Confirmation method and device of responsibility department, electronic equipment and computer storage medium
The method and device determine the responsible department for medical records by querying electronic medical records using a patient's identifier and comparing creation times with transfer times, enabling accurate and timely rectification notices.
Patent Information
- Application Number
- CN202410889111.6
- Authority / Receiving Office
- CN · China
- Patent Type
- Applications(China)
- Current Assignee / Owner
- Filing Date
- 2024-07-03
- Publication Date
- 2024-12-27
AI Technical Summary
Determining the responsible department for medical record quality control is challenging due to patient transfers between departments, leading to inaccurate rectification messages.
A method and device that utilize a patient's unique identifier to query electronic medical records, determine document creation departments by comparing document creation times with transfer times, and generate rectification notices based on quality control results.
Effectively identifies the responsible department for medical record quality control, ensuring accurate and timely rectification notices are sent.
Smart Images
Figure CN119207737A_ABST
Abstract
Description
Technical Field
[0001] The present application relates to the field of medical information technology, and in particular to a method, device, electronic equipment and computer storage medium for confirming a responsible department. Background Art
[0002] As people's demands for health levels continue to improve and medical practices become more standardized, medical records that record medical practices must be true, accurate, timely and complete, and any errors must be corrected in a timely manner.
[0003] During the treatment process, inpatients may need to be transferred to other departments for diagnosis and treatment due to their condition, and the medical records recording the patient's condition are written by doctors from multiple departments. During the medical record quality control process, medical record defects need to be sent to the responsible department for rectification. Due to the transfer of departments, it is difficult to determine the responsible department and the rectification message sent is inaccurate. Summary of the invention
[0004] In view of this, the present application provides a method, device, electronic device and computer storage medium for confirming the responsible department, so that the responsible department can be effectively determined during the medical record quality control process.
[0005] The first aspect of the present application provides a method for confirming a responsible department, comprising:
[0006] Receiving a quality control request; wherein the quality control request includes: a unique identification of a patient;
[0007] Querying the electronic medical record system according to the patient's unique identifier to obtain detailed information on all documents of the patient; wherein the detailed information on the document includes the document name and the department where the document was created;
[0008] Receive quality control results and generate rectification notices based on the quality control results and detailed information of the documents; the quality control results include: defect items, defect details and deductions.
[0009] Optionally, the method for generating detailed information of the document includes:
[0010] Acquire the patient's department transfer information in the hospital information system; wherein the department transfer information includes: the transfer target department, the transfer target department code, the transfer time, the original department and the original department code;
[0011] Obtaining document information of all documents of the patient in the electronic medical record system; wherein the document information of the document includes: document name, document unique identification mark, and document creation time;
[0012] For each document, according to the document information and the department transfer information of the document, determine the document creation department of the document;
[0013] By using the unique identification mark of the document, the document creation department of the document is added to the document information of the document to obtain detailed information of the document.
[0014] Optionally, for each document, determining the document creation department of the document according to the document information of the document and the department transfer information includes:
[0015] The department in which the document was created is obtained by comparing the creation time of the document with the transfer time.
[0016] Optionally, the step of comparing the document creation time of the document with the department transfer time to obtain the document creation department of the document includes:
[0017] Sort all transfer times in descending order;
[0018] Determine whether the document creation time is greater than or equal to the subject transfer time;
[0019] If it is determined that the document creation time is greater than or equal to the department transfer time, the department corresponding to the first department transfer time whose document creation time is greater than or equal to the department transfer time is used as the document creation department of the document;
[0020] If it is determined that the document creation time is less than the department transfer time, the admission department will be used as the document creation department.
[0021] The second aspect of the present application provides a responsible department confirmation device, comprising:
[0022] A receiving unit, configured to receive a quality control request; wherein the quality control request includes: a unique identification of a patient;
[0023] A query unit, used for querying and obtaining detailed information of all documents of the patient in the electronic medical record system according to the unique identifier of the patient; wherein the detailed information of the document includes the name of the document and the department where the document was created;
[0024] The generating unit is used to receive the quality control results and generate a rectification notice according to the quality control results and the detailed information of the document; wherein the quality control results include: defect items, defect details and deduction points.
[0025] Optionally, the unit for generating detailed information of the document includes:
[0026] The first acquisition unit is used to acquire the patient's department transfer information in the hospital information system; wherein the department transfer information includes: the transfer target department, the transfer target department code, the transfer time, the original department and the original department code;
[0027] The second acquisition unit is used to acquire document information of all documents of the patient in the electronic medical record system; wherein the document information of the document includes: document name, document unique identification mark, and document creation time;
[0028] A determination unit, for determining, for each document, a document creation department of the document according to the document information of the document and the department transfer information;
[0029] The adding unit is used to add the document creation department of the document to the document information of the document through the unique identification mark of the document to obtain detailed information of the document.
[0030] Optionally, the determining unit includes:
[0031] The comparison unit is used to compare the document creation time of the document with the department transfer time to obtain the document creation department of the document.
[0032] Optionally, the comparison unit includes:
[0033] A sorting unit is used to sort all transfer times in descending order;
[0034] A judgment unit, used to judge whether the document creation time is greater than or equal to the course transfer time;
[0035] a document creation department determination unit, configured to, if the determination unit determines that the document creation time is greater than or equal to the department transfer time, use the department corresponding to the first department transfer time whose document creation time is greater than or equal to the department transfer time as the document creation department of the document;
[0036] The document creation department determination unit is further used to use the admission department as the document creation department of the document if the determination unit determines that the document creation time is less than the department transfer time.
[0037] A third aspect of the present application provides an electronic device, including:
[0038] one or more processors;
[0039] a storage device having one or more programs stored thereon;
[0040] When the one or more programs are executed by the one or more processors, the one or more processors implement the responsible department confirmation method as described in any one of the first aspects.
[0041] A fourth aspect of the present application provides a computer storage medium having a computer program stored thereon, wherein when the computer program is executed by a processor, the method for confirming a responsible department as described in any one of the first aspects is implemented.
[0042] It can be seen from the above scheme that the present application provides a method, device, electronic device and computer storage medium for confirming the responsible department. After receiving the quality control request, the detailed information of all the patient's documents are queried in the electronic medical record system according to the patient's unique identifier in the quality control request, and then the quality control results are obtained; wherein the quality control results include: defective items, defect details and deductions; finally, after receiving the quality control results, a rectification notice is generated according to the quality control results and the document name and document creation department in the detailed information of the document, so that the responsible department can be effectively determined. BRIEF DESCRIPTION OF THE DRAWINGS
[0043] In order to more clearly illustrate the embodiments of the present invention or the technical solutions in the prior art, the drawings required for use in the embodiments or the description of the prior art will be briefly introduced below. Obviously, the drawings described below are only embodiments of the present invention. For ordinary technicians in this field, other drawings can be obtained based on the provided drawings without paying creative work.
[0044] Figure 1 A specific flow chart of a method for confirming a responsible department provided in an embodiment of the present application;
[0045] Figure 2 A schematic diagram of a quality control result provided in another embodiment of the present application;
[0046] Figure 3 A flowchart of a method for generating detailed information of a document provided in another embodiment of the present application;
[0047] Figure 4 A schematic diagram of a case transfer information provided by another embodiment of the present application;
[0048] Figure 5 A schematic diagram of department transfer information of a discharged medical record provided in another embodiment of the present application;
[0049] Figure 6 A schematic diagram of a document creation time for recording an admission record provided by another embodiment of the present application;
[0050] Figure 7 A schematic diagram of a document creation time for recording a medical record provided by another embodiment of the present application;
[0051] Figure 8 A schematic diagram of a document creation time for recording a medical record provided by another embodiment of the present application;
[0052] Fig. 9 A schematic diagram of a document creation time for recording a discharge record provided by another embodiment of the present application;
[0053] Fig.10 A flowchart of a method for determining a document creation department of a document provided in another embodiment of the present application;
[0054] Fig.11 A schematic diagram of a confirmation device for a responsible department provided in another embodiment of the present application;
[0055] Fig.12 A schematic diagram of an electronic device for implementing a method for confirming a responsible department provided in another embodiment of the present application. DETAILED DESCRIPTION
[0056] The following will be combined with the drawings in the embodiments of the present invention to clearly and completely describe the technical solutions in the embodiments of the present invention. Obviously, the described embodiments are only part of the embodiments of the present invention, not all of the embodiments. Based on the embodiments of the present invention, all other embodiments obtained by ordinary technicians in this field without creative work are within the scope of protection of the present invention.
[0057] It should be noted that the information (including but not limited to user device information, user personal information, etc.) and data (including but not limited to data used for analysis, stored data, displayed data, etc.) involved in this application are all information and data authorized by the user or fully authorized by all parties, and the collection, use and processing of relevant data must comply with relevant laws, regulations and standards of relevant countries and regions.
[0058] The term "including" and its variations used herein are open inclusions, i.e., "including but not limited to". The term "based on" means "based at least in part on". The term "one embodiment" means "at least one embodiment"; the term "another embodiment" means "at least one additional embodiment"; the term "some embodiments" means "at least some embodiments". The relevant definitions of other terms will be given in the following description.
[0059] It should be noted that the concepts such as "first" and "second" mentioned in this application are only used to distinguish different devices, modules or units, and are not used to limit the order or interdependence of the functions performed by these devices, modules or units.
[0060] It should be noted that the modifications of "one" and "plurality" mentioned in the present application are illustrative rather than restrictive, and those skilled in the art should understand that unless otherwise clearly indicated in the context, it should be understood as "one or more".
[0061] First, the technical terms appearing in this application are explained:
[0062] Hospital Information System (His): refers to an information system that uses modern means such as computer software and hardware technology and network communication technology to comprehensively manage the flow of personnel, logistics, and finances in a hospital and its affiliated departments, collect, store, process, extract, transmit, and summarize data generated at various stages of medical activities, and process them into various information, thereby providing comprehensive automated management and various services for the overall operation of the hospital.
[0063] Electronic medical record (EMR): refers to the digital medical record stored, managed, transmitted and reproduced by electronic devices (computers, health cards, etc.) to replace the handwritten paper medical record. Its content includes all the information of the paper medical record. The National Institute of Medicine of the United States defines it as: EMR is an electronic patient record based on a specific system that provides users with access to complete and accurate data, warnings, prompts and clinical decision support systems.
[0064] The present application embodiment provides a method for confirming the responsible department, such as Figure 1 As shown, the specific steps include:
[0065] S101. Receive a quality control request.
[0066] Among them, the quality control request includes: the patient's unique identification.
[0067] During the specific implementation of this application, quality control personnel can search for all the patient's medical information on the system based on the patient's unique identifier, where the medical information includes hospitalization information, outpatient information, emergency information, etc.
[0068] S102. Query the electronic medical record system according to the patient's unique identifier to obtain detailed information on all documents that have passed the patient.
[0069] Among them, the detailed information of the document includes the name of the document and the department that created the document.
[0070] In the specific implementation process of this application, detailed information of all documents of the patient can also be found according to the medical record number, which is not limited here.
[0071] S103. Receive the quality control results and generate a rectification notice based on the quality control results and detailed information of the document.
[0072] The quality control results include: defect items, defect details and deductions. The quality control results can be filled in and modified by relevant authorized staff, etc., and there is no limitation here.
[0073] like Figure 2As shown, it is a schematic diagram of a quality control result provided in this application. It can be seen that the document named Postoperative Pathology Record was created by the Urology Department, the defective item is the lack of medical records for 3 consecutive days after surgery, and the defect details are that the medical records for the first day after surgery were not completed in time..., and the deduction is 1 point; the document named Preoperative Discussion was created by the Critical Care Medicine Department, the defective item is the lack of preoperative discussion records..., the defect details are that the preoperative discussion was not completed before surgery..., and the deduction is 25 points.
[0074] During the specific implementation of this application, a rectification notice can be automatically generated based on the quality control results and detailed information of the document, and the rectification notice can be sent to the department that needs rectification.
[0075] Optionally, in another embodiment of the present application, an implementation method of a method for generating detailed information of a document is as follows: Figure 3 As shown, including:
[0076] S301. Obtain the patient's department transfer information in the hospital information system.
[0077] The transfer information includes: the target department, the target department code, the transfer time, the original department and the original department code.
[0078] See also Figure 4 A schematic diagram of the transfer information of a running case provided for this application, see Figure 5 A schematic diagram of the transfer information of a discharge medical record provided for this application shows that the transfer information records in detail the transfer target department, the transfer target department code, the transfer time, the original department and the original department code.
[0079] S302: Obtain document information of all documents of the patient in the electronic medical record system.
[0080] Among them, the document information of the document includes: document name, document unique identification mark, and document creation time.
[0081] like Figures 6 to 9 As shown, in the implementation process of the present application, the creation time of the admission record, medical record, discharge record, etc. can be recorded in the document but is not limited to it.
[0082] S303. For each document, determine the document creation department based on the document information and department transfer information of the document.
[0083] Optionally, in another embodiment of the present application, an implementation of step S303 specifically includes:
[0084] By comparing the document's creation time and transfer time, the department in which the document was created can be obtained.
[0085] Specifically, since there may be multiple department transfers, the clerk's document creation time is compared with all department transfer times, and the clerk's document creation department is determined based on the time range of all department transfer times.
[0086] Optionally, in another embodiment of the present application, an implementation method of obtaining the document creation department of the document is performed by comparing the document creation time and the department transfer time of the document, such as Fig.10 As shown, specifically including:
[0087] S1001. Sort all transfer times in descending order.
[0088] In the specific implementation process of this application, all transfer times can be sorted in descending order and organized into a table, which is not limited here, such as Table 1:
[0089] time state Department 2023-12-1811 Discharge Emergency Department 2023-12-1117 Transfer Emergency Department 2023-12-0818 Transfer Critical Care Medicine 2023-12-0814 Admission Emergency Department
[0090] Table 1
[0091] S1002. Determine whether the document creation time is greater than or equal to the subject transfer time.
[0092] Specifically, if it is determined that the document creation time is greater than or equal to the transfer time, execute step S1003; if it is determined that the document creation time is less than the transfer time (that is, there is no transfer time when the document creation time is queried downward), execute step S1004.
[0093] S1003. The department corresponding to the first department transfer time whose document creation time is greater than or equal to the department transfer time is used as the document creation department of the document.
[0094] S1004. Create a department with the admission department as the clerical department.
[0095] For example: As shown in Table 2, the first transfer time after the document creation time is taken, and the corresponding department is the creation department.
[0096] The first time after the discharge record creation time [2023-12-1815] is [2023-12-1811], and the corresponding department is the emergency department.
[0097] The creation time of the admission record is [2023-12-0809]. If there is no smaller time, the last one is taken, that is, the emergency department of the hospital is used as the creation department.
[0098] Document creation time Documents Create a department time state Department 2023-12-1815 Discharge Record Emergency Department 2023-12-1811 Discharge Emergency Department 2023-12-1409 Medical records Emergency Department 2023-12-1117 Transfer Emergency Department 2023-12-0906 Medical records Critical Care Medicine 2023-12-0818 Transfer Critical Care Medicine 2023-12-0809 Admission records Emergency Department 2023-12-0814 Admission Emergency Department
[0099] Table 2
[0100] In the specific implementation process of this application, the specific judgment logic can be as follows:
[0101] 1. Input parameters include pid#vid (patient unique identifier) and createTime (creation time);
[0102] 2. There is a department transfer information table zhuanke_table, which contains the fields pid#vid, zrtime (transfer time), dept_name (department name);
[0103] 3. Through pid#vid, you can associate it with the transfer information table zhuanke_table and add the filter condition createTime>=zrtime;
[0104] 4. Get the matching number result num;
[0105] 5. When num>0, only the first result is taken (orderby sorted in descending order), and the dept_name of the transfer information table zhuanke_table is returned;
[0106] 6. If num=0, then pid#vid can be used to associate with the hospital admission registration table ruyuan_table (generally, there is only one entry for each patient's hospitalization) and obtain the matching quantity result num;
[0107] 7. When num>0, only the first result is taken and the dept_name of the admission registration table ruyuan_table is returned; if num=0, "null" is returned.
[0108] S304. By using the unique identification mark of the document, the document creation department of the document is added to the document information of the document to obtain detailed information of the document.
[0109] In the specific implementation process of this application, after obtaining the detailed information of the document, the detailed information of the document will be written into the medical record database.
[0110] It can be seen from the above scheme that the present application provides a method for confirming the responsible department. After receiving the quality control request, the detailed information of all the patient's documents is queried in the electronic medical record system according to the patient's unique identifier in the quality control request, and then the quality control result is obtained; wherein the quality control result includes: defective items, defect details and deductions; finally, after receiving the quality control result, a rectification notice is generated according to the quality control result and the document name and document creation department in the detailed information of the document, so that the responsible department can be effectively determined.
[0111] Another embodiment of the present application provides a confirmation device for a responsible department, such as Fig.11 As shown, specifically including:
[0112] The receiving unit 1101 is used to receive a quality control request.
[0113] Among them, the quality control request includes: the patient's unique identification.
[0114] The query unit 1102 is used to query the electronic medical record system to obtain detailed information of all documents of the patient according to the patient's unique identifier.
[0115] Among them, the detailed information of the document includes the name of the document and the department that created the document.
[0116] The generating unit 1103 is used to receive the quality control result and generate a rectification notice according to the quality control result and the detailed information of the document.
[0117] Among them, the quality control results include: defect items, defect details and deduction points.
[0118] For the specific working process of the units disclosed in the above embodiments of the present application, please refer to the corresponding method embodiments, such as Figure 1 As shown, no further description is given here.
[0119] Optionally, in another embodiment of the present application, an implementation of a unit for generating detailed information of a document includes:
[0120] The first acquisition unit is used to acquire the patient's department transfer information in the hospital information system.
[0121] The transfer information includes: the target department, the target department code, the transfer time, the original department and the original department code.
[0122] The second acquisition unit is used to acquire document information of all documents of the patient in the electronic medical record system.
[0123] Among them, the document information of the document includes: document name, document unique identification mark, and document creation time.
[0124] The determination unit is used to determine the document creation department for each document according to the document information and department transfer information of the document.
[0125] The adding unit is used to add the document creation department of the document to the document information of the document through the unique identification mark of the document to obtain the detailed information of the document.
[0126] For the specific working process of the units disclosed in the above embodiments of the present application, please refer to the corresponding method embodiments, such as Figure 3 As shown, no further description is given here.
[0127] Optionally, in another embodiment of the present application, an implementation of the determination unit specifically includes:
[0128] The comparison unit is used to compare the document creation time and the department transfer time of the document to obtain the document creation department of the document.
[0129] The specific working process of the units disclosed in the above embodiments of the present application can be found in the corresponding method embodiments, which will not be repeated here.
[0130] Optionally, in another embodiment of the present application, an implementation of the comparison unit specifically includes:
[0131] Sorting unit, used to sort all transfer times in descending order.
[0132] The judgment unit is used to judge whether the document creation time is greater than or equal to the subject transfer time.
[0133] The document creation department determination unit is used to use the department corresponding to the first transfer time whose document creation time is greater than or equal to the transfer time as the document creation department of the document if the judgment unit determines that the document creation time is greater than or equal to the transfer time.
[0134] The document creation department determination unit is also used to use the admission department as the document creation department for the document if the judgment unit determines that the document creation time is less than the transfer department time.
[0135] For the specific working process of the units disclosed in the above embodiments of the present application, please refer to the corresponding method embodiments, such as Fig.10 As shown, no further description is given here.
[0136] It can be seen from the above scheme that the present application provides a confirmation device for the responsible department. After receiving the quality control request, the detailed information of all the patient's documents is queried in the electronic medical record system according to the patient's unique identifier in the quality control request, and then the quality control result is obtained; wherein the quality control result includes: defective items, defect details and deductions; finally, after receiving the quality control result, a rectification notice is generated according to the quality control result and the document name and document creation department in the detailed information of the document, so that the responsible department can be effectively determined.
[0137] The functions described above herein may be performed at least in part by one or more hardware logic components. For example, without limitation, exemplary types of hardware logic components that may be used include: field programmable gate arrays (FPGAs), application specific integrated circuits (ASICs), application specific standard products (ASSPs), systems on chips (SOCs), complex programmable logic devices (CPLDs), and the like.
[0138] Another embodiment of the present application provides an electronic device, such as Fig.12 As shown, including:
[0139] One or more processors 1201.
[0140] The storage device 1202 stores one or more programs.
[0141] When one or more programs are executed by one or more processors 1201, one or more processors 1201 implement a method for confirming a responsible department as described in any one of the above embodiments.
[0142] Another embodiment of the present application provides a computer storage medium having a computer program stored thereon, wherein when the computer program is executed by a processor, the method for confirming the responsible department as described in any one of the above embodiments is implemented.
[0143] In the context of the present application, a machine-readable medium may be a tangible medium that may contain or store a program for use by or in conjunction with an instruction execution system, device, or equipment. A machine-readable medium may be a machine-readable signal medium or a machine-readable storage medium. A machine-readable medium may include, but is not limited to, an electronic, magnetic, optical, electromagnetic, infrared, or semiconductor system, device, or equipment, or any suitable combination of the foregoing. A more specific example of a machine-readable storage medium may include an electrical connection based on one or more lines, a portable computer disk, a hard disk, a random access memory (RAM), a read-only memory (ROM), an erasable programmable read-only memory (EPROM or flash memory), an optical fiber, a portable compact disk read-only memory (CD-ROM), an optical storage device, a magnetic storage device, or any suitable combination of the foregoing.
[0144] It should be noted that the computer-readable medium mentioned above in the present application may be a computer-readable signal medium or a computer-readable storage medium or any combination of the above two. The computer-readable storage medium may be, for example, but not limited to, an electrical, magnetic, optical, electromagnetic, infrared, or semiconductor system, device or device, or any combination of the above. More specific examples of computer-readable storage media may include, but are not limited to: an electrical connection with one or more wires, a portable computer disk, a hard disk, a random access memory (RAM), a read-only memory (ROM), an erasable programmable read-only memory (EPROM or flash memory), an optical fiber, a portable compact disk read-only memory (CD-ROM), an optical storage device, a magnetic storage device, or any suitable combination of the above. In the present application, a computer-readable storage medium may be any tangible medium containing or storing a program that can be used by or in combination with an instruction execution system, device or device. In the present application, a computer-readable signal medium may include a data signal propagated in a baseband or as part of a carrier wave, in which a computer-readable program code is carried. This propagated data signal may take a variety of forms, including but not limited to electromagnetic signals, optical signals, or any suitable combination of the above. The computer readable signal medium may also be any computer readable medium other than a computer readable storage medium, which may send, propagate or transmit a program for use by or in conjunction with an instruction execution system, apparatus or device. The program code contained on the computer readable medium may be transmitted using any suitable medium, including but not limited to: wires, optical cables, RF (radio frequency), etc., or any suitable combination of the above.
[0145] The computer-readable medium may be included in the electronic device, or may exist independently without being incorporated into the electronic device.
[0146] Another embodiment of the present application provides a computer program product, which, when executed, is used to execute any of the above-mentioned methods for confirming the responsible department.
[0147] In particular, according to an embodiment of the present application, the process described above with reference to the flowchart can be implemented as a computer software program. For example, an embodiment of the present application includes a computer program product, which includes a computer program carried on a non-transitory computer-readable medium, and the computer program includes a program code for executing the method shown in the flowchart. In such an embodiment, the computer program can be downloaded and installed from a network via a communication device, or installed from a storage device, or installed from a ROM. When the computer program is executed by a processing device, the above-mentioned functions defined in the method of the embodiment of the present application are executed.
[0148] Although the subject matter has been described in language specific to structural features and / or methodological logical actions, it should be understood that the subject matter defined in the appended claims is not necessarily limited to the specific features or actions described above. On the contrary, the specific features and actions described above are merely example forms of implementing the claims.
[0149] Although several specific implementation details are included in the above discussion, these should not be interpreted as limiting the scope of the present application. Certain features described in the context of a separate embodiment can also be implemented in a single embodiment in combination. On the contrary, the various features described in the context of a single embodiment can also be implemented in multiple embodiments individually or in any suitable sub-combination.
[0150] The above description is only a preferred embodiment of the present application and an explanation of the technical principles used. Those skilled in the art should understand that the scope of application involved in the present application is not limited to the technical solution formed by a specific combination of the above technical features, but should also cover other technical solutions formed by any combination of the above technical features or their equivalent features without departing from the above application concept. For example, the above features are replaced with (but not limited to) technical features with similar functions applied in the present application.
Claims
1. A method for confirming a responsible department, characterized in that: include: Receiving a quality control request; wherein the quality control request includes: a unique identification of a patient; Querying the electronic medical record system according to the patient's unique identifier to obtain detailed information of all documents of the patient; wherein the detailed information of the document includes the document name and the department where the document was created; Receive quality control results and generate rectification notices based on the quality control results and detailed information of the documents; the quality control results include: defect items, defect details and deductions.
2. The method for confirming the responsible department according to claim 1, characterized in that: The method for generating detailed information of the document includes: Acquire the patient's department transfer information in the hospital information system; wherein the department transfer information includes: the transfer target department, the transfer target department code, the transfer time, the original department and the original department code; Obtaining document information of all documents of the patient in the electronic medical record system; wherein the document information of the document includes: document name, document unique identification mark, and document creation time; For each document, according to the document information and the department transfer information of the document, determine the document creation department of the document; By using the unique identification mark of the document, the document creation department of the document is added to the document information of the document to obtain detailed information of the document.
3. The method for confirming the responsible department according to claim 2, characterized in that: For each document, according to the document information of the document and the department transfer information, determining the document creation department of the document includes: The department in which the document was created is obtained by comparing the creation time of the document with the transfer time.
4. The method for confirming the responsible department according to claim 3, characterized in that: The step of comparing the document creation time of the document with the department transfer time to obtain the document creation department of the document includes: Sort all transfer times in descending order; Determine whether the document creation time is greater than or equal to the subject transfer time; If it is determined that the document creation time is greater than or equal to the department transfer time, the department corresponding to the first department transfer time whose document creation time is greater than or equal to the department transfer time is used as the document creation department of the document; If it is determined that the document creation time is less than the department transfer time, the admission department will be used as the document creation department.
5. A confirmation device for a responsible department, characterized in that: include: A receiving unit, configured to receive a quality control request; wherein the quality control request includes: a unique identification of a patient; A query unit, used for querying and obtaining detailed information of all documents of the patient in the electronic medical record system according to the unique identifier of the patient; wherein the detailed information of the document includes the name of the document and the department where the document was created; A generating unit is used to receive the quality control results and generate a rectification notice according to the quality control results and detailed information of the document; wherein the quality control results include: defect items, defect details and deduction points.
6. The responsible department confirmation device according to claim 5, characterized in that: The unit for generating detailed information of the document includes: The first acquisition unit is used to acquire the patient's department transfer information in the hospital information system; wherein the department transfer information includes: the transfer target department, the transfer target department code, the transfer time, the original department and the original department code; The second acquisition unit is used to acquire document information of all documents of the patient in the electronic medical record system; wherein the document information of the document includes: document name, document unique identification mark, and document creation time; A determination unit, for determining, for each document, a document creation department of the document according to the document information of the document and the department transfer information; The adding unit is used to add the document creation department of the document to the document information of the document through the unique identification mark of the document to obtain detailed information of the document.
7. The responsible department confirmation device according to claim 6, characterized in that: The determining unit comprises: The comparison unit is used to compare the document creation time of the document with the department transfer time to obtain the document creation department of the document.
8. The responsible department confirmation device according to claim 7, characterized in that: The comparison unit comprises: A sorting unit is used to sort all transfer times in descending order; A judgment unit, used to judge whether the document creation time is greater than or equal to the course transfer time; a document creation department determination unit, configured to, if the determination unit determines that the document creation time is greater than or equal to the department transfer time, use the department corresponding to the first department transfer time whose document creation time is greater than or equal to the department transfer time as the document creation department of the document; The document creation department determination unit is further used to use the admission department as the document creation department of the document if the determination unit determines that the document creation time is less than the department transfer time.
9. An electronic device, characterized in that: include: one or more processors; a storage device having one or more programs stored thereon; When the one or more programs are executed by the one or more processors, the one or more processors implement the responsible department confirmation method as described in any one of claims 1 to 4.
10. A computer storage medium, characterized in that: A computer program is stored thereon, wherein when the computer program is executed by a processor, the method for confirming the responsible department as described in any one of claims 1 to 4 is implemented.