JPH0432967A - Clitical examination total information system - Google Patents
Clitical examination total information systemInfo
- Publication number
- JPH0432967A JPH0432967A JP2067047A JP6704790A JPH0432967A JP H0432967 A JPH0432967 A JP H0432967A JP 2067047 A JP2067047 A JP 2067047A JP 6704790 A JP6704790 A JP 6704790A JP H0432967 A JPH0432967 A JP H0432967A
- Authority
- JP
- Japan
- Prior art keywords
- time
- examined
- examination
- test
- information
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
- 238000012360 testing method Methods 0.000 claims description 40
- 238000000034 method Methods 0.000 claims description 8
- 238000012544 monitoring process Methods 0.000 claims 1
- 238000005259 measurement Methods 0.000 abstract description 8
- 230000003111 delayed effect Effects 0.000 abstract description 4
- 238000004886 process control Methods 0.000 description 5
- 238000010586 diagram Methods 0.000 description 3
- 239000012141 concentrate Substances 0.000 description 2
- 230000001934 delay Effects 0.000 description 2
- 238000005516 engineering process Methods 0.000 description 2
- 238000007689 inspection Methods 0.000 description 2
- 239000008280 blood Substances 0.000 description 1
- 210000004369 blood Anatomy 0.000 description 1
- 238000009534 blood test Methods 0.000 description 1
- 238000003745 diagnosis Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 230000010365 information processing Effects 0.000 description 1
- 238000005070 sampling Methods 0.000 description 1
Landscapes
- Automatic Analysis And Handling Materials Therefor (AREA)
- Measuring And Recording Apparatus For Diagnosis (AREA)
- Medical Treatment And Welfare Office Work (AREA)
Abstract
Description
【発明の詳細な説明】
〔産業上の利用分野〕
本発明は、病院等の臨床検査室における検査情報システ
ムの検査工程管理システム及びその方法に関する。DETAILED DESCRIPTION OF THE INVENTION [Field of Industrial Application] The present invention relates to a test process management system and method for a test information system in a clinical laboratory such as a hospital.
従来のシステムでは、検査結果が情報処理システムに集
められるが、これらの結果は、病院ホストに転送される
のみであり、各検体の検査工程の進捗度のチェックに対
しては何ら手段を持っていなかった。In conventional systems, test results are collected in an information processing system, but these results are only transferred to the hospital host, and there is no way to check the progress of the testing process for each specimen. There wasn't.
このため、至急に検査結果が要求される検体に対する検
査が遅れ、検査依頼元である医師より催促の電話を受け
、検査技師があわてて当該検体の検査を実施しなければ
ならない場合があり、このような例外処理により、最も
検査室にとって重要な検査過誤の発生する遠因ともなっ
ていた。As a result, tests for specimens for which test results are urgently requested may be delayed, and laboratory technicians may have to rush to test the specimens after receiving a reminder call from the doctor requesting the test. Such exception handling has become a contributing factor to the occurrence of test errors, which are most important for laboratories.
また、一般の検査室では、これらの例外処理を防ぐため
、検体受付に多数の技師を配置し、至急検体の区分けを
受付時点で行うなど、本来の検査業務ではない作業に多
くの労力を費やしていた。In addition, in order to prevent these exceptions, in general laboratories, many technicians are assigned to the specimen reception area, and a large amount of labor is spent on tasks that are not part of the original testing work, such as having to urgently sort the specimens at the time of reception. was.
本発明は、従来技術で欠落したいた検査の工程管理を検
査室情報システムにて行うことにより、各検体の工程管
理を確実に実施し、必要な検体のデータを必要な時に確
実に報告できるように、検査技師の業務バックアップを
行うことにある。The present invention uses a laboratory information system to perform process control of tests, which was lacking in conventional technology, so that process control for each sample can be reliably carried out, and necessary sample data can be reliably reported when necessary. The main objective is to provide operational backup for laboratory technicians.
上記目的を達成するために、従来の検査情報システム内
に、各検体のTurn Around Time (検
査室で検体の受は付けを行ってから検査結果を報告する
までの時間)を登録し、個々の検体について受付処理後
の測定結果受入終了までの工程を常にモニタする機能を
付加することにより、検査技師に対し検体測定の工程管
理状態を常に知らせておくシステムとした。In order to achieve the above objectives, the turn around time of each specimen (the time from the time the specimen is received at the laboratory until the report of the test result) is registered in the conventional laboratory information system, and the turn around time of each specimen is registered. By adding a function that constantly monitors the process from sample reception processing to the end of acceptance of measurement results, we created a system that constantly informs laboratory technicians of the process control status of sample measurement.
検査室情報システムでは、各検体のTAT情報を持ち、
検査室での検体受付時を起点とし、この検体に対する情
報の流れを時間と共に遂次チェックする。The laboratory information system has TAT information for each specimen,
Starting from the time the specimen is received in the laboratory, the flow of information regarding the specimen is sequentially checked over time.
これにより規定のTATを超過する恐れのある検体や、
超過した検体に対し、オペレータに対し警報を持って通
報することにより、検査の遅れ等の防止が可能となる。As a result, samples that may exceed the specified TAT,
By notifying the operator of excess samples with an alarm, delays in testing can be prevented.
以下、本発明の一実施例のシステム構成を第1図により
説明する。The system configuration of an embodiment of the present invention will be described below with reference to FIG.
検査室制御システム1には、病院ホストシステム2等か
らの検査依頼情報を受は取る手段と、これらに検査結果
情報を送る手段を持っている。The laboratory control system 1 has means for receiving and receiving test request information from the hospital host system 2 and the like, and means for sending test result information to these.
病院では、医師が患者の診察において、血液検査の必要
性が生じた場合、検査項目を選択し、検査部門に対しこ
の情報を伝達する。At a hospital, when a doctor examines a patient and a blood test becomes necessary, he or she selects the test items and transmits this information to the testing department.
患者の血液は、この情報により採土場で採血され、検査
部門に届けられる。Based on this information, the patient's blood is collected at the sampling site and delivered to the testing department.
検体を受は取った検査部門では、受付処理を行い検体受
付処理端末3の検査項目の確認を行う。The testing department that receives the specimen performs reception processing and checks the testing items on the specimen reception processing terminal 3.
これ以降、検査項目によって、検体は各分析計1゜2.
3iliII御端末6,7,8.9に振り分けられたり
、持ちまわられたりする。From now on, depending on the test item, the sample will be transferred to each analyzer at 1°2.
3iliII terminals 6, 7, 8.9, or carried around.
各分析計で測定された結果は、検査情報ファイル内に記
憶されると共に、病院ホスト等にも転送され、医師の診
断の為の情報として供される。The results measured by each analyzer are stored in the test information file, and are also transferred to a hospital host or the like, where they are provided as information for a doctor's diagnosis.
第2図には、この検査情報ファイル内の一般的な構成を
示す。FIG. 2 shows the general structure within this examination information file.
本発明によれば、第3図に示すように、検体が検査部門
に到着し、受付処理終了後から時間計測を開始し、規定
時間内に、各分析計1.2.3制御端末6,7.8から
検体測定依頼情報の問い合わせがあるまで行い、第4図
に示すように一定時間(T1)を超えれば、検査報告に
遅れが発生する恐れがあるため、第ルベルのアラームを
発生するものとする。According to the present invention, as shown in FIG. 3, time measurement is started after the specimen arrives at the testing department and the reception process is completed, and within the specified time, each analyzer 1, 2, 3 control terminal 6, 7.8 until there is an inquiry about the sample measurement request information, and as shown in Figure 4, if a certain time (T1) is exceeded, there is a risk of a delay in the test report, so the alarm of the second level is generated. shall be taken as a thing.
次に、検体測定依頼情報の問い合わせ後、検査結果が一
定時間(T2)を超えるまでに到着することをチェック
し続け、これを超えた場合は1分析業務における業務遅
延の恐れが有るとして、第2レベルのアラームを発生す
るものとする。Next, after inquiring about the sample measurement request information, we continue to check that the test results arrive within a certain time (T2), and if this is exceeded, there is a risk of delays in the 1 analysis work. A two-level alarm shall be generated.
さらに、到着した結果に何らかのアラームが存在した場
合、オペレータに何らかの処理を要求するが、これにつ
いても一定時間(T8)を超えるまでに処理しなければ
、正確なデータが出力できず、第3レベルのアラームを
発生するものとする。Furthermore, if there is any alarm in the arrived results, the operator is requested to take some action, but if this is not done within a certain period of time (T8), accurate data cannot be output, and the third level shall generate an alarm.
このような、チェックシステムを導入することにより、
従来、検査技師の運用に頼っていたために達成が困難で
あった検査の迅速処理が可能となり、検査技師は、検査
業務に専念することが可能となる。By introducing such a check system,
It is now possible to quickly process tests, which was previously difficult to achieve due to relying on the operation of laboratory technicians, and the laboratory technicians can now concentrate on their inspection work.
本発明によれば、検査技師か本来の業務ではない検体の
選別や医師からの検査結果問い合わせへの対応等の余計
な作業に携わることなく、検査業務に専念することが可
能となる。According to the present invention, it becomes possible for a laboratory technician to concentrate on his or her testing work without having to be involved in unnecessary tasks such as sorting specimens or responding to inquiries about test results from doctors, which are not part of his or her original work.
この結果、検査の迅速化が進められ、各々の検体に要求
されるTAT (ターン・アラウンド・タイム)で検査
業務が遂行されることとなる。As a result, testing will become faster and testing will be performed within the TAT (turn around time) required for each specimen.
分析装置自身も、検査室としては最大処理を考慮した高
価な高処理能力装置を選別する傾向が強い現状から、平
均的処理量を考慮した安価な中形機の選択が可能となり
、ランニングコストの低減。As for the analyzer itself, there is a strong tendency for laboratories to select expensive, high-throughput equipment that takes maximum throughput into consideration, but it is now possible to select inexpensive, medium-sized equipment that takes average throughput into consideration, reducing running costs. reduction.
イニシャルコストの低減を図ることが可能となる。It becomes possible to reduce initial costs.
第1図は本発明の一実施例としてのシステム構成図、第
2図は検査情報システム内の検体情報ファイルの構成図
、第3図は工程管理システムのフローチャート、第4図
はタイミング信号図を示す。
1・・・検査室制御システム、2・・・病院ホストシス
テム、3・・・検体受付処理端末、4・・・検査情報フ
ァイル、5・・・工程管理情報表示端末、6・・・分析
計1制御端末、7・・・分析計2制御端末、8・・・分
析計3制御端末、9・・・用手法検査端末。Fig. 1 is a system configuration diagram as an embodiment of the present invention, Fig. 2 is a configuration diagram of a specimen information file in the test information system, Fig. 3 is a flowchart of the process control system, and Fig. 4 is a timing signal diagram. show. 1... Laboratory control system, 2... Hospital host system, 3... Sample reception processing terminal, 4... Test information file, 5... Process control information display terminal, 6... Analyzer 1 control terminal, 7...analyzer 2 control terminal, 8...analyzer 3 control terminal, 9...method inspection terminal.
Claims (1)
の検査結果入力部と検査依頼情報記憶部と検査結果記憶
部及びこれらの情報をモニタ可能な表示部より成る臨床
検査情報総合システムにおいて、 各検体の依頼情報と検査結果を常にチェックするソフト
ウェアを有することにより、検査工程の進捗度管理を実
施することを特徴とする臨床検査総合情報システム。[Claims] 1. A test request input section, a test sample reception section, a test result input section from each analyzer, a test request information storage section, a test result storage section, and a display section capable of monitoring these information. What is claimed is: 1. A comprehensive clinical test information system comprising software that constantly checks the request information and test results of each specimen to manage the progress of a test process.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2067047A JPH0432967A (en) | 1990-03-19 | 1990-03-19 | Clitical examination total information system |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2067047A JPH0432967A (en) | 1990-03-19 | 1990-03-19 | Clitical examination total information system |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH0432967A true JPH0432967A (en) | 1992-02-04 |
Family
ID=13333541
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2067047A Pending JPH0432967A (en) | 1990-03-19 | 1990-03-19 | Clitical examination total information system |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH0432967A (en) |
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2000046835A (en) * | 1998-07-30 | 2000-02-18 | Hitachi Ltd | System and method for inspecting specimen |
JP2005108209A (en) * | 2003-09-11 | 2005-04-21 | Mitsubishi Kagaku Bio-Clinical Laboratories Inc | Clinical trial examination management system |
JP2008175736A (en) * | 2007-01-19 | 2008-07-31 | Fujitsu Ltd | Abnormality warning system for apparatus, abnormality warning method for apparatus and abnormality warning program for apparatus |
JP2008216263A (en) * | 2008-04-07 | 2008-09-18 | Toshiba Corp | Automatic analyzer |
JP2010249839A (en) * | 2010-06-30 | 2010-11-04 | Toshiba Corp | Automatic analyzer |
WO2012039146A1 (en) * | 2010-09-24 | 2012-03-29 | コニカミノルタエムジー株式会社 | Inspection reservation server and inspection reservation system |
JP2012141149A (en) * | 2010-12-28 | 2012-07-26 | Sysmex Corp | Specimen processing system |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS646554B2 (en) * | 1982-11-11 | 1989-02-03 | Hitachi Ltd |
-
1990
- 1990-03-19 JP JP2067047A patent/JPH0432967A/en active Pending
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS646554B2 (en) * | 1982-11-11 | 1989-02-03 | Hitachi Ltd |
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2000046835A (en) * | 1998-07-30 | 2000-02-18 | Hitachi Ltd | System and method for inspecting specimen |
JP2005108209A (en) * | 2003-09-11 | 2005-04-21 | Mitsubishi Kagaku Bio-Clinical Laboratories Inc | Clinical trial examination management system |
JP2008175736A (en) * | 2007-01-19 | 2008-07-31 | Fujitsu Ltd | Abnormality warning system for apparatus, abnormality warning method for apparatus and abnormality warning program for apparatus |
JP2008216263A (en) * | 2008-04-07 | 2008-09-18 | Toshiba Corp | Automatic analyzer |
JP2010249839A (en) * | 2010-06-30 | 2010-11-04 | Toshiba Corp | Automatic analyzer |
WO2012039146A1 (en) * | 2010-09-24 | 2012-03-29 | コニカミノルタエムジー株式会社 | Inspection reservation server and inspection reservation system |
JP2012141149A (en) * | 2010-12-28 | 2012-07-26 | Sysmex Corp | Specimen processing system |
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