US20070213704A1 - Electrical discharge devices and techniques for medical procedures - Google Patents

Abstract

A medical instrument coupled to first and second energy means and a computer controller for the controlled volumetric removal of thin tissue layers. The system provides a source for introducing a gas to controllably form and capture transient gas volumes in a microchannel structure at the working surface of the instrument that interfaces with a targeted tissue site. Each of the microchannel features of the working surface carries an electrode element coupled to the electrical source. The energy may be applied to the targeted site in either of two modes of operation, depending in part on voltage and repetition rate of energy delivery. In one mode of energy application, electrical potential is selected to cause an intense electrical arc across the transient ionized gas volumes to cause an energy-tissue interaction characterized by tissue vaporization. In another preferred mode of energy delivery, the system applies selected levels of energy to the targeted site by means of an energetic plasma at the instrument working surface to cause molecular volatilization of surface macromolecules thus resulting in material removal. Both modes of operation limit collateral thermal damage to tissue volumes adjacent to the targeted site. Another preferred embodiment provides and an ultrasound source or other vibrational source coupled to the working end to cause cavitation in fluid about the working end.

Description

CROSS-REFERENCES TO RELATED APPLICATIONS
• This application is a continuation of U.S. patent application Ser. No. 11/065,180 (Attorney Docket No. 022356-000310US), filed Feb. 23, 2005, which was a continuation of Ser. No. 10/282,555 (Attorney Docket No. 022356-000300US), filed Oct. 28, 2002, which was a continuation-in-part of U.S. patent application Ser. No. 09/614,163, filed Jul. 11, 2000, titledElectrical Discharge Devices and Techniques for Plasma-Assisted Skin Resurfacing,which was a continuation-in-part of U.S. patent application Ser. No. 09/317,768, filed May 24, 1999, titledPhotoionized Gas Enabled Electrical Discharge Technique for Plasma-Mediated Cold Tissue Ablation,the full disclosures which are incorporated herein by reference.
BACKGROUND OF THE INVENTION
• 1. Field of the Invention
• The invention is related to electrosurgical instruments and techniques for precision application of energy to tissue, and more particularly to a system for thin layer ablation. More in particular, the working surface of a probe carries (i) delivery means for introducing and capturing a gas volume in a microchannel structure at an interface between the probe and the targeted site, (ii) energy delivery means for creating an intense electrical field of micron-dimensioned gas volumes to controllably apply intense energy to the targeted site to cause volumetric tissue removal, and (iii) vibration means for assisting in the creation of micron-scale gas volumes or bubbles.
• 2. Description of the Background Art
• Various electromagnetic and acoustic energy delivery sources have been investigated for surgical tissue ablation or removal, including radiofrequency (Rf) current flow within tissue, high intensity focused ultrasound (HFU) tissue interactions and microwave energy absorption in tissue. In general, at high intensities, the above listed energy sources generate thermal effects that can vaporize tissue as the means of tissue ablation or removal. In other words, the energy sources elevate the temperature of water in intra- and extracellular spaces to above 100° C. thereby explosively vaporizing water to damage or destroy the tissue. The drawback to such purely thermally-mediated ablations is significant collateral damage to tissue volumes adjacent to the targeted site. While in many surgical fields, the above-described collateral thermal damage may be acceptable, in fields such where thin layer ablations are required, such as skin resurfacing, ophthalmology, neurology, and interventional cardiology, there is a need to prevent, or limit, any such collateral damage.
• Lasers for Use in Tissue Ablation. Various laser systems have been developed for tissue ablation. The conventional long-pulse laser systems outside the UV range, wherein long-pulse is defined as a system operating in a range of 10's of nanoseconds to microseconds in pulse duration, have been found to be inefficient in volumetric tissue removal without causing extensive collateral damage. In a the conventional long-pulse laser system (e.g., Nd:YAG, Er:YAG, IR lasers), the photonic energy delivered to a targeted site does not directly disrupt the molecular integrity of surface layers of the site, but rather the energy is transferred into surrounding tissue volumes as photothermal energy, or photomechanical energy. These collateral effects propagate through surrounding tissues as heat, and perhaps mechanical shock waves, which manifest themselves as undesirable collateral damage. More specifically, the generally accepted model of volumetric ablation or removal with lasers having a pulse longer than tens or hundreds of picoseconds is described as follows: The energy absorption is chromophore dependent (and/or scattering dependent), and the energy transfer involves the heating of conduction band electrons by the incident beam of coherent photons which is followed by transfer of thermal energy to the structure's lattice. Ablation or damage occurs by conventional heat deposition resulting in vaporization, melting, or fracture of the structure. The rate of volumetric structure removal depends on thermal conduction through the structure lattice and its thermodynamic properties (heat capacity, heat of vaporization, heat of fusion, etc.). Thus, the minimum energy requirements to cause an ablation effect in the structure's properties may be defined by a threshold of incident laser energy per unit of structure volume at the target site, which threshold is directly dependent on pulse duration. It has been found that ablation thresholds generally require relatively long pulse durations, which in turn are the source of undesirable collateral photothermal (or photomechanical) damage.
• In certain tissue ablation fields (e.g., corneal ablation in ophthalmology), excimer lasers have been developed that emit high intensity pulses of ultraviolet (UV) light, typically with pulse durations in the 1 ns to 100 ns range. The short wavelengths, as well as sequenced nanosecond pulse regimes, define a substantially non-thermally mediated form of tissue ablation. Short wavelength UV photons are highly energetic and when radiated onto biological tissue can directly break the chemical bonds in surface layer molecules of the tissue. As a consequence, UV excimer lasers can vaporize or breakdown a surface tissue layer with minimal thermal energy transfer to underlying (or adjacent) tissue volumes. The by-product of the breakdown is predominantly a gas that is ejected away from the surface on which the energy was deposited, thus generally leaving the subsurface layer free from substantial collateral thermal damage. Tissue ablation with UV irradiation with can be controlled depth-wise since biological tissues exhibit strong absorption in the UV region of the electromagnetic spectrum (e.g., at c. 1.93 μm). In biological tissue, UV radiation typically only penetrates to a depth of from about 0.25 μm to about 4.0 μm per pulse in the ns duration pulses described above. Thus, to ablate to a certain depth, the system uses a pre-determined number of pulses of ns energy delivery
• While UV photonic energy delivery can reduce collateral damage in tissue ablation, there are numerous disadvantages that limit the applicability of UV lasers to biomedical procedures. First, UV photonic energy delivery cannot be easily delivered to a targeted site of a body structure in a fluid environment (e.g., thrombus in a blood vessel) since intervening fluid may absorb energy rather than the target site. For this reason, UV energy delivery is most useful for ablating tissue surfaces exposed to the atmosphere, such as a patient's cornea in a LASIK procedure. Second, the desired lack of collateral damage in UV ablation is known to occur when a single pulse of UV photonic energy irradiates a tissue surface. However, when the UV pulse repetition rate exceeds about 5 to 10 Hz, considerable photothermal collateral damage (as well as photomechanical collateral damage) has been observed. Thus, UV ablation generally may result in low volumetric removals of tissue surfaces per unit of time. Third, while UV photons carry sufficient energy to directly break chemical bonds in surface molecules of tissue, UV wavelengths also may be sufficiently energetic to promote mutagenic effects thus elevating concerns about the long-term health and health of the clinician and the patient.
• Conventional Electrosurgical Ablation of Tissue Volumes. Radiofrequency currents in tissue have been known for many years in the prior art for cutting a tissue mass, or for coagulating regions within a tissue mass. Conventional electrosurgical systems known in the art ablate tissue by applying an electrical field across the tissue to be treated. The actual energy-tissue interaction in Rf cutting is typically described in terms of a voltage differential that causes a spark or arc across a gap between anactive electrode2aand the targeted site (e.g., coupled to areturn electrode2b) as shown inFIG. 1A. In the prior art instrument ofFIG. 1A, a high energy density capable of tissue cutting is created when the gap between theactive electrode2aand the tissue surface is occupied with an electrically non-conductive gas, or an electrically insulative liquid.FIG. 1A depicts a typical ablation modality in whichelectrode2ais moved into contact with a liquid or moisture layer on an exposed tissue mass which vaporizes a plurality ofrandom bubbles3. The bubbles comprise insulative gas volumes and randomly can form a momentary insulative physical gap between theactive electrode2aand the tissue (coupled to returnelectrode2b) resulting in a spark across the gap. Such an Rf spark created between the active electrode and the tissue will cause localized damage and ablation at the discharge conduction site at the surface of the tissue. In other words, the spark causes very high energy densities at the random location that the tissue interfaces thebubble3 which in turn results in intense heat that disrupts and ablates a site on the tissue surface. InFIG. 1A, it can be seen thatconductive paths4 indicate the paths of current flow. The conventional electrosurgical ablation ofFIG. 1A generally is achieved at frequencies ranging from 500 kHz to 2.5 MHz, with power levels ranging from 75 to 750 W. In such prior art tissue cutting with Rf currents, the current density rapidly decreases with distance from the exact energy deposition site on the tissue which is contacted by the spark. Still, the depth of tissue disruption and damage in such prior art electrosurgical cutting may range from about 0.3 mm. to as much as 3.5 mm. (see R. D. Tucker et al,Histologic characteristics of electrosurgical injuries, Journal Am. Assoc. Gynecol. Laparoscopy4(2), pp. 201-206 1997.) The depth of tissue ablation depends on several variables, including (i) the conductivity of the tissue, (ii) the insulative characteristics of the media in the physical gap between the active electrode(s) and the tissue; (iii) the dimension of the physical gap between the electrode(s) and the tissue; (iv) the power setting and optional feedback control of the power level based upon electrical characteristics of the targeted tissue; (v) and the translation of the working end relative to the tissue.
• Electrosurgcal Ablation with the Coblator™ System. A recently commercialized invention in the field of electrosurgical ablation was invented by Eggers et al and is a called Coblator™ system (see. e.g., disclosures of Eggers et al in U.S. Pat. Nos. 5,873,855; 5,888,198; 5,891,095; 6,024,733; 6,032,674; 6,066,134 and the companion patents cited therein). The Coblator™ system relies on the creation of a voltage difference between a plurality of closely spaced rod-like electrode elements2aand areturn electrode2b(seeFIG. 1B) wherein the working end carries both the active and return electrodes. The Coblator™ system differs from conventional electrosurgical devices in that the system introduces an electrically conductive fluid such asisotonic saline5 into the physical gaps6 between the closely spaced active electrodes, and between the electrode group and the targeted tissue. The system applies electrical energy with a frequency of about 100 kHz and a voltage of about 100 to 300 V.
• The Coblator™ company promotional materials explain that at high voltage levels, the electricallyconductive fluid5 in the gaps6 that intervene between the closely spacedactive electrodes2ais converted into an ionized vapor or plasma. As evidence of the character of such a plasma, studies have shown that a typical plasma has an orange glow. Spectroscopic analysis of Coblator emissions show an emission peak of around 590 nm which is characteristic of the sodium ionization peak (NaCl normal solution used as conductive fluid), with negligible emissions above 600 nm. The company promotional material claims that conventional electrosurgical ablation yields a continuous spectrum from 490 nm to 900 nm, peaking at around 700 nm.
• The supposition underlying the Coblator™ is that the actual energy-tissue interaction produced by the system relates to charged particles in the plasma having sufficient energy to cause dissociation of molecular bonds within tissue structures that come into contact with the plasma. Based on this hypothesis, the accelerated charged particles have a very short range of travel, and the energy-tissue interaction is confined largely to thin surface layers. Further, the supposition is that the energy-tissue interaction is a “cold” process that does not rely on the thermal vaporization of intra- and extracellular fluids to ablate tissue. In this respect, the Coblator™ system has been described as producing an ablation that compares to that of an excimer laser, both of which produce similar ablation by-products—if relying on comparison of spectrographic emission peaks. The energy required to cause molecular break-down of common molecular bonds in tissue is believed to be in the range of 3.0 eV to 5.0 eV or more. Considering the amount of energy utilized by the Coblator™ system to initially and thereafter continually vaporize NaCl from within a saline solution, it raises the question whether the plasma volumes can sustainably provide the energy levels required for true molecular dissociation of compositions in tissue surfaces, as with an excimer laser.
• Another hypothesis that explains the Coblator™ ablation process in more mundane. Referring toFIG. 1B, it can be seen that the Coblator™ working end traps conductivefluid5 within the many gaps6 between the closely spaces electrode elements. As electrical potential is increased at theelectrodes2a,random and dynamic conductive paths are created to thereturn electrode2bfrom random discharge points on theactive electrodes2a.Such conductive paths essentially comprise a dynamic uncontrolled distribution of NaCl molecules in the fluid, that can be momentarily linked by high energy densities along the conductive path that will, in turn, vaporize such compositions. The result is a frothy environment of random expanding and collapsingbubbles3 as shown inFIG. 1B. Since the randomtransient bubbles5 may comprise a quasi-neutral gas or a substantially insulative gas—thereafter a spark or dischargepath4 can occur along some random routes between theactive electrode2aand thereturn electrode2band within thebubbles3. As shown inFIG. 1B, when such random insulative bubbles and anelectrical spark path4 occurs with the tissue surface being intermediate to the active and return electrodes, a spark-type energy-tissue interaction will occur that delivers ablative energy to the tissue at any random location that abubble3 in thepath4 interfaces the tissue. WhileFIG. 1B shows two random spark-type events through a frothy gas bubble environment, if this hypothesis were accepted, an actual Coblator™ ablation comprises 1000's of such random and discrete spark-type events per second to cause tissue ablation. According to this hypothesis, the Coblator™ system would produce an energy-tissue interaction much like that of conventional electrosurgical ablation as depicted inFIG. 1A.
• This hypothesis easily explains the two observations made by proponents of the Coblator™ that state (i) that spectroscopic analysis of energy delivery within a conductive fluid supports the theory of molecular dissociation, and (ii) that evidence of limited collateral thermal damage (so-called “cold” ablation) must be the result of a molecular dissociation process. First, the spectroscopic analysis of the Coblator™ ablation certainly would show emission peaks for vaporization of the sodium analytes in the fluid, which is a primary sink of the energy applied from the device—which is different from and predominates over any emission peaks from the tissue ablation. The tissue ablation, if the competing hypothesis of a spark-type interaction ofFIG. 1B is accurate, would be characterized by energy-to-tissue events that produce mostly water vapor from the vaporization of intra- and extracellular fluids. Such vapor would be rapidly absorbed by the surrounding fluid environment and might not contribute to any emissions that could be observed by spectrographic analysis of the bubbles of vaporized NaCl. Second,FIG. 1B depicts that the random discrete spark-type events that vaporize tissue are brief—occurring in a the very short, random time intervals in which the insulative bubbles are intact. The lifespan of a bubble is likely to have a duration ranging between 100's of ns to 10's of ms. As is well known, for a tissue ablation to be a substantially cold process, the intervals between successive thermal energy delivery events simply must be longer than the thermal relaxation time of the tissue which is dependent of several tissue characteristics. The thermal relaxation time also must take into consideration the boundary conditions. In the Coblator™ process as depicted inFIG. 1B, the thermal relaxation time of any typical tissue is probably in the range of 100's of ns. In addition, the fluid comprises a boundary condition that acts as a tremendous heat sink. Since the location of spark-type energy applications to tissue is random in location and brief in duration, the combination of (i) the thermal relaxation of the tissue, and (ii) the fluid heat sink removing heat from the tissue can easily return the ablated tissue location to a normal temperature before another random spark-type event occurs in a similar location. Thus, the hypothesis of molecular dissociation is not necessary to explain the “coolness” of the ablation depicted inFIG. 1B.
• The types of ablation caused by conventional electrosurgical ablation (seeFIG. 1A) and the type of ablation caused by the Coblator™ system (seeFIG. 1B—no matter the hypothesis selected to explain the Coblator™ energy-tissue-interaction—share several common characteristics. While conventional and the Coblator™ ablations are suitable for many procedures, both types of ablation are caused by totally random events wherein high electrical energy densities vaporize a fluid or elements therein to create an insulative gas or plasma volume that thereafter causes random localization of an energy-tissue interaction that ablates tissue. By the term random localization, it is meant that while the general location of tissue ablation is known for any time interval, the exact location of an ablation event, for example for any interval in the ns range, is unpredictable. As a further explanation,FIG. 2 represents an enlarged view of a portion of the Coblator™ working end ofFIG. 1B with a grid in perspective view as the tissue surface. The location at which the gas volume, or plasma, interfaces the tissue surface is random and the application of energy to the surface will be of very low resolution. If each grid ofFIG. 2 is between 10 to 20 μm, the lateral distance d between the point of energy emission and the point of highest energy density (herein called the energy deposition or application site) wherein the energy-tissue interaction is localized may as much as 100 to 500 μm from a reference axis x of the working end, or the lateral distance d could be zero. A further graphically depiction of what is meant by the concept of random localization of energy-tissue interactions is shown inFIG. 2. In that Figure, the energy delivery horizon (or perimeter) is indicated at h, by which is meant that, at a ns or ms time-scale, the actual application of energy to the tissue may be localized anywhere in the delivery horizon h, and the location of any such application will be entirely random within this horizon.
• Another characteristic common to both conventional electrosurgical ablation (FIG. 1A) and the Coblator™ ablation (FIG. 1B) relates to (i) the random size of and energy contact site and (ii) the random distribution of energy across the localized site of energy contact.FIG. 2 graphically depicts a random energy contact and ejecta e from such energy application being irregularly distributed across the energy deposition site. Since the actual energy application occurs only in a dynamic, frothy, expanding and collapsing vapor bubble environment, it is believed thatFIG. 2 somewhat accurately depicts the typical energy distribution. In any event, on a ns or ms time-scale, it is clear that the dimensions and energy distribution characteristics of energy delivery are uncontrolled and random. This is to be contrasted with lasers energy delivery systems in which localization can be precise with a few μm's and energy distribution across the site can be designed as Gaussian (higher energy in center of site) or “top-hat” (even energy distribution across the energy deposition site).
• While conventional electrosurgical ablation and Coblator™ type ablations are suitable for various procedures, the following characteristics common to both types of ablation prevent the possibility of more precise ablations with such prior art systems:
• (i) the actual energy deposition site is randomly localized instead of precisely localized;
• (ii) the energy density across the energy deposition site is random and uncontrolled;
• (iii) the conductive path between and energy deposition site and the emission point on an electrode is random;
• (iv) the dimensions of the energy deposition site are random and uncontrolled;
• (v) the amount of energy applied per unit of surface at an energy deposition site is random;
• (vi) the amount of energy applied per time interval at an energy deposition site is uncontrolled;
• (vii) the duration of intervals between successive energy applications to a site are random;
• (viii) the actual duration of an interval of energy application is random and uncontrolled;
• (ix) the conductive or insulative characteristics of media between the active electrode and the targeted site, at a micro-scale, are uncontrolled,
• (xi) the dimensions, localization, distribution and duration of insulative gas volumes or plasma volumes that facilitate energy delivery are random and uncontrolled; and
• (xii) the prior art instrument working ends function dramatically differently depending on the axial distance between an electrode surface and the targeted tissue surface,
• It would be highly desirable to have greater precision in thin layer ablations for microsurgeries, neurology, and precision skin resurfacing for burn debridement or cosmetic purposes. What is needed are systems and methods for selective volumetric removal of body surface layer portions (i) that are precisely controllable; (ii) that do not rely on thermal vaporization effects to ablate tissue; (iii) that can be activated in a controlled mode that ratably removes depths or volume of tissue in a given time interval to provide selective tissue decomposition; (iv) that allow for well-defined post treatment boundaries between layers of tissue decomposition and undamaged layers; (v) that removes surface structure that is exposed to a gas environment or immersed in a fluid environment; (vi) that provide for energy delivery to a patient's body structure via a working end that can be reduced in scale to less than 1 mm. to 3 mm. in diameter for micro-interventional use; and (vii) that utilize a working end that is simple to manufacture and therefore inexpensive and disposable.
BRIEF SUMMARY OF THE INVENTION
• The principal objective of the present invention is to provide controlled and precise applications of energy to a thin surface layer of structure in a patient's body to cause volumetric removal of layer portions substantially without collateral thermal damage. More in particular, an instrument working end is adapted (i) to deliver high intensity electrical energy in a preferred modality to create a highly energetic and dynamic microplasmas for causing molecular volatilization of surface macromolecules to remove tissue with microscale precision, or (ii) to optionally deliver a spark-type energytissue interaction (herein termed a conventional electrosurgical ablation modality) but in a novel micro-scale modality to controllably ablate discrete tissue portions.
• The novel energy delivery modalities and energy-tissue interactions are based on utilizing either of two novel principles (hereafter defined at times as control principles) in the application of electrical energy to body structures for ablation purposes. The principles may be applied to a system and instrument working surface independently, or preferably in tandem, and are designed to control the numerous factors that to date have been uncontrolled and random in tissue ablations (i.e., the 12 factors listed above at the end of the Section titled Description of the Related Art.
• The first control principle relates to bifurcation of a discrete electrical energy delivery event into two components. (i) the provision of electrical potential at an electrode at an intensity level that can ablate tissue with the electrode spaced apart from the targeted site; and (ii) the ms or ns (microsecond or nanosecond) control of conductive the characteristics, or ionization, of selected media in the interface between the electrode and the targeted site. In other words, it is postulated that the selected media can be switched between non-conductive (or insulative) and conductive (or ionized) stated in a controlled and ultrafast manner to advantageously deliver energy to cause a novel energy-tissue interaction. In a subset of this principle, several ionization methods, as well as energy-enhancing means for energizing a plasma, are disclosed-with photoionization being a preferred means.
• The second control principle relates to a tremendous reduction in scale, or micronization, of the features of the working surface for the purpose of controllably localizing a large number of discrete energy-tissue interactions, as well as controlling the physical dimensions of plasma volumes. As will be described below, the working surface may be fabricated by semiconductor processing techniques to provide features in the 5 μm to 10 μm range, by which is meant that widely dispersed micron-scale electrode elements may each apply electrical energy to a localized site to provide discrete spaced apart ablation events. Referring toFIG. 4, it is believed that the system and method of the invention can provide the type of resolution of energy application represented inFIG. 4, which depicts a controlled, discrete, localized energy-tissue interaction eti having a micro-scale dimension (FIG. 4 representing a perspective view of a 5 μm to 10 μm grid).
• The system is coupled to a computer controller for controlling intervals of energy delivery-both the ionization means and the electrical energy means for the ablation-as well as for optional flows of the selected media. By controlling the duration of intervals of energy applications and the repetition rate in relation to the thermal relaxation time of the targeted surface, it is postulated that the disclosed plasma-assisted tissue removal method will be a substantially cold process, ie., there will be substantially no collateral thermal damage to tissue.
• Each pulse, or burst, of energy application in the disclosed ablation process is assisted or enabled by a sequence of distinct plasma formation processes to achieve the operational objectives of the invention, followed by plasma decay intervals. In an initial portion of the process, an ionized gas (plasma) is formed to allow subsequent electrical potential in a spatially-controlled region at the surface layer. In a second portion of the process, an electrical discharge is created in the ionized gas and surface layer thus causing volatilization of macromolecules of the targeted surface layers to remove layer portions. To define the uses of plasmas herein, it is useful to provide the following background. A plasma is a quasineutral (partly ionized) gas having a significant proportion of charged particles relative to neutral particles which may, in an equilibrium state, exhibit collective behavior. Of interest to this invention are non-equilibrium or highly dynamic microplasmas formed proximate to structure in a patient's body to allow for energy transfer to, or deposition of energy within, thin surface layers of structure in a patient's body to remove (ablate) material without transfer of thermal energy. In the lexicon of physicists, a plasma may be defined simply as an ionized gas, to distinguish it from ordinary or neutral gases. In a neutral gas, each gas atom carries the same number of negatively charged electrons orbiting its nucleus as there are positively charged protons in that nucleus. While a neutral gas may carry the potential of substantial chemical activity together with dynamic effects (e.g., fluid turbulence), such a neutral gas exhibits little or no response to electric and magnetic fields—and such neutral gases are substantially unable to conduct electrical potential therethrough. A neutral gas, however, can be excited or energized to the plasma state when a sufficient proportion of its atoms become ionized by losing one or more electrons. Ionization can occur as a result of a number of processes, such as (i) a neutral gas becoming so hot as to cause the atoms to collide and jar loose electrons (thermal ionization or TI), (ii) a neutral gas being subjected to a high intensity light source that strikes the atoms with energetic photons that displace electrons from their orbits (photoionization or PI), (iii) a neutral gas being subjected to electric fields that are strong enough to strip away electrons from the atoms (field ionization of FI), and (iv) in the case of non-gaseous materials, a spark or electrical discharge pulse can ionize analytes in the surface of a solid.
• A resulting plasma (ionized gas) consists of interpenetrating and interacting accumulations of freely roaming charges (both negative and positive). This gas state can shift from neutral to ionized by photoionization or field ionization by the means disclosed herein, it is believed, within the range of tens of femtoseconds to hundreds of picoseconds. For purposes of this disclosure, the method of forming the initial plasma (ionized gas) volume involves irradiating a captured neutral gas volume with a high intensity wavelength (λ) ranging between about 190 nm to 263 nm (or more broadly, within the UV spectrum defined as λ from 10 nm to 400 nm; or, frequency range of 1.0×10¹⁵Hz to 6.0×10¹⁶Hz). Thereafter, an intense application of energy is applied by to targeted surface layer by creating an ultrafast high-intensity electrical discharge within the ionized gas volume and the surface layer to cause an electrochemical volatilization of molecules of the surface layer, i.e., a plasma-mediated ablation. Each high intensity burst of electrical energy forms a critical density plasma at the surface layer thus removing surface material that is ionized. According to this plasma-mediated form of electrochemical material removal, each energy pulse applied to the surface layer when above a certain threshold level is channeled into to the formation of ejecta (gas plume and fragments) by the volatilization or decomposition of macromolecules of the surface layer. The plasma, or microplasma, decays rapidly as ejecta and the plasma transfers heat and energy away from the surface layer and also releases energy in the form of radiative emissions. It is postulated that such energy applications to the surface layer (dependent on ionization proportion of neutral gas and intensity of the electrical discharge), can be modeled to provide selective volumetric removal of material per pulse of energy. In sum, a controllable process for selective volumetric tissue removal is provided by a system including a computer controller for successively rapid sequencing of (ii) photoionization of a partially-captured neutral gas volume, and (ii) creation of a high-intensity electrical field for volatilization of a targeted thin surface layer.
• In the present invention, at sufficiently high energy levels (or voltage V), charged particles in a plasma can possess sufficient energy to break down common molecular bonds in macromolecules of a tissue surface. For example, such bonds may be carbon-carbon bonds, carbon-nitrogen bonds, etc. It is believed that the energy required to disrupt such bonds is within the range of 3.0 eV to 4.0 eV. Preliminary calculations (to be refined for publication in a future disclosure) suggest that the estimated electron energy applied by the inventive system can far exceed 4.0 eV when operating at 300 to 1000 volts, making various assumptions concerning distances between the active electrode(s) and the targeted site; and the electron population of the media (gas or liquid) interface between the electrode(s) and the targeted site.
• The invention provides a technique for biological material removal that allows precision of ablation depth by removing a discrete thin layer of material with optional modes of (i) pulsed applications of intense energy to a targeted site, or (ii) the creation of a sustainable high energy plasma at the interface between a working surface and the targeted site to cause molecular volatilization.
• The invention advantageously provides a control technique for controlling material removal by causing a plurality of micron-dimensioned energy-tissue interactions over a grid of an instrument working surface.
• The invention advantageously provides a control technique for controlling material removal by creating a plurality of micron-dimensioned gas volumes that can be switched between non-conductive and conductive states for controlling energy applications to the targeted tissue surface.
• The invention provides a control technique for controlling the distribution of energy across a targeted site by creating a plurality of micron-dimensioned plasma volumes that evenly apply energy across tissue.
• The invention provides a control technique for enhancing the energy of a plasma to facilitate a plasma-mediated ablation by utilizing electron-emissive coatings and UV irradiation of a microchannel plate.
• The invention advantageously provides a technique for removal of surface layers of body structure substantially without collateral thermal damage.
• The invention advantageously provides a technique for ablation (material removal) that is generally insensitive to tissue's linear absorption characteristics.
• The invention advantageously provides a technique for ablation (material removal) that is generally insensitive to tissue hydration.
• The invention advantageously provides a technique for ablation of surface layers of body structure that is exposed to a gas environment or immersed in a fluid environment.
BRIEF DESCRIPTION OF THE DRAWINGS
• FIG. 1A is a view of a prior art working end of a monopolar probe in relation to a tissue surface illustrating the method of creating insulative gas bubble to cause spark-type discharges to ablate tissue.
• FIG. 1B is a view of a prior art working end of a bi-polar probe in relation to a tissue surface illustrating its the method of ablating tissue.
• FIG. 2 is a sectional view of a portion of the prior art working end ofFIG. 1B depicting the lack of localization of an energy application event.
• FIG. 3 is a micron-scaled grid representing a tissue surface that provides another view depicting the prior art lack of localization of an energy application event utilizing the prior art instruments of eitherFIG. 1A orFIG. 1B.
• FIG. 4 is a micron-scaled grid representing a tissue surface similar to that ofFIG. 3 that indicates the resolution of energy-tissue interactions that are possible with the present invention.
• FIG. 5 is a plan view of an exemplary probe of the invention in relation to a human hand and a simplified block schematic diagram of the energy sources of the system suitable for practice of the principles of the invention.
• FIG. 6 is an enlarged sectional view of the working end of the probe ofFIG. 5 taken along line6-6 ofFIG. 5.
• FIGS. 7A-7B are sectional schematic views of alternative shape structures at a working face of a probe similar to that shown inFIG. 6.
• FIGS. 8A-8B are views of a method of practicing the principles of the invention in a laminectomy/disketomy procedure for treating a herniated disc;FIG. 8A being a view of introducing the working end of the probe ofFIG. 5 into a workspace proximate to the patient's spine;FIG. 8B being an enlarged view of the working end in a portion of a fluid-filled workspace proximate to surface layers of a targeted structure.
• FIGS. 9A-9E are greatly enlarged views of the sequence of steps that comprise the method of practicing the principles of the invention for removing layers of any surface of a body structure immersed in a fluid;FIG. 9A being an illustration of the distal working face in the fluid environment;FIG. 9B depicting a neutral gas being introduced into shape structure of the working face displacing the immersion fluid;FIG. 9C depicting irradiation of the neutral gas volume with UV energy thereby photoionizing the gas in a first (estimated) ps time interval;FIG. 9D depicting an initial (estimated) ps time interval in creating a high-intensity electrical field in the ionized gas volume to create a plasma and thereby ablating tissue;FIG. 9E depicting a subsequent time interval wherein the sequence of events begin to be repeated as the neutral gas is introduced into the working face.
• FIG. 10 is a perspective view of the working end of an exemplary Type “C” system of the invention and its use in a skin resurfacing procedure.
• FIG. 11 is a sectional view of the working end ofFIG. 10 showing the microchannel structure of the working surface and a block schematic diagram of the energy sources of the system.
• FIG. 12 is a greatly enlarged sectional view of the working end ofFIG. 11 showing the microchannel structure of the working surface in more detail.
• FIG. 13 is an enlarged sectional view of a single microchannel similar toFIG. 12 showing an optional electronemissive coating added to the proximal region of the microchannel structure.
• FIG. 14A is a view of an exemplary micro-scale gas volume without the surrounding structure of the working surface that illustrates a surface engagement plane about the volume and the area that engages an electrode.
• FIG. 14B is another view of the exemplary micro-scale gas volume ofFIG. 14A shown in a relation to a microchannel with a surrounding gas environment also depicted graphically.
• FIGS. 15A-15E are views of a first mode of practicing the principles of the invention with the Type “C” system of FIGS.11-12:
• FIG. 15A is a view of a plurality of microchannel terminations with the surrounding structure of the working surface in phantom view in relation to a micron-dimensioned grid representing the targeted site, and further depicting the step of creating electrical potential at the electrodes;
• FIG. 15B is a view of the plurality of introduced media volumes similar toFIG. 14A after the step of ionization of the volumes by a UV source with the ionization graphically depicted as shading;
• FIG. 15C is a similar to that ofFIG. 15B this time depicting the transient (ionized) conductive path in the surrounding gas media that is extended distally from the working surface.
• FIG. 15D is similar toFIG. 15B and occurs substantially contemporaneous with the ionization ofFIG. 15B at which time the electrical potential at the electrode controllably applies energy across the ionized media volume to the targeted site.
• FIG. 15E followsFIG. 15D after a brief interval (estimated at 10's of ns) and depicts the material removal process (not-to-scale) wherein the application of energy cause volumetric material removal resulting in an ejecta plume into the remnants of the ionized gas media.
• FIG. 16A is a graphical view of a “top hat” energy distribution across a laser energy-tissue interaction.
• FIG. 16B is a graphical view of a Gaussian energy distribution across a laser energy-tissue interaction.
• FIG. 17 is a view of a second mode of practicing the principles of the invention with the Type “C” system by utilizing electron emissions from a microchannel plate (MCP) to energize the gas volumes depicted inFIG. 11 to achieve a plasma-mediated ablation.
• FIG. 18 is a view of an alternative embodiment of working end for practicing the method ofFIG. 17 in which multiple MCP's are arranged in a chevron pattern to further enhance an electron avalanche in plasma volumes.
• FIG. 19A is a view of the distal end of another probe member that carries a microchannel plate structure similar to that ofFIG. 11, this time utilizing field ionization of captured gas volumes, the working end adapted for thin layer ablation of mucosal layers.
• FIG. 19B is a sectional view of the distal end of the probe member ofFIG. 19A.
• FIG. 19C is a greatly enlarged sectional view of the working end of the probe member ofFIG. 19B showing the microchannel structure.
• FIG. 19D is a view of practicing the principles of the invention with the working end ofFIG. 19C using field ionization means to switch the gas volumes flowing through the microchannel structure between conductive and nonconductive states.
• FIG. 20 is a cut-away view of a working surface of an exemplary Type “D” system which is similar to the Type “C” system except for the use of multiple out-of-phase electrodes to insure continuous high voltage energy delivery to a plasma for plasma mediated ablations.
• FIG. 21 is a sectional view of a working surface similar to that ofFIG. 20 adapted for functioning without the neutral gas inflows through open-ended microchannels.
• FIG. 22A is a sectional view of a working surface of a Type “E” system with the addition of a vibration source coupled to thereto.
• FIG. 22B is another sectional view of the working surface ofFIG. 22A illustrating a method use.
• FIG. 23 is a sectional view of a working surface of another Type “E” system that uses ultrasonic energy to create cavitation that cooperates with electrical energy application to the targeted tissue.
DETAILED DESCRIPTION OF THE INVENTION
• I. Operational Principles of Plasma-Assisted Cold Ablation of Thin Surface Layers
• The several principles of operation of an exemplary plasma-mediated ablation system5 (seeFIG. 5) for the ratable removal of thin surface layers will be described in detail in the following sections in connection with an exemplary procedure: the selective removal of targeted tissue that is proximate to a delicate structure such as a nerve (e.g., material removal in a larninectomy/disketomy procedure for treating a herniated disc). The following description of the operation the probe ofFIGS. 5-6 and the techniques ofFIGS. 9A-9B and9A-9F are for exemplary purposes only and are not intended to limit the application of the system and methods of the invention. As will be described in further detail herein, the system may have application in a wide variety of surface layer ablations and volumetric tissue removal procedures. Thesystem5, which may be described herein as a PASCAL system (plasma-assisted cold ablation layer-by layer), is developed in accordance with the following operational principles, which will be described seriatim. The PASCAL system provides: (A) ultrafast pulses of energy applied to thin surface layers to create critical density microplasma events without transfer of thermal energy, (B) confinement means for at least partially confining a nonequilibrium microplasma formed by photoionization to allow electrical potential therein to thereby allow energy application by an electrical source (as opposed to laser source), (C) control means for controlling pulse duration and the repetition of energy application events to provide layer-by-layer volumetric material removal; and (D) feedback control systems (optional) based on analysis of plasma luminescence caused by the plasma-mediated ablation process.
• A. Operational Principle: Ultrafast Pulsed Energy Application for Volatilization of Surface Layers.
• A first objective of the present invention is to provide an ultrafast pulsed application of electrical energy to a targeted site on a surface layer of structure in a patient's body. In this invention, each discrete application of energy (pulse or burst) can be defined by quantity of energy (J) and a duration in which such energy is deposited within the surface layer. A first operational principal of the invention is that, for a given energy quantity in joules, the duration of energy application is less than a threshold electron-to-lattice energy transfer time for the surface layer of the targeted structure. It is postulated that for surface layers of structures here in question, this characteristic energy transfer time is in the range of about 10 ps to 100 ps. Thus, when a high-intensity pulse of energy is applied in a sub-threshold duration, the mechanism of layer removal can be characterized as a chemical alteration of surface molecules, or more specifically an electrochemical-tissue interaction since the energy is applied by means of an intense electrical field. In contrast, if the pulse duration of energy application is at an above-threshold level (e.g., in the ms range) with sufficient energy to cause damage, the mechanism and characteristics such of ablation would differ. That is, above-threshold energy delivery would cause damage that is largely thermal in nature and characterized by vaporization, melting, denaturation, fracture, etc. (In this above-threshold energy delivery modality, the electron kinetic energy transfer to the material's lattice structure is dependent on thermal diffusivity, a material property which expresses the ability of heat to diffuse and is equal to the square root of the ratio between heat conductivity and specific heat capacity). The present invention, however, is directed to ultrafast pulses (subthreshold duration) of energy application that create a critical density plasma from a thin surface layer. More specifically, the intensity of the electrical field (or discharge) and its absorption in the surface layer results in volatilization of macromolecules in the layer thus causing actual ionization of the thin layer thereby removing bulk. The energy burst is absorbed non-linearly and produces quasi-free electrons which, in turn, may act as seed electrons to cause an electron avalanche by various ionization processes. (Various ionization processes fall within the scope of the practice of the method, e.g., collisional ionization, multiphoton ionization, and field ionization). These ionization processes lead to irreversible alteration in the surface of the structure as ejecta (gas and bulk material) is ejected from the layer. It is believed that a very high fraction of the applied energy is removed by the high-velocity ejecta. Thus, any instantaneous high temperatures caused by the energy application are removed from the layer by the plasma formation process. It is further believed that mechanical shock waves to the bulk material will be insignificant compared to energy applications at above-threshold levels as defined above. At the subthreshold energy duration applications proposed herein in accordance with practice of the method, there will be insufficient time for lattice coupling, thus resulting in insignificant thermal diffusion-induced collateral damage to the structure.
• A further desirable consequence of using such ultrafast pulse of energy application for surface layer removal is that the method is relatively insensitive to hydration and density of the targeted surface layer, and is entirely chromophore independent. The drawback to the layer-by-layer plasma-mediated process disclosed herein is that the ablation rate, defined generally as the depth of layer removal per pulse, is small. That is, each pulsed energy application will only remove a layer having a thickness measured in μm's (microns). It is postulated that layer removal rate will range from about 1 μm to about 200 μm within the anticipated energy application parameters (from 0.1 J/cm.²to 1000 J/cm.²; or 0.1 J to 10 J per pulse). In order to overcome the low rates of material removal per pulse of energy in the typical case that needs substantial volumetric removal, the repetition rate of pulsed energy application must be high. This operational principle of the invention will be described below in Section I(C).
• B. Operational Principle: Photoionization of Neutral Gas and Confinement by Shape Structure and/or Fluid.
• The previous Section I(A) described a means for plasma-mediated cold electrochemical ablation of layers of body structure, but to construct a system feasible for surgical use, it is necessary define operational principles for spatial control of the energy application at the targeted layer to cause molecular volatilization. The operational principles according to this aspect of the invention relate to (i) providing means for creating an electrically conductive (partially ionized) gas volume proximate to the layer that is targeted, since the plasma-mediated ablation process described in Section I(A) can only occur in such a condition; and (ii) providing means for at least partially confining the ionized gas volume in its non-equilibrium state for a sufficient time interval to create the intense electrical field therein to cause volumetric removal.
• The present invention utilizes a probe with a distal working surface that in placed proximate to the targeted site for energy delivery. Thus, it is necessary to create the non-equilibrium ionized gas (an initial plasma) generally about this working surface. The invention utilizes a concept novel to biomedical applications for photoionizing a neutral gas volume introduced to the working surface. In such photoionization, a high-energy photon (e.g., from a UV source) irradiating the neutral gas may interact with an ionic electron leading to removal of that electron from the ion. To photoionize an ion requires a photon energy greater than the binding energy of the electron. As photons increase in energy (wavelength dependent), the cross-section for photoionization of a particular electronic state is zero until at a certain point the cross-section jumps to a finite value, which is termed a photoelectric edge. The method of the invention thus selects a radiation source characterized by photon/wavelength energies beyond the photoelectric edge as it relates to the selected neutral gas composition (for purposes of the disclosure, the gas may be any ionizable gas compatible with biomedical application, e.g., air, nitrogen, oxygen, CO₂, etc.). In the case of such photoionization, the departing electrons must exchange virtual photons with the nuclei for the process to occur. Such photoionization, therefore, tends to preferentially remove inner-shell (i.e., K-shell) electrons since these can most readily interact with the nucleus. Due to this effect, this process general leaves highly excited ions. After photoionization by photons of energy, the liberated electrons possess a kinetic energy and successive electron-electron collisions distribute this energy throughout the electron population with such kinetic energy being thermalised into a surrounding plasma. The non-equilibrium plasma thus created at the working surface of the probe and at the surface layer is capable of interfacing an intense electrical field (electrical discharge) with the targeted layer to cause the electrochemical ablation described in Section I(A). It is postulated that the photoionization of the neutral gas volume occurs within fs or ps and the duration of UV light pulse for such photoioization is described below in Section I(C) relating to repetition rates
• In accordance with practicing this method of creating a photoionized gas volume (non-equilibrium plasma), another aspect of the invention relates to confining or containing the ionized gas in its non-equilibrium state proximate to, or in contact with, the layer targeted for ablation. Essentially, two operational principles are employed to maintain the plasma's condition for sufficient duration to allow the high-intensity electrical discharge therethrough. First, the targeted surface layer is preferably immersed in a fluid environment (the fluid being any suitable water, non-conductive water-based solution or a saline solution, or a hydrogel) to prevent the ionized gas from rapid dispersion into the surrounding environment. In a surgery in the interior of a patient's body, such as an arthroscopic procedure, the standard use of saline immersion is compatible with the invention. By the term immersion, it is meant that the surface layer is covered in any suitable fluid to any particular depth, and the depth may be very slight and still accomplish the purpose of preventing dispersion of the ionized gas volume. For example, the fluid immersion may comprise a layer as thin as a film if it provides a seal between a perimeter of the working face and targeted layer to briefly contain the plasma. Thus, the method of the invention may be used on surface layers of body structure exposed to the atmosphere, such as a patient's skin, when covering the structure with a thin gel or water.
• A second (optional) principle that is utilized to confine the plasma is the provision of a shape structure at the working surface of the probe, such as a concavity to at least partially confine the photoionized gas. This shape structure also is useful for controlling the volume of ionized gas which will play a role in the plasma-mediated transfer of energy to the targeted surface layer. This shape structure, as well as particular dimensions of an exemplary embodiment, will be described in Section II below.
• C. Operational Principle: Controlled High Repetition Rate of Pulsed Energy Applications.
• The above Sections described a novel pulsed plasma-mediated ablation process that occurs, per pulse, in a time interval that may range from picoseconds to microseconds. In the sequential energy deliveries and plasma formations, only a thin layer of tissue is removed by the electrochemical-tissue interaction. In order to provide functional volumetric removal, the ultrafast pulsed energy event must be repeated at a high rate, and this Section describes operational principles relating to the selection of such a repetition rate. At a theoretical high repetition rate, there will be a high rate of volumetric removal. However, if the repetition rate is too high there may be collateral damage from thermal effects conducted to the surface layer by the plasma, which would defeat the objective of the invention in providing a substantially cold volumetric removal process. While it is postulated that the electrochemical-tissue interaction will occur without substantial thermal effects, a succession of ultrafast plasma creation and decay events may build up thermal effects in the plasma that would be conducted to the surface layer thus being capable of causing collateral thermal damage.
• The operational principle in determining a maximum theoretical repetition rate for pulsed energy applications concerns the relationship between duration of energy absorption effects by the surface layer and the layer's confinement of heat, which thus may result in unwanted collateral thermal damage. The operative construct is the so-called thermal relaxation time, and is defined as the time required for significant cooling of a defined volume of a body structure that has been elevated in temperature. Thermal relaxation is often defined as the time required for an elevated tissue temperature to be reduced by 50 percent. Many processes are involved in such cooling, such as conduction, convection and radiation. Macroscale conduction cooling in body structures probably dominates, but microscale radiational cooling at a very small target site proximate to a plasma may be important. For targeted sites on structure in a patient's body in laser applications, the rule of thumb is that the thermal relaxation time in seconds approximately equals the squared dimension of the targeted site in mm. (For example, a 0.5 μm size structure (5×10.⁻⁴mm.) will substantially cool in about 250 ns (25×10.⁻⁸seconds)). In the case of the inventive method disclosed herein, the fluid immersion aspect of the method is advantageous and will help provide rapid thermal relaxation. The fluid further may be pre-cooled which is beyond the scope of this disclosure.
• In accordance with practicing the principles of the method, it is postulated that ultrafast pulses of energy will be absorbed in the range of 100's of ps to 100's of ns. It is further postulated that repetition rates in the range of from about 10 Hz to about 500 Hz (or even 1000 Hz) are possible without exceeding the relaxation time of the surface layer. At this time, the repetition rates are theoretical and are to be explored with bench tests. As a practical matter, the timing of controlled flows of a neutral gas to the working surface and irradiation of the gas volume may prevent extremely high repetition rates. It is believed that with repetition rates in range of 2 Hz to 100 Hz, layer removal rates could be as high a 1 mm./s while maintaining the desired minimal collateral damage characteristics of the plasma-mediated ablation.
• D. Operational Principle: Plasma Luminescence Feedback System for Tissue Layer Differentiation.
• A final operational principle underlying the practice of plasma-mediated ablation relates to the potential need for diagnostic means in the selective layer removal process to prevent the removal of layers of structures that must be protected. In many procedures relating to tissue removal by a surgeon, the ablation process will be initiated and terminated on the basis of the surgeon's visual observation of the targeted surface layer and evaluation of the ablation process. However, when ablating surface layers in the interior of a patient's body, particularly in a fluid environment, endoscopic observation of the ablation process may be poor. A principal reason for the author's investigation of plasma-mediated ablation in a fluid environment is that the inventive method advantageously will allow spectroscopic analysis of luminescence of the plasma, and control signals may be derived therefrom to terminate the ablation process. In other words, as each successive plasma is formed by the pulsed high-intensity electrical discharge, an opportunity is provided to use tissue layer differentiation diagnostic procedures based on spectroscopic plasma emission signatures. Such a spectroscopy system would utilize an optic fiber for collecting emitted light from the plasma generated by the volatilization of the surface layer and ejecta in the plasma. The light would be dispersed and analyzed by an analyzer system, such as an intensified, gated, optical multi-channel analyzer/spectrograph. Emission peaks characteristic of different tissue types would be used as reference data within the analyzer system. Thus, when the system detected emission characteristics of material that is not targeted, a signal would be provided to the controller to terminate the ablation process. It is believed this type of feedback system is novel to any electrosurgical ablation modality, and is made possible only because the practice of the method includes the creation of successive microplasmas at the targeted site. Further, this type feedback signal system is novel in that it can be utilized in a fluid operating environment. (Optical feedback systems based on spectroscopy have been tested with forms of laser energy delivery, but such laser systems cannot operate in a fluid environment. See, e.g., B. M. Kim, M. D. Feit, A. M. Rubenchik, B. M. Mammini & L. B. Da Silva,Optical feedback signal for ultra short pulse ablation of tissue, Appl. Surface Sci.127-129(1998) pp. 857-862.)
• II. Construction of Exemplary Type “A” System for Plasma-Assisted Cold Ablation
• Referring toFIG. 5, an exemplary Type “A” embodiment ofPASCAL system5 is shown which includesprobe10 and a remote energy sources in block diagrams. In this disclosure, the workingsurface15 ofprobe10 is adapted for positioning proximate to a targeted site on a surface layer of body structure to accomplish cold plasma-mediated ablation of the layer. The term ablation is used to characterize the surface layer removal process, and other descriptive words may be used interchangeably herein, such as, breakdown, decomposition, disintegration, obliteration, removal and volumetric removal to describe and define the plasma-mediated process that causes layers of a structure in, or on, a body to be altered, broken down, destroyed, damaged, or fragmented and ejected from the surface layer. The term structure of a patient's body as used herein is intended to be inclusive of any composition in a patient's body, and principally encompasses biological tissues but also is intended to describe all other body structures (some of which are sometimes not termed tissue) such as calculi, accretions, deposits, occlusions, bones and teeth, and the like.
• Theexemplary probe10 of the system comprises anelongate extension member20 having proximal (handle) end21 and a distal working surface end indicated at15 with a cross-section or diameter ofbody22 being about from 1.0 mm. to 5.0 mm. (not limiting), the extension member defininglongitudinal axis27. The extension member may be fabricated in a variety of configurations to mechanically support at least one active electrode about in the workingsurface15 and to allow the operator to position the workingsurface15 in relation to a targeted site on a surface layer by manual or robotic manipulation of theproximal end21 of the extension member. Typically, theextension member20 comprises a small cross-section member or tube being dimensioned for introduction into the interior of a patient's body through a trocar (cannula) in a minimally invasive procedure, for example in arthroscopy, laparoscopy, or another thoracoscopic or endoscopic procedure. The elongate member may have any suitable length. The elongate member also may be rigid or flexible. A flexible probe may be provided with pull wires, shape memory actuators, and other mechanisms known in the art for articulating a distal end for positioning the working face proximate to the targeted site.
• InFIG. 6, it can be seen that workingsurface15 defines ashape structure28 comprising a concave or recessedportion30. The recessedshape structure28 is adapted to at least partially contain a neutral gas and its photoionized counterpart and the concavity may be of any suitable dimension or extend inwardly (proximally) to aninterior chamber portion32 and fall within the scope of the invention.FIGS. 7A-7B show sectional silhouettes ofalternative shape structures28 withFIG. 7A depicting a more concave shape structure suitable for use in an immersion fluid F in a workspace WS over tissue layer L andFIG. 7B showing a slight concavity (a lack of concavity altogether may fall within the scope of the invention) for use with a more viscous fluid VF or gel layer over tissue layer L.
• Returning toFIG. 6, probe10 carries a optical delivery or light-channeling means such as an optical fiber35 (or fiber optic bundle, wave guide or other light-channeling means) incentral portion37 ofextension member10 which is adapted to direct light energy from a high-intensity source orUV source40 as described above in Section I(B). The optical delivery subsystem depends on the design parameters of the tissue removal system and may alternatively comprise a fiber optic cable, an articulated arm with mirrors, or an open beam delivery system including coated reflectors and lenses to focus the radiative beam. In this embodiment, the optic fiber withcladding42 is carried incentral lumen44 of theextension member20. In any event, the workingsurface15 is carried at a distal end ofprobe10 to allow the operator to maneuver the working surface into proximity to a targeted surface layer. It should be appreciated that the distal termination of thefiber35 may have itscladding42 partly removed (not shown) to cause photoionization along a distal portion of passageway orlumen44.
• Acomputer controller45 is operatively connected to the high-intensity light source40, and controls the activation of the source, as well as its pulse repetition rate, in response to control signals that are provided by the system operator. Any sort of on-off switch (foot pedal or hand switch not shown) is connected tocontroller45 and provides activation signals in response to the actuation of the switch. The pulse repetition rate may be set by the operator by a form of rheostat control connected tocontroller45 which increases or decreases the repetition rate in response to the operator selection. It should be appreciated that any suitable high-intensity UV source40 may be suitable for delivering energy along the light-channelingmeans35, and a conventional discharge lamp known in the art is preferred together with optional filters, combiners, and associated optics may be suitable to perform the method of photoionization aspect of the method described above (i.e, a discharge lamp passes an electric current through a rare gas or metal vapor, wherein electrons collide with gas atoms exciting them to higher energy levels which then decay to lower levels by emitting light; mercury, hydrogen, deuterium, Ne, Ar, Kr, and Xe discharge lamps all may useful for the photoionization aspect of the method). The light source is preferably remote and carried to probe10 by a flexible fiber (not shown) but the light source also could be carried in a handle portion of the probe. Thelight source40 also may be an excimer laser, such as an OPTex system by Lambda Physik, Inc., 3201 West Commercial Blvd., Ft. Lauderdale, Fla.
• The UV energy radiated fromsource40 is pulsed as is known in the art by acomputer controller45 capable of controlling the delivery of light pulses having a pulse duration ranging from about 100 ps to tens of ms with a repetition rate ranging from about 1 Hz to 1000 Hz. In the exemplary embodiment ofFIG. 6,extension member20 may carry a single optical fiber or a fiber bundle having any suitable diameter, for example ranging from about 100 μm to 500 μm.
• FIG. 6 further shows a neutralgas delivery source50 that communicates with theinterior lumen44 or passageway inmember20 that is configured concentrically aroundfiber35. Thelumen44 extends to its distal terminus52 at the interface with the concavity orshape structure28 withweb portions54aand openingportions54bmaintaining the fiber in a central portion oflumen44. It should be appreciated that any fluid-tight passageway may be provided and it need not be a concentric relative to thelight channeling means35. The system further provides a positive (+) pressurization system indicated at55 for moving the neutral gas to the working surface25 and may include any pump means or gas metering means known in the art, such as a peristaltic pump. As illustrated inFIG. 5, the neutral gas pressurization system55 is operatively connected to thecontroller45 for timing gas inflows, or pulsed inflows, relative to the irradiation of the gas volume with photonic energy from thephotoionizing source40.
• Referring toFIGS. 5-6, anelectrical source60 is provided as the energy delivery means to perform the electrochemical ablation, and the intense electrical field in the photoionized gas volume is created via an electrode arrangement indicated at65. The exemplary activeconductive electrode65 ofFIG. 6 is carried in theconcave shape structure28 of the workingface15. In accordance with the practice of the invention, theelectrode arrangement65 will have one active surface portion66 with a particular surface geometry shape that is adapted to enhance the intensity of the electric field and the current density at the time of each pulsed energy delivery. For this reason, such surface geometry preferably includes at least one projecting portion or sharp edge portion at the active surface. In the exemplary embodiment ofFIG. 6, the surface geometry is characterized by a plurality of two projectingsharp edges66A-66B that extend into theconcave shape structure28 of workingface15. It should be appreciated such preferred surface geometry may include only one conductive electrode portion, or a plurality of micro-scale sharp edges that may be characterized simply as surface roughness on the active surface of the electrode, and as such may be provided by any suitable chemical, electrochemical or abrasive method to create micro-edges on the active surface portion to thus enhance the high electric field intensities between the active electrode surface66 and the targeted surface layer. In any type of electrode arrangement, the electrodes edges or projecting portion may be isolated but are the same source polarity as they will be electrically coupled to with a commonelectrical lead67 either in theproximal end21 of the extension member or at theelectrical source60. The exemplaryactive electrode65 is shown as extending aroundaxis27 of theconcave portion28 but it should be appreciated that the electrode could be located at any other suitable location about the working surface. Referring still toFIG. 6, theelectrode65 is coupled to a conductive lead orwire element67 that extends throughbody portion22 ofelongate member20. Thebody portion22 ofextension member10 may be any suitable insulated material such as a ceramic, plastic, glass or a combination of separate elements as are known in the art.
• In the block diagram portion ofFIG. 5, it can be seen that thesystem5 has anelectrical source60 that is connected toelectrode arrangement65. Theelectrical source60 may be any suitable electrical energy source as is known in the art than is capable of delivering high intensity electrical current, for example in the range of 10 to 2000 volts. Theelectrical source60 of the present invention preferably delivers a high frequency voltage that may be selected from a range to generate average power levels ranging from a few milliwatts to hundreds of watts depending on the targeted surface layer and the desired the rate of removal. Thecontroller45 associated with theelectrical source60 would allow the operator to select the voltage level according to the specific requirements of surface layer removal procedure. It is postulated that the voltage applied between the active electrode and the surface layer and return electrode will be in the range from about 50 volts to 2000 volts. Theelectrical source60 is coupled tocomputer controller45 to control the timing of energy delivery in relation to the timing of the photoionization step, and also may be programmed with suitable software72 to allow independent modulation of parameters of electrical energy delivery, including: (i) voltage, current and peak electrical power per time interval; (ii) the length of a time interval of current delivery; and (iii) the profile of energy delivery within each time interval, to allow 1 to 1000 Hz repetition rates.
• Thecomputer controller45 of the invention depicted inFIG. 5 may further be provided with feed-back circuitry known in the art for measuring the impedance between the active electrode surface66 and the targeted surface layer. The impedance level will change, as will be described in the steps of the method shown below in Section III, as the neutral gas volume is photoionized, and thus feedback of the change in impedance can be used as a control signal for initiating the step of high-energy electrical energy delivery.
• III. Method of Use of Type “A” System for Plasma-Assisted Cold Ablation of Surface Layers.
• In practicing the method of the invention in a laminectomy/disketomy procedure to treat a herniated disc by removing surface layers of tissue, the patient is be prepared in any conventional manner with anesthetics andFIG. 8A depicts theelongate extension member20 and its workingface15 being advanced into a working space WS to the targeted layer L. The surgeon may advance the workingface15 under endoscopic vision or by other manners known in the art (not shown), such as being assisted by real-time imaging.FIG. 8B represents an enlarged view of the workingface15 in a workspace that is filled with a fluid80. FIGS.8B &9A-9E show that the patient's body is coupled to a ground pad or return (−)electrode85 as is known in the art.
• Now referring toFIG. 9A, a sectional view of the distal end ofextension member20 is shown positioned proximate (within about 1 mm. or less), or pressed gently against the targeted layer L (it should be appreciated that layer L may be the surface layer of any body structure).FIG. 9B then shows actuation of the system bycontroller45 wherein a neutral gas NG is introduced throughlumen44 into the workingface15 with the volume being captured by theconcave shape structure28 and the surroundingfluid80 which prevents the gas from rapidly dispersing.
• Now turning toFIG. 9C, thecontroller45 after a pre-selected time interval irradiates the neutral gas volume with UV energy viabeam82 that is carried throughoptic fiber35 fromsource40.FIG. 9C thus depicts the step of photoionizing the neutral gas volume to create a conductive plasma indicated at P₁that will remain in such non-equilibrium state for a first brief time interval. InFIG. 9D, thecontroller45, after a pre-selected very brief time interval, triggers thepower source60 to deliver an intense electrical energy pulse from the active electrode surface66 across the plasma to layer L (that is coupled to return electrode).FIG. 9D thus depicts the volatilization or commencement of ionization of layer L which, in effect, begins to alter the condition with other species to form an altered plasma indicated at P₂. InFIG. 9D, the volatilization of the surface layer L removes material from the layer by application of an energy quantity to the layer with ejecta E depicted in the plasma P₂, wherein the ejecta is essentially gases and possibly material fragments (depth of material removal exaggerated inFIG. 9D for a single plasma creation event). In a very brief time interval subsequent to the ultrafast fast event depicted inFIG. 9D, the plasma P₂will decay. Thereafter a repetition of the plasma-mediated material removal process occurs as thecontroller45 repeats the plasma-mediated ablative pulses in accordance with the events depicted inFIGS. 9A-9D.FIG. 9E shows the next step in this sequence with the neutral gas NG being introduced into the workingface15. It should be appreciated that the probe may be translated across layer L to remove material in a path or maintained in a stationary to drill a hole in the layer, either of which may be an element of the procedure. The distalmost surface of the probe preferably is to be held gently against the tissue layer, of slightly above the tissue layer In a diskectomy procedure as indicated inFIG. 9A, material is removed as required under endoscopic visualization, without thermal collateral damage to surrounding tissue.
• The method of the invention may further include the step of analyzing the emission spectra by means of thefiber optic35 which is coupled to a remote plasma luminescence spectroscopy system andcontroller45. For example, the plume following a ultrafast plasma creation event in removing disc material in the exemplary procedure will provide emissions that can be compared with reference data for a known material in a disc, such as calcium If the emissions from the plasma exhibit characteristics that compare with non-targeted disc material, such as a nerve, the spectroscopy system can signal thecontroller45 to terminate energy delivery.
• IV. Construction of Type “B” System for Plasma-Assisted Cold Ablation.
• A Type “B” embodiment (not shown) is very similar to the Type “A” embodiment except that the central core of the probe carries an optic fiber that is utilized to collect emitted light emissions from the plasma P₂indicated inFIGS. 9D-9E. The emission peaks of the plasma P₂are fed to a spectroscopic analyzer system90 (seeFIG. 5) and compared to the peaks in reference data to determine whether non-targeted tissue types have been affected by the ablation. The system is connected tocontroller45 and may be programmed to terminate the ablation process within ns or ms.
• The Type “B” system also includes impedance-measuring circuitry for triggering the delivery of electrical energy to the (photoionized gas) plasma P₁as indicated inFIG. 9C. In other words, instead of providing programming incontroller45 that triggers energy delivery in a pre-selected time sequence, the impedance-measuring circuitry can continuously measure impedance within the region between the active electrode surface66 and layer L which is altered by (i) the photoionization of the neutral gas volume as shown inFIG. 9C as well as its confinement, and (ii) the distance between the workingface15 and layer L.
• Another aspect of the Type “B” embodiment of the invention (not shown) is the provision for aspiration of ejecta and fluid from the workspace. For example, if the targeted layer is a portion of malignant tissue, it may be useful to sequence aspiration of the ablated tissue fragments (along with gas and fluid) from the workspace. The controller would be adapted to provide such pulsed aspiration between pulsed applications of energy. The passageway for receiving such removed material particles would preferably be a concentric lumen around theextension member20 ofFIG. 6, but it could also be any type of interior passageway and fall within the scope of the invention.
• V. Construction and Method of Use of Exemplary Type “C” System for Plasma-Assisted Material Removal.
• In a previous part of this disclosure (see “Summary and Objects of the Invention”), a number of processes were described to cause, induce or develop ionization of a captured neutral gas volume (or bubble), and thereafter terminate ionization of the gas, in an interface between a probe working end and a targeted site ts. Such an instantaneously and independently ionized gas volume can then cause an intense application or arc of electrical energy from an electrode to the targeted site ts across the gas volume to volumetrically remove surface layers of an anatomic structure. Several ionization processes were described above, viz., photoionization (PI), field ionization (FI), thermal ionization (TI) and the ionization of surface analytes from a solid material. In this Type “C”embodiment205, the use of independent field ionization (FI) means is described as an option in Section V(C) below and at times referred to as the first energy source. In addition, a working end carrying a microchannel plate (MCP) is disclosed in Section V(B) below which comprises an electron-emissive coating on a microchannel structure that, it is postulated, can enhance the energy of a plasma for causing volumetric material removal. Both the Type “A” and “C” systems utilize thesame gas source50 for introducing the neutral gas volume to working surface. The Type “C” system also is coupled tocontroller45 and electrical source60 (second energy source) as described above that allows for the time-controlled and volume-metered introduction of the neutral gas volume (media m₂) to the working end. All parameters of electrical energy delivery may be programmed to generate trains of energy applications to the targeted site ts at selected repetition rates, or in a continuous mode, as described in the Type “A” system above.
• A. Intense Pulsed Electric Discharge Mode of Operation of Type “C” Working End
• More in particular, the Type “C” system ofFIGS. 10 and 11 depicts an exemplary workingend210 of aprobe member212 that is adapted for use in a skin resurfacing procedure. For example,FIG. 10 shows the working end being translated over a skin surface very close to a patient's eye, which may be problematic for laser resurfacing. As will be described below, energy applied by the working surface to the skin can be modulated easily to cause very thin layer ablations for sensitive areas, such as periocular regions, in manners not possible with a laser. Also, the same instrument may deliver a first selected intensity of energy to the main portions of the patient's face, and a second selected energy intensity to periocular regions.FIGS. 10-11 show the exemplary working end with a narrow width-of-face dimension indicated at wf in comparison to a length-of-face dimension If across the workingsurface215. In an instrument adapted for unidirectional translation or painting across tissue, such as in skin resurfacing, it is preferable to have such a narrow width with substantially parallel sides (transverse to the direction of translation) to control the number of successive energy-tissue interactions that occur as the workingface215 passes over any location. As will be described below, any width dimension across a working face may be defined by the number of features (or microchannels) at which a discrete energy-tissue interactions are localized.
• In this Type “C”system205, an exemplary workingend210 of a probe member212 (seeFIGS. 11 & 12) has a workingsurface215 that carries a microchannel structure comprising of a plurality of channels (e.g.,220a-220dinFIG. 12) having open distal terminations222a-222din the working surface. The microchannel structure can be fabricated by the same processes as a micro-channel plate (MCP) or may be fabricated by a plasma-processing means known in the MEMS field (microelectrical machining). Theinsulator material224 of the working surface may be glass, plastic, ceramic, a form of silicon or any other suitable material. As an example of fabricating the microchannels, a microchannel plate (NCP) is a device that is commercially available for photo-detection purposes and may be used in the present invention, both for the basic microchannel structure, and optionally for electron avalanche means as will be described below. In an MCP, a tubular cladding glass is mechanically supported in its bore by the insertion of a rod of etchable core glass to produce a potential microchannel. The assembly is then pulled through an oven and drawn down in diameter to produce a microchannel (after the core is etched away). A plurality of such drawn-down assemblies then are stacked and drawn down through the oven until a selected diameter is achieved for the core. Thereafter, the assembly is fused together and the cores are etched away leaving the microchannel structure. While commercially available MCP's typically may have channels or capillaries ranging from about 5_m and 25_m in diameter, for photodetection purposes, it can be seen that any suitable diameter of channels can be fabricated by the above methods. Another manner of fabricating the microchannel structure of the present invention is to use conventional semi-conductor processing methods to create both the microchannels in an insulator material and the electrode layer arrangements as will be described below.
• InFIG. 12, an enlarged sectional view of a very small portion of the microchannel structure shows several microchannels with open distal terminations222a-222din the workingsurface215. In any embodiment, an electrode arrangement or layer indicated at225 (also called the ablation electrode) is provided with exposed surfaces227a-227dthat interface with volumes of media m₂(a gas described in detail below) contained within the microchannels to thereafter apply energy to tissue. In this exemplary embodiment, a microchannel at its open end has a cross-section that is less than about 500 μm. More preferably, the microchannels or chambers portions have a selected cross-sectional dimension at the open terminations222a-222din that ranges from about 5 μm to 400 μm (seeFIG. 13). Still more preferably, the microchannel open terminations222a-222drange from about 25 μm to 200 μm. The open terminations are spaced apart by aninsulator portion224 ranging in dimension from about 5 μm to 500 μm. In any Type “C” embodiment, the electrode exposed surfaces227a-227dare spaced inwardly or proximal from the distalmost working surface215 a selected dimension d₂that ranges from about 5 μm to 500 μm, in general varying in dimension in direct proportion with the cross-section of the channel and the voltage levels used. In other words, the electrode exposed surfaces227a-227dhave a covering layer ofinsulator material224 that prevents direct contact of any electrode with tissue in contact with thesurface215.
• InFIG. 12, an objective of the invention is illustrated wherein a particular volume of media m₂is shown captured in the distal portion of twochannels220cand220d.The method of the invention creates the discrete transient media volumes indicated at v, and thereafter ionizes and deionizes such volumes v, within microsecond intervals to controllably cause electrical energy to cross the media volume v from an electrode exposed surface (e.g.,227a-227d) to the targeted site ts. InFIG. 12, the media volumes v are shaded to indicate an ionized condition as would occur when UV light is radiated through a light-channel35 withinmember212 exactly as described in the Type “A” embodiment (seeFIG. 5C). For purposes of explaining the method of the invention,FIG. 14A shows the media volume v independent of the working end structure wherein the exterior boundary of the media volume v in herein termed a surface engagement plane sep wherein the media surface engages both the exposed electrode surface (e.g.,227a-227d) and targeted tissue ts to deliver energy to tissue.FIG. 14B shows a single media volume v in a perspective view of an end portion of amicrochannel220c.InFIGS. 14A-14B and subsequent Figures, the media volume v is illustrated with a proximal surface portion (with hatched graphics) that is in contact with the electrode surfaces (e.g.,227a-227dofFIG. 12) herein called an electrode engagement area indicated at ee. In this disclosure and other applications cross-referenced herein, the concept of controllably forming a volume v or bubble of media m₂between an electrode surface and a precisely localized target site ts is a key component of the method of the invention.FIG. 12 shows the targeted site ts as a grid of arbitrary units, for example at the smallest scale from about 5 μm to 10 μm, in which the volume v engages or contacts the targeted site ts at a precise location to thereafter cause an energy-tissue interaction eti proximate to the microchannel open termination222a-222dthat will approximate the cross-sectional dimension of that microchannel termination.
• As can be seen inFIGS. 11-12, two other pairedelectrode layers235 and245 are provided having electrode exposed surfaces237a-237dand247a-247dwithin the microchannels, respectively. This electrode pair, and more particularlyelectrode245, is spaced apart fromelectrode layer225 by a suitablethickness insulator layer224 to prevent the possibility of unwanted electrical interactions betweenelectrode layers225 and245. Theelectrode pair235 and245 cooperate with each other to perform an optional method of the invention that utilizes high voltages described below, and thus thedistal electrode245 is spaced a selected dimension d₃from the distal workingsurface215 to prevent an electrical discharge to the targeted site ts from electrode245 (seeFIG. 13). The electrode layers235 and245 are spaced apart a selected dimension indicated at d₄for causing an intense electrical field between the electrodes that cooperate with an electron-emissive surface coating252 in the microchannel interior further described below. Allelectrodes225,235 and245 are coupled to theelectrical source60 by separate leads. The use ofelectrodes235 and245 offer an optional enhanced mode for applying energy delivery to the targeted site ts (described below). In a basic energy delivery modality, the photoionization means andsingle electrode layer225 can be utilized to cause precise volumetric tissue removal, which is similar to method performed by the Type “A” system inFIGS. 5A-5E above and is briefly described next.
• In a first operational mode of the workingend210,FIGS. 15A-15E graphically depict the use of the instrument and itsdistal working surface215 to volumetrically remove surface tissues by causing a plurality of discrete and spaced apart, micro-scale, precisely localized energy-tissue interactions eti or ablations.FIG. 15A-15B show a perspective view of view three adjacent media volumes v within the workingsurface215, microchannels220a-220cand open terminations microchannels222a-222cin phantom view. The open terminations222a-222care within a dimensional range r of the surface of the targeted site ts which again is graphically illustrated in a grid measured in arbitrary units. Of interest, the range r is defined as a particular dimension that is achievable by the method of the invention for creating a directed path or conductive path cp of electrical energy irradiation beyond the workingsurface215 to deliver energy to tissue. In other words, it is postulated that UV radiation through the microchannels220a-220cwill illuminate a conductive path cp extending substantially beyond the workingsurface215 and within media ml (the surrounding non-conductive gas environment) to the targeted site ts. The substantial confinement of this conductive path within surrounding media ml will exist for a very brief interval before its ionization degrades and blends with the surrounding gas media m₁. However, during the interval in which the conductive path is substantially intact, the path cp will direct electrical energy through the free space fs beyond the working surface to the targeted site ts. In this respect, the conductive path cp in combination with the timed delivery of electrical energy from electrode engagement region ee exhibits the key characteristics of laser beams insofar as utilized for laser-tissue interactions. That is, controlled amounts of energy can be delivered through free space to a precisely localized point on the targeted site ts. The method of the invention has a limited free space range r of energy propagation, when compared to a laser, but it is believed the invention will provide a range r that is from about 100 μm to 2000 μm for working surfaces with the larger above-specified microchannel terminations222a-222c.
• Again referring toFIGS. 15A-15B, the first Figure depicts (i) a neutral gas media such as the environment (air or m₁) stabilized in and about the working surface or preferably (ii) a selected biocompatible neutral media m₂(e.g., CO₂, argon, etc.) flowing through the microchannels from a source as detailed in the Type “A” embodiment. At this point in time, or a slight time interval prior to the ionization step ofFIG. 15B, electrical potential is created at the electrodes and engagement area ee (e.g., at a time T₀). Optionally, the electrical potential is initiated contemporaneously with the ionization step ofFIG. 15B.FIG. 15B depicts the next step of the invention wherein the media volumes v that extend from the electrode engagement area ee to the targeted site ts are ionized (e.g., at a time T₁), which is indicated graphically by shading and further indicated as media m₂being altered to media m₂′. In this mode of operation, the media is ionized by photoionization means (first energy source) comprising UV radiation delivered to the proximal end of the microchannel structure, based on the same means described in the Type “A” embodiment which need not be repeated. As can be seen inFIG. 15B, each open microchannel termination222a-222cis within range r of the targeted site and the ionized media m₂′ extends across any freespace fs to interface with the targeted site in an area substantially equivalent to the cross section of the open termination222a-222c.
• FIG. 15C shows a view very similar toFIG. 15B and depicts the range r of the conductive path cp within the surrounding non-conductive media ml that will occur for a brief interval, as described above.FIG. 15D graphically represents a result of the ionization step ofFIGS. 15B and 15C wherein the now conductive media m₂′ of the volumes v instantly delivers electrical energy across the volumes v from the electrode engagement areas ee to regions of the targeted surface ts engaged by the volumes v. The energy application is graphically depicted by waveforms w of the electric field or discharge inFIG. 15D.
• Of particular interest,FIG. 15E next graphically depicts the energy-tissue interactions eti that would occur practically contemporaneous with the energy application step ofFIG. 15D. It can be seen that a series of discrete, precisely localized, time-controlled energy-tissue interactions eti or ablations will be caused by the method of the invention and result in ejecta e of water vapor and cell debris. The intense energy potential at the electrode interface ee with the gas volume v is carried to the tissue surface to cause intense energy densities that ablate tissue by vaporization of thin surface layers for the brief interval that the ionized media m₂′ remains.
• The next step of the method of the invention (not shown) is (i) the termination of photoionizing UV radiation to the gas media in the microchannel structure thereby returning such gases to a non-conductive nature (seeFIG. 15A); and optionally (ii) the continuous or pulsed inflows of the neutral gas through the microchannel structure to insure the gas volumes therein are instantly returned to neutral. Contemporaneous with this step, the electrical potential at the electrodes is terminated.
• Following the above sequence of steps which occur in a micro-second time frame, the steps of the method are repeated after a very brief selected interval that exceeds the thermal relaxation of the targeted site, as described above. The time intervals for utilizing the photoionization means for switching the gas media from non-conductive to conductive may be repeated at a pulse rate between about 200 ns and 500 ms. Stated another way, the interval between repetitions of the complete steps of photoionization and electrical energy applications, may range from about 500 ns to 500 ms to insure thermal relaxation of the targeted site.
• It can be seen inFIG. 15E that energy application to a targeted site ts will result in a very even distribution of energy across the site having the dimensions of the width wf and length If of the working surface215 (seeFIG. 11). Further, it can be understood that by painting the workingsurface215 across the targeted site ts, an even ablation will occur in a path due to the large number of discrete energy-tissue interaction sites eti (seeFIG. 15E). In an early section of this disclosure, it was explained that in prior art ablation modalities, the distribution of energy densities and ablation effects across an energy application site were random, and the dimensions across any such energy application site also would be random due to the random size of the insulative bubble that is formed (see application of energy to tissue inFIG. 3) The workingsurface215 and method of the present invention thus solve the problem of uneven and random energy distributions across a targeted site by the novel micronization means of the invention, with respect both to the feature dimensions of the workingsurface215 and the resultant dimensions across a particular the energy-tissue interaction eti. By this means, an aggregation or grid of such discrete localized energy-tissue interactions eti (ablations) can be designed to comprise any desired dimension of an ablation area, for example to match the size of a prior art ablation if desired. Further, the present invention thus can be favorably compared to a laser energy-tissue interaction. In laser irradiation of a tissue surface, energy distribution across a site may be controlled largely by optics, with a desirable “top hat” energy distribution shown inFIG. 16A where energy is delivered evenly across an irradiated site, and the generally less preferred Gaussian energy distribution ofFIG. 16B where higher energy densities are caused in the center of the site with a bell curve defining a taper-off of the energy delivered toward the perimeter of the site. Thus, the present invention, by distributing a large number of discrete energy-tissue interactions evenly over a particular application of energy per selected time interval at a targeted site ts, it can be said for the first time that energy can be applied to a targeted body structure from an electrical source that effectively results in a substantially even “top hat” energy distribution across the site. It is believed that working electrode surfaces with features micronized as described above to perform the novel method of electrosurgical ablation can be used advantageously in every form of electrosurgical instrument used for ablation, for example, simple mono-polar cutting electrodes, ablation catheter working ends, stereotactic needle working ends used for precise tumor ablation in the brain or breast or elsewhere, and all other ablation electrodes. The micronization of the energy tissue interactions eti also limit collateral thermal damage to the level of insignificance due to the limited depth of any application of energy that is substantially confined within very thin surface cell layers.
• The workingend215 of the device ofFIGS. 10-11 may further be provided with a perimeter suction channel as is known in the art (not shown) for aspirating tissue debris from the targeted site at the working end is translated over the tissue. The open apertures or apertures of such a suction channel preferably would be spaced around the perimeter or edge of the microchannel structure.
• B. Alternative Energetic Plasma Mode of Operation of Type “C” Working End
• The previous section described the application of high intensity electrical energy in pulses to a targeted site ts to cause volumetric material removal wherein the ablation will cause substantially little collateral thermal damage to tissue due to (i) the micron dimension of the discrete energy-tissue interactions that ablate only very thin cell layers, and (ii) the thermal relaxation of the targeted site ts between timed applications of energy at the 100's or 1000's of discrete, localized sites. It is believed that an alternative mode of operation will prove possible with the Type “C” working end in which electrical energy is delivered continuously to the microchannel structure, along with optional means of enhancing such energy delivery, to cause sustainable highly energetic microplasma volumes about the open microchannel terminations222a-222c(seeFIG. 12) capable of volatilizing surface molecules over a selected time interval to cause volumetric material removal.
• More in particular, referring toFIG. 17, the electron avalanche means of the microchannel plate (MCP) structure may be energized in this alternative mode of operation to create the energetic microplasma indicated at m₂″ (i.e., m₂′identified ionized media in the previous mode of operation; m₂″ identifies the enhanced plasma of the alternative mode) about the exemplaryopen microchannel termination222a.The steps of this alternative method comprise initially delivering appropriate electrical energy to the pairedelectrode layers235 and245 of the microchannel structure, which is in the range of 100 to 2000 volts. Thereafter, the steps previously described are initiated; that is electrical potential is created atelectrode225 and then the UV source is triggered to photoionize the media volume v that is within the microchannel structure. In this case, as depicted inFIG. 17, the UV photons strike the electron-emissive surface coating252 of the microchannels between the pairedelectrode layers235 and245 and cause an electron spray (avalanche) indicated at es wherein the electrons can freely travel the minimal distance d₅to greatly increase in the free electron population of the microplasma m₂″ to assist in the molecular volatilization of the surface of the targeted site (seeFIG. 17). In this mode of operation, the electrical potential atelectrode layer225 may be continuous rather than pulsed to maintain the microplasmas at a high intensity, and if the dimension between the open microchannel terminations222a-222bis small, it is believed that an energetic plasma volume will extend in a layer substantially across and about the workingsurface215 to interface with the targeted site ts. This instrument and method, it is believed, will be able to create and sustain a sufficiently energetic microplasma to cause a true plasma-mediated ablation of tissue at voltages atelectrode225 in the range of 100 V to 600 V. At these sufficiently high energy levels (or voltage V), it is believed that energy in the range of 3.0 eV to 8.0 eV can be created to cause breakdown of the carbon-carbon bonds, carbon-nitrogen bonds, and other similar bonds in surface molecules. When comparing the system disclosed by Eggers et al (U.S. Pat. Nos. 5,873,855; 5,888,198; 5,891,095; 6,024,733; 6,032,674; 6,066,134) and commercialized as the Coblator™ system, it can be easily understood this prior art system expends much of its available energy to continuously thermally vaporize random elements (NaCl) within a cool liquid to produce random insulative gas bubbles over and about a large working end, which bubbles thereafter are ionized randomly by an intense electrical discharge therein and there across. In contrast, the present invention expends no energy to vaporize a liquid to produce the required gas volumes. The present invention independently produces and introduces a neutral gas into the working end. Further, the present invention utilizes both photoionization means and an optional electron avalanche means to energize the plasma volumes. Still further, the microplasma volumes are captured within the microchannel structure and such micron-sized volumes can efficiently sustain an energetic plasma.
• FIG. 18 illustrates a variation on the Type “C” working end ofFIG. 17 that provides a multiple layer MCP structure, in an optional chevron configuration, to further enhance the electron population of the microplasmas m₂″. The workingsurface215 again carries thesame electrode225. A first microchannel plate (MCP) layer (not-to-scale) indicated at260ahas pairedelectrode layers235aand245athat function as previously described. A second MCP layer (not-toscale) indicated at260bhas pairedelectrode layers235band245b.There may be further layers, and the purpose of the chevron pattern is cause the electron spray es from a more proximal layer to strike the walls of the more distal microchannel at an angle to thereby increase electron emissions.
• C. Alternative Field Ionization (FI) Mode of Operation of Type “C” Working End
• The previous sections have described the method of using a Type “C” working end wherein the ionization means comprise a light-carryingchannel35 and a UV source to deliver energy to the working end. Other ionization means independent of theablation electrode225 are possible have been disclosed (see, e.g., co-pending U.S. Ser. No. 09/317,768 filed May 24, 1999 (Docket No. S-QP-002) titledPhotoionized Gas Enabled Electrical Discharge Technique for Plasma-Mediated Cold Tissue Ablation) and are listed again in the first paragraph of Section V above. There may be requirements for certain instruments that make it difficult or expensive to rely on light-channelingmeans35 to deliver UV energy to a working surface. For example, it may be difficult to fabricate a light channel in an elongate catheter having a very small diameter. Also, it may be expensive to fabricate a light channel in an elongate introducer member in which the axis of the microchannel structure is transverse to the axis of the introducer.
• For this reason, a workingsurface215 with microchannel structure substantially the same as depicted inFIG. 12 may be used without photoionization means. Instead, the pairedelectrode layers235 and245 with exposed surfaces237 and247 within microchannels220a-220d(absent electron-emissive coating252) may be used to cause field ionization of an introduced neutral gas, with the other steps of pulsed energy delivery to cause tissue ablation the same as described previously (seeFIG. 19D).
• Referring toFIGS. 19A-19C, an exemplary elongate catheter-type device280 is shown that is dimensioned for introduction through a working channel282 of a gastroscope283 for the thin layer ablation of irregular or pre-cancerous cell layers in the mucosal lining mu of an esophagus, such as in a treatment of Barrett's esophagus (seeFIG. 19A). It should be appreciated that the working end could be used for skin resurfacing or any other thin layer ablation. For example, the catheter-type device280 may be from about 2.0 mm. to 4.0 mm. in diameter. The workingend285 of the device is aninsulator body286 and carries a microchannel structure having adistal working surface215 andelectrode layer225 substantially as described above (seeFIGS. 19B-19D). Referring toFIG. 19D, it can further be seen that the microchannel structure carries paired, spaced apart electrodelayers235 and245, the same as in the previous configuration ofFIG. 12 without electron-emissive coating252. Theelectrodes235 and245 are coupled to theelectrical source60 byleads287aand287b,respectively (FIG. 19B). Theelectrode layer225 is coupled to the electrical source bylead288. A simplified method of fabricating a microchannel structure for experimentation as shown inFIG. 19C (orFIG. 12) is to sandwich two MCP plates together as shown in more detail inFIG. 19D. The electrode layers235 and245 of the more proximal plate are coupled to the electrical source. Only theinner electrode225 of the distal MCP is coupled to the electrical source thus providing an electrode layer insulated and spaced apart from the working surface.
• In performing the method of the invention with the microchannel structure ofFIGS. 19A-19C, the neutral gas media m₂flows through theinterior passageway244 of the catheter body268, as described in the previous embodiment. As can be understood inFIG. 19C, the flow of media m₂through the microchannel structure displaces any surface fluids indicated at m₁from the mucosa. Next, the neutral media m₂is altered to a conductive or ionized media m₂′ by generating an intense electric field within the microchannel portions between the pairedelectrode layers235 and245 as depicted inFIG. 19D. In other words, field ionization means are utilized to ionize the gas volumes flowing within the microchannel structure. The ionized gas will thereafter remain conductive as it flows through the workingsurface215 thus creating the conductive media volumes v, the same as depicted inFIGS. 15C-15E. The conductivity of the gas volumes v within and about the open microchannel terminations222a-222z(cf.FIG. 15D) can thus be ionized and deionized in rapid intervals (as described above with photoionization) by rapid on/off modulation of the intense electric field (e.g., ranging from 200 to 5000 volts) between pairedelectrode layers235 and245 to achieve pulsed energy applications and micro-scale ablations as depicted inFIG. 15E. It is believed that by providing an independent means (first energy source atelectrodes235 and245) for switching the media between conductive and non-conductive at a selected high repetition rate, the invention will provide precise control over the brief intervals in which the energy-tissue interactions eti occur, rather than the uncontrolled intervals which would occur if high intensity current were delivered toelectrode layer225 alone to cause random time intervals of ionization and electrical discharge across the gas volumes. As shown inFIG. 19A, the working end can be translated across the mucosal lining mu under endoscopic vision to ablate very thin cell layers substantially without collateral thermal damage to deeper tissue layers.
• VI. Construction of Exemplary Type De “D” System for Plasma-Assisted Material Removal.
• The previous sections described application of high intensity electrical energy to cause volumetric removal of tissue layers (i) in a pulsed high intensity mode for creating micron dimensioned discrete energy-tissue interactions to ablate tissue, or (ii) in the creation of a continuously sustained layer of high energy microplasmas about the working surface of the instrument to cause true plasma-mediated molecular volatilization of surface macromolecules to remove tissue volume. The Type “D” system described next functions almost identically to plasma-mediated system described previously, with the exception that the electrode arrangement of the working surface is adapted to insure that maximal average voltage is applied to the ionized gas volumes v continuously (cfFIG. 15D), rather than in intervals that vary with current frequency.
• A portion of the Type “D” workingsurface315 and microchannel structure is shown inFIG. 20 with the novel electrode arrangement that comprises at least two spaced apart electrode layers325aand325binstead of one electrode layer (e.g.,electrode layer225 of the Type “C” embodiment ofFIGS. 11-12). The scope of the invention includes anywhere from 2 to about 4 electrode layers and for clarity, the invention is described with two such electrode layers.FIG. 20 shows anexemplary working surface315 and twoelectrode layers325aand325bwith exposedsurfaces327aand327bin the microchannels320 (collectively). These two electrode layers are separate from the MCP electrode layers235 and245 that are the same as previously described. Each of the electrode layers325aand325bis coupled to theelectrical source60 andcontroller45 by a separate lead329aand329b.Of particular interest, theelectrical source60 is capable of generating overlapping waveforms of the voltage delivered to eachelectrode layer325aand325b,by which in meant that the energy delivered to each electrode's frequency is out of phase with the other, depicted as Phase A and Phase B inFIG. 20. In a system with twosuch electrode layers325aand325b,the phase of the waveforms would be shifted by about ½ the frequency of the waveform; in a system with three such electrode layers325a-325c(not shown) the phase of the waveforms would be shifted by about ⅓ the frequency, etc. Anelectrical source60 can be adapted with circuitry known in the art to deliver such out-of-phase voltage waveforms to the spaced apart electrodes.
• In general, it is postulated that such a system with spaced apart electrode layers325aand325bwill cooperate with areturn electrode85 to maintain high voltage energy delivery to microplasma volumes v formed about the opendistal terminations322 of microchannels to insure a continuous high energy plasma for causing molecular volatilization of the surface molecules at the targeted site ts. In the operation of the previous Type “C” embodiment, the electric field between theelectrode225 and returnelectrode85 would diminish in intensity depending of the voltage waveform as voltage difference between theactive electrode225 and thereturn electrode85 varied. In this embodiment, an additional voltage differential would occur at certain intervals of the selected frequency between the out-of-phase voltages at the electrode layers325aand325b,in addition to the field created between these electrode layers and thereturn electrode85. Thus, a method of the invention relating to the Type “D” system comprises (i) providing at least two closely spaced electrodes that have overlapping or out-of-phase voltage waveforms in an instrument working surface, in addition to a return electrode that cooperates with the working surface in contact with the targeted site ts or on the spaced apart portion of the instrument working end, (ii) creating and transiently capturing (by any suitable bubble creation means) a neutral gas volume that engages the at least two out-of-phase electrodes and further engages the targeted site ts; (iii) delivering intense energy to the electrode arrangement (e.g., in frequency range of about 250 kHz to 3.5 MHz) to sustainably ionized the transient gas volumes at high energy levels sufficient to cause volumetric removal of the surface layers of the targeted site ts.
• FIG. 21 generalizes the invention insofar as it relates to the utilization of multiple, closely spaced, overlappingphase electrodes325aand325bin a multiple adjacent recessed channel or chamber portions388a-88chaving the above-described micron dimensions in a workingsurface390 that does not provide an independent means for introducing neutral gas volumes to the working surface. In other words, the invention may be used with high-intensity energy delivery (described above) to vaporize insulative bubbles from a fluid on, or within, the targeted tissue surface and to thereafter cause an intense energy discharge across the bubble to ablate tissue. The micron dimensions of the features of such a workingsurface390 in combination with the out-of-phase energy applications to multiple electrodes provides a novel modality of tissue ablation, wherein the intensity of energy delivery across the expanding and collapsing bubbles is enhanced by the higher average voltages over a selected time interval to cause limited collateral thermal damage.
• VII. Construction of Exemplary Type “E” System for Energy Application
• FIGS. 22A-22B below illustrate a Type “E” embodiment400 that provides an additional energy delivery mode that has been found to optimize the formation, character and dimension of gas bubbles in the interface between the working surface415 and the targeted tissue.
• More in particular, it has been found the application of vibrational energy to, and about, the working surface can increase the efficiency of the electrical energy application across the transient gas volume or bubbles that are formed between the working surface and the targeted tissue. In one embodiment, referring toFIG. 22, the instrument body410 extends to a working surface415 that, for convenience shows a single media entrance channel422 but a plurality of microchannel entrance ports are more practical for a typical dimension working end as shown inFIGS. 12, 13,19C,19C and20. A remote source of a selected gas as described previously is operatively coupled to the instrument to provide flow through the at least one single media entrance channel422 to the working surface.
• The embodiment ofFIG. 22A further shows that a vibration source430 is operatively coupled to the instrument body410. The scope of the invention includes any vibration source and preferably is any ultrasonic transducer known in the art that can couple acoustic energy to the instrument body410. One type of ultrasonic transmission system can provide a proximal body portion (not shown) of the instrument (a transducer portion) that comprises at least one piezoelectric element together with opposing polarity electrodes coupled to each such element. The piezoelectric elements can be fabricated of a suitable material, e.g., lead zirconate-titanate, or any other piezoelectric material. In use, the piezoelectric elements convert an electrical signal into mechanical energy that results in a longitudinal vibratory motion in a shaft portion of the instrument body to deliver such energy to the working surface415. Such an ultrasonic transmission unit is tuned acoustically as is known in the art to provide that the selected longitudinal vibration frequency that can be effective in vibrating the gas introduced through the at least one channel. In one embodiment, the gas is introduced through the working end surface through a plurality of channels having a cross-section of leas than about 1 micron. More preferably, the channels have a cross-section of less than about 0.5 microns. State another way, the channels preferably are of a selected dimension that is too small to allow inflow of fluid—but will still allow gas flow therethrough. Such a dimension will insure that a gas volume is trapped about the opening of each channel termination for energy delivery thereacross.
• When the above described ultrasonic assembly is energized, a vibratory motion in the form of a standing wave is generated throughout the length of the instrument body410. The propagation of such vibratory motion at particular points along the length of the instrument body410 depends on the exact longitudinal location at which the vibratory motion is measured. A minimum in the vibratory motion or standing wave is commonly referred to as a node, wherein motion is at minimal level. The location at which the vibratory motion reaches a peak in the standing wave is referred to as an anti-node, and the length of the instrument body410 is selected to provide an anti-node characteristics generally at the working surface415 to deliver a maximum amount of energy thereto. Any suitable electrical source and controller can be coupled to the piezoelectric elements to drive or excite the ultrasonic assembly at any suitable resonant frequency of the tuned acoustic assembly.
• In operation, the piezoelectric elements are energized in response to an electrical signal provided by source to thereby produce an acoustic standing wave in the instrument body contemporaneous with the introduction of a selected gas to the working surface (seeFIG. 22A-22B). The delivery of the acoustic energy alters the characteristic of the gas volume transiently captured between the working surface and the targeted tissue. The acoustic energy application has been found to be useful for lowering the power or voltage requirements to apply ablative energy across the gas interface between working surface415 and the targeted tissue, for example in the fluid environment ofFIGS. 22A-22B. Without wishing to be limited to any particular theory to explain the reasons for the increases effectiveness of the energy application, it is believed that the acoustic energy alters or diminishes the surface tension of the gas volume(s) or bubbles in the fluid environment, fragments the gas bubble(s) into smaller dimensions, detaches the gas bubbles from the working surface, or in general, very rapidly creates a more refined gas volume between the working surface and the targeted tissue. By this means, the voltage required to cause an ablative electrical discharge across the introduced gas is lessened.
• The vibrational or acoustic energy as described above can be applied in a continuous manner to the working end, or it can be applied in a pulsed manner. The scope of the invention includes the use of such vibrational energy in any electrosurgical working end that is adapted to apply energy to tissue, and in particular to such instruments that are adapted to apply energy for purposes of ablation or volumetric removal as described above. The types of instrument working ends that fall within the scope of the invention includes, but is not limited to, probe working ends for applying energy to tissue in procedures in orthopedics, endovascular interventions, neurointerventions, ENT, urology and general surgery. The invention also may be used in the jaws of grasping-type instruments. The vibrational energy can be combined with the instruments described above that use photoionization of the gas volume, or the vibrational energy can be used independently thereof—still in combination with the electrical energy application components described above.
• In another embodiment shown inFIG. 23, theprobe working end500 can use ultrasound energy at the workingsurface515 to create cavitation bubbles to provide an interface between the working surface and the targeted tissue. Such cavitation bubbles can causes by an intense energy application of energy to a targeted media. When absorption of energy by the target media results in thermoelastic expansion of the target and a rise in internal pressures within the target. The term stress confinement refers to the process of causing an increase in pressure within a targeted media before the pressure can dissipate from the target at the speed of sound. When there exists a defined or free boundary between the targeted media and different surrounding media—such as a liquid or gas interface with the target—the target expands at its surface and then snaps back. The expansion phase is positive pressure or stress and the snap-back is negative stress. When the negative stress exceeds the strength of target media, that media breaks, disintegrates or ejects a surface portion thereof For example, an intense energy application whether from an electrical source, laser source or acoustic (mechanical) source can induce from 100° to 1000° C. temperature rises in a targeted composition and thereby can cause transient pressures of from 100-1000 atmospheres to explode the targeted composition. The same process of energy deposition in a targeted media can cause the formation of a bipolar positive/negative stress wave that propagates into surrounding media. If the surrounding media were a substantially solid material, the stress wave causes a fracture or break in the material called a spall plane. If the surrounding media were a liquid or a soft tissue, the bi-polar positive/negative stress wave would create cavitation bubbles in the media. In a liquid such as water, when absorbing energy in an intense manner, even a slight 5° to 20° C. temperature rise within a nanosecond or microsecond energy application interval can yield a ±10 atm (atmosphere) bipolar stress wave—and the −10 atm negative stress can cause cavitation in water. Thus, the invention can use ultrasound energy as is known in the art to create such cavitation bubbles (either in a continuous mode or pulsed mode).
• The scope of the invention includes the application of acoustic energy to create cavitation bubbles in a fluid media about the working surface of the probe. Thereafter, the invention includes the application of electrical energy across the environment of expanding and collapsing cavitation bubbles to ablate tissue. This type of probe does not need a gas inflow source of the previous embodiments, since the acoustic cavitation system provides the desired interface between the workingsurface515 and the targeted tissue. This type of working end can be used with or without the photoionization method and apparatus described in previous embodiments.
• While the plasma-assisted energy delivery methods above have been described in connection with several surgical procedures for volumetric tissue removal, such as skin resurfacing, the ablation of pre-cancerous or malignant cell layers and in spine surgery, it will be clear to those having skill in the art that the system has operational characteristics that may be suitable for a wide range of volumetric tissue removal procedures in, or on, structure of a patient's body. The system and method of the invention are suitable for other arthroscopic surgeries, including partial meniscectomies, synovectomies, chondroplasties, tendon and cartilage removals, and in general resurfacing and texturing of cartilage, tendon and bone surfaces. In addition, in the ENT and GI fields, there are a variety of procedures that require volumetric tissue removal either at a tissue surface or at the end of a probe inserted percutaneously in treating nose and throat disorders, for example, soft palate volume reduction surgery, turbinate reduction surgery and jaw bone surgery. These procedures require that the surgeon be provided with means to remove tissue in close proximity to delicate structures and nerves that cannot be damaged, which procedures lend themselves to the methods disclosed herein. In many fields, the selective removal of malignant tissue or other tumors may be accomplished by the present invention. For example, a form of stereotactic-directed probe may be used to ablate breast lesions. The method of the invention also may have use in interventional cardiology to remove vascular occlusions. The method of the invention also may be useful for drilling holes in tissue such as in TMR procedures (transmyocardial revascularization). The material removal methods described above apply to all body structures, which include non-anatomic structures such as accretions, calculi and the like.
• Those skilled in the art will appreciate that the exemplary embodiments and descriptions thereof are merely illustrative of the invention as a whole, and that variations in controlling the duration of intervals of energy delivery, in controlling the repetition rate, and in controlling the voltage applied to create the interval of intense electric fields may be made within the spirit and scope of the invention. Accordingly, the present invention is not limited to the specific embodiments described herein, but includes the features disclosed in the author's co-pending applications listed in the Section above titled “CROSS-REFERENCE TO RELATED APPLICATIONS” and the invention is defined by the scope of the appended claims. Specific features of the invention may be shown in some figures and not in others, and this is for convenience only and any feature may be combined with another in accordance with the invention. While the principles of the invention have been made clear in the exemplary embodiments, it will be obvious to those skilled in the art that modifications of the structure, arrangement, proportions, elements, and materials may be utilized in the practice of the invention, and otherwise, which are particularly adapted to specific environments and operative requirements without departing from the principles of the invention. The appended claims are intended to cover and embrace any and all such modifications, with the limits only of the true purview, spirit and scope of the invention.

Claims (15)

1. A medical device for delivering energy to targeted tissue, comprising:

an elongated member having a distal working end;

an interior flow channel having a first cross-section, the flow channel transitioning to at least one channel portion having a second smaller cross-section and terminating in at least one outlet in the distal working end;

at least one electrode element carried in said working end; and

a conductive flow media source for providing a flow through the interior flow channel, and wherein the electrical energy delivery to the flow proximate the at last one outlet creates a plasma for ablation of tissue.

2. The medical device ofclaim 1 further comprising a vibration source coupled to the elongated member.

3. The medical device ofclaim 1 further comprising a vibration source coupled to the working end.

4. The medical device ofclaim 1 wherein the at least one channel portion comprises one substantially linear channel.

5. The medical device ofclaim 1 wherein the at least one channel portion comprises a plurality of substantially linear channels.

6. The medical device ofclaim 1 wherein the at least one channel portion comprises a microporous structure.

7. The medical device ofclaim 1 wherein the working end is a ceramic.

8. The medical device ofclaim 1 wherein the at least one channel portion has a mean cross section across a principal axis of less than about 1000 microns.

9. The medical device ofclaim 1 wherein the at least one channel portion has a mean cross section across a principal axis of less than about 500 microns.

10. The medical device ofclaim 1 wherein the at least one channel portion has a mean cross section across a principal axis of less than about 250 microns.

11. The medical device ofclaim 1 wherein the flow media comprises saline solution.

12. The medical device ofclaim 1 wherein the flow media comprises hypertonic saline solution.

13. The medical device ofclaim 1 further including first and second polarity electrical terminals for coupled electrical energy to the flow media.

14. The medical device ofclaim 13 wherein the first polarity electrical terminal is within the interior channel.

15. The medical device ofclaim 13 wherein the first polarity electrical terminal is within the on an exterior of the working end.

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