GUIDING SHEATH WITH PRESSURE RELIEF CHANNEL

Abstract

A medical device including an elongated tubular body having opposed proximal and distal end portions and defining a longitudinal axis, the elongated tubular body including an interior lumen extending therethrough, wherein an inner surface of the interior lumen includes at least one longitudinal depression formed therein, configured to provide pressure relief to accommodate movement of a medical device passing through the interior lumen.

Claims

1. A medical device comprising: an elongated tubular body having opposed proximal and distal end portions and defining a longitudinal axis, the elongated tubular body including an interior lumen extending therethrough, wherein an inner surface of the interior lumen includes at least one longitudinal depression formed therein, configured to provide pressure relief to accommodate movement of a medical device passing through the interior lumen.

2. The medical device of claim 1, wherein the at least one depression includes a channel extending parallel to the longitudinal axis.

3. The medical device of claim 2, wherein the channel extends between the proximal and distal end portions of the body.

4. The medical device of claim 2, wherein the channel extends to either a proximal end opening of the interior lumen or a distal end opening of the interior lumen.

5. The medical device of claim 2, wherein the channel does not extend to either a proximal end opening of the interior lumen or to a distal end opening of the interior lumen.

6. The medical device of claim 1, further comprising a pull wire lumen embedded within a wall of the tubular body.

7. The medical device of claim 6, wherein an outlet of the pull wire lumen that extends into the interior lumen is located longitudinally beyond a proximal end of the at least one longitudinal depression or a distal end of the at least one longitudinal depression.

8. The medical device of claim 6, wherein the pull wire lumen is in fluid communication with a pull-wire port.

9. The medical device of claim 1, wherein the tubular body includes an inner sheath wall and an outer layer.

10. The medical device of claim 9, wherein the inner sheath wall includes a lubricious material.

11. The medical device of claim 9, wherein the outer layer includes biocompatible polymers.

12. The medical device of claim 11, wherein a steel braid or coil is embedded between the inner sheath wall and the outer layer.

13. The device of claim 9, wherein the inner sheath wall includes the at least one depression on an inner surface thereof.

14. The device of claim 9, wherein the outer layer includes a smooth outer surface defining the outer surface of the tubular body.

15. The device of claim 1, wherein the at least one depression is a straight line extending along the longitudinal axis.

16. The device of claim 1, wherein the at least one depression includes multiple isolated depressions.

17. The device of claim 1, wherein the at least one depression includes multiple depths.

18. The device of claim 1, wherein the at least one depression has a variable width as a function of position along the longitudinal axis.

19. A device comprising: a tubular body having open proximal and distal end portions and defining a longitudinal axis, the tubular body including an interior lumen extending therethrough, wherein an inner surface of the interior lumen has an elongated channel formed therein; and a wire lumen formed within the tubular body, wherein an outlet of the wire lumen extends into the interior lumen and is located longitudinally beyond an end of the channel.

20. The device of claim 19, wherein a lubricious material portion of the tubular body includes the channel.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

[0011] 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:

[0012] FIG. 1 is a perspective view of a sheath according to the disclosure;

[0013] FIG. 2 is a cross-sectional side elevation view of the sheath of FIG. 1, showing the interior of the sheath; and

[0014] FIG. 3 is a cross-sectional front view of the sheath of FIG. 1, showing a depth of a pressure relief channel.

DETAILED DESCRIPTION OF PREFERRED EMBODIMENTS

[0015] 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 FIG. 1 and is designated generally by reference character 100. Other embodiments of the sheath in accordance with the invention, or aspects thereof, are provided in FIGS. 2-3, as will be described.

[0016] FIG. 1 shows an implantable sheath 100. The sheath 100 includes an elongated tubular body 102 having an open proximal end 104 and an open distal end 106. The distal end 106 is inserted into the body. The sheath 100 can include either a straight tip at the distal end 106, a tip with a fixed curve of certain shape depending on the desired target location, or a deflectable tip version, allowing easy navigation and maneuverability throughout the vascular system. The proximal end 104 can be used with a hemostatic valve, allowing a user to introduce other devices into the sheath 100 through the hemostatic valve. Examples of such hemostatic valves are disclosed in U.S. Pat. No. 7,192,433 to Osypka, U.S. Pat. No. 9,572,957 to Osypka, and U.S. Pat. No. 8,137,317 to Osypka, the disclosures of which are incorporated herein by reference in their entireties.

[0017] Referring further to FIG. 1, the sheath 100 is elongated along longitudinal axis 110. The tubular body 102 includes an interior lumen 112 extending from the proximal end 104 to the distal end 106. The interior lumen 112 is intended to accept stents or artificial aortic valves, or therapies such as electrophysiology catheters, balloon catheters or other application to the desired treatment location inside the heart or vascular system. Since these devices can obstruct the inner surface are of the interior lumen 112, thereby possibly resulting in a suction effect, e.g. from the device passing through the interior lumen 112 acting like a piston, the inner surface of the interior lumen 112 includes at least one depression or channel 114 to provide a pressure release by-pass around the device when the interior lumen is blocked by a delivery device.

[0018] Referring now to FIG. 2, a cross section of the sheath 100 is shown. The channel 114 is shown extending along the longitudinal axis 110. The channel 114 extends part of the way from the proximal end 104 and to the distal end 106, not fully reaching either end 104 or 106. One benefit of the channel 114 not extending all the way to the ends 104, 106 is that the channel 114 can provide a leak path for fluids, e.g., liquid or insufflation gas, to flow out of the body into the operating room. This arrangement is an important aspect for moving items 115 within lumen 112. For example if a balloon is pulled back into the inner diameter of the catheter it will cause a buildup of pressure inside the inner diameters of the catheter's proximal end until the balloon reaches the channel 114 to vent that pressure out the distal tip inside the body.

[0019] Referring further to FIG. 2, a wire lumen 116, with port 120, is also placed within the tubular body 102. The wire lumen 116 is located within the interior of the interior lumen 112, opposite the channel 114. An outlet 118 of the wire lumen 116 into the interior lumen 112 is not located between a proximal 114a and distal ends 114b of the channel 114. The outlet 118 is located longitudinally beyond the proximal end 114a and the distal end 114b of the channel 114.

[0020] 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.

[0021] FIGS. 2 and 3 show the channel 114 extending along a straight line parallel to the longitudinal axis 110. Although a single depth as a function of location along the longitudinal axis 110 is depicted for channel 114, the channel 114 can include multiple depths or a variable depth as a function of position along the longitudinal axis 110. Similarly, although a constant circumferential width as a function of position along the longitudinal axis 110 is shown for the channel 114, the channel 114 can include a variable width, that widens or narrows depending on location along the longitudinal axis 110. The sheath 100 can also include more channels circumferentially separated from the channel 114. The channel 114 can also be discontinuous having multiple sections. The sheath 100 can include multiple channels 114 arranged circumferentially within the inner lumen 112. The channel 114 or channels can have various shapes including circular and elongated, and channels can be arranged in various patterns, including staggered and helical with respect to each other.

[0022] 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.