290 results about "Body conduit" patented technology

A catheter is adapted to exchange heat with a body fluid, such as blood, flowing in a body conduit, such as a blood vessel. The catheter includes a shaft with a heat exchange region disposed at its distal end. This region may include hollow fibers which are adapted to receive a remotely cooled heat exchange fluid preferably flowing in a direction counter to that of the body fluid. The hollow fibers enhance the surface area of contact, as well as the mixing of both the heat exchange fluid and the body fluid. The catheter can be positioned to produce hypothermia in a selective area of the body or alternatively positioned to systemically cool the entire body system.

A catheter is adapted to exchange heat with a body fluid, such as blood, flowing in a body conduit, such as a blood vessel. The catheter includes a shaft with a heat exchange region disposed at its distal end. This region may include at least one balloon which is adapted to receive a remotely cooled heat exchange fluid preferably flowing in a direction counter to that of the body fluid. Embodiments including multiple balloons enhance the surface area of contact, and the mixing of both the heat exchange and the body fluid. The catheter can be positioned to produce hypothermia in a selective area of the body without cooling the entire body system. It is of particular advantage in brain surgeries where stroke, trauma or cryogenic tumors can best be addressed under hypothermic conditions.

A constraining sheath for use around an endoprosthesis (e.g., a stent device, with or without a graft covering), which may be a balloon expandable endoprosthesis but more preferably is a self-expanding prosthesis. The endoprosthesis is coaxially enclosed within and substantially covered by the constraining sheath, which is an outer, removable tubular sheath, preferably made of ePTFE. The sheath is preferably corrugated circumferentially along at least a portion of the length of the endoprosthesis. The constraining sheath and endoprosthesis are preferably mounted together as an assembly at the distal end of a delivery means such as a catheter shaft, for delivery of the endoprosthesis to a desired location within a body conduit such as an artery. The constraining sheath is removed by the application of tension to a tensile member such as a tether to cause sequential pulling out of the corrugations followed by release and deployment of the endoprosthesis. The use of a corrugated constraining sheath in comparison to a non-corrugated sheath results in a more smoothly applied tensile force to effect the endoprosthesis release as well as requiring less maximum force.

A surgical clamp includes opposing jaws and a covering enhancing traction between the jaws and a body conduit. A multiplicity of fibers oriented to extend longitudinally between the clamp and conduit may be composed of filaments and either woven or non-woven to form a fabric. A variety of weaves are contemplated to provide different textures, each having its own traction characteristics. The nature of the weave can control characteristics such as smoothness, absorption, and texture. The fibers or filaments may be formed from any solid or semi-solid material, adding its own characteristics to the resulting fabric insert or clamp.

A device and method for treating bodily conduits involves the application of energy to the smooth muscle tissue of the conduit walls to reduce the bulk of smooth muscle tissue and mucus glands. The irradiation treatment of the smooth muscle tissue causes a reduction in the amount of smooth muscle tissue over time which increases the inner diameter of the body conduit for improved fluid flow and prevents smooth muscle spasms. The treatment is particularly useful in the lungs for treatment of asthma to prevent bronchospasms, increase the airway diameter for improved air exchange, and reduce mucus secretions in the lungs.

A surgical clip assembly is provided having two molded components and a tension spring. In one aspect of the invention, the spring clip includes a first molded portion having a first jaw and a first finger tab, a second molded portion coupled to the first molded portion and having a second jaw and a second finger tab, and a tension spring coupled to both the first and second molded portions. The first and second molded portions may be identical components and are moveable by operation of the first and second finger tabs between a generally closed position and a generally open position. The finger tabs may include cavities or grooves to facilitate engagement with a user or the jaws of a clip applier. The jaws may be shaped, curved or bent to provide access to specific areas of a procedure. Each of the jaws can be provided with an insert to further reduce trauma and increase traction with a target body conduit In a preferred process of assembling the clip, the tension spring is wound at least one turn forming a central coil and two extensions, and each of the molded portions is formed with a hinge area. Each of the hinge areas includes a hinge stud and a hinge cavity. The hinge areas operate to align and snap-fit with one another to form the clip assembly. With the assembly process of the invention, the extensions of the tension spring may be mounted into guide slots or ribs of either the jaws or finger tabs of the molded portions. A feature of the present invention is different tension springs having various strength and tension properties may be used in accordance with the needs and requirements of each surgical procedure without changing the construction of the molded portions.

A male compression-type coaxial cable connector having an adapter nut attached to a leading end of a tubular connector body portion. The connector body portion has a first axial conduit with a barbed ferrule coaxially mounted therein. The connector further comprises a compression sleeve having a second axial conduit slidingly disposed over a trailing end of the tubular connector body portion. A deformable compression ring is removably disposed within the second axial conduit. In use, the prepared end of the coaxial cable is inserted through the compression sleeve and compression ring and advanced into the connector body conduit until it can be advanced no further. Subsequent advancement of the compression sleeve over the connector body portion, with the assistance of a compression tool, forces the deformable trailing end of the compression ring radially inward to compress the cable jacket and braid thereby providing secure attachment of the connector to the cable. The compression ring is removable and can be replaced with another compression ring having a different inner diameter to accommodate a variety of coaxial cables. The construction permits the compression sleeve to be easily removed for replacing the compression ring and easily reinstalled over the connector body after ring replacement.

The present invention is directed to bioabsorbable self-expanding medical devices for use inside or outside body conduits that self-expand at, or below, normal human body temperature without requisite for a polymeric thermal transition

An access device adapted for use in a body conduit is provided comprising an outer tube having a proximal end and a distal end, an inner tube disposed coaxially with the outer tube having a proximal end and a distal end, and an expandable portion having a first end coupled to the distal end of the outer tube and a second end coupled to the distal end of the inner tube. The outer tube and the inner tube are movable relative to each other to transform the expandable portion between a low-profile state and a high-profile state, and at least one of the outer and inner tubes comprises a wire-reinforced tube or is formed from a plurality of individual, discrete, generally ring-shaped elements arranged in series and fused or bonded together to form a continuous tubular structure. The access device may further comprise an actuator coupled to one of the outer and inner tubes and being movable relative to the other of the outer and inner tubes to transform the expandable portion between the low- and high-profile states. The expandable portion may be formed with a braid material and has the shape of a cone. The ring-shaped elements may be formed of a thermoplastic or a thermoset material, and they may include at least one of plastic rings, metallic rings, un-reinforced plastic rings and metal reinforced plastic rings assembled along the length of at least one of the tubes to provide variable flexibility and kink-resistance. The wire-reinforced tube is formed by coating a wire with a plastic material, wrapping the coated wire around a mandrel forming a plurality of windings, and heating the wound coated wire until the plastic material melts and bonds the windings forming the wire-reinforced tube.

A catheter facilitating traversal of restrictions in body conduits includes a shaft having a distal tip with a shape that is non-conical, radially twisted, and rectangular in radial cross section. An outer surface of the tip includes at least one side section extending from a blunt point radially outwardly with progressive positions proximally along an axis of the tip. The side section includes a proximal portion in proximity to the shaft, and a distal portion twisted radially with respect to the proximal portion. The catheter can be adapted for placement over a guidewire and can be made transparent thereby facilitating visualization through an endoscope in the catheter.

The present invention comprises systems, methods and devices for the delivery of compositions for occluding or of means for opening conduits. The implantable occlusive material may be delivered pre-formed or in situ cured and, may be a resorbable material that supports tissue ingrowth that eventually replaces the material leaving little or no original material in place. The delivery system is positioned to allow for placement of the occlusive material into the body conduit. Use of delivery systems, methods and devices for re-opening an occluded body conduit are also included.

An implantable access port for use in transferring fluid transdermally between an external fluid storage or dispensing device and a site within a patient is disclosed. The access port includes a body, at least two reservoirs defined within the access port body, and at least one septum secured to the body and enclosing the reservoirs within the body. The access port also includes reservoir outlets defined within the reservoirs. The access port also has body conduits defined within the body and in fluid communication with the reservoir outlets and external openings defined in the exterior of the body. An implantable access port and system for use in apheresis is also provided that includes an implantable access port, at least one needle, and a catheter that is fluidly connected to the access port.

A removable device such as a stent-graft, intended for applications where it may be desirable to remove the device at some time following implantation. The stent-graft of the present invention includes a helically-wound stent component provided with a covering of graft material. It is removable by gripping an end of the helically-wound stent component with a retrieval device and applying tension to the stent component in the direction in which it is intended to be withdrawn from the site of implantation. The use of such a retrieval device allows the stent-graft to be removed remotely, such as via a catheter inserted into the body at a different location from the implantation site. The design of the stent-graft is such that the stent component is extended axially while the adjacent portion of the graft separates between windings of the stent component. The axial extension of the stent component, with portions of the graft still joined to the stent component, allows the device to be “unraveled” (or “unwound”) and removed through a catheter of diameter adequately small to be inserted into the body cavity that contained the stent-graft. It is removed atraumatically, without incurring significant trauma to the body conduit in which it had been deployed.

A catheter is adapted to exchange heat with a body fluid, such as blood, flowing in a body conduit, such as a blood vessel. The catheter includes a shaft with a heat exchange region disposed at its distal end. This region may include at least one balloon which is adapted to receive a remotely cooled heat exchange fluid preferably flowing in a direction counter to that of the body fluid. Embodiments including multiple balloons enhance the surface area of contact, and the mixing of both the heat exchange and the body fluid. The catheter can be positioned to produce hypothermia in a selective area of the body without cooling the entire body system. It is of particular advantage in brain surgeries where stroke, trauma or cryogenic tumors can best be addressed under hypothermic conditions. Heat pipe technology can be used to form a heat pipe heat exchange catheter. The heat pipe heat exchange catheter includes metallic bellows which allow for flexibility. The temperature control source can be portable to enable the heat pipe heat exchange catheter to be used in the ambulatory environment.

A catheter device that is useable to extract material from a body conduit, such as a blood vessel, comprises a flexible catheter advanceable into the body conduit, an opening in the wall of the catheter that is in fluid communication with a material collection chamber, and a controllably arcuate segment along the catheter shaft, near the distal tip of the catheter and including the opening. Further said catheter may include a sliding member, located within a lumen of the catheter, that is used to move the material entering the catheter through the arcuate segment opening, into the material collection chamber and away from said opening. The catheter may include a single mechanism utilized to both generate a vacuum to cause material to enter the catheter at the arcuate segment opening and also cause the sliding member to travel, inside the catheter, moving material away from the opening and into the material collection chamber. Methods of utilizing such a catheter device to remove material from a body conduit are also disclosed.

A thin-wall PTFE (polytetrafluoroethylene) tube in the form of a tube of porous expanded PTFE film wherein the porous PTFE film has a microstructure containing a multiplicity of fibrils. The thin-wall tube is used in a non-porous embodiment as the balloon portion of a balloon catheter. The thin-wall tube is not elastomeric; however, because of the thinness, strength and flexibility of the tube, it may be inserted into a body conduit in a collapsed state and then deployed from a catheter and inflated up to the maximum diameter of the thin-wall tube. The porous PTFE film is provided with a continuous layer of adhesive to provide the non-porous tube; the adhesive is preferably a thermoplastic and more preferably a thermoplastic fluoropolymer such as fluorinated ethylene propylene.

A catheter adapted to increase the patency of a body conduit includes an elongate tube having an axis extending between a proximal end and a distal end, and a balloon disposed at the distal end of the tube and having properties for being expanded to a high-profile state and for being contracted to a low-profile state. A sleeve disposed over the balloon has a pair of ends disposed on opposing sides of a central section, the ends having a floating relationship relative to the tube with the central section disposed circumferentially of the balloon. An electrode disposed outwardly of the sleeve has properties for being electrosurgically energized to incise materials defining the body conduit when the balloon is in the high-profile state. The electrode can be formed of a plurality of elements stranded to increase the surface area of the electrode. The catheter can be inserted relative to a guide member having a conductor which carries the electrosurgical energy from the proximal end of the tube to the electrode at the distal end of the tube. An associated method includes the step of introducing electrosurgical energy into the conductor of the guide member to energize the electrode of the catheter.

A drainage catheter is adapted to drain fluid from the body cavity through a body conduit and includes an elongate tube having a distal end and a retention member disposed at the distal end and adapted for movement between the low-profile state facilitating insertion of the catheter and a high-profile state facilitating the tension of the catheter in its operative position. A woven mesh forms at least a portion of one of the tube and the retention member, and can be made permeable or impermeable in various regions of the catheter. The woven mesh can be formed of filaments heat-settable so that the catheter automatically moves to the high-profile state. Insertion of the catheter can be facilitated using an obturator and a guidewire in an associated method, an obturator facilitating insertion of the catheter can be removed to permit the catheter to automatically return to a normal, high-profile state.

An implantable blood pressure regulator is provided. The blood pressure regulator includes at least one connection zone and an attenuation zone. The connection zone is suitable for connection to a body conduit, such as a blood vessel. The attenuation zone is movable from a first state to a second state in response to a physiological pressure spikes. The movement from the first state to the second state lowers a level of pressure or dampens a pressure spike in the body conduit.

A stent is adapted for disposition in a body conduit of a patient and comprises a mesh formed in the configuration of a tube and having an axis and axial convolutions, which facilitate movement between a low-profile state and a high-profile state. The tube in the low-profile state has an elongate configuration and a wall with a first thickness and first tube strength. The tube in the high-profile state has a compressed configuration and a wall with a second thickness greater than the first thickness and a second hoop strength greater than the first hoop strength. An associated method of use includes the steps of mounting the step on a catheter between first and second enlargement members, increasing the size of the enlargement members, and moving the enlargement members to axially compress the stent to the high-profile state. An associated method of manufacture includes the steps of corrugating the mesh on a mandrel by moving the ends of the mesh toward each other. The mesh can then be heat-set in the high-profile state.