US2005085775A1PendingUtilityA1
Indwelling device
Priority: Feb 14, 2002Filed: Aug 12, 2004Published: Apr 21, 2005
Est. expiryFeb 14, 2022(expired)· nominal 20-yr term from priority
A61B 90/40A61M 25/0017A61N 1/05A61F 2/86A61N 1/056A61M 5/00
39
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Claims
Abstract
A medical device for insertion into a body having a surface covered by a detachable cover. The cover may be detached from the surface and removed from the body while the device is inserted in the body. The device may be, for example, a catheter, cannula, drain, stent, pacemaker, or electrode.
Claims
exact text as granted — not AI-modified1 . A medical device for insertion into a body, the device having at least one surface covered by and attached to at least one detachable cover, the cover being detachable from the surface and removed from the body any time after the device has been inserted in the body, wherein the presence of said cover does not prevent the device from fulfilling its intended function, and wherein said medical device is selected from the group consisting of:
(a) a catheter; (b) a cannula; (c) a drain; (d) a stent; (e) a pacemaker; and (f) an electrode.
2 . The device according to claim 1 , wherein said device is a urinary catheter.
3 . The device according to claim 1 , wherein said device is a venous catheter.
4 . The device according to claim 1 , wherein said device is a dialysis catheter.
5 . The device according to claim 1 , having a stack of at least two sequentially detachable covers, each cover being detachable either from the surface of the device or from the adjacent cover, and removed from the body while the device is within the body.
6 . The device according to claim 5 , wherein the at least two covers are identical.
7 . The device according to claim 1 , wherein the cover is formed from a material selected from the group consisting of:
(a) rubber; (b) silicone rubber; (c) polyvinylchloride; (d) latex; (e) woven metal mesh; (f) parylene; (g) polyurethane; (h) mylar; and (i) nylon.
8 . The device according to claim 1 , wherein the cover is formed from a biocompatible material.
9 . The device according to claim 1 , wherein the cover is formed from a non-allergenic material.
10 . The device according to claim 1 , wherein the cover has a smooth surface.
11 . The device according to claim 1 , wherein the cover has a rough surface.
12 . The device according to claim 5 , containing a pharmaceutical agent between two adjacent covers.
13 . The device according to claim 12 , wherein the pharmaceutical agent is an anti-infective agent.
14 . The device according to claim 13 , wherein the anti-infective agent is an antibiotic drug.
15 . The device according to claim 1 , wherein the cover is reversibly attached to a surface by elastic forces in the cover.
16 . The device according to claim 1 , wherein the cover is detachable from the surface by tearing the cover.
17 . The device according to claim 1 , wherein the cover is tearable along one or more preformed seams or perforations in the cover.
18 . The device according to claim 1 , comprising a blade slidable over the surface so as to cut the cover and detach the cover from the surface.
19 . The device according to claim 1 , further comprising a ring placed at a distal end of the shaft to prevent materials from entering between the cover and the surface.
20 . The device according to claim 1 , wherein the cover comprises an inner cylindrical shell and an outer cylindrical shell, the inner and outer cylindrical shells each having a distal end and a proximal end, the inner and outer cylindrical shells being attached to each other at their proximal ends and at their distal ends.
21 . The device according to claim 1 , comprising one or more balloons located between the cover and the surface, the cover being attached to the surface when the balloons are inflated, and detached from the surface when the balloons are not inflated.
22 . The device according to claim 1 , wherein the cover is impenetrable to microorganisms.
23 . The device according to claim 1 , wherein the cover is impenetrable to water.
24 . The device according to claim 1 any one of the precious claims, wherein the cover stores and releases a substance.
25 . The device according to claim 24 , wherein the substance is an anti-microbial or anti-fungal compound.
26 . The device according to claim 1 , wherein the cover has two parallel rows of perforations or seams separating a strip of the cover, the strip being attached at a distal end to a first end of a cord and a second end of the cord being accessible at a proximal end of the device.
27 . The device according to claim 1 , further comprising a cutter slidable along the surface of the device, the cutter being configured to cut the cover when sliding along the surface.
28 . The device according to claim 1 , wherein the cover has a row of perforations such that when the proximal end of the perforation is torn, the cover may be made to slide over the surface in a proximal direction.
29 . The device according to claim 1 , further comprising a distal sealing tip, wherein said tip is capable of preventing ingress of fluids into the space between the distal end of the cover(s) and the medical device
30 . The device according to claim 29 , wherein the distal sealing tip is made of polyurethane.
31 . The device according to claim 1 , further comprising a proximal sealing element, wherein said element is capable of preventing ingress of fluids into the space between the proximal end of the covers(s) and the medical device.
32 . The device according to claim 1 , further comprising a proximal sealing element, wherein said element is constructed such that it may adopt two distinct conformations, such that when the sealing element is in the first conformation, said element is capable of preventing ingress of fluids into the space between the proximal end of the covers(s) and the medical device, and when the sealing element is in the second position, said element permits easy removal of the outer cover, together with the associated biofilm.
33 . The device according to claim 31 or claim 32 , wherein the proximal sealing element is made of polyurethane.
34 . The device according to claim 1 , further comprising a fixed blade attached to the proximal end of said device, such that said blade is capable of incising the cover, when said cover is pulled proximally toward said blade.
35 . The device according to claim 1 , further comprising a distal sealing element
as defined in claim 29 , a proximal sealing element as defined in claim 31 or claim 32 and a fixed blade as defined in claim 34 .
36 . A method for preventing biofilm buildup on the surface of an indwelling medical device that has been inserted into the body of a subject, said method comprising the steps of:
a) providing a medical device fitted with a detachable cover attached to at least a portion of its outer surface, such that the presence of said cover does not interfere with the intended function of said device; b) inserting said device together with its attached cover into the body of the subject; c) detaching the cover from the outer surface of the medical device and removing said cover from the body together with any biofilm deposited on the surface of said cover, while leaving the device inside the body such that it may continue to fulfill its intended function.
37 . A method for preventing biofilm buildup on the surface of an indwelling medical device that has been inserted into the body of a subject, said method comprising the steps of:
a) providing a medical device fitted with a stack of two or more sequentially detachable covers, such that the innermost cover is attached to at least a portion of its outer surface, and wherein the presence of said stack of covers does not interfere with the intended function of said device; b) inserting said device together with its attached cover into the body of the subject; c) detaching the outermost cover from the stack of sequentially detachable covers and removing said cover from the body together with any biofilm deposited on the outer surface thereof, while leaving the device inside the body such that it may continue to fulfill its intended function; d) subsequently repeating step (c) for the one or more remaining outermost covers.
38 . The method according to claim 36 or claim 37 , wherein the medical device is selected from the group consisting of:
(a) a catheter; (b) a cannula; (c) a drain; (d) a stent; (e) a pacemaker; and (f) an electrode.
39 . The method according to claim 38 , wherein the device is a urinary catheter.
40 . The method according to claim 38 , wherein the device is a venous catheter.
41 . The method according to claim 38 , wherein the device is a dialysis catheter.Join the waitlist — get patent alerts
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