Classifications

• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61F—FILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
  • A61F2/00—Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
  • A61F2/95—Instruments specially adapted for placement or removal of stents or stent-grafts
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61F—FILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
  • A61F2/00—Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
  • A61F2/82—Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
  • A61F2002/826—Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents more than one stent being applied sequentially
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61F—FILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
  • A61F2/00—Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
  • A61F2/95—Instruments specially adapted for placement or removal of stents or stent-grafts
  • A61F2/962—Instruments specially adapted for placement or removal of stents or stent-grafts having an outer sleeve
  • A61F2/966—Instruments specially adapted for placement or removal of stents or stent-grafts having an outer sleeve with relative longitudinal movement between outer sleeve and prosthesis, e.g. using a push rod
  • A61F2002/9665—Instruments specially adapted for placement or removal of stents or stent-grafts having an outer sleeve with relative longitudinal movement between outer sleeve and prosthesis, e.g. using a push rod with additional retaining means

Definitions

• This invention relates generally to medical apparatus and methods, and more specifically to vascular catheters, stents and stent delivery catheters for deployment in the coronary arteries and other vessels.
• Stenting has become an increasingly important treatment option for patients with coronary artery disease. Stenting involves the placement of a tubular prosthesis within a diseased coronary artery to maintain the patency of the artery, typically after a primary treatment such as angioplasty.
• a primary treatment such as angioplasty.
• restenosis i.e., the tendency of the coronary artery to become re-occluded following stent placement.
• restenosis rates have decreased substantially, due in part to drug coatings and other improvements in stent technology.
• the number of stent related procedures being performed in the United States, Europe, and elsewhere has increased dramatically.
• Stents are delivered to the coronary arteries using long, flexible vascular catheters typically inserted through a femoral artery.
• the stent is simply released from the delivery catheter and it resiliently expands into engagement with the vessel wall.
• a balloon on the delivery catheter is expanded which expands and deforms the stent to the desired diameter, whereupon the balloon is deflated and removed.
• a highly conformable (i.e. flexible) stent delivery catheter is desirable because such a catheter can bend and conform to the vessels of the human body.
• Diseased patients can have swollen or edematous tissues which can decrease the size of blood vessels used to access a lesion to be treated, thereby making access to a treatment region difficult.
• prosthetic stent segments must be delivered through lesions which can occlude, at least partially and in some instances substantially, a vessel in which the prosthetic stent is delivered, illustrating the importance of profile and conformability.
• the size, profile and conformity of a deployment catheter can effect the success in accessing a lesion site.
• the invention generally provides for the delivery of stent segments with a low profile catheter which is flexible and conformable, especially the distal end.
• the low profile and conformable delivery catheter permits deployment of a selected number of the stent segments at a single site, thus permitting in situ customization of stent length to better match the length of the lesion being treated.
• the delivery catheter has a simplified design which grip structure for separating the selected group of stent segments prior to deployment.
• the invention comprises an apparatus for implanting prosthetic segments in a body lumen with a carrier, typically an elongated flexible carrier positionable in the body lumen.
• a carrier typically an elongated flexible carrier positionable in the body lumen.
• Such carriers are exemplified by conventional coronary, cerebral, and peripheral catheters of the type well described in the medical and patent literature.
• a plurality of prosthetic segments are axially distributed on an exterior surface of the carrier.
• the prosthetic segments are releasably secured or otherwise positioned on the exterior surface of the carrier so that they may be deployed in situ within the target body lumen.
• a separator is advanced distally over the segments and retracted proximally to separate a proximal group of the segments from a distal group of the segments. The separated distal group of segments can then be delivered into the body lumen while the remaining proximal stent segments remain constrained within the separator as described in detail below.
• the selected distal group of prosthetic segments will be deployed by application of a radially outward internal force.
• the carrier comprises a catheter having an expandable member, typically an inflatable balloon.
• the expandable member provides the exterior surface which carries the plurality of prosthetic segments, and in an exemplary embodiment has a length in the range from 1 cm to 20 cm, and is expandable to a diameter in the range from 1 mm to 5 mm.
• the apparatus for implanting prosthetic segments of the present invention may further comprise a constraining tube or other structure which is positionable over the inflatable balloon or other expandable member of the elongated flexible carrier.
• the constraining tube will have dimensions selected so that it can constrain or inhibit inflation of the balloon or expansion of other type of expandable member so that the length of expansion of the expandable member can be controlled.
• the constraining tube may form part of or otherwise be provided by the same structure as the separator which is used to separate proximal segments from distal segments, as described in more detail below.
• the apparatus can include any number of prosthetic segments, for example from 2 to 50, usually from 2 to 30, and typically from 5 to 20 prosthetic segments carried by the expandable member.
• the prosthetic segments can have interleaved ends prior to axial separation, as described in co-pending, commonly assigned application serial number 10/736,666, filed on December 16, 2003, the disclosure of which is incorporated fully herein by reference. Such interleaved ends permit the segments to be packed closely on the earner and provide a greater density of deployed prosthetic stent segments.
• the prosthetic segments typically each have a length in the range from 2 mm to 20 mm, more typically from 2 mm to 10 mm, and preferably from 4 mm to 8 mm.
• the separator comprises a separator tube having a distal end, a proximal end, a central passage, and an engagement member near the distal end thereof.
• the engagement member usually includes a grip structure which directly engages the distal most stent segment of the proximal group to be separated.
• the grip structure may be designed and fabricated so that it moves relatively freely over the plurality of stents as the separator tube is moved distally., but engages an adjacent stent segment when the separator tube is drawn proximally.
• Such grip structures which preferentially engage and apply a force to the adjacent stent segment are referred to hereinafter as "one-way grip structures.” By that, it is meant that they preferentially act to engage the adjacent stent segment only when pulled proximally.
• Other grip structures could be provided which engage and apply an essentially equal force to the adjacent or underlying stent segments as the separator tube is moved in both directions. In such cases, however, it will be necessary to prevent the plurality of stent segments from being moved distally as the separator tube is advanced thereover in a distal direction.
• a nose cone or other distal structure may be provided on the elongated flexible carrier at a position immediately distal of the distal-most stent segment to prevent distal translation of the stent segments.
• the separator tube is advanced distally with the one-way grip structure passing over the stent segments, preferably exerting little or no force on the stent segments.
• the separator tube is retracted proximally, so that the one-way grip structure grips the distal most segment and draws the entire proximal group of segments proximally relative to the balloon or other exterior surface, thus separating the distal and proximal segment groups.
• the grip structure is typically spaced proximally from a distal end of the separator tube by a distance of about one-half to twice the length of a prosthetic segment, preferably being approximately equal to the length of a prosthetic segment.
• This setback of the grip structure provides a distal region of the separator tube, sometimes referred to hereinbelow as the "garage,” which will cover and constrain any portion of the distal -most stent segment which extends beyond the grip structure after separation of the proximal group of stent segments from the distal group of stent segments.
• the separator tube may comprise or otherwise provide all or a portion of the constraining tube referred to hereinbefore. The separator tube will be adapted to regularly restrain the retracted stent segments from expansion while the exposed distal segments are expanded.
• the one-way grip structure can include a multiplicity of radially inwardly extending resilient fingers, such as inclined resilient tabs formed in a metal ring. At least some of the fingers will usually be inclined proximally so that they will pass easily over the prosthetic segments as the separator tube is advanced distally but grip the adjacent segment when the separator tube is pulled proximally, thus acting as a "ratchet" mechanism.
• the one-way grip may include a balloon or other inflatable structure to permit selective engagement of the adjacent stent segment by inflation.
• the one-way grip is releasable so that the grip may be selectively engaged and released from the segments as the separator tube is advanced and/or retracted.
• the one-way grip could also include an inclined or conical surface.
• a conical surface which tapers proximally to pass over the segments while advancing in a distal direction, and then grip the segments when the separator tube is retracted proximally.
• a conical surface can be arranged so that a smaller diameter trailing edge can be advanced distally over the stent segments. When retracted proximally, the edge will engage the adjacent segment to draw all proximal segments back proximally.
• the invention comprises a method for delivering stent segments to a body lumen.
• a plurality of adjacent stent segments are introduced into the body lumen at or near a region to be treated.
• One or more distally positioned stent segments are selected for delivery to the body lumen. All of the stent segments which are located proximally of the selected stent segment(s) are axially separated from the distal stent segment(s). Any stent segments which are proximal to the selected stent segments are retracted proximally, usually simultaneously.
• the selected distal stent segment(s) are deployed after they have been separated from the proximally located stent segments.
• the plurality of adjacent stent segments are introduced into a blood vessel, for example to treat a lesion therein, typically following angioplasty or other primary interventional treatment.
• Angioplasty predilation
• post dilation of the lesion can be performed by the catheter balloon of the present invention in the same intervention.
• the plurality of adjacent stent segments usually includes at least 3 stent segments, typically at least 5 stent segments, and often at least 10 stent segments.
• at least some of the adjacent stent segments are usually unattached prior to separating, for example unattached from each other and/or unattached from a surface of an expandable member.
• At least some of the plurality of stent segments can be frangibly (or in other cases permanently) attached prior to separation or could be interconnected by biodegradable links which could erode and detach after implantation.
• deployment of the stent is performed while imaging the lesion, the catheter, and/or the stents real time.
• the selection of the desired number of the stent segments can be performed under fluoroscopic imaging.
• the selection of the desired number of the stent segments can include aligning a marker disposed at or near the distal most stent segment with a distal end of a region to be treated and subsequently aligning a marker at or near the distal end of the separator tube with a proximal end of the lesion.
• the one-way grip or other engagement member is then properly aligned to separate a distal plurality of the stent segments having a length equal to that of the lesion. Inaccuracies resulting from imaging distortions, parallax errors, measurement errors, and/or catheter malpositioning are thus avoided.
• axial separation of the stent segments includes engaging the stent segment which is located immediately proximal of the selected segment(s) with a separator, and drawing the separator proximally.
• the separator can be a tube with a grip structure positioned near the distal end of the tube, and the grip structure is positioned over the immediately proximal stent segment to engage the immediately proximal stent segment.
• a deployment balloon or other expansible surface can be expanded to radially expand and deploy the selected stent segment(s).
• the proximally located stent segments are radially constrained, for example within the separator tube, while the selected stent segment(s) are radially expanded.
• the invention comprises a method for selectively delivering stent segments to a treatment region in a blood vessel.
• a balloon deployment catheter is positioned through the blood vessel to the treatment region, and a plurality of adjacent stent segments are positioned over the balloon.
• a separator tube is advanced over one or more proximally positioned stent segment(s), and a grip structure on the separator tube engages against a distal most of the proximally positioned stent segments. The separator tube is pulled proximally to separate the proximally positioned stent segments from the remaining distally positioned stent segment(s).
• the balloon is inflated to deploy the distally positioned stent segment(s) while the proximally positioned stent segments remain covered by the separator tube.
• the plurality usually includes at least 3 adjacent typically at least 5, and often at least 10 stent segments, and at least some of the plurality of stent segments are unattached prior to separation, so as to facilitate separation. Alternatively or in combination, at least some of the plurality of stent segments may be attached prior to separation to provide attached segments following deployment.
• the distal most stent segment can be aligned with the distal end of the region to be treated, and the grip structure engaged against a stent segment which lies immediately proximally of the proximal end of the region to be treated.
• the alignment can be performed with the aid of real time imaging, for example fluoroscopic imaging.
• the stents and other prosthetic segments of the present invention may be covered with drugs and bioactive agents, such as anti-restenotic agents as well described in the co-pending applications previously incorporated herein by reference.
• the prosthetic and stent segments could be formed from a shape or heat memory alloy and be self-expanding. In such cases, the stent segments could be carried on the inside surface of the constraining tube where the separator would be coaxially received within the restraining tube.
• stent and prosthetic segments could also be formed from bioresorbable materials, and would be useful in a wide variety of vascular and nonvascular body lumens.
• vascular body lumens include the coronary, peripheral, and cerebral vasculature.
• Non-vascular body lumens include the ureter, urethra, fallopian tubes, spinal column, and the like.
• Fig. IA shows a perspective view of a stent delivery catheter with an outer separator tube retracted and an expandable member inflated, in accordance with the present invention.
• Fig. IB shows a fully retracted separator, exposed prosthetic segments disposed over an expandable member, and a one-way grip structure in accordance with and embodiment.
• Figs. 2A-2D show deployment of selected prosthetic segments to treat a lesion in accordance with an embodiment.
• Fig. 3 A shows a one-way grip structure which includes a brake release.
• Fig. 3B shows a stent retention tube used to retain prosthetic segments.
• Fig. 4A shows a one-way grip structure which includes a deflectable flange or prong.
• Fig. 4B shows a one-way grip structure which includes an "L" shaped deflectable flange or prong.
• Fig. 4C shows a one-way grip structure which includes an annular inflatable balloon.
• Fig. 4D shows a one-way grip structure which includes a unilateral inflatable balloon.
• Fig. 4E shows a one-way grip structure which includes a flange or O-Ring.
• Fig. 5 A shows a one-way grip structure which includes shape memory using a Ni/Ti cylinder or wire loop
• Fig. 5B shows a one-way grip structure which includes flexible saw teeth or threads.
• Fig. 5C shows a one-way grip structure which includes bristles, foam or fabric.
• Fig. 5D shows a one-way grip structure which includes a tapered flange.
• Fig. 6 shows a garage located at the end of the stent separator tube in which the garage includes one-way grip structures in accordance with an embodiment.
• Fig. 7 shows another garage located at the end of the stent separator tube in accordance with an embodiment .
• Fig. 8 shows a garage as in Fig. 7 having concave arcuate cutouts on the ends of rectangular flanges which engage the prosthetic segments.
• FIGs. 9 A and 9B show plan and perspective views of a one-way grip structure with an arcuate flange in accordance with an embodiment.
• a stent delivery catheter 20 includes an elongated flexible carrier, such as a catheter body 22, an inner inflation shaft 27, or a separator tube 25 slidably disposed over the inner inflation shaft 27 (Fig. IB).
• Inner shaft 27 includes a lumen which is fluidly connected to inflatable member 24.
• a guidewire tube 34 is slidably positioned through a guidewire tube exit port 35 in separator tube 25 proximal to expandable member 24.
• Guidewire tube 34 extends through the interior of expandable member 24, the distal end of which is sealingly attached to guidewire tube 34.
• the proximal end of expandable member 24 is sealingly affixed around guidewire tube 34 and inner shaft 27.
• a tapered nosecone 28, typically composed of a soft elastomeric material, is mounted to guidewire tube 34 distally of expandable member 24 to reduce trauma to the vessel during advancement of the device.
• a prosthesis 30, which comprises a plurality of separate or separable prosthetic segments 32, is disposed on expandable member 24 for expansion therewith.
• a guidewire 36 is positioned slidably through guidewire tube 34, expandable member 24, and nosecone 28 and extends distally thereof.
• a handle 38 is attached to aproximal end 23 of catheter body 22. Handle 38 performs several functions, including advancing and retracting the separator tube, connecting a balloon inflation source, manipulating the catheter, etc.
• Various embodiments of a preferred handle and additional details concerning its structure and operation are described in co-pending United States Patent Application Serial No. 11/148,713, filed June 8, 2005, (Attorney Docket No. 14592.4002), entitled “Devices and Methods for Operating and Controlling Interventional Apparatus," which application has been previously incorporated herein by reference.
• Embodiments of another preferred handle and details concerning its structure and operation are described in co-pending United States Publication No.
• Handle 38 includes a housing 39 that encloses the internal components of the handle.
• Inner shaft 27 is preferably fixed to the handle, while separator tube 25 is able to be retracted and advanced relative to the handle 38.
• An adaptor 42 is attached to handle 38 at its proximal end, and is fluidly coupled to inner shaft 27 in the interior of the housing of handle 38.
• Adaptor 42 is configured to be fluidly coupled to an inflation device, which may be any commercially available balloon inflation device such as those sold under the trade name "IndeflatorTM", available from Guidant Corp. of Santa Clara, Calif.
• the adaptor is in fluid communication with expandable member 24 via an inflation lumen in inner shaft 27 to enable inflation of expandable member 24.
• Separator tube 25 and guidewire 36 each extend through a slider assembly 50 located on the catheter body 22 at a point between proximal and distal ends of the catheter body.
• Slider assembly 50 is adapted for insertion into and sealing within a hemostatic valve (not shown), such as on an introducer tube or guiding catheter, while allowing relative movement of separator tube 25 relative to slider assembly 50.
• Slider assembly 50 includes a slider tube 51, a slider body 52, and a slider cap 53.
• Separator tube 25 includes an engagement member 58, such as a one-way grip structure 62.
• a distal region 54 of the separator tube defines a garage for covering and constraining a portion of a prosthetic segment which extends beyond the grip 62 after separation.
• Separator tube 25 and engagement member 58 may be advanced toward nosecone 28 in a distal direction relative to expandable member 24 and stent segments 32.
• Each of the stent segments 32 has an axial length, typically from 1 mm to 50 mm, usually about 2 mm to 20 mm, and preferably about 3 mm to 10 mm.
• Grip structure 62 is typically located within a distance C relative to distal end 57, where C is typically from one-half to twice the stent segment length, more preferably from about one to 1.5 times the segment length. In exemplary embodiments C will be about 3 mm to 10 mm, with longer lengths being associated with longer segment lengths. Grip structure 62 contacts and engages stent segments 32.
• a distal portion 54 of separator tube 25 has a high circumferential strength, or hoop strength, such that the distal portion of the separator tube is able to prevent the expandable member 24 from expanding when the separator tube is extended over expandable member 24.
• the distal portion 54 of the separator tube 25 is preferably formed from metal or a polymer reinforced with a metallic or polymeric braid to resist radial expansion when expandable member 24 is expanded.
• Separator tube 25 may further have a liner surrounding its interior of lubricious or low friction material such as PTFE to facilitate relative motion of separator tube 25.
• the one-way grip structure 62 provides certain advantages. For example, a "oneway" grip structure can be designed to apply greater force when separator tube 25 is retracted proximally in order to reliably separate the stent segments without slippage.
• Radiopaque markers are preferably provided on the catheter to assist in positioning the catheter relative to the lesion and in selecting stent segments for deployment.
• a first radiopaque marker 56 (referred to as the "tube marker") is disposed at the distal end 57 of the separator tube 25 to facilitate visualization of the position of separator tube 25.
• a second radiopaque marker 60 is disposed on the inner shaft 27 near the distal end of expandable member 24. The second marker 60 may be referred to as the "balloon marker.”
• first marker 56 and second marker 60 will correspond to the length of prosthetic segments 32 which are exposed for deployment after the separator tube 25 has been drawn proximally to pull back the proximal groups of segments which are not being deployed.
• the physician can assure that the deployed prosthesis length closely matches the lesion length being treated. This is a particular advantage when the apparent lesion length is foreshortened due to the tortuosity and viewing angle in the fluoroscopic image.
• Grip structure 62 will usually be spaced proximally from distal end 57 of separator tube 25 by a distance sufficient to leave a distal "overhang” which will cover any portion of the distal most prosthetic segment which extends beyond the grip.
• grip structure 62 can be spaced proximally from distal end 57 a distance C approximately equal to axial length 31 of one of stent segments 32.
• each of stent segments 32 has the axial length of about 4 mm, and the grip structure 62 is located approximately 4 mm from distal end 57.
• grip structure 62 may be positioned at distal end 57 a distance or spaced proximally any distance up to twice or more times
• each of ten stent segments 32 can be deployed, and each of the ten stent segments can have an equal axial length 31.
• each of stent segments 32 are identical.
• Each of stent segments 32 can have interleaved ends in which a proximal end of a distal stent segment meshes with a distal end of an adjacent and proximally located stent segment as shown in Fig. IB. Such interleaving ensures adequate wall coverage and reduces or eliminates gaps between segments after deployment in the body lumen being treated.
• one-way grip structure 62 includes a necked-down circumferential waist or inwardly extending annular flange structure configured to frictionally engage stent segments 32 and thereby restrict the sliding movement of separator tube 25 relative to stent segments 32 when separator tube 25 is being retracted.
• One-way grip structure 62 may be a polymeric or metallic material integrally formed with separator tube 25 or may be bonded or otherwise mounted to the interior of the separator tube 25.
• one-way grip structure 62 may be toroidal with a circular or ovoid cross-section (like an O-ring) or the grip structure may have another cross-sectional shape such as triangular, trapezoidal, pyramidal, or other shape as described more fully herein below.
• Oneway grip structure 62 can be a polymer such as silicone or urethane sufficiently soft, compliant, and resilient to provide frictional engagement with stent segments 32, in some embodiments without damaging any coating deposited thereon.
• Grip structure 62 will extend radially inwardly a sufficient distance to engage the exterior of stent segments 32 with sufficient force to allow the line of stent segments 32 remaining within separator tube 25 to be retracted proximally with separator tube 25 so as to create spacing relative to those stent segments disposed distally of separator tube 25 for deployment.
• Any desired number of segments 32 can be used, and segments 32 may have a wide variety of lengths.
• balloon 24 has a length in the range from 60 mm to 65 mm, and up to fifteen 4 mm stent segments 32 can be deployed over a maximum deployment distance of up to 60 mm.
• up to ten 6 mm stent segments can be deployed over a maximum deployment distance of up to 60 mm.
• the stent segments can be crimped onto the expandable member 24 so that the expandable member carries the stent segments.
• the maximum deployment distance can be up to 200 mm or greater, and in further embodiments the inflatable member can be a tapered balloon to enhance stability of stent segments 32, particularly where lesion 70 is long.
• expandable member 24 can be tapered from an inflated outer diameter of 2.5 mm at its distal end to an outer diameter of about 3 mm at its proximal end.
• FIGs. 2 A-2D the deployment of selected prosthetic segments to treat a lesion is shown in accordance with an exemplary embodiment. While the embodiment will be described in the context of coronary artery treatment, it should be understood that the invention is useful in any of a variety of blood vessels and other body lumens in which stents are deployed, including the carotid, femoral, iliac and other arteries and veins, as well as nonvascular body lumens, such as the ureter, the urethra, fallopian tubes, the hepatic duct, and the like.
• a guiding catheter (not shown) is first inserted into a peripheral artery such as the femoral and advanced to the ostium of the right or left coronary artery.
• Guidewire 36 is then inserted through the guiding catheter and advanced into the target coronary artery 72 where a lesion 70 is to be treated.
• a region to be treated, for example lesion 70, is bounded by a proximal end 74 and a distal end 76.
• the proximal end of guidewire 36 is then inserted through nosecone 28 and guidewire tube 34 outside the patient's body and stent delivery catheter 20 is slidably advanced over guidewire 36 into the coronary artery.
• Slider assembly 50 is positioned within the hemostasis valve at the proximal end of the guiding catheter, which is then tightened to provide a hemostatic seal with the exterior of the slider body 52.
• Stent delivery catheter 20 is positioned through lesion 70 to be treated such that nosecone 28 is distal to lesion 70.
• Marker 60 is positioned near distal end 76 of lesion 70.
• separator tube 25 is retracted proximally so as to expose expandable member 24 and all of the stent segments 32 thereon as shown in Fig. 2 A.
• Use of the retracted separator tube during positioning of delivery catheter 20 can have the advantage of presenting a lower profile catheter to improve delivery to the lesion site, and presenting a highly flexible and conformable catheter in the distal portion of the catheter, which are particularly advantageous when passing through tortuous lumens.
• separator tube 25 is advanced distally over the segments until marker 56 is positioned near proximal end 74 of the treatment region so as to permit removal of a proximal group 82 of segments 32 which are not needed to treat lesion 70.
• a desired treatment distance corresponding to a desired number of deployed stent segments can be determined by a separation distance between the first marker 56 on separator tube 25 and second radiopaque marker 60 adjacent nose cone 28.
• oneway grip structure 62 advances over proximal stent segments 82.
• Distal stent segments 80 are located distal to one-way grip structure 62, and are selected for deployment based on the separation distance between the radiopaque markers.
• stent segments 32 may tend to flare outwardly at their proximal ends, which may hamper advancement of separator tube 25.
• the distal end of separator tube 25 may flare outwardly or may have an inner diameter that tapers in the proximal direction so as to present a larger diameter distal opening to receive stent segments 32 as the separator tube is advanced.
• separator tube 25 is retracted slightly to create a space between distal stent segments 80 and proximal stent segments 82.
• This space reduces the risk of dislodging or partially expanding the distal-most one of stent segments 82 when expandable member 24 is expanded.
• Retraction of separator tube 25 causes one-way grip structure 62 to grip and retract proximal stent segments 82 so as to separate proximal stent segments 82 from deployed stent segments 80. Deployed stent segments 80 are uncovered and remain adjacent to lesion 70.
• expandable member 24 is filled with fluid to expand radially so as to deploy distal stent segments 80. Radial expansion of deployed stent segments 80 urges deployed stent segments 80 outward against the vessel wall across lesion 70. Separator tube 25 constrains inflatable member 24 and prevents deployment of proximal stent segments 82. The number of stent segments 32 which are deployed will usually correspond to total stent or prosthesis lengths in the range from 4 to 200 mm. After stent segments 80 are deployed, inflatable member 24 is deflated and removed from deployed stent segments 80, leaving deployed stent segments 80 in a plastically-deformed, expanded configuration. Catheter 20 can then be removed and retracted from coronary artery 72.
• engagement member 58 includes a one-way grip structure 78 with a brake release 90 which holds stent segments 32 in place on expandable member 24 during introduction of the catheter 20 into a body lumen.
• the brake release 90 includes a pair of arms 92 which pivot about attachment pins 94.
• Each attachment pin 94 is coupled to a tubular slide 98 which slides over the inner inflation shaft 27.
• Arms 92 and pins 94 are mounted to move with slide 98, and grip structure 96 is disposed on separator tube 25. Proximal to the grip structure 96, the separator tube 25 has a proximal portion 97 with a reduced inner diameter.
• Advancement of the separator tube 25 causes the grip or wedge 96 to engage arm 92 which in turn pivots the arm about pin 94 to disengage the arm from the underlying shaft.
• the outer separator tube can be advanced by a desired distance to select a desired number of prosthetic or stent segments for deployment.
• the reduced inner diameter of the proximal portion of the separator tube 25 keeps arms 92 disengaged.
• separator tube is retracted proximally. Because arms 92 are disengaged from inner shaft 27, the slide 98 is able to move proximally as the separator tube 25 is retracted.
• the proximal segments are allowed to separate from the distal segments being deployed. The separated distal segments may then be deployed as described above.
• a stent retention tube 100 can be used to retain prosthetic segments 32 on an expandable member 24 during delivery to a treatment region.
• Stent retention tube 100 is disposed slidably over shaft 27 and within separator tube 25.
• Stent retention tube 100 has a distal end 101 that engages stent segments 32 and holds the segments in place relative to expandable member 24.
• Separator tube 25 can be advanced distally relative to the stent retention tube 100 in order to cover a desired number of stent segments which will not be deployed.
• the separator tube 25 and the stent retention tube 100 are together retracted proximally to separate deployed segments from proximal segments as described above.
• engagement member 58 can include a one-way grip structure 108 with a deflectable flange 110 or prong. Deflectable flange 110 extends inward to engage unused proximal stent segment(s) 82.
• Deflectable flange 110 is resilient and may be inclined proximally to pass over proximal stent segments 82 as the separator tube advances distally. Separator tube 25 is advanced distally as described above to select stent segments for deployment. Proximal retraction of separator tube 25 engages the most distal of the proximal stent segments 82 with deflectable flange 110, and the proximal stent segments are retracted as described above. [0061] Referring now to Fig. 4B, engagement member 58 can include a one-way grip structure 1 18 with a plurality of deflectable prongs 120 arranged around the inner circumference of separator tube 25. The resilient and deflectable prong bends proximally as separator tube 25 is advanced relative to stent segments 32.
• engagement member 58 can include a one-way grip structure 128 with an annular inflatable balloon 130.
• Annular balloon 130 is deflated and inflated using a lumen 132.
• annular balloon 130 is first deflated, or initially provided in a deflated state.
• Deflated annular balloon 130 is positioned over the distal most of the proximal stent segments to select stents for deployment as described above.
• Annular balloon 130 is inflated to engage the distal most of the proximal stent segments.
• Proximal retraction of separator tube 25 as described above retracts the proximal stent segments to separate the distal stent segments for deployment. The distal stent segments are then deployed as described above.
• engagement member 58 includes a one-way grip structure 138 with a unilateral inflatable balloon 140.
• Unilateral balloon 140 can be used in a manner similar to annular balloon 130 as described above.
• engagement member 58 can include a one-way grip structure 148 with a flange 150 or O-Ring.
• Flange 150 can be made from a polymeric material, or metal such as a Nickel / Titanium alloy as described above. Use of flange 150 is similar to other one-way engagement members described herein. For example, flange 150 can be moved distally to slide over and cover exposed segments as described above. Flange 150 frictionally engages stent segments 32 such that upon retraction, flange 150 separates the proximal segments from the deployed segments as described above.
• engagement member 58 can include a one-way grip structure 158 with a shape memory member structure comprising a Ni/Ti cylinder 160 surrounded by a heating coil 163. Voltage and/or current is applied to heating coil 163 with wires. Prior to application of voltage and/or current, cylinder 160 has a large diameter that may be positioned over segments 32. Application of voltage and/or current to heating coils 163 causes a Ni/Ti cylinder 160 to contract in diameter and engage segments 32. Separator tube 25 is retracted proximally to remove proximal segments and leave distal segments in position for deployment as described above.
• engagement member 58 can include a one-way grip structure 168 with flexible saw teeth 170 or threads.
• Flexible teeth 170 or threads can be rigid or flexible metal or polymer used in a manner similar to that described above with respect to the use of the flange.
• engagement member 58 can include a one-way grip structure 178 with bristles 180, or a foam or fabric material. Bristles 180, foam or fabric can be deployed in a manner similar to the flange described above.
• 5 engagement member 58 can include a one-way grip structure 188 with a tapered flange 190.
• Tapered flange 190 is tapered to have a smaller diameter at its proximal end and be suitable for one-way engagement of segments 32.
• engagement member 58 can include a garage 206 having a plurality of one-way grip structures 204 formed thereon.
• Each one-way grip structure 204 includes several resilient tabs 200, or fingers, which can be angled inward and proximally inclined to engage segments 32 as described above.
• Tabs 200 can include a repeating pattern of three adjacent fingers.
• Each tab can include a rounded end 232 to avoid damage to a coating on the engaged stent segment.
• Circular cutouts 220 can distribute forces from tabs 200 which are applied to adjacent region 202 to prevent tearing of the garage.
• a cross sectional size of circular cutouts 220 can be varied to provide resiliency and vary an amount of pressure which tabs 200 apply to the stent segments.
• Recesses 230 can be provided near rounded end 232 of the tabs 200. Recesses 230 can be provided on either side of rounded end 232 so as to define a pair of tips 233 along the lateral sides of the tabs 200. Tips 233 are adapted to engage the stent segments so as to keep rounded ends 232 from digging into expandable member 24 as the garage 206 is retracted relative to expandable member 24.
• Garage 206 is generally cylindrical and is fixed to distal end 57 of separator tube 25.
• Garage 204 preferably has a length at least as long as one of stent segments 32, but preferably less than a combined length of two such stent segments.
• Garage 206 has channels 210 formed to provide a flexible body 212 and permit flexure of the garage during insertion of the catheter toward the treatment region.
• garage 204 is attached to distal portion 54 of separator tube 25 so as to define distal end 57 of separator tube 25.
• garage 204 is designed to have a high radial strength to prevent the expandable member 24 from expanding substantially when the garage is extended over inflatable member 24.
• the garage can be embedded within a distal portion 54 of separator tube 25 (see Figs. 7, 8 and 9 A below).
• Garage 204 can be made from any suitable material, or combination of suitable materials, for example Nickel/Titanium alloy or steel.
• Garage 204, tabs 200 and channels 210 can be formed by laser cutting or lithographic techniques such as photoetching.
• Garage 204 can be formed by mating ends of a photo etched flat plate to form a rounded cylinder.
• garage 204 can be formed from Ni/Ti alloy formed as a round tube which is laser machined.
• engagement member 58 can include a garage 246 within a distal portion 54 of separator tube 25.
• Garage 246 includes a one-way grip structure 248 comprising two axially displaced rows of a repeating pattern of resilient tabs 200, or fingers.
• the tabs can be rectangular shaped to engage prosthetic segments 32.
• a first row of tabs 200 and a second row of tabs 200 are shown but one, three, or more rows could also find use.
• Elongate cutouts 244 are provided in the tabs 200 to decrease and/or set to desired gripping characteristics exerted on segments 32 by tabs 200.
• Anchors 250 are located on garage 246. Anchors 250 secure garage 246 to distal portion 54 of separator tube 25.
• the garage and one-way grip structures as in Fig. 7 can have concave arcuate cutouts 260 on the ends of the rectangular tabs 200 which engage the prosthetic segments. Such cutouts 260 enhance engagement of the tabs 200 with the stent segments 32.
• engagement member 58 which includes a one-way grip structure 300 having an arcuate, resilient flange 302, or finger, in accordance with an embodiment.
• One-way grip structure 300 is located near distal end 57 of separator tube 25.
• One-way grip structure 300 is located within high strength distal portion 54 of the separator tube 25 so that the distal portion of the tube supports the grip structure and prevents expansion of the expandable member as described above.
• One-way grip structure 300 is separated from distal end 57 of the separator tube, and can be separated by any distance as described above.
• One-way grip structure 300 can be used, manufactured and machined similar to the garages described above.

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• Health & Medical Sciences (AREA)
• Engineering & Computer Science (AREA)
• Biomedical Technology (AREA)
• Cardiology (AREA)
• Oral & Maxillofacial Surgery (AREA)
• Transplantation (AREA)
• Heart & Thoracic Surgery (AREA)
• Vascular Medicine (AREA)
• Life Sciences & Earth Sciences (AREA)
• Animal Behavior & Ethology (AREA)
• General Health & Medical Sciences (AREA)
• Public Health (AREA)
• Veterinary Medicine (AREA)
• Media Introduction/Drainage Providing Device (AREA)
• Prostheses (AREA)

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• 2006
  • 2006-01-30 US US11/344,464 patent/US20070179587A1/en not_active Abandoned
• 2007
  • 2007-01-30 AU AU2007211042A patent/AU2007211042A1/en not_active Abandoned
  • 2007-01-30 JP JP2008552623A patent/JP2009525077A/ja active Pending
  • 2007-01-30 CA CA002629392A patent/CA2629392A1/en not_active Abandoned
  • 2007-01-30 WO PCT/US2007/061323 patent/WO2007090128A2/en not_active Ceased
  • 2007-01-30 EP EP07762854A patent/EP1981434A4/en not_active Withdrawn
• 2013
  • 2013-07-19 JP JP2013150197A patent/JP5918175B2/ja active Active

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