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JPS6216647B2 - - Google Patents
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JPS6216647B2 - - Google Patents

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Publication number
JPS6216647B2
JPS6216647B2 JP54029573A JP2957379A JPS6216647B2 JP S6216647 B2 JPS6216647 B2 JP S6216647B2 JP 54029573 A JP54029573 A JP 54029573A JP 2957379 A JP2957379 A JP 2957379A JP S6216647 B2 JPS6216647 B2 JP S6216647B2
Authority
JP
Japan
Prior art keywords
absorbance
light
signal
calculating
hbp2
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.)
Expired
Application number
JP54029573A
Other languages
Japanese (ja)
Other versions
JPS55120858A (en
Inventor
Kenji Hamaguri
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.)
Minolta Co Ltd
Original Assignee
Minolta 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 Minolta Co Ltd filed Critical Minolta Co Ltd
Priority to JP2957379A priority Critical patent/JPS55120858A/en
Publication of JPS55120858A publication Critical patent/JPS55120858A/en
Publication of JPS6216647B2 publication Critical patent/JPS6216647B2/ja
Granted legal-status Critical Current

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  • Investigating Or Analysing Biological Materials (AREA)
  • Measurement Of The Respiration, Hearing Ability, Form, And Blood Characteristics Of Living Organisms (AREA)

Description

【発明の詳細な説明】[Detailed description of the invention]

本発明は、生体の動脈血のO2飽和度の絶対値
を非観血的に測定するオキシメーターに関し、さ
らに詳しくはHb(ヘモグロビン)とHbO2(酸化
ヘモグロビン)の光吸収特性が異ることを利用
し、生体中において吸収を受けた光を分折するこ
とにより上記測定を行う非観血オキシメーターに
関する。 従来、血液を生体から採取せずに非観血的に酸
素飽和度を測定するオキシメータとして、血液の
脈動による吸光度の変化分を利用するものが知ら
れている。この装置は、吸光度の変化分から情報
を得ているので、測定出力の定常成分すなわち、
生体の組織等による吸光度の影響を受けることが
なく、この影響を除くために従来必要とされた被
測定部の虚血という操作が不要であり、その結果
酸素飽和度を連続的に測定できるという長所を持
つている。しかしながら、この装置は測定出力の
変化変分を情報源としているため被測定部が動揺
するとその影響が測定信号の変化成分として現わ
れ、これが測定値に誤差として混入するという欠
点があつた。 本発明は上記欠点を改善することを目的とする
ものであり、被測定部が動揺しても高精度で測定
が可能な非観血オキシメータを提供するものであ
る。 以下図示の実施例に基いて、本発明を説明す
る。第1図は、本発明の実施例を示すブロツク図
である。第1図において、被測定部2を透過した
光はダイクロイツクミラー3、ダイクロイツクミ
ラー4、および干渉フイルター5、干渉フイルタ
ー6、干渉フイルター7により3つの波長域に分
割され、受光部8、受光部9、受光部10にそれ
ぞれ入射する。受光部8、受光部9、受光部10
の出力Ea1、Ea2、Ea3はそれぞれ Ea1=IO1(1+α)F110−C{S( 1εHbp21εHb)+ 1εHb}(d+△d) ―(1) Ea2=IO2(1+α)F210−C{S( 2εHbp22εHb)+ 2εHb}(d+△d) ―(2) Ea3=IO3(1+α)F310−C{S( 3εHbp23εHb)+ 3εHb}(d+△d) ―(3) と表わされる。Ip1、Ip2、Ip3はそれぞれ第
1、第2および第3の波長域の入射光強度、F
1、F2、F3はそれぞれ第1、第2、第3の波長
域の光に対する動脈血以外の組織の透過率、 1ε
Hbp22εHbp23εHbp2はそれぞれ第1、第2、
第3の波長域の光に対する酸化ヘモグロビンの吸
光係数、 1εHb2εHb3εHbはそれぞれ第
1、第2、第3の波長域の光に対するヘモグロビ
ンの吸光係数、Cは総ヘモグロビン濃度、dは組
織内にプールされた血液の厚さで△dはその、脈
動による変化分、Sは動脈血の酸素飽和度、αは
被測定部の動揺による入射光強度の変化率であ
る。式(1),(2),(3)から解る様に受光部の出力はそ
れぞれ直流成分と交流成分を含んでいる。11,
12,13はそれぞれ受光部8,9,10の出力
からそれぞれ吸光度の変化分を計算する演算回路
である。吸光度の変化分は例えば、それぞれの受
光部の出力の直流成分に対する交流成分の比を演
算回路11,12,13で求めることによつて得
られる。すなわち式(1),(2),(3)を書き直すと、 Eai〓Ipi(1+α)Fi10−C{S( iεHbp2iεHb)+ iεHb}d X〔1−ln10・C{S( iεHbp2iεHb)+ iεHb}△d〕 〓IOiFi10−C{S( iεHbp2iεHb)+ iεHb}d X〔1+α−ln10・C{S( iεHbp2iεHb)+ iεHb}△d〕 ―(4) ただし、上記においてi=1,2,3で、式
(1),(2),(3)の三つの場合が式(4)で同時に表わされ
ている。従つて演算回路11,12,13でそれ
ぞれEaiの直流成分に対するEaiの交流成分の比
の演算を行い以下の出力Ebi(i=1,2,3)
を得る。 Ebi=α−ln10・C{S( iεHbp2iεHb)+ iεHb}△d ―(5) (5)式から明らかなように、演算回路11,12,
13の出力は受光部8,9,10への入射光強度
へ変化分のみの情報となつている。しかしながら
被測定部の動揺によるフアクターであるαもまた
入射光強度の変化分であるので出力Ebi中に含ま
れている。従来は、2波長についてEb1,Eb2
得、この2つの出力からSを求めていたが、上記
αの影響を消去することができず、それが測定誤
差の原因となつていた。 そこで、本発明では3波長について得たEb1
Eb2,Eb3を差動増巾器14,15に入力し、そ
れぞれ(Eb1−Eb3)及び(Eb2−Eb3)の演算を行
わせている。すなわち、差動増巾器14,15の
出力Ec1,Ec2はそれぞれ、 Ec1=ln10・C・△d〔S{( 1εHbp23εHbp2) −( 1εHb3εHb)}+( 1εHb3εHb)〕 ―(6) Ec2=ln10・C・△d〔S{( 2εHbp23εHbp
) −( 2εHb3εHb)}+( 2εHb3εHb)〕 ―(7) となる。式(6)(7)よりSを求めると、
The present invention relates to an oximeter that non-invasively measures the absolute value of O 2 saturation in arterial blood of a living body, and more specifically, the present invention relates to an oximeter that non-invasively measures the absolute value of O 2 saturation in arterial blood of a living body. The present invention relates to a non-invasive oximeter that performs the above measurements by diffracting the light absorbed in the living body. BACKGROUND ART Conventionally, as an oximeter that measures oxygen saturation non-invasively without collecting blood from a living body, one that utilizes changes in absorbance due to blood pulsation is known. This device obtains information from changes in absorbance, so the steady component of the measurement output, that is,
It is not affected by the absorbance of living body tissues, and there is no need to perform ischemia of the measurement area, which was previously required to remove this effect, and as a result, oxygen saturation can be measured continuously. Has advantages. However, since this device uses variations in the measurement output as its information source, when the part to be measured moves, the effect appears as a variation component in the measurement signal, which has the disadvantage of being mixed into the measurement value as an error. The present invention aims to improve the above-mentioned drawbacks, and provides a non-invasive oximeter that can perform measurements with high accuracy even when the part to be measured is shaken. The present invention will be explained below based on the illustrated embodiments. FIG. 1 is a block diagram showing an embodiment of the present invention. In FIG. 1, the light transmitted through the part to be measured 2 is divided into three wavelength ranges by a dichroic mirror 3, a dichroic mirror 4, an interference filter 5, an interference filter 6, and an interference filter 7. The light enters the light receiving section 9 and the light receiving section 10, respectively. Light receiving section 8, light receiving section 9, light receiving section 10
The outputs E a1 , E a2 , and E a3 are respectively E a1 =I O1 (1+α)F 1 10−C{S( 1 ε Hbp21 ε Hb ) +1 ε Hb }(d+△d) −(1) E a2 =I O2 (1+α)F 2 10−C{S( 2 ε Hbp22 ε Hb )+ 2 ε Hb }(d+△d) ―(2) E a3 = I O3 (1+α) F 3 10− It is expressed as C{S( 3 ε Hbp23 ε Hb ) +3 ε Hb }(d+△d) - (3). I p1 , I p2 , and I p3 are the incident light intensities in the first, second, and third wavelength ranges, respectively, and F
1 , F 2 , and F 3 are the transmittance of tissues other than arterial blood to light in the first, second, and third wavelength ranges, respectively, and 1 ε
Hbp2 , 2 ε Hbp2 , 3 ε Hbp2 are the first, second, and
The extinction coefficient of oxyhemoglobin for light in the third wavelength range, 1 ε Hb , 2 ε Hb , 3 ε Hb is the extinction coefficient of hemoglobin for light in the first, second, and third wavelength range, respectively, and C is the total hemoglobin. The concentration, d, is the thickness of blood pooled in the tissue, Δd is the variation thereof due to pulsation, S is the oxygen saturation level of arterial blood, and α is the rate of change in the intensity of the incident light due to agitation of the part to be measured. As can be seen from equations (1), (2), and (3), the output of the light receiving section includes a DC component and an AC component, respectively. 11,
12 and 13 are arithmetic circuits that calculate changes in absorbance from the outputs of the light receiving sections 8, 9, and 10, respectively. The change in absorbance can be obtained, for example, by calculating the ratio of the AC component to the DC component of the output of each light receiving section using the calculation circuits 11, 12, and 13. That is, if we rewrite equations (1), (2), and (3), E ai 〓I pi (1+α)F i10 −C{S( i ε Hbp2i ε Hb )+ i ε Hb }d X[1− ln10・C{S( i ε Hbp2i ε Hb )+ i ε Hb }△d} 〓I Oi Fi10−C{S( i ε Hbp2i ε Hb )+ i ε Hb }d X[1+α−ln10・C{S( i ε Hbp2i ε Hb )+ i ε Hb }△d] - (4) However, in the above, when i = 1, 2, 3, the formula
Three cases (1), (2), and (3) are expressed simultaneously in equation (4). Therefore, the calculation circuits 11, 12, and 13 each calculate the ratio of the AC component of E ai to the DC component of E ai , and the following output E bi (i=1, 2, 3) is obtained.
get. E bi =α−ln10・C{S( i ε Hbp2i ε Hb )+ i ε Hb }△d −(5) As is clear from equation (5), the arithmetic circuits 11, 12,
The output of 13 is information only about changes in the intensity of light incident on the light receiving sections 8, 9, and 10. However, α, which is a factor due to the movement of the measured part, is also included in the output E bi because it is a change in the intensity of the incident light. Conventionally, E b1 and E b2 were obtained for two wavelengths, and S was determined from these two outputs, but the influence of α could not be eliminated, which caused measurement errors. Therefore, in the present invention, Eb 1 ,
Eb 2 and Eb 3 are input to differential amplifiers 14 and 15 to calculate (Eb 1 −Eb 3 ) and (Eb 2 −Eb 3 ), respectively. That is, the outputs Ec 1 and Ec 2 of the differential amplifiers 14 and 15 are respectively E c1 =ln10・C・△d[S{( 1 ε Hbp23 ε Hbp2 ) −( 1 ε Hb3 ε Hb )}+( 1 ε Hb3 ε Hb )] ―(6) E c2 = ln10・C・△d[S{( 2 ε Hbp23 ε Hbp
2 ) −( 2 ε Hb3 ε Hb )}+( 2 ε Hb3 ε Hb )] −(7). Determining S from equations (6) and (7), we get

【表】 第1図における16は、既知の定数 1εHb2
εHb3εHb1εHbp22εHbp23εHbp2と入
力Ec1,Ec2によつて式(8)に従つた演算を行う酸
素飽和度演算部である。その出力は表示部17に
よつて表示される。式(6),(7)から明らかなように
αの影響はSの演算に混入していない。 以上から明らかなように、本発明によれば、被
測定部の動揺にかかわらず連続して正確な測定の
可能な非観血オキシメータが提供される。
[Table] 16 in Figure 1 is the known constant 1 ε Hb , 2
This is an oxygen saturation calculation unit that performs calculation according to equation (8) using ε Hb , 3 ε Hb , 1 ε Hbp2 , 2 ε Hbp2 , 3 ε Hbp2 and inputs Ec 1 and Ec 2 . The output is displayed on the display section 17. As is clear from equations (6) and (7), the influence of α is not mixed into the calculation of S. As is clear from the above, according to the present invention, a non-invasive oximeter is provided that is capable of continuous and accurate measurement regardless of the movement of the part to be measured.

【図面の簡単な説明】[Brief explanation of the drawing]

図面は、本発明の一実施例を示すブロツク図で
ある。 8,9,10……受光部、11,12,13…
…演算回路、14,15……差動増巾器、16…
…酸素飽和度演算部。
The drawing is a block diagram showing one embodiment of the present invention. 8, 9, 10... light receiving section, 11, 12, 13...
...Arithmetic circuit, 14, 15...Differential amplifier, 16...
...Oxygen saturation calculation section.

Claims (1)

【特許請求の範囲】 1 脈動する血液を含む生体によつて吸収を受け
た3種の波長の光量をそれぞれ検出し、光量に応
じた出力信号を発生する第1,第2,第3の受光
手段と、 この3つの受光手段の出力信号のそれぞれにつ
いて血液の脈動による吸光度の変化分を計算し、
それに応じた第1,第2,第3の吸光度信号をそ
れぞれ出力する第1,第2,第3の演算手段と、 第1の吸光度信号と第3の吸光度信号との差を
計算しそれに応じた第1の差動信号を出力する第
1の差動手段と、 第2の吸光度信号と第3の吸光度信号との差を
計算しそれに応じた第2の差動信号を出力する第
2の差動手段と、 第1及び第2の差動信号に基づいて血液の酸素
飽和度を演算する酸素飽和度演算手段と を有することを特徴とする非観血オキシメー
タ。
[Scope of Claims] 1. First, second, and third light receivers that detect the amount of light of three different wavelengths absorbed by a living body including pulsating blood, and generate an output signal according to the amount of light. and calculating the change in absorbance due to blood pulsation for each of the output signals of the three light receiving means,
first, second, and third calculating means that respectively output first, second, and third absorbance signals corresponding to the calculation means; and calculating a difference between the first absorbance signal and the third absorbance signal and responding accordingly. and a second differential means that calculates a difference between the second absorbance signal and the third absorbance signal and outputs a second differential signal corresponding to the difference between the second absorbance signal and the third absorbance signal. A non-invasive oximeter comprising: differential means; and oxygen saturation calculating means for calculating the oxygen saturation of blood based on the first and second differential signals.
JP2957379A 1979-03-13 1979-03-13 Nonnvisual oxyymeter Granted JPS55120858A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP2957379A JPS55120858A (en) 1979-03-13 1979-03-13 Nonnvisual oxyymeter

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP2957379A JPS55120858A (en) 1979-03-13 1979-03-13 Nonnvisual oxyymeter

Publications (2)

Publication Number Publication Date
JPS55120858A JPS55120858A (en) 1980-09-17
JPS6216647B2 true JPS6216647B2 (en) 1987-04-14

Family

ID=12279848

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2957379A Granted JPS55120858A (en) 1979-03-13 1979-03-13 Nonnvisual oxyymeter

Country Status (1)

Country Link
JP (1) JPS55120858A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH01317853A (en) * 1988-06-20 1989-12-22 Masao Mangyo Commodity storage utilizing lower part space of vehicle

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2015039542A (en) 2013-08-22 2015-03-02 セイコーエプソン株式会社 Pulse wave measuring device
JP6519978B2 (en) 2014-03-27 2019-05-29 セイコーエプソン株式会社 Biological information detection apparatus and electronic device
JP5929952B2 (en) 2014-03-27 2016-06-08 セイコーエプソン株式会社 Biological information detection apparatus and electronic device
EP3355775B1 (en) * 2015-09-28 2019-05-22 Koninklijke Philips N.V. Vital signs sensor and method of measuring vital signs of a user

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5725217B2 (en) * 1974-10-14 1982-05-28
US4167331A (en) * 1976-12-20 1979-09-11 Hewlett-Packard Company Multi-wavelength incremental absorbence oximeter

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH01317853A (en) * 1988-06-20 1989-12-22 Masao Mangyo Commodity storage utilizing lower part space of vehicle

Also Published As

Publication number Publication date
JPS55120858A (en) 1980-09-17

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