WO2024040394A1 - Drug infusion device and drug infusion system - Google Patents

Drug infusion device and drug infusion system Download PDF

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Publication number
WO2024040394A1
WO2024040394A1 PCT/CN2022/113979 CN2022113979W WO2024040394A1 WO 2024040394 A1 WO2024040394 A1 WO 2024040394A1 CN 2022113979 W CN2022113979 W CN 2022113979W WO 2024040394 A1 WO2024040394 A1 WO 2024040394A1
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WO
WIPO (PCT)
Prior art keywords
infusion
information
drug infusion
processor
drug
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PCT/CN2022/113979
Other languages
French (fr)
Chinese (zh)
Inventor
黄浩科
董俊
Original Assignee
深圳麦科田生物医疗技术股份有限公司
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Application filed by 深圳麦科田生物医疗技术股份有限公司 filed Critical 深圳麦科田生物医疗技术股份有限公司
Priority to PCT/CN2022/113979 priority Critical patent/WO2024040394A1/en
Priority to CN202280004926.0A priority patent/CN116096442A/en
Publication of WO2024040394A1 publication Critical patent/WO2024040394A1/en

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    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B5/00Measuring for diagnostic purposes; Identification of persons
    • A61B5/02Detecting, measuring or recording pulse, heart rate, blood pressure or blood flow; Combined pulse/heart-rate/blood pressure determination; Evaluating a cardiovascular condition not otherwise provided for, e.g. using combinations of techniques provided for in this group with electrocardiography or electroauscultation; Heart catheters for measuring blood pressure
    • A61B5/021Measuring pressure in heart or blood vessels
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B5/00Measuring for diagnostic purposes; Identification of persons
    • A61B5/145Measuring characteristics of blood in vivo, e.g. gas concentration, pH value; Measuring characteristics of body fluids or tissues, e.g. interstitial fluid, cerebral tissue
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B5/00Measuring for diagnostic purposes; Identification of persons
    • A61B5/24Detecting, measuring or recording bioelectric or biomagnetic signals of the body or parts thereof
    • A61B5/316Modalities, i.e. specific diagnostic methods
    • A61B5/318Heart-related electrical modalities, e.g. electrocardiography [ECG]
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61MDEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M5/00Devices for bringing media into the body in a subcutaneous, intra-vascular or intramuscular way; Accessories therefor, e.g. filling or cleaning devices, arm-rests
    • A61M5/14Infusion devices, e.g. infusing by gravity; Blood infusion; Accessories therefor
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61MDEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M5/00Devices for bringing media into the body in a subcutaneous, intra-vascular or intramuscular way; Accessories therefor, e.g. filling or cleaning devices, arm-rests
    • A61M5/14Infusion devices, e.g. infusing by gravity; Blood infusion; Accessories therefor
    • A61M5/142Pressure infusion, e.g. using pumps
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61MDEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M5/00Devices for bringing media into the body in a subcutaneous, intra-vascular or intramuscular way; Accessories therefor, e.g. filling or cleaning devices, arm-rests
    • A61M5/14Infusion devices, e.g. infusing by gravity; Blood infusion; Accessories therefor
    • A61M5/168Means for controlling media flow to the body or for metering media to the body, e.g. drip meters, counters ; Monitoring media flow to the body
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61MDEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M5/00Devices for bringing media into the body in a subcutaneous, intra-vascular or intramuscular way; Accessories therefor, e.g. filling or cleaning devices, arm-rests
    • A61M5/14Infusion devices, e.g. infusing by gravity; Blood infusion; Accessories therefor
    • A61M5/168Means for controlling media flow to the body or for metering media to the body, e.g. drip meters, counters ; Monitoring media flow to the body
    • A61M5/172Means for controlling media flow to the body or for metering media to the body, e.g. drip meters, counters ; Monitoring media flow to the body electrical or electronic

Definitions

  • This application relates to the technical field of medical devices, for example, to a drug infusion device and a drug infusion system.
  • Drug infusion equipment is increasingly used, and drug infusion equipment usually has patient-controlled analgesia (PCA) functions.
  • PCA patient-controlled analgesia
  • a certain dose of drug delivery can be completed by controlling the drug infusion device to relieve the patient's pain.
  • This application provides a drug infusion device and a drug infusion system to solve the problem that the drug infusion device cannot transmit information.
  • a drug infusion device includes: a housing, a driving device, a flow path, a data communication component, and at least one processor; the processor is respectively connected to the The driving device and the data communication component are electrically connected; the driving device, the data communication component and at least one processor are arranged in the housing;
  • the data communication component is communicatively connected with the infusion control device, and is configured to receive the infusion control information sent by the infusion control device and transmit the infusion control information to the processor;
  • the processor is configured to control the driving device to operate based on the infusion control information to output the liquid in the flow path.
  • a drug infusion system which includes: an infusion control device and the drug infusion device described in any embodiment of the present application;
  • the infusion control device includes a data collection component, wherein the data collection component is configured to collect infusion control information.
  • Figure 1 is a schematic structural diagram of a drug infusion device provided according to Embodiment 1 of the present application.
  • FIG. 2 is a schematic flow chart of data processing provided according to Embodiment 1 of the present application.
  • FIG. 3 is a schematic structural diagram of a processor execution module provided according to Embodiment 1 of the present application.
  • Figure 4 is a schematic structural diagram of a drug infusion system provided according to Embodiment 2 of the present application.
  • Figure 5 is a schematic structural diagram of a data collection component provided according to Embodiment 2 of the present application.
  • Figure 6 is a schematic structural diagram of another drug infusion system provided according to Embodiment 2 of the present application.
  • Figure 7 is a schematic structural diagram of another drug infusion system provided according to Embodiment 2 of the present application.
  • Figure 8 is a schematic structural diagram of a PCA controller provided according to Embodiment 2 of the present application.
  • Figure 9 is a schematic structural diagram of an infusion pump provided according to Embodiment 2 of the present application.
  • Figure 1 is a schematic structural diagram of a drug infusion device provided in Embodiment 1 of the present application. This embodiment can be applied to situations where the infusion control device controls the drug infusion device.
  • the drug infusion device includes: a housing 100, a driving device 110, a flow path 120, a data communication component 130, and at least one processor 140; the processor 140 is connected to the driving device 110 and the data communication component 130 respectively.
  • the driving device 110, the data communication component 130 and the at least one processor 140 are disposed in the housing 100; the data communication component 130 is communicatively connected with the infusion control device and is configured to receive the infusion control sent by the infusion control device The information transmits the infusion control information to the processor 140; the processor 140 is configured to control the driving device 110 to operate based on the infusion control information to output the liquid in the flow path 120.
  • the housing 100 refers to the shell-shaped component of the drug infusion device.
  • the driving device 110 refers to a device for driving the liquid output in the flow path 120, and the driving device 110 and the flow path 120 are connected through a liquid passage.
  • the driving device 110 may be a pump.
  • the flow path 120 refers to a pipeline with the function of storing or transmitting liquid. It can be understood that the flow path 120 in FIG. 1 is only for example, and the flow path 120 may be entirely located inside the housing 100 or partially located outside the housing 100 .
  • the data communication component 130 refers to a component that performs data transmission.
  • the communication method corresponding to the communication connection includes wired communication and wireless communication.
  • the data communication component 130 can be a wireless communication module such as Bluetooth, Wireless Fidelity (WIFI), Radio Frequency Identification (RFID), etc., or it can also be a wired communication module.
  • the processor 140 refers to an electronic device used for data processing.
  • the processor 140 can be used to perform data processing operations such as analog-to-digital conversion, serial-to-parallel conversion, and data processing on signals.
  • Infusion control information refers to control signals that can be used to control the driving device 110 .
  • the infusion control device can generate infusion control information by operating the infusion control device, and the infusion control device sends the infusion control information to the drug infusion device through wired or wireless communication, and the drug infusion
  • the processor 140 of the device can control the driving device 110 to operate according to the infusion control information to output the liquid in the flow path 120 .
  • the processor 140 is further configured to control the driving device 110 based on the physiological parameter information received by the data communication component 130 .
  • the data communication component 130 is also configured to receive physiological parameter information and transmit the physiological parameter information to the processor 140, where the processor 14 can control the driving device according to the received physiological parameter information.
  • physiological parameter information can be collected through the physiological parameter acquisition module.
  • the physiological parameter acquisition module can be set on the infusion control device, or can be distributed on other devices such as wearable devices and medical equipment.
  • the physiological parameter collection module includes a blood pressure collection module, an ECG collection module, a blood oxygen collection module, a heart rate collection module and a compression collection module.
  • the blood pressure acquisition module is configured to collect the blood pressure analog signal of the infusion subject
  • the ECG acquisition module is configured to collect the ECG analog signal of the infusion subject
  • the blood oxygen acquisition module is configured to collect the blood oxygen of the infusion subject.
  • the heart rate acquisition module is set to collect the heart rate analog signal of the infusion subject. It can be understood that by obtaining the user's physiological parameter information, real-time monitoring of physiological parameters is achieved.
  • FIG. 2 is a schematic flowchart of data processing provided according to this embodiment.
  • the data processing steps may include: S10, obtaining physiological parameter information; S20, performing data analysis on the physiological parameter information, and obtaining analysis results; S30, adjusting the infusion parameters of the drug infusion equipment according to the analysis results.
  • FIG. 3 is a schematic structural diagram of a processor execution module provided in this embodiment.
  • the processor 140 receives physiological parameter information such as heart rate, blood pressure, blood oxygen, end-tidal carbon dioxide (CO2), and ECG, it can use the data to The analysis module 141 performs data analysis on the physiological parameter information.
  • the data analysis module 141 can be a packaging module of the data analysis method.
  • the data analysis module 141 can be configured in the processor 140 .
  • the infusion parameters of the drug infusion device can be adjusted according to the analysis results, and relevant information can be sent out through the data communication component 130.
  • the relevant information can include analysis results, physiological parameters and other information.
  • the processor 140 can perform analog-to-digital conversion on the heart rate analog signal to obtain the heart rate. If the heart rate exceeds a preset heart rate threshold or the heart rate change exceeds a preset rule, the work of the driving device 110 can be suspended or Reduce the driving speed of the driving device 110 or the like.
  • the heart rate change may be a change amount within a preset time interval, a change amount between preset sampling intervals, a heart rate change rate, a change prediction amount, etc.
  • the preset rule can be: the change in the preset time interval exceeds the preset heart rate change threshold; or the preset sampling interval, such as the change in heart rate collected twice in a row or the heart rate sampled two times apart. The change amount exceeds the preset heart rate change threshold; or the heart rate change rate or the predicted amount of heart rate change exceeds the preset change threshold.
  • the data communication component 130 is further configured to send at least one of the physiological parameter information and the preprocessed physiological parameter information to the cloud server.
  • the preprocessed physiological parameter information refers to the physiological parameter information that has been preprocessed. Preprocessing operations include screening, cleaning, normalization, etc. It should be noted that at least one of the physiological parameter information uploaded to the cloud server and the preprocessed physiological parameter information can be used for big data analysis and processing.
  • the processor 140 is further configured to: judge the infusion control information based on the preset judgment rules; when the infusion control information does not comply with the preset judgment rules , determine the current control operation as an invalid operation, and generate an alarm signal.
  • the preset judgment rule refers to a preset control signal judgment rule.
  • the preset judgment rule can be a threshold judgment rule.
  • the frequency of the received infusion control information is A
  • the preset judgment rule is A.
  • the frequency range corresponding to the judgment rule is B-C. If A is not within the B-C frequency range, the current control operation is determined to be an invalid operation. Invalid operations refer to operations that have not taken effect.
  • the infusion control information may include pressing information, handwriting input information, gesture information, etc.
  • the infusion control information includes at least one of the compression frequency, the number of compressions, and the compression duration; accordingly, the preset judgment rule can be a compression judgment rule, and the invalid operation can be invalid compression.
  • the drug infusion device may generate infusion parameter adjustment information based on at least one of the compression frequency, the number of compressions, and the compression duration to control the driving device 110 based on the infusion parameter adjustment information.
  • the infusion parameter adjustment information can have a corresponding relationship with the compression frequency, the number of compressions, and the compression duration.
  • the infusion parameter adjustment information can be the dosage of medication.
  • One press corresponds to an increase in dose A, and two presses correspond to an increase in dose B. dose.
  • Infusion parameters refer to the working parameters of the infusion pump, which can include drug dosage, infusion speed, etc.
  • control button is pressed once, the corresponding dose will be increased or decreased; or, if the control button is pressed for a long time (for example, for more than 5 seconds), a control signal such as pause or start will be generated to control the infusion pump to stop. run.
  • the technical solution of the embodiment of the present application realizes information transmission between the infusion control device and the drug infusion device through the data communication component of the drug infusion device, solving the problem that the drug infusion device cannot transmit information, thereby achieving Control of drug infusion equipment.
  • Figure 4 is a schematic structural diagram of a drug infusion system provided in Embodiment 2 of the present application.
  • the drug infusion system includes: an infusion control device 200 and the drug infusion device described in any embodiment of the present application; the infusion control device 200 includes a data acquisition component 210, wherein the data acquisition component 210 is Set to collect infusion control information.
  • the data collection component 210 can be disposed on the device body, or can be disposed on other devices in a distributed manner.
  • the data collection component 210 is also configured to collect the user's physiological parameter information.
  • FIG. 5 is a schematic structural diagram of a data collection component provided in this embodiment.
  • the data collection component 210 may include a control signal collection module 211 and a physiological parameter collection module 212.
  • the control signal acquisition module 211 is configured to collect infusion control information
  • the control signal acquisition module 211 can be in the form of a button or a key.
  • the physiological parameter collection module 212 is configured to collect the user's physiological parameter information.
  • Figure 6 is a schematic structural diagram of another drug infusion system provided by this embodiment.
  • the infusion control device 200 also includes: an identity recognition module 220, which is configured to collect the user's identity verification information, Authentication information is used to verify the user's identity.
  • the identity recognition module 220 refers to a module that performs identity verification.
  • the verification methods of the identity recognition module 220 may include password verification, control gesture verification, fingerprint verification, facial information verification, wireless bracelet verification, etc. It is understandable that the wireless bracelet can be equipped with near field communication function modules such as Near Field Communication (NFC), and identity authentication can be achieved through NFC and other near field communication function modules.
  • NFC Near Field Communication
  • the identity recognition module 220 is configured to collect the user's identity verification information, and send the identity verification information to the data collection component 210 or the data processor 230 of the infusion control device 200; accordingly, the data processor 230 Or the data collection component 210 is also configured to receive the identity verification information sent by the identity recognition module 220, and match the identity verification information with the reserved verification information. If the identity verification information matches successfully, the identity verification is successful, indicating that the current infusion control device The operator of 200 has the right to operate; if the identity verification information does not match successfully, the identity verification fails, indicating that the operator of the current infusion control device 200 does not have the right to operate.
  • the identity recognition module 220 is configured to collect the user's identity verification information and transmit the identity verification information to the drug infusion device; accordingly, the drug infusion device receives the identity verification information and compares the identity verification information with the predetermined Verification information is left for matching. If the identity verification information matches successfully, the identity verification is successful, indicating that the operator of the current infusion control device 200 has the authority to operate, and the successful verification result is returned to the infusion control device 200; if the identity verification information does not match If successful, the identity verification fails, indicating that the current operator of the infusion control device 200 does not have the right to operate.
  • the data processor 230 or the data collection component 210 determines that the identity verification is successful only after receiving a successful verification result returned by the drug infusion device.
  • control button can be integrated with a fingerprint module, that is, the user can complete user identity verification while pressing the control button, which can be used to confirm whether the operating user is himself or an authorized person.
  • the identity recognition module 220 may be an RFID module.
  • the RFID module identifies the user's badge or bracelet to obtain the user's identity.
  • the user's identity may include medical workers, patients, etc.
  • the data processor 230 of the infusion control device 200 is configured to: if it is determined that the identity verification of the current operator is successful based on the identity verification information, receive the drug infusion device control sent by the data acquisition component 210 signal, and determine the infusion control information based on the drug infusion equipment control signal; alternatively, the data collection component 210 is set to: if it is determined that the identity verification of the current operator is successful based on the identity verification information, collect the drug infusion equipment input by the user. control signal, and sends the drug infusion device control signal to the data processor 230 .
  • either the data collection component 210 or the data processor 230 can be used to verify the identity of the current operator.
  • patients, patients' family members, doctors, etc. may all control the infusion control device 200.
  • this embodiment divides the operating authority of different operators and enjoys different rights. Personnel with operating authority can control at least some of the parameters of the drug infusion equipment.
  • the type of operator can be determined based on the identity verification information. For example, when the type of operator is a doctor, the corresponding operating authority of the doctor is determined, and the infusion control device function corresponding to the operating authority is activated. , so that doctors can adjust the drug infusion equipment.
  • the doctor has the highest operating authority and can perform all control operations on the drug infusion equipment; the patient has the second highest authority and can control the infusion speed, start and stop of the drug infusion equipment; the patient's family has the lowest authority and can only suspend drug infusion. Note equipment.
  • the operating permissions of different operators can be divided according to actual needs.
  • different authentication methods can also be provided for different operators.
  • fingerprint verification can be used for patients
  • password verification can be used for doctors, etc.
  • the identity verification method can be set according to actual needs.
  • the above-mentioned steps of determining the operating authority of the current operator based on the identity verification information and activating the infusion control device function corresponding to the operating authority can also be performed by the data collection component 210. That is, based on the above embodiments, the data collection component 210 can also be configured to: determine the operating authority of the current operator based on the identity verification information, and activate the infusion pump control device function corresponding to the operating authority. For example, the data collection component 210 only sends the control signal of the drug infusion device to the data processor if it determines that the drug infusion device control signal input by the current operator complies with its operating authority. At this time, the data processor 230 only needs to determine the infusion control information based on the drug infusion equipment control signal sent by the data acquisition component 210.
  • FIG. 7 is a schematic structural diagram of another drug infusion system provided by this embodiment.
  • the infusion control device 200 also includes an information output component 240.
  • the information output component 240 includes a display screen. , at least one of the indicator light and the speaker.
  • the display screen is set to display at least one of the current infusion parameters and alarm information content; the prompt light is set to switch to a light state or the alarm light color in response to the alarm signal; the speaker is set to Current infusion parameters are output, and/or, in response to the alarm signal, alarm audio is output.
  • the information output component 240 may also include a vibration component, which is configured to generate vibration to feedback the user's operation.
  • the vibration component may be a motor or the like.
  • the drug infusion device may also include at least one of an identity recognition module and an information output component, the implementation of which is similar or identical to the identity recognition module and the information output component in the infusion control device 200 .
  • the infusion control device 200 when operating the infusion control device 200, the infusion control device 200 can provide feedback in the form of sound, light, vibration, etc. through the information output component, and the drug infusion device can also display relevant operation feedback information.
  • FIG. 8 is a schematic structural diagram of a PCA controller provided by an embodiment of the present application.
  • PCA Patient controlled analgesia
  • controller i.e. infusion control device
  • physiological parameter collection module 1 bracelet 2 (can be used to collect physiological parameter information), connecting cable 3, battery 4, PCA key 5 (i.e. control button), Fingerprint recognition module 6 (i.e. identity recognition module), display screen 7, prompt component 8, prompt component 8 may include an alarm (prompt) light and a speaker, etc.
  • the infusion control device can centrally collect the user's physiological parameter information and verify the user's identity through the fingerprint recognition module, thereby reducing the risk of accidental touch of the PCA controller.
  • FIG. 9 is a schematic structural diagram of an infusion pump provided by an embodiment of the present application.
  • the infusion pump i.e., drug infusion equipment
  • the infusion pump includes a switch (ON/OFF), a dose control button (Dose), a driving device, a data communication component, and at least one processor.
  • the infusion pump can communicate with a variety of medical equipment through data communication components to achieve centralized collection of physiological parameter information and avoid data loss.
  • the infusion pump can preprocess physiological parameter information and upload the preprocessed physiological parameter information to the cloud server to complete big data analysis and processing.
  • the technical solution of the embodiment of the present application realizes information transmission between the infusion control device and the drug infusion device through the data communication component of the drug infusion device, solving the problem that the drug infusion device cannot transmit data, thereby achieving Control of drug infusion equipment.

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Abstract

Disclosed in the application are a drug infusion device and a drug infusion system. The drug infusion device comprises a housing, a driving apparatus, a flow path, a data communication component, and at least one processor. The processor is separately and electrically connected to the driving apparatus and the data communication component. The driving apparatus, the data communication component and the at least one processor are arranged in the housing. The data communication component is in communication connection with an infusion control device, and is configured to receive infusion control information sent by the infusion control device and transmit the infusion control information to the processor. The processor is configured to control the driving apparatus to work on the basis of the infusion control information so as to output a liquid in the flow path.

Description

药物输注设备及药物输注系统Drug infusion equipment and drug infusion systems 技术领域Technical field
本申请涉及医疗器械技术领域,例如涉及一种药物输注设备及药物输注系统。This application relates to the technical field of medical devices, for example, to a drug infusion device and a drug infusion system.
背景技术Background technique
药物输注设备的使用越来越广泛,药物输注设备通常带有病人自控镇痛(Patient controlled analgesia,PCA)功能。当病人意识到疼痛时,可以通过控制药物输注设备完成一定剂量的药物输送,从而缓解病人的疼痛。Drug infusion equipment is increasingly used, and drug infusion equipment usually has patient-controlled analgesia (PCA) functions. When the patient is aware of pain, a certain dose of drug delivery can be completed by controlling the drug infusion device to relieve the patient's pain.
相关技术在研发过程中至少存在以下问题:药物输注设备往往仅能单独使用,无法与其他设备进行信息传输。There are at least the following problems in the development process of related technologies: drug infusion equipment can often only be used alone and cannot transmit information with other equipment.
发明内容Contents of the invention
本申请提供了一种药物输注设备及药物输注系统,以解决药物输注设备无法进行信息传输的问题。This application provides a drug infusion device and a drug infusion system to solve the problem that the drug infusion device cannot transmit information.
根据本申请的一方面,提供了一种药物输注设备,所述药物输注设备包括:壳体、驱动装置、流动路径、数据通信部件以及至少一个处理器;所述处理器分别与所述驱动装置、所述数据通信部件电连接;所述驱动装置、所述数据通信部件以及至少一个处理器设置在所述壳体内;According to one aspect of the present application, a drug infusion device is provided. The drug infusion device includes: a housing, a driving device, a flow path, a data communication component, and at least one processor; the processor is respectively connected to the The driving device and the data communication component are electrically connected; the driving device, the data communication component and at least one processor are arranged in the housing;
所述数据通信部件,与输注控制设备通信连接,被设置为接收所述输注控制设备发送的输注控制信息,将所述输注控制信息传输至所述处理器;The data communication component is communicatively connected with the infusion control device, and is configured to receive the infusion control information sent by the infusion control device and transmit the infusion control information to the processor;
所述处理器,被设置为基于所述输注控制信息控制所述驱动装置进行工作,以将所述流动路径中的液体输出。The processor is configured to control the driving device to operate based on the infusion control information to output the liquid in the flow path.
根据本申请的另一方面,提供了一种药物输注系统,所述药物输注系统包括:输注控制设备和本申请任一实施例所述的药物输注设备;According to another aspect of the present application, a drug infusion system is provided, which includes: an infusion control device and the drug infusion device described in any embodiment of the present application;
所述输注控制设备包括数据采集部件,其中,所述数据采集部件被设置为采集输注控制信息。The infusion control device includes a data collection component, wherein the data collection component is configured to collect infusion control information.
应当理解,本部分所描述的内容并非标识本申请的实施例的关键或重要特征。本申请的其它特征将通过以下的说明书而变得容易理解。It should be understood that what is described in this section does not identify key or important features of the embodiments of the present application. Other features of the present application will become readily understood from the following description.
附图说明Description of drawings
下面将对实施例描述中所需要使用的附图作简单地介绍,下面描述中的附图仅仅是本申请的一些实施例,对于本领域普通技术人员来讲,在不付出创造性劳动的前提下,还可以根据这些附图获得其他的附图。The drawings needed to be used in the description of the embodiments will be briefly introduced below. The drawings in the following description are only some embodiments of the present application. For those of ordinary skill in the art, without exerting any creative effort, , other drawings can also be obtained based on these drawings.
图1是根据本申请实施例一提供的一种药物输注设备的结构示意图;Figure 1 is a schematic structural diagram of a drug infusion device provided according to Embodiment 1 of the present application;
图2是根据本申请实施例一提供的一种数据处理的流程示意图;Figure 2 is a schematic flow chart of data processing provided according to Embodiment 1 of the present application;
图3是根据本申请实施例一提供的一种处理器执行模块结构示意图;Figure 3 is a schematic structural diagram of a processor execution module provided according to Embodiment 1 of the present application;
图4是根据本申请实施例二提供的一种药物输注系统的结构示意图;Figure 4 is a schematic structural diagram of a drug infusion system provided according to Embodiment 2 of the present application;
图5是根据本申请实施例二提供的一种数据采集部件的结构示意图;Figure 5 is a schematic structural diagram of a data collection component provided according to Embodiment 2 of the present application;
图6是根据本申请实施例二提供的另一种药物输注系统的结构示意图;Figure 6 is a schematic structural diagram of another drug infusion system provided according to Embodiment 2 of the present application;
图7是根据本申请实施例二提供的另一种药物输注系统的结构示意图;Figure 7 is a schematic structural diagram of another drug infusion system provided according to Embodiment 2 of the present application;
图8是根据本申请实施例二提供的一种PCA控制器的结构示意图;Figure 8 is a schematic structural diagram of a PCA controller provided according to Embodiment 2 of the present application;
图9是根据本申请实施例二提供的一种输液泵的结构示意图。Figure 9 is a schematic structural diagram of an infusion pump provided according to Embodiment 2 of the present application.
具体实施方式Detailed ways
为了使本技术领域的人员更好地理解本申请方案,下面将结合本申请实施例中的附图,对本申请实施例中的技术方案进行描述,所描述的实施例仅仅是本申请一部分的实施例,而不是全部的实施例。基于本申请中的实施例,本领域普通技术人员在没有做出创造性劳动前提下所获得的所有其他实施例,都应当属于本申请保护的范围。In order to enable those in the technical field to better understand the solutions of the present application, the technical solutions in the embodiments of the present application will be described below in conjunction with the drawings in the embodiments of the present application. The described embodiments are only implementations of a part of the present application. examples, not all examples. Based on the embodiments in this application, all other embodiments obtained by those of ordinary skill in the art without creative efforts should fall within the scope of protection of this application.
需要说明的是,本申请的说明书和权利要求书及上述附图中的术语“目标”、“初始”等是用于区别类似的对象,而不必用于描述特定的顺序或先后次序。应该理解这样使用的数据在适当情况下可以互换,以便这里描述的本申请的实施例能够以除了在这里图示或描述的那些以外的顺序实施。此外,术语“包括”和“具有”以及他们的任何变形,意图在于覆盖不排他的包含,例如,包含了一系列步骤或单元的过程、方法、系统、产品或设备不必限于清楚地列出的那些步骤或单元,而是可包括没有清楚地列出的或对于这些过程、方法、产品或设备固有的其它步骤或单元。It should be noted that the terms "target", "initial", etc. in the description and claims of this application and the above-mentioned drawings are used to distinguish similar objects and are not necessarily used to describe a specific sequence or sequence. It is to be understood that the data so used are interchangeable under appropriate circumstances so that the embodiments of the application described herein can be practiced in sequences other than those illustrated or described herein. In addition, the terms "including" and "having" and any variations thereof are intended to cover non-exclusive inclusions, e.g., a process, method, system, product, or apparatus that encompasses a series of steps or units and need not be limited to those explicitly listed. Those steps or elements may instead include other steps or elements not expressly listed or inherent to the process, method, product or apparatus.
实施例一 Embodiment 1
图1为本申请实施例一提供的一种药物输注设备的结构示意图,本实施例可适用于输注控制设备对药物输注设备进行控制的情况。如图1所示,该药物输注设备,包括:壳体100、驱动装置110、流动路径120、数据通信部件130以及至少一个处理器140;处理器140分别与驱动装置110、数据通信部件130 电连接;驱动装置110、数据通信部件130以及至少一个处理器140设置在壳体100内;数据通信部件130,与输注控制设备通信连接,被设置为接收输注控制设备发送的输注控制信息,将输注控制信息传输至处理器140;处理器140,被设置为基于输注控制信息控制驱动装置110进行工作,以将流动路径120中的液体输出。Figure 1 is a schematic structural diagram of a drug infusion device provided in Embodiment 1 of the present application. This embodiment can be applied to situations where the infusion control device controls the drug infusion device. As shown in Figure 1, the drug infusion device includes: a housing 100, a driving device 110, a flow path 120, a data communication component 130, and at least one processor 140; the processor 140 is connected to the driving device 110 and the data communication component 130 respectively. Electrical connection; the driving device 110, the data communication component 130 and the at least one processor 140 are disposed in the housing 100; the data communication component 130 is communicatively connected with the infusion control device and is configured to receive the infusion control sent by the infusion control device The information transmits the infusion control information to the processor 140; the processor 140 is configured to control the driving device 110 to operate based on the infusion control information to output the liquid in the flow path 120.
在本实施例中,壳体100是指药物输注设备的壳状部件。驱动装置110是指用于驱动流动路径120中的液体输出的装置,驱动装置110与流动路径120通过液体通路连接。可选的,驱动装置110可以为泵。流动路径120是指具有存储或传输液体功能的管路。可以理解的是,图1中的流动路径120仅用于示例,流动路径120可以全部位于壳体100内,也可以部分位于壳体100外。数据通信部件130是指进行数据传输的部件。可选的,通信连接对应的通信方式包括有线通信和无线通信。示例性的,数据通信部件130可以为蓝牙、无线保真(Wireless Fidelity,WIFI)、射频识别(Radio Frequency Identification,RFID)等无线通信模块,也可以为有线通信模块。处理器140是指用于进行数据处理的电子器件,例如处理器140可以用于对信号进行模数转换、串并转换、数据加工等数据处理操作。输注控制信息是指可以用于控制驱动装置110的控制信号。In this embodiment, the housing 100 refers to the shell-shaped component of the drug infusion device. The driving device 110 refers to a device for driving the liquid output in the flow path 120, and the driving device 110 and the flow path 120 are connected through a liquid passage. Optionally, the driving device 110 may be a pump. The flow path 120 refers to a pipeline with the function of storing or transmitting liquid. It can be understood that the flow path 120 in FIG. 1 is only for example, and the flow path 120 may be entirely located inside the housing 100 or partially located outside the housing 100 . The data communication component 130 refers to a component that performs data transmission. Optionally, the communication method corresponding to the communication connection includes wired communication and wireless communication. For example, the data communication component 130 can be a wireless communication module such as Bluetooth, Wireless Fidelity (WIFI), Radio Frequency Identification (RFID), etc., or it can also be a wired communication module. The processor 140 refers to an electronic device used for data processing. For example, the processor 140 can be used to perform data processing operations such as analog-to-digital conversion, serial-to-parallel conversion, and data processing on signals. Infusion control information refers to control signals that can be used to control the driving device 110 .
示例性的,当用户在进行输液时,可以通过操作输注控制设备生成输注控制信息,输注控制设备通过有线或无线的通信方式将输注控制信息发送至药物输注设备,药物输注设备的处理器140可以根据输注控制信息控制驱动装置110进行工作,实现将流动路径120中的液体输出。For example, when the user is performing infusion, the infusion control device can generate infusion control information by operating the infusion control device, and the infusion control device sends the infusion control information to the drug infusion device through wired or wireless communication, and the drug infusion The processor 140 of the device can control the driving device 110 to operate according to the infusion control information to output the liquid in the flow path 120 .
在上述实施例的基础上,处理器140还被设置为基于数据通信部件130接收到的生理参数信息对驱动装置110进行控制。On the basis of the above embodiments, the processor 140 is further configured to control the driving device 110 based on the physiological parameter information received by the data communication component 130 .
可选的,数据通信部件130还被设置为接收生理参数信息,并将生理参数信息传输至处理器140,其中,处理器14可以根据接收的生理参数信息对驱动装置进行控制。Optionally, the data communication component 130 is also configured to receive physiological parameter information and transmit the physiological parameter information to the processor 140, where the processor 14 can control the driving device according to the received physiological parameter information.
在上述实施例的基础上,生理参数信息可以通过生理参数采集模块采集得到,生理参数采集模块可以设置在输注控制设备上,也可以分布式设置在穿戴设备、医疗设备等其他设备上。生理参数采集模块包括血压采集模块、心电采集模块、血氧采集模块、心率采集模块和按压采集模块。示例性的,血压采集模块被设置为采集输注对象的血压模拟信号;心电采集模块被设置为采集输注对象的心电模拟信号;血氧采集模块被设置为采集输注对象的血氧模拟信号;心率采集模块被设置为采集输注对象的心率模拟信号。可以理解的是,通过获取用户的生理参数信息,实现了生理参数的实时监测。Based on the above embodiments, physiological parameter information can be collected through the physiological parameter acquisition module. The physiological parameter acquisition module can be set on the infusion control device, or can be distributed on other devices such as wearable devices and medical equipment. The physiological parameter collection module includes a blood pressure collection module, an ECG collection module, a blood oxygen collection module, a heart rate collection module and a compression collection module. Exemplarily, the blood pressure acquisition module is configured to collect the blood pressure analog signal of the infusion subject; the ECG acquisition module is configured to collect the ECG analog signal of the infusion subject; and the blood oxygen acquisition module is configured to collect the blood oxygen of the infusion subject. Analog signal; the heart rate acquisition module is set to collect the heart rate analog signal of the infusion subject. It can be understood that by obtaining the user's physiological parameter information, real-time monitoring of physiological parameters is achieved.
图2是根据本实施例提供的一种数据处理的流程示意图。数据处理步骤可以包括:S10、获取生理参数信息;S20、对生理参数信息进行数据分析,得到分析结果;S30、根据分析结果调整药物输注设备的输注参数。Figure 2 is a schematic flowchart of data processing provided according to this embodiment. The data processing steps may include: S10, obtaining physiological parameter information; S20, performing data analysis on the physiological parameter information, and obtaining analysis results; S30, adjusting the infusion parameters of the drug infusion equipment according to the analysis results.
示例性的,图3是本实施例提供的一种处理器执行模块结构示意图,在处理器140接收心率、血压血氧、呼末二氧化碳(CO2)、心电等生理参数信息之后,可以通过数据分析模块141对生理参数信息进行数据分析,数据分析模块141可以为数据分析方法的封装模块,数据分析模块141可配置于处理器140中。可选的,可以根据分析结果调整药物输注设备的输注参数,并且可以通过数据通信部件130外发相关信息,相关信息可以包括分析结果、生理参数等信息。Exemplarily, FIG. 3 is a schematic structural diagram of a processor execution module provided in this embodiment. After the processor 140 receives physiological parameter information such as heart rate, blood pressure, blood oxygen, end-tidal carbon dioxide (CO2), and ECG, it can use the data to The analysis module 141 performs data analysis on the physiological parameter information. The data analysis module 141 can be a packaging module of the data analysis method. The data analysis module 141 can be configured in the processor 140 . Optionally, the infusion parameters of the drug infusion device can be adjusted according to the analysis results, and relevant information can be sent out through the data communication component 130. The relevant information can include analysis results, physiological parameters and other information.
以心率模拟信号为例进行阐述,处理器140可以对心率模拟信号进行模数转换,得到心率,若心率超出预设心率阈值或心率变化超出预设规则等,则可以暂停驱动装置110的工作或者降低驱动装置110的驱动速度等。可选的,心率变化可以为预设时间区间内的变化量、预设采样间隔间的变化量、心率变化率或者变化预测量等。预设规则可以为:预设时间区间的变化量超出预设的心率变化量阈值;或者,预设采样间隔,例如相邻两次采集到的心率的变化量或间隔2次等采样到的心率的变化量超过预设的心率变化量阈值;或者,心率变化率或心率变化预测量超过预设的变化阈值。Taking the heart rate analog signal as an example to illustrate, the processor 140 can perform analog-to-digital conversion on the heart rate analog signal to obtain the heart rate. If the heart rate exceeds a preset heart rate threshold or the heart rate change exceeds a preset rule, the work of the driving device 110 can be suspended or Reduce the driving speed of the driving device 110 or the like. Optionally, the heart rate change may be a change amount within a preset time interval, a change amount between preset sampling intervals, a heart rate change rate, a change prediction amount, etc. The preset rule can be: the change in the preset time interval exceeds the preset heart rate change threshold; or the preset sampling interval, such as the change in heart rate collected twice in a row or the heart rate sampled two times apart. The change amount exceeds the preset heart rate change threshold; or the heart rate change rate or the predicted amount of heart rate change exceeds the preset change threshold.
在上述实施例的基础上,数据通信部件130还被设置为将生理参数信息和预处理后的生理参数信息中的至少之一发送至云端服务器。Based on the above embodiments, the data communication component 130 is further configured to send at least one of the physiological parameter information and the preprocessed physiological parameter information to the cloud server.
预处理后的生理参数信息是指经预处理操作的生理参数信息。预处理操作包括筛选、清洗、归一化等。需要说明的是,上传至云端服务器的生理参数信息和预处理后的生理参数信息中的至少之一可以用于大数据分析处理。The preprocessed physiological parameter information refers to the physiological parameter information that has been preprocessed. Preprocessing operations include screening, cleaning, normalization, etc. It should be noted that at least one of the physiological parameter information uploaded to the cloud server and the preprocessed physiological parameter information can be used for big data analysis and processing.
在上述实施例的基础上,处理器140还被设置为:基于预设判断规则,对所述输注控制信息进行判断;在所述输注控制信息不符合所述预设判断规则的情况下,将当前控制操作确定为无效操作,并生成报警信号。On the basis of the above embodiments, the processor 140 is further configured to: judge the infusion control information based on the preset judgment rules; when the infusion control information does not comply with the preset judgment rules , determine the current control operation as an invalid operation, and generate an alarm signal.
在本实施例中,预设判断规则是指预先设置的控制信号判断规则,示例性的,预设判断规则可以为阈值判断规则,例如,接收到的输注控制信息的频率为A,预设判断规则对应的频率范围为B-C,若A不在B-C频率范围内,则确定当前控制操作为无效操作。无效操作是指未生效的操作。In this embodiment, the preset judgment rule refers to a preset control signal judgment rule. For example, the preset judgment rule can be a threshold judgment rule. For example, the frequency of the received infusion control information is A, and the preset judgment rule is A. The frequency range corresponding to the judgment rule is B-C. If A is not within the B-C frequency range, the current control operation is determined to be an invalid operation. Invalid operations refer to operations that have not taken effect.
在本实施例中,输注控制信息可以包括按压信息、手写输入信息、手势信息等。可选的,输注控制信息包括按压频率、按压次数和按压时长中的至少之一;相应的,预设判断规则可以为按压判断规则,无效操作可以为无效按压。In this embodiment, the infusion control information may include pressing information, handwriting input information, gesture information, etc. Optionally, the infusion control information includes at least one of the compression frequency, the number of compressions, and the compression duration; accordingly, the preset judgment rule can be a compression judgment rule, and the invalid operation can be invalid compression.
在一些实施例中,药物输注设备可以根据按压频率、按压次数和按压时长 中的至少之一生成输注参数调整信息,以基于输注参数调整信息对驱动装置110进行控制。可选的,输注参数调整信息与按压频率、按压次数和按压时长可以具有对应关系,例如,输注参数调整信息可以为用药剂量,按压一次对应提升对应A剂量,按压两次对应提升对应B剂量。输注参数是指输液泵的工作参数,可以包括用药量、输注速度等。当然,还可以是若按压一次,则对应提升或降低对应的剂量;或者,若长时间按压(例如按压时长超过5秒)控制按键,则产生暂停或启动等控制信号,以实现控制输液泵停止运行。In some embodiments, the drug infusion device may generate infusion parameter adjustment information based on at least one of the compression frequency, the number of compressions, and the compression duration to control the driving device 110 based on the infusion parameter adjustment information. Optionally, the infusion parameter adjustment information can have a corresponding relationship with the compression frequency, the number of compressions, and the compression duration. For example, the infusion parameter adjustment information can be the dosage of medication. One press corresponds to an increase in dose A, and two presses correspond to an increase in dose B. dose. Infusion parameters refer to the working parameters of the infusion pump, which can include drug dosage, infusion speed, etc. Of course, it can also be that if the control button is pressed once, the corresponding dose will be increased or decreased; or, if the control button is pressed for a long time (for example, for more than 5 seconds), a control signal such as pause or start will be generated to control the infusion pump to stop. run.
本申请实施例的技术方案,通过药物输注设备的数据通信部件,实现了输注控制设备与药物输注设备之间的信息传输,解决了药物输注设备无法进行信息传输的问题,从而实现了药物输注设备的控制。The technical solution of the embodiment of the present application realizes information transmission between the infusion control device and the drug infusion device through the data communication component of the drug infusion device, solving the problem that the drug infusion device cannot transmit information, thereby achieving Control of drug infusion equipment.
实施例二 Embodiment 2
图4为本申请实施例二提供的一种药物输注系统的结构示意图。如图4所示,药物输注系统包括:输注控制设备200和本申请任一实施例所述的药物输注设备;输注控制设备200包括数据采集部件210,其中,数据采集部件210被设置为采集输注控制信息。Figure 4 is a schematic structural diagram of a drug infusion system provided in Embodiment 2 of the present application. As shown in Figure 4, the drug infusion system includes: an infusion control device 200 and the drug infusion device described in any embodiment of the present application; the infusion control device 200 includes a data acquisition component 210, wherein the data acquisition component 210 is Set to collect infusion control information.
在本实施例中,数据采集部件210可以设置在设备本体上,也可以分布式设置在其他设备上。In this embodiment, the data collection component 210 can be disposed on the device body, or can be disposed on other devices in a distributed manner.
可选的,数据采集部件210还被设置为采集用户的生理参数信息。Optionally, the data collection component 210 is also configured to collect the user's physiological parameter information.
在本实施例中,图5是本实施例提供的一种数据采集部件的结构示意图,数据采集部件210可以包括控制信号采集模块211和生理参数采集模块212。其中,控制信号采集模块211被设置为采集输注控制信息,控制信号采集模块211可以为按钮或按键等形式。生理参数采集模块212被设置为采集用户的生理参数信息。In this embodiment, FIG. 5 is a schematic structural diagram of a data collection component provided in this embodiment. The data collection component 210 may include a control signal collection module 211 and a physiological parameter collection module 212. Among them, the control signal acquisition module 211 is configured to collect infusion control information, and the control signal acquisition module 211 can be in the form of a button or a key. The physiological parameter collection module 212 is configured to collect the user's physiological parameter information.
在上述实施例的基础上,图6是本实施例提供的另一种药物输注系统的结构示意图,输注控制设备200还包括:身份识别模块220,被设置为采集用户的身份验证信息,身份验证信息用于验证用户身份。Based on the above embodiment, Figure 6 is a schematic structural diagram of another drug infusion system provided by this embodiment. The infusion control device 200 also includes: an identity recognition module 220, which is configured to collect the user's identity verification information, Authentication information is used to verify the user's identity.
身份识别模块220是指进行身份验证的模块,身份识别模块220的验证方式可以包括密码验证、操控手势验证、指纹验证、面部信息验证、无线手环验证等。可以理解的是,无线手环可以设置有近场通讯(Near Field Communication,NFC)等近场通信功能模块,通过NFC等近场通信功能模块可以实现身份验证。The identity recognition module 220 refers to a module that performs identity verification. The verification methods of the identity recognition module 220 may include password verification, control gesture verification, fingerprint verification, facial information verification, wireless bracelet verification, etc. It is understandable that the wireless bracelet can be equipped with near field communication function modules such as Near Field Communication (NFC), and identity authentication can be achieved through NFC and other near field communication function modules.
在一些实施例中,身份识别模块220被设置为采集用户的身份验证信息,并将身份验证信息发送至数据采集部件210或输注控制设备200的数据处理器 230;相应的,数据处理器230或数据采集部件210还被设置为接收身份识别模块220发送的身份验证信息,将身份验证信息与预留验证信息进行匹配,若身份验证信息匹配成功,则身份验证成功,表明当前输注控制设备200的操作者有权操作;若身份验证信息未匹配成功,则身份验证失败,表明当前输注控制设备200的操作者无权操作。In some embodiments, the identity recognition module 220 is configured to collect the user's identity verification information, and send the identity verification information to the data collection component 210 or the data processor 230 of the infusion control device 200; accordingly, the data processor 230 Or the data collection component 210 is also configured to receive the identity verification information sent by the identity recognition module 220, and match the identity verification information with the reserved verification information. If the identity verification information matches successfully, the identity verification is successful, indicating that the current infusion control device The operator of 200 has the right to operate; if the identity verification information does not match successfully, the identity verification fails, indicating that the operator of the current infusion control device 200 does not have the right to operate.
在一些实施例中,身份识别模块220被设置为采集用户的身份验证信息,并将身份验证信息传输至药物输注设备;相应的,药物输注设备接收身份验证信息,将身份验证信息与预留验证信息进行匹配,若身份验证信息匹配成功,则身份验证成功,表明当前输注控制设备200的操作者有权操作,并将成功验证结果返回输注控制设备200;若身份验证信息未匹配成功,则身份验证失败,表明当前输注控制设备200的操作者无权操作。相应的,数据处理器230或数据采集部件210只有接收到药物输注设备返回的成功验证结果,才判断身份验证成功。In some embodiments, the identity recognition module 220 is configured to collect the user's identity verification information and transmit the identity verification information to the drug infusion device; accordingly, the drug infusion device receives the identity verification information and compares the identity verification information with the predetermined Verification information is left for matching. If the identity verification information matches successfully, the identity verification is successful, indicating that the operator of the current infusion control device 200 has the authority to operate, and the successful verification result is returned to the infusion control device 200; if the identity verification information does not match If successful, the identity verification fails, indicating that the current operator of the infusion control device 200 does not have the right to operate. Correspondingly, the data processor 230 or the data collection component 210 determines that the identity verification is successful only after receiving a successful verification result returned by the drug infusion device.
在一些实施例中,控制按键上可以集成有指纹模块,即用户在按压控制按键的同时即可完成用户身份的验证,可用于确认操作用户是否为本人或者授权人员操作。In some embodiments, the control button can be integrated with a fingerprint module, that is, the user can complete user identity verification while pressing the control button, which can be used to confirm whether the operating user is himself or an authorized person.
在一些实施例中,身份识别模块220可以为RFID模块,通过RFID模块对操作用户的工牌或者手环进行识别,得到用户身份,用户身份可以包括医护工作者、病人等。In some embodiments, the identity recognition module 220 may be an RFID module. The RFID module identifies the user's badge or bracelet to obtain the user's identity. The user's identity may include medical workers, patients, etc.
在上述实施例的基础上,输注控制设备200的数据处理器230是被设置为:若基于身份验证信息确定当前操作人员的身份验证成功,则接收数据采集部件210发送的药物输注设备控制信号,并基于药物输注设备控制信号确定输注控制信息;或者,数据采集部件210是被设置为:若基于身份验证信息确定当前操作人员的身份验证成功,则采集用户输入的药物输注设备控制信号,并将药物输注设备控制信号发送至数据处理器230。Based on the above embodiment, the data processor 230 of the infusion control device 200 is configured to: if it is determined that the identity verification of the current operator is successful based on the identity verification information, receive the drug infusion device control sent by the data acquisition component 210 signal, and determine the infusion control information based on the drug infusion equipment control signal; alternatively, the data collection component 210 is set to: if it is determined that the identity verification of the current operator is successful based on the identity verification information, collect the drug infusion equipment input by the user. control signal, and sends the drug infusion device control signal to the data processor 230 .
需要说明的是,数据采集部件210或数据处理器230都可以用于验证当前操作人员的身份。It should be noted that either the data collection component 210 or the data processor 230 can be used to verify the identity of the current operator.
可以理解的是,在医疗场景下,患者、患者家属和医生等都可能对输注控制设备200进行控制,为了保证输液的安全性,本实施例对不同操作人员的操作权限进行划分,享有不同操作权限的人员可以对药物输注设备进行控制的参数项至少部分不同。可选的,在获取身份验证信息之后,可以根据身份验证信息确定操作人员的类型,例如当操作人员的类型为医生时,确定医生对应的操作权限,并且激活操作权限对应的输注控制设备功能,以便医生对药物输注设备进行调节。例如,医生的操作权限最高,可以对药物输注设备进行所有控制 操作;患者次之,可以对药物输注设备的输液速度、开启、停止进行控制;患者家属的权限最低,仅能暂停药物输注设备。当然,不同操作人员的操作权限可以根据实际需要划分。It can be understood that in a medical scenario, patients, patients' family members, doctors, etc. may all control the infusion control device 200. In order to ensure the safety of infusion, this embodiment divides the operating authority of different operators and enjoys different rights. Personnel with operating authority can control at least some of the parameters of the drug infusion equipment. Optionally, after obtaining the identity verification information, the type of operator can be determined based on the identity verification information. For example, when the type of operator is a doctor, the corresponding operating authority of the doctor is determined, and the infusion control device function corresponding to the operating authority is activated. , so that doctors can adjust the drug infusion equipment. For example, the doctor has the highest operating authority and can perform all control operations on the drug infusion equipment; the patient has the second highest authority and can control the infusion speed, start and stop of the drug infusion equipment; the patient's family has the lowest authority and can only suspend drug infusion. Note equipment. Of course, the operating permissions of different operators can be divided according to actual needs.
可选的,还可以针对不同操作人员提供不同的身份验证方式。例如,针对患者可以采用指纹验证,针对医生可以采用密码验证等,身份验证方式可以针对实际需要设置。Optionally, different authentication methods can also be provided for different operators. For example, fingerprint verification can be used for patients, password verification can be used for doctors, etc. The identity verification method can be set according to actual needs.
当然,上述基于身份验证信息确定当前操作人员的操作权限,激活操作权限对应的输注控制设备功能的步骤也可以由数据采集部件210执行。即在上述实施例的基础上,数据采集部件210还可以被设置为:基于身份验证信息确定当前操作人员的操作权限,激活操作权限对应的输液泵控制设备功能。例如,数据采集部件210只有判断当前操作人员输入的药物输注设备控制信号符合其操作权限,才将药物输注设备控制信号发送至数据处理器。此时,数据处理器230则只需要根据数据采集部件210发送的药物输注设备控制信号,并基于药物输注设备控制信号确定输注控制信息。Of course, the above-mentioned steps of determining the operating authority of the current operator based on the identity verification information and activating the infusion control device function corresponding to the operating authority can also be performed by the data collection component 210. That is, based on the above embodiments, the data collection component 210 can also be configured to: determine the operating authority of the current operator based on the identity verification information, and activate the infusion pump control device function corresponding to the operating authority. For example, the data collection component 210 only sends the control signal of the drug infusion device to the data processor if it determines that the drug infusion device control signal input by the current operator complies with its operating authority. At this time, the data processor 230 only needs to determine the infusion control information based on the drug infusion equipment control signal sent by the data acquisition component 210.
在上述实施例的基础上,图7是本实施例提供的另一种药物输注系统的结构示意图,输注控制设备200还包括信息输出部件240,可选的,信息输出部件240包括显示屏、提示灯和扬声器中的至少之一。Based on the above embodiment, FIG. 7 is a schematic structural diagram of another drug infusion system provided by this embodiment. The infusion control device 200 also includes an information output component 240. Optionally, the information output component 240 includes a display screen. , at least one of the indicator light and the speaker.
可选的,显示屏被设置为显示当前输注参数和报警信息内容中的至少之一;提示灯被设置为响应于报警信号,切换至亮灯状态或者切换至报警灯颜色;扬声器被设置为输出当前输注参数,和/或,响应于报警信号,输出报警音频。在一些实施例中,信息输出部件240还可以包括震动部件,震动部件被设置为产生震动,以反馈用户的操作情况,例如,震动部件可以为马达等。Optionally, the display screen is set to display at least one of the current infusion parameters and alarm information content; the prompt light is set to switch to a light state or the alarm light color in response to the alarm signal; the speaker is set to Current infusion parameters are output, and/or, in response to the alarm signal, alarm audio is output. In some embodiments, the information output component 240 may also include a vibration component, which is configured to generate vibration to feedback the user's operation. For example, the vibration component may be a motor or the like.
在一些实施例中,药物输注设备也可以包括身份识别模块和信息输出部件中的至少之一,其实现方式与输注控制设备200中的身份识别模块和信息输出部件相似或相同。In some embodiments, the drug infusion device may also include at least one of an identity recognition module and an information output component, the implementation of which is similar or identical to the identity recognition module and the information output component in the infusion control device 200 .
可以理解的是,在操作输注控制设备200时,输注控制设备200可以通过信息输出部件进行声光、震动等方式的反馈,药物输注设备也可以展示相关操作反馈信息。It can be understood that when operating the infusion control device 200, the infusion control device 200 can provide feedback in the form of sound, light, vibration, etc. through the information output component, and the drug infusion device can also display relevant operation feedback information.
示例性的,图8为本申请实施例提供的一种PCA控制器的结构示意图。PCA(Patient controlled analgesia)控制器(即输注控制设备)包括生理参数采集模块1、手环2(可用于采集生理参数信息)、连接线3、电池4、PCA键5(即控制按键)、指纹识别模块6(即身份识别模块)、显示屏7、提示部件8,提示部件8可以包括报警(提示)灯和扬声器等。该输注控制设备可以集中采集 用户的生理参数信息,并且通过指纹识别模块可以验证用户身份,从而可以减少PCA控制器误触的风险。For example, FIG. 8 is a schematic structural diagram of a PCA controller provided by an embodiment of the present application. PCA (Patient controlled analgesia) controller (i.e. infusion control device) includes physiological parameter collection module 1, bracelet 2 (can be used to collect physiological parameter information), connecting cable 3, battery 4, PCA key 5 (i.e. control button), Fingerprint recognition module 6 (i.e. identity recognition module), display screen 7, prompt component 8, prompt component 8 may include an alarm (prompt) light and a speaker, etc. The infusion control device can centrally collect the user's physiological parameter information and verify the user's identity through the fingerprint recognition module, thereby reducing the risk of accidental touch of the PCA controller.
示例性的,图9为本申请实施例提供的一种输液泵的结构示意图。输液泵(即药物输注设备)包括开关(开机(ON)/关机(OFF))、剂量控制按键(Dose)、驱动装置、数据通信部件以及至少一个处理器。输液泵可以通过数据通信部件与多种医疗设备通信连接,实现生理参数信息的集中采集,避免数据的缺失。输液泵可以对生理参数信息进行预处理,并将预处理后的生理参数信息上传至云端服务器,以完成大数据分析处理。Exemplarily, FIG. 9 is a schematic structural diagram of an infusion pump provided by an embodiment of the present application. The infusion pump (i.e., drug infusion equipment) includes a switch (ON/OFF), a dose control button (Dose), a driving device, a data communication component, and at least one processor. The infusion pump can communicate with a variety of medical equipment through data communication components to achieve centralized collection of physiological parameter information and avoid data loss. The infusion pump can preprocess physiological parameter information and upload the preprocessed physiological parameter information to the cloud server to complete big data analysis and processing.
本申请实施例的技术方案,通过药物输注设备的数据通信部件,实现了输注控制设备与药物输注设备之间的信息传输,解决了药物输注设备无法进行数据传输的问题,从而实现了药物输注设备的控制。The technical solution of the embodiment of the present application realizes information transmission between the infusion control device and the drug infusion device through the data communication component of the drug infusion device, solving the problem that the drug infusion device cannot transmit data, thereby achieving Control of drug infusion equipment.
应该理解,可以使用上面所示的各种形式的流程,重新排序、增加或删除步骤。例如,本申请中记载的各步骤可以并行地执行,也可以顺序地执行,也可以不同的次序执行,只要能够实现本申请的技术方案所期望的结果。It should be understood that various forms of the process shown above may be used, with steps reordered, added or deleted. For example, each step described in this application can be executed in parallel, sequentially, or in a different order, as long as the desired results of the technical solution of this application can be achieved.

Claims (10)

  1. 一种药物输注设备,所述药物输注设备包括:壳体、驱动装置、流动路径、数据通信部件以及至少一个处理器;所述处理器分别与所述驱动装置、所述数据通信部件电连接;所述驱动装置、所述数据通信部件以及至少一个处理器设置在所述壳体内;A drug infusion device, the drug infusion device includes: a housing, a driving device, a flow path, a data communication component and at least one processor; the processor is electrically connected to the driving device and the data communication component respectively. Connection; the driving device, the data communication component and at least one processor are arranged in the housing;
    所述数据通信部件,与输注控制设备通信连接,被设置为接收所述输注控制设备发送的输注控制信息,将所述输注控制信息传输至所述处理器;The data communication component is communicatively connected with the infusion control device, and is configured to receive the infusion control information sent by the infusion control device and transmit the infusion control information to the processor;
    所述处理器,被设置为基于所述输注控制信息控制所述驱动装置进行工作,以将所述流动路径中的液体输出。The processor is configured to control the driving device to operate based on the infusion control information to output the liquid in the flow path.
  2. 根据权利要求1所述的药物输注设备,其中,所述通信连接对应的通信方式包括有线通信和无线通信。The drug infusion device according to claim 1, wherein the communication mode corresponding to the communication connection includes wired communication and wireless communication.
  3. 根据权利要求1所述的药物输注设备,其中,所述处理器还被设置为基于所述数据通信部件接收到的生理参数信息对所述驱动装置进行控制。The drug infusion device according to claim 1, wherein the processor is further configured to control the driving device based on physiological parameter information received by the data communication component.
  4. 根据权利要求3所述的药物输注设备,其中,所述数据通信部件还被设置为将所述生理参数信息和预处理后的生理参数信息中的至少之一发送至云端服务器。The drug infusion device according to claim 3, wherein the data communication component is further configured to send at least one of the physiological parameter information and preprocessed physiological parameter information to a cloud server.
  5. 根据权利要求1所述的药物输注设备,其中,所述处理器还被设置为:The drug infusion device of claim 1, wherein the processor is further configured to:
    基于预设判断规则,对所述输注控制信息进行判断;Based on preset judgment rules, judge the infusion control information;
    在所述输注控制信息不符合所述预设判断规则的情况下,将当前控制操作确定为无效操作,并生成报警信号。When the infusion control information does not comply with the preset judgment rule, the current control operation is determined to be an invalid operation, and an alarm signal is generated.
  6. 根据权利要求5所述的药物输注设备,其中,所述输注控制信息包括按压频率、按压次数和按压时长中的至少之一。The drug infusion device according to claim 5, wherein the infusion control information includes at least one of compression frequency, compression number and compression duration.
  7. 一种药物输注系统,所述药物输注系统包括:输注控制设备和权利要求1-6中任一项所述的药物输注设备;A drug infusion system, the drug infusion system includes: an infusion control device and the drug infusion device according to any one of claims 1-6;
    所述输注控制设备包括数据采集部件,其中,所述数据采集部件被设置为采集输注控制信息。The infusion control device includes a data collection component, wherein the data collection component is configured to collect infusion control information.
  8. 根据权利要求7所述的药物输注系统,其中,所述数据采集部件还被设置为采集用户的生理参数信息。The drug infusion system according to claim 7, wherein the data collection component is further configured to collect physiological parameter information of the user.
  9. 根据权利要求7所述的药物输注系统,其中,所述输注控制设备还包括:The drug infusion system of claim 7, wherein the infusion control device further includes:
    身份识别模块,被设置为采集用户的身份验证信息,所述身份验证信息用于验证用户身份。The identity recognition module is configured to collect the user's identity verification information, and the identity verification information is used to verify the user's identity.
  10. 根据权利要求7所述的药物输注系统,其中,所述输注控制设备还包括 信息输出部件,其中,所述信息输出部件包括显示屏、提示灯和扬声器中的至少之一。The drug infusion system according to claim 7, wherein the infusion control device further includes an information output component, wherein the information output component includes at least one of a display screen, a prompt light, and a speaker.
PCT/CN2022/113979 2022-08-22 2022-08-22 Drug infusion device and drug infusion system WO2024040394A1 (en)

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