CN117594180A

CN117594180A - Method for displaying medical data and life information processing system

Info

Publication number: CN117594180A
Application number: CN202311024000.0A
Authority: CN
Inventors: 谈琳; 章蕾; 潘瑞玲; 邹小玲; 代巍巍
Original assignee: Shenzhen Mindray Bio Medical Electronics Co Ltd
Current assignee: Shenzhen Mindray Bio Medical Electronics Co Ltd
Priority date: 2022-08-12
Filing date: 2023-08-14
Publication date: 2024-02-23

Abstract

A method of displaying medical data and a vital information processing system, the method comprising: obtaining a plurality of medical data of the medical object from at least two medical data sources for a preset time or a plurality of times; determining a plurality of clinical sections currently used, wherein the clinical sections correspond to physiological structures of medical objects; extracting first medical data and second medical data corresponding to the first clinical section and the second clinical section respectively from the plurality of medical data; analyzing the first medical data and the second medical data to obtain a plurality of first analysis results and a plurality of second analysis results; and displaying information related to the first clinical section and the second clinical section in a first display area and a second display area of the display interface respectively, wherein the information related to the first clinical section comprises at least part of a first analysis result, and the information related to the second clinical section comprises at least part of a second analysis result. The display mode of the medical data is more in line with the actual clinical requirement.

Description

Method for displaying medical data and life information processing system

Technical Field

The present invention relates to the medical field, and more particularly, to a method of displaying medical data and a vital information processing system.

Background

With the development of medical technology, various clinical data of patients are increasing. Since such data has traditionally come from different devices or systems, current medical devices or systems often organize presentation patient data by data source. Such as data from monitoring, data from treatment devices, data from care records, data from biochemical examinations, data from images, information from orders, and so forth.

However, from school study to actual clinical work, clinical staff begin to learn, and think logic is to center on the patient, recognize the patient in such a way that the system and the organ of the patient are used for analyzing and thinking about the condition of the patient. For example, consider how a person's circulatory system is, and how the circulatory system is monitored. However, if the clinical data of the patient are split, and the medical staff want to check the medical data of a certain aspect of the patient, most of the medical staff need to search the indexes needed to be checked in different devices or system software, which is very inconvenient. Especially for young doctors, it is difficult to quickly ascertain which indices are most important and most interesting from a large amount of clinical data.

Disclosure of Invention

In the summary, a series of concepts in a simplified form are introduced, which will be further described in detail in the detailed description. The summary of the invention is not intended to define the key features and essential features of the claimed subject matter, nor is it intended to be used as an aid in determining the scope of the claimed subject matter.

An embodiment of the present invention provides a method for displaying medical data, including:

obtaining a plurality of medical data of a medical subject over a preset period of time or periods from at least two medical data sources, wherein the medical data sources include: monitoring equipment, treatment equipment, examination equipment and a third party system, wherein the medical data at least comprises: monitoring data acquired from the monitoring device, treatment data acquired from the treatment device, examination data acquired from the examination device, laboratory data acquired from the third party system;

determining a plurality of clinical sections currently used, wherein the clinical sections at least comprise a first clinical section and a second clinical section, each clinical section is configured with a corresponding medical data type, the clinical section corresponds to a physiological structure of the medical object, and the physiological structure comprises a physiological system, a physiological organ, a physiological part, a tissue of the medical object, a characteristic of the physiological system or a characteristic of the physiological organ of the medical object;

Extracting first medical data and second medical data corresponding to the first clinical section and the second clinical section from the plurality of medical data according to the medical data types corresponding to the first clinical section and the second clinical section;

analyzing the first medical data to obtain a plurality of first analysis results, and analyzing the second medical data to obtain a plurality of second analysis results;

displaying information related to the first clinical section in a first display area of a display interface, and displaying information related to the second clinical section in a second display area of the display interface, wherein the information related to the first clinical section comprises at least a part of the first analysis result, and the information related to the second clinical section comprises at least a part of the second analysis result.

A second aspect of an embodiment of the present invention provides a method of displaying medical data, the method including:

obtaining a plurality of medical data for a single medical subject from at least two medical data sources, wherein the medical data sources include: monitoring device, treatment device, examination device, third party system, the medical data includes: monitoring data acquired from the monitoring device, treatment data acquired from the treatment device, examination data acquired from the examination device, laboratory data acquired from the third party system;

Determining a physiological state of the medical subject according to the medical data, wherein the physiological state at least comprises a state of a physiological structure of the medical subject, wherein the physiological structure comprises at least two physiological systems of the medical subject, the physiological systems comprise a nervous system, a circulatory system and a respiratory system, and the at least two physiological systems of the medical subject comprise a first physiological system and a second physiological system;

displaying information characterizing a physiological state of the medical subject in a display interface, the information characterizing the physiological state of the medical subject including at least information characterizing a state of a first physiological system and information characterizing a state of a second physiological system of the medical subject;

extracting first medical data corresponding to the first physiological system from the medical data, and extracting second medical data corresponding to the second physiological system from the medical data;

displaying information related to the first physiological system in a first display area of the display interface, and displaying information related to the second physiological system in a second display area of the display interface, wherein the information related to the first physiological system comprises at least a part of the first analysis result and information of overall evaluation of the first physiological system, and the information related to the second physiological system comprises at least a part of the second analysis result.

A third aspect of an embodiment of the present invention provides a method of displaying medical data, the method including:

obtaining a plurality of medical data for a single medical subject from at least two medical data sources, wherein the medical data sources include: monitoring equipment, treatment equipment, examination equipment and a third party system, wherein the medical data at least comprises: monitoring data acquired from the monitoring device, treatment data acquired from the treatment device, examination data acquired from the examination device, laboratory data acquired from the third party system;

determining at least a first clinical section and at least a second clinical section currently in use, wherein each clinical section is configured with a corresponding medical data type, the clinical section corresponding to a physiological structure of the medical subject, the physiological structure comprising a physiological system, a physiological organ, a physiological site, a tissue of the medical subject, a feature of the physiological system, or a feature of the physiological organ; extracting first medical data and second medical data corresponding to the first clinical section and the second clinical section from the plurality of medical data according to the medical data types corresponding to the first clinical section and the second clinical section;

A fourth aspect of an embodiment of the present invention provides a method of displaying medical data, the method including:

acquiring a plurality of medical data of a single medical subject, the medical data comprising at least: monitoring data acquired from the monitoring device, treatment data acquired from the treatment device, examination data acquired from the examination device, laboratory data acquired from the third party system;

displaying information related to a first portion of the medical data in a first display area of a display interface and displaying information related to a second portion of the medical data in a second display area of the display interface, wherein the first and second portions of the medical data correspond to different physiological structures of the medical subject, the physiological structures including a physiological system, a physiological organ, a physiological site, a tissue, a feature of the physiological system, or a feature of the physiological organ of the medical subject; the information related to the first portion of the medical data includes a first analysis result of analyzing the first portion of the medical data, the information related to the second portion of the medical data includes a second analysis result of analyzing the second portion of the medical data, and wherein the physiological system includes at least one of a nervous system, a circulatory system, and a respiratory system, the at least one of the first portion and the second portion of the medical data corresponding to the at least one of the nervous system, the circulatory system, and the respiratory system of the medical subject.

A fifth aspect of the embodiment of the present invention provides a vital information processing system, including a memory, a processor, and a display, where the memory is configured to store an executable program, and the processor is configured to execute the executable program, so that the processor performs the method as described above, and the processor is further configured to control the display to output a display interface.

The method for displaying the medical data and the life information processing system provided by the embodiment of the invention can be used for displaying various medical data of medical objects in a classified manner according to clinical version, and the method is more in accordance with actual clinical requirements compared with the display mode according to data sources, and different version combination templates can be selected for different medical objects or different clinical medical staff, so that the display mode of the medical data meets personalized requirements.

Drawings

The above and other objects, features and advantages of the present invention will become more apparent from the following more particular description of embodiments of the present invention, as illustrated in the accompanying drawings. The accompanying drawings are included to provide a further understanding of embodiments of the invention and are incorporated in and constitute a part of this specification, illustrate the invention and together with the embodiments of the invention, and not constitute a limitation to the invention. In the drawings, like reference numerals generally refer to like parts or steps.

FIG. 1 shows a schematic flow chart of a method of displaying medical data according to one embodiment of the invention;

FIGS. 2A and 2B illustrate schematic diagrams of display interfaces according to one embodiment of the invention;

FIGS. 3A and 3B illustrate a schematic diagram of building a layout composition template according to one embodiment of the invention;

FIG. 4 is a schematic diagram illustrating selecting a currently used layout composition template from a plurality of layout composition templates according to another embodiment of the invention;

FIG. 5 shows a schematic view of an infected print block according to one embodiment of the invention;

FIG. 6 shows a schematic view of a respiratory layout according to one embodiment of the invention;

FIG. 7 shows a schematic representation of a cardiac block according to one embodiment of the invention;

FIG. 8 shows a schematic diagram of a circulation system layout according to one embodiment of the invention;

FIG. 9 shows a schematic diagram of a nerve block according to one embodiment of the invention;

FIG. 10 shows a schematic representation of a liver layout according to one embodiment of the invention;

FIG. 11 shows a schematic view of a kidney section according to one embodiment of the invention;

FIG. 12 shows a schematic view of a coagulation block according to an embodiment of the invention;

FIG. 13 shows a schematic view of a nutrition block according to one embodiment of the invention;

FIG. 14 shows a schematic diagram of nutrient balance management according to one embodiment of the invention;

FIG. 15 shows a schematic diagram of circulating system laboratory index details, according to one embodiment of the invention;

FIG. 16 shows a schematic block diagram of a vital information processing system in accordance with one embodiment of the present invention.

Detailed Description

In order to make the objects, technical solutions and advantages of the present invention more apparent, exemplary embodiments according to the present invention will be described in detail with reference to the accompanying drawings. It should be apparent that the described embodiments are only some embodiments of the present invention and not all embodiments of the present invention, and it should be understood that the present invention is not limited by the example embodiments described herein. Based on the embodiments of the invention described in the present application, all other embodiments that a person skilled in the art would have without inventive effort shall fall within the scope of the invention.

In the following description, numerous specific details are set forth in order to provide a more thorough understanding of the present invention. It will be apparent, however, to one skilled in the art that the invention may be practiced without one or more of these details. In other instances, well-known features have not been described in detail in order to avoid obscuring the invention.

It should be understood that the present invention may be embodied in various forms and should not be construed as limited to the embodiments set forth herein. Rather, these embodiments are provided so that this disclosure will be thorough and complete, and will fully convey the scope of the invention to those skilled in the art.

The terminology used herein is for the purpose of describing particular embodiments only and is not intended to be limiting of the invention. As used herein, the singular forms "a", "an" and "the" are intended to include the plural forms as well, unless the context clearly indicates otherwise. It will be further understood that the terms "comprises" and/or "comprising," when used in this specification, specify the presence of stated features, integers, steps, operations, elements, and/or components, but do not preclude the presence or addition of one or more other features, integers, steps, operations, elements, components, and/or groups thereof. As used herein, the term "and/or" includes any and all combinations of the associated listed items.

In order to provide a thorough understanding of the present invention, detailed structures will be presented in the following description in order to illustrate the technical solutions presented by the present invention. Alternative embodiments of the invention are described in detail below, however, the invention may have other implementations in addition to these detailed descriptions.

At present, the monitoring equipment mainly adopts the following alarm methods to alarm: the alarm method based on the single vital sign data comprises the steps of alarming when the fact that the value of the single vital sign data exceeds an alarm threshold value at a preset time point or in a preset period of time is determined; secondly, an alarm method based on a plurality of vital sign data is used for alarming when the plurality of vital sign data are determined to exceed an alarm threshold value at the same time; thirdly, a trend alarming method based on single vital sign data alarms when the single vital sign data is determined to be in a descending trend or an ascending trend within a preset period of time.

However, there is often a correlation between vital sign data and other patient data, and patient status is often manifested in the combined manifestation of multiple patient data. The related relation is not considered in the alarm method of the existing monitoring equipment, so that the problems of false alarm, missing alarm and the like are easy to occur. Moreover, the existing monitoring equipment can only provide objective description of the physiological state of the patient, the interpretation of vital sign parameters depends on the experience of doctors to a great extent, doctors with relatively limited seniority easily ignore the disease deterioration implied by synchronous change of a plurality of parameters, and the diagnosis and treatment of the patient are delayed. The independent parameter monitoring cannot effectively utilize the information of a large number of vital sign parameters acquired by the monitoring equipment, and the change of the state of the patient transmitted by the vital sign parameters cannot be mined.

In addition, although related methods comprehensively analyze various vital sign parameters based on technologies such as machine learning and the like, generally due to the defects of the machine learning and the like in the current stage of the technologies, clinically unacceptable abnormal alarms are easily output, the methods generally rely on training data highly, and under the current situation that the acquisition of clinical data is difficult, the model is more difficult to perform sufficient model training, and the result output by the model is difficult to obtain the trust of clinical medical staff.

In order to overcome the above-mentioned shortcomings of the existing monitoring devices, the vital information processing system according to the embodiments of the present invention may be used to implement state monitoring. The state monitoring refers to monitoring the physiological state of a patient by integrating various medical data in one or more periods of time, and can prompt or alarm when abnormal physiological state is monitored. The physiological state of a patient is an evaluation result of the physiological function of the whole or part of the patient, and reflects the health condition of the whole or part of the patient. The subject of the state monitoring includes, but is not limited to, a physiological system, a physiological organ, a physiological site, a tissue, a feature of the physiological system or a feature of the physiological organ, etc. of the medical subject.

Compared with parameter alarm, the state monitoring is more complicated clinically, the independent vital sign data is difficult to support the determination of the state of the patient, the vital information processing system of the embodiment of the method acquires various medical data through various ways, and comprehensively analyzes the various medical data, so that the physiological state obtained by analysis is more accurate, and the situation that the wrong physiological state is obtained or the physiological state cannot be obtained due to insufficient information is avoided.

Next, a method of displaying medical data according to an embodiment of the present invention will be described with reference to fig. 1. Fig. 1 is a schematic flow chart of a method 100 of displaying medical data according to an embodiment of the invention.

As shown in fig. 1, a method 100 of displaying medical data according to an embodiment of the present invention includes the steps of:

in step S101, a plurality of medical data of a medical object for a preset period or a plurality of periods of time is acquired from at least two medical data sources, wherein the medical data sources include: monitoring equipment, treatment equipment, examination equipment and a third party system, wherein the medical data at least comprises: monitoring data acquired from the monitoring device, treatment data acquired from the treatment device, examination data acquired from the examination device, laboratory data acquired from the third party system;

In step S102, determining a plurality of clinical sections currently used, the clinical sections including at least a first clinical section and a second clinical section, wherein each clinical section is configured with a corresponding medical data type, the clinical section corresponds to a physiological structure of the medical subject, the physiological structure including a physiological system, a physiological organ, a physiological site, a tissue of the medical subject, a feature of the physiological system, or a feature of the physiological organ;

in step S103, according to the medical data types corresponding to the first clinical section and the second clinical section, extracting first medical data and second medical data corresponding to the first clinical section and the second clinical section from the plurality of medical data;

in step S104, the first medical data is analyzed to obtain a plurality of first analysis results, and the second medical data is analyzed to obtain a plurality of second analysis results;

in step S105, information related to the first clinical layout is displayed in a first display area of a display interface, and information related to the second clinical layout is displayed in a second display area of the display interface, wherein the information related to the first clinical layout includes at least a portion of the first analysis result, and the information related to the second clinical layout includes at least a portion of the second analysis result.

The method 100 for displaying medical data according to the embodiment of the invention classifies and displays various medical data of a medical object according to clinical layouts, the clinical layouts correspond to physiological structures, the clinical layouts more meet actual clinical requirements than the display modes according to data sources, and different layout combination templates can be selected for different medical objects or different clinical medical staff, so that the display modes of the medical data meet personalized requirements.

The various medical data of the medical subject may come from specific medical devices, as well as from certain medical systems, applications. In some embodiments, the data sources of the medical data include at least two of: monitoring devices, therapeutic devices, examination devices, and third party systems. Wherein, the guardianship equipment includes the monitor, and treatment equipment includes breathing machine, infusion pump, extracorporeal circulation equipment etc. and the inspection equipment includes ultrasonic imaging system, endoscope system etc. and the third party system includes PACS system (image archiving and communication system), LIS system (laboratory information system), CIS system (clinical information system) etc.. The medical data includes monitored data acquired from a monitoring device, treatment data acquired from a treatment device, examination data acquired from an examination device, laboratory data acquired from a third party system, etc., and may specifically include various physiological parameters, biochemical examination result data, image data, medical orders or case data or information, clinical assessment data or information manually entered by a user, etc.

The preset time period or periods may be a fixed time period, such as 24 hours, 48 hours, etc., or the preset time period or periods may be set by the user as shown in the dashed box of fig. 3B. By integrating and displaying the medical data for one or more periods of time, the status of the medical object can be presented more completely and comprehensively than if the real-time monitoring data were displayed alone. In particular, medical data may be selected for one or more periods of time based on the time stamp of the medical data. By way of example, if there is no medical data of a certain type for the one or more periods of time, e.g., certain laboratory test data may not have a test result within 24 hours, then the most recently acquired medical data of that type may be selected for subsequent data processing.

For example, after the medical data is acquired, the medical data may be classified to determine a clinical section corresponding to each medical data, and specifically, the medical data may be labeled according to a medical data type corresponding to the clinical section, so as to implement data classification. The clinical layout is based on the presentation mode conforming to the diagnosis and treatment habit provided by the thinking logic of clinical staff, and the multi-source data can be classified, integrated, analyzed and presented in a structured mode through the clinical layout.

When a user needs to view medical data of a medical object, an applicable layout combination template can be selected, and a plurality of clinical layouts currently used, called target clinical layouts, are selected from a plurality of clinical layouts according to the currently used layout combination template. Wherein each clinical section is configured with a corresponding medical data type, data processing rules, etc. Different clinical segments correspond to different physiological structures including a physiological system, a physiological organ, a physiological site, a tissue of a medical subject, a feature of the physiological system, or a feature of the physiological organ. Illustratively, the physiological system includes at least one of the motor system, the nervous system, the endocrine system, the circulatory system, the respiratory system, the digestive system, the urinary system, and the reproductive system; the physiological organ includes at least one of brain, heart, lung, liver, stomach, and kidney; the physiological site includes at least one of a head, a chest, and an abdomen; the tissue includes at least one of muscle tissue, nerve tissue, and epithelial tissue; characteristics of the physiological system or of the physiological organ include at least one of access, clotting, nutrition, infection, blood glucose, and medical events. Different physiological structures correspond to different clinical layouts, and users can expand and change the clinical layouts according to actual requirements. For example, a clinical block corresponding to the amount of access and a clinical block corresponding to the kidney may be combined into a clinical block corresponding to the kidney and the amount of access, or a new clinical block corresponding to sedation and analgesia may be added. The first clinical section and the second clinical section of the embodiment of the present invention may be any two clinical sections among the above-mentioned clinical sections.

For example, in the display interface of fig. 2A, the target clinical section includes a clinical section 202 corresponding to the physiological state of the patient (simply referred to as a physiological state overall evaluation section), a section 203 corresponding to infection (simply referred to as an infection section, and the like), a medical event section 213, a respiratory system section 205, a heart section 206, a circulatory system section 207, a nervous system section 208, a liver section 209, a kidney section 210, a coagulation section 211, and a nutrition section 212. In the display interface of fig. 2B, the target clinical layout includes a physiological status population assessment layout, an infection layout, a medical event layout, a respiratory system layout, a heart layout, a circulatory system layout, a nervous system layout, a liver layout, a kidney layout, and a coagulation layout. The information for the different clinical sections is presented centrally in an independent manner, e.g. one independent card for each clinical section in fig. 2A and 2B. In addition, different clinical sections can be distinguished by different colors, or distinguished by boundary lines, etc. The corresponding display of each clinical version will be described in detail below with reference to fig. 5-14.

In some embodiments, the user may create and store at least one layout combination template, i.e., in response to a user selecting at least two clinical layouts from a plurality of clinical layouts, the at least one layout combination template is created and stored, the at least one layout combination template including at least the clinical layout selected by the user. Further, the user may select a currently used layout combination template from the at least one layout combination template established by the user, that is, in response to an operation of selecting one layout combination template from the at least one layout combination template by the user, determine the selected layout combination template as the currently used layout combination template, and display information related to clinical layout included in the currently used layout combination template in the display interface.

In another embodiment, the user may also select a currently used layout combination template from a plurality of pre-stored layout combination templates, i.e., in response to a user selecting one layout combination template from the plurality of pre-stored layout combination templates, determine the selected layout combination template as the currently used layout combination template. The prestored plurality of layout block combination templates can be prestored when the equipment leaves the factory.

Illustratively, at least two of the layout composition templates include at least layout composition templates corresponding to different patient types. For example, for craniocerebral trauma patients, elderly patients, heart failure patients, extracorporeal circulation support patients, and acute respiratory distress syndrome ARDS patients, block combination templates which accord with information such as parameters, indexes and the like which need to be focused on for diagnosing and treating the patients are respectively defined. The layout combination templates can also comprise layout combination templates corresponding to different clinical medical staff, such as a cardiovascular doctor, a respiratory therapist and a rehabilitation manager, which respectively define and focus the information of parameters, indexes and the like focused by the clinical medical staff.

In addition, the medical data type corresponding to each clinical section can also be customized by a user, and the medical data type corresponding to each clinical section can be determined according to the received user instruction. Wherein, the type of medical data corresponding to the first clinical section and/or the second clinical section can be determined in response to the instruction input by the user. The user can select the clinical version to be displayed and the medical data type corresponding to the target clinical version in consideration of the symptoms (such as heart failure, injury, respiratory failure and the like), hospital equipment, hospital conditions and other factors of the patient.

FIGS. 3A and 3B provide a custom interface for a layout composition template. In this interface, the user can make changes to an existing layout composition template or create a new layout composition template. The user may select a target clinical layout constituting the current layout combination template from among the plurality of clinical layouts, and select a medical data type corresponding to each target clinical layout. For example, in FIG. 3B, for a circulatory system layout, a user may select the status indicators (i.e., core indicators), trend parameters (i.e., primary parameters), secondary parameters, and laboratory indicators that the layout displays as desired.

The customization interface adopts a visual definition concept, so that a user can obtain the information in the customization process, the clinical sections to be displayed and the information displayed by each clinical section are flexibly set, and the customization interface is convenient to operate and understand. As shown in fig. 3B, a closing icon is displayed in the upper right corner of each clinical section, and when a selection operation of the closing icon of a certain clinical section is received, the clinical section is deleted from the section combination template. Or dragging a clinical layout to a preset position in the display interface, so that the clinical layout is deleted from the layout combination template. For the currently selected clinical section, displaying all medical data corresponding to the clinical section on the right side of a display interface, and displaying a closing icon on the right side of each medical data, wherein the medical data corresponding to the closing icon can be deleted from the corresponding clinical section in response to the selection operation of the closing icon. In addition, the user may also adjust the display location, display area size (e.g., by a zoom gesture operation), etc. of each clinical section. The user may operate directly on the original display interface in a manner similar to that described above, except that the user enters the customization interface to perform customization.

Meanwhile, the layout combination template not only can be used for customizing the template of the user, but also can share or release the customized template for other people to use. In practical application, a user can conveniently select a currently used layout combination template from a plurality of layout combination templates, and the plurality of layout combination templates can be established by the current user or by other users. For example, in fig. 4, the user may select a drop-down selection box marked by a left broken line, and select a type of heart failure plate combination template from a plurality of plate combination templates provided in a drop-down menu, such as craniocerebral injury, heart failure, advanced patients, extracorporeal circulation support, postoperative patients, ARDS, and the like, so as to display a display interface suitable for the heart failure patient.

After determining the target clinical layout corresponding to the currently used layout combination template, medical data meeting the requirements is selected for each target clinical layout according to the constraint of the target clinical layout for display. Firstly, the medical data meeting the requirements is medical data of a medical data type corresponding to a target clinical edition, for example, the medical data corresponding to a respiratory system edition comprises blood oxygen saturation, respiratory rate, oxygen concentration, end-tidal carbon dioxide and the like.

Wherein, according to the medical data types corresponding to the first clinical edition and the second clinical edition, the first medical data and the second medical data respectively corresponding to the first clinical edition and the second clinical edition are extracted from the plurality of medical data, and the types of the extracted first medical data and the second medical data can be less than the medical data types fixed by the clinical edition.

In addition, after the medical data corresponding to each target clinical edition is extracted, the medical data can be filtered. Specifically, the quality analysis can be performed on the medical data, the medical data meeting the preset quality requirement is extracted, the medical data which does not meet the preset quality requirement is removed, and the medical data displayed in the display interface is the medical data meeting the preset quality requirement. In particular, the quality analysis of continuous measurement data in medical data helps to filter out data that is not of practical clinical value due to interference. The data that does not meet the preset quality requirements includes at least data that is outside of the physiological range of values due to clinical procedures of medical care. The method can remove the original medical data and also can remove the analysis result after the original medical data is processed.

And then, carrying out analysis statistics and refinement on the medical data corresponding to each target clinical edition. Specifically, analyzing the first medical data to obtain a plurality of first analysis results, and analyzing the second medical data to obtain a plurality of second analysis results; and then, displaying information related to the first clinical layout in a first display area of the display interface, and displaying information related to the second clinical layout in a second display area of the display interface, wherein the information related to the first clinical layout comprises at least part of the first analysis result, and the information related to the second clinical layout comprises at least part of the second analysis result.

In the data analysis stage, data processing is carried out on the medical data belonging to the target clinical edition, and analysis results required to be provided for users are extracted from the medical data. In some embodiments, the analysis results include at least one of: the numerical value of the medical data, the trend graph of the medical data, the target achievement of the medical data, and the analysis result obtained based on at least one medical data. The type of analysis result can be customized by the user in the customization interface, the user can select the medical data of which the numerical value needs to be displayed, the medical data of which the trend graph needs to be displayed, the medical data of which the target achievement condition needs to be displayed, and the like. The values of the medical data may include, among other things, measured values of vital sign parameters, laboratory indicators, ventilator parameters, infusion pump parameters, ultrasound measurement parameters, and the like. The change trend graph of the medical data is generated according to the medical data in a period of time, and the section of the medical data beyond the normal range can be marked on the change trend graph. The goal achievement status of the medical data may include a current goal achievement status of the medical data, i.e., an indication of whether the medical data is currently within a goal range; the goal achievement may also be a statistic of goal achievement over a period of time. The evaluation results based on the at least one medical data may include various clinical evaluation results, for example, SOFA scores may be calculated according to SOFA scoring rules. The evaluation result based on the at least one medical data may also include an identification result of the abnormal event, a statistical value of the medical data, and the like.

The analysis result obtained based on the at least one medical data may also be summarized information corresponding to the target clinical layout, and the summarized information may be a layout summary of the target clinical layout. The summary information may be obtained directly from the medical data, or may be obtained by further summary analysis of other analysis results. The summary information may be a summary of the whole section, for example, including a worsening state of an organ or system corresponding to the target clinical section, an explanatory description of the worsening state, and the like, and may also include prompt information for medical care, for example, diagnosis and treatment advice, and the like.

In some embodiments, the summarized information may include a representation of the physiological cause that caused the patient's physiological state, thereby providing the user with a deeper explanation about the patient's state. Among these, physiological causes are physiological causes that are determined based on biomedical principles, clinical experience, etc., and lead to the current patient state, and may specifically be a certain disease or injury (i.e., cause). The physiological cause may also be a patient status of another aspect, e.g. a physiological cause related to a patient status of a physiological system may be a status of a certain tissue or organ in the physiological system, e.g. a status deterioration of a certain tissue or organ leads to a deterioration of the whole system; alternatively, the physiological cause may be a state of another physiological system, e.g., a state deterioration of one physiological system results in a state deterioration of another physiological system. In summary, there is a causal relationship between physiological causes and the physiological state of the patient.

After the data processing, the medical data of each target clinical version can be displayed on the display interface. Specifically, the display interface includes a plurality of display areas, and medical data corresponding to different target clinical sections is displayed in the different display areas. The content displayed in the display interface may be refreshed according to preset rules. For example, the content displayed in the display interface may be refreshed when the user switches the display interface, or refreshed uniformly at regular intervals, or refreshed when a new laboratory test result or image test result is received, or refreshed when a critical value event or other alarm event is detected, or the like.

In some embodiments, the plurality of clinical sections may be further divided into at least a first-level clinical section and a second-level clinical section according to the importance of each clinical section; the method includes the steps of allocating a region of a first area size in a display interface for displaying a first level of clinical layout and allocating a region of a second area size for displaying a second level of clinical layout, wherein the first area is larger than the second area. That is, a larger display area is allocated for clinical sections of higher importance. In addition, the display order of the plurality of clinical sections can be set according to the importance degree of each clinical section, for example, the clinical sections with higher importance degree are displayed above the display interface or in the central area.

Further, in response to a selection instruction for the target display area, a detail area corresponding to the target display area may be displayed, and in the detail area corresponding to the target display area, detailed information of medical data related to the target clinical section corresponding to the target display area may be displayed. Wherein, in response to a selection operation of the first display area by the user, detailed information of the first analysis result of the first medical data is displayed in a third display area of the display interface, wherein the area of the third display area is larger than that of the first display area; and displaying detailed information of a second analysis result of the second medical data in a fourth display area of the display interface in response to a selection operation of the second display area by a user, wherein the area of the fourth display area is larger than that of the second display area. For example, the user may select a respiratory block to trigger the display of a detail area corresponding to the respiratory block, view more, more detailed analysis of the respiratory system, such as detailed laboratory indicators, and past time indicator history data, etc. The detail area may be in the form of a window superimposed on the original display interface, or may be a display area reassigned in the original display interface.

Referring to fig. 2A, the target clinical layout includes a medical event layout 213, and the related information of the medical event layout 213 includes medical events that occur in the course of receiving treatment or monitoring by the medical subject. Illustratively, the medical event includes at least one of: vital sign alarm events, critical value events, and medical device events. Vital sign alarm events are events in which an alarm state occurs in vital signs, critical value events are events in which critical values are identified in medical data, and medical equipment events are events recorded in the running process of treatment equipment, supporting equipment or monitoring equipment and the like.

In some embodiments, the medical events to be displayed in the medical event layout may be determined based on the received user instructions. The user can customize the type of the medical event to be focused, and after the user is customized, the display area corresponding to the medical event layout only displays the medical events occurring in the user-defined range, so that excessive unnecessary event interference is avoided.

For example, when displaying medical data corresponding to a medical event layout, a currently occurring medical event may also be displayed differently from an occurring medical event, so that a user can determine which medical events are occurring medical events and which medical events are currently occurring medical events.

The target clinical block includes a physiological state overall assessment block. Referring to fig. 5, a physiological status overall evaluation block 501 is used to display the overall evaluation result of the physiological status of the medical subject to represent the macroscopic status of the medical subject. The overall evaluation result may be a comprehensive evaluation result of the medical object under a preset evaluation criterion. The preset evaluation criteria may be selected among a variety of evaluation criteria, for example, the comprehensive evaluation result under the preset evaluation criteria may be a SOFA score for sepsis screening, an EWS score for early warning, an APACHE score for acute physiology and chronic health evaluation, and the like. The clinical user can select or customize the preset evaluation criteria for the medical object according to the actual situation of the own department. Specifically, the overall assessment of the physiological state of the medical subject is determined in accordance with at least one of: the medical system comprises a physiological system state of a medical object, a critical degree of the medical object, a disease condition type of the medical object, a stability of the physiological state of the medical object, a type of a department in which the medical object is located, a position of a ward in which the medical object is located, a hospital bed number of the medical object, a role of a medical patient's medical manager, a clinical operation performed by medical care on the medical object, information related to a level judgment of the medical object, which is input in advance by medical care, an admission time of the medical object, a type or a dose of a medicine ingested by the medical object, a heart lung state classification evaluation result of the medical object, an SOFA score of the medical object, a NEWS score of the medical object, or a score input by a user.

Illustratively, the analysis results corresponding to each clinical version include at least one of: core index, main parameter, secondary parameter and auxiliary information. Wherein, the core index reflects the core state of the clinical edition; the display content of the main parameters comprises values and a change trend graph of the main parameters; the display content of the secondary parameter comprises the numerical value of the secondary parameter; the auxiliary information includes at least one of alarm information, medical device information, and treatment means information. By displaying the medical data, the most important information or parameters which need to be focused are extracted from a large amount of clinical data and provided for clinicians, so that the clinicians can quickly master the core indexes and the important parameters and the change conditions of the important parameters of all aspects of the patients, and the core indexes and the main parameters can be selected by the senior clinicians, thereby being beneficial to realizing the transmission of the diagnosis and treatment knowledge and thought of the senior clinicians and providing guidance for young doctors.

With continued reference to fig. 5, relevant information for an infected corresponding clinical section (abbreviated as infected section, and so on) 502 includes at least one of the following: biochemical index parameters related to infection, vital sign parameters related to infection, wound status information. Wherein the biochemical marker parameters 503 associated with the infection include white blood cell count (WBC), C-reactive protein (CRP), procalcitonin (PCT), interleukin-6 (IL-6), neutral cell ratio (NEU%); vital sign parameters associated with infection include, but are not limited to, body temperature; wound status information 504 includes whether there is a pressure sore, whether there is a deep vein catheterization wound, whether there is a surgical wound, etc.

As shown in fig. 6, the core indicators 601 of the respiratory block include oxygenation index (PaO 2/FiO 2). The main parameters 602 of the respiratory block include at least one of: blood oxygen saturation (SpO 2), respiratory Rate (RR); for patients with ventilation, the main parameters also include the concentration of inhaled oxygen (FiO 2), the end-tidal carbon dioxide, and the parameters of the ventilator or oxygen therapy device, etc. For the main parameters, both the measured values of the parameters and the trend graph of the parameters are displayed. For SpO2, at least a target achievement status and a target achievement statistic result may be provided, where the target achievement status is indicated in the form of a dashboard, the dashboard is marked with a target range, the position pointed by the pointer is the current measured value, and the pointer points to the target range to indicate that the current measured value is within the target range, and the target achievement statistic structure is, for example, "a 24-hour target achievement ratio is 85%".

Secondary parameters 603 of the respiratory block include blood gas analysis parameters and/or ventilator parameters. Wherein the measured values of the blood gas analysis parameters include lactic acid (Lac), arterial oxygen partial pressure (PaO 2), arterial carbon dioxide partial pressure (PaCO 2), etc.; the measurements of ventilator parameters include tidal volume (Tv), positive End Expiratory Pressure (PEEP), and current modes of patient oxygen delivery, e.g., SIMV ventilation mode, cannula or mask, etc. For measurements that exceed the normal range, a marker may be given highlighting. Illustratively, a change between these parameters and the last measured parameter may also be provided.

Further, in response to a selection instruction of the secondary parameter, numerical values and change trend graphs of the secondary parameter in a preset time period are displayed. For secondary parameters, particularly laboratory indicators, a window may be displayed in response to user selection instructions, in which a trend graph and specific values of the parameter over a period of time are presented. Meanwhile, through dragging up and down, the trend graph and specific numerical values of other parameters related to the stimulation parameter can be checked. The user may drag the window to change its position. This is illustratively supported for secondary parameters in other clinical sections as well.

Illustratively, also displayed in the display area of the respiratory block is an entry 604 for a manual clinical assessment tool of the user, which entry 604 may be selected by the user to enable the manual clinical assessment tool. Illustratively, other clinical sections have the same icons corresponding to respective clinical assessment tool entries.

As described above, the display of the target clinical version may also include overall evaluation results, such as version nodules or system nodules, and as shown in fig. 2B, the summary information 215 of the respiratory version may include current problems with the respiratory system (transient hypoxia, intermittent compliance reduction), advice provided to the user (please consider adjusting ventilation support modes or parameters), possible risks (risk of pressure injury), and the like. Other target clinical sections may also include similar forms of section knots or different forms of section knots.

As shown in fig. 7, the core index (not shown) of the cardiac block includes cardiac related risk assessment results, such as TIMI (thrombolytic therapy for myocardial infarction) score. If the subject is assessed for GRACE (Global acute coronary syndrome registry), the core indicators of the cardiac block may also include GRACE scores.

The main parameters 701 of the cardiac block include heart rate. The display of the heart rate includes a real-time heart rate value and a trend graph over a period of time, and may also provide, for example, a target achievement of the heart rate, i.e., a situation in which a measured value reaches a target range over a period of time.

Secondary parameters 702 of the cardiac block include cardiac-related biochemical markers, such as creatine kinase isozyme (CK-MB), troponin (cTn), natriuretic titanium (NT-proBNP), and the like. For biochemical marker measurements that exceed the normal range, a marker highlighting is given. At the same time, a change between these parameters and the last measurement can also be provided.

The auxiliary information 703 of the cardiac block includes cardiac related alarm events, e.g., for severe arrhythmia events, fatal arrhythmia event information may be displayed, including the number of occurrences of arrhythmia over a period of time. The auxiliary information of the cardiac block may also include ST elevation or depression events, etc.

The circulatory system is used to provide indices and information related to hemodynamics and perfusion. As shown in fig. 8, the core index 801 of the circulatory system layout includes a shock index. The main parameters 802 of the circulatory system section at least include blood pressure, and if the medical subject is monitored for advanced hemodynamic parameters, the main parameters of the circulatory system also include cardiac output and lactic acid (Lac), and the display contents of the three include the monitored parameters and a trend graph. The blood pressure can be invasive blood pressure or noninvasive blood pressure. Meanwhile, the target range of the blood pressure can be provided to achieve the condition analysis result. For example, for main parameters of the circulatory system and other clinical sections, a selection instruction of a user for main parameters required to be subject to target management can be obtained, and target range standard statistics information can be provided according to the user selection instruction.

Secondary parameters 803 of the circulatory system include laboratory indicators and hemodynamic parameters related to hemodynamic and perfusion conditions. Among them, laboratory indicators include, but are not limited to, hemoglobin (Hb or HGB), red blood cell count (RBC), pH, HCO3, base remaining (BE); hemodynamic parameters include, but are not limited to, central venous pressure, CVP, peripheral vascular resistance index, SVRI, pulmonary water index, ELWI, and central venous oxygen saturation, scvO2. For example, for laboratory indicators with multiple measurements, change information between the last and previous test results may be presented.

The auxiliary information 804 of the circulatory system includes information of the supporting device or the therapeutic device related to the circulatory system, including a therapeutic mode used by the supporting device or the therapeutic device, key parameters of the device, and the like. For example, whether to use an external loop support device such as ECMO; whether a balloon refute pump IABP is used; whether to use vasoactive drugs, etc.

The nervous system block is used for providing indexes and information related to brain nerves. As shown in fig. 9, the core index 901 of the nervous system block includes a consciousness score, which is commonly used clinically as a GCS score (glasgo coma score), but also allows the user to define consciousness score rules by himself. The consciousness scores shown in fig. 9 include GCS scores and sub-term scores, where E represents eye movement scores, V represents speaking scores, and M represents limb activity scores.

The main parameters 902 of the nervous system section comprise brain blood pressure and blood oxygen indexes, and the display content comprises detection values and change trend graphs of the brain blood pressure and blood oxygen indexes and target achievement conditions. Secondary parameters 903 of the neural block include clinical assessment results related to the neural system, such as an assessment of pupil size, an assessment of pupil light reflex, an assessment of limb muscle strength, and the like.

The liver block is used for providing important liver indexes. As shown in fig. 10, the main parameters of the liver block include liver function evaluation index. Liver function assessment indices provided by default include alanine Aminotransferase (ALT), gamma Glutamyl Transfer (GGT), total bilirubin (Tbil), direct bilirubin (Dbil), and blood Ammonia (AMM). For the index with multiple evaluation, the change information of the latest index and the previous index is presented. The user can customize the liver function assessment index that he wishes to view. Illustratively, if the medical subject performs liver function assessment, for example, obtains a Child-pugh grading score, scoring result information is provided in a display area corresponding to the liver section.

The kidney section is used for providing main information of the kidney and information related to the input and output of the medical object. As shown in fig. 11, the core index 1101 of the kidney section includes a creatinine index. The main parameters of the kidney section include urine volume 1102, which may provide, for example, a 24 hour urine volume and an hourly urine volume change trend. Secondary parameters 1103 of the kidney section include fluid access. For example, the fluid access may be automatically obtained or manually entered by a user.

The information about the liquid input/output amount includes a liquid input amount and a liquid output amount, wherein the liquid input amount includes a total input amount for 24 hours, and a liquid input amount by an infusion pump which pumps into a human body within 24 hours. Further, the liquid intake may also include a dietary liquid amount and the like. Fluid output includes 24 hours urine, 24 hours drainage, other equipment dehydration, etc. Fluid output may also include perspiration, excretion, vomiting, bleeding fluid output, and the like.

The thrombus block is used for reflecting coagulation and bleeding of a medical object. As shown in fig. 12, the core index 1201 of the thrombus mass includes the coagulation risk evaluation result. For example, the Caprini scale may be used for coagulation risk assessment for surgical patients and the Padura scale may be used for coagulation risk assessment for non-surgical patients. In addition to providing a score and an evaluation time for coagulation risk evaluation, diagnosis and treatment advice information for the current score may also be provided. Illustratively, if the assessment is not made clinically, the coagulation risk assessment results may not be displayed.

The coagulation risk assessment results may be obtained, for example, by a third party system, or an assessment tool may be provided to obtain the coagulation risk assessment results. When providing an assessment tool, the user may be assisted in selecting an appropriate assessment scale in several ways: the first mode is that whether the operation is finished or not is obtained from a third party system, and which evaluation scale is adopted is automatically selected; the second way is to provide a user interaction interface, and determine whether the medical object is a postoperative patient according to the received user instruction, so as to automatically select which evaluation scale to use; the third group of modes is to provide a user interaction interface, and the operation user manually selects the scoring scale.

Secondary parameters of thrombus mass include coagulation index 1202 and bleeding index 1203. Wherein the coagulation index 1202 includes at least one of: activated Partial Thromboplastin Time (APTT), thrombin Time (TT), fibrinogen (Fib), D-dimer (D-dimer), fibrin Degradation Products (FDP), antithrombin III (AT-III). Bleeding indicators include Platelets (PLT), occult Blood (OB). Displaying the coagulation index 1202 and the hemorrhage index 1203 adjacent to each other in a frame helps the clinician to comprehensively evaluate both.

The nutrition edition block is used for reflecting the energy metabolism and nutrition support condition of the medical object. As shown in fig. 13, the main parameters 1302 of the nutrient block include the energy metabolism monitoring result, the secondary parameters 1303 of the nutrient block include the trace element supply amount, and the auxiliary information 1301 of the nutrient block includes the feeding mode.

The main parameters include energy metabolism value (EE) and the change trend thereof. The microelements mainly comprise calcium, iron, potassium, sodium, magnesium, etc. In addition, the nutrition supply may cause blood glucose changes, so that blood glucose measurement value information can also be provided in the display area corresponding to the nutrition block. The feeding mode mainly comprises parenteral nutrition and enteral nutrition. Wherein, the parenteral nutrition can be further divided into deep vein nutrition and superficial vein nutrition; enteral nutrition can also be subdivided into nasal feeding, gastric tubing, etc. The feeding mode may be set manually by the user.

Meanwhile, the monitored energy value and the energy value injected into the human body through the nutrition pump or the infusion pump can be subjected to energy input balance management. Daily energy intake and capacity expenditure can be counted. Wherein the energy intake may be determined based on nutritional composition information of the nutritional liquid provided to the medical subject and the amount of nutritional liquid entered. Specifically, a user firstly presets nutrition component information of used nutrition liquid, wherein the nutrition component information can be the quantity content of various energy nutrition substances in each unit liquid, and the energy substances mainly comprise fat, carbohydrate and protein; the nutritional information may also be the energy content per unit of liquid. If an energy nutrient content is used, the energy can be converted into energy by a pre-stored correspondence table of unit nutrient versus energy. The liquid amount which is accumulated and input into the body of the medical object is obtained by the nutrition supplying device, and then the energy intake of the medical object is converted by the nutrition information.

From the energy intake and the monitored energy consumption, an energy intake and output balance map as shown in fig. 14 can be drawn. Further, referring to fig. 14, a statistical map of energy intake and energy expenditure may also be displayed in response to a selection instruction for a nutrient block. Fig. 14 is only one example of an energy intake/output balance graph, and the comparison of energy intake and energy consumption may be presented by other graphical representations.

In some embodiments, when there is a significant imbalance between energy intake and energy consumption, for example, when the deviation of the two exceeds a certain threshold (e.g., 20%), an abnormality cue may also be displayed in the display area corresponding to the nutrient block, and further, a subsequent treatment recommendation may also be provided. Wherein the deviation threshold may be defined by a user.

In some embodiments, the physiological state of the medical subject may also be determined from the plurality of medical data, the physiological state including at least a state of a physiological system of the medical subject, wherein the physiological system includes at least one of a nervous system, a circulatory system, and a respiratory system of the patient. The physiological state of the medical object may be determined by matching the medical data with a pre-established rule base, finding a rule matching the medical data, and determining a physiological state corresponding to the rule. The rule base contains a large number of preset rules, the preset rules and the physiological states have a pre-established corresponding relation, the preset rules can be formulated based on various modes such as guideline rules, clinical consensus, clinical investigation and the like, and compared with the method for determining the physiological states based on a machine learning model, the method for determining the patient states according to the preset rules has higher accuracy, the determined results are more controllable, and the method is more in line with clinical cognition of medical staff. Alternatively, a variety of medical data may be input into the machine learning model resulting in the physiological state output by the machine learning model.

With continued reference to fig. 2, a human state indication map 204 may also be displayed in the display interface for indicating a physiological state of the medical subject, including but not limited to an abnormal state, which may be determined based on the data processing results or entered by a user. The human body state indication map may be a whole body map, a half body map, etc., wherein a plurality of human body organs or systems may be displayed, or only organs or systems corresponding to the target clinical version, organs or systems currently having abnormal states, or organs or systems selected by the user may be displayed.

Illustratively, the body state indication map 204 may be displayed in a central location of the display interface, with at least a portion of the display area corresponding to the target clinical version being displayed in association with a corresponding physiological structure icon in the body state indication map. The association display may include an association on the display location, e.g., a heart section adjacent to the heart location, a respiratory section adjacent to the lung location, a liver section adjacent to the liver location, etc. In some embodiments, the correspondence between the physiological structure icons and the clinical sections in the human body state indication map 204 may also be represented by lead lines.

Illustratively, the physiological state of the medical subject includes a wound state, including a wound site and/or a wound type, which may be indicated by the body state indication map 204. For example, the position corresponding to the wound site in the body state indication map 204 may be highlighted, and the wound type may be distinguished by image features such as graphics or colors, and the wound type includes pressure sores, deep veins, post-operation, and the like.

In some embodiments, the user may manipulate the body status indication map 204 to view the front, back, and left and right side wound locations of the body. If instructional information for the wound site is entered at a previous stage, the instructional information may be reviewed during the operation of the body state indication map 204.

Illustratively, the operating means may include rotating the human body state indication map 204, i.e. rotating the human body state indication map in response to a rotational operation of the human body state indication map; the manner of operation may also include expanding the body state indication map 204, i.e., in response to an expanding operation of the body state indication map, displaying views of at least two directions of the body state indication map on the same screen, e.g., simultaneously displaying the front and back surfaces.

In some embodiments, an inspection results entry control 214 is also displayed in the display interface; and when receiving an operation instruction for the examination result entry control, displaying the examination result in the medical data, wherein the examination result comprises an image examination result and/or a laboratory examination result. For example, if a new inspection result is received, a new event marker may be marked near the corresponding inspection result entry control, and event time or auxiliary information may also be displayed to prompt the user to view the newly received inspection result.

Illustratively, in addition to viewing the inspection results through the inspection results entry control 214, an inspection results identification is displayed in a display area of the target clinical layout corresponding to the inspection results through which the user may view the inspection results in addition to determining the target clinical layout corresponding to the inspection results. And when an operation instruction for identifying the inspection result is received, displaying the corresponding inspection result. For example, when a cardiac ultrasound image is received, it may be determined that it corresponds to a cardiac version and an image icon is displayed in a display area corresponding to a visceral version and the time information of the latest image is notified. The user can open the image page by clicking on the icon to view a specific static or dynamic heart ultrasound image.

In addition, in some target clinical sections, laboratory indicators may be annotated, and further, detailed information of laboratory indicators may be displayed in response to selection instructions for laboratory indicators in the target clinical sections. Referring to fig. 15, five laboratory indexes such as Hb and pH are displayed in the circulation system layout, and when a selection instruction of a display area of the laboratory indexes is received, details of the circulation system laboratory indexes including a detection result of the laboratory indexes over a period of time and a change trend graph of the detection result may be displayed in the form of a floating index, and the laboratory indexes that are too high or too low may be further marked. If laboratory indexes are included in other target clinical sections, the target clinical sections can be displayed in a floating window mode; other details of the target clinical version may also be displayed in the floating window.

In some embodiments, as shown in the dashed box of fig. 2B, a video view entry is also displayed in the display interface, where the video is captured by a video capture device, such as a camera, video camera, etc., connected to the monitoring system, typically mounted near the patient's bed, for capturing images or video data of the patient, facilitating healthcare to view the patient's state or behavior in real time, or review the patient's state or behavior over a historical period of time.

In some embodiments, a patient information unit 201 is also displayed on the display interface for providing key information of the medical object, such as name, age, gender. In addition, important supplementary information such as whether the current medical object is a postoperative patient, whether it is a patient of special interest, etc. may also be presented graphically or in text.

In summary, the method 100 for displaying medical data according to the embodiment of the present invention classifies and displays various medical data of a medical object according to clinical sections, which is more suitable for actual clinical needs than the display mode according to data sources, and can select different section combination templates for different medical objects or different clinical medical staff, so that the display mode of medical data meets personalized requirements.

Another aspect of an embodiment of the present invention provides a method of displaying medical data, the method including:

Further, a physiological state of the medical subject may also be determined from the medical data, the physiological state comprising at least a state of a physiological structure of the medical subject, wherein the physiological structure comprises at least two physiological systems of the medical subject, the physiological systems comprising a nervous system, a circulatory system, and a respiratory system, and the at least two physiological systems of the medical subject comprise a first physiological system and a second physiological system. The method further includes displaying, in a display interface, information characterizing a physiological state of the medical subject, the information characterizing the physiological state of the medical subject including at least information characterizing a state of a first physiological system and information characterizing a state of a second physiological system of the medical subject.

Wherein information of the physiological state of the medical object may be presented in the interface in a text and/or graphical manner, the graphical manner comprising at least one of an icon, a symbol, a color and a human body state indication map.

When the physiological state is presented by adopting the human body state indication map, the human body state indication map can be further rotated in response to the rotating operation of the human body state indication map; and/or, in response to the unfolding operation of the human body state indication map, displaying views of at least two directions of the human body state indication map on the same screen.

Further, the information characterizing the physiological state of the medical subject further comprises: information of an overall assessment of the physiological state of the medical subject to represent a macroscopic state of the medical subject, the overall assessment of the physiological state of the medical subject being determined in accordance with at least one of: the state of at least one physiological system of the medical subject, the criticality of the medical subject, the type of condition of the medical subject, the stability of the physiological state of the medical subject, the type of department in which the medical subject is located, the location of the ward in which the medical subject is located, the hospital bed number of the medical subject, the role of the medical subject's plumber, the role of the medical care subject the medical care performs a clinical operation on the medical subject, information related to a level judgment of the medical subject, which is input in advance by the medical care, a time of admission to the medical subject, a type or a dose of a drug taken by the medical subject, a heart lung state classification evaluation result of the medical subject, an SOFA score of the medical subject, a NEWS score of the medical subject, or a score input by a user.

Illustratively, the physiological structure of the medical subject further comprises a physiological organ, a physiological site, a tissue, a feature of the physiological system, or a feature of the physiological organ of the medical subject, the method further comprising: extracting third medical data corresponding to the physiological structure from the medical data, wherein the physiological structure comprises a physiological organ, a physiological site, a tissue, a feature of the physiological system or a feature of the physiological organ; analyzing the third medical data to obtain a plurality of third analysis results; displaying information related to a physiological organ, a physiological site, a tissue, a feature of the physiological system, or a feature of the physiological organ of the medical subject in a third display area of the display interface, the information related to the physiological organ, the physiological site, the tissue, the feature of the physiological system, or the feature of the physiological organ of the medical subject including at least a portion of the third analysis result.

In addition, the physiological system includes at least one of the motor system, endocrine system, digestive system, urinary system, and reproductive system; the physiological organ includes at least one of a brain, a heart, a lung, a liver, a stomach, and a kidney; the physiological site includes at least one of a head, a chest, and an abdomen; the tissue includes at least one of muscle tissue, nerve tissue, and epithelial tissue; the characteristic of the physiological system or the characteristic of the physiological organ includes at least one of an amount of access, coagulation, nutrition, infection, thrombosis, blood glucose, and a medical event.

For example, the type of medical data corresponding to each physiological structure may allow for customization by the user. Specifically, in response to an instruction input by a user, a type of medical data corresponding to the first physiological system and/or the second physiological system is determined.

The physiological structures included in the physiological structure combination may also allow for customization by the user. Specifically, in response to a user selecting at least two physiological structures from a plurality of physiological structures, at least one physiological structure combination including the selected at least two physiological structures is established and stored.

The user may select a currently used physiological structure combination among the at least one physiological structure combination. Wherein, in response to a user selecting one physiological structure combination from at least one physiological structure combination customized by the user, the selected physiological structure combination is determined as a currently used physiological structure combination, and information related to the physiological structure included in the currently used physiological structure combination is displayed in the display interface. Alternatively, in response to a user selecting one physiological structure combination from a plurality of physiological structure combinations stored in advance, the selected physiological structure combination may be determined as a currently used physiological structure combination, and information related to a physiological structure included in the currently used physiological structure combination may be displayed in the display interface.

In some embodiments, the user can view detailed information corresponding to each physiological structure. Specifically, in response to a user selection operation of the first display area, detailed information of the first analysis result is displayed in a fourth display area of the display interface, wherein the area of the fourth display area is larger than that of the first display area; and/or, in response to a selection operation of the second display area by a user, displaying detailed information of the second analysis result in a fifth display area of the display interface, wherein the area of the fifth display area is larger than that of the second display area.

Illustratively, the first analysis result and/or the second analysis result comprises at least one of: a core indicator, information related to a primary parameter, information related to a secondary parameter, auxiliary information, wherein the core indicator reflects a core state of a first physiological system and/or a second physiological system of the medical subject; the information related to the main parameter comprises the numerical value and the change trend graph of the main parameter; the information related to the secondary parameter includes a value of the secondary parameter; the auxiliary information comprises at least one of alarm information, medical equipment information and treatment means information.

In particular, when the physiological structure is the respiratory system of the medical subject, the core indicator comprises an oxygenation index, and the primary parameter comprises at least one of: blood oxygen saturation, respiration rate, oxygen concentration, end-tidal carbon dioxide, the secondary parameters including blood gas analysis parameters and/or ventilator parameters; when the physiological structure is a heart of the medical subject, the core indicator comprises a heart-related risk assessment, the primary parameter comprises a heart rate, the secondary parameter comprises a heart-related biochemical indicator, and the auxiliary information comprises a heart-related alarm event; when the physiological structure is the circulatory system of the medical subject, the core index comprises a shock index, the primary parameter comprises at least one of blood pressure, cardiac output and lactic acid, the secondary parameter comprises a laboratory index and a hemodynamic parameter related to hemodynamics and perfusion conditions, and the auxiliary information comprises information of a support device or a treatment device related to the circulatory system; when the physiological structure is the nervous system of the medical subject, the core metrics include a consciousness score, the primary parameters include brain blood pressure and blood oxygen metrics, and the secondary parameters include clinical assessment results related to the nervous system; when the physiological structure is the liver of the medical subject, the primary parameter includes a liver function assessment indicator; when the physiological structure is a kidney of the medical subject, the core indicator comprises a creatinine indicator, the primary parameter comprises urine volume, and the secondary parameter comprises fluid ingress and egress volume; when the physiological structure is a thrombus of the medical subject, the core index includes a coagulation risk assessment result, and the secondary parameter includes a coagulation index and a bleeding index; when the physiological structure is the nutrition of the medical object, the main parameters comprise energy metabolism monitoring results, the secondary parameters comprise trace element providing amounts, and the auxiliary information comprises feeding modes.

In some embodiments, information related to nutrition of the medical subject may be displayed in a sixth display area of the display interface; in response to a user selection operation of the sixth display area, a statistical map of an energy intake amount and an energy consumption amount is displayed, wherein the energy intake amount is determined according to nutritional composition information of the nutritional liquid supplied to the medical subject and the input nutritional liquid amount.

For more specific details regarding the method of displaying medical data, reference may be made to the relevant description of the method of displaying medical data 100, which is not described in detail herein.

Further, the method further comprises: displaying information related to a third portion of the medical data in a third display area of the display interface, and displaying information related to a fourth portion of the medical data in a fourth display area of the display interface, wherein the third and fourth portions of the medical data correspond to different physiological structures of the medical subject than the first and second portions; the information related to the third portion of the medical data includes a third analysis result obtained by analyzing the third portion of the medical data, and the information related to the fourth portion of the medical data includes a second analysis result obtained by analyzing the fourth portion of the medical data.

Illustratively, the first and second portions of the medical data correspond to two of a nervous system, a circulatory system, and a respiratory system, respectively, of the medical subject, and wherein:

on the display interface, an area of at least one of the first display region and the second display region is larger than an area of at least one of the third display region and the fourth display region; and/or the number of the groups of groups,

On the display interface, a position of at least one of the first display area and the second display area is located above a position of at least one of the third display area and the fourth display area; and/or the number of the groups of groups,

at least one of the first display area and the second display area is displayed in a more prominent manner than at least one of the third display area and the fourth display area on the display interface.

Illustratively, the physiological system further comprises at least one of a motor system, an endocrine system, a digestive system, a urinary system, and a reproductive system; the physiological organ includes at least one of a brain, a heart, a lung, a liver, a stomach, and a kidney; the physiological site includes at least one of a head, a chest, and an abdomen; the tissue includes at least one of muscle tissue, nerve tissue, and epithelial tissue; the characteristic of the physiological system or the characteristic of the physiological organ includes at least one of an amount of access, coagulation, nutrition, infection, thrombosis, blood glucose, and a medical event.

Further, the method further comprises: and displaying a human body state indication diagram in a fifth display area of the display interface, and indicating the physiological state of the medical object through the human body state indication diagram, wherein the physiological state at least comprises the state of the physiological system of the medical object.

Illustratively, a fifth display area is located in the middle of the display interface, and the first display area and the second display area are located on two sides of the fifth display area respectively.

Further, the method further comprises: displaying information characterizing a physiological state of the medical subject in a sixth display area of the display interface, the information characterizing the physiological state of the medical subject including at least information characterizing a state of at least one of a nervous system, a circulatory system, and a respiratory system of the medical subject.

Further, the method further comprises: displaying information characterizing an overall assessment of the physiological state of the medical subject in a seventh display area of the display interface to represent a macroscopic state of the medical subject, the overall assessment of the physiological state of the medical subject being determined in accordance with at least one of: the state of at least one physiological system of the medical subject, the criticality of the medical subject, the type of condition of the medical subject, the stability of the physiological state of the medical subject, the type of department in which the medical subject is located, the location of the ward in which the medical subject is located, the hospital bed number of the medical subject, the role of the medical subject's plumber, the role of the medical care subject the medical care performs a clinical operation on the medical subject, information related to a level judgment of the medical subject, which is input in advance by the medical care, a time of admission to the medical subject, a type or a dose of a drug taken by the medical subject, a heart lung state classification evaluation result of the medical subject, an SOFA score of the medical subject, a NEWS score of the medical subject, or a score input by a user.

Wherein the seventh display area may be located at an upper edge, a lower edge, a left edge, or a right edge of the display interface.

Illustratively, the medical data includes at least one of: the system comprises a core index, information related to main parameters, information related to secondary parameters and auxiliary information, wherein the core index reflects the core state of the clinical edition; the information related to the main parameter comprises the numerical value and the change trend graph of the main parameter; the information related to the secondary parameter includes a value of the secondary parameter; the auxiliary information comprises at least one of alarm information, medical equipment information and treatment means information.

When the physiological structure is the respiratory system of the medical subject, the core indicator comprises an oxygenation index, and the primary parameter comprises at least one of: blood oxygen saturation, respiration rate, oxygen concentration, end-tidal carbon dioxide, the secondary parameters including blood gas analysis parameters and/or ventilator parameters; when the physiological structure is a heart of the medical subject, the core indicator comprises a heart-related risk assessment, the primary parameter comprises a heart rate, the secondary parameter comprises a heart-related biochemical indicator, and the auxiliary information comprises a heart-related alarm event; when the physiological structure is the circulatory system of the medical subject, the core index comprises a shock index, the primary parameter comprises at least one of blood pressure, cardiac output and lactic acid, the secondary parameter comprises a laboratory index and a hemodynamic parameter related to hemodynamics and perfusion conditions, and the auxiliary information comprises information of a support device or a treatment device related to the circulatory system; when the physiological structure is the nervous system of the medical subject, the core metrics include a consciousness score, the primary parameters include brain blood pressure and blood oxygen metrics, and the secondary parameters include clinical assessment results related to the nervous system; when the physiological structure is the liver of the medical subject, the primary parameter includes a liver function assessment indicator; when the physiological structure is a kidney of the medical subject, the core indicator comprises a creatinine indicator, the primary parameter comprises urine volume, and the secondary parameter comprises fluid ingress and egress volume; when the physiological structure is a thrombus of the medical subject, the core index includes a coagulation risk assessment result, and the secondary parameter includes a coagulation index and a bleeding index; when the physiological structure is the nutrition of the medical object, the main parameters comprise energy metabolism monitoring results, the secondary parameters comprise trace element providing amounts, and the auxiliary information comprises feeding modes.

Another aspect of an embodiment of the present invention provides a method for displaying medical data, including: displaying information of a plurality of clinical sections, wherein the information of each clinical section comprises a corresponding medical data type; generating a layout combination template comprising at least two target clinical layouts of the plurality of clinical layouts according to the received selection instruction of the at least two target clinical layouts; when a display instruction of the layout combination template is received, acquiring medical data corresponding to each target clinical layout according to the type of the target medical data corresponding to each target clinical layout, and displaying the medical data corresponding to different target clinical layouts in different areas of a display interface. Based on the method for displaying the medical data, a user can customize a template for displaying the medical data according to actual needs and structurally present various medical data of a patient.

Referring to fig. 3, information for a plurality of clinical sections may be displayed in a custom interface of a section combining template, and medical data types corresponding to each clinical section may be displayed. The user can select at least two clinical sections from a plurality of clinical sections according to actual needs to form a section combination template. The selectable clinical sections include a patient status evaluation section, an infection section, a medical event section, a respiratory system section, a heart section, a circulatory system section, a nervous system section, a liver section, a kidney section, a coagulation section, and a nutrition section, and a user can select a part or all of the clinical sections as a target clinical section constituting a section combination template.

Further, in the custom interface of the layout combination template, alternative medical data types of each clinical layout may be displayed, and after selecting the target clinical layout, the user may select a target medical data type constituting the layout combination template from among a plurality of medical data types of the target clinical layout. For example, for a patient status assessment layout, the selectable medical data types include SOFA, EWS, GSC three, and the user may select SOFA as the target medical data type for which the patient status assessment layout corresponds.

Further, at the custom interface of the layout combination template, at least part of the display modes of the medical data can be displayed, and the user can select the display modes of the medical data according to the needs. The display mode of the medical data comprises numerical values, change trend graphs, target achievement conditions, evaluation results and the like.

The embodiment of the invention also provides a life information processing system for realizing the method 100 for displaying medical data. Referring to fig. 16, the vital information processing system 1600 includes a memory 1601, a processor 1602, and a display 1603; the memory 1601 is for storing various medical data of a medical subject; the processor 1602 is configured to perform the method 100 of displaying medical data described above to obtain medical data corresponding to at least two target clinical versions; the processor 1602 is further configured to control the display 1603 to display medical data corresponding to at least two target clinical tiles in the display interface, wherein medical data corresponding to different target clinical tiles are displayed in different display areas.

The vital information processing system 1600 of an embodiment of the present invention includes, but is not limited to, any one of a monitor, a local central station, a remote central station, a cloud service system, a mobile terminal, or a combination thereof. The vital information processing system may be a portable vital information processing system, a transportable vital information processing system, a mobile vital information processing system, or the like. The vital information processing system 100 may also be other devices besides a monitoring device, such as an image acquisition device, a treatment and support device, an information system (e.g., CIS, HIS, shift software, decision support system, etc.), a mobile terminal (e.g., ward).

In one embodiment, the vital information processing system 1600 may be a monitor for real-time monitoring of monitored parameters of a medical subject. The monitor is connected with other medical equipment or a third-party system through the communication module so as to acquire various medical data of the medical object. The vital information processing system 1600 may also include a central station for receiving the monitoring data transmitted by the monitors and for centrally monitoring the monitoring data. The central station connects monitors in a department or a plurality of departments through a network so as to achieve the purposes of real-time centralized monitoring and mass data storage. For example, the central station stores monitoring data, basic information of a patient, medical history information, diagnostic information, and the like, but is not limited thereto.

In some embodiments, the monitor and the central station may form an interconnection platform through a BeneLink to enable data communication between the monitor and the central station, for example, the central station may access monitoring data monitored by the monitor. In other embodiments, the monitor and the central station may also establish a data connection through a communication module including, but not limited to, wifi, bluetooth, or 2G, 3G, 4G, 5G communication modules for mobile communications.

The processor 1602 of the vital information processing system 1600 may be a central processing unit (Central Processing Unit, CPU), but may also be other general purpose processors, digital signal processors (Digital Signal Processor, DSPs), application specific integrated circuits (Application Specific Integrated Circuit, ASICs), field-programmable gate arrays (Field-Programmable Gate Array, FPGAs) or other programmable logic devices, discrete gate or transistor logic devices, discrete hardware components, or the like. A general purpose processor may be a microprocessor or the processor may be any conventional processor or the like. Processor 1602 is the control center of vital information processing system 1600 and connects the various portions of the entire vital information processing system 1600 using various interfaces and lines.

The display 1603 is used to provide visual display output to a user. In particular, the display 1603 may be used to provide a visual display interface for a user, including but not limited to a monitoring interface, a monitoring parameter setting interface, an alarm parameter setting interface, etc., and the display interface provided by the display 1603 includes at least the first display interface described above. By way of example, the display 1603 may be implemented as a touch display, or the display 1603 may have an input panel, i.e., the display 1603 may function as an input/output device.

The memory 1601 is used to store a variety of medical data for a medical subject associated with the vital information processing system 1600. The memory 1601 also stores program code, and the processor 1602 is configured to call the program code in the memory 1601 to perform steps in a display method described below. The memory 1601 may mainly include a program storage area and a data storage area, wherein the program storage area may store an operating system, application programs required for a plurality of functions, and the like. In addition, the memory 1601 may include high-speed random access memory, and may also include non-volatile memory, such as a hard disk, memory, plug-in hard disk, smart memory card, secure digital card, flash card multiple disk storage devices, flash memory devices, or other volatile solid state storage devices.

In some embodiments, vital information processing system 1600 also includes a sensor. The sensor and the processor 1602 may be coupled by a wired communication protocol or a wireless communication protocol to enable data interaction between the sensor and the processor 1602. Wireless communication techniques include, but are not limited to: various generations of mobile communication technologies (2G, 3G, 4G, and 5G), wireless networks, bluetooth (Bluetooth), zigBee, ultra wideband UWB, NFC, and the like. In particular, the sensor is used to collect monitoring data of a medical subject. Wherein the monitoring data may include, but is not limited to, one or more vital sign parameters of an electrocardiograph, respiration, pulse oximetry, heart rate, blood oxygen, non-invasive blood pressure, invasive blood pressure. In some embodiments, the sensor may be provided separately from the vital information processing system 1600 and detachably coupled to the vital information processing system 1600. The processor 1602 is also used for data processing of the monitored data signals from the sensors. In other embodiments, vital information processing system 1600 may not include a sensor, and vital information processing system 1600 may receive monitoring data collected by an external monitoring accessory via a communication module.

The vital information processing system 1600 may also include a communication module coupled to the processor 1602. In some embodiments, vital information processing system 1600 may establish data communication with other medical devices or third party devices via a communication module. The processor 1602 also controls the communication module to acquire data of the third party device or to send vital sign monitoring data acquired by the sensor to the third party device. The communication module includes, but is not limited to, a mobile communication module such as WiFI, bluetooth, NFC, zigBee, ultra wideband UWB or 2G, 3G, 4G, 5G, etc. In other embodiments, the vital information processing system 1600 may also establish a connection with a third party device via a cable.

In some embodiments, vital information processing system 1600 further includes an alarm module coupled to processor 1602 for outputting alarm prompts for a medical personnel to perform a corresponding rescue action. The alarm module includes, but is not limited to, an alarm light, an alarm speaker, etc. The alarm information may be displayed on a display, flashing through an alarm light to prompt a medical care person, or playing an alarm information through an alarm speaker, etc.

To enable user interface and data exchange, in addition to display 1603, vital information processing system 1600 may include other input/output devices connected to processor 1602, including but not limited to input devices such as a keyboard, mouse, touch screen, remote control, etc., and output devices such as printers, speakers, etc.

It should be understood that fig. 16 is merely an example of components included in the vital information processing system 1600 and is not meant to limit the vital information processing system 1600, and that the monitoring device 100 may include more components than those shown in fig. 16, or may combine certain components, or different components, e.g., the vital information processing system 1600 may further include a power module, a positioning navigation device, a printing device, etc. The method 100 of displaying medical data performed by the vital information processing system 1600 has been described above and is not further described herein. The life information processing system 1600 of the embodiment of the invention displays various medical data of medical objects according to clinical layouts in a classified manner, which is more in accordance with actual clinical requirements than the display mode according to data sources, and can select different layout combination templates for different medical objects or different clinical medical staff so that the display mode of the medical data meets personalized requirements.

Furthermore, according to an embodiment of the present invention, there is also provided a storage medium on which program instructions are stored, which program instructions, when executed by a computer or processor, are adapted to carry out the respective steps of the method of displaying medical data of an embodiment of the present invention. The storage medium may include, for example, a memory card of a smart phone, a memory component of a tablet computer, a hard disk of a personal computer, read-only memory (ROM), erasable programmable read-only memory (EPROM), portable compact disc read-only memory (CD-ROM), USB memory, or any combination of the foregoing storage media. The computer-readable storage medium may be any combination of one or more computer-readable storage media.

Although the illustrative embodiments have been described herein with reference to the accompanying drawings, it is to be understood that the above illustrative embodiments are merely illustrative and are not intended to limit the scope of the present invention thereto. Various changes and modifications may be made therein by one of ordinary skill in the art without departing from the scope and spirit of the invention. All such changes and modifications are intended to be included within the scope of the present invention as set forth in the appended claims.

Those of ordinary skill in the art will appreciate that the various illustrative elements and algorithm steps described in connection with the embodiments disclosed herein may be implemented as electronic hardware, or combinations of computer software and electronic hardware. Whether such functionality is implemented as hardware or software depends upon the particular application and design constraints imposed on the solution. Skilled artisans may implement the described functionality in varying ways for each particular application, but such implementation decisions should not be interpreted as causing a departure from the scope of the present invention.

In the several embodiments provided by the present invention, it should be understood that the disclosed apparatus and method may be implemented in other ways. For example, the above-described device embodiments are merely illustrative, e.g., the division of the elements is merely a logical functional division, and there may be additional divisions when actually implemented, e.g., multiple elements or components may be combined or integrated into another device, or some features may be omitted or not performed.

In the description provided herein, numerous specific details are set forth. However, it is understood that embodiments of the invention may be practiced without these specific details. In some instances, well-known methods, structures and techniques have not been shown in detail in order not to obscure an understanding of this description.

Similarly, it should be appreciated that in order to streamline the invention and aid in understanding one or more of the various inventive aspects, various features of the invention are sometimes grouped together in a single embodiment, figure, or description thereof in the description of exemplary embodiments of the invention. However, the method of the present invention should not be construed as reflecting the following intent: i.e., the claimed invention requires more features than are expressly recited in each claim. Rather, as the following claims reflect, inventive aspects lie in less than all features of a single disclosed embodiment. Thus, the claims following the detailed description are hereby expressly incorporated into this detailed description, with each claim standing on its own as a separate embodiment of this invention.

It will be understood by those skilled in the art that all of the features disclosed in this specification (including any accompanying claims, abstract and drawings), and all of the processes or units of any method or apparatus so disclosed, may be combined in any combination, except combinations where the features are mutually exclusive. Each feature disclosed in this specification (including any accompanying claims, abstract and drawings), may be replaced by alternative features serving the same, equivalent or similar purpose, unless expressly stated otherwise.

Furthermore, those skilled in the art will appreciate that while some embodiments described herein include some features but not others included in other embodiments, combinations of features of different embodiments are meant to be within the scope of the invention and form different embodiments. For example, in the claims, any of the claimed embodiments may be used in any combination.

Various component embodiments of the invention may be implemented in hardware, or in software modules running on one or more processors, or in a combination thereof. Those skilled in the art will appreciate that some or all of the functions of some of the modules according to embodiments of the present invention may be implemented in practice using a microprocessor or Digital Signal Processor (DSP). The present invention can also be implemented as an apparatus program (e.g., a computer program and a computer program product) for performing a portion or all of the methods described herein. Such a program embodying the present invention may be stored on a computer readable medium, or may have the form of one or more signals. Such signals may be downloaded from an internet website, provided on a carrier signal, or provided in any other form.

It should be noted that the above-mentioned embodiments illustrate rather than limit the invention, and that those skilled in the art will be able to design alternative embodiments without departing from the scope of the appended claims. In the claims, any reference signs placed between parentheses shall not be construed as limiting the claim. The invention may be implemented by means of hardware comprising several distinct elements, and by means of a suitably programmed computer. In the unit claims enumerating several means, several of these means may be embodied by one and the same item of hardware. The use of the words first, second, third, etc. do not denote any order. These words may be interpreted as names.

The foregoing description is merely illustrative of specific embodiments of the present invention and the scope of the present invention is not limited thereto, and any person skilled in the art can easily think about variations or substitutions within the scope of the present invention. The protection scope of the invention is subject to the protection scope of the claims.

Claims

1. A method of displaying medical data, the method comprising:

2. The method of claim 1, wherein the information related to the first clinical layout further comprises summarized information of the first clinical layout.

3. The method as recited in claim 1, further comprising:

dividing the plurality of clinical sections into at least a first-level clinical section and a second-level clinical section according to the importance degree of each clinical section;

allocating a first area-sized region in the display interface for displaying the first level of clinical sections and a second area-sized region for displaying the second level of clinical sections, wherein the first area is larger than the second area;

And/or setting the display sequence of the plurality of clinical sections according to the importance degree of each clinical section.

4. The method of claim 3, wherein the first grade clinical trial includes at least one of a heart, a respiratory system, a circulatory system, a nervous system,

the second grade clinical section includes at least one of locomotor system, endocrine system, digestive system, urinary system, reproductive system, brain, lung, liver, stomach, kidney, head, chest, abdomen, muscle tissue, nerve tissue, epithelial tissue, access, clotting, nutrition, infection, blood glucose, and medical event.

5. The method of claim 1, wherein the display interface is further configured to display an overall assessment of the physiological state of the medical subject to reflect a macroscopic state of the medical subject, the overall assessment of the physiological state of the medical subject being determined in accordance with at least one of: the medical system comprises a physiological system state of the medical object, a criticality of the medical object, a disease type of the medical object, a stability of the physiological state of the medical object, a type of a department in which the medical object is located, a location of a ward in which the medical object is located, a hospital bed number of the medical object, a role of a medical doctor of the medical object, a clinical operation performed by a medical care on the medical object, information related to a level judgment of the medical object, which is input in advance by the medical care, an admission time of the medical object, a type or a dose of a medicine ingested by the medical object, a heart lung state classification evaluation result of the medical object, an SOFA score of the medical object, a NEWS score of the medical object, or a score input by a user.

6. The method of claim 1, wherein the physiological system comprises at least one of the motor system, the nervous system, the endocrine system, the circulatory system, the respiratory system, the digestive system, the urinary system, and the reproductive system; the physiological organ includes at least one of a brain, a heart, a lung, a liver, a stomach, and a kidney; the physiological site includes at least one of a head, a chest, and an abdomen; the tissue includes at least one of muscle tissue, nerve tissue, and epithelial tissue; the characteristic of the physiological system or the characteristic of the physiological organ includes at least one of an amount of access, coagulation, nutrition, infection, blood glucose, and a medical event.

7. The method as recited in claim 1, further comprising: and determining the medical data type corresponding to the first clinical edition and/or the second clinical edition according to the received user instruction.

8. The method of claim 1, wherein the clinical block is further configured with a display mode of each of the medical data, the display mode including displaying a numerical value of the medical data, a trend chart, a goal achievement status, an evaluation result for the medical data.

9. The method as recited in claim 1, further comprising:

receiving user input selecting at least two clinical sections from the plurality of clinical sections;

and establishing and storing at least one layout combination template according to the received user instruction, wherein the at least one layout combination template comprises the selected at least two clinical layouts.

10. The method as recited in claim 1, further comprising:

receiving operation of selecting one plate combination template from a plurality of plate combination templates, which is input by a user;

and determining the layout combination template selected by the user as the currently used layout combination template.

11. The method according to claim 1, wherein the method further comprises:

dragging the target clinical layout to a preset position in the display interface, and canceling to display the target clinical layout;

and/or displaying a closing icon in at least part of the clinical sections, and canceling the display of the target clinical sections when the selection operation of the closing icon of the target clinical sections is received.

12. The method according to claim 1, wherein the method further comprises:

And carrying out quality analysis on the medical data, and removing the medical data which does not meet the preset quality requirement, wherein the data which does not meet the preset quality requirement at least comprises data which is beyond the physiological value range and is generated by clinical operation of medical care.

13. The method as recited in claim 1, further comprising: responding to a selection instruction of a user on the first display area, and displaying detailed information of the first analysis result of the first medical data in a third display area of the display interface, wherein the area of the third display area is larger than that of the first display area; and/or the number of the groups of groups,

and responding to a selection instruction of a user on the second display area, and displaying detailed information of the second analysis result of the second medical data in a fourth display area of the display interface, wherein the area of the fourth display area is larger than that of the second display area.

14. The method according to claim 1, wherein the method further comprises:

determining a physiological state of the medical subject from the plurality of medical data, the physiological state including at least a state of a physiological system of the medical subject, wherein the physiological system includes at least one of a nervous system, a circulatory system, and a respiratory system of the patient;

And displaying a human body state indication diagram in the display interface, and indicating the physiological state of the medical object through the human body state indication diagram, wherein the physiological state at least comprises the state of the physiological system of the medical object.

15. The method of claim 14, wherein the body state indication map is displayed in a central location of the display interface, the first display area of the first clinical section and/or the second display area of the second clinical section being displayed in association with an icon of a corresponding physiological structure in the body state indication map.

16. The method of claim 14, wherein the physiological state further comprises a wound state comprising a wound site and/or a wound type; the indicating the physiological state of the medical object through the human body state indication map further comprises:

the wound site and/or the wound type is indicated by the human body status indication map.

17. The method of claim 14, wherein the method further comprises:

rotating the human body state indication map in response to a rotation operation on the human body state indication map;

And/or, in response to an unfolding operation of the human body state indication map, displaying views of at least two directions of the human body state indication map on a same screen.

18. The method as recited in claim 1, further comprising:

displaying an inspection result entry control in the display interface;

and when an operation instruction of the examination result entry control is received, displaying examination data and/or laboratory data in the medical data.

19. The method according to claim 1, wherein the method further comprises:

determining a target clinical version corresponding to the examination data or laboratory data in the medical data;

displaying an inspection result identifier in a display area of the target clinical version;

and when an operation instruction for identifying the inspection data is received, displaying the inspection data or laboratory data.

20. The method of claim 6, wherein the method further comprises: determining a medical event to be displayed in a clinical edition corresponding to the medical event according to the received user instruction, wherein the medical event comprises at least one of the following: vital sign alarm events, critical value events, and medical device events.

21. The method of claim 6, wherein displaying the medical event comprises: the medical event that is currently occurring is displayed differently from the medical event that has occurred.

22. The method of claim 1, wherein the first analysis result and/or the second analysis result comprises at least one of: the system comprises a core index, a main parameter, a secondary parameter and auxiliary information, wherein the core index reflects the core state of the clinical edition; the display content of the main parameters comprises numerical values and change trend graphs of the main parameters; the display content of the secondary parameter comprises the numerical value of the secondary parameter; the auxiliary information comprises at least one of alarm information, medical equipment information and treatment means information.

23. The method of claim 22, wherein the method further comprises:

and responding to the selection instruction of the secondary parameter, and displaying the numerical value and the change trend graph of the secondary parameter in a preset time period.

24. The method of claim 22, wherein the core indicator comprises an oxygenation index when the first clinical block or the second clinical block corresponds to the respiratory system of the medical subject, the primary parameter comprising at least one of: blood oxygen saturation, respiration rate, oxygen concentration, end-tidal carbon dioxide, the secondary parameters including blood gas analysis parameters and/or ventilator parameters;

When the first clinical section or the second clinical section corresponds to the heart of the medical subject, the core indicator comprises a heart-related risk assessment result, the primary parameter comprises a heart rate, the secondary parameter comprises a heart-related biochemical indicator, and the auxiliary information comprises a heart-related alarm event; when the first clinical section or the second clinical section corresponds to a circulatory system section of the medical subject, the core index includes a shock index; the primary parameters include at least one of blood pressure, cardiac output, and lactic acid; the secondary parameters include laboratory indicators and hemodynamic parameters related to hemodynamic and perfusion conditions; the auxiliary information includes information of a support device or a treatment device related to the circulatory system; when the first clinical trial or the second clinical trial corresponds to the nervous system of the medical subject, the core indicators include a consciousness score; the main parameters comprise brain blood pressure and blood oxygen index; the secondary parameters include clinical assessment results related to the nervous system; when the first clinical section or the second clinical section corresponds to the liver of the medical subject, the main parameters include a liver function evaluation index; when the first clinical section or the second clinical section corresponds to the kidney of the medical subject, the core index includes a creatinine index; the primary parameter includes urine volume; the secondary parameter includes a liquid ingress and egress amount; when the first clinical section or the second clinical section corresponds to thrombus of the medical object, the core index comprises a coagulation risk assessment result, the secondary parameters comprise a coagulation index and a bleeding index, when the first clinical section or the second clinical section corresponds to nutrition of the medical object, the primary parameters comprise an energy metabolism monitoring result, the secondary parameters comprise trace element supply amount, and the auxiliary information comprises a feeding mode;

When the first clinical section or the second clinical section corresponds to the infection of the medical subject, the main parameters include biochemical index parameters related to the infection, vital sign parameters related to the infection, and wound status information.

25. The method as recited in claim 24, further comprising:

in response to a selection instruction to a display area corresponding to nutrition, a statistical map of energy intake and energy consumption is displayed, the energy intake being determined from nutritional composition information of a nutritional liquid provided to the medical subject and an input nutritional liquid amount.

26. A method of displaying medical data, the method comprising:

27. The method of claim 26, wherein the information of the physiological state of the medical object is presented in the display interface in a textual and/or graphical manner, the graphical manner including at least one of an icon, a symbol, a color, and a human state indication map.

28. The method of claim 27, wherein the method further comprises:

rotating the human body state indication map in response to a rotation operation of the human body state indication map;

29. The method of any one of claims 26 to 28, wherein the information characterizing the physiological state of the medical subject further comprises: information of an overall assessment of the physiological state of the medical subject to represent a macroscopic state of the medical subject, the overall assessment of the physiological state of the medical subject being determined in accordance with at least one of: the state of at least one physiological system of the medical subject, the criticality of the medical subject, the type of condition of the medical subject, the stability of the physiological state of the medical subject, the type of department in which the medical subject is located, the location of the ward in which the medical subject is located, the hospital bed number of the medical subject, the role of the medical subject's plumber, the role of the medical care subject the medical care performs a clinical operation on the medical subject, information related to a level judgment of the medical subject, which is input in advance by the medical care, a time of admission to the medical subject, a type or a dose of a drug taken by the medical subject, a heart lung state classification evaluation result of the medical subject, an SOFA score of the medical subject, a NEWS score of the medical subject, or a score input by a user.

30. The method of any one of claims 26 to 29, wherein the physiological structure further comprises a physiological organ, a physiological site, a tissue, a feature of the physiological system, or a feature of the physiological organ of the medical subject, the method further comprising:

extracting third medical data corresponding to the physiological structure from the medical data, wherein the physiological structure comprises a physiological organ, a physiological site, a tissue, a feature of the physiological system or a feature of the physiological organ;

analyzing the third medical data to obtain a plurality of third analysis results;

displaying information related to a physiological organ, a physiological site, a tissue, a feature of the physiological system, or a feature of the physiological organ of the medical subject in a third display area of the display interface, the information related to the physiological organ, the physiological site, the tissue, the feature of the physiological system, or the feature of the physiological organ of the medical subject including at least a portion of the third analysis result.

31. The method of claim 30, wherein the physiological system further comprises at least one of a motor system, an endocrine system, a digestive system, a urinary system, and a reproductive system; the physiological organ includes at least one of a brain, a heart, a lung, a liver, a stomach, and a kidney; the physiological site includes at least one of a head, a chest, and an abdomen; the tissue includes at least one of muscle tissue, nerve tissue, and epithelial tissue; the characteristic of the physiological system or the characteristic of the physiological organ includes at least one of an amount of access, coagulation, nutrition, infection, thrombosis, blood glucose, and a medical event.

32. The method according to any one of claims 26 to 31, further comprising: and responding to the instruction input by the user, and determining the type of medical data corresponding to the first physiological system and/or the second physiological system.

33. The method according to any one of claims 26 to 32, further comprising:

in response to a user selecting at least two physiological structures from a plurality of physiological structures, at least one physiological structure combination is established and stored, the at least one physiological structure combination including the selected at least two physiological structures.

34. The method of claim 33, wherein the method further comprises:

in response to a user selecting one physiological structure combination from the at least one physiological structure combination, determining the selected physiological structure combination as a currently used physiological structure combination, and displaying information related to physiological structures included in the currently used physiological structure combination in the display interface.

35. The method according to any one of claims 26-34, further comprising:

in response to a user selecting one physiological structure combination from a plurality of pre-stored physiological structure combinations, determining the selected physiological structure combination as a currently used physiological structure combination, and displaying information related to physiological structures included in the currently used physiological structure combination in the display interface.

36. The method according to any one of claims 26 to 35, further comprising:

responding to the selection operation of the user on the first display area, and displaying detailed information of the first analysis result in a fourth display area of the display interface, wherein the area of the fourth display area is larger than that of the first display area; and/or the number of the groups of groups,

and responding to the selection operation of the user on the second display area, and displaying the detailed information of the second analysis result in a fifth display area of the display interface, wherein the area of the fifth display area is larger than that of the second display area.

37. The method of any one of claims 26 to 26, wherein the first analysis result and/or the second analysis result comprises at least one of: a core indicator, information related to a primary parameter, information related to a secondary parameter, auxiliary information, wherein the core indicator reflects a core state of a first physiological system and/or a second physiological system of the medical subject; the information related to the main parameter comprises the numerical value and the change trend graph of the main parameter; the information related to the secondary parameter includes a value of the secondary parameter; the auxiliary information comprises at least one of alarm information, medical equipment information and treatment means information.

38. The method of claim 37, wherein when the physiological structure is the respiratory system of the medical subject, the core indicator comprises an oxygenation index and the primary parameter comprises at least one of: blood oxygen saturation, respiration rate, oxygen concentration, end-tidal carbon dioxide, the secondary parameters including blood gas analysis parameters and/or ventilator parameters;

when the physiological structure is a heart of the medical subject, the core indicator comprises a heart-related risk assessment, the primary parameter comprises a heart rate, the secondary parameter comprises a heart-related biochemical indicator, and the auxiliary information comprises a heart-related alarm event;

when the physiological structure is the circulatory system of the medical subject, the core index comprises a shock index, the primary parameter comprises at least one of blood pressure, cardiac output and lactic acid, the secondary parameter comprises a laboratory index and a hemodynamic parameter related to hemodynamics and perfusion conditions, and the auxiliary information comprises information of a support device or a treatment device related to the circulatory system;

when the physiological structure is the nervous system of the medical subject, the core metrics include a consciousness score, the primary parameters include brain blood pressure and blood oxygen metrics, and the secondary parameters include clinical assessment results related to the nervous system;

When the physiological structure is the liver of the medical subject, the primary parameter includes a liver function assessment indicator;

when the physiological structure is a kidney of the medical subject, the core indicator comprises a creatinine indicator, the primary parameter comprises urine volume, and the secondary parameter comprises fluid ingress and egress volume;

when the physiological structure is a thrombus of the medical subject, the core index includes a coagulation risk assessment result, and the secondary parameter includes a coagulation index and a bleeding index;

when the physiological structure is the nutrition of the medical object, the main parameters comprise energy metabolism monitoring results, the secondary parameters comprise trace element providing amounts, and the auxiliary information comprises feeding modes.

39. The method of claim 38, wherein the method further comprises:

displaying information related to nutrition of the medical subject in a sixth display area of the display interface;

in response to a user selection operation of the sixth display area, a statistical map of an energy intake amount and an energy consumption amount is displayed, wherein the energy intake amount is determined according to nutritional composition information of the nutritional liquid supplied to the medical subject and the input nutritional liquid amount.

40. A method of displaying medical data, the method comprising:

41. The method as recited in claim 40, further comprising:

determining a physiological state of the medical subject from the medical data, the physiological state including at least a state of a physiological system of the medical subject, wherein the physiological system includes at least two of a nervous system, a circulatory system, and a respiratory system;

displaying information characterizing the physiological state of the medical subject in the display interface, the information characterizing the physiological state of the medical subject including at least information characterizing the state of a first physiological system and information characterizing the state of a second physiological system of the medical subject.

42. The method of claim 41, wherein the information of the physiological state of the medical object is presented in the display interface in a textual and/or graphical manner, the graphical manner including at least one of an icon, a symbol, a color, and a human state indication map.

43. The method of any one of claims 40 to 42, wherein the display interface is further configured to display information of an overall assessment of the physiological state of the medical subject to represent a macroscopic state of the patient, the overall assessment of the physiological state of the medical subject being determined in accordance with at least one of: the medical system comprises a physiological system state of the medical object, a criticality of the medical object, a disease type of the medical object, a stability of the physiological state of the medical object, a type of a department in which the medical object is located, a location of a ward in which the medical object is located, a hospital bed number of the medical object, a role of a medical doctor of the medical object, a clinical operation performed by a medical care on the medical object, information related to a level judgment of the medical object, which is input in advance by the medical care, an admission time of the medical object, a type or a dose of a medicine ingested by the medical object, a heart lung state classification evaluation result of the medical object, an SOFA score of the medical object, a NEWS score of the medical object, or a score input by a user.

44. The method of any one of claims 40 to 43, wherein the physiological system comprises at least one of the motor system, the nervous system, the endocrine system, the circulatory system, the respiratory system, the digestive system, the urinary system, and the reproductive system; the physiological organ includes at least one of a brain, a heart, a lung, a liver, a stomach, and a kidney; the physiological site includes at least one of a head, a chest, and an abdomen; the tissue includes at least one of muscle tissue, nerve tissue, and epithelial tissue; the characteristic of the physiological system or the characteristic of the physiological organ includes at least one of an amount of access, coagulation, nutrition, infection, thrombosis, blood glucose, and a medical event.

45. The method of any one of claims 40, 44, further comprising: and responding to an instruction input by a user, and determining the medical data type corresponding to the first clinical section and/or the second clinical section.

46. The method of any one of claims 40 to 45, wherein the clinical block is further configured with a display of each of the medical data, the display including displaying a numerical value of the medical data, a trend graph, a goal achievement status, an evaluation result for the medical data.

47. The method of any one of claims 40 to 46, further comprising:

in response to a user selecting at least two clinical sections, at least one section combination template is created and stored, the at least one section combination template including the selected at least two clinical sections.

48. The method as recited in claim 47, further comprising:

and in response to a user selecting one of the at least one layout combination template, determining the selected layout combination template as the currently used layout combination template.

49. The method of any one of claims 40-48, further comprising:

and responding to the operation of selecting one plate combination template from a plurality of plate combination templates prestored by a user, and determining the selected plate combination template as the currently used plate combination template.

50. The method of any one of claims 40 to 49, further comprising: in response to a selection operation of the first display area by a user, displaying detailed information of the first analysis result of the first medical data in a third display area of the display interface, wherein the area of the third display area is larger than that of the first display area; and/or the number of the groups of groups,

51. The method of any one of claims 40 to 50, wherein the first analysis result and/or the second analysis result comprises at least one of: the system comprises a core index, information related to main parameters, information related to secondary parameters and auxiliary information, wherein the core index reflects the core state of the clinical edition; the information related to the main parameter comprises the numerical value and the change trend graph of the main parameter; the information related to the secondary parameter includes a value of the secondary parameter; the auxiliary information comprises at least one of alarm information, medical equipment information and treatment means information.

52. The method of claim 51, wherein when the physiological structure is the respiratory system of the medical subject, the core indicator comprises an oxygenation index and the primary parameter comprises at least one of: blood oxygen saturation, respiration rate, oxygen concentration, end-tidal carbon dioxide, the secondary parameters including blood gas analysis parameters and/or ventilator parameters;

53. A method of displaying medical data, the method comprising:

54. The method of claim 53, wherein the method further comprises:

displaying information related to a third portion of the medical data in a third display area of the display interface, and displaying information related to a fourth portion of the medical data in a fourth display area of the display interface, wherein the third and fourth portions of the medical data correspond to different physiological structures of the medical subject than the first and second portions; the information related to the third portion of the medical data includes a third analysis result obtained by analyzing the third portion of the medical data, and the information related to the fourth portion of the medical data includes a second analysis result obtained by analyzing the fourth portion of the medical data.

55. The method of claim 54, wherein the first portion and the second portion of the medical data correspond to two of a nervous system, a circulatory system, and a respiratory system, respectively, of the medical subject, and wherein:

56. The method of claim 55, wherein the physiological system further comprises at least one of a motor system, an endocrine system, a digestive system, a urinary system, and a reproductive system; the physiological organ includes at least one of a brain, a heart, a lung, a liver, a stomach, and a kidney; the physiological site includes at least one of a head, a chest, and an abdomen; the tissue includes at least one of muscle tissue, nerve tissue, and epithelial tissue; the characteristic of the physiological system or the characteristic of the physiological organ includes at least one of an amount of access, coagulation, nutrition, infection, thrombosis, blood glucose, and a medical event.

57. The method of any one of claims 53 to 56, further comprising:

And displaying a human body state indication diagram in a fifth display area of the display interface, and indicating the physiological state of the medical object through the human body state indication diagram, wherein the physiological state at least comprises the state of the physiological system of the medical object.

58. The method of claim 57, wherein the fifth display area is located in the middle of the display interface, and the first display area and the second display area are located on opposite sides of the fifth display area, respectively.

59. The method of any one of claims 53 to 58, wherein the method further comprises:

displaying information characterizing a physiological state of the medical subject in a sixth display area of the display interface, the information characterizing the physiological state of the medical subject including at least information characterizing a state of at least one of a nervous system, a circulatory system, and a respiratory system of the medical subject.

60. The method of any one of claims 53 to 59, wherein the method further comprises:

displaying information characterizing an overall assessment of the physiological state of the medical subject in a seventh display area of the display interface to represent a macroscopic state of the medical subject, the overall assessment of the physiological state of the medical subject being determined in accordance with at least one of: the state of at least one physiological system of the medical subject, the criticality of the medical subject, the type of condition of the medical subject, the stability of the physiological state of the medical subject, the type of department in which the medical subject is located, the location of the ward in which the medical subject is located, the hospital bed number of the medical subject, the role of the medical subject's plumber, the role of the medical care subject the medical care performs a clinical operation on the medical subject, information related to a level judgment of the medical subject, which is input in advance by the medical care, a time of admission to the medical subject, a type or a dose of a drug taken by the medical subject, a heart lung state classification evaluation result of the medical subject, an SOFA score of the medical subject, a NEWS score of the medical subject, or a score input by a user.

61. The method of claim 60, wherein the seventh display area is located at an upper edge, a lower edge, a left edge, or a right edge of the display interface.

62. The method of any one of claims 53-61, the medical data comprising at least one of: the system comprises a core index, information related to main parameters, information related to secondary parameters and auxiliary information, wherein the core index reflects the core state of the clinical edition; the information related to the main parameter comprises the numerical value and the change trend graph of the main parameter; the information related to the secondary parameter includes a value of the secondary parameter; the auxiliary information comprises at least one of alarm information, medical equipment information and treatment means information.

63. The method of claim 62, wherein when the physiological structure is the respiratory system of the medical subject, the core indicator comprises an oxygenation index and the primary parameter comprises at least one of: blood oxygen saturation, respiration rate, oxygen concentration, end-tidal carbon dioxide, the secondary parameters including blood gas analysis parameters and/or ventilator parameters;

64. A vital information processing system comprising a memory for storing an executable program, a processor for executing the executable program such that the processor performs the method of any one of claims 1-63, and a display for controlling the display to output a display interface.