Medical equipment, display processing method thereof and storage medium

Abstract

The invention provides medical equipment, a display processing method thereof and a storage medium. The method comprises the following steps: acquiring first clinical information and second clinical information of a patient; displaying the first clinical information in a first display area of a display interface, and displaying the second clinical information in a second display area of the display interface; receiving a first selection operation input by a user to determine a first moment; acquiring first information which corresponds to the first clinical information and is associated with a first moment, and acquiring second information which corresponds to the second clinical information and is associated with the first moment; and displaying the first information and the second information in the display interface in a set mode. Through the method, the working efficiency of the user can be improved.

Description

Medical device, display processing method, and storage medium thereof Technical Field

[0001] The present invention relates to the field of medical technology, and in particular to a medical device, and a display processing method and storage medium of the medical device. Background Art

[0002] With the advancement of clinical monitoring technology and improved diagnostic and treatment methods in the medical field, the demand for data reflecting patient status and symptoms is increasing. However, this increasing abundance of clinical parameter data also presents new challenges for medical staff. Medical staff must search and aggregate data from various devices and systems to fully assess a patient's condition (e.g., integrating patient monitors, ventilators, biochemical test results, and hospital imaging results). They must also identify key data within this massive data set for clinical analysis and treatment (e.g., identifying abnormalities in a patient's monitoring data over the past 24 hours, or identifying key indicators that reflect changes in a patient's condition over the past week). Both the aggregation of large amounts of clinical data from multiple sources and the search for clues to clinical diagnosis and treatment within this vast data set consume significant time and effort, reducing diagnostic and treatment efficiency. In particular, medical staff are particularly concerned with clinical parameters before and after critical moments. For example, after medication administration, medical staff need to review vital sign data before and after administration to assess its effectiveness. Current medical equipment requires medical staff to search for this data themselves, which is cumbersome and inefficient. Technical issues

[0003] The technical problem to be solved by this application is to provide a medical device and a display processing method thereof that facilitates users to view different types of clinical information at the same time, or facilitates users to view the same type of clinical information at different times. Technical Solutions

[0004] According to a first aspect, an embodiment provides a display processing method for a medical device, comprising:

[0005] obtaining first clinical information and second clinical information of the patient;

[0006] Displaying the first clinical information in a first display area of ​​the display interface and displaying the second clinical information in a second display area of ​​the display interface;

[0007] receiving a first selection operation input by a user to determine a first moment;

[0008] Acquire first information associated with a first moment corresponding to the first clinical information, and acquire second information associated with the first moment corresponding to the second clinical information;

[0009] The first information and the second information are displayed in a set manner on the display interface.

[0010] According to a second aspect, an embodiment provides a display processing method for a medical device, comprising:

[0011] Obtain the patient's first clinical information;

[0012] Displaying the first clinical information on a display interface;

[0013] receiving a first selection operation input by a user to determine a first time, and receiving a second selection operation input to determine a second time different from the first time;

[0014] Acquire first information associated with a first moment and corresponding third information associated with a second moment, corresponding to the first clinical information;

[0015] The first information and the third information corresponding to the first clinical information are compared and displayed in the display interface.

[0016] According to a third aspect, an embodiment provides a medical device, comprising:

[0017] Memory, used to store programs;

[0018] A processor is configured to implement the methods of the first and second aspects by executing the program stored in the memory.

[0019] According to a fourth aspect, an embodiment provides a computer-readable storage medium, on which a program is stored. The program can be executed by a processor to implement the methods of the first and second aspects above. Beneficial effects

[0020] According to the medical equipment and display processing method thereof in some of the above-mentioned embodiments, the first clinical information is displayed in the first display area, and the second clinical information is displayed in the second display area. When the user selects the first moment, the first information associated with the first moment in the first clinical information is displayed in a set manner in the display interface, and the second information associated with the first moment in the second clinical information is displayed in a set manner. Therefore, the user can intuitively view the information associated with the first moment corresponding to the two types of clinical information, thereby reducing the workload of searching for data and greatly improving the user's work efficiency.

[0021] According to the medical equipment and display processing method thereof of some other embodiments mentioned above, the first clinical information is displayed in the display interface. When the user selects the first moment and the second moment, the first information associated with the first moment and the third information associated with the second moment in the first clinical information are compared and displayed in the display interface. In this way, the user can easily compare the information associated with different moments in the first clinical information, which also improves the user's work efficiency. BRIEF DESCRIPTION OF THE DRAWINGS

[0022] FIG1 is a structural block diagram of a medical device according to an embodiment;

[0023] FIG2 is a flow chart of a display processing method according to an embodiment;

[0024] FIG3 is a schematic diagram of a display interface according to an embodiment;

[0025] FIG4 is a schematic diagram of a display interface according to another embodiment;

[0026] FIG5 is a schematic diagram of a display interface according to another embodiment;

[0027] FIG6 is a schematic diagram of a display interface according to another embodiment;

[0028] FIG7 is a schematic diagram of a display interface according to another embodiment;

[0029] FIG8 is a schematic diagram of a display interface according to another embodiment;

[0030] FIG9 is a schematic diagram of a display interface according to another embodiment;

[0031] FIG10 is a schematic diagram of a display interface of a circulation system according to an embodiment;

[0032] FIG11 is a schematic diagram of a display interface of a respiratory system according to an embodiment;

[0033] FIG12 is a schematic diagram of a display interface of a nervous system according to an embodiment;

[0034] FIG13 is a schematic diagram of a first display area according to an embodiment;

[0035] FIG14 is a schematic diagram of a first display area according to another embodiment;

[0036] FIG15 is a schematic diagram showing a second window created in a first display area according to an embodiment;

[0037] FIG. 16 is a schematic diagram showing a fourth window created in the first display area according to an embodiment.

[0038] FIG17 is a schematic diagram of a target management area according to an embodiment;

[0039] FIG18 is a schematic diagram of a target management area according to another embodiment;

[0040] FIG19 is a flowchart of a display processing method according to another embodiment;

[0041] FIG20 is a schematic diagram of a display interface according to yet another embodiment;

[0042] FIG21 is a schematic diagram of a display interface according to yet another embodiment. Modes for Carrying Out the Invention

[0043] The present invention will be further described in detail below by means of specific embodiments in conjunction with the accompanying drawings. Similar elements in different embodiments are numbered with associated similar elements. In the following embodiments, many detailed descriptions are provided to enable the present application to be better understood. However, those skilled in the art will readily appreciate that some of the features may be omitted in different circumstances, or may be replaced by other elements, materials, or methods. In some cases, some operations related to the present application are not shown or described in the specification. This is to avoid the core portion of the present application being overwhelmed by excessive descriptions, and for those skilled in the art, it is not necessary to describe these related operations in detail. They will fully understand the related operations based on the description in the specification and the general technical knowledge in the art.

[0044] In addition, the features, operations, or characteristics described in the specification may be combined in any appropriate manner to form various embodiments. Furthermore, the steps or actions in the method description may be reordered or adjusted in a manner readily apparent to those skilled in the art. Therefore, the various sequences in the specification and drawings are provided solely for the purpose of clearly describing a particular embodiment and are not intended to be mandatory, unless otherwise specified.

[0045] Component numbers used herein, such as "first" and "second," are used solely to distinguish the components being described and do not convey any sequential or technical meaning. References to "connection" and "coupling" herein, unless otherwise specified, include both direct and indirect connections (couplings).

[0046] In some embodiments of the present application, the first clinical information and the second clinical information are associated with the same physiological structure. Hereinafter, the physiological structure associated with both the first clinical information and the second clinical information is defined as a target physiological structure. The physiological structure referred to in the present application is a patient's physiological system, physiological organ, physiological part, tissue, physiological system characteristic, or physiological organ characteristic, wherein the physiological system includes at least one of the locomotor system, nervous system, endocrine system, circulatory system, respiratory system, digestive system, urinary system, and reproductive system; the physiological organ includes at least one of the brain, heart, lung, liver, stomach, and kidney; the physiological part includes at least one of the head, chest, and abdomen; the tissue includes at least one of muscle tissue, nervous tissue, and epithelial tissue; and the characteristic of the physiological system or the characteristic of the physiological organ includes coagulation, nutrition, infection, or blood sugar.

[0047] In some embodiments, the first clinical information and the second clinical information are determined based on clinical parameters associated with the target physiological structure. For example, if the target physiological structure is a patient's respiratory system, the first clinical information may be the historical trends of important physiological parameters in the patient's respiratory system, and the second clinical information may be abnormal events occurring in the patient's respiratory system, with the abnormal events being determined based on the clinical parameters associated with the respiratory system. The following examples illustrate clinical parameters associated with various physiological structures.

[0048] Clinical parameters related to the respiratory system include but are not limited to oxygenation index (PaO2 / FiO2), blood oxygen saturation (SpO2), respiratory rate (RR), inspired oxygen concentration (FiO2), end-tidal carbon dioxide, blood gas analysis parameters and / or ventilator parameters, among which blood gas analysis parameters include lactate (Lac), arterial oxygen partial pressure (PaO2), arterial carbon dioxide partial pressure (PaCO2), etc.; ventilator parameters include tidal volume (Tv), positive end-expiratory pressure (PEEP), and the current patient oxygen supply mode, for example, whether to use SIMV ventilation mode, intubation or mask oxygen supply, etc.

[0049] Clinical parameters related to the circulatory system include but are not limited to shock index, blood pressure, cardiac output, lactate (Lac), laboratory indicators related to hemodynamics and perfusion, and hemodynamic parameters. Blood pressure can be invasive or non-invasive, and laboratory indicators include but are not limited to hemoglobin (Hb or HGB), red blood cell count (RBC), pH, HCO3, and base excess (BE). Hemodynamic parameters include but are not limited to central venous pressure (CVP), peripheral vascular resistance index (SVRI), lung water index (ELWI), and central venous oxygen saturation (ScvO2).

[0050] Neurological clinical parameters include, but are not limited to, consciousness score, cerebral blood pressure, blood oxygen levels, and other neurological clinical assessment results. The Glasgow Coma Scale (GCS) is the most commonly used consciousness score in clinical practice, but users can also define their own consciousness scoring rules. Neurological clinical assessment results include, but are not limited to, pupil size assessment, pupil light reflex assessment, and limb muscle strength assessment.

[0051] Cardiac-related clinical parameters include cardiac risk assessment results, heart rate, and cardiac biochemical markers. Examples of cardiac risk assessment results include the TIMI (Thrombolysis in Myocardial Infarction) score. If the patient underwent a GRACE (Global Registry for Acute Coronary Syndromes) assessment, the cardiac risk assessment results may also include the GRACE score. Examples of cardiac biochemical markers include creatine kinase-MB (CK-MB), troponin (cTn), and natriuretic peptide (NT-proBNP).

[0052] Liver-related clinical parameters include but are not limited to liver function assessment indicators. The default liver function assessment indicators include alanine aminotransferase (ALT), gamma-glutamyl transaminase (GGT), total bilirubin (Tbil), direct bilirubin (Dbil), and blood ammonia (AMM).

[0053] Kidney-related clinical parameters include, but are not limited to, creatinine levels and fluid intake and output. Fluid intake includes total 24-hour intake and the amount of fluid pumped into the body via an infusion pump within 24 hours. Fluid intake can also include dietary fluids. Fluid output includes 24-hour urine output, 24-hour drainage volume, and fluid dehydration from other devices. Fluid output can also include the amount of fluid produced through sweating, excretion, vomiting, and bleeding.

[0054] Infection-related clinical parameters include infection-related biochemical index parameters and infection-related vital sign parameters. Infection-related biochemical index parameters 503 include, but are not limited to, white blood cell count (WBC), C-reactive protein (CRP), procalcitonin (PCT), interleukin-6 (IL-6), and neutrophil percentage (NEU%); infection-related vital sign parameters include, but are not limited to, body temperature.

[0055] Coagulation-related clinical parameters include, but are not limited to, coagulation risk assessment results, coagulation indices, and bleeding indices. For surgical patients, the Caprini scale can be used for coagulation risk assessment, while for non-surgical patients, the Padua scale can be used. Coagulation indices 1202 include at least one of the following: activated partial thromboplastin time (APTT), thrombin time (TT), fibrinogen (Fib), D-dimer (D-dimer), fibrin degradation products (FDP), and antithrombin III (AT-III). Bleeding indices include platelets (PLT) and occult blood (OB).

[0056] Nutrition-related clinical parameters include, but are not limited to, energy metabolism monitoring results, trace element supply, and feeding methods. Energy metabolism monitoring results include energy metabolism value (EE) and its changing trend. Trace elements mainly include calcium, iron, potassium, sodium, magnesium, etc. Feeding methods mainly include parenteral nutrition and enteral nutrition. Parenteral nutrition can be further divided into deep vein nutrition and superficial vein nutrition; enteral nutrition can be further divided into nasogastric feeding and gastric tube feeding.

[0057] In some embodiments of the present application, the first clinical information and the second clinical information are divided based on different correlations. That is, the information, parameters, etc. in the first clinical information have a certain correlation, and the information, parameters, etc. in the second clinical information also have a certain correlation. For example, if two types of parameters in the first clinical information can both reflect a certain state of the physiological structure, then the two parameters are correlated.

[0058] In some embodiments, the above-mentioned correlation is divided based on preset rules. For example, the correlation between different parameters / information can be determined based on at least one of the source device, function and usage scenario of the parameter / information. For example, the parameter / information obtained by device A belongs to the first clinical information, and the parameter / information obtained by device B belongs to the second clinical information.

[0059] In some embodiments, the first clinical information and the second clinical information can be determined based on the user's selection. In other embodiments, it can also be determined based on a preset machine learning algorithm which parameters / information belong to the first clinical information and which parameters / information belong to the second clinical information.

[0060] The medical devices referred to in this application include but are not limited to central stations, monitors, etc. In one embodiment of this application, FIG1 shows the hardware and / or software architecture of a central station 100 in one embodiment.

[0061] The central station 100 includes a processor 110 (which may be composed of one or more processors and / or controllers), a memory 120 (which may include one or more computer-readable storage media), an I / O subsystem 130, a display system 140, a peripheral interface 150, and other input devices.

[0062] The display system 140 may include at least one display screen. In some embodiments, the display screen is non-touch, and the user can input commands through peripherals connected to the peripheral interface 150. Peripherals include, but are not limited to, a mouse, keyboard, gesture recognition device, and other devices.

[0063] In some embodiments, the display screen may include a stacked touch layer and a display layer. The touch layer provides an input / output interface between the central station 100 and the user. The touch layer may be composed of a resistive screen, a surface acoustic wave screen, an infrared touch screen, an optical touch screen, a capacitive screen, or a nanofilm, and is an inductive display device that can receive input signals such as a touch probe. Visual output may optionally include graphics, text, charts, videos, or combinations thereof. Some or all of the visual output may correspond to user interface objects.

[0064] The display screen can also receive user input based on touch and / or contact. The touch layer of the display screen forms a touch-sensitive surface that receives user input. The touch layer and display controller detect contact (and any movement or interruption of the touch) on the touch layer and convert the detected contact into interaction with a user interface object, such as one or more soft keys, displayed on the touch layer. In an exemplary embodiment, the point of contact between the touch layer and the user corresponds to one or more fingers of the user. The touch layer can use LCD (liquid crystal display) technology or LPD (light emitting polymer display) technology, but other display technologies can be used in other embodiments. The touch layer and display controller can use any of a variety of touch-sensitive technologies to detect contact and its movement or interruption, including but not limited to capacitive, resistive, infrared and surface acoustic wave technologies, as well as other proximity sensor arrays, or other technologies for determining one or more points of contact with the touch layer.

[0065] In some embodiments, the display system 140 includes more than two display screens.

[0066] Of course, the central station 100 may also include a communication module 160, an audio processor 170, a speaker 180, and a power supply system 190 (including a DC / DC conversion circuit and / or an AC / DC conversion circuit).

[0067] The memory 120 may include high-speed random access memory and may also include non-volatile memory, such as one or more magnetic disk storage devices, flash memory devices, or other non-volatile solid-state storage devices. In some embodiments, the memory 120 may also include a memory 120 that is remote from the one or more processors 110, such as a network attached storage accessed via the communication module 160 and a communication network (not shown), wherein the communication network may be the Internet, one or more intranets, a local area network (LAN), a wide area network (WAN), a storage area network (SAN), or the like, or a suitable combination thereof.

[0068] Peripheral interface 150 couples the input and output peripherals of central station 100 with processor 110. Processor 110 runs or executes various software programs and / or instruction sets stored in memory 120 to perform various functions and applications of the device and process data.

[0069] In various embodiments of the present invention, the peripheral interface 150, the processor 110 (CPU), and the memory 120 may be implemented on, for example, a single chip. In some embodiments, they may also be implemented on multiple separate chips. The processor 110, together with the peripheral interface 150, the memory 120, or a portion thereof, constitutes a processing unit.

[0070] The communication module 160 is used to receive communication signals and convert them into electrical signals, and to convert electrical signals into communication signals for transmission. The communication module 160 can be implemented using any method known in the art, primarily to enable the central station 100 to communicate with an external network or other external devices. For example, the communication module 160 can access the World Wide Web (WWW) Internet, an intranet, and / or wireless and / or wired networks such as cellular telephone networks, local area networks (LANs), and / or metropolitan area networks (MANs), as well as other devices. The communication module 160 can utilize any of a variety of communication standards, protocols, and technologies, including but not limited to wired or wireless media, including those based on Bluetooth, Ethernet, 802.11(x), body area networks, or other wireless protocols.

[0071] The audio processor 170 may receive audio data from the peripheral interface 150, convert the audio data into an electrical signal, and transmit the electrical signal to the speaker 180. The speaker 180 converts the electrical signal into sound waves audible to humans.

[0072] The I / O subsystem 130 couples the display system 140 and other input devices to the peripheral interface 150. The I / O subsystem 130 may include a display controller and one or more other input controllers for controlling other input devices. The one or more other input controllers receive and send electrical signals to other input devices. Other input devices may include physical buttons and similar devices.

[0073] The central station 100 also includes a power system 190 that provides power input to various components, modules, or circuits. The power system 190 includes a power management system, one or more power sources (e.g., batteries, alternating current (AC)), a charging system, a power fault detection circuit, a power converter or inverter, a power status indicator (e.g., a light-emitting diode (LED)), and any other components related to the generation, management, and distribution of power in the central station 100. Depending on the power source, it may include a DC / DC conversion circuit or an AC / DC conversion circuit.

[0074] FIG1 merely provides a block diagram of the structure of a central station 100. Of course, the central station 100 may include more or fewer elements or modules than those shown in FIG1 , may combine two or more elements or modules, or may have different configurations of the architecture shown in FIG1 . The various elements or modules shown in FIG1 may be implemented in hardware, software, or a combination of hardware and software, including one or more signal processing and / or application-specific integrated circuits.

[0075] Based on the above medical device, as shown in FIG2 , an embodiment of the present application provides a display processing method, including:

[0076] Step A100: Acquire first clinical information and second clinical information of the patient.

[0077] The clinical information in this step refers to clinically relevant information, including but not limited to monitoring information, infusion information, and alarm information. Clinical information can be collected and acquired through sensors on the medical device itself, third-party devices, application software, or user input.

[0078] In some embodiments, the first clinical information and the second clinical information are different, and the difference here includes at least three situations.

[0079] 1. The first clinical information and the second clinical information are completely different. For example, the first clinical information is monitoring information, and the second clinical information is alarm information. For another example, the clinical information from device A is the first clinical information, and the information from device B is the second clinical information.

[0080] 2. The first clinical information and the second clinical information partially overlap. For example, the first clinical information is related to the respiratory system, and the second clinical information is related to the circulatory system. If the patient's physiological parameter trend graph is related to both the respiratory and circulatory systems, then the information related to the physiological parameter trend graph belongs to both the first and second clinical information.

[0081] 3. One of the first clinical information and the second clinical information includes the other, for example, the first clinical information completely includes the second clinical information.

[0082] Step A200: Display first clinical information in the first display area 10a of the display interface, and display second clinical information in the second display area 10b of the display interface.

[0083] The present application does not limit the shape, area, and size of the first display area 10a and the second display area 10b. For example, the first display area 10a and the second display area 10b can be arranged side by side, and the second display area 10b can also be embedded in the first display area 10a.

[0084] In some embodiments, if the first clinical information includes trend graph-type information, the corresponding first information includes parameter data associated with the trend graph at the first moment. As shown in FIG3 , the first clinical information includes a trend graph of a first type of parameter, and the second clinical information includes a trend graph of a second type of parameter. In other words, the first clinical information can reflect the historical trend of the first type of parameter, and the second clinical information can reflect the historical trend of the second type of parameter. The first type of parameter and the second type of parameter can be the same or different. For example, the first type of parameter is the patient's heart rate, and the second type of parameter is an ultrasound parameter obtained by performing an ultrasound examination on the patient. According to the type of trend graph, the trend graph of the first category parameters and the trend graph of the second category parameters may include but are not limited to a curve graph, a broken line graph, etc. For example, the trend graph of the first category parameters and the trend graph of the second category parameters are both curve graphs. For another example, the trend graph of the first category parameters is a curve graph, and the trend graph of the second category parameters is a broken line graph. According to the type of parameter data, the trend graph also has different forms. In some embodiments, the parameter data of the first category parameters is continuous data, and the trend graph of the first category parameters is a continuous trend graph. In other embodiments, the parameter data of the first category parameters is discrete data, and the trend graph of the first category parameters is a discrete trend graph. In contrast, when the parameter data of the second category parameters is continuous data, the trend graph of the second category parameters is a continuous trend graph. When the parameter data of the second category parameters is discrete data, the trend graph of the second category parameters is a discrete trend graph.

[0085] In the present application, the time axis of the trend graph of the first type of parameter is defined as a first time axis 20a, and the time axis of the trend graph of the second type of parameter is defined as a second time axis 20b. In some embodiments, the first time axis 20a is different from the second time axis 20b. In this case, the first time axis 20a and the second time axis 20b are different in at least the following situations:

[0086] First, the time period represented by the first time axis 20a is different from the time period represented by the second time axis 20b. Similar to the difference between the first clinical information and the second clinical information: in some embodiments, the time period represented by the first time axis 20a does not overlap with the time period represented by the second time axis 20b, for example, the first time axis 20a represents the time period from the past 24 hours to the past 12 hours, and the second time axis 20b represents the time period from the past 12 hours to the present; in some embodiments, the time period represented by the first time axis 20a overlaps with the time period represented by the second time axis 20b, for example, the first time axis 20a represents the time period from the past 24 hours to the past 8 hours, and the second time axis 20b represents the time period from the past 12 hours to the present; in other embodiments, one of the time periods represented by the first time axis 20a and the time period represented by the second time axis 20b includes the other, for example, the first time axis 20a represents the time period from the past 24 hours to the present, and the second time axis 20b represents the time period from the past 12 hours to the present.

[0087] Second, the duration represented by the unit scale on the first time axis 20a is different from the duration represented by the unit scale on the second time axis 20b. For example, the duration represented by each unit scale on the first time axis 20a is 1s, and the duration represented by each unit scale on the second time axis 20b is 5s.

[0088] In some embodiments, the first and second situations mentioned above can occur simultaneously. For example, the first time axis 20a represents the time period from the past 12 hours to the present, and the second time axis 20b represents the time period from the past 24 hours to the present. The duration represented by each unit scale on the first time axis 20a is 1s, and the duration represented by each unit scale on the second time axis 20b is 2s. Then the lengths of the first time axis 20a and the second time axis 20b are the same.

[0089] In some embodiments, when the first clinical information includes trend graphs of multiple first-category parameters, the trend graphs of multiple first-category parameters can share the same first time axis 20a, for example, the trend graphs of multiple first-category parameters are arranged side by side above the first time axis 20a, that is, multiple information of the same type share the same time axis; in some embodiments, when the second clinical information includes trend graphs of multiple second-category parameters, the trend graphs of multiple second-category parameters can share the same second time axis 20b, for example, the trend graphs of multiple second-category parameters are arranged side by side above the second time axis 20b.

[0090] The first time axis 20a can be displayed in the first display area 10a or can be hidden. Similarly, the second time axis 20b can be displayed in the second display area 10b or can be hidden.

[0091] In some embodiments, as shown in FIG4 and FIG5 , the first clinical information includes, in addition to a trend graph of the first type of parameter, markers 30 for events associated with the patient. Events herein include, but are not limited to, abnormal physiological state events, examination events, test events, and treatment events experienced by the patient. It is understood that these events are also related to time. For example, if the patient's physiological state is abnormal at time A, then time A is defined as the time when the abnormal physiological state event occurs. For another example, if an ultrasound examination is performed on the patient at time B and ultrasound image data is obtained, then at time B the patient experienced an examination event. For another example, if a routine blood test is performed on the patient's blood sample at time C and a routine blood test result is obtained, then at time C the patient experienced a test event. For another example, if a therapeutic drug is infused into the patient at time D, then at time D the patient experienced a treatment event. In some embodiments, markers 30 for different types of events are displayed differently. For example, markers 30 for abnormal physiological state events are red, and markers 30 for test events are blue.

[0092] As can be seen from the above description, the aforementioned events and time are also related, and the event markers 30 can also be sorted according to chronological order. In some embodiments, as shown in FIG5 , the event markers 30 in the first display area 10a can be distributed along the first time axis 20a, that is, multiple information of different types also share the same time axis. When there are multiple event markers 30, the event markers 30 can form event bars along the first time axis 20a. In some embodiments, the event markers 30 of different types form different event bars. For example, the markers 30 for abnormal physiological state events form one event bar parallel to the first time axis 20a, while the markers 30 for examination events form another event bar parallel to the first time axis 20a.

[0093] In some embodiments, the second clinical information includes, in addition to a trend graph of the second type of parameter, markers 30 for events associated with the patient. These events include, but are not limited to, abnormal physiological state events, examination events, test events, and treatment events experienced by the patient. Similar to the first clinical information including markers 30 for events associated with the patient, the markers 30 for events in the second display area 10b can be distributed along the second time axis 20b. When there are multiple markers 30 for an event, the markers 30 can form event bars along the second time axis 20b. In some embodiments, markers 30 for different types of events form different event bars. For example, markers 30 for abnormal physiological state events form one event bar parallel to the second time axis 20b, while markers 30 for examination events form another event bar parallel to the second time axis 20b.

[0094] In some embodiments, as shown in Figure 6, the first clinical information includes a trend graph of the first category of parameters but does not include a mark 30 of the event, and the second clinical information includes a mark 30 of the event but does not include a trend graph of the second category of parameters, or, the first clinical information includes a mark 30 of the event but does not include a trend graph of the first category of parameters, and the second clinical information includes a trend graph of the second category of parameters but does not include a mark 30 of the event, that is, the first display area 10a and the second display area 10b, one displays a trend graph of the parameters, and the other displays a mark 30 of the event.

[0095] In some embodiments, as shown in FIG. 7 , both the first clinical information and the second clinical information include event marks 30 , that is, both the first display area 10 a and the second display area 10 b display event marks 30 .

[0096] Step A300: Receive a first selection operation input by the user to determine a first moment.

[0097] In some embodiments, the first selected operation is an operation performed by the user in the first display area 10a. Based on the above description of the first clinical information, the first selected operation input by the user includes at least the following methods:

[0098] When the first clinical information includes a trend graph of a first type of parameter, in some embodiments, the first display area 10a includes an area for the user to select a point. When the user selects any point in the area, the first moment can be determined based on the corresponding position of the point on the first time axis 20a; in other embodiments, when the trend graph of the first type of parameter is a continuous trend graph, the user can select any point on the trend graph, and the first moment can be determined based on the corresponding position of the point on the first time axis 20a; when the trend graph of the first type of parameter is a discrete trend graph, the user can first select a discrete point on the trend graph, and then determine the first moment based on the position of the discrete point on the first time axis 20a.

[0099] When the first clinical information includes a trend graph of a first-category parameter, in some embodiments, as shown in FIG3 , the first display area 10a further includes a first reference cursor 40a that is movable along the first time axis 20a. For example, in conjunction with the above description, after a user clicks any point, the first reference cursor 40a is moved to or changed to display the first moment corresponding to that point. In another example, the user can determine the first moment by dragging the first reference cursor 40a. For example, the user can drag the first reference cursor 40a to a certain position along the first time axis 20a and then enter a confirmation command. The first moment can then be determined based on the position of the first reference cursor 40a on the first time axis 20a.

[0100] When the first clinical information includes event marks 30, in some embodiments, the user can determine the first moment by selecting any mark 30. For example, if the user selects an abnormal physiological state event, the abnormal physiological state event will be used as the first moment.

[0101] In some embodiments, the first selected operation is an operation performed by the user in the second display area 10b. Based on the above description of the second clinical information, the first selected operation input by the user includes at least the following methods:

[0102] When the second clinical information includes a trend graph of the second category of parameters, in some embodiments, the second display area 10b includes an area for the user to select a point. When the user selects any point in the area, the first moment can be determined based on the corresponding position of the point on the second time axis 20b; in other embodiments, when the trend graph of the second category of parameters is a continuous trend graph, the user can select any point on the trend graph, and the first moment can be determined based on the corresponding position of the point on the second time axis 20b; when the trend graph of the second category of parameters is a discrete trend graph, the user can first select a discrete point on the trend graph, and then determine the first moment based on the position of the discrete point on the second time axis 20b.

[0103] When the second clinical information includes a trend graph of a second parameter, in some embodiments, the second display area 10b further includes a second reference cursor 40b that is movable along the second time axis 20b. For example, in conjunction with the above description, after a user clicks any point, the second reference cursor 40b is moved to or changed to display the first moment corresponding to that point. In another example, the user can determine the first moment by dragging the second reference cursor 40b. For example, the user can drag the second reference cursor 40b to a certain position along the second time axis 20b and then enter a confirmation command. The first moment is then determined based on the position of the second reference cursor 40b on the second time axis 20b.

[0104] When the second clinical information includes event marks 30, in some embodiments, the user can determine the first moment by selecting any mark 30. For example, if the user selects an abnormal physiological state event, the abnormal physiological state event will be used as the first moment.

[0105] In some embodiments, the display interface also includes a fourth display area 10d independent of the first display area 10a and the second display area 10b. The first selection operation is an operation performed by the user in the fourth display area 10d. That is, the user can determine the first moment related to the first clinical information and the second clinical information by inputting the selection operation in other display areas in the display interface.

[0106] Step A400: Acquire first information associated with the first moment corresponding to the first clinical information, and acquire second information associated with the first moment corresponding to the second clinical information.

[0107] When the first clinical information includes a trend graph of a first-category parameter, the first information includes first parameter data of the first-category parameter, where the first parameter data is parameter data of the first-category parameter associated with a first moment. In some embodiments, the first parameter data is parameter data of the first-category parameter at the first moment. It will be understood that if the first clinical information includes multiple trend graphs of first-category parameters, multiple first parameter data may be included.

[0108] In some embodiments, when the first clinical information includes a trend graph of a first-category parameter, the first information also includes fourth parameter data for a fourth-category parameter, where the fourth parameter data is parameter data of the fourth-category parameter associated with the first moment. The fourth-category parameter may be a parameter not displayed in the first display area 10a and / or a parameter associated with the first-category parameter. For example, the first-category parameters include physiological parameters such as heart rate and blood oxygen, and the first display area 10a currently displays a heart rate trend graph and a blood oxygen trend graph. The fourth-category parameter is a ventilation parameter of a ventilation device. After determining the first moment, the first information includes the heart rate value, blood oxygen value, and the parameter value of the ventilation parameter at the first moment.

[0109] When the first clinical information includes a marker 30 of an event, in some embodiments, the first information includes detailed information of a first target event, wherein the first target event is an event associated with the first moment in at least one event. Optionally, the first target event is an event that occurs to the patient within a first preset time period from the first moment. Exemplarily, when the first target event is an abnormal physiological state event of the patient, the detailed information of the first target event includes but is not limited to the cause and manifestation of the abnormal physiological state; when the first target event is an examination event experienced by the patient, the detailed information of the first target event includes but is not limited to data and imaging data obtained through detection; when the first target event is an inspection event experienced by the patient, the detailed information of the first target event includes but is not limited to data and imaging data obtained through inspection and analysis; when the first target event is a treatment event experienced by the patient, the detailed information of the first target event includes but is not limited to the means of treatment, physiological parameters before and after treatment, etc.

[0110] When the first clinical information includes an event mark 30, in other embodiments, the first information includes an access entry for the first target event, and the access entry for the first target event is used to provide detailed information of the first target event in response to a user's operation. For example, the user can click on the access entry to cause the display interface to jump to display detailed information of the first target event.

[0111] When the second clinical information includes a trend graph of a second-category parameter, the second information includes second parameter data for the second-category parameter, where the second parameter data is parameter data of the second-category parameter associated with the first moment. In some embodiments, the second parameter data is parameter data of the second-category parameter at the first moment. It will be understood that if the second clinical parameter includes multiple second-category parameters, multiple pieces of second parameter data may be provided.

[0112] In some embodiments, when the second clinical information includes a trend graph of a second-category parameter, the second information also includes fifth parameter data for a fifth-category parameter, where the fifth parameter data is parameter data of the fifth-category parameter associated with the first moment. The fifth-category parameter may be a parameter not displayed in the second display area 10b and / or a parameter associated with the second-category parameter. For example, the second-category parameters include physiological parameters such as heart rate and blood oxygen, and the second display area 10b currently displays a heart rate trend graph and a blood oxygen trend graph. The fifth-category parameter is a ventilation parameter of a ventilation device. After determining the first moment, the second information includes the heart rate value, blood oxygen value, and the parameter value of the ventilation parameter at the first moment.

[0113] When the second clinical information includes a marker 30 of an event, in some embodiments, the second information includes detailed information of a second target event, wherein the second target event is an event associated with the first moment in at least one event. Optionally, the second target event is an event that occurs to the patient within a second preset time period from the first moment. Exemplarily, when the second target event is an abnormal physiological state event of the patient, the detailed information of the second target event includes but is not limited to the cause and manifestation of the abnormal physiological state; when the second target event is an examination event experienced by the patient, the detailed information of the second target event includes but is not limited to data and imaging data obtained through detection; when the second target event is an inspection event experienced by the patient, the detailed information of the second target event includes but is not limited to data and imaging data obtained through inspection and analysis; when the second target event is a treatment event experienced by the patient, the detailed information of the second target event includes but is not limited to the means of treatment, physiological parameters before and after treatment, etc.

[0114] When the second clinical information includes the event mark 30, in other embodiments, the second information includes an access entry for the second target event, and the access entry for the second target event is used to provide detailed information of the second target event in response to the user's operation. For example, the user can click on the access entry to cause the display interface to jump to display detailed information of the second target event.

[0115] Step A500: Display the first information and the second information in a set manner on the display interface.

[0116] In some embodiments, the first information is displayed in the first display area 10a, and the second information is displayed in the second display area 10b. That is, similar to the first clinical information and the second clinical information, the first information and the second information are displayed in the two display areas, respectively. For example, when the first clinical information includes a trend graph of a first-category parameter and the first information includes first parameter data, the first parameter data is displayed near the location corresponding to the first parameter data on the trend graph of the first-category parameter, so that the first parameter data is in a more prominent position; when the first information includes detailed information or an access portal for a first target event, the detailed information or access portal for the first target event is displayed in a blank area of ​​the first display area 10a. When the second clinical information includes a trend graph of a second-category parameter and the second information includes second parameter data, the second parameter data is displayed near the location corresponding to the second parameter data on the trend graph of the second-category parameter, so that the second parameter data is in a more prominent position; when the second information includes detailed information or an access portal for a second target event, the detailed information or access portal for the second target event is displayed in a blank area of ​​the second display area 10b.

[0117] In some embodiments, as shown in Figure 8, a first window 50a is created in the display interface, and the first information and the second information are displayed in the first window 50a. The user can view all information related to the first moment in one window. For example, when the first clinical information includes a trend graph of a first type of parameter, and the second clinical information includes a trend graph of a second type of parameter, the first parameter data and the second parameter data are displayed simultaneously in the first window 50a; when any of the first clinical information and the second clinical information includes an event mark 30, the first window 50a also displays detailed information of the first target event, or also displays an access entrance to the first target event.

[0118] In some embodiments, as shown in FIG9 , a second window 50 b and a third window 50 c are created within the display interface, with the first information displayed within the second window 50 b and the second information displayed within the third window 50 c. In other words, the first information and the second information are displayed within two different windows. In some embodiments, when the first display area 10 a also includes a first reference cursor 40 a, after the user determines the first moment, the first reference cursor 40 a is moved to a position on the first timeline 20 a corresponding to the first moment, and a second window 50 b is created near the first reference cursor 40 a. This establishes a connection between the second window 50 b and the first reference cursor 40 a indicating the first moment, allowing the user to more intuitively perceive the relationship between the first information and the first moment. Furthermore, a third window 50 c may also be created simultaneously near the first reference cursor 40 a. In some embodiments, when the second display area 10b also includes a second reference cursor 40b, after the user determines the first moment, the second reference cursor 40b is also moved to a position corresponding to the first moment on the second time axis 20b, and a third window 50c is created near the second reference cursor 40b. This is equivalent to establishing a connection between the third window 50c and the second reference cursor 40b indicating the first moment, so that the user can more intuitively feel the relationship between the second information and the first moment. In addition, a second window 50b can also be created near the second reference cursor 40b at the same time.

[0119] In some embodiments, the display interface further includes a third display area 10c that is independent of the first display area 10a and the second display area 10b, and displays the first information and the second information in the third display area 10c. For example, when the first clinical information includes a trend graph of a first type of parameter, and the second clinical information includes a trend graph of a second type of parameter, the first parameter data and the second parameter data are simultaneously displayed in the third display area 10c; when either the first clinical information or the second clinical information includes an event marker 30, the third display area 10c also displays detailed information about the first target event, or displays an access portal to the first target event. The third display area 10c and the fourth display area 10d may be the same or different.

[0120] To further illustrate the technical solution of the above embodiment, please first refer to Figures 10 to 12. Figures 10 to 12 are schematic diagrams of display interfaces for target physiological structures, namely the circulatory system, respiratory system, and nervous system. The target physiological structure is the physiological structure corresponding to the display interface, and the information in each display interface is associated with the target physiological structure. These five target physiological structures can be switched using the toggle bar at the top of Figures 10 to 12. In addition, in this embodiment, each display area is displayed in the form of cards; for example, a display area can include one or more cards. Each display interface includes a first display area 10a, two second display areas (10b1, 10b2), an overview information area 10f, and a target management area 10g. It should be noted that the first display area 10a and the second display area (10b1, 10b2) in Figures 10 to 12 are relative concepts. For example, it can also be said that each display interface includes two first display areas 10a and one second display area 10b. The above is only an example, and the embodiment of the present application does not limit which of 10a, 10b1, and 10b2 in the specific figure is the first display area and which one or more are the second display areas.

[0121] The first display area 10a in Figures 10 to 12 includes trend graphs of multiple first-category parameters and multiple event markers 30. Furthermore, the first display area 10a is used to display real-time parameter data corresponding to the first-category parameters. The multiple event markers 30 and the trend graphs of the multiple first-category parameters share a first time axis 20a. The multiple trend graphs are divided into at least two trend groups, each of which includes at least one trend graph of the first-category parameter. Each trend group has a corresponding trend group identifier and a toggle display control for folding and displaying the trend graphs in the trend group. When a trend graph in a trend group is displayed, if a user inputs an open / close operation on the toggle display control, the trend graph in the trend group is folded. When a trend graph in a trend group is folded, if a user inputs an open / close operation on the toggle display control, the folded trend graph in the trend group is displayed. In other words, the trend graphs in each trend group can be folded and expanded. This has the advantage of using the concept of trend groups to centrally present clinically relevant parameters, making it easier for users to compare and analyze parameter data from multiple groups of parameters. Taking the first display area 10a of the display interface of the circulatory system as an example, as shown in Figures 13 and 14, it includes several trend groups, including vital sign trend group, input and output group, vasoactive drug group and sedative drug group. Among them, the trend group icons of the "vital sign trend", "input and output", "vasoactive drug" and "sedative drug" trend groups, and the lower triangle on the left side of the trend group icon is a switch display control. Each trend group can be expanded or collapsed to adapt to more clinical diagnosis and treatment scenarios. For example, in Figure 14, the vasoactive drug group and the sedative drug group are folded. For example, when the user needs to view the impact of vasoactive drugs on blood pressure, the "input and output" trend group can be folded to present the vital sign parameter group and the vasoactive drug trend group together, helping the user to compare data more flexibly.

[0122] FIG15 is a schematic diagram showing a second window 50 b created near the first reference cursor 40 a , wherein first parameter data of the first type of parameters are displayed in the second window 50 b .

[0123] The second display area 10b1 includes a plurality of trend graphs of the second type of parameters, and the trend graphs of the second type of parameters are discrete trend graphs. For example, in FIG11 , the second type of parameters include PaO2 / FiO2, PaO2, PaCO2, and pH.

[0124] The second display area 10b2 includes multiple event markers 30 arranged vertically. These events are events associated with the target physiological structure. In some embodiments, by clicking on the event marker 30 in the second display area 10b2, the user can view the patient's vital sign waveforms and parameters at the time of the event corresponding to the marker 30, and understand the full picture of the event. For example, in the second display area 10b2 of the circulatory system in Figure 10, after the user clicks on the marker 30 corresponding to the abnormal event indicating abnormal blood oxygen, the second display area 10b2 expands and displays the trend graph of the blood oxygen. It is also possible to expand and view the patient's complete event list through operations in the second display area 10b2 to meet the user's data analysis needs in different dimensions.

[0125] The overview information area 10f is used to display overview information of the target physiological structure. This overview information includes, but is not limited to, statistical information on the parameter data of the patient's important physiological parameters (at least one of the following: fluctuation range, cumulative count, maximum value, minimum value, and mean value over a period of time); abnormal statistics of the target physiological structure (such as the frequency, number, or percentage of parameter data exceeding the normal range, or examples such as arrhythmia or abnormal lactate levels); abnormal values ​​of the parameter data of the first category of clinical parameters; risk prediction information generated based on the parameter data of the first category of clinical parameters (such as possible heart failure); and at least one of the following: diagnostic and treatment recommendations generated based on the parameter data of the first category of clinical parameters (such as recommendations for ultrasound examination or attention to blood pressure fluctuations). In some embodiments, the third category of parameters includes the first and second category parameters. As can be seen, the overview information area 10f can present core parameters or indicators of the target physiological structure in a visual graphical format, helping users quickly access key information. At the same time, as a macroscopic representation of the system or organ, the overview information area 10f can help users quickly understand the macroscopic status through eye-catching visual representations. For example, the background or icon of the overview information area 10f may be red when abnormal, and green when normal. In some embodiments, the overview information area 10f may also display the specific parameter ranges of parameter data of some third-category parameters through various methods such as bar charts, bar graphs, and spider graphs.

[0126] The overview information area 10f will be described below with reference to FIG. 10 and FIG. 11 .

[0127] Figure 10 shows the display interface corresponding to the circulatory system. In the overview information area 10f, the parameter changes in the circulatory system over a period of time are first shown in the form of a curve chart from top to bottom, from which the abnormal values ​​of the parameter data in the circulatory system can also be seen. In addition, in the circulatory summary: numerical statistics such as heart rate and blood pressure are statistical information on the parameter data of important physiological parameters in the circulatory system; the description of the shock index and circulatory status is a statistical analysis of abnormal states of the circulatory system; the description of the shock index, "a period of shock or severe shock is possible", and the description of the circulatory status, "the risk of worsening circulation" are risk prediction information for the circulatory system. In the circulatory perfusion card, the SI value is calculated according to the corresponding rules, and the GCS score is calculated according to the GCS scoring rules.

[0128] Figure 11 shows the respiratory system display interface. In the overview information area 10f, statistical information on important physiological parameters of the respiratory system is displayed to the right of the lung graphic. In the respiratory summary, "Consider adjusting ventilation support mode or parameters" provides diagnostic and treatment recommendations for the respiratory system, while "Presence of pressure risk" provides risk prediction information for the respiratory system.

[0129] The target management area 10g is used to display the distribution statistics of the fourth-category parameter in at least two parameter intervals. The distribution statistics are used to indicate the achievement of the fourth-category parameter against the preset target. The fourth-category parameter can be partially identical to the first-category parameter and the second-category parameter, or can be completely identical. For example, Figure 17 shows the target management area 10g of the circulatory system display interface. It can be seen that there are five parameter intervals for heart rate over the past 20 hours and 30 minutes, of which the cumulative duration of time in which the heart rate fell within the parameter interval of 60 to 100 was 60%.

[0130] In some embodiments, medical personnel can customize target statistics of specific parameters that need to be viewed under the target physiological structure, customize the specific target range, and the detailed rules for segmented statistics of the parameter.

[0131] In some embodiments, the target management area 10g can also be expanded, as shown in Figure 18, and a trend chart of the fourth type of parameters can be displayed. Moreover, when the user selects a fourth type of parameter interval, the corresponding trend chart can display the time periods in which the fourth type of parameters fall into the parameter interval. In other words, a more detailed target statistical distribution and its association with the fourth type of parameter trend can be presented, as well as the distribution of these fourth type of parameters in different time periods.

[0132] In some embodiments, the display interface expresses the macroscopic state of the patient as a whole and / or the target physiological structure in various ways to assist the user in quickly grasping the overall situation of the patient as a whole and / or the target physiological structure. Specifically, the macroscopic state of the patient as a whole and / or the target physiological structure can be expressed in one or more of the above-mentioned display areas. For example, the macroscopic state of the patient as a whole can be expressed in one display area, and the macroscopic state of the target physiological structure can be expressed in another display area. Alternatively, both the macroscopic state of the patient as a whole and the macroscopic state of the target physiological structure can be expressed in the same display area. In some embodiments below, the overview information area 10f is used to express the macroscopic state of the patient as a whole and / or the target physiological structure as an example. For example, information about the macroscopic state is displayed in the overview information described above.

[0133] In some embodiments, when the overview information area 10f expresses the overall macroscopic state of the patient, if there is no abnormality in any of the patient's physiological structures, the background or icon of the overview information area 10f is green; when the number of abnormal physiological structures of the patient exceeds a preset threshold, or the degree of abnormality of a certain physiological structure exceeds a preset threshold, the background or icon of the overview information area 10f is red.

[0134] In some embodiments, when the overview information area 10f expresses the macroscopic state of the target physiological structure, there are several possibilities: when the target physiological structure is a physiological system of the patient, the overview information area 10f can express the macroscopic state of the physiological system; when the target physiological structure is a physiological organ of the patient, the overview information area 10f can express the macroscopic state of the physiological system; when the target physiological structure is a tissue of the patient, the overview information area 10f can express the tissue state of the patient; when the target physiological structure is a feature of a physiological system or a physiological organ of the patient, the overview information area 10f can express the macroscopic state of the feature. For example, when an abnormality occurs in the target physiological structure, the background or icon state of the overview information area 10f is red to indicate that the macroscopic state of the target physiological structure is abnormal; when the target physiological structure is generally normal, the background or icon state of the overview information area 10f is green.

[0135] In some embodiments, the overview information area 10f is used to display the assessment results of the patient's status to reflect the overall macroscopic status of the patient or the macroscopic status of the target physiological structure, wherein the patient's status may include the status of the patient as a whole and / or the target physiological structure, that is, the patient's status includes one or more clinically defined states of the patient as a whole, the physiological system, the physiological organ, the physiological part, the tissue, the characteristics of the physiological system and the characteristics of the physiological organ, reflecting the physiological function of the part, such as circulatory instability and insufficient perfusion of the circulatory system.

[0136] In some embodiments, the evaluation result of the patient's state can be a prediction result of the patient's future state, or a judgment result of the patient's current state. For example, a patient state such as "circulatory instability" in the drawings or text of this application can refer to the patient's current circulatory instability, or it can refer to the patient's possible circulatory instability in the future. The prediction result of the patient's future state represents the development trend of the patient's state. Presenting the prediction result of the patient's future state helps medical staff intervene early to avoid or slow down the deterioration of the patient's state. Presenting the judgment result of the patient's current state also helps medical staff to carry out targeted treatment in a timely manner.

[0137] The results of the patient status assessment can be displayed in various ways, specifically:

[0138] In some embodiments, the assessment results of the patient's status can be displayed in the form of text, graphics, or a combination of the two. When using text, character strings related to the patient's status can be pre-configured, including character strings that characterize the patient's overall or target physiological structure, as well as character strings that characterize specific statuses, such as circulatory system + possible shock / possible heart failure / possible internal bleeding, respiratory system + possible respiratory depression, nervous system + possible intracranial hemorrhage, urinary system + possible renal failure, immune system + possible severe infection, etc. The character string can be in various forms, as long as it can reflect the patient's status. For example, the character string used to characterize heart failure can be "the circulatory system may have heart failure", "the patient may have heart failure", "the patient is at risk of heart failure", etc. The character string can be pre-set by an expert for each patient's status, or adjusted using natural language processing-related methods to adapt to the current specific patient status. Exemplarily, the character string can also allow the user to configure or modify it.

[0139] When a graphical representation is used, a graphic associated with each patient condition that can vividly represent the patient condition can be pre-stored and called upon for display after the patient condition is determined. The graphic representing the patient condition can correspond to the patient's entire body or a target physiological structure, and the graphic can be labeled to represent the patient's condition using at least one of symbolic information, color information, and textual information located on or near the graphic. Exemplarily, in Figures 10 to 12, the patient status is represented by a status graphic 60. Specifically, in Figure 10, the status graphic 60 simulates the organs included in the circulatory system to vividly represent the circulatory system. When the status graphic 60 is green, it indicates that the circulatory system is in a normal state. When the status graphic 60 is red, it indicates that the circulatory system is in an abnormal state. In Figure 11, the status graphic 60 includes a graphic of a lung lobe to vividly represent the respiratory system. When the status graphic 60 is green, it indicates that the respiratory system is in a normal state. When the status graphic 60 is red, it indicates that the respiratory system is in an abnormal state. In addition, the characters "unstable breathing" are displayed on the right side of the status graphic 60 to indicate the current abnormality of the respiratory system. In Figure 12, the status graphic 60 includes a graphic of a brain to vividly represent the nervous system. When the status graphic 60 is green, it indicates that the nervous system is in a normal state. When the status graphic 60 is red, it indicates that the nervous system is in an abnormal state.

[0140] In some embodiments, the patient status includes the deterioration state of the patient's overall condition or a target physiological structure, such as whether the target physiological structure is currently deteriorating or is likely to deteriorate in the future. In some embodiments, the patient status may also include whether the patient's overall condition or the target physiological structure is abnormal, the level of abnormality, the criticality level, the level of care, etc. For example, the circulatory system status may include abnormal circulation or normal circulation, and abnormal circulation may further include mild abnormal circulation or severe abnormal circulation. For example, in the overview information area 10f of Figure 10, the characters "Circulatory status has a risk of deterioration" indicate that the circulatory system may deteriorate in the future. Optionally, the patient status may also include specific diseases related to the patient's overall condition or the target physiological structure, such as acute respiratory distress syndrome (ARDS), respiratory failure, acute kidney injury (AKI), sepsis, heart failure, brain damage, etc. Illustratively, the patient status may also include an unknown state or a suspected abnormal state.

[0141] For example, the patient's condition can be assessed based on specific, clinically established, and consensus-based assessment rules to obtain an assessment result. For example, a patient's score can be obtained using scoring rules such as the SOFA (Sequential Organ Failure Assessment) score or the NEWS (United Kingdom Early Warning System) score, and this score can be used as the assessment result. Alternatively, the patient's condition can be assessed based on specific scoring rules configured through clinical research or other means. For example, when parameter data for a first category of clinical parameters meets one or more preset rules, the patient is determined to have a patient condition corresponding to the preset rules. Alternatively, the patient's condition can be assessed using a machine learning model. Alternatively, the patient's condition can be assessed by integrating data from multiple parameters to obtain an accurate and reliable assessment result.

[0142] In some embodiments, when the patient status includes the overall status of the patient, the evaluation result can be judged based on at least one of the following: the patient's criticality, the type of patient's illness, the stability of the patient's status, the type of department the patient is in, the location of the patient's ward, the patient's bed number, the role of the patient's attending physician, the clinical operations performed by the medical staff on the patient, the information related to the patient's level judgment pre-entered by the medical staff, the patient's admission time, the type or dosage of the drug taken by the patient, the cardiopulmonary status grading assessment result, the SOFA score, the NEWS score or the score entered by the user, etc.

[0143] The SOFA score aims to describe the onset, progression, and incidence of multi-organ dysfunction. It includes six scoring components: respiratory, hematologic, hepatic, cardiovascular, central nervous, and renal. Each component is scored from 0 to 4, and the sum of these scores is the total SOFA score. A higher score indicates a worse prognosis. The NEWS score includes six components: respiratory rate, oxygen saturation, temperature, systolic blood pressure, pulse, and level of consciousness. Each component is scored from 0 to 3, with an additional 2 points added if the patient requires oxygen. The sum of these scores is the total NEWS score. The cardiopulmonary status grading assessment is based on both respiratory and circulatory assessments. A high score indicates a high severity if either respiratory or circulatory instability is high, an intermediate score indicates neither respiratory or circulatory instability is high, and a low score indicates no respiratory or circulatory instability. Higher scores indicate more severe disease.

[0144] In addition, the patient status assessment result may also be an assessment result under other assessment criteria, or a score manually set by the user based on subjectivity.

[0145] In some embodiments, multiple patients can be divided into multiple patient levels with different degrees of criticality based on the patient status assessment results, and the level identifier used to indicate the level is displayed in the overview information area 10f. Patients with higher criticality can have higher priorities, but are not limited to this. In some embodiments, the same level can be set for different assessment results, such as high, medium and low. In some embodiments, the number of levels is not limited to three. For example, the patient's level can also include only the first level and the second level, or a fatal level can be set above the high level. Grading can be performed based solely on the patient status assessment results, or the patient status assessment results can be combined with other patient information for grading.

[0146] For example, when grading based on the SOFA score, a score greater than or equal to 5 is classified as high. A score greater than or equal to 2, combined with concurrent use of vasopressors, a mean arterial pressure (MAP) ≥ 65 mmHg, and serum lactate > 2 mmol is also classified as high. A score between 2 and 4 is classified as intermediate, and a score between 0 and 1 is classified as low. When grading based on the NEWS score, a score greater than or equal to 7 is classified as high, a score between 5 and 6, or a score of 3 for any individual indicator, is classified as intermediate, and a score between 0 and 4 is classified as low. The cardiopulmonary status grading results are already categorized as low, intermediate, and high, and can be used directly. For manually entered scores, the grading rules can also be user-defined. Alternatively, a comprehensive assessment of the level can be performed using two or more of the aforementioned grading rules.

[0147] In some embodiments, when the patient status includes the overall status of the patient, when the criticality is high, the level is identified by the Roman numeral "I"; when the criticality is intermediate, the level is identified by the Roman numeral "II"; when the criticality is low, the level is identified by the Roman numeral "III".

[0148] In some embodiments, when the patient status includes the status of the target physiological structure, the criticality can be represented by a graphic. For example, the criticality of the target physiological structure can also be represented by the above-mentioned status graphic 60. For example, in Figure 10, the target physiological structure is the circulatory system, and the color of the status graphic 60 can represent the criticality of the circulatory system. When the status graphic 60 is green, it means that the criticality of the circulatory system is low. When the status graphic 60 is yellow, it means that the criticality of the circulatory system is medium. When the status graphic 60 is red, it means that the criticality of the circulatory system is high. In Figure 11, the target physiological structure is the respiratory system. The color of the status graphic 60 can represent the criticality of the respiratory system. When the status graphic 60 is green, it means that the criticality of the respiratory system is medium. The criticality level of the respiratory system is low. When the status graphic 60 is yellow, it indicates that the criticality level of the respiratory system is medium. When the status graphic 60 is red, it indicates that the criticality level of the respiratory system is high. In Figure 12, the target physiological structure is the nervous system. The color of the status graphic 60 can indicate the criticality level of the nervous system. When the status graphic 60 is green, it indicates that the criticality level of the nervous system is low. When the status graphic 60 is yellow, it indicates that the criticality level of the nervous system is medium. When the status graphic 60 is red, it indicates that the criticality level of the nervous system is high.

[0149] It can be understood that when the patient status includes the overall status of the patient, the degree of criticality can also be represented by graphics, as in Figures 10 to 12. For example, a graphic of a human body is displayed in any display area, and different degrees of criticality are distinguished by changing the display method of the graphic; and when the patient status includes the status of the target physiological structure, different degrees of criticality can also be distinguished by numbers or scores instead of graphics.

[0150] Based on the above medical device, as shown in FIG19 , another embodiment of the present application provides a display processing method, including:

[0151] Step B100: Obtain first clinical information of the patient.

[0152] The first clinical information in this step refers to clinically relevant information, including but not limited to monitoring information, infusion information, and alarm information. The first clinical information can be collected and acquired through sensors on the medical device itself, third-party devices, application software, or user input.

[0153] Step B200: Display the first clinical information on the display interface. In some embodiments, the display interface has a first display area 10a, and the first clinical information is displayed in the first display area 10a.

[0154] In some embodiments, as shown in FIG20 , the first clinical information includes a trend graph of a first-category parameter. That is, the first clinical information can reflect the historical trend of the first-category parameter. Depending on the type of trend graph, the trend graph of the first-category parameter may include, but is not limited to, a curve graph, a line graph, etc. Depending on the type of parameter data, the trend graph may also have different forms. In some embodiments, if the parameter data of the first-category parameter is continuous data, the trend graph of the first-category parameter is a continuous trend graph. In other embodiments, if the parameter data of the first-category parameter is discrete data, the trend graph of the first-category parameter is a discrete trend graph. When the first clinical information includes multiple trend graphs of the first-category parameter, the multiple trend graphs of the first-category parameter may share the same first timeline 20a. For example, the multiple trend graphs of the first-category parameter may be arranged side by side above the first timeline 20a. That is, multiple information of the same type may share the same timeline. The first timeline 20a may be displayed in the first display area 10a or may be hidden.

[0155] In some embodiments, as shown in FIG21 , the first clinical information includes, in addition to a trend graph of the first type of parameter, markers 30 for events associated with the patient. These events include, but are not limited to, abnormal physiological state events, examination events, test events, and treatment events experienced by the patient. It is understood that these events are also time-related. For example, if the patient's physiological state is abnormal at time A, then time A is defined as the time when the abnormal physiological state event occurred. For another example, if an ultrasound examination is performed on the patient at time B and ultrasound image data is obtained, then at time B the patient experienced an examination event. For another example, if a routine blood test is performed on the patient at time C and a routine blood test result is obtained, then at time C the patient experienced a test event. For another example, if a therapeutic drug is infused into the patient at time D, then at time D the patient experienced a treatment event. In some embodiments, markers 30 for different types of events are displayed differently. For example, markers 30 for abnormal physiological state events are displayed in red, while markers 30 for test events are displayed in blue.

[0156] As can be seen from the above description, the aforementioned events and time are also related, and the event markers 30 can also be sorted according to chronological order. In some embodiments, the event markers 30 in the first display area 10a can be distributed along the first time axis 20a, that is, multiple information of different types also share the same time axis. When there are multiple event markers 30, the event markers 30 can form event bars along the first time axis 20a. In some embodiments, the event markers 30 of different types form different event bars. For example, the markers 30 for abnormal physiological state events form one event bar parallel to the first time axis 20a, while the markers 30 for examination events form another event bar parallel to the first time axis 20a.

[0157] In some embodiments, the first clinical information may further include a marker 30 of an event, but does not include a trend graph of the first category of parameters.

[0158] Step B300: receiving a first selection operation input by the user to determine a first time, and receiving a second selection operation input to determine a second time different from the first time.

[0159] In some embodiments, the first selected operation is an operation performed by the user in the first display area 10a. Based on the above description of the first clinical information, the first selected operation input by the user includes at least the following methods:

[0160] When the first clinical information includes a trend graph of a first type of parameter, in some embodiments, the first display area 10a includes an area for the user to select a point. When the user selects any point in the area, the first moment can be determined based on the corresponding position of the point on the first time axis 20a; in other embodiments, when the trend graph of the first type of parameter is a continuous trend graph, the user can select any point on the trend graph, and the first moment can be determined based on the corresponding position of the point on the first time axis 20a; when the trend graph of the first type of parameter is a discrete trend graph, the user can first select a discrete point on the trend graph, and then determine the first moment based on the position of the discrete point on the first time axis 20a.

[0161] When the first clinical information includes a trend graph of a first type of parameter, in some embodiments, as shown in Figures 20 and 21, the first display area 10a also includes a first reference cursor 40a movable along the first time axis 20a, and the user can determine the first moment by dragging the first reference cursor 40a. For example, the user drags the first reference cursor 40a to a certain position along the first time axis 20a and enters a confirmation instruction, and the first moment can be determined according to the position of the first reference cursor 40a on the first time axis 20a.

[0162] When the first clinical information includes an event mark 30, in some embodiments, the user can determine the first moment by selecting any mark 30. For example, if the user selects an abnormal physiological state event, the moment when the abnormal physiological state event occurs is taken as the first moment.

[0163] In some embodiments, the second selection operation is also an operation performed by the user in the first display area 10a. Based on the above description of the first clinical information, the second selection operation input by the user includes at least the following methods:

[0164] When the first clinical information includes a trend graph of a first type of parameter, in some embodiments, the first display area 10a includes an area for the user to select a point. When the user selects any point in the area, the second moment can be determined based on the corresponding position of the point on the first time axis 20a; in other embodiments, when the trend graph of the first type of parameter is a continuous trend graph, the user can select any point on the trend graph, and the second moment can be determined based on the corresponding position of the point on the first time axis 20a; when the trend graph of the first type of parameter is a discrete trend graph, the user can first select a discrete point on the trend graph, and then determine the second moment based on the position of the discrete point on the first time axis 20a.

[0165] When the first clinical information includes a trend graph of the first category of parameters, in some embodiments, as shown in Figures 20 and 21, the first display area 10a also includes a third reference cursor 40c movable along the first time axis 20a, and the user can determine the second moment by dragging the third reference cursor 40c. For example, the user drags the third reference cursor 40c to a certain position along the first time axis 20a and enters a confirmation instruction, and the second moment can be determined according to the position of the third reference cursor 40c on the first time axis 20a.

[0166] When the first clinical information includes event marks 30, in some embodiments, the user can determine the second moment by selecting any mark 30. For example, if the user selects an abnormal physiological state event, the abnormal physiological state event will be used as the second moment.

[0167] In some embodiments, the display interface also includes a fifth display area 10e that is independent of the first display area 10a and the second display area 10b. The first selection operation and / or the second selection operation is an operation performed by the user in the fifth display area 10e. That is, the user can determine the first moment and the second moment associated with the first clinical information by inputting a selection operation in other display areas in the display interface.

[0168] Step B400: Obtain first information associated with the first moment and corresponding third information associated with the second moment corresponding to the first clinical information.

[0169] If the first clinical information includes trend graph information, the corresponding first information includes parameter data associated with the trend graph at the first moment, and the corresponding third information includes parameter data associated with the trend graph at the second moment. For example, when the first clinical information includes a trend graph of a first type of parameter, the first information includes first parameter data of the first type of parameter, where the first parameter data is parameter data associated with the first moment, and the third information includes third parameter data of the first type of parameter, where the third parameter data is parameter data associated with the second moment.

[0170] In some embodiments, the first parameter data is the parameter data of the first category parameter at the first moment, and the third parameter data is the parameter data of the first category parameter at the second moment. It can be understood that if the first clinical information includes trend graphs of multiple first category parameters, there can be multiple first parameter data and multiple third parameter data.

[0171] When the first clinical information includes an event marker 30, in some embodiments, the first information includes detailed information about a first target event, wherein the first target event is an event associated with the first moment in time among at least one event. Optionally, the first target event is an event that occurs within a first preset time interval from the first moment in time. For example, when the first target event is an abnormal physiological state event of the patient, the detailed information about the first target event includes, but is not limited to, the cause and manifestations of the abnormal physiological state; when the first target event is an examination event experienced by the patient, the detailed information about the first target event includes, but is not limited to, data and imaging data obtained through the examination; when the first target event is a test event experienced by the patient, the detailed information about the first target event includes, but is not limited to, data and analysis obtained through the test; when the first target event is a treatment event experienced by the patient, the detailed information about the first target event includes, but is not limited to, the treatment method, physiological parameters before and after treatment, etc. In other embodiments, the first information includes an access portal to the first target event, which is used to provide detailed information about the first target event in response to a user operation. For example, by clicking on the access portal, the user can cause the display interface to jump to displaying detailed information about the first target event.

[0172] When the first clinical information includes an event marker 30, in some embodiments, the third information includes detailed information about a third target event, wherein the third target event is an event associated with the second moment in time among at least one event. Optionally, the third target event is an event that occurs within a third preset time interval between the patient and the second moment in time. For example, when the third target event is an abnormal physiological state of the patient, the detailed information about the third target event includes, but is not limited to, the cause and manifestations of the abnormal physiological state; when the third target event is an examination event experienced by the patient, the detailed information about the third target event includes, but is not limited to, data and imaging data obtained through the examination; when the third target event is a test event experienced by the patient, the detailed information about the third target event includes, but is not limited to, data and analysis obtained through the test; when the third target event is a treatment event experienced by the patient, the detailed information about the third target event includes, but is not limited to, the treatment method and physiological parameters before and after treatment. In other embodiments, the third information includes an access portal to the third target event, which is used to provide detailed information about the third target event in response to a user operation. For example, by clicking on the access portal, the user can cause the display interface to jump to displaying detailed information about the third target event.

[0173] Step B500: Compare and display the first information and the third information corresponding to the first clinical information in the display interface.

[0174] In some embodiments, a fourth window 50d is created in the display interface, and the first information and the third information corresponding to the first clinical information are compared and displayed in the fourth window 50d. For example, when the first clinical information includes a trend graph of a first category parameter, the first information includes first parameter data, and the third information includes third parameter data, then the first parameter data and the third parameter data of the same first category parameter can be displayed side by side in the fourth window 50d to compare the first information and the third information.

[0175] In some embodiments, a fifth window 50e and a sixth window 50f are created on the display interface, with the first information displayed in the fifth window 50e and the third information displayed in the sixth window 50f. In some embodiments, as shown in FIG21 , when the display interface includes a first reference cursor 40a movable along the first time axis 20a, after the user determines the first moment, the first reference cursor 40a is also moved to a position on the first time axis 20a corresponding to the first moment, and the fifth window 50e is created near the first reference cursor 40a. This establishes a connection between the fifth window 50e and the first reference cursor 40a indicating the first moment, allowing the user to more intuitively perceive the relationship between the first information and the first moment. In some embodiments, as shown in Figure 21, when the display interface includes a third reference cursor 40c that can be moved along the first time axis 20a, after the user determines the second moment, the third reference cursor 40c is also moved to a position on the first time axis 20a corresponding to the second moment, and a sixth window 50f is created near the third reference cursor 40c. This is equivalent to establishing a connection between the sixth window 50f and the third reference cursor 40c indicating the second moment, so that the user can more intuitively feel the relationship between the third information and the first moment.

[0176] Optionally, the comparison and display of the first information and the third information may include but is not limited to at least one of changes in previous and subsequent data, highlighting of key data, highlighting of data exceeding a threshold value / preset condition, etc.

[0177] On the one hand, the three types of information displayed in the comparison can be distinguished by at least one of font color, font size, and background color. For example, the change in font color of the previous and subsequent data is used as an example for explanation: for example, the first information is in green font and the third information is in red font; another example is that the same data in the first and third information are in the same font color, and the data that has increased is in red font and the data that has decreased is in green font; another example is that the data in the first and third information are in the same font color, and the data that has increased is in red font and the data that has decreased is in green font; for example, the data in the first and third information are in the same font color, and the first mark is added to the data that has increased and the second mark is added to the data that has decreased, for example, the first mark is an upward arrow and the second mark is a downward arrow. The optional arrow colors of the first and second marks can also be used to distinguish, which is not limited here.

[0178] On the other hand, the change between the previous and next data can also be calculated according to preset rules for calculable data, such as subtraction operation, and the obtained value is highlighted. The highlighting here is distinguished by at least one of font color, font size, and background color.

[0179] To further illustrate the technical solution of the above embodiment, please refer to FIG16. FIG16 is a schematic diagram of a first display area 10a according to an embodiment. The first display area 10a includes trend graphs of multiple first-category parameters and multiple event markers 30. A fourth window 50d is created near a third reference cursor 40c. The first parameter data and the third parameter data of the first-category parameters are displayed in the fourth window 50d.

[0180] In the above embodiment, after the user determines the first moment, the first information corresponding to the first clinical information and the second information corresponding to the second clinical information can be displayed simultaneously, or after the user determines the first moment and the second moment, the first information and the third information corresponding to the first clinical information can be compared and displayed, thereby providing the user with content of interest from two dimensions: the difference between different information and the comparison of the same information at different moments, thereby improving the user's work efficiency.

[0181] In the above-mentioned embodiments of the present application, different windows and different display areas are involved. The two are explained here. The window can be a newly created window in the display screen, which may block the original display interface (for example, block part of the content of the original display area); the display area is the area in the display screen used to display information, which can be understood as the area that can be divided / has been divided in the display screen.

[0182] Those skilled in the art will appreciate that all or part of the functions of the various methods in the above embodiments can be implemented by hardware or by computer program. When all or part of the functions in the above embodiments are implemented by computer program, the program can be stored in a computer-readable storage medium, and the storage medium can include: read-only memory, random access memory, disk, optical disk, hard disk, etc., and the program is executed by a computer to implement the above functions. For example, the program is stored in the memory of the device, and when the program in the memory is executed by the processor, all or part of the above functions can be implemented. In addition, when all or part of the functions in the above embodiments are implemented by computer program, the program can also be stored in a storage medium such as a server, another computer, disk, optical disk, flash disk or mobile hard disk, and saved in the memory of the local device by downloading or copying, or the system of the local device is updated. When the program in the memory is executed by the processor, all or part of the functions in the above embodiments can be implemented.

[0183] The above specific examples are used to illustrate the present invention, which are only used to help understand the present invention and are not intended to limit the present invention. For those skilled in the art, according to the concept of the present invention, the above specific embodiments can be modified.

Claims

1. A display processing method for medical equipment, characterized in that: include: obtaining first clinical information and second clinical information of the patient; Displaying the first clinical information in a first display area of ​​the display interface and displaying the second clinical information in a second display area of ​​the display interface; receiving a first selection operation input by a user to determine a first moment; Acquire first information associated with a first moment corresponding to the first clinical information, and acquire second information associated with the first moment corresponding to the second clinical information; The first information and the second information are displayed in a set manner on the display interface.

2. The method according to claim 1, wherein The displaying the first information and the second information in a set manner on the display interface includes: Displaying the first information in the first display area and displaying the second information in the second display area; or; creating a first window, and displaying the first information and the second information in the first window; or; creating a second window and a third window, displaying the first information in the second window and displaying the second information in the third window; or, A third display area within the display interface displays first information corresponding to the first clinical information and second information corresponding to the second clinical information. The third display area is independent of the first display area and the second display area.

3. The method according to claim 2, wherein The first clinical information is different from the second clinical information; The first clinical information includes any one or more types of information of the following types, and the second clinical information includes any one or more types of information of the following types: a trend graph of at least one parameter associated with the patient; A marker of at least one event associated with a patient; the at least one event comprises at least one of an abnormal physiological state event of the patient, an examination event, a test event, and a treatment event experienced by the patient.

4. The method according to claim 3, wherein If the first clinical information includes multiple pieces of information of the same type or different types, the multiple pieces of information share the same time axis; and / or If the second clinical information includes multiple pieces of information of the same type or different types, the multiple pieces of information share the same time axis.

5. The method according to claim 4, wherein A time axis shared by multiple pieces of information in the first clinical information is different from a time axis shared by multiple pieces of information in the second clinical information.

6. The method according to claim 3, wherein If any of the first clinical information and the second clinical information includes a trend graph of a first type of parameter, the corresponding information associated with the first moment includes: first parameter data of the first type of parameter, and the first parameter data is parameter data of the first type of parameter associated with the first moment.

7. The method according to claim 3, wherein If any of the first clinical information and the second clinical information includes a trend graph of a first type of parameter, the corresponding information associated with the first moment also includes fourth parameter data of a fourth type of parameter not included in the clinical information, and the fourth parameter data is parameter data of the fourth type of parameter associated with the first moment.

8. The method according to claim 3, wherein If any clinical information among the first clinical information and the second clinical information includes the mark of the at least one event, the corresponding information associated with the first moment includes: detailed information of the first target event or an access entrance of the first target event, the first target event is the event associated with the first moment in the at least one event, and the access entrance of the first target event is used to provide detailed information of the first target event in response to the user's operation.

9. The method according to claim 6, wherein If any of the first clinical information and the second clinical information includes a trend graph of a first type of parameter and the first information includes the first parameter data, displaying the first information in the first display area includes: The first parameter data is displayed near a position corresponding to the first parameter data on the trend graph.

10. The method according to any one of claims 2 to 9, wherein The first display area further includes a time axis and a reference cursor, wherein the reference cursor is movable along the time axis of the first display area; The creating the second window includes: creating the second window near the reference cursor.

11. The method according to claim 10, wherein The method further includes: based on the first selection operation, moving the reference cursor to a position on the time axis corresponding to the first moment.

12. The method according to claim 6, wherein If any of the first clinical information and the second clinical information includes a trend graph of a first type of parameter, the first display area is further used to display real-time parameter data corresponding to the first type of parameter.

13. The method according to claim 1, wherein The first selection operation is an operation performed by the user in any one of the first display area, the second display area, and the fourth display area, and the fourth display area is independent of the first display area and the second display area.

14. A display processing method for medical equipment, characterized in that: include: Obtain the patient's first clinical information; Displaying the first clinical information on a display interface; receiving a first selection operation input by a user to determine a first time, and receiving a second selection operation input to determine a second time different from the first time; Acquire first information associated with a first moment and corresponding third information associated with a second moment, corresponding to the first clinical information; The first information and the third information corresponding to the first clinical information are compared and displayed in the display interface.

15. The method according to claim 14, wherein The comparing and displaying the first information and the third information corresponding to the first clinical information in the display interface includes: creating a fourth window, comparing and displaying the first information and the third information corresponding to the first clinical information in the fourth window; or; creating a fifth window and a sixth window, displaying the first information in the fifth window and displaying the third information in the sixth window; or; When the first clinical information is displayed in the first display area, the first information and the third information corresponding to the first clinical information are compared and displayed in the fourth display area in the display interface, and the fourth display area is independent of the first display area.

16. The method according to claim 15, wherein The first clinical information includes any one or more types of information: a trend graph of at least one parameter associated with the patient; a marker of at least one event associated with the patient; The at least one event includes at least one of an abnormal physiological state event of the patient, an examination event, a test event, and a treatment event experienced by the patient.

17. The method according to claim 16, wherein If the first clinical information includes multiple pieces of information of the same type or multiple pieces of information of different types, the multiple pieces of information share the same time axis.

18. The method according to claim 16, wherein If the first clinical information includes trend graph type information, the corresponding first information includes: parameter data associated with the trend graph at the first moment, and the corresponding third information includes: parameter data associated with the trend graph at the second moment.

19. The method according to claim 16, wherein If the first clinical information includes a tag of the at least one event, the first information corresponding thereto includes: detailed information of a first target event or an access entry for the first target event, the first target event being an event associated with the first moment in the at least one event, the access entry for the first target event being used to provide detailed information of the first target event in response to a user operation; The corresponding third information includes: detailed information of the third target event or an access entrance to the third target event, wherein the third target event is an event among the at least one event associated with the second moment, and the access entrance to the third target event is used to provide detailed information of the third target event in response to the user's operation.

20. The method according to any one of claims 15 to 19, wherein The display interface further includes a time axis, a first reference cursor, and a third reference cursor, wherein the first reference cursor and the third reference cursor are movable along the time axis of the display interface; The creating of the fourth window comprises: creating the fourth window near the third reference cursor; The creating the fifth window includes: creating the fifth window near the first reference cursor; or The creating the sixth window includes: creating the sixth window near the third reference cursor.

21. The method according to claim 20, wherein The method also includes: based on the first selection operation, moving the first reference cursor to a position on the time axis of the display interface corresponding to the first moment; based on the second selection operation, moving the third reference cursor to a position on the time axis of the display interface corresponding to the second moment.

22. The method of claim 14, wherein When the first clinical information is displayed in the first display area, the first selection operation is an operation performed by the user in any one of the first display area and the fifth display area, and the fifth display area is independent of the first display area.

23. The method according to claim 1 or 14, wherein The display interface is further used to display the evaluation result of the patient's state to reflect the patient's macroscopic state, wherein the patient's state includes the state of the patient as a whole and / or the state of the target physiological structure.

24. The method according to claim 23, wherein When the patient status includes the overall status of the patient, the assessment result of the patient status is judged based on at least one of the following: the patient's criticality, the type of patient's illness, the stability of the patient's status, the type of department the patient is in, the location of the patient's ward, the patient's bed number, the role of the patient's attending physician, the clinical operations performed by the medical staff on the patient, the information related to the patient's level judgment pre-entered by the medical staff, the patient's admission time, the type or dosage of the medication taken by the patient, the cardiopulmonary status grading assessment result, the SOFA score, the NEWS score or the score entered by the user.

25. The method according to claim 23, wherein The target physiological structure is a patient's physiological system, physiological organ, physiological part, tissue, a feature of the physiological system, or a feature of the physiological organ.

26. The method according to claim 25, wherein The physiological system includes at least one of the musculoskeletal system, nervous system, endocrine system, circulatory system, respiratory system, digestive system, urinary system and reproductive system; the physiological organ includes at least one of the brain, heart, lungs, liver, stomach and kidneys; the physiological part includes at least one of the head, chest and abdomen; the tissue includes at least one of muscle tissue, nervous tissue and epithelial tissue; the characteristics of the physiological system or the characteristics of the physiological organ include at least one of coagulation, nutrition, infection and blood sugar.

27. A medical device, characterized in that: include: Memory, used to store programs; A processor, configured to implement the method according to any one of claims 1 to 26 by executing the program stored in the memory.

28. A computer-readable storage medium, characterized in that The medium stores a program, which can be executed by a processor to implement the method according to any one of claims 1 to 26.

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