CN114757613A - Intelligent management system for storing finished goods in medical instrument production and sales warehouse - Google Patents
Intelligent management system for storing finished goods in medical instrument production and sales warehouse Download PDFInfo
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- 238000004519 manufacturing process Methods 0.000 title claims abstract description 50
- 238000003860 storage Methods 0.000 claims abstract description 55
- 230000001954 sterilising effect Effects 0.000 claims abstract description 52
- 238000004659 sterilization and disinfection Methods 0.000 claims abstract description 52
- 230000000694 effects Effects 0.000 claims abstract description 40
- 238000007789 sealing Methods 0.000 claims abstract description 36
- 230000014759 maintenance of location Effects 0.000 claims abstract description 31
- 238000012216 screening Methods 0.000 claims abstract description 25
- 238000012856 packing Methods 0.000 claims abstract description 9
- 238000004458 analytical method Methods 0.000 claims description 32
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- 238000004806 packaging method and process Methods 0.000 claims description 17
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- 230000001580 bacterial effect Effects 0.000 claims description 10
- 230000036512 infertility Effects 0.000 claims description 10
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- 238000000034 method Methods 0.000 claims description 3
- 230000003287 optical effect Effects 0.000 claims description 3
- 208000035143 Bacterial infection Diseases 0.000 description 3
- 208000022362 bacterial infectious disease Diseases 0.000 description 3
- 238000006467 substitution reaction Methods 0.000 description 3
- 241000894006 Bacteria Species 0.000 description 2
- 238000009826 distribution Methods 0.000 description 2
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- 230000009286 beneficial effect Effects 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
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Abstract
The invention relates to the field of medical instrument storage management, in particular to a commodity finished product storage intelligent management system of a medical instrument production and sales warehouse, which comprises the steps of screening various sterile medical instruments with the packing sealing performance in various types to be put into the warehouse, analyzing the surface colony area ratio, the sterile package dryness and the remaining sterilization effect retention time of the sterile medical instruments in various types, calculating the comprehensive quality influence coefficient of the sterile medical instruments in various types to be put into the warehouse, comparing and screening the qualified sterile medical instruments in various types to be put into the warehouse, obtaining the effective period duration of the qualified sterile medical instruments in various types to be put into the corresponding type sterile medical instrument storage area in the warehouse according to the sequence from short to long effective period, thereby effectively avoiding the failure phenomenon of the sterile medical instruments, the medical use safety of the aseptic medical instrument is improved, and the health of people using the aseptic medical instrument is guaranteed.
Description
Technical Field
The invention relates to the field of medical instrument storage management, in particular to an intelligent commodity finished product storage management system for a medical instrument production and sales warehouse.
Background
Domestic sterile medical instrument production enterprises can basically meet the requirements of domestic markets in terms of product types and production scales, but have the problem of hysteresis in terms of storage and management of finished sterile medical instruments, and bring risks to the health and medical safety of the masses.
At present, the existing aseptic medical instrument finished product storage management method has the following defects: 1. the existing storage management mode of the finished sterile medical instrument basically adopts manual management, namely manual pressure application is carried out manually to detect the sealing integrity of the sterile medical instrument package, so that the problems of low detection efficiency and low accuracy exist, the sterile medical instrument is subjected to bacterial infection, and the safety use performance of the sterile medical instrument is seriously influenced.
2. The existing sterile medical instrument finished product storage management mode only analyzes the quality of a corresponding instrument according to the sterilization time of the sterile medical instrument, and cannot analyze the quality safety of the sterile medical instrument according to various factors, so that the accuracy and the reliability of quality analysis of the sterile medical instrument are reduced, risks are brought to the health of people using the sterile medical instrument, and the medical use safety of the sterile medical instrument is reduced.
In order to solve the problems, an intelligent management system for storing finished goods in a medical instrument production and sales warehouse is designed.
Disclosure of Invention
The invention mainly aims to provide an intelligent management system for storing finished goods in a medical instrument production and sales warehouse, which solves the problems in the background technology.
In order to achieve the purpose, the invention provides an intelligent commodity product storage management system for a medical instrument production and sale warehouse, which comprises a sterile medical instrument classification module, a package tightness conformity screening module, a medical instrument parameter detection module, a medical instrument parameter analysis module, a sterilization effect retention time acquisition module, a sterile medical instrument quality analysis module, a medical instrument validity period acquisition module, a sterile medical instrument storage management module and a storage database.
The package tightness conformity screening module is used for screening various sterile medical instruments to be fed into the medical instrument production and sale warehouse, and the package tightness conformity screening module comprises the following specific screening steps: s11, by checking the integrity of the seal of each sterile medical device package of each type to be entered into the medical device manufacturing and distribution warehouse.
S12, comparing the seal integrity of each sterile medical device package of each type to be entered into the warehouse with the set package seal integrity.
And S13, if the sealing integrity of the package of the sterile medical appliance in a certain type to be put into the warehouse is more than or equal to the set sealing integrity of the package, indicating that the package of the sterile medical appliance in the certain type is in accordance with the sealing integrity.
S14, screening and counting each aseptic medical apparatus with the packing sealing performance in each type in the warehouse, recording each aseptic medical apparatus with the packing sealing performance as each aseptic medical apparatus with the packing sealing performance, and marking the serial number of each aseptic medical apparatus with the packing sealing performance as AicrWherein r is 1, 2.
The medical instrument parameter detection module is used for detecting relevant parameters which accord with sterile medical instruments in various types to enter the warehouse, and the detection steps are as follows: and S21, respectively carrying out optical scanning on the surfaces of the medical instruments conforming to the sterility in each type to be stored in the warehouse, and acquiring surface gray level images of the medical instruments conforming to the sterility in each type to be stored in the warehouse.
S22, extracting the surface bacterial colony area of each sterile medical instrument in each type to be stored in the warehouse, and marking the surface bacterial colony area of each sterile medical instrument in each type to be stored in the warehouse as Sicr。
S23, detecting the weight of each sterile medical appliance in each type to be put into the warehouse, and marking the weight of each sterile medical appliance in each type to be put into the warehouse as g icr。
The medical instrument parameter analysis module is used for analyzing relevant parameters which accord with sterile medical instruments in various types to enter the warehouse, and the specific analysis steps are as follows: and S31, extracting the standard surface area of each type of sterile medical instrument stored in the storage database, and analyzing the surface colony area ratio of each type of sterile medical instrument to be stored in the warehouse.
And S32, extracting the standard package weight and the standard sterile package weight of each type of sterile medical instrument stored in the storage database, and analyzing the dryness of each sterile package meeting the sterile medical instrument in each type to be stored in the warehouse.
The sterilization effect retention time acquisition module is used for acquiring each type of the bacteria to be stored in the warehouseThe method accords with the remaining sterilization effect maintaining time of the sterile medical apparatus, and comprises the following specific steps: s41, obtaining the packaging information of each sterile medical apparatus in each type in the warehouse, extracting the sterilization time of each sterile medical apparatus in each type in the warehouse, and marking the sterilization time of each sterile medical apparatus in each type in the warehouse as ticr。
And S42, extracting the standard sterilization effect holding time of each type of sterile medical instrument stored in the storage database, and analyzing the remaining sterilization effect holding time of each type of sterile medical instrument to be stored in the warehouse, wherein the remaining sterilization effect holding time meets the requirements of the sterile medical instrument.
The sterile medical apparatus quality analysis module is used for calculating comprehensive quality influence coefficients of various types of sterile medical apparatuses to be stored in the warehouse, and comparing and counting the qualified sterile medical apparatuses in the various types of sterile medical apparatuses to be stored in the warehouse.
As a further improvement of the invention, the sterile medical apparatus classification module is used for acquiring the commodity names corresponding to each sterile medical apparatus to enter the medical apparatus production and sales warehouse, comparing and analyzing the commodity types corresponding to each sterile medical apparatus to enter the medical apparatus production and sales warehouse, counting each sterile medical apparatus in each type to enter the medical apparatus production and sales warehouse, numbering each sterile medical apparatus in each type to enter the medical apparatus production and sales warehouse, and forming a sterile medical apparatus number set A in each type to enter the medical apparatus production and sales warehouseib＝{Aib1，Aib2，...，Aibj，...，Aibm}，AibjDenoted as the jth sterile medical instrument number of the ith type to be entered into the medical instrument production and sales warehouse, where i ═ 1, 2.
As a further improvement of the present invention, the package tightness conformity screening module further includes a step of counting each sterile medical instrument with non-conforming package tightness in each type to be put into the warehouse and placing the sterile medical instrument in an unqualified commodity area in the warehouse if the sealing integrity of the package of a certain type of sterile medical instrument to be put into the warehouse is less than the set package sealing integrity, which indicates that the packaging tightness of the sterile medical instrument in the type is not qualified.
As a further improvement of the present invention, the medical instrument parameter analysis module is used for analyzing the surface colony area ratio of each type of sterile medical instruments to be put into the warehouse, and comprises: the surface colony area s of each type of sterile medical instruments to be put into the warehouseicrSubstituting into formula
Obtaining the area ratio k of the surface bacterial colony conforming to each sterile medical instrument in each type to be put into the warehouseicrIn which S isSignAiExpressed as the standard surface area of the i-th type of sterile medical instrument.
As a further improvement of the present invention, the medical device parameter analysis module is used for analyzing the dryness of each sterile pack of each type conforming to a sterile medical device to be put into a warehouse, and comprises: the weight g of each package conforming to the sterile medical device in each type to be put into the warehouseicrSubstitution formula
Obtaining the dryness theta of each sterile pack which accords with the sterile medical instruments in each type to be put into the warehouseicrWhere μ is expressed as a correction factor for the dryness of the sterile package in the packaging of the medical device, gSign boardAiExpressed as the standard packaging weight, G ', of the ith type of sterile medical device'Sign boardExpressed as the standard sterile package weight in the medical device package.
As a further improvement of the present invention, the sterilization effect retention time acquisition module is configured to analyze remaining sterilization effect retention time of each of types of medical instruments conforming to sterility to be put into a warehouse, and includes: the sterilization time t of each type of medical instruments meeting the requirement of sterility in each type to be put into the warehouse icrSubstituting into formula t'icr＝TSign boardAi-(tReal time-ticr) Obtaining the remaining sterilization effect retention time t 'of each type of medical instruments meeting the sterility in the warehouse'icrWherein T isSign boardAiExpressed as the standard sterilization effect retention time, t, for the ith type of sterile medical instrumentReal timeIndicated as the current real time.
As a further improvement of the invention, the calculation formula of the comprehensive quality influence coefficient of each sterile medical instrument in each type to be put into the warehouse is
ξicrExpressed as the combined quality impact coefficient, λ, of the ith compliant sterile medical instrument of the ith type to be entered into the warehousek、λθ、λtRespectively expressed as the mass influence weight coefficient, k, of the surface colony area ratio, the dryness of the sterile package, and the remaining sterilization effect retention time of the sterile medical instrumenticrExpressed as the surface colony area ratio, theta, of the ith type to be entered into the warehouse in conformity with the sterile medical instrumenticrIs expressed as the dryness, t 'of the sterile pack of the ith conforming sterile medical instrument of the ith type to be entered into the warehouse'icrExpressed as the remaining sterilization effect retention time of the ith compliant sterile medical instrument of the ith type to be entered into the warehouse.
As a further improvement of the present invention, the sterile medical instrument quality analysis module is used for comparatively counting each qualified sterile medical instrument of each type to be put into the warehouse, and includes: comparing the comprehensive quality influence coefficient of each sterile medical instrument in each type to be stored in the warehouse with a set quality influence coefficient threshold, if the comprehensive quality influence coefficient of a certain sterile medical instrument in a certain type is smaller than the set quality influence coefficient threshold, indicating that the quality of the sterile medical instrument in the type is unqualified, and if the comprehensive quality influence coefficient of a certain sterile medical instrument in a certain type is larger than or equal to the set quality influence coefficient threshold, indicating that the quality of the sterile medical instrument in the type is qualified, and counting each qualified sterile medical instrument in each type to be stored in the warehouse.
As a further improvement of the present invention, the medical device expiration date acquiring module is configured to acquire a production date of each qualified sterile medical device of each type to be put into the warehouse, and analyze an expiration date of each qualified sterile medical device of each type to be put into the warehouse.
As a further improvement of the present invention, the sterile medical instrument storage management module is configured to sequentially place each qualified sterile medical instrument of each type to be stored in the warehouse into a corresponding type sterile medical instrument storage area in the warehouse, and arrange each qualified sterile medical instrument in each type sterile medical instrument storage area in the warehouse according to an order from short to long validity periods.
The invention has the beneficial effects that: 1. the invention provides an intelligent commodity product storage management system for a medical instrument production and sale warehouse, which can improve the detection efficiency, increase the detection accuracy, effectively avoid the problem of bacterial infection of the sterile medical instrument, ensure the safety use performance of the sterile medical instrument, detect the surface bacteria falling area and the packaging weight of each type of the sterile medical instrument to be put into the warehouse, analyze the surface bacterial colony area ratio and the dryness of the sterile package of each type of the sterile medical instrument to be put into the warehouse, extract the sterilization time of each type of the sterile medical instrument to be put into the warehouse, analyze the remaining sterilization effect retention time of each type of the sterile medical instrument to be put into the warehouse, and calculating the comprehensive quality influence coefficient which accords with the sterile medical instrument in each type to be put into the warehouse, thereby realizing the quality safety of the sterile medical instrument in multi-aspect factor analysis and improving the accuracy and reliability of the quality analysis of the sterile medical instrument.
2. The invention obtains the production date of each qualified sterile medical instrument in each type to be entered into the warehouse by comparing and screening each qualified sterile medical instrument in each type to be entered into the warehouse, analyzes the effective period duration of each qualified sterile medical instrument in each type to be entered into the warehouse, and arranges and places the medical instruments in the storage areas of the corresponding type of sterile medical instruments in the warehouse according to the sequence from short to long of the effective period durations, thereby effectively avoiding the phenomenon that the sterile medical instruments are invalid, improving the medical use safety of the sterile medical instruments and ensuring the body health of people using the sterile medical instruments.
Drawings
In order to more clearly illustrate the technical solutions of the embodiments of the present invention, the drawings used in the description of the embodiments are briefly introduced below, and it is obvious that the drawings in the description below are only some embodiments of the present invention, and it is obvious for those skilled in the art that other drawings can be obtained according to the drawings without creative efforts.
FIG. 1 is a schematic view of the present invention.
Detailed Description
The technical solutions in the embodiments of the present invention will be clearly and completely described below with reference to the drawings in the embodiments of the present invention, and it is obvious that the described embodiments are only a part of the embodiments of the present invention, and not all of the embodiments. All other embodiments, which can be derived by a person skilled in the art from the embodiments given herein without making any creative effort, shall fall within the protection scope of the present invention.
Referring to fig. 1, the present invention provides an intelligent management system for storing finished goods in a medical equipment production and sales warehouse, which includes a sterile medical equipment classification module, a package tightness conformity screening module, a medical equipment parameter detection module, a medical equipment parameter analysis module, a sterilization effect retention time acquisition module, a sterile medical equipment quality analysis module, a medical equipment validity period acquisition module, a sterile medical equipment storage management module, and a storage database.
The sterile medical instrument classification module is connected with the package sealing performance conformity screening module, the package sealing performance conformity screening module is respectively connected with the medical instrument parameter detection module and the sterilization effect retention time acquisition module, the medical instrument parameter analysis module is respectively connected with the medical instrument parameter detection module, the sterile medical instrument quality analysis module and the storage database, the sterilization effect retention time acquisition module is respectively connected with the sterile medical instrument quality analysis module and the storage database, the sterile medical instrument quality analysis module is respectively connected with the storage database and the medical instrument validity period acquisition module, and the sterile medical instrument storage management module is connected with the medical instrument validity period acquisition module.
The sterile medical apparatus and instrument classifying module is used for acquiring the commodity name corresponding to each sterile medical apparatus and instrument to be entered into the medical apparatus and instrument production and sale warehouse, contrastively analyzing the commodity type corresponding to each sterile medical apparatus and instrument to be entered into the medical apparatus and instrument production and sale warehouse, counting each sterile medical apparatus and instrument to be entered into each type of the medical apparatus and instrument production and sale warehouse, numbering each sterile medical apparatus and instrument to be entered into each type of the medical apparatus and instrument production and sale warehouse, and forming a sterile medical apparatus and instrument number set A in each type of the medical apparatus and instrument production and sale warehouseib＝{Aib1，Aib2，...，Aibj，...，Aibm}，AibjDenoted as the jth sterile medical instrument number of the ith type to be entered into the medical instrument production and sales warehouse, where i ═ 1, 2.
The package tightness conformity screening module is used for screening various sterile medical instruments with the package tightness conformity in various types to be fed into a medical instrument production and sales warehouse, and the screening steps are as follows: s11, by checking the integrity of the seal of each sterile medical device package of each type to be entered into the medical device manufacturing and distribution warehouse.
S12, comparing the seal integrity of each sterile medical device package of each type to be entered into the warehouse to the set package seal integrity.
And S13, if the sealing integrity of the package of the sterile medical instrument in a certain type to be put into the warehouse is more than or equal to the set packaging sealing integrity, indicating that the package sealing integrity of the sterile medical instrument in the certain type is satisfied.
S14, screening statistics to be entered into a warehousePackaging sterile medical instruments with consistent sealing performance in each type, recording the sterile medical instruments with consistent packaging sealing performance as the sterile medical instruments with consistent sealing performance, and marking the serial numbers of the sterile medical instruments with consistent sealing performance in each type to be put into a warehouse as AicrWherein r is 1, 2.
Further, the package tightness conformity screening module further comprises a step of counting each sterile medical instrument with inconsistent package tightness in each type to be put into the warehouse and placing the sterile medical instrument in an unqualified commodity area in the warehouse if the sealing integrity of the package of the sterile medical instrument in the type to be put into the warehouse is smaller than the set package sealing integrity, which indicates that the package tightness of the sterile medical instrument in the type is not accordant.
Specifically, the invention screens each sterile medical instrument with the sealing performance according with each type of the package in the warehouse by detecting the sealing integrity of each sterile medical instrument package in each type of the package in the warehouse, thereby improving the detection efficiency, increasing the detection accuracy, effectively avoiding the problem of bacterial infection of the sterile medical instrument and ensuring the safe use performance of the sterile medical instrument.
The medical instrument parameter detection module is used for detecting relevant parameters which accord with sterile medical instruments in various types to enter the warehouse, and the detection steps are as follows: and S21, respectively carrying out optical scanning on the surface of each sterile medical instrument in each type to be put into the warehouse, and acquiring the surface gray scale image of each sterile medical instrument in each type to be put into the warehouse.
S22, extracting the surface bacterial colony area of each sterile medical instrument in each type to be stored in the warehouse, and marking the surface bacterial colony area of each sterile medical instrument in each type to be stored in the warehouse as Sicr。
S23, detecting the packaging weight of each sterile medical apparatus in each type to be put into the warehouse, and marking the packaging weight of each sterile medical apparatus in each type to be put into the warehouse as gicr。
The medical instrument parameter analysis module is used for analyzing relevant parameters which accord with sterile medical instruments in various types to enter the warehouse, and the specific analysis steps are as follows: and S31, extracting the standard surface area of each type of sterile medical instrument stored in the storage database, and analyzing the surface colony area ratio of each type of sterile medical instrument to be stored in the warehouse.
And S32, extracting the standard package weight and the standard sterile package weight of each type of sterile medical instrument stored in the storage database, and analyzing the dryness of each sterile package meeting the sterile medical instrument in each type to be stored in the warehouse.
Further, the medical device parameter analysis module is used for analyzing the colony area ratio of the surface of each type of the medical device conforming to the sterility in the warehouse, and comprises the following steps: the surface colony area s of each type of sterile medical instruments to be put into the warehouseicrSubstituting into formula
Obtaining the area ratio k of surface bacterial colony conforming to each sterile medical instrument in each type to be put into the warehouseicrIn which S isSign boardAiExpressed as the standard surface area of the i-th type of sterile medical instrument.
Further, the medical device parameter analysis module is used for analyzing the dryness of each sterile pack which accords with the sterile medical device in each type to be put into the warehouse, and comprises the following steps: the weight g of each package conforming to the sterile medical device in each type to be put into the warehouseicrSubstitution formula
Obtaining the dryness theta of each sterile pack which accords with the sterile medical instruments in each type to be put into the warehouseicrWhere μ is expressed as a correction factor for the dryness of the sterile package in the packaging of the medical device, g SignAiExpressed as the standard packaging weight, G ', of the ith type of sterile medical device'Sign boardExpressed as the standard sterile package weight in the medical device package.
Specifically, the surface colony area ratio and the aseptic package dryness of each type of the medical instruments meeting the requirements of the sterile medical instruments are analyzed by detecting the surface colony area and the package weight of each type of the medical instruments meeting the requirements of the sterile medical instruments to be put into the warehouse, and reliable reference data are provided for later analysis of the comprehensive quality influence coefficient of each type of the medical instruments meeting the requirements of the sterile medical instruments.
The sterilization effect retention time acquisition module is used for acquiring the remaining sterilization effect retention time which accords with the sterile medical instrument in each type to be put into the warehouse, and the method specifically comprises the following steps: s41, obtaining the packaging information of each sterile medical instrument in each type to be stored in the warehouse, extracting the sterilization time of each sterile medical instrument in each type to be stored in the warehouse, and marking the sterilization time of each sterile medical instrument in each type to be stored in the warehouse as ticr。
S42, extracting the standard sterilization effect keeping time of each type of sterile medical instrument stored in the storage database, and analyzing the remaining sterilization effect keeping time of each type of sterile medical instrument to be stored in the warehouse.
Further, the sterilization effect retention time acquisition module is configured to analyze remaining sterilization effect retention time conforming to each sterile medical instrument in each type of the medical instrument to be put into the warehouse, and includes: the sterilization time t of each type of medical apparatus meeting the requirement of sterility in each type of warehouseicrSubstituting into formula t'icr＝TSignAi-(tReal-time-ticr) Obtaining the remaining sterilization effect retention time t 'of each type of medical instruments meeting the sterility in the warehouse'icrWherein T isSign boardAiExpressed as the standard sterilization effect retention time, t, for the ith type of sterile medical instrumentReal timeIndicated as the current real time.
Specifically, the sterilization time of each conforming sterile medical instrument in each type to be put into the warehouse is extracted, the remaining sterilization effect retention time of each conforming sterile medical instrument in each type is analyzed, and guiding reference data are provided for analyzing the comprehensive quality influence coefficient of each conforming sterile medical instrument in the later period.
The sterile medical instrument quality analysis module is used for calculating the comprehensive quality influence coefficient of each sterile medical instrument in each type to be stored in the warehouse and comparing and counting each qualified sterile medical instrument in each type to be stored in the warehouse.
Further, the calculation formula of the comprehensive quality influence coefficient of each sterile medical instrument in each type to be put into the warehouse is 
ξicrExpressed as the combined quality impact coefficient, λ, of the ith compliant sterile medical instrument of the ith type to be entered into the warehousek、λθ、λtRespectively expressed as the mass influence weight coefficient, k, of the surface colony area ratio, the dryness of the sterile package, and the remaining sterilization effect retention time of the sterile medical instrumenticrExpressed as the surface colony area ratio, theta, of the ith type to be entered into the warehouse in conformity with the sterile medical instrumenticrIs expressed as the dryness, t 'of the sterile pack of the ith conforming sterile medical instrument of the ith type to be entered into the warehouse'icrExpressed as the remaining sterilization effect retention time of the ith compliant sterile medical instrument of the ith type to be entered into the warehouse.
Further, the sterile medical instrument quality analysis module is used for performing comparative statistics on qualified sterile medical instruments of various types to be put into the warehouse, and comprises the following steps: comparing the comprehensive quality influence coefficient of each sterile medical instrument in each type to be stored in the warehouse with a set quality influence coefficient threshold, if the comprehensive quality influence coefficient of a certain sterile medical instrument in a certain type is smaller than the set quality influence coefficient threshold, indicating that the quality of the sterile medical instrument in the type is unqualified, and if the comprehensive quality influence coefficient of a certain sterile medical instrument in a certain type is larger than or equal to the set quality influence coefficient threshold, indicating that the quality of the sterile medical instrument in the type is qualified, and counting each qualified sterile medical instrument in each type to be stored in the warehouse.
Specifically, the comprehensive quality influence coefficient of each sterile medical instrument in each type to be put into the warehouse is calculated, so that the quality safety of the sterile medical instrument is analyzed by various factors, and the accuracy and the reliability of the quality analysis of the sterile medical instrument are improved.
The medical instrument validity period acquisition module is used for acquiring the production date of each qualified sterile medical instrument in each type to be put into the warehouse and analyzing the validity period of each qualified sterile medical instrument in each type to be put into the warehouse.
The sterile medical instrument storage management module is used for sequentially placing all qualified sterile medical instruments in all types to be stored in the warehouse to the sterile medical instrument storage areas of the corresponding types in the warehouse, and arranging and placing all the qualified sterile medical instruments in all the sterile medical instrument storage areas in the warehouse according to the sequence from short to long in effective period.
Further, the sterile medical instrument storage management module comprises a standard storage area environment for extracting sterile medical instruments of various types, dividing the qualified commodity area in the warehouse into sterile medical instrument storage areas of various types, and adjusting the sterile medical instrument storage area environment of various types to the standard storage area environment of the corresponding sterile medical instrument.
Specifically, the production date of each qualified sterile medical instrument in each type to be entered into the warehouse is obtained by comparing and screening each qualified sterile medical instrument in each type to be entered into the warehouse, the effective period duration of each qualified sterile medical instrument in each type to be entered into the warehouse is analyzed, and the qualified sterile medical instruments are sequentially arranged and placed in the corresponding type sterile medical instrument storage areas in the warehouse according to the sequence from short to long effective period durations, so that the phenomenon that the sterile medical instruments fail is effectively avoided, the medical use safety of the sterile medical instruments is improved, and the body health of people using the sterile medical instruments is guaranteed.
The foregoing is merely exemplary and illustrative of the principles of the present invention and various modifications, additions and substitutions of the specific embodiments described herein may be made by those skilled in the art without departing from the principles of the present invention or exceeding the scope of the claims set forth herein.
Claims (10)
1. The utility model provides a medical instrument production sales warehouse commodity finished product stores intelligent management system which characterized in that: the system comprises a sterile medical instrument classification module, a package tightness conformity screening module, a medical instrument parameter detection module, a medical instrument parameter analysis module, a sterilization effect retention time acquisition module, a sterile medical instrument quality analysis module, a medical instrument validity period acquisition module, a sterile medical instrument storage management module and a storage database;
The package tightness conformity screening module is used for screening various sterile medical instruments with the package tightness conformity in various types to be fed into a medical instrument production and sales warehouse, and the screening steps are as follows:
s11, detecting the sealing integrity of each aseptic medical instrument package in each type in the medical instrument production and sale warehouse;
s12, comparing the sealing integrity of each aseptic medical instrument package in each type to be stored in the warehouse with the set sealing integrity of the package;
s13, if the sealing integrity of the package of a certain sterile medical instrument in a certain type to be put into the warehouse is more than or equal to the set sealing integrity of the package, indicating that the package sealing integrity of the sterile medical instrument in the certain type is in accordance;
s14, screening and counting each aseptic medical apparatus with the packing sealing performance in each type in the warehouse, recording each aseptic medical apparatus with the packing sealing performance as each aseptic medical apparatus with the packing sealing performance, and marking the serial number of each aseptic medical apparatus with the packing sealing performance as AicrWherein r is 1, 2.. times.f;
the medical instrument parameter detection module is used for detecting relevant parameters which accord with sterile medical instruments in various types to enter the warehouse, and the detection steps are as follows:
S21, respectively carrying out optical scanning on the surfaces of the sterile medical instruments in the types to be put into the warehouse to obtain surface gray level images of the sterile medical instruments in the types to be put into the warehouse;
s22, extracting the surface bacterial colony area of each sterile medical instrument in each type to be stored in the warehouse, and marking the surface bacterial colony area of each sterile medical instrument in each type to be stored in the warehouse as Sicr；
S23, detecting the packaging weight of each sterile medical apparatus in each type to be put into the warehouse, and marking the packaging weight of each sterile medical apparatus in each type to be put into the warehouse as gicr；
The medical instrument parameter analysis module is used for analyzing relevant parameters which accord with sterile medical instruments in various types to enter the warehouse, and the specific analysis steps are as follows:
s31, extracting the standard surface area of each type of sterile medical instrument stored in the storage database, and analyzing the surface colony area ratio of each type of sterile medical instrument to be stored in the warehouse;
s32, extracting the standard package weight and the standard sterile package weight of each type of sterile medical instrument stored in the storage database, and analyzing the dryness of each sterile package meeting the sterile medical instrument in each type to be stored in the warehouse;
The sterilization effect retention time acquisition module is used for acquiring the remaining sterilization effect retention time which accords with sterile medical instruments in various types to be put into the warehouse, and the method specifically comprises the following steps:
s41, obtaining the packaging information of each sterile medical instrument in each type to be stored in the warehouse, extracting the sterilization time of each sterile medical instrument in each type to be stored in the warehouse, and marking the sterilization time of each sterile medical instrument in each type to be stored in the warehouse as ticr；
S42, extracting the standard sterilization effect holding time of each type of sterile medical apparatus stored in the storage database, and analyzing the remaining sterilization effect holding time of each type of sterile medical apparatus to be stored in the warehouse, wherein the remaining sterilization effect holding time accords with the sterile medical apparatus;
the sterile medical apparatus quality analysis module is used for calculating comprehensive quality influence coefficients of various types of sterile medical apparatuses to be stored in the warehouse, and comparing and counting the qualified sterile medical apparatuses in the various types of sterile medical apparatuses to be stored in the warehouse.
2. The medical equipment production and sales warehouse commodity finished product storage intelligent management system according to claim 1, characterized in that: the sterile medical apparatus classification module is used for acquiring commodity names corresponding to all sterile medical apparatuses to enter the medical apparatus production and sale warehouse, contrastively analyzing commodity types corresponding to all sterile medical apparatuses to enter the medical apparatus production and sale warehouse, counting all sterile medical apparatuses in all types to enter the medical apparatus production and sale warehouse, numbering all sterile medical apparatuses in all types to enter the medical apparatus production and sale warehouse, and forming a sterile medical apparatus numbering set A in all types to enter the medical apparatus production and sale warehouse ib＝{Aib1，Aib2，...，Aibj，...，Aibm}，AibjDenoted as the jth sterile medical instrument number of the ith type to be entered into the medical instrument production and sales warehouse, where i ═ 1, 2.
3. The medical equipment production and sales warehouse commodity finished product storage intelligent management system according to claim 1, characterized in that: the package tightness conformity screening module further comprises a step of counting each sterile medical instrument with inconsistent package tightness in each type to be put into the warehouse and placing the sterile medical instrument in an unqualified commodity area in the warehouse if the sealing integrity of the package of the sterile medical instrument in the type to be put into the warehouse is less than the set package sealing integrity, which indicates that the package tightness of the sterile medical instrument in the type is not accordant.
4. The medical equipment production and sales warehouse commodity finished product storage intelligent management system according to claim 1, characterized in that: the medical instrument parameter analysis module is used for analyzing the surface colony area ratio of each type of sterile medical instruments to be put into the warehouse, and comprises the following components:
the surface colony area s of each type of sterile medical instruments to be put into the warehouseicrSubstituting into formula
Obtaining the area ratio k of surface bacterial colony conforming to each sterile medical instrument in each type to be put into the warehouse icrIn which S isSignAiExpressed as the standard surface area of the i-th type of sterile medical instrument.
5. The medical equipment production and sale warehouse commodity finished product storage intelligent management system according to claim 1, wherein: the medical instrument parameter analysis module is used for analyzing the dryness of each sterile pack which accords with the sterile medical instrument in each type to be put into the warehouse, and comprises the following components:
the weight g of each package conforming to the sterile medical device in each type to be put into the warehouseicrSubstituting into formula
Obtaining the dryness theta of each sterile pack which accords with the sterile medical instruments in each type to be put into the warehouseicrWhere μ is expressed as a correction factor for the dryness of the sterile package in the packaging of the medical device, gSign boardAiExpressed as the standard packaging weight, G ', of the ith type of sterile medical device'Sign boardExpressed as the weight of a standard sterile pack in the medical device package.
6. The medical equipment production and sale warehouse commodity finished product storage intelligent management system according to claim 1, wherein: the sterilization effect retention time acquisition module is used for analyzing the remaining sterilization effect retention time which accords with the sterile medical instrument in each type to be put into the warehouse, and comprises the following steps:
the sterilization time t of each type of medical instruments meeting the requirement of sterility in each type to be put into the warehouse icrSubstituting into formula t'icr＝TSignAi-(tReal time-ticr) Obtaining the remaining sterilization effect retention time t 'of each type of medical instruments meeting the sterility in the warehouse'icrWherein T isSign boardAiExpressed as the standard sterilization effect retention time, t, for the ith type of sterile medical instrumentReal timeIndicated as the current real time.
7. The medical equipment production and sale warehouse commodity finished product storage intelligent management system according to claim 1, wherein: the calculation formula of the comprehensive quality influence coefficient of each sterile medical instrument in each type to be put into the warehouse is
ξicrExpressed as the combined quality impact coefficient, λ, of the ith compliant sterile medical instrument of the ith type to be entered into the warehousek、λθ、λtRespectively expressed as the mass influence weight coefficient, k, of the surface colony area ratio, the dryness of the sterile package, and the remaining sterilization effect retention time of the sterile medical instrumenticrExpressed as the surface colony area ratio, theta, of the ith type to be entered into the warehouse in conformity with the sterile medical instrumenticrIs expressed as the dryness, t 'of the sterile pack of the ith conforming sterile medical instrument of the ith type to be entered into the warehouse'icrExpressed as the remaining sterilization effect retention time of the ith compliant sterile medical instrument of the ith type to be entered into the warehouse.
8. The medical equipment production and sale warehouse commodity finished product storage intelligent management system according to claim 1, wherein: the quality analysis module of the sterile medical apparatus is used for comparing and counting the qualified sterile medical apparatus in each type to be stored in the warehouse, and comprises the following components:
comparing the comprehensive quality influence coefficient of each sterile medical instrument in each type to be stored in the warehouse with a set quality influence coefficient threshold, if the comprehensive quality influence coefficient of a certain sterile medical instrument in a certain type is smaller than the set quality influence coefficient threshold, indicating that the quality of the sterile medical instrument in the type is unqualified, and if the comprehensive quality influence coefficient of a certain sterile medical instrument in a certain type is larger than or equal to the set quality influence coefficient threshold, indicating that the quality of the sterile medical instrument in the type is qualified, and counting each qualified sterile medical instrument in each type to be stored in the warehouse.
9. The medical equipment production and sale warehouse commodity finished product storage intelligent management system according to claim 1, wherein: the medical instrument validity period acquiring module is used for acquiring the production date of each qualified sterile medical instrument in each type to be put into the warehouse and analyzing the validity period of each qualified sterile medical instrument in each type to be put into the warehouse.
10. The medical equipment production and sales warehouse commodity finished product storage intelligent management system according to claim 1, characterized in that: the sterile medical instrument storage management module is used for sequentially placing all qualified sterile medical instruments in all types to be stored in the warehouse to the sterile medical instrument storage areas of the corresponding types in the warehouse, and arranging and placing all the qualified sterile medical instruments in all the sterile medical instrument storage areas in the warehouse according to the sequence from short to long in effective period.
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