Abstract: Ablation systems and methods for treating atrial fibrillation utilizing RF energy are provided. The system generally includes a first conductive member having a shape which defines a desired lesion pattern or a portion of a desired lesion pattern, and a second conductive member effective to transmit ablative radiation to the first conductive member. The first conductive member is adapted to be positioned on a first tissue surface, and the second conductive member is adapted to be positioned on a second, opposed tissue surface. In use, ablative radiation is transmitted from the second conductive member through the tissue to the first conductive member to form a lesion having the desired lesion pattern.

Abstract: A method of marking an orientation of a cut specimen of tissue prior to excision thereof from a body includes steps of disposing a tissue-marking probe in the body adjacent the cut specimen, the tissue-marking probe including a tissue-marking tool configured to selectively mark the cut specimen. A surface of the cut specimen is then marked with the tissue-marking tool such that the orientation of the cut specimen within the body is discernable after the cut specimen is excised from the body. The tissue-marking tool may be configured to selectively bow out of and back into a window defined near a distal tip of the probe and the marking step may include a step of selectively bowing the tissue-marking tool out of the window and following the surface of the cut specimen while rotating the probe. The tissue-marking tool may include an RF cutting tool and the marking step may include a step of coagulating or cauterizing a selected portion of the surface of the cut specimen with the RF cutting tool.

Abstract: A guide element is used to guide a cutting device when removing breast tissue. The cutting device may have a tissue collection element for collecting tissue. The tissue collection element may be detachable so that the collection element may be removed independent from the cutting device.

Abstract: A cryotherapy system is provided with multiple cryoprobes, each of which has a shaft with a closed distal end adapted for insertion into a body and conduits for flowing a cryogenic fluid through the shaft to reduce a temperature of the distal end. A source is provided for the cryogenic fluid, and flow-control metering valves are provided in fluid communication with the conduits and source of the cryogenic fluid. A compressor is provided in fluid communication with the conduits of the cryoprobes to define a self-contained fluid system. The flow-control metering valves and the compressor are controlled by a computer processor to provide the desired flows of the cryogenic fluid through the conduits of the self-contained fluid system.

Abstract: The heating treatment device according to the present invention is constituted by a coagulation and incision forceps having a plurality of built-in heating elements, and a device main unit. A forceps identifying section inside the device main unit recognizes the identification of the type of forceps by an identifier, and information for the individual heating elements, and supplies the same to a temperature control and correction section. The temperature control and correction section reads out from a memory the resistance values for controlling required for the respective set temperatures for the respective heating elements, on the basis of this information. A heating setting section sets a resistance value for controlling for the set temperature level, from these resistance values for controlling. The resistance value detecting section calculates the resistance value for the heating elements from the measurement results of an applied power detecting section.

Abstract: An ablation device is described comprising an introducer and an electrode array. The electrode array couples to a distal end of the introducer. The electrode array includes a center member having a distal end configured to penetrate tissue and a plurality of electrodes. Proximal and distal ends of each electrode are relatively fixed. The electrodes are dynamically configurable from a retracted state to a deployed state in which the electrodes form a relatively spherical shape in a tissue volume.

Abstract: Bipolar electrosurgical forceps includes a first electrode attached to a first heat pipe and a second electrode attached to a second heat pipe. The heat pipe can be removably attached to the forceps. The forceps can also include a securing mechanism that secures the removable heat pipes to the device.

Abstract: Various high-strength microwave antenna assemblies are described herein. The microwave antenna has a radiating portion connected by a feedline to a power generating source, e.g., a generator. The antenna is a dipole antenna with the distal end of the radiating portion being tapered and terminating at a tip to allow for direct insertion into tissue. Antenna rigidity comes from placing distal and proximal radiating portions in a pre-stressed state, assembling them via threaded or overlapping joints, or fixedly attaching an inner conductor to the distal portion. The inner conductor is affixed to the distal portion by, e.g., welding, brazing, soldering, or by adhesives. A junction member made from a hard dielectric material, e.g., ceramic, can be placed between the two portions and can have uniform or non-uniform shapes to accommodate varying antenna designs. Electrical chokes may also be used to contain returning currents to the distal end of the antenna.

Abstract: An electrosurgical device for treating a body tissue with a high-frequency power includes an electrode for exposing the body tissue to the high-frequency power for treatment, and a high-frequency cautery power supply having a control circuit that outputs a high-frequency power generator for outputting the high-frequency power to the electrode.

Abstract: A cryosurgical system adapted for treatment of fibroadenomas within the breast of a patient. The system includes cryoprobes and a control system which operates the cryoprobes to accomplish freezing in two stages, including a high power freeze and a low power freeze.

Abstract: An ablation device for cardiac tissue, especially for forming a circular lesion around a vessel orifice in the heart, comprises a steerable catheter that is provided in the region of its distal end with an abutment device for holding the distal end of the catheter on a cardiac vessel orifice; and a linear ablation applicator that is disposed distally or proximally relative to the abutment device of the catheter and can be brought from a straight passive position into a radially expanded, approximately circular-arc-type encircling ablation position.

Abstract: A catheter system and method for selectively cooling or freezing target neuronal tissue to induce lesions along the neuroaxis and produce cryoanalgesia by impairing nerve conduction of the targeted neuronal tissue. The system includes a catheter that has cryogenic capability for variable cooling or freezing of neuronal tissue. The catheter also includes temperature sensing and electrodiagnostic capabilities. A pressurized fluid source is included for inflating a portion of the catheter body. The system includes electrodiagnostic equipment for stimulating and monitoring sensory evoked potentials in the patient. The method involves placement of the catheter tip in the subarachnoid space of the spinal canal and location of the tip on the neuronal target using imaging and electrodiagnostic techniques.

Abstract: An ablation catheter stores a platelet inhibitor substance within a plurality of pockets or recesses of its shaft. The substance is adapted to elute upon contact with biological fluid. In the pocket configuration, the platelet inhibitor substance is in a capsule positioned within the pocket. In the recess configuration, the platelet inhibitor substance is in a hydrogel or silicone-based porous/semi-porous matrix positioned within the recess. Elution of the platelet inhibitor substance prevents or at least substantially minimizes the adhesion of blood platelets on the catheter surface during ablation. In another configuration, the catheter includes an internal lumen network having apertures terminating at the surface of the shaft. The lumen communicates with a source of platelet inhibitor fluid that is forced through the lumen by a variable pump.

Abstract: This invention is a circumferential ablation device assembly which is adapted to form a circumferential conduction block in a pulmonary vein. The assembly generally comprises a handheld surgical ablation probe having a rigid shaft for insertion through a patient's chest and a circumferential ablation element mounted on the distal end portion of the shaft. The circumferential ablation element is adapted to ablate a circumferential region of tissue along a pulmonary vein wall which circumscribes the pulmonary vein lumen. The circumferential ablation element includes an expandable member for anchoring the distal end portion of the shaft in a body structure and an ultrasound transducer disposed within the expandable member for emitting ultrasonic energy to ablate the tissue in the pulmonary vein.

Abstract: An intravascular electrophysiology (EP) device for the mapping and/or formation of lesions along the isthmus region of a heart that has particular utility in the treatment of atrial flutter. The EP device of the invention has an elongated shaft with a proximal section, a compound-curved or modified pigtail-shaped distal section, and a plurality of at least partially exposed electrodes disposed on an outer surface of the distal section. The electrodes are spaced along a length of the distal section and may be interspersed with at least one temperature sensor located between electrodes. The shape of the distal end of the device enables manipulation of the device by inserting its distal end in the tricuspid valve and retracting the device to bias the section having electrodes along the isthmus to achieve acceptable contact with the region so high frequency (e.g., RF) electrical energy delivered to the electrodes on the distal section of the EP device will form a lesion.

Abstract: A light-emitting treatment device including one or more light-emitting elements disposed in a flexible and stretchable pad (or a body-conforming shaped article) defining a skin- or tissue-adhering surface having an inherently tacky characteristic for secure application to the skin, tissue, or other external or internal regions of the patient's body. The light-emitting treatment device is configured to contact and adhere to the skin or tissue of a patient, and irradiate an underlying region for photodynamic therapy. The treatment device may be fabricated from a shell member and a filler material (such as a molded silicone rubber shell member and a silicone gel filler material), to provide a skin-adhering, peelable, washable, and repositionable contact surface.

Abstract: In electrosurgical system includes an electrosurgical generator providing power through an electrode, and a laser providing laser energy through an optical fiber. The electrode optical fiber and a source of environmental gas can all be included in a handpiece, catheter or other delivery device. In operation, the environmental gas can be released into the vicinity of an operative site and the laser activated to energize atoms along a pathway. Electrosurgical power can then be applied to ionize the items of the atoms of the pathway and create a path of least resistance for an electrosurgical arc. A reduction in the laser power required can be achieved by matching the photon frequency of the laser with the excitation frequency of the environmental gas. In a laparoscopic procedure, the insufflation gas may be used as the environmental gas.

Abstract: A plate of biocompatible material is provided having curvature in two planes such that it conforms to the curvature of the L5 vertebral body and to the patient's lordotic curve. Holes are provided receiving screws for anchorage in the vertebral body and sacrum. A flange or foot portion on the plate provides a wider base end area for support in the L5-S1 interspace. The foot portion is also arranged for appropriate entry angle of screws into the sacrum such as to improve anchorage in the sacrum. Anti-backout and low profile features are incorporated. The anterior lumbar plate is situated to maintain the anterior interbody bone graft in compression by resisting tensile forces during extension.

Abstract: A catheter particularly useful for ablation lesions within a tubular region of or near the heart is provided. The catheter comprises an elongated flexible tubular catheter body having an axis and proximal and distal ends. An ablation assembly is mounted at the distal end of the tubular body. The ablation assembly has a preformed generally circular curve having an outer surface and being generally transverse to the axis of the catheter body. The ablation assembly comprises a flexible tubing having proximal and distal ends that carries a tip electrode at its distal end. An electrode lead wire extends through the catheter body and into the ablation assembly and has a distal end connected to the tip electrode. In use the distal end of the catheter is interested into the heart of a patient.

Abstract: A urological resectoscope including a main body carrying a tubular shaft, an optical guide plate arranged at a fixed distance proximally of the main body, a sliding body longitudinally movably guided between the main body and the optical guide plate and a spring bridge comprising two levers connected pivotally together at one end and acted on by a spring, the other ends of which are pivotally connected to the sliding body on the one hand and to the optical guide plate or the main body on the other hand. One of the levers is pivotally connected to only one side of the sliding body.