US20050075653A1 - Apparatus and methods for forming and securing gastrointestinal tissue folds - Google Patents

Abstract

Apparatus and methods are provided for forming a gastrointestinal tissue fold by engaging tissue at a first tissue contact point and moving the first tissue contact point from a position initially distal to, or in line with, a second tissue contact point to a position proximal of the second contact point, thereby forming the tissue fold, and extending an anchor assembly through the tissue fold from a vicinity of the second tissue contact point. Adjustable anchor assemblies; as well as anchor delivery systems, shape-lockable guides and methods for endoluminally performing medical procedures, such as gastric reduction, treatment of gastroesophageal reflux disease, resection of lesions, and treatment of bleeding sites; are also provided.

Description

CROSS-REFERENCES TO RELATED APPLICATIONS
• The present application is a continuation of U.S. patent application Ser. No. 10/735,030 (Attorney Docket No. 021496-002513US), filed Dec. 12, 2001, which is a Continuation-In-Part of U.S. patent application Ser. No. 10/672,375, filed Sep. 25, 2003, which claims the benefit of the filing date of U.S. provisional patent application Ser. No. 60/500,627, filed Sep. 5, 2003; and is a Continuation-In-Part of U.S. patent applications Ser. No. 10/612,170, filed Jul. 1, 2003, and Ser. No. 10/639,162, filed Aug. 11, 2003; both of which claim the benefit of the filing date of U.S. provisional patent application Ser. No. 60/433,065, filed Dec. 11, 2002. Furthermore, this application is a Continuation-In-Part of U.S. patent application Ser. No. 10/173,203, filed Jun. 13, 2002; as well U.S. patent application Ser. No. 10/458,060, filed Jun. 9, 2003, which is a Continuation-In-Part of U.S. patent application Ser. No. 10/346,709, filed Jan. 15, 2003, and which claims the benefit of the filing date of U.S. provisional patent application Ser. No. 60/471,893, filed May 19, 2003. Furtherstill, this application is a Continuation-In-Part of U.S. patent application Ser. No. 10/288,619, filed Nov. 4, 2002; which is a Continuation-In-Part of U.S. patent application Ser. No. 09/746,579, filed Dec. 20, 2000, and a Continuation-In-Part of co-pending, commonly assigned U.S. patent application Ser. No. 10/188,509, filed Jul. 3, 2002; which is a Continuation-In-Part of U.S. patent application Ser. No. 09/898,726, filed Jul. 3, 2001; which is a Continuation-In-Part of U.S. patent application Ser. No. 09/602,436, filed Jun. 23, 2000, which claims the benefit of the filing date of U.S. provisional patent application Ser. No. 60/141,077, filed Jun. 25, 1999. All of these applications are incorporated herein by reference in their entireties.
BACKGROUND OF THE INVENTIONFIELD OF THE INVENTION
• The present invention relates to methods and apparatus for intraluminally forming and securing gastrointestinal (“GI”) tissue folds. More particularly, the present invention relates to methods and apparatus for reducing the effective cross-sectional area of a gastrointestinal lumen.
• Morbid obesity is a serious medical condition pervasive in the United States and other countries. Its complications include hypertension, diabetes, coronary artery disease, stroke, congestive heart failure, multiple orthopedic problems and pulmonary insufficiency with markedly decreased life expectancy.
• Several surgical techniques have been developed to treat morbid obesity, e.g., bypassing an absorptive surface of the small intestine, or reducing the stomach size. These procedures are difficult to perform in morbidly obese patients because it is often difficult to gain access to the digestive organs. In particular, the layers of fat encountered in morbidly obese patients make difficult direct exposure of the digestive organs with a wound retractor, and standard laparoscopic trocars may be of inadequate length.
• In addition, previously known open surgical procedures may present numerous life-threatening post-operative complications, and may cause atypical diarrhea, electrolytic imbalance, unpredictable weight loss and reflux of nutritious chyme proximal to the site of the anastomosis. Further, the sutures or staples that are often used in these surgical procedures may require extensive training by the clinician to achieve competent use, and may concentrate significant force over a small surface area of the tissue, thereby potentially causing the suture or staple to tear through the tissue.
• The gastrointestinal lumen includes four tissue layers, wherein the mucosa layer is the top tissue layer followed by connective tissue, the muscularis layer and the serosa layer. One problem with conventional gastrointestinal reduction systems is that the anchors (or staples) must engage at least the muscularis tissue layer in order to provide a proper foundation. In other words, the mucosa and connective tissue layers typically are not strong enough to sustain the tensile loads imposed by normal movement of the stomach wall during ingestion and processing of food. In particular, these layers tend to stretch elastically rather than firmly hold the anchors (or staples) in position, and accordingly, the more rigid muscularis and/or serosa layer must be engaged. This problem of capturing the muscularis or serosa layers becomes particularly acute where it is desired to place an anchor or other apparatus transesophageally rather than intraoperatively, since care must be taken in piercing the tough stomach wall not to inadvertently puncture adjacent tissue or organs.
• In view of the aforementioned limitations, it would be desirable to provide methods and apparatus for forming gastrointestinal tissue folds that achieve gastric reduction by reconfiguring the GI lumen of a patient.
• It would be desirable to provide methods and apparatus for forming gastrointestinal tissue folds using anchors that can be reconfigured from a reduced delivery profile to an expanded deployed profile.
• It also would be desirable to provide methods and apparatus for forming gastrointestinal tissue folds, wherein an anchor assembly is extended across stomach folds that include the muscularis and serosa tissue layers.
• It further would be desirable to provide methods and apparatus for forming gastrointestinal tissue folds, wherein the anchor assembly is deployed in a manner that reduces a possibility of injuring neighboring organs.
• It still further would be desirable to provide methods and apparatus for forming gastrointestinal tissue folds, wherein reduced training of a clinician is required to achieve competent use of the anchor assembly.
• It would be desirable to provide methods and apparatus for forming gastrointestinal tissue folds that facilitate approximation of a plurality of tissue folds.
BRIEF SUMMARY OF THE INVENTION
• In view of the foregoing, it is an object of the present invention to provide methods and apparatus for forming gastrointestinal tissue folds that achieve gastric reduction by reconfiguring the GI lumen of a patient.
• It is another object of the present invention to provide methods and apparatus for forming gastrointestinal tissue folds using anchors that can be reconfigured from a reduced delivery profile to an expanded deployed profile.
• It is an additional object of this invention to provide methods and apparatus for forming gastrointestinal tissue folds in which an anchor assembly is extended across stomach folds that include the muscularis and serosa tissue layers.
• It is a further object of the present invention to provide methods and apparatus for forming gastrointestinal tissue folds, wherein the anchor assembly is deployed in a manner that reduces a possibility of injuring neighboring organs.
• It is yet another object to provide methods and apparatus for forming gastrointestinal tissue folds, wherein reduced training of a clinician is required to achieve competent use of the anchor assembly.
• It is an object to provide methods and apparatus for forming gastrointestinal tissue folds that facilitate approximation of a plurality of tissue folds.
• These and other objects of the present invention are accomplished by providing a catheter configured for advancement into a patient's gastrointestinal lumen to form a gastrointestinal tissue fold. In one preferred embodiment, the catheter has a distal region including a tissue grabbing assembly adapted to engage and/or stretch a portion of the tissue wall of the GI lumen at a first tissue contact point. A second tissue contact point is then established with the tissue wall at a location initially proximal of, or in line with, the first tissue contact point. The tissue engaged by the tissue grabbing assembly then is moved to a position proximal of the second tissue contact point to form a tissue fold, and one or more anchor assemblies may be delivered across the tissue fold. Preferably, delivery of the anchor assembly across the tissue fold includes delivering the anchor assembly across the muscularis and serosa layers of the tissue wall.
• Optionally, a third tissue contact point may be established at another location initially proximal of, or in line with, the first tissue contact point. Upon movement of the tissue engaged by the tissue grabbing assembly to a position proximal of both the second and third tissue contact points, a tissue fold is formed with the second and third contact points on opposing sides of the fold. The third contact point may provide backside stabilization upon delivery of the anchor assembly across the tissue fold from a vicinity of the second tissue contact point.
• In a preferred embodiment, the tissue grabbing assembly is carried on a first flexible tube associated with the distal region of the catheter, and the one or more anchor assemblies are delivered by an anchor delivery system disposed within a second flexible tube associated with the distal region of the catheter. The tissue grabbing assembly may comprise any of a number of mechanisms configured to engage the tissue wall, including a pair of jaws configured to move between open and closed positions, a plurality of linearly translating barbs, a coil screw, or one or more needles or hooks. The first tissue contact point may be moved from a tissue engagement position distal to, or in line with, the second tissue contact point, to the tissue folding position by any of a number of mechanisms, including a hinge assembly, a treadmill assembly, or a linear pull assembly.
• More preferably, the distal region of the catheter includes a bendable section that permits the first tissue contact point to be positioned relative to the second tissue contact point so that the tissue fold is oriented substantially perpendicular to the anchor delivery system. In this manner, the anchor delivery system, when deployed, pierces the tissue fold and exits into the interior of the GI lumen, rather than the exterior of the tissue wall, thereby reducing a risk of injury to adjacent organs.
• The anchor assembly delivery system of the present invention preferably comprises a needle or obturator adapted to pierce the tissue fold and deliver an anchor assembly. In one preferred embodiment, the anchor assembly comprises a pair of rod-like anchors that are delivered through a needle in a reduced delivery profile, wherein the longitudinal axis of the rods is substantially parallel to the longitudinal axis of the needle. Once ejected from the needle, the rods rotate about 90 degrees to engage the tissue. In other embodiments, the anchor assembly may comprise anchors of various shapes delivered, for example, over the exterior of an obturator.
• In a preferred embodiment of the present invention, the catheter is adapted to form a plurality of gastrointestinal tissue folds that may be approximated. Optionally, an anchor assembly may be placed across each tissue fold, and the plurality of tissue folds then may be approximated by cinching the plurality of anchor assemblies together. Alternatively, an anchor assembly may be placed across a plurality of tissue folds, and the plurality of tissue folds may be approximated by cinching the anchor assembly. As yet another alternative, a plurality of tissue folds may be approximated prior to placement of an anchor assembly. One or more anchor assemblies then may be placed across the approximated plurality of tissue folds to secure the plurality in the approximated position. Multiple pluralities of tissue folds may be joined together and/or approximated in order to perform a procedure, for example, a gastric reduction or treatment of gastroesophageal reflux disease (“GERD”).
• To facilitate proper positioning, as well as visualization, of the tools and instruments of the present invention at a treatment site within a tortuous lumen or within unpredictably supported anatomy, a shape-lockable guide may be provided having a flexible state and reversibly rigidizable state. This guide may comprise an overtube through which instruments of the present invention, as well as an endoscope, may be advanced. As described hereinafter, exemplary procedures achievable when using tools of the present invention in conjunction with an endoscope include, for example, endoluminal gastric reduction and endoluminal treatment of GERD.
• Methods of using the apparatus of the present invention also are provided.
BRIEF DESCRIPTION OF THE DRAWINGS
• The above and other objects and advantages of the present invention will be apparent upon consideration of the following detailed description, taken in on junction with the accompanying drawings, in which like reference characters refer to like parts throughout, and in which:
• FIGS. IA and1B are, respectively, a side view and detail view of apparatus of the present invention for forming a gastrointestinal fold in accordance with the principles of the present invention.
• FIGS. 2A and 2B are side-sectional views of a tissue grabbing assembly suitable for use with the apparatus ofFIG. 1.
• FIGS. 3A-3E are side views illustrating a method of using the apparatus ofFIG. 1 to form a gastrointestinal fold.
• FIGS. 4A-4C are side-sectional views of an anchor assembly and delivery system suitable for use with apparatus of the present invention.
• FIGS. 5A and 5B are side-sectional views of another anchor assembly suitable for use with apparatus of the present invention.
• FIGS. 6A and 6B are side-sectional views of another alternative anchor assembly suitable for use with apparatus of the present invention.
• FIGS. 7A-7C are, respectively, a schematic side-sectional view of a unidirectionally adjustable anchor assembly suitable for use with apparatus of the present invention, schematic side-sectional views of alternative techniques for fixing the distal anchor of the assembly, and a cross-sectional view of the proximal anchor taken along section line A-A ofFIG. 7A.
• FIGS. 8A and 8B are schematic cross-sectional views illustrating the unidirectional adjustment capability of the anchor assembly ofFIG. 7.
• FIGS. 9A-9C are schematic cross-sectional views of alternative embodiments of the proximal anchor of the anchor assembly ofFIG. 7.
• FIGS. 10A and 10B are schematic cross-sectional views of an alternative unidirectionally adjustable anchor assembly suitable for use with apparatus of the present invention.
• FIGS. 11A-11C are, respectively, a schematic side-view of another alternative unidirectionally adjustable anchor assembly suitable for use with the present invention, and cross-sectional views of the same taken along section line B-B ofFIG. 11A.
• FIG. 12 is a schematic cross-sectional view of an alternative unidirectionally adjustable anchor assembly comprising pivoting paddles.
• FIG. 13 is a schematic cross-sectional view of an alternative unidirectionally adjustable anchor assembly comprising spring material.
• FIGS. 14A-14B are schematic side-sectional views or alternative unidirectionally adjustable anchor assemblies comprising one-way valves.
• FIGS. 15A-15C are side-sectional and detail views of alternative unidirectionally adjustable anchor assemblies comprising slipknots.
• FIGS. 16A-16C are, respectively, a schematic side-sectional view of a bi-directionally adjustable anchor assembly comprising a locking mechanism, and cross-sectional views of the same taken along section line C-C ofFIG. 16A.
• FIGS. 17A-17D are perspective views of alternative anchors suitable for use with the anchor assemblies of the present invention.
• FIGS. 18A-18D are side views of alternative apparatus for forming a gastrointestinal fold.
• FIG. 19 is a cross-sectional view of the apparatus ofFIGS. 18A-18D.
• FIGS. 20A-20D are side views of further alternative apparatus for forming a gastrointestinal tissue fold in accordance with the principles of the present invention.
• FIGS. 21A-21G are schematic side-sectional views of an anchor delivery system adapted for use with the adjustable anchor assemblies ofFIGS. 7-17, illustrating a method of delivering the unidirectionally adjustable anchor assembly ofFIG. 7 across a tissue fold.
• FIGS. 22A and 22B are, respectively, a schematic side-view, partially in section, and an end-view of an alternative anchor delivery system adapted for use with the adjustable anchor assemblies ofFIGS. 7-17, wherein the proximal anchor is disposed within a separate delivery tube.
• FIG. 23 is a schematic side-sectional view of an alternative anchor delivery system adapted for use with the adjustable anchor assemblies ofFIGS. 7-17, wherein both the proximal and distal anchors are loaded within the needle.
• FIG. 24 is a schematic side-sectional view of an alternative embodiment of the anchor delivery system ofFIG. 23 comprising motion limitation apparatus.
• FIG. 25 is a schematic side view, partially in section of an alternative anchor delivery system adapted to deliver a plurality of anchor assemblies.
• FIG. 26 is a schematic side view of an alternative embodiment of the anchor delivery system ofFIG. 25.
• FIGS. 27A and 27B are, respectively, schematic isometric and side views, partially in section, of an alternative anchor delivery system adapted to deliver a plurality of anchor assemblies via a revolver.
• FIGS. 28A and 28B are side views of an alternative embodiment of the apparatus ofFIG. 20 illustrating a method for simultaneously forming and approximating multiple gastrointestinal tissue folds.
• FIG. 29 is an isometric view of an alternative embodiment of the apparatus ofFIG. 1 for forming a gastrointestinal tissue fold comprising backside stabilization.
• FIGS. 30A-30E are a side view, partially in section, and isometric views illustrating a method of using the apparatus ofFIG. 29 to form a backside stabilized gastrointestinal tissue fold.
• FIGS. 31A-31C are side views of further alternative tissue folding apparatus illustrating a method for forming a gastrointestinal tissue fold via a linear displacement of tissue.
• FIG. 32 is a side view of an alternative embodiment of the apparatus ofFIG. 31 providing enhanced flexibility.
• FIGS. 33A and 33B are side views of further alternative front and backside stabilized linear displacement plication apparatus, illustrating a method for forming a gastrointestinal tissue fold.
• FIGS. 34A and 34B are, respectively, a side view and a side view, partially in section, of still further alternative apparatus illustrating a method for forming a stabilized gastrointestinal tissue fold via a braided mesh.
• FIG. 35 is a side view of illustrative shape-lockable apparatus for use with the tissue folding and anchor delivery apparatus of the present invention.
• FIG. 36 is a side-sectional exploded view of nestable elements of a first embodiment of an overtube suitable for use with the shape-lockable apparatus ofFIG. 35.
• FIG. 37 is a side-sectional view of a distal region of the apparatus ofFIG. 35 constructed in accordance with principles of the present invention.
• FIG. 38 is a side-sectional view of an illustrative arrangement of a mechanism suitable for use in the handle of the apparatus ofFIG. 35.
• FIG. 39 is a side-sectional view of the detail of a wire clamping system suitable for use in the handle ofFIG. 35.
• FIGS. 40A-40D are side-views, partially in section, illustrating an exemplary method of performing endoluminal gastric reduction with a system of tools illustratively comprising the shape-lockable apparatus ofFIGS. 35-39, the plication apparatus ofFIGS. 1-3, the anchor assembly ofFIG. 7, the anchor delivery system ofFIG. 21 and a commercially available gastroscope.
• FIGS. 41A-41C are, respectively, an isometric view of a patient's stomach after performing endoluminal gastric reduction using the methods ofFIG. 40; a cross-sectional view of the same along plane A-A inFIG. 41A; and a cross-sectional view of the stomach along plane B-B inFIG. 41A, prior to approximation of the pluralities of tissue folds to achieve the gastric reduction.
• FIGS. 42A-42C are side-views, partially in section, illustrating an exemplary method of treating gastroesophageal reflux disease with the illustrative system of tools described with respect toFIG. 40.
• FIGS. 43A and 43B are side-views, partially in section, illustrating an alternative method of performing endoluminal gastric reduction utilizing a system of tools of the present invention.
• FIG. 44 is a side view, partially in section, illustrating a method of resecting a lesion or early cancer utilizing a system of tools of the present invention illustratively comprising a suction applicator and a resection loop.
• FIG. 45 is a side view, partially in section, illustrating a method of treating a bleeding site utilizing a system of tools of the present invention.
DETAILED DESCRIPTION OF THE INVENTION
• In accordance with the principles of the present invention, methods and apparatus are provided for intraluminally forming and securing gastrointestinal (“GI”) tissue folds, for example, to reduce the effective cross-sectional area of a GI lumen. These methods and apparatus may be used to treat obesity by approximating the walls of a gastrointestinal lumen to narrow the lumen, thus reducing the area for absorption in the stomach or intestines. More particularly, the present invention involves endoscopic apparatus that engages a tissue wall of the gastrointestinal lumen, creates one or more tissue folds and disposes one or more anchor assemblies through the tissue fold(s). Preferably, the anchor assemblies are disposed through the muscularis and/or serosa layers of the gastrointestinal lumen. In operation, a distal tip of the probe engages the tissue and then moves the engaged tissue to a proximal position relative to the catheter tip, thereby providing a substantially uniform plication of predetermined size.
• Formation of a tissue fold preferably is accomplished using at least two tissue contact points that are separated by a linear or curvilinear distance, wherein the separation distance between the tissue contact points affects the length and/or depth of the fold. In operation, a tissue grabbing assembly engages the tissue wall in its normal state (i.e., non-folded and substantially flat), thus providing a first tissue contact point. The first tissue contact point then is moved to a position proximal of a second tissue contact point to form the tissue fold. An anchor assembly then may be extended across the tissue fold at the second tissue contact point. Optionally, a third tissue contact point may be established such that, upon formation of the tissue fold, the second and third tissue contact points are disposed on opposing sides of the tissue fold, thereby providing backside stabilization during extension of the anchor assembly across the tissue fold from the second tissue contact point.
• Preferably, the first tissue contact point is used to engage and then stretch or rotate the tissue wall over the second tissue contact point to form the tissue fold. The tissue fold is then articulated to a position wherein a portion of the tissue fold overlies the second tissue contact point at an orientation that is substantially normal to the tissue fold. An anchor then is delivered across the tissue fold at or near the second tissue contact point.
• Referring toFIG. 1,apparatus10 of the present invention comprisestorqueable catheter11 havingdistal region12 from which first and second interconnectedflexible tubes13 and14 extend, andproximal region15 havinghandle16 andactuator17.Catheter11 is configured for insertion through a patient's mouth and esophagus into the gastrointestinal lumen.Tissue grabbing assembly18 is disposed on the distal end offlexible tube13, and is coupled toactuator17 viacontrol wire19 that extends throughflexible tube13.
• As better illustrated inFIG. 1B,flexible tubes13 and14 are connected viahinge assembly20 that compriseslink21 attached toflexible tube13 atpivot point22 and attached toflexible tube14 atpivot point23.Hinge assembly20 preventstissue grabbing assembly18 from moving more than a predetermined distance relative todistal end24 offlexible tube14.
• Still referring toFIG. 1B,flexible tubes13 and14 preferably includebendable sections25 and26, respectively. The bendable sections may comprise, for example, a plurality of through-wall slots27 to enhance flexibility of the tube. Preferably,flexible tubes13 and14 are made from stainless steel with an etched or laser-cut slot pattern. More preferably, the slot pattern is a sinusoidal repeating pattern of slots perpendicular to the longitudinal axis oftubes13 and14. Alternative flexible patterns will be apparent to those of skill in the art.
• Referring toFIGS. 2A and 2B,tissue grabbing assembly18 comprises pair ofjaws28a,28barranged to rotate aboutpivot point29 between an open configuration (FIG. 2A) and a closed configuration (FIG. 2B).Control wire19 is coupled viapivot point30 toarms31aand31b.Arms31aand31bare in turn pivotally coupled tojaws28aand28b,respectively, at pivot points32aand32b.Each ofjaws28aand28bpreferably includes sharpenedteeth33 disposed near its distal ends to facilitate grasping of the tissue wall of the GI lumen.
• Control wire19 is coupled toactuator17 ofhandle16 so that translation of the wire withinflexible tube13 causes the jaws to open or close. In particular, urging control wire distally (as indicated by arrow A inFIG. 2A) movespivot point30 distally, thereby forcing the jaws to open. Urgingcontrol wire19 proximally (as indicated by arrow B inFIG. 2B) movespivot point30 proximally, thereby forcing the jaws to close together. In alternative embodiments,tissue grabbing assembly18 may comprise a grappling hook or fork, or plurality of needles coupled to the distal end offlexible tube13.
• Flexible tube14 is affixed to and immovable withincatheter11, whileflexible tube13 is coupled tocatheter11 only viahinge20. Accordingly, whencontrol wire19 is extended in the distal direction,flexible tube13 is carried in the distal direction. Whencontrol wire19 is retracted in the proximal direction, flexible tube remains stationary untiljaws28aand28bclose together, after which further retraction ofcontrol wire19 by movingactuator17 causesflexible tube13 to buckle inbendable region25, as described hereinafter.
• Referring now toFIGS. 1 and 3A-3E, operation ofapparatus10 is described to create a tissue fold in a tissue wall of a GI lumen. InFIG. 3A,distal region12 ofcatheter11 is positioned within a patient's GI lumen transesophageally, andjaws28aand28boftissue grabbing assembly18 are opened by movingactuator17 to the distal-most position onhandle16. As depicted inFIG. 3B,actuator17 may then be moved proximally until the jaws oftissue grabbing assembly18 engage a portion of tissue wall W at contact point P1.
• Referring toFIG. 3C, after the tissue wall has been engaged at contact point P1,flexible tube13 is urged proximally withincatheter11 by further proximal retraction ofcontrol wire19 to stretch tissue wall W and create tissue fold F. During this movement offlexible tube13, link21 ofhinge assembly20 causestissue grabbing assembly18 to move from a position distal todistal end24 offlexible tube14, to a position proximal ofdistal end24 offlexible tube14.Bendable sections25 and26 offlexible tubes13 and14, respectively, accommodate any lateral motion caused by operation ofhinge assembly20. Advantageously, formation of fold F facilitates the penetration of the tissue wall by a needle and subsequent delivery of an anchor assembly, as described hereinafter.
• Referring toFIG. 3D, additional proximal movement ofactuator17 causesflexible tubes13 and14 to buckle atbendable sections25 and26.Hinge assembly20 transmits force applied toflexible tube13 viacontrol wire19 andactuator17 to thedistal tip24. Preferably,flexible tube14 is configured so thatdistal tip24 contacts, and is substantially perpendicular, to tissue fold F at contact point P2. As illustrated inFIG. 3E, once tissue fold F is stretched acrossdistal tip24 offlexible tube14, sharpened needle orobturator34 may be extended fromdistal tip24 offlexible tube14 to pierce all four layers of the tissue wall W. Sharpened needle orobturator34 is inserted viainlet35 toflexible tube14 on handle16 (see FIG. IA).
• As discussed above, the GI lumen comprises an inner mucosal layer, connective tissue, the muscularis layer and the serosa layer. To obtain a durable purchase, e.g., in performing a stomach reduction procedure, the staples or anchors used to achieve reduction of the GI lumen must engage at least the muscularis tissue layer, and more preferably, the serosa layer as well. Advantageously, stretching of tissue fold F acrossdistal tip24 permits an anchor to be ejected through both the muscularis and serosa layers, thus enabling durable gastrointestinal tissue approximation.
• As depicted inFIG. 3E, after tissue fold F is stretched acrossdistal tip24 offlexible tube14 to form contact point P2 with tissue wall W,needle34 may be extended fromdistal tip24 and through tissue fold F. Becauseneedle34 penetrates the tissue wall twice, it exits within the gastrointestinal lumen, thus reducing the potential for injury to surrounding organs. Once the needle has penetrated tissue fold F, an anchor assembly is ejected throughdistal tip24 as described hereinbelow.
• With respect toFIGS. 4A-4C, a first embodiment of an anchor assembly suitable for use with the apparatus of the present invention is described.Anchor assembly36 comprises T-anchor assembly havingdistal rod38aandproximal rod38bconnected bysuture39. The precise shape, size and materials of the anchors may vary for individual applications. In addition, the suture material also may vary for individual applications. By way of example, the suture material may consist of monofilament wire, multifilament wire or any other conventional suture material. Alternatively,suture39 may comprise elastic material, e.g. a rubber band, to facilitate adjustment of the distance between the proximal and distal rods.Suture39 extends through a pair of through-holes40 in each rod, thereby forming a loop. Alternatively,suture39 may be attached to the rods via an eyelet or using a suitable adhesive. Preferably, through-holes40 are located near the center of therods38aand38b.
• Referring toFIG. 4B,rods38aand38bmay be delivered through needle34 (seeFIG. 3E) usingpush rod42. Pushrod42 is adapted to freely translate throughflexible tube14 andneedle34. Pushrod42 is referably flexible, so that it may slide throughendable section26 offlexible tube14. In addition,push rod42 may includenotch43 near its distal end to facilitate grasping and tensioningsuture39 after anchor delivery.
• During anchor delivery, the longitudinal axis ofdistal rod38ais substantially parallel to the longitudinal axis ofneedle34. However, oncedistal rod38ais ejected fromneedle34, suture tension induces the rod to rotate approximately 90 degrees about its longitudinal axis, so that its longitudinal axis is substantially perpendicular to the longitudinal axis ofneedle35. This rotation ofdistal rod38aprevents it from being pulled back through tissue wall W.
• Referring toFIG. 4C, oncerod38ais ejected on the distal side of fold F,needle35 is retracted and pushrod42 is used to ejectrod38bon the proximal side of tissue fold F. Likedistal rod38a,tension in the suture causesproximal rod38bto rotate about 90 degrees once it is ejected from the needle.Notch43 inpush rod42 then may be employed to tightensuture39 by any of a variety of mechanisms. Alternatively,suture39 may comprise an elastic material that dynamically tightens the rods against tissue fold F.
• Referring now toFIG. 5A, according to other embodiments, the anchor assembly comprises a T-anchor assembly suitable to be disposed overobturator50. More particularly,distal rod38aincludes through-hole51 dimensioned for the passage ofobturator tip52, andobturator50 is translatably inserted throughflexible tube14 viainlet35 of handle16 (see FIG. IA).Proximal rod38bmay be a solid rod that does not include a through-hole for passage ofobturator50. Alternatively,proximal rod38bmay include a through-hole for the passage of the obturator. Preferably,abturator tip52 is sharpened to facilitate tissue penetration.
• With respect toFIG. 5B, oncerod38ais ejected on the distal side of fold F, it rotates into a position substantially parallel to tissue wall W and perpendicular to the longitudinal axis of the obturator.Obturator50 then is retracted andproximal rod38bis ejected fromflexible tube14. More particularly, whenflexible tube14 is retracted from tissue wall W,proximal rod38bis pulled throughdistal tip24.Proximal rod38bthen rotates substantially 90 degrees as it is ejected fromflexible tube14 so thatrod38bis urged against tissue wall W.
• Referring toFIG. 6A, according to further embodiments,anchor assembly55 comprises a T-anchor assembly similar to the embodiment depicted inFIG. 4A. However,anchor assembly55 includesfine wire tether56 that may be twisted to maintain the tension betweenrods38aand38b.
• With respect toFIG. 6B, a method of deliveringanchor assembly55 is described. Initially,distal rod38ais delivered across both tissuewalls using needle34. The needle then is retracted to releasedistal rod38aso that it engages the tissue wall. Next,needle34 is retracted to releaseproximal rod38b,so that it too rotates into engagement with the tissue wall. A proximal portion of the wire tether is captured bynotch43 of push rod42 (seeFIG. 4B), and the push rod is rotated to causeproximal rod38bto clamp down on the tissue fold. Becausewire tether56 is twisted by rotation ofpush rod42, it maintains the desired force on the tissue walls.
• Referring now toFIG. 7, a unidirectionally adjustable anchor assembly suitable for use with apparatus of the present invention is described.Anchor assembly60 comprisesdistal anchor62 and unidirectionally adjustableproximal anchor64, which are connected bysuture39.Distal anchor62 is translationally fixed with respect tosuture39. Such fixation may be achieved in a variety of ways. For example, as seen inFIG. 7A,distal anchor62 may comprise a pair of through-holes63, located near the center ofanchor62 and through which suture39 is threaded and tied off atknot65.
• FIG. 7B provides alternative techniques for fixing the distal anchor. As seen inFIG. 7B(i),distal anchor62 may comprise hollow tube T having opening O. A distal end ofsuture39 is passed throughopening0 and formed into knot K, which is dimensioned such that it cannot pass throughopening0, thereby fixing the distal anchor with respect to the suture. In order to facilitate formation of knot K,distal anchor62 optionally may comprise distal opening DO, which is dimensioned such that knot K may pass therethrough. The distal end ofsuture39 may be passed through distal opening DO, knotted, and then pulled back within hollow tube T ofanchor62 until it catches at opening O.
• A drawback of the fixation technique described with respect toFIG. 7B(i) is a risk ofsuture39 being torn or cut due to rubbing againstopening0. InFIG. 7B(ii), hollow tube T comprises first end E to which is connected wire loop L, which may be formed, for example from a nickel-titanium alloy (“Nitinol”).Suture39 passes through the wire loop before terminating at knot K. Knot K is dimensioned such that it cannot pass back through the wire loop. Wire loop L directssuture39 throughopening0, thereby reducing rubbing of the suture against the opening and reducing a risk of tearing or cutting ofsuture39.
• FIG. 7B(iii) provides yet another alternative technique for fixing the distal anchor with respect to the suture.Distal anchor62 again comprises hollow tube T having opening O. Rod R is disposed within tube T, and the ends of the tube may be either closed or crimped to rod R, such that the rod is maintained within the tube. The distal end ofsuture39 is threaded throughopening0, around rod R, and back out opening O. The suture is then knotted at knot K, thereby fixingdistal anchor62 with respect tosuture39.
• In addition to the techniques shown inFIGS. 7A and 7B,suture39 alternatively may be fixed with respect to anchor62 by other means, for example, via a knotted eyelet or via a suitable adhesive. Additional techniques will be apparent to those of skill in the art. Whileanchor62 is illustratively shown as a rod- or T-type anchor, any of a variety of anchors, per se known, may be used asdistal anchor62. Exemplary anchors are described in co-pending U.S. patent application Ser. No. 10/612,170, filed Jul. 1, 2003, which is incorporated herein by reference in its entirety. Additional anchors are described hereinbelow with respect toFIGS. 17. For the purposes of the present invention, anchors and anchor assemblies should be understood to include clips for securing tissue, as well as suture knots and knot replacements. Furthermore, anchor assemblies may comprise multiple components that are not initially coupled to one another; the components may be brought together and/or coupled within a patient at a treatment site.
• Referring again toFIG. 7A, adjustableproximal anchor64 comprisesouter cylinder66 having first end67aandsecond end67b,as well asfirst opening68aandsecond opening68b.First and second openings68 are preferably disposed near the center ofcylinder66 and approximately 180° apart.Anchor64 further comprises firstflexible rod70aand secondflexible rod70b,both of which are disposed withinouter cylinder66 and coupled to first and second ends67 ofcylinder66. Rods70 may be formed, for example, from Nitinol or from a polymer, and may be separated from one another by small gap G. As with the previous anchor assemblies, the precise shape, size and materials of the anchors and suture may vary as required for specific applications.
• As best seen inFIG. 7C,suture39 passes fromdistal anchor62 throughfirst opening68aofproximal anchor64, around secondflexible rod70b,around firstflexible rod70a,betweenrods70aand70b,and out throughsecond opening68b.This suture winding provides a unidirectional adjustment capability that allows a length L ofsuture39 disposed betweendistal anchor62 andproximal anchor64 to be shortened. However, the suture winding precludes an increase in length L.FIG. 8 illustrate the mechanism of this unidirectional adjustment capability in greater detail. Optionally,suture39 may be tied off proximal ofanchor64 atknot69, thereby forming a proximal loop of suture to facilitate deployment and/or adjustment ofanchor assembly60.
• InFIG. 8A, a proximally-directed force F₁is applied to suture39 proximal ofadjustable anchor64, whileanchor64 is held stationary or is advanced distally. A portion of force F₁is transferred throughsuture39 to secondflexible rod70b,which causesrod70bto bow, thereby increasing gap G and allowingsuture39 to freely pass betweenrods70aand70band throughproximal anchor64, facilitating unidirectional adjustment. Whenanchor64 is held stationary whilesuture39 is retracted proximally,distal anchor62 retracts proximally towardsanchor64. Alternatively, whenanchor64 is advanced distally whilesuture39 is retracted proximally,distal anchor62 either remains stationary or retracts proximally towardsproximal anchor64, depending upon a degree of distal advancement ofproximal anchor64. Regardless, length L ofsuture39 disposed betweenanchors62 and64 is decreased, thereby unidirectionally adjusting a distance between the anchors.
• InFIG. 8B, a distally-directed force F₂is applied to suture39 distal ofadjustable anchor64. Force F₂may be applied, for example, by tissue compressed betweenanchors62 and64. Compressed tissue stores energy in a manner similar to a compression spring and seeks to pushanchors62 and64 apart after unidirectional tightening. Force F₂causes the loop ofsuture39 around first and second rods70 to tighten, thereby bowing both rods inward and closing gap G such thatsuture39 is friction locked between first and second flexible rods70. In this manner, the length L of suture betweenanchors62 and64 may be selectively decreased but cannot be increased.
• As will be apparent to those of skill in the art, the magnitude of force required to unidirectionally adjust length L may be altered in a variety of ways. For example, a length, flexibility or diameter of rods70 may be altered. Likewise, the elasticity or diameter ofsuture39 may be altered. Initial gap G may be increased or decreased. Furtherstill, the materials used to form rods70 andsuture39 may be changed to alter material properties, such as coefficients of friction, and/or rods70 orsuture39 may comprise a lubricious coating. Additional methods for varying the magnitude of force, a few of which are described hereinbelow with respect toFIG. 9, will be apparent in view of this disclosure and are included in the present invention. Referring now toFIG. 9, alternative anchors64 are described. InFIG. 9A, flexible rods70 of proximaladjustable anchor64′ are rotated with respect to openings68 (or vice versa). When utilizing the suture winding described inFIGS. 7 and 8, rotation of rods70 up to 180° clockwise progressively increases friction when force is applied toanchors62 and64. The magnitude of the friction lock is increased when force is applied in the manner described with respect toFIG. 8B. However, friction is also increased when unidirectionally adjusting the length of suture between the proximal and distal anchors by applying force in the manner described with respect toFIG. 8A. Rotation of rods70 more than about 180° clockwise would causeanchor64′ to friction lock regardless of which direction force were applied tosuture39, thereby negating the unidirectional adjustment capability. Counterclockwise rotation of rods70 with respect to openings68 would initially reduce friction during force application to suture39 in either direction. It is expected that counterclockwise rotation in excess of about 90° would eliminate the friction lock described inFIG. 8B and allow bidirectional adjustment. Continued counterclockwise rotation beyond about 450° would reverse the directions of friction lock and unidirectional adjustment, while counterclockwise rotation beyond about 720° would result in friction lock regardless of which direction force were applied tosuture39.
• As discussed previously, openings68 ofcylinder66 ofanchor64 are preferably disposed approximately 180° apart from one another. However, in order to increase the friction lock force without significantly increasing friction during unidirectional adjustment,first opening68amay be rotated counterclockwise with respect tosecond opening68b(or vice versa), as seen withanchor64″ ofFIG. 9B. In this manner,first opening68ais no longer in line with rods70, whilesecond opening68bremains in line with rods70. When force F₁is applied to anchor64″, secondflexible rod70bis able to bow outward and increase gap G, thereby facilitating unidirectional adjustment. Likewise, when force F₂is applied to the anchor, gap G is closed more tightly uponsuture39, thereby increasing the friction lock force. Iffirst opening68aalternatively were rotated clockwise with respect to the second opening, it is expected that the friction lock force would be decreased.
• InFIG. 9C, proximaladjustable anchor64′″ comprises an alternative suture winding.Suture39 passes fromdistal anchor62 throughfirst opening68aofanchor64′″, around secondflexible rod70b,around firstflexible rod70a,back around secondflexible rod70b,betweenrods70aand70b.,and out throughsecond opening68b.As with the suture winding described with respect to anchor64 ofFIGS. 7 and 8, the suture winding illustrated inFIG. 9C provides a unidirectional adjustment capability that allows a length L ofsuture39 disposed betweendistal anchor62 andproximal anchor64′″ to be shortened. However, this suture winding precludes an increase in length L. Additional unidirectionally adjustable suture windings will be apparent to those of skill in the art.
• With reference toFIG. 10, an alternative unidirectionally adjustable anchor comprising three rods is described.Anchor assembly80 comprisesdistal anchor62 andproximal anchor82. Unidirectionally adjustableproximal anchor82 comprisesouter cylinder84 having first end85aand second end85b(not shown), as well asfirst opening86aandsecond opening86b.First and second openings86 are preferably disposed near the center ofcylinder84 and approximately 1800 apart.Anchor82 further comprises firstflexible rod88a,secondflexible rod88band thirdflexible rod88c,all of which are disposed withinouter cylinder66 and coupled to first and second ends85 ofcylinder64. Rods88 are separated from one another by gaps G1 and G2.
• Suture39 passes fromdistal anchor62 throughfirst opening86aofproximal anchor82, aroundfirst rod88a,betweenfirst rod88aandsecond rod88b,betweensecond rod88bandthird rod88c,aroundthird rod88c,back to and aroundfirst rod88a,and out throughsecond opening86b.As seen inFIG. 10A, when force F₁is applied to suture39, gaps G and G2 remain open, thereby facilitating unidirectional adjustment/shortening of length L ofsuture39 disposed betweendistal anchor62 andproximal anchor82. As seen inFIG. 10B, when force F₂is applied to suture39, gaps G1 and G2 close down uponsuture39, thereby forming a friction lock that precludes an increase in length L ofsuture39.
• Referring now toFIG. 11, an alternative three rod anchor assembly is described. The unidirectionally adjustable anchors described hereinabove with respect toFIGS. 7-10 all comprise rods disposed within a cylinder having openings for passage of a suture. The openings act to center the suture with respect to the rods and can be used to alter magnitudes of force applied during adjustment and friction locking, as discussed previously. However, such openings present a risk of tearing or cutting the suture as the suture slides through the openings.
• As seen inFIG. 11,anchor assembly90 comprisesdistal anchor62 andproximal anchor92. Unidirectionally adjustableproximal anchor92 comprises firstflexible rod94aand secondflexible rod94b,as well asrigid rod96, which is preferably larger in diameter than first and second rods94. Flexible rods94 are preferably fabricated from Nitinol or a polymer, whilerigid rod96 is preferably fabricated from stainless steel or a polymer. Alternative materials will be apparent to those of skill in the art.
• Anchor92 further comprises firstouter cylinder98aand secondouter cylinder98b,which are crimped to the ends of first and second rods94, andrigid rod96. As an alternative to crimping, first and second cylinders98 may each comprise an end cap (not shown) to which the rods are coupled. First and second cylinders94 do not span a central portion ofanchor92. Flexible rods94 are separated from one another by gap G1, while rods94 are separated fromrigid rod96 by gap G2.
• Anchor92 comprises three rods, but, unlikeanchor82 ofFIG. 10,suture39 is only wrapped around two of them to achieve unidirectional adjustment. As best seen inFIGS. 11B and 11C, the illustrative suture winding ofanchor assembly90 is similar to that described previously with respect to anchorassembly60 ofFIGS. 7 and 8. The break between first and second cylinders98 acts to centersuture39 with respect to the rods, as seen inFIG. 11A, whilerigid rod96 acts to stiffen and reduce rotation ofanchor92 as it directssuture39 about flexible rods94.
• Suture39 passes fromdistal anchor62 toproximal anchor92, betweenrigid rod96 and flexible rods94, around secondflexible rod94b,around firstflexible rod94a,betweenrigid rod96 and firstflexible rod94a,betweenflexible rods94aand94b,and out. As seen inFIG. 11A, when force F₁is applied to suture39, flexible rods94 are forced apart and gap G1 widens while gap G2 remains substantially constant, thereby allowing unidirectional adjustment of length L ofsuture39 disposed betweendistal anchor62 andproximal anchor92. As seen inFIG. 11B, when force F₂is applied to suture39, gap G1 closes down uponsuture39, thereby forming a friction lock that precludes an increase in length L ofsuture39. Gap G2 again remains substantially constant.
• With reference toFIG. 12, an alternative unidirectionally adjustable anchor assembly comprising pivots is described.Anchor assembly100 comprisesdistal anchor62 and proximal anchor102. Unidirectionally adjustable proximal anchor102 comprisesouter cylinder103 havingfirst end104aand second end104b(not shown), as well asfirst opening105aandsecond opening105b.First and second openings105 are preferably disposed near the center ofcylinder103 and approximately 180° apart. Anchor102 further comprises first rod or paddle106aand second rod or paddle106b,both of which are disposed withinouter cylinder103 and coupled to the first and second ends ofcylinder103 bypins107, which pass through pivot holes108. In this manner, first and second paddles106 are able to rotate about pivot holes108: Paddles106 may be formed, for example, from stainless steel or a polymer, and are separated from one another by gap G. As with the previous anchor assemblies, the precise shape, size and materials of the anchors, as well assuture39, may vary as required for specific applications.
• Suture39 illustratively passes fromdistal anchor62 throughfirst opening105aof proximal anchor102, aroundsecond paddle106b,aroundfirst paddle106a,betweenpaddles106aand106b,and out throughsecond opening105b.The placement of pivot holes108 ensures that application of force F₁, as described hereinabove, causes paddles106 to rotate apart from one another and expand gap G, thereby enabling unidirectional adjustment. Likewise, application of previously discussed force F₂causes paddles106 to rotate together, thereby closing gap G and pinchingsuture39 between the paddles in a friction lock. An increase in the magnitude of force F₂serves to rotate paddles106 together more tightly, thereby increasing the magnitude of the friction lock acting uponsuture39 between the paddles. In this manner, unidirectional adjustment is achieved.
• Referring now toFIG. 13, an alternative unidirectionally adjustable anchor assembly comprising spring material is described.Anchor assembly110 comprisesdistal anchor62 andproximal anchor112. Unidirectionally adjustableproximal anchor112 comprisesouter cylinder113 havingfirst end114aand second end114b(not shown), as well asfirst opening115aandsecond opening115b.First and second openings115 are preferably disposed near the center ofcylinder113 and approximately 180° apart.Anchor112 further comprisesfirst rod116aandsecond rod116bthat are separated by gap G, as well asspring material118, all of which are disposed withinouter cylinder113.Spring material118 abuts rods116, which preferably are substantially the same length ascylinder113, and may either move freely withincylinder113 or may be coupled to the ends (not shown) ofcylinder113.Spring material118 may also move freely withincylinder113 or may be coupled to the cylinder, and compriseslumen119 having a diameter that is preferably equal to or less than the diameter ofsuture39.Spring material118 may comprise, for example, a compressible biocompatible foam, which acts as a compression spring.
• Suture39 passes fromdistal anchor62 toproximal anchor112 throughfirst opening115aofcylinder113, between rods116, throughlumen119 ofspring material118, and out throughsecond opening115b.Lumen119 snugly contacts suture39 such that application of force F₁causes friction between the suture and the spring material to compress the spring material against the wall of cylinder114, thereby reducing a stress applied to rods116 byspring material118 and increasing gap G such that unidirectional adjustment of length L ofsuture39 disposed betweendistal anchor62 and proximal anchor102 may proceed. Application of force F₂stretchesspring material118 against rods116, thereby increasing the stress applied to the rods by the spring material and closing gap G such thatsuture39 is friction locked between rods116.
• With reference toFIG. 14, alternative unidirectionally adjustable anchor assemblies comprising one-way valves are described. InFIG. 14A,anchor assembly120 comprisesdistal anchor62 and proximal anchor122. Unidirectionally adjustable proximal anchor122 comprisesouter cylinder124 having first and second ends125aand125b,as well asfirst opening126aandsecond opening126b.First and second openings126 are preferably disposed near the center ofcylinder124 and approximately 180° apart. Anchor122 further comprises firstinclined plane128aand secondinclined plane128b,which are forced into apposition bycompression springs129aand129b,thereby forming one-way valve V at the junction of the two inclined planes. Inclined planes128 and springs129 are disposed withinouter cylinder124; springs129 abut ends125 ofcylinder124, as well as the ends of the inclined planes.Suture39′ comprises a plurality of knots or beads B adapted to actuate one-way valve V.
• Suture39′ passes fromdistal anchor62 to proximal anchor122 throughfirst opening126aofcylinder124, between inclined planes128, through one-way valve V, and out throughsecond opening126b.Application of force F₁to suture39′ causes a bead B to contact inclined planes128 and gradually coax them apart by compressing springs129, thereby opening valve V and allowing the bead to pass through the valve. Once the bead has passed through valve V, springs129 force inclined planes128 back into apposition, thereby closing the valve. Continued application of force F₁allows multiple beads to pass through the valve, which facilitates unidirectional adjustment of suture length L disposed betweendistal anchor62 and proximal anchor122. Application of force F₂causes a bead B ofsuture39′ to impinge upon the proximal sides of inclined planes128. However, force transferred to the planes by the bead is perpendicular to the direction required to compress springs129 and urge planes128 apart. As such, the bead B impinging upon the proximal sides of planes128 is not able to open one-way valve V and pass back through the valve in a distal direction, thereby ensuring only unidirectional adjustment, i.e. shortening, of the length L of suture disposed between the proximal and distal anchors.
• InFIG. 14B, an alternative unidirectionally adjustable anchor having a one-way valve is described.Anchor assembly130 comprisesdistal anchor62 andproximal anchor132. Unidirectionally adjustableproximal anchor132 compriseslumen134 having cantileveredinclined plane136 disposed therein, which forms one-way valve V. ‘Zip-tie’fastener138, having a plurality ofinclined planes139, connectsproximal anchor132 anddistal anchor62. The plurality ofinclined planes139 are disposed about 180° out of phase withinclined plane136 ofanchor132.
• Fastener138 passes fromdistal anchor62 toproximal anchor132, throughlumen134 and pastinclined plane136.Inclined planes139 offastener138 mesh withinclined plane136 and bend orcantilever plane136, such thatplanes139 offastener138 may proximally pass one-way valve V when force F₁is applied to the fastener, thereby enabling unidirectional adjustment of length L offastener138 disposed between the proximal and distal anchors. Conversely, when force F₂is applied to the fastener, the proximal side ofinclined plane136 ofanchor132 abuts the distal side of an inclined plane1390 offastener138, and the fastener cannot be drawn distally throughproximal anchor132, nor can the length L of fastener disposed between the anchors be increased significantly.
• Referring now toFIG. 15, alternative3 unidirectionally adjustable anchor assemblies comprising a slipknot are described. InFIG. 15A,anchor assembly140 comprisesdistal anchor142 andproximal anchor144. Through-holes143aand143bextend throughdistal anchor142, while through-holes145aand145bextend through proximal anchor145. Preferably, through-holes143 and145 are located near the center ofanchors142 and144, respectively.
• The distal end ofsuture39 passes through through-hole145aofproximal anchor144 todistal anchor142, where it passes through through-hole143aand back through through-hole143b.It then extends fromdistal anchor142 back toproximal anchor144, where it passes through through-hole145bof the proximal anchor. The distal end ofsuture39 is tied off at unidirectional slipknot S, which is located proximal ofanchor144.FIG. 15B provides a detail view illustrating formation of slipknot S.
• As will be apparent to those of skill in the art, application of force F₁causessuture39 to slide through through-holes143 and145, and decrease the length L ofsuture39 disposed betweenanchors142 and144.Suture39 may readily pass through slipknot S in a proximal direction, thereby facilitating unidirectional adjustment of length L. However, application of force F₂tightens slipknot S and prohibits passage ofsuture39 through the slipknot in a distal direction, thereby precluding an increase in length L.
• FIG. 15C illustrates an alternative embodiment ofanchor assembly140 wherein the slipknot is disposed within the proximal anchor.Anchor assembly140′ comprisesdistal anchor142 andproximal anchor144′.Proximal anchor144′ comprises hollow cylinder ortube146 havingdistal openings147aand147b,andproximal opening148.
• The distal end ofsuture39 passes throughproximal opening148 into the interior oftube146. It then passes throughdistal opening147aofproximal anchor144′ todistal anchor142, where it passes through through-hole143aand back through through-hole143b.Next,suture39 extends fromdistal anchor142 back toproximal anchor144′, where it passes throughdistal opening147binto the interior oftube146 of the proximal anchor. The distal end ofsuture39 is tied off at unidirectional slipknot S, which is disposed withintube146 ofanchor144′.Anchor assembly140′ may be unidirectionally adjusted in a manner similar to that described hereinabove with respect toanchor assembly140 ofFIG. 15A.
• FIGS. 7-15 have illustrated anchor assemblies comprising various mechanisms for achieving unidirectional adjustment of the distance between the proximal and distal anchors. These mechanisms have been provided solely for the sake of illustration and should in no way be construed as limiting. Additional mechanisms for achieving unidirectional adjustment will be apparent to those of skill in the art in view of this disclosure and are included in the present invention. Furthermore, a majority of the anchor assemblies ofFIGS. 7-15 have been described with the distal anchor being fixed relative to the suture, and the proximal anchor being adjustable. However, it should be understood that the distal anchor may alternatively be adjustable and the proximal anchor may be fixed, and/or both anchors may be unidirectionally adjustable, as withanchor assembly140 ofFIG. 15.
• With reference now toFIG. 16, a bi-directionally adjustable anchor assembly comprising a locking mechanism is described.Anchor assembly150 comprisesdistal anchor62 andproximal anchor152. As seen inFIG. 16A, bi-directionally adjustableproximal anchor152 comprisesouter cylinder153 havingfirst end154aandsecond end154b,as well asfirst opening155aandsecond opening155b.First and second openings155 are preferably disposed near the center ofcylinder153 and approximately 90° apart.Proximal anchor152 further comprisestension spring158 disposed withinouter cylinder153.
• As seen inFIG. 16B,suture39 passes fromdistal anchor62 toproximal anchor152 throughfirst opening155a,aroundspring158, and out throughsecond opening155b.Suture39 moves freely abouttension spring158 in either direction during application of force F₁or force F₂, thereby facilitating bi-directional adjustment of suture length L disposed between the proximal and distal anchors. However, as seen inFIG. 16C, simultaneous application of forces F₁and F₂with sufficient magnitude causessuture39 to force threads T ofspring158 apart, such thatsuture39 is trapped between threads T and locked in position, thereby precluding further adjustment of suture length L.
• The magnitude of forces required to actuate the locking mechanism ofproximal anchor152 and locksuture39 within threads T ofspring158 may be specified/altered in a variety of ways. For example, the angular spacing of openings155 aboutouter cylinder153 may be altered, the spring constant ofspring158 may be specified, and/orspring158 orsuture39 may comprise a lubricious coating. Additional techniques will be apparent to those of skill in the art. It is expected that simultaneous application of forces F₁and F₂will be encountered whenanchor assembly150 has been deployed across a tissue fold and suture length L has been adjusted such that the tissue fold is compressed. A medical practitioner would then apply force F₁while the compressed tissue fold would apply force F₂.
• Although the anchor assemblies ofFIGS. 10-16 have illustratively been described without knots or loops of suture or fastener disposed proximal of the proximal anchor (as seen, for example, withknot69 onsuture39 ofanchor assembly60 inFIGS. 7 and 8) it should be understood that such loops or knots optionally may be provided in order to facilitate deployment and/or adjustment of the anchor assemblies. Additionally, the previously described anchor assemblies illustratively comprise distal rod- or T-type anchors. However, it should be understood that distal T-anchors have only been provided for the sake of illustration. The distal anchors (as well as the proximal anchors) may comprise any of a variety of anchors, per se known, including, for example, surgical or endoluminal clips, clips for securing tissue and suture knots or knot replacements. Exemplary anchors are described in co-pending U.S. patent application Ser. No. 10/612,170, filed Jul. 1, 2003, which is incorporated herein by reference in its entirety. Furthermore, anchor assemblies may comprise multiple components that are not initially coupled to one another; the components may be brought together and/or coupled within a patient at a treatment site. Additional anchors are described hereinbelow with respect toFIG. 17.
• Referring toFIG. 17A, articulatinganchor160 includessemi-cylindrical base161,rod162 andsuture39.Rod162 rotates about pivot point163 (as indicated by arrow164) between an expanded position (shown inFIG. 7A) and a reduced profile position, whereinrod162 pivots within thesemi-cylindrical base161. Articulatinganchor160 may be delivered through a tissue fold using, for example,needle34 described hereinabove with respect toFIG. 3E. Preferably, articulatinganchor160 is biased in the expanded position so that it automatically expands once it is ejected from the needle.
• With respect toFIGS. 17B and 17C the anchors of the present invention also may comprise one or more oblong bodies connected by at least one suture. InFIG. 17B,anchor165 compriseselliptical ring166 havingsutures39 attached at substantially opposite sides of the ring. InFIG. 17C,anchor168 comprisesangle bracket169 having a pair of through-holes170 forsuture39. InFIG. 17D,anchor171 comprisesoblong bead172 having a pair of through-holes173 forsuture39. All threeanchors165,168 and171 (as well as the T-anchors described previously) have a first dimension (e.g., width) that is substantially larger than a second dimension (e.g., height). This dimensional difference necessitates that anchors165,168 and171 be inserted within a needle (e.g.,needle34 ofFIG. 3E) in a particular orientation. Once the anchor is ejected through a tissue wall, tension onsuture39 forces the anchor to rotate so that it cannot be pulled back through the tissue wall. As will be understood by those of skill in the art, numerous other anchors may be employed without departing from the scope of the present invention.
• Referring now toFIG. 18A, an alternative embodiment of apparatus for forming a tissue fold, constructed in accordance with the principles of the present invention, is described.Apparatus175 comprisestreadmill assembly176 disposed atdistal tip174 offlexible tube177.Flexible tube177 is configured to be inserted through a patient's mouth, esophagus and into the stomach.Treadmill assembly176 comprisesconveyor180 that circles around a pair ofhubs181aand181b.Hubs181aand181brotate aboutaxles182aand182b,respectively, and are interconnected bybracket183. A plurality of barbs orneedles185 is disposed at substantially regular intervals around the circumference ofconveyor180.
• Flexible tube177 preferably includes a plurality of through-wall slots186 to enhance flexibility of the tube, yet maintain torqueability. Preferably,flexible tube177 is made from stainless steel with an etched or laser-cut slot pattern. Preferably, the slot pattern is a sinusoidal repeating pattern of slots perpendicular to the longitudinal axis of the tube. Additional and/or alternative patterns will be apparent to those of skill in the art.
• Referring toFIGS. 18 and 19, transmission of motive force totreadmill assembly176 is described. In particular, driveshaft202 disposed withinflexible tube177 is coupled to a manual knob or motor located at the proximal end of the catheter. The distal tip ofdrive shaft202 is provided withbeveled gear203 that meshes withbeveled gear204 provided onaxle182b.Accordingly, rotation ofbeveled gear203 is transmitted tobeveled gear204, thereby causingaxle182bto rotate.Axle182bin turn rotateshub181b,actuatingconveyor180. Reversing the rotation ofdrive shaft202 reverses the direction ofconveyor180.
• Referring again toFIGS. 18A-18D, a method of forming a gastrointestinal tissue foldF using apparatus175 is described. InFIG. 18A,flexible tube177 is positioned transesophageally so thattreadmill assembly176 contacts tissue wall W. Preferably, contact should be made at an angle relative to the tissue wall W. For example, an angle of approximately 45 degrees is depicted inFIG. 8A, while many other angles may be used without departing from the scope of the present invention.
• Whentreadmill assembly176 contacts tissue wall W,needle185 engages the tissue at contact point P1 as the needle moves arounddistal hub181a.As depicted inFIG. 18B, as the needle moves away fromdistal hub181a,tissue wall W is pulled towardsproximal end181b,thereby forming a small tissue fold F. As the treadmill assembly continues to turn,subsequent needles185 engage the tissue wall so that it becomes securely engaged totreadmill assembly176 along the length ofconveyor180.
• As depicted inFIG. 18C, once tissue wall W is securely engaged totreadmill assembly176,distal end174 offlexible tube177 may be articulated inbendable section190, thereby movingtreadmill assembly176 away from tissue wall W. The articulation offlexible tube177 may be accomplished using a control wire and actuator disposed at the proximal end of the catheter, as previously described with respect to the embodiment ofFIG. 1. By moving the treadmill assembly away from tissue wall W, additional tissue is pulled proximally and tissue fold F becomes elongated.
• InFIG. 18D, tissue fold F is stretched acrossbendable section190 offlexible tube177 to create contact point P2. This permits a sharpened needle or obturator to be extended through one ofslots186 ofbendable section190 and across all four layers of the tissue wall W. Advantageously, stretching of tissue fold F acrossbendable section190 permits an anchor to be ejected through both the muscularis and serosa layers, thus providing a durable foundation for gastrointestinal tissue approximation. For example,needle192 may be extended throughslot186 inbendable section190, and through the base of tissue fold F, and an anchor assembly (such as described with respect to any ofFIGS. 4-17) may be ejected fromneedle192 to secure the fold. Alternatively, an obturator (such as described with respect toFIGS. 5A and 5B) may be used to pierce the tissue fold at contact point P2 and deliver the anchor assembly.Treadmill assembly176 may be disengaged from tissue wall W by reversing the rotation ofproximal hub181b.
• Referring now toFIG. 20A, a further alternative embodiment of apparatus for forming a tissue fold in accordance with the principles of the present invention is described.Apparatus200 comprisestissue grabbing assembly18′ coupled to the distal end of aflexible tube177′, such as described with respect to the embodiment ofFIG. 18.Flexible tube177′ preferably includes a plurality of through-wall slots186′ to enhance flexibility of the tube, yet maintain torqueability. In addition,flexible tube177′ may be made from stainless steel with an etched or laser-cut slot pattern, such as a sinusoidal repeating pattern of slots perpendicular to the longitudinal axis of the tube. Alternative flexible patterns will be apparent.
• Tissue grabbing assembly18′ is similar to that described with respect to the embodiment ofFIG. 1, and comprises a pair ofjaws28a′,28b′ arranged to rotate aboutpivot point29′ between an open configuration and a closed configuration. Each ofjaws28a′,28b′ preferably includes sharpenedteeth33′ disposed near its distal end to facilitate grasping tissue wall W.
• With respect toFIG. 20A,tissue grabbing assembly18′ is positioned transesophageally adjacent to tissue wall W andjaws28a′,28b′ are moved to the open position.Tissue grabbing assembly18′ then is moved into contact with tissue wall W. As depicted inFIG. 20B,tissue grabbing assembly18′ is used to grab the tissue wall at a first contact point P1. After capturing a portion of tissue wall W withinjaws28a′,28b′,flexible tube177′ is urged proximally to stretch tissue wall W and create tissue fold F.
• Referring toFIG. 20C, once tissue fold F is formed, the distal end offlexible tube177′ is articulated aboutbendable section190′ to movetissue grabbing assembly18′ away from tissue wall W. Articulation offlexible tube177′ may be controlled using an actuator disposed at the proximal end of the catheter, thus causing tissue fold F to become elongated.
• InFIG. 20D, tissue fold F is shown stretched acrossbendable section190′ so that a sharpened needle or obturator may be extended from one ofslots186′ inbendable section190′ and across all four layers of the tissuewall W. Needle192′ then may be extended fromslot186′ inbendable section190′ through contact point P2 and tissue fold F. An anchor assembly (e.g., as described with respect to any ofFIGS. 4-17) then may be ejected fromneedle192′ to secure the fold. Alternatively, an obturator (e.g., as described with respect toFIGS. 5A and 5B) may be used to pierce the tissue fold at contact point P2 and deliver the anchor assembly.
• With reference now toFIG. 21, an anchor delivery system adapted for use with the adjustable anchor assemblies ofFIGS. 7-17 is described. InFIG. 21, the anchor delivery system is illustratively shown in use withanchor assembly60 ofFIG. 7, but this should in no way be construed as limiting. Also, the delivery system ofFIG. 21 may be used in conjunction with apparatus for forming a tissue fold, such asapparatus10,175 and200 described previously, or alternative apparatus described hereinafter, in order to anchor the tissue fold. Alternatively, the delivery system may be used for any other application, or in conjunction with any other apparatus, requiring delivery of an anchor assembly.
• InFIG. 21A, a distal region ofanchor delivery system250 is disposed adjacent tissue fold F in tissue wall W.Anchor delivery system250 comprisesflexible delivery tube252 havinglumen253.Flexible delivery tube252 may be configured for insertion through a patient's mouth and esophagus into a gastrointestinal lumen, such as the stomach.Lumen253 ofdelivery tube252 preferably has a diameter of less than about 5 mm, and even more preferably has a diameter of about 2-3 mm.Flexible delivery tube252 preferably includes a plurality of through-wall slots254 to enhance flexibility of the tube, yet maintain torqueability.Slots254 may formbendable section255. Preferably,flexible delivery tube252 is made from stainless steel with an etched or laser-cut slot pattern. The slot pattern is preferably a sinusoidal repeating pattern of slots perpendicular to the longitudinal axis of the tube. Additional and/or alternative patterns will be apparent.
• Anchor delivery system250 further comprisesdelivery needle260.Needle260 preferably has a length of less than 2 cm, and even more preferably has a length of about 1.5 cm.Needle260 preferably comprises sharpeneddistal tip262,lumen264,slot266 extending proximally fromdistal tip262, andproximal eyelet268.
• Lumen264 ofneedle260 is dimensioned such that a distal anchor may be disposed therein. As discussed previously,anchor delivery system250 is illustratively described in conjunction withanchor assembly60 ofFIG. 7. InFIG. 21A,distal anchor62 is disposed withinlumen264 ofneedle260.Suture39 passes throughslot266 of the needle as the suture extends fromdistal anchor62 toproximal anchor64.Needle260 preferably is disposed withinlumen253 offlexible delivery tube252 distal ofbendable section255, whileproximal anchor64 preferably is disposed withindelivery tube252 proximal ofbendable section255.
• In this arrangement,distal anchor62 may be deployed throughneedle260 while the bendable section is actuated or bent, e.g., whenanchor delivery system250 is used in conjunction with previously described plication apparatus.Proximal anchor64 subsequently may be advanced throughbendable section255 after the bendable section has once again been straightened. The distance, or length, ofsuture39 extending betweendistal anchor62, which is disposed distal of the bendable section, andproximal anchor64, which is disposed proximal of the bendable section, is preferably greater than or equal to about 2 cm, and is even more preferably greater than or equal to about 4 cm.
• Needle260 is proximally coupled toneedle pushrod270, which facilitates translation of the needle beyond a distal end offlexible delivery tube252.Needle pushrod270 extends to a control actuator disposed at a proximal end of anchor delivery system250 (not shown).Pushrod270 optionally may be spring-loaded (not shown), for example, to facilitate puncture of tissue wall W and passage ofneedle260 through tissue fold F.
• Anchor delivery system250 further comprisesanchor pushrod280, which is removably disposed througheyelet268 ofneedle260, and is configured to ejectdistal anchor62 fromlumen264 ofneedle260. As withneedle pushrod270,anchor pushrod280 extends to a control actuator disposed at a proximal end of anchor delivery system250 (not shown). Theactuators controlling pushrods270 and280 are preferably at least partially coupled so that relative motion between the two pushrods can be limited and/or eliminated, as needed.Pushrod280 passes through the proximal loop of suture formed byknot69 onsuture39, such that the suture loop is threaded betweenneedle pushrod270 andanchor pushrod280. This facilitates unidirectional adjustment of the length of suture disposed betweendistal anchor62 andproximal anchor64, as described hereinbelow.
• InFIG. 21B,pushrods270 and280 are simultaneously distally advanced with sufficient force, e.g., via spring-loading, such that sharpeneddistal tip262 ofneedle260 pierces tissue wall W and is advanced across foldF. Bendable section255 offlexible delivery tube252 optionally may be bent during advancement of the needle, as described previously with respect to the plication apparatus (seeFIG. 3E).Anchor pushrod280 is then advanced distally with respect toneedle pushrod270 andneedle260, such that it abutsdistal anchor62 and ejects the anchor fromlumen264 ofneedle260 on the distal side of tissue fold F, as seen inFIG. 21C.Suture39 likewise is ejected fromslot266 and disposed across fold F.
• During delivery, the longitudinal axis ofdistal anchor62 is substantially parallel to the longitudinal axis ofneedle260. However, onceanchor62 has been ejected fromneedle260, suture tension induces the anchor to rotate approximately 90° about its longitudinal axis, so that its longitudinal axis is substantially perpendicular to the longitudinal axis ofneedle260. This rotation ofdistal anchor62 prevents it from being pulled back through tissue wall W. One or both ends ofanchor62 may be flared outward (not shown) to facilitate such rotation upon contact with the tissue wall.
• InFIG. 21D,anchor pushrod280 is retracted proximally withinlumen264 ofneedle260, the needle is retracted within flexiblydelivery tube252 viapushrod270, and thendelivery system250 is retracted proximally across tissue foldF. Distal anchor62 is disposed on the distal side of the tissue fold,suture39 extends through the fold, andproximal anchor64 is disposed on the proximal side of the fold withindelivery tube252. Ifbendable section255 were flexed during deployment of distal anchor62 (seeFIG. 3E), it is straightened to facilitate delivery of the proximal anchor.
• Delivery tube252 is then retracted proximally with respect topushrods270 and280, causingneedle260 to exitlumen253 of the delivery tube on the proximal side of tissue fold F, thereby providing space forproximal anchor64 to exit the lumen. Next,delivery tube252 or thefull delivery system250 is retracted, such thatproximal anchor64 is ejected fromdelivery tube lumen253, as seen inFIG. 21E.Delivery tube252 is then re-advanced and/orpushrods270 and280 are simultaneously retracted, such thatneedle260 is repositioned withinlumen253 of the delivery tube.
• Flexible delivery tube252 is advanced with respect toneedle260, such that it pushesproximal anchor64 distally. The proximal suture loop formed byknot69 onsuture39 catches against the proximal end ofneedle260 andanchor pushrod280, which pullsdistal anchor62 taut against tissue fold F, as seen inFIG. 21F. Continued advancement ofdelivery tube252 unidirectionally adjusts, i.e. shortens, length L ofsuture39 disposed betweendistal anchor62 andproximal anchor64, while forcingproximal anchor64 against the tissue fold and firmly anchoring the fold between the proximal and distal anchors.
• Once length L has been adjusted such thatanchor assembly60 firmly anchors tissue fold F in position,anchor pushrod280 may be retracted proximally with respect toneedle pushrod270 andneedle260, such that the distal end ofanchor pushrod280 is proximally retracted througheyelet268 and out ofneedle260. As seen inFIG. 21G, the suture loop formed byknot69 onsuture39 slips off the distal end ofanchor pushrod280, removinganchor assembly60 fromanchor delivery system250.Anchor delivery system250 may then be removed from the patient. Alternatively,needle260,needle pushrod270 andanchor pushrod280 may be proximally retracted and removed fromlumen253 ofanchor delivery tube252. Anadditional anchor assembly60 may then be reloaded withinneedle260 anddelivery tube252 from a proximal end of the delivery tube, while a distal end of the delivery tube remains within the patient. The additional anchor assembly may, for example, be placed across an additional tissue fold.
• Delivery system250 optionally may comprise cutting apparatus (not shown) for removing the portion of suture extending proximally ofproximal anchor64 post-adjustment. Alternatively, secondary apparatus may be provided to remove such proximal length of suture. As yet another alternative, the unneeded length of suture may be left within the patient post-procedure.
• In order to decrease the number of steps required to deliver and adjustanchor assembly60, oncedistal anchor62 has been deployed, as inFIG. 21C, the entireanchor delivery system250 may be retracted proximally, such thatneedle260 is retracted across tissue fold F while still disposed outside ofdelivery tube lumen253. This is in contrast to the method described with respect toFIG. 21D, wherein the needle is disposed within the delivery tube prior to retraction across the tissue fold. Continued proximal retraction ofanchor delivery system250 ordelivery tube252 deploysproximal anchor64 fromdelivery tube lumen253.Anchor assembly60 then may be unidirectionally adjusted, as described previously.
• Anchor delivery system250 advantageously provides a medical practitioner with significant control during all steps of anchor assembly deployment. Such control affords the medical practitioner ample opportunity to abort deployment of the anchor assembly. Upon passage ofneedle260 across tissue fold F, as seen inFIG. 21B, the medical practitioner may decide to retract the needle across the fold and not launch the distal anchor. Alternatively, after deployment of thedistal anchor62, as seen inFIG. 21D, the medical practitioner may decide not to deploy the proximal anchor and may sever the suture connecting the proximal and distal anchors. The distal anchor then would simply pass harmlessly through the patient's digestive system. As yet another example, the medical practitioner may decide not to cinch the proximal and distal anchors post-deployment, thereby leaving the anchors in place without securing tissue fold F. Furtherstill, the medical practitioner may reverse cinching or cut the anchor assembly post-deployment, thereby reversing tissue fold formation.
• As will be apparent to those of skill in the art, whenanchor delivery system250 is used in conjunction with previously describedapparatus10,175 or200, to place an anchor assembly across fold F formed by said apparatus,flexible delivery tube252 may either comprise or be advanced throughflexible tube14,177 or177′, ofapparatus10,175 or200, respectively. Likewise,needle260 may compriseneedle34,92 or92′, ofapparatus10,175 or200, respectively.Needle260 alternatively may compriseobturator50 ofFIG. 5. As will be apparent, components ofanchor delivery system250 may also comprise or be advanced through comparable components of alternative tissue folding apparatus described hereinafter.
• Referring now toFIG. 22, an alternative anchor delivery system is described. As withanchor delivery system250 ofFIG. 21,anchor delivery system300 ofFIG. 22 is adapted for use with the adjustable anchor assemblies ofFIGS. 7-17. InFIG. 22, theanchor delivery system300 is illustratively shown in use withanchor assembly60 ofFIG. 7, but this should in no way be construed as limiting. Also,delivery system300 may be used in conjunction with apparatus for forming a tissue fold, such asapparatus10,175 and200 described previously, or alternative apparatus described hereinafter, in order to anchor the tissue fold. Alternatively, the delivery system may be used for any other application, or in conjunction with any other apparatus, requiring delivery of an anchor assembly.
• FIG. 22A illustrates a distal region ofanchor delivery system300.System300 comprisesflexible delivery tube302 havinglumen303.Flexible delivery tube302 may be configured for insertion through a patient's mouth and esophagus into a gastrointestinal lumen, such as the stomach.Flexible delivery tube302 preferably includes a plurality of through-wall slots304 to enhance flexibility of the tube, yet maintain torqueability.Slots304 may formbendable section305. Preferably,flexible delivery tube302 is made from stainless steel with an etched or laser-cut slot pattern. The slot pattern is preferably a sinusoidal repeating pattern of slots perpendicular to the longitudinal axis of the tube. Additional/alternative patterns will be apparent to those of skill in the art.
• Flexible delivery tube302 further comprisesend region306, which is coupled to anchortube307 having lumen or bore308. As best seen inFIG. 22B,lumen308 ofanchor tube307 communicates withlumen303 ofdelivery tube302 via through-slot309.Proximal anchor64 is disposed withinanchor tube307, whiledistal anchor62 is disposed withinneedle260′, which sits withindelivery tube302.
• Suture39 passes out ofneedle260′ fromdistal anchor62 throughslot266′. It then crosses fromflexible delivery tube302 to anchortube307 via through-slot309. After passing throughproximal anchor64,suture39 is passed back todelivery tube302 via the through-slot, and is threaded aroundanchor pushrod280′, such that the loop of suture formed byknot69 onsuture39 is disposed betweenpushrod280′.
• Needle260′,needle pushrod270′ andanchor needle pushrod270′ andanchor pushrod280′ arepushrods270 and hereinabove with substantially the same asneedle260 and280, respectively, which are described respect to anchordelivery system250 ofFIG. 21. Furthermore,anchor assembly60 may be delivered from and adjusted byanchor delivery system300 in a manner similar to that described hereinabove with respect tosystem250.
• InFIG. 22A,anchor tube307 ofanchor delivery system300 is illustratively shown as a relatively short tube having lumen or bore308 adapted for disposal ofproximal anchor64 therein. However, it should be understood thatanchor tube307,lumen308 and/or through-slot309 alternatively may extend all or part of the way to a proximal end offlexible delivery tube302 ofdelivery system300. Advantageously, such an arrangement facilitates loading ofanchor assembly60 from a proximal end of the anchor delivery system, e.g., for reloading ofanchor delivery system300 while a distal region of the system is disposed within a patient. Such an arrangement also may simplify manufacturing of the system.
• Anchor delivery system300 illustratively has been described with asingle anchor assembly60 disposed therein. However, it should be understood that a plurality of anchor assemblies may be loaded withindelivery system300, thereby facilitating delivery of multiple anchor assemblies across different points of a tissue fold, across different (e.g., adjacent) tissue folds, or across other tissue structures. The plurality ofdistal anchors62 preferably are loaded withinneedle262′ offlexible delivery tube302, while the plurality ofproximal anchors64 preferably are loaded withinlumen308 ofanchor tube307.
• An advantage ofanchor delivery system300, as compared tosystem250 ofFIG. 21, is that both the proximal and distal anchors are located distal of the bendable section of the delivery tube during delivery. This reduces an initial length of suture that must be disposed between the anchors, thereby reducing a length of unneeded suture extending proximally of the proximal anchor post-delivery and adjustment. It also simplifies delivery by allowing both the proximal and distal anchors to be delivered while the bendable section of the delivery tube is bent. Additionally, placement of the proximal anchor in a separate anchor tube eliminates a need to eject the needle from the flexible delivery tube on the proximal side of a tissue fold in order to deploy the proximal anchor, thereby reducing a risk of accidental tissue puncture with the needle.
• With reference toFIG. 23, another alternative anchor delivery system is described. As withanchor delivery systems250 and300 ofFIGS. 21 and 22, respectively,anchor delivery system400 ofFIG. 23 is adapted for use with the adjustable anchor assemblies ofFIGS. 7-17.Anchor delivery system400 is illustratively shown in use withanchor assembly60 ofFIG. 7, but this should in no way be construed as limiting. Also,delivery system400 may be used in conjunction with apparatus for forming a tissue fold, such asapparatus10,175 and200 described previously, or alternative apparatus described hereinafter, in order to anchor the tissue fold. Alternatively,delivery system400 may be used for any other application, or in conjunction with any other apparatus, requiring delivery of an anchor assembly.
• FIG. 23 illustrates a distal region ofanchor delivery system400.System400 comprisesflexible delivery tube402 havinglumen403.Flexible delivery tube402 may be configured for insertion through a patient's mouth and esophagus into a gastrointestinal lumen, such as the stomach.Flexible delivery tube402 preferably includes a plurality of through-wall slots to enhance flexibility of the tube, yet maintain torqueability. The slots may formbendable section405.
• Anchor delivery system400 further comprisesdelivery needle260″, which is disposed withinlumen403 offlexible delivery tube402 distal ofbendable section405 during delivery. As discussed previously,anchor delivery system400 is illustratively described in conjunction withanchor assembly60 ofFIG. 7.Needle260″ preferably has a length sufficient for bothdistal anchor62 andproximal anchor64 ofanchor assembly60 to be disposed therein; for example,needle260″ preferably has a length of less than about 5 cm, and even more preferably has a length of about 3 cm. Except for an increase in length,needle260″ is substantially the same asneedle260 ofFIG. 21.
• InFIG. 23, bothdistal anchor62 andproximal anchor64 are disposed withinlumen264″ ofneedle260″.Suture39 passes through and back throughslot266″ of the needle as the suture extends fromdistal anchor62 toproximal anchor64. Alternatively the length of suture between the proximal and distal anchors may be disposed within the needle during delivery. Advantageously, both the proximal and distal anchors ofanchor assembly60 may be deployed throughneedle260″ whilebendable section405 is actuated or bent, e.g., whileanchor delivery system400 is used in conjunction with previously described plication apparatus.
• Needle260″ is proximally coupled toflexible needle pushtube420, which facilitates translation of the needle beyond a distal end offlexible delivery tube402. As will be apparent to those of skill in the art,needle260″ and needle pushtube420 optionally may be manufactured as a single piece.Needle pushtube420 compriseslumen422, as well asskive424 that communicates withlumen422.Needle pushtube420 extends to a control actuator (not shown), which may be spring-loaded, disposed at a proximal end ofanchor delivery system400.
• Anchor pushrod280″, which is substantially the same asanchor pushrod280 described previously, is removably disposed withinlumen422 ofneedle pushtube420 distal ofskive424. As withpushtube420,anchor pushrod280″ extends to a control actuator (not shown) disposed at a proximal end of the anchor delivery system.Suture39 proximally extends fromproximal anchor64 throughslot266″ ofneedle260″, throughskive424 and withinlumen422 ofneedle pushtube420, aroundanchor pushrod280″ and out throughskive424 toknot69. The proximal loop of suture formed byknot69 is trapped aroundpushrod280″ and withinlumen422 of the needle pushtube, thereby facilitating unidirectional adjustment of the length of suture disposed betweendistal anchor62 andproximal anchor64. As an alternative to the proximal loop of suture,knot69 may be formed on the proximal end ofsuture39, such that the knot is trapped between anchor pushtube280″ and needle pushrod420 (see knot K ofFIG. 24).
• Anchor assembly60 may be delivered, deployed and adjusted byanchor delivery system400 in a manner similar to that described hereinabove with respect tosystem250 ofFIG. 21, with a few alterations. Specifically, during deployment ofdistal anchor62,anchor pushrod280″ is advanced againstproximal anchor64, which in turn advances in-linedistal anchor62. The pushrod is advanced a sufficient distance with respect toneedle260″ to eject the distal anchor fromneedle lumen264″, but not so far as to also prematurely ejectproximal anchor64. Motion limitation apparatus may be provided to ensure that the distal anchor is not prematurely ejected. Exemplary motion limitation apparatus is described hereinbelow with respect toFIG. 24; additional apparatus, per se known, will be apparent.
• In order to ejectproximal anchor64 fromlumen264″ ofneedle260″, either the needle is retracted until length L ofsuture39 disposed between the proximal and distal anchors is pulled taut and pulls the proximal anchor out of the needle lumen, oranchor pushrod280″ is advanced a sufficient distance within the lumen ofneedle260″ to eject the proximal anchor from the lumen (or a combination thereof). Additionally, in order to releaseanchor assembly60 fromanchor delivery system400 post-delivery and adjustment,anchor pushrod280″ is retracted proximal ofskive424 such that the loop ofsuture39 formed byknot69 is no longer trapped withinlumen422 ofneedle pushrod420. Upon deployment ofanchor assembly60,delivery system400 may be removed from the patient. Alternatively,needle260″ andneedle pushrod420, as well asanchor pushrod280″, may be removed from the patient, reloaded with a new anchor assembly, and re-advanced throughflexible delivery tube402 for deployment of additional anchors without necessitating removal ofdelivery tube402 from the patient.
• A significant advantage ofanchor delivery system400, as compared tosystem250 ofFIG. 21, is that both the proximal and distal anchors are disposed distal ofbendable section405 offlexible delivery tube402. A significant advantage ofanchor delivery system400, as compared tosystem300 ofFIG. 22, is that both the proximal and distal anchors are disposed withinneedle260″, thereby eliminating a need for an anchor tube and reducing a profile of the system.
• Referring now toFIG. 24, an alternative embodiment ofanchor delivery system400 is described comprising motion limitation apparatus.Anchor delivery system400′ is substantially the same assystem400, except that needle pushtube420′ comprises two skives:motion limitation skive430 andunidirectional adjustment skive432, both of which communicate withlumen422′ of the needle pushrod.Suture39 proximally extends fromproximal anchor64, throughmotion limitation skive430 and withinlumen422′ betweenanchor pushrod280″ and needle pushtube420′.Suture39 exits skive430 and is tied off at motion limitation knot K, which is trapped atskive430 byanchor pushrod280″.Suture39 then continues proximally tounidirectional adjustment skive432 and the proximal loop of suture formed byknot69, which is trapped atskive432 aroundpushrod280″.
• A length of suture extending betweenproximal anchor64 and knot K is specified such thatdistal anchor62 may exit lumen264″ ofneedle260″, butproximal anchor64 cannot exit while knot K is trapped atskive430 byanchor pushrod280″. For example, during delivery ofanchor assembly60 across a tissue fold, advancement ofpushrod280″ advancesproximal anchor64, which in turn advances in-linedistal anchor62 until the distal anchor is ejected fromneedle lumen264″ on the distal side of the tissue fold. Knot K limits adistance anchor pushrod280″ may be advanced and ensures thatproximal anchor64 is not prematurely deployed.
• Onceanchor delivery system400′ is again disposed on the proximal side of the tissue fold,anchor pushrod280″ is retracted proximal ofmotion limitation skive430, thereby allowing knot K to escape fromskive430 and facilitating deployment ofproximal anchor64.Proximal anchor64 may be deployed by either retractingneedle260″ until the length of suture between the two anchors is pulled taut and pulls the proximal anchor out of the needle, or byre-advancing pushrod280″ to push the proximal anchor out of the needle.
• The anchor assembly may then be unidirectionally adjusted via the suture loop trapped at skive232, as described previously. After adjustment has been completed,anchor pushrod280″ is retracted proximal ofunidirectional adjustment skive432, thereby allowing the loop of suture formed byknot69 ofsuture39 to escape fromskive432. As withanchor delivery systems250 and400 described previously, upon deployment of the anchor assembly,system400′ may be removed from the patient, or may be reloaded whileflexible tube402 remains in the patient. A significant advantage ofanchor delivery system400′, as compared tosystem400 ofFIG. 23, is thatmotion limitation skive430 reduces a risk of premature deployment ofproximal anchor64.
• With reference toFIG. 25, yet another alternative anchor delivery system is described.Anchor delivery system500 is adapted to deliver multiple adjustable anchor assemblies without necessitating reloading or removal from a patient.Delivery system500 may be used in conjunction with apparatus for forming a tissue fold or may be used for any other application, or in conjunction with any other apparatus, requiring delivery of an anchor assembly. InFIG. 25,anchor delivery system500 is illustratively loaded withmultiple anchor assemblies60 ofFIG. 7, but this should in no way be construed as limiting.
• FIG. 25 illustrates a distal region ofanchor delivery system500.System500 comprisesflexible delivery tube510,flexible needle tube520,anchor pushrod530 and skiverod540.Delivery tube510, which is substantially the same asdelivery tube402 described previously, compriseslumen511 and optionalbendable section512.Needle tube520 comprisesdelivery needle522,anchor lumen523 and skive bore524.Lumen523 extends throughneedle tube520 from its proximal end toneedle522, andanchor pushrod530, as well asanchor assemblies60, is disposed within the lumen. Bore524 preferably terminates just proximal ofneedle522; skiverod540 is disposed within the bore. For ease of manufacturing, bore524 optionally may be replaced with a lumen (not shown) that extends all the way toneedle522.
• Needle tube520 further comprises two through-slots and two skives: first motion limitation through-slot526a,first unidirectional adjustment skive528a,second motion limitation through-slot526b,and secondunidirectional adjustment skive528b.The skives and through-slots all communicate withskive bore524. Through-slots526 further communicate withanchor lumen523 and provide passageways between the anchor lumen and skive bore524. Skives528 further communicate with the exterior ofneedle tube520 and provide passageways between the exterior and skive bore524.
• As discussed previously,anchor delivery system500 is illustratively shown loaded withanchor assemblies60.First anchor assembly60aandsecond anchor assembly60bare disposed withinanchor lumen523, withassembly60adisposed distal ofassembly60b.Anchor pushrod530 is disposed proximal ofsecond assembly60bwithinlumen523.
• First suture39aoffirst anchor assembly60aproximally extends withinlumen523 from firstdistal anchor62ato and through firstproximal anchor64a.Suture39athen extends fromanchor lumen523 to skivebore524 via first motion limitation through-slot526a.Suture39aloosely encirclesskive rod540 and is tied off to itself at first motion limitation knot K_1A, such that the loop of suture formed by knot K_1A, is trapped aboutskive rod540. A length of suture disposed between firstproximal anchor64aand first motion limitation knot K_1A, is sufficient to allow deployment of firstdistal anchor62afromlumen523 ofneedle tube520, but is not long enough to allow deployment of firstproximal anchor64afrom the lumen. Rather, the length of suture is pulled taut with the loop formed by knot Kam, abutting first through-slot526aand trapped aboutskive rod540. In this manner, the suture loop formed by knot K_1Aprovides motion limitation when disposed aboutskive rod540. Skiverod540 may be translated relative to the suture loop to release the loop from the rod after deployment of firstdistal anchor62a.
• From knot K_1A,first suture39acontinues proximally to first unidirectional adjustment skive528a.Suture39athen once again loosely encirclesskive rod540 and is tied off to itself at first unidirectional adjustment knot K_1B. While disposed aboutskive rod540 atfirst skive528a,the loop of suture formed by knot K_1Bmay be used to unidirectionally adjustfirst anchor assembly60apost-deployment, as described hereinabove. A length of suture disposed between firstproximal anchor64aand first unidirectional adjustment knot K_1Bis sufficient to enable deployment of the anchor fromlumen523 ofanchor tube520.
• Second suture39bofsecond anchor assembly60bcouples seconddistal anchor62band secondproximal anchor64bto second motion limitation through-slot526band secondunidirectional adjustment skive528bin a manner similar to that described with respect tofirst suture39aoffirst anchor assembly60a.The loop of suture formed by second motion limitation knot K_2Aprecludes premature deployment of secondproximal anchor64b,while the loop of suture formed by second unidirectional adjustment knot K_2Benables adjustment of a length of suture disposed between seconddistal anchor62band secondproximal anchor64b.
• Anchor assemblies60aand60bmay be delivered from, and adjusted by,anchor delivery system500 in a manner similar to that described hereinabove with respect tosystem400′ ofFIG. 24, with a few alterations. Specifically, during deployment of firstdistal anchor62a,anchor pushrod530 is advanced against secondproximal anchor64b,which in turn advances in-line seconddistal anchor62band in-line firstproximal anchor64a.The pushrod is advanced a sufficient distance with respect toneedle tube520 to eject firstdistal anchor62afromanchor lumen523.
• Additional advancement ofpushrod530 causes the suture loop formed by first motion limitation knot Ku, to catch against first through-slot526a,thereby ensuring that firstproximal anchor64ais not prematurely ejected fromlumen523. When ready to deploy the first proximal anchor, skiverod540 may be retracted proximal of first motion limitation through-slot526a,thereby freeing the loop of suture formed by knot Ku, from the skive rod. Firstproximal anchor64amay then be deployed by further distal advancement of the anchor pushrod againstsecond anchor assembly60b.The second anchor assembly advances firstproximal anchor64aout ofneedle522.
• First anchor assembly60athen may be unidirectionally adjusted as described hereinabove, usingfirst skive528a,the loop of suture formed by first adjustment knot K_1Banddelivery tube510. Once adjusted,skive rod540 may be further retracted within skive bore524 to a position proximal offirst skive528a,thereby releasingfirst anchor assembly60afromanchor delivery system500.Second anchor assembly60bmay then be deployed and adjusted in a similar manner using second through-slot526b,second skive528band second knots K_2Aand K_2B.
• As will be apparent to those of skill in the art, althoughanchor delivery system500 illustratively has been described in a configuration suited for delivery of only two anchor assemblies, any number of anchor assemblies may be accommodated, for example, by adding additional pairs of motion limitation through-slots and unidirectional adjustment skives toneedle tube520. Additionally, spacers, for example, digestible spacers, wax spacers, polymer spacers, etc., may be provided between anchors and/or between anchor assemblies to reduce a risk of premature deployment of an anchor or assembly. Additional spacing and motion limitation techniques will be apparent.
• Referring now toFIG. 26, an alternative embodiment ofanchor delivery system500 is described. For the purposes of illustration,flexible delivery tube510 has been omitted fromsystem500′ ofFIG.26. However, it should be understood thatanchor delivery system500′ preferably comprisesflexible delivery tube510.
• Anchor delivery system500′ is substantially the same assystem500, except that first and second through-slots526a′ and526b′ do not communicate withskive bore524. Rather, through-slots526′ provide openings betweenanchor lumen523 and the exterior ofneedle tube520. Additionally,needle tube520 further comprises first and second motion limitation skives527aand527b,which constrain the loops of suture formed by first and second motion limitation knots K3j, and K_1A, respectively. It is expected thatanchor delivery system500′ will be easier to manufacture thansystem500. Additionally, enhanced suture management is expected, since a substantial length offirst suture39aandsecond suture39bis disposed outside ofneedle tube520 withinlumen511 of delivery tube510 (seeFIG. 25) during delivery. As withanchor delivery system500,delivery system500′ may be provided with spacers between anchors and/or anchor assemblies to reduce a risk of premature anchor deployment.
• Anchor delivery systems500 and500′ ofFIGS. 25 and 26, respectively, provide for delivery and deployment of multiple adjustable anchor assemblies from a linear stack of anchors disposed within a lumen of the needle tube.FIG. 27 illustrate a first embodiment of an alternative anchor delivery system wherein the multiple anchor assemblies are delivered and deployed from chambers of a radial stack or revolver disposed about the needle tube, without necessitating reloading or removal from the patient. Either the revolver or the needle tube (or both) may be rotated to align the needle tube with successive chambers of the revolver for reloading the needle tube with anchor assemblies from the radial stack.
• InFIG. 27,anchor delivery system600 comprisesflexible delivery tube610,flexible needle tube620,anchor pushrod630 andrevolver640.Flexible delivery tube610 compriseslumen612.Needle tube620 comprisesneedle622,anchor loading slot624,anchor lumen626 and plurality of adjustment skives628.Skives628 are disposed over a longitudinal length ofneedle tube620 and optionally may be disposed at varying radial positions aboutneedle tube620.Anchor pushrod630 is translatably disposed withinanchor lumen626 ofneedle tube620 for deployment and adjustment ofanchor assemblies60, and bothneedle622 andanchor slot624 communicate withlumen626.Revolver640, comprising plurality ofchambers642, preferably is coupled to, or is integral with,flexible delivery tube610.Chambers642 communicate withlumen612 offlexible delivery tube610.
• Chambers642 preferably are pre-loaded with plurality ofanchor assemblies60. Furthermore,lumen626 ofneedle tube620 preferably is pre-loaded withfirst anchor assembly60a.Sutures39 extend proximally fromanchor assemblies60 toskives628, where sutures39 form knotted suture loops K that are reversibly constrained withinlumen626 ofneedle tube620 byanchor pushrod630, in order to facilitate adjustment of the length of suture disposed between the proximal and distal anchors of each assembly, as discussed previously.
• Suture39aoffirst anchor assembly60aextends proximally from firstproximal anchor64athroughanchor loading slot624 tofirst skive628a,where it forms first knotted suture loop Ka. In use,anchor pushrod630 may be used to deployfirst anchor assembly60afromlumen626 ofneedle tube620, for example, withdistal anchor62adisposed on the distal side of a tissue fold andproximal anchor64adisposed on the proximal side. After adjustment in the manner described previously,anchor pushrod630 may be retracted proximally to a position proximal offirst skive628a,thereby freeing first knotted suture loop fromlumen626. Proximal retraction ofanchor delivery system600 with respect tofirst anchor assembly60acompletely removessuture39afrom the delivery system, thereby completing deployment offirst anchor assembly60a.
• As discussed previously,chambers642 ofrevolver640 communicate withlumen612 offlexible delivery tube610. This facilitates loading ofsuccessive anchor assemblies60 withinneedle tube620 by longitudinally and radially aligning successive loadedchambers642 ofrevolver640 withanchor loading slot624 of the needle tube.Needle tube620 andrevolver640 optionally may be initially aligned such thatsecond anchor assembly60bdisposed inchamber642bdrops throughanchor loading slot624 intolumen626 ofanchor tube620 upon retraction ofanchor pushrod630 proximal ofanchor loading slot624, e.g., while releasing first knotted suture loop Ka fromlumen626. Subsequent loading of anchor assembly60c,etc., post-deployment, -adjustment and -release ofanchor assembly60b,may be achieved by rotatingneedle tube520 with respect torevolver540/delivery tube510, or vice versa.
• In this manner, plurality ofanchor assemblies60 may be delivered and deployed without necessitating reloading or removal ofanchor delivery system600 from the patient. InFIG. 27,revolver640 illustratively is shown with three loadedchambers642. However, any alternative number of chambers and anchor assemblies may be provided, as will be apparent to those of skill in the art. Additionally, optional motion limitation apparatus may be provided. Furthermore, detents, color-coding or other mechanisms may be provided to facilitate proper radial and longitudinal alignment ofdelivery tube610, needle tube620 (as well asanchor loading slot624 and skives628 of the needle tube),anchor pushrod630 and revolver640 (as well assuccessive chambers642 of the revolver) relative to one another.
• With reference now toFIGS. 28-34, additional plication apparatus for forming tissue folds is described.FIG. 28 illustrates an alternative embodiment ofapparatus200 ofFIG. 20.Apparatus200′ is adapted to simultaneously or sequentially form and approximate a plurality of tissue folds F within tissuewall W. Apparatus200′ may be used in conjunction with any of the anchors and anchor delivery systems described hereinabove, as well as with any applicable alternative anchors or systems, to secure the approximated tissue folds together. It is expected that approximating and securing a plurality of tissue folds will have substantial utility in performing a variety of medical treatments including, for example, gastric reduction.
• InFIG. 28,apparatus200′ comprises a plurality of articulate-able,flexible tubes177′, each with atissue grabbing assembly18′.Tubes177′ preferably are biased such that the tubes flare outward distal ofsheath650, thereby ensuring that the portions of tissue wall W plicated to form tissue folds F are separated by an appropriate distance prior to approximation, and that the tubes resiliently return to their flared position post-plication and release of tissuewall W. Tubes177′ preferably may be translated relative tosheath650. As seen inFIG. 28B,flexible tubes177′ articulate inward toward a longitudinal axis ofapparatus200′ in order to form and approximate tissue folds F. As will be apparent to those of skill in the art, a magnitude of the outward bias applied totubes177′ may be specified such that an appropriate initial separation distance L between the tissue grasping assemblies for a desired medical treatment is achieved. Furthermore, in order to reduce a delivery profile ofapparatus200′,flexible tubes177′ may be disposed within sheath650 (or another external sheath) during delivery.
• With reference toFIG. 29, an alternative embodiment ofapparatus10 ofFIG. 1 is described comprising backside stabilization. All plication apparatus described hereinabove comprise a distal region including a tissue grabbing assembly adapted to engage and stretch a portion of a tissue wall within a GI lumen at a first tissue contact point. A second tissue contact point then is established with the tissue wall at a location initially proximal of, or in line with, the first tissue contact point. The tissue engaged by the tissue grabbing assembly then is moved to a position proximal of the second tissue contact point to form a tissue fold, and an anchor assembly may be delivered across the tissue fold, e.g. across the muscularis and serosa layers of the tissue wall.
• Apparatus10′ ofFIG. 29 is a first embodiment of apparatus adapted to establish a third tissue contact point at another location initially proximal of, or in line with, the first tissue contact point; additional embodiments will be described hereinbelow. Upon movement of the tissue engaged by the tissue grabbing assembly to a position proximal of both the second and third tissue contact points, a tissue fold is formed with the second and third contact points on opposing sides of the fold. The second and third contact points provide both front and backside stabilization, respectively, of the tissue fold. When delivering an optional anchor assembly across the tissue fold from a vicinity of the second tissue contact point, backside stabilization at the third tissue contact point reduces backside tenting of tissue, thereby facilitating anchor delivery.
• InFIG. 29,apparatus10′ of the present invention comprisestorqueable catheter11′, which may be configured, for example, for insertion through a patient's mouth and esophagus into the patient's gastrointestinal lumen.Catheter11′ comprisesdistal region12′ having first and second interconnectedflexible tubes13 and14 extending therefrom.Tubes13 and14 are joined byhinge assembly20, andtissue grabbing assembly18 is disposed on the distal end offlexible tube13. The tissue grabbing assembly is coupled to a control wire (not shown) that extends throughtube13 to a proximal region ofcatheter11′ (not shown).
• Distal region12′ ofapparatus10′ is substantially the same asdistal region12 ofapparatus10 ofFIG. 1, except thatdistal region12′ further comprises selectivelydeployable backside stabilizer700.Backside stabilizer700 compriseswire loop710, which preferably is fabricated from a loop of shape memory material, e.g. Nitinol, coupled to controlwire720 that extends fromwire tube730. The proximal region ofcatheter11′ comprises actuators (not shown) in communication with the tissue grabbing assembly control wire andcontrol wire720 for actuating the tissue grabbing assembly and the backside stabilizer, respectively.
• Referring toFIGS. 30A-30E, a method of usingapparatus10′ ofFIG. 29 to form a backside stabilized tissue fold is described. InFIG. 30A,apparatus10′ is delivered to a treatment site throughdelivery sheath740 withwire loop710 compressed to a reduced delivery configuration within the delivery sheath. InFIG. 30B,distal region12′ ofcatheter11′ is advanced distal ofdelivery sheath740, such thatwire loop710 expands to a free-space configuration. InFIG. 30C,control wire720 ofbackside stabilizer700 is retracted proximally to retractwire loop710 to an intermediate ready position. InFIG. 30D, tissue fold F is formed at tissue wall W withdistal region12′, e.g., as described hereinabove with respect toFIG. 3.
• InFIG. 30E, tension is released fromcontrol wire720, andwire loop710 resiliently moves back towards its free-space configuration.Wire loop710 ofbackside stabilizer700 establishes a third tissue contact point on the backside of tissue fold F, thereby providing backside stabilization to the tissue fold. It is expected that backside stabilization/establishment of an opposing third tissue contact point will simplify delivery of an anchor assembly across the tissue fold while facilitating formation and securing of a serosa-to-serosa fold.
• As will be apparent to those of skill in the art, the size, length or diameter ofwire loop710 may be adjustable to facilitate backside stabilization of tissue folds of variable size. Furthermore,wire loop710 may be provided as a substantially stagnant loop, i.e. the loop may not be retractable viacontrol wire720. In such a configuration,wire loop710 would apply pressure to the tissue fold as it is formed, thereby facilitating formation of the fold in addition to providing stabilization.
• With reference now toFIG. 31, further alternative tissue folding apparatus comprising optional backside stabilization is described.Apparatus800 is adapted to linearly retract tissue at tissue wall W in order to form tissue fold F. The apparatus comprisescatheter810 havingtissue grabbing assembly18; such as described hereinabove and comprising a pair ofjaws28a,28bhaving sharpenedteeth33 arranged to rotate aboutpivot point29 between an open configuration and a closed configuration; coupled totube820 havingslot822.Control wire19 is disposed within the lumen oftube820 and extends fromtissue grabbing assembly18 to a proximal end of apparatus800 (not shown) for actuating the tissue grabbing assembly.Tissue grabbing assembly18 is configured to establish a first tissue contact point with tissue wall W and may be retracted proximally viatube820 to facilitate formation of tissue fold F.
• Apparatus800 further comprises frontside andbackside linkages830aand830b,respectively. Proximal regions of the linkages are pivotably and translatably disposed withinslot822 oftube820. A distal region offrontside linkage830ais pivotably coupled to anchordelivery tube840 for delivery of an anchor assembly across a tissue fold, as described previously, while a distal region ofbackside linkage830bis pivotably coupled tobackside stabilizer850.Anchor delivery tube840 andbackside stabilizer850 preferably are biased such that they substantially align with the longitudinal axis ofapparatus800 when not under stress. Such alignment may be achieved, for example, by forming the elements from spring tube, or by providing the elements with resilient spines, e.g. Nitinol spines.Tube840 andstabilizer850 are configured to establish second and third tissue contact points, respectively, at tissue wall W, thereby providing frontside and backside stabilization of a tissue fold formed at the wall, as described hereinabove.
• Referring again toFIG. 31, a method of usingapparatus800 to form tissue fold F at tissue wall W is described. InFIG. 31A,tissue grabbing assembly18 has been advanced to a vicinity of tissue wall W with the proximal ends of linkages830 disposed near the proximal end ofslot822 intube820.Tissue grabbing assembly18 is then actuated via retraction ofcontrol wire19 to grab tissue and establish the first tissue contact point. With tissue engaged, continued retraction ofcontrol wire19 causes proximal retraction oftube820 andassembly18 in a substantially linear fashion relative to linkages830, as seen inFIG. 31B.
• Astube820 is linearly retracted, linkages830 slidably translate withinslot822 of thetube820 until the proximal regions of the linkages contact a distal end ofslot822. As seen inFIG. 31C, further proximal retraction oftube820 beyond this bottoming-out point ofslot822 causes linkages830 to rotatably pivot at both their proximal and distal regions. This, in turn, causesanchor delivery tube840 andbackside stabilizer850 to rotate inwards and form the second and third tissue contact points, respectively, thereby forming frontside and backside-stabilized tissue fold F. Upon re-advancement oftube820,anchor delivery tube840 andbackside stabilizer850 resiliently realign with the longitudinal axis ofapparatus800.
• Previous plication apparatus described hereinabove require more complex motion than linear retraction on the part of the tissue grabbing assembly in order to form tissue fold F. It is expected that reducing movement of the tissue grabbing assembly during tissue folding to a linear motion will reduce a magnitude of working space required at a treatment site to achieve formation of the tissue fold. As will be apparent to those of skill in the art, as an alternative to linearly retractingtube820 relative to linkages830 in order to form tissue fold F, linkages830 may be linearly advanced relative totube820. Also,backside linkage830band backside stabilizer850 (as well as concomitant backside stabilization of tissue fold F) optionally may be omitted. Alternatively,backside stabilizer850 may comprise a second anchor delivery tube, e.g., for delivery of an anchor assembly across tissue fold F from the backside, for passage of all or part of an anchor assembly from frontsideanchor delivery tube840 to the backside stabilizer across the tissue fold, or for delivery of a multiple component anchor assembly having a first component deployable from the frontside anchor delivery tube and a second component deployable via the backside stabilizer. The first and second components optionally may be coupled together to form a composite anchor assembly. Additional configurations will be apparent to those of skill in the art.
• Furthermore, slot822 optionally may be omitted fromtube820, and the tube alternatively may be provided with proximal and distal stops disposed on the exterior of, or formed integral with, the tube near its distal end. In this arrangement, the proximal ends of linkages830 would be pivotably and translatably disposed about the exterior oftube820, such that the proximal and distal stops limit translation of the linkages relative to the tube. In both this arrangement and the arrangement ofFIG. 31,tube820 acts as a linear bearing about which linkages830 may travel.
• With reference now toFIG. 32, an alternative embodiment ofapparatus800 ofFIG. 31 is described.Apparatus800′ is substantially the same asapparatus800, except that linkages830 have been replaced with control wires830′, whileslot822 oftube820 has been replaced withskive822′ oftube820′. Additionally,anchor delivery tube840′ andbackside stabilizer850′ comprise optional pulley eyelets860aand860b,respectively, for routing of control wires830′. Control wires830′ are proximally coupled to controlwire19 oftissue grabbing assembly18 within the lumen oftube820′. Control wires830′ exit the lumen atskive822′ and extend distally through optional pulley eyelets860.Control wire830a′ is distally coupled to anchordelivery tube840′, whilecontrol wire830b′ is distally coupled tobackside stabilizer850′.
• A length of control wires830′ is specified such that retraction ofcontrol wire19 causes actuation oftissue grabbing assembly18 and retraction oftube820′, prior to control wires830′ being pulled taut. Once control wires830′ have been pulled taut, continued retraction ofcontrol wire19 causes control wires830′ to reversibly rotateanchor delivery tube840′ andbackside stabilizer850′ inward, thereby forming the second and third tissue contact points and forming frontside- and backside-stabilized tissue fold F at tissue wall W. As withapparatus800,backside stabilizer850′ (as well as associatedcontrol wire830b′) ofapparatus800′ optionally may be omitted.
• Referring toFIG. 33 further alternative tissue folding apparatus comprising optional backside stabilization is described.Apparatus900 comprisesouter tube910 havingdistal region912 with rigid or resilient frontside andbackside stabilizers914aand914b,respectively. When substantially rigid, stabilizers914 may be formed, for example, from a shaped stainless steel wire or rod. When resilient, the stabilizers may be formed, for example, from a wire or rod of shape memory material such as Nitinol or from a thinner wire or rod of stainless steel. The durometer of the material used to fabricate stabilizers914 may be specified to achieve a desired degree of rigidity or resiliency.
• Apparatus900 further comprisesinner tube920, which is coaxially and slidably disposed withinouter tube910.Tissue grabbing assembly922, coupled to a distal region ofinner tube910, compriseshelical coil924 having sharpeneddistal tip925.Helical coil924 is adapted to reversibly engage tissue by reversibly screwing the coil into the tissue in a manner similar to a wine corkscrew, and as demonstrated by arrows inFIG. 33A. As will be apparent to those of skill in the art, as an alternative or adjunct tohelical coil924,tissue grabbing assembly922 may comprise a jaw structure similar to that ofassembly18; likewise any of the previously described tissue folding apparatus optionally may comprise a tissue grabbing assembly having a helical coil. Additional tissue grabbing assemblies, per se known, will be apparent in view of this disclosure.
• FIG. 33 illustrate a method of forming a tissue fold withapparatus900. InFIG. 33A,tissue grabbing assembly922 is advanced distal of stabilizers914 to engage tissue at tissue wall W at a first tissue contact point.Helical coil924 is screwed into the tissue, andinner tube920 is then retracted relative toouter tube910, and/or the outer tube is advanced relative to the inner tube, such that tissue engaged byassembly922 is pulled proximal of stabilizers914, as seen inFIG. 9B. Stabilizers914 contact the tissue at second and third contact points, and form frontside- and backside-stabilized tissue fold F. When rigid, a cross-sectional width of tissue fold F may be specified by a separation distance between the frontside and backside stabilizers. When resilient, the stabilizers may bow outward to facilitate formation of the tissue fold by decreasing a pulling force required bycoil924 to form the fold, as well as by reducing a risk of the coil detaching from, or tearing through, the tissue during fold formation.
• As will be apparent to those of skill in the art, one ofstabilizer914aandstabilizer914boptionally may be omitted when only a second tissue contact point is required. Additionally,apparatus900 may be used in conjunction with an anchor delivery system, such as those described previously; the anchor delivery system optionally may provide the third tissue contact point. Also, one or both of stabilizers914 may be extendable/retractable relative todistal region912 ofouter tube910 ofapparatus900. Likewise, the stabilizers may be sizable in vivo to facilitate formation of a tissue fold of specified magnitude.
• With reference now toFIG. 34, another embodiment of plication apparatus comprising backside stabilization is described. In contrast to previously described apparatus,apparatus950 achieves backside stabilization of a tissue fold via tissue contact over an arcuate segment, as opposed to at discrete points or along a line. InFIG. 34, full 360° radial contact around the fold is established; however, as will be apparent to those of skill in the art, contact alternatively may be established at one or more locations over one or more arcuate segments of less than 360°.
• Apparatus950 comprisesinner tube960 and coaxially disposedouter tube970.Inner tube960 comprisestissue grabbing assembly18 coupled to a distal of the tube.Apparatus950 further comprises braidedmesh980 havingproximal end982 coupled to a distal end ofouter tube970, anddistal end984 coupled toinner tube960 proximal oftissue grabbing assembly18.Braided mesh980 preferably is fabricated from polymer or metal wires. Upon advancement ofouter tube970 relative toinner tube960, the mesh may be everted, e.g. over a tissue fold, to provide frontside and backside stabilization of a fold via arcuate contact. As will be apparent,apparatus950 may be used in conjunction with an anchor delivery system to secure a stabilized tissue fold.
• FIG. 34 illustrate a method of usingapparatus950 to form a stabilized tissue fold. InFIG. 34A,tissue grabbing assembly18 engages tissue wall W at a first tissue contact point. InFIG. 34B, with tissue engaged byassembly18,inner tube960 is retracted relative toouter tube970 and/orouter tube970 is advanced relative toinner tube980, such thatproximal end982 is advanced distal ofdistal end984 ofbraided mesh980. The braided mesh everts about tissue fold F, thereby providing frontside and backside stabilization to the tissue fold via contact over a full 360° radial segment (braidedmesh980 shown in section inFIG. 34B).
• FIGS. 29-34 have illustrated exemplary plication apparatus comprising optional elements for backside stabilizing tissue folds formed with the apparatus. As will be apparent to those of skill in the art, backside stabilization elements optionally may also be provided with any other plication apparatus of the present invention. Furthermore, backside stabilization elements may be provided with any anchor delivery system, e.g., in order to reduce tissue tenting during deployment of an anchor assembly across a tissue fold.
• With reference now toFIGS. 35-39, an embodiment of a shape-lockable guide for use with tools of the present invention is described. Shape-lockable guides have been described previously in Applicant's co-pending U.S. patent application Ser. No. 10/173,203, filed Jun. 13, 2002, which is incorporated herein by reference in its entirety and from which the present invention claims priority. As discussed hereinabove, a significant indication for use of the tissue grabbing assemblies, plication apparatus, anchor delivery systems and anchor assemblies of the present invention is within a patient's gastrointestinal (“GI”) lumen. However, the GI lumen varies significantly in geometry and material properties along its length, and it is expected that properly positioning, as well as visualizing, endoluminal tools of the present invention at any desired location within the GI lumen will present significant challenges. Transmitting forces and torques to the tools over substantial separation distances between a medical practitioner and the working ends of the tools within the GI lumen presents additional challenges. It therefore would be nice to provide guide apparatus capable of providing exposure or targeting, stability, and flexibility to tools of the present invention when disposed within a patient.
• Apparatus1000 ofFIGS. 35-39 addresses these challenges by facilitating placement of a diagnostic instrument, such as an endoscope, e.g., a colonoscope or gastroscope; and/or a therapeutic instrument, such as those described hereinabove; through the tortuous or unpredictably supported anatomy of a hollow body organ, such as the colon, esophagus and/or stomach; while reducing a risk of distending or injuring the organ.Apparatus1000 permits such instruments to be readily advanced into the patient's tortuous or unpredictably supported anatomy by selectively shape-fixing an overtube portion of the apparatus, while also preventing tissue from being captured or pinched between the overtube and the instrument(s). Althoughapparatus1000 illustratively comprises an overtube, it should be understood thatapparatus1000 alternatively may comprise a selectively rigidizable, shape-fixing or shape-locking guide wire or inner conduit, over which diagnostic or therapeutic instruments may be advanced.
• Referring now toFIG. 35,apparatus1000 of the present invention is described.Apparatus1000 compriseshandle1001, overtube1002, anddistal region1003 havingatraumatic tip1004.Handle1001 includeslumen1005 that extends from Toughy-Borst valve1006 throughovertube1002,distal region1003 andatraumatic tip1004.Lumen1005 is configured to facilitate passage of a standard commercially available endoscope, such asendoscope1100 having steerable distal tip1101 (seeFIG. 40), and/or a therapeutic device of the present invention, e.g. a tissue grabbing assembly, plication apparatus, an anchor delivery system, or an anchor assembly, therethrough. Althoughapparatus1000 illustratively comprises a single lumen, multiple lumens optionally may be provided for passage of multiple diagnostic and/or therapeutic instruments. Toughy-Borst valve1006 may be actuated to releasably lock instrument(s) toapparatus1000 when the instrument(s) are inserted withinlumen1005. As described hereinafter, overtube1002 is configured so that it can be selectively transitioned between a flexible state and a rigid, shape-fixed state by actuator1007 disposed onhandle1001.
• InFIG. 36, an illustrative embodiment ofovertube1002 comprises a multiplicity ofnestable elements1010. For purposes of illustration,nestable elements1010 are shown spaced-apart, but it should be understood thatelements1010 are disposed so that theiradjacent surfaces1011 and1012 coact. Each ofnestable elements1010 hascentral bore1013 to accommodate diagnostic and therapeutic instruments, and preferably three or more tension wire bores1015. When assembled as shown inFIG. 35,nestable elements1010 are fastened withadjacent surfaces1011 and1012 disposed in a coacting fashion by a plurality oftension wires1016 that extend through tension wire bores1015.
• In a preferred embodiment,adjacent surfaces1011 and1012 of eachnestable element1010 are contoured to mate with the next adjacent element, so that whentension wires1016 are relaxed, surfaces1011 and1012 can rotate relative to one another.Tension wires1016 are fixedly connected to the distal end ofovertube1002 at their distal ends and to a tensioning mechanism disposed withinhandle1001 at their proximal ends. When actuated byactuator1007,tension wires1016 impose a load that clampsadjacent surfaces1011 and1012 ofnestable elements1010 together at the current relative orientation, thereby fixing the shape ofovertube1002.
• When the load intension wires1016 is released,tension wires1016 provide for relative angular movement betweennestable elements1010. This in turn renders overtube1002 sufficiently flexible to negotiate a tortuous path or unpredictably supported anatomy through, for example, any region of a patient's GI lumen, such as the colon, esophagus and/or stomach. When the tensioning mechanism is actuated, however,tension wires1016 are retracted proximally to apply a clamping load to the nestable elements. This load prevents further relative movement betweenadjacent elements1010 and stiffens overtube1002, so that any distally directed force applied to instruments withinlumen1005 causes the working ends of the instruments to advance further into the GI lumen, rather than cause overtube1002 to bear against the wall of the lumen or lose its spatial orientation within an unpredictably supported space. The shape-fixed overtube absorbs and distributes vector forces, shielding the GI lumen.
• Referring now toFIG. 37, an illustrative embodiment ofdistal region1003 andatraumatic tip1004 is described.Distal region1003 comprises flexible, kink-resistant coil1021 encapsulated inflexible layer1022.Layer1022 preferably comprises a soft elastomeric and hydrophilic coated material, such as silicon or synthetic rubber, and extends throughbores1013 ofnestable elements1010 to formliner1023 forlumen1005.Layer1022 extends to handle1001 at the proximal end, and at the distal end terminates inenlarged section1024 that formsatraumatic tip1004.
• Layer1022 preferably joins with or is integrally formed with flexibleelastomeric cover1025 which encapsulatesnestable elements1010 inannular chamber1026.Cover1025 provides a relatively smooth outer surface forovertube1002, and prevents tissue from being captured or pinched during relative rotation of adjacentnestable elements1010.
• In accordance with one aspect of the present invention,endoscope1100 may be positioned with itsdistal tip1101 disposed indistal region1003, so that deflection of steerabledistal tip1101 imparts an angular deflection todistal region1003 andatraumatic tip1004. To ensure that there is no gross relative motion betweenendoscope1100 or other instruments withinlumen1005 andapparatus1000, Toughy-Borst valve1006 is tightened to engageapparatus1000 to the endoscope/instruments. In this manner, the instrument(s) anddistal region1003 may be simultaneously advanced through the colon, with the distal tip ofendoscope1100 providing a steering capability toapparatus1000.Apparatus1000 therefore may be advantageously advanced together with instruments disposed withinlumen1005 when overtube1002 is in the flexible state, reducing relative motion betweenapparatus1000 and such instruments to those instances where overtube1002 must be shape-locked to prevent distension or to maintaindistal region1003 orientation with the GI lumen.
• Still referring toFIG. 37,terminations1027 of tension wires are described.Terminations1027 illustratively comprise balls welded or molded onto the ends oftension wires1016 that ensure the tension wires cannot be pulled through tension wire bores1015 of the distalmost nestableelement1010. This ensures that the nestable elements cannot come loose when overtube1002 is disposed within a patient.
• Alternatively,terminations1027 may comprise knots formed in the ends oftension wires1016, or any suitable fastener that prevents the tension wires from being drawn through the tension wire bores of the distal-most nestable element. Advantageously,cover1025 provides additional assurance that all ofnestable elements1010 can be safely retrieved from a patient's colon in the unlikely event of a tension wire failure.
• Referring now toFIGS. 35 and 38,tension wires1016 within overtube1002,liner1023 andlumen1005 extend fromdistal region1003, throughovertube1002, and to handle1001. Withinhandle1001, eachtension wire1016 passes throughwire lock release1031 fixedly attached to handle1001, andwire lock1032 disposed onslide block1033. Eachtension wire1016 terminates atwire tension spring1034, which maintainstension wires1016 in light tension even when overtube1002 is in the flexible state. The degree of tension provided by wire tension springs1034 is not sufficient to clamp adjacentnestable elements1010 together, but on the other hand does not let gaps form between adjacent nestable elements, and helps to manage the tension wire take up or slack asovertube1002 makes various bends.
• Slide block1033 is keyed to slide alongrail1035 disposed betweenlimit blocks1036 and1037, and comprises a rigid block having a bore through whichrail1035 extends and an additional number of bores as required for the number oftension wires1016 employed.Rack gear1038 is fixedly coupled to slideblock1033.Rack1038 mates withpinion gear1039, which is in turn driven bybi-directional pawl1040 coupled toactuator1007.Pinion gear1039 may be selectively engaged by eitherprong1041 or1042 ofbidirectional pawl1040, depending upon the position ofselector switch1043.
• Ifprong1041 is selected to be engaged withpinion gear1039, a squeezing action applied toactuator1007,illustratively hand grip1044, causes rack1033 to move in the D direction inFIG. 38, thereby applying tension totension wires1016. Repeated actuation ofhand grip1044 causesslide block1033 to move progressively further in direction D, thereby applying an increasing clamping load onnestable elements1010. Any slack lengths oftension wires1016 extending belowslide block1033 are taken up by wire tension springs1034. As discussed in greater detail below with respect toFIG. 39,wire locks1032, which are affixed to slideblock1033, engage and retracttension wires1016 concurrently with movement ofslide block1033 in the D direction.
• Ifprong1042 is instead chosen byselector switch1043 to engagepinion gear1039, repeated actuation ofhand grip1044 causesslide block1033 to translate in direction U, thereby relaxing the tensile load applied bytension wires1016 tonestable elements1010. Repeated actuation ofhand grip1044 causesslide block1033 to advance in direction U untilwire lock releases1031 engagewire locks1032, releasing all tension fromtension wires1016 except that provided by wire tension springs1034. This action permits the clamping forces imposed onnestable elements1010 to be progressively reduced and render overtube1002 progressively move flexible, until whenwire lock releases1031 engagewire locks1032, the overtube is returned to its most flexible state.
• Referring toFIG. 39,wire lock1032 andlock release1031 are described in greater detail.Wire lock1032 includesjaws1045 disposed withincollet1046.Collet1046 includes a taperedconical bore1047.Jaws1045 have rampedexterior surfaces1048 andteeth1049, and are biased against the surface formed by the tapered conical bore by springs70.Teeth1049 are configured to engagetension wire1016 under the bias force of springs70. Whenslide block1033 is moved in direction D (seeFIG. 38),jaws1045 engage and grasptension wire1016 and retract the tension wire in direction D.
• To disengageteeth1049 fromtension wire1016, e.g., when it is desired to allow overtube1002 to return to a flexible state,slide block1033 is actuated as described previously to move in direction U. Further actuation ofslide block1033 towardslimit block1036 andwire lock release1031 causeswire lock release1031 to extend into taperedconical bore1047 and pushjaws1045 backward against the bias of springs70. Oncetension wires1016 are freed fromjaws1045, overtube1002 returns to its most flexible state.
• InFIGS. 35-39,apparatus1000 has been described as having a flexible state and rigid state. However, it should be understood thatapparatus1000 optionally may comprise one or more intermediary states wherein overtube1002 is only partially flexible or only partially rigid. Furthermore, overtube1002 optionally may comprise one or more sections of varied rigidity or flexibility in either the flexible or the rigid state, or both, as compared to one or more other sections of the overtube. For example, at least one section of the overtube may remain in the flexible state upon transition of the overtube to the rigid state. Alternatively, at least one section of the overtube may comprise varied rigidity relative to a different section of the overtube when the overtube is disposed in the rigid state. As yet another alternative, at least one section of the overtube may comprise varied flexibility relative to a different section of the overtube when the overtube is disposed in the flexible state. Additional configurations will be apparent to those of skill in the art.
• It should be understood thatapparatus1000 optionally may be provided with steering capabilities in addition to locking capabilities, in order to properly positionapparatus1000 within a GI lumen, e.g. prior to locking the overtube in a desired orientation. Such steering capabilities may be achieved, for example, using tensioning or stiffening wires, per se known. Additional steering techniques will be apparent to those of skill in the art.
• As an alternative, or in addition, to advancing diagnostic and/or therapeutic instruments through one or more lumens ofapparatus1000, such instruments optionally may be coupled toapparatus1000. For example, an endoscope, a tissue grabbing assembly, plication apparatus and/or an anchor delivery system in accordance with the present invention, may be coupled todistal region1003 ofapparatus1000. Alternatively, such instruments may be telescopically disposed and advanced from withindistal region1003. Coupling instruments or tools to a shape-lockable guide is described in more detail, for example, in Applicant's co-pending U.S. patent application Ser. No. 10/458,060, filed Jun. 9, 2003, which is incorporated herein by reference in its entirety and from which the present invention claims priority. Additional configurations will be apparent to those of skill in the art.
• With reference now toFIG. 40, in conjunction withFIG. 41, a method of performing endoluminal gastric reduction is described utilizing a system of tools illustratively comprising commerciallyavailable gastroscope1100,plication apparatus10 ofFIGS. 1-3,anchor delivery system250 ofFIG. 21 loaded withanchor assembly60 ofFIG. 7, and shape-lockable apparatus1000 ofFIGS. 35-39. Gastric reduction is a technique for reducing a patient's appetite and/or ability to ingest food by reducing a volume of the stomach through which food may pass. Endoluminal gastric reduction in accordance with the present invention entails partitioning the stomach into first and second chambers, and more specifically into a small lumen or pouch and a larger chamber, over at least a portion of the stomach.
• The lumen/pouch preferably has a volume of approximately 10-50 cm3, and even more preferably a volume of approximately 15 cm3, and is positioned near and inferior to the patient's gastroesophageal junction. Ingested food may only pass through the small lumen over the partitioned portion of the stomach. The lumen preferably is formed by approximating opposing anterior and posterior segments of the patient's stomach wall over a length or arc of the wall near and inferior to the gastroesophageal junction.
• As illustrated inFIGS. 40 and 41, endoscopic gastric reduction may be achieved by endoscopically forming, approximating and securing a plurality of tissue folds in a first plane within a patient's stomach, then endoscopically forming, approximating and securing at least one additional plurality of tissue folds in at least one substantially parallel plane within the patient's stomach. The first plurality of tissue folds and the at least one additional plurality of tissue folds may be attached or detached from one another. Each plurality of folds preferably comprises one or more tissue folds from opposing anterior and posterior segments of the stomach near and inferior to the gastroesophageal junction.
• More, specifically, endoscopic gastric reduction may be achieved by advancing an overtube through a patient's esophagus into the patient's stomach while the overtube is disposed in a flexible state, then transitioning the overtube to a rigid state in a desired orientation within the patient's stomach. A plication device, either coupled to the overtube or advanced therethrough, may then be used to form the plurality of tissue folds, while an anchor delivery system may be used to approximate and/or secure the tissue folds, thereby partitioning the patient's stomach.
• InFIG. 40, overtube1002 of shape-lockable apparatus1000 illustratively comprises first andsecond lumens1005aand1005bfor passage ofgastroscope1100 andplication apparatus10/anchor delivery system250, respectively. InFIG. 40A, optionalthin wall sheath2000 is disposed within a patient's gastrointestinal lumen through the patient's mouth, into esophagus E, past the gastroesophageal junction GE, and into the patient's stomach S. Shape-lockable overtube1002 ofapparatus1000 is advanced throughsheath2000 into stomach S while disposed in the flexible state.Sheath2000 provides a barrier betweenovertube1002 and esophagus E, which may facilitate increased maneuverability ofapparatus1000 by protecting the esophagus during optional torqueing, translation and/or articulation ofovertube1002.
• InFIG. 40A,gastroscope1100 illustratively has been advanced throughlumen1005aofovertube1002 pastdistal region1003 while the overtube is disposed in the flexible state. As will be apparent to those of skill in the art, a visualization element alternatively or additionally may be coupled toovertube1002; multiple point visualization may facilitate complex procedures and/or enable triangulation for deployment of anchor assemblies across tissue folds. Furthermore,plication apparatus10 andanchor delivery system250 optionally may be coupled to the overtube or may be advanced through the overtube while the tube is disposed in the flexible state.
• InFIG. 40B, overtube1002 is articulated to an orientation wherebydistal region1003 facilitates engagement of tissue near and inferior to the patient's gastroesophageal junction GE. Such articulation may be achieved, for example, by actuating steerabledistal tip1101 ofgastroscope1100. Alternatively,apparatus1000 may comprise steering features. As yet another alternative, a steering tool, such as a shaped wire, may be advanced throughsecond lumen1005bto properly orient the overtube. Furtherstill, the overtube may comprise a pre-formed flexible shape whereby the overtube assumes an arcuate configuration, and a rigid wire may be reversibly disposed withsecond lumen1005bofovertube1002 in order to straighten the overtube during insertion through esophagus E; upon positioning ofdistal region1003 ofapparatus1000 within stomach S, the wire may be removed from the lumen, such that overtube1002 re-assumes its pre-formed shape. As yet another alternative,plication apparatus10 and/oranchor delivery system250 may comprise steering features and may be advanced through the second lumen to steer the overtube into position.
• Withapparatus1000 disposed in the desired configuration or orientation, the apparatus is reversibly shape-locked to a rigid state as described previously, such that the apparatus maintains its position within the stomach. Preferably, the articulated portion ofapparatus1000 traverses an arc of substantially continuous radius of curvature in the shape-locked configuration, thereby reducing a magnitude of forces required to advance and retract instruments throughovertube1002. In a preferred embodiment, the arc traverses approximately 270° and has a radius of curvature between about 5 and 10 cm, and, even more preferably, approximately 7-8 cm. By retroflexing about 270°,distal region1003 ofapparatus1000 is directed back towards the body ofovertube1002 near and inferior to gastroesophageal junction GE.
• Plication apparatus10 andanchor delivery system250 are advanced throughsecond lumen1005bofovertube1002 distal of distal region1003 (alternatively, the plication apparatus and anchor delivery system may be coupled to the overtube). As seen inFIG. 40C, e.g. under visualization provided bygastroscope1100, tissue is engaged within stomach S usingtissue grabbing assembly18. Tissue fold F is formed, for example, as described previously with respect toFIG. 3.Anchor assembly60 then is deployed across the tissue fold via anchor delivery system-250 and is adjusted to secure the fold, for example, as described hereinabove with respect toFIG. 21.
• As discussed previously and seen inFIG. 41, in order to achieve endoluminal gastric reduction, opposing anterior An and posterior Po surfaces of stomach S are drawn together to partition the stomach into first lumen or pouch P and second larger chamber C. As seen inFIG. 41C, in order to achieve such partitioning, a plurality of folds is formed on the opposing surfaces in a first plane P1. The opposing folds are connected bysuture39 or by other means and are approximated, for example, by reducing a length of suture disposed between the opposing surfaces, to partition the stomach as inFIG. 41B.
• Optionally, at least one additional plurality of folds may be formed on the opposing anterior An and posterior Po surfaces in at least one additional plane that is substantially parallel to first plane P1.FIGS. 40D and 41C comprise optional additional pluralities of tissue folds in second and third planes P2 and P3. In effect, an anterior ridge AR of tissue folds is formed, and an opposing posterior ridge PR of tissue folds is formed. These additional pluralities of tissue folds may be attached to the first plurality of tissue folds, as inFIG. 41C, or may be unattached. Upon approximation of the tissue folds, for example, via cinching ofsuture39, pouch P is formed, and endoluminal gastric reduction is achieved.
• The number of planes in which pluralities of tissue folds are formed may be specified based on a preferred longitudinal spacing of anchor assemblies and/or based upon a desired length of pouch P. The desired length L may be specified based on a desired volume V of pouch P and a diameter D of pouch P, according to the following equation:
  L=4V/(πD²)   (1)
  For example, overtube1002 preferably has an outer diameter of approximately 1.6 cm. Thus, the diameter of pouch P must be at least 1.6 cm, so that the overtube may pass through the pouch. Assuming a pouch diameter of approximately 1.6 cm, and in order to provide the pouch with a volume of about 15 cm3, a length of pouch P should be about 7.5 cm.
• Referring again toFIG. 40C, in order to form, secure and approximate tissue folds on opposing anterior An and posterior Po surfaces of stomach S, as well as in multiple planes P, overtube1002 preferably comprises multiple degrees of freedom. Arrows inFIG. 40C describe illustrative directions in whichapparatus1000 may be maneuvered to re-orient or reconfigureovertube1002. Specifically,apparatus1000 may be translated relative to esophagus E andsheath2000, as described by arrow Tr. Furthermore,apparatus1000 may be torqued, as described by arrow To. Furtherstill, the apparatus may be articulated, as described by arrow ARt. As will be apparent, additional or alternative degrees of freedom optionally may be provided.
• As an example, a medical practitioner translating ortorqueing handle1001 ofapparatus1000 from external to the patient may achieve translation and torqueing ofovertube1002. Articulation may be achieved by a number of means, such as steering features provided within overtube1002, e.g. a tensioning wire, or by temporarily returning overtube1002 to the flexible state, actuatingsteerable end1101 ofgastroscope1100 to articulate overtube1002 to a desired configuration, then once again shape-locking overtube1002 to the rigid state. Combinations of torqueing, translation and articulation may be used to position overtube1002 in any desired configuration.
• InFIG. 40D, by repositioning overtube1002, re-loadinganchor delivery system250, andre-actuating plication apparatus10 andanchor delivery system250, tissue folds have been formed, secured and approximated on opposing surfaces in multiple planes, thereby forming pouch P and chamber C withinstomach S. Overtube1002 has been transitioned back to the flexible state, and all instruments advanced through the overtube have been removed fromapparatus1000.Overtube1002 andoptional sheath2000 now may be removed from stomach S and esophagus E through pouch P, thereby completing endoluminal gastric reduction.
• With reference now toFIG. 42, a method of treating gastroesophageal reflux disease (“GERD”) using the system of tools described with respect toFIG. 40 is provided.Apparatus1000 is advanced through a patient's esophagus E withovertube1002 disposed in a flexible state. Once again,optional sheath2000 may be provided between esophagus E andapparatus1000. The apparatus is then manipulated, for example, as described hereinabove, into a configuration enabling access to tissue in a vicinity of the patient's gastroesophageal junction GE.Overtube1002 is then shape-locked to a rigid state, as seen inFIG. 42A.
• InFIG. 42B, plication apparatus10 (either advanced through or coupled to apparatus1000) is used to form tissue fold F₁on a first side of gastroesophageal junction GE.Anchor assembly60, which is deployed and adjusted viaanchor delivery system250, secures the tissue fold. Visualization of the procedure is achieved, for example, viagastroscope1100.
• Tissue fold F₁provides a flap that reduces reflux of acid or other stomach materials into esophagus E. In patients with more serious conditions, it may be necessary to provide one or more additional folds around gastroesophageal junction GE. For example,apparatus1000 may be repositioned,anchor delivery system250 reloaded, and opposing fold F₂formed, as inFIG. 42C. After a desired pressure differential has been established across gastroesophageal junction GE, overtube1002 may be returned to the flexible state, andapparatus1000, as well as any instruments advanced therethrough or coupled thereto, may be removed from the patient, thereby providing endoluminal treatment of gastroesophageal reflux disease. Optionally, first and second pressure sensors Fri and Pr2 may be provided along the length ofapparatus1000 to measure the pressure differential across gastroesophageal junction GE, as seen inFIG. 42B. In use, first pressure sensor Fri may be positioned distal of the junction within the patient's stomach S, while second pressure sensor Pr2 is disposed proximal of the junction within the patient's esophagus E. Additional or alternative sensors will be apparent to those of skill in the art.
• With reference now toFIG. 43, an alternative method for achieving endoluminal gastric reduction or remodeling is described. Inamed Corporation of Santa Barbara, Calif., markets the BioEnterics® LAP-BAND® System, which consists of an inflatable silicone band that is laparoscopically placed within a patient's abdomen. The band is fastened around the upper stomach, giving the stomach an hourglass profile and creating a tiny stomach pouch that limits and controls an amount of food the patient can ingest. It also creates a small outlet that slows the emptying process into the stomach and the intestines. According to the company's website, patients using the system experience an earlier sensation of fullness and are satisfied with smaller amounts of food, which results in weight loss.
• A significant drawback of the BioEnterics® LAP BAND® System is that a laparascopic incision must be made within the patient's abdomen in order to place the device. Applicant's co-pending U.S. patent application Ser. No. 10/288,619, which is incorporated herein by reference in its entirety, and from which the present application claims priority, describes endoluminal methods and apparatus for providing the stomach with an hourglass profile to facilitate weight loss, thereby mitigating a need for laparascopic incisions. InFIG. 43, a system of tools of the present invention is used to endoluminally achieve such gastric reduction or remodeling via plicated tissue folds. In the method ofFIG. 43, only suture is disposed on the exterior of the stomach post-reduction/remodeling.
• InFIG. 43A, a plurality of tissue folds F have been formed around the circumference of stomach S within an upper portion of the stomach via a system of tools comprisingplication apparatus10, a plurality ofanchor assemblies60 interconnected bysuture39, multi-fireanchor delivery system500, shape-lockable apparatus1000 andgastroscope1100. InFIG. 43B, the interconnected anchor assemblies have been cinched together, thereby approximating the plurality of tissue folds F, and endoluminally providing stomach S with an hourglass profile. The system of tools may then be removed from the patient, thereby completing endoluminal reduction or remodeling of stomach S.
• InFIGS. 40-42, as an alternative to usinganchor delivery system250 ofFIG. 21, a multi-fire anchor delivery system, such asanchor delivery system500,500′ or600 ofFIGS. 25-27 (loaded, for example, withmultiple anchor assemblies60 ofFIG. 7), may be used so as to omit a need to remove and reload all or a portion of the anchor delivery system from the patient's GI lumen in order to deploy and secure multiple anchor assemblies across one or more tissue folds. Furthermore, although the methods ofFIGS. 40-43 have illustratively been described with reference to a system of tools comprisingplication apparatus10,anchor assembly60, anchor delivery system250 (delivery system500 inFIG. 43), shape-lockable apparatus1000 andgastroscope1100, any combination of diagnostic or therapeutic tools/instruments in accordance with the present invention may be utilized, including, for example, alternative plication apparatus, anchor assemblies, anchor delivery systems and shape-lockable apparatus described previously. Furtherstill, although the visualization element described inFIGS. 40-43 comprises an endoscope or gastroscope, it should be understood that any other alternative or additional methods or apparatus for visualizing a medical procedure may be provided, including, but not limited to, magnetic resonance imaging, ultrasound imaging, optical coherence tomography imaging, fluoroscopic imaging, and combinations thereof. Also, although the system of tools have illustratively been described as advanced through shape-lockable apparatus1000, it should be understood that any or all of the tools alternatively or additionally may be coupled toapparatus1000, for example, todistal region1003 ofapparatus1000.
• FIGS. 40-43 have presented methods of using apparatus of the present invention to perform endoluminal gastric reduction and treatment of GERD. Alternative methods for performing these medical procedures using apparatus of the present invention will be apparent to those of skill in the art. For example, U.S. Pat. No. 6,540,789 to Silvermann et al., which is incorporated herein by reference, describes a method for performing gastric reduction by injecting bulking agents into a patient's stomach at a plurality of locations, thereby reducing a volume of the stomach. Apparatus of the present invention may be used to reduce the volume of a patient's stomach by forming a plurality of secured tissue folds within the stomach. The tissue folds may be formed, for example, at a plurality of randomly selected locations. Alternatively, apparatus of the present invention may be used to perform gastric reduction via placement and/or sizing of an implantable stoma within the stomach. As yet another example, marking devices may be provided with apparatus of the present invention in order to map out locations for formation of tissue folds, e.g., to achieve gastric reduction. Additional methods will be apparent.
• Apparatus of the present invention should in no way be construed as limited to treatment of GERD or morbid obesity. Rather, a variety of other medical procedures—both diagnostic and therapeutic, or a combination thereof—may be performed within a patient's gastrointestinal lumen or other body cavities or organs, including hollow, tortuous and/or unpredictably supported body cavities, using tools and instruments of the present invention. These include, but are not limited to, endoscopic retrograde cholangiopancreatography (“ERCP”), intubation of the bile duct, upper or lower gastrointestinal endoscopy, colonoscopy, flexible sigmoidoscopy, esophageal dilatation, anastomosis, liver biopsy, esophageal manometry, esophageal pH, cholecystectomy, enteroscopy, resection of lesions or early cancers, treatment of bleeding sites, trans-esophageal microsurgery, trans-anal microsurgery, and combinations thereof. Additional procedures will be apparent to those of skill in the art.
• With reference toFIG. 44, an exemplary method of resecting a lesion or early cancer, e.g. within a patient's gastrointestinal tract, using apparatus of the present invention is described. InFIG. 44, system oftools3000 comprises shape-lockable overtube1000 havingsuction plicator1500 coupled to its distal end.System3000 further comprisesendoscope1100 andtool delivery tube1600 disposed withinlumen1005 ofovertube1000.Tool delivery tube1600 optionally may comprisedelivery tube252 ofanchor delivery system250, as described hereinbelow with respect toFIG. 45, or may comprise the delivery tube of any alternative anchor delivery system described previously. Furthermore,tube1600 may be coupled to overtube1000 or may advanceable relative to the overtube.
• Suction plicator1500 comprisesside aperture1510 to facilitate side-suction plication of tissue.Plicator1500 additionally or alternatively may comprise one or more apertures at its distal end (not shown) to facilitate end-suction plication of tissue.Plicator1500 and overtube1000 preferably are sealed along their lengths, such that suction may be drawn through the overtube and plicator, e.g., via a suction pump (not shown) coupled to a proximal region ofovertube1000 external to the patient.
• Advantageously, as compared to previously-known suction plication apparatus, shape-lockable overtube1000 allows system oftools3000 to be positioned at a treatment site while the overtube is disposed in a flexible state.Overtube1000 then optionally may be transitioned to a rigid state prior to drawing of suction throughplicator1500. In this manner,system3000 may be directed to, and maintained at, a treatment site during a medical procedure.
• InFIG. 44, shape-lockable overtube1000 has been endoscopically advanced, e.g., through a patient's esophagus or colon, under endoscopic visualization provided byendoscope1100, to a vicinity of lesion or early cancer C along tissue wall W, while the overtube was disposed in a flexible state.Overtube1000 alternatively may be advanced laparoscopically, e.g. through a trocar. The overtube preferably is then transitioned to a rigid state in a configuration enabling access, e.g. luminal access, to the lesion or early cancer.
• Suction is drawn throughovertube1000 andsuction plicator1500 to urge tissue in the vicinity of lesion/early cancer C throughside aperture1510 and intolumen1005 ofovertube1000, thereby forming tissue fold F. As can be verified by endoscopic visualization, lesion or cancer C resides on the folded tissue. The lesion, polyp, cancer, etc. then may be removed via cutting apparatus, such as snare orresection loop1700 advanced throughtool delivery tube1600. As will be apparent to those of skill in the art, alternative plication apparatus in accordance with the present invention may be used to resect lesion C.
• With reference now toFIG. 45, an exemplary method for endoscopically treating a bleeding site, e.g. within a patient's gastrointestinal tract, is described. InFIG. 45, system oftools3000′ is substantially the same assystem3000 ofFIG. 44, except thattool delivery tube1600′ illustratively comprisesdelivery tube252 of anchor delivery system of250, andresection loop1700 illustratively has been replaced withanchor delivery system250 andanchor assembly60 for securing tissue folds drawn through side-aperture1510 ofsuction plicator1500.System3000′ has been positioned, and tissue fold F has been formed, utilizing the techniques described hereinabove with respect toFIG. 44, such that bleeding site B resides on folded tissue F.Anchor delivery system250 havingneedle260 is then actuated in the manner described previously to deploy and adjustanchor assembly60 and secure tissue fold F, thereby sealing and precluding additional bleeding from bleeding site B.
• As will be apparent to those of skill in the art, alternative plication apparatus and/or anchor delivery systems in accordance with the present invention may be used to treat bleeding site B. Furthermore, althoughtool systems3000 and3000′ ofFIGS. 44 and 45, respectively, have illustratively been described for use in resecting lesions and/or treating bleeding sites, these systems alternatively or additionally may be used for any other applicable medical procedure, including, but not limited to, those described previously, such as gastric reduction and treatment of gastroesophageal reflux disease.
• Although preferred illustrative embodiments of the present invention are described hereinabove, it will be apparent to those skilled in the art that various changes and modifications may be made thereto without departing from the invention. It is intended in the appended claims to cover all such changes and modifications that fall within the true spirit and scope of the invention.

Claims (56)

1. An endoscopic system for suturing tissue, comprising:

a needle adapted to suture an area of tissue, the needle being removable from a distal end of an endoscopic device;

an urging mechanism adapted to move the needle from a deployment configuration to a suturing configuration in which the needle is angled relative to the endoscopic device; and

wherein the needle defines at least one opening through which a suture is passed from a first side of tissue to a second side of tissue.

2. The system ofclaim 1 wherein the needle defines a lumen with the at least one opening defined near or at a distal end of the needle.

3. The system ofclaim 1 wherein the needle defines a slot along a length of the needle.

4. The system ofclaim 1 further comprising an anchor assembly removably disposed within the needle.

5. The system ofclaim 1 wherein the suture is disposed within the needle.

6. The system ofclaim 1 wherein the urging mechanism comprises a flexible delivery tube through which the needle is movable, the flexible delivery tube having a bendable section adapted to angle the needle relative to the endoscopic device.

7. The system ofclaim 1 wherein the urging mechanism further comprises an elongate pusher adapted to slide through the needle.

8. The system ofclaim 1 wherein the urging mechanism is adapted to move the needle from the deployment configuration where the needle is parallel with the endoscopic device to the suturing configuration where the needle is perpendicularly angled relative to the endoscopic device.

9. An endoscopic system for suturing tissue, comprising:

a needle adapted to travel a curved path to suture an area of tissue, the needle being removable from a distal end of an endoscopic device;

a transmission mechanism adapted to move the needle from a deployment configuration to a curved suturing configuration in which the needle is angled relative to the endoscopic device; and

wherein the needle defines at least one opening through which a suture is passed from a first side of tissue to a second side of tissue.

10. The system ofclaim 9 wherein the needle defines a lumen with the at least one opening defined near or at a distal end of the needle.

11. The system ofclaim 9 wherein the needle defines a slot along a length of the needle.

12. The system ofclaim 9 further comprising an anchor assembly removably disposed within the needle.

13. The system ofclaim 9 wherein the suture is disposed within the needle.

14. The system ofclaim 9 wherein the urging mechanism comprises a flexible delivery tube through which the needle is movable, the flexible delivery tube having a bendable section adapted to angle the needle relative to the endoscopic device.

15. The system ofclaim 9 wherein the urging mechanism further comprises an elongate pusher adapted to slide through the needle.

16. The system ofclaim 9 wherein the urging mechanism is adapted to move the needle from the deployment configuration where the needle is parallel with the endoscopic device to the suturing configuration where the needle is perpendicularly angled relative to the endoscopic device.

17. A method of suturing tissue within a hollow body organ, comprising:

positioning an endoscopic device relative to a tissue region within the hollow body organ;

piercing the tissue whereby a needle assembly travels a curved path through a flexible tubular member, the needle assembly being removable from a distal end of the endoscopic device; and

passing a length of suture through the tissue via a needle body at a distal end of the needle assembly, the needle body defining at least one opening through which the suture is passed through the tissue.

18. The method ofclaim 17 wherein positioning an endoscopic device comprises passing the endoscopic device through an esophagus and into a stomach of a patient.

19. The method ofclaim 17 wherein positioning an endoscopic device comprises positioning the distal end of the endoscopic device adjacent to the tissue region.

20. The method ofclaim 17 further comprising moving the needle assembly from a deployment configuration to a curved suturing configuration in which the needle assembly is angled relative to the endoscopic device prior to piercing the tissue.

21. The method ofclaim 17 further comprising grasping the tissue via a grasper extending from the distal end of the endoscopic device prior to piercing the tissue.

22. The method ofclaim 17 wherein piercing the tissue comprises passing the needle assembly into or through the tissue.

23. The method ofclaim 17 wherein passing a length of suture comprises delivering the suture within the needle assembly for deployment through the at least one opening.

24. The method ofclaim 17 further comprising deploying the length of suture from the at least one opening.

25. The method ofclaim 17, further comprising securing the tissue via the length of suture deployed from the needle assembly.

26. An endoscopic treatment apparatus, comprising:

an endoscopic device having a proximal end, a distal end, and a flexible length therebetween;

a needle assembly which is adapted to travel a curved path to suture an area of tissue, the needle assembly being actuatable from the proximal end of the endoscopic device to direct the needle assembly to the curved path; and

a tissue stabilizing member projecting pivotally and translationally from the distal end of the endoscopic device, the stabilizing member being adapted to hold onto the tissue when the tissue is pierced by the needle assembly.

27. The apparatus ofclaim 26 further comprising a tissue anchoring assembly deployable from the needle assembly.

28. The apparatus ofclaim 27 wherein the tissue anchoring assembly is adapted to be disposed within the needle assembly.

29. The apparatus ofclaim 26 wherein the needle assembly comprises a needle body which defines at least one opening therein.

30. The apparatus ofclaim 29 wherein the needle body defines a slot along a length thereof.

31. The apparatus ofclaim 26 further comprising a length of suture disposed within the needle assembly.

32. The apparatus ofclaim 26 further comprising an urging mechanism adapted to move the needle assembly from a deployment configuration to a suturing configuration in which the needle is angled relative to the endoscopic device.

33. The apparatus ofclaim 32 wherein the urging mechanism comprises a flexible delivery tube through which the needle assembly is movable, the flexible delivery tube having a bendable section adapted to angle the needle assembly relative to the endoscopic device.

34. The apparatus ofclaim 26 further comprising a transmission mechanism adapted to move the needle assembly from a deployment configuration to a curved suturing configuration in which the needle assembly is angled relative to the endoscopic device.

35. The apparatus ofclaim 26 wherein the tissue stabilizing member comprises a tissue grasper.

36. The apparatus ofclaim 26 wherein the tissue stabilizing member is adapted to pivotally angle relative to the endoscopic device.

37. The apparatus ofclaim 26 wherein the tissue stabilizing member is adapted to pivot when translated proximally relative to the endoscopic device.

38. A system for endoscopic treatment of tissue, comprising:

an endoscopic device having a proximal end, a distal end, and a flexible length therebetween;

a needle assembly which is adapted to suture an area of tissue, the needle assembly being actuatable from the proximal end of the endoscopic device to direct the needle assembly over a curved path;

a tissue stabilizing member projecting pivotally and translationally from the distal end of the endoscopic device, the stabilizing member being adapted to stabilize the tissue when the tissue is pierced by the needle assembly; and

a tissue anchoring assembly adapted to be deployed from the needle assembly for securing the tissue.

39. The system ofclaim 38 wherein the needle assembly comprises a needle body which defines at least one opening therein.

40. The system ofclaim 39 wherein the needle body defines a slot along a length thereof.

41. The system ofclaim 38 wherein the tissue stabilizing member comprises a tissue grasper.

42. The system ofclaim 38 wherein the tissue stabilizing member is adapted to pivotally angle relative to the endoscopic device.

43. The system ofclaim 38 wherein the tissue stabilizing member is adapted to pivot when translated proximally relative to the endoscopic device.

44. The system ofclaim 38 further comprising an urging mechanism adapted to move the needle assembly from a deployment configuration to a suturing configuration in which the needle assembly is angled relative to the endoscopic device.

45. The system ofclaim 44 wherein the urging mechanism comprises a flexible delivery tube through which the needle assembly is movable, the flexible delivery tube having a bendable section adapted to angle the needle assembly relative to the endoscopic device.

46. The system ofclaim 38 further comprising a transmission mechanism adapted to move the needle assembly from a deployment configuration to a curved suturing configuration in which the needle assembly is angled relative to the endoscopic device.

47. The system ofclaim 38 wherein the tissue anchor assembly comprises a length of suture disposed within the needle assembly.

48. A method of endoscopically treating tissue within a hollow body organ, comprising:

positioning a distal end of an endoscopic device relative to a region of tissue within the hollow body organ;

stabilizing the tissue via a stabilizing member projecting pivotally and translationally from the distal end of the endoscopic device;

piercing the tissue with a needle assembly which is adapted to suture the tissue by actuating the needle assembly from a proximal end of the endoscopic device such that the needle assembly is directed over a curved path; and

passing a length of suture through the tissue via the needle assembly.

49. The method ofclaim 48 wherein positioning a distal end of an endoscopic device comprises advancing the endoscopic device through an esophagus and into a stomach of a patient.

50. The method ofclaim 48 wherein stabilizing the tissue via a stabilizing member comprises articulating the stabilizing member proximally while grasping the tissue.

51. The method ofclaim 48 wherein stabilizing the tissue via a stabilizing member comprises pulling the tissue proximally and pivoting the stabilizing member relative to the tissue.

52. The method ofclaim 48 wherein piercing the tissue comprises passing a needle body positioned at a distal end of the needle assembly into or through the tissue.

53. The method ofclaim 48 further comprising flexing a portion of a tubular member through which the needle assembly is translatable to form the curved path prior to piercing the tissue.

54. The method ofclaim 48 wherein passing a length of suture comprises deploying the suture from the needle assembly after piercing the tissue.

55. The method ofclaim 48 further comprising deploying a tissue anchor assembly from the needle assembly.

56. The method ofclaim 55 further comprising securing the tissue via the tissue anchor assembly.

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