WO2012107079A1 - Système de revêtement endoluminal - Google Patents

Système de revêtement endoluminal Download PDF

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Publication number
WO2012107079A1
WO2012107079A1 PCT/EP2011/051814 EP2011051814W WO2012107079A1 WO 2012107079 A1 WO2012107079 A1 WO 2012107079A1 EP 2011051814 W EP2011051814 W EP 2011051814W WO 2012107079 A1 WO2012107079 A1 WO 2012107079A1
Authority
WO
WIPO (PCT)
Prior art keywords
ring
distal
compression
lining
proximal
Prior art date
Application number
PCT/EP2011/051814
Other languages
English (en)
Inventor
Alessandro Pastorelli
Jason Harris
Mark Steven Ortiz
Michele D'arcangelo
Original Assignee
Ethicon Endo-Surgery, Inc.
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Ethicon Endo-Surgery, Inc. filed Critical Ethicon Endo-Surgery, Inc.
Priority to PCT/EP2011/051814 priority Critical patent/WO2012107079A1/fr
Publication of WO2012107079A1 publication Critical patent/WO2012107079A1/fr

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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
    • A61F5/00—Orthopaedic methods or devices for non-surgical treatment of bones or joints; Nursing devices; Anti-rape devices
    • A61F5/0003—Apparatus for the treatment of obesity; Anti-eating devices
    • A61F5/0013—Implantable devices or invasive measures
    • A61F5/0076—Implantable devices or invasive measures preventing normal digestion, e.g. Bariatric or gastric sleeves
    • 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
    • A61F5/00—Orthopaedic methods or devices for non-surgical treatment of bones or joints; Nursing devices; Anti-rape devices
    • A61F5/0003—Apparatus for the treatment of obesity; Anti-eating devices
    • A61F5/0089—Instruments for placement or removal

Definitions

  • the present invention relates generally to medical apparatuses and methods and more particularly to devices and methods for positioning and anchoring a lining to a hollow body organ, such as a stomach, intestine or gastrointestinal tract.
  • VBG vertical banded gastroplasty
  • Roux-En-Y gastric bypass a more invasive surgical procedure known as a Roux-En-Y gastric bypass to effect permanent surgical reduction of the stomach's volume and subsequent bypass of the intestine.
  • endoluminal sleeves are known for partially or totally lining certain portions of the stomach and of the intestine with the aim to separate or bypass at least part of the food flow from the lined portions of the gastrointestinal tract. It has been observed that by creating a physical barrier between the ingested food and certain regions of the gastrointestinal wall by means of endoluminal sleeves, similar benefits for weight loss and improvement or resolution of type 2 diabetes may be achieved as with gastric bypass surgery. Physicians believe that by creating a physical barrier between the ingested food and selected regions of the gastrointestinal wall, it might be possible to purposefully influence the mechanism of hormonal signal activation originating from the intestine.
  • a known type of endoluminal sleeve relies on metallic expandable structures, such as a stent, to engage the surrounding hollow organ for holding the sleeve in the planned position.
  • metallic expandable structures such as a stent
  • barbs which penetrate the surrounding tissue.
  • the present invention provides for an improved endoluminal lining system and method for the transoral, or endoscopic, positioning and anchoring of an endoluminal lining within a hollow body organ, particularly the gastrointestinal tract, including, but not limited to, the esophagus, stomach, portions of or the entire length of the intestinal tract, etc., unless specified otherwise.
  • the surgeon or endoscopist may insert devices as described below through the patient's mouth, down the esophagus and into the stomach or intestine as appropriate. The procedure can be performed entirely from within the patient's stomach or other intestinal tract, and does not necessarily require any external incision.
  • an endoluminal lining system for internally lining a hollow organ, particularly a section of the gastrointestinal tract, the system comprising a flexible tubular lining extending between a proximal end and a distal end and an anchoring device for fastening the flexible tubular lining in the hollow organ, the anchoring device comprising a distal compression ring connected to the lining and a proximal compression ring initially separate from the distal compression ring, wherein the distal and proximal compression rings form co-operating opposite tissue clamping surfaces adapted to clamp a ring shaped tissue portion of the hollow organ therebetween and locking means adapted to lock the distal compression ring to the proximal compression ring in a tissue clamping configuration.
  • the lining system comprises flexible guide means, such as a guide wire, which can be fastened to the distal compression ring in a pull resistant manner and slidably received by the proximal compression ring, thereby allowing the distal ring to be pulled towards and coupled with the proximal compression ring.
  • the distal compression ring comprises a support frame forming a guide seat for a pull resistant connection with a guide wire, wherein the guide seat is arranged radially inside the distal compression ring at a distance from the tissue clamping surfaces.
  • the ring locking means comprise at least one pair of diametrically opposite locking pins protruding from one of the distal and proximal compression rings towards the other compression ring and adapted to be received by corresponding locking seats formed in the other compression ring, e.g. by snap fit, shape connection or interference fit. Both the locking seats and the locking pins form a guide channel adapted to receive a guide wire which allows the compression rings to be pulled towards each other and in engagement in a tissue clamping configuration.
  • the locking pins and the locking seats are formed in the tissue clamping surfaces of the distal and proximal compression rings, respectively, and the locking pins are intended to puncture and retain the clamped tissue portion between the compression rings.
  • the anchoring device and, hence, the endoluminal lining can be positioned very precisely by pulling or sliding the compression ring with the locking pins along the predefined guide wire path through the hollow organ wall.
  • the endoluminal lining system comprises a plurality of needles connected to one of the distal and proximal compression rings and movable from a rest position in which pointed free ends of the needles are received inside the compression ring and an activated position in which the pointed free ends of the needles protrude radially outward of the compression ring and are inclined towards the other compression ring.
  • the needles In the activated position, the needles can pierce and retain the organ wall adjacent the compression ring and , during movement of the compression ring towards the other compression ring, the pierced and retained organ wall is pushed together and folded over the clamping surface.
  • the tissue acquisition means may also be separate from the anchoring device and comprise e.g. a plurality of anchoring hooks, e.g. so called T-tags, adapted to be fastened to the organ wall at the anchoring site and flexible pull strings connected to each one of the anchoring hooks and extended through a central passage opening of the proximal compression ring, thereby allowing the fastened organ wall to be pulled between the tissue clamping surfaces from inside the central passage opening.
  • anchoring hooks e.g. so called T-tags
  • At least one of the distal and proximal compression ring is time-dependently bio-fragmentable or absorbable. This makes the endoluminal lining a temporary and reversible therapeutic treatment.
  • the lining system comprises an endoluminal applier for endoluminally delivering and fastening the anchoring device of the lining system to the hollow organ, the applier comprising a ring fastening assembly with a proximal ring holder adapted to hold the proximal compression ring, and a distal ring holder adapted to hold the distal compression ring.
  • the distal ring holder is translatable relative to proximal ring holder and adapted to cooperate with the proximal ring holder for approximating the proximal and distal compression rings and pressing them together.
  • the ring fastening assembly forms a central channel extending longitudinally through the proximal ring holder and through the distal ring holder and, preferably, opening laterally into the space between the proximal and distal ring holders, the central channel being adapted for the passage of an endoscope to visualize both the space between the proximal and distal rings received by the corresponding ring holders and the space distally ahead of the ring fastening assembly and, possibly, to slide the applier endoluminally along the endoscope to a target site in the hollow organ.
  • the applier assures a correct relative positioning of the compression rings during fastening of the anchoring device and allows an improved guidance through the Gl tract and continuous visualization by the endoscope received in the central channel, both during endoluminal insertion and withdrawal of the applier and during fastening of the compression rings.
  • FIG. 1 illustrates an endoluminal lining system with an anchoring device in a disengaged configuration according to an embodiment of the invention
  • FIG. 2 illustrates an insertion step for endoluminally placing a tubular lining in a portion of a Gl tract, using a lining system according to an embodiment
  • FIG. 3 illustrates a tissue fastening step for endoluminally placing a tubular lining in a portion of a Gl tract, using a lining system according to an embodiment
  • FIG. 4 illustrates a target portion of intestine after completion of the tissue fastening step in figure 3;
  • FIG. 5 illustrates a further step of a method for endoluminally placing a tubular lining in a portion of the Gl tract, using a lining system according to an embodiment
  • FIG. 6 illustrates the target portion of intestine and the tubular lining after completion of the endoluminal placement and anchoring procedure
  • Figu re 7 illustrates an endolu minal lining system with an anchoring device in a disengaged configuration in accordance with a further embodiment of the invention
  • FIG. 8 illustrates a tissue fastening and acquisition step of a method for endoluminally placing a tubular lining in a portion of the Gl tract, using a lining system according to an embodiment
  • FIG. 9 is an enlarged view of a detail in figure 8.
  • FIG. 10 illustrates guide wire material inserted in a target portion of a hollow organ wall along a predetermined path for a subsequent tissue acquisition and anchoring of a tubular lining
  • FIGS. 1 1 through 13 illustrate further steps of a method for endoluminally anchoring a tubular lining in a portion of the Gl tract, using the lining system in Figure 7;
  • FIG. 14 illustrates a distal compression ring with an attached tubular lining of an endoluminal lining system in accordance with a further embodiment of the invention
  • FIG. 15 illustrates a tissue acquisition step of a method for endoluminally anchoring a tubular lining in a portion of the Gl tract, using the lining system in figure 14;
  • FIG. 16 illustrates a tissue fastening and clamping step of a method for endoluminally anchoring a tubular lining in a portion of the Gl tract, using the lining system in figure 14;
  • FIG. 17 and 18 illustrate different possible positions of the tubular lining within the Gl tract of a patient
  • FIG. 19 illustrates an applier of the endoluminal lining system in accordance with an embodiment.
  • FIG. 1 depicts an endoluminal lining system for internally lining a hollow organ 1 , particularly a section of the gastrointestinal tract.
  • the system comprises a flexible tubular lining 2 extending between a proximal end 3 and a distal end 4 and an anchoring device 5 for fastening the flexible tubular lining 2 in the hollow organ 1 .
  • the anchoring device 5 comprises a distal compression ring 6 connected to the lining 2 and a proximal compression ring 7 initially separate from the distal compression ring 6.
  • the distal and proximal compression rings 6, 7 form both a central passage opening 1 1 and co-operating opposite tissue clamping surfaces 8, 9 adapted to clamp a ring shaped tissue portion 10 of the hollow organ 1 therebetween, as well as locking means adapted to lock the distal compression ring 6 to the proximal compression ring 7 in a tissue clamping configuration.
  • the lining system comprises flexible guide and traction means, such as at least one guide wire 12, which is fastened or can be fastened to the distal compression ring 6 in a pull resistant manner and which can be slidably received by the proximal compression ring 7 in a manner to allow the distal compression ring 6 to be pulled towards and coupled with the proximal compression ring 7.
  • the anchoring device may further comprise a plurality of needle fasteners 13 protruding from the clamping surface 8 of one of the proximal and distal compression rings 6, 7 towards the other compression ring and adapted to pierce and penetrate the tissue portion 10 clamped therebetween.
  • the needle fasteners 13 improve the anchoring of the lining 2 within the hollow organ 1 and prevent tissue from slipping away from the clamping surfaces 8, 9 both during approximation of the compression rings and after completion of the anchoring.
  • the needle fasteners 13 are configured to be received in corresponding locking seats 14, e.g. internally stepped or riffled holes, formed in the clamping surface 9 of the opposite compression ring (preferably the proximal ring 7) and form one or more barbs 15 which block the needle fasteners 13 inside the locking seats 14 to prevent separation of the interlocked compression rings and to maintain the achieved tissue clamping configuration.
  • the needle fasteners 13 act both as tissue retaining means and as ring locking means.
  • the distal compression ring 6 may comprise a support frame 16 forming a guide seat 17 for a pull resistant connection of the distal compression ring 6 with the guide wire 12, wherein the guide seat 17 is arranged radially inside the distal compression ring 6 at a distance from the tissue clamping surface 8. This allows to manipulate and pull the distal compression ring 6 inside the hollow organ 1 by acting on a guide wire 12, but without interference between the guide wire 12 and the tissue portion 10 intended to be clamped between the compression rings 6, 7.
  • the support frame 1 6 comprises two crosswise (preferably perpendicularly) arranged beams 1 8 bridging the central passage opening 1 1 and connected to respectively diametrically opposite portions of the ring body of the distal compression ring 6.
  • the beams 18 are connected to each other in a connecting region in a centre of a circle defined by the compression ring and this connection region forms the above said guide seat 17.
  • the guide seat 17 may comprise a through hole adapted to slidably receive the guide wire 12 and a clamping jaw or a clamping wedge 19 for locking the guide wire 12 in a pull resistant manner.
  • a locking ring or clip (not illustrated) may be provided which can be fastened to the guide wire 12 to create a local increase of the guide wire thickness which interferes with the shape of the guide seat 17 to lock the guide wire 12 by shape coupling.
  • the distal compression ring 6 comprises ring releasing means which detach the support frame 16 from the distal ring 6 when the pulling force transmitted by the support frame 16 to the ring body of the distal compression ring 6 exceeds a predetermined target value sufficient for an adequate tissue clamping pressure and locking pressure between the compression rings 6, 7.
  • the ring releasing means can be adapted to pulling force-dependently separating the support frame 16 from the distal ring body by resilient radially inward retraction or deformation of the support frame 16, particularly the cross beams 18, or by pulling force-dependently breaking the support frame 16, in predetermined breaking points, preferably near opposite end portions of the cross beams 18. This allows to automatically detach the guide wire 12 together with the support frame 18 from the distal compression ring 6 and withdraw them in proximal direction through the central passage openings 1 1 of the compression rings 6, 7 and endoluminally out of the patients' body.
  • the lining system comprises a lining seat 20 arranged at the distal compression ring 6 and adapted to receive and hold the pliable tubular lining 2 in a packed (substantially ring shaped), e.g. wrapped, folded, compressed or rolled up, configuration with regard to a lining longitudinal extension.
  • the lining seat 20 may co-operate with the support frame 16 to release the lining 2 and, possibly to push at least a portion of the lining 2 distally out of the lining seat 20, when the support frame 16 is detached from the distal ring body.
  • the lining seat 20 may comprise one or more brackets 21 which are directly or indirectly held by the support frame 16 in a retaining position (suitable to retain the packed lining 2) as long as the support frame 16 is coupled to the ring body. Upon detachment of the support frame 16 from the ring body, the brackets 21 move in a release position in which the lining 2 is released to unfold distally.
  • brackets 21 are formed integrally (as a single piece) with the support frame 16.
  • the endoluminal lining system further comprises tissue acquisition means which may be incorporated in the anchoring device 5 or separate from the anchoring device 5.
  • the tissue acquisition means comprise e.g. a plurality of anchoring hooks 30, e.g. so called T-tags, adapted to be fastened to the tissue portion 10 at the anchoring site and flexible pull strings 31 connected to each one of the anchoring hooks 30 and adapted to be extended through the passage opening 1 1 of the proximal compression ring 7 to pull the fastened tissue portion 10 between the tissue clamping surfaces 8, 9 from inside the passage opening 1 1 .
  • An endoluminal applier 26 may be provided for both the tissue acquisition and the fastening of the anchoring device 5.
  • the applier 26 ( Figures 3, 5) has a flexible elongate insertion shaft 27 and a fastening assembly 28 arranged at a distal end 29 of the insertion shaft 27.
  • the fastening assembly 28 includes a fastener driver 32 adapted to hold the anchoring hooks 30 during endoluminal insertion of the applier 26 and operable to drive the anchoring hooks 30, e.g. T-tags into the tissue portion 10.
  • the applier 26 may further comprise a pulling mechanism 33 connected to the pull strings 31 of the anchoring hooks 30 and operable to pull the pull strings 31 into the fastening assembly 28, thereby acquiring the fastened tissue portion 1 0 between the clamping surfaces 8, 9 of the compression rings 6, 7.
  • the applier 26 comprises an instrument channel 34 extending from the fastening assembly 28 to a proximal end of the insertion shaft 27 and adapted to receive the pull strings 31 so that the proximal string ends emerge extracorporeal ⁇ from the proximal end of the applier 26 and can be directly pulled by the doctor.
  • the fastening assembly 28 may further comprise a ring seat 35 adapted to detachably receive the proximal compression ring 7 (for endoluminally inserting the proximal ring to the anchoring site in the hollow organ 1 ) and to support the proximal compression ring 7 while the distal compression ring 6 is pulled against it.
  • the guide wire 12 attached to the distal compression ring 6 may be received in the above described instrument channel 34 of the applier and a proximal guide wire end may be pulled from outside the body in order to approximate the compression rings 6, 7 and lock them together.
  • the applier 26 comprises an endoscope defining the instrument channel 34 and a distal end to which the fastening assembly 28 is attached.
  • the ring locking means comprise at least one pair of diametrically opposite locking pins 22 protruding from one of the distal and proximal compression rings 6, 7 towards the other compression ring and adapted to be received by correspond ing locking seats 14 formed in the other compression ring, e.g. by snap fit, shape connection or interference fit. Both the locking seats 14 and the locking pins 22 may form a guide channel 23, 24 adapted to receive a guide wire 25 which allows the compression rings 6, 7 to be pulled towards each other and in engagement in a tissue clamping configuration.
  • the above described support frame is not necessary and the guide wires 25 are fastened in a pull resistant manner to the locking pins 22, e.g. by means of a wedge or a clamp (not illustrated) adapted to clamp the guide wire against the guide channel 23 and/or a locking ring or clip (not illustrated) which can be fastened to the guide wire 25 to create a local increase of the guide wire thickness which interferes with the shape of the guide channel 23 to lock the guide wire 25 by shape coupling.
  • the locking pins 22 and the corresponding locking seats 14 are formed in the tissue clamping surfaces 8, 9 of the distal and proximal compression rings 6, 7, respectively, and the locking pins 22 are intended to puncture and retain the clamped tissue portion 10 between the compression rings 6, 7.
  • the anchoring device 5 and, hence, the endoluminal lining 2 can be positioned very precisely by pulling or sliding the compression ring 6 with the locking pins 22 along the predefined guide wire path through the hollow organ wall.
  • the insertion of the guide wires 25 along predetermined paths in the lumen wall can e.g. be accomplished by means of a device 36 having a flexible insertion shaft 37 and a guide wire fastening head 38 with an arch shaped hollow needle 39 having a sharp free end suitable to pierce tissue and an internal channel opening near the free end and adapted to receive the guide wire 25.
  • the guide wire fastening head 38 comprises a guide wire feeding mechanism operable to move the needle 39 out of the head 38 along an arch- shaped path in order to pierce the surrounding tissue, feed a portion of the guide wire 25 through the internal channel and, subsequently, withdraw the needle 39 along the arch shaped path back into the head 38, leaving the guide wire portion extended along the thus created path through the pierced tissue ( Figures 9 and 10).
  • each open guide wire loop 40 having a distal guide wire end 41 , a proximal guide wire end 42 (which may at least initially extend outside the body of the patient) and an intermediate guide wire section 43 between the proximal guide wire end 42 and the distal guide wire end 41 which extends along the pierced path through the tissue portion 10 ( Figure 10).
  • each individual guide wire 25 loop 40 is fastened in a pull resistant manner to the locking pins 22 of the distal compression ring 6 and the proximal guide wire end 41 (which emerges extracorporeal ⁇ or which may be grasped by an endoluminal pulling instrument) can be pulled, thereby dragging the distal compression ring 6 from outside the body endoluminally (e.g. through the esophagus, stomach and duodenum) into the hollow organ 1 (e.g. the jejunum) near the target section intended for anchoring the lining 2 ( Figure 1 1 ).
  • the proximal guide wire end 41 By further pulling the proximal guide wire end 41 in a proximal direction, the locking pins 22 of the distal compression ring 6 are pulled from a distal side of the target section 10 into and through the predefined guide wire path within the hollow organ wall.
  • the proximal compression ring 7 can be delivered to the anchoring site and fastened to the tissue portion 10 and to the distal compression ring 6 by means of an endoluminal applier 44 (Figure 12) which is very similar to the previously described applier 26 ( Figure 5).
  • the applier 44 ( Figure 12) comprises a flexible elongate insertion shaft 27 and a fastening assembly 28 arranged at a distal end 29 of the insertion shaft 27.
  • a ring seat 35 adapted to detachably receive the proximal compression ring 7 (for endoluminally inserting the proximal ring to the anchoring site in the hollow organ 1 ) and to support the proximal compression ring 7 while the distal compression ring 6 is pulled against it.
  • the guide wires 25 fastened to the locking pins 22 of the distal compression ring 6 are slidably extended through the corresponding guide channels 24 of the locking seats 14 of the proximal compression ring 7.
  • the applier 44 may comprise an instrument channel 34 extending from the fastening assembly 28 to a proximal end of the insertion shaft 27 and adapted to receive the guide wires 25 so that the proximal guide wire ends 42 emerge extracorporeal ⁇ from the proximal end of the applier 44 and can be directly pulled by the doctor.
  • the ring seat 35 defines a plurality of at least 2 guide wire channels 45 aligned with the guide channels 24 of the locking seats 14 of the proximal compression ring 7 and adapted to slidingly receive the guide wires 25 so that the fastening assembly 28 together with the proximal compression ring 7 are aligned with the predefined guide wire path during ring approximation and press-coupling ( Figures 12 and 13).
  • the press coupling and mutual locking of the compression rings is brought about by pushing the proximal compression ring 7 by the applier 44 distally and contemporaneously pulling the distal compression ring 6 by means of the guide wires 25 in a proximal direction against the proximal ring 7.
  • the applier 44 comprises an endoscope defining e.g. the instrument channel 34 and a distal end to which the fastening assembly 28 is attached.
  • the lining seat 20 may co-operate with the guide wires 25 to release the lining 2 when the guide wires 25 are detached from the distal compression ring 6.
  • the lining seat 20 may comprise one or more brackets 21 which are directly or indirectly held by the guide wires 25 in a retaining position (suitable to retain the packed lining 2) as long as the guide wires 25 are coupled to the distal compression ring 6.
  • the brackets 21 move in a release position in which the lining 2 is released to unfold distally.
  • the brackets 21 are formed integrally (as a single piece) with guide wire locking means 19, e.g. with the above described clamping jaw or a clamping wedge or locking ring or clip which fixate the guide wire 25 to the compression ring.
  • the distal compression ring 6 comprises ring releasing means which detach the guide wire 25 from the distal ring 6 when the pulling force transmitted by the guide wire 25 to the ring body of the distal compression ring 6 exceeds a predetermined target value sufficient for an adequate tissue clamping pressure and locking pressure between the compression rings 6, 7.
  • the ring releasing means can be adapted to pulling force-dependently separating the guide wire 25 from the distal ring body by pulling force-dependently slipping out or tensile failure (rupture) of the guide wire 25 or by pulling force-dependently breaking the locking means 19, in predetermined breaking points. This allows to automatically detach the guide wire 25 from the distal compression ring 6 and withdraw them in proximal direction through the guide channels 23, 24 of the compression rings 6, 7 and endoluminally out of the patients' body.
  • the lining 2 may be automatically released to unfold.
  • Figures 14 through 16 illustrate an exemplary embodiment of onboard tissue acquisition means adapted to acquire the ring shaped tissue portion 10 of the hollow organ 1 between the clamping surfaces of the distal and proximal compression rings 6, 7 during ring approximation without any need of additional tissue acquisition devices and procedures.
  • Such tissue acquisition means may be advantageously used in connection with the anchoring device 5 illustrated in figure 1 .
  • the tissue acquisition means comprise a plurality of needles 46 connected to one of the distal and proximal compression rings 6, 7 and movable, preferably tiltable or rotatable, from a rest position in which pointed free ends 47 of the needles 46 are received inside the ring body of the compression ring, particularly within radially extending grooves 48 formed in the tissue clamping surface 8; 9, and an activated position in which the pointed free ends 47 of the needles 46 protrude radially outward of the compression ring 6 or 7 and are inclined towards the other compression ring, i.e. in the same direction in which the clamping surface faces.
  • the pointed free ends 47 of the needles 46 protrude in the activated position radially outward and distally.
  • the needles 46 are arranged at the distal compression ring 6, the pointed free ends 47 of the needles 46 protrude in the activated position radially outward and proximally.
  • the tissue acquisition can be further improved by moving the needles 46 together with the pierced tissue from the activated position radially inward to an intermediate position between the opposite tissue clamping surfaces 8, 9 of the compression rings 6, 7.
  • the needles 46 are permanently elastically biased towards their activated position and connected to a needle moving mechanism 49 having an adjusting member, e.g. a lever mechanism with an adjusting lever.
  • the adjusting member is adapted to be moved between a resting position in which the needle moving mechanism 49 holds the needles 46 in the rest position and an activating position in which the needle moving mechanism 49 allows the needles 46 to move in the activated position.
  • the adjusting member is locked or actively held in the resting position to hold the needles 46 in the radial grooves 48 and, after positioning of the compression ring 7 near the lining anchoring location in the hollow organ, e.g. in the jejunum, the adjusting member is actively displaced or released to move in the activating position, so that the needles 46 are driven out of the grooves 48 into their activated position.
  • the compression rings 6, 7 or a ring applier may be configured that, during approximation of the distal and proximal compression rings 6, 7, the adjustment member of the needle moving mechanism 49 is displaced from the activating position in the direction of the rest position, so that the needles 46 together with the pierced tissue move from the activated position radially inward to an intermediate position between the tissue clamping surfaces 8, 9 of the compression rings 6, 7.
  • the needle moving mechanism 49 may cooperate with the ring coupling means, e.g. needle fasteners 13 or locking pins 22, with the support frame 16, with a dedicated protrusion formed on the opposite compression ring or with a ring applier for the endoluminal deployment of the lining system.
  • the ring coupling means e.g. needle fasteners 13 or locking pins 22
  • the support frame 16 with a dedicated protrusion formed on the opposite compression ring or with a ring applier for the endoluminal deployment of the lining system.
  • the needle moving mechanism (49) is moved by at least one of the ring locking means and the support frame (16) in a manner to move the needles (46) together with the pierced tissue from the activated position radially inward to the intermediate position.
  • needle fasteners 13 similar to those previously described in connection with figure 1 or locking pins 22 similar to those previously described in connection with figure 7 may be provided at the proximal compression ring 7 or, more generally spoken, at the compression ring opposite the one having the tissue acquisition needles 46.
  • the needle fasteners 13 or locking pins 22 are configured to be received in corresponding locking seats 14, e.g.
  • At least one of the distal 6 and proximal compression ring 7 is time-dependently bio-fragmentable or absorbable. This makes the endoluminal lining a temporary and reversible therapeutic treatment.
  • the tubular lining 2 may be detachably connected to one of the compression rings 6, 7 and can be substituted by another tubular lining, e.g. of different length.
  • the proximal end 3 of the lining 2 may be detachably inserted in a connecting groove 50 of the lining seat 20 formed in one of the distal and proximal compression rings 6, 7 and clamped against the connecting groove 50 by means of a possibly elastically deformable clamping ring 51 having a shape substantially complementary with the shape of the connecting groove 50 ( Figures 15, 16).
  • the anchoring device 5 may be grafted at least partially of bioabsorbable material and the compression rings 6, 7 are substantially rigid, while the guide wires 12, 25 are flexible and substantially inextensible. At least part of the anchoring device 5 may be protected by a protective sheath 60 during endoluminal insertion in the hollow organ 1.
  • Figure 1 9 illustrates an exemplary embod iment of an endolu minal applier 52 for endoluminally delivering and fastening the anchoring device 5 of the lining system to the hollow organ 1.
  • the applier 52 has a flexible insertion shaft 59 extending between a proximal handle (not illustrated) and a distal shaft end at which a ring fastening assembly 28' is provided.
  • the ring fastening assembly 28' comprises a proximal ring holder 53 adapted to hold the proximal compression ring 7, and a distal ring holder 54 adapted to hold the distal compression ring 6.
  • the distal ring holder 54 is translatable relative to proximal ring holder 53 and adapted to cooperate with the proximal ring holder 53 for approximating the proximal and distal compression rings 7, 6 and pressing them together.
  • the ring fastening assembly 28' forms a central channel 55 extending longitudinally through the proximal ring holder 53 and through the distal ring holder 54 and, preferably, opening laterally into a clamping space 56 between the proximal and distal ring holders 53, 54.
  • the central channel 55 is adapted to slidingly receive an endoscope to visualize both the space between the proximal and distal rings 7, 6 received by the corresponding ring holders 53, 54 and the space distally ahead of the ring fastening assembly 28' and, possibly, to slide the applier 52 endoluminally along the endoscope to the lining anchoring site in the hollow organ 1 .
  • the applier 52 assures a correct relative positioning of the compression rings 6, 7 during fastening of the anchoring device 5 and allows an improved guidance through the Gl tract and continuous visualization by the endoscope received in the central channel 55, both during endoluminal insertion and withdrawal of the applier 52 and during fastening of the compression rings 6, 7.
  • the applier 52 comprises a tissue acquisition mechanism 57 adapted to acquire a substantially ring shaped tissue portion 10 of the hollow organ 1 in the clamping space 56 between the proximal and distal ring holders 53, 54.
  • the tissue acquisition mechanism 57 may be arranged in the ring fastening assembly 28' between the central channel 55 and one of the ring holders 53, 54, i.e. radially external of the central channel 55 and radially internal of the ring holder, thereby allowing complete visual access also d uring tissue acq uisition .
  • the tissue acquisition mechanism 57 and the endoscope may be configured to be received together and contemporaneously in the central channel 55, e.g. by passing the tissue acquisition mechanism through an instrument channel of the endoscope while the endoscope is received in the central channel 55 of the ring fastening assembly 28'.
  • the tissue acquisition mechanism 57 may comprise mechanical gaspers or suction means.
  • the distal ring holder 54 comprises ring releasing means which detach the distal ring holder 54 from the distal ring 6 when the force transmitted by the distal ring holder 54 to the ring body of the distal compression ring 6 exceeds a predetermined target value sufficient for an adequate tissue clamping pressure and locking pressure between the compression rings 6, 7.
  • the ring releasing means can be adapted to force-dependently separating the distal ring holder 54 from the distal compression ring 6 by resilient radially inward retraction or deformation of the distal ring holder 54 or by force-dependently breaking the distal ring holder 54 in predetermined breaking points. This allows to automatically detach the distal ring holder 54 from the distal compression ring 6 and withdraw it in proximal direction through the central passage openings 1 1 of the compression rings 6, 7 and endoluminally out of the patients' body.
  • the applier 52 comprises a lining seat 58 arranged at the distal ring holder 54 and adapted to receive and hold the pliable tubular lining 2 in a packed (substantially ring shaped), e.g. wrapped, folded, compressed or rolled up, configuration with regard to a lining longitudinal extension.
  • the lining seat 58 may co-operate with the distal compression ring 6 received by the distal ring holder 54 to release the lining 2 and, possibly to push at least a portion of the lining 2 distally out of the lining seat 58, when the distal ring holder 54 is detached from the distal compression ring 6.
  • bypass conduits can be created in the Gl tract of a patient to achieve a malabsorptive effect in cases where such an effect may enhance weight loss, as well as the initially described effects on hormonal signaling in general.
  • the described devices and procedures help to mimic the effects of gastric bypass in resolution of type 2 diabetes and facilitating weight loss, improve glycemic control and reduce or eliminate other co-morbidities of severe obesity.
  • the described devices and procedures may be advantageously used in conjunction with other therapeutic regimes for the treatment of type 2 diabetes and its co-morbidities and address the patients fear of invasive surgery.
  • the described procedures and devices allow a reversible procedure with an easy removal and replacement of the endoluminal lining or sleeve once the desired effect has been achieved or a modification of the endoluminal lining is desired.

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  • Health & Medical Sciences (AREA)
  • Child & Adolescent Psychology (AREA)
  • Obesity (AREA)
  • Nursing (AREA)
  • Orthopedic Medicine & Surgery (AREA)
  • Engineering & Computer Science (AREA)
  • Biomedical Technology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Vascular Medicine (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Surgical Instruments (AREA)

Abstract

La présente invention concerne un système de revêtement endoluminal pour revêtir de façon interne une section du tractus gastro-intestinal qui comprend un revêtement tubulaire flexible (2) et un dispositif d'ancrage (5) raccordé au revêtement (2). Le dispositif d'ancrage (5) comprend un anneau de compression distal (6) et un anneau de compression proximal (7) initialement séparé de l'anneau de compression distal (6), les anneaux de compression distal et proximal (6, 7) formant une ouverture de passage centrale (11), agissant en coopération sur des surfaces de serrage de tissu opposées (8, 9) et des moyens de verrouillage (13 ; 22) adaptés pour verrouiller l'anneau de compression distal (6) à l'anneau de compression proximal (7) dans une configuration de serrage de tissu.
PCT/EP2011/051814 2011-02-08 2011-02-08 Système de revêtement endoluminal WO2012107079A1 (fr)

Priority Applications (1)

Application Number Priority Date Filing Date Title
PCT/EP2011/051814 WO2012107079A1 (fr) 2011-02-08 2011-02-08 Système de revêtement endoluminal

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
PCT/EP2011/051814 WO2012107079A1 (fr) 2011-02-08 2011-02-08 Système de revêtement endoluminal

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WO2012107079A1 true WO2012107079A1 (fr) 2012-08-16

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Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US9456917B2 (en) 2013-08-28 2016-10-04 Ethicon Endo-Surgery, Inc. Endoscopic transoral duodenal sleeve applier
US10350099B2 (en) 2006-09-01 2019-07-16 Ethicon Endo-Surgery, Inc. Devices and methods for anchoring an endoluminal sleeve in the GI tract

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2004041133A1 (fr) * 2002-11-01 2004-05-21 Valentx, Inc. Appareil et methodes permettant de traiter l'obesite morbide
US7220237B2 (en) 2002-10-23 2007-05-22 Satiety, Inc. Method and device for use in endoscopic organ procedures

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7220237B2 (en) 2002-10-23 2007-05-22 Satiety, Inc. Method and device for use in endoscopic organ procedures
WO2004041133A1 (fr) * 2002-11-01 2004-05-21 Valentx, Inc. Appareil et methodes permettant de traiter l'obesite morbide

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US10350099B2 (en) 2006-09-01 2019-07-16 Ethicon Endo-Surgery, Inc. Devices and methods for anchoring an endoluminal sleeve in the GI tract
US9456917B2 (en) 2013-08-28 2016-10-04 Ethicon Endo-Surgery, Inc. Endoscopic transoral duodenal sleeve applier
US10307280B2 (en) 2013-08-28 2019-06-04 Ethicon Endo-Surgery, Inc. Endoscopic transoral duodenal sleeve applier

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