Helical Tissue Anchor Device and Delivery System
20210401427 ยท 2021-12-30
Inventors
- Kenneth F. BINMOELLER (Rancho Santa Fe, CA, US)
- Matthew Thomas Yurek (San Diego, CA, US)
- Michael P. Hartsfield (Poway, CA, US)
- John Greelis (Carlsbad, CO, US)
Cpc classification
A61B2017/0034
HUMAN NECESSITIES
A61B17/0487
HUMAN NECESSITIES
A61B17/0401
HUMAN NECESSITIES
A61B2017/0488
HUMAN NECESSITIES
International classification
A61B17/04
HUMAN NECESSITIES
Abstract
A delivery system for delivering a plurality of helical tissue anchors to repair a wall defect. Coaxially contained within the outer sheath are inner tubular members. The first inner tubular member designed to deploy a first helical tissue anchor, a second inner tubular member designed to deploy a second helical tissue anchor, and a centered inner tubular member contains a cinching mechanism. The two helical tissue anchors are connected to a suture or strap that pull the two helical tissue anchors together to close a tissue defect. A cinching mechanism holds the anchors and tissue defect together and cut the suture or strap.
Claims
1. A multiple helical device and delivery system for repairing wall defects, plicating tissue, and treating lesions comprising the steps of: accessing and visualizing the treatment area using standard endoscopes; advancing the tissue helical anchor through the working channel of the endoscope; attaching a first tissue helical anchor to one side of the treatment site by advancing a forward motion mechanism to advance the first tissue helical anchor and its delivery catheter out of the distal end of the catheter shaft; operating and manipulating the endoscope with the first tissue helical anchor and its delivery catheter to engage the first tissue helical anchor against the first target site; embedding said first tissue helical anchor into the mucosal, submucosal or muscle tissue; releasing the first tissue helical device; retracting said first delivery catheter back into the sheath; engaging the other side of the tissue site by advancing the second tissue helical and its delivery catheter out of the distal end of the catheter sheath; operating and manipulating the scope and second tissue helical anchor and its delivery catheter to engage the second tissue helical anchor against the second target site; embedding the second tissue helical anchor into the mucosal, submucosal or muscle tissue; releasing said tissue second helical anchor; retracting said second delivery catheter back into the sheath; sliding the central tube forward moving the two tissue helical anchors together thus, partially or fully closing the treatment area; and holding the central tube forward and pulling back on the central mandrel lock which cuts the strap or suture into cinching member, Ferrell, bolo tie, spring or anchor.
2. A multiple helical anchor device and delivery system for repairing wall defects, plicating tissue, and treating lesions as recited in claim 1 further comprising the step of adjusting the depth of tissue capture when embedding said first and/or second helical anchol.
3. A multiple helical anchor device and delivery system for repairing wall defects, plicating tissue, and treating lesions wherein as recited in claim 2, further comprising adjusting the depth of tissue capture enabling both full-thickness tissue closure and full-thickness plication.
4. A multiple tissue anchor and delivery system for repairing wall defects, plicating tissue, and treating lesions comprising the steps of: accessing and visualizing the treatment area using standard endoscopy; advancing the helical anchor device through the working channel of the endoscope; engaging one side of the treatment site, advancing one of the thumb slides forward, and advancing the first helical anchor and its delivery catheter out of the distal end of the catheter shaft; manipulating the scope and first helical anchor device and its delivery catheter to position the helical device against the first attachment target site; rotating a first thumbwheel to embed the first helical anchor device into the mucosal or muscle tissue as desired; pulling back on the first release mechanism to release the first helical anchor device. pushing the central button on the first thumb slide down to release the thumb slide allowing it to be pulled proximally; retracting the first thumb slide back, pulling the delivery catheter back into the helical device sheath lumen and leaving the first helical anchor device embedded into the tissue; engaging the other side of the lesion, advance the second thumb slide forward, and advancing the second helical anchor device and its delivery catheter out of the distal end of the catheter shaft; manipulating the scope and second helical anchor device and its delivery catheter to position the second helical anchor device against the second attachment target site; advancing the sheath forward to move the first and second helical anchors together, thus partially or fully closing the tissue defect; pulling or advancing a cinching mechanism to lock the suture holding the first and second helical anchors and tissue walls in the partially or fully closed position; and cutting the suture and releasing the cinching mechanism.
5. A multiple tissue anchor and delivery system for repairing wall defects, plicating tissue, and treating lesions, as recited in claim 4 further comprising the step of adjusting the depth of the tissue capture when embedding said first and/or second helical anchor.
6. A multiple tissue anchor and delivery system for repairing wall defects, plicating tissue, and treating lesions, as recited in claim 5, further comprising that adjusting the depth of tissue capture enable both full-thickness tissue closure and full-thickness plication.
Description
BRIEF DESCRIPTION OF THE DRAWINGS
[0022]
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[0030]
[0031]
[0032] Corresponding reference characters indicate corresponding parts throughout the several views. The exemplifications set out herein illustrate exemplary embodiments of the invention, and such exemplifications are not to be construed as limiting the scope of the invention in any manner.
DESCRIPTION OF THE PREFERRED EMBODIMENTS
[0033] Referring now to the drawings and particularly to
[0034] The multi-lumen catheter can be fabricated from a number of polymeric materials, such as polytetrafluoroethylene (PTFE), FEP, ETFE, polyvinyl chloride (PVC), polyethylene, polypropylene, PEEK, polybutylene, acryaontirile-butadiene-styrene (ABS), rubber modified styrene, polyacetal, polyethylene, graphite or nylon, or a combination of metal coil or braid encapsulated in the polymeric materials or any combination thereof. The diameter of the first inner tubular lumen 13 and the second inner tubular lumen 15 is in the range of 0.25 mm to 1.2 mm, with a preferred diameter of 0.5 mm. The multi-lumen catheter 11 can have a length in the range of 100 to 500 cm depending on the clinical application.
[0035] Now referring to
[0036] Attached to the distal end of the first removable anchor engagement member is first helical tissue anchor 26. First helical tissue anchor 26 has two different winds or thread pitch where the coils are in a tight configuration 36 on the proximal end and have a relatively loose configuration 40 on its distal end. The relatively loose configuration 40 is designed to utilize rotational forces to embed the first helical tissue anchor 26 into the mucosal, submucosal or muscle tissues. It is anticipated by the Applicants that the tight configuration 46 can be appropriately shortened in length to minimize this tight configuration from protruding from the treated tissue area. Also, the depth of tissue anchor capture can be adjusted when embedding the first tissue helical anchor to enable full-thickness tissue closure and full-thickness plication. Located between the first helical tissue anchor 26 and the first removable anchor engagement member 14 is a suture connection area 21 whereby a suture strap mechanism 22 is affixed by a series of rotations around the suture connected area 21. The suture mechanism strap mechanism 22 is designed to allow proximal section of first helical tissue anchor shaft 114, first connector member 12, first removable anchor coupler member 14 and first helical tissue anchor 26 to rotate without the suture strap mechanism rotating. The diameter of the first connection member 12 and the first removable anchor coupler member is in the range of 0.25 mm to 1.2 mm, with a preferred diameter of 0.5 mm. First fixed engagement member 12 and first removable anchor engagement member 14 can be fabricated from metallic materials such as brass, brass alloys, stainless steel, cobalt chrome alloys, nickel titanium, copper alloys or polymer suture materials both resorbable and non-resorbable, such as nylon, polypropylene, polyethylene, Kevlar, polyurethane, lactic acid, polycaprolactone, or metallic materials such as brass, brass alloys, stainless steel, cobalt chrome alloys, nickel titanium, copper alloys or any combination thereof, or any combination thereof or polymeric materials, such as polyvinyl chloride (PVC), polyethylene, polypropylene, PEEK, Ultem, polybutylene, acryaontirile-butadiene-styrene (ABS), rubber modified styrene, polyacetal, polyethylene, graphite, polyurethane or nylon, or any combination thereof.
[0037] The suture strap mechanism 22 can be a mono-strand or multi-strand configuration and can be fabricated from a number of polymer suture materials both resorbable and non-resorbable, such as nylon, polypropylene, polyethylene, Kevlar, polyurethane, lactic acid, polycaprolactone, or metallic materials such as brass, brass alloys, stainless steel, cobalt chrome alloys, nickel titanium, copper alloys or any combination thereof, or any combination thereof or polymeric materials, such as polyvinyl chloride (PVC), polyethylene, polypropylene, PEEK, polybutylene, acryaontirile-butadiene-styrene (ABS), rubber modified styrene, polyacetal, polyethylene, graphite, polyurethane or nylon, or any combination thereof.
[0038] Also shown in
[0039] Now referring to
[0040] Attached to the distal end of the second removable anchor engagement member is second helical tissue anchor 42. Second helical tissue anchor 42 has two different winds or thread pitch where the coils are in a tight configuration 46 on the proximal end and have a relatively loose configuration 44 on its distal end. The relatively loose configuration 44 is designed to utilize rotational forces to embed the second helical anchor 42 into the mucosal, submucosal or muscle tissues. It is anticipated by the Applicants that the tight configuration 46 can be appropriately shortened in length to minimize this tight configuration from protruding from the treated tissue area. Also, the depth of tissue capture can be adjusted when embedding the second helical tissue anchor to enable full-thickness tissue closure and full-thickness plication. Located between the second helical tissue anchor 42 and the second removable anchor engagement member 16 is a second suture connection area 23 whereby a suture strap mechanism 22 is affixed by a series of rotations around the second suture connected area 23. The suture mechanism strap mechanism 22 is designed to allow proximal section of second tissue anchor shaft 116, second connector member 29, second removable anchor coupler member 16 and second helical tissue anchor 42 to rotate without the suture strap mechanism rotating. Second fixed engagement member 29 and second removable anchor engagement member 16 can be fabricated from metallic materials such as brass, brass alloys, stainless steel, cobalt chrome alloys, nickel titanium, copper alloys or polymer suture materials both resorbable and non-resorbable, such as nylon, polypropylene, polyethylene, Kevlar, polyurethane, lactic acid, polycaprolactone, or metallic materials such as brass, brass alloys, stainless steel, cobalt chrome alloys, nickel titanium, copper alloys or any combination thereof, or any combination thereof or polymeric materials, such as polyvinyl chloride (PVC), polyethylene, polypropylene, PEEK, polybutylene, acryaontirile-butadiene-styrene (ABS), rubber modified styrene, polyacetal, polyethylene, graphite, polyurethane or nylon, or any combination thereof.
[0041] Also shown in
[0042] Now referring to
[0043] Shown in the perspective view of
[0044] In
[0045]
[0046] The first inner tubular member 114, at the sheath strain relief 100, enters the handle body 78 from its originating distal end whereby the outer surface of the first inner tubular member 114 is engaged to the first thumbwheel 96 allowing for rotational movement and embedment of the first helical tissue anchor 26. The first inner tubular member 114 is further engaged to the first slide mechanism 88 for advancing and retracting the first tubular member 114 within the sheath and for maneuvering its proximal end with first helical tissue anchor 26, towards the desired treatment site. The first release button 84 is also engaged to the first inner tubular member's stylus for releasing the first helical tissue anchor 26 after embedment in the tissue.
[0047] The second inner tubular member 116, at the sheath strain relief, 100 enters the handle body 78 from its distal end whereby the outer surface of the second inner tubular member 116 is engaged to the second thumbwheel 94 allowing for rotational movement for embedment of the second helical tissue anchor 42. The second inner tubular member 116 is further engaged to the second slide mechanism 90 for advancing and retracting the second tubular member 116 within the sheath and for maneuvering its proximal end with second helical tissue anchor 42, towards the desired treatment site. The second release button 86 is also engaged to the second inner tubular member's stylus for releasing the second helical tissue anchor 42 after embedment in the tissue.
[0048] The handle body 78, the pair of thumbwheels 94, 96, the pair of slide buttons 86, 88 and the pair or release buttons 84, 86 all can be fabricated from a number of polymeric materials, such as polyvinyl chloride (PVC), polyethylene, polypropylene, PEEK, polybutylene, acryaontirile-butadiene-styrene (ABS), rubber modified styrene, polyacetal, polyethylene, polyurethane or nylon, or any combination thereof.
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[0052] The Applicants anticipate that further developments and embodiments for a tissue anchor and delivery device with multiple tissue anchors in series within a catheter including a specifically designed apparatus to deploy series of anchors (details not shown in the Figures). In this additional embodiment, the tissue anchor(s) are deployed within the catheter in an extended or flat like form, then as they are pushed out of a constraining tube they immediately curl into a circular or helical-like configuration. Further modifications or embodiments for the tissue anchor device has at least two tissue anchors arranged in series within a catheter with a suture or suture like material affixed to the first or distal anchor then threaded through the eyelets of each following anchor(s). The suture is allowed to slide freely through the following anchors then the suture extends through the catheter and out the proximal end of the catheter such that the operator can grasp the end of the suture. A sliding crimp tie is positioned between every two anchors in series along the catheter. Once the first anchor is fired and affixed to tissue it exits the catheter, suture attached, moving the second anchor, with sliding but attached suture to the forward or distal end of the catheter. Once the second anchor is affixed to tissue the suture material connects these two affixed anchors and a sliding crimp tie also exits the catheter following the second anchor. The operator grasps the proximal suture end and pulls it with the crimp tie supported by the distal end of the catheter and slides the tie such that the anchors become close to each other and fixed in this configuration, whereby a defect would be closed. Two, three, four, or any number of anchors can be deployed in the same manner as described above to close a complex tissue defect.
[0053] Operation
[0054] The Operation Steps of the first embodiment for repairing wall defects and lesions are presented below.
[0055] Access and visualize the treatment area using standard endoscopy.
[0056] Advance the helical tissue anchor device through the working channel of the endoscope.
[0057] To engage one side of the treatment site, advance one of the thumb slides forward advancing and locking the first helical device and its delivery catheter out of the distal end of the catheter shaft at a desired length. The first helical device and its delivery catheter can be visualized by the endoscope.
[0058] Manipulate the scope and first tissue helical anchor and its delivery catheter to position the first tissue helical device against the first attachment target site.
[0059] Rotate a first thumbwheel to embed the first tissue helical device into the mucosal, submucosal or muscle tissue as desired.
[0060] Pull back on the first release mechanism to release the first helical device.
[0061] Push the central button on the first thumb slide to release the thumb slide allowing it to be pulled proximally.
[0062] Retract the thumb slide back, pulling the delivery catheter back into the sheath of the helical device leaving the first helical device attached to the suture strap mechanism embedded into the tissue.
[0063] To engage the other side of the lesion, advance and lock the second thumb slide forward advancing the second helical tissue anchor and its delivery catheter out of the distal end of the catheter shaft at a desired length. The second helical tissue device and its delivery catheter can be visualized by the endoscope.
[0064] Manipulate the scope and second helical tissue anchor and its delivery catheter to position the second tissue helical device against the second attachment target site.
[0065] Rotate the other thumbwheel to embed the second tissue helical device into the mucosal, submucosal, or muscle tissue as desired.
[0066] Pull back on the second release mechanism to release the second tissue helical device.
[0067] Push the central button on the second thumb slide down to release the thumb slide allowing it to be pulled proximally.
[0068] Retract the thumb slide back, pulling the delivery catheter back into the sheath of the helical device leaving the second tissue helical device attached to the suture strap mechanism embedded into the tissue.
[0069] Advance the entire device forward allowing the tensioned suture strap mechanism to pull the suture strap into outer sheath until the two anchors and the tissue defect walls are pulled together partially or fully closing the tissue defect.
[0070] Pull the proximal retraction finger grips back to initially lock the suture strap into the cinching and excising tubular member.
[0071] Continue to pull on the retraction finger grips to cut the suture strap and release the suture cinching and excising inner tubular member from the cinching member.
[0072] The device can then be removed from the endoscope leaving the tissue defect partially or fully closed by the cinched anchors.
[0073] In another embodiment of the device, the cinching mechanism could be a separate catheter. In this embodiment, the device is removed from the endoscope once the anchors are placed leaving suture strap mechanism in the endoscope channel.
[0074] By holding the central mandrel fixed and sliding the separate cinching device forward, a cinch, ferrell, bolo tie or spring or knot pushed with a knot pusher is pushed distally moving and locking the two helical anchors together thus, partially or fully closing the treatment area.
[0075] While this invention has been described as having a preferred design, the present invention can be further modified within the spirit and scope of this disclosure. The application is therefore intended to cover any variations, uses, or adaptations of the invention using its general principles. Further, this application is intended to cover such departures from the present disclosure as come within known or customary practice and the art to which this invention pertains and which fall within the limits of the appended claims.