US20050203550A1 - Surgical fastener - Google Patents
Surgical fastener Download PDFInfo
- Publication number
- US20050203550A1 US20050203550A1 US10/798,465 US79846504A US2005203550A1 US 20050203550 A1 US20050203550 A1 US 20050203550A1 US 79846504 A US79846504 A US 79846504A US 2005203550 A1 US2005203550 A1 US 2005203550A1
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- Prior art keywords
- fastener
- surgical fastener
- poly
- state
- anchor
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Classifications
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B17/00—Surgical instruments, devices or methods, e.g. tourniquets
- A61B17/10—Surgical instruments, devices or methods, e.g. tourniquets for applying or removing wound clamps, e.g. containing only one clamp or staple; Wound clamp magazines
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B17/00—Surgical instruments, devices or methods, e.g. tourniquets
- A61B2017/00004—(bio)absorbable, (bio)resorbable, resorptive
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B17/00—Surgical instruments, devices or methods, e.g. tourniquets
- A61B17/00234—Surgical instruments, devices or methods, e.g. tourniquets for minimally invasive surgery
- A61B2017/00292—Surgical instruments, devices or methods, e.g. tourniquets for minimally invasive surgery mounted on or guided by flexible, e.g. catheter-like, means
- A61B2017/003—Steerable
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B17/00—Surgical instruments, devices or methods, e.g. tourniquets
- A61B2017/00535—Surgical instruments, devices or methods, e.g. tourniquets pneumatically or hydraulically operated
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B17/00—Surgical instruments, devices or methods, e.g. tourniquets
- A61B2017/00831—Material properties
- A61B2017/00858—Material properties high friction, non-slip
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B17/00—Surgical instruments, devices or methods, e.g. tourniquets
- A61B2017/00831—Material properties
- A61B2017/00898—Material properties expandable upon contact with fluid
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B17/00—Surgical instruments, devices or methods, e.g. tourniquets
- A61B17/04—Surgical instruments, devices or methods, e.g. tourniquets for suturing wounds; Holders or packages for needles or suture materials
- A61B17/0401—Suture anchors, buttons or pledgets, i.e. means for attaching sutures to bone, cartilage or soft tissue; Instruments for applying or removing suture anchors
- A61B2017/0409—Instruments for applying suture anchors
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B17/00—Surgical instruments, devices or methods, e.g. tourniquets
- A61B17/04—Surgical instruments, devices or methods, e.g. tourniquets for suturing wounds; Holders or packages for needles or suture materials
- A61B17/0401—Suture anchors, buttons or pledgets, i.e. means for attaching sutures to bone, cartilage or soft tissue; Instruments for applying or removing suture anchors
- A61B2017/0417—T-fasteners
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B17/00—Surgical instruments, devices or methods, e.g. tourniquets
- A61B17/04—Surgical instruments, devices or methods, e.g. tourniquets for suturing wounds; Holders or packages for needles or suture materials
- A61B17/0401—Suture anchors, buttons or pledgets, i.e. means for attaching sutures to bone, cartilage or soft tissue; Instruments for applying or removing suture anchors
- A61B2017/0419—H-fasteners
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B17/00—Surgical instruments, devices or methods, e.g. tourniquets
- A61B17/04—Surgical instruments, devices or methods, e.g. tourniquets for suturing wounds; Holders or packages for needles or suture materials
- A61B17/0401—Suture anchors, buttons or pledgets, i.e. means for attaching sutures to bone, cartilage or soft tissue; Instruments for applying or removing suture anchors
- A61B2017/044—Suture anchors, buttons or pledgets, i.e. means for attaching sutures to bone, cartilage or soft tissue; Instruments for applying or removing suture anchors with a threaded shaft, e.g. screws
- A61B2017/0443—Suture anchors, buttons or pledgets, i.e. means for attaching sutures to bone, cartilage or soft tissue; Instruments for applying or removing suture anchors with a threaded shaft, e.g. screws the shaft being resilient and having a coiled or helical shape in the released state
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B90/00—Instruments, implements or accessories specially adapted for surgery or diagnosis and not covered by any of the groups A61B1/00 - A61B50/00, e.g. for luxation treatment or for protecting wound edges
- A61B90/03—Automatic limiting or abutting means, e.g. for safety
- A61B2090/037—Automatic limiting or abutting means, e.g. for safety with a frangible part, e.g. by reduced diameter
Definitions
- the present invention relates to surgical fasteners and more specifically to surgical fasteners suitable for use in both open procedures, and minimally or less invasive procedures where the operative or surgical site is not directly accessible by the surgeon.
- Surgical fasteners are known to be an alternative to traditional suturing techniques for procedures involving tissue closure, connection, or repair.
- One undesirable aspect of manual suturing is that the suturing process adds time to the overall surgical process.
- manual suturing often requires that the operative area is readily accessible so that the medical practitioner can manipulate the suture and associated needle through both sides of the tissue, connection or repair site.
- surgical fasteners are known to provide a means to close an open surgical incision or wound, hold together pieces of soft tissue, attach devices to tissue, or repair torn tissue in orthopedic/musculoskeletal applications. Such surgical fasteners are often used where there is adequate access to the operative area, or for invasive, open procedures.
- suturing techniques requires considerable skill and dexterity especially when tying knots in the suture or otherwise manipulating the suture.
- the ability of a medical practitioner to manipulate a suture as well as knot the ends of the suture are further complicated when the site is not directly accessible to the practitioner. In such cases, even if the complexity of suturing does not prevent the procedure from being completed in a minimally invasive manner, the length of the procedure is likely to increase.
- the present invention includes a surgical fastener for deployment through a device (such as tubular device, a needle, cannula, catheter, etc.), where the fastener comprises a first anchor member, a second anchor member, and a connecting portion separating the first and second anchor members, where at least the first anchor member and the second anchor member each are expandable from a first state to a second state where the second state is of a larger size than the first state, where the larger size may be achieved by an increase in displacement (e.g., volume, profile, configuration, etc.) of a portion of the fastener or the entire fastener.
- the anchor may change in shape or conform to a profile that is of a larger size than the profile of the first state.
- the increase in volume may be achieved by relaxing a previous state of compression of the fastener portion.
- the fastener portion may comprise a resilient material that is compressible, and/or the fastener portion may be hollow, or have a cavity, such that the outer perimeter of the anchor portion may be folded into the cavity to assume the first state, or compress the cavity to conform to a smaller state.
- the surgical fastener may also comprise a first means for anchoring the fastener, a second means for anchoring the fastener and a connecting portion separating the first and second means for anchoring.
- the means for anchoring may be any of the anchor portions described herein.
- the invention also includes a surgical fastening system comprising, a tubular member having a proximal and distal end and a lumen extending therebetween, the tubular member being sufficiently flexible to navigate tortuous anatomical passages within a human body, a distal portion located at the distal end of the tubular member, the distal portion having a distal tip being configured to pierce tissue, the distal portion having a lumen extending between the tubular member lumen and an opening in the distal portion, at least one surgical fastener slidably located entirely inside the tubular member lumen, where the surgical fastener comprises a first anchor member, a second anchor member, and a connecting portion separating the first and second anchor members, and an advancing member slidably located within the tubular member lumen such that advancement causes a distal portion of the advancing member to advance the surgical fastener through the tubular member.
- a surgical fastening system comprising, a tubular member having a proximal and distal end and a lume
- the system of the present invention may be directed to the desired site using a catheter-guidewire configuration, shaped catheter, a steerable catheter, a scope-type of device (e.g., such as endoscopes, gastroscope, colonoscope, bronchoscope, or any type of scope used to access sites within the body.)
- a scope-type of device e.g., such as endoscopes, gastroscope, colonoscope, bronchoscope, or any type of scope used to access sites within the body.
- the present invention is useful in many surgical procedures requiring fastening systems, including but not limited to, procedures for fastening or repairing tissue or attachment of implant materials to tissue.
- the present invention is suitable for, but not limited to, use in the heart, stomach, gastro-intestinal tract, etc. While the faster and fastening system may be used in open procedures, the devices and systems may also be used in minimally invasive procedures where the operative site is remotely accessed using minimally invasive techniques including catheterization and/or endoscopic or similar means.
- the inventive devices are especially suited for advancement via a minimally invasive technique by providing features which improve the ability of the surgeon to deploy the fastener with accuracy and effectuate a proper seal with the fastener.
- the minimally invasive technique also may allow for visual inspection of the placement of the anchor.
- FIGS. 1A-1B illustrate a side view of a basic variation of a fastener of the present invention.
- FIGS. 2A-2H illustrate additional examples of various fasteners.
- FIGS. 3A-3B illustrate a variation of a fastener having a single diameter (or similar cross-sectional measurement) prior to deployment.
- FIG. 3C illustrates a variation of a fastener having an insert.
- FIGS. 4A-4C illustrate an example of a fastener system deploying a fastener.
- FIGS. 5A-5B illustrate another variation of a fastener system.
- FIG. 6A illustrates a deployed fastener having elastic properties.
- FIGS. 7A-7C illustrate variations of fastening systems of the present invention.
- FIGS. 8A-8F illustrate additional features of fastening systems of the present invention.
- FIGS. 1A-1B illustrate a side view of a basic variation of the inventive fastener 100 .
- the fastener 100 includes a first anchor member 102 and a second anchor member 104 and a connecting portion 106 separating the two anchor members 102 104 .
- the “I-type” fastener shape illustrated in FIGS. 1A-1B is merely for illustrative purposes.
- the anchor portions 102 104 may have a variety of shapes, cross-sections, and configuration as discussed herein.
- the anchor portions 102 104 will generally have a shape that allows for retention of a medium (for example, torn/damaged tissue, two or more discrete pieces of tissues, one or more implants to tissue, a combination thereof, etc.) between the anchor portions 102 104 upon deployment of the anchor 100 .
- Portion(s) of the fastener 100 will be operable between a first and second state where in the second state, a portion or portions of the fastener 100 will be of a larger size and/or profile than the first state.
- the fastener 100 anchors 102 104 are configured so that they expand from the first state, shown in FIG. 1A , to a larger second state.
- the fastener 100 may be delivered to the operative site when the portions of the fastener 100 are in the first state. Upon deployment, selected portions of the fastener 100 assume the larger second state. This configuration allows for delivery of the fastener 100 through an opening in the medium where the opening is smaller than a diameter (or other similar dimension) of the fastener 100 portions after deployment.
- construction of the fastener 100 allows only a portion (e.g., a single anchor, both anchors, the connecting portion, or a combination thereof) to expand into the second state.
- the entire fastener 100 may be constructed to assume the second state upon deployment. It is contemplated, that the various portions of the fastener 100 may expand differently as required for the particular application (e.g., one or more portions expand at a different rate, a different size, etc.)
- the fastener 100 may be constructed of a shape or material that allows compression of the fastener portion, either by application of a compressive force or application of a vacuum, etc.
- the fastener 100 may include a material that swells or expands given the addition of a fluid (e.g., natural body fluids or fluids introduced during the surgical procedure.)
- biodegradeable and non-biodegradeable polymers examples include biodegradeable and non-biodegradeable polymers, elastomers, shape-memory alloys, other alloys, etc.
- carbonate copolymer polyether ester copolymer, albumin, gelatin, starch, cellulose, dextrans, polysaccharides, fibrinogen, poly (D,L lactide), poly (D,L-lactide-co-glycolide), poly (glycolide), poly (hydroxybutyrate), poly (alkylcarbonate) and poly (orthoesters), EVA copolymers, silicone rubber and poly (methylmethacrylate).
- Particularly preferred polymeric carriers include poly (ethylene-vinyl acetate), poly (D,L-lactic acid) oligomers and polymers, poly (L-lactic acid) oligomers and polymers, poly (glycolic acid), copolymers of lactic acid and glycolic acid, poly (caprolactone), poly (valerolactone), polyanhydrides, copolymers of poly (caprolactone) or poly (lactic acid) with polyethylene glycol, PET, PETE, and blends thereof.
- the second state of the fastener comprises a larger profile or configuration as compared to the first state. As stated above, this permits securing of the anchoring portions 102 104 about the medium and/or securing of the connecting portion 106 within the medium.
- Another advantage of the invention is that the opening in the medium created during deployment of the fastener 100 may be smaller than would otherwise be possible if the fastener did not expand into the second state upon or after deployment.
- the fastener may incorporate a variety of additives, coatings, adjuncts, etc.
- the fastener (or only portions of the fastener) may include a lubricious coating to improve advancement of the fastener in the delivery system.
- the fastener may include non-proliferative drugs, thrombogenic additives, non-thrombogenic additives, non-inflammatory medicines, additives to induce fibrosis for wound closure, anti-platelet, anti-coagulent, growth factors, gene-transductors, cell matrix, glue, cement, protein, hydrophilic, hydrophobic, lipidphillic, lipidphobic, or combinations where appropriate.
- FIGS. 2A-2H illustrate examples of various fasteners 100 of the present invention. It should be understood that the fasteners 100 of the present invention may have a number of configurations as required for the specific application. These figures are intended to illustrate some possible variations of the invention. As noted herein, where possible, combinations of features of various embodiments and the embodiments themselves are within the scope of the invention.
- FIG. 2A illustrates a fastener 100 similar to that shown in FIGS. 1A-1B .
- FIG. 2B illustrates a variation of the fastener 100 where the anchor portions 102 104 have a spherical shape.
- the anchor portions 102 104 are illustrated as having a cavity 108 .
- the cavity 108 may assist in reducing the size of the anchor portions 102 104 into the first state.
- the cavity 108 (as well as other portions of the fastener 100 ) may serve as a reservoir for various medications, drugs, etc.
- variations of fasteners of the present invention may be non-porous if the particular application requires (e.g., where prevention of tissue in-growth is required. Alternatively, variations of the fastener may be porous.
- the fastener may be selected such that certain portions of the fastener are porous while others are non-porous (e.g., porous anchor members combined with a non-porous connecting member, non-porous anchors with a porous connecting member, etc.)
- porous materials may be selected for construction of the anchor or non-porous materials may be altered to contain pores.
- FIG. 2C illustrates another variation of the fastener 100 in which the anchor portions 102 104 comprise cross-shaped members.
- FIG. 2D illustrates a fastener 100 having anchor portions 102 104 that are planar-disc-shaped. In such a configuration, the increased surface area of the anchor portions 102 104 may provide better contact between the fastener 100 and the medium to allow for tissue in-growth or for delivery of a therapeutic substance carried by the fastener 100 .
- FIG. 2E illustrates a variation of a fastener 100 of the present invention where the first anchor portion 102 and the second anchor portion 104 comprise different shapes. It should be noted that variations of the invention include fasteners 100 having combinations of anchor portions as illustrated herein or variations thereof.
- FIG. 2F illustrates a variation of a fastener 100 of the present invention where the first anchor portion 102 and the second anchor portion 104 extend in different directions.
- FIG. 2G illustrates a variation of the fastener 100 of the present invention where the anchor portions 102 and 104 comprise “pig-tail” type fasteners.
- the anchor portions 102 and 104 the coils of the pig-tail may separate to capture tissue therebetween.
- the opposing anchor portions 102 and 104 may be used to capture the tissue.
- the pig-tail anchors may be straightened in the device for delivery.
- the coils may be compressed in a radial dimension to expand upon deployment from the delivery system.
- a variation of a pig-tail fastener may include a helical shaped fastener or fastener with helical anchor portions.
- FIG. 2H illustrates another variation of the invention where a fastener 100 includes protrusions 112 .
- the protrusions 112 may assist in retaining the anchors and or fastener in the deployment site.
- the protrusions 112 may comprise bio-active substances as described herein.
- the figure illustrates the protrusions as on the anchor portions only, the invention includes fasteners 100 having protrusions 112 on the connecting portion 106 as well.
- the protrusions 112 may be located only on the connecting portion 106 .
- anchor portions described herein may be configured/suited for attachment of external devices/implants/objects/etc.
- one possible use of the inventive fastener is placing the fastener in the wall of an organ, then attaching an implant to the organ's wall by attaching the implant to the anchor portions of the fastener.
- FIGS. 3A-3B illustrate another variation of a fastener 100 of the present invention.
- the anchor portions 102 104 in the pre-deployment or first state, have substantially the same cross sectional measurement as the connecting portion 106 .
- the anchor portions 102 104 when the anchor portions 102 104 assume the second state, they expand to a greater size than the connecting portion 106 .
- the anchor portions 102 104 may be constructed from a material similar to that of the connecting portion 106 but having different additives or structure to allow for expansion into the second state.
- portions of the fastener 100 may be formed from different materials and joined, or molded together to form the composite fastener.
- FIG. 3C illustrates another variation of a fastener 100 of the present invention.
- the fastener 100 includes an insert 110 .
- the insert 110 may comprise a bioabsorbable material which dissolves/ is absorbed by the body at a slower rate than the remainder of the fastener 100 .
- the insert 110 may be a nonbiodegradeable/non-bioabsorable material such that as tissue replaces the absorbable fastener material, the insert remains to provide long term retention of tissue.
- the insert 110 may comprise a metallic material to provide a radiopaque marker for placement, or for subsequent location of the fastening site. Such a combination may be used with absorbable and non-absorbable fasteners.
- the insert 110 illustrated in FIG. 3C comprises end portions having a larger dimension than the center portion, the invention is not limited as such.
- FIGS. 4A-4C illustrate a basic example of a system 150 which deploys fasteners 100 of the present invention.
- the system 150 includes a tubular member 152 that is sufficiently flexible so that it may navigate tortuous passages to access the surgical site yet it will have sufficient column strength so that it may penetrate tissue to deploy the fastener 100 .
- variations of the tubular member 152 may be reinforced to minimize kinking of the tubular member as it navigates toward the surgical site.
- the tubular member 152 retains a fastener 100 in a lumen 154 that extends between a proximal and distal end of the tubular member 152 .
- the fastener 100 is slidably located inside the tubular member 152 and may be advanced using an advancing member 156 that is also slidably located within the tubular member lumen 154 .
- the advancing member may simply push the fastener using a linear or rotary type drive system.
- the advancing member may be an auger type system that advances the fastener with the assistance of rotatable vanes within the tubular member.
- a pneumatic, hydraulic, or fluid filled actuation may also be used to advance/retract the advancing member.
- the advancing member 156 may be a guidewire or other similar type device that is able to deploy the fastener 100 at the operative site.
- the fastener 100 may be removably attached to the advancing member 156 to improve accuracy in deployment of the fastener 100 .
- the fastener 100 is configured relative to the lumen 154 so that friction retains the fastener 100 within the lumen 154 until deployment of the fastener 100 .
- the wall surface and/or diameter of the lumen 154 may be selected to increase the sliding resistance of the fastener 100 .
- the system will be configured so that upon deployment of the first anchor the fastener 100 will release from the device rather than pulling out of the tissue.
- the system 150 also includes a distal portion 158 located at the distal end of the system 150 .
- the distal portion 158 has a distal tip 160 configured to pierce tissue and has an opening 162 through which the fastener 100 exits the device.
- the distal tip 160 is configured to prevent “coring” of the tissue to minimize the size of any opening created during deployment of the fastener.
- the tip 160 configuration has a sharpened area and a taper proximal to the sharpened area so that the tip 160 makes a small puncture and then dilates the opening in the tissue.
- FIG. 4B illustrates the system 150 of FIG. 4A after the distal portion 158 advances through two layers of tissue 1 and 2 and one anchor portion 102 exits from the system 150 .
- the fastener 100 may expand upon exiting the system 150 via being released from the constraint of the system 150 .
- fluids may cause the fastener 100 to increase in size. Such fluids may be introduced during the procedure or may be naturally occurring at the operative site. Therefore, the fastener 100 may expands to a size greater than the opening in tissue that is created by the fastening system 150 .
- the distal portion 158 and tubular member 152 are retracted through the tissue 1 . Once retracted, the system 150 deploys the second anchor portion (not illustrated) thereby retaining the tissues 1 between the anchor portions 102 104 .
- FIG. 4C illustrates the system 150 of FIGS. 4A and 4B after the distal portion 158 is withdrawn through the tissue 1 sufficiently enough so that the opening 162 is on the near side of the tissue 1 . Once in the appropriate position, the device 150 deploys the remaining anchor portion 104 .
- the system illustrated in FIGS. 4A-4C is depicted to show a basic variation of the invention. It is contemplated that the invention includes variations configured to first deploy an anchor portion on a near side of the tissue (e.g., prior to insertion of the distal tip into the tissue), then advance the distal tip into the tissue to deploy the remaining anchor portion on the far side of the tissue.
- the fastener of the present invention may be delivered through any tubular device such as a cannula, a catheter, polymeric tubing, etc.
- the fastener may be part of a fastening system that permits deployment of the fastener in remote parts of the body through a variety of minimally invasive procedures.
- the system may include a steerable catheter, or the system may be guided to the site via a separate catheter, a separate steerable catheter, a endoscope-type device, pre-shaped catheter, etc.
- FIGS. 5A-5B illustrate another variation of a system 150 of the present invention.
- the opening 162 is located at a distal end of the device rather than in a side-wall of the distal portion.
- the fastener 100 may be located immediately adjacent the opening 162 to prevent the coring of tissue as the distal tip 160 advances through tissue.
- FIG. 5B illustrates a sectional view taken along the line 5 B- 5 B of FIG. 5A .
- the system 150 may include a lumen that is appropriately shaped to orient the anchor and central portions of the fastener 100 .
- the lumen may be extruded to form a channel for the central portion.
- the system may include a multi- lumen design to allow for fluid delivery ports 164 if required.
- the fastener 100 portions upon deployment of the fastener 100 from the system 150 , the fastener 100 portions shall increase in size from the first state to a second state where the larger size may be achieved by an increase in volume and/or profile a portion of the fastener or the entire fastener.
- the invention contemplates that the fastening delivery system 150 may be used to constrain the fastener 100 into the first state, via a compression mechanism.
- the fastener 100 or portions of the fastener may be configured to increase in size given the application of a fluid.
- the fluid may comprise naturally occurring bodily fluid or fluid delivered by the fastening system or even fluid delivered via a separate device.
- one of the functions of the inventive tissue fastener is to retain two pieces of tissue together, retain an implant to the tissue, or close an opening in tissue.
- the feature of the inventive fastener 100 relating to expansion of the anchor portions 102 104 permits placement of the fastener 100 using an opening in the tissue that is smaller would otherwise be required.
- fasteners of the present invention may also be configured such that the central portion 106 expands into a second state as well. In such variations, expansion of the center portion may allow for expedited healing of the opening in tissue, or for closure and sealing of the opening in the tissue.
- the central portion 106 may be configured from a material that allows stretching of the center portion 106 during deployment. As shown in FIG.
- such a fastener 100 having elastic properties allows for an increased compressive force on the medium being retained between the fastener.
- An additional benefit of such an elastic fastener is that the length of the fastener 100 (e.g., as measured in a direction along the central portion) can accommodate a greater range of tissue and/or material thicknesses.
- FIG. 7A illustrates a variation of a fastening system 150 of the present invention.
- the system 150 depicts a single fastener 100 located within the device, it is contemplated that the system 150 may comprise a number of fasteners 100 to permit serial deployment during use of the system.
- the system 150 includes a flexible tubular member 152 extending between having proximal and distal ends and a lumen extending between the ends.
- the system 150 includes a distal portion 158 the distal end of the tubular member 152 .
- the distal portion 158 may comprise a separate material or insert that is coupled to the tubular member 152 .
- the distal portion 158 may be formed from the same material as the tubular member 152 .
- the distal portion 158 includes a distal tip 160 for penetrating tissue (and/or an implant, etc.).
- the distal portion 158 includes a lumen that is in fluid communication with a lumen of the tubular member 152 .
- the distal portion 158 also includes an opening 162 through which the fastener 100 deploys.
- the opening 162 is located in a side wall of the distal portion 158 .
- the opening may be at the distal tip 160 .
- the tubular member 152 will have sufficient column strength to allow for penetration of tissue via advancement of the system 150 .
- the tubular member 152 may be constructed of a material that provides sufficient flexibility and column strength.
- the tubular member 152 may include a reinforcing member 166 , such as a coil, braid, or fiber reinforcement.
- the system 150 includes an advancing member 156 that permits advancement and/or deployment of the fastener 100 .
- the tubular member and/or advancing member may be selected from materials that minimize the friction between the two members. Alternatively, or in combination, these items may include a lubricious coating to minimize friction.
- the system 150 may include an additional fluid delivery means, such as a fluid source where delivery of the fluid occurs via the lumen of the device, an additional fluid lumen, a separate catheter-type device for delivery of the fluid, etc.
- FIG. 7B illustrates an additional variation of a fastening system 150 of the present invention.
- the fastener 100 is depicted as being partially ejected from the system 150 .
- the distal portion 158 may include one or more fluid delivery ports 170 in fluid communication with fluid delivery lumen(s) 164 of the tubular member 152 .
- FIG. 7C is a sectional view taken along the lines of 7 C- 7 C of FIG. 7B .
- the tubular member 152 may include a channel 155 to aid in maintaining an orientation of the fastener and/or assist in advancement of the fastener.
- FIG. 7C also illustrates fluid delivery lumens 164 of the tubular member 152 . It is understood that the system may include a single or multiple fluid delivery lumens(s).
- FIGS. 8A-8F illustrate variations of the fastening 150 of the present invention having features that aid in dispensing fasteners.
- FIGS. 8A-8C illustrate delivery systems having gate members 168 of a valve-type configuration.
- the gate member 168 of these variations may comprise a flexible valve having a slit, gap, or opening therein.
- the gate member will function to impede movement of a portion of a surgical fastener from the system. Accordingly, a portion of the gate member will interfere with a portion of the fastener during its advancement in the system or out of the system.
- the gate 168 is illustrated as being placed in the opening 162 of the distal portion 158 , the gate 168 may also be located within a lumen of the system.
- FIG. 8C illustrates a variation of the fastening system 150 of the present invention depicting a fastener 100 that is partially deployed from the system 150 .
- FIGS. 8D-8E illustrate additional features of a fastening system 150 of the present invention.
- the fastener and other features of the system are omitted for
Abstract
Devices and systems related to surgical fasteners and more specifically to surgical fasteners suitable for use in both open procedures, and minimally or less invasive procedures where the operative site is remote from the surgeon.
Description
- The present invention relates to surgical fasteners and more specifically to surgical fasteners suitable for use in both open procedures, and minimally or less invasive procedures where the operative or surgical site is not directly accessible by the surgeon.
- Surgical fasteners are known to be an alternative to traditional suturing techniques for procedures involving tissue closure, connection, or repair. One undesirable aspect of manual suturing is that the suturing process adds time to the overall surgical process. Moreover, manual suturing often requires that the operative area is readily accessible so that the medical practitioner can manipulate the suture and associated needle through both sides of the tissue, connection or repair site. Presently, surgical fasteners are known to provide a means to close an open surgical incision or wound, hold together pieces of soft tissue, attach devices to tissue, or repair torn tissue in orthopedic/musculoskeletal applications. Such surgical fasteners are often used where there is adequate access to the operative area, or for invasive, open procedures.
- Due to the inherent risks and complexities of invasive surgical procedures, there is an increasing need for the ability to perform surgical procedures in a minimally invasive manner. In most cases, the recuperative time and lowered expense of a minimally invasive procedure makes it a far more desirable option to an alternative comparable invasive/open surgical procedure. The use of surgical fasteners in minimally invasive procedures may be desirable to increase the speed and efficiency of the procedure. Such fasteners may also open the possibility of performing a minimally invasive procedure for what was previously limited to an open surgical procedure.
- In addition, suturing techniques requires considerable skill and dexterity especially when tying knots in the suture or otherwise manipulating the suture. The ability of a medical practitioner to manipulate a suture as well as knot the ends of the suture are further complicated when the site is not directly accessible to the practitioner. In such cases, even if the complexity of suturing does not prevent the procedure from being completed in a minimally invasive manner, the length of the procedure is likely to increase.
- Conventional fasteners do not easily lend themselves for use in minimally invasive surgical procedure. As one example, the complexity of the known fastener-delivery devices requires devices with large profiles and limited flexibility further thereby limiting the potential for such devices to access remote locations. Conventional surgical fasteners, especially, “I-shaped” or “H-shaped” fasteners are unsuitable for remote procedures due to their complex deployment mechanisms and inability to navigate tortuous pathways using access devices commonly used for minimally invasive procedures (e.g., catheters, introducer devices, scope-type devices such as endoscopes, bronchoscopes, colonoscopies, etc.). Examples of such fasteners and devices are discussed in U.S. Pat. No. 4,006,747 to Kronenthal et al., U.S. Pat. No. 4,235,238 to Ogiu et al., U.S. Pat. No. 4,669,473 to Richards et al., U.S. Pat. No. 5,941,439 to Kammerer et al,. U.S. Pat. No. 6,039,753 to Meislin, and U.S. Patent Publications US2003/0097148 to Valimaa et al, U.S. 2003/0187465 to Bailly et al. Each of the foregoing patents and/or patent applications is hereby incorporated in their entirety by reference.
- The present invention includes a surgical fastener for deployment through a device (such as tubular device, a needle, cannula, catheter, etc.), where the fastener comprises a first anchor member, a second anchor member, and a connecting portion separating the first and second anchor members, where at least the first anchor member and the second anchor member each are expandable from a first state to a second state where the second state is of a larger size than the first state, where the larger size may be achieved by an increase in displacement (e.g., volume, profile, configuration, etc.) of a portion of the fastener or the entire fastener. For example, as it assumes the second state, the anchor may change in shape or conform to a profile that is of a larger size than the profile of the first state. Alternatively, or in combination, the increase in volume may be achieved by relaxing a previous state of compression of the fastener portion. In the latter case, the fastener portion may comprise a resilient material that is compressible, and/or the fastener portion may be hollow, or have a cavity, such that the outer perimeter of the anchor portion may be folded into the cavity to assume the first state, or compress the cavity to conform to a smaller state.
- The surgical fastener may also comprise a first means for anchoring the fastener, a second means for anchoring the fastener and a connecting portion separating the first and second means for anchoring. Where the means for anchoring may be any of the anchor portions described herein.
- The invention also includes a surgical fastening system comprising, a tubular member having a proximal and distal end and a lumen extending therebetween, the tubular member being sufficiently flexible to navigate tortuous anatomical passages within a human body, a distal portion located at the distal end of the tubular member, the distal portion having a distal tip being configured to pierce tissue, the distal portion having a lumen extending between the tubular member lumen and an opening in the distal portion, at least one surgical fastener slidably located entirely inside the tubular member lumen, where the surgical fastener comprises a first anchor member, a second anchor member, and a connecting portion separating the first and second anchor members, and an advancing member slidably located within the tubular member lumen such that advancement causes a distal portion of the advancing member to advance the surgical fastener through the tubular member. The system of the present invention may be directed to the desired site using a catheter-guidewire configuration, shaped catheter, a steerable catheter, a scope-type of device (e.g., such as endoscopes, gastroscope, colonoscope, bronchoscope, or any type of scope used to access sites within the body.)
- It should be noted that alternate variations of the present invention include fastening system of the present invention used with conventional fasteners and/or fasteners of as described herein.
- The present invention is useful in many surgical procedures requiring fastening systems, including but not limited to, procedures for fastening or repairing tissue or attachment of implant materials to tissue. The present invention is suitable for, but not limited to, use in the heart, stomach, gastro-intestinal tract, etc. While the faster and fastening system may be used in open procedures, the devices and systems may also be used in minimally invasive procedures where the operative site is remotely accessed using minimally invasive techniques including catheterization and/or endoscopic or similar means.
- The inventive devices are especially suited for advancement via a minimally invasive technique by providing features which improve the ability of the surgeon to deploy the fastener with accuracy and effectuate a proper seal with the fastener. The minimally invasive technique also may allow for visual inspection of the placement of the anchor.
- This application incorporates by reference an application filed Mar. 11, 2004 entitled “SURGICAL FASTENING SYSTEM” having application number ______.
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FIGS. 1A-1B , illustrate a side view of a basic variation of a fastener of the present invention. -
FIGS. 2A-2H illustrate additional examples of various fasteners. -
FIGS. 3A-3B illustrate a variation of a fastener having a single diameter (or similar cross-sectional measurement) prior to deployment. -
FIG. 3C illustrates a variation of a fastener having an insert. -
FIGS. 4A-4C illustrate an example of a fastener system deploying a fastener. -
FIGS. 5A-5B illustrate another variation of a fastener system. -
FIG. 6A illustrates a deployed fastener having elastic properties. -
FIGS. 7A-7C illustrate variations of fastening systems of the present invention. -
FIGS. 8A-8F illustrate additional features of fastening systems of the present invention. - The following illustrations are provided as variations of the present invention. It should be understood that there are many combinations of the present invention and that figures illustrating all variations of the invention would be numerous. Therefore, the invention is intended to include combinations of aspects and features of the illustrated embodiments, or combinations of the specific embodiments themselves.
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FIGS. 1A-1B , illustrate a side view of a basic variation of theinventive fastener 100. As seen inFIG. 1A , thefastener 100 includes afirst anchor member 102 and asecond anchor member 104 and a connectingportion 106 separating the twoanchor members 102 104. The “I-type” fastener shape illustrated inFIGS. 1A-1B is merely for illustrative purposes. Naturally, theanchor portions 102 104 may have a variety of shapes, cross-sections, and configuration as discussed herein. However, theanchor portions 102 104 will generally have a shape that allows for retention of a medium (for example, torn/damaged tissue, two or more discrete pieces of tissues, one or more implants to tissue, a combination thereof, etc.) between theanchor portions 102 104 upon deployment of theanchor 100. Portion(s) of thefastener 100 will be operable between a first and second state where in the second state, a portion or portions of thefastener 100 will be of a larger size and/or profile than the first state. In the variation shown inFIG. 1B , thefastener 100anchors 102 104 are configured so that they expand from the first state, shown inFIG. 1A , to a larger second state. - In use, the
fastener 100 may be delivered to the operative site when the portions of thefastener 100 are in the first state. Upon deployment, selected portions of thefastener 100 assume the larger second state. This configuration allows for delivery of thefastener 100 through an opening in the medium where the opening is smaller than a diameter (or other similar dimension) of thefastener 100 portions after deployment. In some variations of the invention, construction of thefastener 100 allows only a portion (e.g., a single anchor, both anchors, the connecting portion, or a combination thereof) to expand into the second state. In other variations, theentire fastener 100 may be constructed to assume the second state upon deployment. It is contemplated, that the various portions of thefastener 100 may expand differently as required for the particular application (e.g., one or more portions expand at a different rate, a different size, etc.) - Expansion of the
fastener 100 from the first to the second state may be accomplished a variety of ways. For example, thefastener 100 may be constructed of a shape or material that allows compression of the fastener portion, either by application of a compressive force or application of a vacuum, etc. Alternatively, or in combination, thefastener 100 may include a material that swells or expands given the addition of a fluid (e.g., natural body fluids or fluids introduced during the surgical procedure.) - Examples of these materials include biodegradeable and non-biodegradeable polymers, elastomers, shape-memory alloys, other alloys, etc.) For example, carbonate copolymer, polyether ester copolymer, albumin, gelatin, starch, cellulose, dextrans, polysaccharides, fibrinogen, poly (D,L lactide), poly (D,L-lactide-co-glycolide), poly (glycolide), poly (hydroxybutyrate), poly (alkylcarbonate) and poly (orthoesters), EVA copolymers, silicone rubber and poly (methylmethacrylate). Particularly preferred polymeric carriers include poly (ethylene-vinyl acetate), poly (D,L-lactic acid) oligomers and polymers, poly (L-lactic acid) oligomers and polymers, poly (glycolic acid), copolymers of lactic acid and glycolic acid, poly (caprolactone), poly (valerolactone), polyanhydrides, copolymers of poly (caprolactone) or poly (lactic acid) with polyethylene glycol, PET, PETE, and blends thereof.
- In any case, the second state of the fastener comprises a larger profile or configuration as compared to the first state. As stated above, this permits securing of the anchoring
portions 102 104 about the medium and/or securing of the connectingportion 106 within the medium. Another advantage of the invention is that the opening in the medium created during deployment of thefastener 100 may be smaller than would otherwise be possible if the fastener did not expand into the second state upon or after deployment. - It is also contemplated that the fastener may incorporate a variety of additives, coatings, adjuncts, etc. For example, the fastener (or only portions of the fastener) may include a lubricious coating to improve advancement of the fastener in the delivery system. The fastener may include non-proliferative drugs, thrombogenic additives, non-thrombogenic additives, non-inflammatory medicines, additives to induce fibrosis for wound closure, anti-platelet, anti-coagulent, growth factors, gene-transductors, cell matrix, glue, cement, protein, hydrophilic, hydrophobic, lipidphillic, lipidphobic, or combinations where appropriate.
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FIGS. 2A-2H illustrate examples ofvarious fasteners 100 of the present invention. It should be understood that thefasteners 100 of the present invention may have a number of configurations as required for the specific application. These figures are intended to illustrate some possible variations of the invention. As noted herein, where possible, combinations of features of various embodiments and the embodiments themselves are within the scope of the invention.FIG. 2A illustrates afastener 100 similar to that shown inFIGS. 1A-1B . FIG. It is contemplated that for the basic configuration of thefastener 100 illustrated inFIG. 2A (and where appropriate for other variations) theanchor portion 102 104 or the connectingportion 106, individually or collectively, may have cross sections of a variety of shapes, including but not limited to circular, rectangular, square, star- shaped, etc. -
FIG. 2B illustrates a variation of thefastener 100 where theanchor portions 102 104 have a spherical shape. In this variation, theanchor portions 102 104 are illustrated as having acavity 108. Thecavity 108 may assist in reducing the size of theanchor portions 102 104 into the first state. Moreover, as described herein, the cavity 108 (as well as other portions of the fastener 100) may serve as a reservoir for various medications, drugs, etc. Furthermore, variations of fasteners of the present invention may be non-porous if the particular application requires (e.g., where prevention of tissue in-growth is required. Alternatively, variations of the fastener may be porous. Furthermore, the fastener may be selected such that certain portions of the fastener are porous while others are non-porous (e.g., porous anchor members combined with a non-porous connecting member, non-porous anchors with a porous connecting member, etc.) In such variations, porous materials may be selected for construction of the anchor or non-porous materials may be altered to contain pores. -
FIG. 2C illustrates another variation of thefastener 100 in which theanchor portions 102 104 comprise cross-shaped members.FIG. 2D illustrates afastener 100 havinganchor portions 102 104 that are planar-disc-shaped. In such a configuration, the increased surface area of theanchor portions 102 104 may provide better contact between thefastener 100 and the medium to allow for tissue in-growth or for delivery of a therapeutic substance carried by thefastener 100.FIG. 2E illustrates a variation of afastener 100 of the present invention where thefirst anchor portion 102 and thesecond anchor portion 104 comprise different shapes. It should be noted that variations of the invention includefasteners 100 having combinations of anchor portions as illustrated herein or variations thereof. -
FIG. 2F illustrates a variation of afastener 100 of the present invention where thefirst anchor portion 102 and thesecond anchor portion 104 extend in different directions. -
FIG. 2G illustrates a variation of thefastener 100 of the present invention where theanchor portions anchor portions anchor portions fastener 100 the pig-tail anchors may be straightened in the device for delivery. Alternatively, the coils may be compressed in a radial dimension to expand upon deployment from the delivery system. A variation of a pig-tail fastener may include a helical shaped fastener or fastener with helical anchor portions. -
FIG. 2H illustrates another variation of the invention where afastener 100 includesprotrusions 112. Theprotrusions 112 may assist in retaining the anchors and or fastener in the deployment site. Alternatively, or in combination, theprotrusions 112 may comprise bio-active substances as described herein. Although the figure illustrates the protrusions as on the anchor portions only, the invention includesfasteners 100 havingprotrusions 112 on the connectingportion 106 as well. Alternatively, theprotrusions 112 may be located only on the connectingportion 106. - The invention also contemplates that the anchor portions described herein may be configured/suited for attachment of external devices/implants/objects/etc. For example, one possible use of the inventive fastener is placing the fastener in the wall of an organ, then attaching an implant to the organ's wall by attaching the implant to the anchor portions of the fastener.
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FIGS. 3A-3B illustrate another variation of afastener 100 of the present invention. In this variation, as shown inFIG. 3A , in the pre-deployment or first state, theanchor portions 102 104 have substantially the same cross sectional measurement as the connectingportion 106. As illustrated inFIG. 3B , when theanchor portions 102 104 assume the second state, they expand to a greater size than the connectingportion 106. As discussed herein, theanchor portions 102 104 may be constructed from a material similar to that of the connectingportion 106 but having different additives or structure to allow for expansion into the second state. Alternatively, portions of thefastener 100 may be formed from different materials and joined, or molded together to form the composite fastener. -
FIG. 3C illustrates another variation of afastener 100 of the present invention. In this variation, thefastener 100 includes aninsert 110. Theinsert 110 may comprise a bioabsorbable material which dissolves/ is absorbed by the body at a slower rate than the remainder of thefastener 100. Alternatively, theinsert 110 may be a nonbiodegradeable/non-bioabsorable material such that as tissue replaces the absorbable fastener material, the insert remains to provide long term retention of tissue. Moreover, theinsert 110 may comprise a metallic material to provide a radiopaque marker for placement, or for subsequent location of the fastening site. Such a combination may be used with absorbable and non-absorbable fasteners. Although theinsert 110 illustrated inFIG. 3C comprises end portions having a larger dimension than the center portion, the invention is not limited as such. -
FIGS. 4A-4C illustrate a basic example of asystem 150 which deploysfasteners 100 of the present invention. As shown inFIG. 4A , thesystem 150 includes atubular member 152 that is sufficiently flexible so that it may navigate tortuous passages to access the surgical site yet it will have sufficient column strength so that it may penetrate tissue to deploy thefastener 100. As such, variations of thetubular member 152 may be reinforced to minimize kinking of the tubular member as it navigates toward the surgical site. In this variation, thetubular member 152 retains afastener 100 in alumen 154 that extends between a proximal and distal end of thetubular member 152. Thefastener 100 is slidably located inside thetubular member 152 and may be advanced using an advancingmember 156 that is also slidably located within thetubular member lumen 154. - It is contemplated that various methods known in the field may be employed to advance/retract the advancing member. For example, the advancing member may simply push the fastener using a linear or rotary type drive system. Alternatively, the advancing member may be an auger type system that advances the fastener with the assistance of rotatable vanes within the tubular member. A pneumatic, hydraulic, or fluid filled actuation may also be used to advance/retract the advancing member. The advancing
member 156 may be a guidewire or other similar type device that is able to deploy thefastener 100 at the operative site. Although not illustrated, thefastener 100 may be removably attached to the advancingmember 156 to improve accuracy in deployment of thefastener 100. In some variations of the invention, thefastener 100 is configured relative to thelumen 154 so that friction retains thefastener 100 within thelumen 154 until deployment of thefastener 100. In such cases, the wall surface and/or diameter of thelumen 154 may be selected to increase the sliding resistance of thefastener 100. In any case, the system will be configured so that upon deployment of the first anchor thefastener 100 will release from the device rather than pulling out of the tissue. - The
system 150 also includes adistal portion 158 located at the distal end of thesystem 150. Thedistal portion 158 has adistal tip 160 configured to pierce tissue and has anopening 162 through which thefastener 100 exits the device. In some variations of the invention, thedistal tip 160 is configured to prevent “coring” of the tissue to minimize the size of any opening created during deployment of the fastener. Instead, thetip 160 configuration has a sharpened area and a taper proximal to the sharpened area so that thetip 160 makes a small puncture and then dilates the opening in the tissue. -
FIG. 4B illustrates thesystem 150 ofFIG. 4A after thedistal portion 158 advances through two layers oftissue anchor portion 102 exits from thesystem 150. As discussed herein, thefastener 100 may expand upon exiting thesystem 150 via being released from the constraint of thesystem 150. Alternatively, or in combination, fluids (not shown) may cause thefastener 100 to increase in size. Such fluids may be introduced during the procedure or may be naturally occurring at the operative site. Therefore, thefastener 100 may expands to a size greater than the opening in tissue that is created by thefastening system 150. Next, thedistal portion 158 andtubular member 152 are retracted through thetissue 1. Once retracted, thesystem 150 deploys the second anchor portion (not illustrated) thereby retaining thetissues 1 between theanchor portions 102 104. -
FIG. 4C illustrates thesystem 150 ofFIGS. 4A and 4B after thedistal portion 158 is withdrawn through thetissue 1 sufficiently enough so that theopening 162 is on the near side of thetissue 1. Once in the appropriate position, thedevice 150 deploys the remaininganchor portion 104. It should be understood that the system illustrated inFIGS. 4A-4C is depicted to show a basic variation of the invention. It is contemplated that the invention includes variations configured to first deploy an anchor portion on a near side of the tissue (e.g., prior to insertion of the distal tip into the tissue), then advance the distal tip into the tissue to deploy the remaining anchor portion on the far side of the tissue. - Although the fastener of the present invention may be delivered through any tubular device such as a cannula, a catheter, polymeric tubing, etc., the fastener may be part of a fastening system that permits deployment of the fastener in remote parts of the body through a variety of minimally invasive procedures. In such cases, the system may include a steerable catheter, or the system may be guided to the site via a separate catheter, a separate steerable catheter, a endoscope-type device, pre-shaped catheter, etc.
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FIGS. 5A-5B illustrate another variation of asystem 150 of the present invention. In this variation, theopening 162 is located at a distal end of the device rather than in a side-wall of the distal portion. In such a variation, thefastener 100 may be located immediately adjacent theopening 162 to prevent the coring of tissue as thedistal tip 160 advances through tissue.FIG. 5B illustrates a sectional view taken along theline 5B-5B ofFIG. 5A . As illustrated, thesystem 150 may include a lumen that is appropriately shaped to orient the anchor and central portions of thefastener 100. For example, the lumen may be extruded to form a channel for the central portion. Additionally, as shown inFIG. 5B , the system may include a multi- lumen design to allow forfluid delivery ports 164 if required. - As discussed herein, upon deployment of the
fastener 100 from thesystem 150, thefastener 100 portions shall increase in size from the first state to a second state where the larger size may be achieved by an increase in volume and/or profile a portion of the fastener or the entire fastener. The invention contemplates that thefastening delivery system 150 may be used to constrain thefastener 100 into the first state, via a compression mechanism. Alternatively, or in combination, thefastener 100 or portions of the fastener may be configured to increase in size given the application of a fluid. The fluid may comprise naturally occurring bodily fluid or fluid delivered by the fastening system or even fluid delivered via a separate device. - As discussed above, one of the functions of the inventive tissue fastener is to retain two pieces of tissue together, retain an implant to the tissue, or close an opening in tissue. The feature of the
inventive fastener 100 relating to expansion of theanchor portions 102 104 permits placement of thefastener 100 using an opening in the tissue that is smaller would otherwise be required. Moreover, fasteners of the present invention may also be configured such that thecentral portion 106 expands into a second state as well. In such variations, expansion of the center portion may allow for expedited healing of the opening in tissue, or for closure and sealing of the opening in the tissue. In additional variations of the invention, thecentral portion 106 may be configured from a material that allows stretching of thecenter portion 106 during deployment. As shown inFIG. 6A , such afastener 100 having elastic properties allows for an increased compressive force on the medium being retained between the fastener. An additional benefit of such an elastic fastener is that the length of the fastener 100 (e.g., as measured in a direction along the central portion) can accommodate a greater range of tissue and/or material thicknesses. -
FIG. 7A illustrates a variation of afastening system 150 of the present invention. Although thesystem 150 depicts asingle fastener 100 located within the device, it is contemplated that thesystem 150 may comprise a number offasteners 100 to permit serial deployment during use of the system. As illustrated, thesystem 150 includes a flexibletubular member 152 extending between having proximal and distal ends and a lumen extending between the ends. Thesystem 150 includes adistal portion 158 the distal end of thetubular member 152. It is contemplated that thedistal portion 158 may comprise a separate material or insert that is coupled to thetubular member 152. Alternatively, thedistal portion 158 may be formed from the same material as thetubular member 152. Thedistal portion 158 includes adistal tip 160 for penetrating tissue (and/or an implant, etc.). Thedistal portion 158 includes a lumen that is in fluid communication with a lumen of thetubular member 152. Thedistal portion 158 also includes anopening 162 through which thefastener 100 deploys. - In the illustrated variation, the
opening 162 is located in a side wall of thedistal portion 158. However, as discussed herein, the opening may be at thedistal tip 160. It is contemplated that thetubular member 152 will have sufficient column strength to allow for penetration of tissue via advancement of thesystem 150. Accordingly, thetubular member 152 may be constructed of a material that provides sufficient flexibility and column strength. Alternatively, thetubular member 152 may include a reinforcingmember 166, such as a coil, braid, or fiber reinforcement. Furthermore, as discussed above, thesystem 150 includes an advancingmember 156 that permits advancement and/or deployment of thefastener 100. To improve advancement and deployment of the fastener, the tubular member and/or advancing member may be selected from materials that minimize the friction between the two members. Alternatively, or in combination, these items may include a lubricious coating to minimize friction. Although not illustrated, thesystem 150 may include an additional fluid delivery means, such as a fluid source where delivery of the fluid occurs via the lumen of the device, an additional fluid lumen, a separate catheter-type device for delivery of the fluid, etc. -
FIG. 7B illustrates an additional variation of afastening system 150 of the present invention. In this variation, thefastener 100 is depicted as being partially ejected from thesystem 150. As shown, thedistal portion 158 may include one or morefluid delivery ports 170 in fluid communication with fluid delivery lumen(s) 164 of thetubular member 152.FIG. 7C is a sectional view taken along the lines of 7C-7C ofFIG. 7B . As shown, thetubular member 152 may include achannel 155 to aid in maintaining an orientation of the fastener and/or assist in advancement of the fastener.FIG. 7C also illustratesfluid delivery lumens 164 of thetubular member 152. It is understood that the system may include a single or multiple fluid delivery lumens(s). -
FIGS. 8A-8F illustrate variations of thefastening 150 of the present invention having features that aid in dispensing fasteners.FIGS. 8A-8C illustrate delivery systems havinggate members 168 of a valve-type configuration. For example, thegate member 168 of these variations may comprise a flexible valve having a slit, gap, or opening therein. The gate member will function to impede movement of a portion of a surgical fastener from the system. Accordingly, a portion of the gate member will interfere with a portion of the fastener during its advancement in the system or out of the system. Although thegate 168 is illustrated as being placed in theopening 162 of thedistal portion 158, thegate 168 may also be located within a lumen of the system.FIG. 8C illustrates a variation of thefastening system 150 of the present invention depicting afastener 100 that is partially deployed from thesystem 150. -
FIGS. 8D-8E illustrate additional features of afastening system 150 of the present invention. The fastener and other features of the system are omitted for
Claims (35)
1. A surgical fastener for deployment through a device, the fastener comprising:
a first anchor member;
a second anchor member;
a connecting portion separating the first and second anchor members; and
where at least the first anchor member and the second anchor member each are expandable from a first state to a second state where the second state is of a larger size than the first state.
2. The surgical fastener of claim 1 , where the second state is of a larger volume than the first state.
3. The surgical fastener of claim 1 , where the first anchor member and second anchor member assume the first state upon application of a vacuum to the anchor members.
4. The surgical fastener of claim 1 , where the first anchor member and second anchor member are compressible upon application of a compressive force and assume the second state upon removal of the compressive force.
5. The surgical fastener of claim 4 , where the first anchor member and second anchor members are sized relative to the device so that the device provides the compressive force upon insertion of the anchor members into the device.
6. The surgical fastener of claim 1 , where connecting portion is also expandable from the first state to the second state where the second state is of a larger volume than the first state.
7. The surgical fastener of claim 1 , where at least the first and second anchor members comprise a material that expands upon contact with a fluid.
8. The surgical fastener of claim 1 , where at least a portion of the anchors or the connecting member members contain a hollow portion.
9. The surgical fastener of claim 1 , where the connecting portion has a greater elasticity than either the first or second anchor member such that when tissue is placed between the anchor members, the connecting member is placed in a tensile state providing a compressive force against the tissue by the anchor members.
10. The surgical fastener of claim 1 , where the connecting portion has a cross sectional area less than a cross sectional area of either the first or second anchor member.
11. The surgical fastener of claim 1 , where the connecting portion has a lower modulus of elasticity than a modulus of elasticity of either the first or second anchor.
12. The surgical fastener of claim 1 , where the connecting portion is formed from a polymer or co-polymer that is different from the remainder of the fastener.
13. The surgical fastener of claim 1 , where the connecting portion and anchors are formed from a polymer or co-polymer.
14. The surgical fastener of claim 1 , further comprising a bioactive substance.
15. The surgical fastener of claim 14 , where the bioactive substance comprises non-proliferative drugs, thrombogenic additives, non-thrombogenic additives, non-inflammatory medicines, additives to induce fibrosis for wound closure, anti-platelet, anti-coagulent, growth factors, gene-transductors, cell matrix, glue, cement, protein, hydrophilic, hydrophobic, lipidphillic, lipidphobic, or combinations where appropriate.
16. The surgical fastener of claim 1 , where the fastener is bioabsorbable.
17. The surgical fastener of claim 1 , where the fastener comprises a shape selected from a group consisting of an I-type fastener, an H-type fastener, a pig-tail fastener, a helical fastener.
18. The surgical fastener of claim 1 , where the fastener comprises a plurality of pores adapted to facilitate tissue ingrowth.
19. The surgical fastener of claim 1 , where at least the first and second anchor member comprises a material selected from the group consisting of poly (ethylene-vinyl acetate), poly (D,L-lactic acid) oligomers and polymers, poly (L-lactic acid) oligomers and polymers, poly (glycolic acid), copolymers of lactic acid and glycolic acid, poly (caprolactone), poly (valerolactone), polyanhydrides, copolymers of poly (caprolactone) or poly (lactic acid) with polyethylene glycol, PET, PETE, and blends thereof
20. The surgical fastener of claim 1 , where the first anchor member comprises a shape selected from the group consisting of a bar, disc, sphere, cylinder, a helical and a pig-tail shape
21. The surgical fastener of claim 20 , where the second anchor member comprises a shape selected from the group consisting of a bar, disc, sphere, a helical and cylinder.
22. The surgical fastener of claim 1 , further comprising an insert within a fastener material forming the fastener.
23. The surgical fastener of claim 22 , where the insert comprises a material different from the fastener material.
24. The surgical fastener of claim 22 , where the insert comprises a non-biodegradeable material.
25. The surgical fastener of claim 22 , where the insert comprises a metallic material.
26. The surgical fastener of claim 22 , where the insert material degrades slower than the fastener material.
27. The surgical fastener of claim 22 , where the insert material is radiopaque.
28. A surgical fastener for deployment through a device, the fastener comprising:
a first means for anchoring the fastener;
a second means for anchoring the fastener and;
a connecting portion separating the first and second means for anchoring.
29. The surgical fastener of claim 28 , where at least the first and second means for anchoring comprise a material that expands upon contact with a fluid.
30. The surgical fastener of claim 28 , where the connecting portion has a greater elasticity than either the first or second means for anchoring such that when tissue is placed between the means for anchoring, the connecting member is placed in a tensile state providing a compressive force against the tissue by the means for anchoring.
31. The surgical fastener of claim 28 , where the connecting portion is formed from a polymer or co-polymer that is different from the remainder of the fastener.
32. The surgical fastener of claim 28 , further comprising a bioactive substance.
33. The surgical fastener of claim 28 , where the bioactive substance comprises non-proliferative drugs, thrombogenic additives, non-thrombogenic additives, non-inflammatory medicines, additives to induce fibrosis for wound closure, anti-platelet, anti-coagulent, growth factors, gene-transductors, cell matrix, glue, cement, protein, hydrophilic, hydrophobic, lipidphillic, lipidphobic, or combinations where appropriate.
34. The surgical fastener of claim 28 , where at least the first and second means for anchoring comprises a material selected from the group consisting of poly (ethylene-vinyl acetate), poly (D,L-lactic acid) oligomers and polymers, poly (L-lactic acid) oligomers and polymers, poly (glycolic acid), copolymers of lactic acid and glycolic acid, poly (caprolactone), poly (valerolactone), polyanhydrides, copolymers of poly (caprolactone) or poly (lactic acid) with polyethylene glycol, PET, PETE, and blends thereof
35. The surgical fastener of claim 28 , where the first and second means for anchoring comprises a shape selected from the group consisting of a bar, disc, sphere, cylinder, a helical and a pig-tail shape
Priority Applications (4)
Application Number | Priority Date | Filing Date | Title |
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PCT/US2005/007878 WO2005086885A2 (en) | 2004-03-11 | 2005-03-10 | Surgical fastening system |
US11/313,193 US20060100643A1 (en) | 2004-03-11 | 2005-12-19 | Surgical fastening system |
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US11/313,193 Abandoned US20060100643A1 (en) | 2004-03-11 | 2005-12-19 | Surgical fastening system |
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US11/313,193 Abandoned US20060100643A1 (en) | 2004-03-11 | 2005-12-19 | Surgical fastening system |
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Also Published As
Publication number | Publication date |
---|---|
US20060100643A1 (en) | 2006-05-11 |
US7066944B2 (en) | 2006-06-27 |
US20050203552A1 (en) | 2005-09-15 |
WO2005086885A3 (en) | 2005-12-01 |
WO2005086885A2 (en) | 2005-09-22 |
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