INTRALUMINAL DEVICE AND METHOD WITH ANTI-MIGRATION

Abstract

An intraluminal device and method of resisting migration of a device in a lumen, the lumen having muscle defining an intraluminal sphincter includes a device having a body with a size and shape of a portion of the lumen. The device further includes at least one tine extending distally from the body. The at least one tine is rigid or semi rigid. The device is deployed in the lumen with the body proximal the sphincter with respect to peristaltic movement of the lumen and with the at least one tine penetrating the muscle of the sphincter to resist distal migration.

Claims

1. A method of resisting migration of a device in a lumen, said lumen having an esophagus, a stomach and a muscle defining the gastro-esophageal (EG) sphincter between the esophagus and the stomach, said method comprising: said device having a body with a size and shape of a portion of the lumen wherein said device body is coupled with another body with a connector, wherein said body comprises an esophageal member configured to the size and shape of the distal portion of the esophagus wherein said another body comprises a cardiac member distal of the gastro-esophageal (EG) sphincter and configured to the size and shape of a portion of the cardiac portion of the stomach wherein said connector passes through the and EG sphincter the device further includes at least one tine extending distally from the body, said at least one tine being rigid or semi rigid, wherein said at least one tine is configured to penetrate the muscle of the EG sphincter sufficiently to resist separation of the at least one tine from the muscle due to peristalsis; and deploying the device in the lumen with the body proximal the sphincter with respect to peristaltic movement of the lumen with the at least one tine penetrating the muscle of the sphincter.

2. The method as claimed in claim 1 wherein said at least one tine comprises at least two tines that are axially spaced around the body with respect to the lumen.

3-4. (canceled)

5. The method as claimed in claim 41 wherein said deploying the device comprises (i) compressing the body and the another body in a deployment device, (ii) positioning the deployment device at least partially distal of the sphincter and deploying the another body from the deployment device distal of the sphincter, (iii) moving the deployment device proximally and deploying the body and the at least one tine proximal of the sphincter and (iv) further deploying the device from the deployment device and allowing subsequent movement of the device causing the at least one tine to penetrate the sphincter.

6. The method as claimed in claim 5 wherein at least one selected from said connector and said another device is sufficiently flexible in order to perform (iii) while maintaining said another body distal to said sphincter.

7-10. (canceled)

11. The method as claimed in claim 1 wherein said at least one tine is directed distally and outwardly, but more distally than outwardly.

12. The method as claimed in claim 11 wherein said at least one tine is directed distally and outwardly at angle between said at least one tine and a central axis of said body between approximately 5 degrees and approximately 45 degrees.

13. The method as claimed in claim 1 wherein said at least on tine has a length of between approximately 0.5 cm and approximately 2.0 cm.

14. The method as claimed in claim 1 including an enlarged tip of said at least one tine to resist catching on a surface.

15. The method as claimed in claim 1 wherein said at least one tine is configured to be retained entirely within said lumen.

16-28. (canceled)

29. An intraluminal device that is adapted to be deployed in a lumen that experiences peristaltic waves and has muscle defining an intraluminal sphincter, said device comprising: an esophageal member having a size and shape of a portion of the distal portion of the esophagus and at least one tine extending distally from the esophageal member, said at least one tine being rigid or semi rigid; and said at least one tine adapted to penetrate the muscle of the esophageal-gastric (EG) sphincter when the esophageal member is deployed in the esophagus upstream of the EG sphincter; and a cardiac member having a size and shape of the cardiac portion of the stomach coupled with said esophageal member with a connector, said connector configured to cause said cardiac member to apply stress to the cardiac portion of the stomach when said connector passes through the EG sphincter and said cardiac member is in the stomach.

30. The device as claimed in claim 29 wherein said at least one tine comprises at least two tines that are axially spaced around the esophageal member.

31. The device as claimed in claim 29 wherein the at least one tine is configured to penetrate the muscle of the sphincter sufficiently to resist separation of the at least one tine from the muscle due to peristalsis.

32. The device as claimed in claim 29 wherein at least one selected from said connector and said cardiac member is sufficiently flexible in order to allow the esophageal member to be displaced proximally sufficiently to allow said at least one tine to engage the muscle of the EG sphincter.

33. The device as claimed in claim 31 wherein the at least one tine is configured to penetrate the muscle of the sphincter sufficiently to resist separation of the at least one tine from the muscle due to peristalsis.

34. The device as claimed in claim 29 wherein said at least one tine is directed distally and outwardly but more distally than outwardly.

35. The device as claimed in claim 34 wherein said at least one tine is directed at an angle between said at least one tine and a central axis of said body between approximately 5 degrees and approximately 45 degrees.

36. The device as claimed in claim 29 wherein said at least one tine has a length of between approximately 0.5 cm and approximately 2.0 cm.

37. The device as claimed in claim 29 including an enlarged tip of said at least one tine.

38. The device as claimed in claim 29 wherein said at least one tine is configured to be retained entirely within the lumen.

39. The method as claimed in claim 1 including explanting the device including moving the at least one tine to not extend outwardly from the body.

40. The method as claimed in claim 39 wherein said device includes a removal ring at a proximal end portion of the body and a retraction ring at a distal end portion of the body that is connected with said removal ring wherein proximal force applied to said reremoval ring causes said retraction ring to move the at least one tine inwardly.

41. The method as claimed in claim 40 wherein said traction ring moves said at least one tine inwardly by at least one selected from (i) reducing a diameter of said distal end portion of said body (ii), pulling inwardly on said at least one tine, and (iii) retracting said at least one tine into a pouch.

42. An intraluminal device that is adapted to be deployed in a lumen that experiences peristaltic waves and has muscle defining an intraluminal sphincter, said intraluminal device comprising: an esophageal member having a size and shape of a portion of the distal portion of the esophagus and at least one anchor extending distally from the esophageal member and adapted to resist distal migration of said esophageal member; and said at least one anchor comprising a base extending distally from the esophageal member and at least one tine extending distally from the base, said base adapted position said at least one tine to penetrate the muscle of the esophageal-gastric (EG) sphincter when the esophageal member is deployed in the esophagus upstream of the EG sphincter and said base adapted to allow lateral motion of the tine with respect to said esophageal member; and a cardiac member having a size and shape of the cardiac portion of the stomach coupled with said esophageal member with a connector, said connector configured to cause said cardiac member to apply stress to the cardiac portion of the stomach when said connector passes through the EG sphincter and said cardiac member is in the stomach.

43. The intraluminal device as claimed in claim 42 wherein said at least one anchor comprises a plurality of said anchors distributed around a perimeter of said esophageal member.

44. The intraluminal device as claimed in claim 42 wherein said at least one tine has a length sufficient to penetrate to the muscularis of the EG sphincter without penetrating outside of the lumen.

45. The intraluminal device as claimed in claim 42 wherein said at least one tine comprises at least two tines.

46. The intraluminal device as claimed in claim 45 wherein said at least two tines are angular with respect to each other.

47. The intraluminal device as claimed in claim 42 including an enlarged diameter of said at least one tine that is adapted to resist withdrawal of said at least one tine from the muscle of the EG sphincter.

48. The intraluminal device as claimed in claim 47 wherein said enlarged diameter is shaped as a sphere or a triangle.

49. The intraluminal device as claimed in claim 42 wherein said base is pivotally mounted to said body.

50. The intraluminal device as claimed in claim 42 wherein said esophageal member comprises a mesh and a flexible cover over said mesh and wherein said base comprises an extension of said mesh and said flexible cover.

51. The intraluminal device as claimed in claim 50 wherein said mesh comprises a metal.

52. The intraluminal device as claimed in claim 51 wherein said metal comprises nitinol.

53. The intraluminal device as claimed in claim 50 wherein said flexible cover comprises a silicone.

54. A method of resisting distal migration of an intraluminal device that is deployed in a lumen that experiences peristaltic waves and has muscle defining an intraluminal sphincter, said intraluminal device having an esophageal member having a size and shape of a portion of the distal portion of the esophagus, a cardiac member having a size and shape of the cardiac portion of the stomach coupled with said esophageal member with a connector, said connector configured to cause said cardiac member to apply stress to the cardiac portion of the stomach when said connector passes through the EG sphincter and said cardiac member is in the stomach, said method comprising: having at least one anchor extending distally from the esophageal member and adapted to resist distal migration of said esophageal member; said at least one anchor comprising a base extending distally from the esophageal member and at least one tine extending distally from the base, and said base positioning said at least one tine to penetrate the muscle of the esophageal-gastric (EG) sphincter when the esophageal member is deployed in the esophagus upstream of the EG sphincter and said base allowing lateral motion of the tine with respect to said esophageal member in response to operation of the EG sphincter.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

[0031] FIG. 1 is a side elevation of an intraluminal device according to an embodiment of the invention;

[0032] FIG. 2 is a view of the intraluminal device in FIG. 1 deployed to the GI tract of a recipient an positioned at the esophageal-gastric sphincter (ESP) of the recipient;

[0033] FIG. 3 is the save view as FIG. 2 of an alternative embodiment of an intraluminal device having a body, another body and a connector connecting the bodies position at the esophageal-gastric sphincter of the recipient;

[0034] FIG. 4 is a sectional view taken along the lines IV-IV in FIG. 3;

[0035] FIG. 5 is a flattened view of the body in FIG. 3 illustrating interview details thereof;

[0036] FIG. 6 is a side elevation of an alternative embodiment of an intraluminal device adapted to be positioned at the esophageal-gastric sphincter of the recipient;

[0037] FIG. 7 is a sectional view taken along the lines VII-VII in FIG. 6;

[0038] FIG. 8 is a sectional view of the gastro-esophageal region of a patient with an intraluminal device according to an embodiment of the invention deployed therein;

[0039] FIG. 9 is the same view as FIG. 8 showing the lower esophageal sphincter (LES) of the esopho-gastric junction (EGJ) opened to pass a bolus of food;

[0040] FIG. 10 is a perspective view of the intraluminal device in the posture of FIG. 8;

[0041] FIG. 11 is a perspective view of the intraluminal device in the posture of FIG. 9;

[0042] FIG. 12 is a plan view of the mesh supporting structure in FIGS. 8-11 that has been flattened to show details thereof;

[0043] FIG. 13 is the same view as FIG. 8 of an alternative embodiment thereof;

[0044] FIG. 14 is the same view as FIG. 9 of the alternative embodiment in FIG. 13;

[0045] FIG. 15 is a perspective view of the intraluminal device in the posture of FIG. 13;

[0046] FIG. 16 is a perspective view of the intraluminal device in the posture of FIG. 14;

[0047] FIG. 17 is the same view as FIG. 10 of another alternative embodiment thereof;

[0048] FIG. 18 is the same view as FIG. 11 of the another alternative embodiment in FIG. 17;

[0049] FIG. 19 is an enlarged view of an anchor showing details thereof;

[0050] FIG. 20 is the same view as FIG. 19 of an alternative embodiment thereof;

[0051] FIG. 21 is the same view as FIG. 19 of another alternative embodiment thereof;

[0052] FIG. 22 is the same view as FIG. 19 of yet another alternative embodiment thereof; and

[0053] FIG. 23 is the same view as FIG. 19 of an embodiment having multiple tines.

DESCRIPTION OF THE PREFERRED EMBODIMENTS

[0054] The present invention will now be described with reference to the accompanying figures, wherein the numbered elements in the following written description correspond to like-numbered elements in the figures.

[0055] Referring now to the drawings and the illustrative embodiments depicted therein, an intraluminal device 10 is adapted to be deployed in a lumen 12 that experiences peristaltic waves and has muscle defining an intraluminal sphincter or pseudo-sphincter, hereafter “sphincter”. An example of such a lumen is a portion of the gastro-intestinal (GI) tract having sphincters including the upper esophageal sphincter (UES), the esophageal-gastric sphincter (EGS), the pyloric sphincter (PS) and the ileocecal valve (IV) that separates the large intestine from the small intestine. Intraluminal device 10 has a body 14 having a size and shape of a portion of the lumen proximal of the sphincter with respect to peristaltic movement of the lumen and a through opening 15 that allows movement of intraluminal content through the body. The through opening may be a central passage through the body or a shape of the body that allows intraluminal content to bypass the body.

[0056] Intraluminal device 10 further includes at least one tine 16. The at least one tine 16 extends distally from a distal portion of body 14 and is rigid or semi rigid. In this manner, with body 14 deployed in the lumen proximal the sphincter, the at least one tine 16 penetrates the muscle that defines the sphincter as peristalsis causes distal motion of the body thrusting the at least one tine distally. The penetration of the at least one tine in the sphincter is sufficient to resist action of peristalsis of lumen 12 separating the at least one tine from the sphincter. In this manner distal migration of body 14 is resisted even as the sphincter opens and closes. Thus the orientation of the at least one tine penetrating the sphincter resists distal migration of the body without placing excessive sheer force on the at least one tine, while the bulk and thickness of the sphincter resists penetration of the wall of lumen 12 with the tine(s) where intraluminal content could escape outside of the lumen where infection could ensue. This may be accomplished by the angle α between each tine 16 and the central axis of body 14 being between approximately 5 degrees and approximately 45 degrees, such as between approximately 5 degrees and approximately 30 degrees and illustrated as approximately 10 degrees outwardly.

[0057] While one tine 16 may be sufficient to resist distal migration of body 14, at least two tines 16 that are axially spaced around body 14 with respect to lumen 12 enhances and more evenly distributes the forces resisting peristalsis. In the illustrated embodiment, each tine 16 is between approximately 0.5 cm and approximately 2.0 cm. In this manner, even with proximate/distal movement of body 14 in response to peristalsis of lumen 12, any commensurate movement of the tine(s) 16 within the sphincter, will not cause the tine(s) to disengage from the sphincter. If a plurality of tines 16 are used they may be of different lengths to provide a variety of engagements with the sphincter.

[0058] In the illustrated embodiment in FIG. 3, device 10′ body 14′ is coupled with another body 18 with a connector 7. With intraluminal device 10′ deployed at lumen 12 with body 14′ proximal the sphincter and tine(s) 16 penetrating the EG sphincter, another body 18 is distal of the sphincter and connector 7 connecting body 14′ with another body 18 passing through the EG sphincter. Connector 7 is configured to not substantially interfere with operation of the sphincter while passing through the sphincter. FIG. 4 illustrates a possible arrangement of a plurality of tines 16 disposed angularly around the distal end of body 14′. As can be seen, two tines 16 angle radially away from each connector 20 and two tines angle radially away from each other offset from the connectors. Other arrangements are possible.

[0059] Intraluminal device 10′ may be deployed with a deployment device of the type disclosed in commonly assigned U.S. Pat. No. 9,545,326, the disclosure of which is hereby incorporated herein by reference. Deployment begins by compressing body 14′ and another body 18 and positioning them in the deployment device along with connector 7. The deployment device is deployed in the lumen 12 at least partially distal of the EG sphincter using techniques disclosed in the '326 patent. Another body 18 is deployed from the deployment device distal of the EG sphincter. The deployment device is then pulled proximally and body 14′ and at least one tine 16 is deployed from the deployment device in a position that is proximal the muscle of the EG sphincter. After body 14′ is deployed from the deployment device, distal movement of the body will result in the at least one tine 16 penetrating the muscle of the EG sphincter.

[0060] Intraluminal device 10′ may be explanted with an endoscopic grasper or hook pulling proximally on a removal ring 17. In the illustrated embodiment, removal ring 17 is made of a suture or other material weaving between proximal ends of the support mesh of body 14′ (FIG. 5). This distributes the proximal force evenly around the perimeter of body 14′ and pulls the wall inward from the esophagus thus reducing any tendency to injure the esophagus. One or more force transfer sutures 19 transfers the movement of removal ring 17 to a retraction ring 21. Retraction ring 21 retracts tines 16 inwardly in order to reduce any scratching of the tine tips along the esophagus as body 14′ is removed. Retraction ring 21 functions by applying an inward force on a distal end of body 14′, by applying an inward force directly on the tines 16 or by retracting the tines into pockets provided in body 14′. Other methods will be apparent to the skilled artisan.

[0061] For intraluminal device 10′, body 14′ is an esophageal member 11 configured to the size and shape of the distal portion of the esophagus and another body 18 is a cardiac member 13 that is configured to the size and shape of a portion of the cardiac portion of the stomach as illustrated in FIG. 3. Connector 7 passes through the esophageal-gastric (EG) sphincter. Such embodiment is useful as a bariatric device and method as disclosed in commonly assigned international application publication WO 2016/109346 or a metabolic disease treatment device and method as disclosed in commonly assigned international application publication WO 2015/031077 the disclosures of which are hereby incorporated herein by reference. In order to function as a bariatric device or a metabolic disease treatment device, cardiac member 13 applies pressure to the cardiac portion of the stomach at least part of the time via connector 7 being under tension. In order to do so, while allowing esophageal member 11 to be initially deployed sufficiently proximal of the EG sphincter to allow the distal tip of tine(s) 16 to engage the muscle of the EG sphincter, connector 7 and/or cardiac member 13 may be sufficiently flexible in order to accommodate temporary further spacing between the esophageal member and the cardiac member while maintaining position of the cardiac member 13 generally distal of the EG sphincter. This may be accomplished by connector 7 being elastic and/or by cardiac member 13 being flexible. In that manner, the connector and/or cardiac member can flex to allow tine(s) 16 to engage the EG sphincter then relax sufficiently to place pressure on the cardiac portion of the stomach.

[0062] In another embodiment illustrated in FIG. 6 an intraluminal device 410 has a body 414 that is configured to be positioned at a distal portion of the esophagus, another body 418 that is configured to be positioned against the cardiac portion of the stomach and a connector 320 that passes through the esophageal-gastric sphincter in a manner that does not interfere with operation of the EG sphincter. Body 414 is ring-shaped in order to pass intraluminal content through the esophagus and, as can best be seen in FIG. 7, body 414 has a curvilineal cross section in order to minimize any potential irritation of the esophagus.

[0063] Tine(s) 16 can be made of nitinol wire, stainless steel, titanium, carbon fiber, or the like, covered with a biocompatible material such as a silicone coating. This makes the tine(s) stiff yet flexible. Each tine is directed generally distally but with an outward slant. This ensures that the tine engages the sphincter. Each tine is directed more distally than outwardly so that shear forces on the tine are minimal. Also this minimizes possibility of the tine penetrating the wall of lumen 12. For example, the angle between each tine and the central axis of body 314 may be between approximately 5 degrees and approximately 45 degrees but a greater or lesser amount may be used such as between approximately 5 degrees and approximately 30 degrees or approximately 10 degrees. An enlarged tip 26 of tine(s) 16 may be provided to resist catching on a deployment device or other surface. Although two tines 16 are shown, one on each side of body 414, more than two tines may be used. A plurality of additional distally directed tines may be deployed, each between one of the ones shown and body 418.

[0064] An intraluminal device 20 (FIG. 8) is adapted to be deployed in a lumen 22, such as the esophagus that experiences peristaltic waves and has muscle defining an intraluminal sphincter, such as the lower esophageal sphincter (LES) also known as the esophageal gastric sphincter (EGS). Intraluminal device 20 includes a body 24 having a size and shape of a portion of the lumen proximal of the sphincter and one or more anchors 25 extending from body 24 and adapted to resist distal migration of body 24.

[0065] Body 24 includes an esophageal member 30 having a size and shape of a portion of the distal portion of the esophagus and a cardiac member 32 having a size and shape of the cardiac portion of the stomach coupled with esophageal member 30 with a connector 34. Connector 34 in the illustrated embodiment is a pair of tension members, or struts, connecting esophageal member 20 and cardiac member 32, but other configurations are possible. Connector 34 causes cardiac member 32 to apply stress to the cardiac portion of the stomach when connector 32 passes through the EG sphincter. Anchor(s) 25 extend distally from esophageal member 30 resist distal migration of the esophageal member. Each anchor 25 has a base 26 extending distally from esophageal member and one or more tines 27 extending distally from base 26. Each tine may extend directly distally from base 26 or be at a slight angle therefrom. Base 26 positions tine(s) 27 to penetrate the muscle of the esophageal-gastric (EG) sphincter when the esophageal member 30 is deployed in the esophagus upstream of the EG sphincter. Intraluminal device 20 may be deployed in the manner disclosed in International Publication No. WO 2020/194189 A1, the disclosure of which is hereby incorporated herein by reference in its entity, which causes tine(s) 27 of anchor(s) 25 to penetrate the muscle of the EG sphincter.

[0066] Base 26 is sufficiently stiff so as to be resistant to compression but connected with esophageal member 30 in a manner that allows lateral motion of the tine(s) 27 with respect to esophageal member 30 as seen by comparing FIG. 8 with the EGS closed and FIG. 9 with the EGS opened by peristalsis to pass a bolus of food B. In this manner, with tine(s) 27 penetrating the esophageal gastric sphincter (EGS), aka lower esophageal sphincter (LES), the stiffness of base 26 will transmit any force applied to anchor 25 by peristalsis acting on esophageal member 30 to the LES/EGS which will counteract the distal force applied to the esophageal member. Anchor(s) 25 will therefore resist distal migration of esophageal member 30 yet respond to operation of the LES/EGS by passively following changes in the diameter of the LES during peristalsis. This can best be understood by a comparison of FIGS. 8 and 9. In FIG. 8 intraluminal device 20 has been deployed and the LES is closed. FIG. 9 illustrates peristalsis of the esophagus opening the LES in response to a bolus of food B passing from the esophagus to the stomach. This opening of the LES is accommodated by each anchor 25 passively moving laterally along with opening and closing of the LES muscle. This lateral motion of the tine(s) is accomplished by a hinge-like connection 36 between base 26 and the wall of esophageal member 30 which pivotally mounts the base to the esophageal member. However the generally distal orientation of anchor 25 along with the compression resistance of base 26 continues to resist distal migration of intraluminal device 20 while passively following the diameter of the LES during peristalsis.

[0067] As best seen in FIGS. 10-12, esophageal member 30 is generally cylindrical of the diameter of the distal esophagus and defined by a support structure made up of a woven mesh 31 formed of an elongated member 31. In the embodiment illustrated in FIGS. 10-12, mesh 31 includes distal extensions 33 which are woven together with mesh 31 and may be either a separate strand of filament or an extension of the filament that forms mesh 31. Each distal extension 33 is a loop which provides structure to a base 26 with one more tines 27 attached to a distal portion of the extension. Esophageal member 30 additionally includes one or more coatings of a biocompatible material, such as silicone, over mesh 31 and extensions 33. The coatings may be continuous thereby defining a tubular member or may have one or more openings therein. In the illustrated embodiment, the material defining mesh 31 and extensions 33 is a metal such as nitinol which is resistant to compression yet allows lateral flexing without metal fatigue. These characteristics of nitinol provide the functionality of anchors 25, namely resistant to compression yet attached to the esophageal member with a hinge-like connection. Since the biocompatible coating is flexible, it allows the extensions 33 to pivot with respect to mesh 31.

[0068] Esophageal member 30 has a proximal removal ring 40 interwoven with mesh 31. In order to explant esophageal member 30, the physician snares removal ring with a hook-like member and retracts the removal ring. This will result in a decrease in the diameter of mesh 31 and hence the proximal esophageal member to allow the proximal esophageal member to clear the esophagus and be removed proximally. Esophageal member 30 additionally has a distal retraction ring 46 which performs a similar function as removal ring 40 but to the distal portion of the esophageal member and a transfer suture 44 which interconnects removal ring 40 and retraction ring 46. Thus when the physician retracts removal ring 40, the force is transferred by transfer suture 44 to retraction ring 46 which also retracts and shrinks the distal diameter of the esophageal member. This reduction in diameter distally to the esophageal member 30 retracts anchors 25 inwardly away from the esophageal wall so that tines 27 do not score the esophageal wall as the esophageal member is removed.

[0069] In the illustrated embodiment, a plurality of anchors 25 are distributed equally around a perimeter of esophageal member 30. Each tine 27 has a length sufficient to penetrate to the muscularis of the lower esophageal sphincter without penetrating outside of the lumen of the gastrointestinal tract. This penetration is sufficient to prevent the tine from separation from the LES yet avoids potential infections from the microbes in the GI tract entering the abdominal cavity. In the illustrated embodiment, times 27 have a sufficient length to penetrate the muscularis of the LES to further stabilize intraluminal device 20. Tines 27 may have an enlarged diameter 28 in order to resist withdrawal of the tine from the muscle of the LES. With time, tissue of the LES will grow around the enlarged diameter 28 in order assist in resisting withdrawal. As seen best in FIG. 12, the enlarged diameter 28 may be in a distally directed arrowhead shape to allow insertion of the tine in the muscle while resist withdrawal. However other shapes are possible such as a ball-shape in FIG. 20 or double ball shape in FIG. 22. Also a double arrowhead shape of the enlarged diameter may be used as shown in FIG. 21.

[0070] In an alternative embodiment of an intraluminal device 120 shown in FIGS. 13 through 16, anchors 125 are connected with a hinge line connection 136 at a more proximal portion of esophageal member 30. Bases 126 of anchors 125 are longer than bases 26 of anchors 25 in order to position each tine 127 at the LES with intraluminal device 125 deployed. In another alternative embodiment of an intraluminal device 220 shown in FIGS. 17 and 18 anchors 225 are peddle shaped so that as the tines 227 move laterally passively under the opening (FIG. 18) and closing (FIG. 17) action of the LES, the bases 226 or the anchors 225 overlap each other as best seen in FIG. 17. Other embodiments will suggest themselves to the skilled artisan.

[0071] Variations in anchor configuration are shown in FIGS. 20 through 23. In FIG. 20, at least two tines are used that are angular with respect to each other. In FIG. 21 the enlarged diameter of the tine is a multiple arrowhead configuration and in FIG. 22 multiple spheres. In FIG. 23 multiple tines are provide, each supported by a separate strand of the filament defining the mesh.

[0072] Deployment of intraluminal device 20 begins by compressing body 24 and positioning it in a deployment device of the type disclosed in commonly assigned U.S. Pat. No. 9,545,326, the disclosure of which is hereby incorporated herein by reference. The deployment device is deployed in the lumen 22 at least partially distal of the LES using techniques disclosed in the '326 patent. Cardiac member 32 is deployed from the deployment device in the stomach. The deployment device is then pulled proximally to position the cardiac member against the upper portion (cardia) of the stomach and at least partially deploying esophageal member 30 into the esophagus proximal the LES. With further proximal force applied to the deployment device, esophageal member 30 is then fully deployed from the deployment device with the tines 27 proximal of the LES. Distal movement of body 24 from peristalsis will result in the tines 27 penetrating the muscle of the LES as seen in FIG. 8. With tines 27 penetrating the LES, distal migration of intraluminal device 20 will be resisted and normal functioning of the LES will be accommodated as anchors 25 follow the diameter of the LES during operation

[0073] While the foregoing description describes several embodiments of the present invention, it will be understood by those skilled in the art that variations and modifications to these embodiments may be made without departing from the spirit and scope of the invention, as defined in the claims below. The present invention encompasses all combinations of various embodiments or aspects of the invention described herein. It is understood that any and all embodiments of the present invention may be taken in conjunction with any other embodiment to describe additional embodiments of the present invention. Furthermore, any elements of an embodiment may be combined with any and all other elements of any of the embodiments to describe additional embodiments.