US 6,090,106 AGrant

Electrosurgical Instrument

Issue Date:2000-07-18

•20 Claims

•11 Drawing Sheets

Abstract

An electrosurgical instrument is disclosed for the treatment of tissue in the presence of an electrically-conductive fluid. The instrument comprises an instrument shaft, and a tissue treatment electrode at one end of the shaft, the tissue treatment electrode being constructed to define thermal barriers for limiting thermal conduction therealong, thereby to encourage the formation and maintenance of a layer of vapor over the electrode.

Metadata

Assignee

Gyrus Medical Limited

Inventors

Nigel Mark Goble
Colin Charles Owen Goble

Application Information

Application Number:US 048718&

Filing Date:1998-03-26

Priority Date:1996-01-09

Art Unit:379

Classifications

IPC:

A61B 1818

Field of Search:

60660760441;42;45-50100-105;115;11621;22;114

Patent Drawings (11 sheets)

Description

Background of the Invention

This invention relates to an electrosurgical instrument for the treatment of tissue in the presence of an electrically conductive fluid medium, to electrosurgical apparatus including such an instrument, and to an electrode unit for use in such an instrument.

Endoscopic electrosurgery is useful for treating tissue in cavities of the body, and is normally performed in the presence of a distension medium. When the distension medium is a liquid, this is commonly referred to as underwater electrosurgery, this term denoting electrosurgery in which living tissue is treated using an electrosurgical instrument with a treatment electrode or electrodes immersed in liquid at the operation site. A gaseous medium is commonly employed when endoscopic surgery is performed in a distensible body cavity of larger potential volume in which a liquid medium would be unsuitable, as is often the case in laparoscopic or gastroenterological surgery.

Underwater surgery is commonly performed using endoscopic techniques, in which the endoscope itself may provide a conduit (commonly referred to as a working channel) for the passage of an electrode. Alternatively, the endoscope may be specifically adapted (as a resectoscope) to include means for mounting an electrode, or the electrode may be introduced into a body cavity via a separate access means at an angle with respect to the endoscope--a technique commonly referred to as triangulation. These variations in technique can be subdivided by surgical speciality, where one or other of the techniques has particular advantages given the access route to the specific body cavity. Endoscopes with integral working channels, or those characterised as resectoscopes, are generally employed when the body cavity may be accessed through a natural body opening--such as the cervical canal to access the endometrial cavity of the uterus, or the urethra to access the prostate gland and the bladder. Endoscopes specifically designed for use in the endometrial cavity are referred to as hysterocopes, and those designed for use in the urinary tract include cystoscopes, urethroscopes and resectoscopes. The procedures of transurethal resection or vaporisation of the prostrate gland are known as TURP and EVAP respectively. When there is no natural body opening through which an endoscope may be passed, the technique of triangulation is commonly employed. Triangulation is commonly used during underwater endoscopic surgery on joint cavities such as the knee and the shoulder. The endoscope used in these procedures is commonly referred to an as arthroscope.

Electrosurgery is usually carried out using either a monopolar instrument or a bipolar instrument. With monopolar electrosurgery, an active electrode is used in the operating region, and a conductive return plate is secured to the patient's skin. With this arrangement, current passes from the active electrode through the patient's tissues to the external return plate. Since the patient represents a significant portion of the circuit, input power levels have to be high (typically 150 to 250 watts), to compensate for the resistive current limiting of the patient's tissues and, in the case of underwater electrosurgery, power losses due to the fluid medium which is rendered partially conductive by the presence of blood or other body fluids. Using high power with a monopolar arrangement is also hazardous, due to the tissue heating that occurs at the return plate, which can cause severe skin burns. There is also the risk of capacitive coupling between the instrument and patient tissues at the entry point into the body cavity.

With bipolar electrosurgery, a pair of electrodes (an active electrode and a return electrode) are used together at the tissue application site. This arrangement has advantages from the safety standpoint, due to the relative proximity of the two electrodes so that radio frequency currents are limited to the region between the electrodes. However, the depth of effect is directly related to the distance between the two electrodes; and, in applications requiring very small electrodes, the inter-electrode spacing becomes very small, thereby limiting tissue effect and the output power. Spacing the electrodes further apart would often obscure vision of the application site, and would require a modification in surgical technique to ensure correct contact of both electrodes with the tissue.

There are a number of variations to the basic design of the bipolar probe. For example, U.S. Pat. No. 4,706,667 describes one of the fundamentals of the design, namely that the ratio of the contact areas of the return electrode and of the active electrode is greater than 7:1 and smaller than 20:1 for cutting purposes. This range relates only to cutting electrode configurations. When a bipolar instrument is used for desiccation or coagulation, the ratio of the contact areas of the two electrodes may be reduced to approximately 1:1 to avoid differential electrical stresses occurring at the contact between the tissue and the electrodes.

The electrical junction between the return electrode and tissue can be supported by wetting of the tissue by a conductive solution such as normal saline. This ensures that the surgical effect is limited to the needle or active electrode, with the electric circuit between the two electrodes being completed by the tissue. One of the obvious limitations with the design is that the needle must be completely buried in the tissue to enable the return electrode to complete the circuit. Another problem is one of the orientation: even a relatively small change in application angle from the ideal perpendicular contact with respect to the tissue surface, will change the contact area ratio, so that a surgical effect can occur in the tissue in contact with the return electrode.

Cavity distension provides space for gaining access to the operation site, to improve visualisation, and to allow for manipulation of instruments. In low volume body cavities, particularly where it is desirable to distend the cavity under higher pressure, liquid rather than gas is more commonly used due to better optical characteristics, and because it washes blood away from the operative site.

Conventional underwater electrosurgery has been performed using a non-conductive liquid (such as 1.5% glycine) as an irrigant, or as a distension medium to eliminate electrical conduction losses. Glycine is used in isotonic concentrations to prevent osmotic changes in the blood when intra-vascular absorption occurs. In the course of an operation, veins may be severed, with resultant infusion of the liquid into the circulation, which could cause, among other things, a dilution of serum sodium which can lead to a condition known as water intoxication.

The applicants have found that it is possible to use a conductive liquid medium, such as normal saline, in underwater endoscopic electrosurgery in place of non-conductive, electrolyte-free solutions. Normal saline is the preferred distension medium in underwater endoscopic surgery when electrosurgery is not contemplated, or a non-electrical tissue effect such as laser treatment is being used. Although normal saline (0.9% w/v; 150 mmol/l) has an electrical conductivity somewhat greater than that of most body tissue, it has the advantage that displacement by absorption or extravasation from the operative site produces little physiological effect, and the so-called water intoxication effects of non-conductive, electrolyte-free solutions are avoided.

The applicants have developed a bipolar instrument suitable for underwater electrosurgery using a conductive liquid or gaseous medium. This electrosurgical instrument for the treatment of tissue in the presence of a fluid medium, comprises an instrument body having a handpiece and an instrument shaft and an electrode assembly, at one end of the shaft. The electrode assembly comprises a tissue treatment electrode which is exposed at the extreme distal end of the instrument, and a return electrode which is electrically insulated from the tissue treatment electrode and has a fluid contact surface spaced proximally from the exposed part of the tissue treatment electrode. In use of the instrument, the tissue treatment electrode is applied to the tissue to be treated whilst the return electrode, being spaced proximally from the exposed part of the tissue treatment electrode, is normally spaced from the tissue and serves to complete an electrosurgical current loop from the tissue treatment electrode through the tissue and the fluid medium. This electrosurgical instrument is described in the specification of the applicants' co-pending International Patent Application No. PCT/GB96/01473, the contents of which are incorporated in this application by reference.

The electrode structure of this instrument, in combination with an electrically conductive fluid medium largely avoids the problems experienced with monopolar or bipolar electrosurgery. In particular, input power levels are much lower than those generally necessary with a monopolar arrangement (typically 100 watts). Moreover, because of the relatively large spacing between its electrodes, an improved depth of effect is obtained compared with a conventional bipolar arrangement.

FIG. 1 illustrates the use of this type of instrument for tissue removal by vaporisation. The electrode assembly 12 of this instrument comprises a tissue treatment (active) electrode 14 which is exposed at the distal end of the instrument, and a return electrode which is spaced from the exposed part of the tissue treatment electrode by an insulation sleeve 16. This electrode assembly is powered to create a sufficiently high energy density at the tissue treatment electrode 14 to vaporise tissue 22, and to create a vapour pocket 24 surrounding the active tip. The formation of the vapour pocket 24 creates about a 10-fold increase in contact impedance, with a consequent increase in output voltage. Arcs 26 are created in the vapour pocket 24 to complete the circuit to the return electrode 18. Tissue 22 which contacts the vapour pocket 24 will represent a path of least electrical resistance to complete the circuit. The closer the tissue 22 comes to the electrode 14 the more energy is concentrated to the tissue, to the extent that the cells explode as they are struck by the arcs 26, because the return path through the conductive fluid (saline in this case) is blocked by the high impedance barrier of the vapour pocket 24. The saline solution also acts to dissolve the solid products of vaporisation.

The power threshold required to reach vaporisation is an important parameter of this type of instrument, and it is the aim of the invention to provide a bipolar electrosurgical instrument having improved vaporisation power threshold properties.

Summary of the Invention

In its broadest aspect, the invention provides an electrosurgical instrument having an electrode which is so constructed as to have a better vaporisation power threshold than known electrodes.

The present invention provides an electrosurgical system for the vaporisation of tissue in the presence of an electrically-conductive medium, the system comprising an electrosurgical generator for generating radio frequency power, and an electrosurgical instrument connectible to the generator, wherein he generator has a radio frequency output stage for delivering radio frequency power to a pair of output connections, which output stage has an open loop output impedance of less than 250 ohms; the electrosurgical instrument comprises an instrument shaft and, situated at a distal end of the shaft, an electrode assembly comprising an active electrode with an exposed treatment portion and a return electrode with an exposed fluid contact surface, the fluid contact surface being set back from the treatment portion so that, when the electrode assembly is brought into an operative position with the treatment portion on or adjacent to the surface of the tissue to be treated, the fluid contact surface is further from the tissue surface than the treatment portion; and the ratio of the surface area of the exposed treatment portion to the surface area of the exposed fluid contact surface is greater than or equal to 0.5 to 1; the electrode assembly further comprising means associated with the active electrode for hindering the dissipation of heat from the active electrode to its surroundings, thereby to encourage the formation and maintenance of a layer of vapour over its surface.

The invention also provides an electrosurgical instrument for the treatment of tissue in the presence of an electrically-conductive fluid medium, the instrument comprising an instrument shaft and an electrode assembly at a distal end of the shaft, wherein the electrode assembly comprises:

a single active electrode having an exposed tissue treatment portion;

a return electrode having an exposed fluid contact surface; and

an insulating member positioned between and electrically insulating the active electrode and the return electrode, and serving to space apart the exposed treatment portion of the active electrode and the exposed fluid contact surface of the return electrode, the fluid contact surface of the return electrode being set back in the direction of a treatment axis of the assembly from the active electrode exposed treatment portion; and wherein the ratio of the area of the exposed treatment portion to the area of the exposed fluid contact surface is greater than or equal to 0.5 to 1; and the active electrode is constituted by a singled coiled filament which defines a generally tubular member, adjacent turns of the coiled filament defining indentations in said generally tubular member, said indentations constituting thermal barriers for limiting thermal conduction along said generally tubular member, whereby, in use, application of sufficient radio frequency power to the electrode assembly vaporises the conductive fluid medium adjacent to the tissue treatment portion to create a stable vapour pocket around the tissue treatment portion.

The invention further provides an electrosurgical instrument for the treatment of tissue in the presence of an electrically-conductive fluid medium, the instrument comprising an instrument shaft and an electrode assembly at a distal end of the shaft, wherein the electrode assembly comprises:

a single active electrode having an exposed tissue treatment portion;

a return electrode having an exposed fluid contact surface; and

an insulating member positioned between and electrically insulating the active electrode and the return electrode, and serving to space apart the exposed treatment portion of the active electrode and the exposed fluid contact surface of the return electrode, the fluid contact surface of the return electrode being set back in the direction of a treatment axis of the assembly from the active electrode exposed treatment portion; and wherein the ratio of the area of the exposed treatment portion, to the area of the exposed fluid contact surface is greater than or equal to 0.5 to 1; and the active electrode is configured to define thermal barriers for limiting thermal conduction therealong, whereby, in use, application of sufficient radio frequency power to the electrode assembly vaporises the conductive fluid medium adjacent to the tissue treatment portion to create a stable vapour pocket around the tissue treatment portion.

The electrosurgical instrument of the invention is useful for dissection, resection, vaporisation, desiccation and coagulation of tissue and combinations of these functions with particular application in hysteroscopic surgical procedures. Hysteroscopic operative procedures may include: removal of submucosal fibroids, polyps and malignant neoplasms; resection of congenital uterine anomalys such as a septum or subseptum; division of synechiae (adhesiolys is); ablation of diseased or hypertrophic endometrial tissue; and haemostasis.

The instrument of the invention is also useful for dissection, resection, vaporisation, desiccation and coagulation of tissue and combinations of these functions with particular application in arthroscopic surgery as it pertains to endoscopic and percutaneous procedures performed on joints of the body including, but not limited to, such techniques as they apply to the spine and other non-synovial joints. Arthroscopic operative procedures may include: partial or complete meniscectomy of the knee joint including meniscal cystectomy; lateral retinacular release of the knee joint; removal of anterior and posterior cruciate ligaments or remnants thereof; labral tear resection, acromioplasty, bursectomy and subacromial decompression of the shoulder joint; anterior release of the temperomandibular joint; synovectomy, cartilage debridement, chondroplasty, division of intra-articular adhesions, fracture and tendon debridement as applied to any of the synovial joints of the body; inducing thermal shrinkage of joint capsules as a treatment for recurrent dislocation, subluxation or repetitive stress injury to any articulated joint of the body; discectomy either in the treatment of disc prolapse or as part of a spinal fusion via a posterior or anterior approach to the cervical, thoracic and lumbar spine or any other fibrous joint for similar purposes; excision of diseased tissue; and haemostasis.

The instrument of the invention is also useful for dissection, resection, vaporisation, desiccation and coagulation of tissue and combinations of these functions with particular application in urological endoscopic (urethroscopy, cystoscopy, ureteroscopy and nephroscopy) and percutaneous surgery. Urological procedures may include: electro-vaporisation of the prostrate gland (EVAP) and other variants of the procedure commonly referred to as transurethral resection of the prostate (TURP) including, but not limited to, interstitial ablation of the prostate gland by a percutaneous or perurethral route whether performed for benign or malignant disease; transurethral or percutaneous resection of urinary tract tumours as they may arise as primary or secondary neoplasms, and further as they may arise anywhere in the urological tract from the calyces of the kidney to the external urethral meatus; division of strictures as they may arise at the pelviureteric junction (PUJ), ureter, ureteral orifice, bladder neck or urethra; correction of ureterocoele shrinkage of bladder diverticular, cystoplasty procedures as they pertain to corrections of voiding dysfunction; thermally induced shrinkage of the pelvic floor as a corrective treatment for bladder neck descent; excision of diseased tissue; and haemostasis.

Surgical procedures using the instrument of the invention include introducing the electrode assembly to the surgical site whether through an artificial conduit (a cannula), or through a natural conduit which may be in an anatomical body cavity or space or one created surgically. The cavity or space may be distended during the procedure using a fluid, or may be naturally held open by anatomical structures. The surgical site may be bathed in a continuous flow of conductive fluid such as saline solution to fill and distend the cavity. The procedures may include simultaneous viewing of the site via an endoscope or using an indirect visualisation means.

The invention also provides an electrode unit for an electrosurgical instrument for the treatment of tissue in the presence of an electrically-conductive fluid medium, the electrode unit comprising a shaft having at one end means for connection to an instrument handpiece, and, mounted on the other end of the shaft, a tissue treatment electrode, the tissue treatment electrode being constructed to define pockets for trapping electrically-conductive fluid and vapour.

The invention further provides an electrode unit for an electrosurgical instrument for the treatment of tissue in the presence of an electrically-conductive fluid medium, the electrode unit comprising a shaft having at one end means for connection to an instrument handpiece, and, mounted on the other end of the shaft, a tissue treatment electrode, the tissue treatment electrode being made from an electrically-conductive material and being coated with a resistive inert material which is effective to increase the local power density within the tissue treatment electrode.

The invention still further provides electrosurgical apparatus comprising a radio frequency generator and an electrosurgical instrument for the treatment of tissue in the pressure of an electrically-conductive fluid medium, the instrument comprising an instrument shaft, and an electrode assembly at one end of the shaft, the electrode assembly comprising a tissue treatment electrode and a return electrode which is electrically insulated from the tissue treatment electrode by means of an insulation member, the tissue treatment electrode being exposed at the distal end portion of the instrument, the return electrode having a fluid contact surface spaced proximally from the exposed end of the tissue treatment electrode by the insulation member, and the radio frequency generator having a bipolar output connected to the electrodes, wherein the exposed end of the tissue treatment electrode is constructed to define a plurality of pockets for trapping electrically-conductive fluid and vapour.

The invention also provides electrosurgical apparatus comprising a radio frequency generator and an electrosurgical instrument for the treatment of tissue in the presence of an electrically-conductive fluid medium, the instrument comprising an instrument shaft, and an electrode assembly at one end of the shaft, the electrode assembly comprising a tissue treatment electrode and a return electrode which is electrically insulated from the tissue treatment electrode by means of an insulation member, the tissue treatment electrode being exposed at the distal end portion of the instrument, the return electrode having a fluid contact surface spaced proximally from the exposed end of the tissue treatment electrode by the insulation member, and the radio frequency generator having a bipolar output connected to the electrodes, wherein the exposed end of the tissue treatment electrode is made from an electrically-conductive material and is coated with a resistive inert material which is effective to increase the local power density within the tissue treatment electrode.

Advantageously, the radio frequency generator includes control means for varying the output power delivered to the electrodes. Preferably, the control means is such as to provide output power in first and second output ranges, the first output range being for powering the electrosurgical instrument for tissue desiccation, and the second output range being for powering the electrosurgical instrument for tissue removal by vaporisation. Conveniently, the first output range is from about 150 volts to 200 volts, and the second output range is from about 250 volts to 600 volts, the voltages being peak voltages.

The invention further provides a method of operating an electrosurgical apparatus having at least a tissue desiccation mode and a tissue vaporisation mode, the apparatus having a radio frequency generator coupled to an electrode assembly for the treatment of tissue in the presence of an electrically-conductive fluid medium, the electrode assembly comprising a tissue treatment electrode and a return electrode which is electrically insulated from the tissue treatment electrode by means of an insulation member, the tissue treatment electrode being exposed at the distal end portion of the assembly, and the return electrode having a fluid contact surface spaced proximally from the exposed end of the tissue electrode by the insulation member, the method comprising the steps of controlling the output power of the radio frequency generator to lie within a first output range for the tissue desiccation mode and to lie within a second output range for the tissue vaporisation mode, the first output range being such that the power supplied to the electrode assembly maintains the conductive fluid adjacent to the tissue treatment electrode substantially at boiling point for tissue desiccation without creating a vapour pocket surrounding the tissue treatment electrode, and the second output range is such that the output power supplied to the electrode assembly for vaporisation of tissue is such as to maintain a vapour pocket surrounding the tissue treatment electrode; and reducing the power threshold for vaporisation at the tissue treatment electrode when the output power of the radio frequency generator is in the second output range.

The invention still further provides an electrosurgical method comprising the steps of: providing an electrosurgical apparatus comprising a radio frequency generator coupled to an electrode assembly comprising a tissue treatment electrode and a return electrode, the tissue treatment electrode being exposed at the distal end portion of the assembly; introducing the electrode assembly into a selected operation site with the tissue treatment electrode adjacent to the tissue to be treated, and with the tissue and the tissue electrode assembly immersed in a conductive liquid; activating the generator; applying sufficient radio frequency power to the electrode assembly to vaporise the conductive liquid surrounding the tissue treatment electrode to maintain a vapour pocket surrounding the tissue treatment electrode; and reducing the power threshold for vaporisation at the tissue treatment electrode.

Brief Description of the Drawings

The invention will now be described in greater detail, by way of example, with reference to the drawings, in which:

FIG. 1 is a diagrammatic side elevation of an electrode unit, showing the use of such a unit for tissue removal by vaporisation;

FIG. 2 is a diagram showing an electrosurgical apparatus constructed in accordance with the invention;

FIG. 3 is a longitudinal sectional view of the distal end of a first form of electrode unit constructed in accordance with the invention;

FIG. 4 is a diagrammatic side elevation of the electrode assembly of a second form of electrode unit constructed in accordance with the invention;

FIG. 5 is a diagrammatic side elevation of a modified electrode assembly similar to that of FIG. 4;

FIG. 6 is a diagrammatic side elevation of the electrode assembly of a third form of electrode unit constructed in accordance with the invention;

FIG. 7 is a diagrammatic side elevation of the electrode assembly of a fourth form of electrode unit constructed in accordance with the invention;

FIG. 8 is a diagrammatic side elevation of the electrode assembly of a fifth form of electrode unit constructed in accordance with the invention;

FIG. 9 is a diagrammatic side elevation of the electrode assembly of a sixth form of electrode unit constructed in accordance with the invention;

FIG. 10 is a diagrammatic side elevation of the electrode assembly of a seventh form of electrode unit constructed in accordance with the invention;

FIGS. 11 and 12 are schematic side elevations of the distal end portion of an electrode assembly similar to that of FIG. 7, showing different stages in the formation of a vapour pocket around conductive electrode filaments;

FIG. 13 is a perspective view of a modified form of the electrode assembly of FIG. 8;

FIG. 14 is a perspective view of part of the assembly of FIG. 13;

FIG. 15 is a cross-section taken on the line A--A of FIG. 13;

FIG. 16 is a graph illustrating the hysteresis of the electrical load impedance and dissipated radio frequency power which occurs during use of an instrument in accordance with the invention in desiccating and vaporising modes;

FIG. 17 is a block diagram of an electrosurgical generator in accordance with the invention;

FIG. 18 is a block diagram of part of the control circuitry of FIG. 17;

FIG. 19 is a waveform diagram showing a typical RF output voltage variation pattern obtained with the generator of FIGS. 17 and 18, the voltage being shown varying with time according to variations in load impedance and generator output stage supply voltage;

FIG. 20 is a graph showing the variation of output power produced by the generator as a function of the load impedance presented to it by the electrode assembly, the output power variation being shown in two operation modes of the generator; and

FIG. 21 is a graph showing the variation of output power produced by the generator as a function of load impedance after modification of the generator characteristics in response to the output voltage sensing.

Detailed Description of the Drawings

Each of the electrode units described below is intended to be used with an electrically conductive fluid medium such as normal saline, and each instrument has a dual-electrode structure, with the conductive medium acting as a conductor between the tissue being treated and one of the electrodes, hereinafter called the return electrode. The other electrode is applied directly to the tissue, and is hereinafter called the tissue treatment active) electrode.

Referring to the drawings, FIG. 2 shows electrosurgical apparatus including a generator 1 having an output socket 2 providing a radio frequency (RF) output for an instrument in the form of a handpiece 3 via a connection cord 4. Activation of the generator 1 may be performed from the handpiece 3 via a control connection in the cord 4, or by means of a foot switch unit 5, as shown, connected separately to the rear of the generator 1 by a foot switch connection cord 6. In the illustrated embodiment, the foot switch unit 5 has two foot switches a and sb. for selecting a desiccation mode and a vaporisation mode of the generator 1 respectively. The generator front panel has push buttons a and b for respectively setting desiccation and vaporisation power levels, which are indicated in a display 8. Push buttons a are provided as an alternative means for selection between the desiccation and vaporisation modes. The handpiece 3 mounts a detachable electrode unit E, such as the electrode units E1 to E9 to be described below.

FIG. 3 shows the distal end of the first form of electrode unit E1 for detachable fastening to the electrosurgical instrument handpiece 3. The electrode unit E1 is formed with an electrode assembly at the distal end thereof, the electrode assembly comprising a central tissue treatment (active) electrode 31 and a tubular return electrode 32. The active electrode 31 is made of a twisted metal such as tungsten, a noble metal such as platinum, or a platinum alloy such as platinum/iridium, platinum/cobalt or platinum/tungsten, and the return electrode 32 is a stainless steel tube. The return electrode 32 is completely enveloped by an polyimide insulating sheath 33. The return electrode 32 extends the entire length of the electrosurgical instrument, and constitutes the shaft of the instrument. Thus, the return electrode 32 is maintained at a relatively low temperature due to the thermal conduction therealong.

The electrodes 31 and 32 are provided with current from the radio frequency (RF) generator 1, the return electrode 32 being directly connected to the generator and the active electrode 31 being connected via a copper conductor 34. The generator may be as described in the specification of our co-pending European Patent Application No. 96304558.8. The active electrode 31 is held centrally within the return electrode 32 by means of a ceramic insulator/spacer 35. The insulator/spacer 35 has a generally cylindrical portion 35a surrounding the junction between the active electrode 31 and the conductor 34 and the adjacent regions of these two members, and four radially-extending, equispaced wings 35b which contact the internal circumferential wall of the return electrode 32 to hold the insulator/spacer, and hence the active electrode 31, centrally within the return electrode.

A tube 36, made of an insulating material such as PTFE, is a friction fit around the proximal end of the cylindrical portion 35a of the insulator/spacer 35, and extends substantially along the entire length of the instrument. The tube 36 defines, together with the return electrode 32, a coaxial saline supply channel 37, the interior of the tube 36 defining a saline return channel 38. In use, saline is fed to the channel 37 under gravity (no pumping being required), and saline is removed via the channel 38 and apertures (not shown) in the cylindrical portion 35a of the insulator/spacer 35 by means of suction. Preferably, the suction is carried out by a low noise pump (not shown) such as a moving vane pump or a diaphragm pump, rather than by using a high speed impeller. As the tubing leading to the pump will intermittently contain small quantities of saline, a large vacuum (at least 500 m Bar) is required. However, the quantity of gas and liquid to be removed is comparatively small, and this permits the use of a moving vane or diaphragm pump, although a high volume peristaltic pump could also be used.

To circumvent the requirement for pump sterilisation, the pump operates via a disposable fluid trap (not shown) incorporating a 10 .mu.m PTFE filter. This filter prevents both exhausted fluids and gas particulates from being drawn in by the pump and contaminating its workings and the surrounding environment.

The instrument described above is intended for use in open air or gas filled environments, in body fluids, or by insertion into tissue by the creation of a conductive fluid environment around the tip of the instrument, and it is so arranged that it is possible to create a local saline field at a distal end of the instrument. This instrument can, therefore, be used for laparoscopic applications. In use, saline is fed to the active electrode 31 via the channel 37, the saline providing a conductive medium to act as a conductive path between the tissue being treated and the return electrode 32. By varying the output of the generator 1, the instrument can be used for tissue removal via vaporisation, for cutting or for desiccation. In each case, as saline contacts the active electrode 31, it heats up until it reaches an equilibrium temperature dependent upon the power output of the generator 1 and the flow rate of the saline. In equilibrium, as fresh saline is fed via the channel 37 to the active electrode 31, the exterior temperature of the shaft is maintained at the same temperature as of that of the surrounding saline. As the insulating sheath 33 completely covers the external surface of the return electrode 32, accidental contact between the return electrode and tissue is avoided.

One of the advantages of using a low saline flow rate, is that the saline temperature can reach boiling point. However, as there is a continuous flow of saline, there is a temperature gradient rise in the saline from the return electrode 32 to the active electrode 31. This temperature gradient is important, as the hotter saline adjacent to the active electrode 31 reduces the power threshold requirement to reach vaporisation. Although the flow rate requirement can be calculated on the basis of the input power, the flexibility of the generator 1 in maintaining optimum power density means that the flow rate is non-critical. For example, if the generator 1 is set for 100 W, then the maximum flow rate is theoretically calculated as follows:

Flow rate

=power/specific heat capacity

=100/4.2.times.75 cc/s

=0.32 cc/s

=19 cc/min

This assumes an initial saline temperature of 25.degree. C., and a heat capacity of 4200 J/kg/.degree. C.

Although during vaporisation saline is brought into the vapour state, the vapour is only stable around the active electrode 31. Thus, the energy absorbed by virtue of the latent heat of vaporisation can be ignored, as this energy is recovered by freshly-arriving saline.

Another important factor is that, due to the very short circuit path of the saline, the current may be regarded as flowing along a number of different paths, which, therefore, do not have the same power density. Consequently, vaporisation can occur at flow rates higher than the calculated maximum, due to the unequal power densities within the saline environment. However, the amount of vaporisation occurring along the length of the active electrode 31 will depend upon the flow rate.

As the saline is heated up by the active electrode 31, it is potentially damaging to tissue as it can cause thermal necrosis. It is important, therefore, that all the heated saline is recovered and exhausted from the patient before coming into contact with the tissue adjacent to the application site. It is for this reason that there is suction from the active electrode 31 to an exhaust reservoir (not shown). However, by ensuring that the suction occurs in excess, no saline can then escape from region of the active electrode 31 other than via the saline return channel 38. Any saline which escapes transversely beyond the exterior shaft falls away from the current path, and so is not heated. The priority is, therefore, to ensure that the hottest saline is removed. As the thermal gradient is at a maximum adjacent to the active electrode 31 this is the most appropriate exhaust point for the saline. It is for this reason that the saline is exhausted through the cylindrical portion 35a of the insulator/spacer 35.

Another important consideration in deciding the point of saline evacuation is the potential for blockage of the exhaust path. This could occur when cutting or vaporising tissue in such a way as to free small tissue particles which could easily block the exhaust. The exhaust point is, therefore, selected to be at the highest energy density point on the active electrode 31. This measure ensures that any tissue approaching the exhaust point is instantly vaporised into solution, thereby avoiding the potential for blockage.

Another significant advantage of ensuring a high degree of suction during tissue removal by vaporisation, is that any smoke which has not been absorbed by the saline is also evacuated. This is important, because smoke is capable of transmitting viable biological particles, and this could lead to infection.

As mentioned above, the power threshold for vaporisation is not well defined. If the instrument were operating in a static conductive medium, then the vaporisation threshold would be well defined by an impedance switching point where the electrode impedance suddenly rises as a result of vapour pockets forming around the active electrode 31. The threshold is normally dependent upon the dissipation mechanism of the saline. In a static environment, the dissipation mechanism is predominantly by convection currents within the saline. Under these circumstances, the power threshold for vaporisation is defined by the input power into the electrode active region being in excess of the dissipation from the saline. However, in the embodiment, described above, the saline around the active electrode 31 is continually refreshed. If it were not, then the only dissipation mechanism would be by latent heat of vaporisation, and the saline would quickly evaporate. By providing a flow, the threshold power level is increased. However, the threshold power level is dependent on the saline refresh rate at the very periphery of the active electrode 31. The refresh rate at this boundary layer can be modified by altering the surface finish of the active electrode 31. For example, if the active electrode 31 had a smooth surface, then saline would be rapidly refreshed, as a rapid flow rate would be established. However, as the active electrode 31 has an irregular finish, the refresh rate of pockets within the irregular surface is diminished. Thus, the irregular surface traps saline (or at least delays the refresh) and vapour, and so absorbs more power before being replaced. In other words, the power threshold is decreased by the irregular active electrode surface. This is a highly desirable property, as the electrode power requirement drops substantially without adversely effecting tissue performance. The threshold power is further reduced because the active electrode 31 is constructed so as to provide a capillary action. Thus, even in the vaporised state, the active electrode 31 is intermittently wetted. By ensuring that this wetting wets the entire active electrode 31 by capillary action, there is a continual source of vapour which minimises the intermittent wetting, and so further reduces the power demand.

The return electrode 32 has a smooth polished surface which has no impediment to convection currents. Consequently, the return electrode 32 does have a constantly changing saline boundary layer which is replaced at a high rate, and the return electrode has a high power threshold. Moreover, the return electrode 32 forms one edge surface of the saline feed channel 37, so that there is a turbulent flow of saline along the return electrode. This results in the boundary layer replacement being very rapid, and the electrode 32 itself being cooled by the flow. The resultant increase in the power threshold of the return electrode 32 means that vaporisation can never occur at the return electrode. Indeed, the power threshold of the return electrode 32 is increased in this way so that it is considerably in excess of the maximum available power. This ensures that, even if the return electrode 32 is partially obscured, or the flow of saline impeded, the power threshold at the return electrode will never be reached. As the power threshold for vaporisation at the return electrode 32 cannot be reached, there is no risk of tissue being vaporised by the return electrode. Collateral tissue damage is, therefore, avoided. Moreover, as the saline exhaust channel 38 is inside the return electrode 32, the hottest saline is removed efficiently, thereby precluding tissue damage by plumes of heated saline leaving the active electrode 31.

By varying the output of the generator 1, the electrode unit E1 can also be used for desiccation (coagulation). In this case, the generator 1 is controlled so that small vapour bubbles form on the surface of the active electrode 31, but insufficient vapour is produced to provide a vapour bubble (pocket) surrounding the active tip of the electrode, the vapour bubble being essential for tissue removal by vaporisation.

The generator 1 is controlled in such a manner that it has respective output ranges for tissue desiccation and for tissue removal by vaporisation. The former range is from 150 volts to 200 volts, and the latter range is from 250 volts to 600 volts, the voltages being peak voltages. In the vaporisation mode, the generator 1 is controlled in such a manner as to prevent the active electrode 31 overheating. This requires a reduction in the output voltage of the generator 1 once a vapour pocket has been established. The generator 1 and its control means are described in greater detail in the specification of our European Patent Application 96304558.8

The coagulation from this electrode is vastly superior to any conventional bipolar electrode. The reasons are two fold. Firstly, the coagulation mechanism is not merely by electrical current in the tissue, but is also due to the heated saline. Secondly, under normal circumstances, the weakest link in providing electrical power to the tissue is the electrode interface, as this is the point of highest power density, and so imposes a power limit. If too high a power level is attempted, the tissue at the interface quickly desiccates, far faster than the larger cross-section of tissue forming the remaining circuit. If a lower power is selected, the interface can dissipate the temperature rise by mechanisms other than vaporisation. Consequently, the interface remains intact longer, and so a greater depth of effect can be achieved. In this embodiment, the electrical interface is much stronger by virtue of the saline, and it is not possible completely to desiccate the target tissue. Thus, power can be delivered at a higher rate and for a longer period, resulting in a depth of effect which is purely time and power related.

Vaporisation threshold control is an important aspect of such a multi-functional active electrode, the active electrode area being maximised for desiccation, whilst still being capable of vaporisation or cutting functions by retaining the vapour pocket and heated saline in the interstices of the active electrode.

As mentioned above, a fundamental feature of the design of a bipolar electrosurgical instrument is the ratio of the contact areas of the return electrode and of the active electrode. This ratio should be high for vaporisation and low for desiccation. A balance must, therefore, be struck for multi-functional electrodes. The electrode unit E1 achieves this balance by minimising the ratio to ensure efficient desiccation, and by providing vaporisation threshold control to ensure efficient vaporisation.

FIG. 4 shows the electrode assembly of the second form of electrode unit E2. This unit E2 has a shaft (not shown) for detachably fastening the unit to the electrosurgical instrument handpiece 3. The electrode assembly is positioned at the distal end of the shaft, means (not shown) being provided at the other end of the shaft for connecting the electrode assembly to the handpiece 3 both mechanically and electrically.

The electrode assembly includes a central, tissue contact (active) electrode 41 which is exposed at the extreme distal end of the instrument. The active electrode 41 is made of twisted strands of a metal such a tungsten, or a noble metal such as platinum, or a platinum alloy such as platinum cobalt, platinum/iridium or platinum/tungsten. The active electrode 41 is electrically connected to the RF generator by a central conductor (not shown). An insulating sleeve 42 surrounds the active electrode 41 and the inner conductor, the distal end of the insulating sleeve being exposed proximally of the exposed part of the electrode 41. The sleeve 42 is made of a ceramic material, silicone rubber or glass. A return electrode 43 surrounds the sleeve 41, the return electrode being in the form of a stainless steel tube. The return electrode 43 is constituted by the distal end portion of the shaft of the instrument, and is electrically connected to the RF generator. An outer insulating polyamide coating (not shown) surrounds that portion of the shaft adjacent to the return electrode 43.

The electrode unit E2 of FIG. 4 is intended for tissue removal by a vaporisation within a distension medium in the form of an electrically conductive liquid such as saline. In this case, the power threshold required to reach vaporisation is dependent on the power dissipation capability of the active electrode 41 and the flow characteristics around it. As the electrode assembly is immersed in saline, power dissipation is by electrical conversion to heat. The heated saline rises as a plume from the active electrode 41 by the action of convection. Under these circumstances, the power threshold of vaporisation is dependent on the maximum rate of convection from the active electrode.

The highest power density exists at the surface boundary of the active electrode 41. Power density falls off at a rate proportional to 1/d.sup.2 where d is the distance away from the active electrode 41. Therefore, it is the saline at the surface of the electrode 41 which defines the power threshold. The rate of saline replacement by convection and conduction losses at this point defines the power threshold. As soon as this boundary layer vaporises, then the electrode 41 becomes stable in vaporisation with a lower power level.

The irregular surface of the active electrode 41 traps saline, and so absorbs more power before being replaced. A highly polished active electrode would have a constantly changing saline boundary layer, due to the convection currents "washing" its surface. In this case, the boundary layer would be replaced at a high rate, so there would be a high power threshold. The irregular surface of the active electrode 41, however, results in the trapping of saline (and vapour) so that the saline boundary layer changes at a low rate. Thus, the irregular surface of the active electrode 41 defines a number of peaks and troughs. The saline at the boundary layer of the peaks will be replaced readily by the convection currents. However, the convection of saline in the troughs will be impeded. Thus, the saline in the troughs will not be replaced as quickly, and so will absorb more power before being replaced. In other words, the power threshold is decreased by the irregular surface of the active electrode 41. As with the embodiment of FIG. 2, this is desirable as the electrode power requirement drops substantially without adversely affecting tissue performance. The threshold power is further reduced because the active electrode 41 is constructed so as to provide a capillary action. Thus, even in a vaporised state, the active electrode 41 is intermittently wetted. By ensuring that this wetting wets the entire active electrode 41 by capillary action, there is a continual source of vapour which minimises the intermittent wetting, and so further reduces the power demand.

In the electrode unit E2 of FIG. 4, the strands are shown loosely twisted, so that adjacent strands touch each other either at spaced positions or not at all. Such a structure leaves a series of openings in the electrode that connect to a central axial cavity within the electrode structure lying along the longitudinal axis of the electrode. To prevent the electrode from fraying at its tip, the distal ends of the strands may be connected together, such as by welding or another fusing method.

Referring to FIG. 5, in a variation of the embodiment of FIG. 4, an alternative electrode unit E3 has a plurality of conductive strands which are twisted or otherwise interlaced tightly about each other, so that adjacent strands press tightly against each other, causing any cavities lying along the electrode longitudinal axis within the twisted structure to be small or non-existent. In this embodiment, substantially all the pockets for trapping conductive fluid are located at the outer surface of the electrode, in and along the joins between adjacent strands. The preferred material for the strands is an alloy of platinum or iridium. The tightly-wound configuration provides a more rigid structure than that of electrode unit E2 shown in FIG. 4. Again, the strands are welded together at the extreme distal end of the electrode.

In a further alternative electrode structure, not shown in the drawings, the central, tissue treatment (active) electrode 41 may be formed from a single length of conductive material with helical ridges formed in its outer surface, either created by moulding, machining, or by twisting a piece of the material (preferably of non-circular cross-section) about its longitudinal axis to cause spiralling ridges about the outer surface. As before, the ridges create pockets therebetween. Formation of spiralling ridges from a non-circular cross-section length of material may be performed by twisting the material so that the ridges are formed in the same way as ridges are formed when an elastic band is twisted about its own axis.

The above described alternatives to the twisted and interlaced structure of FIG. 4 may also be used in the embodiment of FIG. 3.

FIGS. 6 to 8 show modified versions E4 to E6 of the electrode units E2 and E3 of FIGS. 4 and 5, so like reference numerals will be used for like parts, and only the modifications will be described in detail. Thus, the electrode unit E4 of FIG. 6 includes an active electrode 51 in the form of a helical coil, the active electrode being made of tungsten, a noble metal such as platinum, or of a platinum alloy such as platinum/iridium, platinum/cobalt or platinum/tungsten. In use, saline is trapped between adjacent turns of the coil, so here again the saline boundary layer changes at a low rate, thereby ensuring that the active electrode 51 has a low power threshold. The active electrode 51 has the additional advantage that saline is trapped within the coil itself, thereby leading to a further reduction in the replacement rate of saline at the boundary layer, and a consequent further reduction in the power threshold.

FIG. 7 shows an electrode unit E5 having an active electrode 61 in the form of a brush constituted by a plurality of filaments made of tungsten, a noble metal such as platinum, or a platinum alloy such as platinum/iridium, platinum/cobalt or platinum/tungsten. In use, saline is trapped within the strands of the filaments, once again leading to a reduction in the replacement of saline at the boundary layer, and a reduction in the power threshold. The filaments of the brush electrode 61 also provide a capillary action, further reducing the power threshold.

The electrode unit E6 of the embodiment of FIG. 8 is similar to that of FIG. 6, having an active electrode 51 is in the form of a coil made of tungsten, a noble metal such as platinum, or a platinum alloy such as platinum/iridium, platinum/cobalt or platinum/tungsten. In this embodiment, however, the insulating sleeve 42 is formed with an arcuate extension 42a which constitutes a shroud. The inner surface of the shroud 42a closely overlies the turns of the coil electrode 51 over about half its circumference. The shroud 42a does, therefore, impede convection current flow, thereby increasing the ability of the electrode assembly to trap saline, and so leads to a further decrease in the power threshold. This electrode assembly benefits from a secondary mechanism. Thus, when in the vaporising state, tissue destruction yields gaseous products. The shroud 42a captures these gaseous products, and so excludes conduction by virtue of the insulating properties of these gaseous products.

FIG. 9 shows a further form of electrode unit E7 having an active electrode 71 in the form of a roller ball. The roller ball electrode 71 is made of stainless steel, and is rotatably supported on an arm 72 made of an electrically-conductive material such as copper. A generally hemispherical shroud 73 is fixed to the arm 72 so as to closely surround about half of the area of the ball electrode 71. The shroud 73 is made of an insulating material such as a ceramic material, silicone rubber or glass. A return electrode 74 made of stainless steel is mounted on that side of the shroud 73 remote from the ball electrode 71. Here again, the shroud 73 traps saline between its inner surface and the outer surface of the roller ball electrode 71, so the power threshold of the active electrode is reduced. The shroud 73 also traps the products of vaporisation to reduce the effective size of the large active electrode 71. Moreover, by excluding a direct return path through the saline, the return:active area ratio is effectively increased. This feature reduces the amount of power required to support vaporisation, and enables the use of a much larger active electrode 71 than would otherwise be possible. Another advantage of the shroud 73 is that it preserves the environment in the immediate region of the active electrode 71 from disturbances which otherwise would be created by the flow of saline.

FIG. 10 shows another form of electrode unit E8 having an active electrode 81 which is constituted by a needle electrode 81a made of tungsten, a noble metal such as platinum, or a platinum alloy such as platinum/iridium, platinum/cobalt or platinum/tungsten coated with a conductive ceramic material 81b. The coating 81b increases the power dissipation at the saline boundary layer, by increasing the local power density within the active electrode 81. This results in an increase in the interfacing impedance between the electrode 81 and the saline. This increase in power dissipation leads to a reduction in the power threshold of the electrode 81. This method of reducing the power threshold of an active electrode 81 is particularly useful for situations where active electrode is necessarily very small due to the limitations imposed by certain operational requirements. Obviously, the electrode 81a could be coated with any other highly resistive inert material, such as a highly resistive metal plating which is capable of withstanding the elevated temperatures associated with the vaporisation of tissue. Alternatively, the local power density of the electrode 81a could be increased by spraying it with a porous insulating material such as a ceramic material, the spraying being such as to produce spots of insulation on a conductive surface.

The return electrode of each of the embodiments of FIGS. 4 to 10 has a smooth polished surface which has no impediment to convection currents. As with the embodiment of FIG. 2, therefore, each of these return electrodes has a high power threshold for vaporisation, so that there is no risk of tissue being vaporised by the return electrode, and no risk of collateral tissue damage. The electrode assembly of each of these embodiments could be positioned adjacent to the saline supply port of an endoscope so that saline will flow over the return electrode to provide a turbulent flow of saline along that electrode. This would result in the boundary layer replacement at the return electrode being very rapid, and further increase the power threshold of the return electrode.

As mentioned above, multifunctional electrode units require vaporisation threshold control, and a minimum for the ratio of the contact areas of the return electrode and the active electrode. The minimum ratio depends on four important criteria, namely:

1. The intrinsic impedance of the target tissue;

2. The volume of the body cavity;

3. The configuration of the active electrode.

4. The maximum output power from RF generator.

The configuration of the active electrode obviously influences the ratio, with cylindrical forms representing the lowest ratio for a given length, but the other factors relate to the ability of the electrode to retain the vapour bubble. The filaments of the brush-type electrodes retain vapour bubbles, which helps maintain the vaporisation condition. As a result, the ratio for this type of electrode can be lowest of the multifunctional electrodes; and, when combined with application to tissue with high impedance, the ratio is similar to that for desiccate functions, that is in the region of 1:1 to 2:1. With solid electrode forms, however, the transition and maintenance of the vaporisation condition at similar ratios requires very high power levels (greater than 150 w at 1.5 mm diameter) for a given electrode size. As a result, the ratio must be elevated for these forms to the region of 2:1 to 3:1. Changing the exterior surface with a variety of grooves or cuts, or by using coiled wire to produce a similar form, assists vaporisation performance by stimulating the vapour pocket retention of the brush-type electrodes, thereby allowing a reduction in the ratio.

An arthroscopic electrode may be characterised as short (100-140 mm), rigid, and having a working diameter up to 4 mm. If can be introduced through a stab incision into a joint cavity (with or without a cannula) using the triangulation technique. It is operated with a motion which commonly moves the electrode between the 9 o'clock and 3 o'clock positions on the arthroscopic image. As a result, the tissue to be treated is commonly approached at a shallow working angle with respect to the axis of the electrode. The active electrode, therefore, needs to include a range of end-effect to side-effect properties. In certain circumstances, an end-effect is desirable, particularly as an end-effect is very difficult to obtaining using a shaver device wherein the centre of rotation represents the desired point of application. The tissue to be treated (such as meniscal cartilage) is commonly dense and of a high electrical impedance with a free edge of the cartilage representing the common site of injury where treatment is required. The electrode units E1, E2, E3, E4, E5 and E8 are end-effect electrode units suitable for arthroscopic use.

Either extensions or side-effect configurations of the insulator material assist with engagement, and prevent unwanted effects occurring in adjacent structures--usually the articular surfaces of the femur and tibia. In addition, the extension or side-effect electrode forms (of FIGS. 8 and 9) also assist in retaining the vapour pocket, and prevent cooling of the saline in the immediate vicinity of the active electrode by the flow of saline irrigant commonly from the endoscope.

The risk of heating distension fluid within the joint cavity occurs primarily during power application to reach the vaporisation threshold. Once the threshold has been reached, power requirements typically fall by 30-50%. Reducing the ratio increases the power requirement to reach the threshold so that, despite the high impedance of the target tissue, it is undesirable to reduce the ratio to the lowest value capable of supporting vaporisation. The feature of vaporisation threshold control retains vapour pockets and heated saline in the interstices of the electrode, and configures the insulator to reduce the effect of irrigant flow, thereby assisting in reducing the power required to establish vaporisation and hence the risk of unwanted heating.

By way of example, the coiled wire-form electrode of FIG. 6 entraps vapour products, as does the electrode of FIG. 8 (a side-effect form with the added feature of the insulator shrouding the non-contact region of the active electrode). The addition of the insulator shrouding feature can halve the power required to reach the vaporisation threshold.

Typically, in arthroscopic use, the primary function comprises rapid debulking of dense, avascular tissue. The volume of tissue removed can be increased for a given size of electrode by a combination of the vaporisation threshold control feature and by increasing the output voltage from the RF generator 1. FIG. 11 shows a schematic of the brush-type electrode of FIG. 7, wherein the vapour threshold is exceeded, and a vapour pocket, indicated by the reference P, is established around each of the filaments. When applied to tissue, particularly firm, dense tissue such as that comprising meniscal cartilage, the result will be vaporisation of a series of grooves in the tissue corresponding each of the filaments. Increasing the RF output voltage will increase the size of the vapour pockets around each of the filaments which, because of the retention will reach the stage, shown in FIG. 12, where they merge to form a contiguous vapour pocket, indicated by the reference P', so that tissue which may otherwise have passed between the filaments is also vaporised.

Our European Patent Application No. 96304558.8 discloses discrimination between desiccation and vaporisation output functions. It also discloses that a blended function can be created by constantly alternating between these output states. Vaporisation threshold control is particularly advantageous in these circumstances, as the hot saline created by the desiccate output phase is retained in proximity to the active electrode such that the vaporisation threshold is rapidly exceeded during the vaporisation cycle. This is useful as a method to achieve simultaneous desiccation when detaching muscle from bony attachments, such as is performed in an acromioplasty of the shoulder joint, or when debulking diseased tissue with a vascular component such as synovium.

The embodiment of FIG. 9 is particularly useful with a resectoscope to perform electrosurgical vaporisation of the prostate (EVAP). This particular configuration comprises a roller bar (cylindrical) active electrode 71, typically 2.4 to 3 mm in diameter by 3 to 4 mm in width. It is evident that the return electrode 74 could be mounted in an axially-separated arrangement on the shaft 72. Under these circumstances, however, the size of the active electrode 71, and the exposure of the complete surface area to the conductive environment as well as the cooling effect of irrigant flow over the electrode, would require a very high power to reach the vaporisation threshold.

It will be appreciated that the electrode 71 can be grooved or ridged so as to further reduce the vaporisation threshold. Similarly, the side-effect active electrode of FIG. 8 which could be axially or transversely mounted with respect to the axis of the resectoscope), could be substituted for the electrode assembly of FIG. 9. In this case, the active electrode would not provide a mechanical rolling function.

This instrument can also be used to perform electrosurgical vaporisation of soft tissue tumours, such as a prostatic adenoma, without use of a dispersive return plate in a conductive fluid environment. It can also be applied to fibroids using a resectoscope in the uterine cavity.

FIGS. 13 to 15 show a modified form of the electrode unit E6 of FIG. 8. This electrode unit E9 has an active electrode 91 in the form of a coiled-spring electrode mounted within a cut-out 92a.sup.1 formed in an arcuatic extension 92a of an insulation member 92, the arcuate extension forming a shroud for the active electrode. The coiled-spring electrode 91 is made of tungsten or an alloy of tungsten or platinum, and its proximal end is connected to the RF generator 1 by an insulated central copper conductor (not shown). As shown in FIG. 14, the insulation member 92 is formed with a recess 92b which receives a return electrode 93 having an extension 93a (see FIG. 15) which overlies the active electrode 91.

As shown in FIG. 15, the active electrode 91 has a distal end portion which is exposed at the distal end of the instrument for tissue contact. This embodiment has advantages over the earlier embodiments, particularly where access is needed to remote areas of a joint cavity.

FIG. 15 illustrates the way in which the insulation member 92 projects laterally in the region between the active electrode 91 and the extension 93a of the return electrode 93. This laterally-projecting part of the insulation member 92 increases the conductive fluid path length from the active electrode 91 to the return electrode 93, and forces the electric field outwardly, thereby preventing preferential arcing between the return electrode and the nearest part of the active electrode, and promoting arcing between the active electrode and the neighbouring tissue. The return electrode 93 is spaced from the active electrode 91 so that, in use, it does not contact the tissue to be treated, and so that the electrical circuit is always completed by the saline, and not simply arcing between the electrodes. Indeed, the arrangement is such that arcing between adjacent parts of the electrode assembly is avoided, thereby ensuring that the active electrode 91 can become enveloped in a vapour pocket, so that tissue entering the vapour pocket becomes the preferred path for current to flow back to the return electrode 93 via the conductive fluid.

To consider the operation of the electrode unit E9 in more detail, when it operates in a tissue cutting or vaporising mode, a vapour bubble is formed around the tip 91a of the active electrode 91. This tip 91a constitutes an active electrode treatment portion. This bubble is sustained by arcing within it. The greater the applied voltage, the greater is the size of the bubble. The energy dissipated by each arc is impedance-limited by the remaining fluid in the conduction path, and by the source impedance of the generator. However, an arc behaves as a negative impedance in that, if the energy in the arc is sufficiently high, an ionised path of very low impedance is formed. This can lead to an unstable condition of ever-decreasing ionised path impedance, unless the impedance of the fluid between the bubble and the return electrode 93 is sufficient to act as a limit on dissipated power. It is also possible for the vapour pocket around the active electrode treatment portion 91a to encroach the return electrode 93. In these circumstances, the arc energy is limited only by generator source impedance, but such power limitation is poor and cannot be adjusted according to electrode size. For these reasons, the dimensions and configuration of the insulation member 92 should be such as to define a minimum conduction path length of 1 mm between the active electrode treatment portion 91a and the fluid contact surface of the return electrode 93. This minimum path length is, in the case of the embodiment shown in FIG. 15, the arc length a of the insulation member 92 plus the step dimension c of the laterally-projecting part of the insulation member.

A further consideration is the possibility of a vapour pocket forming only over part of the exposed treatment portion 91a of the active electrode 91. When the applied voltage and power are sufficiently high a vapour pocket will form around the active electrode exposed treatment portion 91a. Preferably, the pocket is formed uniformly over the entire length of the treatment portion 91a. In such a situation, the load impedance presented to the generator 1 can change by as much as a factor of 20. However, when there are significant differences in the conduction path length between the return electrode fluid contact surface 93a and different parts of the exposed active electrode treatment portion 91a, a voltage gradient is established over the length of each electrode. With some insulation member and active electrode configurations, the voltage gradient can be sufficiently large to enable vapour pocket formation only over that part of the exposed treatment portion closest to the fluid contact surface, leaving the extreme distal end of the exposed treatment portion still in contact with the conductive fluid. Thus, the voltage gradient is established within the conductive fluid where the edge of the vapour pocket intersects the surface of the active electrode treatment portion 91a. The electrical behaviour of such a partially-enveloped active electrode treatment portion 91a is very different from that of a fully-enveloped treatment portion. In terms of controlling generator output by sensing peak voltage, the behaviour of the electrode assembly is no longer bistable. However, the power demand is considerably higher as a result of the vaporisation voltage presented across the low impedance wetted region of the active electrode treatment portion 91a. The clinical effect is not only the required vaporisation, but also a potentially undesirable thermal damaging effect resulting from the increased power dissipation.

Partial enveloping of the active electrode trode treatment portion 91a can be largely avoided by ensuring that the ratio of the length (b) of the conductive path between the furthermost point of the active electrode treatment portion and the length of the shortest conductive path between the active electrode treatment portion and the fluid contact surface is at most 2:1 i.e. b/(a+c).ltoreq.2. The laterally-projecting portion of the insulation member 92 defines an insulation barrier to direct electrical current flow through the fluid medium, thereby increasing the shortest conductive path between the fluid contact surface 93a and the active electrode 91.

It will be noted from FIG. 15, that the downward extent of the exposed active electrode treatment portion, i.e. the distance d by which the active electrode projects beyond the shrouding parts of the insulation member 92 on each side, is at least one half of the width of the exposed treatment portion in a transverse plane. This allows the instrument to be rotated about the axis of its shaft to some extend without losing the required surgical effect.

FIG. 15 also shows that the active electrode 91 has an exposed end (the tip 91a) which extends laterally through the cut-out 92a.sup.1 in a first direction which is opposite to the direction in which the fluid contact surface 93a faces. This first direction defines a treatment axis which lies in a common plane with the two shortest conductive paths referred to above.

By varying the output of the generator 1, each of the electrode units E1 to E9 can be used for tissue removal by vaporisation, or for desiccation. FIG. 16 illustrates how the RF generator 1 can be controlled to take advantage of the hysteresis which exists between the desiccation and the vaporising modes of an electrode unit. Thus, assuming the electrode assembly of the electrode unit is immersed in a conductive fluid medium such as saline, there is an initial impedance "r" at point "O", the magnitude of which is defined by the geometry of the electrode assembly and the electrical conductivity of the fluid medium, The value of "r" will change when the active electrode contacts tissue, the higher the value of "r", the greater the propensity of the electrode assembly to enter the vaporisation mode. When RF power is applied to the electrode assembly, the fluid medium heats up. Assuming the fluid medium is normal saline (0.9% w/v), the temperature coefficient of the fluid medium is positive, so that the corresponding impedance coefficient is negative. Thus, as power is applied, the impedance initially falls and continues to fall with increasing power dissipation to point "B", at which point the saline in intimate contact with the electrode assembly reaches boiling point. Small vapour bubbles form on the surface of the active electrode and the impedance then starts to rise. After point "B", as power is increased further, the positive power coefficient of impedance is dominant, so that small increases in power now bring about large increases in impedance.

As a vapour pocket forms from the vapour bubbles, there is an increase in the power density at the residual electrode/saline interface. There is, however, an exposed area of the active electrode not covered by vapour bubbles, and this further stresses the interface, producing more vapour bubbles and thus even higher power density. This is a run-away condition, with an equilibrium point only occurring once the electrode is completely enveloped in vapour. The only means of preventing the run-away condition is to limit applied voltage, thereby preventing power dissipation into higher impedance loads. For given set of variables, there is a power threshold before this new equilibrium can be reached (point "C").

The region of the graph between the points "B" and "C", therefore represents the upper limit of the desiccation mode. The transition from point "C" to the vaporise equilibrium state will follow the power impedance curve for the RF stage of the generator (shown as a dotted line in FIG. 16). Once in the vaporisation equilibrium state, the impedance rapidly increases to around 1000 ohms, with the absolute value depending on the system variables. The vapour pocket is then sustained by discharges across the vapour pocket between the active electrode and the vapour/saline interface. The majority of power dissipation occurs within this pocket, with consequent heating of the active electrode The amount of energy dissipation, and the size of the pocket, depends on the output voltage. If this is too low, the pocket will not be sustained, and if it is too high the electrode assembly will be destroyed. It should be noted that, if power were delivered at the same level as point "C", the resulting voltages would cause electrode destruction. The normal operating point for an electrode used for vaporisation is illustrated by point "D". This point is defined uniquely by the combination of the impedance power characterstic for the electrode in conjunction with the vaporise voltage limit.

The dotted line E indicates the power level above which electrode destruction is inevitable. As the power is reduced, the impedance falls until, at point "A", the vapour pocket collapses and the electrode assembly reverts to the desiccation mode. At this point, power dissipation within the vapour pocket is insufficient to sustain it, so that direct contact between the active electrode and the saline is re-established, and the impedance falls dramatically. The power density at the active electrode also falls, so that the temperature of the saline falls below boiling point. The electrode assembly is then in a stable desiccation mode.

It will be apparent that each of the electrode units E1 to E9 can be used for desiccation by operating the unit in the region of the graph between the point "O" and a point in the region between the points "B" and "C". In this case, the electrode assembly would be introduced into a selected operation site with the active electrode and the return electrode immersed in the saline. The RF generator 1 would then be activated (and cyclically controlled as described below) to supply sufficient power to the electrode assembly to maintain the saline adjacent to the active electrode at, or just below, its boiling point without creating a layer of vapour around the active tip. The electrode assembly would then be manipulated to cause heating and desiccation of the tissue in a required region adjacent to the active electrode. The electrode unit can be used for vaporisation in the region between the point "D" and the dotted line F which constitutes the level below which vaporisation cannot occur. The upper part of this curve is used for tissue removal by vaporisation. It should also be appreciated that each of the electrode units could be used for cutting tissue. In the cutting mode, the electrode unit still operates with a vapour pocket, but this pocket is much smaller than that used for vaporisation, so that there is the least amount of tissue damage commensurate with cutting. Typically, the generator 1 operates at about 270 volts peak for cutting.

The generator 1 will now be described in greater detail, this generator being such as to allow both desiccation electrosurgery substantially without unwanted cell disruption, and electrosurgical cutting or vaporisation substantially without electrode burning. Although intended primarily for operation in a conductive liquid distension medium such as saline, it has application in other electrosurgical procedures, e.g. in the presence of a gaseous distension medium, or wherever rapid load impedance changes can occur.

Referring to FIG. 17, the generator 1 comprises a radio frequency (RF) power oscillator 160 having a pair output connections 160C for coupling via output terminals 162 to the load impedance 164 represented by the electrode assembly when in use. Power is supplied to the oscillator 160 by a switched mode power supply 166.

In the preferred embodiment, the RF oscillator 160 operates at about 400 kHz, with any frequency from 300 kHz upwards into the HF range being feasible. The switched mode power supply typically operates at a frequency in the range of from 25 to 50 kHz. Coupled across the output connections 160C is a voltage threshold detector 168 having a first output 168A coupled to the switched mode power supply 166, and a second output 168A coupled to an "on" time control circuit 170. A microprocessor controller 172 coupled to the operator controls and display (shown in FIG. 2) is connected to a control input 166A of the power supply 166 for adjusting the generator output power by supply voltage variation, and to a threshold-set-input 168C of the voltage threshold detector 168 for setting peak RF output voltage limits.

In operation, the microprocessor controller 172 causes power to be applied to the switched mode power supply 166 when electrosurgical power is demanded by the surgeon operating an activation switch arrangement which may be provided on a handpiece or footswitch (see FIG. 2). A constant output voltage threshold is set via the input 168C according to control settings on the front panel of the generator (see FIG. 2). Typically, for desiccation or coagulation, the threshold is set at a desiccation threshold value between 150 volts and 200 volts. When a cutting or vaporisation output is required, the threshold is set to a value in the range of from 250 or 300 volts to 600 volts. These voltage values are peak values. Their being peak values means that, for desiccation at least, it is preferable to have an output RF waveform of low crest factor to give maximum power before the voltage is clamped at the values given. Typically a crest factor of 1.5 or less is achieved.

When the generator 1 is first activated, the status of the control input 160I of the RF oscillator 160 (which is connected to the "on" time control circuit 170) is "on", such that the power switching device which forms the oscillating element of the oscillator 160 is switched on for a maximum conduction period during each oscillation cycle. The power delivered to the load 164 depends partly on the supply voltage applied to the RF oscillator 160 from the switched mode power supply 166, and partly on the load impedance 164. If the supply voltage is sufficiently high, the temperature of the liquid medium surrounding the electrodes of the electrosurgical instrument may rise to such an extent that the liquid medium vaporises, leading to a rapid increase in load impedance and a consequent rapid increase in the applied output voltage across the terminals. This is an undesirable state of affairs if a desiccation output is required. For this reason, the voltage threshold for a desiccation output is set to cause trigger signals to be sent to the "on" time control circuit 170 and to the switched mode power supply 166 when the threshold is reached. The "on" time control circuit 170 has the effect of virtually instantaneously reducing the "on" time of the RF oscillator switching device. Simultaneously, the switched mode power supply is disabled so that the voltage supplied to oscillator 160 begins to fall.

Subsequent control of the "on" time of individual cycles of the oscillator 160 will be understood by considering the internal configuration of the "on" time control circuit which is shown in FIG. 18. The circuit comprises an RF sawtooth generator 174 (synchronised at the RF oscillation frequency by a synchronisation signal derived from the oscillator and applied to a synchronisation input 1741), and a ramp generator 176 which is reset by a reset pulse from the output 168B of the voltage threshold detector 168 (see FIG. 17) produced when the set threshold voltage is reached. This reset pulse is the trigger signal referred to above. The "on" time control circuit 170 further comprises a comparator 178 for comparing the sawtooth and ramp voltages produced by the sawtooth and ramp generators 174 and 176 to yield a square wave control signal for application to the input 1601 of the RF oscillator 160. As shown by the waveform diagrams in FIG. 18, the nature of the sawtooth and ramp waveforms is such that the mark-to-space ratio of the square wave signal applied to the oscillator 160 progressively increases after each reset pulse. As a result, after a virtually instantaneous reduction in "on" time on detection of the output voltage reaching the set voltage threshold, the "on" time of the RF oscillator 160 is progressively increased back to the original maximum value. This cycle is repeated until the supply voltage for the oscillator 160 from the power supply 166 (FIG. 17) has reduced to a level at which the oscillator can operate with the maximum conduction period without the output voltage breaching the set voltage threshold as sensed by the detector 168.

The output voltage of the generator 1 is important to the mode of operation. In fact, the output modes are defined purely by output voltage, specifically the peak output voltage. The absolute measure of output voltage is only necessary for multiple term control. However, a simple term control (i.e. using one control variable) can be used in this generator 1 in order to confine the output voltage to predetermined limit voltages. Thus, the voltage threshold detector 168 shown in FIG. 17 compares the RF peak output voltage with a preset DC threshold level, and has a sufficiently fast response time to produce a reset pulse for the "on" time control circuit 170 within one RF half cycle.

Before considering the operation of the generator 1 further, it is appropriate to refer back to the impedance power characteristic of FIG. 16. It will be appreciated that the most critical control threshold is that applicable during desiccation. Since vapour bubbles forming at the active electrode are non-conducting, the saline remaining in contact with the electrode has a higher power density and consequently an even greater propensity to form vapour. This degree of instability brings about a transition to a vaporisation mode with the same power level due to the runaway increase in power density at the active electrode. As a result, the impedance local to the active electrode rises Maximum absorbed power coincides with the electrode condition existing immediately before formation of vapour bubbles, since this coincides with maximum power dissipation and the greatest wetted electrode area. It is, therefore, desirable that the electrode remains in is wetted state for the maximum desiccation power. Use of voltage limit detection brings about a power reduction, which allows the vapour bubbles to collapse which, in turn, increases the ability of the active electrode to absorb power. For this reason, the generator 1 includes a control loop having a large overshoot, in that the feedback stimulus of the peak voltage reaching the predefined threshold causes a large instantaneous reduction in power. This control overshoot ensures a return to the required wetted state.

In the generator 1 described above with reference to FIGS. 17 and 18, power reduction in response to voltage threshold detection takes place in two ways:

(a) an instantaneous reduction in RF energy supplied to the resonant output circuit of the oscillator 160, and

(b) a shut down of DC power to the oscillator 160 for one or more complete cycles of the switched mode power supply (i.e. typically for a minimum period of 20 to 40 .mu.s).

In the preferred embodiment, the instantaneous power reduction is by at least three quarters of available power (or at least half voltage) from the DC power supply, but continuous voltage threshold feedback continually causes a reduction in delivered power from the DC power supply. Thus, a high speed response is obtained in the RF stage itself, with the DC supply voltage tracking the reduction to enable the RF stage to return to a full duty cycle or mark-to-space ratio, thereby enabling further rapid power reductions when the voltage threshold is again breached.

The effect of this process on the RF output voltage is shown in the waveform diagram of FIG. 19, containing traces representative of the output voltage, the oscillator supply voltage, and the load impedance during a typical desiccation episode over a 1 ms period.

Starting on the lefthand side of the diagram with the supply voltage approximately constant, the output voltage increases with increasing load impedance to a point at which the output voltage threshold is reached, whereupon the above-described instantaneous reduction in oscillator "on" time occurs. This produces a rapid decrease in the RF output voltage, as shown, followed by a progressive increase, again as described above. When the output voltage reaches the threshold voltage, the voltage threshold detector 168 (shown in FIG. 17) also disables the power supply, leading to a gradual decrease in the supply voltage. As a result, when the "on" time of the oscillator device has once again reached its maximum value, illustrated by point a in FIG. 19, the threshold voltage has not been reached. However, the load impedance begins rising again, cause a further, albeit slower, increase in the output voltage until, once again, the threshold voltage is reached (point b). Once more, the "on" time of the oscillator is instantly reduced and then progressively increased, so that the output voltage waveform repeats its previous pattern. Yet again, the threshold voltage is reached, again the output voltage is instantly reduced (at point c), and again the "on" time is allowed to increase. On this occasion, however, due to the supply voltage having further reduced (the power supply still being disabled), the output voltage does not reach the threshold level (at point d) until a considerably longer time period has elapsed. Indeed, the length of the period is such that the output voltage has failed to reach the threshold voltage over a complete switching cycle of the power supply, so that it has in the meantime been enabled (at point e).

The generator output impedance is set to about 160 ohms. The effect of this choice will be evident from the following description with reference to FIGS. 20 and 21 which are graphs showing the variation of output power which can be produced by the generator into different load impedances.

Referring to FIG. 20, the power delivered to the load is here shown as a function of load impedance for two different oscillator supply voltage settings. In both cases, it will be seen that, to the left of the power/impedance peak, an increase in load impedance leads to an increase in output power and, hence, an increase in output voltage. At higher impedances, to the right of the peaks, the voltage continues to increase, albeit less aggressively, as impedance increases.

One of the features of the preferred generator in accordance with the invention is that the output stage operates as an open loop oscillator with an output impedance (corresponding to the peaks in FIG. 20) of about 160 ohms. This is considerably lower than the output impedance of conventional generators used for underwater electrosurgery, and contributes to the ability to prevent runaway arcing behaviour and consequent excessive tissue damage and electrode burn-out.

It should be understood that, for desiccation, steam envelope generation to the electrode and arcing should be prevented. Conversely, for cutting or vaporisation, steam envelope generation and arcing are required, but to a level consistent with achieving the required tissue effect and the avoidance of electrode burn-out. Operating points for low and high power desiccation and cutting or vaporisation are shown in FIG. 20.

A feature of the combination of the generator in accordance with the invention and an electrode assembly having two adjacent electrodes is that the output is virtually bistable. When operating in desiccation mode, to he entire electrode surface is in contact with an electrically-conductive medium and, therefore, the load impedance is comparatively low, consequently inhibiting the rise in output voltage to a level sufficient for arcing. Conversely, when in cutting or tissue vaporisation mode, the entire active electrode surface is covered with a layer of vapour which is of much higher impedance, and the vapour pocket is sustained by arcing within it so that nearly all of the power dissipation occurs within the vapour envelope. In order to traverse from a desiccation mode to the cutting mode, a high power burst is required, hence the positioning of the power/load curve peak between the desiccation and cutting operation points on the curve. By allowing the output power to increase with impedance in this way, a high power burst of sufficient energy to create acing is achieved despite the lower impedance presented by the electrodes. As the supply voltage to the oscillator is increased, it has a greater propensity to flip into the cut mode, whilst, at lower supply voltage levels, the bistable nature of the output, although more pronounced, tends towards the desiccation state.

The bistable properties arise not only from the electrode impedance behaviour, but also from the shape of the power/load impedance curve. The flatter the load curve, the more constant the output power across a band of impedances, and the less pronounced the effect.

Referring to FIG. 20, it will be appreciated that, in the cut or tissue vaporisation mode, a power equilibrium point is achieved by virtue of the decreasing output power as impedance increases. In the desiccation mode, the equilibrium is less straightforward, because there are two impedance change mechanisms. The first mechanism is the heating of the conductive medium and/or tissue which, due its positive coefficient of conductivity, results in a fall impedance initially, so that, when power is first applied, the operating point moves towards the lefthand side of the diagram in FIG. 20. Consequently, there is a well-defined equilibrium point defined by the reduction in impedance with increasing power supply voltage, and the consequent reduction in delivered output power. However, when the saline medium or tissue fluids in contact with the active electrode start to boil, small water vapour bubbles begin to form which increase the impedance. When the generator 1 is about to flip into the cutting mode, impedance rise due to steam formation is dominant. The impedance change, therefore, becomes positive with increasing supply voltage, and the operating point moves towards the righthand side of the diagram, which allows greater input power as a result of the shape of the load curve, causing a rapid change to cutting or vaporisation mode. As steam formation continues to increase, the increasing impedance causes a fall-off in delivered output power.

The applicants have found that the inherent equilibria described above may be insufficient to maintain a stable coagulation (or desiccation) state or a stable cutting (or vaporisation) state. It is for this reason, that the RF output voltage from the RF oscillator 160 (FIG. 17) is limited, the limiting occurring extremely rapidly, typically with a response time of 20 .mu.s or less. Excessive RF interference is avoided by linear variation of the oscillator switching device "on" time in response to a feedback signal from the voltage threshold detector. This technique is used in conjunction with the RF oscillator having a comparatively low output Q when matched to the load, this Q being sufficient to suppress switching noise without inordinately damping the response to output threshold detection.

By way of example, the effect of voltage threshold control for a particular electrode configuration is shown in FIG. 21. The heavy lines 200, 202 indicate the modified power/load impedance characteristics. For desiccation, shown by line 200, the switched mode power supply is set to produce a peak (matched) open loop output power of between 75 watts and 100 watts, with the actual peak power in this case being about 90 watts. For cutting and vaporisation (shown by line 202), the peak power can be between 120 watts and 175 watts. In this case it is 150 watts. As examples, the voltage thresholds are set at 180 volts peak for desiccation and 300 volts peak for cutting, as illustrated by the hyperbolic constant voltage lines 204 and 206 respectively. The power/impedance curves follow the respective constant voltage threshold lines to the right of their intersection with the unmodified open loop curves 208 and 210. Thus, it will be understood that the desiccation threshold line represents the maximum voltage that can be achieved in the desiccation mode before arcing is produced, whilst the cut threshold line limits the cutting or tissue vaporisation performance to achieve the desired tissue effect and, in the extreme, to avoid electrode burn-out. The desiccation threshold line also represents a voltage insufficient to achieve arcing for cutting or vaporising tissue.

A significant feature of the generator characteristic for electrosurgical cutting or tissue vaporisation is that, at peak power (matched impedance), the load impedance lies between the impedances corresponding to the threshold voltages at that power level. In contrast, in the desiccation mode, the power/load impedance characteristic has a power peak at an impedance lying below the desiccation threshold line at that power level.

In practice, the output power in the desiccation mode will be higher than in the cutting or tissue vaporisation mode. The reason for this statement (despite the apparent contradiction with the load curves in FIG. 21) is that the equilibrium points described above above lie at different points on the respective curves. To ensure cutting, the high peak power of the higher curve is required to reach the cut threshold line (corresponding to 300 volts peak). The cutting mode then follows the cutting or vaporisation threshold line. The cutting operating point is defined by the load impedance created when a suitable level of arcing is occurring. Typically, the load impedance in these circumstances is greater than 1000 ohms. Thus, although a full 150 watt peak power is available to ensure that vapour pockets are formed to promote arcing for cutting, the actual power drawn during cutting or tissue vaporisation for this particular electrode example may be between 30 watts and 40 watts. This situation is more easily understood if reference is also made to FIG. 16.

In the desiccation mode, the operating point is determined by the positive power coefficient of impedance arising from steam generation. Consequently, the equilibrium naturally occurs in the region of the peak of the desiccation mode power/load impedance curve.

The electrode unit E9 of FIGS. 13 to 15 has an active electrode 91 having a fluid-contacting surface area that is 1.1 times the fluid-contacting surface area of the return electrode 93. Known bipolar instruments cannot vaporise a surrounding electrically-conductive fluid such as saline if the ratio of these areas approaches 0.5 to 1. The electrode unit E9 can, however, vaporise surrounding saline. This is because of special properties of the active electrode 91 and the generator 1, to be described below.

The active electrode of known instruments is such that the vapour pocket is established as an equilibrium between vapour creation and vapour condensation. However, in order to reach this condition, the active electrode itself must have a temperature in excess of 100.degree. C. Thermal conduction away from the active electrode before the pocket is created will, therefore, increase the power demand. It is important to realise that this thermal conduction may be along the active electrode itself, or to an adjacent component such as an insulator. During use, the active electrode may be intermittently wetted. This wetting is random, and does not necessarily wet the ensure surface of the active electrode. If a large area active electrode were constructed of thermally-conductive material, this occasional wetting could reduce the overall temperature of the active electrode so that vaporisation collapses or is quenched. Thermal conduction away from the active electrode can, however, be the only thermal dissipation mechanism for the active electrode, and so can be important. For optimum vaporisation performance, the active electrode, needs to be between the lower limit of 100.degree. C. and the destructive limit defined by its melting point.

The active electrode 91 of the electrode unit E9, though made of a material that is normally considered to be a good thermal conductor, actually has poor thermal conductivity across its surface because of the inbuilt thermal barriers constituted by the air gaps formed between the adjacent turns of the coil. The poor thermal conductivity across its surface prevents the thermal dissipation referred to above, and ensures that this unit E9 can be used in the vaporisation mode.

The other factor ensuring that the vaporisation mode can be maintained is that, as described above with reference to FIGS. 17 to 21, the generator 1 has a low source impedance of 160 ohms, and is capable of rapid voltage-dependent power reduction upon formation of a vapour pocket around the active electrode 91, thus permitting the control of high-rate vaporisation of tissue.

The electrosurgical instruments described above also have irrigated electrode applications. Thus, each utilises a method of creating a localised saline working environment as a means of completing the electrical circuit of axially separated active and return electrodes to perform tissue vaporisation, cutting and desiccation in a gas or air filled body cavity whether of natural origin or created surgically, or at a tissue surface of the body whether of natural origin or created surgically.

More specifically, each such instrument utilises a method of removing tissue by vaporisation wherein the products of vaporisation are aspirated from the site of application by suction through, or adjacent to, the active electrode assembly. Diseased tissue can be also removed by vaporisation from natural body cavities such as sinuses, nasal cavities and the oropharynx. Similarly, diseased tissue can be removed by vaporisation from the abdominal cavity under gaseous distension.

Such an instrument can also be used to create the surgical access to an interstitial site where the tissue to be treated is lying deep to the tissue surface.

It will be apparent that the invention permits power consumption during vaporisation of the conductive liquid to be reduced by hindering the dissipation of heat from the active electrode to the surroundings (particularly to the body of the instrument shaft and to the surrounding saline), so as to lower the power threshold of vaporisation. This can be achieved by limiting convection by hindering the flow of saline around the electrode, by providing recesses or spaces in and around the electrode to trap vapour, and by limiting cross-electrode thermal conduction by, for instance, forming the electrode in parts with thermal barriers between them. This latter measure reduces the possibility of vapour pocket collapse by part of the electrode being wetted and heat then being conducted away from other parts of the electrode to the wetted part.

Claims

What is claimed is:

1. An electrosurgical system for the vaporisation of tissue in the presence of an electrically-conductive medium, the system comprising an electrosurgical generator for generating radio frequency power, and an electrosurgical instrument connectible to the generator, wherein: the generator has a radio frequency output stage for delivering radio frequency power to a pair of output connections, which output stage has an open loop output impedance of less than 250 ohms; the electrosurgical instrument comprises an instrument shaft and, situated at a distal end of the shaft, an electrode assembly comprising an active electrode with an exposed treatment portion and a return electrode with an exposed fluid contact surface, the fluid contact surface being set back from the treatment portion so that, when the electrode assembly is brought into an operative position with the treatment portion on or adjacent to the surface of the tissue to be treated, the fluid contact surface is further from the tissue surface than the treatment portion; and the ratio of the surface area of the exposed treatment portion to the surface area of the exposed fluid contact surface is greater than or equal to 0.5 to 1; the electrode assembly further comprising means associated with the active electrode for hindering the dissipation of heat from the active electrode to its surroundings, thereby to encourage the formation and maintenance of a layer of vapour over its surface.

2. A system according to claim 1, wherein the heat dissipation hindering means comprises a shroud partly covering the active electrode, with a space between the shroud and the electrode to allow the ingress of the conductive liquid therebetween.

3. A system according to claim 1, wherein the heat dissipation hindering means comprises a cavity in the active electrode, which cavity is open to the ingress of the conductive liquid thereby to trap vapour from the conductive liquid.

4. A system according to claim 3, wherein the active electrode is found as a tube with at least one open end.

5. A system according to claim 4, wherein the active electrode is in the form of a tubular wire coil.

6. A system according to claim 1, wherein the active electrode is formed as a plurality of electrically-interconnected electrode parts, and the heat dissipation hindering means comprises a thermal barrier between said electrode parts to hinder heat conduction between said parts.

7. A system according to claim 6, wherein the active electrode is in the form of a tubular wire helix.

8. A system according to claim 6, wherein the active electrode comprises a metallic body with a ridged, outwardly-directed treatment surface.

9. A system according to claim 1, wherein the active electrode comprises a metallic body with an outwardly-directed irregular surface defining recesses for trapping vaporised conductive liquid.

10. A system according to claim 9, wherein the active electrode comprises a metallic body with a ridged outwardly-directed treatment surface.

11. A system according to claim 10, wherein the active electrode comprises a plurality of electrically common wire parts arranged side-by-side to form said ridged treatment surface.

12. A system according to claim 10, wherein the active electrode is in the form of a wire coil.

13. A system according to claim 1, wherein the generator includes means for limiting the peak radio frequency output voltage at said output connections to a threshold voltage in the range of from 250v to 600v peak.

14. A system according to claim 13, wherein the output range includes a radio frequency power switching device which is arranged to switch on and off repeatedly at the radio frequency of the radio-frequency output signal of the generator, and the voltage limiting means comprises a peak voltage sensor and a feedback circuit connected to the sensor and to the switching device and arranged to reduce the conductive periods of the switching device when the peak output voltage reaches said threshold.

15. A system according to claim 14, wherein the sensor and the feedback circuit are operatable in conjunction to reduce the radio frequency power delivered from the switching device to the output connections by at least 50% in less than 100 .mu.s in response to the voltage across said output connections reaching said threshold.

16. A system according to claim 1, wherein said output impedance is in the range of from 50 ohms to 250 ohms.

17. A system according to claim 16, wherein said output impedance is in the range of from 130 ohms to 190 ohms.

18. A system according to claim 17, wherein said output impedance is 160 ohms.

19. An electrosurgical instrument for the treatment of tissue in the presence of an electrically-conductive fluid medium, the instrument comprising an instrument shaft and an electrode assembly at a distal end of the shaft, wherein the electrode assembly comprises: a single active electrode having an exposed tissue treatment portion; a return electrode having an exposed fluid contact surface; and an insulating member positioned between and electrically insulating the active electrode and the return electrode, and serving to space apart the exposed treatment portion of the active electrode and the exposed fluid contact surface of the return electrode, the fluid contact surface of the return electrode being set back in the direction of a treatment axis of the assembly from the active electrode exposed treatment portion; and wherein the ratio of the area of the exposed treatment portion to the area of the exposed fluid contact surface is greater than or equal to 0.5 to 1; and the active electrode is constituted by a singled coiled filament which defines a generally tubular member, adjacent turns of the coiled filament defining indentations in said generally tubular member, said indentations constituting thermal barriers for limiting thermal conduction along said generally tubular member, whereby, in use, application of sufficient radio frequency power to the electrode assembly vaporises the conductive fluid medium adjacent to the tissue treatment portion to create a stable vapour pocket around the tissue treatment portion.

20. An electrosurgical instrument for the treatment of tissue in the presence of an electrically-conductive fluid medium, the instrument comprising an instrument shaft and an electrode assembly at a distal end of the shaft, wherein the electrode assembly comprises: a single active electrode having an exposed tissue treatment portion; a return electrode having an exposed fluid contact surface; and an insulating member positioned between and electrically insulating the active electrode and the return electrode, and serving to space apart the exposed treatment portion of the active electrode and the exposed fluid contact surface of the return electrode, the fluid contact surface of the return electrode being set back in the direction of a treatment axis of the assembly from the active electrode exposed treatment portion; and wherein the ratio of the area of the exposed treatment portion, to the area of the exposed fluid contact surface is greater than or equal to 0.5 to 1; and the active electrode is configured to define thermal barriers for limiting thermal conduction therealong, whereby, in use, application of sufficient radio frequency power to the electrode assembly vaporises the conductive fluid medium adjacent to the tissue treatment portion to create a stable vapour pocket around the tissue treatment portion.

Patent Citations (520)

Patent	Date	Inventor
USRe33925	1992-05-01	Bales et al.
US164184	1875-06-01	Kidder
US1366756	1921-01-01	Wappler
US1735271	1929-11-01	Groff
US1814791	1931-07-01	Ende
US1889609	1932-11-01	Mutscheller
US1932258	1933-10-01	Wappler
US1943543	1934-01-01	McFadden
US1952617	1934-03-01	Wappler
US1983669	1934-12-01	Kimble
US2050904	1936-08-01	Trice
US2056377	1936-10-01	Wappler
US2196171	1940-04-01	Arnesen
US2888928	1959-06-01	Seiger
US3035580	1962-05-01	Guiorguiev
US3460539	1969-08-01	Anhalt, Sr.
US3595239	1971-07-01	Petersen
US3601126	1971-08-01	Estes
US3614414	1971-10-01	Gores
US3649001	1972-03-01	Anderson et al.
US3685518	1972-08-01	Beurle et al.
US3699967	1972-10-01	Anderson
US3707149	1972-12-01	Hao et al.
US3801766	1974-04-01	Morrison, Jr.
US3815604	1974-06-01	O'Malley et al.
US3845771	1974-11-01	Vise
US3847153	1974-11-01	Weissman
US3870047	1975-03-01	Gonser
US3885569	1975-05-01	Judson
US3898991	1975-08-01	Ikuno et al.
US3901242	1975-08-01	Storz
US3902494	1975-09-01	Haberlen et al.
US3903891	1975-09-01	Brayshaw
US3920021	1975-11-01	Hiltebrandt
US3920022	1975-11-01	Pastor
US3923063	1975-12-01	Andrews et al.
US3929137	1975-12-01	Gonser et al.
US3939839	1976-02-01	Curtiss
US3945375	1976-03-01	Banko
US3963030	1976-06-01	Newton
US3964487	1976-06-01	Judson
US3970088	1976-07-01	Morrison
US3974833	1976-08-01	Durden, III
US4011872	1977-03-01	Komiya
US4016881	1977-04-01	Rioux et al.
US4024467	1977-05-01	Andrews et al.
US4033351	1977-07-01	Hetzel
US4040426	1977-08-01	Morrison, Jr.
US4043342	1977-08-01	Morrison, Jr.
US4051855	1977-10-01	Schneiderman
US4060088	1977-11-01	Morrison, Jr. et al.
US4069827	1978-01-01	Dominy
US4074718	1978-02-01	Morrison, Jr.
US4092986	1978-06-01	Schneiderman
US4114623	1978-09-01	Meinke et al.
US4116198	1978-09-01	Roos
US4119102	1978-10-01	LeVeen
US4126137	1978-11-01	Archibald
US4154240	1979-05-01	Ikuno et al.
US4189685	1980-02-01	Doss
US4200104	1980-04-01	Harris
US4202337	1980-05-01	Hren et al.
US4204549	1980-05-01	Paglione
US4210152	1980-07-01	Berry
US4228800	1980-10-01	Degler, Jr. et al.
US4248231	1981-02-01	Herczog et al.
US4271837	1981-06-01	Schuler
US4281373	1981-07-01	Mabille
US4301802	1981-11-01	Poler
US4326529	1982-04-01	Doss et al.
US4346332	1982-08-01	Walden
US4376263	1983-03-01	Pittroff et al.
US4381007	1983-04-01	Doss
US4416277	1983-11-01	Newton et al.
US4418692	1983-12-01	Guay
US4429698	1984-02-01	Bentall
US4448198	1984-05-01	Turner
US4474179	1984-10-01	Koch
US4476862	1984-10-01	Pao
US4492231	1985-01-01	Auth
US4494541	1985-01-01	Archibald
US4512338	1985-04-01	Balko et al.
US4517976	1985-05-01	Murakoshi et al.
US4524770	1985-06-01	Orandi
US4532924	1985-08-01	Auth et al.
US4534347	1985-08-01	Taylor
US4548207	1985-10-01	Reimels
US4559943	1985-12-01	Bowers
US4559951	1985-12-01	Dahl et al.
US4562838	1986-01-01	Walker
US4565200	1986-01-01	Cosman
US4567890	1986-02-01	Ohta et al.
US4580557	1986-04-01	Hertzmann
US4590934	1986-05-01	Malis et al.
US4593691	1986-06-01	Lindstrom et al.
US4617927	1986-10-01	Manes
US4657015	1987-04-01	Irnich
US4658819	1987-04-01	Harris et al.
US4658820	1987-04-01	Klicek
US4669468	1987-06-01	Cartmell et al.
US4674499	1987-06-01	Pao
US4681122	1987-07-01	Winters et al.
US4682596	1987-07-01	Bales et al.
US4688569	1987-08-01	Rabinowitz
US4696668	1987-09-01	Wilcox
US4706667	1987-11-01	Roos
US4709698	1987-12-01	Johnston et al.
US4712544	1987-12-01	Ensslin
US4727874	1988-03-01	Bowers et al.
US4735201	1988-04-01	O'Reilly
US4769005	1988-09-01	Ginsburg et al.
US4781175	1988-11-01	McGreevy et al.
US4799480	1989-01-01	Abraham et al.
US4800899	1989-01-01	Elliott
US4802476	1989-02-01	Noerenberg et al.
US4805616	1989-02-01	Pao
US4813429	1989-03-01	Eshel et al.
US4820298	1989-04-01	Leveen et al.
US4823791	1989-04-01	D'Amelio et al.
US4827927	1989-05-01	Newton
US4832048	1989-05-01	Cohen
US4850353	1989-07-01	Stasz et al.
US4860744	1989-08-01	Johnson et al.
US4878493	1989-11-01	Pasternak et al.
US4886074	1989-12-01	Bisping
US4919129	1990-04-01	Weber, Jr. et al.
US4920978	1990-05-01	Colvin
US4931047	1990-06-01	Broadwin et al.
US4936281	1990-06-01	Stasz
US4936301	1990-06-01	Rexroth et al.
US4936310	1990-06-01	Engstrom et al.
US4936842	1990-06-01	D'Amelio et al.
US4943290	1990-07-01	Rexroth et al.
US4950267	1990-08-01	Ishihara et al.
US4955377	1990-09-01	Lennox et al.
US4966597	1990-10-01	Cosman
US4967765	1990-11-01	Turner et al.
US4969885	1990-11-01	Farin
US4976711	1990-12-01	Parins et al.
US4994069	1991-02-01	Ritchart et al.
US4998933	1991-03-01	Eggers et al.
US5007908	1991-04-01	Rydell
US5009656	1991-04-01	Reimels
US5013312	1991-05-01	Parins et al.
US5019076	1991-05-01	Yamanashi et al.
US5035696	1991-07-01	Rydell
US5037379	1991-08-01	Clayman et al.
US5047026	1991-09-01	Rydell
US5047027	1991-09-01	Rydell
US5057107	1991-10-01	Parins et al.
US5062031	1991-10-01	Flachenecker et al.
US5071418	1991-12-01	Rosenbaum
US5080660	1992-01-01	Buelna
US5083565	1992-01-01	Parins
US5085659	1992-02-01	Rydell
US5088997	1992-02-01	Delahuerga et al.
US5098431	1992-03-01	Rydell
US5099840	1992-03-01	Goble et al.
US5108391	1992-04-01	Flachenecker et al.
US5108407	1992-04-01	Geremia et al.
US5117978	1992-06-01	Blumenfeld et al.
US5122138	1992-06-01	Manwaring
US5133365	1992-07-01	Heil, Jr. et al.
US5158561	1992-10-01	Rydell et al.
US5167658	1992-12-01	Ensslin
US5167659	1992-12-01	Ohtomo et al.
US5171255	1992-12-01	Rydell
US5171311	1992-12-01	Rydell et al.
US5178620	1993-01-01	Eggers et al.
US5190517	1993-03-01	Zieve et al.
US5195959	1993-03-01	Smith
US5196007	1993-03-01	Ellman et al.
US5197963	1993-03-01	Parins
US5201743	1993-04-01	Haber et al.
US5207675	1993-05-01	Canady
US5211625	1993-05-01	Sakurai et al.
US5217457	1993-06-01	Delahuerga et al.
US5217458	1993-06-01	Parins
US5217459	1993-06-01	Kamerling
US5221281	1993-06-01	Klicek
US5244462	1993-09-01	Delahuerga et al.
US5249585	1993-10-01	Turner et al.
US5250047	1993-10-01	Rydell
US5257990	1993-11-01	Nash
US5258006	1993-11-01	Rydell et al.
US5259395	1993-11-01	Li
US5261906	1993-11-01	Pennino et al.
US5267994	1993-12-01	Gentelia et al.
US5267997	1993-12-01	Farin et al.
US5277201	1994-01-01	Stern
US5277696	1994-01-01	Hagen
US5281213	1994-01-01	Milder et al.
US5281216	1994-01-01	Klicek
US5282799	1994-02-01	Rydell
US5282845	1994-02-01	Bush et al.
US5290282	1994-03-01	Casscells
US5290283	1994-03-01	Suda
US5300068	1994-04-01	Rosar et al.
US5300069	1994-04-01	Hunsberger et al.
US5300070	1994-04-01	Gentelia et al.
US5304214	1994-04-01	DeFord et al.
US5306238	1994-04-01	Fleenor
US5317155	1994-05-01	King
US5318563	1994-06-01	Malis et al.
US5320627	1994-06-01	Sorensen et al.
US5330470	1994-07-01	Hagen
US5330471	1994-07-01	Eggers
US5334193	1994-08-01	Nardella
US5334198	1994-08-01	Hart et al.
US5336222	1994-08-01	Durgin, Jr. et al.
US5342357	1994-08-01	Nardella
US5342391	1994-08-01	Foshee et al.
US5344428	1994-09-01	Griffiths
US5352222	1994-10-01	Rydell
US5354296	1994-10-01	Turkel
US5366443	1994-11-01	Eggers et al.
US5370645	1994-12-01	Klicek et al.
US5370675	1994-12-01	Edwards et al.
US5372596	1994-12-01	Klicek et al.
US5382247	1995-01-01	Cimino et al.
US5383874	1995-01-01	Jackson et al.
US5383876	1995-01-01	Nardella
US5383917	1995-01-01	Desai et al.
US5383923	1995-01-01	Webster, Jr.
US5395363	1995-03-01	Billings et al.
US5395368	1995-03-01	Ellman et al.
US5403311	1995-04-01	Abele et al.
US5419767	1995-05-01	Eggers et al.
US5422567	1995-06-01	Matsunaga
US5423808	1995-06-01	Edwards et al.
US5423809	1995-06-01	Klicek
US5423810	1995-06-01	Goble et al.
US5423811	1995-06-01	Imran et al.
US5431649	1995-07-01	Mulier et al.
US5437662	1995-08-01	Nardella
US5438302	1995-08-01	Goble
US5441499	1995-08-01	Fritzsch
US5443470	1995-08-01	Stern et al.
US5454809	1995-10-01	Janssen
US5462521	1995-10-01	Brucker et al.
US5472441	1995-12-01	Edwards et al.
US5472443	1995-12-01	Cordis et al.
US5480397	1996-01-01	Eggers et al.
US5480398	1996-01-01	Eggers et al.
US5496312	1996-03-01	Klicek
US5496314	1996-03-01	Eggers
US5505728	1996-04-01	Ellman et al.
US5505730	1996-04-01	Edwards
US5507743	1996-04-01	Edwards et al.
US5514129	1996-05-01	Smith
US5514130	1996-05-01	Baker
US5514131	1996-05-01	Edwards et al.
US5520684	1996-05-01	Imran
US5520685	1996-05-01	Wojciechowicz
US5522815	1996-06-01	Durgin, Jr. et al.
US5527331	1996-06-01	Kresch et al.
US5531744	1996-07-01	Nardella et al.
US5536267	1996-07-01	Edwards et al.
US5540680	1996-07-01	Guglielmi et al.
US5540681	1996-07-01	Strul et al.
US5540682	1996-07-01	Gardner et al.
US5540683	1996-07-01	Ichikawa et al.
US5540684	1996-07-01	Hassler, Jr.
US5540685	1996-07-01	Parins et al.
US5542916	1996-08-01	Hirsch et al.
US5542945	1996-08-01	Fritzsch
US5545161	1996-08-01	Imran
US5545193	1996-08-01	Fleischman et al.
US5549605	1996-08-01	Hahnen
US5554172	1996-09-01	Horner et al.
US5555618	1996-09-01	Winkler
US5556396	1996-09-01	Cohen et al.
US5556397	1996-09-01	Long et al.
US5558671	1996-09-01	Yates
US5562720	1996-10-01	Stern et al.
US5569164	1996-10-01	Lurz
US5569242	1996-10-01	Lax et al.
US5569244	1996-10-01	Hahnen
US5569245	1996-10-01	Guglielmi et al.
US5571100	1996-11-01	Goble et al.
US5575789	1996-11-01	Bell et al.
US5578007	1996-11-01	Imran
US5582609	1996-12-01	Swanson et al.
US5582610	1996-12-01	Grossi et al.
US5584830	1996-12-01	Ladd et al.
US5591141	1997-01-01	Nettekoven
US5599344	1997-02-01	Paterson
US5599345	1997-02-01	Edwards et al.
US5599346	1997-02-01	Edwards et al.
US5599347	1997-02-01	Hart et al.
US5599348	1997-02-01	Gentelia et al.
US5599349	1997-02-01	D'Amelio
US5603711	1997-02-01	Parins et al.
US5603712	1997-02-01	Koranda et al.
US5607422	1997-03-01	Smeets et al.
US5609151	1997-03-01	Mulier et al.
US5609573	1997-03-01	Sandock
US5611798	1997-03-01	Eggers
US5620481	1997-04-01	Desai et al.
US5624439	1997-04-01	Edwards et al.
US5626560	1997-05-01	Soring
US5626575	1997-05-01	Crenner
US5626576	1997-05-01	Janssen
US5626578	1997-05-01	Tihon
US5628745	1997-05-01	Bek
US5628771	1997-05-01	Mizukawa et al.
US5630426	1997-05-01	Eggers et al.
US5633578	1997-05-01	Eggers et al.
US5634924	1997-06-01	Turkel et al.
US5647869	1997-07-01	Goble et al.
US5672174	1997-09-01	Gough et al.
US5683366	1997-11-01	Eggers et al.
US5693045	1997-12-01	Eggers
US5697281	1997-12-01	Eggers et al.
US5697536	1997-12-01	Eggers et al.
US5697882	1997-12-01	Eggers et al.
US5697909	1997-12-01	Eggers et al.
US5700262	1997-12-01	Acosta et al.
US5725524	1998-03-01	Mulier et al.
US5766153	1998-06-01	Eggers et al.
US5810764	1998-09-01	Eggers et al.
US5833689	1998-11-01	Long
US5843019	1998-12-01	Eggers et al.
US5860951	1999-01-01	Eggers et al.
US5871469	1999-02-01	Eggers et al.
US5873855	1999-02-01	Eggers et al.
US5888198	1999-03-01	Eggers et al.
US5891095	1999-04-01	Eggers et al.
US5902272	1999-05-01	Eggers et al.
EPX13605	1980-07-01
EPX49633	1982-04-01
EPX67680	1982-12-01
EPX136885	1985-04-01
EPX219568	1985-12-01
EPX205851	1986-12-01
EPX280798A	1988-09-01
EPX310431	1989-04-01
EPX316469	1989-05-01
EPX325456	1989-07-01
EPX332308	1989-09-01
EPX373670	1990-06-01
EPX392837	1990-10-01
EPX407057	1991-01-01
EPX412426	1991-02-01
EPX437377	1991-07-01
EPX448798	1991-10-01
EPX499491	1992-08-01
EPX507622	1992-10-01
EPX509670	1992-10-01
EPX517243	1992-12-01
EPX518230	1992-12-01
EPX530400	1993-03-01
EPX536440	1993-04-01
EPX558318	1993-09-01
EPX558316	1993-09-01
EPX647435	1995-04-01
EPX653192	1995-05-01
EPX674909	1995-10-01
EPX684015	1995-11-01
EPX688536	1995-12-01
EPX694290	1996-01-01
EPX692224	1996-01-01
EPX697199	1996-02-01
EPX709065	1996-05-01
EPX714635	1996-06-01
EPX717967	1996-06-01
EPX733345	1996-09-01
EPX732080	1996-09-01
EPX737447	1996-10-01
EPX740926	1996-11-01
EPX754437	1997-01-01
FRX57862	1953-09-01
FRX1215305	1960-04-01
FRX1454773	1966-10-01
FRX2313949	1977-01-01
FRX2443829	1980-07-01
FRX2501034	1982-09-01
FRX2645008	1990-10-01
DEX651428	1937-09-01
DEX1007960	1957-05-01
DEX2222820	1973-11-01
DEX2457900	1976-05-01
DEX2930982	1981-02-01
DEX3209444	1982-10-01
DEX3215832A	1982-11-01
DEX3119735	1983-01-01
DEX3245570	1984-06-01
DEX222207	1985-05-01
DEX3427517	1986-01-01
DEX3423356	1986-01-01
DEX3511107	1986-10-01
DEX3623688	1987-01-01
DEX3530335	1987-03-01
DEX3707820	1987-09-01
DEX3622337C2	1988-01-01
DEX3642077C2	1988-06-01
DEX3708801C2	1988-09-01
DEX3824913	1990-02-01
DEX3838840C2	1990-05-01
DEX3930451	1991-03-01
DEX4108269C2	1992-06-01
DEX4103972C2	1992-08-01
DEX4126608	1993-02-01
DEX4139029C2	1993-06-01
DEX4217999A1	1993-12-01
DEX4237321A1	1994-05-01
DEX4323585	1995-01-01
DEX4339049	1995-05-01
DEX4425015	1996-01-01
DEX4429478	1996-03-01
DEX19530004	1996-03-01
DEX19512640C2	1996-10-01
DEX19514552	1996-10-01
DEX19514553C1	1996-10-01
DEX19510185	1996-10-01
DEX19526244	1997-01-01
DEX19543547C1	1997-01-01
DEX19526243C1	1997-01-01
DEX29617461U	1997-02-01
DEX19630601	1997-02-01
DEX19537897	1997-03-01
DEX19542419	1997-05-01
DEX19542417	1997-05-01
DEX19542418	1997-05-01
DEX19650797	1997-06-01
DEX19545756	1997-06-01
DEX19545539	1997-06-01
JPX62-211060	1987-09-01
CHX243478	1946-07-01
SUX644491	1979-01-01
GBX1361497	1974-07-01
GBX2037167	1980-07-01
GBX1583397	1981-01-01
GBX2084880	1982-04-01
GBX2101893	1983-01-01
GBX2133290	1984-07-01
GBX2145932	1985-04-01
GBX2161081	1986-01-01
GBX2164473	1986-03-01
GBX2165761	1986-04-01
GBX2177309	1987-01-01
GBX2179861	1987-03-01
GBX2213381	1989-08-01
GBX2214430	1989-09-01
GBX2269538	1994-02-01
WOXWO81/03271	1981-11-01
WOXWO82/00084	1982-01-01
WOXWO84/03829	1984-10-01
WOXWO88/01851	1988-03-01
WOXWO90/03152	1990-04-01
WOXWO93/08756	1993-05-01
WOXWO93/13816	1993-07-01
WOXWO93/13718	1993-07-01
WOXWO93/16650	1993-09-01
WOXWO93/20877	1993-10-01
WOXWO93/20747	1993-10-01
WOXWO93/19682	1993-10-01
WOXWO93/19681	1993-10-01
WOXWO94/06410	1994-03-01
WOXWO94/04220	1994-03-01
WOXWO94/10925	1994-05-01
WOXWO94/10921	1994-05-01
WOXWO94/10924	1994-05-01
WOXWO94/23659	1994-10-01
WOXWO94/26228	1994-11-01
WOXWO94/28809	1994-12-01
WOXWO95/02369	1995-01-01
WOXWO95/05781	1995-03-01
WOXWO95/10321	1995-04-01
WOXWO95/10320	1995-04-01
WOXWO95/09577	1995-04-01
WOXWO95/09576	1995-04-01
WOXWO95/19733	1995-07-01
WOXWO95/18575	1995-07-01
WOXWO95/17855	1995-07-01
WOXWO95/20360	1995-08-01
WOXWO95/24160	1995-09-01
WOXWO95/25472	1995-09-01
WOXWO95/23558	1995-09-01
WOXWO95/26686	1995-10-01
WOXWO95/30377	1995-11-01
WOXWO95/31144	1995-11-01
WOXWO96/00528	1996-01-01
WOXWO96/00042	1996-01-01
WOXWO96/00043	1996-01-01
WOXWO96/00036	1996-01-01
WOXWO96/00039	1996-01-01
WOXWO96/00040	1996-01-01
WOXWO96/04859	1996-02-01
WOXWO96/09010	1996-03-01
WOXWO96/07360	1996-03-01
WOXWO96/11638	1996-04-01
WOXWO96/10367	1996-04-01
WOXWO96/14021	1996-05-01
WOXWO96/14020	1996-05-01
WOXWO96/19152	1996-06-01
WOXWO96/18349	1996-06-01
WOXWO96/24301	1996-08-01
WOXWO96/24296	1996-08-01
WOXWO96/23448	1996-08-01
WOXWO96/23449	1996-08-01
WOXWO96/27337	1996-09-01
WOXWO96/32897	1996-10-01
WOXWO96/29946	1996-10-01
WOXWO96/34571	1996-11-01
WOXWO96/34570	1996-11-01
WOXWO96/34567	1996-11-01
WOXWO96/37146	1996-11-01
WOXWO96/39967	1996-12-01
WOXWO96/39966	1996-12-01
WOXWO96/39089	1996-12-01
WOXWO96/38094	1996-12-01
WOXWO96/39085	1996-12-01
WOXWO96/39086	1996-12-01
WOXWO96/39088	1996-12-01
WOXWO97/00647	1997-01-01
WOXWO97/00646	1997-01-01
WOXWO97/24994	1997-07-01
WOXWO97/24993	1997-07-01
WOXWO96/34569	1999-11-01

Non-Patent Literature (50)

Cook, Albert M. & John G. Webster, Therapeutic Medical Devices Application and Design, Prentice-Hall Inc., New Jersey, 1982, p. 349.
Pearce, John A., Electrosurgery, John Wiley & Sons Inc., New York, 1986, pp. 17, 69-75 and 87.
Wyeth, G.A., Electrosurgical Unit, pp. 1180-1202.
Everest Medical Technologies, Inc., "Everest Bipolar Laparoscopic Cholecystectomy," Transcript of Lecture by Dr. Olsen, Oct. 7, 1991.
Dobbie, A.K., "The Electrical Aspects of Surgical Diathermy," Biomedical Engineering, May 1969, pp. 206-216.
Valleylab, Excerpts from Valleylab SSE2L Instruction Manual, Valleylab Part No. A 945 110 005 H, Jan. 6, 1983.
Schurr, M. O. et al., "Histologic Effects of Different Technologies for Dissection in Endoscopic Surgery:Nd:YAG Laser, High Frequency and Water-Jet," End. Surg., vol. 2, 1994, pp. 195-201.
Newman, Laura, "Could Twist on TURP Knock Lasers Out," Urology Times, vol. 3, No. 3, Mar. 1995, p. 21.
ArthroCare Corporation, "The Arthrocare Arthroscopic System," 1995.
Tucker, R.D. et al., "In Vivo Effect of 5 French Bipolar and Monopolar Electro-Surgical Probes on Porcine Bladder," Urological Research, Springer-Verlag 1990, 18:291-294.
Kramolowsky, Eugene V. et al., "The Urological Application of Electrosurgery," The Journal of Urology, vol. 146, Sep. 1991, pp. 669-674.
Tucker, Robert D. et al., "A Comparison of Urologic Application of Bipolar Versus Monopolar Five French Electrosurgical Probes," The Journal of Urology, vol. 141, Mar. 1989, pp. 662-665.
Kramolowsky, Eugene V. et al., "Use of 5F Bipolar Electrosurgical Probe in Endoscopic Urological Procedures," The Journal of Urology, vol. 143, Feb. 1990, pp. 275-277.
Tucker, Robert et al., A Bipolar Electrosurgical TURP Loop, Abstract of Paper P14-11, 7.sup.th World Congress on Endourology and ESWL, Nov. 27-30, Kyoto, Japan, 1989, p. 248.
Ramsay, J.W. A. et al., "A Comparison of Bipolar and Monopolar Diathermy Probes in Experimental Animals," Urological Research, Springer-Verlag 1985, 13:99-102.
German Article w/ Translation: Elsasser, E. adn Roos, E., "Concerning an Instrument for Transurethral Resection without Leakage of Current," Medizinal-Marks/Acta Medicotechnica, vol. 24, No. 4, 1976, pp. 129-134.
Nardella, Paul C., "Radio Frequency Energy and Impedance Feedback," SPIE, vol. 1068, Catheter-Based Sensing & Imaging Technology, 1989, pp. 42-48.
Honig, William M., "The Mechanism of Cutting in Electrosurgery," IEEE Transactions on Biomedical Engineering, Jan. 1975, pp. 58-65.
Barry, Kevin J. et al., "The Effect of Radiofrequency-Generated Thermal Energy on the Mechanical and Histological Characteristics of the Arterial Wall In Vivo: Implications for Radiofrequency Angioplasty," American Heart Journal, vol. 117, No. 2, Feb. 1989, pp. 332-341.
Slager, Cornelis J. et al., "Vaporization of Atherosclerotic Plaques by Spark Erosion," Journal of American College of Cardiology, 1985, pp. 1382-1386.
Lee, Benjamin I. et al., "Thermal Compression and Molding of Atherosclerotic Vascular Tissue with Use of Radiofrequency Energy: Implications for Radiofrequency Balloon Angioplasty," Journal of American College of Cardiology, vol. 13, No. 5, Apr. 1989, pp. 1167-1175.
Piercey, J.R.A. et al., "Electrosurgical Treatment of Experimental Bleeding Canine Gastric Ulcers," Gastroenterology, vol. 74, No. 3, 1978, pp. 527-534.
Protell, Robert L. et al., "Computer-Assisted Electrocoagulation: Bipolar vs. Monopolar in the Treatment of Experimental Canine Gastric Ulcer Bleeding," Gastroenterology, vol. 80, No. 3, 1981, pp. 451-455.
Johnston, James H. et al., "Experimental Comparison of Endoscopic Yttrium-Aluminum-Garnet Laser, Electrosurgery, and Heater Probe for Canine Gut Arterial Coagulation," Gastroenterology, vol. 92, No. 5, May 1987, pp. 1101-1108.
Dennis, M.B. et al., "Evaluation of Electrofulguration in Control of Bleeding of Experimental Gastric Ulcers," Digestive Diseases and Sciences, vol. 24, No. 11, Nov. 1979, pp. 845-848.
Silverstein, Fred E. et al., "Endoscopic Hemostasis Using Laser Photocoagulation and Electrocoagulation," Digestive Diseases and Sciences, vol. 26, No. 7, Jul. Supplement 1981, pp. 31s-40s.
Auth, D.C., "Animal Testing of Endoscopic Hemostasis with Lasers and Other Devices," Endoscopy, vol. 18, Supplement 2, May 1986, pp. 36-39.
McLean, A. J., "The Bovie Electrosurgical Current Generator--Some Underlying Principles and Results," Archives of Surgery, vol. 18, 1929, pp. 1863-1873.
McLean, A. J., "Characteristics of Adequate Electrosurgical Current," American Journal of Surgery, vol. XVIII, No. 3, Feb. 16, 1932, pp. 417-441.
Wattiez, Amaud et al., Electrosurgery in Operative Endoscopy, Blackwell Science Ltd., London, 1995, pp. 87-93, 155-163.
Farin, G., "Pneumatically Controlled Bipolar Cutting Instrument," End. Surg., 1993, pp. 1-3.
Muller, W., "The Advantages of Laparoscopic Assisted Bipolar High-Frequency Surgery," End. Surg., 1993, pp. 1-6.
Reidenbach, H. D., "Fundamentals of Bipolar High-Frequency Surgery," End. Surg. 1993, pp. 85-90.
Penketh, Richard et al., "Clinical Evaluation of the Procision Bipolar Electrosurgical Generator During Laparoscopic Gynaecological Procedures," EAES, 2nd International Congress of the European Association for Endoscopic Surgery, Madrid, Sep. 15-17, 1994.
Lloyd, David M. et al., "A New Portable Bipolar Generator-Use in Laparoscopic Cholecystectomy," EAES, 2.sup.nd International Congress of the European Association for Endoscopic Surgery, Madrid, Sep. 15-17, 1994.
Buchelt, Martin et al., "Excimer Laser Ablation of Fibrocartilage: An In Vitro and In Vivo Study," Lasers in Surgery and Medicine, vol. 11, 1991, pp. 271-279.
Srinivasan, R., "Ablation of Polymers and Biological Tissue by Ultraviolet Lasers," Science, vol. 234, Oct. 31, 1986, pp. 559-565.
Pearce, John A., "Chapter 3 Electrosurgery," Handbook of Biomedical Engineering, Ed. Jacob Kline, Academic Press, Inc., 1988, pp. 99-113.
Selikowitz, Stuart M. et al., "Electric Current and Voltage Recordings on the Myocardium During Electrosurgical Procedures in Canines," Reprint from Surgery, Gynecology & Obstetrics, Mar. 1987, vol. 164, pp. 219-224.
Tucker, Robert D. et al., "Demodulated Low Frequency Currents from Electrosurgical Procedures," Surgery, Gynecology & Obstetrics, Jul. 1984, vol. 159, pp. 39-43.
Lu, David Y. et al., "Electrical Thermal Angioplasty: Catheter Design Features, In Vitro Tissue Ablation Studies and In Vivo Experimental Findings," Am J Cardiol, vol. 60, 1987, pp. 1117-1122.
Malis, Leonard I., "Electrosurgery: Technical Note," J. Neurosurg., vol. 85, 1996, pp. 970-975.
Slager, C. J. et al., "Spark Erosion of Arteriosclerotic Plaques," Kardiologie, vol. 76, Suppl. 6, 1987, pp. 67-71.
Geddes, Leslie A., Medical Device Accidents--With Illustrative Cases, CRC Press, New York, 1998, p. 93 (commentary on Honig, William M., "The Mechanism of Cutting in Electrosurgery," IEEE Transactions on Biomedical Engineering, Jan. 1975, pp. 58-65).
Valleylab, Inc., "Force Electrosurgical Generators Instruction Manual," Valleylab Part No. 945 110 039 A, Feb. 1987, pp. 59-62.
Valleylab, Inc., "Advances in Bipolar Electrosurgery for Laparoscopic Surgery," Advances in Bipolar Electrosurgery, pp. 1-4.
Description of Codman and Johnson & Johnson Malis CMC-III Bipolar System.
Pfizer/Valleylab Press Release "Valleylab Inc. Introduces The Procision Bipolar Electrosurgery System," Sep. 15, 1994.
ArthroCare Corporation, "ArthroCare Arthroscopic Electrosurgery System, Model 970 Operator's Manual", Feb. 1996.
ArthroCare Corporation, "Arthroscopic Electrosurgery System, System 2000 Operator's Manual," Jan. 1998.

Abstract

Description