CN117238435A - Prescription auditing method, device and equipment - Google Patents
Prescription auditing method, device and equipment Download PDFInfo
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- 238000000034 method Methods 0.000 title claims abstract description 53
- 238000012550 audit Methods 0.000 claims abstract description 179
- 239000003814 drug Substances 0.000 claims description 214
- 229940079593 drug Drugs 0.000 claims description 101
- 238000012797 qualification Methods 0.000 claims description 43
- 238000003745 diagnosis Methods 0.000 claims description 38
- 201000010099 disease Diseases 0.000 claims description 32
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims description 32
- 208000024891 symptom Diseases 0.000 claims description 10
- 206010067484 Adverse reaction Diseases 0.000 claims description 9
- 230000006838 adverse reaction Effects 0.000 claims description 9
- 238000004590 computer program Methods 0.000 claims description 8
- 238000012552 review Methods 0.000 description 23
- 238000012986 modification Methods 0.000 description 6
- 230000004048 modification Effects 0.000 description 6
- 238000007726 management method Methods 0.000 description 5
- 238000004891 communication Methods 0.000 description 4
- 238000010586 diagram Methods 0.000 description 2
- 230000036541 health Effects 0.000 description 2
- 238000004458 analytical method Methods 0.000 description 1
- 238000012790 confirmation Methods 0.000 description 1
- 238000012217 deletion Methods 0.000 description 1
- 230000037430 deletion Effects 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 230000003203 everyday effect Effects 0.000 description 1
- 230000010365 information processing Effects 0.000 description 1
- 238000007689 inspection Methods 0.000 description 1
- 230000003993 interaction Effects 0.000 description 1
- 229940126532 prescription medicine Drugs 0.000 description 1
- 230000008569 process Effects 0.000 description 1
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02A—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE
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Abstract
The application discloses a prescription auditing method, device and equipment, relates to the technical field of digital medical treatment, and can solve the technical problems of low manual auditing efficiency, easiness in error and high cost. The method comprises the following steps: acquiring a current prescription to be checked; obtaining an auditing template of the current prescription to be audited, wherein the auditing template is constructed in advance based on auditing items, auditing rules and specification data; and utilizing the auditing template to audit the current prescription to be audited to obtain a template auditing result.
Description
Technical Field
The present application relates to the field of digital medical technology, and in particular, to a method, an apparatus, and a device for checking prescriptions.
Background
At present, doctor auditing systems and pharmacist auditing systems in companies manually process complex auditing flows, some auditing flows of auditing sheets are longer, and auditing sheets are detained in peak periods, so that users cannot purchase prescription medicines in time, the auditing efficiency is low, manual auditing is easy to make mistakes, and the labor cost is high.
Disclosure of Invention
In view of the above, the application provides a prescription auditing method, device and equipment, which can solve the technical problems of low manual auditing efficiency, easy error and high cost.
According to a first aspect of the present application, there is provided a prescription auditing method, the method comprising:
acquiring a current prescription to be checked;
obtaining an auditing template of the current prescription to be audited, wherein the auditing template is constructed in advance based on auditing items, auditing rules and specification data;
and utilizing the auditing template to audit the current prescription to be audited to obtain a template auditing result.
Preferably, the obtaining an audit template of the prescription to be audited currently includes:
identifying whether the current prescription to be checked has a package prescription identification;
if the package prescription mark is not provided, a medicine auditing template, a medication prescribing qualification auditing template and a diagnosis auditing template are obtained, wherein the auditing items included in the medicine auditing template are applicable crowd auditing items, usage quantity auditing items and tabu medicine auditing items, the auditing items included in the medication prescribing qualification auditing template are medication prescribing qualification and medicine risk matching degree auditing items, and the auditing items included in the diagnosis auditing template are medicine applicable disease auditing items and basic disease aggravating auditing items caused by medicine adverse reactions;
the method for auditing the currently-to-be-audited prescription by utilizing the auditing template comprises the following steps:
and checking the current prescription to be checked by using the medicine checking template, the medication prescribing qualification checking template and the diagnosis checking template.
Preferably, the method further comprises:
if the package prescription identification exists, obtaining a package auditing template of the current prescription to be audited, wherein the package auditing template comprises a package medicine set;
the method for auditing the currently-to-be-audited prescription by utilizing the auditing template comprises the following steps:
extracting a to-be-checked medicine set of the current to-be-checked prescription;
checking whether the drug set to be checked is the same as the package drug set;
and if the current prescription to be audited is the same, utilizing the medicine audit template, the medication prescribing qualification audit template and the diagnosis audit template to audit the current prescription to be audited.
Preferably, the method further comprises:
if the template auditing result is that the current prescription to be audited fails the template auditing, the current prescription to be audited and the non-template auditing item are sent to a manual auditing terminal;
and receiving a manual auditing result fed back by the manual auditing terminal.
Preferably, the method further comprises:
if the manual auditing result is that the current prescription to be audited does not pass the manual auditing, the current prescription to be audited and the non-passing manual auditing item are sent to a terminal of a drug issuer;
receiving an updated prescription to be checked fed back by the terminal of the prescriber;
and auditing the updated prescription to be audited by utilizing the auditing template to obtain an auditing result of the updated template.
Preferably, before the obtaining of the audit template of the currently pending prescription, the method further includes:
receiving configuration of auditing items and corresponding auditing rules;
extracting specification data corresponding to each drug and each type of auditing item from a drug information base;
and generating the auditing template according to each type of auditing item, the corresponding auditing rule and the specification data.
Preferably, before the obtaining the currently pending prescription, the method further includes:
configuring a prescription template, wherein the prescription template comprises: the system comprises a prescriber qualification field, a prescriber field, a diagnosis field, a medication field and a package prescription mark, wherein the prescriber field comprises a prescriber group field, a prescriber basic disease field and a prescriber basic medication field, the diagnosis field comprises a disease name field, a symptom field and a disease degree field, and the medication field comprises a medicine name field, a medicine usage amount field and a medicine risk field;
and responding to the acquisition request and the information filling request of the prescription template to obtain the currently pending prescription.
According to a second aspect of the present application, there is provided a prescription auditing apparatus, the apparatus comprising:
the first acquisition module is used for acquiring a current prescription to be checked;
the second acquisition module is used for acquiring an audit template of the current prescription to be audited, wherein the audit template is constructed in advance based on audit items, audit rules and specification data;
and the template auditing module is used for auditing the current prescription to be audited by utilizing the auditing template to obtain a template auditing result.
Optionally, the second obtaining module 32 may be specifically configured to identify whether the currently pending prescription has a package prescription identifier; if the package prescription mark is not provided, a medicine auditing template, a medication prescribing qualification auditing template and a diagnosis auditing template are obtained, wherein the auditing items included in the medicine auditing template are applicable crowd auditing items, usage quantity auditing items and tabu medicine auditing items, the auditing items included in the medication prescribing qualification auditing template are medication prescribing qualification and medicine risk matching degree auditing items, and the auditing items included in the diagnosis auditing template are medicine applicable disease auditing items and basic disease aggravating auditing items caused by medicine adverse reactions.
Optionally, the template auditing module 33 may be specifically configured to audit the prescription to be audited currently by using the drug auditing template, the medication prescribing qualification auditing template, and the diagnostic auditing template.
Optionally, the second obtaining module 32 may be specifically further configured to obtain a package review template of the currently pending prescription if the package prescription identifier is provided, where the package review template includes a package drug set.
Optionally, the template auditing module 33 may be specifically further configured to extract a set of to-be-inspected medicines of the currently to-be-inspected prescription; checking whether the drug set to be checked is the same as the package drug set; and if the current prescription to be audited is the same, utilizing the medicine audit template, the medication prescribing qualification audit template and the diagnosis audit template to audit the current prescription to be audited.
Optionally, a prescription auditing apparatus, the apparatus further comprises: the manual review module 34 is specifically configured to send the current prescription to be reviewed and the non-passing template review item to a manual review terminal if the template review result indicates that the current prescription to be reviewed does not pass the template review; and receiving a manual auditing result fed back by the manual auditing terminal.
Optionally, a prescription auditing apparatus, the apparatus further comprises: the updating module 35 is specifically configured to send the current prescription to be checked and the non-passing manual checking item to a terminal of a drug issuer if the manual checking result indicates that the current prescription to be checked does not pass the manual checking; receiving an updated prescription to be checked fed back by the terminal of the prescriber; and auditing the updated prescription to be audited by utilizing the auditing template to obtain an auditing result of the updated template.
Optionally, a prescription auditing apparatus, the apparatus further comprises: the generating module 36 is specifically configured to receive a configuration of the audit item and the corresponding audit rule; extracting specification data corresponding to each drug and each type of auditing item from a drug information base; and generating the auditing template according to each type of auditing item, the corresponding auditing rule and the specification data.
Optionally, a prescription auditing apparatus, the apparatus further comprises: the configuration module 37 is specifically configured to configure a prescription template, where the prescription template includes: the system comprises a prescriber qualification field, a prescriber field, a diagnosis field, a medication field and a package prescription mark, wherein the prescriber field comprises a prescriber group field, a prescriber basic disease field and a prescriber basic medication field, the diagnosis field comprises a disease name field, a symptom field and a disease degree field, and the medication field comprises a medicine name field, a medicine usage amount field and a medicine risk field; and responding to the acquisition request and the information filling request of the prescription template to obtain the currently pending prescription.
According to a third aspect of the present application, there is provided a storage medium having stored thereon a computer program which, when executed by a processor, implements the prescription auditing method described above.
According to a fourth aspect of the present application, there is provided a computer device comprising a storage medium, a processor and a computer program stored on the storage medium and executable on the processor, the processor implementing the prescription auditing method described above when executing the program.
By means of the technical scheme, the prescription auditing method, device and equipment provided by the application can firstly acquire the current prescription to be audited; further acquiring an auditing template of the current prescription to be audited, wherein the auditing template is constructed in advance based on auditing items, auditing rules and specification data; finally, the current prescription to be checked is checked by using the checking template, and a template checking result is obtained. According to the technical scheme, the current prescription to be checked is automatically checked according to the pre-constructed checking template, manual checking is not needed, checking efficiency is high, accuracy is high, and cost is low.
The foregoing description is only an overview of the present application, and is intended to be implemented in accordance with the teachings of the present application in order that the same may be more clearly understood and to make the same and other objects, features and advantages of the present application more readily apparent.
Drawings
The accompanying drawings, which are included to provide a further understanding of the application and are incorporated in and constitute a part of this specification, illustrate embodiments of the application and together with the description serve to explain the application and do not constitute an undue limitation to the present application. In the drawings:
FIG. 1 shows a schematic flow chart of a prescription auditing method according to an embodiment of the present application;
FIG. 2 is a flow chart of another method for checking prescriptions according to an embodiment of the present application;
FIG. 3 is a schematic diagram of a prescription auditing apparatus according to an embodiment of the present application;
fig. 4 is a schematic structural diagram of another prescription auditing apparatus according to an embodiment of the present application.
Detailed Description
The application will be described in detail hereinafter with reference to the drawings in conjunction with embodiments. It should be noted that, without conflict, the embodiments of the present application and features of the embodiments may be combined with each other.
The present embodiment provides a prescription auditing method, as shown in fig. 1, including:
101. and obtaining the current prescription to be checked.
In a specific medical scenario, a doctor can prescribe a large number of medicines every day, and due to individual differences of each patient, the medicine types are so great that the medicine schemes in the prescriptions prescribed by the doctor are not necessarily completely reasonable. That is, the current prescription has an unreasonable medication scheme, for example, the unreasonable medication scheme, the corresponding medication management system of the health department, the existing medical insurance policy, etc. are violated, and the unreasonable prescription will have serious influence on the physical health of the patient and increase the medical cost, and it is difficult for the patient to know in time whether the prescription prescribed by the doctor is reasonable or not when the patient is in medical care. Therefore, it is necessary to audit the prescription prescribed by the doctor.
For the embodiment, the prescription issued by the doctor is the currently-to-be-checked prescription, and the prescription checking method can be applied to a prescription checking system, and the prescription checking system can support checking of batches of the currently-to-be-checked prescriptions, and is not limited herein.
102. And acquiring an auditing template of the current prescription to be audited, wherein the auditing template is constructed in advance based on auditing items, auditing rules and specification data.
103. And utilizing the auditing template to audit the current prescription to be audited to obtain a template auditing result.
The prescriptions comprise medical advice sheets for medical institutions in the disease areas, are written documents for doctors to take medicines for patients, are the basis for medicament personnel to allocate medicines, and have legal, technical and economic responsibilities. Therefore, conventional prescription auditing requires a double confirmation by both the physician and pharmacist. In order to improve the auditing efficiency, for the embodiment, not only automatic auditing is performed through a pre-constructed auditing template, manual auditing is not needed, but also auditing of doctors and pharmacists is fused through the auditing template, and only one auditing node (the doctors and the pharmacists are fused into one auditing node) is needed, and no more nodes are needed to be transferred to for auditing (one auditing node of the doctors and the pharmacist is another auditing node).
For example, step 102, before the obtaining the audit template of the currently pending prescription, further includes: receiving configuration of auditing items and corresponding auditing rules; and constructing an audit template by utilizing the audit item and the corresponding audit rule.
The configuration of receiving the audit item and the corresponding audit rule may be that the first audit item and the corresponding first audit rule from the doctor terminal are added, the second audit item and the corresponding second audit rule from the pharmacist terminal are added, then the first audit item and the second audit item are combined to form an audit item, and the first audit rule and the second audit rule are combined to form an audit rule. Preferably, the method further comprises modification of the audit item and/or audit rule, and deletion of the audit item and audit rule, which is not limited herein.
In one embodiment, when the audit template is constructed by using the audit items and the corresponding audit rules, an audit template may be constructed by using a type of audit items and the corresponding audit rules, for example, an audit template may be constructed by using adverse reaction audit items and tabu audit items of a drug as a type of audit items, or an audit template may be constructed by using an audit item and the corresponding audit rules, for example, an audit template may be constructed by using adverse reaction audit items of a drug as an audit item, and a tabu audit item of a drug as an audit item, and a further audit template may be constructed without limitation.
Taking one type of audit item as an example, constructing an audit template, and extracting the standard data corresponding to each type of audit item of each medicine from a medicine information base; and generating the auditing template according to each type of auditing item, the corresponding auditing rule and the specification data.
For example, one audit template includes three audit items (audit item 1, audit item 2, audit item 3) and three audit rules (audit rule 1, audit rule 2, audit rule 3) corresponding to each other, and n drugs, then the audit template includes the following audit items 1, audit rule 1: normative data 11 for drug 1, normative data 12 for drug 2. Under audit item 2, audit rule 2: normative data 21 for drug 1, normative data 22 for drug 2. Under audit item 3, audit rule 3: normative data 31 for drug 1, normative data 32 for drug 2.
The medicine information base comprises the medicine attribute and corresponding medicine standard data, wherein the medicine attribute comprises medicine name, component, function main treatment, usage amount, adverse reaction, tabu, medicine interaction and the like.
For example, in step 102, after the audit template is constructed, the audit templates may be classified according to the prescription type, for example, the prescription type 1 is audited by the audit templates 1, 2, 3, and the audit templates 1, 2, 3 are constructed as audit templates corresponding to the prescription type 1.
Preferably, the auditing order of the auditing templates can also be set according to the prescription type, for example, the prescription type 1 needs auditing of the auditing templates 1, 2 and 3, but if only the auditing results of the auditing templates 1 and 2 are not passed and the auditing template 3 is not needed at this time, the auditing order of the prescription type 1 is set to be firstly audited by using the auditing templates 1 and 2, and whether to audit by using the auditing template 3 is further determined according to the auditing results.
For example step 103, an automatic audit may be implemented and the template audit results include pass and fail.
The prescription auditing method, device and equipment provided by the application can firstly acquire the current prescription to be audited; further acquiring an auditing template of the current prescription to be audited, wherein the auditing template is constructed in advance based on auditing items, auditing rules and specification data; finally, the current prescription to be checked is checked by using the checking template, and a template checking result is obtained. According to the technical scheme, the current prescription to be checked is automatically checked according to the pre-constructed checking template, manual checking is not needed, checking efficiency is high, accuracy is high, and cost is low.
Further, as a refinement and extension of the foregoing embodiment, in order to fully describe the implementation procedure in this embodiment, another prescription auditing method is provided, as shown in fig. 2, and the method includes:
201. and obtaining the current prescription to be checked.
For the present embodiment, the specific implementation is the same as that of embodiment step 101, and will not be described here again.
Preferably, in order to increase the efficiency of the template audit, the fields of the prescription may be unified according to the audit item, i.e. these fields are required by the audit item. Specifically, before the current prescription to be checked is obtained, the method further comprises the following steps: obtaining an audit item (for example, an audit item of applicable people, and knowing that corresponding fields included in a prescription template are the drug group to which a drug belongs according to the audit item); and configuring a prescription template according to the checking item, and responding to an acquisition request and an information filling request of the prescription template to obtain the current prescription to be checked.
Wherein the prescription template comprises: the medicine prescription management system comprises a medicine prescription management system, a medicine prescription management system and a medicine prescription management system, wherein a medicine prescription qualification field, a medicine person field, a diagnosis field, a medicine field and a medicine prescription identification are provided, the medicine person field comprises a medicine crowd field, a medicine person basic disease field and a medicine person basic medicine field, the diagnosis field comprises a disease name field, a symptom field and a disease degree field, and the medicine field comprises a medicine name field, a medicine usage amount field and a medicine risk field.
202. And identifying whether the currently-to-be-checked prescription has a package prescription identification.
Extracting a field value from the current pending prescription having a package prescription identification field to determine whether the current pending prescription has a package prescription identification.
It should be noted that, the pre-constructed audit template includes: the package audit template, the drug audit template, the medication-providing qualification audit template and the diagnosis audit template are taken as examples, and audit sequences among the audit templates are preset, for example, whether the package audit template is used for audit is judged first, if yes, the package audit template is used first, and then the drug audit template, the medication-providing qualification audit template and the diagnosis audit template are utilized for audit, wherein the drug audit template, the medication-providing qualification audit template and the diagnosis audit template have no audit sequence. The method comprises the following steps:
203a, if the package prescription identification is not available, acquiring a medicine auditing template, a medication prescribing qualification auditing template and a diagnosis auditing template.
204a, utilizing the drug auditing template, the prescribing qualification auditing template and the diagnosis auditing template to audit the current prescription to be checked to obtain a template auditing result.
Wherein, the drug auditing template comprises auditing items and auditing rules of { applicable crowd auditing items, whether the drug crowd of the drug person belongs to the standard applicable crowd }, { usage auditing items, whether the usage of the drug under the illness degree meets the standard usage }, and { contraindicated drug auditing items, whether all drug names and basic drugs of the drug person belong to contraindicated same drugs }; the drug-opening qualification auditing template comprises auditing items of drug-opening qualification and drug risk matching degree, and auditing rules are whether the drug-opening qualification is greater than or equal to the lowest drug-opening qualification allowed by the drug risk; the examination items and examination rules included in the diagnosis examination template are { medicine applicable disease examination items, whether the disease names and symptoms belong to medicine applicable diseases }, { adverse reaction examination items, whether the adverse reaction of the medicine can cause aggravation of basic diseases }.
203b, if the package prescription identification exists, obtaining a package auditing template of the current prescription to be checked, wherein the package auditing template comprises a package medicine set.
204b, extracting a to-be-checked medicine set of the current to-be-checked prescription, checking whether the to-be-checked medicine set is the same as the package medicine set, and if so, checking the current to-be-checked prescription by using the medicine checking template, the medication prescribing qualification checking template and the diagnosis checking template to obtain a template checking result.
Wherein, a doctor often selects a fixed medicine set (also a medicine set to be checked) to prescribe medicines to a patient, and in order to check whether the fixed medicine set (also the medicine set to be checked) selected by the doctor corresponds to a disease name and a certain symptom, a package checking template is configured, namely, the package checking template comprises a package medicine set corresponding to the certain disease name and a certain symptom, and the package medicine set is standard.
Specifically, the disease name and symptoms are extracted from the prescription to be audited currently, a set medicine set corresponding to the disease name and symptoms is found, the set medicine set comprises a standard medicine 1 and a standard medicine 2, the medicine name is extracted from the prescription to be audited currently and comprises a medicine name 1 and a medicine name 2, and whether the medicine name 1 and the medicine name 2 are the same as the standard medicine 1 and the standard medicine 2 is judged. If the current prescription to be checked is the same, checking the current prescription to be checked by using the medicine checking template, the prescribing qualification checking template and the diagnosis checking template in the step 204a of the embodiment to obtain a template checking result.
205. If the template auditing result is that the current prescription to be audited does not pass the template auditing, the current prescription to be audited and the non-passing template auditing item are sent to a manual auditing terminal, and the manual auditing result fed back by the manual auditing terminal is received.
206. If the manual checking result is that the current prescription to be checked does not pass the manual checking, the current prescription to be checked and the non-passing manual checking item are sent to a terminal of a medicine-providing person, an updated prescription to be checked fed back by the terminal of the medicine-providing person is received, and the updated prescription to be checked is checked by using the checking template, so that the checking result of the updated template is obtained.
Wherein, for embodiment steps 205 and 206, the relationship between the failed template audit item and the failed manual audit item is: if the manual audit is performed, all the non-passing template audit items are non-passing manual audit items, and if the non-passing template audit items are non-passing manual audit items, all the non-passing template audit items are non-passing manual audit items, and if the non-passing template audit items are not passing manual audit, all the non-passing template audit items are non-passing manual audit items.
Preferably, for the embodiment steps 205 and 206, if the result of the template audit is that the current prescription to be audited fails the template audit, the current prescription to be audited and the failed template audit item may be directly sent to the terminal of the drug issuer, the modification information of the failed template audit item fed back by the terminal of the drug issuer is received, then the audit template corresponding to the failed template audit item is obtained, the modification information is audited by using the audit template corresponding to the failed template audit item, and the result that the modification information passes the audit or fails the audit is obtained, if not, the current prescription to be audited, the failed template audit item and the modification information are generated to the manual audit terminal for audit.
Specifically stated, the above prescription auditing procedure first generates auditing templates including a package auditing template, a drug auditing template, a medication qualification auditing template, and a diagnostic auditing template, then saves the generated auditing templates to a Search analysis engine (e.g., an Elastic Search, ensuring high availability), and persists to a database (to prevent the auditing templates from being lost). When the method is specifically applied, firstly, a drug issuer generates a current prescription to be checked through a drug issuer terminal, and then judges whether the prescription has a package prescription mark or not, wherein the result comprises two results, namely the package prescription mark and the no package prescription mark:
1. for the package prescription mark, checking by using a package checking template, and if the package checking template passes, transmitting the current prescription to be checked to a medicine checking template, a medication prescribing qualification checking template and a diagnosis checking template to check, so as to obtain checking results of passing or failing the two templates; 12. if the package auditing template is not audited, the current prescription to be audited is not required to be sent to the medicine auditing template, the medication qualification auditing template and the diagnosis auditing template for auditing, and the non-passing template auditing result is directly obtained.
2. And for no package prescription mark, directly utilizing a medicine auditing template, a medicine prescribing qualification auditing template and a diagnosis auditing template to audit, and obtaining auditing results of passing or failing the two templates.
And if the template auditing result is not passed, the current prescription to be audited and the non-passing template auditing item are sent to the manual auditing terminal to obtain two manual auditing results which are passed or not passed, and if the template auditing result is not passed, the current prescription to be audited and the non-passing manual auditing item are sent to the issuer auditing terminal to be reissued, so that the updated prescription to be audited is obtained, and then the updated prescription to be audited is audited according to the same flow.
The prescription auditing method, device and equipment provided by the application can firstly acquire the current prescription to be audited; and further identifying whether the current prescription to be audited has a package prescription identification, if the current prescription to be audited does not have the package prescription identification, acquiring a medicine audit template, a prescribing qualification audit template and a diagnosis audit template, utilizing the medicine audit template, the prescribing qualification audit template and the diagnosis audit template to audit the current prescription to be audited to obtain a template audit result, if the current prescription to be audited has the package prescription identification, acquiring a package audit template of the current prescription to be audited, wherein the package audit template comprises a package medicine set, extracting whether the package medicine set of the current prescription to be audited is the same as the package medicine set, if the package medicine set is the same as the prescribing medicine set, utilizing the medicine audit template, the prescribing qualification audit template and the diagnosis audit template to obtain a template result, then, if the template result is the current prescription to be audited, transmitting the current prescription to a manual terminal and the manual terminal and not passing through the prescribing inspection terminal, and finally, receiving the manual feedback result to be updated by the manual terminal. According to the technical scheme, the current prescription to be audited is audited automatically according to the audit template which is constructed in advance, and the type of the current prescription to be audited (whether the prescription identification exists or not) is considered by the audit template, so that the efficiency of automatic audit is further improved, and the waiting time of a patient is reduced. On the basis of automatic auditing, manual auditing is used for prescriptions which do not pass, accuracy and safety are ensured, auditing time of auditing personnel is saved, and the problem of insufficient resources of the auditing personnel is relieved.
Further, as a specific implementation of the method shown in fig. 1 and fig. 2, an embodiment of the present application provides a prescription auditing apparatus, as shown in fig. 3, including: the first acquisition module 31, the second acquisition module 32 and the template auditing module 33;
a first obtaining module 31, configured to obtain a current prescription to be checked;
a second obtaining module 32, configured to obtain an audit template of the currently pending prescription, where the audit template is previously constructed based on audit items, audit rules, and specification data;
and the template auditing module 33 is used for auditing the currently-to-be-audited prescription by using the auditing template to obtain a template auditing result.
Accordingly, in order to obtain the review template of the current prescription to be reviewed, the second obtaining module 32 may specifically be configured to identify whether the current prescription to be reviewed has a package prescription identifier; if the package prescription mark is not provided, a medicine auditing template, a medication prescribing qualification auditing template and a diagnosis auditing template are obtained, wherein the auditing items included in the medicine auditing template are applicable crowd auditing items, usage quantity auditing items and tabu medicine auditing items, the auditing items included in the medication prescribing qualification auditing template are medication prescribing qualification and medicine risk matching degree auditing items, and the auditing items included in the diagnosis auditing template are medicine applicable disease auditing items and basic disease aggravating auditing items caused by medicine adverse reactions.
Accordingly, in order to review the current prescription to be reviewed using the review template, the template review module 33 is specifically configured to review the current prescription to be reviewed using the drug review template, the prescribing qualification review template, and the diagnostic review template.
Correspondingly, in order to obtain the review template of the prescription to be reviewed currently, the second obtaining module 32 may be specifically further configured to obtain a package review template of the prescription to be reviewed currently if the package prescription identifier is provided, where the package review template includes a package drug set.
Accordingly, in order to audit the currently-to-be-audited prescription using the audit template, the template audit module 33 may be specifically configured to extract a to-be-audited drug set of the currently-to-be-audited prescription; checking whether the drug set to be checked is the same as the package drug set; and if the current prescription to be audited is the same, utilizing the medicine audit template, the medication prescribing qualification audit template and the diagnosis audit template to audit the current prescription to be audited.
In a specific application scenario, as shown in fig. 4, a prescription auditing apparatus further includes: the manual review module 34 is specifically configured to send the current prescription to be reviewed and the non-passing template review item to a manual review terminal if the template review result indicates that the current prescription to be reviewed does not pass the template review; and receiving a manual auditing result fed back by the manual auditing terminal.
Accordingly, as shown in fig. 4, a prescription auditing apparatus further includes: the updating module 35 is specifically configured to send the current prescription to be checked and the non-passing manual checking item to a terminal of a drug issuer if the manual checking result indicates that the current prescription to be checked does not pass the manual checking; receiving an updated prescription to be checked fed back by the terminal of the prescriber; and auditing the updated prescription to be audited by utilizing the auditing template to obtain an auditing result of the updated template.
In a specific application scenario, as shown in fig. 4, a prescription auditing apparatus further includes: the generating module 36 is specifically configured to receive a configuration of the audit item and the corresponding audit rule; extracting specification data corresponding to each drug and each type of auditing item from a drug information base; and generating the auditing template according to each type of auditing item, the corresponding auditing rule and the specification data.
In a specific application scenario, as shown in fig. 4, a prescription auditing apparatus further includes: the configuration module 37 is specifically configured to configure a prescription template, where the prescription template includes: the system comprises a prescriber qualification field, a prescriber field, a diagnosis field, a medication field and a package prescription mark, wherein the prescriber field comprises a prescriber group field, a prescriber basic disease field and a prescriber basic medication field, the diagnosis field comprises a disease name field, a symptom field and a disease degree field, and the medication field comprises a medicine name field, a medicine usage amount field and a medicine risk field; and responding to the acquisition request and the information filling request of the prescription template to obtain the currently pending prescription.
It should be noted that, other corresponding descriptions of each functional unit related to the prescription auditing apparatus provided in this embodiment may refer to corresponding descriptions of fig. 1 to 2, and are not described herein again.
Based on the above method shown in fig. 1 to 2, correspondingly, the present embodiment further provides a storage medium, which may be specifically volatile or nonvolatile, and has a computer program stored thereon, where the program is executed by a processor to implement the above method for checking prescriptions shown in fig. 1 to 2.
Based on such understanding, the technical solution of the present application may be embodied in the form of a software product, which may be stored in a storage medium (may be a CD-ROM, a U-disk, a mobile hard disk, etc.), and includes several instructions for causing a computer device (may be a personal computer, a server, or a network device, etc.) to execute the method of each implementation scenario of the present application.
Based on the method shown in fig. 1 to 2 and the virtual device embodiments shown in fig. 3 and 4, in order to achieve the above object, the present embodiment further provides a computer device, where the computer device includes a storage medium and a processor; a storage medium storing a computer program; a processor for executing a computer program to implement the prescription auditing method described above and shown in fig. 1-2.
Optionally, the computer device may also include a user interface, a network interface, a camera, radio Frequency (RF) circuitry, sensors, audio circuitry, WI-FI modules, and the like. The user interface may include a Display screen (Display), an input unit such as a Keyboard (Keyboard), etc., and the optional user interface may also include a USB interface, a card reader interface, etc. The network interface may optionally include a standard wired interface, a wireless interface (e.g., WI-FI interface), etc.
It will be appreciated by those skilled in the art that the architecture of a computer device provided in this embodiment is not limited to this physical device, but may include more or fewer components, or may be combined with certain components, or may be arranged in a different arrangement of components.
The storage medium may also include an operating system, a network communication module. An operating system is a program that manages the computer device hardware and software resources described above, supporting the execution of information handling programs and other software and/or programs. The network communication module is used for communication among components in the actual storage medium and communication with other hardware and software in the information processing entity device.
From the above description of the embodiments, it will be apparent to those skilled in the art that the present application may be implemented by means of software plus necessary general hardware platforms, or may be implemented by hardware.
The prescription auditing method, device and equipment provided by the application can firstly acquire the current prescription to be audited; further acquiring an auditing template of the current prescription to be audited, wherein the auditing template is constructed in advance based on auditing items, auditing rules and specification data; finally, the current prescription to be checked is checked by using the checking template, and a template checking result is obtained. According to the technical scheme, the current prescription to be checked is automatically checked according to the pre-constructed checking template, manual checking is not needed, checking efficiency is high, accuracy is high, and cost is low.
Those skilled in the art will appreciate that the drawing is merely a schematic illustration of a preferred implementation scenario and that the modules or flows in the drawing are not necessarily required to practice the application. Those skilled in the art will appreciate that modules in an apparatus in an implementation scenario may be distributed in an apparatus in an implementation scenario according to an implementation scenario description, or that corresponding changes may be located in one or more apparatuses different from the implementation scenario. The modules of the implementation scenario may be combined into one module, or may be further split into a plurality of sub-modules.
The above-mentioned inventive sequence numbers are merely for description and do not represent advantages or disadvantages of the implementation scenario. The foregoing disclosure is merely illustrative of some embodiments of the application, and the application is not limited thereto, as modifications may be made by those skilled in the art without departing from the scope of the application.
Claims (10)
1. A method of prescription auditing, the method comprising:
acquiring a current prescription to be checked;
obtaining an auditing template of the current prescription to be audited, wherein the auditing template is constructed in advance based on auditing items, auditing rules and specification data;
and utilizing the auditing template to audit the current prescription to be audited to obtain a template auditing result.
2. The method of claim 1, wherein the obtaining an audit template for the current prescription to be audited comprises:
identifying whether the current prescription to be checked has a package prescription identification;
if the package prescription mark is not provided, a medicine auditing template, a medication prescribing qualification auditing template and a diagnosis auditing template are obtained, wherein the auditing items included in the medicine auditing template are applicable crowd auditing items, usage quantity auditing items and tabu medicine auditing items, the auditing items included in the medication prescribing qualification auditing template are medication prescribing qualification and medicine risk matching degree auditing items, and the auditing items included in the diagnosis auditing template are medicine applicable disease auditing items and basic disease aggravating auditing items caused by medicine adverse reactions;
the method for auditing the currently-to-be-audited prescription by utilizing the auditing template comprises the following steps:
and checking the current prescription to be checked by using the medicine checking template, the medication prescribing qualification checking template and the diagnosis checking template.
3. The method according to claim 2, characterized in that the method further comprises:
if the package prescription identification exists, obtaining a package auditing template of the current prescription to be audited, wherein the package auditing template comprises a package medicine set;
the method for auditing the currently-to-be-audited prescription by utilizing the auditing template comprises the following steps:
extracting a to-be-checked medicine set of the current to-be-checked prescription;
checking whether the drug set to be checked is the same as the package drug set;
and if the current prescription to be audited is the same, utilizing the medicine audit template, the medication prescribing qualification audit template and the diagnosis audit template to audit the current prescription to be audited.
4. A method according to any one of claims 1-3, further comprising:
if the template auditing result is that the current prescription to be audited fails the template auditing, the current prescription to be audited and the non-template auditing item are sent to a manual auditing terminal;
and receiving a manual auditing result fed back by the manual auditing terminal.
5. The method according to claim 4, further comprising:
if the manual auditing result is that the current prescription to be audited does not pass the manual auditing, the current prescription to be audited and the non-passing manual auditing item are sent to a terminal of a drug issuer;
receiving an updated prescription to be checked fed back by the terminal of the prescriber;
and auditing the updated prescription to be audited by utilizing the auditing template to obtain an auditing result of the updated template.
6. The method of claim 1, further comprising, prior to said obtaining an audit template for said currently pending prescription:
receiving configuration of auditing items and corresponding auditing rules;
extracting specification data corresponding to each drug and each type of auditing item from a drug information base;
and generating the auditing template according to each type of auditing item, the corresponding auditing rule and the specification data.
7. The method of claim 1, further comprising, prior to said obtaining the currently pending prescription:
configuring a prescription template, wherein the prescription template comprises: the system comprises a prescriber qualification field, a prescriber field, a diagnosis field, a medication field and a package prescription mark, wherein the prescriber field comprises a prescriber group field, a prescriber basic disease field and a prescriber basic medication field, the diagnosis field comprises a disease name field, a symptom field and a disease degree field, and the medication field comprises a medicine name field, a medicine usage amount field and a medicine risk field;
and responding to the acquisition request and the information filling request of the prescription template to obtain the currently pending prescription.
8. A prescription auditing apparatus, the apparatus comprising:
the first acquisition module is used for acquiring a current prescription to be checked;
the second acquisition module is used for acquiring an audit template of the current prescription to be audited, wherein the audit template is constructed in advance based on audit items, audit rules and specification data;
and the template auditing module is used for auditing the current prescription to be audited by utilizing the auditing template to obtain a template auditing result.
9. A storage medium having stored thereon a computer program, which when executed by a processor implements the prescription auditing method of any of claims 1 to 7.
10. A computer device comprising a storage medium, a processor and a computer program stored on the storage medium and executable on the processor, characterized in that the processor implements the prescription auditing method of any of claims 1 to 7 when the computer program is executed by the processor.
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| CN202311205276.9A CN117238435A (en) | 2023-09-18 | 2023-09-18 | Prescription auditing method, device and equipment |
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| CN202311205276.9A CN117238435A (en) | 2023-09-18 | 2023-09-18 | Prescription auditing method, device and equipment |
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