WO1997040760A1

WO1997040760A1 - A system for simultaneous unipolar multi-electrode ablation

Info

Publication number: WO1997040760A1
Application number: PCT/AU1997/000258
Authority: WO
Inventors: Michael Daly; Pramesh Kovoor; Konstadinos Hatzianestis; David Ross
Original assignee: Cardiac Crc Nominees Pty. Ltd.
Priority date: 1996-04-30
Filing date: 1997-04-30
Publication date: 1997-11-06
Also published as: AUPN957296A0; US20010020166A1; US6346104B2

Abstract

A system (2, 4) method and splitter (6) for ablating tissue (15) using radiofrequency (RF) energy is disclosed. The system (2, 4) ablates tissue (15) using unipolar RF energy simultaneously delivered to multiple electrodes (22A-22D) in one or more probes (20). This is carried out by the multiple channel RF splitter (6) that can independently control the RF energy delivered through each channel (18) to a respective electrode (22A-22D) in a continuous manner. Each electrode (22A-22D) has a corresponding temperature sensor or transducer (36A-36D) that is processed independently so that the amount of RF energy delivered to each electrode (22A-22D) can be varied dependent on the temperature of the electrode (22A-22D) so that the lesion size produced by each electrode (22A-22D) can be accurately controlled. Preferably, each probe (20) has a needle-like structure with a number of electrodes (22A-22D) separated by insulative material and is adapted to puncture tissue. Each channel (18) of the splitter (6) has circuitry for interrupting current delivered to the respective channel if a predetermined temperature or current level is exceeded.

Description

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A System for Simultaneous Unipolar Multi-Electrode Ablation

Background

The present invention relates to a system, method and apparatus for ablating tissue under temperature control of each electrode to control lesion dimensions, and in particular for ablating myocardial tissue to treat Ventricular Tachycardia (VT) or atrial fibrillation/flutter (AF).

Ventricular tachycardia is a disease of the heart which causes the heart chambers to beat excessively fast and usually degenerates to ventricular fibrillation where the heart chambers do not effectively pump blood through the body's system and hence leads to death. Ventricular tachycardia is the most common cause of cardiac arrest and sudden death. Typical features of patients with VT are: (1) a history of myocardial infarction (heart attack), (2) significant left ventricular dysfunction (the main chamber effecting the pumping action), and (3) left ventricular aneurysm (dilation, thinning and stretching of the chamber). Detailed mapping studies of the electrical propagation within the myocardium during VT have shown that a re entrant pathway within and around the scarring (caused by infarction) is responsible for the arrhythmia. These studies have shown that the critical area of myocardium necessary to support reentry appears to be less than 2 to 4 cm^. Atrial fribillation (AF) and atrial flutter are diseases of the heart which can cause the heart to beat excessively fast and frequently in an erratic manner. This usually results in distress for patients. This may also be associated with clot formation in the atria, which may become dislodged and cause strokes. AF is usually due to abnormal electrical activation of the atria. Preliminary investigations have shown that linear lesions in the atria using radiofrequency ablation can cure these aπtiythmias .

A number of conventional techniques using radio frequency (RF) energy have been used to treat VT or AF. Endocardial radio frequency catheter ablation has been used in the treatment of hemodynamically stable monomorphic ventricular tachycardia secondary to coronary artery disease. The resulting lesions caused in RF ablation using catheters however have been insufficient in volume to destroy the area of tissue causing the arrhythmia.

Radiofrequency catheter ablation has been used for treatment of AF, but has been limited by the number of separate ablations required and the time required to perform the procedure.

In accordance with one conventional technique, RF energy is delivered from an RF source, incorporating phase shift networks to enable potential differences and hence current flow between multiple, separate electrode structures. Also, multiple RF power sources have been used connected to such electrodes. The independent phases of the power source lead to multiple current paths.

However, this conventional system lacks adequate temperature control because the multiphase RF ablation cannot function satisfactorily unless certain restrictions on the dimensions of the electrode are adhered to. The ablation temperature can only be maintained at an optimum predetermined level of approximately 80°C. This is a significant shortfall of the technique.

Summary

The present invention is directed to improving the efficacy of producing radio frequency lesions using multiple temperature controlled delivery by splitting high frequency current from a single generator into a number of electrodes simultaneously. Further, the system accurately measures the temperatures of these electrodes which are then used as the feedback in the system, allowing appropriate control strategies to be performed to regulate the current to each electrode.

In accordance with a first aspect of the invention, a system for ablating tissue comprises: a device for generating RF energy; a probe device comprising N separate electrodes, each having a corresponding device for sensing the temperature of the electrode; a splitter device for splitting the RF energy coupled to the generating device and the probe device, the splitter device having N separate channels each being coupled to a corresponding one of the N electrodes and temperature sensing device; and a device for controlling the splitter device, whereby the ablation of tissue at each electrode is independently controlled using closed loop feedback of the temperature of the electrode by independently regulating the amount of the RF energy delivered to each electrode.

Preferably, the system comprises a plurality of the probe devices and the splitter devices, and the controlling device separately controls each of the probe devices and the corresponding splitter device.

Preferably, the probe device has an elongated needle-like structure with one end adapted to puncture tissue and having sufficient rigidity to puncture the tissue, or a catheter which can be advanced into the heart. Each of the electrodes may consist of a circular metal surface separated one from another by insulation. Preferably, the RF energy has a single phase.

Preferably, the system further comprises a device for independently and continuously adjusting the RF energy delivered to each electrode in response to a control signal from the controlling device dependent on the temperature of the electrode. Preferably, the controlling device is programmable.

Optionally, the probe device is a catheter probe device. Preferably, each of the temperature sensing devices is a thermocouple. Preferably, the splitter device comprises one or more devices for independently interrupting current from the RF energy generating device to a respective electrode. In accordance with a second aspect of the invention, a medical apparatus for treatment by radiofrequency ablation of tissue comprises: an RF energy generator; one or more probes each comprising a plurality of separate electrodes and corresponding temperature sensors for sensing the temperature of the electrodes, each temperamre sensor connected to a respective one of the plurality of electrodes; a splitter for splitting the RF energy provided by the RF energy generator, the splitter having a plurality of separate channels, wherein each of the electrodes is coupled to a respective one of the plurality of channels; and a programmable controller coupled to the RF splitter for independently controlling the ablation of tissue at each electrode using closed loop feedback of the temperature of the electrode, whereby the amount of the RF energy delivered to each electrode is independently regulated by the programmable controller.

In accordance with a third aspect of the invention, a radio frequency energy splitter for use with one or more probes in a system for RF ablation of tissue is provided. Each probe comprises a plurality of separate electrodes and corresponding temperature sensors for sensing the temperature of the electrode. The splitter comprises: an input device for receiving RF energy from an RF energy generator; a plurality of channel modules for separately delivering RF energy from the input device to a respective electrode of the plurality of electrodes of the one or more probes, each channel module comprising: a device for variably adjusting an amount of the RF energy delivered to the respective electrode in response to a control signal, the variable adjusting device being coupled between the input device and the respective electrode; a device for interrupting the RF energy delivered to the respective electrode; an output device coupled to the respective temperamre sensor for providing a temperamre signal; a device for determining if the temperamre at the respective electrode exceeds a predetermined threshold and actuating the interrupting device if - -

the threshold is exceeded, whereby the RF energy is interrupted from delivery to the respective electrode; wherein each channel module is capable of receiving the respective control signal from and providing the respective temperamre signal to a programmable controller so that the amount of the RF energy delivered to each electrode can be independently regulated using closed loop feedback of the temperamre of each electrode.

Preferably, the variable adjusting device or circuit comprises a bridge rectifier including a fast-switching variable resistance for controlling operation of the bridge rectifier in response to the control signal.

Preferably, the RF energy interrupting device comprises a circuit for interrupting a current through the RF energy interrupting device and a circuit for limiting the current.

Preferably, the determining device compares the temperamre signal with the predetermined threshold.

In accordance with a fourth aspect of the invention, a method for ablating tissue comprises the steps of: generating RF energy; providing a probe device comprising N separate electrodes, each having a corresponding temperamre sensing device; measuring the temperamre of each electrode using the temperamre sensing device of the electrode; splitting the RF energy to the probe device into N separate channels each being coupled to a corresponding one of the N electrodes and temperamre sensing device; and controlling the splitting of the RF energy to the probe device, whereby the ablation of tissue at each electrode is independently controlled using closed loop feedback of the measured temperamre of the electrode by independently regulating the amount of the RF energy delivered to each electrode. Preferably, the method comprises the step of separately controlling the splitting of the RF energy to a plurality of the probe device.

Preferably, the probe device has an elongated needle-like structure with one end adapted to puncture tissue and having sufficient rigidity to puncture the tissue, wherein each of the electrodes consists of a metal substantially circular surface separated one from another by insulation.

Preferably, the RF energy has a single phase.

Preferably, the method fiirther comprises the step of independently and continuously adjusting the RF energy delivered to each electrode in response to a control signal from a programmable controlling device dependent on the temperamre of the electrode.

In accordance with a fifth aspect of the invention, a method for treatment by radiofrequency (RF) ablation of tissue comprises the steps of: generating RF energy; providing one or more probes each comprising a plurality of separate electrodes and corresponding temperamre sensors, each temperamre sensor connected to a respective one of the plurality of electrodes; measuring the temperamre of each electrode using the respective temperamre sensor; splitting the RF energy into a plurality of separate channels, wherein each of the electrodes is coupled to a respective one of the plurality of channels; and programmably controlling the splitting of the RF energy so as to independently control the ablation of tissue at each electrode using closed loop feedback of the measured temperamre of the electrode, whereby the amount of the RF energy delivered to each electrode is independently regulated.

Preferably, the method involves using at least two probes, and comprises the step of programmably controlling each of the probes separately.

In accordance with a sixth aspect of the invention, there is provided a method of splitting radio frequency energy delivered to one or more probes in a system for RF ablation of tissue. Each probe comprises a plurality of separate electrodes and corresponding temperamre sensors for sensing the temperamre of the electrode. The method comprises the steps of: receiving RF energy from an RF energy generator; providing a plurality of channel modules for separately delivering the RF energy to a respective electrode of the plurality of electrodes of the one or more probes, further comprising, for each channel module, the sub-steps of: variably adjusting an amount of the RF energy delivered to the respective electrode in response to a control signal; measuring the temperamre of the respective electrode using the corresponding temperamre sensor to provide a temperamre signal; determining if the temperamre at the respective electrode exceeds a predetermined threshold and interrupting delivery of the RF energy to the respective electrode if the threshold is exceeded; wherein each channel module is capable of receiving the respective control signal from and providing the respective temperamre signal to a programmable controller so that the amount of the RF energy delivered to each electrode can be independently regulated using closed loop feedback of the temperamre of each electrode. Preferably, the step of variably adjusting the RF energy comprises the step of changing the resistance of a fast-switching variable resistance incorporated in a bridge rectifier in response to the control signal.

Preferably, the step of interrupting the RF energy comprises the steps of interrupting a current to the respective electrode and limiting the current. Preferably, the step of determining comprises the step of comparing the temperamre signal with the predetermined threshold. Brief Description of the Drawings

Embodiments of the invention are described hereinafter with reference to the drawings, in which:

Fig. 1 is a block diagram of the RF ablation system according to one embodiment;

Fig. 2. is a detailed schematic of a single channel of the system of Fig. 1 ;

Fig. 3 is a detailed schematic of the system of Fig. 1 , wherein N = 4; and

Fig. 4 is a detailed schematic of a single channel of an RF ablation system according to another embodiment.

Detailed Description

First Embodiment The RF ablating system according to a first embodiment shown in Fig . 1 comprises a programmable controller 2, an N-channel RF splitter 6, an RF generator 8, a large conductive, dispersive plate 12, and an N-electrode probe 20. RF generators for RF ablation of tissue are well known in the art. It will be appreciated by a person skilled in the art that the present invention can be practiced with any of a number of RF generators without departing from the scope and spirit of the invention.

Preferably, the probe 20 has a needle-like structure wherein each of the electrodes 22 A to 22D has a mbular or ring shape. The electrodes 22 A to 22D are separated from each other by an intervening insulative portion. Such a probe structure is disclosed in International Publication No. WO 97/06727 published on 27 February 1997 (International Application No. PCT/AU96/00489 by the Applicant) and incoφorated herein by cross-reference. The structure of this probe 20 enables the electrodes 22A to 22D to be inserted into the myocardium for use in the present system. While this embodiment is described with reference to a single needle probe 20, the system may be practiced with a plurality of such needle probes 20 and one or more corresponding N-channel RF splitters 6 that are controlled by the programmable controller 2. It will be apparent to a person skilled in the art that the embodiment is not limited to the use of such needle-like probes but may be practiced with other types of ablating probes including catheters.

Further, while this embodiment is discussed with reference to ablation of reentrant pathways in relation to ventricular tachycardia, the system is not limited to this particular application, and instead can practiced in relation to a number of other applications. For example, the system may be used to ablate tissue causing atrial fibrillation or flutter, tumors, or for coagulation treatment.

The programmable controller 2 may be implemented using a general purpose computer executing a control algorithm to operate the RF splitter 8 in response to measured temperamres of the electrodes 22 A to 22D, as described below. In this embodiment, the programmable controller 2 is preferably implemented using an AMLAB instrument emulator (published in International Publication No. WO92/ 15959 on 17 September 1992; International Application No. PCT/AU92/00076), which comprises a general purpose computer having a digital signal processor subassembly that is configurable using a graphical compiler. The programmable controller 2 is connected to the N-channel RF splitter 6 via N output control signals 14 and N temperamre signals 16 provided from the N-channel RF splitter 6 to the programmable controller 2. The N-channel RF splitter 6, the RF generator 8, the RMS-to-DC converter 10, the probe 20, and the dispersive plate 12, shown as module 4, are provided so as to meet electrical isolation barrier requirements in accordance with IEC 601 and AS3200.1 type CF standards.

The N-channel RF splitter 6 provides RF energy from the RF generator 8 coupled to the splitter 6 via N electrical connections 18 to the corresponding electrodes 22 A to 22D of the probe 20. In addition, the N electrical connections 18 are connected to corresponding thermocouples of each of the electrodes 22A to 22D. While thermocouples are preferably employed, other temperamre transducers or sensing circuits/devices may be practiced without departing from the scope and spirit of the invention. For example, a temperamre sensing device for a respective electrode of one or more electrodes could include a thermistor or other temperamre transducer. The N temperature signals 16 provided to the programmable controller 2 are obtained from the temperamre sensing devices of the electrodes 22A to 22D. The RF generator 8 is also connected to the dispersive electrode 12 via the RMS-to-DC converter 10.

This embodiment advantageously employs a single RF generator in which the N-channel RF splitter 6 independently controls the delivery of RF energy of a single phase to one or more of the electrodes 22 A to 22D of the probe 20. The temperamre of each of the electrodes 22A to 22D is independently monitored by the programmable controller 2, which in turn provides the control signals 14 to the N-channel RF splitter 6 to simultaneously control the amount of RF energy delivered to the corresponding electrode 22 A to 22D.

Using closed-loop feedback and independent, simultaneous control of each electrode, the system is able to advantageously regulate temperamres to occur at each electrode at the desired temperamre. This produces optimum lesion size, and avoids charring and vaporisation associated with temperamres greater than 100°C. This is in marked contrast to the prior art, since the embodiment provides a margin of at least 20° C, highlighting the lack of temperamre control of all of the electrodes in the conventional system. The prior art is able to affect only the temperamre of the electrode being monitored. As lesions size is proportional to the temperamre of the electrodes, the system according to this embodiment is able to controllably produce larger lesion. The ability to maintain all electrodes at a desired temperamre simultaneously and independently enables contiguous uniform lesions, not as dependent on the size and contact area of each electrode. Conversely, if it is desired to deliver RF energy to only one particular electrode to minimise thermal damage to "good" tissue, the system according to this embodiment is able to ensure that adjacent electrodes have minimal current. That is, the system according to this embodiment has the ability to ensure precise temperamre control of each electrode individually and simultaneously. Fig. 3 is a detailed schematic diagram of the system of Fig. 1. As shown in Fig. 3, the number of electrodes and separate channels N is preferably four (4). However, this embodiment may be practiced with a different number (e.g., N = 3 or _ _

N = 5) of electrodes and channels without departing from the scope and spirit of the present invention. Further, the splitter may be practiced with N channels and a number of separate probes where the total number of electrodes of the probes is less than or equal to N. A single electrode 22A and corresponding channel of the N-channel RF splitter 6 is described hereinafter with reference to Fig. 2. While a single electrode 22A and corresponding channel are described, it will be apparent to a person skilled in the art that the following description applies equally to the three remaining electrodes 22B to 22D and the corresponding channels of the splitter of Fig. 3.

In Fig. 2, the control signal 14A output by the programmable controller 2 is provided to an isolation amplifier 42 A which in turn is connected to a fast-switching, full bridge rectifier 34A. In particular, the output of the isolation amplifier 42A is connected to a fast-switching variable resistance 48A used to control operation of the rectifier bridge 34A. Preferably, the variable resistance 48A is implemented using a power N-channel enhancement MOSFET. The programmable controller 2 receives a temperamre signal 16A from the output of another isolation amplifier 40A.

One terminal of the RF generator 8 is coupled via a decoupling capacitor 9 to the dispersive electrode 12. The tissue (e.g. , myocardium) which the probe 20 is to be applied to is generally represented by a block 15 between the dispersive plate 12 and an electrode 22 A of the needle probe 20. In this embodiment, the needle probe is inserted into the tissue. The electrode 22A is generally represented by a mbular or ring-like structure in accordance with the electrode structure employed in the needle probe 20. However, again it will be appreciated that other electrode structures may be practised dependent on the probe type without departing from the scope and spirit of the invention. The other terminal of the RF generator 8 is connected via a fail-safe relay 38A and a thermal fuse, current limiter 39A to the rectifier bridge 34A. The relay 38A consists of a fail-safe relay contact 38A' and a fail-safe relay winding 38A' ' . These circuits act as current interrupting and current limiting devices.

The output terminal of the fast-switching, full bridge rectifier 34A is coupled via a decoupling impedance matching capacitor 44A to a stainless steel conductor 47A, ^ ₂

which is connected to the stainless steel electrode 22A and a terminal of the thermocouple junction 36A. The stainless steel conductor 47A is also connected to a low pass filter 30A, preferably composed of passive elements. A titanium conductor 46A is also coupled to the stainless steel electrode 22A and the other terminal of the thermocouple junction 36A embedded in the electrode 22A. The titanium conductor 46A is further connected to the low-pass filter 30A. However, other conductive materials may be used for the electrode 22A and the conductors 46A and 47A without departing from the scope and spirit of the invention. The output of the low pass filter 30A is provided to a thermocouple reference compensation amplifier and alarm 32A. The amplifier 32A also provides a control signal to the relay 38A. The output of the amplifier 32A is provided to the isolation amplifier 40A, which in turn provides the temperamre signal 16A to the programmable controller 2. Again, other temperamre sensing devices and corresponding associated circuits to provide equivalent functionality may be practiced without departing from the scope and spirit of the invention.

The thermocouple 36A embedded in the electrode 22A produces a temperamre signal on conductors 46A and 47A in response to the heat produced by the delivery of RF energy to the myocardium tissue 15. The signal produced by the thermocouple junction 36A is low-pass filtered using the low-pass filter 30A, the output of which is provided to the amplifier and alarm 32A. The alarm and amplifier 32A produces an amplified temperamre signal that is provided to the isolation amplifier 40A. In addition, the amplifier and alarm 32A provides a control signal to operate the relay 38A so as to interrupt the delivery of RF energy from the RF generator via the relay 38A when the measured or sensed temperature exceeds a predetermined threshold level. The programmable controller 2 uses the temperamre signal 16A to produce a control signal 14A that is provided to the variable resistance 48A of the full bridge rectifier 34A. This control signal 14A is provided via the isolation amplifier 42 A. The control signal 14A operates the full bridge rectifier so as to variably and continuously control the amount of RF energy delivered to the stainless steel electrode 22A for ablation. Thus, this embodiment is able to precisely and independently control the electrodes 22A to 22D of the needle probe 20.

The heating in RF energy transfer occurs not from the electrode 22A to 22D itself but from a small volume of tissue in contact with the electrode 22 A to 22D. This heating source is directly proportional to the electrode surface area in contact with the tissue, contact pressure and the electrical conductivity of the tissue. Therefore, the system according to this embodiment advantageously controls the RF energy in each electrode independently of each other.

Thus, the system provides maximum control at each electrode 22A to 22D by minimising current flow between adjacent electrodes 22 A to 22D. This is achieved by a single RF source (one phase) 8 using RF splitter 8 to regulate current flow to each electrode 22 A to 22D as a function of the temperamre of each electrode.

The first embodiment illustrated in Figs. 1 to 3 provides a system for simultaneous unipolar, multi-electrode ablation using simultaneous closed-loop control of temperamre at each electrode 22 A to 22D. This system advantageously enables multi-electrode ablation for ablating ventricular tachycardia and atrial fibrillation. In contrast to conventional ablation systems which cut off current to any electrode during ablation if a temperamre or impedance goes above a particular level and therefore cannot produce reliable lesions because the electrode-tissue interface surface area varies considerably during ablation, this embodiment is able to overcome this disadvantage of conventional systems. In this embodiment, the control algorithm for generating the control signals and operating the system in response to the temperamre of each of the electrodes is preferably implemented in software carried out using a general purpose computer. An experimental example of the use of the system is set forth below outlining the use of another system in accordance with that of this embodiment. - -

EXAMPLE

A system in accordance with the first embodiment was implemented and tested to compare unipolar versus bipolar ablation and single electrode temperamre control versus simultaneous multi-electrode temperamre control during ablation. Two types of 21 gauge needles, each with 2 cylindrical electrodes were introduced from the epicardium at thoracotomy in 3 greyhounds. The proximal electrode measured 1mm. The distal electrode measured 1mm in one needle and 1.5mm in the other. The inter electrode distance was 4mm. Seventy four intramural RF ablations were performed for 60 seconds through both the electrodes of each needle simultaneously in an unipolar (Uni) or a bipolar (Bi) fashion. During ablations the temperamre of only one electrode (proximal or distal) or both the electrodes simultaneously were maintained at 80°C by closed loop control. Lesion sizes were measured histologically.

The maximum _+ SD temperamre (temp) measured at the proximal (P) and the distal (D) electrodes were:

(electrode controlled = electrode at which temperamre was controlled)

Length of each Uni Electrode Temp of P Temp of D p value electrode in needle or Bi controlled electrode electrode

P = 1 mm, D = 1 mm Bi P(l mm) 82 i l 82 ± 2 0.7

P = 1 mm, D = 1 mm Uni P(l mm) 83 ± l 82 ± 2 0.01

P = 1 mm, D = 1.5 mm Bi P(l mm) 81 ± 1 60 ± 2 <0.001

P = 1 mm, D = 1.5 mm Bi D(1.5 mm) 96 ± 2 80 ± 2 < 0.001

P = 1 mm, D = 1.5 mm Uni Both 82 ± 2 81 ± l 0.24 Simultaneous multi-electrode ablation without closed-loop temperamre control of each electrode results in higher temperamre at the smaller electrode-tissue interface and lower temperamre at the larger electrode-tissue interface. This results in varying lesion sizes and potentially coagulum formation and impedance rises. Unipolar RF ablation with simultaneous closed-loop temperamre control of each electrode is the optimum method for simultaneous multi-electrode ablation.

Second Embodiment Another embodiment of the invention is illustrated in Fig. 4, in which like elements of Figs. 1 to 3 are indicated with the same reference numerals. For the purpose of brevity only, components of the second embodiment shared with the first embodiment are not repeated hereinafter. However, those aspects of the second embodiment will be readily understood by a person skilled in the art in view of the description with reference to Figs. 1 to 3. Instead, the description hereinafter describes those aspects of the second embodiment not set forth above.

A single channel of the system according to the second embodiment is shown schematically in Fig. 4. The system comprises the programmable controller 2 and the module 4' , which comprises the like numbered elements of Fig. 2, a voltage/current sensing module 50A and the corresponding isolation amplifier 52A. Again, while the RF generator 8 is illustrated within the module 4' , it will be apparent to a person skilled in the art that the RF generator 8 can be equally applied to plural channels, as indicated in Fig. 3.

The conductors 46A and 47A are also coupled to the input terminals of the voltage and/or current sensing module 50A, which preferably detects the root-mean- square (RMS) voltage and/or current at the electrode 22A. The detected or measured voltage and/or current signal is output by the sensing module 50A and provided to isolation amplifier 52A. In turn the output of the isolation amplifier 52A is provided to the programmable controller 2. The voltage and/or current sensing module 50A measures the RMS voltage and current delivered to the electrode 22A. Thus, the average power and impedance of each electrode 22 A can be determined independently as well. Thus, the module 50A independently senses at least one of following: the voltage, current, impedance and average power of each electrode. This is done to provide a corresponding measurement signal which can be used by the programmable controller so that additional safety features may be implemented in the system. This preferably provides an increased level of safety by enabling predetermined cut-off levels (eg, RMS voltage, RMS current, impedance and average power) to be used to shut-down the output of each electrode 22 A. This is preferably carried out by the programmable controller 2 which provides control signal 14A dependent upon at least one of these criteria. Thus, the controller 2 generates the control signal 14A to independently interrupt delivery of the RF energy to the respective electrode when the meaurement signal exceeds a predetermined threshold condition. Further control structures utilising RMS voltage and/or current may also be applied to enhance the control and safety performance of the system.

Thus, the second embodiment provides, in addition to the advantages of the first embodiment, additional safety features.

While only a small number of embodiments of the invention has been described, it will be apparent to a person skilled in the art that modifications and changes thereto can be made without departing from the scope and spirit of the present invention.

Claims

1. A system for ablating tissue, comprising: means for generating RF energy; probe means comprising N separate electrodes, each having a corresponding means for sensing the temperamre of said electrode; splitter means for splitting said RF energy coupled to said generating means and said probe means, said splitter means having N separate channels each being coupled to a corresponding one of said N electrodes and temperamre sensing means; and means for controlling said splitter means, whereby the ablation of tissue at each electrode is independently controlled using closed loop feedback of the temperature of said electrode by independently regulating the amount of said RF energy delivered to each electrode.

2. The system according to claim 1 , comprising a plurality of probe means and splitter means, wherein said controlling means separately controls each of said probe means and said corresponding splitter means.

3. The system according to claim 1 or 2, wherein said probe means has an elongated needle-like structure with one end adapted to puncture tissue and having sufficient rigidity to puncture said tissue, wherein each of said electrodes consists of a metal substantially circular surface separated one from another by insulation means.

4. The system according to claim 1 or 2, wherein said probe means is a catheter probe device.

5. The system according to any one of claims 1 to 4 wherein said RF energy has a single phase.

6. The system according to any one of claims 1 to 5, further comprising means for independently and continuously adjusting said RF energy delivered to each electrode in response to a control signal from said controlling means dependent on said temperamre of said electrode.

7. The system according to any one of claims 1 to 6, wherein said controlling means is programmable.

8. The system according to any one of claims 1 to 7 wherein each respective temperamre sensing means comprises a thermocouple.

9. The system according to any one of claims 1 to 8, wherein said splitter means comprises means for independently interrupting current from said RF energy generating means to one or more of said electrodes.

10. The system according to any one of claims 1 to 9, further comprising means for independently sensing at least one of the group consisting of the voltage, current, impedance and average power of each electrode to provide a corresponding measurement signal; and wherein said controlling means generates said control signal to independently interrupt delivery of said RF energy to said respective electrode when said meaurement signal exceeds a predetermined threshold condition.

11. A medical apparams for treatment by radiofrequency (RF) ablation of tissue, said apparams comprising: an RF energy generator; one or more probes each comprising a plurality of separate electrodes and corresponding temperamre sensors for sensing the temperamre of said electrodes, each temperamre sensor connected to a respective one of said plurality of electrodes; a splitter for splitting said RF energy provided by said RF energy generator, said splitter having a plurality of separate channels, wherein each of said electrodes is coupled to a respective one of said plurality of channels; and a programmable controller coupled to said RF splitter for independently controlling the ablation of tissue at each electrode using closed loop feedback of the temperamre of said electrode, whereby the amount of said RF energy delivered to each electrode is independently regulated by said programmable controller. - -

12. The medical apparams according to claim 11 , comprising at least two probes, and wherein said programmable controller separately controls each of said probes.

13. The medical apparams according to claim 11 or 12, wherein each probe has an elongated needle-like strucmre with one end adapted to puncmre tissue and having sufficient rigidity to puncmre said tissue, wherein each of said electrodes consists of metal separated one from another by insulative material.

14. The medical apparams according to any one of claims 11 to 13 wherein said RF energy has a single phase.

15. The medical apparams according to any one of claims 11 to 14, further comprising means for independently and continuously adjusting said RF energy delivered to each electrode in response to said programmable controller dependent on said temperamre of said electrode.

16. The medical apparams according to claim 11 or 12 wherein each probe is a catheter device.

17. The medical apparams according to any one of claims 11 to 16, wherein each of said temperamre sensors comprises a temperamre transducer.

18. The medical apparams according to claim 17 wherein said temperamre transducer is a thermocouple at least partially embedded in said respective electrode.

19. The medical apparams according to any one of claims 11 to 18 wherein each channel of said splitter is coupled to means for interrupting current delivered to the corresponding electrode.

20. The medical apparams according to any one of claims 11 to 19 comprising means for independently interrupting the delivery of RF energy to each electrode when at least one of the voltage, current, impedance and average power measured at the respective electrode exceeds a predetermined threshold.

21. A radio frequency (RF) energy splitter for use with one or more probes in a system for RF ablation of tissue, each probe comprising a plurality of separate electrodes and corresponding temperature sensors for sensing the temperamre of said electrode, said splitter comprising: input means for receiving RF energy from an RF energy generator; a plurality of channel modules for separately delivering RF energy from said input means to a respective electrode of said plurality of electrodes of said one or more probes, each channel module comprising: means for variably adjusting an amount of said RF energy delivered to said respective electrode in response to a control signal, said variable adjusting means being coupled between said input means and said respective electrode; means for interrupting said RF energy delivered to said respective electrode; output means coupled to said respective temperamre sensor for providing a temperamre signal; means for determining if said temperamre at said respective electrode exceeds a predetermined threshold and actuating said interrupting means if said threshold is exceeded, whereby said RF energy is interrupted from delivery to said respective electrode; wherein each channel module is capable of receiving said respective control signal from and providing said respective temperamre signal to a programmable controller so that the amount of said RF energy delivered to each electrode can be independently regulated using closed loop feedback of the temperamre of each electrode.

22. The splitter according to claim 21, wherein said variable adjusting means comprises a bridge rectifier including a fast-switching variable resistance for controlling operation of said bridge rectifier in response to said control signal.

23. The splitter according to claim 21 or 22, wherein said RF energy interrupting means comprises means for interrupting a current through said RF energy interrupting means and means for limiting said current.

24. The splitter according to any one of claims 21 to 23, wherein said determining means compares said temperamre signal with said predetermined threshold.

25. The splitter according to any one of claims 21 to 24 wherein said one or more probes each has a needle-like strucmre with one end adapted to puncmre tissue and having sufficient rigidity to puncmre said tissue, wherein each of said electrodes conceits of metal separated one from another by insulative material.

26. The splitter according to any one of claims 21 to 25 wherein said one or more probes each comprise a catheter probe device.

27. The splitter according to any one of claims 21 to 25, wherein each channel comprises means for sensing at least one of the group consisting of the voltage, current, impedance and average power of said respective electrode whereby said programmable controller can interrupt delivery of said RF energy to said electrode dependent upon the measurement provided by said sensing means.

28. A method for ablating tissue, comprising the steps of: generating RF energy; providing probe means comprising N separate electrodes, each having a corresponding means for sensing temperature of said electrode; sensing the temperamre of each electrode using said temperamre sensing means of said electrode; splitting said RF energy to said probe means into N separate channels each being coupled to a corresponding one of said N electrodes and said temperamre sensing means; and controlling the splitting of said RF energy to said probe means, whereby the ablation of tissue at each electrode is independently controlled using closed loop feedback of the measured temperature of said electrode by independently regulating the amount of said RF energy delivered to each electrode.

29. The method according to claim 28, further comprising the step of separately controlling the splitting of said RF energy to a plurality of said probe means.

30. The method according to claims 28 or 29, wherein said probe means has an elongated needle-like strucmre with one end adapted to puncmre tissue and having sufficient rigidity to puncmre said tissue, wherein each of said electrodes consists of a metal substantially circular surface separated one from another by

5 insulation means.

31. The method according to any one of claims 28 to 30 wherein said RF energy has a single phase.

32. The method according to any one of claims 28 to 31, further comprising the step of independently and continuously adjusting said RF energy i o delivered to each electrode in response to a control signal from a programmable controlling means dependent on said temperature of said electrode.

33. The method according to any one of claims 28 to 32, further comprising the steps of: sensing at least one of the group consisting of the voltage, current, impedance 15 and average power of the respective electrode; and independently interrupting the delivery of said RF energy to said electrode if a predetermined threshold is exceeded by the sensed value.

34. A method for treatment by radiofrequency (RF) ablation of tissue, said method comprising the steps of:

20 generating RF energy; providing one or more probes each comprising a plurality of separate electrodes and corresponding temperamre sensors, each temperamre sensor connected to a respective one of said plurality of electrodes; measuring the temperamre of each electrode using said respective temperamre 25 sensor; splitting said RF energy into a plurality of separate channels, wherein each of said electrodes is coupled to a respective one of said plurality of channels; and programmably controlling the splitting of said RF energy so as to independently control the ablation of tissue at each electrode using closed loop feedback of the measured temperamre of said electrode, whereby the amount of said RF energy delivered to each electrode is independently regulated.

35. The method according to claim 34, comprising the further steps of using at least two probes, and programmably controlling each of said probes separately.

36. The method according to claims 34 or 35, wherein each probe has an elongated needle-like strucmre with one end adapted to puncmre tissue and having sufficient rigidity to puncmre said tissue, wherein each of said electrodes consists of metal separated one from another by insulative material.

37. The method according to any one of claims 34 to 36 wherein said RF energy has a single phase.

38. The method according to any one of claims 34 to 37, further comprising the step of independently and continuously adjusting said RF energy delivered to each electrode in response to said temperamre of said electrode.

39. The method according to any one of claims 34 to 38, further comprising the step of independently interrupting the delivery of RF energy to each electrode when at least one of the voltage, current, impedance and average power measurement at the respective electrode exceeds a predetermined threshold.

40. A method of splitting radio frequency (RF) energy delivered to one or more probes in a system for RF ablation of tissue, each probe comprising a plurality of separate electrodes and corresponding temperamre sensors for sensing the temperamre of said electrode, said method comprising the steps of: receiving RF energy from an RF energy generator; providing a plurality of channel modules for separately delivering said RF energy to a respective electrode of said plurality of electrodes of said one or more probes, further comprising, for each channel module, the sub-steps of: variably adjusting an amount of said RF energy delivered to said respective electrode in response to a control signal; measuring the temperamre of said respective electrode using said corresponding temperamre sensor to provide a temperamre signal; determining if said temperamre at said respective electrode exceeds a predetermined threshold and interrupting delivery of said RF energy to said respective electrode if said threshold is exceeded; wherein each channel module is capable of receiving said respective control signal from and providing said respective temperamre signal to a programmable controller so that the amount of said RF energy delivered to each electrode can be independently regulated using closed loop feedback of the temperamre of each electrode.

41. The method according to claim 40, wherein said step of variably adjusting said RF energy comprises the step of changing the resistance of a fast- switching variable resistance incorporated in a bridge rectifier in response to said control signal.

42. The method according to claim 40 or 41 , wherein said step of interrupting said RF energy comprises the steps of interrupting a current to said respective electrode and limiting said current.

43. The method according to any one of claims 40 to 42, wherein said step of determining comprises the step of comparing said temperamre signal with said predetermined threshold.

44. The method according to any one of claims 40 to 42, for each channel module, further comprises the sub-steps of: sensing at least one of the group consisting of the voltage, current, impedance and average power of said respective electrode; and independently interrupting delivery of said RF energy to said electrode dependent upon the sensed value.