Abstract: The vasoocclusive device for use in interventional therapy and vascular surgery adapted to be inserted into a portion of a vasculature, includes a vasoocclusive coil disposed about an inner reinforcement coil wherein said vasoocclusive coil is helically wound and the inner reinforcement coil forms a reverse helical winding opposite the vasoocclusive coil winding, thereby forming a biplex wound coil. The vasoocclusive device biplex winding provides improved mechanical properties to the device. An inner reinforcement stretch resistant member attached within the biplex windings limits coil stretchability.

Abstract: The present invention is directed to an implantable vascular prosthesis configured for use in a wide range of applications, such as treating aneurysms, maintaining patency in a vessel, and providing controlled delivery of therapeutic agents to a vessel wall. The prosthesis comprises a helical body having a plurality of turns, wherein the proximal and distal edges of the turns of the prosthesis has a pattern that interdigitates when the prosthesis assumes the deployed configuration. The prosthesis optionally may comprise a radially expanding distal portion coupled to the helical body for facilitating placement of the prosthesis within a body vessel.

Abstract: An implantable vascular prosthesis having improved flexibility is provided comprising a helical body portion having a reduced delivery configuration and an expanded deployed configuration, the helical body portion comprising a plurality of cells interconnected by hinge points that enhances flexibility of the vascular prosthesis and provides at least partial nesting of adjacent turns of the helical body portion in the reduced delivery configuration.

Abstract: The present invention is directed to a prosthesis for treating an aneurysm, and delivery systems and methods therefor. The prosthesis includes a radially expanding distal section coupled to a helical section, the helical section including a localized feature configured to exclude or retard blood flow into an aneurysm. Methods of loading the prosthesis onto a specially-designed delivery system that facilitates proper orientation of the prosthesis within a target vessel, and methods of using the delivery system to deliver the prosthesis, also are provided.

Abstract: The present invention is directed to a delivery system for delivering a vascular prosthesis within a vessel, the vascular prosthesis having a contracted delivery configuration and a deployed configuration. The delivery system comprises a loader tube having a lumen preloaded with a delivery wire carrying a vascular prosthesis in the contracted delivery configuration. A separately inserted sheath includes a lumen configured to accept the vascular prosthesis, while retaining it in the contracted delivery configuration. The delivery wire is used to translate the vascular prosthesis to a distal end of the sheath for deployment in a vessel.

Abstract: This invention relates generally to vasoocclusive devices, and more particularly concerns a vasoocclusive device that has a first elongated, reduced friction configuration in which the vasoocclusive device may be deployed through a catheter or cannula to an anatomical cavity at a site in the vasculature to be treated. The device has a second configuration assumed at the site to be treated which consists of a component that creates an anchor in the adjacent vasculature and a component for framing or filling the anatomical cavity.

Abstract: A vasoocclusive coil is reinforced with a stretch resistant member to improve safety during retraction of the coil. The stretch resistant member is fixedly attached at one end to the vasoocclusive coil, and the other end of the stretch resistant member is detachably mounted to an elongated pusher member to allow for placement and release of the vasoocclusive coil within the patient's vasculature. The stretch resistant member may be formed from a therapeutic and/or bioactive non-metallic material to enhance the therapeutic properties of the vasoocclusive coil.

Abstract: An implantable vascular prosthesis having improved flexibility is provided comprising a helical body portion having a reduced delivery configuration and an expanded deployed configuration, the helical body portion comprising a plurality of cells interconnected by hinge points that enhances flexibility of the vascular prosthesis in the reduced delivery configuration.

Abstract: The introducer sheath can be loaded onto a vasoocclusive device after removal of the vasoocclusive device from a microcatheter, to permit the vasoocclusive embolic coil assembly to be used again during a clinical procedure. The sheath includes a hollow, elongated tubular member with a longitudinal slot formed in the upper wall of the elongated tubular member and extending along the length of elongated tubular member. The upper wall of the elongated tubular member adjacent to the slot has an angled configuration to accept the vasoocclusive device. The sheath may include wing members extending outwardly from the angled configuration on the outside surface of the hollow, elongated tubular member to facilitate insertion of the vasoocclusive device into the sheath. The elongated tubular member may also consist of a segment with no slot attached to a flexible pusher member to facilitate initiation of loading of the vasoocclusive device into the sheath.

Abstract: The introducer sheath can be loaded onto a vasoocclusive device after removal of the vasoocclusive device from a microcatheter, to permit the vasoocclusive embolic coil assembly to be used again during a clinical procedure. The sheath includes a hollow, elongated tubular member with a longitudinal slot formed in the upper wall of the elongated tubular member and extending along the length of elongated tubular member. The upper wall of the elongated tubular member adjacent to the slot has an angled configuration to accept the vasoocclusive device. The sheath may include wing members extending outwardly from the angled configuration on the outside surface of the hollow, elongated tubular member to facilitate insertion of the vasoocclusive device into the sheath. The elongated tubular member may also consist of a segment with no slot attached to a flexible pusher member to facilitate initiation of loading of the vasoocclusive device into the sheath.

Abstract: A vasoocclusive coil is reinforced with a stretch resistant member to improve safety during retraction of the coil. The stretch resistant member is fixedly attached at one end to the vasoocclusive coil, and the other end of the stretch resistant member is detachably mounted to an elongated pusher member to allow for placement and release of the vasoocclusive coil within the patient's vasculature.

Abstract: The introducer sheath can be loaded onto a vasoocclusive device after removal of the vasoocclusive device from a microcatheter, to permit the vasoocclusive embolic coil assembly to be used again during a clinical procedure. The sheath includes a hollow, elongated tubular member with a longitudinal slot formed in the upper wall of the elongated tubular member and extending along the length of elongated tubular member. The upper wall of the elongated tubular member adjacent to the slot has an angled configuration to accept the vasoocclusive device. The sheath may include wing members extending outwardly from the angled configuration on the outside surface of the hollow, elongated tubular member to facilitate insertion of the vasoocclusive device into the sheath. The elongated tubular member may also consist of a segment with no slot attached to a flexible pusher member to facilitate initiation of loading of the vasoocclusive device into the sheath.

Abstract: A stent or stent-graft deployment apparatus or mechanism configured so that, when activated, the stent or stent-graft progressively expands in a direction from its end which is proximally positioned to the deployment instrument, such as a percutaneous catheter, to its end which is distally positioned to the deployment instrument. The stent or stent-graft deployment mechanism includes a tether or slip line configuration which reduces the likelihood of snagging between the line and stent member. A method is also provided for deploying a stent or stent-graft within a mammalian lumen which includes expanding the stent or stent-graft in such a proximal-to-distal direction. The apparatus and method of the present invention minimize the likelihood of the stent or stent-graft from being displaced from the desired site before it is somewhat secured in the vessel during deployment.

Abstract: A stent or stent-graft deployment apparatus or mechanism configured so that, when activated, the stent or stent-graft progressively expands in a direction from its end which is proximally positioned to the deployment instrument, such as a percutaneous catheter, to its end which is distally positioned to the deployment instrument. The stent or stent-graft deployment mechanism includes a tether or slip line configuration which reduces the likelihood of snagging between the line and stent member. A method is also provided for deploying a stent or stent-graft within a mammalian lumen which includes expanding the stent or stent-graft in such a proximal-to-distal direction. The apparatus and method of the present invention minimize the likelihood of the stent or stent-graft from being displaced from the desired site before it is somewhat secured in the vessel during deployment.

Abstract: This invention relates to a novel two-stage heat recovery submerged combustion heating system. More particularly, this invention relates to a novel submerged combustion heating system with a lowered self-cooling combustion chamber and a two stage heat recovery system. The system can be installed singly or in combination with other similar submerged combustion systems to heat large quantities of liquids and liquid-solid solutions.

Abstract: This invention relates to a novel two-stage heat recovery submerged combustion heating system. More particularly, this invention relates to a novel submerged combustion heating system with a lowered self-cooling combustion chamber and a two stage heat recovery system. The system can be installed singly or in combination with other similar submerged combustion systems to heat large quantities of liquids and liquid-solid solutions.

Abstract: A composition is provided that provides a nutritionally complete, calorically-dense formulation suitable for use as a supplement or total enteral feeding. The composition is specifically tailored to meet the requirements of hepatic patients in need of nutritional support. In contrast to current hepatic formulas, the composition is ready-to-use and does not require reconstitution and admixing. The ready-to-use formula contains a protein source that contains at least 25% of its total protein content as free crystalline amino acids.