Selectable eccentric remodeling and/or ablation

Abstract
A catheter and catheter system for eccentric remodeling and/or removal of atherosclerotic material of a blood vessel of a patient include an elongate flexible catheter body with a radially expandable structure. A plurality of electrodes or other electrosurgical energy delivery surfaces can radially engage atherosclerotic material when the structure expands. An atherosclerotic material detector near the distal end of the catheter body may measure circumferential atherosclerotic material distribution, and a power source selectively energizes the electrodes to eccentrically remodel the measured atherosclerotic material.
Description
STATEMENT AS TO RIGHTS TO INVENTIONS MADE UNDER FEDERALLY SPONSORED RESEARCH OR DEVELOPMENT

Not Applicable


REFERENCE TO A “SEQUENCE LISTING,” A TABLE, OR A COMPUTER PROGRAM LISTING APPENDIX SUBMITTED ON A COMPACT DISK

Not Applicable


BACKGROUND OF THE INVENTION
1. Field of the Invention

The present invention is generally related to medical devices, systems, and methods. In an exemplary embodiment, the invention provides catheter-based remodeling and/or removal of atherosclerosis plaque built-up in an artery to improve blood flow, often without balloon angioplasty, stenting, and/or dilation. The structures of the invention allow image-guided eccentric atherosclerotic material remodeling and/or removal typically using electrosurgical energy, optionally using electrosurgical ablation, often in a controlled environment zone within the blood vessel, and ideally with a co-located intravascular imaging capability. Related embodiments have applications in a variety of body lumens, including urinary, reproductive, gastrointestinal, and pulmonary obstructive material removal, optionally for removing or decreasing tumors, cysts, polyps, and the like.


Physicians use catheters to gain access to and repair interior tissues of the body, particularly within the lumens of the body such as blood vessels. For example, balloon angioplasty and other catheters often are used to open arteries that have been narrowed due to atherosclerotic disease.


Balloon angioplasty is often effective at opening an occluded blood vessel, but the trauma associated with balloon dilation can impose significant injury, so that the benefits of balloon dilation may be limited in time. Stents are commonly used to extend the beneficial opening of the blood vessel.


Stenting, in conjunction with balloon dilation, is often the preferred treatment for atherosclerosis. In stenting, a collapsed metal framework is mounted on a balloon catheter which is introduced into the body. The stent is manipulated into the site of occlusion and expanded in place by the dilation of the underlying balloon. Stenting has gained widespread acceptance, and produces generally acceptable results in many cases. Along with treatment of blood vessels (particularly the coronary arteries), stents can also be used in treating many other tubular obstructions within the body, such as for treatment of reproductive, gastrointestinal, and pulmonary obstructions.


Restenosis or a subsequent narrowing of the body lumen after stenting has occurred in a significant number of cases. More recently, drug coated stents (such as Johnson and Johnson's Cypher™ stent, the associated drug comprising Sirolimus™) have demonstrated a markedly reduced restenosis rate, and others are developing and commercializing alternative drug eluting stents. In addition, work has also been initiated with systemic drug delivery (intravenous or oral) which may also improve the procedural angioplasty success rates.


While drug eluting stents appear to offer significant promise for treatment of atherosclerosis in many patients, there remain many cases where stents either cannot be used or present significant disadvantages. Generally, stenting leaves an implant in the body. Such implants can present risks, including mechanical fatigue, corrosion, and the like, particularly when removal of the implant is difficult and involves invasive surgery. Stenting may have additional disadvantages for treating diffuse artery disease, for treating bifurcations, for treating areas of the body susceptible to crush, and for treating arteries subject to torsion, elongation, and shortening.


A variety of modified restenosis treatments or restenosis-inhibiting occlusion treatment modalities have also been proposed, including intravascular radiation, cryogenic treatments, ultrasound energy, and the like, often in combination with balloon angioplasty and/or stenting. While these and different approaches show varying degrees of promise for decreasing the subsequent degradation in blood flow following angioplasty and stenting, the trauma initially imposed on the tissues by angioplasty remains problematic.


A number of alternatives to stenting and balloon angioplasty so as to open stenosed arteries have also been proposed. For example, a wide variety of atherectomy devices and techniques have been disclosed and attempted. Despite the disadvantages and limitations of angioplasty and stenting, atherectomy has not gained the widespread use and success rates of dilation-based approaches. Still further disadvantages of dilation have come to light. These include the existence of vulnerable plaque, which can rupture and release materials that may cause myocardial infarction or heart attack.


In light of the above, it would be advantageous to provide new devices, systems, and methods for remodeling and/or removal of atherosclerotic material and other occlusions of the lumens of the body, and particularly from blood vessels. It would further be desirable to enable the removal of these occlusive materials without having to resort to the trauma of a dilation, and to allow the opening of blood vessels and other body lumens which are not suitable for stenting.


BRIEF SUMMARY OF THE INVENTION

In a first non-limiting embodiment, there is a catheter system for eccentric remodeling of atherosclerotic material of a blood vessel of a patient. The system comprises an elongate flexible catheter body having a proximal end and a distal end with an axis therebetween. A radially expandable structure is disposed near the end of the catheter body, and a plurality of energy delivery surfaces are each oriented radially when the expandable structure expands. An atherosclerotic material detector is disposed for circumferential atherosclerotic material detection. A power source is electrically coupled to the energy delivery surfaces. The power source energizes the energy delivery surfaces so as to eccentrically remodel the detected atherosclerotic material.


The power source will often selectively energize a subset of the energy delivery surfaces so as to effect eccentric remodeling. The catheter body may have a lumen extending between the proximal and distal ends, and an aspiration connector may be in fluid communication with the lumen at the proximal end of the catheter body. Proximal and distal debris barriers may be disposed proximally and distally of the energy delivery surfaces, respectively, and an aspiration port may be disposed between the proximal and distal barriers for removal of debris during atherosclerotic material remodeling.


The atherosclerotic material detector may include an intravascular ultrasound catheter disposed in the lumen of the catheter body, an intravascular optical coherence tomography catheter disposed in the lumen, an intravascular catheter having an MRI antenna disposed in the lumen, or the like. Alternative detectors may employ any of a variety of non-invasive imaging modalities, including external systems making use of X-rays, CT systems, non-invasive MRI or NMR systems, or the like, so that the detector may not be disposed in the blood vessel. In some embodiments, a brachytherapy catheter or other restenosis inhibitor may be advanced distally within the lumen.


The radially expandable body may comprise a plurality of flexible struts, and the energy delivery surfaces may define a circumferentially oriented array, with the energy delivery surfaces often comprising electrodes or microwave antennas. Struts of the radially expandable structure may have perforations disposed therebetween so as to define an expandable basket. The basket may have proximal and distal portions with intermediate portion disposed therebetween. The array of electrodes may be supported along the intermediate portion so as to engage adjacent atherosclerotic material when the basket is expanded within the blood vessel. The electrodes may comprise conductive surfaces of an electrode structure mounted to a separately formed basket strut. In other embodiments, electrode surfaces may be formed as part of the expandable structure. For example, the electrodes may comprise a localized widening of an associated strut, often disposed near center of a length of the strut. The expandable structure may comprise Nitinol™, and the remaining surface of the Nitinol strut may be insulated. For example, the surface may be coated with a high temperature polymer (such as a polyimide or the like). Other coatings may alternatively be used, including polyurethane. The struts may be electrically insulated from each other, so that each strut can be used to conduct energy to an electrode surface associated with the strut from a conductor extending proximally from the strut so as to independently couple each electrode surface to a controller.


A distal membrane may be deployable within the blood vessel distally of the electrode so as to inhibit distal movement of debris. A proximal membrane may be deployable proximally of the electrode so as to inhibit proximal movement of the debris. The membranes may inhibit blood interaction with the remodeling process, for example, during ablation of the atherosclerotic material. In other embodiments, power supplied to the energy delivery surfaces may be limited so as to inhibit debris generation, for example, by denaturing the atherosclerotic material, by melting of atherosclerotic material inside layers of the artery, by shrinking of atherosclerotic material inside layers of the artery (during treatment and/or in a tissue healing response), and the like. In some embodiments, the distal membrane may be supported by the distal portion of the basket so as to expand radially therewith. The proximal membrane may be supported by the proximal portion of the basket so as to expand radially therewith. At least one of the proximal and distal membranes may comprise a lumen axially off-set from the basket.


While some embodiments may have a single monopolar electrode or two or more monopolar or bipolar electrodes, the electrodes may comprise an array of at least three alternatively selectable electrodes distributed circumferentially about the axis, often comprising six or more electrodes. A controller may couple the power source to the electrode array so as to selectively energize that eccentric subset of the electrode array in response to the detected atherosclerotic material. A controller may selectively energize a subset of the energy directing surfaces by directing RF energy and/or microwave energy thereto. The atherosclerotic material detector may comprise an ultrasound transducer or optical coherence reflectrometer. Along with stand-alone structures that are insertable into a lumen of the catheter, these detectors may also be integrated into the catheter structure. A display may be coupled to the atherosclerotic material detector to show an image of circumferential atherosclerotic material thickness distributed about the catheter axis.


In another non-limiting embodiment, there is a catheter system for eccentric remodeling and/or removal of atherosclerotic material from a blood vessel of a patient. The system comprises an elongate flexible catheter body having a proximal end and a distal end with an axis therebetween. A radially expandable structure is disposed near the distal end of the catheter body. A plurality of electrodes are oriented to be radially urged against atherosclerotic material when the expandable structure expands. An atherosclerotic material detector or imaging sensor is disposed near the distal end of the catheter body for circumferential identification and measurement of atherosclerotic material. A power source is electrically coupled to the electrodes. The power source energizes the electrodes so as to eccentrically remove and/or ablate the measured atherosclerotic material.


The catheter body will often have a lumen extending between the proximal end and the distal end. The lumen may be used as an aspiration lumen, for example, using an aspiration source in fluid communication with the lumen at the proximal end of the catheter body. Proximal and distal ablation debris barriers may be disposed proximally and distally of the electrodes, respectively, with an aspiration port disposed between the proximal and distal barriers for removal of ablation debris during atherosclerotic material ablation. The atherosclerotic material detector may comprise an ultrasound transducer of an intravascular ultrasound catheter, with the intravascular ultrasound catheter disposed in the lumen. Alternatively, other imaging modalities may be employed, including intravascular optical coherence tomography. Imaging or atherosclerotic material detecting capabilities might also be incorporated into the catheter body in some embodiments, with circumferential atherosclerotic thicknesses often being measured. An irrigation lumen may extend between the proximal end of the catheter body and the distal end of the catheter body, facilitating an enhanced local ablation environment adjacent the electrodes. A restenosis inhibitor may be advanced within the lumen, the restenosis inhibitor optionally comprising an intravascular radiation catheter, restenosis inhibiting drugs, or the like.


The radially expandable body may comprise a plurality of flexible members or struts, the electrodes optionally defining a circumferential electrode array. The struts may have perforations or openings therebetween so as to define an expandable basket. The array of electrodes may be supported along an intermediate portion of the basket and oriented radially so as to engage adjacent atherosclerotic material when the basket is expanded within a blood vessel. An aspiration port in fluid communication with an interior of the basket may facilitate removal of any ablation debris and tissue vaporization gasses, and may inhibit release of these byproducts of ablation within the blood vessel, and fluid flowing within the basket may act as a cooling fluid to limit collateral tissue damage. A distal membrane or barrier deployable within the blood vessel distally of the electrodes may inhibit distal movement of any ablation debris, while a proximal membrane or membrane deployable proximally of the electrodes may inhibit proximal movement of any ablation debris. Such member(s) may also reduce or inhibit blood flow within a localized remodeling and/or ablation environment. The distal membrane may be supported by the distal portion of the basket so as to expand radially therewith, and/or the proximal membrane may be supported by the proximal portion of the basket so as to expand radially therewith. Suitable membranes include, for example, one or more balloons axially offset from the basket within the blood vessel, or a braided superelastic material such as Nitinol™ dipped in silicone, polyurethane, PTFE, or another elastic material. In some embodiments, the membrane may be at least in part integrated with the basket.


The electrodes will often comprise an array of at least three, often comprising at least six alternatively selectable electrodes distributed circumferentially about the axis of the catheter body. The arrays of electrodes may be axisymmetric, with an eccentric treatment orientation being selected without physically rotating the array by selectively pairing electrodes of the array. A controller couples the power source to the electrode array for selectively energizing an eccentric subset of the electrode array in response to the measured atherosclerotic material. Exemplary electrodes may comprise stainless steel soldered to copper wires, with the copper wires insulated from supporting elements of associated expandable basket elements. Alternative electrodes may comprise platinum (which also allows the electrode to serve as a radiopaque marker). The electrode/basket assembly may be, for example, coated with a high temperature polymer, such as a polyimide. An exemplary electrode array includes alternating axially offset electrodes, and the controller will often direct RF bipolar power between pairs of the energized subset of electrodes, the pairs optionally comprising circumferentially offset electrodes, adjacent axially aligned electrodes, or alternating between axially and circumferentially offset electrodes. In some embodiments monopolar energy may be directed to selected electrodes, with the circuit being completed by a patient ground. More generally, each electrode will typically comprise a metallic body affixed to an adjacent strut of the expandable structure by a polymer with an associated conductor extending proximally from the electrode so as to electrically couple the electrode surface to the controller.


One exemplary atherosclerotic material detector may include an ultrasound transducer of an intravascular ultrasound catheter, a sensor of an intravascular optical coherence tomography catheter, or the like. A display may be provided to show an image of circumferential sclerotic material thickness about the catheter axis, the display and/or imaging catheter signals optionally comprising indicia of orientation for rotationally registering the selected electrodes to the measurements. Suitable indicia may comprise a “key” or distinguishable image of at least one expandable member or marker.


In another non-limiting embodiment, there is a catheter for atherosclerotic material removal from the blood vessel of a patient. The catheter comprises an elongate flexible catheter body having a proximal end and a distal end with an axial aspiration lumen therebetween. A radially expandable basket near the distal end of the catheter body has a proximal portion and a distal portion with an intermediate portion disposed therebetween. A circumferential electrode array is distributed about the intermediate portion of the radially expandable basket so as to ablate adjacent atherosclerotic material when the basket expands within the blood vessel. An aspiration port provides fluid communication between the aspiration lumen and an interior of the basket. A distal membrane supported by the distal portion of the basket inhibits distal movement of ablation debris when the basket is expanded within the blood vessel. A proximal membrane supported by the proximal portion of the basket inhibits proximal movement of ablation debris when the basket is expanded within the blood vessel.


One non-limiting embodiment of a method is a method for remodeling eccentric atherosclerotic material of a blood vessel of a patient. The method comprises positioning a working end of a catheter within the blood vessel adjacent the atherosclerotic material, the catheter defining an axis. The catheter is radially expanded so as to engage at least one energy delivery surface of the catheter against the atherosclerotic material. A circumferential distribution of the atherosclerotic material about the axis of the catheter is determined. Electrosurgical energy is directed from the at least one energy delivery surface eccentrically relative to the axis of the catheter in response to the determined atherosclerotic material distribution.


Remodeling of the atherosclerotic material may comprise ablation, removal, shrinkage, melting, denaturing, and/or the like of the atherosclerotic material. For example, relatively low power RF energy may be used to heat the atherosclerotic material until it melts, the material optionally being redistributed along the artery wall, inside layers of the vessel, or the like. Optionally, the atherosclerotic material may comprise a vulnerable plaque. Vulnerable plaques (and/or blood vessels in which vulnerable plaque is a concern) may be treated using RF energy to mildly heat the cap and underlying lipid-rich pool of the vulnerable plaque to a temperature in a range from about 50 to about 60° Celsius. This may be performed so as to generate thickening of the cap, often as an immune response to heating. Such thickening may potentially result in restenosis, and cap thickening and/or restenosis may be limited by accurate control of the RF energy, the use of anti-restenotic drugs (such as Rapamycin™ or the like). In addition to vulnerable plaque stabilization, the invention may be employed to eliminate vulnerable plaques, optionally by heating of the lipid-rich pool to a temperature of at least around 90° Celsius. Preferably, heating of the blood vessel will be performed so as to limit a temperature of an adventitia or outer layer of the blood vessel to below about 63° Celsius so as to inhibit collagen shrinkage and vessel collapse. In contrast, mild RF energy may be applied to the atherosclerotic material so as to denature the material and result in shrinkage of the material during or after treatment. Shrinkage of atherosclerotic material may lead to larger open vessel lumens and improved blood flow.


When remodeling of atherosclerotic plaques comprises ablation of atherosclerotic materials, any thrombolitic debris generated may be restrained and/or evacuated. Where ablation generates non-thrombolitic debris, or where remodeling is performed so as to inhibit debris generation, debris restraining and evacuation may be unnecessary.


Electrosurgical energy directed by the one or more energy delivery surfaces will often comprise RF and/or microwave electrical energy. The circumferential distribution of atherosclerotic material may be determined using intravascular or non-invasive techniques. The electrosurgical energy may be directed eccentrically without rotating the energy delivery surfaces about the catheter axis by energizing a subset of the electrodes. The subset of electrodes may be selected in response to the determined atherosclerotic material distribution. Selected electrodes may be rotationally registered with the atherosclerotic material distribution, for example, with reference to one or more structures of the expandable basket having a distinguishable image. For example, a strut of the electrode arbitrarily identified as electrode 1 may have one radiopaque marker or other distinguishable image, and a strut of an electrode referenced as electrode 2 may have two radiopaque markers or two distinguishable image features. This can help identify all of the electrodes, since electrode 1 is identifiable and the direction from electrode 1 to electrode 2 indicates a circumferential electrode count direction. A variety of alternative distinguishable features with integrated or separate circumferential electrode count orientation indicators may also be utilized. In some embodiments, registration may be performed automatically with reference to an electronic signal.


In yet another non-limiting embodiment, there is a method for eccentric atherosclerotic material removal from a blood vessel of a patient. The method comprises positioning a working end of the catheter within the blood vessel and adjacent the atherosclerotic material. The catheter defines the axis. The catheter is radially expanded so as to engage a plurality of electrodes of the catheter against the atherosclerotic material. A circumferential distribution of the atherosclerotic material is measured about the axis of the catheter. RF energy is directed from the electrodes eccentrically relative to the axis of the catheter in response to the measured atherosclerotic material distribution.





BRIEF DESCRIPTION OF THE DRAWINGS


FIG. 1A illustrates diffuse atherosclerotic disease in which a substantial length of multiple blood vessels has limited effective diameters.



FIG. 1B illustrates vulnerable plaque within a blood vessel.



FIG. 1C illustrates the sharp bends or tortuosity of some blood vessels.



FIG. 1D illustrates atherosclerotic disease at a bifurcation.



FIG. 1E illustrates a lesion associated with atherosclerotic disease of the extremities.



FIG. 1F is an illustration of a stent fracture or corrosion.



FIG. 1G illustrates a dissection within a blood vessel.



FIG. 1H illustrates a circumferential measurement of an artery wall around a healthy artery.



FIG. 1I illustrates circumferential distribution of atheroma about a restenosed artery.



FIG. 2 schematically illustrates an atherosclerotic material catheter system according to the present invention.



FIG. 2A schematically illustrates a catheter system for remodeling atherosclerotic material, the system including the catheter of FIG. 2.



FIG. 3 illustrates an expandable basket and an associated electrode array of the catheter system of FIG. 2.



FIGS. 4 and 5 illustrate alternative basket structures for use with the catheter system of FIG. 2.



FIGS. 6A and 6B illustrate an exemplary basket structure having alternating axially offset electrodes in a circumferential array.



FIGS. 7A and 7B illustrate an exemplary ablation debris barrier for use with a basket.



FIG. 7C illustrates an alternative basket and debris barrier.



FIG. 8 illustrates electrodes having dedicated conductors mounted to associated elements of a superelastic metal basket.



FIG. 9 is an illustration of a basket comprising polyimide supporting a circumferential array of electrodes.



FIGS. 10A-E illustrate an exemplary atherosclerotic material remodeling and/or removal method using the catheter system of FIG. 2.



FIGS. 11-21 schematically illustrate alternative catheters and catheter systems for use in the methods described herein.



FIGS. 22-25 schematically illustrate controllers for selectively energizing electrodes in the system of FIG. 2.



FIGS. 26 and 27 schematically illustrate alternative fluid flow paths for use in an atherosclerotic material remodeling catheter.



FIGS. 28A-28D illustrate an alternative controller for selectively energizing electrodes in the system of FIG. 2.



FIGS. 29A-29H illustrate an alternative basket structure formed with independent struts having a localized enhanced width for use as an electrode surface, along with components thereof.



FIGS. 30A and 30B schematically illustrate electrical circuitry allowing thermocouples and other temperature sensors to be used both for measuring temperature and as electrodes.



FIG. 31 schematically illustrates an alternative catheter structure for use in the methods described herein.



FIGS. 32A-32D schematically illustrate alternative basket and catheter structures for use in the methods described herein.



FIG. 33 schematically illustrates an alternative catheter structure using microwave energy to remodel atherosclerotic material.



FIG. 34 schematically illustrates an alternative catheter structure having lumens extending toward the electrodes so as to provide directed irrigation flow in the methods described herein.



FIG. 35 schematically illustrates a further alternative catheter basket structure having lumens for directing irrigation flow toward the microwave antennas for use in the methods described herein.



FIG. 36 is a schematic cross sectional view showing the application of different power levels through different electrodes so as to eccentrically remodel atherosclerotic materials.



FIGS. 37A-37C illustrate a further alternative catheter basket structure, in which the basket comprises polyimide for supporting a circumferential array of electrodes and facilitating intravascular imaging.



FIGS. 38A-38E are cross sectional side views through a body lumen showing additional aspects of treatment methods and devices described herein.



FIGS. 38F-38H are cross sectional views taken across a body lumen and treatment device to show additional aspects of the eccentric treatment methods and devices.



FIGS. 39A and 39B illustrate an eccentric treatment device and method in a gelatin artery model.



FIG. 40 is a perspective view of an exemplary catheter assembly.





DETAILED DESCRIPTION OF THE INVENTION

Non-limiting embodiments of the present invention provide devices, systems, and methods to remodel a partially occluded artery in order to open the artery lumen and increase blood flow. Remodeling may involve the application of electrosurgical energy, typically in the form of RF and/or microwave electrical potentials to energy delivery surfaces such as electrodes, antennas, and the like. This energy will often be controlled so as to limit a temperature of target and/or collateral tissues, for example, limiting the heating of a fibrous cap of a vulnerable plaque or the intimal layer of an artery structure to a maximum structure in a range from about 50 to about 60° Celsius, by limiting the maximum temperature of an outer layer or adventitia of the blood vessel to no more than about 63° Celsius, limiting heating of a lipid-rich pool of a vulnerable plaque sufficiently to induce melting of the lipid pool while inhibiting heating of other tissues (such as an intimal layer or fibrous cap) to less than a temperature in a range from about 50 to about 60° Celsius so as to inhibit an immune response that might otherwise lead to restenosis, or the like. Relatively mild heating energies may be sufficient to denature and shrink atherosclerotic material during treatment, immediately after treatment, and/or more than one hour, more than one day, more than one week, or even more than one month after the treatment through a healing response of the tissue to the treatment so as to provide a bigger vessel lumen and improved blood flow.


In some embodiments, remodeling of the atherosclerotic plaque may comprise the use of higher energies to ablate and remove occlusive material from within body lumens, and particularly to remove atherosclerotic material from a blood vessel in order to improve blood flow. Ablation debris may be generated by such ablation, and the ablation debris may be thrombolitic or non-thrombolitic. Where thrombolitic debris is generated by ablation, that debris may be restrained, captured, and/or evacuated from the treatment site. Non-thrombolitic debris produced by ablation may not have to be restrained and/or evacuated from the vessel. The techniques of the invention will often provide electrosurgical capabilities, sensing or imaging suitable for measuring atheroma and/or vascular walls, and/or an emboli inhibitor. As atherosclerosis may be eccentric relative to an axis of the blood vessel over 50% of the time, possibly in as much as (or even more than) 75% of cases, the devices and methods of the present invention will often be particularly well suited for directing treatment eccentrically, often in response to circumferential atherosclerotic material detecting or imaging. While the methods and devices described herein allow such eccentric treatments, the devices can also be used for treatment of radially symmetric atherosclerosis by selectively directing energy in a radially symmetric pattern about an axis of the catheter or the like.


Hence, remodeling of atherosclerotic materials may comprise ablation, removal, shrinkage, melting, and the like of atherosclerotic and other plaques. Optionally, atherosclerotic material within the layers of an artery may be denatured so as to improve blood flow, so that debris will not necessarily be generated. Similarly, atherosclerotic materials within the arterial layers may be melted and/or treatment may involve a shrinking of atherosclerotic materials within the artery layers, again without necessarily generating treatment debris. The invention may also provide particular advantages for treatment of vulnerable plaques or blood vessels in which vulnerable plaque is a concern. Such vulnerable plaques may comprise eccentric lesions, and the present invention may be particularly well suited for identifying an orientation (as well as axial location) of the vulnerable plaque structure. The invention will also find applications for targeting the cap structure for mild heating (to induce thickening of the cap and make the plaque less vulnerable to rupture) and/or heating of the lipid-rich pool of the vulnerable plaque (so as to remodel, denature, melt, shrink, and/or redistribute the lipid-rich pool.


While the present invention may be used in combination with stenting and/or balloon dilation, the present invention is particularly well suited for increasing the open diameter of blood vessels in which stenting and balloon angioplasty are not a viable option. Potential applications include treatment of diffuse disease, in which atherosclerosis is spread along a significant length of an artery rather than being localized in one area. The invention may also provide advantages in treatment of vulnerable plaque or blood vessels in which vulnerable plaque is a concern, both by potentially identifying and avoiding treatment of the vulnerable plaque with selected eccentric and/or axial treatments separated from the vulnerable plaque, and by intentionally ablating and aspirating the cap and lipid-rich pool of the vulnerable plaque within a controlled environmental zone or region within the blood vessel lumen. The invention may also find advantageous use for treatment of tortuous, sharply-curved vessels, as no stent need be advanced into or expanded within the sharp bends of many blood vessel. Still further advantageous applications include treatment along bifurcations (where side branch blockage may be an issue) and in the peripheral extremities such as the legs, feet, and arms (where crushing and/or stent fracture failure may be problematic).


Diffuse disease and vulnerable plaque are illustrated in FIGS. 1A and 1B, respectively. FIG. 1C illustrates vascular tortuosity. FIG. 1D illustrates atherosclerotic material at a bifurcation, while FIG. 1E illustrates a lesion which can result from atherosclerotic disease of the extremities.



FIG. 1F illustrates a stent structural member fracture which may result from corrosion and/or fatigue. Stents may, for example, be designed for a ten-year implant life. As the population of stent recipients lives longer, it becomes increasingly likely that at least some of these stents will remain implanted for times longer than their designed life. As with any metal in a corrosive body environment, material degradation may occur. As the metal weakens from corrosion, the stent may fracture. As metal stents corrode, they may also generate foreign body reaction and byproducts which may irritate adjoining body tissue. Such scar tissue may, for example, result in eventual reclosure or restenosis of the artery.


Arterial dissection and restenosis may be understood with reference to FIGS. 1G through 1I. The artery comprises three layers, an endothelial layer, a medial layer, and an adventitial layer. During angioplasty, the inside layer may delaminate or detach partially from the wall so as to form a dissection as illustrated in FIG. 1G. Such dissections divert and may obstruct blood flow. As can be understood by comparing FIGS. 1H and 1I, angioplasty is a relatively aggressive procedure which may injure the tissue of the blood vessel. In response to this injury, in response to the presence of a stent, and/or in the continuing progression of the original atherosclerotic disease, the opened artery may restenose or subsequently decrease in diameter as illustrated in FIG. 1I. While drug eluting stents have been shown to reduce restenosis, the efficacy of these new structures several years after implantation has not be fully studied, and such drug eluting stents are not applicable in many blood vessels.


In general, the present invention provides a catheter which is relatively quick and easy to use by the physician. The catheter system of the present invention may allow arteries to be opened to at least 85% of their nominal or native artery diameter. In some embodiments, arteries may be opened to about 85%, and/or acute openings may be less than 85%. Rapid occlusive material removal may be effected using sufficient power to heat tissues locally to over about 100° C. so as to vaporize tissues, or more gentle remodeling may be employed.


The desired opening diameters may be achieved immediately after treatment by the catheter system in some embodiments. Alternatively, a milder ablation may be implemented, for example, providing to no more than a 50% native diameter when treatment is complete, but may still provide as much as 80 or even 85% or more native vessel open diameters after a subsequent healing process is complete, due to resorption of injured luminal tissues in a manner analogous to left ventricular ablation for arrhythmia and transurethral prostate (TURP) treatments. Such embodiments may heat at least some occlusive tissue to a temperature in a range from about 55° C. to about 80° C. In some embodiments, occlusive tissues may be heated to a maximum temperature in a range between about 93 and 95° C. In other embodiments described herein, heating may be controlled so as to provide tissue temperatures in a range between about 50 and 60° C., with some embodiments benefiting from maximum tissue temperatures of about 63° C. Still further treatments may benefit from treatment temperatures of about 90° C. Advantageously, the catheter systems and methods of the invention may be used without balloon angioplasty, thereby avoiding dissections and potentially limiting restenosis.


An exemplary catheter system 10 is schematically illustrated in FIGS. 2 and 2A. A remodeling and/or ablation catheter 12 includes a catheter body 14 having a proximal end 16 and a distal end 18. Catheter body 14 is flexible and defines a catheter axis 20, and includes an aspiration lumen 22 and an irrigation lumen 24 (see FIG. 3). Still further lumens may be provided for a guidewire, imaging system, or the like as described below. Lumen 22 may be used for sensing and/or imaging of atheroma as well as aspiration.


Catheter 12 includes a radially expandable structure 26 adjacent distal end 18 and a housing 28 adjacent proximal end 16. A distal tip 30 may include an integral tip valve to seal aspiration lumen 22 and allow passage of guidewires, imaging and/or restenosis inhibiting catheters, and the like.


Proximal housing 28 includes a first connector 32 in fluid communication with aspiration lumen 22. Aspiration lumen 22 may have an aspiration port within expandable structure 26 so as to allow aspiration or aspiration of debris and gasses from within the expandable structure. Aspiration lumen 22 may also be used as an access lumen for guidewires, intravascular imaging catheters, and/or distally advancing intravascular radiation treatment catheters or restenosis inhibiting drugs. Hence, connector 32 may selectively accommodate an imaging catheter 34 having an atherosclerotic material detector 36 advancable within catheter body 14 adjacent to and/or beyond distal end 18, the detector often comprising an intravascular ultrasound transducer, an optical coherent tomography sensor, an MRI antenna, or the like. An imaging connector 38 of imaging catheter 34 transmits imaging signals allowing circumferential measurement of atherosclerotic thicknesses about axis 20 to a display 39.


Connector 32 also accommodates a restenosis inhibiting treatment catheter 40, the treatment catheter here comprising an intravascular radiation catheter. Such a radiation catheter may include a radiation source 42 which can again be advanced distally within catheter body 14 to or beyond expandable structure 26.


A second connector 44 of proximal housing 28 is in fluid communication with irrigation lumen 24 (see FIG. 3). Second connector 44 may be coupled to an irrigation fluid source for introducing conductive or non-conductive liquids, gases, or the like, ideally for introducing gas or heparinized saline. Both first and second connectors 32, 44 may optionally comprise a standard connector such as a Luer-Loc™ connector. In FIG. 2A connector 44 is schematically shown coupled to an aspiration vacuum source/infusion fluid source 45.


Referring now to FIGS. 2, 2A, and 3, proximal housing 28 also accommodates an electrical connector 46. Connector 46 includes a plurality of electrical connections, each electrically coupled to an electrode 50 via a dedicated conductor 52. This allows a subset of electrodes 50 to be easily energized, the electrodes often being energized with bipolar or monopolar RF energy. Hence, electrical connector 46 will often be coupled to an RF generator via a controller 47, with the controller allowing energy to be selectively directed to an eccentric portion of an engaged luminal wall. When monopolar RF energy is employed, patient ground may (for example) be provided by an external electrode or an electrode on catheter body 14. A processor 49 may manipulate signals from imaging catheter 34 to generate an image on display 39, may coordinate aspiration, irrigation, and/or treatment, and may automatically register the treatment with the image.


Expandable structure 26 is illustrated in more detail in FIG. 3. Expandable structure 26 may expand resiliently when released from within a restraining sheath, or may expand by pulling tip 30 toward distal end 18 (see FIG. 2), optionally using a pullwire, an inner catheter body 58, or the like. Expandable structure 26 here comprises a perforate structure or basket having a series of structural struts or elements 54 with opening or perforations 56 therebetween. Perforations 56 may be formed, for example, by cutting elongate slits in a flexible tube material, or the basket may be formed by braiding elongate wires or ribbons or the like.


Expandable structure 26 generally includes a proximal portion 60, a distal portion 62, and an intermediate portion 64 therebetween. Each electrode 50 is mounted on an associated basket element 54 along intermediate portion 64, with an associated conductor 52 extending proximally from the electrode. Electrodes 50 are distributed circumferentially about axis 20 in an array, adjacent electrodes preferably being axially offset, ideally being staggered or alternating between proximal and distal axial locations. This allows bipolar energy to be directed between adjacent circumferential (axially offset) electrodes between adjacent distal electrodes, between adjacent proximal electrodes, and the like.


In the exemplary embodiment, proximal and distal barriers 66, 68 expand radially with proximal and distal portions 60, 62 of expandable structure 26. Barriers 66, 68 inhibit any ablation debris and gases generated adjacent electrodes 50 from traveling within the body lumen beyond catheter 12. Barriers 66, 68 also allow an at least partially isolated ablation environment to be established within the body lumen, for example, by replacing blood within a blood vessel with a more advantageous fluid environment for limiting charring of the electrodes and the like. Alternative barriers may be provided instead of (or in combination with) barriers 66, 68, including one or more balloons axially offset from expandable member 26, elastic lips as shown in FIG. 11-13, or the like. In other embodiments remodeling may be effected without generating significant thermolytic ablation debris and/or a desired treatment environment may be provided with localized irrigation and/or aspiration flows so that some systems may forego the use of barriers.


Referring now to FIGS. 4 and 6A, alternative embodiments may use different expandable structures in the form of different baskets. In FIG. 4, a braided basket 70 includes electrodes 50 mounted on braided structures 72. While metallic braided structures may be used in some embodiments with attention to electrical isolation of the electrodes, shorting of crossing metallic braided structures may be problematic. Hence, braided members 72 may comprise a high-temperature polymer or non-conductive material such as polyimide. An elongate electrode basket 76 may include electrodes 50 formed, for example, by selectively exposing a metallic surface along a central portion of basket member 78, while the remainder of the basket element is electrically isolated using a high-temperature polymer or the like so that the basket struts may be used as a conductor for energizing the electrode. Radial expansion of basket 76 is also illustrated by movement 71 of inner catheter body 58 relative to body 14. Expansion may also be effected by withdrawing a sleeve from over the basket, a pull wire, or the like. An intravascular ultrasound image sensor 36 of imaging catheter 34 is illustrated in FIG. 5 distal of expandable structures 76, with a proximal portion of the imaging catheter removed for clarity. Still further alternative expandable structures may be employed, including systems in which an array of electrodes is mounted circumferentially about a balloon, which may reduce blood contamination in the ablation area. Alternatively, a controlled ablation environment may be maintained with barriers proximally and/or distally of the expandable member by axially offset balloons, with an optional aspiration port again being disposed between such proximal and distal barriers.


An exemplary expandable structure 26 is formed by cutting slots in a superelastic alloy tube such as a nickel titanium alloy or Nitinol™ tube. As can be understood with reference to FIG. 6B, expandable structures 54 may have circumferential widths 80 which are enhanced adjacent an electrode and/or electrode mounting location 82. As can be seen in FIG. 6A, the localized enhancement of the width 80 adjacent electrode mounting pads 82 may be axially offset, as described above. The slots forming expandable members 54, and hence the expandable members themselves may, for example, be 0.8 inches in length, with the expandable members having a circumferential width of about 0.25 inches.


Referring now to FIGS. 7A and 7B, side and end views of an expandable barrier in the form of a collapsible cone can be seen. Barrier 66 here comprises a braided Nitinol™ wire 84 coated in silicone, for example, by dipping a braid of a superelastic alloy such as a Nitinol™ braid in liquid silicone and allowing it to harden. Such cones may then be mounted over the proximal and distal portions of the expandable structure. As noted above, a variety of alternative barrier membranes may be employed. FIG. 7C illustrates a basket 75 with an integral barrier 77 coated directly on the basket. Barrier 77 comprises a polyurethane, which may be quite tear resistant. Alternative barrier membranes may comprise other materials such as PTFE or the like.


Referring now to FIGS. 8 and 9, exemplary electrodes 50 supported by polyimide alloy expandable members 54 may be coated with a high-temperature polymer. Conductors 52 extend proximally from electrodes 50 as described above. High contrast radiopaque markers such as gold, platinum, platinum/iridium alloy, and the like may be attached to or near these struts. The markers could also be used as the electrodes.


The use of catheter system 10 for remodeling and/or removal of eccentric atheroma from within a blood vessel can be understood with reference to FIGS. 10A through 10E. As seen in FIG. 10A, accessing of a treatment site will often involve advancing a guidewire GW within a blood vessel V at, and more often distally beyond a target region of atherosclerotic material AM. A wide variety of guidewires may be used. For accessing a vessel having a total occlusion, guidewire GW may comprise any commercially available guidewire suitable for crossing such a total occlusion, including the Safe-Cross™ RF system guidewire having forward-looking optical coherence reflectrometry and RF ablation. Where atherosclerotic material AM does not result in total occlusion of the lumen, such capabilities need not be provided in guidewire GW, although other advantageous features may be provided. For example, guidewire GW may include a distal balloon to hold the guidewire in place and further inhibit movement of ablation debris and the like. Guidewire GW may be positioned under fluoroscopic (or other) imaging.


Catheter 12 is advanced distally over guidewire GW and positioned adjacent to atherosclerotic material AM, often toward a distal portion of the occlusion as can be understood with reference to FIGS. 10A and 10B. Expandable structure 26 expands radially within the lumen of the blood vessel so that electrodes 50 radially engage atherosclerotic material AM. Expandable structure 26 may be expanded by, for example, pulling a pullwire extending through catheter body 14 to the coupled (directly or indirectly) to distal portion 62 of expandable body 26 (see FIG. 3). Alternatively, an inner catheter body 58 may be moved proximally relative to outer catheter body 14, with the inner catheter again being coupled to the distal portion of the expandable body. Still further alternatives are possible, including withdrawing a sheath from around the expandable body and allowing the expandable body to flex radially outwardly. In at least some embodiments, whether actuated from the proximal end of catheter 12 or simply by releasing the expandable body, the structural members defining the expandable body may comprise elastic or superelastic materials treated to expand radially outwardly, such as by heat-setting a superelastic Nitinol™ metal, polyimide, or the like. In some embodiments, guidewire GW may be removed after the ablation catheter is positioned and/or the basket is expanded. As atherosclerotic material AM is distributed eccentrically about catheter 12, some of electrodes 50 directly engage a luminal wall W, as can be understood with reference to FIGS. 10B and 10C.


Imaging catheter 34 is positioned within a lumen of catheter 12 so that detector 42 extends to adjacent atherosclerotic material AM. The imaging catheter operates within and/or through catheter 12 so as to measure a thickness of atherosclerotic material concentrically about catheter 12 as illustrated in FIG. 10C with measurements often being taken at a plurality of axial locations so as to measure axial variation of the atherosclerotic material AM within the blood vessel, such measurements often progressing proximally. In many cases, atherosclerotic material AM will be distributed eccentrically within the vessel wall as shown in FIG. 10C. It should be noted that no portion of the vessel wall need be completely uncovered by atherosclerotic material for the measurement distribution to indicate that the obstruction is eccentric, as a relatively thin layer of atheroma along one portion or side of the blood vessel may be much different in thickness than a very thick layer of atherosclerotic material on an opposite side of the blood vessel V. In some methods, remodeling and/or ablation of all atheroma along one side may result in electrode/vessel wall engagement only after treatment begins.


In some cases, imaging catheter 34 may allow identification and/or characterization of atherosclerotic materials, plaques, tissues, lesions, and the like from within a blood vessel. For example, imaging catheter 34 may determine an axial and/or circumferential localization of a target plaque for treatment. Where treatments are intended for atherosclerotic plaques so as to enhance blood flow through the lumen, the treatment may be tailored to provide short term and/or long term increases in lumen diameter and blood flow. Where catheter 34 identifies a circumferentially and/or axially localized vulnerable plaque, that vulnerable plaque may be targeted for a suitable treatment to inhibit deleterious release of thrombolitic materials, often by thickening a fibrous cap of the vulnerable plaque, making the plaque less vulnerable to rupture, decreasing a size or danger of release from a lipid-rich pool of the vulnerable plaque, or the like. Hence, catheter 34 may be used to provide information similar to that available through histology so as to indicate a composition of an atheroma (by identifying and location, for example, a fibrous cap, smooth muscle cells, a lipid pool, calcifications, and the like.) Intravascular ultrasound catheters may now be capable of such atheroma characterizations, and these characterizations may also be provided by optical coherence tomography intravascular catheters, intravascular MRI antennas, and other catheter-based imaging systems, or by non-invasive imaging modalities such as MRI systems, and the like.


Suitable imaging catheters for use in the present catheter system are commercially available from a wide variety of manufacturers. Suitable technology and/or catheters may, for example, be commercially available from SciMed Life Systems and Jomed-Volcano Therapeutics (providers of intravascular ultrasound catheters), Light Lab™ Imaging (developing and commercializing optical coherence tomography catheters for intravascular imaging), Medtronic CardioRhythm, and the like. Still further alternative technologies may be used, including ultra fast magnetic resonance imaging (MRI), electrical impedance atheroma depth measurements, optical coherence reflectrometry, and the like.


The systems, devices, and methods described herein may optionally make use of imaging techniques and/or atherosclerotic material detector devices which are at least in part (optionally being entirely) disposed outside of the body lumen, optionally being disposed outside of the patient body. Non-invasive imaging modalities which may be employed include X-ray or fluoroscopy systems, MRI systems, external ultrasound transducers, and the like. Optionally, external and/or intravascular atherosclerotic material detectors may also be used to provide temperature information. For example, a system having an MRI antenna may detect tissue temperatures such that a graphical indication of treatment penetration may be presented on the system display. Tissue temperature information may also be available from ultrasound and/or optical coherence tomography systems, and the temperature information may be used as feedback for directing ongoing treatments, for selecting tissues for treatment (for example, by identifying a hot or vulnerable plaque), and the like.


As with positioning of guidewire GW and advancement of catheter 12, positioning of sensor 30 of imaging catheter 34 may be facilitated by fluoroscopic or other imaging modalities. Location of sensor 36 relative to expandable structure 26 may be facilitated by radiopaque markers of catheter 34 adjacent sensor 36, and by the radiopaque structure (or corresponding radiopaque markers placed on or near) expandable structure 26, and/or by the use of radiopaque electrodes.


By expanding expandable structure 26 within blood vessel V, optional proximal and distal barriers 66, 68 (see FIG. 3) may form an at least partially, and preferably a substantially isolated environment within the blood vessel. That environment may be adapted to improve subsequent remodeling and/or ablation by aspirating blood from a port of aspiration lumen 22 disposed between proximal and distal barriers 66, 68, and by irrigating the isolated environment with a desired fluid, as described above. When provided, aspiration and/or irrigation may be performed, optionally simultaneously, so as to generate a flow within the controlled environment for removal of any vaporization gases, ablation debris, and the like.


Referring now to FIGS. 10C and 10D, circumferential imaging often indicates that remodeling and/or ablation should be targeted to an eccentric portion or region R of the vessel wall W. To aid in registering the electrodes with the circumferential atheroma distribution, one strut of expandable structure 26 has an identifiable image, allowing the strut to serve as a rotational alignment key. Registering the electrodes may be achieved using intravascular imaging such as intravascular ultrasound (IVUS), optical coherence tomography (“OCT”), intravascular MRI, and/or the like, optionally using external imaging such as fluoroscopy, magnetic resonance imaging (“MRI”), or the like. Electronic registration may also be used. In response to this information, RF energy is directed to electrodes within region R. These actively energized electrodes define a subset of the overall array of electrodes, and selection of this subset of electrodes may be implemented using a controller as described hereinbelow.


The mechanisms of ablating atherosclerotic material within a blood vessel have been well described, including by Slager et al. in an article entitled, “Vaporization of Atherosclerotic Plaque by Spark Erosion” in J. of Amer. Cardiol. (June, 1985), on pp. 1382-6; and by Stephen M. Fry in “Thermal and Disruptive Angioplasty: a Physician's Guide;” Strategic Business Development, Inc., (1990) the full disclosures of which are incorporated herein by reference. Suitable vaporization methods and devices for adaptation and/or use in the present system may also be described in U.S. Pat. Nos. 5,098,431; 5,749,914; 5,454,809; 4,682,596; and 6,582,423, among other references. The full disclosure of each of these references is incorporated herein by reference.


As illustrated in FIG. 10, energizing of selected electrodes 50 may result in vaporization of atherosclerotic material AM, so that the atherosclerotic material is removed from the blood vessel with an aspiration flow F through a lumen of catheter 12. A concurrent irrigation flow helps maintain the environment between the proximal and distal barriers of the catheter, and these two flows allow gases G and ablation debris to be entrained while inhibiting release of such emboli within blood vessel V. The fluid may also act as a cooling fluid to limit heating and collateral damage to other tissues, the circulating fluid often being at least less than body temperature, optionally being at or below room temperature.


Referring now to FIG. 10E, as described above, it may not be necessary to completely remove all atheroma or atherosclerotic material from within the blood vessel. Providing an open lumen having an effective diameter of at least 80 or 85% of a nominal native lumen diameter may be sufficient. Remodeling treatments may provide acute effective open diameters in a range from about 30% to about 50%. In some embodiments, injury caused to the atherosclerotic material with the energized electrodes or other energy directing surfaces may result in subsequent resorption of the injured tissue lesions so as to provide further opening of the vessel after termination of treatment as part of the healing process.


To promote long term efficacy and inhibit restenosis of a treated region of blood vessel V, a restenosis inhibiting catheter 40 may be advanced through a lumen of catheter 12, so that a radiation source 42 irradiates the treated region of the blood vessel. Suitable intravascular radiation catheters are commercially available from Novoste™, Guidant, Johnson & Johnson, and the like. Restenosis inhibiting drugs similar to those now being employed on drug eluting stents may also be advanced through a lumen of catheter 12, optionally while the proximal and distal barriers again help to maintain a controlled environmental zone within the blood vessel, so that systemic drug delivery might be limited or avoided. In addition to known restenosis inhibiting drugs used on drug eluting stents, drugs which cause vasodilation might be employed. Known restenosis inhibiting drugs such as Rapamycin™ may also be used.


In some embodiments, expandable structure 26 may remain expanded against the vessel wall W and/or atherosclerotic material AM while catheter 12 moves within the blood vessel, the catheter often being drawn proximally during or between ablation treatments. Analogous movement of a radially expanded perforate basket is employed, for example, when measuring temperatures of blood vessels so as to detect vulnerable plaque in systems now being developed and/or commercialized by Volcano Therapeutics. Alternatively, the basket may be repeatedly contracted, axial movement of the catheter 12 employed to reposition the basket, with subsequent expansion of the basket at each of a plurality of treatment locations along atherosclerotic material AM. Repeated intravascular imaging or other atherosclerotic material thickness measurements circumferentially about catheter 12 may be employed, with the remodeling and/or ablation often being halted temporarily so as to allow an image to be acquired intermittently during an ablation procedure. A final image may be taken to verify remodeling and/or ablation has been successful.


Referring now to FIGS. 11 through 21, a variety of alternative catheter structures are schematically illustrated, with many of these structures providing a microenvironment or controlled environmental zone within the blood vessel which has been enhanced for remodeling and/or ablation. A variety of emboli inhibiting barriers are also described and/or illustrated, including silastic balloons, flexible lips, or expandable cones which may be axially offset from the ablation electrodes. For example, referring to FIGS. 11 and 12, a system similar to that illustrated in FIG. 2 may employ a remodeling and/or ablation sleeve 102 having a proximal hub 104 and receiving an imaging catheter and a guidewire GW in an axial lumen of the sheath. A microenvironment is provided by a microchamber lip 106, which may comprise silicon or the like. Bipolar electrodes 50 may (though need not necessarily) generate gas and/or other ablation debris, which the silicon lip may help to contain. A vacuum port 108 of hub 104 is in fluid communication with a vacuum port 110, while a saline fluid infusion port 112 together with a saline injection passage 114 may be used to control and/or modify the microenvironment for remodeling and/or ablation. As illustrated in FIG. 13, alternate microchambers may be effected using silicon-like lips 116 fully encircling the catheter sheath 102, dual balloons, or the like. As illustrated in FIG. 14, such structures may be combined with a basket 118 supporting RF electrodes so as to provide electrode contact within a microchamber. The basket may optionally comprise a Nitinol™ shaped memory alloy.


Referring now to FIG. 15, more generally, remodeling/ablation sleeve 102 may support electrode 50 for radiofrequency energy, and may provide one or more lumens for coaxial and/or biaxial insertion of an imaging catheter 34 (such as an IVUS catheter) and/or guidewire GW. Imaging catheter 34 may have a transducer in the form of an array 120.


Referring now to FIG. 16, a remodeling/ablation sleeve 102 similar to that shown in FIGS. 11 and 12 has (here in cross section) has an electrode wire lumen 122, a saline injection lumen 124, and the opening of the vacuum port 110 to the working lumen of sheath 102 in which the imaging or IVUS catheter 34 and guidewire GW are disposed. A silicon lip or valve 126 allows a vacuum to be transferred to the microenvironment.


Still further alternative arrangements are illustrated in FIGS. 17 and 17A. In the embodiment of FIG. 17, an inner electrode 128 is used in a bipolar system along with outer electrodes 50, which contact the tissue for treatment. FIG. 17A schematically illustrates use of a balloon catheter 130 having a balloon 132 (such as a latex balloon). On the surface of the latex balloon electrodes 50 are mounted for use in selected pairs. Hence, a balloon (rather than a basket structure) may be used as a radially expandable structure for carrying the electrodes or other energy delivery surfaces.



FIG. 18 schematically illustrates an expandable basket 134 being contracted from a large configuration to a small configuration. The basket may optionally be used as a cutting basket by providing appropriate edges, and/or may capture emboli within. FIG. 19 illustrates a remodeling/ablation sleeve 102 in which imaging catheter 34 travels axially back and forth to image, and in which a silastic balloon 135 is disposed distal of the treatment debris for emboli capture. FIG. 20 illustrates an alternate electrode delivery balloon 138 similar to balloon 132 of FIG. 17A, and illustrates electrodes 50 having flexible lumen extensions extending proximally therefrom. FIG. 21 schematically illustrates an RF electrode within a microchamber provided by proximal and distal barriers 140, 142 of sheath 102, in which a position of electrode 50 is actuated in the microchamber.


Referring now to FIGS. 22 and 23, alternative controllers 92a, 92b selectively energize electrodes of catheter 12 with RF power supplied from an RF generator 94. A wide range of RF energy types may be employed, including burst of 500 Khz, different types of waveforms, and the like. In controller 92a, a simple dial 96 is turned to point to a desired electrode pair to be energized. A “key” electrode may be registered with the intravascular imaging system, either electronically or by providing an electrode, electrode support member, or attached marker which presents a distinct image on the intravascular imaging display. This simplifies selection of one or more eccentric electrode pair along atheroma. Advantageously, catheter 12 need not be rotated into a proper orientation to accurately remodel and/or ablate the desired eccentric atherosclerotic material. Controller 92b includes similar capabilities, but allows the operator to select multiple electrodes for driving bipolar RF energy therebetween, providing greater flexibility in allowing multiple electrodes to be simultaneously energized. FIGS. 23 and 24 illustrate monopoly control arrangements similar to those of FIGS. 21 and 22, respectively. Patient grounding may be effected by a patient grounding plate, a ring electrode 2 to 5 cm proximal to basket 26, or the like. Once again, no catheter rotation is required to orient an active side of the catheter adjacent to the targeted atheroma since various eccentric ablation orientations can be selected through the electrode selection controller.



FIGS. 26 and 27 schematically illustrate alternative fluid flow arrangements for use in the catheters and methods described herein. In the embodiment of FIG. 26, a tubular body 150 extending proximally from expandable body 26 includes one or more irrigation ports 152, the irrigation ports here being disposed proximally of the expandable body. An aspiration port 154 contains a tubular body defining a guidewire and/or imaging catheter lumen 156. Irrigation fluid may flow distally, which may also be the direction of blood flow in the body lumen. Irrigation fluid may be aspirated through the aspiration port. In the embodiment of FIG. 27, lumen 154 is used for aspiration and for a guidewire and/or imaging catheter.


An alternative controller is illustrated in FIGS. 28A-D. This controller allows an operator to choose, for each electrode, whether to keep that electrode inactive, electrically couple that electrode to a first pole (sometimes referred to as pole A) of an energy source (such as an RF generator or the like), or to electrically couple that electrode to a second pole or pole B of the energy source. This controller allows a wide range of energized electrode configurations, including pseudo-monopolar modes where all electrodes except one are connected to one pole of the energy source (pole A) and one electrode is connected to the other pole (pole B). As can be understood with reference to FIG. 28A, controller 160 allows testing of many electrode configurations for RF remodeling and/or ablation, particularly those involving two or more electrodes. A switch panel 162 is shown in more detail in FIG. 28B. Each electrode (in this embodiment, up to eight electrodes) is electrically coupled to a 3-way switch numbered from 1 to 8, a switch disposed in the middle position indicates the electrode is not coupled to either pole, while a switch pushed toward the plus sign indicates the associated electrode is coupled to a red RF connector with the controller. Similarly, a switch pushed toward the minus sign indicates the associated electrode is electrically coupled to a black RF connector of the control box.


As can be understood with reference to 28C, electrodes associates with switches 3-8 are not coupled to either pole, electrode 1 is connected to the red RF connector, and electrode 2 is connected to the black RF connector. Activation of the RF generator will circulate bipolar RF energy between electrodes 1 and 2. In FIG. 28D, electrodes 5-8 are not energized, while electrodes 1 and 3 are coupled to the red RF connector. Electrodes 2 and 4 are connected to the black RF connector, so that activation of the RF generator will circulate bipolar RF energy between electrodes 1 and 3 and between electrodes 2 and 4.


An exemplary self-expandable basket is illustrated in FIGS. 29A-29H. As can be understood from these drawings, electrodes may be fabricated as part of the struts 172 from which the basket is formed, for example, using a radially outwardly oriented surface of a localized widening 174 of each strut disposed in axially central portion of the strut, as can be seen in FIGS. 29B and 29E. Each arm may be formed from one piece of material, optionally comprising a Nitinol™ nickel-titanium shaped memory alloy, with the struts optionally being laser cut from a Nitinol™ tube. The electrode/basket may be, for example, coated with a high temperature polymer such as a polyimide. Electrodes 174 may be formed by inhibiting coating or removing coating from the desired portion of the associated strut 172 (as illustrated in FIG. 29E) so that the electrode surface is exposed for contact with atherosclerotic material. The struts may be separated from each other and structurally supported with an insulated material such as ultraviolet (“UV”) cure or heat shrink sleeve, a polyethylene, Nylon™, or the like to form basket 170.


Each strut 172 may be used to conduct energy between electrode surface 174 and an electrical conductor extending proximally from the strut toward a controller. Proximal pads for connecting such conductors are illustrated in FIG. 29C, while distal structural pads 178 are illustrated in FIG. 29D. Adjacent electrodes 174 may be axially offset or staggered as can be seen in FIG. 29F. Insulating coating along each strut 172 may be inhibited or removed from an inner surface of proximal pads 176 so as to facilitate connecting of an associated conductive wire, such as by spot welding or the like. Alternative insulating materials may also be used, including parylene coatings, while alternative methods for attaching struts 172 to a catheter body may be employed, including adhesive bonding using insulating UV cure, embedding the pad structures in polyethylene, and the like.


Exemplary structures for fixing struts 172 of basket 170 to a catheter body 180 are illustrated in FIG. 29G.


Referring now to FIGS. 29F and 29H, an alternative indicia providing a distinguishable image for rotationally registering selected electrodes 174 of basket 170 to images or other atherosclerotic material measurements can be understood. In this embodiment, an electrode 174i referenced as electrode 1 may have a radiopaque marker 182 disposed on the associated strut 172i. A strut 172ii supporting an associated second electrode 174ii may have two radiopaque markers 182 provide a circumferentially asymmetric count indicator allowing all electrodes to be referenced without ambiguity. The shape of electrodes 50 may vary, for example, electrodes 174 may be wider than other portions of struts 172 as illustrated in FIGS. 29A-G.


As described above, remodeling will often be performed using irrigation and/or aspiration flows. In many embodiments, an irrigation port directs fluid, such as a saline solution, from an irrigation lumen to an interior of the basket. An aspiration port may provide fluid communication between an aspiration lumen and an interior of the basket. One or both of these fluid flows may be driven continuously, or may alternatively pulsate before, during, and/or after treatment. In some embodiments, aspiration and/or irrigation flow may occur acutely or concurrently so as to circulate between the irrigation port and the aspiration port. Optionally, the flow may carry ablation debris to the aspiration port, where the debris may be evacuated through the aspiration lumen. There may be coordination between the irrigation system and the aspiration system such that the irrigation fluid may remain confined in an area closely adjacent the basket so as to inhibit embolization of ablation debris when the basket is expanded within the blood vessel. Such coordination, for example, may inhibit distal movement of ablation debris, and/or may obviate any need for a distal and/or proximal barrier or membrane. In some embodiments, the circulation of fluid between an irrigation port and an aspiration port may create an effectively bloodless environment adjacent the electrodes to facilitate remodeling and/or ablation, imaging of atherosclerotic tissue, and the like.


Referring now to FIGS. 30A and 30B, control of energy directed from the catheter systems and structures of the present invention may optionally make use of thermocouples and other temperature sensing structures. Thermocouples such as K-type thermocouples (+CH/−AL) may be attached to or near one or more struts of an expandable structure to provide temperature measurements. For example, such structures may provide tissue temperature measurements, blood temperature measurements, treatment temperature measurements, and/or the like.


Optionally, a temperature measurement structure may also be used as an RF electrode, for example, by employing one or more of the structures illustrated in FIGS. 30A and 30B. In the embodiment of FIG. 30A, a thermocouple 182 can be coupled to either an RF energy source 184 or a thermometer 186 by a switch 188. A similar embodiment is illustrated in FIG. 30B.


Referring now to FIG. 31, an alternative catheter system 190 includes a plurality of electrodes 50 supported by struts 192. Struts 192 expand radially when extended distally through a sheath 194 so that a circumferential array of the electrodes is collapsible. A ball-shaped tip 196 includes proximally oriented high pressure jets 198, and the ball-shaped tip may be used as one pole with selected electrodes 50 being used as the other pole. Alternatively, bipolar power may be driven between electrodes 50 or the like. Optionally, a proximal barrier 200 such as a screen may be used to inhibit movement and/or capture any debris.


When the RF electrodes are energized, the high pressure jets may also be activated so as to provide a saline flush. A venturi effect may entrain the debris for transport proximally through a catheter lumen for evacuation, typically using an aspiration source coupled to sheath 194. Debris may be trapped in barrier 200 which may comprise a screen, a solid sheet, a net, or the like. In some embodiments, low pressure jets may be used from adjacent ball tip 196 in place of high pressure jets.


Referring now to FIGS. 32A-32D, alternative expandable structures may avoid kinking or flattening of the expandable structure when the expandable structure bends axially, such as when it is expanded along a bend in a body lumen. In the embodiment of FIG. 32C, a coil or helical expandable structure 202 has a small profile configuration 204 and a large profile configuration 206, and may be deployed and/or retracted by twisting a distal end 208 and/or a proximal tubular body 210 relative to each other, by a pull/release mechanism, or the like. Aspiration and/or irrigation may be provided through the proximal tubular member 210 as described above, and the coil structure may include a single loop or a plurality of loops so as to provide one or more circumferential rows of electrodes 50 when in the expanded configuration 206. In the embodiment of FIG. 32D, an inflatable expandable structure 212 includes axial struts and/or rings formed as tubular inflatable balloons so as to allow the expandable structure to expand from the small profile configuration to the shown large-profile configuration.


Still further alternative expandable structures and energy delivery surfaces are schematically illustrate in FIGS. 33-35. In a microwave treatment device 216 illustrated in FIG. 33, each strut of a basket may include a helicoidal microwave antenna, with an inner side of the antenna shielded to avoid emitting energy toward the catheter axis. Alternative microwave antennas may also be employed, including unidirectional antennas which allow depth between an energy delivery surface and a target tissue to be varied by varying a focus of the antenna. Such focused microwave devices may include antennas that are rotatable about the catheter axis, axially moveable, and the like.


In the embodiments of FIGS. 34 and 35, catheter bodies again support a series of struts 218, 220 and also have a plurality of irrigation or flush lumens. The irrigation lumens within the catheter body are in fluid communication with tubular structures extending along the (and in some cases being integrated into the) struts, so that fluid flush ports 222 direct saline or other fluids towards electrodes 50 or microwave antennas 224. Electrosurgical power for the energy delivery surfaces may be transmitted using the strut structure, or wires 226 may extend along the strut to the energy delivery surfaces. In the embodiment of FIG. 35, shield 228 along an inner portion of a microwave antenna 224 can be seen, which may limit microwave energy directed toward an imaging catheter. For embodiments employing microwave antennas as energy delivery devices, only one antenna of the circumferential array may be energized at a time, so as to avoid interference between conductors along the catheter body.


Referring now to FIG. 36, controllers of the catheter systems described herein may allow distribution of differing power levels to differing pairs of electrodes. For example, in response to a circumferential distribution of atherosclerotic material AM such as that illustrated in FIG. 36, a controller may direct 50 watts of energy to a first electrode 230, 30 watts of energy to a pair of second electrodes 232 and only 10 watts of energy to a pair of third electrodes 234. Other electrodes may have no energy directed thereto, as described above. In some embodiments, a differing power directed to the differing electrodes may be provided by controlling the duty cycle, for example, with 50 watts being provided by energizing one or more electrode for 50% of the time, 30 watts being provided by energizing an electrode 30% of the time, and the like.


Referring now to FIGS. 37A-37C, many imaging modalities (including intravascular ultrasound, optical coherence tomography, intravascular MRI, and the like) may be at least in part blocked or degraded by positioning the image detecting structure within a metallic structure such as a basket formed of Nitinol™. Hence, there may be advantages in producing alternative expandable structures such as baskets comprising plastics or a polymer. In light of the heat generated by the electrodes of the systems described herein, it may be advantageous for such polymer basket structures 240 to comprise a high temperature polymer such as a polyimide. Alternative basket structures may comprise HDPE, PET, Nylon™, PEBAX™, and the like. As illustrated in FIG. 37B, proximal ends of the basket struts may be glued to a shaft 242 at a bond 244. An imaging catheter guide 246 may extend through a distal end of the basket structure 248, with the distal end of the basket free to slide axially along the guide. Pullwires 250 may be affixed to the distal end 248, so that pulling of the pullwires radially expands basket 240, with the pullwires running inside the proximal shaft 242. The basket may be retracted back to its small profile configuration by pushing of the pullwires, or the basket may include biasing means urging the basket to the small profile configuration. So as to avoid degradation to imaging performance, polymer tension members similar to fishing line may be used as pullwires. In the exemplary embodiment, the pole wires comprise Nitinol™ which has sufficient compressional rigidity to push the basket to its small profile configuration.


Basket 240 may be formed by cutting struts from a tube of the polymer material, with the distal portion 248 preferably remaining uncut. The proximal ends of the struts may be separated prior to forming bond 244, and ring-shaped RF electrodes may be slid along each arm and glued to the desired configuration along the intermediate portion of the basket.


Exemplary treatment methods are illustrated in FIGS. 38A-38H. In FIG. 38A, the catheter system 260 includes a basket covering sheath 262 over an atherosclerotic material detecting and treating catheter 264 as described above. In this embodiment, outer basket sheath 262 radially restrains the basket 266, which is biased to expand radially when released from the outer sheath, as illustrated in FIG. 38B. In some embodiments, the basket may be expanded after the outer sleeve is retracted, such as by pulling pullwires, rotating one portion of the catheter relative to the other, or the like. Regardless, as the basket expands within the vessel V, electrodes 50 of the basket engage the surrounding vessel wall. An imaging transducer near basket 266 of an imaging catheter disposed in a lumen of the treatment catheter evaluates the vessel V, and the detection/treatment catheter system 264 is pulled proximally along the artery or vessel V.


When the imaging catheter detects atherosclerotic material AM as illustrated in FIG. 38C, an appropriate subset (possibly including only a single electrode 50) is activated to remodel the atherosclerotic material AM, as illustrated in FIG. 38D, and the open vessel lumen size increases moderately during treatment. The catheter is pulled proximally to the next atheroma, which is again detected and treated. A cross section of the limited open lumen prior to treatment is schematically illustrated in FIG. 38F, which also illustrates a saline flush or irrigation lumen 268 of the catheter 264. Treatment energy and the moderate increase in the open lumen diameter of the vessel V are schematically illustrated in the cross section of FIG. 38G. After a healing response gradually increases the open lumen diameter, the longer term open lumen results schematically illustrated in FIG. 38H may then be provided.


Referring now to FIGS. 38A and B, eccentric material removal in a gelatin artery model 270 are presented. Prior to the test, the artery model includes a consistent lumen 272 as seen in FIG. 38A. A test eccentric treatment catheter 274 having an expandable basket supporting a circumferential array of electrodes is introduced into lumen 272, with the expandable basket supporting the electrodes in engagement with the luminal wall. Selected electrodes of test catheter 274 were energized so as to eccentrically treat the gelatin artery model 274, thereby effecting eccentric remodeling of the gelatin model, in this case by removing an eccentric volume 276 from along one side of lumen 272. The orientation and amount of the material removed was controlled by selectively energizing electrodes of test catheter 274.


Referring now to FIG. 40, an exemplary catheter system 280 is illustrated. In this embodiment, catheter body 282 includes only a single lumen, which is large enough to accommodate an imaging catheter therein and also to be used as an irrigation lumen to bring irrigation fluid to irrigation ports 284. The lumen may decrease in diameter distally of irrigation ports 284, with the decreased diameter portion 286 fittingly receiving the imaging catheter within the lumen thereof so as to direct the irrigation fluid radially outward through the plurality of irrigation ports. This embodiment may be particularly useful when remodeling atherosclerotic materials using the methods illustrated in FIGS. 38A-38H, in which mild heating improves vessel size without requiring aspiration.


Catheter body 282 may include a braided shaft in which conductive wires (for example copper wires or beryllium-copper wires) are coated with a high temperature and/or high strength insulation material such as a layer of polyimide or the like. The braided wires may be sandwiched between layers of materials forming the shaft of catheter body 282. The shaft may, for example, comprise a plurality of layers of polyethylene, an inner Teflon™ PTFE layer, an outer nylon layer, and the like.


The wires of shaft 282 may be braided so as to inhibit capacitive losses between wires when electrical currents run through them. Capacitive losses may be decreased when a wire that carries a current from an energy source to an electrode of the catheter system and a wire that carries a current from an electrode back to the energy source are not parallel, but at an angle, ideally being perpendicular. This may be achieved by braiding the wires with appropriate pitch or a number of peaks per inch. The basket structure 170 of catheter system 280 may be included, with the basket structure being described in more detail with reference to FIGS. 29A-29H. Guide 286 may extend through basket 170 and may comprise a material transparent to the imaging catheter, optionally comprising HDPE, PET, or the like.


Still further alternatives are available. For example, another way to employ RF energy to remodel atherosclerotic material may be to energize a plurality of the adjacent electrodes with differing RF signals so as to employ the adjacent electrodes as a phase-array. A phase array can direct or steer an electromagnetic signal in a desired direction using constructive and destructive interferences between signals of adjacent elements of the array. By controlling phases of the adjacent signals, a phase array of electrodes may provide a focused and/or steerable RF signal.


Along with controlling steering and directionality, adjusting phases of adjacent RF electrodes may allow focusing of some or most of the RF energy at a desired depth D inside the atherosclerotic material while inhibiting RF energy delivery between the electrode surfaces and depth D using constructive and destructive interference between the signals. For example, such a system may be employed to preserve the cap of a plaque so as to reduce restenosis. Inhibiting heating of the cap while focusing energy toward an internal portion of the plaque may lower an immune response to heat that could otherwise lead to restenosis. Hence, inhibiting heating of the cap may reduce restenosis.


In general, the present invention may use of highly elastic, expandable structures, particularly of expandable structures formed from structural members separated by perforations so as to define a “basket.” Such structures can conform to an artery diameter before, during, and/or after atherosclerotic material removal. This expandability allows for direct contact of the electrodes against atheroma, although the systems of the present invention may also make use of conductive fluid environments to complete an RF energy path, or conversely, use non-conductive fluid to enhance energy directed through tissue. Multiple electrodes can be distributed circumferentially around an intermediate portion of the expandable structure, and a subset of these electrodes can be activated to allow for eccentric tissue remodeling and/or ablation.


Atheroma may be identified and targeted by intravascular imaging, and these capabilities may be integrated into the remodeling and/or ablation catheter. Preferably, the intravascular imaging capabilities will be deployed in a separate catheter which can be advanced within, and removed from the ablation catheter. In general, this intravascular imaging capability allows the progress of the therapy to be monitored so that wall perforation can be avoided, while ideally reducing occlusion to no more than 15% of the overall native vessel diameter (either upon completion of the treatment or after subsequent tissue healing). The ablation catheter may further allow the use of localized radiation or drug delivery for antirestenosis treatments. The ablation catheter may include a relatively large lumen allowing selective use of an intravascular imaging system, a radiation delivery or other treatment catheter, an aspiration of debris and vaporization gases, with these uses often being employed sequentially. A guidewire may make use of this or a separate lumen, and the guidewire may be removed to allow access for the restenosis and/or imaging catheters.


While the exemplary embodiments have been described in some detail, by way of example and for clarity of understanding, those of skill in the art will recognize that a variety of modification, adaptations, and changes may be employed. Hence, the scope of the present invention should be limited solely by the appending claims.

Claims
  • 1. A system for remodeling tissue about a body lumen, the system comprising: (a) an energy source;(b) a catheter coupled to the energy source, the catheter including an expandable device comprising a plurality of electrodes sequentially positioned along a length of the expandable device in a helical pattern, wherein the expandable device is configurable between an expanded condition and an unexpanded condition, wherein when in the unexpanded condition, at least some of the plurality of electrodes are longitudinally and circumferentially offset relative to adjacent electrodes, wherein the expandable device moves from the unexpanded condition to the expanded condition upon activation of a release mechanism, wherein the system is configured to remodel a target tissue while inhibiting damage to collateral tissue; and(c) a controller configured to selectively energize a subset of the plurality of electrodes.
  • 2. The system of claim 1, wherein, when the expandable device is in the expanded condition, the plurality of electrodes are in the helical pattern.
  • 3. The system of claim 2, wherein the plurality of electrodes are positioned along an elongated body.
  • 4. The system of claim 3, wherein the elongated body includes at least one helical loop when the expandable device is in the expanded condition.
  • 5. The system of claim 4, wherein the elongated body includes a plurality of helical loops when the expandable device is in the expanded condition.
  • 6. The system of claim 4, wherein the elongated body is substantially straight when the expandable device is in the unexpanded condition.
  • 7. The system of claim 3, wherein the elongated body includes a nickel and titanium alloy.
  • 8. The system of claim 1, wherein at least some of the electrodes are separated from adjacent electrodes by an insulative material.
  • 9. The system of claim 1, wherein the electrodes comprise bipolar or monopolar electrodes.
  • 10. The system of claim 1, further comprising at least one temperature sensor associated with the expandable device.
  • 11. The system of claim 1, further comprising at least one irrigation lumen associated with the expandable device.
  • 12. The system of claim 1, wherein the expandable device is associated with a catheter proximate a distal end of the catheter.
  • 13. A system for remodeling tissue about a body lumen, the system comprising: (a) an energy source;(b) a catheter coupled to the energy source, the catheter including an expandable device comprising a plurality of electrodes sequentially arranged along the expandable device and longitudinally and circumferentially spaced relative to adjacent electrodes, wherein the plurality of electrodes are arranged along an elongated body, wherein the elongated body is configurable between an unexpanded configuration in which the plurality of electrodes are axially and circumferentially offset from adjacent electrodes and an expanded configuration in which the elongated body is a helical shape, wherein the elongated body moves from the unexpanded configuration to the expanded configuration upon activation of a release mechanism, wherein the system is configured to remodel a target tissue while inhibiting damage to collateral tissue; and(c) a controller configured to selectively energize a subset of the plurality of electrodes.
  • 14. The system of claim 13, wherein the helical shape includes a plurality of helical coils.
  • 15. The system of claim 14, wherein the plurality of helical coils are sequentially arranged along the expandable device.
  • 16. The system of claim 13, wherein the elongated body is a tube including at least one irrigation lumen.
  • 17. The system of claim 13, wherein at least some of the plurality of sequentially spaced electrodes are separated from adjacent electrodes by an insulative material.
  • 18. A system for remodeling tissue about a body lumen, the system comprising: (a) an energy source;(b) a catheter coupled to the energy source, the catheter including an expandable device, comprising an elongated body associated with a distal portion of an elongated catheter, the elongated body including a plurality of electrodes sequentially positioned along the elongated body, wherein the elongated body is moveable between an expanded configuration and an un-expanded configuration, wherein, when in the expanded configuration, the elongated body is helical and includes at least one loop, wherein the elongated body moves from the un-expanded configuration to the expanded configuration upon activation of a release mechanism, and wherein, when in the un-expanded configuration, the elongated body is substantially straight and the plurality of electrodes are circumferentially spaced relative to adjacent electrodes; and(c) a controller configured to selectively energize a subset of the plurality of electrodes.
  • 19. The system of claim 18, wherein, when in the expanded configuration, the elongated body includes a plurality of loops.
  • 20. The system of claim 18, wherein the elongated body is a tube including at least one irrigation lumen.
  • 21. The system of claim 18, wherein the elongated body is at least partially formed from a nickel and titanium alloy.
  • 22. A system for remodeling tissue about a body lumen, the system comprising: (a) an energy source;(b) an expandable device associated with an elongated catheter coupled to the energy source, wherein the expandable device moves from an un-expanded configuration to an expanded configuration upon activation of a release mechanism, wherein the expandable device, when in an expanded configuration, includes at least one helical loop, wherein the helical loop includes a plurality of electrodes sequentially spaced along the helical loop and circumferentially spaced relative to adjacent electrodes, and wherein, when in the un-expanded configuration, at least some of the plurality of electrodes are circumferentially offset relative to adjacent electrodes; and(c) a controller configured to selectively energize a subset of the plurality of electrodes.
CROSS-REFERENCES TO RELATED APPLICATIONS

This application is a continuation of U.S. patent application Ser. No. 13/403,920 filed on Feb. 23, 2012, published as U.S. Patent Application Publication No. 2012/0157987, which is a continuation of U.S. patent application Ser. No. 11/864,779 filed on Sep. 28, 2007 (now U.S. Pat. No. 9,125,666), which is a divisional of U.S. patent application Ser. No. 10/938,138, filed on Sep. 10, 2004 (now U.S. Pat. No. 7,291,146), which claims the benefit under 35 USC 119(e) of U.S. Provisional Patent Application No. 60/502,515 filed on Sep. 12, 2003, the full disclosure of each of which is incorporated herein by reference.

US Referenced Citations (1555)
Number Name Date Kind
164184 Kiddee Jun 1875 A
1167014 O'Brien Jan 1916 A
2505358 Gusberg Apr 1950 A
2701559 Cooper Feb 1955 A
3108593 Glassman Oct 1963 A
3108594 Glassman Oct 1963 A
3540431 Mobin Nov 1970 A
3952747 Kimmell Apr 1976 A
3996938 Clark, III Dec 1976 A
4046150 Schwartz et al. Sep 1977 A
4290427 Chin Sep 1981 A
4402686 Medel Sep 1983 A
4483341 Witteles et al. Nov 1984 A
4574804 Kurwa Mar 1986 A
4587975 Salo et al. May 1986 A
4649936 Ungar et al. Mar 1987 A
4682596 Bales et al. Jul 1987 A
4699147 Chilson et al. Oct 1987 A
4709698 Johnston et al. Dec 1987 A
4765331 Petruzzi et al. Aug 1988 A
4770653 Shturman Sep 1988 A
4784162 Ricks et al. Nov 1988 A
4785806 Deckelbaum et al. Nov 1988 A
4790310 Ginsburg et al. Dec 1988 A
4799479 Spears Jan 1989 A
4823791 D'Amelio et al. Apr 1989 A
4830003 Wolff et al. May 1989 A
4849484 Heard Jul 1989 A
4862886 Clarke et al. Sep 1989 A
4887605 Angelsen et al. Dec 1989 A
4784132 Fox et al. Mar 1990 B1
4920979 Bullara May 1990 A
4938766 Jarvik Jul 1990 A
4955377 Lennox et al. Sep 1990 A
4976711 Parins et al. Dec 1990 A
5034010 Kittrell et al. Jul 1991 A
5052402 Bencini et al. Oct 1991 A
5053033 Clarke et al. Oct 1991 A
5071424 Reger et al. Dec 1991 A
5074871 Groshong et al. Dec 1991 A
5098429 Sterzer et al. Mar 1992 A
5098431 Rydell Mar 1992 A
5102402 Dror et al. Apr 1992 A
RE33925 Bales et al. May 1992 E
5109859 Jenkins May 1992 A
5125928 Parins et al. Jun 1992 A
5129396 Rosen et al. Jul 1992 A
5139496 Hed Aug 1992 A
5143836 Hartman et al. Sep 1992 A
5156151 Imran Oct 1992 A
5156610 Reger et al. Oct 1992 A
5158564 Schnepp-Pesch Oct 1992 A
5170802 Mehra Dec 1992 A
5178620 Eggers et al. Jan 1993 A
5178625 Groshong et al. Jan 1993 A
5190540 Lee Mar 1993 A
5191883 Lennox et al. Mar 1993 A
5211651 Reger et al. May 1993 A
5234407 Teirstein et al. Aug 1993 A
5242441 Avitall Sep 1993 A
5251634 Weinberg et al. Oct 1993 A
5254098 Ulrich et al. Oct 1993 A
5255679 Imran Oct 1993 A
5263493 Avitall Nov 1993 A
5267954 Nita et al. Dec 1993 A
5277201 Stern et al. Jan 1994 A
5282484 Reger et al. Feb 1994 A
5286254 Shapland et al. Feb 1994 A
5295484 Marcus Mar 1994 A
5297564 Love et al. Mar 1994 A
5300068 Rosar et al. Apr 1994 A
5301683 Durkan Apr 1994 A
5304115 Pflueger et al. Apr 1994 A
5304121 Sahatjian Apr 1994 A
5304171 Gregory et al. Apr 1994 A
5304173 Kittrell et al. Apr 1994 A
5306250 March et al. Apr 1994 A
5312328 Nita et al. May 1994 A
5314466 Stern et al. May 1994 A
5322064 Lundquist Jun 1994 A
5324255 Passafaro et al. Jun 1994 A
5326341 Lew et al. Jul 1994 A
5326342 Pflueger et al. Jul 1994 A
5330518 Neilson et al. Jul 1994 A
5333614 Feiring Aug 1994 A
5342292 Nita et al. Aug 1994 A
5344395 Whalen et al. Sep 1994 A
5345936 Pomeranz et al. Sep 1994 A
5364392 Warner et al. Nov 1994 A
5365172 Hrovat et al. Nov 1994 A
5368557 Nita et al. Nov 1994 A
5368558 Nita et al. Nov 1994 A
5372138 Crowley et al. Dec 1994 A
5380274 Nita et al. Jan 1995 A
5380319 Saito et al. Jan 1995 A
5382228 Nita et al. Jan 1995 A
5383874 Jackson et al. Jan 1995 A
5383917 Desai et al. Jan 1995 A
5397301 Pflueger et al. Mar 1995 A
5397339 Desai Mar 1995 A
5401272 Perkins et al. Mar 1995 A
5403311 Abele et al. Apr 1995 A
5405318 Nita et al. Apr 1995 A
5405346 Grundy et al. Apr 1995 A
5409000 Imran Apr 1995 A
5417672 Nita et al. May 1995 A
5419767 Eggers et al. May 1995 A
5427118 Nita et al. Jun 1995 A
5432876 Appeldorn et al. Jul 1995 A
5441498 Perkins et al. Aug 1995 A
5447509 Mills et al. Sep 1995 A
5451207 Yock et al. Sep 1995 A
5453091 Taylor et al. Sep 1995 A
5454788 Walker et al. Oct 1995 A
5454809 Janssen Oct 1995 A
5455029 Hartman et al. Oct 1995 A
5456682 Edwards et al. Oct 1995 A
5457042 Hartman et al. Oct 1995 A
5471982 Edwards et al. Dec 1995 A
5474530 Passafaro et al. Dec 1995 A
5478351 Meade et al. Dec 1995 A
5496311 Abele et al. Mar 1996 A
5496312 Klicek et al. Mar 1996 A
5498261 Strul Mar 1996 A
5505201 Grill et al. Apr 1996 A
5505730 Edwards Apr 1996 A
5507744 Tay et al. Apr 1996 A
5522873 Jackman et al. Jun 1996 A
5531520 Grimson et al. Jul 1996 A
5540656 Pflueger et al. Jul 1996 A
5540679 Fram et al. Jul 1996 A
5540681 Strul et al. Jul 1996 A
5542917 Nita et al. Aug 1996 A
5545161 Imran Aug 1996 A
5562100 Kittrell et al. Oct 1996 A
5571122 Kelly et al. Nov 1996 A
5571151 Gregory Nov 1996 A
5573531 Gregory et al. Nov 1996 A
5573533 Strul Nov 1996 A
5584831 McKay Dec 1996 A
5584872 Lafontaine et al. Dec 1996 A
5588962 Nicholas et al. Dec 1996 A
5599346 Edwards et al. Feb 1997 A
5601526 Chapelon et al. Feb 1997 A
5609606 O'Boyle et al. Mar 1997 A
5626576 Janssen May 1997 A
5630837 Crowley May 1997 A
5637090 McGee et al. Jun 1997 A
5643255 Organ Jul 1997 A
5643297 Nordgren et al. Jul 1997 A
5647847 Lafontaine et al. Jul 1997 A
5649923 Gregory et al. Jul 1997 A
5651780 Jackson et al. Jul 1997 A
5653684 Laptewicz et al. Aug 1997 A
5662671 Barbut et al. Sep 1997 A
5665062 Houser Sep 1997 A
5665098 Kelly et al. Sep 1997 A
5666964 Meilus Sep 1997 A
5667490 Keith et al. Sep 1997 A
5672174 Gough et al. Sep 1997 A
5676693 Lafontaine Oct 1997 A
5678296 Fleischhacker et al. Oct 1997 A
5680860 Imran Oct 1997 A
5681282 Eggers et al. Oct 1997 A
RE35656 Feinberg Nov 1997 E
5688266 Edwards et al. Nov 1997 A
5693015 Walker et al. Dec 1997 A
5693029 Leonhardt et al. Dec 1997 A
5693043 Kittrell et al. Dec 1997 A
5693082 Warner et al. Dec 1997 A
5695504 Gifford et al. Dec 1997 A
5697369 Long, Jr. et al. Dec 1997 A
5697909 Eggers et al. Dec 1997 A
5702386 Stern et al. Dec 1997 A
5702433 Taylor et al. Dec 1997 A
5706809 Littmann et al. Jan 1998 A
5713942 Stern et al. Feb 1998 A
5715819 Svenson et al. Feb 1998 A
5722401 Pietroski et al. Mar 1998 A
5735846 Panescu et al. Apr 1998 A
5741214 Ouchi et al. Apr 1998 A
5741248 Stern et al. Apr 1998 A
5741249 Moss et al. Apr 1998 A
5743903 Stern et al. Apr 1998 A
5748347 Erickson May 1998 A
5749914 Janssen May 1998 A
5755682 Knudson et al. May 1998 A
5755715 Stern et al. May 1998 A
5755753 Knowlton et al. May 1998 A
5769847 Panescu et al. Jun 1998 A
5769880 Truckai et al. Jun 1998 A
5775338 Hastings Jul 1998 A
5776174 Van Tassel Jul 1998 A
5779698 Clayman et al. Jul 1998 A
5782760 Schaer Jul 1998 A
5785702 Murphy et al. Jul 1998 A
5792105 Lin et al. Aug 1998 A
5797849 Vesely et al. Aug 1998 A
5797903 Swanson et al. Aug 1998 A
5800484 Gough et al. Sep 1998 A
5800494 Campbell et al. Sep 1998 A
5807306 Shapland et al. Sep 1998 A
5810802 Panescu et al. Sep 1998 A
5810803 Moss et al. Sep 1998 A
5810810 Tay et al. Sep 1998 A
5817092 Behl Oct 1998 A
5817113 Gifford et al. Oct 1998 A
5817144 Gregory et al. Oct 1998 A
5823956 Roth et al. Oct 1998 A
5827203 Nita et al. Oct 1998 A
5827268 Laufer Oct 1998 A
5829447 Stevens et al. Nov 1998 A
5830213 Panescu et al. Nov 1998 A
5830222 Makower Nov 1998 A
5832228 Holden et al. Nov 1998 A
5833593 Liprie Nov 1998 A
5836874 Swanson et al. Nov 1998 A
5840076 Swanson et al. Nov 1998 A
5843016 Lugnani et al. Dec 1998 A
5846238 Jackson et al. Dec 1998 A
5846239 Swanson et al. Dec 1998 A
5846245 McCarthy et al. Dec 1998 A
5848969 Panescu et al. Dec 1998 A
5853411 Whayne et al. Dec 1998 A
5855614 Stevens et al. Jan 1999 A
5860974 Abele Jan 1999 A
5865801 Houser Feb 1999 A
5868735 Lafontaine et al. Feb 1999 A
5868736 Swanson et al. Feb 1999 A
5869127 Zhong Feb 1999 A
5871483 Jackson et al. Feb 1999 A
5871524 Knowlton et al. Feb 1999 A
4788975 Shturman et al. Mar 1999 B1
5875782 Ferrari et al. Mar 1999 A
5876369 Houser Mar 1999 A
5876374 Alba et al. Mar 1999 A
5876397 Edelman et al. Mar 1999 A
5879348 Owens et al. Mar 1999 A
5891114 Chien et al. Apr 1999 A
5891135 Jackson et al. Apr 1999 A
5891136 McGee et al. Apr 1999 A
5891138 Tu et al. Apr 1999 A
5895378 Nita Apr 1999 A
5897552 Edwards et al. Apr 1999 A
5902328 Lafontaine et al. May 1999 A
5904651 Swanson et al. May 1999 A
5904667 Falwell et al. May 1999 A
5904697 Gifford et al. May 1999 A
5904709 Arndt et al. May 1999 A
5906614 Stern et al. May 1999 A
5906623 Peterson May 1999 A
5906636 Casscells et al. May 1999 A
5916192 Nita et al. Jun 1999 A
5916227 Keith et al. Jun 1999 A
5916239 Geddes et al. Jun 1999 A
5919219 Knowlton et al. Jul 1999 A
5924424 Stevens et al. Jul 1999 A
5925038 Panescu et al. Jul 1999 A
5934284 Plaia et al. Aug 1999 A
5935063 Nguyen Aug 1999 A
5938670 Keith et al. Aug 1999 A
5947977 Slepian et al. Sep 1999 A
5948011 Knowlton et al. Sep 1999 A
5951494 Wang et al. Sep 1999 A
5951539 Nita et al. Sep 1999 A
5954717 Behl et al. Sep 1999 A
5957882 Nita et al. Sep 1999 A
5957941 Ream et al. Sep 1999 A
5957969 Warner et al. Sep 1999 A
5961513 Swanson et al. Oct 1999 A
5964757 Ponzi et al. Oct 1999 A
5967976 Larsen et al. Oct 1999 A
5967978 Littmann et al. Oct 1999 A
5967984 Chu et al. Oct 1999 A
5971975 Mills et al. Oct 1999 A
5972026 Laufer et al. Oct 1999 A
5980563 Tu et al. Nov 1999 A
5989208 Nita et al. Nov 1999 A
5989284 Laufer Nov 1999 A
5993462 Pomeranz et al. Nov 1999 A
5997497 Nita et al. Dec 1999 A
5999678 Murphy et al. Dec 1999 A
6004269 Crowley et al. Dec 1999 A
6004316 Laufer et al. Dec 1999 A
6007514 Nita Dec 1999 A
6010522 Barbut et al. Jan 2000 A
6013033 Berger et al. Jan 2000 A
6014590 Whayne et al. Jan 2000 A
6019757 Scheldrup Feb 2000 A
6022309 Celliers et al. Feb 2000 A
6023638 Swanson Feb 2000 A
6024740 Lesh Feb 2000 A
6030611 Gorecki et al. Feb 2000 A
6032675 Rubinsky et al. Mar 2000 A
6033357 Ciezki et al. Mar 2000 A
6033397 Laufer et al. Mar 2000 A
6033398 Farley et al. Mar 2000 A
6036687 Laufer et al. Mar 2000 A
6036689 Tu et al. Mar 2000 A
6041260 Stern et al. Mar 2000 A
6050994 Sherman et al. Apr 2000 A
6053873 Govari et al. Apr 2000 A
6056744 Edwards May 2000 A
6056746 Goble et al. May 2000 A
6063085 Tay et al. May 2000 A
6066096 Smith et al. May 2000 A
6066139 Ryan et al. May 2000 A
6068638 Makower May 2000 A
6068653 Lafontaine May 2000 A
6071277 Farley et al. Jun 2000 A
6071278 Panescu et al. Jun 2000 A
6078839 Carson Jun 2000 A
6079414 Roth Jun 2000 A
6080171 Keith et al. Jun 2000 A
6081749 Ingle et al. Jun 2000 A
6083159 Driscoll, Jr. et al. Jul 2000 A
6086581 Reynolds et al. Jul 2000 A
6091995 Ingle et al. Jul 2000 A
6093166 Knudson et al. Jul 2000 A
6096021 Helm et al. Aug 2000 A
6099526 Whayne et al. Aug 2000 A
6102908 Tu et al. Aug 2000 A
6106477 Miesel et al. Aug 2000 A
6110187 Donlon et al. Aug 2000 A
6114311 Parmacek et al. Sep 2000 A
6117101 Diederich et al. Sep 2000 A
6117128 Gregory Sep 2000 A
6120476 Fung et al. Sep 2000 A
6120516 Selmon et al. Sep 2000 A
6121775 Pearlman Sep 2000 A
6123679 Lafaut et al. Sep 2000 A
6123682 Knudson et al. Sep 2000 A
6123702 Swanson et al. Sep 2000 A
6123703 Tu et al. Sep 2000 A
6123718 Tu et al. Sep 2000 A
6129725 Tu et al. Oct 2000 A
6135997 Laufer et al. Oct 2000 A
6142991 Schatzberger et al. Nov 2000 A
6142993 Whayne et al. Nov 2000 A
6149647 Tu et al. Nov 2000 A
6152899 Farley et al. Nov 2000 A
6152912 Jansen et al. Nov 2000 A
6156046 Passafaro et al. Dec 2000 A
6158250 Tibbals et al. Dec 2000 A
6159187 Park et al. Dec 2000 A
6159225 Makower Dec 2000 A
6161048 Sluijter et al. Dec 2000 A
6162184 Swanson et al. Dec 2000 A
6165163 Chien et al. Dec 2000 A
6165172 Farley et al. Dec 2000 A
6165187 Reger et al. Dec 2000 A
6168594 Lafontaine et al. Jan 2001 B1
6171321 Gifford, III et al. Jan 2001 B1
6179832 Jones et al. Jan 2001 B1
6179835 Panescu et al. Jan 2001 B1
6179859 Bates et al. Jan 2001 B1
6183468 Swanson et al. Feb 2001 B1
6183486 Snow et al. Feb 2001 B1
6190379 Heuser et al. Feb 2001 B1
6191862 Swanson et al. Feb 2001 B1
6197021 Panescu et al. Mar 2001 B1
6200266 Shokrollahi et al. Mar 2001 B1
6203537 Adrian Mar 2001 B1
6203561 Ramee et al. Mar 2001 B1
6210406 Webster Apr 2001 B1
6211247 Goodman Apr 2001 B1
6216044 Kordis Apr 2001 B1
6216704 Ingle et al. Apr 2001 B1
6217576 Tu et al. Apr 2001 B1
6219577 Brown, III et al. Apr 2001 B1
6228076 Winston et al. May 2001 B1
6228109 Tu et al. May 2001 B1
6231516 Keilman et al. May 2001 B1
6231587 Makower May 2001 B1
6235044 Root et al. May 2001 B1
6236883 Ciaccio et al. May 2001 B1
6237605 Vaska et al. May 2001 B1
6238389 Paddock et al. May 2001 B1
6238392 Long May 2001 B1
6241666 Pomeranz et al. Jun 2001 B1
6241753 Knowlton Jun 2001 B1
6245020 Moore et al. Jun 2001 B1
6245045 Stratienko Jun 2001 B1
6248126 Lesser et al. Jun 2001 B1
6251128 Knopp et al. Jun 2001 B1
6258087 Edwards et al. Jul 2001 B1
6273886 Edwards et al. Aug 2001 B1
6280466 Kugler et al. Aug 2001 B1
6283935 Laufer et al. Sep 2001 B1
6283959 Lalonde et al. Sep 2001 B1
6284743 Parmacek et al. Sep 2001 B1
6287323 Hammerslag Sep 2001 B1
6290696 Lafontaine Sep 2001 B1
6292695 Webster, Jr. et al. Sep 2001 B1
6293942 Goble et al. Sep 2001 B1
6293943 Panescu et al. Sep 2001 B1
6296619 Brisken et al. Oct 2001 B1
6298256 Meyer Oct 2001 B1
6299379 Lewis Oct 2001 B1
6299623 Wulfman Oct 2001 B1
6309379 Willard et al. Oct 2001 B1
6309399 Barbut et al. Oct 2001 B1
6311090 Knowlton Oct 2001 B1
6317615 KenKnight et al. Nov 2001 B1
6319242 Patterson et al. Nov 2001 B1
6319251 Tu et al. Nov 2001 B1
6322559 Daulton et al. Nov 2001 B1
6325797 Stewart et al. Dec 2001 B1
6325799 Goble Dec 2001 B1
6328699 Eigler et al. Dec 2001 B1
6346074 Roth Feb 2002 B1
6346104 Daly et al. Feb 2002 B2
6350248 Knudson et al. Feb 2002 B1
6350276 Knowlton Feb 2002 B1
6353751 Swanson et al. Mar 2002 B1
6355029 Joye et al. Mar 2002 B1
6357447 Swanson et al. Mar 2002 B1
6361519 Knudson et al. Mar 2002 B1
6364840 Crowley Apr 2002 B1
6371965 Gifford, III et al. Apr 2002 B2
6375668 Gifford et al. Apr 2002 B1
6377854 Knowlton Apr 2002 B1
6377855 Knowlton Apr 2002 B1
6379352 Reynolds et al. Apr 2002 B1
6379373 Sawhney et al. Apr 2002 B1
6381497 Knowlton Apr 2002 B1
6381498 Knowlton Apr 2002 B1
6383151 Diederich et al. May 2002 B1
6387105 Gifford, III et al. May 2002 B1
6387380 Knowlton May 2002 B1
6389311 Whayne et al. May 2002 B1
6389314 Feiring May 2002 B2
6391024 Sun et al. May 2002 B1
6394096 Constantz May 2002 B1
6394956 Chandrasekaran et al. May 2002 B1
6398780 Farley et al. Jun 2002 B1
6398782 Pecor et al. Jun 2002 B1
6398792 O'Connor Jun 2002 B1
6401720 Stevens et al. Jun 2002 B1
6402719 Ponzi et al. Jun 2002 B1
6405090 Knowlton Jun 2002 B1
6409723 Edwards Jun 2002 B1
6413255 Stern Jul 2002 B1
6421559 Pearlman Jul 2002 B1
6423057 He et al. Jul 2002 B1
6425867 Vaezy et al. Jul 2002 B1
6425912 Knowlton Jul 2002 B1
6427089 Knowlton Jul 2002 B1
6427118 Suzuki Jul 2002 B1
6428534 Joye et al. Aug 2002 B1
6428536 Panescu et al. Aug 2002 B2
6430446 Knowlton Aug 2002 B1
6432102 Joye et al. Aug 2002 B2
6436056 Wang et al. Aug 2002 B1
6438424 Knowlton Aug 2002 B1
6440125 Rentrop Aug 2002 B1
6442413 Silver Aug 2002 B1
6443965 Gifford, III et al. Sep 2002 B1
6445939 Swanson et al. Sep 2002 B1
6447505 McGovern et al. Sep 2002 B2
6447509 Bonnet et al. Sep 2002 B1
6451034 Gifford, III et al. Sep 2002 B1
6451044 Naghavi et al. Sep 2002 B1
6453202 Knowlton Sep 2002 B1
6454737 Nita et al. Sep 2002 B1
6454757 Nita et al. Sep 2002 B1
6454775 Demarais et al. Sep 2002 B1
6458098 Kanesaka Oct 2002 B1
6461378 Knowlton Oct 2002 B1
6468276 McKay Oct 2002 B1
6468297 Williams et al. Oct 2002 B1
6470216 Knowlton Oct 2002 B1
6470219 Edwards et al. Oct 2002 B1
6471696 Berube et al. Oct 2002 B1
6475213 Whayne et al. Nov 2002 B1
6475215 Tanrisever Nov 2002 B1
6475238 Fedida et al. Nov 2002 B1
6477426 Fenn et al. Nov 2002 B1
6480745 Nelson et al. Nov 2002 B2
6481704 Koster et al. Nov 2002 B1
6482202 Goble et al. Nov 2002 B1
6484052 Visuri et al. Nov 2002 B1
6485489 Teirstein et al. Nov 2002 B2
6488679 Swanson et al. Dec 2002 B1
6489307 Phillips et al. Dec 2002 B1
6491705 Gifford, III et al. Dec 2002 B2
6494891 Cornish et al. Dec 2002 B1
6497711 Plaia et al. Dec 2002 B1
6500172 Panescu et al. Dec 2002 B1
6500174 Maguire et al. Dec 2002 B1
6508765 Suorsa et al. Jan 2003 B2
6508804 Sarge et al. Jan 2003 B2
6508815 Strul et al. Jan 2003 B1
6511478 Burnside et al. Jan 2003 B1
6511496 Huter et al. Jan 2003 B1
6511500 Rahme Jan 2003 B1
6514236 Stratienko Feb 2003 B1
6514245 Williams et al. Feb 2003 B1
6514248 Eggers et al. Feb 2003 B1
6517534 McGovern et al. Feb 2003 B1
6517572 Kugler et al. Feb 2003 B2
6522913 Swanson et al. Feb 2003 B2
6522926 Kieval et al. Feb 2003 B1
6524274 Rosenthal et al. Feb 2003 B1
6524299 Tran et al. Feb 2003 B1
6527765 Kelman et al. Mar 2003 B2
6527769 Langberg et al. Mar 2003 B2
6540761 Houser Apr 2003 B2
6542781 Koblish et al. Apr 2003 B1
6544780 Wang Apr 2003 B1
6546272 MacKinnon et al. Apr 2003 B1
6547788 Maguire et al. Apr 2003 B1
6549800 Atalar et al. Apr 2003 B1
6552796 Magnin et al. Apr 2003 B2
6554780 Sampson et al. Apr 2003 B1
6558381 Ingle et al. May 2003 B2
6558382 Jahns et al. May 2003 B2
6564096 Mest May 2003 B2
6565582 Gifford, III et al. May 2003 B2
6569109 Sakurai et al. May 2003 B2
6569177 Dillard et al. May 2003 B1
6570659 Schmitt May 2003 B2
6572551 Smith et al. Jun 2003 B1
6572612 Stewart et al. Jun 2003 B2
6577902 Laufer et al. Jun 2003 B1
6579308 Jansen et al. Jun 2003 B1
6579311 Makower Jun 2003 B1
6582423 Thapliyal et al. Jun 2003 B1
6589238 Edwards et al. Jul 2003 B2
6592526 Lenker Jul 2003 B1
6592567 Levin et al. Jul 2003 B1
6595959 Stratienko Jul 2003 B1
6600956 Maschino et al. Jul 2003 B2
6602242 Fung Aug 2003 B1
6602246 Joye et al. Aug 2003 B1
6605061 Van Tassel et al. Aug 2003 B2
6605084 Acker et al. Aug 2003 B2
6623452 Chien et al. Sep 2003 B2
6623453 Guibert et al. Sep 2003 B1
6632193 Davison et al. Oct 2003 B1
6632196 Houser Oct 2003 B1
6640120 Swanson et al. Oct 2003 B1
6645223 Boyle et al. Nov 2003 B2
6648854 Patterson et al. Nov 2003 B1
6648878 Lafontaine Nov 2003 B2
6648879 Joye et al. Nov 2003 B2
6651672 Roth Nov 2003 B2
6652513 Panescu et al. Nov 2003 B2
6652515 Maguire et al. Nov 2003 B1
6656136 Weng et al. Dec 2003 B1
6658279 Swanson et al. Dec 2003 B2
6659981 Stewart et al. Dec 2003 B2
6666858 Lafontaine Dec 2003 B2
6666863 Wentzel et al. Dec 2003 B2
6669655 Acker et al. Dec 2003 B1
6669692 Nelson et al. Dec 2003 B1
6673040 Samson et al. Jan 2004 B1
6673064 Rentrop Jan 2004 B1
6673066 Werneth Jan 2004 B2
6673090 Root et al. Jan 2004 B2
6673101 Fitzgerald et al. Jan 2004 B1
6673290 Whayne et al. Jan 2004 B1
6676678 Gifford, III et al. Jan 2004 B2
6679268 Stevens et al. Jan 2004 B2
6681773 Murphy et al. Jan 2004 B2
6682541 Gifford, III et al. Jan 2004 B1
6684098 Oshio et al. Jan 2004 B2
6685732 Kramer Feb 2004 B2
6685733 Dae et al. Feb 2004 B1
6689086 Nita et al. Feb 2004 B1
6689148 Sawhney et al. Feb 2004 B2
6690181 Dowdeswell et al. Feb 2004 B1
6692490 Edwards Feb 2004 B1
6695830 Vigil et al. Feb 2004 B2
6695857 Gifford, III et al. Feb 2004 B2
6699241 Rappaport et al. Mar 2004 B2
6699257 Gifford, III et al. Mar 2004 B2
6702748 Nita et al. Mar 2004 B1
6702811 Stewart et al. Mar 2004 B2
6706010 Miki et al. Mar 2004 B1
6706011 Murphy-Chutorian et al. Mar 2004 B1
6706037 Zvuloni et al. Mar 2004 B2
6709431 Lafontaine Mar 2004 B2
6711429 Gilboa et al. Mar 2004 B1
6712815 Sampson et al. Mar 2004 B2
6714822 King et al. Mar 2004 B2
6716184 Vaezy et al. Apr 2004 B2
6720350 Kunz et al. Apr 2004 B2
6723043 Kleeman et al. Apr 2004 B2
6723064 Babaev Apr 2004 B2
6736811 Panescu et al. May 2004 B2
6743184 Sampson et al. Jun 2004 B2
6746401 Panescu Jun 2004 B2
6746464 Makower Jun 2004 B1
6746474 Saadat Jun 2004 B2
6748953 Sherry et al. Jun 2004 B2
6749607 Edwards et al. Jun 2004 B2
6752805 Maguire et al. Jun 2004 B2
6760616 Hoey et al. Jul 2004 B2
6763261 Casscells, III et al. Jul 2004 B2
6764501 Ganz Jul 2004 B2
6769433 Zikorus et al. Aug 2004 B2
6770070 Balbierz Aug 2004 B1
6771996 Bowe et al. Aug 2004 B2
6773433 Stewart et al. Aug 2004 B2
6786900 Joye et al. Sep 2004 B2
6786901 Joye et al. Sep 2004 B2
6786904 Döscher et al. Sep 2004 B2
6788977 Fenn et al. Sep 2004 B2
6790206 Panescu Sep 2004 B2
6790222 Kugler et al. Sep 2004 B2
6796981 Wham et al. Sep 2004 B2
6797933 Mendis et al. Sep 2004 B1
6797960 Spartiotis et al. Sep 2004 B1
6800075 Mische et al. Oct 2004 B2
6802857 Walsh et al. Oct 2004 B1
6807444 Tu et al. Oct 2004 B2
6811550 Holland et al. Nov 2004 B2
6813520 Truckai et al. Nov 2004 B2
6814730 Li Nov 2004 B2
6814733 Schwartz et al. Nov 2004 B2
6823205 Jara Nov 2004 B1
6824516 Batten et al. Nov 2004 B2
6827726 Parodi Dec 2004 B2
6827926 Robinson et al. Dec 2004 B2
6829497 Mogul Dec 2004 B2
6830568 Kesten et al. Dec 2004 B1
6837886 Collins et al. Jan 2005 B2
6837888 Ciarrocca et al. Jan 2005 B2
6845267 Harrison Jan 2005 B2
6847848 Sterzer Jan 2005 B2
6849073 Hoey et al. Feb 2005 B2
6849075 Bertolero et al. Feb 2005 B2
6853425 Kim et al. Feb 2005 B2
6855123 Nita Feb 2005 B2
6855143 Davison Feb 2005 B2
6869431 Maguire et al. Mar 2005 B2
6872183 Sampson et al. Mar 2005 B2
6884260 Kugler et al. Apr 2005 B2
6889694 Hooven May 2005 B2
6893436 Woodard et al. May 2005 B2
6895077 Karellas et al. May 2005 B2
6895265 Silver May 2005 B2
6898454 Atalar et al. May 2005 B2
6899711 Stewart et al. May 2005 B2
6899718 Gifford, III et al. May 2005 B2
6905494 Yon et al. Jun 2005 B2
6908462 Joye et al. Jun 2005 B2
6909009 Koridze Jun 2005 B2
6911026 Hall et al. Jun 2005 B1
6915806 Pacek et al. Jul 2005 B2
6923805 LaFontaine et al. Aug 2005 B1
6926246 Ginggen Aug 2005 B2
6926713 Rioux et al. Aug 2005 B2
6926716 Baker et al. Aug 2005 B2
6929009 Makower et al. Aug 2005 B2
6929632 Nita et al. Aug 2005 B2
6929639 Lafontaine Aug 2005 B2
6932776 Carr Aug 2005 B2
6936047 Nasab et al. Aug 2005 B2
6942620 Nita et al. Sep 2005 B2
6942657 Sinofsky et al. Sep 2005 B2
6942677 Nita et al. Sep 2005 B2
6942692 Landau et al. Sep 2005 B2
6949097 Stewart et al. Sep 2005 B2
6949121 Laguna Sep 2005 B1
6952615 Satake Oct 2005 B2
6953425 Brister Oct 2005 B2
6955174 Joye et al. Oct 2005 B2
6955175 Stevens et al. Oct 2005 B2
6958075 Mon et al. Oct 2005 B2
6959711 Murphy et al. Nov 2005 B2
6960207 Vanney et al. Nov 2005 B2
6962584 Stone et al. Nov 2005 B1
6964660 Maguire et al. Nov 2005 B2
6966908 Maguire et al. Nov 2005 B2
6972015 Joye et al. Dec 2005 B2
6972024 Kilpatrick et al. Dec 2005 B1
6974456 Edwards et al. Dec 2005 B2
6978174 Gelfand et al. Dec 2005 B2
6979329 Burnside et al. Dec 2005 B2
6979420 Weber Dec 2005 B2
6984238 Gifford, III et al. Jan 2006 B2
6985774 Kieval et al. Jan 2006 B2
6986739 Warren et al. Jan 2006 B2
6989009 Lafontaine Jan 2006 B2
6989010 Francischelli et al. Jan 2006 B2
6991617 Hektner et al. Jan 2006 B2
7001378 Yon et al. Feb 2006 B2
7006858 Silver et al. Feb 2006 B2
7008667 Chudzik et al. Mar 2006 B2
7011508 Lum Mar 2006 B2
7022105 Edwards Apr 2006 B1
7022120 Lafontaine Apr 2006 B2
7025767 Schaefer et al. Apr 2006 B2
7033322 Silver Apr 2006 B2
7033372 Cahalan Apr 2006 B1
7041098 Farley et al. May 2006 B2
7050848 Hoey et al. May 2006 B2
7063670 Sampson et al. Jun 2006 B2
7063679 Maguire et al. Jun 2006 B2
7063719 Jansen et al. Jun 2006 B2
7066895 Podany Jun 2006 B2
7066900 Botto et al. Jun 2006 B2
7066904 Rosenthal et al. Jun 2006 B2
7072720 Puskas Jul 2006 B2
7074217 Strul et al. Jul 2006 B2
7081112 Joye et al. Jul 2006 B2
7081114 Rashidi Jul 2006 B2
7083614 Fjield et al. Aug 2006 B2
7084276 Vu et al. Aug 2006 B2
7087026 Callister et al. Aug 2006 B2
7087051 Bourne et al. Aug 2006 B2
7087052 Sampson et al. Aug 2006 B2
7087053 Vanney Aug 2006 B2
7089065 Westlund et al. Aug 2006 B2
7097641 Arless et al. Aug 2006 B1
7100614 Stevens et al. Sep 2006 B2
7101368 Lafontaine Sep 2006 B2
7104983 Grasso, III et al. Sep 2006 B2
7104987 Biggs et al. Sep 2006 B2
7108715 Lawrence-Brown et al. Sep 2006 B2
7112196 Brosch et al. Sep 2006 B2
7112198 Satake Sep 2006 B2
7112211 Gifford, III et al. Sep 2006 B2
7122019 Kesten et al. Oct 2006 B1
7122033 Wood Oct 2006 B2
7134438 Makower et al. Nov 2006 B2
7137963 Nita et al. Nov 2006 B2
7137980 Buysse et al. Nov 2006 B2
7153315 Miller Dec 2006 B2
7155271 Halperin et al. Dec 2006 B2
7157491 Mewshaw et al. Jan 2007 B2
7157492 Mewshaw et al. Jan 2007 B2
7158832 Kieval et al. Jan 2007 B2
7160296 Pearson et al. Jan 2007 B2
7162303 Levin et al. Jan 2007 B2
7165551 Edwards et al. Jan 2007 B2
7169144 Hoey et al. Jan 2007 B2
7172589 Lafontaine Feb 2007 B2
7172610 Heitzmann et al. Feb 2007 B2
7181261 Silver et al. Feb 2007 B2
7184811 Phan et al. Feb 2007 B2
7184827 Edwards Feb 2007 B1
7189227 Lafontaine Mar 2007 B2
7192427 Chapelon et al. Mar 2007 B2
7192586 Bander Mar 2007 B2
7197354 Sobe Mar 2007 B2
7198632 Lim et al. Apr 2007 B2
7200445 Dalbec et al. Apr 2007 B1
7201749 Govari et al. Apr 2007 B2
7203537 Mower Apr 2007 B2
7214234 Rapacki et al. May 2007 B2
7220233 Nita et al. May 2007 B2
7220239 Wilson et al. May 2007 B2
7220257 Lafontaine May 2007 B1
7220270 Sawhney et al. May 2007 B2
7232458 Saadat Jun 2007 B2
7232459 Greenberg et al. Jun 2007 B2
7238184 Megerman et al. Jul 2007 B2
7241273 Maguire et al. Jul 2007 B2
7241736 Hunter et al. Jul 2007 B2
7247141 Makin et al. Jul 2007 B2
7250041 Chiu et al. Jul 2007 B2
7250440 Mewshaw et al. Jul 2007 B2
7252664 Nasab et al. Aug 2007 B2
7252679 Fischell et al. Aug 2007 B2
7264619 Venturelli Sep 2007 B2
7279600 Mewshaw et al. Oct 2007 B2
7280863 Shachar Oct 2007 B2
7282213 Schroeder et al. Oct 2007 B2
7285119 Stewart et al. Oct 2007 B2
7285120 Im et al. Oct 2007 B2
7288089 Yon et al. Oct 2007 B2
7288096 Chin Oct 2007 B2
7291146 Steinke et al. Nov 2007 B2
7293562 Malecki et al. Nov 2007 B2
7294125 Phalen et al. Nov 2007 B2
7294126 Sampson et al. Nov 2007 B2
7294127 Leung et al. Nov 2007 B2
7297131 Nita Nov 2007 B2
7297475 Koiwai et al. Nov 2007 B2
7300433 Lane et al. Nov 2007 B2
7301108 Egitto et al. Nov 2007 B2
7310150 Guillermo et al. Dec 2007 B2
7313430 Urquhart et al. Dec 2007 B2
7314483 Landau et al. Jan 2008 B2
7317077 Averback et al. Jan 2008 B2
7323006 Andreas et al. Jan 2008 B2
7326206 Paul et al. Feb 2008 B2
7326226 Root et al. Feb 2008 B2
7326235 Edwards Feb 2008 B2
7326237 DePalma et al. Feb 2008 B2
7329236 Kesten et al. Feb 2008 B2
7335180 Nita et al. Feb 2008 B2
7335192 Keren et al. Feb 2008 B2
7338467 Lutter Mar 2008 B2
7341570 Keren et al. Mar 2008 B2
7343195 Strommer et al. Mar 2008 B2
7347857 Anderson et al. Mar 2008 B2
7348003 Salcedo et al. Mar 2008 B2
7352593 Zeng et al. Apr 2008 B2
7354927 Vu Apr 2008 B2
7359732 Kim et al. Apr 2008 B2
7361341 Salcedo et al. Apr 2008 B2
7364566 Elkins et al. Apr 2008 B2
7367970 Govari et al. May 2008 B2
7367975 Malecki et al. May 2008 B2
7371231 Rioux et al. May 2008 B2
7387126 Cox et al. Jun 2008 B2
7393338 Nita Jul 2008 B2
7396355 Goldman et al. Jul 2008 B2
7402151 Rosenman et al. Jul 2008 B2
7402312 Rosen et al. Jul 2008 B2
7404824 Webler et al. Jul 2008 B1
7406970 Zikorus et al. Aug 2008 B2
7407502 Strul et al. Aug 2008 B2
7407506 Makower Aug 2008 B2
7407671 McBride et al. Aug 2008 B2
7408021 Averback et al. Aug 2008 B2
7410486 Fuimaono et al. Aug 2008 B2
7413556 Zhang et al. Aug 2008 B2
7425212 Danek et al. Sep 2008 B1
7426409 Casscells, III et al. Sep 2008 B2
7435248 Taimisto et al. Oct 2008 B2
7447453 Kim et al. Nov 2008 B2
7449018 Kramer Nov 2008 B2
7452538 Ni et al. Nov 2008 B2
7473890 Grier et al. Jan 2009 B2
7476384 Ni et al. Jan 2009 B2
7479157 Weber et al. Jan 2009 B2
7481803 Kesten et al. Jan 2009 B2
7485104 Kieval Feb 2009 B2
7486805 Krattiger Feb 2009 B2
7487780 Hooven Feb 2009 B2
7493154 Bonner et al. Feb 2009 B2
7494485 Beck et al. Feb 2009 B2
7494486 Mische et al. Feb 2009 B2
7494488 Weber Feb 2009 B2
7494661 Sanders Feb 2009 B2
7495439 Wiggins Feb 2009 B2
7497858 Chapelon et al. Mar 2009 B2
7499745 Littrup et al. Mar 2009 B2
7500985 Saadat Mar 2009 B2
7505812 Eggers et al. Mar 2009 B1
7505816 Schmeling et al. Mar 2009 B2
7507233 Littrup et al. Mar 2009 B2
7507235 Keogh et al. Mar 2009 B2
7511494 Wedeen Mar 2009 B2
7512445 Truckai et al. Mar 2009 B2
7527643 Case et al. May 2009 B2
7529589 Williams et al. May 2009 B2
7540852 Nita et al. Jun 2009 B2
7540870 Babaev Jun 2009 B2
RE40863 Tay et al. Jul 2009 E
7556624 Laufer et al. Jul 2009 B2
7558625 Levin et al. Jul 2009 B2
7563247 Maguire et al. Jul 2009 B2
7566319 McAuley et al. Jul 2009 B2
7569052 Phan et al. Aug 2009 B2
7582111 Krolik et al. Sep 2009 B2
7584004 Caparso et al. Sep 2009 B2
7585835 Hill et al. Sep 2009 B2
7591996 Hwang et al. Sep 2009 B2
7597704 Frazier et al. Oct 2009 B2
7598228 Hattori et al. Oct 2009 B2
7599730 Hunter et al. Oct 2009 B2
7603166 Casscells, III et al. Oct 2009 B2
7604608 Nita et al. Oct 2009 B2
7604633 Truckai et al. Oct 2009 B2
7615015 Coleman Nov 2009 B2
7615072 Rust et al. Nov 2009 B2
7617005 Demarais et al. Nov 2009 B2
7620451 Demarais et al. Nov 2009 B2
7621902 Nita et al. Nov 2009 B2
7621929 Nita et al. Nov 2009 B2
7626015 Feinstein et al. Dec 2009 B2
7626235 Kinoshita Dec 2009 B2
7632268 Edwards et al. Dec 2009 B2
7632845 Vu et al. Dec 2009 B2
7635383 Gumm Dec 2009 B2
7640046 Pastore et al. Dec 2009 B2
7641633 Laufer et al. Jan 2010 B2
7641679 Joye et al. Jan 2010 B2
7646544 Batchko et al. Jan 2010 B2
7647115 Levin et al. Jan 2010 B2
7653438 Deem et al. Jan 2010 B2
7655006 Sauvageau et al. Feb 2010 B2
7662114 Seip et al. Feb 2010 B2
7664548 Amurthur et al. Feb 2010 B2
7670279 Gertner Mar 2010 B2
7670335 Keidar Mar 2010 B2
7671084 Mewshaw et al. Mar 2010 B2
7678104 Keidar Mar 2010 B2
7678106 Lee Mar 2010 B2
7678108 Chrisitian et al. Mar 2010 B2
7691080 Seward et al. Apr 2010 B2
7699809 Urmey Apr 2010 B2
7706882 Francischelli et al. Apr 2010 B2
7715912 Rezai et al. May 2010 B2
7717853 Nita May 2010 B2
7717909 Strul et al. May 2010 B2
7717948 Demarais et al. May 2010 B2
7722539 Carter et al. May 2010 B2
7725157 Dumoulin et al. May 2010 B2
7727178 Wilson et al. Jun 2010 B2
7736317 Stephens et al. Jun 2010 B2
7736360 Mody et al. Jun 2010 B2
7736362 Eberl et al. Jun 2010 B2
7738952 Yun et al. Jun 2010 B2
7740629 Anderson et al. Jun 2010 B2
7741299 Feinstein et al. Jun 2010 B2
7742795 Stone et al. Jun 2010 B2
7744594 Yamazaki et al. Jun 2010 B2
7753907 DiMatteo et al. Jul 2010 B2
7756583 Demarais et al. Jul 2010 B2
7758510 Nita et al. Jul 2010 B2
7758520 Griffin et al. Jul 2010 B2
7759315 Cuzzocrea et al. Jul 2010 B2
7766833 Lee et al. Aug 2010 B2
7766878 Tremaglio, Jr. et al. Aug 2010 B2
7766892 Keren et al. Aug 2010 B2
7767844 Lee et al. Aug 2010 B2
7769427 Shachar Aug 2010 B2
7771372 Wilson Aug 2010 B2
7771421 Stewart et al. Aug 2010 B2
7776967 Perry et al. Aug 2010 B2
7777486 Hargreaves et al. Aug 2010 B2
7780660 Bourne et al. Aug 2010 B2
7789876 Zikorus et al. Sep 2010 B2
7792568 Zhong et al. Sep 2010 B2
7799021 Leung et al. Sep 2010 B2
7803168 Gifford et al. Sep 2010 B2
7806871 Li et al. Oct 2010 B2
7811265 Hering et al. Oct 2010 B2
7811281 Rentrop Oct 2010 B1
7811313 Mon et al. Oct 2010 B2
7816511 Kawashima et al. Oct 2010 B2
7818053 Kassab Oct 2010 B2
7819866 Bednarek Oct 2010 B2
7822460 Halperin et al. Oct 2010 B2
7828837 Khoury Nov 2010 B2
7832407 Gertner Nov 2010 B2
7833220 Mon et al. Nov 2010 B2
7837676 Sinelnikov et al. Nov 2010 B2
7837720 Mon Nov 2010 B2
7841978 Gertner Nov 2010 B2
7846157 Kozel Dec 2010 B2
7846160 Payne et al. Dec 2010 B2
7846172 Makower Dec 2010 B2
7849860 Makower et al. Dec 2010 B2
7850685 Kunis et al. Dec 2010 B2
7853333 Demarais Dec 2010 B2
7854734 Biggs et al. Dec 2010 B2
7857756 Warren et al. Dec 2010 B2
7862565 Eder et al. Jan 2011 B2
7863897 Slocum, Jr. et al. Jan 2011 B2
7869854 Shachar et al. Jan 2011 B2
7873417 Demarais et al. Jan 2011 B2
7887538 Bleich et al. Feb 2011 B2
7894905 Pless et al. Feb 2011 B2
7896873 Hiller et al. Mar 2011 B2
7901400 Wham et al. Mar 2011 B2
7901402 Jones et al. Mar 2011 B2
7901420 Dunn Mar 2011 B2
7905862 Sampson Mar 2011 B2
7918850 Govari et al. Apr 2011 B2
7927370 Webler et al. Apr 2011 B2
7937143 Demarais et al. May 2011 B2
7938830 Saadat et al. May 2011 B2
7942874 Eder et al. May 2011 B2
7942928 Webler et al. May 2011 B2
7946976 Gertner May 2011 B2
7950397 Thapliyal et al. May 2011 B2
7955293 Nita et al. Jun 2011 B2
7956613 Wald Jun 2011 B2
7959627 Utley et al. Jun 2011 B2
7962854 Vance et al. Jun 2011 B2
7967782 Laufer et al. Jun 2011 B2
7967808 Fitzgerald et al. Jun 2011 B2
7972327 Eberl et al. Jul 2011 B2
7972330 Alejandro et al. Jul 2011 B2
7983751 Zdeblick et al. Jul 2011 B2
8001976 Gertner Aug 2011 B2
8007440 Magnin et al. Aug 2011 B2
8012147 Lafontaine Sep 2011 B2
8019435 Hastings et al. Sep 2011 B2
8021362 Deem et al. Sep 2011 B2
8021413 Dierking et al. Sep 2011 B2
8025661 Arnold et al. Sep 2011 B2
8027718 Spinner et al. Sep 2011 B2
8031927 Karl et al. Oct 2011 B2
8033284 Porter et al. Oct 2011 B2
8048144 Thistle et al. Nov 2011 B2
8052636 Moll et al. Nov 2011 B2
8052700 Dunn Nov 2011 B2
8062289 Babaev Nov 2011 B2
8075580 Makower Dec 2011 B2
8080006 Lafontaine et al. Dec 2011 B2
8088127 Mayse et al. Jan 2012 B2
8116883 Williams et al. Feb 2012 B2
8119183 O'Donoghue et al. Feb 2012 B2
8120518 Jang et al. Feb 2012 B2
8123741 Marrouche et al. Feb 2012 B2
8128617 Bencini et al. Mar 2012 B2
8131371 Demarals et al. Mar 2012 B2
8131372 Levin et al. Mar 2012 B2
8131382 Asada Mar 2012 B2
8137274 Weng et al. Mar 2012 B2
8140170 Rezai et al. Mar 2012 B2
8143316 Ueno Mar 2012 B2
8145316 Deem et al. Mar 2012 B2
8145317 Demarais et al. Mar 2012 B2
8150518 Levin et al. Apr 2012 B2
8150519 Demarais et al. Apr 2012 B2
8150520 Demarais et al. Apr 2012 B2
8152830 Gumm Apr 2012 B2
8162933 Francischelli et al. Apr 2012 B2
8175711 Demarais et al. May 2012 B2
8187261 Watson May 2012 B2
8190238 Moll et al. May 2012 B2
8192053 Owen et al. Jun 2012 B2
8198611 LaFontaine et al. Jun 2012 B2
8214056 Hoffer et al. Jul 2012 B2
8221407 Phan et al. Jul 2012 B2
8226637 Satake Jul 2012 B2
8231617 Satake Jul 2012 B2
8241217 Chiang et al. Aug 2012 B2
8257724 Cromack et al. Sep 2012 B2
8257725 Cromack et al. Sep 2012 B2
8260397 Ruff et al. Sep 2012 B2
8263104 Ho et al. Sep 2012 B2
8273023 Razavi Sep 2012 B2
8277379 Lau et al. Oct 2012 B2
8287524 Siegel Oct 2012 B2
8287532 Carroll et al. Oct 2012 B2
8292881 Brannan et al. Oct 2012 B2
8293703 Averback et al. Oct 2012 B2
8295902 Salahieh et al. Oct 2012 B2
8295912 Gertner Oct 2012 B2
8308722 Ormsby et al. Nov 2012 B2
8317776 Ferren et al. Nov 2012 B2
8317810 Stangenes et al. Nov 2012 B2
8329179 Ni et al. Dec 2012 B2
8336705 Okahisa Dec 2012 B2
8343031 Gertner Jan 2013 B2
8343145 Brannan Jan 2013 B2
8347891 Demarais et al. Jan 2013 B2
8353945 Andreas et al. Jan 2013 B2
8364237 Stone et al. Jan 2013 B2
8366615 Razavi Feb 2013 B2
8382697 Brenneman et al. Feb 2013 B2
8388680 Starksen et al. Mar 2013 B2
8396548 Perry et al. Mar 2013 B2
8398629 Thistle Mar 2013 B2
8401667 Gustus et al. Mar 2013 B2
8403881 Ferren et al. Mar 2013 B2
8406877 Smith et al. Mar 2013 B2
8409172 Moll et al. Apr 2013 B2
8409193 Young et al. Apr 2013 B2
8409195 Young Apr 2013 B2
8418362 Zerfas et al. Apr 2013 B2
8452988 Wang May 2013 B2
8454594 Demarais et al. Jun 2013 B2
8460358 Andreas et al. Jun 2013 B2
8465452 Kassab Jun 2013 B2
8469919 Ingle et al. Jun 2013 B2
8473067 Hastings et al. Jun 2013 B2
8480663 Ingle et al. Jul 2013 B2
8485992 Griffin et al. Jul 2013 B2
8486060 Kotmel et al. Jul 2013 B2
8486063 Werneth et al. Jul 2013 B2
8488591 Miali et al. Jul 2013 B2
20010007070 Stewart et al. Jul 2001 A1
20010039419 Francischelli et al. Nov 2001 A1
20010051774 Littrup et al. Dec 2001 A1
20020004631 Jenkins et al. Jan 2002 A1
20020022864 Mahvi et al. Feb 2002 A1
20020042639 Murphy-Chutorian et al. Apr 2002 A1
20020045811 Kittrell et al. Apr 2002 A1
20020045890 Celliers et al. Apr 2002 A1
20020062123 McClurken et al. May 2002 A1
20020062146 Makower et al. May 2002 A1
20020065542 Lax et al. May 2002 A1
20020072686 Hoey et al. Jun 2002 A1
20020077592 Barry Jun 2002 A1
20020082552 Ding et al. Jun 2002 A1
20020087151 Mody et al. Jul 2002 A1
20020087156 Maguire et al. Jul 2002 A1
20020091381 Edwards Jul 2002 A1
20020095197 Lardo et al. Jul 2002 A1
20020107511 Collins et al. Aug 2002 A1
20020107536 Hussein Aug 2002 A1
20020111618 Stewart et al. Aug 2002 A1
20020143324 Edwards Oct 2002 A1
20020147480 Mamayek Oct 2002 A1
20020169444 Mest et al. Nov 2002 A1
20020198520 Coen et al. Dec 2002 A1
20030004510 Wham et al. Jan 2003 A1
20030028114 Casscells, III et al. Feb 2003 A1
20030050635 Truckai et al. Mar 2003 A1
20030060857 Perrson et al. Mar 2003 A1
20030060858 Kieval et al. Mar 2003 A1
20030065317 Rudie et al. Apr 2003 A1
20030069619 Fenn et al. Apr 2003 A1
20030088189 Tu et al. May 2003 A1
20030092995 Thompson May 2003 A1
20030114791 Rosenthal et al. Jun 2003 A1
20030139689 Shturman et al. Jul 2003 A1
20030195501 Sherman et al. Oct 2003 A1
20030199747 Michlitsch et al. Oct 2003 A1
20030212394 Pearson et al. Nov 2003 A1
20030220639 Chapelon et al. Nov 2003 A1
20030229340 Sherry et al. Dec 2003 A1
20030229384 Mon Dec 2003 A1
20040000633 Casper et al. Jan 2004 A1
20040006359 Laguna Jan 2004 A1
20040010118 Zerhusen et al. Jan 2004 A1
20040019348 Stevens et al. Jan 2004 A1
20040024371 Plicchi et al. Feb 2004 A1
20040043030 Griffiths et al. Mar 2004 A1
20040062852 Schroeder et al. Apr 2004 A1
20040064090 Keren et al. Apr 2004 A1
20040064093 Hektner et al. Apr 2004 A1
20040073206 Foley et al. Apr 2004 A1
20040088002 Boyle et al. May 2004 A1
20040093055 Bartorelli et al. May 2004 A1
20040106871 Hunyor et al. Jun 2004 A1
20040111016 Casscells, III et al. Jun 2004 A1
20040117032 Roth Jun 2004 A1
20040122421 Wood Jun 2004 A1
20040147915 Hasebe Jul 2004 A1
20040162555 Farley et al. Aug 2004 A1
20040167506 Chen Aug 2004 A1
20040181165 Hoey et al. Sep 2004 A1
20040186356 O'Malley et al. Sep 2004 A1
20040186468 Edwards Sep 2004 A1
20040187875 He et al. Sep 2004 A1
20040193211 Voegele et al. Sep 2004 A1
20040220556 Cooper et al. Nov 2004 A1
20040243022 Carney et al. Dec 2004 A1
20040243199 Mon et al. Dec 2004 A1
20040253304 Gross et al. Dec 2004 A1
20040267250 Yon et al. Dec 2004 A1
20050010095 Stewart et al. Jan 2005 A1
20050010208 Winston et al. Jan 2005 A1
20050015125 Mioduski et al. Jan 2005 A1
20050033136 Govari et al. Feb 2005 A1
20050080374 Esch et al. Apr 2005 A1
20050090820 Cornelius et al. Apr 2005 A1
20050096647 Steinke et al. May 2005 A1
20050129616 Salcedo et al. Jun 2005 A1
20050137180 Robinson et al. Jun 2005 A1
20050143817 Hunter et al. Jun 2005 A1
20050148842 Wang et al. Jul 2005 A1
20050149069 Bertolero et al. Jul 2005 A1
20050149080 Hunter et al. Jul 2005 A1
20050149158 Hunter et al. Jul 2005 A1
20050149173 Hunter et al. Jul 2005 A1
20050149175 Hunter et al. Jul 2005 A1
20050154277 Tang et al. Jul 2005 A1
20050154445 Hunter et al. Jul 2005 A1
20050154453 Hunter et al. Jul 2005 A1
20050154454 Hunter et al. Jul 2005 A1
20050165389 Swain et al. Jul 2005 A1
20050165391 Maguire et al. Jul 2005 A1
20050165467 Hunter et al. Jul 2005 A1
20050165488 Hunter et al. Jul 2005 A1
20050175661 Hunter et al. Aug 2005 A1
20050175662 Hunter et al. Aug 2005 A1
20050175663 Hunter et al. Aug 2005 A1
20050177103 Hunter et al. Aug 2005 A1
20050177225 Hunter et al. Aug 2005 A1
20050181004 Hunter et al. Aug 2005 A1
20050181008 Hunter et al. Aug 2005 A1
20050181011 Hunter et al. Aug 2005 A1
20050181977 Hunter et al. Aug 2005 A1
20050182479 Bonsignore et al. Aug 2005 A1
20050183728 Hunter et al. Aug 2005 A1
20050186242 Hunter et al. Aug 2005 A1
20050186243 Hunter et al. Aug 2005 A1
20050191331 Hunter et al. Sep 2005 A1
20050203410 Jenkins Sep 2005 A1
20050203434 Kassab Sep 2005 A1
20050203498 Mon et al. Sep 2005 A1
20050209587 Joye et al. Sep 2005 A1
20050214205 Salcedo et al. Sep 2005 A1
20050214207 Salcedo et al. Sep 2005 A1
20050214208 Salcedo et al. Sep 2005 A1
20050214209 Salcedo et al. Sep 2005 A1
20050214210 Salcedo et al. Sep 2005 A1
20050214268 Cavanagh et al. Sep 2005 A1
20050228286 Messerly et al. Oct 2005 A1
20050228415 Gertner Oct 2005 A1
20050228460 Levin et al. Oct 2005 A1
20050232921 Rosen et al. Oct 2005 A1
20050234312 Suzuki et al. Oct 2005 A1
20050245862 Seward Nov 2005 A1
20050251116 Steinke et al. Nov 2005 A1
20050252553 Ginggen Nov 2005 A1
20050256398 Hastings et al. Nov 2005 A1
20050267556 Shuros et al. Dec 2005 A1
20050283195 Pastore et al. Dec 2005 A1
20060004323 Chang et al. Jan 2006 A1
20060018949 Ammon et al. Jan 2006 A1
20060024564 Manclaw Feb 2006 A1
20060025765 Landman et al. Feb 2006 A1
20060062786 Salcedo et al. Mar 2006 A1
20060083194 Dhrimaj et al. Apr 2006 A1
20060085054 Zikorus et al. Apr 2006 A1
20060089637 Werneth et al. Apr 2006 A1
20060089638 Carmel et al. Apr 2006 A1
20060095096 DeBenedictis et al. May 2006 A1
20060106375 Werneth et al. May 2006 A1
20060142790 Gertner Jun 2006 A1
20060147492 Hunter et al. Jul 2006 A1
20060149166 Zvuloni Jul 2006 A1
20060167106 Zhang et al. Jul 2006 A1
20060167498 DiLorenzo Jul 2006 A1
20060171895 Bucay-Couto Aug 2006 A1
20060184060 Belalcazar et al. Aug 2006 A1
20060184221 Stewart et al. Aug 2006 A1
20060195139 Gertner Aug 2006 A1
20060206150 Demarais et al. Sep 2006 A1
20060224153 Fischell et al. Oct 2006 A1
20060235286 Stone et al. Oct 2006 A1
20060239921 Mangat et al. Oct 2006 A1
20060240070 Cromack et al. Oct 2006 A1
20060246143 Ege Nov 2006 A1
20060247266 Yamada et al. Nov 2006 A1
20060247760 Ganesan et al. Nov 2006 A1
20060263393 Demopulos et al. Nov 2006 A1
20060269555 Salcedo et al. Nov 2006 A1
20060271111 Demarais et al. Nov 2006 A1
20060280858 Kokish Dec 2006 A1
20060287644 Inganas et al. Dec 2006 A1
20070016184 Cropper et al. Jan 2007 A1
20070016274 Boveja et al. Jan 2007 A1
20070027390 Maschke et al. Feb 2007 A1
20070043077 Mewshaw et al. Feb 2007 A1
20070043409 Brian et al. Feb 2007 A1
20070049924 Rahn Mar 2007 A1
20070066972 Ormsby et al. Mar 2007 A1
20070073151 Lee Mar 2007 A1
20070078498 Rezai et al. Apr 2007 A1
20070093710 Maschke Apr 2007 A1
20070100405 Thompson et al. May 2007 A1
20070106247 Burnett et al. May 2007 A1
20070112327 Yun et al. May 2007 A1
20070118107 Francischelli et al. May 2007 A1
20070129760 Demarais et al. Jun 2007 A1
20070129761 Demarais et al. Jun 2007 A1
20070135875 Demarais et al. Jun 2007 A1
20070149963 Matsukuma et al. Jun 2007 A1
20070162109 Davila et al. Jul 2007 A1
20070173805 Weinberg et al. Jul 2007 A1
20070173899 Levin et al. Jul 2007 A1
20070179496 Swoyer et al. Aug 2007 A1
20070197891 Shachar et al. Aug 2007 A1
20070203480 Mody et al. Aug 2007 A1
20070207186 Scanlon et al. Sep 2007 A1
20070208134 Hunter et al. Sep 2007 A1
20070208210 Gelfand et al. Sep 2007 A1
20070208256 Marilla Sep 2007 A1
20070208301 Evard et al. Sep 2007 A1
20070219576 Cangialosi Sep 2007 A1
20070225781 Saadat et al. Sep 2007 A1
20070233170 Gertner Oct 2007 A1
20070239062 Chopra et al. Oct 2007 A1
20070248639 Demopulos et al. Oct 2007 A1
20070249703 Mewshaw et al. Oct 2007 A1
20070254833 Hunter et al. Nov 2007 A1
20070265687 Deem et al. Nov 2007 A1
20070278103 Hoerr et al. Dec 2007 A1
20070282302 Wachsman et al. Dec 2007 A1
20070292411 Salcedo et al. Dec 2007 A1
20070293782 Marino Dec 2007 A1
20070299043 Hunter et al. Dec 2007 A1
20080004673 Rossing et al. Jan 2008 A1
20080009927 Vilims Jan 2008 A1
20080015501 Gertner Jan 2008 A1
20080021408 Jacobsen et al. Jan 2008 A1
20080033049 Mewshaw Feb 2008 A1
20080039746 Hissong et al. Feb 2008 A1
20080039830 Munger et al. Feb 2008 A1
20080051454 Wang Feb 2008 A1
20080064957 Spence Mar 2008 A1
20080071269 Hilario et al. Mar 2008 A1
20080071306 Gertner Mar 2008 A1
20080082109 Moll et al. Apr 2008 A1
20080086072 Bonutti et al. Apr 2008 A1
20080091193 Kauphusman et al. Apr 2008 A1
20080097251 Babaev Apr 2008 A1
20080097426 Root et al. Apr 2008 A1
20080108867 Zhou May 2008 A1
20080119879 Brenneman et al. May 2008 A1
20080125772 Stone et al. May 2008 A1
20080132450 Lee et al. Jun 2008 A1
20080140002 Ramzipoor et al. Jun 2008 A1
20080147002 Gertner Jun 2008 A1
20080161662 Golijanin et al. Jul 2008 A1
20080161717 Gertner Jul 2008 A1
20080161801 Steinke et al. Jul 2008 A1
20080171974 Lafontaine et al. Jul 2008 A1
20080172035 Starksen et al. Jul 2008 A1
20080172104 Kieval et al. Jul 2008 A1
20080188912 Stone et al. Aug 2008 A1
20080188913 Stone et al. Aug 2008 A1
20080208162 Joshi Aug 2008 A1
20080208169 Boyle et al. Aug 2008 A1
20080213331 Gelfand et al. Sep 2008 A1
20080215117 Gross Sep 2008 A1
20080221448 Khuri-Yakub et al. Sep 2008 A1
20080234790 Bayer et al. Sep 2008 A1
20080243091 Humphreys et al. Oct 2008 A1
20080245371 Gruber Oct 2008 A1
20080249525 Lee et al. Oct 2008 A1
20080249547 Dunn Oct 2008 A1
20080255550 Bell Oct 2008 A1
20080255642 Zarins et al. Oct 2008 A1
20080262489 Steinke Oct 2008 A1
20080275484 Gertner Nov 2008 A1
20080281312 Werneth et al. Nov 2008 A1
20080281347 Gertner Nov 2008 A1
20080287918 Rosenman et al. Nov 2008 A1
20080294037 Richter Nov 2008 A1
20080300618 Gertner Dec 2008 A1
20080312644 Fourkas et al. Dec 2008 A1
20080312673 Viswanathan et al. Dec 2008 A1
20080317818 Griffith et al. Dec 2008 A1
20090018486 Goren et al. Jan 2009 A1
20090018609 DiLorenzo Jan 2009 A1
20090024194 Arcot-Krishnamurthy et al. Jan 2009 A1
20090030312 Hadjicostis Jan 2009 A1
20090036948 Levin et al. Feb 2009 A1
20090043372 Northrop et al. Feb 2009 A1
20090054082 Kim et al. Feb 2009 A1
20090062873 Wu et al. Mar 2009 A1
20090069671 Anderson Mar 2009 A1
20090074828 Alexis et al. Mar 2009 A1
20090076409 Wu et al. Mar 2009 A1
20090088735 Abboud et al. Apr 2009 A1
20090105631 Kieval Apr 2009 A1
20090112202 Young Apr 2009 A1
20090118620 Tgavalekos et al. May 2009 A1
20090118726 Auth et al. May 2009 A1
20090125099 Weber et al. May 2009 A1
20090131798 Minar et al. May 2009 A1
20090143640 Saadat et al. Jun 2009 A1
20090156988 Ferren et al. Jun 2009 A1
20090157057 Ferren et al. Jun 2009 A1
20090157161 Desai et al. Jun 2009 A1
20090171333 Hon Jul 2009 A1
20090192558 Whitehurst et al. Jul 2009 A1
20090198223 Thilwind et al. Aug 2009 A1
20090203962 Miller et al. Aug 2009 A1
20090203993 Mangat et al. Aug 2009 A1
20090204170 Hastings et al. Aug 2009 A1
20090210953 Moyer et al. Aug 2009 A1
20090216317 Cromack et al. Aug 2009 A1
20090221955 Babaev Sep 2009 A1
20090226429 Salcedo et al. Sep 2009 A1
20090240249 Chan et al. Sep 2009 A1
20090247933 Maor et al. Oct 2009 A1
20090247966 Gunn et al. Oct 2009 A1
20090248012 Maor et al. Oct 2009 A1
20090253974 Rahme Oct 2009 A1
20090264755 Chen et al. Oct 2009 A1
20090270850 Zhou et al. Oct 2009 A1
20090281533 Ingle et al. Nov 2009 A1
20090287137 Crowley Nov 2009 A1
20090318749 Stolen et al. Dec 2009 A1
20100009267 Chase et al. Jan 2010 A1
20100030061 Canfield et al. Feb 2010 A1
20100048983 Ball et al. Feb 2010 A1
20100049099 Thapliyal et al. Feb 2010 A1
20100049186 Ingle et al. Feb 2010 A1
20100049188 Nelson et al. Feb 2010 A1
20100049191 Habib et al. Feb 2010 A1
20100049283 Johnson Feb 2010 A1
20100069837 Rassat et al. Mar 2010 A1
20100076299 Gustus et al. Mar 2010 A1
20100076425 Carroux Mar 2010 A1
20100087782 Ghaffari et al. Apr 2010 A1
20100106005 Karczmar et al. Apr 2010 A1
20100114244 Manda et al. May 2010 A1
20100125239 Perry et al. May 2010 A1
20100125268 Gustus et al. May 2010 A1
20100130836 Malchano et al. May 2010 A1
20100137860 Demarais et al. Jun 2010 A1
20100137952 Demarais et al. Jun 2010 A1
20100160903 Krespi Jun 2010 A1
20100160906 Jarrard Jun 2010 A1
20100168624 Sliwa Jul 2010 A1
20100168731 Wu et al. Jul 2010 A1
20100168739 Wu et al. Jul 2010 A1
20100174282 Demarais et al. Jul 2010 A1
20100191112 Demarais et al. Jul 2010 A1
20100191232 Boveda Jul 2010 A1
20100204560 Salahieh et al. Aug 2010 A1
20100217162 Hissong et al. Aug 2010 A1
20100222786 Kassab Sep 2010 A1
20100222851 Deem et al. Sep 2010 A1
20100222854 Demarais et al. Sep 2010 A1
20100228122 Keenan et al. Sep 2010 A1
20100249604 Hastings et al. Sep 2010 A1
20100249702 Magana et al. Sep 2010 A1
20100249773 Clark et al. Sep 2010 A1
20100256616 Katoh et al. Oct 2010 A1
20100268217 Habib Oct 2010 A1
20100268307 Demarais et al. Oct 2010 A1
20100284927 Lu et al. Nov 2010 A1
20100286684 Hata et al. Nov 2010 A1
20100298821 Garbagnati Nov 2010 A1
20100305036 Barnes et al. Dec 2010 A1
20100312141 Keast et al. Dec 2010 A1
20100324472 Wulfman Dec 2010 A1
20110009750 Taylor et al. Jan 2011 A1
20110021976 Li et al. Jan 2011 A1
20110034832 Cioanta et al. Feb 2011 A1
20110040324 McCarthy et al. Feb 2011 A1
20110044942 Puri et al. Feb 2011 A1
20110060324 Wu et al. Mar 2011 A1
20110071400 Hastings et al. Mar 2011 A1
20110071401 Hastings et al. Mar 2011 A1
20110077498 McDaniel Mar 2011 A1
20110092781 Gertner Apr 2011 A1
20110092880 Gertner Apr 2011 A1
20110104061 Seward May 2011 A1
20110112400 Emery et al. May 2011 A1
20110118598 Gertner May 2011 A1
20110118600 Gertner May 2011 A1
20110118726 De La Rama et al. May 2011 A1
20110130708 Perry et al. Jun 2011 A1
20110137155 Weber et al. Jun 2011 A1
20110144479 Hastings et al. Jun 2011 A1
20110146673 Keast et al. Jun 2011 A1
20110166499 Demarais et al. Jul 2011 A1
20110178403 Weng et al. Jul 2011 A1
20110178570 Demarais Jul 2011 A1
20110200171 Beetel et al. Aug 2011 A1
20110202098 Demarais et al. Aug 2011 A1
20110207758 Sobotka et al. Aug 2011 A1
20110208096 Demarais et al. Aug 2011 A1
20110257523 Hastings et al. Oct 2011 A1
20110257564 Demarais et al. Oct 2011 A1
20110257622 Salahieh et al. Oct 2011 A1
20110257641 Hastings et al. Oct 2011 A1
20110257642 Griggs, III Oct 2011 A1
20110263921 Vrba et al. Oct 2011 A1
20110264011 Wu et al. Oct 2011 A1
20110264075 Leung et al. Oct 2011 A1
20110264086 Ingle Oct 2011 A1
20110264116 Kocur et al. Oct 2011 A1
20110270238 Rizq et al. Nov 2011 A1
20110306851 Wang Dec 2011 A1
20110307034 Hastings et al. Dec 2011 A1
20110319809 Smith Dec 2011 A1
20120029496 Smith Feb 2012 A1
20120029500 Jenson Feb 2012 A1
20120029505 Jenson Feb 2012 A1
20120029509 Smith Feb 2012 A1
20120029510 Haverkost Feb 2012 A1
20120029511 Smith et al. Feb 2012 A1
20120029512 Willard et al. Feb 2012 A1
20120029513 Smith et al. Feb 2012 A1
20120059241 Hastings et al. Mar 2012 A1
20120059286 Hastings et al. Mar 2012 A1
20120065506 Smith Mar 2012 A1
20120065554 Pikus Mar 2012 A1
20120095461 Herscher et al. Apr 2012 A1
20120101413 Beetel et al. Apr 2012 A1
20120101490 Smith Apr 2012 A1
20120101538 Ballakur et al. Apr 2012 A1
20120109021 Hastings et al. May 2012 A1
20120116382 Ku et al. May 2012 A1
20120116383 Mauch et al. May 2012 A1
20120116392 Willard May 2012 A1
20120116438 Salahieh et al. May 2012 A1
20120116486 Naga et al. May 2012 A1
20120123243 Hastings May 2012 A1
20120123258 Willard May 2012 A1
20120123261 Jenson et al. May 2012 A1
20120123303 Sogard et al. May 2012 A1
20120123406 Edmunds et al. May 2012 A1
20120130289 Demarais et al. May 2012 A1
20120130345 Levin et al. May 2012 A1
20120130359 Turovskiy May 2012 A1
20120130360 Buckley et al. May 2012 A1
20120130362 Hastings et al. May 2012 A1
20120130368 Jenson May 2012 A1
20120130458 Ryba et al. May 2012 A1
20120136344 Buckley et al. May 2012 A1
20120136349 Hastings May 2012 A1
20120136350 Goshgarian et al. May 2012 A1
20120136417 Buckley et al. May 2012 A1
20120136418 Buckley et al. May 2012 A1
20120143181 Demarais et al. Jun 2012 A1
20120143293 Mauch et al. Jun 2012 A1
20120143294 Clark et al. Jun 2012 A1
20120150267 Buckley et al. Jun 2012 A1
20120157986 Stone et al. Jun 2012 A1
20120157987 Steinke et al. Jun 2012 A1
20120157988 Stone et al. Jun 2012 A1
20120157989 Stone et al. Jun 2012 A1
20120157992 Smith et al. Jun 2012 A1
20120157993 Jenson et al. Jun 2012 A1
20120158101 Stone et al. Jun 2012 A1
20120158104 Huynh et al. Jun 2012 A1
20120172837 Demarais et al. Jul 2012 A1
20120172870 Jenson et al. Jul 2012 A1
20120184952 Jenson et al. Jul 2012 A1
20120197198 Demarais et al. Aug 2012 A1
20120197252 Deem et al. Aug 2012 A1
20120232409 Stahmann et al. Sep 2012 A1
20120265066 Crow et al. Oct 2012 A1
20120265198 Crow et al. Oct 2012 A1
20130012844 Demarais et al. Jan 2013 A1
20130012866 Deem et al. Jan 2013 A1
20130012867 Demarais et al. Jan 2013 A1
20130013024 Levin et al. Jan 2013 A1
20130023865 Steinke et al. Jan 2013 A1
20130035681 Subramanaim et al. Feb 2013 A1
20130066316 Steinke et al. Mar 2013 A1
20130085489 Fain et al. Apr 2013 A1
20130090563 Weber Apr 2013 A1
20130090578 Smith et al. Apr 2013 A1
20130090647 Smith Apr 2013 A1
20130090649 Smith et al. Apr 2013 A1
20130090650 Jenson et al. Apr 2013 A1
20130090651 Smith Apr 2013 A1
20130090652 Jenson Apr 2013 A1
20130096550 Hill Apr 2013 A1
20130096553 Hill et al. Apr 2013 A1
20130096554 Groff et al. Apr 2013 A1
20130096604 Hanson et al. Apr 2013 A1
20130110106 Richardson May 2013 A1
20130116687 Willard May 2013 A1
20130165764 Scheuermann et al. Jun 2013 A1
20130165844 Shuros et al. Jun 2013 A1
20130165916 Mathur et al. Jun 2013 A1
20130165917 Mathur et al. Jun 2013 A1
20130165920 Weber et al. Jun 2013 A1
20130165923 Mathur et al. Jun 2013 A1
20130165924 Mathur et al. Jun 2013 A1
20130165925 Mathur et al. Jun 2013 A1
20130165926 Mathur et al. Jun 2013 A1
20130165990 Mathur et al. Jun 2013 A1
20130172815 Perry et al. Jul 2013 A1
20130172872 Subramaniam et al. Jul 2013 A1
20130172877 Subramaniam et al. Jul 2013 A1
20130172878 Smith Jul 2013 A1
20130172879 Sutermeister Jul 2013 A1
20130172880 Willard Jul 2013 A1
20130172881 Hill et al. Jul 2013 A1
Foreign Referenced Citations (162)
Number Date Country
2384866 Apr 2001 CA
10038737 Feb 2002 DE
102005041601 Apr 2007 DE
102008048616 Apr 2010 DE
0558297 Sep 1993 EP
0647435 Apr 1995 EP
0634910 Aug 1997 EP
0868884 Oct 1998 EP
1005838 Jun 2000 EP
1053720 Nov 2000 EP
1064886 Jan 2001 EP
1180004 Feb 2002 EP
1181895 Feb 2002 EP
1264613 Dec 2002 EP
1297795 Apr 2003 EP
1286625 May 2003 EP
1332724 Aug 2003 EP
1335677 Aug 2003 EP
0866675 Oct 2003 EP
1433448 Jun 2004 EP
1442719 Aug 2004 EP
1547537 Jun 2005 EP
1634542 Mar 2006 EP
1698296 Sep 2006 EP
1709922 Oct 2006 EP
1874211 Jan 2008 EP
1906853 Apr 2008 EP
1946712 Jul 2008 EP
1961394 Aug 2008 EP
1715798 Apr 2009 EP
1620156 Jul 2009 EP
2076193 Jul 2009 EP
2091455 Aug 2009 EP
2197533 Jun 2010 EP
2208506 Jul 2010 EP
1579889 Aug 2010 EP
2241279 Oct 2010 EP
2092957 Jan 2011 EP
2239859 Jun 2011 EP
2329859 Jun 2011 EP
2349044 Aug 2011 EP
2027882 Oct 2011 EP
2378956 Oct 2011 EP
2037840 Dec 2011 EP
2204134 Apr 2012 EP
2320821 Oct 2012 EP
2313062 Nov 1997 GB
2453601 Apr 2009 GB
2456301 Jul 2009 GB
7213621 Aug 1995 JP
7313603 Dec 1995 JP
2003510126 Mar 2003 JP
9103207 Mar 1991 WO
9117731 Nov 1991 WO
9222239 Dec 1992 WO
9320747 Oct 1993 WO
9320770 Oct 1993 WO
9418896 Sep 1994 WO
9428809 Dec 1994 WO
9501751 Jan 1995 WO
9531142 Nov 1995 WO
9634559 Nov 1996 WO
9703604 Feb 1997 WO
9717104 May 1997 WO
9720510 Jun 1997 WO
9732532 Sep 1997 WO
9740760 Nov 1997 WO
9745156 Dec 1997 WO
9745157 Dec 1997 WO
9818393 May 1998 WO
9829030 Jul 1998 WO
9834565 Aug 1998 WO
9835638 Aug 1998 WO
9840023 Sep 1998 WO
9858588 Dec 1998 WO
9900060 Jan 1999 WO
9916370 Apr 1999 WO
9921608 May 1999 WO
9934741 Jul 1999 WO
9944522 Sep 1999 WO
0001313 Jan 2000 WO
0010475 Mar 2000 WO
0047118 Aug 2000 WO
0051513 Sep 2000 WO
0059394 Oct 2000 WO
0062727 Oct 2000 WO
0064387 Nov 2000 WO
0069376 Nov 2000 WO
0072909 Dec 2000 WO
0122897 Apr 2001 WO
0137746 May 2001 WO
0174255 Oct 2001 WO
0137723 Nov 2001 WO
0187154 Nov 2001 WO
0187172 Nov 2001 WO
0195820 Dec 2001 WO
0215807 Feb 2002 WO
0228475 Apr 2002 WO
0239915 May 2002 WO
02058549 Aug 2002 WO
02080766 Oct 2002 WO
02087679 Nov 2002 WO
02089686 Nov 2002 WO
02089871 Nov 2002 WO
03026525 Apr 2003 WO
03077781 Sep 2003 WO
2004047659 Jun 2004 WO
2004049976 Jun 2004 WO
2004064606 Aug 2004 WO
2004069300 Aug 2004 WO
2004076146 Sep 2004 WO
2004098694 Nov 2004 WO
2004100813 Nov 2004 WO
2004105807 Dec 2004 WO
2004110258 Dec 2004 WO
2005007000 Jan 2005 WO
2005037070 Apr 2005 WO
2005041748 May 2005 WO
2005074829 Aug 2005 WO
2006041881 Apr 2006 WO
2006105121 Oct 2006 WO
2006116198 Nov 2006 WO
2007011634 Jan 2007 WO
2007014063 Feb 2007 WO
2007047870 Apr 2007 WO
2007113865 Oct 2007 WO
2007135431 Nov 2007 WO
2007146215 Dec 2007 WO
2008003058 Jan 2008 WO
2008009972 Jan 2008 WO
2008010150 Jan 2008 WO
2008014465 Jan 2008 WO
2008036281 Mar 2008 WO
2008049084 Apr 2008 WO
2008061152 May 2008 WO
2008102363 Aug 2008 WO
2009036471 Mar 2009 WO
2009082635 Jul 2009 WO
2009088678 Jul 2009 WO
2009113064 Sep 2009 WO
2009121017 Oct 2009 WO
2009137819 Nov 2009 WO
2010042653 Apr 2010 WO
2010048007 Apr 2010 WO
2010056771 May 2010 WO
2010057043 May 2010 WO
2010067360 Jun 2010 WO
2010070766 Jun 2010 WO
2010099207 Sep 2010 WO
2010102310 Sep 2010 WO
2010120944 Oct 2010 WO
2010134503 Nov 2010 WO
2011005901 Jan 2011 WO
2011053757 May 2011 WO
2011053772 May 2011 WO
2011055143 May 2011 WO
2011060339 May 2011 WO
2011091069 Jul 2011 WO
2011126580 Oct 2011 WO
2011130534 Oct 2011 WO
2012019156 Feb 2012 WO
2013049601 Apr 2013 WO
Non-Patent Literature Citations (70)
Entry
CardioVascular Technologies Inc., “Heated Balloon Device Technology,” 11 pages, 2008.
Strategic Business Development, Inc., “Thermal and Disruptive Angioplasty: A Physician's Guide,” 8 pages, 1990.
Zhang et al., “Non-contact Radio-Frequency Ablation for Obtaining Deeper Lesions,” IEEE Transaction on Biomedical Engineering, vol. 50, No. 2, 6 pages, Feb. 2003.
Lazebnik et al., “Tissue Strain Analytics Virtual Touch Tissue Imaging and Qualification,” Siemens Whitepaper, Oct. 2008, 7 pages.
Zhou et al., “Mechanism Research of Cryoanalgesia,” Forefront Publishing Group, 1995.
Florete, “Cryoblative Procedure for Back Pain,” Jacksonville Medicine, Oct. 1998, 10 pages.
Stevenson, “Irrigated RF Ablation: Power Titration and Fluid Management for Optimal Safety Efficacy,” 2005, 4 pages.
Giliatt et al., “The Cause of Nerve Damage in Acute Compression,” Trans Am Neurol Assoc, 1974: 99; 71-4.
Baun, “Interaction with Soft Tissue,” Principles of General & Vascular Sonography, Chapter 2, pp. 23-24, Before Mar. 2012.
Blue Cross Blue Shield Medicaly Policy, “Surgery Section—MRI-Guided Focused Ultrasound (MRgFUS) for the Treatment of Uterine Fibroids and Other Tumors,” 2005, 5 pages.
Gentry et al., “Combines 3D Intracardiac Echo and Ultrasound Ablation,” Medical Imaging 2003: Ultrasonic and Signal Processing, vol. 5035, 2003, pp. 166-173.
Lafon et al., “Optmizing the Shape of Ultrasound Transducers for Interstitial Thermal Ablations,” MEd Phys. Mar. 2002; 29(3): 290-7 (abstract only).
G. Ter Haar, “Ultrasound Focal Beam Surgery,” Ultrasound in Med. & Biol., 1995, vol. 21, No. 9, pp. 1089-1100.
Seip et al., “Transurethral High Intensity Focused Ultrasound: Catheter Based Prototypes and Experimental Results,” IEEE Ultrasonics Symposium Proceeding, 2000, 4 pages.
Toytman et al., “Tissue Dissection with Ultrafast Laser Using Extended and Multiple Foci,” SPIE Proceeding, Optical Interactions with Tissues and Cells XXI, vol. 7562, 2010, 10 pages.
Zhoue et al., “Non-Thermal Ablation of Rabbit Liver VX2 Tumore by Pulsed High Intensity Focused Ultrasound Contrast Agent: Pathological Characteristics,” World Journal of Gastroenterology, vol. 14(43), Nov. 21, 2008, pp. 6743-6747.
US 8,398,630, 3/2013, Demarais et al (withdrawn).
Van Den Berg, “Light echoes image the human body,” OLE, Oct. 2001, p. 35-37.
“IntraLuminal: Products,” IntraLuminal Therapeutics, Inc., 2003, p. 1-9.
“Laser Catheter to Aid Coronary Surgery,” TechTalk: MIT, Jan. 9, 1991, p. 1-4.
“Optical Coherence Tomography: LightLab Imaging Starts US Cardiology Clinical Investigations,” LightLab Imaging Technology, 2002.
“Optical Coherence Tomography: LightLab Sees Bright Prospects for Cardiac Application of OCT Technology,” LightLab Imaging Technology, 2001, vol. 27, No. 35.
“Products—Functional Measurement,” VOLCANO Functional Measurement Products US, Mar. 24, 2003, p. 1-2.
Brown et al., “Radiofrequency capacitive heaters: the effect of coupling medium resistivity on power absorption along a mouse leg,” Physics in Medicine and Biology, 1993, p. 1-12, vol. 38.
Carrington, “Future of CVI: It's all about plaque: Identification of vulnerable lesions, not ‘rusty pipes,’ could become cornerstone of preventive cardiology,” Diagnostic Imaging, 2001, p. 1-8.
Chen et al., “Percutaneous pulmonary artery denervation completely abolishes experimental pulmonary arterial hypertension in vivo,” EuroIntervention, 2013, p. 1-8.
Cimino, “Preventing plaque attack,” Mass High Tech, 2001, p. 1-2.
Dahm et al., “Relation of Degree of Laser Debulking of In-Stent Restenosis as a Predictor of Restenosis Rate,” The American Journal of Cardiology, 2002, p. 68-70, vol. 90.
De Korte et al., “Characterization of Plaque Components With Intravascular Ultrasound Elastography in Human Femoral and Coronary Arteries In Vitro,” Circulation, Aug. 8, 2000, p. 617-623.
Durney et al., “Radiofrequency Radiation Dosimetry Handbook,” Oct. 1986, p. 1-2, Fourth Edition.
Durney et al., “Radiofrequency Radiation Dosimetry Handbook: Contents,” Oct. 1986, p. 1-5, Fourth Edition.
Fournier-Desseux et al., “Assessment of 1-lead and 2-lead electrode patterns in electrical impedance endotomography,” Physiological Measurement, 2005, p. 337-349. Vo. 26, Institute of Physics Publishing.
Fram et al., “Feasibility of Radiofrequency Powered, Thermal Balloon Ablation of Atrioventricular Bypass Tracts via the Coronary Sinus: In Vivo Canine Studies,” PACE, Aug. 1995, p. 1518-1530, vol. 18.
Fram et al., “Low Pressure Radiofrequency Balloon Angioplasty: Evaluation in Porcine Peripheral Arteries,” JACC, 1993, p. 1512-1521, vol. 21, No. 6, American College of Cardiology.
Fujimori et al., “Significant Prevention of In-Stent Restenosis by Evans Blue in Patients with Acute Myocardial Infarction,” American Heart Association, 2002.
Fujita et al., “Sarpogrelate, An Antagonist of 5-HT(2A) Receptor, Treatment Reduces Restenosis After Coronary Stenting,” American Heart Association, 2002.
Gabriel, “Appendix A: Experimental Data,” 1999, p. 1-21.
Gregory et al., “Liquid Core Light Guide for Laser Angioplasty,” The Journal of Quantum Electronics, Dec. 1990, p. 2289-2296, vol. 26, No. 12.
Kaplan et al., “Healing after Arterial Dilatation with Radiofrequency Thermal and Nonthermal Balloon Angioplasty Sytems,” Journal of Investigative Surgery, 1993, p. 33-52, vol. 6.
Kolata, “New Studies Question Value of Opening Arteries,” The New York Times, Mar. 21, 2004, p. 1-5.
Konings et al., “Development of an Intravascular Impedance Catheter for Detection of Fatty Lesions in Arteries,” IEEE Transactions on Medical Imaging, Aug. 1997, p. 439-446, vol. 16, No. 4.
Kurtz et al., “Lamellar Refractive Surgery with Scanned Intrastromal Picosecond and Femtosecond Laser Pulses in Animal Eyes,” Journal of Refractive Surgery, Sep./Oct. 1998, p. 541-548.
Lee et al., “Thermal Compression and Molding of Atherosclerotic Vascular Tissue With Use of Radiofrequency Energy: Implications for Radiofrequency Balloon Angioplasty,” JACC, 1989, p. 1167-1175, vol. 13, No. 5, American College of Cardiology.
Lima et al., “Efficacy and Safety of Oral Sirolimus to Treat and Prevent In-Stent Restenosis: A Pilot Study Results,” American Heart Association, 2002, p. 2929.
Lima et al., “Systemic Immunosuppression Inhibits In-Stent Coronary Intimal Proliferation in Renal Transplant Patients,” American Heart Association, 2002, p. 2928.
Morice et al., “A Randomized Comparison of a Sirolimus-Eluting Stent With a Standard Stent for Coronary Revascularization,” The New England Journal of Medicine, Jun. 6, 2012, p. 1773-1780, vol. 346, No. 23.
Muller-Leisse et al., “Effectiveness and Safety of Ultrasonic Atherosclerotic Plaque Ablation: In Vitro Investigation,” CardioVascular and Interventional Radiology, 1993, p. 303-307, vol. 16.
Nair et al., “Regularized Autoregressive Analysis of Intravascular Ultrasound Backscatter: Improvement in Spatial Accuracy of Tissue Maps,” IEEE Transactions on Ultrasonics, Apr. 2004, p. 420-431, vol. 51, No. 4.
Resar et al., “Endoluminal Sealing of Vascular Wall Disruptions With Radiofrequency-Heated Balloon Angioplasty,” Catheterization and Cardiovascular Diagnosis, 1993, p. 161-167, vol. 29.
Romer et al., “Histopathology of Human Coronary Atherosclerosis by Quantifying Its Chemical Composition With Raman Spectroscopy,” Circulation, 1998, p. 878-885, vol. 97.
Schauerte et al., “Catheter Ablation of Cardiac Autonomic Nerves for Prevention of Vagal Atrial Fibrillation,” Circulation, 2000, p. 2774-2780, vol. 102.
Scheller et al., “Intracoronary Paclitaxel Added to Contrast Media Inhibits In-Stent Restenosis of Porcine Coronary Arteries,” American Heart Association, 2002, p. 2227.
Scheller et al., “Potential solutions to the current problem: coated balloon,” EuroIntervention, 2008, p. C63-C66, vol. 4 (Supplement C).
Shaffer, “Scientific basis of laser energy,” Clinics in Sports Medicine, 2002, p. 585-598, vol. 21.
Shmatukha et al., “MRI temperature mapping during thermal balloon angioplasty,” Physics in Medicine and Biology, 2006, p. N163-N171, vol. 51.
Slager et al., “Vaporization of Atherosclerotic Plaques by Spark Erosion,” J Am Coll Cardiol, 1985, p. 21-25.
Stiles et al., “Simulated Characterization of Atherosclerotic Lesions in the Coronary Arteries by Measurement of Bioimpedance,” IEEE Transactions on Biomedical Engineering, Jul. 2003, p. 916-921, vol. 50, No. 7.
Suselbeck et al., “In vivo intravascular electric impedance spectroscopy using a new catheter with integrated microelectrodes,” Basic Res Cardiol, 2005, p. 28-34, vol. 100.
Suselbeck et al., “Intravascular electric impedance spectroscopy of atherosclerotic lesions using a new impedance catheter system,” Basic Res Cardiol, 2005, p. 446-452, vol. 100.
Tepe et al., “Local Delivery of Paclitaxel to Inhibit Restenosis during Angioplasty of the Leg,” The New England Journal of Medicine, 2008, p. 689-699, vol. 358.
Brown et al., “Observations on the Shrink Temperature of Collagen and Its Variations with Age and Disease,” Ann Rheum Dis., vol. 17, No. 2, pp. 196-208, Jun. 1, 1958.
Gabriel C, et al., Compilation of the Dielectric Properties of Body Tissues at RF and Microwave Frequencies (with table of contents), Jun. 1996, 17 pages, Armstrong Laboratory (AFMC) Occupational and Environmental Health Directorate Radiofrequency Radiation Division, USAF School of Aerospace Medicine, Aerospace Medical Division (AFSC), Brooks Air Force Base, http://www.brooks.af.mil/AFRL/HED/hedr/reports/dielectric/Report/Report.html.
Gabriel, “Appendix C: Modeling the frequency dependence of the dielectric properties to a 4 dispersions spectrum,” p. 1-49, Nov. 6, 1997.
Han et al., “Third-Generation Cryosurgery for Primary and Recurrent Prostate Caner,” BJU International, vol. 93, pp. 14-18, 2004.
Omura et al., “A Mild Acute Compression Induces Neurapraxia in Rat Sciatic Nerve,” The International Journal of Neuroscience, vol. 114 (12), pp. 1561-1572, Dec. 2004.
“Optical Coherence Tomography: Advantages of OCT,” LightLab Imaging Technology, printed Sep. 3, 2003.
“Optical Coherence Tomography: Image Gallery Cardiovascular Procedures,” LightLab Imaging Technology, printed Sep. 3, 2003.
“Optical Coherence Tomography: What is OCT?,” LightLab Imaging Technology, printed Sep. 3, 2003.
“Optical Coherence Tomography: Why Use OCT?,” LightLab Imaging Technology, printed Sep. 3, 2003.
Popma et al., “Percutaneous Coronary and Valvular Intervention,” Braunwald's Heart Disease: A Textbook of Cardiovascular Medicine, 7th edition, p. 1364-1405, 2005.
Related Publications (1)
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20130066316 A1 Mar 2013 US
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Child 11864779 US
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Parent 13403920 Feb 2012 US
Child 13671474 US
Parent 11864779 Sep 2007 US
Child 13403920 US