Abstract:
A biostable polymeric substrate of an implantable medical device unit includes a demand-release bioactive composition including one or more bioactive agents covalently bound to surface-modifying end groups of the substrate. Certain cellular activities, in proximity to the polymeric substrate, release substances reacting with the end groups such that the end groups release the one or more bioactive agents, which modify the certain cellular activities.
Abstract:
A system and method for positioning an implantable medical device IMD 10 within a living body is disclosed. The IMD includes a flow-directed member 35 that is deployed within the body to carry the IMD via the flow of blood. The flow-directed member 35 may be an inflatable member such as a balloon, or a mechanical member such as a parachute structure that deploys within the body. The IMD further includes a pressure measuring device 32 and a pressure monitor 30 to obtain pressure measurement at one or more locations within the body adjacent the IMD. The pressure measurements are used to estimate the location of at least a portion of the IMD relative to the body to aid in positioning the IMD in the body without the use of a fluoro-visible media.
Abstract:
A system and method for positioning an implantable medical device (IMD) within a living body is disclosed. The IMD includes a flow-directed member that is deployed within the body to carry the IMD via the flow of blood. The flow-directed member may be an inflatable member such as a balloon, or a mechanical member such as a parachute structure that deploys within the body. The IMD further includes a pressure measuring device and a pressure monitor to obtain pressure measurement at one or more locations within the body adjacent the IMD. The pressure measurements are used to estimate the location of at least a portion of the IMD relative to the body to aid in positioning the IMD in the body without the use of a fluoro-visible media.
Abstract:
An implantable lead (10) for establishing electrical contact between a medical device and body tissue, in which an active fixation mechanism (18) secures the lead (10) in place while allowing a distal electrode (14) on the lead to mechanically "float" with respect to the body tissue. In one embodiment, the active fixation mechanism (18) comprises a curved hook disposed on the lead (10) at a point spaced proximally back from the distal end (14) of the lead (10). The curved hook (18) defines a helix around at least a portion of the lead's circumference. A hollow introducer needle is slidably disposed on the lead (10). The hollow needle is provided with a longitudinal slit in a distal section of its length, such that the distal section of the needle can be advanced over the distal end (14) the lead (10), past the fixation hook, which is received in the longitudinal slit. With the needle slid over the distal end (14) of the lead (10), the needle is stabbed tangentially into an implant site, bringing the fixation hook (18) proximal to the surface of the body tissue. Then, the needle is twisted (bringing about a twisting of the lead (10)), causing the curved fixation hook (18) to pierce and engage the body tissue, securing the lead (10) in place. Then the needle is withdrawn from the body tissue and removed from the lead (10). In an alternative embodiment, the lead (10) can be placed by an endocardial approach using a flexible cannula with a longitudinally slotted tip.
Abstract:
A small diameter, unipolar or bipolar, atrial or ventricular transvenous or epimyocardial pacing lead with a porous, platinized, steroid eluting cathode electrode exhibiting an effective surface area in the range of 0.1 to 4.0 mm , preferably 0.6 to 3.0 mm , provides low stimulation thresholds in the range of 0.5 volts, 0.5 milliseconds, very high pacing impedance (800 to 2,000 OMEGA ), relatively low polarization, good to excellent sensing, and adequately low source impedance. The high pacing impedance prolongs the longevity of pacing pulse generators and allows for the miniaturization of their components. The low thresholds allow large safety factors at low applied voltages, which also contribute to increased battery longevity.
Abstract:
The present invention provides delivery systems for delivering conduction protein genetic material to cardiac cells in localized areas of the heart to improve the conductance therein. More specifically, there is provided a system for delivering connexin proteins or nucleic acid molecules encoding connexin proteins to a site in the heart which has been determined by mapping procedures to have a conduction disturbance. For cases where conduction is impaired, selected genetic material is delivered by Applicants' delivery system to cells around the disturbance area, in order to enhance overall conductivity patterns; in other cases, genetic material is selected to slow conduction in affected areas, so as to prevent, e.g., brady-tachy syndrome.