Intraluminal electrode assembly

Description of equivalent WO 2006031899 A2

INTRALUMINAL ELECTRODE ASSEMBLY

0002CROSS-REFERENCE TO RELATED APPLICATIONS The present application claims priority to U.S. Provisional Application No. 60/608,513, filed on September 10, 2004, which is incorporated by reference herein.

FIELD OF THE INVENTION

0004The present invention is directed to an expandable intraluminal electrode assembly.

BACKGROUND OF THE INVENTION

0006Neuromodulation, which involves delivering electrical impulses to neural target sites, has become an important therapeutic method and is an option when other forms of treatment, such as drug administration, are ineffective. Neuromodulation has revolutionized the treatment of several neurological disorders, such as movement disorders and chronic pain and has been described in U.S. Patent No. 6885,888 for treating heart contractility. Technical and mechanical limitations, however, create obstacles to the final application of such methods in patients. For example, one obstacle is in the invasive nature of neuromodulation, which requires open surgery.

0007As such, there is a need for further approaches for neuromodulation, particularly minimally invasive approaches.

0008SUMMARY OF THE INVENTION hi an embodiment, the present invention provides an intraluminal electrode assembly comprising a cannulated tube and a plurality of wires disposed in the cannulated tube. Each of the plurality of wires has one of a plurality of electrical contacts at a distal end thereof. The plurality of wir^ps assumes a radially constrgined configuration within the cannulated tube in a retracted position and a radially extended configuration outward of the cannulated tube in a deployed position. The electrode assembly further comprises a spring wire connecting the plurality of electrical contacts together to collectively form a substantially circular configuration in a deployed position. BRIEF DESCRIPTION OF THE DRAWINGS

0009The present invention will become more fully understood from the detailed description given hereinbelow and the accompanying drawings which are given by way of illustration only. It should be understood that the present invention is in no way limited to the particular arrangement or inclusion of components depicted in the accompanying drawings and wherein:

0010FIG. 1 depicts a perspective view of an embodiment of an intraluminal electrode assembly according to the present invention in a retracted position.

0011FIG. 2 depicts a perspective view of an embodiment of an intraluminal electrode assembly according to the present invention in a deployed position.

0012FIG. 3 depicts an end view of an embodiment of an intraluminal electrode assembly according to the present invention.

0013FIG. 4 depicts a pulmonary artery catheter including an embodiment of an intraluminal electrode assembly according to the present invention.

0014FIG. 5 illustrates a step from an exemplary method of delivering a pulmonary artery catheter including an embodiment of an intraluminal electrode assembly according to the present invention.

0015FIG. 6 illustrates a step after the step illustrated in FIG. 5 from an exemplary method of delivering a pulmonary artery catheter including an embodiment of an intraluminal electrode assembly according to the present invention.

DETAILED DESCRIPTION OF THE INVENTION

0017Referring to FIGs. 1-3, the present invention provides an electrode assembly 10 comprising a cannulated tube 20, which can be a catheter, housing a plurality of wires 30. Each of the plurality of wires 30 has one of a plurality of electrical contacts 40 at a distal end thereof. Referring specifically to FIG. 1, in a retracted position, the plurality of wires 30 assumes a radially constrained configuration within cannulated tube 20. Referring to FIG. 2, in a deployed position, the distal portion of plurality of wires 30 assumes a radially extended configuration outward of cannulated tube 20. As seen from the end view of electrode assembly 10 in FIG. 3, a spring wire 50 connects the plurality of electrical contacts 40 (depicted as electrical contacts 40a-40g) together to form a substantially circular configuration in a deployed position. Ih an embodiment, plurality of wires 30, or at least the distal portion of plurality of wires 30 having electrical contacts 40 are fabricated from a shape memory material to allow the distal portion to project concentrically out of cannulated tube 20. Of course, other mechanisms for allowing the distal portion of plurality of wires 30 having electrical contacts 40 to project radially outward from cannulated tube 20 can be employed.

0018Although electrode assembly 10 is not necessarily limited to any particular use, the substantially circular configuration of the distal end of deployed plurality of wires 30 allows electrode assembly 10 to be used for intraluminal purposes, such as transvascular electrical neuromodulation of a target site adjacent to a vessel. Specifically, referring to FIG. 1, electrode assembly 10 can be inserted into a vessel 60 and urged distally forward. Referring to FIG. 2, upon reaching the desired point in vessel 60, plurality of wires 30 can be deployed to project radially outward to reach and contact the walls of vessel 60. Since all the plurality of wires 30 have the same shape, the final resulting vector drives the distal portion of plurality of wires 30 out from cannulated tube 20 to contact the wall of vessel 60.

0019In a preferred embodiment, plurality of wires 30 comprises six to eight wires. Further preferably, each of the plurality of electrical contacts 40 of the plurality of wires 30 can be selectively activated such that select electrical contacts 40 on one segment of the arc of the distal end of the plurality of wires 30 can be activated to apply focused electrical signals on a desired side of a vessel. The selective powerability over each electrical contact 40 may be achieved by employing a system including a programmer coupled via a conductor to a telemetry antenna. The programmer is capable of sending signals via the telemetry antenna to control the electrical signal delivered to electrical contacts 40. Such a system permits the selection of various pulse output options after electrode assembly 10 is positioned using telemetry communications. The present, invention als^~o contemplated radio-frequency systems to selectively power electrical contacts 40.

0020As will be understood by one of skill in the art, the independent powerability of electrical contacts 40 also provides a practitioner with a means of modify or steering the direction and locus of application of electrical signals to precisely target portions of the target region to achieve the desired therapy. For example, with reference to FIG. 2, electrical contact 40a may be powered to apply an electrical signal to an area adjacent thereto while the signal to electrical contact 4Oe may be substantially minimized to reduce or stop the application of an electrical signal to an area adjacent to electrical contact 4Oe. Because the locus of stimulation can be selectively adjusted and/or steered in this embodiment of electrode assembly 10, specific areas of the target region can be precisely targeted to achieve the desired therapy. Other or additional means of selectively steering the application of electrical signals may also be utilized in the present invention, such as the methods described in U.S. Patent No. 5,713,922, which is incorporated by reference herein.

0021Referring to FIG. 2, in a preferred embodiment, the proximal end of each of the plurality of wires 30 is in communication with rotator 70 at the proximal end of cannulated tube 20 such the distal end of the plurality of wires 30 can be rotated by similar motion of rotator 70. For example, rotator 70 could be a rotary motor or a manual dial that transfers rotational motion from rotator 70 to the distal end of the plurality of wires 30.

0022The present invention also provides an electrode assembly system including electrode assembly 10 and further including components useful in identifying, monitoring, or affecting a target region. For example, such a system could include a component for lesioning and temperature monitoring, and/or a component that has a fiberoptic monitor which allows telemetric intracranial monitoring capabilities, and/or a microelectrode recording component, and/or a sensing component to incorporate a feedback mechanism to assist in determining whether electrical contacts 40 should be adjusted. With respect to a sensing component, a sensor can be incorporated with the electrode assembly system according to the present invention. The sensors can be used with a closed-loop feedback system in order to automatically determine the level of electrical signal to apply to provide the desired therapy. The sensors may be implanted or positioned in or at a portion of the patient's body suitable for detecting characteristics, symptoms or attributes of the condition or disorder being treated, for example, such as electrical brain activity, cerebral blood flow, and/or vital signs or other chemical and electrical activity of the body. Sensors suitable for use in a system according to the present invention include, for example, those disclosed in U.S. Patent No. 5,711,316, which is incorporated by reference herein. In cases where the attribute of the symptom is the electrical activity of the brain, stimulating electrodes may be intermittently used to record electrical activity. Alternatively, one or more electrodes implanted or positioned within the brain may serve as a sensor or a recording electrode. When necessary, these sensing or recording electrodes may deliver stimulation therapy to the target region. The output of an external feedback sensor may communicate with a pulse generator through a telemetry down-link. Any sensing functions in accordance with the present invention can be performed locally, distally, or remotely from the target site. The present invention also contemplates use of electrode assembly 10 integrated with imaging methods known in the art such as X-rays, computer tomography, magnetic resonance imaging, and functional magnetic resonance imaging.

0023Electrode assembly 10 may also be implemented within a drug delivery system to provide chemical stimulation utilizing a drug, pharmaceutical, or therapeutic agent. In this embodiment, the signal generator is replaced with or includes a pump and electrical contacts 10 are replaced with a drug ports. The pump may be implanted below the skin of a patient and may have a port into which a hypodermic needle can be inserted through the skin to inject a quantity of a liquid, such as a drug, pharmaceutical, or therapeutic agent. The liquid agent is delivered from a pump through a catheter port into a catheter. Alternatively, the pump maybe located outside of the patient's body. The catheter is positioned to deliver the liquid agent to specific infusion sites in the brain or other target site. Alternatively, electrode assembly 10 may be combined with a drug delivery system to provide both chemical and electrical signals to target regions.

0024Referring to FIG. 4, in another embodiment, the present invention provides a catheter 80 having multiple lumens, wherein one of the multiple lumens houses electrode assembly 10. In a preferred embodiment, catheter 80 is a pulmonary artery catheter, such as a Swan-Ganz type pulmonary artery catheter, wherein the multiple lumens allow for the measurement of cardiac output, pulmonary pressure, atrial pressure, and for providing an electrical signal to a target site adjacent a lumen. Specifically, in an embodiment catheter 80 comprises a thermistor lumen 31 housing a thermistor 32 to measure cardiac output; a pulmonary artery distal lumen 41 housing a sensor 42 to measure pulmonary artery pressure or pulmonary capillary wedge pressure; a proximal right atrial lumen 51 housing a sensor 52 to measure right atrial or central venous pressure; a balloon lumen 71 housing a balloon 72 to isolating the right chamber of the heart from the left chamber; and an electrode lumen 61 housing electrode assembly 10.

0025In an exemplary method of using catheter 80 in a pulmonary artery, catheter 80 is delivered and implanted in a manner similar to the delivery and implantation process used in currently available pulmonary artery catheters. Referring to FIG. 5 and FIG. 6, after venous access, catheter 80 is passed through an introducer up to a 20cm mark. Then,, balloon 72 at the distal end of balloon lumen 71 is inflated and pressure and tracings are recorded. As soon as catheter 80 is advanced to the point where'the inflated balloon 72 occludes the pulmonary artery, a wedge pulmonary pressure can be obtained from the sensor of pulmonary artery distal lumen 41. This pressure indication provides the physician the necessary feedback that the distal end of catheter 80 is well positioned in the pulmonary artery. Once adequate positioning is achieved, the electrode assembly 10 is urged forward out from electrode lumen 61 to the walls of the pulmonary artery. X- ray and fluoroscopy can be used to aid in positioning catheter 80. Such a method could be used to apply an electrical signal to a target site adjacent a pulmonary nerve, such as cardiac nerves to modulate the activity thereof. Of course, such a method of delivering catheter 80 is only exemplary and catheter 80 is not limited by any particular method of delivery and implantation.

0026The foregoing description has been set forth merely to illustrate the invention and are not intended as being limiting. Each of the disclosed aspects and embodiments of the present invention may be considered individually or in combination with other aspects, embodiments, and variations of the invention. In addition, unless otherwise specified, none of the steps of the methods of the present invention are confined to any particular order of performance. Further, although electrode assembly 10 is occasionally described with respect to neuromodulation, electrode assembly 10 is not limited to this particular use. Modifications of the disclosed embodiments incorporating the spirit and substance of the invention may occur to persons skilled in the art and such modifications are within the scope of the present invention. For example, although catheter 80 is described as have a balloon lumen 71 with a balloon 72 at the distal end thereof, other embodiments can include catheter 80 having multiple lumens without a balloon. Furthermore, all references cited herein are incorporated by reference in their entirety.