JP5945586B2 - Medical device guide system - Google Patents

Description

  The present invention relates to a medical device guide system.

  2. Description of the Related Art Conventionally, an endoscope that can be arranged with an observation window and a channel opening facing each other is known (for example, see Patent Document 1). According to such an endoscope, the treatment tool that has been moved in and out of the channel is photographed from the front side. That is, in the endoscopic image, the surgical site can be easily and accurately treated with the treatment tool without the surgical part and the distal end of the treatment tool being hidden behind the shadow of the outer jacket of the treatment tool.

Japanese Patent No. 3432893

  However, in the pericardial space between the heart and the pericardium that encloses the heart, a complicated operation of the endoscope is required as compared with the case of a lumen that only needs to be operated in the front-rear direction. That is, in the case of the endoscope of Patent Document 1, for example, when only the endoscope is rotated in the circumferential direction, the treatment tool is also rotated together. There is a problem that it is difficult to operate each of them in a desired position and posture.

  The present invention has been made in view of the above-described circumstances, and allows an endoscope and a treatment tool to be placed in desired positions and postures while the state of treatment by the treatment tool can be easily observed by an endoscopic image. It is an object of the present invention to provide a medical device guide system that can be easily operated.

In order to achieve the above object, the present invention provides the following means.
A reference example of the present invention provides an endoscope including an elongated insertion portion that can be inserted into a pericardial cavity, and a guide wire that is fixed to the insertion portion and extends forward from the distal end of the insertion portion.
According to the reference example of the present invention, the endoscope can be guided into the pericardial cavity by following the guide wire by inserting the guide wire through the pericardium and inserting it into the pericardial cavity. . In addition, by inserting the treatment instrument from the distal end side of the guide wire along the guide wire, the distal end of the treatment instrument is arranged to face the distal end of the insertion portion. Easy to observe.

  In this case, since the endoscope and the treatment instrument can be operated independently in the front-rear direction and the circumferential direction, both of them can be easily operated to a desired position and posture. Further, the channel for inserting the guide wire into the insertion portion is not necessary, and the insertion portion can be reduced in diameter.

In the reference example of the above invention, it is preferable that the insertion portion has a gradually decreasing diameter at the distal end portion toward the distal end.
By doing in this way, the insertion part can be easily penetrated into the pericardium while gradually expanding the perforation of the pericardium through which the guide wire has penetrated.

  Further, the reference example of the present invention can be inserted into the pericardial cavity, and an elongated tube member in which a lumen into which the treatment instrument is inserted is formed in the longitudinal direction, and is fixed to the tube member, and the distal end of the tube member And a guide wire extending forward from the guide device.

  According to the reference example of the present invention, the tube member can be guided into the pericardial cavity by following the guide wire by penetrating the pericardium and inserting it into the pericardial cavity. Further, by inserting the insertion portion of the endoscope from the distal end side of the guide wire along the guide wire, the distal end of the insertion portion is arranged to face the distal end of the treatment instrument. The state of treatment can be easily observed. Moreover, since the endoscope and the treatment tool can be operated independently in the front-rear direction and the circumferential direction, both of them can be easily operated to a desired position and posture. Further, the guide member lumen is not required for the tube member, and the tube member can be reduced in diameter.

Moreover, the reference example of this invention provides a guide wire provided with the branch wire branched in the middle position of the longitudinal direction.
According to the reference example of the present invention, the position where the branch wire is branched is arranged in the pericardial cavity, and the insertion portion of the endoscope and the treatment tool are inserted from both ends and the end of the branch wire, respectively. It is possible to place three or more endoscopes and the distal end of the treatment tool so as to face each other in the pericardial cavity. In addition, the endoscope and the treatment tool can be easily arranged at desired positions and postures, respectively.

  In addition, a reference example of the present invention is a guide wire that guides an insertion portion provided in an endoscope and a tube member provided in a guide device in a pericardial cavity, and is a convex curve curved at a predetermined curvature at an intermediate position in the longitudinal direction. Provided is a guide wire that is brazed in shape and has lower flexibility than the insertion portion or the tube member.

  According to the reference example of the present invention, the convex part is disposed in the pericardial cavity, and the insertion part of the endoscope and the tube member of the guide device are respectively inserted into the pericardial cavity from each end, thereby Since the distal end and the distal end of the tube member are opposed to each other, the state of treatment by the treatment instrument inserted into the pericardial cavity via the tube member can be easily observed with an endoscope. In addition, the endoscope and the treatment tool can be easily operated to desired positions and postures, respectively. Further, by disposing the distal end of the insertion portion or the distal end of the tube member on the convex portion, these distal ends can be disposed at an angle with respect to the heart surface.

  A reference example of the present invention is a guide wire for guiding an insertion portion provided in an endoscope and a tube member provided in a guide device in a pericardial cavity, and is folded back into a substantially U shape at an intermediate position in the longitudinal direction. A first curved portion that is brazed into a curved shape, and a second curved portion that is brazed into a shape in which one side of the first curved portion is curved at a predetermined angle with respect to the other side. The first bending portion and the second bending portion provide a guide wire having lower flexibility than the insertion portion and the tube member.

  According to the reference example of the present invention, the first bending portion and the second bending portion are arranged in the pericardial cavity, and the insertion portion of the endoscope and the tube member of the guide device are respectively bent from both ends. Of the treatment with the treatment tool which is made to protrude from the distal end of the tube member by inserting the distal end portion or the second curved portion into the pericardial cavity so as to face each other at a predetermined angle. Can be easily observed with an endoscope. In addition, the endoscope and the treatment tool can be easily operated to desired positions and postures, respectively.

  In addition, a reference example of the present invention includes a flexible guide wire that can be bent in a substantially U shape in the pericardial cavity, and an elongated insertion portion in which a channel into which the guide wire is inserted is formed in the longitudinal direction. There is provided a medical device guide system comprising: an endoscope provided with the endoscope; and a medical device guide system including a movement restriction mechanism that restricts movement of the guide wire inserted into the channel toward a proximal end side.

  According to the reference example of the present invention, since the insertion portion and the treatment tool are respectively inserted from both ends of the guide wire inserted into the pericardial cavity, the insertion portion and the distal end of the treatment tool are opposed to each other in the pericardial cavity. The state of treatment with the treatment tool can be easily observed with the endoscope. In addition, the endoscope and the treatment tool can be easily operated to desired positions and postures, respectively. In this case, the movement restriction mechanism restricts the retraction of the guide wire in the channel, so that the guide wire can be prevented from being pulled out of the pericardial cavity due to pulsation.

In the reference example of the above invention, the movement restriction mechanism may include a fixing portion that is provided on the proximal end side of the channel and fixes a part of the proximal end side of the guide wire.
By doing in this way, the position of a guide wire can be easily fixed by the operator at hand.

Further, in the reference example of the invention, the movement restriction mechanism includes a plurality of recesses arranged along the longitudinal direction and recessed in the radial direction at one halfway position of the guide wire or the channel, and the guide wire or the A convex portion provided on the other side of the channel and engaged with the concave portion may be provided. Alternatively, the movement restriction mechanism may include a male screw portion provided at an intermediate position of the guide wire and a female screw portion provided in the channel and meshing with the male screw portion.
By doing in this way, the fine adjustment of the position of the insertion portion in the longitudinal direction with respect to the guide wire can be facilitated, and can be stably held at the finely adjusted position.

  In addition, the reference example of the present invention includes a flexible guide wire that can be bent into a substantially U shape in the pericardial cavity, a first lumen into which the guide wire is inserted, and a first guide in which the treatment instrument is inserted. Medical device comprising a guide device comprising an elongated tube member having two lumens formed in the longitudinal direction, and a movement restricting mechanism for restricting movement of the guide wire inserted into the first lumen to the proximal side Provide a device guidance system.

In the reference example of the above invention, the movement restriction mechanism may include a fixing portion that is provided on a proximal end side of the first lumen and fixes a part of the proximal end side of the guide wire.
Further, in the reference example of the above invention, the movement restricting mechanism is arranged along the longitudinal direction at one halfway position of the guide wire or the lumen and recessed in the radial direction, and the guide wire or the lumen. A convex portion that is provided and engages with the concave portion may be provided. Alternatively, the movement restriction mechanism may include a male screw portion provided at an intermediate position of the guide wire and a female screw portion provided in the lumen and meshing with the male screw portion.

  In addition, the reference example of the present invention includes a flexible guide wire that can be bent into a substantially U shape in the pericardial cavity, a first lumen into which the guide wire is inserted, and a first guide in which the treatment instrument is inserted. And a guide device having a flexible elongated tube member formed in the longitudinal direction, the first lumen being disposed at intervals in the longitudinal direction, and the penetrating portion into which the guide wire is inserted The medical device guide system is provided with a stopper having an outer diameter larger than the hole diameter of the penetrating portion at a midway position in the longitudinal direction.

  According to the reference example of the present invention, since the insertion portion and the treatment tool are respectively inserted from both ends of the guide wire inserted into the pericardial cavity, the insertion portion and the distal end of the treatment tool are opposed to each other in the pericardial cavity. The state of treatment with the treatment tool can be easily observed with the endoscope. In addition, the endoscope and the treatment tool can be easily operated to desired positions and postures, respectively. In this case, the tube member can be curved at the portion where the guide wire is exposed from within the first channel by applying a compressive force in the longitudinal direction to the tube member by abutting the tip of the tube member against the stopper.

  The present invention also provides a flexible guide wire that can be bent in a substantially U shape in the pericardial cavity, and a channel that can be inserted into the pericardial cavity, and the guide wire is inserted in the longitudinal direction. An endoscope having an elongated insertion portion formed in the longitudinal direction, a first lumen that can be inserted into the pericardial cavity, and into which the guide wire is inserted and a second lumen into which the treatment instrument is inserted A guide device comprising an elongated tube member formed in the guide wire, wherein the guide wire is provided at an intermediate position in the longitudinal direction at an interval according to the depth of field of the endoscope, the channel and the channel Provided is a medical device guide system having two stoppers having an outer diameter larger than the diameter of an opening on each distal end side of a first lumen.

  According to the present invention, the insertion portion and the treatment tool are respectively inserted from both ends of the guide wire inserted into the pericardial cavity so that the insertion portion and the distal end of the treatment tool are opposed to each other in the pericardial space. The state of treatment with the treatment tool can be easily observed with the mirror. In addition, the endoscope and the treatment tool can be easily operated to desired positions and postures, respectively. In this case, by inserting the insertion portion and the tube member to a position where they abut against the stopper, the insertion portion and the tube member are placed at a position where the endoscopic image is focused on the treatment tool protruded from the tip of the tube member. Can be arranged.

  According to the present invention, it is possible to easily operate the endoscope and the treatment tool to a desired position and posture, respectively, while it is possible to easily observe the state of treatment by the treatment tool using the endoscope image. Play.

1 is an overall configuration diagram of a medical device guide system according to an embodiment of the present invention. It is a figure which shows an example of a structure of the fixing | fixed part of FIG. 1, (a) The state which has released the guide wire, and (b) The state which has fixed the guide wire. It is a figure explaining operation | movement of the curved part formed in the front-end | tip part of the guide apparatus of FIG. 1, (a) The state extended | stretched on the substantially straight line, and (b) The curved state, respectively are shown. It is a figure which shows the stopper provided in the guide wire of FIG. It is a figure explaining the positional relationship of the endoscope inserted to the position of the stopper of FIG. 4, and a guide apparatus. It is a figure explaining the relationship between the position of the affected part of a heart, and the curve shape of a guide wire. It is a figure explaining another relationship between the position of the affected part of a heart, and the curve shape of a guide wire. It is a figure explaining the sheath insertion step and guide wire insertion step of the medical device guide method using the medical device guide system of FIG. It is a figure explaining the acquisition step of the medical device guide method by the medical device guide system of FIG. It is a figure explaining the extraction step of the medical device guide method which carried out the medical device guide system of FIG. It is a figure explaining the opposing step of the medical device guide method which carried out the medical device guide system of FIG. (A) The figure which shows the state which one of the insertion part or the tube fitted in the groove | channel of the heart surface, (b) It is a figure explaining the method for making one pull out from a groove | channel by operating the other. It is a figure explaining the method of arrange | positioning the guide wire in which the magnet was provided in the middle position in the pericardial space in the substantially U shape. It is a figure explaining the method of arrange | positioning a guide wire in a pericardial cavity in a substantially U shape using one sheath. It is a figure which shows the structure of the modification of the endoscope provided with the guide wire at the front-end | tip. It is a figure which shows the structure of another modification of the endoscope provided with the guide wire at the front-end | tip. FIG. 16 is a diagram illustrating an example of a configuration in which a guide wire is detachably provided at a distal end of an insertion portion in the endoscope of FIG. 15. (A) The figure which shows the modification of the guide wire which has a loop-shaped convex part, (b) It is a figure explaining the usage method of the guide wire of (a). (A) The figure which shows the modification of the guide wire which has a semicircle-shaped convex part, (b) It is a figure explaining the usage method of the guide wire of (a). It is a figure which shows another modification of the guide wire which has a semicircle-shaped convex part. It is a figure which shows an example of a structure of a cancellation | release mechanism. It is a figure explaining the effect | action of the cancellation | release mechanism of FIG. 21, (a) The state which the convex part is engaging with the dentition, and (b) The state where the convex part was disengaged from the dentition are shown. Yes. It is a figure which shows the modification of a guide wire provided with the 1st bending part and the 2nd bending part. It is a figure explaining the usage method of the guide wire of FIG. It is a figure explaining another usage method of the guide wire of FIG. It is a figure explaining the usage method of a guide wire provided with a branch wire.

Hereinafter, an endoscope 1, a guide device 10, a guide wire 20, a medical device guide system 100 including these, and a medical device guide using the medical device guide system 100 according to an embodiment of the present invention. The method will be described with reference to the drawings.
As shown in FIG. 1, a medical device guide system 100 according to this embodiment includes an endoscope 1, a guide device 10 that guides a treatment instrument 30, and a guide that guides the endoscope 1 and the guide device 10. A wire 20 and two cylindrical sheaths 40 into which the endoscope 1 and the guide device 10 are respectively inserted are provided.

  The endoscope 1 is a direct-view type for observing the visual field F in the front direction, and has an elongated insertion portion 2 that can be inserted into the pericardial cavity A, and a guide wire 20 that is formed so as to penetrate along the longitudinal direction of the insertion portion 2. Is inserted, and an observation window 4 provided on the distal end surface of the insertion portion 2 is provided. The endoscope 1 images external light collected through the observation window 4 with an optical system (not shown). Information on the captured image is displayed on a monitor (not shown) via the cable 5.

  On the proximal end side of the channel 3 of the endoscope 1, a fixing portion (movement restriction mechanism) 50 that fixes the position of the guide wire 20 is provided. For example, as shown in FIG. 2 (a), the fixing portion 50 communicates with the inside of the channel 3 and is gradually tapered toward the inside of the channel 3. The fixing portion 50 is inserted into the opening 51 and is substantially inserted. A rubber plug 53 having a hole 52 formed in the center thereof and a cap 54 fixed to the rubber plug 53 are provided. The cap 54 is attached to the opening 51 by a screw mechanism (not shown). When the operator rotates the cap 54 in the closing direction with the guide wire 20 inserted into the hole 52, the rubber plug 53 is inserted into the opening 51, and as shown in FIG. The guide wire 20 is fastened by the inner surface of the hole 52 that is recessed.

  The guide device 10 includes an elongated tube (tube member) 11 that can be inserted into the pericardial cavity A. The tube 11 has a first lumen 12 and a second lumen 13 formed so as to penetrate along the longitudinal direction. A guide wire 20 is inserted into the first lumen 12, and a treatment tool 30 is inserted into the second lumen 13.

  As shown in FIG. 3A, the tube 11 has a groove 14 formed on a side surface at a part of the distal end side. Thereby, the first lumen 12 is formed up to a middle position on the distal end side, and a part of the guide wire 20 is exposed to the outside of the tube 11. That is, the part in which the groove 14 is formed has higher flexibility than the other part. Moreover, the tube 11 has the penetration part 15 by which the guide wire 20 is penetrated by the front-end | tip.

  As a result, as shown in FIG. 3B, the tube 11 is further pushed in a state where the distal end surface of the tube 11 is abutted against a first stopper (described later) 21, or the guide wire 20 is pulled to make the longitudinal direction By applying this compressive force to the tube 11, the portion where the groove 14 is formed is easily curved. That is, the curved portion 16 is constituted by the portion where the groove 14 is formed. In the state where the bending portion 16 is bent in this way, the treatment tool 30 is caused to appear and disappear from the first lumen 12 in an oblique direction with respect to the longitudinal direction of the tube 11. Therefore, the treatment tool 30 can easily perform treatment even at a relatively deep position from the surface of the heart B. For example, when a syringe is used as the treatment tool 30, a drug can be injected at a relatively deep position from the surface of the heart B.

  As shown in FIG. 4, the guide wire 20 includes a first stopper 21 and a second stopper 22 that are disposed at intermediate positions at intervals in the longitudinal direction. The first stopper 21 has an outer diameter larger than the inner diameter of the channel 3, and the second stopper 22 has an outer diameter larger than the inner diameter of the through portion 15 of the tube 11. The distance between the first stopper 21 and the second stopper 22 is such that the endoscope 1 is in focus so that the treatment instrument 30 projected and retracted from the second lumen 13 is in focus. It is determined according to the depth of field.

  As a result, the insertion portion 2 and the tube 11 inserted from each end of the guide wire 20 to the position where they hit the stoppers 21 and 22 along the guide wire 20 have an appropriate observation distance as shown in FIG. It will be distributed in the sky. In this state, the observation window 4 and the illumination window (not shown) provided on the distal end surface of the insertion portion 2 and the opening of the second lumen 13 of the tube 11 are not covered by the stoppers 21 and 22. The outer diameters of the first stopper 21 and the second stopper 22 are respectively designed.

  Further, the guide wire 20 is brazed in advance in a substantially U shape in the middle in the longitudinal direction according to the position of the affected part of the heart B. For example, when the affected part C exists on the front wall of the heart B, as shown in FIG. 6, the guide wire 20 is bent into a substantially U shape curved with a relatively large curvature so that the guide wire 20 is folded in the middle of the front wall. Attached. On the other hand, when the affected part C is present on the posterior wall of the heart B, as shown in FIG. 7, the guide wire 20 is curved with a relatively small curvature so that the guide wire 20 is turned around the outside of the heart B. It is brazed into a U shape.

Thereby, when the operator inserts the guide wire 20 into the pericardial cavity A, the guide wire 20 can be easily arranged along a desired route. In addition, the position of the affected part C can be easily selected simply by changing the curved shape of the guide wire 20 to be worn.
At least part of the guide wire 20 may be made of a shape memory alloy so that the crimped shape of the guide wire 20 is more accurately reproduced in the pericardial cavity A.

  Further, the guide wire 20 has flexibility lower than that of the insertion portion 2 and the tube 11 at least in a brazed portion. Thereby, when the insertion part 2 and the tube 11 are inserted along the guide wire 20, the guide wire 20 is bent and the shape is not changed, and the insertion part 2 and the tube 11 are secured by the guide wire 20. You can guide along the route exactly. 6 and 7, the stoppers 21 and 22 are not shown.

Next, a medical device guide method using the medical device guide system 100 configured as described above will be described with reference to FIGS.
In the medical device guide method according to the present embodiment, the U-shaped forming step S1 in which the guide wire 20 is arranged in a substantially U shape in the pericardial cavity A, and the insertion portion 2 and the tube 11 are placed along the guide wire 20 in the heart. An endoscope insertion step S2 and a guide device insertion step S3 that are respectively inserted into the membrane cavity A, and an opposing step S4 in which the distal end of the insertion portion 2 and the distal end of the tube 11 are arranged to face each other are provided.

In the U-shaped formation step S1, the guide wire 20 and the grasping tool 60 are inserted into the pericardial cavity A through the two sheaths 40 inserted into the pericardial cavity A from the body surface D of the patient, and X-ray This is performed by operating the guide wire 20 and the gripping tool 60 while observing with a fluoroscopic image.
Specifically, first, the sheath 40 is inserted into the body from under the xiphoid process, and is inserted into the pericardial cavity A through the different positions of the pericardium E in the vicinity of the apex (sheath insertion step).

  Next, as shown in FIG. 8, the guide wire 20 is inserted into the pericardial cavity A through the inside of one sheath 40 and the grasping tool 60 is inserted into the pericardial cavity A through the inside of the other sheath 40 (guide wire insertion step). ). The grasping tool 60 may be any device that can easily grasp the guide wire 20. For example, forceps, a snare, and a basket are preferably used. Next, as shown in FIG. 9, the distal end portion of the guide wire 20 is gripped by the gripping tool 60 (capturing step). Next, the gripping tool 60 is pulled out of the body through the other sheath 40 while the guidewire 20 is gripped (pulling step).

  By the above procedure, as shown in FIG. 10, the guide wire 20 is disposed outside the body at both ends, and the intermediate position is brazed in the pericardial cavity A in advance and disposed in a substantially U shape. Next, the insertion portion 2 and the tube 11 are inserted into the pericardial cavity A from each end of the guide wire 20 through the sheath 40, and the insertion portion 2 and the tube 11 are inserted into the first or second stoppers 21 and 22. It arrange | positions in the position which strikes (opposing step). As a result, as shown in FIG. 11, the observation window 4 provided on the distal end surface of the insertion portion 2 and the distal end surface of the tube 11 are substantially aligned with an appropriate observation distance.

  While the insertion portion 2 or the tube 11 is running along the guide wire 20, one of the insertion portion 2 or the tube 11 is fitted in the groove G on the surface of the heart B as shown in FIG. The other is operated laterally with respect to the insertion direction. As a result, as shown in FIG. 12B, one is pulled sideways through the guide wire 20, and the other can be easily pulled out of the groove G.

  The operator inserts the treatment tool 30 into the pericardial cavity A through the second lumen 13 of the tube 11 while observing the endoscopic image displayed on the monitor. At this time, the operator observes the treatment tool 30 that appears and disappears from the second lumen 13 from the front side. That is, in the endoscopic image, the distal end portion of the treatment tool 30 and the affected part C are not covered by the outer sheath of the treatment tool 30. Therefore, the operator can accurately perform the treatment while easily observing the state of treatment of the affected area C by the treatment tool 30 with the endoscopic image.

  In this case, the insertion part 2 and the treatment tool 30 can be operated independently from each other in the front-rear direction and the circumferential direction. Therefore, for example, the operator adjusts the posture and the front-rear direction position of the treatment tool 30 while fixing the field of view of the endoscopic image to the affected part C, or holds the insertion part 2 while holding the position of the treatment tool 30. It is possible to change the field of view by moving it. Thus, there exists an advantage that the insertion part 2 and the treatment tool 30 can each be easily operated to a desired position and attitude | position. Further, by using separate sheaths 40 for the insertion portion 2 and the tube 11, a thin one can be used as each sheath 40. That is, since each perforation formed in the pericardium E is small, these perforations can be easily closed after the operation, and the burden on the patient can be reduced.

  In addition, the method of arrange | positioning the guide wire 20 demonstrated in this embodiment in the substantially U shape in the pericardial cavity A is an example, and you may use another method.

  FIG. 13 is a diagram for explaining a method of using another guide wire 201 instead of the gripping tool 60. The guide wires 20 and 201 have magnets 23a and 23b that generate a magnetic attractive force to each other at an intermediate position. Each of the guide wires 20 and 201 is folded back at an intermediate position, and the folded portion is inserted into the sheath 40 with the folded portion at the top. In the pericardial cavity A, the guide wire 20 is captured by another guide wire 201 by the magnetic attraction of the magnets 23a and 23b. Then, the other guide wire 201 is pulled out of the body through the inside of the sheath 40, whereby the guide wire 20 is arranged in a substantially U shape in the pericardial cavity A.

  In this way, the guide wire 20 can be found and captured relatively easily in the pericardial cavity A. Further, in the pericardial cavity A, it is difficult to operate the guide wire 20 to the side, but it can be easily performed to the side by pushing and pulling the ends of the looped guide wires 20 and 201. In addition, the guide wires 20 and 201 can be operated.

  FIG. 14 is a diagram for explaining a method of using one sheath 40. In this method, a sheath 40 having an inner diameter capable of simultaneously inserting both the insertion portion 2 and the tube 11 is used. In this case, the guide wire 20 is folded at an intermediate position, and inserted into the sheath 40 with the folded position as the head, so that it is not necessary to search for and supplement the guide wire 20 in the pericardial cavity A, and the operation is simple. The guide wire 20 can be arranged in a substantially U shape.

  As another example, another endoscope having a channel for the gripper may be used instead of the gripper 60. For example, after inserting another endoscope into the pericardial cavity A and finding the guide wire by the endoscopic image, the gripper is inserted into the pericardial cavity A through the channel and the guide wire is inserted. Capture and pull one end of the gripper and guidewire out of the body through the channel. By operating while observing with an endoscopic image in this way, the operation is easier and more reliable than when operating the guide wire 20 and the gripping tool 60 while confirming the positions of the fluoroscopic image. can do.

  Further, a sheath 40 having a curved distal end may be used as the sheath 40 so that the guide wire 20 can be projected and retracted in a desired direction in the pericardial cavity A. In this case, by arranging two sheaths with curved tip portions so that the tip surfaces face each other in the pericardial cavity, the guide wire protruded from one sheath can be easily guided into the other sheath. And can be pulled out of the body.

  In the present embodiment, as the endoscope 1, as shown in FIG. 15 or FIG. 16, a guide wire 20 fixed to the distal end of the insertion portion 2 may be used. In this way, when the guide wire 20 is inserted into the sheath 40 and the pericardial cavity A, the insertion portion 2 is also inserted following the guide wire 20. That is, since the guide wire channel 3 is not required, the insertion portion 2 can be reduced in diameter. Further, after the guide wire 20 is arranged in a substantially U shape in the pericardial cavity A and one end is pulled out of the body, the insertion portion 2 can be easily operated by pushing and pulling the one end.

  In this case, the distal end portion of the insertion portion 2 has a conical shape whose diameter gradually decreases toward the distal end so that the insertion portion 2 can easily penetrate the small perforation of the pericardium E through which the guide wire 20 penetrates. It is formed. For example, as shown in FIG. 15, a conical cap 6 made of an optically transparent member such as glass may be provided at the tip.

  Alternatively, as shown in FIG. 16, the tip surface may be formed obliquely, and a conical optical member 8 may be provided in front of the illumination window 7. Reference numeral 9 denotes an optical fiber that guides the illumination light L from a light source (not shown) disposed outside the body. In this case, in order to efficiently illuminate the region on the observation window 4 side, the surface of the optical member 8 opposite to the observation window 4 is preferably a mirror that reflects the illumination light L. The optical member 8 may include a light diffusing agent such as silica particles so as to uniformly diffuse the illumination light L reflected by the mirror.

  By configuring the distal end portion of the insertion portion 2 as shown in FIG. 15 or FIG. 16, the optical path between the field of view F, the observation window 4 and the illumination window 7 is increased without increasing the diameter of the distal end portion. Can be secured.

  The guide wire 20 shown in FIGS. 15 and 16 may be detachably provided at the distal end of the insertion portion 2. By doing in this way, the guide wire 20 can be easily exchanged, for example, with a different specification such as rigidity, length, outer diameter, etc., and the guide wire 20 suitable for the content of the operation can be used. It becomes possible.

  As a configuration in which the guide wire 20 is detachably attached to the distal end of the insertion portion 2, for example, as shown in FIGS. 17A and 17B, a female screw 9a is provided at the distal end portion of the cap 6, and a male screw is provided. A guide wire 20 is movably inserted into a through hole formed along the central axis of 9b. The female screw 9a has a diameter that decreases toward the base end.

  The male screw 9b is made of a flexible material and is provided with a cut in the longitudinal direction in a part of the circumferential direction, so that opposed side surfaces are parallel to each other in a normal state (FIG. 17 ( a), and the opposite side surfaces are close to each other by engaging with the female screw 9a (see FIG. 17B). By engaging the male screw 9b with the female screw 9a with the guide wire 20 inserted into the through hole, the guide wire 20 is fastened to the cap 6 by the inner surface of the male screw 9b. .

  The guide wire 20 may be fixed to the tip of the tube 11 instead of the insertion portion 2. In this case, since the tube 11 is inserted into the pericardial cavity A following the guide wire 20, the first lumen 12 is not required, and the tube 11 can be reduced in diameter.

In the present embodiment, the guide wire 20 is exemplified as having the two stoppers 21 and 22. However, instead of this, a convex portion formed by curving into a convex shape with a predetermined curvature at an intermediate position is provided. You may have. The convex part 24 may have a loop shape as shown in FIG. 18 (a), or may have a substantially semicircular shape as shown in FIG. 19 (a).
By doing in this way, the front-end | tip part of the tube 11 leaves the space | interval between the heart B surface in the convex part 24, as shown in FIG.18 (b) and FIG.19 (b). And are arranged at an angle. That is, even with the tube 11 that does not include the bending portion 16, a treatment can be performed on a relatively deep position from the surface of the heart B.

  In the configuration provided with the convex portion 24, as shown in FIG. 19A, the convex portion 24 is provided with a male screw portion (movement limiting mechanism) 25, and the second lumen 13 has a male screw portion 25 and When engaged, a female screw portion (not shown, movement restriction mechanism) may be provided. By doing in this way, the position and the angle with respect to the surface of the heart B can be easily finely adjusted by rotating the tube 11 in the circumferential direction. Further, the position of the tube 11 can be stably maintained regardless of the pulsation.

  Alternatively, instead of the male screw portion 25 and the female screw portion, as shown in FIG. 20, a ratchet mechanism, that is, a tooth row (movement restriction mechanism) 26 arranged in the longitudinal direction on the convex portion 24, and the second A convex portion (not shown, movement restriction mechanism) provided in the lumen 13 and engaged with a concave portion formed between adjacent teeth of the tooth row 26 may be provided. When the ratchet mechanism is provided, it is preferable that a release mechanism for releasing the restriction on the backward movement is provided.

  For example, as shown in FIG. 21, the release mechanism is configured by a catheter 70 that is accommodated in the second lumen 13 and that has a distal end portion that can expand radially outward by its elasticity. The distal end portion of the catheter 70 is composed of, for example, a plurality of (two in the illustrated example) sections 70a that are arranged in the circumferential direction and brazed in a shape that warps outward. The tip of the slice 70a is formed in a bowl shape to form a convex portion. As a result, the distal end portion of the catheter 70 becomes substantially straight in the second lumen 13 as shown in FIG. 22A, and the distal end of the section 70 a meshes with the concave portion of the tooth row 26. Then, the distal end portion of the catheter 70 is projected and retracted from within the second lumen 13, and as shown in FIG. 22 (b), is expanded in the radial direction and disposed at a position away from the dentition 26. As a result, the guide wire 20 is brought into a retreatable state.

  Further, as shown in FIG. 23, the guide wire 20 has a first curved portion 27a that is curved in a substantially U shape at a midway position, and one side of the first curved portion 27a is opposite to the other side. A second curved portion 27b that is curved at a predetermined angle and approximately 90 ° in the illustrated example may be provided. According to such a guide wire 20, the insertion portion 2 and the treatment instrument 30 are inserted by inserting the insertion portion 2 and the tube 11 to a position where they abut each other at the first bending portion 27a or the second bending portion 27b. They can be arranged at a predetermined angle. That is, such a guide wire 20 is used when the side view type having the observation window 4 on the side surface of the distal end portion is used as the endoscope 1 as shown in FIG. 24, or as shown in FIG. When the ablation catheter etc. in which the electrode 31 was provided in the side is used as the treatment tool 30, it is used suitably.

  Moreover, in this embodiment, although the case where one endoscope 1 and one guide device 10 were used was illustrated, as shown in FIG. 26, at least one branch wire 20a was provided in the middle position. Three or more endoscopes 1 and guide devices 10 may be used in combination using the guide wire 20. The branch wire 20a is configured by, for example, another wire connected to an intermediate position of one guide wire 20. By doing so, for example, even when two treatment tools are used simultaneously while observing with the endoscope 1, the state of treatment with each treatment tool can be easily observed from the substantially front side.

(Appendix)
In addition, the invention of the following structure is guide | induced from these embodiments.
(Additional item 1)
A U-shaped forming step in which a guide wire is disposed with its both ends positioned outside the pericardium and a midway position is curved in a substantially U shape within the pericardial cavity, and the heart is formed in the U-shaped forming step. An endoscope insertion step in which an endoscope is inserted into the pericardial cavity along the guide wire from one of the end portions arranged outside the membrane; and in the U-shaped formation step, on the outside of the pericardium A guide device insertion step of inserting a guide device into the pericardial cavity along the guide wire from the other end portion disposed, and the endoscope insertion step and the guide device insertion step in the pericardial cavity A medical device guide method comprising: an opposing step of disposing the endoscope and the distal end portions of the guide device that are inserted into each other so as to face each other at an intermediate position of the guide wire.

(Appendix 2)
The endoscope includes a guide wire extending forward from a distal end thereof, the U-shaped forming step is performed using the guide wire included in the endoscope, and the endoscope insertion step is performed using the U The medical device guide method according to claim 1, wherein the endoscope is inserted into the pericardial cavity following the guide wire inserted into the pericardial cavity in the character forming step.
(Additional Item 3)
The guide device includes a guide wire extending forward from a tip thereof, and the U-shaped forming step is performed using the guide wire included in the guide device, and the guide device inserting step is the U-shaped forming step. The medical device guide method according to claim 1, wherein the guide device is inserted into the pericardial cavity following the guide wire inserted into the pericardial cavity.

(Appendix 4)
The U-shaped forming step includes a sheath insertion step of inserting a cylindrical sheath from outside the body into the pericardial cavity, and a grasping tool capable of grasping the guide wire and the guide wire into the pericardial cavity through the sheath. A guide wire insertion step to be inserted; a capture step of capturing the guide wire by the gripper in the pericardial cavity; and the gripper together with the guidewire captured in the capture step through the sheath to the outside of the body The medical device guide method according to Item 1, further comprising a pulling-out step.

(Appendix 5)
The sheath insertion step inserts two sheaths into the pericardial cavity from different positions of the pericardium, and the guide wire insertion step passes the guide wire and the treatment instrument through different sheaths. The medical device guide method according to item 4, wherein the medical device is inserted.

(Appendix 6)
The guide wire insertion step includes a second magnet that generates a magnetic attractive force between the guide wire having the first magnet at a midway position and the first magnet at the midway position as the gripping tool. An additional guide wire, and the capturing step captures the guide wire with the second guide wire by magnetic attraction between the first magnet and the second magnet in the pericardial cavity Item 5. A medical device guide method according to Item 4.

(Appendix 7)
The medical device guide method according to claim 4, wherein the guide wire insertion step and the supplementary step are performed while observing the guide wire and the gripping tool with a fluoroscopic image.
(Appendix 8)
The step of inserting the guide wire inserts another endoscope into the pericardial cavity, inserts the gripper into the pericardial cavity via a channel of the other endoscope, and The medical device guide method according to claim 4, wherein the step is performed while observing the guide wire and the gripping tool with an endoscopic image captured by the other endoscope.

(Appendix 9)
In the U-shaped forming step, two sheaths with curved distal ends are inserted into the pericardial cavity so that the distal end surfaces thereof face each other, and the sheath insertion step inserts the sheath into the pericardial cavity. And a guide wire insertion step of inserting the guide wire into the pericardial cavity through the other sheath and then pulling the guide wire out of the body through the other sheath. Device guide method for.

DESCRIPTION OF SYMBOLS 1 Endoscope 2 Insertion part 3 Channel 4 Observation window 5 Cable 6 Cap 7 Illumination window 8 Optical member 9a Male screw 9b Female screw 10 Guide apparatus 11 Tube (tube member)
12 first lumen 13 second lumen 14 groove 15 penetrating portion 16 bending portion 20, 201 guide wire 20a branch wire 21 first stopper 22 second stopper 23a, 23b magnet 24 convex portion 25 male screw portion (movement restriction) mechanism)
26 dentition (movement restriction mechanism)
27a 1st bending part 27b 2nd bending part 30 treatment tool 31 electrode 40 sheath 50 fixing | fixed part (movement restriction mechanism)
51 opening 52 hole 53 rubber stopper 54 cap 60 gripper 100 medical device guide system A pericardial cavity B heart C affected area D body surface E pericardium F visual field G groove

Claims (4)

A flexible guide wire that can be bent into a substantially U shape in the pericardial cavity;
An endoscope comprising an elongated insertion portion that is insertable into the pericardial cavity and in which a channel into which the guide wire is inserted is formed in a longitudinal direction;
A guide device comprising an elongated tube member which is insertable into the pericardial cavity and in which a first lumen into which the guide wire is inserted and a second lumen into which a treatment instrument is inserted is formed in the longitudinal direction. ,
The guide wire is provided at an intermediate position in the longitudinal direction with an interval corresponding to the depth of field of the endoscope, and is larger than the aperture of each channel and the opening on the distal end side of the first lumen A medical device guide system having two stoppers having an outer diameter.   The medical device guide system according to claim 1, further comprising a movement restriction mechanism that restricts movement of the guide wire inserted into the channel toward a proximal end side.   The medical device guide system according to claim 2, wherein the movement restriction mechanism is provided on a proximal end side of the channel, and includes a fixing portion that fixes a part of the proximal end side of the guide wire. The first lumen is formed from the distal end of the tube member to a position spaced from the proximal end,
At the tip of the tube member,
A groove formed on a side surface at a distal end side of the first lumen and exposing a part of the guide wire protruding from the first lumen;
4. The device according to claim 1, further comprising a penetrating portion that is provided on a distal end side of the first lumen with the groove interposed therebetween and through which the guide wire penetrates in the longitudinal direction . Medical device guide system.

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