Classifications

• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61F—FILTERS 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
  • A61F2/00—Filters 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
  • A61F2/02—Prostheses implantable into the body
  • A61F2/04—Hollow or tubular parts of organs, e.g. bladders, tracheae, bronchi or bile ducts
  • A61F2/06—Blood vessels
  • A61F2/064—Blood vessels with special features to facilitate anastomotic coupling
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61F—FILTERS 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
  • A61F2/00—Filters 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
  • A61F2/02—Prostheses implantable into the body
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61F—FILTERS 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
  • A61F2/00—Filters 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
  • A61F2/02—Prostheses implantable into the body
  • A61F2/08—Muscles; Tendons; Ligaments
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61F—FILTERS 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
  • A61F2/00—Filters 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
  • A61F2/02—Prostheses implantable into the body
  • A61F2/08—Muscles; Tendons; Ligaments
  • A61F2002/0894—Muscles

Definitions

• the present invention relates to a device for assembling flexible conduits. We will consider here more particularly the case of the assembly of two blood vessels but, in general, each of these vessels may be any type of duct with non-rigid and flexible wall.
• the stump of a blood vessel, vein or artery is a fragile piece of flesh, difficult to handle, and which one conventionally knows how to connect to another vessel only by means of a seam.
• the present invention provides for transforming the end of the stump into an easily manipulated and connectable object by equipping each stump with a tip that can be connected to a complementary tip.
• the present invention provides a connector for connecting vessels, comprising an internal cylinder insertable inside a part of the end of a vessel, and an external cylinder disposed at the external periphery of said end, l 'one of these two cylinders being able to expand / compress after its establishment, where it follows that the vessel is blocked between the two cylinders after their establishment.
• the internal cylinder is capable of expanding after its installation and the external cylinder is non-expandable, this external cylinder being provided with means for fixing to an external cylinder fitted to another vessel.
• the external cylinder consists of two half-cylinders associated with a temporary fixing means.
• the present invention also relates to a device for assembling vessels respectively equipped with a nozzle, in which each of the external cylinders comprises complementary male and female connection means.
• the first vessel is equipped with a male end piece and the second vessel is equipped with a female end piece whose external cylinder has a diameter greater than that of the external cylinder of the first end piece and whose the less the end part is flexible, this end part being surrounded by two removable half-cylinders themselves surrounded by a stent acting in compression.
• the vessel assembly device uses a nozzle in which the internal cylinder penetrates inside two opposite vessels and the external cylinder surrounds the external periphery of the two vessels .
• FIG. 1 represents an end blood vessel equipped with a tip according to an embodiment of the present invention
• FIGS. 2A-2D illustrate a method of positioning the end piece of FIG. 1
• FIGS. 3A and 3B illustrate an example of application of the present invention to an assembly operation of blood vessels
• Figures 4 to 7 illustrate various variants of devices according to the present invention
• Figure 8 illustrates another embodiment of the present invention.
• a “hollow stent” will be called a hollow cylindrical object with solid or perforated walls made of a material capable of having a first dimension in an initial state (first internal and external diameters) and a second dimension in a final state (of second internal and external diameters). It could be a cylinder whose internal and external diameters tend to decrease or increase, or else a cylinder whose internal diameter tends to decrease or else a cylinder whose external diameter tends to increase. In the case of a cylinder whose external diameter tends to increase, the stent is likely to exert a dilation force on the medium disposed at its external periphery. In the second case, the stent is likely to exert a compression force on the medium located at its internal periphery.
• Such stents can use various physical phenomena. They may, for example, be shape memory materials, pneumatic type devices or even devices with osmotic effect. In the latter case, the stent will consist of a double-walled cylinder containing osmotic material so that the pressure between the two walls increases when the stent is immersed in a liquid, one or both walls being capable of deform.
• FIG. 1 is a perspective view of a blood vessel 1 provided with a tip according to the present invention.
• the tip includes a stent 2 disposed inside the vessel and a non-expandable cylinder 3 disposed outside the vessel.
• the stent is such that, once placed inside the vessel, it tends to increase its diameter so that the vessel 1 is wedged between the stent 2 and the cylinder 3.
• the cylinder 3 intended to serve as support will be called hereinafter “anvil”. It is preferably not a cylinder in a rigid material but of a cylinder made of a non-extensible flexible material, for example a biocompatible, metallic, fabric or plastic cylinder.
• FIGS. 2A to 2D illustrate successive steps of fitting the tip of FIG.
• the introducer has the shape of a small diameter cylinder. It can be introduced through a percutaneous opening. We will call “proximal end” the end of the introducer situated outside the patient, and “distal end” the end of the introducer which is inside the operating field.
• the introducer comprises a core 6 and a sheath 7 movable in translation 1 'relative to one another. An element such as a stent 2 can be housed in the distal part of the sheath.
• the operator can control the orientation and position of the distal end. These movements allow the distal end to be introduced over a few millimeters inside the vessel. This operation may require that the stump be held by a clamp (introduced by another percutaneous opening).
• Stent introducers enable this functionality by means of devices located at the proximal end. This phase is delicate, because the stent can slide relative to the stump.
• a partially reversible introducer device will preferably be chosen. Such a device allows the stent to return to its protective sheath, provided that the stent is not completely extended (typically, the stent must be "deployed” over less than a fixed percentage, for example 80%, of its length). It will be noted that the stent used tends to have a diameter greater than that of the vessel (it is thanks to this difference in diameter that the stent can press the wall of the vessel against that of the anvil). However, at this stage (FIG.
• the anvil has not yet been put in place. We would risk injure the vessel if the stent is deployed too much. It will therefore only be deployed with a length which allows it to take a diameter equivalent to that of the artery (this is done under visual control, an endoscope being installed in the operating field). It will be noted that, when the stent is not too deployed, it is possible to subject it to translational movements along the axis of the stump. This is only possible in the direction which would lead to the extraction of the stent, taking into account the conical nature of the stent when its deployment is incomplete. This will facilitate the correct positioning of the stent.
• the cylindrical anvil 3 is introduced from the proximal end. It is a hollow cylinder which can slide to the stump. Pliers allow it to be put in place. We can then finish the delivery of the stent, by maneuvering the proximal end of the introducer. The stent releases all of its centripetal radial compression force, thereby pressing the vessel wall against the anvil ( Figure 2D).
• two stubs 1 and 11 are provided with male and female end pieces comprising stents 2 and 12 and anvils 3 and 13.
• the female anvil 3 preferably has an end portion of narrowed diameter.
• the male anvil 13 has an end portion made of a flexible but not extensible material.
• at least the end part of the anvil 13 is surrounded by two rigid half-cylinders 14a, 14b each of which is equipped at one end with a lug (small grip projection) 15a, 15b, and a stent 16 tending to contract (to decrease its diameter).
• the half-cylinders 14a, 14b are held in place against one another under the effect of the pressure exerted by the stent 16.
• the cylinders 3 and 13 forming an anvil are provided at their ends with male and female devices 18a and 18b for quick connection.
• Such devices such as for example screw threads, or “clipping” devices, are very common for quickly connecting tubes, particularly those which are used in the medical field.
• Figures 5 and 6 illustrate another embodiment of the present invention in which a single stent 22 is inserted in the two ends of two vessels 1 and 11 and the assembly of these two ends is surrounded at its outer periphery by non-expandable cylinder 23.
• Figure 5 shows the device while the stent 22 is in the initial position, before expansion
• Figure 6 shows the device while the stent is in the expanded position.
• the stent is preferably of the pneumatically or osmotic inflation type.
• FIG. 7 represents another variant of the present invention in which a single stent 22 is inserted inside the two ends of the two vessels 1 and 11 assembled and two anvil cylinders. 25 and 26 are arranged at the outer periphery of the ends vessels.
• FIG. 8 shows another embodiment of the present invention in which a first vessel 1 is associated with a male connector while a second vessel 11 is associated with a female connector.
• the male end piece comprises an internal stent 2 and an external cylinder forming an anvil.
• the outer cylinder consists of two half-cylinders 31a and 31b respectively associated with gripping lugs 32a and 32b.
• the half-cylinders 31a and 31b are assembled by any chosen means, for example by a wire or net 33 which holds them in place and allows them to temporarily play an anvil role.
• the female end piece is flared and comprises two external half-cylinders 35a and 35b, respectively associated with gripping lugs 36a and 36b.
• the blood vessel is everted and pressed against the flaring of the tip to which it is temporarily fixed by staples, wires or the like.
• the assembly is surrounded by a cylindrical stent 37 whose internal diameter tends to reduce.
• the assembly of the male and female ends is carried out by inserting the male end into the female end, cutting the wire or net 33, and successively removing the half-cylinders 32a, 32b, then the half-cylinders 36a and 36b after having detached them from the vessel 11. Then, the connection is ensured by the two stents 2 and 37 operating in antagonism, the stent 2 exerting a force of dilation and the stent 37 a force of compression.
• the outer cylinder, forming an anvil is a cylinder split longitudinally, the two parts facing the slot being fixable to each other after installation, for example by a quick coupling.

Landscapes

• Health & Medical Sciences (AREA)
• Vascular Medicine (AREA)
• Life Sciences & Earth Sciences (AREA)
• Veterinary Medicine (AREA)
• Public Health (AREA)
• Oral & Maxillofacial Surgery (AREA)
• Transplantation (AREA)
• Engineering & Computer Science (AREA)
• Biomedical Technology (AREA)
• General Health & Medical Sciences (AREA)
• Heart & Thoracic Surgery (AREA)
• Cardiology (AREA)
• Animal Behavior & Ethology (AREA)
• Rehabilitation Therapy (AREA)
• Orthopedic Medicine & Surgery (AREA)
• Rheumatology (AREA)
• Gastroenterology & Hepatology (AREA)
• Pulmonology (AREA)
• Prostheses (AREA)
• Media Introduction/Drainage Providing Device (AREA)

Applications Claiming Priority (3)

Publications (1)

Family

ID=8865602

Family Applications (2)

Family Applications After (1)

Country Status (7)

Families Citing this family (32)

Citations (1)

Family Cites Families (31)

• 2001
  • 2001-07-17 FR FR0109526A patent/FR2827502B1/fr not_active Expired - Fee Related
• 2002
  • 2002-07-17 EP EP02770034A patent/EP1414372A2/de not_active Withdrawn
  • 2002-07-17 US US10/484,159 patent/US20040249399A1/en not_active Abandoned
  • 2002-07-17 AU AU2002336139A patent/AU2002336139A1/en not_active Abandoned
  • 2002-07-17 EP EP02767579A patent/EP1414371B1/de not_active Expired - Lifetime
  • 2002-07-17 DE DE60236937T patent/DE60236937D1/de not_active Expired - Lifetime
  • 2002-07-17 JP JP2003513452A patent/JP2004534610A/ja active Pending
  • 2002-07-17 WO PCT/FR2002/002555 patent/WO2003007843A2/fr not_active Ceased
  • 2002-07-17 JP JP2003513453A patent/JP4276939B2/ja not_active Expired - Fee Related
  • 2002-07-17 US US10/484,062 patent/US7611887B2/en not_active Expired - Fee Related
  • 2002-07-17 WO PCT/FR2002/002556 patent/WO2003007844A1/fr not_active Ceased

Patent Citations (1)

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