CN103646305A - Newborn inherited metabolic disease screening information system - Google Patents
Newborn inherited metabolic disease screening information system Download PDFInfo
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- CN103646305A CN103646305A CN201310607525.7A CN201310607525A CN103646305A CN 103646305 A CN103646305 A CN 103646305A CN 201310607525 A CN201310607525 A CN 201310607525A CN 103646305 A CN103646305 A CN 103646305A
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Abstract
The invention discloses a newborn inherited metabolic disease screening information system, which comprises a blood sheet information collection module, a blood sheet checking module, a blood sheet automatic returning and resampling module, a bar code numbering module, an experiment arrangement module, a quality control and result input module, a result auditing and publishing module, a result judging module, a result querying module, a report printing module, a short message notification module, a parent automatic querying module, an automatic positive recalling module, a confidence calculation module, an affair notification module, a fee settlement module and a system setting module. The newborn inherited metabolic disease screening information system is provided with a plurality of information management and querying modules, ensures the uniqueness of serial numbers by using bar code technologies, realizes automatic processing and free management for detection data and screening results, meets requirements of various working modes and is applicable to provincial or municipal screening centers, and realizes the most perfect management quality by using the most convenient management means.
Description
Technical field
The invention belongs to field of information management, relate in particular to a kind of neonate's Inherited Metabolic Disorders examination infosystem.
Background technology
Along with the development of modern medicine, the raising of Clinics, infant mortality rate reduces gradually, and what in the cause of death, account for maximum ratio is exactly birth defect.Each hundred neonate approximately has 4-6 to have birth defect, these defects to have some by inherent cause, to be caused clinically, comprises term single gene extremely and chromosome abnormality, and other are that to be subject to the multiple-factor of heredity and environment abnormal.
Have the congenital metabolic disease of part, in disease, often symptom is not obvious in early days, once morbidity is not threat to life, causes exactly the permanent damage of intelligence or body, brings to family and society and regrets a lifetime and burden.For making inborn defect obtain treating timely and effectively controlling.Medical circle does not have Symptomatic time in early days in disease, just infant can be checked out, and carry out serial of methods, after neonate's birth, soon, just checks, Here it is existing Screening Disease in Neonates.
But the program that existing Screening Disease in Neonates does not have unified rule and can process flexibly, can not, from the multi-faceted demand that meets new sieve professional technique staff, operate more loaded down with trivial details.
Summary of the invention
The object of the present invention is to provide a kind of neonate's Inherited Metabolic Disorders examination infosystem, being intended to can be from the multi-faceted demand that meets new sieve professional technique staff, by newly sieving loaded down with trivial details in each link, random flow process, by software control, become program uniform rules, that can process flexibly, with the easiest ladder of management, realize the most perfect management quality.
The present invention is achieved in that a kind of neonate's Inherited Metabolic Disorders examination infosystem comprises that blood sheet information acquisition module, blood sheet core receive module, blood sheet and automatically return and heavily adopt module, barcode number module, experiment layout module, quality control and result and import module, result audit and release module, result judge module, result queries module, reporting printing module, short breath notification module, the automatic enquiry module of the head of a family, the automatic positive and recall module, confidence statistical module, transaction notification module, disbursement and sattlement module, system module is set.
Described blood sheet information acquisition module can be by blood sampling unit typing, upload, and also can complete typing by examination center, by C/S, is uploaded, is downloaded.
Described blood sheet core receipts module will be received blood sheet and upload blood sheet information and check, blood tablet quality is carried out an acceptance inspection, and check and deliver to painstaking effort sheet quantity and quality in examination with blood sampling unit.
Described blood sheet is automatically return and is heavily adopted module and can automatically return defective blood sheet, and blood sampling unit can receive immediately returns notice, heavily adopts after sample available original data and generates new blood sheet information and upload.
Described barcode number module uses barcode technology to edit blood sheet card number and experiment number, realizes uniqueness and the reliability of blood sampling card number and experiment number, guarantees collection of specimens, sends the accuracy with the identification of experimentation identity.
Described experiment layout module editor tests list, can identify especially special sample, standard items and quality-control product, convenient prompting.Print experiment single, according to singly testing.
Described quality control and result import module experimental result are carried out to Quality Control, and the qualified experimental result of Quality Control can import network by optimum mode.
The audit of described result and release module are carried out secondary and are checked importing result, after auditor signs, after can issue.
Resolution is positive or negative automatically to the numerical value of result for described result judge module, and positive findings has the sign of color and font.
Described result queries module can be received the conditions such as date, audit date by mother's name, blood sampling card number, date of birth, core and carry out Query Result, and the result inquiring in batches derived table lattice file is preserved.
Described reporting printing module can print result report, positive recall notice, return advice note etc.
Described SMS notification module can, by messages in batch after result audit, be notified all person under inspection's screening results and corresponding item.
Described head of a family's self-service query module, the person under inspection head of a family can pass through query site screening results, related announcement and suggestion.
The described automatic positive is recalled the result meeting automatic decision that module is recalled the needs positive, and generates positive recall notice, after blood sampling unit has notice, recalls patient's second mining sample, utilizes the original data of patient to generate new blood sheet information, again uploads.
Described Information Statistics module, by area, by hospital, the condition such as section by date, realizes monthly (or season) form, automatically collects and adds up various data, and system generates various indexs automatically, feeds back various information.
Described transaction notification module facilitates examination center to issue various transaction notification, urge notice and make a definite diagnosis notice, realizes point symmetry groups or point-to-point informing function.
Described disbursement and sattlement module is according to the date terms of user's input, and computational costs, generates cost notifying automatically.
Described system arranges module, and customer administrator can arrange the parameters of system, and critical function is to require to increase, reduce new sieve project according to this area, and experiment parameter is set.Realize the management of system highest weight limit.
effect gathers
Neonate's Inherited Metabolic Disorders examination infosystem of the present invention is provided with a plurality of information management enquiry modules, utilize barcode technology to guarantee the uniqueness of numbering, realization realizes processing automatically and freely manages detecting data and screening results, meet various working methods, provincial or city-level examination center is all suitable for, with the easiest ladder of management, realize the most perfect management quality.
Accompanying drawing explanation
Fig. 1 is the structured flowchart of neonate's Inherited Metabolic Disorders examination infosystem of providing of the embodiment of the present invention.
Embodiment
In order to make object of the present invention, technical scheme and advantage clearer, below in conjunction with drawings and Examples, the present invention is further elaborated.Should be appreciated that specific embodiment described herein, only in order to explain the present invention, is not intended to limit the present invention.
Fig. 1 shows the structured flowchart of neonate's Inherited Metabolic Disorders examination infosystem of the present invention, and as shown in the figure, the present invention is achieved in that a kind of neonate's Inherited Metabolic Disorders examination infosystem comprises
S101: blood sheet information acquisition module;
S102: blood sheet core is received module;
S103: blood sheet is automatically return and heavily adopted module;
S104 barcode number module;
S105: experiment layout module;
S106: quality control and result import module;
S107: result audit and release module;
S108: result judge module;
S109: result queries module;
S110: reporting printing module;
S111: short breath notification module;
S112: the automatic enquiry module of the head of a family;
S113: the positive is recalled module automatically;
S114: confidence statistical module;
S115: transaction notification module;
S116: disbursement and sattlement module;
S117: system arranges module.
Described blood sheet information acquisition module S101 can be by blood sampling unit typing, upload, and also can complete typing by examination center, by C/S, is uploaded, is downloaded.
Described blood sheet core receipts module S102 will receive blood sheet and upload blood sheet information and check, blood tablet quality is carried out an acceptance inspection, and check and deliver to painstaking effort sheet quantity and quality in examination with blood sampling unit.
Described blood sheet is automatically return and is heavily adopted module S103 and can automatically return defective blood sheet, and blood sampling unit can receive immediately returns notice, heavily adopts after sample available original data and generates new blood sheet information and upload.
Described barcode number module S104 uses barcode technology to edit blood sheet card number and experiment number, realizes uniqueness and the reliability of blood sampling card number and experiment number, guarantees collection of specimens, sends the accuracy with the identification of experimentation identity.
It is single that described experiment layout module S105 edits experiment, can identify especially special sample, standard items and quality-control product, convenient prompting.Print experiment single, according to singly testing.
Described quality control and result import module S106 experimental result are carried out to Quality Control, and the qualified experimental result of Quality Control can import network by optimum mode.
The audit of described result and release module S107 carry out secondary and check importing result, after auditor signs, after can issue.
Resolution is positive or negative automatically to the numerical value of result for described result judge module S108, and positive findings has the sign of color and font.
Described result queries module S109 can receive the conditions such as date, audit date by mother's name, blood sampling card number, date of birth, core and carry out Query Result, and the result inquiring in batches derived table lattice file is preserved.
Described reporting printing module S110 can print result report, positive recall notice, return advice note etc.
Described SMS notification module S11 can, by messages in batch after result audit, notify all person under inspection's screening results and corresponding item.
Described head of a family's self-service query module S112, the person under inspection head of a family can pass through query site screening results, related announcement and suggestion.
The described automatic positive is recalled the result meeting automatic decision that module S113 recalls the needs positive, and generates positive recall notice, after blood sampling unit has notice, recalls patient's second mining sample, utilizes the original data of patient to generate new blood sheet information, again uploads.
Described Information Statistics module S114, by area, by hospital, the condition such as section by date, realizes monthly (or season) form, automatically collects and adds up various data, and system generates various indexs automatically, feeds back various information.
Described transaction notification module S115 facilitates examination center to issue various transaction notification, urge notice and make a definite diagnosis notice, realizes point symmetry groups or point-to-point informing function.
Described disbursement and sattlement module S116 is according to the date terms of user's input, and computational costs, generates cost notifying automatically.
Described system arranges module S117, and customer administrator can arrange the parameters of system, and critical function is to require to increase, reduce new sieve project according to this area, and experiment parameter is set.Realize the management of system highest weight limit.
Neonate's Inherited Metabolic Disorders examination infosystem of the present invention is provided with a plurality of information management enquiry modules, utilize barcode technology to guarantee the uniqueness of numbering, realization realizes processing automatically and freely manages detecting data and screening results, meet various working methods, provincial or city-level examination center is all suitable for, with the easiest ladder of management, realize the most perfect management quality.
Although above-mentioned, by reference to the accompanying drawings the specific embodiment of the present invention is described; but be not limiting the scope of the invention; one of ordinary skill in the art should be understood that; on the basis of technical scheme of the present invention, those skilled in the art do not need to pay various modifications that performing creative labour can make or distortion still within protection scope of the present invention.
Claims (6)
1. neonate's Inherited Metabolic Disorders examination infosystem, it is characterized in that, described neonate's Inherited Metabolic Disorders examination infosystem comprises blood sheet information acquisition module, blood sheet core is received module, blood sheet is automatically return and is heavily adopted module, barcode number module, experiment layout module, quality control and result import module, result audit and release module, result judge module, result queries module, reporting printing module, short breath notification module, the automatic enquiry module of the head of a family, automatically the positive is recalled module, confidence statistical module, transaction notification module, disbursement and sattlement module, system arranges module,
Described blood sheet information acquisition module can be by blood sampling unit typing, upload, and also can complete typing by examination center, by C/S, is uploaded, is downloaded;
Described blood sheet core receipts module will be received blood sheet and upload blood sheet information and check, blood tablet quality is carried out an acceptance inspection, and check and deliver to painstaking effort sheet quantity and quality in examination with blood sampling unit;
Described blood sheet is automatically return and is heavily adopted module and can automatically return defective blood sheet, and blood sampling unit can receive immediately returns notice, heavily adopts after sample available original data and generates new blood sheet information and upload;
Described barcode number module uses barcode technology to edit blood sheet card number and experiment number, realizes uniqueness and the reliability of blood sampling card number and experiment number, guarantees collection of specimens, sends the accuracy with the identification of experimentation identity;
Described experiment layout module editor tests list, can identify especially special sample, standard items and quality-control product, convenient prompting.Print experiment single, according to singly testing;
Described quality control and result import module experimental result are carried out to Quality Control, and the qualified experimental result of Quality Control can import network by optimum mode;
The audit of described result and release module are carried out secondary and are checked importing result, after auditor signs, after can issue;
Resolution is positive or negative automatically to the numerical value of result for described result judge module, and positive findings has the sign of color and font;
Described result queries module can be received the conditions such as date, audit date by mother's name, blood sampling card number, date of birth, core and carry out Query Result, and the result inquiring in batches derived table lattice file is preserved;
Described reporting printing module can print result report, positive recall notice, return advice note;
Described SMS notification module can, by messages in batch after result audit, be notified all person under inspection's screening results and corresponding item;
Described head of a family's self-service query module, the person under inspection head of a family can pass through query site screening results, related announcement and suggestion.
2. neonate's Inherited Metabolic Disorders examination infosystem as claimed in claim 1, it is characterized in that, the described automatic positive is recalled the result meeting automatic decision that module is recalled the needs positive, and generate positive recall notice, after having notice, blood sampling unit recalls patient's second mining sample, utilize the original data of patient to generate new blood sheet information, again upload.
3. neonate's Inherited Metabolic Disorders examination infosystem as claimed in claim 1, is characterized in that, described Information Statistics module is by area, by hospital, the condition such as section by date, realize monthly form, automatically collect the various data of statistics, system generates various indexs automatically, feeds back various information.
4. neonate's Inherited Metabolic Disorders examination infosystem as claimed in claim 1, is characterized in that, described transaction notification module facilitates examination center to issue various transaction notification, urge notice and make a definite diagnosis notice, realizes point symmetry groups or point-to-point informing function.
5. neonate's Inherited Metabolic Disorders examination infosystem as claimed in claim 1, is characterized in that, described disbursement and sattlement module is according to the date terms of user's input, and computational costs, generates cost notifying automatically.
6. neonate's Inherited Metabolic Disorders examination infosystem as claimed in claim 1, it is characterized in that, described system arranges module, and customer administrator can arrange the parameters of system, critical function is to require to increase, reduce new sieve project according to this area, and experiment parameter is set.Realize the management of system highest weight limit.
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Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
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CN104134180A (en) * | 2014-07-04 | 2014-11-05 | 中国石油化工股份有限公司 | Screening system and screening method used for multi-factor occupational health examination |
CN104331774A (en) * | 2014-11-14 | 2015-02-04 | 南宁市第二人民医院 | Joint screening and intervention managing system for newborn hearing and deafness susceptibility gene |
CN106295227A (en) * | 2016-08-30 | 2017-01-04 | 王伟佳 | A kind of Prenatal Screening reports management system and management method thereof |
CN107038673A (en) * | 2017-03-28 | 2017-08-11 | 广州市康软信息科技有限公司 | A kind of medical control method and system based on region bar code |
CN107491653A (en) * | 2017-08-30 | 2017-12-19 | 河南爱尔康科技有限公司 | A kind of examination of newborn infant diseases and the management mode of prenatal disease examination |
CN108062977A (en) * | 2017-12-18 | 2018-05-22 | 广东祥岳生物技术有限公司 | A kind of newborn's Screening for Thalassemia result automatic decision system |
CN116189907A (en) * | 2022-12-05 | 2023-05-30 | 广州盛安医学检验有限公司 | Intelligent genetic metabolic disease screening system suitable for newborns |
-
2013
- 2013-11-27 CN CN201310607525.7A patent/CN103646305A/en active Pending
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KAI-PING HSU ET AL.: "A Newborn Screening System Based on Service-Oriented Architecture Embedded Support Vector Machine", 《JOURNAL OF MEDICAL SYSTEMS》 * |
李颖利: "中山市新生儿疾病筛查管理系统的设计与实现", 《中国优秀硕士论文全文数据库 信息科技辑(月刊)》 * |
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Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN104134180A (en) * | 2014-07-04 | 2014-11-05 | 中国石油化工股份有限公司 | Screening system and screening method used for multi-factor occupational health examination |
CN104331774A (en) * | 2014-11-14 | 2015-02-04 | 南宁市第二人民医院 | Joint screening and intervention managing system for newborn hearing and deafness susceptibility gene |
CN106295227A (en) * | 2016-08-30 | 2017-01-04 | 王伟佳 | A kind of Prenatal Screening reports management system and management method thereof |
CN107038673A (en) * | 2017-03-28 | 2017-08-11 | 广州市康软信息科技有限公司 | A kind of medical control method and system based on region bar code |
CN107491653A (en) * | 2017-08-30 | 2017-12-19 | 河南爱尔康科技有限公司 | A kind of examination of newborn infant diseases and the management mode of prenatal disease examination |
CN108062977A (en) * | 2017-12-18 | 2018-05-22 | 广东祥岳生物技术有限公司 | A kind of newborn's Screening for Thalassemia result automatic decision system |
CN116189907A (en) * | 2022-12-05 | 2023-05-30 | 广州盛安医学检验有限公司 | Intelligent genetic metabolic disease screening system suitable for newborns |
CN116189907B (en) * | 2022-12-05 | 2023-09-05 | 广州盛安医学检验有限公司 | Intelligent genetic metabolic disease screening system suitable for newborns |
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Application publication date: 20140319 |