WO2019161608A1 - Multi-parameter monitoring data analysis method and multi-parameter monitoring system - Google Patents

Abstract

A multi-parameter monitoring data analysis method and a monitoring system (1, 2). Said method comprises: acquiring sign monitoring data of a monitored object (110); performing wave group feature recognition on the acquired electrocardiographic data, performing heart beat classification on the electrocardiographic data, obtaining heart beat classification information in combination with electrocardiographic basic rule reference data, and generating electrocardiographic event data (120); determining corresponding electrocardiographic event information according to the electrocardiographic event data, and determining whether the electrocardiographic event information is electrocardiographic abnormal event information (130); outputting first alarm information if the electrocardiographic event information is electrocardiographic abnormal event information (140); and determining whether one or more of the acquired pulse data, blood pressure data, respiration data, blood oxygen saturation data and body temperature data are abnormal data which exceeds a corresponding set threshold(150); generating other abnormal event information according to the abnormal data, and outputting second alarm information if the set threshold is exceeded (160); and sending the first alarm information and/or the second alarm information to a workstation (170).

Description

Multi-parameter monitoring data analysis method and multi-parameter monitoring system

This application claims priority to Chinese Patent Application No. 201101157364.9, entitled "Multi-Parameter Monitoring Data Analysis Method and Multi-Parameter Monitoring System", filed on February 24, 2018.

Technical field

The present invention relates to the field of data processing technologies, and in particular, to a multi-parameter monitoring data analysis method and a multi-parameter monitoring system.

Background technique

A multi-parameter monitor is a commonly used clinical medical device. This monitoring device features multiple sets of sensors that can simultaneously monitor vital signs such as ECG, blood pressure, blood oxygen, pulse, respiration, and body temperature. In the ward monitoring, the multi-parameter monitor can become an important reference for the doctor to monitor the patient, so that the doctor can find the patient's problems in time and deal with it in time, thus ensuring the patient's life safety. The clinical application of the monitor can be found in: surgery, post-operative, trauma care, coronary heart disease, critically ill patients, neonates, premature infants, hyperbaric oxygen chambers, delivery rooms, etc.

In a hospital bedside monitoring system, there are often multiple multi-parameter bedside monitors in one system for monitoring multiple patient personnel. The most common application scenario is that when the bedside monitor has an alarm, the nurse station will generate an alarm message for the corresponding bed number to inform the multi-parameter monitor that the abnormality has occurred and remind the medical staff to handle it. Medical staff need to go to the patient's bed to get abnormal information, and can't get alarm messages and data in time. It is impossible to predict the abnormality and urgency, which is easy to cause delay in emergency handling.

In addition, most multi-parameter monitors on the market use a threshold setting to trigger an alarm event. For example, when the heart rate is too fast, an alarm is issued or when the heart rate is too slow. Although the method of setting the threshold is simple and intuitive, the accuracy is relatively poor, because the electrocardiographic signal is a weak current reflected by the electrical activity of the cardiomyocytes on the body surface, and is recorded by the body surface electrode and the amplified recording system. Other non-cardiogenic electrical signals, such as EMG signal interference caused by skeletal muscle activity, are also recorded during the recording process. These signals can cause incorrect heartbeat signal detection, which can trigger an alarm. These frequent false positives, over time, cause patients and medical staff to relax their vigilance against alarm events, and patients do not receive effective attention and treatment in the event of a real need for clinical treatment. At the same time, doctors and nurses will spend a lot of energy on dealing with false positives and wasting hospital resources. According to the American Heart Association, less than a quarter of hospitalized patients with cardiac arrest can survive.

In addition, the ECG signal is the embodiment of the myocardial electrical activity process. Therefore, in addition to the heart rate, the ECG signal can also display a large amount of information about the heart state. When there is a problem with the heart state, the ECG signal will change accordingly, and sometimes it is not necessarily reflected in the heart rate. The current multi-parameter monitoring device can only perform very limited analysis and alarm on the ECG signal, which also leads to a large number of missed events, and the patient's life and health cannot be effectively protected.

Summary of the invention

It is an object of the present invention to provide a multi-parameter monitoring data analysis method and a multi-parameter monitoring system that are proposed to solve the deficiencies of the prior art.

A first aspect of the embodiments of the present invention provides a multi-parameter monitoring data analysis method, including:

The monitoring device receives the monitoring reference data input by the user or sent by the workstation; the monitoring reference data includes the measured object information, and the physical data threshold and the electrocardiographic abnormal event information corresponding to the measured object information;

The monitor performs physical sign monitoring data collection on the measured object to obtain the vital sign monitoring data of the measured object; the vital sign monitoring data has time attribute information and monitor ID information, and the vital sign monitoring data includes: electrocardiogram data, Pulse data, blood pressure data, respiratory data, blood oxygen saturation data, and body temperature data;

The monitor performs wave group feature recognition on the electrocardiogram data, obtains a characteristic signal of the electrocardiogram data, performs heartbeat classification on the electrocardiogram data according to the feature signal, and obtains heartbeat classification information according to the basic rule reference data of the electrocardiogram And generating electrocardiogram event data; the ECG event data including the monitor ID information;

The monitor determines corresponding ECG event information according to the ECG event data, and determines whether the ECG event information is the ECG abnormal event information; when the ECG abnormal event information is, outputting the first alarm information The first alarm information includes the ECG abnormal event information, alarm time information, and the monitor ID information;

Determining, by the monitor, one or more of the pulse data, blood pressure data, respiratory data, blood oxygen saturation data, and body temperature data whether there is abnormal data exceeding a corresponding set threshold, and generating other according to the abnormal data The abnormal event information; when the set threshold is exceeded, outputting the second alarm information; the second alarm information includes the other abnormal event information, the alarm time information, and the monitor ID information;

The monitor sends the first alarm information and/or the second alarm information to a workstation, so that the workstation generates a corresponding alarm output signal according to the first alarm information and/or the second alarm information. .

Preferably, the method further includes:

The monitor aggregates the vital sign monitoring data according to the time attribute information of the vital sign monitoring data, generates time series data of the vital sign monitoring data, and stores the time series data.

Preferably, the method further includes:

When the preset ECG abnormal event information is obtained, the ECG data in the preset time period before and after the corresponding time of the ECG data is acquired according to the time attribute information, and the abnormal event record data is generated;

The monitor generates association information of the abnormal event record data and the first alarm information, and sends the information to the workstation.

Further preferably, the method further comprises:

Receiving, by the monitor or the workstation, a reference instruction for the first alarm information or the second alarm information, acquiring corresponding abnormal event record data, and outputting, and/or analyzing and processing the abnormal event record data, Generate and output exception event report data.

Preferably, performing the wave group feature recognition on the electrocardiogram data, obtaining a characteristic signal of the electrocardiogram data, performing heart beat classification on the electrocardiogram data according to the feature signal, and obtaining a heart beat classification according to the basic rule reference data of the electrocardiogram Information and generate ECG event data specifically include:

Converting the data format of the electrocardiogram data into a preset standard data format by performing re-sampling, and performing first filtering processing on the ECG data of the converted preset standard data format;

Performing a heartbeat detection process on the electrocardiogram data after the first filtering process, and identifying a plurality of heartbeat data included in the electrocardiogram data, each of the heartbeat data corresponding to one heart cycle, including a corresponding P wave, QRS Wave group, T wave amplitude and start and end time data;

Determining a confidence level of each heartbeat based on the heartbeat data;

Performing interference recognition on the heartbeat data according to the interference recognition two-class classification model, obtaining whether the heartbeat data has interference noise, and a probability value for determining the interference noise;

Determining the validity of the heartbeat data according to the detection confidence, and, according to the lead parameter and the heartbeat data determining the valid heartbeat data, combining the result of the interference recognition and the time rule to generate the heartbeat time series data; Generating heartbeat analysis data according to the heartbeat time series data;

Performing feature extraction and analysis of the amplitude and time characterization data on the heartbeat analysis data according to a heartbeat classification model to obtain primary classification information of the cardiac analysis data;

The heartbeat analysis data of the specific heartbeat in the primary classification information result is input to the ST segment and the T wave change model for identification, and the ST segment and T wave evaluation information is determined;

Performing P wave and T wave feature detection on the heartbeat analysis data according to the heartbeat time series data, and determining detailed feature information of P wave and T wave in each heart beat, the detailed feature information includes amplitude, direction, Form and start and end time data;

Performing secondary classification processing on the heartbeat analysis data according to the electrocardiogram basic rule reference data, the detailed feature information of the P wave and the T wave, and the ST segment and T wave evaluation information under the primary classification information, Get heartbeat classification information;

The heartbeat classification information is analyzed and matched to generate the ECG event data.

The multi-parameter monitoring data analysis method provided by the embodiment of the invention realizes the data analysis and alarm flow of the multi-parameter monitoring based on the artificial intelligence, and can automatically, quickly and completely analyze the measurement data obtained by the monitor, and the abnormality is The ECG status and other vital signs parameters are given an alert and uploaded to the workstation. The method can reduce the false alarm phenomenon caused by the interference, the alarm accuracy is high, and the types of abnormalities that can be detected, especially the types of abnormalities of the electrocardiogram, have a good application prospect.

A second aspect of the embodiments of the present invention provides a multi-parameter monitoring data analysis method, including:

The monitor performs physical condition monitoring data collection on the measured object, obtains the vital sign monitoring data of the measured object, and acquires the measured object information, and sends the physical condition monitoring data and the measured object information to the workstation; The vital sign monitoring data has time attribute information and monitor ID information, and the vital sign monitoring data includes: electrocardiogram data, pulse data, blood pressure data, respiratory data, blood oxygen saturation data, and body temperature data;

The workstation performs wave group feature recognition on the electrocardiogram data, obtains a characteristic signal of the electrocardiogram data, performs heartbeat classification on the electrocardiogram data according to the characteristic signal, and obtains heartbeat classification information according to the basic rule reference data of the electrocardiogram, And generating ECG event data; the ECG event data includes the monitor ID information;

The workstation determines monitoring reference data according to the measured object information; the monitoring reference data includes a vital sign data threshold and an electrocardiographic abnormal event information corresponding to the measured object information;

Determining, according to the electrocardiogram event data, the corresponding ECG event information, and determining whether the ECG event information is a preset ECG abnormal event information; and when the preset ECG abnormal event information is generated, generating a first alarm Information; the first alarm information includes the ECG abnormal event information, alarm time information, and the monitor ID information;

The workstation determines whether one or more of the pulse data, blood pressure data, respiratory data, blood oxygen saturation data, and body temperature data have abnormal data exceeding a corresponding set threshold, and generates other abnormalities according to the abnormal data. Event information; when the set threshold is exceeded, generating second alarm information; the second alarm information includes the other abnormal event information, alarm time information, and the monitor ID information;

The workstation outputs the first alarm information and/or the second alarm information, and sends the first alarm information and/or the second alarm information to the monitor according to the monitor ID information And causing the monitor to generate a corresponding alarm output signal according to the first alarm information and/or the second alarm information.

Preferably, the method further includes:

The workstation aggregates the vital sign monitoring data according to the time attribute information of the vital sign monitoring data, generates time series data of the vital sign monitoring data, and stores the time series data.

Preferably, the method further includes:

When it is the preset ECG abnormal event information, the workstation acquires the electrocardiogram data in the preset time period before and after the corresponding time of the ECG data according to the time attribute information, and generates abnormal event record data;

The workstation generates association information of the abnormal event record data and the first alarm information.

Preferably, the method further includes:

Receiving, by the workstation, a reference instruction for the first alarm information or the second alarm information, acquiring corresponding abnormal event record data and outputting, and/or analyzing and processing the abnormal event record data, generating and outputting an abnormal event Report data.

Further preferably, the method further comprises:

The monitor receives a review instruction for the first alarm information or the second alarm information;

Sending the lookup instruction to the workstation;

The workstation acquires the abnormal event record data, and/or analyzes and processes the abnormal event record data to generate abnormal event report data;

The abnormal event record data and/or abnormal event report data is transmitted to the monitor.

Preferably, performing the wave group feature recognition on the electrocardiogram data, obtaining a characteristic signal of the electrocardiogram data, performing heart beat classification on the electrocardiogram data according to the feature signal, and obtaining a heart beat classification according to the basic rule reference data of the electrocardiogram Information and generate ECG event data specifically include:

Converting the data format of the electrocardiogram data into a preset standard data format by performing re-sampling, and performing first filtering processing on the ECG data of the converted preset standard data format;

Performing a heartbeat detection process on the electrocardiogram data after the first filtering process, and identifying a plurality of heartbeat data included in the electrocardiogram data, each of the heartbeat data corresponding to one heart cycle, including a corresponding P wave, QRS Wave group, T wave amplitude and start and end time data;

Determining a confidence level of each heartbeat based on the heartbeat data;

Performing interference recognition on the heartbeat data according to the interference recognition two-class classification model, obtaining whether the heartbeat data has interference noise, and a probability value for determining the interference noise;

Determining the validity of the heartbeat data according to the detection confidence, and, according to the lead parameter and the heartbeat data determining the valid heartbeat data, combining the result of the interference recognition and the time rule to generate the heartbeat time series data; Generating heartbeat analysis data according to the heartbeat time series data;

Performing feature extraction and analysis of the amplitude and time characterization data on the heartbeat analysis data according to a heartbeat classification model to obtain primary classification information of the cardiac analysis data;

The heartbeat analysis data of the specific heartbeat in the primary classification information result is input to the ST segment and the T wave change model for identification, and the ST segment and T wave evaluation information is determined;

Performing P wave and T wave feature detection on the heartbeat analysis data according to the heartbeat time series data, and determining detailed feature information of P wave and T wave in each heart beat, the detailed feature information includes amplitude, direction, Form and start and end time data;

Performing secondary classification processing on the heartbeat analysis data according to the electrocardiogram basic rule reference data, the detailed feature information of the P wave and the T wave, and the ST segment and T wave evaluation information under the primary classification information, Get heartbeat classification information;

The heartbeat classification information is analyzed and matched to generate the ECG event data.

The multi-parameter monitoring data analysis method provided by the embodiment of the invention realizes the data analysis and alarm flow of the multi-parameter monitoring based on artificial intelligence, and can automatically, quickly and completely analyze the measurement data uploading workstation monitored by the monitor, The abnormal ECG status and other vital signs parameters give an early warning, and the alarm information is sent to the monitor. This method can reduce the false alarm phenomenon caused by the interference, the alarm accuracy is high, and the detectable abnormal type, especially the abnormal electrocardiogram There are many types and good application prospects.

A third aspect of the embodiments of the present invention provides a multi-parameter monitoring system, comprising the monitor and workstation according to the above first aspect;

The monitor includes: a memory for storing a program, and a processor for performing the method of the first aspect described above.

A fourth aspect of the embodiments of the present invention provides a computer program product comprising instructions for causing a computer to execute the methods of the first aspect and the implementations of the first aspect when the computer program product is run on a computer.

A fifth aspect of the embodiments of the present invention provides a computer readable storage medium. The computer readable storage medium stores a computer program. When the computer program is executed by the processor, the first aspect and the method in each implementation manner of the first aspect are implemented. .

A sixth aspect of the embodiments of the present invention provides a multi-parameter monitoring system, comprising: the monitor and the workstation according to the second aspect;

The workstation includes a memory and a processor; the memory is for storing a program, and the processor is configured to perform the method of the second aspect described above.

A seventh aspect of the embodiments of the present invention provides a computer program product comprising instructions for causing a computer to perform the methods of the second aspect and the implementations of the second aspect when the computer program product is run on a computer.

An eighth aspect of the embodiments of the present invention provides a computer readable storage medium. The computer readable storage medium stores a computer program. When the computer program is executed by the processor, the method in the implementation manners of the second aspect and the second aspect is implemented. .

DRAWINGS

1 is a flowchart of a multi-parameter monitoring data analysis method according to an embodiment of the present invention;

2 is a flowchart of a method for processing electrocardiogram data according to an embodiment of the present invention;

FIG. 3 is a schematic diagram of a two-classification model for interference recognition according to an embodiment of the present invention; FIG.

4 is a schematic diagram of a heart beat classification model according to an embodiment of the present invention;

FIG. 5 is a schematic diagram of a ST segment and T wave change model according to an embodiment of the present invention; FIG.

FIG. 6 is a schematic structural diagram of a multi-parameter monitor according to an embodiment of the present invention;

FIG. 7 is a flowchart of another multi-parameter monitoring data analysis method according to an embodiment of the present invention;

FIG. 8 is a schematic structural diagram of another multi-parameter monitor according to an embodiment of the present invention.

Detailed ways

The technical solution of the present invention will be further described in detail below through the accompanying drawings and embodiments.

The present invention relates to a multi-parameter monitoring data analysis method for clinical monitoring, and a multi-parameter monitoring system for performing the method. The multi-parameter monitoring system includes one or more multi-parameter monitors and a workstation connected to the multi-parameter monitor. The multi-parameter monitor and the workstation can be connected by wire or wirelessly, and the wireless connection includes but is not limited to the wireless local area network (WIFI) based on the IEEE 802.11b standard, Bluetooth, 3G/4G/5G mobile communication network, Internet of Things, etc. .

The multi-parameter monitor is a clinical medical monitoring device. This kind of monitoring device is characterized by multiple sets of sensors, which can simultaneously monitor vital signs such as ECG, blood pressure, blood oxygen, pulse, respiration, body temperature, etc., and process the data transmitted from each sensor in real time, and the abnormality occurs in the corresponding indicators. When the alarm signal is given, the doctor and nurse can handle the condition in time.

Among the vital signs such as ECG, blood pressure, blood oxygen, pulse, respiration, and body temperature detected by the multi-parameter monitor, the monitoring of ECG is different from other parameters. The ECG signal obtained through the sensor needs to pass a series of complexities. The algorithm calculation can extract the effective information among them. Compared with other signals, the processing process is more complicated and difficult, and it is also a link that is prone to detection errors.

The ECG signal is the weak current reflected by the electrical activity of the cardiomyocytes on the body surface, recorded by the body surface electrode and the amplified recording system. Other non-cardiogenic electrical signals, such as EMG signal interference caused by skeletal muscle activity, are also recorded during the recording process. Therefore, we believe that it is necessary to effectively identify and eliminate the interference of the heart signal to effectively reduce the false alarm caused by the interference signal.

In addition, the ECG signal is the embodiment of the myocardial electrical activity process. Therefore, in addition to the heart rate, the ECG signal can also display a large amount of information about the heart state. When there is a problem with the heart state, the ECG signal will change accordingly. In the process of researching the existing multi-parameter monitoring equipment in the industry, we found that the existing monitoring equipment can only perform very limited analysis and alarm on the ECG signal. In addition to this, in addition to effective interference identification and elimination of ECG signals to reduce false positives caused by interference signals, we believe that it can be improved from the following points:

First, the use of reasonable filtering parameter settings and threshold settings during heartbeat monitoring can avoid multiple detections and missed detections of heartbeat detection, such as for some special ECG signals, such as tall T waves of patients with slow heart rhythms, or T waves. Multiple tests of hypertrophic signals.

Second, the classification of heart beats is more detailed, and not only in the three categories of sinus, supraventricular and ventricular, so as to meet the complex and comprehensive analysis requirements of clinical electrocardiographers.

Third, accurate identification of atrial flutter and ST-T changes can help provide analysis of ST-segment and T-wave changes for myocardial ischemia.

Fourth, accurate identification of heartbeat and ECG events.

In the present invention, in view of the above points, through the analysis and calculation of the electrocardiographic data, especially the introduction of artificial intelligence (AI) technology, the arrhythmia analysis, long interval pause, flutter and flutter are performed on the collected digital signals, Conduction block, premature beat and escape, bradycardia, tachycardia, ST segment change detection, ECG event analysis and classification, in order to achieve the purpose of generating accurate alarm signals, so as to effectively monitor the patient's vital signs.

To this end, the present invention provides a multi-parameter monitoring data analysis method in the first embodiment. The method step flow is shown in FIG. 1 , and the method mainly includes the following steps:

Step 100: The monitor receives monitoring reference data input by the user or sent by the workstation;

Specifically, the monitoring reference data includes the measured object information, and the physical data threshold and the electrocardiographic abnormal event information corresponding to the measured object information;

For pulse data, blood pressure data, respiratory data, blood oxygen saturation data, and body temperature data, corresponding parameter thresholds corresponding to different types of measured objects can be specifically set. When the monitoring baseline data is selected, it can be selected according to the actual situation of the monitored person.

For example, the setting of the threshold value of the pulse data and respiratory data of the newborn is higher than that of the ordinary adult. In practical applications, the appropriate parameter threshold can be selected according to the needs, so that the multi-parameter monitor can be very good. Match the monitored person to achieve effective monitoring and accurate alarm.

The ECG abnormal event information refers to an abnormal ECG event that needs to generate an alarm.

The monitoring reference data can be input on the monitor, and the existing parameter threshold can be selected from the local storage unit of the monitor, or the data can be directly input, or can be obtained by the workstation through a network or a connection line, that is, the workstation can be Active distribution, or it can be a data request from the monitor.

Step 110: The monitor performs physical sign monitoring data collection on the measured object, and obtains vital sign monitoring data of the measured object;

Specifically, the object to be measured refers to a living body that is monitored by a multi-parameter monitor, wherein the most conventional object to be measured refers to a person.

The monitor has a vital sign signal collecting device such as an electrode, a probe, a cuff, and the like, which is in contact with the object to be measured, and collects a vital sign signal of the measured object through the sign signal collecting device, and obtains the vital sign monitoring data through digital processing. The vital signs monitoring data may specifically include: electrocardiogram data, pulse data, blood pressure data, respiratory data, blood oxygen saturation data, and body temperature data. The vitality monitoring data has time attribute information, and each data point has a corresponding data collection time, which is time attribute information. At the same time as data acquisition, this data acquisition time is also recorded and stored as time attribute information of the vitals monitoring data. The vital sign monitoring data also has monitor ID information. When the physical monitoring data is collected, the information of the monitor for collecting the data, that is, the monitor ID information, is simultaneously recorded in the collected vital sign monitoring data.

In order to better understand the intent and implementation of the present invention, the following describes the methods and principles for collecting various types of physical monitoring data:

ECG data: The signals generated by the electrocardiographic signal collection of the ECG signal acquisition team by the non-invasive ECG are recorded in single-lead or multi-lead form.

Pulse data: The pulse is a phenomenon in which the arteries periodically pulsate as the heart contracts. The pulse includes changes in various physical quantities such as intravascular pressure, volume, displacement, and wall tension. We prefer to use photoelectric volumetric pulse measurement. The sensor consists of two parts, a light source and a photoelectric transducer, which can be clamped on the fingertip or auricle of the subject. The light source selects a wavelength that is selective for oxyhemoglobin in the arterial blood, such as a light-emitting diode having a spectrum of 700-900 nm. The light passes through the perivascular blood vessels of the human body. When the volume of arterial congestion changes, the light transmittance of the light is changed. The photoelectric transducer transmits the light transmitted or reflected by the tissue, and is converted into an electrical signal to be amplified and output by the amplifier. This reflects the volume change of the arterial blood vessels. The pulse is a signal that periodically changes with the pulsation of the heart, and the volume of the arterial vessel also changes periodically. The period of signal change of the photoelectric transducer is the pulse rate, that is, the pulse data.

Blood pressure data: The highest pressure reached during systole is called systolic blood pressure, which pushes blood into the aorta and maintains systemic circulation. The lowest pressure reached when the heart expands is called diastolic blood pressure, which allows blood to flow back into the right atrium. The integral of the blood pressure waveform over one week divided by the cardiac period T is called the average pressure. There are many ways to measure blood pressure data, which can be divided into invasive measurements and non-invasive measurements. In the multi-parameter monitor, we prefer two types of non-invasive measurement methods, the Korotkoff method and the vibration measurement method. The Korotkoff method is to detect the Korotkoff sound (pulse sound) under the cuff to measure blood pressure. The Korotkoff sound non-invasive blood pressure monitoring system includes a cuff inflation system, a cuff, a Korotkoff sound sensor, an audio amplification and an automatic gain adjustment circuit. , A / D converter, microprocessor and display parts. The vibration measurement method is to detect the oscillating wave of the gas in the sleeve, the oscillation wave originates from the pulsation of the blood vessel wall, and the blood pressure data can be measured by measuring the relevant points of the oscillation wave, including systolic blood pressure (PS), diastolic blood pressure (PD) and average pressure (PM). ). The method of obtaining the pulse vibration wave by the vibration measuring method can obtain the blood pressure data by measuring the pulse vibration wave by means of the microphone and the pressure sensor. For some special application scenarios, blood pressure data can also be obtained by invasive measurement. For example, some patients in the intensive care unit (ICU) ward can be monitored by directly intubating the artery and connecting the other end of the cannula to a sterilized fluid-filled pressure detection system to achieve real-time blood pressure data. collection. The advantages of this invasive monitoring method include: the display of blood pressure in real time, and the display of continuous blood pressure changes; accurate readings in hypotensive states; long-term patient comfort is improved, avoiding non-invasive measurements The wound caused by long-term inflation and deflation; more information can be extracted, including the vascular volume can be derived from the shape of the blood pressure waveform.

Respiratory data: Respiratory measurements are an important part of the kinetic energy test. The monitor measures the respiratory rate (times/minute) by measuring the respiratory wave, which is the respiratory data. The measurement of the respiratory rate can directly measure the temperature change of the respiratory airflow through the thermistor, and the change is converted into a voltage signal through the bridge circuit; the impedance method can also be used to measure the respiratory frequency, because the chest wall muscles are alternating when breathing The thoracic shape is alternately deformed, and the electrical impedance of the body tissue also alternates. The measurement of the respiratory impedance value can be performed by various methods such as a bridge method, a modulation method, a constant voltage source method, and a constant current source method. In the monitor, the respiratory impedance electrode can also be used in combination with the ECG electrode, and the respiratory impedance change and the respiratory rate can be detected simultaneously when the ECG signal is detected.

Blood oxygen saturation data: Blood oxygen saturation is an important parameter to measure the ability of human blood to carry oxygen. The oxygen saturation can be measured by transmission (or reflection) dual-wavelength (red R and infrared IR) photodetection techniques to detect the ratio of alternating components caused by the absorption of red and infrared light through arterial blood. The non-pulsating tissue (skin, muscle, venous blood, etc.) causes a stable component (direct current) value of light absorption, and the blood oxygen saturation value SpO2, that is, blood oxygen saturation data, can be obtained by calculation. Since the pulsation law of the photoelectric signal is consistent with the law of the heart beat, the pulse data can be simultaneously determined according to the period of the detected signal.

Body temperature data: Body temperature is an important indicator of life status. The body temperature is measured using a thermistor with a negative temperature coefficient as the temperature sensor, and a bridge is used as the detection circuit. In specific applications, we can use integrated temperature measurement circuit to measure body temperature data. It is also possible to use two or more temperature measuring circuits to measure the temperature difference between two different parts to correct the measured value. Body surface probes and body cavity probes can also be used to monitor body surface and cavity temperature, respectively. In some special applications, in order to avoid cross-contagion, infrared non-contact temperature measurement technology can also be used to monitor body temperature data. In the monitor, we set the temperature measurement accuracy to 0.1 °C in order to have a faster temperature response.

In the present invention, we can use the multi-parameter monitor to perform the physical monitoring data collection of the measured object by the above method, and obtain the vital sign monitoring data of the measured object.

After the physical monitoring data is obtained, the corresponding data identification and abnormality judgment can be performed according to the physical monitoring data, and corresponding alarms are generated for different abnormalities, thereby effectively monitoring the function.

As mentioned above, the monitoring of ECG is more complicated than the monitoring of other vital signs such as blood pressure, blood oxygen, pulse, respiration, body temperature, etc. Therefore, in the present invention, the electrocardiogram data is different from other physical monitoring data. The processing method specifically adopts the automatic analysis method of electrocardiogram based on artificial intelligence self-learning to identify, process and abnormally judge the electrocardiogram data.

The following steps 120-140 are processes for ECG data, and steps 150 and 160 are processes for other vitals monitoring data such as pulse data, blood pressure data, respiratory data, blood oxygen saturation data, and body temperature data. The two processes can be executed synchronously without the limitation of sequential execution.

Step 120: The monitor performs wave group feature recognition on the electrocardiogram data, obtains a characteristic signal of the electrocardiogram data, performs heart beat classification on the electrocardiogram data according to the characteristic signal, obtains heart beat classification information according to the basic rule reference data of the electrocardiogram, and generates ECG event data;

Specifically, the ECG data processing process of the present invention adopts an artificial intelligence self-learning automatic ECG analysis method, which is implemented based on an artificial intelligence convolutional neural network (CNN) model. The CNN model is a supervised learning method in deep learning. It is a multi-layer network (hidden layer) connection structure that simulates a neural network. The input signal passes through each hidden layer in turn, and a series of complicated mathematical processing (Convolution volume) is performed. Product, Pooling Pooling, Regularization Regularization, Prevention of Overfitting, Dropout Temporary Discarding, Activation Activation, Relu Activation Function), automatically abstracting some features of the object to be identified layer by layer, and then passing these features as input The higher layer of the hidden layer is calculated until the last layer of the Full Connection reconstructs the entire signal, using the Softmax function for logistic regression to achieve multi-target classification.

CNN belongs to the supervised learning method in artificial intelligence. During the training phase, the input signal passes through multiple hidden layer processing to reach the final fully connected layer. The classification result obtained by softmax logistic regression is related to the known classification result (label label). There will be an error. A core idea of deep learning is to continually minimize this error through a large number of sample iterations, and then calculate the parameters that connect the hidden layer neurons. This process generally requires constructing a special cost function, using a nonlinearly optimized gradient descent algorithm and a backpropagation algorithm (BP) to quickly and efficiently minimize the entire depth (the number of layers in the hidden layer). ) and breadth (dimension dimension) are all complex parameters in the neural network structure.

Deep learning inputs the data to be identified into the training model, passes through the first hidden layer, the second hidden layer, the third hidden layer, and finally outputs the recognition result.

In the present invention, the wave group feature recognition, the interference recognition, the heart beat classification and the like of the electrocardiogram data are all based on the artificial intelligence self-learning training model to obtain an output result, and the analysis speed is fast and the accuracy is high.

Specifically, the electrocardiogram data processing process of the present invention is performed in a monitor, comprising performing wave group feature recognition on the electrocardiogram data, obtaining a characteristic signal of the electrocardiogram data, performing cardiac beat classification on the electrocardiogram data according to the characteristic signal, and combining the basic rules of the electrocardiogram The reference data is obtained by the heartbeat classification information, and the generation of the electrocardiogram event data can be specifically realized by the following steps as shown in FIG. 2. This process is real-time, so the processing results can be obtained quickly and in real time.

Step 121: The data format of the electrocardiogram data is resampled into a preset standard data format, and the first filtering process is performed on the ECG data of the converted preset standard data format.

Specifically, the format of the ECG data is read and read, and different reading operations are implemented for different devices. After reading, the baseline needs to be adjusted and converted into millivolt data according to the gain. After data resampling, the data is converted to a sampling frequency that can be processed by the entire process. Then, high frequency, low frequency noise interference and baseline drift are removed by filtering to improve the accuracy of artificial intelligence analysis. The processed ECG data is saved in a preset standard data format.

Through this step, the difference between the use of different leads, the sampling frequency and the transmission data format, and the removal of high frequency, low frequency noise interference and baseline drift by digital signal filtering are solved.

Digital signal filtering can use high-pass filter, low-pass filter and median filter to eliminate power frequency interference, myoelectric interference and baseline drift interference, and avoid the impact on subsequent analysis.

More specifically, a low-pass, high-pass Butterworth filter can be used for zero-phase shift filtering to remove baseline drift and high-frequency interference, retaining an effective ECG signal; median filtering can be performed using a preset duration of sliding window The median of the data point voltage magnitude replaces the amplitude of the center sequence of the window. The low frequency baseline drift can be removed.

Step 122: Perform heartbeat detection processing on the electrocardiogram data after the first filtering process, and identify multiple heartbeat data included in the electrocardiogram data;

Each heart beat data corresponds to a heart cycle, including the corresponding P wave, QRS complex, T wave amplitude and start and end time data. The heartbeat detection in this step is composed of two processes, one is a signal processing process, and the characteristic frequency band of the QRS complex is extracted from the electrocardiogram data after the first filtering; the second is to determine the QRS complex by setting a reasonable threshold The time of occurrence. In an electrocardiogram, a P wave, a QRS complex, a T wave component, and a noise component are generally included. In general, the QRS complex has a frequency range of 5 to 20 Hz, and the QRS complex signal can be proposed by a bandpass filter within this range. However, the frequency bands of the P wave and the T wave and the frequency band of the noise and the QRS complex frequency band partially overlap, so the signal processing method cannot completely remove the signal of the non-QRS wave group. It is therefore necessary to extract the QRS complex position from the signal envelope by setting a reasonable threshold. The specific detection process is a process based on peak detection. Threshold judgment is performed for each peak sequence in the signal. When the threshold value is exceeded, the QRS group judgment process is entered, and more features are detected, such as RR interval and shape.

Multi-parameter monitors are often recorded for long periods of time, and the amplitude and frequency of the beat signal in the process center are constantly changing, and in the disease state, this characteristic will be more powerful. When the threshold is set, the threshold adjustment needs to be dynamically performed according to the change of the data characteristics in the time domain. In order to improve the accuracy and positive rate of detection, QRS complex detection mostly adopts the dual amplitude threshold combined with the time threshold. The high threshold has a higher positive rate, the lower threshold has a higher sensitivity rate, and the RR interval exceeds a certain period. The time threshold is detected using a low threshold to reduce missed detection. Since the low threshold is low due to the low threshold, it is susceptible to T wave and myoelectric noise, and it is easy to cause multiple tests. Therefore, high threshold is preferred for detection.

There are lead parameters for heartbeat data for different leads to characterize which heartbeat data the heartbeat data is. Therefore, when the ECG data is obtained, the information of the lead can be determined according to the transmission source, and this information is used as the lead parameter of the heartbeat data.

Step 123: Determine a detection confidence level of each heart beat according to the heart beat data;

Specifically, in the process of heartbeat detection, the confidence calculation module can provide an estimate of the confidence of the QRS complex detection based on the amplitude of the QRS complex and the amplitude ratio of the noise signal during the RR interval.

Step 124: Perform interference recognition on the heartbeat data according to the interference recognition two-class model, obtain whether the heartbeat data has interference noise, and a probability value for determining the interference noise;

Because the multi-parameter monitor is susceptible to interference due to various influences during the long-term recording process, the acquired heartbeat data is invalid or inaccurate, and cannot correctly reflect the condition of the subject, and also increases the difficulty and workload of the doctor; And interference data is also a major factor that causes intelligent analysis tools to work effectively. Therefore, it is especially important to minimize external signal interference.

This step is based on the end-to-end two-category recognition model with deep learning algorithm as the core. It has the characteristics of high precision and strong generalization performance, which can effectively solve the disturbance problem caused by the main interference sources such as electrode stripping, motion interference and static interference. It overcomes the problem that the traditional algorithm has poor recognition effect due to the diversity and irregularity of the interference data.

This can be achieved by the following methods:

Step A, using interference recognition two-class model for heart rate data for interference recognition;

Step B, identifying a data segment in the heartbeat data that the heartbeat interval is greater than or equal to the preset interval determination threshold;

Step C: performing signal abnormality determination on the data segment whose heartbeat interval is greater than or equal to the preset interval determination threshold, and determining whether it is an abnormal signal;

Among them, the identification of the abnormal signal mainly includes whether the electrode piece is off, low voltage, and the like.

Step D, if it is not an abnormal signal, determine a starting data point and a ending data point of the sliding sample in the data segment according to the set time value by a preset time width, and start sliding sampling the data segment from the starting data point, Obtaining a plurality of sampled data segments until the data point is terminated;

In step E, interference identification is performed for each sampled data segment.

The above steps A-E will be described with a specific example. The heartbeat data of each lead is cut and sampled by the set first data amount, and then input to the interference recognition two-classification model for classification, and a probability value of the interference recognition result and the corresponding result is obtained; for the heartbeat interval If the heartbeat data is greater than or equal to 2 seconds, first determine whether the signal is overflowing, low voltage, and the electrode is off; if not, according to the first data amount, starting from the left heartbeat, continuing to the right continuously without overlapping the first data amount Sliding sampling for identification.

The input may be the first data volume heartbeat data of any lead, and then the interference identification two-class model is used for classification, and the direct output is the interference classification result, and the obtained result is fast, the accuracy is high, the stability is good, and the subsequent Analysis provides more effective and quality data.

Because the interference data is often caused by the external disturbance factor, there are mainly the electrode piece falling off, low voltage, static interference and motion interference. The interference data generated by different disturbance sources is different, and the interference data generated by the same disturbance source is different. At the same time, considering the interference data, although the diversity is wide, but it is very different from the normal data, it is also possible to ensure the diversity when collecting the interference training data, and take the sliding sampling of the moving window. It is possible to increase the diversity of the interference data so that the model is more robust to the interference data. Even if the future interference data is different from any previous interference, the similarity with the interference is greater than the normal data. The ability of the model to identify interfering data is enhanced.

The interference identification two-class model used in this step can be as shown in Figure 3. The network first uses two layers of convolutional layers. The convolution kernel size is 1x5, and each layer is followed by a maximum pool. The number of convolution kernels starts at 128, and the number of convolution kernels doubles each time the largest pooling layer is passed. The convolutional layer is followed by two fully connected layers and a softmax classifier. Since the classification number of the model is 2, softmax has two output units, which in turn correspond to the corresponding categories, and uses cross entropy as the loss function.

For the training of this model, we used nearly 4 million accurate data segments from 300,000 patients. Labels fall into two categories: normal ECG signals or segments of ECG signals with significant interference. We use segmented annotations with custom-developed tools and then save the interference segment information in a custom standard data format.

During the training process, two GPU servers were used for dozens of round-robin training. In a specific example, the sampling rate is 200 Hz, the data length is a segment D[300] of 300 ECG voltage values (millivolts), and the input data is: InputData(i,j), where i is the ith Lead, j is the jth segment D of the lead i. All the input data is randomly dispersed to start training, which ensures the convergence of the training process. At the same time, it controls the collection of too many samples from the same patient's ECG data, improving the generalization ability of the model, and the accuracy of the real scene. After the training converges, using 1 million independent test data for testing, the accuracy rate can reach 99.3%. Another specific test data is shown in Table 1 below.

	interference	normal
Sensitivity	99.14%	99.32%
Positive Predicitivity	96.44%	99.84%

Table 1

Step 125, determining validity of the heartbeat data according to the detection confidence, and, according to the lead parameter and the heartbeat data determining the valid heartbeat data, combining the result of the interference recognition and the time rule to generate the heartbeat time series data, and Generating heartbeat analysis data based on cardiac time series data;

Specifically, due to the complexity of the ECG signal and the fact that each lead may be affected by different degrees of interference, there may be multiple detections and missed detections depending on the single lead, and the time characterization of the heartbeat results detected by different leads. The data is not aligned, so the heartbeat data of all leads needs to be combined according to the interference recognition result and the time rule to generate a complete heartbeat time series data, and the time characterization data of all the lead heartbeat data is unified. Wherein, the time characterization data is used to represent time information of each data point on the time axis of the electrocardiogram data signal. According to the unified heartbeat time series data, in the subsequent analysis and calculation, each lead heart rate data can be cut using a preset threshold to generate heartbeat analysis data of each lead required for specific analysis. .

The heartbeat data of each of the above leads needs to determine the validity of the heartbeat data according to the detection confidence obtained in step 123 before merging.

Specifically, the heartbeat data merging process performed by the lead heartbeat merging module is as follows: according to the refractory period of the reference data of the basic rule of the electrocardiogram, the time characterization data combination of the different lead heartbeat data is obtained, and the heartbeat data with large deviation is discarded. The above-mentioned time characterization data combination voting generates a merged heart beat position, the merged heart beat position is added to the combined cardiac beat time sequence, and the next set of heart beat data to be processed is moved, and the loop execution is performed until all the heart beat data are merged.

Among them, the ECG activity refractory period may preferably be between 200 milliseconds and 280 milliseconds. The acquired time characterization data combination of the different lead heartbeat data should satisfy the following condition: the time characterization data of the heartbeat data combination contains at least one time characterization data of the heartbeat data. When voting on the time-characteristic data combination of the heartbeat data, the number of leads using the detected heartbeat data is determined as a percentage of the effective number of leads; if the time of the heartbeat data is indicative of the position of the corresponding lead is a low voltage The lead, the interfering segment, and the electrode are considered to be inactive leads for this heartbeat data when the electrode is detached. When calculating the specific position of the combined heart beat, the time average of the heart beat data can be used to obtain the average value of the data. During the merge process, this method sets a refractory period to avoid false merges.

In this step, a unified heartbeat time series data is output through the merging operation. This step can simultaneously reduce the multi-detection rate and missed detection rate of the heart beat, and effectively improve the sensitivity and positive predictive rate of heart beat detection.

Step 126: Perform feature extraction and analysis on the amplitude and time characterization data of the heartbeat analysis data according to the heartbeat classification model, and obtain primary classification information of the heartbeat analysis data;

Specifically, different dynamic electrocardiograph devices have differences in signal measurement, acquisition, or output lead data. Therefore, a simple single-lead classification method or a multi-lead classification method can be used according to specific conditions. The multi-lead classification method includes two methods: lead voting decision classification method and lead synchronization association classification method. The lead voting decision classification method is based on the heartbeat analysis data of each lead to conduct independent lead classification, and then the result vote is merged to determine the voting result decision method of the classification result; the lead synchronous association classification method uses the heart beat for each lead Analyze data for simultaneous association analysis. The single-lead classification method is to analyze the heartbeat analysis data of the single-lead device, and directly use the corresponding lead model for classification, and there is no voting decision process. The following describes several classification methods described above.

Single-lead classification methods include:

According to the heartbeat time series data, the single-lead heartbeat data is cut to generate single-lead heartbeat analysis data, and the characteristics of the amplitude and time characterization data of the heartbeat classification model corresponding to the training are input. Extract and analyze to obtain a single-lead classification information.

The lead voting decision classification method may specifically include:

The first step is to cut the heartbeat data of each lead according to the heartbeat time series data, thereby generating heartbeat analysis data of each lead;

In the second step, according to the heartbeat classification model corresponding to each lead of the training, the feature extraction and analysis of the amplitude and time characterization data of each lead heartbeat analysis data are performed, and the classification information of each lead is obtained;

In the third step, the classification voting decision calculation is performed according to the classification information of each lead and the reference weight value reference coefficient, and the primary classification information is obtained. Specifically, the lead weight value reference coefficient is based on the Bayesian statistical analysis of the electrocardiogram data to obtain the voting weight coefficient of each lead for different heart beat classifications.

The lead synchronization association classification method may specifically include:

According to the heartbeat time series data, each lead heartbeat data is cut to generate heartbeat analysis data of each lead; and then the heartbeat analysis data of each lead is performed according to the trained multi-lead synchronous correlation classification model. Synchronous amplitude and time characterizing the feature extraction and analysis of the data, and obtaining a classification information of the heartbeat analysis data.

The synchronous correlation classification method input of the heart beat data is all the lead data of the dynamic electrocardiogram device. According to the heartbeat position of the heart beat analysis data, the data points of the same position and a certain length on each lead are intercepted and synchronously transmitted to the trained The artificial intelligence deep learning model performs computational analysis, and the output is that each heartbeat position point comprehensively considers all the lead ECG signal characteristics, and the accurate heart beat classification of the heartbeat associated with the heart rhythm characteristics in time.

The method fully considers that the different lead data of the electrocardiogram actually measures the information flow transmitted by the cardiac electrical signal in different vector directions of the electrocardiogram, and comprehensively analyzes the multi-dimensional digital features transmitted by the electrocardiogram signal in time and space. Greatly improved the traditional method only relying on a single lead independent analysis, and then the results are summarized into some statistical voting methods and the easy to get the classification error defects, greatly improving the accuracy of heart rate classification.

The heartbeat classification model used in this step can be as shown in Fig. 4. Specifically, it can be an end-to-end multi-label classification model inspired by the model of convolutional neural network AlexNet, VGG16, Inception based on artificial intelligence deep learning. Specifically, the model's network is a 7-layer convolutional network, with each convolution followed by an activation function. The first layer is a convolutional layer of two different scales, followed by six convolutional layers. The convolution kernels of the seven-layer convolution are 96, 256, 256, 384, 384, 384, 256, respectively. Except for the first-level convolution kernel, which has two scales of 5 and 11, respectively, the other layer has a convolution kernel scale of 5. The third, fifth, sixth and seventh layers of the convolutional layer are followed by the pooling layer. Finally followed by two fully connected layers.

In the heartbeat classification model in this step, we used a training set containing 17 million data samples from 300,000 patients for training. These samples are generated by accurately labeling the data according to the requirements of dynamic electrocardiogram analysis and diagnosis. The annotations are mainly for common arrhythmia, conduction block and ST segment and T wave changes, which can meet the model training of different application scenarios. The marked information is saved in a preset standard data format. In the preprocessing of training data, in order to increase the generalization ability of the model, a small sliding is performed on the classification with less sample size to amplify the data. Specifically, it is based on each heart beat and according to a certain step. (For example, 10-50 data points) move 2 times, which can increase the data by 2 times, and improve the recognition accuracy of the classified samples with less data. After the actual results are verified, the generalization ability has also been improved.

In a practical training process, two GPU servers are used for dozens of round-robin training. After the training is converged, 5 million independent test data is used for testing, and the accuracy rate can reach 91.92%.

The length of the interception of the training data may be 1 second to 10 seconds. For example, the sampling rate is 200 Hz, with a sampling length of 2.5 s, and the obtained data length is a segment D [500] of 500 ECG voltage values (millivolts), and the input data is: InputData (i, j), where i is The i-th lead, j is the j-th segment D of the lead i. All the input data is randomly dispersed to start training, which ensures the convergence of the training process. At the same time, it controls the collection of too many samples from the same patient's ECG data, improving the generalization ability of the model, and the accuracy of the real scene. During training, the segment data D corresponding to all the leads is synchronously input, and the lead data of multiple spatial dimensions (different cardiac axis vectors) of each time position is synchronously learned according to the multi-channel analysis method of image analysis, thereby Get a more accurate classification result than the conventional algorithm.

Step 127, inputting, to the ST segment and the T wave change model, the heartbeat analysis data of the specific heartbeat in the primary classification information result, and determining the ST segment and the T wave evaluation information;

The ST segment and T wave evaluation information is specifically the lead position information in which the ST segment and the T wave corresponding to the heartbeat analysis data are changed. Because clinical diagnosis requires localization of changes to ST segments and T waves to specific leads.

Among them, the specific heartbeat data of the primary classification information refers to the heartbeat analysis data including the sinus beat (N) and other heartbeat types that may contain ST changes.

The ST segment and T wave change lead positioning module inputs the specific heart beat data of the primary classification information into each lead according to each lead into an artificial intelligence deep learning training model for identifying the ST segment and the T wave change, and performs calculation analysis and output. The results indicate whether the characteristics of the lead segment conform to the conclusions of the ST segment and the T wave change, so that the information of the ST segment and the T wave change occurring in the specific lead, that is, the ST segment and the T wave evaluation information can be determined. The specific method may be: inputting the data of each lead heartbeat analysis of the sinus heartbeat in the primary classification information, inputting the ST segment and the T wave change model, and identifying and analyzing the sinus beat analysis data one by one to determine whether the sinus beat analysis data is There are ST segment and T wave changing characteristics and specific lead position information that occurs, and ST segment and T wave evaluation information is determined.

The ST segment and T wave change model used in this step can be as shown in Fig. 5, and can be an end-to-end classification model inspired by models such as artificial neural network deep learning based convolutional neural networks AlexNet and VGG16. Specifically, the model is a 7-layer network with 7 convolutions, 5 pools, and 2 full connections. The convolution kernel used for convolution is 1x5, and the number of filters for each layer is different. The number of layer 1 convolution filters is 96; the second layer convolution is combined with the third layer convolution, the number of filters is 256; the fourth layer convolution is combined with the fifth layer convolution, and the number of filters is 384; the number of the sixth layer convolution filter is 384; the number of the seventh layer convolution filter is 256; the first, third, fifth, sixth, and seventh layers of the convolution layer are pooled. Then there are two full connections, and finally the results are divided into two categories using the Softmax classifier. In order to increase the nonlinearity of the model and extract the features of higher dimensionality of the data, two convolutional modes are used.

Because the heartbeat with ST segment and T wave changes is relatively low in all heart beats, in order to balance the diversity of training data and the balance of data types of each category, no ST segment and T wave changes and ST segments are selected. The ratio of the training data to the T wave change is about 2:1, which guarantees the good generalization ability of the model in the classification process and does not appear to have a tendency to have more training data. Because the shape of the heart beat is diverse, the forms of different individuals are not the same. Therefore, in order to better estimate the distribution of each classification, the characteristics can be effectively extracted. The training samples are collected from individuals of different ages, weights, genders, and areas of residence. In addition, because the ECG data of a single individual in the same time period is often highly similar, in order to avoid over-learning, when acquiring data of a single individual, a small number of samples of different time periods are randomly selected from all the data; The patient's heartbeat morphology has large differences between individuals and high intra-individual similarity. Therefore, when dividing training and test sets, different patients are divided into different data sets to avoid the same individual data appearing in the training set at the same time. With the test set, the resulting model test results are closest to the real application scenario, ensuring the reliability and universality of the model.

Step 128: Perform P wave and T wave feature detection on the heartbeat analysis data according to the heartbeat time series data, and determine detailed feature information of the P wave and the T wave in each heart beat;

Specifically, the detailed feature information includes amplitude, direction, shape, and start and stop time data; in the analysis of the heartbeat signal, the features of the P wave, the T wave, and the QRS wave are also important basis in the analysis of the electrocardiogram.

In the P-wave and T-wave feature detection modules, the P-wave, T-wave and QRS complexes are extracted by calculating the position of the segmentation point in the QRS complex and the position of the P- and T-wave segmentation points. . It can be realized by QRS group cut point detection, single lead PT detection algorithm and multi-lead PT detection algorithm.

QRS group segmentation point detection: According to the QRS group segment power maximum point and the start and end points provided by the QRS complex detection algorithm, the R point, R' point, S point and S' point of the QRS group in a single lead are searched. When there is multi-lead data, the median of each segmentation point is calculated as the last segmentation point position.

Single-lead P-wave and T-wave detection algorithms: P-wave and T-wave are relatively low in amplitude relative to QRS complex, and the signal is gentle, which is easy to be submerged in low-frequency noise, which is a difficult point in detection. According to the result of QRS complex detection, the method uses a low-pass filter to perform third filtering on the signal after eliminating the influence of the QRS complex on the low frequency band, so that the relative amplitude of the PT wave is increased. The T wave is then found between the two QRS complexes by peak detection. Because the T wave is a wave group generated by ventricular repolarization, there is a clear lock-time relationship between the T wave and the QRS complex. Based on the detected QRS complex, the midpoint between each QRS complex and the next QRS complex (such as the range between 400ms and 600ms after the first QRS complex) is used as the T-wave detection. At the end point, the largest peak is selected as the T wave in this interval. Then select the peak with the largest amplitude among the remaining peaks as the P wave. At the same time, the direction and morphological characteristics of the P wave and the T wave are determined based on the peak and position data of the P wave and the T wave. Preferably, the cutoff frequency of the low pass filtering is set between 10-30 Hz.

Multi-lead P-wave and T-wave detection algorithms: In the case of multi-lead, since the generation time of each wave in the heart beat is the same, the spatial distribution is different, and the temporal and spatial distribution of noise is different, the traceability algorithm can be used to perform P, Detection of T waves. The signal is first subjected to QRS complex elimination processing and the signal is third filtered using a low pass filter to remove interference. Each individual component in the original waveform is then calculated by an independent component analysis algorithm. Among the separated independent components, according to the distribution characteristics of the peaks and the position of the QRS complex, the corresponding components are selected as the P-wave and T-wave signals, and the direction and morphological characteristics of the P-wave and the T-wave are determined.

Step 129: Perform secondary classification processing on the heartbeat analysis data according to the basic rule of the electrocardiogram, the detailed feature information of the P wave and the T wave, and the ST segment and the T wave evaluation information under one primary classification information to obtain the heartbeat classification information; The heartbeat classification information is analyzed and matched to generate ECG event data.

Specifically, the basic rule of ECG reference data is generated by following the basic rules describing the electrophysiological activity of cardiomyocytes and the clinical diagnosis of electrocardiogram in authoritative ECG textbooks, such as the minimum time interval between two heart beats, and the minimum of P and R waves. Interval, etc., is used to subdivide the classification information after heartbeat classification; mainly based on the inter-heart rate RR interval and the medical saliency of different heartbeat signals on each lead; the heartbeat review module is based on the electrocardiogram The basic rule reference data combined with the classification and recognition of a plurality of continuous heartbeat analysis data, and the detailed feature information of the P wave and the T wave, the ventricular heart beat classification is divided into finer heart beat classification, including: ventricular premature beat (V) , ventricular escape (VE), accelerated ventricular premature beats (VT), subventricular subtypic breakdown into supraventricular premature beats (S), atrial escape (SE), borderline escape (JE ) and atrial accelerated premature beats (AT) and so on.

In addition, through the secondary classification process, it is also possible to correct the misclassification identification of the reference data that does not conform to the basic rule of the electrocardiogram occurring in one classification. The subdivided heart beats are classified according to the reference data of the basic rules of the electrocardiogram, and the classification and identification which does not conform to the basic rule of the electrocardiogram are found, and the classification is corrected according to the RR interval and the classification marks before and after.

Specifically, after secondary classification, a variety of heartbeat classifications can be output, such as: normal sinus beat (N), complete right bundle branch block (N_CRB), complete left bundle branch block (N_CLB), indoor resistance Hysteresis (N_VB), first degree atrioventricular block (N_B1), pre-excitation (N_PS), premature ventricular contraction (V), ventricular escape (VE), accelerated ventricular premature beat (VT), supraventricular premature beats ( S), atrial escape (SE), borderline escape (JE), accelerated atrial premature beats (AT), atrial flutter (AF), artifacts (A) and other classification results.

Through this step, the calculation of the basal heart rate parameter can also be completed. The heart rate parameters of the basic calculation include: RR interval, heart rate, QT time, QTc time and other parameters.

Subsequently, according to the second classification result of the heart beat, the pattern matching is performed according to the basic rule of the electrocardiogram, and the ECG event data can be obtained. The ECG event data also includes the monitor ID information to indicate which monitor the data is derived from, so that it can quickly correspond to the corresponding ward, bed, and patient in practical applications. ECG event data can correspond to these typical ECG events, including but not limited to:

Supraventricular premature beat

Supraventricular premature beats

Supraventricular premature beats

Supraventricular premature beats

Atrial escape

Atrial escape rhythm

Junctional escape

Junctional escape rhythm

Non-paroxysmal supraventricular tachycardia

Fastest supraventricular tachycardia

Longest supraventricular tachycardia

Supraventricular tachycardia

Short-chamber supraventricular tachycardia

Atrial flutter - atrial fibrillation

Ventricular premature beat

Ventricular premature beats

Ventricular premature beats

Ventricular premature beats

Ventricular escape

Ventricular escape rhythm

Accelerated ventricular autonomic rhythm

Fastest ventricular tachycardia

Longest ventricular tachycardia

Ventricular tachycardia

Short ventricular tachycardia

Second degree sinus block

Second degree sinus block

Once atrioventricular block

Second degree type I atrioventricular block

Second degree type II atrioventricular block

Second degree type II (2:1) atrioventricular block

Height atrioventricular block

Complete left bundle branch block

Complete right bundle branch block

Indoor block

Pre-excitation syndrome

ST segment and T wave change

Longest RR interval

Step 130: The monitor determines corresponding ECG event information according to the ECG event data, and determines whether the ECG event information is the ECG abnormal event information;

Specifically, the monitor can determine the ECG event information corresponding to the different ECG events according to the ECG event data, for example, the event information corresponding to the ECG event, or the event information further summarized based on the ECG event, for example, transmitting various kinds of events. Blocking events are classified as anomalous events under the information of conduction block events.

The preset ECG abnormal event information is stored in the multi-parameter monitor, and the preset ECG abnormal event information is the corresponding event information of the ECG event that needs to generate an alarm, that is, an abnormal electrocardiogram that needs to generate an alarm. Event information for the event. These information can be stored locally in the multi-parameter monitor or stored in the memory of the multi-parameter monitor or in the network's memory, which can be obtained by the multi-parameter monitor.

When the ECG event data determines that the corresponding ECG event information is the preset ECG abnormal event information, step 140 is performed.

If the ECG event data determines that the corresponding ECG event information is not the preset ECG abnormal event information, it indicates that there is no abnormal ECG condition that needs to generate an alarm, and the monitoring of Step 110 is continued.

Step 140, outputting first alarm information;

Specifically, when the ECG event data determines that the corresponding ECG event information is preset ECG abnormal event information, the first alarm information is generated and output.

The first alarm information refers to the alarm information of the abnormality of the electrocardiogram, including the information of the abnormality of the electrocardiogram and the information of the alarm time and the ID of the monitor. Therefore, the first alarm information is generated based on the ECG abnormal event information and the alarm time information. The alarm time information may further be information about the time when the electrocardiographic abnormal event occurs, that is, the time information obtained from the time attribute information, or may be the information that the ECG event information is determined to be the preset ECG abnormal event information after processing the electrocardiogram data. System time information.

In order to distinguish different parameters, the ECG abnormal event information has corresponding project information, that is, an ECG project, which can indicate that the abnormal event is an ECG event.

The types of alarms that can generate alarm information output according to the present invention include, but are not limited to:

1. Sinus heart rate event:

a) sinus tachycardia

b) sinus bradycardia

2, supraventricular tachycardia

a) atrial tachycardia

b) atrial flutter

c) atrial fibrillation

d) compartment reentry

3, ventricular tachycardia

a) simple ventricular tachycardia

b) polymorphic ventricular tachycardia

c) bidirectional ventricular tachycardia

d) torsade ventricular tachycardia

e) premature ventricular tachycardia

f) room flutter

g) ventricular fibrillation

4, ST-T segment changes

a) R-on-t ventricular premature beats

b) R-on-P ventricular premature beats

c) alternating large T waves

5, conduction block

a) high degree second block

b) third-degree conduction block

The above process realizes the data analysis processing of the electrocardiogram data to the abnormal alarm output.

The output of the first alarm information may be output locally on the display of the multi-parameter monitor, or may be locally printed and output by the multi-parameter monitor, and may also be transmitted to the receiving end through a wired or wireless network, such as a workstation or a server (specifically Such as mobile devices) to meet different usage needs.

Step 150: The monitor determines whether one or more of pulse data, blood pressure data, respiratory data, blood oxygen saturation data, and body temperature data have abnormal data exceeding a corresponding set threshold;

In the process of actual data processing, step 150 and steps 120-140 may be performed in parallel or in any order, and there is no strict sequence between the two.

Specifically, for the pulse data, the blood pressure data, the respiratory data, the blood oxygen saturation data, and the body temperature data, the corresponding parameter threshold is determined by selecting the monitoring reference data.

When one or more of the above-mentioned vitality monitoring data exceeds the set parameter threshold, step 160 is performed; otherwise, step 110 is continued to continue the physical sign detection.

Step 160: The monitor generates other abnormal event information according to the abnormal data, and outputs the second alarm information;

Specifically, when the pulse data, the blood pressure data, the respiratory data, the blood oxygen saturation data, and the body temperature data have data exceeding a range of the corresponding set parameter, other abnormal event information is generated according to the specific excess item. The other abnormal event information has corresponding item information, which is used to indicate which item has abnormal data. Such as pulse, blood pressure, breathing, blood oxygen or body temperature.

The second alarm information refers to the alarm information of the above other abnormal events except the abnormality of the electrocardiogram, including other abnormal event information and alarm time information. Therefore, the second alarm information is generated based on other abnormal event information and alarm time information. The alarm time information may further be information about the time when other abnormal events occur, that is, the time information obtained from the time attribute information, or may be determined by processing other vital signs data other than the electrocardiogram data to determine other abnormalities in the monitoring data. Information about the system time of the event.

Similarly, the output of the second alarm information can be output locally on the display of the multi-parameter monitor, or printed locally by the multi-parameter monitor, and can also be transmitted to the receiving end through a network, such as a workstation or a server (specifically, such as moving Equipment) to meet different usage needs.

Step 170: The monitor sends the first alarm information and/or the second alarm information to the workstation, so that the workstation generates a corresponding alarm output signal according to the first alarm information and/or the second alarm information.

It has been mentioned in the above steps that after generating the first alarm information or the second alarm information, the monitor transmits the corresponding alarm information to the workstation in addition to the local alarm information. Therefore, the synchronous alarm output of the workstation and the monitor can be realized, so that other user equipments connected to the workstation or the workstation, such as an alarm information receiving terminal carried by the doctor, can synchronously receive the alarm information, thereby automatically realizing the synchronous distribution of the alarm information. Thereby achieving a fast response.

In addition, the multi-parameter monitoring data analysis method of the present invention can also record data before and after the occurrence of an abnormal event, so that the abnormality analysis can be conveniently performed.

To this end, the multi-parameter monitor of the present invention can summarize the vital sign monitoring data based on the time attribute information of the vital sign monitoring data, generate time series data of the vital sign monitoring data, and store it.

When it is determined that an abnormal event corresponding to the preset ECG abnormal event information occurs, the ECG data in the preset time period before and after the abnormal event occurrence time is acquired according to the time attribute information corresponding to the abnormal event information, and the abnormal event record data is generated. At the same time, the association information of the abnormal event record data and the first alarm information is generated, stored and sent to the workstation. The length of the preset time period can be set as needed, and is preferably 36 seconds in this embodiment.

After the first alarm information is output, the record of the first alarm information is displayed in the event list column on the user interface of the multi-parameter monitor. When the user clicks the record through an operable device such as a touch screen or a mouse, the multi-parameter monitor receives Go to the first alarm information review command; at this time, according to the clicked record corresponding to the first alarm information, and according to the abnormal event record data and the first alarm information associated information query to obtain the first alarm information associated with the abnormal event record data.

In this solution, the abnormal event record data can also be analyzed and processed to generate and output abnormal event report data. The report data output abnormal event and the detailed description of the abnormal event may include, but are not limited to, each abnormal parameter, the occurrence time, the analysis result based on the abnormal parameter, and the like, and the data may be played in a graphical manner, such as electrocardiogram data. Graphical playback and so on.

Similarly, when the second alarm information is generated, the parameters before and after the generation of the second alarm information may be recorded in the same manner for convenient analysis and judgment, and details are not described herein again.

Further, comprehensively considering various parameters such as electrocardiogram data, pulse data, blood pressure data, respiratory data, blood oxygen saturation data, and body temperature data, and generating alarm event data according to the first alarm information and the second alarm information, and then according to The alarm time information is output and displayed on the alarm event data; the alarm event data includes the item information of the vital sign monitoring data and the corresponding ECG abnormal event information and/or other abnormal event information.

6 is a schematic structural diagram of a multi-parameter monitoring system according to an embodiment of the present invention, the multi-parameter monitoring system includes: at least one monitor 1 and a workstation 2;

The monitor 1 includes a memory 11 and a processor 12; the memory 11 can be connected to the processor 12 via a bus 13. The memory 11 may be a nonvolatile memory such as a hard disk drive and a flash memory in which a software program and a device driver are stored. The software program can perform various functions of the above method provided by the embodiments of the present invention; the device driver can be a network and an interface driver. The processor 12 is configured to execute a software program, and when the software program is executed, the method provided by the embodiment of the present invention can be implemented.

It should be noted that the embodiment of the present invention further provides a computer readable storage medium. The computer readable storage medium stores a computer program, and when the computer program is executed by the processor, the method provided by the embodiment of the present invention can be implemented.

Embodiments of the present invention also provide a computer program product comprising instructions. When the computer program product runs on a computer, the processor is caused to perform the above method.

The multi-parameter monitoring data analysis method and the multi-parameter monitoring system provided by the above embodiments of the present invention can automatically, quickly and completely perform the physical data such as electrocardiogram, blood pressure, blood oxygen, pulse, respiration, body temperature and the like monitored by the multi-parameter monitor. Analysis, giving an early warning of abnormal ECG status, abnormal parameters of other signs, and a combination of the two, and uploading to the workstation. It can reduce the false alarm caused by interference. The alarm accuracy is high, and the types of abnormalities that can be detected are especially the types of abnormalities of the electrocardiogram, and the ECG data can be dynamically played back and output according to the instructions. The multi-parameter monitoring data analysis method and multi-parameter monitoring system of the invention have wide application range and good application prospect.

In the above embodiment, the primary data processing of multi-parameter monitoring data analysis is implemented in a multi-parameter monitor. In the following embodiments, the primary data processing of multi-parameter monitoring data analysis is performed by the workstation.

Correspondingly, the present invention provides another multi-parameter monitoring data analysis method in the second embodiment. The method step flow is shown in FIG. 7 , and the method mainly includes the following steps:

Step 210: The monitor performs physical sign monitoring data collection on the measured object, obtains the vital sign monitoring data of the measured object, and acquires the measured object information, and sends the physical sign monitoring data and the measured object information to the workstation;

Specifically, the object to be measured refers to a living body that is monitored by a multi-parameter monitor, wherein the most conventional object to be measured refers to a person. The measured object information may specifically be information such as the name of the testee, the patient ID, the bed number, and the like, and must have information capable of uniquely identifying the identity of the user.

The monitor has a vital sign signal collecting device such as an electrode, a probe, a cuff, and the like, which is in contact with the object to be measured, and collects a vital sign signal of the measured object through the sign signal collecting device, and obtains the vital sign monitoring data through digital processing. The vital signs monitoring data may specifically include: electrocardiogram data, pulse data, blood pressure data, respiratory data, blood oxygen saturation data, and body temperature data. The vitality monitoring data has time attribute information, and each data point has a corresponding data collection time, which is time attribute information. At the same time as data acquisition, this data acquisition time is also recorded and stored as time attribute information of the vitals monitoring data. The vital sign monitoring data also has monitor ID information. When the physical monitoring data is collected, the information of the monitor for collecting the data, that is, the monitor ID information, is simultaneously recorded in the collected vital sign monitoring data.

The monitor monitoring data obtained by the monitor in real time is sent to the workstation by wired or wireless means mentioned in the above embodiments.

Step 220: The workstation determines monitoring reference data according to the measured object information.

Specifically, the monitoring reference data includes a vital sign data threshold and an electrocardiographic abnormal event information corresponding to the measured object information.

The workstation acquires monitoring reference data corresponding to the measured object according to the information of the measured object.

For example, the subject information is a patient ID, and according to the patient ID, it is determined that the subject is a newborn, and the monitoring reference data of the newborn is acquired.

Monitoring baseline data can be stored in a network data storage device connected to a workstation or workstation by a predetermined method.

The process of determining the detection reference data may also be performed in synchronization with step 230 below, or after step 230.

Step 230: The workstation performs wave group feature recognition on the electrocardiogram data, obtains a characteristic signal of the electrocardiogram data, performs heartbeat classification on the electrocardiogram data according to the characteristic signal, obtains heartbeat classification information according to the basic rule reference data of the electrocardiogram, and generates ECG event data;

Specifically, the processing procedure of the electrocardiogram data performed by the workstation is the same as the processing procedure of the electrocardiogram data performed by the monitor in the first embodiment, but the execution subject is different, and the specific procedure may refer to step 120 of the previous embodiment, and the specification. Figure 2 will not be repeated here. The resulting ECG event data includes monitor ID information.

Step 240: The workstation determines corresponding ECG event information according to the ECG event data, and determines whether the ECG event information is a preset ECG abnormal event information;

Specifically, the workstation can determine the ECG event information corresponding to the different ECG events according to the ECG event data, for example, the event information corresponding to the ECG event, or the event information further summarized based on the ECG event, for example, various conduction resistances. The stagnation event is classified as an abnormal event under the information of the conduction block event.

When the ECG event data determines that the corresponding ECG event information is the preset ECG abnormal event information, step 250 is performed. If the ECG event data determines that the corresponding ECG event information is not the preset ECG abnormal event information, it indicates that there is no abnormal ECG condition that needs to generate an alarm, and the monitoring of Step 210 continues.

Step 250, generating first alarm information;

Specifically, when the ECG event data determines that the corresponding ECG event information is preset ECG abnormal event information, the first alarm information is generated and output.

The first alarm information refers to the alarm information of the abnormality of the electrocardiogram, including the information of the abnormality of the electrocardiogram and the information of the alarm time and the ID of the monitor. Therefore, the first alarm information is generated based on the ECG abnormal event information and the alarm time information. The alarm time information may further be information about the time when the electrocardiographic abnormal event occurs, that is, the time information obtained from the time attribute information, or may be the information that the ECG event information is determined to be the preset ECG abnormal event information after processing the electrocardiogram data. System time information.

In order to distinguish different parameters, the ECG abnormal event information has corresponding project information, that is, an ECG project, which can indicate that the abnormal event is an ECG event.

The type of alarm that can generate the alarm information output according to the present invention can be seen in the specific example in step 140 in the foregoing embodiment.

Step 260: The workstation determines whether one or more of pulse data, blood pressure data, respiratory data, blood oxygen saturation data, and body temperature data have abnormal data exceeding a corresponding set threshold, and generates other abnormal event information according to the abnormal data;

In the process of actual data processing, step 260 and steps 220 and 230 may be performed in parallel, or in any order, without strict sequence between the two.

Specifically, for the pulse data, the blood pressure data, the respiratory data, the blood oxygen saturation data, and the body temperature data, the corresponding parameter threshold is determined by selecting the monitoring reference data.

When one or more of the above-mentioned vitality monitoring data exceeds the set parameter threshold, step 270 is performed; otherwise, step 210 is continued to continue the vital sign detection.

Step 270: The workstation generates other abnormal event information according to the abnormal data, and outputs the second alarm information.

Specifically, when the pulse data, the blood pressure data, the respiratory data, the blood oxygen saturation data, and the body temperature data have data exceeding a range of the corresponding set parameter, other abnormal event information is generated according to the specific excess. The other abnormal event information has corresponding item information, which is used to indicate which item has abnormal data. Such as pulse, blood pressure, breathing, blood oxygen or body temperature.

The second alarm information refers to the alarm information of the above other abnormal events except the abnormality of the electrocardiogram, including other abnormal event information and alarm time information. Therefore, the second alarm information is generated based on other abnormal event information and alarm time information. The alarm time information may further be information about the time when other abnormal events occur, that is, the time information obtained from the time attribute information, or may be determined by processing other vital signs data other than the electrocardiogram data to determine other abnormalities in the monitoring data. Information about the system time of the event. The second alarm information includes other abnormal event information, alarm time information, and monitor ID information.

Step 280, the workstation outputs the first alarm information and/or the second alarm information, and/or sends the first alarm information and/or the second alarm information to the monitor according to the monitor ID information, so that the monitor according to the first alarm information And/or the second alarm message generates a corresponding alarm output signal.

Specifically, after generating the first alarm information or the second alarm information, the workstation sends the alarm information to the corresponding monitor according to the monitor ID information, in addition to outputting the corresponding alarm information on the workstation side. In addition to the alarm information, it may include data before and after the alarm occurs, which will be described later. Thereby, the synchronous alarm output of the workstation and the monitor can be realized, so that the workstation and the monitor can synchronously receive the alarm information, so that the medical staff near the monitor can immediately receive the alarm, which greatly improves the response speed. In addition, other user equipment connected by the workstation, such as an alarm information receiving terminal carried by the doctor, can also synchronously receive the alarm information distributed by the workstation, thereby automatically realizing the synchronous distribution of the alarm information, thereby achieving a quick response effect.

In addition, the multi-parameter monitoring data analysis method of the present invention can also record data before and after the occurrence of an abnormal event, so that the abnormality analysis can be conveniently performed.

To this end, the workstation aggregates the vitality monitoring data according to the time attribute information of the vital sign monitoring data, generates time series data of the vital sign monitoring data, and stores it.

When it is determined that an abnormal event corresponding to the preset ECG abnormal event information occurs, the workstation acquires the ECG data in the preset time period before and after the corresponding time of the ECG data according to the time attribute information, and generates an abnormal event record data; The abnormal event records data associated with the first alarm information and stores it. For the second alarm information, the associated information can also be generated in the same manner.

After outputting the first alarm information or the second alarm information, the workstation receives the reference instruction for the first alarm information or the second alarm information, acquires corresponding abnormal event record data, and outputs the data.

Specifically, the lookup instruction may be initiated on the workstation side or on the side of the monitor. For example, after the first alarm information is output, the record of the first alarm information is displayed in the event list column on the user interface of the multi-parameter monitor. When the user clicks the record through an operable device such as a touch screen or a mouse, multi-parameter monitoring The instrument generates a reference instruction of the first alarm information, and sends the instruction to the workstation; the workstation determines the first alarm information according to the reference instruction of the first alarm information, and queries and obtains the information according to the abnormal event record data and the first alarm information. The abnormal event record data associated with the first alarm information.

In this solution, the abnormal event record data can also be analyzed and processed, and abnormal event report data is generated and output. The report data output abnormal event and the detailed description of the abnormal event may include, but are not limited to, each abnormal parameter, the occurrence time, the analysis result based on the abnormal parameter, and the like, and the data may be played in a graphical manner, such as electrocardiogram data. Graphical playback and so on.

Similarly, when the second alarm information is generated, the parameters before and after the generation of the second alarm information may be recorded in the same manner for convenient analysis and judgment, and details are not described herein again.

Further, comprehensively considering various parameters such as electrocardiogram data, pulse data, blood pressure data, respiratory data, blood oxygen saturation data, and body temperature data, and generating alarm event data according to the first alarm information and the second alarm information, and then according to The alarm time information is output and displayed on the alarm event data; the alarm event data includes the item information of the vital sign monitoring data and the corresponding ECG abnormal event information and/or other abnormal event information.

FIG. 8 is a schematic structural diagram of a multi-parameter monitoring system according to an embodiment of the present invention, the multi-parameter monitoring system includes: at least one monitor 2 and a workstation 1;

The workstation 1 includes a memory 11 and a processor 12; the memory 11 can be connected to the processor 12 via a bus 13. The memory 11 may be a nonvolatile memory such as a hard disk drive and a flash memory in which a software program and a device driver are stored. The software program can perform various functions of the above method provided by the embodiments of the present invention; the device driver can be a network and an interface driver. The processor 12 is configured to execute a software program, and when the software program is executed, the method provided by the embodiment of the present invention can be implemented.

It should be noted that the embodiment of the present invention further provides a computer readable storage medium. The computer readable storage medium stores a computer program, and when the computer program is executed by the processor, the method provided by the embodiment of the present invention can be implemented.

Embodiments of the present invention also provide a computer program product comprising instructions. When the computer program product runs on a computer, the processor is caused to perform the above method.

The multi-parameter monitoring data analysis method and the multi-parameter monitoring system provided by the above embodiments of the present invention can automatically perform physical data such as electrocardiogram, blood pressure, blood oxygen, pulse, respiration, body temperature and the like monitored and uploaded by the multi-parameter monitor. Fast and complete analysis, giving an early warning to the abnormal ECG status, abnormal parameters of other signs, and the combination of the two, and issued to the monitor for synchronous alarm output. This method can reduce the false alarm phenomenon caused by interference. The alarm accuracy is high, and the types of abnormalities that can be detected are especially the types of abnormalities of the electrocardiogram, and the ECG data can be dynamically played back and output according to the instructions. The multi-parameter monitoring data analysis method and multi-parameter monitoring system of the invention have wide application range and good application prospect.

A person skilled in the art should further appreciate that the elements and algorithm steps of the various examples described in connection with the embodiments disclosed herein can be implemented in electronic hardware, computer software, or a combination of both, in order to clearly illustrate hardware and software. Interchangeability, the composition and steps of the various examples have been generally described in terms of function in the above description. Whether these functions are performed in hardware or software depends on the specific application and design constraints of the solution. A person skilled in the art can use different methods for implementing the described functions for each particular application, but such implementation should not be considered to be beyond the scope of the present invention.

The steps of a method or algorithm described in connection with the embodiments disclosed herein can be implemented in hardware, a software module executed by a processor, or a combination of both. The software module can be placed in random access memory (RAM), memory, read only memory (ROM), electrically programmable ROM, electrically erasable programmable ROM, registers, hard disk, removable disk, CD-ROM, or technical field. Any other form of storage medium known.

The specific embodiments of the present invention have been described in detail with reference to the preferred embodiments of the present invention. All modifications, equivalent substitutions, improvements, etc., made within the spirit and scope of the invention are intended to be included within the scope of the invention.

Claims (17)

1. A multi-parameter monitoring data analysis method, the method comprising:

   The monitoring device receives the monitoring reference data input by the user or sent by the workstation; the monitoring reference data includes the measured object information, and the physical data threshold and the electrocardiographic abnormal event information corresponding to the measured object information;

   The monitor performs physical sign monitoring data collection on the measured object to obtain the vital sign monitoring data of the measured object; the vital sign monitoring data has time attribute information and monitor ID information, and the vital sign monitoring data includes: electrocardiogram data, Pulse data, blood pressure data, respiratory data, blood oxygen saturation data, and body temperature data;

   The monitor performs wave group feature recognition on the electrocardiogram data, obtains a characteristic signal of the electrocardiogram data, performs heartbeat classification on the electrocardiogram data according to the feature signal, and obtains heartbeat classification information according to the basic rule reference data of the electrocardiogram And generating electrocardiogram event data; the ECG event data including the monitor ID information;

   The monitor determines corresponding ECG event information according to the ECG event data, and determines whether the ECG event information is the ECG abnormal event information; when the ECG abnormal event information is, outputting the first alarm information The first alarm information includes the ECG abnormal event information, alarm time information, and the monitor ID information;

   Determining, by the monitor, one or more of the pulse data, blood pressure data, respiratory data, blood oxygen saturation data, and body temperature data whether there is abnormal data exceeding a corresponding set threshold, and generating other according to the abnormal data The abnormal event information; when the set threshold is exceeded, outputting the second alarm information; the second alarm information includes the other abnormal event information, the alarm time information, and the monitor ID information;

   The monitor sends the first alarm information and/or the second alarm information to a workstation, so that the workstation generates a corresponding alarm output signal according to the first alarm information and/or the second alarm information. .
2. The multi-parameter monitoring data analysis method according to claim 1, wherein the method further comprises:

   The monitor aggregates the vital sign monitoring data according to the time attribute information of the vital sign monitoring data, generates time series data of the vital sign monitoring data, and stores the time series data.
3. The multi-parameter monitoring data analysis method according to claim 1, wherein the method further comprises:

   When the preset ECG abnormal event information is obtained, the ECG data in the preset time period before and after the corresponding time of the ECG data is acquired according to the time attribute information, and the abnormal event record data is generated;

   The monitor generates association information of the abnormal event record data and the first alarm information, and sends the information to the workstation.
4. The method of analyzing a multi-parameter monitoring data according to claim 3, wherein the method further comprises:

   Receiving, by the monitor or the workstation, a reference instruction for the first alarm information or the second alarm information, acquiring corresponding abnormal event record data, and outputting, and/or analyzing and processing the abnormal event record data, Generate and output exception event report data.
5. The multi-parameter monitoring data analysis method according to claim 1, wherein the electrocardiographic data is subjected to wave group feature recognition to obtain a characteristic signal of the electrocardiogram data, and the electrocardiogram data is obtained according to the characteristic signal. Perform heartbeat classification, combine heartbeat basic rule reference data to obtain heartbeat classification information, and generate ECG event data specifically including:

   Converting the data format of the electrocardiogram data into a preset standard data format by performing re-sampling, and performing first filtering processing on the ECG data of the converted preset standard data format;

   Performing a heartbeat detection process on the electrocardiogram data after the first filtering process, and identifying a plurality of heartbeat data included in the electrocardiogram data, each of the heartbeat data corresponding to one heart cycle, including a corresponding P wave, QRS Wave group, T wave amplitude and start and end time data;

   Determining a confidence level of each heartbeat based on the heartbeat data;

   Performing interference recognition on the heartbeat data according to the interference recognition two-class classification model, obtaining whether the heartbeat data has interference noise, and a probability value for determining the interference noise;

   Determining the validity of the heartbeat data according to the detection confidence, and, according to the lead parameter and the heartbeat data determining the valid heartbeat data, combining the result of the interference recognition and the time rule to generate the heartbeat time series data; Generating heartbeat analysis data according to the heartbeat time series data;

   Performing feature extraction and analysis of the amplitude and time characterization data on the heartbeat analysis data according to a heartbeat classification model to obtain primary classification information of the cardiac analysis data;

   The heartbeat analysis data of the specific heartbeat in the primary classification information result is input to the ST segment and the T wave change model for identification, and the ST segment and T wave evaluation information is determined;

   Performing P wave and T wave feature detection on the heartbeat analysis data according to the heartbeat time series data, and determining detailed feature information of P wave and T wave in each heart beat, the detailed feature information includes amplitude, direction, Form and start and end time data;

   Performing secondary classification processing on the heartbeat analysis data according to the electrocardiogram basic rule reference data, the detailed feature information of the P wave and the T wave, and the ST segment and T wave evaluation information under the primary classification information, Get heartbeat classification information;

   The heartbeat classification information is analyzed and matched to generate the ECG event data.
6. A multi-parameter monitoring data analysis method, the method comprising:

   The monitor performs physical condition monitoring data collection on the measured object, obtains the vital sign monitoring data of the measured object, and acquires the measured object information, and sends the physical condition monitoring data and the measured object information to the workstation; The vital sign monitoring data has time attribute information and monitor ID information, and the vital sign monitoring data includes: electrocardiogram data, pulse data, blood pressure data, respiratory data, blood oxygen saturation data, and body temperature data;

   The workstation performs wave group feature recognition on the electrocardiogram data, obtains a characteristic signal of the electrocardiogram data, performs heartbeat classification on the electrocardiogram data according to the characteristic signal, and obtains heartbeat classification information according to the basic rule reference data of the electrocardiogram, And generating ECG event data; the ECG event data includes the monitor ID information;

   The workstation determines monitoring reference data according to the measured object information; the monitoring reference data includes a vital sign data threshold and an electrocardiographic abnormal event information corresponding to the measured object information;

   Determining, according to the electrocardiogram event data, the corresponding ECG event information, and determining whether the ECG event information is a preset ECG abnormal event information; and when the preset ECG abnormal event information is generated, generating a first alarm Information; the first alarm information includes the ECG abnormal event information, alarm time information, and the monitor ID information;

   The workstation determines whether one or more of the pulse data, blood pressure data, respiratory data, blood oxygen saturation data, and body temperature data have abnormal data exceeding a corresponding set threshold, and generates other abnormalities according to the abnormal data. Event information; when the set threshold is exceeded, generating second alarm information; the second alarm information includes the other abnormal event information, alarm time information, and the monitor ID information;

   The workstation outputs the first alarm information and/or the second alarm information, and sends the first alarm information and/or the second alarm information to the monitor according to the monitor ID information And causing the monitor to generate a corresponding alarm output signal according to the first alarm information and/or the second alarm information.
7. The method of analyzing a multi-parameter monitoring data according to claim 6, wherein the method further comprises:

   The workstation aggregates the vital sign monitoring data according to the time attribute information of the vital sign monitoring data, generates time series data of the vital sign monitoring data, and stores the time series data.
8. The method of analyzing a multi-parameter monitoring data according to claim 6, wherein the method further comprises:

   When it is the preset ECG abnormal event information, the workstation acquires the electrocardiogram data in the preset time period before and after the corresponding time of the ECG data according to the time attribute information, and generates abnormal event record data;

   The workstation generates association information of the abnormal event record data and the first alarm information.
9. The method of analyzing a multi-parameter monitoring data according to claim 8, wherein the method further comprises:

   Receiving, by the workstation, a reference instruction for the first alarm information or the second alarm information, acquiring corresponding abnormal event record data and outputting, and/or analyzing and processing the abnormal event record data, generating and outputting an abnormal event Report data.
10. The multi-parameter monitoring data analysis method according to claim 9, wherein the method further comprises:

    The monitor receives a review instruction for the first alarm information or the second alarm information;

    Sending the lookup instruction to the workstation;

    The workstation acquires the abnormal event record data, and/or analyzes and processes the abnormal event record data to generate abnormal event report data;

    The abnormal event record data and/or abnormal event report data is transmitted to the monitor.
11. The multi-parameter monitoring data analysis method according to claim 6, wherein the electrocardiographic data is subjected to wave group feature recognition to obtain a characteristic signal of the electrocardiogram data, and the electrocardiogram data is obtained according to the characteristic signal. Perform heartbeat classification, combine heartbeat basic rule reference data to obtain heartbeat classification information, and generate ECG event data specifically including:

    Converting the data format of the electrocardiogram data into a preset standard data format by performing re-sampling, and performing first filtering processing on the ECG data of the converted preset standard data format;

    Performing a heartbeat detection process on the electrocardiogram data after the first filtering process, and identifying a plurality of heartbeat data included in the electrocardiogram data, each of the heartbeat data corresponding to one heart cycle, including a corresponding P wave, QRS Wave group, T wave amplitude and start and end time data;

    Determining a confidence level of each heartbeat based on the heartbeat data;

    Performing interference recognition on the heartbeat data according to the interference recognition two-class classification model, obtaining whether the heartbeat data has interference noise, and a probability value for determining the interference noise;

    Determining the validity of the heartbeat data according to the detection confidence, and, according to the lead parameter and the heartbeat data determining the valid heartbeat data, combining the result of the interference recognition and the time rule to generate the heartbeat time series data; Generating heartbeat analysis data according to the heartbeat time series data;

    Performing feature extraction and analysis of the amplitude and time characterization data on the heartbeat analysis data according to a heartbeat classification model to obtain primary classification information of the cardiac analysis data;

    The heartbeat analysis data of the specific heartbeat in the primary classification information result is input to the ST segment and the T wave change model for identification, and the ST segment and T wave evaluation information is determined;

    Performing P wave and T wave feature detection on the heartbeat analysis data according to the heartbeat time series data, and determining detailed feature information of P wave and T wave in each heart beat, the detailed feature information includes amplitude, direction, Form and start and end time data;

    Performing secondary classification processing on the heartbeat analysis data according to the electrocardiogram basic rule reference data, the detailed feature information of the P wave and the T wave, and the ST segment and T wave evaluation information under the primary classification information, Get heartbeat classification information;

    The heartbeat classification information is analyzed and matched to generate the ECG event data.
12. A multi-parameter monitoring system, characterized in that the multi-parameter monitoring system comprises the monitor and workstation of any of claims 1-5;

    The monitor includes: a memory for storing a program, and a processor for performing the method of any one of claims 1 to 5.
13. A computer program product comprising instructions which, when run on a computer, cause the computer to perform the method of any one of claims 1 to 5.
14. A computer readable storage medium comprising instructions which, when executed on a computer, cause the computer to perform the method of any one of claims 1 to 5.
15. A multi-parameter monitoring system, comprising the workstation of any of claims 6-11 and one or more monitors;

    The workstation comprises: a memory for storing a program, the processor for performing the method of any one of claims 6 to 11.
16. A computer program product comprising instructions which, when run on a computer, cause the computer to perform the method of any one of claims 6 to 11.
17. A computer readable storage medium comprising instructions which, when executed on a computer, cause the computer to perform the method of any one of claims 6 to 11.

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