Abstract:
A RF catheter system includes a catheter with a proximal portion, a distal portion having a distal end and a lumen extending from the proximal portion to the distal portion. Inner and outer coaxially aligned conductors extend within the catheter and are coaxial with the lumen. A deflectable catheter guide is disposed within the catheter lumen and extends proximally within the catheter lumen and terminates distally of the distal end of the catheter to define a biological ablation pathway. A radio-frequency antenna is disposed at the distal portion of the catheter and is in electrical communication with the inner and outer coaxially aligned conductors. The radio-frequency antenna is adaptable to receive and transmit radio-frequency energy for ablating biological tissue along the ablation pathway.
Abstract:
The present invention relates to a system adapted to position an ablation catheter at a location where a pulmonary vein extends from an atrium. The system optimally comprises a deflectable guidewire and a sheath. An ablation catheter is disclosed for use with the positioning system, wherein the deflectable guidewire and the sheath cooperate so as to facilitate positioning of the catheter at the location.
Abstract:
The present invention relates to actuators, linear motors and rotational motors based on magnetic-field-induced strains taking place in the actuator material. These strains are caused by the reorientation of the twin structure of the actuator materials by the applied magnetic field.
Abstract:
In a fuse chamber (8) there is arranged as a quenching gas source a burn-off element (11), which concentrically surrounds an arc chamber (10) and is separated from it by a fuse element (9), which consists of metal foil, preferably silver foil, and the outer side of which is adjoined by the burn-off element (11). The latter consists of an igniting material (12), arranged in the form of a ring running around centrally, and a gas-evolving material (13). Both materials consist, for example, of guanidine or guanidine derivatives as the combustible material and an oxidant, the proportion of which in the igniting material (12) is hyperstoichiometric. The arc chamber (10) is bounded at opposite ends by nozzles (7a,b), which connect it to exhaust volumes (4a,b). When there is an overcurrent, the fuse element (9) heats up to the igniting temperature of the igniting material (12) and is torn open centrally. The arc forming is axially blown by the quenching gas, which forms during the burning-off of the burn-off element (11), and quenched. The fuse element (9) may centrally have a triggering zone, where it is more easily interruptible, in particular meltable. The quenching gas source may also comprise compressed-gas tanks or cold-gas generators.
Abstract:
Improved electrode assemblies for treating a tissue region at or near a sphincter comprise a support structure and an electrode carried by the support structure for advancement in a path to penetrate the tissue region. In one arrangement, the electrode has a non-cylindrical cross section selected to resist deflection when advanced to penetrate the tissue region. In another arrangement, the electrode includes a tissue stop to resist tissue penetration beyond a selected depth. In another arrangement, the electrode includes a proximal portion formed from a first material and a distal tissue penetrating portion formed of a second material different than the first material. The first material can comprise, e.g., stainless steel, and the second material can comprise, e.g., nickel titanium.
Abstract:
An electrode catheter is introduced into a vein or other hollow anatomical structure, and is positioned at a treatment: site within the structure. The end of the catheter is positioned near a junction formed in the structure. This junction can be the sapheno-femoral junction. The position of the catheter near the junction is determined based on a signal from a device associated with the catheter within the structure. A fiber optic filament which emits light is used with the catheter or a guide wire over which the catheter is advanced. The light is visible externally from the patient. The light dims and may no longer externally visible at the sapheno-femoral junction where the catheter moves past the deep fascia and toward the deep venous system. The position of the catheter can be determined based on this external observation. The position of the catheter can also be determined based on measured parameters such as temperature or flow rate within the structure, and the measured changes in one or more of these parameters as the catheter nears the junction. The hollow anatomical structure can be compressed for this procedure. The position of the catheter can also be determined mechanically by including a hook-shaped tip on the catheter or guide wire which would physically engage the junction.
Abstract:
An invention directed to the partial or whole disassembly of products. An article includes a first and second portion fastened together by a releasable fastener device. The releasable fastener device includes shape memory material and is in the form of a female element threadedly engaged with a complementary male element through a first threaded engagement region of the shape memory material provided on one of the elements and a second threaded engagement region provided on the other element. The releasable fastener device is operative upon shape transition to change the cross-sectional shape of the first threaded engagement region to radially move the first threaded engagement region clear of the second threaded engagement region so as to release the threaded engagement between the male and female elements and leave the male element free to withdraw from the female element without having to be unscrewed therefrom.
Abstract:
A method of treating a tumor includes providing a tissue biopsy and treatment apparatus that includes an elongated delivery device that has a lumen and is maneuverable in tissue. A sensor array having a plurality of resilient members is deployable from the elongated delivery device. At least one of the plurality of resilient members is positionable in the elongated delivery device in a compacted state and deployable with curvature into tissue from the elongated delivery device in a deployed state. At least one of the plurality of resilient members includes at least one of a sensor, a tissue piercing distal end or a lumen. The sensor array has a geometric configuration adapted to volumetrically sample tissue at a tissue site to differentiate or identify tissue at the tissue site. At least one energy delivery device is coupled to one of the sensor array, at least one of the plurality of resilient members or the elongated delivery device. The apparatus is then introduced into a target tissue site. The sensor array is then utilized to distinguish a tissue type. The tissue type information derived from the sensor array is utilized to position the energy delivery device to ablate a tumor volume. Energy is then delivered from the energy delivery device to ablate or necrose at least a portion of the tumor volume. The sensor array is then utilized to determine an amount of tumor volume ablation.
Abstract:
An embodiment of the invention provides a tissue biopsy and treatment apparatus that comprises an elongated delivery device that is positionable in tissue and includes a lumen. A sensor array having a plurality of resilient members is deployable from the elongated delivery device. At least one of the plurality of resilient members is positionable in the elongated delivery device in a compacted state and deployable with curvature into tissue from the elongated delivery device in a deployed state. At least one of the plurality of resilient members includes at least one of a sensor, a tissue piercing distal end or a lumen. The sensor array has a geometric configuration adapted to volumetrically sample tissue at a tissue site to differentiate or identify tissue at the target tissue site. At least one energy delivery device is coupled to one of the sensor array, at least one of the plurality of resilient members or the elongated delivery device.
Abstract:
A catheter assembly having a sheath, which includes a side wall enclosing an interior bore, and a distal region. The assembly also has a bendable catheter tube, which is carried for sliding movement in the interior bore. A pull wire also runs through the interior bore of the sheath, preferably within a lumen. The catheter tube has a distal portion with a coupling which joins the distal portion of the catheter tube and the distal portion of the pull wire. Relative movement of the pull wire and the sheath causes bending of the catheter tube outwardly through the opening, in response to sliding movement of the catheter tube within the interior bore toward the distal region of the sheath.