DE202014002143U1 - Systems related to electrosurgical pens - Google Patents

Abstract

An electrosurgical pen comprising: an elongated housing defining a handle end and a distal end; a hose member connected to the elongated housing; a spacer made of non-conductive material located at the distal end; a conductive electrode disposed on the spacer and defining an outer periphery; a first passage defined at least in part by the spacer, the first passage having a fluid connection to the hose member; the first passage defining a distal cross-section; and wherein the first passage defines a proximal cross-section that is closer to the handle end than the distal cross-section along a flow path, and wherein the distal cross-section is smaller than the proximal cross-section.

Description

CROSS-REFERENCE TO RELATED PATENT APPLICATIONS

This patent application claims the benefit of US Provisional Patent Application No. 61 / 773,917 filed March 7, 2013, entitled "Method and Systems Related to Electrourgical Wands."

BACKGROUND

Physicians use electrosurgical systems to perform certain functions during surgical procedures. For example, electrosurgical systems in ablation mode use high frequency electrical energy to remove soft tissue, adipose tissue, or other tissue such as meniscal tissue, cartilage, or synovial tissue in a joint.

BRIEF DESCRIPTION OF THE DRAWINGS

For the detailed description of the embodiments, reference is made to the accompanying drawings:

1 shows an electrosurgical system according to at least some embodiments;

2a . 2 B and 2c 10 is a perspective view of the distal end of a pin according to at least some embodiments;

3a and 3b 10 is a cross-sectional view of the distal end of a pin according to at least some embodiments;

4a and 4b 10 is a perspective view of the distal end of a pin according to at least some embodiments;

5 shows a side view of the distal end of a pin according to at least some embodiments;

6 10 is an exploded view of the distal end of a pin according to at least some embodiments;

7 shows a block diagram of an electrosurgical control unit according to at least some embodiments;

8th shows a method according to at least some embodiments; and

9 shows a method according to at least some embodiments.

NAMES AND TERMINOLOGY

Throughout the following description and the entire following claims, specific terms are used for individual system components. One skilled in the art will appreciate that companies that design and manufacture electrosurgical systems may refer to components by different names. This document does not distinguish between components whose function is identical but which use different names.

In the following description and the following claims, the terms "including" and "comprising" are used without limitation and therefore should be understood as including "but not limited to ...". Furthermore, the term "connect" refers to an indirect or direct connection. Thus, when a first device is connected to a second device, it may be a direct connection or an indirect connection through other devices and connections.

When referring to a single element, this includes the possibility that this element exists multiple times. In particular, in this document and the appended claims, the singular forms "a," "an," "an," and "the," "the," and "include" the plural unless this is clearly excluded by the context , It should also be noted that any optional element should be excluded in the claims. This statement is an anticipated basis for the use of such exclusive terminology as "alone," "only" and the like. Ä. In connection with the mention of claims or use in a "negative" delimitation intended. Finally, it should be noted that all technical and scientific terms used in this document have the meaning to be understood by one of ordinary skill in the art to which this invention belongs, unless otherwise defined.

"Active electrode" refers to an electrode of an electrosurgical pencil that produces an electrically-induced tissue-altering effect when placed in contact with or in close proximity to tissue to be treated, and / or an electrode induced by a voltage generator Has tension.

"Active connection" means an electrical connection to a current transformer connected to an active electrode of an electrosurgical pencil is connected.

"Counter electrode" refers to an electrode of an electrosurgical pencil that provides a path for the flow of electrons with respect to an active electrode and / or an electrode of an electrosurgical pencil that does not itself produce an electrically-induced tissue-altering effect on tissue to be treated generated.

"Mating connector" means an electrical connection to a current transformer connected to a counter electrode of an electrosurgical pencil.

"Plasma" refers to a very high temperature ionized gas in vapor bubbles or in a vapor layer capable of electrical discharge. Electrosurgical systems and methods described herein may also be used in dissecting or resecting tissue from tissue samples ex vivo and in procedures performed on tissue foreign objects. In some examples, electrosurgical systems and methods can be used on lifeless tissue, for example on meat or on carcasses.

If a range of values is given, the invention applies to any intermediate value between the upper and lower limits of this range of values and any other value in this range. In addition, it is conceivable that any optional feature of the described inventive variants may be presented independently or in combination with one or more of the features described in this document and claimed therefor.

All topics mentioned in this document (eg, publications, patents, patent applications, and hardware) are incorporated by reference in their entirety, unless the subject conflicts with the subject of the present invention (in this case, the topic of the present invention). The elements referred to are provided solely for the purpose of disclosure prior to the date of the present application. Nothing herein may be construed as an admission that the present invention has no legal claim to anticipate such matter by virtue of any preceding invention.

DETAILED DESCRIPTION

Before describing the various embodiments in detail, it should be understood that this invention is not limited to the variations described herein, as various changes or modifications may be made and substitutions may be made by way of correspondence without departing from the spirit and scope of the invention , As those skilled in the art will appreciate upon reading this disclosure, each of the individual embodiments described and illustrated herein has individual components and features that can be readily separated from or combined with the features of the other embodiments without departing from the spirit and scope of the present invention , In addition, many modifications may be made to adapt a particular situation, material, composition of matter, process, or process measures or steps to the objectives and spirit and scope of the present invention. All such modifications are intended to be within the scope of the claims set forth in this document.

In 1 becomes an electrosurgical system 100 illustrated according to at least some embodiments. The electrosurgical system 100 consists of an electrosurgical pencil 102 (hereafter "pen 102 ' ), with an electrosurgical control unit 104 (hereinafter "control unit 104 ) connected is. The pencil 102 consists of an elongated housing or shaft 106 , the or the distal end 108 Are defined. The elongated shaft 106 defines a handle or the proximal end 110 on which a doctor uses the pen during surgical procedures 102 holds. The pencil 102 also has an elastic multi-core cable 112 on, one or more electrical lines (not in 1 shown), and the elastic multi-core cable 112 ends in a pin connector 114 , As in 1 shown is the pen 102 with the control unit 104 connected, z. B. via the control unit connector 120 on the outer surface of the housing 122 (in the illustration in 1 the front).

Although in 1 not pictured, the pen points 102 in some embodiments, one or more internal fluid conduits connected to the externally accessible tubing members. As shown in the figure, the pen has 102 via an elastic hose element 116 that the suction at the distal end 108 of the pen. According to various embodiments, the hose element is 116 with a peristaltic pump 118 connected in 1 as integral with control unit 104 is pictured. In other embodiments, a housing for the peristaltic pump 118 from the case 122 for the control unit 104 be separated (as indicated by the dashed lines in the figure), however, is the Peristaltic pump in any case functionally with the control unit 104 connected. In the different embodiments, the peristaltic pump generates 118 at the distal end 108 of the pen 102 a volume-controlled suction from the surgical field.

In 1 is in the case 122 the control unit 104 a display or a user interface 130 Visible, and in some embodiments, a user can use the user interface 130 and the associated keys 132 Operating modes of the control unit 104 choose. In some embodiments, the electrosurgical system includes 100 also a foot pedal group 134 , The foot pedal group 134 can have one or more pedals 136 and 138 , an elastic multi-core cable 140 and a pedal connector 142 include. In the figure are only two pedals 136 and 138 but one or more pedals can be implemented. The housing 122 the control unit 104 can a corresponding connection part 144 having, with the pedal connector 142 connected is. A doctor can use the foot pedal group 134 different aspects of the control unit 104 , z. B. the operating mode, control. For example, the pedal 136 used to the application of high frequency energy (HF) to the pen 102 switch on and off. In addition, the pedal can 138 can be used to control and / or activate the ablation mode of the electrosurgical system. In certain embodiments, the control of the various functional or operational aspects of the control unit may 104 by selectively pressing the buttons on the handle 110 of the pen 102 be activated (the keys are not shown in order not to unduly increase the complexity of the figure).

The electrosurgical system 100 may have different modes of operation in the different embodiments. In one of these modes the Coblation ^® technology is used. The Bevollmächtige for the present disclosure is the owner ^® on the rights of Coblation technology. Coblation ^® technology involves the application of RF energy between one or more active electrodes and one or more counter electrodes of the stylus 102 to generate a high electric field strength near the target tissue. The electric field strength may be sufficient to vaporize an electrically conductive liquid over at least a portion of one or more active electrodes in the region between them and the target tissue. The electrically conductive liquid may be inherently present in the body, such as. Blood, or in some cases extracellular or intracellular fluid. In other embodiments, the electrically conductive liquid may be isotonic saline or a gas may be used.

In some embodiments, the electrically conductive liquid passes through the pin 102 delivered in the vicinity of the active electrodes and / or the target position.

When the temperature of the electrically conductive liquid is increased so much that the atoms of the liquid evaporate faster than the atoms condense, a gas is formed. When enough energy is applied to the gas, the atoms collide with each other; this causes a release of electrons and an ionized gas or plasma is formed (the so-called fourth state of matter). In other words, plasma can be generated by heating a gas and either passing an electrical current through the gas for ionization or directing electromagnetic waves into the gas. In the plasma formation processes, free electrons are directly supplied to free electrons in the plasma, electron-atom collisions release further electrons, and the process continues cascading until the desired electron density is reached. A more comprehensive description of plasma physics offers "Introduction to Plasma Physics" by RJ Goldston and PH Rutherford of the Plasma Physics Laboratory of Princeton University (1995) , The entire content of this book is incorporated by reference in its entirety.

When the density of the plasma is sufficiently low (ie less than about 1020 atoms / cm ³ for aqueous solutions), the mean free path of the electrons increases, so that subsequently injected electrons cause collision ionization in the plasma. When the ion particles in the plasma layer have sufficient energy (eg 3.5 eV (electron volts) to 5 eV), the collision of ion particles with molecules making up the target tissue breaks up molecular bonds and the molecules become free radicals which then combine to form gaseous or liquid molecules. Frequently, the electrons in the plasma carry the electric current or they absorb the electromagnetic waves and therefore have a higher temperature than the ion particles. Therefore, the electrons that pass from the target tissue to the active or counter electrodes carry the majority of the heat of the plasma so that the ion particles can break up the target tissue molecules with substantially no heat.

By means of molecular splitting (as opposed to thermal evaporation or carbonization), the target tissue is formed by splitting larger organic molecules into smaller molecules and / or atoms, e.g. As hydrogen, oxygen, carbon oxides, hydrocarbons and nitrogen compounds, volumetrically removed. By the Molecular cleavage completely removes the tissue structure, while in related art electrosurgical desiccation and vaporization techniques, the tissue is dehydrated by removing the fluid in the tissue cells and the extracellular fluids. The jointly transmitted U.S. Patent No. 5,697,882 , whose entire content is incorporated by reference in its entirety, contains a more detailed description of the molecular breakdown.

In addition to the Coblation ^® mode is the electrosurgical system 100 in 1 also useful for occluding larger arterial vessels (eg, on the order of about 1 millimeter (mm) in diameter) when used in the so-called coagulation mode. The system in 1 may thus have an ablation mode in which RF energy having a first voltage sufficient to effect the molecular splitting or degradation of the tissue is applied to one or more active electrodes and the system in FIG 1 may also have a coagulation mode in which RF energy having a second, lower voltage sufficient to heat, shrink, fuse, and / or achieve segregation of severed vessels in the tissue, to one or more active electrodes (either the same electrode (s) as in the ablation mode or (a) other electrode (s)) is applied.

The electrosurgical system 100 at the distal end 108 of the pen 102 generated energy density can be varied by adjusting a number of factors, for example: number of active electrodes; Electrode size and spacing; Electrode surface; Unevenness and / or sharp edges on the electrode surfaces; Electrode materials; applied voltage; Limiting the current of one or more electrodes (eg, by switching a coil in series with an electrode); electrical conductivity of the liquid in contact with the electrodes; Density of the conductive liquid; and other factors. These factors can be manipulated to control the energy level of the excited electrons.

2a . 2 B and 2c show a perspective view of the distal end 108 of the pen 102 according to example systems. In the illustrated embodiment, the elongated shaft 106 made of metal (eg TP304 stainless steel tube for subcutaneous application), and in some cases defines the elongated shaft 106 also a counter electrode for the system. As shown in the figure, the elongated shaft 106 a circular cross section at least at the distal end 108 define. The in 2c shown pen 102 with a circular cross-section and the active electrode 202 at an angle of 90 ° to the axis of the shaft 106 may be particularly suitable for surgical procedures on the shoulder, where the space in which the pen is inserted, is not limited. However, in some embodiments, e.g. As with pins for surgical procedures on the knee, the cross section of the elongated shaft 106 an oval, where the active electrode 202 an angle of 50 ° to the axis of the shaft 106 in order to allow a lower profile of the distal end of the pen, thus taking into account space constraints and facilitating access to the back of the knee (see 2 B ). In embodiments in which the cross section of the elongate shaft 106 Circular, the outer diameter may be about 3 millimeters (mm), but it can also be used larger and smaller dimensions. In embodiments in which the cross section of the elongate shaft 106 is more oval, a larger comparable surface of the active electrode 202 provided. The largest outer diameter may be about 3 mm and the smallest outer diameter about 2 mm, but larger and smaller dimensions can also be used here.

In embodiments in which the elongate shaft is made of metal, the distal end may be 108 also a non-conductive spacer 200 included with the elongated shaft 106 connected is. In some cases, this is the spacer 200 made of ceramic, other non-conductive materials, which are resistant to decomposition on contact with plasma, can be used equally (eg glass). The spacer 200 Can in any suitable way with the elongated shaft 106 be connected, for. B. by telescoping within the elongated shaft 106 (as shown), by telescoping over the elongated shaft 106 and / or with adhesive. The spacer 200 carries at least one active electrode 202 which is made of metal. The spacer 200 thus isolates the active electrode 202 electrically from the elongated shaft 106 which can act as a counter electrode. In other embodiments, only a portion of the elongated shaft is 106 exposed to as a counterelectrode 203 to act.

The illustrative active electrode defines an exposed outer surface 204 as well as an inner surface (in 2a - 2c not visible), attached to the spacer 200 borders. In some embodiments, e.g. B. the in 2 B , the active electrode defines an exposed edge surface 205 to provide an ablative lateral effect on certain more sensitive tissue types, e.g. As cartilage to allow. The active electrode 202 also includes at least one passage 206 , which has a fluid connection with the elastic hose member 116 (in 2a - 2c not shown). The spacer 200 also has a passage 208 on, also via a fluid connection with the elastic hose element 116 features. As shown, the passages are 206 and 208 at least partially aligned so that liquid and / or tissue can be drawn through the passages in a liquid conduit in the elongated shaft. Below are different relationships of the passages 206 and 208 described.

Implementing a system with volume-controlled suction through the passages allows much larger passages than related art. Due to insufficient vacuum control by the related art vacuum sources, in related art pins, by limiting the exhaust ports, attempts are made to impose upper limits on the flow of fluids. For example, in related art, a diameter of 0.75 mm of a circular passage is the upper limit for the passage diameter. However, in the various embodiments, since the volume flow is controlled by other mechanisms, the control of the volume flow allows much larger passages. For example, in illustrative embodiments with a circular passage 206 the diameters are 0.79 mm to 1.4 mm (inclusive), and in one particular embodiment 1.2 mm. As explained below, in addition, the diameter of the illustrative circular passage in the spacer 200 larger than the diameter of the passage 206 be. The passage 206 can have various additional forms, for. B. in certain embodiments, a star shape or star shape (see 2c ).

As in 2a - 2c It may be helpful in some electrosurgical example procedures to demonstrate the ability of the active electrode 202 to restrict physical contact with the target tissue. In such cases, at the distal end 108 of the pen 102 one or more standoffs are implemented. In the specific embodiment, which is in 2a and 2 B are shown are four spacers 210 . 212 . 214 and 216 displayed. Each standoff is made of non-conductive material, for. B. the same material as the spacer 200 , In some cases, the spacers are 210 . 212 . 214 and 216 integral with the spacer 200 manufactured (ie, the spacer and the spacer bolts are a single element), in other cases, however, the standoffs are made separately and with the spacer 200 connected. The active electrode 202 defines an outer outline 218 and the illustrative standoffs are immediately on the outer contour 218 arranged (for example, at a distance of 0.1 mm from the outer contour 218 ). In some cases, the standoffs abut the outer contour.

In accordance with at least some embodiments, the standoffs provide 210 . 212 . 214 and 216 a predefined distance above the outer surface 204 the active electrode 202 , For example, assume the outer surface 204 the active electrode 202 defines a level. In at least some embodiments, the standoffs protrude 210 . 212 . 214 and 216 at least 0.1 mm above the plane defined by the outer surface of the active electrode. Longer or shorter projections over the through the outer surface 204 the active electrode 202 defined levels are also considered.

While in some cases the standoffs are the outer contour 218 the active electrode 202 In other cases, the standoffs may have gaps or recesses. In the illustrative case in 2a There are four such gaps 220 . 222 . 224 and 226 shown. The inventors of the present specification have found that such gaps assist various aspects of the surgical procedures without the ability of the standoffs 210 . 212 . 214 and 216 to significantly reduce the likelihood that the active electrode will directly contact the tissue at the target site. The length of each cutout, or alternatively formulated, the amount of length with which the standoffs 210 . 212 . 214 and 216 Surrounding the electrode may be different for each pen. In some cases, however, the standoffs surround at least 25% of the outer contour 218 the active electrode 202 and in the figure about 40% of the outer contour 218 the active electrode 202 , In addition, the spacers can 210 . 212 . 214 and 216 in some cases the active electrode 202 before washing out the plasma, which is on a section of the active electrode 202 has formed, by the suction flow in the direction of the passage 206 Protect by passing the flow over some areas of the screen of the active electrode 202 is redirected.

3a shows a sectional drawing (along the line 3-3 of 2a ) of the distal end 108 of the pen 102 according to at least some embodiments. 3a shows in particular the on the spacer 200 adjacent active electrode 202 , The spacer 200 is in the elongated housing 106 telescoped, and in some cases, the spacer may at least partially with an adhesive 300 be attached. 3a also shows the passage 206 through the active electrode 202 as well as the passage 208 through the spacer 200 , As in 3a but defines the passage 208 according to example systems a distal section 302 and a proximal section 304 , The distal section 302 defines a cross section (eg a cross section perpendicular to the central axis 306 ), which is smaller than the cross section of the proximal section 304 (eg also perpendicular to the central axis 306 ). In the illustrative case of the distal section 302 and the distal portion 304 defining circular passages defines the distal section 302 a circular through-hole with the diameter D1, and the proximal portion 304 defines a circular through-hole of diameter D2, where D2 is greater than D1. The spacer 200 also defines the axial length L1, while the proximal portion 302 the axial length L2 and the distal portion 304 defines the axial length L3. The transition 308 between the distal section 302 and the proximal portion 304 (ie, the shoulder region) has a rectangular cross section in the figure. Less abrupt transitions 308 However, are also considered, for. B. a transition defining a conical truncated cone (shown by dashed lines).

In accordance with at least some embodiments, the combination creates the distal portion 302 and proximal section 304 a constriction in close proximity to the active electrode 202 (and thus to the plasma). The through the interaction of the distal section 302 and the proximal portion 304 Constriction illustrated illustrates a functional philosophy implemented in example systems. In particular, in the related art functional philosophy, the goal of tissue ablation has been to create tissue particles that are substantially smaller than the smallest inside diameter in the suction path to avoid clogging of the suction passage and / or suction lumen (ie, suction path). For this reason, many related art devices use metal screens over the passage to create the plasma to create the small tissue particles. In contrast to the related art philosophy of operation, the example systems described in this specification operate in accordance with the philosophy that the tissue must be divided into particles small enough to pass through the distal section 302 of the passage 208 caused narrowing to happen. The passage 208 will be behind the distal section 302 opened or expanded, and when the tissue through the distal section 302 it can pass through the entire suction path without clogging it.

The functional philosophy is represented by the cross-section of the passage 206 supported in the active example electrode. In particular and as shown is the cross section of the passage 206 smaller than the distal section 302 of the passage 208 , As in the illustrative case the passage 206 is circular or star-shaped, is the diameter D3 of the passage 206 smaller than the diameter D1 of the distal portion 302 of the passage 208 , Therefore, a piece of fabric need only be small enough to pass through in any two dimensions 206 to pass (eg the smallest two dimensions in an elongate piece of fabric), and in the subsequent transport of the fabric through the Absaugpfad occur only larger cross-sections. However, it should be noted that the active electrode 202 is exposed to an etching effect during use and therefore the cross section of the passage 206 the longer the pen, the larger it gets 102 is used in plasma mode. In most cases, the expected useful life of a pen is known in advance, and the cross section of the port 206 is chosen to be less than or equal to the cross section of the distal portion at the end of the expected usage time 302 of the passage 208 is.

According to the example systems, the difference between the cross section of the distal section 302 and the proximal portion 304 one percent (1%) to thirty percent (30%) (inclusive), and in a given case at least twenty percent (20%). In illustrative embodiments, where both the passageway 206 in the active electrode 202 as well as the passage 208 can be circular, the initial diameter of the passage 206 about 1.2 mm, the diameter of the distal section 302 about 1.4 mm and the diameter of the proximal section 304 about 1.65 mm. The total length of the spacer 200 may be different for pins intended for different surgical procedures (eg, knee or shoulder), but in some cases, the overall axial length L1 of the spacer may be in the range of 2.0 mm to 3.0 mm and the axial Length L3 of the distal section 302 in the range of 1.0 mm to 1.5 mm. Other sizes can be used equally. In addition, the internal configuration of the spacer 200 for different pen configurations (eg, pens for the shoulder, with the electrode 202 an angle of 90 to the axis of the shaft 106 ), wherein the passage 206 transverse to the central axis 306 is aligned so that the distal section 302 at the passage 206 and the proximal section 304 at the central axis 306 is aligned. In particular, in these configurations, the use of the conical transition 308 which is the right angle between the distal section 302 and the proximal portion 304 bridged, an advantage.

Because the control unit 104 and in particular the peristaltic pump 118 control the volume flow in the pen, the different dimensions of the ports can be considered as alternatives to provide different flow rates in each section. To work with the peristaltic pump 118 To achieve a constant volume flow of the fluid, according to the laws of hydrodynamics, the velocity of fluid (and tissue) must pass when passing each Be different passage. Thus, due to the relationships between the cross sections of the passage 206 and the sections of the passage 208 the flow rate of fluid through each passageway differs to that at the peristaltic pump 118 to achieve a constant volume flow. For example, based on the relationships of the cross sections described above, the flow rate of fluid through the distal portion is 302 between one percent (1%) and thirty percent (30%) faster than flow rate through the proximal section 304 and in some cases at least twenty percent (20%) faster. In addition, for the same constant volume flow, the velocity is in the passage 206 through the active electrode 202 faster than through the distal section 302 of the passage 208 , However, here too, the speed passes through the passage 208 the speed through the distal section 302 approximates when the passage 206 becomes larger due to the etching effect. Initially, however, the speed of passing through 206 flowing fluid at least ten percent (10%) faster than the speed through the distal section 302 be.

In the embodiments described so far for the pen 102 It was assumed that the cross-sectional shape of the passage 206 with the cross-sectional shape of the distal portion 302 of the passage 208 exactly or approximately matches and that also the cross-sectional shape of the distal section 302 of the passage 208 with the cross-sectional shape of the proximal portion 304 of the passage 208 matches. However, in other embodiments, the cross-sectional shapes of the various passages do not have to match. For example, the passage 206 have a circular cross-section, while section 302 and 304 of the passage 208 define a quadrilateral (eg square, rectangle). So z. B. the passage 206 have a star-shaped cross section, while section 302 and 304 of the passage 208 can each define a circular cross-section. In addition, section must 302 and 304 of the passage 208 also do not define the same cross-sectional shape. Therefore, in some cases, the size differences of the passages can be expressed as the largest measure along a straight line. For example, in some cases, the largest amount of the passage 206 in the conductive electrode 202 between one percent (1%) and twenty percent (20%) smaller than the largest dimension of the distal section 302 of the passage 208 and in a given case at least fifteen percent (15%) smaller.

3a also shows an illustrative electrical connection of the active electrode 202 , In particular, the active electrode defines 202 an inner surface 310 attached to the distal end of the spacer 200 borders. The illustrative active electrode 202 also defines elbows inserted in counterbores of the spacer. For example, the active electrode defines the elbow 312 that in the counterbore 314 of the spacer is inserted. In some cases, this is the elbow piece 312 by press fit in the counterbore 312 attached, in other cases, however, may be an adhesive 316 to be used. Because the bow piece 312 has no electrical connection, the connection of the elbow can 312 with the spacer 200 only mechanical support for the active electrode 202 provide so that the active electrode continues to the spacer 200 borders. 3a also shows the bow piece 318 that into the hole 320 is used. As before, an adhesive can also be used 322 for fixing the elbow piece 318 be present in the hole. In contrast to the bow piece 312 is the bow piece 318 however with an insulated wire 324 electrically connected by the bore 320 leads. Thus, for the active electrode 202 provided energy through the insulated wire 324 be transmitted. Therefore, with regard to the elbow piece 318 the adhesive 322 not only provide mechanical support, but also the bore 320 close.

3b also shows an alternative electrical connection of the active electrode 202 , The electric wire 324 leads through the shaft 106 and the hole 320 in the distance piece 200 to the active electrode 202 to electrically connect them. The active electrode 202 is at the distance piece 200 attached, leaving a section 326 the vein 324 through passages in the active electrode 202 and the hole 320 leads. The section 326 may be about 0.006 inches to 0.015 inches or less above the surface of the vein 324 extend. The section 326 the vein 324 is laser welded and then forms on the surface of the active electrode 202 the seam 330 (see also 2 B ). The seam 330 comes with smooth transition sections 331 and 332 between the seam 330 and the active electrode 202 made to reduce the likelihood that the suture 330 the plasma formation at the transitional sections 331 and 332 promotes. The transition sections 331 and 332 do not have any rough surfaces, edges or other imperfections to prevent plasma formation on them. The seam 330 is used for electrical connection and mechanical fixing of the active electrode 202 at the distance piece 200 , In addition, during laser welding certain quantities 328 from section 326 the vein 324 into the passages of the active electrode 202 flow, so also in the passages of the active electrode 202 a mechanical and electrical connection between the active electrode 202 and the vein 324 he follows. In certain embodiments, using a Section length of vein 324 an exclusively mechanical connection for attaching the active electrode 202 at the distance piece 200 getting produced. In these configurations, the vein becomes 324 Bent in a U-shape, leaving the free ends of the vein 324 at the appropriate position through the active electrode 202 guided and then by laser welding to the active electrode 202 be attached. The present inventors have found that it is advantageous to use the active electrode 202 made of tungsten and the vein 324 made of titanium or platinum to match the bonding properties of the seam 330 to improve in this configuration. In addition, the inventors of the present specification have found that it is advantageous to use the various seams with which the active electrode 202 attached and connected to be arranged at positions that are different from the edges of the active electrode 202 and the passage 206 are removed to the wear of the seams 330 to reduce and increase their lifespan.

4a and 4b show a perspective view of a distal end 108 a pen 102 according to further example systems. 4a shows in particular the at the spacer 200 arranged active electrode 202 , 4a also shows the pilot electrode 201 in the groove 400 of the spacer 200 that are adjacent to the active electrode 202 is arranged, with channel 402 a connection with the groove 400 forms. The pilot electrode 201 is defined by a single, uninsulated wire, while the active electrode 202 is defined by a flat, shielded wire. The inventors of the present specification have found that a configuration with two or more electrodes of different sizes activated asynchronously may be beneficial to the electrosurgical effect. This configuration is in contrast to current systems that use only a single active electrode or multiple synchronously activated electrodes, the only way to reduce the amount of current dissipation is to reduce the size of the electrode (s) and / or reduce the amount of fluid flow over the electrode (s).

The principle of the configuration of two different size active electrodes described in the present embodiment is to control the electrode surface of the one active electrode that makes contact with the low impedance conductive liquid. This is done by activating two or more active electrodes sequentially and asynchronously separately over separate output channels. In doing so, sufficient vapor coverage is achieved on the first activated electrode before the next active electrode is activated. This prevents the conductive liquid from being exposed to a large area, and thus limits the general current dissipation. Accordingly, in the present embodiment, the pilot electrode 201 generally smaller than the active electrode 202 However, other relative sizes are contemplated that can be used equivalently. First, the Piloteletrode 201 Activates and generates, according to the electrosurgical principles described in this document, a vapor layer progressively migrating through the channel 402 the active electrode (s) 202 covered. Subsequently, the active electrode 202 be activated with a small delay. The delay can be controlled automatically by changing the impedance of the active electrode circuit 202 and the counter electrode 203 measured and the activation of the active electrode 202 is triggered when the measured impedance of the electrode circuit reaches a certain threshold. As described above, the smaller pilot electrode is 201 in the groove 400 positioned to prevent the vapor layer bubbles (ie the plasma) from being destroyed due to the flow of liquid over the tip of the object. Therefore, the stable activation of the pilot electrode remains 201 regardless of whether the active electrode 202 is activated. In cases where the vapor layer is on the active electrode 202 is destroyed and therefore the active electrode 202 completely exposed to the field of circulating conductive liquid and the current reaches a level which forces the deactivation of the RF output remains the pilot electrode 201 activated and the corresponding vapor layer is retained. The active electrode 202 can be activated if it is sufficiently covered with gas or steam to prevent unwanted current dissipation that occurs when plasma is destroyed.

In a related embodiment, the liquid flow becomes above the active electrode 202 through a peristaltic pump 118 (please refer 1 ) and the flow over the active electrode 202 is terminated or reduced until it is sufficiently covered with a gas or vapor layer. Restoration of the gas or vapor layer is accomplished by terminating the liquid flow over the active electrode 202 and / or by the presence of a continuous vapor layer on the adjacent pilot electrode 201 is formed, supported. To maximize the performance of the system according to these embodiments, the pilotselectrode must 201 and the active electrode 202 each be powered by an independent power supply or power amplifier, which also monitors the impedance of the electrode circuit. In some cases it may be helpful to use different active electrodes 202 to activate at different amplitudes or pulse widths to produce a vapor layer but at the same time increase the total amount of dissipated energy or dissipated current restrict so that only the active electrode (s) 202 is activated with a sufficiently high impedance of the electrode circuit (ie, indicative of a stable vapor layer on the surface of the respective electrode) of full amplitude and / or pulse width.

During arthroscopic surgical procedures, the field of view near the surgical site (ie, near the active electrode) may be obscured by gas bubbles. The ablation process produces gas bubbles, and in many cases, the gas bubbles are quickly sucked off so they do not affect the field of view. However, in some situations (eg, if the primary passageway is temporarily occluded by tissue), gas bubbles may form near the surgical site obscuring the field of view. The with regard to 5 Example pen described below 102 has additional features that reduce the accumulation of gas bubbles near the surgical site. In particular, the example features include slots in the active electrode, and in some cases, spacer defined flow channels forming passages near the outer contour of the active electrode. The slots are designed and manufactured so that essentially only gases are passed through the slots. That is, the size of the slits is chosen so that the tissue in the surgical field (even tissue that is released during ablation) is too large to pass through the slits. Likewise, the surface tension of liquids (eg, saline, blood, extracellular, and intracellular fluid) is too strong for fluids to pass through the slits. Therefore, only gases can be sucked through the slots. Thus, the slots do not interfere with the ablation characteristics of an active electrode, but in some situations may help to aspirate the bladders from the surgical field, especially if the primary passageway is completely or partially occluded.

5 shows a side view of the distal end of the pin 102 according to the other example systems. In particular shows 5 the elongated shaft 106 and the active electrode 202 attached to a spacer 200 of non-conductive material adjacent. The outer surface 204 the active electrode 202 in 5 defines a plane that is parallel to the central axis. In the example in 5 defines the elongated shaft 106 a central axis 500 , The through the outer surface 204 plane defined by the active electrode is parallel to the central axis 500 , The various features of the pen described below 102 in 5 however, are not limited to pins whose outer surface 204 parallel to the central axis 500 is, for example, for the in 2a and 2 B shown pins are used.

In 5 is the primary passage 502 through the active electrode 202 displayed. The passage 502 is at least partially at a passage through the spacer 200 (the passage through the spacer is in 5 not shown), and both the passageway 502 as well as the passage through the spacer 200 have a fluid connection to the elastic hose member 116 (also in 5 not illustrated). The primary example passage 502 in 5 has several bumps and these can aid in the initial formation of plasma. The passage 502 is for illustration only, and the above-described star-shaped and / or oval apertures may be used equivalently for the example pen in FIG 5 to be used.

The active electrode 202 in 5 also has several slots 504 on. Six of these slots are shown, but one or more slots are considered. Every slot 504 is a passageway through the active electrode 202 leads. The slots 504 however, serve the specific purpose of sucking bubbles in the vicinity of the electrode, and they are referred to in this patent as slits rather than passages to separate them from other passages (eg, the primary passage 502 in 5 or the primary passage 206 the previous example pens) logically. Each of the slots 504 is parallel to the outer outline 218 however, other arrangements of the slots are contemplated. In some cases, the distance D1 between each slot and the outer contour 218 of the active electrode is 0.008 to 0.010 inches (0.2032 to 0.254 mm) (inclusive). Thus, the slots are 504 closer to the outer outline 218 arranged as the passage 502 on the outer outline 218 is arranged. The example slots 504 are around the primary passage 502 arranged. For example, the slot 504A on one side of the passage 502 arranged while the slots 504C and 504D are arranged on an opposite side of the primary passage. The slot is corresponding 504B on one side of the passage 502 arranged on the side of the slot 504E opposite. In an example system (not shown) is a single slot 504 present, the passage 502 completely surrounds.

In the enlarged section 506 of the 5 is the slot 504C shown in more detail. Each slot defines a length L and a width B, and for each slot, the length L is at least twice the width B. The length L of a slot may be in the range of 0.002 inches (0.0508 mm) to a length that sufficient for the passage 502 completely surrounded. It should be noted that in the case where a single slot passes through 502 completely surrounds the outer surface 204 the active one electrode 202 possibly interrupted and the active electrode 202 may comprise two components (a portion outside the slot and a portion inside the slot). The width B of a slot is chosen so that essentially only gases can pass through the slots and tissues and liquids are too large to pass through the slots. In example systems, the width B of the slots may range from 0.001 to 0.003 inches (0.0254 to 0.0762 mm) (inclusive), and in a particular case 0.001 to 0.002 inches (0.0254 to 0.0508 mm). In some cases each slot has the same width B, in other cases different slots on the same active electrode may have different widths. Each slot has a fluid connection to the elastic tube member 116 and, below, various example systems of fluid connections are described.

If the primary passage 502 is not clogged during operation, probably few or no gas bubbles are drawn into the slots. That is, for the bubbles and liquids, the path of least resistance through the primary passage 502 and then through the corresponding passage in the spacer 200 leads. In periods, however, where the primary passage 502 is clogged completely or partially, a volume-controlled suction causes the application of a stronger vacuum by the peristaltic pump 118 , Increased vacuum periods (where the primary passage is completely or partially plugged) may cause the differential pressure in the slots to be sufficient to pull gas bubbles through the slots. Thus, in periods when bubbles tend to be increased and the field of view is obscured (ie, during total or partial obstruction of the primary passage), the slots tend to reduce visual impairment by removing gas bubbles from the field of view.

In some example systems, such as in 5 the spacer defines flow channels under the electrode 202 and essentially parallel to this. The flow channels are through a fluid connection with the elastic hose member 116 connected, in some cases by means of the main passage through the spacer 200 , The flow channels are in 6 shown below and are described in the appropriate text. In some cases, however, the flow channels define passages that follow the outer contour 218 adjacent to the active electrode. For example, shows 5 three such passages 510A . 510B and 510C , However, there may be one or more of the passages 510 to be used. With the passages 510 can gases and liquids near the outer outlines 218 be sucked from the active electrode, and so can also reduce the occlusion of the field of view.

6 shows an exploded view of the active electrode 202 and the spacer in these embodiments. In particular shows 6 the spacer 200 under the active electrode 202 , However, when it is mounted, it is adjacent to the spacer 200 at. That is, the spacer 200 defines a flat surface in these cases 600 , An inner surface 602 the active electrode (in contrast to the outer surface 204 ) also defines a plane, and when the active electrode is mounted, the inner surface is adjacent 602 the active electrode 202 to the plane surface 600 , The active electrode 202 can with any suitable mechanism with the spacer 200 get connected. In one case, the active electrode 202 using the passages 604A -D mechanically and electrically connected. That is, at least one of the passages 604 may comprise an electrical conductor passing through the passageway to the active electrode 202 is electrically connected, and the electrical conductor may at least partially the active electrode 202 mechanically at the spacer 200 Fasten. Likewise, additional mechanical elements of the active electrode 202 into the passages 604 of the spacer 200 lead and be attached, z. B. with epoxy adhesive. The active electrode may have additional passages and features for electrical and mechanical connection with the spacer 200 exhibit. However, these are not shown in order not to unnecessarily increase the complexity of the figure.

The spacer 200 also defines a primary passage 208 that has a functional relationship to the primary passage 502 the active electrode 202 having. Although in 6 not shown, defines the passage in some example systems 208 in the distance piece 200 a cross-section with the distance along the Absaugpfads to the proximal end 110 of the pen increases. The example distance piece 200 also includes several flow channels 606A -C. When the active electrode 202 to the spacer 200 adjacent, the individual flow channels 606A . 606B and 606C at least partially under the slot 504D . 504E respectively. 504F be positioned. There are three slots mapped to the flow channels, however, flow channels can be assigned any number of slots, including all slots, and thus can be located in the spacer 200 a larger or smaller number of flow channels to be defined. In periods of gas bubbles through the slots 504D -F, which are associated with flow channels, the flow path for the gas bubbles comprises the corresponding flow channels 606A -C as well as the primary passage 208 in the distance piece 200 , In the slots, which are not assigned to flow channels (eg 504B and 504C ), involves the flow path of the gas bubbles during periods in which these pass through the slots 504A -C between the active electrode 202 and the spacer 200 defined area as well as the primary passage 208 in the distance piece 200 ,

In some cases, each flow channel defines a depth T (measured from the plane surface 600 to the bottom of the channel at the distal end of the channel) from 0.007 to 0.008 inches (0.1778 to 0.2032 mm) (inclusive) and a width B (also measured from the distal end of the channel) from 0.007 to 0.008 inches (0 , 1778 to 0.2032 mm). However, other dimensions can be used. Consistent with the philosophy of increasing cross-section, the flow channels may have a distal cross-section (eg, below the corresponding slot) and a proximal cross-section (eg, closer to the primary passage 208 ), wherein the distal cross section is smaller than the proximal cross section.

As in 6 In some cases, the flow channels extend 606 to the outer outline 218 the active electrode 200 , and so define the distal ends of the flow channels, the passages 510 , In other cases, however, the flow channels can only so far in the direction of the outer contour 218 extend as needed to make them under the appropriate slots 504 are located. Therefore, the presence of a flow channel makes 606 in the distance piece 200 not required passages 510 available. In the example in 5 extends the flow channel 650 to the outside, so that he is under the slot 504B is, but not to the outer outline 218 the active electrode 202 , The flow channel 650 defines a constant cross-section along the flow channel to the primary passage, since the likelihood is relatively low that tissue only through the corresponding slots 504 enters the flow channels, and the risk of clogging is therefore low.

While the sample flow channels 606 and 650 via a direct fluid connection to the primary passage 208 the flow channels do not necessarily have to be that way. For example, the spacer may define passages, some or all of the slots 504 associated with the passages substantially parallel to the primary passage 208 run and finally via a fluid connection with the Absaugpfad in the elongated shaft 106 feature. 6 also shows examples of the slots 504 with the corresponding flow channels 606 (ie the slots 504B and 504D -F) and slots 504 without flow channels (ie the slots 504A and 504C ) to describe example situations. However, pens with slots and no flow channels and pins are contemplated in which each slot is associated with a flow channel. If flow channels are used, any number of flow channels that are to the outer contour 218 the active electrode 202 extend (any number between zero flow channels and all flow channels). Finally, any combination of slots and spacers can be used which provides a functional advantage. Slotted slot active electrodes may provide more functions when no standoffs are used, but slots and standoffs are not mutually exclusive.

7 shows a block diagram of a control unit 104 according to at least some embodiments. In particular, the control unit contains 104 a processor 700 , At the processor 700 it can be a microcontroller. Therefore, the microcontroller can be integrated with the read-only memory (ROM) 702 , the random access memory (RAM) 704 , the digital-to-analog converter (D / A) 706 , the analog-to-digital converter (A / D) 714 , the digital outputs (D / O) 708 and the digital inputs (D / I) 710 be. The processor 700 can also be integral with the communication logic 712 be to the communication of the processor 700 with external devices and internal devices such. B. the display 130 to enable. The processor 700 Although in some embodiments it may be implemented as a microcontroller, in other embodiments it may be implemented as a stand-alone main processor in combination with individual RAM, ROM, communication, A / D, D / A, D / O, and D / I devices, as well be implemented with communication hardware for communication with peripheral components.

In the ROM 702 Instructions are stored by the processor 700 can be executed. In particular, the ROM 702 include a software program, the execution of which causes the control unit to deliver RF energy to the active electrode and control the speed of the peristaltic pump. The RAM 704 can be used as memory for the processor 700 in which data is temporarily stored and instructions are executed. The processor 700 is using the digital-to-analog converter 706 (eg, in some embodiments, the RF voltage generator 716 ), the digital outputs 708 (eg, in some embodiments, the RF voltage generator 716 ), the digital inputs 710 (eg, interface devices such as the buttons 132 or the foot pedal group 134 ( 1 )) and the communication device 712 (eg the display 130 ) with other devices in the control unit 104 connected.

The voltage generator 716 generates an AC voltage signal with the active electrode 202 of the pen 102 connected is. In some embodiments, the voltage generator defines an active connection 718 that with the electrical contact 720 in the control unit connector 120 , the electrical contact 722 in the pin connector 114 and finally with the active electrode 202 connected is. Accordingly, the voltage generator defines a mating connection 724 that with the electrical contact 726 in the control unit connector 120 , the electrical contact 728 in the pin connector 114 and finally with the counter electrode (in some cases an elongated metal shaft 106 ) connected is. Additional active connections and / or mating connections can be used. At the active connection 718 are the voltages and electrical currents through the voltage generator 716 induced, and the mating terminal 724 provides a return for electrical currents. The counterpart connection 724 can provide a ground connection with the grounding for the control unit 104 is identical (eg grounding 730 for the keys 132 ). However, in other embodiments, the voltage generator is 716 not earthed (with the control unit 104 ), so the counterpart connection 724 has a voltage when it is grounded (eg grounding 730 ) is measured. A voltage generator 716 without earthing and thus the possibility of voltage readings at the counter connections 724 relative to grounding, however, does not conflict with the status of the connection 724 as a counter connection of the active connection 718 ,

The AC voltage signal from the voltage generator 716 generated and between the active connection 718 and the counterpart connection 724 RF energy, the frequency of which, in some embodiments, is between about 5 kilohertz (kHz) and 20 megahertz (MHz), in some cases between 30 kHz and 2.5 MHz, in other cases between 50 kHz and 500 kHz, often less than 350 kHz and often between 100 kHz and 200 kHz. In some applications, a frequency of about 100 kHz is useful because the impedance of the target tissue is much higher than 100 kHz.

The voltage generator 716 RMS voltage can range from about 5 volts (V) to 1800 volts, in some cases in the range of about 10 V to 500 V, often between about 10 V to 400 V, depending on the ablation mode and the Size of the active electrode. In some embodiments, that is from the voltage generator 716 For example, the peak voltage generated for ablation is a square wave voltage with a peak voltage in the range of 10V to 2000V, in some cases in the range of 100V to 1800V, in other cases in the range of about 28V to 1200V, and often in the range of approx 100V to 320V peak voltage.

The voltage and the current coming from the voltage generator 716 can be output in rows of voltage pulses or AC voltage at a sufficiently high frequency (eg, on the order of 5 kHz to 20 MHz) so that the voltage is effectively applied continuously (as compared, for example, with laser for low depth necrosis pulsed at about 10 Hz to 20 Hz). In addition, the duty cycle (ie the total time, in any second interval in which energy is applied) is one from the voltage generator 716 generated square wave voltage for some embodiments in the order of about 50% compared to laser, the duty cycle is about 0.0001%. Although square-wave voltages are generated and provided in some embodiments, the AC voltage signal may be modified to accommodate e.g. For example, to include features such as spikes in the leading or trailing edge of each halfwave, or the AC voltage signal is modifiable to assume particular shapes (eg, sine, triangle).

In 7 contains the control unit 104 according to various embodiments also the peristaltic pump 118 , The peristaltic pump 118 can be at least partially in the case 122 are located. The peristaltic pump includes the anchor 124 that with a shaft of the engine 734 mechanically connected. In some cases, the armature of the motor can be directly connected to the armature as shown in the figure 124 However, in other cases, different gears, discs and / or belts may be between the engine 734 and the anchor 124 are located. The motor 734 may have any suitable shape and z. As an AC motor, a DC motor and / or a stepping motor. For controlling the speed of the shaft of the motor 734 and thus for controlling the rotational speed of the armature 124 (and the volume flow of the pin), the engine 734 with an engine speed control circuit 736 get connected. In the illustrative case of an AC motor, the engine speed control circuit may 736 Control the voltage and frequency that are on the electric motor 734 be applied. In the case of a DC motor, the engine speed control circuit may be 736 the on the engine 734 control applied DC voltage. In the case of a stepping motor, the motor speed control circuit may be 736 control the current flowing to the poles of the motor, however, the stepper motor may have a sufficient number of poles or it is controlled so that the armature 124 turns evenly.

The processor 700 is with the engine speed control circuit 736 connected, z. B. via the digital-to-analog converter 706 (in the figure circle A). The processor 700 can also be connected in other ways, eg. B. as a packet-based communication connection via the communication port 712 , So can the processor 700 . executing a program that is active on the port 718 determine RF energy provided and, in response, make speed control changes (and thus changes in volumetric flow) by sending speed commands to the engine speed control circuit 736 sends. The engine speed control circuit 736 in turn implements the speed control changes. Speed control changes can possibly change the speed of the armature 124 , if necessary stopping the anchor 124 and in some ablation modes, the transient direction reversal of the anchor 124 include.

8th shows a method according to at least some embodiments. In particular, the procedure is started (block 800 ) and performs the following operations: generating plasma at an active electrode located at the distal end of an electrosurgical rod (block 802 ); Drawing liquid through a primary passage in the active electrode (block 804 ); Drawing the liquid through a first portion of a first passage in a spacer (block 806 ), wherein the liquid flows in the first portion at a first speed and the spacer is arranged at the distal end of the electrosurgical pencil; Drawing the liquid through a second section of the first flow in the spacer (block 808 ), wherein the liquid flows in the second section at a second speed, which is lower than the first speed. Then the procedure is terminated (block 810 ).

9 shows a method according to at least some embodiments. In particular, the procedure is started (block 900 ) and performs the following operations: generating plasma at an active electrode located at the distal end of an electrosurgical rod (block 902 ); Drawing liquid through a first slot defined by the active electrode (block 904 ), wherein the first slot is located closer to the outer contour of the active electrode than the primary passage; Drawing the liquid through a first flow channel defined in the spacer below the first slot (block 906 ). Then the procedure is terminated (block 908 ).

While preferred embodiments of this disclosure have been illustrated and described, modifications can be made to them by one skilled in the art without departing from the scope or spirit thereof. The embodiments described in this document are merely examples and should not be construed as limiting. Because many varying and different embodiments are possible within the scope of this inventive concept, including equivalent structures, materials, or methods which are subsequently contemplated, and as many modifications may be made to the embodiments described herein in accordance with legal requirements, it is to be understood that those herein described details are to be considered as illustrative and not restrictive.

QUOTES INCLUDE IN THE DESCRIPTION

This list of the documents listed by the applicant has been generated automatically and is included solely for the better information of the reader. The list is not part of the German patent or utility model application. The DPMA assumes no liability for any errors or omissions.

Cited patent literature

• US Pat. No. 5,697,882 [0031]

Cited non-patent literature

• "Introduction to Plasma Physics" by RJ Goldston and PH Rutherford of the Plasma Physics Laboratory of Princeton University (1995) [0029]

Claims (30)

An electrosurgical pencil, comprising: an elongated housing defining a handle end and a distal end; a hose member connected to the elongated housing; a spacer of non-conductive material disposed at the distal end; a conductive electrode disposed on the spacer defining an outer periphery; a first passage at least partially defined by the spacer, wherein the first passage has a fluid connection to the hose member; wherein the first passage defines a distal cross-section; and wherein the first passage defines a proximal cross-section that is closer to the handle end than the distal cross-section along a flow path, and wherein the distal cross-section is smaller than the proximal cross-section. An electrosurgical pencil according to claim 1, further comprising: a primary passage through the conductive electrode, the primary passage at the first passage being aligned through the spacer; and a first slot defined by the conductive electrode, wherein the first slot is located closer to the outer contour than the primary passage; wherein the width of the first slot is 0.0762 millimeters (mm) or less. The electrosurgical pencil of claim 2, wherein the first slot has a width of between 0.0254mm and 0.0508mm (inclusive). An electrosurgical pencil according to claim 2 or 3, further comprising: a second slot defined by the conductive electrode, the second slot being located closer to the outer periphery than the primary passage, the second slot being defined on a side of the primary passage opposite the first slot; wherein the width of the second slot is 0.0762 millimeters (mm) or less. The electrosurgical pencil of claim 4, further comprising a first flow channel defined in the spacer, wherein at least a portion of the flow channel is disposed below the first slot, the first flow channel defining a cross-section and the first flow channel having a fluid connection to the first passage. An electrosurgical pencil according to claim 5, wherein no flow channel is disposed below the second slot. An electrosurgical pencil according to any one of claims 2 to 6, wherein the first slot completely surrounds the primary passage. An electrosurgical pencil according to any one of claims 2 to 7, wherein the first slot is disposed parallel to the outer periphery. The electrosurgical pencil of any one of claims 2 to 8, further comprising a first flow channel defined in the spacer, wherein at least a portion of the flow channel is disposed below the first slot, and the first flow channel has fluid communication with the first passage. An electrosurgical pencil according to claim 9, further comprising: wherein the first flow channel defines a distal cross section; and wherein the first flow channel defines a proximal cross section, wherein the proximal cross section of the first flow channel along a flow path is closer to the handle end than the distal cross section of the first flow channel, and wherein the distal cross section of the first flow channel is smaller than the proximal cross section of the first flow channel. An electrosurgical pencil according to claim 9 or 10, wherein the first flow channel defines a passage adjacent to the outer periphery of the conductive electrode. An electrosurgical pencil according to any one of the preceding claims, comprising: a primary passage through the conductive electrode, wherein the primary passage is aligned with the first passage and the primary passage has fluid communication with the hose member; wherein the distal cross-section is measured perpendicular to a central axis of the first passage. The electrosurgical pencil of claim 12, wherein a largest dimension of the first passage is greater than the largest dimension of the primary passage. The electrosurgical wand of claim 12 or 13, wherein the largest dimension of the primary passageway through the conductive electrode is between one percent (1%) and twenty percent (20%) less than the largest dimension of the first passageway. An electrosurgical pencil according to claim 12, 13 or 14, wherein the largest dimension of the primary passage through the conductive electrode is at least fifteen percent (15%) is smaller than the largest dimension of the first passage. An electrosurgical pencil according to any one of claims 12 to 15, further comprising: a primary passage through the conductive electrode, wherein the primary passage is aligned with the first passage, and wherein the primary passage has fluid communication with the hose member; wherein the first passage is circular. The electrosurgical pencil of claim 16, wherein the diameter of the first passage is at least 1.0 millimeter. An electrosurgical pencil according to any one of the preceding claims, wherein the distal cross-section is between one percent (1%) and twenty percent (30%) smaller than the proximal cross-section. An electrosurgical pencil according to any one of the preceding claims, wherein the distal cross-section is at least twenty percent (20%) smaller than the proximal cross-section. An electrosurgical pencil, comprising: a fluid conduit configured to aspirate fluid from a distal end of the pen; a nonconductive spacer coupled to the distal end; an active electrode carried by the spacer and a suction opening, wherein the suction opening is narrower than the liquid line. The electrosurgical pencil of claim 20, wherein the spacer comprises at least one standoff pin, and wherein the standoff pin is configured such that the standoff pin projects beyond the active electrode at the distal end of the stud. An electrosurgical pencil according to claim 20 or 21, further comprising a pilot electrode. The electrosurgical pencil of claim 22, wherein the pilot electrode is recessed from the distal end of the stylus and the active electrode. An electrosurgical pencil according to claim 22 or 23, wherein the pilot electrode is smaller than the active electrode. An electrosurgical pencil device according to any one of claims 22, 23 or 24, and a controller configured to activate the pilot electrode to generate a plasma around at least a portion of the active electrode and then to activate the active electrode to provide the plasma expand plasma generated by the pilot electrode. The device of any of claims 22 to 25, wherein the pilot electrode is recessed in the spacer to prevent bubbles and / or plasma generated by the pilot electrode from being quenched by fluid flow across the distal end of the stylus. Device according to one of claims 20 to 26, wherein the spacer and / or the electrode at least one slot having a shape and / or size, which are selected so as to the flow of gas and / or plasma instead of liquid through the at least one Slot to enable. The device of claim 27, wherein the spacer and the electrode have at least one partially overlapping slot. Device according to one of claims 20 to 28 with a counter electrode. Device according to one of claims 20 to 28 having the features according to one of claims 1 to 19.

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