WO2024040394A1 - Dispositif de perfusion de médicament et système de perfusion de médicament - Google Patents

Dispositif de perfusion de médicament et système de perfusion de médicament 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
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English (en)
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
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
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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 CN202280004926.0A priority Critical patent/CN116096442A/zh
Priority to PCT/CN2022/113979 priority patent/WO2024040394A1/fr
Publication of WO2024040394A1 publication Critical patent/WO2024040394A1/fr

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    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B5/00—Measuring for diagnostic purposes; Identification of persons
    • A61B5/02—Detecting, 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
    • A61B5/021—Measuring pressure in heart or blood vessels
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B5/00—Measuring for diagnostic purposes; Identification of persons
    • A61B5/145—Measuring characteristics of blood in vivo, e.g. gas concentration, pH value; Measuring characteristics of body fluids or tissues, e.g. interstitial fluid, cerebral tissue
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B5/00—Measuring for diagnostic purposes; Identification of persons
    • A61B5/24—Detecting, measuring or recording bioelectric or biomagnetic signals of the body or parts thereof
    • A61B5/316—Modalities, i.e. specific diagnostic methods
    • A61B5/318—Heart-related electrical modalities, e.g. electrocardiography [ECG]
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M5/00—Devices for bringing media into the body in a subcutaneous, intra-vascular or intramuscular way; Accessories therefor, e.g. filling or cleaning devices, arm-rests
    • A61M5/14—Infusion devices, e.g. infusing by gravity; Blood infusion; Accessories therefor
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M5/00—Devices for bringing media into the body in a subcutaneous, intra-vascular or intramuscular way; Accessories therefor, e.g. filling or cleaning devices, arm-rests
    • A61M5/14—Infusion devices, e.g. infusing by gravity; Blood infusion; Accessories therefor
    • A61M5/142—Pressure infusion, e.g. using pumps
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M5/00—Devices for bringing media into the body in a subcutaneous, intra-vascular or intramuscular way; Accessories therefor, e.g. filling or cleaning devices, arm-rests
    • A61M5/14—Infusion devices, e.g. infusing by gravity; Blood infusion; Accessories therefor
    • A61M5/168—Means for controlling media flow to the body or for metering media to the body, e.g. drip meters, counters ; Monitoring media flow to the body
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M5/00—Devices for bringing media into the body in a subcutaneous, intra-vascular or intramuscular way; Accessories therefor, e.g. filling or cleaning devices, arm-rests
    • A61M5/14—Infusion devices, e.g. infusing by gravity; Blood infusion; Accessories therefor
    • A61M5/168—Means for controlling media flow to the body or for metering media to the body, e.g. drip meters, counters ; Monitoring media flow to the body
    • A61M5/172—Means for controlling media flow to the body or for metering media to the body, e.g. drip meters, counters ; Monitoring media flow to the body 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

L'invention concerne un dispositif de perfusion de médicament et un système de perfusion de médicament. Le dispositif de perfusion de médicament comprend un boîtier, un appareil d'entraînement, un trajet d'écoulement, un composant de communication de données et au moins un processeur. Le processeur est connecté séparément et électriquement à l'appareil d'entraînement et au composant de communication de données. L'appareil d'entraînement, le composant de communication de données et le ou les processeurs sont disposés dans le boîtier. Le composant de communication de données est en connexion de communication avec un dispositif de commande de perfusion, et est configuré pour recevoir des informations de commande de perfusion envoyées par le dispositif de commande de perfusion et transmettre les informations de commande de perfusion au processeur. Le processeur est configuré pour commander l'appareil d'entraînement pour qu'il fonctionne sur la base des informations de commande de perfusion de façon à délivrer un liquide dans le trajet d'écoulement.
PCT/CN2022/113979 2022-08-22 2022-08-22 Dispositif de perfusion de médicament et système de perfusion de médicament WO2024040394A1 (fr)

Priority Applications (2)

Application Number Priority Date Filing Date Title
CN202280004926.0A CN116096442A (zh) 2022-08-22 2022-08-22 药物输注设备及药物输注系统
PCT/CN2022/113979 WO2024040394A1 (fr) 2022-08-22 2022-08-22 Dispositif de perfusion de médicament et système de perfusion de médicament

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PCT/CN2022/113979 WO2024040394A1 (fr) 2022-08-22 2022-08-22 Dispositif de perfusion de médicament et système de perfusion de médicament

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Citations (5)

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Publication number Priority date Publication date Assignee Title
CN201519339U (zh) * 2009-03-10 2010-07-07 中山大学 危重监护及输液控制诊疗一体化系统
CN102122364A (zh) * 2011-02-22 2011-07-13 电子科技大学 一种基于rfid无线通信的输液监护系统
CN108430539A (zh) * 2015-09-23 2018-08-21 皇家飞利浦有限公司 智能注射器:监测医学介入信息
CN113648484A (zh) * 2021-09-06 2021-11-16 北京航空航天大学 一种便携式靶控输注静脉麻醉装置及靶控输注控制方法
CN114496153A (zh) * 2020-11-12 2022-05-13 德尔格制造股份两合公司 包括控制向患者给药的设备的系统、方法和计算机程序

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN201519339U (zh) * 2009-03-10 2010-07-07 中山大学 危重监护及输液控制诊疗一体化系统
CN102122364A (zh) * 2011-02-22 2011-07-13 电子科技大学 一种基于rfid无线通信的输液监护系统
CN108430539A (zh) * 2015-09-23 2018-08-21 皇家飞利浦有限公司 智能注射器:监测医学介入信息
CN114496153A (zh) * 2020-11-12 2022-05-13 德尔格制造股份两合公司 包括控制向患者给药的设备的系统、方法和计算机程序
CN113648484A (zh) * 2021-09-06 2021-11-16 北京航空航天大学 一种便携式靶控输注静脉麻醉装置及靶控输注控制方法

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