JP2011025054A - Intravascular stapler - Google Patents

Abstract

<P>PROBLEM TO BE SOLVED: To provide an intravascular stapler capable of stopping movement maybe happened in an artificial blood vessel, and capable of removing the risk of the movement in the future. <P>SOLUTION: This intravascular stapler for fixing the insertion type artificial blood vessel 264 to the blood vessel includes a staple housing 214 adapted to store at least one staple thereinto. The staple housing 214 includes an exit area 258 for discharge the at least one staple, an actuator 306 adapted to discharge the staple through the exit area 158, and a displacement mechanism operated combinedly with the staple housing in the vicinity of the exit area. The exit area 258 is pressed toward the inserion type artificial blood, when discharging the staple. The displacement mechanism is positioned in the vicinity of the exit area 258, and may include a balloon constituted to be expanded and contracted. The staples is formed into an extended W shape, and is bent when discharged. <P>COPYRIGHT: (C)2011,JPO&INPIT

Description

The present invention relates to a stapling instrument used for fixing an intravascular artificial blood vessel to a blood vessel wall.

Artificial vessel fixation utilizing the present invention may be performed during the initial implantation. However, the present invention can also be used to prevent such an annoying situation of proximal or distal movement of such an artificial blood vessel after initial implantation.

It is well known that endovascular artificial blood vessels can be inserted into a human body during various medical procedures. Typically, an artificial blood vessel is inserted into the blood vessel and held in place by friction such as a self-expandable or balloon expandable stent. The artificial blood vessel can also be secured to the blood vessel by hooks or barbs.

Artificial blood vessels are formed from polyester, expanded polytetrafluoroethylene (ePTFE) or other synthetic materials. Artificial blood vessels can also be formed from other regions of the body, or natural blood vessels taken from a donor mammal. Regardless of the various materials used, the movement of the artificial blood vessel over time becomes a problem.

Movement of the caudal instrument is known to result in type I endoleak with aneurysm sac reperfusion, hypertrophy and rupture. Movement of the cranial instrument can cover the renal artery ostium and develop renal failure.

Such movement of the instrument is caused by many factors. One known factor is poor patient choice. Patients with conical aortic neck, severe neck flexion, short neck, or laminating thrombus at the installation site are prone to instrument movement problems. Other instrument movement problems arise from changes in the aortic morphology after instrument implantation. Finally, migration can also be caused by structural fatigue of the instrument and problems associated with the instrument design. Even without these problems, instrument movement has been found.

The process of caudal movement has traditionally been done by adding a “sleeve” to the proximal end of the prosthesis, with the aim of regaining a foothold between the prosthesis and the blood vessel it attaches to seal between the two. Was done. More drastic options include appealing to normal surgery. Unfortunately, these recent methods are associated with high mortality rates.

Treatment options for head movement are less attractive. If moving continuously, abandoning is the only option because such movement results in renal failure requiring hemodialysis. Typical methods for removing the instrument include an celiac artery cross clamp,
There is a problem with that.

Previous attempts to secure moving equipment, including the installation of hooks, barbs, tackers and other fastening equipment, have proven inadequate or impractical. Therefore, it would be advantageous to use an intravascular stapling device that is used to secure new artificial blood vessels so as to properly stop possible movement and exclude the possibility of future movement. By actually fixing the artificial blood vessel to the aortic neck at multiple points, hypertrophy of the aorta itself is also prevented.

The endovascular stapler of the present invention is designed to overcome the disadvantages of the prior art. In certain embodiments, the endovascular stapler is adapted to receive at least one staple therein, and has a staple housing having an exit region for discharging at least one staple, and at least through the exit region. An activation assembly adapted to eject a single staple and a displacement mechanism that operates in conjunction with the staple housing near the exit region, wherein the displacement member is disposed in the exit region when ejecting at least one staple. Can be operated to press against the interstitial artificial blood vessel. The displacement mechanism may include a balloon located in the exit area. The balloon can be configured to selectively inflate and deflate. The balloon may be inelastic. The staples may be deformed before exiting the exit area. The stapler is also suitable for use with staples having an elongated W shape. Further, the activation assembly can include a pusher and a trigger, and the pusher can be configured to advance with a trigger to release at least one staple.

In another embodiment, an endovascular stapler for securing an interstitial artificial blood vessel to a blood vessel has a trigger housing that includes a trigger mechanism within the housing, a proximal end, and a distal end, the proximal A staple housing coupled with a trigger housing at an end and suitable for receiving staples and having a staple exit region formed therein near its distal end and an exterior of the staple housing near the distal end of the staple housing And a balloon configured to selectively inflate and deflate and press the staple exit region against the interstitial vascular prosthesis. A trigger mechanism can be activated to drive the staples from the staple housing, through the staple exit region, into the interstitial artificial blood vessel and into the blood vessel. The endovascular stapler further includes an output boss penetrating the trigger housing, a guide wire exit port near the distal end of the staple housing, a guide wire channel extending from the guide wire exit port to the output boss, and a guide wire channel And a guide wire extending within. By sliding the staple housing along the guide wire, the staple housing can be guided to a specific location within the blood vessel. The trigger assembly further includes a pusher that operates in engagement with the trigger, which extends from within the trigger housing to the staple exit region, wherein the pusher advances through the staple housing and staples the staples. Configured to extrude from the exit area. The endovascular stapler further includes an actuator having a sloped surface, and the pusher further comprises a sloped surface adjacent to the sloped surface of the actuator, wherein the pusher is advanced by advancing the pusher through the staple housing in a forward direction. The inclined surface of the actuator is brought into contact with the inclined surface of the actuator, and the actuator is moved in a direction substantially perpendicular to the forward movement direction of the pusher. The movement of the actuator can drive the staples through the staple exit area. The stapler further includes a staple stop plate coupled to the staple exit region, the staple stop plate configured to deform the staples before exiting the staple exit region. The pusher further includes a beveled surface on its side that is configured to rotate the staple stop plate away from the staple exit area during advancement of the pusher.

In yet another embodiment, an endovascular stapler for securing an artificial blood vessel to a blood vessel includes a trigger housing including a trigger mechanism; a proximal end on the trigger housing, and a distal end away from the trigger housing A staple housing having a staple channel extending from the proximal end to a staple exit region near the distal end and configured to receive a plurality of staples in tandem; in a trigger housing A pusher extending from the first to the staple channel, wherein when the trigger mechanism is activated, the pusher advances through the staple channel, advances a plurality of staples stored in tandem within the staple channel, and the first staple From the staple exit area. The staple channel includes a bend adjacent to the staple exit area, the bend shaped to shape the staple as the staple is ejected from the staple exit area. The stapler further includes a balloon inflation port extending through the trigger housing, a balloon inflation channel extending within the staple housing and in fluid communication with the balloon inflation port, and a balloon external to the staple housing and in fluid communication with the balloon inflation channel. And the balloon can be selectively inflated and deflated to press the staple exit region against the interstitial vascular prosthesis. The balloon is located on the opposite side of the staple exit area. The stapler further includes an output boss that extends through the trigger housing, a guidewire exit port near the distal end of the staple housing, a guidewire channel that extends within the staple housing from the output boss to the guidewire exit port, and a guidewire The staple housing can be guided to the blood vessel by sliding along the guide wire.

In yet another embodiment, a stapler for stapling a blood vessel is formed from a trigger housing having an internal cavity; a trigger mechanism extending from within the internal cavity of the trigger housing; and from the trigger housing into the elongated staple housing. An elongated staple housing extending to the configured staple exit region and configured to receive at least one staple; a leading portion in the staple housing; and a trailing portion in the internal cavity of the trigger housing A pusher having an inclined surface at its leading end; an actuator having an inclined surface disposed adjacent to the inclined surface of the pusher; and a staple plate mounted in the staple housing between the actuator and the staple exit area; In this case, the leading part of the pusher is moved forward by trigger activation. And the inclined surface of the pusher interacts with the inclined surface of the actuator, forcing the actuator toward the staple exit area, so that engagement with the staple stop plate causes at least one staple to exit the staple exit area. Prior to release, at least one staple is deformed. At least one staple housed within the staple housing may be formed into a W shape that is elongated prior to ejection from the staple exit area.

In yet another embodiment, an endovascular stapler for coupling a stent vascular prosthesis to a blood vessel includes a trigger housing having an elongate staple housing extending therefrom, the elongate staple housing configured to be inserted into a blood vessel. And a staple exit area configured to receive staples. The intravascular stapler further includes a pusher extending from the trigger housing into the staple housing; advancing the pusher within the staple housing to push the staples contained within the elongated staple housing through the staple exit region, A trigger mechanism in the housing configured to couple the blood vessel to the blood vessel; and a balloon adjacent to the staple housing that expands to force the staple exit region toward the stent prosthesis. The stapler further includes a staple stop plate mounted within the staple housing, the staple stop plate configured to form the staples prior to exiting the staple exit area. The staples can be formed in the shape of an elongated W before being released from the staple exit area.

A method for repairing an endovascular prosthesis within a blood vessel using an endovascular stapler having a distal end and a balloon coupled thereto, wherein the method converts the distal end of the endovascular stapler to an interstitial prosthesis. Inserting the balloon; inflating the balloon to press the distal end of the endovascular stapler against the interstitial prosthesis; and releasing the staples from the intravascular stapler into the interstitial prosthesis. .

Another embodiment uses an endovascular stapler having a distal end forming a staple exit region, a trigger for placing staples, and a balloon near the staple exit region to repair an endovascular prosthesis in the blood vessel. In a method, the method includes inserting a distal end of an intravascular stapler into an interstitial prosthesis, inflating a balloon to press the staple exit region against the interstitial prosthesis, and staples into the staple exit region. The insertion type artificial blood vessel and the step of placing in the blood vessel. The method further includes partially deflating the balloon, rotating the endovascular stapler, re-inflating the balloon, and pressing the stapler exit area against the interstitial prosthesis at a location adjacent to the initial staple; Positioning the second staple from the staple exit region into the interstitial artificial blood vessel and the blood vessel.

Another method of performing surgery on a blood vessel having an interstitial artificial blood vessel within the blood vessel includes the steps of providing a plurality of staplers each having a staple housing for storing staples and an inflatable and deflateable balloon; Inserting a staple housing of the first stapler of the stapler into the endovascular prosthesis, inflating a balloon of the first stapler of the plurality of staplers and pressing the staple housing against the endovascular prosthesis; Advance the first staple out of the staple housing;
The initial staple may include an interstitial artificial blood vessel and piercing the vessel wall. The method further includes deflating a balloon, removing a staple housing of a first stapler of the plurality of staplers from the endovascular artificial blood vessel, and interpolating a second staple housing of the plurality of staple housings. Inserting into a vascular prosthesis; inflating a balloon and pressing a second staple housing of the plurality of staple housings against an interstitial vascular region other than the position of the initial staple;
A staple of a second stapler of the plurality of staplers may be advanced from within the staple housing, and the second staple may pierce the interstitial vascular prosthesis in a region other than the position of the initial staple.

According to another aspect of the present invention, an endovascular stapler for securing an interstitial artificial blood vessel to a blood vessel is adapted to receive a plurality of staples therein and release the plurality of staples therethrough. A staple housing having a plurality of exit areas for; a plurality of staple pushers configured to advance the plurality of staples through the plurality of exit areas; and a trigger adapted to advance the plurality of staple pushers; An actuating assembly adapted to release a plurality of staples through a plurality of outlet areas; and when operated in combination with a staple housing near the outlet area to release a plurality of staples, the displacement member causes the outlet area to And a displacement mechanism that is operated to press against the insertion type artificial blood vessel. The plurality of staples may be arranged radially around the longitudinal centerline of the staple housing. Alternatively, a plurality of staples may be arranged linearly within the staple housing.

The subject matter relating to the invention is particularly pointed out and distinctly claimed in the concluding portion of the specification. However, the construction and operation of the present invention, and its features, objects and advantages, will be or will be apparent to those skilled in the art with reference to the following detailed description when read in conjunction with the accompanying drawings. . Any other configurations, methods of operation, features, objects or advantages identified by those skilled in the art are intended to be included herein, within the scope of the present invention, and protected by the accompanying claims. .

2 is a plan view of a handle portion of a stapler according to an embodiment of the present invention. FIG. It is sectional drawing of the stapler of FIG. 1 which shows the internal components. It is a perspective view of the pusher which comprises a part of stapler of FIG. FIG. 2 is a longitudinal cross-sectional view of the distal end of a staple housing that forms part of the stapler of FIG. 1, showing its internal components. FIG. 5 is a cross-sectional view of the distal end of the staple housing shown in FIG. 4 taken along section line AA. FIG. 5 is a cross-sectional view of the distal end of the staple housing shown in FIG. 4 taken along section line BB. FIG. 5 is a cross-sectional view of the distal end of the staple housing shown in FIG. 4 taken along section line CC. FIG. 6 is a longitudinal cross-sectional view of the distal end of the staple housing shown in FIG. 4 taken along section line DD. FIG. 3 is a cut-away cross-sectional view of a patient's abdominal cavity showing a general arrangement of staple housings that form part of a stapler utilized in a method for stopping artificial blood vessel movement according to one embodiment of the present invention. FIG. 6 is a second cut-away cross-sectional view of a patient's abdominal cavity showing a general arrangement of staple housings that form part of a stapler utilized in a method for stopping artificial blood vessel movement according to one embodiment of the present invention. 1 is a cut-away cross-sectional view of a patient's abdominal cavity showing the initial steps of a method for securing an artificial blood vessel into an aortic aneurysm according to an embodiment of the present invention. FIG. 12 is a cut cross-sectional view of the patient's abdominal cavity showing the subsequent steps of the method of securing the artificial blood vessel into the aortic aneurysm of FIG. FIG. 6 is a cross-sectional view of a portion of an intravascular stapler according to a second embodiment of the present invention inserted into the aortic wall. FIG. 6 shows a cross-sectional view of the distal end of a staple housing of a stapler according to a second embodiment of the invention in an initial position. FIG. 15 shows a longitudinal section through the distal end of a staple housing of a stapler according to a second embodiment of the invention in the initial position shown in FIG. 14. FIG. 6 shows a longitudinal section view of the distal end of a staple housing of a stapler according to a second embodiment of the invention in an advanced position. FIG. 17 shows a cross-sectional view of the distal end of the staple housing of the stapler according to the second embodiment of the invention in the advanced position shown in FIG. 16. FIG. 6 shows a longitudinal section view of the distal end of a staple housing of a stapler according to a second embodiment of the invention in a further advanced position. FIG. 19 shows a cross-sectional view of the distal end of the staple housing of the stapler according to the second embodiment of the invention, in the further advanced position of FIG. FIG. 6 shows a perspective view of several internal components that form part of a stapler according to a second embodiment of the present invention. FIG. 6 shows a cross-sectional view of the distal end of the stapler of the present invention according to a third embodiment. FIG. 22b shows a triangular device forming part of a staple housing, FIG. 22b shows a triangular device in a parallel relationship, and FIG. 22a shows a triangular device in an angular relationship, used in accordance with an embodiment of the present invention.

Hereinafter, preferred embodiments of the intravascular stapler of the present invention will be described. In describing the embodiments illustrated in the drawings, specific terminology is used for the sake of clarity. It is understood, however, that the invention is not limited to the specific terms chosen, and that each particular term includes all equivalent techniques that operate in a similar manner to accomplish a similar purpose. There is a need to.

In general, an intravascular stapler includes a staple portion, or staple housing, that is intended to be inserted into a patient's body through the aorta and placed near a vascular wall or artificial blood vessel, such as the aortic wall. To maintain this position, a displacement device such as a balloon can be inflated at the staple portion and the staple portion can be pressed against the aortic wall or artificial blood vessel. Although it is preferred that the displacement device is a non-elastic balloon, an elastic balloon may also be used. Other displacement devices including cobweb elements or multiple rods may also be used. By activating the trigger located on the body of the endovascular stapler that remains outside the patient's body, the staples can be advanced through the aortic wall and the artificial blood vessel. The staple may be pre-formed with some initial curvature or flat. In any case, the staple portion typically includes an compliant element that curves as the staple advances. Next, the staple penetrates the aortic wall and the artificial blood vessel, curves in the planned path so that the leading edge bends back, penetrates the aortic wall and the outside of the artificial blood vessel again, and holds the aortic wall and the artificial blood vessel together To do.

In embodiments where multiple staples can be inserted, the inelastic balloon is deflated, the stapler is rotated to the second position, and the other staples are driven. This process is repeated many times over the entire 360 ° range until a sufficient number of staples are driven and the artificial blood vessel is correctly secured to the aortic wall. This usually requires 8 staples.

In embodiments where the endovascular stapler houses only one staple, the central portion of the stapler is removed, reloaded, and reinserted many times to drive the plurality of staples. Alternatively, several preloaded staplers can be prepared. After releasing the staples from the first stapler, the stapler is removed and discarded, and the second stapler is inserted. This process can be repeated until a sufficient number of staples are driven. Thus, surgical staff typically prepare up to eight preloaded staplers for each procedure and use each stapler in turn.

The intravascular stapler of the present invention may be an “on wire” instrument such as a 10 French sheath designed to fit through the typical sheath of aortic and iliac artery use. It is also possible to downsize the stapler to fit through a small sheath for securing the artificial blood vessel in a smaller diameter blood vessel.

In some embodiments, the stapler fires a plurality of staples in sequence. In such a case, the staples can be constructed in a special precut of an alloy such as Phynox, which is stacked in tandem within the staple channel and has sufficient column strength to be sequentially pushed through the channel. In certain embodiments of the invention, the staples must be sufficiently flexible so that they can easily follow a curved internal staple guide.
In other embodiments, the staples must be loaded individually. In yet another embodiment, staples are automatically loaded from the cartridge, but are not stacked in tandem and reside side by side in the cartridge.

Generally, the stapler is introduced through the inguinal sheath or other suitable access into the lumen of the interstitial artificial blood vessel. Its leading element goes to the proximal end of the interstitial prosthesis, but the prosthesis must be accurately identified. An ultrasonic probe can be used for such identification. For future interstitial vascular prostheses, clearly mark the end of the vascular fabric with a thread that does not pass radiation. For older artificial blood vessels, radiation techniques such as roadmaps can be used to locate the end of the artificial blood vessel. As is known in the art, multiple guide wires may be used during surgery.

When the staple portion of the stapler is aligned with the proximal end of the interstitial prosthesis, the stapler head may be forced against the interstitial prosthesis and the vessel wall, preferably by inflation of an inelastic balloon. In this position, a single stroke of the stapler trigger preferably produces a forward displacement of the staple pusher sufficient to advance a staple through the vascular prosthesis and the vessel wall.

In one embodiment, the curvature of the staple guide forms an arc or spiral in the staple having a single piercing point at the beginning of the staple. In other embodiments, the staple can form an exaggerated W. In this case, when the staple is deformed by the staple stop plate, each end of the staple pierces the insertion type artificial blood vessel and the blood vessel wall.

In the case of a stapler where the staples are automatically loaded in tandem, the stapler handle trigger is ratcheted and pulls the hammer for the next firing. The specific ratcheted design of pushers and triggers means that when the hammer is fully raised, pulling the trigger once will completely position the leading staple and place the subsequent staple segment at the tip of the curved staple guide. The pusher accurately performs the reciprocating motion necessary to place and fire the next staple. In a single staple design, the stapler can be retracted and loaded with staples prior to firing the second staple. Alternatively, additional staplers can be used during a single procedure, each firing only one staple. When firing multiple staples from a cartridge that holds the staples side-by-side, the trigger ratchet mechanism includes a configuration that allows the pusher to be pulled into the stapler body, and after the previous staple firing, the stapler In position for firing staples.

Preferably, the inelastic balloon is inflated and deflated manually or using any of a number of instruments used to inflate and deflate the angioplasty balloon. Liquids such as diluted contrast media or physiological saline can also be used to expand the balloon.

After each staple is deployed, the balloon is partially deflated, the stapler is rotated, and this step is repeated to deploy the next staple. In an embodiment where the staples are vertically aligned, the only limiting factor in the number of staples per instrument, and hence the length of the instrument, is that the staples in the row are individually driven by subsequent staples and finally the reciprocation of the staple pusher It is driven by the column strength of the staple alloy. It will be apparent that the staples must have sufficient column strength so that they do not deform in the stapler prior to use. It is also clear that a single staple must push several preceding staples.

In embodiments in which the staples are stored in tandem, the staples can be scored such that the diamond tip of each subsequent staple fits into a diamond shaped cavity formed at the end of each preceding staple. In instruments that use a single staple, or instruments that use side-by-side staple cartridges, the column strength of the individual staples is less of an issue. Of course, however, the strength needs to be sufficient to adequately secure the stent vascular prosthesis.

Referring to the drawings, FIG. 1 illustrates an intravascular stapler 100 according to one embodiment of the present invention. As shown, the stapler 100 is generally shaped like a gun. The stapler 100 includes a housing 102 having a handle 104 and a trigger 1 extending from the housing.
06 may be included. The housing also includes a barrel 101 having an output opening 110.
The input boss 108 can be located at the rear 103 of the housing 102. A guide wire 112 may extend into the input boss. Extending from the output opening 110 may be a staple housing 114. Stapler 100 also includes a balloon inflation port 116.

FIG. 2 shows a cross-sectional view of the stapler 100 of FIG. As shown, the trigger 106 can include an inner portion 105 and an outer portion 107. The inner part 105 has a housing 1
A 02 outer grip 109 is also included. The inner part 105 is provided with a trigger 106 in the housing 1.
Also included is a pin 128 that attaches to 02, around which the trigger can rotate. The trigger 106 also includes a spring mechanism (not shown) for biasing the trigger 106 away from the handle 104. The outer portion 107 of the trigger 106 is attached to the inner portion with a spring 132. Advantageously, the outer part 107 is displaceable relative to the inner part 105 and compresses the spring 132. The toothed element 126 of the outer part 107 has an inclined part 138 and an edge or lip 1
40 are included. As discussed below, the inclined portion 138 of the tooth 109.
Each assists the ratchet operation of the trigger 106.

The ratcheted stapler pusher 120 can bend between the trigger 106 and the path created by the internal cavity 118 formed from the housing 102. Pusher 120
Includes a ratcheted portion 122 as a subsequent portion and a cylindrical portion 1 as a leading portion.
24 is included. The ratcheted portion 122 includes a toothed element 1 of the stapler trigger 106.
An inclined portion 138 that can be engaged with 26 is included. Activation of the stapler trigger 106 that initiates rotation of the toothed element 126 about the pin 128 causes the pusher 120 to move through the barrel 101 toward the distal end 130 of the stapler 100 (FIG. 4). When trigger 106 returns to its initial position, spring 132 pawls toothed element 126 and pusher 120 remains in its advanced position. The ratcheted portion 122 of the pusher 120 may be stored in a spiral shape within a staging area 134 located within the handle 104 of the stapler 100.

FIG. 2 shows the internal components of the input boss 108. Input boss 108 is housing 102
Including a flange 111 formed from The flange includes an internal cavity 118 of the housing 102.
A cavity 113 extending therein is included. Within the cavity 113 near the flange 111, there may be a pair of rubberized elements 115 having a boundary 117 therebetween. Guide wire 112
(FIG. 1) can be passed along the boundary from the exterior of the housing 102 into the internal cavity 118. Once inside the interior cavity 118, the guide wire passes through the barrel 101 and guide wire channel 144 (FIG. 4) of the staple housing 114 as discussed below.
Can be stretched.

FIG. 3 shows a perspective view of the pusher 120. This figure clearly shows the cylindrical portion 124 in front of the pusher 120 and the ratcheted portion 122 at the rear of the pusher. Ratcheted portion 122 is a series of ramps 136 having ramped portions 138 that terminate in lip 140.
May be included. As will be discussed, the toothed element 126 of the stapler trigger 106 incorporates teeth 109 having a similar size and shape as the angled portion 138. These elements mesh with each other to facilitate the displacement of the pusher 120 when the trigger 106 is started, but the trigger can be ratcheted on the return stroke.

FIG. 3 also shows the front surface 119 of the pusher 120. As discussed below, pusher front surface 119 can be configured to contact and advance a series of staples 148 (FIG. 4).

FIG. 4 shows a longitudinal cross-sectional view of the distal end 130 of the staple housing 114. As shown, the staple housing 114 may contain a staple channel 142, a guidewire channel 144, and a balloon inflation channel 146. Each channel is generally cylindrical and typically runs the entire length of the staple housing 114 from the outlet opening 110 of the housing 102 to the distal end 130 of the staple channel 146.

Typically, the staple channel 142 houses a series of staples 148 placed in tandem, including first staples 148a and second staples 148b. Each staple preferably has a pointed proximal end 150 and a distal end 152 having a cavity or indentation 154 that conforms to the pointed proximal end. Thus, the leading staple cavity, such as the first staple 148a, can be filled with the pointed proximal end 150 of the next staple, such as the second staple 148b.

As discussed, stapler 100 is generally used to fire a plurality of staples 148 in sequence to secure an artificial blood vessel to a blood vessel. Staples 148 are formed of a special alloy precut such as Finox with sufficient column strength, and staple channels 14
Preferably, they are placed in tandem within 2 and extruded by subsequent staples. It is also preferred that each of the staples 148 is sufficiently flexible to easily follow the curved inner staple guide 151.

For example, when the trigger 106 is activated, the pusher 120 causes the first staple 148a to be activated.
Is extruded by the second staple 148b and the subsequent staples. As the first staple moves along the staple channel 142, the staple begins to bend in the direction of the distal end 130 of the staple housing 114 due to the bent portion 153 of the staple channel 142. The staple 148 present in the bent portion is the inner staple guide 151.
It will be appreciated that the bent portion 153 of the staple housing is bent so as to pre-curve upon entering. As discussed below, as the staple 148 passes through the staple guide 151, the staple continues to be shaped to form a loop that can penetrate each of the artificial blood vessel and the blood vessel in at least two locations.

Guidewire channel 144 extends parallel to and adjacent to staple channel 142 along the entire length of staple housing 114. The guide wire channel becomes the housing of the guide wire 112, and the guide wire is the distal end 1 of the stapler 100.
Used to advance 30 to a position where stapling is performed.

In general, the intravascular stapler 100 is believed to advance via an “on wire” type system. As an “on wire” instrument, the staple housing 114 portion of the stapler 100 is designed to be guided in a blood vessel following the path of a pre-installed guide wire 112. For example, the guide wire 112 may be placed in the artery by surgery. The distal end 130 of the staple housing 114 is then guided through the guidewire 1
12, the guide wire travels from the guide wire exit point 155 at the distal end 130 through the guide wire channel 144 and out of the input boss 108 of the housing 102. As soon as the distal end 130 reaches its end, advancement of the staple housing stops and the stapler 100 is ready to deploy the staple 148. To be able to bend along the path, if necessary, toward the area where the staple 148 is deployed,
It is understood that the staple housing 114 can be constructed of a flexible material.

The endovascular stapler of the present invention is designed to fit through a 10 French sheath for use in the aorta and iliac arteries. However, it can also be foreseen that the stapler can be miniaturized to fit a smaller sheath in order to fix the interstitial artificial blood vessel in a smaller diameter blood vessel.

Also shown in FIG. 4 is the balloon inflation channel 146 of the staple housing 114. Extending from the balloon inflation channel 146 is an inelastic balloon 156. In the view of FIG. 4, an inflatable inelastic balloon 156 is shown. In the deflated state, inelastic balloons are generally very thin and typically fit nicely into the balloon inflation channel 146.

Inelastic balloon 156 can be inflated prior to firing of staple 148. One purpose of inflating the inelastic balloon 156 is to move the staple exit area 158 of the staple housing 114 toward the area where the staples 148 are fired. This does not place the staple 148 immediately adjacent to the receiving area, but rather the staple 148.
This is to help prevent the staple housing 114 from moving linearly or rotating during the firing.

Selective inflation and deflation of the inelastic balloon 156 is achieved through the balloon inflation port 116 of the housing 102. It will be appreciated that the balloon inflation port 116 includes a valve (not shown) on which a liquid source (not shown) is mounted. A liquid source flows into the balloon inflation port 116 and inflates the inelastic balloon 156. The liquid is discharged from the inelastic balloon 156 by using a liquid source that has the function of opening the valve or reversing the direction of flow to create a vacuum, thereby releasing the liquid from the inelastic balloon. 156 deflation occurs at the balloon inflation port 116. It will be appreciated that the balloon inflation port 116 is in fluid communication with the inelastic balloon 156 via the balloon inflation channel 146. Inflation and deflation can be performed with any effective device used in the inflation and deflation of angioplasty balloons. Typically, the liquid used to inflate and deflate the balloon is a diluted contrast agent or saline.

When the staple 148 is fired, the inelastic balloon 156 is deflated and the staple housing 114 is rotated to a second position in preparation for firing the second staple 148. Second staple 1
Prior to firing 48, the inelastic balloon 156 is reinflated and the staple exit region 158 of the stapler 100 is in place for firing.

FIG. 5 shows a cross-sectional view of staple housing 114 made along section line AA of FIG. In FIG. 4, the inelastic balloon 156 is shown inflated. As shown in FIG. 5, the guidewire channel 144 is connected to the staple housing 11 around the staple exit area 158.
4 is stepped (also shown in FIG. 4). This step forms a staple guide 151 along the curved region 153 of the staple channel 142 and the longitudinal center line of the staple housing 114.

6 shows a cross-sectional view of the staple housing 114 taken along section line BB of FIG. FIG.
As shown, the cutting line BB is taken closer to the housing 102 than the cutting line AA. In this cross-sectional view, the staple exit area 158 is not yet visible. However, the staple 148 in the staple channel 142 and the guide wire 1 in the guide wire channel 144
12 is clearly visible. Further, the inelastic balloon 156 is shown in an inflated state.

FIG. 7 shows a cross-sectional view of staple housing 114 along section line CC in FIG. In this upstream portion, it is clearly shown that the staple channel 142, guidewire channel 144 and balloon inflation channel 146 are all stacked on a single vertical axis within the staple housing 114. This arrangement constitutes the arrangement of the various channels 142, 144, 146 for most lengths of the staple housing 114.

FIG. 8 shows a longitudinal cross-sectional view along section line DD of the distal end 130 of the staple housing 114 shown in FIG. In this view, the staple exit area 158 is the staple housing 11.
It is clearly shown with the proximal end 150 of the staple 148 closest to the distal end 130 of the four. The guide wire channel 144 is stepped with the guide wire 112 to form a staple exit region 158.

FIG. 9 shows the staple housing 114 inserted into a sheath within the human body. Staple housing 114 is typically introduced into the buttocks or other suitable access area, where the staple housing follows the previously inserted guidewire 112 and into the lumen within the interstitial prosthesis to be sutured. Is inserted. FIG. 9 also shows the inelastic balloon in a fully inflated state. As discussed above, the distal end 130 of the staple housing 114 is pushed toward the aortic sidewall by the inelastic balloon 156. When so extruded, the first staple 148a is fired. Subsequent staples 148 are fired after the inelastic balloon 156 is deflated, the staple housing 114 is rotated, the inelastic balloon is inflated, and the staple exit region 158 is aligned with the intended deployment position.

FIG. 10 is an enlarged cross-sectional view of the distal end 130 of the endovascular stapler 100 in use. As previously discussed, the distal end 130 of the stapler 100 can be inserted through the sheath (not shown) along the guide wire 112 into the aorta 160. The distal end 130 is then placed over the aortic aneurysm 162 to be treated. As previously discussed, the inelastic balloon 156 is then inflated to press the staple exit region 158 of the stapler 100 against the interstitial vascular prosthesis 164 and the aortic sidewall 160 as shown in FIG.

FIG. 11 shows a longitudinal section of this arrangement showing the internal components of the staple housing 114. In this figure, the first staple 148a is moved to the staple channel 1 by the second staple 148b.
It is clearly shown being pushed through 42 curved regions 153. Such curvature of the staple channel deforms the first staple 148a and allows the staple to bend around the curved inner staple guide 151 toward the staple exit region 158. Adjacent to the area where staples 148 are deployed, staple exit area 15
8 is shown again. Inflating the inelastic balloon 156 ensures that the staple exit area 158 is installed.

FIG. 12 shows a longitudinal cross-sectional view of FIG. 11 after firing the staple 148. As shown in the figure,
The internal staple guide 151 forms the staple 148 into a ring or loop shape, engages the insertion type artificial blood vessel 164 and the aortic side wall 160 from the inside of the aorta 160, and then reverses the aortic side wall 160 and the insertion type artificial blood vessel. Re-engage 164 from outside the aorta. As discussed above, the inelastic balloon 156 is temporarily deflated and the staple housing 114 is rotated into a position to fire the second staple 148b.

The stapler is introduced into the patient, typically through an inguinal sheath or other suitable access within the lumen of the interstitial vascular prosthesis. The stapler is advanced to the proximal end of the endovascular prosthesis that needs to be accurately identified. For future interstitial vascular prostheses, the end of the vascular fabric is clearly marked with a radiopaque thread. For older instruments, radiation techniques such as road mapping can be used to position the end of the artificial blood vessel. As is known in the art, multiple guide wires may be used during surgery.

When the stapled end of the stapler is aligned with the end of the insertion type artificial blood vessel, the stapler head is forced to abut against the insertion type artificial blood vessel and the blood vessel wall by inflation of the balloon. Pulling the stapler trigger in this position causes a forward displacement of the staple pusher sufficient to advance one staple through the vascular prosthesis and the vessel wall. Due to the curvature of the staple guide, the staple forms an arc. The stapler handle is then triggered for the next firing. Due to the special ratcheted design of this pusher and trigger, when the hammer strikes sufficiently, pulling the trigger fully deploys the leading staple, and the trailing staple portion is curved at the predetermined end of the curved staple guide. The exact pusher movement required to place it is performed.

The preferred inelastic balloon inflation can be performed manually or with any of a number of available instruments used for inflation of angioplasty balloons. Liquids such as diluted contrast media or saline can be used to inflate the balloon.

After each staple is deployed, the balloon is deflated, the stapler is rotated and the above steps are repeated to deploy the next staple. The only limiting factor in the number of staples per appliance, and hence the length of the appliance, is that the staple columns are aligned because the staples in the row are each driven by subsequent staples, and ultimately the movement of the staple pusher. It is strength.

The staple is cut so that the diamond-shaped tip of the subsequent staple fits into a diamond-shaped cavity formed at the end of the leading staple.

FIG. 14 is a partial cross-sectional view of a staple housing 214 of an intravascular stapler (not shown) according to a second embodiment of the present invention. In this embodiment, a single staple 248 formed in the shape of an elongated W is applied to secure the artificial blood vessel 264 to the blood vessel shown in FIG. Typically, the main function of the stapler according to the present embodiment is to stop the movement of the previously inserted endovascular artificial blood vessel. Other embodiments that use multiple elongated W-shaped staples can also be used to stop the migration of previously implanted endovascular prosthesis or to fix a new interstitial prosthesis. In yet another embodiment,
The portion of the stapler that can replace the pre-loaded staple for subsequent firing can be retrieved.

FIG. 13 shows a partially cut-away cross-sectional view of the stapler housing 214 and inelastic balloon 256 inserted into the aortic wall 260 when preparing to attach the stent vascular prosthesis 264.
As shown in FIG. 13, in the “on wire” type system discussed above, the staple housing 214 can be translated along the guide wire 212 and placed in place. When the staple exit area 258 is correctly positioned so that it is adjacent to the intended deployment area, the inelastic balloon 256 is inflated as shown in FIG. 13 and urges the staple exit area toward the stent vascular prosthesis 264, sequentially. Press against wall 260. Staple 248 is then fired and staple housing 214 is removed. As with other embodiments of the present invention, firing of staples 248 can be performed utilizing a housing having a ratcheted trigger.

As shown in FIG. 14, the staple housing 214 includes an outer casing 300 having a staple exit region 258 at its distal end 230 (FIG. 15). Pusher 220
Can extend the entire length of the outer casing 300 from the stapler to the staple exit area 258. As shown in FIG. 15, the pusher 220 has a staple exit area 25.
8 includes a narrowed portion 302 adjacent to 8. The tapered portion 302 includes an inclined surface 304. Adjacent to the inclined surface 304 is an actuator 306.
It is. The actuator 306 includes an inclined surface 308 adjacent to the inclined surface 304 of the tapered portion 302.

Returning to FIG. 14, the staple plate 310 is shown in the outer casing 300. Although not shown in the figure, the staple stop plate 310 is connected at one end to the outer housing 300 by a rotatable connection, such as a hinge 312 placed on the housing or a protruding portion of the housing. Two such protrusions may also support a rod around which the stop plate 310 is rotatable and to which the stop plate 310 is coupled. The rod may spin the protruding portion or may be coupled to the protruding portion with an internal spacing of the rod.

The second end 314 of the staple stop plate 310 extends toward the staple exit area 258 and can divide the staple exit area into a first staple exit area 258A and a second staple exit area 258B as shown in FIG. A spring 313 is attached between the outer casing 300 and the staple stop plate 310, and the stop plate is biased to the position shown in FIG. 14 where the spring is fully extended. As discussed below, when compressive force is applied to the spring 313,
The stop plate 310 can rotate from that position.

Similar to the first embodiment, the guide wire channel 244 is also a staple housing 214.
Located in. Guidewire channel 244 allows guidewire 212 to be used in an “on wire” system, and staple exit area 258 can be in place.

FIG. 14 also shows the inelastic balloon 256 portion. The inelastic balloon 256 of the second embodiment may be completely outside the staple housing 214. The non-elastic balloon 256 is intended to be inflated so that the staple housing 214 is pushed toward the stent vascular prosthesis 264 and the stent vascular prosthesis is tightly accessible to the aortic wall 260.

The staple housing 214 also includes an elongated W-shaped staple 248. As shown in FIG. 15, the staple 248 has two U-shaped portions 316 connected by a bridge 318.
Is included. Each U-shaped portion 316 of the staple 248 is an actuator 306.
Sitting on the front surface 320 of the At the forefront of staple 248, front surface 320 protrudes to form flange 324, which serves to capture and secure the staple in place. Further, as shown in FIG. 14, the actuator front surface 320 is curved to assist in securing the staples 248 in place.

Activation of the stapler trigger advances the ratcheted stapler pusher 220 toward the distal end 230 of the staple housing 214. As shown in FIG. 16, advancement of the pusher 220 toward the distal end 230 of the staple housing 214 causes the inclined surface 304 of the pusher to contact the inclined surface 308 of the actuator 306. As pusher 220 is advanced, the interaction between inclined surfaces 304, 308 pushes front surface 320 of actuator 306 vertically toward staple exit region 258. As shown in FIGS. 16 and 17, as the actuator 306 advances, the bridge 318 of the staple 248 is pushed toward the second end 314 of the staple stop plate 310. This advancement moves the U-shaped portion 316 of the staple 248 into the axis of the bridge 318 and the actuator 306.
Flattened along the front surface 320 of the substrate. The other portion of the U-shaped portion 316 extends from within the staple housing 214 so that the sharpened distal end 252 of the staple can penetrate the insertable prosthesis 264 and the aortic wall 260.

Referring briefly to FIG. 20, a pusher 220 according to a second embodiment of the present invention is shown with a raised portion 324 on its side 326. The raised portion 324 includes a transition region 328 that descends obliquely toward the flat surface of the side 326 of the pusher 220. When the pusher 220 is displaced, the raised portion 324 moves toward the central portion 313 of the staple plate 310.
As soon as the transition region 328 contacts the central portion 313 of the staple plate 310, the staple plate rotates about its first end 311 at the hinge 312 and compresses the spring 313 to compress the second plate of the stop plate.
The end 314 is no longer in contact with the staple 248.

FIG. 19 shows a partial cross-sectional view of the staple housing 214 of the endovascular stapler, with the pusher 220 advanced and lifted 324 in contact with the staple stop plate 310. It will be understood that the advancement of the pusher 220 and the displacement of the staple stop plate 310 are performed against the biasing force of the spring 313.

18 shows that pusher 220 is in a fully advanced position, but staple stop plate 310 is no longer in contact with staple 248. FIG. As shown in FIG. 18, before the staple stop plate 310 is rotated away from the staple 248, the U-shaped portion 3 of the staple 248 is removed.
It can be seen that 16 is curved, the sharpened tip 251 of the staple extends into the aortic wall 260 and the bridge 318 extends to include the U-shaped portion to form a closed staple.

The endovascular stapler disclosed with respect to the second embodiment of the invention is a single staple 2
48 is fired. As disclosed, when subsequent staples 248 are required, the entire staple housing 214, possibly including the inelastic balloon 256, is removed from the body and loaded with a second staple. Once loaded, the staple housing 214 and, if necessary, the inelastic balloon 256 are reinserted into the body and the second staple 248 is fired. This procedure can be repeated as often as necessary to stop the movement of the endovascular prosthesis or to completely fix the new prosthesis. Instead of reloading the endovascular stapler, the surgeon may choose to prepare multiple endovascular staplers and use each in turn without re-loading. It will be appreciated that providing multiple intravascular staplers saves time at the surgical site where it is desirable to minimize the duration of the surgery.

In another embodiment shown in FIG. 21, a housing 330 may be disposed between the staple housing 214 and the inelastic balloon 256. Such a housing 330 allows the staple housing 214 to be pulled out leaving a cavity in the housing 330 and the staple housing to be returned after the next staple is loaded (or second).
Or a subsequent staple housing can be inserted). The inelastic balloon 256 can then be partially deflated and the staple exit area 258 can be rotated to the next position for firing subsequent staples 248. In this way, additional staples 248 after the first staple can be inserted in a relatively fast manner compared to other embodiments in which the inelastic balloon 258 is removed and reinserted.

In yet another embodiment, additional staples can be mounted on a cartridge in the staple housing 214 and the instrument with the additional staples can be automatically reloaded. In that case, a mechanism for disabling the ratchet function of the stapler trigger is included in the stapler housing, and the pusher is pulled from the position shown in FIG. 18 to the position shown in FIG. Once in Figure 1
When retracted to the position shown in FIG. 5, it is expected that the spring loaded stapler feed mechanism will automatically reload the actuator with additional staples. Preferably, the autoloader can supply up to 7 staples so that a total of 8 staples can be fired without removing the staple housing. It will be appreciated that eight staples are generally sufficient to connect an artificial blood vessel to a blood vessel. Of course, a loading device capable of supplying a larger number of staples may also be provided.

In yet another embodiment, multiple staples can be fired simultaneously from a single staple housing 214. In such an embodiment, the staple housing 214 may include a plurality of staples 316 arranged radially around the centerline of the staple housing. The staples 316 may be arranged side by side in a linear relationship. Each of the staples 316 can be placed simultaneously by the interaction of the pusher 220 and the actuator 306. In such an embodiment, the staple housing 214 preferably includes a staple stop plate 310 for each staple to be deployed. For example, in an embodiment using two staples 316, the staple stop plate 310 may be mounted on each side of the pusher 220 with a separate hinge 312. Each stop plate 310 is on the opposite side of the pusher 220 and can rotate freely without interfering with each other.

In addition to using a balloon, such as an inelastic balloon, to abut the staple exit region of the staple housing against the vessel wall or artificial blood vessel, other means may be employed. For example, a simple triangle device 400 may be used as shown in FIGS. 22a and 22b. Device 400 may include two elongate rods 402, 404. The first end 406 of the first rod 402 can be pivotally attached to the distal end 130 of the staple housing 114 with a pin 408. The second end 410 of the first rod 402 can be pivotally attached to the first end 412 of the second rod 404 with a pin 414. Finally, the second end 4 of the second rod 404
16 can slide in engagement with the staple housing 114. This sliding engagement can be performed using a pin 420 slidable in a groove 422 created in the staple housing. The handle 418 can extend the length of the staple housing 114 to the housing 102 of the stapler 100.

Typically, when the rods 402, 404 are parallel to the longitudinal axis of the staple housing, as shown in FIG. 22b, they are in close contact with the outer wall of the staple housing 114 and adjacent to the staple housing 114. When the handle 418 is pushed forward toward the distal end 130 of the stapler 100, the pivot point between the first rod 402 and the second rod 404 located on the pin 414 as shown in FIG. It is understood that it is forcibly extended from the outer wall. If the pivot point 414 contacts the inner wall of the blood vessel, the opposite side of the staple housing is forced away from the inner wall portion contacting the pivot portion. Thus, the device can be mounted on the opposite side of the staple exit area 158 to bring the staple exit area closer to the vessel wall at a predetermined area. Of course, a plurality of such triangular devices or parallelograms with more than three sides including additional parts may be used. This type of displacement device may be preferred for certain applications because it does not completely occlude or close the blood vessel so that blood flow continues.

Further, although not shown, it will be appreciated that, similar to the balloon inflation channel discussed above, in other embodiments, the handle 418 can be placed in a channel that extends through the interior of the staple housing.

Although the present invention has been described with reference to particular embodiments, it is to be understood that these embodiments are merely illustrative of the principles and applications of the present invention. Accordingly, it is to be understood that numerous modifications can be made to the described embodiments, and that other configurations can be devised without departing from the spirit and scope of the invention as defined by the appended claims. .

In this regard, elements such as triggers have been described in a specific manner. It should be understood that the trigger mechanism and others similar thereto may be manufactured differently. For example, a simple dial advance mechanism can be used instead of a trigger to displace the pusher within the stapler cavity. In such a case, the dial gear ratio can be designed to advance the staple pusher by a fixed distance adjusted by the length of one staple after a predetermined number of turns of the dial.

  The present invention has application in the field of intravascular staplers.

Claims (5)

An endovascular stapler for stapling an interstitial artificial blood vessel or blood vessel,
A trigger housing having an internal cavity;
A trigger mechanism extending from within the internal cavity of the trigger housing;
An elongated staple housing extending from the trigger housing to a staple exit area and adapted to receive at least one staple;
A pusher having a leading portion located in the staple housing and a trailing portion located in the internal cavity of the trigger housing and having an inclined surface in the leading portion;
An actuator having an inclined surface disposed adjacent to the inclined surface of the pusher;
A staple stop plate provided in the staple housing so as to be detachably attached to the at least one staple between the actuator and the staple exit region;
By the operation of advancing the preceding portion of the pusher by the trigger mechanism, the inclined surface of the pusher interacts with the inclined surface of the actuator, and the actuator is forcibly moved toward the staple exit region. Whereby the at least one staple locked by the staple stop plate is configured to be deformed before being released from the staple exit area.   The staple exit region has a long hole shape extending in a longitudinal direction of the staple housing, and the at least one staple is formed in a pre-extended W shape and stored in the staple housing. The intravascular stapler described in 1.   The intravascular stapler according to claim 1, further comprising a balloon configured to inflate adjacent the staple housing to press a staple exit region of the staple housing against a vessel to be stapled.   The intravascular stapler according to claim 3, wherein the balloon is an inelastic balloon.   The pusher includes a side inclined surface on a side surface of the preceding portion, and the side inclined surface abuts against the staple fixing plate during advancement of the pusher to separate the staple fixing plate from the staple exit region. The endovascular stapler according to any one of claims 1 to 4, configured to be detached from the at least one staple.

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