The subject invention is directed to an introducer or guiding sheath catheter, and more particularly, to an introducer or guiding sheath catheter for delivering a device, such as a balloon catheter, stent or other device.
Introducer systems and guiding sheaths are commonly used to introduce and guide medical devices and applications to a desired location inside the human vascular system. These devices commonly have a concentric round through-lumen, with a tapered distal tip for easy insertion into the vascular system, and a proximal end with a hemostatic valve, allowing the user to introduce other devices into the sheath from the proximal side through a hemostatic valve. The system typically includes sheaths to deliver other medical devices, such as stents or artificial aortic valves, or therapies such as electrophysiology catheters, balloon catheters, or other applications to the desired treatment location inside the heart or vascular system. Often such devices are complex in shape and expand throughout the inner lumen, and the complete inner diameter of the sheath, possibly resulting in a suction effect, making it difficult to move the device inside the sheath diameter.
The traditional systems and methods have been considered sufficient for their intended purposes. However, there is a need in the art for an improved sheath construction, at least to decrease resultant suction effects during insertion. The subject invention provides a solution to this need.
A medical device includes an elongated tubular body having opposed proximal end and distal end portions and defining a longitudinal axis. The elongated tubular body includes an interior lumen extending therethrough. An inner surface of the interior lumen includes at least one channel therein configured to provide pressure relief for movement of a medical devise passing through the interior lumen.
The at least one channel can extend parallel to the longitudinal axis. The channel can extend between the proximal end and the distal end portions, can extend to either a proximal end opening of the interior lumen or a distal end opening of the interior lumen, and need not extend to either the proximal end opening of the interior lumen or to the distal end opening of the interior lumen.
The medical device can also include a pull wire lumen embedded within a wall of the tubular body. An outlet of the pull wire lumen into the interior lumen can be located longitudinally beyond a proximal end of the at least one depression and a distal end of the at least one depression. The pull wire lumen can be in fluid communication with a pull-wire port.
The tubular body can include an inner sheath wall and an outer layer. The inner sheath wall can include a lubricious material. The outer layer can include biocompatible polymers and a stainless steel braid or coil, where the steel braid or coil is embedded between the inner sheath wall and the outer layer. The inner sheath wall can include the at least one depression on an inner surface thereof. The outer layer can include a smooth outer surface defining the outer surface of the tubular body.
The depression can follow a straight line extending parallel to the longitudinal axis. It is also conceived that the at least one depression can include multiple isolated depressions or sections. The depression can include multiple depths and the channel can have a variable width as a function of position along the longitudinal axis.
These and other features of the systems and methods of the subject disclosure will become more readily apparent to those skilled in the art from the following detailed description of the preferred embodiments taken in conjunction with the drawings.
So that those skilled in the art to which the subject invention appertains will readily understand how to make and use the devices and methods of the subject invention without undue experimentation, preferred embodiments thereof will be described in detail herein below with reference to certain figures, wherein:
Reference will now be made to the drawings wherein like reference numerals identify similar structural features or aspects of the subject invention. For purposes of explanation and illustration, and not limitation, a partial view of an exemplary embodiment of an implantable sheath in accordance with the invention is shown in
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The sheath 100 is made up of an inner layer 122 and an outer layer 124. The inner layer 122 includes an inner sheath made up of partially a lubricious material, such as such as PTFE, FEP or Nylon, allowing the introduced devices 115 to be moved and pushed easily through the through-lumen, while the outer layer 124 includes biocompatible polymers, such as such as Nylons, PEBEX, Polyurethanes of various durometers. A reinforcing steel braid or coil 126 is embedded between the inner sheath wall 122 and the outer layer 124. The channel 114 is defined within the inner layer 122, while the outer layer 124 includes a smooth inner surface and a smooth outer surface.
The methods and systems of the present disclosure, as described above and shown in the drawings, provide for an improved sheath, having the ability to relieve pressure build up from blockage and suction effects as devices traverse the inner lumen. While the apparatus and methods of the subject disclosure have been shown and described with reference to embodiments, those skilled in the art will readily appreciate that changes and/or modifications may be made thereto without departing from the spirit and score of the subject disclosure.
The subject application claims the benefit of priority to U.S. Provisional Patent Application Ser. No. 63/077,337, which was filed on Sep. 11, 2020, the contents of which are incorporated by reference herein in its entirety.
Number | Date | Country | |
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63077337 | Sep 2020 | US |