WO2021210188A1 - Catheter - Google Patents

Catheter Download PDF

Info

Publication number
WO2021210188A1
WO2021210188A1 PCT/JP2020/021738 JP2020021738W WO2021210188A1 WO 2021210188 A1 WO2021210188 A1 WO 2021210188A1 JP 2020021738 W JP2020021738 W JP 2020021738W WO 2021210188 A1 WO2021210188 A1 WO 2021210188A1
Authority
WO
WIPO (PCT)
Prior art keywords
contrast medium
catheter
thrombus
discharge
stent
Prior art date
Application number
PCT/JP2020/021738
Other languages
French (fr)
Japanese (ja)
Inventor
紘一郎 田代
Original Assignee
紘一郎 田代
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
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=78083867&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=WO2021210188(A1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by 紘一郎 田代 filed Critical 紘一郎 田代
Publication of WO2021210188A1 publication Critical patent/WO2021210188A1/en

Links

Images

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
    • A61M25/00Catheters; Hollow probes

Definitions

  • the present invention relates to a catheter inserted into a blood vessel.
  • a stent system including a wire and a stent connected to the distal side thereof has been used as an instrument for capturing a thrombus generated in a blood vessel.
  • This stent system is inserted into a blood vessel together with a catheter. After the thrombus is captured by the stent, the thrombus is recovered by being connected to the wire and the stent that has captured the thrombus is pulled out of the body (see, for example, Patent Document 1).
  • An object of the present invention is to provide a catheter capable of more accurately grasping the length of a thrombus by an X-ray transmission image.
  • the first invention is a catheter provided with a tubular catheter body, wherein the catheter body has a contrast medium discharge portion provided in a region on the distal end side when inserted into a blood vessel, and the contrast medium discharge portion.
  • the catheter comprises a plurality of discharge holes provided on the side surface of the portion, and the discharge holes are provided at least one at both ends in the central axial direction of the contrast medium discharge portion.
  • the plurality of discharge holes may be provided at equal intervals along the central axis direction of the contrast medium discharge portion.
  • the plurality of discharge holes may be provided at equal intervals along the circumferential direction of the contrast medium discharge portion.
  • the plurality of the discharge holes may be provided at positions facing each other in the radial direction of the contrast medium discharge portion.
  • At least one of the plurality of discharge holes may penetrate in a direction orthogonal to the central axis direction of the contrast medium discharge portion.
  • At least one of the plurality of discharge holes is such that the inner opening is located on the distal end side of the contrast medium discharge portion and the outer opening is located on the rear end side of the contrast medium discharge portion. It may penetrate in a direction diagonally intersecting the central axis direction of the contrast medium discharging portion.
  • the length of the thrombus can be grasped more accurately from the X-ray transmission image.
  • FIG. 2 is a cross-sectional view taken along the line AA of FIG.
  • FIG. 2 is a cross-sectional view taken along the line BB of FIG.
  • FIG. 2 is a cross-sectional view taken along the line CC of FIG.
  • It is a conceptual diagram of a catheter stent system 30. Is a schematic diagram showing a procedure for imaging a thrombus in a blood vessel with a catheter 1. Is a schematic diagram showing a procedure for imaging a thrombus in a blood vessel with a catheter 1.
  • FIG. 1 is a diagram showing the configuration of the catheter 1 of the first embodiment.
  • FIG. 2 is a side view of the contrast medium discharging unit 100.
  • FIG. 3 is a cross-sectional view taken along the line AA of FIG.
  • FIG. 4 is a cross-sectional view taken along the line BB of FIG.
  • FIG. 5 is a cross-sectional view taken along the line CC of FIG.
  • FIG. 1 is a diagram showing the configuration of the catheter 1 of the first embodiment.
  • FIG. 2 is a side view of the contrast medium discharging unit 100.
  • FIG. 3 is a cross-sectional view taken along the line AA of FIG.
  • FIG. 4 is a cross-sectional view taken along the line BB of FIG.
  • FIG. 5 is a cross-sectional view taken along the line CC of FIG.
  • the proximal end side (or the posterior end side) described later ) Is in the X1 direction, and the tip side is in the X2 direction.
  • the proximal end side is the X1 direction and the distal end side is the X2 direction.
  • the direction orthogonal to the central axis direction X is defined as the Y (Y1-Y2) direction.
  • the Y direction also coincides with the radial direction of the catheter body 10.
  • the vertical direction of the paper surface is the Z (Z1-Z2) direction.
  • the Z direction is a direction orthogonal to the XY direction shown in FIG.
  • the "-direction" is also appropriately referred to as a "-side”.
  • the catheter 1 includes a catheter body 10 and a hub 20.
  • the catheter 1 shown in FIG. 1 is used, for example, for imaging a thrombus formed in a cerebral blood vessel and for collecting a thrombus with a stent (described later).
  • the side where the catheter body 10 is inserted into the blood vessel is referred to as the "tip side” (X2 side)
  • the front side (hub 20 side) where the practitioner operates the catheter 1 is referred to as the "base end side” (the proximal end side).
  • the catheter 1 is used while being inserted into the guiding catheter, and is guided to a target site in the blood vessel together with the guide wire 11 (described later).
  • the catheter body 10 is a portion to be inserted into a blood vessel, and the entire catheter body 10 is formed in an elongated tubular shape.
  • the catheter body 10 has a spiral coil as a core material, a mesh-like braided coil, and the like coated with a resin layer, and has flexibility as a whole.
  • the outer diameter of the catheter body 10 is, for example, 0.55 to 2.1 mm.
  • the inner diameter of the catheter body 10 is, for example, 0.33 to 1.78 mm.
  • the catheter body 10 is provided with a contrast medium discharging portion 100 (described later) in a region on the distal end side when inserted into a blood vessel.
  • the hub 20 is a member provided on the proximal end side of the catheter body 10.
  • the inside of the hub 20 communicates with the catheter body 10.
  • the hub 20 is a portion that serves as an entrance when a contrast medium is injected into the catheter body 10 or a stent (described later) is inserted.
  • the hub 20 is also a portion that the practitioner grips when operating the catheter body 10 and the like.
  • the portion of the range S1 provided on the distal end side of the catheter main body 10 is the contrast medium discharging portion 100.
  • the range S1 is provided at the distal end side end of the discharge hole 110 provided on the most proximal end side (X1 side) and on the most distal end side (X2 side) in the central axial direction X of the contrast medium discharge portion 100. It is between the end of the discharge hole 110 on the distal end side.
  • the length of the range S1 of the contrast medium discharging portion 100 is set according to the length in the longitudinal direction of the thrombus to be imaged. For example, when the length of the thrombus to be imaged is assumed to be 50 mm, the length of the range S1 of the contrast medium discharging portion 100 is about 80 mm.
  • a catheter 1 catheter body 10 having a contrast medium discharging portion 100 suitable for the assumed length of the thrombus is selected.
  • the assumed length of the thrombus is comprehensively determined by the practitioner based on, for example, the site of the blood vessel into which the catheter 1 is inserted, the inner diameter, the blood flow rate, and the like.
  • the outer diameter and inner diameter of the contrast medium discharging portion 100 are the same as those of the catheter main body 10.
  • an example of the number, arrangement, diameter, etc. of the discharge holes 110 (described later) provided in the contrast medium discharge unit 100 will be specified, but these are the outer diameter, inner diameter, and length of the range S1 of the contrast agent discharge unit 100. Etc., it is appropriately selected.
  • each discharge hole 110 of the first embodiment penetrates in a direction orthogonal to the central axis direction X of the contrast medium discharge portion 100.
  • a tip opening 101 is provided on the tip side (X2 side) of the contrast medium discharging portion 100.
  • the stent 31 (described later) is pushed out from the tip opening 101.
  • the contrast medium injected into the catheter body 10 is discharged not only from the discharge hole 110 of the contrast medium discharge portion 100 but also from the tip opening 101.
  • a marker 102 is provided between the tip opening 101 and the contrast medium discharging portion 100.
  • the marker 102 is a ring-shaped member that serves as a mark for confirming the position of the catheter body 10 on the distal side.
  • the marker 102 is made of a metal material having X-ray impermeable property.
  • the plurality of discharge holes 110 are formed on the side surface of the contrast agent discharge unit 100 in the Y (Y1-Y2) direction and Z (Z1) along the central axis direction X of the contrast agent discharge unit 100.
  • the sides in the ⁇ Z2) direction are provided at equal intervals.
  • the 110s are arranged at equal intervals at a pitch of a distance L in the central axis direction X of the contrast medium discharging unit 100.
  • the distance L is, for example, 1 to 80 mm.
  • the diameter d of the discharge hole 110 (see FIG. 2) is, for example, 0.2 to 0.6 mm.
  • the discharge hole 110 can be formed, for example, by irradiating a region to be the contrast medium discharge portion 100 with a laser beam or piercing a hole punch or the like in the catheter main body 10.
  • four discharge holes 110 are provided on the side surfaces of the contrast medium discharge unit 100 in the Y (Y1-Y2) direction along the central axis direction X of the contrast medium discharge unit 100.
  • the discharge holes 110 provided on the side surface of the contrast medium discharge unit 100 in the Y (Y1-Y2) direction are the discharge holes provided on the side surface in the Z (Z1-Z2) direction in the central axis direction X of the contrast medium discharge unit 100. It is arranged alternately with the holes 110.
  • each discharge hole 110 provided on the side surface of the contrast medium discharge unit 100 in the Y (Y1-Y2) direction is the center of the contrast medium discharge unit 100 at each position in the central axial direction X, as shown in FIG. It is provided at positions facing each other in the radial direction with the shaft a in between. That is, each discharge hole 110 provided on the side surface of the contrast medium discharge unit 100 in the Y (Y1-Y2) direction is provided at two locations at each position in the central axial direction X, and is provided in the circumferential direction of the contrast medium discharge unit 100. They are arranged at 180 degree intervals along the CD. In other words, on the side surface of the contrast medium discharging unit 100 in the Y (Y1-Y2) direction, the discharge holes 110 are arranged at equal intervals along the circumferential CD of the contrast medium discharging unit 100.
  • each discharge hole 110 provided on the side surface of the contrast medium discharge unit 100 in the Z (Z1-Z2) direction is provided on the side surface in the Y (Y1-Y2) direction in the central axis direction X of the contrast medium discharge unit 100. It is arranged alternately with the discharge holes 110.
  • each discharge hole 110 provided on the side surface of the contrast medium discharge unit 100 in the Z (Z1-Z2) direction is the center of the contrast agent discharge unit 100 at each position in the central axial direction X, as shown in FIG. It is provided at positions facing each other in the radial direction with the shaft a in between. That is, each discharge hole 110 on the side surface of the contrast medium discharge unit 100 in the Z (Z1-Z2) direction is provided at two locations at each position in the central axial direction X, and is along the circumferential direction CD of the contrast medium discharge unit 100. They are arranged at intervals of 180 degrees.
  • the discharge holes 110 are arranged at equal intervals along the circumferential CD of the contrast medium discharge unit 100.
  • the discharge holes 110 on the side surface in the Y (Y1-Y2) direction and the side surface in the Z (Z1-Z2) direction of the contrast medium discharge unit 100 are provided at positions orthogonal to each other. There is.
  • FIG. 6 is a conceptual diagram of the catheter stent system 30.
  • the catheter stent system 30 includes a catheter body 10 (catheter 1) and a stent 31.
  • the catheter stent system 30 is a system in which the catheter 1 (see FIG. 1) and the stent 31 selected according to the length of the thrombus are combined.
  • the contrast medium discharging portion 100 provided on the distal end side (X2 side) of the catheter main body 10 is not shown.
  • the stent 31 is a member having a mesh pattern capable of accommodating a thrombus inside.
  • the stent 31 is inserted into the catheter body 10 in a reduced diameter state.
  • FIG. 6 schematically shows a cross section of the reduced diameter stent 31.
  • a wire 33 is connected to the proximal end portion 32 of the stent 31.
  • the wire 33 is sent to the distal end side (X2 side) when pushing the stent 31 to the target site in the blood vessel, and is pulled out to the proximal end side (X1 side) when the stent 31 is taken out of the body.
  • FIGS. 7A, 7B and 7C are schematic views showing a procedure for imaging a thrombus in a blood vessel with a catheter 1.
  • the guide wire 11 and the contrast medium discharge portion 100 in the thrombus BC are shown by solid lines in order to make the position of the discharge hole 110 easy to understand.
  • the proximal side close to the practitioner is referred to as D1 and the distal side away from the practitioner is referred to as D2 in the blood vessel BV.
  • various operations are performed when contrasting the thrombus, but the description will be omitted here.
  • the guide wire 11 is inserted into the patient's blood vessel BV, sent to the distal side D2, penetrates the inside of the thrombus BC which is the lesion site, and reaches the distal side of the thrombus BC.
  • the guide wire 11 does not have to penetrate the thrombus BC, and may be passed between the thrombus BC and the inner surface of the blood vessel BV, for example.
  • the position of thrombus BC can be roughly identified by performing head CT, MRI examination, cerebral angiography, etc. in advance. Whether or not the guide wire 11 has penetrated the inside of the thrombus BC is determined based on angiography performed by injecting a contrast medium from a guiding catheter or a microcatheter, information obtained by a preliminary examination, and the like.
  • the catheter body 10 is sent from the proximal side D1 to the distal side D2 so as to be extrapolated to the guide wire 11, and the tip of the catheter body 10 is inserted into the distal side D2 of the thrombus BC. To reach. Subsequently, the guide wire 11 is pulled out from the catheter body 10.
  • the contrast medium is injected from the proximal end side of the catheter body 10.
  • the contrast medium (small arrow in the figure) is discharged from each discharge hole 110 and the tip opening 101 of the contrast medium discharge unit 100.
  • the released contrast medium diffuses to the proximal side D1 and the distal side D2 of the thrombus BC and stays in the vicinity thereof.
  • reference numeral CA1 indicates a contrast region due to the contrast agent retained in D1 on the proximal side of thrombus BC.
  • Reference numeral CA2 indicates a contrast-enhanced region due to the contrast medium retained in D2 on the distal side of thrombus BC.
  • the contrast areas CA1 and CA2 have different brightness from other parts in the blood vessel (for example, thrombus BC), so that the practitioner can see the contrast areas CA1 and CA2 in the X-ray transmission image.
  • the positions of the proximal side D1 and the distal side D2 of the thrombus BC can be confirmed by visually recognizing.
  • the practitioner stops the injection of the contrast medium when the positions of the proximal side D1 and the distal side D2 of the thrombus BC are confirmed in the X-ray transmission image.
  • the practitioner can confirm the positions of the proximal side D1 and the distal side D2 of the thrombus BC in the contrast-enhanced areas CA1 and CA2, respectively, in the X-ray transmission image. Therefore, the practitioner can more accurately grasp the length of the thrombus BC by measuring the distance between the contrast-enhanced regions CA1 and CA2 in the X-ray transmission image. After this, the practitioner selects the stent 31 according to the length of the thrombus BC and collects the thrombus BC.
  • FIGS. 8A to 8D are schematic views showing the procedure for collecting a thrombus in a blood vessel by the catheter stent system 30.
  • thrombus BC is imaged and then thrombus is collected.
  • FIGS. 8A to 8D the reference numerals of the contrast medium discharge unit 100 (release hole 110) and the like are omitted.
  • the stent 31 is inserted into the catheter body 10 in a reduced diameter state, and the wire 33 is operated to send the stent 31 to the distal side D2 of the thrombus BC. Then, the tip of the stent 31 is positioned on the distal side D2 of the thrombus BC.
  • the stent 31 is pushed out from the tip of the catheter body 10 at the position of the thrombus BC and deployed. Specifically, by pulling the catheter body 10 from the position shown in FIG. 8A into the proximal side D1, the stent 31 is relatively pushed out from the catheter body 10 and deployed. The entire stent 31 is extruded from the catheter body 10.
  • the catheter body 10 is pulled into the proximal side D1 together with the wire 33.
  • the stent 31 that has captured the thrombus BC can be pulled out of the body.
  • the catheter stent system 30 By operating the catheter stent system 30 in the above procedure, the thrombus BC can be recovered from the inside of the blood vessel BV to the outside of the body.
  • a larger amount of the contrast medium can be diffused to the distal side D2 of the thrombus BC as compared with the case where the contrast medium is discharged from the tip end portion of the catheter body 10. .. Therefore, the practitioner can confirm the position of the proximal side D1 and the position of the distal side D2 of the thrombus BC by the contrast regions CA1 and CA2 in the X-ray transmission image. Therefore, the practitioner can more accurately grasp the length of the thrombus BC from the X-ray transmission image.
  • a stent 31 having the minimum necessary length suitable for the length of the thrombus BC when the practitioner selects a stent 31 having the minimum necessary length suitable for the length of the thrombus BC, when the stent 31 that has captured the thrombus is pulled out of the body, a longer stent is selected as compared with the case where the stent 31 is selected. Since the stent 31 is less likely to be caught on the blood vessel wall, the burden on the blood vessel wall can be reduced.
  • the discharge holes 110 are provided at equal intervals along the central axis direction X of the contrast medium discharge unit 100. According to this, since the contrast medium is evenly discharged in the central axis direction X of the contrast medium discharge unit 100, the length of the thrombus BC can be grasped more accurately in the X-ray transmission image. For example, even if the length of the thrombus BC is shorter than expected, the contrast medium is evenly released in the central axis direction X of the contrast medium discharging portion 100, so that the contrast medium BC is more located at the position of the distal side D2 of the thrombus BC. Contrast medium can be diffused.
  • the discharge holes 110 are arranged at equal intervals along the circumferential CD of the contrast medium discharge unit 100. Therefore, the contrast medium can be discharged more evenly in the circumferential CD of the contrast medium discharge unit 100.
  • the discharge holes 110 are provided at positions facing each other in the radial direction of the contrast medium discharge unit 100. Therefore, it is possible to prevent the contrast medium discharge portion 100 from being displaced in the direction orthogonal to the central axis a due to the reaction when the contrast medium is discharged from each discharge hole 110.
  • the contrast medium discharging unit 100 of the second embodiment has a different penetrating direction of the discharge holes 110 provided on the side surface from that of the first embodiment. Therefore, in FIG. 9, which will be described later, only the contrast medium discharging portion 100 (catheter body 10) is shown, and the entire catheter 1 is not shown. Further, in the description and drawings of the second embodiment, members and the like equivalent to those of the first embodiment are designated by the same reference numerals as those of the first embodiment, and duplicate description will be omitted.
  • FIG. 9 is a diagram showing the configuration of the contrast medium discharging unit 100 of the second embodiment.
  • FIG. 9 is a diagram corresponding to FIG. 2 of the first embodiment.
  • FIG. 9 only the discharge hole 110 provided on the side surface of the contrast medium discharge unit 100 in the Z (Z1-Z2) direction is shown.
  • the XX directions shown in FIG. 9 are based on FIG. 2.
  • the opening OP1 inside each of the discharging holes 110 is located on the tip side (X2 side) of the contrast medium discharging portion 100, and the outer opening OP2 is contrasted. It penetrates in a direction diagonally intersecting the central axis direction X so as to be located on the rear end side (X1 side) of the agent discharging portion 100.
  • the angle ⁇ at which the central axis b of each discharge hole 110 intersects the central axis a of the contrast medium discharge portion 100 is, for example, 30 ° to less than 90 °.
  • the stent 31 (see FIG. 6) inserted into the catheter body 10 in a reduced diameter state is placed on the distal end side of the contrast medium discharging unit 100.
  • the stent 31 is less likely to be caught in the opening OP1 of the discharge hole 110. Therefore, the stent 31 can be more smoothly deployed from the tip opening 101 of the contrast agent discharging portion 100.
  • the angle ⁇ at which the central axis b of each discharging hole 110 and the central axis a of the contrast medium discharging portion 100 intersect may be the same, or the angle ⁇ of the discharging hole 110 may be the same. It may be different depending on the position. Further, in the contrast medium discharge unit 100 of the second embodiment, the angle ⁇ at which the central axis b intersects with the central axis a of the contrast medium discharge unit 100 is 90 °, as in the discharge hole 110 of the first embodiment.
  • the hole 110 may be included.
  • the present invention is not limited to the first and second embodiments described above (hereinafter, also collectively referred to as “embodiments”), and the modified embodiments described later.
  • Various modifications and changes are possible, such as, which are also included within the technical scope of the present disclosure.
  • the effects described in the embodiments are merely a list of the most suitable effects resulting from the present disclosure, and are not limited to those described in the embodiments.
  • the above-described embodiment and the modified form described later can be used in combination as appropriate, but detailed description thereof will be omitted.
  • FIG. 10 is a cross-sectional view showing a modified example of the contrast medium discharging portion 100.
  • FIG. 10 corresponds to, for example, a cross-sectional view of FIG. 4 or FIG. 5 of the first embodiment.
  • the discharging holes 110 are provided at positions 120 ° apart from each other on the side surface of the contrast medium discharging portion 100. That is, the discharge holes 110 of the contrast medium discharge unit 100 shown in FIG. 10 are provided at three locations at each position in the central axial direction X, and are provided at intervals of 120 degrees along the circumferential CD of the contrast medium discharge unit 100. ing.
  • the discharge holes 110 of the contrast medium discharge unit 100 may be provided with 4 or more at each position in the central axial direction X, or different numbers of discharge holes 110 are provided at each position in the central axial direction X. You may be.
  • 11A and 11B are side views showing a modified example of the contrast medium discharging portion 100.
  • 11A and 11B correspond to, for example, the side views shown in FIG. 2 of the first embodiment.
  • the discharge holes 110 are provided at different pitches along the central axis direction X. Specifically, of the six discharge holes 110 provided along the central axis direction X of the contrast medium discharge portion 100, two discharge holes provided on the rear end side (X1 side) and the front end side (X2 side).
  • the holes 110a and 110b are arranged at a pitch of a distance L1.
  • the discharge holes 110b and the discharge holes 110c adjacent thereto are arranged at a pitch of a distance L2 (> L1).
  • the discharge holes 110c and the discharge holes 110d adjacent thereto are arranged at a pitch of a distance L3 (> L2).
  • the side surface on which the discharge hole 110 is provided may be in either the Y direction or the Z direction of the contrast medium discharge portion 100.
  • the discharge holes 110 are densely arranged on both ends in the central axial direction X, and the discharge holes 110 are sparsely arranged near the center. That is, it is considered that the contrast medium releasing portion 100 of the present embodiment is located on the proximal side (D1 side) and the distal side (D2 side) of the thrombus BC when it is penetrated through the thrombus BC of the assumed length.
  • the pitches of the discharge holes 110a and 110b are shortened, and the pitches of the discharge holes 110c and 110d, which are considered to be located near the middle of the thrombus BC, are lengthened.
  • the discharge holes that are considered to be located outside the thrombus BC are arranged at a short pitch, so that the contrast medium is imaged. More agent can be delivered to the proximal side (D1) and the distal side (D2) of thrombus BC. Further, according to the contrast medium discharge unit 100 of the present embodiment, when the contrast medium discharge unit 100 is penetrated through the thrombus BC, the discharge holes considered to be located near the middle of the thrombus BC are arranged at a longer pitch. Therefore, the amount of contrast medium released that is not involved in contrast can be reduced.
  • FIG. 11A an example in which discharge holes 110 are provided at six locations on the side surface of the contrast medium discharge portion 100 has been described. In the present embodiment, the positions where the discharge holes 110 are provided may be 5 or less, or 7 or more.
  • the contrast medium discharge unit 100 shown in FIG. 11B is provided with discharge holes 110e and 110f at one location on both ends in the central axial direction X, respectively. That is, the contrast medium discharge unit 100 of the present embodiment has a discharge hole 110a located on the proximal side (D1 side) of the thrombus BC and a distal side (D2) when the thrombus BC of the assumed length is penetrated. It has only a discharge hole 110b located on the side). For example, when the assumed length of the thrombus BC is 50 mm, the distance between the discharge holes 110a and 110b of the contrast medium discharge unit 100 of the present embodiment (or the range S1 in FIG. 2) is about 80 mm.
  • contrast medium releasing section 100 of the present embodiment when the contrast medium releasing section 100 is penetrated through the thrombus BC, more contrast medium is applied to the proximal side (D1) and the distal side (D2) of the thrombus BC. Can be reached. Further, according to the contrast medium discharging unit 100 of the present embodiment, when the contrast medium discharging unit 100 is penetrated through the thrombus BC, a discharge hole is not provided at a position considered to be near the middle of the thrombus BC. The amount of contrast medium released that is not involved in contrast can be further reduced.
  • a contrast medium discharging portion 100 separate from the catheter main body 10 may be attached to the tip of the catheter main body 10.
  • the catheter body 10 may be pulled out of the body and another catheter body 10 into which the reduced-diameter stent 31 is inserted may be inserted.
  • the contrast medium discharging portion 100 of the catheter body 10 for contrast medium may have a configuration in which the distal end side (X2 side) is sealed.

Abstract

Provided is a catheter with which it is possible to more accurately identify the length of a blood clot using an X-ray transmission image. A catheter body 10 of a catheter 1 comprises a contrast medium release section 100 provided in a region at a distal end side when inserted into a blood vessel, and a plurality of release holes 110 provided in a side surface of the contrast medium release section 100. At least one release hole 110 is provided in each end of the contrast medium release section 100 in a central axis direction X.

Description

カテーテルcatheter
 本発明は、血管内に挿入されるカテーテルに関する。 The present invention relates to a catheter inserted into a blood vessel.
 従来、血管内に発生した血栓を捕捉するための器具として、ワイヤと、その遠位側に連結されたステントとを備えるステント・システムが用いられている。このステント・システムは、カテーテルと共に血管内に挿入される。ステントにより血栓を捕捉した後、ワイヤに連結され且つ血栓を捕捉したステントが体外に引き出されることにより、血栓が回収される(例えば、特許文献1参照)。 Conventionally, a stent system including a wire and a stent connected to the distal side thereof has been used as an instrument for capturing a thrombus generated in a blood vessel. This stent system is inserted into a blood vessel together with a catheter. After the thrombus is captured by the stent, the thrombus is recovered by being connected to the wire and the stent that has captured the thrombus is pulled out of the body (see, for example, Patent Document 1).
特開2019-005587号公報Japanese Unexamined Patent Publication No. 2019-005587
 ステントにより血栓を回収する場合、あらかじめ血栓の長さに適したステントを選択しておく必要がある。従来、ステントを血栓の部位に送り込む前に、カテーテルの先端から造影剤(X線不透過)を血栓に放出して、X線透過の画像により血栓の位置、長さを把握することが行われている。しかし、従来の造影用のカテーテルでは、先端部から放出された造影剤が血栓の遠位側の端に届きにくいため、X線透過の画像により血栓の長さを正確に把握することが難しいという課題がある。このような課題を解決するため、例えば、より長いステントを選択することも考えられる。しかし、長いステントを使用した場合、血栓を捕捉したステントを体外に引き出した際に、ステントが血管壁に引っ掛かりやすくなるため、血管壁への負担が増大する。 When collecting a thrombus with a stent, it is necessary to select a stent suitable for the length of the thrombus in advance. Conventionally, before the stent is sent to the thrombus site, a contrast medium (X-ray opaque) is discharged from the tip of the catheter into the thrombus, and the position and length of the thrombus are grasped by an X-ray transmission image. ing. However, with conventional catheters for contrast media, it is difficult for the contrast medium released from the tip to reach the distal end of the thrombus, so it is difficult to accurately grasp the length of the thrombus from an X-ray transmission image. There are challenges. In order to solve such a problem, for example, it is conceivable to select a longer stent. However, when a long stent is used, when the stent that has captured the thrombus is pulled out of the body, the stent is likely to be caught on the blood vessel wall, which increases the burden on the blood vessel wall.
 本発明の目的は、X線透過の画像により血栓の長さを、より正確に把握できるカテーテルを提供することにある。 An object of the present invention is to provide a catheter capable of more accurately grasping the length of a thrombus by an X-ray transmission image.
 第1の発明は、筒状のカテーテル本体を備えるカテーテルであって、前記カテーテル本体は、血管内へ挿入される際に先端側となる領域に設けられた造影剤放出部と、前記造影剤放出部の側面に設けられた複数の放出孔と、を備え、前記放出孔は、前記造影剤放出部の中心軸方向の両端部に、少なくとも1つずつ設けられているカテーテルに関する。 The first invention is a catheter provided with a tubular catheter body, wherein the catheter body has a contrast medium discharge portion provided in a region on the distal end side when inserted into a blood vessel, and the contrast medium discharge portion. The catheter comprises a plurality of discharge holes provided on the side surface of the portion, and the discharge holes are provided at least one at both ends in the central axial direction of the contrast medium discharge portion.
 上記発明において、複数の前記放出孔は、前記造影剤放出部の中心軸方向に沿って等間隔に設けられていてもよい。 In the above invention, the plurality of discharge holes may be provided at equal intervals along the central axis direction of the contrast medium discharge portion.
 上記発明において、複数の前記放出孔は、前記造影剤放出部の周方向に沿って等間隔に設けられていてもよい。 In the above invention, the plurality of discharge holes may be provided at equal intervals along the circumferential direction of the contrast medium discharge portion.
 上記発明において、複数の前記放出孔は、前記造影剤放出部の径方向の対向する位置に設けられていてもよい。 In the above invention, the plurality of the discharge holes may be provided at positions facing each other in the radial direction of the contrast medium discharge portion.
 上記発明において、複数の前記放出孔の少なくとも1つは、前記造影剤放出部の中心軸方向と直交する方向に貫通していてもよい。 In the above invention, at least one of the plurality of discharge holes may penetrate in a direction orthogonal to the central axis direction of the contrast medium discharge portion.
 上記発明において、複数の前記放出孔の少なくとも1つは、内側の開口が前記造影剤放出部の先端側に位置し、外側の開口が前記造影剤放出部の後端側に位置するように、前記造影剤放出部の中心軸方向と斜めに交差する方向に貫通していてもよい。 In the above invention, at least one of the plurality of discharge holes is such that the inner opening is located on the distal end side of the contrast medium discharge portion and the outer opening is located on the rear end side of the contrast medium discharge portion. It may penetrate in a direction diagonally intersecting the central axis direction of the contrast medium discharging portion.
 本発明に係るカテーテルによれば、X線透過の画像により血栓の長さを、より正確に把握できる。 According to the catheter according to the present invention, the length of the thrombus can be grasped more accurately from the X-ray transmission image.
第1実施形態のカテーテル1の構成を示す図である。It is a figure which shows the structure of the catheter 1 of 1st Embodiment. 造影剤放出部100の側面図である。It is a side view of the contrast medium discharge part 100. 図2のA-A線断面図である。FIG. 2 is a cross-sectional view taken along the line AA of FIG. 図2のB-B線断面図である。FIG. 2 is a cross-sectional view taken along the line BB of FIG. 図2のC-C線断面図である。FIG. 2 is a cross-sectional view taken along the line CC of FIG. カテーテル・ステント・システム30の概念図である。It is a conceptual diagram of a catheter stent system 30. は、カテーテル1により血管内の血栓を造影する手順を示す模式図である。Is a schematic diagram showing a procedure for imaging a thrombus in a blood vessel with a catheter 1. は、カテーテル1により血管内の血栓を造影する手順を示す模式図である。Is a schematic diagram showing a procedure for imaging a thrombus in a blood vessel with a catheter 1. は、カテーテル1により血管内の血栓を造影する手順を示す模式図である。Is a schematic diagram showing a procedure for imaging a thrombus in a blood vessel with a catheter 1. は、カテーテル・ステント・システム30により血管内の血栓を回収する手順を示す模式図である。Is a schematic diagram showing a procedure for collecting a thrombus in a blood vessel by a catheter stent system 30. は、カテーテル・ステント・システム30により血管内の血栓を回収する手順を示す模式図である。Is a schematic diagram showing a procedure for collecting a thrombus in a blood vessel by a catheter stent system 30. は、カテーテル・ステント・システム30により血管内の血栓を回収する手順を示す模式図である。Is a schematic diagram showing a procedure for collecting a thrombus in a blood vessel by a catheter stent system 30. は、カテーテル・ステント・システム30により血管内の血栓を回収する手順を示す模式図である。Is a schematic diagram showing a procedure for collecting a thrombus in a blood vessel by a catheter stent system 30. 第2実施形態の造影剤放出部100の構成を示す図である。It is a figure which shows the structure of the contrast medium discharge part 100 of 2nd Embodiment. 造影剤放出部100の変形例を示す断面図である。It is sectional drawing which shows the modification of the contrast medium discharge part 100. は、造影剤放出部100の変形例を示す側面図である。Is a side view showing a modified example of the contrast medium discharging unit 100. は、造影剤放出部100の変形例を示す側面図である。Is a side view showing a modified example of the contrast medium discharging unit 100.
 以下、本発明に係るカテーテルの実施形態について説明する。なお、本明細書に添付した図面は、いずれも模式図であり、理解しやすさ等を考慮して、各部の形状、縮尺、縦横の寸法比等を、実物から変更又は誇張している。また、図面においては、部材の断面を示すハッチングを適宜に省略する。
 本明細書等において、形状、幾何学的条件、これらの程度を特定する用語、例えば、「平行」、「直交」、「方向」等の用語については、その用語の厳密な意味に加えて、ほぼ平行、ほぼ直交等とみなせる程度の範囲、概ねその方向とみなせる範囲を含む。
Hereinafter, embodiments of the catheter according to the present invention will be described. The drawings attached to the present specification are all schematic drawings, and the shape, scale, aspect ratio, etc. of each part are changed or exaggerated from the actual product in consideration of ease of understanding. Further, in the drawings, hatching indicating a cross section of the member is appropriately omitted.
In the present specification and the like, terms that specify the shape, geometric conditions, and their degrees, such as "parallel", "orthogonal", and "direction", are used in addition to the strict meaning of the terms. It includes a range that can be regarded as almost parallel, almost orthogonal, etc., and a range that can be regarded as being in that direction.
[第1実施形態]
 図1は、第1実施形態のカテーテル1の構成を示す図である。図2は、造影剤放出部100の側面図である。図3は、図2のA-A線断面図である。図4は、図2のB-B線断面図である。図5は、図2のC-C線断面図である。
 本明細書では、図2等に示すように、造影剤放出部100の中心軸aと平行な方向(以下、「中心軸方向X」ともいう)において、後述する基端側(又は後端側)をX1方向、先端側をX2方向とする。なお、カテーテル本体10の長手方向についても、基端側をX1方向、先端側をX2方向とする。本明細書では、図2に示す造影剤放出部100において、中心軸方向Xと直交する方向をY(Y1-Y2)方向とする。Y方向は、カテーテル本体10の径方向とも一致する。また、本明細書では、図3に示す造影剤放出部100において、紙面の上下方向をZ(Z1-Z2)方向とする。Z方向は、図2に示すX-Y方向と直交する方向である。更に、本明細書では、「~方向」を、適宜に「~側」ともいう。
[First Embodiment]
FIG. 1 is a diagram showing the configuration of the catheter 1 of the first embodiment. FIG. 2 is a side view of the contrast medium discharging unit 100. FIG. 3 is a cross-sectional view taken along the line AA of FIG. FIG. 4 is a cross-sectional view taken along the line BB of FIG. FIG. 5 is a cross-sectional view taken along the line CC of FIG.
In the present specification, as shown in FIG. 2 and the like, in a direction parallel to the central axis a of the contrast medium discharging portion 100 (hereinafter, also referred to as “central axis direction X”), the proximal end side (or the posterior end side) described later ) Is in the X1 direction, and the tip side is in the X2 direction. Regarding the longitudinal direction of the catheter body 10, the proximal end side is the X1 direction and the distal end side is the X2 direction. In the present specification, in the contrast medium discharging unit 100 shown in FIG. 2, the direction orthogonal to the central axis direction X is defined as the Y (Y1-Y2) direction. The Y direction also coincides with the radial direction of the catheter body 10. Further, in the present specification, in the contrast medium discharging unit 100 shown in FIG. 3, the vertical direction of the paper surface is the Z (Z1-Z2) direction. The Z direction is a direction orthogonal to the XY direction shown in FIG. Further, in the present specification, the "-direction" is also appropriately referred to as a "-side".
(カテーテル1)
 図1に示すように、カテーテル1は、カテーテル本体10と、ハブ20と、を備えている。
 図1に示すカテーテル1は、例えば、脳血管内に生じた血栓の造影、ステント(後述)による血栓の回収に用いられる。本明細書では、カテーテル本体10が血管内に挿入される側を「先端側」(X2側)といい、施術者がカテーテル1を操作する手前側(ハブ20側)を「基端側」(X1側)という。なお、図示していないが、カテーテル1は、ガイディングカテーテルに挿入された状態で使用され、ガイドワイヤ11(後述)と共に血管内の目的部位まで導かれる。
(Catheter 1)
As shown in FIG. 1, the catheter 1 includes a catheter body 10 and a hub 20.
The catheter 1 shown in FIG. 1 is used, for example, for imaging a thrombus formed in a cerebral blood vessel and for collecting a thrombus with a stent (described later). In the present specification, the side where the catheter body 10 is inserted into the blood vessel is referred to as the "tip side" (X2 side), and the front side (hub 20 side) where the practitioner operates the catheter 1 is referred to as the "base end side" (the proximal end side). X1 side). Although not shown, the catheter 1 is used while being inserted into the guiding catheter, and is guided to a target site in the blood vessel together with the guide wire 11 (described later).
 カテーテル本体10は、血管内に挿入される部分であり、全体が細長い筒状に形成されている。カテーテル本体10は、芯材となる螺旋状コイル、網目状の編組コイル等が樹脂層により被覆されており、全体として可撓性を有する。カテーテル本体10の外径は、例えば、0.55~2.1mmである。また、カテーテル本体10の内径は、例えば、0.33~1.78mmである。なお、図2等の断面図においては、上述した螺旋状コイル、樹脂層等の図示を省略している。図1に示すように、カテーテル本体10は、血管内に挿入される際に先端側となる領域に造影剤放出部100(後述)を備えている。 The catheter body 10 is a portion to be inserted into a blood vessel, and the entire catheter body 10 is formed in an elongated tubular shape. The catheter body 10 has a spiral coil as a core material, a mesh-like braided coil, and the like coated with a resin layer, and has flexibility as a whole. The outer diameter of the catheter body 10 is, for example, 0.55 to 2.1 mm. The inner diameter of the catheter body 10 is, for example, 0.33 to 1.78 mm. In the cross-sectional view of FIG. 2 and the like, the above-mentioned spiral coil, resin layer, and the like are not shown. As shown in FIG. 1, the catheter body 10 is provided with a contrast medium discharging portion 100 (described later) in a region on the distal end side when inserted into a blood vessel.
 ハブ20は、カテーテル本体10の基端側に設けられる部材である。ハブ20の内部は、カテーテル本体10と連通している。ハブ20は、カテーテル本体10に造影剤を注入したり、ステント(後述)を挿入したりする際の入口となる部分である。また、ハブ20は、施術者がカテーテル本体10等を操作する際に把持する部分でもある。 The hub 20 is a member provided on the proximal end side of the catheter body 10. The inside of the hub 20 communicates with the catheter body 10. The hub 20 is a portion that serves as an entrance when a contrast medium is injected into the catheter body 10 or a stent (described later) is inserted. The hub 20 is also a portion that the practitioner grips when operating the catheter body 10 and the like.
(造影剤放出部100)
 図2に示すように、本実施形態では、カテーテル本体10の先端側に設けられた範囲S1の部分が造影剤放出部100となる。範囲S1は、造影剤放出部100の中心軸方向Xにおいて、最も基端側(X1側)に設けられた放出孔110の基端側の端と、最も先端側(X2側)に設けられた放出孔110の先端側の端との間となる。
(Contrast agent release unit 100)
As shown in FIG. 2, in the present embodiment, the portion of the range S1 provided on the distal end side of the catheter main body 10 is the contrast medium discharging portion 100. The range S1 is provided at the distal end side end of the discharge hole 110 provided on the most proximal end side (X1 side) and on the most distal end side (X2 side) in the central axial direction X of the contrast medium discharge portion 100. It is between the end of the discharge hole 110 on the distal end side.
 造影剤放出部100の範囲S1の長さは、造影の対象となる血栓の長手方向の長さ等に応じて設定される。例えば、造影の対象となる血栓の長さが50mmと想定される場合、造影剤放出部100の範囲S1の長さは、80mm程度となる。血栓の造影を行う場合、想定される血栓の長さに適した造影剤放出部100を有するカテーテル1(カテーテル本体10)が選択される。想定される血栓の長さは、例えば、カテーテル1を挿入する血管の部位、内径、血流量等に基づいて、施術者により総合的に判断される。 The length of the range S1 of the contrast medium discharging portion 100 is set according to the length in the longitudinal direction of the thrombus to be imaged. For example, when the length of the thrombus to be imaged is assumed to be 50 mm, the length of the range S1 of the contrast medium discharging portion 100 is about 80 mm. When angiography of a thrombus is performed, a catheter 1 (catheter body 10) having a contrast medium discharging portion 100 suitable for the assumed length of the thrombus is selected. The assumed length of the thrombus is comprehensively determined by the practitioner based on, for example, the site of the blood vessel into which the catheter 1 is inserted, the inner diameter, the blood flow rate, and the like.
 本実施形態において、造影剤放出部100の外径及び内径は、カテーテル本体10と同じである。実施形態では、造影剤放出部100に設けられる放出孔110(後述)の個数、配置、直径等の一例を明記するが、これらは造影剤放出部100の外径、内径、範囲S1の長さ等に応じて適宜に選択される。 In the present embodiment, the outer diameter and inner diameter of the contrast medium discharging portion 100 are the same as those of the catheter main body 10. In the embodiment, an example of the number, arrangement, diameter, etc. of the discharge holes 110 (described later) provided in the contrast medium discharge unit 100 will be specified, but these are the outer diameter, inner diameter, and length of the range S1 of the contrast agent discharge unit 100. Etc., it is appropriately selected.
 図2に示すように、造影剤放出部100の側面には、造影剤放出部100の中心軸方向Xに沿って、複数(本例では、合計で18個)の放出孔110が設けられている。放出孔110は、カテーテル本体10に注入された造影剤を外部に放出する部分である。図2及び図3に示すように、第1実施形態の各放出孔110は、造影剤放出部100の中心軸方向Xと直交する方向に貫通している。 As shown in FIG. 2, a plurality of (18 in total in this example) discharge holes 110 are provided on the side surface of the contrast medium discharge unit 100 along the central axis direction X of the contrast medium discharge unit 100. There is. The discharge hole 110 is a portion that discharges the contrast medium injected into the catheter body 10 to the outside. As shown in FIGS. 2 and 3, each discharge hole 110 of the first embodiment penetrates in a direction orthogonal to the central axis direction X of the contrast medium discharge portion 100.
 カテーテル本体10において、造影剤放出部100よりも先端側(X2側)には、先端開口部101が設けられている。血栓の回収時において、ステント31(後述)は、先端開口部101から外部に押し出される。血栓の造影時において、カテーテル本体10に注入された造影剤は、造影剤放出部100の放出孔110だけでなく、先端開口部101からも放出される。カテーテル本体10において、先端開口部101と造影剤放出部100との間には、マーカー102が設けられている。マーカー102は、カテーテル本体10の遠位側の位置を確認するための目印となるリング状の部材である。マーカー102は、X線不透過性を有する金属材料により構成される。 In the catheter body 10, a tip opening 101 is provided on the tip side (X2 side) of the contrast medium discharging portion 100. At the time of collecting the thrombus, the stent 31 (described later) is pushed out from the tip opening 101. At the time of contrasting the thrombus, the contrast medium injected into the catheter body 10 is discharged not only from the discharge hole 110 of the contrast medium discharge portion 100 but also from the tip opening 101. In the catheter body 10, a marker 102 is provided between the tip opening 101 and the contrast medium discharging portion 100. The marker 102 is a ring-shaped member that serves as a mark for confirming the position of the catheter body 10 on the distal side. The marker 102 is made of a metal material having X-ray impermeable property.
 図2及び図3に示すように、複数の放出孔110は、造影剤放出部100の中心軸方向Xに沿って、造影剤放出部100のY(Y1-Y2)方向の側面及びZ(Z1-Z2)方向の側面に、それぞれ等間隔に設けられている。図3に示すように、造影剤放出部100のY(Y1-Y2)方向の側面に設けられる放出孔110と、造影剤放出部100のZ(Z1-Z2)方向の側面に設けられる放出孔110は、造影剤放出部100の中心軸方向Xにおいて、距離Lのピッチで等間隔に配置されている。距離Lは、例えば、1~80mmである。また、放出孔110の直径d(図2参照)は、例えば、0.2~0.6mmである。放出孔110は、例えば、カテーテル本体10において、造影剤放出部100となる領域にレーザ光を照射したり、穴開けポンチ等を突き刺したりすることにより形成できる。 As shown in FIGS. 2 and 3, the plurality of discharge holes 110 are formed on the side surface of the contrast agent discharge unit 100 in the Y (Y1-Y2) direction and Z (Z1) along the central axis direction X of the contrast agent discharge unit 100. The sides in the −Z2) direction are provided at equal intervals. As shown in FIG. 3, a discharge hole 110 provided on the side surface of the contrast medium discharge unit 100 in the Y (Y1-Y2) direction and a discharge hole provided on the side surface of the contrast medium discharge unit 100 in the Z (Z1-Z2) direction. The 110s are arranged at equal intervals at a pitch of a distance L in the central axis direction X of the contrast medium discharging unit 100. The distance L is, for example, 1 to 80 mm. The diameter d of the discharge hole 110 (see FIG. 2) is, for example, 0.2 to 0.6 mm. The discharge hole 110 can be formed, for example, by irradiating a region to be the contrast medium discharge portion 100 with a laser beam or piercing a hole punch or the like in the catheter main body 10.
 図2に示すように、造影剤放出部100のY(Y1-Y2)方向の側面には、造影剤放出部100の中心軸方向Xに沿って、それぞれ4個の放出孔110が設けられている。造影剤放出部100のY(Y1-Y2)方向の側面に設けられた放出孔110は、造影剤放出部100の中心軸方向Xにおいて、Z(Z1-Z2)方向の側面に設けられた放出孔110と交互に配置されている。 As shown in FIG. 2, four discharge holes 110 are provided on the side surfaces of the contrast medium discharge unit 100 in the Y (Y1-Y2) direction along the central axis direction X of the contrast medium discharge unit 100. There is. The discharge holes 110 provided on the side surface of the contrast medium discharge unit 100 in the Y (Y1-Y2) direction are the discharge holes provided on the side surface in the Z (Z1-Z2) direction in the central axis direction X of the contrast medium discharge unit 100. It is arranged alternately with the holes 110.
 また、造影剤放出部100のY(Y1-Y2)方向の側面に設けられた各放出孔110は、中心軸方向Xの各位置において、図4に示すように、造影剤放出部100の中心軸aを間に挟んで、径方向の対向する位置に設けられている。すなわち、造影剤放出部100のY(Y1-Y2)方向の側面に設けられた各放出孔110は、中心軸方向Xの各位置においてそれぞれ2箇所設けられると共に、造影剤放出部100の周方向CDに沿って180度の間隔で配置されている。言い換えると、造影剤放出部100のY(Y1-Y2)方向の側面において、各放出孔110は、造影剤放出部100の周方向CDに沿って等間隔に配置されている。 Further, each discharge hole 110 provided on the side surface of the contrast medium discharge unit 100 in the Y (Y1-Y2) direction is the center of the contrast medium discharge unit 100 at each position in the central axial direction X, as shown in FIG. It is provided at positions facing each other in the radial direction with the shaft a in between. That is, each discharge hole 110 provided on the side surface of the contrast medium discharge unit 100 in the Y (Y1-Y2) direction is provided at two locations at each position in the central axial direction X, and is provided in the circumferential direction of the contrast medium discharge unit 100. They are arranged at 180 degree intervals along the CD. In other words, on the side surface of the contrast medium discharging unit 100 in the Y (Y1-Y2) direction, the discharge holes 110 are arranged at equal intervals along the circumferential CD of the contrast medium discharging unit 100.
 図3に示すように、造影剤放出部100のZ(Z1-Z2)方向の側面には、造影剤放出部100の中心軸方向Xに沿って、それぞれ5個の放出孔110が設けられている。造影剤放出部100のZ(Z1-Z2)方向の側面に設けられた各放出孔110は、造影剤放出部100の中心軸方向Xにおいて、Y(Y1-Y2)方向の側面に設けられた放出孔110と交互に配置されている。 As shown in FIG. 3, five discharge holes 110 are provided on the side surfaces of the contrast medium discharge unit 100 in the Z (Z1-Z2) direction along the central axis direction X of the contrast medium discharge unit 100. There is. Each discharge hole 110 provided on the side surface of the contrast medium discharge unit 100 in the Z (Z1-Z2) direction is provided on the side surface in the Y (Y1-Y2) direction in the central axis direction X of the contrast medium discharge unit 100. It is arranged alternately with the discharge holes 110.
 また、造影剤放出部100のZ(Z1-Z2)方向の側面に設けられた各放出孔110は、中心軸方向Xの各位置において、図5に示すように、造影剤放出部100の中心軸aを間に挟んで、径方向の対向する位置に設けられている。すなわち、造影剤放出部100のZ(Z1-Z2)方向の側面の各放出孔110は、中心軸方向Xの各位置においてそれぞれ2箇所設けられると共に、造影剤放出部100の周方向CDに沿って180度の間隔で配置されている。言い換えると、造影剤放出部100のZ(Z1-Z2)方向の側面において、各放出孔110は、造影剤放出部100の周方向CDに沿って等間隔に配置されている。
 造影剤放出部100のY(Y1-Y2)方向の側面及びZ(Z1-Z2)方向の側面の各放出孔110は、図4及び図5に示すように、互いに直交する位置に設けられている。
Further, each discharge hole 110 provided on the side surface of the contrast medium discharge unit 100 in the Z (Z1-Z2) direction is the center of the contrast agent discharge unit 100 at each position in the central axial direction X, as shown in FIG. It is provided at positions facing each other in the radial direction with the shaft a in between. That is, each discharge hole 110 on the side surface of the contrast medium discharge unit 100 in the Z (Z1-Z2) direction is provided at two locations at each position in the central axial direction X, and is along the circumferential direction CD of the contrast medium discharge unit 100. They are arranged at intervals of 180 degrees. In other words, on the Z (Z1-Z2) direction side surfaces of the contrast medium discharge unit 100, the discharge holes 110 are arranged at equal intervals along the circumferential CD of the contrast medium discharge unit 100.
As shown in FIGS. 4 and 5, the discharge holes 110 on the side surface in the Y (Y1-Y2) direction and the side surface in the Z (Z1-Z2) direction of the contrast medium discharge unit 100 are provided at positions orthogonal to each other. There is.
(カテーテル・ステント・システム30)
 本実施形態のカテーテル1により血栓を造影する際の手順を説明する前に、造影後に血栓を回収するカテーテル・ステント・システム30の構成について説明する。
 図6は、カテーテル・ステント・システム30の概念図である。図6に示すように、カテーテル・ステント・システム30は、カテーテル本体10(カテーテル1)と、ステント31と、を備えている。カテーテル・ステント・システム30は、カテーテル1(図1参照)と、血栓の長さにより選択されたステント31とを組み合わせたシステムである。なお、図6では、カテーテル本体10の先端側(X2側)に設けられる造影剤放出部100の図示を省略している。
(Catheter Stent System 30)
Before explaining the procedure for imaging the thrombus with the catheter 1 of the present embodiment, the configuration of the catheter stent system 30 for collecting the thrombus after the imaging will be described.
FIG. 6 is a conceptual diagram of the catheter stent system 30. As shown in FIG. 6, the catheter stent system 30 includes a catheter body 10 (catheter 1) and a stent 31. The catheter stent system 30 is a system in which the catheter 1 (see FIG. 1) and the stent 31 selected according to the length of the thrombus are combined. In FIG. 6, the contrast medium discharging portion 100 provided on the distal end side (X2 side) of the catheter main body 10 is not shown.
 ステント31は、内部に血栓を収容可能なメッシュパターンを有する部材である。ステント31は、縮径された状態でカテーテル本体10内に挿入される。図6では、縮径されたステント31の断面を模式的に示している。ステント31の基端部32には、ワイヤ33が連結されている。ワイヤ33は、ステント31を血管内の目的部位へ押し出す際には先端側(X2側)へ送り込まれ、ステント31を体外へ取り出す際には基端側(X1側)へ引き出される。 The stent 31 is a member having a mesh pattern capable of accommodating a thrombus inside. The stent 31 is inserted into the catheter body 10 in a reduced diameter state. FIG. 6 schematically shows a cross section of the reduced diameter stent 31. A wire 33 is connected to the proximal end portion 32 of the stent 31. The wire 33 is sent to the distal end side (X2 side) when pushing the stent 31 to the target site in the blood vessel, and is pulled out to the proximal end side (X1 side) when the stent 31 is taken out of the body.
(血栓の造影)
 次に、第1実施形態のカテーテル1を用いて、血栓を造影する手順について説明する。図7A、図7B及び図7Cは、カテーテル1により血管内の血栓を造影する手順を示す模式図である。図7A~図7Cでは、放出孔110の位置を分かり易くするため、血栓BC内におけるガイドワイヤ11、造影剤放出部100を実線で示している。また、図7A~図7Cでは、血管BV内において、施術者に近い近位側をD1、施術者から離れた遠位側をD2として説明する。なお、血栓を造影する際には、以下の説明以外にも種々の作業が行われるが、ここでは説明を省略する。
(Thrombus contrast)
Next, a procedure for imaging a thrombus using the catheter 1 of the first embodiment will be described. 7A, 7B and 7C are schematic views showing a procedure for imaging a thrombus in a blood vessel with a catheter 1. In FIGS. 7A to 7C, the guide wire 11 and the contrast medium discharge portion 100 in the thrombus BC are shown by solid lines in order to make the position of the discharge hole 110 easy to understand. Further, in FIGS. 7A to 7C, the proximal side close to the practitioner is referred to as D1 and the distal side away from the practitioner is referred to as D2 in the blood vessel BV. In addition to the following description, various operations are performed when contrasting the thrombus, but the description will be omitted here.
 まず、図7Aに示すように、患者の血管BV内にガイドワイヤ11を挿入し、遠位側D2に送り込み、病変部位となる血栓BCの内部を貫通させて、血栓BCの遠位側に到達させる。なお、ガイドワイヤ11は、血栓BCを貫通していなくてもよく、例えば、血栓BCと血管BVの内表面との間に通過させてもよい。また、血栓BCの位置は、事前に頭部CT、MRI検査、脳血管造影等を行うことにより、大まかに特定することができる。ガイドワイヤ11が血栓BCの内部を貫通したか否かは、ガイディングカテーテル又はマイクロカテーテルから造影剤を注入して行う血管造影や、事前の検査により得られた情報等に基づいて判断される。 First, as shown in FIG. 7A, the guide wire 11 is inserted into the patient's blood vessel BV, sent to the distal side D2, penetrates the inside of the thrombus BC which is the lesion site, and reaches the distal side of the thrombus BC. Let me. The guide wire 11 does not have to penetrate the thrombus BC, and may be passed between the thrombus BC and the inner surface of the blood vessel BV, for example. In addition, the position of thrombus BC can be roughly identified by performing head CT, MRI examination, cerebral angiography, etc. in advance. Whether or not the guide wire 11 has penetrated the inside of the thrombus BC is determined based on angiography performed by injecting a contrast medium from a guiding catheter or a microcatheter, information obtained by a preliminary examination, and the like.
 次に、図7Bに示すように、ガイドワイヤ11に外挿させるようにして、カテーテル本体10を近位側D1から遠位側D2に送り込み、カテーテル本体10の先端を血栓BCの遠位側D2に到達させる。続いて、カテーテル本体10からガイドワイヤ11を引き抜く。 Next, as shown in FIG. 7B, the catheter body 10 is sent from the proximal side D1 to the distal side D2 so as to be extrapolated to the guide wire 11, and the tip of the catheter body 10 is inserted into the distal side D2 of the thrombus BC. To reach. Subsequently, the guide wire 11 is pulled out from the catheter body 10.
 次に、カテーテル本体10の基端側から造影剤を注入する。これにより、図7Cに示すように、造影剤放出部100の各放出孔110及び先端開口部101から造影剤(図中、小矢印)が放出される。放出された造影剤は、血栓BCの近位側D1及び遠位側D2に拡散し、その近傍に滞留する。図7Cにおいて、符号CA1は、血栓BCの近位側D1に滞留した造影剤による造影領域を示している。符号CA2は、血栓BCの遠位側D2に滞留した造影剤による造影領域を示している。X線透過の画像において、造影領域CA1及びCA2は、血管内の他の部分(例えば、血栓BC)とは明度が異なるため、施術者は、X線透過の画像に写った造影領域CA1及びCA2を視認することにより、血栓BCの近位側D1及び遠位側D2の位置を確認できる。施術者は、X線透過の画像において、血栓BCの近位側D1及び遠位側D2の位置を確認した時点で造影剤の注入を停止する。 Next, the contrast medium is injected from the proximal end side of the catheter body 10. As a result, as shown in FIG. 7C, the contrast medium (small arrow in the figure) is discharged from each discharge hole 110 and the tip opening 101 of the contrast medium discharge unit 100. The released contrast medium diffuses to the proximal side D1 and the distal side D2 of the thrombus BC and stays in the vicinity thereof. In FIG. 7C, reference numeral CA1 indicates a contrast region due to the contrast agent retained in D1 on the proximal side of thrombus BC. Reference numeral CA2 indicates a contrast-enhanced region due to the contrast medium retained in D2 on the distal side of thrombus BC. In the X-ray transmission image, the contrast areas CA1 and CA2 have different brightness from other parts in the blood vessel (for example, thrombus BC), so that the practitioner can see the contrast areas CA1 and CA2 in the X-ray transmission image. The positions of the proximal side D1 and the distal side D2 of the thrombus BC can be confirmed by visually recognizing. The practitioner stops the injection of the contrast medium when the positions of the proximal side D1 and the distal side D2 of the thrombus BC are confirmed in the X-ray transmission image.
 以上の作業により、施術者は、X線透過の画像において、血栓BCの近位側D1の位置と遠位側D2の位置を、それぞれ造影領域CA1及びCA2により確認できる。したがって、施術者は、X線透過の画像において、造影領域CA1とCA2との間を測定することにより、血栓BCの長さを、より正確に把握できる。この後、施術者は、血栓BCの長さに応じたステント31を選択し、血栓BCの回収を行う。 Through the above work, the practitioner can confirm the positions of the proximal side D1 and the distal side D2 of the thrombus BC in the contrast-enhanced areas CA1 and CA2, respectively, in the X-ray transmission image. Therefore, the practitioner can more accurately grasp the length of the thrombus BC by measuring the distance between the contrast-enhanced regions CA1 and CA2 in the X-ray transmission image. After this, the practitioner selects the stent 31 according to the length of the thrombus BC and collects the thrombus BC.
(血栓の回収)
 次に、カテーテル・ステント・システム30(図6参照)を操作して血栓を回収する手順について説明する。
 図8A、図8B、図8C及び図8Dは、カテーテル・ステント・システム30により血管内の血栓を回収する手順を示す模式図である。ここでは、血栓BCの造影を行った後、続けて血栓の回収を行う例について説明する。なお、図8A~図8Dでは、造影剤放出部100(放出孔110)の符号等を省略する。
(Recovery of blood clots)
Next, the procedure for operating the catheter stent system 30 (see FIG. 6) to collect the thrombus will be described.
8A, 8B, 8C and 8D are schematic views showing the procedure for collecting a thrombus in a blood vessel by the catheter stent system 30. Here, an example in which thrombus BC is imaged and then thrombus is collected will be described. In FIGS. 8A to 8D, the reference numerals of the contrast medium discharge unit 100 (release hole 110) and the like are omitted.
 まず、図8Aに示すように、ステント31を縮径した状態でカテーテル本体10内に挿入し、ワイヤ33を操作して、血栓BCの遠位側D2に送り込む。そして、ステント31の先端を、血栓BCよりも遠位側D2に位置させる。 First, as shown in FIG. 8A, the stent 31 is inserted into the catheter body 10 in a reduced diameter state, and the wire 33 is operated to send the stent 31 to the distal side D2 of the thrombus BC. Then, the tip of the stent 31 is positioned on the distal side D2 of the thrombus BC.
 次に、図8Bに示すように、血栓BCの位置でカテーテル本体10の先端からステント31を押し出して展開させる。具体的には、カテーテル本体10を図8Aに示す位置から近位側D1に引き込むことにより、ステント31は、相対的にカテーテル本体10から押し出されて展開する。ステント31は、その全体がカテーテル本体10から押し出される。 Next, as shown in FIG. 8B, the stent 31 is pushed out from the tip of the catheter body 10 at the position of the thrombus BC and deployed. Specifically, by pulling the catheter body 10 from the position shown in FIG. 8A into the proximal side D1, the stent 31 is relatively pushed out from the catheter body 10 and deployed. The entire stent 31 is extruded from the catheter body 10.
 次に、図8Cに示すように、ワイヤ33と共にカテーテル本体10を近位側D1へ引き込む。これにより、図8Dに示すように、血栓BCを捕捉したステント31を体外に引き出すことができる。
 以上の手順でカテーテル・ステント・システム30を操作することにより、血管BV内から血栓BCを体外に回収できる。
Next, as shown in FIG. 8C, the catheter body 10 is pulled into the proximal side D1 together with the wire 33. As a result, as shown in FIG. 8D, the stent 31 that has captured the thrombus BC can be pulled out of the body.
By operating the catheter stent system 30 in the above procedure, the thrombus BC can be recovered from the inside of the blood vessel BV to the outside of the body.
 上述した第1実施形態のカテーテル1によれば、カテーテル本体10の先端部から造影剤を放出させる場合に比べて、血栓BCの遠位側D2に、より多くの造影剤を拡散させることができる。そのため、施術者は、X線透過の画像において、血栓BCの近位側D1の位置と遠位側D2の位置を造影領域CA1及びCA2により確認できる。したがって、施術者は、X線透過の画像により、血栓BCの長さを、より正確に把握できる。また、施術者が血栓BCの長さに適した必要最小限の長さのステント31を選択することにより、血栓を捕捉したステント31を体外に引き出した際、より長いステントを選択した比べて、ステント31が血管壁に引っ掛かりにくくなるため、血管壁への負担を軽減できる。 According to the catheter 1 of the first embodiment described above, a larger amount of the contrast medium can be diffused to the distal side D2 of the thrombus BC as compared with the case where the contrast medium is discharged from the tip end portion of the catheter body 10. .. Therefore, the practitioner can confirm the position of the proximal side D1 and the position of the distal side D2 of the thrombus BC by the contrast regions CA1 and CA2 in the X-ray transmission image. Therefore, the practitioner can more accurately grasp the length of the thrombus BC from the X-ray transmission image. In addition, when the practitioner selects a stent 31 having the minimum necessary length suitable for the length of the thrombus BC, when the stent 31 that has captured the thrombus is pulled out of the body, a longer stent is selected as compared with the case where the stent 31 is selected. Since the stent 31 is less likely to be caught on the blood vessel wall, the burden on the blood vessel wall can be reduced.
 第1実施形態の造影剤放出部100において、放出孔110は、造影剤放出部100の中心軸方向Xに沿って等間隔に設けられている。これによれば、造影剤放出部100の中心軸方向Xにおいて造影剤が均等に放出されるため、X線透過の画像において、血栓BCの長さを、より正確に把握できる。例えば、血栓BCの長さが想定よりも短い場合でも、造影剤放出部100の中心軸方向Xにおいて造影剤が均等に放出されることにより、血栓BCの遠位側D2の位置に、より多くの造影剤を拡散させることができる。 In the contrast medium discharge unit 100 of the first embodiment, the discharge holes 110 are provided at equal intervals along the central axis direction X of the contrast medium discharge unit 100. According to this, since the contrast medium is evenly discharged in the central axis direction X of the contrast medium discharge unit 100, the length of the thrombus BC can be grasped more accurately in the X-ray transmission image. For example, even if the length of the thrombus BC is shorter than expected, the contrast medium is evenly released in the central axis direction X of the contrast medium discharging portion 100, so that the contrast medium BC is more located at the position of the distal side D2 of the thrombus BC. Contrast medium can be diffused.
 第1実施形態の造影剤放出部100において、放出孔110は、造影剤放出部100の周方向CDに沿って等間隔に配置されている。そのため、造影剤放出部100の周方向CDにおいて、造影剤をより均等に放出させることができる。 In the contrast medium discharge unit 100 of the first embodiment, the discharge holes 110 are arranged at equal intervals along the circumferential CD of the contrast medium discharge unit 100. Therefore, the contrast medium can be discharged more evenly in the circumferential CD of the contrast medium discharge unit 100.
 第1実施形態の造影剤放出部100において、放出孔110は、造影剤放出部100の径方向の対向する位置に設けられている。そのため、各放出孔110から造影剤を放出させた際の反動により、造影剤放出部100が中心軸aと直交する方向にずれてしまうことを抑制できる。 In the contrast medium discharge unit 100 of the first embodiment, the discharge holes 110 are provided at positions facing each other in the radial direction of the contrast medium discharge unit 100. Therefore, it is possible to prevent the contrast medium discharge portion 100 from being displaced in the direction orthogonal to the central axis a due to the reaction when the contrast medium is discharged from each discharge hole 110.
[第2実施形態]
 第2実施形態の造影剤放出部100は、側面に設けられる放出孔110の貫通方向が第1実施形態と異なる。そのため、後述する図9では、造影剤放出部100(カテーテル本体10)のみを図示し、カテーテル1の全体の図示を省略する。また、第2実施形態の説明及び図面において、第1実施形態と同等の部材等には、第1実施形態と同一の符号を付し、重複する説明を省略する。
[Second Embodiment]
The contrast medium discharging unit 100 of the second embodiment has a different penetrating direction of the discharge holes 110 provided on the side surface from that of the first embodiment. Therefore, in FIG. 9, which will be described later, only the contrast medium discharging portion 100 (catheter body 10) is shown, and the entire catheter 1 is not shown. Further, in the description and drawings of the second embodiment, members and the like equivalent to those of the first embodiment are designated by the same reference numerals as those of the first embodiment, and duplicate description will be omitted.
 図9は、第2実施形態の造影剤放出部100の構成を示す図である。図9は、第1実施形態の図2に相当する図である。図9では、造影剤放出部100のZ(Z1-Z2)方向の側面に設けられた放出孔110のみを図示している。また、図9に示すX-Z方向は、図2に準じている。 FIG. 9 is a diagram showing the configuration of the contrast medium discharging unit 100 of the second embodiment. FIG. 9 is a diagram corresponding to FIG. 2 of the first embodiment. In FIG. 9, only the discharge hole 110 provided on the side surface of the contrast medium discharge unit 100 in the Z (Z1-Z2) direction is shown. The XX directions shown in FIG. 9 are based on FIG. 2.
 図9に示すように、第2実施形態の造影剤放出部100は、各放出孔110の内側の開口OP1が造影剤放出部100先端側(X2側)に位置し、外側の開口OP2が造影剤放出部100の後端側(X1側)に位置するように、中心軸方向Xと斜めに交差する方向に貫通している。各放出孔110の中心軸bが造影剤放出部100の中心軸aと交差する角度αは、例えば、30°~90°未満である。 As shown in FIG. 9, in the contrast medium discharging portion 100 of the second embodiment, the opening OP1 inside each of the discharging holes 110 is located on the tip side (X2 side) of the contrast medium discharging portion 100, and the outer opening OP2 is contrasted. It penetrates in a direction diagonally intersecting the central axis direction X so as to be located on the rear end side (X1 side) of the agent discharging portion 100. The angle α at which the central axis b of each discharge hole 110 intersects the central axis a of the contrast medium discharge portion 100 is, for example, 30 ° to less than 90 °.
 第2実施形態の造影剤放出部100を備えたカテーテル本体10によれば、縮径した状態でカテーテル本体10内に挿入されたステント31(図6参照)を、造影剤放出部100の先端側(X2側)に押し出した際、ステント31が放出孔110の開口OP1に引っ掛かりにくくなる。そのため、造影剤放出部100の先端開口部101からステント31を、よりスムーズに展開させることができる。 According to the catheter body 10 provided with the contrast medium discharging unit 100 of the second embodiment, the stent 31 (see FIG. 6) inserted into the catheter body 10 in a reduced diameter state is placed on the distal end side of the contrast medium discharging unit 100. When extruded to (X2 side), the stent 31 is less likely to be caught in the opening OP1 of the discharge hole 110. Therefore, the stent 31 can be more smoothly deployed from the tip opening 101 of the contrast agent discharging portion 100.
 第2実施形態の造影剤放出部100において、各放出孔110の中心軸bと造影剤放出部100の中心軸aと交差する角度αは、すべて同じであってもよいし、放出孔110の位置に応じて異なっていてもよい。また、第2実施形態の造影剤放出部100において、第1実施形態の放出孔110のように、中心軸bと造影剤放出部100の中心軸aと交差する角度αが90°となる放出孔110が含まれていてもよい。 In the contrast medium discharging portion 100 of the second embodiment, the angle α at which the central axis b of each discharging hole 110 and the central axis a of the contrast medium discharging portion 100 intersect may be the same, or the angle α of the discharging hole 110 may be the same. It may be different depending on the position. Further, in the contrast medium discharge unit 100 of the second embodiment, the angle α at which the central axis b intersects with the central axis a of the contrast medium discharge unit 100 is 90 °, as in the discharge hole 110 of the first embodiment. The hole 110 may be included.
 以上、本発明の実施形態について説明したが、本発明は、前述した第1及び第2実施形態(以下、総称して「実施形態」ともいう)に限定されるものではなく、後述する変形形態のように種々の変形や変更が可能であって、それらも本開示の技術的範囲内に含まれる。また、実施形態に記載した効果は、本開示から生じる最も好適な効果を列挙したに過ぎず、実施形態に記載したものに限定されない。なお、上述の実施形態及び後述する変形形態は、適宜に組み合わせて用いることもできるが、詳細な説明は省略する。 Although the embodiments of the present invention have been described above, the present invention is not limited to the first and second embodiments described above (hereinafter, also collectively referred to as “embodiments”), and the modified embodiments described later. Various modifications and changes are possible, such as, which are also included within the technical scope of the present disclosure. In addition, the effects described in the embodiments are merely a list of the most suitable effects resulting from the present disclosure, and are not limited to those described in the embodiments. The above-described embodiment and the modified form described later can be used in combination as appropriate, but detailed description thereof will be omitted.
(変形形態)
 図10は、造影剤放出部100の変形例を示す断面図である。図10は、例えば、第1実施形態の図4又は図5の断面図に相当する。
 図10に示すように、変形形態の造影剤放出部100において、放出孔110は、造影剤放出部100の側面において、互いに120°離れた位置に設けられている。すなわち、図10に示す造影剤放出部100の放出孔110は、中心軸方向Xの各位置において3箇所設けられると共に、造影剤放出部100の周方向CDに沿って120度の間隔で設けられている。
 なお、造影剤放出部100の放出孔110は、中心軸方向Xの各位置において4又はそれ以上設けられていてもよいし、中心軸方向Xの各位置において異なる数の放出孔110が設けられていてもよい。
(Transformed form)
FIG. 10 is a cross-sectional view showing a modified example of the contrast medium discharging portion 100. FIG. 10 corresponds to, for example, a cross-sectional view of FIG. 4 or FIG. 5 of the first embodiment.
As shown in FIG. 10, in the modified contrast medium discharging portion 100, the discharging holes 110 are provided at positions 120 ° apart from each other on the side surface of the contrast medium discharging portion 100. That is, the discharge holes 110 of the contrast medium discharge unit 100 shown in FIG. 10 are provided at three locations at each position in the central axial direction X, and are provided at intervals of 120 degrees along the circumferential CD of the contrast medium discharge unit 100. ing.
The discharge holes 110 of the contrast medium discharge unit 100 may be provided with 4 or more at each position in the central axial direction X, or different numbers of discharge holes 110 are provided at each position in the central axial direction X. You may be.
 図11A及び図11Bは、造影剤放出部100の変形例を示す側面図である。図11A及び図11Bは、例えば、第1実施形態の図2に示す側面図に相当する。
 図11Aに示す造影剤放出部100は、放出孔110が中心軸方向Xに沿って異なるピッチで設けられている。具体的には、造影剤放出部100の中心軸方向Xに沿って6箇所設けられた放出孔110のうち、後端側(X1側)及び先端側(X2側)に設けられた2つの放出孔110a及び110bは、距離L1のピッチで配置されている。放出孔110bとこれに隣接する放出孔110cは、距離L2(>L1)のピッチで配置されている。放出孔110cとこれに隣接する放出孔110dは、距離L3(>L2)のピッチで配置されている。なお、放出孔110が設けられる側面は、造影剤放出部100のY方向又はZ方向のいずれでもよい。
11A and 11B are side views showing a modified example of the contrast medium discharging portion 100. 11A and 11B correspond to, for example, the side views shown in FIG. 2 of the first embodiment.
In the contrast medium discharge unit 100 shown in FIG. 11A, the discharge holes 110 are provided at different pitches along the central axis direction X. Specifically, of the six discharge holes 110 provided along the central axis direction X of the contrast medium discharge portion 100, two discharge holes provided on the rear end side (X1 side) and the front end side (X2 side). The holes 110a and 110b are arranged at a pitch of a distance L1. The discharge holes 110b and the discharge holes 110c adjacent thereto are arranged at a pitch of a distance L2 (> L1). The discharge holes 110c and the discharge holes 110d adjacent thereto are arranged at a pitch of a distance L3 (> L2). The side surface on which the discharge hole 110 is provided may be in either the Y direction or the Z direction of the contrast medium discharge portion 100.
 図11Aに示す造影剤放出部100は、中心軸方向Xの両端側では放出孔110が密に配置され、中央付近では放出孔110が疎に配置されている。すなわち、本形態の造影剤放出部100は、想定される長さの血栓BCに貫通させた場合に、血栓BCの近位側(D1側)及び遠位側(D2側)に位置すると考えられる放出孔110a及び110bのピッチを短くし、血栓BCの中間付近に位置すると考えられる放出孔110c及び110dのピッチを長くしている。 In the contrast medium discharge portion 100 shown in FIG. 11A, the discharge holes 110 are densely arranged on both ends in the central axial direction X, and the discharge holes 110 are sparsely arranged near the center. That is, it is considered that the contrast medium releasing portion 100 of the present embodiment is located on the proximal side (D1 side) and the distal side (D2 side) of the thrombus BC when it is penetrated through the thrombus BC of the assumed length. The pitches of the discharge holes 110a and 110b are shortened, and the pitches of the discharge holes 110c and 110d, which are considered to be located near the middle of the thrombus BC, are lengthened.
 本形態の造影剤放出部100によれば、造影剤放出部100を血栓BCに貫通させた場合に、血栓BCの外側に位置すると考えられる放出孔は、短いピッチで配置されているため、造影剤を、血栓BCの近位側(D1)と遠位側(D2)に、より多く到達させることができる。また、本形態の造影剤放出部100によれば、造影剤放出部100を血栓BCに貫通させた場合に、血栓BCの中間付近に位置すると考えられる放出孔は、より長いピッチで配置されているため、造影に関与しない造影剤の放出量を低減できる。なお、図11Aでは、造影剤放出部100の側面の6箇所に放出孔110を設けた例について説明したが。本形態において、放出孔110を設ける位置は、5箇所以下でもよいし、7箇所以上でもよい。 According to the contrast medium discharge unit 100 of the present embodiment, when the contrast medium discharge unit 100 is penetrated through the thrombus BC, the discharge holes that are considered to be located outside the thrombus BC are arranged at a short pitch, so that the contrast medium is imaged. More agent can be delivered to the proximal side (D1) and the distal side (D2) of thrombus BC. Further, according to the contrast medium discharge unit 100 of the present embodiment, when the contrast medium discharge unit 100 is penetrated through the thrombus BC, the discharge holes considered to be located near the middle of the thrombus BC are arranged at a longer pitch. Therefore, the amount of contrast medium released that is not involved in contrast can be reduced. In addition, in FIG. 11A, an example in which discharge holes 110 are provided at six locations on the side surface of the contrast medium discharge portion 100 has been described. In the present embodiment, the positions where the discharge holes 110 are provided may be 5 or less, or 7 or more.
 図11Bに示す造影剤放出部100は、中心軸方向Xの両端側の1箇所に、それぞれ放出孔110e及び110fが設けられている。すなわち、本形態の造影剤放出部100は、想定される長さの血栓BCに貫通させた場合に、血栓BCの近位側(D1側)に位置する放出孔110aと、遠位側(D2側)に位置する放出孔110bのみを備えている。例えば、想定される血栓BCの長さを50mmとした場合、本形態の造影剤放出部100の放出孔110aと110bとの間隔(又は図2の範囲S1)は、80mm程度となる。 The contrast medium discharge unit 100 shown in FIG. 11B is provided with discharge holes 110e and 110f at one location on both ends in the central axial direction X, respectively. That is, the contrast medium discharge unit 100 of the present embodiment has a discharge hole 110a located on the proximal side (D1 side) of the thrombus BC and a distal side (D2) when the thrombus BC of the assumed length is penetrated. It has only a discharge hole 110b located on the side). For example, when the assumed length of the thrombus BC is 50 mm, the distance between the discharge holes 110a and 110b of the contrast medium discharge unit 100 of the present embodiment (or the range S1 in FIG. 2) is about 80 mm.
 本形態の造影剤放出部100においても、造影剤放出部100を血栓BCに貫通させた場合に、造影剤を、血栓BCの近位側(D1)と遠位側(D2)に、より多く到達させることができる。また、本形態の造影剤放出部100によれば、造影剤放出部100を血栓BCに貫通させた場合に、血栓BCの中間付近になると考えられる位置には放出孔が設けられていないため、造影に関与しない造影剤の放出量をより一層低減できる。 Also in the contrast medium releasing section 100 of the present embodiment, when the contrast medium releasing section 100 is penetrated through the thrombus BC, more contrast medium is applied to the proximal side (D1) and the distal side (D2) of the thrombus BC. Can be reached. Further, according to the contrast medium discharging unit 100 of the present embodiment, when the contrast medium discharging unit 100 is penetrated through the thrombus BC, a discharge hole is not provided at a position considered to be near the middle of the thrombus BC. The amount of contrast medium released that is not involved in contrast can be further reduced.
 実施形態では、カテーテル本体10の先端側となる領域の一部を、造影剤放出部100として構成した例について説明した。これに限らず、カテーテル本体10とは別体の造影剤放出部100を、カテーテル本体10の先端に取り付けてもよい。 In the embodiment, an example in which a part of the region on the distal end side of the catheter body 10 is configured as the contrast medium discharging portion 100 has been described. Not limited to this, a contrast medium discharging portion 100 separate from the catheter main body 10 may be attached to the tip of the catheter main body 10.
 実施形態では、図8A~図8Dに示すように、造影剤放出部100から造影剤を放出させた後、同じカテーテル本体10にステント31を挿入する例について説明した。これに限らず、造影剤放出部100から造影剤を放出させた後、カテーテル本体10を体外に引き出し、縮径したステント31を挿入した別のカテーテル本体10を挿入してもよい。その場合、造影用のカテーテル本体10の造影剤放出部100は、先端側(X2側)を封止した構成とすることができる。造影剤放出部100の先端側を封止することにより、造影剤放出部100の側面に設けた放出孔110から、より多くの造影剤を放出させることができる。 In the embodiment, as shown in FIGS. 8A to 8D, an example in which the stent 31 is inserted into the same catheter body 10 after the contrast medium is discharged from the contrast medium discharge unit 100 has been described. Not limited to this, after the contrast medium is discharged from the contrast medium discharge unit 100, the catheter body 10 may be pulled out of the body and another catheter body 10 into which the reduced-diameter stent 31 is inserted may be inserted. In that case, the contrast medium discharging portion 100 of the catheter body 10 for contrast medium may have a configuration in which the distal end side (X2 side) is sealed. By sealing the tip end side of the contrast medium discharging section 100, a larger amount of contrast medium can be discharged from the discharging holes 110 provided on the side surface of the contrast medium discharging section 100.
 1 カテーテル
 10 カテーテル本体
 100 造影剤放出部
 110 放出孔
1 Catheter 10 Catheter body 100 Contrast medium discharge part 110 Release hole

Claims (6)

  1.  筒状のカテーテル本体を備えるカテーテルであって、
     前記カテーテル本体は、血管内へ挿入される際に先端側となる領域に設けられた造影剤放出部と、前記造影剤放出部の側面に設けられた複数の放出孔と、を備え、
     前記放出孔は、前記造影剤放出部の中心軸方向の両端部に、少なくとも1つずつ設けられているカテーテル。
    A catheter with a tubular catheter body
    The catheter body includes a contrast medium discharge portion provided in a region on the distal end side when inserted into a blood vessel, and a plurality of discharge holes provided on the side surface of the contrast medium discharge portion.
    A catheter provided with at least one discharge hole at both ends in the central axis direction of the contrast agent discharge portion.
  2.  複数の前記放出孔は、前記造影剤放出部の中心軸方向に沿って等間隔に設けられている、請求項1に記載のカテーテル。 The catheter according to claim 1, wherein the plurality of discharge holes are provided at equal intervals along the central axis direction of the contrast medium discharge portion.
  3.  複数の前記放出孔は、前記造影剤放出部の周方向に沿って等間隔に設けられている、請求項1又は2に記載のカテーテル。 The catheter according to claim 1 or 2, wherein the plurality of discharge holes are provided at equal intervals along the circumferential direction of the contrast medium discharge portion.
  4.  複数の前記放出孔は、前記造影剤放出部の径方向の対向する位置に設けられている、請求項1~3のいずれかに記載のカテーテル。 The catheter according to any one of claims 1 to 3, wherein the plurality of discharge holes are provided at positions facing each other in the radial direction of the contrast medium discharge portion.
  5.  複数の前記放出孔の少なくとも1つは、前記造影剤放出部の中心軸方向と直交する方向に貫通している、請求項1~4のいずれかに記載のカテーテル。 The catheter according to any one of claims 1 to 4, wherein at least one of the plurality of discharge holes penetrates in a direction orthogonal to the central axis direction of the contrast medium discharge portion.
  6.  複数の前記放出孔の少なくとも1つは、内側の開口が前記造影剤放出部の先端側に位置し、外側の開口が前記造影剤放出部の後端側に位置するように、前記造影剤放出部の中心軸方向と斜めに交差する方向に貫通している、請求項1~4のいずれかに記載のカテーテル。 At least one of the plurality of discharge holes releases the contrast medium so that the inner opening is located on the distal end side of the contrast medium discharge portion and the outer opening is located on the rear end side of the contrast medium discharge portion. The catheter according to any one of claims 1 to 4, which penetrates in a direction obliquely intersecting the central axis direction of the portion.
PCT/JP2020/021738 2020-04-17 2020-06-02 Catheter WO2021210188A1 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
JP2020074008A JP2021168846A (en) 2020-04-17 2020-04-17 catheter
JP2020-074008 2020-04-17

Publications (1)

Publication Number Publication Date
WO2021210188A1 true WO2021210188A1 (en) 2021-10-21

Family

ID=78083867

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/JP2020/021738 WO2021210188A1 (en) 2020-04-17 2020-06-02 Catheter

Country Status (2)

Country Link
JP (1) JP2021168846A (en)
WO (1) WO2021210188A1 (en)

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH11332990A (en) * 1998-05-28 1999-12-07 Terumo Corp Catheter
US6063069A (en) * 1997-05-19 2000-05-16 Micro Therapeutics Inc. Method and apparatus for power lysis of a thrombus
JP2003520080A (en) * 2000-01-07 2003-07-02 アシスト メディカル システムズ, インコーポレイテッド Anti-recoil catheter
JP2004215689A (en) * 2003-01-09 2004-08-05 Jiima Kk Catheter for angiography

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6063069A (en) * 1997-05-19 2000-05-16 Micro Therapeutics Inc. Method and apparatus for power lysis of a thrombus
JPH11332990A (en) * 1998-05-28 1999-12-07 Terumo Corp Catheter
JP2003520080A (en) * 2000-01-07 2003-07-02 アシスト メディカル システムズ, インコーポレイテッド Anti-recoil catheter
JP2004215689A (en) * 2003-01-09 2004-08-05 Jiima Kk Catheter for angiography

Also Published As

Publication number Publication date
JP2021168846A (en) 2021-10-28

Similar Documents

Publication Publication Date Title
CN104161548B (en) A kind of utensil and application thereof for the treatment of arterial occlusion pathological changes
JP4234994B2 (en) Guided transluminal intervention using vessel wall penetration catheters and other devices
AU2014281178B2 (en) Access needles and stylet assemblies
US20190209047A1 (en) Devices, systems and methods for enhanced visualization of the anatomy of a patient
JP5778585B2 (en) Method, system and apparatus for transjugular intrahepatic portal generalization shunting
JPH02241446A (en) Positioning needle assembly for focus
JP5506105B2 (en) catheter
DE112013001181T5 (en) Access device for lung nodes and method of use
JP7256245B2 (en) Recanalization catheter system
CN113456189A (en) Puncture system
CN216876523U (en) Puncture instrument
CN216876522U (en) Puncture instrument
CN113456191A (en) Puncture instrument
CN113456190A (en) Puncture instrument
CN113520549A (en) Puncture instrument
CN211884905U (en) Balloon dilatation catheter and balloon thereof
WO2021210188A1 (en) Catheter
CN216754558U (en) Puncture system
JP2024500098A (en) Medical catheter and its manufacturing method
JP4315770B2 (en) Body cavity diagnosis system
JP4624019B2 (en) catheter
JP2008504865A (en) Markers for positioning in living tissue
JP6824609B2 (en) Angioplasty guide wire navigation
JP2018191883A (en) Medical long body
CN204072153U (en) A kind of utensil for the treatment of arterial occlusion pathological changes

Legal Events

Date Code Title Description
121 Ep: the epo has been informed by wipo that ep was designated in this application

Ref document number: 20930658

Country of ref document: EP

Kind code of ref document: A1

NENP Non-entry into the national phase

Ref country code: DE

122 Ep: pct application non-entry in european phase

Ref document number: 20930658

Country of ref document: EP

Kind code of ref document: A1