JPH0572175A - Display/record method for result of electrophoresis analysis - Google Patents

Display/record method for result of electrophoresis analysis

Info

Publication number
JPH0572175A
JPH0572175A JP3238080A JP23808091A JPH0572175A JP H0572175 A JPH0572175 A JP H0572175A JP 3238080 A JP3238080 A JP 3238080A JP 23808091 A JP23808091 A JP 23808091A JP H0572175 A JPH0572175 A JP H0572175A
Authority
JP
Japan
Prior art keywords
data
recorded
coordinates
displayed
measured value
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
Application number
JP3238080A
Other languages
Japanese (ja)
Inventor
Hideo Suzuki
秀夫 鈴木
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Olympus Corp
Original Assignee
Olympus Optical Co Ltd
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Olympus Optical Co Ltd filed Critical Olympus Optical Co Ltd
Priority to JP3238080A priority Critical patent/JPH0572175A/en
Publication of JPH0572175A publication Critical patent/JPH0572175A/en
Pending legal-status Critical Current

Links

Abstract

PURPOSE:To quickly perform clinical judgement by inputting data to a measuring means, performing a prescribed calculation so as to display and record first measured values, selecting them according to a clinic purpose and displaying are recording input measured value from combined calculation. CONSTITUTION:Cellulose acetate paper at a carrier in use is cut off by a decided length, it is soaked in buffer solution, blood serum is soaked, and parting images are formed by electrification in an electrophoresis box. The carrier is colored, decolored, and dried so as to perform quantitative measurement by digitmetry, and it is recorded on a recorder. The data is set with coordinates at every output item previously decided, and displayed and recorded as a first measured value. Next, based on the measured value, according to a clinical purpose, for example output items such as name of a patient 1, number of patient 2, data 3, sample number 4, A/G ratio 5, and the coordinates are respectively input, and displayed and recorded as second measured values, and hence a report is prepared. Then, necessary data for clinical judgement can be quickly obtained.

Description

【発明の詳細な説明】Detailed Description of the Invention

【0001】[0001]

【産業上の利用分野】本発明は、自動電気泳動装置によ
り臨床検査分野における血清蛋白質等の蛋白分画測定を
行い、測定値を得る電気泳動分析結果の表示・記録方法
に関するものである。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a method for displaying and recording an electrophoretic analysis result for measuring a protein fraction of a serum protein or the like in a clinical examination field by an automatic electrophoresis apparatus to obtain a measured value.

【0002】[0002]

【従来の技術】血清蛋白質等の検査には、電気泳動法が
用いられている。これは、セルロ−ズアセテ−ト紙等で
形成される支持体の表面に血清を線状に塗布し、これに
通電して血清の分画像を形成させる。この血清分画像を
形成した支持体を染色液により染色し、さらに脱色液に
より脱色し、乾燥させた後、透明化液に漬けて透明化し
た上で比色計で定量を行うというものである。こうして
定量を行った後、測定値を表示・記録するのであるが、
具体的にはデンシトグラム(アナログ波形)と数値によ
って行われる。
2. Description of the Related Art Electrophoresis is used to test serum proteins and the like. In this method, serum is linearly coated on the surface of a support made of cellulose acetate paper or the like, and electricity is applied to the surface to form a serum partial image. The support on which the serum image is formed is stained with a staining solution, further decolorized with a decolorizing solution, dried, and then immersed in a clearing solution to be transparent, and then quantified with a colorimeter. . After quantifying in this way, the measured value is displayed and recorded.
Specifically, it is performed using a densitogram (analog waveform) and a numerical value.

【0003】[0003]

【発明が解決しようとする課題】ところで血清蛋白の検
査を行った場合、アルブミン、α1 グロブリン、β2
ロブリン、γグロブリンの各分画%と、アルブミンとグ
ロブリンの比(A/G 比)といった数値が表示・記録され
る。また、総蛋白量を入力すると、計算により各蛋白濃
度値が表示・記録される。しかしながら、従来の分析結
果の表示・記録方法ではこうした数値とデンシトグラム
しか得られなかった。臨床的な判断の資料としては、こ
の他に「α1 グロブリン+α2 グロブリン」の蛋白濃度
値や「α2 グロブリン/α1 グロブリン」の比等をも必
要とする。これらのデ−タはすでに得られている数値に
基づいて計算をすることにより得られるわけであるが、
検査において臨床的な判断を迅速に行うには、計算に要
する時間がかかり迅速性に欠けるという不具合、さらに
所定項目の数値とこれらの数値を組み合わせ計算した数
値とを一つの分析結果の中に同時に表示・記録できない
という不具合があった。
By the way, when serum proteins are tested, the fractional% of albumin, α 1 globulin, β 2 globulin, and γ globulin, and the ratio of albumin to globulin (A / G ratio) Numerical values are displayed and recorded. When the total protein amount is input, each protein concentration value is displayed and recorded by calculation. However, the conventional method of displaying and recording the analysis results could only obtain such numerical values and densitograms. In addition to this, as the data for clinical judgment, the protein concentration value of “α 1 globulin + α 2 globulin” and the ratio of “α 2 globulin / α 1 globulin” are also required. These data can be obtained by calculating based on the already obtained numerical values.
In order to make a quick clinical judgment in a test, it takes time to calculate and lacks quickness.Furthermore, the numerical value of a predetermined item and the numerical value calculated by combining these numerical values are included in one analysis result at the same time. There was a problem that it could not be displayed or recorded.

【0004】本発明は、上記不具合を解決すべく提案さ
れるもので、臨床的判断に必要なデ−タを適宜得られる
ようにした電気泳動分析結果の表示・記録方法を提供す
ることを目的としたものである。
The present invention is proposed to solve the above-mentioned problems, and an object of the present invention is to provide a method for displaying and recording an electrophoretic analysis result so that data necessary for clinical judgment can be appropriately obtained. It is what

【0005】[0005]

【課題を解決するための手段】本発明は、上記目的を達
成するために電気泳動像より得られた測定値を得る電気
泳動分析結果の表示・記録方法において、先ず電気泳動
装置の測定手段にデ−タを入力し、次に所定の計算をす
ることにより予め定められた複数項目毎の第1の測定値
を表示・記録させ、次に前記複数項目毎の測定値を臨床
的目的に応じて選定して組み合わせ計算をすることによ
り第2の測定値を表示・記録させることを特徴とした電
気泳動分析結果の表示・記録方法としたものである。
In order to achieve the above object, the present invention provides a method for displaying / recording an electrophoretic analysis result for obtaining a measurement value obtained from an electrophoretic image. By inputting data and then performing a predetermined calculation, the first measured value for each of a plurality of predetermined items is displayed and recorded, and then the measured value for each of the plurality of items is determined according to the clinical purpose. The second measurement value is displayed and recorded by selecting and performing a combination calculation, and a method for displaying and recording the result of the electrophoretic analysis is provided.

【0006】[0006]

【作用】このように第1の測定値と、第2の測定値とを
一つの分析結果として表示・記録させることができるの
で、臨床的判断に必要なデ−タを迅速に得ることができ
る。
As described above, since the first measurement value and the second measurement value can be displayed and recorded as one analysis result, the data necessary for clinical judgment can be quickly obtained. .

【0007】[0007]

【実施例】以下図面を参照しながら、本発明の実施例を
説明していく。本発明に用いる自動電気泳動装置の概要
について説明すると、支持体はセルロ−ズアセテ−ト紙
よりなるもので、ロ−ル状に巻かれたものが使用され
る。この支持体はロ−ラによって次の工程へ送られる。
ロ−ル状に巻かれた支持体は、切断機によって所定の長
さに切断される。所定の長さに切断された支持体は、湿
紙機構でペロナ−ル・ペロナ−ルソ−ダ溶液よりなる緩
衝液に浸される。緩衝液で濡らされた支持体上は、塗布
部で被検体である血清が塗布される。血清が塗布された
支持体は、電気泳動箱で通電により分画像が形成され
る。通電を終えた支持体は、染色部、脱色部、乾燥部で
染色、脱色、乾燥が行われる。次にデンシトメトリ−に
よって定量が行われるのである。定量の結果はモニタに
表示するとともに、レコ−ダに記録する。
Embodiments of the present invention will be described below with reference to the drawings. The outline of the automatic electrophoresis apparatus used in the present invention will be described. The support is made of cellulose acetate paper, which is wound in a roll shape. This support is sent to the next step by a roller.
The support wound in a roll shape is cut into a predetermined length by a cutting machine. The support cut into a predetermined length is dipped in a buffer solution composed of a peronal / peronal soda solution by a wet paper web mechanism. Serum, which is a sample, is applied to the support wetted with the buffer solution at the application unit. An image is formed on the support coated with serum by electrification in an electrophoresis box. The support that has been energized is dyed, decolorized and dried in the dyeing part, the decolorizing part and the drying part. Then, quantification is performed by densitometry. The quantitative results are displayed on the monitor and recorded on the recorder.

【0008】[0008]

【表1】 [Table 1]

【0009】デ−タに関しては、表1に示すように出力
項目N01の「依頼元コ−ド」からN060の「日付区切り記
号」まで、フォ−マットマスタ−が設定されている。こ
れらの出力項目には、「依頼元コ−ド」は「0,0」、
「患者名」は「3,2」、「報告日」は「3,4」のご
とく座標が設定されている。この各出力項目についての
デ−タが第1の測定値となるのである。次に、出力項目
としてN061以下に自由設定項目を設ける。この場合、前
記出力項目の項目番号を利用して「40+41」のごとく式
を代入して自由設定項目の出力項目とする。さらにこの
出力項目にも「12、15」のごとく座標を設定する。同様
にして自由設定項目を適宜設定していけばよい。こうし
て設けられる出力項目についてのデ−タが第2の測定値
となるのである。
As for the data, as shown in Table 1, the format master is set from "request source code" of output item N 0 1 to "date separator" of N 0 60. . In these output items, "request source code" is "0,0",
The coordinates are set as "3, 2" for "patient name" and "3, 4" for "report date". The data for each output item becomes the first measured value. Next, set freely set items below N 0 61 as output items. In this case, the item number of the output item is used to substitute an expression such as "40 + 41" as the output item of the freely set item. Further, the coordinates are set in this output item as well, such as "12,15". Similarly, free setting items may be appropriately set. The data on the output item thus provided becomes the second measured value.

【0010】上記出力項目と座標に基づいて、図1に示
すような報告書を作成するには次のようにして行う。先
ず、患者名1は出力項目N03(座標3,2)に入力し、
患者番号2は出力項目N04(座標3,3)に入力し、日
付3は出力項目N08(座標3,4)に入力し、サンプル
N04は出力項目N010(座標3,5)に入力し、A/G 比5
は出力項目N030(座標5,6)に入力し、各蛋白分画%
6は出力項目N031(座標5,7)以下の項目にそれぞれ
入力し、総蛋白量7は出力項目N021(座標0,0)に入
力し、各蛋白濃度8は出力項目N022(座標0,0)以下
の項目にそれぞれ入力する。このようにそれぞれの出力
項目に対応する座標を入力する。以上によって第1の測
定値が図1に示すように表示されることとなる。
The report as shown in FIG. 1 is prepared based on the output items and the coordinates as follows. First, input the patient name 1 into the output item N 0 3 (coordinates 3, 2),
Patient number 2 is input to output item N 0 4 (coordinates 3, 3), date 3 is input to output item N 0 8 (coordinates 3, 4), sample
N 0 4 is input to output item N 0 10 (coordinates 3, 5) and the A / G ratio is 5
Is input to the output item N 0 30 (coordinates 5 and 6), and each protein fraction%
6 is input to the output items N 0 31 (coordinates 5 and 7) and below, the total protein amount 7 is input to output item N 0 21 (coordinates 0 and 0), and each protein concentration 8 is output item N 0 Fill in the items below 22 (coordinates 0, 0). In this way, the coordinates corresponding to each output item are input. As described above, the first measured value is displayed as shown in FIG.

【0011】次に、例えば自由設定項目9「α1 グロブ
リン+α2 グロブリン」の蛋白濃度値を得るには、出力
項目N061(座標12,15)に入力する。すると、座標12,15
の位置に「α1 +α2 1.07g/dl」が記録される。他の
自由設定項目があれば同様にして入力することにより第
2の測定値が図1に示すように表示される。こうして、
各測定値の報告書が作成されることとなる。なお、10は
デンシトグラムである。以上の各測定値を記録紙にプリ
ントするためには、プリンタによって行うのであるが、
記録紙のどの位置にどのデ−タをプリントするかは印字
フォ−マットの設定によって行うようにしてある。ま
た、自由設定項目に係るデ−タを記録紙のどの位置にプ
リントするかはキ−ボ−ドによる入力によって行うよう
になっている。なお、各測定値を画面に表示させること
により、各測定値を得るようにしてもよいことはいうま
でもない。
Next, for example, in order to obtain the protein concentration value of the free setting item 9 "α 1 globulin + α 2 globulin", it is input to the output item N 0 61 (coordinates 12, 15). Then coordinates 12 and 15
“Α 1 + α 2 1.07 g / dl” is recorded at the position. If there are other free setting items, the second measurement value is displayed as shown in FIG. 1 by inputting in the same manner. Thus
A report for each measurement will be prepared. In addition, 10 is a densitogram. In order to print the above measured values on the recording paper, it is done by a printer.
Which data is printed at which position on the recording paper is set by setting the print format. Further, the position on the recording paper on which the data relating to the freely set items is to be printed is set by inputting through the keyboard. Needless to say, each measurement value may be obtained by displaying each measurement value on the screen.

【0012】[0012]

【発明の効果】以上のごとく本発明によれば、A/G 比(
アルブミン量/全グロブリン量)といった第1の測定値
に加え、特定の分画値を加え合わせた値や比を自由に設
定して得られる第2の測定値が迅速に得られるとともに
表示させることができ、臨床的に必要なデ−タが得られ
る。したがって、例えば「α1 グロブリン+α2 グロブ
リン」の蛋白濃度値により炎症性疾患や組織破壊の診断
に役立てることができ、また「α2 グロブリン/α1
ロブリン」の蛋白濃度値により血管内溶血や、蛋白漏
出、急性肝障害、ネフロ−ゼ症候群等の診断に役立てる
ことができる。
As described above, according to the present invention, the A / G ratio (
In addition to the first measurement value (albumin amount / total globulin amount), the second measurement value obtained by freely setting the value or ratio of the specific fractional values added should be quickly displayed and displayed. And clinically necessary data can be obtained. Thus, for example, it can be useful in the diagnosis of inflammatory diseases and tissue destruction due to the protein concentration value of "alpha 1 globulin + alpha 2 globulin", also intravascular hemolysis or by protein concentration values of "alpha 2 globulin / alpha 1 globulin" It can be useful for diagnosis of protein leakage, acute liver injury, nephrotic syndrome and the like.

【図面の簡単な説明】[Brief description of drawings]

【図1】本発明によって得られる報告書の一例を示した
ものである。
FIG. 1 shows an example of a report obtained by the present invention.

【符号の説明】[Explanation of symbols]

1 患者名 2 患者番号 3 日付 4 サンプルNo. 5 A/G比 6 各蛋白分画% 7 総蛋白量 8 各蛋白濃度 9 自由設定項目 10 デンシトグラム 1 Patient name 2 Patient number 3 Date 4 Sample No. 5 A / G ratio 6 Each protein fraction% 7 Total protein amount 8 Each protein concentration 9 Free setting item 10 Densitogram

Claims (1)

【特許請求の範囲】[Claims] 【請求項1】 電気泳動像より得られた電気泳動分析結
果の表示・記録方法において、 先ず電気泳動装置の測定手段にデ−タを入力し、次に所
定の計算をすることにより予め定められた複数の項目毎
の第1の測定値を表示・記録させ、次に前記複数の項目
毎の測定値を臨床的目的に応じて選定して組み合わせ計
算をすることにより第2の測定値を表示・記録させるこ
とを特徴とした電気泳動分析結果の表示・記録方法。
1. A method for displaying and recording an electrophoretic analysis result obtained from an electrophoretic image, which is determined by inputting data into a measuring means of an electrophoretic device and then performing a predetermined calculation. The second measurement value is displayed by displaying and recording the first measurement value for each of the plurality of items, and then selecting the measurement value for each of the plurality of items according to the clinical purpose and performing a combination calculation.・ Display and recording method of electrophoretic analysis results characterized by recording.
JP3238080A 1991-09-18 1991-09-18 Display/record method for result of electrophoresis analysis Pending JPH0572175A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP3238080A JPH0572175A (en) 1991-09-18 1991-09-18 Display/record method for result of electrophoresis analysis

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP3238080A JPH0572175A (en) 1991-09-18 1991-09-18 Display/record method for result of electrophoresis analysis

Publications (1)

Publication Number Publication Date
JPH0572175A true JPH0572175A (en) 1993-03-23

Family

ID=17024862

Family Applications (1)

Application Number Title Priority Date Filing Date
JP3238080A Pending JPH0572175A (en) 1991-09-18 1991-09-18 Display/record method for result of electrophoresis analysis

Country Status (1)

Country Link
JP (1) JPH0572175A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6416849B2 (en) 1999-03-03 2002-07-09 International Business Machines Corporation Method and structure to reduce low force pin pull failures in ceramic substrates

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6416849B2 (en) 1999-03-03 2002-07-09 International Business Machines Corporation Method and structure to reduce low force pin pull failures in ceramic substrates

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