JPS635266A - Analyser - Google Patents
AnalyserInfo
- Publication number
- JPS635266A JPS635266A JP61147153A JP14715386A JPS635266A JP S635266 A JPS635266 A JP S635266A JP 61147153 A JP61147153 A JP 61147153A JP 14715386 A JP14715386 A JP 14715386A JP S635266 A JPS635266 A JP S635266A
- Authority
- JP
- Japan
- Prior art keywords
- items
- test
- examination
- disease
- disease name
- 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
- 201000010099 disease Diseases 0.000 claims abstract description 28
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims abstract description 28
- 238000012360 testing method Methods 0.000 claims description 44
- 238000006243 chemical reaction Methods 0.000 claims description 12
- 238000005259 measurement Methods 0.000 claims description 6
- 238000007689 inspection Methods 0.000 description 15
- 238000010586 diagram Methods 0.000 description 3
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- 238000007796 conventional method Methods 0.000 description 2
- 210000003743 erythrocyte Anatomy 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 102000001554 Hemoglobins Human genes 0.000 description 1
- 108010054147 Hemoglobins Proteins 0.000 description 1
- 102000008133 Iron-Binding Proteins Human genes 0.000 description 1
- 108010035210 Iron-Binding Proteins Proteins 0.000 description 1
- 208000007502 anemia Diseases 0.000 description 1
- 238000012937 correction Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000005534 hematocrit Methods 0.000 description 1
- 150000002505 iron Chemical class 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 210000000265 leukocyte Anatomy 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 210000002966 serum Anatomy 0.000 description 1
Classifications
-
- G—PHYSICS
- G06—COMPUTING; CALCULATING OR COUNTING
- G06F—ELECTRIC DIGITAL DATA PROCESSING
- G06F40/00—Handling natural language data
- G06F40/10—Text processing
- G06F40/166—Editing, e.g. inserting or deleting
- G06F40/177—Editing, e.g. inserting or deleting of tables; using ruled lines
- G06F40/18—Editing, e.g. inserting or deleting of tables; using ruled lines of spreadsheets
Landscapes
- Engineering & Computer Science (AREA)
- Theoretical Computer Science (AREA)
- Health & Medical Sciences (AREA)
- Artificial Intelligence (AREA)
- Audiology, Speech & Language Pathology (AREA)
- Computational Linguistics (AREA)
- General Health & Medical Sciences (AREA)
- Physics & Mathematics (AREA)
- General Engineering & Computer Science (AREA)
- General Physics & Mathematics (AREA)
- Automatic Analysis And Handling Materials Therefor (AREA)
Abstract
Description
【発明の詳細な説明】 [発明の目的] (産業上の利用分野) 本発明は、検体の成分を測定する分析装置に関する。[Detailed description of the invention] [Purpose of the invention] (Industrial application field) The present invention relates to an analyzer for measuring components of a specimen.
(従来の技術)
従来の分析装置は、依頼された検査項目のうち測定可能
な項目のみ受は付けし、その検査結果を出力するように
なっている。(Prior Art) A conventional analyzer accepts only measurable items among the requested test items, and outputs the test results.
(発明が解決しようとする問題点)
ところが従来の分析装置では、病名に応じて医者が過去
のデータより「必ず測定しなければならない項目」を選
択すると共に、分析装置で検査することができない項目
は除外して、これを検査至の受は付けに依頼しなければ
ならなかった。このため、受は付けに長時間を要し、ま
た依頼ミスが生じやすいという問題があった。(Problem to be solved by the invention) However, with conventional analyzers, doctors select "items that must be measured" from past data according to the disease name, and also select items that cannot be tested with the analyzer. This had to be excluded and this had to be requested to the person in charge of the inspection. For this reason, there was a problem in that it took a long time to process the request and mistakes in requests were likely to occur.
本発明の目的は、以上のような問題点を解決し、受は付
けに要する時間を短縮して医者及び検査苗の労力軽減を
図ると共に、依頼ミスをなくすことにある。It is an object of the present invention to solve the above-mentioned problems, to shorten the time required for receiving orders, to reduce the labor of doctors and test plants, and to eliminate mistakes in requests.
[発明の構成]
(問題点を解決するための手段)
上記目的を達成するため本発明は、病名を入力する検査
受付部と、該検査受付部に入力された病名に応じて病名
をその病名に必要な検査項目に変換すると共にその検査
項目を自動検査可能な項目と不能な項目に判別する検査
項目変換部と、該検査項目変換部で判別された自動検査
可能項目を実行する測定部と、前記検査項目変換部で判
別された自動検査不能項目についてのワークシートを発
行するワークシート発行部とを具備した構成とした。[Structure of the Invention] (Means for Solving the Problems) In order to achieve the above object, the present invention includes a test reception section for inputting a disease name, and a test reception section that inputs a disease name according to the disease name input to the test reception section. an inspection item conversion unit that converts the inspection items into inspection items necessary for the test and distinguishes the inspection items into items that can be automatically inspected and items that cannot be automatically inspected; and a measurement unit that executes the automatically inspectable items that are determined by the inspection item conversion unit. , and a worksheet issuing section that issues a worksheet for the items that cannot be automatically inspected as determined by the inspection item converting section.
(作 用) 本発明は上記の構成としたので、次のように作用する。(for production) Since the present invention has the above configuration, it operates as follows.
即ち、検査受付部に病名を入力すると、検査項目変換部
が検査受付部に入力された病名に応じて病名をその病名
に必要な検査項目に変換すると共にその検査項目を自動
検査可能な項目と不能な項目に判別する。そして、該検
査項目変換部で判別された自動検査項目については測定
部で検査が実行され、自動検査不能項目についてはワー
クシートが2−クシート発行部によって発行され、この
シート基づき検査者が検査を実行することとなる。That is, when a disease name is input into the test reception section, the test item conversion section converts the disease name into the test items necessary for that disease name according to the disease name input into the test reception section, and converts the test items into items that can be automatically tested. It is determined that the item is impossible. Then, the automatic inspection items determined by the inspection item conversion unit are inspected by the measurement unit, and for items that cannot be automatically inspected, a worksheet is issued by the 2-sheet issuing unit, and the inspector performs the inspection based on this sheet. It will be executed.
従って本発明によれば、検査受付部に病名を入力するだ
けで必要検査項目が測定部及び検査者により検査される
ので、従来に比べて受は付けに要する時間が短縮され、
医者及び倹査至の労力が著しく軽減される。又、病名を
入力するだけなので依頼ミスもなくなる。Therefore, according to the present invention, only by inputting the disease name into the test reception section, the necessary test items are examined by the measurement section and the examiner, so the time required for reception is shortened compared to the conventional method.
The effort of doctors and medical examiners is significantly reduced. Also, since you only have to enter the disease name, there will be no mistakes in making requests.
(実施例) 以下図示の実施例について説明する。(Example) The illustrated embodiment will be described below.
第1図は本発明に係る分析装置のブロック図である。FIG. 1 is a block diagram of an analyzer according to the present invention.
1は検査受付部であり、病名をキーとしてキー人力する
ことができるようになっている。Reference numeral 1 is the test reception department, which allows users to enter information using the disease name as a key.
2は検査項目変換部であって、第2図に示すような変換
テーブルを備えており、検査受付部1で入力された病名
に応じて、これをその病名に必要な検査項目に変換する
ようになっている。例えば病名として「貧血」を入力し
た場合には、1赤面球数 2ヘモグロビン濃
度3ヘマトクリット値 4網状赤面球数5白血球数
6血小板数
7血清鉄値 8不飽和鉄結合能9クームス試
験
等の検査項目が取り出されるようになっている。Reference numeral 2 denotes a test item conversion unit, which is equipped with a conversion table as shown in FIG. It has become. For example, if you enter "anemia" as the disease name, 1. Number of red blood cells, 2. Hemoglobin concentration, 3. Hematocrit value, 4. Number of reticulated red blood cells, 5. Number of white blood cells.
Test items such as 6 platelet count 7 serum iron level 8 unsaturated iron binding capacity 9 Coombs test are now available.
第2図に於て、Fは必要な検査項目を示すフラッグであ
る。又、この検査項目変換部2は、上記検査項目のうち
、この分析装置が備えている測定部3で自動的に検査可
能な検査項目と検査不能な検査項目とを判別するように
なっている。この判別は第3図に示すようなテーブル内
の情報に基づき行なわれる。第3図では、検査項目とこ
れに対応する分析装置情報とが示され、同図において前
記情報が「1」である項目はこの分析装置が備える測定
部3で検査され、前記情報がrOJである項目は用手法
によって検査されることを示している。In FIG. 2, F is a flag indicating necessary inspection items. Further, the test item converter 2 is configured to distinguish between test items that can be automatically tested and test items that cannot be automatically tested by the measuring unit 3 included in the analyzer, among the above test items. . This determination is made based on information in a table as shown in FIG. In FIG. 3, inspection items and corresponding analyzer information are shown, and in the same figure, items for which the information is "1" are inspected by the measuring section 3 included in this analyzer, and the said information is rOJ. Indicates that certain items will be inspected manually.
そして、検査可能な項目については測定部3に、検査不
能な項目についてはワークシート発行部5にそれぞれそ
のデータを出力するようになっている。測定部3は、検
査項目変換部2からの検査項目を入力すると、その項目
の検査を実行するようになっている。−方、ワークシー
ト発行部5は検査項目変換部2からのデータを入力する
と第4図に示すようなワークシートSを発行するように
なっている。The data for items that can be inspected are output to the measuring section 3, and the data for items that cannot be inspected are output to the worksheet issuing section 5. When the measurement section 3 receives an inspection item from the inspection item conversion section 2, it executes an inspection of that item. - On the other hand, when the worksheet issuing section 5 receives data from the test item converting section 2, it issues a worksheet S as shown in FIG.
6はデータ入力部であり、以上のようなワークシートS
に基づき検査者が他の分析装置又は用手法により検査し
た検査結果を入力するようになっている。6 is the data input section, and the worksheet S as shown above is
Based on this, the inspector inputs the test results obtained using other analytical devices or manual methods.
4はメモリであり、前記測定部3による検査結果及びデ
ータ入力部6からの検査結果を記憶するようになってい
る。Reference numeral 4 denotes a memory, which stores the test results from the measuring section 3 and the test results from the data input section 6.
7はデータ修正部であり、メモリ4に記憶されているデ
ータを読み出して、これを修正するようになっている。Reference numeral 7 denotes a data modification section, which reads data stored in the memory 4 and modifies it.
例えば温度、湿度、圧力の状態によってベースラインが
変わってくるので、ベースラインの補正をかけるように
なっている。For example, the baseline changes depending on the temperature, humidity, and pressure conditions, so the baseline is corrected.
8は表示部であり、データ修正部7で修正された検査結
果を表示するようになっている。又、この表示部は8は
報告古発行部を備えており、病名に応じてその病名の検
査データとして必要なデータのみを印刷した病名毎の報
告書を発行するようになっている。Reference numeral 8 denotes a display section, which displays the test results corrected by the data correction section 7. Further, this display section 8 is equipped with an old report issuing section, and is adapted to issue a report for each disease name in which only data necessary as test data for that disease name is printed according to the disease name.
以上のような装置によれば、検査受付部1に病名を入力
するだけで必要検査項目が測定部3および他装置等によ
り検査され、その検査結果が表示部8にて得られる。従
って従来に比べて、受は付けに要する時間が短縮され、
医者及び検査子の労力が著しく軽減される。又、病名を
入力するだけなので依頼ミスもなくなる。According to the above-described apparatus, by simply inputting a disease name into the test receiving section 1, the necessary test items are tested by the measuring section 3 and other devices, and the test results are obtained on the display section 8. Therefore, compared to conventional methods, the time required to attach the receiver is reduced,
The labor of the doctor and the tester is significantly reduced. Also, since you only have to enter the disease name, there will be no mistakes in making requests.
上記本発明の一実施例について説明したが、本発明は上
記実施例に限定されるものではなく、本発明の要旨の範
囲内において適宜変形実施可能であることは言うまでも
ない。Although one embodiment of the present invention has been described above, it goes without saying that the present invention is not limited to the above embodiment and can be modified as appropriate within the scope of the gist of the present invention.
[発明の効果]
以上詳述したように本発明によれば、受は付けに要する
時間が短縮され、医者及び検査子の労力が著しく軽減さ
れる。又、病名を入力するだけなので依頼ミスもなくな
る。[Effects of the Invention] As described in detail above, according to the present invention, the time required for the reception is shortened, and the labor of the doctor and the examiner is significantly reduced. Also, since you only have to enter the disease name, there will be no mistakes in making requests.
第1図は本発明に係る分析装置のブロック図、第2図は
変換テーブルの一例を示す図、第3図は検査項目−分析
装置情報のテーブル例を示す図、第4図はワークシート
発行部から発行されるワークシートの例を示す図である
。
1・・・検査受付部、2・・・検査項目変換部、3・・
・測定部、5・・・ワークシート発行部。
代理人 弁理士 則 近 憲 缶周
大 胡 典 夫第3図Figure 1 is a block diagram of the analyzer according to the present invention, Figure 2 is an example of a conversion table, Figure 3 is an example of a table of test item-analyzer information, and Figure 4 is a worksheet issue. FIG. 3 is a diagram showing an example of a worksheet issued by the department. 1... Test reception department, 2... Test item conversion section, 3...
・Measurement department, 5... Worksheet publishing department. Agent Patent Attorney Nori Chika Ken Shu
Norio Ogo Figure 3
Claims (1)
た病名に応じて病名をその病名に必要な検査項目に変換
すると共にその検査項目を自動検査可能な項目と不能な
項目に判別する検査項目変換部と、該検査項目変換部で
判別された自動検査項目を実行する測定部と、前記検査
項目変換部で判別された自動検査不能項目についてのワ
ークシートを発行するワークシート発行部とを具備した
ことを特徴とする分析装置。A test reception section for inputting a disease name; and a test reception section that converts the disease name into test items necessary for the disease name according to the disease name input into the test reception section, and distinguishes the test items into those that can be automatically tested and those that cannot be automatically tested. a test item conversion unit; a measurement unit that executes the automatic test items determined by the test item conversion unit; and a worksheet issuing unit that issues a worksheet for the automatic test impossible items determined by the test item conversion unit. An analytical device characterized by comprising:
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP61147153A JPS635266A (en) | 1986-06-25 | 1986-06-25 | Analyser |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP61147153A JPS635266A (en) | 1986-06-25 | 1986-06-25 | Analyser |
Publications (1)
Publication Number | Publication Date |
---|---|
JPS635266A true JPS635266A (en) | 1988-01-11 |
Family
ID=15423784
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP61147153A Pending JPS635266A (en) | 1986-06-25 | 1986-06-25 | Analyser |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS635266A (en) |
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5942124A (en) * | 1994-10-20 | 1999-08-24 | Labsystems, Oy | Magnetic particle transfer device |
US6020211A (en) * | 1994-10-20 | 2000-02-01 | Labsystems Oy | Separation of magnetic microparticles involving a preconcentration step |
US6040192A (en) * | 1993-02-01 | 2000-03-21 | Labsystems Oy | Method and means for magnetic particle specific binding assay |
US6065605A (en) * | 1994-10-20 | 2000-05-23 | Labsystems Oy | Two-stage separation method |
US6197597B1 (en) * | 1993-02-01 | 2001-03-06 | Labsystems Oy | Solid phase immunoassay with carriers matching the shape of sample wells |
US6207463B1 (en) | 1994-10-20 | 2001-03-27 | Labsystems Oy | Separation device for microparticles involving a magnetic rod |
-
1986
- 1986-06-25 JP JP61147153A patent/JPS635266A/en active Pending
Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6040192A (en) * | 1993-02-01 | 2000-03-21 | Labsystems Oy | Method and means for magnetic particle specific binding assay |
US6197597B1 (en) * | 1993-02-01 | 2001-03-06 | Labsystems Oy | Solid phase immunoassay with carriers matching the shape of sample wells |
US6447729B1 (en) | 1993-02-01 | 2002-09-10 | Labsystems Oy | Method and means for magnetic particle specific binding assay |
US5942124A (en) * | 1994-10-20 | 1999-08-24 | Labsystems, Oy | Magnetic particle transfer device |
US6020211A (en) * | 1994-10-20 | 2000-02-01 | Labsystems Oy | Separation of magnetic microparticles involving a preconcentration step |
US6065605A (en) * | 1994-10-20 | 2000-05-23 | Labsystems Oy | Two-stage separation method |
US6207463B1 (en) | 1994-10-20 | 2001-03-27 | Labsystems Oy | Separation device for microparticles involving a magnetic rod |
US6448092B1 (en) | 1994-10-20 | 2002-09-10 | Thermo Labsystems Oy | Separation device for microparticles involving a magnetic rod |
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