US20060142791A1 - Anastomosis device and method - Google Patents

Abstract

An anastomosis device for use in coupling an end of a graft vessel to a side of a target vessel. The target vessel has an opening formed in a side wall thereof for insertion of the device. The device comprises a tubular member, at least a portion thereof being radially compressible to a compressed state for insertion of the tubular member into the opening in the target vessel and expandable from the compressed state to an expanded state for engagement of an inner graft vessel surface with an inner surface of the target vessel after insertion of the tubular member into the opening in the side wall of the target vessel. The compressible portion of the tubular member has an inner surface and an outer surface defining a wall thickness therebetween. The wall thickness of the compressible portion in its compressed state is less than the wall thickness of the compressible portion in its expanded state.

Description

FIELD OF THE INVENTION
• The present invention relates generally to medical devices and methods for performing a vascular anastomosis and, more particularly, to preferred devices and methods for sealingly joining a graft vessel, such as a coronary bypass graft, to the side wall of a target vessel, such as a coronary artery, in an anastomosis.
BACKGROUND OF THE INVENTION
• A manifestation of coronary artery disease is the build-up of plaque on the inner walls of the coronary arteries, which causes narrowing or complete closure of these arteries, resulting in insufficient blood flow. This deprives the heart muscle of oxygen and nutrients, leading to ischemia, possible myocardial infarction, and even death. Surgery to alleviate this problem often involves creating an anastomosis between a coronary artery and a graft vessel to restore a blood flow path to essential tissues. An anastomosis is a surgical procedure by which two vascular structures, such as a graft vessel and a coronary artery, are interconnected.
• Current methods available for creating an anastomosis include hand suturing the vessels together. Connection of interrupted vessels with stitches has inherent drawbacks. For example, it is difficult to perform and requires great skill and experience on the part of the surgeon due in large part to the extremely small scale of the vessels. For example, the coronary arteries typically have a diameter in the range of between about 1 to 5 mm, and the graft vessels have a diameter on the order of about 1 to 4 mm for an arterial graft such as a mammary artery, or about 4 to 8 mm for a vein graft such as a saphenous vein. Other drawbacks of connection with stitches are the long duration of the operation, during which period in conventional open-heart coronary artery bypass graft (CABG) surgery the heart is arrested and the patient is maintained under cardioplegic arrest and cardiopulmonary bypass. Cardiopulmonary bypass has been shown to be the cause of many of the complications that have been reported in conventional CABG, such as stroke. The period of cardiopulmonary bypass should be minimized, if not avoided altogether, to reduce patient morbidity.
• One approach to coronary artery bypass grafting that avoids cardiopulmonary bypass is performing the suturing procedure on a beating heart. At present, however, safe, reproducible, and precise anastomosis between a stenotic coronary artery and a bypass graft vessel presents numerous obstacles including continuous cardiac translational motion which makes meticulous microsurgical placement of graft sutures extremely difficult. The constant translational motion of the heart and bleeding from the opening in the coronary artery hinder precise suture placement in the often tiny coronary vessel.
• The above mentioned drawbacks of hand suturing have led to the development of various approaches to stitchless vascular connection or anastomosis which has the advantage of quick and simple execution and undamaged vascular endothelium. Some approaches to stitchless anastomosis used rigid rings prepared from various materials. For example, Geotz et al., INTERNAL MAMMARY—CORONARY ARTERY ANASTOMOSIS—A Nonsuture Method Employing Tantalum Rings, J. Thoracic and Cardiovasc. Surg. Vol. 41 No. 3, 1961, pp. 378-386, discloses a method for joining blood vessels together using polished siliconized tantalum rings which are circumferentially grooved. The free end of the internal mammary is passed through a ring chosen according to the size of the stenotic coronary artery. The free end of the mammary artery is everted over one end of the ring as a cuff and fixed with a silk ligature which is tied around the most proximal of the circular grooves in the ring. The cuffed internal mammary artery is inserted into an incision in the target coronary artery. The ring is fixed in place and sealingly joined to the target coronary artery by tying one or more sutures circumferentially around the target vessel and into one or more circular grooves in the ring. An intimal-to-intimal anastomosis results and dissection of blood between the coronary artery and the cuffed internal mammary artery is largely prevented.
• The use of metallic coupling rings is also disclosed in Carter et al., Direct Nonsuture Coronary Artery Anastomosis in the Dog, Annals of Surgery, Volume 148, No. 2, 1958, pp. 212-218 (describing use of rigid polyethylene rings for stitchless vascular connections). Moreover, for example, U.S. Pat. No. 4,624,257 to Berggren et al. describes a device consisting of a pair of rigid rings each having a central opening through which the end of the coronary or graft vessel is drawn and everted over the rings. A set of sharp pins extends outwardly from the face of each ring and pierce through the vessel wall in the everted configuration. The rings are then joined together to align the end of the graft vessel with the opening in the target vessel.
• However, no permanently satisfactory results have been reported with the use of rigid rings. A rigid ring presents a foreign body of relatively heavy weight which does not heal well and produces pressure necrosis. Moreover, the use of rigid rings that completely encircle the graft vessel and the arteriotomy creates a severe “compliance mismatch” relative to both the coronary artery and the graft vessel at the anastomosis site which could lead to thrombosis. That is, recent studies suggest that the anastomosis site should not be dramatically different in compliance relative to either the coronary artery or the vascular graft, which is the case when using rigid rings to sealingly join two vessels together.
• Another method currently available for stitchless anastomosis involves the use of stapling devices. These instruments are not easily adaptable for use in vascular anastomosis. It is often difficult to manipulate these devices through the vessels without inadvertently piercing a side wall of the vessel. Moreover, as noted above, the scale of the vessels is extremely small, and it is extremely difficult to construct a stapling device that can work reliably on such a small scale to provide a consistent and precise leak-free vascular anastomosis.
SUMMARY OF THE INVENTION
• The present invention involves improvements to devices and methods for performing vascular anastomoses. The invention facilitates positioning one vessel in the fluid path of another vessel to enhance the fluid flow juncture therebetween. In one aspect of the invention, a graft vessel, such as an internal mammary artery, is sealingly joined to a target vessel, such as a left anterior descending artery. The present invention eliminates the need for meticulous suturing and may reduce the amount of time required to make an anastomosis, while still providing a substantially safe, leak-free anastomosis.
• In one aspect of the present invention, an anastomosis device generally comprises a tubular member. At least a portion of the tubular member is radially compressible to a compressed state for insertion of the tubular member into an opening formed in a target vessel and expandable from the compressed state to an expanded state for engagement of the graft vessel with an inner surface of the target vessel after insertion of the tubular member into the opening in the side wall of the target vessel. The compressible portion of the tubular member has an inner surface and an outer surface defining a wall thickness therebetween. The wall thickness of the compressible portion in its compressed state is less than the wall thickness of the compressible portion in its expanded state.
• A method of the present invention generally comprises the steps of providing a graft vessel with a fastener coupled thereto, the fastener comprising a radially compressible portion; exerting an inwardly directed radial force over at least a portion of the compressible portion until the compressible portion has an outer diameter smaller than the diameter of an opening formed in a side wall of the target vessel; inserting at least a portion of the fastener into the opening in the side wall of the target vessel; and removing the radial force to allow the compressible portion of the fastener to radially expand to sealingly engage the graft vessel with an inner wall of 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 view of an anastomosis device of the present invention showing a graft coupling member coupled to an end of a tubular member.
• FIG. 1A is a cross-sectional view of the anastomosis device ofFIG. 1 taken through the line A-A ofFIG. 1.
• FIG. 2 shows the anastomosis device ofFIG. 1 prior to insertion of the device into an opening in an introducer.
• FIG. 2A shows the anastomosis device ofFIG. 1 prior to insertion of the device into an opening in an alternative embodiment of the introducer ofFIG. 2.
• FIG. 3 is an elevated view of the anastomosis device ofFIG. 2 with a free end of a graft vessel inserted therein.
• FIG. 4 is an elevated view of the anastomosis device ofFIG. 3 with the device inserted into the introducer showing the graft coupling member in a compressed state within the introducer.
• FIG. 5 is an elevated view of the anastomosis device ofFIG. 4 with the free end of the graft vessel shown extending longitudinally from an end of the introducer.
• FIG. 6 is an elevated view of the anastomosis device ofFIG. 5 with the free end of the graft vessel everted over an end of the introducer.
• FIG. 7 is an elevated view of the anastomosis device ofFIG. 6 showing a portion of the graft coupling member extending longitudinally from an end of the introducer and showing the application of one or more sutures between the everted graft vessel and the graft coupling member.
• FIG. 7A is an elevated view of the anastomosis device ofFIG. 1 shown inserted into the introducer ofFIG. 2A.
• FIG. 8 is an elevated view of the anastomosis device ofFIG. 7 inserted into a target vessel through an incision in the target vessel.
• FIG. 9 is an elevated view of the anastomosis device ofFIG. 8 after the introducer has been removed from the fastener showing the completed anastomosis.
• FIG. 10 is an alternative embodiment of the anastomosis device ofFIG. 1.
• FIG. 11 shows the anastomosis device ofFIG. 10 with a graft vessel inserted therein prior to insertion of the device into an opening in the tubular introducer.
• FIG. 12 is an elevated view of the anastomosis device ofFIG. 11 with the device inserted into the introducer and showing the tubular member in a compressed state within the introducer.
• FIG. 13 is an elevated view of the anastomosis device ofFIG. 12 with the free end of the graft vessel everted over an end of the introducer.
• FIG. 14 is an elevated view of the anastomosis device ofFIG. 13 showing a portion of the tubular member extending longitudinally from an end of the introducer and showing the application of one or more sutures between the everted graft vessel and the tubular member.
• FIG. 15 is an elevated view of the anastomosis device ofFIG. 14 inserted into the target vessel through an incision in the target vessel.
• FIG. 16 is an elevated view of the anastomosis device ofFIG. 15 after the introducer has been removed from the fastener showing the completed anastomosis.
DESCRIPTION OF THE INVENTION
• Referring now to the drawings, and first toFIGS. 1 and 1A, an anastomosis device constructed according to the principles of the present invention is shown and generally indicated withreference numeral8. The anastomosis device (or fastener)8 is used to connect agraft vessel10, such as a thoracic artery, to atarget vessel12, such as a coronary artery, i.e., the left anterior descending artery. For example, the device may be used in an end-to-side distal anastomosis to sealingly join a thoracic artery or a saphenous vein graft to a coronary artery. Theanastomosis device8 of the present invention may also be used in connecting various other vessels or arteries and may be used to connect synthetic vascular grafts to an artery.
• Thefastener8 preferably comprises an elongated, flexibletubular member20 and a radially compressible, elongatedgraft coupling member30 which is coupled to an external surface of thetubular member20 at one end of thetubular member20. Thegraft coupling member30 can be coupled to thetubular member20 with biological glue, other adhesive means, thread, or by any other suitable means. Alternatively, thegraft coupling member30 and thetubular member20 can also be provided as separate parts. Thegraft coupling member30 will be configured to be stretched over one end of thetubular member20 and secured proximal to the end of thetubular member20 by the force of its own natural compressibility or by any of the coupling means described above.
• Thetubular member20 comprises twotubular layers22,26, and a thin flexiblecentral tube24 interposed between the two tubular layers. The tubular layers are preferably formed from a biocompatible, implantable plastic material. Thecentral tube24 is preferably formed from a biocompatible coil such as medical grade stainless steel or nitinol wire or ribbon, but may also be formed from any other sufficiently rigid, biocompatible material such as a plastic, polyurethane or polycarbonate material, or any other suitable material as is well known to a person of ordinary skill in the art. The inner and outertubular layers22,26 are preferably formed from a material having a low durometer hardness to provide sufficient flexibility to allow the tubular member to bend at an angle of approximately 30- to 60-along a central longitudinal axis of the member. Preferably, the inner andouter layers22,26 are made from an implantable, flexible plastic such as silicone, although any other suitable flexible, implantable biocompatible material as is well known to persons of ordinary skill in the art may be used. The inner andouter layers22,26 are preferably bonded together (similar to braided shafts) by conventional means and thecentral tube24 is locked between two layers.
• The innerplastic tube22 is generally necessary to prevent thecentral coil24 from scraping and damaging thegraft vessel10. Thecentral coil24 provides strength to thetubular member20 to prevent it from kinking, yet is sufficiently flexible to allow thetubular member20 to be inserted into thetarget vessel12 through anincision16 formed therein. The outer plastictubular layer26 allows thegraft coupling member30 to be more easily fitted over thetubular member20 and coupled thereto. Thetubular member20 is preferably between about 4.0 and 12.0 mm in length, and more preferably about 5.0 to 8.0 mm, for example. As shown inFIG. 1, the inner andouter layers22,26 andcentral coil24 preferably extend the full length of thetubular member20. The diameter of thetubular member20 will vary depending on the size of the graft vessel into which it is inserted. Preferably, the inner diameter of theinner layer22 will generally be between about 0.5 to 6.0 mm for a coronary anastomosis, for example. The total wall thickness oftubular member20 will be between about 0.100 mm and 0.600 mm, and preferably between about 0.100 mm and 0.400 mm, for example. It is to be understood, however, that other types of tubular members made from other types of biocompatible materials and different size tubular members may be used without departing from the scope of the invention. For example, thetubular member20 may be formed from a one-piece flexible tube (not shown).
• The graft coupling member (compressible portion)30 comprises a tube formed from a biocompatible, radially compressible material. By “radially compressible”, it is meant that thegraft coupling member30 is generally uniformly radially transformable between a free, normal expanded state and one or more compressed states in which thegraft coupling member30 has a smaller diameter than in its normal expanded state. In a preferred embodiment, the biocompatible material comprises a non-metallic foam material which is radially self-expandable. By “self-expandable”, it is meant that the foam material forming thegraft tubular member30 is biased to its expanded state (i.e., will naturally tend to radially migrate back towards its free, normal expanded state from its compressed state). Thecoupling member30 has an inner surface and an outer surface defining a wall thickness therebetween. The wall thickness of the coupling member in its compressed state is less than the wall thickness of the member in its expanded state. The foam material may be conventional biocompatible foam such as 100 pores per inch foam material, for example. The foam material is substantially radially compressible to allow thegraft vessel10 to be coupled to the foam and to permit thefastener8 to move longitudinally within thetarget vessel12 as will be described in greater detail below. The diameter of thegraft coupling member30 will vary depending on the size of thetarget vessel12 into which thefastener8 is inserted. Preferably, the inner diameter of thegraft coupling member30 will be about 10 to 30% smaller than the outside diameter of thetubular member20, and the outside diameter ofgraft coupling member30 will preferably be between about 10 to 80% larger than an inside diameter of thetarget vessel12.
• FIGS. 2-9 show an exemplary use of theanastomosis device8 of the present invention in an open surgical coronary artery bypass graft procedure via a median sternotomy. This example is meant to be by illustration only, and in no way is meant to be limiting. The present invention can be used in other cardiac surgery procedures such as minimally invasive direct coronary artery bypass grafting (MIDCAB) on a beating heart through a small incision (thoracotomy) (about 6-8 cm) in the left side of the chest wall, in endoscopic minimally invasive cardiac surgery bypass graft procedures, and in other vascular procedures to join two vessels together. By way of example, the left internal thoracic artery is used as thegraft vessel10. In this example, the left anterior descending artery is used as thetarget vessel12 and contains a build-up of plaque or narrowing13. If left untreated, this diseased artery may lead to insufficient blood flow and eventual angina, ischemia, and possibly myocardial infarction.
• Conventional coronary bypass graft procedures require that a source of arterial blood be prepared for subsequent bypass connection to the diseased artery. An arterial graft can be used to provide a source of blood flow, or a free vessel graft may be used and connected at the proximal end to a source of blood flow. Preferably, the source of blood flow is any one of a number of existing arteries that are dissected in preparation for the bypass graft procedure. In many instances, it is preferred to use either the left or right internal thoracic artery. In multiple bypass procedures, it may be necessary to use free graft vessels such as the saphenous vein, gastroepiploic artery in the abdomen, and other arteries harvested from the patient's body as well as synthetic graft materials, such as Dacron or Gortex grafts. If a free graft vessel is used, the upstream end (proximal) of the dissected vessel, which is the arterial blood source, will be secured to the aorta to provide the desired bypass blood flow, and the downstream end (distal) of the dissected vessel will be connected to the target vessel in a distal anastomosis.
• In order to perform an anastomosis with thefastener8 of the present invention, thegraft vessel10 is first coupled to thefastener8 by inserting a free end of thegraft vessel10 through an opening in thetubular member20 with a conventional insertion device (not shown) and moving thegraft vessel10 longitudinally within thetubular member20 until the free end of the graft vessel extends a short distance beyond an end of the tubular member as shown inFIG. 3. Thefastener8 with thegraft coupling member30 attached thereto is then inserted into an opening in atubular introducer40 which has an inner diameter smaller than an outside diameter of thegraft coupling member30 but larger than an outside diameter of the flexible tubular member20 (FIG. 2). Theintroducer40 preferably includes at least one longitudinal perforation (not shown) to allow for easy removal of the introducer as further described below. The inner wall of theintroducer40 will radially compress thegraft coupling member30 into its at least one compressed state. The free end of thegraft vessel10 is then everted over an end of theintroducer40 as shown inFIG. 6. Theintroducer40 is then pulled back to a short distance over the fastener8 (while holding tubular member20) to a position in which at least an end portion of thegraft coupling member30 is exposed and extends a short distance from an end of theintroducer40 and engages with a portion of thegraft vessel10 in the everted configuration (FIG. 7). The natural adhesiveness ofgraft vessel10 may be sufficient to secure thegraft vessel10 to thegraft coupling member30. If necessary, one ormore sutures50 may be applied to thegraft vessel10 and thegraft coupling member30 to secure thegraft vessel10 to thefastener8 in the event that the natural adhesiveness and compressibility of thegraft vessel10 is insufficient to temporarily secure it to thegraft coupling member30. Alternatively, thegraft vessel10 can be secured to thegraft coupling member30 with biological glue, other adhesive means, by tying one or more sutures circumferentially around thegraft vessel10, or by any other suitable means.
• An alternative embodiment of thetubular introducer40′ is shown inFIGS. 2A and 7A. The introducer includes at least onegroove42 formed in one end of the wall of the introducer. One ormore sutures50 can be inserted through thegroove42 to secure the evertedgraft vessel10 to thegraft coupling member30. It is to be understood that the introducer may have configurations other than those shown herein without departing from the scope of the invention.
• The introducer (40 or40′) is then introduced into thetarget vessel12 through an incision (opening)16 formed in a side wall of the target vessel12 (FIG. 8). Theincision16 can be made with the use of a conventional scalpel or other appropriate cutting instrument. Alternatively, a circular or oval punch may be used to facilitate the arteriotomy. Thefastener8 is preferably positioned in thetarget vessel12 viaintroducer40,40′ such that at least an end portion of thegraft coupling member30 extends generally coaxial with thetarget vessel12. With thefastener8 securely positioned in thetarget vessel12 via theintroducer40,40′, the introducer can be pulled back over the fastener to allow thegraft coupling member30 to radially expand back towards its normal expanded state to sealingly engage the fastener with an inner wall of the target vessel to complete the anastomosis. Theintroducer40,40′ preferably will be a conventional peel-away introducer such as that manufactured by Modified Polymer Components, Inc. of Sunnyvale, Calif., so that it can be easily separated and removed from thefastener8 andgraft vessel10.
• As shown inFIG. 9, the self-expanding nature of thegraft coupling member30 permits thegraft coupling member30 to radially expand to sealingly engage thegraft vessel10 with an inner wall of thetarget vessel12 to complete the anastomosis. The engagement of thefastener8 with thegraft vessel10 and inner wall of thetarget vessel12 prevents substantial longitudinal movement of thefastener8 within the target vessel. If necessary, one or more sutures can be applied to the anastomosis site to prevent thegraft vessel10 from being pulled out from thetarget vessel12. The foam material forming thegraft coupling member30 will apply a gentle circumferentially uniform, radial pressure against theinverted graft vessel10 and the inner wall of thetarget vessel12. An intima-to-intima anastomosis results. The flexibility of the foam material and thetubular member20 permits thefastener device8 to be substantially compliant with thetarget vessel12 and thegraft vessel10 to reduce the onset of thrombosis.
• If required, cardiac stabilization such as described in co-pending provisional patent application Ser. No. 60/055,127, for Compositions, Apparatus and Methods For Facilitating Surgical Procedures, filed Aug. 8, 1997 and invented by Francis G. Duhaylongsod, M.D, may be used during the procedure. Other pharmacological or mechanical methods may also be used.
• In an alternative embodiment of the present invention shown inFIG. 10, wherein like numerals represent like parts, thefastener60 shown therein comprises a single,elongated tubular member70 made from a radially compressible and radially self-expandable material, preferably a non-metallic foam material. The foam material is preferably sufficiently radially rigid to maintain its shape within thetarget vessel12 to provide a fluid-tight seal, and should also be sufficiently flexible to be inserted through anincision16 in thetarget vessel12. The foam material in this embodiment is preferably foam such as manufactured by W. L. Gore of Arizona, for example. Alternatively, the foam may be a material having 100 pores per inch as described above. The outer diameter of thetubular member70 in its free expanded state is preferably between about 10 to 80% larger than the inner diameter of thetarget vessel12 into which it is inserted, and the inner diameter of thetubular member70 in its free expanded state is preferably about 10% to 30% larger than the outer diameter of thegraft vessel10. Thetubular member70 is preferably between about 4.0 and 12.0 mm in length, and more preferably about 5.0 to 8.0 mm in length, for example.
• Thegraft vessel10 may be coupled to thetubular member70 and inserted into thetarget vessel12 in substantially the same way as described above for the tubular member/graft coupling member combination ofFIGS. 1-9. Referring toFIGS. 11-16, thefoam tubular member70 andgraft vessel10 is inserted into an opening in atubular introducer40 which has an inner diameter which is smaller than an outside diameter of thetubular member70, as shown inFIG. 11. The inner wall of theintroducer40 will radially compress thetubular member70 into a compressed state. A free end of thegraft vessel10 is then inserted through an opening in thetubular member70 and everted over an end of the introducer40 (FIGS. 12 and 13). Theintroducer40 can then be pulled back a short distance over the tubular member70 (while holding tubular member70) to a position in which at least an end portion of thetubular member70 is exposed and extends a short distance from an end of theintroducer40 and engages a portion of thegraft vessel10 in the everted configuration (FIG. 14). One ormore sutures50 may be applied between thegraft vessel10 and thetubular member70 to secure thegraft vessel10 to thetubular member70. Alternatively, thegraft vessel10 may be secured to thetubular member70 with biological glue, other adhesive means, by trying one or more sutures circumferentially around thegraft vessel10, or by any other suitable means.
• Alternatively, thetubular member70 may be coupled to thegraft vessel10 by providing an introducer (not shown) as described above with reference toFIG. 7A having at least one groove in a wall of the introducer which extends axially from an end of the introducer. One or more sutures can be provided through the groove to secure the evertedgraft vessel10 to thetubular member70. Theintroducer40 is then introduced into thetarget vessel12 through anincision16 in a wall of thetarget vessel12 and pulled back over the tubular member70 (FIG. 15). Thetubular member70 will then radially expand back towards its free, normally expanded state to sealingly join thegraft vessel10 to thetarget vessel12 in a compliant, patent anastomosis (FIG. 16). If necessary, one or more stay sutures can be applied to the anastomosis site to prevent thegraft vessel10 from pulling out thetarget vessel12. Theintroducer40 can then be peeled away from thetubular member70 and thegraft vessel10 to complete the anastomosis procedure.
• While the above is a complete description of the preferred devices and methods of the invention, various alternatives, substitutions, modifications, and equivalents of the devices and methods described are possible without departing from the principles thereof. For example, it may be possible for a surgeon to radially compress the graft coupling member with his fingers or other appropriate surgical instrument without requiring the use of a separate tubular introducer. The surgeon can then deftly evert the graft vessel over the compressed graft coupling member (or one-piece tubular member) to couple them to one another. The surgeon can then use his fingers to continue to radially compress the graft coupling member as it is inserted into the target vessel through an incision formed therein. By removing his fingers from engagement with the graft coupling member, the graft coupling member will tend to radially expand back towards its normal expanded state to sealingly engage the graft vessel with an inner wall of the target vessel in a completed anastomosis. Similarly, other alternatives, substitutions, modifications and equivalents are possible without departing from the scope of the inventions described herein. Therefore, nothing disclosed above should be taken to limit the scope of the invention, which is defined by the appended claims.
• All references cited herein are incorporated by reference.

Claims (10)

1-30. (canceled)

31. A method for coupling a graft vessel and a target vessel in an end-to-side anastomosis comprising the steps of:

everting a free end of the graft vessel over an end of the coupling member;

coupling the graft vessel to a coupling member, the coupling member comprising a radially compressible portion;

exerting an inwardly directed radial force over at least a portion of the compressible portion until the coupling member has an outer diameter smaller than the diameter of an opening formed in a side wall of the target vessel;

inserting at least a portion of the coupling member into the opening in the side wall of the target vessel with a portion of the graft vessel extending through the opening of the target vessel; and

removing the radial force to allow the compressible portion of the coupling member to radially expand to sealingly engage the graft vessel with the target vessel.

32. The method ofclaim 31, wherein the step of coupling the graft vessel to a coupling member comprises attaching the graft vessel to the coupling member coaxially with the coupling member.

33. The method as set forth inclaim 32, wherein the step of attaching the graft vessel to the coupling member comprises inserting a free end of the graft vessel longitudinally through an opening in the coupling member.

34. The method as set forth inclaim 31, further comprising suturing the everted end of the graft vessel to the coupling member.

35. The method ofclaim 31, wherein the step of exerting a radial force comprises disposing the coupling member within an introducer that has an inner diameter smaller than an outer diameter of the coupling member in its expanded state.

36. The method ofclaim 31, wherein the step of removing the radial force comprises removing the introducer from the coupling member.

37. The method ofclaim 31, wherein the inserting step comprises inserting the coupling member into and through the opening in the side wall of the target vessel.

38. The method ofclaim 31, wherein the inserting step comprises inserting the coupling member into the opening in the side wall of the target vessel such that a portion of the graft vessel extends coaxially within the target vessel.

39. The method ofclaim 31, wherein the step of removing the radial force allows the compressible portion of the coupling member to radially expand to sealingly engage the graft vessel with the inner surface of the target vessel.

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