Auditing interface generation method

[0035] The technical solutions of the present invention will be further described in detail below through the accompanying drawings and embodiments.

[0036] Pharmacists need a simple, clear, and convenient prescription review interface for prescription suitability review, and the generation of the review interface needs to obtain different information from various interfaces as required, through the visual display of the first review information on the review interface, on the one hand It can avoid the wrong judgment caused by the incomplete consideration of the prescription pharmacist, and more importantly, it can greatly improve the efficiency of the prescription review by the prescription pharmacist.

[0037] The method for generating the audit interface of the present invention is used to realize the generation of different audit interfaces, thereby satisfying different audit requirements, and at the same time, optimizing the display content on the interface to improve the efficiency of the audit.

[0038] figure 1 It is a flowchart of the first embodiment of a method for generating an audit interface of the present invention. As shown in the figure, this embodiment specifically includes the following steps:

[0039] Step 101: Obtain the patient ID when the patient seeks medical attention in the hospital.

[0040] Specifically, the patient ID can be obtained when the patient seeks a doctor in the hospital by scanning the identity identifier such as the patient's wristband.

[0041] Step 102: Call the patient's basic patient information from the basic database by using the patient ID.

[0042] Specifically, the patient ID is used to call the basic patient information of the patient from the basic database, which specifically includes: patient number, name, age, gender, weight, height, body surface area, pregnancy, pregnancy, breastfeeding, allergy list, etc.

[0043] Step 103: Obtain prescription information of the patient ID.

[0044] The prescription information specifically refers to the detailed information of the drugs prescribed in all outpatient clinics after the outpatient clinic on the day.

[0045] Step 104: Extract drug information from the prescription information.

[0046] Extract the drug information used by the patient from the prescription information, including: drug name, specification, dosage, route of administration, frequency of administration, quantity, timing of administration, etc.

[0047] Step 105: Call the test information of the patient ID from the test database, and generate first link information of the test information.

[0048] Specifically, call various indicators of the patient test information corresponding to the patient ID from the test database, including: blood routine, blood biochemistry, blood coagulation function, immune index, urine routine, stool routine, etc., to generate the first link of the test information According to the link information, the actual data of the patient’s various test indicators can be viewed.

[0049] Step 106: Invoke the review related information from the rational drug use rule database, and generate second link information of the review related information.

[0050] Specifically, the review related information is other medical information that must be paid attention to when reviewing the patient's drug information, and the second link information of the review related point information is generated.

[0051] Call other medical information that must be paid attention to when reviewing the drug information of the patient from the rational drug use rule database, including image data such as electrocardiogram, ultrasound, X-ray, CT, magnetic resonance, etc., to generate the second link information of the review related point, according to the link You can view the actual data of other medical information when reviewing the patient’s drug information.

[0052] Step 107: Obtain review warning information generated after reviewing the drug information according to the rational drug use rules.

[0053] Specifically, according to the medication rules in the rational medication rule database, the warning information is automatically generated after the medication rationality of the patient's medication information is judged, and the alert information is obtained. The purpose is to facilitate the medication review pharmacist to obtain the preliminary review result of the patient's medication information. It is convenient for pharmacists to combine inspection information and other medical information to make more accurate and precise rationality judgments on patients' medication information, and to ensure the safety of patients' medications by adjusting prescriptions in time.

[0054] Step 108: Generate a first review information data set using the basic patient information, medication information, first link information of test information, second link information of review related information, and review warning information.

[0055] The first review information data set is generated from the various information of the patient obtained in the above steps.

[0056] Step 109: Generate a first audit interface using the first audit information data set.

[0057] The first audit information data set in step 108 is clearly displayed to generate the first audit interface, such as Figure 4 Shown.

[0058] The details of the outpatient prescription pharmacist review interface include: ①Basic patient information; ②Details of outpatient prescription drugs; ③Reasonable medication warning information; ④Test information link; ⑤Related point information. The inspection information and related point information can be viewed through the link. If the patient has multiple prescriptions on the same day, the details of each prescription shall be displayed under the same basic information of the patient. The prescription number, doctor, diagnosis, department, prescription time and other information must be displayed together with the drug details. The prescription review pharmacist can choose to prompt the doctor with the system warning information, or he can customize and edit the content prompted to the doctor after referring to the associated point information and the inspection information; click "pass", the prescription enters the next process, click "return", the system Return the pharmacist's treatment opinions to the prescribing doctor.

[0059] The method for generating an audit interface of the present invention uses various types of first audit information and second audit information to generate an information set, thereby achieving convenient, quick and reasonable display of the first audit information and second audit information.

[0060] figure 2 It is a flowchart of a second embodiment of a method for generating an audit interface of the present invention. As shown in the figure, this embodiment specifically includes the following steps:

[0061] Step 201: Obtain the patient ID when the patient seeks medical attention in the hospital.

[0062] Specifically, the patient ID can be obtained when the patient seeks a doctor in the hospital by scanning the patient's wristband and other identity identifiers.

[0063] Step 202: Call the patient's basic patient information from the basic database by using the patient ID.

[0064] Specifically, use the patient ID to call the basic patient information of the patient from the basic database, including: patient number, name, age, gender, weight, height, body surface area, whether you are pregnant, pregnancy, whether you are breastfeeding, list of allergies, and admission Department, admission time, diagnosis information, etc.

[0065] Step 203: Obtain the medical order information of the patient ID.

[0066] The medical order information is the detailed information of the medicine ordered by the hospital in the same day.

[0067] Step 204: Extract drug information from the medical order information.

[0068] Extract the drug information used by the patient from the medical order information, including: drug name, specification, single dose, usage, frequency, quantity, purpose of administration, start time, stop time, etc.

[0069] Step 205: Call the test information of the patient ID from the test database, and generate first link information of the test information.

[0070] Specifically, call various indicators of the patient test information corresponding to the patient ID from the test database, including: blood routine, blood biochemistry, blood coagulation function, immune index, urine routine, stool routine, etc., to generate the first link of the test information Information, according to the link information, the actual data of the patient’s various test indicators can be viewed.

[0071] Step 206: Invoke the audit related information from the rational drug use rule database, and generate second link information of the audit related information.

[0072] Specifically, the review related information is other medical information that must be paid attention to when reviewing the patient's drug information, and the second link information of the review related point information is generated.

[0073] Call other medical information that must be paid attention to when reviewing the drug information of the patient from the rational drug use rule database, including image data such as electrocardiogram, ultrasound, X-ray, CT, magnetic resonance, etc., to generate the second link information of the review related point, according to the link You can view the actual data of other medical information when reviewing the patient’s drug information.

[0074] Step 207: Obtain review warning information generated after reviewing the drug information according to the rational drug use rules.

[0075] Specifically, according to the medication rules in the rational medication rule database, the warning information is automatically generated after the medication rationality of the patient's medication information is judged, and the alert information is obtained. The purpose is to facilitate the medication review pharmacist to obtain the preliminary review result of the patient's medication information. It is convenient for pharmacists to combine inspection information and other medical information to make more accurate and precise rationality judgments on patients' medication information, and to ensure the safety of patients' medications by adjusting prescriptions in time.

[0076] Step 208: Generate a first review information data set using the basic patient information, medication information, first link information of test information, second link information of review related information, and review warning information.

[0077] The first review information data set is generated from the various information of the patient obtained in the above steps.

[0078] Step 209: Generate a first audit interface using the first audit information data set.

[0079] The first audit information data set in step 208 is clearly displayed to generate the first audit interface, such as Figure 5 Shown.

[0080] Intercept the medication details of hospitalized patients on any day in the hospital, and the detailed display of the pharmacist review interface includes: ①Basic information of the patient; ②Details of the medication used by the inpatient on a certain day; ③Rational medication warning information; ④Test information link; ⑤Related point information. The review interface displays the drug order details that are valid on the day after the merger. Click the test information to display the latest test information of the intercepted medical order. The related point information can be viewed through the link after the corresponding drug is selected. The rational drug use warning information shows the drug use warnings on the day of the interception. The prescription pharmacist can choose to remind the doctor of the system warning information, or he can customize the content of the warning to the doctor after referring to the related point information and the inspection information. Click "Approve", the doctor's order will enter the next process. If the immediate doctor's order (that is, the same day) is reviewed, click "Return", and the system will return the pharmacist's treatment comments to the doctor; if the historical doctor's order is reviewed, clicking "Return" is invalid .

[0081] This embodiment is an example of the cross-sectional review of hospital order information. The cross-sectional review is based on each day of hospitalization of the hospitalized patient as a cross-section. The pharmacist review interface displays all the drugs used by the patient on that day, and completes the review and review of related points. A cross-sectional review of all medication orders of the patient. This review method is particularly suitable for real-time review, evaluation and analysis of the medication process.

[0082] The review of medication rationality of inpatient medical orders has the characteristics of multiple types of medications, many influencing factors of medication, and long diagnosis and treatment cycles. The inpatient medication review function mainly realizes: (1) Clear display of medication orders; (2) Display of medication-related non-drug orders; (3) Display of medication-related test results; (4) Display of medication warning information; (5) Display of medication-related unstructured information.

[0083] In addition, in accordance with different review requirements for hospital orders, the present invention can also conduct a combined review of the patient's current effective medication orders or conduct a combined review of the medications in the entire treatment process.

[0084] The method for generating the audit interface of the present invention uses various types of first audit information and second audit information to generate an information set, thereby achieving convenient, quick and reasonable display of the first audit information and second audit information.

[0085] image 3 It is a flowchart of a third embodiment of a method for generating an audit interface of the present invention. As shown in the figure, this embodiment specifically includes the following steps:

[0086] Step 301: Obtain the patient ID when the patient seeks medical attention in the hospital.

[0087] Specifically, the patient ID can be obtained when the patient seeks a doctor in the hospital by scanning the patient's wristband and other identity identifiers.

[0088] Step 302: Use the patient ID to call the basic patient information of the patient from the basic database.

[0089] Specifically, use the patient ID to call the basic patient information of the patient from the basic database, including: patient number, name, age, gender, weight, height, body surface area, whether you are pregnant, pregnancy, whether you are breastfeeding, list of allergies, and admission Department, admission time, etc.

[0090] Step 303: Obtain the prescription/doctor's order information of the patient ID.

[0091] Obtain the prescription information/doctor's order information during the entire process from admission to discharge corresponding to the patient ID.

[0092] Step 304: Extract drug information from the prescription/doctor's order information.

[0093] Extract the medication information from the medication record of the patient from admission to discharge.

[0094] In step 305, the medication sequence information is generated according to the time axis sequence of the medication detailed information of each day's hospital prescription.

[0095] Step 306: Use the medical order information to generate medical order link information.

[0096] Step 307: Obtain diagnosis time point information, test time point information, and vital sign recording point information.

[0097] Step 308: Use the time point information corresponding to the diagnostic information to generate diagnostic information link information, use the time point information corresponding to the test information to generate test information link information, and use the vital sign record point information to generate vital sign record information link information .

[0098] Step 309: Use the medical order link information, diagnosis information link information, test information link information, and vital sign record information link information to generate a second review information data set.

[0099] Step 310: Generate a second audit interface using the second audit information data set.

[0100] This example is an example of the review of the inpatient order process. The pharmacist review interface displays the patient's medication records from admission to discharge, and combines relevant review points to deal with the patient's entire medication plan, medication process, and medication related events Conduct reasonable review and evaluation. It is also possible to select a certain section to conduct reasonable review and evaluation of the medication in the process before the section. The review process is a retrospective review.

[0101] Process review is the timeline of the patient’s medical order list on the pharmacist’s review interface showing all the medicines used during the patient’s hospitalization, including valid and expired medical orders. If the patient has been discharged, it will show all the medicines used by the patient during the hospitalization. , In addition, the time points recorded by diagnosis, test and vital signs are also displayed on the interface, such as Image 6 Shown. Click the corresponding diagnosis time point to display the diagnosis information and corrected diagnosis information; click the test time point to display the test report information of the click day; click the vital sign time point to display the vital sign curve; click the start time point of the drug order, you can Display the detailed information of the medication order.

[0102] For the use of timeline to show patients’ inpatient medications, the medication plan can be reviewed, including the combination of medications, the order of medication, the duration of medication, and the use of corresponding auxiliary medications, completing the entire management of patients .

[0103] Compared with the prior art, the present invention can combine different audit requirements, display the content to be audited on the audit interface according to section and process, and at the same time provide comprehensively the important related points required in the prescription/doctor order audit on the interface The information is conducive to prescription review pharmacists to make correct judgments immediately and efficiently.

[0104] Professionals should also be further aware that the units and algorithm steps of the examples described in the embodiments disclosed in this article can be implemented by electronic hardware, computer software or a combination of both, in order to clearly illustrate the hardware and software Interchangeability. In the above description, the composition and steps of each example have been generally described in accordance with the function. Whether these functions are executed by hardware or software depends on the specific application and design constraints of the technical solution. Professionals and technicians can use different methods for each specific application to implement the described functions, but such implementation should not be considered as going beyond the scope of the present invention.

[0105] The steps of the method or algorithm described in combination with the embodiments disclosed herein can be implemented by hardware, a software module executed by a processor, or a combination of the two. The software module can be placed in random access memory (RAM), internal memory, read-only memory (ROM), electrically programmable ROM, electrically erasable programmable ROM, registers, hard disks, removable disks, CD-ROMs, or all areas in the technical field. Any other known storage media.

[0106] The specific embodiments described above further describe the purpose, technical solutions and beneficial effects of the present invention in further detail. It should be understood that the above descriptions are only specific embodiments of the present invention and are not intended to limit the scope of the present invention. The protection scope, any modification, equivalent replacement, improvement, etc. made within the spirit and principle of the present invention shall be included in the protection scope of the present invention.