AU2012232971B2 - System and method for delivering energy to tissue - Google Patents

Abstract

SYSTEM AND METHOD FOR DELIVERING ENERGY TO TISSUE A system (10) for ablating tissue comprises an elongate shaft having a proximal portion, a distal portion and a longitudinal axis, and an ultrasound transducer (12) coupled to the distal portion of the elongate shaft, wherein the ultrasound transducer is adapted to deliver a beam (20) of ultrasound energy and the beam of energy ablates target tissue without contact between the ultrasound transducer (12) and the target tissue. The beam (20) of ultrasound energy is emitted in a direction relatively transverse to the longitudinal axis of the elongate shaft and forms a continuous lesion in the target tissue.

Description

Editorial Note 2012232971 Please note that the inventor "James W. Areson" on the cover sheet should be "James W. Arenson".

S&F Ref: 982221D1 AUSTRALIA PATENTS ACT 1990 COMPLETE SPECIFICATION FOR A STANDARD PATENT Name and Address Vytronus, Inc., of 658 N. Pastoria Avenue, Sunnyvale, of Applicant : California, 94086, United States of America Actual Inventor(s): David A. Gallup James W. Areson Hira V. Thapliyal Address for Service: Spruson & Ferguson St Martins Tower Level 35 31 Market Street Sydney NSW 2000 (CCN 3710000177) Invention Title: System and method for delivering energy to tissue The following statement is a full description of this invention, including the best method of performing it known to me/us: 5845c(6744617_1) 1 SYSTEM AND METHOD FOR DELIVERING ENERGY TO TISSUE BACKGROUND OF THE INVENTION 100011 Field of the Invention. The present invention relates generally to medical devices, systems and methods, and more specifically to improved devices, systems and methods for creating an ablation zone in tissue. The device may be used to treat atrial fibrillation. [00021 The condition of atrial fibrillation (AF) is characterized by the abnormal (usually very rapid) beating of the left atrium of the heart which is out of synch with the normal synchronous movement ("normal sinus rhythm") of the heart muscle. In normal sinus rhythm, the electrical impulses originate in the sino-atrial node ("SA node") which resides in the right atrium. The abnormal beating of the atrial heart muscle is known as fibrillation and is caused by electrical impulses originating instead in the pulmonary veins ("PV") [Haissaguerre, M. et al., Spontaneous Initiation of Atrial Fibrillation by Ectopic Beats Originating in the Pulmonary Veins, New England J Med., Vol. 339:659-666]. [00031 There are pharmacological treatments for this condition with varying degrees of success. In addition, there are surgical interventions aimed at removing the aberrant electrical pathways from the PV to the left atrium ("LA") such as the Cox-Maze III Procedure [J. L. Cox et al., The development of the Maze procedure for the treatment of atrial fibrillation, Seminars in Thoracic & Cardiovascular Surgery, 2000; 12: 2-14; J. L. Cox et al., Electrophysiologic basis, surgical development, and clinical results of the maze procedure for atrial flutter and atrial fibrillation, Advances in Cardiac Surgery, 1995; 6: 1-67; and J. L. Cox et al., Modification of the maze procedure for atrial flutter and atrial fibrillation. II, Surgical technique of the maze III procedure, Journal of Thoracic & Cardiovascular Surgery, 1995; 2110:485-95]. This procedure is shown to be 99% effective [J. L. Cox, N. Ad, T. Palazzo, et al. Current status of the Maze procedure for the treatment of atrial fibrillation, Seminars in Thoracic & Cardiovascular Surgery, 2000; 12: 15-19] but requires special surgical skills and is time consuming. [0004] There has been considerable effort to copy the Cox-Maze procedure for a less invasive percutaneous catheter-based approach. Less invasive treatments have been developed which involve use of some form of energy to ablate (or kill) the tissue surrounding the aberrant focal point where the abnormal signals originate in the PV. The most common 2 methodology is the use of radio-frequency ("RF") electrical energy to heat the muscle tissue and thereby ablate it. The aberrant electrical impulses are then prevented from traveling from the PV to the atrium (achieving conduction block within the heart tissue) and thus avoiding the fibrillation of the atrial muscle. Other energy sources, such as microwave, laser, and ultrasound have been utilized to achieve the conduction block. In addition, techniques such as cryoablation, administration of ethanol, and the like have also been used. [00051 There has been considerable effort in developing catheter based systems for the treatment of AF using radiofrequency (RF) energy. One such method is described in US Patent 6,064,902 to Haissaguerre et al. In this approach, a catheter is made of distal and proximal electrodes at the tip. The catheter can be bent in a J shape and positioned inside a pulmonary vein. The tissue of the inner wall of the pulmonary vein (PV) is ablated in an attempt to kill the source of the aberrant heart activity. Other RF based catheters are described in US Patents 6,814,733 to Schwartz et al., 6,996,908 to Maguire et al., 6,955,173 to Lesh, and 6,949,097 to Stewart et al. [00061 Another source used in ablation is microwave energy. One such device is described by Dr. Mark Levinson [(Endocardial Microwave Ablation: A New Surgical Approach for Atrial Fibrillation; The Heart Surgery Forum, 2006] and Maessen et al. [Beating heart surgical treatment of atrial fibrillation with microwave ablation. Ann Thorac Surg 74: 1160-8, 2002]. This intraoperative device consists of a probe with a malleable antenna which has the ability to ablate the atrial tissue. Other microwave based catheters are described in US Patents 4,641,649 to Walinsky; 5,246,438 to Langberg; 5,405,346 to Grundy et al.; and 5,314,466 to Stem et al. [00071 Another catheter based method utilizes the cryogenic technique where the tissue of the atrium is frozen below a temperature of -60 degrees C. This results in killing of the tissue in the vicinity of the PV thereby eliminating the pathway for the aberrant signals causing the AF [A. M. Gillinov, E. H. Blackstone and P. M. McCarthy, Atrial fibrillation: current surgical options and their assessment, Annals of Thoracic Surgery 2002; 74:2210-7). Cryo based techniques have been a part of the partial Maze procedures [Sueda T., Nagata H., Orihashi K. et al., Efficacy of a simple left atrial procedure for chronic atrial fibrillation in mitral valve operations, Ann Thorac Surg 1997; 63:1070-1075; and Sueda T., Nagata H., Shikata H. et al.; Simple left atrial procedure for chronic atrial fibrillation associated with mitral valve disease, Ann Thorac Surg 1996; 62: 1796-1800]. More recently, Dr. Cox and his group [Nathan H., Eliakim M., The junction between the left atrium and the pulmonary veins, An anatomic study of human hearts, Circulation 1966; 34:412-422, and Cox J.L., Schuessler 3 R.B., Boineau J.P., The development of the Maze procedure for the treatment of atrial fibrillation, Semin Thorac Cardiovasc Surg 2000; 12:2-14] have used cryoprobes (cryo Maze) to duplicate the essentials of the Cox-Maze III procedure. Other cryo-based devices are described in US Patents 6,929,639 and 6,666,858 to Lafintaine and 6,161,543 to Cox et al. [00081 More recent approaches for the AF treatment involve the use of ultrasound energy. The target tissue of the region surrounding the pulmonary vein is heated with ultrasound energy emitted by one or more ultrasound transducers. One such approach is described by Lesh et al. in US Patent 6,502,576. Here the catheter distal tip portion is equipped with a balloon which contains an ultrasound element. The balloon serves as an anchoring means to secure the tip of the catheter in the pulmonary vein. The balloon portion of the catheter is positioned in the selected pulmonary vein and the balloon is inflated with a fluid which is transparent to ultrasound energy. The transducer emits the ultrasound energy which travels to the target tissue in or near the pulmonary vein and ablates it. The intended therapy is to destroy the electrical conduction path around a pulmonary vein and thereby restore the normal sinus rhythm. The therapy involves the creation of a multiplicity of lesions around individual pulmonary veins as required. The inventors describe various configurations for the energy emitter and the anchoring mechanisms. 100091 Yet another catheter device using ultrasound energy is described by Gentry et al. [Integrated Catheter for 3-D Intracardiac Echocardiography and Ultrasound Ablation, IEEE Transactions on Ultrasonics, Ferroelectrics, and Frequency Control, Vol. 51, No. 7, pp 799 807]. Here the catheter tip is made of an array of ultrasound elements in a grid pattern for the purpose of creating a three dimensional image of the target tissue. An ablating ultrasound transducer is provided which is in the shape of a ring which encircles the imaging grid. The ablating transducer emits a ring of ultrasound energy at 10 MHz frequency. In a separate publication [Medical Device Link, Medical Device and Diagnostic Industry, February 2006], in the description of the device, the authors assert that the pulmonary veins can be imaged. 100101 While these devices and methods are promising, improved devices and methods for creating a heated zone of tissue, such as an ablation zone are needed. Furthermore, it would also be desirable if such devices could create single or multiple ablation zones to block abnormal electrical activity in the heart in order to lessen or prevent atrial fibrillation. It would also be desirable if such devices could be used in the presence of blood or other body tissues without coagulating or clogging up the ultrasound transducer. Such devices and methods should be easy to use, minimally invasive, cost effective and simple to manufacture.

4 [0011] Description of Background Art. Other devices based on ultrasound energy to create circumferential lesions are described in US Patent Nos. 6,997,925; 6,966,908; 6,964,660; 6,954,977; 6,953,460; 6,652,515; 6,547,788; and 6,514,249 to Maguire et al.; 6,955,173; 6,052,576; 6,305,378; 6,164,283; and 6,012,457 to Lesh; 6,872,205; 6,416,511; 6,254,599; 6,245,064; and 6,024,740; to Lesh et al.; 6,383,151; 6,117,101; and WO 99/02096 to Diederich et al.; 6,635,054 to Fjield et al.; 6,780,183 to Jimenez et al.; 6,605,084 to Acker et al.; 5,295,484 to Marcus et al.; and WO 2005/1 17734 to Wong et al. OBJECT OF THE INVENTION [0012] It is the object of the present invention to substantially overcome or at least ameliorate one or more of the above disadvantages. BRIEF SUMMARY OF THE INVENTION [0013] The present invention relates generally to medical devices and methods, and more specifically to medical devices and methods used to deliver energy to tissue as a treatment for atrial fibrillation and other medical conditions. [0014] There is disclosed herein a system for ablating tissue, said system comprising: an elongate shaft having a proximal portion, a distal portion, and a longitudinal axis; an ultrasound transducer disposed in a housing, the housing coupled to the distal portion of the elongate shaft; and a fluid flow controller for increasing or decreasing a fluid flow of a fluid flowing past the ultrasound transducer to prevent blood from coagulating thereon; wherein the ultrasound transducer is adapted to deliver a beam of collimated ultrasound energy from an inner surface of the tissue outward toward an outer surface of the tissue, and wherein the collimated beam of ultrasound energy ablates target tissue without contact between the ultrasound transducer and the target tissue, and wherein the collimated beam of ultrasound energy is emitted in a direction relatively transverse to the longitudinal axis of the elongate shaft, and wherein the collimated beam of ultrasound energy forms a continuous lesion in the target tissue.

5 [0015] There is further disclosed herein a method for ablating tissue, said method comprising: providing an ultrasound transducer disposed in a housing, the housing coupled to a distal portion of an elongate shaft; positioning the ultrasound transducer adjacent target tissue; flowing a fluid past the ultrasound transducer to prevent blood from coagulating thereon; increasing or decreasing a fluid flow of the fluid with a fluid flow controller; delivering a collimated beam of ultrasound energy from the ultrasound transducer to the target tissue, wherein the beam of ultrasound energy is emitted in a direction relatively transverse to a longitudinal axis of the elongate shaft; and ablating the target tissue with the beam of ultrasound energy from an inner surface of the tissue toward and outer surface of the tissue, and without contact between the ultrasound transducer and the target tissue, and wherein the beam of ultrasound energy forms a continuous lesion in the target tissue. [0016] This and other embodiments are described in further detail in the following non limiting description related to the appended drawing figures. BRIEF DESCRIPTION OF THE DRAWINGS [0017] FIGURES 1 and 2 are drawings of the system of the preferred embodiments of the invention; [0018] FIGURES 3A-3B illustrate the reflecting surface of the system and energy beam of the preferred embodiments of the invention; and [0019] FIGURE 4-5 are drawings of the energy beam and the zone of ablation of the preferred embodiment of the invention. DETAILED DESCRIPTION OF THE INVENTION [0020] The following description of preferred embodiments of the invention is not intended to limit the invention to these embodiments, but rather to enable any person skilled in the art to make and use this invention.

5a [0021] As shown in FIGURE 1, the energy delivery system 10 of the preferred embodiments includes an energy source 12 that functions to provide a source of ablation energy; a reflecting surface 100 that functions to redirect the ablation energy from the energy source 12; a sensor; and a processor (not shown), coupled to the sensor and to the energy source 12, which may controls the energy source 12 based on the information from the sensor. The energy delivery system 10 is preferably designed for delivering energy to tissue, more specifically, for delivering ablation energy to tissue, such as heart tissue, to create a 6 conduction block - isolation and/or block of conduction pathways of abnormal electrical activity, which typically originate from the pulmonary veins in the left atrium - for treatment of atrial fibrillation in a patient. The system 10, however, may be alternatively used with any suitable tissue in any suitable environment and for any suitable reason. [0032] The Energy Source. As shown in FIGURE 1, the energy source 12 of the preferred embodiments functions to provide a source of ablation energy. The ablation energy is preferably in the form of an energy beam 20 emitted from the energy source 12. The energy source 12 is preferably an ultrasound transducer that emits an ultrasound beam, but may alternatvely-be-any-suitable-energy source that functions to provide a source of ablation energy. Some suitable sources of ablation energy may include radio frequency (RF) energy, microwaves, photonic energy, and thermal energy. The therapy could alternatively be achieved using cooled fluids (e.g., cryogenic fluid). The energy delivery system 10 preferably includes a single energy source 12, but may alternatively include any suitable number of energy sources 12. For example, the system 10 may include multiple energy sources configured in a ring, such that in combination they emit an annular shaped energy beam 20. [00331 The energy source 12 is preferably an ultrasound transducer that is preferably made of a piezoelectric material such as PZT (lead zirconate titanate) or PVDF (polyvinylidine difluoride), or any other suitable ultrasound beam emitting material. The transducer may further include coating layers such as a thin layer of a metal. Some suitable transducer coating metals may include gold, stainless steel, nickel-cadmium, silver, plastic, metal-filled graphite, a metal alloy, and any other suitable material that functions to increase the efficiency of coupling of the energy beam 20 into the surrounding fluid 28 or performs any other suitable functions. The transducer is preferably a cylindrical transducer, as shown in FIGURES 3A and 3B, such that it preferably emits energy beam 20 from the outer face of the cylinder (e.g. radially out from the face of the energy source). The energy beam 20 is preferably emitted radially 360 degrees around the energy source 12, but may alternatively be emitted from any suitable portions) of the energy source. The transducer may alternatively be a generally flat transducer, such as a disc, as shown in FIGURES 1 and 2. The disc transducer preferably emits energy beam 20 from at least one of the faces of the disc. The faces of the disc that emit the energy beam 20 are preferably flat, but may alternatively be either concave or convex to achieve an effect of a lens. The disc transducer preferably has a circular geometry, but may alternatively be elliptical, polygonal, doughnut shaped, or any other suitable shape.

7 [00341 As shown in FIGURE 1, the energy source 12 of the preferred embodiments is preferably coupled to at least one electrical attachment 14. The electrical attachment 14 of the preferred embodiments functions to energize the energy source 12 such that it emits an energy beam 20. The energy delivery system 10 preferably includes two electrical attachments 14 and 14', but may alternatively include any suitable number of electrical attachments to energize the energy source 12. The energy delivery system 10 of the preferred embodiments also includes an electrical generator (not shown) that functions to provide power to the energy source 12 via the electrical attachment(s) 14. When energized by the generator the energy source 12 emits an energy beam 20. The generator provides the appropriate frequency and voltage to the energy source 12 to create the desired energy beam 20. In the case of an ultrasound energy source 12, the ultrasound frequency is preferably in the range of I to 25 MHz and more preferably in the range of 5 to 20 MHz. The energy of the energy beam 20 is determined by the excitation voltage applied to the energy source 12. The voltage is preferably in the range of 5 to 300 volts peak-to-peak. In addition, a variable duty cycle is preferably used to control the average power delivered to the energy source 12. The duty cycle preferably ranges from 0% to 100%, with a repetition frequency of approximately 40 kHz, which is preferably faster than the time constant of thermal conduction in the tissue. [00351 When energized with an electrical pulse or pulse train by the electrical attachment 14 and/or 14', the energy source 12 emits an energy beam 20 (such as a sound wave). The properties of the energy beam 20 are determined by the characteristics of the energy source 12, the matching layer, the backing (described below), and the electrical pulse from electrical attachment 14. These elements determine the frequency, bandwidth, and amplitude of the energy beam 20 (such as a sound wave) propagated into the tissue. As shown in FIGURE 4, the energy source 12 emits energy beam 20 such that it interacts with tissue 276 and forms a lesion (zone of ablation 278). The energy beam 20 is preferably an ultrasound beam. The tissue 276 is preferably presented to the energy beam 20 within the collimated length L. The front surface 280 of the tissue 276 is at a distance d (282) away from the face of a housing 16. As the energy beam 20 travels through the tissue 276, its energy is absorbed by the tissue 276 and converted to thermal energy. This thermal energy heats the tissue to temperatures higher than the surrounding tissue resulting in a heated zone 278. In the zone 278 where the tissue is heated, the tissue cells are preferably rendered dead due to heat. The temperatures of the tissue are preferably above the temperature where cell death occurs in the heated zone 278 and therefore, the tissue is said to be ablated. Hence, the zone 278 is preferably referenced as the ablation zone or lesion.

8 [00361 The shape of the lesion or ablation zone 278 formed by the energy beam 20 depends on the characteristics of suitable combination factors such as the energy beam 20, the energy source 12 (including the material, the geometry, the portions of the energy source 12 that are energized and/or not energized, etc.), the matching layer, the backing, the electrical pulse from electrical attachment 14 (including the frequency, the voltage, the duty cycle, the length of the pulse, etc.), and the characteristics of target tissue that the beam 20 contacts and the length of contact or dwell time. These characteristics can be changed based on the information detected by the sensor (as described below), thereby changing the physical characteristics of the lesion. 100371 The housing 16 also functions to provide a barrier between the face of the energy source 12 and blood or tissue. When fluid flow is incorporated, the fluid may flow past the energy source thereby preventing blood from coagulating thereon. In preferred embodiments, the coolant flows past the energy source at approximately 1 ml/minute, but may be increased or decreased as desired. Additionally, since the energy source is disposed in the housing, the energy source will not directly contact tissue, thereby also preventing coagulation on the energy source. [00381 Additional details on the energy source, energy source configurations, the housing and adjacent components are disclosed in U.S. Patent Application Nos. 12/480,256 (Attorney Docket No. 027680-00031OUS) and 12/482,640 (Attorney Docket No. 027680-000510US), the entire contents of which are incorporated herein by reference. 100391 The Reflecting Surface. As shown in FIGURE 1, the reflector 100 of the preferred embodiments functions to redirect the energy beam 20 from the energy source 12. The reflecting surface 100 preferably redirects the energy beam 20 from the energy source 12 out of housing 16 and preferably towards the target tissue. The reflecting surface 100 preferably redirects the energy beam 20 such that it is a collimated beam exiting the housing 16 (as shown in FIGURE 2 and 3), the reflecting surface 22 may alternatively redirect the energy beam 20 such that it is a focused beam that preferably converges towards a substantially single focal point or towards focal point ring. The reflecting surface is preferably one of several variations. In a first variation, as shown in FIGURE 1, the reflecting surface 100 is an angled reflector device. The reflector device is preferably a cylindrical reflector with a face of the reflector at an angle to the longitudinal axis of the housing 16. The energy source 12 is preferably positioned towards the distal end of the housing 16 with the front face pointing towards the reflector device, which is preferably positioned along the same axis (the longitudinal axis of the housing 16) as the energy source 12. The energy beam 20 from the 9 energy source 12 is preferably redirected from the reflecting surface such that it exits the housing 16 through a side portion of the housing. The reflector device is preferably made from a material that reflects the energy beam 20, such as metal, but may alternatively be a gas filled reflector device such as a gas filled balloon. The angled face of the reflector is preferably flat, but may alternatively be a non-planar face, such as a curved, convex or concave surface. The angle of the reflector preferably ranges between substantially 0 degrees, more preferably substantially 30-60 degrees, and most preferably substantially 45 degrees. The reflector device is preferably set at a fixed angle with respect to the energy source 12, but may alternatively be movable, such as rotated or pivoted, to alter the angle that the energy beam 20 will exit the housing 16. Referring to FIGURE 1, the reflector device is preferably secured to the housing 16 by means of a distal adhesive band 1418, but may alternatively be coupled to the housing 16 with any other suitable chemical and/or mechanical connection such as adhesive, welding, pins and/or screws. The adhesive band 1418 preferably includes a passageway 1445 for the flow of a cooling fluid (as described below). 100401 In the first variation of the reflecting surface 100, the energy beam 20 exiting from the housing 16 is preferably directed along an ablation path such that it propagates into tissue. As the energy beam 20 propagates into the tissue along the ablation path, it preferably provides a partial or complete zone of ablation along the ablation path. The zone of ablation along the ablation path preferably has any suitable geometry to provide therapy, such as providing a conduction block for treatment of atrial fibrillation in a patient. The zone of ablation along the ablation path may alternatively provide any other suitable therapy for a patient. A linear ablation path is preferably created by moving the system 10, and the energy source 12 within it, in an X, Y, and/or Z direction. A generally circular or elliptical ablation path is preferably created by rotating the energy source 12 about an axis. In a first version, the reflecting surface 100 is preferably rotated within the housing 16 and about the longitudinal axis of the housing 16, such that as the energy source 12 is energized and emitting the energy beam 20, the beam will be reflected out of the housing in 360 degrees. The energy beam 20 that is redirected by the reflecting surface 100 preferably exits a side portion of the housing though a window located around the circumference of the distal tip assembly 16. The window is preferably made of a material that is transparent to ultrasound waves such as a poly 4-methyl, 1 -pentene (PMP) material or may alternatively be an open window. In a second version, the entire system 10 will rotate, rotating the energy beam 20 that exits from at least one single portion of the housing 16. The system 10 is preferably 10 rotated about the longitudinal axis of the housing 16, but may alternatively be rotated about an axis off set from the longitudinal axis of the housing 16. In this version, the energy beam 20 preferably sweeps a generally circular path. [0041] In a second variation, as shown in FIGURE 2, the reflecting surface 100 is also an angled reflector device. The reflector device is preferably a substantially flat reflecting device, with an inside face of the reflector at an angle to the front face of the energy source 12. The energy source 12 is preferably positioned adjacent to a side wall of the housing 16 with the front face the energy source 12 pointing towards the reflector device. The energy beam 20 from the energy source 12 is preferably redirected from the reflecting surface such that it exits the housing 16 through an end portion of the housing. The energy beam 20 that is redirected by the reflecting surface 100 preferably exits the end portion of the housing though a window. The window is preferably an open window, but may alternatively be made of a material that is transparent to ultrasound waves such as a poly 4-methyl, I -pentene (PMP) material. The reflector device is preferably made from a material that reflects the energy beam 20, such as metal, but may alternatively be a gas filled reflector device such as a gas filled balloon. The angled face of the reflector is preferably flat, but may alternatively be a nonplanar face, such as a curved, convex or concave surface. The angle of the reflector preferably ranges between substantially 0-90 degrees, more preferably substantially 30-60 degrees, and most preferably substantially 45 degrees. The reflector device is preferably set at a fixed angle with respect to the energy source 12, but may alternatively be movable, such as rotated or pivoted, to alter the angle that the energy beam 20 will exit the housing 16. The reflecting surface 22 preferably includes a passageway 1445 for the flow 28 of a cooling fluid (as described below). [0042] In the second variation of the reflecting surface 100, the energy beam 20 exiting from the housing 16 is preferably directed along an ablation path such that it propagates into tissue. As the energy beam 20 propagates into the tissue along the ablation path, it preferably provides a partial or complete zone of ablation along the ablation path. A linear ablation path is preferably created by moving the system 10, and the energy source 12 within it, in an X, Y, and/or Z direction. Alternatively, a generally circular or elliptical ablation path is preferably created by rotating the housing 16 about an axis. In a first version, the housing 16 is preferably rotated about its longitudinal axis. Because the energy beam 20 is redirected by the reflecting surface 100, as shown in FIGURE 2, the energy beam 20 exits the housing at a distance from the longitudinal axis of the housing. Therefore, as the housing 16 is moved in a 11 circular or elliptical path, the energy beam 20 will contact the tissue, creating a corresponding generally circular or elliptical ablation path. 100431 In a third variation, as shown in FIGURES 3A and 3B, the reflecting surface 100 is also an angled, bowl-shaped reflector device centered around the longitudinal axis of the housing 16. The inside surface of the reflector device is preferably a substantially linear surface (in cross section, as shown in FIGURE 3B) at an angle to the front face of the energy source 12. The angled face of the reflector is preferably flat, but may alternatively be a non planar face, such as a curved, convex or concave surface, or combinations thereof. The energy source 12 is preferably a cylindrical energy source 12, positioned along the longitudinal axis of the housing 16. The energy beam 20 from the energy source 12 preferably exits the energy source radially and is preferably redirected from the reflecting surface such that it exits the housing 16 as a ring shaped energy beam (as shown in FIGURE 3A) through an end portion of the housing. The energy beam 20 that is redirected by the reflecting surface 100 preferably exits the end portion of the housing though a window. The window is preferably an open window, but may alternatively be made of a material that is transparent to ultrasound waves such as a poly 4-methyl, I -pentene (PMP) material. The reflector device is preferably made from a material that reflects the energy beam 20, such as metal, but may alternatively be a gas filled reflector device such as a gas filled balloon. The angle of the reflector preferably ranges between substantially 0-90 degrees, more preferably substantially 30-60 degrees, and most preferably substantially 45 degrees. The reflector device is preferably set at a fixed angle with respect to the energy source 12, but may alternatively be movable, such as rotated or pivoted, to alter the angle that the energy beam 20 will exit the housing 16. 100441 In the third variation of the reflector 100, the energy beam 20 exiting from the housing 16 is preferably ring-shaped, as shown in FIGURE 3A, and therefore preferably creates a ring shaped ablation path when it interacts with tissue and preferably provides a partial or complete zone of ablation along the ablation path. A linear ablation path is alternatively created by the energy source 12 emitting energy beam 20 from only a partial radial portion of the energy source and/or by moving the system 10, and the energy source 12 within it, in an X, Y, and/or Z direction. Alternatively, the energy source of the third variation reflecting surface 100 may be a flat energy source (rather than a cylindrical one) with the front face towards a portion of the reflecting surface. To create an ablation path, the energy source 12 is preferably rotated about the longitudinal axis of the housing such that the energy 12 beam 20 will be redirected by various portions of the reflecting surface, creating a circular ablation path. 100451 The Sensor. As shown in FIGURE 5, the energy delivery system 10 of the preferred embodiments also includes a sensor that functions to detect the gap (e.g., the distance of the tissue surface from the energy source 12), the thickness of the tissue targeted for ablation, and the characteristics of the ablated tissue. The sensor is preferably an ultrasound transducer, but may alternatively be any suitable sensor, such as a strain gage, feeler gage, or IR sensor, to detect information with respect to the gap, the thickness of the tissue targeted for ablation, the characteristics of the ablated tissue, the location of elements of the system 10, and/or any other suitable parameter or characteristic. [00461 The sensor is preferably the same transducer as the transducer of the energy source 12 operating in a different mode (such as A-mode, defined below), but may alternatively be a separate ultrasound transducer or an additional sensor 40' as shown in FIGURE 3A coupled to a top portion of the cylindrical energy source 12. The system 10 may include multiple sensors such as a first sensor to detect information with respect to the target tissue, and a second sensor to detect information with respect to the location of the elements of the system 10. By detecting information on the gap, the thickness of the tissue targeted for ablation, the characteristics of the ablated tissue, and/or the locations of the elements of the system 10, the sensor preferably functions to guide the therapy provided by the ablation of the tissue. [00471 In the variations of the system 10 wherein the sensor is the same transducer as the transducer of the energy source 12 operating in a different mode (such as A-mode), the sensor preferably utilizes a pulse of ultrasound of short duration, which is generally not sufficient for heating of the tissue. This is a simple ultrasound imaging technique, referred to in the art as A Mode, or Amplitude Mode imaging. As shown in FIGURE 5, sensor 40 preferably sends a pulse 290 of ultrasound towards the tissue 276. A portion of the beam is reflected and backscattered as 292 from the front surface 280 of the tissue 276. This reflected beam 292 is detected by the sensor 40 a short time later and converted to an electrical signal, which is sent to the electrical receiver (not shown). The reflected beam 292 is delayed by the amount of time it takes for the sound to travel from the sensor 40 to the front boundary 280 of the tissue 276 and back to the sensor 40. This travel time represents a delay in receiving the electrical signal from the sensor 40. Based on the speed of sound in the intervening media (fluid 286 and blood 284), the gap distance d (282) is determined. As the sound beam travels further into the tissue 276, a portion 293 of it is scattered from the lesion 278 being formed and travels towards the sensor 40. Again, the sensor 40 converts this sound energy into electrical 13 signals and a processor (described below) converts this information into characteristics of the lesion formation such as thickness, etc. As the sound beam travels still further into the tissue 276, a portion 294 of it is reflected from the back surface 298 and travels towards the transducer. Again, the sensor 40 converts this sound energy into electrical signals and the processor converts this information into the thickness t (300) of the tissue 276 at the point of the incidence of the ultrasound pulse 290. As the catheter housing 16 is traversed in a manner 301 across the tissue 276, the sensor 40 detects the gap distance d (282), lesion characteristics, and the tissue thickness t (300). The sensor preferably detects these parameters continuously, but may alternatively detect them periodically or in any other suitable fashion. This information is used in delivering continuous ablation of the tissue 276 during therapy as discussed below. 100481 The Processor. The energy delivery system 10 of the preferred embodiments also includes a processor, coupled to the sensor 40 and to the electrical attachment 14, that controls the electrical pulse delivered to the electrical attachment 14 and may modify the electrical pulse delivered based on the information from the sensor 40. The processor is preferably a conventional processor or logic machine that can execute computer programs including a microprocessor or integrated circuit, but may alternatively be any suitable device to perform the desired functions. [00491 The processor preferably receives information from the sensor such as information related to the gap distance, the thickness of the tissue targeted for ablation, the characteristics of the ablated tissue, and any other suitable parameter or characteristic. Based on this information, the processor converts this information into a gap distance, a thickness of the tissue targeted for ablation, a characteristic of the ablated tissue, and any other suitable parameter or characteristic and/or controls the energy beam 20 emitted from the energy source 12 by modifying the electrical pulse sent to the energy source 12 via the electrical attachment 14 such as the frequency, the voltage, the duty cycle, the length of the pulse, and/or any other suitable parameter. The processor preferably also controls the energy beam 20 by controlling which portions of the energy source 12 are energized and/or at which frequency, voltage, duty cycle, etc. different portions of the energy source 12 are energized. Additionally, the processor may further be coupled to a fluid flow controller. The processor preferably controls the fluid flow controller to increase or decrease fluid flow based on the sensor detecting characteristics of the ablated tissue, of the unablated or target tissue, and/ or any other suitable condition.

14 [0050] By controlling the energy beam 20 (and/or the cooling of the targeted tissue), the shape of the ablation zone 278 is controlled. For example, the depth 288 of the ablation zone is preferably controlled such that a transmural (through the thickness of the tissue) lesion is achieved. Additionally, the processor preferably functions to minimize the possibility of creating a lesion beyond the targeted tissue, for example, beyond the outer atrial wall. If the sensor detects the lesion extending beyond the outer wall of the atrium or that the depth of the lesion has reached or exceeded a preset depth, the processor preferably turns off the generator and/or ceases to send electrical pulses to the electrical attachment(s) 14. Additionally, if the sensor detects, for example, that the system 10 is not centered with respect to the pulmonary vein PV by detecting the distance of the target tissue with respect to the energy source and/or intended ablation path, the processor may either turn off the generator and/or cease to send electrical pulses to the electrical attachment(s) 14, may alter the pulses sent to the electrical attachment, and/or may alter the operator or motor drive unit to reposition the system with respect to the target tissue. 100511 Additional Elements. As shown in FIGURE 1, the energy delivery system 10 of the preferred embodiments may also include an elongate member 18, coupled to the energy source 12. The elongate member 18 is preferably a catheter made of a flexible multi-lumen tube, but may alternatively be a cannula, tube or any other suitable elongate structure having one or more lumens. The elongate member 18 of the preferred embodiments functions to accommodate pull wires, fluids, gases, energy delivery structures, electrical connections, therapy catheters, navigation catheters, pacing catheters, and/or any other suitable device or element. As shown in FIGURE 1, the elongate member 18 preferably includes a housing 16 positioned at a distal portion of the elongate member 18 that functions to enclose the energy source 12 and the reflection surface 100. The elongate member 18 further functions to move and position the energy source 12 and/or the housing 16 within a patient, such that the emitted energy beam 20 contacts the target tissue at an appropriate angle and the energy source 12 and/or the housing 16 is moved along an ablation path such that the energy source 12 provides a partial or complete zone of ablation along the ablation path. [00521 The energy delivery system 10 of the preferred embodiments may also include a lens or mirror, operably coupled to the energy source 12, that functions to provide additional flexibility in adjusting the beam pattern of the energy beam 20. The lens is preferably a standard acoustic lens, but may alternatively be any suitable lens to adjust the energy beam 20 in any suitable fashion. The lens may be used to focus or defocus the energy beam. For example, an acoustic lens could create a beam that is more uniformly collimated, such that 15 the minimum beam width D, approaches the diameter D of the energy source 12. This will provide a more uniform energy density in the ablation window, and therefore more uniform lesions as the tissue depth varies within the window. A lens could also be used to move the position of the minimum beam width D 1 , for those applications that may need either shallower or deeper lesion. This lens could be fabricated from plastic or other material with the appropriate acoustic properties, and bonded to the face of energy source 12. Alternatively, the energy source 12 itself may have a geometry such that it functions as a lens, or the matching layer or coating of the energy source 12 may function as a lens. 100531 Although omitted for conciseness, the preferred embodiments include every combination and permutation of the various energy sources 12, electrical attachments 14, energy beams 20, sensors 40, and processors. 100541 As a person skilled in the art will recognize from the previous detailed description and from the figures and claim, modifications and changes can be made to the preferred embodiments of the invention without departing from the scope of this invention defined in the following claims.

Claims (16)

1. A system for ablating tissue, said system comprising: an elongate shaft having a proximal portion, a distal portion, and a longitudinal axis; an ultrasound transducer disposed in a housing, the housing coupled to the distal portion of the elongate shaft; and a fluid flow controller for increasing or decreasing a fluid flow of a fluid flowing past the ultrasound transducer to prevent blood from coagulating thereon; wherein the ultrasound transducer is adapted to deliver a beam of collimated ultrasound energy from an inner surface of the tissue outward toward an outer surface of the tissue, and wherein the collimated beam of ultrasound energy ablates target tissue without contact between the ultrasound transducer and the target tissue, and wherein the collimated beam of ultrasound energy is emitted in a direction relatively transverse to the longitudinal axis of the elongate shaft, and wherein the collimated beam of ultrasound energy forms a continuous lesion in the target tissue.

2. The system of claim 1, further comprising a reflecting element operably coupled with the ultrasound transducer, the reflecting element redirecting the beam of ultrasound energy emitted from the ultrasound transducer to a desired direction or a pattern.

3. The system of claim 2, wherein the reflecting element is non-expandable.

4. The system of claim 2, wherein the reflecting element is movable relative to the ultrasound transducer so that the beam of ultrasound energy is emitted at varying angles or positions.

5. The system of claim 1, further comprising a sensor adjacent the ultrasound transducer, wherein the sensor senses distance between the ultrasound transducer and the target tissue, or the sensor senses properties of the target tissue.

6. The system of claim 5, wherein the properties of the target tissue comprise target tissue thickness or properties of the ablated target tissue. 17

7. The system of claim 5, wherein the ultrasound transducer and the sensor are the same ultrasound transducer.

8. The system of claim 1, wherein the lesion is a ring shape, elliptical shape, linear shape, curvilinear shape, or combinations thereof

9. A method for ablating tissue, said method comprising: providing an ultrasound transducer disposed in a housing, the housing coupled to a distal portion of an elongate shaft; positioning the ultrasound transducer adjacent target tissue; flowing a fluid past the ultrasound transducer to prevent blood from coagulating thereon; increasing or decreasing a fluid flow of the fluid with a fluid flow controller; delivering a collimated beam of ultrasound energy from the ultrasound transducer to the target tissue, wherein the beam of ultrasound energy is emitted in a direction relatively transverse to a longitudinal axis of the elongate shaft; and ablating the target tissue with the beam of ultrasound energy from an inner surface of the tissue toward and outer surface of the tissue, and without contact between the ultrasound transducer and the target tissue, and wherein the beam of ultrasound energy forms a continuous lesion in the target tissue.

10. The method of claim 9, wherein delivering the beam of ultrasound energy comprises reflecting the beam of ultrasound energy off of a reflecting element operably coupled with the ultrasound transducer thereby redirecting the beam of ultrasound energy to a desired direction or pattern.

11. The method of claim 10, wherein reflecting the beam of ultrasound energy comprises moving the reflecting element relative to the ultrasound transducer so that the beam of ultrasound energy is emitted at varying angles or positions.

12. The method of claim 9, further comprising sensing distance between the ultrasound transducer and the target tissue with a sensor, or sensing properties of the target tissue with the sensor.

13. The method of claim 12, wherein the ultrasound transducer and the sensor are the same ultrasound transducer. 18

14. The method of claim 9, wherein the lesion is a ring shape, elliptical shape, linear shape, curvilinear shape, or combinations thereof

15. A system, substantially as hereinbefore described with reference to the accompanying drawings.

16. A method, substantially as hereinbefore described with reference to the accompanying drawings. Vytronus, Inc. Patent Attorneys for the Applicant/Nominated Person SPRUSON & FERGUSON