Drug infusion adjustment method, device and drug infusion equipment

Abstract

This application discloses a drug infusion adjustment method, device, drug infusion equipment, drug infusion analysis method, drug infusion analysis system, and drug infusion control device. The method comprises: obtaining user medication feedback information and infusion execution information within a preset time interval; determining that the drug infusion settings are unreasonable based on the user's medication feedback information and infusion execution information, and outputting drug infusion adjustment information.

Description

Technical Field

[0001] The present application relates to the field of smart medical technology, for example, to a drug infusion adjustment method, device, drug infusion equipment, drug infusion analysis method, drug infusion analysis system and drug infusion control device. Background Art

[0002] Infusion devices are widely used in the field of clinical medicine. Currently, before performing an infusion, medical workers need to set predetermined infusion parameters on the infusion device.

[0003] In the related art, there is a problem of unreasonable infusion parameter settings. Summary of the Invention

[0004] The present application provides a drug infusion adjustment method, device, drug infusion equipment, drug infusion analysis method, drug infusion analysis system and drug infusion control device to solve the problem of unreasonable infusion parameter setting.

[0005] According to one aspect of the present application, a method for regulating drug infusion is provided, comprising:

[0006] Obtaining medication feedback and infusion execution information from users within a preset time interval;

[0007] Based on the user's medication feedback information and infusion execution information, it is determined that the medication infusion setting is unreasonable, and medication infusion adjustment information is output.

[0008] According to another aspect of the present application, a drug infusion adjustment device is provided, comprising:

[0009] A user information acquisition module is configured to acquire medication feedback information and infusion execution information of the user within a preset time interval;

[0010] The adjustment information determination module is configured to determine whether the drug infusion setting is unreasonable based on the user's medication feedback information and infusion execution information, and output drug infusion adjustment information.

[0011] According to another aspect of the present application, a drug infusion device is provided, comprising:

[0012] a housing, an infusion path at least partially disposed in the housing, a drive device, an input device, an output device, at least one processor; and

[0013] a memory communicatively connected to the at least one processor; wherein,

[0014] The memory stores a computer program that can be executed by the at least one processor, and the computer program is executed by the at least one processor so that the at least one processor can execute the drug infusion adjustment method described in any embodiment of the present application.

[0015] According to another aspect of the present application, a drug infusion analysis method is provided, comprising:

[0016] Obtain one or more of the user's medication feedback information, infusion execution information, and auxiliary analysis information within a set time interval;

[0017] The infusion analysis result is determined based on one or more of the user's medication feedback information, infusion execution information, and auxiliary analysis information within the set time interval.

[0018] According to another aspect of the present application, a drug infusion analysis system is provided, comprising:

[0019] At least one processor executes the drug infusion analysis method described in any embodiment of the present application.

[0020] According to another aspect of the present application, a drug infusion control device is provided, comprising the drug infusion analysis system described in any embodiment of the present application. BRIEF DESCRIPTION OF THE DRAWINGS

[0021] The following is a brief introduction to the drawings required for the description of the embodiments. The drawings described below are only some embodiments of the present application. For ordinary technicians in this field, other drawings can be obtained based on these drawings without any creative work.

[0022] Figure 1 This is a flow chart of a drug infusion adjustment method provided in accordance with Example 1 of the present application;

[0023] Figure 2 This is a flow chart of a drug infusion regulation method provided in Example 2 of the present application;

[0024] Figure 3 is a schematic diagram of an infusion parameter adjustment method provided in Example 2 of the present application;

[0025] Figure 4 This is a schematic structural diagram of a drug infusion regulating device provided in accordance with Example 3 of the present application;

[0026] Figure 5 This is a flow chart of a drug infusion analysis method provided in Example 4 of the present application;

[0027] Figure 6This is a schematic structural diagram of a drug infusion analysis system provided according to Example 5 of the present application;

[0028] Figure 7 1 is a schematic structural diagram of a drug infusion control device provided according to Example 6 of the present application;

[0029] Figure 8 It is a structural diagram of an electronic device for implementing the drug infusion adjustment method of an embodiment of the present application. DETAILED DESCRIPTION

[0030] In order to help those skilled in the art better understand this application, the following will clearly and completely describe the embodiments of this application in conjunction with the drawings in the embodiments of this application. The described embodiments are only part of the embodiments of this application. Based on the embodiments in this application, all other embodiments obtained by ordinary technicians in this field without making creative efforts should fall within the scope of protection of this application.

[0031] It should be noted that the acquisition, storage, use, processing, etc. of data in the technical solution of the present application all comply with the relevant provisions of national laws and regulations. The terms "target", "original", etc. in the specification and claims of the present application and the above-mentioned drawings are used to distinguish similar objects and are not necessarily used to describe a specific order or sequential order. It should be understood that the data used in this way can be interchangeable under appropriate circumstances, so that the embodiments of the present application described herein can be implemented in an order other than those illustrated or described herein. In addition, the terms "including" and "having" and any of their variations are intended to cover non-exclusive inclusions, for example, a process, method, system, product or equipment comprising a series of steps or units is not necessarily limited to those steps or units clearly listed, but may include other steps or units that are not clearly listed or inherent to these processes, methods, products or equipment.

[0032] Example 1

[0033] Figure 1 This is a flowchart of a drug infusion adjustment method provided in Example 1 of the present application. This embodiment is applicable to the case of intelligently adjusting the parameters of an infusion device. The method can be executed by a drug infusion adjustment device, which can be implemented in the form of hardware and / or software. The drug infusion adjustment device can be configured in a terminal, for example, the terminal can be an infusion device. Figure 1 As shown, the method includes:

[0034] S110: Obtaining medication feedback information and infusion execution information of the user within a preset time interval.

[0035] S120: Determine that the drug infusion setting is unreasonable based on the user's medication feedback information and infusion execution information, and output drug infusion adjustment information.

[0036] In this embodiment, medication feedback information refers to feedback information generated by the user during the medication process, and may include user physiological parameter information, medication requirement information, etc., wherein the user may be a patient receiving infusion therapy. Infusion execution information refers to parameter information used by the infusion device to execute infusion to the user, and may include one or more of real-time infusion parameters and historical infusion parameters. Real-time infusion parameters may include one or more of medication type, dosage, used dosage, amount to be used, infusion speed, infusion progress, infusion duration, etc., and historical infusion parameters may include one or more of medication type, infusion volume, infusion time, infusion duration, etc. An infusion device refers to a device that integrates a control device, infusion pipeline, drive device, etc. The various devices or components in the infusion device may be arranged on the same body or in a distributed configuration. The various devices or components may be connected via wired or wireless communication methods, such as WIFI, Bluetooth, etc.

[0037] In some embodiments, a parameter collection device can be used to collect physiological parameter information of the user within a preset time interval. For example, the parameter collection device can be a sensor, and optionally can include one or more of a heart rate sensor, a blood oxygen sensor, a blood pressure sensor, an electrocardiogram collection device, an end-tidal carbon dioxide collection device, and a fetal heart rate collection device, so as to collect information such as the user's heart rate, blood oxygen, blood pressure and electrocardiogram, end-tidal carbon dioxide and fetal heart rate. In some embodiments, the user can input medication requirement information through input devices such as buttons, keyboards, voice recognition devices, and gesture recognition devices of the infusion device. The preset time interval can be a time interval set by the user, the user's family, a doctor, or an administrator, and can be set according to actual needs, such as the time interval corresponding to a single infusion or the set duration corresponding to multiple infusions.

[0038] In this embodiment, after obtaining the user's medication feedback information and infusion execution information within a preset time interval, the rationality of the medication infusion settings can be determined based on the user's medication feedback information and infusion execution information within the preset time interval, thereby adjusting unreasonable medication infusion settings. Medication infusion adjustment information can be generated based on the user's medication feedback information and infusion execution information. The medication infusion adjustment information can be guidance information for adjusting medication infusion or information for adjusting infusion device control parameters. Optionally, the medication infusion adjustment information can include infusion parameter adjustment information, infusion parameter setting information, and medication adjustment information. The infusion parameter adjustment information is used to increase or decrease the infusion parameters based on the original infusion parameters, for example, increasing the infusion speed based on the original infusion speed. The infusion parameter setting information is used to set the infusion parameters to the parameter values ​​corresponding to the infusion parameter setting information, for example, the user directly setting the infusion speed value. The medication adjustment information is used to adjust the infusion of medication, for example, adjusting the medication dosage.

[0039] Based on the above embodiment, the step of determining whether the drug infusion setting is unreasonable based on the user's medication feedback information and infusion execution information includes:

[0040] Get pre-configured medication determination rules;

[0041] It is determined that the drug infusion setting is unreasonable based on the pre-configured medication determination rule and the user's medication feedback information and infusion execution information.

[0042] The medication determination rule may be a pre-configured threshold condition rule.

[0043] In one embodiment, the medication feedback information and the infusion execution information may be compared with the threshold conditions in the medication determination rules. If the medication feedback information and the infusion execution information comply with the medication determination rules, the medication infusion setting is determined to be reasonable; if the medication feedback information and the infusion execution information do not comply with the medication determination rules, the medication infusion setting is determined to be unreasonable.

[0044] Based on the above embodiment, after outputting the drug infusion adjustment information, the method further includes at least one of the following steps: storing the drug infusion adjustment information in a data storage module; and sending the drug infusion adjustment information to a target device.

[0045] The data storage module may be a data storage device within the infusion device, configured to store data locally. The target device may be a device that is communicatively connected to the infusion device, such as a remote cloud server or a healthcare terminal. Optionally, the target device may be configured to display medication infusion adjustment information.

[0046] Exemplarily, the drug infusion adjustment information is sent to a cloud server, and then the drug infusion adjustment information is sent to a medical terminal through the cloud server; wherein the medical terminal is used to receive and display the drug infusion adjustment information, and the staff can adjust the infusion parameters of the infusion device according to the drug infusion adjustment information on the medical terminal, and send the infusion parameters to the infusion device, thereby achieving the purpose of telemedicine.

[0047] The medical terminal refers to a terminal device that allows medical workers to view or operate infusion parameters. For example, the medical terminal can be a personal computer or tablet computer. The cloud server is connected to the medical terminal and the drug infusion device, and can store and forward drug infusion adjustment information.

[0048] In some embodiments, the user's infusion control reference information may also be obtained, a user portrait may be generated based on the infusion control reference information, and infusion parameter adjustment information of the current infusion user may be determined based on the user portrait.

[0049] Exemplarily, the infusion control reference information may include one or more of the user's physical parameters (including one or more of height, weight, age, etc.), physiological parameters, medical history, doctor's orders, infusion medications, and infusion parameters. Each infusion control reference information is converted into a user profile element in multiple feature dimensions to generate a user profile for the user, wherein the user profile may include multiple profile elements, each of which may include at least one tag field. Optionally, corresponding infusion parameter adjustment information may be matched in a data profile library based on the tag fields in the user profile, wherein the data profile library may also include infusion parameter adjustment information corresponding to multiple tag fields.

[0050] The embodiment of the present application obtains the user's medication feedback information and infusion execution information within a preset time interval, and judges that the drug infusion setting is unreasonable based on the user's medication feedback information and infusion execution information, and outputs drug infusion adjustment information. This realizes the judgment of unreasonable drug infusion setting and can feedback the drug infusion adjustment information, providing a basis for adjusting the infusion parameters, thereby solving the problem of unreasonable infusion parameter setting.

[0051] Example 2

[0052] Figure 2This is a flow chart of a drug infusion adjustment method provided in Example 2 of the present application. The method of this embodiment can be combined with the various optional schemes in the drug infusion adjustment method provided in the above embodiments. The drug infusion adjustment method provided in this embodiment has been modified. Optionally, the method also includes: obtaining auxiliary analysis information; accordingly, the step of determining the drug infusion adjustment information based on the user's medication feedback information and infusion execution information includes: judging that the drug infusion setting is unreasonable based on the auxiliary analysis information, the user's medication feedback information and infusion execution information, and outputting the drug infusion adjustment information; wherein, the auxiliary analysis information includes one or more of the user type, user physical information, user disease information, user medical history and infusion drug information.

[0053] like Figure 2 As shown, the method includes:

[0054] S210: Obtaining medication feedback information and infusion execution information of the user within a preset time interval.

[0055] S220: Obtain auxiliary analysis information.

[0056] S230: Determine that the drug infusion setting is unreasonable based on the auxiliary analysis information, the user's medication feedback information, and the infusion execution information, and output drug infusion adjustment information.

[0057] In this embodiment, auxiliary analysis information refers to information used to assist in determining whether drug infusion settings are unreasonable, and may include one or more of the following: user type, user physical information, user disease information, user medical history, and infused drug information. User type refers to the type of patient undergoing the infusion. User physical information may include one or more of height, weight, and age. User disease information may include information on one or more diseases suffered by the user. User medical history refers to the user's historical medical records. Infused drug information may include information such as the type of drug infused by the user and the dosage of the drug.

[0058] In one embodiment, auxiliary analysis information is retrieved from a database based on a user identifier. It is understood that utilizing this auxiliary analysis information can enrich the basis for unreasonable judgments, thereby improving the accuracy of the judgment results. The user identifier refers to a unique identifier used to identify a user, such as a user ID or account number.

[0059] Based on the above embodiment, after outputting the drug infusion adjustment information, the method further includes: generating a medication analysis report based on one or more of the auxiliary analysis information, the user's medication feedback information, and infusion execution information.

[0060] The medication analysis report is used to summarize various related information about the current user, including auxiliary analysis information, the user's medication feedback information, and infusion execution information. The auxiliary analysis information, the user's medication feedback information, and the infusion execution information can be analyzed to obtain the user's medication infusion report. It can be understood that the medication analysis report can quickly understand the patient's medication status and thus improve the user's plan.

[0061] Based on the above embodiment, after outputting the drug infusion adjustment information, the method further includes at least one of the following steps:

[0062] establishing a correspondence between the drug infusion information and the user based on the drug infusion adjustment information;

[0063] Based on the drug infusion adjustment information, a corresponding relationship between the drug infusion information and the auxiliary analysis information is established.

[0064] The drug infusion information refers to parameter information associated with drug infusion, which may include infusion parameters of the infusion device, drug-related information, etc.

[0065] In some embodiments, a correspondence between the drug infusion information and a user identifier representing the user can be established based on the drug infusion adjustment information. In some embodiments, a correspondence between the drug infusion information and auxiliary analysis information can be established based on the drug infusion adjustment information. After the correspondence is established, continuous quality improvement (CQI) can be performed based on the correspondence.

[0066] Based on the above embodiment, the medication feedback information includes at least one of medication requirement information and physiological parameter information.

[0067] Among them, the medication demand information may include the number of presses, the frequency of presses, and the duration of presses. In this embodiment, the user can adjust the parameters of the infusion device by pressing the control button, wherein the number of presses refers to the number of times the user presses the control button within a preset time interval, the frequency of presses refers to the frequency of presses of the control button within a preset time interval, and the duration of presses refers to the length of time the user presses the control button. The number of presses, the frequency of presses, and the duration of presses can be used to determine whether the control button press is valid. For example, if the number of presses exceeds the preset number threshold, the current press operation is determined to be an invalid press, otherwise, it is a valid press; similarly, if the press frequency exceeds the preset frequency threshold, the current press operation is determined to be an invalid press, otherwise, it is a valid press; if the press duration exceeds the preset duration threshold, the current press operation is determined to be an invalid press, otherwise, it is a valid press. Physiological parameter information may include blood oxygen, blood pressure, heart rate, end-tidal carbon dioxide, fetal heart rate, etc.

[0068] For example, Figure 3 As shown, medication guidance suggestions (i.e., drug infusion adjustment information) are generated based on the number of effective presses, the number of invalid presses, medical orders, historical medication information, physiological parameter information, and basic patient information. The medication guidance suggestions are then sent to the cloud platform (i.e., cloud server) through the network module. The cloud platform then sends the medication guidance suggestions to the terminal device of the medical worker (i.e., medical terminal). The staff can adjust the infusion parameters of the infusion device according to the medication guidance suggestions on the medical terminal, and send the infusion parameters to the infusion device.

[0069] The embodiments of the present application can enrich the basis for unreasonable judgments by utilizing auxiliary analysis information, thereby improving the accuracy of the judgment results.

[0070] Example 3

[0071] Figure 4 This is a schematic diagram of the structure of a drug infusion regulating device provided in Example 3 of this application. Figure 4 As shown, the device includes:

[0072] The user information acquisition module 310 is configured to acquire the user's medication feedback information and infusion execution information within a preset time interval;

[0073] The adjustment information determination module 320 is configured to determine that the drug infusion setting is unreasonable based on the user's medication feedback information and infusion execution information, and output drug infusion adjustment information.

[0074] In some optional embodiments, the apparatus is further configured to perform at least one of the following steps:

[0075] Storing the drug infusion adjustment information in a data storage module;

[0076] The drug infusion adjustment information is sent to a target device.

[0077] In some optional embodiments, the target device is used to display the drug infusion adjustment information.

[0078] In some optional implementations, the adjustment information determination module 320 is further configured to:

[0079] Get pre-configured medication determination rules;

[0080] It is determined that the drug infusion setting is unreasonable based on the pre-configured medication determination rule and the user's medication feedback information and infusion execution information.

[0081] In some optional embodiments, the device is further configured to:

[0082] Obtain auxiliary analysis information;

[0083] Accordingly, the adjustment information determination module 320 is further configured to:

[0084] determining that the drug infusion setting is unreasonable based on the auxiliary analysis information, the user's medication feedback information, and the infusion execution information, and outputting drug infusion adjustment information;

[0085] The auxiliary analysis information includes one or more of user type, user physical information, user disease information, user medical history and infusion drug information.

[0086] In some optional embodiments, the device is further configured to:

[0087] A medication analysis report is generated based on one or more of the auxiliary analysis information, the user's medication feedback information, and the infusion execution information.

[0088] In some optional embodiments, the apparatus is further configured to perform at least one of the following steps:

[0089] establishing a correspondence between the drug infusion information and the user based on the drug infusion adjustment information;

[0090] Based on the drug infusion adjustment information, a corresponding relationship between the drug infusion information and the auxiliary analysis information is established.

[0091] In some optional embodiments, the medication feedback information includes at least one of medication requirement information and physiological parameter information.

[0092] The drug infusion adjustment device provided in the embodiments of the present application can execute the drug infusion adjustment method provided in any embodiment of the present application, and has the corresponding functional modules and beneficial effects of the execution method.

[0093] Example 4

[0094] Figure 5 This is a flowchart of a drug infusion analysis method provided in Example 4 of the present application. This embodiment is applicable to the case of automatically analyzing patient medication. The method can be executed by a drug infusion analysis system. The drug infusion analysis system can be implemented in the form of hardware and / or software. The drug infusion analysis system can be configured in a terminal. Figure 5 As shown, the method includes:

[0095] S410: Obtain one or more of the user's medication feedback information, infusion execution information, and auxiliary analysis information within a set time interval.

[0096] S420: Determine an infusion analysis result based on one or more of the user's medication feedback information, infusion execution information, and auxiliary analysis information within the set time interval.

[0097] In this embodiment, the auxiliary analysis information may include alarm type, alarm parameters, department, user type, user physical information, user disease information, user medical history, etc. Among them, the alarm type refers to the alarm type for infusion abnormality, which may include abnormal infusion rate, abnormal blood reflux, etc.; the alarm parameter refers to the alarm data or alarm number; the department refers to the department where the user is treated; the user type is the type of patient receiving infusion; the user's physical information may include one or more information such as height, weight and age; the user's disease information may include information on one or more diseases suffered by the user; the user's medical history refers to the user's historical medical record information. Medication feedback information refers to the feedback information generated by the user during the medication process, which may include user physiological parameter information, medication demand information, etc., wherein the user may be a patient receiving infusion treatment. Infusion execution information refers to the parameter information of the infusion device executing the infusion to the user, which may include one or more real-time infusion parameters and historical infusion parameters. The real-time infusion parameters may include one or more of the following: medication type, medication dosage, medication dosage already used, medication dosage to be used, infusion speed, infusion progress, infusion duration, etc. The historical infusion parameters may include one or more of the following: medication type, infusion volume, infusion time, infusion duration, etc. The infusion device refers to a device that integrates a control device, infusion pipeline, drive device, etc. The various devices or components in the infusion device may be arranged on the same body or in a distributed configuration. The various devices or components may be connected via wired or wireless communication methods, such as WIFI, Bluetooth, etc.

[0098] It should be noted that the medication feedback information, infusion execution information and auxiliary analysis information can be obtained in a preset manner and / or by a user's choice.

[0099] In some embodiments, a parameter collection device can be used to collect physiological parameter information of the user within a preset time interval. For example, the parameter collection device can be a sensor, and optionally can include one or more of a heart rate sensor, a blood oxygen sensor, a blood pressure sensor, an electrocardiogram collection device, an end-tidal carbon dioxide collection device, and a fetal heart rate collection device, so as to collect information such as the user's heart rate, blood oxygen, blood pressure and electrocardiogram, end-tidal carbon dioxide and fetal heart rate. In some embodiments, the user can input medication requirement information through input devices such as buttons, keyboards, voice recognition devices, and gesture recognition devices of the infusion device. The preset time interval can be a time interval set by the user, the user's family, a doctor, or an administrator, and can be set according to actual needs, such as the time interval corresponding to a single infusion or the set duration corresponding to multiple infusions.

[0100] In some embodiments, auxiliary analysis information can be retrieved from a database based on the user identifier. It is understood that by utilizing the auxiliary analysis information, data can be enriched, thereby improving the accuracy of the infusion analysis results.

[0101] In this embodiment, after obtaining the user's medication feedback information, infusion execution information, and auxiliary analysis information within a set time interval, an infusion analysis result can be determined based on one or more of the medication feedback information, infusion execution information, and auxiliary analysis information. The infusion analysis result refers to the monitoring results of the patient's medication infusion status and can be used to characterize the patient's medication infusion status.

[0102] For example, based on medication feedback information, infusion execution information, alarm type, alarm parameters, department, patient type, physical information, disease information, medical history and other data, statistical analysis is performed from multiple angles to obtain infusion analysis results, and the infusion analysis results are output in the form of a report for display to doctors or patients.

[0103] Based on the above embodiment, after determining the infusion analysis result based on one or more of the user's medication feedback information, infusion execution information and auxiliary analysis information within the set time interval, the method further includes: determining the drug infusion setting based on the infusion analysis result.

[0104] Among them, drug infusion setting refers to the patient's drug infusion plan.

[0105] In some embodiments, the infusion analysis results can be matched against pre-set regimen determination rules to determine drug infusion settings, enabling improvements and recommendations for medication regimens. The regimen determination rules can include multiple sets of infusion analysis results and drug infusion settings, with the infusion analysis results in the regimen determination rules corresponding to the drug infusion settings. In some embodiments, medical personnel can manually formulate a new medication regimen based on the infusion analysis results and set the infusion parameters corresponding to the new medication regimen through the medical terminal.

[0106] Based on the above embodiment, after determining the drug infusion setting based on the infusion analysis result, the method further includes at least one of the following steps: establishing a corresponding relationship between the drug infusion setting and the user; establishing a corresponding relationship between the drug infusion setting and the auxiliary analysis information.

[0107] In some embodiments, a correspondence between medication infusion settings and a user identifier representing a user can be established; in some embodiments, a correspondence between medication infusion settings and auxiliary information can be established. After the correspondence is established, continuous quality improvement (CQI) can be performed based on the correspondence.

[0108] The embodiment of the present application obtains one or more of the user's medication feedback information, infusion execution information, and auxiliary analysis information within a set time interval, and determines the infusion analysis result based on one or more of the user's medication feedback information, infusion execution information, and auxiliary analysis information within the set time interval, thereby providing a basis for adjusting the infusion parameters and solving the problem of unreasonable infusion parameter settings.

[0109] Example 5

[0110] Figure 6 This is a structural diagram of a drug infusion analysis system provided in Example 5 of the present application. The system includes at least one processor that executes the drug infusion analysis method described in any embodiment of the present application.

[0111] In one embodiment, if Figure 6 As shown, the system includes a processor 501 and a memory 502, wherein the memory stores a computer program. The number of the processor 501 in the system can be one or more. Figure 6 A processor 501 is taken as an example;

[0112] The memory 502 is a computer-readable storage medium that can be used to store software programs, computer-executable programs, and modules, such as the program instructions / modules corresponding to the drug infusion analysis method in the embodiments of the present application. The processor 501 executes the software programs, instructions, and modules stored in the memory 502 to perform various functional applications and data processing of the device, that is, to execute a drug infusion analysis method, which includes:

[0113] Obtain one or more of the user's medication feedback information, infusion execution information, and auxiliary analysis information within a set time interval;

[0114] The infusion analysis result is determined based on one or more of the user's medication feedback information, infusion execution information, and auxiliary analysis information within the set time interval.

[0115] Of course, when executing computer program instructions, the processor provided in the embodiment of the present application can also perform relevant operations in the drug infusion analysis method provided in any embodiment of the present application.

[0116] The memory 502 may mainly include a program storage area and a data storage area, wherein the program storage area may store an operating system and at least one application required for a function; the data storage area may store data created based on the use of the terminal, etc. In addition, the memory 502 may include a high-speed random access memory and may also include a non-volatile memory, such as at least one disk storage device, a flash memory device, or other non-volatile solid-state storage device. In some instances, the memory 502 may include a memory remotely located relative to the processor 501, and these remote memories may be connected to the device via a network. Examples of the above-mentioned network include the Internet, an intranet, a local area network, a mobile communication network, and combinations thereof.

[0117] The system also includes an input device 503 and an output device 504; the processor 501, memory 502, input device 503 and output device 504 in the device can be connected through a bus or other means. Figure 6 The bus connection is taken as an example.

[0118] The input device 503 may be used to receive input digital or character information, and generate key signal input related to user settings and function control of the device.

[0119] The output device 504 may include a display device such as a display screen, for example, a display screen of a user terminal.

[0120] Example 6

[0121] Figure 7 This is a structural schematic diagram of a drug infusion control device provided in Example 6 of the present application, wherein the drug infusion control device includes the drug infusion analysis system described in any embodiment of the present application.

[0122] In one embodiment, the drug infusion control device refers to a control device that can control the operation of the infusion device. Based on the drug infusion analysis system, the drug infusion control device can also include a power supply, buttons, communication components, etc.

[0123] Example 7

[0124] Figure 8Shown is a block diagram of a drug infusion device 10 that can be used to implement an embodiment of the present application. The drug infusion device is intended to represent various forms of digital computers, such as laptop computers, desktop computers, workstations, personal digital assistants, servers, blade servers, mainframe computers, and other suitable computers. The drug infusion device can also represent various forms of mobile devices, such as personal digital processing, cellular phones, smart phones, wearable devices (such as helmets, glasses, watches, etc.) and other similar computing devices. The components shown herein, their connections and relationships, and their functions are merely examples and are not intended to limit the implementation of the present application described and / or required herein.

[0125] like Figure 8 As shown, the drug infusion device 10 includes at least one processor 11 and a memory, such as a read-only memory (ROM) 12 or a random access memory (RAM) 13, communicatively connected to the at least one processor 11. The memory stores a computer program executable by the at least one processor. The processor 11 can perform various appropriate actions and processes based on the computer program stored in the ROM 12 or loaded from a storage unit 18 into the RAM 13. The RAM 13 can also store various programs and data required for the operation of the drug infusion device 10. The processor 11, ROM 12, and RAM 13 are interconnected via a bus 14. An input / output (I / O) interface 15 is also connected to the bus 14. In some embodiments, the drug infusion device 10 further includes a housing, an infusion path at least partially disposed within the housing, a drive device, an input device, an output device, and the like.

[0126] Multiple components in the drug infusion device 10 are connected to the I / O interface 15, including an input unit 16, such as a keyboard, a mouse, etc.; an output unit 17, such as various types of displays, speakers, etc.; a storage unit 18, such as a magnetic disk, an optical disk, etc.; and a communication unit 19, such as a network card, a modem, a wireless communication transceiver, etc. The communication unit 19 allows the drug infusion device 10 to exchange information / data with other devices via a computer network such as the Internet and / or various telecommunication networks.

[0127] The processor 11 may be a variety of general and / or specialized processing components with processing and computing capabilities. Some examples of the processor 11 include a central processing unit (CPU), a graphics processing unit (GPU), various dedicated artificial intelligence (AI) computing chips, various processors running machine learning model algorithms, a digital signal processor (DSP), and any appropriate processor, controller, microcontroller, etc. The processor 11 performs the various methods and processes described above, such as a drug infusion adjustment method, which includes:

[0128] Obtaining medication feedback and infusion execution information from users within a preset time interval;

[0129] Based on the user's medication feedback information and infusion execution information, it is determined that the medication infusion setting is unreasonable, and medication infusion adjustment information is output.

[0130] In some embodiments, the medication infusion adjustment method can be implemented as a computer program that is tangibly contained in a computer-readable storage medium, such as the storage unit 18. In some embodiments, part or all of the computer program can be loaded and / or installed on the medication infusion device 10 via the ROM 12 and / or the communication unit 19. When the computer program is loaded into the RAM 13 and executed by the processor 11, one or more steps of the medication infusion adjustment method described above can be performed. Alternatively, in other embodiments, the processor 11 can be configured to perform the medication infusion adjustment method in any other suitable manner (e.g., by means of firmware).

[0131] Various embodiments of the systems and techniques described herein can be implemented in digital electronic circuit systems, integrated circuit systems, field programmable gate arrays (FPGAs), application specific integrated circuits (ASICs), application specific standard parts (ASSPs), system on chips (SOCs), complex programmable logic devices (CPLDs), computer hardware, firmware, software, and / or combinations thereof. These various embodiments can include being implemented in one or more computer programs that can be executed and / or interpreted on a programmable system that includes at least one programmable processor, which can be a special purpose or general purpose programmable processor that can receive data and instructions from a storage system, at least one input device, and at least one output device, and transmit data and instructions to the storage system, the at least one input device, and the at least one output device.

[0132] Computer programs for implementing the methods of the present application may be written in any combination of one or more programming languages. These computer programs may be provided to a processor of a general-purpose computer, a special-purpose computer, or other programmable data processing device, such that when the computer program is executed by the processor, the functions / operations specified in the flowcharts and / or block diagrams are implemented. The computer program may be executed entirely on the machine, partially on the machine, as a stand-alone software package, partially on the machine and partially on a remote machine, or entirely on a remote machine or server.

[0133] In the context of the present application, a computer-readable storage medium can be a tangible medium that can contain or store a computer program for use by an instruction execution system, device or equipment or used in combination with an instruction execution system, device or equipment. A computer-readable storage medium can include an electronic, magnetic, optical, electromagnetic, infrared or semiconductor system, device or equipment, or any suitable combination of the foregoing. Alternatively, a computer-readable storage medium can be a machine-readable signal medium. A machine-readable storage medium can include an electrical connection based on one or more lines, a portable computer disk, a hard disk, a random access memory (RAM), a read-only memory (ROM), an erasable programmable read-only memory (EPROM), a flash memory, an optical fiber, a portable compact disc read-only memory (CD-ROM), an optical storage device, a magnetic storage device, or any suitable combination of the foregoing.

[0134] To provide for user interaction, the systems and techniques described herein can be implemented on a medication infusion device having: a display device (e.g., a CRT (cathode ray tube) or a liquid crystal display (LCD) monitor) for displaying information to the user; and a keyboard and pointing device (e.g., a mouse or trackball) through which the user can provide input to the medication infusion device. Other types of devices can also be used to provide for user interaction; for example, the feedback provided to the user can be any form of sensory feedback (e.g., visual feedback, auditory feedback, or tactile feedback); and input from the user can be received in any form (including acoustic input, voice input, or tactile input).

[0135] The systems and techniques described herein can be implemented in a computing system that includes back-end components (e.g., as a data server), or a computing system that includes middleware components (e.g., an application server), or a computing system that includes front-end components (e.g., a user computer with a graphical user interface or web browser through which a user can interact with embodiments of the systems and techniques described herein), or a computing system that includes any combination of such back-end components, middleware components, or front-end components. The components of the system can be interconnected by any form or medium of digital data communication (e.g., a communication network). Examples of communication networks include: a local area network (LAN), a wide area network (WAN), a blockchain network, and the Internet.

[0136] A computing system may include clients and servers. The clients and servers are typically remote from each other and typically interact via a communication network. This client-server relationship arises through computer programs running on the respective computers, creating a client-server relationship. The server may be a cloud server, also known as a cloud computing server or cloud host. This server is a hosting product within the cloud computing service ecosystem that addresses the management difficulties and limited scalability of traditional physical hosting and VPS services.

[0137] It should be understood that the various forms of the processes shown above can be used to reorder, add, or delete steps. For example, the steps described in this application can be performed in parallel, sequentially, or in a different order, as long as the desired results of the technical solutions of this application can be achieved.

Claims

1. A drug infusion regulating device, used for: Obtaining medication feedback information and infusion execution information from a user within a preset time interval; the user's medication feedback information includes medication need information and physiological parameter information, and the medication need information includes the number of presses, the frequency of presses, and the duration of presses; the number of presses, the frequency of presses, and the duration of presses are used to determine whether the control button press is valid; Obtain auxiliary analysis information and pre-configured medication determination rules, including: The auxiliary analysis information includes user type, user physical information, user disease information, user medical history and infusion drug information; determining whether the drug infusion setting is reasonable based on the auxiliary analysis information, the user's medication feedback information, the pre-configured medication determination rule, and the infusion execution information; and outputting drug infusion adjustment information if the drug infusion setting is unreasonable; Among them, the drug infusion adjustment information includes infusion parameter adjustment information; the output of drug infusion adjustment information includes: obtaining the user's infusion control reference information, generating a user portrait based on the infusion control reference information, and determining the infusion parameter adjustment information of the current infusion user based on the user portrait.

2. The apparatus according to claim 1, further configured to perform at least one of the following steps after outputting the drug infusion adjustment information: Storing the drug infusion adjustment information in a data storage module; The drug infusion adjustment information is sent to a target device.

3. The device according to claim 2, wherein The target device is used to display the drug infusion adjustment information.

4. The device according to claim 1, after outputting the drug infusion adjustment information, is further used to: generate a medication analysis report based on one or more of the auxiliary analysis information, the user's medication feedback information and the infusion execution information.

5. The apparatus according to claim 4, further configured to perform at least one of the following steps after outputting the drug infusion adjustment information: establishing a correspondence between the drug infusion information and the user based on the drug infusion adjustment information; Based on the drug infusion adjustment information, a corresponding relationship between the drug infusion information and the auxiliary analysis information is established.

6. A drug infusion regulating device comprising: A user information acquisition module is configured to acquire medication feedback information and infusion execution information of the user within a preset time interval; and obtaining auxiliary analysis information and pre-configured medication determination rules, wherein the user's medication feedback information includes medication demand information and physiological parameter information, the medication demand information includes the number of presses, the frequency of presses, and the duration of presses; the number of presses, the frequency of presses, and the duration of presses are used to determine whether the control button press is effective; wherein the auxiliary analysis information includes user type, user physical information, user disease information, user medical history, and infusion drug information; an adjustment information determination module, configured to determine that the drug infusion setting is unreasonable based on the auxiliary analysis information, the user's medication feedback information, the infusion execution information, and a pre-configured medication determination rule, and output drug infusion adjustment information; Among them, the drug infusion adjustment information includes infusion parameter adjustment information; the adjustment information determination module is configured to specifically obtain the user's infusion control reference information, generate a user portrait based on the infusion control reference information, and determine the infusion parameter adjustment information of the current infusion user based on the user portrait.

7. A drug infusion analysis device, used for: Obtaining medication feedback information, infusion execution information, auxiliary analysis information, and pre-configured medication determination rules from a user within a set time interval; the user's medication feedback information includes medication requirement information and physiological parameter information, the medication requirement information includes the number of presses, the frequency of presses, and the duration of presses; the number of presses, the frequency of presses, and the duration of presses are used to determine whether the control button press is effective; the auxiliary analysis information includes user type, user physical information, user disease information, user medical history, and infusion medication information; Determining an infusion analysis result based on the user's medication feedback information, infusion execution information, auxiliary analysis information, and pre-configured medication determination rules within the set time interval; Determine the drug infusion settings based on the infusion analysis results, so as to output drug infusion adjustment information when the drug infusion settings are unreasonable; wherein, the drug infusion adjustment information includes infusion parameter adjustment information; outputting the drug infusion adjustment information includes: obtaining the user's infusion control reference information, generating a user portrait based on the infusion control reference information, and determining the infusion parameter adjustment information of the current infusion user based on the user portrait.

8. The apparatus according to claim 7, further configured to perform at least one of the following steps after determining a drug infusion setting based on the infusion analysis result: Establishing a correspondence between the drug infusion setting and the user; A correspondence between the drug infusion setting and the auxiliary analysis information is established.

9. A drug infusion analysis system, comprising the drug infusion analysis device according to claim 7 or 8.

10. A drug infusion control device comprising the drug infusion analysis system according to claim 9.

Images