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WO2020132813A1 - Procédé de surveillance de signe physiologique pour lésion cranio-cérébrale et dispositif de surveillance médicale - Google Patents

Procédé de surveillance de signe physiologique pour lésion cranio-cérébrale et dispositif de surveillance médicale Download PDF

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Publication number
WO2020132813A1
WO2020132813A1 PCT/CN2018/123122 CN2018123122W WO2020132813A1 WO 2020132813 A1 WO2020132813 A1 WO 2020132813A1 CN 2018123122 W CN2018123122 W CN 2018123122W WO 2020132813 A1 WO2020132813 A1 WO 2020132813A1
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WO
WIPO (PCT)
Prior art keywords
craniocerebral injury
monitoring
physiological signs
display
interface
Prior art date
Legal status (The legal status 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 status listed.)
Ceased
Application number
PCT/CN2018/123122
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English (en)
Chinese (zh)
Inventor
卿磊
王澄
唐小成
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Shenzhen Mindray Bio Medical Electronics Co Ltd
Original Assignee
Shenzhen Mindray Bio Medical Electronics Co Ltd
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.)
Filing date
Publication date
Application filed by Shenzhen Mindray Bio Medical Electronics Co Ltd filed Critical Shenzhen Mindray Bio Medical Electronics Co Ltd
Priority to PCT/CN2018/123122 priority Critical patent/WO2020132813A1/fr
Priority to CN201880098526.4A priority patent/CN112839564B/zh
Publication of WO2020132813A1 publication Critical patent/WO2020132813A1/fr
Anticipated expiration legal-status Critical
Ceased legal-status Critical Current

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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
    • 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 for evaluating the cardiovascular system, e.g. pulse, heart rate, blood pressure or blood flow
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B5/00—Measuring for diagnostic purposes; Identification of persons
    • A61B5/03—Measuring fluid pressure within the body other than blood pressure, e.g. cerebral pressure ; Measuring pressure in body tissues or organs

Definitions

  • the invention relates to the field of medical monitoring, in particular to a method and medical monitoring device for monitoring physiological signs of craniocerebral injury.
  • the monitor can synchronously and continuously monitor the patient's ECG, blood pressure, breathing and body temperature and other parameters, providing a good means for medical staff to grasp the patient's condition in a comprehensive, intuitive and timely manner.
  • monitors With the continuous development of monitors, the display interface of monitors is becoming more and more abundant.
  • Current monitors usually provide real-time patient parameters and waveform monitoring information on the main interface, and list all historical data of monitoring parameters in the review menu.
  • Doctors need to call up the review menu on the monitor during ward rounds, and then select the required parameters from many monitoring parameters for viewing and evaluation, and search and analyze system by system, which is tedious and time-consuming.
  • the present invention provides a method for monitoring physiological signs of craniocerebral injury, including:
  • physiological signs related to the craniocerebral injury of the monitored object where the physiological signs related to the craniocerebral injury include at least blood pressure and body temperature;
  • a dedicated monitoring interface for craniocerebral injury Displaying a dedicated monitoring interface for craniocerebral injury, wherein the dedicated monitoring interface for craniocerebral injury includes at least a first display area;
  • the waveform monitoring information corresponding to the physiological signs related to the craniocerebral injury is displayed on the first display area.
  • the invention provides a medical monitoring device, including:
  • a display configured to display information
  • Memory stores program instructions
  • a processor configured to execute the program instructions to implement the following method steps:
  • physiological signs related to the craniocerebral injury of the monitored object where the physiological signs related to the craniocerebral injury include at least blood pressure and body temperature;
  • a dedicated monitoring interface for craniocerebral injury Displaying a dedicated monitoring interface for craniocerebral injury, wherein the dedicated monitoring interface for craniocerebral injury includes at least a first display area;
  • the waveform monitoring information corresponding to the physiological signs related to the craniocerebral injury is displayed on the first display area.
  • the present invention provides a computer program product containing instructions, which when run on a computer, causes the computer to execute the method provided according to the first aspect of the present invention.
  • 1 is a schematic flowchart of a method for monitoring physiological signs of craniocerebral injury
  • FIG. 2 is a schematic diagram of a dedicated monitoring interface for craniocerebral injury of medical monitoring equipment
  • FIG. 3 is a schematic diagram of the doctor’s order display area on the medical monitoring equipment
  • Figure 4 is a schematic diagram of the display interface of the GCS scoring menu
  • Figure 5 is the overall schematic diagram of the monitoring interface of the medical monitoring equipment
  • FIG. 6 is a schematic structural diagram of a medical monitoring device.
  • the medical monitoring equipment mentioned in the embodiments of the present invention is not limited to a monitor, but may also be an invasive/non-invasive ventilator, anesthesia machine, nurse station, central station and other devices with monitoring functions.
  • the physiological sign monitoring method for craniocerebral injury in the present invention includes:
  • Step 101 Obtain the physiological signs of the monitored object related to the craniocerebral injury.
  • the physiological signs related to the craniocerebral injury include at least blood pressure and body temperature.
  • the medical monitoring device can obtain multiple different types of physiological signs of the monitored object according to the medical order information or configuration information, which includes a set of craniocerebral injury parameters composed of physiological signs related to craniocerebral injury, specifically
  • the craniocerebral injury parameter set includes at least blood pressure and body temperature, where the blood pressure can be non-invasive blood pressure, arterial pressure, central venous pressure, etc.
  • the physiological sign parameters related to craniocerebral injury can also include respiration rate ( respiration, rate (RR), intracranial pressure (ICP), bispectral index (BIS), etc.
  • respiration rate respiration, rate (RR)
  • ICP intracranial pressure
  • BIOS bispectral index
  • the medical monitoring device can divide the physiological signs into different types of parameter sets according to the physiological information characterized by various physiological signs.
  • the craniocerebral injury parameter set there can be other types of parameter sets, for example, It can also be divided into basic vital signs parameter sets, hemodynamic (circulatory system) parameter sets, infection parameter sets, respiratory ventilation (respiratory system) parameter sets, nutrient metabolism parameter sets, etc.
  • the specific classification of physiological sign parameters Be limited.
  • Step 102 Obtain monitoring data corresponding to physiological signs related to craniocerebral injury.
  • the medical monitoring device can acquire the acquisition signal of the physiological signs related to the craniocerebral injury through a sensor connected to the human body, and finally obtain real-time monitoring data of the physiological signs related to the craniocerebral injury.
  • the medical monitoring device may also obtain monitoring data corresponding to the physiological signs related to the craniocerebral injury from other devices.
  • the medical monitoring device is a central station
  • the central station may obtain monitoring data corresponding to physiological signs related to craniocerebral injury from the bedside monitor.
  • the monitoring data of the physiological signs in the parameter set of the subject’s brain injury within a recent period of time may be acquired, for example, the last 8 hours, the last 24 hours, and so on.
  • Step 103 Generate waveform monitoring information corresponding to the physiological signs related to the craniocerebral injury based on the monitoring data corresponding to the physiological signs related to the craniocerebral injury.
  • the medical monitoring device may generate waveform monitoring information corresponding to the physiological signs in the craniocerebral injury parameter set, respectively.
  • the waveform monitoring information may include waveform display information and numerical value display information
  • the waveform display information may include a physiological sign signal analog waveform chart and a physiological sign parameter trend chart.
  • Step 104 Display a dedicated monitoring interface for craniocerebral injury, wherein the dedicated monitoring interface for craniocerebral injury includes at least a first display area.
  • the dedicated monitoring interface for craniocerebral injury can be one of the display areas in the main monitoring interface of the medical monitoring device or a pop-up interface suspended on the main monitoring interface, where the dedicated monitoring for craniocerebral injury
  • the interface may cover the display information in the main monitoring interface, or it may not cover the display information in the main monitoring interface.
  • Step 105 Display the waveform monitoring information corresponding to the physiological signs related to the craniocerebral injury in the first display area.
  • the medical monitoring device may display the waveform monitoring information corresponding to the physiological signs related to the craniocerebral injury in the first display area.
  • the medical monitoring device may acquire the physiological signs in the craniocerebral injury parameter set related to the craniocerebral injury, and obtain the monitoring data corresponding to the physiological signs in the craniocerebral injury parameter set, and then, based on the monitoring data, Generate waveform monitoring information corresponding to physiological signs in the craniocerebral injury parameter set, and display a dedicated monitoring interface for craniocerebral injury.
  • the dedicated monitoring interface for craniocerebral injury includes at least a first display area, and further, display the craniocerebral injury parameter set in the first display area Waveform monitoring information corresponding to the physiological signs in the above manner, in addition to displaying the waveform of each physiological sign parameter, the medical monitoring equipment can also provide a dedicated monitoring interface for craniocerebral injury, and display the data associated with the craniocerebral injury on the dedicated monitoring interface, which is convenient for medical staff to intuitively View and analyze, the operation is simpler.
  • Fig. 2 includes a first display area for displaying waveform monitoring information corresponding to craniocerebral injury parameters. It can be seen that the patient's RR, Temp (body temperature), Art (arterial pressure), ICP, etc. are displayed in the first display area Waveform monitoring information of craniocerebral injury parameters within 8 hours. Specifically, the waveform monitoring information of these craniocerebral injury parameters can be displayed in the form of a trend graph, that is, the change of the detection data of craniocerebral injury parameters with time can be seen .
  • the corresponding display information will also be automatically refreshed in the first display area.
  • the parameter waveform information displayed in the first display area is based on the same time coordinate system. As shown in FIG. 2, the time axis of each parameter waveform graph/trend graph is 8 hours, to ensure that each parameter waveform The graph/trend graph is based on the same time period, which is convenient for medical staff to analyze the current physical condition of the monitored object.
  • the dedicated monitoring interface for craniocerebral injury may further include a second display area, which may display historical data of the Glasgow Coma Scale (Glasgow Coma Scale (GCS) score, specifically, the GCS The score value at that time point is marked at the corresponding time point on the time axis of the score.
  • GCS Glasgow Coma Scale
  • the GCS score includes three aspects: open eye response, language response and limb movement. The sum of the scores in these three areas is the coma index, which is a medical index commonly used to assess the degree of coma in patients.
  • the highest score of the GCS score is 15 points, indicating clear consciousness; 12-14 points are mild consciousness disorders; 9-11 points are moderate consciousness disorders; 8 points or less are coma; the lower the score, the more severe the consciousness disorder.
  • the medical monitoring device can calculate the GCS score by its own system.
  • the medical monitoring device can also obtain the GCS score from other medical devices, which is not specifically limited here.
  • the dedicated monitoring interface for craniocerebral injury may further include a third display area, which may also display historical data of pupil measurement results, specifically, the corresponding time on the time axis of pupil measurement
  • the pupil measurement value (including left and right eyes) at this time point is marked at the point.
  • the pupil is the hollow in the center of the iris of the eye, which is commonly known as the "black eye kernel", and the diameter is 3 to 4 mm.
  • the pupil of the normal person is round and the two sides are equal in size. Observation of pupil changes is of great significance for understanding the diagnosis and first aid of some diseases, especially intracranial diseases, poisoning, and critically ill patients.
  • the main monitoring interface of the medical monitoring device shown in FIG. 3 also includes a medical order tool display area on the left side, and medical personnel can click on the "pupil” in the medical order tool display area. "Measurement” display box, and then input the pupil measurement results measured at different periods into the medical monitoring device, the medical monitoring device can save each pupil measurement result, and display the pupil measurement result in the third display area of the dedicated monitoring interface for craniocerebral injury Historical data.
  • the display of the pupil measurement results includes the binocular measurement results of the patient.
  • the “L” mark is the pupil measurement result of the patient’s left eye
  • the “R” mark is The result of the pupil measurement of the patient's right eye.
  • the dedicated monitoring interface for craniocerebral injury also displays an entry of an analysis or treatment tool related to the craniocerebral injury.
  • the entry of the analysis or treatment tool includes the entry of the GCS scoring tool, as shown in FIG. 2
  • the "GCS score" display box shown in the lower right corner of the first display area in the middle.
  • first display area, the second display area, and the third display area are independent display areas, and the positional relationship between the three display areas is not specifically limited in this solution.
  • the content displayed in these display areas is related to the brain injury, and can be used as a reference for medical personnel to judge the brain injury.
  • the operator can open the GCS scoring menu interface by selecting the "GCS scoring" display box.
  • the medical staff can enter the corresponding data on the GCS scoring menu interface according to the actual situation of the patient, and finally the system calculates the GCS score Total score.
  • the display area of the GCS score in the second display area will display the latest GCS score, and update the historical data of the GCS score.
  • the operator can select the desired analysis or treatment tool entry by clicking on the touch operation method, and can also select the required analysis or treatment tool entry by clicking the mouse. , The specific is not limited here.
  • the monitoring interface includes four different display frames for “basic vital signs”, “hemodynamics”, “infection”, and “craniocerebral injury”, each The display box corresponds to the corresponding parameter set.
  • the monitoring device can respond to the selected instruction input by the operator, determine a target parameter set from the multiple parameter sets, and display the dedicated monitoring interface corresponding to the target parameter set, for example, a medical monitoring device After receiving the selected instruction from the operator clicking on the "Craniocerebral Injury" display box on the monitoring interface, the dedicated monitoring interface for craniocerebral injury is displayed.
  • the operator can switch and display between the dedicated monitoring interfaces of each parameter set by touch and slide.
  • the dedicated monitoring interface for craniocerebral injury also includes a graphical touch button, which can be specifically shown in the “>” shaped display box on the right side of the first display area in FIG. 2, and the medical monitoring device can obtain the user Based on the switching instruction input by the graphical touch area, based on the switching instruction, the monitoring device may choose to display the display information corresponding to the monitoring data in the first time period or the second time period. For example, before the medical monitoring device receives the switching instruction, the data of each parameter in the craniocerebral injury parameter set within 8 hours as shown in FIG. 2 is displayed. After the user enters the switching instruction, the monitoring device displays the craniocerebral injury parameter within 24 hours. The data of each physiological sign in the collection. It can be understood that, based on the switching instruction, the area of the dedicated graphical display interface can be enlarged or reduced.
  • the graphical touch button also has an indication function, indicating to the user that the dedicated monitoring interface for craniocerebral injury can be expanded or hidden, and the user can perform a touch and slide operation on the dedicated monitoring interface for craniocerebral injury, and hide the cranial by sliding to the left
  • the operator can adjust the special monitoring interface for craniocerebral injury of the medical monitoring device according to his own needs, making the display mode of the medical monitoring device more flexible.
  • the special monitoring interface for craniocerebral injury of medical monitoring equipment is described in detail above.
  • the main monitoring interface of medical monitoring equipment is further described below in conjunction with FIG. 5.
  • the main monitoring interface of medical monitoring equipment is in addition to the brain
  • the injury-specific monitoring interface at least further includes a real-time monitoring data display interface, which may be specifically shown in the area on the right side of the brain injury-specific monitoring interface.
  • the medical monitoring equipment can acquire real-time monitoring data of at least one physiological sign parameter of the monitored object, and generate display information corresponding to at least one physiological sign parameter according to the acquired real-time monitoring data, and then display at least one of the real-time monitoring data display interface Display information corresponding to physiological sign parameters.
  • the display information of the real-time monitoring data display interface may have waveform display information and numerical display information, and the waveform display information may also include a physiological waveform signal analog waveform diagram and a physiological diagram parameter trend diagram.
  • the real-time monitoring data display interface can be displayed in parallel with the special monitoring interface for craniocerebral injury.
  • the special monitoring interface for craniocerebral injury can also be suspended and displayed on the real-time monitoring data display interface, which is not limited here.
  • the medical monitoring device may also switch the operating mode of the medical monitoring device in response to an operation instruction input by the operator.
  • the operating mode may include setting of display content and/or display layout of the main monitoring interface of the medical monitoring device Information, one or more of the setting information of the monitoring process of the monitoring object and the alarm setting information of the physiological sign parameters.
  • the medical monitoring equipment has an independent housing, and a sensor interface area is provided on the housing panel, in which multiple sensor interfaces are integrated to connect with various external physiological parameter sensor accessories 111, and the housing panel also includes a small LCD display Area, display 119, input interface circuit 122, power and battery management circuit 117, memory 118, pump valve drive circuit 121 and alarm circuit 120 (such as LED alarm area) and so on.
  • the parameter processing module is used for external communication and power interface for communicating with the host and taking power from the host.
  • the parameter processing module also supports an extrapolation parameter module, which can form a plug-in medical monitoring device host by inserting the parameter module as a part of the medical monitoring device, or can be connected to the host through a cable, and the extrapolation parameter module acts as an external medical monitoring device.
  • an extrapolation parameter module which can form a plug-in medical monitoring device host by inserting the parameter module as a part of the medical monitoring device, or can be connected to the host through a cable, and the extrapolation parameter module acts as an external medical monitoring device.
  • the internal circuit of the parameter processing module is placed in the housing, as shown in FIG. 6, and includes at least two signal acquisition circuits 112 corresponding to physiological parameters, a front-end signal processing circuit 113, and a processor 115.
  • the signal acquisition circuit 112 may be selected from electrocardiograms Circuits, breathing circuits, body temperature circuits, blood oxygen circuits, non-invasive blood pressure circuits, invasive blood pressure circuits, etc. These signal acquisition circuits 112 are electrically connected to the corresponding sensor interfaces for electrical connection to sensor accessories corresponding to different physiological parameters 111. Its output terminal is coupled to the front-end signal processor.
  • the communication port of the front-end signal processor is coupled to the processor.
  • the processor is electrically connected to the external communication and power interface through the power supply and battery management circuit 117.
  • the front-end signal processor completes the sampling and analog-to-digital conversion of the signal acquisition circuit output signal, and outputs the control signal to control the physiological signal measurement process. These parameters include but are not limited to : ECG, respiration, body temperature, blood oxygen, noninvasive blood pressure and invasive blood pressure parameters.
  • the front-end signal processor can be implemented by a single-chip microcomputer or other semiconductor devices, or by ASIC or FPGA.
  • the front-end signal processor can be powered by an isolated power supply, and the sampled data can be sent to the processor through an isolated communication interface after simple processing and packaging.
  • the front-end signal processor circuit can be coupled to the processor 115 through the isolated power supply and the communication interface 114.
  • the reason why the front-end signal processor is powered by the isolated power supply is that the DC/DC power supply isolated by the transformer plays the role of isolating the patient from the power supply equipment.
  • the main purposes are: 1. Isolating the patient, floating the application part through the isolation transformer, so that The patient leakage current is small enough; 2. Prevent the voltage or energy during the application of defibrillation or electrocautery from affecting the cards and devices of the intermediate circuit such as the main control board (guaranteed by creepage distance and electrical clearance).
  • the processor completes the calculation of physiological parameters, and sends the calculation results and waveforms of the parameters to the host (such as a host with a display, a PC, a central station, etc.) through external communication and power interface.
  • the external communication and power interface 116 can be Ethernet One or a combination of a LAN (Ethernet), Token Ring (Token Ring), Token Bus (Token Bus), and the backbone network optical fiber distributed data interface (FDDI) as these three networks, or a combination thereof
  • LAN Local Area Network
  • Token Ring Token Ring
  • Token Bus Token Bus
  • FDDI backbone network optical fiber distributed data interface
  • wireless interfaces such as infrared, Bluetooth, wifi, and WMTS communication
  • wired data connection interfaces such as RS232 and USB.
  • the external communication and power supply interface 116 may also be one or a combination of two of a wireless data transmission interface and a wired data transmission interface.
  • the host can be any computer equipment such as a host of medical monitoring equipment, an electrocardiogram machine, an ultrasound diagnostic apparatus, a computer, etc., and installing the matched software can form a monitoring equipment.
  • the host can also be a communication device, such as a mobile phone, and the parameter processing module sends data to a mobile phone that supports Bluetooth communication through a Bluetooth interface to realize remote transmission of data.
  • the display 119 is used to configure the display information according to the instructions of the processor 115;
  • the processor 115 executes program instructions to implement the following steps:
  • physiological signs related to the craniocerebral injury of the monitored object where the physiological signs related to the craniocerebral injury include at least blood pressure and body temperature;
  • a dedicated monitoring interface for craniocerebral injury Displaying a dedicated monitoring interface for craniocerebral injury, wherein the dedicated monitoring interface for craniocerebral injury includes at least a first display area;
  • the waveform monitoring information corresponding to the physiological signs related to the craniocerebral injury is displayed on the first display area.
  • the monitoring device in addition to displaying the waveform information of each basic vital sign parameter, can also display the data of the craniocerebral injury parameter in the first display area of the monitoring interface of the monitoring device, which is convenient for the medical staff to view and Analysis, the operation is simpler.
  • the physiological signs related to the craniocerebral injury further include one or more of respiration rate, intracranial pressure, and EEG dual frequency index.
  • the processor 115 is configured to:
  • the plurality of parameter sets being determined and obtained according to the correlation of the physiological signs of the monitored object, the plurality of parameter sets including the parameter sets of the physiological signs related to the craniocerebral injury;
  • a dedicated display interface corresponding to the target parameter set is generated, and the waveform monitoring information of the physiological signs corresponding to the target parameter set is displayed in the dedicated display interface.
  • the dedicated monitoring interface for craniocerebral injury further includes a second display area
  • the processor 115 is configured to:
  • the Glasgow coma score of the monitored subject is obtained, and the Glasgow coma score is displayed in the second display area.
  • the dedicated monitoring interface for craniocerebral injury further includes a third display area, and the processor 115 is configured to:
  • the processor 115 is configured to:
  • an entry of an analysis or treatment tool related to the craniocerebral injury is displayed, and the entry of the analysis or treatment tool includes at least the entry of the scoring tool of the Glasgow coma scoring method.
  • the processor 115 is configured to:
  • the switching instruction it is determined to display the waveform monitoring information corresponding to the physiological signs related to the craniocerebral injury in the first time period, or to display the waveform monitoring information corresponding to the physiological signs related to the craniocerebral injury in the second time period.
  • the processor 115 is configured to:
  • the real-time monitoring data is displayed in other display areas of the main monitoring interface except the dedicated monitoring interface for craniocerebral injury.
  • the disclosed system, device, and method may be implemented in other ways.
  • the device embodiments described above are only schematic.
  • the division of the units is only a logical function division, and there may be other divisions in actual implementation, for example, multiple units or components may be combined or Can be integrated into another system, or some features can be ignored, or not implemented.
  • the displayed or discussed mutual coupling or direct coupling or communication connection may be indirect coupling or communication connection through some interfaces, devices or units, and may be in electrical, mechanical, or other forms.
  • the units described as separate components may or may not be physically separated, and the components displayed as units may or may not be physical units, that is, they may be located in one place, or may be distributed on multiple network units. Some or all of the units may be selected according to actual needs to achieve the purpose of the solution of this embodiment.
  • each functional unit in each embodiment of the present invention may be integrated into one processing unit, or each unit may exist alone physically, or two or more units may be integrated into one unit.
  • the above integrated unit can be implemented in the form of hardware or software function unit.
  • the integrated unit is implemented in the form of a software functional unit and sold or used as an independent product, it may be stored in a computer-readable storage medium.
  • the technical solution of the present invention essentially or part of the contribution to the existing technology or all or part of the technical solution can be embodied in the form of a software product
  • the computer software product is stored in a storage medium It includes several instructions to enable a computer device (which may be a personal computer, server, or network device, etc.) to perform all or part of the steps of the methods described in various embodiments of the present invention.
  • the aforementioned storage media include: U disk, mobile hard disk, read-only memory (ROM), random access memory (RAM), magnetic disk or optical disk and other media that can store program codes .

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Abstract

L'invention concerne un procédé de surveillance de signe physiologique pour une lésion cranio-cérébrale et un dispositif de surveillance médicale. Le procédé consiste à : obtenir des signes physiologiques liés à une lésion cranio-cérébrale d'un objet surveillé, les signes physiologiques liés à la lésion cranio-cérébrale comprenant au moins la tension artérielle et la température corporelle ; obtenir des données de surveillance correspondant aux signes physiologiques liés à la lésion cranio-cérébrale ; sur la base des données de surveillance correspondant aux signes physiologiques liés à la lésion cranio-cérébrale, générer des informations de surveillance de forme d'onde correspondant aux signes physiologiques liés à la lésion cranio-cérébrale ; afficher une interface spéciale de surveillance de lésion cranio-cérébrale, l'interface spéciale de surveillance de lésion cranio-cérébrale comprenant au moins une première zone d'affichage ; et afficher, dans la première zone d'affichage, les informations de surveillance de forme d'onde correspondant aux signes physiologiques liés à la lésion cranio-cérébrale.
PCT/CN2018/123122 2018-12-24 2018-12-24 Procédé de surveillance de signe physiologique pour lésion cranio-cérébrale et dispositif de surveillance médicale Ceased WO2020132813A1 (fr)

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Application Number Priority Date Filing Date Title
PCT/CN2018/123122 WO2020132813A1 (fr) 2018-12-24 2018-12-24 Procédé de surveillance de signe physiologique pour lésion cranio-cérébrale et dispositif de surveillance médicale
CN201880098526.4A CN112839564B (zh) 2018-12-24 2018-12-24 针对颅脑损伤的生理体征监测方法和医疗监护设备

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PCT/CN2018/123122 WO2020132813A1 (fr) 2018-12-24 2018-12-24 Procédé de surveillance de signe physiologique pour lésion cranio-cérébrale et dispositif de surveillance médicale

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CN116634931A (zh) * 2020-12-25 2023-08-22 深圳迈瑞生物医疗电子股份有限公司 监护设备和用于监护设备的显示方法
CN116669618A (zh) * 2020-12-25 2023-08-29 深圳迈瑞生物医疗电子股份有限公司 监护设备和用于监护设备的显示方法

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WO2023006116A1 (fr) * 2021-07-30 2023-02-02 深圳迈瑞生物医疗电子股份有限公司 Dispositif de surveillance et procédé d'affichage pour objet cible
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