CN113392626A - Method and device for generating medical document and storage medium - Google Patents
Method and device for generating medical document and storage medium Download PDFInfo
- Publication number
- CN113392626A CN113392626A CN202110690182.XA CN202110690182A CN113392626A CN 113392626 A CN113392626 A CN 113392626A CN 202110690182 A CN202110690182 A CN 202110690182A CN 113392626 A CN113392626 A CN 113392626A
- Authority
- CN
- China
- Prior art keywords
- document
- generating
- field
- preset
- original structural
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
- 238000000034 method Methods 0.000 title claims abstract description 49
- 238000013507 mapping Methods 0.000 claims description 13
- 239000012925 reference material Substances 0.000 claims description 6
- 230000008859 change Effects 0.000 claims description 3
- 238000004590 computer program Methods 0.000 claims description 3
- 230000008569 process Effects 0.000 abstract description 16
- 239000003814 drug Substances 0.000 abstract description 8
- 230000000694 effects Effects 0.000 abstract description 7
- 238000012552 review Methods 0.000 abstract description 7
- 229940079593 drug Drugs 0.000 abstract description 4
- 238000010561 standard procedure Methods 0.000 description 22
- 238000012549 training Methods 0.000 description 9
- 238000013519 translation Methods 0.000 description 9
- 238000004891 communication Methods 0.000 description 4
- 238000010586 diagram Methods 0.000 description 4
- 238000012986 modification Methods 0.000 description 4
- 230000004048 modification Effects 0.000 description 4
- 230000008878 coupling Effects 0.000 description 3
- 238000010168 coupling process Methods 0.000 description 3
- 238000005859 coupling reaction Methods 0.000 description 3
- 230000006870 function Effects 0.000 description 3
- 238000004364 calculation method Methods 0.000 description 2
- 206010003591 Ataxia Diseases 0.000 description 1
- 206010010947 Coordination abnormal Diseases 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 238000004422 calculation algorithm Methods 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 238000013461 design Methods 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 238000001647 drug administration Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 230000036541 health Effects 0.000 description 1
- 238000007689 inspection Methods 0.000 description 1
- 210000001503 joint Anatomy 0.000 description 1
- 208000028756 lack of coordination Diseases 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 230000008520 organization Effects 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 230000001915 proofreading effect Effects 0.000 description 1
- 238000003908 quality control method Methods 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 230000001502 supplementing effect Effects 0.000 description 1
Images
Classifications
-
- G—PHYSICS
- G06—COMPUTING; CALCULATING OR COUNTING
- G06F—ELECTRIC DIGITAL DATA PROCESSING
- G06F40/00—Handling natural language data
- G06F40/10—Text processing
- G06F40/166—Editing, e.g. inserting or deleting
- G06F40/186—Templates
-
- G—PHYSICS
- G16—INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR SPECIFIC APPLICATION FIELDS
- G16H—HEALTHCARE INFORMATICS, i.e. INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR THE HANDLING OR PROCESSING OF MEDICAL OR HEALTHCARE DATA
- G16H15/00—ICT specially adapted for medical reports, e.g. generation or transmission thereof
-
- G—PHYSICS
- G16—INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR SPECIFIC APPLICATION FIELDS
- G16H—HEALTHCARE INFORMATICS, i.e. INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR THE HANDLING OR PROCESSING OF MEDICAL OR HEALTHCARE DATA
- G16H40/00—ICT specially adapted for the management or administration of healthcare resources or facilities; ICT specially adapted for the management or operation of medical equipment or devices
- G16H40/20—ICT specially adapted for the management or administration of healthcare resources or facilities; ICT specially adapted for the management or operation of medical equipment or devices for the management or administration of healthcare resources or facilities, e.g. managing hospital staff or surgery rooms
Abstract
The invention relates to the technical field of medicines, in particular to a method for generating a medicine document, which comprises the steps of obtaining an editing instruction, and generating an original structural document according to a preset template, wherein the preset template comprises a main content module; the original structural document is generated, stored to a preset path and shared; setting a user group, and giving the members in the user group the operation authority to the original structural document; receiving an operation instruction of a member of a user group on the original structural document, and generating operation information on an interface of the original structural document; and generating a manuscript document according to the original structural document and the operation information. By integrating different users, the original structural document is shared, reviewed and commented, and the like, so that the technical problems of insufficient receiving and sending asynchronism, insufficient review coordination and the like in the traditional medical document generation process are solved, and the technical effects of improving the document generation efficiency and the document generation quality are achieved.
Description
Technical Field
The invention relates to the technical field of medicines, in particular to a method, equipment and a storage medium for generating a medicine document.
Background
With the development of the pharmaceutical industry, the importance of process management in the subdivided fields of health, medicines, medical instruments and the like is more and more prominent, and as the pharmaceutical industry has special requirements on the professional properties of personnel, many enterprises are often difficult to build a process management architecture. The medical documents are the whole process of guiding the quality center and the related business departments to establish, maintain, update and abolish the standard operation flow files, and ensure that the management of the standard operation flow files by the company meets the management system, the flow and the related requirements of the company.
In the prior art, the generation of the medical document is implemented by annotating or modifying the medical document by roles with different responsibilities in modes of chatting groups, mails and the like, and the generation efficiency and the quality of the medical document are low and poor due to the asynchronism of receiving and sending and the lack of coordination between review.
Accordingly, the present invention is directed to such a system.
Disclosure of Invention
The present invention is directed to a method, an apparatus, and a storage medium for generating a medical document, so as to solve at least one of the above technical problems.
The invention provides a method for generating a medical document, which comprises the following steps:
acquiring an editing instruction, and generating an original structural document according to a preset template, wherein the preset template comprises a main content module; the original structural document is generated, stored to a preset path and shared; setting a user group, and giving the members in the user group the operation authority to the original structural document; receiving an operation instruction of a member of a user group on the original structural document, and generating operation information on an interface of the original structural document; and generating a manuscript document according to the original structural document and the operation information.
Further, the step of obtaining an editing instruction and generating an original structural document according to a preset template includes:
the preset template also comprises a reference material module; generating an editing mode corresponding to the main content module according to the main content module; calling a database; identifying whether a subfield consistent with a preset field in a data bank exists in the main content field generated by the editing mode; if so, marking the subfield as a target field, and generating a mapping relation between the target field and a preset field; generating corresponding preset fields and preset field extension information in the reference data module according to the mapping relation; and generating an original structural document according to the main content module and the reference material module.
Further, the step of identifying whether a sub-field consistent with a preset field in a data bank exists in the main content field generated by the editing mode, and if yes, marking the sub-field as a target field comprises:
identifying a subfield class; acquiring a field threshold corresponding to the subfield type; and comparing the sub-fields meeting the field threshold condition with a preset field, and marking the sub-fields with consistent comparison results as target fields.
Preferably, the step of comparing the sub-fields meeting the field threshold condition with a preset field, and marking the sub-fields with consistent comparison results as target fields comprises:
and comparing whether the sub-fields are the same as the preset fields or not, and marking the sub-fields with the same comparison result as target fields.
Further, the step of marking the subfields with the same comparison result as the target field further comprises:
obtaining a difference threshold value for measuring the difference degree between the subfield and the preset field; identifying and extracting different subfields from the comparison result, and calculating the difference between the subfields and a preset field; marking the subfield as a target field on a condition that the disparity satisfies a disparity threshold.
Preferably, the step further comprises after the condition that the degree of difference satisfies the degree of difference threshold: and displaying the target fields in a distinguishing way.
Further, the step of giving the operation right of the original structural document to the members in the user group comprises:
the preset template comprises a user setting module; and acquiring and giving the members in the user group the operation authority to the original structural document according to the user attributes in the user setting module and the preset operation range mapping rule.
Further, before the step of generating the finalized document, the method includes:
receiving an operation instruction of a member of a user group on the original structural document, and generating an intermediate document; identifying whether there is a change in data in each module and/or repository of the intermediate document; and sending a message prompt to the user group if the judgment is yes.
The invention also protects equipment based on the medical document generation method, which comprises a memory, a processor and a computer program stored on the memory and capable of running on the processor, wherein the processor realizes the method when executing the program.
The invention also protects a storage medium based on a method of generating a medical document, the storage medium comprising one or more programs executable by a processor to perform the method described above.
In conclusion, the invention has the following beneficial effects:
1. by integrating different users and sharing the original structural document, the technical problems of insufficient receiving and sending asynchronism, insufficient consistency between review and the like in the traditional medical document generation process are solved, and the technical effects of improving the document generation efficiency and the document generation quality are achieved.
2. The sub-fields and the preset fields are marked to mark the target fields, and then the corresponding preset fields and the preset field extension information are generated in the reference data module, so that the technical problem that terms, rules and the like in document editing cannot be timely and accurately consulted when a user reviews, annotates or modifies the documents is solved, and the technical effects of improving the document generation efficiency and the document generation quality are achieved.
3. The technical problem that field noise is too large in a preset field in a reference data module is solved by setting the field threshold, and the technical effect of improving the reference efficiency is achieved.
Drawings
In order to more clearly illustrate the embodiments of the present invention or the technical solutions in the prior art, the drawings used in the description of the embodiments or the prior art will be briefly described below, it is obvious that the drawings in the following description are only some embodiments of the present invention, and for those skilled in the art, other drawings can be obtained according to the drawings without creative efforts.
FIG. 1 is a flow chart of one embodiment of the present invention;
FIG. 2 is a flow diagram of generating an original structural document in one embodiment of the invention;
FIG. 3 is a schematic diagram of a reference module according to an embodiment of the present invention;
FIG. 4 is a schematic diagram of another embodiment of a reference module according to the present invention;
FIG. 5 is a flow diagram of marking a target field in one embodiment of the present invention;
FIG. 6 is a flow chart of marking a target field in yet another embodiment of the present invention.
Detailed Description
Reference will now be made in detail to the exemplary embodiments, examples of which are illustrated in the accompanying drawings. When the following description refers to the accompanying drawings, like numbers in different drawings represent the same or similar elements unless otherwise indicated. The embodiments described in the following exemplary embodiments do not represent all embodiments consistent with the present invention. Rather, they are merely examples of apparatus and methods consistent with certain aspects of the invention, as detailed in the appended claims.
The terminology used herein is for the purpose of describing particular embodiments only and is not intended to be limiting of the invention. As used in this specification and the appended claims, the singular forms "a", "an", and "the" are intended to include the plural forms as well, unless the context clearly indicates otherwise. It should also be understood that the term "and/or" as used herein refers to and encompasses any and all possible combinations of one or more of the associated listed items.
Referring to fig. 1, the method for generating a medical document according to the present invention includes the steps of:
s100: acquiring an editing instruction, and generating an original structural document according to a preset template, wherein the preset template comprises a main content module;
s200: the original structural document is generated, stored to a preset path and shared;
s300: setting a user group, and giving the members in the user group the operation authority to the original structural document;
s400: and receiving an operation instruction of the members of the user group on the original structural document, and generating a finalized document.
By adopting the scheme, the medical document can be used for the whole process of establishing, maintaining, updating and abolishing a Standard Operating Procedure (SOP) file by each department of a medical company, ensures that the management of the SOP file by the company meets the Requirements of the SOP, ICH-GCP (Good Clinical Practice, quality management Standard of medicine Clinical trials) and globally or locally Applicable medical regulations (Applicable Regulatory Requirements) of the company, and can also be suitable for other document template formats. In the generation of the medical document, the user group may include roles of document managers, coordinators, reviewers, approvers, training system dockers, and trainees, in addition to editors.
The editing instruction in step S100 is sent by the editor, and the original structural document may be uploaded to the shared platform so that other roles in the user group may also be viewed, for example, platform login may be performed in a login manner such as a web page and an APP. The operation authority can be endowed according to different role responsibilities in the user group. For example, the editor's duties may be processes of drafting, coordinating review, finalization, signing, publishing, training, validating, and archiving of SOP documents; the responsibility of the document administrator can be to assign SOP numbers and version numbers, quality control inspection before SOP finalization, centralized management of SOP files and attachments, to ensure that SOP or attached form files that have been invalidated and discarded are withdrawn from all SOP publishing and training systems; the responsibility of the coordinator can be assigned to the quality management personnel by the quality center responsible person to play a role in coordinating and following the whole SOP life cycle management process of starting or updating, reviewing, examining and approving, abolishing, publishing, training, taking effect, archiving and the like of the SOP; the reviewer can be served by the SME (Subject Matter Expert Business area Expert) in the related field, and is responsible for participating in the review of the SOP and providing review opinions; the approver is responsible for auditing and confirming the SOP of the finalized draft, and signing and approving the SOP final draft according to the SOP file and corresponding requirements; the training system butt joint person can confirm and distribute the training courses of the issued SOPs, confirm and update or abolish the training courses of the related SOPs, and issue and maintain SOP file searching system functions, including SOP lookup and work file downloading; the trainees can complete the SOP learning or training in time according to the requirement of the SOP release information.
The main content module may include a flow module, an application range module, a writing destination module, and the like, and different main content modules and formats may be generated according to different template types in table 1.
TABLE 1
The operation instruction may be made by one or more roles in the user group, for example, if the reviewer or the approver makes an adjustment suggestion for the process part in the original structural document, the composer may make a corresponding operation instruction according to the adjustment suggestion, the corresponding operation instruction may be an instruction for directly modifying the original structural document or a reply instruction for the adjustment suggestion, and each user may view the original structural document after logging in its account.
By integrating different users, the technical problems that in the traditional medical document generation process, multiple parties need to be dispersed and coordinated, the latest document information cannot be obtained in real time, the document generation speed is low, information asymmetry is easy to occur among different users and the like are solved, and the technical effects of improving the document generation efficiency and the document generation quality are achieved.
Referring to fig. 2, 3 and 4, the step of obtaining an editing instruction and generating an original structural document according to a preset template includes:
s101: the preset template also comprises a reference material module;
s102: generating an editing mode corresponding to the main content module according to the main content module;
s103: calling a database;
s104: identifying whether a subfield consistent with a preset field in a data bank exists in the main content field generated by the editing mode;
s105: if so, marking the subfield as a target field, and generating a mapping relation between the target field and a preset field;
s106: generating corresponding preset fields and preset field extension information in the reference data module according to the mapping relation;
s107: and generating an original structural document according to the main content module and the reference material module.
With the above solution, the reference module may include a reference module, a term or abbreviation module, an attachment module, etc., the reference module may be used to generate information associated with regulations, such as drug administration law, quality management specifications of clinical trials of drugs, etc., and the term or abbreviation module may be used to generate information related to medical professional terms. The editing mode can be directly generated by calling the underlying statement or a freely written typing mode. The database comprises a rule library, a term library, a abbreviation library and the like. The main content module can comprise modules of making user roles, supplementing information, dividing and describing functions, main flow and the like, when a user composes the modules, the input content generally relates to relevant laws and regulations, special terms, abbreviations and the like, and the relevant laws and regulations generally need to quote specific terms in the relevant laws and regulations, wherein the specific terms are required to be inquired by reviewers, approvers, experts and the like in a user group, and in addition, the medical field special terms and abbreviations relate to a plurality of even experts and are difficult to be completely understood; moreover, the editor usually needs to query corresponding laws and regulations, professional terms, abbreviations and the like when editing by himself, and browsing and querying through the internet has many problems, such as technical problems that the versions of laws and regulations are old and cannot be updated timely, some internal laws and regulations are available on the internet in a passive mode, the professional terms and abbreviations are easy to be confused in other fields, and the query efficiency is low. The preset field can be the name of a regulation or a regulation, a professional term or the name of an abbreviation, and the language can support Chinese or foreign language; for identifying the sub-fields in the main content field, a method of cutting words and then identifying the words one by one in a duplication checking technology can be adopted, when the editor identifies the mapping relation between the target field and the preset field in the process of inputting the main field or after the main field is input, the preset field can be generated at the corresponding position in the graph 3 or the graph 4 through the mapping relation, and the preset field extension information can be the issuing organization, the issuing number, the issuing year and month and the like of the laws and regulations.
In some other embodiments of the present invention, the reference data may also be written in a freely editable manner in the reference data module.
Referring to fig. 5, the step of identifying whether a sub-field consistent with a preset field in a data bank exists in the main content field generated by the editing mode, and if yes, marking the sub-field as a target field includes identifying a sub-field type; acquiring a field threshold corresponding to the subfield type; and comparing the sub-fields meeting the field threshold condition with a preset field, and marking the sub-fields with consistent comparison results as target fields.
By adopting the scheme, the field types can comprise Chinese, English and other foreign languages, characters and the like, for example, for a role editing module in a main content module, abbreviations of positions such as English abbreviation PM, MD and the like are usually input, and setting of a field threshold in the role editing module meets the requirement that subfields with more than two English letters are compared with a preset field; for example, a large number of Chinese characters are generally needed for the flow writing part, and the conditions that two Chinese characters are used, such as rules, abbreviations and terms in the Chinese characters, are less, so that the field threshold value can be adjusted upwards, and excessive noise interference is avoided.
Comparing the sub-fields meeting the field threshold condition with a preset field, marking the sub-fields with the consistent comparison result as target fields, and marking the sub-fields with the same comparison result as the target fields.
By adopting the scheme, the comparison result shows that the subfields are the same as the preset field types and the field lengths, for example, if the 'SME' edited in the text of the main content module is the same as the service field Expert (Subject Matter Expert) in the abbreviation library, the 'SME' is marked as the target field, and corresponding English full-name and Chinese full-name information can be generated in the corresponding abbreviation list.
Referring to fig. 6, after marking the subfields with the same comparison result as the target field, the step further includes obtaining a difference threshold for measuring the difference between the subfields and the preset field; identifying and extracting different subfields from the comparison result, and calculating the difference between the subfields and a preset field; marking the subfield as a target field on a condition that the disparity satisfies a disparity threshold.
By adopting the scheme, the situation that the writer wrongly writes partial nouns in laws and regulations, professional terms and abbreviations in the process of writing can occur, and because the writer is a person with a certain medicine knowledge base, the caused writing errors are usually small, such as errors of one Chinese character or one letter and stroke errors. Since the preset fields in the database are standard and error-free, when the comparison result is required to be the same, the editor cannot form a mapping with the preset fields due to negligence or miswritten laws and regulations, professional terms and abbreviations, so that the reviewers, clients and the like cannot find explanations of related nouns during browsing, and further repeated communication is caused, and the document generation efficiency is influenced. The calculation of the difference degree can be used for calculating the condition that the characters of the sub-field are the same as the characters of the preset field but the characters are different from the characters of the sub-field and the condition that the characters of the sub-field are more than or less than the characters of the sub-field, and the preset field similar to the sub-field can be generated through the setting of the difference degree threshold value and the calculation of the difference degree, so that the technical problems of low document generation efficiency and poor quality caused by repeated communication with other users in the following process are solved.
In some other embodiments of the present invention, the step further comprises displaying the target field distinctively after the condition that the degree of difference satisfies a degree of difference threshold.
By adopting the scheme, the differential display can help the editor to identify errors occurring in the writing, so that the quality of medical document generation is improved, and the differential display can adopt the modes of highlight display, color marking and the like.
In some other embodiments of the present invention, the step of giving the operation authority of the members in the user group to the original structural document includes that the preset template includes a user setting module; and acquiring and giving the members in the user group the operation authority to the original structural document according to the user attributes in the user setting module and the preset operation range mapping rule.
By adopting the scheme, the user setting module is used for integrating participants, the participants can be editors, coordinators, reviewers and the like, the user attributes can be roles, positions, fields, departments and the like, the preset operation range mapping rule can be preset, for example, the reviewers and the approvers have the permission to annotate or modify the main content flow part, and the coordinators do not have the permission to modify the main content flow part. The scheme can prevent irrelevant personnel from tampering or falsely modifying the editing content of the specific module, and improves the safety and the document quality in the document generation process.
In some other embodiments of the present invention, before the step of generating the finalized document, the method includes receiving an operation instruction of a member of the user group on the original structural document, and generating an intermediate document; identifying whether there is a change in data in each module and/or repository of the intermediate document; and sending a message prompt to the user group if the judgment is yes.
By adopting the scheme, when the contents in the process and the database are updated or modified, prompts such as a dialog box or a dynamic flashing icon can be generated on a login interface of a user, so that the user can quickly know the dynamic state in the document generation process, and the technical effect of improving the document generation efficiency is achieved.
In some other embodiments of the present invention, the step of generating the finalized document according to the original structural document and the operation information further includes recognizing a current document editing language, translating the current document editing language into another language, such as english, french, german, and the like, and a translation proofreading person may be further introduced into the user group, and may perform annotation, marking, and the like on the translation text after logging in an account number to check the machine translation text. The translation proofreader can be provided with a plurality of translation proofreaders, the document interface can display opinions of the translation proofreaders on the same interface, and when different opinions appear, the translation proofreaders can communicate with each other in a remark mode to determine the final translation text. The scheme provides a mode of generating the medical document content into multiple languages, and translation accuracy is improved.
In some other embodiments of the present invention, the medical document may be generated into a format such as Word or PPt by file format conversion, for example, different parts may be divided to match different needs, and the scheme may be conveniently used for training or circulation.
The invention also protects equipment based on the medical document generation method, which comprises a memory, a processor and a computer program stored on the memory and capable of running on the processor, wherein the processor realizes the method when executing the program.
The invention also protects a storage medium based on a method of generating a medical document, the storage medium comprising one or more programs executable by a processor to perform the method described above.
It should be noted that, for those skilled in the art, it is possible to make several improvements and modifications to the present invention without departing from the principle of the present invention, and those improvements and modifications also fall within the protection scope of the claims of the present invention.
Those of ordinary skill in the art will appreciate that the various illustrative elements and algorithm steps described in connection with the embodiments disclosed herein may be implemented as electronic hardware or combinations of computer software and electronic hardware. Whether such functionality is implemented as hardware or software depends upon the particular application and design constraints imposed on the implementation. Skilled artisans may implement the described functionality in varying ways for each particular application, but such implementation decisions should not be interpreted as causing a departure from the scope of the present invention.
In the several embodiments provided in the present application, it should be understood that the disclosed system, apparatus and method may be implemented in other ways. In addition, the shown or discussed mutual coupling or direct coupling or communication connection may be an indirect coupling or communication connection through some interfaces, devices or units, and may be in an electrical, mechanical or other form.
The units described as separate parts may or may not be physically separate, and parts displayed as units may or may not be physical units, may be located in one place, or may be distributed on a plurality of network units. Some or all of the units can be selected according to actual needs to achieve the purpose of the solution of the embodiment.
In addition, functional units in the embodiments of the present invention may be integrated into one processing unit, or each unit may exist alone physically, or two or more units are integrated into one unit.
It should be understood that the technical problems can be solved by combining and combining the features of the embodiments from the claims.
The functions, if implemented in the form of software functional units and sold or used as a stand-alone product, may be stored in a computer readable storage medium. Based on such understanding, the technical solution of the present invention may be embodied in the form of a software product, which is stored in a storage medium and includes instructions for causing a computer device (which may be a personal computer, a server, or a network device) to execute all or part of the steps of the method according to the embodiments of the present invention. And the aforementioned storage medium includes: a U-disk, a removable hard disk, a Read-Only Memory (ROM), a Random Access Memory (RAM), a magnetic disk or an optical disk, and other various media capable of storing program codes.
The previous description of the disclosed embodiments is provided to enable any person skilled in the art to make or use the present invention. Various modifications to these embodiments will be readily apparent to those skilled in the art, and the generic principles defined herein may be applied to other embodiments without departing from the spirit or scope of the invention. Thus, the present invention is not intended to be limited to the embodiments shown herein but is to be accorded the widest scope consistent with the principles and novel features disclosed herein, the foregoing description of the disclosed embodiments being directed to enabling one skilled in the art to make and use the present invention. Various modifications to these embodiments will be readily apparent to those skilled in the art, and the generic principles defined herein may be applied to other embodiments without departing from the spirit or scope of the invention. Thus, the present invention is not intended to be limited to the embodiments shown herein but is to be accorded the widest scope consistent with the principles and novel features disclosed herein.
Claims (10)
1. A method for generating a medical document, comprising the steps of:
acquiring an editing instruction, and generating an original structural document according to a preset template, wherein the preset template comprises a main content module;
the original structural document is generated, stored to a preset path and shared;
setting a user group, and giving the members in the user group the operation authority to the original structural document;
receiving an operation instruction of a member of a user group on the original structural document, and generating operation information on an interface of the original structural document;
and generating a manuscript document according to the original structural document and the operation information.
2. The method of claim 1, wherein the step of obtaining an editing instruction and generating the original structural document according to the preset template comprises:
the preset template also comprises a reference material module;
generating an editing mode corresponding to the main content module according to the main content module;
calling a database;
identifying whether a subfield consistent with a preset field in a data bank exists in the main content field generated by the editing mode;
if so, marking the subfield as a target field, and generating a mapping relation between the target field and a preset field;
generating corresponding preset fields and preset field extension information in the reference data module according to the mapping relation;
and generating an original structural document according to the main content module and the reference material module.
3. The method of claim 2, wherein the step of identifying whether a sub-field consistent with a preset field in the data bank exists in the main content field generated by the editing mode comprises the following steps:
identifying a subfield class;
acquiring a field threshold corresponding to the subfield type;
and comparing the sub-fields meeting the field threshold condition with a preset field, and marking the sub-fields with consistent comparison results as target fields.
4. The method of claim 3, wherein the step of comparing the sub-fields meeting the field threshold condition with a preset field, and the step of marking the sub-fields with consistent comparison results as target fields comprises:
and comparing whether the sub-fields are the same as the preset fields or not, and marking the sub-fields with the same comparison result as target fields.
5. The method of generating a medical document according to claim 4, wherein the step of marking the subfields with the same comparison result as the target field further comprises:
obtaining a difference threshold value for measuring the difference degree between the subfield and the preset field;
identifying and extracting different subfields from the comparison result, and calculating the difference between the subfields and a preset field;
marking the subfield as a target field on a condition that the disparity satisfies a disparity threshold.
6. The method for generating a medical document according to claim 5, further comprising, after the step of generating the medical document, the step of: and displaying the target fields in a distinguishing way.
7. A method for generating a medical document according to any one of claims 1-6, wherein the step of giving the members of the user group the operation right to the original structural document comprises:
the preset template comprises a user setting module;
obtaining and mapping rules according to the user attributes and the preset operation range in the user setting module,
and giving the members in the user group the operation authority to the original structural document.
8. The method for generating a medical document according to any one of claims 1 to 6, wherein the step of generating a finalized document includes:
receiving an operation instruction of a member of a user group on the original structural document, and generating an intermediate document;
identifying whether there is a change in data in each module and/or repository of the intermediate document;
and sending a message prompt to the user group if the judgment is yes.
9. An apparatus based on a generation method of a medical document, characterized by comprising: memory, processor and computer program stored on the memory and executable on the processor, which when executed by the processor implements the method of any of the preceding claims 1 to 8.
10. A storage medium based on a generation method of a medical document, characterized in that: the storage medium includes one or more programs that are executable by a processor to perform the method of any of claims 1-8.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN202110690182.XA CN113392626A (en) | 2021-06-22 | 2021-06-22 | Method and device for generating medical document and storage medium |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN202110690182.XA CN113392626A (en) | 2021-06-22 | 2021-06-22 | Method and device for generating medical document and storage medium |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CN113392626A true CN113392626A (en) | 2021-09-14 |
Family
ID=77623306
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN202110690182.XA Pending CN113392626A (en) | 2021-06-22 | 2021-06-22 | Method and device for generating medical document and storage medium |
Country Status (1)
| Country | Link |
|---|---|
| CN (1) | CN113392626A (en) |
Citations (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN106095771A (en) * | 2016-05-07 | 2016-11-09 | 深圳职业技术学院 | Writing householder method and device |
| CN106844318A (en) * | 2016-12-20 | 2017-06-13 | 北京华宇信息技术有限公司 | Document intelligence write method, document intelligently write device and computer-readable storage medium |
| CN109597976A (en) * | 2018-10-11 | 2019-04-09 | 阿里巴巴集团控股有限公司 | A kind of document edit method and device |
| CN109800303A (en) * | 2018-12-28 | 2019-05-24 | 深圳市世强元件网络有限公司 | A kind of document information extracting method, storage medium and terminal |
| CN110956029A (en) * | 2019-12-19 | 2020-04-03 | 青岛知识谷云科技有限公司 | Technical document processing method and system |
| CN112765948A (en) * | 2020-12-31 | 2021-05-07 | 山西三友和智慧信息技术股份有限公司 | Document generation editing method |
-
2021
- 2021-06-22 CN CN202110690182.XA patent/CN113392626A/en active Pending
Patent Citations (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN106095771A (en) * | 2016-05-07 | 2016-11-09 | 深圳职业技术学院 | Writing householder method and device |
| CN106844318A (en) * | 2016-12-20 | 2017-06-13 | 北京华宇信息技术有限公司 | Document intelligence write method, document intelligently write device and computer-readable storage medium |
| CN109597976A (en) * | 2018-10-11 | 2019-04-09 | 阿里巴巴集团控股有限公司 | A kind of document edit method and device |
| CN109800303A (en) * | 2018-12-28 | 2019-05-24 | 深圳市世强元件网络有限公司 | A kind of document information extracting method, storage medium and terminal |
| CN110956029A (en) * | 2019-12-19 | 2020-04-03 | 青岛知识谷云科技有限公司 | Technical document processing method and system |
| CN112765948A (en) * | 2020-12-31 | 2021-05-07 | 山西三友和智慧信息技术股份有限公司 | Document generation editing method |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US11210456B2 (en) | Method relating to preparation of a report | |
| US20230105237A1 (en) | Document processor program having document-type dependent user interface | |
| US7725499B1 (en) | Semantic architecture for managing information through structured storage and retrieval | |
| US20130238987A1 (en) | Patent Prosecution Tool | |
| US20080155411A1 (en) | Method for ensuring internet content compliance | |
| Sommerville | Software documentation | |
| Haaf et al. | The dta “base format”: A tei subset for the compilation of a large reference corpus of printed text from multiple sources | |
| EA012691B1 (en) | An automated publishing system that facilitates collaborative editing and accountability through virtual document architecture | |
| Kugler et al. | Translator’s workbench: Tools and terminology for translation and text processing | |
| US20140115433A1 (en) | Business management system and method | |
| Hurrell et al. | Implementation of a standards-based anaesthesia record compliant with the health level 7 (HL7) clinical document architecture (CDA) | |
| Frase | Human factors and behavioral science: The UNIX™ Writer'S workbench software: Philosophy | |
| Haaf et al. | Enabling the Encoding of Manuscripts within the DTABf: Extension and Modularization of the Format | |
| CN113392626A (en) | Method and device for generating medical document and storage medium | |
| CN111753513A (en) | Electronic contract making method based on HTML language | |
| Nash | Spreadsheets in statistical practice—another look | |
| Adhya | Key elements of an effective style guide in the new age | |
| Anastasiou et al. | Localisation standards and metadata | |
| He | Developing and validating a revision scheme to account for both source and target texts: The case of Japanese to Chinese translation of hybrid texts | |
| Majewski | Design and implementation of a research infrastructure for a corpus of spoken ELF | |
| Dong et al. | Translation, Localization, or Creation? The Stories Behind Developing Style Guides for Chinese Technical Documents | |
| McCay et al. | Results of investigating the transformability between HL7 V3, openEHR and EN/ISO 13606 | |
| Hughes et al. | Conquering APA Style for the Seventh Edition: Advice From APA Style Experts. | |
| Headquarters | TYPES OF PAPERS | |
| Lorenzo | Using XML Schema with Embedded Schematron Rules for MODS Quality Control in a Digital Repository |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PB01 | Publication | ||
| PB01 | Publication | ||
| SE01 | Entry into force of request for substantive examination | ||
| SE01 | Entry into force of request for substantive examination |