US20200046349A1 - Method for suture lacing - Google Patents

Abstract

A method for suture lacing includes providing a suture with a needle attached thereto, inserting the needle and suture into an organ through a passageway, throwing a single stitch through a first tissue member, throwing a single stitch through an opposed and spaced apart second tissue member, repeating the preceding step at least once, bringing the first and second tissue members in contact by tensioning the suture, whereby suture drag is minimized during the tensioning and even tissue compression substantially achieved, and securing the suture.

Description

CROSS REFERENCE TO RELATED APPLICATION
• This application is a continuation-in-part of U.S. patent application Ser. No. 11/150,481, entitled “ENDOSCOPIC SUTURING DEVICE”, filed Jun. 13, 2005, which is currently pending.
BACKGROUND OF THEINVENTION1. Field of the Invention
• The invention relates to a method for suturing lacing.
2. Description of the Prior Art
• Endoscopic procedures have been rapidly developing over the past decade. These procedures often allow for the performance of surgical procedures with minimal trauma when compared to prior techniques requiring a large external opening to expose the internal organ or tissue requiring repair.
• In addition to the many areas in which endoscopic procedures have found use, endoscopic procedures have been developed for surgical procedures addressing morbid obesity. Morbid obesity is a serious medical condition. In fact, morbid obesity has become highly pervasive in the United States, as well as other countries, and the trend appears to be heading in a negative direction. Complications associated with morbid obesity include hypertension, diabetes, coronary artery disease, stroke, congestive heart failure, multiple orthopedic problems and pulmonary insufficiency with markedly decreased life expectancy. With this in mind, and as those skilled in the art will certainly appreciate, the monetary and physical costs associated with morbid obesity are substantial. In fact, it is estimated the costs relating to obesity are in excess of 100 billion dollars in the United States alone.
• A variety of surgical procedures have been developed to treat obesity. One procedure is Roux-en-Y gastric bypass (RYGB). This operation is highly complex and is commonly utilized to treat people exhibiting morbid obesity. Around 35,000 procedures are performed annually in the United States alone. Other forms of bariatric surgery include Fobi pouch, bilio-pancreatic diversion, and gastroplasty or “stomach stapling”. In addition, implantable devices are known which limit the passage of food through the stomach and affect satiety.
• RYGB involves movement of the jejunum to a high position using a Roux-en-Y loop. The stomach is completely divided into two unequal portions (a smaller upper portion and a larger lower gastric pouch) using an automatic stapling device. The upper pouch typically measures less than about 1 ounce (or 20 cc), while the larger lower pouch remains generally intact and continues to secret stomach juices flowing through the intestinal track.
• A segment of the small intestine is then brought from the lower abdomen and joined with the upper pouch to form an anastomosis created through a half-inch opening, also called the stoma. This segment of the small intestine is called the “Roux loop” Roux limb and carries the food from the upper pouch to the remainder of the intestines, where the food is digested. The remaining lower pouch and the attached segment of duodenum are then reconnected to form another anastomotic connection to the Roux loop limb at a location approximately 50 to 150 cm from the stoma, typically using a stapling instrument. It is at this connection that the digestive juices from the bypass stomach, pancreas, and liver, enter the jejunum and ileum to aide in the digestion of food. Due to the small size of the upper pouch, patients are forced to eat at a slower rate and are satiated much more quickly. This results in a reduction in caloric intake.
• As those skilled in the art will certainly appreciate, the conventional RYGB procedure requires a great deal of operative time. Because of the degree of invasiveness, post-operative recovery time can be quite lengthy and painful. In view of the highly invasive nature relating to the current RYGB procedure, other less invasive procedures have been developed. With this mind other procedures for reducing the size of the stomach have been developed. The most common form of gastric reduction surgery involves the application of vertical staples along the stomach to create an appropriate pouch. This procedure is commonly performed laparoscopically and as such requires substantial preoperative, operative, postoperative resources.
• As endoscopic devices and procedures have developed, surgeons have begun to employ endoscopic techniques to gastric procedures such as those discussed above in an effort to minimize trauma and reduce the time required for procedures and recovery. With the foregoing in mind, procedures and apparatuses that allow for the performance of gastric reduction surgery in a time efficient and patient friendly manner are needed.
• One area that has not been adequately addressed is the need for the application of sutures as these gastric, and other endoscopic, procedures are being performed.
• The present invention provides an endoscopic suturing device adapted for the continuous application of sutures.
SUMMARY OF THE INVENTION
• It is, therefore, an object of the present invention to provide a method for suture lacing including providing a suture with a needle attached thereto, inserting the needle and suture into an organ through a passageway, throwing a single stitch through a first tissue member, throwing a single stitch through an opposed and spaced apart second tissue member, repeating the preceding step at least once, bringing the first and second tissue members in contact by tensioning the suture, whereby suture drag is minimized during the tensioning and even tissue compression substantially achieved, and securing the suture.
• It is also an object of the present invention to provide a method wherein the suture includes first and second leads, and the step of securing includes knotting the first and second leads of the suture.
• It is another object of the present invention to provide a method wherein the suture includes first and second leads and the step of securing includes anchoring at least one of the first and second leads of the suture to tissue.
• It is a further object of the present invention to provide a method wherein the step of securing includes anchoring both the first and second leads of the suture to tissue.
• It is also another object of the present invention to provide a method wherein the step of inserting includes insertion through a natural orifice of a patient.
• It is also a further object of the present invention to provide a method wherein the step of inserting includes insertion through an orifice from approximately 3 mm to approximately 24 mm in diameter.
• It is still another object of the present invention to provide a method wherein the step of inserting includes insertion through a trocar.
• It is yet a further object of the present invention to provide a method wherein the step of inserting includes insertion through an orifice from approximately 3 mm to approximately 18 mm in diameter.
• It is also an object of the present invention to provide a method including a step of reversing the direction of a final suture throw.
• It is another object of the present invention to provide a method wherein the step of reversing includes positioning a reversing pin between the suture and either the first tissue member or the second tissue member.
• Other objects and advantages of the present invention will become apparent from the following detailed description when viewed in conjunction with the accompanying drawings, which set forth certain embodiments of the invention.
BRIEF DESCRIPTION OF THE DRAWINGS
• FIG. 1 is a perspective view of the present invention with the vacuum chamber secured thereto.
• FIG. 2 is a perspective view of the present invention without the vacuum chamber.
• FIGS. 3 through 10 are cut away views demonstrating operation of the present invention.
• FIG. 11 is a perspective view showing a suturing body with a vacuum chamber in accordance with a preferred embodiment secured thereto.
• FIG. 12 shows an alternate vacuum chamber secured to the suturing body.
• FIGS. 13 and 14 are top views of yet another vacuum chamber secured to the suturing body, whereinFIG. 13 shows the vacuum chamber in its expanded configuration andFIG. 14 shows the vacuum chamber in its low profile configuration.
• FIG. 15 is a cut away view of the suturing body showing a smooth friction camming member.
• FIG. 16 is an alternate embodiment of the suturing body showing a toothed friction camming member.
• FIG. 17 is a cut away view of yet another embodiment of the suturing body with a gear driven friction camming member.
• FIGS. 18 and 19 are cut away views of the suturing body showing alternate back-up mechanisms which may be utilized in accordance with the present invention.
• FIGS. 20, 21 and 22 are various views of a suturing body including a cam pin set mechanism utilized in selectively opening the suture housing.
• FIGS. 23 and 24 are bottom views of a suturing body showing a tear strip mechanism utilized in selectively opening the suture housing.
• FIGS. 25 and 26 are bottom views of a suturing body showing yet another mechanism utilized in selectively opening the suture housing.
• FIGS. 27 and 28 are bottom views of a suturing body showing a spreader plate mechanism utilized in selectively opening the suture housing.
• FIGS. 29, 30 and 31 are various views of a suturing body showing an alternate mechanism for selectively opening the suture housing.
• FIG. 32 is a cut away view of the suturing body showing a needle position indicating mechanism.
• FIG. 33 is a cut away view of the suturing body showing an alternate needle position indicating mechanism.
• FIG. 34 is perspective view of a suturing body employing an alternate needle position indicating mechanism wherein an indicator pin is shown in its hidden position.
• FIG. 35 is a cross sectional view of the needle position indicating mechanism shown inFIG. 34 with the indicator pin shown in its hidden position.
• FIG. 36 is perspective view of the suturing body shown inFIG. 34 with the indicator pin in its exposed position.
• FIG. 37 is a cross sectional view of the needle position indicating mechanism shown inFIG. 36 with the indicator pin in its exposed position.
• FIG. 38 is a detailed side, cut away view showing a colored needle utilized in needle position identification.
• FIG. 39 is a perspective view showing a visual indicator linked to various sensors for identifying needle position.
• FIGS. 40, 41, 41a,42,42aand43 are various views showing an attachment mechanism for securing the present suturing apparatus to an endoscope.
• FIGS. 44, 45 and 46 show a guidewire introducer mechanism for use in conjunction with the present suturing apparatus.
• FIGS. 47, 48, 49, 50 and 51 disclose a detachable handle mechanism for utilization in conjunction with the present suturing apparatus.
• FIGS. 52 through 61 disclose various techniques for suture lacing in accordance with the present invention.
• FIG. 62 is a perspective view of a knotting element in accordance with the present invention.
• FIG. 63 is a perspective view showing fusing of knotted sutures.
• FIGS. 64, 65, 66, 67 and 68 are perspective views showing various suction vacuum assist mechanisms in accordance with the present invention.
• FIG. 69 shows a suturing technique utilizing an adhesive/sealant.
• FIGS. 70, 71 and 72 show a perforated suture utilized in supplying adhesive/sealant to a suture line.
• FIGS. 73 through 81 disclose a procedure whereby a stomach pouch is created through the application of an adhesive/sealant.
• FIGS. 83 and 84 are perspective views of a suturing apparatus incorporating an imaging device within the suturing body.
• FIG. 85 is a cut away view of the suturing body showing a cartridge mechanism for utilization therewith.
• FIG. 86 is a cut away view of the suturing body showing a cartridge mechanism having a smaller needle.
• FIGS. 87 and 88 are side views showing a needle loading mechanism in accordance with the present invention.
• FIGS. 89, 90 and 91 disclose screw-based mechanisms for adjusting the size of the vacuum chamber and central opening.
• FIG. 92 is a cut away view showing a wire-based mechanism for adjusting the effective depth of the vacuum chamber and central opening.
• FIG. 93 is a top view showing a cinching line utilized in adjusting the effective size of the vacuum chamber and central opening.
DESCRIPTION OF THE PREFERRED EMBODIMENTS
• The detailed embodiments of the present invention are disclosed herein. It should be understood, however, that the disclosed embodiments are merely exemplary of the invention, which may be embodied in various forms. Therefore, the details disclosed herein are not to be interpreted as limiting, but merely as the basis for the claims and as a basis for teaching one skilled in the art how to make and/or use the invention.
• With reference toFIGS. 1 to 10, anendoscopic suturing apparatus10 for the continuous application of asuture12 is disclosed. The term “suture” as used throughout the body of the present application is intended to refer to a variety of flexible securing filaments whether they be made of natural filament, synthetic or polymeric filaments, or metallic wire filaments.
• Although the present suturing apparatus is particularly adapted for use in performing endoscopic gastric reduction procedures, those skilled in the art will certainly appreciate the apparatus may be used for a wide variety of applications without departing from the spirit of the present invention. More particularly, the present suturing apparatus is shaped and dimensioned for insertion through a natural orifice of a patient, for example, transorally, and is, therefore, shaped and dimensioned for insertion through an orifice from approximately 3 mm to approximately 24 mm in diameter. Although the present suturing apparatus is particularly adapted for insertion through a patient's natural orifice, the present suturing apparatus may be shaped and dimensioned for laparoscopic insertion through a trocar, and is, therefore, shaped and dimensioned for insertion through an orifice from approximately 3 mm to approximately 18 mm in diameter.
• Thesuturing apparatus10 includes asuturing body14 shaped and dimensioned for attachment to thedistal end16 of a commercially available endoscope, or other supporting structure,18 in a manner permitting actuation thereof and the creation of a vacuum. With this in mind, the suturingbody14 is secured to theendoscope18 using known attachment structures appreciated by those skilled in the art.
• The suturingbody14 is composed of afirst housing member20 and asecond housing member22 secured together to create asuture housing24 in which the functional components of thepresent apparatus10 are housed for movement in accordance with the present invention. Thesuture housing24 includes an innerfirst track26 in which aneedle28 is positioned for movement about a predetermined continuous circular path under the control of adrive assembly30.
• Although the present suturing apparatus is disclosed in accordance with a preferred embodiment as providing for the translation of the needle about a continuous circular path, it is contemplated many of the concepts underlying the present invention may be applied in systems wherein the needle is merely moved along an arcuate path, and not necessarily along a continuous circular path.
• Thedrive assembly30 is supported within second andthird tracks32,34 positioned about the innerfirst track26. Thedrive assembly30 applies axial motion to cause movement of theneedle28 about its continuous circular path. Thedrive assembly30 is generally composed of afriction plate36 statically mounted along thesecond track32 and afriction camming member38 that moves along thesecond track32 while apin40 moves along the outerthird track34. Adrive cable42 is coupled to thepin40 for controlling actuation thereof in the manner described below in greater detail. Thedrive cable42 is actuated for movement of thedrive assembly30 by a handle (for example, as shown inFIGS. 47 to 51). Although a preferred handle is disclosed below, it is contemplated a variety of handle structures may be utilized in the actuation of the drive cable without departing from the spirit of the present invention.
• For reasons that will become apparent based upon the operation of thepresent suture apparatus10 as described below in greater detail, the suturingbody14 is substantially C-shaped with acentral opening44 in which tissue is positioned during suturing. The C-shape of thesuturing body14 allows theneedle28 to move about a circular path during operation thereof and pass through tissue positioned with the central opening.
• Referring toFIGS. 1 and 2, and in accordance with a preferred embodiment, the presentendoscopic suturing apparatus10 is attached to a commerciallyavailable endoscope18 by way of aclamp17. As briefly mentioned above, and as discussed below in greater detail, thesuturing apparatus10 may be secured to theendoscope18 in a variety of ways without departing from the spirit of the present invention. Thesuturing apparatus10 is oriented in a way that allows the user to maintain visibility of theneedle28 and operative field, as well as create a small cross section to aid in transoral insertion (when thesuturing apparatus10 is used in gastric surgical procedures).
• Avacuum chamber46 surrounds and/or otherwise contains thesuturing body14 of thepresent suture apparatus10. This defines acavity48 in which thesuturing body14 sits. Thevacuum chamber46 is coupled to thevacuum line50, which is coupled in tandem to theendoscope18, but not in the working channel of theendoscope18, such that a vacuum is created within thecavity48 defined by thevacuum chamber46, as well as thecentral opening44 of thesuturing body14. In this way, the application of the vacuum draws adjacent tissue into thecentral opening44 of thesuturing body14.
• As briefly mentioned above, thepresent suturing apparatus10 is provided with avacuum chamber46 designed to enhance one's ability to draw tissue into a position for suturing. Thevacuum chamber46 is shaped and dimensioned to facilitate pulling the tissue wall into thevacuum chamber46, and particularly, thecentral opening44 of thesuturing body14, under the control of the applied vacuum. Once drawn within thevacuum chamber46 and thecentral opening44, the tissue is held therein as theneedle28 is passed therethrough while thesuturing body14 throws stitches. The requiredvacuum chamber46 size is based upon the thickness of the tissue being sutured. The vacuum necessary to pull the desired tissue thickness is proportionate to both the thickness of the tissue and the size of thevacuum chamber46.
• As a result, thepresent vacuum chamber46 attempts to increase the size thereof to minimize the required vacuum for accomplishing the task, without making thevacuum chamber46 too large for passage into the stomach. The ability of thepresent vacuum chamber46 to achieve desired suction with vacuum pressure provided at a hospital or other medical facility is especially important considering the magnitude of vacuum sources available at different hospitals, as well as within different surgical suites, varies greatly.
• With this in mind, and in accordance with preferred embodiments of the present invention as shown inFIGS. 11 and 12, (where similar reference numerals are used for similar parts) thevacuum chamber146 is constructed from a resilient elastomer. It is cup-like in its configuration and generally includes aninner wall170 and anouter wall172. Theinner wall170 of thevacuum chamber146 is preferably provided with projections, for example, ribs and/or hooks,174 (as shown inFIG. 12) to further improve the ability of thevacuum chamber146 to retain tissue drawn thereon under suction. Theseprojections174 provide grabbing surfaces for the tissue to be pinned against when the vacuum is applied to thevacuum chamber146. Theprojections174 also increase the holding power of the vacuum thereby minimizing the amount of vacuum needed.
• In accordance with a preferred embodiment, thevacuum chamber146 is composed of first and secondvacuum chamber members176,178 secured to opposite sides of thesuturing body114 in a manner containing, or otherwise surrounding, the functional components of thesuturing body114. The first andsecond chamber members176,178 are mirror images of each other and define a space surrounding thesuturing body114 for the creation of a vacuum. In accordance with a preferred embodiment, the first and secondvacuum chamber members176,178 define a cup-like space in which thesuturing body114 is positioned.
• Each of the first and secondvacuum chamber members176,178 includes a semicircularupper edge184 and a concavelower portion186. As such, when the first and secondvacuum chamber members176,178 are secured along opposite sides of thesuturing body114, the cup-like space is defined about thesuturing body114. The cup-like space provides a confined space in which the suction provided by the vacuum is constrained so as to securely and efficiently draw tissue into thecentral opening144 of thesuturing body114.
• The first and secondvacuum chamber members176,178 of thevacuum chamber146 are manufactured from an elastomer, for example, urethane, adiprene or santoprene. Thevacuum chamber146 is designed to permit expansion and contraction thereof. The provision of anexpandable vacuum chamber146 maximizes chamber size to increase tissue inclusion during vacuum application, while permitting reducedvacuum chamber146 size during insertion of thesuturing apparatus110. More particularly, the ability of thevacuum chamber146 to expand and contract facilitates trans-oral passage of thesuturing apparatus110 while similarly optimizingvacuum chamber146 size during tissue suction.
• As those skilled in the art will appreciate, the need for trans-oral passage of thesuturing apparatus110 defines an ultimate limit on the dimensions of thesuturing apparatus110 and, therefore, thevacuum chamber146 that can be introduced to capture tissue in accordance with the present invention. The larger thevacuum chamber146, the larger the “bite” of tissue that can be captured in one throw of thesuturing apparatus110. With this in mind, and as discussed above, thevacuum chamber146 is made out of an elastomer allowing it to be collapsed during insertion and then “spring” back to its original shape after it is fully inserted.
• In accordance with an alternate embodiment, and with reference toFIGS. 13 and 14, expansion of thevacuum chamber246 is further facilitated by the provision of living hinges280 at predefined bending points of thecavity248 defined by thevacuum chamber246. This allows thevacuum chamber246 to be constructed of a wider variety of materials, including non-elastic plastics, since the living hinges280 permit the more rigid structures to “fold” rather than elastically bend. More particular, and with reference to the prior embodiment, thevacuum chamber246 is composed of a firstvacuum chamber member276 and a secondvacuum chamber member278. The first and secondvacuum chamber members276,278 are mirror images of each other, and each includes a semi-circularupper section284 and a concavelower section286. As a result, the first and secondvacuum chamber members276,278 are coupled to opposite sides of thesuturing body214 to form thepresent vacuum chamber246, which can similarly include the ribs and/or hooks discussed above with regard to the prior embodiment.
• In accordance with a preferred embodiment, the first and secondvacuum chamber members276,278 are constructed of a semi-rigid material and, therefore, respectively include living hinges280 permitting expansion and contraction thereof. The living hinges280 are positioned at predefined bending points of the first and secondvacuum chamber members276,278 in a manner optimizing folding thereof. The living hinges280 permits controlled expansion and contraction of thevacuum chamber246 as the first and secondvacuum chamber members276,278 are moved relative to each other in accordance with the present invention. One is, therefore, able to pass avacuum chamber246 that is ultimately, when used, larger than the trans-oral space through which it is passed.
• Those skilled in the art will appreciate it is would be desirable to make a vacuum chamber and central opening adapted to accommodate any type of tissue, any thickness of tissue and be able to allow the user to adjust the bite size (that is, the extent of tissue through which the suture is thrown). To this end, various embodiments for the adjustment of the effective vacuum chamber and central opening size have been developed and are disclosed herein. These embodiments also allow for longitudinal and lateral adjustment of the vacuum chamber, as well as depth adjustment of the central opening and vacuum chamber, to allow for use with different tissue thicknesses, different tissue types and variable tissue bites per suture throw. In this way the surgeon is allowed to readily adjust the effective vacuum chamber/central opening depth, width and/or length to allow for adjustment of the depth of the tissue bite, which controls the depth of the needle path through the tissue (i.e., full thickness or partial thickness). The ability for adjustment also allows the same suturing apparatus to be used for multiple tissue types and thicknesses. While limiting the maximum amount of tissue that may be drawn into the vacuum chamber and central opening, the present techniques may also be applied to ensure that a predetermined and controlled amount of tissue is drawn into the vacuum chamber and the central opening.
• In accordance with a preferred embodiment, and with reference toFIGS. 89, 90 and 91, adjustment is accomplished by the provision of adjustingscrews3970 in thebase3972 of thevacuum chamber3946. Thescrews3970 respectively allow for longitudinal or lateral adjustment of thevacuum chamber3946 by adjusting ascrew3970 in thebase3972 of thevacuum chamber3946 that expands or contracts thevacuum chamber3946 in a desired direction.
• In accordance with another embodiment, and with reference toFIG. 88 awire4070 is used to raise the effective base of thevacuum chamber4046 and thecentral opening4044 controlling the effective depth of thevacuum chamber4046 and thecentral opening4044. Thiswire4070 is a buckled spacing wire that can be further buckled or allowed to straighten, effectively reducing the depth to which the tissue can enter the cavity defined by thecentral opening4044 and thevacuum chamber4046. The straighter thespring wire4070 is allowed to be, the higher the effective bottom of the cavity is set. Thespring wire4070 thereby prevents deep entrance of tissue (that is, entrance beyond the barrier created by the spring wire4070) into thecentral opening4044. The slack in thewire4070 is controlled via ascrew member4072 found within the suturing body4014 for actuation of thewire4070.
• Referring toFIG. 93, and in accordance with another embodiment, a cinchingcable4170 is used to adjust the effective length of the vacuum chamber4148. In particular, a cinchingcable4170 is threaded about the outer perimeter of thevacuum chamber4146, with the free ends4172,4174 thereof exiting at the proximal end of thevacuum chamber4146. As such, the free ends4172,4174 may be tensioned to shorten thevacuum chamber4146 length, and similarly released when it is desired to increase the length of thevacuum chamber4146 by allowing the walls thereof to expand to their unbiased position.
• As mentioned above, thehousing24 contains theneedle28 used in the application of asuture12 to the tissue drawn within thecentral opening44. Thesuture12 is secured to the proximal end, that is, the blunt end, of theneedle28 and is drawn through the tissue as theneedle28 is actuated in accordance with the present invention as described herein. In accordance with a preferred embodiment, theneedle28 is curved to rotate about a predetermined continuous circular path and extends along an arc of 240 degrees creating an opening of 120 degrees. However, those skilled in the art will appreciate the opening may be varied; for example, it has been contemplated to use a needle offering an opening of 140 degrees.
• Theneedle28 includes aninterior surface52 along the inner surface of the arc defined by theneedle28 and anexterior surface54 along the outer surface of the arc defined by theneedle28. A series ofnotches56 are cut into theexterior surface54 of theneedle28. As will be appreciated based upon the following description, thenotches56 are shaped and dimensioned for use by thedrive assembly30 in grabbing, driving and releasing theneedle28. Although notches along the exterior surface of the needle are disclosed for use in accordance with a preferred embodiment of the present invention, it is contemplated the needle may be formed without notches such that the drive assembly merely grips the substantially smooth exterior surface of the needle to drive it forward.
• Operation of thedrive assembly30 and movement of theneedle28 is described with reference toFIGS. 3 to 10, wherein one half of thehousing24 is removed exposing internal components of thepresent suture apparatus10. The drive cable42 (shown inFIG. 3) is rigidly attached to thepin40. As is described below in greater detail, thedrive cable42,pin40 andfriction camming member38 are extended and retracted to engage and disengage theneedle28 for movement thereof about its circular path. Thedrive cable42 is flexible enough to curve in thehousing24 and flex along with theendoscope18, but is rigid enough to be compressed to drive thefriction camming member38 into its initial drive stage (seeFIG. 4).
• Thefriction camming member38 is composed of anarcuate engagement member58 and acamming member60 working in conjunction with thepin40 to control the position of theengagement member58 for selective engagement with theneedle28. Theengagement member58 is constructed withinternal notches62 shaped and dimensioned for engaging theneedle28 to drive it in a clockwise direction, but permit free movement thereof as thefriction camming member38, that is, both theengagement member58 and thecamming member60, is moved in a counter-clockwise direction toward the initial drive stage.
• Theengagement member58 of thefriction camming member38 is designed to translate in thehousing24 both radially towards and away from theneedle28, as well as translate arcuately clockwise and counterclockwise about the arc defined by thehousing24. This is achieved through the camming action offered by the interaction between thecamming member60, thepin40 and theengagement member58. Thecamming member60 is rigidly coupled to theengagement member58 such that theengagement member58 is moved into and out of engagement with theneedle28 as the radial position of thecamming member60 is altered based upon its interaction with thepin40. As discussed below in accordance with an alternate embodiment, it is contemplated that a spring element may be employed to force thefriction camming member38 against theneedle28.
• More particularly, as thedrive cable42 is compressed (that is, thedrive cable42 is pushed distally away from the operation of the suturing apparatus10) to move thefriction camming member38 in a counter-clockwise direction, thepin40 slides within aslot64 formed in thecamming member60 forcing theengagement member58 andcamming member60 to move counterclockwise as well as outwardly from theneedle28. Thefriction plate36 aids in forcing theengagement member58 outwardly from theneedle28 as thefriction camming member38 is moved in this counter-clockwise direction.
• With thefriction camming member38 in its initial drive position as shown inFIG. 4, and as tension is applied to the drive cable42 (that is, thedrive cable42 is pulled proximally toward the operation of the suturing apparatus10) and ultimately thepin40, thepin40 engages thecamming member60 forcingfriction camming member38, and more particularly, theengagement member58 to travel inwardly into contact with theexterior surface54 of theneedle28 due to the camming action resulting from the interaction of thepin40 and theslot64 within the camming member60 (seeFIG. 5). As tension is continually applied to thedrive cable42 thenotches62 formed along the inner surface of theengagement member58 grab into thenotches56 cut into theexterior surface54 of theneedle28, causing theneedle28 to rotate clockwise untilpin40 reaches the limit oftrack34 and the procedure must start all over (seeFIG. 6).
• When the limit of the stroke is reached as shown inFIG. 6, the operator compresses thedrive cable42 causing theengagement member58 to disengage from theneedle28 by way of the cam feature resulting from the interaction of thepin40 within theslot64 of thecamming member60 as thepin40 slides within theslot64 causing theengagement member58 andcamming member60 to move outwardly and in a counterclockwise direction (seeFIG. 7). The compression on thedrive cable42 is continued until thefriction camming member38 moves counterclockwise reaching the opposite end of the housing24 (seeFIG. 8). Tension is then applied to once again move theneedle28 in a clockwise direction and the procedure is repeated until the needle has traveled 360 degrees (seeFIGS. 9 and 10).
• As briefly discussed above, thedrive assembly30 of the present invention is capable of driving theneedle28 about its circular path in a highly controlled and efficient manner. Referring toFIG. 15, the functionality of thepresent drive assembly330 is enhanced by the provision of thefriction camming member338, which drives theneedle328 when pulling theneedle328 along its path through frictional means. The contact surface of thefrictional interface358 of thefriction camming member338 is manufactured to enhance its frictional relationship with theneedle328 so as to smoothly and reliably move theneedle328 in accordance with the present invention.
• The interaction between thefriction camming member338 and theneedle328 is enhanced by the provision of aleaf spring370. Theleaf spring370 extends within thesuture housing324 of thesuturing apparatus310 and is oriented to contact thefriction camming member338 during actuation of theneedle328 for forcing thefriction camming member338 into contact with theneedle328. Theleaf spring370 is a cantilever mounted spring member mounted proximally of thefriction camming member338. As thefriction camming member338 is forced distally, theleaf spring370 increases the engagement forces radially the farther thefriction camming member338 is displaced. As those skilled in the art will certainly appreciate, a spring structure is disclosed in accordance with a preferred embodiment of the present invention and other spring structures could be employed without departing from the spirit of the present invention.
• In accordance with an alternate embodiment, and with reference toFIG. 16, the smoothfriction camming member338 discussed above may be replaced with a toothedfriction camming member438. In accordance with this embodiment, the contact surface of thefrictional interface458 of thefriction camming member438 is provided withteeth472 shaped and dimensioned to engage similarly shapedteeth474 formed along the exterior surface ofneedle428. In this way, theteeth472 along thefrictional interface458 of thefriction camming member438 engageteeth474 cut into theneedle428 and drag theneedle428 along its drive path when pulled. As with the prior embodiment, the interaction between thefriction camming member438 and theneedle428 is enhanced by the provision of aleaf spring470. Theleaf spring470 extends within thesuture housing424 of thesuturing apparatus410 and is oriented to contact thefriction camming member438 during actuation of theneedle428 for forcing thefriction camming member438 into contact with theneedle428.
• In accordance with an alternate embodiment, and with reference toFIG. 17, The motion of the friction camming member538 (whether it be a smoothfriction camming member338 as shown inFIG. 15 or a toothedfriction camming member438 as shown inFIG. 16) used in driving theneedle528 can also be achieved through the use of asprocket gear570 engaging withteeth572 on theback side574 of thefriction camming member538 driving theneedle528 through the same motions the linear pull system created. Such a gearing arrangement provides for the translation of rotary motion along thedrive cable582, and about a first axis substantially aligned with the longitudinal axis of thesuturing apparatus510 extending through thesuturing apparatus510, into rotary motion of theneedle528 about an arcuate path having a central axis substantially perpendicular to the longitudinal axis of thesuturing apparatus510. In accordance with this embodiment, thesprocket gear570 is rotated by a rotarycable drive system576 linked to a rotary member in the handle (not shown) which would replace the linear pull system. In accordance with this embodiment, the rotary cable motion (rotating about the longitudinal axis of the device shaft) is converted to rotary motion (rotating perpendicular to the longitudinal axis of the device shaft) to drive theneedle528 directly along its circular path or to drive the toothedfriction camming member538 in its path.
• More particularly, thedrive cable582 is designed for rotation about an axis substantially parallel to the longitudinal axis of theapparatus510. Thedistal end584 of thedrive cable582 is provide withspur gear586 which is linked to asimilar spur gear588 mounted between thespur gear586 at thedistal end584 of thedrive cable582 and a gearedcontact surface574 of thefriction camming member538. As a result, rotation of thedrive cable582 causes thespur gear586 to rotate, which in turns translates into motion of thefriction camming member538. Movement of thefriction camming member538 then causes theneedle528 to move in a desired arcuate path. Since thefriction camming member538 engages and disengages theneedle528 in a manner similar to the embodiment described above, movement of theneedle528 is achieved by alternately reversing the rotation of the rotary cable system. Forward rotation cams thefriction camming member538 into engagement and drives thefriction camming member538 counter-clockwise in a manner driving theneedle528. Reverse rotation of thedrive cable582 disengages thefriction camming member538 from theneedle528 and rotates thefriction camming member538 clockwise resetting it for the next driving motion.
• Regardless of the friction camming member design, the drive mechanism employed in accordance with preferred embodiments of the present invention provides a rotary needle drive system for suture pass-through capable of multiple tissue pass-through during a single device insertion. As discussed above, in accordance with a preferred embodiment of the present invention, this is accomplished by a friction camming member that advances the needle by means of a toothed engagement or a frictional coupling, and provides for needle advancement permitting variation in the size of both the needle and suture used in accordance with the present invention.
• Two anti-backup structures are disclosed with reference toFIGS. 18 and 19. These anti-backup structures control needle movement so the needle is only allowed to pass in one direction. This prevents the needle from backing out between actuating strokes of the friction camming member as it moves between its end (or limit) of stroke position as shown inFIG. 6 and its initial drive position as shown inFIG. 8. More particularly, the needle of the present suturing apparatus is designed to move in a predetermined first direction about an arcuate path, and movement in an opposite second direction is undesired. As such, the present anti-backup structures prevent movement of the needle in the second direction while permitting free movement of the needle in the first direction.
• More particularly, and in accordance with a preferred embodiment disclosed with reference toFIG. 18, a frictionalanti-backup device670 is secured along the forward end of theneedle628 path for contact with theneedle628 in a manner preventing undesired back-up thereof. The frictionalanti-backup device670 is alever arm672 including afirst end674 andsecond end676. Thefirst end674 of thelever arm672 is pivotally secured to thesuturing body614 of thesuturing apparatus610. Thesecond end676 oflever arm672 extends toward, and into contact with, the contact surface of theneedle628. Thelever arm672 is oriented such that when theneedle628 is moved in a counter-clockwise direction as viewed inFIG. 18, thelever arm672 slides over the exterior surface of theneedle628 permitting theneedle628 to freely rotate.
• However, if theneedle628 attempts to rotate in a clockwise direction as viewed inFIG. 18, thesecond end676 of thelever arm672 frictionally engages the exterior surface of theneedle628 in a manner stopping clockwise rotation thereof. This is a result of the orientation of thelever arm672 that creates a frictional impediment to movement of theneedle628, for example, similar to a ratchet mechanism. With this in mind, thelever arm672 is biased to maintain engagement with the exterior surface of theneedle628 whether the needle is rotated in a clockwise direction or a counter-clockwise direction.
• In accordance with an alternate embodiment and with reference toFIG. 19, thesuturing body714 is provided with an integral springbiased latch770 shaped and dimensioned to fit withinrecesses772 formed in the exterior surface of theneedle728. With this in mind, thelatch770 and therecesses772 are shaped and dimensioned to permit substantially free rotation of theneedle728 in one direction while preventing rotation of theneedle728 in the opposite direction.
• Since it is possible the needle may become jammed within the tissue during deployment, it sometimes becomes necessary to free the needle from the suturing apparatus for emergency extraction of both the suturing apparatus and the needle. With this in mind, and with reference to the various embodiments presented below, techniques have been developed for freeing the needle in the event it becomes jammed and requires release. In general, the embodiments described below are different methods of separating or opening the suture housing of the suturing apparatus to release the needle and allow the suturing apparatus to be removed. Release of the needle in this manner might necessitate subsequent removal of the needle from its jammed position, but will permit extraction of the remainder of the suturing apparatus as the suturing apparatus is no longer hung on the tissue based upon the release of the needle.
• In accordance with the various embodiments disclosed below, a surgical suturing apparatus includes a suture housing and a needle mounted within the suture housing for movement about an arcuate path. The suturing apparatus also includes a drive assembly operably associated with the needle for controlling movement of the needle with a suture secured thereto about the arcuate path in a manner facilitating application of the suture to tissue. The suture housing has an open position and a closed position, and the needle can be removed from the suture housing when in the open position.
• The various embodiments provide a user a controlled opening mechanism that allows the suture housing to be selectively opened should the needle fail to be able to advance and the suturing apparatus needs to be extracted. As will be described below in greater detail, this is achieved by employing either a spring biased, hinged clamshell suturing body opening when a crushable coupling mechanism is actuated, a removable pin/cable mechanism that holds the two halves of the suturing body together or an openable suture deployment system that can be re-closed for extraction from the body.
• In accordance with a first embodiment, and with reference toFIGS. 20 to 22, and as discussed above in greater detail, thesuturing body814 is composed of afirst housing member820 andsecond housing member822 making up thesuture housing824. A cam pin set870 locks thefirst housing member820 and thesecond housing member822 together, with, however, the ability to remove the cam pin set870 from thesecond housing member822 when it is desired to separate the first andsecond housing members820,822 for removal of ajammed needle828.
• More particularly, the first andsecond housing members820,822 are hinged872 along one end thereof, and the cam pin set870 is positioned in a manner opposite thehinge872 so the first andsecond housing members820,822 are securely held together. However, when the cam pin set870 is removed, or otherwise removed from its locking position with asecond housing member822, the first andsecond housing members820,822 are free to move apart pivoting about thehinge872. Opening of the suturinghousing824 is further facilitated by the inclusion of aspring874 in thehinge872 for encouraging opening of the suturinghousing824 upon removal of the cam pin set870.
• Actuation of the cam pin set870 is achieved via the use of arelease member876 that interacts to permit controlled locking and release of the cam pin set870. In particular, therelease member876 includes a series ofinterference members878 which interact with theheads880 of the cam pin set870 to retain them withinrecesses882 formed in the second housing member822 (seeFIG. 21). When it is desired to separate the first andsecond housing members820,822, therelease member876 is shifted, for example, via a cable884 extending for actuation by a user, to move theinterference member878 and allow the cam pin set870 to move from within the second housing member822 (seeFIG. 22).
• In accordance with another embodiment, and with reference toFIGS. 23 and 24, atear strip970 is disclosed. As with the prior embodiments, thesuturing body914 is composed of afirst housing member920 andsecond housing member922 making up thesuture housing924. The first andsecond housing members920,922 are hinged972 along one end thereof, with aspring974 biasing the first andsecond housing members920,922 to an open orientation.
• Thetear strip970 is positioned through the centerline of the first andsecond housing members920,922. In accordance with a preferred embodiment, thetear strip970 is secured to the first andsecond housing members920,922 either through adhesive or other mechanical frangible, plastic coupling features. When pulled, thetear strip970 “tears” the center out from between the first andsecond housing members920,922 allowing thesuturing apparatus910 to fall open. Thetear strip970 may be a straight adhesive or molded strip, or thetear strip970 may include a camming feature (as discussed below) as part of the distal most end further spreading open the halves as it is removed.
• A further embodiment is disclosed with reference toFIGS. 25 and 26. This embodiment employs apull cable1070 to facilitate selective opening of thesuturing body1014 for release of a jammed needle therefrom. In accordance with this embodiment, thesuturing body1014 is composed of afirst housing member1020 andsecond housing member1022 making up asuture housing1024. The first andsecond housing members1020,1022 are hinged1072 along one end thereof (or are separate non-associated halves). The first andsecond housing members1020,1022 are further provided withlacing loops1074 along the open end thereof. Thelacing loops1074 are shaped and dimensioned to permit the placement of apull cable1070 therethrough in a manner which holds the first andsecond housing members1020,1022 together.
• More particularly, thepull cable1070 is laced through thelacing loops1074 alternately positioned on the first andsecond housing members1020,1022 much like the hinge of a door. As long as thepull cable1070 is present around the perimeter of the first andsecond housing members1020,1022, the first andsecond housing members1020,1022 are held together and the needle1028 is retained therein. However, when it is desirable to remove the needle1028 or otherwise open thesuturing body1014 of thesuturing apparatus1010, thepull cable1070 is pulled withdrawing it from thelacing loops1074 and releasing the first andsecond housing members1020,1022 from each other. With the first andsecond housing members1020,1022 released, the springbiased hinge1072 draws the first andsecond housing members1020,1022 apart by pivoting them along thehinge1072.
• Aspreader plate1170 embodiment is disclosed with reference toFIGS. 27 and 28. This is a variation on the tear strip design disclosed above with reference toFIGS. 23 and 24. In accordance with this embodiment, thecenter connection member1172 not only joins and releases the twohousing members1120,1122, but has acamming member1174 on the distal end of thecenter connection member1172 that as it is pulled through the system actually cams the first andsecond housing members1120,1122 apart not just allowing them to freely fall apart.
• More particularly, and as discussed above with the various other embodiments, the suturing body1114 includes afirst housing member1120 and asecond housing member1122 making up thesuture housing1124. The first andsecond housing members1120,1122 are hinged1176 along one end thereof, with aspring1178 biasing the first andsecond housing members1120,1122 to an open orientation (or are separate non-associated non-spring biased halves). Thecentral connection member1172 is positioned through the centerline of the first andsecond housing members1120,1122. In accordance with a preferred embodiment, thecentral connection member1172 is secured to the first andsecond housing members1120,1122 through a member that is rigid enough to prevent inadvertent deployment of the system but can be broken or disengaged from the distal end of thesuture housing1124. When pulled, thecentral connection member1172 releases the first andsecond housing member1120,1122 allowing thesuture housing1124 to fall open.
• The opening of the suturing body1114 upon removal of thecentral connection member1172 is facilitated by including acamming member1174 at the distal end1180 of thecentral connection member1172. Thecamming member1174 is positioned and shaped such that it extends between the first andsecond housing members1120,1122 in a manner pushing the first andsecond housing members1120,1122 apart for removal of the needle1128 or to provide other access to the internal structure of the suturing body1114.
• Referring toFIGS. 29, 30 and 31 yet a further embodiment of the present invention is disclosed. The embodiment employs a series of crushable interlocking clamps1270 in the selective opening of thesuturing body1214. As with the cam pin set, the interlocking clamps1270 hold the first andsecond housing members1220,1222 together during normal function. When acable1272 secured to the interlocking clamps1270 is pulled, the interlocking clamps1270 are crushed, unlocking the first andsecond housing members1220,1222 and allowing them to pivot open under the control of the springbiased hinge1274.
• In addition to the inclusion of a release structure for the housing structures described above, each of these embodiments is provided with a housing outer profile, shaped and dimensioned to permit limited closing of the suturing body as it is withdrawn from the stomach. In particular, the outer profile is rounded with a convex profile designed such that the first and second housing member are at least partially forced together when the suturing device is withdrawn through a trans-oral tube.
• With the convex profile in mind, it is contemplated it may be desirable to hinge the first and second housing members along their proximal ends (seeFIGS. 27 and 28). Either of the various release mechanism may be used in accordance with this embodiment. However, by positioning the hinge at the proximal end thereof the first and second housing members are directly connected to the shaft allowing them to be easily re-closed during extraction rather than having numerous loose parts free to move and fall wherever.
• One of the challenges of a suturing apparatus offering a needle that moves through a continuous circular path is to identify to the user where the needle is in the stroke of the device as well as give the user a method to stop at the end of one full stroke around before starting the next stroke. Current imaging techniques allow doctors to visualize a variety of endoscopic procedures. However, the techniques and devices must be designed to permit visualization. In addition, and where visualization is important to completion of the technique, it is important that physical feedback be combined with the visual feedback to ensure redundancy in the event visualization is not possible.
• As such, the present suturing apparatus is provided with a variety of indicators for both physical and visual identification of the procedure being performed. Briefly, and as will be discussed below in greater detail, the present endoscopic suturing device includes means for identifying the position of the needle along its path both locally in the surgical field and externally on the actuation mechanism. In addition, the endoscopic suturing device includes a secondary mechanism designed to stop the needle at the end of one full actuation to indicate to the user that it is the proper time in the sequence to re-position the device for subsequent actuations.
• More particularly, and in accordance with the various embodiments described below, the surgical suturing apparatus includes a suture housing and a needle mounted within the suture housing for movement about an arcuate path. A drive assembly operably associated with the needle for controlling movement of the needle with a suture secured thereto about the arcuate path in a manner facilitating application of the suture to tissue. A mechanism is provided for determining the position of at least one of the distal end of the needle and the proximal end of the needle at all points along the arcuate path about which the needle moves.
• Referring toFIG. 32, theendoscopic suturing device1610 includes aspring ball lock1670 shaped and dimensioned to provide a physical indication of theneedle1628 position. In accordance with a preferred embodiment, asmall ball bearing1672 isspring1674 biased into the path of the oncomingneedle1628 to stop its motion at the end of its travel. Theball bearing1672 is mounted within the suturing body1614 for access to and contact with the exterior surface of theneedle1628. Theball bearing1672 isspring1674 biased toward the exterior surface of theneedle1628. As such, when theneedle1628 is moved along its arcuate path and comes into contact with theball bearing1672, tactile feedback is provided to the user. Theneedle1628 is provided with arecess1676 along its exterior surface (preferably adjacent the tip of the needle, although multiple recesses may be employed at various locations along the length of the needle to provide physical indications of needle position). Therecess1676 is shaped and dimensioned to permit theball bearing1672 to seat therein when theneedle recess1676 comes into alignment with theball bearing1672 providing the user with tactile feedback of the needle positioned1628. In accordance with a preferred embodiment, theball bearing1672 is positioned adjacent the entry point for theneedle1628 as it begins its throw loop and therecess1676 of theneedle1628 is formed therealong at a position such that the operator is provided with additional tactile feedback that a complete needle loop is achieved.
• It is contemplated the ball bearing may be used in combination with a camming mechanism to move it out of the path for the next stroke to occur or it can be used at a restricting force that only applies feedback to the user that the end of a stroke has been achieved, but can be overcome by the user though the application of more force.
• In accordance with an alternate embodiment, and with reference toFIG. 33, a springratchet pawl lock1770 is oriented to interfere with movement of theneedle1728 for identifyingneedle1728 position and the completion of a needle loop. More particularly, a pawllock lever arm1772 is secured along the forward end of the needle path for contact with theneedle1728 in a manner providing a physical indication as to the position of theneedle1728. The pawllock lever arm1772 is secured along the forward end of the needle path for contact with theneedle1728 in a manner providing a physical indication. The pawllock lever arm1772 includes afirst end1774 andsecond end1776. Thefirst end1774 of thelever arm1772 is pivotally secured to the suturing body1714 of the suturing device1710. Thesecond end1776 oflever arm1772 extends toward and into contact with the exterior surface of theneedle1728. Thelever arm1772 is oriented such that when theneedle1728 is moved in a counter-clockwise direction, thelever arm1772 slides over the exterior surface of theneedle1728.
• However, and as with the prior embodiment, the exterior surface of theneedle1728 is provided with arecess1778 along its exterior surface. Therecess1778 is shaped and dimensioned to permit thesecond end1776 of thelever arm1772 to seat therein when theneedle recess1778 comes into alignment with thesecond end1776 of thelever arm1772. As mentioned above, and in accordance with a preferred embodiment, thelever arm1772 is positioned adjacent the entry point for theneedle1728 as it begins its throw loop and therecess1778 of theneedle1728 is formed therealong at a position such that the operator is provided with a tactile feedback that a complete needle loop is achieved.
• Referring toFIGS. 34, 35, 36 and 37, the suturing apparatus includes a pop-outindicator pin1870. Thepin1870 is shaped and dimensioned to pop out the side of thesuturing body1814 when theneedle1828 is in its advanced position giving the surgeon visible feedback as to theneedle1828 position within the surgical site of the endoscope. Once theneedle1828 is fully advanced, thepin1870 is spring biased to the hidden or in position indicating the suturing apparatus1810 is ready for repositioning (seeFIGS. 34 and 35). Visualization thereof is provided by coloring the exposedportion1871 of thepin1870 in a distinctive color to allow ready identification that theneedle1828 is positioned in a desired orientation.
• More particular, thepin1870 is spring biased within anaperture1872 formed in the wall of thesuturing body1814. Thepin1870 is biased to a hidden position and includes afirst end1876 and asecond end1878. Thefirst end1876 is positioned for contact with theneedle1828 as it moves along its arcuate path, while thesecond end1878 is positioned adjacent the outer surface of theaperture1872 for movement between a hidden position and an exposed position. With this in mind, thesecond end1878 of thepin1870 is colored in a distinctive manner allowing ready visualization thereof.
• Movement of thepin1870 is facilitated by the movement of theneedle1828 into contact with thefirst end1876 of thepin1870. In particular, thefirst end1876 of thepin1870 is seated within the path of theneedle1828, although it is shaped and dimensioned to readily move once theneedle1828 moves into contact therewith (without unduly interfering with the movement of the needle as it makes its arcuate path).
• In accordance with another embodiment and with reference toFIG. 38, theneedle1928 is colored to provide ready visualization thereof. More particularly, theneedle1928 is made with contrasting color to the surgical field to improve the visibility of the surgeon to identify where theneedle1928 is currently positioned. In accordance with a preferred embodiment, thetip1970 is colored with the contrasting color to provide a ready identification the needle is exiting the suturing body.
• Referring toFIG. 39, yet a further embodiment is disclosed. In accordance with this embodiment, theneedle2028 position is calibrated with anindicator2070 secured at the handle of thesuturing apparatus2010. It is contemplated theindicator2070 might be several hemispherical patterned lights, a dial indicator or other circular path indicator. In accordance with this embodiment, thesuturing body2014 is provided with one or multipleHall effect sensors2074 working in conjunction with theneedle2028 to provide the operator with an indication of theneedle2028 position. As the steel or magnetizedsteel needle2028 passes adjacent the threesensors2074 shown inFIG. 39 the system lights up the appropriate needle position indicator lights2070 on handle2072. Although Hall effect sensors are disclosed in accordance with a preferred embodiment of the present invention, other electronic means known to those skilled in the art could be used within the spirit of the present invention. For example, the sensors could be mechanical spring biased switches, or even extremely low voltage contact or inductance switches that make contact through needle itself making contact with both side of the switches (one placed on either side of the needle track).
• Improved functionality of the present suturing apparatus is achieved by the provision of a mechanical attachment mechanism specifically adapted for attaching the vacuum chamber and suturing body to the end of the endoscope, allowing for rotational positioning of the endoscopic suturing device with respect to the endoscope. The various embodiments described below provide for a mechanical attachment mechanism that attaches the vacuum chamber and suturing body at the end of the endoscope, allowing for flexible positioning of the vacuum chamber and suturing body away from the endoscope to increase visibility of the pocket. In accordance with one embodiment described below, the mechanical attachment mechanism includes a flexible connection arm that collapses against the endoscope during insertion for a low profile insertion, but then springs away from the endoscope once in the body to improve visibility of the vacuum chamber and suturing body for positioning and suture deployment.
• In accordance with another embodiment, the mechanical attachment mechanism attaches the vacuum chamber and suturing body to the end of the endoscope through the use of a detachable mechanism that can be removed and passed into a body cavity prior to the introduction of the endoscope, or for interchanging the suturing apparatus with another suturing body or even another endoscopic device. This could also allow for interchanging between a vacuum assist suture device and a non-assisted device.
• The mechanisms provide for a unique method for access to a body cavity through either a natural orifice or a surgical initiated orifice. In particular, the present invention provides a method for inserting a suturing apparatus, or other surgical instrument, through a body orifice. The instrument has a low profile orientation and a deployed orientation which is larger than the size of the body orifice through which it is to be inserted. The method is achieved by coupling the instrument to an endoscope and placing the instrument in its low profile orientation, inserting the endoscope and the instrument through a natural orifice to a target position within a body while the instrument is in its low profile orientation, and actuating the instrument to it is deployed orientation. Finally, the instrument is returned to its low profile orientation and withdrawn from the body through the natural orifice.
• Referring toFIG. 40, a first embodiment in accordance with the present invention is disclosed. In accordance with this embodiment, ascope attachment ring2170 is secured about thedistal end2172 of theendoscope2174 to which thepresent suturing apparatus2110 is to be mounted. Theattachment ring2170 generally includes aring body2176 havingparallel apertures2178,2180 respectively shaped for the receipt of theendoscope2174 and thesupport shaft2182 of thepresent suturing apparatus2110 to which thesuturing body2114 andvacuum chamber2146 are attached. With regard to theendoscope2174, thefirst aperture2178 is shaped for frictional engagement with the outer surface of theendoscope2174 in a manner preventing rotation of theattachment ring2170 relative to theendoscope2174.
• Thesecond aperture2180 is shaped and dimensioned for receiving theshaft2182 of thesuturing apparatus2110, and in accordance with a preferred embodiment thereof, thesecond aperture2180 is slightly larger than theshaft2182 of thesuturing apparatus2110. In this way, thesuturing apparatus2110 may be rotated relative to theendoscope2174 for improved access to tissue. Positioning of thesuturing apparatus2110 relative to theattachment ring2170 is achieved by positioningabutment members2184,2186 along theshaft2182 of thesuturing apparatus2110 on opposite sides of theattachment ring2170. Thesemembers2184,2186 can be coupled to theshaft2182 via screw threads during manufacturing, pressed into place during manufacturing or be molded as part of the attachment ring itself. In this way, thesuturing apparatus2110 may be freely rotated relative to theendoscope2174 while thesuturing apparatus2110 is substantially prevented from longitudinal movement relative thereto.
• In accordance with another embodiment and with reference toFIGS. 41, 42 and 43, anendoscope attachment ring2270 similar to that described above is secured about thedistal end2272 of theendoscope2274 to which thepresent suturing apparatus2210 is to be mounted. Theattachment ring2270 generally includes aring body2276 havingparallel apertures2278,2280 respectively shaped for the receipt of theendoscope2274 and the presentsuturing apparatus shaft2282. With regard to theendoscope2274, theaperture2278 is shaped for frictional engagement with the outer surface of theendoscope2274 in a manner preventing rotation of theattachment ring2270 relative to theendoscope2274.
• As for thesecond aperture2280 receiving theshaft2282 of thesuturing apparatus2210, and in accordance with a preferred embodiment thereof, thesecond aperture2280 is approximately the same size as theshaft2282 of thesuturing apparatus2210. In this way, thesuturing apparatus2210 is prevented from rotating relative to theendoscope2274 allowing for the elastic deployment off the axis of theendoscope2274 to permit better visualization. Positioning of thesuturing apparatus2210 relative to theattachment ring2270 is achieved by positioningabutment members2284,2286 along theshaft2282 of thesuturing apparatus2210 on opposite sides of theattachment ring2270. In an alternate embodiment the fit between the endoscope attachment ring and the elastic arm could be a loose fit as discussed above with regard to the embodiment shown inFIG. 40 permitting it to be freely rotated relative to the endoscope while the endoscopic suturing device is substantially prevented from longitudinal movement relative thereto.
• Improved access of the suturing apparatus is further facilitated by manufacturing theshaft2282 distal from thesecond aperture2280 of theattachment ring2270 from a flexible material that is biased to a position removed from theendoscope2274. In this way, thesuturing apparatus2210 may be held close to theendoscope2274 during insertion, reducing the profile of the structure being inserted trans-orally, while allowing for movement of thesuturing apparatus2210 away from theendoscope2274 when thesuturing apparatus2210 reaches its desired location.
• More particularly, the portion of theshaft2282aproviding for flexing of thesuturing body2214 away from theendoscope2274 is an elastomer lever arm designed to move thesuturing apparatus2210 off axis from theendoscope2274 in a manner improving visualization of thesuturing apparatus2210 and its usage while still allowing it to deflect against the endoscope during insertion and extraction, reducing its overall profile during these activities.
• In accordance with an alternate embodiment of the present invention and with reference toFIGS. 41aand 42a, theattachment ring2270amay be constructed with aconnection member2283aextending distally fromsecond aperture2280a. Theconnection member2283ais an elastomer lever arm designed to move thesuturing apparatus2210a, with theshaft2282athereof extending through theconnection member2283aoff axis from theendoscope2274ain a manner improving visualization of thesuturing apparatus2210 and its usage while still allowing it to deflect against theendoscope2274aduring insertion and extraction, reducing its overall profile during these activities.
• As briefly mention above, theconnection member2283ais shaped and dimensioned to fit about theshaft2282aof thesuturing apparatus2210a. Theconnection member2283ais constructed of a resilient material and is biased to a position removed from theendoscope2274a. In this way, theconnection member2283awith theshaft2282aof thesuturing apparatus2210 extending therethrough may be held close to theendoscope2274aduring insertion, reducing the profile of the structure being inserted trans-orally. However, once thesuturing body2214ais positioned within the body cavity, theconnection member2283ais released, allowing it to extend away from theendoscope2274a. Because theshaft2282aof thesuturing apparatus2210 is positioned within theconnection member2283a, theshaft2282aand thesuturing body2214aare moved away from theendoscope2274aas theconnection member2283amoves away from theendoscope2274a.
• In addition to the various embodiments discussed above and with reference toFIGS. 44, 45 and 46, it is contemplated aguidewire introducer2470 for asuturing apparatus2410 may be employed. Such a device is used in combination with a detachable vacuum chamber2446 and suturing body2414 detailed above. The distal end components, that is, the vacuum chamber2446 and the suturing body2414 are passed, for example, through the oral cavity in advance of the endoscope2472 and subsequently attached to the endoscope attachment ring2474 via aguide wire2470 which is pulled through a support shaft2476 in a manner drawing the suturing body2414 and vacuum chamber2446 onto the support shaft2476. The endoscope2472 itself can be used to advance the detached vacuum chamber2446 and a suturing body2414 down the oral cavity. Thepre-positioned guide wire2470 within the working channel of the endoscope2472 is terminated at its distal end2471 by connection to the vacuum chamber2446 and suturing body2414. Once passed into the stomach, the vacuum chamber2446 and suturing body2414 are pulled back into attachment to the distal end of the endoscope2472 and onto a support shaft2476 by pulling the suturing body2414 and vacuum chamber2446 into engagement with the endoscope2472 through the action of theguidewire2470 to which the vacuum chamber2446 and suturing body2414 are connected. This allows for use of a vacuum chamber2446 and suturing body2414 that are laterally and thickness wise larger than could be passed in fixed attachment to the endoscope during insertion.
• As an alternative embodiment, the vacuum chamber can be interchangeable used with non-vacuum equipment that looks similar or identical to the vacuum version, but does not utilize the vacuum to position the tissue and merely relies upon placing the chamber adjacent to the tissue to be sutured. This drastically reduces the bite size, but also reduces the possible trauma to the tissue that vacuuming the tissue into the pocket may cause.
• In particular, there are some procedures that would preferably be used without a vacuum assist to pull the tissue into the vacuum chamber, but rather would merely throw the suture with minimal tissue bite depth. There are even clinical situations where the vacuum could induce damage to the tissue. An interchangeable vacuum chamber that has a differing cavity depth and profile could be used with the suturing apparatus without a vacuum assist.
• A quick handle disconnect is also contemplated in accordance with present invention and is shown with reference toFIGS. 47, 48, 49, 50 and 51. This feature may be used in combination with or separately from the guidewire introducer as described above. Briefly, this embodiment employs asuture housing2524, aneedle2528 mounted within thesuture housing2524 for movement about an arcuate path, a drive assembly operably associated with theneedle2528 for controlling movement of theneedle2528 with a suture secured thereto about the arcuate path in a manner facilitating application of the suture to tissue, ahandle2570, an elongated flexible member, for example, adrive cable2542 having a distal end attached to thesuture housing2524 and a proximal end attached to thehandle2570, and a mechanism for releasing and reattaching thehandle2570 to theflexible member2542.
• The utilization of a quick handle disconnect facilitates distal detachment and pre-passing of thesuturing apparatus2510 through the selective attachment and detachment of thehandle2570 from theflexible drive cable2542 to which thesuturing body2514 andvacuum chamber2546 are connected. In accordance with this embodiment, thedrive cable2542 may function much like the guidewire previously discussed in allowing one to pass thesuturing body2514 and thevacuum chamber2546 into position prior to complete assembly. This improvement allows one to pre-pass thesuturing apparatus2510 from the distal end of the endoscope in manner reducing the required profile because thesuturing apparatus2510 is positioned distal of the endoscope during passage thereof rather than passing thesuturing apparatus2510 from the proximal end of the endoscope in a manner increasing the required passageway since the profile must accommodate both.
• More particularly, thehandle2570 is composed of ahandle body2574 in which thedrive cable2542 is releasably secured for actuation. With this in mind, thehandle body2574 includes acentral passageway2578 in which thedrive cable2542 is stored and mounted. Thehandle body2574 is composed of acentral grip2580 and aslide member2581 that moves relative to thecentral grip2580 in a manner discussed below in greater detail. Thecentral passageway2578 includes a firstopen end2582 and a secondclosed end2584. Adjacent the secondclosed end2584 is a spring loadedtrigger lock2586 secured to thecentral grip2580. Thetrigger lock2586 is shaped and dimensioned to engage a protrusion2594 (for example, a bullet nose tip) along theproximal tip2588 of thedrive cable2542. In this way, theproximal tip2588 of thedrive cable2542 is mounted within arecess2590 in theproximal end2592 of thepassageway2578 and within the central grip2580 (for centering thereof), and thetrigger lock2586 is moved downward into engagement with theprotrusion2594 for maintaining the drive cable2576 within thehandle body2574. When it is desired to remove thehandle2570 from thedrive cable2578, one need only actuate thetrigger lock2586 to its release position and thehandle body2574 may be freely removed from thedrive cable2542. Retention of thedrive cable2542 within thehandle body2574 is further facilitated by the inclusion of alocking slide2596 along theslide member2581. Thelocking slide2596 frictionally interacts with acollar2598 formed ondrive cable2542 for retention of thehandle body2574 thereon.
• In practice, the distal end of thedrive cable2542 is inserted within thepassageway2578 formed in theslide member2581. Thedrive cable2542 is inserted to such a point that thecollar2598 of the drive cable2576 is aligned withopenings2583 formed along theslide member2581. At this point, thelocking slide2596 is slid along theslide member2581 and is moved over thecollar2598 into engagement therewith. Thedrive cable2542 is, at this point, secured to theslide member2581. Theslide member2581 is then moved proximally relative to thecentral grip2580 until theproximal end2588 of thedrive cable2542 is seated within therecess2590 formed in thecentral grip2580. Thetrigger lock2586 is then spring actuated to engage theprotrusion2594 at theproximal tip2588 of thedrive cable2542 for securing it to thecentral grip2580 and thehandle body2574.
• Once thehandle2570 is secured to thedrive cable2542, release thereof is achieved by reversing the attachment steps discussed above. In particular, thetrigger lock2586 is rotated forward to permit release of theprotrusion2594 from within therecess2590 of thecentral grip2580.
• As discussed above, thepresent handle2570 allows for actuation of thedrive cable2542 in a manner operating thepresent suturing apparatus2510. In particular, relative movement of thecentral grip2580 and theslide member2581 while thedrive cable2542 is seated within thecentral grip2580 causes actuation thereof permitting the drive assembly to function in the manner described above.
• Although the selectively releasable connection is described above with reference to the handle of a suturing apparatus, it is contemplated the releasable connection could similar be applied in the selective connection of the suturing body to the shaft connecting the suturing body to the handle. In this way, one could selectively connect the suturing body to the shaft once the suturing body is positioned within the body cavity and ready for use in the application of a suture to tissue.
• The vacuum pressure available in different operating room suites varies greatly from location to location. Improvements to the vacuum chamber minimizing the necessary vacuum required have been discussed above. However, such structural changes might not be sufficient to ensure the present endoscopic suturing apparatus can be used in any location. The embodiments detailed herein are improvements to the handle to locally increase the vacuum in the vacuum chamber.
• Each of these embodiments provides an endoscopic instrument, for example, a suturing apparatus, adapted for use with an endoscope. The instrument includes an elongated tube having a distal end and a proximal end, an end effector, for example, the suturing body of the suturing apparatus, attached to the distal end of the elongated tube, and a handle attached to the proximal end. The handle includes a mechanism for attaching the instrument to a first vacuum source. The handle further includes a second vacuum source integral with the handle for amplifying the first vacuum source, whereby the first and second vacuum sources combine to operate the end effector.
• Referring toFIG. 64, this problem is addressed by the provision of a syringe based handle vacuum assistdevice2970. In accordance with a preferred embodiment of the present invention, asyringe mechanism2972 is placed in parallel to themain vacuum attachment2973 to thesuturing apparatus2910. This allows the normal operating room vacuum source to be used to accomplish as much as it is capable of and, if additional vacuum is still necessary to get a good tissue bite, thesyringe mechanism2972 can be pulled by the surgeon to increase the vacuum in thevacuum chamber2946. Since the normally available vacuum source of the operating room is the primary mechanism for drawing tissue into thevacuum chamber2946, the volume necessary in thesyringe mechanism2972 is minimized as the tissue will already be engaged in thevacuum chamber2946, although not to its full depth. An additional benefit of this method of assisting an operating room vacuum source is that fluids will have already been evacuated from thevacuum chamber2946 by the normal or primary operating room suction means and thesyringe mechanism2972 will not be filled with bodily fluids.
• In accordance with another embodiment, and with reference toFIGS. 65, abattery3071 powered multi-stroke vacuum assistdevice3070 for suction actuation is provided. Thevacuum assist device3070 includes a rotary fluid pump3072 (lobe pump, gear pump, peristalsis pump, etc.) to be used in a multi-stroke fashion to increase the maximum volume of gasses that can be extracted from the vacuum chamber after the primary vacuum source of the operating room is completely engaged. This has the same benefits of the syringe based system, but provides for the ability to exchange a greater volume of gas.
• Similarly, and with reference toFIG. 66, abattery3171 operateddisposable vacuum pump3170 is associated with a disposable deployment handle3172 used in conjunction with the present suturing apparatus3110. Like the mechanical multi-stroke mechanism detailed above, a battery operated, motor driven,disposable fluid pump3170 is included in thehandle3172 to supplement the vacuum available from the operating room.
• AlthoughFIGS. 65 and 66 disclose systems that are automatically actuated to create a secondary vacuum source,FIG. 67 discloses a trigger actuatedsystem3070a. Thetrigger3074aemploys trigger handles3076ain conjunction with agearing arrangement3078ato drive a fluid pump, for example, a singlelobe fluid pump3072a. As with the prior embodiments, actuation of thetrigger3074aand thefluid pump3072aincreases the maximum volume of gases that may be extracted from the vacuum chamber after the primary vacuum source of the operating room is completely engaged. This has the same benefits of the syringe based system and the automated system, but provides for manual actuation offering a surgeon greater control.
• It is further contemplated the vacuum assist may be created via a squeeze bulb with a one-way valve or a bellow mechanisms with a one-way valve or a secondary suction line. In addition, an idlingvane3172acould also be incorporated to intermittently provide vacuum assist (seeFIG. 68).
• As discussed above, visualization of thesuturing apparatus3510 is often critically important to the proper use thereof. With this in mind, thesuturing apparatus3510 may be modified to improve imaging thereof. In particular, theapparatus3510 includes aflexible member3516, for example, a support shaft or endoscope, having a distal end attached to asuturing body3514 for insertion of thesuturing body3514 through an orifice and into a body cavity. Thesuturing body3514 includes asuture housing3524 in which aneedle3528 and drive assembly are housed for movement of theneedle3528 with a suture secured thereto about an arcuate path facilitating application of the suture to tissue. A non-visiblespectrum sensing member3570 is associated with thesuturing body3514 for communicating a parameter of the procedure to avisual display3572. In accordance with a preferred embodiment, the non-visible spectrum sensing member is wirelessly linked to the visual display.
• For example, it is contemplated thesuturing apparatus3510 may be modified through implementation ofultrasonic transducers3570 in the suturing body3514 (seeFIGS. 83 and 84). Similarly, thesuturing apparatus3510 may be modified by the inclusion of a magnetic resonance imaging source transducer based within the suturing body or vacuum chamber to image the local suture site. Further, it is contemplated the endoscopic suturing device may be modified with the inclusion of an infrared based imaging sensor within the suturing body or vacuum chamber to evaluate blood flow to the sutured area post suture deployment or to identify blood rich areas in the interior lining pre-suture deployment for blood flow visualization. The endoscopic suturing device may also include Laser Doppler, oxygen, or carbon dioxide based sensors located within the suturing device to evaluate the blood flow characteristics before or after the suture line is deployed.
• These various visualization techniques provide for non-visible (outside the normal visible spectrum) imaging integrated into the suturing apparatus to improve the visualization of the site during suturing. As mentioned above, the contemplated mechanisms could be ultrasonic, infrared, MRI, Laser Doppler, oxygen and carbon dioxide sensors or other sensor system. In addition, the sensors provide for tissue penetration visualization means for viewing the location of surrounding organ geometry and Tissue penetration visualization means for viewing the suture deployment depth and bite size.
• Referring toFIG. 85 acartridge3670 for the loading ofneedles3628 andsutures3612 of different sizes is disclosed. In accordance with a preferred embodiment, areloadable cartridge3670 is capable of loadingdiffering size needles3628 and differing size sutures3612. Thecartridge3670 is shaped and dimensioned for ready attachment within thechannel3672 in which theneedle3628 is mounted in accordance with the embodiment disclosed. In particular, thesuturing body3614 is provided with acover3674 providing access to and closure of thechannel3672 in which theneedle3628 is located. Through the implementation of a cartridge based system thedetachable cartridge3670 can be removed and replaced with afresh needle3628 andsuture3612 or even a different size of needle or suture.
• In accordance with a preferred embodiment, theneedle3628 is supported in atrack member3676, which readily seats within thechannel3672 to create an assembly substantially similar to that disclosed above with reference toFIGS. 3 to 10.
• The cartridge based system may further be adapted to allow for the adjustment of the needle size through a simple cartridge replacement. In particular, and with reference toFIG. 86, thetrack3780 of thecartridge3770 is provided with aspacer wedge3782 taking up the space lost with the inclusion of a smaller needle3728. Thespacer wedge3782 is shaped and dimensioned to interact with thefriction camming member3738 in a manner allowing the suturing apparatus3710 to operate in accordance with this spirit of the present invention.
• While a cartridge based system is disclosed above, the suturing body of the suturing apparatus could be designed to permit simple replacement of the needle alone. Referring toFIGS. 87 and 88 this is achieved through the provision of anopenable suturing body3814. Rather than having a cartridge based reload, this embodiment for reloading merely controls theneedle3828 andsuture3812, making quick loading of a device without a removable section. Theneedle3828 would be coupled to thereloader3870 via aclamp3872 that could be released or easily broken and thesuture3812 would be maintained on thehandhold section3874 of thereloader3870. This would facilitate manipulation of theneedle3828 without touching it directly and would provide some form of suture management prior to being loaded into thesuturing apparatus3828.
• One of the difficulties in performing endoscopic procedures is efficiently and securely forming knots once the suturing is completed. It is desired the two ends, or leads, of the suture could be pulled tight simultaneously and a knotting element could then be used to tighten the adjacent ends. This would maximize the number of stitches that could be thrown before the suture needs to be cinched down since both ends of the suture could be pulled in a manner equally cinching from both ends of the suture.
• In accordance with a preferred embodiment of the present invention, a suture is secured by inserting the suture through a passageway into the body of a patient. The suture is then thrown into and back out of tissue. Finally a knot is tied along the length of suture in a manner securing the suture in place. The knot is then fused through the application of energy mechanically linking the first and second leads of the suture forming the knot. In accordance with a preferred embodiment, the term “fusing” is meant to refer to any technique by which the suture and/or knotting element are brought together in a manner whereby their material components are fixedly connected.
• In accordance with preferred embodiments of the present invention, tying of the knot is achieved in a variety of manners, wherein the first and second leads are entangled in a manner holding the leads relative to each other. As such, those skilled in the art will appreciate that a variety of knotting techniques may be used in accordance with the present invention. For example, a traditional tying technique may be used wherein the first and second leads of the suture are tied in a mechanical knot which is subsequently fused.
• In accordance with a preferred embodiment, and with reference toFIG. 62, asuture hooking device2710 is disclosed for tying first andsecond leads2730,2732 of a suture together. The hookingdevice2710 utilizes two parts to lock the suture together in a cap like fashion. The advantage to this method is that thecap2712 has twoextension arms2714,2716 that allow it to be twisted about its axis winding thesuture2718 mid-lengths onto its shaft. Thecap2712 would then be crushed into theoutside collar2720 locking the suture ends2718. This would allow for fine tensioning just prior to locking the suture together.
• More particularly, thesuture hooking device2710 includes anoutside collar2720 and acap2712 shaped and dimensioned to fit within theoutside collar2720. Theoutside collar2720 is generally cylindrical and includes an openupper edge2722 and aclose base2724. Thecap2712 includes anupper disk2726 and a downwardly dependingcentral shaft2728. Theupper disk2726 is shaped and dimensioned to fit within the openupper edge2722 of theoutside collar2720 such that it is frictionally retained therein. Thecentral shaft2728 is smaller and functions as a guide forsuture2718 wrapped thereabout.
• Thecap2712 further includes opposed downwardly extendingextension arms2714,2716. Thesearms2714,2716 provide for wrapping of thesuture2718 about thecap2712 upon rotation of thecap2712. Once thesuture2718 is wrapped about thecap2712, thedisk2726 is fixed within theoutside collar2720, securing thesuture2718 in a “knotted” arrangement.
• Although various mechanical knotting techniques are disclosed above, it is contemplated other fastening techniques may be used without departing from the spirit of the present invention. For example, and with reference toFIG. 63, fusing of the tied suture is preferably achieved by RF, ultrasonic, or electrocautery for melting ofsuture knot2810 to improve knot holding capability. This method would allow for a normal endoscopic knot to be tied adjacent the cinched tissue area. But since it would have a tendency to untie, an energy source (cautery, ultrasonic, RF, or other heat source) would then be applied to the knot fusing the knot together.
• The lacing pattern, the cinching method, and the anchoring means of the suture all contribute greatly to ease of use of the device. With this in mind, various suturing techniques have been developed. The present disclosure is meant to detail at least the preferred lacing method and an alternate anchoring method for cinching both ends simultaneously.
• In accordance with the various lacing technique described below, the present method is achieved by providing a suture with a needle attached thereto. The suture includes a first lead and a second lead. The needle and suture are then inserted into an organ through a passageway. A single stitch is thrown through a first tissue member and a single stitch is thrown through an opposed and spaced apart second tissue member. The step of throwing stitches is repeated at least once and the first and second tissue members are brought into contact by tensioning the suture, whereby suture drag is minimized during the tensioning and even tissue compression substantially achieved. Finally, the suture is secured in positioned with the first and second tissue members in apposition.
• In accordance with a first embodiment shown inFIG. 52, resistance to cinching of a stitchedsuture4212 is achieved via a throw reversing pin technique. The technique is initiated using traditional stitching techniques. That is, the needle andsuture4212 are inserted and alternating stitches are thrown alongopposed tissue members4274,4276. The stitches are consistently thrown in the proximal to distal direction, that is, the stitch is initiated by inserting the needle through the tissue proximally to the point at which the needle stitch is completed by reentering the tissue. Although the terms distally and proximally are used in the present description, those skilled in the art will appreciate that these terms are relative and ultimately the specific direction of stitching may be reversed without departing from the spirit of the present invention.
• However, thefinal throw4270 of the suture4212 (that is, the final loop or last stitch of the suture through the tissue) is altered to reduce friction during final cinching of thesuture4212. More particularly, and in accordance with a preferred embodiment of the present invention, drag and friction are reduced by positioning a reversingpin4272 between thesuture4212 and thetissue wall4274 after thelast stitch4270 is completed. This allows thesuture4212 to be cinched without it overlapping itself and twisting up. Such an arrangement will significantly reduce the friction necessary to overcome and cinch closed the lacing.
• In accordance with another embodiment, and with reference toFIG. 53, resistance to cinching of a stitched suture4312 is achieved via a throw reverse throw-over technique. The technique is initiated using traditional stitching techniques. That is, the needle and suture4312 are inserted and alternating stitches are thrown alongopposed tissue members4374,4376. The stitches are consistently thrown in the proximal to distal direction, that is, the stitch is initiated by inserting the needle through the tissue proximally to the point at which the needle stitch is completed by reentering the tissue. That is, the needle and suture4312 are inserted and alternating stitches are thrown along opposed tissue members. The stitches are consistently thrown in the proximal to distal direction, that is, the stitch is initiated by inserting the needle through the tissue proximally to the point at which the needle is stitch is completed by reentering the tissue. However, thefinal throw4370 of the suture4312 is reversed to reduce friction during final cinching of the suture; that is, thefinal throw4370 is completed by inserting the needle through the tissue in a direction distal to the point at which the needle stitch is completed by reentering the tissue.
• More particularly, thefinal stitch4370 is reversed in the direction in which it is thrown such that it is directed toward the position from which the surgeon will be pulling upon the suture line to cinch the suture4312. This allows the suture to be cinched without it overlapping itself and twisting up. Such an arrangement will significantly reduce the friction necessary to overcome and cinch closed the lacing.
• In accordance with an alternate embodiment, and with reference toFIG. 54, aninitial locking loop4470 is employed to enhance the ability of one to cinch thesuture4412 upon completion of the stitching. In particular, afirst lead4412aof thesuture4412 is anchored to the tissue along thefirst lead4412aof the suture line rather than needing to have both ends accessed by the user throughout the procedure. More particularly, the first lead, or leading end,4412aof the suture line is stitched and a portion thereof is anchored to the tissue. Thereafter the stitching is completed, with thefinal stitch4470 and the second lead, or trailing end,4412bof the suture line is accessed for cinching thereof. However, and in contrast to traditional cinching techniques, only thesecond lead4412bof the suture line need be pulled to cinch thesuture4412. As shown inFIGS. 52 and 53, such an initial locking may be employed with other lacing techniques within the spirit of the present invention.
• It is contemplated each set of sutures may be locally cinched before the next set is deployed from the suturing apparatus. This minimizes, but does not eliminate the need for the last stitch steps discussed above.
• As shown inFIGS. 55 to 61, the preceding techniques for lacing opposed tissue members may be expanded in various ways. For example, and with reference toFIG. 55, thesuture4512 may be applied inseparate segments4513 with the first andsecond ends4512a,4512bof eachsegment4513 anchored to respective first andsecond tissue members4574,4576. Thefirst end4512aof thesuture4512 is subsequently tensioned and tied off to cinch the suture. By using segments of stitches in this manner (and as discussed below in accordance with other embodiments), local cinching of each segment of stitches may be performed in a manner which may assist in improving the drawing of tissue together.
• Referring toFIG. 56, thesuture4612 may be applied inseparate segments4613 with the first andsecond ends4612a,4612bof thesuture4612 coupled via aknotting element4614. The first andsecond ends4612a,4612bare subsequently tensioned to cinch thesuture4612 and theknotting element4614 andsuture4612 are fused to secure the suture in position.
• With reference toFIG. 57, thesuture4712 is once again applied inseparate segments4713. Thefirst end4712aof thesuture4712 is provided with aloop4716 through which the remaining portion of thesuture4712 is passed to couple thefirst end4712aof thesuture4712 to afirst tissue member4774. As to thesecond end4712bof thesuture4712, it is secured via aknotting element4714 as discussed above. More particularly, thesecond end4712bis secured to theknotting element4714 with a looping structure composed of afirst loop4718 which is coupled to theknotting element4714 while a portion of thesecond end4712bpasses through thesecond tissue member4776 to form asecond loop4720, the end of which is also coupled to theknotting element4714. Thereafter, thesecond end4712bmay be tensioned, in particular, thefirst loop4718 may be drawn through theknotting element4714 and theknotting element4714 and suture4710 are fused to secure the suture4710 in position.
• With reference toFIG. 58, thesuture4812 is applied inseparate segments4813 with the first andsecond ends4812a,4812bof thesuture4812 coupled via aknotting element4814. However, thefinal throw4870 of thesuture4812 is reversed as discussed above with regard toFIGS. 53 and 54. The first andsecond ends4812a,4812bare subsequently tensioned to cinch thesuture4812 and theknotting element4814 andsuture4812 are fused to secure thesuture4812 in position.
• Referring toFIG. 59, thesuture4912 may be applied inseparate segments4913 with the first andsecond ends4912a,4912bof eachsegment4913 anchored to respective first andsecond tissue members4974,4976. However, each throw of thesuture4912 is reversed as discussed above with regard toFIGS. 53 and 54, and extends in a distal to proximal direction as the suture is applied in the distal direction. Thefirst end4912aof thesuture4912 is subsequently tensioned and tied off to cinch thesuture4912. Referring toFIG. 60, the same lacing technique is applied with the exception it is not completed in segments.
• As shown inFIG. 61, anoverhand knot5022 may be used to secure thesecond end5012bof thesuture5012, while thefirst end5012aof thesuture5012 is anchored to the tissue.
• In accordance with the present invention, it is preferred to apply medical fluid/sealant for improving the suture lines ability to engage and retain the tissue. Particular, the suture line is subjected to substantial strain for a short period of time after its application while the tissue applies substantial tension in its attempt to retain to its original configuration. This generally lasts for 7-10 days after the surgery is completed, and it is during this time period in which potential suture breaks are more likely. With this in mind, and as the following embodiments disclose, an adhesive, sealant, or medical fluid delivery mechanism can be used in conjunction with the present suturing device to increase the short term strength of the stomach pouch by adhesively binding the opposed tissue. A method of deployment of sealants or other medical fluid changes the stiffness properties of the tissue to improve the suture strength of the gastroplasty by adhesively binding the opposed tissue.
• As such, and in accordance with a preferred embodiment of the present invention shown inFIG. 69, adhesive3210 is used to improve short term strength of the suture line3213, that is, the line of tissue held together via thesuture3212. A fluid deploying mechanism is utilized to lay down a line of fluid sealant or adhesive3210 along thesuture line3214 after thesuture line3214 is completed to improve holding strength of the line. Either a thin layer adhesive or a foaming (void filling) adhesive orsealant3210 can be used in conjunction with thesuture3212.
• In accordance with an alternate embodiment, and with reference toFIGS. 70, 71 and 72, thesuture3312 is a hollow tube suture withperiodic perforations3314 along its length. Once thesuture line3313 is finished, thesuture3312 would be pumped full of the sealant or adhesive3314 allowing it to be distributed all along its length increasing both the effective diameter of the suture, minimizing suture migration as well as providing a complimentary adhesive bond of the tissue together in addition to thesuture line3313.
• Referring toFIGS. 73 to 82, yet a further embodiment is disclosed. Aliquid polymer extrusion3350 is used to form asleeve3352 around theinternal pouch3353 formed in, for example, thestomach3354. The entire inside of the small gastroplasy createdpouch3353 and some length of the intestines would be coated with the polymer/adhesive3350. This not only improves the strength of the pouch suture line, it also potentially creates some form of malabsorption compliment to the procedure that improves weight loss.
• More particularly, and with reference to the various figures, a suction andapplication device3356 is first transorally inserted within thestomach3354. A vacuum is then created drawing opposedtissue surfaces3358,3360 together as shown inFIGS. 72 and 73. Thereafter, theliquid polymer extrusion3350 is applied to theopposed tissue surfaces3358,3360 while the vacuum continues to be applied in a manner keeping thewalls3358,3360 of thestomach3354 in apposition. Eventually, theliquid polymer extrusion3350 will cure holding the apposedtissue walls3358,3360 in apposition. Thereafter, and with reference toFIGS. 78 and 79, the suction andapplication device3356 in accordance with the present invention may be withdrawn and the internal profile of thestomach3354 is reduced to a simple passageway extending therethrough with a substantial portion of the stomach closed off from food absorption. Although the process described above does not employ sutures, the pouch could certainly be formed with suturing of the opposed tissue with the subsequent application of adhesives as described above.
• While the preferred embodiments have been shown and described, it will be understood that there is no intent to limit the invention by such disclosure, but rather, is intended to cover all modifications and alternate constructions falling within the spirit and scope of the invention.

Claims (20)

1. A method for suture lacing, comprising:

a. providing a suture with a needle attached thereto;

b. inserting the needle and suture into an organ through a passageway;

c. throwing a single stitch through a first tissue member, throwing a single stitch through an opposed and spaced apart second tissue member;

d. repeating step (c) at least once;

e. bringing the first and second tissue members in contact by tensioning the suture, whereby suture drag is minimized during the tensioning and even tissue compression substantially achieved; and

f. securing the suture.

2. The method according toclaim 1, wherein the suture includes first and second leads, and the step of securing includes knotting the first and second leads of the suture.

3. The method according toclaim 1, wherein the suture includes first and second leads and the step of securing includes anchoring at least one of the first and second leads of the suture to tissue.

4. The method according toclaim 3, wherein the step of securing includes anchoring both the first and second leads of the suture to tissue.

5. The method according toclaim 1, wherein the step of inserting includes insertion through a natural orifice of a patient.

6. The method according toclaim 5, wherein the step of inserting includes insertion through an orifice from approximately 3 mm to approximately 24 mm in diameter.

7. The method according toclaim 1, wherein the step of inserting includes insertion through a trocar.

8. The method according toclaim 7, wherein the step of inserting includes insertion through an orifice from approximately 3 mm to approximately 18 mm in diameter.

9. The method according toclaim 1, further including a step of reversing the direction of a final suture throw.

10. The method according toclaim 1, wherein the step of reversing includes positioning a reversing pin between the suture and either the first tissue member or the second tissue member.

11. A method for suture lacing, comprising:

inserting a needle with a suture secured thereto through a passageway;

alternately throwing the suture through a first tissue member and an opposed second tissue member;

reversing the direction of the final suture throw; and

securing the suture.

12. The method according toclaim 11, wherein the suture includes first and second leads and the step of securing includes knotting the first and second leads of the suture.

13. The method according toclaim 11, wherein the suture includes first and second leads and the step of securing includes anchoring at least one of the first and second leads of the suture to tissue.

14. The method according toclaim 13, wherein the step of securing includes anchoring both the first and second leads of the suture to tissue.

15. A method for suture lacing, comprising:

inserting a needle with a suture secured thereto through a passageway, wherein the suture includes a first lead and a second lead;

anchoring the first lead of the suture to a first tissue member;

alternately throwing the suture through a first tissue member and an opposed second tissue member; and

securing the suture.

16. The method according toclaim 15, further including a step of reversing the direction of a final suture throw.

17. The method according toclaim 16, wherein the step of reversing includes positioning a reversing pin between the suture and either the first tissue member or the second tissue member.

18. The method according toclaim 15, further including the step of anchoring the second lead to either the first tissue member or the second tissue member.

19. The method according toclaim 15, wherein the step of inserting includes insertion through a natural orifice of a patient.

20. The method according toclaim 15, wherein the step of inserting includes insertion through a trocar.

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