JPS59145967A - Method and device for measuring information on internal respiration by automatic analysis - Google Patents
Method and device for measuring information on internal respiration by automatic analysisInfo
- Publication number
- JPS59145967A JPS59145967A JP58005791A JP579183A JPS59145967A JP S59145967 A JPS59145967 A JP S59145967A JP 58005791 A JP58005791 A JP 58005791A JP 579183 A JP579183 A JP 579183A JP S59145967 A JPS59145967 A JP S59145967A
- Authority
- JP
- Japan
- Prior art keywords
- blood
- oxygen
- information
- internal
- information processing
- 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.)
- Granted
Links
- 238000000034 method Methods 0.000 title claims abstract description 40
- 238000004458 analytical method Methods 0.000 title claims abstract description 12
- 230000029058 respiratory gaseous exchange Effects 0.000 title claims abstract description 7
- 239000008280 blood Substances 0.000 claims abstract description 47
- 210000004369 blood Anatomy 0.000 claims abstract description 47
- 229910052760 oxygen Inorganic materials 0.000 claims abstract description 27
- 239000001301 oxygen Substances 0.000 claims abstract description 27
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims abstract description 25
- 239000007789 gas Substances 0.000 claims abstract description 13
- 230000010365 information processing Effects 0.000 claims abstract description 13
- 102000001554 Hemoglobins Human genes 0.000 claims abstract description 10
- 108010054147 Hemoglobins Proteins 0.000 claims abstract description 10
- BVKZGUZCCUSVTD-UHFFFAOYSA-M Bicarbonate Chemical compound OC([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-M 0.000 claims abstract description 3
- 238000005259 measurement Methods 0.000 claims description 14
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 claims description 8
- 229910002092 carbon dioxide Inorganic materials 0.000 claims description 4
- 239000001569 carbon dioxide Substances 0.000 claims description 4
- 210000004072 lung Anatomy 0.000 claims description 4
- 239000002253 acid Substances 0.000 claims description 3
- 238000009825 accumulation Methods 0.000 claims description 2
- 238000009792 diffusion process Methods 0.000 claims description 2
- 102000004190 Enzymes Human genes 0.000 claims 1
- 108090000790 Enzymes Proteins 0.000 claims 1
- 238000004159 blood analysis Methods 0.000 claims 1
- GPRLSGONYQIRFK-UHFFFAOYSA-N hydron Chemical compound [H+] GPRLSGONYQIRFK-UHFFFAOYSA-N 0.000 claims 1
- 238000001727 in vivo Methods 0.000 claims 1
- 238000012545 processing Methods 0.000 abstract description 3
- 238000010586 diagram Methods 0.000 description 7
- 230000006870 function Effects 0.000 description 7
- 210000003462 vein Anatomy 0.000 description 7
- 210000001367 artery Anatomy 0.000 description 5
- 230000036760 body temperature Effects 0.000 description 4
- 238000004364 calculation method Methods 0.000 description 4
- 238000000691 measurement method Methods 0.000 description 3
- 101100243025 Arabidopsis thaliana PCO2 gene Proteins 0.000 description 2
- 238000004868 gas analysis Methods 0.000 description 2
- 229910052739 hydrogen Inorganic materials 0.000 description 2
- 239000004575 stone Substances 0.000 description 2
- 206010011878 Deafness Diseases 0.000 description 1
- MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 description 1
- 101100444028 Drosophila melanogaster Dso2 gene Proteins 0.000 description 1
- 102100021102 Hyaluronidase PH-20 Human genes 0.000 description 1
- 241001465754 Metazoa Species 0.000 description 1
- 101150055528 SPAM1 gene Proteins 0.000 description 1
- 208000007502 anemia Diseases 0.000 description 1
- 238000011888 autopsy Methods 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 238000012937 correction Methods 0.000 description 1
- 231100000895 deafness Toxicity 0.000 description 1
- 229910001882 dioxygen Inorganic materials 0.000 description 1
- 201000010099 disease Diseases 0.000 description 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 1
- 238000010494 dissociation reaction Methods 0.000 description 1
- 230000005593 dissociations Effects 0.000 description 1
- 238000004880 explosion Methods 0.000 description 1
- 238000003306 harvesting Methods 0.000 description 1
- 208000016354 hearing loss disease Diseases 0.000 description 1
- 208000015181 infectious disease Diseases 0.000 description 1
- 238000001802 infusion Methods 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 150000002926 oxygen Chemical class 0.000 description 1
- 238000002640 oxygen therapy Methods 0.000 description 1
- -1 perform nidometry Substances 0.000 description 1
- 230000000241 respiratory effect Effects 0.000 description 1
- 230000005070 ripening Effects 0.000 description 1
- 235000015170 shellfish Nutrition 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical class O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N33/00—Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
- G01N33/48—Biological material, e.g. blood, urine; Haemocytometers
- G01N33/483—Physical analysis of biological material
- G01N33/487—Physical analysis of biological material of liquid biological material
- G01N33/49—Blood
- G01N33/492—Determining multiple analytes
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Biomedical Technology (AREA)
- Chemical & Material Sciences (AREA)
- Hematology (AREA)
- Physics & Mathematics (AREA)
- Analytical Chemistry (AREA)
- Biochemistry (AREA)
- Urology & Nephrology (AREA)
- Ecology (AREA)
- Food Science & Technology (AREA)
- Medicinal Chemistry (AREA)
- Biophysics (AREA)
- Molecular Biology (AREA)
- General Health & Medical Sciences (AREA)
- General Physics & Mathematics (AREA)
- Immunology (AREA)
- Pathology (AREA)
- Investigating Or Analysing Biological Materials (AREA)
- Automatic Analysis And Handling Materials Therefor (AREA)
- Measurement Of The Respiration, Hearing Ability, Form, And Blood Characteristics Of Living Organisms (AREA)
Abstract
Description
【発明の詳細な説明】
この)発明は人間の血液(各種動物の血液もこhこ準す
る)を科学的に測定解析し、診断者(二対して適切な判
断用情報を提供するための肺及び血液ζ1よる内呼吸情
報の自動解析装置及び方法(二関するものである。[Detailed Description of the Invention] This invention is a method for scientifically measuring and analyzing human blood (similar to the blood of various animals), and providing diagnostic information to diagnosticians (2). and an automatic analysis device and method for internal respiration information based on blood ζ1 (these two are related).
血液中最も重装とされる成分のヘモグロビン、(Hb
)は肺(二よりて受殴った酸素を生体内の各組織へ運搬
する目的で存在する。しかしこのHbは肺(二よって結
合した酸素を組織ですべて放出することはできず、正常
人でも25〜30係程度しか放出することができない。Hemoglobin, the most heavily loaded component in blood (Hb
) exist for the purpose of transporting the oxygen that is received by the lungs (2) to each tissue in the living body. However, this Hb cannot be released completely by the tissues that have been bound by the lungs (2), and even in normal people. Only about 25 to 30 units can be released.
このHb対酸素の結合及び放出能力は個々患者のHb
自体の能力、血液のpH1炭酸ガス量、体温等(二よっ
て大幅(1変化する。こり″能力を調べる手法は一般【
二血液の02分圧と係02Hb又は02 含量の関係に
よって表現gtt%縦軸にヘモグロビンの酸素含有係の
φ02T(b横綱(二酸素分圧P o zをとり、P
O2をゼロから150mm )Ig 程1屍まで変化さ
せると第1図1(=破線(イ)、実線(ロ)および一点
鎖線(ハ)で示す様な特有のS字状力jえ
一ブを呈する。これffi I(b のr俊素平衡曲ぎ
(OEC)又はHb の酸礪解離曲、J(01)C)
と称し、組織側が維持している最低必要酸素分圧で
どの程度の酸素計を放出することができるかを仰る為(
二(グめて重要な指標となるっ
逼
今こ\でh朋の保存血や@度の喫煙者から輸抑を受けた
患者の俤(二OEC全体が左傾している、即ち、第1図
の破線(イ)のような場合、低い1〕o2テも多くのH
b が酸fヒさF?、るため02結合能カは高いが、組
織側のP o 2程度では漬がしか02 を放出でき
ず、血中の酸素分出は充分高くともこの酸素を利用でき
ないため、一般的酸素療法は不可能となる。一方このO
ECが右傾しでいろ、即ちAL1図の(ハ)f二定j一
様な場合は、理論的f劇Mjでの02結合力が低−トす
ることベニなるが、肺(ユおける02分圧は10011
1g稈度と充分高い為0□結合C二はほとんど影iBを
受けず、組織側の1)o2が比較的(1高くとも充分な
酸素を放出することができ、多少の貧血状聾や呼吸疾患
等(二よって動脈血酸素分圧が低くとも充分生活できる
ことを意味する。しかしこの様(二〇ECの左傾、右傾
は数値的でないなめ表現が困難であるうそこで一般的(
二は当該OECカーブ上で、%02Hb50%N″一対
応するP o 2すなわち全Hbの50チが02Hbl
二なる為【二必快な02分圧で表現し、psoと記載す
ること(二なっている。This Hb-to-oxygen binding and release capacity is determined by the individual patient's ability to bind and release Hb to oxygen.
own ability, blood pH, amount of carbon dioxide, body temperature, etc.
2 Expressed by the relationship between the 02 partial pressure of blood and the 02 Hb or 02 content gtt% The vertical axis is the oxygen content of hemoglobin φ02T (b Yokozuna (taking the dioxygen partial pressure P o z, P
When O2 is changed from zero to 150 mm) Ig, a unique S-shaped force as shown in Figure 1 (= broken line (A), solid line (B), and dashed line (C)) is generated. This is ffi I (r-element equilibrium curve (OEC) of b or acid dissociation curve of Hb, J(01)C)
In order to tell how much oxygen meter can be released at the minimum required oxygen partial pressure maintained by the tissue (
2 (This is a very important indicator.The number of patients receiving infusions from a friend's stored blood or a smoker at this time) (2) The entire OEC is tilted to the left, i.e. In a case like the broken line (A) in the figure, even a low 1] o2 temperature can cause a lot of H
b is acid f hisa F? , the 02 binding capacity is high, but if the tissue side P o 2 is around, only pickled 02 can be released, and even if the oxygen content in the blood is high enough, this oxygen cannot be utilized, so general oxygen therapy is It becomes impossible. On the other hand, this O
If EC is tilted to the right, that is, if (c) f constant j in the AL1 diagram is uniform, the 02 bonding force in the theoretical f-play Mj will be low, but the 02 minute in the lung (Y) The pressure is 10011
Since the culm degree is sufficiently high at 1g, the 0□ bond C2 is hardly affected by iB, and even if the 1) O2 on the tissue side is relatively (1) high, sufficient oxygen can be released, causing some anemia-like deafness and respiratory problems. Diseases, etc. (2) means that it is possible to live well even with a low arterial blood oxygen partial pressure.
2 is on the OEC curve, %02Hb50%N'' - the corresponding P o 2, that is, 50ch of the total Hb is 02Hbl
Because it is two, it is expressed as 02 partial pressure and written as pso (it is two.
この−DEC及びP5oは前述の通りHb 自体の個
々の機能のみならず、血液のpH2炭酸ガス分圧(PC
O2)、体温等C二よって大巾(1変化する為(二従来
はこれらの条P+をpHニア、4、PCO2:40龍W
。As mentioned above, this -DEC and P5o are important not only for the individual functions of Hb itself, but also for the blood pH2 carbon dioxide partial pressure (PC
O2), body temperature etc. C2 changes by 1 (2) Conventionally, these articles P+ are pH near, 4, PCO2: 40 Dragon W
.
体温:37℃の標準条件(二定めた場合のflEc、P
5oを求めて、 Hb 自体の02運搬能のみを検討
するのが通例であった。しかし個々の患者はこの条f′
+iMりでしまないため、生体内でけかな11異った能
力をもっていることζ:なり、■Ib 自体り) )葎
f<旨が判明しても、実際の輸血、呼吸管理の臨床く二
おいて、これらのデータをそのせ\用いることができな
いなど実用的ではなかったつ
そこでl(b 自体の機能を検討するため従来直り標準
条件(二補正した場合の0EC(IJ、千correc
tedOECとよぶ−)P2Oと共に実際の虫目・榮注
−ト(−おけるその筐\の0EIII)、 (以下ac
tual OE Cとよぶ)P5oを”iJ比させ、更
(二当該血液での曲論的酸素運搬可能ht、(Sta
−vDo2)、生体内の動、静脈血間で実際(=消費さ
itている酸素3 (a−vl)o 2 )、肺胞内外
で行なわ)する02のガス拡散較差(A−aDo 2
) %肺胞パイ・やス率の指標5hunt率等、実際の
臨床管理(二屯卯な内呼吸1′1イ報を少itの血液で
短時間(−何時でも誰でも正確(1得られる新しい測定
器材と測足法が緊急C二必曹であると鱈えられる(二到
った。Body temperature: standard conditions of 37°C (flEc, P for two specified cases)
In determining 5o, it was customary to consider only the 02-carrying capacity of Hb itself. However, individual patients
+iM Even if it is determined that the body has 11 different abilities in order to prevent the infection from occurring due to However, in order to examine the function of l(b) itself, it was not practical to use these data.
It is called tedOEC-) P2O and the actual bug eye Ei Note (-0EIII of that box in -), (hereinafter ac
tual OE
-vDo2), the actual gas diffusion gradient of 02 (A-aDo2) between the active and venous blood in the living body (=oxygen consumed (a-vl)o2), carried out inside and outside the alveoli).
) Actual clinical management, such as % alveolar pi/mass rate index 5hunt rate, etc. The new measuring equipment and foot measurement method are said to be an emergency.
そこで、この発明(二立ち到ったわけであるが、この発
明の詳細を述べる(二先立ち、従来用いられて来たHK
倒及び方法の櫃要を述べ、その欠点を明らかにすること
\する。Therefore, we will describe the details of this invention (which we have just arrived at).
I will explain the main points of the method and methods and clarify their shortcomings.
41211て、従来用いられて来た測定法の第] 6;
t jt トノメ)・り一法”である。こttは最も基
本的手法である。pIJち、Pco を40 mm
、I(g、−Po2を0〜1501!lllHg の
範囲で%40〜50種類の煙準ガス金用意し、そ)tぞ
れのガス濃度で血液を・トノメトリーし、血液ガス分析
装咬とオキシ、ノークでP o 2対、S O2’Z石
PインIf実測するうこの値はpH1二よって変化ずろ
ためa11式て補市をした」−1Y軸上C二、5o2k
、X軸上”Po2’tとり、40〜5071?インドヲ
測定すね、げ、OECが画ける。このOE Cから5o
50係(二対応するP o 2をP、。とfイ)。こり
〕時S O250%の点がνこIllじ11ろ確率は少
ないため、その間−1]ill 式Q曲、彷j適合でS
O25,0% (一対応するPoを穫」」する75%
P Q 2 、 SO2’2”夫々tOg変換を行な
い、直線【二近づけてから直線1司帰の手段を・用いて
、5o50%(二対応するPo を求め、P5oとす2
る。この場合全面液歇けlO〜20釦で、P5oのみの
値を求める場合でも%50Cの血液を必要とし、第2の
方法’t ” U &法″である) P c o 2
’ 40 耶Hg、P O2’ (Jと、同じ< Pc
o2:40 pmrig 、 Po2’200〜300
閥f1gの2種類のガスを準備し、そり、ぞれ〜ニドツ
メトリーさり、た血液の同惜庖嫌気的C二混合し、その
時のPo2を測定してP 50とする方法でちる。これ
けP5Qのみの太まがなで直を得ろ時(−利用さttて
いるが、熟練ヶ要し5精変も良くないっ)屍84のセル
(二02電倖を接続し、568rm+ の信号を48
準として、560 nrlの信号の変fヒをY軸+二、
0□ 分圧の変化全X@どなるようCXYレコーダ(二
接続し、血0.を入りたセル(二o2又は、N2をバフ
゛リングさせ、これ−二よって℃ゴヒするPo2と0゜
)Ib(D斐fヒ全描かげイン、この方法(二はセルの
中の血液にバンファーケ入りてpHを7.4(二1呆ク
タイブと、全面で行なうタイプとがあるが、全面で?テ
なうタイfは測定中血液のpHが変化するため正確ナカ
ーブとp r、oh”得らり、(=くい。又・ぐツファ
ーを入れるタイプはバッファーの精変+1.1って町な
りの変化を受け、史(二軸IF及び測定じ町t「りの時
間を要する等種々の間i、qツノ玉あるついず仇のタイ
プも測定中σ)02M%のドリフトの影響は耕けらね7
ず、キャリブレーションその曲で1倹体C二ついては1
時j用18L上の時間を要するっそこで此り方法も臨床
で’;t l”Lどんど利用さhていt(いっ
第4の方法は、数点のS on ’一対ずろP n 2
の実測によって、主と17で計算式【−につてOE C
、P 5(1を求める手法である。この手法(−は式の
種類(二上って次の4種類がある。即ち、
こ帆は!鴬もポピユラーな手l左であるが、卯弐ケその
斗ま甲いたのでは、SO2,50爆附近を合せろ(子(
二〇を屑?r、ことはできるが、SO□のに逃い点、低
い点では町なりの誤差ケ生ずるためこれらの実測1 の
「范をもと・二O5ofd: Ill陣した場合、何1
1、も町なりのマイナス、i0差を生ずる。41211, measurement methods that have been used conventionally] 6;
This is the most basic method.
, I(g, -Po2 in the range of 0 to 1501!lllHg) Prepare 40 to 50 types of smoke-like gases, perform tonometry on the blood at each gas concentration, and use a blood gas analysis instrument. Oxygen, Nork P o 2 vs. S O 2 'Z stone P in If the actual value of the stone P in will vary depending on the pH 12, so we supplemented it using the formula a11'-1 C2 on the Y axis, 5o2k
, take "Po2't" on the X axis, and measure 40 to 5071?
Section 50 (two corresponding P o 2 P,. and f i). Since the probability that the point of S O250% is ν is small at the time of −1]ill, the S
O25,0% (75% to "harvest the corresponding Po")
Perform tOg conversion on each of P Q 2 and SO2'2'', bring the straight line [2 closer together, and then use the method of recursive line 1 to find the corresponding Po of 5o50% (2, and set it as P5o2. In this case, the entire surface With a liquid interval of 10 ~ 20 buttons, even when determining the value of P5o only, %50C of blood is required, and the second method is the ``U &method'') P co 2
' 40 YHg, P O2' (same as J < Pc
o2:40pmrig, Po2'200~300
Prepare two types of gases, perform nidometry, and mix the same and anaerobic gases of blood, measure the Po2 at that time, and set it as P50. When you get a straight line with P5Q only (I use it, but it requires skill and 5 Seihen is not good) Corpse 84 cell (connect 202 electric, 568rm+) signal 48
As a standard, change f of the signal of 560 nrl on the Y axis + 2,
0 □ Change in partial pressure All This method (2) enters the blood inside the cell and adjusts the pH to 7.4 (21) There are two types: one that is done on the entire surface, and one that is done on the entire surface. Since the pH of the blood changes during the measurement, it is difficult to obtain an accurate nacurb and pr, oh. The influence of the drift of 02M% cannot be investigated.7
First, calibration: 1 body C and 2 in that song is 1
This method takes over 18L of time, so this method is also used in clinical practice.
Based on actual measurements, the calculation formula [-OE C
, P 5 (This is a method to find 1. This method (- is the type of expression (Fukui) There are four types as follows. Now that you've reached that point, let's put together a SO2, 50 explosion.
Waste twenty? r, it is possible to do this, but at the low points and low points of SO□, there will be errors depending on the town, so based on these actual measurements 1.
1 also causes a town-specific minus, i0 difference.
四メ量体であるR間のHbのHb+no2−!Hb(o
2)nをうまく説明する為(二考えられた式であり、4
種のAdair係数を必要とする。即ち、4ポイント以
上の実測プ′−夕から求める為、精変的(二は±1.2
チと、池の方法(ニルべて高いが、前述した1トノメト
リー法″−一近い労力を必要とし、1算が複雑で時間が
かかるという欠点がある。Hb+no2- of Hb between R which is a tetramer! Hb(o
2) In order to explain n well (this is a formula that has been considered twice, and 4
Requires the Adair coefficient of the species. In other words, since it is calculated from actual measured plots of 4 points or more, it is highly variable (2 is ±1.2
Second, Ike's method (albeit more expensive than the one-tonometry method mentioned above) has the disadvantage that it requires almost as much effort, and the calculations are complex and time-consuming.
(c)、LutsO式
Hill 式の変形で動脈血の実測点を必ず通過させ
ることはできるが、P、、Oは用11式と同様な誤差を
生ずるという欠点があるっ
(d)、Aberman 0式
標準カーブと実測点との差を比例配分的に求めて、カー
ブを描く方法である。この方法は、啄めて、標準的なカ
ーブには有効であるが、全カーブを描くことができない
、動脈血ポイントを通過させることができないなどで、
一般(二は使われてし)ない。(c), LutsO formula Although it is possible to always pass the actual measurement point of arterial blood by modifying the Hill formula, P,,O has the disadvantage that it causes the same error as Equation 11 (d), Aberman 0 formula This is a method of drawing a curve by calculating the difference between the standard curve and the actual measurement points in a proportional manner. This method is effective for standard curves, but it cannot draw the entire curve, it cannot pass the arterial blood point, etc.
Generally (two is not used).
以上【二概観したようζ二、従来の内呼及情報の解析、
特(二Hbの酸素運搬能力を調査する装置乃至方法とし
ては種々のものが開発されCし1ろう−、イ弓りも操作
が面倒であII、l検オ・のデータを得る為には少くと
も1時間から手法(−よって6t 6〜8時間1fr要
するなど多大の時間を要し、特(−輸血を・必要とする
ような臨床現場では緊急性カー高1/)ため、全く利用
することが出来ず、専ら学術釣具1未の対象として用い
られている(1過ぎなかった。又仮IJ(−簡易法で測
定時間が短縮さhたとしても、イ言頼性と積度の点で所
要のし4ルに達しCI/)な(すFtげ、臨床的(二安
心して使用することは出来なし)のであって、従来の何
れの方法でも、臨床的ζ二利用町a目を判定される測定
装置や測定方法は見当らなめ・つたっ
この発明は2以上述べた種々の困難を克服して、正確く
二しかも短時間C二所要のデータを提供する装置及び方
法を得ることを目的として為されたものであるっ
以下この発明(二ついて一実施例を図面−二よって詳し
く説明する。As mentioned above [2] ζ2, analysis of conventional internal reference information,
In particular, various devices and methods have been developed to investigate the oxygen carrying capacity of Hb, but the operation of the bow is cumbersome, and it is difficult to obtain the data for the test. The method requires at least 1 hour (- Therefore, 6 tons, 6 to 8 hours, 1 fr, etc.), and it requires a lot of time, especially (- In clinical settings where blood transfusion is required, the urgency is high), so it is not used at all. Therefore, it is used exclusively as a subject for academic fishing gear (not more than 1).Also, even if the measurement time is shortened by the provisional IJ (-) simple method, it is difficult to measure reliability and accumulation. However, it is not possible to use it with confidence in a clinical setting. Tsutakko's invention aims to overcome the various difficulties mentioned above and to obtain a device and method that provide the required data accurately and in a short time. This invention has been made for this purpose.Hereinafter, one embodiment of the present invention will be described in detail with reference to Drawing 2.
先づけしめ(−1この実施例C二おいて実用した血液ガ
ス分析装置(以下A装置と呼称する)の構造と機能及び
COオキシメータ(以下B装置と呼称する)の構造と機
能を概説し、更(二情報処理装置、(L:J、下C装置
と呼称する)へのデータの導入方法(二ついて説明する
。Preface (-1) Outline the structure and function of the blood gas analyzer (hereinafter referred to as device A) and the structure and function of the CO oximeter (hereinafter referred to as device B) that were put into practical use in this Example C2. , and a method of introducing data into the second information processing device (L:J, referred to as C device below).
A装置:血液ガス分析装置(ILシステム、1303m
、)
この装置は血液中の酸素分圧、 Co□分圧、 pH5
重炭酸水素イオンmco3.酸塩基平衡能力の指標十B
E、 Co2含量、その池を同時(=37°±0.1℃
で分析し、37℃での値と指定された7の者の(*温で
補正された値の2種類を同時(−出力することのできる
装置である。A device: Blood gas analyzer (IL system, 1303m
,) This device measures oxygen partial pressure, Co□ partial pressure, and pH5 in blood.
bicarbonate ion mco3. Index of acid-base balance ability 10B
E, Co2 content, the pond at the same time (=37°±0.1℃
It is a device that can simultaneously output two types of values: the value at 37°C and the value corrected by the temperature of the specified 7 people.
B装置二〇〇オキシメータ(IL282型)この装置は
血液中の02Hb 、 C0Hb 、λ4etHb。B Device 200 Oximeter (IL282 model) This device measures 02Hb, C0Hb, λ4etHb in blood.
又はこれらのH,bを合計したTHb (トータルヘモ
グロビン)と02含量を300μtの僅少な血液を用い
て1分間以内(二同時(=分析する装置であるっC装置
:11す報処理装ft (If 800 Mof、30
、沖電気製)
この装置はいわゆるミニコンピユータで、280BCP
Uを用い、主記憶写量128KBを標準装置とし、CR
T、フ0リンター、■BMFJ準タイプのダブルフロッ
ピーディスクを保有する標準的オール。イン、タイプの
情報処+!J! t4置である。Alternatively, THb (total hemoglobin), which is the sum of these H and b, and 02 content can be measured within 1 minute using a small amount of blood of 300 μt (two at the same time). If 800 Mof, 30
(manufactured by Oki Electric) This device is a so-called mini computer, with 280 BCP.
U, main memory copy size 128KB is used as standard equipment, CR
T, Flinter, ■BMFJ Standard oar with semi-type double floppy disk. In, type information place +! J! It is at t4 position.
上述のA装置及びB装置【二よって分析された各値を、
定められた型の情報にリアルタイムさせるためC装置τ
二対してRS−232CのインターフェースカードD
を挿入し、定められた手111−従って処理を行なわせ
ろ。この場合の操作子+1Fjは逐次CRT上C二表示
さtするしくみとなっているので、その指示(二従って
操作ケ進めるっ
この発明の要点は既成のA装置、B装置及びC装置を一
般的標準のインターフェースカードDを用いて一つのシ
ステムとして結びつけることによつで以下−二述べろ9
丁も理方法を測定法として考え出したことと相まって全
く新しい機能elすシステムとその1吏田方法を確立し
たことである、そこで次(二上述のA装置4、B装置、
C装置及びD8−ドを用いて、内呼及情報を測定する処
四方法(二ついて説明するっ
第2図は、この発明の一実施例を示すブロック図であり
、第3図は、この実施例で1吏用した情報処理装置の内
部機能を示すブロック図であるう図(二おいて、(1)
は、A装置、(2)はB装置、(3)はC装置、(4)
はDカードを示す。Each value analyzed by the above-mentioned device A and device B [2] is
C device τ to provide real-time information of a defined type
RS-232C interface card D
Insert and perform the prescribed move 111--accordingly. In this case, the operator +1Fj is sequentially displayed on the CRT. By linking as a single system using a standard interface card D, the following two statements can be made.9
Coupled with devising the method as a measuring method, we established a system with completely new functions and the 1.
Four methods of measuring internal call information using a C device and a D8-card (two methods will be explained) FIG. 2 is a block diagram showing an embodiment of the present invention, and FIG. Fig. 1 is a block diagram showing the internal functions of the information processing device used in the embodiment (Fig.
is A device, (2) is B device, (3) is C device, (4)
indicates a D card.
Dカード(4)はRS232Cインターフ−−スカート
である。さてここでこれ等の装置の組合せとしてのこの
システムの1吏用法(二ついて次に述べろっ(α)静脈
血一点のみでの処理法っ
B装置(2)で求めら江た静脈血の爾因子(02Hb、
COHb. Me t. Hb、)をもとく−還元Hb
. (Red Hb )を求め、C0Hb、 Me t
Hb等02運搬(二対して無効なT(b e除外した
有効Hb■みての%02Hb比を求め、実測S02とす
るっ
Red、)1[b−100((()zト1b)”(CX
))To)”(Met)To)) =・・・・=・■
実測力2=(02Hb/Re番トリ2Hb)xloo
・・・・−・・・・・・・・・−・・・■このSO□
をXA′座標のY軸上C二とりA装置によって得ら江る
患者体(it二よって補正さbたPozをX軸上口とれ
ば、当該血液の生体条件下ζ二おける酸素平衡曲線(O
EC)上の一点が定まる。D card (4) is an RS232C interface skirt. Now, let's talk about how to use this system as a combination of these devices. Factor (02Hb,
COHb. Met. Hb,) - reduced Hb
.. (Red Hb), C0Hb, Met
Hb, etc. 02 transport (2 versus invalid T (b e Excluding effective Hb CX
))To)”(Met)To)) =・・・・=・■
Actual force 2 = (02Hb/Re number bird 2Hb)xlooo
・・・・・・-・・・・・・・・・-・・・■This SO□
If we take Poz, which is corrected by the patient's body (obtained by the A device) on the Y axis of the O
EC) One point above is determined.
この一点をもと【二、
■)Ti110式(−あてはめ、nを2.7前後と定め
れば、一応生体φ件下のopc+二近いカーブを描くこ
とはできる。しかし従来から広く知ら沈ている様(二、
この方法では実測点として50チ附近のSO2があたえ
ら比たときしか正確なP5o を求めることができず、
又5()係附近のSO2が実測として与えられても、こ
の点から上記の弐〇)で、全体のoh;c’を求めた場
合カーブの両端それぞれ’/3け可なりの誤差を生ずる
。Based on this point, [2, There seems to be (2,
With this method, accurate P5o can only be obtained by comparing SO2 around 50 cm as an actual measurement point.
Also, even if the SO2 in the vicinity of 5 () is given as an actual measurement, if the overall oh; .
実際の静脈皿SO2の範囲は20〜80チと広いため上
記の式■をその1ま用いてPs[+や0FJCk求めて
も誤差の確率が高く、晩生の現場で利用することは不可
能である。そこで、この発明では%C0Hb−[iiよ
って修飾されるSO?対nの関係式を定めた。このS0
7対nの 関係式を用いて静脈+1[を実測値のSO2
とC01(bの値によって自動的にnい価が変化するH
il1式の新しい計算法全考案した。この方法に基いて
先のXY座標上に求めた静脈1出生体条件下の一点から
80250%に対応するPo2 値即ち、実態のP5o
?求めるとP5o=exp(log(K)/n)・・・
・−・・−■カーブ全体については
の式を用いて5O20,l−100%を任意の間(部で
与えられたSO2に対応するPO2対nの関係式を用い
る。Ps[1は上記で求められたPso値を用いる。The actual range of venous dish SO2 is wide, from 20 to 80 cm, so even if you use just one of the above equations to calculate Ps[+ and 0FJCk, there is a high probability of error, and it is impossible to use it in the field of late ripening. be. Therefore, in this invention, SO? modified by %C0Hb-[ii? A relational expression for pair n was determined. This S0
Using the relational expression of 7 vs.
and C01 (H whose value changes automatically depending on the value of b)
A new calculation method for the il1 formula was devised. Based on this method, the Po2 value corresponding to 80250% from the point found on the XY coordinates of the vein 1 under the birth condition, that is, the actual P5o
? When calculated, P5o=exp(log(K)/n)...
・-・・-■ For the entire curve, use the formula to set 5O20,l-100% between arbitrary intervals (use the relational formula of PO2 vs. n corresponding to SO2 given in part.Ps[1 is the above) The obtained Pso value is used.
この様な手法でXYJ!4!標上に求められたすべての
SO2対PO2の値全グロットすれば正確なactw!
−0JI;C(i−描くことができる。XYJ with this kind of method! 4! If you plot all SO2 vs. PO2 values determined at altitude, you will get accurate actw!
-0JI;C(i-Can be drawn.
更に患者体温やPL(、PCO2で影l#ケ受けないY
lb自体の榛能を解析するために1従来通り定めらtl
、た条件(PH;7.4、PCO240mmJg体淵3
7°(−2での0ICC)でcorrectcd OE
C’fr求めなけれはならない。In addition, the patient temperature and PL (, PCO2 are not affected by Y)
In order to analyze the performance of the lb itself, the conventionally determined tl
, conditions (PH; 7.4, PCO240mmJg body depth 3
correctcd OE at 7° (0ICC at -2)
We must find C'fr.
狐
そこでA @ 置mの血液ガス分析装置から37 Cで
求められた各個を導入する。併f、 PH1PC(hは
定められた条件内にあるとは限らないため、下式をHh
て補正する。There, each individual determined by 37C is introduced from the blood gas analyzer at A@m. Combined with f, PH1PC (h is not necessarily within the specified conditions, so the following formula is changed to Hh
Correct it.
補正後のPO2=実測PO2X rxp +o(0,4
8x(nトi−7,4)−0,1JOB噛IC)・・・
・・・・■この祁j正をfしたPO2とactual
P!+11計算時に用いた実mll SO2k XY座
標にフ0ロットすればcorrectedolDCの一
点が定まる。この点るもとに上記ActualOEC,
Ps n f求めたと同一の手法でcorrect、e
dOECXPso ′に求める。PO2 after correction = Actual PO2X rxp +o(0,4
8x (ntoi-7,4)-0,1 JOB bite IC)...
・・・・■PO2 and actual
P! By plotting the actual mll SO2k XY coordinates used in +11 calculation, one point of correctedol DC is determined. Based on this point, the above ActualOEC,
Correct, e using the same method as Ps n f.
dOECXPso'.
次にこのcorrected OECfもとに、動脈(
(190rrmhg。Next, based on this corrected OECf, the artery (
(190 rrmhg.
静脈ffn 40nmh gの一般的条件下において当
該血液では理論的にどの程度の酸素を放出可能がを表す
St’a−VDo2’r
※3
Stk−VDo2=1.39 x (Hbx%Ds O
2/ ]、 (J O)+0.155 (7)で求める
。こ\で※1.2.3.4、は次のとおり。St'a-VDo2'r *3 Stk-VDo2=1.39 x (Hbx%Ds O
2/], (J O)+0.155 (7). Ko\de*1.2.3.4 are as follows.
※j:而#面00CC当り1gのH,bが存在するとき
、理論的に結合できうる02i/ec※2:有効Hbウ
ドIb x(l(%COHb−f−Me tHb )/
1.00(即位は g7100c c ) ・・
・・・・・・−■* 3 : %Dso2=(Po29
0mmhg K、対する%S02〕−(po 24f1
mmhgに対応する%502)・・・・・・・■
* 4 : (PO290mmhgiCおける溶存酸素
1−(Po 240mmhg VCおける溶存酸素)
−・・・(単位1jcc)・・・・・・・・・・・−・
・・・・・・・・・・・・・・・・・・・・・・[相]
これで静脈+rlLのみでのルーチンデークー解析ハ完
了するが、目的に応じて5O275%に対応するPo2
、即ちP75をもP2Oと同様手法で求めることができ
る。これらすべてのデータはすべて、C装置の情報処理
装置のCRT上に表示され、 入力されたデータと共に
ハードコピーにも作られる。*j: When there is 1g of H, b per surface 00CC, it is theoretically possible to combine 02i/ec *2: Effective Hb Ib x (l(%COHb-f-Me tHb)/
1.00 (enthronement was g7100cc)...
......-■*3: %Dso2=(Po29
0mmhg K, %S02] - (po 24f1
%502 corresponding to mmhg)...■ *4: (Dissolved oxygen in PO290mmhgiC 1-(Po240mmhg Dissolved oxygen in VC)
−・・・(Unit: 1jcc)・・・・・・・・・・・・・−・
······················[phase]
This completes the routine decoup analysis using only veins + rlL, but depending on the purpose, Po2 corresponding to 5O275% can be used.
, that is, P75 can also be determined using the same method as P2O. All these data are displayed on the CRT of the information processing device of the C device, and are also made into hard copies along with the input data.
なおこれらすべてのデータ全データ処理契商内に蓄積す
る必要がある場合は、指示に基いて記憶蓄積され、何時
でも、測定時と同様の状態でCR1表示と、・・−トコ
ピーと金得ることができる。If all of this data needs to be stored within the data processing contract, it will be stored in memory based on the instructions, and CR1 will be displayed at any time in the same condition as at the time of measurement. I can do it.
(#l Actual a−vDo2、A−aDo
2.5hunt率等を得るために静脈[111と共に
動脈+111 eも測定する方法。(#l Actual a-vDo2, A-aDo
2.5 A method of measuring artery +111 e along with vein [111] to obtain hunt rate, etc.
A装置(11及びB装置(2)によって分析された静脈
It’ll情報全−fAC装置内に記憶蓄積させ、次に
、C装置のCRT上の指示に従い動脈+m r A装置
及びB装置に導入する1、この動脈+m情報がC装置に
導入されると、さきに蓄積されていた静脈I11の情報
と組合わされ、静脈rotのみの情報処理の場合と同様
の手II k踏んでRCt 11 Fl l OECと
P!10 % correctedQE(:とPbo、
St’a=vDo 2 k求めるが、コノ場合静脈面ポ
イントと動脈+m yjPインドの2点が与えられてい
るため、理論的には一層高い精度ケ得ることが出来るが
、一点法と有意の差を生じていない。All the vein information analyzed by the A device (11 and B device (2)) is stored in the AC device, and then introduced into the A and B devices according to the instructions on the CRT of the C device. 1. When this artery+m information is introduced into the C device, it is combined with the previously accumulated information on the vein I11, and the same steps as in the case of information processing of only the vein rot are performed to perform RCt 11 Fl l OEC and P!10% correctedQE(: and Pbo,
St'a = vDo 2 k is calculated, but in this case, two points are given: the venous surface point and the artery + m yjP India, so theoretically higher accuracy can be obtained, but there is a significant difference from the one-point method. has not occurred.
この動、静脈面の実測データをもとにして、actua
] a−vDo2、A−af)o 2.5hunt率等
は、下記の手法によって求める。Based on this actual measurement data of the arterial and venous surfaces, actua
] a-vDo2, A-af)o 2.5hunt rate, etc. are determined by the following method.
こ\で◆5.5ao2 :動脈1fIIS□z※6.5
vO2:中心静脈1111 S o 2、秦7、PaO
・2:動脈血P02゜
※8、PVo2 °中心動脈血PO2、こ\で※9、F
i O2・吸気02%※10.BP:大気干顛hg
※貝 PH20:体温における飽1和水蒸気匝
※12、Pac02 :動脈血炭酸ガス分子、※13、
R:ガス交換率
(i) Sao 2=100%、S Q o 2=
100%のとき’jat=0.0”6”x’g−aDo
2 a−vDo 2 ×lOO”’ @(ji)SV
O2<100%のとき、
こ5で※14.5(PaO2):肺胞1111の802
尚この内呼数情報の自動解析法の中心をなす酸素平衡曲
線OEC,P5o の分析精度を最もきびしい条件で
現在最も信頼されているトノメトリー法と関
比較した場合のその相間は、
Y = 0.2481+0.9855 X・・・・・・
・・・・・・・・・・・・・・@R= 0.9865、
N=120
である。この関係は第5図に示すとおりである。Ko\de◆5.5ao2: Artery 1fIIS□z*6.5
vO2: Central vein 1111 S o 2, Qin 7, PaO
・2: Arterial blood P02° *8, PVo2 ° Central arterial blood PO2, Ko\de *9, F
i O2・Intake 02% *10. BP: atmospheric drought hg *shellfish PH20: saturated water vapor at body temperature *12, Pac02: arterial blood carbon dioxide molecules, *13,
R: Gas exchange rate (i) Sao 2 = 100%, S Q o 2 =
When 100% 'jat=0.0"6"x'g-aDo
2 a-vDo 2 ×lOO”' @(ji)SV
When O2<100%, 5*14.5 (PaO2): 802 of alveoli 1111
Furthermore, when comparing the analysis accuracy of the oxygen equilibrium curve OEC, P5o, which forms the center of the automatic analysis method for call number information, with the tonometry method, which is currently the most reliable, under the most severe conditions, the correlation is Y = 0. 2481+0.9855 X・・・・・・
・・・・・・・・・・・・・・・@R=0.9865,
N=120. This relationship is as shown in FIG.
ここでRは相関係数、Nはサンプル数をあられす。Here, R is the correlation coefficient and N is the number of samples.
0式は直線に6られし、その相関は明らかである。Equation 0 is drawn into a straight line, and the correlation is clear.
つまり98.65%の相関をもつものと認めて差支えな
いことを示している。In other words, it shows that it is safe to accept that there is a correlation of 98.65%.
以上に説明した様にこの装置及び方法を用いれば、従来
の測定法では1時間以上の長時間を敦し臨床には全く使
用不可能であったOF:、CやPbo の測定が、立
ちどころに正確に測定出来、臨床にも応用できるという
効果がある。As explained above, if this device and method are used, the measurement of OF:, C and Pbo, which conventional measurement methods require for a long time of one hour or more and is completely unusable in clinical practice, will be possible. It has the advantage that it can be measured accurately and can be applied clinically.
第1図はヘモグロビンの酸素平衡曲線OECの説明図、
第2図は、この発明の一実施例を示す装置のブロック図
、第3図はこの実施例に使用した情報処理装置の内部機
能のブロック図、第4図は、この実施例によるC RT
表示及びノ・−トコピーにプリントされる酸素平衡曲線
及びデータ表の実例、第5図は、従来のトノメトリー法
による測定結果と、この発明による測定結果との比1”
!2を示す図である。図において、
[11・・・・A装置:血液ガス分析装楢、(2)−・
・・・・B装置:COオキシメータ、(3)・・・・・
・C装置:情報処理装置、(4)・・・・・・D゛イン
ターフエースカードである。
J特許庄斡人 −剖准制御珠入な゛社
代理人 弁理士 佐 藤 英 昭
實Sol : J5./ (ZJ
tsO2: 9B、E (%)**オ*ボlI
幕 0\’YGE/υ10υILrBR丁IJMcυR
VE γオAロオ↓1* Sf:tgrdard a
−v (X)2 : 、S’+2.4! Manual
すb 酌Figure 1 is an explanatory diagram of the hemoglobin oxygen equilibrium curve OEC;
FIG. 2 is a block diagram of a device showing an embodiment of the present invention, FIG. 3 is a block diagram of internal functions of an information processing device used in this embodiment, and FIG. 4 is a block diagram of a C RT according to this embodiment.
An example of the oxygen balance curve and data table printed on the display and notebook copy, FIG.
! FIG. In the figure, [11...A device: blood gas analysis device, (2)--
...B device: CO oximeter, (3)...
- C device: information processing device, (4)... D゛interface card. J Patent Shojin - Autopsy Associate Control Involved Company Agent Patent Attorney Hide Sato Akiyoshi Sol: J5. / (ZJ
tsO2: 9B,E (%)**O*Boll
Curtain 0\'YGE/υ10υILrBR ding IJMcυR
VE γoAroo↓1* Sf:tgrdard a
-v (X)2: , S'+2.4! Manual
sb cup
Claims (1)
田バ重炭酸水素イオン(HCOI)、総ヘモグロビン及
び総ヘモグロビン(二含有される諸因子(%02)(b
、%Q)Hb、%MetHb、その曲)等の情報が74
すられる各種の分析装置と、こitらの装置からの出力
を受入れて特別の規定菟二従つ1情報処理装置Δの内部
接続を構成するインターフェースカードと、このインタ
ーフェースカードを受入れで内部接続を完成し所定の情
報処理を自動的(−実施する情報処理装置とを具備し、
小骨の血液を被測定物として導入すること一二よって定
められた標準東注下及び生体内条件下【二おける血液の
酸素運搬能力を解析し、更(−肺や血液)二よって行な
われる各種内呼吸区二関する情報を自動的C二解析し、
CRT上口表示すると共Cニハードコピーとして出力し
、更(二これらのすべてのデータを蓄積し、必要に応じ
て出力する機能を有することを特徴とする内呼枝情報の
自動解析測定装置。 (2)−1ニベ己内呼吸情報の自動11fl析測5]テ
装置をr吏用し、血中酸素酸や、ヘモグロビン等各種の
分析を情報処理装置?t+−導入し、少惜の静脈血を測
定対象として定めら桟だ標準条件下(−よ、−けるヘモ
グロビン(Hb)の酸素運1般11ヒカを示す酸素平衡
曲線と当該曲線上で係02F−(b50係に対応する酵
素分[ト0す、)であろP、。値と当該血液での理論的
02渾1般可能惜を表すSt6.−v I)o2並び−
二生体条「ト丁τ二おける実態α℃とP5oの静脈血の
みで測定を完−rする段階と、この静脈血(二よって得
ら1′1.た各種の分析結毀を前記情報処理装置の記憶
部(二蓄積する段階と、前記静脈血分析と同様の手法(
二よって得らftだ動脈血の分析値全情報処理装置(二
導入し上3[:蓄積さitた静脈血情報との比較及びそ
の相互作用(−よって修飾された標準化OEC,P
St’a−v I)o2と共(−実50’ 態のOEC、P 5(1%史(二生木内の動、静脈血間
で実際(二消費されている酸素鍍を表すa−v I)o
2、肺胞内外で行なわにる02 のガス拡散較差A−a
I)o2肺胞・ぐイ・やス率の指標である5hunt率
等、肺及び血液を通して行なわれる内呼吸(二関する各
種の情報を定められた手法に基づき自動的C−解析し、
与えられた、それぞり、■値と共(=CRT及びハード
コピーとして所定の形で表示する段階と、これらすべて
のデータを蓄積し必要;−6じて表示するデータパンク
の機能を東す段階とを有することを特徴とする内呼吸情
報の自動解析測定方法。[Claims] (11 Blood oxygen meter, carbon dioxide needle, hydrogen ion concentration (
Tabata bicarbonate ion (HCOI), total hemoglobin and total hemoglobin (2) contained factors (%02) (b
, %Q)Hb, %MetHb, the song) etc. is 74
The various analytical devices that are used, and the interface card that accepts the output from these devices and configures the internal connections of the information processing device Δ, and the interface card that accepts the output from these devices and configures the internal connections. Completed and equipped with an information processing device that automatically carries out predetermined information processing,
Introducing the blood in the ossicles as the object to be measured (1) Analyzing the oxygen carrying capacity of the blood under standard conditions and in vivo conditions (2) (-lungs and blood) Automatically analyzes information related to the internal breathing area,
An apparatus for automatically analyzing and measuring internal call branch information, characterized in that it has a function of displaying on a CRT, outputting it as a hard copy, accumulating all of these data, and outputting it as necessary. (2)-1 Automatic 11fl analysis of internal respiration information 5] We used an information processing device to perform various analyzes such as blood oxygen and acid, hemoglobin, etc. The oxygen balance curve that shows the oxygen transport of hemoglobin (Hb) under standard conditions (-1), which is determined when blood is the measurement target, and the enzyme fraction corresponding to the 02F-(b50) [To0su,) is P, .St6.-v I) o2 arrangement- which represents the theoretical 02 1 general possibility of the value and the blood concerned.
The second step is to complete the measurement using only venous blood of α℃ and P5o, and perform various analysis results obtained from this venous blood (1'1) through the information processing described above. The storage part of the device (two accumulation stages and the same method as the venous blood analysis described above)
2. Therefore, the analytical values of arterial blood obtained by the total information processing device (2) are introduced, and 3.
St'a-v I) together with o2 (-actual 50' state of OEC, P5 (1% history (a-v representing the actual (2) consumed oxygen between the arterial and venous blood in the two living trees) I)o
2. 02 gas diffusion difference A-a that takes place inside and outside the alveoli
I) Internal respiration performed through the lungs and blood, such as the 5hunt rate, which is an index of the o2 alveolar, gui, and gas rate (2) Automatic C-analysis of various information related to
Given, respectively, the stage of displaying (=displaying in a predetermined form as CRT and hard copy) and the need to store and display all these data; 1. A method for automatic analysis and measurement of internal respiration information, comprising steps.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP58005791A JPS59145967A (en) | 1983-01-19 | 1983-01-19 | Method and device for measuring information on internal respiration by automatic analysis |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP58005791A JPS59145967A (en) | 1983-01-19 | 1983-01-19 | Method and device for measuring information on internal respiration by automatic analysis |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS59145967A true JPS59145967A (en) | 1984-08-21 |
JPH0364124B2 JPH0364124B2 (en) | 1991-10-04 |
Family
ID=11620906
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP58005791A Granted JPS59145967A (en) | 1983-01-19 | 1983-01-19 | Method and device for measuring information on internal respiration by automatic analysis |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS59145967A (en) |
-
1983
- 1983-01-19 JP JP58005791A patent/JPS59145967A/en active Granted
Also Published As
Publication number | Publication date |
---|---|
JPH0364124B2 (en) | 1991-10-04 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
Boix-Ochoa et al. | Acid-base balance and blood gases in prognosis and therapy of congenital diaphragmatic hernia | |
Cole et al. | Effect of varying inspired O2 tension on alveolar-arterial O2 tension difference in man | |
EP0449971A4 (en) | Methods and apparatus for cardiac output measurement | |
US20130109978A1 (en) | Non-invasive cardiac output determination | |
WO2020052433A1 (en) | Adequacy assessment method and system | |
JP4541887B2 (en) | Method, system and device for converting venous blood values to arterial blood values | |
Israel et al. | Fatal hemoptysis from pulmonary arteriovenous fistula | |
JPS59145967A (en) | Method and device for measuring information on internal respiration by automatic analysis | |
ES2982313T3 (en) | An improved procedure for estimating arterial blood values | |
US7662632B2 (en) | Method for performing a non-invasive blood gas test | |
Willis et al. | Additional blood-gas variables for the rational control of oxygen therapy: with allowance for shifts of the oxygen dissociation curve | |
Berry et al. | Assessing tissue oxygenation | |
Hope et al. | Non-invasive estimation of venous admixture: validation of a new formula | |
JP2006122111A (en) | Oxygenator gas exchange monitor | |
Rosner et al. | A computer program for computation and interpretation of pulmonary function data | |
Waddell et al. | The practitioner’s acid-base primer: obtaining & interpreting blood gases | |
Kost et al. | Indications for measurement of total carbon dioxide in arterial blood. | |
Douglas et al. | A comparison of methods for the measurement of cardiac output and blood oxygen content | |
Karis et al. | Clinical evaluation of the Edwards Laboratories and Oximetrix mixed venous oxygen saturation catheters | |
Nunn | The lung as a black box | |
Canizaro et al. | A technique for estimating the position of the oxygen-hemoglobin dissociation curve | |
Hazarika et al. | Does Arterial Blood Gas (ABG) Provide a Safety Net for Extubation in Surgical Patients? | |
Perak et al. | Noninvasive cardiac output estimation by inert gas rebreathing in mechanically ventilated pediatric patients | |
Woda et al. | Effect of measurement error on calculated variables of oxygen transport | |
EP0234826A2 (en) | Method and apparatus for measuring novel blood gas parameters |