US20060122709A1 - Prosthesis intended for the treatment of a natural lumen or tract, in particular an endo-urethral prosthesis - Google Patents

Prosthesis intended for the treatment of a natural lumen or tract, in particular an endo-urethral prosthesis Download PDF

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US20060122709A1
US20060122709A1 US11338818 US33881806A US2006122709A1 US 20060122709 A1 US20060122709 A1 US 20060122709A1 US 11338818 US11338818 US 11338818 US 33881806 A US33881806 A US 33881806A US 2006122709 A1 US2006122709 A1 US 2006122709A1
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prosthesis
element
tubular
sphincter
fig
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US11338818
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Marian Devonec
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Devonec Marian A
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    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61FFILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, E.G. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F2/00Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
    • A61F2/82Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61FFILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, E.G. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F2/00Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
    • A61F2/02Prostheses implantable into the body
    • A61F2/04Hollow or tubular parts of organs, e.g. bladders, tracheae, bronchi or bile ducts
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61FFILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, E.G. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F2/00Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
    • A61F2/02Prostheses implantable into the body
    • A61F2/04Hollow or tubular parts of organs, e.g. bladders, tracheae, bronchi or bile ducts
    • A61F2002/047Urethrae
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61FFILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, E.G. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F2210/00Particular material properties of prostheses classified in groups A61F2/00 - A61F2/26 or A61F2/82 or A61F9/00 or A61F11/00 or subgroups thereof
    • A61F2210/0004Particular material properties of prostheses classified in groups A61F2/00 - A61F2/26 or A61F2/82 or A61F9/00 or A61F11/00 or subgroups thereof bioabsorbable
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61FFILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, E.G. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F2250/00Special features of prostheses classified in groups A61F2/00 - A61F2/26 or A61F2/82 or A61F9/00 or A61F11/00 or subgroups thereof
    • A61F2250/0014Special features of prostheses classified in groups A61F2/00 - A61F2/26 or A61F2/82 or A61F9/00 or A61F11/00 or subgroups thereof having different values of a given property or geometrical feature, e.g. mechanical property or material property, at different locations within the same prosthesis
    • A61F2250/0039Special features of prostheses classified in groups A61F2/00 - A61F2/26 or A61F2/82 or A61F9/00 or A61F11/00 or subgroups thereof having different values of a given property or geometrical feature, e.g. mechanical property or material property, at different locations within the same prosthesis differing in diameter
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61FFILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, E.G. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F2250/00Special features of prostheses classified in groups A61F2/00 - A61F2/26 or A61F2/82 or A61F9/00 or A61F11/00 or subgroups thereof
    • A61F2250/0058Additional features; Implant or prostheses properties not otherwise provided for
    • A61F2250/0067Means for introducing or releasing pharmaceutical products into the body

Abstract

A prosthesis intended for the treatment of a natural lumen or tract of a human or animal body through which a flow is effected on either side of a sphincter is disclosed. The prosthesis comprises at least one tubular element, in particular of cylindrical shape which is sufficiently flexible to conform to the natural lumen, but sufficiently rigid to maintain an artificial passage in the lumen, and is intended to be placed in the natural lumen. The wall of the tubular element comprises a relatively smooth and soft biocompatible material, such as silicone rubber, at least in its outer part.

Description

    CROSS-REFERENCE TO RELATED APPLICATIONS
  • [0001]
    This is a Continuation of U.S. application Ser. No. 10/447,110 filed May 29, 2003, which is a Continuation of U.S. application Ser. No. 09/899,112 filed Jul. 6, 2001 (now U.S. Pat. No. 6,576,008), which is a Continuation-in-Part of U.S. application Ser. No. 09/032,978 filed Mar. 2, 1998 (now U.S. Pat. No. 6,290,666), which is a Division of U.S. application Ser. No. 08/501,140 (now U.S. Pat. No. 5,766,209), which a National Stage application of PCT/FR/94/00171 filed Feb. 16, 1994. The entire disclosure of the prior applications is hereby incorporated by reference herein in its entirety.
  • BACKGROUND
  • [0002]
    The present invention relates to the treatment of natural lumina or tracts of the human or animal body through which a transit or flow of a fluid is effected, in particular a body fluid, either liquid or gaseous, on either side of a sphincter. The urinary, respiratory, digestive, and gynecological tracts constitute natural lumina within the meaning of the present invention.
  • [0003]
    “Treatment” is understood to mean both an intervention of a mechanical type, aiming to re-establish a flow which has previously been disturbed or prevented on account of an obstruction or a stenosis of the natural lumen, and also a treatment or intervention with a therapeutic objective, for example, to control the cicatrization of the wall of the natural lumen after surgical intervention, or to reduce hyperplasia of an organ or gland surrounding this same lumen.
  • [0004]
    The present invention will be introduced, defined and described, by way of a non-limiting example, with reference to the endo-urethral prostheses which are used in the urethra in connection with the striated muscular sphincter.
  • [0005]
    In accordance with the document FR-A-2 667 783, an endo-urethral prosthesis has been described which consists of a tubular element, of general cylindrical shape, whose wall comprises a relatively smooth and soft biocompatible material, for example a silicone rubber, at least in its outer part. This tubular element is sufficiently flexible to conform to the anatomical profile of the urethra and to its movements, but sufficiently rigid, particularly in the radial or diametral direction, to maintain an artificial passage in the urethra. This tubular element is intended to be placed in the urethra, without passing through the striated muscular sphincter, in the prostatic segment and/or in any one of the membranous, bulbar, perineal, and penile segments.
  • [0006]
    “Tubular element” is understood to mean any element whose outer surface is described by a generatrix corresponding to a straight or curved line, or other line, about an axis.
  • [0007]
    According to the document FR-A-2 667 783, the tubular element is supported in the urethra principally by the elastic bearing of the wall of said element, in radial extension, against the urethral wall, and secondarily by various notches formed in the wall of the same tubular element, freeing catches which fasten on the urethral wall, somewhat in the manner of scales.
  • [0008]
    In practice, such a prosthesis is not self-stabilizing, for various reasons:
  • [0009]
    the elastic bearing of the tubular element is insufficient to support it in position in the urethra, except by providing or obtaining a very substantial bearing which is likely to damage the urethral wall, leading to the patient experiencing pain, and in any case rendering the withdrawal of the implanted prosthesis difficult or impossible,
  • [0010]
    the fastening catches, or scales, cooperate with the urethral wall, in its longitudinal direction, only in the sense of precluding or limiting the descent of the prosthesis; these fastening catches cannot therefore prevent the prosthesis from ascending,
  • [0011]
    the externally smooth nature of the tubular element encourages its natural sliding against the urethral wall, in particular during the various movements of the urethra,
  • [0012]
    and, finally, the various notches constitute as many punctiform bearing surfaces, or zones of turbulence, on which both the static pressure and the dynamic pressure of the urinary flow act during miction; this has the result of encouraging the descent of the urethral prosthesis.
  • [0013]
    In accordance with the document WO91/16005, metal prostheses are furthermore known which consist of two metal elements, each consisting of metal coils, either contiguous or non-contiguous, which are intended to be arranged in the urethra on either side, respectively, of the striated muscular sphincter. For each element, these coils, which are compressible in a centripetal manner and are expansible in a centrifugal manner, define, in their expanded position, an enveloping surface with a cross section varying from one end to the other.
  • [0014]
    Prostheses are also known which consist of a metallic or non-metallic tube which is perforated and is expansible at the moment of its implantation in the urethra.
  • [0015]
    At present, the various urethral prostheses proposed and described have been unable to reconcile:
  • [0016]
    on the one hand, self-stabilization, which presupposes in one way or another, in the previous solutions, a certain anchoring of the prosthesis on the mucosa of the urethral wall,
  • [0017]
    and, on the other hand, ease of introduction and especially of withdrawal of the prosthesis, that is to say its reversibility.
  • SUMMARY
  • [0018]
    The present invention relates to a prosthesis, and in particular an endo-urethral prosthesis, which is self-stabilizing and which can be introduced and withdrawn in a non-traumatic manner from the natural lumen or tract in which it is implanted.
  • [0019]
    A prosthesis according to the invention comprises two tubular elements which are made from a relatively smooth and soft biocompatible material, such as a silicone rubber, and which are intended to be arranged in the lumen on either side, respectively, of the sphincter, and to be attached to each other by a flexible and deformable connection means which is intended to be held in the orifice of the sphincter. Each element has an external cross section which is substantially constant from one end to the other of said element.
  • [0020]
    The connection means preferably consists of a flexible sleeve, the two ends of which are connected, in continuity of flow, to the two tubular elements respectively; this connection means can also be a single connecting thread or several connecting threads which are attached individually at their two ends to the two tubular elements, respectively.
  • [0021]
    A prosthesis which comprises the technical characteristics defined hereinabove moreover affords the following decisive advantages.
  • [0022]
    The “flexible sleeve or connection means constitutes a predetermined zone of bending of the prosthesis, which is capable of absorbing without stiffness all the movements of the natural lumen. This predetermined zone of bending permits harmonious functioning of the sphincter. The length of this flexible sleeve is moreover adapted to that of the sphincter.
  • [0023]
    Such a prosthesis has a uniform external profile, which fact renders it non-traumatic, both during its insertion and its removal, which maneuvers can be carried out without general anesthesia, and which fact makes it easy to position. This also makes it biocompatible in the sense that it does not irritate the inner mucosa of the natural lumen or tract.
  • [0024]
    Such a prosthesis also has an inner surface which is continuous and uniform, in particular as regards its internal cross section, which fact confers upon it very good hydraulic properties, that is to say without obstacle, for example, vis-á-vis urinary flow. As far as miction is concerned, a urethral prosthesis according to the invention is not moved by the urinary flow.
  • [0025]
    Such a prosthesis is self-stabilizing with respect to the sphincter: at rest, the sphincter immobilizes it, and during miction its sliding is prevented by the two tubular elements which are in abutment, respectively, on either side of the sphincter.
  • [0026]
    Such a prosthesis is also particularly easy to put into place, using simple instruments, in particular without necessarily having recourse to endoscopic or radiological checks. In particular, as is explained hereinafter, by simply sliding the endo-urethral prosthesis along the urethra, it is immobilized automatically in the correct position at the moment when the flexible sleeve arrives at the level of the sphincter which closes over it.
  • [0027]
    Essentially, such a prosthesis does not impede or disturb the functions of the sphincter; it opens and closes, and thus functions in a symmetrical and fluid-tight manner, under the action of the sphincter.
  • BRIEF DESCRIPTION OF THE DRAWINGS
  • [0028]
    The present invention is now described with reference to the attached drawings, in which:
  • [0029]
    FIG. 1 represents an endo-urethral prosthesis in accordance with a first embodiment of the invention;
  • [0030]
    FIG. 2 represents an anatomical section of the urinary tract of the human male; a prosthesis according to FIG. 1 is represented in this section, in its implanted position;
  • [0031]
    FIGS. 3 and 4 are diagrammatic representations showing the cooperation of a prosthesis according to the invention and the striated muscular sphincter; FIG. 3 shows the prosthesis in the flow position with the sphincter relaxed; FIG. 4 shows the prosthesis in the closed position with the sphincter contracted;
  • [0032]
    FIG. 5 represents three variants, designated (a) through (c), of a flexible sleeve belonging to a prosthesis according to FIG. 1; each variant (a) through (c) is represented respectively in the flow position (miction) and in the closed position (continence) and in cross section;
  • [0033]
    FIG. 6 represents an endo-urethral prosthesis in accordance with a second embodiment of the invention;
  • [0034]
    FIG. 7 represents an endo-urethral prosthesis in accordance with a third embodiment of the invention;
  • [0035]
    FIG. 8 represents an assembly for insertion of a prosthesis according to FIG. 6, this assembly being shown at the top in FIG. 8 b in the position in which it is detached from the prosthesis, and at the bottom in FIG. 8 a in the position in which it is engaged on the prosthesis;
  • [0036]
    FIGS. 9 through 12 represent, respectively, four successive stages of the procedure for insertion of a prosthesis according to FIG. 6; and
  • [0037]
    FIG. 13 represents a prosthesis in accordance with an embodiment of the invention;
  • [0038]
    FIG. 14 illustrates an exemplary embodiment of a prosthetic stent according to this invention, in which the flexible connecting element is a thread; and
  • [0039]
    FIG. 15 illustrates an exemplary embodiment of a prosthetic stent according to this invention, in which the flexible connecting element is a plurality of threads.
  • DETAILED DESCRIPTION OF EMBODIMENTS
  • [0040]
    In accordance with FIG. 2, the urethra 1 extends upwards from the meatus urinarius 7 as far as the neck 3 of the bladder 2. Above the striated muscular sphincter 5, the urethra comprises a super-collicular prostatic segment 101 and a sub-collicular prostatic segment 102 on either side of the verumontanum. Below the sphincter 5, the urethra comprises, toward the meatus 7, the membranous segment 103, the bulbar segment 104, the perineal segment 105, and, finally, the penile segment 106.
  • [0041]
    A prosthesis 8 according to the invention, such as is represented in FIG. 1, is intended to be implanted, as will be described hereinafter, in the urethra 1 on either side of the sphincter 5.
  • [0042]
    Ex vivo, that is to say in its non-implanted state, as represented in FIG. 1, a prosthesis 8 according to the invention comprises two tubular elements 9 and 11, of cylindrical shape in the representation in FIG. 1, the wall of which consists of a relatively smooth and soft biocompatible and optionally biodegradable material, for example a silicone rubber. Each tubular element 9 or 11 is sufficiently flexible to conform to the segment of the urethra in which it is to be placed, while at the same time being sufficiently rigid to maintain an artificial endo-urethral passage. Each tubular element 9 or 11 has an external cross section which is substantially constant from one end to the other of said element. These two tubular elements are connected or attached to each other by a connection means which consists, according to the embodiments in FIGS. 1, 6, 7, and 13, of a flexible sleeve 10 which is intended to be held in the orifice of the sphincter 5, as shown, once implanted, in FIG. 2.
  • [0043]
    As is represented in FIG. 2, once put into place, as is described hereinafter, the prosthesis thus comprises, in a continuous manner, the two tubular elements 9 and 11 which are arranged in the urethra 1 on either side, respectively, of the sphincter 5 and are attached to each other via the flexible sleeve 10 which is held in the orifice of the sphincter 5.
  • [0044]
    As is shown in FIG. 1, the two ends of the flexible sleeve 10 are connected, in continuity of flow, to the two tubular elements 9 and 11, respectively. The wall of the sleeve 10 is more flexible, and in particular thinner, than the wall of each tubular element 9 or 11. In practice, this wall of the sleeve 10 can be made from a web of silicone, the tubular elements 9 and 11 for their part consisting of a wall of silicone rubber which is thicker by comparison. The join between the sleeve 10 on the one hand and the two tubular elements 9 and 11 is obtained in any suitable manner, for example by adhesive bonding. As is represented in FIG. 5, the flexible sleeve 10 can be perforated about its circumference, in particular by longitudinal slots or windows, in such a way as to facilitate the bending of the sleeve 10 and to ensure continence; the dimensions of these windows or slots are such that the join between the tubular elements 9 and 11 is reduced to a bundle of strips or threads forming a continuation of said tubular elements 9 and 11.
  • [0045]
    As is shown diagrammatically in FIGS. 3 and 4, the wall of the flexible sleeve 10 is capable of assuming two configurations under the action of the striated muscular sphincter 5, namely a flow configuration represented in FIG. 3, having the shape of a cylinder, upon relaxation of the sphincter 5, and a closed configuration, represented in FIG. 4, corresponding to a biconical or hourglass shape, upon contraction of the sphincter 5.
  • [0046]
    As is represented in FIG. 3, but also in its ex vivo configuration, the tubular elements 9 and 11 form, together with the flexible sleeve 10, a conduit having an internal cross section which is substantially constant in the longitudinal direction of the prosthesis 8. Each tubular element 9 or 11 has an external profile which is substantially constant or uniform in the same longitudinal direction. Irrespective of the configuration, the two ends of the flexible sleeve 10 are connected in flow continuity to the two tubular elements 9 and 11, respectively. This being the case, it is possible, in a manner not shown, and when the caliber of the urethral meatus allows it, for the lower tubular element 11 to have an external cross section greater than that of the upper tubular element 9, for the purpose of promoting self-stabilizing and of preventing upward migration of the prosthesis.
  • [0047]
    As is represented in FIG. 1, ex vivo, that is to say free of any stress imposed by its implantation in the urethra, each tubular element 9 or 11 can have a predetermined and adapted angulation, along its axis, identical to or different than the natural or physiological angulation of the segment in which said tubular element is intended to be implanted. More specifically, taking into consideration the direction and orientation of implantation according to FIG. 2, the upper tubular segment 9 can have an angulation of between 140 and 160°, and preferably one equal to 150°, and the lower tubular segment 11 can have an angulation of between 110 and 130°, and preferably one equal to 120°. This angulation is remanent, which means that under stress it can be suppressed, but that, when there is no stress, each tubular element essentially recovers, in an elastic manner, its original angulation. The angulation used, for example that of the lower tubular element 11 in its part adjacent to the sleeve 10 facing the sphincter 5, can be chosen to contrast with the anatomical shape of the urethra, for example of the bulbar segment 104, and thus to counter the upward migration of the prosthesis through the sphincter 5.
  • [0048]
    The external diameter of the two tubular elements is about 7.3 mm (22 in accordance with the Charriére scale); it can be 8 mm (Charriére 24) for the lower tubular element.
  • [0049]
    As is shown in FIG. 1, the prosthesis 8 comprises a removal thread 14 at its lower end 15, still in the direction of implantation represented in FIG. 2.
  • [0050]
    In accordance with the embodiment represented in FIG. 13, each tubular element 9 or 11 can be perforated, with perforations 51 distributed along its length at the side near its free end, that is to say opposite the sleeve 10; these perforations promote the embedding of the prosthesis with respect to the urethral wall.
  • [0051]
    In accordance with the embodiment represented in FIG. 7, the upper tubular element 9 has one or more notches distributed along its length, for example a helical notch 9 a, in the manner of a screw thread, or notches in a staggered arrangement, and this is again to promote the elimination of the natural secretions of the prostate or tissue debris freed by treatment thereof.
  • [0052]
    As is shown in FIG. 13, a metallic or non-metallic coil 52 constitutes a reinforcement for each tubular element 9 or 11. It is embedded in the elastomeric material of the tube of each tubular element, as is represented in FIG. 13, but it can also be externally exposed, for example for the purpose of therapeutic treatment of the urethral wall. The reinforcement 52 of each tubular element 9 or 11 extends from the sleeve 10 over only a part of the length of said tubular element, in such a way that the remaining part can be cut, for example in order to adapt the length of the tubular element 9 to that of the prostatic segment 101/102, or to adapt the length of the tubular element 11 with respect to the site of a stenosis in that portion of the urethra 1 below the sphincter 5.
  • [0053]
    As is shown in FIG. 13, the elastomeric material covers the metallic reinforcement 52, at least toward the outside, and thus constitutes at least the external part of each tubular element 9 or 11 in contact with the urethral wall.
  • [0054]
    In accordance with FIGS. 6 and 7, the upper end of the upper tubular element 9, that is to say the end opposite the connection sleeve 10, is closed transversely and is presented in the form of a convex and rounded stump 9 b. This stump has one or two lateral orifices 9 c for communicating with the inside of the tubular element 9.
  • [0055]
    Each tubular element 9 or 11 can be coated on its outer surface with a therapeutic substance for the purpose of treating the urethra.
  • [0056]
    In accordance with FIG. 8 b, in order to insert a urethral prosthesis in accordance with FIG. 6 or FIG. 7, an assembly is used which comprises:
  • [0057]
    a semi-rigid and hollow mandrel 60 whose external cross section is adapted to receive the prosthesis 8 which is engaged onto it; this mandrel has, at one extremity, a conical outer limit stop 61, and, at the other extremity, a sealed end 62 against which the closed end 9 b of the prosthesis 8 comes into abutment in its engaged position; this sealed end 62 of the mandrel 60 has an eyelet 62 a for flow inside the mandrel 60, which eyelet 62 a can be brought into line with the lateral orifice 9 c of the prosthesis, again in its engaged position;
  • [0058]
    a rigid and hollow pusher 63 whose internal cross section is adapted for engagement of said pusher on the semi-rigid mandrel 60; the length of the pusher 63 is adapted to act, in its engaged position, as a spacer between the engaged prosthesis 8 and the outer limit stop 61 of the mandrel 60.
  • [0059]
    The insertion device previously described is used in the following manner.
  • [0060]
    A single component is formed from:
  • [0061]
    the mandrel 60;
  • [0062]
    the pusher 63, engaged on the mandrel 60, and coming into abutment against its proximal end, formed by the conical limit stop 61;
  • [0063]
    and, finally, the prosthesis 8 which is also engaged on the free end of the mandrel 60 so as to come into abutment via its end 9 b against the free end 62 of the mandrel 60.
  • [0064]
    In this assembled position, represented at the bottom in FIG. 8 a, the pusher 63 acts as a spacer between the prosthesis 8 and the outer limit stop 61 of the mandrel 60. The prosthesis 8 is oriented angularly with respect to the mandrel 60, in such a way that the flow eyelet 62 a is in line with the lateral orifice 9 c of the prosthesis, of greater cross section.
  • [0065]
    Following lubrication of the duct 1 of the urethra, the assembly which has been formed is inserted through the urethral meatus 7 until the upper end 9 b of the prosthesis opens into the bladder 2. From this moment, the flow of urine through the mandrel 60 indicates that the insertion device has arrived in the bladder, in accordance with the position represented in FIG. 9.
  • [0066]
    The mandrel 60 is then released and withdrawn, while at the same time keeping the pusher 63 in position in the urethra in such a way that the prosthesis 8 does not move; compare FIG. 10.
  • [0067]
    Once the mandrel 60 has been withdrawn, the pusher 63 is itself withdrawn from the urethra 1; compare FIG. 11. At this stage, the lower tubular element 11 of the prosthesis 8 is situated level with the striated muscular sphincter.
  • [0068]
    A gentle downward pull, exerted via the thread 14, makes it possible to slide the lower tubular element 11 and to engage the flexible sleeve 10 in the sphincter.
  • [0069]
    At this moment, the operating surgeon immediately experiences a blocking effect on withdrawal, which corresponds to the correct positioning of the prosthesis 8 with respect to the sphincter 5 which closes on the flexible sleeve 10. The correct position of the prosthesis is thus found automatically; compare FIG. 12.
  • [0070]
    During this last operation, the operating surgeon can also use his/her index finger to perform rectal touch exploration since the lower tubular element 11 is clearly felt by the finger, and its passage this side of the sphincter 5 is clearly noted, with the disappearance of the firmness of said lower tubular element, replaced by the flexible sleeve 10. The correct positioning of the prosthesis 8 with respect to the sphincter 5 is completely painless, and it does not necessitate the use of any rigid instruments, for example forceps. Nor does it necessitate any radiological checks. At the very most, it may be facilitated by the use of an echography probe, which replaces the finger in the rectum.
  • [0071]
    From FIG. 12, the prosthesis in place can be easily withdrawn, using forceps for example, by simply pulling on the free edge of the lower tubular element 11; the resistance of the sphincter 5 is low since the closure pressure of the latter is less than the pressure exerted by a 100 cm water column. As the upper element 9 is engaged in the sphincter 5, the sliding and withdrawal of the prosthesis 8 are effected without them catching at all on the urethral wall.
  • [0072]
    A prosthesis in accordance with FIG. 6, put into place with an insertion device according to FIG. 8, is at one and the same time non-traumatic, positioned in a quasi-automatic manner with respect to the sphincter, and self-stabilizing.
  • [0073]
    This prosthesis is non-traumatic both by virtue of its external configuration and by virtue of its handling:
  • [0074]
    its configuration is non-traumatic on account of its convex or rounded, and optionally flexible, upper end 9 b, which prevents any traumatism of the urethral mucosa, and thus any bleeding, on account of its virtually smooth external surface, that is to say without any specific roughening or reliefs, and on account of the flexible intermediate sleeve, permitting the normal action of the sphincter;
  • [0075]
    its handling is non-traumatic since, as has been described above, its positioning is as gentle and straightforward as that of an indwelling catheter; by permitting the normal functioning of the sphincter, the prosthesis is presented in the manner of an indwelling continence catheter; throughout the period during which the patient is provided with this prosthesis, the bladder is not injured, which fact prevents any formation of clots; and at the moment of its withdrawal, the prosthesis 8 slides out as a single piece without causing the patient any particular pain.
  • [0076]
    The positioning of a prosthesis according to the invention is quasi automatic since in the final analysis it is effected by means of simple tactile perception of a resistance at the moment when the sphincter closes on the flexible sleeve 10. According to the invention, the positioning is based on tactile locating, both by the traction exerted on the thread 14, and/or by a rectal touch exploration by which it is possible to detect the completion of the passage of the lower tubular element 11 through the sphincter 5. And, according to the invention, any error in positioning can be rectified by moving the prosthesis by means of a slight traction which causes the patient little pain and which for this reason does not necessitate general anesthesia.
  • [0077]
    And, the prosthesis is self-stabilizing by virtue of the presence of the two tubular elements 9 and 11 on either side of the sphincter 5. This self-stabilizing can furthermore be improved by the presence of orifices or notches, as described in FIGS. 7 and 13, in which the urethral mucosa engages.
  • [0078]
    FIG. 14 illustrates an exemplary embodiment of a prosthesis intended to be implanted in the urethra on either side of the sphincter. Ex vivo, that is to say in its non-implanted state, the prosthesis comprises two elements 2 and 3. These two elements are connected or attached to each other by a thread 30, which is intended to be held in the orifice
  • [0079]
    FIG. 15 illustrates an exemplary embodiment of a prosthesis intended to be implanted in the urethra on either side of the sphincter. As with the prosthesis of FIG. 14, the prosthesis of FIG. 15 comprises two elements 2 and 3. However, in this embodiment, these two elements are connected or attached by a plurality of threads 30.

Claims (22)

  1. 1. A prosthesis capable of being inserted in a biological lumen or tract, comprising:
    first and second elements that are locatable on respective distal and proximal sides of a sphincter surrounding the lumen or tract, wherein the first element is sufficiently flexible to at least partially conform to the lumen or tract and sufficiently rigid to maintain a passage through the lumen or tract, and wherein the second element comprises a surface that abuts the proximal side of the sphincter; and
    a connecting element interconnecting the first element and the second element, wherein the connecting element comprises a middle portion locatable in the sphincter that is deformable in response to pressure by the sphincter to allow the sphincter to close naturally and thereby close the lumen or tract to natural fluid flows.
  2. 2. The prosthesis of claim 1, wherein the lumen or tract is the human male urethra.
  3. 3. The prosthesis of claim 2, wherein the first element is tubular and traverses at least a portion of a segment of the male urethra extending between the bladder and the distal side of the sphincter.
  4. 4. The prosthesis of claim 3, wherein the tubular element comprises a distal end and proximal end, and the distal end resides at least partially within the bladder when placed in the male urethra.
  5. 5. The prosthesis of claim 4, wherein a tip of the distal end of the tubular element is closed and has a convex shape.
  6. 6. The prosthesis of claim 5, wherein the proximal end of the tubular element comprises a proximal end opening, the distal end of the tubular element along a surface residing within the bladder comprises a side opening, and a lumen extends within the tubular element providing fluid communication between the proximal end opening and the side opening.
  7. 7. The prosthesis of claim 1, wherein one or both of the first and second elements comprises silicone rubber.
  8. 8. The prosthesis of claim 1, wherein the second element comprises a cross-sectional diameter along at least a portion of the second element that is larger than a cross-sectional diameter along at least a portion of the first element.
  9. 9. The prosthesis of claim 4, wherein the second element comprises a cross-sectional diameter along at least a portion of the second element that is larger than a cross-sectional diameter along at least a portion of the tubular element.
  10. 10. The prosthesis of claim 9, wherein the second element comprises an angulated exterior surface that extends along a longitudinal axis of the lumen.
  11. 11. The prosthesis of claim 3, wherein the abutting surface counters upward migration of the tubular segment further into the bladder once the prosthesis is deployed.
  12. 12. The prosthesis of claim 3, wherein the second element is locatable within a bulbar urethral segment extending from the proximal side of the sphincter.
  13. 13. The prosthesis of claim 12, wherein the second element comprises a surface that conforms to a surface of the bulbar urethral segment.
  14. 14. A method of treating an obstruction of a male urethra, comprising:
    supporting said male urethra at a site of said obstruction with the prosthesis of claim 1 by inserting said prosthesis into said male urethra so that said first element supports said male urethra at said site of said obstruction.
  15. 15. A prosthesis capable of being inserted in a biological lumen or tract, comprising:
    first and second elements that are locatable on either side of a sphincter surrounding the lumen or tract, wherein at least one of said first and second elements is sufficiently flexible to conform to the lumen or tract and sufficiently rigid to maintain a passage through the lumen or tract against a force that tends to obstruct the lumen or tract; and
    a connecting element comprising at least one thread, wherein the thread traverses the sphincter and interconnects the first and second elements.
  16. 16. The prosthesis of claim 15, wherein abutment of the second element against the sphincter can inhibit upward migration of the first element.
  17. 17. The prosthesis of claim 15, wherein said connecting element comprises a plurality of threads.
  18. 18. A method of treating an obstruction of a male urethra, comprising:
    supporting said male urethra at a site of said obstruction with the prosthesis of claim 15 by inserting said prosthesis into said male urethra so that said first element supports said male urethra at said site of said obstruction.
  19. 19. A prosthesis for implanting in a lumen, comprising a first tubular element, a second element, and a connecting element, said connecting element comprising a plurality of threads, wherein the first and second elements are locatable on either side of a sphincter surrounding the lumen and the plurality of threads traverse the sphincter and interconnect said first and second elements.
  20. 20. A method of treating an obstruction of a male urethra, comprising:
    supporting said male urethra at a site of said obstruction with the prosthesis of claim 19 by inserting said prosthesis into said male urethra so that said first element supports said male urethra at said site of said obstruction.
  21. 21. An intraurethral device, comprising:
    (i) a first tubular element comprising a flexible, biocompatible material, and comprising a proximal portion and a distal portion, and a central portion with a substantially constant outer diameter, wherein said proximal portion comprises an end opening to allow passage of fluid and said distal portion comprises an opening to allow urine to enter said first tubular element from the bladder;
    (ii) a second element comprising a flexible, biocompatible material, and comprising a proximal end and a distal end, wherein a width dimension along at least a portion of the second element is greater than the outer diameter of the central portion of the first tubular element; and
    (iii) a connecting element comprising at least one thread connecting said proximal portion of said first element to said distal end of said second element.
  22. 22. A method of treating an obstruction of a male urethra, comprising:
    supporting said male urethra at a site of said obstruction with the prosthesis of claim 21 by inserting said prosthesis into said male urethra so that said first element supports said male urethra at said site of said obstruction.
US11338818 1993-02-19 2006-01-25 Prosthesis intended for the treatment of a natural lumen or tract, in particular an endo-urethral prosthesis Abandoned US20060122709A1 (en)

Priority Applications (8)

Application Number Priority Date Filing Date Title
FR9302284A FR2701648B1 (en) 1993-02-19 1993-02-19 A prosthesis for treating a natural lumen or passage, in particular endo-urethral prosthesis.
FR9302284 1993-02-19
US08501140 US5766209A (en) 1993-02-19 1994-02-16 Prosthesis intended for the treatment of a natural lumen or tract, in particular an endo-urethral prosthesis
PCT/FR1994/000171 WO1994018907A1 (en) 1993-02-19 1994-02-16 Prosthesis for treating a natural channel or lumen, particularly an endo-urethral prosthesis
US09032978 US6290666B1 (en) 1993-02-19 1998-03-02 Prosthesis intended for the treatment of a natural lumen or tract, in particular an endo-urethral prosthesis
US09899112 US6576008B2 (en) 1993-02-19 2001-07-06 Methods and device for inserting and withdrawing a two piece stent across a constricting anatomic structure
US10447110 US20030199988A1 (en) 1993-02-19 2003-05-29 Method and device for inserting and withdrawing a two piece stent across a constricting anatomic structure
US11338818 US20060122709A1 (en) 1993-02-19 2006-01-25 Prosthesis intended for the treatment of a natural lumen or tract, in particular an endo-urethral prosthesis

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US11338818 US20060122709A1 (en) 1993-02-19 2006-01-25 Prosthesis intended for the treatment of a natural lumen or tract, in particular an endo-urethral prosthesis

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US11338818 Abandoned US20060122709A1 (en) 1993-02-19 2006-01-25 Prosthesis intended for the treatment of a natural lumen or tract, in particular an endo-urethral prosthesis

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Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20040093065A1 (en) * 2002-11-13 2004-05-13 Allium Inc. Endoluminal lining
US20040127996A1 (en) * 2001-05-15 2004-07-01 Reever Kenneth P. Delivering an agent to a patient's body
US20060189951A1 (en) * 2002-08-21 2006-08-24 Kim Jae H Bowel management system and waste collection bag therefor
US8016816B2 (en) 2003-09-09 2011-09-13 Convatec Technologies Inc. Fecal management appliance and method and apparatus for introducing same

Families Citing this family (24)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20040111108A1 (en) * 2001-11-09 2004-06-10 Farnan Robert C. Balloon catheter with non-deployable stent
CN100502806C (en) * 2001-11-09 2009-06-24 诺沃斯特公司 Balloon catheter with non-deployable stent
US8080026B2 (en) 2003-01-21 2011-12-20 Angioscore, Inc. Apparatus and methods for treating hardened vascular lesions
US7686824B2 (en) 2003-01-21 2010-03-30 Angioscore, Inc. Apparatus and methods for treating hardened vascular lesions
US20050171511A1 (en) * 2003-05-01 2005-08-04 High Kenneth A. Catheter capture device
US20050143690A1 (en) * 2003-05-01 2005-06-30 High Kenneth A. Cystotomy catheter capture device and methods of using same
US7662145B2 (en) * 2003-09-17 2010-02-16 Prostalund Operations Ab Partial-length indwelling urinary catheter and method permitting selective urine discharge
US20060259005A1 (en) 2005-05-11 2006-11-16 Angioscore, Inc. Methods and systems for delivering substances into luminal walls
US20070106375A1 (en) * 2005-11-07 2007-05-10 Carlos Vonderwalde Bifurcated stent assembly
US8292827B2 (en) 2005-12-12 2012-10-23 Boston Scientific Scimed, Inc. Micromachined medical devices
US20070208405A1 (en) * 2006-03-06 2007-09-06 Boston Scientific Scimed, Inc. Stent delivery catheter
US8133265B2 (en) * 2006-06-30 2012-03-13 Olympus Medical Systems Corp. Guide catheter, and stent delivery system
US9339632B2 (en) 2006-09-27 2016-05-17 Boston Scientific Scimed, Inc. Catheter shaft designs
US7981148B2 (en) 2007-05-16 2011-07-19 Boston Scientific Scimed, Inc. Stent delivery catheter
US8118826B2 (en) * 2007-09-27 2012-02-21 Swan Valley Medical, Incorporated Method of performing a suprapubic transurethral cystostomy and associated procedures and apparatus therefor
US8382785B2 (en) * 2007-09-27 2013-02-26 Swan Valley Medical Incorporated Apparatus and method for performing cystotomy procedures
US20090105687A1 (en) * 2007-10-05 2009-04-23 Angioscore, Inc. Scoring catheter with drug delivery membrane
US20090157048A1 (en) * 2007-12-18 2009-06-18 Boston Scientific Scimed, Inc. Spiral cut hypotube
US8460213B2 (en) 2008-01-03 2013-06-11 Boston Scientific Scimed, Inc. Cut tubular members for a medical device and methods for making and using the same
WO2009126244A3 (en) * 2008-04-07 2010-01-21 Bioabsorbable Therapeutics Devices, systems, and methods for joining body conduits
US9956100B2 (en) 2009-09-15 2018-05-01 Brightwater Medical, Inc. Systems and methods for coupling and decoupling a catheter
EP2380604A1 (en) 2010-04-19 2011-10-26 InnoRa Gmbh Improved coating formulations for scoring or cutting balloon catheters
US8632559B2 (en) 2010-09-21 2014-01-21 Angioscore, Inc. Method and system for treating valve stenosis
WO2016004283A1 (en) * 2014-07-02 2016-01-07 The Cleveland Clinic Foundation Anastomosis devices and methods of using same

Citations (22)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3527226A (en) * 1966-02-03 1970-09-08 Cordis Corp Ventricular catheter with valve and pump flushing means
US3657744A (en) * 1970-05-08 1972-04-25 Univ Minnesota Method for fixing prosthetic implants in a living body
US3938529A (en) * 1974-07-22 1976-02-17 Gibbons Robert P Indwelling ureteral catheter
US4240434A (en) * 1978-10-10 1980-12-23 Newkirk John B Peritoneo-venous shunt
US4423725A (en) * 1982-03-31 1984-01-03 Baran Ostap E Multiple surgical cuff
US4432757A (en) * 1980-05-09 1984-02-21 Davis Jr Richard C Indwelling urethral catheter
US4973301A (en) * 1989-07-11 1990-11-27 Israel Nissenkorn Catheter and method of using same
US5059169A (en) * 1989-07-07 1991-10-22 C. R. Bard, Inc. High-friction prostatic stent
US5078720A (en) * 1990-05-02 1992-01-07 American Medical Systems, Inc. Stent placement instrument and method
US5104404A (en) * 1989-10-02 1992-04-14 Medtronic, Inc. Articulated stent
US5122154A (en) * 1990-08-15 1992-06-16 Rhodes Valentine J Endovascular bypass graft
US5176625A (en) * 1990-10-25 1993-01-05 Brisson A Glen Stent for ureter
US5207695A (en) * 1989-06-19 1993-05-04 Trout Iii Hugh H Aortic graft, implantation device, and method for repairing aortic aneurysm
US5269802A (en) * 1991-09-10 1993-12-14 Garber Bruce B Prostatic stent
US5282824A (en) * 1990-10-09 1994-02-01 Cook, Incorporated Percutaneous stent assembly
US5282784A (en) * 1991-10-09 1994-02-01 Mentor Corporation Injection stent system
US5292802A (en) * 1988-11-21 1994-03-08 Collagen Corporation Collagen-polymer tubes for use in vascular surgery
US5322501A (en) * 1992-10-02 1994-06-21 Mahmud Durrani Ayaz Continent urethral stent for treating and preventing urethral stricture after surgery
US5514112A (en) * 1992-10-02 1996-05-07 Boston Scientific Corporation Drainage catheter and method of use
US5736127A (en) * 1992-04-06 1998-04-07 Hymedix International, Inc. Polymeric nitrogen-containing drug salt forms for controlled release
US5792400A (en) * 1988-11-10 1998-08-11 Biocon Oy Method of manufacturing biodegradable surgical implants and devices
US6238368B1 (en) * 1994-07-13 2001-05-29 Marian Devonec Therapeutic device for the selective cytoreduction treatment of an obstruction

Family Cites Families (31)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3257226A (en) * 1962-11-08 1966-06-21 Exxon Research Engineering Co Wax coating method and apparatus
US4350161A (en) 1980-05-09 1982-09-21 Davis Jr Richard C Indwelling urethral catheter and method
EP0556940A1 (en) 1986-02-24 1993-08-25 Robert E. Fischell Intravascular stent
US4895566A (en) 1986-07-25 1990-01-23 C. R. Bard, Inc. Coating medical devices with cationic antibiotics
DK163713C (en) 1987-09-02 1992-09-07 Ole Gyring Nieben Device for planting a partial catheter into a body cavity
US4932958A (en) 1988-05-10 1990-06-12 American Medical Systems, Inc. Prostate balloon dilator
US5098874A (en) * 1988-09-21 1992-03-24 Magnetic Peripherals Inc. Improved ceramic head pad materials
US5116309A (en) * 1989-01-25 1992-05-26 Coll Milton E Ureteral stent-catheter system having varying diameter stent
US4990155A (en) 1989-05-19 1991-02-05 Wilkoff Howard M Surgical stent method and apparatus
US5078725A (en) * 1989-11-09 1992-01-07 C. R. Bard, Inc. Balloon catheter and techniques for dilating obstructed lumens and other luminal procedures
DE69108423T2 (en) 1990-02-08 1995-07-27 Howmedica Inflatable dilator.
EP0525110B1 (en) 1990-04-19 1997-06-04 InStent Inc. Device for the treatment of constricted vessels
US5258020A (en) 1990-09-14 1993-11-02 Michael Froix Method of using expandable polymeric stent with memory
US5222971A (en) 1990-10-09 1993-06-29 Scimed Life Systems, Inc. Temporary stent and methods for use and manufacture
FR2667783B1 (en) 1990-10-11 1995-06-02 Berberian Jean Pierre
US5152749A (en) 1991-06-28 1992-10-06 American Medical Systems, Inc. Instrument placement apparatus
US5176626A (en) 1992-01-15 1993-01-05 Wilson-Cook Medical, Inc. Indwelling stent
US5152249A (en) * 1992-03-16 1992-10-06 Howe Steve R Attachment device for animal ear tag
US5282823A (en) 1992-03-19 1994-02-01 Medtronic, Inc. Intravascular radially expandable stent
US5419760A (en) 1993-01-08 1995-05-30 Pdt Systems, Inc. Medicament dispensing stent for prevention of restenosis of a blood vessel
FR2701648B1 (en) 1993-02-19 1995-03-31 Marian Devonec A prosthesis for treating a natural lumen or passage, in particular endo-urethral prosthesis.
FR2706764B1 (en) 1993-06-24 1995-08-04 Synthelabo
US5499994A (en) * 1993-07-30 1996-03-19 American Medical Systems, Inc. Dilation device for the urethra
US5429634A (en) 1993-09-09 1995-07-04 Pdt Systems Biogenic implant for drug delivery and method
DE29507519U1 (en) * 1995-05-05 1995-08-10 Angiomed Ag Endosphincter and set for releasably sealing the urethra
FR2736554B1 (en) * 1995-07-10 1997-08-29 Devonec Marian Catheter as a means of catheterization and a means of separable introduction, useful for the treatment of prostate obstacles in humans
US5830179A (en) * 1996-04-09 1998-11-03 Endocare, Inc. Urological stent therapy system and method
US5971967A (en) * 1997-08-19 1999-10-26 Abbeymoor Medical, Inc. Urethral device with anchoring system
US6494879B2 (en) * 1998-10-15 2002-12-17 Scimed Life Systems, Inc. Treating urinary retention
US6685745B2 (en) * 2001-05-15 2004-02-03 Scimed Life Systems, Inc. Delivering an agent to a patient's body
US6494855B2 (en) * 2001-05-16 2002-12-17 Scimed Life Systems, Inc. Draining bodily fluid

Patent Citations (22)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3527226A (en) * 1966-02-03 1970-09-08 Cordis Corp Ventricular catheter with valve and pump flushing means
US3657744A (en) * 1970-05-08 1972-04-25 Univ Minnesota Method for fixing prosthetic implants in a living body
US3938529A (en) * 1974-07-22 1976-02-17 Gibbons Robert P Indwelling ureteral catheter
US4240434A (en) * 1978-10-10 1980-12-23 Newkirk John B Peritoneo-venous shunt
US4432757A (en) * 1980-05-09 1984-02-21 Davis Jr Richard C Indwelling urethral catheter
US4423725A (en) * 1982-03-31 1984-01-03 Baran Ostap E Multiple surgical cuff
US5792400A (en) * 1988-11-10 1998-08-11 Biocon Oy Method of manufacturing biodegradable surgical implants and devices
US5292802A (en) * 1988-11-21 1994-03-08 Collagen Corporation Collagen-polymer tubes for use in vascular surgery
US5207695A (en) * 1989-06-19 1993-05-04 Trout Iii Hugh H Aortic graft, implantation device, and method for repairing aortic aneurysm
US5059169A (en) * 1989-07-07 1991-10-22 C. R. Bard, Inc. High-friction prostatic stent
US4973301A (en) * 1989-07-11 1990-11-27 Israel Nissenkorn Catheter and method of using same
US5104404A (en) * 1989-10-02 1992-04-14 Medtronic, Inc. Articulated stent
US5078720A (en) * 1990-05-02 1992-01-07 American Medical Systems, Inc. Stent placement instrument and method
US5122154A (en) * 1990-08-15 1992-06-16 Rhodes Valentine J Endovascular bypass graft
US5282824A (en) * 1990-10-09 1994-02-01 Cook, Incorporated Percutaneous stent assembly
US5176625A (en) * 1990-10-25 1993-01-05 Brisson A Glen Stent for ureter
US5269802A (en) * 1991-09-10 1993-12-14 Garber Bruce B Prostatic stent
US5282784A (en) * 1991-10-09 1994-02-01 Mentor Corporation Injection stent system
US5736127A (en) * 1992-04-06 1998-04-07 Hymedix International, Inc. Polymeric nitrogen-containing drug salt forms for controlled release
US5322501A (en) * 1992-10-02 1994-06-21 Mahmud Durrani Ayaz Continent urethral stent for treating and preventing urethral stricture after surgery
US5514112A (en) * 1992-10-02 1996-05-07 Boston Scientific Corporation Drainage catheter and method of use
US6238368B1 (en) * 1994-07-13 2001-05-29 Marian Devonec Therapeutic device for the selective cytoreduction treatment of an obstruction

Cited By (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20090164025A1 (en) * 2001-05-15 2009-06-25 Boston Scientific Scimed, Inc. Delivering an agent to a patient's body
US20040127996A1 (en) * 2001-05-15 2004-07-01 Reever Kenneth P. Delivering an agent to a patient's body
US8034119B2 (en) 2001-05-15 2011-10-11 Boston Scientific Scimed, Inc. Delivering an agent to a patient's body
US20060189951A1 (en) * 2002-08-21 2006-08-24 Kim Jae H Bowel management system and waste collection bag therefor
US20090030387A1 (en) * 2002-08-21 2009-01-29 Hollister Incorporated Bowel management system and waste collection bag therefor
US20090030386A1 (en) * 2002-08-21 2009-01-29 Hollister Incorporated Bowel management system and waste collection bag therefor
US8323255B2 (en) 2002-08-21 2012-12-04 Hollister Incorporated Bowel management system
US7722583B2 (en) 2002-08-21 2010-05-25 Hollister Incorporated Bowel management system and waste collection bag therefor
US8801683B2 (en) 2002-08-21 2014-08-12 Hollister Incorporated Bowel management system
US20080262447A2 (en) * 2002-08-21 2008-10-23 Hollister Incorporated Bowel management system and waste collection bag therefor
US20040093065A1 (en) * 2002-11-13 2004-05-13 Allium Inc. Endoluminal lining
US8282678B2 (en) 2002-11-13 2012-10-09 Allium Medical Solutions Ltd. Endoluminal lining
US8016816B2 (en) 2003-09-09 2011-09-13 Convatec Technologies Inc. Fecal management appliance and method and apparatus for introducing same
US8827970B2 (en) 2003-09-09 2014-09-09 Convatec Inc. Fecal management appliance and method and apparatus for introducing same

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US20020128705A1 (en) 2002-09-12 application
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