US20170079762A1 - Method and apparatus for fixation of implantable devices adjacent a body lumen - Google Patents

Abstract

The present application relates to method and apparatus for reducing migration and rotation of implantable devices including an expandable element and an elongate portion.

Description

CLAIM OF PRIORITY
• The present application is a continuation of U.S. patent application Ser. No. 15/143,784, filed May 2, 2016, which is a continuation of U.S. patent application Ser. No. 14/169,988, filed Jan. 31, 2014, which application is a Continuation of U.S. patent application Ser. No. 12/467,257, filed on May 16, 2009, which claims the benefit under 35 U.S.C. 119(e) of U.S. Provisional Patent Application Ser. No. 61/053,758, filed May 16, 2008, which are incorporated herein by reference in their entirety.
FIELD OF THE INVENTION
• The present subject matter relates to method and apparatus for fixation of implantable devices adjacent a body lumen.
BACKGROUND
• The implantation of medical devices into the tissue of patients is complicated. The surgery can be partially or wholly ineffective if the implanted devices migrate or rotate within the body after implantation. Such devices need to be removed and reimplanted if possible. Each time a device is surgically implanted or explanted, the patient suffers risks of trauma and infection, which can sometimes be lethal to the patient.
• There is a need in the art for improved method and apparatus for fixation of implantable devices. Such approaches should provide an explanation option with minimal trauma to the tissue of the patient.
SUMMARY
• The present application relates to method and apparatus for reducing migration and rotation of implantable devices including an expandable element and an elongate portion.
• This Summary is an overview of some of the teachings of the present application and is not intended to be an exclusive or exhaustive treatment of the present subject matter. Further details about the present subject matter are found in the detailed description and the appended claims. The scope of the present invention is defined by the appended claims and their legal equivalents.
BRIEF DESCRIPTION OF THE DRAWINGS
• FIG. 1A shows an example of placement of implantable devices with respect to a human bladder and urethra according to one embodiment of the present subject matter.
• FIG. 1B demonstrates migration of one of the two implantable devices.
• FIG. 1C demonstrates rotation of one expandable element of one of the two implantable devices.
• FIG. 2 shows placement of a sleeve adapted to provide ingrowth to provide an adhesion according to one embodiment of the present subject matter.
• FIG. 3 shows a closeup of the sleeve ofFIG. 2.
• FIG. 4 shows a cross section of an implantable device including a sleeve attached using an adhesive according to one embodiment of the present subject matter.
• FIG. 5 shows a cross section of surface structure adapted to enhance ingrowth according to one embodiment of the present subject matter.
• FIG. 6 shows a cross section of surface structure adapted to enhance ingrowth and resist migration according to one embodiment of the present subject matter.
• FIG. 7 shows a cross section of a helical sleeve structure adapted to enhance ingrowth according to one embodiment of the present subject matter.
• FIG. 8 shows one example of a tool for removal of a helical sleeve structure according to one embodiment of the present subject matter.
• FIG. 9 shows one example of an expandable tool for removal of a helical sleeve structure according to one embodiment of the present subject matter.
• FIG. 10 shows one example of a split ring device adapted to enhance ingrowth according to one embodiment of the present subject matter.
• FIG. 11 shows one example of a segmented ring device adapted to enhance ingrowth according to one embodiment of the present subject matter.
• FIG. 12A shows one example of a hook adapted for fixation according to one embodiment of the present subject matter.
• FIG. 12B shows a cross section of a portion of the implantable device ofFIG. 12A according to one embodiment of the present subject matter.
• FIG. 13 shows one example of a plurality of hooks adapted for fixation according to one embodiment of the present subject matter.
• FIGS. 14A and 14B show one example of use of ingrowth-promoting material at a distal end of an apparatus according to one embodiment of the present subject matter.
• FIGS. 15A to 15E show some examples of an implantable device featuring a variable stiffness design adapted to reduce rotation according to various embodiments of the present subject matter.
• FIG. 16A shows one example of an external stiffener for an implantable device according to one embodiment of the present subject matter.
• FIGS. 16B and 16C show one example of an externally coiled stiffener for an implantable device according to one embodiment of the present subject matter.
• FIGS. 16D and 16E show different examples of an internally coiled stiffener for an implantable device according to various embodiments of the present subject matter.
• FIG. 17 shows one example of a restraint on a proximal bond according to one embodiment of the present subject matter.
• FIG. 18A shows one embodiment of an irregular shape of an expandable element of the implantable device according to one embodiment of the present subject matter, as compared to that ofFIG. 18B.
• FIG. 19 shows one embodiment of a microtextured expandable element according to one embodiment of the present subject matter.
• FIG. 20 shows one embodiment of an extra stabilizing balloon for an implantable device according to one embodiment of the present subject matter.
DETAILED DESCRIPTION
• The following detailed description of the present invention refers to subject matter in the accompanying drawings which show, by way of illustration, specific aspects and embodiments in which the present subject matter may be practiced. These embodiments are described in sufficient detail to enable those skilled in the art to practice the present subject matter. References to “an”, “one”, or “various” embodiments in this disclosure are not necessarily to the same embodiment, and such references contemplate more than one embodiment. The following detailed description is, therefore, not to be taken in a limiting sense, and the scope is defined only by the appended claims, along with the full scope of legal equivalents to which such claims are entitled.
• The present subject matter relates to implantable devices which can be placed near a patient's urethra to improve continence. The implantable devices are described in applications such as such as the implantable devices described in U.S. Pat. Nos. 6,045,498, 5,964,806, 6,579,224, and 6,419,624 and their related patents and applications, the descriptions of which are hereby incorporated in their entirety. Such applications also contain information as to the placement of the implantable devices. Placement of such devices is also discussed in U.S. Provisional Patent Application Ser. No. 61/039,738, filed Mar. 26, 2008, entitled: METHOD AND APPARATUS FOR PLACEMENT OF IMPLANTABLE DEVICE ADJACENT A BODY LUMEN, which is incorporated by reference in its entirety.
• FIG. 1A shows an example of placement of implantable devices with respect to a human bladder and urethra according to one embodiment of the present subject matter. In one embodiment of the implantable devices, anexpandable element10 is connected to anelongate conduit11 and terminates in aport12, such as a septum. Typically, theexpandable element10 is implanted proximal theurethra6 near thebladder5. Such location is also referred to as the “bladder neck.” The actual positions of theexpandable elements10 of such devices with respect to theurethra6 and bladder neck may vary; however,FIG. 1A shows the original position of the devices compared to the positions inFIGS. 1B and 1C for purposes of demonstration of the unwanted aspects of migration and rotation.
• FIG. 1B demonstrates migration of one of the two implantable devices. Some time after implantation, it is possible to find that theexpandable element10 ofimplantable device20 has moved from its original implantation site. In some cases theexpandable element10 will move down the dilation tract formed during implantation of the device. Once it has moved out of position, the implantation may no longer provide adequate tissue bulking in the vicinity of the bladder neck, and may fail to restore continence as needed.
• Another unwanted effect that may be possible to find is rotation.FIG. 1C demonstrates rotation of one expandable element of one of the two implantable devices. Theexpandable element10 ofimplantable device20 is shown as being rotated in position relative to its original placement. The rotation can result in displacement of theexpandable element10, which may reduce the efficacy of the implantation for purposes of enhancing coaptation, and continence. However, rotation can be problematic even in cases where theexpandable element10 is not substantially displaced because theelongate conduit11 can apply unwanted force on theexpandable element10 and may result in device failure over time due to erosion of material.
• One way to reduce the chances of movement of theexpandable element10 after implantation is to provide a means for adhesion of the implantable device to the tissue in which it is implanted.FIG. 2 shows placement of a sleeve adapted to provide ingrowth to provide an adhesion according to one embodiment of the present subject matter. In one embodiment a small adhesion forms near the end of the tubing closest to theexpandable element10 by the use of an ingrowth collar orsleeve30. Different materials can be used, including but not limited to EPTFE (expanded polytetrafluoroethelene as used in some vascular grafts) to encircle theelongate conduit11 near theexpandable element10. The ingrowth collar orsleeve30 allows the adhesion to form which is a form of fixation of the device to avoid migration and to avoid rotation. Other ingrowth materials may include polypropylene or polyethylene mesh as used for hernia repairs or open cell silicone or polyurethane foams. In various embodiments it is beneficial to use a mesh or foam cell size and/or material and/or surface area selected to make the adhesion of limited strength so that theimplantable device20 can be pulled out without breaking it during removal or causing trauma to surrounding tissue. In one embodiment, theingrowth sleeve30 as designed to have less than a 5 lb. pull strength. Other pull strength limits are possible without departing from the scope of the present subject matter.FIG. 3 shows a closeup of the sleeve ofFIG. 2, which is friction fit or otherwise secured to theelongate conduit11 of theimplantable device20 in various embodiments. In certain embodiments the ingrowth material is bioresorbable so that it fixes the device in place after a short time allowing the surrounding tissue to adapt and stabilize the device but would be resorbed over a longer timeframe and allow the device to be easily removed if need be. One example of a bioresorbable material is polylactic acid.
• In one embodiment, theimplantable device20 can be removed by cutting off the septum, feeding a cylindrical tool over the implantable device, and using the tool to go over the conduit, cutting the adhesion to facilitate removal of the implantable device at a pull strength that is less than what would destroy the implantable device. The cylindrical tool may also have a slot along its length so that it can be fit over and along the conduit so that the part need not be cut off. In various embodiments, the tool can cut between the elongate conduit and the sleeve or the tool can cut the sleeve away from the tissue. One type of tool to accomplish the cutting is the use of a properly positioned beveled blade. Other tools and approaches are possible without departing from the scope of the present subject matter.
• FIG. 4 shows a cross section of animplantable device44 including a sleeve40 attached to elongateconduit11 using an adhesive42 according to one embodiment of the present subject matter. Such sleeves40 provide adequate fixation of theimplantable device44 during its implantation. In such embodiments, the adhesive has a tear strength which is less than the pull strength limit of theimplantable device44. Thus, to remove theimplantable device44, the sleeve40 may stay in place while theglue42 shears as theimplantable device44 is pulled out of the patient. In such embodiments, the split ring or segmented ring sleeves as shown inFIGS. 10 and 11 may be used to allow the withdrawal of the implantable device. This is especially useful for devices where the cross section at theexpandable element10 is greater than the cross section for theelongate conduit11. Other types of split ring sleeves may be used without departing from the scope of the present subject matter.
• FIG. 5 shows a cross section of surface structure adapted to enhance ingrowth according to one embodiment of the present subject matter. The surface structure can be porous and is selected to provide the proper pull strength, yet retain the implantable device in position during its normal use.
• FIG. 6 shows a cross section of surface structure adapted to enhance ingrowth and resist migration according to one embodiment of the present subject matter. The angled nature of the structure forms additional resistance to migrations back down the dialation path.
• FIG. 7 shows a cross section of a helical sleeve structure adapted to enhance ingrowth according to one embodiment of the present subject matter. Thehelical sleeve structure70 over theelongate conduit11 acts to fix the implantable device. To remove the device, it is screwed out of the tissue. In one embodiment a pushwire or other rod is used to withdraw the device. The pushwire or rod can be keyed to facilitate application of torque to withdraw the device. In one embodiment, a structure, such as that shown inFIG. 8, is used to lock the pushwire or rod with a channel or other receiver in the implantable device for withdrawal.FIG. 8 shows one example of a tool for removal of a helical sleeve structure according to one embodiment of the present subject matter.
• In various embodiments a collet-type device, such as the expanding device shown inFIG. 9 is used to withdraw the device.FIG. 9 shows one example of an expandable tool for removal of a helical sleeve structure according to one embodiment of the present subject matter. A remote actuator (not shown) is used to expanddistal ring90 so as to engage with a lumen or other feature of the implantable device which is to be extracted.
• FIG. 12A shows one example of a hook adapted for fixation according to one embodiment of the present subject matter. In one embodiment, after theimplantable device122 is placed in position, aNitinol hook120 is threaded through aninner lumen124 of theelongate conduit11 ofimplantable device122 to serve as a fixation to the local tissue. Other types of hooks may be used without departing from the scope of the present subject matter. The hook is placed near theexpandable element10 of theimplantable device122 to retain it in position.FIG. 12B shows a cross section of elongate conduit showing a cross section ofhook120 in the space of what was theinner lumen124 and anotherinner lumen126 in communication withexpandable element10. In various embodimentsinner lumen126 is connected to a port with a septum (not shown) as described in the various documents incorporated by reference. In various embodimentsinner lumen124 is used with various implantation tools such as a pushrod or other tool to placeimplantable device122 in position. Various inner lumens for implantable devices are described in patent documents, including, but not limited to, U.S. Pat. Nos. 6,045,498, 5,964,806, 6,579,224, and 6,419,624 and their related patents and applications, the descriptions of which are hereby incorporated in their entirety. Such applications also contain information as to the placement of the implantable devices. Placement of devices is discussed in various documents, including, but not limited to U.S. Provisional Patent Application Ser. No. 61/039,738, filed Mar. 26, 2008, entitled: METHOD AND APPARATUS FOR PLACEMENT OF IMPLANTABLE DEVICE ADJACENT A BODY LUMEN, which is incorporated by reference in its entirety.
• FIG. 13 shows one example of a plurality of hooks adapted for fixation according to one embodiment of the present subject matter. In various embodiments, fixation hooks130 at the distal tip are deployed to provide fixation to the tissue after theimplantable device132 is placed in its desired position. In various embodiments, theexpandable element10 is expanded and thehooks130 are recessed to shield bladder from puncturing. Other hook positions, shapes, and numbers are possible without departing from the scope of the present subject matter.
• FIGS. 14A and 14B show one example of use of ingrowth-promoting material at a distal end of an implantable device according to one embodiment of the present subject matter. In various embodiments, a patch or coating of ingrowth-promotingmaterial140 at the distal end of thedevice142 provides adhesion at or near the distal end of thedevice142. Such approaches can reduce migration and rotation ofexpandable element10. In certain embodiments the ingrowth material is bioresorbable so that it fixes the device in place after a short time allowing the surrounding tissue to adapt and stabilize the device but would be resorbed over a longer timeframe and allow the device to be easily removed if need be. One example of a bioresorbable material is polylactic acid. It is understood that various materials, shapes and positions can be used without departing from the scope of the present subject matter.
• FIGS. 15A-E show some examples of an implantable device featuring a variable stiffness design adapted to reduce rotation according to various embodiments of the present subject matter. InFIG. 15A different stiffeners are shown, which may be used individually, or in combination, in various applications.FIG. 15B is a cross sectiondrawing showing stiffener153 which is a form of annular ring with an aperture for fillingexpandable element10.FIG. 15C is a cross section showing a stiffeningmember155.FIG. 15D shows a cross section showing a separate lumen with a stiffeningmember157.FIG. 15E shows a cross section with anannular stiffening member159 placed ininner lumen124. In some embodiments, expansion of theexpandable element10 can also make tubing in central portion stretch and can also have a preferential force on the tubing and may cause it to rotate. In various embodiments a stiffener of varying stiffness can be inserted in a lumen of the elongate conduit to provide more stiffening at the distal end than at the proximal end of theimplantable device150. In one application, astiffener157 is added to a third central lumen of the implantable device after it is deployed into position. In varying embodiments, the stiffening effect is built into the implantable device as it is manufactured. In various embodiments, astiffener159 is placed in thesame lumen124 that is used to position the implantable device. This could be done by the surgeon after removing the pushwire at time of implant. Other types of stiffeners and deployments are possible without departing from the scope of the present subject matter.
• FIG. 16A shows one example of an external stiffener for an implantable device according to one embodiment of the present subject matter. In such embodiments,sleeve162 provides additional stiffness at the proximal bond area ofelongate conduit11 of theexpandable element10. In various embodiments, thesleeve162 continues into theexpandable element10 portion of theelongate conduit11. In various embodiments thesleeve162 is manufactured as an integral portion ofelongate conduit11.
• In various embodiments, a lubricious coating, sleeve, or material can be positioned anywhere along the elongate conduit or about the external stiffener in embodiments which employ a stiffener, or both, to reduce or eliminate wear should theexpandable element10 come in contact with the stiffener and/or the elongate conduit. In such events, the lubricious coating, sleeve, or material would prevent wear of theexpandable element10.
• FIGS. 16B and 16C show one example of an externally coiled stiffener for an implantable device according to one embodiment of the present subject matter. As shown inFIGS. 16B and 16C,coil164 can be placed outside ofelongate conduit11. A coil can also be disposed within theelongate conduit11 as shown ascoil168 inFIGS. 16D and 16E.Coils164 and168 provide additional stiffness to prevent rotation of theexpandable element10 ofimplantable device166.
• FIG. 17 shows one example of a restraint on a proximal bond according to one embodiment of the present subject matter. Therestraint172 on the proximal bond of theexpandable element10 to elongateconduit11 reduces or eliminates wear and/or erosion on the proximal bond. In various embodiments, therestraint172 is a collar that is attached to theimplantable device170. In various embodiments, therestraint172 is generated by one or more additional dips in the coating process that produces theimplantable device170. In various embodiments, the restraint provides asymmetric balloon inflation of theexpandable element10. Other shapes and constraints and asymmetries are possible without departing from the scope of the present subject matter.
• Expandable elements with asymmetrical shapes can be engineered to reduce the possibility of contact with the elongate conduit by the expandable element. For example, the bulge shown in the example ofFIG. 17 is larger at the distal end of the expandable element, which can reduce the tendency of the expandable element to come in contact with the elongate conduit.
• FIG. 18A shows one embodiment of an irregular shape of an expandable element of the implantable device according to one embodiment of the present subject matter, as compared to that ofFIG. 18B. The irregular shape is made squarer than that ofFIG. 18B to avoid rotation. Various different shapes may be used without departing from the scope of the present subject matter.
• FIG. 19 shows one embodiment of a microtextured expandable element according to one embodiment of the present subject matter. A portion of the wall ofexpandable element192 is microtextured194 to reduce rotation. A tool can be employed to remove theexpandable element10.
• FIG. 20 shows one embodiment of an extra stabilizing balloon for an implantable device according to one embodiment of the present subject matter.Balloon202 is placed to prevent the implantable device from migrating, and may avoid rotation by holding the elongate conduit in place and thereby limit theexpandable element10 from rotating.
• It is understood that various combinations of the foregoing aspects of the present subject matter can be combined to provide apparatus having multiple benefits.
• This application is intended to cover adaptations and variations of the present subject matter. It is to be understood that the above description is intended to be illustrative, and not restrictive. The scope of the present subject matter should be determined with reference to the appended claim, along with the full scope of legal equivalents to which the claims are entitled.

Claims (11)

1. (canceled)

2. An implantable device for implantation into tissue adjacent to a body lumen, comprising:

an expandable element connected to an elongate conduit, the elongate conduit adapted to provide for a plurality of lumens comprising a first inner lumen for fluid communication between a first end of the elongate conduit and the expandable element at a second end and a second inner lumen; and

a stiffener to prevent or reduce rotation of the device after implantation.

3. The device ofclaim 2 wherein the stiffener comprises an annular ring with an aperture for filling the expandable element.

4. The device ofclaim 2 wherein the stiffener is in a lumen of the device.

5. The device ofclaim 2 wherein the stiffener is of varying stiffness.

6. The device ofclaim 5 wherein the stiffener provides for more stiffening at the distal end than at the proximal end of the implantable device.

7. The device ofclaim 2 wherein the stiffener is configured to be placed in a third inner lumen of the implantable device.

8. The device ofclaim 2 wherein the stiffener is configured to be placed in the second lumen which second lumen is used to position the implantable device.

9. The device ofclaim 2 wherein the stiffener comprises a coil disposed within the elongate conduit.

10. The device ofclaim 2 wherein the stiffener comprises a coil that is external to the elongate conduit.

11. The device ofclaim 2 wherein the device comprises a material on a surface thereof that is adapted to enhance ingrowth.

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