CN115376662A

CN115376662A - Infusion pump, infusion control method thereof and configuration method of infusion scheme

Info

Publication number: CN115376662A
Application number: CN202210551131.3A
Authority: CN
Inventors: 陈剑; 章蕾; 潘瑞玲; 陈嘉欣; 李幽兰; 王成富
Original assignee: Shenzhen Mindray Scientific Co Ltd
Current assignee: Shenzhen Mindray Scientific Co Ltd
Priority date: 2021-05-18
Filing date: 2022-05-18
Publication date: 2022-11-22

Abstract

The application provides an infusion pump, an infusion control method thereof and a configuration method of an infusion scheme, wherein the infusion pump comprises a human-computer interaction device used for outputting information outwards and receiving external input; the memory is used for storing a plurality of infusion schemes and at least one department identifier, and the department identifier and the infusion scheme correspond to each other; wherein the infusion protocol comprises a preset default infusion protocol; the processor is used for controlling the human-computer interaction device to output at least one department identifier, determining a first target identifier according to a first selection instruction when the first selection instruction is triggered, controlling the human-computer interaction device to output at least one infusion scheme according to the first target identifier and the corresponding relation between the department identifier and the infusion scheme, and determining a target infusion scheme according to a second selection instruction when the second selection instruction is triggered. The infusion pump can enable medical personnel to skip the step of setting infusion parameters when in use, and simplifies the operation of the medical personnel.

Description

Infusion pump, infusion control method thereof and configuration method of infusion scheme

Technical Field

The invention relates to the field of medical equipment, in particular to an infusion pump, an infusion control method thereof and a configuration method of an infusion scheme.

Background

In medical work, infusion and injection are very frequent medical behaviors, medical staff need to use a large number of pumps to perform infusion and injection every day, and if the operation is improper, errors are easily set to cause wrong treatment or cause wrong diagnosis, so that a treatment scheme is changed, the treatment effect is influenced, and even a patient is injured.

And the medical staff sets infusion parameters on the pump before using the pump to infuse or inject each time. However, each department, especially general ward, mainly uses the medicine of the special system, such as obstetrics, and the most important medicines are two kinds: tocolytics and tocolytics; the oncology department mainly comprises antitumor drugs, and the small part of the antitumor drugs comprises antiemetic drugs, hormone and the like; the cardiology department is mainly vasoactive, cardiotonic and antiarrhythmic; the respiratory medicine is mainly anti-inflammatory, cough relieving, phlegm eliminating, asthma relieving, vasoactive and heart strengthening medicine; the nephrology department mainly adopts anti-inflammatory, diuretic and kidney-protecting medicines; gynecology is mainly a drug for anti-inflammation and hemostasis. Therefore, the similar departments have obvious universality on the medication mode and the treatment scheme: the types of the common medicines are similar (or consistent), the concentrations of the common medicines are similar (or consistent), and the flow rates of the common medicines are similar (or consistent). On the other hand, the departments have similarities in the configuration management functions related to infusion. For example, neonatal pediatric and pediatric occlusion pressure alarm gears are significantly different from adult departments, but neonatal pediatric or pediatric occlusion pressure alarm gears have respective common ranges.

In response to the above-described characteristics of department administration, pumps currently on the market are not designed to provide the user with ease of operation. Traditional pump usually needs the user to use medicine at every turn and all sets up the parameter one by one, and not only complex operation has also reduced clinical medical care's work efficiency, has increased the risk of maloperation.

Disclosure of Invention

According to a first aspect, there is provided in an embodiment an infusion pump comprising:

the human-computer interaction device is used for outputting information outwards and receiving external input;

the department identification and infusion protocol management system comprises a memory, a database and a management server, wherein the memory is used for storing a plurality of infusion protocols, at least one department identification and a corresponding relation between the department identification and the infusion protocols; wherein the infusion protocol comprises a preset default infusion protocol, each infusion protocol corresponds to one infusion drug, and each department identifier corresponds to one department;

the processor is used for controlling the human-computer interaction device to output at least one department identifier, determining a first target identifier from the at least one department identifier according to a first selection instruction when the triggering of the first selection instruction is detected, controlling the human-computer interaction device to output at least one infusion scheme corresponding to the first target identifier according to the first target identifier and the corresponding relation between the department identifier and the infusion scheme, and determining a target infusion scheme from the at least one infusion scheme corresponding to the first target identifier according to a second selection instruction when the triggering of the second selection instruction is detected.

According to a second aspect, there is provided in an embodiment an infusion pump comprising:

the man-machine interaction device is used for outputting information outwards and receiving external input;

the device comprises a memory, a processor and a memory, wherein the memory is used for storing a plurality of infusion schemes, at least one classification identifier and the corresponding relation between the classification identifier and the infusion scheme; wherein the infusion protocol comprises a preset default infusion protocol, the at least one classification identifying a particular classification used to characterize the infusion protocol;

the processor is used for controlling the human-computer interaction device to output at least one classification identifier, determining a third target identifier from the at least one classification identifier according to a first selection instruction when the triggering of the first selection instruction is detected, controlling the human-computer interaction device to output at least one infusion scheme corresponding to the third target identifier according to the third target identifier and the corresponding relation between the classification identifier and the infusion scheme, and determining a target infusion scheme from the at least one infusion scheme corresponding to the third target identifier according to a second selection instruction when the triggering of the second selection instruction is detected.

According to a third aspect, there is provided in one embodiment an infusion pump comprising:

the system comprises a memory, a database and a database, wherein the memory is used for storing a plurality of configuration management items, at least one department identifier and the corresponding relation between the department identifier and the configuration management items; the configuration management items comprise preset default configuration management items, each configuration management item is used for managing an infusion configuration, and each department identification corresponds to a department;

the processor is used for controlling the human-computer interaction device to output at least one department identifier, determining a first target identifier from the at least one department identifier according to a first selection instruction when the triggering of the first selection instruction is detected, controlling the human-computer interaction device to output at least one configuration management item corresponding to the first target identifier according to the first target identifier and the corresponding relation between the department identifier and the configuration management item, and determining a target configuration management item from the at least one configuration management item corresponding to the first target identifier according to a second selection instruction when the triggering of the second selection instruction is detected.

According to a fourth aspect, there is provided in an embodiment an infusion pump comprising:

the device comprises a memory, a display and a control unit, wherein the memory is used for storing a plurality of department identifications, a plurality of infusion scheme identifications and a plurality of infusion parameters of parameter values to be set, each department identification corresponds to one department, and each infusion scheme identification corresponds to one infusion medicine;

the processor is used for controlling the human-computer interaction device to output a plurality of department identifications, determining a first target identification from the plurality of department identifications according to a first operation instruction when the first operation instruction is triggered, controlling the human-computer interaction device to output a plurality of infusion scheme identifications, determining a second target identification from the plurality of infusion scheme identifications according to a second operation instruction when the second operation instruction is triggered, associating the first target identification with the second target identification to obtain the association relation between the first target identification and the second target identification, controlling the human-computer interaction device to output a plurality of infusion parameters of parameter values to be set, obtaining the setting of the parameter values of the plurality of infusion parameters by a user to form an infusion scheme associated with the second target identification, obtaining the correspondence relation between the first target identification and the infusion scheme according to the association relation between the first target identification and the second target identification, and controlling the memory to store the correspondence relation between the first target infusion identification and the infusion scheme.

According to a fifth aspect, there is provided in an embodiment an infusion pump comprising:

a memory for storing at least one class identifier, a plurality of infusion protocol identifiers, and a plurality of infusion parameters for which parameter values are to be set, the at least one class identifier each being used to characterize a particular class of the infusion protocol;

the processor is used for controlling the human-computer interaction device to output at least one classification identifier, controlling the human-computer interaction device to output a plurality of infusion scheme identifiers according to a third target identifier in the at least one classification identifier when a first operation instruction is triggered, determining a second target identifier in the plurality of infusion scheme identifiers according to a second operation instruction when a second operation instruction is triggered, associating the third target identifier with the second target identifier to obtain an association relation between the third target identifier and the second target identifier, controlling the human-computer interaction device to output at least one infusion parameter, obtaining a setting of a parameter value of the at least one infusion parameter by a user to form an infusion scheme associated with the second target identifier, obtaining a corresponding relation between the third target identifier and the infusion scheme according to the association relation between the third target identifier and the second target identifier, and controlling the memory to store the corresponding relation between the third target identifier and the infusion scheme.

According to a sixth aspect, an embodiment provides an infusion control method of an infusion pump, comprising:

outputting at least one preset department identifier, wherein each department identifier corresponds to one department;

when a first selection instruction is triggered, determining a first target identifier from the at least one department identifier according to the first selection instruction;

outputting at least one infusion scheme corresponding to the first target identifier according to a preset corresponding relation between department identifiers and infusion schemes, wherein the infusion schemes comprise preset default infusion schemes, and each infusion scheme corresponds to one infusion medicine;

when a second selection instruction is detected to be triggered, a target infusion protocol is determined from at least one infusion protocol corresponding to the first target identification according to the second selection instruction.

According to a sixth aspect, there is provided in an embodiment a method of configuring an infusion protocol, comprising:

outputting a plurality of department identifiers stored in advance, and when a first operation instruction is triggered, determining a first target identifier from the department identifiers according to the first operation instruction, wherein each department identifier corresponds to one department;

outputting a plurality of infusion scheme identifications stored in advance, determining a second target identification from the plurality of infusion scheme identifications according to a second operation instruction when the second operation instruction is triggered, and associating the first target identification with the second target identification, wherein each infusion scheme identification corresponds to one infusion drug;

outputting a plurality of prestored infusion parameters of parameter values to be set, acquiring the setting of the user on the parameter values of the plurality of infusion parameters, and forming an infusion scheme associated with the second target identifier;

and obtaining and storing the corresponding relation between the first target identifier and the infusion scheme according to the incidence relation between the first target identifier and the second target identifier.

According to a seventh aspect, an embodiment provides a computer-readable storage medium having a program stored thereon, the program being executable by a processor to implement the above-mentioned method.

The benefits of the above embodiment are:

(1) The infusion pump is initially set, a default infusion scheme can be built in, and medical staff do not need to introduce the infusion scheme from other equipment.

(2) The edited default infusion scheme can be quickly acquired by selecting a department when the medical staff uses the infusion set, so that the complicated steps for setting parameters are reduced.

(3) The healthcare worker may perform maintenance and editing of the infusion protocol directly at the infusion pump end for future use.

Drawings

FIG. 1 is a schematic view of an embodiment of an infusion pump;

FIG. 2 is a display interface of a plurality of department identifiers of an embodiment;

FIG. 3 is a display interface for entering a department identifier of an embodiment;

FIG. 4 is a display interface of a plurality of infusion protocol identifications for an embodiment;

FIG. 5 is a display interface of a plurality of infusion parameters of an embodiment;

FIG. 6 is an operational flow interface of a configuration management item of an embodiment;

FIG. 7 is an operational flow interface for configuring management items of another embodiment;

FIG. 8 is a schematic view of an alarm editing interface of an embodiment;

FIG. 9 is an operational flow interface of a configuration management item of yet another embodiment;

FIG. 10 is an operational flow interface for selecting a target infusion protocol of an embodiment;

FIG. 11 is an embodiment of an operational flow interface for editing quick edit parameters;

FIG. 12 is an operational flow interface for selecting a target parameter value for a fast edit parameter, according to one embodiment;

FIG. 13 is a flow chart of a method of configuring an infusion protocol of an embodiment;

fig. 14 is a flow chart of an infusion control method of an infusion pump of an embodiment.

Detailed Description

The present invention will be described in further detail with reference to the following detailed description and accompanying drawings. Wherein like elements in different embodiments are numbered with like associated elements. In the following description, numerous details are set forth in order to provide a better understanding of the present application. However, those skilled in the art will readily recognize that some of the features may be omitted or replaced with other elements, materials, methods in different instances. In some instances, certain operations related to the present application have not been shown or described in detail in order to avoid obscuring the core of the present application from excessive description, and it is not necessary for those skilled in the art to describe these operations in detail, so that they may be fully understood from the description in the specification and the general knowledge in the art.

Furthermore, the features, operations, or characteristics described in the specification may be combined in any suitable manner to form various embodiments. Also, the various steps or actions in the method descriptions may be transposed or transposed in order, as will be apparent to one of ordinary skill in the art. Thus, the various sequences in the specification and drawings are for the purpose of describing certain embodiments only and are not intended to imply a required sequence unless otherwise indicated where such sequence must be followed.

The ordinal numbers used herein for the components, such as "first," "second," etc., are used merely to distinguish between the objects described, and do not have any sequential or technical meaning. The term "connected" and "coupled" when used in this application, unless otherwise indicated, includes both direct and indirect connections (couplings).

The invention discloses an infusion pump, and fig. 1 shows a hardware structure block diagram of the infusion pump of some embodiments of the invention. The infusion pump includes a human interface device 110, memory 120, a processor 130, RF circuitry 140, a power drive circuit 150, a drop count sensor 160, a bubble sensor 170, a pressure sensor 180, a temperature sensor 190, which communicate via one or more communication buses or signal lines.

The infusion pump may be any medical device that performs an infusion operation as set by a user based on a fluid substance as configured by the user, controllably infusing the configured fluid substance (e.g., medical fluid) into a patient, including, but not limited to, infusion pumps, syringe pumps, and the like. The infusion pump can be used with an infusion set (such as an infusion tube and a syringe). It should be understood that the infusion pump is only one example, and that its components may have more or fewer components than shown, or a different configuration of components. The various components of fig. 1 may be implemented in hardware, software, or a combination of hardware and software, including one or more signal processing and/or application specific integrated circuits.

The human-computer interaction device 110 is used for outputting information and receiving external input, in some embodiments, the human-computer interaction device 110 may be a display screen on the infusion pump, and the display screen may include a touch layer and a display layer which are stacked, and the touch layer provides an input/output interface between the infusion pump and a user; the touch layer may include a resistive screen, a surface acoustic wave screen, an infrared touch screen, an optical touch screen, a capacitive screen, or a nano-film, and is an inductive display device capable of receiving input signals such as a contact. The visual output optionally includes graphics, text, charts, video, and combinations thereof. Some or all of the visual output may correspond to user interface objects.

The display screen may also receive user input based on tactile sensation and/or contact. The touch layer of the display screen forms a touch sensitive surface that receives user input. The touch layer and display controller detect contact (and any movement or interruption of the touch) on the touch layer and translate the detected contact into interaction with user interface objects, such as one or more soft keys, displayed on the touch layer. In one exemplary embodiment, the point of contact between the touch layer and the user corresponds to one or more fingers of the user. The touch layer may use LCD (liquid crystal display) technology or LPD (light emitting polymer display) technology, but in other embodiments other display technologies may be used. The touch layer and display controller may detect contact and movement or break thereof using any of a number of touch sensitive technologies, including but not limited to capacitive, resistive, infrared, and surface acoustic wave technologies, as well as other proximity sensor arrays, or other technologies for determining one or more points of contact with the touch layer.

The memory 120 is used for storing a plurality of department identifications 1, a plurality of infusion protocol identifications 2 and a plurality of infusion parameters of parameter values to be set, wherein each department identification 1 corresponds to a department, and the departments include but are not limited to obstetrics and gynecology, pediatrics, liver surgery and the like; each infusion scheme identifier 2 corresponds to an infusion drug, where the department identifier 1 may be a name, a code, and a customized symbol that can distinguish different departments, for example, the word "cardiology" may be used as one department identifier 1, or a symbol of the heart may be used as the department identifier 1 corresponding to the cardiology, and similarly, the infusion scheme identifier 2 may also be a built-in word or symbol, and hereinafter, the displayed character of the name of the infusion drug is also one of the infusion scheme identifiers 2, and the infusion drug may be various known drugs at present. Infusion parameters refer to parameters that need to be set when configuring or formulating an infusion protocol, or in this way, if the necessary infusion parameter values are set, an infusion protocol can be formed, and the infusion parameters include, but are not limited to, the usual concentration of the drug, the classification of the drug, the usual rate of the drug (flow rate or dosage rate) during treatment, the usual treatment mode of the drug, etc. In some embodiments, the stored infusion parameters may also have predefined default values that the user may directly select for use when configuring the infusion protocol.

The processor 130 drives the power device of the infusion pump through the power driving circuit 150, so that the power device can controllably move, and drives the control object (such as a pump door, a liquid stopping clip, a peristaltic squeezing mechanism or a push-pull box) to move through one or more force transmission/conversion devices (such as gears, transmission shafts, lead screws, nuts or sliders) during the movement. The power plant may be an electromagnetic device that converts or transmits electrical energy according to the laws of electromagnetic induction, such as a Permanent Magnet (PM) motor, a reactive (VR) motor, and a Hybrid (HB) motor. In some embodiments, the motor may move a control object (e.g., a pump door, a liquid stop clip, a pump sheet, or a push-pull box) of the infusion pump, so that the control object achieves a preset movement state.

The RF (radio frequency) circuit 140 receives and transmits electromagnetic waves. The RF circuit 140 converts electrical signals into electromagnetic waves, or vice versa, and communicates with a communication network and other communication devices via electromagnetic waves. The RF circuitry 140 may include well-known circuitry for performing these functions, including but not limited to an antenna system, an RF transceiver, one or more amplifiers, a tuner, one or more oscillators, a CODEC chipset, a Subscriber Identity Module (SIM) card, memory, and so forth. The RF circuitry 140 may communicate with networks and other devices via wireless communications, the networks may be the World Wide Web (WWW), an intranet, and/or a wireless network such as a cellular telephone network, a wireless Local Area Network (LAN), and/or a Metropolitan Area Network (MAN). Wireless communication may use any of a variety of communication standards, protocols, and technologies, including, but not limited to, global system for mobile communications (GSM), enhanced Data GSM Environment (EDGE), wideband Code Division Multiple Access (WCDMA), code Division Multiple Access (CDMA), time Division Multiple Access (TDMA), bluetooth (e.g., IEEE 802.15.1), wireless fidelity (WIFI) (e.g., IEEE802.11a, IEEE802.11 b, IEEE802.11g, and/or IEEE802.11 n), voice over internet protocol (VoIP), wi-MAX, protocols for email, instant messaging, and/or Short Message Service (SMS), or any other suitable communication protocol, including those not yet developed on the filing date herein.

In some embodiments, the drop number sensor 160 is used to detect the drop flow rate or flow in the infusion set.

In some embodiments, one or more bubble sensors 170 are used to detect the presence and magnitude of gas within the infusion set. The bubble sensor 170 may be an ultrasonic sensor or an infrared sensor, etc.

In some embodiments, the pressure sensor 180 may respond to the pressure value of the measured object and convert the pressure value into an electrical signal for detection and send to the processor 130. The pressure sensor may be a resistive strain gauge pressure sensor, a semiconductor strain gauge pressure sensor, a piezoresistive pressure sensor, an inductive pressure sensor, a capacitive pressure sensor, a resonant pressure sensor, a fiber optic pressure sensor, or a capacitive acceleration sensor. In some embodiments, the pressure sensor 180 may be used to detect the internal pressure of the infusion set or the external pressure of the infusion set. In some embodiments, the pressure sensor 180 may also be used to detect the in-situ status of the subject (e.g., an infusion set). In some embodiments, the pressure sensor 180 may detect an occlusion inside the infusion set, or detect if the infusion set is leaking.

The infusion pump may be pre-configured with a department-related infusion protocol before shipping or before being handed to a healthcare worker for use. Specifically, after the infusion pump is turned on, the processor 130 may control the human-computer interaction device 110 to output a plurality of department identifiers 1, and when it is detected that the first operation instruction is triggered, determine, according to the first operation instruction, to determine the first target identifier from the plurality of department identifiers 1.

The triggering mode of the first operation instruction may be various, in some embodiments, after the infusion pump is started, the display screen of the infusion pump pops up the display interface shown in fig. 2, and the user may select the first target identifier by clicking the display screen to trigger the first operation instruction, so as to determine the first target identifier. In other embodiments, as shown in fig. 3, the infusion pump may further support user customization of the first target identifier, that is, inputting the first target identifier may also trigger the first operation instruction, by which the database of department identifiers 1 stored in the memory 120 may be increased, thereby increasing the subsequent selection of departments by the user.

In addition, the processor 130 may further control the human-computer interaction device 110 to output a plurality of infusion protocol identifiers 2, and when it is detected that a second operation instruction is triggered, a second target identifier of the user is determined according to the second operation instruction.

The triggering manner of the second operation instruction may be various, in some embodiments, the display screen of the infusion pump may pop up a display interface as shown in fig. 4, where the infusion protocol identifier 2 is presented by a name of a chinese language of the infusion drug, in other embodiments, the infusion protocol identifier 2 may also be another type of manner that can be understood by the medical staff, for example, the infusion protocol identifier 2 is a latin abbreviation of the infusion drug, and the user may select the second target identifier by clicking the display screen to trigger the second operation instruction, so as to determine the second target identifier, and in fig. 4, a classification label 3 corresponding to the infusion protocol identifier 2 is further provided to help the user to quickly find the corresponding second target identifier, and since the infusion protocol identifier 2 is presented by a name of the infusion drug in fig. 4, the classification label 3 is set based on the type of the infusion drug, and the user may quickly check the infusion drug of the department, the vasoactive type, the sedation type, and analgesia type on the display interface. In other embodiments, the infusion pump may further support user-defined second target identifier, that is, inputting the second target identifier may also trigger the second operation instruction, and the input modes include, but are not limited to, text input, voice input, and input through an external device, for example, the infusion drug may be entered by scanning a bar code of a drug package through a connected bar code, or by photographing the drug package and then recognizing the infusion drug through a recognition algorithm stored in the memory 120, and the above modes may increase the database of the infusion protocol identifier 2 in the memory 120, and when the user wants to configure an infusion protocol corresponding to another department next time, there may be more choices from the database of the infusion protocol identifier 2.

After the first target identifier and the second target identifier are determined, the processor 130 associates the first target identifier with the second target identifier to obtain an association relationship between the first target identifier and the second target identifier, and actually binds the association relationship between the department and the infusion drug under the condition that the second target identifier corresponds to the infusion drug.

After obtaining the association relationship between the first target identifier and the second target identifier, the processor 130 further controls the human-computer interaction device 110 to output at least one infusion parameter, and obtains the setting of the user on the parameter value of the at least one infusion parameter, so as to form an infusion scheme associated with the second target identifier. It should be noted that the term "parameter value" in this application does not only include parameter values in numerical categories, but also includes other types of parameter values, such as displayed text, colors, and various information.

As shown in fig. 5, when the infusion drug corresponding to the second target identifier is selected to be dopamine, the infusion parameter output by the infusion pump is displayed on two switchable display interfaces, because the display screen of the infusion pump is small, the infusion parameter of the infusion pump is displayed on two switchable display interfaces, wherein a user can set the color of the second target identifier, thereby changing the color of the second target identifier in fig. 4, and can also change the drug concentration, the drug classification, whether the drug is a commonly used drug, and the like, which are subsequently displayed on the infusion pump, and it is easy to understand that if the parameter value of the item "whether the drug is a commonly used parameter" is modified to be no, dopamine is not displayed under the classification label 3 "commonly used" in fig. 4. After the user sets the parameter values in fig. 4 and clicks and saves the parameter values, the infusion protocol corresponding to dopamine, which is a medicine, is set.

Since the processor 130 has obtained the association relationship between the first target identifier and the second target identifier, after the configuration of the infusion protocol corresponding to the second target identifier is completed, that is, the infusion protocol is the infusion protocol used in the department corresponding to the first target identifier, that is, the processor 130 may obtain the correspondence relationship between the first target identifier and the infusion protocol, and then the processor 130 stores the correspondence relationship between the first target identifier and the infusion protocol in the memory 120. The above process is a process of configuring an infusion solution for a department, and after the "save" button is clicked in fig. 5, the infusion solution is saved in the memory 120, and if the return button at the upper left corner in fig. 5 is clicked, the display interface shown in fig. 4 is returned, and a second target identifier associated with the first target identifier may be further added to the display interface, so as to add the infusion solution associated with the department corresponding to the first target identifier. After the infusion schemes related to a certain department are configured, the user can return to the display interface shown in fig. 2 to select and configure the infusion scheme required by the department corresponding to the next first target identifier. Through repeated operations, the memory 120 may store a correspondence relationship between a plurality of department identifiers 1 and a plurality of infusion protocols, where each department identifier 1 corresponds to at least one infusion protocol, and infusion protocols corresponding to different department identifiers 1 may be the same or different, for example, both department a and department B have dopamine-related infusion protocols, and infusion parameters of the two infusion protocols may be identical. The correspondence between the department identification 1 and the infusion protocol may be stored in the memory 120 in the form of a mapping table.

In some embodiments, the memory 120 is further configured to store a correspondence between a department identifier 1 and at least one type of configuration management item, the human-computer interaction device 110 may further output a management interface 10 corresponding to the first target identifier, the management interface 10 includes at least one category guidance control 4, each category guidance control 4 is configured to guide the user to complete editing of one type of configuration management item, and one of the configuration management items is an infusion protocol, that is, the infusion protocol may be edited through the management interface 10. For example, when the user selects department identifier 1 corresponding to "department of cardiology" in fig. 2, the human-computer interaction device 110 may output the management interface 10 in fig. 6, wherein three classification guidance controls 4 are disposed on the management interface 10, wherein: the infusion protocol management system comprises a classification guiding control 4 of 'drug management', the classification guiding control 4 is used for guiding a user to finish editing an infusion protocol, when the user clicks 'drug management', the management interface 10 is switched to a first editing interface 20, the first editing interface 20 is similar to the interface shown in the figure 4, the infusion protocol identification 2 is displayed in a mode of infusing a drug name, and the user can trigger a second operation instruction to determine a second target identification through selection operation in the first editing interface 20. In the interface shown in fig. 6, it indicates that the user clicks and selects the infusion scheme identifier 2 of "dopamine" as the second target identifier, then the first editing interface 20 is switched to the second editing interface 30 corresponding to "dopamine", the user can complete editing of the parameter values of the corresponding infusion parameters in the second editing interface 30, the meaning of the contents included in the second editing interface 30 is similar to that in fig. 5, which is not described herein again, and when the user completes editing of the parameter values of the infusion parameters in the second editing interface 30, the configuration of the infusion scheme corresponding to "dopamine" is also completed, and the infusion scheme can be stored in the memory 120; the system also comprises a classification guiding control 4 of 'configuration management', wherein the classification guiding control 4 is used for guiding a user to complete the setting of a configuration management item of alarm parameters, as shown in fig. 7, after the user clicks 'configuration management', a management interface 10 is switched to an alarm editing interface, and the user can complete the editing of the alarm parameters on the alarm editing interface, for example, as shown in fig. 7 and 8, the alarm parameters can be various alarm limit parameters, common alarm limit parameters include but are not limited to blocking pressure, approaching completion time, approaching completion allowance, bubble size, speed soft/hard upper limit, and speed soft/hard lower limit, wherein the speed soft upper limit refers to an upper infusion speed limit which needs to be noticed but can be accepted, the speed hard upper limit refers to an upper infusion speed limit which needs to be noticed but can be accepted, and similarly, the speed soft lower limit refers to a lower infusion speed limit which needs to be noticed but can be accepted, and the speed hard lower limit refers to an infusion speed lower limit which is strictly forbidden; still include this classification of "brand management" and guide control 4, this classification guides control 4 to be used for guiding the user to accomplish the edition of this configuration management item of consumptive material parameter, as shown in fig. 9, after the user clicks "brand management", management interface 10 can switch over to consumptive material editing interface, the consumptive material brand that shows in this consumptive material editing interface in the consumptive material brand storehouse supplies the user to select, consumptive material class parameter is used for the brand that the infusion medicine adopted, can prestore the consumptive material brand storehouse that obtains through research for the user to select.

From the above description, it can be seen that the present application provides a series of interactive modes for facilitating parameter setting on an infusion pump, and through the ideas of classification guidance and step-by-step setting, a user can conveniently and rapidly complete editing of various configuration management items of an infusion scheme.

It can be seen from the above embodiments that the infusion pump in the present application supports configuration of an infusion protocol and binding between departments and the infusion protocol on the pump, and can select a department or an infusion drug directly from a database, or create a new department by a user himself or add a new type of infusion drug by various means, create a new drug library, and edit various types of configuration management items.

In some embodiments, the infusion protocol may not be matched with the department, and specifically, the department identifier 1 is not stored in the memory 120, but is a category identifier, at least one category identifier is used to characterize a specific category of the infusion protocol, for example, the specific category is a patient type, a hospital type, etc., similar to the department identifier 1, the user needs to first determine a third target identifier from the at least one category identifier, and then set a parameter value of an infusion parameter of the corresponding infusion protocol, so that one or more infusion protocols are added under the third target identifier, and the correspondence between the plurality of category identifiers and the infusion protocols can be obtained through multiple operations.

Having described configuring the infusion protocol and how the first target identifier is related to the infusion protocol, the following describes how a healthcare worker uses the infusion pump of the present application.

When the infusion pump storing the correspondence between the department identifier 1 and the infusion protocol is delivered to the hands of the medical staff for use, it is first necessary to determine which department the infusion pump is to be used in.

In some embodiments, after the infusion pump is turned on, the medical staff may enter a display interface for department selection, a department identifier 1 corresponding to a department for which an infusion scheme has been configured is displayed in the display interface for department selection, and the medical staff may select the first target identifier according to a need thereof, for example, the display interface shown in fig. 1 is displayed.

In addition, the infusion pump may determine in which department the infusion pump is to be used by itself through other manners, in some embodiments, the medical staff needs to input identity information of themselves or use an ID card with the identity information to use the infusion pump, so the processor 130 may further determine in which department the infusion pump is to be used currently by obtaining the identity information of the medical staff, in other embodiments, when the infusion pump is used, the identity information of the patient is usually required to be entered, and the infusion pump may further determine in which department the patient is located currently according to the identity information of the patient, so as to determine in which department the infusion pump is to be used; the infusion pump can also establish the relevance with the medical orders or establish the relevance with the PDA to determine departments; when the infusion pump is installed in a particular department, power must also be supplied, etc., and the processor 130 can determine which department it is located in based on which interface in the hospital it is connected to.

After determining the department, the processor 130 may control the human-computer interaction device 110 to output at least one infusion protocol corresponding to the first target identifier according to the correspondence between the department identifier 1 and the infusion protocol stored in the memory 120. In some embodiments, when the user selects the department of cardiology, the display screen of the infusion pump may display a left display interface as shown in fig. 10 for the user to select, and if the user selects dopamine therein, the display interface on the right side as shown in fig. 10 is entered, which means that the infusion protocol corresponding to the previously configured "dopamine" is used as the target infusion protocol.

After selecting the target infusion protocol, the healthcare worker may directly apply the target infusion protocol, that is, the target infusion protocol may be applied directly, skipping the editing or setting steps, as a default infusion protocol, through the initial setting steps described above.

It should be noted that parameter values of some infusion parameters in the target infusion protocol are indicative, for example, drug concentration is determined based on actual concentration in the infusion pump and may be changed without editing on the infusion pump, and for some parameters such as infusion rate, the infusion process may be changed by editing on the infusion pump.

In some embodiments, the healthcare worker may also edit rapidly some of the rapidly editing parameters, which may also be defined in advance, as shown in fig. 10, the human-computer interaction device 110 may output an infusion interface 40 corresponding to the infusion protocol, the infusion interface 40 including at least one of the plurality of rapidly editing parameters predefined in the infusion parameters, and the healthcare worker may edit the rapidly editing parameters of the infusion interface 40. For example, the healthcare worker may enter the corresponding infusion interface 40 by clicking on the infusion protocol identifier 2 corresponding to the target infusion protocol to edit the fast editing parameter, where the editing includes changing the parameter value of the fast editing parameter as shown in fig. 11, or may increase the parameter value of the fast editing parameter, and the increased parameter value is also selectable by the healthcare worker during use, for example, in fig. 12, after the healthcare worker selects the target infusion protocol, the target parameter value to be applied may be determined from the two parameter values. In addition, when the quick editing parameter has at least two parameter values, the parameter values can be deleted.

The infusion interface 40 is advantageously configured to allow the healthcare worker to quickly edit or select certain commonly used parameters throughout the infusion protocol selection process to simplify the medical worker's operational flow.

During use by the medical personnel, the infusion pump also supports editing the correspondence between the first target identifier and the infusion protocol. In some embodiments, the infusion protocol corresponding to the first target identifier may be increased or decreased, for example, by deleting "dopamine" from the cardiology, and the infusion protocol corresponding to the first target identifier may be increased, for example, by adding a cardiology alternative infusion protocol from a plurality of stored infusion protocols, corresponding to an expanded cardiology alternative drug library.

In other embodiments, the healthcare worker may also call up the management interface 10 shown in fig. 6 and edit different configuration management items through the management interface 10, so as to update the infusion parameters, the alarm parameters, the consumable parameters, and the like in the memory 120. That is, after determining the first target identifier, the medical staff may determine a target configuration management item from at least one configuration management item corresponding to the first target identifier, and then edit the target configuration management item, so as to edit various types of parameters directly on the infusion pump.

In some embodiments, the infusion pump may also "intelligently" record some data, for example, the infusion pump may record the infusion protocol used by the user, advance the display position of a particular infusion protocol in the ranking sequence when the number of times the user uses a particular infusion protocol satisfies a preset condition, i.e., advance the display position of a particular infusion protocol in fig. 10, and may automatically record the parameter values of the infusion parameters for the same patient, and may quickly select the parameter values of the corresponding infusion parameters according to the patient when the patient performs the infusion again.

In some embodiments, when the classification identifier is not the department identifier stored in the memory 120, the medical staff needs to determine a third target identifier from the at least one classification identifier when using the infusion protocol, obtain at least one infusion protocol corresponding to the third target identifier according to the third target identifier and the correspondence between the classification identifier and the infusion protocol, and then determine a target infusion protocol from the at least one infusion protocol for use. That is, the medical staff determines which category the medical staff belongs to currently, and then selects the infusion scheme in the scenario.

Referring to fig. 13, fig. 13 provides a method for configuring an infusion protocol, including the steps of:

step a100, a plurality of department identifiers 1 stored in advance are output. Each department identifier 1 corresponds to a department.

In some embodiments, after the infusion pump is turned on, a display interface such as that shown in fig. 2 pops up, thereby outputting a plurality of department identifiers 1.

Step A200, when detecting that the first operation instruction is triggered, determining a first target identifier from a plurality of department identifiers 1 according to the first operation instruction.

In some embodiments, the user may determine the first target identifier by clicking the display screen to select the first target identifier to trigger the first operation instruction. In other embodiments, as shown in fig. 3, the infusion pump may further support user customization of the first target identifier, i.e. entering the first target identifier may also trigger the first operation instruction, by which the stored department identifier 1 may be increased, thereby increasing the user's subsequent selection of departments.

Step A300, a plurality of infusion scheme identifications 2 stored in advance are output, wherein each infusion scheme identification 2 corresponds to one infusion medicine.

Step a400, when it is detected that the second operation instruction is triggered, determining a second target identifier from the plurality of infusion protocol identifiers 2 according to the second operation instruction.

The triggering manner of the second operation instruction may be various, in some embodiments, the display screen of the infusion pump may pop up a display interface as shown in fig. 4, where the infusion protocol identifier 2 is presented by a name of a chinese language of the infusion drug, in other embodiments, the infusion protocol identifier 2 may also be another type of manner that can be understood by the medical staff, for example, the infusion protocol identifier 2 is a latin abbreviation of the infusion drug, and the user may select the second target identifier by clicking the display screen to trigger the second operation instruction, so as to determine the second target identifier, and in fig. 4, a classification label 3 corresponding to the infusion protocol identifier 2 is further provided to help the user to quickly find the corresponding second target identifier, and since the infusion protocol identifier 2 is presented by a name of the infusion drug in fig. 4, the classification label 3 is set based on the type of the infusion drug, and the user may quickly check the infusion drug of the department, the vasoactive type, the sedation type, and analgesia type on the display interface. In other embodiments, the infusion pump may further support user-defined second target identifier, that is, inputting the second target identifier may also trigger the second operation instruction, and the input manner includes, but is not limited to, text input, voice input, and input via an external device, for example, the infusion drug may be entered by scanning a bar code of a drug package through a connected bar code, or by photographing the drug package and then recognizing the infusion drug through a pre-stored recognition algorithm, so as to enter the infusion drug, which may increase the database of the infusion protocol identifier 2, and when the user wants to configure an infusion protocol corresponding to another department next time, there may be more choices from the database of the infusion protocol identifier 2.

Step A500, associating the first target identifier with the second target identifier to obtain an association relationship between the first target identifier and the second target identifier.

In the case that the second target identifier corresponds to the infused drug, the association relationship between the department and the infused drug is actually bound.

Step A600, outputting a plurality of pre-stored infusion parameters of parameter values to be set.

Step A700, obtaining the settings of the user on the parameter values of the plurality of infusion parameters, and forming an infusion scheme associated with the second target identifier.

It should be noted that the term "parameter value" in this application does not only include parameter values in numerical categories, but also includes other types of parameter values, such as displayed text, colors, and various information.

Step A800, obtaining and storing the corresponding relation between the first target identification and the infusion scheme according to the incidence relation between the first target identification and the second target identification.

Since the association relationship between the first target identifier and the second target identifier is obtained in the above steps, after the configuration of the infusion scheme corresponding to the second target identifier is completed, that is, the infusion scheme is the infusion scheme used in the department corresponding to the first target identifier, the correspondence relationship between the first target identifier and the infusion scheme can be obtained, and then the correspondence relationship between the first target identifier and the infusion scheme is stored. The above process is a process of configuring an infusion scheme for a department, the infusion scheme is saved after the save button is clicked in fig. 5, if the return button at the upper left corner in fig. 5 is clicked, the process returns to the display interface shown in fig. 4, a second target identifier associated with the first target identifier may be further added to the display interface, so that the infusion scheme associated with the department corresponding to the first target identifier is added. After the infusion schemes related to a certain department are configured, the user can return to the display interface shown in fig. 2 to select and configure the infusion scheme required by the next department corresponding to the first target identifier. Through repeated operations, the memory 120 may store a correspondence relationship between a plurality of department identifiers 1 and a plurality of infusion protocols, where each department identifier 1 corresponds to at least one infusion protocol, and infusion protocols corresponding to different department identifiers 1 may be the same or different, for example, both department a and department B have dopamine-related infusion protocols, and infusion parameters of the two infusion protocols may be identical. The correspondence between department identity 1 and infusion protocol may be stored in the form of a mapping table.

In some embodiments, the correspondence between the department identifier 1 and at least one type of configuration management item may be further stored in advance, and the management interface 10 corresponding to the first target identifier may be further output in response to an operation of the user, where the management interface 10 includes at least one category guidance control 4, each category guidance control 4 is used to guide the user to complete editing of one type of configuration management item, and one of the configuration management items is an infusion scheme, that is, the infusion scheme may be edited through the management interface 10. For example, when the user selects department identifier 1 corresponding to "department of cardiology" in fig. 2, the human-computer interaction device 110 may output the management interface 10 in fig. 6, wherein three classification guidance controls 4 are disposed on the management interface 10, wherein: the infusion protocol display system comprises a classification guiding control 4 of 'drug management', wherein the classification guiding control 4 is used for guiding a user to complete the editing of an infusion protocol, when the user clicks 'drug management', the management interface 10 is switched to a first editing interface 20, the first editing interface 20 is similar to the interface shown in fig. 4, the infusion protocol identifier 2 is displayed in the mode of infusing the drug name, and the user can trigger a second operation instruction to determine a second target identifier through selection operation in the first editing interface 20. In the interface shown in fig. 6, it is indicated that the user clicks and selects the infusion scheme identifier 2 of "dopamine" as the second target identifier, then the first editing interface 20 is switched to the second editing interface 30 corresponding to "dopamine", the user can complete editing of the parameter values of the corresponding infusion parameters in the second editing interface 30, the meaning of the contents included in the second editing interface 30 is similar to that in fig. 5, which is not described herein again, and when the user completes editing of the parameter values of the infusion parameters in the second editing interface 30, the configuration of the infusion scheme corresponding to "dopamine" is also completed, and the infusion scheme can be stored; the system also comprises a classification guiding control 4 of 'configuration management', wherein the classification guiding control 4 is used for guiding a user to complete the setting of a configuration management item of alarm parameters, as shown in fig. 7, after the user clicks 'configuration management', a management interface 10 is switched to an alarm editing interface, and the user can complete the editing of the alarm parameters on the alarm editing interface, for example, as shown in fig. 7 and 8, the alarm parameters can be various alarm limit parameters, common alarm limit parameters include but are not limited to blocking pressure, approaching completion time, approaching completion allowance, bubble size, speed soft/hard upper limit, and speed soft/hard lower limit, wherein the speed soft upper limit refers to an upper infusion speed limit which needs to be noticed but can be accepted, the speed hard upper limit refers to an upper infusion speed limit which needs to be noticed but can be accepted, and similarly, the speed soft lower limit refers to a lower infusion speed limit which needs to be noticed but can be accepted, and the speed hard lower limit refers to an infusion speed lower limit which is strictly forbidden; still guide control 4 including this classification of "brand management", this classification guides control 4 to be used for guiding the user to accomplish the edition of this configuration management item of consumptive material parameter, as shown in fig. 9, after the user clicks "brand management", management interface 10 can switch over to consumptive material editing interface, the consumptive material brand that shows in this consumptive material editing interface in the consumptive material brand storehouse supplies the user to select, consumptive material class parameter is used for the brand that the sign infusion medicine adopted, can prestore the brand that obtains through the investigation consumptive material storehouse supplies the user to select.

Referring to fig. 14, in an embodiment shown in fig. 14, an infusion control method of an infusion pump is provided, including the steps of:

and step B100, outputting at least one preset department mark 1. Each department identifier 1 corresponds to a department.

And step B200, when the triggering of the first selection instruction is detected, determining a first target identifier from at least one department identifier 1 according to the first selection instruction.

In some embodiments, after the infusion pump is turned on, the medical staff may enter a display interface for department selection, a department identifier 1 corresponding to a department for which an infusion scheme has been configured is displayed in the display interface for department selection, and the medical staff may select the first target identifier according to a need of the medical staff, for example, the display interface shown in fig. 1 is displayed.

And step B300, outputting at least one infusion scheme corresponding to the first target identification according to the preset corresponding relation between the department identification and the infusion scheme. Wherein the infusion protocol comprises a preset default infusion protocol, and each infusion protocol corresponds to one infusion drug. How the default infusion protocol is obtained can be referred to the description in steps a100 to a800, and the medical staff can apply the default infusion protocol directly without modification.

Step B400, when the second selection instruction is detected to be triggered, determining a target infusion scheme from at least one infusion scheme corresponding to the first target identification according to the second selection instruction.

In some embodiments, when the user selects the department of cardiology, the display screen of the infusion pump may display a left display interface as shown in fig. 10 for the user to select, and if the user selects dopamine therein, the display interface on the right side as shown in fig. 10 is entered, which means that the infusion protocol corresponding to the previously configured "dopamine" is used as the target infusion protocol.

After selecting the target infusion protocol, the medical personnel may directly apply the target infusion protocol, in which case the target infusion protocol is actually the default infusion protocol. It should be noted that parameter values of some infusion parameters in the target infusion protocol are indicative, e.g., drug concentration is determined based on actual concentration in the infusion pump and may be changed without editing on the infusion pump, and for some parameters such as infusion rate, the infusion process may be changed by editing on the infusion pump.

In some embodiments, the healthcare worker may also edit rapidly some of the rapidly editable parameters, which may also be defined in advance, as shown in fig. 10, and may output an infusion interface 40 corresponding to the infusion protocol in response to the user's operation, where the infusion interface 40 includes at least one of the rapidly editable parameters predefined in the plurality of infusion parameters, and the healthcare worker may edit the rapidly editable parameters of the infusion interface 40. For example, the healthcare worker may enter the corresponding infusion interface 40 by clicking on the infusion protocol identifier 2 corresponding to the target infusion protocol to edit the fast editing parameter, where the editing includes changing the parameter value of the fast editing parameter as shown in fig. 11, or may increase the parameter value of the fast editing parameter, and the increased parameter value is also selectable by the healthcare worker during use, for example, in fig. 12, after the healthcare worker selects the target infusion protocol, the target parameter value to be applied may be determined from the two parameter values. In addition, when the quick editing parameter has at least two parameter values, the parameter values can be deleted.

In other embodiments, the healthcare worker may also call the management interface 10 shown in fig. 6, and edit different configuration management items through the management interface 10, so as to update the stored infusion parameters, alarm parameters, consumable parameters, and the like. That is, after determining the first target identifier, the medical staff may determine a target configuration management item from at least one configuration management item corresponding to the first target identifier, and then edit the target configuration management item, so as to edit various types of parameters directly on the infusion pump.

In some embodiments, the infusion pump may also "intelligently" record some data, for example, the infusion pump may record the infusion protocol used by the user, advance the display position of the specific infusion protocol in the ranking sequence when the number of times the user uses the specific infusion protocol satisfies a preset condition, i.e., advance the display position of the specific infusion protocol in fig. 10, and may automatically record the parameter values of the infusion parameters for the same patient, and when the patient performs the infusion again, the parameter values of the corresponding infusion parameters may be quickly selected according to the patient.

The infusion pump of the embodiment can be initially set to number the infusion schemes, so that medical personnel can quickly find the appropriate infusion scheme by selecting specific classifications of departments and the like, and can perform subsequent maintenance and editing on the infusion pump.

Those skilled in the art will appreciate that all or part of the functions of the various methods in the above embodiments may be implemented by hardware, or may be implemented by computer programs. When all or part of the functions of the above embodiments are implemented by a computer program, the program may be stored in a computer-readable storage medium, and the storage medium may include: a read only memory, a random access memory, a magnetic disk, an optical disk, a hard disk, etc., and the program is executed by a computer to realize the above functions. For example, the program may be stored in a memory of the device, and when the program in the memory is executed by the processor, all or part of the functions described above can be implemented. In addition, when all or part of the functions in the above embodiments are implemented by a computer program, the program may be stored in a storage medium such as a server, another computer, a magnetic disk, an optical disk, a flash disk, or a portable hard disk, and may be downloaded or copied to a memory of a local device, or may be version-updated in a system of the local device, and when the program in the memory is executed by a processor, all or part of the functions in the above embodiments may be implemented.

The present invention has been described in terms of specific examples, which are provided to aid in understanding the invention and are not intended to be limiting. For a person skilled in the art to which the invention pertains, several simple deductions, modifications or substitutions may be made according to the idea of the invention.

Claims

1. An infusion pump, comprising:

the department identification management system comprises a memory, a database and a management server, wherein the memory is used for storing a plurality of infusion schemes, at least one department identification and a corresponding relation between the department identification and the infusion schemes; wherein the infusion protocol comprises a preset default infusion protocol, each infusion protocol corresponds to one infusion drug, and each department identifier corresponds to one department;

2. The infusion pump of claim 1, wherein the processor is further configured to: and when a first editing instruction is detected, editing the corresponding relation between the first target identification and the infusion scheme according to the first editing instruction.

3. The infusion pump of claim 2, wherein said editing a correspondence between the first target identification and an infusion protocol according to the first editing instruction comprises: and controlling the human-computer interaction device to output at least one of a plurality of infusion schemes stored in the memory, and establishing a corresponding relation between the first target identifier and at least one of the plurality of infusion schemes according to the first editing instruction.

4. The infusion pump of claim 1, wherein the infusion protocol includes a plurality of infusion parameters associated with an infusion process, each of the infusion parameters having a preset parameter value.

5. The infusion pump of claim 4, wherein the human interaction device is further configured to:

outputting an infusion interface corresponding to the infusion protocol, the infusion interface including at least one fast editing parameter predefined among the plurality of infusion parameters;

the processor is further configured to:

and when a second editing instruction is detected, editing the at least one fast editing parameter.

6. The infusion pump of claim 5, wherein at least one of the quick-edit parameters has at least two parameter values, the processor further configured to: and controlling the human-computer interaction device to output at least two parameter values of the quick editing parameter, and determining a target parameter value from the at least two parameter values of the quick editing parameter according to a third selection instruction when the third selection instruction is triggered.

7. The infusion pump of claim 2,

the memory is also used for storing the corresponding relation between the department identification and at least one type of configuration management item;

the human-computer interaction device is also used for:

outputting a management interface corresponding to the first target identifier, wherein the management interface comprises at least one classification guidance control, each classification guidance control is used for guiding a user to complete the editing of one type of the configuration management items, and one type of the configuration management items in at least one type comprises the plurality of infusion schemes; and

and responding to the input of the user to the classification guide control, and outputting an editing interface of the configuration management item corresponding to the classification guide control, wherein the editing interface is used for receiving the editing of the user to the configuration management item.

8. The infusion pump of claim 7, wherein the editing interfaces of any of the infusion protocols comprise a first editing interface and a second editing interface, wherein the first editing interface comprises at least one infusion protocol identifier therein, each infusion protocol identifier corresponds to one infusion drug, each infusion protocol identifier is linked to the corresponding second editing interface, and the second editing interface comprises a plurality of parameter setting items corresponding to the infusion protocols;

the human-computer interaction device is also used for:

outputting a first editing interface; and

responding to a second target identification determined by a user from at least one infusion scheme identification in the first editing interface, and outputting a second editing interface corresponding to the second target identification;

the processor is further configured to:

and receiving the first editing instruction of the user aiming at the parameter setting item, and changing the corresponding infusion scheme stored in the memory.

9. The infusion pump of claim 7 or 8, wherein the configuration management further comprises alarm parameters for characterizing parameters that act as limitations during an infusion process and consumable type parameters for characterizing a brand used for the infusion of the drug.

10. The infusion pump as claimed in claim 1, wherein said first selection command triggering mode comprises: the processor responds to the selection operation of any department identifier input by a user through the human-computer interaction device to trigger the first selection instruction; or the memory further stores matching relation between medical information and departments, the processor further acquires medical information associated with the departments, and triggers the first selection instruction according to the medical information and the matching relation between the medical information and the departments, wherein the medical information comprises at least one of first identity information of a user, second identity information of an infusion object of the infusion pump, medical order information and position information of the infusion pump.

11. The infusion pump of claim 1, wherein when the infusion protocol corresponding to the first target identifier includes at least two, the processor controls the human-computer interaction device to output at least one of the infusion protocols, including: the processor controls a display interface of the human-computer interaction device to display the at least two infusion schemes at different display positions in a preset arrangement sequence.

12. The infusion pump of claim 11, wherein the processor is further configured to: recording an infusion protocol used by a user, and advancing a display position of a specific infusion protocol in the arrangement sequence when a number of times the user uses the specific infusion protocol satisfies a preset condition.

13. An infusion pump, comprising:

a memory for storing a plurality of infusion protocols, at least one class identifier, and a correspondence of the class identifier to an infusion protocol; wherein the infusion protocol comprises a preset default infusion protocol, the at least one classification identifying a particular classification used to characterize the infusion protocol;

14. An infusion pump, comprising:

15. An infusion pump, comprising:

the infusion device comprises a memory, a first infusion module, a second infusion module and a control module, wherein the memory is used for storing a plurality of department identifications, a plurality of infusion scheme identifications and a plurality of infusion parameters of parameter values to be set, each department identification corresponds to one department, and each infusion scheme identification corresponds to one infusion medicine;

16. The infusion pump as claimed in claim 15, wherein said triggering of said first operating command comprises: the processor responds to the selection operation of any department identifier input by a user through the human-computer interaction device, and triggers the first operation instruction; or the processor responds to a department identifier input through the man-machine interaction device from the outside to trigger the first operation instruction.

17. The infusion pump according to claim 15 or 16, wherein the triggering mode of the second operating instruction comprises: the processor responds to the selected operation of any infusion scheme identifier input by the user through the human-computer interaction device, and triggers the second operation instruction; or the processor responds to an infusion scheme identifier input externally through the man-machine interaction device and triggers the second operation instruction.

18. The infusion pump of claim 15, wherein said memory is further configured to store a correspondence between said department identifier and at least one type of configuration management item;

the human-computer interaction device is also used for:

outputting a management interface corresponding to the first target identifier, wherein the management interface comprises at least one classification guidance control, each classification guidance control is used for guiding a user to complete the editing of one type of the configuration management item, and one type of the configuration management item in at least one type comprises the infusion scheme; and

19. The infusion pump of claim 18, wherein the editing interfaces of any of the infusion protocols comprise a first editing interface and a second editing interface, wherein the first editing interface comprises at least one infusion protocol identifier therein, each infusion protocol identifier corresponds to one infusion drug, each infusion protocol identifier is linked to the corresponding second editing interface, and the second editing interface comprises a plurality of parameter setting items corresponding to the infusion protocols;

the human-computer interaction device is also used for:

outputting a first editing interface; and

responding to a second target identification determined by the user from at least one infusion scheme identification in the first editing interface, and outputting a second editing interface corresponding to the second target identification;

the processor is further configured to:

and receiving the setting of the user for the parameter setting item to obtain the parameter value of at least one infusion parameter.

20. The infusion pump of claim 18 or 19, wherein the configuration management items include alarm parameters for characterizing parameters that act as limitations during an infusion process and consumable type parameters for characterizing a brand used for the infusion of a drug.

21. An infusion pump, comprising:

a memory for storing at least one classification identifier, a plurality of infusion protocol identifiers, and a plurality of infusion parameters for which parameter values are to be set, the at least one classification identifier each being used to characterize a particular classification of the infusion protocol;

22. An infusion control method of an infusion pump, comprising:

23. The method of claim 22, wherein the method further comprises: when a first editing instruction is detected, editing the corresponding relation between the first target identification and the infusion scheme according to the first editing instruction.

24. The method of claim 23, wherein said compiling a correspondence between the first target identification and an infusion protocol in accordance with the first compilation instruction comprises: and outputting at least one of a plurality of prestored infusion schemes, and establishing a corresponding relation between the first target identifier and at least one of the plurality of infusion schemes according to the first editing instruction.

25. The method of claim 22, wherein the infusion protocol includes a plurality of infusion parameters associated with an infusion process, each of the infusion parameters having a preset parameter value.

26. The method of claim 25, wherein the method further comprises: outputting an infusion interface corresponding to the infusion protocol, the infusion interface including at least one predefined quick edit parameter of the plurality of infusion parameters, the at least one quick edit parameter being edited when a second edit instruction is detected.

27. The method of claim 26, wherein at least one of said fast edit parameters has at least two parameter values, said method further comprising: and outputting at least two parameter values of the fast editing parameter, and determining a target parameter value from the at least two parameter values of the fast editing parameter according to a third selection instruction when the third selection instruction is triggered.

28. The method of claim 24, wherein the method further comprises:

outputting a management interface corresponding to the first target identifier, wherein the management interface comprises at least one classification guide control, each classification guide control is used for guiding a user to complete the editing of one type of configuration management item, and the department identifier and the at least one type of configuration management item have a preset corresponding relationship; one of the configuration management items of at least one type includes the plurality of infusion protocols;

29. The method of claim 28, wherein the editing interfaces of any of the infusion protocols comprise a first editing interface and a second editing interface, wherein the first editing interface comprises at least one infusion protocol identifier therein, wherein each infusion protocol identifier corresponds to one infusion drug, wherein each infusion protocol identifier is linked to a corresponding second editing interface, wherein the second editing interface comprises a plurality of parameter setting items corresponding to the infusion protocols, and wherein the method further comprises: outputting a first editing interface; and responding to a second target identifier determined by the user from at least one infusion scheme identifier in the first editing interface, outputting a second editing interface corresponding to the second target identifier, receiving the first editing instruction of the user for the parameter setting item, and changing a corresponding infusion scheme stored in advance.

30. The method of claim 28 or 29, wherein the configuration management items further comprise alarm parameters for characterizing parameters that play a limiting role in the infusion process and consumable type parameters for characterizing the brand used for infusing the drug.

31. A method of configuring an infusion protocol, comprising:

outputting a plurality of department identifications stored in advance, and when a first operation instruction is triggered, determining a first target identification from the plurality of department identifications according to the first operation instruction, wherein each department identification corresponds to a department;

32. The method of claim 31, wherein the manner in which the first operation instruction is triggered comprises: responding to the selection operation of a user on any department identifier, and triggering the first operation instruction; or responding to a department identification input from the outside to trigger the first operation instruction.

33. The method of claim 31 or 32, wherein the triggering of the second operation instruction comprises: responding to the selected operation of the user on any infusion scheme identifier, and triggering the second operation instruction; or the second operation instruction is triggered in response to the infusion scheme identification input from the outside.

34. The method of claim 31, wherein the method further comprises:

outputting a management interface corresponding to the first target identifier, wherein the management interface comprises at least one classification guide control, each classification guide control is used for guiding a user to complete editing of one type of configuration management item, the department identifier and at least one type of configuration management item have a preset corresponding relation, and one type of configuration management item in the at least one type comprises the infusion scheme; and

35. The method of claim 34, wherein the editing interfaces of any of the infusion protocols comprise a first editing interface and a second editing interface, wherein the first editing interface comprises at least one infusion protocol identifier therein, wherein each infusion protocol identifier corresponds to one infusion drug, wherein each infusion protocol identifier is linked to a corresponding second editing interface, wherein the second editing interface comprises a plurality of parameter settings corresponding to the infusion protocols, and wherein the method further comprises:

outputting a first editing interface; and

36. The method of claim 34 or 35, wherein the configuration management items include alarm parameters for characterizing parameters that play a limiting role in the infusion process and consumable type parameters for characterizing the brand used for infusing the drug.

37. A computer-readable storage medium, characterized in that the medium has stored thereon a program which is executable by a processor to implement the method of any one of claims 22 to 36.