CN109541194B - Body detection system for detecting cerebral infarction - Google Patents
Body detection system for detecting cerebral infarction Download PDFInfo
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- CN109541194B CN109541194B CN201811273758.7A CN201811273758A CN109541194B CN 109541194 B CN109541194 B CN 109541194B CN 201811273758 A CN201811273758 A CN 201811273758A CN 109541194 B CN109541194 B CN 109541194B
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- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N33/00—Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
- G01N33/48—Biological material, e.g. blood, urine; Haemocytometers
- G01N33/50—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
- G01N33/5002—Partitioning blood components
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B5/00—Measuring for diagnostic purposes; Identification of persons
- A61B5/02—Detecting, measuring or recording pulse, heart rate, blood pressure or blood flow; Combined pulse/heart-rate/blood pressure determination; Evaluating a cardiovascular condition not otherwise provided for, e.g. using combinations of techniques provided for in this group with electrocardiography or electroauscultation; Heart catheters for measuring blood pressure
- A61B5/0205—Simultaneously evaluating both cardiovascular conditions and different types of body conditions, e.g. heart and respiratory condition
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- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N33/00—Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
- G01N33/48—Biological material, e.g. blood, urine; Haemocytometers
- G01N33/50—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
- G01N33/53—Immunoassay; Biospecific binding assay; Materials therefor
Abstract
The invention provides a body detection system for detecting cerebral infarction, comprising: the body detection device is used for detecting the physiological index of the user according to a preset detection period to obtain a detection result corresponding to each detection period; the monitoring server analyzes whether each physiological index in the detection result corresponding to each detection period falls into a preset physiological index or not; when a physiological index which does not fall into a preset physiological index exists, sending the physiological index which does not fall into the preset physiological index, a detection cycle identifier corresponding to the physiological index and a detection result to a monitoring terminal; the memorandum application is used for being used by the user, records the memorandum schedule of the user in each detection period, and sends the memorandum schedule corresponding to each detection period to the monitoring server; the monitoring server determines whether the same memo schedule with the repetition times exceeding the preset times exists according to the memo schedule corresponding to each detection period; and if so, sending the same memo schedule to the monitoring terminal.
Description
Technical Field
The invention relates to the technical field of data analysis, in particular to a body detection system for detecting cerebral infarction.
Background
At present, with the aging of the population of China becoming worse and the pace of life becoming faster, cerebral infarction has become a serious disease which harms China. Clinical application shows that the treatment is critical within 3 hours after cerebral infarction. Only when patients with cerebral infarction are subjected to early prevention, early discovery and early treatment, the lives of the patients can be saved to the maximum extent, and the prognosis of the patients can be improved to the maximum extent.
The current research shows that the human body is accompanied with the heart rate abnormality in the early stage of the attack of cerebral infarction, and the blood pressure and the blood oxygen have larger changes. However, the prior art lacks a monitoring technology which can be known in time when the physiological index of the user is abnormal, and the monitoring technology is generally manual, so that the efficiency is low, and more manpower is occupied.
Disclosure of Invention
In order to solve the above technical problems, the present invention provides a body detection system for detecting a cerebral infarction, so as to provide a technology that can be known in time when an abnormality occurs in a physiological index of a user.
The embodiment of the invention provides a body detection system for detecting cerebral infarction, which comprises:
the body detection device is used for detecting the physiological index of the user according to a preset detection period to obtain a detection result corresponding to each detection period;
the monitoring server is used for analyzing whether each physiological index in the detection result corresponding to each detection period falls into a preset physiological index or not; when a physiological index which does not fall into a preset physiological index exists, sending the physiological index which does not fall into the preset physiological index, a detection cycle identifier corresponding to the physiological index and a detection result to a monitoring terminal;
the memo application is used for the user to use and is used for recording the memo schedule of the user in each detection period and sending the memo schedule corresponding to each detection period to the monitoring server;
the monitoring server is also used for determining whether the same memo schedule with the repetition times exceeding the preset times exists according to the memo schedule corresponding to each detection period; and if so, sending the same memo schedule to the monitoring terminal.
In one embodiment, the body detection device further comprises a blood routine biochemical detection module;
the blood routine biochemical detection module comprises a blood routine detection unit, a transmission unit, a biochemical detection unit and a control component;
the transmission unit comprises a blood drawing component, the blood drawing component is respectively connected with the conventional blood detection unit and the biochemical detection unit, and the blood drawing component is used for transmitting the blood sample drawn in the conventional blood detection unit to the biochemical detection unit;
the control assembly is connected with the blood routine detection unit, the transmission unit and the biochemical detection unit and is used for controlling the blood routine biochemical detection module;
the transmission unit further comprises a first control switch, a second control switch and a blood discharge assembly, one end of the blood drawing assembly is connected with the conventional blood detection unit through the first control switch, the other end of the blood drawing assembly is connected with the blood discharge assembly through the second control switch, and the blood discharge assembly is connected with the biochemical detection unit; when the first control switch is turned on and the second control switch is turned off, the blood drawing assembly draws the blood sample output by the conventional blood detection unit; when the first control switch is closed and the second control switch is opened, the blood drawing component transmits the drawn blood sample to the biochemical detection unit;
the blood routine detecting unit, the biochemical detecting unit, the control component and the processing module, and the processing module receives the detection information of the blood routine detecting unit and the biochemical detecting unit.
A blood immunoassay module including a blood lysing unit, a first illumination device, a first light receiving device, a first analyzing device, a blood reagent unit, a second illumination device, a second light receiving device, and a second analyzing device;
a blood lysing unit for adding a blood lysing agent to the blood sample;
a first illumination device for illuminating a first blood sample, the first blood sample being a blood sample to which a blood lysing agent is added;
a first light receiving device for receiving the light emitted from the first illuminating device and transmitted through the first blood sample and detecting the intensity of the light received by the first blood sample;
a first analysis device for obtaining the concentration of hemoglobin in the blood sample based on the intensity of light received by the first blood sample;
a blood reagent unit for adding an immunological reagent to the first blood sample;
a second illumination device for illuminating a second blood sample, the second blood sample being the first blood sample to which the immunoreagent is added;
a second light receiving means for receiving light emitted from the second illuminating means and transmitted through the second blood sample and detecting intensity of illumination received by the second blood sample;
a second analysis device for analyzing the substance concentration of the obtained blood sample according to the intensity of the light received by the second blood sample and the hemoglobin concentration of the blood sample obtained by the first analysis device;
the blood immunity detection module is connected with the processing module and is used for transmitting the detection information acquired by the blood immunity detection module to the processing module;
the processing module is used for transmitting the received blood immunity detection information, the blood conventional biochemical detection information and the cerebral infarction detection information to the monitoring server through an encryption algorithm;
and the monitoring server decrypts the transmitted detection information according to the key of the preset encryption algorithm to acquire the detection information.
In an embodiment, the monitoring server is further configured to analyze the potential risk of the cerebral infarction of the user according to the detection result corresponding to each detection period and a preset cerebral infarction diagnosis model.
In one embodiment, the body detection device comprises a bracelet, on which a physiological index detection component is disposed, the physiological index detection component comprising any one or more of a heart rate detection component, a pulse detection component, a blood oxygen value detection component, and a blood pressure detection component.
In one embodiment, the bracelet includes two wristbands and a bracelet body 31 disposed between the two wristbands; the first bracelet 32 of the two bracelets is longer than the second bracelet 33;
the first wrist strap 32 has an accommodating space 33 therein, and the accommodating space 33 is communicated with the outside through a hole on the first wrist strap 32; a bendable plate-like body 34, the plate-like body 34 being movably disposed in the accommodating space 33 and being detachable from the wrist band through the hole; a data plug 35 is arranged at one end of the plate-shaped body 34 close to the connecting end of the first wrist strap 32 and the first wrist strap 31, and a data jack 36 matched with the data plug 35 is arranged at one end of the first wrist strap 31 connected with the first wrist strap 32; a plurality of placing grooves 37 are formed in the inner surface of the plate-shaped body 34, a physiological index detecting assembly 38 is placed in each placing groove 37, and each physiological index detecting assembly 38 is connected with the data plug 35 through a data line arranged in the plate-shaped body 34; the plate-shaped body 34 is also provided with a button battery 36, and the button battery 36 is connected with each physiological index detection assembly 38; when the plate-shaped body 34 is placed in the first wrist strap 32, the data plug 35 is plugged into the data jack 36, and the inner surface of the first wrist strap 32 is provided with an opening matched with the physiological index detection component 38, so that when the wrist wears a bracelet, and the first wrist strap 32 is worn on the wrist, the physiological index detection component 38 can also be contacted with the skin of the wrist, thereby achieving the purpose of detection;
one end of the first wrist strap 32 away from the main body of the wrist strap is connected to a first elastic strap 39, and the first elastic strap 39 is provided with a buckle connector 310. One end of the second wrist strap 33 far from the main body of the wrist strap is connected to a second elastic strap 311, and a fastening hole 312 adapted to the fastening head 310 is disposed on the second elastic strap 311.
In one embodiment, the analyzing the potential risk of the cerebral infarction of the user according to the detection result corresponding to each detection cycle and a preset cerebral infarction diagnosis model includes:
step 1: acquiring detection results corresponding to N1 continuous detection periods from the body detection device to obtain N1 detection results; determining whether the N1 is equal to or greater than N; if yes, continuing to step 2; otherwise, ending the flow;
step 2: determining the number of a first group of detection results of which the blood pressure value is greater than a preset blood pressure value from the N1 detection results; continuing to step 3 when the number of the first set of detection results is equal to or greater than N2; when the number of the first group of detection results is less than N2, deleting the N1 detection results, and reusing the body detection device for detection;
and step 3: when the number of the first group of detection results is equal to or larger than N2, judging whether the detection period corresponding to each detection result in the first group of detection results is adjacent; when not adjacent, returning to the step 1; when adjacent, continuing to step 4;
and 4, step 4: when the detection periods corresponding to each detection result in the first group of detection results are adjacent, determining the number of the second group of detection results when the organ of the user is in the sub-health state according to the N1 detection results; judging whether the number of the second group of detection results is equal to or larger than N3; when the number of the second group of detection results is equal to or greater than N3, recording the first organ in the sub-health state, and continuing to the step 5;
and 5: determining a second organ with a blood oxygen value equal to or less than a preset blood oxygen value from the N1 test results; judging the number of detection results that the blood oxygen value of the second organ is equal to or less than a preset blood oxygen value; when the number is equal to or greater than N4, recording a second organ, and continuing with step 6; when the number is less than N4 and greater than 1, returning to the step 5; when the number is equal to 0, ending the flow;
step 6: and taking the first organ, the second organ, the first group of detection results and the second group of detection results as a basis for judging whether the user has a potential cerebral infarction risk, and analyzing the potential cerebral infarction risk of the user by combining a preset cerebral infarction diagnosis model to generate an analysis report.
In one embodiment, the preset cerebral infarction diagnosis model at least comprises a value range of a physiological index of a preset organ of a cerebral infarction potential patient;
the step 6 includes:
judging whether the first organ and the second organ contain the preset organ or not;
when the first organ and the second organ contain the preset organ, judging whether the physiological index corresponding to the first organ in the first group of detection results is located in a value range of the physiological index corresponding to the first organ and judging whether the physiological index corresponding to the second organ in the second group of detection results is located in a value range of the physiological index corresponding to the second organ; when the two judgment results are yes, generating a report that the user is a potential cerebral infarction patient; when at least one of the two judgment results is negative, generating a report that the user is not a potential cerebral infarction patient;
generating a report that the user is not a potential patient for cerebral infarction when the predetermined organ is not included in the first and second organs.
In one embodiment, the system further comprises a user information collecting module for collecting user information of the user, wherein the user information comprises gender and age;
the monitoring server is further configured to send the user information of the user, the physiological index that does not fall within the preset physiological index, and the detection cycle identifier and the detection result corresponding to the physiological index to the monitoring terminal.
In one embodiment, the analyzing, by the monitoring server, the potential risk of the brainstem of the user according to the detection result corresponding to each detection cycle and a preset brainstem diagnosis model includes:
the monitoring server acquires a matching model matched with the gender and the age of the user from a preset cerebral infarction diagnosis model according to the gender and the age of the user;
and analyzing the potential risk of the cerebral infarction of the user according to the detection result corresponding to each detection period and the matching model.
In one embodiment, further comprising:
the client is in communication connection with the monitoring server and used for acquiring an analysis result obtained after the monitoring server analyzes the potential risk of the cerebral infarction of the user and displaying the analysis result to the user;
and the monitoring server is further used for sending the analysis result to the client when the analysis result obtained after the analysis of the potential risk of the cerebral infarction of the user is a preset result.
Additional features and advantages of the invention will be set forth in the description which follows, and in part will be obvious from the description, or may be learned by practice of the invention. The objectives and other advantages of the invention will be realized and attained by the structure particularly pointed out in the written description and claims hereof as well as the appended drawings.
The technical solution of the present invention is further described in detail by the accompanying drawings and embodiments.
Drawings
FIG. 1 is a block diagram of a body detection system for cerebral infarction detection according to the present invention;
FIG. 2 is a flow chart of a process of a monitoring server provided by the present invention;
fig. 3 is a schematic view of a bracelet structure of a body detection system for detecting a cerebral infarction according to the present invention;
fig. 4 is a schematic structural view of a back cover of a bracelet of the body detection system for detecting the cerebral infarction provided by the invention;
fig. 5 is a schematic side view of a back cover of a bracelet of the body detection system for detecting a cerebral infarction provided by the invention.
Detailed Description
The preferred embodiments of the present invention will be described in conjunction with the accompanying drawings, and it will be understood that they are described herein for the purpose of illustration and explanation and not limitation.
According to the technical scheme, the long-term physiological trend is judged mainly through big data by using the pulse wave theory of the traditional Chinese medicine according to the acquired physiological data such as heart rate, blood pressure and blood oxygen data and the personal information of a user such as sex and age. The cerebral infarction diagnosis model judges the physiological change corresponding to each time through midnight-noon ebb-flow of the internal meridian of the yellow emperor in traditional Chinese medicine to judge the real-time state of organs, judges clinical symptoms according to the real-time physiological change, such as prediction of cerebral infarction risks, and can provide cerebral infarction risk prompts for users in advance.
An embodiment of the present invention provides a body detection system for detecting a cerebral infarction, as shown in fig. 1, including:
the body detection device 11 is used for detecting the physiological index of the user according to a preset detection period to obtain a detection result corresponding to each detection period; wherein the physiological index can be any one or more of heart rate, pulse, blood oxygen value and blood pressure.
The monitoring server 12 is configured to analyze whether each physiological index in the detection result corresponding to each detection period falls within a preset physiological index; when a physiological index which does not fall into a preset physiological index exists, sending the physiological index which does not fall into the preset physiological index, a detection cycle identifier corresponding to the physiological index and a detection result to a monitoring terminal;
the memo application 13 is used by the user to record a memo schedule of the user in each detection period and send the memo schedule corresponding to each detection period to the monitoring server;
the monitoring server 12 is further configured to determine whether the same memo schedule with the repetition times exceeding the preset times exists according to the memo schedule corresponding to each detection period; and if so, sending the same memo schedule to the monitoring terminal.
Wherein, determining whether the same memo schedule with the repetition times exceeding the preset times exists according to the memo schedule corresponding to each detection period can be implemented as follows: and judging whether a memo schedule exists in each detection period, wherein the memo schedule repeatedly appears in the detection period, for example, when the detection period is in days, the number of times of the memo schedule of 'paying electricity charge' appearing in the memo schedule of the first day exceeds 2, and the memo schedule of 'paying electricity charge' belongs to the same memo schedule. Or, it may be that whether a memo schedule exists in a plurality of detection periods, and the memo schedule appears in the plurality of detection periods, for example, if a memo schedule of "buy water pipe" appears in a memo schedule of five days, and the number of times of the memo schedule of "buy water pipe" appears in the five days exceeds 10 times, then the memo schedule of "buy water pipe" belongs to the same memo schedule.
The system can be timely known when the physiological index of the user is abnormal, the body of the user can be conveniently monitored, whether the physiological index exceeds the standard or not does not need to be manually checked, the labor is saved, and the monitoring efficiency is improved. In addition, the brainstem patients are frequently forgotten in the past, so the method and the system analyze whether the users frequently use the memorandum application to record the same schedule or not by using the information recorded by the memorandum application, and if the times of recording the same schedule exceed a certain number, the monitoring server sends the schedule to the monitoring terminal. The management personnel (such as doctors) of the monitoring terminal can preliminarily judge whether the user has potential cerebral infarction risks according to the information sent by the monitoring server, and therefore the system assists the doctors to diagnose and treat the patients and provides a plurality of basis for diagnosis and treatment.
In one embodiment, the monitoring server may further analyze the importance degree of the same memo schedule, wherein the memo application may send the same memo schedule together with the importance degree to the monitoring server according to the importance degree corresponding to each memo schedule at the setting mark of the user. The monitoring server scores the same memo schedule according to the importance degree of the same memo schedule and the overrun times (the value obtained by subtracting the preset times from the occurrence times of the same memo schedule) that the same memo schedule exceeds the preset times, and the scoring formula is as follows: q ═ Z × N, where Q is the final score for the same memo schedule; z is the weight corresponding to the importance degree of the same memo schedule, the higher the importance degree is, the larger the weight is, and the specific weight value can be set by self; and N is the number of the overrun times. The monitoring server sends the scoring value corresponding to the same memo schedule, the same memo schedule and the overrun times to the monitoring terminal so as to provide richer diagnosis and treatment basis for managers (such as doctors) of the monitoring terminal.
In one embodiment, the monitoring server is further configured to analyze the potential risk of the cerebral infarction of the user according to the detection result corresponding to each detection period and a preset cerebral infarction diagnosis model.
In one embodiment, the body detection device may be implemented as a bracelet, on which the physiological index detection component is disposed, and the physiological index detection component includes any one or more of a heart rate detection component, a pulse detection component, a blood oxygen value detection component, and a blood pressure detection component. Other body detection devices are also possible, as long as the physiological index of the user can be detected, and the invention is not limited.
In an embodiment, the monitoring server analyzes the potential risk of the cerebral infarction of the user according to the detection result corresponding to each detection period and a preset cerebral infarction diagnosis model, as shown in fig. 2, the following steps 1 to 6 may be implemented:
step 1: acquiring detection results corresponding to N1 continuous detection periods from a body detection device to obtain N1 detection results; determining whether N1 is equal to or greater than N; if yes, continuing to step 2; otherwise, ending the flow;
the detection period may be calculated by day, for example, one detection period per day. Preferably, N may be a value set in advance such as 14, 21, 35, etc., preferably 21; n1 is preferably also 21, i.e. 21 days of detection can be obtained in step 1. When a certain number of detection results are available, the detection results can be used as an effective basis for subsequent prediction diagnosis, and if the number of the detection results is insufficient, the user is continuously detected.
Step 2: determining the number of the first group of detection results of which the blood pressure value is greater than the preset blood pressure value from the N1 detection results;
continuing to step 3 when the number of the first set of detection results is equal to or greater than N2;
and when the number of the first group of detection results is less than N2, deleting N1 detection results and reusing the body detection device for detection.
Among them, when N1 is equal to 21, N2 is preferably 7.
If the blood pressure value is larger than the preset blood pressure value, the blood pressure of the user is abnormal, and when more blood pressures in the detection result are abnormal, the subsequent step 3 needs to be continuously executed for prediction; when the abnormal blood pressure is less, the user is healthy, and the body of the user can be continuously detected.
And step 3: when the number of the first group of detection results is equal to or larger than N2, judging whether the detection period corresponding to each detection result in the first group of detection results is adjacent; when not adjacent, returning to the step 1; when adjacent, continue step 4.
That is, when the abnormal blood pressure condition of the user continuously appears, it indicates that the body of the user may have a problem, and the prediction needs to be continued to the subsequent step 4. When the abnormal condition of the blood pressure of the user is not continuous, the body of the user is indicated to have no big obstacle, and the body detection of the user is continued.
And 4, step 4: when the detection periods corresponding to each detection result in the first group of detection results are adjacent, determining the number of the second group of detection results of the sub-health state of the organ of the user according to the N1 detection results; judging whether the number of the second group of detection results is equal to or larger than N3;
when the number of second set of test results is equal to or greater than N3, the first organ in sub-health state is recorded and step 5 is continued.
Wherein preferably N3 is 15.
And 5: determining a second organ having a blood oxygen value equal to or less than a predetermined blood oxygen value from the N1 test results; and judging the number of detection results that the blood oxygen value of the second organ is equal to or less than the preset blood oxygen value; when the number is equal to or greater than N4, recording a second organ, and continuing with step 6; when the number is less than N4 and greater than 1, returning to the step 5; when the number is equal to 0, the flow ends.
Wherein preferably N4 is 10.
Step 6: and (3) taking the first organ, the second organ, the first group of detection results and the second group of detection results as a basis for judging whether the user has a potential cerebral infarction risk, analyzing the potential cerebral infarction risk of the user by combining a preset cerebral infarction diagnosis model, and generating an analysis report.
The system provided by the embodiment of the invention can predict the potential cerebral infarction risk of the user according to the body detection result, and compared with the prior art which needs artificial prediction, the system provides an intelligent auxiliary means, has scientific basis, can ensure the prediction accuracy, and can timely evaluate the cerebral infarction risk of the user.
In one embodiment, the preset cerebral infarction diagnosis model at least comprises a value range of a physiological index of a preset organ of a cerebral infarction potential patient;
and step 6, comprising:
judging whether the first organ and the second organ contain a preset organ or not;
when the first organ and the second organ contain preset organs, judging whether the physiological index corresponding to the first organ in the first group of detection results is located in the value range of the physiological index corresponding to the first organ and judging whether the physiological index corresponding to the second organ in the second group of detection results is located in the value range of the physiological index corresponding to the second organ; when the two judgment results are yes, generating a report that the user is a potential patient with cerebral infarction; when at least one of the two judgment results is negative, generating a report that the user is not a potential patient with cerebral infarction;
when the preset organ is not included in the first organ and the second organ, a report is generated that the user is not a potential patient for cerebral infarction.
In the system, the cerebral infarction diagnosis model is established in advance, and a relatively accurate prediction means is provided for predicting the potential risk of the cerebral infarction.
In one embodiment, the system further comprises a user information collecting module for collecting user information of the user, wherein the user information comprises gender and age; the monitoring server is further configured to send the user information of the user, the physiological index that does not fall within the preset physiological index, and the detection cycle identifier and the detection result corresponding to the physiological index to the monitoring terminal. The personnel at the monitoring terminal can conveniently acquire the user information, so that the medical measures can be taken for the user in a targeted manner.
In one embodiment, the monitoring server analyzes the potential risk of the cerebral infarction of the user according to the detection result corresponding to each detection period and a preset cerebral infarction diagnosis model, and the method includes:
the monitoring server acquires a matching model matched with the gender and the age of the user from a preset cerebral infarction diagnosis model according to the gender and the age of the user;
and analyzing the potential risk of the cerebral infarction of the user according to the detection result and the matching model corresponding to each detection period.
The system can predict the user according to the information of the user such as gender, age and the like and the corresponding cerebral infarction diagnosis model, fully considers the difference and individuality of different genders and ages in cerebral infarction diagnosis, and improves the prediction accuracy.
In one embodiment, the system may further include:
and the client is in communication connection with the monitoring server and is used for acquiring an analysis result obtained after the monitoring server analyzes the potential risk of the cerebral infarction of the user and displaying the analysis result to the user.
Therefore, the user can obtain the analysis result of the potential risk of the cerebral infarction at any time and know the situation in time.
In an embodiment, the monitoring server is further configured to send the analysis result to the client when the analysis result obtained after the analysis of the potential risk of the cerebral infarction of the user is a preset result. For example, when the analysis result shows that the user is a potential cerebral infarction patient, the analysis result is sent to the client; when the analysis result shows that the user is not a potential cerebral infarction patient, not sending the analysis result to the client; therefore, the information can be selectively sent, the processing load on the monitoring server is reduced, the information interaction between the monitoring server and the client is reduced, and the network resources between the monitoring server and the client are saved.
In one embodiment, the system further comprises:
the user working time acquisition module is used for acquiring the working time of the user in each detection period; for example, the working time of the user in each detection period is obtained from a working time counting server of a unit where the user is located;
and the server is further used for analyzing the potential risk of the cerebral infarction of the user according to the detection result corresponding to each detection period, the working time of the user in each detection period and a preset cerebral infarction diagnosis model. Specifically, for example, when a report that the user is a potential cerebral infarction patient is generated according to the detection result corresponding to each detection period and the preset cerebral infarction diagnosis model, further, the sum of the working time of the user in all the detection periods may be determined, and when the sum is equal to or greater than a preset time, a report that the user is a high risk group of the potential cerebral infarction patients is generated. Thus, a reference standard can be provided for prediction according to the working intensity of the user.
In one embodiment, the system may further include a cerebral infarction detection module;
the cerebral infarction detection module comprises a detection unit of ribonucleic acid LOC 105376505; the detection unit of LOC105376505, used for the expression down-regulation in patients with ischemic cerebral infarction;
the detection unit of LOC105376505 comprises a control chip and a detection device; the detection device is a specific primer of LOC105376505 and is used for detecting ribonucleic acid LOC 105376505;
the detection device of the detection unit of the ribonucleic acid LOC105376505 is prepared by a sequencing technology, a nucleic acid hybridization technology and a nucleic acid amplification technology;
the cerebral infarction detection module is connected with the processing module, and the processing module receives the detection information transmitted by the cerebral infarction detection module and transmits the detection information to the client;
the clock module is connected with the processing module, and when the cerebral infarction detection module transmits data to the processing module, the clock module transmits the data transmission time of the cerebral infarction detection module to the processing module;
and the clock module comprises a positioning device and a local clock device, and the clock module synchronously corrects the local clock device through clock signals in the positioning device.
In one embodiment, the body detection device further comprises a blood routine biochemical detection module;
the blood routine biochemical detection module comprises a blood routine detection unit, a transmission unit, a biochemical detection unit and a control component;
the transmission unit comprises a blood drawing component, the blood drawing component is respectively connected with the conventional blood detection unit and the biochemical detection unit, and the blood drawing component is used for transmitting the blood sample drawn in the conventional blood detection unit to the biochemical detection unit;
the control assembly is connected with the blood routine detection unit, the transmission unit and the biochemical detection unit and is used for controlling the blood routine biochemical detection module;
the transmission unit further comprises a first control switch, a second control switch and a blood discharge assembly, one end of the blood drawing assembly is connected with the conventional blood detection unit through the first control switch, the other end of the blood drawing assembly is connected with the blood discharge assembly through the second control switch, and the blood discharge assembly is connected with the biochemical detection unit; when the first control switch is turned on and the second control switch is turned off, the blood drawing assembly draws the blood sample output by the conventional blood detection unit; when the first control switch is closed and the second control switch is opened, the blood drawing component transmits the drawn blood sample to the biochemical detection unit;
the blood routine detecting unit, the biochemical detecting unit, the control component and the processing module, and the processing module receives the detection information of the blood routine detecting unit and the biochemical detecting unit.
A blood immunoassay module including a blood lysing unit, a first illumination device, a first light receiving device, a first analyzing device, a blood reagent unit, a second illumination device, a second light receiving device, and a second analyzing device;
a blood lysing unit for adding a blood lysing agent to the blood sample;
a first illumination device for illuminating a first blood sample, the first blood sample being a blood sample to which a blood lysing agent is added;
a first light receiving device for receiving the light emitted from the first illuminating device and transmitted through the first blood sample and detecting the intensity of the light received by the first blood sample;
a first analysis device for obtaining the concentration of hemoglobin in the blood sample based on the intensity of light received by the first blood sample;
a blood reagent unit for adding an immunological reagent to the first blood sample;
a second illumination device for illuminating a second blood sample, the second blood sample being the first blood sample to which the immunoreagent is added;
a second light receiving means for receiving light emitted from the second illuminating means and transmitted through the second blood sample and detecting intensity of illumination received by the second blood sample;
a second analysis device for analyzing the substance concentration of the obtained blood sample according to the intensity of the light received by the second blood sample and the hemoglobin concentration of the blood sample obtained by the first analysis device;
the blood immunity detection module is connected with the processing module and is used for transmitting the detection information acquired by the blood immunity detection module to the processing module;
the processing module is used for transmitting the received blood immunity detection information, the blood conventional biochemical detection information and the cerebral infarction detection information to the monitoring server through an encryption algorithm;
and the monitoring server decrypts the transmitted detection information according to the key of the preset encryption algorithm to acquire the detection information.
The beneficial effects of the above technical scheme are that: the first blood sample of gathering is handled and is produced the second blood sample, measures the hemoglobin concentration in the blood sample through to the second blood sample, has reduced and has detected required blood sample volume, has reduced the check-out time, has reduced the cost that detects, has also alleviateed the pain when gathering the blood sample to the patient simultaneously, can be through the accurate hemoglobin concentration who detects in the simple operation and the material concentration of blood sample.
In one embodiment, as shown in fig. 3, the bracelet includes two wristbands and a bracelet body 31 disposed between the two wristbands; of the two wristbands, the first wristband 32 is longer than the second wristband 33.
The first wrist strap 32 has an accommodating space 33 therein, and the accommodating space 33 is communicated with the outside through a hole on the first wrist strap 32; a bendable plate-like body 34, the plate-like body 34 being movably disposed in the accommodating space 33 and being detachable from the wrist band through the hole; a data plug 35 is arranged at one end of the plate-shaped body 34 close to the connecting end of the first wrist strap 32 and the first wrist strap 31, and a data jack 36 matched with the data plug 35 is arranged at one end of the first wrist strap 31 connected with the first wrist strap 32; a plurality of placing grooves 37 are formed in the inner surface of the plate-shaped body 34, a physiological index detecting assembly 38 is placed in each placing groove 37, and each physiological index detecting assembly 38 is connected with the data plug 35 through a data line arranged in the plate-shaped body 34; the plate-like body 34 is also provided with button cells 36, the button cells 36 being connected to each physiological index detecting assembly 38. When the plate-shaped body 34 is placed inside the first wrist strap 32, the data plug 35 is plugged into the data jack 36, and the inner surface of the first wrist strap 32 is provided with an opening matched with the physiological index detecting component 38, so that when the wrist wears the bracelet and the first wrist strap 32 is worn on the wrist, the physiological index detecting component 38 can also be contacted with the skin of the wrist, thereby achieving the purpose of detection.
The first wrist strap 32 is connected to a first elastic strap 39 at an end (free end) away from the main body of the wrist strap, and the first elastic strap 39 is provided with a buckle connector 310. One end (free end) of the second wrist strap 33 far away from the wrist strap body is connected with a second elastic belt 311, and a fastening hole 312 adapted to the fastening head 310 is disposed on the second elastic belt 311.
In the above-described bracelet, the plate-like body 34 can be detached from the bracelet, and when the bioassay function is to be used, the plate-like body 34 is inserted into the first wristband 32, and when the bioassay function is not to be used, the plate-like body 34 is pulled out of the first wristband 32. The plate-shaped body 34 can be conveniently inserted into the data socket 36 of other mobile terminals, so that other mobile terminals can conveniently obtain physiological detection results.
In another embodiment, as shown in fig. 4 and 5, the bracelet main body includes a dial plate on which a display screen can be arranged, a power supply or other modules can be arranged inside the dial plate, and a back cover 41 is arranged at the bottom of the dial plate and is rectangular or square; the conventional back cover 41 is fixed at the bottom end of the dial plate through screws, but the back cover 41 can be opened only by a special screwdriver in the mode, which is inconvenient. The embodiment of the invention improves the rear cover and provides a back stage which is convenient to open and close, wherein the plate-shaped body 34 is made of hard material, such as metal, and is in a semi-annular shape (as shown in fig. 5).
One side of the back cover 41 is rotatably connected to the bottom end frame of the dial, the inner surface of the back cover 41 is further provided with a micro motor 42, a driving shaft 43 of the micro motor 42 penetrates through the other side of the back cover 41 (which belongs to the adjacent side with the one side of the back cover 41), the driving shaft 43 is perpendicular to the other side, a gear 44 penetrates through the driving shaft 43, and the gear 44 can be driven by the driving shaft 43 to rotate; the micro motor 42 is used for driving the driving shaft 43 to rotate; the micro-motor 42 is connected to a power supply within the dial. A processor 45 is also arranged in the dial, a key 46 is also arranged on the dial, and when the key 46 is pressed once, the processor 45 controls the micro motor 42 to drive the driving shaft 43 to rotate; when the button 46 is pressed next time, the processor 45 controls the micro motor 42 to drive the driving shaft 43 to stop rotating. The rotating drive shaft 43 rotates the gear 44.
The bottom end of the dial is provided with a groove 51 with the shape matched with that of the rear cover 41 of the associated gear 44; wherein, the lower end of the part of the groove 51 which is matched with the gear 44 is provided with a jack 52, and the jack 52 is matched with the shape of the data plug 35; in the use state, the back cover 41 with the gear 44 is positioned in the groove 51, so as to achieve the effect of closing the dial. The jack 52 may be a data jack adapted to the shape of the data plug 35, and in this case, it functions not only as a fixed rail but also as a spare jack for the data jack 36 by guiding data in the plate-like body into the bracelet body.
One circumferential edge of the inner surface of the plate-like body 34 is provided with a guide rail 53 (not shown) which is engaged with the gear 44;
when it is desired to open the rear cover 41, the semi-annular plate-like body is pulled out from the first wrist band 32, the data plug 35 is inserted into the insertion hole 52, and the guide rail 53 of the plate-like body faces the gear 44. When the user presses the button 46, the processor 45 controls the micro-motor 42 to drive the gear 44 to start rolling along the guide rail 53, and the guide rail 53 drives the gear 44 to continuously advance along the guide rail 53, so as to open the rear cover 41. After opening, the plate-like body 34 is pulled out from the insertion hole 52, and the rear cover 41 is manually pushed into the recess 51.
In the structure, the plate-shaped body additionally serves as the guide rail without additionally configuring a special guide rail, so that the whole structure of the bracelet is simplified, and the bracelet is convenient and quick to use.
In one embodiment, there may be a plurality of monitoring terminals, and there may also be a plurality of backend servers, and when the monitoring terminal is an application program, each backend server is responsible for information transmission with the monitoring terminal registered in the backend server.
In another embodiment, the monitoring terminal that is not registered with the background server may also request the preset information from the background server, at this time, the system may further include an allocation server, at this time:
the method comprises the steps that a distribution server obtains an information obtaining request transmitted by a monitoring terminal, wherein the information obtaining request comprises a network address range of a preset geographic area and the current geographic position of the monitoring terminal;
the distribution server searches for at least one background server with a network address located in the network address range of the preset geographic area; acquiring at least one target background server in an accessible state from the at least one background server, and distributing a server identifier for each target background server; transmitting the server identification of at least one target background server to the monitoring terminal for selection by a user of the monitoring terminal; the monitoring terminal receives a server identification selected by a user, the selected server identification is sent to a distribution server, the distribution server searches background server information matched with the server identification in a prestored information base according to the selected server identification, a network address range corresponding to each geographical area and all background server information belonging to each network address range are stored in the information base, and the background server information comprises the network address of the background server, the server identification, state information and geographical area information of the monitoring terminal which is allowed to access the background server; judging whether the current geographic position of the monitoring terminal is located in a geographic area of the monitoring terminal which allows the access of the matched background server, and if not, returning a notification of forbidding the access to the monitoring terminal; if so, acquiring the network address of the matched background server and sending the network address to the monitoring terminal, and establishing the connection between the matched background server and the monitoring terminal.
After the connection between the matched background server and the monitoring terminal is established, information transmission can be realized between the matched background server and the monitoring terminal. The technical scheme can facilitate personnel to obtain the background server which is required to be accessed and is not registered through the monitoring terminal, and access is performed under the permission of the background server, so that the information security is ensured.
The establishing of the connection between the matched background server (hereinafter referred to as background server) and the monitoring terminal may be implemented as:
when the monitoring terminal registers to the transfer server, the transfer server and the monitoring terminal perform authentication and key agreement, and respectively generate authentication information for establishing a secure channel for the background server and the monitoring terminal; after the authentication information is generated, the transit server and the monitoring terminal respectively store the generated authentication information; the generation of the authentication information can be realized by adopting the prior art, and is not described in detail herein. The transfer server positions a management server of the monitoring terminal; the method of the transit server locating the management server may be obtained based on address information of the management server provided by the monitoring terminal in the transit server. The transfer server sends the generated authentication information and the identification of the monitoring terminal to a management server through a secure channel; when the monitoring terminal sends a data acquisition request to the background server within a preset time, the background server initiates inquiry to the management server to acquire the state of the monitoring terminal; if the monitoring terminal is in a login state, the management server returns an identifier of the monitoring terminal and authentication information required by the monitoring terminal and the background server to establish a secure channel besides returning the state of the monitoring terminal to the background server;
if the monitoring terminal is not logged in, the background server sends a first request message for requesting the monitoring terminal to log in to the management server, wherein the first request message comprises an identifier of the monitoring terminal and an identifier of the background server;
the management server sends a first request message to the transfer server through the secure channel;
the transfer server sends a first request message to the mobile equipment where the monitoring terminal is located;
when the mobile equipment receives the first request message, starting the monitoring terminal, and sending a second request message to the monitoring terminal, wherein the second request message comprises the identifier of the background server;
after receiving the second request message, the monitoring terminal, according to the identifier of the background server in the second request message,
judging whether the identification of the background server of the receiving party corresponding to the data acquisition request sent by the monitoring terminal is consistent with the identification of the background server in the second request message; when the network channels are consistent, a network channel from the monitoring terminal to the background server is established;
the monitoring terminal and the background server perform mutual authentication of the monitoring terminal and the background server based on the authentication information, and after the authentication is passed, end-to-end data security transmission connection between the monitoring terminal and the background server is formed.
The method for establishing the data security transmission connection can improve the security of information transmission between the monitoring terminal and the background server.
After the data security transmission connection is established, the background server encrypts preset information according to network transmission configuration information to obtain encrypted data, wherein the network transmission configuration information is used for carrying out encryption classification on the network data and configuring a security strategy;
the background server sends the encrypted data to the monitoring terminal through the data security transmission connection; and the monitoring terminal decrypts the encrypted data after receiving the encrypted data to obtain preset information. The transmission safety of the preset information is improved.
It will be apparent to those skilled in the art that various changes and modifications may be made in the present invention without departing from the spirit and scope of the invention. Thus, if such modifications and variations of the present invention fall within the scope of the claims of the present invention and their equivalents, the present invention is also intended to include such modifications and variations.
Claims (10)
1. A body detection system for cerebral infarction detection, comprising:
the body detection device is used for detecting the physiological index of the user according to a preset detection period to obtain a detection result corresponding to each detection period;
the monitoring server is used for analyzing whether each physiological index in the detection result corresponding to each detection period falls into a preset physiological index or not; when a physiological index which does not fall into a preset physiological index exists, sending the physiological index which does not fall into the preset physiological index, a detection cycle identifier corresponding to the physiological index and a detection result to a monitoring terminal;
the memo application is used for the user to use and is used for recording the memo schedule of the user in each detection period and sending the memo schedule corresponding to each detection period to the monitoring server;
the monitoring server is also used for determining whether the same memo schedule with the repetition times exceeding the preset times exists according to the memo schedule corresponding to each detection period; if yes, the same memo schedule is sent to the monitoring terminal;
the monitoring server is also used for analyzing the importance degree of the same memo schedule, wherein the memo application marks the importance degree corresponding to each memo schedule according to the setting of a user and sends the same memo schedule and the importance degree to the monitoring server, the monitoring server scores the same memo schedule according to the importance degree of the same memo schedule and the overrun times that the same memo schedule exceeds the preset times, and the scoring formula is as follows: q = Z N, wherein Q is the final score of the same memo schedule, Z is the weight corresponding to the importance degree of the same memo schedule, the higher the importance degree is, the larger the weight is, the specific weight value is set by self, N is the number of times of overrun, and the monitoring server sends the score corresponding to the same memo schedule, the same memo schedule and the number of times of overrun to the monitoring terminal.
2. The system of claim 1, wherein said body-testing device further comprises a blood routine biochemical test module;
the blood routine biochemical detection module comprises a blood routine detection unit, a transmission unit, a biochemical detection unit and a control component;
the transmission unit comprises a blood drawing component, the blood drawing component is respectively connected with the conventional blood detection unit and the biochemical detection unit, and the blood drawing component is used for transmitting the blood sample drawn in the conventional blood detection unit to the biochemical detection unit;
the control assembly is connected with the blood routine detection unit, the transmission unit and the biochemical detection unit and is used for controlling the blood routine biochemical detection module;
the transmission unit further comprises a first control switch, a second control switch and a blood discharge assembly, one end of the blood drawing assembly is connected with the conventional blood detection unit through the first control switch, the other end of the blood drawing assembly is connected with the blood discharge assembly through the second control switch, and the blood discharge assembly is connected with the biochemical detection unit;
when the first control switch is turned on and the second control switch is turned off, the blood drawing assembly draws the blood sample output by the conventional blood detection unit; when the first control switch is closed and the second control switch is opened, the blood drawing component transmits the drawn blood sample to the biochemical detection unit;
the blood routine detection unit, the biochemical detection unit, the control component and the processing module, wherein the processing module receives detection information of the blood routine detection unit and the biochemical detection unit;
a blood immunoassay module including a blood lysing unit, a first illumination device, a first light receiving device, a first analyzing device, a blood reagent unit, a second illumination device, a second light receiving device, and a second analyzing device;
a blood lysing unit for adding a blood lysing agent to the blood sample;
a first illumination device for illuminating a first blood sample, the first blood sample being a blood sample to which a blood lysing agent is added;
a first light receiving device for receiving the light emitted from the first illuminating device and transmitted through the first blood sample and detecting the intensity of the light received by the first blood sample;
a first analysis device for obtaining the concentration of hemoglobin in the blood sample based on the intensity of light received by the first blood sample;
a blood reagent unit for adding an immunological reagent to the first blood sample;
a second illumination device for illuminating a second blood sample, the second blood sample being the first blood sample to which the immunoreagent is added;
a second light receiving means for receiving light emitted from the second illuminating means and transmitted through the second blood sample and detecting intensity of illumination received by the second blood sample;
a second analysis device for analyzing the substance concentration of the obtained blood sample according to the intensity of the light received by the second blood sample and the hemoglobin concentration of the blood sample obtained by the first analysis device;
the blood immunity detection module is connected with the processing module and is used for transmitting the detection information acquired by the blood immunity detection module to the processing module;
the processing module is used for transmitting the received blood immunity detection information, the blood conventional biochemical detection information and the cerebral infarction detection information to the monitoring server through an encryption algorithm;
and the monitoring server decrypts the transmitted detection information according to the key of the preset encryption algorithm to acquire the detection information.
3. Body detection system as claimed in claim 1 or 2,
and the monitoring server is also used for analyzing the potential risk of the cerebral infarction of the user according to the detection result corresponding to each detection period and a preset cerebral infarction diagnosis model.
4. The system of claim 1 or 2,
the body detection device comprises a bracelet, wherein a physiological index detection assembly is arranged on the bracelet, and the physiological index detection assembly comprises any one or more of a heart rate detection assembly, a pulse detection assembly, a blood oxygen value detection assembly and a blood pressure detection assembly.
5. The system of claim 4,
the bracelet comprises two wristbands and a bracelet main body 31 arranged between the two wristbands; the first bracelet 32 of the two bracelets is longer than the second bracelet 33;
the first wrist strap 32 has an accommodating space 33 therein, and the accommodating space 33 is communicated with the outside through a hole on the first wrist strap 32; a bendable plate-like body 34, the plate-like body 34 being movably disposed in the accommodating space 33 and being detachable from the wrist band through the hole; a data plug 35 is arranged at one end of the plate-shaped body 34 close to the connecting end of the first wrist strap 32 and the first wrist strap 31, and a data jack 36 matched with the data plug 35 is arranged at one end of the first wrist strap 31 connected with the first wrist strap 32; a plurality of placing grooves 37 are formed in the inner surface of the plate-shaped body 34, a physiological index detecting assembly 38 is placed in each placing groove 37, and each physiological index detecting assembly 38 is connected with the data plug 35 through a data line arranged in the plate-shaped body 34; the plate-shaped body 34 is also provided with a button battery 36, and the button battery 36 is connected with each physiological index detection assembly 38; when the plate-shaped body 34 is placed in the first wrist strap 32, the data plug 35 is plugged into the data jack 36, and the inner surface of the first wrist strap 32 is provided with an opening matched with the physiological index detection component 38, so that when the wrist wears a bracelet, and the first wrist strap 32 is worn on the wrist, the physiological index detection component 38 can also be contacted with the skin of the wrist, thereby achieving the purpose of detection;
one end of the first wrist strap 32, which is far away from the bracelet body, is connected with a first elastic belt 39, a buckle connector 310 is arranged on the first elastic belt 39, one end of the second wrist strap 33, which is far away from the bracelet body, is connected with a second elastic belt 311, and a buckle hole 312 adapted to the buckle connector 310 is arranged on the second elastic belt 311.
6. The system of claim 3,
analyzing the potential risk of the cerebral infarction of the user according to the detection result corresponding to each detection period and a preset cerebral infarction diagnosis model, wherein the analysis comprises the following steps:
step 1: acquiring detection results corresponding to N1 continuous detection periods from the body detection device to obtain N1 detection results; determining whether the N1 is equal to or greater than N; if yes, continuing to step 2; otherwise, ending the flow;
step 2: determining the number of a first group of detection results of which the blood pressure value is greater than a preset blood pressure value from the N1 detection results; continuing to step 3 when the number of the first set of detection results is equal to or greater than N2; when the number of the first group of detection results is less than N2, deleting the N1 detection results, and reusing the body detection device for detection;
and step 3: when the number of the first group of detection results is equal to or larger than N2, judging whether the detection period corresponding to each detection result in the first group of detection results is adjacent; when not adjacent, returning to the step 1; when adjacent, continuing to step 4;
and 4, step 4: when the detection periods corresponding to each detection result in the first group of detection results are adjacent, determining the number of the second group of detection results when the organ of the user is in the sub-health state according to the N1 detection results; judging whether the number of the second group of detection results is equal to or larger than N3; when the number of the second group of detection results is equal to or greater than N3, recording the first organ in the sub-health state, and continuing to the step 5;
and 5: determining a second organ with a blood oxygen value equal to or less than a preset blood oxygen value from the N1 test results; judging the number of detection results that the blood oxygen value of the second organ is equal to or less than a preset blood oxygen value; when the number is equal to or greater than N4, recording a second organ, and continuing with step 6; when the number is less than N4 and greater than 1, returning to the step 5; when the number is equal to 0, ending the flow;
step 6: and taking the first organ, the second organ, the first group of detection results and the second group of detection results as a basis for judging whether the user has a potential cerebral infarction risk, and analyzing the potential cerebral infarction risk of the user by combining a preset cerebral infarction diagnosis model to generate an analysis report.
7. The system of claim 6,
the preset cerebral infarction diagnosis model at least comprises a value range of physiological indexes of preset organs of a cerebral infarction potential patient;
the step 6 includes:
judging whether the first organ and the second organ contain the preset organ or not;
when the first organ and the second organ contain the preset organ, judging whether the physiological index corresponding to the first organ in the first group of detection results is located in a value range of the physiological index corresponding to the first organ and judging whether the physiological index corresponding to the second organ in the second group of detection results is located in a value range of the physiological index corresponding to the second organ; when the two judgment results are yes, generating a report that the user is a potential cerebral infarction patient; when at least one of the two judgment results is negative, generating a report that the user is not a potential cerebral infarction patient;
generating a report that the user is not a potential patient for cerebral infarction when the predetermined organ is not included in the first and second organs.
8. The system of claim 1,
the system also comprises a user information acquisition module for acquiring user information of the user, wherein the user information comprises gender and age;
the monitoring server is further configured to send the user information of the user, the physiological index that does not fall within the preset physiological index, and the detection cycle identifier and the detection result corresponding to the physiological index to the monitoring terminal.
9. The system of claim 8,
the monitoring server analyzes the potential risk of the cerebral infarction of the user according to the detection result corresponding to each detection period and a preset cerebral infarction diagnosis model, and the method comprises the following steps:
the monitoring server acquires a matching model matched with the gender and the age of the user from a preset cerebral infarction diagnosis model according to the gender and the age of the user;
and analyzing the potential risk of the cerebral infarction of the user according to the detection result corresponding to each detection period and the matching model.
10. The system of claim 1, further comprising:
the client is in communication connection with the monitoring server and used for acquiring an analysis result obtained after the monitoring server analyzes the potential risk of the cerebral infarction of the user and displaying the analysis result to the user;
and the monitoring server is further used for sending the analysis result to the client when the analysis result obtained after the analysis of the potential risk of the cerebral infarction of the user is a preset result.
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