WO2008065753A1 - Blood purification device - Google Patents

Blood purification device Download PDF

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Publication number
WO2008065753A1
WO2008065753A1 PCT/JP2007/001316 JP2007001316W WO2008065753A1 WO 2008065753 A1 WO2008065753 A1 WO 2008065753A1 JP 2007001316 W JP2007001316 W JP 2007001316W WO 2008065753 A1 WO2008065753 A1 WO 2008065753A1
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WO
WIPO (PCT)
Prior art keywords
blood
circuit
introduction part
pressure
opening
Prior art date
Application number
PCT/JP2007/001316
Other languages
French (fr)
Japanese (ja)
Inventor
Hiroshi Nimura
Yoshiro Ueda
Original Assignee
Nikkiso Company Limited
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 Nikkiso Company Limited filed Critical Nikkiso Company Limited
Publication of WO2008065753A1 publication Critical patent/WO2008065753A1/en

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Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61MDEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M1/00Suction or pumping devices for medical purposes; Devices for carrying-off, for treatment of, or for carrying-over, body-liquids; Drainage systems
    • A61M1/36Other treatment of blood in a by-pass of the natural circulatory system, e.g. temperature adaptation, irradiation ; Extra-corporeal blood circuits
    • A61M1/3621Extra-corporeal blood circuits
    • A61M1/3639Blood pressure control, pressure transducers specially adapted therefor

Definitions

  • the present invention relates to a blood purification apparatus in which a pressure measuring chain is connected in the middle of a blood circuit for circulating a patient's blood extracorporeally.
  • a hemodialysis apparatus having a blood circuit composed of a flexible tube that circulates the blood of a patient extracorporeally is used.
  • the blood circuit in this hemodialysis apparatus includes an arterial blood circuit in which an arterial puncture needle for collecting blood from a patient is attached to the tip, and a venous blood circuit in which a venous puncture needle for returning blood to the patient is attached to the tip.
  • the dialyzer is interposed between the arterial blood circuit and the venous blood circuit to purify the blood circulating outside the body.
  • the blood circuit (at least one of the arterial blood circuit and the venous blood circuit) is formed of a resin molded product having a large inner diameter accommodating space inside the blood circuit.
  • a drip chamber is connected.
  • a pressure monitor line is extended from the air layer side formed in the accommodating space, and a pressure measuring means is connected to the extended end. ing.
  • the blood pressure of the patient who is undergoing dialysis treatment can be monitored by the pressure monitor line together with the defoaming.
  • the drip chamber monitors the pressure of the blood while defoaming the blood circulating outside the body. Therefore, the liquid level in the accommodation space (the blood liquid level) by the air supplemented by the defoaming action The position of the surface has changed, making it difficult to accurately measure the pressure of blood circulating outside the body. Therefore, a separate level adjustment line is usually connected to the dripping chamber.
  • the level adjustment line is extended from the air layer side of the drip chamber, and a syringe or the like is connected to the front end, and air is sent to the air layer by the syringe.
  • a syringe or the like is connected to the front end, and air is sent to the air layer by the syringe.
  • Patent Document 1 Japanese Patent Laid-Open No. 2 0 06 _ 1 0 2 2 3 7
  • the drip chamber in the conventional blood purification apparatus requires a level adjustment line for adjusting the liquid level in addition to the pressure monitor line, a plurality of lines are extended from one chamber. As a result, handling was inconvenient and caused a connection error in each line.
  • the drip chamber is exclusively used for defoaming, and a chamber for measuring blood pressure (pressure measuring chamber) is provided separately from the drip chamber, but in this case, the pressure measuring chamber is circulated. When air bubbles are generated from the blood, the air level changes due to the air, making it difficult to accurately measure the blood pressure.
  • the present invention has been made in view of such circumstances, and a blood purification apparatus including a pressure measurement chamber capable of measuring a blood pressure more accurately while suppressing a change in liquid level. Is to provide.
  • the invention according to claim 1 includes a blood circuit including an arterial blood circuit and a venous blood circuit for extracorporeally circulating a patient's blood, a blood pump disposed in the arterial blood circuit, and the arterial side.
  • a blood purification unit that is connected between the blood circuit and the venous blood circuit and purifies blood flowing through the blood circuit; and a storage space that is connected in the middle of the blood circuit and has a predetermined capacity;
  • a pressure measuring chamber in which a pressure monitor line for measuring the pressure of blood flowing through the blood circuit is extended, and connected downstream of the connecting portion of the blood measuring circuit in the blood circuit
  • a blood purification apparatus comprising a dripping chamber for removing the blood of a patient flowing through the blood circuit.
  • a blood deriving unit for deriving the blood introduced from the blood introduction unit which covers the entire area of the opening of the blood introduction unit and opens.
  • the invention according to claim 2 is the blood purification apparatus according to claim 1, wherein the arterial blood circuit, the blood purification means, and the venous blood circuit are prefilled with a priming solution, and the pressure measurement
  • the working chamber is characterized in that, by driving the blood pump, a liquid layer is formed in which the upper part is composed of a priming liquid and the lower part is composed of blood.
  • the invention described in claim 3 is the blood purification apparatus according to claim 1 or 2, wherein the opening of the blood introduction part in the pressure measuring chamber enters into the opening of the blood guiding part. It is characterized by overlapping.
  • the invention according to claim 4 is the blood purification apparatus according to claim 1 or 2, wherein the clearance of a minute dimension between the blood introduction part and the blood lead-out part in the pressure measurement chamber is used. A mesh is formed.
  • the pressure measuring chamber is formed in the lower part of the accommodation space, and introduces blood while opening near the bottom surface of the accommodation space, and the blood introduction part.
  • the openings are extended to a position where the openings are opposed to each other through a clearance of a minute dimension, and open over substantially the entire area of the opening of the blood introduction section, and the blood introduced from the blood introduction section is derived. Since it has a blood outlet, the bubbles in the blood introduced from the blood inlet are reliably led out from the blood outlet. Therefore, it is possible to more accurately measure the blood pressure by suppressing the accumulation of bubbles in the storage space and suppressing the change in the liquid level.
  • the pressure measuring chamber is driven by the blood pump.
  • a liquid layer consisting of priming liquid at the upper part and blood at the lower part is formed. Can be avoided.
  • blood is only slightly accumulated in the lower part of the liquid layer in the accommodation space, the extracorporeal blood volume can be reduced and the burden on the patient can be reduced.
  • the blood introduction part in the pressure measuring chamber overlaps when the opening enters the opening of the blood outlet part, so that the blood introduction part is introduced from the blood introduction part. Air bubbles in the blood can be more reliably guided to the blood outlet, and the change in the liquid level can be more reliably suppressed to accurately measure the blood pressure.
  • the mesh is formed in the minute dimension clearance between the blood introduction part and the blood lead-out part in the pressure measurement chamber, the mesh is mixed in the accommodation space. Foreign matter or the like can be captured with a mesh, and it can be avoided that the foreign matter or the like is derived from the blood outlet and flows into the blood circuit.
  • the blood purification apparatus is for purifying a patient's blood while circulating it extracorporeally, and is applied to a dialysis apparatus used in dialysis treatment.
  • a dialyzer is mainly composed of a blood circuit 1 connected to a dialer 2 as a blood purification means, and a dialyzer body 6 for removing water while supplying dialysate to the dialyzer 2.
  • the blood circuit 1 is mainly composed of an arterial blood circuit 1 a and a venous blood circuit 1 b made of a flexible tube.
  • the arterial blood circuit 1 a and the venous blood Dialer 2 is connected between circuit 1 b.
  • the arterial blood circuit 1 a has an arterial puncture needle a connected to the tip thereof, and an iron-type blood pump 3, a pressure measuring chamber 4, and a defoaming drip chamber along the way 5 (arterial drip chamber) is installed and connected.
  • a physiological saline line 10 having a physiological saline drip chamber 9 is extended in the middle, and a saline bag 8 containing a physiological saline at the tip 8 Is connected.
  • a venous puncture needle b is connected to the distal end of the venous blood circuit 1b, and a drip chamber 12 (venous drip chamber) for removing bubbles and a bubble detector 11 are connected to the venous blood circuit 1b.
  • a drip chamber 12 venous drip chamber
  • the pressure measuring chamber 4 is connected between the site of connection with the physiological saline line 10 in the arterial blood circuit 1a and the site of the blood pump 3, and the drip chamber 5 Is connected downstream of the connection part of the pressure measuring chamber 4 and between the connection part of the blood pump 3 and the connection part of the dialyzer 2.
  • the bubble detector 11 is mainly composed of a sensor 1 1a for detecting bubbles and a clamp 1 1b for cutting off the venous blood circuit 1b when bubbles are detected.
  • reference numeral 1 2 denotes a syringe pump for administering a drug or the like to the blood flowing through the blood circuit 1.
  • physiological saline for example, saline / Kug 8
  • saline / Kug 8 is used as a priming solution in advance in the arterial blood circuit 1a, the blood flow path of the dialyzer 2 and the venous side blood circuit 1b.
  • the blood pump 3 is driven, the physiological saline flows into the arterial blood circuit. 1a The blood is gradually replaced from the tip.
  • the dialyzer 2 is formed with a blood introduction port 2a, a blood outlet port 2b, a dialysate inlet port 2c, and a dialysate outlet port 2d in its casing, Of these, the proximal end of the arterial blood circuit 1a is connected to the blood introduction port 2a, and the proximal end of the venous blood circuit 1b is connected to the blood outlet port 2b.
  • the dialysate introduction port 2 c and the dialysate outlet port 2 d are connected to a dialysate introduction line L 1 and a dialysate discharge line L 2 extending from the dialyzer body 6, respectively.
  • a plurality of hollow fibers are accommodated in the dialyzer 2, the inside of the hollow fibers is used as a blood flow path, and dialysis is performed between the outer peripheral surface of the hollow fibers and the inner peripheral surface of the casing. It is a liquid flow path.
  • a hollow fiber membrane is formed in the hollow fiber by forming a number of minute holes (pores) penetrating the outer peripheral surface and the inner peripheral surface, and impurities in the blood and the like are passed through the membrane in the dialysate. It is comprised so that it can permeate
  • a dual pump, a dewatering pump, etc. (not shown) are arranged, and in addition to the action of the dialyzer 2, the blood circuit 1 is circulated outside the body. Dialysis treatment can be performed. Further, a pressure gauge 7 is formed in the dialyzer body 6, and the pressure gauge 7 is connected to a pressure monitor line L 3 extending from the pressure measurement chamber 4 via a filter (not shown). Yes.
  • the pressure measuring chamber 4 is connected in the middle of the arterial blood circuit 1 a (blood circuit 1) and has a predetermined capacity of the accommodating space 4 a, and the arterial side from the accommodating space 4 a
  • the pressure monitor line L 3 for measuring the pressure of the blood flowing through the blood circuit 1 a is extended.
  • the pressure measuring chamber 4 has a housing space 4a formed in the case C, and a blood introduction part 4b formed in the lower part thereof, and a side surface. And a blood lead-out portion 4 c extending from the head.
  • the blood introduction part 4b is a part where blood flowing through the arterial blood circuit 1a can be introduced upward from below while opening upward in the vicinity of the bottom surface of the accommodation space 4a.
  • the blood outlet 4c extends to the position where the openings (4ba, 4be) face each other through the clearance of the minute dimension t with respect to the blood inlet 4b.
  • the blood introduction part 4 b opening 4 b Covers the entire area of a (see Fig. 3), and guides the blood introduced from the blood introduction part 4b out of the accommodation space 4a (that is, downstream of the arterial blood circuit 1a). .
  • the opening 4 ca of the blood outlet 4 c is set to be larger than the opening 4 ba of the blood introduction part 4 b, and the opening 4 ca passes above the opening 4 ba through a minute clearance. Covering (a state where the projected area of the opening 4 ba is entirely within the opening of the opening 4 ca), the blood led from the blood introduction part 4 b or physiological saline as a priming solution is not cleared. Most of the space is filled from the blood outlet 4c while being filled into the accommodation space 4a.
  • the arterial blood circuit 1 a, the blood flow path of the dialyzer 2 and the venous blood circuit 1 b are filled with physiological saline as a brimming solution, and then the arterial puncture needle a and the venous side are filled.
  • the patient is punctured with the puncture needle b and the blood pump 3 is driven.
  • the physiological saline is guided from the blood introduction part 4 b in the pressure measurement chamber 4, and as shown in FIG. 4, a single layer of physiological saline (a physiological saline layer) is contained in the accommodation space 4 a. ) Will be formed.
  • the extracorporeal blood volume can be reduced and the burden on the patient can be reduced.
  • the blood layer in the accommodation space 4a; S is the lower part of the physiological saline layer, so it is in direct contact with the air layer. It will not be. Therefore, it is possible to prevent blood in the blood layer; S from coming into contact with the air in the air layer, thereby preventing thrombus from being promoted or foaming.
  • the pressure measuring chamber 4 includes a blood introduction part 4b that introduces blood while opening in the vicinity of the bottom surface of the accommodation space 4a, and a clearance of a minute dimension t with respect to the blood introduction part 4b.
  • a blood introduction part 4b that introduces blood while opening in the vicinity of the bottom surface of the accommodation space 4a, and a clearance of a minute dimension t with respect to the blood introduction part 4b.
  • the bubbles contained in the blood introduced from the blood introduction part 4b have a property of flowing upward because the specific gravity is lighter than that of the blood, and move along the blood flow, so that the clearance It is avoided that the blood reaches the S side through the blood and is smoothly led out from the blood outlet 4c. Therefore, it is possible to suppress the accumulation of bubbles in the storage space 4a, and to suppress the change in the liquid level in the storage space 4a.
  • the air layer 4 a side and the pressure gauge 7 communicate with each other via the pressure monitor line L 3, and the value measured by the pressure gauge 7 is the arterial blood circuit 1 a ( This indicates the pressure of blood flowing through the upstream side of blood pump 3).
  • the blood pressure can be measured more accurately.
  • the pressure measuring chamber 4 exclusively measures the blood pressure on the artery side, and bubbles contained in the flowing blood are removed by the downstream drip chamber 5. Therefore, bubbles will reach the dialyzer 2 Can be avoided.
  • the blood purification apparatus is for purifying a patient's blood while circulating externally, and is applied to a dialysis apparatus used in dialysis treatment.
  • a dialysis apparatus is substantially the same as that shown in FIG. 1, and only the pressure measuring chamber connected to the arterial blood circuit 1a is different.
  • the same components as those in the previous embodiment are denoted by the same reference numerals, and detailed description thereof is omitted.
  • the pressure measuring chamber 4 ′ has an accommodation space 4 a formed in the case C, and the blood introduction part 4 formed in the lower part thereof. b 'and a blood outlet 4c' extending downward from the upper surface.
  • the blood introduction part 4 b ′ is a part where blood flowing through the arterial blood circuit 1 a can be introduced upward from below while opening upward near the bottom surface of the accommodation space 4 a.
  • the blood outlet 4c ' extends to a position where the openings of the blood inlet 4c' face each other through a clearance of a minute dimension t with respect to the blood inlet 4b '(the suspension of the present embodiment is drooping)
  • the blood introduction part 4 b ′ covers the entire opening (the diameter of the blood introduction part 4 b ′ is larger than the opening of the blood introduction part 4 c ′), and the blood introduction part 4
  • the blood introduced from b ′ is led out of the accommodation space 4a (that is, downstream of the arterial blood circuit 1a).
  • the opening of the blood introduction part 4 b ′ is configured to enter into the opening of the blood outlet part 4 c ′, and overlaps.
  • the pressure measuring chamber 4 ' is driven by the blood pump 3, so that the upper part is physiological saline (saline layer) and the lower part is blood (blood layer; S).
  • the bubbles contained in the blood derived from the blood deriving portion 4 c ′ reach the downstream drip chamber 5 (see FIG. 1), where the bubbles are removed.
  • the openings of the blood introduction part 4b 'and the blood lead-out part 4c' in the pressure measurement chamber 4 ' are overlapped, so that they are introduced from the blood introduction part 4b'.
  • the air bubbles in the blood can be more reliably guided to the blood outlet 4 c ′, and the change in the liquid level can be more reliably suppressed to accurately measure the blood pressure.
  • the blood purification apparatus is for purifying a patient's blood while circulating externally, and is applied to a dialysis apparatus used in dialysis treatment.
  • a dialysis apparatus is substantially the same as that shown in FIG. 1, and only the pressure measuring chamber connected to the arterial blood circuit 1a is different.
  • the same components as those in the previous embodiment are denoted by the same reference numerals, and detailed description thereof is omitted.
  • the pressure measuring chamber 4 As shown in Fig. 7, the pressure measuring chamber 4 "according to the present embodiment has an accommodation space 4a formed in the case C, and the blood introduction part 4 formed in the lower part thereof. b "and a blood outlet 4c" extending downward from the upper surface.
  • the blood inlet 4b opens upward near the bottom surface of the accommodating space 4a and In the site where blood flowing through the side blood circuit 1a can be introduced from below to above
  • the blood outlet 4c extends to a position where the openings of the blood inlet 4c" face each other through a clearance of a minute dimension t with respect to the blood inlet 4b "(in this embodiment, it is drooping)
  • the blood introduced from the blood introduction part 4 b" is stored outside the accommodation space 4 a.
  • a mesh 4 d is formed in the clearance between the opening of the blood introduction part 4 b ′′ and the opening of the blood outlet part 4 c ′′.
  • the pressure measuring chamber 4 is driven by the blood pump 3, so that the upper part is physiological saline (saline layer) and the lower part is blood (blood layer; S).
  • a double liquid layer consisting of the blood layer; the blood of S It only accumulates slightly in the lower part of 4a.
  • the bubbles contained in the blood derived from the blood deriving section 4 c ′′ reach the drip chamber 5 on the downstream side (see FIG. 1), where the bubbles are removed.
  • the mesh 4d is formed in the clearance of the minute dimension t between the blood introduction part 4b "and the blood outlet part 4c" in the pressure measurement chamber 4 ". Therefore, foreign matter mixed in the accommodation space 4a can be captured by the mesh 4d, and the foreign matter is prevented from being led out from the blood outlet 4c "and flowing into the blood circuit 1. can do.
  • the present invention is not limited to the above, and for example, the pressure measuring chamber to be connected to the blood circuit is shown in FIG. Is not extended into the storage space 4a, but only the blood outlet 4c is extended in the storage space 4a and the openings are opposed to each other, or as shown in FIG.
  • the clearance between 4 b and blood outlet 4 c may be formed by slit 4 e.
  • a single hole (such as a round hole) may be formed instead of the slit 4a.
  • the blood introduction part 4b and the blood lead-out part 4c are not limited to those in which the respective axes coincide with each other as in the above embodiment.
  • the axis of 4b and the axis of blood outlet 4c may be displaced substantially in parallel, or as shown in FIG. 11, either one (in this figure, blood introduction part 4b) is the other ( It may be extended with a predetermined angle with respect to the axis of the blood outlet 4c).
  • the blood outlet 4c is opened so as to cover substantially the entire opening of the blood inlet 4b (the projected area of the opening of the blood inlet 4b is equal to that of the blood outlet 4c). It is necessary to form so that the blood introduced from the blood introduction part 4 b is led out.
  • both the blood introduction part 4 b and the blood lead-out part 4 c may be configured to extend at a predetermined angle from the axis of the case C.
  • the blood outlet 4 c is extended in an inverted U shape in the accommodation space 4 a so that the opening faces the opening of the blood introduction part 4 b. Good.
  • the openings of each other face each other with a minute dimension clearance, the position of the clearance is set near the bottom surface of the accommodation space, and the blood outlet 4c It is necessary to cover almost the entire opening of part 4b.
  • the dialysis machine body 6 is applied to either a dialysis monitoring device that does not include a dialysate supply mechanism, or a personal dialyzer that includes a dialysate supply mechanism. You may do it.
  • the present invention can be applied to other blood purification apparatuses such as hemofiltration therapy and hemofiltration dialysis therapy in addition to hemodialysis therapy as in the embodiment.
  • a blood introduction part that is formed in the lower part of the accommodation space and introduces blood while opening in the vicinity of the bottom surface of the accommodation space, and the openings face each other with a minute dimension clearance with respect to the blood introduction part
  • a pressure measuring chamber having a blood lead-out part that extends to a position where the blood is introduced, covers substantially the entire opening of the blood introduction part, and leads out the blood introduced from the blood introduction part.
  • FIG. 1 is an overall schematic diagram showing a blood purification apparatus according to a first embodiment of the present invention.
  • FIG. 2 is a schematic cross-sectional view showing a pressure measurement chamber connected to a blood circuit in the blood purification apparatus.
  • FIG. 4 is a schematic diagram showing a state in which physiological saline (priming solution) is accommodated in the same pressure measurement chamber.
  • FIG. 5 is a schematic diagram showing a state in which blood is stored in addition to physiological saline (priming solution) in the same pressure measurement chamber.
  • FIG. 6 is a schematic cross-sectional view showing a pressure measuring chamber connected to the blood purification apparatus of the second embodiment of the present invention.
  • FIG. 7 is a schematic cross-sectional view showing a pressure measurement chamber connected to the blood purification apparatus of the third embodiment of the present invention.
  • FIG. 8 is a schematic cross-sectional view showing a pressure measurement chamber in still another embodiment of the present invention.
  • FIG. 9 is a schematic cross-sectional view showing a pressure measurement chamber in still another embodiment of the present invention.
  • FIG. 10 is a schematic cross-sectional view showing a pressure measurement chamber in still another embodiment of the present invention.
  • FIG. 11 is a schematic cross-sectional view showing a pressure measurement chamber in still another embodiment of the present invention.
  • FIG. 12 is a schematic cross-sectional view showing a pressure measurement chamber in still another embodiment of the present invention.
  • FIG. 13 is a schematic cross-sectional view showing a pressure measurement chamber in still another embodiment of the present invention.

Abstract

[PROBLEMS] To provide a blood purification device comprising a pressure measurement chamber which can suppress a change in a liquid level to measure the pressure of blood with higher accuracy. [MEANS FOR SOLVING PROBLEMS] A blood purification device comprising a blood circuit (1), a blood pump (3), a dialyzer (2) for purifying blood which flows through the blood circuit (1), a pressure measurement chamber (4) for measuring the pressure of blood which flows through the blood circuit (1), and a drip chamber (5) for removing bubbles from the blood which flows through the blood circuit (1). The pressure measurement chamber (4) is formed on the lower part in a storage space (4a) and comprises a blood introduction part (4b), which is open at a part near the bottom of the storage space (4a), for introducing blood, and a blood lead-out part (4c) for leading out the blood introduced through the blood introduction part (4b). The blood lead-out part (4c) extends toward the blood introduction part (4b) to a position, where the opening of the blood lead-out part (4c) faces the opening of the blood introduction part (4b) while providing a clearance of a very small size t, and the opening of the blood lead-out part (4c) covers substantially the whole area of the opening of the blood introduction part (4b).

Description

明 細 書  Specification
血液浄化装置  Blood purification equipment
技術分野  Technical field
[0001 ] 本発明は、 患者の血液を体外循環させる血液回路の途中に圧力測定用チヤ ン /くが接続された血液浄化装置に関するものである。  TECHNICAL FIELD [0001] The present invention relates to a blood purification apparatus in which a pressure measuring chain is connected in the middle of a blood circuit for circulating a patient's blood extracorporeally.
背景技術  Background art
[0002] 一般に、 血液浄化療法、 例えば透析治療においては、 患者の血液を体外循 環させるベく可撓性チューブから成る血液回路を具備した血液透析装置が使 用されている。 この血液透析装置における血液回路は、 患者から血液を採取 する動脈側穿刺針が先端に取り付けられた動脈側血液回路と、 患者に血液を 戻す静脈側穿刺針が先端に取り付けられた静脈側血液回路とから主に成り、 これら動脈側血液回路と静脈側血液回路との間にダイァライザを介在させ、 体外循環する血液の浄化を行っている。  In general, in blood purification therapy, for example, dialysis treatment, a hemodialysis apparatus having a blood circuit composed of a flexible tube that circulates the blood of a patient extracorporeally is used. The blood circuit in this hemodialysis apparatus includes an arterial blood circuit in which an arterial puncture needle for collecting blood from a patient is attached to the tip, and a venous blood circuit in which a venous puncture needle for returning blood to the patient is attached to the tip. The dialyzer is interposed between the arterial blood circuit and the venous blood circuit to purify the blood circulating outside the body.
[0003] また、 血液回路 (動脈側血液回路及び静脈側血液回路の少なくとも一方) の途中には、 当該血液回路における流路ょりも大きな内径の収容空間を内部 に有した樹脂成形品から成るドリップチャンバが接続されている。 このドリ ップチャンバには、 例えば特許文献 1にて開示されているように、 収容空間 に形成された空気層側から圧モニタラインが延設されており、 その延設端に 圧力計測手段が接続されている。 即ち、 除泡と共に圧モニタラインにて透析 治療中の患者の血圧を監視し得るように構成されているのである。  [0003] Further, the blood circuit (at least one of the arterial blood circuit and the venous blood circuit) is formed of a resin molded product having a large inner diameter accommodating space inside the blood circuit. A drip chamber is connected. In this dripping chamber, as disclosed in Patent Document 1, for example, a pressure monitor line is extended from the air layer side formed in the accommodating space, and a pressure measuring means is connected to the extended end. ing. In other words, the blood pressure of the patient who is undergoing dialysis treatment can be monitored by the pressure monitor line together with the defoaming.
[0004] 上記ドリップチャンバは、 体外循環する血液の除泡を行いつつ当該血液の 圧力を監視するものであるため、 除泡作用により補足された空気により収容 空間内の液面レベル (血液の液面の位置) が変化してしまい、 体外循環する 血液の圧力を正確に計測することが困難となっている。 従って、 通常、 ドリ ップチャンバには、 別個のレベル調整ラインが接続されている。  [0004] The drip chamber monitors the pressure of the blood while defoaming the blood circulating outside the body. Therefore, the liquid level in the accommodation space (the blood liquid level) by the air supplemented by the defoaming action The position of the surface has changed, making it difficult to accurately measure the pressure of blood circulating outside the body. Therefore, a separate level adjustment line is usually connected to the dripping chamber.
[0005] かかるレベル調整ラインは、 ドリップチャンバの気層側から延設され、 先 端にシリンジ等が接続されたもので、 当該シリンジによって空気層への空気 の挿入又は空気層からの空気の取り出しを行えば、 ドリップチャンバ内にお ける液面レベルを調整することができるようになっているものであり、 これ により体外循環する血液の圧力を正確に計測することができる。 [0005] The level adjustment line is extended from the air layer side of the drip chamber, and a syringe or the like is connected to the front end, and air is sent to the air layer by the syringe. By inserting or removing air from the air layer, the liquid level in the drip chamber can be adjusted, thereby accurately measuring the pressure of blood circulating outside the body. can do.
特許文献 1 :特開 2 0 0 6 _ 1 0 2 2 3 7号公報  Patent Document 1: Japanese Patent Laid-Open No. 2 0 06 _ 1 0 2 2 3 7
発明の開示  Disclosure of the invention
発明が解決しょうとする課題  Problems to be solved by the invention
[0006] しかしながら、 上記従来の血液浄化装置におけるドリップチャンバは、 圧 モニタラインに加え、 液面レベル調整のためのレベル調整ラインが必要とさ れるため、 一つのチャンバから複数のラインが延設されることとなり、 取り 扱いが不便であり各ラインの接続ミスを誘発する原因となっていた。 然るに 、 ドリップチャンバを除泡専用のものとし、 それとは別個に血液の圧力を測 定するチャンバ (圧力測定用チャンバ) を具備させることも考えられるが、 その場合、 当該圧力測定用チャンバ内を流通する血液から気泡が生じたとき 、 その空気により液面レベルが変化してしまい、 血液の圧力を正確に計測す ることが困難となってしまう。  However, since the drip chamber in the conventional blood purification apparatus requires a level adjustment line for adjusting the liquid level in addition to the pressure monitor line, a plurality of lines are extended from one chamber. As a result, handling was inconvenient and caused a connection error in each line. However, it is conceivable that the drip chamber is exclusively used for defoaming, and a chamber for measuring blood pressure (pressure measuring chamber) is provided separately from the drip chamber, but in this case, the pressure measuring chamber is circulated. When air bubbles are generated from the blood, the air level changes due to the air, making it difficult to accurately measure the blood pressure.
[0007] 本発明は、 このような事情に鑑みてなされたもので、 液面レベルの変化を 抑制して血液の圧力をより正確に測定することができる圧力測定用チャンバ を具備した血液浄化装置を提供することにある。  [0007] The present invention has been made in view of such circumstances, and a blood purification apparatus including a pressure measurement chamber capable of measuring a blood pressure more accurately while suppressing a change in liquid level. Is to provide.
課題を解決するための手段  Means for solving the problem
[0008] 請求項 1記載の発明は、 患者の血液を体外循環させる動脈側血液回路及び 静脈側血液回路から成る血液回路と、 前記動脈側血液回路に配設された血液 ポンプと、 前記動脈側血液回路と静脈側血液回路との間に接続され、 当該血 液回路を流れる血液を浄化する血液浄化手段と、 前記血液回路の途中に接続 されて所定容量の収容空間を有するとともに、 当該収容空間から当該血液回 路を流れる血液の圧力測定を行うための圧モニタラインが延設された圧力測 定用チャンバと、 前記血液回路における前記圧力測定用チャン/くの接続部位 よりも下流側に接続され、 当該血液回路を流れる患者の血液を除泡するドリ ップチャンバとを具備した血液浄化装置において、 前記圧力測定用チャンバ は、 前記収容空間の下部に形成され、 当該収容空間の底面近傍で開口しつつ 血液を導入する血液導入部と、 該血液導入部に対して微小寸法のクリアラン スを介して互いの開口が対向する位置まで延設されるとともに、 前記血液導 入部の開口の略全域を覆って開口し、 当該血液導入部から導入された血液を 導出する血液導出部とを有したものであることを特徴とする。 [0008] The invention according to claim 1 includes a blood circuit including an arterial blood circuit and a venous blood circuit for extracorporeally circulating a patient's blood, a blood pump disposed in the arterial blood circuit, and the arterial side. A blood purification unit that is connected between the blood circuit and the venous blood circuit and purifies blood flowing through the blood circuit; and a storage space that is connected in the middle of the blood circuit and has a predetermined capacity; A pressure measuring chamber in which a pressure monitor line for measuring the pressure of blood flowing through the blood circuit is extended, and connected downstream of the connecting portion of the blood measuring circuit in the blood circuit A blood purification apparatus comprising a dripping chamber for removing the blood of a patient flowing through the blood circuit. Is formed in the lower part of the accommodation space, and is opened near the bottom surface of the accommodation space, and introduces blood, and the openings are opposed to the blood introduction part through a micro dimension clearance. And a blood deriving unit for deriving the blood introduced from the blood introduction unit, which covers the entire area of the opening of the blood introduction unit and opens. To do.
[0009] 請求項 2記載の発明は、 請求項 1記載の血液浄化装置において、 前記動脈 側血液回路、 血液浄化手段及び静脈側血液回路には予めプライミング液が充 填されるとともに、 前記圧力測定用チャンバは、 前記血液ポンプの駆動によ り、 収容空間内において上部がプライミング液、 下部が血液から成る液層が 形成されることを特徴とする。  [0009] The invention according to claim 2 is the blood purification apparatus according to claim 1, wherein the arterial blood circuit, the blood purification means, and the venous blood circuit are prefilled with a priming solution, and the pressure measurement The working chamber is characterized in that, by driving the blood pump, a liquid layer is formed in which the upper part is composed of a priming liquid and the lower part is composed of blood.
[0010] 請求項 3記載の発明は、 請求項 1又は請求項 2記載の血液浄化装置におい て、 前記圧力測定用チャンバにおける血液導入部は、 その開口が前記血液導 出部の開口内に入り込むことによりオーバ一ラップして成ることを特徴とす る。  [0010] The invention described in claim 3 is the blood purification apparatus according to claim 1 or 2, wherein the opening of the blood introduction part in the pressure measuring chamber enters into the opening of the blood guiding part. It is characterized by overlapping.
[001 1 ] 請求項 4記載の発明は、 請求項 1又は請求項 2記載の血液浄化装置におい て、 前記圧力測定用チャンバにおける血液導入部と血液導出部との間の微小 寸法のクリアランスには、 メッシュが形成されたことを特徴とする。  [001 1] The invention according to claim 4 is the blood purification apparatus according to claim 1 or 2, wherein the clearance of a minute dimension between the blood introduction part and the blood lead-out part in the pressure measurement chamber is used. A mesh is formed.
発明の効果  The invention's effect
[0012] 請求項 1の発明によれば、 圧力測定用チャンバは、 収容空間の下部に形成 され、 当該収容空間の底面近傍で開口しつつ血液を導入する血液導入部と、 該血液導入部に対して微小寸法のクリアランスを介して互いの開口が対向す る位置まで延設されるとともに、 血液導入部の開口の略全域を覆って開口し 、 当該血液導入部から導入された血液を導出する血液導出部とを有している ので、 血液導入部から導入された血液中の気泡が確実に血液導出口から導出 されることとなる。 従って、 収容空間内に気泡が溜まってしまうのを抑制し 、 液面レベルの変化を抑制して血液の圧力をより正確に測定することができ る。  [0012] According to the invention of claim 1, the pressure measuring chamber is formed in the lower part of the accommodation space, and introduces blood while opening near the bottom surface of the accommodation space, and the blood introduction part. On the other hand, the openings are extended to a position where the openings are opposed to each other through a clearance of a minute dimension, and open over substantially the entire area of the opening of the blood introduction section, and the blood introduced from the blood introduction section is derived. Since it has a blood outlet, the bubbles in the blood introduced from the blood inlet are reliably led out from the blood outlet. Therefore, it is possible to more accurately measure the blood pressure by suppressing the accumulation of bubbles in the storage space and suppressing the change in the liquid level.
[0013] 請求項 2の発明によれば、 圧力測定用チャンバは、 血液ポンプの駆動によ り、 収容空間内において上部がプライミング液、 下部が血液から成る液層が 形成されるので、 血液が気層の空気に接触するのを回避して、 血栓が促進さ れたり或いは泡立ちが生じたりするのを回避することができる。 また、 血液 は収容空間における液層の下部に僅かに溜まるだけなので、 体外循環血液量 を減少させ、 患者への負担を軽減することができる。 [0013] According to the invention of claim 2, the pressure measuring chamber is driven by the blood pump. In the storage space, a liquid layer consisting of priming liquid at the upper part and blood at the lower part is formed. Can be avoided. Moreover, since blood is only slightly accumulated in the lower part of the liquid layer in the accommodation space, the extracorporeal blood volume can be reduced and the burden on the patient can be reduced.
[0014] 請求項 3の発明によれば、 圧力測定用チャンバにおける血液導入部は、 そ の開口が血液導出部の開口内に入り込むことによりオーバーラップして成る ので、 血液導入部から導入された血液中の気泡をより確実に血液導出口に導 き導出することができ、 液面レベルの変化をより確実に抑制して血液の圧力 を正確に測定することができる。  [0014] According to the invention of claim 3, the blood introduction part in the pressure measuring chamber overlaps when the opening enters the opening of the blood outlet part, so that the blood introduction part is introduced from the blood introduction part. Air bubbles in the blood can be more reliably guided to the blood outlet, and the change in the liquid level can be more reliably suppressed to accurately measure the blood pressure.
[0015] 請求項 4の発明によれば、 圧力測定用チャンバにおける血液導入部と血液 導出部との間の微小寸法のクリアランスには、 メッシュが形成されているの で、 収容空間内に混入した異物等をメッシュにて補足することができ、 その 異物等が血液導出部から導出して血液回路内へ流れてしまうのを回避するこ とができる。  [0015] According to the invention of claim 4, since the mesh is formed in the minute dimension clearance between the blood introduction part and the blood lead-out part in the pressure measurement chamber, the mesh is mixed in the accommodation space. Foreign matter or the like can be captured with a mesh, and it can be avoided that the foreign matter or the like is derived from the blood outlet and flows into the blood circuit.
発明を実施するための最良の形態  BEST MODE FOR CARRYING OUT THE INVENTION
[001 6] 以下、 本発明の実施形態について図面を参照しながら具体的に説明する。  [001 6] Hereinafter, embodiments of the present invention will be specifically described with reference to the drawings.
第 1の実施形態に係る血液浄化装置は、 患者の血液を体外循環させつつ浄 化するためのもので、 透析治療で使用される透析装置に適用されたものであ る。 かかる透析装置は、 図 1に示すように、 血液浄化手段としてのダイァラ ィザ 2が接続された血液回路 1、 ダイァライザ 2に透析液を供給しつつ除水 する透析装置本体 6から主に構成されている。 血液回路 1は、 同図に示すよ うに、 可撓性チューブから成る動脈側血液回路 1 a及び静脈側血液回路 1 b から主に構成されており、 これら動脈側血液回路 1 aと静脈側血液回路 1 b の間にダイァライザ 2が接続されている。  The blood purification apparatus according to the first embodiment is for purifying a patient's blood while circulating it extracorporeally, and is applied to a dialysis apparatus used in dialysis treatment. As shown in FIG. 1, such a dialyzer is mainly composed of a blood circuit 1 connected to a dialer 2 as a blood purification means, and a dialyzer body 6 for removing water while supplying dialysate to the dialyzer 2. ing. As shown in the figure, the blood circuit 1 is mainly composed of an arterial blood circuit 1 a and a venous blood circuit 1 b made of a flexible tube. The arterial blood circuit 1 a and the venous blood Dialer 2 is connected between circuit 1 b.
[001 7] 動脈側血液回路 1 aには、 その先端に動脈側穿刺針 aが接続されていると ともに、 途中にしごき型の血液ポンプ 3、 圧力測定用チャンバ 4及び除泡用 のドリップチャンバ 5 (動脈側ドリップチャンバ) が配設及び接続されてい る。 また、 動脈側血液回路 1 aの途中からは、 途中に生理食塩水用ドリップ チャンバ 9を有した生理食塩水ライン 1 0が延設されており、 先端には生理 食塩水を収容した生食バッグ 8が接続されている。 一方、 静脈側血液回路 1 bには、 その先端に静脈側穿刺針 bが接続されているとともに、 途中に除泡 用のドリップチャンバ 1 2 (静脈側ドリップチャンバ) 及び気泡検出器 1 1 が接続されている。 [001 7] The arterial blood circuit 1 a has an arterial puncture needle a connected to the tip thereof, and an iron-type blood pump 3, a pressure measuring chamber 4, and a defoaming drip chamber along the way 5 (arterial drip chamber) is installed and connected The Further, from the middle of the arterial blood circuit 1a, a physiological saline line 10 having a physiological saline drip chamber 9 is extended in the middle, and a saline bag 8 containing a physiological saline at the tip 8 Is connected. On the other hand, a venous puncture needle b is connected to the distal end of the venous blood circuit 1b, and a drip chamber 12 (venous drip chamber) for removing bubbles and a bubble detector 11 are connected to the venous blood circuit 1b. Has been.
[0018] 尚、 圧力測定用チャンバ 4は、 動脈側血液回路 1 aにおける生理食塩水ラ イン 1 0との接続部位と血液ポンプ 3の配設部位との間に接続されており、 ドリップチャンバ 5は、 当該圧力測定用チャンバ 4の接続部位より下流側で あって血液ポンプ 3の配設部位とダイァライザ 2の接続部位との間に接続さ れている。 また、 気泡検出器 1 1は、 気泡を検出するセンサ 1 1 aと気泡が 検出されたときに静脈側血液回路 1 bを遮断するクランプ 1 1 bとから主に 構成されたものである。 図 1中、 符号 1 2は、 血液回路 1を流れる血液に薬 剤等を投与するためのシリンジポンプを示している。  [0018] The pressure measuring chamber 4 is connected between the site of connection with the physiological saline line 10 in the arterial blood circuit 1a and the site of the blood pump 3, and the drip chamber 5 Is connected downstream of the connection part of the pressure measuring chamber 4 and between the connection part of the blood pump 3 and the connection part of the dialyzer 2. The bubble detector 11 is mainly composed of a sensor 1 1a for detecting bubbles and a clamp 1 1b for cutting off the venous blood circuit 1b when bubbles are detected. In FIG. 1, reference numeral 1 2 denotes a syringe pump for administering a drug or the like to the blood flowing through the blood circuit 1.
[001 9] そして、 動脈側穿刺針 a及び静脈側穿刺針 bを患者に穿刺した状態で、 血 液ポンプ 3を駆動させると、 患者の血液は、 動脈側血液回路 1 aを通ってダ ィァライザ 2に至り、 該ダイァライザ 2によって血液浄化が施され、 ドリツ プチャンバ 4で除泡がなされつつ静脈側血液回路 1 bを通って患者の体内に 戻る。 即ち、 患者の血液を血液回路 1にて体外循環させつつダイァライザ 2 にて浄化するのである。  [001 9] Then, when the blood pump 3 is driven with the patient punctured with the arterial puncture needle a and the venous puncture needle b, the patient's blood passes through the arterial blood circuit 1a and the dialyzer. 2, blood purification is performed by the dialyzer 2, and defoaming is performed in the dripping chamber 4, and then returned to the patient's body through the venous blood circuit 1 b. That is, the blood of the patient is purified by the dialyzer 2 while circulating outside the blood circuit 1.
[0020] 尚、 血液浄化治療前には、 予め動脈側血液回路 1 a、 ダイァライザ 2の血 液流路及び静脈側血液回路 1 bにプライミング液として生理食塩水 (例えば 生食/くッグ 8内の生理食塩水を血液回路 1内に流して血液の流路を洗浄した 後、 充填させたもの) が満たされており、 血液ポンプ 3を駆動させると、 当 該生理食塩水が動脈側血液回路 1 a先端から次第に血液と置換されることと なる。  [0020] Before blood purification treatment, physiological saline (for example, saline / Kug 8) is used as a priming solution in advance in the arterial blood circuit 1a, the blood flow path of the dialyzer 2 and the venous side blood circuit 1b. When the blood pump 3 is driven, the physiological saline flows into the arterial blood circuit. 1a The blood is gradually replaced from the tip.
[0021 ] ダイァライザ 2は、 その筐体部に、 血液導入ポート 2 a、 血液導出ポート 2 b、 透析液導入ポート 2 c及び透析液導出ポート 2 dが形成されており、 このうち血液導入ポート 2 aには動脈側血液回路 1 aの基端が、 血液導出ポ ート 2 bには静脈側血液回路 1 bの基端がそれぞれ接続されている。 また、 透析液導入ポート 2 c及び透析液導出ポート 2 dは、 透析装置本体 6から延 設された透析液導入ライン L 1及び透析液排出ライン L 2とそれぞれ接続さ れている。 [0021] The dialyzer 2 is formed with a blood introduction port 2a, a blood outlet port 2b, a dialysate inlet port 2c, and a dialysate outlet port 2d in its casing, Of these, the proximal end of the arterial blood circuit 1a is connected to the blood introduction port 2a, and the proximal end of the venous blood circuit 1b is connected to the blood outlet port 2b. The dialysate introduction port 2 c and the dialysate outlet port 2 d are connected to a dialysate introduction line L 1 and a dialysate discharge line L 2 extending from the dialyzer body 6, respectively.
[0022] ダイァライザ 2内には、 複数の中空糸が収容されており、 該中空糸内部が 血液の流路とされるとともに、 中空糸外周面と筐体部の内周面との間が透析 液の流路とされている。 中空糸には、 その外周面と内周面とを貫通した微少 な孔 (ポア) が多数形成されて中空糸膜を形成しており、 該膜を介して血液 中の不純物等が透析液内に透過し得るよう構成されている。  [0022] A plurality of hollow fibers are accommodated in the dialyzer 2, the inside of the hollow fibers is used as a blood flow path, and dialysis is performed between the outer peripheral surface of the hollow fibers and the inner peripheral surface of the casing. It is a liquid flow path. A hollow fiber membrane is formed in the hollow fiber by forming a number of minute holes (pores) penetrating the outer peripheral surface and the inner peripheral surface, and impurities in the blood and the like are passed through the membrane in the dialysate. It is comprised so that it can permeate | transmit.
[0023] —方、 透析装置本体 6内には、 図示しない複式ポンプや除水ポンプ等が配 設されており、 上記ダイァライザ 2の作用と併せて血液回路 1を体外循環す る血液に対して透析治療を施し得るようになつている。 更に、 透析装置本体 6内には、 圧力計 7が形成されており、 この圧力計 7は圧力測定用チャンバ 4から延設された圧モニタライン L 3と図示しないフィルタ等を介して接続 されている。  [0023] On the other hand, in the dialyzer main body 6, a dual pump, a dewatering pump, etc. (not shown) are arranged, and in addition to the action of the dialyzer 2, the blood circuit 1 is circulated outside the body. Dialysis treatment can be performed. Further, a pressure gauge 7 is formed in the dialyzer body 6, and the pressure gauge 7 is connected to a pressure monitor line L 3 extending from the pressure measurement chamber 4 via a filter (not shown). Yes.
[0024] ここで、 圧力測定用チャンバ 4は、 動脈側血液回路 1 a (血液回路 1 ) の 途中に接続されて所定容量の収容空間 4 aを有するとともに、 当該収容空間 4 aから当該動脈側血液回路 1 aを流れる血液の圧力測定を行うための圧モ 二タライン L 3が延設されたものである。 具体的には、 かかる圧力測定用チ ヤンバ 4は、 図 2に示すように、 ケース C内に収容空間 4 aが形成されてお り、 その下部に形成された血液導入部 4 bと、 側面から延設された血液導出 部 4 cとを有している。  Here, the pressure measuring chamber 4 is connected in the middle of the arterial blood circuit 1 a (blood circuit 1) and has a predetermined capacity of the accommodating space 4 a, and the arterial side from the accommodating space 4 a The pressure monitor line L 3 for measuring the pressure of the blood flowing through the blood circuit 1 a is extended. Specifically, as shown in FIG. 2, the pressure measuring chamber 4 has a housing space 4a formed in the case C, and a blood introduction part 4b formed in the lower part thereof, and a side surface. And a blood lead-out portion 4 c extending from the head.
[0025] 血液導入部 4 bは、 収容空間 4 aの底面近傍で上方を向いて開口しつつ、 動脈側血液回路 1 aを流れる血液を下方から上方に向けて導入し得る部位で ある。 また、 血液導出部 4 cは、 血液導入部 4 bに対して微小寸法 tのクリ ァランスを介して互いの開口 (4 b a、 4 b e ) が対向する位置まで延設 ( 本実施形態のものは屈曲形成) されるとともに、 血液導入部 4 bの開口 4 b aの全域を覆って開口し (図 3参照) 、 当該血液導入部 4 bから導入された 血液を収容空間 4 a外 (即ち、 動脈側血液回路 1 aの下流側) へ導出するも のである。 [0025] The blood introduction part 4b is a part where blood flowing through the arterial blood circuit 1a can be introduced upward from below while opening upward in the vicinity of the bottom surface of the accommodation space 4a. The blood outlet 4c extends to the position where the openings (4ba, 4be) face each other through the clearance of the minute dimension t with respect to the blood inlet 4b. The blood introduction part 4 b opening 4 b Covers the entire area of a (see Fig. 3), and guides the blood introduced from the blood introduction part 4b out of the accommodation space 4a (that is, downstream of the arterial blood circuit 1a). .
[0026] 即ち、 血液導出部 4 cの開口 4 c aの方が血液導入部 4 bの開口 4 b aよ り大きく設定されているとともに、 開口 4 c aが微小クリアランスを介して 開口 4 b aの上方を覆っている (開口 4 b aの投影面積が開口 4 c aの開口 内に全て収まっている状態) ため、 当該血液導入部 4 bから導かれた血液或 いはプライミング液としての生理食塩水は、 クリアランスを介して収容空間 4 a内に充填される一方、 そのほとんどが血液導出部 4 cから導出されるよ うになつているのである。  That is, the opening 4 ca of the blood outlet 4 c is set to be larger than the opening 4 ba of the blood introduction part 4 b, and the opening 4 ca passes above the opening 4 ba through a minute clearance. Covering (a state where the projected area of the opening 4 ba is entirely within the opening of the opening 4 ca), the blood led from the blood introduction part 4 b or physiological saline as a priming solution is not cleared. Most of the space is filled from the blood outlet 4c while being filled into the accommodation space 4a.
[0027] 次に、 上記実施形態の作用について説明する。  Next, the operation of the above embodiment will be described.
血液浄化治療前に、 予め動脈側血液回路 1 a、 ダイァライザ 2の血液流路 及び静脈側血液回路 1 bにブライミング液として生理食塩水を充填しておい た後、 動脈側穿刺針 a及び静脈側穿刺針 bを患者に穿刺して、 血液ポンプ 3 を駆動させる。 これにより、 圧力測定用チャンバ 4内において、 血液導入部 4 bから生理食塩水が導かれ、 図 4に示すように、 収容空間 4 a内に生理食 塩水単一の層 (生理食塩水層ひ) が形成されることとなる。  Before blood purification treatment, the arterial blood circuit 1 a, the blood flow path of the dialyzer 2 and the venous blood circuit 1 b are filled with physiological saline as a brimming solution, and then the arterial puncture needle a and the venous side are filled. The patient is punctured with the puncture needle b and the blood pump 3 is driven. As a result, the physiological saline is guided from the blood introduction part 4 b in the pressure measurement chamber 4, and as shown in FIG. 4, a single layer of physiological saline (a physiological saline layer) is contained in the accommodation space 4 a. ) Will be formed.
[0028] その後、 血液ポンプ 3の駆動に伴って血液回路 1内の生理食塩水が順次血 液と置換されていくと、 圧力測定用チャンバ 4内において、 血液導入部 4 b から血液が導かれることとなり、 図 5に示すように、 収容空間 4 a内に上部 が生理食塩水 (生理食塩水層ひ) 、 下部が血液 (血液層 ) から成る 2重の 液層が形成されることとなる。 このとき、 血液導入部 4 bの開口 4 b aと血 液導出部 4 cの開口 4 c aとの間のクリアランスが収容空間 4 aの底面近傍 であることから、 血液層; Sの血液は、 当該収容空間 4 aの下部に僅かに溜ま るだけである。  [0028] Thereafter, when the physiological saline in the blood circuit 1 is sequentially replaced with blood as the blood pump 3 is driven, blood is guided from the blood introduction part 4b in the pressure measurement chamber 4. Thus, as shown in FIG. 5, a double liquid layer is formed in the accommodation space 4a, the upper part being physiological saline (saline layer) and the lower part being blood (blood layer). . At this time, since the clearance between the opening 4 ba of the blood introduction part 4 b and the opening 4 ca of the blood outlet part 4 c is in the vicinity of the bottom surface of the accommodation space 4 a, the blood in the blood layer; It only accumulates slightly in the lower part of the accommodation space 4a.
[0029] 従って、 血液層; Sの血液を僅かな量に抑制できることから、 体外循環血液 量を減少させ、 患者への負担を軽減することができる。 また、 収容空間 4 a 内の血液層; Sは、 生理食塩水層ひの下部とされるため、 気層 と直接接触触 れることがない。 従って、 血液層; Sの血液が気層 の空気に接触するのを回 避して、 血栓が促進されたり或いは泡立ちが生じたりするのを回避すること ができる。 [0029] Therefore, since blood in the blood layer; S can be suppressed to a small amount, the extracorporeal blood volume can be reduced and the burden on the patient can be reduced. In addition, the blood layer in the accommodation space 4a; S is the lower part of the physiological saline layer, so it is in direct contact with the air layer. It will not be. Therefore, it is possible to prevent blood in the blood layer; S from coming into contact with the air in the air layer, thereby preventing thrombus from being promoted or foaming.
[0030] また、 圧力測定用チャンバ 4は、 収容空間 4 aの底面近傍で開口しつつ血 液を導入する血液導入部 4 bと、 該血液導入部 4 bに対して微小寸法 tのク リアランスを介して互いの開口が対向する位置まで延設されるとともに、 血 液導入部 4 bの開口の略全域を覆って開口し (血液導入部 4 bの開口の投影 面積が血液導出部 4 cの開口内に収まった状態) 、 当該血液導入部 4 bから 導入された血液を導出する血液導出部 4 cとを有しているので、 血液導入部 4 bから導入された血液中の気泡が確実に血液導出口 4 cから導出されるこ ととなる。  [0030] In addition, the pressure measuring chamber 4 includes a blood introduction part 4b that introduces blood while opening in the vicinity of the bottom surface of the accommodation space 4a, and a clearance of a minute dimension t with respect to the blood introduction part 4b. Through which the openings of the blood introduction part 4 b are covered and substantially the whole area of the opening of the blood introduction part 4 b is covered (the projected area of the opening of the blood introduction part 4 b is the blood outlet part 4 c). And the blood deriving unit 4 c for deriving the blood introduced from the blood introducing unit 4 b, so that bubbles in the blood introduced from the blood introducing unit 4 b It is surely derived from the blood outlet 4c.
[0031 ] 即ち、 血液導入部 4 bから導入された血液中に含有する気泡は、 血液より も比重が軽いため上方へ流れる性質を有し、 且つ、 血液の流れに沿って移動 するので、 クリアランスを介して血液層; S側へ至ることが回避され、 血液導 出部 4 cからスムーズに導出されるのである。 従って、 収容空間 4 a内に気 泡が溜まってしまうのを抑制し、 当該収容空間 4 a内の液面レベルの変化を 抑制することができる。  [0031] That is, the bubbles contained in the blood introduced from the blood introduction part 4b have a property of flowing upward because the specific gravity is lighter than that of the blood, and move along the blood flow, so that the clearance It is avoided that the blood reaches the S side through the blood and is smoothly led out from the blood outlet 4c. Therefore, it is possible to suppress the accumulation of bubbles in the storage space 4a, and to suppress the change in the liquid level in the storage space 4a.
[0032] この状態で、 気層 4 a側と圧力計 7とは、 圧モニタライン L 3を介して連 通することとなり、 当該圧力計 7により測定された値が動脈側血液回路 1 a (血液ポンプ 3より上流側) を流れる血液の圧力を示すこととなる。 しかし て、 本実施形態においては、 既述のように、 収容空間 4 a内の液面レベルの 変化が抑制されているので、 血液の圧力をより正確に測定することができる  In this state, the air layer 4 a side and the pressure gauge 7 communicate with each other via the pressure monitor line L 3, and the value measured by the pressure gauge 7 is the arterial blood circuit 1 a ( This indicates the pressure of blood flowing through the upstream side of blood pump 3). Thus, in the present embodiment, as described above, since the change in the liquid level in the accommodation space 4a is suppressed, the blood pressure can be measured more accurately.
[0033] 尚、 血液導出部 4 cから導出された血液に含まれる気泡は、 下流側のドリ ップチャンバ 5に至り、 そこで気泡が除去されることとなる。 このように、 本実施形態においては、 圧力測定用チャンバ 4は専ら動脈側の血液の圧力を 測定し、 その流れる血液に含まれる気泡は下流のドリップチャンバ 5で除去 されるようになつている。 よって、 ダイァライザ 2内に気泡が至ってしまう のを回避することができる。 [0033] It should be noted that the bubbles contained in the blood derived from the blood deriving unit 4c reach the downstream dripping chamber 5, where the bubbles are removed. Thus, in the present embodiment, the pressure measuring chamber 4 exclusively measures the blood pressure on the artery side, and bubbles contained in the flowing blood are removed by the downstream drip chamber 5. Therefore, bubbles will reach the dialyzer 2 Can be avoided.
[0034] 次に、 本発明の第 2の実施形態について説明する。  [0034] Next, a second embodiment of the present invention will be described.
本実施形態に係る血液浄化装置は、 先の実施形態と同様、 患者の血液を体 外循環させつつ浄化するためのもので、 透析治療で使用される透析装置に適 用されたものである。 かかる透析装置は、 図 1で示すものと略同様なものと され、 動脈側血液回路 1 aに接続される圧力測定用チャンバのみが異なるも のである。 尚、 先の実施形態と同一の構成要素には同一の符号を付すことと し、 その詳細な説明を省略する。  As in the previous embodiment, the blood purification apparatus according to this embodiment is for purifying a patient's blood while circulating externally, and is applied to a dialysis apparatus used in dialysis treatment. Such a dialysis apparatus is substantially the same as that shown in FIG. 1, and only the pressure measuring chamber connected to the arterial blood circuit 1a is different. The same components as those in the previous embodiment are denoted by the same reference numerals, and detailed description thereof is omitted.
[0035] 本実施形態に係る圧力測定用チャンバ 4 ' は、 図 6に示すように、 そのケ ース C内に収容空間 4 aが形成されており、 その下部に形成された血液導入 部 4 b ' と、 上面から下方に延設された血液導出部 4 c ' とを有している。 血液導入部 4 b ' は、 収容空間 4 aの底面近傍で上方を向いて開口しつつ、 動脈側血液回路 1 aを流れる血液を下方から上方に向けて導入し得る部位で  As shown in FIG. 6, the pressure measuring chamber 4 ′ according to the present embodiment has an accommodation space 4 a formed in the case C, and the blood introduction part 4 formed in the lower part thereof. b 'and a blood outlet 4c' extending downward from the upper surface. The blood introduction part 4 b ′ is a part where blood flowing through the arterial blood circuit 1 a can be introduced upward from below while opening upward near the bottom surface of the accommodation space 4 a.
[0036] また、 血液導出部 4 c ' は、 血液導入部 4 b ' に対して微小寸法 tのクリ ァランスを介して互いの開口が対向する位置まで延設 (本実施形態のものは 垂下) されるとともに、 血液導入部 4 b ' の開口の全域を覆って開口し (血 液導出部 4 b ' の開口の径が血液導入部 4 c ' の開口より大きい) 、 当該血 液導入部 4 b ' から導入された血液を収容空間 4 a外 (即ち、 動脈側血液回 路 1 aの下流側) へ導出するものである。 ここで、 血液導入部 4 b ' の開口 は、 血液導出部 4 c ' の開口内に入り込んで構成され、 オーバ一ラップして いる。 [0036] Further, the blood outlet 4c 'extends to a position where the openings of the blood inlet 4c' face each other through a clearance of a minute dimension t with respect to the blood inlet 4b '(the suspension of the present embodiment is drooping) The blood introduction part 4 b ′ covers the entire opening (the diameter of the blood introduction part 4 b ′ is larger than the opening of the blood introduction part 4 c ′), and the blood introduction part 4 The blood introduced from b ′ is led out of the accommodation space 4a (that is, downstream of the arterial blood circuit 1a). Here, the opening of the blood introduction part 4 b ′ is configured to enter into the opening of the blood outlet part 4 c ′, and overlaps.
[0037] かかる圧力測定用チャンバ 4 ' は、 先の実施形態と同様、 血液ポンプ 3を 駆動することにより、 上部が生理食塩水 (生理食塩水層ひ) 、 下部が血液 ( 血液層; S ) から成る 2重の液層が形成され、 血液層; Sの血液は、 当該収容空 間 4 aの下部に僅かに溜まるだけである。 尚、 血液導出部 4 c ' から導出さ れた血液に含まれる気泡は、 下流側のドリップチャンバ 5 (図 1参照) に至 り、 そこで気泡が除去されることとなる。 [0038] 本実施形態によれば、 圧力測定用チャンバ 4 ' における血液導入部 4 b ' と血液導出部 4 c ' の開口は、 オーバーラップして成るので、 血液導入部 4 b ' から導入された血液中の気泡をより確実に血液導出口 4 c ' に導き導出 することができ、 液面レベルの変化をより確実に抑制して血液の圧力を正確 に測定することができる。 [0037] As in the previous embodiment, the pressure measuring chamber 4 'is driven by the blood pump 3, so that the upper part is physiological saline (saline layer) and the lower part is blood (blood layer; S). A double liquid layer consisting of the blood layer; the blood of S; only slightly accumulates in the lower part of the accommodation space 4a. The bubbles contained in the blood derived from the blood deriving portion 4 c ′ reach the downstream drip chamber 5 (see FIG. 1), where the bubbles are removed. [0038] According to the present embodiment, the openings of the blood introduction part 4b 'and the blood lead-out part 4c' in the pressure measurement chamber 4 'are overlapped, so that they are introduced from the blood introduction part 4b'. The air bubbles in the blood can be more reliably guided to the blood outlet 4 c ′, and the change in the liquid level can be more reliably suppressed to accurately measure the blood pressure.
[0039] 次に、 本発明の第 3の実施形態について説明する。  [0039] Next, a third embodiment of the present invention will be described.
本実施形態に係る血液浄化装置は、 先の実施形態と同様、 患者の血液を体 外循環させつつ浄化するためのもので、 透析治療で使用される透析装置に適 用されたものである。 かかる透析装置は、 図 1で示すものと略同様なものと され、 動脈側血液回路 1 aに接続される圧力測定用チャンバのみが異なるも のである。 尚、 先の実施形態と同一の構成要素には同一の符号を付すことと し、 その詳細な説明を省略する。  As in the previous embodiment, the blood purification apparatus according to this embodiment is for purifying a patient's blood while circulating externally, and is applied to a dialysis apparatus used in dialysis treatment. Such a dialysis apparatus is substantially the same as that shown in FIG. 1, and only the pressure measuring chamber connected to the arterial blood circuit 1a is different. The same components as those in the previous embodiment are denoted by the same reference numerals, and detailed description thereof is omitted.
[0040] 本実施形態に係る圧力測定用チャンバ 4 " は、 図 7に示すように、 そのケ ース C内に収容空間 4 aが形成されており、 その下部に形成された血液導入 部 4 b " と、 上面から下方に延設された血液導出部 4 c " とを有している。 血液導入部 4 b " は、 収容空間 4 aの底面近傍で上方を向いて開口しつつ、 動脈側血液回路 1 aを流れる血液を下方から上方に向けて導入し得る部位で  [0040] As shown in Fig. 7, the pressure measuring chamber 4 "according to the present embodiment has an accommodation space 4a formed in the case C, and the blood introduction part 4 formed in the lower part thereof. b "and a blood outlet 4c" extending downward from the upper surface. The blood inlet 4b "opens upward near the bottom surface of the accommodating space 4a and In the site where blood flowing through the side blood circuit 1a can be introduced from below to above
[0041 ] また、 血液導出部 4 c " は、 血液導入部 4 b " に対して微小寸法 tのクリ ァランスを介して互いの開口が対向する位置まで延設 (本実施形態のものは 垂下) されるとともに、 血液導入部 4 b " の開口の全域を覆って開口し (両 開口の径が略同一且つ略同心) 、 当該血液導入部 4 b " から導入された血液 を収容空間 4 a外 (即ち、 動脈側血液回路 1 aの下流側) へ導出するもので ある。 ここで、 血液導入部 4 b " の開口と血液導出部 4 c " の開口との間の クリアランスには、 メッシュ 4 dが形成されている。 [0041] In addition, the blood outlet 4c "extends to a position where the openings of the blood inlet 4c" face each other through a clearance of a minute dimension t with respect to the blood inlet 4b "(in this embodiment, it is drooping) At the same time, the whole area of the opening of the blood introduction part 4 b "is covered (both openings have substantially the same diameter and are substantially concentric), and the blood introduced from the blood introduction part 4 b" is stored outside the accommodation space 4 a. (Ie, downstream of the arterial blood circuit 1a). Here, a mesh 4 d is formed in the clearance between the opening of the blood introduction part 4 b ″ and the opening of the blood outlet part 4 c ″.
[0042] かかる圧力測定用チャンバ 4 " は、 先の実施形態と同様、 血液ポンプ 3を 駆動することにより、 上部が生理食塩水 (生理食塩水層ひ) 、 下部が血液 ( 血液層; S ) から成る 2重の液層が形成され、 血液層; Sの血液は、 当該収容空 間 4 aの下部に僅かに溜まるだけである。 尚、 血液導出部 4 c " から導出さ れた血液に含まれる気泡は、 下流側のドリップチャンバ 5 (図 1参照) に至 り、 そこで気泡が除去されることとなる。 [0042] As in the previous embodiment, the pressure measuring chamber 4 "is driven by the blood pump 3, so that the upper part is physiological saline (saline layer) and the lower part is blood (blood layer; S). A double liquid layer consisting of the blood layer; the blood of S It only accumulates slightly in the lower part of 4a. The bubbles contained in the blood derived from the blood deriving section 4 c ″ reach the drip chamber 5 on the downstream side (see FIG. 1), where the bubbles are removed.
[0043] 本実施形態によれば、 圧力測定用チャンバ 4 " における血液導入部 4 b " と血液導出部 4 c " との間の微小寸法 tのクリアランスには、 メッシュ 4 d が形成されているので、 収容空間 4 a内に混入した異物等をメッシュ 4 dに て補足することができ、 その異物等が血液導出部 4 c " から導出して血液回 路 1内へ流れてしまうのを回避することができる。  [0043] According to the present embodiment, the mesh 4d is formed in the clearance of the minute dimension t between the blood introduction part 4b "and the blood outlet part 4c" in the pressure measurement chamber 4 ". Therefore, foreign matter mixed in the accommodation space 4a can be captured by the mesh 4d, and the foreign matter is prevented from being led out from the blood outlet 4c "and flowing into the blood circuit 1. can do.
[0044] 以上、 本実施形態について説明したが、 本発明は上記のものに限定されず 、 例えば血液回路に接続されるべき圧力測定用チャンバが、 図 8に示すよう に、 血液導入部 4 bを収容空間 4 a内に延設させず、 血液導出部 4 cのみを 収容空間 4 a内で延設させて、 互いの開口を対向させたもの、 或いは図 9に 示すように、 血液導入部 4 bと血液導出部 4 cとの間のクリアランスがスリ ット 4 eにて形成されたものとしてもよい。 尚、 スリット 4 aに代えて単な る孔 (丸孔等) を形成するようにしてもよい。  Although the present embodiment has been described above, the present invention is not limited to the above, and for example, the pressure measuring chamber to be connected to the blood circuit is shown in FIG. Is not extended into the storage space 4a, but only the blood outlet 4c is extended in the storage space 4a and the openings are opposed to each other, or as shown in FIG. The clearance between 4 b and blood outlet 4 c may be formed by slit 4 e. A single hole (such as a round hole) may be formed instead of the slit 4a.
[0045] また、 血液導入部 4 bと血液導出部 4 cは、 上記実施形態の如くそれぞれ の軸が互いに一致しているものに限定されず、 例えば図 1 0に示すように、 血液導入部 4 bの軸と血液導出部 4 cの軸とが略平行にずれたものとしても よく、 或いは図 1 1に示すように、 何れか一方 (同図においては血液導入部 4 b ) が他方 (同血液導出部 4 c ) の軸に対して所定角度傾斜して延設され ていてもよい。 但し、 この場合であっても、 血液導出部 4 cは、 血液導入部 4 bの開口の略全域を覆って開口し (血液導入部 4 bの開口の投影面積が血 液導出部 4 cの開口内に収まった状態) 、 当該血液導入部 4 bから導入され た血液を導出するよう形成する必要がある。  [0045] Further, the blood introduction part 4b and the blood lead-out part 4c are not limited to those in which the respective axes coincide with each other as in the above embodiment. For example, as shown in FIG. The axis of 4b and the axis of blood outlet 4c may be displaced substantially in parallel, or as shown in FIG. 11, either one (in this figure, blood introduction part 4b) is the other ( It may be extended with a predetermined angle with respect to the axis of the blood outlet 4c). However, even in this case, the blood outlet 4c is opened so as to cover substantially the entire opening of the blood inlet 4b (the projected area of the opening of the blood inlet 4b is equal to that of the blood outlet 4c). It is necessary to form so that the blood introduced from the blood introduction part 4 b is led out.
[0046] 更に、 図 1 2に示すように、 血液導入部 4 bと血液導出部 4 cの両方が、 ケース Cの軸から所定角度傾斜して延設されるよう構成してもよい。 また更 に、 図 1 3に示すように、 血液導出部 4 cを収容空間 4 a内において逆 U字 形に延設させ、 その開口を血液導入部 4 bの開口と対向させるようにしても よい。 尚、 何れの場合であっても、 互いの開口は微小寸法のクリアランスを 有して対向し、 そのクリアランスの位置が収容空間の底面近傍に設定される とともに、 血液導出部 4 cは、 血液導入部 4 bの開口の略全域を覆って開口 する必要がある。 Furthermore, as shown in FIG. 12, both the blood introduction part 4 b and the blood lead-out part 4 c may be configured to extend at a predetermined angle from the axis of the case C. Further, as shown in FIG. 13, the blood outlet 4 c is extended in an inverted U shape in the accommodation space 4 a so that the opening faces the opening of the blood introduction part 4 b. Good. In any case, the openings of each other face each other with a minute dimension clearance, the position of the clearance is set near the bottom surface of the accommodation space, and the blood outlet 4c It is necessary to cover almost the entire opening of part 4b.
[0047] 然るに、 本実施形態においては、 透析装置本体 6が透析液供給機構が内蔵 されない透析監視装置から成るもの、 或いは透析液供給機構が内蔵された個 人用透析装置の何れにも適用するようにしてもよい。 また、 本発明は、 実施 形態の如き血液透析療法の他、 血液濾過療法や血液濾過透析療法等、 他の血 液浄化装置に適用することができる。  [0047] However, in this embodiment, the dialysis machine body 6 is applied to either a dialysis monitoring device that does not include a dialysate supply mechanism, or a personal dialyzer that includes a dialysate supply mechanism. You may do it. Further, the present invention can be applied to other blood purification apparatuses such as hemofiltration therapy and hemofiltration dialysis therapy in addition to hemodialysis therapy as in the embodiment.
産業上の利用可能性  Industrial applicability
[0048] 収容空間の下部に形成され、 当該収容空間の底面近傍で開口しつつ血液を 導入する血液導入部と、 該血液導入部に対して微小寸法のクリアランスを介 して互いの開口が対向する位置まで延設されるとともに、 血液導入部の開口 の略全域を覆って開口し、 当該血液導入部から導入された血液を導出する血 液導出部とを有した圧力測定用チャンバが血液回路に接続された血液浄化装 置であれば、 外観形状が異なるもの或いは他の機能が付加されたもの等にも 適用することができる。  [0048] A blood introduction part that is formed in the lower part of the accommodation space and introduces blood while opening in the vicinity of the bottom surface of the accommodation space, and the openings face each other with a minute dimension clearance with respect to the blood introduction part A pressure measuring chamber having a blood lead-out part that extends to a position where the blood is introduced, covers substantially the entire opening of the blood introduction part, and leads out the blood introduced from the blood introduction part. As long as the blood purification device is connected to the device, it can also be applied to devices with different external shapes or with other functions added.
図面の簡単な説明  Brief Description of Drawings
[0049] [図 1 ]本発明の第 1の実施形態の血液浄化装置を示す全体模式図  [0049] FIG. 1 is an overall schematic diagram showing a blood purification apparatus according to a first embodiment of the present invention.
[図 2]同血液浄化装置における血液回路に接続された圧力測定用チャンバを示 す断面模式図  FIG. 2 is a schematic cross-sectional view showing a pressure measurement chamber connected to a blood circuit in the blood purification apparatus.
[図 3]図 2における I I I— I I I線断面図  [Fig.3] I I I— I I I line cross section
[図 4]同圧力測定用チャンバに生理食塩水 (プライミング液) が収容された状 態を示す模式図  FIG. 4 is a schematic diagram showing a state in which physiological saline (priming solution) is accommodated in the same pressure measurement chamber.
[図 5]同圧力測定用チャンバに生理食塩水 (プライミング液) に加え血液が収 容された状態を示す模式図  FIG. 5 is a schematic diagram showing a state in which blood is stored in addition to physiological saline (priming solution) in the same pressure measurement chamber.
[図 6]本発明の第 2の実施形態の血液浄化装置に接続された圧力測定用チャン バを示す断面模式図 [図 7]本発明の第 3の実施形態の血液浄化装置に接続された圧力測定用チャン バを示す断面模式図 FIG. 6 is a schematic cross-sectional view showing a pressure measuring chamber connected to the blood purification apparatus of the second embodiment of the present invention. FIG. 7 is a schematic cross-sectional view showing a pressure measurement chamber connected to the blood purification apparatus of the third embodiment of the present invention.
[図 8]本発明の更に他の実施形態における圧力測定用チャンバを示す断面模式 図  FIG. 8 is a schematic cross-sectional view showing a pressure measurement chamber in still another embodiment of the present invention.
[図 9]本発明の更に他の実施形態における圧力測定用チャンバを示す断面模式 図  FIG. 9 is a schematic cross-sectional view showing a pressure measurement chamber in still another embodiment of the present invention.
[図 10]本発明の更に他の実施形態における圧力測定用チャンバを示す断面模 式図  FIG. 10 is a schematic cross-sectional view showing a pressure measurement chamber in still another embodiment of the present invention.
[図 11 ]本発明の更に他の実施形態における圧力測定用チャンバを示す断面模 式図  FIG. 11 is a schematic cross-sectional view showing a pressure measurement chamber in still another embodiment of the present invention.
[図 12]本発明の更に他の実施形態における圧力測定用チャンバを示す断面模 式図  FIG. 12 is a schematic cross-sectional view showing a pressure measurement chamber in still another embodiment of the present invention.
[図 13]本発明の更に他の実施形態における圧力測定用チャンバを示す断面模 式図  FIG. 13 is a schematic cross-sectional view showing a pressure measurement chamber in still another embodiment of the present invention.
符号の説明 Explanation of symbols
1 血液回路  1 Blood circuit
1 a 動脈側血液回路  1 a Arterial blood circuit
1 b 静脈側血液回路  1 b Venous blood circuit
2 ダイァライザ (血液浄化手段)  2 Dializer (blood purification means)
3 血液ポンプ  3 Blood pump
4 圧力測定用チャンバ  4 Pressure measurement chamber
4 a 収容空間  4 a Containment space
4 b 血液導入部  4 b Blood introduction part
4 c 血液導出部  4 c Blood outlet
5 ドリップチャン /く (動脈側ドリップチャン /く)  5 Drip Chan / Ku (Arterial Drip Chan / Ku)
6 透析装置本体  6 Dialysis machine body
7 圧力計  7 Pressure gauge
8 生食バッグ 生理食塩水用ドリップチャンバ 8 Raw food bag Saline drip chamber
生理食塩水ライン Saline line
気泡検出器 Bubble detector
ドリップチャン/く (静脈側ドリップチャン /く) 圧モニタライン  Drip Chan / KU (Venous Drip Chan / KU) Pressure monitoring line
生理食塩水 (プライミング液) 層 Saline (priming solution) layer
血液層 Blood layer
気層 Air layer

Claims

請求の範囲 The scope of the claims
[1 ] 患者の血液を体外循環させる動脈側血液回路及び静脈側血液回路から成る 血液回路と、  [1] a blood circuit comprising an arterial blood circuit and a venous blood circuit for extracorporeally circulating the patient's blood;
前記動脈側血液回路に配設された血液ポンプと、  A blood pump disposed in the arterial blood circuit;
前記動脈側血液回路と静脈側血液回路との間に接続され、 当該血液回路を 流れる血液を浄化する血液浄化手段と、  Blood purification means connected between the arterial blood circuit and the venous blood circuit and purifying blood flowing through the blood circuit;
前記血液回路の途中に接続されて所定容量の収容空間を有するとともに、 当該収容空間から当該血液回路を流れる血液の圧力測定を行うための圧モニ タラインが延設された圧力測定用チャンバと、  A pressure measuring chamber which is connected in the middle of the blood circuit and has a predetermined volume of a storage space, and a pressure monitor line for measuring the pressure of blood flowing through the blood circuit from the storage space;
前記血液回路における前記圧力測定用チャンバの接続部位よりも下流側に 接続され、 当該血液回路を流れる患者の血液を除泡するドリップチャンバと を具備した血液浄化装置において、  A blood purification apparatus comprising: a drip chamber connected to a downstream side of a connection portion of the pressure measurement chamber in the blood circuit and defoaming a patient's blood flowing through the blood circuit;
前記圧力測定用チャンバは、  The pressure measuring chamber includes:
前記収容空間の下部に形成され、 当該収容空間の底面近傍で開口しつつ血 液を導入する血液導入部と、  A blood introduction part that is formed in a lower part of the accommodation space and introduces blood while opening near the bottom surface of the accommodation space;
該血液導入部に対して微小寸法のクリアランスを介して互いの開口が対向 する位置まで延設されるとともに、 前記血液導入部の開口の略全域を覆って 開口し、 当該血液導入部から導入された血液を導出する血液導出部と、 を有したものであることを特徴とする血液浄化装置。  The blood introduction part is extended to a position where the openings are opposed to each other through a minute dimension clearance, covers substantially the entire opening of the blood introduction part, and is introduced from the blood introduction part. A blood purification apparatus comprising: a blood deriving unit for deriving the blood.
[2] 前記動脈側血液回路、 血液浄化手段及び静脈側血液回路には予めプライミ ング液が充填されるとともに、 前記圧力測定用チャンバは、 前記血液ポンプ の駆動により、 収容空間内において上部がプライミング液、 下部が血液から 成る液層が形成されることを特徴とする請求項 1記載の血液浄化装置。  [2] The arterial blood circuit, the blood purification means, and the venous blood circuit are prefilled with a priming solution, and the pressure measuring chamber is primed at the top in the accommodation space by driving the blood pump. 2. The blood purification apparatus according to claim 1, wherein a liquid layer is formed in which the liquid and the lower part are blood.
[3] 前記圧力測定用チャンバにおける血液導入部は、 その開口が前記血液導出 部の開口内に入り込むことによりオーバ一ラップして成ることを特徴とする 請求項 1又は請求項 2記載の血液浄化装置。  [3] The blood purification according to claim 1 or 2, wherein the blood introduction part in the pressure measuring chamber overlaps with the opening of the blood introduction part entering the opening of the blood lead-out part. apparatus.
[4] 前記圧力測定用チャンバにおける血液導入部と血液導出部との間の微小寸 法のクリアランスには、 メッシュが形成されたことを特徴とする請求項 1又 は請求項 2記載の血液浄化装置。 [4] Minute dimension between blood introduction part and blood lead-out part in the pressure measuring chamber 3. The blood purification apparatus according to claim 1, wherein a mesh is formed in the legal clearance.
PCT/JP2007/001316 2006-11-29 2007-11-29 Blood purification device WO2008065753A1 (en)

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JP2006-321006 2006-11-29
JP2006321006A JP5078122B2 (en) 2006-11-29 2006-11-29 Blood purification equipment

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JP2005065888A (en) * 2003-08-22 2005-03-17 Nikkiso Co Ltd Blood vessel access observation method and medical apparatus

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