Transfusion monitoring management method and related equipment

Abstract

According to the infusion monitoring management method and the related equipment, centralized monitoring, quantitative management and standard service of infusion are achieved, and a nurse is timely alarmed to remind a patient of the abnormal situation of infusion. The method comprises the following steps: monitoring weight data of liquid contained in each infusion bottle in N infusion bottles in real time, wherein N is an integer greater than or equal to 1; determining standard weight data and starting time corresponding to a target infusion bottle, wherein the target infusion bottle is any one infusion bottle in the N infusion bottles; according to the standard weight data, the starting moment and the liquid weight data of the target infusion bottle at the current moment, attribute data of the target infusion bottle at the current moment are determined, and the attribute data comprise the instant infusion dripping speed and remaining data of the target infusion bottle; the residual data comprises residual liquid amount and residual duration; judging whether the attribute data accords with a preset alarm rule or not; if yes, a first alarm prompt is sent to medical staff.

Description

Technical Field

[0001] The present invention relates to the medical field, and in particular to an infusion monitoring and management method and related equipment. Background Art

[0002] Intravenous infusion has become one of the most important clinical treatment measures and the most commonly used technical operation. Under the current extremely high infusion rate, there is heavy workload for nurses, anxiety for patients and their families, and high infusion risks.

[0003] At present, the traditional way for patients and their families to monitor infusion is to visually determine the remaining amount of infusion fluid and notify medical staff to change it. This not only involves the energy of patients and their families, increases the mental pressure of patients and their families, and prevents patients from getting a better rest, but also increases the burden on family human resources. When the calls are dense, nurses are unable to cope with them in time, which may cause venous blood return to block the needle, requiring re-venipuncture, increasing the pain of patients, and some may cause infusion risks.

[0004] Therefore, it is urgent to provide an infusion monitoring and management method to monitor and manage the entire infusion process of the patient. Summary of the invention

[0005] The embodiment of the present invention provides an infusion monitoring management method and related equipment, which realizes centralized monitoring, quantitative management and standardized services of infusion, monitors the infusion situation on behalf of the patient, and promptly alerts the nurse to abnormal infusion situations of the patient.

[0006] A first aspect of the present invention provides an infusion monitoring and management method, comprising:

[0007] Real-time monitoring of the liquid weight data contained in each of N infusion bottles, where N is an integer greater than or equal to 1;

[0008] Determine the standard weight data and starting time corresponding to a target infusion bottle, wherein the target infusion bottle is any one of the N infusion bottles;

[0009] Determine attribute data of the target infusion bottle at the current moment according to the standard weight data, the starting time and the liquid weight data of the target infusion bottle at the current moment, wherein the attribute data includes the instantaneous infusion dripping rate and remaining data of the target infusion bottle, and the remaining data includes the remaining liquid volume and the remaining time;

[0010] Determining whether the attribute data conforms to a preset alarm rule;

[0011] If the attribute data meets the preset alarm rule, a first alarm prompt is sent to the medical staff.

[0012] A second aspect of the present invention provides an infusion monitoring and management device, comprising:

[0013] A monitoring module, used for real-time monitoring of the weight data of the liquid contained in each of N infusion bottles, wherein N is an integer greater than or equal to 1;

[0014] A first determination module is used to determine the standard weight data and the starting time corresponding to the target infusion bottle, wherein the target infusion bottle is any one of the N infusion bottles;

[0015] A second determination module is used to determine the attribute data of the target infusion bottle at the current moment according to the standard weight data, the starting time and the liquid weight data of the target infusion bottle at the current moment, wherein the attribute data includes the instantaneous infusion dripping rate and the remaining data of the target infusion bottle, and the remaining data includes the remaining liquid volume and the remaining time;

[0016] A judgment module, used to judge whether the attribute data conforms to a preset alarm rule;

[0017] The alarm module is used to send a first alarm prompt to medical personnel if the attribute data meets the preset alarm rules.

[0018] In a possible design, the judgment module is specifically used for:

[0019] Determine whether the instant infusion drip rate is within the target drip rate interval corresponding to the target infusion bottle, and determine whether the remaining data is less than a preset threshold;

[0020] If the instant infusion drip rate is within the target drip rate interval and the remaining liquid volume is greater than the preset threshold, it is determined that the attribute data does not meet the preset alarm rule;

[0021] If the instant infusion dripping rate is not within the target dripping rate interval, or the remaining liquid volume is less than the preset threshold, it is determined that the attribute data meets the preset alarm rule.

[0022] In a possible design, the alarm module is also used for:

[0023] Generate a target infusion chart of the target infusion bottle in a graphical manner according to the instant infusion dripping rate and the remaining data, and display the target infusion chart;

[0024] After sending the first alarm prompt to the medical staff, determining whether a feedback instruction or an instruction to replace the target infusion bottle is received within a preset response time;

[0025] If the feedback instruction is not received, or the replacement instruction is not received, the instant infusion dripping rate is adjusted according to the remaining liquid volume.

[0026] In a possible design, the alarm module is also used for:

[0027] Real-time monitoring of the adjusted remaining liquid volume of the target infusion bottle after adjusting the instant infusion drip rate;

[0028] If the adjusted remaining liquid volume is lower than the limit liquid volume, the instant infusion drip rate of the target infusion bottle is adjusted to 0, and a second alarm prompt is sent to other medical staff and the user corresponding to the target infusion bottle.

[0029] In a possible design, the alarm module is specifically used for:

[0030] Determining the location information of the target infusion bottle;

[0031] Determine whether the target user corresponding to the target infusion bottle has completed the infusion;

[0032] If yes, sending the first alarm prompt to the medical staff according to the location information;

[0033] If not, the remaining infusion drugs of the target user are determined, and the first alarm prompt is issued to the medical staff according to the identification of the remaining infusion drugs and the location information.

[0034] In a possible design, the first determining module is specifically configured to:

[0035] Acquire medical data of a target user corresponding to the target infusion bottle;

[0036] determining the standard weight data according to the medical data;

[0037] Receive the starting time corresponding to the target infusion bottle input by the medical staff.

[0038] In a possible design, the alarm module is specifically used for:

[0039] Acquire all infusion data of the target user, including infusion drugs, waiting time for replacement of infusion bottles, adjustment of instant infusion drip rate information, start time, end time and infusion duration of the infusion drugs;

[0040] An infusion report for the target user is generated according to all the infusion data, and the infusion report is sent to the target user.

[0041] A third aspect of the present invention provides an electronic device, comprising a memory and a processor, wherein the processor is used to implement the steps of the infusion monitoring management method as described in the first aspect when executing a computer management program stored in the memory.

[0042] A fourth aspect of the present invention provides a computer-readable storage medium having a computer management program stored thereon, which, when executed by a processor, implements the steps of the infusion monitoring and management method as described in the first aspect above.

[0043] In summary, it can be seen that in the embodiment provided by the present invention, by determining the weight data of the liquid remaining in the infusion bottle, the standard weight data and the starting time, and then determining the attribute data of the infusion bottle at the current time according to the standard weight data, the starting time and the liquid weight data of the infusion bottle at the current time, the attribute data includes the instantaneous infusion drip rate and the remaining data of the infusion bottle, and the remaining data includes the remaining liquid volume and the remaining time; judging whether the attribute data meets the preset alarm rules; if the attribute data meets the preset alarm rules, the first alarm prompts the medical staff. In this way, centralized monitoring, quantitative management and standardized services of infusion can be realized without changing the original infusion method, and the infusion situation can be monitored on behalf of the patient, and the nurse can be promptly alerted to abnormal infusion situations of the patient, providing a safe and efficient working environment for medical workers. BRIEF DESCRIPTION OF THE DRAWINGS

[0044] Figure 1 A schematic diagram of a flow chart of an infusion monitoring and management method provided by an embodiment of the present invention;

[0045] Figure 2 A virtual structural diagram of an infusion monitoring and management device provided by an embodiment of the present invention;

[0046] Figure 3 A schematic diagram of the hardware structure of the infusion monitoring and management device provided by an embodiment of the present invention;

[0047] Figure 4 A schematic diagram of an electronic device according to an embodiment of the present invention;

[0048] Figure 5 A schematic diagram of an embodiment of a computer-readable storage medium provided for an embodiment of the present invention. DETAILED DESCRIPTION

[0049] The following will be combined with the drawings in the embodiments of the present invention to clearly and completely describe the technical solutions in the embodiments of the present invention. Obviously, the described embodiments are only part of the embodiments of the present invention, not all of the embodiments. Based on the embodiments of the present invention, all other embodiments obtained by those skilled in the art without creative work are within the scope of protection of the present invention.

[0050] In the following description, specific embodiments of the present invention will be described with reference to steps and symbols performed by one or more computers, unless otherwise stated. Therefore, these steps and operations will be mentioned several times as being performed by a computer, and computer execution referred to herein includes operations by a computer processing unit of electronic signals representing data in a structured form. This operation converts the data or maintains it at a location in the computer's memory system, which can be reconfigured or otherwise change the operation of the computer in a manner familiar to testers in the field. The data structure maintained by the data is a physical location in the memory, which has specific characteristics defined by the data format. However, the principles of the present invention are described in the above text, which does not represent a limitation, and testers in the field will understand that the various steps and operations described below can also be implemented in hardware.

[0051] The principles of the present invention operate with many other general or special purpose computing, communication environments or configurations. Examples of well-known computing systems, environments and configurations suitable for use with the present invention may include, but are not limited to, handheld phones, personal computers, servers, multiprocessor systems, microcomputer-based systems, mainframe computers, and distributed computing environments, including any of the above systems or devices.

[0052] The terms "first", "second", and "third" in the present invention are used to distinguish different objects rather than to describe a specific order. In addition, the terms "include", "have", and any variations thereof are intended to cover non-exclusive inclusions.

[0053] The infusion monitoring and management method provided by the present invention is described below from the perspective of an infusion monitoring and management device. The infusion monitoring and management device may be a server or a service unit in a server, and is not specifically limited.

[0054] See also Figure 1 , Figure 1 A flow chart of an infusion monitoring and management method provided in an embodiment of the present invention, the infusion monitoring and management method comprising:

[0055] 101. Monitor the liquid weight data contained in each of N infusion bottles in real time.

[0056] In this embodiment, a sensor is set on the hook corresponding to the infusion bottle, and the infusion monitoring management device detects the liquid weight data in each of the N infusion bottles in real time through the infusion monitor set on the hook, where N is an integer greater than or equal to 1. That is, when the user performs an infusion, the infusion bottle is hung on the hook, and the infusion monitor set on the hook can monitor the amount of liquid remaining in the infusion bottle. Thus, the infusion monitoring management device can obtain the liquid weight data contained in each of the N infusion bottles monitored in real time by the infusion monitor. The liquid weight data can be expressed in grams or milliliters, which is not specifically limited.

[0057] It should be noted that the infusion monitor supports wireless charging IoT sensors, which can monitor the actual weight of the infusion bag or infusion bottle in real time, and transmit the collected weight data to Blue Bridge via Bluetooth. Blue Bridge then uploads the data to the infusion monitoring and management device via wireless LAN.

[0058] 102. Determine the standard weight data corresponding to the target infusion bottle at the starting time.

[0059] In this embodiment, the infusion monitoring and management device can determine the standard weight data and starting time corresponding to the target infusion bottle, wherein the standard weight data refers to the weight of the liquid contained in the target infusion bottle when it is unopened, and the starting time is the time when the liquid in the target infusion bottle is injected into the user's body, and the target infusion bottle is any one of the N infusion bottles. Specifically, the infusion monitoring and management device can interact with the hospital's HIS system to obtain the medical data of the target user, and the target user is the user corresponding to the target infusion bottle, and the medical data includes but is not limited to the treatment information, medication information and doctor's order information of the target user; then, the standard weight information corresponding to the target infusion bottle can be determined based on the medication information, and the starting time can be the starting time input by the medical staff, or it can be the time when the liquid in the target infusion bottle starts to decrease obtained by the sensor, and there is no specific limitation.

[0060] It should be noted that, through step 101, the liquid weight data contained in each of the N infusion bottles can be monitored in real time, and through step 102, the standard weight data and the starting time can be determined. However, there is no restriction on the order of execution between these two steps. Step 101 can be executed first, or step 102 can be executed first, or they can be executed at the same time, without specific limitation.

[0061] 103. Determine the attribute data of the target infusion bottle at the current moment according to the standard weight data, the starting time, and the liquid weight data of the target infusion bottle at the current moment.

[0062] In this embodiment, the infusion monitoring and management device can determine the attribute data of the target infusion bottle at the current moment based on the standard weight data, the starting time, and the liquid weight data of the target infusion bottle at the current moment, wherein the attribute data includes the instantaneous infusion dripping rate and the remaining data of the target infusion bottle, and the remaining data includes the remaining liquid volume and the remaining time; that is, after determining the marked weight data and the liquid weight data at the current moment, the infusion monitoring and management device subtracts the standard weight data from the current liquid weight data to obtain the liquid weight consumed by the target infusion bottle, determines the dripping time corresponding to the target infusion bottle based on the starting time and the current moment, and then calculates the average dripping rate, and estimates the remaining time required for the target infusion bottle to be completely consumed based on the liquid weight data at the current moment and the average dripping rate.

[0063] It should be noted that the instant infusion speed may be the average dripping speed of the target infusion bottle from the starting time to the current time, or may be the average dripping speed within the current period (eg, 1 minute), subject to specific restrictions.

[0064] 104. Determine whether the attribute data meets the preset alarm rules. If so, execute step 105.

[0065] In this embodiment, after determining the attribute data of the target infusion bottle, the infusion monitoring and management device can determine whether the attribute data meets the preset alarm rules. Specifically, the infusion monitoring and management device determines whether the instant infusion drip rate is in the target drip rate interval corresponding to the target infusion bottle, and determines whether the remaining data is less than the preset threshold value; if the instant infusion drip rate is in the target drip rate interval, and the remaining liquid volume is greater than the preset threshold value, it is determined that the attribute data does not meet the preset alarm rules; if the instant infusion drip rate is not in the target drip rate interval, or the remaining liquid volume is less than the preset threshold value, it is determined that the attribute data meets the preset alarm rules. For example, the target drip rate interval is 20-70 drops / minute, and the preset threshold value is 10ML, then when the instant infusion drip rate is 20-70 drops / minute, it is determined that the instant infusion drip rate does not meet the preset alarm rules, and when the instant infusion drip rate is not 20-70 drops / minute, it is determined that the instant infusion drip rate meets the preset alarm rules; the same is true for the remaining liquid volume. When the remaining liquid volume is less than or equal to 10ML, it is determined that the preset alarm rules are met, otherwise, it is not met.

[0066] 105. Send a first alarm prompt to medical personnel.

[0067] In this embodiment, when the infusion monitoring and management device determines that the attribute data meets the preset alarm rules, it can send a first alarm prompt to the medical staff according to the attribute data. Specifically, it can first determine the location information of the target infusion bottle, that is, the specific location information of the target user's infusion, and judge whether the target user has completed the infusion. If so, the first alarm prompt is issued according to the location information, that is, when it is determined that the target infusion bottle is the last bottle of infusion of the target user, it is only necessary to issue an alarm prompt based on the location information of the target user and the information that the target user's infusion is completed, that is, the first alarm prompt carries the location information and the information that the target user's infusion is completed; if not, it means that the target user still has remaining drugs, and data is interacted with the HIS system to determine the remaining infusion drugs of the target user, and an alarm prompt is issued based on the identification and location information of the remaining infusion drugs, that is, the first alarm prompt carries the location information and the identification of the remaining drugs, so that the medical staff can move to the location of the target user in time to replace the drugs for the target user.

[0068] In one embodiment, the infusion monitoring and management device further performs the following operations:

[0069] Generate a target infusion chart of the target infusion bottle in a graphical manner according to the instant infusion dripping rate and the remaining data, and display the target infusion chart;

[0070] After sending the first alarm prompt to the medical staff, determining whether a feedback instruction or an instruction to replace the target infusion bottle is received within a preset response time;

[0071] If the feedback instruction is not received, or the replacement instruction is not received, the instant infusion dripping rate is adjusted according to the remaining liquid volume.

[0072] In this embodiment, after obtaining the instantaneous infusion dripping rate and the remaining data at the current moment, the infusion monitoring management device can generate a target infusion icon of a target infusion bottle or a target user in the form of an icon, and display the target infusion icon to the medical staff (for example, it can be displayed on a handheld PDA or a large screen of a PC of the medical staff);

[0073] In addition, after the infusion monitoring device sends the first alarm prompt to the medical staff, in order to avoid the medical staff's untimely response, resulting in failure to replace the infusion bottle for the target user or terminate the infusion in time, the timing can be started from the time the first alarm prompt is issued. When the timing time reaches the preset response time, if no feedback instruction or target infusion bottle replacement instruction is received, the immediate infusion drip rate is adjusted according to the remaining liquid volume. For example, the original immediate infusion drip rate is reduced from 30 drops / minute to 10 drops / minute, so as to avoid blood reflux problems caused by the medical staff's untimely response and failure to replace or terminate the infusion.

[0074] It should be noted that the infusion monitoring device can monitor in real time the adjusted remaining liquid volume of the target infusion bottle after adjusting the immediate infusion dripping rate; if the adjusted remaining liquid volume is lower than the limit liquid volume, the immediate infusion dripping rate of the target infusion bottle is adjusted to 0 (which will also completely stop dripping), and send a second alarm prompt to other medical staff (different from the medical staff) and the user corresponding to the target infusion bottle. In this way, when one medical staff is busy, a spare medical staff can be activated.

[0075] It should also be noted that after the target user completes the infusion, the infusion monitoring and management device can obtain all infusion data of the target user, including but not limited to infusion drugs, waiting time for replacement of infusion bottles, adjustment of instant infusion drip rate information (including the adjustment time, the drip rate before adjustment and the drip rate after adjustment), the start time, end time and infusion duration of the infusion drugs (the infusion duration includes the total duration and the infusion duration of each infusion drug), generate an infusion report of the target user based on all the infusion data, and send the infusion report to the target user.

[0076] In summary, it can be seen that in the embodiment provided by the present invention, by determining the weight data of the liquid remaining in the infusion bottle, the standard weight data and the starting time, and then determining the attribute data of the infusion bottle at the current time according to the standard weight data, the starting time and the liquid weight data of the infusion bottle at the current time, the attribute data includes the instantaneous infusion drip rate and the remaining data of the infusion bottle, and the remaining data includes the remaining liquid volume and the remaining time; judging whether the attribute data meets the preset alarm rules; if the attribute data meets the preset alarm rules, the first alarm prompts the medical staff. In this way, centralized monitoring, quantitative management and standardized services of infusion can be realized without changing the original infusion method, and the infusion situation can be monitored on behalf of the patient, and the nurse can be promptly alerted to abnormal infusion situations of the patient, providing a safe and efficient working environment for medical workers.

[0077] The above describes the embodiment of the present invention from the perspective of the infusion monitoring and management method. The following describes the embodiment of the present invention from the perspective of the infusion monitoring and management device.

[0078] See also Figure 2 , a virtual structural diagram of an infusion monitoring and management device according to an embodiment of the present invention, the infusion monitoring and management device 200 comprises:

[0079] A monitoring module 201, for real-time monitoring of the weight data of the liquid contained in each of N infusion bottles, wherein N is an integer greater than or equal to 1;

[0080] A first determination module 202 is used to determine the standard weight data and the starting time corresponding to the target infusion bottle, wherein the target infusion bottle is any one of the N infusion bottles;

[0081] The second determination module 203 is used to determine the attribute data of the target infusion bottle at the current moment according to the standard weight data, the starting time and the liquid weight data of the target infusion bottle at the current moment, wherein the attribute data includes the instant infusion dripping speed and the remaining data of the target infusion bottle, and the remaining data includes the remaining liquid volume and the remaining time;

[0082] A judgment module 204 is used to judge whether the attribute data meets the preset alarm rules;

[0083] The alarm module 205 is used to send a first alarm prompt to medical personnel if the attribute data meets the preset alarm rule.

[0084] In a possible design, the determination module 204 is specifically used for:

[0085] Determine whether the instant infusion drip rate is within the target drip rate interval corresponding to the target infusion bottle, and determine whether the remaining data is less than a preset threshold;

[0086] If the instant infusion drip rate is within the target drip rate interval and the remaining liquid volume is greater than the preset threshold, it is determined that the attribute data does not meet the preset alarm rule;

[0087] If the instant infusion dripping rate is not within the target dripping rate interval, or the remaining liquid volume is less than the preset threshold, it is determined that the attribute data meets the preset alarm rule.

[0088] In a possible design, the alarm module 205 is further used for:

[0089] Generate a target infusion chart of the target infusion bottle in a graphical manner according to the instant infusion dripping rate and the remaining data, and display the target infusion chart;

[0090] After sending the first alarm prompt to the medical staff, determining whether a feedback instruction or an instruction to replace the target infusion bottle is received within a preset response time;

[0091] If the feedback instruction is not received, or the replacement instruction is not received, the instant infusion dripping rate is adjusted according to the remaining liquid volume.

[0092] In a possible design, the alarm module 205 is further used for:

[0093] Real-time monitoring of the adjusted remaining liquid volume of the target infusion bottle after adjusting the instant infusion drip rate;

[0094] If the adjusted remaining liquid volume is lower than the limit liquid volume, the instant infusion drip rate of the target infusion bottle is adjusted to 0, and a second alarm prompt is sent to other medical staff and the user corresponding to the target infusion bottle.

[0095] In a possible design, the alarm module 205 is specifically used for:

[0096] Determining the location information of the target infusion bottle;

[0097] Determine whether the target user corresponding to the target infusion bottle has completed the infusion;

[0098] If yes, sending the first alarm prompt to the medical staff according to the location information;

[0099] If not, the remaining infusion drugs of the target user are determined, and the first alarm prompt is issued to the medical staff according to the identification of the remaining infusion drugs and the location information.

[0100] In a possible design, the first determining module 202 is specifically configured to:

[0101] Acquire medical data of a target user corresponding to the target infusion bottle;

[0102] determining the standard weight data according to the medical data;

[0103] Receive the starting time corresponding to the target infusion bottle input by the medical staff.

[0104] In a possible design, the alarm module 205 is specifically used for:

[0105] Acquire all infusion data of the target user, including infusion drugs, waiting time for replacement of infusion bottles, adjustment of instant infusion drip rate information, start time, end time and infusion duration of the infusion drugs;

[0106] An infusion report for the target user is generated according to all the infusion data, and the infusion report is sent to the target user.

[0107] above Figure 2 The infusion monitoring management device in the embodiment of the present invention has been described from the perspective of modular functional entities. The infusion monitoring management device in the embodiment of the present invention is described in detail from the perspective of hardware processing. Please refer to FIG. 300, which is a schematic diagram of an embodiment of the infusion monitoring management device 300 in the embodiment of the present invention. The infusion monitoring management device 300 includes:

[0108] An input device 301, an output device 302, a processor 303 and a memory 304 (the number of the processor 303 can be one or more, Figure 3 In some embodiments of the present invention, the input device 301, the output device 302, the processor 303 and the memory 304 may be connected via a communication bus or other means, wherein: Figure 3 The communication bus connection is taken as an example.

[0109] Wherein, by calling the operation instruction stored in the memory 304, the processor 303 is used to perform the following steps:

[0110] Real-time monitoring of the liquid weight data contained in each of N infusion bottles, where N is an integer greater than or equal to 1;

[0111] Determine the standard weight data and starting time corresponding to a target infusion bottle, wherein the target infusion bottle is any one of the N infusion bottles;

[0112] Determine attribute data of the target infusion bottle at the current moment according to the standard weight data, the starting time and the liquid weight data of the target infusion bottle at the current moment, wherein the attribute data includes the instantaneous infusion dripping rate and remaining data of the target infusion bottle, and the remaining data includes the remaining liquid volume and the remaining time;

[0113] Determining whether the attribute data conforms to a preset alarm rule;

[0114] If the attribute data meets the preset alarm rule, a first alarm prompt is sent to the medical staff.

[0115] By calling the operation instructions stored in the memory 304, the processor 303 is also used to execute Figure 1 Any method in the corresponding embodiment.

[0116] See also Figure 4 , Figure 4 A schematic diagram of an electronic device according to an embodiment of the present invention.

[0117] like Figure 4 As shown, an embodiment of the present invention provides an electronic device, including a memory 410, a processor 420, and a computer program 411 stored in the memory 410 and executable on the processor 420. When the processor 420 executes the computer program 411, the following steps are implemented:

[0118] Real-time monitoring of the liquid weight data contained in each of N infusion bottles, where N is an integer greater than or equal to 1;

[0119] Determine the standard weight data and starting time corresponding to a target infusion bottle, wherein the target infusion bottle is any one of the N infusion bottles;

[0120] Determine attribute data of the target infusion bottle at the current moment according to the standard weight data, the starting time and the liquid weight data of the target infusion bottle at the current moment, wherein the attribute data includes the instantaneous infusion dripping rate and remaining data of the target infusion bottle, and the remaining data includes the remaining liquid volume and the remaining time;

[0121] Determining whether the attribute data conforms to a preset alarm rule;

[0122] If the attribute data meets the preset alarm rule, a first alarm prompt is sent to the medical staff.

[0123] In the specific implementation process, when the processor 420 executes the computer program 411, it can achieve Figure 1 Any implementation manner in the corresponding embodiments.

[0124] Since the electronic device introduced in this embodiment is a device used to implement an infusion monitoring and management device in the embodiment of the present invention, based on the method introduced in the embodiment of the present invention, technical personnel in this field can understand the specific implementation method of the electronic device of this embodiment and its various variations. Therefore, how the electronic device implements the method in the embodiment of the present invention will not be described in detail here. As long as the equipment used by technical personnel in this field to implement the method in the embodiment of the present invention falls within the scope of protection of the present invention.

[0125] Please refer to Figure 500, which is a schematic diagram of an embodiment of a computer-readable storage medium provided by an embodiment of the present invention.

[0126] As shown in Figure 500, the embodiment of the present invention further provides a computer-readable storage medium 600, on which a computer program 511 is stored. When the computer program 511 is executed by a processor, the following steps are implemented:

[0127] Real-time monitoring of the liquid weight data contained in each of N infusion bottles, where N is an integer greater than or equal to 1;

[0128] Determine the standard weight data and starting time corresponding to a target infusion bottle, wherein the target infusion bottle is any one of the N infusion bottles;

[0129] Determine attribute data of the target infusion bottle at the current moment according to the standard weight data, the starting time and the liquid weight data of the target infusion bottle at the current moment, wherein the attribute data includes the instantaneous infusion dripping rate and remaining data of the target infusion bottle, and the remaining data includes the remaining liquid volume and the remaining time;

[0130] Determining whether the attribute data conforms to a preset alarm rule;

[0131] If the attribute data meets the preset alarm rule, a first alarm prompt is sent to the medical staff.

[0132] In the specific implementation process, the computer program 511 is executed by the processor to achieve Figure 1 Any implementation manner in the corresponding embodiments.

[0133] It should be noted that in the above embodiments, the description of each embodiment has its own emphasis, and for parts that are not described in detail in a certain embodiment, reference can be made to the relevant descriptions of other embodiments.

[0134] Those skilled in the art will appreciate that embodiments of the present invention may be provided as methods, systems, or computer program products. Therefore, the present invention may take the form of a complete hardware embodiment, a complete software embodiment, or an embodiment combining software and hardware. Moreover, the present invention may take the form of a computer program product implemented on one or more computer-usable storage media (including but not limited to disk storage, CD-ROM, optical storage, etc.) containing computer-usable program code.

[0135] The present invention is described with reference to flowcharts and / or block diagrams of methods, devices (systems), and computer program products according to embodiments of the present invention. It should be understood that each process and / or block in the flowchart and / or block diagram, as well as the combination of processes and / or blocks in the flowchart and / or block diagram, can be implemented by computer program instructions. These computer program instructions can be provided to a processor of a general-purpose computer, a special-purpose computer, an embedded computer, or other programmable data processing device to generate a machine, so that the instructions executed by the processor of the computer or other programmable data processing device generate instructions for implementing the processes in the flowchart and / or block diagram. Figure 1 A process or multiple processes and / or boxes Figure 1 A device that provides the functions specified in a block or multiple blocks.

[0136] These computer program instructions may also be stored in a computer-readable memory capable of directing a computer or other programmable data processing device to operate in a specific manner, so that the instructions stored in the computer-readable memory produce an article of manufacture comprising an instruction device, which implements the process Figure 1 A process or multiple processes and / or boxes Figure 1 A function specified in one or more boxes.

[0137] These computer program instructions can also be loaded onto a computer or other programmable data processing device so that a series of operating steps are executed on the computer or other programmable device to produce a computer-implemented process, thereby providing instructions for implementing the process. Figure 1 A process or multiple processes and / or boxes Figure 1 The steps for the functions specified in one or more boxes.

[0138] The embodiment of the present invention also provides a computer program product, which includes computer software instructions. When the computer software instructions are executed on a processing device, the processing device executes the following Figure 1 The process in the corresponding embodiment.

[0139] The computer program product includes one or more computer instructions. When the computer program instructions are loaded and executed on a computer, the process or function described in the embodiment of the present invention is generated in whole or in part. The computer may be a general-purpose computer, a special-purpose computer, a computer network, or other programmable device. The computer instructions may be stored in a computer-readable storage medium, or transmitted from one computer-readable storage medium to another computer-readable storage medium. For example, the computer instructions may be transmitted from one website site, computer, server or data center to another website site, computer, server or data center by wired (e.g., coaxial cable, optical fiber, digital subscriber line (DSL)) or wireless (e.g., infrared, wireless, microwave, etc.) means. The computer-readable storage medium may be any available medium that a computer can store or a data storage device such as a server or data center that includes one or more available media integrated. The available medium may be a magnetic medium (e.g., a floppy disk, a hard disk, a tape), an optical medium (e.g., a DVD), or a semiconductor medium (e.g., a solid state disk (SSD)), etc.

[0140] Those skilled in the art can clearly understand that, for the convenience and brevity of description, the specific working processes of the systems, devices and units described above can refer to the corresponding processes in the aforementioned method embodiments and will not be repeated here.

[0141] In the several embodiments provided by the present invention, it should be understood that the disclosed systems, devices and methods can be implemented in other ways. For example, the device embodiments described above are only schematic. For example, the division of the units is only a logical function division. There are other division methods in actual implementation. For example, multiple units or components can be combined or integrated into another system, or some features can be ignored or not executed. Another point is that the mutual coupling or direct coupling or communication connection shown or discussed can be an indirect coupling or communication connection through some interfaces, devices or units, which can be electrical, mechanical or other forms.

[0142] The units described as separate components may or may not be physically separated, and the components shown as units may or may not be physical units, that is, they may be located in one place or distributed on multiple network units. Some or all of the units may be selected according to actual needs to achieve the purpose of the solution of this embodiment.

[0143] In addition, each functional unit in each embodiment of the present invention may be integrated into one processing unit, or each unit may exist physically separately, or two or more units may be integrated into one unit. The above-mentioned integrated unit may be implemented in the form of hardware or in the form of software functional units.

[0144] If the integrated unit is implemented in the form of a software functional unit and sold or used as an independent product, it can be stored in a computer-readable storage medium. Based on this understanding, the technical solution of the present invention is essentially or the part that contributes to the prior art or all or part of the technical solution can be embodied in the form of a software product. The computer software product is stored in a storage medium, including several instructions for a computer device (which can be a personal computer, a server, or a network device, etc.) to perform all or part of the steps of the method described in each embodiment of the present invention. The aforementioned storage medium includes: U disk, mobile hard disk, read-only memory (ROM), random access memory (RAM), disk or optical disk and other media that can store program codes.

[0145] As described above, the above embodiments are only used to illustrate the technical solutions of the present invention, rather than to limit the same. Although the present invention has been described in detail with reference to the aforementioned embodiments, those skilled in the art should understand that the technical solutions described in the aforementioned embodiments may still be modified, or some of the technical features thereof may be replaced by equivalents. However, these modifications or replacements do not deviate the essence of the corresponding technical solutions from the spirit and scope of the technical solutions of the embodiments of the present invention.

Claims

1. A method for monitoring and managing infusion, characterized in that: include: Real-time monitoring of the liquid weight data contained in each of N infusion bottles, where N is an integer greater than or equal to 1; Determine the standard weight data and starting time corresponding to a target infusion bottle, wherein the target infusion bottle is any one of the N infusion bottles; Determine attribute data of the target infusion bottle at the current moment according to the standard weight data, the starting time and the liquid weight data of the target infusion bottle at the current moment, wherein the attribute data includes the instantaneous infusion dripping rate and remaining data of the target infusion bottle, and the remaining data includes the remaining liquid volume and the remaining time; Determining whether the attribute data conforms to a preset alarm rule; If the attribute data meets the preset alarm rule, a first alarm prompt is sent to the medical staff.

2. The method according to claim 1, characterized in that The determining whether the attribute data meets the preset alarm rules includes: Determine whether the instant infusion drip rate is within the target drip rate interval corresponding to the target infusion bottle, and determine whether the remaining data is less than a preset threshold; If the instant infusion drip rate is within the target drip rate interval and the remaining liquid volume is greater than the preset threshold, it is determined that the attribute data does not meet the preset alarm rule; If the instant infusion dripping rate is not within the target dripping rate interval, or the remaining liquid volume is less than the preset threshold, it is determined that the attribute data meets the preset alarm rule.

3. The method according to claim 1, characterized in that The method further comprises: Generate a target infusion chart of the target infusion bottle in a graphical manner according to the instant infusion dripping rate and the remaining data, and display the target infusion chart; After sending the first alarm prompt to the medical staff, determining whether a feedback instruction or an instruction to replace the target infusion bottle is received within a preset response time; If the feedback instruction is not received, or the replacement instruction is not received, the instant infusion dripping rate is adjusted according to the remaining liquid volume.

4. The method according to claim 3, characterized in that The method further comprises: Real-time monitoring of the adjusted remaining liquid volume of the target infusion bottle after adjusting the instant infusion drip rate; If the adjusted remaining liquid volume is lower than the limit liquid volume, the instant infusion drip rate of the target infusion bottle is adjusted to 0, and a second alarm prompt is sent to other medical staff and the user corresponding to the target infusion bottle.

5. The method according to any one of claims 1 to 4, characterized in that The sending of the first alarm prompt to the medical staff includes: Determining the location information of the target infusion bottle; Determine whether the target user corresponding to the target infusion bottle has completed the infusion; If yes, sending the first alarm prompt to the medical staff according to the location information; If not, the remaining infusion drugs of the target user are determined, and the first alarm prompt is issued to the medical staff according to the identification of the remaining infusion drugs and the location information.

6. The method according to any one of claims 1 to 4, characterized in that The determination of the standard weight data and the starting time corresponding to the target infusion bottle includes: Acquire medical data of a target user corresponding to the target infusion bottle; determining the standard weight data according to the medical data; Receive the starting time corresponding to the target infusion bottle input by the medical staff.

7. The method according to claim 6, characterized in that The method further comprises: Acquire all infusion data of the target user, including infusion drugs, waiting time for replacement of infusion bottles, adjustment of instant infusion drip rate information, start time, end time and infusion duration of the infusion drugs; An infusion report for the target user is generated according to all the infusion data, and the infusion report is sent to the target user.

8. An infusion monitoring and management device, characterized in that: include: A monitoring module, used for real-time monitoring of the weight data of the liquid contained in each of N infusion bottles, wherein N is an integer greater than or equal to 1; A first determination module is used to determine the standard weight data and the starting time corresponding to the target infusion bottle, wherein the target infusion bottle is any one of the N infusion bottles; A second determination module is used to determine the attribute data of the target infusion bottle at the current moment according to the standard weight data, the starting time and the liquid weight data of the target infusion bottle at the current moment, wherein the attribute data includes the instantaneous infusion dripping rate and the remaining data of the target infusion bottle, and the remaining data includes the remaining liquid volume and the remaining time; A judgment module, used to judge whether the attribute data conforms to a preset alarm rule; The alarm module is used to send a first alarm prompt to medical personnel if the attribute data meets the preset alarm rules.

9. An electronic device, characterized in that: include: A memory and a processor, wherein the processor is used to implement the infusion monitoring and management method as described in any one of claims 1 to 7 when executing a computer management program stored in the memory.

10. A computer-readable storage medium having a computer management program stored thereon, characterized in that: When the computer management program is executed by the processor, the infusion monitoring and management method as described in any one of claims 1 to 7 is implemented.

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