Abstract: Methods and apparatus for the treatment of a body cavity or lumen are described where a heated fluid and/or gas may be introduced through a catheter and into treatment area within the body contained between one or more inflatable/expandable members. The catheter may also have optional pressure and temperature sensing elements which may allow for control of the pressure and temperature within the treatment zone and also prevent the pressure from exceeding a pressure of the inflatable/expandable members to thereby contain the treatment area between these inflatable/expandable members. Optionally, a chilled, room temperature, or warmed fluid such as water may then be used to rapidly terminate the treatment session.

Abstract: A system for displaying characteristics of target tissue during an ablation procedure is provided that includes an electronic control unit (ECU) configured to receive data regarding electrical properties of the target tissue for a time period. The ECU is also configured to determine a value responsive to the data and indicative of at least one of a predicted depth of a lesion in the target tissue, a predicted temperature of the target tissue, and a likelihood of steam pop of the target tissue for the time period. The system further includes a display device operatively connected to the ECU. The display device is configured to receive the value and display a visual representation indicative of at least one of a predicted depth of a lesion in the target tissue, a predicted temperature of the target tissue, and a likelihood of steam pop of the target tissue for the time period.

Abstract: Methods and apparatus for the treatment of a body cavity or lumen are described where a heated fluid and/or gas may be introduced through a catheter and into treatment area within the body contained between one or more inflatable/expandable members. The catheter may also have optional pressure and temperature sensing elements which may allow for control of the pressure and temperature within the treatment zone and also prevent the pressure from exceeding a pressure of the inflatable/expandable members to thereby contain the treatment area between these inflatable/expandable members. Optionally, a chilled, room temperature, or warmed fluid such as water may then be used to rapidly terminate the treatment session.

Abstract: A console for providing power to a surgical tool. Internal to the console is a power supply that supplies power, a processor that regulates the application of the power and a memory reader that reads data from a memory integral with the tool. The power is sourced over terminals also part of the console. The tool memory data are used to regulate the characteristics of the sourced power. An isolation circuit also internal to the console extends between the terminals over and the memory reader. The isolation circuit allows the memory reader to send read requests to the tool memory and receive data signals from the tool memory over the terminals while protecting the memory reader from the power signals sourced by the power supply.

Abstract: An electrosurgical device: forceps having: a first working arm, a second working arm, wherein the electrosurgical device has a first electrosurgical configuration where the first working arm and the second working arm are in an opposed position so that the forceps deliver a first therapy current that flows between the first working arm and the second working arm; and wherein the electrosurgical device has a second electrosurgical configuration when the first working arm, the second working arm, or both are repositionable relative to each other so that the first working arm is extended with respect to the second working arm or vice versa and a second therapy current is delivered from the first working arm to a remote electrode.

Abstract: Methods and apparatus for the treatment of a body cavity or lumen are described where a heated fluid and/or gas may be introduced through a catheter and into treatment area within the body contained between one or more inflatable/expandable members. The catheter may also have optional pressure and temperature sensing elements which may allow for control of the pressure and temperature within the treatment zone and also prevent the pressure from exceeding a pressure of the inflatable/expandable members to thereby contain the treatment area between these inflatable/expandable members. Optionally, a chilled, room temperature, or warmed fluid such as water may then be used to rapidly terminate the treatment session.

Abstract: An electrosurgical system comprising: a handpiece including: a first working arm, a second working arm, and an activation circuit having a first switch state and a second switch state, wherein a therapy current is conducted between the first working arm and the second working arm when the activation circuit is in the second switch state and the handpiece is in a first position; wherein the therapy current is conducted between the first working arm or the second working arm, and an adjacent handpiece component when the activation circuit is in the second switch state and the handpiece is in a second position; and wherein the therapy current is not conducted when the activation circuit is in the first switch state.

Abstract: A balloon ablation catheter achieves reduction in diameter of the balloon upon balloon contraction and increased reliability of the thermocouple temperature sensor, which balloon ablation catheter is less likely to be influenced by the heating liquid discharged into the balloon and able to control the balloon surface temperature with high accuracy.

Abstract: A method of treating tissue is provided, including positioning a portion of a catheter in proximity to cardiac tissue; measuring an impedance value with the catheter; determining a respiratory rate based at least in part on the measured impedance value; and thermally treating the cardiac tissue with the catheter.

Abstract: A medical device for treating tissue includes a tissue-contacting surface and a solid state heating element that is thermally coupled to the tissue-contacting surface. The solid state heating element is configured to generate heat to thermally treat tissue.

Abstract: A cryoablation system has a catheter that receives working cryogen, the catheter having a catheter body that has a distal section having a freezing element which delivers the working cryogen to a treatment location, and a balloon enclosing the freezing element. The catheter body includes an outer tube that has two delivery tubes and a guide wire tube positioned inside the outer tube.

Abstract: A surgical instrument includes one or more electrically-conductive plates adapted to connect to a source of energy for supplying energy to tissue to treat tissue, a temperature sensing element, and a thermal spread control assembly coupled to the temperature sensing element. The thermal spread control assembly is configured to determine a flow rate of heat energy across the temperature sensing element and to control the energy applied to the electrically-conductive plate and/or control active cooling of the temperature sensing element in accordance with the determined flow rate of heat energy.

Abstract: An electrosurgical instrument is provided for the treatment of tissue, the instrument comprising an instrument shaft (10) having a longitudinal axis, and an electrode assembly at one end of the shaft. The electrode assembly comprises first and second active electrodes (11), (14) and at least one return electrode (25), the electrodes being electrically insulated one from another by means of one or more insulation members (12). The first and second active electrodes (11, 14) each have an exposed surface for treating tissue, the exposed surface (19) of the first active electrode being such as to treat tissue disposed laterally of the longitudinal axis at a first radial position with respect to the instrument shaft. The exposed surface (15) of the second active electrode is such as to treat tissue disposed laterally of the longitudinal axis at a second radial position with respect to the instrument shaft.

Abstract: A surgical instrument comprises: an elongated sheath, an energy probe, an elongated energy conductor, and an elongated cooling member. The energy probe is connected to the distal end portion of the sheath. The elongated energy conductor is contained within the sheath and arranged to transmit distally to the energy probe energy from an energy source. The elongated cooling member is reciprocally movable within the sheath and thermally coupled at its proximal portion to a cooler. The cooling member is movable between a proximal, non-cooling position and a distal, cooling position. In the non-cooling position, a distal end of the cooling member is displaced proximally from the energy probe so as to impede thermal conduction therebetween; in the cooling position, the distal end of the cooling member thermally contacts the energy probe so as to facilitate thermal conduction therebetween.

Abstract: A medical instrument is disclosed. The medical instrument includes a housing and a handle for gripping by a user, an end effector coupled to the handle and having at least one electrical contact, a battery, and a radio frequency (RF) generation circuit coupled to and operated by the battery. The RF generation circuit is operable to generate an RF drive signal and to provide the RF drive signal to the at least one electrical contact, wherein the RF generation circuit is supported by the housing. The RF generation circuit includes a resonant circuit that includes at least one inductive element constructed of litz wire.

Abstract: A medical instrument is disclosed. The medical instrument includes a housing, at least one electrical contact, a radio frequency (RF) generation circuit coupled to and operated by the battery and operable to generate an RF drive signal and to provide the RF drive signal to the at least one electrical contact, and a user interface supported by the housing. The user interface includes visual and audible feedback elements, wherein the state of the instrument can be determined by the state of the visual and audible feedback elements.

Abstract: An electrode is for use in an electrosurgical probe, the electrode having two arms defining a longitudinal direction. The electrode also includes a loop depending from the two arms and defining a cutting area within the loop, and a vaporization member attached to one side of the loop. The vaporization member is such that it does not occlude the cutting area and yet presents a substantial profile when the electrode is moved in the longitudinal direction. The arrangement is such that when the electrode is moved in a first longitudinal direction, the loop is capable of resecting a sample of tissue. When the electrode is moved in the opposite longitudinal direction, the vaporization member is capable of vaporizing tissue adjacent thereto to form a groove therein.

Abstract: Methods and apparatus for the treatment of a body cavity or lumen are described where a heated fluid and/or gas may be introduced through a catheter and into treatment area within the body contained between one or more inflatable/expandable members. The catheter may also have optional pressure and temperature sensing elements which may allow for control of the pressure and temperature within the treatment zone and also prevent the pressure from exceeding a pressure of the inflatable/expandable members to thereby contain the treatment area between these inflatable/expandable members. Optionally, a chilled, room temperature, or warmed fluid such as water may then be used to rapidly terminate the treatment session.

Abstract: A method of cooling a material including the steps of (i) providing a cryotherapy instrument, (ii) positioning a portion of the cryotherapy instrument adjacent the material to be cooled, and (iii) circulating a cryogenic fluid through the cryotherapy instrument under physical conditions near a critical point of a liquid-vapor system for the cryogenic fluid. The critical point defines a point in a phase diagram of the liquid-vapor system where molar volumes are substantially equivalent for liquid and gas, whereby vapor lock associated with cooling of the cryotherapy instrument is avoided.

Abstract: A medical device system and method provide an RF electrosurgical generator coupled to an electrosurgical electrode via a patient box disposed in close proximity to the patient. An RF signal is delivered from the generator to the patient box where signal power is increased and the RF signal delivered to the electrosurgical electrode. The patient box is coupled to the electrosurgical electrode by a short cable capable of carrying an HV, high frequency 5 MHz signal without leakage. An electrical characteristic associated with the electrosurgical electrode is monitored and a desired RF power output and duty cycle maintained by adjusting DC input voltage applied to an RF amplifier, responsive to the monitoring. The system determines when the electrosurgical cutting electrode has started cutting and switches from a start mode to a run mode having a different RF duty cycle and a reduced RF power output controlled by a servo system.