US20080255581A1 - Short sleeve stent delivery catheter and methods - Google Patents

Abstract

A stent delivery catheter comprises a catheter body having a proximal end, a distal end, and a guidewire lumen extending from the distal end to at least part way between the proximal end and the distal end. A balloon is disposed over the catheter body near the distal end, and a stent is positioned over the balloon. The stent has a proximal end, a distal end, and a side opening between the proximal end and the distal end. A side sheath is coupled to the catheter body and has a proximal end, a distal end, and a guidewire lumen extending between the proximal end and the distal end. The proximal end of the side sheath is located between the proximal end of the catheter body and the balloon, and the side sheath exits out of the side opening of the stent.

Description

CROSS REFERENCE TO RELATED APPLICATIONS
• This application is a Continuation of U.S. patent application Ser. No. 09/860,744 filed on May 18, 2001, now U.S. Pat. No. 7,387,639, issued on Jun. 17, 2008 entitled SHORT SLEEVE STENT DELIVERY CATHETER AND METHODS, the disclosure of which is incorporated by reference herein in its entirety.
• U.S. Pat. No. 7,387,639 is a continuation-in-part of U.S. patent application Ser. No. 09/325,996, filed Jun. 4, 1999, entitled “CATHETER WITH SIDE SHEATH,” the disclosure of which is herein incorporated by reference. This application claims priority to Ser. No. 09/325,996 to the extent appropriate by law.
• U.S. Pat. No. 7,387,639 also is a continuation-in-part of U.S. patent application Ser. No. 09/455,299, filed Dec. 6, 1999, entitled “CATHETER WITH ATTACHED FLEXIBLE SIDE SHEATH,” the disclosure of which is herein incorporated by reference. This application claims priority to Ser. No. 09/455,299 to the extent appropriate by law.
• U.S. Pat. No. 7,387,639 also is a continuation-in-part of U.S. patent application Ser. No. 09/614,472, filed Jul. 11, 2000, entitled “CATHETER WITH SIDE SHEATH,” which is a continuation-in-part of said Ser. No. 09/325,996, and which is a continuation-in-part of said Ser. No. 09/455,299. The disclosure of said Ser. No. 09/614,472 is herein incorporated by reference. This application claims priority to Ser. No. 09/614,472 to the extent appropriate by law.
• U.S. Pat. No. 7,387,639 also is a continuation-in-part of U.S. patent application Ser. No. 09/663,111, filed Sep. 15, 2000, entitled “CATHETER WITH SIDE SHEATH AND METHODS,” which is a continuation-in-part of said Ser. No. 09/455,299, and which is a continuation-in-part of Ser. No. 09/614,472. The disclosure of said Ser. No. 09/663,111 is herein incorporated by reference. This application claims priority to Ser. No. 09/663,111 to the extent appropriate by law.
BACKGROUND OF THE INVENTION
• This invention relates generally to the field medical catheters, and in some cases, to catheters that are used to deliver medical stents. In one aspect, the invention further relates to techniques for deploying stents into vessels such that a side opening in the stent wall is aligned with an ostium of a branch vessel. In other aspects, the invention is related to the management of guidewires over which such catheters are introduced.
• A type of endoprosthesis device, commonly referred to as a stent, may be placed or implanted within a vein, artery or other tubular body organ for treating occlusions, stenoses, or aneurysms of a vessel by reinforcing the wall of the vessel or by expanding the vessel. Stents have been used to treat dissections in blood vessel walls caused by balloon angioplasty of the coronary arteries as well as peripheral arteries and to improve angioplasty results by preventing elastic recoil and remodeling of the vessel wall. Two randomized multicenter trials have shown a lower restenosis rate in stent treated coronary arteries compared with balloon angioplasty alone (Serruys, P W et al., New England Journal of Medicine 331: 489-495 (1994) and Fischman, D L et al. New England Journal of Medicine 331:496-501 (1994)), the disclosures of which are herein incorporated by reference. Additionally, regular stents have been used at bifurcation lesions with limited success rates (Chevalier, B. et al. American Journal of Cardiology 82:943-949 (1998), Yamashita T. et al. Journal of American College of Cardiology 35:1145-1151 (2000) and Satler S. et al. Catheterization and Cardiovascular Interventions 50:411-412 (2000). Side branch jailing, fear of plaque shifting and total occlusion and difficulty of the procedure require novel, easier to use, special stents to be developed. Stents have been successfully implanted in the urinary tract, the bile duct, the esophagus and the tracheo-bronchial tree to reinforce those body organs, as well as implanted into the neurovascular, peripheral vascular, coronary, cardiac, and renal systems, among others. The term “stent” as used in this Application is a device that is intraluminally implanted within bodily vessels to reinforce collapsing, dissected, partially occluded, weakened, diseased or abnormally dilated or small segments of a vessel wall.
• One of the drawbacks of conventional stents is that they are generally produced in a straight tubular configuration. The use of such stents to treat diseased vessels at or near a bifurcation (branch point) of a vessel may create a risk of compromising the degree of patency of the main vessel and/or its branches, or the bifurcation point and also limits the ability to insert a branch stent into the side branch if the result of treatment of the main, or branch vessel is suboptimal. Suboptimal results may occur as a result of several mechanisms, such as displacing diseased tissue, plaque shifting, snow plowing, chronic total occlusion, vessel spasm, dissection with or without intimal flaps, thrombosis, and embolism.
• As described in related co-pending U.S. patent application Ser. No. 08/744022 filed Nov. 4, 1996 (now abandoned); Ser. No. 09/007265 filed Jan. 14, 1998; Ser. No. 08/935,383 filed Sep. 23, 1997; No. 60/088301 filed Jun. 5, 1998; Ser. No. 09/663,111, filed Sep. 15, 2000, and Ser. No. 09/794,740, filed Feb. 26, 2001; and PCT Patent Application Publication No. WO 99/00835 filed Jan. 14, 1998; systems and methods have been developed for deploying a main stent in a main vessel at the intersection of a main vessel and a branch vessel. Further, a branch stent may optionally be positioned within a branch vessel through a side opening in the main stent. The complete disclosures of all these references are herein incorporated by reference.
• When using multiple guidewires to introduce a catheter system through body lumens, one condition that may occur is known as “wire crossing”. In such cases, the guidewires over which the catheter system is advanced intertwine within the guide catheter and vasculature. This condition may prevent the successful delivery of the catheter system by impeding its travel and, subsequently, the alignment of the stent's side opening with the ostium of the branch vessel.
• This invention relates to other novel techniques and delivery systems for deploying stents at vessel intersections to permit the side opening to be aligned with the ostium of the branch vessel, among other features. Some embodiments are particularly directed toward managing the guidewires used to introduce the catheter systems to the region of interest. Some embodiments are also directed toward facilitating easy introduction and removal of catheter systems.
SUMMARY OF THE INVENTION
• In one embodiment, the invention provides an exemplary stent delivery catheter that may be employed to deliver a stent to a particular region of interest within a patient's vasculature. In some cases, the delivery catheter may not include a stent and may be used in other procedures, such as conventional balloon angioplasty.
• The catheter comprises a catheter body having a proximal end, a distal end, and a guidewire lumen extending from the distal end to at least part way between the proximal end and the distal end. For example, the guidewire lumen may extend fully to the proximal end, or may terminate in a side opening anywhere proximal to an accompanying stent to provide the catheter with side or short exchange capabilities. In one aspect, the side opening may be within about 1 cm to about 150 cm of the distal end. A balloon is disposed over the catheter body near the distal end, and in some embodiments a stent positioned over the balloon. The stent in one embodiment has a proximal end, a distal end, and a side opening between the proximal end and the distal end. A side sheath is coupled to the catheter body and has a proximal end, a distal end, and a guidewire lumen extending between the proximal end and the distal end. The proximal end of the side sheath is located at some point proximal to the balloon. In one aspect, the side sheath may pass through the proximal end of the stent and exit out of the side opening.
• The use of the shortened side sheath provides a number of significant advantages. For example, shorter guidewires may be used to introduce the catheter. For example, guidewires ranging from about 100 cm to about 200 cm, and more preferably about 150 cm, may be used instead of conventional 300 cm guidewires. In this way, the catheter may be introduced and withdrawn from the patient by a single worker. Another significant feature is that the overall profile of the catheter is reduced to allow the catheter to be introduced into smaller guide catheters, thereby reducing trauma to the patient. For example, the catheter profile may be as low as about 4 to 7 French. The smaller profile also permits the catheter to be more easily maneuvered and rotated during introduction to the patient. For example, the reduction is profile permits the catheter to be introduced adjacent to a backup guidewire in the main vessel. If any wire crossing occurs between the back up guidewire and the branch vessel guidewire, the catheter may more easily be torqued by the physician to overcome the wire crossing.
• In one aspect, the side sheath extends out of the side opening by a distance of at least about 0 cm to about 7 cm, and the catheter body has a length in the range from about 50 cm to about 150 cm. In another aspect, the catheter body further includes a balloon inflation lumen that is in fluid communication with the balloon. For example, the balloon inflation lumen may be coaxially disposed about the guidewire lumen. Conveniently, a hub may be coupled to the distal end to facilitate balloon inflation and guidewire introduction.
• In a further aspect, the catheter body includes at least one radiopaque marker near the balloon, and the side sheath includes at least one radiopaque marker near the distal end. In this way, separation of the markers may be observed to indicate that the side sheath has advanced into the branch vessel.
• In one particular embodiment, the catheter body guidewire lumen terminates at the proximal end. Alternatively, the catheter body guidewire lumen may terminate in a side port within the catheter body at a location anywhere proximal to the balloon. For example, the side port may be located within about 1 cm to about 150 cm of the distal end. In this way, the overall profile of the catheter may be further reduced, with both the branch vessel guidewire and the main vessel guidewire may extend along the outside of the catheter body. Such a configuration further provides short or side exchange capabilities for the catheter. Reduction in profile size may be accomplished, for example, by constructing the catheter body from a tubular member, such as a hypo tube, surrounded by a nylon jacket. A stiffening mandrel may also be incorporated into a distal portion of the catheter body to provide torquing capabilities.
• In embodiments where no stent is used, a second balloon may be provided on side sheath. In this way, the catheter may be used in “kissing the balloon” procedures where the balloons are simultaneously inflated into two separate vessels.
• The invention further provides an exemplary method for placing a stent having a side hole into a main vessel such that the side hole is aligned with an ostium of a branch vessel that extends from the main vessel. Conveniently, the method may utilize a catheter similar to the catheter previously described. When using such a catheter, a branch vessel guidewire is introduced into the main vessel until a distal end of the branch vessel guidewire passes into the branch vessel, and a primary main vessel guidewire is introduced through the catheter body guidewire lumen. The catheter containing the primary main vessel guidewire is introduced over the branch vessel guidewire such that the branch vessel guidewire passes through the side sheath. The catheter is advanced over the branch vessel guidewire until the side sheath is within the branch vessel and the side opening of the stent is aligned with an ostium of the branch vessel. At this point, the balloon may be inflated to deploy the stent.
• By advancing the catheter over a single guidewire, i.e., the branch vessel guidewire, the problem of wire crossing is significantly reduced. After the side sheath is near or into the branch vessel, the primary main guidewire may be further advanced into the main vessel.
• In some cases, a physician will not want to lose wire placement and will therefore desired to maintain a guidewire within the main vessel at all times. In such cases, a secondary or back up main vessel guidewire may be inserted into the main vessel such that a distal end of the secondary main vessel guidewire passes beyond the ostium of the branch vessel prior to inserting the catheter over the branch vessel guidewire. Once the catheter is near the ostium and the primary main vessel guidewire has been advanced through the catheter, the secondary main vessel guidewire may be withdrawn prior to inflation of the balloon. If the branch vessel guidewire and the secondary main vessel guidewire cross, the catheter body may be torqued during insertion in order to overcome the wire crossing. The wire crossing may be overcome since the secondary main vessel guidewire runs along side of the catheter. Since the profile of the catheter may be relatively small, maneuvering of the catheter within the patient is also facilitated.
• After withdrawing the secondary main vessel guidewire, the catheter may be further advanced over the branch vessel guidewire and the primary main vessel guidewire to align the side opening in the stent with the ostium. After the stent has been deployed, the balloon may be deflated, and the catheter may be withdrawn from the main vessel and the branch vessel. Conveniently, the catheter body may include at least one marker and the side sheath may also include at least one marker. With this configuration, separation of the markers may be observed fluoroscopically to indicate that the catheter body has passed beyond the ostium and the side member extends into the branch vessel. In one aspect, the primary main vessel guidewire distally extends typically about1 cm to about3 cm from the catheter body while the catheter is being advanced over the branch vessel guidewire. In another aspect, the catheter is advanced over the branch vessel guidewire until the balloon exits a guiding catheter. At that point, the primary main vessel guidewire may be extended further into the main vessel.
• In one particular aspect, the catheter body guidewire lumen terminates in a side port within the catheter body at a location within about 1 cm to about 150 cm of the distal end. With such a configuration, the primary main vessel guidewire is routed through the guidewire lumen in the catheter body until exiting through the side port.
• The catheters described above may be introduced to the region of interest using other techniques as well. For example, both the branch vessel guidewire and the main vessel guidewire may initially be placed into the branch and main vessels, respectively. The catheter may then be routed over both guidewires. As another example, the branch and main vessel guidewires may both be preloaded into the catheter. The preloaded catheter may then be advanced through the main vessel until exiting the guiding catheter. At this point, the branch vessel guidewire may be advanced through the side sheath and into the branch vessel, and the main vessel guidewire may be advanced through the catheter body and further into the main vessel. With the guidewires in place, the catheter may be advanced into position in a manner similar to that previously described.
BRIEF DESCRIPTION OF THE DRAWINGS
• FIG. 1 is a side view of one embodiment of a delivery catheter according to the invention.
• FIG. 2 is a cross sectional enlarged view of a section2 of the catheter ofFIG. 1.
• FIG. 3 is a cross sectional enlarged view of a section3-3 of the catheter ofFIG. 2.
• FIG. 4 illustrates a distal portion of the catheter ofFIG. 2 when introduced to a bifurcated vessel using a three guidewire technique according to the invention.
• FIGS. 5 through 9 schematically illustrate a technique for deploying a stent using the catheter ofFIG. 1.
• FIGS. 10 through 12 schematically illustrate another technique for deploying a stent using the catheter ofFIG. 1.
• FIGS. 13 through 16 schematically illustrate still another technique for deploying a stent using the catheter ofFIG. 1.
• FIG. 17 is a side view of another embodiment of a delivery catheter according to the invention.
• FIG. 18 is a cross sectional enlarged view of asection18 of the catheter ofFIG. 17.
• FIG. 19 is a cross sectional view of the catheter ofFIG. 17 taken along lines19-19.
DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENT
• In one aspect, the invention provides systems and methods for deploying stents at a vessel bifurcation such that a cell in the stent that is specifically designed to function as a branch aperture (referred to herein as a side hole of the stent) is in registry with the ostium of the branch vessel. Further, various techniques are provided for managing the guidewires over which the stents and stent delivery catheters are directed. More specifically, the invention provides techniques to help prevent the crossing of guidewires or to traverse crossed guidewires when introducing catheters used to deploy stents or other devices that require advancement over multiple guidewires, where it is important for the guidewires to be tangle free and parallel with respect to each other. In this way, the catheters may more easily be introduced to the diseased region.
• The invention also provides techniques for reducing the profile of such delivery catheters, and to facilitate the introduction, withdrawal and exchange of such catheters. In one aspect, the invention provides catheters that may be used with shorter guidewires so that they are useful with short or side exchange techniques.
• Applications of the invention include the cardiac, coronary, renal, peripheral vascular, gastrointestinal, pulmonary, urinary and neurovascular systems and the brain.
• Advantages of the invention include, but are not limited to, the use of an improved stent delivery apparatus, which may deliver stents to: 1) completely cover the bifurcation point of bifurcation vessels; 2) be used to treat lesions in one branch of a bifurcation while preserving access to the other branch for future treatment; 3) allow for differential sizing of the stents in a bifurcated stent apparatus even after a main stent is implanted; 4) treat bifurcation lesions in a bifurcated vessel where the branch vessel extends from the side of the main vessel; and 5) be marked with, or at least partly constructed of, material which is imageable by commonly used intraluminal catheterization visualization techniques including but not limited to ultrasound or x-ray.
• Some catheters and techniques of the invention may be used with non-stent applications. For example, the introduction techniques may be used with a wide variety of catheter designs that may be used to simultaneously inflate two balloons (to prevent a “snowplowing” effect), to prevent injury during introduction, and the like.
• As described herein, a side hole in the main vessel stent refers to specific cell of the stent, which form a relatively large opening and which is intended to be aligned with the ostium of the branch vessel. Such a side hole is separate from any of the multiple passageways extending through the side of the stent between struts in the stent geometry. Accordingly, the side hole in the stent is a hole, which is understood to be larger than other passages through the stent, except the longitudinal bore of the stent itself. Additionally the side hole of the stent is configured such that a central axis extending perpendicularly through the side hole is generally perpendicular to the longitudinal axis of the stent. In some aspects, this side hole is defined by a band of continuous material, which outlines the perimeter of the side hole. This continuous band of material preferably comprises serpentine patterns over its length so that the area of the side hole expands together with the expansion of the stent. In various aspects, the continuous band comprises protrusions, which project inwardly from a peripheral edge of the side opening and, when expanded, deflect perpendicularly to the longitudinal axis of the stent. Preferably, these protrusions (or expandable portions) are initially aligned within a cylindrical envelope of the tubular body of the stent.
• In one embodiment, the invention provides an elongate catheter body having a lumen through which a guidewire may be inserted. The guidewire lumen begins at a distal end and may terminate at the proximal end or somewhere between the proximal end and the distal end. A shorter catheter body is attached to or integrally formed with the longer catheter body. The shorter catheter body also includes a guidewire lumen. The two catheter bodies separate at their distal ends, and one of the catheter bodies includes a balloon near the distal end and a balloon inflation lumen is provided to inflate the balloon. In this way, a stent with a side opening may be crimped over the balloon, with the distal end of the other catheter body passing between the stent and the balloon, and exiting out of the side opening. The shorter catheter body preferably terminates within about 1 cm to about 150 cm of the balloon.
• The use of the shorter catheter body permits the catheter to be used with shorter guidewires. For example, guidewires ranging from about 100 cm to about 200 cm, and more preferably about 150 cm, may be used instead of conventional 300 cm guidewires. In this way, the catheter may be introduced and withdrawn from the patient by a single worker because the shorter catheter body proximally extends only a short distance over the guidewire after initial loading. Another significant feature is that the overall profile of the catheter is reduced to allow the catheter to be introduced into smaller guide catheters, thereby reducing trauma to the patient. For example, the catheter profile may be as low as about 4 to 7 French. The smaller profile also permits the catheter to be more easily maneuvered and rotated during introduction to the patient. In this way, the side opening may easily be radially aligned with the ostium of the branch vessel because the catheter may turn itself into radial alignment during insertion. As another example, if the catheter is inserted next to a back up guidewire in the main vessel, the catheter may more easily be torqued by the physician to overcome any wire crossing with the back up guide wire. Such a catheter may conveniently be advanced over a single guidewire, or over a pair of guidewires.
• The invention further provides an exemplary technique for introducing a catheter having two guidewire lumens to a vessel bifurcation. Although well suited for catheters having a shortened catheter body relative to the other catheter body, it will be appreciated that the techniques may be used with any catheter having two guidewire lumens for receiving parallel guidewires. The technique preloads one of the guidewires that is to remain within the main vessel into one of the guidewire lumens. The distal end of this guidewire may extend typically about 1 cm to about 3 cm beyond the distal end of the catheter body. The other guidewire is inserted into the main vessel until a distal end extends into the branch vessel. The preloaded catheter is then inserted over the branch vessel guidewire and advanced through the main vessel. When the catheter body is near the vessel bifurcation, the preloaded guidewire is advanced out of the catheter body and further into the main vessel beyond the vessel bifurcation. The catheter may then be advanced over both guidewires until the one of the catheter bodies is within the branch vessel. If desired, a backup main vessel guidewire may be positioned within the main vessel prior to introduction of the catheter. When using three guidewires, any of the techniques described in copending U.S. application Ser. No. 09/794,740, filed Feb. 26, 2001, previously incorporated by reference, may also be used.
• Referring now toFIG. 1, one embodiment of adelivery catheter10 will be described.Catheter10 comprises acatheter body12 having aproximal end14 and adistal end16. As best shown inFIG. 2, aguidewire lumen20 extends betweenproximal end14 anddistal end16.Catheter body12 functions as a main shaft and is constructed of a relatively stiff material, such as a polyamide, PEEK, stainless steel hypotubes or the like to provide torquability to the catheter body.Proximal end14 is coupled to an inflation/deflation hub22 having astrain relief portion24.Hub22 further includes aguidewire exit port26 which leads toguidewire lumen20, and aballoon inflation port28. At a bond joint29, a length ofdual lumen tubing31 is coupled. As best shown inFIG. 3, one of these lumens is a coaxial lumen and includes aballoon inflation lumen30 that is coaxially disposed aboutguidewire lumen20.Balloon inflation port28 is in fluid communication withballoon inflation lumen30.
• Disposed about a distal portion ofcatheter body12 is aballoon32 that is in fluid communication withballoon inflation lumen30. In this way,balloon32 may be inflated and deflated fromport28 as is known in the art. Loaded ontoballoon32 is astent34 having aproximal end36, adistal end38 and aside opening40.Stent34 is radially expanded during inflation ofballoon32 in order to deploystent34 within a vessel.
• Coupled tocatheter body12 is aside sheath42 that has a proximal end that terminates in anexit port44 and adistal end46. Aguidewire lumen48 extends betweenexit port44 anddistal end46. As shown best inFIG. 2,side sheath42 passes throughproximal end36 and exits out ofside opening40.Distal end46 may extend about 0.1 cm to about 7 cm out ofside opening40 to facilitate entry ofside sheath42 into a branch vessel.
• Side sheath42 is attached tocatheter body12 at some point proximal toballoon32 so that the rest ofside sheath42 is unattached and free to be manipulated.Side sheath42 may be integrally formed withcatheter body12 where attached, or may be separated secured, such as with a bonding material, with a sleeve, or the like.Exit port44 is preferably within about 1 cm to about 150 cm ofballoon32, more preferably within about 1 cm to about 15 cm, and most preferably within about 1 cm to about 5 cm. With such a configuration, a branch vessel guidewire that is used facilitate alignment ofside opening40 with an ostium of a branch vessel may extend alongside catheter body12. In this way, the overall size ofcatheter12 may be reduced. Further, such a configuration may be used to improve guidewire management, such as when loading the catheter with guidewires, when manipulating the catheter to overcome a wire crossing, when using three guidewire introduction techniques, and the like. Another advantage of such a design is the simplification ofhub22 that only includes two ports. Such a part may more easily be injection molded and requires leak testing for only two ports.
• Referring also now toFIG. 4, a distal portion ofcatheter10 is shown at the location of a vessel bifurcation. A main vessel guidewire50 extends throughguidewire lumen20 and into the main vessel beyond the bifurcation. A branch vessel guidewire52 extends throughguidewire lumen48 and into the branch vessel. Because of the reduced profile, abackup guidewire54 may also be positioned in the main vessel alongside ofcatheter10 and will be described in greater detail hereinafter.
• As best shown inFIG. 2,catheter body12 includes a set ofradiopaque markers56, andside sheath42 also includes aradiopaque marker58.Markers56 and58 may be used to facilitate angiographic visualization ofcatheter10 to insure proper placement ofstent34. For example, when in the position shown inFIG. 4,marker58 separates relative tomarkers56 to indicate thatside sheath42 has successfully reached the branch vessel, thereby aligningside opening40 with the ostium of the branch vessel.
• Referring now toFIGS. 5-9, one method for deliveringstent34 usingcatheter10 will be described schematically. Initially, aguide catheter56 is introduced to extend past the aortic arch as in known in the art. A backup main vessel guidewire58 is inserted throughcatheter56 and beyond the vessel bifurcation as shown inFIG. 5. Branch vessel guidewire52 is also inserted throughcatheter56 and into the branch vessel.
• As shown inFIG. 6, main vessel guidewire50 is introduced throughcatheter body12 until extending about1 to3 cm beyondcatheter body12 to preloadcatheter10. When preloaded, branch vessel guidewire52 is routed throughside sheath42 and then advanced throughguide catheter56 overguidewire52. Conveniently, this may be done using short or side exchange techniques and shorter guidewires sinceguidewire52 may be grasped by the caregiver as soon as it exitsport44. Once exitingguide catheter56, guidewire50 is advanced out ofcatheter body12 and further into the main vessel as shown inFIG. 7. Thebackup guidewire58 is then withdrawn as shown inFIG. 8.
• Catheter10 is then advanced over bothguidewires50 and52 under fluoroscopic visualization untilside sheath42 is within the branch vessel andside opening40 is aligned with the ostium.Balloon32 is then inflated to deploystent34, withside opening40 being aligned with the ostium as shown inFIG. 9.Balloon32 may then be deflated andcatheter10 removed from the patient.
• By preloadingcatheter10 ontoguidewire50,catheter10 may be inserted over a single guidewire, i.e., guidewire52. In this way, no guidewire crossing occurs betweenguidewires50 and52. Further, ifguidewires52 and58 cross,catheter10 may be torqued and manipulated to forcecatheter10 past the wire crossing. This is possible becauseguidewire58 is exterior tocatheter10.
• Although shown withbackup guidewire58, it will be appreciated that the method ofFIGS. 5 through 9 may be performed withoutbackup guidewire58. In this way, essentially no wire crossing will occur.
• Shown inFIGS. 10 through 12 is an alternative method for deployingstent34 usingcatheter10. As shown inFIG. 10, main vessel guidewire50 is inserted throughcatheter56 and past the branch vessel. Branch vessel guidewire52 is also inserted throughcatheter56 and into the branch vessel.Catheter10 is then loaded ontoguidewires50 and52 while outside the patient, withguidewire50 passing throughcatheter body12 and guidewire52 passing throughside sheath42.Catheter10 is advanced overguidewires50 and52 under angiographic imaging until side opening40 ofstent34 is aligned with the branch vessel as shown inFIGS. 11 and 12.Balloon32 may then be inflated to deploystent34. Afterdeployment balloon32 is deflated andcatheter10 is removed from the patient.
• FIGS. 13 through 16 illustrate still another method for deployingstent34 usingcatheter10. As shown inFIG. 13,catheter10 is preloaded ontoguidewires50 and52, withguidewire50 extending throughcatheter body12 and guidewire52 extending throughside sheath42.Guidewires50 and52 may extend about 1 to about 3 cm.Preloaded catheter10 is then introduced through guide catheter56 (which was previously inserted) and shown inFIG. 14. When the distal ends ofguidewires50 and52 reach or are near to the vessel bifurcation (which corresponds to the mouth of guide catheter56), guidewires50 and52 are extended fromcatheter10 untilguidewire10 is further within the main vessel and guidewire52 is within the branch vessel as shown inFIG. 15.Catheter10 is advanced overguidewires50 and52 under angiographic imaging until side opening40 ofstent34 is aligned with the branch vessel as shown inFIG. 16.Balloon32 may then be inflated to deploystent34. Afterdeployment balloon32 is deflated andcatheter10 is removed from the patient.
• FIGS. 17 through 19 show another embodiment of astent delivery catheter100 that is constructed such that both the main vessel guidewire and the branch vessel guidewire is routed only partially through the catheter to provide a smaller design, to provide dual short or side exchange capabilities and to permit the use of shorter guidewires, as well as other features previously described in connection withcatheter10.Catheter100 comprises acatheter body112 having aproximal end114 and adistal end116.Catheter body112 may conveniently be divided into aproximal portion120 and adistal portion122.Proximal portion120 may be constructed of ahypo tube123 and be connected to an inflation/deflation hub124 having astrain relief portion126.Proximal portion120 is coupled todistal portion122 at ajoint bond126.
• As best shown inFIG. 19,distal portion122 comprises a length of dual lumen tubing having aballoon inflation lumen128 that is coaxially disposed about aguidewire lumen130. Also included is a sidesheath guidewire lumen132. Disposed withinlumen128 is atapered stiffening mandrel134 to provide rigidity and torquability todistal portion122.Mandrel134 is connected toproximal portion120 at aweld point136.
• As best shown inFIGS. 17 and 18, the dual length tubing ofdistal portion122 separates into two separate lengths of tubing, one of which is conveniently identified as a continuation ofcatheter body112, and the other being identified as aside sheath138 which includeslumen132. Coupled tocatheter body112 neardistal end116 is aballoon140 that is in fluid communication withballoon inflation lumen122 to permitballoon140 to be inflated and deflated fromhub124.Guidewire lumen130 continues todistal end116 and proximally terminates at aside opening142 that may be located anywhere betweenhub124 andballoon140. In this way, the profile ofcatheter100 may be reduced, andside port142 provides short or side exchange capabilities for the guidewire extending throughlumen130.
• Disposed overballoon140 is astent144 having aside opening146.Side sheath138 exitsside opening146 in a manner similar to that described with previously embodiments. Also similar to previous embodiments,side sheath138 proximally terminates in aside port148 somewhere betweenhub124 andballoon140. In this way,catheter100 is provided with short or side exchange capabilities for the branch vessel guidewire that extends throughside sheath138 as well as for the main vessel guidewire passing throughlumen130.
• In use,catheter100 may be introduced using any of the techniques previously described in order to deploystent144. To facilitate alignment ofside opening146, fluoroscopicallyvisible markers150 and152 may be included. These markers separate asside sheath138 passes into the branch vessel as previously described.
• Catheter100 has the additional feature of side or short exchange guidewire capabilities usingside port142. Sinceside sheath138 also has a side exit port, dual short guidewire exchange capabilities are provided. Further, by running both guidewire along side of the catheter, the overall profile may be further reduced to enhance the benefits previously described.
• The invention has now been described in detail for purposes of clarity and understanding. However, it will be appreciated that certain changes and modifications may be made within the scope of the appended claims.
• The above specification, examples and data provide a complete description of the manufacture and use of the composition of the invention. Since many embodiments of the invention can be made without departing from the spirit and scope of the invention, the invention resides in the claims hereinafter appended.

Claims (8)

1. A method for placing a stent having a side hole into a main vessel such that the side hole is aligned with an ostium of a branch vessel that extends from the main vessel, the method comprising:

(a) providing a delivery catheter that comprises a catheter body having a proximal end, a distal end, and a guidewire lumen extending from the distal end to at least part way between the proximal end and the distal end;

i. a balloon disposed over the catheter body near the distal end; a stent positioned over the balloon, the stent having a proximal end, a distal end, and a side opening between the proximal end and the distal end; and

ii. a side sheath coupled to the catheter body, the side sheath having a proximal end, a distal end, and a guidewire lumen extending between the proximal end and the distal end, wherein the proximal end of the side sheath is located between the proximal end of the catheter body and the balloon, and wherein the side sheath exits out of the side opening of the stent;

(b) introducing a main vessel guidewire into the main vessel until a distal end of the main vessel guidewire passes beyond the branch vessel;

(c) introducing a branch vessel guidewire into the main vessel until a distal end of the branch vessel guidewire passes into the branch vessel;

(d) inserting the catheter over the branch vessel guidewire and the main vessel guidewire such that the main vessel guidewire passes through the guidewire lumen of the catheter body and the branch vessel guidewire passes through the side sheath;

(e) advancing the catheter over the main vessel guidewire and the branch vessel guidewire until the side sheath is within the branch vessel and the side opening of the stent is aligned with an ostium of the branch vessel; and

(f) inflating the balloon to deploy the stent.

2. A method as inclaim 1, further comprising deflating the balloon and withdrawing the catheter from the main vessel and the branch vessel.

3. A method as inclaim 1, wherein the catheter body includes at least one marker and the side sheath includes at least one marker, and further comprising observing separation of the markers to indicate that the catheter body has passed beyond the ostium and the side member extends into the branch vessel using angiographic imaging.

4. A method as inclaim 1, wherein the catheter body guidewire lumen terminates in a side port within the catheter body at a location within about 1 cm to about 150 cm of the distal end, and further comprising routing the main vessel guidewire through the guidewire lumen in the catheter body until exiting through the side port.

5. A method for placing a stent at a vessel bifurcation using a delivery catheter, the delivery catheter including a catheter body, a balloon, a stent, and a side sheath, the catheter body having a proximal end, a distal end, and a guidewire lumen, the balloon being disposed over the catheter body near the distal end, the stent being positioned over the balloon, the stent having a proximal end, a distal end, and a side opening between the proximal end and the distal end, the side sheath being coupled to the catheter body, the side sheath having a proximal end, a distal end, and a guidewire lumen extending between the proximal end and the distal end, wherein the proximal end of the side sheath is located between the proximal end of the catheter body and the balloon, and wherein the side sheath exits out of the side opening of the stent, the method comprising:

(a) introducing a main vessel guidewire into the main vessel until a distal end of the main vessel guidewire passes beyond the branch vessel;

(b) introducing a branch vessel guidewire into the main vessel until a distal end of the branch vessel guidewire passes into the branch vessel;

(c) advancing the catheter over the main vessel guidewire and the branch vessel guidewire until the side sheath is within the branch vessel and the side opening of the stent is aligned with an ostium of the branch vessel; and

(d) inflating the balloon to deploy the stent.

6. A method as inclaim 5, further comprising deflating the balloon and withdrawing the catheter from the main vessel and the branch vessel.

7. A method as inclaim 5, wherein the catheter body includes at least one marker and the side sheath includes at least one marker, and further comprising observing separation of the markers to indicate that the catheter body has passed beyond the ostium and the side member extends into the branch vessel.

8. A method as inclaim 5, wherein the catheter body guidewire lumen terminates in a side port within the catheter body at a location within about 1 cm to about 150 cm of the distal end, and further comprising routing the main vessel guidewire through the guidewire lumen in the catheter body until exiting through the side port.

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