WO2018223541A1

WO2018223541A1 - Barcode scanning-based clinical test report review system and method

Info

Publication number: WO2018223541A1
Application number: PCT/CN2017/100171
Authority: WO
Inventors: 张贯京; 葛新科; 王海荣; 魏琼东; 高伟明; 周亮
Original assignee: 深圳市前海安测信息技术有限公司
Priority date: 2017-06-10
Filing date: 2017-09-01
Publication date: 2018-12-13
Also published as: CN107292096A

Abstract

A barcode scanning-based clinical test report review system (20) and method. The method comprises: generating, according to medical testing instruction information, testing barcodes, and controlling a barcode device (7) to print the same; when each of the testing barcodes corresponds to one start state field information item and one end state field information item, receiving test result data of all testing apparatuses (4), generating a test report, and associating the same with an electronic signature of review personnel; sending the test report to a doctor terminal (6) of the review personnel for review; and when the test report is reviewed by the review personnel, locking the test report in a read-only mode, and generating an official test report. The present invention enables monitoring of a testing process by means of barcode, thus improving test efficiency, and reducing medical malpractice resulting from clinical test errors. In addition, a test report is locked to improve information security thereof.

Description

Clinical inspection report review system and method based on barcode scanning

[0001] The present invention relates to the field of medical information, and in particular, to a clinical test report review system and method based on barcode scanning.

Background technique

[0002] As a medical discipline, clinical laboratory plays an important role in the diagnosis and examination of clinical diseases. It is an important task and responsibility of the hospital laboratory to apply modern laboratory techniques and accurately provide a reliable basis for clinical diagnosis. Clinical examinations generally include multiple inspection subjects such as clinical examination, biochemistry, immunity, microbes, and AIDS testing points. The clinical laboratory work provides an accurate and scientific basis for clinical diagnosis of diseases, tracking of curative effects and estimation of prognosis for various diseases from biochemistry, hematology, cytology, immunology, etc.; from pathogens to clinical drug sensitivity tests and bacterial resistance Drug monitoring provides clinical use of rational use of antibiotics.

[0003] With the continuous improvement of the automation of inspection equipment, the rapid development of inspection methods and methods, the increasing living standards of the same people, and the gradual emphasis on health, the work intensity and workload of the hospital inspection department are getting bigger and bigger. In the existing clinical testing system, the detection process cannot be transparently monitored, and the user can't check the progress, which not only reduces the detection efficiency, but also directly affects the quality of service to the patient, and may even cause a medical accident.

[0004] Further, the existing detection report does not lock the content of the detection result information in the detection report, so that any person who views the detection report can modify the detection report, thereby reducing the information security of the detection report, and Can cause a medical accident.

technical problem

[0005] The main object of the present invention is to provide a clinical inspection report review system and method based on barcode scanning, which aims to solve the technical problem that the existing clinical inspection system cannot realize the full process transparent monitoring and the detection report cannot be locked.

Problem solution

Technical solution

[0006] In order to achieve the above object, the present invention provides a clinical inspection report review system based on barcode scanning. Running in the data center, the data center is connected to the user terminal, the doctor terminal, the barcode machine and the plurality of detecting devices through the network, and the system comprises:

[0007] a generating module, configured to generate a detection barcode according to the detection medical order information and control the barcode printer to print the detection barcode; [0008] a sending module, configured to: when the liquid specimen in the specimen tube does not belong to the detection device, send a specimen tube detection Sending information to the detecting device to inform the inspector of the specimen tube corresponding to the detecting device, and notifying the detecting personnel to scan the corresponding specimen tube;

[0009] a generating module, configured to generate an initial status bar information and send the information to the user terminal;

[0010] the sending module is configured to: when the detecting device completes the detection of the liquid sample in the specimen tube and scans the detected barcode again, generates an end status bar information and sends the information to the user terminal;

[0011] an association module, configured to: when each detection barcode has a corresponding initial status bar information and an end status bar information, obtain detection result data of all detection devices, generate a detection report, and report and review the detection report Electronic signature of personnel;

[0012] a sending module, configured to send the test report to the doctor terminal of the auditor for review; and

[0013] The locking module is configured to: when the auditor audits the test report, perform read-only locking on the test report, and generate a formal test report.

[0014] Preferably, the detection barcode includes personal information of the user, doctor information, detection item information, and detection device information.

[0015] Preferably, if the detecting device information in the detecting bar code is consistent with the attribute information of the detecting device, determining that the liquid sample in the sample tube belongs to the detecting device, otherwise, if detecting the device information in the detecting bar code and the detecting device If the attribute device information is inconsistent, it is determined that the liquid sample in the sample tube does not belong to the detection device.

[0016] Preferably, the association module receives the detection result data of all the detection devices and puts them into the detection report template in an XML format to complete the generation of the detection report.

[0017] Preferably, the locking module performs read-only locking on the detection result data as follows: The label name corresponding to the detection result data in the detection report template of the XML format is converted to complete the locking of the detection result data.

[0018] On the other hand, a clinical inspection report review method based on barcode scanning is applied to a data center, and the data center is connected to a user terminal, a doctor terminal, a barcode machine, and a plurality of detection devices through a network, Methods include:

[0019] generating a detection barcode according to the detection medical order information and controlling the barcode printer to print the detection barcode;

[0020] when the liquid sample in the specimen tube does not belong to the detecting device detecting flaw, sending the specimen tube detecting information to the detecting device to inform the detecting personnel of the specimen tube corresponding to the detecting device, and notifying the detecting personnel to scan the corresponding specimen tube ;

[0021] generating an initial status bar information and transmitting the information to the user terminal;

[0022] when the detecting device completes the detection of the liquid sample in the specimen tube and scans the detected barcode again, the end status column information is generated and transmitted to the user terminal;

[0023] when each detection bar code has a corresponding initial status bar information and an end status bar information, obtaining detection result data of all detecting devices and generating a detection report, and associating the detection report with the electronic signature of the auditor ;

[0024] sending the test report to the medical terminal of the auditor for review; and

[0025] When the auditor audits the test report, the test report is read-only and a formal test report is generated.

[0026] Preferably, the detection barcode includes personal information of the user, doctor information, detection item information, and detection device information.

[0027] Preferably, if the detecting device information in the detecting bar code is consistent with the attribute information of the detecting device, determining that the liquid sample in the sample tube belongs to the detecting device, otherwise, if detecting the device information in the detecting bar code and the detecting device If the attribute device information is inconsistent, it is determined that the liquid sample in the sample tube does not belong to the detection device.

[0028] Preferably, the detection report is generated in the following manner: The detection result data of all the detection devices is received and placed in a detection report template in an XML format to complete the generation of the detection report.

[0029] Preferably, the locking module performs read-only locking on the detection result data as follows: The label name corresponding to the detection result data in the detection report template of the XML format is converted to complete the locking of the detection result data.

Advantageous effects of the invention

Beneficial effect

[0030] The present invention adopts the above technical solution, and brings the technical effects as follows: The present invention is based on the barcode scanning The bed inspection report review system and method, using barcode method to detect the whole detection process, and notify the user, avoiding human error in the detection process, ensuring that the inspection process is transparent and controllable and the inspection result is correct, improving the detection efficiency and It can effectively reduce the medical accidents caused by mistakes in clinical tests, and can lock the test reports and improve the information security of test reports.

Brief description of the drawing

DRAWINGS

1 is a schematic diagram of an application environment of a clinical test report review system based on barcode scanning according to the present invention.

2 is a schematic block diagram of a preferred embodiment of a clinical examination report review system based on barcode scanning of the present invention.

3 is a flow chart of a preferred embodiment of a clinical test report review method based on barcode scanning according to the present invention.

[0034] The implementation, functional features, and advantages of the present invention will be further described with reference to the accompanying drawings.

BEST MODE FOR CARRYING OUT THE INVENTION

The specific embodiments, structures, features and functions of the present invention are described in detail below with reference to the accompanying drawings and preferred embodiments. It is understood that the specific embodiments described herein are merely illustrative of the invention and are not intended to limit the invention.

[0036] Referring to FIG. 1, FIG. 1 is a schematic diagram of an application environment of a clinical inspection report review system based on barcode scanning according to the present invention.

[0037] The bar code scanning based clinical test report review system 20 of the present invention operates in the data center 2. The data center 2 is connected to the detecting device 4 (which may be one or a plurality of detecting devices 4), the user terminal 5, the doctor terminal 6 and the barcode machine 7 via the network 3.

[0038] The network 3 may be a wired communication network or a wireless communication network. The network 3 is preferably a wireless communication network including, but not limited to, a GSM network, a GPRS network, a CDMA network, a TD-SCDMA network, a WiMAX network, a TD-LTE network, an FDD-LTE network, and the like.

[0039] The detecting device 4 is a detecting device capable of detecting body composition by a liquid sample having a network connection function (for example, including a WIFI module, a network interface, etc.), for example, an immunoanalyzer (ie, for detecting a tumor marker) , anemia, thyroid, pregnancy screening, and other medical equipment), blood analyzer ( For example, medical instruments for detecting human red blood cells and white blood cells, urine detectors (ie, automated instruments for measuring certain chemical components in urine, such as urine protein, urine glucose, urine pH, urine ketone bodies, etc., by urine) Urinary bilirubin, urinary biliary tract, urinary occult blood, nitrite, urinary leukocyte, urine specific gravity, vitamin C and/or turbidity, etc., biochemical analyzer (ie, according to the photoelectric colorimetric principle to measure a specific chemistry in body fluids) Ingredients for medical devices that can be used to detect human alanine aminotransferase (ALT/GPT), aspartate aminotransferase (AST/GOT), alkaline phosphatase (ALP), total bilirubin (T.BIL), direct bilirubin

(D.BIL), total protein (TP), albumin (ALB), urea nitrogen (BUN), creatinine (Cre), carbon dioxide binding (C02), uric acid (UA), total cholesterol (CHO), triglyceride (TG), high-density lipoprotein cholesterol (HDL-C), low-density lipoprotein cholesterol (LDL-C), glucose (GLU), creatine kinase (CK), creatine kinase isoenzyme (CK-MB), Lactate dehydrogenase (L DH), a-hydroxybutyrate dehydrogenase (a-HBDH), glutamyltranspeptidase (r-GT), calcium (Ca), phosphorus (P), magnesium (Mg), Potassium (K), sodium (Na), chlorine (CL) and other ingredients). It should be noted that, in the present embodiment, the data center 2 is connected to a plurality of different types of detecting devices 4.

[0040] The user terminal 5 may be, but not limited to, any other suitable portable electronic device such as a smart phone, a tablet computer, a personal digital assistant (PDA), a personal computer, and the like. It should be noted that the user can view the detection progress and/or the detection result through the user terminal 5.

[0041] The doctor terminal 6 may be, but not limited to, any other suitable electronic device such as a smartphone, a tablet, a personal digital assistant (PDA), a personal computer, or the like. It should be noted that the doctor can stand up to the medical examination through the doctor terminal 6 (for example, detecting urine, detecting hemoglobin, etc.). It should be noted that since the doctor is generally located in a fixed position, the medical terminal 6 is a personal computer.

[0042] Further, the data center 2 is configured to generate a detection barcode according to a doctor's prescription for detecting a doctor, the detection barcode includes personal information of the user (for example, information such as age, gender, etc.), and doctor information (for example, a doctor) Name, doctor gender, doctor's department and other information), test item information (for example, test items) and test equipment information (for example, equipment model, equipment name, equipment department, equipment location, etc.). In this embodiment, the detection bar code is a two-dimensional bar code (e.g., a linear stacked two-dimensional code, a matrix two-dimensional code, and/or a color bar code) capable of accommodating a large amount of information.

[0043] The barcode machine 7 is configured to receive a detection barcode from the data center 2 and print out a paper barcode. Among them, playing The printed paper bar is attached to the outer surface of the specimen tube (i.e., the medical tube containing the liquid sample taken from the human body), and the detecting device 4 performs scanning. The detecting device 4 further includes a display device (for example, a display) and a scanner (for example, an infrared scanner), wherein the scanner is configured to scan the detected barcode to detect the barcode. The information is verified, and the display device is configured to display the verification result (for example, whether the specimen tube is detected by the detecting device 4) to facilitate inspection by the inspection personnel. It should be noted that, in order to reduce errors, the specimen tubes are distinguished by color (for example, the lids of the specimen tubes are distinguished by different colors), and the borders of the detection barcodes are also color-coded (generally, paper-based The detection barcode includes an information area and a white border area. In this embodiment, the white border area is changed to a color corresponding to the specimen tube, for example, the red specimen tube corresponds to the detection barcode of the red border. Avoid error when posting barcodes on each specimen tube

Further, the data center 2 is connected to the detecting device 4 (which may be one or a plurality of detecting devices 4), the user terminal 5, the doctor terminal 6, and the barcode machine 7 via the network 3. It should be noted that the data center 2 is a server in the cloud platform or the cloud platform, and the data transmission capability and data storage capability of the data center 2 can better manage and/or assist with the data center. The connected detection device 4, the user terminal 5, the doctor terminal 6 and the barcode machine 7 are beneficial to the user and the user to understand the results of the clinical examination, and the doctors and the inspectors are also required to monitor the detection process to avoid omission.

[0045] Further, the data center 2 further includes an electronic signature of the auditor, and the electronic signature is dynamically generated by the detection report cloud platform 1 according to the information of the auditor (for example, name, department, position, etc.) generate. The electronic signature may be, but is not limited to, a CA electronic signature certificate. The electronic signature may be encrypted, but is not limited to, asymmetric key encryption, computer password, biological handwriting recognition, fingerprint recognition, and iris iris perspective discrimination, face recognition, and the like. At present, the most mature electronic signature technology is the "digital signature", which is an electronic signature made by the "asymmetric" cryptography of public keys and keys. The technology for generating an electronic signature is a prior art and will not be described here.

[0046] Referring to FIG. 2, it is a block diagram of a preferred embodiment of a clinical test report review system based on bar code scanning of the present invention. In this embodiment, the barcode scan based clinical test report review system 20 is applied to the data center 2. The data center 2 includes, but is not limited to, a bar code scanning based clinical test report review system 20, a storage unit 22, a processing unit 24, and a communication unit 26. [0047] The storage unit 22 may be a read only storage unit ROM, an electrically erasable storage unit EEPRO M, a flash storage unit FLASH or a solid hard disk.

[0048] The processing unit 24 may be a central processing unit (CPU), a microcontroller (MCU), a data processing chip, or an information processing unit having a data processing function.

[0049] The communication unit 26 is a wireless communication interface with remote wireless communication functions, for example, supports communication technologies such as GSM, GPRS, WCDMA, CDMA, TD-SCDMA, WiMAX, TD-LTE, FDD-LT E, and the like. Communication interface.

[0050] The bar code scanning-based clinical test report review system 20 includes, but is not limited to, a generating module 20 0, a determining module 210, a sending module 220, an associating module 230, and a locking module 240. The module referred to in the present invention is A series of computer program instructions that can be executed by the processing unit 24 of the data center 2 and that are capable of performing a fixed function are stored in the storage unit 22 of the data center 2.

[0051] The generating module 200 is configured to generate a detection barcode according to the detection medical order information and control the barcode printer 5 to print the detection barcode. Specifically, when the user sees a doctor at the doctor, the doctor inputs the medical examination information for the user through the doctor terminal 6 (for example, detecting urine, detecting hemoglobin, etc.), and transmitting the medical information to the data center 2, The generation module 200 generates a detection barcode based on the detected medical order information and prints it by the control barcode machine 7. In this embodiment, the generating module 200 calls a barcode encoder (for example, a two-dimensional code encoder) installed in the data center 2 to generate a detection barcode. It should be noted that the test barcode after printing is attached to the outer surface of the specimen tube by a hospital staff (for example, a nurse), and then the hospital's laboratory collects the user's liquid specimen (blood, body fluid, sputum, and/or urine, etc.). Other liquids produced by the human body) into the specimen tube.

[0052] The determining module 210 is configured to: when the detecting device 4 scans the detecting bar code on the specimen tube to be detected, determine whether the liquid specimen in the specimen tube belongs to the detecting device 4 to detect. Specifically, the sample tube to be detected is provided with a user liquid sample, and the scanner of the detecting device 4 scans the detection barcode on the specimen tube, and the scanned barcode and the attribute information of the detecting device 4 (detection device) The information, for example, the device model, the device name, the device belonging to the device, the device location, and the like are transmitted back to the data center 2. The determining module 210 parses the detected device information in the returned detection barcode and performs comparison, if the barcode is detected. If the detection device information is consistent with the attribute information returned by the detection device 4, it indicates that the liquid sample in the sample tube belongs to the detection device 4, otherwise, if the detection device information in the detection barcode is returned by the detection device 4 If the attribute information is inconsistent, it indicates that the liquid sample in the specimen tube does not belong to the detection device 4 for detection.

[0053] The sending module 220 is configured to send the specimen tube detection information (for example, the number, color, and the like of the specimen tube to be detected by the detecting device 4) when the liquid specimen in the specimen tube does not belong to the detecting device 4 detecting the flaw. The detecting device 4 is notified to the inspector of the specimen tube corresponding to the detecting device 4, and the detecting personnel is notified to scan the corresponding specimen tube.

[0054] The generating module 200 is configured to generate an initial status bar information and send it to the user terminal 5. In this embodiment, the start status bar information is used to indicate that liquid sample detection within the sample tube has begun.

[0055] The sending module 220 is configured to generate an end status bar information and send the information to the user terminal 5 when the detecting device 4 completes the detection of the liquid sample in the specimen tube and scans the detected barcode again. In this embodiment, the end status bar information is used to indicate that the liquid sample detection in the sample tube has ended.

[0056] The determining module 210 is further configured to determine whether each detected barcode has a corresponding initial status bar information and an end status bar information. If the detection bar code does not have a corresponding initial status bar information and an end status bar information, it indicates that the detection item corresponding to the detection bar code has not been completed yet. If each test bar code has a corresponding start status bar information and an end status bar information, it indicates that all test items have been completed in the doctor's test order.

[0057] The association module 230 is configured to acquire detection result data of all the detection devices 4 and generate a detection report, and associate the detection report with an electronic signature of the auditor. Specifically, the association module 230 receives the detection result data of all the detecting devices 4 and puts them into the detection report template in the XML format, thereby generating a detection report.

[0058] The sending module 220 is configured to send a test report to the doctor terminal 6 of the auditor for review. In the present embodiment, the reviewer generally refers to a senior doctor (e.g., a deputy chief physician or chief physician). It should be noted that the doctor terminal 6 of the auditor obtains the electronic signature of the auditor from the data center 2, and checks the sent test report by the obtained electronic signature verification, and then the test report and the auditor's Electronic signature association.

[0059] The determining module 210 is further configured to determine whether the detection report is reviewed. Specifically, the determining module 210 sends the test report to the doctor terminal 6 of the auditor and pops up a confirmation dialog box. When the auditor clicks the confirmation button of the confirmation dialog box, it indicates that the auditor has reviewed the test report. [0060] The locking module 240 is configured to perform read-only locking on the detection report and generate a formal detection report. Specifically, since the detection report is in an XML format, and the XML format includes various tags, the read-only locking of the detection result data can be completed by converting the tags of the corresponding regions in the XML. The manner in which the locking module 240 performs read-only locking on the detection report is as follows: The label name of the detection report template in the XML format is converted to complete the locking of the detection report. After the name conversion, the data in the label cannot be modified, edited, etc. After the conversion, due to the change of the labels of each level, even if the test report of Zhang San is modified, the corresponding data insertion position cannot be found in the detection report after the read-only lock, and the test report of Zhang San cannot be modified. . In addition, the formal test report further includes a two-dimensional code for the patient to scan through the two-dimensional code. The basic information of the patient is included in the two-dimensional code, and the generation method of the two-dimensional code is prior art, and details are not described herein.

Referring to FIG. 3, there is shown a flow chart of a preferred embodiment of the clinical test report review method based on bar code scanning of the present invention. In this embodiment, the bar code scanning-based clinical test report review method is applied to the data center 2, and the method includes the following steps:

[0062] Step S10: The generating module 200 generates a detection barcode according to the detection medical order information and prints it by the control barcode machine 5. Specifically, when the user sees a doctor at the doctor, the doctor inputs the medical examination information for the user through the doctor terminal 6 (for example, detecting urine, detecting hemoglobin, etc.), and transmitting the medical information to the data center 2, The generation module 200 generates a detection barcode based on the detected medical order information and prints it by the control barcode machine 7. In this embodiment, the generating module 200 calls a barcode encoder (for example, a two-dimensional code encoder) installed in the data center 2 to generate a detection barcode. It should be noted that the test barcode after printing is attached to the outer surface of the specimen tube by a hospital staff (for example, a nurse), and then the hospital's laboratory collects the user's liquid specimen (blood, body fluid, sputum, and/or urine, etc.). Other liquids produced by the human body) into the specimen tube.

[0063] Step S11: When the detecting device 4 scans the detecting bar code on the specimen tube to be detected, the determining module 210 determines whether the liquid specimen in the specimen tube belongs to the detecting device 4 for detection. Specifically, the scanner of the detecting device 4 scans the detecting barcode on the specimen tube, and scans the detected barcode and the attribute information of the detecting device 4 (detecting device information, for example, device model, device name, device) The information of the department, the device location, and the like is transmitted back to the data center 2, and the determining module 210 parses the detected device information in the returned detection barcode and performs comparison, if the detection device information in the detection barcode is returned to the detection device 4 Genus If the information is consistent, the determining module 210 determines that the liquid sample in the sample tube belongs to the detecting device 4, and the process proceeds to step S13. If the detecting device information in the detecting bar code is inconsistent with the attribute information returned by the detecting device 4, the determining module 210 It is determined that the liquid specimen in the specimen tube does not belong to the detection device 4, and the flow proceeds to step S12.

[0064] Step S12: When the liquid sample in the specimen tube does not belong to the detecting device 4, the sending module 220 sends the specimen tube detecting information (for example, the number, color, and the like of the specimen tube to be detected by the detecting device 4) to The detecting device 4 informs the inspector of the specimen tube corresponding to the detecting device 4, and notifies the detecting personnel to scan the corresponding specimen tube.

[0065] Step S13: The generating module 200 generates an initial status bar information and sends the information to the user terminal 5. In this embodiment, the start status bar information is used to indicate that the liquid sample detection in the sample tube has begun.

[0066] Step S14: When the detecting device 4 completes the detection of the liquid sample in the specimen tube and scans the detected barcode again, the transmitting module 220 generates an end status bar information and transmits the information to the user terminal 5. In this embodiment, the end status column information is used to indicate that the liquid sample detection in the specimen tube has ended.

[0067] Step S15: The determining module 210 determines whether each detected barcode has a corresponding initial status bar information and an end status bar information. If the detection bar code does not have a corresponding initial status bar information and an end status bar information, the determining module 210 determines that the detection item corresponding to the detection bar code has not been completed, and the flow returns to step S1. If each of the detection barcodes has a corresponding initial status bar information and an end status bar information, the determination module 210 determines that all the detection items have been completed in the detection prescription of the doctor, and the flow proceeds to step S16.

[0068] Step S16: The association module 230 acquires the detection result data of all the detecting devices 4 and generates a detection report, and associates the detection report with the electronic signature of the auditor. Specifically, the association module 230 receives the detection result data of all the detection devices 4 and puts them into the detection report template in the XML format to generate a detection report, and then associates the detection report with the electronic signature of the auditor.

[0069] Step S17: The sending module 220 sends the detection report to the doctor terminal 6 of the auditor for review. In the present embodiment, the auditor generally refers to a senior doctor (for example, a deputy chief physician or chief physician). It should be noted that the doctor terminal 6 of the auditor obtains the electronic signature of the auditor from the data center 2, and checks the sent test report by the obtained electronic signature verification. [0070] Step S18: The determining module 210 determines whether the test report is reviewed. Specifically, the determining module 210 sends the test report to the doctor terminal 6 of the auditor and pops up a confirmation dialog box. When the auditor clicks the confirmation button of the confirmation dialog box, it is determined that the auditor has reviewed the test report. The flow proceeds to step S19.

[0071] Step S19: The locking module 240 performs read-only locking on the detection report and generates a formal detection report.

Specifically, since the detection report is in an XML format, and the XML format includes various tags, the read-only locking of the detection result data can be completed by converting the tags of the corresponding regions in the XML. The manner in which the locking module 240 performs read-only locking on the detection report is as follows: The label name of the detection report template in the XML format is converted to complete the locking of the detection report. After the name conversion, the data in the label cannot be modified, edited, etc. After the conversion, due to the change of the labels of each level, even if the test report of Zhang San is modified, the corresponding data insertion position cannot be found in the detection report after the read-only lock, and the test report of Zhang San cannot be modified. . In addition, the formal test report also includes a two-dimensional code for the patient to scan through the two-dimensional code. The two-dimensional code includes basic information of the patient, and the generation method of the two-dimensional code is prior art, and details are not described herein.

The above are only the preferred embodiments of the present invention, and are not intended to limit the scope of the present invention, and the equivalent structure or equivalent process transformations made by the description of the present invention and the contents of the drawings may be directly or indirectly applied to other related The technical field is equally included in the scope of patent protection of the present invention.

Industrial applicability

[0073] The present invention adopts the above technical solution, and brings the technical effects as follows: The clinical inspection report review system and method based on barcode scanning according to the present invention detects the entire detection process by using a barcode, and notifies the user, It avoids human error in the detection process, ensures the transparent and controllable inspection process and the test result is correct, improves the detection efficiency and effectively reduces the medical accident caused by the mistake of clinical test, and can lock the test report and improve the test report. Information security.

Claims

Claim

A clinical inspection report review system based on bar code scanning, running in a data center, wherein the data center is connected to a user terminal, a doctor terminal, a barcode machine and a plurality of detecting devices through a network, the system comprising: a generating module, The utility model is configured to generate a detection barcode according to the detection medical order information and control the barcode printer to print the detection barcode; and a sending module, configured to: when the liquid specimen in the specimen tube does not belong to the detection device, send the specimen tube detection information to the detection device to notify the detecting personnel The detecting device corresponds to the specimen tube, and notifies the detecting personnel to scan the corresponding specimen tube; the generating module is configured to generate a start status bar information and send the information to the user terminal; and the sending module is configured to: when the detecting device completes the pair The detection of the liquid sample in the specimen tube and scanning the detection barcode again, generating the end status column information and transmitting to the user terminal; the association module is configured to have a corresponding initial status bar information and an end when each detection barcode has Status bar information 吋, get all checks The test result data of the device generates a test report, and associates the test report with the electronic signature of the auditor; the sending module is configured to send the test report to the doctor terminal of the auditor for review; and the locking module is used as the auditor The test report is reviewed, the test report is read-only, and a formal test report is generated.

The bar code scanning-based clinical test report review system according to claim 1, wherein the test bar code includes personal information of the user, doctor information, test item information, and test device information.

The bar code scanning-based clinical examination report review system according to claim 2, wherein if the detection device information in the detection bar code is consistent with the attribute information of the detection device, determining that the liquid sample in the sample tube belongs to the detection device Otherwise, if the detecting device information in the detecting bar code is inconsistent with the attribute device information of the detecting device, it is determined that the liquid sample in the sample tube does not belong to the detecting device.

The bar code scanning-based clinical test report review system according to claim 2, wherein the association module receives the test result data of all the detection devices and puts them into an XML-formatted test report template to complete the generation of the test report.

A bar code scanning based clinical test report review system according to claim 4, characterized in that The manner in which the locking module performs read-only locking on the detection result data is as follows: The label name corresponding to the detection result data in the detection report template of the X ML format is converted to complete the locking of the detection result data.

A method for reviewing a clinical test report based on bar code scanning is applied to a data center, wherein the data center is connected to a user terminal, a doctor terminal, a barcode machine and a plurality of detecting devices through a network, and the method comprises: The information generates a detection barcode and controls the barcode printer to print the detection barcode; when the liquid specimen in the specimen tube does not belong to the detection device, the specimen tube detection information is sent to the detection device to inform the inspector of the specimen tube corresponding to the detection device, and notify The inspector scans the corresponding specimen tube; generates an initial status bar information and sends it to the user terminal; when the detecting device completes the detection of the liquid sample in the specimen tube and scans the detected barcode again, generates an end status bar information and Send to the user terminal; when each detection bar code has a corresponding initial status bar information and an end status bar information, obtain detection result data of all detection devices and generate a detection report, and the detection report and the electronic signature of the auditor Chapter association; will check Send a report to the doctor terminal auditor's review; and when the audit staff of the inspection report have been reviewed, read-only lock, and generates a formal test report to the test report.

The barcode scanning-based clinical examination report review method according to claim 6, wherein the detection barcode includes personal information of the user, doctor information, detection item information, and detection device information.

The method for reviewing a clinical inspection report based on a bar code scanning according to claim 7, wherein if the detection device information in the detection bar code is consistent with the attribute information of the detection device, determining that the liquid sample in the sample tube belongs to the detection device Otherwise, if the detecting device information in the detecting bar code is inconsistent with the attribute device information of the detecting device, it is determined that the liquid sample in the sample tube does not belong to the detecting device.

The method for reviewing a clinical inspection report based on a barcode scanning according to claim 7, wherein the detection report is generated in the following manner: receiving detection result data of all detecting devices and putting them into a detection report template in an XML format to complete The generation of the test report. A bar code scanning based clinical test report review method according to claim 9, characterized in that The manner in which the locking module performs read-only locking on the detection result data is as follows: The label name corresponding to the detection result data in the detection report template of the X ML format is converted to complete the locking of the detection result data.