JPS6410219B2 - - Google Patents
Info
- Publication number
- JPS6410219B2 JPS6410219B2 JP57215916A JP21591682A JPS6410219B2 JP S6410219 B2 JPS6410219 B2 JP S6410219B2 JP 57215916 A JP57215916 A JP 57215916A JP 21591682 A JP21591682 A JP 21591682A JP S6410219 B2 JPS6410219 B2 JP S6410219B2
- Authority
- JP
- Japan
- Prior art keywords
- ray
- blood vessel
- diameter
- film
- reference scale
- 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
Links
- 210000004204 blood vessel Anatomy 0.000 claims description 43
- 238000010521 absorption reaction Methods 0.000 claims description 13
- 239000002872 contrast media Substances 0.000 claims description 11
- 230000002792 vascular Effects 0.000 claims description 10
- 238000003384 imaging method Methods 0.000 claims description 9
- 239000002504 physiological saline solution Substances 0.000 claims description 8
- 238000002583 angiography Methods 0.000 claims description 5
- 239000008280 blood Substances 0.000 claims description 5
- 210000004369 blood Anatomy 0.000 claims description 5
- 238000011160 research Methods 0.000 claims description 4
- 239000000463 material Substances 0.000 claims description 3
- 238000007789 sealing Methods 0.000 claims 1
- 238000000034 method Methods 0.000 description 10
- 238000005259 measurement Methods 0.000 description 9
- 238000010586 diagram Methods 0.000 description 6
- 239000003795 chemical substances by application Substances 0.000 description 4
- 239000004925 Acrylic resin Substances 0.000 description 3
- 229920000178 Acrylic resin Polymers 0.000 description 3
- ADZWSOLPGZMUMY-UHFFFAOYSA-M silver bromide Chemical compound [Ag]Br ADZWSOLPGZMUMY-UHFFFAOYSA-M 0.000 description 3
- 241001465754 Metazoa Species 0.000 description 2
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 2
- 230000005540 biological transmission Effects 0.000 description 2
- 238000011161 development Methods 0.000 description 2
- 239000000839 emulsion Substances 0.000 description 2
- 238000000691 measurement method Methods 0.000 description 2
- 210000000056 organ Anatomy 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- 230000008569 process Effects 0.000 description 2
- 238000012545 processing Methods 0.000 description 2
- 229910052709 silver Inorganic materials 0.000 description 2
- 239000004332 silver Substances 0.000 description 2
- XZNXVSDNACTASG-RZNNTOFGSA-M sodium;3,5-diacetamido-2,4,6-triiodobenzoate;3,5-diacetamido-2,4,6-triiodobenzoic acid;(2r,3r,4r,5s)-6-(methylamino)hexane-1,2,3,4,5-pentol Chemical compound [Na+].CNC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO.CC(=O)NC1=C(I)C(NC(C)=O)=C(I)C(C(O)=O)=C1I.CC(=O)NC1=C(I)C(NC(C)=O)=C(I)C(C([O-])=O)=C1I XZNXVSDNACTASG-RZNNTOFGSA-M 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 230000000007 visual effect Effects 0.000 description 2
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 1
- 208000031872 Body Remains Diseases 0.000 description 1
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- 239000002473 artificial blood Substances 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 238000004141 dimensional analysis Methods 0.000 description 1
- 201000010099 disease Diseases 0.000 description 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 229910052740 iodine Inorganic materials 0.000 description 1
- 239000011630 iodine Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 230000004060 metabolic process Effects 0.000 description 1
- 239000013081 microcrystal Substances 0.000 description 1
- 238000001000 micrograph Methods 0.000 description 1
- 210000004088 microvessel Anatomy 0.000 description 1
- 230000035790 physiological processes and functions Effects 0.000 description 1
- 230000003449 preventive effect Effects 0.000 description 1
- 230000005180 public health Effects 0.000 description 1
- 238000011002 quantification Methods 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- 210000001635 urinary tract Anatomy 0.000 description 1
- 238000011179 visual inspection Methods 0.000 description 1
Landscapes
- Measurement Of The Respiration, Hearing Ability, Form, And Blood Characteristics Of Living Organisms (AREA)
- Apparatus For Radiation Diagnosis (AREA)
Description
【発明の詳細な説明】
本発明は、血管のX線写真画像における血管像
の解析の定量化を図るため、血管径のX線造影時
に使用する簡便な基準スケールに関するものであ
る。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a simple reference scale used during X-ray imaging of blood vessel diameters in order to quantify the analysis of blood vessel images in X-ray images of blood vessels.
レントゲンによつて発明されたX線は、非観血
かつ無侵襲で生体内部の観測ができ、医学分野で
幅広く利用されており、可視光線と同じ作用を写
真フイルムにおよぼす。X線写真フイルムは感光
乳剤層とベースからできており、これにX線が照
射されると感光乳剤層中に含まれている臭化銀の
微結晶が変化を受け、潜像を形成する。X線照射
後のフイルムを現像すると、X線の作用を受けた
臭化銀が還元されて銀粒子となる。X線の作用を
受けない臭化銀はそのまま残り、定着により溶解
してフイルム上から取り除かれ透明となる。また
還元された銀粒子はフイルム上に残存し黒くな
る。X線が被写体を透過する際の被写体のX線の
吸収係数の大小により、X線写真フイルム上に濃
淡像が形成される。 X-rays, invented by Roentgen, can observe the inside of a living body non-invasively and are widely used in the medical field, and have the same effect on photographic film as visible light. An X-ray photographic film is made up of a light-sensitive emulsion layer and a base, and when the film is irradiated with X-rays, the silver bromide microcrystals contained in the light-sensitive emulsion layer undergo a change, forming a latent image. When the film after X-ray irradiation is developed, the silver bromide that has been affected by the X-rays is reduced to become silver particles. Silver bromide, which is not affected by the X-rays, remains as it is and is dissolved during fixing and removed from the film, making it transparent. Further, the reduced silver particles remain on the film and turn black. A grayscale image is formed on the X-ray photographic film depending on the magnitude of the X-ray absorption coefficient of the subject when the X-rays pass through the subject.
生体が自然の状態のままでX線写真の十分な濃
淡像が得られるのは、測定対象器管のX線吸収係
数が周囲の組織のX線吸収係数と大きく異なる場
合だけで、生体の大部分は目的対象と周囲の組織
の間のX線吸収係数の差は極めて小さい。鮮明な
X線画像を得るためには、周囲の組織に比較して
X線をよく吸収するか、または逆によく透過する
物質を測定対象器管内に注入する必要がある。血
管系の造影剤としては、X線の吸収係数の大き
い、有機ヨード系造影剤が最もよく使用されてい
る。 Sufficient density images can be obtained in an X-ray photograph when the body remains in its natural state only when the X-ray absorption coefficient of the organ to be measured differs significantly from that of the surrounding tissue. The difference in X-ray absorption coefficient between the target object and the surrounding tissue is extremely small. In order to obtain clear X-ray images, it is necessary to inject into the organ to be measured a substance that absorbs or transmits X-rays better than the surrounding tissue. As contrast agents for the vascular system, organic iodinated contrast agents, which have a large X-ray absorption coefficient, are most often used.
生体の代謝に必要な各種物質を血液に託して、
体の一部から他の一部へ輸送するパイプとしての
血管造影時の観測は、循環器系疾患の診断及び血
管循環器系の生理学的機能の解明のため、極めて
重要である。血管の次元解析において重要な要素
である血管径をX線写真画像から読取ることは、
医師の目視判断によるところが大である。予防医
学及び国民の健康管理の認識の高まりにより、処
理すべき血管像の画像の量は飛躍的に増加してい
る。一方、医師及び熟練検査技師の不足はいちじ
るしくなつており、従来の目視主体の処理を定量
的に自動化する社会的要請は極めて大である。 Entrusting various substances necessary for the metabolism of the living body to the blood,
Observation during angiography as a conduit for transporting blood from one part of the body to another is extremely important for diagnosing circulatory system diseases and elucidating the physiological functions of the vascular circulatory system. Reading the blood vessel diameter from X-ray images, which is an important element in dimensional analysis of blood vessels, is
Much depends on the visual judgment of the doctor. With increasing awareness of preventive medicine and public health management, the amount of vascular images to be processed is increasing dramatically. On the other hand, there is a serious shortage of doctors and skilled laboratory technicians, and there is an extremely strong social need to quantitatively automate the conventional visual inspection-based processing.
従来、X線画像から血管径を定量化するために
は以下のような方法が存在していた。 Conventionally, the following methods have been used to quantify blood vessel diameter from X-ray images.
(1) X線写真フイルムの画像をスライドプロジエ
クタでスクリーン上に拡大するか、あるいは、
写真引伸機を用いて拡大して印画紙上に焼きつ
けて、これらの拡大された血管像から観測者が
ものさしを用いて、血管径を計測する方法。(1) Enlarge the image of the X-ray photographic film on a screen with a slide projector, or
A method in which blood vessels are enlarged using a photo enlarger and printed onto photographic paper, and an observer uses a ruler to measure the diameter of blood vessels from these enlarged images.
(2) X線写真フイルムの画像を顕微鏡で拡大して
観測者が目視で測定するか、あるいは、顕微鏡
画像をテレビカメラで撮影し、この出力映像信
号を2値化して、その幅から血管径を測定する
方法。(2) The X-ray photographic film image can be enlarged with a microscope and measured visually by an observer, or the microscope image can be photographed with a television camera, the output video signal can be binarized, and the blood vessel diameter can be determined from the width. How to measure.
前記(1)の方法では、X線写真フイルム画像をレ
ンズで拡大するため、ボケが生じ血管とバツクグ
ラウンド及び血管壁の境界がはつきりしなくな
り、測定誤差が生じるとともに、血管径の微細な
変化を検出することが極めて困難である。また、
測定はもつぱら人力によるため、測定者の個人的
な測定精度のバラツキが生じ、処理できる点数及
び画像枚数に限度があり、多量のX線写真フイル
ムを処理することは極めて困難である。 In method (1) above, since the X-ray film image is magnified with a lens, blurring occurs and the boundaries between the blood vessel, the background, and the blood vessel wall become blurred, resulting in measurement errors and the possibility of minute differences in the diameter of the blood vessel. Changes are extremely difficult to detect. Also,
Since the measurement is performed solely by human labor, there are variations in measurement accuracy among the individual measurers, and there is a limit to the number of points and images that can be processed, making it extremely difficult to process a large amount of X-ray photographic film.
(2)の方法は主に微小血管径の計測に用いられて
おり、顕微鏡で画像を拡大すると、(1)の方法に比
較すると測定精度は向上するが、1回の測定で処
理できる点数は1点であるため、1つの画像から
何点もの点を計測する場合は、計測するのに多大
の労力と時間を要し、多量の画像の定量化が望ま
れている社会的要請に答えることは極めて困難で
ある。 Method (2) is mainly used to measure the diameter of microvessels, and when the image is enlarged with a microscope, the measurement accuracy improves compared to method (1), but the number of points that can be processed in one measurement is Since it is a single point, it takes a lot of effort and time to measure many points from one image, and this is to meet the social demand for quantification of a large number of images. is extremely difficult.
以上のように、従来の血管径の計測法では、X
線画像中に基準となるものが撮影されていなく、
計測はもつぱら目視判断によつているため、多量
のX線写真画像の処理及びその定量化を行うに当
り、高速、正確、経済性にみあう方法がなかつ
た。 As mentioned above, in the conventional measurement method of blood vessel diameter,
The reference object is not captured in the line image,
Since measurements are based solely on visual judgment, there has been no fast, accurate, and economical method for processing and quantifying a large number of X-ray photographic images.
本発明者らは、こうした現状に鑑み、X線写真
フイルム画像から血管径の定量化について鋭意検
討を行つた結果、本発明をなすに致つた。すなわ
ち、本発明は、血管系X線写真画像から血管径を
定量化するため、血管系のX線造影時に測定対象
被写体と同時、あるいは同一条件で撮影すること
を特徴とする簡易な基準スケールに関するもので
ある。 In view of the current situation, the present inventors have conducted intensive studies on quantifying blood vessel diameters from X-ray photographic film images, and as a result, have completed the present invention. That is, the present invention relates to a simple reference scale that is characterized in that it is imaged at the same time as the object to be measured or under the same conditions during X-ray imaging of the vascular system in order to quantify the diameter of a blood vessel from an X-ray image of the vascular system. It is something.
このため、人体及び実験研究用生体とX線吸収
係数が等価な材質内に、X線造影対象の血管に対
応するそれぞれ異なる径で、かつ各径が既知の数
種類の細長い断面が円形状の穴をあけ、この数種
類の各穴内(または各穴内に挿入された血管に相
当するパイプ内)に生理食塩水及び血管造影時に
使用する場合と等濃度の血管造影剤を注入し、こ
の両端を密封することを特徴とする。 For this reason, several kinds of elongated holes with circular cross sections, each with a different diameter and each diameter known, are made in a material whose X-ray absorption coefficient is equivalent to that of the human body or a living body for experimental research. , inject physiological saline and an angiographic contrast agent at the same concentration as that used during angiography into each of these several types of holes (or into the pipe corresponding to the blood vessel inserted into each hole), and seal both ends. It is characterized by
以下、本発明の実施例として、実験研究用動物
の血管系のX線造影時に用いる基準スケールの場
合について詳述する。 Hereinafter, as an example of the present invention, a reference scale used for X-ray imaging of the vascular system of an experimental research animal will be described in detail.
第1図は、本発明の基準スケールの概要を示す
ものであり、第2図a,bはその正面図及び側面
図である。基準スケール本体1は、X線の吸収係
数が生体に近いアクリル樹脂を使用し、その厚さ
は7mmとした。観測対象となる血管径は0.5〜2
mmの範囲内であるがため、基準スケール本体1に
第1図に示すように、径が0.58〜1.67mmまでの5
種類モデル血管に相当する穴2をドリルを用いて
あける。穴の径の仕上り寸法は顕微鏡あるいは拡
大プロジユクで正確な値を測定する。基準スケー
ル本体1の厚さは、実験研究用動物の測定対象部
分のX線吸収係数と等価となるように厚さを調節
する。測定部分のX線吸収係数が大きく、厚さだ
けで調節が困難な場合は、アルミニユウムなどの
フイルタ3を用いて吸収率の調節を行う。 FIG. 1 shows an outline of the reference scale of the present invention, and FIGS. 2a and 2b are a front view and a side view thereof. The reference scale main body 1 was made of acrylic resin with an X-ray absorption coefficient close to that of a living body, and its thickness was 7 mm. The diameter of the blood vessel to be observed is 0.5 to 2.
Since the diameter is within the range of 0.58 to 1.67 mm, the reference scale main body 1 is equipped with 5 mm diameters, as shown in Figure 1.
A hole 2 corresponding to the type model blood vessel is made using a drill. The finished diameter of the hole is determined accurately using a microscope or a magnification projector. The thickness of the reference scale main body 1 is adjusted so that it becomes equivalent to the X-ray absorption coefficient of the measurement target part of the experimental research animal. If the X-ray absorption coefficient of the measurement part is large and difficult to adjust based on the thickness alone, the absorption coefficient is adjusted using a filter 3 made of aluminum or the like.
次に、モデル血管に相当する基準スケール本体
1の各種の細長い穴の中に血液と等価な生理食塩
水及び造影剤の注入法について説明する。第3図
はそのための装置の概略図である。まず、基準ス
ケール本体1を縦にして容器4に入れ、この容器
4を真空用ベルジユア5に入れ、真空ポンプ6を
用いてベルジユア5内を真空にする。上部に設け
た容器7には、生理的食塩水あるいは血管造影剤
を入れておき、ベルジユア5内が真空になるとコ
ツク8を開き、容器7の造影剤を滴下させ、基準
スケール本体1の中に徐々に造影剤を満たす。基
準スケール本体1の各パイプ中に造影剤が充満し
たら、コツク8を閉じ、真空用ベルジユア5に空
気を入れ、基準スケール本体1を取り出し、パイ
プの両端に設けられたネジ及びパツキンを閉じて
造影剤を密封する。 Next, a method of injecting physiological saline equivalent to blood and a contrast medium into various long and narrow holes of the reference scale main body 1 corresponding to model blood vessels will be explained. FIG. 3 is a schematic diagram of a device for this purpose. First, the reference scale main body 1 is placed vertically into a container 4, this container 4 is placed in a vacuum vergeur 5, and the inside of the vergeur 5 is evacuated using the vacuum pump 6. A container 7 provided at the top is filled with physiological saline or an angiographic contrast agent, and when the inside of the vergeure 5 is vacuumed, the container 8 is opened and the contrast agent in the container 7 is dripped into the reference scale body 1. Gradually fill with contrast medium. When each pipe of the reference scale main body 1 is filled with the contrast medium, close the pot 8, let air into the vacuum vergeure 5, take out the reference scale main body 1, close the screws and gaskets provided at both ends of the pipes, and contrast. Seal the agent.
本発明において、まず造影剤が注入される前段
階のモデル血管用基準スケールとして、基準スケ
ール本体1内に、上記説明による方法で生理的食
塩水のみを注入したものを製作した。次に、血管
用造影として、尿路及び血管造影用の水溶性有機
ヨード剤であるウログラフインを用い、ウログラ
フイン濃度が30%,60%,76%の3種類の基準ス
ケールを作製した。 In the present invention, first, as a reference scale for a model blood vessel before a contrast medium is injected, a model blood vessel reference scale was manufactured in which only physiological saline was injected into the reference scale main body 1 by the method described above. Next, for blood vessel imaging, three types of reference scales were prepared using urografin, a water-soluble organic iodine agent for urinary tract and angiography, with urografin concentrations of 30%, 60%, and 76%.
以上のようにして作製した4種類の血管系造影
用基準スケールのX線写真撮影を行い、スケール
として使用できることを以下に説明する。 The four types of reference scales for vascular system contrast produced as described above were taken with X-ray photographs, and the fact that they can be used as scales will be explained below.
第4図は、X線撮影装置の概略図である。使用
したX線撮影装置で、軟X線撮影装置で、管球9
の管電圧は80kV、管電流は30mAとし、管球9
と被写体である基準スケール1との間の距離は
490mmとし、被写体とフイルムは密着させ、X線
露出時間は0.16秒として撮影した。使用したフイ
ルムは軟X線写真撮影用高感度用フイルムであ
る。X線爆写後フイルムカセツテ10内のフイル
ムをX線用現像液(ソフドール)を用い、現像液
の温度を20℃として5分間現像した。現像、定着
後のフイルムに撮影された基準血管となる血管像
を第5図に示す。 FIG. 4 is a schematic diagram of the X-ray imaging apparatus. With the X-ray imaging device used, with the soft X-ray imaging device, tube 9
The tube voltage is 80kV, the tube current is 30mA, and the tube 9
The distance between the object and the reference scale 1 is
The X-ray exposure time was set to 490mm, the subject and film were in close contact, and the X-ray exposure time was 0.16 seconds. The film used was a high-sensitivity film for soft X-ray photography. After X-ray exposure, the film in the film cassette 10 was developed for 5 minutes using an X-ray developer (Sofdol) at a developer temperature of 20°C. FIG. 5 shows an image of a blood vessel serving as a reference blood vessel taken on a film after development and fixation.
現像定着の過程を経てでき上つたX線写真フイ
ルムにI0の強さの白色光線を照射したときの透過
光の強さをIとすると、写真濃度Dは次式により
定義される。 When the X-ray photographic film produced through the development and fixing process is irradiated with a white light beam of intensity I0 , the intensity of the transmitted light is I, and the photographic density D is defined by the following equation.
D=logI0/I ……(1)
第5図に示されているX線画像におけるモデル
血管の中心部の写真濃度を写真濃度計により測定
した。 D=logI 0 /I (1) The photographic density of the center of the model blood vessel in the X-ray image shown in FIG. 5 was measured using a photographic densitometer.
第6図は、本発明において使用したX線写真フ
イルムの写真濃度DとX線の相対露光量の関係を
示す曲線である。縦軸が写真濃度Dであり、横軸
は相対露光量の対数である。 FIG. 6 is a curve showing the relationship between the photographic density D of the X-ray photographic film used in the present invention and the relative exposure amount of X-rays. The vertical axis is the photographic density D, and the horizontal axis is the logarithm of the relative exposure amount.
写真濃度Dとフイルム上に露光されたX線光量
Eが直線関係にある場合は、写真濃度でもつてX
線撮影された像のX線量を評価することができ
る。 If there is a linear relationship between the photographic density D and the amount of X-ray light exposed on the film, then
The X-ray dose of radiographed images can be evaluated.
第6図からわかるように、写真濃度とX線露光
量は直線関係になつていないから、第6図におけ
る特性曲線からX線露光量を読取つて、X線露光
量でX線画像の評価を行う必要がある。第6図に
おける特性曲線は、フイルムに対してあらかじめ
わかつた露光量を与え、それによつて生じる写真
フイルムの濃度を測定し、対数で目盛られた相対
露光量に対しての写真濃度を示したものである。 As can be seen from Figure 6, photographic density and X-ray exposure do not have a linear relationship, so the X-ray exposure can be read from the characteristic curve in Figure 6 and the X-ray image can be evaluated based on the X-ray exposure. There is a need to do. The characteristic curve in Figure 6 is obtained by applying a known exposure amount to the film, measuring the resulting density of the photographic film, and showing the photographic density against the relative exposure amount scaled logarithmically. It is.
第1図における基準スケールをX線撮影する場
合のX線の透過現象をモデル化すると第7図のよ
うになる。基準スケールにおける血管部分のX線
吸収係数をμ1、その径をxとし、血管周辺の生体
組織に相対するアクリル樹脂のX線吸収係数を
μ2、その厚さをdとし、X線源のX線の強さをI1
とし、写真フイルム上に到達するX線の強さをI3
とする。 When the X-ray transmission phenomenon when the reference scale in FIG. 1 is X-rayed is modeled, the result is as shown in FIG. 7. The X-ray absorption coefficient of the blood vessel on the reference scale is μ 1 , its diameter is x, the X-ray absorption coefficient of the acrylic resin facing the living tissue around the blood vessel is μ 2 , its thickness is d, and the X-ray source is X-ray intensity I 1
The intensity of the X-rays reaching the photographic film is I 3
shall be.
X線源において発生された強さI1のX線が、第
1段階において、モデル血管を通過すると、その
出力X線の強さI2は指数法則に従い次式で与えら
れる。 When the X-rays of intensity I 1 generated in the X-ray source pass through the model blood vessel in the first stage, the intensity I 2 of the output X-rays is given by the following equation according to the power law.
I2=I1e-〓1x ……(2)
モデル血管を透過した強さI2のX線は、さらにア
クリル樹脂を通過するから、フイルム上に到達す
るX線の強さI3は、次のようになる。 I 2 = I 1 e - 〓 1x ...(2) Since the X-rays with intensity I 2 that have passed through the model blood vessel further pass through the acrylic resin, the intensity I 3 of the X-rays that reach the film is It will look like this:
I3=I1(e-〓1x×e-〓2d) ……(3)
(3)式の両辺の対数をとると、
logI3=logI1−μ1xloge−μ2dloge
loge=Kとおけば、
logI3−logI1=Kμ1x−Kμ2d
E=logI3/I1=−Kμ1x−Kμ2d ……(4)
(4)式の左辺はX線の相対露光量の対数である。
(4)式において、右辺第2項は一定の値となり、相
対露光量の対数値を測定すれば、血管径xが求め
られる。 I 3 = I 1 (e - 〓 1x ×e - 〓 2d ) ...(3) Taking the logarithm of both sides of equation (3), we get logI 3 = logI 1 −μ 1 xloge−μ 2 dloge loge=K. Then, logI 3 −logI 1 =Kμ 1 x−Kμ 2 d E=logI 3 /I 1 = −Kμ 1 x−Kμ 2 d ...(4) The left side of equation (4) is the relative exposure amount of X-rays. is the logarithm of
In equation (4), the second term on the right side is a constant value, and the blood vessel diameter x can be found by measuring the logarithm of the relative exposure amount.
血管径xとX線の相対露光量の対数値との関係
をグラフで示すと第8図のようになる。横軸が血
管径Xであり、縦軸がX線の相対露光量の対数で
ある。この図からわかるように、血管径xとX線
の相対露光量の対数Eとの間には比例関係が成り
立ち、(4)式が成立することが示される。すなわ
ち、本発明における基準スケールが血管系のX線
造影時における標準血管として使用できることが
明らかになつた。なお、上記の実施例では穴2に
直接血管造影剤あるいは生理的食塩水を注入した
が、この発明は穴2内に血管に相当するパイプを
挿入し、このパイプ内に血管造影剤あるいは生理
的食塩水を注入したものを含むことはいうまでも
ない。 The relationship between the blood vessel diameter x and the logarithm of the relative exposure amount of X-rays is shown in a graph as shown in FIG. The horizontal axis is the blood vessel diameter X, and the vertical axis is the logarithm of the relative exposure amount of X-rays. As can be seen from this figure, a proportional relationship exists between the blood vessel diameter x and the logarithm E of the relative exposure amount of X-rays, indicating that equation (4) holds true. That is, it has become clear that the reference scale of the present invention can be used as a standard blood vessel during X-ray imaging of the vascular system. In the above embodiment, the angiographic agent or physiological saline was injected directly into the hole 2, but in this invention, a pipe corresponding to a blood vessel is inserted into the hole 2, and the angiographic agent or physiological saline is injected into the pipe. Needless to say, this includes those injected with saline.
以上説明した如く本発明によれば、生体とX線
吸収係数が等価な材質内にX線造影対象の血管に
対応するそれぞれ異なる径で、かつ各径が既知の
数種類の細長い断面が円形状の穴をあけ、これら
の各穴内に血管造影時に使用するときと等濃度の
血管造影剤あるいは血液と等価な生理的食塩水を
注入密封したので、X線写真画像から血管系を定
量化するに当り、従来の血管の径の測定方式等よ
りも測定の迅速化、簡便化が図れ、多量のX線写
真画像における血管径の定量化が高精度かつ高信
頼で測定することができる。また人工血管などを
使用することにより血管壁の定量化も可能とな
り、従来の方式に比べ、この簡便な基準スケール
を用いることにより、X線画像からの血管像の解
析の向上及び省力化に極めて有効である。 As explained above, according to the present invention, several types of elongated cross sections with different diameters and known diameters corresponding to the blood vessels to be imaged by X-ray are formed in a circular shape in a material whose X-ray absorption coefficient is equivalent to that of a living body. Holes were drilled and each hole was injected with an angiographic contrast agent at the same concentration as used during angiography or physiological saline equivalent to blood and sealed, so it was easy to quantify the vascular system from X-ray images. , measurement can be made faster and simpler than conventional blood vessel diameter measurement methods, and blood vessel diameters can be quantified with high precision and reliability in a large number of X-ray images. In addition, by using artificial blood vessels, it is possible to quantify the blood vessel wall, and compared to conventional methods, using this simple reference scale greatly improves the analysis of blood vessel images from X-ray images and saves labor. It is valid.
第1図は基準スケールの概要図、第2図a,b
は基準スケールの正面図と側面図、第3図は基準
スケール製造装置の概略図、第4図はX線撮影装
置の概略図、第5図はX線写真フイルム画像、第
6図は写真濃度とX線相対露光量の関係を示す
図、第7図はX線の透過モデル、第8図は血管径
とX線相対露光量の対数値の関係を示す図であ
る。
1:基準スケール本体、2:穴、3:フイル
タ、6:真空ポンプ、9:X線管球、10:フイ
ルムカセツテ。
Figure 1 is a schematic diagram of the standard scale, Figure 2 a, b
are front and side views of the reference scale, Fig. 3 is a schematic diagram of the reference scale manufacturing device, Fig. 4 is a schematic diagram of the X-ray photographing device, Fig. 5 is an X-ray photographic film image, and Fig. 6 is the photographic density. 7 is an X-ray transmission model, and FIG. 8 is a diagram showing the relationship between the blood vessel diameter and the logarithm of the X-ray relative exposure. 1: Reference scale body, 2: Hole, 3: Filter, 6: Vacuum pump, 9: X-ray tube, 10: Film cassette.
Claims (1)
価な材質内に、X線造影対象の血管に対応するそ
れぞれ異なる径で、かつ各径が既知の数種類の細
長い断面が円形状の穴をあけ、これらの各穴内に
血管造影時に使用するときと等濃度の血管造影剤
あるいは血液と等価な生理的食塩水を注入し、こ
れらの穴の両端を密封したことを特徴とする血管
系造影用基準スケール。1. In a material whose X-ray absorption coefficient is equivalent to that of the human body or a living body for experimental research, several types of elongated holes with circular cross-sections, each with a different diameter and each diameter known, corresponding to the blood vessels to be X-ray contrasted, are drilled. , a standard for vascular system imaging characterized by injecting into each of these holes an angiographic contrast agent at the same concentration as used during angiography or a physiological saline solution equivalent to blood, and sealing both ends of these holes. scale.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP57215916A JPS59105441A (en) | 1982-12-07 | 1982-12-07 | Reference scale for contrasting blood vessel |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP57215916A JPS59105441A (en) | 1982-12-07 | 1982-12-07 | Reference scale for contrasting blood vessel |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS59105441A JPS59105441A (en) | 1984-06-18 |
| JPS6410219B2 true JPS6410219B2 (en) | 1989-02-21 |
Family
ID=16680372
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP57215916A Granted JPS59105441A (en) | 1982-12-07 | 1982-12-07 | Reference scale for contrasting blood vessel |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS59105441A (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH0477323U (en) * | 1990-11-21 | 1992-07-06 |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS62142305U (en) * | 1986-02-28 | 1987-09-08 |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5016529U (en) * | 1973-06-05 | 1975-02-21 |
-
1982
- 1982-12-07 JP JP57215916A patent/JPS59105441A/en active Granted
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH0477323U (en) * | 1990-11-21 | 1992-07-06 |
Also Published As
| Publication number | Publication date |
|---|---|
| JPS59105441A (en) | 1984-06-18 |
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