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
  • A61F5/0013—Implantable devices or invasive measures
  • A61F5/003—Implantable devices or invasive measures inflatable
• • 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
  • A61F5/0079—Pyloric or esophageal obstructions

Definitions

• the present invention relates to the field of devices for inser tion into the gastro-intestinal tract and for anchoring at the pylorus.
• the device may be a by pass tube for bypassing a portion of the bowel, or a plug for plugging the pylorus.
• Surgical techniques include creation of gastric pockets and gastric bypasses of the stomach, duodenum and part of the jejunum.
• Bypass tubes or liners have been proposed for insertion into the gastro-intestinal tract, to bypass the duodenum and optionally part of the jejunum.
• a first aspect of the disclosure provides a gastric anchor for anchoring a tube with respect to a pylorus of a patient, the tube having a distal end for placement within the small intes tine and a proximal end for placement near or at the pylorus and/or within the stomach, the gastric anchor serving to prevent distal migration of the proximal end, the gastric anchor com prising a tubular balloon and a self-expanding structure, the gastric anchor having: a first end for seating on the gastric side of the pylorus; a first region having a first resistance to inward collapsing; and a second region having a second smaller resistance to inward collapsing, the first region being closer than the second region to the first end.
• Such a configuration can provide a gastric anchor that has tai lored resistances to collapsing.
• the second region can be rela tive conformable to accommodate contractions of the stomach and/or antrum and reduce risk of the contractions dislodging the anchor in a proximal direction.
• the second region can permit inward collapsing to a degree allowing digested food (e.g. chyme) to pass from the stomach to the duodenum.
• the first re gion can be relatively firm to ensure that gastric anchor will retain a sufficient size to obstruct distal migration through the pylorus even when the first region of the gastric anchor collapses at least partly inwardly under the influence of a stomach contraction.
• the different first and second resistances to collapsing are provided at least partly by the self-expanding structure.
• the self-expanding structure may comprise a first zone having first zone resistance to inward collapsing, and a second zone with a smaller second zone resistance to inward col lapsing .
• the self-expandable structure may have any desired form.
• it may comprise a stent or stent-like structure. It may define a framework of struts and/or cells.
• the first zone of the self-expanding struc ture may comprise an annular hub or collar, and/or the second zone of the self-expanding structure may comprise a plurality of independently deflectable limbs or beams extending from the first zone.
• a closely related second aspect of the disclosure provides a gastric anchor for anchoring a tube with respect to a pylorus of a patient, the tube having a distal end for placement within the small intestine and a proximal end for placement near or at the pylorus and/or in the stomach, the gastric anchor serving to prevent distal migration of the proximal end, the gastric anchor comprising a tubular balloon and a self-expanding structure for biasing a radially inner wall and/or a radially outer wall of the tubular balloon outwardly, towards its enlarged form, the self-expanding structure comprising a first zone comprising an annular hub or collar, and a second zone comprising a plurality of independently deflectable beams or limbs extending from the first zone.
• the self-expanding structure may be attached to and/or embedded within one of the walls, for example, the ra dially outer wall, to draw the wall into contact with the sur rounding stomach wall.
• the independently deflectable beams/limbs can provide conformability, and/or the annular hub/collar, where provided, can provide greater structural re sistance to inward bending or collapsing.
• Each independently deflectable beam/limb, where provided, may comprise single elon gate rib or strut, or it may comprise plural struts collectively defining the beam or limb shape.
• the tubular balloon may have any desired exterior shape or profile for fit ting within the pyloric antrum and/or stomach. Suitable shapes include, for example, a cup-shape, a tulip-shape, a bell-shape, a pear-shape, a tear-drop shape, a funnel-shape, an umbrella- shape.
• the tubular balloon can includes an internal channel, and an entrance mouth for admitting chyme into the channel to pass through the anchor towards the pylorus.
• the balloon may serve to occupy space for gastric restriction. Additionally or alter natively, the balloon may take some of the load from the self expanding structure, and reduce risk of the structure becoming fatigued, or fracturing, or causing a central gastro-duodenal obstruction .
• the deflectable beams/limbs can deflect inward ly to allow local inward collapsing of the balloon to accommo date stomach/antrum contractions, and permit chyme to pass to the duodenum, as explained above.
• the deflectable limbs/beams are biased outwardly to urge the balloon to re-expand, and to follow movement of the stomach wall, when the contraction is over.
• the hub/collar may comprise a plurality of struts defining a structure of cells.
• the hub or collar may comprises at least one row of cells, optional ly two rows, or more.
• the hub/collar may provide a stronger (e.g. radially stronger) structure than the deflectable beams/limbs, to ensure that the end of the gastric anchor closer to the pylorus remains sufficiently large to avoid accidentally migration through the pylorus and into the duodenum, even in the presence of strong stomach contractions.
• the axial length of the hub/collar can be dimensioned such that the beams/limbs may be positioned where highest antral motility strains occur.
• the self expanding structure may have any desired form.
• it may comprise a stent or stent-like structure. It may define a framework of struts and/or cells.
• Each independently de flectable beam/limb where provided, may comprise single elon gate rib or strut, or it may comprise plural struts collectively defining the beam or limb shape.
• the radial thickness of the tubular balloon may be generally constant around the axis of the balloon and/or the channel, but this is not essential.
• the balloon walls may be of substantially inelastic material, such that the balloon wall material does not stretch under normal inflation of the balloon. Additionally or alternatively to any of the above, the balloon may have a volume in the range of 200mL - 500mL. The balloon may optionally serve as a gastric occupying component to reduce the volume of the stomach for food.
• At least the gastric anchor and optionally the pyloric anchor as a whole is collapsible to a non-deployed configuration for introduction through the stomach towards the pylorus, and is expandable to a deployed configuration for anchor at or near the pylorus.
• the self-expandable structure where provided,
• the balloon may be inflated with any suitable fluid, such as a gas (e.g. air) or a liquid (e.g. saline).
• a gas e.g. air
• a liquid e.g. saline
• the infla tion pressure is optionally not greater than 2 atm, optionally not greater than 1.75 atm, optionally not greater than 1.5 atm, optionally not greater than 1.25 atm, optionally about 1 atm (for example, which corresponds generally to pressure equilibri um with ambient pressure within the stomach).
• a closely related third aspect of the disclosure provides a method of deploying a gastric anchor for anchoring a tube with respect to a pylorus of a patient, the tube having a distal end for placement within the small intestine and a proximal end for placement near or at the pylorus, the gastric anchor serving to prevent distal migration of the proximal end, the gastric anchor comprising a tubular balloon and a self-expanding structure, the method comprising the steps of:
• a pressure selected as one or more of: a pressure that does not prevent at least partial inward collapsing of the tubular balloon in response to stomach contractions; a pressure not greater than 2 atm; a pressure not greater than 1.75 atm; a pressure not greater than 1.5 atm; a pressure not greater than 1.25 atm; a pressure about 1 atm; and
• a fourth aspect of the invention optionally including any of the aforementioned aspects and features, provides an anchor (e.g. a pyloric anchor) for anchoring a device with respect to a pylorus of a patient.
• the anchor comprises a frame extending around an axis, the frame being transformable from a non- deployed configuration for introduction to the pylorus, towards a deployed configuration for anchoring at the pylorus.
• the frame is configured such that transformation from the non- deployed configuration towards the deployed configuration causes a first portion of the frame to at least partly twist around the axis relative to a second portion of the frame.
• the first portion of the frame that twists may be an intermedi ate frame portion disposed, at least in the deployed configura tion, between the second frame portion and a third portion of the frame.
• a closely related fifth aspect of the disclosure provides an anchor comprising a frame extending around an axis, the frame including a first intermediate portion disposed axially between second and third portions, the frame having a non-deployed configuration for introduction to the pylorus and a deployed configuration for anchoring at the pylorus and in which struts of the first portion are biased to extend predominantly in the same direction as one another twisting at least partly around the axis to torsionally couple the second portion to the third portion.
• struts of the first portion may be less twisted around the axis than in the deployed config uration, optionally extending substantially axially without twisting around the axis.
• the frame may be deformable to the non-deployed configuration, and be self-biasing to transform from the non-expanded configu ration to the expanded configuration.
• the second and third frame portions are anchor por tions for engaging tissue on either side of the pylorus, and the first portion is a bridging portion for passing within the pylo rus.
• the first portion may cause relative angular displacement around the axis, between the second and third portions when the frame transforms towards the deployed configuration. Additionally or alternatively, transformation from the non-deployed configura tion towards the deployed configuration causes the first and second portions of the frame to move axially closer to each oth er, optionally to bias at least one, optionally both, of the second and third portions to bear axially against the pylorus.
• Such configurations can preload the frame, and enable loads and/or displacements to be converted between axial and rotation al senses.
• the twisting action and/or torsional configuration can bias the second and third portions axially towards each oth er, to compress the pylorus axially.
• Axial displacement between the second and third portions can be accommodated by partial twisting (or partial untwisting) motion, without detracting from the anchoring effect.
• bypass tube may be provided with actuation means for setting or changing the amount of twisting between the gastric anchor and the duodenal anchor.
• actuation means for setting or changing the amount of twisting between the gastric anchor and the duodenal anchor.
• the open passage of the by pass tube may be dynamically changed or individually set by set ting a specific twisting angle, during or after implantation.
• the actuation means can e.g. gradually change the axial length between the duodenal and the gastric anchor.
• An axial change in the length induces a twisting motion, due to the twisting struts and thereby a reduction of the open passage.
• the actuation means can be mechanically operated means, actuated during implantation, e.g. be means of axially or circumferen tially acting on pull wires or the like or by a threaded, actua- table connection between the two anchors.
• the actuation means could also be actuateable after implantation and be made e.g. in the form micro-electro-mechanical systems, motors or in the form of magnetically driven components.
• the actuation means can be mechanically operated during implan tation.
• the through-passage may be dynamically controlled based e.g. parameters such as food intake, physiolog ical parameters or habits of the patient.
• a torus shaped component that can be placed in the most proximal section of the duodenum (duo denal bulb) or elsewhere within the GI tract such as in the most distal part of the stomach in the antrum (right before the pylo rus).
• This can be a separated component or it can form an an chor.
• There can also be two tori each sitting on one side of the pylorus.
• the torus, or tori can be filled with a fluid (gas or liquid), e.g. from a reservoir floating in the stomach.
• Filling can also be done or triggered remotely.
• the reservoir is emptied and when the torus is not filled and wide open, the reservoir is full.
• This alternative embodiment also allows to control (disturb, acceler ate, slow) gastric emptying and have an effect on hunger, sa tiety, and ultimately weight loss.
• one of the second and third portions may be more rigid than the other, such that the more- rigid portion may be expected to rotate locally less than the other.
• the second portion in the duodenum may be more rigid than the third gastric portion in the stomach.
• the third gastric portion in the stomach may be more rigid than the second portion in the duodenum.
• the first portion in the deployed configuration, defines a waist between the second and third portions. Twisting can increase a peripheral (e.g. circumferential) sepa ration between two points on the frame, causing the frame to waist inwardly to a smaller lateral (e.g. radial) dimension to accommodate the increased peripheral (e.g. circumferential) sep aration.
• a peripheral e.g. circumferential
• lateral e.g. radial
• one of the first and second portions may optionally have a larger lateral dimension (e.g. diameter) and/or axial dimension (e.g. axial length) than the other of the portions.
• the self-deploying frame may, for example, be made of a shape memory alloy, for example, an alloy comprising nickel (Ni) and titanium (Ti), optionally also comprising cobalt (Co).
• the shape memory alloy may be or comprise nitinol.
• the frame may comprise a lattice of interconnected frame struts and/or a braided wire structure
• the frame may be biased towards its deployed configuration (for example, by heat setting the frame in the deployed configura tion), and be deformable to its non-deployed configuration for loading into, for example, a sheath. Upon removal from the sheath, the frame can self-deploy to the deployed configuration by virtue of a shape memory effect.
• Configuration of frame using any of the above features can pro vide a versatile frame geometry that can be configured for dif ferent applications.
• the degree of inward waisting of the twisting first portion can be controlled by the degree of twist around the frame axis. The greater the angle of twist, the nar rower the waist.
• the degree of twisting can be one of the pa rameters used during heat setting to determine the shape of the frame in the deployed configuration.
• the frame can be configured with a large twisting angle around the axis to substantially pinch the centre of the frame closed.
• the frame can be configured with sufficient twist to form a waist between the first and second anchor regions, leav ing open a sufficiently large through-passage to allow passage of chyme.
• the frame may be provided on its interior surface and/or its exterior surface, or be coated, with liner material.
• Suitable liner material may comprise biological tissue (for ex ample, pericardial tissue) or synthetic polymeric material (for example, polyurethane or PTFE).
• the material may be provided in sheet form, film form, a coating, or as a woven fabric or a non- woven fabric.
• Liner material on the interior surface can provide an inner con duit, or an inner seal in the case of a pyloric plug.
• Liner ma terial on the exterior surface can enhance atraumatic fitting of the anchor with respect to anatomical tissue at and/or on either side of the pylorus, and avoid direct contact between the frame and the anatomical tissue should this be desirable.
• the disclosure also pro vides a device for fitting at least partly at a pylorus of a pa- tient.
• the device can comprise an anchor including any one or more of the features above.
• the device may, optionally, be a pyloric plug, or a duodenal tube.
• the gastric anchor may correspond to, and/or constitute, the second and/or third por tion of the fourth and/or fifth aspect.
• a closely related sixth aspect of the invention provides a meth od of deploying a pyloric anchor at a pylorus of a patient, the anchor optionally according to the fourth and/or fifth aspect, the anchor comprising a frame extending around an axis, the method comprising:
• the step of causing twisting may comprise releasing a self deploying frame to twist as the frame self-deploys from the non- deployed configuration to the deployed configuration.
• the step of causing the frame to twist may comprise for cibly twisting the frame by application of a twisting force to the frame.
• a seventh aspect of the present disclosure optionally in combi nation with any of the preceding aspects, comprises a bypass tube for placement into the small intestine of a patient, the bypass tube made of flexible material and having a longitudinal axis, the bypass tube having a radially compressed configuration for introduction, and a radially expanded configuration for functional implantation, the tube carrying a reinforcement ele ment for reinforcing the flexible tube, the reinforcing element having a non-helical shape.
• Non-helical reinforcement element can avoid complica tions caused by a helical shape tending to lengthen axially when compressed radially, and foreshorten axially when expanding ra dially. Such changes in axial length can apply additional stresses to the flexible tube, especially when made of inelastic material.
• the reinforcement element has a shape com prising circumferentially expandable and collapsible rows, in terconnected by at least one substantially axial connecting seg ment.
• Each row may, for example, comprise a reinforcement pattern ex tending generally in a circumferential direction of the tube.
• the row may extend around the entire circumference (e.g. around 360° of the circumference), or only partially around the circum ference (e.g. around about 180° of the circumference).
• Using a partial circumference may leave a portion of the flexible tube unreinforced, and able to conform to movements of the small in testine, for example, peristaltic movements for advancing chyme.
• Each row may optionally have a zig-zag or sinuous reinforcement pattern.
• Such a pattern can be compressible and expandable in the circumferential direction, without changing axial dimension substantially .
• the axial segment(s) also need not change length during radial compression and expansion, because the axial segment(s) is gen erally perpendicular to the direction of changing dimension.
• the tube may have a length for extending from the pylorus into the duodenum, and optionally into the jejunum.
• the reinforcement may serve to limit the free movement of the tube so as to avoid twisting or kinking of the tube.
• the rein forcement may be present throughout the tube and/or be restrict ed to individual regions; and the reinforcement may be in and/or on the tube. Twists in a bypass tube can limit the flow of gas tric content toward the bowel; this in turn can lead to the dis comfort of the patient. In cases of extreme twisting, the tube can become completely blocked and obstruct the passage of any gastric content.
• the reinforcement confers a certain firmness to the tube thus avoiding twisting and/or blockages due to kinking.
• the reinforcement may be made of any suita ble material such as metal and preferably Nitinol. Said rein forcement may be situated in and/or on the tube.
• the above reinforcement may comprise at least one repetitive pattern.
• Said repetitive pattern may be at least one continuous triangular pattern and/or sinusoidal pat tern and said repetitive pattern may run along the circumference of the tube. The use the repetitive pattern allows the tube to compress circumferentially when necessary whilst ensuring firm ness around the reinforcement.
• the reinforcement may consist of at least one circumferential and/or partially circumferential row of repetitive reinforce- ment, for example, the reinforcement may expand over 380° or over 180° of the tube.
• the reinforcement structure may com prise at least one repetitive reinforcement pattern arranged in at least one row.
• sections of the repetitive reinforcement pattern running over at least at portion of the circumference of the tube may be positioned on alternate opposite sides.
• a self deploying and/or self-expanding structure and/or frame and/or reinforcement can avoid the need to forcibly deploy the struc ture or frame using a special delivery tool. It can also permit the devices and/or anchors to be easily retrievable after im plantation when their function is no longer desired or when the device reaches the end of its functional life. It can also per mit the devices and/or anchors and/or reinforcement to be de formable have resilience to better perform their function in the mobile environment of the stomach and small intestine. However, if preferred, a non-self-deploying material may be used for the frame or structure or reinforcement.
• a self-deploying frame or structure may, for example, be made of a shape memory alloy, for example, an alloy comprising nickel (Ni) and titanium (Ti), optionally also comprising cobalt (Co).
• the shape memory alloy may be or comprise nitinol.
• the frame may comprise a lattice of interconnected frame struts and/or a braided wire structure
• the duodenal side of a pyloric anchor may have an outer diameter in a range of about 3cm to about 4cm.
• the gastric side of a pyloric anchor may have an outer diameter in a range of about 4cm to about 6cm, optionally about 5cm.
• the tubular balloon may have a radial wall thickness of about 1.5cm to about 2cm, or a total diametric wall thickness of about 3cm to about 4cm.
• the hollow channel inside the tubular balloon may have a diameter of about 1cm to about 3cm, optionally about 2cm. The diameter may depend on the degree of gastric restriction de sired for slowing flow of chyme out of the stomach.
• the twisted portion of the frame may have an inner diameter of a few mm, for example, up to 5mm or less.
• the inner diameter of the twisted portion may be in the range of about 1 cm to about 3 cm, optionally about 2cm.
• the apparatus or a component of the apparatus may optionally be formed by additive manufacturing / three-dimensional printing.
• Fig. 1 is a schematic side view of a bypass tube having a pylo ric anchor
• Fig. 2 is a schematic side view showing detail of Fig. 1;
• Figs. 3a and 3b are schematic side views illustrating how the anchor absorbs stomach and/or antral contractions;
• Fig. 4 is a schematic side view of a pyloric anchor in a non- deployed configuration
• Fig. 5 is a schematic side view of the pyloric anchor of Fig. 4 in a fully deployed configuration
• Fig. 6 is a schematic side view of the pyloric anchor of Figs. 4 and 5 in an implanted configuration
• Fig. 7 is a schematic side view illustrating the anchor forming a pyloric plug
• Figs. 8a and 8b are schematic views of an alternative embodiment of the pyloric plug and
• Figs. 9a and 9b are schematic views of another alternative em bodiment of the pyloric plug.
• a first embodiment of device for insertion into the gastro-intestinal tract comprises a pyloric anchor 10 for anchoring at or with respect to a pylo rus 12 of a patient, and a bypass tube 14 extending distally from the anchor 10.
• the pyloric anchor includes a self-deploying and/or self expanding frame 16 including a first portion 18 at the pylorus, a second portion 20 in the form of a duodenal anchor, and a third portion 22 in the form of a gastric anchor.
• the gastric anchor serves to resist migration in a direction out of the stomach and through the pylorus 12.
• the duodenal anchor serves to resist migration from the duodenal side into the stomach.
• the third portion 22 includes an annular shaped hub or collar 22a from which extend a plurality of independently deflectable limbs 22b.
• the gastric anchor further includes a tubular or to rus balloon 24 having a shape suitable for seating in the pylo ric antrum, such as by way of example, umbrella-shaped, or tu lip-shaped.
• the balloon can serve as a gastric occupying compo nent to reduce the volume of the stomach to food, and/or a gas tric restriction with a passage dimensioned to restrict flow of chyme out of the stomach to the duodenum.
• the third portion 22 of the frame serves to bias the balloon 24 into engagement with the stomach wall.
• the deflectable limbs 22b permit the mouth region of the gastric anchor to collapse locally at least partly in wardly, and thereby accommodate and/or absorb the stomach con traction without pulling or jerking the gastric anchor proximal- ly.
• the hub or collar 22a is slightly stiffer, and provides a stable portion of the gastric anchor of large enough diameter to ensure that the gastric anchor will not pass accidentally through the pylorus even when the deflectable limbs 22b are be ing compressed inwardly.
• the second portion 20 forming a duodenal anchor may have a gen erally cylindrical shape, and/or have length not longer than the duodenal bulb.
• the second portion can be laser-cut or braided. Howsoever formed, in the illustrated embodiment, the first, sec- ond and third portions of the frame are optionally integral with one another and form a single body and/or unitary frame.
• the frame 16 extends around an axis 28.
• the frame 16 is self-deployable from a non-deployed configuration (Fig. 4) towards a deployed (e.g. fully deployed) configuration (Fig. 5) for anchoring at the pylorus.
• a deployed configuration e.g. fully deployed
• the frame 16 might not reach the fully deployed configuration, but instead achieve equilibrium with the pylorus and surrounding anatomy in a slightly compressed or implanted configuration in which the frame 16 continues to bias towards the fully deployed configura tion.
• the first portion 18 is configured to twist at least partly around the axis 28 when the frame trans forms from the non-deployed configuration towards the deployed configuration.
• the first portion 18 comprise a plurality of struts extending predominantly in the same direction as each other to at least partly twist around the axis, and to torsion- ally couple the second portion 20 to the third portion 22. Twisting generates a rotational or torsional preload against the pylorus. This rotational preload resists axial migration by translating axial mechanical movement and/or force into rota tional movement and/or force (as indicated by arrows 30).
• the second and third portions can main tain a bias force against the pylorus from either side.
• the tube 14 comprises a support or rein forcement 34 present in and/or on the tube 14.
• the reinforce- ment is intended to prevent the flexible tube material from twisting or pinching or kinking within the small intestine.
• the reinforcement has a nonhelical shape, optionally comprising rows of repeating patterns (e.g. zig-zag or sinusoidal) extending circumferentially completely or partly around the tube circum ference, to allow radial compression and expansion without sub stantial axial length changes, and interconnected by axial join ing segments.
• the frame 16, and the reinforcement 34 may be made of shape memory alloy, for example, nitinol.
• the frame 16 may be heat- set in the deployed (e.g. fully deployed) and twisted configura tion, and be deformable (e.g. compressible) to the non-deployed configuration for introduction using a delivery sheath 40. Upon removal of the sheath 40, the frame self-deploys towards the de ployed configuration until implantation equilibrium is reached.
• the balloon 24 may be inflated to a suitable pressure to assist anchoring and occupy space within the stomach, but not too high that the inflation pressure will interfere with ability of the gastric anchor to accommodate or absorb stomach contractions.
• a further feature is that the frame geometry is versatile in that can be configured for different applications.
• the degree of inward waisting of the first portion 18 can be controlled by the degree of twist around the frame axis 28. The greater the angle of twist, the narrower the waist.
• the degree of twisting can be one of the parameters used during heat setting to deter mine the shape of the frame 16 in the deployed configuration.
• the frame can be configured with sufficient twist to form a waist between the first and second anchor regions, leaving open a suf ficiently large through-passage to allow passage of chyme.
• the frame can be con figured with a large twisting angle around the axis to substan tially pinch the centre of the frame closed.
• the plug embodiment may be used to complement a gastro-intestinal tract diversion, such as a gastro-jejunal diversion.
• Figs. 8a and 8b schematically show a pyloric plug which is be provided with actuation means for individually setting the de gree of twist and hence the cross-section of the through- passage.
• a distance dl between the second portion 20 and the third portion 22 is larger than a distance d2 in Fig. 8b.
• the actuation means in Fig. 8a and 8b are schematically shown in the form of a sleeve 32 on portion 22 and a stem 31 rotationally mounted on portion 20.
• the sleeve 32 as an inner thread, in which engages an outer thread of the stem 21.
• the distance be tween portion 20 and 22 can be changed by screwing the stem 31 into the sleeve 32.
• the frame 16 may be coated, e.g. polymer coated, to form liner material 26, and/or to integrate with a wall of the balloon 24 (e.g. when used with a bypass tube).
• the liner material 26 can reduce any traumatic effect of the frame bearing against anatomical tissue.
• the liner material 26 could also be placed internally, specifically inside the first portion 18 of the frame, optionally creating bulky folds of the material by design when the frame is in the deployed configuration. This feature could be especially useful for a device in the form of a pyloric plug that occludes the pylorus as a complimentary device in the case of creation of gastro-jejunal diversion (not shown).
• Fig. 9a and 9b show still another embodiment of a pyloric plug which is provided with actuation means for dynamically setting the cross-section of the through-passage.
• the pyloric plug is provided with an inflatable, toroidal duodenal anchor 20.
• the through-passage is reduced from PI in fig 9a to P2 in fig 9b. This change is made by increasing the amount of a fluid within a hollow cavity of the toroidal anchor 20.
• This increase can be achieved by transferring a fluid (e.g. a gas or a liquid) from a reservoir 35 placed in the stomach to the cavity of the anchor 20 via a conduit 33.
• a fluid e.g. a gas or a liquid
• Such a transfer can be passive, by the content of the stomach acting on the res ervoir 35 and increasing the pressure in the reservoir 35. It can also be actively triggered, e.g. by a an implanted pump (not shown) arranged in the conduit 35.
• a pump again could be actuated via a remote control or with a control receiving sensor inputs relating to patent parameters or behaviour.
• duodenal anchor 20 can replace the anchor 20 shown in the other embodiments.
• gastric anchor 22 could also be replaced by an inflatable toroidal anchor. It is also conceiva ble to add toroidal inflatable members to the anchor(s) 20 and 22 shown in the previous embodiments.

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• 2021
  • 2021-07-09 EP EP21315125.1A patent/EP4115855A1/en not_active Ceased
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