by reference to specific embodiments.
Detailed Description
Reference will now be made in detail to exemplary embodiments, examples of which are illustrated in the accompanying drawings. When the following description refers to the accompanying drawings, the same numbers in different drawings refer to the same or similar elements, unless otherwise indicated. The implementations described in the following exemplary examples are not representative of all implementations consistent with the present application. Rather, they are merely examples of apparatus and methods consistent with some aspects of the present application as detailed in the accompanying claims.
It should be noted that, the user information (including but not limited to user equipment information, user personal information, etc.) and the data (including but not limited to data for analysis, stored data, presented data, etc.) related to the present application are information and data authorized by the user or fully authorized by each party, and the collection, use and processing of the related data need to comply with the related laws and regulations and standards of the related country and region, and provide corresponding operation entries for the user to select authorization or rejection.
The infusion pump is an intelligent infusion device and can accurately control the number of infusion drops or the infusion flow rate. The infusion pump is clinically applied, so that the accuracy and safety of infusion are improved. However, in the prior art, an unrelated user can check related information of the infusion pump at will and further operate according to the displayed information, so that the possibility of stopping infusion or modifying a treatment scheme exists in the process of infusing the patient, and the safety of the patient in the process of infusing is low.
To address this issue, a corresponding user right may be set for the relevant user using the infusion pump. The method comprises the steps of obtaining first user information of a current user and stored user authority information, and determining display information output by an infusion pump display module according to the first user information and the user authority information. Because the display information corresponds to the checking authority of the infusion pump owned by the current user, the current user can only check the information within the authority range of the current user and cannot check other display information outside the checking authority of the infusion pump, so that the user is prevented from operating the infusion pump at will, and the safety of the infusion process is effectively improved.
Fig. 1 is a schematic structural diagram of an infusion pump according to an embodiment of the present application, and as shown in fig. 1, the infusion pump may include a controller 10, an authentication information collecting module 20, an infusion executing module 30, an input module 40, an output module 50, and a detection module 60. The infusion execution module 30 may perform an infusion process, and may include a pump device 301, where the pump device 301 is configured to provide a power source for delivering fluid. The input module 40 may be used to set infusion parameters, etc. The output module 50 is configured to output infusion pump information and infusion parameters, and the like, and the output module 50 may include a display module 501 to display the infusion pump information and the infusion parameters via the display module 501. The detection module 60 may be formed of a plurality of sensors, such as an infrared drop number sensor that can detect the flow rate and flow rate of the liquid, an ultrasonic sensor that detects bubbles, and the like. The controller 10 is used for controlling the above-described plurality of modules.
The authentication information collection module 20 may include: a biological information acquisition module 201, a near field communication recognition module 202, an image recognition module 203, a voice recognition module 204, and the like. The biological information acquisition module 201 is configured to acquire biological information of an infusion pump operator, including fingerprint, iris, face information, etc., so the biological information acquisition module 201 may include at least one of the following: fingerprint collector, iris collector and face collector. The near field communication module 202 may be used to read information in the infusion pump operator NFC card. The image recognition module 203 may include a camera or the like for acquiring two-dimensional codes, bar codes, and other information such as authentication images. The voice recognition module 204 may include a voice capture device such as a microphone for obtaining voice information from an infusion pump operator. When a user uses the infusion pump, his user may also be authenticated by digital information, which may be entered via the input module 40 or the display module 501.
Fig. 2 is a schematic view of a scenario in which a user operates an infusion pump according to an embodiment of the present application, where, as shown in fig. 2, a fingerprint collection area of the infusion pump may collect fingerprint information of a current user, and unlock the infusion pump if verification is passed. After the unlocking is successful, the operation authority of the infusion pump corresponding to the user can be displayed on the display interface, and the user can select the operation authority to set the infusion pump.
The following describes the technical solution of the present application and how the technical solution of the present application solves the above technical problems in detail with specific embodiments. The following embodiments may be combined with each other, and the same or similar concepts or processes may not be described in detail in some embodiments. Embodiments of the present application will be described below with reference to the accompanying drawings.
Fig. 3 is a flowchart of an infusion pump control method according to an embodiment of the present application, where the infusion pump control method may be applied to an infusion pump. The infusion pump may comprise: a controller 10, an authentication information acquisition module 20, an infusion execution module 30, and a display module 501. The method of the present embodiment may be performed by an infusion device, may be the controller 10, and may be implemented in hardware, software, or a combination of hardware and software. As shown in fig. 3, the method may include:
S301: and acquiring the first user information through an authentication information acquisition module.
In some embodiments, the user is an operator of the infusion pump, and the first user information is related information for identifying and authenticating the user's identity, including but not limited to: fingerprint information, face information, iris information, digital information, image information, sound information, authentication information used by near field communication (Near Field Communication, NFC), and the like.
The authentication information acquisition module is used for acquiring first user information and comprises one or more of a biological information acquisition module, a near field communication recognition module, an image recognition module and a voice recognition module. Wherein the biological information acquisition module may acquire at least one of: fingerprint information, face information, and iris information. The near field communication module can collect first user information of a user based on NFC, bluetooth, wiFi and the like. The image recognition module may acquire two-dimensional code information, bar code information, other authentication images, and the like. The voice recognition module collects voice information of the user.
In some embodiments, when the first user information is digital information, the authentication information acquisition module may also be a touch screen or an entity key on the infusion pump, and the user may input the corresponding digital information by clicking the touch screen or pressing the entity key.
S302: and acquiring the stored user authority information.
In some embodiments, the user permission information is used to characterize permissions possessed by a user, including user identification information, infusion pump viewing permissions, and the like, wherein the user identification information corresponds one-to-one to the infusion pump viewing permissions. User identification information refers to information used to verify the identity of a user, such as a user name, password, fingerprint, etc. The infusion pump viewing authority defines that a user can view information of the infusion pump, such as the operating state of the device, the drug infusion rate, the drug dosage, etc. According to different user roles and operation requirements, different infusion pump viewing rights can be set for different users. For example, a doctor may have higher authority so that the drug infusion dose and rate may be altered, while a nurse may only need to view device status and records.
The user identification information is used to compare with the first user information and is of a type consistent with the type of the first user information, including but not limited to: fingerprint information, face information, iris information, digital information, image information, sound information, authentication information used by near field communication (Near Field Communication, NFC), and the like.
The infusion pump viewing authority is used to define information that a user can view through the infusion pump, and may include: information of the current infusion pump, infusion information, patient information, alarm information, etc. The information of the infusion pump may include: injection accuracy, injection mode, system state, display brightness, display contrast, etc. The infusion information includes infusion rate, type of drug infused, drug concentration, metering ratio, etc. Patient information may include information on the name, age, past chief complaints, recent diagnosis, recent treatment effect, etc. of the current patient. The alarm information is that the infusion pump can send out alarm information when the infusion abnormality occurs or the medicine dosage exceeds the set range, and the like, and the alarm information comprises alarm type, alarm sound and a corresponding processing method.
S303: and determining display information output by the display module according to the acquired first user information and user authority information.
In some embodiments, the infusion pump viewing authority corresponding to the first user information may be obtained from the user authority information based on the received first user information and user authority information. And outputting display information corresponding to the checking authority of the infusion pump on the display module.
In an alternative implementation, since the user permission information includes user identification information and infusion pump viewing permissions, the first user information may be verified based on the user identification information. If the verification is passed, the corresponding checking authority of the infusion pump is determined according to the user identification information, so that the checking authority of the infusion pump corresponds to the current first user information. After determining the checking authority of the infusion pump, the screen of the infusion pump can be unlocked, and corresponding display information is output on the display module.
In another alternative implementation, the user rights information may also include a user category. Because the users in the same user category can set the same user authority information, the mapping relation between the user identification information and the user category and the mapping relation between the user category and the user authority information can be preset. At the moment, the first user information of the user can be verified based on the user identification information, if the verification is passed, the user category corresponding to the current user identification information is determined, and then the user authority information corresponding to the user category is determined, so that the checking authority of the infusion pump corresponding to the first user information can be obtained.
The user categories may include a plurality of categories of doctors, nurses, patients, and the like. Here, the categories of doctors, nurses, and the like may be further refined. For example, doctors are refined into categories of surgeons, physicians, etc. according to the areas in which the doctors are located. The doctor can be thinned into a plurality of categories such as inpatients, mainly treating doctors and the like according to the role of the doctor. When the user permission information contains the user category, the user permission information of a plurality of users in the same user category can be adaptively modified by modifying the user permission information corresponding to the user category, so that the efficiency of modifying the user permission information of the plurality of users is improved.
In one or more embodiments of the present application, after the display module outputs the display information, the user may further operate and control the infusion pump based on the current display information. The user authority information may further include infusion pump operation authority information, and the infusion pump control method further includes: and judging that the operation instruction input by the user does not meet the corresponding operation authority according to the received first user information and the user authority information, and outputting prompt information and/or not executing the operation item corresponding to the operation instruction. Specifically, the prompt information can be output in the modes of characters, images, alarm sounds, indicator lights and the like. When the received first user information and user authority information judge that the operation instruction input by the user meets the corresponding operation authority, the infusion pump executes corresponding operation matters according to the corresponding operation instruction.
The infusion pump operation authority information is used for representing the authority of the current user for operating the infusion pump, and comprises at least one of the following: checking infusion information, drug selection, setting infusion parameters, infusion control, changing syringes or infusion bags, system settings, etc.
In another implementation scenario, if the verification of the first user information according to the user identification information fails, a prompt message may be output through the display module at this time, indicating that the current user does not have the authority to view the infusion pump.
The embodiment of the application provides an infusion pump control method, which comprises the steps of acquiring first user information through an authentication information acquisition module and acquiring stored user authority information. And determining display information output by the display module according to the acquired first user information and user authority information. The display information corresponds to the current user, so that the current user can only check the related information of the infusion pump according to the current display information, the use safety of the infusion pump is improved, and the safety in the infusion process is further improved.
In one or more embodiments of the present application, optionally, outputting, on the display module, display information corresponding to the infusion pump viewing authority may include:
determining corresponding display content and display modes according to the checking authority of the infusion pump;
determining display information by combining display contents and display modes;
and outputting display information on the display module.
For example, the display content may include one or more of information of the current infusion pump, infusion information, patient information, alarm information, user information of a user currently operating the infusion pump, and the like.
Wherein the information of the infusion pump is related information of the infusion pump device, and may include: one or more of injection accuracy, injection mode, system status, display brightness, display contrast, etc. The infusion information is information of the current infusion process and can comprise one or more of infusion rate, type of drug infused, drug concentration, metering ratio and the like. The patient information may include one or more of the name, age, past chief complaints, recent diagnostic conditions, recent therapeutic effects, etc. of the current patient. User information for a user currently operating an infusion pump may include name, job number, category, department, etc. The alarm information is the prompt information sent by the infusion pump when infusion abnormality occurs or the medicine dosage exceeds a set range, and can comprise one or more of alarm types, alarm sounds and alarm prompt information.
By way of example, the display may include one or more of a display color, a display brightness, a font format, a color and size, a page layout, etc. of the infusion pump display page. For example, if the infusion pump corresponding to the user has more display content of the viewing authority, the display content may be displayed in a tiled or paged manner. Different font formats, colors and sizes may also be determined according to different types of display content. For example, the information of the infusion pump is black, the information of the infusion pump is red, the information of the patient is green, and the like, which can be set according to different viewing authorities.
In summary, according to the current user's infusion pump viewing authority, the corresponding display content and display mode are determined. And determining display information by combining the display content and the display mode, and displaying on a display module. The displayed display information corresponds to the checking authority of the infusion pump which is possessed by the current user, and the display content does not contain the information corresponding to the checking authority which is not possessed by the current user, so that the current user can check the infusion pump only according to the display content, the situation that the user checks the related information of the infusion pump at will is effectively avoided, and the use safety of the infusion pump is effectively improved. Meanwhile, the display mode is determined according to the checking authority of the infusion pump of the current user, so that a better display effect is achieved, and the user experience is improved.
On the basis of the above embodiments, a specific embodiment will be provided below, describing a process of operating an infusion pump by a user.
Fig. 4 is a flowchart two of an infusion pump control method according to an embodiment of the present application, as shown in fig. 4, and the method specifically includes:
s401: and receiving an operation instruction input by a user.
The operation instruction is an instruction for performing operation control on the infusion pump, corresponds to the operation authority information of the infusion pump, and can comprise one or more of the following: checking infusion information, drug selection, setting infusion parameters, infusion control, changing syringes or infusion bags, system settings, etc.
Wherein the drug is selected as the type of drug that can be used and set by the current infusion pump operator. Setting infusion parameters is configuring the infusion pump and includes one or more of drug name, drug concentration, metering ratio, infusion rate, etc. The infusion information may be part or all of the infusion parameters. Infusion control may be one or more of controlling the start, stop, bolus, selection of infusion mode, modification of infusion parameters, etc. of the infusion process. Changing the syringe or infusion bag may be accomplished by controlling the infusion pump to place the switch of the pump door of the infusion tube. The system setting is to set one or more of a system state, a display brightness, a display contrast, a display mode, and the like.
In an implementation scenario, the user inputs the operation instruction, which may be implemented by pressing an entity key corresponding to the operation instruction, or may be implemented by clicking the corresponding operation instruction on a touch screen of the display module, and specifically, may be in multiple modes such as clicking, double clicking, long pressing, etc., which is not limited in this application.
S402: and confirming the authentication mode of the received operation instruction according to the received first user information and the received user authority information.
The user rights information includes user identification information and infusion pump operating rights.
The authentication mode corresponds to the authentication information acquisition module and comprises at least one of the following: biometric authentication, near field communication authentication, image information authentication, voice information authentication, digital information authentication, and the like. The biometric information authentication includes fingerprint information authentication, face information authentication, iris information authentication, and the like.
In some embodiments, different operation instructions may be set to different authentication modes. For example, the operation instruction of "checking infusion information" is fingerprint information authentication, the operation instruction of "drug selection" is image information authentication, the operation instruction of "setting infusion parameters" is near field communication authentication, and the like.
In an optional implementation manner, the user authority information further includes operation authority authentication information, and the operation authority authentication information includes authentication levels and/or authentication modes corresponding to different operation instructions. When the first user information is verified based on the user identification information, the operation authority authentication information corresponding to the first user information can be determined.
In some embodiments, different authentication levels may be set for different operation instructions depending on their importance, due to the different importance of the operation instructions. For example, the operation instruction may be set to at least two authentication levels, primary authentication and secondary authentication, respectively. The primary authentication is to perform one-time authentication on the current user, and the secondary authentication is to perform two-time authentication on the current user, or to perform two-time authentication on the upper level of the user. The operation command may be set to three or more authentication levels according to actual use requirements, and the number of authentication levels is not limited.
The operation instruction corresponding to the primary authentication or the operation instruction corresponding to the secondary authentication may include: one or more of infusion information, drug selection, setting infusion parameters, infusion control, changing syringes or infusion bags, system settings, etc. The operation instruction corresponding to the primary authentication and the operation instruction corresponding to the secondary authentication can be added, deleted or modified according to actual requirements.
S403: and outputting prompt information and/or executing no operation item corresponding to the operation instruction if the authority authentication fails according to the determined authentication mode.
Specifically, the output of the prompt information may be achieved in various manners, for example, error information is displayed on a display module of the infusion pump, flashing through an indicator light, and an audio prompt, and in which manner, the output may be selected according to the characteristics of the infusion pump and the requirements of the user. The infusion pump also prevents the user from performing the corresponding operating event while outputting the prompt message to avoid potential risks. For example, if the user does not have sufficient authority to change the settings of the infusion pump, the infusion pump may refuse to execute the corresponding instructions and display the corresponding prompts on the display module. For example, if the user inadvertently enters the wrong password, the system may refuse to perform the corresponding operation and prompt the user to enter the correct password.
In some embodiments, for some critical operations, such as stopping drug infusion or changing drug dosage, etc., after determining the authentication mode, the display module may display the corresponding authentication information by displaying an unlock operation window. After the user inputs the authentication information, authority authentication can be performed on the authentication information so as to ensure the safety and effectiveness of the use of the infusion pump.
In some embodiments, for the operation instruction of the second-level authentication, the same authentication mode may be adopted for the two-level authentication, or different authentication modes may be adopted for the two-level authentication, that is, different authentication information acquisition modules are adopted for the two-level authentication to acquire corresponding authentication information, so as to authenticate the authentication information and improve security. Fig. 5 is a schematic diagram of a triggering process of a secondary authentication operation instruction provided in the embodiment of the present application, and referring to fig. 5, taking an operation instruction triggered by a user as an example of "setting infusion parameters", after the user inputs the operation instruction of "setting infusion parameters", the operation instruction belongs to secondary authentication, and the first authentication mode is image information authentication, and the second authentication mode is voice information authentication. And after the two times of authentication are successful, controlling the display module to display a corresponding infusion parameter setting interface.
For the operation instruction of the second authentication, if there is a failure of one authority authentication in the two authentications, the prompt information is output and/or the operation item corresponding to the operation instruction is not executed. In one implementation scenario, if the first authentication fails in the two authentications, the prompt message may be directly output without performing the second authentication.
In another implementation scenario, if the authority authentication is successful according to the determined authentication mode, the infusion pump is controlled to execute the operation item corresponding to the operation instruction. For example, fig. 6 is a schematic diagram of a triggering process of a primary authentication operation instruction provided in the embodiment of the present application, and referring to fig. 6, if an operation instruction triggered by a user is "check infusion information", the operation instruction belongs to primary authentication, and the corresponding authentication mode is fingerprint information authentication. At this time, fingerprint information of the user can be acquired through the biological information acquisition module, and after the fingerprint information passes verification, the display module of the infusion pump is controlled to display current infusion information.
It should be noted that, the checking authority of the infusion pump and the operation authority of the infusion pump can be set with different authentication modes, so as to further authenticate the authority of the user and improve the safety of the infusion process. For example, the authentication mode of the infusion pump viewing authority may be bio-information authentication, i.e. the first user information is bio-information. The infusion pump operation authority may be one or more authentication modes other than the biometric authentication, such as image information authentication, voice information authentication, digital information authentication, near field communication authentication, and the like.
The embodiment of the application provides an infusion pump control method, which receives an operation instruction input by a user. And confirming the authentication mode of the received operation instruction according to the received first user information and the received user authority information. And outputting prompt information and/or executing no operation item corresponding to the operation instruction if the authority authentication fails according to the determined authentication mode. After the user inputs the operation instruction, the method of the embodiment of the application authenticates the operation instruction, avoids the operation of the infusion pump by the user without the operation authority of the infusion pump, and improves the safety. Meanwhile, the operation instructions are set to different authentication levels, and the operation instructions with higher importance are verified for multiple times, so that misoperation is avoided, and the safety in the operation process of the infusion pump is further improved.
It should be noted that, the user permission information related to the above embodiment may be adjusted before, during and after the infusion pump is used, and personalized user permission information may be set for different users. In one implementation scenario, the user permission information includes a user ID, and the user permission information corresponding to the current user may be adjusted according to the user ID.
In some embodiments, the user rights information may be adjusted by one or more of adding, deleting, modifying, or updating. For example, the user authority information includes user identification information, operation authority of the infusion pump, operation authority authentication information, and the like, wherein the operation authority authentication information further includes an authentication level and/or an authentication mode corresponding to the operation authority. Therefore, the user authority information is adjusted, and any information or a plurality of information can be modified. Specifically, the user identification information is updated, and/or the operation authority of the infusion pump is added or deleted, and/or the authentication level and/or the authentication mode of a certain operation authority are modified, etc.
On the basis of the above embodiments, an embodiment will be provided below, in which an infusion pump control method is described when a user operates an infusion pump.
Fig. 7 is a flowchart III of a control method of an infusion pump according to an embodiment of the present application, where the infusion pump includes: a controller 10, an authentication information acquisition module 20, an infusion execution module 30, an input module 40, and an output module 50. As shown in fig. 7, the method may include:
s701: and acquiring the first user information through an authentication information acquisition module.
The first user information is related information for identifying and authenticating the identity of the user, and comprises at least one of the following: biometric information, image information, voice information, digital information, authentication information used by near field communication, and the like. The biological information may include one or more of fingerprint information, face information, iris information, and the like.
The authentication information acquisition module is used for acquiring user information and comprises at least one of the following components: the device comprises a biological information acquisition module, a near field communication recognition module, an image recognition module and a voice recognition module. The biological information acquisition module can comprise one or more devices such as a fingerprint collector, a face collector, an iris collector and the like. The digital information can be input by a touch screen or physical keys.
S702: and acquiring the stored user authority information.
The user authority information comprises authority information owned by a plurality of users, including user identification information and infusion pump operation authority information. The infusion pump operation authority information comprises an infusion pump operation authority, an authentication level corresponding to the operation authority and/or an authentication mode.
In particular, the infusion pump operating rights information may include at least one of the following: checking infusion information, drug selection, setting infusion parameters, infusion control, changing syringes or infusion bags, system settings, etc.
Different infusion pump operating rights may set different authentication levels that characterize the number of times a user is authenticated. For example, a primary authentication means that a user needs to be authenticated once, a secondary authentication means that a user needs to be authenticated twice, a tertiary authentication means that a user needs to be authenticated three times, and so on. After the authentication is passed, the user can perform corresponding operation on the infusion pump.
The authentication mode corresponds to the authentication information acquisition module and indicates the mode of authentication of the operation authority of the infusion pump, and the authentication mode comprises at least one of the following steps: biometric authentication, near field communication authentication, image information authentication, voice information authentication, digital information authentication, and the like. Different authentication modes need to adopt different authentication information acquisition modules.
S703: and receiving an operation request of a user through an input module.
The input module may be a touch screen of the infusion pump or may be some physical key on the infusion pump. The user may send an operation request to the infusion pump by clicking a touch screen or pressing a corresponding physical key.
The operation request corresponds to infusion pump operation rights and may include one or more of the following: unlocking an infusion pump screen, checking infusion information, selecting medicines, setting infusion parameters, controlling infusion, replacing a syringe or an infusion bag, setting a system, and the like.
S704: and judging that the operation request does not meet the operation authority according to the acquired first user information and user authority information, and outputting prompt information and/or not executing operation processing corresponding to the operation instruction through an output module.
In some embodiments, upon receiving a user's operation request, the first user information may be verified based on the user identification information. After verification is passed, the operation authority information of the infusion pump corresponding to the first user information can be determined, and whether the operation request meets the operation authority information of the infusion pump of the current user can be further judged.
For example, the infusion pump operation authority information corresponding to the current user includes: check infusion information, infusion control, and replace syringes. If the operation request sent by the user to the infusion pump is "set infusion parameter", since the "set infusion parameter" is not within the operation authority information of the infusion pump of the current user, it may be determined that the operation request does not satisfy the operation authority. At this time, the output module may output the prompt information, and/or, the operation process corresponding to the operation instruction is not executed, that is, the interactive interface of "set infusion parameter" is not displayed.
In other embodiments, since different authentication levels and authentication modes exist in different operation authorities of the infusion pump, after the first user information is successfully verified based on the user identification information, the user needs to be verified again according to the authentication level and authentication mode corresponding to the operation request of the current user.
For example, if the operation request of "setting infusion parameters" is a secondary authentication, and the first authentication mode is near field communication authentication, the second authentication mode is digital information authentication. At this time, the first user information is successfully verified, and an unlocking operation window for near field communication authentication can be displayed, so that the user inputs corresponding authentication information based on near field communication. After the authentication is passed, an unlocking operation window for digital information authentication is displayed, and a user inputs corresponding digital information through an input module. After the re-authentication is passed, the infusion pump is controlled to display an interface of 'set infusion parameters'.
The output module can be a touch screen of the infusion pump, an alarm or an indicator light and other devices. Accordingly, the indication information is information for indicating that the user does not meet the operation authority, and includes but is not limited to text and/or image information displayed on a touch screen, sound information output by an alarm, state information of an indicator light and the like. For example, the indicator light may present a blinking state when the user's operation request does not satisfy the operation right.
The embodiment of the application provides an infusion pump control method, which comprises the steps of acquiring first user information through an authentication information acquisition module and acquiring stored user authority information. And receiving an operation request of a user through the input module, judging that the operation request does not meet the operation authority according to the first user information and the user authority information, and outputting corresponding prompt information through the output module and/or not executing operation processing corresponding to the operation instruction, so that the user without the operation authority cannot operate the infusion pump at will, and the safety of the infusion process is improved.
It should be noted that the execution body of the above method embodiment may be an infusion device. The infusion device may be integrated with the infusion pump or may be a separate device, such as a computer, where the computer may communicate with the infusion pump over a network to control the operational authority of the infusion pump.
Fig. 8 is a schematic diagram of an infusion device according to an embodiment of the present disclosure. As shown in fig. 8, an embodiment of the present application provides an infusion device 800 that may include an acquisition module 801 and a determination module 802.
An acquisition module 801, configured to acquire first user information through an authentication information acquisition module;
the acquiring module 801 is further configured to acquire stored user permission information;
the determining module 802 is configured to determine display information output by the display module according to the obtained user information and user permission information.
The apparatus of this embodiment may be used to execute the above-described method embodiments, and its implementation principle and technical effects are similar, and will not be described herein.
Fig. 9 is a schematic diagram of an infusion device according to an embodiment of the present disclosure. As shown in fig. 9, an infusion device 900 may include an acquisition module 901, a receiving module 902, a determining module 903, and an output module 904.
The acquisition module 901 is configured to acquire first user information through the authentication information acquisition module;
the acquisition module 901 is further configured to acquire stored user permission information;
a receiving module 902, configured to receive an operation request of a user through an input module;
the judging module 903 is configured to judge that the operation request does not satisfy the operation permission according to the acquired first user information and user permission information;
the output module 904 is configured to output the prompt information and/or not execute the operation processing corresponding to the operation instruction through the output module.
The apparatus of this embodiment may be used to execute the above-described method embodiments, and its implementation principle and technical effects are similar, and will not be described herein.
Fig. 10 is a schematic diagram III of an infusion device according to an embodiment of the present disclosure. As shown in fig. 10, an infusion device 1000 is provided in an embodiment of the present application, which includes a processor 1001 and a memory 1002, wherein the processor 1001 and the memory 1002 are connected by a bus 1003.
In a specific implementation, the memory 1002 stores code, and the processor 1001 executes the code stored in the memory 1002 to perform the infusion pump control method of the above-described method embodiment.
The specific implementation process of the processor 1001 may refer to the above method embodiment, and its implementation principle and technical effects are similar, and this embodiment will not be described herein again.
In the embodiment shown in fig. 10 described above, it should be understood that the processor 1001 may be a central processing unit (english: central Processing Unit, abbreviated as CPU), or may be other general purpose processors, digital signal processors (english: digital Signal Processor, abbreviated as DSP), application specific integrated circuits (english: application Specific Integrated Circuit, abbreviated as ASIC), or the like. A general purpose processor may be a microprocessor or the processor may be any conventional processor or the like. The steps of a method disclosed in connection with the present invention may be embodied directly in a hardware processor for execution, or in a combination of hardware and software modules in a processor for execution.
Memory 1002 may comprise high-speed RAM memory, and may also include non-volatile storage NVM, such as at least one magnetic disk memory.
The bus 1003 may be an industry standard architecture (Industry Standard Architecture, ISA) bus, an external device interconnect (Peripheral Component, PCI) bus, or an extended industry standard architecture (Extended Industry Standard Architecture, EISA) bus, among others. The bus 1003 may be classified as an address bus, a data bus, a control bus, or the like. For ease of illustration, the bus 1003 in the figures of the present application is not limited to only one bus or one type of bus.
The embodiment of the application provides a computer readable storage medium, wherein computer executing instructions are stored in the computer readable storage medium, and the computer executing instructions are used for realizing the infusion pump control method of the method embodiment when being executed by a processor.
The computer readable storage medium described above may be implemented by any type or combination of volatile or nonvolatile memory devices such as Static Random Access Memory (SRAM), electrically erasable programmable read-only memory (EEPROM), erasable programmable read-only memory (EPROM), programmable read-only memory (PROM), read-only memory (ROM), magnetic memory, flash memory, magnetic or optical disk. A readable storage medium can be any available medium that can be accessed by a general purpose or special purpose computer.
An exemplary readable storage medium is coupled to the processor such the processor can read information from, and write information to, the readable storage medium. In the alternative, the readable storage medium may be integral to the processor. The processor and the readable storage medium may reside in an application specific integrated circuit (Application Specific Integrated Circuits, ASIC for short). The processor and the readable storage medium may reside as discrete components in a device.
Embodiments of the present application provide a computer program product, including a computer program, which when executed by a processor implements the infusion pump control method provided in any of the embodiments of the present application.
Other embodiments of the present application will be apparent to those skilled in the art from consideration of the specification and practice of the invention disclosed herein. This application is intended to cover any variations, uses, or adaptations of the application following, in general, the principles of the application and including such departures from the present disclosure as come within known or customary practice within the art to which the application pertains. It is intended that the specification and examples be considered as exemplary only, with a true scope and spirit of the application being indicated by the following claims.
It is to be understood that the present application is not limited to the precise arrangements and instrumentalities shown in the drawings, which have been described above, and that various modifications and changes may be effected without departing from the scope thereof. The scope of the application is limited only by the appended claims.

Claims (11)

1. An infusion pump control method, characterized by being applied to an infusion pump, the infusion pump comprising: the infusion pump control method comprises the following steps of:
Acquiring first user information through the authentication information acquisition module;
acquiring stored user authority information;
and determining display information output by the display module according to the acquired first user information and user authority information.
2. The method of claim 1, wherein the user permission information includes user identification information and an infusion pump viewing permission, and the determining the display information output by the display module according to the acquired first user information and the user permission information includes:
acquiring an infusion pump checking authority corresponding to the first user information from the user authority information according to the received first user information and the user authority information;
and outputting display information corresponding to the checking authority of the infusion pump on the display module.
3. The method according to claim 2, wherein the display information includes display contents and display modes, and the outputting, on the display module, display information corresponding to the viewing authority of the infusion pump includes:
determining corresponding display content and display modes according to the checking authority of the infusion pump;
Determining display information according to the display content and the display mode;
and outputting the display information on the display module.
4. The infusion pump control method according to claim 2, wherein the user authority information further includes infusion pump operation authority information, the infusion pump control method further comprising:
and judging that the operation instruction input by the user does not meet the corresponding operation authority according to the received first user information and the user authority information, and outputting prompt information and/or not executing the operation item corresponding to the operation instruction.
5. The infusion pump control method according to claim 4, wherein the user authority information further includes operation authority authentication information, the infusion pump control method further comprising:
receiving an operation instruction input by a user;
confirming an authentication mode of the received operation instruction according to the received first user information and user authority information;
and outputting prompt information and/or not executing operation items corresponding to the operation instruction if the authority authentication fails according to the determined authentication mode.
6. The infusion pump control method of claim 1, wherein the authentication information acquisition module comprises one or more of a biometric information acquisition module, a near field communication recognition module, an image recognition module, a voice recognition module.
7. An infusion pump control method, characterized by being applied to an infusion pump, the infusion pump comprising: the infusion pump control method comprises the following steps of:
acquiring first user information through the authentication information acquisition module;
acquiring stored user authority information;
receiving an operation request of the user through the input module;
and judging that the operation request does not meet the operation authority according to the acquired first user information and user authority information, and outputting prompt information and/or not executing operation processing corresponding to the operation instruction through the output module.
8. The infusion pump control method according to claim 7, wherein the user authority information includes user identification information, infusion pump operation authority information.
9. An infusion device comprising: a processor, a memory having code stored therein, the processor executing the code stored in the memory to perform the infusion pump control method of any one of claims 1-6 or 7-8.
10. A computer readable storage medium, wherein computer executable instructions are stored in the computer readable storage medium, which when executed by a processor are adapted to implement the infusion pump control method according to any one of claims 1-6 or 7-8.
11. A computer program product comprising a computer program which, when executed by a processor, implements the infusion pump control method of any one of claims 1-6 or 7-8.
CN202310336389.6A 2023-03-24 2023-03-24 Infusion pump control method, infusion apparatus, and storage medium Pending CN116421817A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN202310336389.6A CN116421817A (en) 2023-03-24 2023-03-24 Infusion pump control method, infusion apparatus, and storage medium

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN202310336389.6A CN116421817A (en) 2023-03-24 2023-03-24 Infusion pump control method, infusion apparatus, and storage medium

Publications (1)

Publication Number Publication Date
CN116421817A true CN116421817A (en) 2023-07-14

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