WO1998007468A1 - Apparatus for treating chondromalicia - Google Patents

Apparatus for treating chondromalicia Download PDF

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Publication number
WO1998007468A1
WO1998007468A1 PCT/US1997/013044 US9713044W WO9807468A1 WO 1998007468 A1 WO1998007468 A1 WO 1998007468A1 US 9713044 W US9713044 W US 9713044W WO 9807468 A1 WO9807468 A1 WO 9807468A1
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WO
WIPO (PCT)
Prior art keywords
thermal energy
cartilage
energy delivery
fibrillated
distal end
Prior art date
Application number
PCT/US1997/013044
Other languages
French (fr)
Inventor
Gary Fanton
Hugh Sharkey
Original Assignee
Oratec Interventions, Inc.
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Oratec Interventions, Inc. filed Critical Oratec Interventions, Inc.
Priority to AU38133/97A priority Critical patent/AU3813397A/en
Publication of WO1998007468A1 publication Critical patent/WO1998007468A1/en

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Classifications

    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61N—ELECTROTHERAPY; MAGNETOTHERAPY; RADIATION THERAPY; ULTRASOUND THERAPY
    • A61N7/00—Ultrasound therapy
    • A61N7/02—Localised ultrasound hyperthermia
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B17/00—Surgical instruments, devices or methods, e.g. tourniquets
    • A61B17/32—Surgical cutting instruments
    • A61B17/320016—Endoscopic cutting instruments, e.g. arthroscopes, resectoscopes
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B18/00—Surgical instruments, devices or methods for transferring non-mechanical forms of energy to or from the body
    • A61B18/04—Surgical instruments, devices or methods for transferring non-mechanical forms of energy to or from the body by heating
    • A61B18/12—Surgical instruments, devices or methods for transferring non-mechanical forms of energy to or from the body by heating by passing a current through the tissue to be heated, e.g. high-frequency current
    • A61B18/14—Probes or electrodes therefor
    • A61B18/148—Probes or electrodes therefor having a short, rigid shaft for accessing the inner body transcutaneously, e.g. for neurosurgery or arthroscopy
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61N—ELECTROTHERAPY; MAGNETOTHERAPY; RADIATION THERAPY; ULTRASOUND THERAPY
    • A61N1/00—Electrotherapy; Circuits therefor
    • A61N1/40—Applying electric fields by inductive or capacitive coupling ; Applying radio-frequency signals
    • A61N1/403—Applying electric fields by inductive or capacitive coupling ; Applying radio-frequency signals for thermotherapy, e.g. hyperthermia
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B17/00—Surgical instruments, devices or methods, e.g. tourniquets
    • A61B17/32—Surgical cutting instruments
    • A61B17/3203—Fluid jet cutting instruments
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B18/00—Surgical instruments, devices or methods for transferring non-mechanical forms of energy to or from the body
    • A61B18/04—Surgical instruments, devices or methods for transferring non-mechanical forms of energy to or from the body by heating
    • A61B18/12—Surgical instruments, devices or methods for transferring non-mechanical forms of energy to or from the body by heating by passing a current through the tissue to be heated, e.g. high-frequency current
    • A61B18/14—Probes or electrodes therefor
    • A61B18/1442—Probes having pivoting end effectors, e.g. forceps
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B17/00—Surgical instruments, devices or methods, e.g. tourniquets
    • A61B17/32—Surgical cutting instruments
    • A61B17/320068—Surgical cutting instruments using mechanical vibrations, e.g. ultrasonic
    • A61B2017/320072—Working tips with special features, e.g. extending parts
    • A61B2017/320078—Tissue manipulating surface
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B18/00—Surgical instruments, devices or methods for transferring non-mechanical forms of energy to or from the body
    • A61B18/04—Surgical instruments, devices or methods for transferring non-mechanical forms of energy to or from the body by heating
    • A61B18/12—Surgical instruments, devices or methods for transferring non-mechanical forms of energy to or from the body by heating by passing a current through the tissue to be heated, e.g. high-frequency current
    • A61B18/1206—Generators therefor
    • A61B2018/1246—Generators therefor characterised by the output polarity
    • A61B2018/126—Generators therefor characterised by the output polarity bipolar

Definitions

  • This invention relates generally to a method and apparatus for treating chondromalacia, and more particularly to a method and apparatus that treats chondromalacia with minimal disruption of the cartilage bed of the knee
  • Normal articular cartilage consists of an assembly of large and small proteoglycans, collagens, hyaluronic acid and glycoproteins These matrix macromolecuies originate from chondrocytes localized in a nonrandom pattern through the cartilage matrix In normal joints, chondrocytes do not proliferate, dividing chondrocytes indicate a change in cartilage homeostasis, either as regeneration or attempted repair Chondromalacia occurs when cartilage beds in joints become worn and strands of cartilage distended away from their respective cartilage beds and extend into the joint capsule The cartilage surface becomes visibly disrupted, fissured and fibrillated This has dete ⁇ ous effects on the mechanical properties of articular cartilage This distension has been associated with knee pain Treatment to date has included surgical intervention In one arthroscopic procedure, a shaver is introduced through an arthroscope and is used to remove the strands of disrupted and fibrillated cartilage However, this treatment can disrupt and remove part of the normal cartilage bed and does
  • an object of the invention is to provide a method and apparatus for treating fibrillated or irregular cartilage joint surfaces
  • Another object of the invention is to provide a method and apparatus for delivering sufficient thermal energy to reduce a level of fibrillation of a fibrillated cartilage joint surface
  • Yet another object of the invention is to provide a method and apparatus for delivering sufficient thermal energy to modify a fibrillated cartilage joint surface to a smooth surface
  • a further object of the invention is to provide a method and apparatus for delivering sufficient thermal energy to modify an irregular cartilage joint surface to a smoother surface
  • Still a further object of the invention is to provide a method and apparatus for delivering sufficient thermal energy to at least a portion of a plurality of cartilage strands coupled to a fibrillated cartilage surface, and melt the strands onto the fibrillated cartilage surface.
  • Another object of the invention is to provide a method and apparatus that uses thermal energy to treat chondromalacia
  • a thermal delivery apparatus that has a probe means including a distal end and a proximal end
  • a first electrode means is positioned at the distal end of the probe means
  • the first electrode means is configured to deliver sufficient thermal energy to a fibnllated cartilage surface to reduce a level of fibrillation of the fibrillated cartilage surface
  • a cabling means is coupled to the proximal end of the probe means
  • an apparatus is configured to be positioned adjacent to a fibrillated cartilage joint surface
  • a probe means has a distal end and a proximal end
  • An insulator means has a first surface and a second surface
  • a first electrode means is positioned on the first surface of the insulator
  • the first electrode means has a first thermal energy delivery surface configured to deliver sufficient thermal energy to a plurality of cartilage strands coupled to the fibrillated cartilage joint surface to reduce a level of fibrillation of surface
  • a second electrode means is positioned on the second surface of the insulator
  • a cable means is coupled to the proximal end of the probe means
  • a method modifies a geometry of a fibrillated cartilage surface
  • a thermal energy delivery device is provided and includes a probe means with a distal end and a thermal energy delivery surface
  • a thermal energy source is also provided and coupled to the thermal energy delivery surface The thermal energy delivery surface is positioned adjacent to the fibnllated cartilage surface in a non-contacting position Sufficient
  • the apparatus of the present invention may also include a sensor means positioned at the distal end of the probe means
  • a comparator means is provided and compares a measured temperature value at the sensor means with a predetermined temperature value The comparator means generates a disabling signal if the measured temperature value exceeds the predetermined maximum temperature value
  • a communication means is provided and communicates the disabling signal to the thermal energy source means to cease further delivery of energy from the thermal energy source means to the first electrode means.
  • sufficient thermal energy is delivered from the thermal energy delivery surface to modify the fibrillated cartilage surface to a smooth surface
  • Thermal energy is delivered from the thermal energy delivery surface to create a less fibrillated, fibrillated cartilage surface
  • Thermal energy is delivered from the thermal energy delivery surface to cause at least a portion of a plurality of cartilage strands coupled to the fibrillated cartilage surface to create a smoothened cartilage surface
  • Thermal energy is delivered from the thermal energy delivery surface to cause at least a portion of a plurality of cartilage strands coupled to the fibrillated
  • FIGURE 1 is a perspective view of the apparatus of the present invention with a probe and two electrodes
  • Figure 2 is a perspective view of the apparatus of the present invention with a probe, an electrode positioned at a distal end of the probe and two electrodes positioned on opposite sides of an insulator
  • Figure 3 is a perspective view of a knee joint with chondromalacia.
  • Figure 4 is a perspective view of the apparatus of Figure 2 with a probe coiled distal end
  • Figure 5 is a perspective view of the apparatus of the present invention with two electrodes positioned on opposite sides of an insulator
  • Figure 6 is perspective view of the apparatus of the present invention including an electrode with radiused edges
  • Figure 7 is a perspective view of the apparatus of the present invention including a rectangularly shaped electrode.
  • Figure 8 illustrates a perspective view of the apparatus of the present invention with electrodes formed on peripheral faces of the insulator
  • Figure 9 is a cross-sectional view of the apparatus of Figure 8 taken along the lines 9-9
  • Figure 10 is a perspective view of an electrode used with the apparatus of the present invention that is formed at a peripheral surface of the insulator and defines an interior non-conducting region.
  • Figure 1 1 is a perspective view of a toroidal electrode used with the apparatus of the present invention and defines an interior non-conducting region.
  • Figure 12 is a perspective view of a non-circular toroidal electrode used with the apparatus of the present invention and defines an interior nonconducting region
  • Figure 13 is a perspective view of a segmented electrode used with the apparatus of the present invention.
  • Figure 14 is a perspective view of a segmented toroidal electrode used with the apparatus of the present invention.
  • Figure 15 is a perspective view of a flexible probe used with the apparatus of the present invention.
  • Figure 16 is a block diagram illustrating a feedback system useful to control the temperature of electrodes of the present invention.
  • Figure 17 illustrates a circuit useful to implement the feedback system of Figure 16.
  • a thermal energy delivery apparatus 10 is configured to be positioned adjacent to, but spaced apart from a joint surface. Included is a probe 12 with a distal end 14, a first electrode 22 and a second electrode 24. Electrodes 22 and 24 can be operated in bipolar or monopolar Bipolar is preferred A distancing element 25 distances a thermal energy deliven, surface of electrode 22 from the joint surface Preferably, the thermal energy delivery surface of electrode 22, or of electrode 24, does not touch the joint surface As illustrated in Figure 1 , distancing element 25 is included In other embodiments, distancing element 25 is not included and the thermal energy delivery surface of electrode 22 or of electrode 24 are positioned directly on the joint surface
  • thermal energy delivery apparatus 10 is configured to be positioned and deliver thermal energy to a joint surface
  • Apparatus 10 includes probe 12 with distal end 14 and an insulator 16 including first and second surfaces 18 and 20 formed on opposite sides on insulator 16 A pair of electrodes are also provided
  • First electrode 22 is positioned on first surface 18 of insulator 16
  • Second electrode 24 is positioned on second surface 20 of insulator 16
  • Thermal energy source 26 is coupled to first electrode 22 and second electrode 24 with a cable
  • Insulator 16 can be an elongated structure with a longitudinal axis
  • Surfaces 18 and 20 can be parallel to each other Insulator can be made of a variety of insulating materials known to those skilled in the art Insulator 16 need not be one integral unit and surfaces 18 and 20 can be made of separate insulators that are separated Surfaces 18 and 20 can be planar, non-planar and have geometries that conform closely to inte ⁇ or joint surfaces In one embodiment, the dimensions of distal end 14 are sufficiently small to be positioned on a joint surface
  • Knee joint surface 28 is defined by a first cartilage bed 30 formed at a distal end of the femur, and a second cartilage bed 32 formed at a distal end of the tibia
  • the present invention is not limited to the knee joint surface and can be used in a variety of different joint surfaces Any joint surface susceptible to chondromalacia is treatable with apparatus 10
  • the present invention is suitable for the treatment of fibnllated cartilage joint surfaces to reduce the level of fibrillation and create smoother surfaces.
  • the present invention is also used to treat irregular joint surfaces, where there are peaks and valleys, and create a less irregular joint surface. In certain embodiments, the irregular joint surface becomes a smooth joint surface.
  • a first plurality of cartilage strands 34 are coupled to first cartilage bed 30 and have become dislodged and dangle in joint surface 28.
  • a second plurality of cartilage strands 36 are connected to second cartilage bed 32. Second plurality of cartilage strands 36 have also become dislodged and dangle in joint surface 28.
  • a method modifies a geometry of a fibrillated cartilage surface.
  • Sufficient thermal energy is delivered from first electrode 22 or second electrode 24 at different times to reduce a level of fibrillation of the fibrillated cartilage joint surface.
  • sufficient thermal energy is delivered electrode 22 or 24 to, (i) change the fibrillated cartilage surface to a smooth or smoother surface, (ii) reduce a level of fibrillation of the fibrillated cartilage surface, (iii) cause at least a portion of a plurality of cartilage strands coupled to the fibrillated cartilage surface to create a smoothened cartilage surface, (iv) cause at least a portion of a plurality of cartilage strands coupled to the fibrillated cartilage surface to melt onto the fibrillated cartilage surface or (v) melt at least a portion of a plurality of cartilage strands to create a smoothened cartilage surface.
  • First electrode 22 has a first thermal energy delivery surface configured to deliver thermal energy to cartilage strands 34 and second electrode 24 has a second thermal energy delivery surface configured to deliver thermal energy to cartilage strands 36.
  • Thermal energy includes but is not limited to RF, microwave, resistive heating, ultrasound, coherent or incoherent light and a thermal jet source.
  • RECTIFIED SHEET (RULE 91) ISA/EP of cartilage beds 30 and 32, changes the ultrastructure of the cartilage, stimulates cartilage replication and growth and changes the chemical environment in joint surface 28 and cartilage beds 30 and 32 to relieve pain
  • Apparatus 10 is used to modify the geometry of cartilage strands 34 and 36 through cartilage shnnkage and possibly limited ablation of strands 34 and 36
  • Distal end 14 of probe 12 is inserted through an arthroscope to joint surface 28
  • First and second electrodes 22 and 24 are introduced into joint surface 28
  • Sufficient thermal energy is delivered from electrodes 22 and 24 to shnnk at least a portion of cartilage strands 34 and 36, causing the strands to e down on cartilage beds 30 and 32
  • the delivery of thermal energy to joint surface 28 results in an "ironing" of cartilage strands 34 and 36 onto cartilage beds 30 and 32
  • Sufficient thermal energy is delivered from first and second electrodes 22 and 24 to shrink at least a portion of cartilage strands 34 and 36 without ablating more than 25% of cartilage beds 30 and 32
  • sufficient energy is delivered by first and second electrodes 22 and 24 to raise the temperature of joint surface in the range of 45 to 90 degrees C, preferably 45 to 75 degrees C and more preferably 50 to 70 degrees C
  • Maintenance of a suitable temperature, and the delivery of thermal energy to joint surface 28, is sufficient to cause strands 34 and 36 to become at least partially melted onto the cartilage joint surface while minimizing ablation of cartilage beds 30 and 32
  • Insulator 26 and first and second electrodes 22 and 24 are configured to be inserted into joint surface 28
  • Probe 12 is moved back and forth through joint surface 28 to deliver a sufficient amount of thermal energy to strands 34 and 36 to cause them to lie down on their respective cartilage beds
  • the thermal energy delivery surfaces of first and second electrodes 22 and 24 can move along the surfaces of cartilage beds 30 and 32 to complete the ironing effect
  • distal end 14 of probe 12 can have a coiled geometry as well as a variety of geometric configurations
  • distal end 14 is malleable or sufficiently flexible to impart movement of first and second electrodes 22 and 24
  • Distal end 14 can pivot, be hinged, be articulated, or made of a shaped memory metal, and the like, in order to enable first and second electrodes 22 and 24 to follow the contours of joint surface 28
  • first and second electrodes 22 and 24 can be operated in a bipolar mode This concentrates the flow of RF energy between first and second electrodes 22 and 24 and diverts direct RF energy flow away from cartilage beds 30 and 32 RF energy which is directed between first and second electrodes 22 and 24 heats up fluids within joint surface 28 and provides a more controlled delivery of energy to cartilage strands 34 and 36 RF ablation of cartilage beds 30 and 32 is reduced
  • First and second electrodes 22 and 24 can have a vanety of different geometric configurations As illustrated in Figure 6.
  • first and second electrodes 22 and 24 are symmetrically shaped with radiused edges Elimination of sharp edges at an electrode surface reduce the creation of hot spots of thermal energy delivered to a site
  • first and second electrodes 22 and 24 have rectangular geometries with non-radiused edges
  • First and second electrodes 22 and 24 can each have different sizes and geometries
  • First and second electrodes 22 and 24 can be mirror images of each other or they can be different
  • first and second electrodes 22 and 24 are formed on a periphery of insulation surfaces 18 and 20 respectively
  • each electrode 22 and 24 defines a first and a second nonconducting region 38 and 40 on an insulator surface 18 and 20 within an interior of first and second electrodes 18 and 20
  • Non-conducting regions 38 and 40 can be the actual surface of insulator 16, or may be additional structures, each with a non-conducting surface, that are formed on insulation surfaces 18 and 20
  • First and second sensors 42 and 44 can be provided and associated with first and second electrodes 22 and 24 to measure temperature and/or impedance First and second sensors 42 and 44 are positioned on a surface of first and second electrodes 22 and 24. on a surface of probe 12, on non-conducting regions 38 and 40, or can be advanced and retracted from distal end 14 to and from joint surface 28.
  • First and second sensors 42 and 44 are of conventional design, including but not limited to thermistors, thermocouples, resistive wires, and the like.
  • Suitable thermal sensors 42 and 44 include a T type thermocouple with copper constantene, J type, E type, K type, fiber optics, resistive wires, thermocouple IR detectors, and the like. Sensors 42 and 44 need not be thermal sensors.
  • Sensors 42 and 44 measure temperature and/or impedance to permit monitoring and a desired level of energy delivered determined This reduces ablation damage to cartilage beds 30 and 32. If at any time sensor 42 or 44 determines that a desired temperature is exceeded, then an appropriate feedback signal is received at thermal energy source 26 which then regulates the amount of energy delivered to first and second electrodes 22 and 24
  • Non-conducting regions 38 and 40 have a variety of geometric surfaces including but not limited to planar, non-planar, concave, convex, and the like. In one embodiment, non-conducting regions 38 and 40 are closer to the midline of insulator 16 than first and second electrodes 22 and 24. This enhances the bipolar conduction of thermal energy between electrodes 22 and 24 in the bipolar mode of operation.
  • First and second electrodes 22 and 24 can have various geometries including but not limited to cylindrical, semi-cylindrical, rectangular, cubic, irregularly shaped, toroidal (Figure 10), non-circular toroidal (Figure 1 1), non- symmetrical, non-symmetrical toroidal ( Figure 12) or be segmented and capable of multiplexing ( Figures 13 and 14).
  • first electrode 22 has a toroidal geometry
  • first sensor 42 is positioned on non-conducting region 38
  • distal end 14 is flexible and curved.
  • Figure 16 illustrates a block diagram of a temperature/impedance feedback system useful with apparatus 10. Thermal energy is delivered to first and second electrodes 22 and 24 by thermal energy source 26, and applied to
  • RECTIFIED SHEET (RULE 91) ISA/EP cartilage strands 34 and 36
  • a monitor 56 ascertains tissue impedance, based on the energy delivered to tissue, and compares the measured impedance value to a set vaiue If the measured impedance exceeds the set value a disabling signal 48 is transmitted to thermal energy source 26, ceasing further delivery of thermal 5 energy to first and second electrodes 22 and 24. If measured impedance is within acceptable limits, energy continues to be applied During the application of thermal energy to cartilage strands 34 and 36, sensor 42 measures the temperature at the surface of sensor 42 A comparator 50 receives a signal representative of the measured temperature and compares this value to a pre-set
  • signal representative of the desired temperature Comparator 50 sends a signal to thermal energy source 26 to continue sending thermal energy, to increase or decrease the level of delivered thermal energy, or to cease delivery of thermal energy
  • An output 52 from temperature comparator 50 can be input to thermal
  • thermal energy source 26 is coupled to first and second electrodes 22 and 24 and apply a biologically safe voltage to
  • apparatus 10 is represented as a bipolar ablation device
  • First and second electrodes 22 and 24 are connected to a primary side of transformer windings 58 and 60
  • the common primary windings 58 and 60 are magnetically coupled with a transformer core to secondary windings 58' and 60'
  • the primary windings 58 of the first transformer t couple the output voltage of apparatus 10 to the secondary windings 58'
  • the primary windings 60 of the second transformer t 2 couple the output current of ablation apparatus 10 to the secondary windings 60 *
  • Measuring circuits determine the root mean square (RMS) values or
  • the output voltage of the divider circuit D is presented at the positive (+) input terminal of comparator A.
  • a voltage source V 0 supplies a voltage across the variable resistor R.., thus allowing one to manually adjust the voltage presented at the negative input of comparator A.
  • This voltage represents a maximum impedance value beyond which power will not be applied to electrode 22 Specifically, once the tissue is heated to a temperature corresponding to an impedance value greater than the maximum cut-off impedance, thermal energy source 26 stops supplying energy to first and second electrodes 22 and 24.
  • Comparator A can be of any of a commercially available type that is able to control the amplitude or pulse width modulation of thermal energy source 26
  • the temperature within joint surface 28 can be controlled based on the tissue impedance, as represented by signal 62, or based on tissue temperature, as represented by signal 64.
  • the switch S is activated to allow the impedance signal 62 to enter the positive (+) input terminal of comparator A. This signal along with the reference voltage applied to the negative (-) input terminal actuates comparator A to produce an output signal.
  • tissue impedance will exceed a selected impedance value seen at the negative (-) input terminal, thereby generating disabling signal 48 to disable thermal energy source 26, ceasing the energy supplied to first and second electrodes 22 and 24.
  • the output signal of comparator A may either disable thermal energy source's 26 energy output, depending on the tissue temperature as reflected by its impedance.

Abstract

A thermal energy delivery apparatus (10) has a probe means (12) including a distal end and a proximal end. A first electrode means (22) is positioned at the distal end of the probe means. The first electrode (22) means is configured to deliver sufficient thermal energy to a fibrillated cartilage surface to reduce a level of fibrillation of the fibrillated cartilage surface. A cabling means is coupled to the proximal end of the probe means.

Description

APPARATUS FOR TREATING CHONDROMALICIA
BACKGROUND OF THE INVENTION Field of the Invention
This invention relates generally to a method and apparatus for treating chondromalacia, and more particularly to a method and apparatus that treats chondromalacia with minimal disruption of the cartilage bed of the knee
Description of Related Art
The normal function of joints in humans depends on the distπbution of relatively large forces across the body surfaces In diarthrodial joints the magnitude of the joint forces reaches levels four to seven times bodv weight
These forces applied to joints are dispersed by articular cartilage Cartilage function occurs via a highly organized extracellular matrix maintaining a fixed charge density and possessing a high affinity for water
Normal articular cartilage consists of an assembly of large and small proteoglycans, collagens, hyaluronic acid and glycoproteins These matrix macromolecuies originate from chondrocytes localized in a nonrandom pattern through the cartilage matrix In normal joints, chondrocytes do not proliferate, dividing chondrocytes indicate a change in cartilage homeostasis, either as regeneration or attempted repair Chondromalacia occurs when cartilage beds in joints become worn and strands of cartilage distended away from their respective cartilage beds and extend into the joint capsule The cartilage surface becomes visibly disrupted, fissured and fibrillated This has deteπous effects on the mechanical properties of articular cartilage This distension has been associated with knee pain Treatment to date has included surgical intervention In one arthroscopic procedure, a shaver is introduced through an arthroscope and is used to remove the strands of disrupted and fibrillated cartilage However, this treatment can disrupt and remove part of the normal cartilage bed and does not restore a smooth surface nor the mechanical function
It would be desirable to provide a method and apparatus treating fibrillated cartilage joint surfaces or irregular cartilage joint surfaces by delivering sufficient thermal energy to reduce a level of fibrillation or irregularity of the fibrillated cartilage joint surface or the irregular cartilage joint surface It would also be desirable to modify the fibrillated cartilage surface to a smooth surface It would be further desirable to treat chondromalacia by reducing a level of fibrillation or irregularity of a fibrillated or irregular cartilage joint surface
SUMMARY OF THE INVENTION Accordingly, an object of the invention is to provide a method and apparatus for treating fibrillated or irregular cartilage joint surfaces
Another object of the invention is to provide a method and apparatus for delivering sufficient thermal energy to reduce a level of fibrillation of a fibrillated cartilage joint surface
Yet another object of the invention is to provide a method and apparatus for delivering sufficient thermal energy to modify a fibrillated cartilage joint surface to a smooth surface A further object of the invention is to provide a method and apparatus for delivering sufficient thermal energy to modify an irregular cartilage joint surface to a smoother surface
Still a further object of the invention is to provide a method and apparatus for delivering sufficient thermal energy to at least a portion of a plurality of cartilage strands coupled to a fibrillated cartilage surface, and melt the strands onto the fibrillated cartilage surface.
Another object of the invention is to provide a method and apparatus that uses thermal energy to treat chondromalacia These and other objects of the invention are achieved in a thermal
Figure imgf000005_0001
delivery apparatus that has a probe means including a distal end and a proximal end A first electrode means is positioned at the distal end of the probe means The first electrode means is configured to deliver sufficient thermal energy to a fibnllated cartilage surface to reduce a level of fibrillation of the fibrillated cartilage surface A cabling means is coupled to the proximal end of the probe means
In one embodiment of the invention an apparatus is configured to be positioned adjacent to a fibrillated cartilage joint surface A probe means has a distal end and a proximal end An insulator means has a first surface and a second surface A first electrode means is positioned on the first surface of the insulator The first electrode means has a first thermal energy delivery surface configured to deliver sufficient thermal energy to a plurality of cartilage strands coupled to the fibrillated cartilage joint surface to reduce a level of fibrillation of surface A second electrode means is positioned on the second surface of the insulator A cable means is coupled to the proximal end of the probe means In another embodiment, a method modifies a geometry of a fibrillated cartilage surface A thermal energy delivery device is provided and includes a probe means with a distal end and a thermal energy delivery surface A thermal energy source is also provided and coupled to the thermal energy delivery surface The thermal energy delivery surface is positioned adjacent to the fibnllated cartilage surface in a non-contacting position Sufficient thermal energy is delivered from the thermal energy delivery surface to reduce a level of fibrillation of the fibnllated cartilage surface The method and apparatus of the present invention can also be used to decrease the level of irregularity of an irregular cartilage surface
The apparatus of the present invention may also include a sensor means positioned at the distal end of the probe means A comparator means is provided and compares a measured temperature value at the sensor means with a predetermined temperature value The comparator means generates a disabling signal if the measured temperature value exceeds the predetermined maximum temperature value A communication means is provided and communicates the disabling signal to the thermal energy source means to cease further delivery of energy from the thermal energy source means to the first electrode means In various embodiments of the invention, sufficient thermal energy is delivered from the thermal energy delivery surface to modify the fibrillated cartilage surface to a smooth surface Thermal energy is delivered from the thermal energy delivery surface to create a less fibrillated, fibrillated cartilage surface Thermal energy is delivered from the thermal energy delivery surface to cause at least a portion of a plurality of cartilage strands coupled to the fibrillated cartilage surface to create a smoothened cartilage surface Thermal energy is delivered from the thermal energy delivery surface to cause at least a portion of a plurality of cartilage strands coupled to the fibrillated cartilage surface to melt onto the fibrillated cartilage surface At least a portion of a plurality of cartilage strands are melted to create a smoothened cartilage surface
BRIEF DESCRIPTION OF THE FIGURES Figure 1 is a perspective view of the apparatus of the present invention with a probe and two electrodes
Figure 2 is a perspective view of the apparatus of the present invention with a probe, an electrode positioned at a distal end of the probe and two electrodes positioned on opposite sides of an insulator
Figure 3 is a perspective view of a knee joint with chondromalacia. Figure 4 is a perspective view of the apparatus of Figure 2 with a probe coiled distal end Figure 5 is a perspective view of the apparatus of the present invention with two electrodes positioned on opposite sides of an insulator
Figure 6 is perspective view of the apparatus of the present invention including an electrode with radiused edges Figure 7 is a perspective view of the apparatus of the present invention including a rectangularly shaped electrode.
Figure 8 illustrates a perspective view of the apparatus of the present invention with electrodes formed on peripheral faces of the insulator Figure 9 is a cross-sectional view of the apparatus of Figure 8 taken along the lines 9-9
Figure 10 is a perspective view of an electrode used with the apparatus of the present invention that is formed at a peripheral surface of the insulator and defines an interior non-conducting region. Figure 1 1 is a perspective view of a toroidal electrode used with the apparatus of the present invention and defines an interior non-conducting region.
Figure 12 is a perspective view of a non-circular toroidal electrode used with the apparatus of the present invention and defines an interior nonconducting region Figure 13 is a perspective view of a segmented electrode used with the apparatus of the present invention.
Figure 14 is a perspective view of a segmented toroidal electrode used with the apparatus of the present invention.
Figure 15 is a perspective view of a flexible probe used with the apparatus of the present invention.
Figure 16 is a block diagram illustrating a feedback system useful to control the temperature of electrodes of the present invention.
Figure 17 illustrates a circuit useful to implement the feedback system of Figure 16.
DETAILED DESCRIPTION
As shown in Figure 1, a thermal energy delivery apparatus 10 is configured to be positioned adjacent to, but spaced apart from a joint surface. Included is a probe 12 with a distal end 14, a first electrode 22 and a second electrode 24. Electrodes 22 and 24 can be operated in bipolar or monopolar Bipolar is preferred A distancing element 25 distances a thermal energy deliven, surface of electrode 22 from the joint surface Preferably, the thermal energy delivery surface of electrode 22, or of electrode 24, does not touch the joint surface As illustrated in Figure 1 , distancing element 25 is included In other embodiments, distancing element 25 is not included and the thermal energy delivery surface of electrode 22 or of electrode 24 are positioned directly on the joint surface
Referring now to Figure 2, thermal energy delivery apparatus 10 is configured to be positioned and deliver thermal energy to a joint surface Apparatus 10 includes probe 12 with distal end 14 and an insulator 16 including first and second surfaces 18 and 20 formed on opposite sides on insulator 16 A pair of electrodes are also provided First electrode 22 is positioned on first surface 18 of insulator 16 Second electrode 24 is positioned on second surface 20 of insulator 16 Thermal energy source 26 is coupled to first electrode 22 and second electrode 24 with a cable
Insulator 16 can be an elongated structure with a longitudinal axis Surfaces 18 and 20 can be parallel to each other Insulator can be made of a variety of insulating materials known to those skilled in the art Insulator 16 need not be one integral unit and surfaces 18 and 20 can be made of separate insulators that are separated Surfaces 18 and 20 can be planar, non-planar and have geometries that conform closely to inteπor joint surfaces In one embodiment, the dimensions of distal end 14 are sufficiently small to be positioned on a joint surface
A knee joint surface 28 is shown in Figure 3 Knee joint surface 28 is defined by a first cartilage bed 30 formed at a distal end of the femur, and a second cartilage bed 32 formed at a distal end of the tibia The present invention is not limited to the knee joint surface and can be used in a variety of different joint surfaces Any joint surface susceptible to chondromalacia is treatable with apparatus 10 The present invention is suitable for the treatment of fibnllated cartilage joint surfaces to reduce the level of fibrillation and create smoother surfaces. The present invention is also used to treat irregular joint surfaces, where there are peaks and valleys, and create a less irregular joint surface. In certain embodiments, the irregular joint surface becomes a smooth joint surface.
A first plurality of cartilage strands 34 are coupled to first cartilage bed 30 and have become dislodged and dangle in joint surface 28. A second plurality of cartilage strands 36 are connected to second cartilage bed 32. Second plurality of cartilage strands 36 have also become dislodged and dangle in joint surface 28.
In one embodiment of the invention, a method is provided that modifies a geometry of a fibrillated cartilage surface. Sufficient thermal energy is delivered from first electrode 22 or second electrode 24 at different times to reduce a level of fibrillation of the fibrillated cartilage joint surface. In various embodiments of the invention, sufficient thermal energy is delivered electrode 22 or 24 to, (i) change the fibrillated cartilage surface to a smooth or smoother surface, (ii) reduce a level of fibrillation of the fibrillated cartilage surface, (iii) cause at least a portion of a plurality of cartilage strands coupled to the fibrillated cartilage surface to create a smoothened cartilage surface, (iv) cause at least a portion of a plurality of cartilage strands coupled to the fibrillated cartilage surface to melt onto the fibrillated cartilage surface or (v) melt at least a portion of a plurality of cartilage strands to create a smoothened cartilage surface.
First electrode 22 has a first thermal energy delivery surface configured to deliver thermal energy to cartilage strands 34 and second electrode 24 has a second thermal energy delivery surface configured to deliver thermal energy to cartilage strands 36. Thermal energy includes but is not limited to RF, microwave, resistive heating, ultrasound, coherent or incoherent light and a thermal jet source. By delivering the appropriate amount of thermal energy to joint surface 28, strands 34 and 36 move out of joint surface 28 and the surfaces of cartilage beds 30 and 32 are smoothened. Additionally, delivered thermal energy can remove some or substantially all of cartilage strands 34 and 36 from joint surface 28. The delivery of thermal energy physically smooths the surface
7 -
RECTIFIED SHEET (RULE 91) ISA/EP of cartilage beds 30 and 32, changes the ultrastructure of the cartilage, stimulates cartilage replication and growth and changes the chemical environment in joint surface 28 and cartilage beds 30 and 32 to relieve pain
Apparatus 10 is used to modify the geometry of cartilage strands 34 and 36 through cartilage shnnkage and possibly limited ablation of strands 34 and 36
Distal end 14 of probe 12 is inserted through an arthroscope to joint surface 28 First and second electrodes 22 and 24 are introduced into joint surface 28 Sufficient thermal energy is delivered from electrodes 22 and 24 to shnnk at least a portion of cartilage strands 34 and 36, causing the strands to e down on cartilage beds 30 and 32 The delivery of thermal energy to joint surface 28 results in an "ironing" of cartilage strands 34 and 36 onto cartilage beds 30 and 32
Sufficient thermal energy is delivered from first and second electrodes 22 and 24 to shrink at least a portion of cartilage strands 34 and 36 without ablating more than 25% of cartilage beds 30 and 32 In one embodiment, sufficient energy is delivered by first and second electrodes 22 and 24 to raise the temperature of joint surface in the range of 45 to 90 degrees C, preferably 45 to 75 degrees C and more preferably 50 to 70 degrees C Maintenance of a suitable temperature, and the delivery of thermal energy to joint surface 28, is sufficient to cause strands 34 and 36 to become at least partially melted onto the cartilage joint surface while minimizing ablation of cartilage beds 30 and 32
Insulator 26 and first and second electrodes 22 and 24 are configured to be inserted into joint surface 28 Probe 12 is moved back and forth through joint surface 28 to deliver a sufficient amount of thermal energy to strands 34 and 36 to cause them to lie down on their respective cartilage beds The thermal energy delivery surfaces of first and second electrodes 22 and 24 can move along the surfaces of cartilage beds 30 and 32 to complete the ironing effect
Referring now to Figure 4, distal end 14 of probe 12 can have a coiled geometry as well as a variety of geometric configurations Preferably, distal end 14 is malleable or sufficiently flexible to impart movement of first and second electrodes 22 and 24 Distal end 14 can pivot, be hinged, be articulated, or made of a shaped memory metal, and the like, in order to enable first and second electrodes 22 and 24 to follow the contours of joint surface 28
As shown in Figure 5, first and second electrodes 22 and 24 can be operated in a bipolar mode This concentrates the flow of RF energy between first and second electrodes 22 and 24 and diverts direct RF energy flow away from cartilage beds 30 and 32 RF energy which is directed between first and second electrodes 22 and 24 heats up fluids within joint surface 28 and provides a more controlled delivery of energy to cartilage strands 34 and 36 RF ablation of cartilage beds 30 and 32 is reduced
First and second electrodes 22 and 24 can have a vanety of different geometric configurations As illustrated in Figure 6. first and second electrodes 22 and 24 are symmetrically shaped with radiused edges Elimination of sharp edges at an electrode surface reduce the creation of hot spots of thermal energy delivered to a site In Figure 7, first and second electrodes 22 and 24 have rectangular geometries with non-radiused edges First and second electrodes 22 and 24 can each have different sizes and geometries First and second electrodes 22 and 24 can be mirror images of each other or they can be different
Referring now to Figure 8, first and second electrodes 22 and 24 are formed on a periphery of insulation surfaces 18 and 20 respectively In this embodiment, each electrode 22 and 24 defines a first and a second nonconducting region 38 and 40 on an insulator surface 18 and 20 within an interior of first and second electrodes 18 and 20 Non-conducting regions 38 and 40 can be the actual surface of insulator 16, or may be additional structures, each with a non-conducting surface, that are formed on insulation surfaces 18 and 20
First and second sensors 42 and 44 can be provided and associated with first and second electrodes 22 and 24 to measure temperature and/or impedance First and second sensors 42 and 44 are positioned on a surface of first and second electrodes 22 and 24. on a surface of probe 12, on non-conducting regions 38 and 40, or can be advanced and retracted from distal end 14 to and from joint surface 28.
First and second sensors 42 and 44 are of conventional design, including but not limited to thermistors, thermocouples, resistive wires, and the like. Suitable thermal sensors 42 and 44 include a T type thermocouple with copper constantene, J type, E type, K type, fiber optics, resistive wires, thermocouple IR detectors, and the like. Sensors 42 and 44 need not be thermal sensors.
Sensors 42 and 44 measure temperature and/or impedance to permit monitoring and a desired level of energy delivered determined This reduces ablation damage to cartilage beds 30 and 32. If at any time sensor 42 or 44 determines that a desired temperature is exceeded, then an appropriate feedback signal is received at thermal energy source 26 which then regulates the amount of energy delivered to first and second electrodes 22 and 24
Sensors 42 and 44 are positioned on non-conducting regions 38 and 40 in Figure 9. Non-conducting regions 38 and 40 have a variety of geometric surfaces including but not limited to planar, non-planar, concave, convex, and the like. In one embodiment, non-conducting regions 38 and 40 are closer to the midline of insulator 16 than first and second electrodes 22 and 24. This enhances the bipolar conduction of thermal energy between electrodes 22 and 24 in the bipolar mode of operation.
First and second electrodes 22 and 24 can have various geometries including but not limited to cylindrical, semi-cylindrical, rectangular, cubic, irregularly shaped, toroidal (Figure 10), non-circular toroidal (Figure 1 1), non- symmetrical, non-symmetrical toroidal (Figure 12) or be segmented and capable of multiplexing (Figures 13 and 14). In one embodiment, first electrode 22 has a toroidal geometry, first sensor 42 is positioned on non-conducting region 38, and distal end 14 is flexible and curved.
Figure 16 illustrates a block diagram of a temperature/impedance feedback system useful with apparatus 10. Thermal energy is delivered to first and second electrodes 22 and 24 by thermal energy source 26, and applied to
- 10 -
RECTIFIED SHEET (RULE 91) ISA/EP cartilage strands 34 and 36 A monitor 56 ascertains tissue impedance, based on the energy delivered to tissue, and compares the measured impedance value to a set vaiue If the measured impedance exceeds the set value a disabling signal 48 is transmitted to thermal energy source 26, ceasing further delivery of thermal 5 energy to first and second electrodes 22 and 24. If measured impedance is within acceptable limits, energy continues to be applied During the application of thermal energy to cartilage strands 34 and 36, sensor 42 measures the temperature at the surface of sensor 42 A comparator 50 receives a signal representative of the measured temperature and compares this value to a pre-set
10 signal representative of the desired temperature Comparator 50 sends a signal to thermal energy source 26 to continue sending thermal energy, to increase or decrease the level of delivered thermal energy, or to cease delivery of thermal energy
An output 52 from temperature comparator 50 can be input to thermal
' 5 energy source 26 to regulate the amount of power delivered Output 54 from impedance monitor 56 can be input to control the temperature at joint surface 28
Referring now to Figure 17, thermal energy source 26 is coupled to first and second electrodes 22 and 24 and apply a biologically safe voltage to
-0 cartilage strands 34 and 36 In the embodiment illustrated in Figure 1 1, apparatus 10 is represented as a bipolar ablation device First and second electrodes 22 and 24 are connected to a primary side of transformer windings 58 and 60 The common primary windings 58 and 60 are magnetically coupled with a transformer core to secondary windings 58' and 60'
5 The primary windings 58 of the first transformer t, couple the output voltage of apparatus 10 to the secondary windings 58' The primary windings 60 of the second transformer t2 couple the output current of ablation apparatus 10 to the secondary windings 60*
Measuring circuits determine the root mean square (RMS) values or
0 magnitudes of the current and voltage. These values, represented as voltages, are inputted to a diving circuit D to geometrically calculate, by dividing the RMS
- 1 1 -
RECTIFIED SHEET (RULE 91) ISA/EP voltage value by the RMS current value, the impedance of the tissue site at sensor 42.
The output voltage of the divider circuit D is presented at the positive (+) input terminal of comparator A. A voltage source V0 supplies a voltage across the variable resistor R.., thus allowing one to manually adjust the voltage presented at the negative input of comparator A. This voltage represents a maximum impedance value beyond which power will not be applied to electrode 22 Specifically, once the tissue is heated to a temperature corresponding to an impedance value greater than the maximum cut-off impedance, thermal energy source 26 stops supplying energy to first and second electrodes 22 and 24.
Comparator A can be of any of a commercially available type that is able to control the amplitude or pulse width modulation of thermal energy source 26 The temperature within joint surface 28 can be controlled based on the tissue impedance, as represented by signal 62, or based on tissue temperature, as represented by signal 64. In one embodiment, the switch S is activated to allow the impedance signal 62 to enter the positive (+) input terminal of comparator A. This signal along with the reference voltage applied to the negative (-) input terminal actuates comparator A to produce an output signal. If the selected tissue ablation site is heated to a biologically damaging temperature, the tissue impedance will exceed a selected impedance value seen at the negative (-) input terminal, thereby generating disabling signal 48 to disable thermal energy source 26, ceasing the energy supplied to first and second electrodes 22 and 24.
The output signal of comparator A may either disable thermal energy source's 26 energy output, depending on the tissue temperature as reflected by its impedance.
The foregoing description of a preferred embodiment of the invention has been presented for purposes of illustration and description. It is not intended to be exhaustive or to limit the invention to the precise forms disclosed. Obviously, many modifications and variations will be apparent to practitioners skilled in this art It is intended that the scope of the invention be defined by the following claims and their equivalents. What is claimed is
- u

Claims

1 A thermal energy delivery apparatus comprising a probe means including a distal end and a proximal end a first electrode means positioned at the distal end of the probe means, wherein the first electrode means is configured to deliver sufficient thermal energy to a fibnllated cartilage surface to reduce a level of fibrillation of the fibnllated cartilage surface, and a cabling means coupled to the proximal end of the probe means
2 The apparatus of claim 1 further comprising means for distancing the first electrode means from the fibnllated cartilage surface
3 The apparatus of claim 1 , further comprising an offset member means positioned at the distal end of the probe means and configured to distance the first electrode means from the fibnllated cartilage surface
4 The apparatus of claim 1 , further comprising a second electrode means positioned on the probe means
5 The apparatus of claim 1, wherein the apparatus is a bipolar device
6 The apparatus of claim 1 , wherein the apparatus is a monopolar device
7 The apparatus of claim 1. wherein the first and second electrode means are configured to minimize damage to a cartilage bed underlying the fibnllated cartilage surface
8 The apparatus of claim 7, further comprising a sensor means positioned at the distal end of the probe means
9 The apparatus of claim 1 , further comprising a thermal energy source means coupled to the cabling means
10 The apparatus of claim 1 , wherein the thermal energy source is selected from RF. microwave, resistive heating, ultrasound, coherent or incoherent light and a liquid thermal jet
1 1 The apparatus of claim 1 , wherein the distal end of the probe means is sized to contract a joint.
12 The apparatus of claim 1, wherein the distal end of the probe means is sized to contract an articulated joint.
13 The apparatus of claim 9, further comprising a sensor means positioned at the distal end of the probe means, a comparator means configured for comparing a measured temperature value at the sensor means with a predetermined temperature value and generating a disabling signal if the measured temperature value exceeds the predetermined maximum temperature value, and a communication means for communicating the disabling signal to the thermal energy source means to cease further delivery of energy from the thermal energy source means to the first electrode means.
14 A thermal energy delivery apparatus, comprising a probe means including a distal end and a proximal end, a first thermal energy delivery surface positioned at one side of the distal end of the probe means, wherein the first thermal energy delivery surface is configured to deliver sufficient thermal energy to a fibrillated cartilage surface to reduce a level of fibrillation of the fibrillated cartilage surface, a thermal energy insulator positioned adjacent to the first thermal energy delivery surface on an opposing second side of the distal end of the probe means. and a cabling means coupled to the proximal end of the probe means
15 A thermal energy delivery apparatus, comprising a probe means including a distal end and a proximal end, a first electrode means positioned at the distal end of the probe means, wherein the first electrode means is configured to deliver sufficient thermal energy to an irregular cartilage surface to reduce a level of irregularity of the fibrillated cartilage surface, and a cabling means coupled to the proximal end of the probe means
16 An apparatus configured to be positioned adjacent to a fibrillated cartilage joint surface, comprising a probe means with a distal end and a proximal end, an insulator means with a first surface and a second surface, a first electrode means positioned on the first surface of the insulator with a first thermal energy delivery surface configured to deliver sufficient thermal energy to a plurality of cartilage strands coupled to the fibrillated cartilage joint surface to reduce a level of fibrillation of the fibrillated cartilage joint surface, a second electrode means positioned on the second surface of the insulator, and a cable means coupled to the proximal end of the probe means
17 The apparatus of claim 16, further comprising a thermal energy source means coupled to the first electrode means
18 The apparatus of claim 17, wherein the thermal energy source is selected from RF, microwave, resistive heating, ultrasound, coherent or incoherent light and a liquid thermal jet
19 The apparatus of claim 17, wherein the thermal energy source means is coupled to the second electrode means
20 The apparatus of claim 16 wherein the distal end of the probe means is sized to contract a joint
21 The apparatus of claim 16, wherein the distal end of the probe means is sized to contract an articulated joint
22 The apparatus of claim 16, wherein the first electrode means is formed on a peπphery of a first surface of the insulator and defines a first non- conducting region between the first electrode means
23 The apparatus of claim 22, wherein the second electrode means is formed on a peπphery of an opposing second surface of the insulator means and defines a second non-conducting region between the second electrode means
24 The apparatus of claim 16, wherein the first electrode means has a toroidal geometry defining a first non-conducting interior region
25 The apparatus of claim 16, wherein the first electrode means has a non-circular toroidal geometry defining a first non-conducting inteπor region
26 The apparatus of claim 16, wherein the first electrode means has a segmented toroidal geometry defining a first non-conducting interior region
27 The apparatus of claim 16. wherein the first electrode means has a segmented non-circular toroidal geometry defining a first non-conducting interior region
28 The apparatus of claim 23, wherein the second electrode means has a toroidal geometry defining a second non-conducting interior region
29 The apparatus of claim 23, wherein the second electrode means has a non-circular toroidal geometry defining a second non-conducting interior region
30 The apparatus of claim 23, wherein the second electrode means has a segmented toroidal geometry defining a second non-conducting interior region
31 The apparatus of claim 23, wherein the second electrode means has a segmented non-circular toroidal geometry defining a second non- conducting interior region
32 The apparatus of claim 22, wherein the first non-conducting interior region has a concave surface
33 The apparatus of claim 23, wherein the second non-conducting intenor region has a concave surface
34 The apparatus of claim 22, wherein a first sensor means is positioned at the first non-conducting interior region
35 The apparatus of claim 23, wherein a second sensor means is positioned at the second non-conducting intenor region
36 The apparatus of claim 16, wherein at ieast a portion of the probe means is malleable
37 The apparatus of claim 16, wherein the first and second electrode means operate in a bipolar mode
38 The apparatus of claim 16, wherein the first and second electrode means operate in a monopolar mode
39 The apparatus of claim 17, further comprising a sensor means positioned at the distal end of the probe means, a comparator means for comparing a measured temperature value at the sensor means with a predetermined temperature value and generating a disabling signal if the measured temperature value exceeds the predetermined maximum temperature value, and a communication means for communicating the disabling signal to the thermal energy source means to cease further delivery of energy from the thermal energy source means to the first electrode means.
40 A method for modifying a geometry of a fibrillated cartilage surface, comprising providing a thermal energy delivery device including a probe means with a distal end and a thermal energy delivery surface, providing a thermal energy source coupled to the thermal energy deliver. surface, positioning the thermal energy delivery surface adjacent to the fibrillated cartilage surface, and delivering sufficient thermal energy from the thermal energy delivery to reduce a level of fibrillation of the fibrillated cartilage surface
41 The method of claim 40, wherein sufficient thermal energy is delivered from the thermal energy delivery surface to modify the fibrillated cartilage surface to a smooth surface
42 The method of claim 40, wherein sufficient thermal energy is delivered from the thermal energy delivery surface to create a less fibrillated, fibrillated cartilage surface
43 The method of claim 40, wherein sufficient thermal energy is delivered from the thermal energy delivery surface to cause at least a portion of a plurality of cartilage strands coupled to the fibrillated cartilage surface to create a smoothened cartilage surface
44 The method of claim 40, wherein sufficient thermal energy is delivered from the thermal energy delivery surface to cause at least a portion of a plurality of cartilage strands coupled to the fibrillated cartilage surface to melt onto the fibrillated cartilage surface
45 The method of claim 37, wherein a melting of at least a portion of a plurality of cartilage strands creates a smoothened cartilage surface
46 The method of claim 40, wherein the thermal energy delivery surface remains distanced from the fibrillated cartilage surface
47 The method of claim 40, further comprising measuring a temperature of an area adjacent to the fibrillated cartilage surface with a sensor, comparing a measured temperature at the area adjacent to the fibrillated cartilage surface to a predetermined temperature value and generate a signal representative of a difference between the measured temperature and the predetermined temperature value, and transmitting to the thermal energy source a signal to cease further thermal energy delivery if the measured temperature exceeds the predetermined temperature
48 The method of claim 40. wherein the thermal energy source is an RF source
49 The method of claim 40, wherein the thermal energy source is a microwave source
50 The method of claim 40, wherein the thermal energy source is a resistive heating source
51 The method of claim 40, wherein the thermal energy source is an ultrasonic source
52 The method of claim 40, wherein the thermal energy source is a coherent or incoherent light source
53 The method of claim 40, wherein the thermal energy source is a liquid thermal jet source
54 A method for treating chondromalacia on a joint surface, comprising providing a thermal energy delivery device including a probe means with a distal end and a thermal energy delivery surface, providing a thermal energy source coupled to the thermal energy delivery surface, positioning the thermal energy delivery surface adjacent and distanced from a fibrillated cartilage joint surface, and delivering sufficient thermal energy from the thermal energy delivery device to reduce a level of fibrillation of the fibrillated cartilage joint surface
55 The method of claim 54, wherein sufficient thermal energy is delivered from the thermal energy delivery surface to modify the fibrillated cartilage joint surface to a smooth surface
56 The method of claim 54, wherein sufficient thermal energy is delivered from the thermal energy delivery surface to create a less fibrillated, fibrillated cartilage joint surface
57 The method of claim 54, wherein sufficient thermal energy is delivered from the thermal energy delivery surface to cause at least a portion of a plurality of cartilage strands coupled to the fibrillated cartilage joint surface to create a smoothened cartilage joint surface.
58. The method of claim 54, wherein sufficient thermal energy is delivered from the thermal energy delivery surface to cause at least a portion of a plurality of cartilage strands coupled to the fibrillated cartilage joint surface to melt onto the fibrillated cartilage joint surface
. it . 59 The method of claim 58, wherein a melting of at least a portion of a plurality of cartilage strands creates a smoothened cartilage joint surface
60 The method of claim 54, wherein the thermal energy delivery surface remains distanced from the fibrillated cartilage joint surface
61 The method of claim 54, further comprising measuring a temperature of an area adjacent to the fibrillated cartilage joint surface with a sensor, comparing a measured temperature at the area adjacent to the fibrillated cartilage joint surface to a predetermined temperature value and generate a signal representative of a difference between the measured temperature and the predetermined temperature value, and transmitting to the thermal energy source a signal to cease further thermal energy delivery if the measured temperature exceeds the predetermined temperature
62 A method for treating chondromalacia on a joint surface, comprising providing a thermal energy delivery device including a probe means with a distal end and a thermal energy delivery surface, providing a thermal energy source coupled to the thermal energy delivery surface, positioning the thermal energy delivery surface on a fibrillated cartilage joint surface; and delivering sufficient thermal energy from the thermal energy delivery device to reduce a level of fibrillation of the fibrillated cartilage joint surface
63 A method for treating chondromalacia on a joint surface, comprising providing a thermal energy delivery device including a probe means with a distal end and a thermal energy delivery surface, providing a thermal energy source coupled to the thermal energy delivery surface, positioning the thermal energy delivery surface adjacent and distanced from an irregular cartilage joint surface, and delivering sufficient thermal energy from the thermal energy delivery device to reduce a level of irregularity of the irregular cartilage joint surface
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