The present invention relates to an apparatus for delivering an implantable prosthesis and, in particular, to an apparatus for simultaneously introducing multiple self-expanding stents to desired locations within a duct.
Self-expanding stents are used for a variety of applications. For example, self-expanding stents are used within the biliary tree to open strictures and maintain the patency of the duct. Current biliary and pancreatic self-expanding stent delivery systems generally include an introducer catheter with a single self-expanding stent loaded at the distal end thereof. A pusher catheter is used to deploy the stent from the distal end of the introducer catheter. In particular, the introducer catheter is retracted in a proximal direction relative to the pusher catheter to expose the stent from the end of the introducer catheter. As the stent is exposed from the end of the introducer catheter, it expands to engage the interior of the duct. The introducer and pusher catheters are then retracted and removed from the patient.
While current stent delivery systems are effective, they are limited to delivering a single self-expanding stent at one time. Thus, if a second stent is required to be deployed at or near the target site within the patient, the original stent delivery system must be retracted and removed from the patient before a second stent delivery system can be introduced and directed back to the target site within the patient. This can be a time consuming task because of the time required to first remove the original stent delivery system and then deliver the second stent delivery system to the target site. In addition, removal and replacement of the original stent delivery system may result in the loss of access to the target site. For example, the wire guide over which the stent delivery system is typically advanced and retracted may be inadvertently pulled from the target site during the exchange of stent delivery systems. If this occurs, then access to the target site will need to be re-established, thereby further increasing the duration and complexity of the medical procedure.
One example of a procedure requiring the deployment of two or more self-expanding stents is the treatment of a stricture in each leg of a bifurcated duct. As explained above, current self-expanding stent delivery systems can only deploy a single self-expanding stent. Thus, it is necessary to introduce a first stent delivery system into the first leg of the bifurcated duct and deploy the first stent therein. The first stent delivery system is then retracted and removed from the patient before a second stent delivery system can be introduced into the second leg of the bifurcated duct to deploy the second stent therein.
What is needed is a stent delivery system that can simultaneously deliver multiple self-expanding stents to a target site within a patient. What is also needed is a stent delivery system that can simultaneously deliver a self-expanding stent into each leg of a bifurcated duct. The present invention meets this need by providing an apparatus and method for deploying multiple self-expanding stents to one or more target sites within a patient, including each leg of a bifurcated duct.
Accordingly, the stent introducer apparatus of the present invention comprises a primary stent introducer device movably disposed within a secondary stent introducer device. The primary stent introducer device includes a first self-expanding stent mounted on an elongate pusher member. The primary stent introducer device further includes an inner introducer catheter slidably disposed about the pusher member and the first stent. The inner introducer catheter, when disposed about the first stent, maintains the first stent in a compressed pre-deployment state. The pusher member is configured to hold the first stent stationary during movement of the inner introducer catheter relative to the pusher member and the first stent. The first stent is deployed by retracting the inner introducer catheter proximally relative to the pusher member to thereby expose the first stent from the distal end of the inner introducer catheter. Once exposed, the first stent self-expands to its deployed state.
The secondary stent introducer device includes a second self-expanding stent mounted within an outer introducer catheter. The outer introducer catheter, when disposed about the second stent, maintains the second stent in a compressed pre-deployment state. The outer introducer catheter is slidably disposed about the inner introducer catheter of the primary stent introducer device. The primary stent introducer device is configured to engage and hold the second stent stationary during movement of the outer introducer catheter relative to the primary stent introducer device and the second stent. The second stent is deployed by retracting the outer introducer catheter proximally relative to the primary stent introducer device to thereby expose the second stent from the distal end of the outer introducer catheter. Once exposed, the second stent self-expands to its deployed state.
In a first embodiment of the invention, the pusher member comprises a distal end cap configured to engage the proximal end of the second stent. In particular, the distal end cap comprises an outer flange that closely but slidably engages with the interior surface of the outer introducer catheter. A support element projects distally from the distal face of the flange and is spaced inwardly from the interior surface of the outer introducer catheter a distance sufficient to accommodate the second stent therebetween. The support element helps to align and maintain the proximal end of the second stent against the flange during deployment of the second stent. In an alternative embodiment of the invention, the outer periphery of distal end cap is disposed within the distal end of the inner introducer catheter. In this alternative embodiment, the proximal end of the second stent is engaged by the distal end of the inner introducer catheter during deployment of the second stent.
In the first embodiment of the invention, the outer introducer catheter comprises a side port through the side wall thereof. The side port is located proximal to and near the proximal end of the second stent, and is sized to allow passage of the primary stent introducer device therethrough. In one aspect of the invention, the secondary stent introducer device is positioned within one leg of a bifurcated duct, while the primary stent introducer device is extended out through the side port and positioned within a second leg of the bifurcated duct.
In the first embodiment of the invention, the pusher member of the primary stent introducer device includes a lumen extending therethrough. The lumen is sized to accommodate a wire guide that may be used to introduce and position the stent introducer apparatus. For example, the wire guide may be used to position the secondary introducer device within one leg of a bifurcated duct. The wire guide may then be used to position the primary introducer device within another leg of the bifurcated duct. The lumen may also be used to introduce fluids to or remove fluids from the target site. For example, the lumen may be used to inject contrast media into the target site to facilitate fluoroscopic viewing of the area.
According to one aspect of the invention, the stent introducer apparatus is used to deploy a self-expanding stent into each of two legs of a bifurcated duct. The stent introducer apparatus is first introduced into the patient by passing it over a previously placed wire guide. This is accomplished by inserting the proximal end of the wire guide into the distal end of the stent introducer apparatus and through the lumen of the pusher member. The distal portion of the stent introducer apparatus, and more particularly the distal portion of the secondary stent introducer device, is advanced along the wire guide until it is positioned in one leg of a bifurcated duct. The distal end of the wire guide is then withdrawn into the distal end of the secondary stent introducer device to a location proximal of the side port in the outer introducer catheter. The wire guide is then advanced out through the side port and into the other leg of the bifurcated duct. Once the distal end of the wire guide has been positioned within the target site in the second duct, e.g., adjacent a stricture, the primary stent introducer device is extended along the wire guide and into the second duct. The first stent is then positioned and deployed at the target site by retracting the inner introducer catheter proximally relative to the pusher member to expose the stent from the distal end thereof.
Once the first stent has been deployed, the primary stent introducer device is retracted back through the side port and into the outer introducer catheter. The wire guide is likewise retracted back through the side port and into the outer introducer catheter. The primary stent introducer device is then advanced distally through the outer introducer catheter, past the side port, and into engagement with the second stent. If desired, the wire guide may then be re-advanced through and beyond the distal end of the outer introducer catheter to allow for re-positioning of the secondary stent introducer device within the first duct. The second stent is then positioned and deployed at the target site of the first duct by retracting the outer introducer catheter proximally relative to the primary stent introducer device, which acts as a pusher for the second stent, to expose the second stent from the distal end thereof. The entire stent introducer apparatus may then be retracted and removed from the patient.
According to another aspect of the invention, the stent introducer apparatus is used to deploy two self-expanding stents into a single duct. The stent introducer apparatus is introduced into the patient by passing it over a previously placed wire guide. This is accomplished by inserting the proximal end of the wire guide into the distal end of the stent introducer apparatus and through the lumen of the pusher member. The distal portion of the stent introducer apparatus, and more particularly the distal portion of the secondary stent introducer device, is advanced along the wire guide until it is positioned at a first target site in the duct. The primary stent introducer device is advanced distally through the outer introducer catheter, past the side port, and into engagement with the second stent. The second stent is then positioned and deployed at the first target site by retracting the outer introducer catheter proximally relative to the primary stent introducer device, which acts as a pusher for the second stent, to expose the second stent from the distal end thereof.
Once the second stent has been deployed, the primary stent introducer device is advance distally relative to the outer introducer catheter until the first stent is positioned beyond the distal end of the outer introducer catheter. The first stent is then positioned and deployed at the second target site within the duct by retracting the inner introducer catheter proximally relative to the pusher member to expose the stent from the distal end thereof. The entire stent introducer apparatus may then be retracted and removed from the patient.
These and other advantages, as well as the invention itself, will become apparent in the details of construction and operation as more fully described below. Moreover, it should be appreciated that several aspects of the invention can be used with other types of stent delivery catheters or medical devices.
Turning now to
The secondary stent introducer device 14 includes a second self-expanding stent 22 mounted within an outer introducer catheter 24. The outer introducer catheter 24, when disposed about the second stent 22, maintains the second stent 22 in a compressed pre-deployment state. The outer introducer catheter 24 is slidably disposed about the inner introducer catheter 20 of the primary stent introducer device 12. The primary stent introducer device 12 is configured to engage and hold the second stent 22 stationary during movement of the outer introducer catheter 24 relative to the primary stent introducer device 12 and the second stent 22. The second stent 22 is deployed by retracting the outer introducer catheter 24 proximally relative to the primary stent introducer device 12 to thereby expose the second stent 12 from the distal end of the outer introducer catheter 24. Once exposed, the second stent 22 self-expands to its deployed state.
First and second stents 16, 22 each comprise a self-expanding prosthesis, which could include a self-expanding stent, such as the ZILVER™ Biliary Self-Expanding Stent, the SPIRAL Z™ self-expanding stent, and the ZA-STENT™ self-expanding stent, each of which are sold by Wilson-Cook Medical Inc., d/b/a as Cook™ Endoscopy. However, first and second stents 16, 22 could comprise any nitinol, stainless steel, or other self-expanding stent; artificial valve (e.g., venous, heart, pulmonary, etc.) prosthesis, vessel occluder, filter, embolic protection device, shunt, stent graft, etc., that is capable of self-expanding from a compressed pre-deployment (or delivery) state to an expanded deployed state. As such, the term “stent” as used herein refers generally to, but is not limited to, any of the self-expanding devices described above. It is also contemplated that non-expanding stents could also be utilized in the introducer apparatus of the present invention.
In the embodiment illustrated in
In the embodiment illustrated, the support element 32 has a length that will only partially extend into the second stent 22 when the primary stent introducer device 12 is brought into engagement with the second stent 22. However, the support element 32 may have a longer length that is sufficient to extend through the entire second stent 22. This longer length would permit the support element 32 to support the interior of the second stent 22 and prevent the second stent from kinking, buckling or otherwise deforming during its deployment.
The distal end cap 26 further comprises a collar 34 extending proximally from the proximal face of the flange 28. The collar 34 is spaced inwardly from the interior surface 30 of the outer introducer catheter 24 a distance sufficient to accommodate the inner introducer catheter 20 therebetween. In other words, a gap is provided about the exterior surface of the collar 32 that is equal to or larger than the wall thickness of the inner introducer catheter 20. The collar 34 allows the inner introducer catheter 20 to overlap with the distal end cap 26 a distance sufficient to prevent the first stent 16 from being exposed should the inner introducer catheter 20 inadvertently move proximally relative to the pusher member 18 during introduction, advancement and manipulation of the stent introducer apparatus 10. The overlap also provides a seal between the distal end cap 26 and the inner introducer catheter 20 to prevent the first stent 16 from being exposed to bodily fluids or contaminants.
In an alternative embodiment of the invention not illustrated, the outer periphery of distal end cap 26 is completely disposed within the distal end of the inner introducer catheter 20. In this alternative embodiment, and as will be explained in greater detail below, the proximal end of the second stent 22 is engaged by the distal end of the inner introducer catheter 20 during deployment of the second stent 22.
The pusher member 18 further comprises a stent carrying region 36. The stent carrying region 36 is disposed proximally of the distal end cap 26 and comprises a recess having a sufficient depth and length to accommodate the first stent 16 in a compressed pre-deployment state within the interior of the inner introducer catheter 20. In other words, the stent carrying region 36 of the pusher member 18, together with the interior surface 40 of the inner introducer catheter 20, forms a tubular volume within which the first stent 16 is disposed.
The pusher member 18 further comprises a stent pusher 38 disposed adjacent to the proximal end of the stent carrying region 36. The stent pusher 38 is sized to closely but slidably engage with the interior surface 40 of the inner introducer catheter 20. As will be explained in greater detail below, the stent pusher 38 engages the proximal end of the first stent 16 and holds the first stent 16 stationary (relative to the pusher member 18) as the inner introducer catheter 20 is retracted (relative to the pusher member 18) to deploy the first stent 16.
Portions of the distal portion of the pusher member 18 may include barium sulfate or some other agent or marker to provide radiopacity to the primary stent introducer device 12. For example, the distal end cap 26 and the stent pusher 38 can each be made radiopaque so as to enable the user, with the aid of a fluoroscope, to determine the position of the first stent 16 prior to deployment.
The pusher member 18 further comprises an elongate rod 42 extending between the stent pusher 38 and a handle 44 attached to the proximal end of the pusher member 18. The rod 42 is typically, but not necessarily, smaller in cross-section than the interior cross-section of the inner introducer catheter 20 to reduce frictional forces that may be generated by the axial or rotational movement of the pusher member 18 relative to the inner introducer catheter 20. The rod 42 comprises a sufficient rigidity to transmit axial and/or torsional forces between the stent pusher 38 and the handle 44 without excessive bending, buckling or twisting. On the other hand, the rod 42 must be sufficiently flexible to permit passage of the stent introducer apparatus 10 through the patient's bodily lumens. Suitable materials include, but are not limited to, PEEK, polyvinyl chloride (PVC), polyimide, polyimide reinforced with a stainless steel braid, polyurethane, nylon, metal tubing such as nitinol or stainless steel, and the like. The rod 42 may also be formed as a coil or a solid-core wire guide. It should be understood that the rod 42 may be formed integrally with the handle 44 and/or the distal-most portions of the pusher member 18 such as the distal end cap 26, the stent carrying region 36, and the stent pusher 38. In one embodiment, a substantial portion of the rod 42 is formed from nylon tubing while the distal portion, and especially the stent-carrying region, is formed from polyimide.
In the embodiment illustrated, the pusher member 18 comprises a lumen 48 extending through the length of the pusher member 18. The lumen 48 is sized to accommodate a wire guide 50 that may be used to introduce, advance and position the stent introducer apparatus 10 within the patient. For example, and as will be explained in greater detail below, the wire guide 50 may be used to position the secondary stent introducer device 14 within a first leg of a bifurcated duct. The wire guide 50 may then be used to position the primary stent introducer device 12 within the second leg of the bifurcated duct. The lumen 48 may also be used to introduce or remove fluids to or from the target site within the patient. For example, the lumen 48 may be used to inject contrast media into the target site to facilitate fluoroscopic viewing of the area. The handle 44 of the pusher member 18 comprises a fitting or seal 46 that cooperates with a lumen 48. The seal 46 prevents fluids that may enter the distal end of the lumen 48 from passing out through the handle 44 at the proximal end of the lumen 48. The seal 46 comprises a material, or has an adjustable opening, that will accommodate and seal about a wire guide 50 passing therethrough.
The inner introducer catheter 20 generally comprises an elongated tubular structure or sheath made from any suitable material that is sufficiently flexible to permit passage of the stent introducer apparatus 10 through the patient's bodily lumens. The material should also be sufficiently inelastic to resist undue elongation caused by the application of tensile forces at the proximal end of the inner introducer catheter 20 during deployment of the first stent 16. The material may also be made from a clear material such as a substantially clear polymer. Providing a transparency to the inner introducer catheter 20 enables the user to inspect the first stent 16 prior to deployment. Suitable materials include, but are not limited to, polytetrafluoroethylene (PTFE) and polyeretherketone (PEEK).
The inner introducer catheter 20 further comprises a handle 52 attached to the proximal end of the inner introducer catheter 20. The handle 52 attached to the inner introducer catheter 20, in cooperation with the handle 44 attached to the pusher member 18, facilitates movement of the inner introducer catheter 20 relative to the pusher member 18. In particular, and as will be discussed in greater detail below, the user grips and moves handles 44 and 52 towards each other to retract the inner introducer catheter 20 proximally relative to the pusher member 18 to deploy first stent 16. Prior to deployment, handles 44 and 52 are spaced a sufficient distance apart to permit the inner introducer catheter 20 to be moved proximally relative to the pusher member 18 so as to allow the distal end of the inner introducer catheter 20 to be moved proximally of the first stent 16.
The handle 52 of the inner introducer catheter comprises a seal 54 and a fluid injection port 56. The fluid injection port 56 provides a mechanism for flushing the cavity between the inner introducer catheter 20 and the pusher member 18. In particular, a syringe or similar device (not shown) is attached to the fluid injection port 56 and saline is injected therethrough. The saline flushes any air that is trapped within the inner introducer catheter 20 out though the distal end thereof. The seal 54 prevents the saline from escaping out from the proximal end of the handle 52 (about the rod 42) during the flushing procedure.
The outer introducer catheter 24 generally comprises an elongated tubular structure or sheath made from any suitable material that is sufficiently flexible to permit passage of the stent introducer apparatus 10 through the patient's bodily lumens. The material should also be sufficiently inelastic to resist undue elongation caused by the application of tensile forces at the proximal end of the outer introducer catheter 24 during deployment of the second stent 22. The material may also be made from a clear material such as a substantially clear polymer. Providing a transparency to the outer introducer catheter 20 enables the user to inspect the second stent 22, as well as the position of the primary stent introducer device 12, prior to deployment of the second stent 22. Suitable materials include, but are not limited to, polytetrafluoroethylene (PTFE) and polyeretherketone (PEEK).
The outer introducer catheter 24 further comprises a handle 58 attached to the proximal end of the outer introducer catheter 24. The handle 58 attached to the outer introducer catheter 24, in cooperation with the handle 44 attached to the pusher member 18, facilitates movement of the outer introducer catheter 24 relative to the pusher member 18. In particular, and as will be discussed in greater detail below, the user grips and moves handles 44 and 58 towards each other to retract the outer introducer catheter 24 proximally relative to the pusher member 18 to deploy second stent 22. Prior to deployment, handles 44 and 58 are spaced a sufficient distance apart to permit the outer introducer catheter 24 to be moved proximally relative to the pusher member 18 so as to allow the distal end of the outer introducer catheter 24 to be moved proximally of the second stent 22. In addition, it should be understood that the spacing of handles 44 and 58 must also be sufficient to accommodate the handle 52 of the inner introducer catheter 20, which is disposed therebetween.
The distal end 60 of the outer introducer catheter 24 is tapered or rounded to facilitate an atraumatic introduction of the secondary stent introducer device 14 through the patient's bodily lumens. An opening 62 is provided in the distal end 60 to allow the passage of wire guide 50 therethrough. The distal end 60 further comprises weakened areas or slits 64 that allow the distal end to spread apart during deployment of the second stent 22. In particular, slits 64 allow the tapered distal end 60 to spread apart and assume a tubular cross-section substantially equal to the portion of the outer introducer catheter 24 located proximally thereof.
In the embodiment illustrated, the outer introducer catheter 24 comprises a side port 66 through the side wall thereof. The side port 66 is located proximal to the second stent 22, and is preferably located near the proximal end of the second stent 22. However, side port 66 could be spaced away from the proximal end of the second stent 22 by any practical distance. Alternatively, the side port 66 could located distal to the second stent 22, e.g., in or near the tapered end 60. Side port 66 is sized to allow passage of the primary stent introducer device 12 therethrough. In particular, and as will be explained in greater detail below, the primary stent introducer device 12 may be extended out through the side port 66 and positioned within one leg of a bifurcated duct while the secondary stent introducer device 14 is positioned within the other leg of the bifurcated duct. Thus, the side port 66 must be large enough to permit the primary stent introducer device 12 to freely pass therethrough without kinking or excessively bending the primary stent introducer device 12 or the outer introducer catheter 24. In the embodiment illustrated, the side port 66 comprises an elongated opening or slot. The portion of the outer introducer catheter 24 adjacent or surrounding the side port 66 may be reinforced to prevent kinking or excessive bending.
The outer introducer catheter 24 includes radiopaque markers 68 space along the surface thereof. In the embodiment illustrated, one pair of markers 68 are located near the ends of the second stent 22, and another set of markers 68 are located nears the ends of the side port 66. These markers 68 assist the user, with the aid of fluoroscopy, to locate and position the outer introducer catheter 24 during various stages of the stent deployment procedure.
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According to one aspect of the invention, the stent introducer apparatus 10 is used to deploy a self-expanding stent into each of two legs of a bifurcated duct. An exemplary method for performing this procedure is illustrated in
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The distal end of the wire guide 50 is then withdrawn into the distal end of the secondary stent introducer device 14 to a location proximal of the side port 66 in the outer introducer catheter 24. As illustrated in
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According to another aspect of the invention, the stent introducer apparatus 10 is used to deploy two self-expanding stents into a single duct. An exemplary method for performing this procedure is illustrated in
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While there have been described what are presently believed to be the preferred embodiments of the invention, those skilled in the art will realize that changes and modifications may be made thereto without departing from the spirit of the invention. It is to be understood that the invention can be carried out by specifically different equipment and devices, and that various modifications, both as to the equipment details and operating procedures, can be accomplished without departing from the scope of the invention itself.
This application claims the benefit of priority from U.S. Provisional Application No. 60/717,689, filed Sep. 16, 2005, and entitled “Double Metal Stent Introducer”, the contents of which is incorporated herein by reference.
Number | Date | Country | |
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60717689 | Sep 2005 | US |