WO1997006738A1 - Ablation apparatus and system for removal of soft palate tissue - Google Patents

Ablation apparatus and system for removal of soft palate tissue Download PDF

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Publication number
WO1997006738A1
WO1997006738A1 PCT/US1996/013189 US9613189W WO9706738A1 WO 1997006738 A1 WO1997006738 A1 WO 1997006738A1 US 9613189 W US9613189 W US 9613189W WO 9706738 A1 WO9706738 A1 WO 9706738A1
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WO
WIPO (PCT)
Prior art keywords
distal end
cannula
electrode
uvula
ofthe
Prior art date
Application number
PCT/US1996/013189
Other languages
French (fr)
Inventor
Stuart D. Edwards
Edward J. Gough
David Douglass
Original Assignee
Somnus Medical Technologies, 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 Somnus Medical Technologies, Inc. filed Critical Somnus Medical Technologies, Inc.
Priority to AU70078/96A priority Critical patent/AU7007896A/en
Publication of WO1997006738A1 publication Critical patent/WO1997006738A1/en

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    • A61B18/20—Surgical instruments, devices or methods for transferring non-mechanical forms of energy to or from the body by applying electromagnetic radiation, e.g. microwaves using laser
    • A61B18/22—Surgical instruments, devices or methods for transferring non-mechanical forms of energy to or from the body by applying electromagnetic radiation, e.g. microwaves using laser the beam being directed along or through a flexible conduit, e.g. an optical fibre; Couplings or hand-pieces therefor
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Definitions

  • This invention relates generally to an ablation apparatus for the removal of a variety of tissues, and more particularly to an RF, microwave, or laser fiber apparatus which ablates soft palate tissue including a portion ofthe uvula to treat snoring disorders.
  • snoring there are two types of snoring. They are distinguished, depending on the localization of their origin.
  • the first type of snoring, velar is produced by the vibration of all ofthe structures ofthe soft palate including the velum, the interior and posterior arches ofthe tonsils and the uvula.
  • Velar snoring results from a vibration ofthe soft palate created by the inspiratory flow of air, both nasal and oral, which makes the soft palate wave like a flag. The sound intensity of these vibrations is accentuated by the opening ofthe buccal cavity which acts as a sound box.
  • the second type, pharyngeal snoring is a kind of rattle, including even horn whistling.
  • portions ofthe soft palate have been removed by laser ablation. If too much tissue is removed, severe consequences result.
  • the degree of laser ablation is difficult to control and multiple treatments are usually required. Further, patients have a high degree of soreness in their throats for many weeks.
  • U.S. Patent No. 4,423,812 discloses a loop electrode design characterized by a bare active wire portion suspended between wire supports on an electrode shaft. Tissue striping is effected with a bare wire, and the adjacent portions ofthe wire supports an electrode shaft that is made insulating to prevent accidental burns to the patient, allowing the physician to use these insulated parts to help position and guide the active wire portion during the surgical procedure. However, this requires that the physician shave off, during multiple visits, successive thin superficial layers ofthe obstructing tissues to avoid gross resection and its adverse affects.
  • U.S. Patent No. 5,046,512 discloses a method for the treatment of snoring and apnea.
  • the method regulates air flow to the user to an extent comparable to the volume of air which flows through the users nasal passages.
  • An associated apparatus provides a device having a body portion sufficiently wide to separate the users teeth. It includes an air passage comparable in area to the area ofthe user's nasal passages.
  • oral cavity appliances has been proposed frequently for the treatment of sleep disorders. It has been recognized that movement ofthe mandible forward relative to the maxilla can eliminate or reduce sleep apnea and snoring symptoms by causing the pharyngeal air passage to remain open.
  • Several intra-oral dental appliances have been developed which the user wears at night to fix the mandible in an anterior protruded position.
  • Such dental appliances essentially consist of acrylic or elastomeric bit blocks, similar to orthodontic retainers or athletic mouth guards, which are custom fitted to a user's upper and lower teeth. The device may be adjusted to vary the degree of anterior protrusion.
  • U.S. Patent 4,901,737 discloses an intra-oral appliance while reducing snoring which repositions the mandible in an inferior, open, and anterior, protrusive, position as compared to the normally closed position of the jaw.
  • an appropriate mold is taken for the maxillary dentition and ofthe mandibular dentition to form an appliance template.
  • This device includes a pair of V-shaped spacer members formed from dental acrylic which extend between the maxillary and mandibular dentition to form a unitary mouthpiece.
  • an ablation apparatus which eliminates the need for dental appliances for the treatment of snoring and sleep apnea disorders. It would also be desirable to provide a treatment device which is not an intra-oral dental appliance, and which can effectively and safely remove selected portions ofthe soft palate without providing the patient with undesirable side effects. Further, it would be desirable to provide a tissue ablation device which retains the targeted ablation tissue during the ablation process. SUMMARY OF THE INVENTION Accordingly, it is an object ofthe invention to provide an ablation device which is useful with a variety of tissues, and includes a retaining member to retain the tissue as it is ablated. Another object ofthe present invention is to provide an ablation apparatus to treat snoring disorders.
  • Yet another object ofthe invention is to provide an ablation apparatus to ablate sections ofthe uvula and other soft palette tissue.
  • Still another object ofthe invention is to provide an ablation apparatus including an anvil to position the uvula for ablation.
  • Another object ofthe invention is to provide an ablation apparatus including an anvil to position and retain the uvula and other soft palate tissue during ablation.
  • a further object ofthe invention is to provide an ablation apparatus which uses an RF energy source to ablate selected sections ofthe uvula and other soft palate tissue.
  • Another object ofthe invention is to provide an ablation apparatus which includes an anvil to position and retain the uvula and other soft palate tissue during ablation, with the anvil being capable of being retracted to a distal end of a cannula coupled to the anvil.
  • the retainer member has a distal end that extends in a lateral direction relative to an anvil longitudinal axis.
  • the distal end is adapted to retain a selected tissue during the ablation process.
  • One or more energy delivery devices are slideably positioned in the cannula.
  • An advancement and retraction apparatus advances and retracts the energy delivery devices in and out ofthe cannula distal end and into the tissue retained at the retainer member distal end.
  • a soft palate ablation system has a handle with a distal end and a proximal end.
  • a cannula is provided with a distal end, a proximal end coupled to the handle distal end, and a lumen.
  • a soft palate retaining member is coupled to the cannula distal end and extends beyond the cannula distal end.
  • the soft palate retaining member includes a distal end that extends in a lateral direction relative to a soft palate retaining member longitudinal axis to retain a selected soft palate tissue to be ablated.
  • An energy delivery device has a distal end that is capable of extending beyond the distal end ofthe cannula.
  • An energy source is coupled through a cable to the energy delivery device.
  • a variety of different tissues can be ablated, included but not limited to soft, hard, and mucosal tissue, as well as cartilage.
  • the present invention is particularly suitable in ablating soft palate tissue for purposes of ablation and effecting a cure for snoring.
  • the uvula can be retained by the retaining member as one or more energy delivery devices are advanced and retracted out ofthe uvula. Once the desired level of uvula ablation is achieved, the retaining member can be rotated and retracted in order to provide a straight shot for the energy delivery devices to be introduced into tissue that does not require retainment during ablation,
  • a variety of retaining members can be utilized including but not limited to an anvil, net, hooks, graspers, and the like. Further, different energy sources can be employed such as RF, microwave, laser, and the like.
  • the energy delivery device can be an RF electrode (operated in mono-polar and bi-polar modes), a microwave antenna, an optical delivery fiber and the like.
  • the retaining member particularly the anvil, extends past the distal end ofthe cannula and includes a laterally deflected distal end which serves to capture and retain the soft palate tissue, particularly the uvula. It may be desirable to remove the retaining member in order to permit the energy delivery devices to extend beyond the former position ofthe retaining member distal end.
  • an insulator can be positioned to surround the RF electrode and may be capable of slideable movement along an exterior ofthe electrode. This permits the length of an RF ablation surface to be varied. Further, the distal end ofthe anvil can be a ground pad electrode.
  • One or more sensors can be incorporated at the cannula distal end and in the retaining member and its distal end.
  • the retaining member can have a hollow central lumen with one or more fluid distribution ports.
  • a visualization apparatus can be positioned in the lumen.
  • An eyepiece is coupled to the visualization apparatus at a proximal end ofthe cannula.
  • a flushing port can be formed in the cannula lumen.
  • the flushing port is positioned near a distal end ofthe visualization apparatus in order to introduce a flushing medium past visualization apparatus distal end.
  • FIGURES Figure 1(a) is a perspective view ofthe tissue ablation apparatus ofthe present invention, including a retaining member that is in the form of an anvil.
  • Figure 1(b) is a perspective view ofthe retaining member which is in the form of a basket or net.
  • Figure 1(c) is a perspective view ofthe retaining member which is in the form of a pair of graspers.
  • Figure 1(d) is a perspective view ofthe tissue ablation apparatus ofthe present invention, including a rotatable retaining member coupled to a vacuum source.
  • Figure 2 is a perspective view ofthe cannula with a needle electrode or antenna and a retaining member that is in the form of an anvil.
  • Figure 3 is a perspective view ofthe distal end ofthe cannula and an energy delivery device extending beyond the cannula's distal end, establishing an optical length.
  • Figure 4 is a perspective view of a distal end ofthe cannula, with a thermal sensor and an anvil.
  • Figure 5 is a perspective view ofthe apparatus ofthe present invention with a handle.
  • Figure 6 is an exploded view ofthe retaining member and the cannula.
  • Figure 7 is a perspective view of a flushing port or optic port associated with the retaining member.
  • Figure 8 is a block diagram illustrating the inclusion of a controller, power source and other electronic components ofthe present invention.
  • Figure 9 is a block diagram illustrating an analog amplifier, analog multiplexer and microprocessor used with the present invention.
  • a soft tissue ablation apparatus 10 includes a cannula 12, a cannula distal end 12', a cannula proximal end 12" and a cannula lumen 12'".
  • a retaining member 14 is coupled to cannula 12 and extends beyond distal end 12'.
  • Retaining member 14 has a distal end 14' that extends in a lateral direction relative to a longitudinal axis of retaining member 14.
  • Distal end 14' is adapted to capture, receive and retain a tissue ablation target during the ablation process.
  • tissue can be ablated, included but not limited to soft, hard, and mucosal tissue, as well as cartilage.
  • the present invention is particularly suitable in ablating soft palate tissue for purposes of ablation and effecting a cure for snoring.
  • the uvula can be retained by retaining member 14 as one or more energy delivery devices are advanced and retracted out ofthe uvula. Once the desired level of uvula ablation is achieved, retaining member 14 can be rotated, retracted in order to provide a straight shot for energy delivery devices to be introduced into tissue that does not require retainment during ablation.
  • Retaining member 14 can be fastened with a fastener 16, including but not limited to a ground adjustment nut, and to the body of cannula 12.
  • retaining member 14 can be integrally formed with cannula 12.
  • a retaining member proximal end 14" can include a flushing port 14"' that is adapted to receive a flushing medium.
  • Retaining member 14 can have a variety of different geometries such as an anvil (Figure 1(a)), a net or basket (Figure 1(b)), a grasper ( Figure 1(c)), and the like. Retaining member 14 physically retains and constrains the movement of a targeted ablation tissue before, during and after ablation
  • Shrink insulation may be provided around the section of retaining member 14 that is adjacent to fastener 16.
  • One or more energy delivery devices 18 are positioned in lumen 12'". Energy delivery devices 16 can be advanced out of distal end 12* and introduced into the selected tissue target. Alternatively, energy delivery devices 16 can remain stationary in lumen 12'". Cannula 12 is advanced and retracted in order to introduce and retract energy delivery devices 18 in and out ofthe soft palate tissue. Energy delivery devices 18 can be of many varieties, including but not limited to an RF electrode 18 coupled to an RF energy source, a laser optical fiber 18 coupled to a laser source, a microwave antenna 18, and the like. Energy delivery devices 18 can have a sharpened distal end in order to pierce the targeted ablation tissue. A suitable RF electrode 18 is a needle electrode.
  • a deployment and retraction device 20 can be used to advance and retract energy delivery source 18 in and out of distal end 12' and the targeted ablation tissue.
  • Deployment and retraction device 20 includes one or more actuators 20' that are mechanically coupled to energy delivery devices 18.
  • Actuators 20' can be a variety of different knobs and the like that are hand activated.
  • Actuators 20' can be positioned on an exterior surface of a handle 22 and moved axially, along gradation marks 20" to advance or retract.
  • Gradation marks 20" provide an indication of, (i) the extension length of energy delivery devices 18 or (ii) the length of energy delivery devices 18 that is an ablation surface. Other movements of actuators 20' are suitable as long as they provide the appropriate advancement and retraction of energy delivery devices 18.
  • retainer member provides for the retention ofthe uvula upon the application of a vacuum, Figure 1(d).
  • a vacuum source 21 extends to retainer member 14.
  • the soft palate tissue including but not limited to the uvula, is positioned within an interior of retainer member 14. Vacuum is applied and the soft palate tissue is retained. With the soft palate tissue retained, electromagnetic energy delivery device is introduced into the soft palate tissue. Alternatively, upon application of vacuum, the electromagnetic energy delivery device can include a geometry that at least partially surrounds an exterior ofthe soft palate tissue. Electromagnetic energy is then applied to an exterior ofthe soft palate.
  • a handle 22 includes a distal end 22' and a proximal end 22".
  • Cannula 12 can be at least partially positioned in handle 22, or at least coupled to distal end
  • cannula 12 also extends past proximal end 22".
  • a multi- plug 24 extends from proximal end 22", out of an adapter 26 coupled to proximal end 22" or out of proximal end 12".
  • Multi-plug 24 receives a variety of different cables or lines that are coupled to sensors 36, energy delivery devices 18 and other devices. For example, multi-plug 24 can receive lines coupled to,
  • a light source cable 30 can be coupled to handle 22, adaptor 26 or distal end 12'.
  • Energy delivery device 18 can remain in a fixed position relative to cannula 12. In this instance, cannula 12 itself is advanced and retracted from distal end 22' in order to introduce and retract energy delivery devices 18 in and out ofthe targeted ablation tissue.
  • An eyepiece can be coupled at a proximal end of soft tissue ablation apparatus, e.g., to proximal end 22", proximal end 12' or adaptor 26.
  • FIG. 2 more fully illustrates distal end 12'.
  • a visualization apparatus 32 is positioned in lumen 12'" and can be positioned adjacent to energy delivery device 18. As shown, visualization apparatus extends to distal end 12'. It will be appreciated that visualization apparatus can be slideably positioned in lumen 12'" and advance beyond distal end 12'. Further, visualization apparatus 32 can be retained in lumen 12'" and cannula 12 can itself be advanced causing visualization apparatus 32 to move.
  • Visualization apparatus 32 includes optics, an illumination source such as a plurality of optical fibers, and the like, as is well known to those skilled in the art.
  • an optical path length is established. It is within this optical path length that visualization is established.
  • energy delivery device 18 is introduced into the uvula.
  • a suitable topical anesthetic includes but is not limited to lidocaine and can be administered out of an aperture formed in retaining member 14, cannula 12, and the like. The ablation ofthe targeted tissue is under full visualization. Distal end 14' holds the uvula in place as the lidocaine is sprayed and energy delivery device 18 introduced.
  • insulation layer 34 is positioned around the exterior of energy delivery device 18 when it is an RF electrode.
  • a slideable insulation layer 34 surrounds electrode 12.
  • insulation 34 can comprise a polyimide material, a thermal sensor 36 positioned on top ofthe polyimide insulation, and a .002 inch shrink wrap.
  • the polyimide insulating layer is semi-rigid. Sensor 36 can lay down substantially the entire length ofthe polyimide.
  • Figure 5 illustrates the mechanical attachment of deployment apparatus 20 with energy delivery device (RF electrode 18'). Further, handle 22 is more readily adapted to be held as a trigger. An actuator 20"' is positioned at the exterior of handle 22 and is advancement back and forth along gradation marks 20" to adjust the length of insulation layer 34 that covers RF electrode 18'. This provides a variable area of RF electrode 18' that serves as the RF energy ablation surface.
  • retaining member 14 can be removed completely away from cannula 12. This permits soft tissue ablation apparatus 10 to be used in a variety of soft tissue applications besides the uvula, including but not limited to other soft palate structures, the turbinates and the like. Alternatively, retaining member 14 is slightly rotated and withdrawn past distal end 12'.
  • a flushing aperture 38 is included in retaining member 14 to spray a flushing medium across visualization apparatus 32, particularly the optics, in order to clean visualization apparatus 32. This provides a clean view ofthe site. Additionally, a flushing aperture can be included in distal end 12'.
  • One or more thermal sensors 36 can be positioned at distal end 14', at distal end 12', at a distal end of energy delivery device 18, as well as other positions to measure temperature and determine when sufficient energy has been applied to the soft tissue.
  • Sensors 36 provide temperature measurement and monitoring ofthe target to be ablated and permit a desired level of ablation to be achieved without necrosing too much tissue. This reduces damage to surrounding tissue. By monitoring the temperature at a central point within the interior ofthe selected mass, a determination can be made when ablation is complete. If at any time sensor 36 determines that a desired ablation temperature is exceeded, then an appropriate feedback signal is received at the energy source which then regulates the amount of power delivered to energy delivery device 18. By monitoring temperature, power delivery can be accelerated to a predetermined or desired level. In the case of RF energy, impedance is used to monitor voltage and current. The readings of sensors 36 regulate voltage and current that is delivered to the tissue site.
  • the output for these sensors 36 is used by a controller, described further in this disclosure, to control the delivery of energy to the tissue site.
  • Resources which can be hardware and/or software, are connected with the thermal sensors 36, the power source and to energy delivery device 18.
  • the resources provide an output for delivering and maintaining a selected energy delivery device 18. Further the resources provide an output that maintains a selected RF energy for a selected length of time. If RF energy is used, the resources are associated with sensors 36, a ground pad electrode (if included) as well as the RF power source for maintaining a selected power at RF electrode 18 independent of changes in voltage or current. Sensors
  • thermocouple 36 are of conventional design, including but not limited to thermistors, thermocouple, resistive wires, and the like.
  • Suitable thermal sensors 36 include a T type thermocouple with copper constantene, J type, E type, K type, thermistors, fiber optics, resistive wires, thermocouple IR detectors, and the like. It will be appreciated that sensors 36 need not be thermal sensors.
  • a control signal is generated by controller 50 that is proportional to the difference between an actual measured value, and a desired value.
  • the control signal is used by power circuits 52 to adjust the power output in an appropriate amount in order to maintain the desired power delivered at the respective RF electrode 18.
  • temperatures detected at the thermal sensors 36 provide feedback for maintaining a selected power.
  • the actual temperatures are measured at temperature measurement device 54, and the temperatures are displayed at user interface and display 48.
  • a control signal is generated by controller 50 that is proportional to the difference between an actual measured temperature, and a desired temperature.
  • the control signal is used by power circuits 52 to adjust the power output in an appropriate amount in order to maintain the desired temperature delivered at the respective sensor.
  • Controller 50 can be a digital or analog controller, or a computer with software.
  • controller 50 When controller 50 is a computer it can include a CPU coupled through a system bus. On this system can be a keyboard, a disk drive, or other non-volatile memory systems, a display, and other peripherals, as are known in the art. Also coupled to the bus are a program memory and a data memory.
  • User interface and display 48 includes operator controls and a display.
  • Controller 50 can be coupled to imaging systems, including but not limited to ultrasound, CT scanners and the like.
  • Diagnostics can be performed optically, with ultrasound, CT scanning, and the like. Diagnostics are performed either before, during and after treatment.
  • controller 50 uses the output of current sensor 42 and voltage sensor 44 to maintain the selected power level at RF electrode 18.
  • the amount of RF energy delivered controls the amount of power.
  • a profile of power delivered can be incorporated in controller 50, and a pre-set amount of energy to be delivered can also be profiled.
  • Circuitry, software and feedback to controller 50 result in process control, and the maintenance ofthe selected power that is independent of changes in voltage or current, and are used to change, (i) the selected power, including RF, microwave, laser and the like, (ii) the duty cycle (on-off and wattage), (iii) bipolar energy delivery and (iv) fluid delivery, including flow rate and pressure.
  • process variables are controlled and varied, while maintaining the desired delivery of power independent of changes in voltage or current, based on temperatures monitored at the thermal sensors 36.
  • Analog amplifier 56 can be a conventional differential amplifier circuit for use with the thermal sensors 36.
  • the output of analog amplifier 56 is sequentially connected by an analog multipexer 58 to the input of A/D converter 60.
  • the output of analog amplifier 56 is a voltage which represents the respective sensed temperatures.
  • Digitized amplifier output voltages are supplied by A/D converter 60 to a microprocessor 62.
  • Microprocessor 62 may be a model no. 68HCII available from Motorola. However, it will be appreciated that any suitable microprocessor or general purpose digital or analog computer can be used to calculate impedance or temperature.
  • Microprocessor 62 sequentially receives and stores digital representations of impedance and temperature. Each digital value received by microprocessor 62 corresponds to different temperatures and impedances.
  • Calculated power and impedance values can be indicated on user interface and display 48.
  • calculated impedance and power values can be compared by microprocessor 62 with power and impedance limits. When the values exceed predetermined power or impedance values, a warning can be given on user interface and display 48, and additionally, the delivery of RF energy can be reduced, modified or interrupted.
  • a control signal from microprocessor 62 can modify the power level supplied by power source 64.
  • An imaging system can be used to first define the volume ofthe targeted ablation tissue that will be ablated.
  • Suitable imaging systems include but are not limited to, ultrasound, CT scanning, X-ray film, X-ray fluoroscope, magnetic resonance imaging, electromagnetic imaging and the like. The use of such devices to define a volume of a tissue mass or a tumor is well know to those skilled in the art.
  • an ultrasound transducer transmits ultrasound energy into a region of interest in a patient's body.
  • the ultrasound energy is reflected by different organs and different tissue types. Reflected energy is sensed by the transducer, and the resulting electrical signal is processed to provide an image ofthe region of interest. In this way, the volume to be ablated is ascertained.

Abstract

An ablation apparatus includes a probe with a distal end, a proximal end and a lumen. An anvil is coupled to the probe and extends beyond the probe distal end. The anvil has a distal end that extends in a lateral direction relative to an anvil longitudinal axis. The distal end is adapted to receive and position an uvula or other soft tissue. One or more energy delivery devices are slideably positioned in the probe. The energy delivery devices are advanced and retracted in and out of the probe distal end. An advancement and retraction apparatus advances and retracts the energy delivery devices in and out of the probe distal end and into the soft tissue retained at the anvil distal end. The soft tissue ablation apparatus can further include a handle with a lumen, a proximal end and a distal end. The probe is at least partially positioned in the handle lumen and extends beyond the handle distal end. The ablation apparatus is useful for ablation of soft palate tissue to eliminate snoring.

Description

ABLATION APPARATUS AND SYSTEM FOR REMOVAL OF SOFT PALATE TISSUE
Cross Reference to Related Applicationς This application is a continuation-in-part application of U.S. Serial No.
08/239,658, filed May 9, 1994, having named inventors Stuart D. Edwards et al. (Attorney Docket No. VCAR 1012), and is incoφorated herein by reference.
BACKGROUND OF THE INVENTION Field of he Invention
This invention relates generally to an ablation apparatus for the removal of a variety of tissues, and more particularly to an RF, microwave, or laser fiber apparatus which ablates soft palate tissue including a portion ofthe uvula to treat snoring disorders.
Description of Related Art
Generally, there are two types of snoring. They are distinguished, depending on the localization of their origin. The first type of snoring, velar, is produced by the vibration of all ofthe structures ofthe soft palate including the velum, the interior and posterior arches ofthe tonsils and the uvula. Velar snoring results from a vibration ofthe soft palate created by the inspiratory flow of air, both nasal and oral, which makes the soft palate wave like a flag. The sound intensity of these vibrations is accentuated by the opening ofthe buccal cavity which acts as a sound box. The second type, pharyngeal snoring, is a kind of rattle, including even horn whistling. It is caused by the partial obstruction ofthe oropharyngeal isthmus by the base ofthe tongue with, now and again, its total exclusion by the tongue base becoming jammed against the posterior wall ofthe pharynx. This results in a sensation of breathing, apnea, which constitutes the sleep apnea syndrome.
These two types of snoring may easily be combined in the same individual. For some years there have been surgical techniques for correcting apnea. However, maxillary surgery to cure pharyngeal snoring requires major surgery, with the operation lasting several hours, and the uvula-palatopharnygoplasty procedure to correct velar snoring is not without draw backs. This explains the popularity of prosthesis and other preventive devices.
More recently, portions ofthe soft palate have been removed by laser ablation. If too much tissue is removed, severe consequences result. The degree of laser ablation is difficult to control and multiple treatments are usually required. Further, patients have a high degree of soreness in their throats for many weeks.
U.S. Patent No. 4,423,812 discloses a loop electrode design characterized by a bare active wire portion suspended between wire supports on an electrode shaft. Tissue striping is effected with a bare wire, and the adjacent portions ofthe wire supports an electrode shaft that is made insulating to prevent accidental burns to the patient, allowing the physician to use these insulated parts to help position and guide the active wire portion during the surgical procedure. However, this requires that the physician shave off, during multiple visits, successive thin superficial layers ofthe obstructing tissues to avoid gross resection and its adverse affects. U.S. Patent No. 5,046,512 discloses a method for the treatment of snoring and apnea. The method regulates air flow to the user to an extent comparable to the volume of air which flows through the users nasal passages. An associated apparatus provides a device having a body portion sufficiently wide to separate the users teeth. It includes an air passage comparable in area to the area ofthe user's nasal passages.
The use of oral cavity appliances has been proposed frequently for the treatment of sleep disorders. It has been recognized that movement ofthe mandible forward relative to the maxilla can eliminate or reduce sleep apnea and snoring symptoms by causing the pharyngeal air passage to remain open. Several intra-oral dental appliances have been developed which the user wears at night to fix the mandible in an anterior protruded position. Such dental appliances essentially consist of acrylic or elastomeric bit blocks, similar to orthodontic retainers or athletic mouth guards, which are custom fitted to a user's upper and lower teeth. The device may be adjusted to vary the degree of anterior protrusion.
U.S. Patent 4,901,737 discloses an intra-oral appliance while reducing snoring which repositions the mandible in an inferior, open, and anterior, protrusive, position as compared to the normally closed position of the jaw. Once the dentist or physician determines the operative snoring reduction position for a particular patient, an appropriate mold is taken for the maxillary dentition and ofthe mandibular dentition to form an appliance template. This device includes a pair of V-shaped spacer members formed from dental acrylic which extend between the maxillary and mandibular dentition to form a unitary mouthpiece.
While such dental appliances have proven effective in maintaining the mandible in a protruded position to improve airway patency, they often result in undesirable side effects. One ofthe most common side effects is aggravation of the tempromandibular joint and related jaw muscles and ligaments, especially in individuals who have a tendency to grind their teeth during sleep. Aggravation ofthe tempromandibular joint has be associated with a wide variety of physical ailments, including migraine headaches. Accordingly, many individuals suffering from sleep apnea and snoring disorders are not able to tolerate existing anti- snoring dental appliances for long periods of time.
It would be desirable to provide an ablation apparatus which eliminates the need for dental appliances for the treatment of snoring and sleep apnea disorders. It would also be desirable to provide a treatment device which is not an intra-oral dental appliance, and which can effectively and safely remove selected portions ofthe soft palate without providing the patient with undesirable side effects. Further, it would be desirable to provide a tissue ablation device which retains the targeted ablation tissue during the ablation process. SUMMARY OF THE INVENTION Accordingly, it is an object ofthe invention to provide an ablation device which is useful with a variety of tissues, and includes a retaining member to retain the tissue as it is ablated. Another object ofthe present invention is to provide an ablation apparatus to treat snoring disorders.
A further object ofthe invention is to provide an ablation apparatus which can use a variety of energy sources to remove soft palate tissue and treat snoring disorders. Yet a further object ofthe invention is to provide an ablation apparatus which can use a variety of energy sources, includes a retaining member to retain the tissue as it is ablated, and is suitable for ablating soft, hard, cartilage and mucosal tissues.
Yet another object ofthe invention is to provide an ablation apparatus to ablate sections ofthe uvula and other soft palette tissue.
Still another object ofthe invention is to provide an ablation apparatus including an anvil to position the uvula for ablation.
Another object ofthe invention is to provide an ablation apparatus including an anvil to position and retain the uvula and other soft palate tissue during ablation.
A further object ofthe invention is to provide an ablation apparatus which uses an RF energy source to ablate selected sections ofthe uvula and other soft palate tissue.
Another object ofthe invention is to provide an ablation apparatus which includes an anvil to position and retain the uvula and other soft palate tissue during ablation, with the anvil being capable of being retracted to a distal end of a cannula coupled to the anvil.
Yet another object ofthe invention is to provide an ablation system that includes a retaining member to retain an ablated tissue site, and the retaining member can be retracted so that an energy delivery source can be utilized without the retaining member. Still a further object ofthe invention is to provide an ablation system with a retaining member to retain an ablated tissue site, as well as resources providing an output for delivering and maintaining a selected energy at the energy delivery device in order to achieve a desired level of ablation. These and other objects ofthe present invention are achieved in an ablation apparatus that includes a cannula with a distal end, a proximal end and a lumen. A retainer member is coupled to the cannula and extends beyond the cannula distal end. The retainer member has a distal end that extends in a lateral direction relative to an anvil longitudinal axis. The distal end is adapted to retain a selected tissue during the ablation process. One or more energy delivery devices are slideably positioned in the cannula. An advancement and retraction apparatus advances and retracts the energy delivery devices in and out ofthe cannula distal end and into the tissue retained at the retainer member distal end. In another embodiment ofthe invention, a soft palate ablation system has a handle with a distal end and a proximal end. A cannula is provided with a distal end, a proximal end coupled to the handle distal end, and a lumen. A soft palate retaining member is coupled to the cannula distal end and extends beyond the cannula distal end. The soft palate retaining member includes a distal end that extends in a lateral direction relative to a soft palate retaining member longitudinal axis to retain a selected soft palate tissue to be ablated. An energy delivery device has a distal end that is capable of extending beyond the distal end ofthe cannula. An energy source is coupled through a cable to the energy delivery device.
A variety of different tissues can be ablated, included but not limited to soft, hard, and mucosal tissue, as well as cartilage. The present invention is particularly suitable in ablating soft palate tissue for purposes of ablation and effecting a cure for snoring. The uvula can be retained by the retaining member as one or more energy delivery devices are advanced and retracted out ofthe uvula. Once the desired level of uvula ablation is achieved, the retaining member can be rotated and retracted in order to provide a straight shot for the energy delivery devices to be introduced into tissue that does not require retainment during ablation, A variety of retaining members can be utilized including but not limited to an anvil, net, hooks, graspers, and the like. Further, different energy sources can be employed such as RF, microwave, laser, and the like. The energy delivery device can be an RF electrode (operated in mono-polar and bi-polar modes), a microwave antenna, an optical delivery fiber and the like.
The retaining member, particularly the anvil, extends past the distal end ofthe cannula and includes a laterally deflected distal end which serves to capture and retain the soft palate tissue, particularly the uvula. It may be desirable to remove the retaining member in order to permit the energy delivery devices to extend beyond the former position ofthe retaining member distal end.
This is achieved by either removing the retaining member from the cannula, or alternatively, rotating and retracting the retaining member distal end. In this manner, the apparatus ofthe present invention can be used to introduce energy delivery devices beyond the distal end ofthe retaining member. When an RF electrode is used, an insulator can be positioned to surround the RF electrode and may be capable of slideable movement along an exterior ofthe electrode. This permits the length of an RF ablation surface to be varied. Further, the distal end ofthe anvil can be a ground pad electrode.
One or more sensors can be incorporated at the cannula distal end and in the retaining member and its distal end. The retaining member can have a hollow central lumen with one or more fluid distribution ports. A visualization apparatus can be positioned in the lumen. An eyepiece is coupled to the visualization apparatus at a proximal end ofthe cannula.
A flushing port can be formed in the cannula lumen. The flushing port is positioned near a distal end ofthe visualization apparatus in order to introduce a flushing medium past visualization apparatus distal end.
βPJEF PESCRPTTON OF THE FIGURES Figure 1(a) is a perspective view ofthe tissue ablation apparatus ofthe present invention, including a retaining member that is in the form of an anvil.
Figure 1(b) is a perspective view ofthe retaining member which is in the form of a basket or net. Figure 1(c) is a perspective view ofthe retaining member which is in the form of a pair of graspers.
Figure 1(d) is a perspective view ofthe tissue ablation apparatus ofthe present invention, including a rotatable retaining member coupled to a vacuum source.
Figure 2 is a perspective view ofthe cannula with a needle electrode or antenna and a retaining member that is in the form of an anvil.
Figure 3 is a perspective view ofthe distal end ofthe cannula and an energy delivery device extending beyond the cannula's distal end, establishing an optical length.
Figure 4 is a perspective view of a distal end ofthe cannula, with a thermal sensor and an anvil.
Figure 5 is a perspective view ofthe apparatus ofthe present invention with a handle. Figure 6 is an exploded view ofthe retaining member and the cannula.
Figure 7 is a perspective view of a flushing port or optic port associated with the retaining member.
Figure 8 is a block diagram illustrating the inclusion of a controller, power source and other electronic components ofthe present invention. Figure 9 is a block diagram illustrating an analog amplifier, analog multiplexer and microprocessor used with the present invention.
DETAILED DESCRIPTION Referring now to Figure 1(a), a soft tissue ablation apparatus 10 includes a cannula 12, a cannula distal end 12', a cannula proximal end 12" and a cannula lumen 12'". A retaining member 14 is coupled to cannula 12 and extends beyond distal end 12'. Retaining member 14 has a distal end 14' that extends in a lateral direction relative to a longitudinal axis of retaining member 14. Distal end 14' is adapted to capture, receive and retain a tissue ablation target during the ablation process.
A variety of different tissues can be ablated, included but not limited to soft, hard, and mucosal tissue, as well as cartilage. The present invention is particularly suitable in ablating soft palate tissue for purposes of ablation and effecting a cure for snoring. The uvula can be retained by retaining member 14 as one or more energy delivery devices are advanced and retracted out ofthe uvula. Once the desired level of uvula ablation is achieved, retaining member 14 can be rotated, retracted in order to provide a straight shot for energy delivery devices to be introduced into tissue that does not require retainment during ablation.
Retaining member 14 can be fastened with a fastener 16, including but not limited to a ground adjustment nut, and to the body of cannula 12. Alternatively, retaining member 14 can be integrally formed with cannula 12. A retaining member proximal end 14" can include a flushing port 14"' that is adapted to receive a flushing medium.
Retaining member 14 can have a variety of different geometries such as an anvil (Figure 1(a)), a net or basket (Figure 1(b)), a grasper (Figure 1(c)), and the like. Retaining member 14 physically retains and constrains the movement of a targeted ablation tissue before, during and after ablation
Shrink insulation may be provided around the section of retaining member 14 that is adjacent to fastener 16.
One or more energy delivery devices 18 are positioned in lumen 12'". Energy delivery devices 16 can be advanced out of distal end 12* and introduced into the selected tissue target. Alternatively, energy delivery devices 16 can remain stationary in lumen 12'". Cannula 12 is advanced and retracted in order to introduce and retract energy delivery devices 18 in and out ofthe soft palate tissue. Energy delivery devices 18 can be of many varieties, including but not limited to an RF electrode 18 coupled to an RF energy source, a laser optical fiber 18 coupled to a laser source, a microwave antenna 18, and the like. Energy delivery devices 18 can have a sharpened distal end in order to pierce the targeted ablation tissue. A suitable RF electrode 18 is a needle electrode. A deployment and retraction device 20 can be used to advance and retract energy delivery source 18 in and out of distal end 12' and the targeted ablation tissue. Deployment and retraction device 20 includes one or more actuators 20' that are mechanically coupled to energy delivery devices 18. Actuators 20' can be a variety of different knobs and the like that are hand activated. Actuators 20' can be positioned on an exterior surface of a handle 22 and moved axially, along gradation marks 20" to advance or retract. Gradation marks 20" provide an indication of, (i) the extension length of energy delivery devices 18 or (ii) the length of energy delivery devices 18 that is an ablation surface. Other movements of actuators 20' are suitable as long as they provide the appropriate advancement and retraction of energy delivery devices 18.
In one embodiment, retainer member provides for the retention ofthe uvula upon the application of a vacuum, Figure 1(d). In a vacuum source 21 extends to retainer member 14. The soft palate tissue, including but not limited to the uvula, is positioned within an interior of retainer member 14. Vacuum is applied and the soft palate tissue is retained. With the soft palate tissue retained, electromagnetic energy delivery device is introduced into the soft palate tissue. Alternatively, upon application of vacuum, the electromagnetic energy delivery device can include a geometry that at least partially surrounds an exterior ofthe soft palate tissue. Electromagnetic energy is then applied to an exterior ofthe soft palate.
A handle 22 includes a distal end 22' and a proximal end 22". Cannula 12 can be at least partially positioned in handle 22, or at least coupled to distal end
22'. In certain instances, cannula 12 also extends past proximal end 22". A multi- plug 24 extends from proximal end 22", out of an adapter 26 coupled to proximal end 22" or out of proximal end 12". Multi-plug 24 receives a variety of different cables or lines that are coupled to sensors 36, energy delivery devices 18 and other devices. For example, multi-plug 24 can receive lines coupled to,
(i) sensors 36, (ii) an RF electrode 18, (iii) a laser optical fiber 18 or (iv) a microwave antenna 18. Further, a light source cable 30 can be coupled to handle 22, adaptor 26 or distal end 12'.
Energy delivery device 18 can remain in a fixed position relative to cannula 12. In this instance, cannula 12 itself is advanced and retracted from distal end 22' in order to introduce and retract energy delivery devices 18 in and out ofthe targeted ablation tissue. An eyepiece can be coupled at a proximal end of soft tissue ablation apparatus, e.g., to proximal end 22", proximal end 12' or adaptor 26.
Figure 2 more fully illustrates distal end 12'. A visualization apparatus 32 is positioned in lumen 12'" and can be positioned adjacent to energy delivery device 18. As shown, visualization apparatus extends to distal end 12'. It will be appreciated that visualization apparatus can be slideably positioned in lumen 12'" and advance beyond distal end 12'. Further, visualization apparatus 32 can be retained in lumen 12'" and cannula 12 can itself be advanced causing visualization apparatus 32 to move. Visualization apparatus 32 includes optics, an illumination source such as a plurality of optical fibers, and the like, as is well known to those skilled in the art.
As shown in Figure 3, when energy delivery device 18 is advanced from distal end 12' an optical path length is established. It is within this optical path length that visualization is established. After the uvula has first received a topical anesthetic, energy delivery device 18 is introduced into the uvula. A suitable topical anesthetic includes but is not limited to lidocaine and can be administered out of an aperture formed in retaining member 14, cannula 12, and the like. The ablation ofthe targeted tissue is under full visualization. Distal end 14' holds the uvula in place as the lidocaine is sprayed and energy delivery device 18 introduced.
Referring now to Figure 4, an insulation layer 34 is positioned around the exterior of energy delivery device 18 when it is an RF electrode. A slideable insulation layer 34 surrounds electrode 12. In one embodiment insulation 34 can comprise a polyimide material, a thermal sensor 36 positioned on top ofthe polyimide insulation, and a .002 inch shrink wrap. The polyimide insulating layer is semi-rigid. Sensor 36 can lay down substantially the entire length ofthe polyimide.
Figure 5 illustrates the mechanical attachment of deployment apparatus 20 with energy delivery device (RF electrode 18'). Further, handle 22 is more readily adapted to be held as a trigger. An actuator 20"' is positioned at the exterior of handle 22 and is advancement back and forth along gradation marks 20" to adjust the length of insulation layer 34 that covers RF electrode 18'. This provides a variable area of RF electrode 18' that serves as the RF energy ablation surface.
Referring now to Figure 6, retaining member 14 can be removed completely away from cannula 12. This permits soft tissue ablation apparatus 10 to be used in a variety of soft tissue applications besides the uvula, including but not limited to other soft palate structures, the turbinates and the like. Alternatively, retaining member 14 is slightly rotated and withdrawn past distal end 12'.
Referring now to Figure 7, a flushing aperture 38 is included in retaining member 14 to spray a flushing medium across visualization apparatus 32, particularly the optics, in order to clean visualization apparatus 32. This provides a clean view ofthe site. Additionally, a flushing aperture can be included in distal end 12'. One or more thermal sensors 36 can be positioned at distal end 14', at distal end 12', at a distal end of energy delivery device 18, as well as other positions to measure temperature and determine when sufficient energy has been applied to the soft tissue.
Sensors 36 provide temperature measurement and monitoring ofthe target to be ablated and permit a desired level of ablation to be achieved without necrosing too much tissue. This reduces damage to surrounding tissue. By monitoring the temperature at a central point within the interior ofthe selected mass, a determination can be made when ablation is complete. If at any time sensor 36 determines that a desired ablation temperature is exceeded, then an appropriate feedback signal is received at the energy source which then regulates the amount of power delivered to energy delivery device 18. By monitoring temperature, power delivery can be accelerated to a predetermined or desired level. In the case of RF energy, impedance is used to monitor voltage and current. The readings of sensors 36 regulate voltage and current that is delivered to the tissue site. The output for these sensors 36 is used by a controller, described further in this disclosure, to control the delivery of energy to the tissue site. Resources, which can be hardware and/or software, are connected with the thermal sensors 36, the power source and to energy delivery device 18. The resources provide an output for delivering and maintaining a selected energy delivery device 18. Further the resources provide an output that maintains a selected RF energy for a selected length of time. If RF energy is used, the resources are associated with sensors 36, a ground pad electrode (if included) as well as the RF power source for maintaining a selected power at RF electrode 18 independent of changes in voltage or current. Sensors
36 are of conventional design, including but not limited to thermistors, thermocouple, resistive wires, and the like.
Suitable thermal sensors 36 include a T type thermocouple with copper constantene, J type, E type, K type, thermistors, fiber optics, resistive wires, thermocouple IR detectors, and the like. It will be appreciated that sensors 36 need not be thermal sensors.
The following discussion pertains particularly to the use of an RF energy source and RF electrode 18. It will be appreciated that devices similar to those associated with RF electrode 18 can be utilized with laser optical fibers, microwave devices and the like.
Referring now to Figure 8 current delivered through RF electrode 18 is measured by current sensor 42. Voltage is measured by voltage sensor 44. Impedance and power are then calculated at power and impedance calculation device 46. These values can then be displayed at user interface and display 48. Signals representative of power and impedance values are received by controller
50.
A control signal is generated by controller 50 that is proportional to the difference between an actual measured value, and a desired value. The control signal is used by power circuits 52 to adjust the power output in an appropriate amount in order to maintain the desired power delivered at the respective RF electrode 18.
In a similar manner, temperatures detected at the thermal sensors 36 provide feedback for maintaining a selected power. The actual temperatures are measured at temperature measurement device 54, and the temperatures are displayed at user interface and display 48. A control signal is generated by controller 50 that is proportional to the difference between an actual measured temperature, and a desired temperature. The control signal is used by power circuits 52 to adjust the power output in an appropriate amount in order to maintain the desired temperature delivered at the respective sensor.
Controller 50 can be a digital or analog controller, or a computer with software. When controller 50 is a computer it can include a CPU coupled through a system bus. On this system can be a keyboard, a disk drive, or other non-volatile memory systems, a display, and other peripherals, as are known in the art. Also coupled to the bus are a program memory and a data memory.
User interface and display 48 includes operator controls and a display. Controller 50 can be coupled to imaging systems, including but not limited to ultrasound, CT scanners and the like.
Current and voltage are used to calculate impedance. Diagnostics can be performed optically, with ultrasound, CT scanning, and the like. Diagnostics are performed either before, during and after treatment.
The output of current sensor 42 and voltage sensor 44 are used by controller 50 to maintain the selected power level at RF electrode 18. The amount of RF energy delivered controls the amount of power. A profile of power delivered can be incorporated in controller 50, and a pre-set amount of energy to be delivered can also be profiled.
Circuitry, software and feedback to controller 50 result in process control, and the maintenance ofthe selected power that is independent of changes in voltage or current, and are used to change, (i) the selected power, including RF, microwave, laser and the like, (ii) the duty cycle (on-off and wattage), (iii) bipolar energy delivery and (iv) fluid delivery, including flow rate and pressure. These process variables are controlled and varied, while maintaining the desired delivery of power independent of changes in voltage or current, based on temperatures monitored at the thermal sensors 36.
Referring now to Figure 9, current sensor 42 and voltage sensor 44 are connected to the input of an analog amplifier 56. Analog amplifier 56 can be a conventional differential amplifier circuit for use with the thermal sensors 36. The output of analog amplifier 56 is sequentially connected by an analog multipexer 58 to the input of A/D converter 60. The output of analog amplifier 56 is a voltage which represents the respective sensed temperatures. Digitized amplifier output voltages are supplied by A/D converter 60 to a microprocessor 62. Microprocessor 62 may be a model no. 68HCII available from Motorola. However, it will be appreciated that any suitable microprocessor or general purpose digital or analog computer can be used to calculate impedance or temperature.
Microprocessor 62 sequentially receives and stores digital representations of impedance and temperature. Each digital value received by microprocessor 62 corresponds to different temperatures and impedances.
Calculated power and impedance values can be indicated on user interface and display 48. Alternatively, or in addition to the numerical indication of power or impedance, calculated impedance and power values can be compared by microprocessor 62 with power and impedance limits. When the values exceed predetermined power or impedance values, a warning can be given on user interface and display 48, and additionally, the delivery of RF energy can be reduced, modified or interrupted. A control signal from microprocessor 62 can modify the power level supplied by power source 64.
An imaging system can be used to first define the volume ofthe targeted ablation tissue that will be ablated. Suitable imaging systems include but are not limited to, ultrasound, CT scanning, X-ray film, X-ray fluoroscope, magnetic resonance imaging, electromagnetic imaging and the like. The use of such devices to define a volume of a tissue mass or a tumor is well know to those skilled in the art.
Specifically with ultrasound, an ultrasound transducer transmits ultrasound energy into a region of interest in a patient's body. The ultrasound energy is reflected by different organs and different tissue types. Reflected energy is sensed by the transducer, and the resulting electrical signal is processed to provide an image ofthe region of interest. In this way, the volume to be ablated is ascertained.
The foregoing description of a preferred embodiment ofthe 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 ofthe invention be defined by the following claims and their equivalents. What is claimed is:

Claims

1. An ablation apparatus, comprising: a cannula including a distal end, a proximal end and a lumen; a retainer member coupled to the cannula and extending beyond the cannula distal end, the retainer member including a distal end that extends in a lateral direction relative to a retainer member longitudinal axis and adapted to physically retain a selected ablation tissue target; one or more energy delivery devices at least partially positioned in the cannula and capable of being advanced and retracted in and out the cannula distal end; and a deployment and retraction apparatus at least partially positioned in the cannula to deploy and retract the energy delivery device in and out ofthe selected ablation tissue target.
2. The apparatus of claim 1, wherein the retainer member is an anvil.
3. The apparatus of claim 1, wherein the retainer member has a distal end with a net geometry.
4. The apparatus of claim 1, wherein the retainer member has a grasper distal end.
5. The apparatus of claim 1, wherein the retainer member has a hook distal end.
6. The apparatus of claim 1, wherein the energy delivery device is an RF electrode.
7. The apparatus of claim 1, wherein the energy delivery device is laser optical fiber.
8. The apparatus of claim 6, further comprising: an insulator in a surrounding relationship to the RF electrode, the insulator and the RF electrode being slideably engaged to vary a length of RF electrode not covered by the insulator and define an RF electrode ablation surface.
9. The apparatus of claim 1, further comprising: one or more sensors positioned at a distal end of one ofthe cannula or the retaining member.
10. The apparatus of claim 1, wherein the retaining member includes a hollow lumen.
11. The apparatus of claim 1, wherein the retaining member distal end includes one or more fluid distribution ports.
12. The apparatus of claim 1, further comprising: a visualization apparatus with a distal end, the visualization apparatus positioned in a lumen formed in the cannula.
13. The apparatus of claim 12, wherein the visualization apparatus distal end is positioned at the cannula distal end.
14. The apparatus of claim 12, further comprising: an eyepiece coupled to the visualization apparatus and positioned at the proximal end ofthe cannula.
15. The apparatus of claim 1, wherein the retaining member is formed as an integral part ofthe cannula.
16. The apparatus of claim 1, wherein the retaining member is an element that is not an integral part ofthe cannula.
17. The apparatus of claim 1 , wherein a length of the retaining member is adjustable.
18. The apparatus of claim 1, wherein the retaining member distal end is a ground pad electrode.
19. The apparatus of claim 1, further comprising: a handle positioned at the cannula proximal end.
20. The apparatus of claim 12, further comprising: a flushing port formed in the retaining member to deliver a flushing medium directed past the visualization apparatus distal end.
21. The apparatus of claim 1 , wherein the retaining member is slideably mounted to the cannula.
22. The apparatus of claim 1, further comprising: a flushing channel foimed in the cannula lumen, positioned adjacent to the lumen housing the visualization apparatus.
23. The apparatus of claim 1, wherein the retaining member distal end is rotatable.
24. The apparatus of claim 1, wherein the retaining member is retractable in a direction towards the cannula proximal end.
25. The apparatus of claim 1, wherein the retaining member is a hollow lumen coupled to a vacuum source.
26. A soft palate ablation system, comprising: a handle with a distal end and a proximal end; a cannula including a distal end, a proximal end coupled to the handle distal end, and a lumen; a soft palate retaining member coupled to the cannula distal end and extending beyond the cannula distal end, the soft palate retaining member including a distal end that extends in a lateral direction relative to a soft palate retaining member longitudinal axis to retain a selected soft palate tissue to be ablated; an energy delivery device with a distal end that is capable of extending beyond the distal end ofthe cannula; an energy source; and a cable coupling the energy source to the energy delivery device.
27. The system of claim 26, further comprising: a deployment and retraction apparatus at least partially positioned in the cannula to deploy and retract the energy delivery device in and out ofthe selected ablation tissue.
28. The system of claim 26, wherein the retainer member is an anvil.
29. The system of claim 26, wherein the retainer member has a distal end with a net geometry.
30. The system of claim 26, wherein the retainer member has a grasper distal end.
31. The system of claim 26, wherein the retainer member has a hook distal end.
32. The system of claim 26, wherein the energy delivery device is an RF electrode.
33. The system of claim 26, wherein the energy delivery device is laser optical fiber.
34. The system of claim 32, further comprising: an insulator in a surrounding relationship to the RF electrode, the insulator and the RF electrode being slideably engaged to vary a length of RF electrode not covered by the insulator and define an RF electrode ablation surface.
35. The system of claim 26, further comprising: one or more sensors positioned at a distal end of one ofthe cannula or the retaining member.
36. The system of claim 26, wherein the retaining member includes a hollow lumen.
37. The system of claim 26, wherein the retaining member distal end includes one or more fluid distribution ports.
38. The system of claim 26, further comprising: a visualization apparatus with a distal end, the visualization apparatus positioned in a lumen formed in the cannula.
39. The system of claim 38, wherein the visualization apparatus distal end is positioned at the cannula distal end.
40. The system of claim 26, wherein a length ofthe retaining member is adjustable.
41. The system of claim 26, wherein the retaining member distal end is rotatable.
42. The system of claim 26, wherein the retaining member is retractable in a direction towards the cannula proximal end.
43. The system of claim 26, wherein the retaining member is a hollow lumen coupled to a vacuum source.
44. The system of claim 35, further comprising: resources connected with the sensors, the retaining member and the energy source, the resources providing an output for delivering and maintaining a selected energy at the energy delivery device.
45. The apparatus of claim 44, wherein the resources provides an output that maintains a selected energy at the energy delivery device for a selected length of time.
46. An ablation apparatus, comprising: a cannula including a distal end and a proximal end; a vacuum assisted retainer device coupled to the cannula distal end, the retainer member including a uvula receiving member configured to retain at least a portion ofthe uvula with the application of vacuum; an electromagnetic electrode coupled to an electromagnetic energy source; and a vacuum source coupled to the uvula receiving member.
47. The apparatus of claim 46, wherein the electromagnetic electrode is at least partially positioned in an interior ofthe uvula receiving member.
48. The apparatus of claim 46, wherein the electromagnetic electrode is coupled to the distal end ofthe cannula.
49. The apparatus of claim 46, wherein the electromagnetic electrode is at least partially positioned in a lumen ofthe cannula.
50. The apparatus of claim 46, wherein the uvula receiving member is has a closed bottom end and an open top end for receiving the uvula.
51. The apparatus of claim 46, wherein the electromagnetic electrode includes a laterally deflectable distal end relative to a longitudinal axis ofthe electromagnetic electrode.
52. The apparatus of claim 46, wherein an electromagnetic electrode has a geometry configured to surround at least a portion of an exterior ofthe uvula.
53. The apparatus of claim 46, wherein the electromagnetic electrode includes a thermal sensor.
54. The apparatus of claim 53, wherein the thermal sensor is positioned at a distal end ofthe electromagnetic electrode.
55. The apparatus of claim 46, wherein the uvula receiving member includes a thermal sensor.
56. The apparatus of claim 46, wherein the uvula receiving member includes a thermal sensor positioned on an exterior surface ofthe uvula receiving member.
57. The apparatus of claim 46, wherein the electromagnetic electrode is an RF electrode coupled to an RF energy source.
58. The apparatus of claim 57, further comprising: an insulator in at least a partially surrounding relationship to the RF electrode.
59. The apparatus of claim 46, wherein the uvula receiving member includes a fluid distribution port.
60. The apparatus of claim 46, further comprising: a visualization apparatus including a distal end extending to the uvula receiving member.
61. The apparatus of claim 46, further comprising: an eyepiece coupled to the visualization apparatus and positioned at the proximal end ofthe cannula.
62. A method of ablating a portion of a uvula, comprising: providing an ablation apparatus including a cannula, a vacuum assisted retainer device coupled to the cannula distal end, the retainer member including a uvula receiving member configured to retain at least a portion ofthe uvula with the application of a vacuum, and an electromagnetic electrode; introducing at least a portion of a uvula in the uvula receiving member; applying a vacuum to the uvula and retain the uvula in the uvula receiving member applying electromagnetic energy from the electrode to the uvula in the uvula receiving member; and forming an ablation lesion within the uvula.
63. The method of claim 62, wherein the electrode is an RF electrode coupled to an RF energy source.
64. The method of claim 63, wherein the RF ablation electrode is a needle electrode.
65. The method of claim 63, wherein the RF ablation apparatus operates in a bipolar mode.
66. The method of claim 63, wherein the RF ablation apparatus operates in a monopolar mode.
PCT/US1996/013189 1995-08-18 1996-08-16 Ablation apparatus and system for removal of soft palate tissue WO1997006738A1 (en)

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US08/516,781 US5674191A (en) 1994-05-09 1995-08-18 Ablation apparatus and system for removal of soft palate tissue

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NL1003812C2 (en) 1997-07-02

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