AU2001224345A1 - Apparatus for and treatment of the intervertebral disc - Google Patents
Apparatus for and treatment of the intervertebral discInfo
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- probe
- disc
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Description
APPARATUS FOR AND TREATMENT OF THE INTERVERTEBRAL DISC
1. Field of the Invention
The present invention relates generally to advances in medical systems and procedures for prolonging and improving human life. More particularly, this invention relates to a method and apparatus for thermally treating the intervertebral disc to relieve pain associated with abnormalities of the disc due to pathology of the disc or interruption of the various neural processes in and around the disc.
2. Description of the Related Art
The use of radiofrequency electrodes for ablation of tissue in the body or for the treatment of pain is known. In a typical application, a radiofrequency probe or a resistive heating probe may be constructed in an elongated, cylindrical configuration and inserted into the body to a target tissue which is to be treated or ablated. In the case of a radiofrequency probe, there may be an exposed conductive tip portion and an insulated poπion of the probe. When connected to an external source of radiofrequency power, heating of tissue occurs near the exposed conductive portion of the probe, whereby therapeutic changes in the target tissue near the conductive tip are created by the elevation of temperature of the tissue. Thermal probes can also be made by resistive heating of a portion of the probe so as to heat surrounding tissue by thermal conduction. By reference, the products of Radionics, Inc., located in Burlington, Massachusetts, include commercially available radiofrequency generators and electrode systems of varied configurations. A paper by Cosman, et al, entitled "Theoretical Aspects of Radiofrequency Lesions in the Dorsal Root Entry Zone", Neurosurgery, December 1984, Vol. 15, No. 6, pp. 945-950, describes aspects of tissue heating using radiofrequency electrodes and probes.
The use of thermal therapy in and around the spinal column is also known. Heating of an intervertebral disc to relieve pain is described in commonly assigned U.S. Patent No. 5,433,739 entitled "Method and Apparatus for Heating an Intervertebral Disc for Relief of Back Pain" and in commonly assigned U.S. Patent No. 5,571,147 entitled "Thermal Dennervation of an Intervertebral Disc for Relief of Back Pain", the contents of each patent being incorporated herein by reference. In these patents, electrodes are described for either radiofrequency or resistive thermal heating of all or a portion of the intervertebral disc. Straight, curved, and flexible-tipped electrodes are described for this purpose.
U.S. Patent No. 6,007,570 to Sharkey/Oratec Interventions discloses an intervertebral disc apparatus for treatment of the disc. The apparatus includes a catheter having a self-navigating intradiscal section in the form of a conventional helical coil. In use, the intradiscal section is advanced through the nucleus pulpous and is manipulated to navigate within the nucleus along the inner wall of the annulus fibrosis. An energy delivering member incorporated into the apparatus adjacent the intradiscal section supplies energy to treat the disc area.
The apparatus disclosed in Sharkey '570 is subject to several disadvantages which detract from its usefulness in relieving pain associated with an interveπebrai disc. For example, navigation of the helical coil of the catheter within the nucleus pulpous requires the support structure to wrap around in an approximately circular fashion from the anterior portion to the posterior portion of the intervertebral disc. This circumticious path of the support structure is difficult for the surgeon to effectuate. Moreover, the configuration of the helical support structure increases the risk of probe kinking and is deficient in consistently facilitating the prescribed movement within the disc.
It is desirable to treat the posterior or posterior/lateral portion of the intervertebral disc for the indication of mechanical degeneration of the disc and discogenic back pain. Pain can be derived from degeneration or compression of the inter,- ertebral disc in its posterior or posterior/lateral portions. There is some
denervation of the intervertebral disc near the surface of the disc and also within its outer portion known as the annulus fibrosis. Fissures or cracks within the disc caused by age, mechanical trauma, or disc denervation are believed to be associated with painful symptoms.
Accordingly, the present invention is directed to a novel apparatus and method of use which provides for direct and confirmable placement of a thermal or electromagnetic field (EMF) treating element within the posterior/lateral and posterior portions of an intervertebral disc for thermal treatment. The apparatus includes a percutaneously introducable thermal device having a novel configuration which provides excellent torque transmission and an increased flexure in a specific direction thereby facilitating the advancement of the thermal device near the surface of a degenerative disc and preferably within the outer annulus.
SUMMARY
The present invention is a novel and improved system and method for approaching the interveπebrai disc through a percutaneous insertion from the back of a patient. In one embodiment, the surgical apparatus includes an elongated thermal or electromagnetic field creating probe member having a guidable region adjacent its distal end with an undulating groove defined in its outer surface. The undulating groove is dimensioned to facilitate bending of the guidable region in at least one radial direction preferably, opposed radial directions, of movement relative to a longitudinal axis of the thermal probe. Preferably, the guidable region includes a plurality of undulating grooves, whereby adjacent undulating grooves are longitudinally spaced with respect to each other. The undulating grooves each define a sinusoidal configuration which may be arranged about an undulating axis extending in oblique relation to the longitudinal axis . The guidable region includes a longitudinally extending backbone which facilitates the desired bending of the guidable region.
The apparatus may also include a cannula to facilitate introduction of the thermal probe into the intervertebral disc. The cannula defines a iumεn to receive the
thermal probe with the thermal probe being advanceable within the lumen. The cannula includes an arcuate end portion dimensioned to arrange the guidable region of the thermal probe at a desired orientation within the annulus fibrosis. The cannula may define a penetrating distal end dimensioned to penetrate the intervertebral disc. Impedance measuring means are associated with the cannula to monitor the impedance of tissue adjacent a distal end of the cannula to provide an indication relating to tissue condition or type.
A method for relieving pain associated with an intervertebral disc having a disc nucleus pulpous and an outer annulus fibrosis surrounding the nucleus pulpous is also disclosed. The method includes the steps of introducing a thermal or electromagnetic field (EMF) transmitting element of a probe into the annulus fibrosis of the intervertebral disc and supplying thermal or EMF energy from an appropriate source to the transmitting element to heat the annulus fibrosis adjacent the transmitting element sufficiently to relieve pain associated with the intervertebral disc.
BRIEF DESCRIPTION OF THE DRAWINGS
The features of the apparatus and method of the present invention will become more readily apparent and may be better understood by referring to the following detailed descriptions of illustrative embodiments of the present disclosure, taken in conjunction with the accompanying drawings, wherein:
FIG. 1 illustrates the apparatus in accordance with the present invention inseπed percutaneously into the annulus fibrosis of an intervertebral disc;
FIG. 1A is a view illustrating an alternate use of the apparatus of FIG. 1;
FIG. 2 is a schematic view of the apparatus in a disassembled condition illustrating the inseπion cannula, thermal or EMF probe and associated auxiliary electronic components;
FIG. 3 is a perspective view of the thermal probe of the apparatus:
FIGS. 4A and 4B are enlarged views of the guidable region of the thermal or EMF probe illustrating the undulating cuts to facilitate bending movement of the guidable region in a predetermined direction;
FIG. 5 is a cross-sectional view of the guidable region taken along the lines 5-5 of FIG. 3;
FIG. 6 is a side cross-sectional view of the guidable region;
FIG. 7 is a cross-sectional view similar to the view of FIG. 5 and illustrating an alternate embodiment of the thermal or EMF probe;
FIG. 8 is a perspective view of a guidable region of another alternate embodiment of the thermal or EMF probe; and
FIG. 9 is a side view of the guidable region of another alternate embodiment of a thermal or EMF probe according to the present disclosure.
DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS
The apparatus of the present disclosure provides a more precise controlled positioning of a thermal probe in an interveπebrai disc targeted for treatment. It will be readily apparent to a person skilled in the an that the apparams and method of use of the apparatus can be used to treat/destroy body tissues in any body cavity or tissue locations that are accessible by percutaneous or endoscopic catheters or open surgical techniques, and is not limited to the disc area. Application of the device and method in all of these organs and tissues are intended to be included within the scope of this invention.
In the drawings and the following description, the term "proximal", as is traditional, will refer to the end of the apparatus, or component thereof, which is closest to the operator, and the term "distal" will refer to the end of the apparams, or component thereof, which is more remote from the operator.
Referring now to Figure 1, the apparams of the present disclosure is shown positioned within an intervεπebral disc. Prior to a detailed discussion of the apparatus, a brief overview of the anatomy of the interveπεbral disc is presented. The
intervertebral disc "D" is comprised of an outer annulus fibrosis "A" and an inner nucleus pulpous "N" disposed within the annulus fibrosis "A". The annulus fibrosis "A" consists of a tough fibrosis material which is arranged to define a plurality of annular cartilaginous rings "R" forming the natural striata of the annulus. The nucleus pulpous "N" consists primarily of an amorphous gel having a softer consistency than the annulus "A". The nucleus pulpous "N" usually contains 70% - 90% water by weight and mechanically functions similar to an incompressible hydrostatic material. The juncture or transition area of the annulus fibrosis "A" and nucleus pulpous "N" generally defines, for discussion purposes, an inner wall "W" of the annulus fibrosis "A". The disc cortex "C" surrounds the annulus fibrosis "A". The posterior, anterior and lateral aspects of the intervertebral disc are identified as "P", "AN" and "L", respectively, with the opposed posterior-lateral aspects identified as "PL" .
When mechanical stress is put upon a disc or when a disc degenerates with age, fissures, illustrated by the cracks "F" in the drawings, may occur in the posterior or posterior/lateral poπions of thε disc "D". Problems with the nerves and fissures "F" and degenerative discs can give rise to various patient problems, such as back or leg pain originating from the irritation or occurrence of these abnormalities. Applicants have realized that heating and/or electromagnetic field (EMF) therapy of the interveπebrai disc, preferably, the annulus "A" in the posterior "P" or posterior-lateral "PL" poπions, will result in alterations and thermal ablation of thesε structurεs which will in mm producε alleviation of pain and healing of the disc. Thus, it is desirable, as shown in Figure 1 , to have a practical method of placing a thermal or electromagnetic probe in the posterior "P" and/or posterior-lateral "PL" poπion of a disc "D" where these neural and aberrant structures occur for the reliεf of pain and othεr disc related problems.
Thε apparams of thε prεsεnt invention will now be described. Refeπing now to FIGS. 1 and 2, apparams 100 includes outer insertion cannula 102, thermal or EMF probe 104 which is positionable within ώe cannula 102 and power source 106 which is connected to thε thermal probe 102. Cannula 102 preferably includes a rigid
tubular shaft 108 defining a longitudinal axis "a" and having a rigid curved or arcuate portion 110 adjacent its distal end, angularly offset with respect to the longitudinal axis "a". Shaft 108 is preferably composed of a conductive material such as stainless steel or other suitable composition and is insulated with insulation along most of its length as indicated by the hatching in FIGS. 1 and 2. Alternatively, shaft 108 may be fabricated from a suitable polymeric material and formed by conventional injection molding techniques. The distal end portion 112 of shaft 108 may be left uninsulated or exposed to permit electrical connection (e.g., for impedance measuring, etc.) to or contact with the tissue as cannula 102 is placed in the tissue. Alternatively, exposed portion 112 may be connected to power source 106 to heat stimulate or micro-thermal generate to facilitate passage through the tissue. The extreme distal tip 114 of shaft 108 is preferably sharpened to facilitate penetration into the disc tissue, i.e., through the bone of thε cortex "C" and into the annulus "A". A handle or housing 116 is connected to the proximal end of cannula shaft 108 to facilitate manipulation of cannula 102. Handle 116 may include an index marker 118 to indicate the direction of arcuate poπion 110 of cannula 102 such that when thermal or EMF probe 104 is introduced within cannula 102, the surgeon may determine in which azimuthal rotational direction the curve is oriented. By reference, electrode shafts and insulation materials are illustrated by the electrodes manufactured by Radionics, Inc., Burlington, Massachusetts.
Cannula shaft 108 may have a diameter ranging from a fraction of a millimeter to several millimetεrs and a length of a few centimeters up to 20 centimeters or more. Alternatively, cannula shaft 108 may be fabricated from an MRI compatible material, including cobalt alloys, titanium, copper, nitinol, etc. Arcuatε portion 110 of cannula 102 may assume a variεty of angular orientations depending on the surgical procedure to be performed. In the preferred embodiment for thermal or EMF therapy of the interveπebrai disc, arcuate poπion 110 is arranged such that thermal or EMF probe 104 is generally deliverεd from cannula 102 in oπhogonal relation to longimdinal axis "a".
Power source or generator 106 may be a radiofrequency generator providing frequency between several kilohertz to several hundred megahertz. An example of a suitable generator is the lesion generator, Model RFG-3C, available from Radionics, Inc., Burlington, Massachusetts. Power source 106 may have a power output ranging from several watts to sevεral hundred watts, depending on clinical need. Power source 106 may have control devices to increase or modulate power output as well as readout and display devices to monitor enεrgy parameters such as voltage, current, power, frequency, temperature impedance 109, etc. , as appreciated by one skilled in the art. Other types of power sources are also contemplated, e.g., including resistive heating units, laser sources, or microwave generators.
Referring now to FIGS. 3-6 in conjunction with FIGS. 1 and 2, thermal or EMF probe 104 of apparams 100 will be discussed. Thermal or EMF probe 104 is positionable within cannula 102 and is adapted for reciprocal longimdinal movement there within. Thermal or EMF probe 104 includes handle 120 and elongated member 122 extending distally from the handle 120. Handle 120 is advantageously dimensionεd for gripping εngagemεnt by thε user and may bε fabricatεd from a suitable polymeric material or compatible metal. Elongated member 104 defines a longimdinal axis "e" and has an exterior wall 124 defining axial bore or lumen 126 (FIG. 5) extεnding substantially along its lεngth within thε εxterior wall. The exterior wall 124 at the proximal end of elongated membεr 122 is solid or continuous. Thε distal end of the elongatεd mεmber includes guidable region 128.
As best depicted in the enlarged plans views of a poπion of guidable region 128 of FIGS. 4A and 4B and the cross-sectional view of FIG. 6, guidable region 128 includes a plurality of interruptεd undulating grooves 130 defined in extεrior wall 124 and spaced along the longitudinal axis "e" of the probe 104. Grooves 130 prefεrably define a generally sinusoidal configuration having a waveform arranged to osculate about an axis "o" (FIG. 4B) extεnding in obliquε relation to the axis "e" of the probe 104. Grooves 130 extend about the circumference of guidable region 128 and preferably extend radially inwardly to communicate with internal lumen i2ό of probε
104 (FIG. 6), aldiough, it is envisioned that grooves 130 may terminate within the exterior wall 124 of probe 104 without communicating with the internal lumen 126.
Grooves 130 extend through a radial arc of approximately 270° - 350° with respect to the longitudinal axis "e". Grooves 130 are interrupted by backbone 132 which extends the length of guidable region 128. In a preferred method of manufacture, each groove 130 is cut within the exterior wall 124 a predεtεrminεd distance to leave a solid portion between the ends of the cuts thereby forming the single backbone 132. Backbone 132 is dimensioned to resist radial arcing movement of guidable region 124 in the direction "A" (FIG. 5) away from the backbone 132 while permitting guidable region 128 to move, via interaction of sinusoidal grooves 130, in radial directions across from the backbone 132 indicated by arrows B and C and as shown in FIG. 5. Such feature provides significant advantages during positioning of guidable region 128 within thε intervertebral disc, including ease of control and guidance into predetermined locations within the disc annulus "a". More specifically, thε undulating groove arrangement permits guidable region 128 to bend or flex in opposed radial directions B and C along one radial plane to follow the ring-like configuration of the natural striata of the annulus fibrosis "A", or alternatively, about the inner wall '"W" separating the annulus "A" and the nucleus "N" while also providing excεllεnt torquε transmission. The undulating groove arrangement also provides a more streamline profile which, consequently, facilitates passage of the probe through the annulus tissue, as compared to conventional helical coil arrangements which are subject to ''catching'' tissue during passage.
The distal tip 134 of guidable region 128 is preferably blunt or rounded to prevεnt undεsired entry or penεtration of thermal probe into areas, including underlying nerves, the nucleus, etc., as will be discussed. The proximal end of thermal or EMF probe 10-!- includes a plurality of etchings or markings 136. Markings 136 indicate thε degree of extension of guidable region 128 from cannula 102.
When used as a radio freαuεncy probε. thermal or EMF probe 104 may be insuiatεd except for guidable region 128 which may be left uninsulated for
transmission of energy. Alternately, thermal or EMF probe 104 may be uninsulated while cannula 102 functions as the insulating element of the apparatus. In this arrangemεnt, the degree of extension of guidable region 128 beyond cannula 102 determines the heating capability of the probe 104.
With continued reference to FIGS. 3 and 5, thermal or EMF probe 104 may further include a thermal sensor 138, e.g., a thermocouple, thermistor, etc. , extending through-its internal lumen 128 and terminating adjacent its distal closed tip (see also FIG. 1). Thermal sensor 138 provides temperature monitoring of the tissue being treated adjacent thermal or EMF probe 104 through temperature monitor 109. Thermal sensor 138 may be connected by extεrnal wires extending through handle and further through an electrical connεction to thε εxtεrnal apparams, such as power source or tempεramrε monitor 109.
Referring particularly to FIGS. 3, 5 and 6, thermal or EMF probe 104 may optionally include a guide wire 140 to facilitate placemεnt of thε thermal or EMF probε 104 into intεrveπebral disc. Guide wire 140 is positionablε within internal lumεn 128 of thermal or EMF probe 104 during insenion of the probe 104 relative to the disc. Guide wire 140 has sufficient rigidity to assist in advancing thermal or EMF probe 104 with annulus "A" while also permitting guidable region 128 of the probe 104 to flex and bend to conform to the path defined by the natural striata or inner annulus wall "W". Guide wire 140 may bε any conventional guide wire suitable for this purpose. Alternatively, guide wire 140 may be a "steerable" guidewire whereby movement of the distal end is controlled through control wires manipulated from the proximal end of the guide wire. Steerable guidewires are known in the an.
As depicted in the cross-sectional view of FIG. 5, thermal or EMF probe 104 may further include an external flexible sleεve 142 which encloses thermal sensor 138 and guide wire 140. Sleeve 142 serves to maintain the alignment of thermal sensor 138 and guide wire 140 within thermal or EMF probe 104 and also prevents or niii-imizes entry of body fluids within the probe 104. Sleeve 142 preferably comprises a flexible polymer aterial, such as polyamide.
With reference again to FIGS. 1 and 2, the remaining components of the apparatus will be discussed. Apparatus 100 preferably includes an imaging system 144 to potentially monitor, control or verify the positioning of cannula 102 and/or thermal probe 104. Imaging systems contemplated, include X-ray machines, fluoroscopic machine or an ultrasonic, CT, MRI, PET, or other imaging device. Several of thesε dεvices have conjugate elemεnts as illustrated by element 146 on the opposite poπion of the patient's body to provide imaging data. For example, if image is an X-ray machine, element may be a detection device, such as an X-ray film, digital, X-ray detector, fluoroscopic device, etc. Use of imaging machines to monitor percutaneously placed electrodes into tissue is commonly practiced in the surgical field.
With continued reference to FIG. 2, in conjunction with FIG. 1, apparams 100 may further include stylet 148 which is to be used in conjunction with cannula 102. Stylet 148 is positionablε within the lumen of cannula 102 and preferably occludes the front opening of the cannula 102 to prevent entry of tissue, fluids, etc., during introduction of the cannula 102 within the intervertebral disc "D". Stylet 148 may include a proximally positioned hub 150 which mates with handle 116 of cannula 102 to lock the components togethεr during insεπion. Such locking mεchanisms are appreciated by one skilled in the art. An impedance monitor 152 can bε connεctεd, as shown by connεction 154, to stylεt 148 and thεrεforε communicate elεctrically with the exposed portion 112 of cannula 102 into which the stylet 148 is introduced to monitor impedance of the tissue adjacent the distal end of cannula 102. Alternatively, connection of the impedance monitor may be made directly to the shaft of cannula 102 whereby impedancε mεasurεments are effεcruated through the exposed distal end of the cannula 102. Once the combination of stylet 148 and cannula 102 are inseπεd into the body, impedance monitoring may determine the position of cannula tip 112 with respect to the patient's skin, the coπex "C" of the disc, the annulus "A", and/or nucleus "NU" of the disc "ID". These regions will have different impedance levels that are readily quantifiable. For examplε, for a fully insulatεd electrode or cannula with an exposed area of a few square millimeters cannula end, the impedance will change signincantiy
from the position of the tip near to or contacting the cortex "C" of the disc to the region where the tip is within the annulus "A" of Figure 1 and further where the tip of the disc is within the nucleus "NU" of the disc. Differences of impedance can range from a few hundred ohms outside the disc, to 200 to 300 ohms in the annulus, to approximately 100 to 200 ohms in the nucleus. This variation can be detεctεd exquisitely by the surgeon by visualizing impedance on meters or by hearing an audio tone whose frequency is proportional to impedance. Such a tone can be generated by monitor 109 in Figure 2. In this way, an independent means is provided for detecting placement of the curved cannula within the disc. Thus, e.g., undesired pεnetration of the tip portion 112 of cannula 102 through the inner wall "W" of the annulus "A" and into the nucleus pulpous "N" can be detectεd via the impedance means.
Stylet 148 can be made of a rigid metal tubing with either a permanent bend 156 at its distal end to correspond to the curvature of arcuate poπion 112 of cannula 102 or may be a straight guide wire to adapt to the curve of the cannula 102 when it is inserted within the cannula 102. The hub 150 and connector 154 can take various forms including luer hubs, plug-in-jack-type connections, integral cables, etc. By reference, example of elεctrodes and cables arε illustrated in the product lines of Radionics, Inc., Burlington, Massachusetts.
Surgical Procedure
The use of the apparatus 100 in accordance with a prefeπεd procεdurε for thermal treatment of an interveπebrai disc will now be discussed. With refεrεncε to FIG. 1, thε targεtεd intervertebral disc "D" is identified during a pre-op phase of the surgery. Access to the. intεrvεπebral disc area is then ascertained, preferably, through percutanεous tεchniquεs or, lεss desirably, open surgical techniques. Cannula 102 with stylet 148 positioned and secured therεin is introduced within thε interveπebrai disc "D" preferably from a posterior or posterior-latεral location as depicted in FIG. 1. Altemaiivεly, cannula 102 may bε utilizεd without stylet 148. During introduction of thε assεmbled components, the impedance of the tissue adjacent thε distal εnd 114 of thε
cannula 102 is monitored through the cannula 102 or alternativεly via the impedance means associated with stylet 148. Impedance monitoring may determine the position of cannula tip 114 with respect to the patient's skin, the cortex "C" of the disc, the annulus "A" and/or the nucleus "N" of the disc. As discussed above, these regions have differεnt and quantifiablε impεdance levels thereby providing an indication to the user of the position of the cannula tip 112 in the tissue. Monitoring of the location of cannula 102 may also be confirmed with imaging system 144. In the preferred procedure, cannula tip 114 of cannula 102 is positioned within the annulus fibrosis "A"of the interveπebrai disc "D" at a posterior lateral "PL" location of the disc "D" without penetrating through annulus wall "W" and into nucleus "N". As appreciated, sharpened tip 114 facilitates entry into the annulus "A".
Therεaftεr, cannula 102 is angulated to position arcuate end poπion 110 of the cannula 102 at the desired orientation within the annulus fibrosis "A". Confirmation of the angular orientation of arcuatε εnd portion 110 of cannula 102 is madε through location of indεx markεr 118 of thε cannula 102. In one prefεrrεd oriεntation, arcuate end poπion 110 is arranged to deliver thermal probe 106 within the posterior section "P" of the intervεπεbral disc "D". In an alternate procedure, arcuate end poπion 110 is arranged to deliver thermal or EMF probe 104 toward the posterior- lateral "PL" and lateral "L" poπion of the disc "D" as shown in phantom in FIG. 1.
Stylet 148 is men removed from cannula 102. Thermal or EMF probe 104 with guide wire 140 assemblεd therein is positioned within the internal lumen of cannula 102 and advanced through the cannula 102 to at least paπially εxposε guidablε region 128 of the thermal or EMF probe 104 from the distal end of cannula 102. As thermal or EMF probe 10-1 entεrs the annulus fibrosis "A", guidablε rεgion 128, due to its strategic configuration and undulating groove 130 aπangement, flexes and conforms to the namrai striata of the annular rings "R" of the annulus fibrosis, i.e., follows a path dεfinεd by the namrai striata. Once positioned, guidable region 128 occupies a substantial portion of thε posterior ~P~ section of thε annulus fibrosis "A" and preferably extends to the opposed posterior lateral section "PL" of the annulus fibrosis.
The degree of extension of guidable region 128 beyond cannula 102 may be indicated by distance or index markings 136 on the shaft of thermal or EMF probe 104 and confirmed through imaging system 144. In the alternate method shown in phantom in FIG. 1, arcuate end portion 110 is angulated to directly access the posterior lateral "PL" section of the annulus fibrosis "A". Thermal or EMF probe 104 is thereafter advanced to position guidable region 128 within the lateral "L" and posterior/lateral "PL" sections of the annulus "A". Similar to the predεscribεd mεthod of application, guidable region 128 follows the arcuate path of the natural striata of the annulus "A" upon advancement therein. In either method, confirmation of the orientation of arcuate end portion 110 is provided through index pin or marker adjacent handle of thε cannula and can be also monitored through imaging system 144.
In an alternate method of application depicted in FIG. 1A, cannula 102 may be positioned adjacent inner wall "W" of annulus. Thermal or EMF probe 104 is advanced within thε annulus fibrosis "A" whεrεby guidablε rεgion 128 follows along thε arcuatε path of innεr wall "W" of the annulus "A" without penetrating through the wall "W" and into the nucleus "N".
Once the guidable region 128 is positioned within thε annulus "A" as desired, the power source 106 is activated wherεby the thermal or EMF probe 104 delivers thermal energy and/or creates an electromagnεtic field through guidable region 128 adjacent the intervεπεbral disc "D" to producε thε thεrmal and/or EMF therapy in accordance with the present invention. Appropriate amounts of power, current or thermal heat may be monitored from the external power source 106 and deliverεd for a certain amount of time as determined appropriate for clinical needs. As appreciated, the degree of extension of guidable region 128 from cannula controls thε volume of disc tissue heatεd by thε probε 104. Thεrmal sensor 138 of thermal or EMF probe 104 can provide information concerning the tεmperamre of tissue adjacent the distal end. The impedance means associated with cannula 102 can provide impedance measurements of the tissue thereby providing an indication of the degree of dessication, powεr rise, or charring, that may be taking place near thε thermal probe tip 134. This indicates the
effectiveness of the treatment and guards against unsafe contraindications of the therapy. By reference, use of impedance monitoring in neurosurgεry is described in the paper by E.R. Cosman and B.I. Cos an, entitled "Methods of Making Nervous System Lesions", in Neurosurgery, Vol. 3, pp. 2490-2499, McGraw Hill 1985.
Thus, the apparatus of the present invention provides significant advantages over the prior aπ.
Cannula 102 and thermal or EMF probe 104 permits the probe to be directed from a location across the posterior margin and into the lateral portion of the disc "D" by a direct pathway along, e.g., the natural striata of the annulus fibrosis or along the inner wall "W" of the annulus fibrosis. This represεnts a morε dirεct approach to the posterior/lateral portions of the disc than thε more circuital approach invoking delivering a probe into the nucleus center of the disc and then arcing the probe around through an anterior or anterior-lateral pathway through the nucleus "N" . Moreovεr, thε prεsent invεntion εliminates the neεd to pεnetrate the annulus wall "W" and enter the nucleus "N" with a guide.
A further advantage of the present invention is that by monitoring impedance of cannula 102 and/or thermal or EMF probe 104 as it is being positioned within the disc, the surgeon can get additional information on the positioning of the cannula 102 as it is being put into the proper orientation.
A furthεr advantagε of thε prεsent invention is that by use of a curved introduction cannula a more εfficacious dirεction of the probe can be achievεd in thε difficult lumbar or lumbar-sacral intεrveπebral discs. In these approaches, nearby heavy bony structures, such as the iliac crest, can often obscure a placement of a curved probe parallεl to thε end plates or bony margins of adjacent intervεπebral discs. By appropriate angulation and rotation of a curved cannula, the extension of a thεrmal probe parallel to the so-called end plates of the interveπεbral discs is made possible with minimal repositioning and manipulation of the introduction cannula.
The undulating groove arrangement and backbone of the guidable region of the thermal probe permits flexing in at least opposed radial directions along one
radial plane to follow the arcuate path in the intervertebral disc. The undulating groove arrangement also provides a. streamline profile thereby facilitating entry and passage through the annulus tissue.
In typical radiofrequency procedures using the apparatus and process of the present invention, power levels of fractions of a watt to several tens of watts may be used depending on the extent of heating requirεd and the degrεe of therapy, denervation, and disc healing that is desired to be achieved.
A further advantage of the present system and method is that it enables simple, minimally-invasive, percutaneous, out-patient treatment of intradiscal pain without the need for open surgery as for example discectomiεs or spinal stabilization using plates, screws, and other instrumentation hardware. A further advantage of the present invention is that it is simple to usε and relatively economical. Compared to open surgery, the treatmεnt of disc by pεrcutaneous electrodε placεmεnt represents only a few hours procedure and minimal hospitalization, with minimal morbidity to the patient. Open surgical procedures often requirε full anεsthεtic, extensive operating room time, and long hospital and home convalescence. Such open surgeriεs havε considerable risk of morbidity and mortality and are much more expensive than a percutaneous procedure as dεscribεd in accordance with the presεnt invention.
It is also envisioned that thermal or EMF probe could be, or incorporate, a resistive heating elεmεnt(s) to hεat thε annulus fibrosis by rεsistivε heating. For example, within the distal end there may be a resistive wire such as a nichrome wire or other type of resistive element, such that current delivered to the resistive elεmεnt from thε powεr gεnεrator will produce resistive heating within the elemεnt. Such hεating of the proximate disc material when the electrode is inseπεd into the disc of a patient. Various construction details for such resistive heating εlements can be devised by those skilled in the aπ. For example, a resistivε wire can bε fabricated to produce the guidablε rεgion. Alternatively, an internal resistive wire can be placed inside thε guidable region. The overall shaft may be coated with an insulative matεrial or other material to produce appropriate frictionai, thermal, or elεc ricai characteristics of the
electrode when it is placed in the disc. Like the high frequency electrode embodimεnt, as described above, such a resistive elemεnt may have the appropriate flexibility, or steering capability so that it can be steered or directed favorably within the appropriate portion of the posterior and posterior-lateral portions of a disc, as illustrated by the discussion associated with Figure 1 above.
In another configuration of the thermal probe, in accordance with the presεnt disclosure, the distal end may comprise a microwave antenna system or a laser fiber with transducer to distribute energy through thermal element into surrounding disc tissue. In the configuration shown in Figure 1, the thermal transmitting element operatεs as a microwave antenna or laser transmitting element, respectively. Other constructions to produce a heating element can be devised by those skilled in the art and are intendεd to be included widiin the scope of the present invention. It is further envisionεd that the thermal or EMF probe can be positioned such that the transmitting guidable region is disposεd within thε nucleus "N".
Refεrring now to thε cross-sεctional viεw of FIG. 7, an alternate embodimεnt of thε probε of thε present invention is disclosed. This probe is substantially similar to the probe of thε prior embodiment but, includes, a second backbone 132 in diametrical opposed relation to the first backbone 132. Second backbone 132 is created by interrupting the sinusoidal grooves 130 adjacent the area of the second backbone 132. This double backbone arrangement permits radial movement along one plane in directions B and C, but, also enhances rigidity of the guidable region, which may be desirable in certain surgical applications.
Refεrring now to FIG. 8, thεre is illustrated an alternate embodimεnt of thε probε of thε presεnt invention. This probe is similar to the probε 104 of thε first embodiment, but, includes a single continuous sinusoidal groove 170 extending the length of the guidable region 172. This configuration provides for uniform radial movement in all radial directions with respεct to thε longimdinal axis. Such configuration may bε advantageous when inserting probe along a more sεrpenticious
path. Groove 170 extends to communicate with the internal lumen of the probe as discussed hereinabove.
Referring now to FIG. 9, there is illustrated another alternate embodiment of thermal or EMF probe 104. Thermal or EMF probe 104 includes a guidable region 200 having a plurality of partial annular grooves 202 or cuts spaced along the longitudinal axis "Z". FIG. 9 is an enlarged plan view of a poπion of guidable region 200. In the prefεrrεd embodiment, annular grooves 202 radially extend about the exterior wall through an arc which is slightly less than 360°, thereby providing a solid region 204, 206 between the respective starting and ending positions of the groove. Adjacent grooves 202 are radially displaced at about 180°. The overall effect of this arrangement is that guidable region can flex uniformly in all radial directions. This configuration is advantageous in insertion of the probε along a morε sεrpentinus path.
While the above description contains many specifics, these specifics should not be construed as limitations on the scope of the disclosure, but merely as exemplifications of prefεπεd εmbodiments thereof. Those skilled in the aπ will envision many other possible variations that are within the scope and spirit of the disclosure as defined by the claims appendεd hereto.
Claims (10)
1. A surgical apparatus for thermal or electromagnetic treatment of tissue, which comprises: an elongated thermal probe member having proximal and distal ends and defining a longitudinal axis, the probe member having a guidable region adjacent the distal end, the guidable region having an undulating groove defined in an outer surface thereof and being dimensioned to facilitate bending of the guidable region in at least one radial direction of movement relative to the longitudinal axis, the thermal probe being adapted for connection to a thermal energy source to provide thermal energy to tissue.
2. The surgical apparatus according to claim 1 wherein the guidable region includes a plurality of undulating grooves, adjacent undulating grooves longitudinally spaced with respect to each other.
3. The surgical apparatus according to claim 2 wherein the undulating grooves each define a sinusoidal configuration.
4. The surgical apparatus according to claim 3 wherein the guidable region includes a longitudinally extending backbone, the backbone being devoid of the undulating grooves and being dimensioned to resist bending of the guidable region in a radial direction movement.
5. The surgical apparatus according to claim 1 wherein the one undulating groove is arranged about an undulating axis extending in oblique relation to the longitudinal axis.
6. The surgical apparatus according to claim 2 wherein the probe member defines an internal lumen, the undulating grooves extending to communicate with the internal lumen.
7. The surgical apparatus according to claim 2 including a cannula to facilitate introduction of the thermal probe into the intervertebral disc, the cannula defining a lumen to receive the thermal probe, the thermal probe being advanceable within the lumen.
8. The apparatus according to claim 4 wherein the cannula includes an arcuate end portion, the arcuate end portion dimensioned to arrange the guidable region of the thermal prove to a desired orientation within the annulus fibrosis.
9. The apparatus according to claim 5 wherein the cannula defines a penetrating distal end dimensioned to penetrate the intervertebral disc.
10. The apparatus according to claim 5 wherein the cannula includes an index marker adjacent a proximal end thereof to indicate a direction of the arcuate end portion.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| AU2006200294A AU2006200294B2 (en) | 2000-09-07 | 2006-01-23 | Apparatus for and treatment of the intervertebral disc |
Applications Claiming Priority (3)
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|---|---|---|---|
| US23075000P | 2000-09-07 | 2000-09-07 | |
| US60/230,750 | 2000-09-07 | ||
| PCT/US2000/034140 WO2002019933A1 (en) | 2000-09-07 | 2000-12-18 | Apparatus for and treatment of the intervertebral disc |
Related Child Applications (1)
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|---|---|---|---|
| AU2006200294A Division AU2006200294B2 (en) | 2000-09-07 | 2006-01-23 | Apparatus for and treatment of the intervertebral disc |
Publications (2)
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| AU2001224345A1 true AU2001224345A1 (en) | 2002-06-13 |
| AU2001224345B2 AU2001224345B2 (en) | 2005-11-17 |
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| AU2001224345A Ceased AU2001224345B2 (en) | 2000-09-07 | 2000-12-18 | Apparatus for and treatment of the intervertebral disc |
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| AU2434501A Pending AU2434501A (en) | 2000-09-07 | 2000-12-18 | Apparatus for and treatment of the intervertebral disc |
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| US (4) | US6604003B2 (en) |
| EP (2) | EP1582166B1 (en) |
| JP (1) | JP4219679B2 (en) |
| AU (2) | AU2434501A (en) |
| CA (1) | CA2419991C (en) |
| DE (2) | DE60020171T2 (en) |
| ES (2) | ES2240225T3 (en) |
| WO (1) | WO2002019933A1 (en) |
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- 2000-12-18 AU AU2001224345A patent/AU2001224345B2/en not_active Ceased
- 2000-12-18 WO PCT/US2000/034140 patent/WO2002019933A1/en active IP Right Grant
- 2000-12-18 DE DE60035378T patent/DE60035378T2/en not_active Expired - Lifetime
-
2001
- 2001-09-06 US US09/948,409 patent/US6604003B2/en not_active Expired - Fee Related
-
2003
- 2003-05-16 US US10/439,881 patent/US6980862B2/en not_active Expired - Fee Related
-
2005
- 2005-11-03 US US11/266,569 patent/US7702397B2/en not_active Expired - Fee Related
-
2010
- 2010-04-05 US US12/754,046 patent/US20100274243A1/en not_active Abandoned
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