Abstract:
In accordance with one aspect, the invention relates to medical devices which comprise at least one reservoir, a therapeutic-agent-containing region disposed within the reservoir and an electrode comprising a conductive polymer. The devices of the invention are configured such that a rate of release of the therapeutic agent from the reservoir changes upon a change in the oxidation state of the conductive polymer.
Abstract:
A system for protecting a stent includes an electroactive polymer (EAP) sleeve, a stent, a balloon catheter, and a voltage source. A voltage is applied to the EAP sleeve, whereupon the EAP sleeve expands. The stent, disposed about the balloon catheter is inserted into the region defined by the inner surface of the EAP sleeve. The voltage is removed, whereupon the EAP sleeve contracts.
Abstract:
A medical device at least a portion of which has a degradable coating, the coating degrading in an aqueous environment, and to methods of making and using the same. The coating may be a layer-by-layer coating, the first layer comprising a material having a positive charge and the second layer comprising a material having a negative charge.
Abstract:
A catheter assembly comprises a catheter shaft having a proximal region a distal region and a rotational seal therebetween. The rotational seal comprises a first component fixedly engaged to the proximal region and a second component fixedly engaged to the distal region. The components engaged in an overlapping arrangement. The rotational seal is actuatable between a non-activated and activated states. In the non-activated state the first component and the second component are separated by a gap which provides for the distal region of the catheter shaft to be rotatable relative to the proximal region. In the activated state at least a portion of the fist component and the second component being sealingly engaged together such that distal region is made static relative to the proximal region.
Abstract:
A medical device may be secured to a medical device delivery apparatus by providing a wrapped medical device, the wrapped medical device comprising a medical device with a polymeric sheet disposed thereabout, compressing the wrapped medical device and affixing at least one opposing edge of the polymeric sheet to a portion of the polymeric sheet adjacent thereto so as to form a sheathed medical device and securing the sheathed medical device to a medical device delivery apparatus.
Abstract:
A stent can comprise a tubular body having a first region and a second region. The tubular body is defined by a plurality of serpentine bands. Each serpentine band comprises a plurality of alternating proximal turns and distal turns connected by struts. The second region comprises a first serpentine band and a second serpentine band that overlap one another about a common stent circumference. The first region comprises a serpentine band that is not overlapped by another serpentine band about a common stent circumference.
Abstract:
Medical devices, for example, those that have balloons, and methods of making the devices are described. In some embodiments, a method includes providing a medical balloon having a first cone portion and a body portion, and removing material from an outer surface the body portion of the balloon such that the balloon includes a first region and a second region, the first region being recessed relative to the second region.
Abstract:
A catheter assembly adapted to treat a vessel bifurcation. A balloon member of the catheter assembly includes a main body portion and a cylindrical shaped bulge portion that extends radially outward from the main body portion. The bulge portion extends around a circumference of the main body portion. A stent of the catheter assembly is typically mounted to the balloon member. When treating the vessel bifurcation, the catheter assembly is positioned with the bulge portion aligned axially relative to an ostium of the branch vessel. The balloon member is inflated to expand a portion of the stent into the branch vessel. The circumferential construction of the bulge portion of the balloon member reduces the need for radial (rotational) alignment of the balloon member relative to the ostium of the branch vessel.
Abstract:
A post dilatation balloon catheter includes a balloon member having a proximal portion, a distal portion and a circumferential bulge portion. The circumferential bulge portion extends around a circumference of the balloon member and is positioned at a location between the proximal and distal portions of the balloon member. The circumferential bulge portion inflates to a maximum inflated dimension that is greater than a maximum dimension of the proximal and distal portions of the balloon member. The balloon member is arranged into a folded state by folding at least one of the distal and proximal portions of the balloon member in a separate step from folding the circumferential bulge portion.
Abstract:
In accordance with one aspect, the invention relates to medical devices which comprise at least one reservoir, a therapeutic-agent-containing region disposed within the reservoir and an electrode comprising a conductive polymer. The devices of the invention are configured such that a rate of release of the therapeutic agent from the reservoir changes upon a change in the oxidation state of the conductive polymer.