CN107784610A - Basic drug information proofreading method and device - Google Patents
Basic drug information proofreading method and device Download PDFInfo
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Abstract
The present invention relates to a kind of Basic drug information proofreading method and device.Basic drug information proofreading method, which specifically includes, obtains latest edition medicine information data, the medicine information for carrying out data check and correction is needed to record in identification latest edition medicine information data, identify this bit code information in medicine information record, judge whether medicine information record meets automatic Proofreading condition according to this bit code information, when medicine information record meets automatic Proofreading condition, specification data and formulation data are extracted from medicine this bit code memo field in medicine information record according to default extracting rule, specs field and formulation field in being recorded according to specification data and formulation data to medicine information are proofreaded and generate collation, operation corresponding with collation is carried out to medicine information record.The above method and device are capable of the operating efficiency of the check and correction process of Basic drug information.
Description
Technical field
The present invention relates to field of computer technology, more particularly to a kind of Basic drug information proofreading method and device.
Background technology
The foundation in medicine information storehouse is easy to medical and health personel to inquire about, compared and analyze the essential information of medicine,
Data basis is provided for clinical rational drug use.
Medicine information storehouse needs periodically to be updated drug data, and medicine occurs during medicine information updates
Essential information lose, missing or the situation for mistake occur, the drug data for causing medicine information storehouse to be included is imperfect.Typically
, be all that Basic drug information is proofreaded one by one by the method for hand inspection, find essential information occur mistake or not
Complete drug data, still, the method manually proofreaded need to expend substantial amounts of manpower and time, and efficiency is very low.
The content of the invention
Based on this, it is necessary to for above-mentioned Basic drug information check and correction process efficiency it is low the problem of, there is provided a kind of medicine
Essential information proofreading method and device.
A kind of Basic drug information proofreading method, the described method comprises the following steps：
Obtain latest edition medicine information data；
Identify the medicine information record for needing to carry out data check and correction in the latest edition medicine information data；
This bit code information in the medicine information record is identified, the medicine information is judged according to described bit code information
Whether record meets automatic Proofreading condition；
When medicine information record meets the automatic Proofreading condition, believed according to default extracting rule from the medicine
Specification data and formulation data are extracted in medicine this bit code memo field in breath record；
Specs field and formulation word in being recorded according to the specification data and the formulation data to the medicine information
Duan Jinhang is proofreaded and is generated collation, and operation corresponding with the collation is carried out to medicine information record.
In one of the embodiments, this bit code information in the identification medicine information record, according to described
Bit code information judges that the step of whether the medicine information record meets automatic Proofreading condition includes：
Identify this bit code and medicine this bit code memo field that medicine one's own department or unit code field includes in the medicine information record
In this bit code remarks unit；
Format check is carried out to described bit code and described bit code remarks unit；
When the form of described bit code and the form of described bit code remarks unit meet preset format, described in judgement
Whether the quantity of this bit code and the quantity of described bit code remarks unit are equal and be all higher than 1；If so, the medicine information record
Meet automatic Proofreading condition.
In one of the embodiments, the basis presets extracting rule from medicine one's own department or unit in medicine information record
The step of extracting specification data and formulation data in code memo field includes：
Medicine this bit code memo field is split as multiple bit code remarks units；
Extract the remarks data in described bit code remarks unit；
Identify the extraction identifier in the remarks data；
The remarks data are split according to the extraction identifier；
Judge the data type of the remarks data after splitting；
Default extracting rule corresponding with the extraction identifier is obtained, according to the default extracting rule and the data
Type extracts the specification data and the formulation data from described bit code remarks unit.
In one of the embodiments, methods described also includes：
When in the remarks data without extraction identifier, judge whether include specification character in the remarks data,
When including specification character in the remarks data, the remarks data are extracted as specification data；When in the remarks data
During not comprising specification character, the remarks data are extracted as formulation data；
The step of data type of the remarks data after the judgement fractionation, includes：
Judge whether include specification character in the remarks data after splitting；
When including the specification character in the remarks data after fractionation, the data of the remarks data after fractionation
Type is specification；When not including the specification character in the remarks data after fractionation, the remarks data after fractionation
Data type be formulation.
In one of the embodiments, it is described that the medicine information is remembered according to the specification data and the formulation data
Specs field and formulation field in record are proofreaded and generate collation, and medicine information record is carried out and the school
To including corresponding to result the step of operation：
The specification data and the specs field are subjected to consistency desired result and obtain specification check results；
The formulation data and the formulation field are subjected to consistency desired result and obtain formulation check results；
Specification problem mark is carried out for abnormal medicine information record to the specification check results, the formulation is verified
As a result formulation problem mark is carried out for abnormal medicine information record；
The medicine information for being labeled with specification problem and/or formulation problem record is sent to auditor.
In one of the embodiments, it is described to obtain the specification data and specs field progress consistency desired result
The step of specification check results, includes：
The specs field is split as specification unit, judging the quantity of the quantity and the specification data of specification unit is
It is no equal；
If unequal, specification exception check results are generated；If equal, the specification data and the specification unit are carried out
Match one by one, when in the absence of the specification unit to match with the specification data, generate specification exception check results；
It is described that the formulation data and formulation field progress consistency desired result are obtained into the rapid bag of formulation check results
Include：
The formulation field is split as dosage form units, judging the quantity of the quantity and the formulation data of dosage form units is
It is no equal；
If unequal, formulation exception check results are generated；It is crucial from the formulation extracting data formulation respectively if equal
Word, the formulation keyword is matched one by one with the dosage form units, matched when in the absence of with the formulation keyword
Dosage form units when, generate formulation exception check results.
A kind of Basic drug information verifying unit, described device include：
Data acquisition module, for obtaining latest edition medicine information data；
Identification module, for identifying the medicine information for needing to carry out data check and correction in the latest edition medicine information data
Record；
Automatic Proofreading judge module, for identifying this bit code information in the medicine information record, according to described one's own department or unit
Code information judges whether the medicine information record meets automatic Proofreading condition；
Extraction module, extracting rule is preset from medicine this bit code memo field in medicine information record for basis
Middle extraction specification data and formulation data；
Checking module, for the specification in being recorded according to the specification data and the formulation data to the medicine information
Field and formulation field are proofreaded and generate collation, medicine information record are carried out corresponding with the collation
Operation.
In one of the embodiments, the automatic Proofreading judge module includes：
Unit identification module, for identifying medicine one's own department or unit code field includes in medicine information record this bit code and medicine
This bit code remarks unit in product this bit code memo field；
Format check module, for carrying out format check to described bit code and described bit code remarks unit；
Quantity correction verification module, for when the form of described bit code and the form of described bit code remarks unit meet it is pre-
If during form, judge described bit code quantity and described bit code remarks unit quantity it is whether equal and be all higher than 1；If
It is that the medicine information record satisfaction automatically extracts condition.
In one of the embodiments, the extraction module includes：
Unit splits module, for medicine this bit code memo field to be split as into multiple bit code remarks units；
Remarks extraction module, for extracting the remarks data in described bit code remarks unit；
Identifier identification module, for identifying the extraction identifier in the remarks data；
Data split module, for being split according to the extraction identifier to the remarks data；
Type judging module, for judging the data type of the remarks data after splitting；
Data extraction module, for obtaining default extracting rule corresponding with the extraction identifier, according to described default
Extracting rule and the data type extract the specification data and the formulation data from described bit code remarks unit.
In one of the embodiments, the checking module includes：
Specification correction verification module, specification school is obtained for the specification data and the specs field to be carried out into consistency desired result
Test result；
Formulation correction verification module, formulation school is obtained for the formulation data and the formulation field to be carried out into consistency desired result
Test result；
Problem labeling module, for carrying out specification problem mark to the specification check results for abnormal medicine information record
Note, formulation problem mark is carried out for abnormal medicine information record to the formulation check results；
Sending module, it is careful for the medicine information record for being labeled with specification problem and/or formulation problem to be sent to
Core personnel.
Above-mentioned Basic drug information proofreading method and device, recorded by the medicine information for judging to need to carry out data check and correction
Whether automatic Proofreading condition is met, and this bit code of medicine memo field in being recorded to qualified medicine information carries according to default
Automatically extracting for regular progress specification data and formulation data is taken, and according to the data after extraction to the rule in medicine information record
Lattice field and formulation field are proofreaded, and are automatically generated collation and are carried out respective handling to drug data, so as to realize medicine
The automatic business processing of product Information Proofreading process, saves manpower and proof time, effectively increases correction efficiency.
Brief description of the drawings
Fig. 1 is the flow chart of Basic drug information proofreading method in one embodiment；
Fig. 2 is the internal structure schematic diagram for being used to perform the terminal of Basic drug information proofreading method in one embodiment；
Fig. 3 is the structural representation of Basic drug information verifying unit in one embodiment；
Fig. 4 is the structural representation of automatic Proofreading judge module in one embodiment；
Fig. 5 is the structural representation of extraction module in one embodiment；
Fig. 6 is the structural representation of checking module in one embodiment.
Embodiment
In order to make the purpose , technical scheme and advantage of the present invention be clearer, it is right below in conjunction with drawings and Examples
The present invention is further elaborated.It should be appreciated that specific embodiment described herein is only to explain the present invention, not
For limiting the present invention.
In one embodiment, as shown in Figure 1, there is provided a kind of Basic drug information proofreading method, this method can be applied
In terminal or server, in this way applied to being illustrated exemplified by terminal, the described method comprises the following steps：
Step 110, latest edition medicine information data are obtained.
Terminal downloads newest medicine information data with to the medicine stored in terminal from authoritative medicine information issuing web site
Product information data is updated.The medicine information data for retaining original version in terminal simultaneously are easy to user to consult contrast.Enter one
Step, after terminal downloads newest medicine information data, latest data version number is automatically generated, when user inputs latest data
Latest edition medicine information data can be checked during version number.In one embodiment, the medicine information data of each version can
To be stored in the medicine information database of terminal.
Medicine information issuing web site is generally the medical WEB of authority, for example, state food pharmaceuticals administration general bureau net
Stand, Bureau of Drugs Supervision periodically can be updated to the medicine information of issue.Further, whether terminal meeting periodic detection Bureau of Drugs Supervision website
Medicine information is updated, when having detected renewal, terminal downloads the medicine information data of renewal automatically.
Recorded in medicine information data comprising a plurality of medicine information, each medicine information record corresponds to a kind of medicine.
It is basic comprising nomenclature of drug, medicine this bit code, this bit code of medicine remarks, formulation, specification, manufacturer etc. in medicine information record
Medicine information.
In one embodiment, terminal is standardized after obtaining medicine information data to medicine information data.Tool
Body, go out field name from medicine information extracting data, extracted in being recorded from each medicine information corresponding with field name
Content as field, generate the medicine information record of reference format so that the data format of every kind of medicine is unified, every record
Field corresponded with field name, be easy to checking and searching for drug data.
Step 120, the medicine information record for needing to carry out data check and correction in latest edition medicine information data is identified.
Every kind of medicine of Bureau of Drugs Supervision's approval all has unique authentication code, but the medicine of same authentication code may
With multiple this bit code of medicine, because different packagings may be used during marketing drugs, the specification of Different Package medicine,
Formulation is different, and each specification, the medicine of dosage form combination correspond to medicine this bit code.This bit code of medicine is by digital group
Into, but from medicine, this bit code can not understand the specification of corresponding medicine, dose-form information, and this bit code of medicine remarks are to corresponding medicine
The specification of the medicine of this bit code, dose-form information carry out remarks, and specification, the agent of medicine can be intuitively understood from this bit code of medicine remarks
Type information.
The medicine information of Bureau of Drugs Supervision's issue is up to more than 170,000, and specification, the agent of medicine occur during renewal
Type information is lost or incomplete situation, causes the medicine information data of terminal downloads that specification, dose-form information mistake also occurs
Or situation about losing.When the medicine of same authentication code medicine this bit code, this bit code of medicine remarks, specification and formulation data occur
Illustrate that the specification of medicine, type of dosage form have been likely occurred change during change, therefore, it is necessary to being likely to occur above-mentioned data variation
Medicine in specification, formulation checked.The medicine information data of original version have been subjected to verification of data, and therefore, terminal is only
Need to be to newly increasing medicine (i.e. newly-increased authentication code medicine) relative to original edition data in latest edition medicine information data
Medicine information records and authentication code is identical and it is any in medicine this bit code, this bit code of medicine remarks, specification and dose-form information
One medicine information record to change is checked.
Specifically, identification is as follows the step of needing to carry out the medicine information record of data check and correction, terminal obtains user's input
Versions of data number after, obtain original version medicine information number corresponding with versions of data number for storing in medicine information database
According to.Terminal first determines whether this bit code of medicine one's own department or unit code field of medicine information record and medicine in latest edition medicine information data
Whether memo field is empty, if being then empty medicine by either field in medicine one's own department or unit code field and medicine this bit code memo field
Product information record is transferred to artificial check and correction set.Medicine one's own department or unit code field and this bit code of medicine memo field are not empty medicine by terminal
Product information record finds out authentication code to increase newly compared with the medicine information record of original version medicine information data
Medicine information records, and identifies identical with original version authentication code field in redaction but medicine one's own department or unit code field, medicine
The medicine information record that either field changes in four this bit code memo field, specs field and formulation field fields.Eventually
The authentication code identified is held to be recorded as needing to carry out with the medicine information that field changes for newly-increased medicine information record
The medicine information record of data check and correction.
Step 130, this bit code information in medicine information record is identified, judges that medicine information records according to this bit code information
Whether automatic Proofreading condition is met.
Automatic Proofreading refers to medicine one's own department or unit code field in medicine information record and this bit code of medicine memo field meet it is pre-
If condition to the specification in record, formulation field so as to being proofreaded automatically by this bit code of medicine memo field.One's own department or unit
Code information includes this bit code of medicine information and medicine this bit code remark information, quantity and the specification, the quantity phase of formulation of this bit code
It is corresponding, specification, the specifying information of formulation are included in this bit code remarks.
The step of whether the medicine information record that terminal judges to need to carry out data check and correction meets automatic Proofreading condition is as follows,
Medicine one's own department or unit code field and medicine this bit code memo field in terminal-pair medicine information record are identified, and judge medicine one's own department or unit
Whether the form of this bit code included in code field meets this bit code of standard form and judges to wrap in medicine this bit code memo field
Whether the form of this bit code remarks unit contained meets standard this bit code remarks form, when this bit code and this bit code remarks unit are equal
When meeting reference format requirement, judge whether the quantity of this bit code is equal with the quantity of this bit code remarks unit, when quantity is equal
When, terminal judges whether this bit code part included in medicine this bit code unit is consistent with this bit code, when this bit code is consistent,
Medicine information record meets automatic Proofreading condition, terminal can by this bit code of medicine memo field is carried out automatic parsing come pair
Specs field and formulation field are proofreaded.
Wherein, in above-mentioned deterministic process when there is either step to be unsatisfactory for Rule of judgment, i.e. this bit code or this bit code is standby
Note unit be unsatisfactory for reference format requirement, or meet reference format requirement this bit code and this bit code remarks unit quantity not
It is equal, when quantity is equal but this bit code is inconsistent, show that this bit code information is imperfect, medicine this bit code memo field cannot function as
The foundation proofreaded to specification and formulation, the medicine information for being unsatisfactory for automatic Proofreading condition record is transferred to artificial check and correction collection
Close, the specification and dose-form information recorded by auditor to the medicine information of artificial check and correction set is audited and corrected.
Step 140, when medicine information record meets automatic Proofreading condition, remembered according to default extracting rule from medicine information
Specification data and formulation data are extracted in medicine this bit code memo field in record.
The specification of medicine refer to by every, often in the pharmaceutical preparation in units of bag or every etc. contained active ingredient amount,
Measurement unit information and quantity information are included in specification data, as specification for " in every weight 0.23g " comprising measurement unit " g " and
Quantity information " 0.23 ".The formulation of medicine refers in order to treat needs and easy to use, by the powder, liquid or semisolid of medicine
The form of various trait, such as tablet, granule, capsule, injection, ointment is made in raw material, and agent is included in formulation data
Type type keyword.
Default extracting rule refers to extraction specification data and the agent from medicine this bit code memo field that terminal is pre-set
The rule of type data.The rule split to medicine this bit code memo field is specifically included, according to measurement unit, quantity information
Or types of formulation keyword judges the rule of the data type (belonging to specification data or formulation data) of the data after splitting,
And how will determine that the data after the fractionation of data type are extracted as the rules of specification data and formulation data.Terminal is according to pre-
If extracting rule is split the remarks section in medicine this bit code memo field, the data type of the data after splitting is judged
Formulation or specification, terminal by data type be formulation fractionation after data be extracted as formulation data, be rule by data type
Data are extracted as specification data after the fractionation of lattice.
Step 150, specs field and formulation field in being recorded according to specification data and formulation data to medicine information enter
Row is proofreaded and generates collation, and operation corresponding with collation is carried out to medicine information record.
Specs field during the specification data extracted is recorded with medicine information is compared, the formulation number that will be extracted
According to generation collation is compared with formulation field, collation passes through including check and correction and two kinds of situations of data exception, for
Proofread the medicine information record passed through to be retained, recorded for the medicine information of data exception, according to specific variance data
Comparison result is sorted out to its abnormal problem, and is operated accordingly according to specific abnormal problem type.Specifically, example
Such as, when the situation of content vacancy or missing occurs in specs field, specs field can be supplemented according to specification data；Work as agent
When type-word section difference occurs with formulation data content, abnormal problem is labeled as formulation problem and marks out variance data, by this
Medicine information record is sent to auditor and audited.
Basic drug information proofreading method in the present embodiment, by judging whether medicine information record needs to proofread, and
Whether the medicine information record for judging to need to carry out data check and correction meets automatic Proofreading condition, and qualified medicine information is remembered
This bit code of medicine memo field in record carries out automatically extracting for specification data and formulation data, and root according to default extracting rule
Specs field and formulation field in being recorded according to the data after extraction to medicine information are proofreaded, to medicine after generation collation
Product data carry out respective handling, so as to realize the automatic business processing of medicine information check and correction process, without manually remembering to medicine information
Record is audited one by one, is saved manpower and proof time, is effectively increased correction efficiency, while avoid due to artificial origin
Caused by leakage examine or the situation of examination ＆ verification mistake, improve the accuracy rate of proof-reading.
In one embodiment, step 130 specifically includes following steps：
In medicine one's own department or unit code field includes in identification medicine information record this bit code and medicine this bit code memo field
This bit code remarks unit.
When specification, formulation when medicine be not unique, multiple bit codes are included in the code field of medicine one's own department or unit, this bit code of medicine is standby
Note and multiple bit code remarks units are included in field, typically pass through between multiple bit codes, between multiple bit code remarks units
Separator such as branch, space etc. are separated, in the code field of medicine one's own department or unit by separator before, between two separators or point
Character recognition after symbol is this bit code, with same method by multiple bit codes in medicine this bit code memo field
Remarks unit identifies respectively.
Format check is carried out to this bit code and this bit code remarks unit.
This bit code is made up of 14 continuous pure digi-tals and middle no any interval, and this bit code remarks unit is by one's own department or unit
Code part and remarks section two parts composition, this bit code part and this bit code are completely the same, and the form of remarks section is standby for a pair
Remarks content in note symbol and remarks symbol, remarks symbol be " [] ", preceding remarks symbol " between [" and this bit code part continuously, not between
Every.
For example, authentication code is " Chinese medicines quasi-word Z22020105 " Xiao Ke Lin piece has two groups of specifications, formulation " every weight
0.36g (plain piece) " and " every weight 0.37g (Film coated tablets) ", correspond to respectively two this bit codes " 86903375000289 ",
" 86903375000302 " and two this bit code remarks units " 86903375000289 [every weight 0.36g (plain piece)] ",
" 86903375000302 [every weight 0.37g (Film coated tablets)] ", it can be seen that in each this bit code remarks unit remarks symbol
Content it is corresponding with one group of specification, formulation.
When to one's own department or unit code check, whether the number of characters for judging this bit code is 14, if so, judging whether 14 characters are complete
It is numeral entirely, if so, then judging that one's own department or unit code symbol closes preset standard form.In one embodiment, judging that it is pre- that one's own department or unit code symbol is closed
It is marked with after quasiconfiguaration, further verification is carried out to this bit code and is calculated, judges the accuracy of this bit code.Specifically, this bit code
Last position is check code, and by 13 bit digitals before this bit code, according to national standard, " GB 18937 " computational methods are calculated
Obtained result judges whether unanimously, if unanimously, judging that this bit code is correct, if inconsistent, to sentence compared with check code
This fixed bit code is abnormal.When this bit code does not meet preset format or this bit code exception, corresponding medicine information is recorded into line number
According to abnormal mark, and it is transferred to abnormal data set and is audited by auditor, obtains the deletion instruction or modification of auditor
After instruction, medicine information record is deleted or modified.
When being verified to this bit code remarks unit, whether all characters for judging this bit code remarks unit are 14 digits
Whether word, 14 bit digitals accord with comprising one group of remarks afterwards, and whether remarks symbol is connected with last 14 bit digital before judgement, works as one's own department or unit
When code remarks unit fully meets above-mentioned Rule of judgment, this bit code remarks unit meets preset standard form, when this bit code remarks
When unit does not meet preset standard form, corresponding medicine information record is transferred to artificial check and correction set, by auditor to people
The specification and dose-form information of the medicine information record of work check and correction set are audited and corrected.
When the form of this bit code and the form of this bit code remarks unit meet preset format, the quantity of this bit code is judged
It is whether equal with the quantity of this bit code remarks unit and be all higher than 1；If so, medicine information record meets automatic Proofreading condition.
When the form of this bit code and this bit code remarks unit meets preset format, quantity and one's own department or unit of this bit code are judged
Whether the quantity of code remarks unit is all higher than 1, when quantity is all higher than 1, judges the quantity of this bit code and this bit code remarks unit
It is whether equal, when quantity is equal, judges that medicine information record meets automatic Proofreading condition, this bit code remarks unit can be passed through
Specs field and formulation field are audited.When the quantity of this bit code and this bit code remarks unit is unsatisfactory for above-mentioned condition,
Corresponding medicine information record is transferred to artificial check and correction set.
Further, after judging that this bit code is equal with the quantity of this bit code remarks unit, by this bit code remarks unit
In this bit code part matched with this bit code, judge whether both correspond, when this bit code Incomplete matching being present
During situation, corresponding medicine information record progress this bit code abnormal problem is marked and is transferred to abnormal data set.
In the present embodiment, by being verified to the form of this bit code and this bit code remarks unit, and its quantity is entered
Row compares, it can be found that the data of this bit code Information abnormity.And it can filter out with multiple bit codes i.e. specification, formulation data
It is more complicated, it is necessary to carry out emphasis examination ＆ verification to specification, formulation problem, and this bit code information also complies with the medicine of automatic Proofreading condition
Information record, screening, the working time of verifying work can be effectively reduced, and improve the standard of this bit code information format verification examination ＆ verification
True property.
In one embodiment, step 140 specifically includes following steps：
Medicine this bit code memo field is split as multiple bit code remarks units.
When medicine information record meets automatic Proofreading condition, identify that separator is as divided in medicine this bit code memo field
Number, space etc., using separator as separation, by before first separator, after last separator and two separations
Character between symbol is extracted as this bit code remarks unit respectively.For example, " Chinese medicines quasi-word Z22020105's " disappears authentication code
This bit code of medicine memo field in thirsty clever piece medicine information record is " 86903375000289 [every weight 0.36g (plain piece)]；
86903375000302 [every weight 0.37g (Film coated tablets)] ", separator in field for one "；", therefore, by field from
“；" place disconnects, be split as two this bit code remarks units " 86903375000289 [every weight 0.36g (plain piece)] " and
" 86903375000302 [every weight 0.37g (Film coated tablets)] ".
Extract the remarks data in this bit code remarks unit.
Identify in this bit code remarks unit remarks symbol " [] ", by remarks accord with character be extracted as remarks data, such as
" every weight 0.36g (plain piece) " in " 86903375000289 [every weight 0.36g (plain piece)] " is extracted as remarks data.
Identify the extraction identifier in remarks data.
It is without specific semantic symbol in remarks data to extract identifier, it is generally the case that before and after extraction identifier
Content be respectively provided with independent semanteme, therefore, can according to extraction identifier by remarks data carry out content fractionation.Terminal recognition is standby
Whether note in data comprising extraction identifier.
Extraction identifier includes separator and the class of bracket two.Separator include space, ", ", "：" and "；" etc., for example, standby
Data are noted as " sugar coated tablet plate core weight 0.4g ", the separator in remarks data be space, and the data before and after space all have independence
Semanteme, " sugar coated tablet " represent medicine formulation, " plate core weight 0.4g " represent medicine specification.Bracket is one group or two groups
" () ", bracket is inside and outside or two brackets between data also all there is independent semanteme, for example, remarks data are " tablet is (sugared
Clothing) ", " tablet " represents the formulation of medicine, and " sugar-coat " also illustrates that formulation, is the further explanation to formulation.Therefore, there is separator
The content separated with bracket wherein some may represent formulation, the expression specification that has, it is also possible to represent formulation, or equal table
Show specification.
Remarks data are split according to extraction identifier.
Terminal identifies in remarks data whether there is separator first, when having separator in remarks data, to separate
Accord with and remarks data are divided into two parts for boundary, i.e., by the data before separator in remarks data and the data after separator
Split out respectively.
When there is no separator in remarks data, whether there is bracket in terminal recognition remarks data, have when in remarks data
When having bracket, remarks data are divided as boundary using left-hand bracket and unquote, i.e., by remarks data within a pair of brackets, it
Outer data split out respectively.
It should be noted that when terminal recognition goes out and has separator in remarks data, without identifying again according to separator
Whether there is bracket in data after being split, that is, also do not torn open when there is bracket in the data after splitting further according to bracket
Point.
Judge the data type of the remarks data after splitting.
Data type is divided into two classes, is specification data and formulation data respectively.In one embodiment, judge after splitting
The step of data type of remarks data, specifically includes：Judge whether include specification character in the remarks data after splitting, when tearing open
When including specification character in the remarks data after point, the data type of the remarks data after fractionation is specification；It is standby after fractionation
When not including specification character in note data, the data type of the remarks data after fractionation is formulation.
Specifically, specification character is Arabic numerals and the measurement unit for referring to be identified metered amounts, such as
" 0.35g ", " 0.7 milligram " etc..Preferably, when terminal identifies Arabic numerals from the remarks data after fractionation i.e. by this
Data markers are specification；By this data markers it is formulation when terminal does not recognize Arabic numerals.
Obtain it is corresponding with extraction identifier presets extracting rule, according to default extracting rule and data type from this bit code
Specification data and formulation data are extracted in remarks unit.
When it is separator to extract identifier, the first default extracting rule is obtained.The judged result of remarks data after fractionation
It is divided into four kinds of situations：1st, the data before and after separator are specification；2nd, the data before and after separator are formulation；3rd, separator
Preceding data are that the data after specification, separator are formulation；4th, the data before separator are that the data after formulation, separator are rule
Lattice.First default extracting rule is when terminal judges that it is situation 1 or situation 2 to split data result, and whole memo field is carried
Specification or formulation are taken as, when terminal judges to split data result as situation 3 or situation 4, by the field after fractionation according to judgement
As a result specification or formulation are accordingly extracted as.
Extraction identifier is divided into three major types for the remarks data of bracket：The first kind, one group of bracket, there are data before bracket
There are data " (* *) * * " after " * * (* *) " or bracket；Second class, one group of bracket, there are data " * * (* *) * * " before and after bracket；The
Three classes, two groups of brackets " * * (* *) * * (* *) ".
When it is the first kind to extract identifier, the second default extracting rule is obtained.For primary sources, remarks after fractionation
The judged result of data is similar for the situation of separator with extraction identifier：1st, the data inside and outside bracket are specification；2nd, bracket
Inside and outside data are formulation；3rd, the data in bracket be specification, the data outside bracket be formulation；4th, the data outside bracket are agent
Data in type, bracket are specification.Second default extracting rule is when terminal judges that it is situation 1 or situation 2 to split data result
When, whole memo field is extracted as specification data or formulation, when terminal judges to split data result as situation 3 or situation 4,
Field after fractionation is accordingly extracted as specification data or formulation according to result of determination.
When it is the second class to extract identifier, the 3rd default extracting rule is obtained.For secondary sources, remarks after fractionation
The byte orderings of data share 8 kinds of situations：1st, specification (specification) specification；2nd, specification (specification) formulation；3rd, specification (formulation) specification；
4th, specification (formulation) formulation；5th, formulation (specification) specification；6th, formulation (specification) formulation；7th, formulation (formulation) specification；8th, formulation (agent
Type) formulation.3rd default extracting rule is when terminal judges that it is situation 1 or situation 3 to split data result, by whole remarks word
Section is extracted as specification data；When terminal judges to split data result as situation 2, by before bracket with the data in bracket together with including
Number specification data is extracted as, the data after bracket are extracted as formulation data；When terminal judges to split data result for situation 4
When, the data before bracket are extracted as specification data, the data in bracket and after bracket are extracted as formulation data together with bracket；
When terminal judges to split data result as situation 5 or situation 6, the data before bracket are extracted as formulation data, bracket neutralizes
Data after bracket are extracted as specification data together with bracket；When terminal judge split data result for situation 7 when, by before bracket with
Data in bracket are extracted as formulation data together with bracket, and the data after bracket are extracted as into specification data；When terminal judges to tear open
When divided data result is situation 8, whole memo field is extracted as formulation data.
When it is three classes to extract identifier, the 4th default extracting rule is obtained.For the 3rd class data, remarks after fractionation
The byte orderings that data are likely to occur share 4 kinds of situations：1st, specification (specification) formulation (formulation)；2nd, formulation (formulation) specification (rule
Lattice)；3rd, specification (specification) specification (formulation)；4th, formulation (formulation) formulation (specification).When terminal judges to split data result for feelings
During condition 1, the first two fractionation data are extracted as specification data together with bracket, latter two splits data and is extracted as formulation together with bracket
Data；When terminal judges to split data result as situation 2, the first two fractionation data are extracted as formulation data together with bracket,
Latter two splits data and is extracted as specification data together with bracket；When terminal judges to split data result as situation 3, by first three
Split data and be extracted as specification data together with bracket, last splits data and is extracted as formulation data；When terminal judges to split
When data result is situation 4, first three fractionation data is extracted as formulation data together with bracket, last splits data extraction
For specification data.
Further, in one embodiment, when in remarks data without extraction identifier when, judge be in remarks data
It is no to include specification character, when including specification character in remarks data, remarks data are extracted as specification data；When remarks data
In when not including specification character, remarks data are extracted as formulation data.
When terminal had not both identified separator not from remarks data or do not identified bracket, not to remarks number
According to being split, whether there is above-mentioned specification character in terminal Direct Recognition remarks data, judge when with specification character standby
Note data are specification data, and remarks data are directly extracted as into specification data, otherwise are extracted as formulation data.
In the present embodiment, by being split remarks data automatically according to extraction identifier, after identifying fractionation
Specification character in data judges to split the data type of data, then the data that by data type will be judged, according to remarks
Extracting rule is preset corresponding to data type to automatically extract as specification data and formulation data, can be to Various Complex situation
The specifications of remarks data, formulation rapidly, fully automatically parse, following data proof-reading has been carried out sufficiently
Preparation, further improve the efficiency of proof-reading.
In one embodiment, step 150 specifically includes following steps：
Specification data and specs field are subjected to consistency desired result and obtain specification check results.
The consistency desired result of specification refers to by specification data compared with specs field, judges specification data and specification word
Whether effective specification information with The concrete specification implication in section is consistent, when both effective specification informations are consistent, specification
Check results are that successfully, when effective specification information is inconsistent, specification check results are abnormal.
Formulation data and formulation field are subjected to consistency desired result and obtain formulation check results.
The consistency desired result of formulation refers to formulation data compared with formulation field, judges formulation data and formulation word
Whether the effective dosage forms information with specific formulation implication in section is consistent, when both effective dosage forms information is consistent, formulation
Check results are that successfully, when effective dosage forms information is inconsistent, formulation check results are abnormal.
Specification problem mark is carried out for abnormal medicine information record to specification check results, is different to formulation check results
Normal medicine information record carries out formulation problem mark.
When the specs field in medicine information record and the check results of formulation field are abnormal, terminal-pair medicine letter
Breath record carries out specification problem mark and memory problem mark simultaneously.
The medicine information for being labeled with specification problem and/or formulation problem record is sent to auditor.
Above-mentioned specification, formulation data proof-reading after the completion of, when medicine information record is labeled with specification problem, or mark
When having formulation problem, or being labeled with specification problem and formulation problem simultaneously, medicine information record is sent to auditor
Audited.In one embodiment, the medicine information record of carry out problem mark is transferred to abnormal data set by terminal, treats institute
After the completion of the medicine information record check and correction in need for carrying out data check and correction, abnormal data set is sent into an auditor and examined
Core.In one embodiment, the medicine information marked with problem record or abnormal data set are being sent to person approving
During member, will have discrepant specification information and specification information and carry out contrasting display or carry out highlighted mark, and be easy to auditor to enter
Row is verified.
In the present embodiment, by the way that specification data and specs field, formulation data and formulation field are carried out into automatic Verification,
The medicine information record of data exception can be quickly found out, and by being sent after medicine information is recorded into carry out problem mark
To auditor, facilitate auditor to determine abnormal data source, improve review efficiency.
In one embodiment, specification data and specs field are subjected to consistency desired result and obtain the step of specification check results
Suddenly specifically include：Specs field is split as specification unit, judge the quantity of specification unit and specification data quantity whether phase
Deng.If unequal, specification exception check results are generated；If equal, specification data is matched one by one with specification unit, when not
During in the presence of the specification unit to match with specification data, specification exception check results are generated.
Formulation data are carried out into the step of consistency desired result obtains formulation check results with formulation field to specifically include：By agent
Type-word section is split as dosage form units, judges whether the quantity of dosage form units is equal with the quantity of formulation data；If unequal, generation
Formulation exception check results；If equal, from formulation extracting data formulation keyword, formulation keyword and dosage form units are carried out
Match one by one, when in the absence of the dosage form units to match with formulation keyword, generate formulation exception check results.
Specifically, specification unit is represents a kind of character string of specification, dosage form units are a kind of character string of formulation of expression.
When the medicine of same authentication code has multiple bit codes, the specification list that should include in the specs field in medicine information record
Member quantity and dosage form units quantity at least one be multiple and quantity it is identical with the quantity of this bit code.
When specification data and specs field are carried out consistency desired result by terminal, whether included in terminal recognition specs field
Separator as "：", ", ", ", ", "/", "；”、“.", " and " or "or" etc., after terminal recognition goes out separator, terminal will divide
Split out to obtain multiple specification units respectively every the front and rear character string of symbol, when terminal does not recognize separator, without
Split, whole specs field is identified as a specification unit.By the quantity of specification unit and the quantity of the specification data extracted
It is compared, judges whether quantity is equal, if quantity, generates specification exception check results.If quantity is equal, by specification number
Matched one by one according to specification unit, the process of matching specifically includes：By in each specification data specification character (i.e. I
Uncle's numeral and measurement unit) extract, search whether the specification unit for including same size character be present, if in the presence of,
With success, if being not present, it fails to match.It is to generate specification unsuccessful verification result that when all specification datas, all the match is successful；When
As long as there is a specification data to generate specification exception check results when the match is successful.
When formulation data and formulation field are carried out consistency desired result by terminal, whether included in terminal recognition formulation field
Separator as "：", ", ", ", ", "/", "；”、“.", " and " or "or" etc., after terminal recognition goes out separator, terminal will divide
Split out to obtain multiple specification units respectively every the front and rear character string of symbol, when terminal does not recognize separator, terminal is known
Whether digital number such as " 1. ", " (1) " or " [1] " is included in other formulation field, when terminal recognition makes to digital number, by two
The character string after character string or last digital number between individual digital number splits out to obtain multiple dosage form units,
When terminal had not both recognized separator or do not recognized digital number, without splitting, whole formulation field is identified
For one dosage type low temperature unit.
By the quantity of dosage form units compared with the quantity of the formulation data extracted, judge whether quantity is equal, if
Quantity, generate formulation exception check results.If quantity is equal, the formulation keyword extraction in each formulation data is gone out
Come, formulation keyword is matched one by one with dosage form units.In one embodiment, terminal has been previously stored formulation keyword
Table, stored common formulation key character in formulation key table, such as " tablet ", " sugar-coat ", " film-coating ", " big honeyed bolus ",
" plain piece " etc..Terminal comes out the formulation keyword extraction in formulation data according to formulation key table, searches whether exist
The dosage form units of same dosage form keyword are completely included, when it is present, the match is successful；When in the absence of when, it fails to match.Another
In individual embodiment, for terminal without the extraction of formulation keyword, terminal calculates the phase of each formulation data and each dosage form units
Like degree, the computational methods of similarity can be the ratio of the two identical characters number and formulation data character number, when ratio exceedes in advance
If during threshold value (such as 85%), the match is successful；When ratio is less than predetermined threshold value, it fails to match.Specific predetermined threshold value can root
Summarize and be calculated according to the similarity of multiple data that the match is successful.
It is to generate formulation unsuccessful verification result that when all formulation data, all the match is successful；As long as when there is a formulation data
Formulation exception check results can not be generated when the match is successful.
In one embodiment, single this bit code of medicine only is included when terminal recognition goes out in medicine information record, be unsatisfactory for
, can also be by by judging the data type in medicine this bit code memo field, according to above-mentioned verification side during automatic Proofreading condition
Method is verified remarks data and specs field or formulation field, so as to also be capable of the medicine of single this bit code of medicine of automatic decision
Whether the data of product information record are abnormal.
In one embodiment, when specification and formulation check results are to verify successfully, during medicine information is recorded
Specs field and formulation field replace with the formulation data and specification data extracted in medicine this bit code remarks, and by formulation number
Corresponded according to, specification data with corresponding this bit code of medicine, be easy to user to check.Specifically, it is one as shown in Table 1
The information of medicine one's own department or unit code field, formulation field and specs field in bar medicine information record.
Table one：
As can be seen from Table I, specs field includes two specification units " per packed 2.5g " and " 90g ", but from table
One can not find out the two specification units specifically with which this bit code in two medicine this bit codes to corresponding.
As shown in Table 2, table two is knot of the medicine information record by specification, the check and correction of formulation data and amendment in table one
Fruit.This bit code of medicine memo field in medicine information record includes two this bit code remarks units altogether
" 86900286000858 [per packed 90g] " and " 86900286000841 [per packed 2.5g] ", this bit code remarks unit is entered
Result after the extraction of row data is to extract specification data " per packed 90g " and " per packed 2.5g ".By having in specification data
Specification information " 90g " is imitated " to carry out with " 90g " per packed 2.5g " with " 2.5g " and the specification unit in the specs field in table one
Matching, can the match is successful completely.Because not extracting formulation data, the number of the dosage form units in client checks formulation field
Measure for one when verify successfully.
Table two：
Terminal by specification data " per packed 90g " with its belonging to this bit code remarks unit in this bit code part
" 86900286000858 " are associated, and by specification data " per packed 2.5g " with its belonging to this bit code remarks unit in sheet
Bit code part " 86900286000841 " is associated, and the specs field in table one and medicine one's own department or unit code field is revised as above-mentioned
Specification data code data in one's own department or unit associated with it, finally give medicine information record correction result as shown in Table 2.
In the present embodiment, by being modified to check and correction field, user can be made when checking Basic drug information, energy
Enough become more apparent upon the related information between different field.
In one embodiment, as shown in Fig. 2 internal structure schematic diagram for a terminal.The terminal includes passing through
Processor, non-volatile memory medium and the built-in storage of bus of uniting connection.Wherein, the non-volatile memory medium storage of terminal
There are operating system and database, in addition to a kind of Basic drug information verifying unit.Database is used to be stored in realize a kind of medicine
The related data of product essential information proofreading method, including medicine information data of each version of storage etc., Basic drug information school
Device is used to realize a kind of Basic drug information proofreading method.The processor is used to provide calculating and control ability, and support is whole
The operation of individual terminal.Built-in storage in terminal is the operation of the Basic drug information verifying unit in non-volatile memory medium
Environment is provided, computer-readable instruction can be stored in the built-in storage, can when the computer-readable instruction is executed by processor
A kind of so that Basic drug information proofreading method of computing device.It will be understood by those skilled in the art that the knot shown in Fig. 1
The block diagram of structure, the only part-structure related to application scheme, do not form what application scheme was applied thereon
The restriction of terminal, specific terminal can include than more or less parts shown in figure, either combine some parts or
Arranged with different parts.
In one embodiment, as shown in Figure 3, there is provided a kind of Basic drug information verifying unit, the device include：
Data acquisition module 310, for obtaining latest edition medicine information data；
Identification module 320, for identifying the medicine information for needing to carry out data check and correction in latest edition medicine information data
Record；
Automatic Proofreading judge module 330, for identifying this bit code information in medicine information record, according to this bit code information
Judge whether medicine information record meets automatic Proofreading condition；
Extraction module 340, extracting rule is preset from medicine this bit code memo field in medicine information record for basis
Middle extraction specification data and formulation data；
Checking module 350, for the specs field in being recorded according to specification data and formulation data to medicine information and agent
Type-word section is proofreaded and generates collation, and operation corresponding with collation is carried out to medicine information record.
In one embodiment, as shown in figure 4, automatic Proofreading judge module 330 includes：
Unit identification module 332, for identifying this bit code for including of medicine one's own department or unit code field and medicine in medicine information record
This bit code remarks unit in product this bit code memo field；
Format check module 334, for carrying out format check to this bit code and this bit code remarks unit；
Quantity correction verification module 336, for meeting default lattice when the form of this bit code and the form of this bit code remarks unit
During formula, judge this bit code quantity and this bit code remarks unit quantity it is whether equal and be all higher than 1；If so, medicine information is remembered
Record satisfaction automatically extracts condition.
In one embodiment, as shown in figure 5, extraction module 340 includes：
Unit splits module 341, for medicine this bit code memo field to be split as into multiple bit code remarks units；
Remarks extraction module 342, for extracting the remarks data in this bit code remarks unit；
Identifier identification module 343, for identifying the extraction identifier in remarks data；
Data split module 344, for being split according to extraction identifier to remarks data；
Type judging module 345, for judging the data type of the remarks data after splitting；
Data extraction module 346, for obtaining default extracting rule corresponding with extracting identifier, advised according to default extraction
Then specification data and formulation data are extracted with data type from this bit code remarks unit.
In one embodiment, as shown in fig. 6, checking module 350 includes：
Specification correction verification module 352, specification verification knot is obtained for specification data and specs field to be carried out into consistency desired result
Fruit；
Formulation correction verification module 354, formulation verification knot is obtained for formulation data and formulation field to be carried out into consistency desired result
Fruit；
Problem labeling module 356, for carrying out specification problem mark to specification check results for abnormal medicine information record
Note, formulation problem mark is carried out for abnormal medicine information record to formulation check results；
Sending module 358, for the medicine information record for being labeled with specification problem and/or formulation problem to be sent into examination ＆ verification
Personnel.
One of ordinary skill in the art will appreciate that realize all or part of flow in above-described embodiment method, being can be with
Completed by the related hardware of computer program instructions, described program can be stored in a computer read/write memory medium
In, the program is upon execution, it may include such as the flow of the embodiment of above-mentioned each method.Wherein, described storage medium can be magnetic
Dish, CD, read-only memory (Read-Only Memory, ROM) or random access memory (RandomAccess
Memory, RAM) etc..
Each technical characteristic of embodiment described above can be combined arbitrarily, to make description succinct, not to above-mentioned reality
Apply all possible combination of each technical characteristic in example to be all described, as long as however, the combination of these technical characteristics is not deposited
In contradiction, the scope that this specification is recorded all is considered to be.
Embodiment described above only expresses the several embodiments of the present invention, and its description is more specific and detailed, but simultaneously
Can not therefore it be construed as limiting the scope of the patent.It should be pointed out that come for one of ordinary skill in the art
Say, without departing from the inventive concept of the premise, various modifications and improvements can be made, these belong to the protection of the present invention
Scope.Therefore, the protection domain of patent of the present invention should be determined by the appended claims.
Claims (10)
1. a kind of Basic drug information proofreading method, it is characterised in that the described method comprises the following steps：
Obtain latest edition medicine information data；
Identify the medicine information record for needing to carry out data check and correction in the latest edition medicine information data；
This bit code information in the medicine information record is identified, judges that the medicine information records according to described bit code information
Whether automatic Proofreading condition is met；
When medicine information record meets the automatic Proofreading condition, remembered according to default extracting rule from the medicine information
Specification data and formulation data are extracted in medicine this bit code memo field in record；
Specs field and formulation field in being recorded according to the specification data and the formulation data to the medicine information enter
Row is proofreaded and generates collation, and operation corresponding with the collation is carried out to medicine information record.
2. Basic drug information proofreading method according to claim 1, it is characterised in that the identification medicine information
This bit code information in record, judge whether the medicine information record meets automatic Proofreading condition according to described bit code information
The step of include：
Identify in this bit code and medicine this bit code memo field that medicine one's own department or unit code field includes in the medicine information record
This bit code remarks unit；
Format check is carried out to described bit code and described bit code remarks unit；
When the form of described bit code and the form of described bit code remarks unit meet preset format, described one's own department or unit is judged
Whether the quantity of code and the quantity of described bit code remarks unit are equal and be all higher than 1；If so, the medicine information record meets
Automatic Proofreading condition.
3. Basic drug information proofreading method according to claim 1, it is characterised in that the basis presets extracting rule
The step of extracting specification data and formulation data from medicine this bit code memo field in medicine information record includes：
Medicine this bit code memo field is split as multiple bit code remarks units；
Extract the remarks data in described bit code remarks unit；
Identify the extraction identifier in the remarks data；
The remarks data are split according to the extraction identifier；
Judge the data type of the remarks data after splitting；
Default extracting rule corresponding with the extraction identifier is obtained, according to the default extracting rule and the data type
The specification data and the formulation data are extracted from described bit code remarks unit.
4. Basic drug information proofreading method according to claim 3, it is characterised in that methods described also includes：
When in the remarks data without extraction identifier, judge whether include specification character in the remarks data, work as institute
State when specification character is included in remarks data, the remarks data are extracted as specification data；Do not wrapped when in the remarks data
During character containing specification, the remarks data are extracted as formulation data；
The step of data type of the remarks data after the judgement fractionation, includes：
Judge whether include specification character in the remarks data after splitting；
When including the specification character in the remarks data after fractionation, the data type of the remarks data after fractionation
For specification；When not including the specification character in the remarks data after fractionation, the number of the remarks data after fractionation
It is formulation according to type.
5. Basic drug information proofreading method according to claim 1, it is characterised in that described according to the specification data
Specs field and formulation field in being recorded with the formulation data to the medicine information are proofreaded and generate collation,
The step of carrying out operation corresponding with the collation to medicine information record includes：
The specification data and the specs field are subjected to consistency desired result and obtain specification check results；
The formulation data and the formulation field are subjected to consistency desired result and obtain formulation check results；
Specification problem mark is carried out for abnormal medicine information record to the specification check results, to the formulation check results
Formulation problem mark is carried out for the medicine information record of exception；
The medicine information for being labeled with specification problem and/or formulation problem record is sent to auditor.
6. Basic drug information proofreading method according to claim 5, it is characterised in that it is described by the specification data with
The step of specs field progress consistency desired result obtains specification check results includes：
The specs field is split as specification unit, judge the quantity of specification unit and the specification data quantity whether phase
Deng；
If unequal, specification exception check results are generated；If equal, the specification data and the specification unit are carried out one by one
Matching, when in the absence of the specification unit to match with the specification data, generate specification exception check results；
The described the step of formulation data are obtained into formulation check results with formulation field progress consistency desired result, includes：
The formulation field is split as dosage form units, judge the quantity of dosage form units and the formulation data quantity whether phase
Deng；
If unequal, formulation exception check results are generated；If equal, from the formulation extracting data formulation keyword, by institute
State formulation keyword to be matched one by one with the dosage form units, when in the absence of the formulation list to match with the formulation keyword
When first, formulation exception check results are generated.
7. a kind of Basic drug information verifying unit, it is characterised in that described device includes：
Data acquisition module, for obtaining latest edition medicine information data；
Identification module, for identifying the medicine information note for needing to carry out data check and correction in the latest edition medicine information data
Record；
Automatic Proofreading judge module, for identifying this bit code information in the medicine information record, believed according to described bit code
Breath judges whether the medicine information record meets automatic Proofreading condition；
Extraction module, for being carried according to default extracting rule from medicine this bit code memo field in medicine information record
Take specification data and formulation data；
Checking module, for the specs field in being recorded according to the specification data and the formulation data to the medicine information
Proofreaded with formulation field and generate collation, behaviour corresponding with the collation is carried out to medicine information record
Make.
8. Basic drug information verifying unit according to claim 7, it is characterised in that the automatic Proofreading judge module
Including：
Unit identification module, for identifying medicine one's own department or unit code field includes in medicine information record this bit code and medicine sheet
This bit code remarks unit in bit code memo field；
Format check module, for carrying out format check to described bit code and described bit code remarks unit；
Quantity correction verification module, for meeting default lattice when the form of described bit code and the form of described bit code remarks unit
During formula, judge described bit code quantity and described bit code remarks unit quantity it is whether equal and be all higher than 1；If so, institute
State medicine information record satisfaction and automatically extract condition.
9. Basic drug information verifying unit according to claim 7, it is characterised in that the extraction module includes：
Unit splits module, for medicine this bit code memo field to be split as into multiple bit code remarks units；
Remarks extraction module, for extracting the remarks data in described bit code remarks unit；
Identifier identification module, for identifying the extraction identifier in the remarks data；
Data split module, for being split according to the extraction identifier to the remarks data；
Type judging module, for judging the data type of the remarks data after splitting；
Data extraction module, for obtaining default extracting rule corresponding with the extraction identifier, according to the default extraction
Regular and described data type extracts the specification data and the formulation data from described bit code remarks unit.
10. Basic drug information verifying unit according to claim 7, it is characterised in that the checking module includes：
Specification correction verification module, specification verification knot is obtained for the specification data and the specs field to be carried out into consistency desired result
Fruit；
Formulation correction verification module, formulation verification knot is obtained for the formulation data and the formulation field to be carried out into consistency desired result
Fruit；
Problem labeling module, for carrying out specification problem mark to the specification check results for abnormal medicine information record,
Formulation problem mark is carried out for abnormal medicine information record to the formulation check results；
Sending module, for the medicine information record for being labeled with specification problem and/or formulation problem to be sent into person approving
Member.
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| CN113361254A (en) * | 2021-06-03 | 2021-09-07 | 重庆南鹏人工智能科技研究院有限公司 | Automatic electronic medical record analysis method and device |
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