US20010044598A1 - Apparatus and methods for reducing embolization during treatment of carotid artery disease - Google Patents

Abstract

Methods and apparatus are provided for removing emboli during an angioplasty, stenting or surgical procedure comprising a catheter having an occlusion element, an aspiration lumen, and a blood outlet port in communication with the lumen, a guide wire having a balloon, a venous return catheter with a blood inlet port, and tubing that couples the blood outlet port to the blood inlet port. Apparatus is also provided for occluding the external carotid artery to prevent reversal of flow into the internal carotid artery. The pressure differential between the artery and the vein provides reverse flow through the artery, thereby flushing emboli. A blood filter may optionally be included in-line with the tubing to filter emboli from blood reperfused into the patient.

Description

REFERENCE TO RELATED APPLICATIONS
• The present application is a continuation-in-part of U.S. patent application Ser. No. 09/333,074, filed Jun. 14, 1999, which is a continuation-in-part of International Application PCT/US99/05469, filed Mar. 12, 1999, which is a continuation-in-part of U.S. patent application Ser. No. 09/078,263, filed Mar. 5, 1998.[0001]
FIELD OF THE INVENTION
• This invention relates to apparatus and methods for protecting against embolization during vascular interventions, such as carotid artery angioplasty and endarterectomy. More particularly, the apparatus and methods of the present invention induce substantially continuous retrograde flow through the internal carotid artery during treatment during an interventional procedure, without significant blood loss.[0002]
BACKGROUND OF THE INVENTION
• Carotid artery stenoses typically manifest in the common carotid artery, internal carotid artery or external carotid artery as a pathologic narrowing of the vascular wall, for example, caused by the deposition of plaque, that inhibits normal blood flow. Endarterectomy, an open surgical procedure, traditionally has been used to treat such stenosis of the carotid artery.[0003]
• An important problem encountered in carotid artery surgery is that emboli may be formed during the course of the procedure, and these emboli can rapidly pass into the cerebral vasculature and cause ischemic stroke.[0004]
• In view of the trauma and long recuperation times generally associated with open surgical procedures, considerable interest has arisen in the endovascular treatment of carotid artery stenosis. In particular, widespread interest has arisen in transforming interventional techniques developed for treating coronary artery disease, such as angioplasty and stenting, for use in the carotid arteries. Such endovascular treatments, however, are especially prone to the formation of emboli.[0005]
• Such emboli may be created, for example, when an interventional instrument, such as a guide wire or angioplasty balloon, is forcefully passed into or through the stenosis, as well as after dilatation and deflation of the angioplasty balloon or stent deployment. Because such instruments are advanced into the carotid artery in the same direction as blood flow, emboli generated by operation of the instruments are carried directly into the brain by antegrade blood flow.[0006]
• Stroke rates after carotid artery stenting have widely varied in different clinical series, from as low as 4.4% to as high as 30%. One review of carotid artery stenting including data from twenty-four major interventional centers in Europe, North America, South America and Asia, had a combined initial failure and combined mortality/stroke rate of more than 7%. Cognitive studies and reports of intellectual changes after carotid artery stenting indicate that embolization is a common event causing subclinical cerebral damage.[0007]
• Several previously known apparatus and methods attempt to remove emboli formed during endovascular procedures by trapping or suctioning the emboli out of the vessel of interest. These previously known systems, however, provide less than optimal solutions to the problems of effectively removing emboli.[0008]
• Solano et al. U.S. Pat. No. 4,921,478 describes cerebral angioplasty methods and devices wherein two concentric shafts are coupled at a distal end to a distally-facing funnel-shaped balloon. A lumen of the innermost shaft communicates with an opening in the funnel-shaped balloon at the distal end, and is open to atmospheric pressure at the proximal end. In use, the funnel-shaped balloon is deployed proximally (in the direction of flow) of a stenosis, occluding antegrade flow. An angioplasty balloon catheter is passed through the innermost lumen and into the stenosis, and then inflated to dilate the stenosis. The patent states that when the angioplasty balloon is deflated, a pressure differential between atmospheric pressure and the blood distal to the angioplasty balloon causes a reversal of flow in the vessel that flushes any emboli created by the angioplasty balloon through the lumen of the innermost catheter.[0009]
• While a seemingly elegant solution to the problem of emboli removal, several drawbacks of the device and methods described in the Solano et al. patent seem to have lead to abandonment of that approach. Chief among these problems is the inability of that system to generate flow reversal during placement of the guide wire and the angioplasty balloon across the stenosis. Because flow reversal does not occur until after deflation of the angioplasty balloon, there is a substantial risk that any emboli created during placement of the angioplasty balloon will travel too far downstream to be captured by the subsequent flow reversal. It is expected that this problem is further compounded because only a relatively small volume of blood is removed by the pressure differential induced after deflation of the angioplasty balloon.[0010]
• Applicant has determined another drawback of the method described in the Solano patent: deployment of the funnel-shaped balloon in the common carotid artery (“CCA”) causes reversal of flow from the external carotid artery (“ECA”) into the internal carotid artery (“ICA”), due to the lower flow impedance of the ICA. Consequently, when a guide wire or interventional instrument is passed across a lesion in either the ECA or ICA, emboli dislodged from the stenosis are introduced into the blood flow and carried into the cerebral vasculature via the ICA.[0011]
• The insufficient flow drawback identified for the system of the Solano patent is believed to have prevented development of a commercial embodiment of the similar system described in EP Publication No. 0 427 429. EP Publication No. 0 427 429 describes use of a separate balloon to occlude the ECA prior to crossing the lesion in the ICA. However, like Solano, that publication discloses that flow reversal occurs only when the dilatation balloon in the ICA is deflated.[0012]
• [0013]Chapter46 ofInterventional Neuroradioloy: strategies and practical techniques(J. J. Connors & J. Wojak, 1999), published by Saunders of Philadelphia, Pa., describes using a coaxial balloon angioplasty system for patients having with proximal ICA stenoses. In particular, a small, deflated occlusion balloon on a wire is introduced into the origin of the ECA, and a guide catheter with a deflated occlusion balloon is positioned in the CCA just proximal to the origin of the ECA. A dilation catheter is advanced through a lumen of the guide catheter and dilated to disrupt the stenosis Before deflation of the dilation catheter, the occlusion balloons on the guide catheter and in the ECA are inflated to block antegrade blood flow to the brain. The dilation balloon then is deflated, the dilation catheter is removed, and blood is aspirated from the ICA to remove emboli.
• Applicant has determined that cerebral damage still may result from the foregoing previously known procedure, which is similar to that described in EP Publication No. 0 427 429, except that the ICA is occluded prior to the ECA. Consequently, both of these previously known systems and methods suffer from the same drawback—the inability to generate flow reversal at sufficiently high volumes during placement of the guide wire and dilation catheter across the stenosis. Both methods entail a substantial risk that any emboli created during placement of the balloon will travel too far downstream to be captured by the flow reversal.[0014]
• Applicants note, irrespective of the method of aspiration employed with the method described in the foregoing[0015]Interventional Neuroradiologyarticle, substantial drawbacks are attendant. If, for example, natural aspiration is used (i.e., induced by the pressure gradient between the atmosphere and the artery), then only a relatively small volume of blood is expected to be removed by the pressure differential induced after deflation of the angioplasty balloon. If, on the other hand, an external pump is utilized, retrieval of these downstream emboli may require a flow rate that cannot be sustained for more than a few seconds, resulting insufficient removal of emboli.
• Furthermore, with the dilation balloon in position, the occlusion balloons are not inflated until after inflation of the dilation balloon. Microemboli generated during advancement of the dilation catheter into the stenosed segment may therefore be carried by retrograde blood flow into the brain before dilation, occlusion, and aspiration are even attempted.[0016]
• A still further drawback of both the device in EP Publication No. 0 427 429 and the[0017]Interventional Neuroradiologydevice is that, if they are used for placing a stent in the ICA instead of for ICA angioplasty, the stent often extends beyond the bifurcation between the ECA and the ICA. The occlusion balloon placed by guide wire in the ECA may snag the stent during retrieval. Emergency surgery may then be required to remove the balloon.
• Imran U.S. Pat. No. 5,833,650 describes a system for treating stenoses that comprises three concentric shafts. The outermost shaft includes a proximal balloon at its distal end that is deployed proximal of a stenosis to occlude antegrade blood flow. A suction pump then draws suction through a lumen in the outermost shaft to cause a reversal of flow in the vessel while the innermost shaft is passed across the stenosis. Once located distal to the stenosis, a distal balloon on the innermost shaft is deployed to occlude flow distal to the stenosis. Autologous blood taken from a femoral artery using an extracorporeal blood pump is infused through a central lumen of the innermost catheter to provide continued antegrade blood flow distal to the distal balloon. The third concentric shaft, which includes an angioplasty balloon, is then advanced through the annulus between the innermost and outermost catheters to dilate the stenosis.[0018]
• Like the device of the Solano patent, the device of the Imran patent appears to suffer the drawback of potentially dislodging emboli that are carried into the cerebral vasculature. In particular, once the distal balloon of Imran's innermost shaft is deployed, flow reversal in the vasculature distal to the distal balloon ceases, and the blood perfused through the central lumen of the innermost shaft establishes antegrade flow. Importantly, if emboli are generated during deployment of the distal balloon, those emboli will be carried by the perfused blood directly into the cerebral vasculature, and again pose a risk of ischemic stroke. Moreover, there is some evidence that reperfusion of blood under pressure through a small diameter catheter may contribute to hemolysis and possible dislodgment of emboli.[0019]
• In applicant's co-pending U.S. patent application Ser. No. 09/333,074, filed Jun. 14, 1999, which is incorporated herein by reference, applicant described the use of external suction to induce regional reversal of flow. That application further described that intermittently induced regional flow reversal overcomes the drawbacks of naturally-aspirated systems such as described hereinabove. However, the use of external suction may in some instances result in flow rates that are too high to be sustained for more than a few seconds. In addition, continuous use of an external pump may result in excessive blood loss, requiring infusion of non-autologous blood and/or saline that causes hemodilution, reduced blood pressure, or raise related safety issues.[0020]
• In view of these drawbacks of the previously known emboli removal systems, it would be desirable to provide methods and apparatus for removing emboli from within the carotid arteries during interventional procedures, such as angioplasty or carotid stenting, that reduce the risk that emboli are carried into the cerebral vasculature.[0021]
• It also would be desirable to provide methods and apparatus for removing emboli from within the carotid arteries during interventional procedures, such as angioplasty or carotid stenting, that provide substantially continuous low retrograde blood flow from the treatment zone, thereby reducing the risk that emboli are carried into the cerebral vasculature.[0022]
• It further would be desirable to provide emboli removal methods and apparatus that prevent the development of reverse flow from the ECA and antegrade into the ICA once the CCA has been occluded, thereby enhancing the likelihood that emboli generated by a surgical or interventional procedure are effectively removed from the vessel.[0023]
• It still further would be desirable to provide an occlusion balloon on a guide wire for placement in the ECA during stenting of the ICA that mitigates the risk of snagging the stent during removal.[0024]
• It also would be desirable to provide methods and apparatus for removing emboli during a carotid stenting procedure that enable filtering of emboli and reduced blood loss.[0025]
SUMMARY OF THE INVENTION
• In view of the foregoing, it is an object of this invention to provide methods and apparatus for removing emboli from within the carotid arteries during interventional procedures, such as angioplasty or carotid stenting, that reduce the risk that emboli are carried into the cerebral vasculature.[0026]
• It also is an object of the present invention to provide methods and apparatus for removing emboli from within the carotid arteries during interventional procedures, such as angioplasty or carotid stenting, that provide substantially continuous low retrograde blood flow from the treatment zone, thereby reducing the risk that emboli are carried into the cerebral vasculature.[0027]
• It is another object of the present invention to provide emboli removal methods and apparatus that prevent the development of reverse flow between the ECA and ICA once the common carotid artery has been occluded, thereby enhancing the likelihood that emboli generated by a surgical or interventional procedure are effectively removed from the vessel.[0028]
• It is a further object of this invention to provide methods and apparatus for an occlusion balloon on a guide wire for placement in the ECA during stenting of the ICA that mitigates the risk of snagging the stent during removal.[0029]
• It is yet another object of the present invention to provide methods and apparatus for removing emboli during a carotid stenting procedure that enable filtering of emboli and reduced blood loss.[0030]
• The foregoing objects of the present invention are accomplished by providing interventional apparatus comprising an arterial catheter, an occlusion balloon disposed on a guide wire, a venous return catheter, and optionally a blood filter. The arterial catheter has proximal and distal ends, an aspiration lumen extending therebetween, an occlusion element disposed on the distal end, and a hemostatic port and blood outlet port disposed on the proximal end that communicate with the aspiration lumen. The aspiration lumen is sized so that an interventional instrument, e.g., an angioplasty catheter or stent delivery system, may be readily advanced therethrough to the site of a stenosis in either the ECA (proximal to the balloon) or the ICA.[0031]
• In accordance with the principles of the present invention, the arterial catheter is disposed in the CCA proximal of the ICA/ECA bifurcation, the occlusion balloon on the guide wire is disposed in the ECA to occlude flow reversal from the ECA to the ICA, and the blood outlet port of the arterial catheter is coupled to the venous return catheter, with or without the blood filter disposed therebetween. Higher arterial than venous pressure, especially during diastole, permits substantially continuous flow reversal in the ICA during the procedure (other than when a dilatation balloon is inflated), thereby flushing blood containing emboli from the vessel. The blood is filtered and reperfused into the body through the venous return catheter.[0032]
• Methods of using the apparatus of the present invention are also provided.[0033]
BRIEF DESCRIPTION OF THE DRAWINGS
• Further features of the invention, its nature and various advantages will be more apparent from the accompanying drawings and the following detailed description of the preferred embodiments, in which:[0034]
• FIGS. 1A and 1B are schematic views of previously known emboli protection systems;[0035]
• FIG. 2 is a schematic view of the emboli protection system of the present invention;[0036]
• FIGS.[0037]3A-3D are, respectively, a schematic view, and detailed side and sectional views of the distal end of an interventional device of the present invention;
• FIGS. 4A and 4B are views of the distal end of an alternative interventional device suitable for use in the system of the present invention; and[0038]
• FIGS.[0039]5A-5D illustrate a method of using the system of FIG. 3 in accordance with the principles of the present invention;
• FIGS.[0040]6A-6B are, respectively, a schematic view and a cross-sectional view of an alternative embodiment of the device of FIGS. 3;
• FIGS.[0041]7A-7B are, respectively, a schematic view of an alternative embodiment of the guide wire balloon elements of the device of FIGS.3, and a method of using the alternative embodiment.
DESCRIPTION OF THE PREFERRED EMBODIMENTS
• Referring to FIGS. 1A and 1B, drawbacks of previously known emboli removal catheters are described with reference to performing percutaneous angioplasty of stenosis S in common carotid artery CCA.[0042]
• With respect to FIG. 1A, drawbacks associated with naturally-aspirated emboli removal systems, such as described in the above-mentioned patent to Solano and European Patent Publication, are described. No flow reversal is induced by those systems until after balloon[0043]10 of angioplasty catheter11 first is passed across the stenosis, inflated, and then deflated. However, applicant has determined that oncemember15 ofemboli removal catheter16 is inflated, flow within the ECA reverses and provides antegrade flow into the ICA, due to the lower hemodynamic resistance of the ICA. Consequently, emboli E generated while passingguide wire20 or catheter11 across stenosis S may be carried irretrievably into the cerebral vasculature—before flow in the vessel is reversed and directed into the aspiration lumen ofemboli removal catheter16 by opening the proximal end of the aspiration lumen to atmospheric pressure Furthermore, natural-aspiration may not remove an adequate volume of blood to retrieve even those emboli that have not yet been carried all the way into the cerebral vasculature.
• In FIG. 1B,[0044]system17 described in the above-mentioned patent to Imran is shown. As described hereinabove, deployment of distal balloon18, and ejection of blood out of the distal end of the inner catheter, may dislodge emboli from the vessel wall distal to balloon18. The introduction of antegrade flow throughinner catheter19 is expected only to exacerbate the problem by pushing the emboli further into the cerebral vasculature. Thus, while the use of positive suction in the Imran system may remove emboli located in the confined treatment field defined by the proximal and distal balloons, such suction is not expected to provide any benefit for emboli dislodged distal of distal balloon18.
• Referring now to FIG. 2, apparatus and methods of the present invention are described.[0045]Apparatus30 comprisescatheter31 having an aspiration lumen andocclusion element32, and guidewire35 havinginflatable balloon36 disposed on its distal end. In accordance with the principles of the present invention, antegrade blood flow is stopped when bothocclusion element32 in the CCA andinflatable balloon36 are deployed. Furthermore, the aspiration lumen ofcatheter31 is connected to a venous return catheter (described hereinbelow), disposed, for example, in the patient's femoral vein. In this manner a substantially continuous flow of blood is induced between the treatment site and the patient's venous vasculature. Because flow through the artery is towardscatheter31, any emboli dislodged by advancing a guide wire or angioplasty catheter33 across stenosis S causes the emboli to be aspirated bycatheter31.
• Unlike the previously known naturally-aspirated systems, the present invention provides substantially continuous retrograde blood flow through eh ICA while preventing blood from flowing retrograde in the ECA and antegrade into the ICA, thereby preventing emboli from being carried into the cerebral vasculature. Because the apparatus and methods of the present invention “recycle” emboli-laden blood from the arterial catheter through the blood filter and to the venous return catheter, the patient experiences significantly less blood loss.[0046]
• Referring now to FIG. 3A,[0047]embolic protection apparatus40 constructed in accordance with the principles of the present invention is described.Apparatus40 comprisesarterial catheter41,guide wire45,venous return line52,tubing49 andoptional blood filter50.
• [0048]Catheter41 includesdistal occlusion element42, proximalhemostatic port43, e.g., a Touhy-Borst connector,inflation port44, andblood outlet port48.Guide wire45 includesballoon46 that is inflated viainflation port47.Tubing49 couplesblood outlet port48 to filter50 andblood inlet port51 ofvenous return line52.
• [0049]Guide wire45 andballoon46 are configured to pass throughhemostatic port43 and the aspiration lumen of catheter41 (see FIGS. 3C and 3D), so that the balloon may be advanced into and occlude theECA. Port43 and the aspiration lumen ofcatheter41 are sized to permit additional interventional devices, such as angioplasty balloon catheters, atherectomy devices and stent delivery systems to be advanced through the aspiration lumen whenguide wire45 is deployed.
• [0050]Guide wire45 preferably comprises a small diameter flexible shaft having an inflation lumen that couplesinflatable balloon46 toinflation port47.Inflatable balloon46 preferably comprises a compliant material, such as described hereinabove with respect toocclusion element42 ofemboli removal catheter41.
• [0051]Venous return line52 includeshemostatic port53,blood inlet port51 and a lumen that communicates withports53 and51 andtip54.Venous return line52 may be constructed in a manner per se known for venous introducer catheters.Tubing49 may comprise a suitable length of a biocompatible material, such as silicone. Alternatively,tubing49 may be omitted andblood outlet port48 ofcatheter41 andblood inlet port51 ofvenous return line52 may be lengthened to engage either end offilter50 or each other.
• With respect to FIGS. 3B and 3C,[0052]distal occlusion element42 comprises expandable bell or pear-shapedballoon55. In accordance with manufacturing techniques which are known in the art,balloon55 comprises a compliant material, such as polyurethane, latex or polyisoprene which has variable thickness along its length to provide a bell-shape when inflated.Balloon55 is affixed todistal end56 ofcatheter41, for example, by gluing or a melt-bond, so that opening57 inballoon55 leads intoaspiration lumen58 ofcatheter41.Balloon55 preferably is wrapped and heat treated during manufacture so thatdistal portion59 of the balloon extends beyond the distal end ofcatheter41 and provides an atraumatic tip or bumper for the catheter.
• As shown in FIG. 3D,[0053]catheter41 preferably comprisesinner layer60 of low-friction material, such as polytetrafluoroethylene (“PTFE”), covered with a layer of flat stainlesssteel wire braid61 and polymer cover62 (e.g., polyurethane, polyethylene, or PEBAX).Inflation lumen63 is disposed withinpolymer cover62 and couplesinflation port44 toballoon55. In a preferred embodiment ofcatheter41, the diameter oflumen58 is 7 Fr, and the outer diameter of the catheter is approximately 9 Fr.
• Referring now to FIGS. 4A and 4B, an alternative embodiment of[0054]occlusion element42 of the system of FIG. 3A is described. In FIGS. 4A and 4B,occlusion element42 ofemboli removal catheter41 comprises self-expandingwire basket65 covered withelastomeric polymer66, such as latex, polyurethane or polyisoprene. Alternatively, a tightly knit self-expanding wire mesh may be used, with or without an elastomeric covering.
• [0055]Catheter41 is surrounded bymovable sheath67.Catheter41 is inserted transluminally withsheath67 in a distalmost position, and afterbasket65 has been determined to be in a desired position proximal to a stenosis,sheath67 is retracted proximally to causebasket65 to deploy. Upon completion of the procedure,basket65 is again collapsed withinsheath67 by moving the sheath to its distalmost position. Operation of the system of FIG. 3A using the emboli removal catheter of FIGS. 4A and 4B is similar to that described hereinbelow for FIGS.5A-5D, except that the occlusion element self-expands whensheath67 is retracted, rather than by infusing an inflation medium to balloon55.
• Referring now to FIGS.[0056]5A-5D, use of the apparatus of FIGS.3 in accordance with the methods of the present invention is described. In FIGS.5, stenosis S is located in internal carotid artery ICA above the bifurcation between the internal carotid artery ICA and the external carotid artery ECA. In a first step,catheter41 is inserted, either percutaneously and transluminally or via a surgical cut-down, to a position proximal of stenosis S, without causingguide wire45 to cross the stenosis.Balloon55 ofdistal occlusion element42 is then inflated, preferably with a radiopaque contrast solution, viainflation port44. As seen in FIG. 5A, this creates reversal of flow from the external carotid artery ECA into the internal carotid artery ICA.
• [0057]Venous return line52 then is introduced into the patient's femoral vein, either percutaneously or via a surgical cut-down.Filter50 is then coupled betweenblood outlet port48 ofcatheter41 andblood inlet port51 ofvenous return line52 usingtubing49, and any air is removed from the line. Once this circuit is closed, negative pressure in the venous catheter during diastole will establish a low rate continuous flow of blood throughaspiration lumen58 ofcatheter41, as seen in FIG. 5B, to the patient's vein viavenous return line52.
• This low rate continuous flow due to the difference between venous pressure and arterial pressure will continue throughout the interventional procedure. Specifically, blood passes through[0058]aspiration lumen58 andblood outlet port48 ofcatheter41, throughbiocompatible tubing49 to filter50, and intoblood inlet port51 ofvenous return line52, where it is reperfused into the remote vein. Filtered emboli collect infilter50 and may be studied and characterized upon completion of the procedure.
• Continuous blood flow (except during inflation of any dilatation instruments) with reperfusion in accordance with the present invention provides efficient emboli removal with significantly reduced blood loss. Alternatively, filter[0059]50 may be omitted, in which case emboli removed from the arterial side will be introduced into the venous side, and eventually captured in the lungs. Because of a low incidence of septal defects, which could permit such emboli to cross-over to the left ventricle, the use offilter50 is preferred.
• Referring to FIG. 5C, with[0060]balloon55 ofocclusion element42 inflated and a retrograde flow established in the ICA,guide wire45 andballoon46 are advanced throughaspiration lumen58. Whenballoon46 is disposed within the ECA, as determined, e.g., using a fluoroscope and a radiopaque inflation medium injected intoballoon46,balloon46 is inflated. Occlusion of the ECA prevents the development of reverse flow in the ECA from causing antegrade flow in the ICA. Another interventional instrument, such as conventionalangioplasty balloon catheter71 havingballoon72, is loaded throughhemostatic port43 andaspiration lumen58 and positioned within the stenosis.Hemostatic port43 is closed andinstrument71 is actuated to disrupt the plaque forming stenosis S.
• As seen in FIG. 5D, upon completion of the angioplasty portion of the[0061]procedure using catheter71,balloon72 is deflated Throughout the procedure, except when the dilatation balloon is fully inflated, the pressure differential between the blood in the ICA and the venous pressure causes blood in ICA to flow in a retrograde direction in the ICA intoaspiration lumen58 ofemboli removal catheter41, thereby flushing any emboli from the vessel. The blood is filtered and reperfused into the patient's vein.
• Optionally, increased volumetric blood flow through the extracorporeal circuit may by achieved by attaching an external pump, such as a roller pump, to[0062]tubing49. If deemed beneficial, the external pump may be used in conjunction withdevice40 at any point during the interventional procedure.Instrument71,guide wire45,emboli removal catheter41, andvenous return line52 are then removed from the patient, completing the procedure.
• As set forth above, the method of the present invention protects against embolization, first, by preventing the reversal of blood flow from the ECA to the ICA when[0063]distal occlusion element42 is inflated, and second, by providing continuous, low volume blood flow from the carotid artery to the remote vein in order to filter and flush any emboli from the vessel and blood stream. Advantageously, the method of the present invention permits emboli to be removed with little blood loss, because the blood is filtered and reperfused into the patient. Furthermore, continuous removal of blood containing emboli prevents emboli from migrating too far downstream for aspiration.
• Referring now to FIGS.[0064]6,apparatus140 constructed in accordance with the present invention is described.Apparatus140 is an alternative embodiment ofapparatus40 described hereinabove and comprisesarterial catheter141 havingdistal occlusion element142, proximalhemostatic port143,inflation port144 andblood outlet port148.Guide wire145 includesballoon146 that is inflated viainflation port147. Biocompatible tubing149 couplesblood outlet port148 to filter150 and toblood inlet port151 ofvenous return line152.Arterial catheter141,guide wire145,venous return line152 and tubing149 are constructed as described hereinabove, except as noted below.
• [0065]Guide wire145 andballoon146 are configured to pass throughguide wire lumen164 of catheter141 (see FIG. 6B), so that the balloon may be advanced into and occlude the ECA. Additionally,catheter141 comprisesaspiration lumen158 which is sized to permit interventional devices, such as angioplasty balloon catheters, atherectomy devices and stent delivery systems to be advanced throughport143 and the aspiration lumen. As shown in FIG. 6B, the key difference betweencatheters41 and141 lies in the method of advancing the guide wire through the catheter: guidewire45 is advanced through the aspiration lumen ofcatheter41, whereasguide wire145 is advanced through separateguide wire lumen164 ofcatheter141.
• [0066]Catheter141 preferably is constructed frominner layer160 of low-friction material, such as polytetrafluoroethylene (“PTFE”), covered with a layer of flat stainless steel wire braid161, and polymer cover162 (e.g., polyurethane, polyethylene, or PEBAX).Inflation lumen163 is disposed withinpolymer cover162 and couplesinflation port144 toocclusion element142.Guide wire lumen164 also is disposed withinpolymer cover142, and is sized to permitguide wire145 andballoon146 to pass therethrough. In a preferred embodiment ofcatheter141, the diameter ofinflation lumen163 is 0.014″, the diameter ofguide wire lumen164 is 0.020″, and the diameter oflumen158 is 7 Fr. To retain an outer catheter diameter in the preferred embodiment of approximately 9 Fr., the thickness of the catheter wall varies around the circumference from a maximum of 0.026″ at the location ofguide wire lumen164 to a minimum of 0.005″ 180 degrees away.
• Referring now to FIGS.[0067]7, an alternative embodiment of the guide wire occlusion apparatus of the present invention is described.Occlusion apparatus200 comprisesguide wire201,occlusion balloon202, inflation lumen203, andwedge204.Wedge204 may comprise a resilient material, such as a polymer or resilient wire, and reduces the risk thatballoon202 will snag on a stent that extends beyond the bifurcation of the ICA and ECA.
• For the reasons described hereinabove, it is desirable when performing a stenting procedure in the ICA to occlude the ECA, to prevent flow reversal from the ECA and into the ICA. Accordingly, an occlusion balloon on a guide wire is placed in the ECA and inflated to block that artery. A stent then may be placed in the ICA to ensure proper blood flow to the ICA. It is often desirable, however, for such stents to extend beyond the bifurcation between the ECA and the ICA. Consequently, when the occlusion balloon on the guide wire is deflated and withdrawn from the ECA, there is a risk that the balloon may snag the stent. In such cases, emergency surgery is often required to remove the balloon.[0068]
• Referring now to FIG. 7B,[0069]occlusion apparatus200 is illustratively shown in conjunction withcatheter41. Stent S extends beyond the bifurcation between the ECA and the ICA and into the CCA.Balloon202 is deflated and positioned for retrieval. Becauseballoon202 is disposed onguide wire201 instead of a traditional, larger diameter balloon catheter, its cross-sectional diameter is significantly reduced, and thus the risk that the balloon will snag on stent S is reduced.Resilient wedge204 further reduces this risk by urging the balloon outward away from the stent during retrieval ofguide wire201 andballoon202. Alternatively, a separate sheath may be advanced overguide wire201 andocclusion balloon202 to surround those components, and therefore reduce the risk that the occlusion balloon or guide wire will snag the stent.
• While preferred illustrative embodiments of the invention are described above, it will be apparent to one skilled in the art that various changes and modifications may be made. The appended claims are intended to cover all such changes and modifications that fall within the true spirit and scope of the invention.[0070]

Claims (20)

What is claimed is:

1. Apparatus for removing emboli during an angioplasty or stenting procedure, the apparatus comprising:

a catheter having proximal and distal ends, a lumen extending therethrough, and a blood outlet port in communication with the lumen, the catheter adapted to be disposed in a patient's carotid artery;

an occlusion element disposed on the distal end of the catheter and having an opening that communicates with the lumen, the occlusion element having a contracted state suitable for transluminal insertion and an expanded state wherein the occlusion element occludes antegrade flow in the vessel;

a venous return catheter having proximal and distal ends, a lumen extending therethrough, and a blood inlet port in communication with the lumen; and

tubing that couples the blood outlet port to the blood inlet port.

2. The apparatus of

claim 1

further comprising a wire having a distal end and a balloon disposed on the distal end, wherein the wire and balloon are sized to pass through the lumen of the catheter.

3. The apparatus of

claim 1

further comprising a blood filter coupled between the blood outlet port and the blood inlet port.

4. The apparatus of

claim 1

wherein the occlusion element is an inflatable member.

5. The apparatus of

claim 4

wherein the inflatable element has a pear-shape with a wall thickness that varies along the length of the inflatable member.

6. The apparatus of

claim 4

wherein a portion of the pear-shaped inflatable member extends beyond the distal end of the catheter in the contracted position and forms an atraumatic bumper.

7. The apparatus of

claim 1

wherein the occlusion element comprises a self-expanding basket.

8. The apparatus of

claim 1

wherein the catheter comprises:

a non-stick tubular member;

a layer of wire braid disposed surrounding the non-stick tubular member; and

a layer of thermoplastic polymer disposed on the layer of wire braid.

9. The apparatus of

claim 1

wherein the catheter further comprises a second lumen through which the wire and inflatable balloon may be inserted.

10. The apparatus of

claim 1

further comprising a pump that removes blood through the catheter and reperfuses blood via the venous return catheter.

11. The apparatus of

claim 2

further comprising a resilient wedge affixed to the wire proximal of the balloon to reduce snagging of the balloon following a stenting procedure.

12. A method for removing emboli from a vessel comprising:

providing a catheter having proximal and distal ends, a lumen extending therethrough, an occlusion element disposed on the distal end, a hemostatic port coupled to the lumen, and a blood outlet port coupled to the lumen;

providing a venous return catheter having proximal and distal ends, a lumen extending therethrough, and a blood inlet port coupled to the lumen;

inserting the distal end of the catheter to a position proximal to the stenosis;

inserting the distal end of the venous return catheter into a remote vein;

deploying the occlusion element to occlude antegrade flow through the vessel;

causing blood to flow between the blood outlet port and the blood inlet port to induce reverse flow in, and remove emboli from, the vessel.

13. The method of

claim 12

further comprising:

providing a blood filter; and

coupling the blood filter in fluid communication between the blood outlet port and the blood inlet port.

14. The method of

claim 12

further comprising:

providing a wire having a balloon;

while flow is reversed in the vessel, advancing the balloon of the wire into the patient's external carotid artery;

inflating the balloon of the wire to prevent reverse flow from the external carotid artery from entering the internal carotid artery.

15. The method of

claim 12

further comprising, while causing blood to flow between the blood outlet port and the blood inlet port, performing an interventional procedure with an interventional instrument inserted through the hemostatic port.

16. The method of

claim 12

wherein the occlusion element comprises a balloon, and deploying the occlusion element comprises inflating the balloon.

17. The method of

claim 12

wherein the occlusion element comprises a self-expanding basket, and deploying the occlusion element comprises retracting a sheath relative to the distal end of the catheter.

18. The method of

claim 14

wherein advancing the balloon of the wire into the patient's external carotid artery comprises advancing the balloon through a separate lumen of the catheter.

19. The method of

claim 12

further comprising:

providing a pump; and

actuating the pump to increase a rate of flow of blood between the blood outlet port and the blood inlet port.

20. The method of

claim 15

wherein performing an interventional procedure with an interventional instrument comprises delivering a stent within the vessel and the wire further comprises a resilient wedge, the method further comprising urging the resilient wedge against the stent during removal of the wire and balloon.

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