CN112116239A - Method for realizing medicine standardization - Google Patents
Method for realizing medicine standardization Download PDFInfo
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- CN112116239A CN112116239A CN202010973979.6A CN202010973979A CN112116239A CN 112116239 A CN112116239 A CN 112116239A CN 202010973979 A CN202010973979 A CN 202010973979A CN 112116239 A CN112116239 A CN 112116239A
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- 239000003814 drug Substances 0.000 title claims abstract description 122
- 238000000034 method Methods 0.000 title claims abstract description 34
- 229940079593 drug Drugs 0.000 claims abstract description 49
- 230000008569 process Effects 0.000 claims description 12
- 238000004883 computer application Methods 0.000 abstract description 2
- 239000002552 dosage form Substances 0.000 description 4
- 238000012423 maintenance Methods 0.000 description 4
- 238000006243 chemical reaction Methods 0.000 description 2
- 238000010586 diagram Methods 0.000 description 2
- 238000005429 filling process Methods 0.000 description 2
- 238000004806 packaging method and process Methods 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 238000013459 approach Methods 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 238000007689 inspection Methods 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 230000007246 mechanism Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000012544 monitoring process Methods 0.000 description 1
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- G—PHYSICS
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- G06Q—INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR ADMINISTRATIVE, COMMERCIAL, FINANCIAL, MANAGERIAL OR SUPERVISORY PURPOSES; SYSTEMS OR METHODS SPECIALLY ADAPTED FOR ADMINISTRATIVE, COMMERCIAL, FINANCIAL, MANAGERIAL OR SUPERVISORY PURPOSES, NOT OTHERWISE PROVIDED FOR
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- G06F16/953—Querying, e.g. by the use of web search engines
- G06F16/9535—Search customisation based on user profiles and personalisation
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- G—PHYSICS
- G06—COMPUTING; CALCULATING OR COUNTING
- G06Q—INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR ADMINISTRATIVE, COMMERCIAL, FINANCIAL, MANAGERIAL OR SUPERVISORY PURPOSES; SYSTEMS OR METHODS SPECIALLY ADAPTED FOR ADMINISTRATIVE, COMMERCIAL, FINANCIAL, MANAGERIAL OR SUPERVISORY PURPOSES, NOT OTHERWISE PROVIDED FOR
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Abstract
The invention provides a method for realizing drug standardization, belonging to the technical field of computer application, and the method comprises two parts: 1) medicine filling and 2) medicine adding. If standard data are obtained according to condition recommendation, selecting specific standard data and filling the basic medicine data content; and if the standard data is not acquired or the standard data information is incorrect and incomplete, manually filling the data content of the basic medicine. Meanwhile, intelligent combined filling is carried out aiming at specific data content. And for the medicines with the missing basic medicine data, adding the medicines according to standard data, or adding the medicines according to the combination of multi-source data and the basic medicine data.
Description
Technical Field
The invention relates to a computer application technology, in particular to a method for realizing drug standardization.
Background
The drug standard refers to the pharmacopoeia of the people's republic of China, drug registration standards and other drug standards issued by the State food and drug administration (abbreviated as food and drug administration), and the content of the drug standard includes technical requirements such as quality indexes, inspection methods and production processes.
At present, the national drug standard management has no formation system, and mostly refers to the drug standard only, so that the responsibility subject of the drug standard is not clear; each link of the drug standard and the drug monitoring chain is broken; the guarantee mechanism of the drug standard is lacking; measures for promoting the standard development of the medicine are not matched; loss of historical data, and the like.
The existing basic drug data can not meet the requirements of drug data treatment process, and the main problems include incomplete basic drug data content, missing historical basic drug data and the like, so that the basic drug data needs to be standardized. And the manual coring and checking of standard medicine data and the filling of historical missing data are tedious, time-consuming, easy-to-miss and challenging works.
Disclosure of Invention
In order to solve the technical problems, the invention provides a method for realizing drug standardization, and aims to help people to quickly and manually perfect standardized drug information, quickly and effectively increase historical missing data, save manpower and improve standardization efficiency.
The technical scheme of the invention is as follows:
a method for achieving drug standardization, comprising two parts: 1) drug filling and 2) drug addition
1) Filling the medicine:
1.1) selecting a basic medicine to obtain a retrieval condition;
1.2) searching standard medicines, and filling if the standard medicines are searched;
1.3) selecting data to fill up; then standard medicines are filled;
1.4) storing;
1.5) finishing;
in the step 1.2), if the retrieval is not achieved, determining whether the retrieval is the final retrieval condition, otherwise, re-obtaining the retrieval condition; if yes, then padding is selected and step 1.4) is filled in manually.
And if the final search condition is not selected to fill up, the method is finished directly.
In step 1.2), if the search result shows that the padding is not carried out, the process is directly finished.
In step 1.3), if data padding is not selected, manual padding is performed, and then step 1.4) is performed.
2) Newly adding medicines:
2.1) selecting the basic drug based on the filling data of the basic drug
If the data is not filled by the basic medicines, searching the standard medicines, returning to the step 2.5 after selecting the standard medicines, and if not, directly ending the process.
2.2) obtaining a retrieval condition and retrieving a standard medicine;
2.3) if the standard medicine is searched, selecting a new data to select the standard medicine; directly ending without selection;
if not, determining whether the condition is the final retrieval condition, and if not, returning to the step 2.2); if yes, whether the new addition is selected or not is determined. If new addition is not selected, the process is directly finished, if new addition is selected, basic medicine data is modified manually, and then the process goes to step 2.4).
If the data retrieved but not selected for adding is new, the basic drug data is modified manually, and then the step 2.4) is returned.
2.4) filling up basic medicine information;
2.5) newly adding;
2.6) end.
In the step 2.3), the step of the method,
the invention has the advantages that
1. The invention has complete recommendation rules of standard medicine data, supports various recommendation combinations, reduces the recommendation of invalid data, reduces the invalid retrieval of recommended data, and plays the roles of liberating manpower and improving the standardization accuracy.
2. The invention supports standard data to fill up basic medicine data, and greatly improves the convenience and effectiveness of standardization.
3. The invention supports the standard data to newly add basic medicine data, avoids the omission of historical medicine information and ensures the maintenance efficiency.
4. The invention supports manual filling of basic medicine data and ensures the complete maintainability of the data.
5. The invention supports the manual addition of basic drug data, avoids the condition that the missing historical drug information cannot be maintained, and ensures the integrity of data maintenance.
6. The invention provides an intelligent combined specification, and maintains the normative and consistency of the data specification of the basic medicine.
Drawings
FIG. 1 is a schematic diagram of a drug filling process;
FIG. 2 is a schematic diagram of a drug addition process;
FIG. 3 is a drug maintenance method overview of the present invention.
Detailed Description
In order to make the objects, technical solutions and advantages of the embodiments of the present invention clearer and more complete, the technical solutions in the embodiments of the present invention will be described below with reference to the drawings in the embodiments of the present invention, and it is obvious that the described embodiments are some, but not all, embodiments of the present invention, and based on the embodiments of the present invention, all other embodiments obtained by a person of ordinary skill in the art without creative efforts belong to the scope of the present invention.
The method recommends standard medicine information according to the basic medicine data information and condition levels, and performs standard maintenance on the basic medicine data in a mode of combining standard data perfection, intelligent combination and manual filling. If standard data are obtained according to condition recommendation, selecting specific standard data and filling the basic medicine data content; and if the standard data is not acquired or the standard data information is incorrect and incomplete, manually filling the data content of the basic medicine. Meanwhile, intelligent combined filling is carried out aiming at specific data content. For the medicine with missing basic medicine data, the function flow mainly related by the invention is newly added according to standard data and comprises two parts: drug filling and drug adding.
The main problems of the current basic medicine data are inaccuracy, imperfection and historical data missing, so the inaccuracy and imperfection data need to be filled, and the missing historical data needs to be increased.
1. Drug filling process description (as shown in figure 1).
The drug filling takes basic drugs as a reference, standard data are obtained through data recommendation based on basic drug data, and multiple approaches are selected for filling.
A. Semi-automatic filling: after standard data are obtained through data recommendation based on basic medicine data, correct and complete standard data are selected to automatically fill information, and if dosage forms, concentrations, contents, content units, capacity units, conversion coefficients, preparation units and packaging units exist in the filling information, the combined medicine specification operation is performed according to the rules of intelligent combined specifications.
B. Manual filling: after standard data are obtained through data recommendation based on basic medicine data, the basic medicine data are directly filled, further filling is performed after semi-automatic filling, and in the process, the basis for manual filling comes from other data such as food and drug administration. And if the filling information comprises dosage form, concentration, content unit, capacity unit, conversion coefficient, preparation unit and packaging unit, combining the pharmaceutical specifications according to the rule of the intelligent combined specification.
2. The drug addition process is illustrated (as shown in fig. 2).
The drug filling takes standard data as a reference, and a plurality of ways are selected for newly adding.
A. Newly adding a foundation: and selecting more than or equal to one piece of standard data in the standard data list to newly add the basic medicine. When the new medicine is added, the medicine is uniquely identified according to the name, the common name, the trade name, the manufacturer, the dosage form, the concentration, the content unit, the capacity unit and other contents of the medicine, and if basic medicines with the same information exist, the new medicine is not added.
B. Newly adding in combination: the newly-added combination is to combine basic medicine data and standard data, firstly determine the basic medicine, and obtain the standard data through data recommendation based on the basic medicine data. And then, selecting more than or equal to one piece of standard data to be newly added in batch, filling the missing fields with the content of the basic medicine data based on the standard data, and combining the medicine specifications according to the rule of the intelligent combination specification. When the new medicine is added, the medicine is uniquely identified according to the name, the common name, the trade name, the manufacturer, the dosage form, the concentration, the content unit, the capacity unit and the like of the medicine, and if the medicine exists, the new medicine is not added.
The above description is only a preferred embodiment of the present invention, and is only used to illustrate the technical solutions of the present invention, and not to limit the protection scope of the present invention. Any modification, equivalent replacement, or improvement made within the spirit and principle of the present invention shall fall within the protection scope of the present invention.
Claims (9)
1. A method for realizing drug standardization is characterized in that,
the device comprises two parts: 1) drug filling and 2) drug addition
1) The filling steps of the medicine are as follows:
1.1) selecting a basic medicine to obtain a retrieval condition;
1.2) searching standard medicines, and filling if the standard medicines are searched;
1.3) selecting data to fill up; then standard medicines are filled;
1.4) storing;
1.5) finishing;
2) the new medicine adding steps are as follows:
2.1) selecting a basic medicine according to the basic medicine filling data;
2.2) obtaining a retrieval condition and retrieving a standard medicine;
2.3) if the standard medicine is searched, selecting a new data to select the standard medicine; directly ending without selection;
2.4) filling up basic medicine information;
2.5) newly adding;
2.6) end.
2. The method of claim 1,
in the step 1.2), if the retrieval is not achieved, determining whether the retrieval is the final retrieval condition, otherwise, re-obtaining the retrieval condition; if yes, padding is selected and a jump to step 1.4) is made by manual padding.
3. The method of claim 2,
and if the final search condition is not selected to fill up, the method is finished directly.
4. The method of claim 1,
in step 1.2), if the search result shows that the padding is not carried out, the process is directly finished.
5. The method of claim 1,
in step 1.3), if data padding is not selected, manual padding is performed, and then step 1.4) is performed.
6. The method of claim 1,
in step 2.1), if the data is not filled up by the basic medicine, the standard medicine is searched, the step 2.5 is returned after the standard medicine is selected), and if the data is not selected, the process is directly finished.
7. The method of claim 1,
in the step 2.3), if the retrieval is not available, determining whether the retrieval is the final retrieval condition, otherwise, returning to the step 2.2); if yes, it is determined whether a new addition is selected.
8. The method of claim 7,
if new addition is not selected, the process is directly finished, if new addition is selected, basic medicine data is modified manually, and then the process goes to step 2.4).
9. The method of claim 7,
in step 2.3), if the data is retrieved but not selected to be newly added, the basic medicine data is modified manually, and then the step 2.4) is returned.
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| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN202010973979.6A CN112116239A (en) | 2020-09-16 | 2020-09-16 | Method for realizing medicine standardization |
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| Application Number | Priority Date | Filing Date | Title |
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| CN202010973979.6A CN112116239A (en) | 2020-09-16 | 2020-09-16 | Method for realizing medicine standardization |
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Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN103455608A (en) * | 2013-09-05 | 2013-12-18 | 广东医药价格协会 | Management and inquiry system based on medicine coding |
| CN107784058A (en) * | 2017-04-11 | 2018-03-09 | 平安医疗健康管理股份有限公司 | Drug data processing method and processing device |
| CN107818124A (en) * | 2017-03-03 | 2018-03-20 | 平安医疗健康管理股份有限公司 | Data matching method and device |
| CN111125076A (en) * | 2019-12-17 | 2020-05-08 | 武汉海云健康科技股份有限公司 | Big data based medicine universal name cleaning method and system, server and medium |
| CN111180087A (en) * | 2020-01-02 | 2020-05-19 | 中国中医科学院中医药信息研究所 | Marketing medicine information standardization method, equipment, server and storage medium |
-
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- 2020-09-16 CN CN202010973979.6A patent/CN112116239A/en active Pending
Patent Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN103455608A (en) * | 2013-09-05 | 2013-12-18 | 广东医药价格协会 | Management and inquiry system based on medicine coding |
| CN107818124A (en) * | 2017-03-03 | 2018-03-20 | 平安医疗健康管理股份有限公司 | Data matching method and device |
| CN107784058A (en) * | 2017-04-11 | 2018-03-09 | 平安医疗健康管理股份有限公司 | Drug data processing method and processing device |
| CN111125076A (en) * | 2019-12-17 | 2020-05-08 | 武汉海云健康科技股份有限公司 | Big data based medicine universal name cleaning method and system, server and medium |
| CN111180087A (en) * | 2020-01-02 | 2020-05-19 | 中国中医科学院中医药信息研究所 | Marketing medicine information standardization method, equipment, server and storage medium |
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Application publication date: 20201222 |