US20160113797A1 - Stent delivery system and method of manufacturing same - Google Patents

Abstract

Stent delivery system and method of manufacturing same. The stent delivery system comprises an inner catheter with an enlarged tip disposed at the distal end thereof. A stent engaging sleeve coaxially surrounds and is secured to a portion of the inner catheter proximally contiguous to the tip. The stent engaging sleeve is used to frictionally engage a stent mounted thereover in such a way as to prevent the stent, during deployment, from sliding proximally relative to the inner catheter. The system additionally comprises a self-expandable stent of the type comprising a knitted mesh of nitinol wire flexible in both the radial and longitudinal axes. The stent is mounted over the stent engaging sleeve in a longitudinally stretched state. The system also includes an outer catheter surrounding the stent and stent engaging sleeve, the outer catheter being adapted for axial movement relative to the inner catheter.

Description

CROSS-REFERENCE TO RELATED APPLICATIONS
• This application is a continuation of U.S. application Ser. No. 11/589,493, filed Oct. 30, 2006, which is a continuation of U.S. patent application Ser. No. 10/790,607, filed Mar. 1, 2004, now U.S. Pat. No. 7,127,789, which in turn is a continuation of U.S. patent application Ser. No. 09/767,212, filed Jan. 22, 2001, now U.S. Pat. No. 6,699,274, all of which are incorporated herein by reference.
BACKGROUND
• The present invention relates generally to medical stents (hereinafter “stents”) and relates more particularly to stent delivery systems.
• A stent is a tubular endoprosthesis placed within a body lumen to maintain its patency. For example, a stent may be used to maintain the patency of an esophagus or other passageway occluded by a tumor or of a blood vessel constricted by plaque. Most stents fall into one of the following two classes: (i) balloon-expandable stents; and (ii) self-expandable stents. Generally speaking, a stent delivery system includes the stent and some means for positioning and fixing the stent in place within a body lumen.
• A balloon-expandable stent is typically a ductile metal tube. The delivery system for such a stent typically includes an inflatable balloon secured to the distal end of a catheter, the balloon-expandable stent being secured to the catheter over the inflatable balloon. In use, the catheter is introduced to a desired site within a body lumen, and the balloon is expanded until the stent positioned thereover is inelastically expanded to its desired size against the walls of the lumen. The balloon is then deflated, and the catheter is withdrawn from the site, thereby leaving the expanded stent in place against the walls of the lumen. An example of a balloon-expandable stent and delivery system therefor is disclosed in U.S. Pat. No. 4,922,905, inventor Strecker, issued May 1990, the disclosure of which is incorporated herein by reference.
• A self-expandable stent is typically an elastic tube that self-expands after having been compacted. Illustrative examples of self-expandable stents are disclosed in the following documents, all of which are incorporated herein by reference: U.S. Pat. No. 5,876,445, inventors Andersen et al., issued Mar. 2, 1999; U.S. Pat. No. 5,366,504, inventors Andersen et al., issued Nov. 22, 1994; U.S. Pat. No. 5,234,457, inventor Andersen, issued Aug. 10, 1993; U.S. Pat. No. 5,061,275, inventors Wallsten et al., issued Oct. 29, 1991; Watkinson et al., “The Role of Self-Expanding Metallic Endoprostheses in Esophageal Strictures,”Seminars in Interventional Radiology,13(1):17-26 (March 1996); and Strecker et al., “Nitinol Esophageal Stents: New Designs and Clinical Indications,”Cadiovasc. Intervent. Radiol.,19:15-20 (1996).
• The delivery system for a self-expandable stent typically comprises a catheter and a restraint for temporarily holding the stent in a compressed state at the distal end of the catheter. In use, the catheter is introduced to a desired site within a body lumen, and the restraint is removed, thereby allowing the stent to expand by its own elastic restoring force against the walls of the lumen. One of the more common self-expandable stent delivery systems of the above-described type comprises a coaxial tube assembly. More specifically, said delivery system comprises an inner catheter and an outer catheter, said outer catheter being coaxial with said inner catheter. The inner and outer catheters are appropriately sized so that a stent inserted over the distal end of the inner catheter is maintained in a compressed state by the inner surface of the outer catheter. In use, the assembly is introduced to a desired site, and the outer catheter is axially retracted relative to the inner catheter, thereby allowing the stent to self-expand off the inner catheter and against the walls of the lumen.
• Illustrative examples of the aforementioned type of delivery system include the following U.S. patents, all of which are incorporated herein by reference: U.S. Pat. No. 5,484,444, inventors Braunschweiler et al., issued Jan. 16, 1996; U.S. Pat. No. 5,026,377, inventors Burton et al., issued Jun. 25, 1991; U.S. Pat. No. 4,990,151, inventor Wallsten, issued Feb. 5, 1991; and U.S. Pat. No. 4,732,152, inventors Wallsten et al., issued Mar. 22, 1988. A commercial embodiment of the above-described delivery system is the UNISTEP PLUS™ delivery system (Boston Scientific Corporation, Natick, Mass.).
• Although the above-described coaxial tube delivery system is well-suited for many types of self-expandable stents, such a delivery system is not particularly well-suited for those self-expandable stents that have limited axial strength, such as the Strecker stent—a knitted nitinol wire stent disclosed in U.S. Pat. No. 5,366,504 and commercially available from Boston Scientific Corporation, Natick, Mass. This is because such stents are often unable to resist becoming axially compressed during assembly of the coaxial tube delivery system, when the distal end of the outer catheter must be drawn across the stent, and/or during deployment of the coaxial tube delivery system, when the distal end of the outer catheter must be withdrawn across the stent.
• Consequently, alternative delivery systems have been devised for use with the Strecker stent and with other like stents of limited axial strength. One such system, which is exemplified by the ULTRAFLEX™ esophageal stent system (Boston Scientific Corporation, Natick, Mass.), comprises a stent of the aforementioned type, said stent being mounted on an inner catheter and being encased in a pharmaceutical grade dissolvable gelatin to maintain the stent in a compressed state. An outer catheter surrounds the gelatin-encased stent. In use, the system is inserted into a patient's esophagus and the outer catheter is retracted. Moisture present in the esophagus causes the restraining gelatin to dissolve, thereby allowing the stent to expand.
• Another delivery system devised for use with the Strecker stent and like stents of limited axial strength is disclosed in U.S. Pat. No. 5,405,378, inventor Strecker, which issued Apr. 11, 1995, and which is incorporated herein by reference. Said delivery system, which does not include an outer catheter, uses a crocheted suture cord to compress the stent against a catheter core. The crocheted cord is connected to a finger ring at the proximal end of the delivery system. Retraction of the finger ring unravels the cord in a circular manner down the length of the stent, gradually deploying the stent. A commercial embodiment of the aforementioned delivery system is the COVERED ULTRAFLEX™ esophageal stent system (Boston Scientific Corporation, Natick, Mass.).
• Unfortunately, the manufacture of the aforementioned crocheted cord delivery system is typically performed manually and can be quite taxing physically as a great deal of strength is required to tightly stretch the stent down on the catheter while crocheting the cord around the stent. Another problem with the foregoing system is that, during deployment, the crocheted cord does not always unravel correctly and completely.
SUMMARY
• It is an object of the present invention to provide a novel stent delivery system.
• It is another object of the present invention to provide a stent delivery system as described above that overcomes at least some of the above-described shortcomings associated with existing stent delivery systems.
• It is still another object of the present invention to provide a stent delivery system that has a minimal number of parts, that can be mass-produced, that is easy to manufacture and that is easy to use.
• Therefore, in furtherance of the above and other objects to be described or to become apparent from the description below, there is provided herein a stent delivery system constructed according to the teachings of the present invention, said stent delivery system comprising, in one embodiment, (a) an inner catheter; (b) an outer catheter, said outer catheter surrounding at least a portion of the length of said inner catheter and adapted for axial movement relative to said inner catheter; (c) a self-expandable stent disposed between said inner catheter and said outer catheter; and (d) a stent restraining member disposed between said outer catheter and said self-expandable stent, said stent restraining member being dimensioned to maintain said self-expandable stent in a compressed state.
• The aforementioned stent restraining member may be a braided tube (or any other type of tube) surrounding said self-expandable stent, said braided tube preferably being made from a strong, flexible, filamentary material having a low coefficient of friction. Examples of such materials may be a fine polyester or metal wire. The braided tube may be formed directly over the stent, preferably using an automated braiding machine, or may be pre-formed and then inserted over the stent. Where the braided tube is pre-formed and inserted over the stent, the system preferably further includes a braid holding sleeve secured to the inner catheter, said braid holding sleeve being adapted to receive the proximal end of the braided tube. The distal end of the stent restraining member is preferably mechanically coupled to the distal end of the outer catheter so that retraction of the outer catheter causes the stent restraining member to retract from the stent, thereby allowing the stent to self-expand.
• Instead of being a tube, the stent restraining member may be a coil helically wrapped around the stent, said coil preferably being made from a strong, flexible, wire-like, thread-like or ribbon-like material having a low coefficient of friction.
• The self-expandable stent is preferably a knitted mesh of nitinol wire flexible in both the radial and longitudinal axes, said stent preferably being coaxially positioned relative to the inner catheter and being stretched longitudinally thereacross.
• The outer catheter may be a solid tube or may be a tube having a longitudinal split extending proximally from its distal end at least partially along its length. Where the outer catheter has a longitudinal split, said split is preferably sealed after the outer catheter has been advanced over and secured to the stent restraining member.
• The stent delivery system preferably further comprises means for deterring said self-expandable stent from sliding proximally relative to said inner catheter during deployment, said deterring means further comprising a stent engaging sleeve fixed to said inner catheter, said self-expandable stent surrounding said stent engaging sleeve, said stent engaging sleeve having an outer surface adapted to engage said self-expandable stent in such a way as to deter said self-expandable stent from sliding proximally relative thereto.
• In another embodiment, the stent delivery system of the present invention comprises (a) an inner catheter; (b) an outer catheter, said outer catheter surrounding at least a portion of the length of said inner catheter and adapted for axial movement relative to said inner catheter; and (c) a self-expandable stent disposed between said inner catheter and said outer catheter, said self-expandable stent being flexible in both the radial and longitudinal axes, said self-expandable stent being held in a compressed state by said outer catheter.
• The aforementioned self-expandable stent is preferably a knitted mesh of nitinol wire coaxially mounted on said inner catheter. The outer catheter preferably has a longitudinal split extending proximally from its distal end at least partially along its length, said split preferably being sealed after the outer catheter has been advanced over and secured to the stent restraining member.
• The stent delivery system preferably further comprises means for deterring said self-expandable stent from sliding proximally relative to said inner catheter during deployment, said deterring means further comprising a stent engaging sleeve fixed to said inner catheter, said self-expandable stent surrounding said stent engaging sleeve, said stent engaging sleeve having an outer surface adapted to engage said self-expandable stent in such a way as to deter said self-expandable stent from sliding proximally relative thereto.
• The present invention is also directed to a method of manufacturing a stent delivery system, said method comprising, in one embodiment, the steps of (a) providing an inner catheter; (b) compressing a self-expandable stent over said inner catheter; (c) while said self-expandable stent is in a compressed state, positioning a braided tube around said inner catheter and said self-expandable stent, said braided tube being dimensioned to maintain said self-expandable stent in said compressed state; and (d) positioning an outer catheter around said braided tube, said outer catheter being adapted for axial movement relative to said inner catheter.
• The aforementioned braided tube positioning step may comprise forming a braided tube over said self-expandable stent and said inner catheter or may comprise pre-forming a braided tube and then sliding said pre-formed braided tube over said stent and said inner catheter.
• The stent and the inner catheter are preferably coaxially disposed, with said stent being flexible in both the longitudinal and radial axes. The aforementioned compressing step preferably comprises stretching said stent longitudinally across the length of said inner catheter.
• Preferably, said method further comprises mechanically coupling said outer catheter to said braided tube for axial movement. The outer catheter may be a solid tube or may be a tube provided with a longitudinal slit extending at least a part of the length thereof. In the case of the tube with a longitudinal slit, the method preferably further comprises, after said outer catheter positioning step, the step of sealing said longitudinal slit.
• The above method preferably further comprises, before said compressing step, the step of fixing a stent engaging sleeve to said inner catheter, said self-expandable stent surrounding said stent engaging sleeve, said stent engaging sleeve having an outer surface adapted to engage said self-expandable stent in such a way as to deter said self-expandable stent from sliding proximally relative thereto. In addition, said method preferably also comprises, before said outer catheter positioning step, the steps of fixing a braid holding sleeve to said inner catheter and securing the proximal end of said braided tube to said braid holding sleeve.
• In another embodiment, the method of the present invention comprises the steps of (a) providing an inner catheter; (b) compressing a self-expandable stent over said inner catheter; (c) while said self-expandable stent is in a compressed state, wrapping a helical restraint around said inner catheter and said self-expandable stent, said helical restraint being dimensioned to maintain said self-expandable stent in said compressed state; and (d) positioning an outer catheter around said helical restraint, said outer catheter being adapted for axial movement relative to said inner catheter.
• The aforementioned helical restraint is preferably made from a strong, flexible filamentary or ribbon-like material having a low coefficient of friction. Preferably, said method further comprises mechanically coupling said outer catheter to said braided tube for axial movement. The outer catheter is preferably a tube provided with a longitudinal slit extending at least a part of the length thereof, the method preferably further comprising, after said outer catheter positioning step, the step of sealing said longitudinal slit.
• The subject method preferably still further comprises, before said compressing step, the step of fixing a stent engaging sleeve to said inner catheter, said self-expandable stent surrounding said stent engaging sleeve, said stent engaging sleeve having an outer surface adapted to engage said self-expandable stent in such a way as to deter said self-expandable stent from sliding proximally relative thereto.
• In still another embodiment, the method of the present invention comprises the steps of (a) providing an inner catheter; (b) compressing a self-expandable stent over said inner catheter, said self-expandable stent being flexible in both the radial and longitudinal axes; and (c) positioning an outer catheter around said self-expandable stent, said outer catheter being adapted for axial movement relative to said inner catheter and being dimensioned to maintain said self-expandable stent in a compressed state.
• Preferably, the aforementioned stent is a knitted mesh of nitinol wire. In addition, the outer catheter is preferably provided with a longitudinal slit extending at least a part of the length thereof, said method further comprising, after said outer catheter positioning step, the step of sealing said longitudinal slit.
• The subject method preferably further comprises, before said compressing step, the step of fixing a stent engaging sleeve to said inner catheter, said self-expandable stent surrounding said stent engaging sleeve, said stent engaging sleeve having an outer surface adapted to engage said self-expandable stent in such a way as to deter said self-expandable stent from sliding proximally relative thereto.
• Additional objects, features, aspects and advantages of the present invention will be set forth, in part, in the description which follows and, in part, will be obvious from the description or may be learned by practice of the invention. In the description, reference is made to the accompanying drawings which form a part thereof and in which is shown by way of illustration specific embodiments for practicing the invention. These embodiments will be described in sufficient detail to enable those skilled in the art to practice the invention, and it is to be understood that other embodiments may be utilized and that structural changes may be made without departing from the scope of the invention. The following detailed description is, therefore, not to be taken in a limiting sense, and the scope of the present invention is best defined by the appended claims.
BRIEF DESCRIPTION OF THE DRAWINGS
• The accompanying drawings, which are hereby incorporated into and constitute a part of this specification, illustrate preferred embodiments of the invention and, together with the description, serve to explain the principles of the invention. In the drawings wherein like reference numerals represent like parts:
• FIG. 1 is a side view of a first embodiment of a stent delivery system constructed according to the teachings of the present invention;
• FIG. 2 is a fragmentary schematic longitudinal section view of the stent delivery system ofFIG. 1, showing the distal end thereof;
• FIG. 3 is a schematic transverse section view of the stent delivery system ofFIG. 1 taken along line1-1;
• FIG. 4 is an enlarged perspective view of the stent engaging sleeve of the stent delivery system ofFIG. 1;
• FIG. 5 is a side view of the stent of the stent delivery system ofFIG. 1, the stent being shown in a relaxed, expanded state;
• FIG. 6 is an enlarged perspective view of the stent restraining sleeve of the stent delivery system ofFIG. 1;
• FIG. 7 is a schematic fragmentary side view illustrating the manner in which the stent restraining sleeve of the stent delivery system ofFIG. 1 may be formed over the stent thereof by a rolling braid technique;
• FIG. 8 is a fragmentary schematic longitudinal section view of a second embodiment of a stent delivery system constructed according to the teachings of the present invention;
• FIG. 9 is a schematic fragmentary longitudinal section view of the distal end of the stent delivery system ofFIG. 1, illustrating the system during stent deployment;
• FIG. 10 is a schematic fragmentary longitudinal section view of a third embodiment of a stent delivery system constructed according to the teachings of the present invention;
• FIG. 11 is a schematic transverse section view of the stent delivery system ofFIG. 10;
• FIG. 12 is schematic fragmentary longitudinal section view of a fourth embodiment of a stent delivery system constructed according to the teachings of the present invention;
• FIG. 13 is a schematic transverse section view of the stent delivery system ofFIG. 12;
• FIG. 14 is a side view of a fifth embodiment of a stent delivery system constructed according to the teachings of the present invention;
• FIG. 15 is a schematic transverse section view of the stent delivery system ofFIG. 14 taken along line2-2; and
• FIG. 16 is a schematic longitudinal section view of a sixth embodiment of a stent delivery system constructed according to the teachings of the present invention.
DETAILED DESCRIPTION OF PREFERRED EMBODIMENTS
• Referring now toFIGS. 1 through 3, there are shown various views of a first embodiment of a stent delivery system constructed according to the teachings of the present invention, said stent delivery system being represented generally byreference numeral11.
• System11 comprises a flexible,inner catheter13. Ahandle15 is disposed at the proximal end ofcatheter13, and anenlarged tip17 is disposed at the distal end ofcatheter13. Alumen19 extends longitudinally throughcatheter13,lumen19 being adapted to receive a guide wire for use inpositioning system11 at a desired position within a body lumen.
• System11 further comprises astent engaging sleeve21,sleeve21 coaxially surrounding and secured (e.g., by a frictional fit) to that portion ofcatheter13 proximally contiguous totip17. The primary purpose ofsleeve21 is to engage a stent mounted thereover in such a way as to prevent said stent, during deployment, from sliding proximally relative tocatheter13. To this end, as can be seen inFIG. 4, the outer surface ofsleeve21 is provided with a plurality ofprojections23 adapted to engage the mesh-like structure of a stent in such a way as to restrain axial movement of the stent. Although, in the embodiment shown,projections23 are in the form of bumps, it can readily be appreciated thatprojections23 may take a variety of shapes including, but not limited to, ridges, hooks, threads, pegs, etc. Alternatively,sleeve21 may be provided with a roughened surface, such as that of sandpaper, to increase the coefficient of friction between the stent andsleeve21 and, thereby, to restrain axial movement of the stent during deployment. In still another alternative embodiment,sleeve21 may be made of a soft, compressible material, such as silicone, so that a stent mounted thereover becomes partially embedded therein and cannot easily slide proximally relative thereto during deployment.
• Referring back toFIGS. 2 and 3,system11 additionally comprises a self-expandable stent31 (shown separately inFIG. 5). Although, in the present embodiment,stent31 is a self-expandable stent of the type comprising a knitted mesh of nitinol (a nickel/titanium alloy) wire flexible in both the radial and longitudinal axes,stent31 is not so limited and may be virtually any type of self-expandable stent. A preferred example ofstent31 is the ULTRAFLEX™ Strecker esophageal stent—a self-expandable stent comprising a knitted mesh of 0.15 inch nitinol wire flexible in both the radial and longitudinal axes. Said ULTRAFLEX™ Strecker esophageal stent has a length of 7 cm, 10 cm or 15 cm and an expanded diameter of 18 mm, the proximal end of the stent forming a 5mm collar32 having an expanded diameter of 20 mm.
• Stent31 is mounted oversleeve21 in a stretched or compressed state and is maintained, until deployment, in said stretched or compressed state in the manner to be described below.
• System11 further comprises a stent restraining sleeve41 (shown separately inFIG. 6).Sleeve41 coaxially surroundsstent31 and is appropriately sized to maintainstent31 in its stretched state. In the present embodiment,sleeve41 is a braided tube, said braided tube preferably being made from a wire or filament that is strong, flexible and has a low coefficient of friction. Said wire or filament may be made of a fine polyester, metal or like material.
• In the present embodiment,sleeve41 is formed directly overstent31 in the following manner: First, as shown inFIG. 7,stent31 is stretched tightly oversleeve21 andcatheter13. This may be done by looping or hooking proximal and distal strings PS and DS, respectively, onto the proximal and distal ends, respectively, ofstent31 and then by tightly pulling proximal strings PS proximally and distal strings DS distally, either manually or using a motorized pulling mechanism, untilstent31 is fully stretched. In its stretched state,stent31 may have a diameter of about 5-6 mm, as compared to a diameter of 18-20 mm in its expanded or un-stretched state. Adhesive tape T or the like is then used to secure proximal strings PS and distal strings DS tocatheter13 in their pulled-apart states to maintainstent31 in its stretched configuration.
• Next, the above-described assembly is then passed through a wire braiding machine M in the direction indicated by arrow A, which formssleeve41 directly overstent31. Machine M may be a conventional wire braiding machine, such as Model 40/98 from Rotek Technologies, Inc. (Ormond Beach, Fla.), which is capable of braiding twenty wires or filaments. Aftersleeve41 has been formed, strings PS and DS and tape T are removed, leavingsleeve41 to restrainstent31 in its stretched state.
• Referring back now toFIGS. 1 through 3,system11 also comprises a flexible,outer catheter51,catheter51 coaxially surrounding much of the distal end ofcatheter13 up totip17.Catheter51 is adapted for axial movement relative tocatheter13, and ahandle53 is disposed at the proximal end ofcatheter51 for use in axially movingcatheter51 relative tocatheter13. In order to accommodatesleeve41,stent31 andsleeve21 betweencatheter51 andcatheter13, the distal end ofcatheter51 is provided with an increased inside diameter. Alternatively, instead of constructingcatheter51 to have an increased inside diameter at its distal end, there is shown inFIG. 8 asystem11′ comprising anouter catheter51′ of constant inside diameter,system11′ further comprising a space-fillingjacket61 secured (e.g., by a friction-fit) tocatheter13 proximally relative tosleeve21.Jacket61 serves to prevent proximal sliding ofstent31 andsleeve21 during deployment and also serves to prevent buckling and/or kinking ofcatheter51′ during deployment.
• Referring back toFIGS. 2 and 3, the distal end ofcatheter51 is secured to the distal end ofsleeve41 by an adhesive52 so thatsleeve41 is mechanically coupled tocatheter51 for purposes of axial movement. (Instead of using adhesive52,catheter51 andsleeve41 may be coupled together using other mechanical means, such as a clamp, a cable-tie, pins or a crimp.) Due to the coupling together ofcatheter51 andsleeve41, retraction (i.e., proximal movement) ofcatheter51 relative tocatheter13 simultaneously results in the retraction ofsleeve41 relative tostent31.
• To facilitate the advancement ofcatheter51 oversleeve41 during the assembly ofsystem11,catheter51 is provided with alongitudinal split55 extending proximally from its distal end. The reason for providingsplit55 incatheter51 is to avoid having to slidecatheter51past sleeve41 and possibly dislodgingsleeve41 fromstent31. In the present embodiment, split55 extends proximally only partially from the distal end ofcatheter51; however, it can readily be appreciated that split55 could extend the entire length ofcatheter51. Aftercatheter51 has been properly positioned oversleeve41, adhesive52 is used to bond the distal ends ofcatheter51 andsleeve41, as described above, and is also used to sealsplit55. As can readily be appreciated, instead of sealing split55 with adhesive52, split55 could be welded together.
• In use,system11 is inserted into a body lumen and advanced to a desired site therewithin in the conventional fashion.System11 is then deployed by retracting (i.e., sliding proximally)catheter51 relative tocatheter13. As seen inFIG. 9, ascatheter51 is retracted,sleeve41 slides offstent31, thereby permittingstent31 to self-expand.Sleeve21 helps to ensure thatstent31 does not retract withsleeve41 andcatheter51.
• Referring now toFIGS. 10 and 11, there are shown longitudinal and transverse section views, respectively, of a third embodiment of a stent delivery system constructed according to the teachings of the present invention, said stent delivery system being represented generally byreference numeral101.
• System101 is similar in most respects tosystem11, the principal difference between the two systems being thatsystem101 does not includesleeve41 ofsystem11. Instead,system101 relies oncatheter51 to function as the external restraint mechanism for keepingstent31 in its compressed state until deployment. A lubricant (not shown) may be applied to the inside surface ofcatheter51 to ensure thatstent31 does not axially compress, during deployment, ascatheter51 is moved proximally. As can readily be appreciated,catheter51 ofsystem101 could be replaced withcatheter51′ andjacket61.
• System101 is used in the same manner assystem11.
• Referring now toFIGS. 12 and 13, there are shown longitudinal and transverse section views, respectively, of a fourth embodiment of a stent delivery system constructed according to the teachings of the present invention, said stent delivery system being represented generally byreference numeral201.
• System201 is similar in most respects tosystem11, the principal difference between the two systems being thatsystem201 comprises, instead ofsleeve41, a stent restraining element in the form of a singlehelical coil203 wrapped aroundstent31.Coil203 may be made of wire, thread, ribbon or like materials and may be wrapped aroundstent31 either manually or with the use of an automated winding machine. The distal end ofcoil203 is coupled to the distal end ofcatheter51. One advantage to usingcoil203, instead ofsleeve41, is that it is less complicated and less costly, particularly in terms of automated equipment, to apply a single, coiled constrainment element than it is to apply multiple elements in the form of a braid. As can readily be appreciated,catheter51 ofsystem201 could be replaced withcatheter51′ andjacket61.
• System201 is used in the same manner assystem11.
• Referring now toFIGS. 14 and 15, there are shown side and transverse section views, respectively, of a fifth embodiment of a stent delivery system constructed according to the teachings of the present invention, said stent delivery system being represented generally byreference numeral301.
• System301 is similar in most respects tosystem11, the principal difference between the two systems being thatsystem301 includes a flexibleouter catheter303 that is identical tocatheter51, except thatcatheter303 is not fabricated with a longitudinal split. The distal end ofcatheter303 is mechanically coupled to the distal end ofsleeve41. As can readily be appreciated,catheter51 ofsystem301 could be replaced withcatheter51′ andjacket61.
• System301 is used in the same manner assystem11.
• Referring now toFIG. 16, there is shown a longitudinal section view of a sixth embodiment of a stent delivery system constructed according to the teachings of the present invention, said stent delivery system being represented generally byreference numeral401.
• System401 is similar in many respects tosystem11. One difference between the two systems is thatsystem401 includes abraided sleeve403 that, instead of being fabricated directly on top of stent31 (as in the case of sleeve41), is separately fabricated and is then slid over stretchedstent31. The inner diameter ofsleeve403 is preferably made to be slightly greater than the outer diameter ofstent31 in a stretched-out state so thatsleeve403 can be easily slid over stretched-out stent31 while still being capable of retaining stent in said stretched-out state. Another difference between the two system is thatsystem401 includes a flexibleouter catheter405,catheter405 being identical tocatheter303. The distal end ofcatheter405 is mechanically coupled to the distal end ofsleeve403. Still another difference between the two systems is thatsystem401 further includes asleeve holding member407.Member407, which is secured tocatheter13, preferably by a friction fit, is adapted to securely receive the proximal end ofsleeve403 in such a way as to preventsleeve403 from sliding distally ascatheter405 is advanced oversleeve403. As can readily be appreciated,catheter51 ofsystem401 could be replaced withcatheter51′ andjacket61.
• System401 is used in the same manner assystem11.
• The embodiments of the present invention recited herein are intended to be merely exemplary and those skilled in the art will be able to make numerous variations and modifications to it without departing from the spirit of the present invention. All such variations and modifications are intended to be within the scope of the present invention as defined by the claims appended hereto.

Claims (20)

What is claimed is:

1. A stent delivery system, comprising:

an outer elongate shaft having a lumen;

an inner elongate shaft extending through the lumen of the outer elongate shaft;

a stent engaging sleeve surrounding a distal region of the inner elongate shaft; and

a self-expandable stent surrounding the stent engaging sleeve and positioned within the lumen of the outer elongate shaft in a compressed state, the self-expandable stent including a wire mesh;

wherein the wire mesh of the self-expandable stent is embedded into the stent engaging sleeve in the compressed state.

2. The stent delivery system ofclaim 1, wherein the stent engaging sleeve is formed of a soft, compressible material.

3. The stent delivery system ofclaim 1, wherein the stent engaging sleeve is formed of a soft, compressible silicone material.

4. The stent delivery system ofclaim 1, wherein the outer elongate shaft is configured to longitudinal slide relative to the inner elongate member to deploy the self-expandable stent.

5. The stent delivery system ofclaim 4, wherein the stent engaging sleeve prevents relative longitudinal sliding movement between the self-expandable stent and the inner elongate shaft during deployment of the self-expandable stent.

6. The stent delivery system ofclaim 1, wherein the stent engaging sleeve extends from a proximal end of the self-expandable stent to a distal end of the self-expandable stent.

7. The stent delivery system ofclaim 1, wherein the self-expandable stent is longitudinally stretched in the compressed state.

8. The stent delivery system ofclaim 7, wherein in the compressed state the self-expandable stent has a diameter of 5 to 6 mm.

9. The stent delivery system ofclaim 8, wherein the self-expandable stent is expandable to an expanded state, wherein the self-expandable stent has a diameter of 18 to 20 mm in the expanded state.

10. The stent delivery system ofclaim 1, further comprising an outer sleeve surrounding the self-expandable stent.

11. The stent delivery system ofclaim 10, wherein the outer sleeve is a braided tube.

12. The stent delivery system ofclaim 10, wherein the outer sleeve is secured to the outer elongate shaft.

13. The stent delivery system ofclaim 10, wherein a distal end of the outer sleeve is secured to a distal end of the outer elongate shaft with an adhesive.

14. The stent delivery system ofclaim 1, wherein the outer elongate shaft includes a longitudinal slit extending proximally from a distal end of the outer elongate shaft.

15. A stent delivery system, comprising:

an outer elongate shaft having a lumen extending therethrough;

an inner elongate shaft extending through the lumen of the outer elongate shaft, the inner elongate shaft including an enlarged distal tip positioned distal of a distal end of the outer elongate shaft;

a stent engaging sleeve surrounding a distal region of the inner elongate shaft proximal of the enlarged distal tip, the stent engaging sleeve formed of a soft, compressible material; and

a self-expandable stent surrounding the stent engaging sleeve and positioned within the lumen of the outer elongate shaft in a compressed state, the self-expandable stent including a knitted wire mesh;

wherein the knitted wire mesh of the self-expandable stent is embedded into the stent engaging sleeve in the compressed state.

16. The stent delivery system ofclaim 15, wherein the knitted wire mesh is longitudinally stretched in the compressed state.

17. The stent delivery system ofclaim 15, wherein the outer elongate shaft is configured to longitudinal slide relative to the inner elongate member to deploy the self-expandable stent, and wherein the stent engaging sleeve prevents relative longitudinal sliding movement between the self-expandable stent and the inner elongate shaft during deployment of the self-expandable stent.

18. The stent delivery system ofclaim 1, wherein the stent engaging sleeve extends from a proximal end of the self-expandable stent to a distal end of the self-expandable stent.

19. The stent delivery system ofclaim 18, wherein a distal end of the stent engaging sleeve is positioned adjacent to the enlarged distal tip.

20. The stent delivery system ofclaim 15, further comprising an outer sleeve surrounding the self-expandable stent to retain the self-expandable stent in the compressed state.

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