US20070027461A1 - Tissue connector apparatus and methods - Google Patents

Abstract

A tissue connector assembly having a flexible member and a surgical clip releasably coupled to the flexible member. A needle may be secured to one end portion of the flexible member with the surgical clip coupled to the other end portion of the flexible member. A locking device may be used to couple the flexible member to the surgical clip. A method for connecting tissues is also disclosed. The method includes drawing tissue portions together with a clip assembly and securing the tissue portions together with the clip assembly.

Description

FIELD OF THE INVENTION
• The present invention relates to instruments and methods for connecting body tissues, or body tissue to prostheses.
BACKGROUND OF THE INVENTION
• Minimally invasive surgery has allowed physicians to carry out many surgical procedures with less pain and disability than conventional, open surgery. In performing minimally invasive surgery, the surgeon makes a number of small incisions through the body wall to obtain access to the tissues requiring treatment. Typically, a trocar, which is a pointed, piercing device, is delivered into the body with a cannula. After the trocar pierces the abdominal or thoracic wall, it is removed and the cannula is left with one end in the body cavity, where the operation is to take place, and the other end opening to the outside. A cannula has a small inside diameter, typically 5-10 millimeters, and sometimes up to as much as 20 millimeters. A number of such cannulas are inserted for any given operation.
• A viewing instrument, typically including a miniature video camera or optical telescope, is inserted through one of these cannulas and a variety of surgical instruments and refractors are inserted through others. The image provided by the viewing device may be displayed on a video screen or television monitor, affording the surgeon enhanced visual control over the instruments. Because a commonly used viewing instrument is called an “endoscope,” this type of surgery is often referred to as “endoscopic surgery.” In the abdomen, endoscopic procedures are commonly referred to as laparoscopic surgery, and in the chest, as thoracoscopic surgery. Abdominal procedures may take place either inside the abdominal cavity (in the intraperitoneal space) or in a space created behind the abdominal cavity (in the retroperitoneal space). The retroperitoneal space is particularly useful for operations on the aorta and spine, or abdominal wall hernia.
• Minimally invasive surgery has virtually replaced open surgical techniques for operations such as cholecystectomy and anti-reflux surgery of the esophagus and stomach. This has not occurred in either peripheral vascular surgery or cardiovascular surgery. An important type of vascular surgery is to replace or bypass a diseased, occluded or injured artery. Arterial replacement or bypass grafting has been performed for many years using open surgical techniques and a variety of prosthetic grafts. These grafts are manufactured as fabrics (often from DACRON® (polyester fibers) or TEFLON® (fluorocarbon fibers)) or are prepared as autografts (from the patient's own tissues) or heterografts (from the tissues of animals) or a combination of tissues, semi-synthetic tissues and or alloplastic materials. A graft can be joined to the involved artery in a number of different positions, including end-to-end, end-to-side, and side-to-side. This attachment between artery and graft is known as an anastomosis. Constructing an arterial anastomosis is technically challenging for a surgeon in open surgical procedures, and is almost a technical impossibility using minimally invasive techniques.
• Many factors contribute to the difficulty of performing arterial replacement or bypass grafting. See generally, Wylie, Edwin J. et al., Manual of Vascular Surgery, (Springer-Verlag New York), 1980. One such factor is that the tissues to be joined must be precisely aligned with respect to each other to ensure the integrity and patency of the anastomosis. If one of the tissues is affixed too close to its edge, the suture can rip through the tissue and impair both the tissue and the anastomosis. Another factor is that, even after the tissues are properly aligned, it is difficult and time consuming to pass the needle through the tissues, form the knot in the suture material, and ensure that the suture material does not become tangled. These difficulties are exacerbated by the small size of the artery and graft. The arteries subject to peripheral vascular and cardiovascular surgery typically range in diameter from several millimeters to several centimeters. A graft is typically about the same size as the artery to which it is being attached. Another factor contributing to the difficulty of such procedures is the limited time available to complete the procedure. The time the surgeon has to complete an arterial replacement or bypass graft is limited because there is no blood flowing through the artery while the procedure is being done. If blood flow is not promptly restored, sometimes in as little as thirty minutes, the tissue the artery supplies may experience significant damage, or even death (tissue necrosis). In addition, arterial replacement or bypass grafting is made more difficult by the need to accurately place and space many sutures to achieve a permanent hemostatic seal. Precise placement and spacing of sutures is also required to achieve an anastomosis with long-term patency.
• Highly trained and experienced surgeons are able to perform arterial replacement and bypass grafting in open surgery using conventional sutures and suturing techniques. A suture has a suture needle that is attached or “swedged on” to a long, trailing suture material. The needle must be precisely controlled and accurately placed through both the graft and artery. The trailing suture material must be held with proper tension to keep the graft and artery together, and must be carefully manipulated to prevent the suture material from tangling. In open surgery, these maneuvers can usually be accomplished within the necessary time frame, thus avoiding the subsequent tissue damage (or tissue death) that can result from prolonged occlusion of arterial blood flow.
• A parachuting technique may be used to align the graft with the artery in an end-to-side anastomosis procedure. One or multiple sutures are attached to the graft and artery and are used to pull or “parachute” the graft vessel into alignment with an opening formed in a sidewall of the artery. A drawback to this procedure is the difficulty in preventing the suture from tangling and the time and surgical skill required to tie individual knots when using multiple sutures. Due to space requirements, this procedure is generally limited to open surgery techniques.
• The difficulty of suturing a graft to an artery using minimally invasive surgical techniques has effectively prevented the safe use of this technology in both peripheral vascular and cardiovascular surgical procedures. When a minimally invasive procedure is done in the abdominal cavity, the retroperitoneal space, or chest, the space in which the operation is performed is more limited, and the exposure to the involved organs is more restricted, than with open surgery. Moreover, in a minimally invasive procedure, the instruments used to assist with the operation are passed into the surgical field through cannulas. When manipulating instruments through cannulas, it is extremely difficult to position tissues in their proper alignment with respect to each other, pass a needle through the tissues, form a knot in the suture material once the tissues are aligned, and prevent the suture material from becoming tangled. Therefore, although there have been isolated reports of vascular anastomoses being formed by minimally invasive surgery, no system has been provided for wide-spread surgical use which would allow such procedures to be performed safely within the prescribed time limits.
• As explained above, anastomoses are commonly formed in open surgery by suturing together the tissues to be joined. However, one known system for applying a clip around tissues to be joined in an anastomosis is disclosed in a brochure entitled, “VCS Clip Applier System”, published in 1995 by Auto Suture Company, a Division of U.S. Surgical Corporation. A clip is applied by applying an instrument about the tissue in a nonpenetrating manner, i.e., the clip does not penetrate through the tissues, but rather is clamped down around the tissues. As previously explained, it is imperative in forming an anastomosis that tissues to be joined are properly aligned with respect to each other. The disclosed VCS clip applier has no means for positioning tissues. Before the clip can be applied, the tissues must first be properly positioned with respect to each other, for example by skewering the tissues with a needle as discussed above in common suturing techniques or with forceps to bring the tissues together. It is extremely difficult to perform such positioning techniques in minimally invasive procedures.
• Therefore, there is currently a need for other tissue connecting systems.
SUMMARY OF THE INVENTION
• The present invention involves apparatus and methods for connecting material, at least one of which is tissue. The invention may, for example, be used to secure one vessel to another, such as in a vascular anastomosis.
• According to one aspect of the invention, a tissue connector assembly is provided and comprises a flexible member and a surgical clip which may be releasably coupled to the flexible member. With this construction, a needle may be coupled to the flexible member, which may be in the form of a suture, to facilitate, for example, parachuting suture tissue connecting procedures. The surgical clip may eliminate the need for tying sutures, which requires significant skill, space, and time.
• According to another aspect of the invention a tissue connector assembly comprises a needle, a flexible member coupled to the needle, and a locking device coupled to the flexible member. The locking device is adapted for receiving a surgical fastener. Thus, a surgical fastener may be selected based on a desired procedure and coupled to the locking device to facilitate, for example, parachuting suture tissue connecting procedures as discussed above.
• According to another aspect of the invention, a method for connecting tissues includes drawing portions of tissue together with a clip assembly and securing the tissue portions together with the clip assembly.
• According to another aspect of the invention, multiple portions of material are drawn together with a tissue connector assembly having a clip in an open position. At least one of the portions of material is tissue. The clip is closed to secure the material portions therein. The materials may be drawn together by pulling the tissue connector assembly with at least a portion of the clip positioned in the materials. A needle may be used to insert the tissue connector assembly into the material. A portion of the tissue connector assembly may be manipulated to simultaneously actuate closure of the clip and release the needle from the clip.
• According to another aspect of the invention, a tissue connector assembly is inserted through graft and target vessels with the graft vessel being spaced from the target vessel. The tissue connector assembly has a first end extending from an exterior surface of the graft vessel and a second end extending from an exterior surface of the target vessel. At least one end of the tissue connector assembly is pulled to draw the graft vessel into contact with the target vessel.
• According to another aspect of the invention, a tissue connector assembly is inserted through the graft and target vessels with the graft vessel being spaced from the target vessel and the tissue connector assembly having a first end extending from an exterior surface of the graft vessel and a second end extending from an exterior surface of the target vessel. At least a portion of the tissue connector assembly is pulled to draw the graft vessel into contact with the target vessel.
• The above is a brief description of some deficiencies in the prior art and advantages of the present invention. Other features, advantages, and embodiments of the invention will be apparent to those skilled in the art from the following description, accompanying drawings, and claims.
BRIEF DESCRIPTION OF THE DRAWINGS
• FIG. 1 is a perspective of a tissue connector assembly of the present invention;
• FIG. 2A shows two tissue connector assemblies ofFIG. 1 in a first step for connecting a graft vessel to a target vessel;
• FIG. 2B shows a second step for connecting the graft vessel to the target vessel;
• FIG. 2C shows a third step for connecting the graft vessel to the target vessel;
• FIG. 2D shows the graft vessel connected to the target vessel;
• FIG. 2E is a front view of the connected graft and target vessels ofFIG. 2D, with portions broken away to show detail;
• FIG. 2F is an enlarged view of the tissue connection shown inFIG. 2E;
• FIG. 2G shows an alternate method for connecting the graft vessel to the target vessel with the tissue connector assembly ofFIG. 1;
• FIG. 3A is an enlarged view of a fastener of the tissue connector assembly ofFIG. 1 shown in a closed position;
• FIG. 3B is a side view of the fastener ofFIG. 3A;
• FIG. 3C is an enlarged view of the fastener in an open position;
• FIG. 3D is an enlarged view of an alternate configuration of the fastener shown in a closed position;
• FIG. 3E is an enlarged view of an alternate configuration of the fastener shown in a closed position;
• FIG. 3F is a side view of the fastener ofFIG. 3E;
• FIG. 3G is an enlarged view of an alternate configuration of the fastener shown in a closed position;
• FIG. 4A is a cross-sectional view of a restraining device of the tissue connector assembly ofFIG. 1 in a locked position;
• FIG. 4B is a cross-sectional view of the restraining device ofFIG. 4A taken in theplane including line4B-4B;
• FIG. 4C is a cross-sectional view of the restraining device ofFIG. 4A in an unlocked position;
• FIG. 5 is an alternate embodiment of the restraining device ofFIG. 4A; and
• FIG. 6 is a front view of a second embodiment of a tissue connector assembly of the present invention shown in an open position.
• Corresponding reference characters indicate corresponding parts throughout the several views of the drawings.
DESCRIPTION OF THE INVENTION
• Referring now to the drawings, and first toFIG. 1, a tissue connector assembly constructed according to the principles of the present invention is shown and generally indicated withreference numeral10. Thetissue connector assembly10 may be used to manipulate and align tissues, or tissue and prosthesis with respect to each other and thereafter connect the tissues or tissue and prosthesis together (FIGS. 2A-2G). As used herein, the term graft includes any of the following: homografts, xenografts, allografts, alloplastic materials, and combinations of the foregoing. Thetissue connector assembly10 may be used in vascular surgery to replace or bypass a diseased, occluded, or injured artery by connecting agraft vessel12 to acoronary artery14 or vein in an anastomosis, for example. Thetissue connector assembly10 may be used in open surgical procedures or in minimally invasive or endoscopic procedures for attaching tissue located in the chest, abdominal cavity, or retroperitoneal space. These examples, however, are provided for illustration and are not meant to be limiting.
• In the embodiment shown inFIG. 1, thetissue connector assembly10 generally comprises a penetratingmember16,flexible member18, and fastener or surgical clip20 (FIG. 1). A restraining device, generally indicated at24 and comprising a spring (or coil)26 and a locking device (coupling member) generally indicated at28, is connected to thefastener20 for holding the fastener in a deformed configuration as further described below. Although a particular fastener and accompanying restraining device is shown inFIG. 1, it should be understood that any suitable fastener can be used, including but not limited to the alternate fastener configurations described below. For example, the fastener or surgical clip may be a plastically deformable clip or may comprise two or more parts, at least one of which is movable relative to the other part, such as with a hinged clip.
• The penetrating member orneedle16 has a sharppointed tip30 at its distal end for penetrating tissue. Theneedle16 may be bent as shown inFIG. 1, for example. The diameter of at least a portion of theneedle16 is preferably greater than the diameter of theflexible member18 so that the flexible member can easily be pulled through an opening formed in the tissue by the needle. The distal end of theneedle16 is preferably rigid to facilitate penetration of tissue. The remaining length of theneedle16 may be rigid or flexible to facilitate movement of the needle through the tissue as further described below. Thetip30 of theneedle16 may be conical, tapered, or grounded to attain a three or four facet tip, for example. Theneedle16 may be made from stainless steel or any other suitable material, such as a polymeric material. It is to be understood that theneedle16 may have a shape or radius of curvature other than the one shown, without departing from the scope of the invention. Theneedle16 may also be integrally formed with the flexible member18 (e.g., both needle and flexible member formed of the same material.)
• Theflexible member18 may be in the form of a suture formed from conventional filament material, metal alloy such as nitinol, polymeric material, or any other suitable material. The material may be non-stretchable or stretchable, solid or hollow, and have various cross-sectional diameters. The suture may have a cross-sectional diameter of 0.003 inch, for example. The diameter and length of the suture will vary depending on the specific application. The suture may be attached to theneedle16 by crimping or swaging the needle onto the suture, gluing the suture to the needle, or any other suitable attachment method. Theflexible member18 may have cross-sectional shapes other than the one shown herein.
• One embodiment of a fastener comprises adeformable wire34 made of a shape memory alloy. A nickel titanium (nitinol) based alloy may be used, for example. The nitinol may include additional elements which affect the yield strength of the material or the temperature at which particular pseudoelastic or shape transformation characteristics occur. The transformation temperature may be defined as the temperature at which a shape memory alloy finishes transforming from martensite to austenite upon heating (i.e., A_ftemperature). The shape memory alloy preferably exhibits pseudoelastic (superelastic) behavior when deformed at a temperature slightly above its transformation temperature. At least a portion of the shape memory alloy is converted from its austenitic phase to its martensitic phase when thewire34 is in its deformed configuration. As the stress is removed, the material undergoes a martensitic to austenitic conversion and springs back to its original undeformed configuration. When thewire34 is positioned within the tissue in its undeformed configuration, a residual stress is present to maintain the tissue tightly together (FIG. 2E). In order for thepseudoelastic wire34 to retain sufficient compression force in its undeformed configuration, the wire should not be stressed past its yield point in its deformed configuration to allow complete recovery of the wire to its undeformed configuration. The shape memory alloy is preferably selected with a transformation temperature suitable for use with a stopped heart condition where cold cardioplegia has been injected for temporary paralysis of the heart tissue (e.g., temperatures as low as 8-10 degrees Celsius).
• It is to be understood that the shape memory alloy may also be heat activated, or a combination of heat activation and pseudoelastic properties may be used, as is well known by those skilled in the art.
• The cross-sectional diameter of thewire34 and length of the wire will vary depending on the specific application. The diameter d of thewire34 may be, for example, between 0.001 and 0.015 inch. For coronary bypass applications, the diameter is preferably between 0.001 and 0.008 inch with a diameter D of the loop being between 0.0125 and 0.0875 inch (FIG. 3A). As shown inFIG. 3A, thewire34 has a circular cross-sectional shape. The diameter D of the loop of thefastener20 in its closed position is preferably sized to prevent movement between adjacent tissues. It is to be understood, however, that the wire may have other cross-sectional shapes such as rectangular, or may be formed from multiple strands without departing from the scope of the invention.
• The proximal end of thewire34 may include astop36 having a cross-sectional area greater than the cross-sectional area of the wire andcoil26 to prevent the wire and coil from passing through the tissue. Thestop36 may be attached to the end of thewire34 by welding, gluing or other suitable attachment means or may be formed integrally with the wire by deforming the end of the wire. Thestop36 may also be eliminated to facilitate pulling the fastener completely through the tissue, if, for example, the entire fastener needs to be removed from the vessel during the insertion procedure. The distal end of thewire34 includes anenlarged portion38 for engagement with the restrainingdevice24 as further described below (FIG. 4A). Theenlarged portion38 may be formed by deforming the end of thewire34 by swaging or arc welding, or attaching by welding, swaging, or other suitable means an enlarged portion to the end of the wire.
• Thewire34 has an undeformed or closed configuration (position, state) (FIG. 3A) for keeping or connecting tissue together, and a deformed or open configuration (position, state) (FIG. 3C) for insertion of the wire into tissue. As discussed above, thewire34 is in its closed configuration when in a relaxed state. Thewire34 is preferably not deformed past its yield point in its open position. Accordingly, it may have a U-shaped configuration in its open position to facilitate insertion of the wire through the tissue. It is to be understood that U-shaped configuration may be alternatively substituted by an equivalent structure such as C-shaped, V-shaped, J-shaped, and other similarly shaped configurations. Thewire34 is moved from its closed position to its open position by a restraining device, as further described below. When in its closed position, thewire34 forms a loop with the ends of the wire in a generally side-by-side or overlapping orientation (FIG. 3B).
• Thewire34 may be formed in the above described shape by first wrapping the wire onto a mandrel and heat treating the wire at approximately 400-500 degrees Celsius for approximately 5 to 30 minutes. Thewire34 is then air quenched at room temperature. The mandrel may have a constant diameter or may be conical in shape.
• An alternate configuration of thesurgical clip20 in its closed position is shown inFIG. 3D, and generally indicated at40. Thefastener40 forms a spiral configuration in its closed position for trapping the tissue within a loop formed by the spiral. In its open position, thefastener40 is configured to form less than a full 360 degree turn.
• Another alternate configuration of thesurgical clip20 is shown inFIGS. 3E and 3F in its closed position, and is generally indicated at41. Thefastener41 is formed in a spiral about a central longitudinal axis A. As shown inFIG. 3F, thefastener41 has a generally conical shape along the longitudinal axis A, with a decreasing diameter as the radius of curvature of thefastener41 decreases. Thefastener41 has aninner end portion45 and anouter end portion47, with theenlarged portion38 of the wire being disposed at the outer end portion for engagement with the restrainingdevice24.
• A modification of thefastener41 is shown inFIG. 3G, and generally indicated at43. Thefastener43 is similar to thefastener41 described above, except that theenlarged portion38, which is adapted for engaging a restraining device or releasable locking mechanism, is positioned at theinner end portion45 of the fastener. Placement of the restrainingdevice24 at theinner end portion45 of thefastener43 increases the compression force of the wire in its undeformed position on the tissue and decreases the surface area of the fastener exposed to blood flow.
• It is to be understood that thefastener20,40,41,43 may have undeformed or deformed configurations different than those shown herein without departing from the scope of the invention. In addition, a locking clip (not shown) may also be attached to connect the ends of thefastener20,40,41,43 when the fastener is in its closed position to prevent possible opening of the fastener over time. The locking clip may also be integrally formed with one end of the fastener.
• As shown inFIG. 3C, thewire34 is surrounded by the spring orcoil26 which, along with the lockingdevice28, restrains the wire in its deformed configuration. Thecoil26 comprises a helical wire forming a plurality of loops which define alongitudinal opening44 for receiving the shapememory alloy wire34. Thecoil26 may be formed from a platinum alloy wire having a cross-sectional diameter of approximately 0.0005-0.005 inch, for example. The helical wire may have other cross-sectional shapes and be formed of different materials. Thecoil26 is preferably sized so that when in its free (uncompressed state) it extends the length of thewire34 with one end adjacent thestop36 at the proximal end of the wire and the other end adjacent theenlarged portion38 at the distal end of the wire. It is to be understood that the coil may not extend the full length of the wire. For example, a flange or similar device may be provided on an intermediate portion of thewire34 to limit movement of the coil along the length of the wire.
• When thecoil26 is in its free state (with the wire in its undeformed configuration), loops of the coil are generally spaced from one another and do not exert any significant force on the wire34 (FIG. 3A). When thecoil26 is compressed (with thewire34 in its deformed configuration), loops of the coil on theinner portion46 of the coil are squeezed together with a tight pitch so that the loops are contiguous with one another while loops on theouter portion48 of the coil are spaced from one another (FIG. 3C). This is due to the compressed inner arc length of thecoil26 and the expanded outer arc length of the coil. The compression of the loops on theinner portion46 of thecoil26 exerts a force on the inner side of thewire34 which forces the wire to spread open (i.e., tends to straighten the wire from its closed configuration to its open configuration). The end of thecoil26 adjacent thestop36 is held in a fixed position relative to thewire34. The opposite end of thecoil26 is free to move along thewire34 and is held in place when the coil is in its compressed position by the lockingdevice28.
• The lockingdevice28 of the embodiment shown inFIGS. 1 and 4A-4C comprises aflexible tubular member50 having adistal end portion52 coupled to theflexible member18 and aproximal end portion54 releasably attached to the wire. The lockingdevice28 couples theflexible member18 andneedle16 to theclip20. In addition to releasably coupling theflexible member18 andneedle16 to theclip20, the locking device compresses thecoil26 to bias theclip20 in its open configuration. Thedistal end52 of thetubular member50 is attached to theflexible member18 with a tapered portion ortransition sleeve56 extending from the tubular member to the suture to facilitate insertion of thelocking device28 through tissue. The taperedportion56 is preferably sufficiently curved to facilitate movement of thetissue connector assembly10 through connecting tissue in an anastomosis, for example. The taperedportion56 may be formed from a metal alloy such as stainless steel or a suitable polymeric material and may be solid or in the form of a sleeve. Generally,portion56 gradually diminishes in diameter to provide a smooth, non-stepped transition between the relatively small diameter offlexible member18 to the larger diameter of lockingdevice28. Theflexible member18 may be swaged into the taperedportion56, or a heat shrink plastic covering may hold the flexible member in place. The lockingdevice28 may also be curved.
• Thetubular member50 is movable between a locked position (FIG. 4A) for holding thecoil26 in its compressed position and thewire34 in its deformed position, and an unlocked position (FIG. 4C) for inserting or releasing the wire and coil. Threeslots58 are formed in thetubular member50 extending from theproximal end54 of the member and along at least a portion of the member (FIGS. 4B and 4C). Theslots58 are provided to allow theproximal end54 of thetubular member50 to open for insertion and removal of thewire34 when the tubular member is in its unlocked position (FIG. 4C). It is to be understood that the number ofslots58 and configuration of the slots may vary, or thetubular member50 may be formed to allow expansion of theproximal end54 without the use of slots.
• Theproximal end54 of thetubular member50 includes abore62 having a diameter slightly greater than the outer diameter d of thewire34, but smaller than the diameter of theenlarged portion58 at the distal end of the wire and the outer diameter of thecoil26. Thebore62 extends into acavity64 sized for receiving theenlarged portion38 of thewire34.Member50 may be described as having anannular flange61 for releasably securing theenlarged portion38. As shown inFIG. 4C, upon application of an inwardly directed radial squeezing force on thetubular member50 theproximal end54 of the tubular member is opened to allow for insertion or removal of thewire34. When the force is released (FIG. 4A), thetubular member50 moves back to its locked position and securely holds thewire34 in place and compresses thecoil26. Adisc51 may be inserted into thetubular member50 to act as a fulcrum and cause theproximal end54 of the tubular member to open. Alternatively, thedisc51 may be integrally formed with thetubular member50. As shown inFIG. 4A, the length l of thebore62 orflange61 determines the amount of compression of the coil, which in turn determines the amount of deformation of thewire34. The greater the length l of thebore62, the greater the compression of thecoil26 and the more straightening thewire34 will undergo. The compression of thecoil26 is preferably limited so that thewire34 is not stressed beyond its yield point. This allows thewire34 to revert back to its original undeformed configuration and apply sufficient pressure to hold the connected tissue together.
• It is to be understood that locking devices other than those described above may be used without departing from the scope of the invention. For example, a locking device (not shown) may comprise a tubular member having an opening formed in a sidewall thereof for receiving an end portion of the wire. The end of the wire may be bent so that it is biased to fit within the opening in the sidewall of the tubular member. An instrument, such as a needle holder may then be used to push the wire away from the opening in the tubular member and release the wire from the tubular member. Various other types of locking devices including a spring detent or bayonet type of device may also be used.
• An alternate embodiment of the restraining device is shown inFIG. 5, and generally indicated withreference numeral70. The restrainingdevice70 is used with a tubular (hollow) shapememory alloy wire72 and comprises an elongated member (or mandrel)74 sized for insertion into the wire or tube. Themandrel74 is preferably formed from a material which is stiffer than the material of thewire72 so that upon insertion of the mandrel into the wire, the wire is deformed into its open position. The restrainingdevice70 includes astop76 located at the proximal end of thewire72. The stop operates to prevent the fastener from being pulled through the tissue, and limits axial movement of themandrel74 in the proximal direction (to the right as viewed inFIG. 5). The distal end of themandrel74 is attached to thesuture18 and includes a taperedportion78. The taperedportion78 may be a sleeve or may be solid and may be formed from any suitable metal or polymeric material, for example. It is to be understood that other types of restraining devices may be used without departing from the scope of the invention.
• Another tissue connector assembly is shown inFIG. 6 and generally indicated withreference numeral100. Thetissue connector assembly100 is the same as thefirst embodiment10 except that aneedle102 is attached directly to alocking device104 with thesuture18 of the first embodiment being eliminated. Thetissue connector assembly100 includes theneedle102, a restrainingdevice108, and afastener110.FIG. 6 shows thetissue connector assembly100 with the fastener in its open (deformed) configuration. Thefastener110 may be the same as thefasteners20,40,41,43 described above and shown inFIGS. 3A-3G for the tissue connector assembly of the first embodiment, for example.
• The restrainingdevice108 comprises acoil112 and thelocking device104. Thelocking device104 is similar to thelocking device28 shown inFIGS. 4A-4C, except that the distal end is configured for attachment directly to theneedle102. Theneedle102 may be integrally formed with thelocking device104 or may be swaged, welded, threadably attached, or attached by any other suitable means to the locking device. The restrainingdevice70 shown inFIG. 5 may also be used with thisembodiment100 of the tissue connector assembly.
• As noted above, thetissue connector assemblies10,100 have many uses. They may be especially useful for minimally invasive surgical procedures including creating an anastomosis between avascular graft12 and an artery14 (FIGS. 2A-2G). The anastomosis may be used to replace or bypass a diseased, occluded or injured artery. A coronary bypass graft procedure requires that a source of arterial blood flow be prepared for subsequent bypass connection to a diseased artery. An arterial graft may be used to provide a source of blood flow, or a free graft may be used and connected at the proximal end to a source of blood flow. Preferably, the source of blood flow is one of any number of existing arteries which may be dissected in preparation for the bypass graft procedure. In many instances it is preferred to use the left internal mammary artery (LIMA) or the right internal mammary artery (RIMA), for example. Other vessels which may be used include the saphenous vein, gastroepiploic artery in the abdomen, radial artery, and other arteries harvested from the patient's body as well as synthetic graft materials, such as DACRON® (polyester fibers) or GORETEX® (expanded polytetrafluoroethylene). If a free graft vessel is used, the upstream end of the dissected vessel, which is the arterial blood source, will be secured to the aorta to provide the desired bypass blood flow, as is well known by those skilled in the art. The downstream end of the graft vessel is trimmed for attachment to an artery, such as the left anterior descending coronary (LAD). It is to be understood that the anastomosis may be formed in other vessels or tissue.
• FIGS. 2A-2F show an exemplary use of thetissue connector assemblies10,100 for connecting agraft vessel12 to an artery14 (target vessel). In this example, twotissue connector assemblies10 are used to make connections at generally opposite sides of the graft vessel andtissue connector assemblies100 are used to make connections between those made with assemblies10 (FIG. 6). The procedure may be accomplished with a beating heart procedure with the use of a heart stabilizer to keep the heart stable, for example. The procedure may also be performed endoscopically.
• The patient is first prepped for standard cardiac surgery. After exposure and control of theartery14, occlusion and reperfusion may be performed as required. After the arteriotomy of the snaredgraft vessel12 has been made to the appropriate length, atissue connector assembly10 is attached to the free end of the graft vessel along an edge margin of the vessel. In order to attach theconnector assembly10, the surgeon grasps theneedle16 with a needle holder (e.g., surgical pliers, forceps, or any other suitable instrument) and inserts theneedle16 into the tissue of thegraft vessel12 in a direction from the exterior of the vessel to the interior of the vessel. The surgeon then releases theneedle16 and grasps a forward end of the needle which is now located inside thegraft vessel12 and pulls the needle and a portion of thesuture18 through the vessel. Theneedle16 is passed through anopening120 formed in the sidewall of theartery14 and inserted into the tissue of the artery in a direction from the interior of the artery to the exterior of the artery. The surgeon then grasps theneedle16 located outside theartery14 and pulls the needle and a portion of thesuture18 through the arterial wall. A secondtissue connector assembly10 may be inserted at a location generally 180 degrees from the location of the first tissue connector in a conventional “heel and toe” arrangement.
• Once thetissue connector assemblies10 are inserted, thegraft vessel12 is positioned above and aligned with theopening120 in the sidewall of the artery14 (FIG. 2A). A section of eachsuture18 is located between thegraft vessel12 andartery14. Thefasteners20 and needles16 are pulled generally away from theartery14 to reduce the length of the suture18 (eliminate slack of the suture) between thevessel12 and artery and “parachute” the vessel onto the artery (FIG. 2B). Theneedles16 are then pulled away from theartery14 until eachfastener20 is positioned within thegraft vessel12 and artery with one end of eachfastener20 extending from the vessel and the opposite end of each fastener extending from the artery (FIG. 2C). The edges of thegraft vessel12 andartery14 are positioned adjacent one another to form a continuous interior and exterior surface along the mating portions of the vessel and artery. As shown inFIG. 2F, the tissue is compressed within thefastener20.
• A surgical instrument (e.g., needle holder) is used to radially squeeze each lockingdevice28 to release the locking device from thefastener20. Upon removal of thelocking device28, thecoil26 moves to its free uncompressed state which allows thewire34 to return to its original undeformed closed position (FIG. 2D). As thewires34 move to their closed position the adjacent tissues of thegraft vessel12 andartery14 which were previously pulled together during the parachuting of the graft vessel onto the artery, are squeezed together to securely engage the graft vessel and artery (FIGS. 2E and 2F). It should be noted that as the lockingdevice28 is squeezed two steps are accomplished. Thefastener20 is released from the lockingdevice28, thus allowing thecoil26 to uncompress and thewire34 to move to its closed configuration, and theneedle16 is released from the fastener. Thus, in this embodiment, the lockingdevice28 provides for simultaneous actuating closure of thefastener20 and release of theneedle16 from the fastener.
• Thetissue connector assemblies100 are subsequently inserted at circumferentially spaced locations around the periphery of the graft vessel to sealingly fasten thegraft vessel12 to theartery14. Theneedle102 of thefastener100 is inserted into thegraft vessel12 from the exterior surface of the graft vessel and pushed through the graft vessel andartery14 tissue. The needle holder is then used to pull theneedle102 through the arterial wall. An instrument (same needle holder or other suitable instrument) is used to apply a squeezing force to thelocking device104 to release the wire andcoil112 from theneedle102. This allows thecoil112 to move to its uncompressed configuration and the wire to move to its closed position. It should be noted that thetissue connector assemblies10 may remain in their open position while thetissue connector assemblies100 are inserted into the tissue and moved to their closed position. Thelocking devices28 of thetissue connector assemblies10 may subsequently be removed from thefasteners20 to allow the fasteners to move to their closed position. The number and combination oftissue connectors assemblies10,100 required to sealingly secure the connecting tissues together may vary. For example, onlytissue connector assemblies10 may be used to complete the entire anastomosis.
• Although thecoil26 is shown remaining on the wire (FIG. 2D), it is to be understood that thecoil26 may also be removed from thewire34, leaving only the wire in the connected tissue.
• As an alternative to insertingtissue connector assemblies10 at “heel and toe” locations described above, a number oftissue connectors10 may be inserted generally around the location of the heel. The graft vessel may then be pulled towards the artery to determine whether the opening formed in the sidewall of the artery is large enough before completing the anastomosis.
• Thegraft vessel12 may also be parachuted onto theartery14 in the method shown inFIG. 2G. The needle is inserted into thegraft vessel12 andartery14 as described above and thesuture18 is pulled through the vessel so that thefastener20 is positioned within the vessel and artery. Theneedles16 are then pulled away from theartery14 to “parachute” thegraft vessel12 onto the artery. The anastomosis may then be completed as described above.
• Although the suturing procedure has been described for an end-to-side anastomosis, it should be appreciated that the procedure is applicable to an end-to-end and side-to-side anastomosis, connecting various tissue structures including single and multiple tissue structures, and puncture sites, and connecting tissue to a prosthetic graft or valve, for example.
• It will be observed from the foregoing that the tissue connector assemblies of the present invention have numerous advantages. Importantly, the assemblies are easier and faster to apply than conventional sutures which require tying multiple knots. The assemblies also may be used in minimally invasive procedures including endoscopic procedures.
• All references cited above are incorporated herein by reference.
• The above is a detailed description of a particular embodiment of the invention. It is recognized that departures from the disclosed embodiment may be made within the scope of the invention and that obvious modifications will occur to a person skilled in the art. The full scope of the invention is set out in the claims that follow and their equivalents. Accordingly, the claims and specification should not be construed to unduly narrow the full scope of protection to which the invention is entitled.

Claims (9)

1-38. (canceled)

39. A method for connecting a graft vessel to a target vessel in an anastomosis comprising:

inserting a tissue connector assembly through said graft and target vessels with said graft vessel being spaced from said target vessel and said tissue connector assembly having a first end extending from an exterior surface of said graft vessel and a second end extending from an exterior surface of said target vessel; and

pulling at least a portion of said tissue connector assembly to draw said graft vessel into contact with said target vessel.

40. The method ofclaim 39 further comprising inserting a second tissue connector assembly through said graft and target vessels prior to pulling at least a portion of said tissue connector assembly.

41. The method ofclaim 39 further comprising inserting a plurality of clips into said graft and target vessels after pulling at least a portion of said tissue connector assembly, to sealingly engage said vessels.

42. The method ofclaim 41 further comprising placing said clips into an open configuration prior to inserting said clips into said vessels.

43. The method ofclaim 42 wherein said deforming of said clips includes attaching a restraining device to each of said clips.

44. The method ofclaim 39 wherein said inserting a tissue connector assembly includes inserting said tissue connector assembly through an end margin of said graft vessel and a side of said target vessel.

45. The method ofclaim 39 wherein said inserting a tissue connector assembly includes inserting said tissue connector assembly through an end margin of said graft vessel and an end margin of said target vessel.

46. The method ofclaim 39 wherein said inserting a tissue connector assembly includes inserting said tissue connector assembly through said a side of said graft vessel and a side of said target vessel.

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