Catheter for obstructed stent

Claim 3

The device of claim 1, wherein said first electrode is located on the interior surface of said elongate flexible tube, and said elongate tube has a lip extending distal to said first electrode.

Claim 4

The device of claim 2, further comprising a first plurality of electrodes on the interior of said elongate flexible tube proximate the distal end, said electrodes being circumferentially spaced about the interior of the tube; and the power supply allowing current to be selectively supplied to any of the plurality of electrodes.

Claim 5

The device of claim 3, further comprising a return electrode in electrical communication with the current supply, the return electrode being attachable to a patient.

Claim 6

The device of claim 3, further comprising means for visualizing the location of said distal end of said elongate tube and determining the composition and amount of the obstructive material.

Claim 7

The device of claim 5, wherein the means for visualizing include an ultrasound transducer.

Claim 8

The device of claim 5, wherein the means for visualizing include fiber optics.

Claim 9

The device of claim 5, wherein the means for visualizing include a fluoroscopic device.

Claim 10

The device of claim 1, wherein said tube has a groove proximate said distal end, said groove being formed within an exterior surface of said tube; said first electrode being situated within said groove; and said first electrode being sized so that it is recessed within the groove, whereby said electrode is unobstructed in the radial direction.

Claim 11

The device of claim 9, further comprising a return electrode located on said tube.

Claim 12

The device of claim 10, wherein said return electrode may be positioned so as to physically contact said stent.

Claim 13

The device of claim 1, further comprising a plurality of grooves within said tube, each of said grooves being formed within an exterior surface of said tube, and a plurality of electrodes, wherein at least one of said plurality of electrodes is recessed within each of said plurality of grooves, and whereby said electrodes are unobstructed in the radial direction.

Claim 14

The device of claim 1, further comprising a plurality of electrodes located on said tube, at least some of the plurality of electrodes being located further distal on the catheter than other of the plurality of electrodes; and the power supply allowing each of the plurality of electrodes to independently receive current.

Claim 15

The device of claim 13, wherein at least one of the plurality of electrodes may be alternately made a supply or return electrode by the current source.

Claim 16

The device of claim 13, further comprising means for sensing the impedance between at least two of said electrodes, the impedance sensing means detecting whether one or both of the at least two electrodes are within the stent so that only an electrode within the stent is suppled with ablative current.

Claim 17

The device of claim 15, further comprising spacers disposed about said tube proximate said electrodes, said spacers projecting radially further from the tube than said electrodes, said spacers projecting a distance sufficient to prevent said electrodes from contacting the stent.

Claim 18

The device of claim 16, wherein said plurality of electrodes are arranged in a series of rings located around said tube.

Claim 19

The device of claim 1 wherein the electrode directs current distal to the distal end of the device.

Claim 20

The device of claim 1, further comprising a second electrode, the second electrode projecting radially further from the axis of tube than the first electrode.

Claim 21

The device of claim 19, further comprising a first plurality of electrodes and a second plurality of electrodes; each of the first plurality of electrodes being shielded from contact with the stent when each of the first plurality of electrodes are positioned within the stent; and each of the second plurality of electrodes extending further from the tube axis than each of the first plurality of electrodes.

Claim 22

The device of claim 1, further comprising means for delivering bioactive fluid exterior to the tube.

Claim 23

The device of claim 21, further comprising means for delivering energy to increase the bioactivity of the fluid.

Claim 24

The device of claim 22, wherein the energy to increase the bioactivity of the fluid consists of electrical energy, optical energy, mechanical energy, or acoustical energy.

Claim 25

The device of claim 1, further comprising at least two sensing electrodes proximate the distal end, and means to sense the impedance between the sensing electrodes.

Claim 26

The device of claim of claim 1, further comprising insulating material that partially covers the electrode, said insulating material separating the electrode from the stent.

Claim 27

The device of claim 25, wherein the insulating material is perforated.

Claim 28

The device of claim 25, wherein the insulating material is cross hatched.

Claim 29

The device of claim 1, further comprising: a first plurality of electrodes including the first electrode, the first plurality of electrodes being disposed about the distal end of the catheter; a second plurality of electrodes, each of the second plurality of electrodes being disposed about the distal end of the catheter; the first plurality of electrodes being interspaced with the second plurality so that members of the first plurality alternate with members of the second plurality across a portion of the distal end of the catheter; and wherein the first plurality are electrically interconnected in parallel to a first polarity and the second plurality are electrically interconnected in parallel to an opposite polarity.

Claim 34

The method of claim 30, wherein the positioning step includes using visualization means to visualize the position of the distal end in relation to said stent.

Claim 35

The method of claim 30, wherein the visualization means include ultrasound transducers.

Claim 36

The method of claim 30, wherein the visualization means include fiber optics.

Claim 37

The method of claim 30, wherein said device contains at least two electrodes proximate said distal end, and the positioning step includes determining the position of the distal end in relation to the stent by establishing current flow between at least two of said electrodes and determining the impedance therebetween.

Claim 38

The method of claim 34, further comprising the step of establishing direct electrical communication between said stent and said current source.

Claim 39

The method of claim 30, further comprising the step of supplying bioactive fluid through the device to medicate said subject.

Claim 40

The method of claim 36, further comprising supplying energy to increase the bioactivity of the fluid.

Claim 41

The method of claim 37, wherein the energy to increase the bioactivity of the fluid consists of electrical energy, optical energy, mechanical energy, or acoustical energy.

Claim 42

The method of claim 30 further comprising the step of ablating material exterior to said stent, the step of ablating material exterior to said stent being performed by a second electrode.

Claim 43

The method of claim 30, wherein the positioning step includes measuring the impedance between at least two sensing electrodes located on said device.

Claim 44

A therapeutic method to increase flow through an at least partially obstructed lumen, comprising the steps of: deploying a stent with the abstract lumen; inserting an ablation device within the stent, the device having (a) an elongate flexible tube having a distal end and a proximal end and an interior surface therebetween, the tube defining an axial direction along a length of the tube and a radial direction radially away from the tube; (b) a first ablation electrode positioned within said interior surface proximate the distal end; (c) an ablation power supply in electrical communication with said ablation electrode; (d) wherein said first ablation electrode is shielded from physical contact with the stent by said tube when the first ablation electrode is positioned within the stent; and wherein said first ablation electrode is positioned so that it is electrically unobstructed in the radial direction by the tube while being shielded from physical contact with the stent, thereby being electrically operative in the radial direction with respect to its position along the axial direction; and using said ablation device to ablate obstructions from the stent.

Claim 45

A therapeutic method to increase flow through an at least partially obstructed lumen, comprising the steps of: deploying a stent with the abstract lumen; inserting an ablation device within the stent, the device having (a) an elongate flexible tube having a distal end and a proximal end and an interior surface therebetween, the tube defining an axial direction along a length of the tube and a radial direction radially away from the tube; (b) a first ablation electrode positioned within said interior surface proximate the distal end; (c) an ablation power supply in electrical communication with said ablation electrode; (d) wherein said first ablation electrode is shielded from physical contact with the stent by said tube when the first ablation electrode is positioned within the stent; and wherein said first ablation electrode is positioned so that it is electrically unobstructed in the radial direction by the tube while being shielded from physical contact with the stent, thereby being electrically operative in the radial direction with respect to its position along the axial direction; and using said ablation device to ablate obstructions from the stent.